Green Synthesis and Antioxidant Study of Silver Nanoparticles of Root Extract of <Emphasis Type="Italic">Sageretia thea</Emphasis> and Its Role in Oxidation Protection Technology

Development of environmentally friendly synthesis of nanoparticles is one of the important areas of research in nanotechnology. In present study silver naopartticles (AgNPs) of root extract of Sageretia thea (S. thea) were synthesized at room temperature. The synthesized AgNPs were characterized by UV. Visible spectroscopy (UV), scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDX), transmission electron microscopy (TEM), dynamic light scattering (DLS) and Fourier transform infrared (FT-IR) spectroscopy. Formation of AgNPs was confirmed by visual examination the colour change from yellow to brick red due to surface Plasmon resonance band at 435 nm. SEM and TEM analysis of synthesized AgNPs revealed spherical morphology with average particle size 25 nm. Crystalline nature of the AgNPs in face centered cubic structure is evident from the selected area electron diffraction (SAED) and XRD pattern. The presence of elemental Ag was confirmed by EDX analysis at 3kv. Different functional groups which responsible for reduction and stabilization of reaction medium was confirmed by FTIR spectroscopy. The biosynthesized AgNPs showed strong DPPH and dye protection radical scavenging assay while modest hydrogen peroxide radical scavenging assay as compare to crude extract. The present investigations suggest that biosynthesized nanoparticles have a high potential for use in the preparation of drugs used against various diseases and also a promising candidate for many medical applications.     

Thiourea leaching gold and silver from the printed circuit boards of waste mobile phones

The present communication deals with the leaching of gold and silver from the printed circuit boards (PCBs) of waste mobile phones using an effective and less hazardous system, i.e., a thiourea leaching process as an alternative to the conventional and toxic cyanide leaching of gold. The influence of particle size, thiourea and Fe(3+) concentrations and temperature on the leaching of gold and silver from waste mobile phones was investigated. Gold extraction was found to be enhanced in a PCBs particle size of 100 mesh with the solutions containing 24 g/L thiourea and Fe(3+) concentration of 0.6% under the room temperature. In this case, about 90% of gold and 50% of silver were leached by the reaction of 2h. The obtained data will be useful for the development of processes for the recycling of gold and silver from the PCBs of waste mobile phones.     

Green Synthesis of Silver Nanoparticles and Study of Their Antimicrobial Properties

One of the major disadvantages of polymers when used in food-contact applications is that they are very susceptible to microbial attack. On the other hand, silver nanoparticles have received increased attention as novel antimicrobial agents. Therefore, the introduction of silver nanoparticles into conventional polymers results in new materials with improved properties. In this investigation, colloidal silver nanoparticles using an environmentally friendly procedure were synthesized. An aqueous solution of AgNO₃ was used as a silver precursor with ‘green’ reducing agents either different types of honey, or β-d-glucose. In the first case, different pH values, as well as the addition of poly(ethylene glycol), PEG were studied, while in the latter, the effect of reduction time in the presence of PEG with various average molecular weights was examined. Properties of the nanoparticles were measured using X-Ray diffraction, UV–Vis and FTIR spectroscopy. Using honey it seems that spherical particles are produced with the smaller average particle size obtained at pH 8.5. Use of honey has the advantage of being a natural product, although its main drawback is that its composition varies and it cannot be predefined to result in reproducible results. Use of β-d-glucose results in stable silver nanoparticles with small average particle size after 24 h reduction. The addition of low molecular weight PEG seems to be beneficial in the production of stable nanoparticles. Finally, the antimicrobial activity of the nanoparticles produced was investigated at different concentrations on both Gram positive and negative bacteria, such as Bacillus cereus, Bacillus subtilis, Escherichia coli and Staphylococcus aureus.     

