Relationship between nanoparticle size and nanoparticle toxicity [8].
\r\n\tof the any elected coordinates systems, bring the concept of a tensor. A tensor is a mathematical entity
\r\n\tborn of the invariance idea of the mentioned concepts in any election of coordinate systems and
\r\n\tto any coordinate system transformation. The concept has been of great importance to describe
\r\n\tthe invariance of the physics laws respect to any coordinate inertial reference frame where the physics
\r\n\tphenomena are measured. Likewise, the gravitation theory is an example of the importance of
\r\n\tdescribing the physics laws of the Universe through their invariants. Theories like general and special
\r\n\trelativity, bring the appearing of diverse Einstein summation laws and other properties used from
\r\n\tthe Levi-Civita calculus contributing to the appearing of the special tensors inside the Riemannian
\r\n\tstructure which best describes the Universe phenomena and their relations. Such is the case as the
\r\n\tRiemann tensors, the Pseudo-tensors and the different curvature tensors type arise from theories on
\r\n\tthe torsion field, the Cartan-Einstein theories or the supersymmetries in quantum mechanics.
\r\n\t
\r\n\tA focus more mathematical of the tensor is considering the multilinear forms and the tensor product of
\r\n\tthe vector spaces, where have more relevance to the applications the tensor product of Hilbert spaces,
\r\n\tfor example in QED and quantum mechanics. Applications in classical mechanics, electrodynamics,
\r\n\tquantum mechanics and communication theory are well developed through tensors,wherein quantum
\r\n\tcommunication theory and the parallel geometries to the Riemannian geometry, as twistor geometry
\r\n\tare considered the spinors and twistors as new re-interpretations of the tensors in fields and waves.
Nanotechnology is the study of materials, compounds, devices, and/or systems at near atomic or molecular levels [1]. Usually, one of the dimensions of nanoproducts is between 1 nm and 100 nm length in scale. This emerging technology involves fabricating, imaging, measuring, modeling, and manipulating matter at this scale [2]. The goal of nanotechnology is to control individual atoms, molecules, or particles in order to significantly improve the physical, chemical, physicochemical, and biological properties of materials and devices for various humanitarian purposes. One of the most important aspects of nanotechnology is the greatly improved surface area-to-volume ratio at this level. It includes a broad range of highly multidisciplinary fields, such as engineering, materials science, colloidal science, physics, chemistry, pharmacy, medicine, and biology [3].
\n\t\t\t\tNanomaterials can exhibit entirely different properties than their bulk-scaled conventional materials, enabling them to be appealing materials in many industrial applications [3]. For example, inert materials become catalytic materials (e.g., platinum and gold), opaque substances turn out to be transparent materials (e.g., carbon, copper), melting temperatures of solid materials are greatly reduced (e.g., gold, platinum, titanium), semiconductors become conductors (e.g., silicon, germanium), and non-combustible materials turn into combustible materials (e.g., aluminum) [1-3]. These fascinating behaviors of nanomaterials can be obtained only at nanoscale.
\n\t\t\t\tNanomaterials, including nanoparticles, nanotubes, nanofibers, and nanocomposites, in the forms of metals and alloys, ceramics, polymers, and composites are all produced by nanotechnology processes and are considered to be the next generation of materials for manufacturing faster cars and planes, more powerful computers and satellites, more sensitive sensors, stronger materials for structural applications, and better micro- and nanochips and batteries [1]. This is because nanomaterials have outstanding mechanical, electrical, optical, magnetic, quantum mechanic, and thermal properties. Nanomaterials are already found in more than a thousand different products, including bacteria-free cloth, concrete, filtration units, sunscreen, car bumpers, tooth paste, polymeric coatings, solar and fuel cells, lithium-ion batteries, tennis rackets, wrinkle-resistant clothing, and optical, electronic, and sensing devices [2]. In the near future, the use of nanomaterials will drastically increase worldwide. It is expected that the global market growth of nanotechnology is on track to reach one trillion dollars, and 50 percent of all new products will be nanotechnology-oriented by the year 2015 [20,21].
\n\t\t\tThroughout the manufacturing, transportation, storage, consumption, and waste disposal of nanomaterials, the air, water, soil, and food (e.g., vegetables, fruits, and animal products) can become contaminated, resulting in countless public concerns [8,22]. Nanoparticles can also remain airborne for hundreds of kilometers and penetrate humans, animals, and plant cells, causing many known and unknown side effects [4]. Nanomaterials mainly enter the human body by inhalation, ingestion, and/or contact through skin and persist in the system. Most human-made nanomaterials do not appear in the environment, so living organisms may not have an appropriate immune system to deal with these nanoscale products [5,8]. Recent studies show that when some nanomaterials of varying surface areas, sizes, shapes, charges and energy, and compounds interact with human and animal cells or organs, they can damage or kill those cells or organs, block blood flow, and cause serious diseases [6,7]. Illnesses associated with nanomaterials include bronchitis, asthma, lung and liver cancer, Parkinson’s disease, Alzheimer’s disease, Crohn’s disease, heart disease, and colon cancer [4,5]. Understanding the mechanisms and causes of nanomaterials will allow us to find efficient cures for lung diseases and other related illnesses associated with nanomaterials and devices [8,9].
\n\t\t\t\tSince nanomaterials are a new set of materials produced by entirely new manufacturing techniques, there are currently no specific rules and regulations for many of them. Hence, these uncertainties bring nanoethics and bioethics in research, development, and education to seek and examine the potential risks and rewards of the applications of these materials, as well as societal, economic, moral, health, and other broader human implications of advances in this technology [23-27].
\n\t\t\t\tObjectives of this study are as follows: i) to understand the surface properties of nanomaterials, ii) to determine the effects of nanoscale surfaces on the lung and other related diseases associated with nanomaterials, iii) to find possible protection methods for students, scientists, engineers, medical personnel, policymakers, and regulators working in the field, and iv) to inform these groups of people about progress and future developments in the field [4,]. Some of these objectives and future developments are summarized below.
\n\t\t\tSurface chemistry, surface potential, surface area, and particle size are dominating factors in the toxicity of nanomaterials [4-8]. These materials can react with the body, stay inert, and/or interact with a system based on their surface properties, and they can settle in the body for a long period of time [9-11]. It has been stated that almost all properties of nanoparticles are entirely different than their bulk-size counterparts [2]. Since the properties of nanomaterials are completely different, their toxicity could be different as well. Recent toxicological studies have demonstrated that particles less than 100 nm induce toxicity in many cell-cultured human and animal models [4-11]. Figure 1 shows the comparison of rat macrophage cells (raw cells) with different particles. As can be seen, nanoparticles are several orders of magnitude smaller than human and animal cells. They can be even smaller than DNA, pathogens, proteins, and enzymes [1]. Previous studies confirm that the smaller the particle size, the higher the toxicity [8,14]. Note that human macrophages are approximately twice as large as rat macrophages, so nanoparticle penetration may be easier for human macrophages or other larger living entities.
