Science.gov

Sample records for green chemical syntheses

  1. ADVANCES IN GREEN CHEMISTRY: CHEMICAL SYNTHESES USING MICROWAVE IRRADIATION, ISBN 81-901238-5-8

    EPA Science Inventory

    16. Abstract Advances in Green Chemistry: Chemical Syntheses Using Microwave Irradiation
    Microwave-accelerated chemical syntheses in solvents as well as under solvent-free conditions have witnessed an explosive growth. The technique has found widespread application predomi...

  2. Biomedical applications and chemical nature of three dyes first synthesized by Raphael Meldola: isamine blue, Meldola's blue and naphthol green B.

    PubMed

    Hope-Roberts, M; Horobin, R W

    2012-05-01

    Brief accounts are given of the chemical nature, and past and current biomedical applications of three dyes first synthesized by Raphael Meldola: isamine blue, Meldola's blue and naphthol green B. PMID:22149360

  3. White biotechnology for green chemistry: fermentative 2-oxocarboxylic acids as novel building blocks for subsequent chemical syntheses.

    PubMed

    Stottmeister, U; Aurich, A; Wilde, H; Andersch, J; Schmidt, S; Sicker, D

    2005-12-01

    Functionalized compounds, which are difficult to produce by classical chemical synthesis, are of special interest as biotechnologically available targets. They represent useful building blocks for subsequent organic syntheses, wherein they can undergo stereoselective or regioselective reactions. "White Biotechnology" (as defined by the European Chemical Industry [ http://www.europabio.org/white_biotech.htm ], as part of a sustainable "Green Chemistry,") supports new applications of chemicals produced via biotechnology. Environmental aspects of this interdisciplinary combination include: Use of renewable feedstock Optimization of biotechnological processes by means of: New "high performance" microorganisms On-line measurement of substrates and products in bioreactors Alternative product isolation, resulting in higher yields, and lower energy demand In this overview we describe biotechnologically produced pyruvic, 2-oxopentaric and 2-oxohexaric acids as promising new building blocks for synthetic chemistry. In the first part, the microbial formation of 2-oxocarboxylic acids (2-OCAs) in general, and optimization of the fermentation steps required to form pyruvic acid, 2-oxoglutaric acid, and 2-oxo-D-gluconic acid are described, highlighting the fundamental advantages in comparison to chemical syntheses. In the second part, a set of chemical formula schemes demonstrate that 2-OCAs are applicable as building blocks in the chemical synthesis of, e.g., hydrophilic triazines, spiro-connected heterocycles, benzotriazines, and pyranoic amino acids. Finally, some perspectives are discussed. PMID:15995855

  4. Shape dependent heat transport through green synthesized gold nanofluids

    NASA Astrophysics Data System (ADS)

    John, Jisha; Thomas, Lincy; Kumar, B. Rajesh; Kurian, Achamma; George, Sajan D.

    2015-08-01

    Nanofluids hold promise as a more efficient coolant for thermoelectric devices. Despite the capability of tailoring the thermo physical properties of nanofluids, by tuning the particle parameters such as shape, size and concentration, the toxicity of chemicals used for the preparation of nanoparticles is a serious concern. Green synthesis of nanoparticles is emerging as an alternative to the conventional chemical and physical methods for the preparation of nanoparticles. In this work, the results of the preparation of gold nanoparticles using plant extracts as reducing agents are presented. The green synthesis route employed for the present study provides particles of similar size, but the shape of the particles is found to vary depending upon the source of the natural reducing agents. The thermal diffusivity values of the gold nanofluid measured using laser based dual beam thermal lens technique elucidate the role of shape and concentration of the green synthesized nanoparticles on the effective thermal diffusivity values of the nanofluids.

  5. Characterization and Biocompatibility of ``Green'' Synthesized Silver Nanoparticles

    NASA Astrophysics Data System (ADS)

    Moulton, Michael; Kunzelman, Samantha; Braydich-Stolle, Laura; Nadagouda, M.; Varma, R.; Hussain, Saber

    2008-10-01

    With ever increasing emphasis on nanotechnology, silver nanoparticle are being considered for many antimicrobial needs ranging from catheter coatings, to burn wound bandages. Current synthesis methods for creating silver nanoparticles typically call for potentially hazardous chemicals, extreme heat, and produce environmentally dangerous byproducts. As a culture intent on reducing our carbon footprint on the earth, societies' focus has turned to ``green'' production capabilities. Therefore, if nanotechnology is to continue to grow at its current rate it is essential that novel ``green'' synthesis of nanoparticles becomes a reality. Furthermore, with the current and near-future applications of silver nanoparticles in biological systems it is imperative to fully analyze the potential toxic effects of these nanoparticles. In this study we have shown that by reducing silver nitrate in solutions of tea extract or epinephrine of varying concentrations spherical silver nanoparticle are formed. Furthermore, evaluation of mitochondrial function (MTS) and membrane integrity (LDH) in alveolar rat macrophages and human keratinocytes showed that these ``green'' synthesized silver nanoparticles were nontoxic.

  6. Green chemistry for chemical synthesis

    PubMed Central

    Li, Chao-Jun; Trost, Barry M.

    2008-01-01

    Green chemistry for chemical synthesis addresses our future challenges in working with chemical processes and products by inventing novel reactions that can maximize the desired products and minimize by-products, designing new synthetic schemes and apparati that can simplify operations in chemical productions, and seeking greener solvents that are inherently environmentally and ecologically benign. PMID:18768813

  7. ‘GREENER’ CHEMICAL SYNTHESES USING MICROWAVES

    EPA Science Inventory

    The diverse nature of chemical entities requires various green strategic pathways in our quest towards attaining sustainability. A solvent-free approach that involves microwave (MW) exposure of neat reactants (undiluted) catalyzed by the surfaces of less-expensive and recyclable ...

  8. A green chemistry approach for synthesizing biocompatible gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Gurunathan, Sangiliyandi; Han, JaeWoong; Park, Jung Hyun; Kim, Jin-Hoi

    2014-05-01

    Gold nanoparticles (AuNPs) are a fascinating class of nanomaterial that can be used for a wide range of biomedical applications, including bio-imaging, lateral flow assays, environmental detection and purification, data storage, drug delivery, biomarkers, catalysis, chemical sensors, and DNA detection. Biological synthesis of nanoparticles appears to be simple, cost-effective, non-toxic, and easy to use for controlling size, shape, and stability, which is unlike the chemically synthesized nanoparticles. The aim of this study was to synthesize homogeneous AuNPs using pharmaceutically important Ganoderma spp . We developed a simple, non-toxic, and green method for water-soluble AuNP synthesis by treating gold (III) chloride trihydrate (HAuCl4) with a hot aqueous extract of the Ganoderma spp . mycelia. The formation of biologically synthesized AuNPs (bio-AuNPs) was characterized by ultraviolet (UV)-visible absorption spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Furthermore, the biocompatibility of as-prepared AuNPs was evaluated using a series of assays, such as cell viability, lactate dehydrogenase leakage, and reactive oxygen species generation (ROS) in human breast cancer cells (MDA-MB-231). The color change of the solution from yellow to reddish pink and strong surface plasmon resonance were observed at 520 nm using UV-visible spectroscopy, and that indicated the formation of AuNPs. DLS analysis revealed the size distribution of AuNPs in liquid solution, and the average size of AuNPs was 20 nm. The size and morphology of AuNPs were investigated using TEM. The biocompatibility effect of as-prepared AuNPs was investigated in MDA-MB-231 breast cancer cells by using various concentrations of AuNPs (10 to 100 μM) for 24 h. Our findings suggest that AuNPs are non-cytotoxic and biocompatible. To the best of our knowledge

  9. A green chemistry approach for synthesizing biocompatible gold nanoparticles.

    PubMed

    Gurunathan, Sangiliyandi; Han, JaeWoong; Park, Jung Hyun; Kim, Jin-Hoi

    2014-01-01

    Gold nanoparticles (AuNPs) are a fascinating class of nanomaterial that can be used for a wide range of biomedical applications, including bio-imaging, lateral flow assays, environmental detection and purification, data storage, drug delivery, biomarkers, catalysis, chemical sensors, and DNA detection. Biological synthesis of nanoparticles appears to be simple, cost-effective, non-toxic, and easy to use for controlling size, shape, and stability, which is unlike the chemically synthesized nanoparticles. The aim of this study was to synthesize homogeneous AuNPs using pharmaceutically important Ganoderma spp. We developed a simple, non-toxic, and green method for water-soluble AuNP synthesis by treating gold (III) chloride trihydrate (HAuCl4) with a hot aqueous extract of the Ganoderma spp. mycelia. The formation of biologically synthesized AuNPs (bio-AuNPs) was characterized by ultraviolet (UV)-visible absorption spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Furthermore, the biocompatibility of as-prepared AuNPs was evaluated using a series of assays, such as cell viability, lactate dehydrogenase leakage, and reactive oxygen species generation (ROS) in human breast cancer cells (MDA-MB-231). The color change of the solution from yellow to reddish pink and strong surface plasmon resonance were observed at 520 nm using UV-visible spectroscopy, and that indicated the formation of AuNPs. DLS analysis revealed the size distribution of AuNPs in liquid solution, and the average size of AuNPs was 20 nm. The size and morphology of AuNPs were investigated using TEM. The biocompatibility effect of as-prepared AuNPs was investigated in MDA-MB-231 breast cancer cells by using various concentrations of AuNPs (10 to 100 μM) for 24 h. Our findings suggest that AuNPs are non-cytotoxic and biocompatible. To the best of our knowledge

  10. A green chemistry approach for synthesizing biocompatible gold nanoparticles

    PubMed Central

    2014-01-01

    Gold nanoparticles (AuNPs) are a fascinating class of nanomaterial that can be used for a wide range of biomedical applications, including bio-imaging, lateral flow assays, environmental detection and purification, data storage, drug delivery, biomarkers, catalysis, chemical sensors, and DNA detection. Biological synthesis of nanoparticles appears to be simple, cost-effective, non-toxic, and easy to use for controlling size, shape, and stability, which is unlike the chemically synthesized nanoparticles. The aim of this study was to synthesize homogeneous AuNPs using pharmaceutically important Ganoderma spp. We developed a simple, non-toxic, and green method for water-soluble AuNP synthesis by treating gold (III) chloride trihydrate (HAuCl4) with a hot aqueous extract of the Ganoderma spp. mycelia. The formation of biologically synthesized AuNPs (bio-AuNPs) was characterized by ultraviolet (UV)-visible absorption spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Furthermore, the biocompatibility of as-prepared AuNPs was evaluated using a series of assays, such as cell viability, lactate dehydrogenase leakage, and reactive oxygen species generation (ROS) in human breast cancer cells (MDA-MB-231). The color change of the solution from yellow to reddish pink and strong surface plasmon resonance were observed at 520 nm using UV-visible spectroscopy, and that indicated the formation of AuNPs. DLS analysis revealed the size distribution of AuNPs in liquid solution, and the average size of AuNPs was 20 nm. The size and morphology of AuNPs were investigated using TEM. The biocompatibility effect of as-prepared AuNPs was investigated in MDA-MB-231 breast cancer cells by using various concentrations of AuNPs (10 to 100 μM) for 24 h. Our findings suggest that AuNPs are non-cytotoxic and biocompatible. To the best of our knowledge

  11. Electrical and optical characterization of green synthesized Gd2S3

    NASA Astrophysics Data System (ADS)

    Paul, Somnath; Sarkar, A.

    2016-05-01

    Gadolinium sulphide (Gd2S3) is a magnetic semiconductor with large band gap. Gd2S3 was synthesized following chemical and green techniques. Later process provides good stability of the nano clusters (NC) due to in-situ capping of Gd2S3 NC. It has been found that the optical band gap in Gd2S3 developed by green synthesis is lowered considerably over that in chemically synthesized Gd2S3. The green agencies used in this work are Jatropha Latex and dilute Garlic extract; both are enriched in sulphur and other organic polymer molecules. Simple observation shows that Gd2S3 NC retains residual magnetization. In this work optical and electrical characterization of the developed Gd2S3 specimens are carried out. The overall results obtained are good.

  12. Antifouling activity of green-synthesized 7-hydroxy-4-methylcoumarin.

    PubMed

    Pérez, Miriam; García, Mónica; Ruiz, Diego; Autino, Juan Carlos; Romanelli, Gustavo; Blustein, Guillermo

    2016-02-01

    In the search for new environmental-friendly antifoulants for replace metallic biocides, 7-hydroxy-4-methylcoumarin was synthesized according to green chemistry procedures. This compound was characterized by current organic analysis and its antifouling properties were firstly evaluated on the bivalve Mytilus edulis platensis in the laboratory. In the second stage, a soluble matrix antifouling coating formulated with this compound was assayed in marine environment. Laboratory experiments showed that 7-hydroxy-4-methylcoumarin was effective in inhibiting both the settlement as well as the byssogenesis of mussels. In addition, after exposure time in the sea, painted panels containing this compound showed strong antifouling effect on conspicuous species of the fouling community of Mar el Plata harbor. In conclusion, green-synthesized coumarin could be a suitable antifoulant candidate for marine protective coatings. PMID:26713560

  13. Antibacterial and catalytic activities of green synthesized silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Bindhu, M. R.; Umadevi, M.

    2015-01-01

    The aqueous beetroot extract was used as reducing agent for silver nanoparticles synthesis. The synthesized nanoparticles were characterized using UV-visible spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The surface plasmon resonance peak of synthesized nanoparticles was observed at 438 nm. As the concentration of beetroot extract increases, absorption spectra shows blue shift with decreasing particle size. The prepared silver nanoparticles were well dispersed, spherical in shape with the average particle size of 15 nm. The prepared silver nanoparticles are effective in inhibiting the growth of both gram positive and gram negative bacteria. The prepared silver nanoparticles reveal faster catalytic activity. This natural method for synthesis of silver nanoparticles offers a valuable contribution in the area of green synthesis and nanotechnology avoiding the presence of hazardous and toxic solvents and waste.

  14. Spectral Studies of UV and Solar Photocatalytic Degradation of AZO Dye and Textile Dye Effluents Using Green Synthesized Silver Nanoparticles

    PubMed Central

    Mariselvam, R.; Ranjitsingh, A. J. A.; Mosae Selvakumar, P.; Alarfaj, Abdullah A.; Munusamy, Murugan A.

    2016-01-01

    The photocatalytic degradation of the chemical dye AZO and dye effluents in different time duration has been investigated using biologically synthesized silver nanoparticles. Dye industry effluents and AZO dye undergo degradation to form harmless intermediate and colourless products following irradiation by UV and solar light in the presence of green synthesized silver nanoparticles. The degree of degradation was tested under the experimental conditions such as PH, temperature, and absorbance of the dye in UV and solar light was measured. The degradation was higher in the UV light source than in the solar light source. Green synthesized silver nanoparticles in the UV light source were found to expedite the dye degradation process. PMID:27382364

  15. Chemical syntheses of inulin and levan structures.

    PubMed

    Oscarson, Stefan; Sehgelmeble, Fernando W

    2002-11-29

    A fructofuranosyl thiglycoside donor, ethyl 6-O-acetyl-3-O-benzyl-1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2-thio-beta-D-fructofuranoside (11), designed to yield stereospecifically beta-linkages and also to allow subsequent elongation in the 6- and/or 1-positions, was prepared and used in syntheses of levan and inulin structures. DMTST-promoted glycosylation between 11 (1.3 mol equiv) and methyl beta-D-fructofuranoside 6-OH and 1-OH acceptors (3 and 6) gave stereospecifically the protected methyl levanobioside 12 and inulinobioside 17 in excellent yields (80 and 86%), respectively. Protecting group manipulations on these afforded new disaccharide 6'-OH and 1'-OH acceptors (13 and 19), which were coupled again with donor 11 (1.0 mol equiv) to yield methyl levanotrioside 14 and inulinotrioside 20 in high yields, 65 and 67%, respectively. These were transformed into new acceptors and also fully deprotected to afford the methyl glycosides of levanotriose and inulinotriose, all structures that have earlier not been accessible by chemical synthesis. PMID:12444625

  16. Green synthesized conditions impacting on the reactivity of Fe NPs for the degradation of malachite green

    NASA Astrophysics Data System (ADS)

    Huang, Lanlan; Luo, Fang; Chen, Zuliang; Megharaj, Mallavarapu; Naidu, Ravendra

    2015-02-01

    This study investigates green tea extract synthesized conditions impacting on the reactivity of iron nanoparticles (Fe NPs) used for the degradation of malachite green (MG), including the volume ratio of Fe2+ and tea extract, the solution pH and temperature. Results indicated that the reactivity of Fe NPs increased with higher temperature, but fell with increasing pH and the volume ratio of Fe2+ and tea extract. Scanning electron microscope (SEM), energy-dispersive spectrometer (EDS), Fourier transform infrared spectroscope (FTIR) and X-ray diffraction (XRD) indicated that Fe NPs were spherical in shape, their diameter was 70-80 nm and they were mainly composed of iron oxide nanoparticles. UV-visible (UV-vis) indicated that reactivity of Fe NPs used in degradation of MG significantly depended on the synthesized conditions of Fe NPs. This was due to their impact on the reactivity and morphology of Fe NPs. Finally, degradation of MG showed that 90.56% of MG was removed using Fe NPs.

  17. 'GREENER' CHEMICAL SYNTHESES USING ALTERNATE REACTION CONDITIONS

    EPA Science Inventory

    Microwave (MW) irradiation in conjunction with water as reaction media has proven to be a greener chemical approach for expeditious N-alkylation reactions of amines and hydrazines wherein the reactions under mildly basic conditions afford tertiary amines and double N-alkylation t...

  18. CHEMICAL SYNTHESES IN AQUEOUS MEDIA USING MICROWAVES

    EPA Science Inventory

    The development of efficient, selective and eco-friendly synthetic methods has remained a major focus of our research group. Microwave (MW) irradiation as alternative energy source in conjunction with water as reaction media has proven to be a successful 'greener' chemical appro...

  19. Chemical evolution - Recent syntheses of bioorganic molecules.

    NASA Technical Reports Server (NTRS)

    Stephen-Sherwood, E.; Oro, J.

    1973-01-01

    Review of the important developments that have occurred in abiological biomonomer and biopolymer synthesis since about 1967, and discussion of their significance for the field of chemical evolution and the origin of life. The major portion of the review is devoted to important developments in the abiotic formation of bioorganic monomers and their condensation to biopolymers under conditions presumed to have prevailed on the primeval earth. Special attention is given to contributions shedding light on the mechanism of synthesis and selection of amino acids and on interactions of amino acids and polypeptides with nucleotides and oligonucleotides.

  20. GREEN CHEMICAL SYNTHESIS THROUGH CATALYSIS AND ALTERNATE REACTION CONDITIONS

    EPA Science Inventory

    Green chemical synthesis through catalysis and alternate reaction conditions

    Encompassing green chemistry techniques and methodologies, we have initiated several projects at the National Risk Management Research laboratory that focus on the design and development of chemic...

  1. EFFICIENT AND GREENER CHEMICAL SYNTHESES USING MICROWAVE IRRADIATION

    EPA Science Inventory

    The diverse nature of chemical entities requires various ‘green’ strategic pathways in our quest towards attaining sustainability. A solvent-free approach involving microwave (MW) exposure of neat reactants (undiluted) catalyzed by the surfaces of less-expensive and rec...

  2. Synthesis, characterization and biocompatibility of silver nanoparticles synthesized from Nigella sativa leaf extract in comparison with chemical silver nanoparticles.

    PubMed

    Amooaghaie, Rayhaneh; Saeri, Mohammad Reza; Azizi, Morteza

    2015-10-01

    Despite the development potential in the field of nanotechnology, there is a concern about possible effects of nanoparticles on the environment and human health. In this study, silver nanoparticles (AgNPs) were synthesized by 'green' and 'chemical' methods. In the wet-chemistry method, sodium borohydrate, sodium citrate and silver nitrate were used as raw materials. Leaf extract of Nigella sativa was used as reducing as well as capping agent to reduce silver nitrate in the green synthesis method. In addition, toxic responses of both synthesized AgNPs were monitored on bone-building stem cells of mice as well as seed germination and seedling growth of six different plants (Lolium, wheat, bean and common vetch, lettuce and canola). In both synthesis methods, the colorless reaction mixtures turned brown and UV-visible spectra confirmed the presence of silver nanoparticles. Scanning electron microscope (SEM) observations revealed the predominance of silver nanosized crystallites and fourier transform infra-red spectroscopy (FTIR) indicated the role of different functional groups in the synthetic process. MTT assay showed cell viability of bone-building stem cells of mice was further in the green AgNPs synthesized using black cumin extract than chemical AgNPs. IC50 (inhibitory concentrations) values for seed germination, root and shoot length for 6 plants in green AgNPs exposures were higher than the chemical AgNPs. These results suggest that cytotoxicity and phytotoxicity of the green synthesized AgNPs were significantly less than wet-chemistry synthesized ones. This study indicated an economical, simple and efficient ecofriendly technique using leaves of N. sativa for synthesis of AgNPs and confirmed that green AgNPs are safer than chemically-synthesized AgNPs. PMID:26122733

  3. Chemical phase analysis of seed mediated synthesized anisotropic silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Bharti, Amardeep; Singh, Suman; Singla, M. L.; Goyal, Navdeep

    2015-08-01

    Noble-metal nanoparticles are of great interest because of its broad applications almost in every stream (i.e. biology, chemistry and engineering) due to their unique size/shape dependant properties. In this paper, chemical phase of seed mediated synthesized anisotropic silver nanoparticle (AgNPs) has been investigated via fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). These nanaoparticles were synthesized by seed-growth method controlled by urea and dextrose results to highly stable 12-20 nm particle size revealed by zeta potential and transmission electron microscopy (TEM).

  4. Chemical phase analysis of seed mediated synthesized anisotropic silver nanoparticles

    SciTech Connect

    Bharti, Amardeep Goyal, Navdeep; Singh, Suman; Singla, M. L.

    2015-08-28

    Noble-metal nanoparticles are of great interest because of its broad applications almost in every stream (i.e. biology, chemistry and engineering) due to their unique size/shape dependant properties. In this paper, chemical phase of seed mediated synthesized anisotropic silver nanoparticle (AgNPs) has been investigated via fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). These nanaoparticles were synthesized by seed-growth method controlled by urea and dextrose results to highly stable 12-20 nm particle size revealed by zeta potential and transmission electron microscopy (TEM)

  5. Silver-based biohybrids "green" synthesized from Chelidonium majus L.

    NASA Astrophysics Data System (ADS)

    Barbinta-Patrascu, Marcela Elisabeta; Badea, Nicoleta; Ungureanu, Camelia; Constantin, Marioara; Pirvu, Cristian; Rau, Ileana

    2016-06-01

    This paper describes an original bio-design of organic/inorganic hybrid architectures containing biomimetic membranes and celandine-nanoAg for different bioapplications. A simple, time efficient, low-cost and ecofriendly bottom-up procedure was used to build for the first time, celandine/nanoAg-based hybrids. Dipalmitoyl phosphatidylcholine bio-inspired lipid bilayers were obtained by thin film hydration method. Chlorophyll a inserted into these liposomes was used as a spectral marker to detect the changes occurred in the artificial membranes. For the first time, silver nanoparticles were eco-synthesized using an aqueous extract of celandine (Chelidonium majus L.). The physical stability of the samples was evaluated in terms of zeta potential. Chlorophyll a photonic properties (based on UV-Vis absorption and emission spectra) were used to monitor the synthesis of silver nanoparticles and of bio-based hybrids. The size of samples was monitored by Dynamic Light Scattering measurements and the morphological aspects were provided by Atomic Force Microscopy analysis. The obtained silver-based biohybrids exhibited high antioxidant activity (98.48%) and strong antimicrobial properties against Escherichia coli ATCC 8738 (offering an inhibition zone of 51 mm diameter) and presented good physical stability (zeta potential reached the value of -30.7 mV) as compared to phyto-nanoAg alone.

  6. Using Green Star Metrics to Optimize the Greenness of Literature Protocols for Syntheses

    ERIC Educational Resources Information Center

    Duarte, Rita C. C.; Ribeiro, M. Gabriela T. C.; Machado, Adélio A. S. C.

    2015-01-01

    A procedure to improve the greenness of a synthesis, without performing laboratory work, using alternative protocols available in the literature is presented. The greenness evaluation involves the separate assessment of the different steps described in the available protocols--reaction, isolation, and purification--as well as the global process,…

  7. Holistic Metrics for Assessment of the Greenness of Chemical Reactions in the Context of Chemical Education

    ERIC Educational Resources Information Center

    Ribeiro, M. Gabriela T. C.; Machado, Adelio A. S. C.

    2013-01-01

    Two new semiquantitative green chemistry metrics, the green circle and the green matrix, have been developed for quick assessment of the greenness of a chemical reaction or process, even without performing the experiment from a protocol if enough detail is provided in it. The evaluation is based on the 12 principles of green chemistry. The…

  8. Green and sustainable chemical synthesis using flow microreactors.

    PubMed

    Yoshida, Jun-ichi; Kim, Heejin; Nagaki, Aiichiro

    2011-03-21

    Several features that allow flow microreactors contribute to green and sustainable chemical synthesis are presented: (1) For extremely fast reactions, kinetics often cannot be used because of the lack of homogeneity of the reaction environment when they are conducted in batch macroreactors. Better controllability, by virtue of fast mixing based on short diffusion paths in microreactors, however, leads to a higher selectivity of the products, based on kinetics considerations. Therefore, less waste is produced. (2) Reactions involving highly unstable intermediates usually require very low temperatures when they are conducted in macrobatch reactors. By virtue of short residence times, flow microreactors enable performing such reactions at ambient temperatures, avoiding cryogenic conditions and minimizing the energy required for cooling. (3) By virtue of the precise residence time control, flow microreactors allow to avoid the use of auxiliary substances such as protecting groups, enabling highly atom- and step-economical straightforward syntheses. The development of several test plants based on microreaction technology has proved that flow microreactor synthesis can be applied to the green and sustainable production of chemical substances on industrial scales. (4) Microreactor technology enables on-demand and on-site synthesis, which leads to less energy for transportation and easy recycling of substances. PMID:21394921

  9. Size-dependent antimicrobial properties of sugar-encapsulated gold nanoparticles synthesized by a green method

    NASA Astrophysics Data System (ADS)

    Badwaik, Vivek D.; Vangala, Lakshmisri M.; Pender, Dillon S.; Willis, Chad B.; Aguilar, Zoraida P.; Gonzalez, Matthew S.; Paripelly, Rammohan; Dakshinamurthy, Rajalingam

    2012-11-01

    The antimicrobial properties of dextrose-encapsulated gold nanoparticles (dGNPs) with average diameters of 25, 60, and 120 nm (± 5) and synthesized by green chemistry principles were investigated against both Gram-negative and Gram-positive bacteria. Studies were performed involving the effect of dGNPs on the growth, morphology, and ultrastructural properties of bacteria. dGNPs were found to have significant dose-dependent antibacterial activity which was also proportional to their size. Experiments revealed the dGNPs to be bacteriostatic as well as bactericidal. The dGNPs exhibited their bactericidal action by disrupting the bacterial cell membrane which leads to the leakage of cytoplasmic content. The overall outcome of this study suggests that green-synthesized dGNPs hold promise as a potent antibacterial agent against a wide range of disease-causing bacteria by preventing and controlling possible infections or diseases.

  10. Electrochemical behavior of chemically synthesized selenium thin film.

    PubMed

    Patil, A M; Kumbhar, V S; Chodankar, N R; Lokhande, A C; Lokhande, C D

    2016-05-01

    The facile and low cost simple chemical bath deposition (CBD) method is employed to synthesize red colored selenium thin films. These selenium films are characterized for structural, morphological, topographical and wettability studies. The X-ray diffraction (XRD) pattern showed the crystalline nature of selenium thin film with hexagonal crystal structure. The scanning electron microscopy (SEM) study displays selenium nanoparticles ranging from 20 to 475nm. A specific surface area of 30.5m(2)g(-1) is observed for selenium nanoparticles. The selenium nanoparticles hold mesopores in the range of 1.39nm, taking benefits of the good physicochemical stability and excellent porosity. Subsequently, the electrochemical properties of selenium thin films are deliberated by cyclic voltammetry (CV), galvanostatic charge-discharge and electrochemical impedance spectroscopy (EIS) techniques. The selenium thin film shows specific capacitance (Cs) of 21.98Fg(-1) with 91% electrochemical stability. PMID:26896773

  11. New effective chemically synthesized anti-smallpox compound NIOCH-14.

    PubMed

    Mazurkov, Oleg Yu; Kabanov, Alexey S; Shishkina, Larisa N; Sergeev, Alexander A; Skarnovich, Maksim O; Bormotov, Nikolay I; Skarnovich, Maria A; Ovchinnikova, Alena S; Titova, Ksenya A; Galahova, Darya O; Bulychev, Leonid E; Sergeev, Artemiy A; Taranov, Oleg S; Selivanov, Boris A; Tikhonov, Alexey Ya; Zavjalov, Evgenii L; Agafonov, Alexander P; Sergeev, Alexander N

    2016-05-01

    Antiviral activity of the new chemically synthesized compound NIOCH-14 (a derivative of tricyclodicarboxylic acid) in comparison with ST-246 (the condensed derivative of pyrroledione) was observed in experiments in vitro and in vivo using orthopoxviruses including highly pathogenic ones. After oral administration of NIOCH-14 to outbred ICR mice infected intranasally with 100 % lethal dose of ectromelia virus, it was shown that 50 % effective doses of NIOCH-14 and ST-246 did not significantly differ. The 'therapeutic window' varied from 1 day before infection to 6 days post-infection (p.i.) to achieve 100-60 % survival rate. The administration of NIOCH-14 and ST-246 to mice resulted in a significant reduction of ectromelia virus titres in organs examined as compared with the control and also reduced pathological changes in the lungs 6 days p.i. Oral administration of NIOCH-14 and ST-246 to ICR mice and marmots challenged with monkeypox virus as compared with the control resulted in a significant reduction of virus production in the lungs and the proportion of infected mice 7 days p.i. as well as the absence of disease in marmots. Significantly lower proportions of infected mice and virus production levels in the lungs as compared with the control were demonstrated in experiments after oral administration of NIOCH-14 and ST-246 to ICR mice and immunodeficient SCID mice challenged with variola virus 3 and 4 days p.i., respectively. The results obtained suggest good prospects for further study of the chemical compound NIOCH-14 to create a new smallpox drug on its basis. PMID:26861777

  12. Green synthesized silver nanoparticles using Nelumbonucifera root extract for efficient protein binding, antioxidant and cytotoxicity activities.

    PubMed

    Sreekanth, T V M; Ravikumar, Sambandam; Eom, In-Yong

    2014-12-01

    Silver nanoparticles (AgNPs) with a mean particle size of ∼ 16.7 nm were synthesized using an eco-friendly reducing material, aqueous Nelumbo nucifera root extract. Rapid reduction resulted in the formation of polydispersed nanoparticles. The formation of AgNPs was characterized by surface plasmon resonance, which was determined by ultraviolet-visible (UV-Vis) spectroscopy (band at 412 nm), Fourier transform infrared spectroscopy, scanning electron microscopy-energy dispersive X-ray spectroscopy, transmission electron microscopy and X-ray diffraction. The interaction of the green synthesized AgNPs with Bovine Serum Albumin (BSA) at various temperatures was investigated. Fluorescence quenching, synchronous and resonance light scattering spectroscopy along with UV-Vis absorption studies revealed the efficient binding between BSA and the AgNPs. In addition, the AgNPs exhibited moderate antioxidant and cytotoxicity activities against HeLa cell lines. PMID:25463656

  13. In vitro anticancer potential of BaCO3 nanoparticles synthesized via green route.

    PubMed

    Nagajyothi, P C; Pandurangan, Muthuraman; Sreekanth, T V M; Shim, Jaesool

    2016-03-01

    Green synthesis of nanoparticles is a growing research area because of their potential applications in nanomedicine. Barium carbonate nanoparticles (BaCO3 NPs) were synthesized using an aqueous extract of Mangifera indica seed as a reducing agent. These particles were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Transmission electron microscopy (TEM), selected area electron diffraction (SAED), Energy-dispersive-X-ray (EDX) and X-ray photoelectron spectroscopy (XPS) analysis. HR-TEM images are confirmed that green synthesized BaCO3 NPs have spherical, triangular and uneven shapes. EDX analysis confirmed the presence of Ba, C and O. The peaks at 2θ of 19.45, 23.90, 24.29, 27.72, 33.71, 34.08, 34.60, 41.98, 42.95, 44.18, 44.85, and 46.78 corresponding to (110), (111), (021), (002), (200), (112), (130), (221), (041), (202), (132) and (113) showed that BaCO3 NPs average size was ~18.3 nm. SAED pattern confirmed that BaCO3 NPs are crystalline nature. BaCO3 NPs significantly inhibited cervical carcinoma cells, as evidenced by cytotoxicity assay. Immunofluorescence and fluorescence assays showed that BaCO3 NPs increased the expression and activity of caspase-3, an autocatalytic enzyme that promotes apoptosis. According to the results, green synthesis route has great potential for easy, rapid, inexpensive, eco-friendly and efficient development of novel multifunctional nanoparticles for the treatment of cancer. PMID:26803273

  14. Differential Toxicity Characterization of Green Alternative Chemicals

    EPA Science Inventory

    Assessing the toxicity of a chemical across all possible disease domains and understanding its dose- response behavior cost millions to tens of millions of dollars per chemical, and can take years to decades to evaluate fully. This expense and the lack of regulatory requirements ...

