Open access peer-reviewed chapter

Characterization, Modeling and the Production Processes of Biopolymers in the Textiles Industry

Written By

Basel Younes

Submitted: 15 November 2020 Reviewed: 26 February 2021 Published: 30 March 2022

DOI: 10.5772/intechopen.96864

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Edited by Brajesh Kumar

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The current chapter is focused on biopolymers and Bionanocomposite as environmentally friendly materials, modeling of the production processes, and coating of bio-textiles. Different industries use biopolymers and Bionanocomposite in for the current environmental applications. Furthermore, composition and classification of biopolymers, the theoretical methods, and factorial experimental designs (FED) for optimization and modeling processes of the environmentally friendly textiles used as an alternative to traditional chemical textile products with zero to low environmental footprint are studied at acceptable cost. This chapter will also describe the novel optimization, experimental factorial design, and how the novel modeling methods will help less experienced polymer designers in taking the best experimental decision controlled by the design factors. It also discusses how the fully biodegradable polymers support the industry by decreasing the processing energy, material and manufacturing costs. Finally there are an overview of the current and future developments of biodegradable polymers applications in modern bio-textiles industries.


  • biodegradable textiles
  • biopolymers
  • coating
  • textiles industry

1. Introduction

The worldwide production of non-renewable textiles has increased, and textile producer are searching for solutions to overcome the waste problem [1]. There is a new generation of bio- textile materials based on petroleum, animal sources or agricultural [2] with a reasonable solution [3]. Micro-organisms (such as fungi and bacteria) broke down the biopolymers in the environment; such as a cotton fiber [4].

Table 1 [5] illustrates how degradation results are dependent on biodegradation type, the converted substrate, and residue makeup, with full degradation. Biodegradation happens within the biosphere, the organic chemicals are changed to simpler compounds and mineralized.

Original substrateBiodegradation TypeConverted into
PolymerAerobicCO2& H2O & (Biomass & Residue)
AnaerobicCH4& CO2& H2O & (Biomass & Residue)

Table 1.

Degradation results depending on biodegradation type [5].

Researchers have established many standardized testing procedures for the evaluation of the compost-ability and biodegradability of polymers using mixed cultures [6, 7, 8, 9, 10, 11]. Others have studied the effects of blend ratios on the degradation process on biopolymers [12, 13, 14]. The life cycle analysis is one of the methods simulating the development of biopolymers, with green fibers having a shorter life cycle than those that are oil-based. A green life cycle is given in Figure 1 [15].

Figure 1.

Life cycle of compos-table biodegradable fibers [15].

Biodegradable polymers are smart polymers which are currently being used in many fields such as tissue culturing, biomedical, agriculture, food and intelligent textiles [16, 17]. Considering environmental hazards [18], the main factors controlling the market scope and size of biodegradable polymers are material properties and cost [19]. Plasticizers are added to biopolymers during the extrusion process to decrease the intermolecular hydrogen bonds, to limit microbial growth, and to stabilize product properties [20]. The degradation rate of blended bio-polymers set the degradability of the produced mix [21]. Bio-materials take a key role in the of nanotechnology improvement as friendly materials. Nanomaterials have attracted considerable attention in medical delivery applications [22]. Classification and composition of biodegradable polymers will be briefly discussed; their applications in modern bio-textiles as well as textiles. Furthermore, modeling of biopolymers’ melt spinning process and factorial experimental design, optimization of the production processes for intelligent bio-fibers via statistical experimental design (SED), forecasting program for the fiber extrusion, as well as the future applications of biodegradable polymers in the modern textiles industry are also presented.

Electro-spinning of biopolymers has gained substantial attention in the last two decades, triggered mainly by the potential applications of electro-spun nanofibers in nanoscience and nanotechnology for tissue engineering [23]. Tissue engineering is a advanced technology, electrically conductive biodegradable composites are used in tissue engineering and bioelectronics [24].


2. Biodegradable polymers, classification and composition

Biopolymers are made from the agro-polymers (starch and cellulose), or are obtained by microbial production such as the polyhydroxyalkanoates. In polyhydroxybutyrate production, sugarcane, mustard, switch grass and corn have been recognized as candidates for genetic modification. Some polyhydroxybutyrate types polymerized chemically from agro-resources or chemical synthesis [25]. Classification of biopolymers and their origins are listed in Table 2 [3].

Biopolymers classification
ProteinsGelatine, casein, silk and woolAromatic PolyestersPolybutylene succinate terephthalate
PolysaccharidesStarch, cellulose, lignin and chitinAliphatic PolyestersPolyglycolic acid, Polybutylene succinate and polycaprolactone
LipidsCastor Oil,Plate Oil and animal fatsAliphatic-Aromatic
1- micro-organism or plants
1-polyhydroxyalcanoates, poly-3-hydroxybutyratePolyvinyl-alcohols
2- bio derived monomers2- polylactic acidModified PolyolefinPolyethylene or polypropylene& specific agents

Table 2.

Classification of biopolymers [3].

Biodegradable polymers are produced from aliphatic (linear) highly amorphous, flexible polymers and aromatic rings semi-crystalline, rigid polymers. The classification, development and synthesis of the main bio-based polymer types from biomass and microbial production, or from renewable resources are listed in Figure 2 [26, 27]. Aliphatic-aromatic copolymers can be synthesized and used in biomedical and agricultural applications by employing non-woven technology to produce products such as disposable wipes, refuse bags, seed mats and erosion control items [28, 29].

Figure 2.

Classification and development of bio-based polymers [26, 27]. PCL – polycaprolactone; PBS – polybutylene succinate; PTT– polytrimethyleneterephthalate; PBSA – polybutylene succinate adipate; PHH – polyhydroxyhexanoate; AAC – Aliphatic-Aromatic Co-polyesters; PHV – polyhydroxyvalerate; PET – polyethylene terephthalate; PLA – polylactic acid; PBAT – polybutylene adipate/terephthalate; PHA – polyhydroxyalkanoates; PTMAT– polyethylene adipate/terephthalate; PHB – polyhydroxybutyrate (type of PHA); PBT– polybutylene succinate; PHBV, PHBHx- types of PHA; PUR– polyurethanes.


3. Techniques for the preparation and synthesis of biopolymers

Due to biopolymers’ biodegradability and substantially, their applications are environmentally friendly [30]. Biopolymers properties influence the shelf-life and the product’s biodegradability. The possibility of increasing the strength of bio-polymers and bio-composites have been studied without decreasing the biodegradability [31].