\n\t\t\tThe surface area of nanomaterials is exponentially high when the size is at nanoscale, so the surface chemistry (e.g., surface charge, zeta potential, and surface energy) of materials is drastically changed. The high surface area of nanomaterials means numerous unbonded atoms, resulting in huge surface interaction with surrounding tissues. Hence, surface chemistry can basically provide information about the mechanisms of biological toxicity of nanomaterials in cells [4,6]. For example, gold, silver, and platinum are chemically inactive and usually do not interact directly with the body at bulk scale. Allergic reactions and other toxic effects of these inert materials are at minimum level in bulk or at microscale. However, because of their size, the surface of nanoscale materials can be chemically activated to harm the surrounding cells or organs [4]. Some nanomaterials have higher surface-to-volume ratios, which can be also responsible for the shape-dependent surface reactivity and toxicity [12-17].
\n\t\t\tVarious images of cells and nanoparticles: A) rat raw cells (macrophages) at lower magnification, B) TEM image of magnetic nanoparticles with average diameter of 10 µm, C) comparison of raw macrophage cells, and D) drawings of particles at various size ranges.
Nanoparticles tend to aggregate due to intermolecular interactions, such as electrostatic, hydrophobic, and van der Waals, which makes the aggregation process easier [39]. Particle agglomeration, stability, and distribution can be related to surface charge and zeta potential values of nanoparticles in an aqueous media. The surface charge mainly regulates the stability of the nanoparticles [1]. At lower surface charges, nanoparticles usually agglomerate and make a larger cluster [2]. It has been reported that the toxicity of single particles is much higher than that of aggregated nanoparticles [4].
\n\t\t\tThe toxicity of nanomaterials can be minimized using different chemical processes, such as surface treatment, modification, and functionalization [39-42]. In this way, surface energy and surface charge of nanoparticles can be changed via additions of chemicals (e.g., surfactants, electrolytes, and polymers). These chemicals include (but are not limited to) citric acid, tetramethyl ammonium hydroxide, gum Arabic, sodium dodecyl sulfate, and other carboxyl and amine functionalization groups. As a result, the surface functionalization process will help nanomaterials perform at less toxic levels in the body or in other applications [6,7].
\n\t\tNanomaterials can enter the human body by various routes, such as breathing, eating, and touching the skin (Figure 2) [4-8,29,45]. Skin is the first defense barrier against the outside environment and is typically the first place on the body that is exposed to nanomaterial toxicity. Larger micron-scale particles normally cannot pass through skin and will not cause any health concerns. For the past few years, toxicological studies demonstrated that particles less than 100 nm in diameter induce toxicity in cell-cultured models as well as animal models [28-31]. It is also more difficult to remove nanoparticles from the body than the same kinds of larger particles. Table 1 shows the relationship between nanoparticle size and possible toxicity to living cells [8]. As is known, several kinds of sicknesses can be expected from nanomaterials that accumulate in the body, including inflammation of the airways, bronchitis, asthma, emphysema, lung cancer, neurodegenerative diseases, cardiovascular effects, liver cancer, Parkinson’s disease, Alzheimer’s disease, Crohn’s disease, heart disease, and colon cancer [4,40].
\n\t\t\tUnless functionalized, most nanomaterials are not stable in in-vitro conditions, so their stability is dependent on several factors, such as pH, ionic strength, solubility, thermodynamic feasibility, concentration, kinetic facility of electron transfers, and redox conditions of biological media [5]. The toxicity of nanomaterials can occur through three different mechanisms in the body: i) dissolution process of nanomaterials in biological media, ii) catalyst properties of nanomaterials, and iii) reduction and oxidation (Redox) evolution of the surfaces [4-6].
\n\t\t\tIn one study, an organ exposed to nanoparticles was analyzed, and the results indicated that the smaller particles diffused into the respiratory system faster than microscale particles [5]. It was also found that nanoparticles penetrate into cells and, by transcytosis, across epithelial and endothelial cells and into lymph circulation to reach very sensitive parts of the body, such as the nervous system, bone marrow, brain, lymph nodes, spleen, and heart. This study concluded that surface coating and in-vivo surface modification could reduce the side effects of those nanoparticles [6,7]. Figure 3 shows the nanoparticles of a lead compound and scanning transmission electrograph of ceria nanoparticles exposed to clearing sludge [29,45].
\n\t\t\tEntrances of nanoscale materials into the body through inhalation, dermal exposure, and ingestion, resulting in many potential hazards [25].
Lung disease involves many illnesses, such as bronchitis, asthma, chronic obstructive pulmonary disease, influenza, pneumonia, tuberculosis, cancer, and many other breathing-related illnesses [5]. Recent studies have shown that some lung diseases, such as bronchitis and asthma, are directly linked to the uptake of nanomaterials. After the inhalation of nanomaterials, they can be deposited throughout the entire respiratory system, beginning in the nose to the inside of the lung, which has airways that transport air combined with nanomaterials in (mostly) and out (rarely) of the body. Because of the larger surface area of lungs, nanoparticles have a primary entry route. Although larger particles (more than 10 µm) tend to be deposited in the upper part of the respiratory system and removed easily by the body through coughing and sneezing, smaller nanoscale particles can reach the gas exchange surfaces and remain there for a longer period of time. This is where the real problem begins [8].