  15. Chemically synthesized Iron-Platinum binary alloy nanoparticles

    NASA Astrophysics Data System (ADS)

    Colak, Levent

    exhibit the chemically disordered A1 (fcc) structure. We have shown that in order to obtain the L10 phase with high magnetocrystalline anisotropy, one should heat treat the as-made nanoparticles at high temperatures (800 °C) and with long periods of annealing time (>120 min). However, aggregation and sintering were inevitable with these parameters. Therefore, we have employed several different approaches for the sintering prevention of chemically synthesized FePt NPs such as formation of FePt NPs/carbon multilayered structures by sputtering of carbon onto FePt NPs previously deposited on a silicon substrate, impregnation of NPs into ordered mesoporous silica (SBA-15) and coating the NPs with a SiO2 shell. In addition to these approaches, we also propose the use of a revolutionary technique which is the construction of hollow mesoporous zirconia shells with exactly one FePt NP in each shell. Among these methods, FePt@SBA-15 mesoporous structures, FePt@SiO2 coating and FePt@hm-ZrO2 encapsulation showed very promising results. A high coercivity value of 8.6 kOe was obtained without a significant size change by annealing at 700 °C for 2h with the FePt@SBA-15 structures. However, minor aggregation on the surface of SBA-15 or within the pores was observed due to diffusion of the NPs. The sintering problem was solved completely by the silica coating technique. We have found that higher temperatures and longer annealing times (900 °C for 24 and 48h) are necessary to develop the coercivity (˜ 13 kOe) for these NPs due to the restricted geometry. By investigating the inter-particle interactions via Henkel plots and the relaxation measurements, it is concluded that interactions (either exchange of dipolar) are absent or negligibly weak and magnetization reversal is governed by coherent rotation. When samples with multi-particle occupancy per silica shell were annealed at 900 °C for 12 h, a high coercivity value of ˜ 8 kOe was obtained at room temperature. Hence, it is

  16. Silver/polysaccharide-based nanofibrous materials synthesized from green chemistry approach.

    PubMed

    Martínez-Rodríguez, M A; Garza-Navarro, M A; Moreno-Cortez, I E; Lucio-Porto, R; González-González, V A

    2016-01-20

    In this contribution a novel green chemistry approach for the synthesis of nanofibrous materials based on blends of carboxymethyl-cellulose (CMC)-silver nanoparticles (AgNPs) composite and polyvinyl-alcohol (PVA) is proposed. These nanofibrous materials were obtained from the electrospinning of blends of aqueous solutions of CMC-AgNPs composite and PVA, which were prepared at different CMC/PVA weight ratios in order to electrospin nanofibers applying a constant tension of 15kV. The synthesized materials were characterized by means of transmission electron microscopy, scanning electron microscopy; as well as Fourier-transform infrared, ultraviolet and Raman spectroscopic techniques. Experimental evidence suggests that the diameter of the nanofibers is thinner than any other reported in the literature regarding the electrospinning of CMC. This feature is related to the interactions of AgNPs with carboxyl functional groups of the CMC, which diminish those between the later and acetyl groups of PVA. PMID:26572327

  17. Green and red luminescence in co-precipitation synthesized Pr:LuAG nanophosphor

    NASA Astrophysics Data System (ADS)

    Kumar, S. Arun; Kumar, K. Ashok; Gunaseelan, M.; Asokan, K.; Senthilselvan, J.

    2016-05-01

    Pr:LuAG nanophosphor is an effective candidate in magnetic resonance imaging coupled positron emission tomography (MRI-PET) for medical imaging and scintillator applications. LuAG:Pr (0.05, 0.15 mol%) nanoscale ceramic powders were synthesized by co-precipitation method using urea as precipitant. Effect of antisite defect on structure and luminescence behavior was investigated. Pr:LuAG nanoceramic powders are found crystallized in cubic structure by high temperature calcination at 1400 °C and it shows antisite defect. HR-SEM analysis revealed spherically shaped Pr:LuAG nanoceramic particulate powders with ˜100 nm size. By the excitation at 450 nm, Pr:LuAG nanophosphor exhibit green to red luminescence in the wavelength range of 520 to 680 nm, which is originated from multiplet transition of Pr3+ ions.

  18. Green chemicals: Searching for cleaner solvents

    SciTech Connect

    Lucas, A.

    1994-10-05

    While increased pressure from EPA has solvents producers scrambling to find greener alternatives, many say the cost effectiveness and performance characteristics of traditional technologies are such that they will not disappear quickly. Though a variety of alternative {open_quotes}green{close_quotes} solvents have been developed and commercialized, better means of solvent recovery have also come along, ensuring continued use of many organic solvents. The 1990 Clean Air Act (CAA), designed to eliminate volatile organic compounds (VOCs), ozone depleters, and other hazardous air pollutants (HAPs), has put limits on many organic solvents. Those most under fire are chlorinated solvents, such as methylene chloride, 1,1,1 trichloroethylene (methyl chloroform), and chlorofluorocarbon (CFC)-113. Producers have been developing a variety of lower VOC solvents to replace those being phased out or regulated. Among those likely to experience most growth are aliphatic hydrocarbons to replace chlorinated solvents in cleaning applications. Growth is also expected for alcohols, esters, and glycol ethers for other end-use applications.

  19. OPTIMIZING POTENTIAL GREEN REPLACEMENT CHEMICALS – BALANCING FUNCTION AND RISK

    EPA Science Inventory

    An important focus of green chemistry is the design of new chemicals that are inherently less toxic than the ones they might replace, but still retain required functional properties. A variety of methods exist to measure or model both functional and toxicity surrogates that could...

  20. A low cost, green method to synthesize GaN nanowires

    PubMed Central

    Zhao, Jun-Wei; Zhang, Yue-Fei; Li, Yong-He; Su, Chao-hua; Song, Xue-Mei; Yan, Hui; Wang, Ru-Zhi

    2015-01-01

    The synthesis of gallium nitride nanowires (GaN NWs) by plasma enhanced chemical vapor deposition (PECVD) are successfully demonstrated in this work. The simple and green synthesis route is to introduce gallium oxide (Ga2O3) and nitrogen (N2) for the growth of nanowires. The prepared GaN nanowires have a single crystalline wurtzite structure, which the length of some nanowires is up to 20 μm, with a maximum diameter about 140 nm. The morphology and quantity of the nanowires can be modulated by the growth substrate and process parameters. In addition, the photoluminescence and field emission properties of the prepared GaN nanowires have been investigated, which were found to be largely affected by their structures. This work renders an environmentally benign strategy and a facile approach for controllable structures on nanodevice. PMID:26643613

  1. Comparison of chemically and electrochemically synthesized polyaniline films

    SciTech Connect

    Hatchett, D.W.; Josowicz, M.; Janata, J.

    1999-12-01

    The electrochemical growth of thick ({approximately}2 mm) emeraldine, polyaniline (PANI{sup E}) films from solutions containing 2 M HBF{sub 4} and 0.25 M aniline is demonstrated. Electrochemically and chemically prepared PANI{sup E} films, cast from formic acid solutions, are compared. The combination of electrochemical results with Fourier transform infrared spectroscopic data indicates that pure and homogeneous standard material can be reproducibly prepared electrochemically.

  2. beta. -Sulfopyruvate: chemical and enzymatic syntheses and enzymatic assay

    SciTech Connect

    Weinstein, C.L.; Griffith, O.W.

    1986-01-01

    BETA-Sulfopyruvic acid (2-carboxy-2-oxoethanesulfonic acid) is prepared in greater than 90% yield by reaction of bromopyruvic acid with sodium sulfite. ..beta..-(/sup 35/S)Sulfopyruvate is prepared by transamination between (/sup 35/)cysteinesulfonate (cysteate) and ..cap alpha..-ketoglutarate using mitochondrial aspartate aminotransferase isolated from rat liver. Following either chemical or enzymatic synthesis the crude reaction product is conveniently purified by chromatography on Dowex 1; ..beta..-sulfopyruvate is isolated as the stable, water-soluble dilithium salt. ..beta..-Sulfopyruvate is shown to be an alternative substrate of mitochondrial malate dehydrogenase; in the presence of 0.25 mM NADH, ..beta..-sulfopyruvate is reduced with an apparent K/sub m/ of 6.3 mM and a V/sub max/ equal to about 40% of that observed with oxaloacetate. This finding forms the basis of a convenient spectrophotometric assay of ..beta..-sulfopyruvate.

  3. Novel green nano composites films fabricated by indigenously synthesized graphene oxide and chitosan.

    PubMed

    Khan, Younus H; Islam, Atif; Sarwar, Afsheen; Gull, Nafisa; Khan, Shahzad M; Munawar, Muhammad A; Zia, Saba; Sabir, Aneela; Shafiq, Muhammad; Jamil, Tahir

    2016-08-01

    Graphene oxide (GO) was indigenously synthesized from graphite using standard Hummers method. Chitosan-graphene oxide green composite films were fabricated by mixing aqueous solution of chitosan and GO using dilute acetic acid as a solvent for chitosan. Chitosan of different viscosity and calculated molecular weight was used keeping amount of GO constant in each composite film. The structural properties, thermal stability and mechanical properties of the composite films were investigated using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and tensile test. FTIR studies revealed the successful synthesis of GO from graphite powder and it was confirmed that homogenous blending of chitosan and GO was promising due to oxygenated functional groups on the surface of GO. XRD indicated effective conversion of graphite to GO as its strong peak observed at 11.06° as compared to pristine graphite which appeared at 26°. Moreover, mechanical analysis confirmed the effect of molecular weight on the mechanical properties of chitosan-GO composites showing that higher molecular weight chitosan composite (GOCC-1000) showed best strength (higher than 3GPa) compared to other composite films. Thermal stability of GOCC-1000 was enhanced for which residual content increased up to 56% as compared to the thermal stability of GOCC-200 whose residue was restricted to only 24%. The morphological analysis of the composites sheets by SEM was smooth having dense structure and showed excellent interaction, miscibility, compatibility and dispersion of GO with chitosan. The prepared composite films find their applications as biomaterials in different biomedical fields. PMID:27112859

  4. Catalytic and biological activities of green silver nanoparticles synthesized from Plumeria alba (frangipani) flower extract.

    PubMed

    Mata, Rani; Reddy Nakkala, Jayachandra; Rani Sadras, Sudha

    2015-06-01

    Herein, we report the green synthesis of silver nanoparticles using Plumeria alba (frangipani) flower extract (FFE) and their biological applications. The formation of frangipani silver nanoparticles (FSNPs) was confirmed by UV-visible spectroscopy and characterized by DLS particle size analyzer, SEM/EDAX, FTIR, TGA/DSC and XRD. The synthesized spherical FSNPs were found to be 36.19nm in size as determined by DLS particle size analyzer. EDAX data and XRD pattern of FSNPs confirmed the presence and face-centered cubic (fcc) phase structure of silver. The bioactive groups C-C and C-N present in FFE were involved in the formation of FSNPs as identified by FTIR analysis. FSNPs exhibited powerful catalytic activity by reducing 4-nitrophenol to 4-aminophenol within 8min and the other organic dyes namely methylene blue and ethidium bromide were moderately degraded. Biological activities of FSNPs are evaluated by means of antioxidant, antibacterial and cytotoxic effect. Antioxidant potential of FSNPs was assessed by various in vitro assays in which they exhibited moderate antioxidant activity. The antibacterial effect of FSNPs was tested in two different pathogenic bacterial strains and their bacteriostatic effect was confirmed by growth kinetic study in Escherichia coli. The cytotoxic effect of FSNPs in COLO 205 was analyzed by MTT assay and the IC50 concentration was found at 5.5 and 4μg/ml respectively after 24 and 48h of incubation. Cytotoxic effect of FSNPs in COLO 205 cells was associated with the loss of membrane integrity and chromatin condensation which might have played a crucial role in the induction of apoptosis as evidenced in AO/EB staining. PMID:25842128

  5. Antibacterial activity of silver bionanocomposites synthesized by chemical reduction route

    PubMed Central

    2012-01-01

    Background The aim of this study is to investigate the functions of polymers and size of nanoparticles on the antibacterial activity of silver bionanocomposites (Ag BNCs). In this research, silver nanoparticles (Ag NPs) were incorporated into biodegradable polymers that are chitosan, gelatin and both polymers via chemical reduction method in solvent in order to produce Ag BNCs. Silver nitrate and sodium borohydride were employed as a metal precursor and reducing agent respectively. On the other hand, chitosan and gelatin were added as a polymeric matrix and stabilizer. The antibacterial activity of different sizes of silver nanoparticles was investigated against Gram-positive and Gram-negative bacteria by the disk diffusion method using Mueller-Hinton Agar. Results The properties of Ag BNCs were studied as a function of the polymer weight ratio in relation to the use of chitosan and gelatin. The morphology of the Ag BNCs films and the distribution of the Ag NPs were also characterized. The diameters of the Ag NPs were measured and their size is less than 20 nm. The antibacterial trait of silver/chitosan/gelatin bionanocomposites was investigated. The silver ions released from the Ag BNCs and their antibacterial activities were scrutinized. The antibacterial activities of the Ag BNC films were examined against Gram-negative bacteria (E. coli and P. aeruginosa) and Gram-positive (S. aureus and M. luteus) by diffusion method using Muller-Hinton agar. Conclusions The antibacterial activity of Ag NPs with size less than 20 nm was demonstrated and showed positive results against Gram-negative and Gram-positive bacteria. The Ag NPs stabilized well in the polymers matrix. PMID:22967920

  6. In-vitro anticancer activity of green synthesized silver nanoparticles on MCF-7 human breast cancer cells.

    PubMed

    Jang, Suk Ju; Yang, In Jun; Tettey, Clement O; Kim, Ki Mo; Shin, Heung Mook

    2016-11-01

    In recent years, green synthesis of metallic nanoparticles is a growing area of research because of their potential applications in nanomedicine. In the present study we synthesized silver nanoparticles (silver NPs) from AgNO3 using aqueous extract of Lonicera hypoglauca flower as reducing and capping agents. The synthesized silver NPs were characterized using UV-Vis spectroscopy, FTIR, SEM-ED, TEM and SAED. Silver NPs were found to be significantly toxic to MCF-7 cells via the induction of apoptosis whereas sparing normal immune system (RAW 264.7) cells. PMID:27524038

  7. Synthesis, characterization and biocompatibility of ``green'' synthesized silver nanoparticles using tea polyphenols

    NASA Astrophysics Data System (ADS)

    Moulton, Michael C.; Braydich-Stolle, Laura K.; NadagoudaPresent Address: Pegasus Technical Services, 46 E. Hollister Street, Cincinnati, 45219, Ohio, Usa., Mallikarjuna N.; Kunzelman, Samantha; Hussain, Saber M.; Varma, Rajender S.

    2010-05-01

    Since ancient times, people have taken advantage of the antimicrobial effects of colloidal silver particles. Aside from the medical prospects, silver nanoparticles are found in a wide range of commercially available consumer products ranging from cosmetics to household cleansers. Current synthetic methods for creating silver nanoparticles typically call for potentially hazardous chemicals, extreme heat, and produce environmentally dangerous byproducts. Therefore, it is essential that novel ``green'' synthesis of nanoparticles becomes a reality, and it is imperative to fully analyze the potential toxic effects of these nanoparticles. In this study, we have shown that by reducing silver nitrate in solutions of tea extract or epicatechin of varying concentrations, spherical silver nanoparticles were formed that had controllable size distributions depending on the concentration of tea extract or epicatechin in the samples. Our ultra-resolution microscopy demonstrated that the nanoparticles were in fact interacting with the keratinocytes. Furthermore, evaluation of mitochondrial function (MTS) to assess cell viability and membrane integrity (LDH) in human keratinocytes showed that the silver nanoparticles were nontoxic. These results demonstrated that these nanoparicles are potentially biocompatible and warrant further evaluation in other biological systems.

  8. Synthesis, characterization and biocompatibility of "green" synthesized silver nanoparticles using tea polyphenols.

    PubMed

    Moulton, Michael C; Braydich-Stolle, Laura K; Nadagouda, Mallikarjuna N; Kunzelman, Samantha; Hussain, Saber M; Varma, Rajender S

    2010-05-01

    Since ancient times, people have taken advantage of the antimicrobial effects of colloidal silver particles. Aside from the medical prospects, silver nanoparticles are found in a wide range of commercially available consumer products ranging from cosmetics to household cleansers. Current synthetic methods for creating silver nanoparticles typically call for potentially hazardous chemicals, extreme heat, and produce environmentally dangerous byproducts. Therefore, it is essential that novel "green" synthesis of nanoparticles becomes a reality, and it is imperative to fully analyze the potential toxic effects of these nanoparticles. In this study, we have shown that by reducing silver nitrate in solutions of tea extract or epicatechin of varying concentrations, spherical silver nanoparticles were formed that had controllable size distributions depending on the concentration of tea extract or epicatechin in the samples. Our ultra-resolution microscopy demonstrated that the nanoparticles were in fact interacting with the keratinocytes. Furthermore, evaluation of mitochondrial function (MTS) to assess cell viability and membrane integrity (LDH) in human keratinocytes showed that the silver nanoparticles were nontoxic. These results demonstrated that these nanoparicles are potentially biocompatible and warrant further evaluation in other biological systems. PMID:20648322

  9. A chemical mixer with dark-green nails.

    PubMed

    Leung, Lawrence K; Harding, John

    2015-01-01

    Nails are integral extensions of the skin and they together form the largest organ of the human body. Changes in nail appearance can be due to external insults or internal pathologies, and nail signs have to be interpreted in light of a good history. We present an interesting case of a man who developed dark-green discolouration of his nails over a short period of time. His work as a chemical mixer rendered him susceptible to hazardous chemical exposure. A notification was filed and the local Occupational Health Department discovered insufficient protective gear and lack of protocols regarding hazards of isocyanate-based resin. The patient also reported washing utensils with bare hands. Based on the meniscal demarcation borders between the discoloured and normal areas, plus a positive bacterial culture from nail clippings, the final diagnosis of isocyanate-resin-induced onycholysis with secondary Pseudomonas infection remained as the most likely clinical diagnosis. PMID:26040827

  10. Pulsed-Thermal-Processing of Chemically Synthesized FePt Nanoparticles

    SciTech Connect

    Shi, Shifan; Kang, Shishou; Lawson, Jeremy; Jia, Zhiyong; Nikles, David E.; Harrell, J. W.; Ott, Ronald D; Kadolkar, Puja

    2006-01-01

    The disordered face-centered-cubic A1 to the chemical ordered face-centered-tetragonal L1{sub 0} phase transformation of chemically synthesized magnetic FePt nanoparticles has been studied in the millisecond regime using a pulsed high-density plasma arc light source. Under select annealing conditions, relatively high magnetic coercivities (Hc) and anisotropies (Hk) of FePt nanoparticles were obtained with the millisecond pulse processing without significant sintering of the nanoparticles.

  11. Evaluation of tetraethoxysilane (TEOS) sol-gel coatings, modified with green synthesized zinc oxide nanoparticles for combating microfouling.

    PubMed

    Krupa, A Nithya Deva; Vimala, R

    2016-04-01

    Green synthesis of zinc oxide nanoparticles (ZnO-NPs) is gaining importance as an eco-friendly alternative to conventional methods due to its enormous applications. The present work reports the synthesis of ZnO-NPs using the endosperm of Cocos nucifera (coconut water) and the bio-molecules responsible for nanoparticle formation have been identified. The synthesized nanoparticles were characterized using UV-Visible spectroscopy (UV-Vis), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Transmission Electron Microscopy (TEM) and Zeta potential measurement. The results obtained reveal that the synthesized nanoparticles are moderately stable with the size ranging from 20 to 80 nm. The bactericidal effect of the nanoparticles was proved by well diffusion assay and determination of minimum inhibitory concentration (MIC) against marine biofilm forming bacteria. Further the green synthesized ZnO-NPs were doped with TEOS sol-gels (TESGs) in order to assess their antimicrofouling capability. Different volumes of liquid sol-gels were coated on to 96-well microtitre plate and cured under various conditions. The optimum curing conditions were found to be temperature 60 °C, time 72 h and volume 200 μl. Antiadhesion test of the undoped (SG) and ZnO-NP doped TEOS sol-gel (ZNSG) coatings were evaluated using marine biofilm forming bacteria. ZNSG coatings exhibited highest biofilm inhibition (89.2%) represented by lowest OD value against Pseudomonasotitidis strain NV1. PMID:26838903

  12. Preparation and Characterization of Chemically Synthesized Hybrid Composites for Bone Tissue Regeneration

    NASA Astrophysics Data System (ADS)

    Raucci, M. G.; Guarino, V.; Ambrosio, L.

    2008-08-01

    The aim of this study concerns the development of bioresorbable composite materials for bone repair and regeneration. Hydroxyapatite loaded composites were synthesized by a colloidal non-aqueous chemical precipitation technique at room temperature. This study describes the synthesis and characterization of HA/PCL composite material, in order to verify the interaction between the ceramic and the polymer phases by a morphological investigation.

  13. Chemically synthesized lithium peroxide composite cathodes for closed system Li-O2 batteries.

    PubMed

    Bhargav, Amruth; Guo, Wei; Fu, Yongzhu

    2016-04-28

    A binder-free lithium peroxide-carbon nanofiber composite cathode was synthesized chemically to be used in a closed system lithium-oxygen battery without external supply of oxygen. This cathode enhances the closed system performance and exhibits good rechargeability with cyclability up to 50 cycles. This composite cathode provides scope for full cell development. PMID:27032704

  14. Characterization, antioxidant and cytotoxicity evaluation of green synthesized silver nanoparticles using Cleistanthus collinus extract as surface modifier

    SciTech Connect

    Kanipandian, Nagarajan; Ramesh, Ramar; Subramanian, Periyasamy

    2014-01-01

    Graphical abstract: The figure is the TEM image of green synthesized silver nanoparticles from Cleistanthus collinus. In this investigation we have used the poisonous plant as a reducing and capping agent. This is a first time data to synthesis the metal nanoparticles using poisonous plant. - Highlights: • A hitherto unreported venomous plant mediated AgNPs synthesis. • The particle size is observed in the range of 20–40 nm. • Surface morphology of the well-dispersed silver nanoparticles is studied using SEM and TEM. • Crystalline nature of AgNPs is confirmed by X-ray diffraction analysis. • Antioxidant activities of green synthesized AgNPs are tested in vitro. - Abstract: We report, here a simple green method for the preparation of silver nanoparticles (AgNPs) using the plant extract of Cleistanthus collinus as potential phyto reducer. The synthesized AgNPs were characterized by UV–vis spectra, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The obtained results confirmed that the AgNPs were crystalline in nature and the morphological studies reveal the spherical shape of AgNPs with size ranging from 20 to 40 nm. The in vitro antioxidant activity of AgNPs showed a significant effect on scavenging of free radicals. The cytotoxicity study exhibited a dose-dependent effect against human lung cancer cells (A549) and normal cells (HBL-100), the inhibitory concentration (IC{sub 50}) were found to be 30 μg/mL and 60 μg/mL respectively. The in vivo histopathology of mouse organs proved that AgNPs does not possess toxic effect and can be extensively applied in biomedical sciences.

  15. Chemical and biochemical activities of sonochemically synthesized poly(N-isopropyl acrylamide)/silica nanocomposite

    NASA Astrophysics Data System (ADS)

    Chowdhury, Pranesh; Saha, Swadhin Kr; Guha, Arun; Saha, Samar Kr

    2012-11-01

    Poly(N-isopropyl acrylamide) (PNIPA) grafted mesoporous silica nanoparticles (MPSNP) leading to novel inorganic/organic core-shell nanocomposite has been synthesized sonochemically in an aqueous medium without additives like cross-linker, hydrophobic agent, organic solvent. The colloidal stability of MPSNP is enhanced significantly due to encapsulation of the polymer. The composites are characterized by TEM, FTIR and TGA. The chemical and biochemical activities of the sonochemically synthesized materials have been studied in the light of reaction with acid-base, protein adsorption, antimicrobial activity, biocompatibility and nonthrombogenic property. Advantages of sonochemical synthesis compared to other techniques have been evaluated.

  16. Removal of malachite green dye from aqueous solution using mesoporous silica synthesized from 1-octyl-3-methylimidazolium chloride ionic liquid

    NASA Astrophysics Data System (ADS)

    Ekka, Basanti; Nayak, Soumitra Ranjan; Dash, Priyabrat; Patel, Raj Kishore

    2016-04-01

    In this research, mesoporous silica was synthesized via a modified sol-gel route using 1-octyl-3-methylimidazolium chloride and was employed to remove malachite green (MG) dye from aqueous solution. Subsequently, this material was characterized and identified by different techniques such as Fourier transform infrared spectroscopy (FT-IR), N2 adsorption-desorption method, scanning electron microscopy (SEM), and thermosgravimetric analysis (TGA). Unique properties such as high surface area and pore diameter, in addition to highly reactive atoms and presence of various functional groups make the mesoporous silica possible for efficient removal of malachite green (MG). In batch experimental set-up, optimum conditions for quantitative removal of MG by mesoporous silica was attained by varying different variables such as adsorbent dosage, initial dye concentration, contact time, and pH. Optimum values were set as pH of 8.0, 0.5 g of adsorbent at contact time of 120 min. The adsorption of MG follows the pseudo-second-order rate equation. Equilibrium data fitted well with the Freundlich model at all amount of adsorbent, while maximum adsorption capacity was 5.981 mg g-1 for 0.5 g mesoporous silica synthesized in IL.

  17. Chemoselective Reactions of Citral: Green Syntheses of Natural Perfumes for the Undergraduate Organic Laboratory

    ERIC Educational Resources Information Center

    Cunningham, Anna D.; Ham, Eun Y.; Vosburg, David A.

    2011-01-01

    Chemoselectivity is a central concept in organic synthesis and may be readily appreciated in the context of the fragrant, polyfunctional natural product citral. We describe three single-step reactions students may perform on citral to synthesize other natural perfumes: citronellal, geraniol, nerol, or epoxycitral. Each of the reactions uses a…

  18. Green, Enzymatic Syntheses of Divanillin and Diapocynin for the Organic, Biochemistry, or Advanced General Chemistry Laboratory

    ERIC Educational Resources Information Center

    Nishimura, Rachel T.; Giammanco, Chiara H.; Vosburg, David A.

    2010-01-01

    Environmentally benign chemistry is an increasingly important topic both in the classroom and the laboratory. In this experiment, students synthesize divanillin from vanillin or diapocynin from apocynin, using horseradish peroxidase and hydrogen peroxide in water. The dimerized products form rapidly at ambient temperature and are isolated by…

  19. Antimicrobial efficacy of green synthesized drug blended silver nanoparticles against dental caries and periodontal disease causing microorganisms.

    PubMed

    Emmanuel, R; Palanisamy, Selvakumar; Chen, Shen-Ming; Chelladurai, K; Padmavathy, S; Saravanan, M; Prakash, P; Ajmal Ali, M; Al-Hemaid, Fahad M A

    2015-11-01

    Development of biologically inspired green synthesis of silver nanoparticles is evolving into an important branch of nano-biotechnology. In the present investigation, we report the green synthesis of silver nanoparticles (AgNPs) employing the leaf extract of Justicia glauca. Water-soluble organics present in the leaf extract are mainly responsible for the reduction of silver nitrate (AgNO3) solution to AgNPs. The AgNPs are 10-20nm in dimensions as determined by TEM images. The antimicrobial activities of green synthesized AgNPs and drug blended AgNPs have been evaluated against the dental caries and periodontal disease causing microorganisms such as Streptococcus mutans, Staphylococcus aureus, Lactobacillus acidophilus, Micrococcus luteus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and Candida albicans. The AgNPs and drug blended AgNPs show a significant antibacterial and antifungal activity. Minimum inhibitory concentration (MIC) value of AgNPs determined against the selected dental caries and periodontal disease causing microorganisms are noticeable between the range of 25-75μg/mL. PMID:26249603

  20. Green synthesized gold nanoparticles decorated graphene oxide for sensitive determination of chloramphenicol in milk, powdered milk, honey and eye drops.

    PubMed

    Karthik, R; Govindasamy, Mani; Chen, Shen-Ming; Mani, Veerappan; Lou, Bih-Show; Devasenathipathy, Rajkumar; Hou, Yu-Shen; Elangovan, A

    2016-08-01

    A simple and rapid green synthesis using Bischofia javanica Blume leaves as reducing agent was developed for the preparation of gold nanoparticles (AuNPs). AuNPs decorated graphene oxide (AuNPs/GO) was prepared and employed for the sensitive amperometric determination of chloramphenicol. The green biosynthesis requires less than 40s to reduce gold salts to AuNPs. The formations of AuNPs and AuNPs/GO were evaluated by scanning electron and atomic force microscopies, UV-Visible and energy dispersive X-ray spectroscopies, X-ray diffraction studies, and electrochemical methods. AuNPs/GO composite film modified electrode was fabricated and shown excellent electrocatalytic ability towards chloramphenicol. Under optimal conditions, the amperometric sensing platform has delivered wide linear range of 1.5-2.95μM, low detection limit of 0.25μM and high sensitivity of 3.81μAμM(-1)cm(-2). The developed sensor exhibited good repeatability and reproducibility, anti-interference ability and long-term storage stability. Practical feasibility of the sensor has been demonstrated in food samples (milk, powdered milk and honey) and pharmaceutical sample (eye drops). The green synthesized AuNPs/GO composite has great potential for analysis of food samples in food safety measures. PMID:27153217

  1. PbO networks composed of single crystalline nanosheets synthesized by a facile chemical precipitation method

    SciTech Connect

    Samberg, Joshua P.; Kajbafvala, Amir; Koolivand, Amir

    2014-03-01

    Graphical abstract: - Highlights: • Synthesis of PbO networks through a simple chemical precipitation route. • The synthesis method is rapid and low-cost. • Each network is composed of single crystalline PbO nanosheets. • A possible growth mechanism is proposed for synthesized PbO networks. - Abstract: For the field of energy storage, nanostructured lead oxide (PbO) shows immense potential for increased specific energy and deep discharge for lead acid battery technologies. In this work, PbO networks composed of single crystalline nanosheets were synthesized utilizing a simple, low cost and rapid chemical precipitation method. The PbO networks were prepared in a single reaction vessel from starting reagents of lead acetate dehydrate, ammonium hydroxide and deionized water. Lead acetate dehydrate was chosen as a reagent, as opposed to lead nitrate, to eliminate the possibility of nitrate contamination of the final product. X-ray diffraction (XRD) analysis, high resolution scanning electron microscopy (HRSEM) and high resolution transmission electron microscopy (HRTEM) analysis were used to characterize the synthesized PbO networks. The reproducible method described herein synthesized pure β-PbO (massicot) powders, with no byproducts. A possible formation mechanism for these PbO networks is proposed. The growth is found to proceed predominately in the 〈1 1 1〉 and 〈2 0 0〉 directions while being limited in the 〈0 1 1〉 direction.

  2. CHARACTERIZATION OF CHEMICALLY MODIFIED HYPERTHERMOPHILIC ENZYMES FOR CHEMICAL SYNTHESES AND BIOREMEDIATION REACTIONS

    EPA Science Inventory

    Research developments in the area of biocatalysis in organic solvents are expected to greatly expand the role of bioprocessing in chemical synthesis, fuel processing, and bioremediation technologies. Many biological transformation reactions of interest to DOE site remediation inv...

  3. STM study of monolayer MoS2 synthesized by Chemical Vapor Deposition

    NASA Astrophysics Data System (ADS)

    Mills, Adam; Chen, Chuanhui; Yu, Yifei; Cao, Linyui; Tao, Changgang

    2014-03-01

    Monolayer molybdenum disulfide (MoS2) , an atomically thin transition-metal dichalcogenide semiconductor with a direct band gap, as opposed to an indirect band gap in bulk MoS2, has recently captured a lot of research interest for its distinctive optical and electronic properties, and potential applications such as field effect transistors, optoelectronic devices and chemical sensors. Using scanning tunneling microscopy, we have investigated monolayer MoS2 synthesized by chemical vapor deposition. The structural and electronic properties of monolayer MoS2 grown on glassy carbon and other substrates will be presented. We will also discuss our preliminary scanning tunneling spectroscopy measurements on these samples.