Poly (butylene succinate-co-butylene terephthalate) co-polyesters have much better thermal stabilities in nitrogen compare to air [32]. It was reported that “Poly(butylene succinateco- ethylene succinate-co-ethylene terephthalate)“can be polymerized from three pre-polymers of ethylene succinate, butylene succinate, and ethylene terephthalate by direct poly-condensation [33]. An ideal random copolymer (Poly(butylene terephthalate-succinate-adipate) from aliphatic units (BA and BS) has a rubber-like tenacity curve [34]. Aliphatic aromatic copolyester (AAC) could potentially modify the basic BTA (1,4-butanediol, adipic acid, and terephthalic acid) structure and may become commercialized [35, 36]. Development of biodegradable aliphatic-aromatic co-polyesters began with the study of different modes of degradation [37, 38]. Aliphatic biopolymers are biodegradable and sensitive to hydrolysis; their flexible chain fits easily into the active site of an enzyme [39]. Aromatic biopolymers have favorable physical properties such as resistance to bacterial, fungal and hydrolysis attack [40] but degrade if they are co-polymerized with aliphatic bio-polymers [41]; breaking down by means of hydrolytic or/and enzyme degradation [42]. It was reported that inclusion and/or incorporation of aromatic monomer groups in the aliphatic polyesters’ main chain, can potentially enhance their mechanical properties [43]. The randomness and the length of the polymer chains aid in understanding the biodegradation behavior for aliphatic-aromatic co-polyesters [44]. Polyester-based nano-particulates could be easily prepared by solvents diffusion or evaporation methods. The degradability of the oligomers would decrease by increasing chain length [45], thus the amorphous part of the polymer would become that which is degraded [46].


4. Biopolymer and industrial applications

Biodegradable polymers used widely in industries such as textiles, packaging, fast-food container and packaging, paper coating, agriculture mulch films, medical products, tubes, lawn and garden waste bags, disposable wipes, erosion control, biologically-based resins, car parts, glass fibers agents, as well as coatings and adhesives [3, 47, 48]. Various blending ratios of regular and waxy corn starches with co-polyester were extruded into loose-fill foams [49]. PCL (polycaprolactone) are used to made spun fibers, scaffold fibroblasts and myoblasts for soft tissue engineering [15]. Natural biopolymer-based films and the packaging materials have been studied [50, 51]. Ochratoxin-A as well as amycotoxinis a common food contaminant that enters the human body through the consumption of improperly stored food products and can be used as a electrochemical biosensor [52]. Polysaccharide and protein based biopolymers can be utilized as coatings to enhance the fruits and vegetables quality; The medical biopolymers applications are [53] include extracorporeal (i.e., artificial kidneys, fluid lines, dialysis membranes, catheters, wound dressings, artificial skin, etc), temporary implants (i.e., degradable sutures, as well as arterial stents, tissue/cell transplants’ scaffolds, temporary vascular grafts, etc), and permanently implanted devices. Biopolymer fibers with typical morphology find applications in bone tissue engineering [54] and as a degradable nano-fiber [55]. Wound dressing materials must be biocompatible, anti-bacterial, prevent infection, and provide a suitable moist environment [56, 57]. Chitosan complexed with gelatin has been useful as a surgical dressing at a ratio of 3:1 (chitosan:gelatin), as it stimulates hemostasis and accelerates tissue regeneration [58, 59]. Their fabrication provides appropriate biodegradability and excellent cell adhesion activity, both useful in making a novel and elastomeric bioactive vascular tissue scaffold [60]. A fiber based on chitosan and starch which was loaded with drug has had successful applications in drug delivery [61]. Various fabrication methods have been employed in the preparation of bio-polymeric membranes and a film-casting process [62, 63].


5. Biopolymers and biodegradable textiles industry

The textile industry has played a important role in the exchanging of goods and impacted by novel techniques through the development of more environmentally friendly processes [64, 65, 66, 67]. Many biodegradable fibers may be natural, regenerated or synthetic such as Ingeo (Natureworks), LLC produced from corn, a biodegradable thermoplastic polyatide (PLA); Lenpur produced from wood pulp of harvested white pine tree clippings; and Modal and Tencel/Lyocell produced by Lenzing from wood pulp of beech and eucalyptus trees, and biodegradable aliphatic/aromatic multi-block co-polyesters. The largest application of alginates in textiles can be found in textile printing, the spinning and weaving of temporary fibers from calcium alginate [15]. Bio-based fibers like X-Static, Meryl Skinlife, Diolen Care, Trevira Bioactive are enriched with innovative antimicrobial products such as technical products, working uniforms, sportswear [68].

5.1 Fibers industry and biodegradable polymers

The melt spinning processing technologies with availability of biodegradable materials along have aided in qualitative and quantitative improvements [69]. The fibers reinforcing improve the relationship between the process parameters and the material properties [70]. Many natural fibers added to biopolymers as reinforcements (flax, cellulose acetate, bamboo, pineapple, ramie, kenaf, henequen, jute, sisal, and hemp); improving the strength without affecting the biodegradability [71]. Fibers of the poly(β-hydroxybutyrate) were produced via multistage melt-extrusion as well as gel-spinning [72]. The dry-jet wet spinning method was used to extrude the cellulose/NH3/NH4SCN solution [15]. By “dry-jet wet spinning” and using a cellulose/hydrolyzed starch-grafted-polyacrylonitrile solution, the mechanical properties of Lyocell fibers were improved [73]. An extruded Lyocell fibers were reported have potential uses in filters, geo-textiles, surgical gauze [74]. Cellulose fibers are used for the design of intelligent, bioactive, and biocompatible composites [75]. Preparing sol–gel derived biodegradable SiO2 gel fibers [76] for drug release consists of three steps: an initial burst, followed by a diffusion-controlled release behavior, and finally a step with a slower release rate. By incorporating responsive hydrogels in textiles, the surface energy switches between hydrophilic/hydrophobic, with the results listed in Table 3 [77].

BiopolymerMonomerNatural originProduction Micro-organismHydrogelFiberCommercialized
CelluloseglucosePlants, Micro-organismA. xylinumYesWound covering
Hyaluronic acidN-acetyl-glucosaminVertebrats, StreptococciStreptococci, B. subtilisYesNoDermal fillers, Visco supplementation
γ-PGAGlutamic acidBacillus spp., Micro-organismBacillus spp.NoCosmetics, fertilizer, flocculant
SilkproteinBombyxmorii, spider, beeE. coli,YesYesCosmetics, cell adhesion scaffolds
CollagenproteinVertebratesYeastsYesYesScaffolds, Cosmetics
ChitosanN-aeetyl-glucosamin (partly deacylated)fungiYeast, bacteriaYesYesFlocculant, Filter membranes, Cosmetics, wound covering

Table 3.

Monomers, origin and fiber formation of smart biopolymers [77].