\n\t\t\tBroken surfaces and other damage in the lung and other parts of the respiratory system accelerate the penetration of nanomaterials into the surrounding tissue, resulting in faster-growing lung diseases [4]. Also, when nanoparticles enter the blood stream, they can be
\n\t\t\t\n\t\t\t\t\t\t\tType of Material\n\t\t\t\t\t\t | \n\t\t\t\t\t\tParticle Size (nm) | \n\t\t\t\t\t\tSurface Area ( m2/g) | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\tCharge/Zeta Potential (mV)\n\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\tBiological Toxicity\n\t\t\t\t\t\t | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tAlumina\n\t\t\t\t\t\t | \n\t\t\t\t\t\t116 | \n\t\t\t\t\t\t13.37 | \n\t\t\t\t\t\t45-50 | \n\t\t\t\t\t\tProtein (BSA) adsorption with time | \n\t\t\t\t\t
\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | (pH 5.5–6.5) | \n\t\t\t\t\t\tIEP shifts with pH and surface area | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tPEG Quantum Dots\n\t\t\t\t\t\t | \n\t\t\t\t\t\t10 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tRetention of Q dots in liver, spleen, and bone marrow | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tMWCNT\n\t\t\t\t\t\t | \n\t\t\t\t\t\t10–20 | \n\t\t\t\t\t\t40–300 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tCytotoxicity: alveolar macrophages at high dose | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tSWCNT\n\t\t\t\t\t\t | \n\t\t\t\t\t\t1.4 | \n\t\t\t\t\t\t270 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tCytotoxicity: alveolar macrophages at low dose; | \n\t\t\t\t\t
\n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | \n\t\t\t\t\t\t | transient inflammatory and cell injury | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tTitania\n\t\t\t\t\t\t | \n\t\t\t\t\t\t300nm(rutile) | \n\t\t\t\t\t\t6 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tShort-term reversible inflammation | \n\t\t\t\t\t
\n\t\t\t\t\t\t | Rods(20–233) | \n\t\t\t\t\t\t26.5 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tShort-term reversible inflammation | \n\t\t\t\t\t
\n\t\t\t\t\t\t | (anatase rods) | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | — | \n\t\t\t\t\t\tMinor adverse lung tissue reaction | \n\t\t\t\t\t
\n\t\t\t\t\t\t | Spherical(5–6) | \n\t\t\t\t\t\t169.4 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tShort-term reversible inflammation | \n\t\t\t\t\t
\n\t\t\t\t\t\t | (anatase spherical powder) | \n\t\t\t\t\t\t\n\t\t\t\t\t\t | — | \n\t\t\t\t\t\tMinor adverse lung tissue reaction | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tQuartz\n\t\t\t\t\t\t | \n\t\t\t\t\t\t1.5µn | \n\t\t\t\t\t\t4 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tHigh pulmonary toxicity | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tPTFE\n\t\t\t\t\t\t | \n\t\t\t\t\t\t20 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tCell death–15 min. exposure | \n\t\t\t\t\t
\n\t\t\t\t\t\t | 130 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tNo ill effects | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tEmulsifying Wax\n\t\t\t\t\t\t | \n\t\t\t\t\t\t74.7 ± 53.4 (neutral) | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t–14.1 ± 2.1 | \n\t\t\t\t\t\tNo BBB; permeation ability in low conc. | \n\t\t\t\t\t
\n\t\t\t\t\t\t | 127.1 ± 70.6 (anionic) | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t–59 ± 2.9 | \n\t\t\t\t\t\tNo BBB; permeation ability in low concentrations | \n\t\t\t\t\t
\n\t\t\t\t\t\t | 97.2 ± 68.9 (cataionic) | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t45.2 ± 3.5 | \n\t\t\t\t\t\tToxic at brain microvasculaturue endothelium | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tCeria\n\t\t\t\t\t\t | \n\t\t\t\t\t\t3–5 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tRadio protection, nontoxic at low/medium dose | \n\t\t\t\t\t
\n\t\t\t\t\t\t\tYttria\n\t\t\t\t\t\t | \n\t\t\t\t\t\t50 | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\t— | \n\t\t\t\t\t\tNeuroprotection against oxidative stress | \n\t\t\t\t\t
Relationship between nanoparticle size and nanoparticle toxicity [8].
delivered to organs and tissues in the entire body, including the brain, heart, liver, kidneys, spleen, bone marrow, and nervous system [40]. Unlike larger particles, nanoparticles can reach the cell mitochondria and cell nuclei of these organs, which in turn cause DNA mutation and induce major structural damage and cell death [25,28,41]. In this case, particle size and shape are the major factors in determining particle toxicity.
\n\t\t\tNanoparticles of lead compound located in lung where patient was affected by multiorgan granulomatosis (left), and scanning transmission electrograph of ceria nanoparticles exposed to clearing sludge (high-density cerium oxide nanoparticles are bright) (right) [29,45].
One latest study showed that, after 12 weeks of inhalation tests, small TiO2 nanoparticles 20 nm in size were characterized by a longer retention time in the lungs of rats and increased translocation to interstitial sites than larger TiO2 nanoparticles 250 nm in size [4,50-52]. Another study in healthy animals also showed that inhalation of metallic nanoparticles (less than 30 nm) into the circulatory system was much faster than that of non-metallic nanoparticles (between 4 nm and 200 nm) [53]. Although the mechanism of nanomaterial penetration is not fully understood, it is believed that nanoparticles can be absorbed by lung cells and induce local effects, leading to long-term consequences of airway inflammation, bronchitis, asthma, emphysema, lung cancer, neurodegenerative diseases, and cardiovascular effects [4-6].
\n\t\t\tCarbon-based nanomaterials (CBNs) in different forms of fullerenes, single- and multi-walled carbon nanotubes (SWCNTs and MWCNTs), and carbon nanoparticles and nanofibers are being used in a number of different applications [1-3]. The shape of CBNs is an important factor in determining its toxicity [42]. Some CBNs are structurally similar to asbestos, raising concerns that widespread use of carbon nanotubes may lead to mesothelioma, cancer of the lining of the lungs caused by an exposure to asbestos. In particular, the needle-like fiber shapes of CNTs are more toxic than other CBNs are to human skin fibroblasts [46-49]. MWCNTs and SWCNTs have strong chemical stability, and when inhaled, they cannot be easily dissolved in the body, which in turn could damage cells, DNA, and surrounding tissues [42-44]. Generally, SWCNTs are more toxic than MWCNTs because of their size [6]. Recent studies have also shown that sidewall-functionalized MWCNTs and SWCNTs were less toxic to human cells than those without functionalization. Also, it is interesting to note that CNTs synthesized by a catalytic chemical vapor deposition are not toxic to human umbilical vein endothelial cells [4,32-34].
\n\t\t\tAlthough nanomaterials have superior properties in various applications, they can be very dangerous if not properly handled. Toxicity of nanomaterials has not been completely identified yet, and most studies have mainly focused on acute and liver toxicity [4,49]. Long-term toxicity of nanomaterials and examination of chronic exposure must be studied in detail to understand the mechanisms involved. Even though several factors are involved in nanomaterial toxicity, more efforts and time are needed to conduct research on nanoscale products and lung and other diseases [6,50].
\n\t\tHazard reduction of nanomaterials is necessary for students, engineers, and health professionals working on their production, processing, and analysis, as well as workers and consumers in contact with commercial products [5,35,36]. Table 2 provides a hierarchy of the exposure controls of nanomaterials at different categories, such as elimination, substitution, engineering, administration, and personal protective equipment [9,37].
\n\t\t\t\n\t\t\t\t\t\t\tControl Methods\n\t\t\t\t\t\t | \n\t\t\t\t\t\t\n\t\t\t\t\t\t\tProcess, Equipment, and Tasks\n\t\t\t\t\t\t | \n\t\t\t\t\t
Elimination | \n\t\t\t\t\t\tChange design to eliminate or minimize hazardous materials. | \n\t\t\t\t\t
Substitution | \n\t\t\t\t\t\tReplace high-hazard material with a low one (e.g., environmental). | \n\t\t\t\t\t
Engineering | \n\t\t\t\t\t\tUse isolation/enclosure, ventilation, filtration, and collection. | \n\t\t\t\t\t
Administration | \n\t\t\t\t\t\tAdhere to procedures, policies, shift design, and new rules and regulations. | \n\t\t\t\t\t
Personal Protective Equipment | \n\t\t\t\t\t\tUse respirators, clothing, gloves, goggles, and ear plugs. | \n\t\t\t\t\t
The processing, equipment, and job tasks associated with the control methods are as follows: i) change the design to eliminate or minimize hazardous materials; ii) replace a high-hazard material with a low one; iii) use isolation, ventilation, filtration, and dust collection; iv) adhere to procedures, policies, shift design, and new rules and regulations; and v) use respirators, clothing, gloves, goggles, and ear plugs. Figure 4 shows some methods of protection that should be used during the production and use of nanomaterials [5,35], which are outlined as follows [4-6]:
\n\t\t\tStudents, workers, engineers, doctors, and scientist who are working with nanomaterials and devices are recommended to wear a disposable, typically plastic, body covering over their work clothes during high-exposure activities and to wear long gloves pulled over their sleeves to minimize wrist exposure and other contamination. Other recommendations are antistatic shoes to prevent ignition by static charges, and sticky mats at laboratory entrances to prevent the accidental transfer of nanomaterials in and out of the working area [5].