  4. Pretreatment of chemically-synthesized Aβ42 affects its biological activity in yeast.

    PubMed

    Porzoor, Afsaneh; Caine, Joanne M; Macreadie, Ian G

    2014-01-01

    The tendency of amyloid β (Aβ42) peptide to misfold and aggregate into insoluble amyloid fibrils in Alzheimer's disease (AD) has been well documented. Accumulation of Aβ42 fibrils has been correlated with abnormal apoptosis and unscheduled cell division which can also trigger the death of neuronal cells, while oligomers can also exhibit similar activities. While investigations using chemically-synthesized Aβ42 peptide have become common practice, there appear to be differences in outcomes from different preparations. In order to resolve this inconsistency, we report 2 separate methods of preparing chemically-synthesized Aβ42 and we examined their effects in yeast. Hexafluoroisopropanol pretreatment caused toxicity while, ammonium hydroxide treated Aβ42 induced cell proliferation in both C. glabrata and S. cerevisiae. The hexafluoroisopropanol prepared Aβ42 had greater tendency to form amyloid on yeast cells as determined by thioflavin T staining followed by flow cytometry and microscopy. Both quiescent and non-quiescent cells were analyzed by these methods of peptide preparation. Non-quiescent cells were susceptible to the toxicity of Aβ42 compared with quiescent cells (p < 0.005). These data explain the discrepancy in the previous publications about the effects of chemically-synthesized Aβ42 on yeast cells. The effect of Aβ42 on yeast cells was independent of the size of the peptide aggregates. However, the Aβ42 pretreatment determined whether the molecular conformation of peptide resulted in proliferation or toxicity in yeast based assays. PMID:25495906

  5. Spectroscopic investigations, antimicrobial, and cytotoxic activity of green synthesized gold nanoparticles.

    PubMed

    Lokina, S; Suresh, R; Giribabu, K; Stephen, A; Lakshmi Sundaram, R; Narayanan, V

    2014-08-14

    The gold nanoparticles (AuNPs) were synthesized by using naturally available Punica Granatum fruit extract as reducing and stabilizing agent. The biosynthesized AuNPs was characterized by using UV-Vis, fluorescence, high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) and thermogravimetric (TGA) analysis. The surface plasmon resonance (SPR) band at 585nm confirmed the reduction of auric chloride to AuNPs. The crystalline nature of the biosynthesized AuNPs was confirmed from the HRTEM images, XRD and selected area electron diffraction (SAED) pattern. The HRTEM images showed the mixture of triangular and spherical-like AuNPs having size between 5 and 20nm. The weight loss of the AuNPs was measured by TGA as a function of temperature under a controlled atmosphere. The biomolecules are responsible for the reduction of AuCl4(-) ions and the formation of stable AuNPs which was confirmed by FTIR measurement. The synthesized AuNPs showed an excellent antibacterial activity against Candida albicans (ATCC 90028), Aspergillus flavus (ATCC 10124), Staphylococcus aureus (ATCC 25175), Salmonella typhi (ATCC 14028) and Vibrio cholerae (ATCC 14033). The minimum inhibitory concentration (MIC) of AuNPs was recorded against various microorganisms. Further, the synthesized AuNPs shows an excellent cytotoxic result against HeLa cancer cell lines at different concentrations. PMID:24755638

  6. Spectroscopic investigations, antimicrobial, and cytotoxic activity of green synthesized gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Lokina, S.; Suresh, R.; Giribabu, K.; Stephen, A.; Lakshmi Sundaram, R.; Narayanan, V.

    2014-08-01

    The gold nanoparticles (AuNPs) were synthesized by using naturally available Punica Granatum fruit extract as reducing and stabilizing agent. The biosynthesized AuNPs was characterized by using UV-Vis, fluorescence, high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) and thermogravimetric (TGA) analysis. The surface plasmon resonance (SPR) band at 585 nm confirmed the reduction of auric chloride to AuNPs. The crystalline nature of the biosynthesized AuNPs was confirmed from the HRTEM images, XRD and selected area electron diffraction (SAED) pattern. The HRTEM images showed the mixture of triangular and spherical-like AuNPs having size between 5 and 20 nm. The weight loss of the AuNPs was measured by TGA as a function of temperature under a controlled atmosphere. The biomolecules are responsible for the reduction of AuCl4- ions and the formation of stable AuNPs which was confirmed by FTIR measurement. The synthesized AuNPs showed an excellent antibacterial activity against Candida albicans (ATCC 90028), Aspergillus flavus (ATCC 10124), Staphylococcus aureus (ATCC 25175), Salmonella typhi (ATCC 14028) and Vibrio cholerae (ATCC 14033). The minimum inhibitory concentration (MIC) of AuNPs was recorded against various microorganisms. Further, the synthesized AuNPs shows an excellent cytotoxic result against HeLa cancer cell lines at different concentrations.

  7. Photoscopic characterization of green synthesized silver nanoparticles from Trichosanthes tricuspidata and its antibacterial potential.

    PubMed

    Yuvarajan, Ragunathan; Natarajan, Devarajan; Ragavendran, Chinnasamy; Jayavel, Ramasamy

    2015-08-01

    The present study focused on the finding of reducing agents for the formation of silver nanoparticles (AgNPs) from the plant, Trichosanthes tricuspidata. The synthesized AgNPs were characterized using UV-Visible spectroscopy, particle size analyzer (PSA), X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) analyses. The UV-Visible spectrum resulted a sharp peak (at 430nm) represents the strong plasmon resonance of silver. The average size distributions of AgNPs were found to be 78.49nm, through (PSA), and the silver ion with its crystalline nature was confirmed using intensity (2θ) peak value of 38.22°, 44.66°, 64.61°, and 77.49°. The SEM micrograph revealed that the synthesized AgNPs have a spherical morphology with the size ranges from 20 to 28nm. AFM showed the presence of polydispersed AgNPs with its size (20 to 60nm in height). The gas chromatography-mass spectroscopy (GC-MS) study analyzed the responsible compounds present in the methanolic extracts for the bio-reduction of AgNPs and their antibacterial effect was studied. AgNPs exhibited preponderant activity than the methanolic extracts on clinical pathogens. Thus, the synthesized AgNPs might act as an effective antibacterial agent. Further studies are required to isolate the specific compound responsible for the reduction capability and its their inhibitory mechanisms for target bacterial strains. PMID:26044176

  8. The Effect of Green Synthesized CuO Nanoparticles on Callogenesis and Regeneration of Oryza sativa L.

    PubMed Central

    Anwaar, Sadaf; Maqbool, Qaisar; Jabeen, Nyla; Nazar, Mudassar; Abbas, Fazal; Nawaz, Bushra; Hussain, Talib; Hussain, Syed Z.

    2016-01-01

    In this study, we have investigated the effect of copper oxide nanoparticles (CuO-NPs) on callogenesis and regeneration of Oryza sativa L (Super Basmati, Basmati 2000, Basmati 370, and Basmati 385). In this regard, CuO-NPs have been bio-synthesized via Azadirachta indica leaf extract. Scanning electron microscope (SEM) analysis depicts average particle size of 40 ± 5 nm with highly homogenous and spherical morphology. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) have been employed to confirm the phase purity of the synthesized NPs. It is found that CuO-NPs exhibit very promising results against callus induction. It is attributed to the fact that green synthesized CuO-NPs at optimum dosage possess very supportive effects on plant growth parameters. In contrast to callogenesis, differential regeneration pattern has been observed against all of the examined O. sativa L. indigenous verities. Overall observation concludes that CuO, being one of the essential plant nutrients, has greatly tailored the nutritive properties at nano-scale.

  9. Characterization of Nano-Hydroxyapatite Synthesized from Sea Shells Through Wet Chemical Method

    NASA Astrophysics Data System (ADS)

    Santhosh, S.; Prabu, S. Balasivanandha

    2012-10-01

    Nano-hydroxyapatite (HA) was synthesized by a wet chemical reaction using powdered sea shells (CaO) as starting material which was converted to calcium hydroxide (Ca(OH)2) and subsequently reacted with phosphoric acid (H3PO4). Initially raw sea shells (CaCO3) were thermally converted to amorphous calcium oxide by heat treatment. Two sets of experiments were done; in the first experiment, HA powder was dried in an electric furnace and in the second experiment, the reactants were irradiated in a domestic microwave oven followed by microwave drying. In each set of experiments, the concentrations of the reactants were decreased gradually. HA was synthesized by slow addition of phosphoric acid (H3PO4) in to calcium hydroxide (Ca(OH)2) maintaining the pH of the solution at 10 to avoid the formation of calcium deficient apatites. In both the experiments, Ca:P ratio of 1.67 was maintained for the reagents. The synthesized samples showed X-ray diffraction (XRD) patterns corresponding to hydroxyapatite. The wet chemical process with furnace drying resulted in HA particles of size 7-34 nm, whereas microwave irradiated process yielded HA particles of size 34-102 nm as evidenced from XRD analyses. The above experimental work done by wet chemical synthesis to produce HA powder from sea shells is a simple processing method at room temperature. Microwave irradiation leads to uniform crystallite sizes as evident from this study, at differing concentrations of the reactants and is a comparatively easy method to synthesize HA. The high resolution scanning electron microscopy (HRSEM)/transmission electron microscopic (TEM) analyses revealed the characteristic rod-shaped nanoparticles of HA for the present study.

  10. Studies on magnetic properties of chemically synthesized crystalline calcium ferrite nanoparticles

    NASA Astrophysics Data System (ADS)

    Debnath, A.; Bera, A.; Chattopadhyay, K. K.; Saha, B.

    2016-05-01

    Spinel-type ferrites have taken a very important role for modern electronic industry. Most of these ferrites exhibit low-loss dielectric properties, high resistivity, low eddy current and also high temperature ferromagnetism. Calcium ferrite is one such important metal oxide which is environmentally safe, chemically stable, low cost and greatly abundant. This outstanding material of calcium ferrite is synthesized by a simple chemical precipitation method using NaOH as the precipitating agent. Ferric chloride anhydrous (FeCl3) and Calcium chloride dihydrate (CaCl2.2H2O) were used as iron and calcium sources respectively. The samples were heated at 200°C for 8h to obtain homogeneous powder of Calcium ferrite. The powders were characterized by using X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), Transmission electrical microscopy (TEM), and Fourier transform infrared spectroscopic (FTIR) measurements. The polycrystalline nature of the sample was confirmed by X-ray diffraction study. The magnetic properties of the sample were investigated by vibrating sample magnetometer (VSM) measurements. Magnetization curve of the prepared sample depicts that as synthesized calcium ferrite nanoparticles have saturation magnetic moment of 1.74 emu/g and the coercivity of 35.08 Oe with superparamagnetic behavior. The synthesized calcium ferrite nanoparticles with such magnetic properties will be a candidate material for different applications in electronics and exploring its functionality in the field of recently developing semiconductor device physics and spintronics.

  11. A chemical study of individual green glasses and brown glasses from 15426 - Implications for their petrogenesis

    NASA Technical Reports Server (NTRS)

    Ma, M.-S.; Liu, Y.-G.; Schmitt, R. A.

    1982-01-01

    Systematic chemical analyses of individual Apollo 15 green glasses were performed in order to: (1) study chemical variations among them; (2) understand their petrogenesis and source region; and (3) study their possible relationships with mare basalts in general. Brown glasses were also analyzed in order to study their chemical variations and their petrogenetic relationships to green glasses and mare basalts. The chemical composition of green and brown glasses is shown and variation diagrams of Sc, Cr2O3, FeO, and Co abundances in green glasses are presented. Igneous fractionation, two component magma mixing, and partial melting of heterogeneous source materials are alternate scenarios to explain strong observed correlations. The composition of green glasses indicates that they were derived by partial melting of the fractionated cumulate source materials formed from a magma ocean which had experienced certain degrees of olivine and plagioclase fractional crystallization.

  12. The scalability in the mechanochemical syntheses of edge functionalized graphene materials and biomass-derived chemicals.

    PubMed

    Blair, Richard G; Chagoya, Katerina; Biltek, Scott; Jackson, Steven; Sinclair, Ashlyn; Taraboletti, Alexandra; Restrepo, David T

    2014-01-01

    Mechanochemical approaches to chemical synthesis offer the promise of improved yields, new reaction pathways and greener syntheses. Scaling these syntheses is a crucial step toward realizing a commercially viable process. Although much work has been performed on laboratory-scale investigations little has been done to move these approaches toward industrially relevant scales. Moving reactions from shaker-type mills and planetary-type mills to scalable solutions can present a challenge. We have investigated scalability through discrete element models, thermal monitoring and reactor design. We have found that impact forces and macroscopic mixing are important factors in implementing a truly scalable process. These observations have allowed us to scale reactions from a few grams to several hundred grams and we have successfully implemented scalable solutions for the mechanocatalytic conversion of cellulose to value-added compounds and the synthesis of edge functionalized graphene. PMID:25407922

  13. Liquid Gallium based temperature sensitive functional fluid dispersing chemically synthesized FeMB nanoparticles

    NASA Astrophysics Data System (ADS)

    Park, H. S.; Cao, L. F.; Dodbiba, G.; Fujita, T.

    2009-02-01

    In this work, FeMB (M = Nb, V) nanoparticles were first reported to be synthesized by a chemical method, from reduction of FeCl2, NbF5 (and NH4VO3) using NaBH4 as a reducing agent in aqueous solution. A new temperature sensitive functional fluid was then prepared by dispersing silica coated FeNbVB nanoparticles in liquid gallium. The result shows that the FeNbVB nanoparticles exhibit an oxidation resistance better than that of FeNbB nanoparticles. The FeNbVB nanoparticles were in the size range of 30 - 50 nm and the thickness of silica layer was observed about 10 nm by means of transmission electron microscopy. The magnetization of the synthesized particles and fluid shows a temperature dependency within the testing temperature range of 293 - 353 K, which indicated their application potential in magneto-caloric energy conversion devices.

  14. Antimicrobial fabrication of cotton fabric and leather using green-synthesized nanosilver.

    PubMed

    Velmurugan, Palanivel; Cho, Min; Lee, Sang-Myeong; Park, Jung-Hee; Bae, Sunyoung; Oh, Byung-Taek

    2014-06-15

    This study aims to investigate the green synthesis of silver nanoparticles (AgNPs) by Erigeron annuus (L.) pers flower extract as reducing and capping agent, and evaluation of their antibacterial activities for the first time. The obtained product was confirmed by UV-Vis spectrum, high resolution-transmission electron microscopy, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction studies. The optimum AgNPs production was achieved at pH 7, metal silver (Ag(+) ion) concentration of 2.0mM, flower extract concentration 4%, and time 335 min. In addition, the antibacterial activity of cotton fabrics and tanned leather loaded with AgNPs, commercial AgNPs, flower extract, Ag(+) ion and blend of flower extract with AgNPs were evaluated against Gram-positive odor causing bacteria Brevibacterium linens and Staphylococcus epidermidis. The results showed maximum zone of inhibition (ZOI) by the cotton fabrics embedded with blend of flower extract and AgNPs against B. linens. The structure and morphology of cotton fabric and leather samples embedded with AgNPs, Ag(+) ion and blend of flower extract with AgNPs were examined under field emission scanning electron microscope. PMID:24721085

  15. Efficacy of larvicidal activity of green synthesized titanium dioxide nanoparticles using Mangifera indica extract against blood-feeding parasites.

    PubMed

    Rajakumar, Govindasamy; Rahuman, Abdul Abdul; Roopan, Selvaraj Mohana; Chung, Ill-Min; Anbarasan, Karunanithi; Karthikeyan, Viswanathan

    2015-02-01

    Titanium dioxide nanoparticles (TiO2 NPs) are considered to be among the best photocatalytic materials due to their long-term thermodynamic stability, strong oxidizing power, and relative non-toxicity. Nano-preparations with TiO2 NPs are currently under investigation as novel treatments for acne vulgaris, recurrent condyloma acuminata, atopic dermatitis, hyperpigmented skin lesions, and other non-dermatologic diseases. The present study was to investigate the acaricidal and larvicidal activity of synthesized TiO2 NPs utilizing leaf aqueous extract of Mangifera indica L. (Anacardiaceae) against hematophagous parasites. The anti-parasitic activity of TiO2 NPs against the larvae of Rhipicephalus (Boophilus) microplus, Hyalomma anatolicum anatolicum and Haemaphysalis bispinosa (Acari: Ixodidae), fourth instar larvae of Anopheles subpictus, and Culex quinquefasciatus (Diptera: Culicidae) were assessed. The green synthesized TiO2 NPs were analyzed by UV-Vis, FTIR, X-ray diffraction (XRD), AFM, SEM, and TEM. The XRD analysis of synthesized TiO2 NPs revealed the dominant peak at 2θ value of 27.81 which matched the 110 crystallographic plane of the rutile structure indicating the crystal structure. The FTIR spectra exhibited a prominent peak at 3,448 cm(-1) and showed OH stretching due to the alcoholic group, and the OH group may act as a capping agent. The SEM images of TiO2 NPs displayed spherical, oval in shape, individual, and some in aggregates. Characterization of the synthesized TiO2 NPs using AFM offered three-dimensional visualization and uneven surface morphology. The TEM micrograph showed agglomerates, round and slight elongation with an average size of 30 ± 5 nm. The maximum efficacy was observed in synthesized TiO2 NPs against the larvae of R. microplus, Hyalomma anatolicum anatolicum, Haemaphysalis bispinosa, A. subpictus, and Culex quinquefasciatus with LC50 value of 28.56, 33.17, 23.81, 5.84, and 4.34 mg/L, respectively. In the present study, a novel

  16. Interaction Studies of Greenly Synthesized Gold Nanoparticles with Bovine Serum Albumin (BSA) Using Fluorescence Spectroscopy.

    PubMed

    Ravikumar, Sambandam; Sreekanth, T V M; Eom, In-Yong

    2015-12-01

    In the present study, gold nanoparticles (AuNPs) with an average particle size of -41.23 nm were synthesized using eco-friendly reducing material (i.e., aqueous Nelumbo nucifera root extract). Rapid reduction results in the formation of polydispersed nanoparticles. The formation of AuNPs was characterized by surface plasmon resonance (SPR) which was determined by UV-Vis spectra (band at 544 nm), FTIR, SEM-EDX, TEM, HR-TEM, and XRD. This study aims to investigate the interaction between AuNPs and Bovine Serum Albumin (BSA) using fluorescence spectroscopy. The analysis of fluorescence spectra and intensity at physiological pH in an aqueous solution indicates that AuNPs have a potent ability to quench the BSA fluorescence by both quenching mechanisms. Resonance light scattering spectra indicated the formation of BSA-AuNPs complex. The number of binding sites and binding constants were determined based on fluorescence quenching at different temperatures. The thermodynamic parameters were also calculated at various temperatures that indicate that hydrophobic forces are abundant in the AuNPs-BSA complex. Negative ΔG degrees values suggest that the binding process is spontaneous. Synchronous fluorescence spectra showed a blue shift and CD spectra showed an increase in a-helicity content which is an indication of increasing hydrophobicity. PMID:26682387

  17. Antibacterial and DNA degradation potential of silver nanoparticles synthesized via green route.

    PubMed

    Manna, Dilip K; Mandal, Amit K; Sen, Ipsita K; Maji, Praloy K; Chakraborti, Soumyananda; Chakraborty, Ranadhir; Islam, Syed S

    2015-09-01

    Silver nanoparticles (AgNPs) were synthesized using a hetero polysaccharide (PS) isolated from Lentinus squarrosulus (Mont.) Singer. The polysaccharide fraction (consisting of glucose, fucose and galactose) serves the role of both reducing as well as stabilizing agent. UV-vis spectroscopy showed maximum absorbance at 407 nm due to surface plasmon resonance. High resolution transmission electron microscopy (HRTEM) exhibited that the average diameter of the nanoparticles was 2.78±1.47 nm. The XRD analysis revealed face-centered cubic (fcc) geometry of silver nanoparticles. Antibacterial activity of the AgNPs-PS conjugate was tested against multiple antibiotics resistant (MAR) Escherichia coli strain MREC33 and found that the killing was due to generation of reactive oxygen species (ROS). Internalization of AgNPs-PS conjugate along with its DNA degradation capability was demonstrated using flow cytometry. AgNPs-PS conjugates showed negligible toxicity to human RBCs. This LD50 dosage of AgNPs-PS conjugates in combination with each of the four antibiotics (ampicillin, azithromycin, kanamycin and netilmicin) to which E. coli MREC33 was resistant, showed synergistic effect to inhibit complete bacterial growth. PMID:26188293

  18. Reflectance and minority carrier lifetime of silicon nanoholes synthesized by chemical etching method

    NASA Astrophysics Data System (ADS)

    Zhang, Daisheng; Jia, Rui; Chen, Chen; Ding, Wuchang; Jin, Zhi; Liu, Xinyu; Ye, Tianchun

    2014-05-01

    Silicon nanoholes (Si NHs) were synthesized by a simple metal-assisted chemical etching method. With different pre-etching time of Ag particles, Si NHs with different morphology and Si nanowires (NWs) were prepared. After tetramethyl ammonium hydroxide (TMAH) etching, the NH sample with pre-etching Ag particles for 20 min show average reflectance below 5% which is comparable to the reflectance of the NW sample. The minority carrier lifetime of this NH sample is 58.2 μs due to their low surface recombination, while the lifetime of the NWs is 38.0 μs under the same iodine-ethanol passivation.

  19. Electrical conductivity of single CdS nanowire synthesized by aqueous chemical growth

    NASA Astrophysics Data System (ADS)

    Long, Yunze; Chen, Zhaojia; Wang, Wenlong; Bai, Fenglian; Jin, Aizi; Gu, Changzhi

    2005-04-01

    In this Letter, we report on the temperature-dependent conductivity and current-voltage curve of a single CdS nanowire, which was synthesized by a simple aqueous chemical growth method. A pair of platinum microleads was fabricated on the single CdS nanowire by focused ion-beam deposition. The room-temperature conductivity and the band gap of the single CdS wire are 0.82Ω-1cm-1 and 0.055eV, respectively. When the applied electric field is larger than 1090Vcm-1, the CdS nanowire shows a nonlinear I-V curve at room temperature.

  20. Investigation of quantum confinement behavior of zinc sulphide quantum dots synthesized via various chemical methods

    SciTech Connect

    Jose, Meera Sakthivel, T. Chandran, Hrisheekesh T. Nivea, R. Gunasekaran, V.

    2014-10-15

    In this work, undoped and Ag-doped ZnS quantum dots were synthesized using various chemical methods. The products were characterized using X-ray diffraction (XRD), UV-visible spectroscopy and Photoluminescence spectroscopy. Our results revealed that the size of the as-prepared samples range from 1–6 nm in diameter and have a cubic zinc-blende structure. Also, we observed the emission of different wavelength of light from different sized quantum dots of the same material due to quantum confinement effect. The results will be presented in detail and ZnS can be a potential candidate for optical device development and applications.

  1. Wet-Chemically Synthesized Colloidal Semiconductor Nanostructures as Optical Gain Media.

    PubMed

    Ong, Xuanwei; Zhi, Min; Gupta, Shashank; Chan, Yinthai

    2016-03-01

    An overview on the development of wet-chemically synthesized semiconductor nanostructures as optical gain materials is presented in this Review, beginning with the first demonstration of amplified spontaneous emission in zero-dimensional quantum dots and evolving to more sophisticated heterostructures such as one-dimensional core-seeded nanorods, branched core-seeded tetrapods and two-dimensional nanoplatelets. The advantages and challenges of utilizing strongly quantum-confined colloidal semiconductor materials as gain media are discussed, and a concerted effort is made to elaborate on how the progression towards more structurally complex architectures has allowed for dramatic improvements in performance and stability over the archetypal quantum dot. PMID:26822201

  2. A new green chemistry method based on plant extracts to synthesize gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Montes Castillo, Milka Odemariz

    Extraordinary chemical and physical properties exhibited by nanomaterials, as compared to their bulk counterparts, have made the area of nanotechnology a growing realm in the past three decades. It is the nanoscale size (from 1 to 100 nm) and the morphologies of nanomaterials that provide several properties and applications not possible for the same material in the bulk. Magnetic and optical properties, as well as surface reactivity are highly dependent on the size and morphology of the nanomaterial. Diverse nanomaterials are being widely used in molecular diagnostics as well as in medicine, electronic and optical devices. Among the most studied nanomaterials, gold nanoparticles are of special interest due to their multifunctional capabilities. For instance, spherical gold nanoparticles measuring 15-20 nm in diameter have been studied due to their insulin binding properties. Also, thiol functionalized gold nanoparticles between 5 and 30 nm are used in the detection of DNA. Thus, harnessing the shape and size of gold nanoparticles plays an important role in science and technology. The synthesis of gold nanoparticles via the reduction of gold salts, using citrate or other reducing agents, has been widely studied. In recent years, algae, fungi, bacteria, and living plants have been used to reduce trivalent gold (Au3+) to its zero oxidation state (Au 0) forming gold nanoparticles of different sizes and shapes. In addition, plant biomasses have also been studied for their gold-reducing power and nanoparticle formation. Although there is information about the synthesis of the gold nanoparticles by biologically based materials; to our knowledge, the study of the use of alfalfa extracts has not been reported. This innovation represents a significant improvement; that is an environmentally friendly method that does not use toxic chemicals. Also, the problem of extracting the formed gold nanoparticles from biomaterials is addressed in this research but still remains to be

  3. A 'Fine' chemical industry for life science products: green solutions to chemical challenges.

    PubMed

    Bruggink, A; Straathof, A J J; van der Wielen, L A M

    2003-01-01

    Modern biotechnology, in combination with chemistry and process technology, is crucial for the development of new clean and cost effective manufacturing concepts for fine-chemical, food specialty and pharmaceutical products. The impact of biocatalysis on the fine-chemicals industry is presented, where reduction of process development time, the number of reaction steps and the amount of waste generated per kg of end product are the main targets. Integration of biosynthesis and organic chemistry is seen as a key development. The advances in bioseparation technology need to keep pace with the rate of development of novel bio- or chemocatalytic process routes with revised demands on process technology. The need for novel integrated reactors is also presented. The necessary acceleration of process development and reduction of the time-to-market seem well possible, particularly by integrating high-speed experimental techniques and predictive modelling tools. This is crucial for the development of a more sustainable fine-chemicals industry. The evolution of novel 'green' production routes for semi-synthetic antibiotics (SSAs) that are replacing existing chemical processes serves as a recent and relevant case study of this ongoing integration of disciplines. We will also show some challenges in this specific field. PMID:12747542

  4. Electronic Properties of Large-scale Graphene Chemical Vapor Synthesized on Nickel and on Sapphire

    NASA Astrophysics Data System (ADS)

    Cao, Helin; Zhang, Liyuan; Chen, Yong; Yu, Qingkai; Li, Hao

    2009-03-01

    We have studied the electronic transport properties of large area few-layer graphene/graphitic films grown by two different chemical vapor based methods. The first type of samples (metal-transfer graphene) is synthesized by carbon segregation from Ni, then transferred to SiO2/Si substrates. The second type of samples is synthesized by direct chemical vapor deposition (CVD) on sapphire. We measured these samples under variable temperatures (from 2K to 300 K) and transverse magnet fields (from 0 to 7 T). For both types of samples, we found a negative magnetoresistance at low field, and carrier mobilities on the order of several hundreds of cm^2/V-s. For metal-transfer graphene in particular, we were able to measure a moderate field effect response, using the highly doped Si substrate as back gate. The observed magnetoresistance shows characteristic features of weak localization, from which we extract various carrier scattering lengths in the metal-transfer graphene samples. Comparison with those measured in mechanically exfoliated graphene suggests possibly different carrier scattering mechanisms for graphene materials prepared with different methods.

  5. A comparative study on biologically and chemically synthesized silver nanoparticles induced Heat Shock Proteins on fresh water fish Oreochromis niloticus.

    PubMed

    Girilal, M; Krishnakumar, V; Poornima, Paramasivan; Mohammed Fayaz, A; Kalaichelvan, P T

    2015-11-01

    The wide applicability of silver nanoparticles in medicine and pharmaceutical industries leads to its over exploitation and thus contaminating our environment. Majority of these nanoscale dimension particles finally accumulates in fresh water and marine ecosystem. As the nanoparticles behave entirely different from its corresponding bulk material, a better understanding of their environmental impacts in aquatic ecosystems is inevitable. The study was focused on a comparative stress physiology analysis of chemically synthesized silver nanoparticles and biogenic silver nanoparticles. Half maximal inhibitory concentration of biologically synthesized and chemically synthesized nanoparticles was found out (30μg/mL and 20μg/mL respectively). The Heat Shock Protein (HSP70) secretion was analysed in the fresh water fish Oreochromis niloticus after exposing to different concentrations of biologically and chemically synthesized silver nanoparticles along with the silver in its ionic form. The intense immune-histochemical staining of fish tissues (muscle, kidney and liver) analyzed proportionately reflected the stress created. The colour intensity was directly proportional to the stress created or the stress protein released. High level of HSP70 expression was observed in all of the fish tissues exposed to silver ions and chemically synthesized silver nanoparticles, when compared to that of biologically synthesized. The results revealed the significance of comparatively safe and less toxic biogenic nanoparticles compared to the chemically synthesized. PMID:26291676

  6. Versatility of chemically synthesized guide RNAs for CRISPR-Cas9 genome editing.

    PubMed

    Kelley, Melissa L; Strezoska, Žaklina; He, Kaizhang; Vermeulen, Annaleen; Smith, Anja van Brabant

    2016-09-10

    The CRISPR-Cas9 system has become the most popular and efficient method for genome engineering in mammalian cells. The Streptococcus pyogenes Cas9 nuclease can function with two types of guide RNAs: the native dual crRNA and tracrRNA (crRNA:tracrRNA) or a chimeric single guide RNA (sgRNA). Although sgRNAs expressed from a DNA vector are predominant in the literature, guide RNAs can be rapidly generated by chemical synthesis and provide equivalent functionality in gene editing experiments. This review highlights the attributes and advantages of chemically synthesized guide RNAs including the incorporation of chemical modifications to enhance gene editing efficiencies in certain applications. The use of synthetic guide RNAs is also uniquely suited to genome-scale high throughput arrayed screening, particularly when using complex phenotypic assays for functional genomics studies. Finally, the use of synthetic guide RNAs along with DNA-free sources of Cas9 (mRNA or protein) allows for transient CRISPR-Cas9 presence in the cell, thereby resulting in a decreased probability of off-target events. PMID:27374403

  7. Biobased chemicals: the convergence of green chemistry with industrial biotechnology.

    PubMed

    Philp, Jim C; Ritchie, Rachael J; Allan, Jacqueline E M

    2013-04-01

    Policy issues around biobased chemicals are similar to those for biobased plastics. However, there are significant differences that arise from differences in production volumes and the more specific applications of most chemicals. The drivers for biobased chemicals production are similar to those for biobased plastics, particularly the environmental drivers. However, in Europe, biobased chemical production is further driven by the need to improve the competitiveness of the chemicals industry. PMID:23394962

  8. Effects of green-synthesized silver nanoparticles on lung cancer cells in vitro and grown as xenograft tumors in vivo

    PubMed Central

    He, Yan; Du, Zhiyun; Ma, Shijing; Liu, Yue; Li, Dongli; Huang, Huarong; Jiang, Sen; Cheng, Shupeng; Wu, Wenjing; Zhang, Kun; Zheng, Xi

    2016-01-01

    Silver nanoparticles (AgNPs) have now been recognized as promising therapeutic molecules and are extending their use in cancer diagnosis and therapy. This study demonstrates for the first time the antitumor activity of green-synthesized AgNPs against lung cancer in vitro and in vivo. Cytotoxicity effect was explored on human lung cancer H1299 cells in vitro by MTT and trypan blue assays. Apoptosis was measured by morphological assessment, and nuclear factor-κB (NF-κB) transcriptional activity was determined by a luciferase reporter gene assay. The expressions of phosphorylated stat3, bcl-2, survivin, and caspase-3 were examined by Western blot analysis. AgNPs showed dose-dependent cytotoxicity and stimulation of apoptosis in H1299 cells. The effects on H1299 cells correlated well with the inhibition of NF-κB activity, a decrease in bcl-2, and an increase in caspase-3 and survivin expression. AgNPs significantly suppressed the H1299 tumor growth in a xenograft severe combined immunodeficient (SCID) mouse model. The results demonstrate the anticancer activities of AgNPs, suggesting that they may act as potential beneficial molecules in lung cancer chemoprevention and chemotherapy, especially for early-stage intervention. PMID:27217750

  9. Environmental Chemistry and Chemical Ecology of "Green Tide" Seaweed Blooms.

    PubMed

    Van Alstyne, Kathryn L; Nelson, Timothy A; Ridgway, Richard L

    2015-09-01

    Green tides are large growths or accumulations of green seaweeds that have been increasing in magnitude and frequency around the world. Because green tides consist of vast biomasses of algae in a limited area and are often seasonal or episodic, they go through periods of rapid growth in which they take up large amounts of nutrients and dissolved gases and generate bioactive natural products that may be stored in the plants, released into the environment, or broken down during decomposition. As a result of the use and production of inorganic and organic compounds, the algae in these blooms can have detrimental impacts on other organisms. Here, we review some of the effects that green tides have on the chemistry of seawater and the effects of the natural products that they produce. As blooms are developing and expanding, algae in green tides take up inorganic nutrients, such as nitrate and ortho-phosphate, which can limit their availability to other photosynthetic organisms. Their uptake of dissolved inorganic carbon for use in photosynthesis can cause localized spikes in the pH of seawater during the day with concomitant drops in the pH at night when the algae are respiring. Many of the algae that form green-tide blooms produce allelopathic compounds, which are metabolites that affect other species. The best documented allelopathic compounds include dimethylsulfoniopropionate (DMSP), dopamine, and reactive oxygen species (ROS) and their breakdown products. DMSP and dopamine are involved in defenses against herbivores. Dopamine and ROS are released into seawater where they can be allelopathic or toxic to other organisms. Thus, these macroalgal blooms can have harmful effects on nearby organisms by altering concentrations of nutrients and dissolved gas in seawater and by producing and releasing allelopathic or toxic compounds. PMID:25972565

  10. [Studies on photo-electron-chemical catalytic degradation of the malachite green].

