Open access peer-reviewed chapter

Agro-Industrial Waste Management: The Circular and Bioeconomic Perspective

Written By

Cosmas Chikezie Ogbu and Stephen Nnaemeka Okey

Submitted: 04 November 2022 Reviewed: 28 November 2022 Published: 08 February 2023

DOI: 10.5772/intechopen.109181

From the Edited Volume

Agricultural Waste - New Insights

Edited by Fiaz Ahmad and Muhammad Sultan

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Abstract

Traditional agricultural production is circular. Virtually no waste is produced. Residues are returned to soil as compost; used as bedding material in livestock husbandry (and returned to soil as compost) or as feed to produce animal protein and manure; utilized as construction materials; or fuel for domestic energy. Circular agricultural production ensures soil conservation, waste reduction, residues reuse, and recycling. The ever rising global population, and demand for food and agro-industrial products, necessitated a transition to linear agricultural production which generates enormous quantities of agricultural residues, agro-industrial, and food wastes. The economic losses, environmental degradation, and health hazards resulting from poor management of excess wastes, and their mitigation have been the subject of research and policy efforts at continental and regional levels. Current waste management models redirect attention to circular agricultural production and bioeconomic approaches aimed at waste reduction, reuse, and recycling. Such approaches view agricultural wastes as raw materials with economic benefits for the farmer, consumer, and investor in varied industrial enterprises (crop and animal production, animal and human health, food, beverage, neutraceutical, pharmaceutical, cosmetics, and material industries). The present review attempts to collate information on global production, and possible valorization of recyclable agro-industrial residues and food wastes.

Keywords

  • wastes
  • theoretical and technical availability
  • valorization
  • bioactive compounds
  • value-added products

1. Introduction

Agro-industrial wastes are inedible materials produced as a result of various agricultural and agro-industrial operations. They include wastes from slaughterhouses and meat processing, animal dung or manure, field crop wastes, crop residues, harvest wastes, and wastes from food consumption and processing [1, 2]. The huge diversity characteristic of the agricultural and livestock sectors means that very large and heterogeneous products end up as wastes. There are hence several types of agro-industrial wastes based on material composition and management.

1.1 Types of agro-industrial wastes

Agro-industrial wastes can be divided into three broad categories, namely recyclable and compostable or naturally occurring agricultural and agro-industrial wastes, non-recyclable and non-compostable agricultural and agro-industrial wastes, and hazardous agricultural and agro-industrial wastes. Compostable wastes are recyclable wastes, which can be reused in the farm or recycled in recycling plants. Some such as pruning, straw, leaves, stover, stalk, bagasse, cob, and animal dung or manure are regarded as primary residues because they arise directly from crop and animal production activities while others such as pit, shell, peels, husk, cake, slurry, and slaughterhouse wastes are regarded as secondary wastes because they arise from agro-allied industrial processing [1]. Generally, primary and secondary residues are categorized as least problematic in management. Non-recyclable agro-industrial wastes are wastes that result from farm construction operations, farm mechanization, transport, and livestock protection facilities. They are the most problematic to manage since they are usually bulky and not reused or recycled on-farm. They include plastic sheets and containers, metal containers and equipment, tires, shadings or anti-stone nests, machinery, metal structures for fences or covers, and irrigation facilities. Hazardous agro-industrial wastes are wastes that pose very serious immediate and remote problems if not correctly managed. They include phytosanitary products, chemical containers, acids, fertilizers, waste water, chemical contaminated water, foods, and other materials; medicines, agro-chemicals, and detergents. These wastes are managed following laid down regulations from the appropriate authorities. In this review we focus on the utilization of recyclable (primary and secondary) agro-industrial wastes (agro-industrial residue) (Figure 1) for the production of renewable energy and functional products for household, environmental, industrial, medical, veterinary, and animal production applications.

Figure 1.

Classification of recyclable agro-industrial wastes. Source: Sadh et al. [3].

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2. Global availability and estimates of agro-industrial residue biomass

Agriculture-based industries produce vast amounts of recyclable residues and wastes [3]. Food production, transportation, storage, processing, distribution, and consumption yield enormous wastes such as crop residues, food wastes, animal manure, animal wastes, and by-products, and forestry waste biomass. For instance, juice industries produce huge amounts of wastes such as peels, pulp, and drupes [4]; beverage industries produce cocoa, and coffee pulp, pod, and stalk as wastes; processing of cereals, canes, and grains yields husks, bran, bagasse, and molasses; nuts yield shells, cakes, and slurry following oil extraction; palm fruit processing yields large quantities of empty palm fruit bunch, palm fruit fiber, and palm oil sludge; processing of palm kernel yield shells while extraction of palm kernel oil yields palm kernel cake; meat industries produce trimmings, bone, offal, feather, hair or fur, cartilage, and blood [1, 2, 3]. From the growth of crops, various kinds of primary residues and wastes, namely stalk, stover, straw, leaves, stem, bagasse, and cobs are produced [13]. Raising of livestock and poultry in large confined feeding operations produces nearly unmanageable concentrations of dung or manure and slurry in addition to various slaughterhouse wastes [1, 2].

Global agricultural residue potential is rendered in terms of technical, theoretical, economic, and sustainable potentials [5, 6]. The theoretic potential gives the gross quantity of biomass potentially produced [7] while the technical potential is the fraction of the theoretical potential technically recoverable allowing for economic, social, environmental, and political constraints [6, 8]. The economic potential indicates the fraction of the theoretical and technical potential available for purchase as source of revenue to the producer. Globally, approximately 147.2 million metric tons (Mt) of fiber sources are theoretically available while 709.2 and 673.3 Mt of wheat straw and rice straw residues were estimated, respectively, in 1994 [3, 9]. Residues from cereals and sugar cane production account for 80% of the total residue from crops and constitute the most harvestable biomass [1, 10, 11]. Cho et al. [12] estimated global annual rice straw, wheat straw, corn straw, sugarcane bagasse, and rice husk production at 731, 354, 204, 181, 110 Mt, respectively, while wood biomass waste was put at 4.6 Gt yr−1. Wastes from coffee and olive oil industries were estimated at 7.4 and 30 Mt yr−1, respectively. Capanoglu et al. [13] indicated that close to 1.3 billion tons of food (about one-third of food produced) is lost as wastes before or after reaching the consumer.

Country-specific estimates of agro-industrial and food waste biomass production and availability are scanty and very patchy since very few countries consistently track (document) residue and waste production and use [1]. Thus, reported statistics are results of modeling studies mostly based on national crop production, crop yield, residue-to-product ratio (RPR), area under cultivation, and moisture content [7]. Reports from a number of such studies estimate on a global level an appropriation (including for energy) of 2.9 billion tons yr−1 (66% of total annual production) [11415]. A 2006–2008 estimate of crop residue production from barley, maize, rice, soybean, sugar cane, and wheat gave 3.7 + 1.3 or – 1.0 Pg (billion tons) accounting for ¾ of total production [16]. Regions outstanding include North and South America, Eastern and Southern Asia, with a production of more than 500 Tg (Mt) yr−1 each. South-east Asia and Eastern Europe have estimated value of 200 Tg yr−1 each [16]. Earlier estimates include 3.5–4.0 Pg yr−1 in the 1990s with cereals, sugar crops, and oil crops accounting for 79% of the total [17], 3.4 Pg yr−1 in 1991, and 3.8 Pg yr−1 in 2001 with cereals accounting for 74–75% [10], 4.4 Pg yr−1 in 2000 [14], and 5.4 Pg yr−1 for 1997–2006 using crop-specific harvest indices as estimator instead of RPR [18]. Using agricultural production data from FAO [19], Cooper and Laing [20] quantified crop residues and animal wastes produced on the African continent. The authors indicated that crop residues were mainly from coconut, maize, rice, and sugarcane production. Overall, 639,600 tons of coconut husks and 191,880 tons of coconut shells were estimated. Major producers were Tanzania (140,000 and 42,000 tons, respectively), Ghana (122,000 and 36,600 tons, respectively), and Mozambique (120,000 and 36,000 tons, respectively). Residues from maize were 16,296,301 tons of cobs and 90,602,879 tons of stalks with major production from South Africa (SA) (3,981,199, and 22,134,353 tons, respectively), Egypt (2,405,371 and 13,373,188 tons, respectively), and Nigeria (2,059,759, and 11,451,685 tons, respectively). A total of 22,858,042 tons of sugar cane residues were estimated with SA (6,302,133 tons), Egypt (4,112,925 tons), and Mauritius (1,443,750 tons) leading other countries in the continent. For the USA, the “Billion ton annual supply study” [21] and its update [22] reported an annual crop residue production of 550 Million dry ton matter(Mdt) yr−1; a more recent study reported 518 Mdt yr−1 [23] with 5.6 Mt (1% of total) corn stover appropriated for energy production [16, 23]. The US DOE [24] project estimated that approximately 144 Mt of primary agricultural residues are in use in diverse applications across the United States made up majorly of corn stover and concentrated in the Midwest regions, including the states of Illinois, Indiana, Iowa, Kansas, Minnesota, Missouri, Nebraska, Ohio, and South Dakota. Kim and Dale [25] had reported that corn production yielded roughly 10 Mt of grain ha−1 and approximately the same amount of stover (assuming a 1:1 crop:residue ratio). An estimate of US biomass resources in terms of economic potentials gave 94 Mt at $66 ton−1 coming from barley straw, corn stover, oats straw, sorghum stubble, and wheat straw with an increase between 158 and 180 Mt by 2040 [1, 24]. For Canada, about 48 Mt of dry agricultural crop residue is possible baring such factors as crop yield, cost of production, collection and transport, properties of residues, distance to processing facilities, the profit potentials of targeted use, and the degree of substitutability of other feedstock [1]. Bloomberg [26] had projected the potential supply of agricultural residues (80% grain straw) in the EU to be approximately 170 Mt at an average supply cost of €67 ton−1 while de Wit and Faaij [27] projected approximately 200 Mt at plant gate cost of €51 ton−1. Generally, the cost of crop production, crop yield, cost of residue harvesting, and the supply chain from point of collection to point of processing significantly impact price of residue. For Denmark, Energinet.dk [28] projected 1.0–1.5 Mt yr−1 while annual production of crop residues in Canada over the period 2001–2010 was estimated at 82 Mdt [29]. Ji [30] assessed the potential lignocellulosic biomass or crop residues feedstock in China for biofuel production and found a theoretical amount of 930.8 Mt. In Iran, Alavijeh and Yaghmaei [31] reported 11.33 Mt. Pradhan and Mbowa [32] had stated that availability of reliable feedstock data for biofuel production in SA is a challenge. Barahira et al. [33], however, estimated an annual crop residue production of ~43 Mt in SA with ~32 Mt from grains and ~6 Mt from sugar cane. Other estimates include residue from oil crops (groundnut, soybean, sunflower) (~3 Mt), vegetable crops (potato, tomato, cabbage) (~1 Mt), and other minor crops (~0.8 Mt). Residue from maize ranked first among all crops with ~28 Mt followed by sugar cane, wheat (~3 Mt), sunflower (~2 Mt), and soybean (~1 Mt) [33]. Batridzirai et al. [7] had reported the gross (above ground) crop residue potential from maize and wheat in SA as 14.4 Mt yr−1, but only 6.0 Mt yr−1 can be removed sustainably from the field. Regions in SA with the highest potentials for residue production include Northern Cape, Mpumalanga, and Free-state accounting for 87% of national residue potential. Maize stover is the predominant crop residue accounting for 90% of the current and future total residue potential. In India, about 500–550 Mt of agro-industrial residues are generated per year [34, 35, 36]. Agriculture alone generates 140 Mt yr−1 of biomass [34]. Cereals lead (352 Mt, 70%), fiber (66 Mt, 13%), oil seeds (29 Mt), pulses (13 Mt), and sugar cane (12 Mt, 2%). Of the 70% by cereals, rice has 34%, wheat 22% [37]. For fiber, cotton leads (53 Mt, 11% of crop residues) followed by coconut (12 Mt) [37]. FAO [38] reported an estimated total crop residue production of 95 Mt yr−1 for member states of the Union économique et monétaireouest-africaine (West African Economic and Monetary Union) (Benin, Burkina Faso, Côte d’Ivoire, Guinea-Bissau, Mali, Niger, Senegal and Togo) in 2010 with cereal straw accounting for 80 Mt yr−1 and straw from millet and sorghum ranking highest. Sahelian countries (Niger, Burkina Faso, Mali, and Senegal) had the largest share (96%) of crop residues especially cereal residues. Residues (peels) from tuber crops (yam and cassava) were estimated at 6 Mt yr−1 and came mostly from sub-humid countries (Cote d’ Ivoire and Southern part of Benin). Agro-industrial by-products include cotton cake (2 Mt yr−1 in 2005 but 1.34 Mt yr−1 in 2009), groundnut cake (2.5 Mt yr−1 in 2009), cereal bran (millet: 1.5–1.8 Mt yr−1; sorghum: 1.3 Mt yr−1), and molasses (100,000 tons yr−1) with Cote d’ Ivoire and Senegal accounting for 45 and 15% of the total, respectively. In Nigeria, agro-industrial residues result from crop and animal farming, crop and animal processing, and forestry and timber production [39]. Major crop residues are from cassava, yam, potatoes, fruits and vegetables, plantain, cocoa, coconut, coffee, cowpea, groundnut, maize, millet, rice, sorghum, sugar cane, wheat, soybean, and oil palm [39, 40]. Agba et al. [41] reported that the biomass potential of Nigeria as at 2005 stood at 13 million hectares of fuel wood, 61 Mt yr−1 of animal waste, and 83 Mt yr−1 of crop residues. From 10 crops, Simonyan and Fasina [42] estimated crop residue availability of 145.6 Mt yr−1 while Isola et al. [43] and Okeh et al. [44] reported 227,500 tons day−1 of animal manure. The annual production of agricultural wastes is this high because about 94% and 68% of households are engaged in crop and livestock farming, respectively [45]. In a study that evaluated global production of endocarp tissue from horticultural fruit crops, particularly drupes, as residue for biofuel production, Mendu et al. [4] reported an estimate of 2.4 × 107 tons consistent with FAO’s 3.1 × 107 tons (29% variation). The study reported greatest density of drupe endocarp production in developing countries in South Asia and broad lower-density distribution across Southern and Northern Europe and the Middle East. Isolated productions were mapped to USA, Africa, China, Australia, Central America, and South America. Highest endocarp yield was from coconut and mango (1.31 × 107 and 3.99 × 106 tons, respectively), which together accounted for 72% of total global drupe endocarp production [4]. Smil [17] had indicated that over 60% of global crop residues are produced in low-income countries, and almost 45% of residues come from the tropics. This is despite considerable regional differences in fraction of residue harvested and used (29% in sub-Saharan Africa and 90% in Western Europe) [14].