The hazardous effects of nanomaterials need to be reduced during their production and processing. The waste of nanomaterials should be limited. Outputs are sometimes more hazardous than the products or wastes from such activities [5].
Workers who inhale nanomaterials are advised to consume milk and unrefined sugar to reduce the toxicity level of nanomaterials [5].
Nitrile gloves or wrist-length disposable nitrile gloves with extended sleeves must be worn during the handling of nanomaterials (Figure 4). These gloves need to be changed frequently[5].
For eye protection, safety glasses with side shields must be on the face during the use of nanomaterials in the form of solids, liquids, and aerosols [5].
Volumes of liquid-based nanomaterials must be limited to the milliliter range (< 200 ml) in a sealed container when not in use [5].
Total particle masses must be limited to the milligram range (< 200 mg) and must be manipulated within a high efficient particulate air (HEPA)-filtered laboratory exhaust hood over water-soaked absorbent paper to capture any spilled materials [5].
Containers of nanomaterials must be labeled with a sign indicating “NANOMATERIALS” [5].
Nanomaterials are considered to be hazardous materials, so workers should follow all the safety rules necessary in the field and laboratory [5].
The use of nanomaterials increasing worldwide brings with it several concerns for worker and user safety. Thus, new measurement devices should be developed and used in the specified areas where nanomaterials and devices are produced and utilized.
In addition to the previous information, the National Institute for Occupational Safety and Health (NIOSH) has provided sequential steps for students, workers, engineers, and others who are involved in nanotechnology-related teaching, research, and development [5,38]. These steps, shown in Figure 5, will potentially reduce the risk of exposing nanomaterials to personnel and consumers [5,38].
\n\t\t\tSimple protection methods for using potentially hazardous engineered nanomaterials in laboratory conditions.
Steps of NIOSH for workers/students involved in nanotechnology processes [5].
Although nanomaterials have superior properties for various applications, these materials could be more hazardous to human than their microscale equivalent if not properly handled or used. The nanomaterials mainly exposed through inhalation of suspended nanoscale particulates result in the inflammation of airways, bronchitis, asthma, emphysema, lung cancer, neurodegenerative diseases, and cardiovascular effects. Toxicity of nanomaterials has not been completely identified yet, and most studies have focused primarily on acute liver toxicity. The long-term toxicity of nanomaterials and examination of chronic exposure to these materials must be studied in detail to understand their toxicology mechanisms in the lungs and other organs. Even though several factors are involved in the toxicity of nanomaterials, more efforts and time are needed to study nanoproducts, their properties, and processing. Thus, students, scientists, engineers, doctors, policymakers, and regulators working in the field should take all the necessary precautions to protect themselves during the production, handling, and consumption of nanomaterials.
\n\t\tThe author gratefully acknowledges Wichita State University for the support of this work.
\n\t\tWater is an essential element for living systems. It facilitates the transport of nutrients and waste products within the body of living creatures [1]. Surface water is one of the important supplies for drinking water production [2]. Recently, surface water has been increasingly contaminated by microorganisms, organic matter, particles, and solids due to the developing effects of human activities and climate change as is depicted in Figure 1 [3, 4, 5]. This increase in the concentration of surface water contaminants has led to the increase in the cost associated with the treatment of water. The quality of the produced water has also deteriorated as a result of increased contamination. According to the World Health Organization (WHO), 5 million death cases per year worldwide are caused by poor quality drinking water [6]. These problems have made the enhancement of surface water treatment to cope with the increasing levels of contamination, an ultimate goal for the current research activities.
\nSources of surface water contamination.
Technically, the performance of surface water treatment systems depends on the efficiency of individual treatment processes in removing contaminants. Conventional surface water treatment systems consist of coagulation/flocculation, filtration, and disinfection [1]. A number of operational and health problems arise in the surface water treatment process as a result of increasing contamination. The most common problems are high level of dangerous residual metal coagulants such as aluminum (Al) [7], fouling of filtration media [8], and the formation of hazardous disinfection by-products (DBPs) [9].
\nResidual metals can cause operational and health problems. Increasing the Al concentration in water increases turbidity, causes filtration fouling, and interferes with disinfectants [10, 11, 12]. In addition to the technical problems, the residual Al in treated water can cause neuropathologic disorders, neurological diseases (e.g., Alzheimer’s and presenile dementia), and kidney diseases [10, 13].
\nFouling of filtration/adsorption media is another challenge that is commonly encountered in potable water treatment processes. Fouling can occur as a result of the deposition of various foulants, such as solid particles, organic contaminants, inorganic contaminants, and microorganisms, onto various filter surfaces [14]. Fouling of filters results in extra cost and delay on the filtration process as well as reducing the quality of the water produced [15]. The deeply embedded microorganisms in filtration media do not only act as a hidden source of pathogens but also release toxic metabolic products into water treatment systems [16].
\nThe formation of DBPs is a result disinfectants (e.g., chlorine and ozone) reaction with the organic matter [17, 18]. DBPs include a wide spectrum of carcinogenic and mutagenic chemical complexes that pose a threat to both humans and the environment. The two most prevalent classes of DBPs in drinking water are trihalomethanes (THMs) and haloacetic acids (HAAs) [19]. Total THMs (TTHMs) is the sum of four compounds: chloroform, bromodichloromethane, dibromochloromethane, and bromoform [20]. HAAs include nine compounds which encompass derivatives of HAAs (i.e., mono-, di-, and trihaloacetic acid) and iodine and bromine containing HAAs [19]. The most common HAAs are di- and trihaloacetic acid. Epidemiological and toxicological studies indicated that the human exposure to chlorinated water containing DBPs may lead to bladder cancer [21], deterioration in liver functionalities, kidney and nervous system [22], and congenital diseases [17]. Therefore, a maximum contamination level (MCL) of DBPs has been set for different countries around the world. For instance, the MCL of THMs in Australia is 250 μg L−1, while the MCL of monochloroacetic acid (MCAA), dichloroacetic acid (DCAA), and trichloroacetic acid (TCAA) are 150, 100, and 100 μg L−1, respectively [22, 23].