    PubMed

    Li, Ming-yu; Diao, Zeng-hui; Song, Lin; Wang, Xin-le; Zhang, Yuan-ming

    2010-07-01

    A novel two-compartment photo-electro-chemical catalytic reactor was designed. The TiO2/Ti thin film electrode thermally formed was used as photo-anode, and graphite as cathode and a saturated calomel electrode (SCE) as the reference electrode in the reactor. The anode compartment and cathode compartment were connected with the ionic exchange membrane in this reactor. Effects of initial pH, initial concentration of malachite green and connective modes between the anode compartment and cathode compartment on the decolorization efficiency of malachite green were investigated. The degradation dynamics of malachite green was studied. Based on the change of UV-visible light spectrum, the degradation process of malachite green was discussed. The experimental results showed that, during the time of 120 min, the decolouring ratio of the malachite green was 97.7% when initial concentration of malachite green is 30 mg x L(-1) and initial pH is 3.0. The catalytic degradation of malachite green was a pseudo-first order reaction. In the degradation process of malachite green the azo bond cleavage and the conjugated system of malachite green were attacked by hydroxyl radical. Simultaneity, the aromatic ring was oxidized. Finally, malachite green was degraded into other small molecular compounds. PMID:20825023

  11. Chemical composition of the green alga Codium Divaricatum Holmes.

    PubMed

    He, Zhizhou; Zhang, Anjiang; Ding, Lisheng; Lei, Xinxiang; Sun, Jianzhang; Zhang, Lixue

    2010-12-01

    A new sterol, 24-R-stigmasta-4,25-diene-3β,6β-diol (1), along with three known compounds (2-3), was isolated from the green alga Codium divaricatum Holmes, a traditional Chinese medicine, which is efficacious against cancer. All structures were determined by spectroscopic methods and comparison with related known compounds. Single-crystal X-ray crystallography allowed us to confirm the structure of 1. To our knowledge, the compound 1 is reported as the first from natural source, and compounds 2, 4 have not been isolated from green algae before. PMID:20655992

  12. Physico-chemical studies of amorphous carbon nanotubes synthesized at low temperature

    SciTech Connect

    Tan, Kim Han; Ahmad, Roslina; Leo, Bey Fen; Yew, Ming Chian; Ang, Bee Chin; Johan, Mohd Rafie

    2012-08-15

    Highlights: ► Amorphous carbon nanotubes are successfully produced via a simple method at low temperature. ► Nanotubes in straight morphologies with open ends. ► Acid treatment increases the extent of amorphous for nanotubes. ► Amorphous nanotubes exhibit phenomena of π plasmon absorbance and possess higher bandgap. -- Abstract: This work provides better understanding on the nature of amorphous carbon nanotubes, which are synthesized via a simple chemical route. Amorphous carbon nanotubes (α-CNTs) are successfully synthesized by heating a mixture of ferrocene and ammonium chloride at temperature as low as 200 °C and are treated with hydrochloric acid. Transmission and field emission scanning electron microscopy techniques are performed to examine the morphology and dimension of the samples. X-ray diffraction tests confirm the amorphous structure of the nanotubes. The Fourier transform infrared spectroscopy and Raman studies indicate that the treated α-CNTs consist of many defective walls and are more amorphous compared with the untreated α-CNTs. Ultraviolet–visible absorption studies reveal that the untreated and treated α-CNTs exhibit plasmon absorbance with high bandgaps of 4 eV and 4.35 eV, respectively.

  13. Electrical properties of boron-doped MWNTs synthesized by hot-filament chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Ishii, S.; Nagao, M.; Watanabe, T.; Tsuda, S.; Yamaguchi, T.; Takano, Y.

    2009-10-01

    We have synthesized a large amount of boron-doped multiwalled carbon nanotubes (MWNTs) by hot-filament chemical vapor deposition. The synthesis was carried out in a flask using a methanol solution of boric acid as a source material. The scanning electron microscopy, transmission electron microscopy, and micro-Raman spectroscopy were performed to evaluate the structural properties of the obtained MWNTs. In order to evaluate the electrical properties, temperature dependence of resistivity was measured in an individual MWNTs with four metal electrodes. The Raman shifts suggest carrier injection into the boron-doped MWNTs, but the resistivity of the MWNTs was high and increased strongly with decreasing temperature. Defects induced by the plasma may cause this enhanced resistivity.

  14. Optical and structural studies of ZnS nanoparticles synthesized via chemical in situ technique

    NASA Astrophysics Data System (ADS)

    Mamiyev, Zamin Q.; Balayeva, Narmina O.

    2016-02-01

    ZnS nanoparticles (NPs) have been synthesized by the facile chemical route with a narrow size distribution in the MA/octene-1 copolymer matrix and effect of reaction time has been discussed. X-ray diffraction pattern confirms the pure cubic phase of ZnS with 5-7 nm average crystal sizes which are in good agreement with the AFM and UV-vis measurements. Absorption spectra exhibit a strong blue shift from the bulk with the 3.98 eV optical band gap which clearly indicates the strong size confinement effect. Thermogravimetric analyses show increased thermal stability of the nanocomposite compared to the copolymer. The possible growth mechanism of the particles formation and stabilization has been discussed.

  15. 3D SERS Imaging Using Chemically Synthesized Highly Symmetric Nanoporous Silver Microparticles.

    PubMed

    Vantasin, Sanpon; Ji, Wei; Tanaka, Yoshito; Kitahama, Yasutaka; Wang, Mengfan; Wongravee, Kanet; Gatemala, Harnchana; Ekgasit, Sanong; Ozaki, Yukihiro

    2016-07-11

    3D surface-enhanced Raman scattering (SERS) imaging with highly symmetric 3D silver microparticles as a SERS substrate was developed. Although the synthesis method is purely chemical and does not involve lithography, the synthesized nanoporous silver microparticles possess a regular hexapod shape and octahedral symmetry. By using p-aminothiophenol (PATP) as a probe molecule, the 3D enhancement patterns of the particles were shown to be very regular and predictable, resembling the particle shape and exhibiting symmetry. An application to the detection of 3D inhomogeneity in a polymer blend, which relies on the predictable enhancement pattern of the substrate, is presented. 3D SERS imaging using the substrate also provides an improvement in spatial resolution along the Z axis, which is a challenge for Raman measurement in polymers, especially layered polymeric systems. PMID:27240138

  16. Spectacular enhancement of thermoelectric phenomena in chemically synthesized graphene nanoribbons with substitution atoms.

    PubMed

    Zberecki, K; Swirkowicz, R; Wierzbicki, M; Barnaś, J

    2016-07-21

    We analyze theoretically the transport and thermoelectric properties of graphene nanoribbons of a specific geometry, which have been synthesized recently from polymers [Cai, et al., Nature, 2011, 466, 470]. When such nanoribbons are modified at one of the two edges by Al or N substitutions, they acquire a ferromagnetic moment localized at the modified edge. We present numerical results on the electronic structure and thermoelectric properties (including also spin thermoelectricity) of the modified nanoribbons. The results show that such nanoribbons can display large thermoelectric efficiency in certain regions of chemical potential, where the corresponding electric and spin figures of merit achieve unusually large values. The enhancement of thermoelectric efficiency follows from a reduced phonon heat conductance of the nanoribbons and from their peculiar electronic band structure. Thus, such nanoribbons are promising for practical applications in nanoelectronic and spintronic devices. PMID:27331357

  17. Photoluminescence of Ag-doped ZnSe nanowires synthesized by metalorganic chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Zhang, X. T.; Ip, K. M.; Li, Quan; Hark, S. K.

    2005-05-01

    Photoluminescence of Ag-doped ZnSe nanowires synthesized by metalorganic chemical vapor deposition is investigated in the temperature range from 10to300K. Ag impurities were introduced into the ZnSe nanowires during the growing process. Some dominating Ag-related centers are found. Especially, the strong zero-phonon bound exciton luminescence with energy near 2.747eV is attributed to a neutral AgZn acceptor complex. This is because the emission peak at the same energy is observed only in the photoluminescence spectrum of the Ag-doped bulk ZnSe. A new luminescence peak at 2.842eV is attributed to the recombination of excitons bound to ionized acceptors (I2h) in the hexagonal phase of ZnSe nanowires. The physical origins of the emissions are briefly discussed.

  18. Carbon impurities on graphene synthesized by chemical vapor deposition on platinum

    SciTech Connect

    Ping, Jinglei; Fuhrer, Michael S.

    2014-07-28

    We report nanocrystalline carbon impurities coexisting with graphene synthesized via chemical vapor deposition on platinum. For certain growth conditions, we observe micron-size island-like impurity layers which can be mistaken for second graphene layers in optical microscopy or scanning electron microscopy. The island orientation depends on the crystalline orientation of the Pt, as shown by electron backscatter diffraction, indicating growth of carbon at the platinum surface below graphene. Dark-field transmission electron microscopy indicates that in addition to uniform single-crystal graphene, our sample is decorated with nanocrystalline carbon impurities with a spatially inhomogeneous distribution. The impurity concentration can be reduced significantly by lowering the growth temperature. Raman spectra show a large D peak, however, electrical characterization shows high mobility (∼8000 cm{sup 2}/Vs), indicating a limitation for Raman spectroscopy in characterizing the electronic quality of graphene.

  19. Experimental investigation of optical and magneto optical effects of chemically synthesized cobalt nanocolloids

    NASA Astrophysics Data System (ADS)

    Parakkal, Fasalurahman; Babukutty, Blessy; Azad Vettiyadan, Basiluddeen; Kalarikkal, Nandakumar; Nair, Swapna S.

    2016-04-01

    Surfactant coated (oleic acid) cobalt nanocolloids are synthesized using the chemical reduction technique. The colloidal cobalt particles are characterized by x-ray diffraction, transmission electron microscopy and a superconducting quantum interference device. Structural characterization of the samples confirms the formation of cobalt in fcc form. The magnetic field induced optical anisotropy is probed through Faraday rotation for both concentrated and diluted colloids. The magneto optical signals for different concentrations are analysed and it is observed that the behaviour can be fitted for a Langevin curve for diluted suspensions, while the deviation is higher for concentrated suspensions. Optical absorption spectra show quantum confinement of nanoparticles leading to a blue shift in the electronic energy band gap. The band gap varied from 2 eV to 4 eV showing semiconductor like behaviour.

  20. Electrical characterization of graphene films synthesized by low-temperature microwave plasma chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Okigawa, Yuki; Tsugawa, Kazuo; Yamada, Takatoshi; Ishihara, Masatou; Hasegawa, Masataka

    2013-10-01

    In this Letter, we discuss the results of Hall effect measurements to examine the electrical properties of the graphene films synthesized by low-temperature microwave plasma chemical vapor deposition. Van der Pauw devices with sizes of 50-100 μm were fabricated, for which we observed p-type conduction and mobility from 10 to 100 cm2/V s. To investigate the mobility dispersion, we performed Raman mapping to quantify the number of defects and the disorder in graphene films. The results suggest that the D-band/G-band intensity ratio is correlated with the mobility. Moreover, we discuss the factors controlling the mobility and how to improve the quality of the graphene films by reducing the number of defects.

  1. Room-Temperature Ferromagnetism in Chemically Synthesized Sn₁-xCox O₂ Powders

    SciTech Connect

    Punnoose, Alex; Hays, Jason S.; Gopal, Vidyut; Shutthanandan, V.

    2004-08-30

    Room temperature ferromagnetism is observed in chemically synthesized powder samples of Sn₁₋xCox O₂ with x = 0.005 and 0.01. Magnetic hysteresis loops are ovserved at 300K with coercivity Hc ~ 630 Oe, saturation magnetization Ms ~0.133μв and about 31% remenance. Analyses of the magnetization data of paramagnetic samples with x = 0.01 and 0.03, measured as a function of temperature (3-330K) and magnetic field (up to 50kOe), indicated the presence of Co²⁺ ions with spin S = 3/2. Magnetic data obtained from samples prepared at different temperatures indicate that the observed ferromagnetism for x ≤ 0.01 might have been triggered by changes in the oxygen stiochiometry.

  2. Characterization of ZnS thin films synthesized through a non-toxic precursors chemical bath

    SciTech Connect

    Rodríguez, C.A.; Sandoval-Paz, M.G.; Cabello, G.; Flores, M.; Fernández, H.; Carrasco, C.

    2014-12-15

    Highlights: • High quality ZnS thin films have been deposited by chemical bath deposition technique from a non-toxic precursor’s solution. • Nanocrystalline ZnS thin films with large band gap energy were synthesized without using ammonia. • Evidence that the growing of the thin films is carried out by means of hydroxide mechanism was found. • The properties of these ZnS thin films are similar and in some cases better than the corresponding ones produced using toxic precursors such as ammonia. - Abstract: In solar cells, ZnS window layer deposited by chemical bath technique can reach the highest conversion efficiency; however, precursors used in the process normally are materials highly volatile, toxic and harmful to the environment and health (typically ammonia and hydrazine). In this work the characterization of ZnS thin films deposited by chemical bath in a non-toxic alkaline solution is reported. The effect of deposition technique (growth in several times) on the properties of the ZnS thin film was studied. The films exhibited a high percentage of optical transmission (greater than 80%); as the deposition time increased a decreasing in the band gap values from 3.83 eV to 3.71 eV was observed. From chemical analysis, the presence of ZnS and Zn(OH){sub 2} was identified and X-ray diffraction patterns exhibited a clear peak corresponding to ZnS hexagonal phase (1 0 3) plane, which was confirmed by electron diffraction patterns. From morphological studies, compact samples with well-defined particles, low roughness, homogeneous and pinhole-free in the surface were observed. From obtained results, it is evident that deposits of ZnS–CBD using a non-toxic solution are suitable as window layer for TFSC.

  3. Induction of Apoptosis by Green Synthesized Gold Nanoparticles Through Activation of Caspase-3 and 9 in Human Cervical Cancer Cells

    PubMed Central

    Baharara, Javad; Ramezani, Tayebe; Divsalar, Adeleh; Mousavi, Marzieh; Seyedarabi, Arefeh

    2016-01-01

    Background: Gold Nanoparticles (GNPs) are used in imaging and molecular diagnostic applications. As the development of a novel approach in the green synthesis of metal nanoparticles is of great importance and a necessity, a simple and safe method for the synthesis of GNPs using plant extracts of Zataria multiflora leaves was applied in this study and the results on GNPs’ anticancer activity against HeLa cells were reported. Methods: The GNPs were characterized by UV-visible spectroscopy, FTIR, TEM, DLS and Zeta-potential measurements. In addition, the cellular up-take of nanoparticles was investigated using Dark Field Microscopy (DFM). Induction of apoptosis by high dose of GNPs in HeLa cells was assessed by MTT assay, Acridin orange, DAPI staining, Annexin V/PI double-labeling flow cytometry and caspase activity assay. Results: UV-visible spectroscopy results showed a surface plasmon resonance band for GNPs at 530 nm. FTIR results demonstrated an interaction between plant extract and nanoparticles. TEM images revealed different shapes for GNPs and DLS results indicated that the GNPs range in size from 10 to 42 nm. The Zeta potential values of the synthesized GNPs were between 30 to 50 Mev, indicating the formation of stable particles. As evidenced by MTT assay, GNPs inhibit proliferation of HeLa cells in dose-dependent GNPs and cytotoxicity of GNPs in Bone Marrow Mesenchymal Stem Cell (BMSCs) was lower than cancerous cells. At nontoxic concentrations, the cellular up-take of the nanoparticles took place. Acridin orange and DAPI staining showed morphological changes in the cell’s nucleus due to apoptosis. Finally, caspase activity assay demonstrated HeLa cell’s apoptosis through caspase activation. Conclusion: The results showed that GNPs have the ability to induce apoptosis in HeLa cells. PMID:27141266

  4. Amelioration of excision wounds by topical application of green synthesized, formulated silver and gold nanoparticles in albino Wistar rats.

    PubMed

    Naraginti, Saraschandra; Kumari, P Lakshmi; Das, Raunak Kumar; Sivakumar, A; Patil, Sagar Hindurao; Andhalkar, Vaibhav Vilas

    2016-05-01

    Wound healing, a complex biological process, has attained a lot of attention as dermatologists are primarily interested in stimulated wound closure without formation of scar or a faint scar. The recent upsurgence of nanotechnology has provided novel therapeutic materials in the form of silver and gold nanoparticles which accelerate the wound healing process. The effect of formulated nanoparticles using Coleus forskohlii root extract (green synthesized) has been tried out for ameliorating full thickness excision wounds in albino Wistar male rats. The evaluation of in vivo activity of nanoparticles in wound healing was carried out on open wounds made by excision on the dorsal sides of albino Wistar rats under anesthesia, and the healing of the wounds was assessed. Histological aspects of the healing process were studied by a HE (Hematoxylin and Eosin) staining method to assess various degrees of re-epithelialization and the linear alignment of the granulation tissue whereas Van Gieson's histochemical staining was performed to observe collagen fibers. The healing action shown by the formulated nanoparticles was remarkable during the early stages of wound healing, which resulted in the substantial reduction of the whole healing period. Topical application of formulated gold nanoparticles was found to be more effective in suppressing inflammation and stimulating re-epithelialization compared to silver nanoparticles during the healing process. The results throw light on the amelioration of excision wounds using nanoparticles which could be a novel therapeutic way of improving wound healing in clinical practice. The mechanism of advanced healing action of both types of nanoparticles could be due to their antimicrobial, antioxidant and anti-inflammatory properties. PMID:26952426

  5. Excellent Electromagnetic Absorption Capability of Ni/Carbon Based Conductive and Magnetic Foams Synthesized via a Green One Pot Route.

    PubMed

    Zhao, Hai-Bo; Fu, Zhi-Bing; Chen, Hong-Bing; Zhong, Ming-Long; Wang, Chao-Yang

    2016-01-20

    Electromagnetic microwave absorption materials have attracted a great deal of attention. Foams for the low density and tunable porosity are considered as ideal microwave absorbents, while with the requirement of improving their inherent electromagnetic properties. In this manuscript, an innovative, easy, and green method was presented to synthesize an electromagnetic functionalized Ni/carbon foam, in which the formation of Ni nanoparticles and carbon occurred simultaneously from an affordable alginate/Ni(2+) foam precursor. The resultant Ni/carbon foam had a low density (0.1 g/cm(-3)) and high Ni nanoparticles loading (42 wt %). These Ni nanoparticles with a diameter of about 50-100 nm were highly crystallized and evenly embedded in porous graphite carbon without aggregation. Also, the resultant foam had a high surface area (451 m(2) g(-1)) and porosity and showed a moderate conductivity (6 S/m) and significant magnetism. Due to these special characteristics, the Ni/carbon foam exhibited greatly enhanced microwave absorption ability. Only with 10 wt % of functional fillers being used in the test template, the Ni/carbon foam based composite could reach an effective absorption bandwidth (below -10 dB) of 4.5 GHz and the minimum reflection value of -45 dB at 13.3 GHz with a thickness of 2 mm, while the traditional carbon foam and nano-Ni powder both showed very weak microwave absorption (the minimum reflection value < -10 dB). This foam was demonstrated to be a lightweight, high performance, and low filler loading microwave absorbing material. Furthermore, the detailed absorption mechanism of the foam was investigated. The result showed that the derived strong dielectric loss, including conductivity loss, interface polarization loss, weak magnetic loss, and naoporosity, contributes a great electromagnetic absorption. PMID:26710881

  6. Azadirachta indica plant-assisted green synthesis of Mn3O4 nanoparticles: Excellent thermal catalytic performance and chemical sensing behavior.

    PubMed

    Sharma, Jitendra Kumar; Srivastava, Pratibha; Ameen, Sadia; Akhtar, M Shaheer; Singh, Gurdip; Yadava, Sudha

    2016-06-15

    The leaf extract of Azadirachta indica (Neem) plant was utilized as reducing agent for the green synthesis of Mn3O4 nanoparticles (NPs). The crystalline analysis demonstrated the typical tetragonal hausmannite crystal structure of Mn3O4, which confirmed the formation of Mn3O4 NPs without the existence of other oxides. Green synthesized Mn3O4 NPs were applied for the catalytic thermal decomposition of ammonium perchlorate (AP) and as working electrode for fabricating the chemical sensor. The excellent catalytic effect for the thermal decomposition of AP was observed by decreasing the decomposition temperature by 175 °C with single decomposing step. The fabricated chemical sensor based on green synthesized Mn3O4 NPs displayed high, reliable and reproducible sensitivity of ∼569.2 μA mM(-1) cm(-2) with reasonable limit of detection (LOD) of ∼22.1 μM and the response time of ∼10 s toward the detection of 2-butanone chemical. A relatively good linearity in the ranging from ∼20 to 160 μM was detected for Mn3O4 NPs electrode based 2-butanone chemical sensor. PMID:27038784

  7. Chemical Vapor Deposition Synthesized Atomically Thin Molybdenum Disulfide with Optoelectronic-Grade Crystalline Quality.

    PubMed

    Bilgin, Ismail; Liu, Fangze; Vargas, Anthony; Winchester, Andrew; Man, Michael K L; Upmanyu, Moneesh; Dani, Keshav M; Gupta, Gautam; Talapatra, Saikat; Mohite, Aditya D; Kar, Swastik

    2015-09-22

    The ability to synthesize high-quality samples over large areas and at low cost is one of the biggest challenges during the developmental stage of any novel material. While chemical vapor deposition (CVD) methods provide a promising low-cost route for CMOS compatible, large-scale growth of materials, it often falls short of the high-quality demands in nanoelectronics and optoelectronics. We present large-scale CVD synthesis of single- and few-layered MoS2 using direct vapor-phase sulfurization of MoO2, which enables us to obtain extremely high-quality single-crystal monolayer MoS2 samples with field-effect mobility exceeding 30 cm(2)/(V s) in monolayers. These samples can be readily synthesized on a variety of substrates, and demonstrate a high-degree of optoelectronic uniformity in Raman and photoluminescence mapping over entire crystals with areas exceeding hundreds of square micrometers. Because of their high crystalline quality, Raman spectroscopy on these samples reveal a range of multiphonon processes through peaks with equal or better clarity compared to past reports on mechanically exfoliated samples. This enables us to investigate the layer thickness and substrate dependence of the extremely weak phonon processes at 285 and 487 cm(-1) in 2D-MoS2. The ultrahigh, optoelectronic-grade crystalline quality of these samples could be further established through photocurrent spectroscopy, which clearly reveal excitonic states at room temperature, a feat that has been previously demonstrated only on samples which were fabricated by micro-mechanical exfoliation and then artificially suspended across trenches. Our method reflects a big step in the development of atomically thin, 2D-MoS2 for scalable, high-quality optoelectronics. PMID:26256639

  8. Turn-off fluorescence sensor for the detection of ferric ion in water using green synthesized N-doped carbon dots and its bio-imaging.

    PubMed

    Edison, Thomas Nesakumar Jebakumar Immanuel; Atchudan, Raji; Shim, Jae-Jin; Kalimuthu, Senthilkumar; Ahn, Byeong-Cheol; Lee, Yong Rok

    2016-05-01

    This paper reports turn-off fluorescence sensor for Fe(3+) ion in water using fluorescent N-doped carbon dots as a probe. A simple and efficient hydrothermal carbonization of Prunus avium fruit extract for the synthesis of fluorescent nitrogen-doped carbon dots (N-CDs) is described. This green approach proceeds quickly and provides good quality N-CDs. The mean size of synthesized N-CDs was approximately 7nm calculated from the high-resolution transmission electron microscopic images. X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy revealed the presence of -OH, -NH2, -COOH, and -CO functional groups over the surface of CDs. The N-CDs showed excellent fluorescent properties, and emitted blue fluorescence at 411nm upon excitation at 310nm. The calculated quantum yield of the synthesized N-CDs is 13% against quinine sulfate as a reference fluorophore. The synthesized N-CDs were used as a fluorescent probe towards the selective and sensitive detection of biologically important Fe(3+) ions in water by fluorescence spectroscopy and for bio-imaging of MDA-MB-231 cells. The limit of detection (LOD) and the Stern-Volmer quenching constant for the synthesized N-CDs were 0.96μM and 2.0958×10(3)M of Fe(3+) ions. The green synthesized N-CDs are efficiently used as a promising candidate for the detection of Fe(3+) ions and bio-imaging. PMID:26994332

  9. DEVELOPMENT OF ENVIRONMENTAL INDICES FOR GREEN CHEMICAL PRODUCTION AND USE

    EPA Science Inventory

    Chemical production, use and disposal cause adverse impacts on the environment. Consequently, much research has been conducted to develop methods for estimating the risk of chemicals and to screen them based on environmental impact. Risk assessment may be subdivide...

  10. Microstructural, chemical and textural characterization of ZnO nanorods synthesized by aerosol assisted chemical vapor deposition

    SciTech Connect

    Sáenz-Trevizo, A.; Amézaga-Madrid, P.; Fuentes-Cobas, L.; Pizá-Ruiz, P.; Antúnez-Flores, W.; Ornelas-Gutiérrez, C.; Pérez-García, S.A.; Miki-Yoshida, M.

    2014-12-15

    ZnO nanorods were synthesized by aerosol assisted chemical vapor deposition onto TiO{sub 2} covered borosilicate glass substrates. Deposition parameters were optimized and kept constant. Solely the effect of different nozzle velocities on the growth of ZnO nanorods was evaluated in order to develop a dense and uniform structure. The crystalline structure was characterized by conventional X-ray diffraction in grazing incidence and Bragg–Brentano configurations. In addition, two-dimensional grazing incidence synchrotron radiation diffraction was employed to determine the preferred growth direction of the nanorods. Morphology and growth characteristics analyzed by electron microscopy were correlated with diffraction outcomes. Chemical composition was established by X-ray photoelectron spectroscopy. X-ray diffraction results and X-ray photoelectron spectroscopy showed the presence of wurtzite ZnO and anatase TiO{sub 2} phases. Morphological changes noticed when the deposition velocity was lowered to the minimum, indicated the formation of relatively vertically oriented nanorods evenly distributed onto the TiO{sub 2} buffer film. By coupling two-dimensional X-ray diffraction and computational modeling with ANAELU it was proved that a successful texture determination was achieved and confirmed by scanning electron microscopy analysis. Texture analysis led to the conclusion of a preferred growth direction in [001] having a distribution width Ω = 20° ± 2°. - Highlights: • Uniform and pure single-crystal ZnO nanorods were obtained by AACVD technique. • Longitudinal and transversal axis parallel to the [001] and [110] directions, respectively. • Texture was determined by 2D synchrotron diffraction and electron microscopy analysis. • Nanorods have its [001] direction distributed close to the normal of the substrate. • Angular spread about the preferred orientation is 20° ± 2°.

  11. Physico-Chemical Structural and Electrical Studies of Cu-Zn Ferrites Synthesized by Novel Chemical Route

    NASA Astrophysics Data System (ADS)

    Lohar, K. S.; Patange, S. M.; Mane, D. R.; Shirsath, Sagar E.; Shinde, N. D.; Kulkarni, Nilesh

    The physico-chemical, structural and electrical properties of zinc substituted copper ferrites having the general formula Cu1-xZnxFe2O4 (x=0.0 to x=0.8) have been studied as a function of zinc ion concentration. The sample was prepared by co-precipitation method from corresponding metal sulphates. X-ray diffraction patterns were used to confirm the structure of synthesized samples. The calculated and theoretical values of average lattice constant, tetrahedral bond, tetrahedral edge and unshared octahedral edge were found to increase, while the shared octahedral edge and octahedral bond decrease as the Zn ion concentration increases. The dielectric constant (ε‧) and dielectric loss tangent (tan δ) were measured at a constant frequency 1 kHz as a function of temperature. The dielectric constant and loss tangent were found to increase with rise in temperature. The conduction mechanism in these ferrites is discussed on the basis of electron exchange between Fe2+ and Fe3+ ions. The temperature dependent dc resistivity was carried out in the temperature range 300 to 800 K. The plots of log ρ versus 103/T are linear showing two regions, corresponding to ferrimagnetic and paramagnetic regions.

  12. Diameter control of single wall carbon nanotubes synthesized using chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Roy, Soumyendu; Bajpai, Reeti; Soin, Navneet; Roy, Susanta Sinha; McLaughlin, James A.; Misra, D. S.

    2014-12-01

    Lack of control on the chirality or diameter of single-wall carbon nanotubes (SWCNTs) during synthesis is a major impediment in the path of their widespread commercialization. We demonstrate that the humble technique of catalytic chemical vapor deposition of methane, without any sophisticated catalyst preparation, can provide significant control on the diameter of the synthesized SWCNTs. The catalyst used is a solid solution of the bimetals Fe-Mo or Co-Mo in MgO. The radial breathing modes (RBMs) in the Raman spectra of SWCNTs were used to find out the diameters. Kataura plot along with RBMs was used to study the chirality of the tubes. High concentration of the catalysts (Co:Mo:MgO = 1:0.5:15 and Fe:Mo:MgO = 1:0.5:30) resulted in high yields. However, most of these carbonaceous materials were impurities. Reducing the concentration not only improved the purity and crystallinity (ID/IG ratio ∼0.1), but most importantly reduced the diameter spread of the SWCNTs. Majority of the SWCNTs grown using the low concentration catalysts (Co:Mo:MgO = 1:0.5:300 and Fe:Mo:MgO = 1:0.5:200) were estimated to have diameters lying between 1.13 and 1.65 nm. This narrowing of diameter spread happened for both Fe and Co catalyst systems and depended only on the concentration of the catalyst.

  13. Industrial-scale proteomics: from liters of plasma to chemically synthesized proteins.

    PubMed

    Rose, Keith; Bougueleret, Lydie; Baussant, Thierry; Böhm, Günter; Botti, Paolo; Colinge, Jacques; Cusin, Isabelle; Gaertner, Hubert; Gleizes, Anne; Heller, Manfred; Jimenez, Silvia; Johnson, Andrew; Kussmann, Martin; Menin, Laure; Menzel, Christoph; Ranno, Frederic; Rodriguez-Tomé, Patricia; Rogers, John; Saudrais, Cedric; Villain, Matteo; Wetmore, Diana; Bairoch, Amos; Hochstrasser, Denis

    2004-07-01

    Human blood plasma is a useful source of proteins associated with both health and disease. Analysis of human blood plasma is a challenge due to the large number of peptides and proteins present and the very wide range of concentrations. In order to identify as many proteins as possible for subsequent comparative studies, we developed an industrial-scale (2.5 liter) approach involving sample pooling for the analysis of smaller proteins (M(r) generally < ca. 40 000 and some fragments of very large proteins). Plasma from healthy males was depleted of abundant proteins (albumin and IgG), then smaller proteins and polypeptides were separated into 12 960 fractions by chromatographic techniques. Analysis of proteins and polypeptides was performed by mass spectrometry prior to and after enzymatic digestion. Thousands of peptide identifications were made, permitting the identification of 502 different proteins and polypeptides from a single pool, 405 of which are listed here. The numbers refer to chromatographically separable polypeptide entities present prior to digestion. Combining results from studies with other plasma pools we have identified over 700 different proteins and polypeptides in plasma. Relatively low abundance proteins such as leptin and ghrelin and peptides such as bradykinin, all invisible to two-dimensional gel technology, were clearly identified. Proteins of interest were synthesized by chemical methods for bioassays. We believe that this is the first time that the small proteins in human blood plasma have been separated and analyzed so extensively. PMID:15221774

  14. Study on antibacterial activity of chemically synthesized PANI-Ag-Au nanocomposite

    NASA Astrophysics Data System (ADS)

    Boomi, Pandi; Prabu, Halliah Gurumallesh; Manisankar, Paramasivam; Ravikumar, Sundaram

    2014-05-01

    Pristine polyaniline (PANI), PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites have been successfully synthesized by chemical oxidative polymerization method using aniline as monomer, ammonium persulphate as oxidant and metal (Ag, Au and Ag-Au) colloids. UV-Vis analysis exhibited surface Plasmon resonances of Ag, Au, Ag-Au nanoparticles. FT-IR spectra revealed the shift in peak position of N-H stretching. X-ray diffraction (XRD) results confirm the presence of Ag, Au and Au-Ag nanoparticles. HR-TEM images show nanosizes of Ag, Au, Ag-Au and the incorporation of such nanoparticles into the PANI matrix. Pristine PANI, PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites were tested for antibacterial activity by agar well diffusion method. PANI-Ag-Au nanocomposite exhibited higher antibacterial activity against both gram-positive [Streptococcus sp. (MTCC 890), Staphylococcus sp. (MTCC 96)] and gram-negative bacteria [Escherichia coli (MTCC 1671) and Klebsiella sp. (MTCC 7407)] when compared with PANI-Ag nanocomposite, PANI-Au nanocomposite and pristine PANI. The novelty of this study is the polymer-bimetal synthesis and its antibacterial potential.

  15. Chemical egg defense in a green lacewing (Ceraeochrysa smithi)

    PubMed Central

    Eisner, T; Attygalle, A B; Conner, W E; Eisner, M; MacLeod, E; Meinwald, J

    1996-01-01

    The green lacewing Ceraeochrysa smithi (Neuroptera, Chrysopidae), like other members of its family, lays its eggs on stalks, but it is unusual in that it coats these stalks with droplets of an oily fluid. The liquid consists of a mixture of fatty acids, an ester, and a series of straight-chain aldehydes. Relative to the eggs of a congeneric chrysopid that lacks stalk fluid, the eggs of C. smithi proved well protected against ants. Components of the fluid, in an assay with a cockroach, proved potently irritant. Following emergence from the egg, C. smithi larvae imbibe the stalk fluid, thereby possibly deriving nutritive benefit, defensive advantage, or both. Images Fig. 1 PMID:8622928

  16. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach.

    PubMed

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-11

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a 'dip-in and light-irradiation' green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems. PMID:24622377

  17. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach

    NASA Astrophysics Data System (ADS)

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-01

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a ‘dip-in and light-irradiation’ green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems.