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3. Management of agro-industrial residues: the circular agricultural and bioeconomy perspectives

Traditional (subsistence) agriculture is based on circular sustainability model, which ensures practically nil waste as residues are recycled or used for various purposes including maintenance of soil fertility [46, 47]. Rise in global population, however, necessitated the intensification of agricultural production, linear-agricultural production system, globalization of food distribution, extensive storage, and agro-industrial processing, all of which generate extensive quantities and varieties of agro-industrial and food wastes [47, 48]. Previously considered of little or no economic value, harvest leftovers, crop residues, animal wastes (bones, carcasses, blood, fat, feathers, hair, cartilages, skins, viscera, and dung), and food wastes (household, food service, and retail wastes) are today viewed as valuable resources of significant economic value such that they have become co-products or raw materials from agro-industrial processing, crop, forestry, and animal production [49]. In the traditional circular agricultural model, farmer’s decision on agricultural residue use reflects their needs and preferences [50], and access to and affordability of alternative biomass resources determine the opportunity costs for a farmer or household to sell, use, or replace residues [50]. From time, agricultural waste biomass has fulfilled vital roles including livestock feed, animal bedding material, domestic fuel, construction material, some cash through sales, and maintenance of soil fertility [50, 51, 52]. Today, the huge excess residues and wastes after fulfilling these traditional roles are disposed by burning; a practice viewed by farmers as the most convenient, cheap with regard to time, labor, and finance, and beneficial for control of weeds, crop pests, and diseases (Figure 2) [52, 53, 54]. The traditional agricultural residue management models, however, have poor economic returns to the farmer, and poor soil health conservation and maintenance [52]. In addition, burning of agricultural residues has tremendous negative environmental implications including loss of soil nutrients, soil erosion, and release of climate pollutants including greenhouse gasses [48, 52, 55, 56, 57, 58, 59, 60]. Added to these are considerable adverse human and animal health concerns (Figure 2) [59, 60, 61].

Figure 2.

Impact of crop residue burning (CRB) [52].

Current agricultural residue and waste management models (the circular and bioeconomy models) (Figures 3 and 4) emphasize profitability, sustainability, technical feasibility, and adoption potential. That is, an integrated circular and bioeconomy approach that is sustainable, up scalable, crop- and region-specific, socially inclusive, environmentally sound, and technically robust [52]. The approach further harnesses the synergies existing among alternative options, aims at mitigating climate change, and contributes to achievement of sustainable development goals [52].

Figure 3.

Crop residue management: A paradigm shift from the traditional approach to agricultural bioeconomy and circular economy [52].

Figure 4.

Crop residue management intervention: Bioeconomy and circular economy perspectives [52].

This perspective is hence driven by the urge for better human and animal health and welfare, sustainable agricultural and animal production, the need to decarbonize the agricultural economy, exploitation of emerging opportunities through waste valorization and production of value-added products, to end waste burning and derive optimal economic benefits from agricultural residues and food wastes for improved livelihood, circularity in agricultural production system for example through reuse and recycling of residues, and the need to mitigate climate change (Figure 5) [52, 62].

Figure 5.

Mapping of benefits from bioeconomy-driven crop residue management. CA: conservation agriculture; CSA: climate smart agriculture; C: composting; BF: biofuel; BP: biochar production; BG, biogas; MP: mushroom production [52]. Numbers represent targeted sustainable development goals (SDGs).

The circular and bioeconomy approaches have become critical in the backdrop of declining soil fertility, and productivity, need of food and nutritional security, carbon sustainability, and to mitigate adverse health effects and greenhouse gas emission [52, 62]. Key components of the agricultural circular and bioeconomy waste management interventions are conservation agriculture, in situ crop residue incorporation, biomass energy production, biofuel generation, biochar and activated carbon production, residue composting and biofertilizer production, and substrate for edible fungi cultivation [52, 63, 64, 65, 66], production of materials such as packagings, food coatings, biopesticides, single cell proteins, and animal proteins [13, 67], and extraction of bioactive molecules and functional groups for varied applications [4748, 67]. Obviously, the potential availability and sustainability of feedstock supply for particular industry would depend on alternative or competing uses, cost of production and supply, crop yield and revenue from crops to farmers, and scale of crop farming enterprise [1, 11, 68]. Following is a review of application and allocation of agro-industrial residues (crop residues, fruits and vegetable wastes, animal manure, carcasses, and dairy wastes) and food wastes to major competing applications.

3.1 Application of agro-industrial wastes to soil conservation, soil erosion control, and maintenance of soil fertility

Soil conservation and enrichment are among the traditional and modern applications of crop residues and recyclable agro-industrial wastes including animal manure. It is a vital component of conservation agriculture. Traditionally, some quantities of crop residues are left on-farm to consciously or inadvertently prevent or minimize soil erosion, increase soil organic matter, maintain soil organic carbon, improve soil structure, conserve soil moisture, recycle plant nutrients, maintain soil organisms and microbial population, and maintain soil fertility while some proportions are composted or converted to bio-fertilizer for soil enrichment [7, 33, 69]. The circular and bioeconomy models further recommend in situ crop residue incorporation and no- or minimal-till cultivation practices. In China, it is estimated that 15% of annual residues production are converted to fertilizer while 31% are left on-farm [37, 70]. Wang et al. [71] had reported that crop residue use as fertilizer in Henan Province of China is made up of straw left in field, straw returned to field, straw chipping and mulching in field, quick composting in field, straw pile fermentation returned to field, straw-produced organic fertilizer, straw-produced ammoniation, and straw-produced silage. It is reported that in 2009, 15.4 Mt of wheat straw and 9.7 Mt of rice straw were used for fertilizer in China [72]. Also, crop residues accounted for 12–19% of total organic fertilizer resources [73], provided about 25–35% N, P, and K nutrients, and improved nutrient recycling in the soil. Batidzirai et al. [7] reported that in South Africa, out of a gross amount of 16 Mt yr−1 of maize stover, 6.3 Mt are below ground level and serve for soil organic carbon maintenance while 4.2 Mt is required for soil erosion control. Similarly, out of 1.8 Mt of wheat straw, 970,000 tons that are below the ground serve for soil organic carbon maintenance. In a study of the pattern of residue biomass use in cereal-sheep production system of North Africa, Ameur et al. [69] reported that 70.4% of farmers in Tunisia retain below 200 kg of crop residue per hectare (ha−1), 15.1% retain between 200 and 500 kg ha−1, while only 14.5% retain > 500 kg ha−1 as mulch. Baudron et al. [74] had reported that only 3% of farmers in Ethiopian Rift Valley retain more than 1 t ha−1 of crop residues on the farm. A number of studies [50, 69, 74, 75] have highlighted the challenges associated with crop residue allocation to competing applications including soil conservation in conservation agriculture and in crop-livestock integrated systems. Generally, the quantity of crop residue retained for soil conservation in integrated crop-livestock systems depends on scale of farming (acreage), type of crop, stocking density of livestock, share of livestock income, and crop yield, among other drivers of crop residue management [69].

3.2 Agro-industrial wastes for livestock production (feed and bedding material)

Historically, crop residues were used as animal bedding [11] and as supplemental feed for livestock especially in smallholder mixed agricultural systems. Erenstein [76] had observed that crop residues represent a fundamental resource for crop-livestock integration and intensification, along a broad range of smallholder mixed systems. In tropical and subtropical countries, food wastes serve as food for pet animals and feed for monogastric animals especially pigs. Agricultural biomass is a vital dry season feed resource, providing livestock feed when other resources are scarce. Valbuena et al. [50] stated that in semi-arid and arid areas, crop residue is a vital feed resource for livestock production, and there is increasing demand of agricultural biomass for animal feeding due to low availability of alternative resources [69]. Cooper and Laing [20] stated that the application of crop residue for animal feeding and soil fertility maintenance is very important in maintaining balance and functionality in the rural system. Thus, crop residues play important roles for farmer’s livelihood, in various contexts and under different levels of resource availability [50]. In Ethiopia, and most other developing countries of Africa and Asia, crop residues and food wastes are used primarily for animal feeding [77]. In India, crop residues are enriched with urea and molasses as fodder for livestock [37]. In China, 31% of annual crop residue yield was applied to animal feeding [37, 70]. In Henan Province alone, Wang et al. [71] reported the application of 6.9 Mt of wheat straw, 6.0 Mt of corn stalk, and 2.2 Mt of peanut shell and leaves as forage in 2009 with a projected application of 4 Mt of agricultural residue to forage production in 2016. In Denmark, close to ½ of total collected crop residues are used for animal bedding and animal feed and fodder [1]. An estimated 3.6 Mt of dry crop residue was used for animal bedding in Canada in 2011 aside from the amount applied to supplement forage crops for animal feeding [1, 29]. Krausmann et al. [14] reported that of the 4.4 Tg yr−1 of crop residue, 2.9 Tg (66%) is appropriated for fodder, animal bedding, and energy. The authors reported that 10% of harvested residues were used to feed livestock in Europe and North America while 83% was used in South and Central Asia. Wirsenius et al. [78] reported global appropriation of 41% of total crop residue to food systems (i.e., livestock feeds) while Weiser et al. [79] reported that 24% of harvested cereal straw was used for livestock husbandry. In the EU, Scarlat et al. [80] reported that 1/5th to 1/3rd of harvested crop residues were applied to livestock production while Ericsson et al. [81] estimated 1/3rd. In SA, Batidzirai et al. [7] estimated that 260,000 tons yr−1 of maize stover out of the harvestable 9.7 Mt yr−1 was needed for cattle feed while 70,000 tons out of the harvestable 870,000 tons of wheat straw was applied to livestock bedding. In sub-Saharan Africa with predominantly small holder crop-livestock integration, crop residues are primarily applied to livestock production (fodder, feed, and bedding) such that allocation to other competing applications including soil conservation is problematic [50, 69, 74, 75].