New Poly(aniline-<Emphasis Type="Italic">co</Emphasis>-<Emphasis Type="Italic">o</Emphasis>-phenylenediamine)/Kaolinite Microcomposites for Water Decontamination

Copolymers of aniline and o-phenylenediamine/kaolinite composites were synthesized by 5:1 molar ratios of the respective monomers with different percentages of nanoclay via modified in situ chemical co-polymerization. The results were verified by measuring the FT-IR and UV–vis absorption spectra for PANI-o-PDA/kaolinite composites. The thermal behaviour of the copolymer and composites was studied. PANI-o-PDA/kaolinite composites were thermally more stable than pure copolymer. Surface morphology of copolymer composites was recorded at different magnification power by SEM which revealed whitish micrometric beads distributed all over the field with particle size in the range of 0.122–0.233 μm. This work demonstrates that the PANI-o-PDA/kaolinite composites particles can be considered as potential adsorbents for hazardous and toxic metal ions of water from lake El-Manzala, Egypt. All of Cd(II), Cu(II), and Pb(II) posed dangerous health risk to the local population via fish consumption.     

Exfoliation and Decoration of Graphene Sheets with Silver Nanoparticles and Their Antibacterial Properties

High quality graphene sheets (GRP) have been exfoliated using facile one pot method through direct ultrasonication of graphite in the presence of polyvinyl alcohol. The GRP were decorated with silver nanoparticles (AgNPs) producing graphene–silver nanoparticle composites. The effect of variation of graphite and silver salt mass ratios on the morphology and performance of produced composites was studied. The size of AgNPs decorated on GRP has been tuned with synthesis method optimization. The average size of AgNPs was found to be in the range of 8.6–15.6 nm. Cotton–polyester blend textile fabrics were treated with the new smart developed composite as antibacterial agent producing new composites. A significant inhibition of bacterial growth has been observed for graphene–silver nanoparticle composite and the antibacterial efficiency was optimized. The clear inhibition zone for textiles treated with new developed composite and AgNPs alone was recorded as 12 and 1.75 mm respectively, achieving more than six fold improvement.     

Laboratory waste minimization by recovery of silver as nano-silver colloidal dispersion from waste silver chloride

The use of cyclic experiments, where the product of one reaction becomes the starting material for the next experiment, was proposed as an effective protocol for waste minimization in an educational lab. A simple, cheap and pollution-free method was developed for recovering silver as nano-silver colloidal dispersion from waste silver chloride in the laboratories of the Faculty of Health, Safety and Environment. Silver nanoparticles of the size 5–18 nm were recovered in the presence of sodium borohydride as a reducing agent and polyvinylpyrrolidone as a stabilizer agent. The nano-silver particles were studied for their formation, structure, stability and size using UV–Vis spectroscopy, transmission electron microscopy and dynamic light scattering techniques. The antibacterial assays of nanoparticles showed satisfactory results for Escherichia coli ATCC25922, Staphylococcus aureus ATCC 29213, and Acinetobacter baumanii (Clinical isolate). A laboratory experiment was designed in which students synthesize yellow colloidal silver solution from chemical waste silver chloride and estimate particle size using visible spectroscopy.     

Correlation study of hazardous waste characteristics among various chemical processes in Republic of Korea

To harmonize with international standards, the Republic of Korea is in the process of converting its current hazardous waste classification system and setting up regulatory standards for all toxic substances present in hazardous waste. Detailed characterization of each form of hazardous waste belonging to five chemical processes and their correlations were studied. In the present work, the concentrations of 13 heavy metals, F^?, CN^?, 7 PAH compounds, total PCDD/F and 7 PCB isomers present in the hazardous waste generated among chemical processes such as synthetic rubber (SR), man-made fibers (MF), organic dyes and pigments (DP), pharmaceuticals and cosmetics were analyzed along with their leaching characteristics. Comparing all the processes, most of the heavy metal concentrations were high in SR waste. Naphthalene was the dominant PAH in most of the chemical process waste. PCDD/F concentrations of the samples were in the range of 0.001–0.003 ng I-TEQ/g. PCB isomer-101 and isomer-118 were found to be slightly higher than the permissible limit in the SR filter cake sample. SR process wastes doesn’t show any resemblance with the other process waste in either the heavy metals and PAH trend. Each sample from DP and MF were suitable only for hazardous waste landfill.     