  18. Green Jobs: Definition and Method of Appraisal of Chemical and Biological Risks.

    PubMed

    Cheneval, Erwan; Busque, Marc-Antoine; Ostiguy, Claude; Lavoie, Jacques; Bourbonnais, Robert; Labrèche, France; Bakhiyi, Bouchra; Zayed, Joseph

    2016-04-01

    In the wake of sustainable development, green jobs are developing rapidly, changing the work environment. However a green job is not automatically a safe job. The aim of the study was to define green jobs, and to establish a preliminary risk assessment of chemical substances and biological agents for workers in Quebec. An operational definition was developed, along with criteria and sustainable development principles to discriminate green jobs from regular jobs. The potential toxicity or hazard associated with their chemical and biological exposures was assessed, and the workers' exposure appraised using an expert assessment method. A control banding approach was then used to assess risks for workers in selected green jobs. A double entry model allowed us to set priorities in terms of chemical or biological risk. Among jobs that present the highest risk potential, several are related to waste management. The developed method is flexible and could be adapted to better appraise the risks that workers are facing or to propose control measures. PMID:26718400

  19. Angiostatic effects of Brazilian green propolis and its chemical constituents.

    PubMed

    Chikaraishi, Yuichi; Izuta, Hiroshi; Shimazawa, Masamitsu; Mishima, Satoshi; Hara, Hideaki

    2010-04-01

    Propolis, a resinous substance collected by honeybees from various plant sources, has several pharmacological actions, such as anti-tumor and anti-inflammatory effects. The aim of this study was to evaluate the anti-angiogenic effects of a water extract of Brazilian green propolis (WEP) and its constituents, caffeoylquinic acid derivatives, against angiogenic processes in human umbilical vein endothelial cells (HUVECs) in vitro. We also examined the anti-angiogenic effects of WEP against retinal neovascularization in a murine oxygen-induced retinopathy model in vivo. WEP and its constituents significantly suppressed vascular endothelial growth factor (VEGF)-induced HUVEC proliferation, migration, and tube formation in vitro. WEP and its caffeoylquinic acid derivatives suppressed VEGF-stimulated phosphorylation of mitogen-activated protein kinase in HUVECs (versus VEGF alone). Moreover, WEP (300 mg/kg/day, subcutaneously for 5 days) significantly suppressed retinal neovascularization in the murine oxygen-induced retinopathy model. These data indicate that (i) WEP has angiostatic effects against angiogenic processes in vitro and in an in vivo model of murine oxygen-induced retinopathy and (ii) the inhibitory effects of WEP against in vitro angiogenesis are chiefly derived from its caffeoylquinic acid derivatives. Judging from these findings, WEP and its caffeoylquinic acid derivatives may represent candidates for preventive or therapeutic agents against diseases caused by angiogenesis. PMID:19960454

  20. Chemical cleaning re-invented: clean, lean and green.

    PubMed

    Hanson, Margaret; Vangeel, Michel

    2014-01-01

    A project undertaken in the Central Cleaning Department of Janssen, a Johnson and Johnson pharmaceutical company, demonstrates how ergonomics, environmental and industrial hygiene risks and quality concerns can be tackled simultaneously. The way equipment was cleaned was re-designed by an in-house cross-functional team to ensure a 'clean, lean and green' process. Initiatives included a new layout of the area, and new work processes and equipment to facilitate cleaning and handling items. This resulted in significant improvements: all ergonomics high risk tasks were reduced to moderate or low risk; hearing protection was no longer required; respirator requirement reduced by 67%; solvent use reduced by 73%; productivity improved, with 55% fewer operator hours required; and quality improved 40-fold. The return on investment was estimated at 3.125 years based on an investment of over €1.5 million (2008 prices). This win-win intervention allowed ergonomics, environmental, industrial hygiene, productivity and quality concerns all to be addressed. PMID:24858515

  1. Green process for chemical functionalization of nanocellulose with carboxylic acids.

    PubMed

    Espino-Pérez, Etzael; Domenek, Sandra; Belgacem, Naceur; Sillard, Cécile; Bras, Julien

    2014-12-01

    An environmentally friendly and simple method, named SolReact, has been developed for a solvent-free esterification of cellulose nanocrystals (CNC) surface by using two nontoxic carboxylic acids (CA), phenylacetic acid and hydrocinnamic acid. In this process, the carboxylic acids do not only act as grafting agent, but also as solvent media above their melting point. Key is the in situ solvent exchange by water evaporation driving the esterification reaction without drying the CNC. Atomic force microscopy and X-ray diffraction analyses showed no significant change in the CNC dimensions and crystallinity index after this green process. The presence of the grafted carboxylic was characterized by analysis of the "bulk" CNC with elemental analysis, infrared spectroscopy, and (13)C NMR. The ability to tune the surface properties of grafted nanocrystals (CNC-g-CA) was evaluated by X-ray photoelectron spectroscopy analysis. The hydrophobicity behavior of the functionalized CNC was studied through the water contact-angle measurements and vapor adsorption. The functionalization of these bionanoparticles may offer applications in composite manufacturing, where these nanoparticles have limited dispersibility in hydrophobic polymer matrices and as nanoadsorbers due to the presence of phenolic groups attached on the surface. PMID:25353612

  2. Effects of natural and chemically synthesized furanones on quorum sensing in Chromobacterium violaceum

    PubMed Central

    Martinelli, Daniel; Grossmann, Gilles; Séquin, Urs; Brandl, Helmut; Bachofen, Reinhard

    2004-01-01

    Background Cell to cell signaling systems in Gram-negative bacteria rely on small diffusible molecules such as the N-acylhomoserine lactones (AHL). These compounds are involved in the production of antibiotics, exoenzymes, virulence factors and biofilm formation. They belong to the class of furanone derivatives which are frequently found in nature as pheromones, flavor compounds or secondary metabolites. To obtain more information on the relation between molecular structure and quorum sensing, we tested a variety of natural and chemically synthesized furanones for their ability to interfere with the quorum sensing mechanism using a quantitative bioassay with Chromobacterium violaceum CV026 for antagonistic and agonistic action. We were looking at the following questions: 1. Do these compounds affect growth? 2) Do these compounds activate the quorum sensing system of C. violaceum CV026? 3) Do these compounds inhibit violacein formation induced by the addition of the natural inducer N-hexanoylhomoserine lactone (HHL)? 4) Do these compounds enhance violacein formation in presence of HHL? Results The naturally produced N-acylhomoserine lactones showed a strong non-linear concentration dependent influence on violacein production in C. violaceum with a maximum at 3.7*10-8 M with HHL. Apart from the N-acylhomoserine lactones only one furanone (emoxyfurane) was found to simulate N-acylhomoserine lactone activity and induce violacein formation. The most effective substances acting negatively both on growth and quorum sensing were analogs and intermediates in synthesis of the butenolides from Streptomyces antibioticus. Conclusion As the regulation of many bacterial processes is governed by quorum sensing systems, the finding of natural and synthetic furanones acting as agonists or antagonists suggests an interesting tool to control and handle detrimental AHL induced effects. Some effects are due to general toxicity; others are explained by a competitive interaction for Lux

  3. The science of green chemistry and its role in chemicals policy and educational reform.

    PubMed

    Cannon, Amy S; Warner, John C

    2011-01-01

    Over the past 10 years, the science of green chemistry has continued to evolve and has been adopted in research labs in industry and academia. At the same time, new innovations in chemicals policy have widened opportunities for legislative action to protect human health and the environment. This article addresses the mechanisms by which the science of green chemistry and chemicals policy can work together to help attain a more sustainable future. It also speaks to the pitfalls of inappropriately merging these two, and explores how such a merger could inhibit the creation of sustainable technologies. Green chemistry's role in educational reform is discussed as a means for training students who are prepared to create truly sustainable technologies. PMID:22001044

  4. Green chemical synthesis of silver nanomaterials with maltodextrin.

    SciTech Connect

    Tallant, David Robert; Lu, Ping; Lambert, Timothy N.; Bell, Nelson Simmons

    2010-11-01

    Silver nanomaterials have significant application resulting from their optical properties related to surface enhanced Raman spectroscopy, high electrical conductivity, and anti-microbial impact. A 'green chemistry' synthetic approach for silver nanomaterials minimizes the environmental impact of silver synthesis, as well as lowers the toxicity of the reactive agents. Biopolymers have long been used for stabilization of silver nanomaterials during synthesis, and include gum Arabic, heparin, and common starch. Maltodextrin is a processed derivative of starch with lower molecular weight and an increase in the number of reactive reducing aldehyde groups, and serves as a suitable single reactant for the formation of metallic silver. Silver nanomaterials can be formed under either a thermal route at neutral pH in water or by reaction at room temperature under more alkaline conditions. Deposited silver materials are formed on substrates from near neutral pH solutions at low temperatures near 50 C. Experimental conditions based on material concentrations, pH and reaction time are investigated for development of deposited films. Deposit morphology and optical properties are characterized using SEM and UV-vis techniques. Silver nanoparticles are generated under alkaline conditions by a dissolution-reduction method from precipitated silver (II) oxide. Synthesis conditions were explored for the rapid development of stable silver nanoparticle dispersions. UV-vis absorption spectra, powder X-ray diffraction (PXRD), dynamic light scattering (DLS), and transmission electron microscopy (TEM) techniques were used to characterize the nanoparticle formation kinetics and the influence of reaction conditions. The adsorbed content of the maltodextrin was characterized using thermogravimetric analysis (TGA).

  5. Effect of annealing on the structure of chemically synthesized SnO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Singh, Kulwinder; Kumar, Virender; Vij, Ankush; Kumari, Sudesh; Kumar, Akshay; Thakur, Anup

    2016-05-01

    Tin oxide (SnO2) nanoparticles have been synthesized by co-precipitation method. The synthesized nanoparticles were characterized by X-ray diffraction (XRD) and Raman spectroscopy. XRD analysis confirmed the single phase formation of SnO2 nanoparticles. The Raman shifts showed the typical feature of the tetragonal phase of the as-synthesized SnO2 nanoparticles. At low annealing temperature, a strong distortion of the crystalline structure and high degree of agglomeration was observed. It is concluded that the crystallinity of SnO2 nanoparticles improves with the increase in annealing temperature.

  6. Mosquito larvicidal and antimicrobial activity of synthesized nano-crystalline silver particles using leaves and green berry extract of Solanum nigrum L. (Solanaceae: Solanales).

    PubMed

    Rawani, Anjali; Ghosh, Anupam; Chandra, Goutam

    2013-12-01

    Silver nanoparticles (AgNPs) that are synthesized by using aqueous extracts of Solanum nigrum L., is a simple, non-toxic and ecofriendly green material. The present study is based on assessments of the larvicidal and antimicrobial activities of the synthesized AgNPs from fresh leaves, dry leaves and green berries of S. nigrum against larvae of Culex quinquefasciatus and Anopheles stephensi and four human pathogenic and five fish pathogenic bacteria respectively. The synthesized nanoparticles are characterized with UV-vis spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscope (TEM) analysis. The nanoparticles are spherical to polyhedral in shape with size of 50-100nm (average size of 56.6nm). In larvicidal bioassay with synthesized AgNPs, highest mortality are observed at 10ppm against An. stephensi with LC50 values of 1.33, 1.59, 1.56ppm and LC90 values of 3.97, 7.31, 4.76ppm for dry leaves, fresh leaves and berries respectively. Antibacterial activity test reveals better results against fish pathogenic bacteria than human pathogenic bacteria. Non target organism like Toxorhynchites larvae (mosquito predator), Diplonychus annulatum (predatory water-bug) and Chironomus circumdatus larvae (chironomid) are also exposed to respective lethal concentrations (to mosquito larvae) of dry nanoparticles and no abnormality in the non target organisms are recorded. These results suggest that the synthesized AgNPs of S. nigrum have the potential to be used as an ideal eco-friendly compound for the control of the mosquito larvae and harmful bacteria. PMID:24055718

  7. Mosquitocidal and antibacterial activity of green-synthesized silver nanoparticles from Aloe vera extracts: towards an effective tool against the malaria vector Anopheles stephensi?

    PubMed

    Dinesh, Devakumar; Murugan, Kadarkarai; Madhiyazhagan, Pari; Panneerselvam, Chellasamy; Kumar, Palanisamy Mahesh; Nicoletti, Marcello; Jiang, Wei; Benelli, Giovanni; Chandramohan, Balamurugan; Suresh, Udaiyan

    2015-04-01

    Mosquitoes represent an important threat for lives of millions of people worldwide, acting as vectors for devastating pathogens, such as malaria, yellow fever, dengue, and West Nile. In addition, pathogens and parasites polluting water also constitute a severe plague for populations of developing countries. Here, we investigated the mosquitocidal and antibacterial properties of Aloe vera leaf extract and silver nanoparticles synthesized using A. vera extract. Mosquitocidal properties were assessed in laboratory against larvae (I-IV instar) and pupae of the malaria vector Anopheles stephensi. Green-synthesized silver nanoparticles were tested against An. stephensi also in field conditions. Antibacterial properties of nanoparticles were evaluated against Bacillus subtilis, Klebsiella pneumoniae, and Salmonella typhi using the agar disk diffusion and minimum inhibitory concentration protocol. The synthesized silver nanoparticles were characterized by UV-vis spectrum, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). In laboratory conditions, the A. vera extract was toxic against An. stephensi larvae and pupae, even at low dosages. LC50 were 48.79 ppm (I instar), 59.09 ppm (II instar), 70.88 ppm (III instar), 83.58 ppm (IV instar), and 152.55 ppm (pupae). Green-synthesized silver nanoparticles were highly toxic against An. stephensi. LC50 were 3.825 ppm (I instar), 4.119 ppm (II instar), 4.982 ppm (III instar), 5.711 ppm (IV instar), and 6.113 ppm (pupae). In field conditions, the application of A. vera-synthesized silver nanoparticles (10 × LC50) leads to An. stephensi larval reduction of 74.5, 86.6, and 97.7%, after 24, 48, and 72 h, respectively. Nanoparticles also showed antibacterial properties, and the maximum concentration tested (150 mg/L) evoked an inhibition zone wider than 80 mm in all tested bacterium species. This study adds knowledge about the use of green synthesis of nanoparticles in

  8. Solution-Processed Carbon Nanotube and Chemically Synthesized Graphene Nanoribbon Field Effect Transistors

    NASA Astrophysics Data System (ADS)

    Bennett, Patrick Bryce

    in order to study the performance of solution-processed CNT devices. TFT performance is limited by metallic CNTs that can short channels, but can be improved by structuring the CNT film, either through patterning or induced alignment. Increasing semiconducting CNT purity does not necessarily increase device performance because of the decreased lengths of the purified CNTs. Extremely high purity semiconducting CNT solutions, however, are not subject to these same limitations, with transistors exhibiting improved mobilities while also scaling to sub-microm channel lengths. Short channel devices down to 15 nm are then presented, demonstrating ballistic transport in solution-processed CNTs, despite their inferior electronic performance at microm-scale lengths. Finally, short channel devices utilizing chemically synthesized GNRs as channels are presented and characterized to directly probe the mechanisms of electron transport in these materials for the first time.

  9. Active biopolymers in green non-conventional media: a sustainable tool for developing clean chemical processes.

    PubMed

    Lozano, Pedro; Bernal, Juana M; Nieto, Susana; Gomez, Celia; Garcia-Verdugo, Eduardo; Luis, Santiago V

    2015-12-21

    The greenness of chemical processes turns around two main axes: the selectivity of catalytic transformations, and the separation of pure products. The transfer of the exquisite catalytic efficiency shown by enzymes in nature to chemical processes is an important challenge. By using appropriate reaction systems, the combination of biopolymers with supercritical carbon dioxide (scCO2) and ionic liquids (ILs) resulted in synergetic and outstanding platforms for developing (multi)catalytic green chemical processes, even under flow conditions. The stabilization of biocatalysts, together with the design of straightforward approaches for separation of pure products including the full recovery and reuse of enzymes/ILs systems, are essential elements for developing clean chemical processes. By understanding structure-function relationships of biopolymers in ILs, as well as for ILs themselves (e.g. sponge-like ionic liquids, SLILs; supported ionic liquids-like phases, SILLPs, etc.), several integral green chemical processes of (bio)catalytic transformation and pure product separation are pointed out (e.g. the biocatalytic production of biodiesel in SLILs, etc.). Other developments based on DNA/ILs systems, as pathfinder studies for further technological applications in the near future, are also considered. PMID:26497761

  10. Quantum chemical modelling of ``green'' luminescence in ABO perovskites

    NASA Astrophysics Data System (ADS)

    Eglitis, R. I.; Kotomin, E. A.; Borstel, G.

    2002-06-01

    The origin of the intrinsic excitonic (``green'') luminescence in ABO3 perovskites remains a hot topic over the last quarter of a century. We suggest as a theoretical interpretation for the ``green'' luminescence in these crystals, the recombination of electron and hole polarons forming a charge transfer vibronic exciton. In order to check quantitatively the proposed model, we performed quantum chemical calculations using the Intermediate Neglect of Differential Overlap (INDO) method combined with the periodic defect model. The luminescence energies calculated for four perovskite crystals are found to be in good agreement with experimental data.

  11. Inhibition of pathogenic bacterial growth on excision wound by green synthesized copper oxide nanoparticles leads to accelerated wound healing activity in Wistar Albino rats.

    PubMed

    Sankar, Renu; Baskaran, Athmanathan; Shivashangari, Kanchi Subramanian; Ravikumar, Vilwanathan

    2015-07-01

    An impaired wound healing is one of the major health related problem in diabetic and non-diabetic patients around the globe. The pathogenic bacteria play a predominant role in delayed wound healing, owing to interaction in the wound area. In our previous work we developed green chemistry mediated copper oxide nanoparticles using Ficus religiosa leaf extract. In the present study we make an attempt to evaluate the anti-bacterial, and wound healing activity of green synthesized copper oxide nanoparticles in male Wistar Albino rats. The agar well diffusion assay revealed copper oxide nanoparticles have substantial inhibition activity against human pathogenic strains such as Klebsiella pneumoniae, Shigella dysenteriae, Staphylococcus aureus, Salmonella typhimurium and Escherichia coli, which were responsible for delayed wound healing process. Furthermore, the analyses results of wound closure, histopathology and protein profiling confirmed that the F. religiosa leaf extract tailored copper oxide nanoparticles have enhanced wound healing activity in Wistar Albino rats. PMID:26194977

  12. Chemical synthesis of the precursor molecule of the Aequorea green fluorescent protein, subsequent folding, and development of fluorescence

    PubMed Central

    Nishiuchi, Yuji; Inui, Tatsuya; Nishio, Hideki; Bódi, József; Kimura, Terutoshi; Tsuji, Frederick I.; Sakakibara, Shumpei

    1998-01-01

    The present paper describes the total chemical synthesis of the precursor molecule of the Aequorea green fluorescent protein (GFP). The molecule is made up of 238 amino acid residues in a single polypeptide chain and is nonfluorescent. To carry out the synthesis, a procedure, first described in 1981 for the synthesis of complex peptides, was used. The procedure is based on performing segment condensation reactions in solution while providing maximum protection to the segment. The effectiveness of the procedure has been demonstrated by the synthesis of various biologically active peptides and small proteins, such as human angiogenin, a 123-residue protein analogue of ribonuclease A, human midkine, a 121-residue protein, and pleiotrophin, a 136-residue protein analogue of midkine. The GFP precursor molecule was synthesized from 26 fully protected segments in solution, and the final 238-residue peptide was treated with anhydrous hydrogen fluoride to obtain the precursor molecule of GFP containing two Cys(acetamidomethyl) residues. After removal of the acetamidomethyl groups, the product was dissolved in 0.1 M Tris⋅HCl buffer (pH 8.0) in the presence of DTT. After several hours at room temperature, the solution began to emit a green fluorescence (λmax = 509 nm) under near-UV light. Both fluorescence excitation and fluorescence emission spectra were measured and were found to have the same shape and maxima as those reported for native GFP. The present results demonstrate the utility of the segment condensation procedure in synthesizing large protein molecules such as GFP. The result also provides evidence that the formation of the chromophore in GFP is not dependent on any external cofactor. PMID:9811837

  13. Ultrastructural and Chemical Evidence That the Cell Wall of Green Cotton Fiber Is Suberized 1

    PubMed Central

    Yatsu, L. Y.; Espelie, Karl E.; Kolattukudy, P. E.

    1983-01-01

    Green cotton (Gossypium hirsutum L.) fibers were shown by electron microscopy to have numerous thin concentric rings around the lumen of the cell. These rings possessed a lamellar fine structure characteristic of suberin. LiA1D4 depolymerization and gas chromatography-mass spectrometry analysis showed the presence of a suberin polymer in the green cotton with the major aliphatic monomers being ω-hydroxydocosanoic acid (70%) and docosanedoic acid (25%). Ordinary white cotton was shown by chemical and ultrastructural examination to be encircled by a thin cuticular polymer containing less than 0.5% of the aliphatic components found in green cotton. Images Fig. 1 Fig. 2 Fig. 3 Fig. 4 PMID:16663251

  14. A top-down strategy to synthesize wurtzite Cu2ZnSnS4 nanocrystals by green chemistry.

    PubMed

    Sun, Yiwen; Hu, Zhengqiao; Zhang, Junjun; Wang, Li; Wu, Chunyan; Xu, Jun

    2016-07-28

    Green synthesis of metastable wurtzite Cu2ZnSnS4 nanocrystals through a top-down synthetic strategy is presented. Formation mechanisms associated with Kirkendall and etching effects are illustrated in detail. The nanocrystals exhibit remarkable photoluminescence properties at room temperature. PMID:27427432

  15. Physical, chemical and nutritional characteristics of premature-processed and matured green legumes.

    PubMed

    Bhattacharya, Sila; Malleshi, N G

    2012-08-01

    Premature green legumes are good sources of nutraceuticals and antioxidants and are consumed as snacks as well as vegetables. They are seasonal and have limited shelf-life. Efforts are provided to prepare shelf-stable green legumes to extend their availability throughout the year. Green legumes from chick pea or Bengal gram (Cicer arietinum) and field bean (Dolichos lablab) have been processed to enhance their shelf-life, and determined their nutritional, physico-chemical and nutraceutical qualities. The shelf stable green legumes (SSGL) show higher water absorption capacity compared to matured dry legumes (MDL). The total colour change in the processed/dried SSGL and MDL samples increased significantly (p ≤ 0.05) compared to the freshly harvested green samples. The carotenoid content of Bengal gram and field bean SSGLs are 8.0 and 3.2 mg/100 g, and chlorophyll contents are 12.5 and 0.5 mg/100 g, respectively, which are in negligible quantities in matured legumes; the corresponding polyphenol contents are 197.8 and 153.1 mg/100 g. These results indicate that SSGLs possess potential antioxidant activity. PMID:23904654

  16. [Comparison of green coffee beans volatiles chemical composition of Hainan main area].

    PubMed

    Hu, Rong-Suo; Chu, Zhong; Gu, Feng-Lin; Lu, Min-Quan; Lu, Shao-Fang; Wu, Gui-Ping; Tan, Le-He

    2013-02-01

    Chemical component of Hainan green coffee beans was analyzed with solid phase microextraction-gas chromatography-mass spectrometry, and the discrepancy between two green coffee beans was differentiated through the spectrum database retrieval and retention index of compound characterization. The experimental results show that: the chemical composition of Wanning coffee beans and Chengmai coffee beans is basically the same. The quantity of analyzed compound in Wanning area coffee is 91, and in Chengmai area coffee is 106, the quantity of the same compound is 66, and the percent of the same component is 75.52%. The same compounds accounted for 89.86% of the total content of Wanning area coffee, and accounted for 85.70% of the total content of Chengmai area coffee. PMID:23697152

  17. Influence of Sn on the magnetic ordering of Ni-Sn alloy synthesized using chemical reduction method

    NASA Astrophysics Data System (ADS)

    Dhanapal, K.; Narayanan, V.; Stephen, A.

    2016-05-01

    The Ni-Sn alloy was synthesized using borohydride assisted chemical reduction method. The composition of the synthesized alloy was determined using atomic absorption spectroscopy which revealed that the observed composition of Sn is high when compared to the initial composition. The ultrafine particles are clearly observed from field emission scanning electron microscope for all the sample. The X-ray diffraction measurement confirmed that the as-synthesized samples are of amorphous like nature while the samples annealed at 773 K showed crystalline nature. The Fourier transform infrared spectroscopy confirmed metallic bond stretching in the alloy samples. The crystallization and phase transition temperature was observed from differential scanning calorimetry. The shift in the crystallization temperature of Ni with increasing percentage of Sn was observed. The vibrating sample magnetometer was employed to understand the magnetic behavior of the Ni-Sn alloy. As-synthesized alloy samples showed paramagnetic nature while the annealed ones exhibit the soft ferromagnetic, antiferromagnetic and paramagnetic nature. The saturation magnetization value and magnetic ordering in the Ni-Sn alloys depend on the percentage of Sn present in the alloy.

  18. Greener Syntheses and Chemical Transformations: Sustainable Alternative Methods and Applications of Nano-Catalysts. (Florence, Italy)

    EPA Science Inventory

    The presentation summarizes our sustainable chemical synthesis activity involving benign alternatives, such as the use of supported reagents, and greener reaction medium in aqueous or solvent-free conditions. The synthesis of heterocyclic compounds, coupling reactions, and a vari...

  19. Greener Syntheses and Chemical Transformations: Sustainable Alternative Methods and Applications of Nano-Catalysts

    EPA Science Inventory

    The presentation summarizes our sustainable chemical synthesis activity involving benign alternatives, such as the use of supported reagents, and greener reaction medium in aqueous or solvent-free conditions.1 The synthesis of heterocyclic compounds, coupling reactions, and a var...

  20. Greener Syntheses and Chemical Transformations Using SustainableAlternative Methods and Nano-Catalysts

    EPA Science Inventory

    The presentation summarizes our sustainable chemical synthesis activity involving benign alternatives, namely greener reaction medium in aqueous or solventfree conditions and using alternative activation via microwave or photocatalytic activation. Eco-friendly synthesis of nanoma...

  1. A one-step green route to synthesize copper nanocrystals and their applications in catalysis and surface enhanced Raman scattering

    NASA Astrophysics Data System (ADS)

    Zhang, Pinhua; Sui, Yongming; Wang, Chao; Wang, Yingnan; Cui, Guangliang; Wang, Chunzhong; Liu, Bingbing; Zou, Bo

    2014-04-01

    A nontoxic, simple, inexpensive, and reproducible strategy, which meets the standard of green chemistry, is introduced for the synthesis of copper nanocrystals (Cu NCs) with olive oil as both reducing agent and capping agent. By changing the reaction parameters, the shape, size and surface structure of the Cu NCs can be well controlled. The obtained Cu nanocubes show excellent catalytic properties for the catalytic reduction of dyes and CO oxidation. Moreover, the prepared Cu nanocubes as substrates exhibit surface enhanced Raman scattering (SERS) activity for 4-mercaptopyridine (4-Mpy). Therefore, this facile route provides a useful platform for the fabrication of Cu NCs which have the potential to replace noble metals for certain applications.A nontoxic, simple, inexpensive, and reproducible strategy, which meets the standard of green chemistry, is introduced for the synthesis of copper nanocrystals (Cu NCs) with olive oil as both reducing agent and capping agent. By changing the reaction parameters, the shape, size and surface structure of the Cu NCs can be well controlled. The obtained Cu nanocubes show excellent catalytic properties for the catalytic reduction of dyes and CO oxidation. Moreover, the prepared Cu nanocubes as substrates exhibit surface enhanced Raman scattering (SERS) activity for 4-mercaptopyridine (4-Mpy). Therefore, this facile route provides a useful platform for the fabrication of Cu NCs which have the potential to replace noble metals for certain applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr00412d

  2. Electronic structure studies of chemically synthesized MgFe2O4 nanoparticles

    NASA Astrophysics Data System (ADS)

    Singh, Jitendra Pal; Won, Sung Ok; Lim, Weon Cheol; Lee, Ik-Jae; Chae, K. H.

    2016-03-01

    For present work, magnesium ferrite nanoparticles were synthesized using nitrates of metal ions and citric acid. Crystallite size of these nanoparticles varies from 2.1 ± 0.1 to 62 ± 10 nm as annealing temperatures increases from 300 to 1200 °C. Mg K-edge near-edge X-ray absorption fine-structure spectra reflect the presence of Mg2+ ions in both tetrahedral (A-site) and octahedral (B-site) environment for nanoparticles synthesized at all temperatures. The integral area of spectral features of O K-edge spectra is associated with the change of unoccupied O p-projected density of states. Fe L-edge spectra envisage the presence of Fe3+ state in these nanoparticles. Observed changes in the electronic structure of these nanoparticles are discussed on the basis of cation migration from A-site to B-site, degree of crystallization, and unsaturated bonds at crystallite surface. Fe-O distances at A-site and B-site changes with annealing temperature.

  3. Chemical and Enzyme-Assisted Syntheses of Norbuprenorphine-3-β-D-Glucuronide

    PubMed Central

    Fan, Jinda; Brown, Sarah M.; Tu, Zhude; Kharasch, Evan D.

    2011-01-01

    Norbuprenorphine-3-β-D-glucuronide (nBPN-3-β-D-G, 1) is a major phase II metabolite of buprenorphine, a pharmaceutical used for the treatment of opioid addiction. The pharmacological activity of compound 1 is not clear because investigations have been limited by the lack of chemically pure, well characterized 1 in sufficient quantities for in vitro and in vivo experiments. This work describes two concise, new methods of synthesis of 1, a chemical and an enzyme-assisted synthesis. The chemical synthesis used a strategy based on a combination of Koenig-Knorr coupling and amino-silyl protection. The enzyme-assisted synthesis used dog liver to convert substrate norbuprenorphine (nBPN, 2) to 1. Both methods provided 1, characterized by 1H NMR and tandem mass spectrometry, with purity >96%. The fractional yield of the enzyme-assisted synthesis was greater than that of the chemical synthesis (67% vs 5.3%), but due to larger reaction volumes, the chemical synthesis afforded greater amounts of total 1. PMID:21434652

  4. SCRIPDB: a portal for easy access to syntheses, chemicals and reactions in patents.

    PubMed

    Heifets, Abraham; Jurisica, Igor

    2012-01-01

    The patent literature is a rich catalog of biologically relevant chemicals; many public and commercial molecular databases contain the structures disclosed in patent claims. However, patents are an equally rich source of metadata about bioactive molecules, including mechanism of action, disease class, homologous experimental series, structural alternatives, or the synthetic pathways used to produce molecules of interest. Unfortunately, this metadata is discarded when chemical structures are deposited separately in databases. SCRIPDB is a chemical structure database designed to make this metadata accessible. SCRIPDB provides the full original patent text, reactions and relationships described within any individual patent, in addition to the molecular files common to structural databases. We discuss how such information is valuable in medical text mining, chemical image analysis, reaction extraction and in silico pharmaceutical lead optimization. SCRIPDB may be searched by exact chemical structure, substructure or molecular similarity and the results may be restricted to patents describing synthetic routes. SCRIPDB is available at http://dcv.uhnres.utoronto.ca/SCRIPDB. PMID:22067445

  5. SCRIPDB: a portal for easy access to syntheses, chemicals and reactions in patents

    PubMed Central

    Heifets, Abraham; Jurisica, Igor

    2012-01-01

    The patent literature is a rich catalog of biologically relevant chemicals; many public and commercial molecular databases contain the structures disclosed in patent claims. However, patents are an equally rich source of metadata about bioactive molecules, including mechanism of action, disease class, homologous experimental series, structural alternatives, or the synthetic pathways used to produce molecules of interest. Unfortunately, this metadata is discarded when chemical structures are deposited separately in databases. SCRIPDB is a chemical structure database designed to make this metadata accessible. SCRIPDB provides the full original patent text, reactions and relationships described within any individual patent, in addition to the molecular files common to structural databases. We discuss how such information is valuable in medical text mining, chemical image analysis, reaction extraction and in silico pharmaceutical lead optimization. SCRIPDB may be searched by exact chemical structure, substructure or molecular similarity and the results may be restricted to patents describing synthetic routes. SCRIPDB is available at http://dcv.uhnres.utoronto.ca/SCRIPDB. PMID:22067445

  6. Chemical and enzyme-assisted syntheses of norbuprenorphine-3-β-D-glucuronide.

    PubMed

    Fan, Jinda; Brown, Sarah M; Tu, Zhude; Kharasch, Evan D

    2011-04-20

    Norbuprenorphine-3-β-d-glucuronide (nBPN-3-β-d-G, 1) is a major phase II metabolite of buprenorphine, a pharmaceutical used for the treatment of opioid addiction. The pharmacological activity of compound 1 is not clear because investigations have been limited by the lack of chemically pure, well characterized 1 in sufficient quantities for in vitro and in vivo experiments. This work describes two concise, new methods of synthesis of 1, a chemical and an enzyme-assisted synthesis. The chemical synthesis used a strategy based on a combination of Koenig-Knorr coupling and amino-silyl protection. The enzyme-assisted synthesis used dog liver to convert the substrate norbuprenorphine (nBPN, 2) to 1. Both methods provided 1, characterized by (1)H NMR and tandem mass spectrometry, with purity >96%. The fractional yield of the enzyme-assisted synthesis was greater than that of the chemical synthesis (67% vs 5.3%), but due to larger reaction volumes, the chemical synthesis afforded greater amounts of total 1. PMID:21434652

  7. Exploring the chemical sensitivity of a carbon nanotube/green tea composite.

    PubMed

    Chen, Yanan; Lee, Yang Doo; Vedala, Harindra; Allen, Brett L; Star, Alexander

    2010-11-23

    Single-walled carbon nanotubes (SWNTs) possess unique electronic and physical properties, which make them very attractive for a wide range of applications. In particular, SWNTs and their composites have shown a great potential for chemical and biological sensing. Green tea, or more specifically its main antioxidant component, epigallocatechin gallate (EGCG), has been found to disperse SWNTs in water. However, the chemical sensitivity of this SWNT/green tea (SWNT/EGCG) composite remained unexplored. With EGCG present, this SWNT composite should have strong antioxidant properties and thus respond to reactive oxygen species (ROS). Here we report on fabrication and characterization of SWNT/EGCG thin films and the measurement of their relative conductance as a function of H(2)O(2) concentrations. We further investigated the sensing mechanism by Fourier transform infrared (FTIR) spectroscopy and field-effect transistor measurements (FET). We propose here that the response to H(2)O(2) arises from the oxidation of EGCG in the composite. These findings suggest that SWNT/green tea composite has a great potential for developing simple resistivity-based sensors. PMID:21043457

  8. Exploring the Chemical Sensitivity of a Carbon Nanotube/Green Tea Composite

    PubMed Central

    Chen, Yanan; Lee, Yang Doo; Vedala, Harindra; Allen, Brett L.; Star, Alexander

    2010-01-01

    Single-walled carbon nanotubes (SWNTs) possess unique electronic and physical properties, which make them very attractive for a wide range of applications. In particular, SWNTs and their composites have shown a great potential for chemical and biological sensing. Green tea, or more specifically its main antioxidant component, epigallocatechin gallate (EGCG), has been found to disperse SWNTs in water. However, the chemical sensitivity of this SWNT/green tea (SWNT/EGCG) composite remained unexplored. With EGCG present, this SWNT composite should have strong antioxidant properties and thus respond to reactive oxygen species (ROS). Here we report on fabrication and characterization of SWNT/EGCG thin films and the measurement of their relative conductance as a function of H2O2 concentrations. We further investigated the sensing mechanism by Fourier-transform infrared (FTIR) spectroscopy and field-effect transistor measurements (FET). We propose here that the response to H2O2 arises from the oxidation of EGCG in the composite. These findings suggest that SWNT/green tea composite has a great potential for developing simple resistivity-based sensors. PMID:21043457

  9. ON THE OXYGEN AND NITROGEN CHEMICAL ABUNDANCES AND THE EVOLUTION OF THE 'GREEN PEA' GALAXIES

    SciTech Connect

    Amorin, Ricardo O.; Perez-Montero, Enrique; Vilchez, J. M. E-mail: epm@iaa.e

    2010-06-01

    We have investigated the oxygen and nitrogen chemical abundances in extremely compact star-forming galaxies (SFGs) with redshifts between {approx}0.11 and 0.35, popularly referred to as 'green peas'. Direct and strong-line methods sensitive to the N/O ratio applied to their Sloan Digital Sky Survey (SDSS) spectra reveal that these systems are genuine metal-poor galaxies, with mean oxygen abundances {approx}20% solar. At a given metallicity these galaxies display systematically large N/O ratios compared to normal galaxies, which can explain the strong difference between our metallicities measurements and previous ones. While their N/O ratios follow the relation with stellar mass of local SFGs in the SDSS, we find that the mass-metallicity relation of the 'green peas' is offset {approx_gt}0.3 dex to lower metallicities. We argue that recent interaction-induced inflow of gas, possibly coupled with a selective metal-rich gas loss, driven by supernova winds, may explain our findings and the known galaxy properties, namely high specific star formation rates, extreme compactness, and disturbed optical morphologies. The 'green pea' galaxy properties seem to be uncommon in the nearby universe, suggesting a short and extreme stage of their evolution. Therefore, these galaxies may allow us to study in great detail many processes, such as starburst activity and chemical enrichment, under physical conditions approaching those in galaxies at higher redshifts.