3.3 Application of agro-industrial residues and food wastes in renewable energy production

Among the renewable sources of energy (hydropower, solar, geothermal, wave, wind, biomass, and tidal), only biomass can be converted to three different forms of energy carrier: solid, liquid, and gaseous biofuels [82]. The most common biofuels are bioethanol, biodiesel, and biogas. Bioethanol is generated from starch, sugar, and lignocellulosic-rich crops (phase I) and from food wastes and crop residues feedstocks (phase II); biodiesel is produced from oil rich crops, food wastes, and agricultural residue feedstocks; while biogas is produced from carbohydrate-rich biomass including animal wastes and manure [33]. Biofuels are used in different applications such as generation of electricity, heating, and powering of machines [33]. Generation of energy products from agricultural biomass has in addition environmental advantages: biomass source is storable, inexpensive, energy-efficient, and environmentally friendly. Biomass energy production and biofuel generation are major components of the circular and bioeconomic agro-industrial residue and food waste management option [52, 64, 65]. Utilization of agricultural residues and food wastes for large-scale modern bioenergy production is gaining attention in many countries [83, 84]. Countries such as Denmark, United Kingdom, Spain, Sweden, China, and India have developed large bioenergy facilities [85, 86]. Leading countries for bioethanol production are USA and Brazil [33]. Key residues are maize stover, wheat straw, rice straw and husks, and bagasse [21, 87, 88]. Bagasse is the most commonly used residue, but USA is pioneering the use of maize stover while Denmark is focusing on straw. A study by Bentsen et al. [16] estimated the theoretical global potential of primary agricultural residues from cereals and sugar cane available for biofuel production at approximately 3.7 billion tons of dry matter annually. Earlier studies [10, 14, 18] had estimated 2.7–3.5 billion tons yr−1. A more recent study by Panoutsou et al. [89] projected a technical potential of crop and agro-industrial residue availability for biofuel production in the EU28, Western Bulkans, Turkey, and Ukraine as 400,000 tons of dry biomass yr−1 by 2030. In Denmark, Gylling et al. [90] had projected an increase from 1.4 Mt yr−1 to approximately 3.0 Mt yr−1 by 2020. Studies by Larsen et al. [91] and Thomsen et al. [92] estimated that 50% of straw resources in Denmark are collected for various purposes, 45–50% of which is used for energy generation. Ericsson and Nilsson [81] and Scarlat et al. [80] reported that 20–40% of crop residues produced in Denmark was applied to energy generation. Annual straw consumption for domestic heat and power was put at approximately 1.4 Mt (fresh weight), and a significant proportion is channeled to biorefinery (biofuel, bioethanol), chemical, and material production [16, 80, 81]. It is projected that about 155 Mt of agricultural residue (including 60 Mt of manure) would be applied to bioenergy production in the United States by 2030 [11] without increasing the agriculture share of land resources [93, 94]. Regional estimates reported by UCS [11] include Texas (19.8 Mt), California (9.2 Mt), Alkansas (10.3 Mt), and Iowa (31 Mt). The “Billion ton annual supply study” [21] and its update [22] reported appropriation of 5.6 Mt (1% of total) of corn stover for energy production out of an annual crop residue production of 550 Mt [16]. US DOE [24] reported that 111 million dry tonnes (Mdt) and 94 Mdt of crop residue can be collected at farm-gate prices of $60 and $50, respectively; 3/4th of which are corn stover and 1/5th wheat straw. The study projected that by 2030, about 180 Mdt yr−1 residue will be available for biofuel production under the base-line scenario while about 320 Mdt yr−1 will be available under the high-yield scenario with 85% being corn stover. In addition are 20–26 Mdt of processing and other wastes at $40–$60 per dry ton (dt−1). Animal manure was estimated at 30–60 Mdt at farm-gate price of $50–$60 dt−1. IARI [37] reported that of the 700 Mt yr−1 of crop residues produced in China, 19% (~133 Mt) was used for energy generation while a theoretical estimate of 930.8 Mt of lignocellulosic biomass was reported for China by Ji [30]. The report also indicated that 13.5 Mt yr−1 of residues was theoretically available for biofuel production from 19 potential crops. Lignocellulosic biomass availability for bioenergy generation in Iran was reported to be about 11.33 Mt yr−1 by Alavijeh and Yaghmaei [31]. For SA, Batidzirai et al. [7] estimated the sustainable biomass energy potential to range from 400 to 550 PJ excluding energy crops, public grasslands, and roadside grasses. Components include maize and wheat residues (6 Mt yr−1 or 104 PJ energy equivalent, that is, 5.1 Mt yr−1 of maize stover at 94 PJ and 600,000 tons yr−1 of wheat straw at 10 PJ), forestry biomass residue (189 PJ: 1o = 41 PJ, 2o = 17 PJ, 3o = 70 PJ; wood chips = 61 PJ), sugar cane plantation and cane processing or bagasse (19–32 PJ), and organic waste from municipal solid wastes (4.5 Mt at 8 PJ). Barahira et al. [33] reported that 13.5 Mt of crop residues are potentially available for biofuel production in SA. In Nigeria and most other Sub-Saharan Africa, renewable energy production from agro-industrial and food wastes is still in its infancy, and large-scale industrial bioenergy production is yet to be accorded priority. Biomass conversion technologies currently applied at elemental level include physical or mechanical conversion (chipping, grinding, milling, and densification) into solid fuels such as briquette and pellets [39, 95, 96, 97]; thermochemical conversion (combustion, pyrolysis, gasification, and liquefaction) to produce biochar, bio-oil, and gas such as methane [39, 98, 99]; and biochemical conversion (anaerobic digestion, fermentation, and transesterification) to produce biogas, ethanol, and biodiesel [100, 101, 102]. Jakayinfa et al. [39] estimated the theoretical bioenergy potential of agricultural residues and animal wastes for Nigeria at 5.81 EJ (3.64 EJ from agricultural residues and 2.17 EJ from animal wastes) while the technical potential, based on generalized availability factor of 0.3 [103] (range: 0.0–1.0 depending on type of crop residue), was estimated at 1.74 EJ. For Tanzania, total bioenergy potential of crop residues was put at 5714.0 TJ in 2012 with sugarcane and cassava having the highest potential of 2966.4 and 845.0 TJ yr−1, respectively, while a total of 1397.0 TJ yr−1 could be generated from animal waste with cattle having the highest potential of 1,139,074,332 MJ yr−1 followed by goat (181,036,476 MJ yr−1). The least bioenergy potential was for poultry manure (7,859 MJ yr−1) [6].

3.4 Agro-industrial wastes as substrates for edible fungi (mushroom) cultivation

A rapidly expanding valorization of agro-industrial residues is as substrates for edible fungi (mushroom) cultivation (Figure 6). Mushroom cultivation is seen as a major and sustainable component of modern agricultural residue management protocol and circular agricultural systems [105, 106]. Data on global or country-specific allocation of crop residues to mushroom production are scarce in literature. IEA [1] reported that in Canada, about 1.0 Mdt of crop residues were applied to mushroom and horticultural cultivation in 2011. In China, Wang et al. [71] reported that application of agricultural residues to mushroom production has been commercialized. Total crop residue applied to mushroom cultivation in Henan province in 2009 was 2.44 Mt, which accounts for 3% of crop residue generation and 4% of total crop residue utilization in the province. Of these volumes, wheat straw accounted for 0.68 Mt, rice straw, 0.53 Mt [72]. In Luoyang alone, 52 ha and about 200,000 tons of residues were dedicated to mushroom cultivation annually [71, 72]. In India, Raman et al. [107] reported that a total of 39 kinds of agricultural residues from 26 crops provide valuable resources for mushroom cultivation. According to the report, India produces over 620 Mt yr−1 of agricultural residue, a substantial quantity of which could be profitably channeled to mushroom production. In eastern Democratic Republic of Congo, Kaziga et al. [108] reported favorable results of an effort to orientate smallholder farmers to valorize wastes from stable crops through mushroom production.

Figure 6.

Major edible mushrooms on agricultural residue substrates [104].

Global mushroom production has increased tremendously over the past decades from about 0.35 Mt in 1965 to about 3.41 Mt in 2007 [107, 109, 110, 111]. In 2015, global mushroom market was worth USD 35 billion [107] while Royse et al. [104] reported that global mushroom market was worth USD 63 billion in 2013 made up of medicinal mushrooms: 38%, wild mushrooms: 8%, and edible mushrooms: 54%; with an annual projected increase by USD 34–60 billion [105]. In addition to contributing to food and nutrition security, spent mushroom substrate (SMS) represents a vital resource to produce high-quality compost for growth of other fungi [112], improve animal nutrition and health [105, 106, 113, 114], produce materials [115, 116, 117], and extract enzymes for industries [105, 106, 109] and for soil amendment and bioremediation [106, 114, 118, 119]. China is the global leader in mushroom production with 3,918,300 tons yr−1 or 64% of global volume and 85% for oyster mushroom production (Pleurotus spp.) [109, 110].

3.5 Derivation of bioactive molecules from agro-industrial residues and food wastes

Agricultural residue and food waste biomass stream are widely acclaimed as valuable resources for bioactive compounds (molecules) and functional products. Valorization of agro-industrial residues into food and feed ingredients, dietary supplements, novel bio-components, nutraceuticals, and pharmaceuticals is a potential huge industry and a vital component of the bio-economic and circular model of agricultural residue management. Bioactive molecules from agricultural and food residues include phenols, polyphenols, non-starch polysaccharides (cellulose, hemi-cellulose, and lignin), oligosaccharides, carotenoids, soluble fibers, terpenoids, proteins, tocopherols, and phytosterols [47, 48, 120, 121]. Animal wastes and residues (dairy waste, sea food waste, slaughter wastes) have high levels of proteins, lipids, and minerals [48, 122, 123]. Prado et al. [124] had observed that animal and vegetable wastes are low-cost materials for bioactive compounds using suitable processes. The extraction of bioactive compounds can be integrated into bioenergy facilities, thus enhancing revenue potentials [67, 125]. These bioactive molecules or metabolites can impact human and animal health, for instance, as antioxidant, immunomodulatory, anti-hypertensive, anti-inflammatory, cholesterol reducing, antiaging, anti-cancer, and antidiabetic agents [48, 126, 127, 128]; as well as serve as raw materials for the development of functional ingredients useful in food, cosmetics, chemical, and pharmaceutical industries [48, 67, 129, 130, 131, 132]. Figure 7 shows the main classes of bioactive compounds that are derivable from agro-industrial and food waste biomass.

Figure 7.

The main classes of bioactive compounds [133].

Traditional and novel approaches for extraction of bioactive molecules from organic agricultural and food wastes (Figure 8) include (a)solvent extraction (characterized by low processing cost and ease of operation) [120], (b) microbial fermentation (solid-state fermentation) [48, 70, 134, 135, 136, 137], (c) supercritical fluid extraction (SFE) [13, 120, 138, 139], (d) subcritical water extraction (SCWE) (characterized by shorter extraction time, lower solvent cost, high quality product, and eco-compatibility) [13, 120, 138, 140, 141], (e) enzyme assisted extraction (EAE) (uses water as solvent, and employs enzymes such as α-amylase, proteases, chitinase, tanase, cellulase, β-glucosidase, xylanase, β-glucanase, and pectinase, which help to degrade cell wall structure and depolymerize plant cell wall polysaccharides, facilitating the release of linked compounds) [13, 48, 120, 142, 143, 144], (f) ultra-sound assisted extraction (UAE) [13, 120, 134, 138, 145, 146, 147], pulse electric field-assisted extraction [13], and (g) micro-wave assisted extraction (MAE) (characterized by shorter extraction time, higher extraction rate, lesser solvent requirement, and lower cost) [13, 120, 134, 147, 148, 149]. Generally, the choice of applied extraction method and recovery rate depends on residue or waste type and bioactive compound of interest [13, 150, 151]. To enhance the efficiency of conventional extraction methods, deep eutectic solvents (DESs) and natural deep eutectic solvents (NADESs) have been suggested to replace organic solvents for extraction of bioactive compounds from agricultural waste biomass materials [13, 152, 153]. Also, the application of encapsulation and nanoemulsion to enhance the stability, bioavailability, and accessibility of derived bioactive compounds is being studied [13, 154, 155].

Figure 8.

A schematic representation of different techniques for extraction of bioactive compounds from food wastes and their health benefits [120].

Khaksar et al. [47] suggested the integration of metabolomics approaches into extraction of bioactive compounds from organic agricultural wastes to gain deeper understanding of the metabolic profile of agro-industrial wastes and enhance their value. Metabolomics approaches include liquid chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), nuclear magnetic resonance spectroscopy (NMR), and high-performance liquid chromatography (HPLC). Metabolomics had enabled the discovery of over 10,000 different phenolic structures with diverse natures including phenolic acids, flavonoids, and tannins [47, 156].

3.6 Agro-industrial residues as resources for production of materials

Agricultural residues can also be valorized as substrates for production of insects as sources of fat and proteins [67]. Arthropods such as flies and maggots can grow on a variety of organic matter including animal manure, vegetable, and fruit wastes. These arthropods can be converted to animal flour of higher protein content and incorporated as sources of protein and fat in animal feed (livestock, aquaculture, pet) [67]. Larval digestion (bioconversion or biotransformation) of plant and animal materials yield high-value products such as organic fertilizers [67]. In addition, high-value products such as chitin, antibiotics, and peptides with bio-stimulant activity can be extracted for use in animal health and nutrition [67]. Other useful biocompounds derivable from agricultural residues include biopesticides [157, 158], pectin as edible food coating [159, 160], natural aromas [67, 161], quercetin, and flavonols [67, 162]. The replacement of non-recyclable raw materials for production of functional components in industries has become essential as a waste management strategy and in line with circular economic principles. Consequently, valorization of agricultural waste biomass and food wastes to functional materials is being promoted. Growth or culture media, packaging materials, biochar, biopolymers, bioplastics, single cell proteins (from microbial biomass), enzymes, organic acids, biofertilizers, and compost are materials derivable from agricultural residues [13, 67, 134, 163, 164, 165, 166, 167]. Biopolymers and bioplastics are highly biodegradable, biofunctional, biostable, and biocompatible and have wide applications in cosmetics, pharmaceutical, chemical, food, and beverage industries [13, 168].

3.7 Valorization of agro-industrial residues through activated charcoal production

Activated biochar or activated carbon or activated charcoal (AC) is a carbonaceous material of high surface area, and large pore volume, widely employed for adsorption of pollutants such as toxins, poisons, metals, and chemicals. Activated carbon production from agricultural residues and food wastes is viewed as a major valorization product with considerable and sustainable potential for application in various fields including bioremediation, water treatment, soil amendment, soil fertility, enhancement of soil biophysical and chemical characteristics, carbon sequestration, medical health, animal health, animal production, horticulture, and climate change mitigation [52, 169, 170]. Biochar production from agro-industrial and food wastes is particularly important in developing countries including Nigeria owing to its simplicity and wide applications. Adding activated carbon to soils could lock away carbon for centuries owing to slow microbial decomposition [171, 172, 173]. Minasny et al. [174] submitted that recycling stable crop residues as biochar substantially contribute to carbon sequestration in soils. Biochar addition to soil was shown to increase crop yield by about 25% on average [172, 175] attributed to enhanced cation exchange capacity, soil aggregation, and hydraulic conductivity [176]. In industrial waste water treatment, AC is widely employed for reduction of pollutants such as heavy metals and toxic chemicals (e.g., phenols and their derivatives) [177]. The surface chemistry of activated charcoal confers on it the ability to adsorb many gases, aqueous liquid, chemicals, and poisons [177, 178, 179]. Several studies showed that activated charcoal is harmless even when it is accidentally consumed, inhaled, or comes in contact with the skin. When mixed with water and swallowed to counteract poisoning, activated charcoal adsorbs the poison or drug, inactivating it and then carries it inert through the entire length of the digestive tract out of the body [180]. Majewska [181] reported a 3.5–5.0% increase in body weight and higher carcass and organ weights compared with control in broiler chickens on 3% dietary inclusion level of hard wood charcoal. The author attributed the results to the detoxifying effects of charcoal, lowered surface tension of the intestinal digesta, and enhanced liver function with respect to fat digestion. Jiya [182] supplemented activated charcoal at 0.5% in broiler feeds and noted increased relative organ weights and reduced cholesterol level in the carcass attributed to efficient mineral uptake and nutrient utilization. Drunna et al. [183] reported improved growth rate and reduced flatulence, fly population, and litter odor at varied inclusion levels of wood charcoal in feed of broiler chickens. Dim et al. [184] observed improved daily weight gain and feed conversion ratio in broiler chickens fed 6% dietary charcoal inclusion compared with other groups. Linhoss et al. [185] reported positive effects of biochar in litter amendment in broiler production while Schmidt et al. [186] reported that biochar has the potential to improve animal health, feed efficiency, and livestock housing climate; reduce nutrient losses and greenhouse gas emissions; increase soil organic matter content, and thus soil fertility. Zhang et al. [187] observed that biochar remediates organic pollutants by hydrogen binding, surface complexation, electrostatic attractions, and acid-base interactions; and heavy metals in soils by precipitation, surface complexation, chemical reduction, cation exchange, and electrostatic attraction. Biochar can improve cation exchange capacity, neutralize acidic soils, and enhance soil fertility [134, 188, 189]. It enhances organic solid waste decomposition by enhancing microbial population. It removes pollutants such as antibacterial drugs from water and wastewater [190, 191].