\nResearch efforts have been directed toward minimizing the challenges encountered in surface water treatment systems. It is obvious that the increasing levels of contamination and the conventional chemicals used for treatment are the main reasons behind these challenges. Hence, the quantities of chemicals added to water should be minimized without compromising the quality of the treated water. To this end, chemical-free (henceforth referred to as physical) treatment methods are recommended to be applied in surface water treatment schemes. It should be mentioned here that this study focuses on organic and microbial contamination; hence, the discussion in the following sections will be confined to aspects pertaining to the removal of such contaminants.
\nThe common physical treatment methods include pulsed-electric field and plasma discharge [24, 25], magnetic field [26], hydrodynamic cavitation [27], ultraviolet (UV) light [28], and ultrasound [29]. The combinations of physical-physical treatments such as UV light and ultrasound and physical-chemical treatments such as ultrasound and chlorine dioxide, ultrasound and ozone, and UV and ozone are also recommended [30].
\nThe organic contamination of natural surface water is represented by the existence of natural organic matter (NOM) in water sources. NOM can be categorized based on size into particulate organic carbon (POC) and dissolved organic carbon (DOC). NOM fraction that passes through 0.45 μm filter is termed as DOC, while the retained fraction is termed as POC. The latter only forms 10% of NOM and can easily be removed from water [31]. Therefore, attention should be given to improving DOC removal from natural water.
\nDOC encompasses a vast array of organic materials that varies in their characteristics spatiotemporally [32]. DOC can be classified into groups based on origin and structure. Origin-based classification categorizes DOC into three groups: allochthonous, autochthonous, and anthropogenic [33]. Allochthonous is derived from natural decomposition of soil and plants, while autochthonous DOC is originated from algal and microbial activities. The anthropogenic DOC in surface water is emanated from human activities and wastewater treatment processes [33]. Potable water sources contain mainly allochthonous and autochthonous carbon [34]. The concentration of autochthonous DOC in surface water depends strongly on the hydraulic residence time of water in reservoirs and this would naturally reduce its contribution to overall organic contamination. Hence, improving allochthonous DOC removal would be of more importance to drinking water treatment practices.
\nThe structural classification mainly divides DOC into hydrophobic and hydrophilic fractions [35]. The proportion of these fractions in natural water catchments depends on the carbon source and other factors such as microbial activities and natural photo-degradation. The hydrophobic fraction is comprised mainly of humic and fulvic acids, phenolic DOC, and double bond structures [36]. The hydrophilic fraction mainly contains aliphatic and nitrogenous compounds [35]. DOC structure is important from water treatment perspective as these fractions are associated with certain health and operational problems [37]. For instance, hydrophobic DOC is known to have a tendency to react with chlorine forming DBPs [38].
\nThe main DOC removal mechanisms of physical treatments are (i) chemical reactions (e.g., radicals attack), (ii) physical effects (e.g., shear forces, pyrolysis), and (iii) alteration of physical properties (absorptivity). A wide range of radicals are produced when exposing water to physical treatments such UV and ultrasound. The most important radical species is the hydroxyl (•OH) as it possesses a high oxidation potential (2.8 V) that exceeds the oxidation potentials of common oxidants such as atomic oxygen (2.42 V), ozone (2.07 V), and hydrogen peroxide (1.78 V) [39]. The •OH pathway reactions with NOM include addition to double bonds and hydrogen and electron abstraction [35]. Chemical mechanisms are prominent in electrical and UV techniques, while the combination of both chemical and physical mechanisms is generated with techniques such as ultrasound and hydrodynamic cavitation [40]. Physical treatments that utilize magnetic fields can alter physical properties of DOC, making it more susceptible to removal via adsorption [6, 26]. It is worth mentioning that physical methods that produce •OH are also capable of altering the nature of remnant DOC [41].
\nGenerally, DOC removal levels are low with the physical treatments as stand-alone technologies; however, combining these methods with chemicals addition can significantly boost DOC removal [35]. Chemical addition to some treatment methods such as UV and electrical methods can be problematic. For instance, the addition of TiO2 in photo-catalysis (UV/semi-conductors) requires an additional treatment to remove TiO2 particles from the treated water, and this in turn introduces extra cost [42]. The addition of electrolytes such as NaCl [35], or KCl [43] in electrochemical oxidation can also cause some technical problems such as the conformational change of DOC [44] resulting in a compact fouling layer. Electrodes and UV lamps are also prone to fouling problems that require frequent maintenance [45]. Furthermore, the use of UV method, particularly vacuum UV (VUV), was found to produce undesired nitrite by-products [35]. Similarly, magnetic field technique can potentially cause some health problems. It was reported that the use of magnetically treated water negatively affects the functionality of rats’ kidneys suggesting that magnetic treatment can cause unstable changes to bio-mechanisms of tissue fluid [46]. Generally, electrical, magnetic, and UV treatments require mixing to ensure uniform effective treatments which adds to energy requirements of these techniques. By way of contrast, mixing is not required for dynamic treatments such as ultrasound and hydrodynamic cavitation. These treatments were also found to have benign environmental effects [47]. However, hydrodynamic cavitation has some disadvantages such as the unclear effect of operating parameters on cavitation events [48], the requirement of long treatment time to achieve perceptible change, and mechanical erosion of equipment [47]. The main disadvantage of ultrasound is high operational energy demand [49], nevertheless the installation and maintenance cost is low due to its simple configuration [50]. Recent studies have reported that ultrasound is more energy efficient compared to hydrodynamic cavitation and UV in removing organic materials [25].
\nVarious species of microbes are present in surface water. However, microbial contamination of water is normally evaluated through indicators such as total coliform and E. coli [51]. The mechanisms of microbial removal/inactivation using physical treatment methods are similar to those of NOM removal. The produced highly oxidative agents attach the structure of microbes weakening their resistance to the surrounding environmental conditions. Similar microbial structural damage can be induced by the strong mechanical effects such as powerful turbulences and shockwaves. Generally, UV and electrical disinfection techniques rely on chemical effects; with ultrasound and hydrodynamic cavitation, the mechanical effects have a more prominent role as opposed to thermal and chemical effects [52].
\nAs far as the performance is concerned, UV and electrical techniques have the disadvantages of producing mutagenic activities and low performance with turbid water [14, 53]. Hydrodynamic cavitation has some shortcomings as mentioned in Section 2.1.3. In contrast, ultrasound technology has advantages of being environmentally friendly and easy to implement and control, which outweighs the disadvantage of high energy demand. Even the high energy demand reputation for ultrasound technology may be attributed to the inefficient utilization of energy in this technology which will be discussed further in the coming sections.
\nGiven the potential of ultrasound technology in solving the emerging problems in drinking water treatment process, this chapter will provide critical review on this matter.