Exploration of the Effect of Chitosan and Crosslinking Agent Concentration on the Properties of Dual Responsive Chitosan-g-Poly (N-Isopropylacrylamide) Co-polymeric Particles

The objective of the present study was to synthesize and evaluate the effect of change in concentration of chitosan (CS) and N,N-methylenebisacrylamide (MBA)- a cross linking agent, on various properties such as lower critical solution temperature (LCST), zeta potential, particle size and poly dispersity index (PDI) of the synthesized co-polymer. Nine different formulations of chitosan-g-poly (N-isopropylacrylamide) (CS-g-PNIPAAm) co-polymer with varying CS and MBA concentrations were synthesized by a surfactant free dispersion copolymerization method. The synthesized co-polymer was further characterized and confirmed for its structure, morphology, particle size, zeta-potential, thermo and pH responsive properties, in-vitro cyto-compatability and stability studies using various analytical tools. The data confirms the successful synthesis of co-polymer. The increase in the concentrations of CS and MBA during the polymerization of co-polymer, resulted in proportional increase of LCST and zeta potential with decrease in particle size of co-polymeric nanoparticles. pH responsive studies showed that as the pH of the medium increases particle size and zeta potential decreases with increase in LCST of co-polymeric nanoparticles. From the results, it can be inferred that the synthesized co-polymeric nanoparticles exerted thermo and pH responsive properties with biocompatibility. By varying the CS and MBA concentrations in the co-polymer, desired LCST, particle size and zeta potential for co-polymeric nanoparticles can be obtained and thus the synthesized co-polymer may have great potential to be used as a drug carrier (nanoform) with both thermo and pH responsiveness.     

Photo-Stabilisation and UV Blocking Efficacy of Coated Macro and Nano-Rutile Titanium Dioxide Particles in Paints and Coatings

Surface treated macro and nanoparticle TiO₂ samples have been prepared, characterised and their efficiency as UV blockers evaluated in clear coatings and paints. The particle size of the ‘base’ TiO₂ has been optimised to block UV radiation and the surface treatment developed to deactivate the photocatalytic activity of the surface of the TiO₂ particles. The resultant UV blockers have been evaluated in both solvent and water-based clear coatings. Nanoparticle TiO₂ has been prepared from ‘seed’ and the particle size was controlled by calcination. It was found that the choice of particle size is a compromise between UVA absorption, UVB absorption, visible transmission and photoactivity. It has been demonstrated that TiO₂ with a crystallite size of 25 nm yields a product with the optimum properties. A range of dispersants was successfully used to disperse and mill the TiO₂. Both organic and inorganic dispersants were used; 2-amino-2-methyl-1-propanol and 1-amino-2-propanol (MIPA) and P₂O₅ and Na₂SiO₃ respectively. The surface of the nano-TiO₂ was coated with mixed oxides of silicon, aluminium, zirconium and phosphorous. Addition of the resultant coated nano-rutiles to an Isocyanate Acrylic clear coating prolonged the lifetime of that coating compared to the blank. Generally, a surface treatment based on SiO₂, Al₂O₃ and P₂O₅ was more successful than one based on ZrO₂, Al₂O₃ and P₂O₅. Higher addition levels of the surface treatment were beneficial for protecting the polymeric coating. The UV blocker products were also evaluated in a water-based acrylic, first a water-based dispersion of the UV blocker was prepared before addition to the acrylic. The dispersions and resultant acrylic thin films were evaluated using UV/Vis spectroscopy and durability assessed. The ratio of absorbance at 300:500 nm for the water-based dispersion was shown to be a good predictor of both the transparency of the resultant acrylic thin film and the durability of that film, in terms of weight loss. Macro grade titanium dioxide pigments were also prepared and coated with treatments of silica, alumina and siloxane and their photo-stabilising activity in alkyd paint film assessed and found to be directly related to the electron–hole pair mobility and trapping as determined by micro-wave spectroscopy.     