  10. Correlation between magnetic spin structure and the three-dimensional geometry in chemically synthesized nanoscale magnetite rings

    NASA Astrophysics Data System (ADS)

    Eltschka, M.; Kläui, M.; Rüdiger, U.; Kasama, T.; Cervera-Gontard, L.; Dunin-Borkowski, R. E.; Luo, F.; Heyderman, L. J.; Jia, C.-J.; Sun, L.-D.; Yan, C.-H.

    2008-06-01

    The correlation between magnetic spin structure and geometry in nanoscale chemically synthesized Fe3O4 rings has been investigated by transmission electron microscopy. We find primarily the flux closure vortex states but in rings with thickness variations, an effective stray field occurs. Using tomography, we determine the complete three-dimensional geometries of thicker rings. A direct correlation between the geometry and the magnetization which points out of plane in the thickest parts of the ring yielding an intermediate magnetic state between the vortex state and the tube state is found. The interaction between exchange coupled rings leads to antiparallel vortex states and extended onion states.

  11. ZnO/SnO2 nanoflower based ZnO template synthesized by thermal chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Sin, N. D. Md.; Amalina, M. N.; Ismail, Ahmad Syakirin; Shafura, A. K.; Ahmad, Samsiah; Mamat, M. H.; Rusop, M.

    2016-07-01

    The ZnO/SnO2 nanoflower like structures was grown on a glass substrate deposited with seed layer using thermal chemical vapor deposition (CVD) with combining two source materials. The ZnO/SnO2 nanoflower like structures had diameter in the range 70 to 100nm. The atomic percentage of ZnO nanoparticle , SnO2 nanorods and ZnO/SnO2 nanoflower was taken using EDS. Based on the FESEM observations, the growth mechanism is applied to describe the growth for the synthesized nanostructures.

  12. Learning, memorizing and apparent forgetting of chemical cues from new predators by Iberian green frog tadpoles.

    PubMed

    Gonzalo, Adega; López, Pilar; Martín, José

    2009-09-01

    Many antipredator adaptations are induced by the prey's ability to recognize chemical cues from predators. However, predator recognition often requires learning by prey individuals. Iberian green frog tadpoles (Pelophylax perezi) have the ability to learn new potential predators. Here, we tested the memory capabilities of Iberian green frog tadpoles. We conditioned tadpoles with chemicals cues from a non-predatory fish in conjunction with conspecific alarm cues, and examined whether tadpoles retained their conditioned response (reduction of activity level). We found that conditioned tadpoles reduced their activity levels in subsequent exposures to the non-predatory fish cues alone. Tadpoles were able to remember this association and reduced movement rate at least for 9 days after. The ability to learn and memorize potential predators may be especially important for the survivorship of prey species that are likely to find a high variety of predators. However, after those 9 days, there was a lack of response to the non-predatory fish cues alone in the absence of reinforcement. This could be explained if tadpoles behave according to the threat-sensitive predator avoidance hypothesis, and the perceived risk to the learning cue diminished over time, or it could be due to an apparent forgetting process to avoid non-adaptative responses to chemical cues of non-dangerous species that were randomly paired with alarm cues. Thus, this study demonstrates that green frog tadpoles in the absence of reinforcement remember the chemical cues of a learned predator only for a limited time that may be adaptative in a threat-sensitive context. PMID:19449191

  13. Synthesis, characterization, and electrochemical studies of chemically synthesized NaFePO{sub 4}

    SciTech Connect

    Sun, Ann; Beck, Faith R; Haynes, Daniel; Poston, James A; Narayanana, S R; Kumta, Prashant N; Manivannan, A

    2012-12-01

    NaFePO{sub 4} is a naturally occurring mineral known as maricite. This compound has not been well characterized or examined for its potential use in battery applications. In the present study, NaFePO{sub 4} has been synthesized via the Pechini process with the resulting sample being characterized by X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Electrochemical properties have been investigated for possible application as a cathode in sodium-ion batteries. Electrodes of these materials were tested in coin cells using LiPF{sub 6} as the electrolyte and lithium metal as the counter electrode. Constant current cycling, cyclic voltammetry, and in situ frequency response analyses were performed. The results obtained demonstrate constant capacity or progressive increase in capacity with the consistently low internal resistance exhibited over consecutive cycles indicating possible application as a lithium analog in Na-ion batteries.

  14. Optical and electrical properties of undoped and boron doped zinc oxide synthesized by chemical route

    SciTech Connect

    Bhattacharjee, Snigdha; Basu, Moumita; Roy, Asim

    2015-08-28

    We have synthesized and studied the boron doped ZnO nanostructure thin films. The crystallinity of undoped and boron (B) doped ZnO (BZO) has been studied from XRD results. Using the Debye-Scherrer Formula, the grain size has been evaluated, which was found to decrease with increased doping concentration. The optical and electrical properties of (1, 3, 5 wt%) B-doped ZnO (BZO) has been investigated with reference to the undoped counterpart. The UV-VIS spectroscopic analysis revealed that the transmittance for undoped ZnO is maximum and it decreases with doping up to 3% but increases for 5% BZO. The dark as well as photo current–voltage (I–V) characteristics have been investigated in details and the changes occurred in the I-V characteristics with doping concentration as well as under illumination are also quite significant.

  15. Phthalic acid chemical probes synthesized for protein-protein interaction analysis.

    PubMed

    Liang, Shih-Shin; Liao, Wei-Ting; Kuo, Chao-Jen; Chou, Chi-Hsien; Wu, Chin-Jen; Wang, Hui-Min

    2013-01-01

    Plasticizers are additives that are used to increase the flexibility of plastic during manufacturing. However, in injection molding processes, plasticizers cannot be generated with monomers because they can peel off from the plastics into the surrounding environment, water, or food, or become attached to skin. Among the various plasticizers that are used, 1,2-benzenedicarboxylic acid (phthalic acid) is a typical precursor to generate phthalates. In addition, phthalic acid is a metabolite of diethylhexyl phthalate (DEHP). According to Gene_Ontology gene/protein database, phthalates can cause genital diseases, cardiotoxicity, hepatotoxicity, nephrotoxicity, etc. In this study, a silanized linker (3-aminopropyl triethoxyslane, APTES) was deposited on silicon dioxides (SiO2) particles and phthalate chemical probes were manufactured from phthalic acid and APTES-SiO2. These probes could be used for detecting proteins that targeted phthalic acid and for protein-protein interactions. The phthalic acid chemical probes we produced were incubated with epithelioid cell lysates of normal rat kidney (NRK-52E cells) to detect the interactions between phthalic acid and NRK-52E extracted proteins. These chemical probes interacted with a number of chaperones such as protein disulfide-isomerase A6, heat shock proteins, and Serpin H1. Ingenuity Pathways Analysis (IPA) software showed that these chemical probes were a practical technique for protein-protein interaction analysis. PMID:23797655

  16. Rapid Prototyping of Chemical Microsensors Based on Molecularly Imprinted Polymers Synthesized by Two-Photon Stereolithography.

    PubMed

    Gomez, Laura Piedad Chia; Spangenberg, Arnaud; Ton, Xuan-Anh; Fuchs, Yannick; Bokeloh, Frank; Malval, Jean-Pierre; Tse Sum Bui, Bernadette; Thuau, Damien; Ayela, Cédric; Haupt, Karsten; Soppera, Olivier

    2016-07-01

    Two-photon stereolithography is used for rapid prototyping of submicrometre molecularly imprinted polymer-based 3D structures. The structures are evaluated as chemical sensing elements and their specific recognition properties for target molecules are confirmed. The 3D design capability is exploited and highlighted through the fabrication of an all-organic molecularly imprinted polymeric microelectromechanical sensor. PMID:27145145

  17. Green-synthesized silver nanoparticles as a novel control tool against dengue virus (DEN-2) and its primary vector Aedes aegypti.

    PubMed

    Sujitha, Vasu; Murugan, Kadarkarai; Paulpandi, Manickam; Panneerselvam, Chellasamy; Suresh, Udaiyan; Roni, Mathath; Nicoletti, Marcello; Higuchi, Akon; Madhiyazhagan, Pari; Subramaniam, Jayapal; Dinesh, Devakumar; Vadivalagan, Chithravel; Chandramohan, Balamurugan; Alarfaj, Abdullah A; Munusamy, Murugan A; Barnard, Donald R; Benelli, Giovanni

    2015-09-01

    Dengue is an arthropod-borne viral infection mainly vectored through the bite of Aedes mosquitoes. Recently, its transmission has strongly increased in urban and semi-urban areas of tropical and sub-tropical regions worldwide, becoming a major international public health concern. There is no specific treatment for dengue. Its prevention and control solely depends on effective vector control measures. In this study, we proposed the green-synthesis of silver nanoparticles (AgNP) as a novel and effective tool against the dengue serotype DEN-2 and its major vector Aedes aegypti. AgNP were synthesized using the Moringa oleifera seed extract as reducing and stabilizing agent. AgNP were characterized using a variety of biophysical methods including UV-vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and sorted for size categories. AgNP showed in vitro antiviral activity against DEN-2 infecting vero cells. Viral titer was 7 log10 TCID50/ml in control (AgNP-free), while it dropped to 3.2 log10 TCID50/ml after a single treatment with 20 μl/ml of AgNP. After 6 h, DEN-2 yield was 5.8 log10 PFU/ml in the control, while it was 1.4 log10 PFU/ml post-treatment with AgNP (20 μl/ml). AgNP were highly effective against the dengue vector A. aegypti, with LC50 values ranging from 10.24 ppm (I instar larvae) to 21.17 ppm (pupae). Overall, this research highlighted the concrete potential of green-synthesized AgNP in the fight against dengue and its primary vector A. aegypti. Further research on structure-activity relationships of AgNP against other dengue serotypes is urgently required. PMID:26063530

  18. Sequestered and Synthesized Chemical Defenses in the Poison Frog Melanophryniscus moreirae.

    PubMed

    Jeckel, Adriana M; Grant, Taran; Saporito, Ralph A

    2015-05-01

    Bufonid poison frogs of the genus Melanophryniscus contain alkaloid-based chemical defenses that are derived from a diet of alkaloid-containing arthropods. In addition to dietary alkaloids, bufadienolide-like compounds and indolealkylamines have been identified in certain species of Melanophryniscus. Our study reports, for the first time, the co-occurrence of large quantities of both alkaloids sequestered from the diet and an endogenously biosynthesized indolalkylamine in skin secretions from individual specimens of Melanophryniscus moreirae from Brazil. GC/MS analysis of 55 individuals of M. moreirae revealed 37 dietary alkaloids and the biosynthesized indolealkylamine bufotenine. On average, pumiliotoxin 267C, bufotenine, and allopumilitoxin 323B collectively represent ca. 90 % of the defensive chemicals present in an individual. The quantity of defensive chemicals differed between sexes, with males possessing significantly less dietary alkaloid and bufotenine than females. Most of the dietary alkaloids have structures with branched-chains, indicating they are likely derived from oribatid mites. The ratio of bufotenine:alkaloid quantity decreased with increasing quantities of dietary alkaloids, suggesting that M. moreirae might regulate bufotenine synthesis in relation to sequestration of dietary alkaloids. PMID:25902958

  19. SHI induced defects in chemically synthesized graphene oxide for hydrogen storage applications

    NASA Astrophysics Data System (ADS)

    Sharma, Preetam K.; Sharma, Vinay; Rajaura, Rajveer Singh; Srivastava, Subodh; Sharma, S. S.; Singh, M.; Vijay, Y. K.

    2016-05-01

    Graphene, due to its unique properties arising from the single carbon layer, is a potential candidate for applications in a variety of fields including sensors, photovoltaics and energy storage. The atomic structure and morphology of the carbon nanomaterials especially graphene can be tailored by energetic ionic irradiation. As graphene sheet is very stable, the surface have less reactivity as compared to the edges of the sheets. By surface modification with energetic ion-beams additional dangling bonds can be formed to enhance the surface activity of the graphene film which could be exploited in a variety of applications. In the present work, graphene oxide was synthesized by improved Hummers' Method. The irradiation was done with Ag+ ions carrying energy 100 MeV with the fluence of 3×1013. Raman spectrum of graphene irradiated by Ag+ beam shows additional disordered peaks of D' and D+G bands. There is also a decrease in the intensity of D band. AFM images depict the increase in the surface roughness of the films. This can be attributed to the increase in the defects in the flakes and intermixing of adjacent layers by irradiation.

  20. Green in-situ synthesized silver nanoparticles embedded in bacterial cellulose nanopaper as a bionanocomposite plasmonic sensor.

    PubMed

    Pourreza, Nahid; Golmohammadi, Hamed; Naghdi, Tina; Yousefi, Hossein

    2015-12-15

    Herein, we introduce a new strategy for green, in-situ generation of silver nanoparticles using flexible and transparent bacterial cellulose nanopapers. In this method, adsorbed silver ions on bacterial cellulose nanopaper are reduced by the hydroxyl groups of cellulose nanofibers, acting as the reducing agent producing a bionanocomposite "embedded silver nanoparticles in transparent nanopaper" (ESNPs). The fabricated ESNPs were investigated and characterized by field emission scanning electron microscopy (FE-SEM), UV-visible spectroscopy (UV-vis), Fourier-transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and energy-dispersive X-ray spectroscopy (EDX). The important parameters affecting the ESNPs were optimized during the fabrication of specimens. The resulting ESNPs were used as a novel and sensitive probe for the optical sensing of cyanide ion (CN(-)) and 2-mercaptobenzothiazole (MBT) in water samples with satisfactory results. The change in surface plasmon resonance absorption intensity of ESNPs was linearly proportional to the concentration in the range of 0.2-2.5 µg mL(-1) and 2-110 µg mL(-1) with a detection limit of 0.012 µg mL(-1) and 1.37 µg mL(-1) for CN(-) and MBT, respectively. PMID:26159156

  1. Density Functional Theory for Green Chemical Catalyst Supported on S-Terminated GaN(0001)

    NASA Astrophysics Data System (ADS)

    Yokoyama, Mami; Tsukamoto, Shiro; Ishii, Akira

    2011-12-01

    A novel function of nitried-based semiconductor is successfully developed for organic synthesis, in which palladium supported on the surface of S-terminated GaN(0001) serves as a unique green chemical catalyst. In this study we determined the structure of Pd-catalyst supported on S-terminated GaN(0001) surface by means of the density functional theory (DFT) within a Local Density Approximation (LDA). The important role of S on the case of GaN substrate is to make the number of the valence electron to be close to 0, it happened same way for GaAs substrate.

  2. Activation of chemicals into mutagens by green plants: a preliminary discussion.

    PubMed Central

    Plewa, M J

    1978-01-01

    This paper is a review of recent studies that demonstrate the activation of chemicals (especially pesticides into mutagens by green plants. Such activation of pesticides may be hazardous to the public health because of their widespread use in agriculture and the current lack of information that exists about such processes. The mutagenic properties of the s-triazine herbicides (atrazine, simazine, and cyanazine) as exhibited in various assay systems are discussed. In vivo, in vitro, and in situ plant assays are presented, and the maize wx locus assay is discussed. PMID:367774

  3. Role of nanocrystallinity on the chemical ordering of CoxPt100-x nanocrystals synthesized by wet chemistry

    DOE PAGESBeta

    Cordeiro, Marco; Kameche, Farid; Ngo, Anh -Tu; Salzemann, Caroline; Sutter, Eli; Petit, Christophe

    2015-03-17

    CoxPt100–x nanoalloys have been synthesized by two different chemical processes either at high or at low temperature. Their physical properties and the order/disorder phase transition induced by annealing have been investigated depending on the route of synthesis. It is demonstrated that the chemical synthesis at high temperature allows stabilization of the fcc structure of the native nanoalloys while the soft chemical approach yields mainly poly or non crystalline structure. As a result the approach of the order/disorder phase transition is strongly modified as observed by high-resolution transmission electron microscopy (HR-TEM) studies performed during in situ annealing of the different nanoalloys.more » The control of the nanocrystallinity leads to significant decrease in the chemical ordering temperature as the ordered structure is observed at temperatures as low as 420 °C. Furthermore, this in turn preserves the individual nanocrystals and prevents their coalescence usually observed during the annealing necessary for the transition to an ordered phase.« less

  4. Evaluating the "greenness" of chemical processes and products in the pharmaceutical industry--a green metrics primer.

    PubMed

    Jiménez-González, Concepción; Constable, David J C; Ponder, Celia S

    2012-02-21

    This tutorial review presents an overview of the main metrics that have been used to test and compare the 'greenness' of processes and products, primarily in the pharmaceutical industry. The green metrics cover areas of resources, materials, processing, cleaning, life cycle assessment, renewability, amongst others. Application examples of these metrics are also presented to illustrate key points and concepts. PMID:22076593

  5. Chemical and biomimetic total syntheses of natural and engineered MCoTI cyclotides.

    PubMed

    Thongyoo, Panumart; Roqué-Rosell, Núria; Leatherbarrow, Robin J; Tate, Edward W

    2008-04-21

    The naturally-occurring cyclic cystine-knot microprotein trypsin inhibitors MCoTI-I and MCoTI-II have been synthesised using both thia-zip native chemical ligation and a biomimetic strategy featuring chemoenzymatic cyclisation by an immobilised protease. Engineered analogues have been produced containing a range of substitutions at the P1 position that redirect specificity towards alternative protease targets whilst retaining excellent to moderate affinity. Furthermore, we report an MCoTI analogue that is a selective low-microM inhibitor of foot-and-mouth-disease virus (FMDV) 3C protease, the first reported peptide-based inhibitor of this important viral enzyme. PMID:18385853

  6. Synthesis and optical studies of chemically synthesized PPy/Al2O3 nanocomposites

    NASA Astrophysics Data System (ADS)

    Bahadur, Indra; Mishra, Sheo K.; Tripathi, Akhilesh; Shukla, R. K.

    2016-05-01

    In the present work, we have synthesised pure and 2wt% Al2O3 doped PPy by the chemical oxidation method. XRD patterns of 2wt% Al2O3 doped PPy shows several broad peaks while pure PPy shows only one single peak indicating poor crystalline phase of PPy. FTIR spectra confirm the formation of PPy and also suggest that doping of Al2O3 in PPy does not affect its structure. PL shows several emission peaks for both samples located at ˜365 nm with two shoulders at ˜473 nm and ˜533 nm. The further synthesis and properties study is under investigation.

  7. Studies towards the development of chemically synthesized non-radioactive biotinylated nucleic acid hybridization probes.

    PubMed Central

    Al-Hakim, A H; Hull, R

    1986-01-01

    Non-radioactive nucleic acid hybridization probes have been constructed in which the reporter group is long chain biotin chemically linked to a basic macromolecule (histone H1, cytochrome C or polyethyleneimine). The modified basic macromolecule which carries many biotin residues can, in turn, be covalently linked to nucleic acids (DNA) via the bifunctional cross-linking reagents, glutaraldehyde, 1,2,7,8-diepoxyoctane, bis (succinimidyl) suberate or bis (sulfonosuccinimidyl) suberate. This provides a very sensitive probe by which as little as between 10-50fg of target DNA can be visualized using dot-blot hybridization procedures in conjunction with avidin or streptavidin enzyme conjugates. PMID:3027670

  8. Nonlinear optical characterization of ZnS thin film synthesized by chemical spray pyrolysis method

    SciTech Connect

    G, Sreeja V; Anila, E. I. R, Reshmi John, Manu Punnan; V, Sabitha P; Radhakrishnan, P.

    2014-10-15

    ZnS thin film was prepared by Chemical Spray Pyrolysis (CSP) method. The sample was characterized by X-ray diffraction method and Z scan technique. XRD pattern showed that ZnS thin film has hexagonal structure with an average size of about 5.6nm. The nonlinear optical properties of ZnS thin film was studied by open aperture Z-Scan technique using Q-switched Nd-Yag Laser at 532nm. The Z-scan plot showed that the investigated ZnS thin film has saturable absorption behavior. The nonlinear absorption coefficient and saturation intensity were also estimated.

  9. Nonlinear optical characterization of ZnS thin film synthesized by chemical spray pyrolysis method

    NASA Astrophysics Data System (ADS)

    G, Sreeja V.; V, Sabitha P.; Anila, E. I.; R, Reshmi; John, Manu Punnan; Radhakrishnan, P.

    2014-10-01

    ZnS thin film was prepared by Chemical Spray Pyrolysis (CSP) method. The sample was characterized by X-ray diffraction method and Z scan technique. XRD pattern showed that ZnS thin film has hexagonal structure with an average size of about 5.6nm. The nonlinear optical properties of ZnS thin film was studied by open aperture Z-Scan technique using Q-switched Nd-Yag Laser at 532nm. The Z-scan plot showed that the investigated ZnS thin film has saturable absorption behavior. The nonlinear absorption coefficient and saturation intensity were also estimated.

  10. Comprehensive optical studies on SnS layers synthesized by chemical bath deposition

    NASA Astrophysics Data System (ADS)

    Gedi, Sreedevi; Minnam Reddy, Vasudeva Reddy; Park, Chinho; Chan-Wook, Jeon; Ramakrishna Reddy, K. T.

    2015-04-01

    A simple non-vacuum and cost effective wet chemical technique, chemical bath deposition was used to prepare tin sulphide (SnS) layers on glass substrates. The layers were formed by varying bath temperature in the range, 40-80 °C, keeping other deposition parameters as constant. An exhaustive investigation on their optical properties with bath temperature was made using the transmittance and reflectance measurements. The absorption coefficient was evaluated from the optical transmittance data utilizing Lambert's principle and is >104 cm-1 for all the as-prepared layers. The energy band gap of the layers was determined from the differential reflectance spectra that varied from 1.41 eV to 1.30 eV. Consequently, refractive index and extinction coefficient were obtained from Pankov relations and dispersion constants were calculated using Wemple-Didomenico method. In addition, other optical parameters such as the optical conductivity, dielectric constants, dissipation factor, high frequency dielectric constant and relaxation time were also calculated. Finally electrical parameters such as resistivity, carrier mobility and carrier density of as-prepared layers were estimated using optical data. A detailed analysis of the dependence of all above mentioned parameters on bath temperature is reported and discussed for a clean understanding of electronic characteristics of SnS layers.

  11. Superior Mobility in Chemical Vapor Deposition Synthesized Graphene by Grain Size Engineering

    NASA Astrophysics Data System (ADS)

    Petrone, Nicholas; Dean, Cory; Meric, Inanc; van der Zande, Arend; Huang, Pinshane; Wang, Lei; Muller, David; Shepard, Kenneth; Hone, James

    2012-02-01

    Chemical vapor deposition (CVD) offers a promising method to produce large-area films of graphene, crucial for commercial realization of graphene-based applications. However, electron transport in CVD grown graphene has continued to fall short of the performance demonstrated by graphene derived from mechanical exfoliation. Lattice defects and grain boundaries developed during growth, structural defects and chemical contamination introduced during transfer, and charged scatterers present in sub-optimal dielectric substrates have all been identified as sources of disorder in CVD grown graphene devices. We grow CVD graphene and fabricate field-effect transistors, attempting to minimize potential sources of disorder. We reduce density of grain boundaries in CVD graphene by controlling domain sizes up to 250 microns. By transferring CVD graphene onto h-BN utilizing a dry-transfer method, we minimize trapped charges at the interface between graphene and in the underlying substrate. We report field-effect mobilities up to 110,000 cm2V-1s-1 and oscillations in magnetotransport measurements below 1 T, confirming the high quality and low disorder in our CVD graphene devices.

  12. Chemically and biologically synthesized CPP-modified gelonin for enhanced anti-tumor activity.

    PubMed

    Shin, Meong Cheol; Zhang, Jian; David, Allan E; Trommer, Wolfgang E; Kwon, Young Min; Min, Kyoung Ah; Kim, Jin H; Yang, Victor C

    2013-11-28

    The ineffectiveness of small molecule drugs against cancer has generated significant interest in more potent macromolecular agents. Gelonin, a plant-derived toxin that inhibits protein translation, has attracted much attention in this regard. Due to its inability to internalize into cells, however, gelonin exerts only limited tumoricidal effect. To overcome this cell membrane barrier, we modified gelonin, via both chemical conjugation and genetic recombination methods, with low molecular weight protamine (LMWP), a cell-penetrating peptide (CPP) which was shown to efficiently ferry various cargoes into cells. Results confirmed that gelonin-LMWP chemical conjugate (cG-L) and recombinant gelonin-LMWP chimera (rG-L) possessed N-glycosidase activity equivalent to that of unmodified recombinant gelonin (rGel); however, unlike rGel, both gelonin-LMWPs were able to internalize into cells. Cytotoxicity studies further demonstrated that cG-L and rG-L exhibited significantly improved tumoricidal effects, with IC50 values being 120-fold lower than that of rGel. Moreover, when tested against a CT26 s.c. xenograft tumor mouse model, significant inhibition of tumor growth was observed with rG-L doses as low as 2 μg/tumor, while no detectable therapeutic effects were seen with rGel at 10-fold higher doses. Overall, this study demonstrated the potential of utilizing CPP-modified gelonin as a highly potent anticancer drug to overcome limitations of current chemotherapeutic agents. PMID:23973813

  13. Aristolochia indica green-synthesized silver nanoparticles: A sustainable control tool against the malaria vector Anopheles stephensi?

    PubMed

    Murugan, Kadarkarai; Labeeba, Mohammed Aamina; Panneerselvam, Chellasamy; Dinesh, Devakumar; Suresh, Udaiyan; Subramaniam, Jayapal; Madhiyazhagan, Pari; Hwang, Jiang-Shiou; Wang, Lan; Nicoletti, Marcello; Benelli, Giovanni

    2015-10-01

    Malaria is a life-threatening disease caused by parasites transmitted to people and animals through the bites of infected mosquitoes. We biosynthesized silver nanoparticles (AgNP) using Aristolochia indica extract as reducing and stabilizing agent. AgNP were characterized by UV-vis spectroscopy, FTIR, SEM, EDX and XRD. In laboratory, LC50 of A. indica extract against Anopheles stephensi ranged from 262.66 (larvae I) to 565.02 ppm (pupae). LC50 of AgNP against A. stephensi ranged from 3.94 (larvae I) to 15.65 ppm (pupae). In the field, the application of A. indica extract and AgNP (10 × LC50) leads to 100% larval reduction after 72 h. In laboratory, 24-h predation efficiency of Diplonychus indicus against A. stephensi larvae was 33% (larvae II) and 57% (larvae III). In AgNP-contaminated environment (1 ppm), it was 45.5% (larvae II) and 71.75% (larvae III). Overall, A. indica-synthesized AgNP may be considered as newer and safer control tools against Anopheles vectors. PMID:26412532

  14. Chemical and physical properties of high-yield alkaline sulfite green liquor

    SciTech Connect

    Sell, N.J.; Norman, J.C. . Natural and Applied Sciences)

    1993-11-01

    The majority of sodium sulfite pulping liquor recovery systems are based on the reductive burning of the spent liquor, followed by acidification of the resulting smelt solution by CO[sub 2]. This study investigated a number of the physical and chemical properties of the resulting green liquor which might be relevant to the optimum design of this type of sulfite and carbonate recovery system for an alkaline sulfite high-yield process. CO[sub 2] gas does generate H[sub 2]S when bubbled through green liquor; however, a large amount of solid soon is formed. Continuing the flow leads to increased amounts of H[sub 2]S, but the ratio of H[sub 2]S to CO[sub 2] remains less than 1.0. Solutions more highly concentrated in Na[sub 2]S absorb relatively more CO[sub 2], regardless of the ratios of H[sub 2]S to CO[sub 2] in the initial gas stream. The percentage of H[sub 2]S released increases with increasing Na[sub 2]S concentration. Stripping the green liquor with inert gas, steam, or vacuum does not improve the H[sub 2]S removal efficiency. The maximum CO[sub 2] pressure can be generated by decomposing pure 6 M NaHCO[sub 3]. If the starting material is a bicarbonate/carbonate mixture, conversion is incomplete and a portion of the NaHCO[sub 3] forms a dead load.

  15. The green synthesis, characterization, and evaluation of the biological activities of silver nanoparticles synthesized from Leptadenia reticulata leaf extract

    NASA Astrophysics Data System (ADS)

    Kumara Swamy, M.; Sudipta, K. M.; Jayanta, K.; Balasubramanya, S.

    2015-01-01

    Biosynthesis of silver nanoparticles (Ag Nps) was carried out using methanol leaves extract of L. reticulata. Ag Nps were characterized based on the observations of UV-visible spectroscopy, transmission electron microscopy, and X-ray diffraction (XRD) analysis. These Ag Nps were tested for antimicrobial activity by agar well diffusion method against different pathogenic microorganisms and antioxidant activity was performed using DPPH assay. Further, the in vitro cytotoxic effects of Ag Nps were screened against HCT15 cancer cell line and viability of tumor cells was confirmed using MTT ((3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, a yellow tetrazole)) assay. The nuclear condensation was studied using the propidium iodide-staining method. The color change from green to dark brown and the absorbance peak at about 420 nm indicated the formation of nanoparticles. XRD pattern showed characteristic peaks indexed to the crystalline planes (111), (200) and (220) of face-centered cubic silver. The nanoparticles were of spherical shape with varying sizes ranging from 50 to 70 nm. Biosynthesized Ag Nps showed potent antibacterial activity and effective radical scavenging activity. MTT assay revealed a dose-dependent decrease in cell viability. Microscopic observations showed distinct cellular morphological changes indicating unhealthy cells, whereas the control appeared normal. Increase in the number of propidium iodide positive cells were observed in maximum concentration. Methanolic leaf extract of L. reticulata acts as an excellent capping agent for the formation of silver nanoparticles and demonstrates immense biological activities. Hence, these Ag NPs can be used as antibacterial, antioxidant as well as cytotoxic agent in treating many medical complications.

  16. Characterization of green synthesized nano-formulation (ZnO-A. vera) and their antibacterial activity against pathogens.