\nUltrasound is a longitudinal wave with frequency ranges between 16 kHz and 500 MHz [54]. The propagation of ultrasound waves through water produces alternating cycles of positive and negative pressure. When the magnitude of the ultrasonic pressure exceeds the tensile strength of the liquid, cavitational bubbles are created. The formed cavitational bubbles and existing gas bubbles in the liquid grow to a size larger than their original size during the negative cycle of the ultrasonic pressure. Some bubbles grow to a very large size due to gas transfer across bubble skin (rectified diffusion) or coalescence with other bubbles, and eventually float to water surface. Other bubbles collapse during the positive cycle of the ultrasonic wave. In terms of collapse intensity, there are two kinds of bubbles; bubbles with gentle collapse “stable bubbles” and bubbles with severe collapse “transit bubbles” [55]. There are two sources for bubbles generated in ultrasonically excited water: dissolved gas and gas entrapped in crevices of solid surfaces. The formation of bubbles from dissolved gas is normally termed as homogeneous cavitation, while bubbles formation on liquid-solid interface is termed as heterogeneous cavitation [56].
\nThe physics and chemistry of transit bubbles are of interest from water treatment perspective owing to the powerful effects produced from such bubbles collapse. These effects are represented by the generation of localized areas of high temperature and pressure of around 5000 K and 500 atm, respectively, usually referred to as hot spots [40]. There is a variation in the temperature profile within the localized areas of hot spots which determines the nature of reactions occurring in each area. The three recognized zones of the hot spots are [40, 57]:
Thermolytic center represents the center of the cavitational bubble. During bubble collapse, the temperature and the pressure of this zone reach approximately 5000 K and 500 atm, respectively. The materials phase in this region is gaseous, so it can be inferred that the high temperatures in this region can lead to the thermolysis of the volatile DOC and water vapor exist in the region [58]. The thermolysis of water vapor produces free radicals that can further decompose volatile DOC.
Interfacial zone is present between bubble skin and the bulk solution. The thickness of this region is around 200 nm, and the life time of this region is about 2 μs [57]. The temperature in this region reaches to approximately 2000 K at the final collapse of the bubble [59]. The material phase in this region is a supercritical fluid. The high temperature in the interfacial zone facilitates the thermolysis and the oxidation of nonvolatile DOC.
Bulk solution region: the pressure in this region is equal to the ambient pressure; whereas, the temperature is variable depending on ultrasound operating parameters. The hydroxyl radicals recombine in the bulk solution region producing hydrogen peroxide, which in turn can oxidize nonvolatile DOC.
Bubble’s oscillation and collapse generate acoustic streaming, microstreaming, microjetting, turbulence, shock wave, and shear stress [60]. Acoustic streaming is defined as the convective liquid motion due to the passage of ultrasound waves. Microstreaming is the liquid motion in the adjacent area to oscillating bubbles. Microjetting is the resulting liquid motion from bubble symmetrical collapse close to the solid/liquid interface [61]. The physical and chemical effects of ultrasound can be harnessed for organic and microbial contamination removal.
\nFigure 2 illustrates the physical and chemical effects of ultrasound on water contaminants. The physical effects such as the powerful turbulences and shock waves can disintegrate organic and microbial structures, as reported by several studies [49, 60].
\nMechanisms of acoustic cavitation in degrading water pollutants.
Chemical effects of ultrasound are evident through the liberation of highly reactive species that have the capacity to cleave chemical bonds. The reactive species are short lived intermediates [62]; therefore, their effect is expected to occur only during the short time of the bubble’s collapse. As explained earlier, volatile compounds are likely to decompose in the thermolytic center due to the effects of free radicals.
\nThe nonvolatile compounds in water are divided into two groups: hydrophobic and hydrophilic compounds. The repulsive nature of hydrophobic compounds to water forces these compounds to accumulate in the area adjacent to collapsing bubbles, which in turn facilitates the ultrasonic-induced chemical decomposition of these compounds by free radicals, as demonstrated in Figure 2. The case is different for nonvolatile hydrophilic compounds, as the concentration of such compounds in the sheath around the bubble is similar to that in the bulk solution region. So the hydrophilic compounds are either chemically disintegrated by free radicals and their recombination products or mechanically destructed via the mechanical shear and shock waves resulting from bubble oscillations and collapse [63]. The shear stresses’ and shock waves’ degradation of organic materials is attributed to the slight phase difference, especially for humic polymeric structures. Many researchers have reported the capacity of shear stresses and shockwaves on breaking the chain structure of polymeric organic materials or opening the ring structure of cyclic organic materials [57]. Additionally, the extreme conditions in the collapsing bubble’s center and the surrounding areas can lead to the formation of acids [64], which can reduce the solubility of humic acid and consequently increases its degradation by the physical effects.
\nAlthough inorganic contaminants are outside the scope of this study, it is worth mentioning that microstreaming and generated oxidative species instigated by bubble collapse are the main ultrasonic removal mechanisms for these contaminants [65].
\nUltrasound waves are commonly generated by converting electrical power into vibration using transducers. There are two types of transducers: piezoelectric and magnetostrictive [66]. A graphical representation of these transducers is shown in Figure 3. For piezoelectric transducers, the vibration is created via exciting the piezoelectric crystal with electrical current, as demonstrated in Figure 3a. In the case of magnetostrictive transducers, the electrical current is passed through coils inducing a magnetic field that causes contraction and expansion of the ferromagnetic core (Terfenol-D of Nickel in most cases), as shown in Figure 3b. Comprehensive comparison between the characteristics of magnetostrictive and piezoelectric transducers is provided in [67]. Although the performance of magnetostrictive transducers outstrips that of piezoelectric transducers [68, 69], there is limited number of studies concerning the use of these transducers for water treatment applications.
\nCommon ultrasonic wave generation techniques: (a) piezoelectric and (b) magnetostrictive.
Ultrasound irradiation can be applied in two modes: continuous and pulsed. Continuous mode is more commonly used for water treatment application compared to the pulsed mode. In pulsed mode, the operation is interrupted for a preset amount of time. The period during which ultrasound operates is known as pulse; whereas, the interruption time is normally termed as interval. The pulse and interval are denoted, respectively, as On and Off periods. The On:Off ratio is commonly denoted as R. Operating ultrasound in a pulsed mode is more energy-efficient due to minimizing bubble’s cloud size that occurs near the irradiating surface especially at high-power levels (reduction of shielding effects) [57]. During the Off period, the ineffective cloud bubbles dissolve and/or float to the surface leaving less number of ineffective bubbles close to the irradiating surface, which means less energy is absorbed/scattered by bubbles [70], as illustrated in Figure 4. Other positive aspects of applying pulsed mode ultrasound include improvement of pollutants transport to reaction sites of collapsing bubbles, spatial enlargement of the active zone, and utilization of acoustic residual energy during the Off period. Operating ultrasound in pulsed mode also reduces temperature rise that can be undesirable for some water treatment applications such as filtration [14].
\nIllustration of pulsed mode alleviation of shielding effects.
Operating ultrasound in pulsed mode does not always result in improved performance [71]; it depends on applying a suitable power level for the chosen R ratio. Hence, optimizing pulse ratios and power levels are of utmost importance for pulsed ultrasound applications. Using pulsed ultrasound for water contaminants removal was investigated by a limited number of studies, such as the studies conducted by [72, 73]. These studies dealt only with synthetic water samples. Recent studies proved the capability of pulsed ultrasound in removing natural water contaminants [74].