There is good compatibility between the chitosan obtained from shrimp shells and starch-based polymers when forming a chitosan/starch fiber. Some researchers have made fiber from starch and biodegradable glycerine-based polymers with/without PLA and glucitol, while others extrude high strength PLLA fibers. The type LA 0200 K of PLA is processed at a high speed spinning (draw ratio = 6)in a spin drawing [78]. A fiber from soya bean protein is crafted by forcing a globular protein to become a fiber forming protein; the fiber has to be cross-linked if fibrous products are to be obtained [79]. Fibrous materials are segregated into two basic groups, the first can be placed on the surface of materials (i.e., surgical covers, gauzes, diapers and tampons), and the second can be placed inside an organic tissue (i.e., surgical threads, tendons and ligament implants, meshes, stents, and vascular grafts).

5.2 Fabric industry and biodegradable polymers

Weaving, knitting, nonwoven web forming (carding, spun-bond and wet-laid) and nonwoven-bonding (stitch-bonding, needling, calendaring and hot air bonding) are fabric forming technologies. Biodegradable non-woven webs and disposable articles contain fibers such as cotton, hemp, milkweed floss, flax fiber, wool, silk, chitin and chicken feathers [80]. There are many examples in biodegradable nonwoven such as biodegradable cotton-based nonwovens (cotton/cellulose, or cotton/ biodegradable co-polyester) and (PTAT co-polyester and PLA). Cotton/(co-polyester/PP) nonwovens along with absorbency and flexural rigidity have suitable mechanical properties and they are better than that of cotton/co-polyester nonwovens [81, 82, 83].

Sanitary and medical textiles, geotextiles, filtration media, within the automotive industry, PLA based hair caps, Bionolle 3001 nonwovens, Landlok biodegradable erosion control coconut fibers mats, Kenaf fiber nonwovens, refuse bags, drain filters made from fine denier PLA nonwovens, and biodegradable filter materials are used for both air and liquids. A biodegradable thermoplastic polymer and a plasticizer could be used to produce a starch matrix of the finely attenuated fibers which could have applications as environmentally degradable nonwoven webs and articles [84].

Researchers have produced biodegradable cotton-based, nonwovens by using blends of cotton, flax and biodegradable thermoplastic fibers that act as binders [85]; Biodegradability was monitored, with 40% of the initial weight lost after 8 weeks composting [86]. To reduce the cost, researchers have made a pure nonwoven material from co-polyester by a direct melt-blowing process [87]. Woven tubes (3 to 6.5) mm are developed using Polyglactin 910 biodegradable yarn on a narrow width loom [88].

Biodegradable poly (L-lactide-co-caprolactone) fabrics of nano/micro- structured can be made Using CH2Cl2 as a solvent in electro-spinning. The electro-spun elastomeric nano-fiber fabric is used as a functional scaffold in tissue engineering (i.e., cardiovascular, muscular) [89]. The Belgian Textile Research Centre’s projects include: Noterefiga for bio-based comfort textiles, Bioagrotex for agro-textiles (agriculture, horticulture, gardening and construction), Green-Nano-Mesh for medical areas, Dura cover for woven PLA taped ground covers, Hortaflex and Weed Control for PLA based nonwovens, and the BiobasedFilbio project for knitted PLA insect screens for climate control.

There are various commercialized fabrics made from naturally derived biopolymers such as those found in the Ethical Fashion Forum in London: POLY Acid Ingeo bio fibers; QMilchfibers, Lenzing’s Modal fiber, Micro Modal fiber, Lyocell fiber, POLARTEC polyester, unique corn-based PLA fleece; and Cork shell made from cork to form high quality textiles for lightweight spring and summer jackets. Biopolymers based in intelligent and/or stimuli responsive polymeric systems have been developed and reported by researchers for the functional finishing of textiles [90]. Scientists proposed changes of the polymer backbone in a reversible formation of PLA-dye complexes [91]. Sorona is used in the coat fabric for jackets, trench coats and outerwear with its 37% renewably sourced plant-based components; they lose their wrinkles with one quick snapping motion. Bio-based fabrics made of wool and “BIOPHYL” or “TENCEL”. Some commercial products are made from spider silk [92] and could be used in the bullet-proof vests industry [15].

5.3 Fiber and fabric coatings and biodegradable polymers

Modification techniques of the biopolymer’s surface includes coating, oxidation by low-temperature plasma, and surfactant addition blending with various derivatives [93]. Cyclodextrins or linear carbohydrate biopolymers were attached to the textile to allow frequent use and washing [94]. Regenerated cellulose fibers were treated by plasma activation using a chitosan solution [95]. Cellulose was coated by chitosan nano-particles to reduce the cost and non-toxic methodology [75]. While studying their development as well as characterization, both the organic cotton based bandages and cotton were coated separately on the gauze structure using chitosan-sodium alginate polymer, calcium-sodium alginate polymer and subsequent mixtures of the two, thereby improving its antibacterial and wound healing properties [96]. For dyeing and printing, the dextrin derivative surfactant improves the whiteness and wetting properties of cotton fabrics [97]. The chemical surface treatments of jute fabrics involve bleaching, dewaxing, cyanoethylation, alkali treatment and vinyl grafting are used as reinforcing components in biodegradable matrix composites, which are environmentally friendly materials [98]. A Knitted Dacron graft made of polyethylene oxidepolylactic acid were coated with a polymeric biodegradable sealant [99]. Layer-by-layer electrostatic deposition is used to coat the material by adding dextran sulphate and chitosan to a soybean based polymer [100]. The functional finishing of the micro- and nano-sized hydrogels improve response times [101].

Nano-composites and nano-structured coatings improve mechanical strength and flexibility, temperature and moisture stability, as well as durability. “Metal Rubber”(Nano Sonic Inc.) combines the rubber and metal properties, and it is used in artificial muscles, electrically charged aircraft wings, and protective biopolymer clothing [102]. Hydrogel-based biopolymers are used for the functional finishing of textiles by surface modifying systems [103].


6. Case study: modeling of biopolymers’ melt spinning process

All the production process parameters must be controlled to ensure the quality and then the significant main factors must be analyzed [104]. Commercially, it is a challenge to develop a new competitive product [105]. Some research is based on statistical analysis, mathematical simulation and modeling of the processes of fiber formation, and examples of their post-processes have been reported in literature [106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116]. The practical software-based approach has improved the confidence benefits of experimental design and simulation [117]. Figure 3 shows a flow chart for the methodologies used for obtaining the program, starting from the data and statistical modeling methods and SED. Online quality control tools were utilized for prediction, measurement, correction as well as adjustment and feedback [118].

Figure 3.

The flow chart of the statistical method.