Traditionally, AC was produced from coal, lignite, petroleum residue, and hard wood biomass (fossil-related resources) [177, 178]. These materials are costly, exhaustible, and unfriendly to the ecosystem [177, 192]. Today, recyclable agro-industrial residues and food wastes are promoted as viable and sustainable alternatives being renewable, readily available, inexpensive, environmentally friendly, and an additional income to growers, farmers, and vendors [67, 177, 193]. Generally, the use of agricultural wastes such as corn cob, groundnut shell, poultry litter, rice husk, palm kernel shell, and coconut shell in the production of value-added products is gaining momentum [67, 173, 178, 194]. Activated carbon can hence be produced from all plant parts, animal manure, bones, fruit and tuber peels, husks, corn cob, stalk, straw, shell, and fruit stone [52, 67, 178]. These materials are broadly classified as woody materials composed of cellulose, hemicellulose, and lignin, and non-woody biomass composed of cellulose, hemicellulose, lignin, lipids, proteins, sugars, water, hydrocarbons, starch, and many other functional groups such as carbonyl, carboxylic, chromene, ethers, lactone, phenol, pyrone, and quinone groups, which contribute to the physicochemical properties and activity of the final product [178, 195]. Generally, choice of feedstock for AC production is informed by high carbon content, low inorganic matter, high density, and high content of volatile matter, ready availability, and low cost, low rate of degradation during storage, and high AC yield upon pyrolysis [173, 178, 195]. Studies on AC production from bioresources include tomato waste [196], corn cob [197], corn stalk [198], groundnut shell [199], palm kernel shell [200, 201], coconut shell [202, 203], chestnut oak shell [204], peanut shell [147, 205, 206, 207, 208], rice husk and straw [209, 210], apple waste [211], grape stalk [212], coffee grounds [213], palm oil mill residue [214, 215], oil palm empty fruit bunch [216, 217], bio-waste mixtures [218], food waste [177], poultry litter [203, 219, 220], pig dung [203, 221], dairy cattle carcass [222], cow dung [203, 223], and chicken feather [224].

The characteristics, properties, and performance of any AC sample would depend on the type of feedstock, temperature, and resident time of pyrolysis (carbonization) [134, 177, 178, 218], the activation process adopted: physical, chemical, or physicochemical [177, 218, 225], as well as the content of inorganic elements and other functional groups [177, 218]. These factors influence the internal pore structure of the AC, which determines its adsorbent capacity [177, 218]. Pores are classified as micropores (< 2nm), mesopores (2–50 nm), and macropores (> 50 nm) [177, 218, 226]. Figure 9 is a schematic representation of pore structure in activated carbon. The higher the internal pore structure, the more the surface area and adsorbent capacity of the AC [177, 178].

Figure 9.

Pore structures in activated carbon (AC) [227].

3.7.1 Production process of activated carbon

In principle, AC production involves physical or chemical treatment [178]. Physical treatment includes carbonization of feedstock in the absence of oxygen and in the presence of an inert gas (e.g., argon, Ar) followed by activation of the charcoal (biochar or carbon) using an oxidizing agent (steam, CO2, or their mixture). Chemical treatment involves carbonization of feedstock to which had been added an activating agent (a strong dehydrating and oxidizing agent such as H3PO4, ZnCl2, KOH, NaOH, and H2SO4 under nitrogen atmosphere. Thus, two principal steps: carbonization and activation, are involved in AC production [177, 178, 218, 228]. Equipment for AC production varies in sophistication depending on the degree of mechanization.

Carbonization aims to decompose the feedstock, eliminate non-carbon species (volatile matter, non-carbon elements, namely nitrogen, oxygen, hydrogen, sulfur; aromatics, etc.) and deposit biochar (charcoal or carbon) having essentially a fixed carbon content [178] and substantial pore structure. Reported pyrolysis (carbonization) temperature and resident time vary widely probably on account of differences in feedstock material, level of sophistication of equipment and automation, as well as other environmental conditions. Generally recommended temperature range is 400–900°C under inert atmosphere [75, 229, 230]. Budi et al. [231], however, reported pyrolysis of coconut shell in a kiln at 75–150°C for 6 h in argon atmosphere. Yasin and Pravinkumar [218] pyrolyzed wood pieces at 400–500°C, coconut shell at 320–400°C, and saw dust at 200–300°C. Yu et al. [177] using a vertical tube furnace pyrolyzed a blend of food wastes at 275–525°C for 30–120 min.

Activation is a key step in AC production, which aims to enhance the critical performance parameters of AC such as pore structure, pore volume, porosity, surface area, fixed carbon, and mineral contents. Activation can be by physical or chemical treatments. Physical activation involves treating biochar with an oxidizing gas or a combination of oxidizing gases such as oxygen, carbondioxide, and steam at high temperatures commonly in the range 500–1000°C [178]. Budi et al. [228] reported physical activation of biochar derived from coconut shell in argon gas furnace at 532, 700, and 868°C for 10–120 min. The activating gas opens previously formed pores blocked by tar or pyroligneous liquids formed during carbonization, creates new pores, and widens existing ones by removal of reactive carbon species, and other volatile contents of the biochar [177, 178]. The reaction(s) during physical activation could involve the below [178]:

In chemical activation, strong dehydrating and oxidizing chemicals are employed. These include alkali: potassium hydroxide (KOH) [177, 178], potassium carbonate (K2CO3) [153, 177, 178, 232], sodium hydroxide (NaOH) [177, 178, 233], and sodium carbonate (Na2CO3) [178]; alkali earth metal: aluminum chloride (AlCl3) [178], and zinc chloride (ZnCl2) [177, 178, 230, 231, 233, 234, 235, 236, 237, 238, 239]; and acid: phosphoric acid (H3PO4) [177, 178, 218], and sulfuric acid (H2SO4) [177, 178, 236]. The raw material for biochar production is usually impregnated with the appropriate activating agent prior to carbonization (pyrolysis). The activating agent acts as a dehydrating and/or oxidizing agent, promotes decomposition of the feedstock, inhibits deposition of tar and volatile contents [218] such as pyroligneous liquids, and enhances activated charcoal yield, carbon content, porosity, and surface area. At the end of the process, the resulting activated carbon is washed in acid or alkali depending on the activating agent used in order to remove remaining activating agent lodged in the pore structure [218]. An alternative procedure is to immerse biochar resulting from pyrolysis in the choice activating agent for a time duration of 24 h [231] followed by washing and drying. Esmar Budi et al, [231] reported the application of double activation, which involved chemical activation followed by physical activation using a horizontal furnace at 400°C in argon (Ar) gas (200 kg m−3) environment for I h. Whereas activated charcoal produced by physical activation is neater and requires no further washing that from chemical activation has higher surface area and pore volume. Chemical activation also requires lower temperature commonly of range 450–600°C [177]. Among the chemical activators, ZnCl2 and H3PO4 are the most applied in the industry [177]. The atmosphere for chemical activation is either inert gas (e.g., Ar) or air [177].

A number of studies have evaluated the physicochemical properties of AC derived from a wide range of recyclable biological waste materials under varied pyrolysis conditions, activation agents, and time duration. Budi et al. [228] studied the effect of activation temperature (532, 700, and 868°C), and resident activation time (10, 60, and 120 min) under argon gas pressure (6.59, 15, and 23.4 kg/cm2) on pore structure and carbon content of coconut-shell-derived biochar and reported decreases in pore size but increases in pore volume and uniform pore distribution with increasing activation temperature, resident activation time, and gas pressure. Resident activation time alone did not influence pore size and pore distribution. The authors attributed the increase in pore volume to formation of new pores especially micro pores due to release of more volatile components from the biochar, as well as decreased pore size. Increase in pore volume increases the surface area of the activated carbon sample. The authors also reported increase in carbon content, which was attributed to the increase in pore numbers with increase in activation temperature, which caused the release of more volatile components. Esmar Budi et al, [231] evaluated the effects of chemical and physical activation on coconut-shell-derived charcoal. Chemical activation was performed with KOH (30, 40, 50, and 60%), NaOH (1, 2, 4, 7, and 11%), HCl (2, 4, and 6%), and H3PO4 (2, 4, and 6%) for 24 h while physical activation was with steam at 400°C in argon gas environment (200 kg m−3) for 1 h. There were increases in pore size; pore number initially increased but decreased as chemical concentration increased. Carbon content decreased with increasing chemical concentration. The decrease in pore number was linked to excessive widening of pre-formed pores, coalesce of pores, and collapse of carbon structure due to excessive chemical attack. The authors also noted an increase in total surface area, which was attributed to formation of new micro pores, and widening of existing pores. Yasin and Pravinkumar [218] investigated the effects of pyrolysis parameters and chemical (phosphoric acid, H3PO4) activation on properties of charcoal derived from some bio-waste materials. Biochar yield was higher with increasing pyrolysis temperature and resident time, and yield varied with type of starting material with coconut shell (56.66–63.33%) > saw dust (50.00–56.66%) > wood piece (46.66–53.33%%) at all temperatures and time duration. The result was attributed to higher loss of volatile components in the feedstock and higher oxidization of reactive carbon species at the optimal pyrolysis temperature and time duration. Activated charcoal adsorbent capacity was positively correlated with activation temperature and biochar from coconut shell had higher values than that from other materials (1.95–2.67 vs 1.73–1.97 vs 1.45–1.92 mg g−1 for coconut shell vs saw dust vs wood piece). Bulk density did not vary clearly with activation temperature, but values were highest for wood piece (0.75–0.78 gm/cm3) compared with coconut shell (0.56–0.58 gm/cm3) and saw dust (0.18–0.21 gm/cm3). Moisture content followed a similar trend as bulk density being highest in wood piece (4.35–5.25%) compared with coconut shell (2.21–3.10%) and saw dust (1.07–1.25%). Volatile matter was highest in saw-dust-activated charcoal (12.60–18.10%) compared with wood piece and coconut shell (11.25–12.35 and 7.30–7.40%, respectively) while ash content was highest in biochar from wood piece (6.95–7.85%) compared with saw dust (5.95–6.15%) and coconut shell biochar (1.50–1.75%). Biochar from coconut shell had the highest content of fixed carbon (88.10–88.88%) compared with saw dust (74.53–80.18%) and wood piece (74.55–77.45%).High bulk density, moisture, and volatile matter are undesirable properties of activated charcoal. A good activated carbon should be highly porous (high total pore volume), of high fixed carbon content and surface area, which enables high adsorption capacity [177]. In a study that evaluated the physicochemical properties and adsorption capacity of biochar and physically (steam) activated biochar derived from a complex of edible food waste feedstock, Yu et al. [177] observed increased biochar yield with increasing pyrolysis temperature and longer pyrolysis resident time. Carbon content also increased with pyrolysis temperature, but this became stable after 60 min pyrolysis duration. Activated carbon yield reduced with higher activation temperature and longer activation time. Before activation, biochar surface area was 10 m2 g−1, micro pore volume was 0.004 cm3 g−1, and total pore volume was 0.016 cm3 g−1. These indices ranged between 288 and 745 m2 g−1, 0.072 and 0.196 cm3 g−1, and 0.160 and 0.792 cm3 g−1, respectively, after activation. The activation temperature and time duration for the highest activated carbon surface area (745 m2 g−1), micro pore volume (0.196 cm3 g−1), and total pore volume (0.792 cm3 g−1) were 950°C and 1 h, 850°C and 3h, and 950°C and 5 h, respectively. Thus, surface area and total pore volume increased with activation temperature while micro pore volume reached maximum value at 850°C. Biochar and activated carbon produced at 750°C had very small volume of meso and macro pores but higher activation temperatures (850 and 950°C) produced enlarged pores yielding more meso and macro pores. Longer activation time reduced surface area and micro pore volume but increased total pore volume at 950°C. Larger pores were obtained with increased activation time, thereby reducing number of micro pores. Because larger pores have relatively smaller surface area, converting micro pores to meso and macro pores will reduce activated carbon surface area. The authors reported that carbon content was 48.8% in the feedstock, 71.9% in derived biochar (pyrolysis temperature, 525°C for 2 h), and 68.8% after activation at 750°C for 3 h, 62.6% at 850°C for 3 h, 40.9% at 950°C for 3 h, 48.0% at 950°C for 1 h, and 33.2% at 950 for 5 h clearly showing reduced fixed carbon with increasing activation temperature and activation duration. Nitrogen (N), H, and S content followed a similar trend as fixed carbon. Sodium (Na), Ca, and P increased with activation temperature and time duration and were generally higher in activated sample than in biochar and feedstock. It does appear, hence, that increased activation temperature and time duration preserved the mineral content of biochar.

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4. Conclusion and future perspective

With rising global human and animal population, demand for food, and food production will continue to increase leading to increases in waste generation and negative environmental challenges. Sustainable agricultural production and agro-industrial processing, environmental, human, animal, and climate health depend substantially on effective waste management. Circular agricultural production and bioeconomic agro-industrial waste management models are key to achieving the vision to considerably reduce waste generation, reuse wastes, and recycle wastes. Continued intellectual brainstorming and research will enable the arrival at the goal of turning wastes to wealth and an agricultural production system that produces nil wastes.