\nLike other treatment technologies, the performance of ultrasound is influenced by several factors. These factors can be broken down into three groups: system operating conditions, medium characteristics, and design-related aspects. The operating parameters of ultrasonic equipment include power, frequency, treatment time, mode of operation, and shape of the exciting waves (i.e., sine, triangle, etc.). It is known that increasing the power results in more intense ultrasonic effects; however, power impact normally follows a logarithmic growth trend, where increasing beyond a certain limit can only results in little improvement. Frequency has a direct relationship with cavitation threshold; therefore, the higher the frequency, the more the power required to generate cavitation bubbles [75]. As discussed in the previous section, pulsed mode is more energy-efficient than the continuous mode. Among the common exciting waves’ shapes, square wave has the highest ultrasonic effects [67].
\nMedium characteristics such as viscosity, pressure, temperature, and contents of solid and gas impurities can affect the intensity of ultrasound effects. Viscosity has a negative effect on the generation and collapse of cavitating bubbles. It is difficult for ultrasonic waves to propagate through a viscous medium due to high cohesion forces; hence, less effective acoustic events would be achieved [76]. In the case of typical surface water treatment system, change in water viscosity is not expected to occur, and hence the effect of this factor can be ignored. The effect of the ambient pressure on ultrasound comes into play only when dealing with closed system treatment chambers. Increasing the ambient pressure has two conflicting effects: decreases the vapor content in the collapsing bubble leading to more effective bubble collapse [54] and at the same time negatively affects bubble growth leading to less violent collapse [77]. The ambient temperature impacts ultrasound performance in a similar fashion. Increasing the temperature facilitates bubbles formation due to reduction in medium viscosity; however, the vapor content in the formed bubbles would be high leading to a less violent collapse (cushioning effects) [77]. It should be mentioned that increasing the ambient temperature can accelerate both microbial disruption and chemical reactions under the effect of ultrasound [54, 77]. This means that the net temperature effect on ultrasound performance is positive.
\nThe impact of solid particles and dissolved gas bubbles depends on their nature and the treatment purpose. Bubbles formed from gases with high specific heat ratio produce better cavitation effects (higher temperature and larger number of radicals) compared to those generated from gases with low specific heat ratio [78]. The presence of solid particles in water can be beneficial if the treatment is targeting microbes’ removal [79, 80], or adverse if the treatment goal is DOC removal [81]. In the case of surface water treatment, the dissolved gas would mostly be air resulting in relatively high acoustic effects compared to other gases such as O2 and Ar [82]. The presence of solids in surface water is inevitable, and they would be a mixture of soil aggregates that release DOC upon ultrasound exposure [81] and solid particles that promote heterogeneous cavitation [80].
\nThe aspects of ultrasonic reactor design such as reactor shape and liquid height play crucial roles in the homogeneity of acoustic energy distribution and the uniformity of treatment across the treated volume. Generally, reactors with curvatures (e.g., conical or cylindrical) are more effective in utilizing ultrasound power compared to the standard rectangular-shaped reactors [83, 84]. This is attributed to the reflection of the waves back from the curved walls to the water in different directions resulting in more acoustic events. However, reactors with flat surfaces are easier to design and modify to accommodate monitoring and measurements equipment [57]. An example of such a design is the hexagonal reactor proposed by Gogate et al. [85], where waves can still be reflected from the walls. The liquid height has a negative effect on ultrasound performance; the further away the contaminants are from ultrasonic source, the less effective the treatment is [57]. Interestingly though, in a study conducted by Asakura et al. [86] on the effect of liquid height on ultrasound chemical activity at different frequencies showed that at largest height investigated (500 mm), low frequency ultrasound resulted in the highest chemical throughput compared to other tested frequencies (>100 kHz). In the same manner, Sharma and Sanghi [87] reported that low frequency results in better distribution of acoustic energy in large-scale volumes. This suggests that low frequency ultrasound operation has the potential to be successfully scaled up to industrial levels.
\nThe scalability of ultrasound technology for drinking water treatment purposes requires multi-disciplinary expertise such as chemistry, electrical engineering, chemical engineering, material sciences, etc. One essential step toward scalability is applying an accurate energy characterization technique. The use of an inappropriate characterization method would produce discouraging energy figures that would be disincentive for industries interested in adopting ultrasound technology.
\nThere are many techniques for determining the capacity of ultrasound equipment in converting electrical power to useful acoustic energy. Among all the reported energy characterization techniques, calorimetric technique is the most commonly used owing to its simplicity and cost-effectiveness [88]. However, this technique must be carefully applied. The use of a single location for temperature measurements as being representative for the whole irradiated volume is not appropriate, especially for low power levels where standing wave effects are evident [89]. The other aspect that needs to be carefully considered is the heat loss via convection during the time of temperature recording. Convective heat loss would be more noticeable in the cases of high-power application and pulsed operation. At high ultrasonic power, the temperature rise is rapid which would accelerate thermal energy dissipation through the walls of the containing vessel to the atmosphere. In the case of pulsed ultrasound, long irradiation time is required to obtain tangible temperature rise and this would allow enough time for the generated heat to escape to the atmosphere. This explains why some studies have reported efficiency as low as 30% for ultrasonic horn [90], while others reported efficiency as high as 60–70% [91] for the same reactor type, as the latter used a sophisticated adiabatic reaction vessel that prevents convective heat loss.
\nMany scale-up attempts of ultrasonic reactors were reported in the literature [92]. The prominent approaches were: multistage reactors [49], flow-cells [93], sonitube [89], super-positioning multiple transducers of similar or different frequencies [57], and the use of reflectors [94, 95]. The approach of combined multi-transducers and reflectors seems to be a promising strategy for ultrasonic reactor scale-up as the interaction of waves emitted from transducers and the reflected waves from reflectors would enlarge the active zone in the reactor. However, it is worth mentioning that most of these scale-up attempts utilized the commercially available piezoelectric transducers that operate largely on sine wave excitation. Recent studies have shown that some waveforms other than the sine wave can result in better excitation of transducers [96]. Thus, exploring the use of other transducer types and waveforms in large-scale applications is imperative to provide broader and may be more efficient options to industry.
\nThe common use of ultrasound in coagulation process is as a pre-treatment for the process to improve blue-green algae removal [97]. The presence of blue-green algae in the water treatment system has been associated with many problems such as clogging membrane pores, undesirable taste and odor, production of DBPs, and the release of toxic compounds such as Microcystin [98]. Ultrasonic mechanism for algae removal is ascribed to the destruction of gas vacuoles that are responsible of algae buoyancy [97]. There is also a recent study that has utilized ultrasound as a mean of mixing for algae removal using chitosan [99]. Removing algae requires applying low frequency, moderate input power, and short treatment time.