The aliphatic aromatic co-polyester fibers extrusion process was investigated in this work, and statistically modeled [119]. A linear biodegradable oil-based polymer (LAAC-flexibility component of Solanyl) and branched aliphatic-aromatic co-polyester (BAAC-Ecoflex F BX 7011) were used to study the effects of the extrusion process and the properties of fibers. The study describes the melt spinning of aromatic-aliphatic co-polyester depending on the extrusion thermal profile effect on as-spun fiber properties. The molten material flowed easily when the viscosity decreased and smoother extrudates were obtained at shear rates greater than 4.5 s-1 [120].

6.1 Factorial experimental design for melt spinning of biodegradable fibers

Factorial experimental design provides data about the optimization of the average response values in regards to the factor levels [121]. The STATGRAPHICS program is used to design the experiment random order matrix and to simulate the main data in one block experiments.

The studied factors for the fiber extrusion process include: speed of spin finish, quenching air speed, metering pump speed, and winding speed, as well as, melt-spinning or extrusion temperature. The analyzed levels of each parameter were listed in Table 4; the thirty-two trials matrix for the five control factors was applied for as-spun fibers analysis. Figure 4 shows an SEM photomicrograph of the cross-section and surface of the fibers; fibers had an acceptable uniform surface and possessed a uniform circular cross section.

Factor nameLevel
TMelt-Spinning Temperature, oC (LAAC)130145
Melt-Spinning Temperature, oC (BAAC)145160
MPSSpeed of Metering Pump, rpm (2.4 cc/rev))612
QASpeed of Quench Air, % (velocity m/sec)3550
SFSpeed of Spin Finish Pump, rpm (0.15 cc/rev)0.350.50
WSWinding Speed, m/min50100

Table 4.

Factors and the selected levels for the spinning experiments of as-spun fibers.

Figure 4.

The surface and cross section of the biodegradable fibers [119].

In this case study [122, 123, 124], several statistical tools were utilized for statistical analysis including the surface plot, normal probability plot, the main effect plot, pareto chart, interaction plot, as well as analysis of variance (ANOVA). Implementation of forecasting statistical methods plays a major role in creating a planning program and a plan for the production process regression. A detailed experimental arrangement of the calculated results of spin draw ratio, birefringence, drawability, die head pressure, crystallographic order as full-width half-maximum (FWHM), filament temperature averages, count, tensile properties, diameter, and thermal shrinkage was completed. According to the drawability characterization, biodegradable fibers (i.e., as-spun) should consist of a drawn construction and be conducive to orient along the fiber axis of the chain [125]. There is a clear relationship between the draw down ratio and the orientation of the fibers and having a significant effect on the drawability. In other words, the overall orientation of fibers was increased and the draw ratio decreased as the spin draw ratio increased. Temperature significantly influenced the spin (down) draw ratio and fiber drawability that affects the flow rate and tension value. To study the effects of the factors as well as their statistical significance an ANOVA study was conducted. A factor was considered to have a significant effect if the F ratio (an ANOVA statistic) was shown to be more than the statistical value (F /4.49/at the appropriate level α =0.05) or had P-value smaller than 0.05. The ANOVA results from the experiments are presented in Table 5.

Table 5.

ANOVA results of factor effects on the drawability.

The significance of factors were PWS > PMPS> PT in the drawability analysis, while no significant effect was observed due to other factors. The P-value (0.016) of T&WS is lower than 0.05 and therefore is significant. The most significant factors were T, MPS and WS. Metering pump speed was observed to have interaction with winding speed; the speeds’ relationship oriented the fiber chains as well as added different spin draw ratio, having an effect on drawability later. Multiple and individual regressions optimized for the quality required for various applications and identified the factors’ effects and interactions to determine the direction of those that are significant by using the estimated response surfaces. A twist was observed in the 3D surface response diagrams for T and WS (Table 5), thus the interaction is significant and agrees with the previous statistical results. This interaction will affect the structure of the as-spun fibers and help to extend the chains to achieve high orientation along the axis of fiber. The regression Eq. (1) was obtained from the analysis and forms the simplified models of the experimental data (coded values in Table 4). The regression equations forecast the fiber properties and accurately predict the properties in the final fibers produced. The mathematical regression model forms one of the basic source codes in the designed forecasting application, which will present the extrusion of aromatic-aliphatic co-polyester fiber.


Where: a, b, c, d, e, f b1–10, are statistical constants for the drawability calculated by the STATGRAPHICS program.

They were also affected by high extrusion speed at which the shear rate affects the morphological structure [126]. Employing the same technique, the overall orientation, spin draw ratio, crystallographic order, die head pressure, diameter, tensile properties, thermo-graphic measurement and thermal shrinkage were also analyzed and modeled. The statistical analysis models simulated the significant factors, their interactions, and gave useful results with some expected outliers which could be due to experimental and/or testing errors.

6.2 Forecasting program for the fiber extrusion

In the programming process, the relationship between the key inputs (factors) and the performance measures (responses) using factorial statistical experimental design technology are reported. The statistical data and regression formulas are represented as a computer application. Microsoft Visual Basic was used to write a forecasting program that could be utilized for the as-spun AAC fibers’ extrusion process. The program offers the management of regression models for responses based on statistical factorial design, design analysis and process simulation. Conversion and summarization of the C++ source code into a simple flow chart was completed (Figure 5).

Figure 5.

Schematic program process.

After selecting the polymer grade, the program requests the parameters’ values, calculates the values’ responses by using regression equations and then gives the results. The data from the input conditions was used to obtain the structural, mechanical and physical data. The program was designed as two windows. The first window is the input window for process conditions (Figure 6); the second interface is the output result window (Figure 7).

Figure 6.

The main input interface/window for process conditions input.

Figure 7.

The output interface/window for filament temperature in the machine’s cooling window and the fiber’s structural, mechanical and physical properties.

Each factor is represented as a record and it may be owned by more than one record, leading to a network-like structure. The multiple regression analysis and previous forecasting models provide a basis for identifying the relationship between process-input and process-output data; and formation of a source code to be used in the forecasting program. The 30 hole spinneret (diameter is 0.4 mm, l/d ratio is 1.2) was used. The programmed application powerfully supports product development, design process control, quality assurance and product performance evaluation; it displays data on the screen or sends data to a file or other devices. Figure 7 shows the output interface/window for filament temperature in the machine’s cooling window and the fiber’s structural, mechanical and physical properties. Each factor is represented as a record and relationships between other factors through a matrix design.


7. Textiles industry future and biodegradable polymers

Reusing and recycling properties are the main goals for the environmentally friendly textile industry [127]; saving time, cost, and materials. There are various methods in which bio-polymers are processed, such as polymerization, crystallization and manufacturing depending on the polymer’s nature and application [128]. Biomechanical engineering design of clothing products is still at the development stage. Biological health and psychological happiness are critical indexes reflecting quality of life. Bio-material processing and bio-garment simulation has grown from basic shape modeling to the modeling of cloth with complex physics and behaviors. Bio-textile engineering approach offers precise details of modeling cloth at a micro, the graphics software simulate the fabric to form the final deformation and animation. The acceptance of biopolymer materials as commonplace in textile industry require the passage of time. Biopolymers boast greater environmental consciousness than most modern technologies, as they have the potential to significantly reducing cost, energy and materials for future generations. Modeling crosses the boundaries of academia, science and industry [129].