    PubMed

    Qian, Yiguang; Yao, Jun; Russel, Mohammad; Chen, Ke; Wang, Xiaoyu

    2015-03-01

    The application of nanotechnology in medicine has recently been a breakthrough in therapeutic drugs formulation. This paper presents the structural and optical characterization of a new green nano-formulation (ZnO-Aloe vera) with considerable antibacterial activity against pathogenic bacteria. Its particle structure, size and morphology were characterized by XRD, TEM and SEM. And optical absorption spectra and photoluminescence were measured synchronously. Their antibacterial activity against Escherichia coli and Staphylococcus aureus was also investigated using thermokinetic profiling and agar well diffusion method. The nano-formulation is spherical shape and hexagonal with a particle size ranging from 25 to 65 nm as well as an increased crystallite size of 49 nm. For antibacterial activity, the maximum inhibition zones of ZnO and ZnO+A. vera are 18.33 and 26.45 mm for E. coli, 22.11 and 28.12 mm for S. aureus (p<0.05). Considering Pmax, Qt and k, ZnO+A. vera nano-formulation has a significant (p < 0.05) antibacterial effect against S. aureus almost at all concentration and against E. coli at 15 and 25mg/L. ZnO+A. vera nano-formulation is much more toxic against S. aureus than E. coli, with an IC50 of 13.12 mg/L and 21.31 mg/L, respectively. The overall results reveal that the ZnO-A. vera nano-formulation has good surface energy, crystallinity, transmission, and enriched antibacterial activities. Their antibacterial properties are possibly relevant to particle size, microstructural ionization, the crystal formation and the Gram property of pathogens. This ZnO-A. vera nano-formulation could be utilized effectively as a spectral and significant antibacterial agent for pathogens in future medical and environmental concerns. PMID:25723342

  17. Is Chemically Synthesized Graphene ‘Really’ a Unique Substrate for SERS and Fluorescence Quenching?

    NASA Astrophysics Data System (ADS)

    Sil, Sanchita; Kuhar, Nikki; Acharya, Somnath; Umapathy, Siva

    2013-11-01

    We demonstrate observation of Raman signals of different analytes adsorbed on carbonaceous materials, such as, chemically reduced graphene, graphene oxide (GO), multi-walled carbon nanotube (MWCNT), graphite and activated carbon. The analytes selected for the study were Rhodamine 6G (R6G) (in resonant conditions), Rhodamine B (RB), Nile blue (NBA), Crystal Violet (CV) and acetaminophen (paracetamol). All the analytes except paracetamol absorb and fluoresce in the visible region. In this article we provide experimental evidence of the fact that observation of Raman signals of analytes on such carbonaceous materials are more due to resonance effect, suppression of fluorescence and efficient adsorption and that this property in not unique to graphene or nanotubes but prevalent for various type of carbon materials.

  18. with very high saturation magnetization and negligible dielectric loss synthesized via a soft chemical route

    NASA Astrophysics Data System (ADS)

    Mukherjee, S.; Pradip, S.; Mishra, A. K.; Das, D.

    2014-07-01

    Materials with high saturation magnetization and low dielectric loss are in great demand due to the great boom in communication industry. In this paper, we report the synthesis of nanoferrites with the generic formula Zn x Ni(1- x)Fe2O4 ( x = 0.0, 0.1, 0.3 and 0.5) through chemical co-precipitation technique. The sample with x = 0.5 showed a saturation magnetization of 8.2 μ B which is the highest reported for any ferrite. Coupled to this excellent magnetic property, this ferrite has shown a negligible dielectric loss tangent over a large frequency window from 100 Hz to 1 MHz. The high values of saturation magnetization have been attributed to the composite effect of large-scale cationic migration and surface spin disorder.

  19. Is Chemically Synthesized Graphene ‘Really’ a Unique Substrate for SERS and Fluorescence Quenching?

    PubMed Central

    Sil, Sanchita; Kuhar, Nikki; Acharya, Somnath; Umapathy, Siva

    2013-01-01

    We demonstrate observation of Raman signals of different analytes adsorbed on carbonaceous materials, such as, chemically reduced graphene, graphene oxide (GO), multi-walled carbon nanotube (MWCNT), graphite and activated carbon. The analytes selected for the study were Rhodamine 6G (R6G) (in resonant conditions), Rhodamine B (RB), Nile blue (NBA), Crystal Violet (CV) and acetaminophen (paracetamol). All the analytes except paracetamol absorb and fluoresce in the visible region. In this article we provide experimental evidence of the fact that observation of Raman signals of analytes on such carbonaceous materials are more due to resonance effect, suppression of fluorescence and efficient adsorption and that this property in not unique to graphene or nanotubes but prevalent for various type of carbon materials. PMID:24275718

  20. Green light radiation effects on free radicals inhibition in cellular and chemical systems.

    PubMed

    Comorosan, Sorin; Polosan, Silviu; Jipa, Silviu; Popescu, Irinel; Marton, George; Ionescu, Elena; Cristache, Ligia; Badila, Dumitru; Mitrica, Radu

    2011-01-10

    Free radicals generation is inhibited through green light (GL) irradiation in cellular systems and in chemical reactions. Standard melanocyte cultures were UV-irradiated and the induced cellular reactive oxygen species (ROS) were quantified by the fluorescence technique. The same cell cultures, previously protected by a 24h GL exposure, displayed a significantly lower ROS production. A simple chemical reaction is subsequently chosen, in which the production of free radicals is well defined. Paraffin wax and mineral oil were GL irradiated during thermal degradation and the oxidation products checked by chemiluminescence [CL] and Fourier transform infrared spectra [FT-IR]. The same clear inhibition of the radical oxidation of alkanes is recorded. A quantum chemistry modeling of these results is performed and a mechanism involving a new type of Rydberg macromolecular systems with implications for biology and medicine is suggested. PMID:20934350

  1. Chain Assemblies from Nanoparticles Synthesized by Atmospheric Pressure Plasma Enhanced Chemical Vapor Deposition: The Computational View.

    PubMed

    Mishin, Maxim V; Zamotin, Kirill Y; Protopopova, Vera S; Alexandrov, Sergey E

    2015-12-01

    This article refers to the computational study of nanoparticle self-organization on the solid-state substrate surface with consideration of the experimental results, when nanoparticles were synthesised during atmospheric pressure plasma enhanced chemical vapor deposition (AP-PECVD). The experimental study of silicon dioxide nanoparticle synthesis by AP-PECVD demonstrated that all deposit volume consists of tangled chains of nanoparticles. In certain cases, micron-sized fractals are formed from tangled chains due to deposit rearrangement. This work is focused on the study of tangled chain formation only. In order to reveal their formation mechanism, a physico-mathematical model was developed. The suggested model was based on the motion equation solution for charged and neutral nanoparticles in the potential fields with the use of the empirical interaction potentials. In addition, the computational simulation was carried out based on the suggested model. As a result, the influence of such experimental parameters as deposition duration, particle charge, gas flow velocity, and angle of gas flow was found. It was demonstrated that electrical charges carried by nanoparticles from the discharge area are not responsible for the formation of tangled chains from nanoparticles, whereas nanoparticle kinetic energy plays a crucial role in deposit morphology and density. The computational results were consistent with experimental results. PMID:26682441

  2. Spark plasma sintering of tungsten-yttrium oxide composites from chemically synthesized nanopowders and microstructural characterization

    NASA Astrophysics Data System (ADS)

    Yar, M. A.; Wahlberg, Sverker; Bergqvist, Hans; Salem, H. G.; Johnsson, Mats; Muhammed, Mamoun

    2011-05-01

    Nano-crystalline W-1%Y 2O 3 (wt.%) powder was produced by a modified solution chemical reaction of ammonium paratungstate (APT) and yttrium nitrate. The precursor powder was found to consist of particles of bimodal morphology i.e. large APT-like particles up to 20 μm and rectangular yttrium containing ultrafine plates. After thermal processing tungsten crystals were evolved from W-O-Y plate like particles. spark plasma sintering (SPS) was used to consolidate the powder at 1100 and 1200 °C for different holding times in order to optimize the sintering conditions to yield high density but with reduced grain growth. Dispersion of yttrium oxide enhanced the sinterability of W powder with respect to lanthanum oxide. W-1%Y 2O 3 composites with sub-micron grain size showed improved density and mechanical properties as compared to W-La 2O 3 composites. Sample sintered in two steps showed improved density, due to longer holding time at lower temperature (900 °C) and less grain growth due to shorter holding time at higher temperature i.e. 1 min at 1100 °C.

  3. Coal gasification: Direct applications and syntheses of chemicals and fuels: A research needs assessment

    SciTech Connect

    Penner, S.S.; Alpert, S.B.; Beer, J.M.; Denn, M.; Haag, W.; Magee, R.; Reichl, E.; Rubin, E.S.; Solomon, P.R.; Wender, I.

    1987-06-01

    The DOE Working Group for an Assessment of Coal-Gasification Research Needs (COGARN - coal gasification advanced research needs) has reviewed and evaluated US programs dealing with coal gasification for a variety of applications. Cost evaluations and environmental-impact assessments formed important components of the deliberations. We have examined in some depth each of the following technologies: coal gasification for electricity generation in combined-cycle systems, coal gasification for the production of synthetic natural gas, coal gasifiers for direct electricity generation in fuel cells, and coal gasification for the production of synthesis gas as a first step in the manufacture of a wide variety of chemicals and fuels. Both catalytic and non-catalytic conversion processes were considered. In addition, we have constructed an orderly, long-range research agenda on coal science, pyrolysis, and partial combustion in order to support applied research and development relating to coal gasification over the long term. The COGARN studies were performed in order to provide an independent assessment of research needs in fuel utilization that involves coal gasification as the dominant or an important component. The findings and research recommendations of COGARN are summarized in this publication.

  4. Topological insulator Bi2Te3 films synthesized by metal organic chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Cao, Helin; Venkatasubramanian, Rama; Liu, Chang; Pierce, Jonathan; Yang, Haoran; Zahid Hasan, M.; Wu, Yue; Chen, Yong P.

    2012-10-01

    Topological insulator (TI) materials such as Bi2Te3 and Bi2Se3 have attracted strong recent interests. Large scale, high quality TI thin films are important for developing TI-based device applications. In this work, structural and electronic properties of Bi2Te3 thin films deposited by metal organic chemical vapor deposition (MOCVD) on GaAs (001) substrates were characterized via x-ray diffraction (XRD), Raman spectroscopy, angle-resolved photoemission spectroscopy (ARPES), and electronic transport measurements. The characteristic topological surface states with a single Dirac cone have been clearly revealed in the electronic band structure measured by ARPES, confirming the TI nature of the MOCVD Bi2Te3 films. Resistivity and Hall effect measurements have demonstrated relatively high bulk carrier mobility of ˜350 cm2/Vs at 300 K and ˜7400 cm2/Vs at 15 K. We have also measured the Seebeck coefficient of the films. Our demonstration of high quality topological insulator films grown by a simple and scalable method is of interests for both fundamental research and practical applications of thermoelectric and TI materials.

  5. It may be possible to construct a Chemical Synthesizing Computer based on Capillary Action

    NASA Astrophysics Data System (ADS)

    Kriske, Richard

    2013-03-01

    This author had previously proposed that Capillary Action has a Quantum Mechanical Model. This model can be easily constructed by noting that when a photon of the heat wavelength evaporates one molecule of water at the top of a capillary column, a ``hole'' is transmitted from the top of the column to the roots and into the water reservoir sustaining the capillary tube. This ``hole'' is a true hole (a true particle) in that it is transmitted as a quantized unit through the capillary tube. The mathematics of this process are the same as used in Quantum Field Theory, with the capillary acting as a perfect spring (like the spring used on a ``stack'' of dishes). When the external field using a force to pull the water molecule off the stack, an equal and opposite spring force (which is quantized), is transmitted down the column to the reservoir. When the water is not pure, this author proposes that each of the elements in the unpure water act linearly, each with its own quantized spring constant that does not interact with the other quantized spring constants, so it is possible to pull a single electron off the top of the water stack, yet the water in the stack is undisturbed (the reservoir is disturbed). Likewise it is possible to pull a sugar molecule off and balance chemical equations.

  6. Magnetic properties of Ni nanoparticles embedded in silica matrix (KIT-6) synthesized via novel chemical route

    SciTech Connect

    Dalavi, Shankar B.; Panda, Rabi N.; Raja, M. Manivel

    2015-06-24

    Thermally stable Ni nanoparticles have been embedded in mesoporous silica matrix (KIT-6) via novel chemical reduction method by using superhydride as reducing agent. X-ray diffraction (XRD) study confirms that pure and embedded Ni nanoparticles crystallize in face centered cubic (fcc) structure. Crystallite sizes of pure Ni, 4 wt% and 8 wt% Ni in silica were estimated to be 6.0 nm, 10.4 nm and 10.5 nm, respectively. Morphology and dispersion of Ni in silica matrix were studied by scanning electron microscopy (SEM). Magnetic study shows enhancement of magnetic moments of Ni nanoparticles embedded in silica matrix compared with that of pure Ni. The result has been interpreted on the basis of size reduction and magnetic exchange effects. Saturation magnetization values for pure Ni, 4 wt% and 8 wt% Ni in silica were found to be 15.77 emu/g, 5.08 emu/g and 2.00 emu/g whereas coercivity values were 33.72 Oe, 92.47 Oe and 64.70 Oe, respectively. We anticipate that the observed magnetic properties may find application as soft magnetic materials.

  7. Crystalline and transport properties of Ga2Te3 synthesized by metalorganic chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Su, Peng-Yu; Banerjee, Sneha; Dahal, Rajendra; Bhat, Ishwara B.

    2016-01-01

    Ga2Te3 films have been grown on GaAs(100) and (111) substrates using metalorganic chemical vapor deposition (MOCVD) at temperatures ranging from 350°C to 450°C. Very uniform films were grown at lower temperatures of 350°C on GaAs(100) substrates. As the temperature increased the roughness of the films increased, with many hillocks observed on films deposited at 450°C. The Ga2Te3 films grown on GaAs(100) were determined to be single crystal by XRD characterization. On the other hand, XRD scans confirmed crystal twinning in the Ga2Te3 films grown on GaAs(111) and the surface morphology also indicated the presence of twin grains. The films were determined to be n-type by hot-point probe testing. The carrier concentration could not be measured precisely as after photoexcitation, Ga2Te3 exhibited the persistent photoconductivity (PPC) effect. [Figure not available: see fulltext.

  8. Resistive Switching of Individual, Chemically Synthesized TiO2 Nanoparticles.

    PubMed

    Schmidt, Dirk Oliver; Hoffmann-Eifert, Susanne; Zhang, Hehe; La Torre, Camilla; Besmehn, Astrid; Noyong, Michael; Waser, Rainer; Simon, Ulrich

    2015-12-22

    Resistively switching devices are considered promising for next-generation nonvolatile random-access memories. Today, such memories are fabricated by means of "top-down approaches" applying thin films sandwiched between nanoscaled electrodes. In contrast, this work presents a "bottom-up approach" disclosing for the first time the resistive switching (RS) of individual TiO2 nanoparticles (NPs). The NPs, which have sizes of 80 and 350 nm, respectively, are obtained by wet chemical synthesis and thermally treated under oxidizing or vacuum conditions for crystallization, respectively. These NPs are deposited on a Pt/Ir bottom electrode and individual NPs are electrically characterized by means of a nanomanipulator system in situ, in a scanning electron microscope. While amorphous NPs and calcined NPs reveal no switching hysteresis, a very interesting behavior is found for the vacuum-annealed, crystalline TiO(2-x) NPs. These NPs reveal forming-free RS behavior, dominantly complementary switching (CS) and, to a small degree, bipolar switching (BS) characteristics. In contrast, similarly vacuum-annealed TiO2 thin films grown by atomic layer deposition show standard BS behavior under the same conditions. The interesting CS behavior of the TiO(2-x) NPs is attributed to the formation of a core-shell-like structure by re-oxidation of the reduced NPs as a unique feature. PMID:26540646

  9. Nanostructured zinc oxide films synthesized by successive chemical solution deposition for gas sensor applications

    SciTech Connect

    Lupan, O. Chow, L.; Shishiyanu, S.; Monaico, E.; Shishiyanu, T.; Sontea, V.; Roldan Cuenya, B.; Naitabdi, A.; Park, S.; Schulte, A.

    2009-01-08

    Nanostructured ZnO thin films have been deposited using a successive chemical solution deposition method. The structural, morphological, electrical and sensing properties of the films were studied for different concentrations of Al-dopant and were analyzed as a function of rapid photothermal processing temperatures. The films were investigated by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron and micro-Raman spectroscopy. Electrical and gas sensitivity measurements were conducted as well. The average grain size is 240 and 224 A for undoped ZnO and Al-doped ZnO films, respectively. We demonstrate that rapid photothermal processing is an efficient method for improving the quality of nanostructured ZnO films. Nanostructured ZnO films doped with Al showed a higher sensitivity to carbon dioxide than undoped ZnO films. The correlations between material compositions, microstructures of the films and the properties of the gas sensors are discussed.

  10. Promising wet chemical strategies to synthesize Cu nanowires for emerging electronic applications

    NASA Astrophysics Data System (ADS)

    Ravi Kumar, D. V.; Woo, Kyoohee; Moon, Jooho

    2015-10-01

    Copper nanowires (Cu NWs) are of particular interest for application as transparent and flexible conducting electrodes in `see-through' and/or `deformable' future electronics due to their excellent electrical, optical, and mechanical properties. It is necessary to develop reliable and facile methods to produce well-defined Cu NWs prior to their full exploitation. Among the wide variety of methods available to generate Cu NWs, solution-based synthesis routes are considered to be a promising strategy because of several advantages including fewer constraints on the selection of precursors, the solvent and reaction conditions, and the feasibility of large-scale low-cost production. Here, we provide a thorough review of various recently developed synthetic methodologies to obtain Cu NWs, with particular emphasis on wet chemical synthesis approaches including a hydrothermal route, reduction of metal precursors, and catalytic synthesis. The emerging applications of Cu NWs including transparent electrodes and flexible/stretchable electronics are also discussed, followed by brief comments on the remaining challenges and future research perspectives.

  11. Structural and photoluminescence properties of Eu(3+) doped α-Ag2WO4 synthesized by the green coprecipitation methodology.

    PubMed

    Pinatti, Ivo M; Nogueira, Içamira C; Pereira, Wyllamanney S; Pereira, Paula F S; Gonçalves, Rosana F; Varela, José A; Longo, Elson; Rosa, Ieda L V

    2015-10-28

    Europium doped silver tungstates α-Ag2-3xEuxWO4 (x = 0, 0.0025, 0.005, 0.0075 and 0.01 mol) were synthesized by the coprecipitation method at 90 °C for 30 minutes. These crystals were structurally characterized by means of X-ray diffraction (XRD), Rietveld refinement, and micro-Raman (MR) and Fourier transformed infrared (FT-IR) spectroscopies. Field emission scanning electron microscopy (FE-SEM) images were employed to observe the shape of the crystals. The optical properties were investigated by ultraviolet-visible (UV-vis) absorption and photoluminescence (PL) measurements. The XRD pattern indicated structural organization at a long range for all undoped and Eu-doped samples, while MR and FT-IR revealed that the presence of the Eu(3+) ions favors the structural organization at a short range. The Rietveld refinement showed that all the crystals are monophasic with an orthorhombic structure and the Pn2[combining macron]n space group. The refined lattice parameters and atomic positions were employed to model the WO6 and AgOn (n = 2, 4, 6 and 7) polyhedra in the unit cell. FE-SEM analysis revealed nanorod-like microcrystals with growth of metallic silver on the surface. Further, the UV-vis absorption spectra indicated the existence of intermediary energy levels within the band gap. PL spectra showed a broad band related to the [WO6] group and characteristic narrow peaks due to the f-f transitions of Eu(3+) as a result of efficient energy transfer from the matrix. Also, the emission line shape transitions from (5)D0 to (7)FJ (J = 0-4) levels of the Eu(3+) were noticed. Among the samples, the most intense photoluminescence results were observed for the α-Ag2-3xEuxWO4 (x = 0.0075) sample. Lifetime decays support that the Eu(3+) ions occupy at least two crystallographic sites. CIE coordinates confirmed the colors of the emission spectra which classify this material as a potential phosphor in the visible range. PMID:26394903

  12. Polyvinyl polypyrrolidone attenuates genotoxicity of silver nanoparticles synthesized via green route, tested in Lathyrus sativus L. root bioassay.

    PubMed

    Panda, Kamal K; Achary, V Mohan M; Phaomie, Ganngam; Sahu, Hrushi K; Parinandi, Narasimham L; Panda, Brahma B

    2016-08-01

    The silver nanoparticles (AgNPs) were synthesized extracellularly from silver nitrate (AgNO3) using kernel extract from ripe mango Mengifera indica L. under four different reaction conditions of the synthesis media such as the (i) absence of the reducing agent, trisodium citrate (AgNPI), (ii) presence of the reducing agent (AgNPII), (iii) presence of the cleansing agent, polyvinyl polypyrrolidone, PVPP (AgNPIII), and (iv) presence of the capping agent, polyvinyl pyrrolidone, PVP (AgNPIV). The synthesis of the AgNPs was monitored by UV-vis spectrophotometry. The AgNPs were characterised by the energy-dispersive X-ray spectroscopy, transmission electron microscopy, X-ray diffraction, and small-angle X-ray scattering. Functional groups on the AgNPs were established by the Fourier transform infrared spectroscopy. The AgNPs (AgNPI, AgNPII, AgNPIII and AgNPIV) were spherical in shape with the diameters and size distribution-widths of 14.0±5.4, 19.2±6.6, 18.8±6.6 and 44.6±13.2nm, respectively. Genotoxicity of the AgNPs at concentrations ranging from 1 to 100mgL(-1) was determined by the Lathyrus sativus L. root bioassay and several endpoint assays including the generation of reactive oxygen species and cell death, lipid peroxidation, mitotic index, chromosome aberrations (CA), micronucleus formation (MN), and DNA damage as determined by the Comet assay. The dose-dependent induction of genotoxicity of the silver ion (Ag(+)) and AgNPs was in the order Ag(+)>AgNPII>AgNPI>AgNPIV>AgNPIII that corresponded with their relative potencies of induction of DNA damage and oxidative stress. Furthermore, the findings underscored the CA and MN endpoint-based genotoxicity assay which demonstrated the genotoxicity of AgNPs at concentrations (≤10mgL(-1)) lower than that (≥10mgL(-1)) tested in the Comet assay. This study demonstrated the protective action of PVPP against the genotoxicity of AgNPIII which was independent of the size of the AgNPs in the L. sativus L. root bioassay

  13. Toward a New U.S. Chemicals Policy: Rebuilding the Foundation to Advance New Science, Green Chemistry, and Environmental Health

    PubMed Central

    Wilson, Michael P.; Schwarzman, Megan R.

    2009-01-01

    Objective We describe fundamental weaknesses in U.S. chemicals policy, present principles of chemicals policy reform, and articulate interdisciplinary research questions that should be addressed. With global chemical production projected to double over the next 24 years, federal policies that shape the priorities of the U.S. chemical enterprise will be a cornerstone of sustainability. To date, these policies have largely failed to adequately protect public health or the environment or motivate investment in or scientific exploration of cleaner chemical technologies, known collectively as green chemistry. On this trajectory, the United States will face growing health, environmental, and economic problems related to chemical exposures and pollution. Conclusions Existing policies have produced a U.S. chemicals market in which the safety of chemicals for human health and the environment is undervalued relative to chemical function, price, and performance. This market barrier to green chemistry is primarily a consequence of weaknesses in the Toxic Substances Control Act. These weaknesses have produced a chemical data gap, because producers are not required to investigate and disclose sufficient information on chemicals’ hazard traits to government, businesses that use chemicals, or the public; a safety gap, because government lacks the legal tools it needs to efficiently identify, prioritize, and take action to mitigate the potential health and environmental effects of hazardous chemicals; and a technology gap, because industry and government have invested only marginally in green chemistry research, development, and education. Policy reforms that close the three gaps—creating transparency and accountability in the market—are crucial for improving public and environmental health and reducing the barriers to green chemistry. The European Union’s REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) regulation has opened an opportunity for

  14. Investigation on growth behavior of CNTs synthesized by atmospheric pressure plasma enhanced chemical vapor deposition system on Fe catalyzed substrate.

    PubMed

    Choi, Bum Ho; Kim, Won Jae; Kim, Young Baek; Lee, Jong Ho; Park, Jong Woon; Kim, Woo Sam; Shin, Dong Chan

    2008-10-01

    We have studied growth behavior of carbon nanotubes (CNTs) on iron (Fe) catalyzed substrate using newly developed atmospheric pressure plasma enhanced chemical vapor deposition (AP-PECVD) system. To investigate the improved growth performance with simple equipment and process on large scale, a new AP-PECVD system containing different concept on downstream gas was designed and manufactured. As a catalyst, either sputtered or evaporated Fe thin film on SiO2/Si substrate was used and acetylene gas was used as a carbon source. We observed growth behavior of CNTs such as height, rate and density were strongly affected by plasma power. The maximum height of 427 microm and 267 microm was synthesized under RF plasma power of 30 W for 30 min and 40 W for 3 min, respectively. The growth rate dramatically increased to 6.27 times as plasma power increased from 30 to 40 W which opens the possibility the mass production of CNTs. By SEM and TEM observation, it was verified the grown CNTs was consists of mixture of single-wall and multi-wall CNTs. The graphitization ratio was measured to be 0.93, indicating that the graphitized CNTs forest was formed and relatively high purity of CNTs was synthesized, being useful for nano-composite materials to reinforce the strength. From our experiments, we can observe that the height and growth rate of CNTs is strong function of plasma power. PMID:19198378

  15. Physical and electrochemical properties of synthesized carbon nanotubes [CNTs] on a metal substrate by thermal chemical vapor deposition

    PubMed Central

    2012-01-01

    Multi-walled carbon nanotubes were synthesized on a Ni/Au/Ti substrate using a thermal chemical vapor deposition process. A Ni layer was used as a catalyst, and an Au layer was applied as a barrier in order to prevent diffusion between Ni and Ti within the substrate during the growth of carbon nanotubes. The results showed that vertically aligned multi-walled carbon nanotubes could be uniformly grown on the Ti substrate (i.e., metal substrate), thus indicating that the Au buffer layer effectively prevented interdiffusion of the catalyst and metal substrate. Synthesized carbon nanotubes on the Ti substrate have the diameter of about 80 to 120 nm and the length of about 5 to 10 μm. The Ti substrate, with carbon nanotubes, was prepared as an electrode for a lithium rechargeable battery, and its electrochemical properties were investigated. In a Li/CNT cell with carbon nanotubes on a 60-nm Au buffer layer, the first discharge capacity and discharge capacity after the 50th cycle were 210 and 80 μAh/cm2, respectively. PMID:22221861

  16. Dielectric properties and electrical conductivity of MgO synthesized by chemical precipitation and sol-gel method

    NASA Astrophysics Data System (ADS)

    Mbarki, Rabeh; Hichem Hamzaoui, Ahmed; Mnif, Adel

    2015-01-01

    MgO Powders were synthesized via simple chemical precipitation (SPC) and sol-gel process (SG). The electrical behavior of these powders was determined by complex impedance spectroscopy using an alternative current conductivity at various temperatures and frequencies. For MgO elaborated by SG, the activation energy is 1.49 eV while MgO prepared by SPC, this energy is equal to 0.39 and 4.13 eV. The structural properties of MgO powders were analyzed by X-ray diffraction and FT-IR spectroscopy. The results show that the cristallites size was 28.4 nm for MgO SPC and 42.5 nm for MgO SG. Others methods such DTA, TGA, BET and SEM were used to characterized MgO materials.

  17. Accelerating the degradation of green plant waste with chemical decomposition agents.

    PubMed

    Kejun, Sun; Juntao, Zhang; Ying, Chen; Zongwen, Liao; Lin, Ruan; Cong, Liu

    2011-10-01

    Degradation of green plant waste is often difficult, and excess maturity times are typically required. In this study, we used lignin, cellulose and hemicellulose assays; scanning electron microscopy; infrared spectrum analysis and X-ray diffraction analysis to investigate the effects of chemical decomposition agents on the lignocellulose content of green plant waste, its structure and major functional groups and the mechanism of accelerated degradation. Our results showed that adding chemical decomposition agents to Ficus microcarpa var. pusillifolia sawdust reduced the contents of lignin by 0.53%-11.48% and the contents of cellulose by 2.86%-7.71%, and increased the contents of hemicellulose by 2.92%-33.63% after 24 h. With increasing quantities of alkaline residue and sodium lignosulphonate, the lignin content decreased. Scanning electron microscopy showed that, after F. microcarpa var. pusillifolia sawdust was treated with chemical decomposition agents, lignocellulose tube wall thickness increased significantlyIncreases of 29.41%, 3.53% and 34.71% were observed after treatment with NaOH, alkaline residue and sodium lignosulphonate, respectively. Infrared spectroscopy showed that CO and aromatic skeleton stretching absorption peaks were weakened and the C-H vibrational absorption peak from out-of-plane in positions 2 and 6 (S units) (890-900 cm(-1)) was strengthened after F. microcarpa var. pusillifolia sawdust was treated with chemical decomposition agents, indicating a reduction in lignin content. Several absorption peaks [i.e., C-H deformations (asymmetry in methyl groups, -CH(3)- and -CH(2)-) (1450-1460 cm(-1)); Aliphatic C-H stretching in methyl and phenol OH (1370-1380 cm(-1)); CO stretching (cellulose and hemicellulose) (1040-1060 cm(-1))] that indicate the presence of a chemical bond between lignin and cellulose was reduced, indicating that the chemical bond between lignin and cellulose had been partially broken. X-ray diffraction analysis showed that Na

  18. Comparison of structural and luminescence properties of Dy{sub 2}O{sub 3} nanopowders synthesized by co-precipitation and green combustion routes

    SciTech Connect

    Chandrasekhar, M.; Nagabhushana, H.; Sudheerkumar, K.H.; Dhananjaya, N.; Sharma, S.C.; Kavyashree, D.; Shivakumara, C.; Nagabhushana, B.M.

    2014-07-01

    Highlights: • Dy{sub 2}O{sub 3} nanopowders were prepared by co-precipitation and eco-friendly green combustion route using plant latex. • Both the products show excellent chromaticity coordinates in the white region, which were quite useful for white LED’s. • Thermoluminescence response of the Dy{sub 2}O{sub 3} product prepared by green synthesis was higher when compared to co-precipitation route. • Structural parameters of Dy{sub 2}O{sub 3} were estimated using Rietveld refinement. • The development of nanosize materials using eco-friendly resources was an attractive non-hazardous chemical route. - Abstract: Dysprosium oxide (Dy{sub 2}O{sub 3}) nanopowders were prepared by co-precipitation (CP) and eco-friendly green combustion (GC) routes. SEM micrographs prepared by CP route show smooth rods with various lengths and diameters while, GC route show porous, agglomerated particles. The results were further confirmed by TEM. Thermoluminescence (TL) responses of the nanopowder prepared by both the routes were studied using γ-rays. A well resolved glow peak at 353 °C along with less intense peak at 183 °C was observed in GC route while, in CP a single glow peak at 364 °C was observed. The kinetic parameters were estimated using Chen’s glow peak route. Photoluminescence (PL) of Dy{sub 2}O{sub 3} shows peaks at 481, 577, 666 and 756 nm which were attributed to Dy{sup 3+} transitions of {sup 4}F{sub 9/2}⟶{sup 6}H{sub 15/2}, {sup 6}H{sub 13/2}, {sup 6}H{sub 11/2} and {sup 6}H{sub 9/2}, respectively. Color co-ordinate values were located in the white region as a result the product may be useful for the fabrication of WLED’S.

  19. ZnS nanocrystals and nanoflowers synthesized by a green chemistry approach: rare excitonic photoluminescence achieved by the tunable molar ratio of precursors.

    PubMed

    Xiao, Ningru; Dai, Quanqin; Wang, Yingnan; Ning, Jiajia; Liu, Bingbing; Zou, Guangtian; Zou, Bo

    2012-04-15

    In the present work, we demonstrated a simple and green synthesis route for shape-controlled ZnS nanocrystals, where only environmentally benign chemicals, namely sulfur, zinc oxide and olive oil, were employed. By controlling the experimental conditions, we were able to tune the band edge and trap state photoluminescences of ZnS nanocrystals and obtain pure excitonic photoluminescence that was rarely observed in literature. The trap state emission was derived from sulfur vacancies and would be eliminated when an excess of sulfur was used during the synthesis. Additionally, the morphology of ZnS nanocrystals could be tuned to appear like flowers, where the formation mechanism was systematically discussed. PMID:22138176

  20. The preparation of site-specifically modified riboswitch domains as an example for enzymatic ligation of chemically synthesized RNA fragments.