References

  1. 1. IEA (International Energy Agency). Mobilization of agricultural residues for bioenergy and higher value bio-products: Resources, barriers and sustainability. IEA Bioenergy Task. 2017;43:1
  2. 2. Torén J, Wirsenius S, Anttila P, Böttcher H, Dees M, Ermert J, et al. Biomass Energy Europe: Executive Summary, Evaluation and Recommendations. Freiburg: University of Freiburg; 2011
  3. 3. Sadh PK, Duhan S, Duhan JS. Agro-industrial waste and their utilization using solid state fermentation: A review. Bioresources and Bioprocessing. 2018;5:1
  4. 4. Mendu V, Shearin T, Campbell JE Jr, Stork J, Jae J, Crocker M, et al. Global bioenergy potential from high-lignin agriculture residue. PNAS. 2012;109(10):4014-4019. DOI: 10.1073/pnas.1112757109
  5. 5. Biomass Energy Europe. Status of biomass resource assessmentsversion 3. 2010
  6. 6. Lyakurwa FS. Assessment of the energy potential of crop residues and animal waste in Tanzania. Independent Journal of Management and Production. 2016;7(4):1227-1239
  7. 7. Batidzirai B, Valk M, Wicke B, Junginger M, Oaioglu V, Euler W, et al. Current and future technical, economic and environmental feasibility of maize and wheat residue supply for biomass energy application: Illustrated for South Africa. Biomass and Bioenergy. 2016;92:106-129
  8. 8. Kemausuor F, Kamp A, Thomsen ST, Bensah EC, Østergård H. Assessment of biomass residue availability and bioenergy yields in Ghana. Resources, Conservation and Recycling. 2014;86:26-37
  9. 9. Belewu MA, Babalola FT. Nutrient enrichment of some waste agricultural residues after solid state fermentation using Rhizopusoligosporus. Journal of Applied Bioscience. 2009;13:695-699
  10. 10. Lal R. World crop residues production and implications of its use as a biofuel. Environment International. 2005;31(4):575-584
  11. 11. UCS (Union of Concerned Scientists). Turning Agricultural Residues and Manure into Bioenergy. Cambridge: UCS; 2014
  12. 12. Cho EJ, Trinh LTP, Song Y, et al. Bioconversion of biomass waste into high value chemicals. Bioresource Technology. 2020;298:122386. DOI: 10.1016/j.biortech.2019.122386
  13. 13. Capanoglu E, Nemli E, Tomas-Barberan F. Novel approaches in the valorization of agricultural wastes and their applications. Journal of Agricultural and Food Chemistry. 2022;70(23):6787-6804. DOI: 10.1021/acs.jatc.1co7104
  14. 14. Krausmann F, Erb K-H, Gingrich S, Lauk C, Haberl H. Global patterns of socioeconomic biomass flows in the year 2000: A comprehensive assessment of supply, consumption and constraints. Ecological Economics. 2008;65:471
  15. 15. Rogner H-H, Aguilera RF, Bertani R, Bhattacharya SC, Dusseault MB, Gagnon L, et al. Chapter 7 - Energy Resources and Potentials. Global Energy Assessment - Toward a Sustainable Future. Cambridge, UK: Cambridge University Press; 2012. pp. 423-512
  16. 16. Bentsen NS, Felby C, Thorsen BJ. Agricultural residue production and potentials for energy and material services. Progress in Energy and Combustion Science. 2014;40:59-73
  17. 17. Smil V. Crop residues: Agriculture’s largest harvest - crop residues incorporatemore than half of the world agricultural phytomass. Bioscience. 1999;49:299
  18. 18. Hakala K, Kontturi M, Pahkala K. Field biomass as global energy source. Agricultural and Food Science. 2009;18:347
  19. 19. Food and Agricultural Organization. FAOStats 2001. Rome: FAO; 2001
  20. 20. Cooper CJ, Laing CA. A macro analysis of crop residue and animal waste as a potential energy source in Africa. Journal of Energy in Southern Africa. 2007;18(1):10-19. DOI: 10.17159/2413-3051/2007/v 18i/93339
  21. 21. Perlack RD, Wright LL, Turnhollow AF, Graham RL, Stokes BJ, Erbach DC. Biomass as Feedstock for a Bioenergy and Bioproducts Industry: The Technical Feasibility of a Billion-ton Annual Supply. Oak Ridge TN: Oak Ridge National Laboratory; 2005
  22. 22. U.S. Department of Energy. U.S. billion-ton Update: Biomass Supply for a Bioenergy and Bioproducts Industry. Oak Ridge National Laboratory: Oak Ridge, TN, USA; 2011. p. 227
  23. 23. Chatterjee A. Annual crop residue production and nutrient replacement costs for bioenergy feedstock production in United States. Agronomy Journal. 2013;105:685
  24. 24. U.S. DOE. 2016 Billion-Ton Report: Advancing Domestic Resources for a Thriving Bioeconomy. Oak Ridge, TN, USA: Oak Ridge National Laboratory; 2016
  25. 25. Kim S, Dale BE. Global potential bioethanol production from wasted crops and crop residues. Biomass and Bioenergy. 2004;26(4):361-375
  26. 26. Bloomberg. Biomass Supply Costs – Fields of Gold? London: UK, Bloomberg New Energy Finance; 2011
  27. 27. de Wit M, Faaij A. European biomass resource potential and costs. Biomass and Bioenergy. 2010;34(2):188-202
  28. 28. Energinet.dk. Energikoncept 2030 - Baggrundsrapport [Energy concept 2030 - Background report]. Fredericia, DK, Energinet.dk. 2015
  29. 29. Li X, Mupondwa E, Panigrahi S, Tabil L, Sokhansanj S, Stumborg M. A review of agricultural crop residue supply in Canada for cellulosic ethanol production. Renewable and Sustainable Energy Reviews. 2012;16(5):2954-2965
  30. 30. Ji L-Q. An assessment of agricultural residue resources for liquid biofuel production in China. Renewable and Sustainable Energy Reviews. 2015;44:561-575
  31. 31. Alavijeh MK, Yaghmaei S. Biochemical production of bioenergy from agricultural crops and residue in Iran. Waste Management. 2016;52:375-394
  32. 32. Pradhan A, Mbohwa C. Development of biofuels in South Africa: Challenges and opportunities. Renewable and Sustainable Energy Reviews. 2014;39:1089-1100
  33. 33. Barahira DS, Okudoh VI, Eloka-Eboka AC. Suitability of crop residues as feedstock for biofuel production in South Africa: A sustainablewin-win scenario. Journal of Oleo Science. 2021;2021:1-14. DOI: 10.5650/jos.ess20288
  34. 34. Devi S, Gupta C, Jat SL, Parmar MS. Crop residue recycling for economic and environmental sustainability: The case of India. Open Agriculture. 2017;2:486-494. DOI: 10.1515/opag-2017-0053
  35. 35. GoI. Annual Report 2016. New Delhi: Ministry of New and Renewable Energy; 2016
  36. 36. Pathak BS. Crop Residue to Energy. In: Chadha KL, Swaminathan MS, editors. Environment and Agriculture. New Delhi: Malhotra Publishing House; 2004. pp. 854-869
  37. 37. IARI. Crop Residue Management with Conservation Agriculture: Potential, Constraints and Policy Needs. New Delhi: Indian Agricultural Research Institute; 2012. p. 32
  38. 38. FAO. Crop Residue and Agro-industrial By-products in West Africa: Situation and Way Forward for Livestock Production. Rome: Food and Agriculture Organization; 2014
  39. 39. Jekayinfa SO, Orisaleye JI, Pecenka R. An assessment of potential resources for biomass energy in Nigeria. Resources. 2020;9:92-132. DOI: 10.3390/resources9080092
  40. 40. Ben-Iwo J, Manovic V, Longhurst P. Biomass resources and biofuels potential for the production of transportation fuels in Nigeria. Renewable and Sustainable Energy Reviews. 2016;63:172-192. DOI: 10.1016/j.rser.2016.05.050
  41. 41. Agba MM, Ushie EF, Abam I, Agba MS, Okoro J. Developing the biofuel industry for effective rural transportation. European Journal of Scientific Research. 2010;40:441-449
  42. 42. Simonyan K, Fasina O. Biomass resources and bioenergy potentials in Nigeria. African Journal of Agriculture. 2013;8:4975-4989. DOI: 10.5897/AJAR2013.6726
  43. 43. Ishola MM, Brandberg T, Sanni SA, Taherzadeh MJ. Biofuels in Nigeria: a critical and strategic evaluation. Renewable Energy. 2013;55:554-560. DOI: doi.org/10.1016/j.renene.2012.12.021
  44. 44. Okeh OC, Onwosi CO, Odibo FJC. Biogas production from rice husks generated from various rice mills in Ebonyi State, Nigeria. Renewable Energy. 2014;62:2048
  45. 45. Akorode MF, Ibrahim O, Amuda SA, Otuoze AO, Olufeagba BJ. Current status and outlook of renewable energy development in Nigeria. Nigerian Journal of Technology. 2017;36(6):196-212
  46. 46. Harris DR, Hillman GC. Foraging and Farming: The Evolution of Plant Exploitation. London, UK: Routledge; 2014
  47. 47. Khaksar G, Sirijan M, Suntichaikamolkul N, Sirikantaramas S. Metabolomics for agricultural waste valorization: Shifting toward a sustainable bioeconomy. Frontiers in Plant Science. 2022;13:938480. DOI: 10.3389/fpls.2022.938480
  48. 48. Lemes AC, Egea MB, de Oliveira Filho JG, Gauterio GV, Ribeiro BD, Coelho MAZ. Biological approaches for extraction of bioactive compounds from agro-industrial byproducts: A review. Frontiers in Bioengineering and Biotechnology. 2022;9:802543. DOI: 10.3389/fbioe
  49. 49. Dini I, Izzo L, Graziani G, Ritieni A. The nutraceutical properties of Pizza napoletana marinara TSG a traditional food rich in bioaccessible antioxidants. Antioxidants. 2021;10:495
  50. 50. Valbuena D, Tui SH-K, Erenstein O, Teufel N, Duncan A, Abdoulaye T, et al. Identifying determinants, pressures and trade-offs of crop residue use in mixed smallholder farms in Sub-Saharan Africa and South Asia. Agricultural Systems. 2015;134:107-118
  51. 51. Lohan S, Jat H, Yadav A, Sidhu H, Jat M, Choudhary M, et al. Burning issues of paddy residue management in north-west states of India. Renewable and Sustainable Energy Reviews. 2018;81:693-706
  52. 52. Venkatramanan V, Shah S, Rai AK, Prasad R. Nexus between crop residue burning, bioeconomy and sustainable development goals over North-Western India. Frontier in Energy Research. 2021;8:614212. DOI: 10.3389/fenrg.2020.614212
  53. 53. Lopes AA, Viriyavipart A, Tasneem D. The role of social influence in crop residue management: Evidence from Northern India. Ecological Economics. 2020;169:106563
  54. 54. Ravindra K, Singh T, Mor S. Emissions of air pollutants from primary crop residue burning in India and their mitigation strategies for cleaner emissions. Journal of Cleaner Production. 2019;208:261-273. DOI: 10.1016/j.jclepro.2018.10.031
  55. 55. Chawala P, Sandhu HAS. Stubble burn area estimation and its impact on ambient air quality of Patiala & Ludhiana district, Punjab, India. Heliyon. 2020;6:e03095. DOI: 10.1016/j.heliyon.2019.e03095
  56. 56. Jat HS, Jat RD, Nanwal RK, Lohan SK, Yadav AK, Poonia T, et al. Energy use efficiency of crop residue management for sustainable energy and agriculture conservation in NW India. Renewable Energy. 2020;155:1372-1382. DOI: 10.1016/j.renene.2020.04.046
  57. 57. Jethva H, Torres O, Field R, Lyapustin A, Gautam R, Kayetha V. Connecting crop productivity, residue fires, and air quality over northern India. Scientific Reports. 2019;9:16594. DOI: 10.1038/s41598-019-52799-x
  58. 58. Li R, Chen W, Zhao H, Wu X, Zhang M, Tong DQ , et al. Inventory of atmospheric pollutant emissions from burning of crop residues in China based on satellite-retrieved farmland data. China Geographical Science. 2020;30:266-278
  59. 59. Sarkar S, Singh RP, Chauhan A. Increasing health threat to greater parts of India due to crop residue burning. The Lancet Planetary Health. 2018;2:e327-e328. DOI: 10.1016/S2542-5196(18)30166-9
  60. 60. Sokhansanj S, Yadav YK, Lau A, Yadvika ME, Verma K. Identification of techno-economic viable crop residue utilization in India. Journal of Sustainable Bioenergy Systems. 2021;11:94-104. DOI: 10.4236/jsbs.2021.112007
  61. 61. Chakrabarti S, Khan M, Kishore A, Roy D, Scott S. Risk of acute respiratory infection from crop burning in India: Estimating disease burden and economic welfare from satellite and national health survey data for 250 000 persons. International Journal of Epidemiology. 2019;48:1113-1124. DOI: 10.1093/ije/dyz022
  62. 62. Sarkar S, Skalicky M, Hossain A, Brestic M, Saha S, Garai S, et al. Management of crop residue for improving input use efficiency and agricultural sustainability. Sustainablility. 2020;12:9808. DOI: 10.3390/su/2239808
  63. 63. Chivenge P, Rubianes F, Van Chin D, Van Thach T, Khang VT, Romasanta RR, Van Hung N et al. Rice straw incorporation influences nutrient cycling and soil organic matter. Sustainable Rice Straw Management Gummert, N. Van Hung, P. Chivenge, and B. Douthwaite (ed.) Switzerland, Cham: Springer; 2019. pp. 131-144. DOI: 10.1007/978-3-030-32373-8_8
  64. 64. Ngan N, Chan F, Nam T, Van Thao H, Maguyon-Detras MC, Hung DV, Cuong DM. Anaerobic digestion of rice straw for biogas production. In: Sustainable Rice Straw Management. Gummert, M., N. Van Hung, P. Chivenge, and B. Douthwaite (ed.) Switzerland, Cham: Springer; 2019. pp. 65-92