8. Conclusion

This chapter reviewed the relationship between the bio-polymers and the modeling of the production processes in textile industry. The theoretical techniques and factorial experimental design together with the biopolymers’ classification and preparation methods open new field of the modern textiles, from fiber to fabric forming and coating technologies. Biopolymer use in the textile industry is an exciting and innovative area of research for scientists and researchers alongside textile and polymer engineers.

In the case study, results obtained should answer the fairly complex demands posed by multi-applications running concurrently with the application programs (or processes) in the computer. It is limited by the regions of the studied factors between the factor levels. The program’s results help in achieving a balance between the enhanced properties and the fiber cost while saving processing cost, material and the power required for enhancing fibers. After finishing the processes for modeled biodegradable fibers, the process conditions (process-input data) selected depends upon the user. The produced environmentally friendly, economical, energy saving fibers can be potentially utilized in textiles, agricultural, as well as horticultural applications.



I wish to express his deep appreciation to Mechatronics Department, Engineering Faculty, Kalamoon University &Textiles Department, FMEE, Damascus University.


  1. 1. Chandra R, Rustgi R. Biodegradable Biopolymers. Great Britain: Elsevier Science Ltd; 1998
  2. 2. Steinbüchel A. Biopolymers Vol. 10: General Aspects and Special Applications. Germany: Wiley-VCH; 2003
  3. 3. Smith R. Biodegradable Polymers for Industrial Applications. England: Woodhead Publishing Limited; 2005
  4. 4. Harzallah O, Drean J-Y. Macro and Micro Characterization of Biopolymers: Case of Cotton Fibre. In: Elnashar M, editor. Biopolymers. Croatia: Sciyo; 2010. p. 193-218
  5. 5. Bastioli C. Handbook of Biodegradable Polymers. Shawbury, UK: Rabra Technology; 2005
  6. 6. Standard guide for assessing the compostability of environmentally degradable plastics, D 6002-96. American Society for Testing and Materials, Washington, DC. 1996
  7. 7. Sawada H. ISO standard activities in standardization of biodegradability of plastics-development of test methods and definitions. Polymer degradation and Stability. 1998;59:365-70
  8. 8. Pavlov MP, Mano JF, Neves NM, Reis RL. Fibres and 3D mesh scaffolds from Biodegradable starch based blends: production and characterization. Macromolecular bioscience 2004;4 776-84
  9. 9. Chen Y, Wombacher R, Wendorff JH, Visjager J, Smith P, Greiner A. Design, Synthesis, and Properties of New Biodegradable Aromatic/Aliphatic Liquid Crystalline Copolyesters. Biomacromolecules. 2003;4(4):974-80
  10. 10. Han L, Zhu G, Zhang W, Chen W. Composition, Thermal Properties, and Biodegradability of a New Biodegradable Aliphatic/Aromatic Copolyester. Journal of applied polymer science. 2009;113(2):1298-306
  11. 11. Averous L. Biodegradable multiphase systems based on plasticized starch: a review. Journal of Macromolecular Science - Polymer Reviews. 2004;44(3):231-74
  12. 12. ASTM. D 5338, Test Method for Determining Aerobic Biodegradation of Plastic Material under Controlled Compositing Conditions. 1998
  13. 13. Sami J. Processing of the 4th Conference on Biogically Degradable Mterials. Presentation No D 95 1999 (Festung Marienberg, Würzburg, Germany)
  14. 14. Biresaw G, Carriere CJ. Compatibility and mechanical properties of blends of polystyrene with biodegradable polyesters. Composites: Part A. 2004; 35:313-20
  15. 15. Blackburn RS. Biodegradable and Sustainable Fibres. Cambridge, UK: Woodhead Publishing; 2005
  16. 16. Holding W. Biodegradable Polymer Supply Chains: Implications and Opportunities for Australian Agriculture. Australia Rural Industries Research and Development Corporation; 2004
  17. 17. Monsanto. Biopolymers to Give Cotton Fibers Synthetic-Like Qualities. U.S.A: Monsanto company; 2003
  18. 18. Thakore SI. Role of Biopolymers in Green Nanotechnology. In: Verbeek J, editor. Products and Applications of Biopolymers. Croatia: Tech; 2012. p. 119-40
  19. 19. Kalambur S, Rizvi SSH. Biodegradable and Functionally Superior Starch-Polyester Nanocomposites from Reactive Extrusion. Journal of Applied Polymer Science. 2005;96(4):1072-82
  20. 20. Crank M, Patel M, Marscheider-Weidemann F, Schleich J, Hüsing B, Angerer G. Techno-economic Feasibility of Large-scale Production of Bio-based Polymers in Europe (PRO-BIP)-Final Report Utrecht University& Fraunhofer ISI,Spain 2004
  21. 21. Amass W, Amass A, Tighe B. A review of biodegradable polymers. Polymer international. 1998;47:89-144
  22. 22. Singha K, Namgung R, Kim WJ. Polymers in Small-Interfering RNA Delivery. Nucleic Acid Therapeutics. 2011;21(3):133-47
  23. 23. Wanga X, Ding B, Li B. Biomimetic electrospun nanofibrous structures for tissue engineering. Mater Today (Kidlington). 2013;16(6):229-41
  24. 24. Shi G, Rouabhia M, Wang Z, Dao LH, Zhang Z. A novel electrically conductive and biodegradable composite made of polypyrrole nanoparticles and polylactide. Biomaterials. 2004;25:2477-88
  25. 25. Takiyama E, Fujimaki T. Biodegradable Plastics and Polymers. Amsterdam: Elsevier; 1994
  26. 26. Nolan-ITU. Environment Australia:Biodegradable Plastics- Development and Environmental Impacts. Nolan-ITU, East Kew, Victoria. 2002
  27. 27. Crank M, Patel M, Marscheider-Weidemann F, Schleich J, Hüsing B, Angerer G, et al. Techno-economic Feasibility of Large-scale Production of Bio-based Polymers in Europe: Technical Report EUR 22103 EN. European Science and Technology Observatory. 2005;European Communities
  28. 28. Ganesh K, Alp AH, Russell GR, inventorsBiodegradable Aliphatic-Aromatic Copolyesters, Methods of Manufacture, and Articles Thereof 03/24/2011