Development of Water-Borne Green Polymer Used as a Potential Nano Drug Vehicle and its In Vitro Release Studies

This paper describes an ecofriendly development of a nanodrug delivery vehicle from seed oil. The entire synthesis, starting from the ZnO nanoparticle to the polymeric vehicle is purely microwave assisted with minimal usage of organic solvents. Multifunctional features like enhanced UV absorbance, antimicrobial properties and appreciable in vitro release can be attributed to the nanoparticle loaded polymeric vehicle. Characterization of the synthesized species was done through FT-IR, ¹HNMR, SEM and XRD. The physical characterizations were carried out using conventional laboratory techniques.     

The adsorption characteristics of heavy metals by various particle sizes of MSWI bottom ash

The incineration rate of municipal solid waste (MSW) has been increased because of difficulty in securing a proper disposal site for MSW in Korea. The advantage of incineration is reduction of the volume of waste; however, significant amounts of bottom ash and fly ash were generated in the incineration process. Their treatment has attracted growing interest because of the potential toxicity of hazardous heavy metals. Generally, heavy metals are less released from bottom ash than from fly ash. In this study the adsorption characteristics of heavy metals were investigated using various particle sizes of MSWI bottom ash. Since bottom ash has a broad particle size distribution, it was sieved to size classes of +20, -20, -48, -80, -100 mesh. Cation exchange capacity (CEC) was analyzed by the ammonium acetate method to evaluate the potential as an adsorbent. The CEC values and surface areas increase as the range of particle size becomes finer. The adsorption experiment was conducted using synthetic (Cu and Ni) and plating rinse water as a function of reaction time (10-180 min), liquid/solid ratio (2-100) and particle size (+20 to -100 mesh), respectively. The adsorption rate increased with decreasing particle size and with increasing liquid/solid ratio; however, the removal efficiency of Cu was higher than that of Ni. In the case of plating rinse water, the adsorption rate decreased sharply at high liquid/solid ratio, and it showed over 80% of adsorption rates for Cu and Ni at an initial pH of 3.     

How chemically stable is stabilized hazardous waste?

Bioassays can provide meaningful information about the relative toxicity of remediated soil samples, revealing the unwelcome toxic side effects produced by some cleanup projects. Section 121 of CERCLA's 1986 amendments calls for hazardous waste site remediations to permanently and significantly reduce the volume, toxicity, and mobility of hazardous substances, pollutants, and contaminants. Traditional engineering technology has focused on reducing volume and mobility, assuming that such reduction would lead to reductions in toxicity. Environmental scientists have argued, however, that such reductions are not always the result, but lack of consensus on how hazardous waste mixtures should be measured toxicologically has slowed development of integrated assessments. The aquatic and terrestrial bioassays discussed in this article are evaluated for various chemicals, mixtures of chemicals, and actual waste site chemical mixtures at a Superfund mobility reduction project in Kent, Washington. Results suggest that although remediation accomplished the primary objective of reducing mobility, it also introduced toxic effects. These tradeoffs must be viewed holistically when the ultimate performance of cleanup measures is judged.     

Fabrication and Characterization of Polyaniline Based Nano-Composite with Their Physico-Chemical and Environmental Applications

A series of organic–inorganic conducting nano polymer-matrix composite cation-exchanger have been synthesized via sol–gel method and characterized through FTIR, XRD, TGA-DTA, SEM, and TEM studies. The structural studies confirm the semi-crystalline nature of the material but the morphology of the exchanger gets changed after incorporation of inorganic moiety. The particle size of the nano-composite was found to be 19.2 nm. The observed band gap for the different samples was found to be in the range of 3.70–4.61 eV which shows that nano-composite material covers semiconducting range but the resistivity of samples is highly dependent on the percentage of inorganic part in the composite. Further the oxidative degradation of the polymer backbone begins after the removal of trapped water successively followed by dopant and low molecular weight oligomers. During the antimicrobial screening, the nano-composite was found to be active against different strains of bacteria and fungi. Gel electrophoresis and molecular docking studies were carried out to check the interaction and mechanism of inhibition of microbial growth, respectively by studying the effect of the nano-composite with DNA-Topoisomerase-1.     