\nThe application of low power ultrasound for a short treatment time in algae removal applications can solve the seasonal problem of algal bloom, but it does not tackle the problems of other forms of contamination that occur all year around. For better implementation of ultrasound in water treatment, the use of moderate to high ultrasonic power and long treatment should be applied for such applications. There is a very limited work conducted on the use of high-power ultrasound in combination with coagulation such as the work performed by Ziylan and Ince [100]. However, this work only focused on DOC removal levels, while DOC structural change and downstream effects of the treatment were not investigated. These factors were explored in [74], and it was found that ultrasound is not only capable of removing contaminants, but it also alters the structure of remnant contaminants making them more amenable to downstream treatment processes. It was also observed that ultrasound application eliminated scum formation and resulted in more compact coagulation/flocculation sludge.
\nUltrasound technology has been harnessed by many investigations for alleviating fouling problems in membrane filtration. Ultrasound-assisted membrane technology can be applied in two ways: cleaning or pre-treatment techniques. Ultrasonic cleaning of membrane filtration can be performed directly or indirectly. In direct ultrasonic-membrane cleaning, there is no barrier that isolates the membrane from ultrasound irradiation [57]. In an indirect ultrasonic-membrane cleaning, the membrane is isolated from ultrasonic irradiation by the membrane cell body. Most of the reports regarding ultrasound-cleaning membranes dealt with flat sheet membranes; however, in a few cases, ultrasound was also used for cleaning hollow fiber membrane modules [101] and capillary membrane fibers [102].
\nAlthough ultrasonic cleaning has been recognized by many studies as an effective alternative to chemical cleaning, there are still some shortcomings that limit its application in membrane fouling control such as dependence of cleaning effectiveness on the distance between the effective cavitational region and membrane and the detrimental effect on membrane construction materials, as shown in Figure 5. Deteriorating the structure of the membrane filter could potentially lead to a failure in filtration. Thus, the direct interaction between ultrasonic irradiation and membrane should be avoided, especially for high-power applications (up to and beyond cavitation).
\nIllustration of negative effects of direct high-power ultrasound on membrane structure.
As a pre-filtration process, it was found that ultrasound is capable of reducing bio-fouling formation in membrane systems [103]. Ultrasound can also remove other contaminants, as indicated in Figure 2. In spite of the advantages of ultrasound as a filtration pre-treatment, there are some concerns related to the disintegration of the contaminants into smaller sizes, which may then lead to a pore-plugging type of fouling [104]. For this reason, distancing ultrasound from the filtration process is recommended.
\nUltrasound is recognized as the most effective disinfection technique for all forms of microbial contamination even for recalcitrant microbes and spores [47, 49, 77, 105, 106, 107]. As explained in Section 3.2, the powerful biocidal effects of ultrasound are attributed to the strong chemical and mechanical effects produced from cavitational bubble’s collapse. Disinfection is typically applied after filtration at the end of the surface water treatment process. The purpose of disinfection is to disinfect water onsite and prevent microbial growth in the water while moving within the distribution network. However, as ultrasound has no residual effect, it would be more beneficial to apply ultrasound in the earlier stages of surface water treatment.
\nThe recent challenges in drinking water treatment industry emanating from the ever-increasing contamination sources and the application of traditional chemical treatment methods have been highlighted in this chapter. Integrating physical techniques into the conventional drinking water treatment scheme has been proposed as a potential solution for these challenges. Among the common physical techniques, ultrasound technology appears to be the most promising option. Ultrasound can produce powerful effects associated with the generation and collapse of unstable bubbles. These effects are capable of destructing microbes and mineralize organic contaminants through the production of highly oxidant species and strong mechanical effects. Appropriate utilization of ultrasound effects can only be achieved through understanding the relationship between ultrasonic parameters and the properties of the water being treated. The effect of some ultrasonic parameters such as power and frequency are extensively investigated for different treatment goals; however, this chapter attempts to draw the attention to other equally important parameters such as techniques of ultrasonic wave generation, mode of operation, and the shape of the generated waves. It appears that the best ultrasonic settings for water treatment application are moderate to high power for long treatment time, low frequency, pulsed mode, and square wave generated using magnetostrictive transducer. After critical evaluation of the possible combination scenarios of ultrasound with main drinking water treatment processes, it was concluded that applying ultrasound prior to coagulation is the most beneficial option as other combinations may create adverse downstream effects. Hence, further in-depth investigation for the suggested combination is recommended for future research work.
\nThe authors declare no conflict of interest.
Supporting women in scientific research and encouraging more women to pursue careers in STEM fields has been an issue on the global agenda for many years. But there is still much to be done. And IntechOpen wants to help.
",metaTitle:"IntechOpen Women in Science Program",metaDescription:"Supporting women in scientific research and encouraging more women to pursue careers in STEM fields has been an issue on the global agenda for many years. But there is still much to be done. And IntechOpen wants to help.",metaKeywords:null,canonicalURL:null,contentRaw:'[{"type":"htmlEditorComponent","content":"At IntechOpen, we’re laying the foundations for the future by publishing the best research by women in STEM – Open Access and available to all. Our Women in Science program already includes six books in progress by award-winning women scientists on topics ranging from physics to robotics, medicine to environmental science. Our editors come from all over the globe and include L’Oreal–UNESCO For Women in Science award-winners and National Science Foundation and European Commission grant recipients.
\\n\\nWe aim to publish 100 books in our Women in Science program over the next three years. We are looking for books written, edited, or co-edited by women. Contributing chapters by men are welcome. As always, the quality of the research we publish is paramount.
\\n\\nAll project proposals go through a two-stage peer review process and are selected based on the following criteria:
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\\n\\n“My scientific path has given me the opportunity to work with colleagues all over Europe, including Germany, France, and Norway. Editing the book Graph Theory: Advanced Algorithms and Applications with IntechOpen emphasized for me the importance of providing valuable, Open Access literature to our scientific colleagues around the world. So I am highly enthusiastic about the Women in Science book collection, which will highlight the outstanding accomplishments of women scientists and encourage others to walk the challenging path to becoming a recognized scientist." Beril Sirmacek, TU Delft, The Netherlands
\\n\\nAdvantages of Publishing with IntechOpen
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\n\nWe aim to publish 100 books in our Women in Science program over the next three years. We are looking for books written, edited, or co-edited by women. Contributing chapters by men are welcome. As always, the quality of the research we publish is paramount.
\n\nAll project proposals go through a two-stage peer review process and are selected based on the following criteria:
\n\nPlus, we want this project to have an impact beyond scientific circles. We will publicize the research in the Women in Science program for a wider general audience through:
\n\nInterested? If you have an idea for an edited volume or a monograph, we’d love to hear from you! Contact Ana Pantar at book.idea@intechopen.com.
\n\n“My scientific path has given me the opportunity to work with colleagues all over Europe, including Germany, France, and Norway. Editing the book Graph Theory: Advanced Algorithms and Applications with IntechOpen emphasized for me the importance of providing valuable, Open Access literature to our scientific colleagues around the world. So I am highly enthusiastic about the Women in Science book collection, which will highlight the outstanding accomplishments of women scientists and encourage others to walk the challenging path to becoming a recognized scientist." Beril Sirmacek, TU Delft, The Netherlands
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