  29. 29. Eastman polymers for fibres. Eastman chemical company, USA2002
  30. 30. NIIR-board. The Complete Book on Biodegradable Plastics and Polymers (Recent Developments, Properties, Analysis, Materials & Processes). Delhi, India: Asia Pacific Business Press Inc.; 2006
  31. 31. Stevens ES. Green Plastics, Plastics and the Environment USA: Princeton University Press; 2001
  32. 32. Li F, Xu X, Li Q, Li Y, Zhang H, Yu J, et al. Thermal degradation and their kinetics of biodegradable poly(butylene succinate-co-butylene terephthate)s under nitrogen and air atmospheres. Polymer Degradation and Stability. 2006;91:1685-93
  33. 33. Deng L-M, Wang Y-Z, Yang K-K, Wang X-L, Zhou Q, Ding S-D. A new biodegradable copolyester poly(butylene succinate-co-ethylene succinate-co-ethylene terephthalate) Acta Materialia. 2004;52(20):5871-8
  34. 34. Shi XQ, Aimi K, Ito H, Ando S, Kikutani T. Characterization on mixed-crystal structure of poly(butylene terephthalate/succinate/adipate) biodegradable copolymer fibers. Polymer. 2005;46:751-60
  35. 35. Rolf-Joachim M, Ilona K, Wolf-Dieter D. Biodegradation of polyesters containing aromatic constituents. Journal of biotechnology. 2001;86(2):87-95
  36. 36. Witt U, Muller R-J, Deckwer W-D. New biodegradable polyester-copolyesters from commodity chemicals with favorable use properties. Journal of Polymers and the Environment. 1995;3(4):215-23
  37. 37. Park SS, Chae SH, Im SS. Transesterification and crystallization behavior of poly (butylene succinate)/poly( butylene terephthalate) block copolymers. Journal of Polymer Science, Part A: Polymer Chemistry 1998;36(1):147-56
  38. 38. Hayes RA. Aliphatic-aromatic copolyesters. US Patent 6485819. 2002
  39. 39. Pan P, Inoue Y. Polymorphism and isomorphism in biodegradable polyesters. Progress in Polymer Science. 2009(34):605-40
  40. 40. Ki HC, Park OO. Synthesis, characterization and biodegradability of the biodegradable aliphatic–aromatic random copolyesters. Polymer. 2001;42:1849-61
  41. 41. Tokiwa Y, Suzoki T, Appl J. Hydrolysis of copolyesters containing aromatic and aliphatic ester blocks by lipase. Journal of Applied Polymer Science. 1981;26(2):441-8
  42. 42. Xiong X, Tam K. Hydrolytic degradation of pluronic F127/poly (lactic acid) block copolymer nanoparticles. Macromolecules. 2004;37(34):25-30
  43. 43. Jin H-J, Lee B-Y, Kim M-N, Yoon J-S. Thermal and mechanical properties of mandelic acid-copolymerized poly(butylene succinate) and poly(ethylene adipate). Journal of Polymer Science, Part B: Polymer Physics. 2000;38:1504-11
  44. 44. Witt U, Müller R-J, Deckwer W-D. Studies on sequence distribution of aliphatic/aromatic copolyesters by high-resolution C nuclear magnetic resonance spectroscopy for evaluation of biodegradability. Makromol Chem Phys. 1996;197:1525-35
  45. 45. Muller RJ, Witt U, Rantze E, Deckwer WD. Architecture of biodegradable copolyestyers containing aromatic constituents. Polymer Degradation and Stability 1998;59:203-8
  46. 46. Massardier-Nageotte V, Pestre C, Cruard-Pradet T, Bayard R. Aerobic and anaerobic biodegradability of polymer films and physico-chemical characterization. Polymer Degradation and Stability. 2006;91:620-7
  47. 47. Herrmann AS, Nickel J, Riedel U. Construction materials based upon biologically renewable resources from components to finished parts. Polym Degrad Stab. 1998;59:251-61
  48. 48. Artamonova SV, Demina NM. New starch based textile onlining agent for glass fibres. Fibre chemistry 1997;29:68-70
  49. 49. Fang Q, Hanna MA. Preparation and Characterization of Biodegradable Copolyester–Starch Based Foams. Bio-resource Technology. 2001;78(2):115-22
  50. 50. Rhim JW, Ng PK. Natural biopolymer-based nanocomposite films for packaging applications. Critical Reviews in Food Science and Nutrition. 2007;47(4):411-33
  51. 51. Sekhon BS. Food nanotechnology - an overview. Nanotechnology, Science and Applications. 2010;3 1-15
  52. 52. Kaushik A, Arya SK, Vasudev A, Bhansali S. Recent Advances in Detection of Ochratoxin-A. Open Journal of Applied Biosensor. 2013;2:1-11
  53. 53. Zecheru T. Biopolymers for Military Use: Opportunities and Environment Implications - A Review. In: Elnashar M, editor. Biopolymers. Croatia: Sciyo; 2010. p. 597-612
  54. 54. Santos MI, Fuchs S, Gomes ME, Unger RE. Response of micro- and macrovascular endothelial cells to starch-based fiber meshes for bone tissue engineering. Biomaterials. 2007;28:240-8
  55. 55. Yoshimoto H, Shin YM, Terai H, Vacanti JP. A biodegradable nanofiber scaffold by electrospinning and its potential for bone tissue engineering. Biomaterials. 2003;24:2077-82
  56. 56. Purna SK, Babu M. Collagen based dressings- A review. Burn. 2000;26:54-62
  57. 57. Qurashi MT, Blair HS, Allen SJ. Studies on modified chitosan membranes. II.Dialysis of low molecular weight metabolites. Journal of Applied Polymer Science. 1992;46:263-9
  58. 58. Sparke BG, Murray DG. Chitosan based wound dressing materials. US Patent, 4572906. 1986
  59. 59. Hoekstra A, Struszczyk H, kivekas O. Percutaneous micro-crystalline chitosan application for sealing arterial puncture sites. Biomaterials. 1998;19:1467-71
  60. 60. WON CS. Vascular Tissue Engineering Scaffolds from Elastomeric Biodegradable Poly(L-lactide-co-ε-caprolactone) (PLCL) via Melt Spinning and Electrospinning. USA: North Carolina State University; 2006
  61. 61. Wang Q, Zhang N, Hu X, Yang J, Du Y. Chitosan/starch fibers and their properties for drug controlled release. European Journal of Pharmaceutics and Biopharmaceutics. 2007;66(3):398-404
  62. 62. Sun YM, Hsu SC, Lai JY. Transport properties of ionic drugs in the ammonio methacrylate copolymer membranes Journal of Pharmacy Research. 2001;18(3):304-10
  63. 63. SA] A, H Y, B O. Membrane formation by drycast process: model validation through morphological studies. Journal of Membrane Science 2005;249(1):63-72