A novel method for the preparation of silver/chitosan-O-methoxy polyethylene glycol core shell nanoparticles

Uniformly sized silver/chitosan-O-methoxy polyethylene glycol (chitosan-O-MPEG) core shell nanoparticles with different degree of substitution were synthesized. Thus, N-phthaloyl chitosan is reacted with polyethylene glycol monomethyl ether iodide in the presence of silver oxide by the following steps. At first, amino groups of chitosan are protected by fourfold excess of phthalic anhydride. Then N-phthaloyl chitosan is reacted with an appropriate amount of monomethyl ether iodide in the presence of silver oxide and lastly N-phthaloyl groups are removed to yield silver/chitosan-O-MPEG core shell nanoparticles. Structure of prepared silver/chitosan-O-MPEG core shell nanoparticles have been characterized by UV/Vis spectroscopy, transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), X-ray diffraction, and scan electron microscopy (SEM-EDX). Experimental results revealed that the prepared silver core particles had the size 18?±?2?nm. Core shell structure with chitosan-O-MPEG-coating had the size 40?±?2?nm.     

Poly(Lactic Acid)-co-Aspartic Acid Copolymers: Possible Utilization in Drug Delivery Systems

The synthesis and characterization of poly(lactic acid)-co-aspartic acid copolymers (PLA-co-Asp) were presented. Subsequently, the synthesized PLA-co-Asp copolymers were tested as biodegradable carriers in drug delivery systems. PLA-co-Asp copolymers were synthesized by solution polycondensation procedure, using different molar ratios PLA/l-aspartic acid (2.33/1, 1/1, 1/2.33), manganese acetate and phosphoric acid as catalysts and N,N′-dimethyl formamide (DMF)/toluene as solvent mixture. The copolymers were characterized by FT-IR and ¹H-NMR spectroscopy, gel permeation chromatography (GPC), DSC and TG-DTG analyses. Diclofenac sodium, a non steroidal anti-inflammatory drug was subsequently loaded into PLA-co-Asp copolymers. The in vitro drug release experiments were done by dialysis of the copolymer/drug systems, in phosphate buffer solution (pH = 7.4, at 37 °C) and monitored by UV spectroscopy.     

Environmentally Friendly Oil-Modified Polyesters as Polymeric Plasticizers for Poly(vinyl chloride)

Oil-modified polyesters were synthesized to serve as polymeric plasticizers for PVC. A total of four polymeric plasticizers with different average molecular weights were prepared. Characterizations were done using Fourier-transformed infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, and gel permeation chromatography. Some of the tests conducted on PVC films include thermal stability test using thermogravimetric analyser, determination of glass transition temperature (T_g), plasticizer migration and leaching resistance test, morphology study of plasticized PVC films using field emission scanning microscope, toxicity test, and tensile test. Owing to the plasticizing effect of the palm oil-based compound, T_g of the plasticized PVC has decreased to an average of 65 °C at 20 wt% loading. The polymeric plasticizer is also able to contribute positively to the thermal stability and mechanical properties of the PVC films. Some of the advantages of incorporating polymeric plasticizer with high molecular weight includes lower rate of leaching from plastic, and improved tensile strength and elongation at break. Besides, thermal stability of the plastic studied using Kissinger’s and Flynn–Wall–Ozawa’s approaches shows that PVC blended with high molecular weight oil-modified polyester is more thermally stable, evidenced by the increase in the activation energy of decomposition, E_d. Toxicity test using brine shrimp egg shows encouraging results, where the oil-based plasticizer is considerably less toxic compared to some of the commercial plasticizers.     

The use of the removable thin film coating technique as an alternative to traditional decontamination methods to mitigate and abate hazardous particulates