  65. 65. Prasad S, Kumar S, Sheetal K, Venkatramanan V. Global climate change and biofuels policy: Indian perspectives. In: Venkatramanan V, Shachi S, editors. Global Climate Change and Environmental Policy: Agriculture Perspectives. Singapore, Asia: Springer Nature Singapore Pte Ltd; 2020. pp. 207-226
  66. 66. Shyamsundar P, Springer NP, Tallis H, Polasky S, Jat ML, Sidhu HS, et al. Fields on fire: Alternatives to crop residue burning in India. Science. 2019;365:536-538. DOI: 10.1126/science.aaw4085
  67. 67. Grade S, Berling E, Blanco B, Caceres R, Checa JG, Di Lonardo S, et al. Circularity and/or valorization of biomass: crop residue, by-products and extraction of materials. Circular Horticulture. 2019;2019:1-14
  68. 68. Muth DJ, Bryden KM. An integrated model for assessment of sustainable agricultural residue removal limits for bioenergy systems. Environmental Modelling & Software. 2013;39:50-69
  69. 69. Ameur W, Frija A, Abdeladhim MA, Thabet C. Patterns of use of residue biomass in cereal-sheep production systems of North Africa: Case of Tunisia. Agriculture. 2021;11:612. DOI: 10.3390/agriculture 11070612
  70. 70. Jiang D, Zhuang D, Fu J, Huang Y, Wen K. Bioenergy potential from crop residues in China: Availability and distribution. Renewable and Sustainable Energy Reviews. 2012;16:1377-1382
  71. 71. Wang Z-W, Lei T-Z, Yan X-Y, Li Y-L, He X-F, Zhu J-L. Assessment and utilization of agricultural residues in HenanProvince China. BioResources. 2012;7(3):3847-3861
  72. 72. HPDRC. Comprehensive Utilization of Agricultural Residues in Henan Province. Zhengzhou, China: Henan Province Development Commission; 2011
  73. 73. Huang HX, Li ST, Li XL. Analysis on the status of organic fertilizer and its development strategies in China. Soil Fertilizer (TurangFeiliao). 2006;1:3-8
  74. 74. Baudron F, Delmotte S, Corbeels M, Herrera JM, Tittonell P. Multi-scale trade-off analysis of cereal residue use for livestock feeding vs. soil mulching in the Mid-Zambezi Valley, Zimbabwe. Agricultural System. 2015;134:97-106
  75. 75. Jaleta M, Kassie M, Shiferaw B. Tradeoffs in crop residue utilization in mixed crop–livestock systems and implications for conservation agriculture. Agricultural Systems. 2013;121:96-105
  76. 76. Erenstein O. Crop residue mulching in tropical and semi-tropical countries: An evaluation of residue availability and other technological implications. Soil and Tillage Research. 2002;67:115-133
  77. 77. Alemu T, Chairatanayuth P, Vijchulata P, Tudsri S. Production and utilization of crop residues in three agroecological zones of Eastern Shoa zone, Ethiopia. Kasetsart Journal (Natural Science). 2006;40:643-651
  78. 78. Wirsenius S. The biomass metabolism of the food system: A model-based survey of the global and regional turnover of food biomass. Journal of Industrial Ecology. 2003;7:47
  79. 79. Weiser C, Zeller V, Reinicke F, Wagner B, Majer S, Vetter A, et al. Integrated assessment of sustainable cereal straw potential and different straw-based energy applications in Germany. Applied Energy. 2013;114:749-762. DOI: 10.1016/j.apenergy.2013.07.016
  80. 80. Scarlat N, Martinov M, Dallemand J-F. Assessment of the availability of agricultural crop residues in the European Union: Potential and limitations for bioenergy use. Waste Management. 2010;30:1889
  81. 81. Ericsson K, Nilsson L. Assessment of the potential biomass supply in Europe using a resource-focused approach. Biomass and Bioenergy. 2006;30:1
  82. 82. Patel M, Zhang X, Kumar A. Techno-economic and life cycle assessment on lignocellulosic biomass thermochemical conversion technologies: A review. Renewable Sustainable Energy Review. 2016;53:1486-1499
  83. 83. Kretschmer B, Allen B, Hart K. Mobilising Cereal Straw in the EU to Feed Advanced Biofuel Production. London: IEEP; 2012
  84. 84. Urosevic DM, Gvozdenac-Urosevic BD. Comprehensive analysis of a strawfiredpower plant in the province of Vojvodina. Thermal Science. 2012;16:S97eS106
  85. 85. Peidong Z, Yanli Y, Yongsheng T, Xutong Y, Yongkai Z, Yonghong Z, et al. Bioenergy industries development in China: Dilemma and solution. Renewable and Sustainable Energy Reviews. 2009;13:2571e2579
  86. 86. Purohit P. Economic potential of biomass gasification projects under clean development mechanism in India. Journal of Cleaner Production. 2009;17:181e193
  87. 87. Chum H, Faaij A, Moreira J, Berndes G et al. Bioenergy. In: IPCC Special Report on Renewable Energy Sources and Climate Change Mitigation [O. Edenhofer, R. Pichs-Madruga, Y. Sokona, K. Seyboth, P. Matschoss, S. Kadner, T. Zwickel, P. Eickemeier, G. Hansen, S. Schlömerand, C. von Stechow (eds)]. Cambridge University Press: Cambridge; 2011
  88. 88. Kline KL, Oladosu GA, Wolfe AK, Perlack RD, Dale VH, McMahon M. Biofuel Feedstock Assessment for Selected Countries. Oak Ridge TN: Oak Ridge National Laboratory; 2008. p. 210
  89. 89. Panoutsou C, Langeveld H, Vis M, Lammens TM, Askew M, Carrez D et al. D8.2 Vision for 1 billion dry tonnes D8.2 Vision for 1 billion dry tonnes lignocellulosic biomas as a contribution to biobased economy by 2030 in Europe. S2Biom. 2016. Available from: https://edepot.wur.nl/517794
  90. 90. Gylling M, Jørgensen U, Bentsen NS, Kristensen IT, Dalgaard T, Felby C, et al. The + 10 Million Tonnes Study: Increasing the Sustainable Production of Biomass for Biorefineries. Copenhagen: Department of Food and Resource Economics, University of Copenhagen; 2013
  91. 91. Larsen SU, Bruun S, Lindedam J. Straw yield and saccharification potential for ethanol in cereal species and wheat cultivars. Biomass and Bioenergy. 2012;45:239
  92. 92. Thomsen TP, Ravenni G, Holm JK, Ahrenfeldt J, Hauggaard-Nielsen H, Henriksen UB. Screening of various low-grade biomass materials for low temperature gasification: Method development and application. Biomass and Bioenergy. 2015;79:128-144
  93. 93. UCS (Union of Concerned Scientists). The Promise of Biomass: Clean Power and Fuel—If Handled Right. Cambridge: UCS; 2012
  94. 94. USDA (U.S. Department of Agriculture). Census of Agriculture: Summary and State Data. Washington, DC: USDA; 2009
  95. 95. Jekayinfa SO, Pecenka R, Orisaleye JI. Empirical model for prediction of density and water resistance of corn cob briquettes. International Journal of Renewable Energy Technology. 2019;10:212-228
  96. 96. Orisaleye JI, Jekayinfa SO, Adebayo AO, Ahmed NA, Pecenka R. Effect of densification variables on density of corn cob briquettes produced using a uniaxial compaction biomass briquetting press. Energy Sources, Part A: Recovery, Utilization, and Environmental Effects. 2018;40:3019-3028
  97. 97. Orisaleye JI, Jekayinfa SO, Pecenka R, Onifade TB. Effect of densification variables on water resistance of corn cob briquettes. Agronomy Research. 2019;17:1722-1734
  98. 98. Fogarassy C, Toth L, Czikkely M, Finger DC. Improving the efficiency of pyrolysis and increasing the quality of gas production through optimization of prototype systems. Resources. 2019;8:182
  99. 99. Tursi AA. Review on biomass: Importance, chemistry, classification, and conversion. Biofuel Research Journal. 2019;22:962-979
  100. 100. Adebayo AO, Jekayinfa SO, Ahmed NA. Kinetic study of thermophilic anaerobic digestion of cattle manure in a continuously stirred tank reactor under varying organic loading rate. ARPN Journal of Engineering Applied Science. 2018;13:3111-3118
  101. 101. Aigbodion AI, Bakare IO, Fagbemi EA, Abolagba EO, Omonigho B, Ayeke PO, et al. Viability of biogas production from manure/biomass in Nigeria using fixed dome digester. University Journal of Agricultural Research. 2018;6:1-8
  102. 102. Dahunsi SO, Oranusi S, Efeovbokhan VE, Zahedi S, Ojediran JO, Olayanju A, et al. Biochemical conversion of fruit rind of Telfairiaoccidentalis (fluted pumpkin) and poultry manure. Energy Sources, Part A: Recovery, Utilization, and Environmental Effects. 2018;40:2799-2811
  103. 103. Deng YY, Koper M, Haigh M, Dornburg V. Country-level assessment of long-term global bioenergy potential. Biomass and Bioenergy. 2015;2015(74):253-267
  104. 104. Royse DJ, Baars J, Tan Q. Current overview of mushroom production in the world. In: Zied DC, Pardo-Giminez A, editors. Edible and Medicinal Mushrooms: Technology and Applications. Hoboken: JohnWiley& Sons Ltd; 2017. pp. 5-13
  105. 105. Grimm D, Wosten HAB. Mushroom cultivation in the circular economy. Applied Microbiology and Biotechnology. 2018;102:7795-7803. DOI: 10.1007/300253-018-9226-8
  106. 106. Hu Y, Mortimer PE, Hyde KD, Kakumyan P, Thongklang N. Mushroom cultivation for soil amendment and bioremediation. Circular. Agricultural Systems. 2021;1:11
  107. 107. Raman J, Lee S-K, Im J-H, Oh M-J, Oh Y-L, Jang K-Y. Current prospects of mushroom production and industrial growth in India. Journal of Mushrooms. 2018;16(4):239-249
  108. 108. Kazige OK, Chuma GB, Lusambya AS, Mondo JM, Balezi AZ. Valorizing staple crop residues through mushroom production to improve food security in eastern Democratic Republic of Congo. Journal of Agriculture and Food Research. 2022;8:100285
  109. 109. Adjapong AO, Ansah KD, Angfaarabung F, Sintim HO. Maize residue as a viable substrate for farm scale cultivation of Oyster mushroom (Pleurotusosteatus). Advances in Agriculture. 2015;2015:1-6. DOI: 10.1155/2015/213251
  110. 110. Royse DJ. Cultivation of Oyster Mushrooms. Extension Bulletin, College of Agricultural Sciences, The Pennsylvania State University, University Park, PA; 2003
  111. 111. Wakchaure GC. Production and Marketing of Mushrooms: Global and national scenario. In: Singh M, Vijay B, Kamal S, Wakchaure GC, editors. Mushrooms Cultivation, Marketing and Consumption Global and National Scenario. Himachal Pradesh; 2011
  112. 112. Polat E, Uzun H, Topçuo B, Önal K, Onus AN. Effects of spent mushroom compost on quality and productivity of cucumber (Cucumissativus L.) grown in greenhouses. African Journal of Biotechnology. 2009;8:176-180
  113. 113. Nasehi M, Torbatinejad NM, Zerehdaran S. Effect of solid-state fermentation by oyster mushroom (Pleurotusflorida) on nutritive value of some agro by-products. Journal of Applied Animal Research. 2017;45:221-226
  114. 114. Phan CW, Sabaratnam V. Potential uses of spent mushroom substrate and its associated lignocellulosic enzymes. Applied Microbiology and Biotechnology. 2012;96:863-873
  115. 115. Appels FVW, Dijksterhuis J, Lukasiewicz CE, Jansen KMB, Wösten HAB, Krijgsheld P. Hydrophobin gene deletion and environmental growth conditions impact mechanical properties of mycelium by affecting the density of the material. Scientific Reports. 2018;8:4703
  116. 116. Islam MR, Tudryn G, Bucinell R, Schadler L, Picu PC. Morphology and mechanics of fungal mycelium. Scientific Reports. 2017;7:13070
  117. 117. Jones MP, Huynh T, Dekiwadia C, Daver F, John S. Mycelium composites: A review of engineering characteristics and growth kinetics. Journal of Bionanoscience. 2017;11:241-257
  118. 118. Kulshreshtha S. Removal of pollutants using spent mushrooms substrates. Environmental Chemistry Letters. 2019;17:833-847
  119. 119. Paula FS, Tatti E, Abram F, Wilson J, O’Flaherty V. Stabilisation of spent mushroom substrate for application as a plant growth-promoting organic amendment. Journal of Environmental Management. 2017;196:476-486
  120. 120. Kumar K, Yadav AN, Kumar V, Vyas P, Dhaliwal HS. Food waste: A potential bioresource for extraction of nutraceuticals and bioactive compounds. Bioresources and Bioproceedings. 2017;4:1-14
  121. 121. Rafael Gomes-Araújo R, Martínez-Vázquez DG, Charles-Rodríguez AV, Rangel-Ortega S, Robledo-Olivo A. Bioactive compounds from agricultural residues, their obtaining techniques, and the antimicrobial effect as postharvest additives. International Journal of Food Science. 2021;2021:1-13
  122. 122. Jain S, Anal AK. Optimization of extraction of functional protein hydrolysates from chicken egg shell membrane (ESM) by ultrasonic assisted extraction (UAE) and enzymatic hydrolysis. Food Science and Technology. 2016;69:295-302. DOI: 10.1016/j.lwt.2016.01.057
  123. 123. Maysonnave GS, Mello RO, Vaz FN, Avila MM, Pascoal LL, Rodrigues ACT. Physicochemical characterization of by-products from beef cattle slaughter and economic feasibility of commercialization. Animal Science. 2020;42:e46545