  64. 64. Younes B, Ward SC, Christie RM, Vettese S. Textile applications of commercial photochromic dyes: part 7. A statistical investigation of the influence of photochromic dyes on the mechanical properties of thermoplastic fibres. The Journal of The Textile Institute. 2019;110(5):780-90
  65. 65. Ajeeb F, Younes B, Khsara AK. Investigating the Relationship between Thermochromic Pigment Based knitted Fabrics Properties and Human Body Temperature. IOSR J Polym Textile Eng. 2017;4(3):44-52
  66. 66. Younes B. Investigating the co-effect of twist and hot drawing processes on the bio-based yarns properties. The Journal of The Textile Institute. 2020;111(2):202-13
  67. 67. Basel Younes SCW, Robert M Christie. Textile applications of commercial photochromic dyes: part8. A statistical investigation of the influence of photochromic dyes on thermoplastic fibres. The Journal of The Textile Institute. 2019;under
  68. 68. Jena UCH, Elsner P. Biofunctional Textiles and the Skin. Basel (Switzerland): S. Karger; 2006
  69. 69. Younes B. Classification, characterization, and the production processes of biopolymers used in the textiles industry. The Journal of The Textile Institute. 2017;108(5):674-82
  70. 70. Aslan B, Ramaswamy S, Raina M, Gries T. Bio-composites : processing of thermoplastic biopolymers and industrial natural fibres from staple fibre blends up to fabric for composite applications. Journal of Textiles and Engineer. 1 9 9 2;19(85):47-51
  71. 71. Lim S, Lee J, Jang S, Lee S, Lee K, Choi H, et al. Synthetic Aliphatic Biodegradable Poly(butylene succinate)/Clay Nanocomposite Foams with High Blowing Ratio and Their Physical Characteristics. Polymer Engineering and Science. 2011;123:1316-25
  72. 72. Antipov EM, Dubinsky VA, Rebrov AV, Nekrasov YP, Gordeev SA, Ungar G. Strain-induced mesophase and hard-elastic behaviour of biodegradable polyhydroxyalkanoates fibers. Polymer. 2006 47:5678-90
  73. 73. Lim KY, Yoon KJ, Kim BC. Highly absorbable lyocell fiber spun from celluloses/hydrolyzed starch-g-PAN solution in NMMO monohydrate. European Polymer Journal 2003;39:2115-20
  74. 74. Lim KY, Yoon KJ, Kim BC. Highly absorbable lyocell fiber spun from celluloses/hydrolyzed starch-g-PAN solution in NMMO monohydrate. European Polymer Journal. 2003;39:2115-20
  75. 75. Strnad S, Šauperl O, Fras-Zemljič L. Cellulose Fibres Functionalised by Chitosan: Characterization and Application. In: Elnashar M, editor. Biopolymers. Croatia: Sciyo; 2010. p. 181-200
  76. 76. Czuryszkiewicz T, Ahvenlammi J, Kortesuo P, Ahola M, Kleitz F, Jokinen M, et al. Drug release from biodegradable silica fibers. Journal of Non-Crystalline Solids. 2002;306:1-10
  77. 77. Kopecek J, Yang J. Hydrogels as smart biomaterials. Polymer International. 2007;56(9):1078-98
  78. 78. Schmack G, Jehnichen D, Vogel R, Tandler B, Beyreuther R, Jacobsen S, et al. Biodegradable fibres spun from poly(lactide) generated by reactive extrusion. Journal of Biotechnology. 2001;86:151-60
  79. 79. Fletcher K. Sustainable Fashion and Textiles: Design Journeys. UK: Routledge; 2012
  80. 80. Bond EB, Autrn JPM, Mackey LN, Noda I, Odonnell HJ, inventorsWO 02/090630 A1, Multi-component fibres comprising starch and biodegradable polymer2002
  81. 81. Rong H, Bhat GS. Preparation and Properties Of Cotton-Eastar Nonwovens. International Nonwovens Journal. 2003;12(2):53-7
  82. 82. Bhat GS, Haoming R. Effect of Binder Fibres on Processing and Properties of Thermal Bonded Cotton-Based Non-woven. International Nonwovens Technical Conference, USA. 2002
  83. 83. Rong H, Leon RV, Bhat GS. Statistical Analysis of the Effect of Processing Conditions on the Strength of Thermal Point-Bonded Cotton-Based Nonwovens. Textile Research Journal. 2005;75(1):35-8
  84. 84. Bryan BE, Marie AJP, Neil ML, Isao N, Odonnell HJ, inventorsWO 02/090629 A1, Fibres comprising starch and biodegradable polymers2002
  85. 85. Bhat G, Kamath MG, Mueller D, Parikh DV, McLean M. Cotton-Based Composites for Automotive Applications. Global Plastics Environmental Conference, Michigan. 2004
  86. 86. Twarowska-Schmidt K, Ratajska M. Biodegradability of Non-Wovens Made of Aliphatic-Aromatic Polyester. FIBRES & TEXTILES in Eastern Europe. 2005;13(1):71-4
  87. 87. Twarowska-Schmidt K. Evaluation of the Suitability of Some Biodegradable Polymers for the Forming of Fibres. Fibres & Textiles in Eastern Europe. 2004;12(46):15-8
  88. 88. Mohanlal AP. Design and Study of Biodegradable Small Diameter Woven Vascular Grafts [Master Thesis]: North Carolina State University, USA; 2003
  89. 89. Kwon K, Kidoaki S, Matsuda T. Electrospun nano- to microfiber fabrics made of biodegradable copolyesters:structural characteristics, mechanical properties and cell adhesion potential. Biomaterials. 2005;26:3929-39
  90. 90. Kumar A, Srivastava A, Galaev IY, Mattiasson B. Smart polymers: Physical forms and bioengineering applications. Progress in Polymer Scence. 2007;32:1205-37
  91. 91. Lötzsch D, Ruhmann R, Seeboth A. Thermochromic Biopolymer Based on Natural Anthocyanidin Dyes Open Journal of Polymer Chemistry. 2013;3:43-7
  92. 92. Scott A. Spider Silk Poised For Commercial Entry. Chemical & Engineering 2014;92:24-7
  93. 93. Hult EL, Iotti M, Lenes M. Efficient Approach to High Barrier Packaging Using Microfibrillar Cellulose and Shellac. Cellulose, Springer. 2010;17:575-86
  94. 94. Knittel D, Buschmann HJ, Hipler C, Elsner P. Schollmeyer E: Funktionelle Textilien zur Hautpflege und als Therapeutikum. Akt Dermatol. 2004;30:11-7
  95. 95. Zemljič LF, Peršin Z, Stenius P, Stana-Kleinschek K. Carboxyl groups in pretreated regenerated cellulose fibres. Cellulose. 2008;15(5):681-90
  96. 96. hanmugasundaram WL. Development and characterization of cotton and organic cotton gauze fabric coated with biopolymers and antibiotic drugs for wound healing. Indian Journal of Fibre Textile Research 2012;37:146-50