This article summarizes a study that evaluated a new decontamination technique for the mitigation and abatement of hazardous dust and particulates. Traditional decontamination methods are time‐consuming, expensive, can create airborne hazards, and do not always bring the concentration of the contaminant to acceptable levels. The use of the removable thin film coating will increase efficiency, will not generate airborne hazards, will decrease costs, and, with one application, will bring the hazardous dust concentrations to acceptable levels. Qualitative tests demonstrated that the removable thin film coating reduced the amount of visible luminescent dust (a surrogate for hazardous dust) from various surfaces. It also indicated that wherever there were minute scratches, the coating did not remove all of the dust. However, the qualitative tests showed that this decontamination method worked well as a preventative method, protecting clean areas from becoming contaminated when exposed to the luminescent dust. Further investigation was conducted using a scanning electron microscope (SEM) and carbon dust. Overall, the SEM experiment demonstrated that there was a statistically significant (p = 0.00007) removal of carbon dust (less than 10 μm in size) from surfaces with crevasses larger than 3 μm. The SEM also revealed that there were some limitations where there were large clusters of carbon dust; in these instances, the coating would tear and remain on the sample surface. One method to resolve this limitation involved adding Kevlar^TM fibers to the removable thin film coating. It was thought that this would increase the strength of the coating and eliminate the coating from tearing when removing large clusters of a contaminant. Unfortunately, this did not alleviate the issue. The use of an engineered textile, saturated with the coating, appeared to eliminate the problem with the coating not being able to remove the contaminant from the minute surface scratches and improved the removal process of the coating. © 2008 Wiley Periodicals, Inc.     

Fabrication of Biodegradable Superabsorbent Using RSM Design for Controlled Release of KNO<Subscript>3</Subscript>

Present study envisaged the sequential experimental design approach for the development of biodegradable Gelatin-Tapoica/polyacrylamide superabsorbent. Percentage water uptake efficacy of candidate sample was optimized using Response Surface Methodology (RSM) design under microwave irradiation. Different process variables such as potassium persulphate and ammonium persulphate (KPS:APS) ratio, pH, reaction time concentration of acrylamide and N,N-methylene-bis-acrylamide (MBA) were investigated as a function of percentage swelling using sequential experimental design. Maximum liquid efficacy of 1550% was obtained at KPS:APS?=?1.0:0.5; acrylamide?=?7.67?×?10^?1 mol L^?1; MBA?=?1.76?×?10^?2 mol L^?1; pH 10 and time?=?110 s. The 3D crosslinked network formed was characterized using Fourier Transformation Infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscopic (SEM) techniques and thermal stability was ensured by Thermal gravimetric Analysis/Differential Thermal Analysis/Differential Thermal Gravimetric (TGA/DTA/DTG) studies. Superabsorbent synthesized could increase the moisture content in different type of soils and was found to enhance the water-holding capability of the soil upto 60 days in clayey, 40 days in sandy and 51 days in mixture of two soils under controlled conditions. Further, candidate polymer was investigated for the in-vitro controlled release of the KNO₃ with diffusion exponent ‘n’ was found to be 0.4326 indicating Fickian type diffusion. Also, initial diffusion coefficient (D_I?=?3.49?×?10^?5 m² h^?1) was found to be greater than the lateral diffusion coefficient (D_L?=?3.76?×?10^?6 m² h^?1) indicated rapid release of KNO₃ during initial hours with slow release afterwards. The ecofriendly nature of the synthesized polymer was also tested by conducting biodegradation studies and it was found to degrade upto 94% and 88.1% within 70 days with degradation rate of 1.34 and 1.26% per day using composting method and vermicomposting method respectively. So, the synthesized candidate polymer was found to be boon for agriculture-horticulture sector with wide applicability.     

Improvement of Impact Toughness of Biodegradable Poly(butylene succinate) by Melt Blending with Sustainable Biobased Glycerol Elastomers

Poly(butylene succinate) (PBS) was melt blended with glycerol based polyesters (PGS) synthesized from pure and technical glycerol aiming to improve the impact strength of PBS. It was found that after addition of 30 wt% PGS to PBS its impact strength was significantly increased by 344% (from 31.9 to 110 J/m) and its elongation at break was maintained at 220%. Infrared spectra of the blends showed the presence of hydroxyl groups from the PGS phase suggesting that hydrogen bonding between the phases could be responsible for a good stress transfer and an efficient toughening in the PBS/PGS blends. Scanning electron microscopy imaging showed a good dispersion of PGS phase into PBS with a PGS particle size of 10 μm and less and no agglomeration. Addition of PGS to PBS was shown to be an effective strategy for improvement of PBS impact resistance without serious detrimental effects on its thermal and rheological properties.