  124. 124. Prado DMF, Almeida AB, Oliveira-Filho JG, Alves CCF, Egea MB, Lemes AC. Extraction of bioactive proteins from seeds (Corn, Sorghum, and sunflower) and sunflower byproduct: Enzymatic hydrolysis and antioxidant properties. Current Nutrition & Food Science. 2020;17(3):310-320. DOI: 10.2174/1573401316999200731005803
  125. 125. Kips L, De Paepe D, Bernaert N, Van Pamel E, De Loose M, Raes K, et al. Using a novel spiral-filter press technology to biorefine horticultural by-products: The case of tomato. Part I: Process optimization and evaluation of the process impact on the antioxidative capacity. Innovative Food Science & Emerging Technologies. 2016;38:198-205
  126. 126. Alongi M, Anese M. Re-thinking functional food development through a holistic approach. Journal of Functional Foods. 2021;81:104466
  127. 127. Silva LBAR, Pinheiro-Castro N, Novaes GM, et al. Bioactive food compounds, epigenetics and chronic disease prevention: Focus on early-life interventions with polyphenols. Food Research International. 2019;125:108646. DOI: 10.1016/j.foodres.2019.108646
  128. 128. Valencia-Mejía E, Batista KA, Fernández JJA, Fernandes KF. Antihyperglycemic and hypoglycemic activity of naturally occurring peptides and protein hydrolysates from easy-to-cook and hard-to-cook beans (Phaseolus vulgaris L.). Food Research Interferon. 2019;121:238-246. DOI: 10.1016/j.foodres.2019.03.043
  129. 129. Aguiar LM, Geraldi MV, Betim Cazarin CB, Marostica Junior MR. Chapter 11 - Functional food consumption and its physiological effects. In: Bioactive Compounds: Health Benefits and Potential Applications. M.R.S. Campos (editor) (Woodhead Publishing). 2019:205-225. DOI: 10.1016/b978-0-12-814774-0.00011-6
  130. 130. Daliu P, Santini A, Novellino E. A Decade of neutraceutical patents: where are we now in 2018. Expert Opinion on Therapeutic Patents. 2018;28(12):875-882. DOI: 10.1080/13543776.2018.1552260
  131. 131. Oliveira Filho JG, Braga ARC, de Oliveira BR, et al. The potential of anthocyanins in smart, active, and bioactive eco-friendly polymer-based films: A Review. Food Research International. 2021;142:10202
  132. 132. Reque P, Brandelli A. Encapsulation of probiotics and nutraceuticals: Applications in functional food industry. Trends in Food Science and Technology. 2021;114:1-10. DOI: 10.1016/j.tifs.2021.05.022
  133. 133. Ligianne Din Shirahigue LD, Ceccato-Antonini SR. Agro-industrial wastes as sources of bioactive compounds for food and fermentation industries. Ciência Rural, Santa Maria. 2020;50:e20190857
  134. 134. Dini I. Bio discarded from waste to resource. Food. 2021;10:2652. DOI: 10.3390/foods10112652
  135. 135. Martínez-Espinosa R. Introductory Chapter: A brief overview on fermentation and challenges for the next future. In: Martínez-Espinosa RM, editor. New Advances on Fermentation Processes. London, UK: IntechOpen; 2020
  136. 136. Shin H-Y, Kim S-M, Lee JH, Lim S-T. Solid-state fermentation of black rice bran with Aspergillus awamori and Aspergillus oryzae: Effects on phenolic acid composition and antioxidant activity of bran extracts. Food Chemistry. 2019;272:235-241. DOI: 10.1016/j.foodchem.2018.07.174
  137. 137. Silva J, Honorato da Silva FL, Santos Ribeiro JE, Nóbrega de Melo DJ, Santos FA, Lucena de Medeiros L. Effect of supplementation, temperature and pH on carotenoids and lipids production by Rhodotorula mucilaginosa on Sisal bagasse hydrolyzate. Biocatalysis and Agricultural Biotechnology. 2020;30:101847. DOI: 10.1016/j.bcab.2020.101847
  138. 138. Golebiewska E, Kalinowska M. Agricultural residues as a source of bioactive substances—waste management with the idea of circular economy. Environmental Science Proceedings. 2021;9(1):2
  139. 139. Wenzel J, Samaniego CS, Wang L, Burrows L, Tucker E, Dwarshuis N, et al. Antioxidant potential of Juglans nigra, black walnut, husks extracted using supercritical carbon dioxide with an ethanol modifier. Food Science & Nutrition. 2016;5(2):223-232. DOI: 10.1002/fsn3.385
  140. 140. Ko J-Y, Ko M-K, Kim D-S, Lim S-B. Enhanced production of phenolic compounds from pumpkin leaves by subcritical water hydrolysis. Preventive in Nutritional Food Science. 2016;21:132-137
  141. 141. Mayanga-Torres PC, Lachos-Perez D, Rezende CA, Pradoc JM, Ma Z, Tompsett GT, et al. Valorization of coffee industry residues by subcritical water hydrolysis: Recovery of sugars and phenolic compounds. The Journal of Supercritical Fluids. 2017;120:75-85. DOI: 10.1016/j.supflu.2016.10.015
  142. 142. Marathe SJ, Jadhav SB, Bankar SB, Dubey KK, Singhal RS. Improvements in the extraction of bioactive compounds by enzymes. Current Opinion in Food Science. 2019;25:62-72. DOI: 10.1016/j.cofs.2019.02.009
  143. 143. Moreira MD, Melo MM, Coimbra JM, Reis KC, Schwan RF, Silva CF. Solid coffee waste as alternative to produce carotenoids with antioxidant and antimicrobial activities. Waste Management. 2018;82:93-99. DOI: 10.1016/j.wasman.2018.10.017
  144. 144. Sinha S, Singh G, Arora A, Paul D. Carotenoid production by Red Yeast isolates grown in agricultural and "Mandi" waste. Waste and Biomass Valorization. 2021;12(7):3939-3949. DOI: 10.1007/s12649-020-01288-8
  145. 145. Aguilo-Aguayo I, Walton J, Vinas I, Tiwari BK. Ultrasound assisted extraction of polysaccharides from mushroom by-products. LWT - Food Science and Technology. 2017;77:92-99
  146. 146. Piñeiro Z, Marrufo-Curtido A, Serrano MJ, Palma M. Ultrasound-assisted extraction of stilbenes from grape canes. Molecules. 2016;21:784
  147. 147. Zhou C, Wang Y. Recent progress in the conversion of biomass wastes into functional materials for value-added applications. Science and Technology of Advanced Materials. 2020;21(1):787-804. DOI: 10.1080/14686996.2020.1848213
  148. 148. Filip S, Pavlic B, Vidovic S, Vladic J, Zekovic Z. Optimization of microwave-assisted extraction of polyphenolic compounds from Ocimum basilicum by response surface methodology. Food Analytical Methods. 2017a;10(7):2270-2280. DOI: 10.1007/s12161-017-0792-7
  149. 149. Kulkarni V, Rathod V. Green process for extraction of mangiferin from Mangifera indica leaves. Journal of Biology. 2016;6:406-411
  150. 150. Gencdag E, Gorguc A, Yilmaz FM. Recent advances in the recovery techniques of plant-based proteins from agro-industrial byproducts. Food Review International. 2021;37(4):447-468
  151. 151. Isah S, Ozbay G. Valorization of food loss and wastes: Feedstocks for biofuels and valuable chemicals. Frontiers in Sustainable FoodSystem. 2020;4:82
  152. 152. Mouratoglou E, Malliou V, Makris DP. Novel glycerol-based natural eutectic mixtures and their efficiency in the ultrasound-assisted extraction of antioxidant polyphenols from agri-food waste biomass. Waste and Biomass Valorization. 2016;7:1377-1387
  153. 153. Sana B-O, Joudu I, Bhat R. Bioactives from agri-food wastes: Present insights and future challenges. Molecules. 2020;25:510. DOI: 10.3390/molecules25030510
  154. 154. McClements DJ, Ozturk B. Utilization of nanotechnology to improve the application and bioavailability of phytochemicals derived from waste streams. Journal of Agricultural Food Chemistry. 2021;70(23):6884-6900
  155. 155. Thakur J, Borah A. Microcapsules of bioactive compoundsfrom fruits and vegetables waste and their utilization: A review. Innovation. 2021;10(5):151-157
  156. 156. Kennedy DO, Wightman EL. Herbal extracts and phytochemicals: Plant secondary metabolites and the enhancement of human brain function. Advance Nutrition. 2011;2:32-50. DOI: 10.3945/an.110.000117
  157. 157. Friedman M. Analysis of biologically active compounds in potatoes (Solanum tuberosum), tomatoes (Lycopersiconesculentum), and jimson weed (Datura stramonium) seeds. Journal of Chromatography. A. 2004;1054:143-155
  158. 158. Kalogeropoulus N, Chiou A, Pyriochou V, Peristeraki A, Karathanos KT. Bioactive phytochemicals in industrial tomatoes and their processing byproducts. LWT- Food Science and Technology. 2012;49(2):213-216
  159. 159. Giovanetti MH, Nogueira A, de Oliveira CL, Wosiacki G. Chromatography—The Most Versatile Method of Chemical Analysis. Rijeka, Croatia: InTech; 2012
  160. 160. Valdés A, Burgos N, Jiménez A, Garrigós MC. Natural pectin polysaccharides as edible coatings. Coatings. 2015;5:865-886
  161. 161. Edris AE, Fadel HM. Investigation of the volatile aroma components of garlic leaves essential oil. Possibility of utilization to enrich garlic bulb oil. European Food Research and Technology. 2002;214:105-107
  162. 162. Benítez V, Mollá E, Martín-Cabrejas MA, Aguilera Y, López-Andréu FJ, Cools K, et al. Characterization of industrial onion wastes (Allium cepa L.): Dietary fibre and bioactive compounds. Plant Foods for Human Nutrition. 2011;66:48-57
  163. 163. Cáceres R, Malińska K, Marfà O. Nitrification within composting: A review. Waste Management. 2018;72:119-137
  164. 164. Debode J, De Tender C, Cremelie P, Shein Lee A, Kyndt T, Muylle H, et al. Trichoderma-inoculated miscanthus straw can replace peat in strawberry cultivation, with beneficial effects on disease control. Frontiers in Plant Science. 2018;9:213
  165. 165. Gervasi T, Pellizzeri V, Calabrese G, Di Bella G, Cicero N, Dugo G. Production of single cell protein (SCP) from food and agricultural waste by using Saccharomyces cerevisiae. Natural Product Research. 2018;32(6):648-653. DOI: 10.1080/14786419.2017.1332617
  166. 166. López-López N, López-Fabal A. Compost based ecological growing media according EU eco-label requirements. Scientia Horticulturae. 2016;212:1-10
  167. 167. Rogers MA. Organic vegetable crop production in controlled environments using soilless media. Horticultural Technology. 2017;27:166-170
  168. 168. Nayak A, Bhushan B. An overview of the recent trends on thewaste valorization techniques for food wastes. Journal of Environmental Management. 2019;2019(233):352-370
  169. 169. Li Z, Song Z, Singh B, Wang H. The impact of crop residue biochars on silicon and nutrient cycles in croplands. Science Total Environment. 2019;659:673-680. DOI: 10.1016/j.scitotenv.2018.12.381
  170. 170. Singh R, Babu J, Kumar R, Srivastava P, Singh P, Raghubanshi A. Multifaceted application of crop residue biochar as a tool for sustainable agriculture: An ecological perspective. Ecological Engineering. 2015;77:324-347. DOI: 10.1016/j. ecoleng.2015.01.011
  171. 171. de la Rosa JM, Rosado M, Paneque M, Miller AZ, Knicker H. Effects of aging under field conditions on biochar structure and composition: Implications for biochar stability in soils. Science of the Total Environment. 2018;613-614:969-976. DOI: 10.1016/j.scitotenv.2017.09.124
  172. 172. Katterer T, Roobroeck D, Andren O, Kimutai G, Karltun E, Kirchmann H, et al. Biochar addition persistently increased soil fertility and yields in maize-soybean rotations over 10 years in sub-humid regions of Kenya. Field Crops Research. 2019;235:18-26
  173. 173. Roobroeck D, Hood-Nowotny R, Nakubulwa D, Tumuhairwe J-B. Biophysical potential of crop residues for biochar carbon sequestration, and co-benefits, in Uganda. Ecological Applications. 2019;29:E01984
  174. 174. Minasny B, Malone BP, McBratney AB, Angeri DA, et al. Soil carbon 4 per mile. Geoderma. 2017;292:39-86
  175. 175. Jeffery S, Abalos D, Prodana M, Bastos AC, Van Groenigen JW, Hungate BA, et al. Biochar boosts tropical but not temperate crop yields. Environmental Research Letters. 2017;12(5):053001. DOI: 10.1088/1748-9326/aa67bd
  176. 176. Blanco-Canqui H. Biochar and soil physical properties. Soil Science Society of America Journal. 2017;81:687-711. DOI: 10.2136/sssaj2017.01.0017
  177. 177. Yu L, Gamliel DP, Markunas B, Valla JA. A promising solution for food waste: Preparing activated carbons for phenol removal from water streams. ACS Omega. 2021;6:8870-8883
  178. 178. Mohd Adib Yahya MA, Mansor MH, Zolkarnaini WAAW, Rusli NS, Aminuddin A, Mohamad K, et al. A brief review on activated carbon derived from agriculture by-Product. AIP Conference Proceedings. 2018;1972:030023
  179. 179. Pradham BK, Sandle NK. Effect of different oxidizing agent treatments on the surface properties of carbon. Carbon. 1999;4:391-400
  180. 180. Davis NE. Atherosclerosis-An inflammatory process. Journal of Insurance Medicine. 2005:37:72-75
  181. 181. Majewska T, Pudyszak K, Koziowski K. The effect of charcoal addition to diets for broiler performance and carcass parameters. Veterinary Medicine Zootechnika. 2011;55(77):30-32