  97. 97. Wang H-R, Chen K-M. Preparation and surface active properties of biodegradable dextrin derivative surfactants. Colloids and Surfaces A: Physicochem Eng Aspects. 2006;281:190-3
  98. 98. Mohanty AK, Khan MA, Hinrichsen G. Influence of chemical surface modification on the properties of biodegradable jute fabrics—polyester amide composites. Composites: Part A. 2000;31:143-50
  99. 99. Uretzkey G, Appelbaum AJ, Younes H. Long-term evaluation of a new selectively biodegradable vascular graft coated with polyethylene oxide-polylactic acid for right ventricle conduit. J Thorac Cardiovasc Surg. 1990;100:769-80
  100. 100. Madrigal-Carballoa S, Limb S, Rodrigueza G, Vilac AO, Kruegerb CG, Gunasekaranb S, et al. Biopolymer coating of soybean lecithin liposomes via layer-by-layer self-assembly as novel delivery system for ellagic acid. Journal of Functional Food. 2010;2:99-106
  101. 101. Pelton R. Temperature-sensitive aqueous microgels. Advances in Colloid and Interface Science. 2000;85(1):1-33
  102. 102. Lundin M. Adsorption of biopolymers and their layer-by-layer assemblies on hydrophilic surfaces [Doctoral Thesis]. Stockholm, Sweden: KTH Royal Institute of Technology; 2009
  103. 103. Jocić D, Tourrette A, Lavrič PK. Biopolymers: Biopolymer-Based Stimuli-Responsive Polymeric Systems for Functional Finishing of Textiles. Croatia: Sciyo; 2010
  104. 104. Lochner RH, Mater JE. Design for Quality. London Chapman and Hall; 1990
  105. 105. Clark KB, Wheelwright SC. The product development challenge: competing through speed, quality, and creativity. Boston: A Harvard business review book; 1995
  106. 106. Moreland JC, Sharp JL, Brown PJ. Lab-Scale Fiber Spinning Experimental Design Cost Comparison. Journal of Engineered Fibers and Fabrics. 2010;5(1):39-49
  107. 107. Ziabicki A, Jarecki L, Wasiak A. Dynamic modelling of melt spinning. Computational and Theoretical Polymer Science. 1998;8(1-2):143-57
  108. 108. Perera SSN. Viscoelastic Effect in the Non-Isothermal Melt Spinning Processes. Applied Mathematical Sciences. 2009;3(4):177-86
  109. 109. Wang GX, Matthys EF. Modelling of rapid solidification by meltspinning: effect of heat transfer in the cooling substrate. Materials Science and Engineering: A. 1991;136:85-97
  110. 110. Ziabicki A, Jarecki L, Wasiak A. Dynamic modelling of melt spinning. Computational and Theoretical Polymer Science. 1998;8(1/2):143-57
  111. 111. Kotze T. Two Dimensional Modelling of PET Melt Spinning: The effects of heat transfer limitations on the quality of PET yarn produced during melt spinning: LAP LAMBERT Academic Publishing; 2010
  112. 112. He W, Zhang S, Wang X. Mechanical Behavior of Irregular Fibers, Part I: Modeling the Tensile Behavior of Linear Elastic Fibers. Textile Research Journal. 2001;71(6):556-60
  113. 113. Bingol D, Tekin N, Alkan M. Brilliant Yellow dye adsorption onto sepiolite using a full factorial design. Applied Clay Science. 2010;50(3):315-21
  114. 114. Hanci TO, Alaton IA, Basar G. Multivariate analysis of anionic, cationic and nonionic textile surfactant degradation with the H 2 O 2 /UV-C process by using the capabilities of response surface methodology. Journal of Hazardous Materials. 2011;185,(1):193-203
  115. 115. Engin AB, Özdemir Ö, Turan M, Turan AZ. Color removal from textile dyebath effluents in a zeolite fixed bed reactor: Determination of optimum process conditions using Taguchi method. Journal of Hazardous Materials. 2008;159(2-3):348-53
  116. 116. Krucinska I. The influence of technological parameters on the filtration efficiency of electret needled non-woven fabrics. Article Journal of Electrostatics. 2002;56(2):143-53
  117. 117. Gardiner WP, Gettinby G. Experimental Design Techniques in Statistical Practice, A practical Software-Based Approach. Chichester, England: Horwood Publishing Limited; 1998
  118. 118. Tanguchi G. Introduction to Quality Engineering. Tokyo: Asian productivity organization; 1986
  119. 119. Younes B. The Statistical Modelling of Production Processes of Biodegradable Aliphatic Aromatic Co-Polyester Fibres used in the Textile Industry [PhD Thesis]. UK: Heriot-Watt University; 2012
  120. 120. Younes B. Simple Rheological Analysis Method of Spinnable-Polymer Flow Properties Using MFI Tester. Indian Journal of Materials Science. 2015(2015):1-8
  121. 121. Cawse JN. Experimental Design for Combinatorial and High Throughput Materials Development. USA: John Wiley and Sons, Inc; 2003
  122. 122. Younes B, Fotheringham A, Mather R. Statistical Modelling of the Effect of Multi-Stage Hot Drawing on the Thermal Shrinkage and Crystallographic Order of Biodegradable Aliphatic-Aromatic Co-Polyester Fibres. Fibers and Polymers. 2011;12(6):778-88
  123. 123. Younes B, Fotheringham A, Dessouky HME, Haddad G. The influence of multi-stage hot-drawing on the overall orientation of biodegradable aliphatic-aromatic co-polyester fibers. Journal of Engineered Fibers and Fabrics. 2013;8(1):6-16
  124. 124. Younes B. A Statistical Investigation of the Influence of the Multi-Stage Hot-Drawing Process on the Mechanical Properties of Biodegradable Linear Aliphatic-Aromatic Co-Polyester Fibers. Advances in Materials Science and Applications. 2014;3(4):186-202
  125. 125. Brody H. Synthetic fibre materials. London: Longman group UK limited 1994
  126. 126. Lord P. Hand Book of Yarn Production: Technology Science and Economics England: The Textile Institute & CRC & WP 2003
  127. 127. Tobler-Rohr MI. Handbook of Sustainable Textile Production. UK: Woodhead Publishing Limited; 2011
  128. 128. Callister W. Materials Science and Engineering: An Introduction. New York: John Wiley and Sons; 1999
  129. 129. Chen X. Modelling and predicting textile behaviour. UK: Woodhead Publishing Ltd; 2010

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Basel Younes

Submitted: 15 November 2020 Reviewed: 26 February 2021 Published: 30 March 2022