  182. 182. Jiya EZ, Anyanwale BA, Ijaiya AT, Ugochukwu A, Tsado D. Effect of activated coconut shell charcoal meal on growth performance and nutrient digestibility of broiler chicken. British Journal of Applied Science and Technology. 2013;3(2):268-276
  183. 183. Durunna CS, Abatai UG, Uchegbu C. Performance evaluation of broiler chickens fed varying levels of raw African velvet tamarind, Icheku (Dialium guineense) wood charcoal as feed additive. In: Proceedings of 43rdAnnual Conference of the Nigerian Society for Animal Production, March 18th -22nd 2018. Owerri, Imo State, Nigeria; 2018. pp. 514-516
  184. 184. Dim CE, Akuru EA, Egom MA, Nnajofor NW, Ossai OK, Ukaigwe CG, et al. Effect of dietary inclusion of biochar on growth performance, haematology and serum lipid profile of broiler birds. Agro Science. 2018;17(2):8-16
  185. 185. Linhoss JE, Purswell JL, Streetand JT, Rowland MR. Evaluation of biochar as a litter amendment for commercial broiler production. Journal of Applied Poultry Research. 2019;28:1089-1098
  186. 186. Schmidt H-P, Hagemann N, Draper K, Kammann C. The use of biochar in animal feeding. PeerJ. 2019;7:e7373
  187. 187. Zhang X, Wang H, He L, Lu K, Sarmah A, Li J, et al. Using biochar for remediation of soilscontaminated with heavy metals and organic pollutants. Environmental Science Pollution. 2013;20:8472-8483
  188. 188. Moon DH, Hwang I, Chang YY, Koutsospyros A, Cheong KH, Ji WH, et al. Quality improvement of acidic soils by biochar derived from renewable materials. Environmental Science Pollution Controlled Series. 2017;24:4194-4199
  189. 189. Zwieten LV, Kimber S, Morris S, Chan KY, Downie A, Rust J, et al. Effects of biochar from slow pyrolysis of papermill waste on agronomic performance and soil fertility. Plant Soil. 2010;327:235-246
  190. 190. Chowdhury S, Sikder J, Mandal T, Halder G. Comprehensive analysis on sorptive uptake of enrofloxacin by activated carbon, and to enhance biodiesel production acting as a catalyst. Science Total Environment. 2019;665:438-452
  191. 191. Dehkhoda AM, West AH, Ellis N. Biochar based solid acid catalyst for biodiesel production. Applied Catalysis A: General. 2010;382:197-204
  192. 192. Yahya MA, Ngah CZC, Al-Qodah Z. Agricultural bio-waste materials as potential sustainable precursors used for activated carbon production: A review. Renewable and Sustainable Energy Reviews. 2015a;46:218-235. DOI: 10.1016/j.rser.2015.02.051
  193. 193. Hameed BH, Daud FBM. Adsorption studies of basic dye on activated carbon derived from agricultural waste: Hevea brasiliensis seed coat. Chemical Engineering Journal. 2008;139(1):48-55
  194. 194. Sugumaran PV, Susan P, Ravichandran P, Seshadri S. Production and characterization of activated carbon from banana empty fruit bunch and Delonix regia fruit pod. Journal of Sustainable Energy & Environment. 2012;3(3):125-132
  195. 195. Amirza MAR, Adib MMR, Hamdan R. Application of agricultural wastes activated carbon for dye removal – an overview. MATEC Web of Conferences. 2017;103(06013):1-12
  196. 196. Saygılı H, Güzel F. High surface area mesoporous activated carbon from tomato processing solid waste by zinc chloride activation: Process optimization, characterization and dyes adsorption. Journal of Cleaner Production. 2016;113:995-1004
  197. 197. Sych NV, Trofymenko SI, Poddubnaya OI, Tsyba MM, Sapsay VI, Klymchuk DO, et al. Porous structure and surface chemistry of phosphoric acid activated carbon from Corncob. Applied Surface Science. 2012;261:75-82
  198. 198. Peng Y, Sun Y, Sun R, et al. Optimizing the synthesis of Fe/Al (Hydr)oxides-Biochars to maximize phosphate removal via response surface model. Journal of Cleaned Products. 2019;237:117770
  199. 199. Ballu DA, Abdul-Halim A, Kojo QA, Yakubu A. Chemical characteristics of groundnut and sheanut shell biochars as adsorbents and soil conditioners in the era of ecological sustainability. Journal of Biological Research & Biotechnology. 2022;20(1):1461-1472
  200. 200. Karri RR, Sahu JN. Modeling and optimization by particle swarm embedded neural network for adsorption of zinc (II) by Palm Kernel shell based activated carbon from aqueous environment. Journal of Environmental Management. 2018a;206:178-191
  201. 201. Karri RR, Sahu JN. Process optimization and adsorptionmodeling using activated carbon derived from palm oil kernelshell for Zn (II) disposal from the aqueous environment usingdifferential evolution embedded neural network. Journal of Molecular Liquids. 2018b;265:592-602
  202. 202. Hu Z, Srinivasan MP. Mesoporous high-surface-areaactivated carbon. Microporous and Mesoporous Materials. 2001;43:267-275
  203. 203. Okhwa Hwang O, Lee S-R, Cho SS, Kyoung S, et al. Efficacy of different biochars in removing odorous volatile organic compounds (VOCs) emitted from swine manure. ACS Sustainable Chemical Engineering. 2018;6:14239-14247
  204. 204. Niazi L, Lashanizadegan A, Sharififard H. Chestnut oakshells activated carbon: Preparation, characterization and application for Cr (VI) removal from dilute aqueous solutions. Journal of Cleaner Production. 2018;185:554-561
  205. 205. Sathe PS, Adivarekar RV, Pandit AB. Valorization of peanut shell biochar for soil amendment. Journal of Plant Nutrition. 2021;2021:1-19. DOI: 10.1080/01904167.2021.1963771
  206. 206. Sattar MS, Shakoor MB, Ali S, Rizwan M, Niazi NK, Jilani A. Comparativeefficiency of peanut shell and peanut shell biocharfor removal of arsenic from water. Environmental Science Pollution Research. 2019;26(18):18624-18635
  207. 207. Tomul F, Yasin A, Burcu K, Trak D, Kendüzler E, Lima EC, et al. Peanut shells-derived biochars prepared from different carbonization processes: Comparison of characterization and mechanism of naproxen adsorption in water. Science of the Total Environment. 2020;726:137828. DOI: 10.1016/j.scitotenv.2020.137828
  208. 208. Yu F, Sun L, Zhou Y, Gao B, Gao W, Bao C, et al. Biosorbents based on agricultural wastes for ionic liquid removal: An approach to agricultural wastes management. Chemosphere. 2016;165:94-99
  209. 209. Karam DS, Nagabovanalli P, Rajoo KS, Ishak CF, Abdu A, Rosli Z, et al. An overview on the preparation of rice husk biochar, factors affecting its properties, and its agriculture application. Journal of the Saudi Society of Agricultural Sciences. 2022;25:149-159
  210. 210. Phuong HT, Uddin M, Kato Y. Characterization of biochar from pyrolysis of rice husk and rice straw. Journal of Biobased Materials and Bioenergy. 2015;9:439-446
  211. 211. Hesas RH, Arami-Niya A, Wan Daud WMA, Sahu JN. Preparation and characterization of activated carbon from applewaste by microwave-assisted phosphoric acid activation: Application in methylene blue adsorption. BioResources. 2013;8:2950-2966
  212. 212. Ozdemir I, Şahin M, Orhan R, Erdem. Preparation and characterization of activated carbon from grape stalk by zinc chloride activation. Fuel Processing Technology. 2014;125:200-206
  213. 213. Ren J, Chen N, Wan L, Li G, Chen T, Yang F, et al. Preparation of high-performance activated carbon from coffee grounds after extraction of bio-oil. Molecules. 2021;26:257
  214. 214. Promraksa A, Rakmak N. Biochar production from palm oil mill residues and application of the biochar to adsorb carbon dioxide. Heliyon. 2020;6:e04019. DOI: 10.1016/j.heliyon.2020.e04019
  215. 215. Safana Aminu Aliyu SA, Abdullah N, Sulaiman F, Umar S. Combustion characteristics of palm pressed fibres biochar and subbituminous Malaysian coal. Malaysian Journal of Fundamental and Applied Sciences. 2018;14(3):334-337
  216. 216. Adilah Shariff A, Aziz NSM, Abdullah N. Slow pyrolysis of oil palm empty fruit bunches for biochar production and characterization. Journal of Physical Science. 2014;25(2):97-112
  217. 217. Rahayu DE, Karnaningroem N, Altway A, Slamet A. Utilization of oil palm empty fruit bunches biomass through slow pyrolysis process. IOP Conference Series. 2021;913:012018
  218. 218. Yasin J, Pravinkumar R. Production of activated carbon from bio-waste materials by chemical activation method. AIP Conference Proceedings. 2020;2225:070005
  219. 219. Chaves L, Fernandes JD, Mendes JS, Dantas ERB, Guerra HC, Tito GA, et al. Characterization of poultry litter biochar for agricultural use. SYLWAN. 2020;164(6):468-487
  220. 220. Shakya A, Agarwal T. Poultry litter biochar: An approach towards poultry litter management – a review. International Journal of Current Microbiology. 2017;6(10):2657-2668
  221. 221. Zhou Y, Lu J, Zhou Y, Liu Y. Recent advances for dyes removal using novel adsorbents: A review. Environmental Pollution. 2019;252:352-365
  222. 222. Ma YL, Matsunaka T. Biochar derived from dairy cattle carcasses as an alternative source of phosphorus and amendment for soil acidity. Soil Science and Plant Nutrition. 2013;59(4):628-641. DOI: 10.1080/00380768.2013.806205
  223. 223. Gunamantha IM, Widana GAB. Characterization the potential of biochar from cow and pig manure for geoecology application. IOP Conference Series. 2018;2018:131012055
  224. 224. Chen HY, Li WY, Wang JJ, Xu HJ, Liu YL, Zhang Z, et al. Adsorption of cadmium and lead ions by phosphoric acid-modified biochar generated from chicken feather: Selective adsorption and influence of dissolved organic matter. Bioresource Technology. 2019;292:121948
  225. 225. Zhang C, Alexis WD, Li H, Guo M. Use of poultry litter derived biochar as litter amendment to control ammonia emissions. In: ASABE Annual International Meeting. Orlando, FL; 2016a
  226. 226. Zdravkov BD, Čermák JJ, Šefara M, Janku J. Pore classification in the characterization of porous materials: A perspective. Central European Journal of Chemistry. 2007;5(2):385-395. DOI: 10.2478/s11532-007-0017-9
  227. 227. Marsh H, Rodriguez-Reinoso F. Activated Carbon. 1st ed. New York: Elsevier Science and Technology Books; 2006
  228. 228. Budi E, Nasbey H, Yuniarti BDP, Nurmayatri Y, Fahdiana J, Budi AS. Pore structure of the activated coconut shell charcoal carbon. AIP Conference Proceedings. 2014;1617:130. DOI: 10.1063/1.4897121
  229. 229. Bouchelta C, Medjram MS, Bertrand O, Bellat J-P. Preparation and characterization of activated carbon from datestones by physical activation with steam. Journal of Analytical and Applied Pyrolysis. 2008;82:70-77
  230. 230. González JF, Román S, Encinar JM, Martínez G. Pyrolysis of various biomass residues and char utilization for theproduction of activated carbons. Journal of Analytical Applied Pyrolysis. 2009;85:134-141
  231. 231. Esmar Budi E, Umiatin H, Nasbey RA, Bintoro F. Activated coconut shell charcoal carbon using chemicalphysical activation. AIP Conference Proceedings. 2016;1712:050003. DOI: 10.1063/1.4941886
  232. 232. Adinata D, Wan Daud WMA, Aroua MK. Preparationand characterization of activated carbon from palm shell bychemical activation with K2CO3. Bioresource Technology. 2007;98:145-149
  233. 233. Tseng R-L. Physical and chemical properties and adsorptiontype of activated carbon prepared from plum kernels by NaOHactivation. Journal of Hazardous Materials. 2007;147:1020-1027
  234. 234. Danish M, Hashim R, Ibrahim MNM, Sulaiman O. Effect of acidic activating agents on surface area and surface functional groups of activated carbons produced from Acaciamangium wood. Journal of Analytical and Applied Pyrolysis. 2013;104:418-425
  235. 235. Filip S, Pavlić B, Vidović S, Vladić J, Zeković Z. Optimization of microwave-assisted extraction of polyphenolic compounds from Ocimum basilicum by response surface methodology. Food Analytical Methods. 2017b. DOI: 10.1007/s12161-017-0792-7
  236. 236. Karagoz S, Tay T, Ucar S, Erdem M. Activated carbonsfrom waste biomass by sulfuric acid activation and their use onmethylene blue adsorption. Bioresource Technology. 2008;99:6214-6222
  237. 237. Kyzas GZ, Deliyanni EA, Matis KA. Activated carbons produced by pyrolysis of waste potato peels: Cobalt ions removal by adsorption. Colloids and Surfaces, A: Physicochemical and Engineering Aspects. 2016;490:74-83
  238. 238. Yahya MA, Al-Qodah Z, Ngah CWZ. Agricultural biowaste materials as potential sustainable precursors used for activated carbon production: A review. Renewable Sustainable Energy Review. 2015b;46:218-235
  239. 239. Zhang S, Tao L, Zhang Y, Wang Z, Gou G, Jiang M, et al. Powder Technology. 2016b;295:152-160

Written By

Cosmas Chikezie Ogbu and Stephen Nnaemeka Okey

Submitted: 04 November 2022 Reviewed: 28 November 2022 Published: 08 February 2023