    PubMed

    Lang, Kathrin; Micura, Ronald

    2008-01-01

    This protocol describes an efficient method for the preparation of riboswitch domains comprising up to approximately 200 nt containing site-specific nucleoside modifications. The strategy is based on enzymatic ligation of chemically synthesized RNA fragments. The design of ligation sites strictly follows the criterion that all fragments comprise less than approximately 50 nt. This allows the researcher to rely on custom synthesis services and to utilize the large pool of commercially available, functionalized nucleoside phosphoramidites for solid-phase RNA synthesis. Importantly, this design renders utmost flexibility to position a chemical modification (e.g., a fluorescence label) within the RNA. Selection of the appropriate ligation type (using T4 RNA or T4 DNA ligase) is subordinate to the criteria above and is detailed in the protocol. The whole concept is demonstrated for 2-aminopurine containing thiamine pyrophosphate responsive riboswitch domains that are applied in fluorescence spectroscopic folding studies. Labeled samples in 5-35 nmol quantities are obtained within 3-4 d, not including the time for fragment synthesis. PMID:18772873

  1. Chemical characterization of Lippia alba essential oil: an alternative to control green molds.

    PubMed

    Glamočlija, Jasmina; Soković, Marina; Tešević, Vele; Linde, Giani Andrea; Colauto, Nelson Barros

    2011-10-01

    The essential oil of Lippia alba is reported as an antifungal against human pathogenic microorganisms but few articles report its use as an alternative to synthetic fungicides on green mould control. The objective of this study was to determine chemical characteristics of L. alba essential oil and its antifungal activity against green molds as an alternative to synthetic fungicides. Essential oil was extracted by Clevenger hydrodistillation, characterized by GC-MS analysis, and the structure of the main compounds confirmed by (1)H and (13)C-NMR spectroscopy. Microdilution assays evaluated the essential oil minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC). Commercial fungicides Ketoconazole and Bifonazole were used as control. Essential oil yield is of 0.15% and the major components are neral (33.32%) and geranial (50.94%). The L. alba essential oil has MIC of 0.300-1.250 mg/mL and MFC of 0.600-1.250 mg/mL. Ketoconazole and Bifonazole show MIC ranging from 0.025-0.500 to 0.100-0.200 mg/mL, and MFC ranging from 0.250-0.100 to 0.200-0.250 mg/mL, respectively. L. alba essential oil is classified as citral type and the results indicate that it is a potential alternative to synthetic fungicides. PMID:24031788

  2. Study of green Sicilian table olive fermentations through microbiological, chemical and sensory analyses.

    PubMed

    Aponte, Maria; Ventorino, Valeria; Blaiotta, Giuseppe; Volpe, Giorgio; Farina, Vittorio; Avellone, Giuseppe; Lanza, Carmela Maria; Moschetti, Giancarlo

    2010-02-01

    The production of five different green table olive cultivars was studied by a combined strategy consisting of chemical, microbiological and sensory analyses. Cultivable microflora of samples collected during processing was monitored by plate counts on seven synthetic culture media. In all samples Enterobacteriaceae, Pseudomonaceae, staphylococci, lactic acid bacteria and spore-forming bacteria were undetectable. Yeasts and moulds were countable from the day 42 (2 log CFU/ml) till the end of fermentation (6 log CFU/ml). The use of three different approaches for microorganism detection, including a culture-independent methodology, revealed the presence of barely three yeast species during the entire fermentation period: Candida parapsilosis, Pichia guilliermondii and Pichia kluyveri. Biochemical features of technological interest were evaluated for 94 strains in order to investigate their potential role in fermentation of green Sicilian table olives. Olive drupes sampled at picking and periodically during fermentation were also carpologically analyzed, revealing that all the cultivars were suitable for table olive fermentation process. After 120 days of fermentation all products met acceptable commercial standards, although GC-MS analysis evidenced several differences among varieties in terms of aroma components. Results from sensory evaluation led to the conclusion that a revision of technological procedures may improve the final quality of product. PMID:19913708

  3. Chemical characterization of Lippia alba essential oil: an alternative to control green molds

    PubMed Central

    Glamočlija, Jasmina; Soković, Marina; Tešević, Vele; Linde, Giani Andrea; Colauto, Nelson Barros

    2011-01-01

    The essential oil of Lippia alba is reported as an antifungal against human pathogenic microorganisms but few articles report its use as an alternative to synthetic fungicides on green mould control. The objective of this study was to determine chemical characteristics of L. alba essential oil and its antifungal activity against green molds as an alternative to synthetic fungicides. Essential oil was extracted by Clevenger hydrodistillation, characterized by GC-MS analysis, and the structure of the main compounds confirmed by 1H and 13C-NMR spectroscopy. Microdilution assays evaluated the essential oil minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC). Commercial fungicides Ketoconazole and Bifonazole were used as control. Essential oil yield is of 0.15% and the major components are neral (33.32%) and geranial (50.94%). The L. alba essential oil has MIC of 0.300–1.250 mg/mL and MFC of 0.600–1.250 mg/mL. Ketoconazole and Bifonazole show MIC ranging from 0.025–0.500 to 0.100–0.200 mg/mL, and MFC ranging from 0.250–0.100 to 0.200–0.250 mg/mL, respectively. L. alba essential oil is classified as citral type and the results indicate that it is a potential alternative to synthetic fungicides. PMID:24031788

  4. Method for recovering sodium chemicals from green liquor and flue gases

    SciTech Connect

    Rimpi, P.

    1984-09-11

    The invention relates to a method for recovering sodium chemicals from green liquor by precarbonating green liquor by means of flue gases, by bringing a precarbonated solution into contact with a sodium bicarbonate solution and by stripping hydrogen sulphide from the so obtained reaction mixture by means of steam, for producing hydrogen sulphide gas and a sodium carbonate solution, which sodium carbonate solution is so pure, in relation to sodium sulphide that it can directly be led into the washing of the flue gases and into a carbonation stage, for producing the sodium bicarbonate solution. In order to save steam and sodium carbonate all precarbonated solution is not treated to the sodium sulphide free solution, which is required by a scrubber, but a part is discharged at higher sodium sulphide content by dividing the stripping into two stages which take place one above the other in the same tower, whereby a part of a solution obtained from the first stripping stage is led directly into the second stripping stage and the steams containing hydrogen sulphide, obtained from the second stripping stage are led directly into the first stripping stage.

  5. Soft ionization chemical analysis of secondary organic aerosol from green leaf volatiles emitted by turf grass.

    PubMed

    Jain, Shashank; Zahardis, James; Petrucci, Giuseppe A

    2014-05-01

    Globally, biogenic volatile organic compound (BVOC) emissions contribute 90% of the overall VOC emissions. Green leaf volatiles (GLVs) are an important component of plant-derived BVOCs, including cis-3-hexenylacetate (CHA) and cis-3-hexen-1-ol (HXL), which are emitted by cut grass. In this study we describe secondary organic aerosol (SOA) formation from the ozonolysis of dominant GLVs, their mixtures and grass clippings. Near-infrared laser desorption/ionization aerosol mass spectrometry (NIR-LDI-AMS) was used for chemical analysis of the aerosol. The chemical profile of SOA generated from grass clippings was correlated with that from chemical standards of CHA and HXL. We found that SOA derived from HXL most closely approximated SOA from turf grass, in spite of the approximately 5× lower emission rate of HXL as compared to CHA. Ozonolysis of HXL results in formation of low volatility, higher molecular weight compounds, such as oligomers, and formation of ester-type linkages. This is in contrast to CHA, where the hydroperoxide channel is the dominant oxidation pathway, as oligomer formation is inhibited by the acetate functionality. PMID:24666343

  6. Protective effects of green tea on antioxidative biomarkers in chemical laboratory workers.

    PubMed

    Tavakol, Heidary Shayesteh; Akram, Ranjbar; Azam, Sayadi; Nahid, Zadkhosh

    2015-09-01

    Chemical materials are environmental contaminants, are extensively used in laboratories, and may cause various forms of health hazards in laboratory workers. Therefore, this toxicity most likely is a result of the oxidative metabolism of chemical to reactive products. As green tea (GT) possesses antioxidant effects, the objective of this study was to examine any amelioration oxidative stress in chemical laboratory workers drinking one cup (3 g/300 ml water) of freshly prepared tea once daily. Baseline characteristics including age, sex, smoking, fruit consumption, and duration of exposure were recorded via questionnaire to the subjects. Saliva level oxidative stress parameters such as total antioxidant capacity (TAC), glutathione peroxidase (GPx), catalase (CAT), and superoxide dismutase (SOD) were estimated before and after consumption of GT in these workers. Treatment of subjects with GT induced a significant reduction in saliva GPx activity (406.61 ± 22.07 vs. 238.96 ± 16.26 U/l p = 0.001) and induction in TAC (0.46 ± 0.029 μmol/ml vs. 0.56 ± 0.031, p = 0.016). No statistically significant alteration was found for saliva SOD (0.080 ± 0.0019 vs. 0.079 ± 0.0014, p > 0.05) and CAT (20.36 ± 0.69 vs. 19.78 ± 0.71, p > 0.05) after 28 days treatment by GT. These results demonstrate that drinking GT during chemical exposure can reduce several parameters indicative of oxidative stress. In conclusion, using GT as a dietary supplement can be a rational protocol to control source of hazards in chemical laboratory workers. PMID:23576111

  7. Photo-catalytic activity of Plasmonic Ag@AgCl nanoparticles (synthesized via a green route) for the effective degradation of Victoria Blue B from aqueous phase.

    PubMed

    Devi, Th Babita; Begum, Shamima; Ahmaruzzaman, M

    2016-07-01

    This study reports a green process for the fabrication of Ag@AgCl (silver@silver chloride) nanoparticles by using Aquilaria agallocha (AA) leaves juice without using any external reagents. The effect of various reaction parameters, such as reaction temperature, reaction time and concentration of Aquilaria agallocha leaves juice in the formation of nanoparticles have also been investigated. From the FTIR spectra of leaves juice and phytochemicals test, it was found that flavonoids present in the leaves are responsible for the reduction of Ag(+) ions to Ag(0) species and leads to the formation of Ag@AgCl NPs. The synthesized Ag@AgCl NPs were utilized for the removal of toxic and hazardous dyes, such as Victoria Blue B from aqueous phase. Approximately, 99.46% degradation of Victoria Blue B dye were observed with Ag@AgCl NPs. Furthermore, the photocatalytic activity of the Ag@AgCl nanoparticles was unchanged after 5cycles of operation. PMID:27152674

  8. The effects of whole green tea infusion on mouse urinary bladder chemical carcinogenesis

    PubMed Central

    Henriques, Andreia; Arantes-Rodrigues, Regina; I Faustino-Rocha, Ana; I Teixeira-Guedes, Catarina; Pinho-Oliveira, Jacinta; Talhada, Daniela; H Teixeira, José; Andrade, Andreia; Colaço, Bruno; N Paiva-Cardoso, Maria; J Pires, Maria; MVD Ferreira, Ana; M Nunes, Fernando; A Oliveira, Paula

    2014-01-01

    Objective(s): Green tea (GT) is one of the most popular beverages worldwide whose beneficial effects on health have been demonstrated. Recent studies suggest that GT may contribute to reduction of cancer risk and progression. The aim of this study was to evaluate the effects of whole GT on urinary bladder chemical carcinogenesis in male and female ICR mice. Materials and Methods: The GT characterization was performed using spectrophotometric methods. Urinary bladder lesions were induced using N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) by gavage during 10 weeks and whole GT (0.5%) was provided ad libitum during 20 weeks. Results: Animals from groups BBN+GT and BBN only developed preneoplastic lesions. Conclusion: We did not observe any effects by GT infusion administration on urinary bladder cancer development. PMID:24711900

  9. Unveiling the Nature of the "Green Pea" Galaxies: Oxygen and Nitrogen Chemical Abundances

    NASA Astrophysics Data System (ADS)

    Amorín, R. O.; Pérez-Montero, E.; Vílchez, J. M.

    2011-07-01

    We present recent results on the oxygen and nitrogen chemical abundances in the extremely compact, low-mass starburst galaxies at redshifts 0.1-0.3 usually referred to as "green pea" galaxies. We show that they are metal-poor galaxies (~1/5 solar) with lower oxygen abundances than star-forming galaxies of similar mass and N/O ratios unusually high for galaxies of the same metallicity. Recent, rapid, and massive inflows of cold gas, possibly coupled with enriched outflows from supernova winds, are used to explain the results. This is consistent with the known "pea" galaxy properties and suggest that these rare objects are experiencing a short and extreme phase in their evolution.

  10. A green chemical approach for synthesis of shape anisotropic gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Kalyan Kamal, S. S.; Vimala, J.; Sahoo, P. K.; Ghosal, P.; Ram, S.; Durai, L.

    2014-06-01

    A complete green chemical reaction between aurochloric acid and tea polyphenols resulted in the reduction of Au3+ → Au0. The reaction was carried out in a Teflon-coated bomb digestion vessel at 200 °C. It was observed that with increasing the reaction time from 1 to 5 h, the shape of the nanoparticles changed from spherical- to rod-like structures. The reaction was followed with the help of UV-vis spectrometer, which showed a single absorption peak at 548 nm for 1-h reaction product and two peaks for a 5-h reaction product at 533 and 745 nm corresponding to the transverse and longitudinal surface plasmon resonance bands. Microstructures obtained from transmission electron microscope revealed that the samples obtained after 1-h reaction are predominantly spherical in shape with an average size of 15 nm. Whereas samples obtained after 5 h of reaction exhibited rod-like structures with an average size of 45 nm.

  11. Investigation of non-linear optical properties of CdS/PS polymer nanocomposite synthesized by chemical route

    NASA Astrophysics Data System (ADS)

    Tripathi, S. K.; Kaur, Ramneek; Jyoti

    2015-10-01

    Cadmium Sulfide (CdS) nanoparticles play an important role in non-linear optoelectronic devices. CdS/Polystyrene(PS) nanocomposite has been prepared by chemical ex-situ route and characterized by X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet-visible (UV-vis) and Photoluminescence (PL) spectroscopy. XRD spectra of CdS/PS nanocomposite reveals the cubic phase of CdS nanoparticles with average crystallite size ~2.54 nm. The vibrational band corresponding to Cd-S bond has been observed at 406.57 cm-1 in FTIR spectra of CdS/PS nanocomposite along the typical styrene bonds. Quantum confinement effect in the CdS/PS nanocomposite has been confirmed from the UV-vis spectra. In PL emission spectra, in addition to band to band transition emission, the green and yellow bands have been observed due to the interstitial sulfur and cadmium defect states respectively. Z-scan technique has been utilized to study the non-linear optical properties of the CdS/PS nanocomposite. The value of non-linear absorption coefficient (β) and non-linear refractive index (n2) has been calculated. The large value of third order non-linear susceptibility is due to the quantum confinement effect plus the thermal lensing effect produced across the sample.

  12. The reaction mechanism of formation of chemically synthesized Nd{sub 2}Fe{sub 14}B hard magnetic nanoparticles

    SciTech Connect

    Deheri, P.K.; Shukla, S.; Ramanujan, R.V.

    2012-02-15

    Nd{sub 2}Fe{sub 14}B based magnetic materials exhibit excellent magnetic properties and are widely used in many engineering applications. However, chemical synthesis of this compound is challenging. In this work, the formation mechanism of chemically synthesized Nd{sub 2}Fe{sub 14}B magnetic nanoparticles was studied. Nd, Fe and B precursors were converted to Nd-Fe-B oxide by the sol-gel method, reduction of these oxides by CaH{sub 2} resulted in Nd{sub 2}Fe{sub 14}B nanoparticles. Nd{sub 2}Fe{sub 14}B phase formation resulted from two competing reactions: (a) Nd{sub 2}Fe{sub 14}B phase formation by direct combination of NdH{sub 2}, Fe and B, (b) Nd{sub 2}Fe{sub 17} phase formation from NdH{sub 2} and Fe, followed by Nd{sub 2}Fe{sub 14}B phase formation by the reaction of Nd{sub 2}Fe{sub 17} and B. Addition of boron to Nd-Fe-B oxide during reduction resulted in improved magnetic properties. The activation energy for Nd{sub 2}Fe{sub 14}B phase formation was found to be 365 kJ mol{sup -1}. The optimum heat treatment temperature and time for Nd{sub 2}Fe{sub 14}B phase formation were found to be 800 Degree-Sign C and 90 min, respectively. - Graphical abstract: The kinetics, reaction mechanism and morphology of Nd{sub 2}Fe{sub 14}B magnetic nanoparticles synthesized by sol-gel followed by reduction-diffusion at 800 Degree-Sign C. Highlights: Black-Right-Pointing-Pointer The formation mechanism of Nd{sub 2}Fe{sub 14}B magnetic nanoparticles was studied. Black-Right-Pointing-Pointer Nd{sub 2}Fe{sub 14}B phase formation occurs by two parallel competing reactions. Black-Right-Pointing-Pointer Reaction of NdH{sub 2}, Fe and B resulted in Nd{sub 2}Fe{sub 14}B phase formation. Black-Right-Pointing-Pointer Nd{sub 2}Fe{sub 14}B phase can also be formed by the reaction of Nd{sub 2}Fe{sub 17} and B. Black-Right-Pointing-Pointer Maximum wt% of Nd{sub 2}Fe{sub 14}B phase was obtained at 800 Degree-Sign C and 90 min annealing.

  13. A novel green chemical route for synthesis of silver nanoparticles using camellia sinensis.

    PubMed

    Kamal, Sarika Srinivas Kalyan; Sahoo, Prasanta Kumar; Vimala, Johnson; Premkumar, Manda; Ram, Shanker; Durai, Loganathan

    2010-12-01

    The thrust to develop environmental friendly procedures for production of Nanoparticles arises from the very fact that current nanotechnology research uses a lot of chemicals, which are potential threat to both environment and public health. Tea (Camellia Sinensis) with its rich source of polyphenolic compounds has been exploited for the reduction and capping of silver nanoparticles (Ag-NPs), making it a complete green chemical route. The reduction of Ag+ to Ag0 was observed by the color change from pale yellow to dark yellow. The reaction was followed with the help of UV-Visible spectrometer. Crystal structure was obtained by carrying out X-ray diffraction studies and it showed face centered cubic (fcc) structure. The particle size and morphology were obtained from transmission electron microscopy (TEM) and small angle X-ray scattering (SAXS) studies. An average particle size of 25 nm silver particles could be obtained using this method and the TEM and SAXS data corroborate with each other. PMID:24061881

  14. Comparative Study of Chemical Composition and Biological Activity of Yellow, Green, Brown, and Red Brazilian Propolis

    PubMed Central

    Machado, Christiane Schineider; Mokochinski, João Benhur; de Lira, Tatiana Onofre; de Oliveira, Fátima de Cassia Evangelista; Cardoso, Magda Vieira; Ferreira, Roseane Guimarães; Sawaya, Alexandra Christine Helena Frankland; Ferreira, Antonio Gilberto; Pessoa, Cláudia; Cuesta-Rubio, Osmany; Monteiro, Marta Chagas; de Campos, Mônica Soares

    2016-01-01

    The chemical composition and biological activity of a sample of yellow propolis from Mato Grosso do Sul, Brazil (EEP-Y MS), were investigated for the first time and compared with green, brown, and red types of Brazilian propolis and with a sample of yellow propolis from Cuba. Overall, EEP-Y MS had different qualitative chemical profiles, as well as different cytotoxic and antimicrobial activities when compared to the other types of propolis assessed in this study and it is a different chemotype of Brazilian propolis. Absence of phenolic compounds and the presence of mixtures of aliphatic compounds in yellow propolis were determined by analysing 1H-NMR spectra and fifteen terpenes were identified by GC-MS. EEP-Y MS showed cytotoxic activity against human tumour strain OVCAR-8 but was not active against Gram-negative or Gram-positive bacteria. Our results confirm the difficulty of establishing a uniform quality standard for propolis from diverse geographical origins. The most appropriate pharmacological applications of yellow types of propolis must be further investigated. PMID:27525023

  15. Comparative Study of Chemical Composition and Biological Activity of Yellow, Green, Brown, and Red Brazilian Propolis.

    PubMed

    Machado, Christiane Schineider; Mokochinski, João Benhur; de Lira, Tatiana Onofre; de Oliveira, Fátima de Cassia Evangelista; Cardoso, Magda Vieira; Ferreira, Roseane Guimarães; Sawaya, Alexandra Christine Helena Frankland; Ferreira, Antonio Gilberto; Pessoa, Cláudia; Cuesta-Rubio, Osmany; Monteiro, Marta Chagas; de Campos, Mônica Soares; Torres, Yohandra Reyes

    2016-01-01

    The chemical composition and biological activity of a sample of yellow propolis from Mato Grosso do Sul, Brazil (EEP-Y MS), were investigated for the first time and compared with green, brown, and red types of Brazilian propolis and with a sample of yellow propolis from Cuba. Overall, EEP-Y MS had different qualitative chemical profiles, as well as different cytotoxic and antimicrobial activities when compared to the other types of propolis assessed in this study and it is a different chemotype of Brazilian propolis. Absence of phenolic compounds and the presence of mixtures of aliphatic compounds in yellow propolis were determined by analysing (1)H-NMR spectra and fifteen terpenes were identified by GC-MS. EEP-Y MS showed cytotoxic activity against human tumour strain OVCAR-8 but was not active against Gram-negative or Gram-positive bacteria. Our results confirm the difficulty of establishing a uniform quality standard for propolis from diverse geographical origins. The most appropriate pharmacological applications of yellow types of propolis must be further investigated. PMID:27525023

  16. Multiple sublethal chemicals negatively affect tadpoles of the green frog, Rana clamitans

    USGS Publications Warehouse

    Boone, Michelle D.; Bridges, Christine M.; Fairchild, James F.; Little, Edward E.

    2005-01-01

    Many habitats may be exposed to multiple chemical contaminants, particularly in agricultural areas where fertilizer and pesticide use are common; however, the singular and interactive effects of contaminants are not well understood. The objective of our study was to examine how realistic, sublethal environmental levels of ammonium nitrate fertilizer (0, 10, 20 mg/L and ammonium chloride control) and the common insecticide carbaryl (0 or 2.5 mg/L) individually and interactively affect the development, size, and survival of green frog (Rana clamitans) tadpoles. We reared tadpoles for 95 d in outdoor 1,000-L polyethylene ponds. We found that the combination of carbaryl and nitrate had a negative effect on development and mass of tadpoles compared to the positive effect that either contaminant had alone. Presence of carbaryl was generally associated with short-term increases in algal resources, including ponds exposed to both carbaryl and nitrate. However, with exposure to nitrate and carbaryl, tadpole mass and development were not positively affected as with one chemical stressor alone. The combination of these sublethal contaminants may reduce the ability of amphibians to benefit from food-rich environments or have metabolic costs. Our study demonstrates the importance of considering multiple stressors when evaluating population-level responses.

  17. Time-resolved analysis of the white photoluminescence from chemically synthesized SiCxOy thin films and nanowires

    NASA Astrophysics Data System (ADS)

    Tabassum, Natasha; Nikas, Vasileios; Ford, Brian; Huang, Mengbing; Kaloyeros, Alain E.; Gallis, Spyros

    2016-07-01

    The study reported herein presents results on the room-temperature photoluminescence (PL) dynamics of chemically synthesized SiCxOy≤1.6 (0.19 < x < 0.6) thin films and corresponding nanowire (NW) arrays. The PL decay transients of the SiCxOy films/NWs are characterized by fast luminescence decay lifetimes that span in the range of 350-950 ps, as determined from their deconvoluted PL decay spectra and their stretched-exponential recombination behavior. Complementary steady-state PL emission peak position studies for SiCxOy thin films with varying C content showed similar characteristics pertaining to the variation of their emission peak position with respect to the excitation photon energy. A nearly monotonic increase in the PL energy emission peak, before reaching an energy plateau, was observed with increasing excitation energy. This behavior suggests that band-tail states, related to C-Si/Si-O-C bonding, play a prominent role in the recombination of photo-generated carriers in SiCxOy. Furthermore, the PL lifetime behavior of the SiCxOy thin films and their NWs was analyzed with respect to their luminescence emission energy. An emission-energy-dependent lifetime was observed, as a result of the modulation of their band-tail states statistics with varying C content and with the reduced dimensionality of the NWs.

  18. Syntheses, spectroscopic investigation and electronic properties of two sulfonamide derivatives: A combined experimental and quantum chemical approach

    NASA Astrophysics Data System (ADS)

    Mahmood, Ayyaz; Akram, Tehmina; de Lima, Edna Barboza

    2016-03-01

    Two sulfonamides derivatives, N-phenethyl-4-methylbenzenesulfonamide (1) and N-(4-hydroxyphenethyl)-4-methylbenzenesulfonamide (2), were successfully synthesized and fully characterized using 1H NMR, 13C NMR, FT-IR spectroscopies and elemental analysis. The molecular and electronic structures of the compounds were further investigated using density functional theory calculation at B3LYP and B3PW91 functionals using 6-311++G(d,p) basis set to provide structural and spectroscopic information and guide spectral assignments. The experimental and simulated 1H NMR, 13C NMR and FT-IR spectra were compared and the accuracy was discussed. The conformational analysis was performed in order to find the most stable molecular structure of the compounds. Molecular quantities such as ionization potential, electron affinity, electronegativity, electrophilicity index and chemical hardness and softness were calculated and used as an additional molecular characteristic to predict the stability of the molecules. Electronic properties such Mullikan atomic charges, HOMO, LUMO and HOMO-LUMO energy gaps and molecular electrostatic potential maps predict the large intramolecular charge transfer within the molecules and significant substitution effects.

  19. Preparation, Characterization, and Size Control of Chemically Synthesized CdS Nanoparticles Capped with Poly(ethylene glycol)

    NASA Astrophysics Data System (ADS)

    Seoudi, R.; Allehyani, S. H. A.; Said, D. A.; Lashin, A. R.; Abouelsayed, A.

    2015-10-01

    We prepared cadmium sulfide (CdS) nanoparticles of a specific size via chemical precipitation at room temperature and characterized them using high-resolution transmission electron microscopy, x-ray powder diffraction, ultraviolet-visible spectroscopy, and Fourier-transform infrared (FTIR) measurements. The results showed that the samples were grown with a cubic phase; the particle size could be changed from 2 nm to 4 nm by varying the molar ratios of the precursors (cadmium chloride and sodium sulfide) in the presence of poly(ethylene glycol) (PEG) as an effective capping agent. The optical bandgap of the synthesized nanoparticles was calculated and ranged from 2.73 eV to 2.92 eV depending on the particle size. A large blue-shift from the bulk bandgap (2.42 eV) was observed owing to the quantum size effect. Surface passivation and adsorption of PEG on the CdS nanoparticles was explained on the basis of FTIR measurements; two bands were observed at 476 cm-1 and 622 cm-1, corresponding to cadmium and sulfide stretching vibrations. We conclude that particle size can be controlled by varying the molar ratios of the precursors. Owing to the PEG encapsulation, the as-prepared samples were extremely stable over time.

  20. Chemical Analysis and Aqueous Solution Properties of Charged Amphiphilic Block Copolymers PBA-b-PAA Synthesized by MADIX

    SciTech Connect

    Jacquin,M.; Muller, P.; Talingting-Pabalan, R.; Cottet, H.; Berret, J.; Futterer, T.; Theodoly, O.

    2007-01-01

    We have linked the structural and dynamic properties in aqueous solution of amphiphilic charged diblock copolymers poly(butyl acrylate)-b-poly(acrylic acid), PBA-b-PAA, synthesized by controlled radical polymerization, with the physico-chemical characteristics of the samples. Despite product imperfections, the samples self-assemble in melt and aqueous solutions as predicted by monodisperse microphase separation theory. However, the PBA core are abnormally large; the swelling of PBA cores is not due to AA (the Flory parameter ?PBA/PAA, determined at 0.25, means strong segregation), but to h-PBA homopolymers (content determined by liquid chromatography at the point of exclusion and adsorption transition, LC-PEAT). Beside the dominant population of micelles detected by scattering experiments, capillary electrophoresis CE analysis permitted detection of two other populations, one of h-PAA, and the other of free PBA-b-PAA chains, that have very short PBA blocks and never self-assemble. Despite the presence of these free unimers, the self-assembly in solution was found out of equilibrium: the aggregation state is history dependant and no unimer exchange between micelles occurs over months (time-evolution SANS). The high PBA/water interfacial tension, measured at 20 mN/m, prohibits unimer exchange between micelles. PBA-b-PAA solution systems are neither at thermal equilibrium nor completely frozen systems: internal fractionation of individual aggregates can occur.

  1. Chemically synthesized CdSe quantum dots inhibit growth of human lung carcinoma cells via ROS generation

    PubMed Central

    Jigyasu, Aditya Kumar; Siddiqui, Sahabjada; Lohani, Mohatashim; Khan, Irfan Ali; Arshad, Md

    2016-01-01

    Quantum dots (QDs), semiconducting materials have potential applications in the field of electronic and biomedical applications including cancer therapy. In present study, cadmium selenide (CdSe) QDs were synthesized by chemical method. Octadecene was used as non-coordinating solvent which facilitated the formation of colloidal solutions of nanoparticles. CdSe QDs were characterized by UV-vis spectrometer and transmission electron microscope (TEM). The size measured by TEM was varied between 2-5 nm depending upon temperature. The cytotoxic activity of QDs was monitored by MTT assay, nuclear condensation, ROS activity and DNA fragmentation assay on human lung epithelial A549 cell line. Cells were treated with different concentrations of varying size of CdSe QDs for 24 h. CdSe QDs induced significant (p < 0.05) dose dependent cytotoxicity and this was comparable to the sizes of particles. Smaller particles were more cytotoxic to the large particles. Fluorescence microscopic analysis revealed that QDs induced oxidative stress generating significant ROS level and consequently, induced nuclear condensation and DNA fragmentation. Study suggested the cytotoxicity of CdSe QDs via ROS generation and DNA fragmentation depending upon particles size. PMID:27047318

  2. Metal oxide nanostructures synthesized on flexible and solid substrates and used for catalysts, UV detectors, and chemical sensors

    NASA Astrophysics Data System (ADS)

    Willander, Magnus; Sadollahkhani, Azar; Echresh, Ahmad; Nur, Omer

    2014-03-01

    In this paper we demonstrate the visibility of the low temperature chemical synthesis for developing device quality material grown on flexible and solid substrates. Both colorimetric sensors and UV photodetectors will be presented. The colorimetric sensors developed on paper were demonstrated for heavy metal detection, in particular for detecting copper ions in aqueous solutions. The demonstrated colorimetric copper ion sensors developed here are based on ZnO@ZnS core-shell nanoparticles (CSNPs). These sensors demonstrated an excellent low detection limit of less than 1 ppm of copper ions. Further the colorimetric sensors operate efficiently in a wide pH range between 4 and 11, and even in turbulent water. The CSNPs were additionally used as efficient photocatalytic degradation element and were found to be more efficient than pure ZnO nanoparticles (NPs). Also p-NiO/n-ZnO thin film/nanorods pn junctions were synthesized by a two-step synthesis process and were found to act as efficient UV photodetectors. Additionally we show the effect of the morphology of different CuO nanostructures on the efficiency of photo catalytic degradation of Congo red organic dye.

  3. Annealed Ce3+-doped ZnO flower-like morphology synthesized by chemical bath deposition method

    NASA Astrophysics Data System (ADS)

    Koao, Lehlohonolo F.; Dejene, Francis B.; Tsega, Moges; Swart, Hendrik C.

    2016-01-01

    We have successfully synthesized ZnO:xmol% Ce3+ (0≤x≤10 mol%) doped nanopowders via the chemical bath deposition method (CBD) technique at low temperature (80 °C) and annealed in air at 700 °C. The X-ray diffraction patterns showed that all the undoped and Ce-doped ZnO nanopowders have a hexagonal wurtzite polycrystalline structure with an average crystallite size of about 46 nm. Weak diffraction peaks related mainly to cerium oxide were also detected at higher concentrations of Ce3+ (x=5-10 mol%). The scanning electron microscopy study revealed that the nanopowder samples were assembled in flower-shaped undoped ZnO and pyramid-shaped Ce3+-doped ZnO nanostructures. The UV-vis spectra showed that the absorption edges shifted slightly to the longer wavelengths with the increase in the Ce3+ ions concentration. Moreover, the photoluminescence (PL) results showed a relative weak visible emission for the Ce3+-doped ZnO nanoparticles compared to the undoped ZnO. The effects of Ce3+-doping on the structure and PL of ZnO nanopowders are discussed in detail.

  4. The structural, electrical and magnetoelectric properties of soft-chemically-synthesized SmFeO3 ceramics

    NASA Astrophysics Data System (ADS)

    Sahoo, Sushrisangita; Mahapatra, P. K.; Choudhary, R. N. P.

    2016-01-01

    The structural, electrical and magnetoelectric properties of SmFeO3 ceramic samples, synthesized using a soft-chemical method, were studied. A structural analysis of the material was carried out by the Rietveld refinement of room temperature x-ray diffraction data. The temperature dependence of the dielectric peaks was analyzed by fitting them with two Gaussian peaks corresponding to two phase transitions—one being electric, and the other being magnetic in nature. The depression angle of the semicircles in a Nyquist plot representing the grain and grain boundary contributions in the sample was estimated. The grain boundary effect, appearing at temperatures above 75 °C, is explained using the Maxwell-Wagner mechanism. The impedance study reveals a semi-conducting grain with an insulating grain boundary, leading to the formation of surface and internal barrier layer capacitors and resulting in a very high dielectric constant. The effect of dc conductivity on the loss tangent at low frequencies and high temperature has been analyzed. The frequency dependence of ac conductivity in the two different regions can be explained on the basis of correlated barrier hopping and quantum mechanical tunneling models. The material is found to exhibit canted antiferromagnetism and improper ferroelectric characteristics. The value of the magnetoelectric voltage-coupling coefficient (α) of a SmFeO3 ceramic is found to be 2.2 mV cm-1 Oe-1.

  5. Chemical characterization of orange juice from trees infected with citrus greening (Huanglongbing).

    PubMed

    Dagulo, Lilibeth; Danyluk, Michelle D; Spann, Timothy M; Valim, M Filomena; Goodrich-Schneider, Renée; Sims, Charles; Rouseff, Russell

    2010-03-01

    The effects due to Candidatus Liberibacter infection, commonly called citrus greening or Huanglongbing (HLB), on volatile and nonvolatile components of orange juices, OJ, were examined using GC-MS and high-performance liquid chromatography (HPLC). HLB symptomatic, asymptomatic, and control "Hamlin" and "Valencia" oranges were harvested from December to May during the 2007 to 2008 harvest season. Brix/acid levels in control and asymptomatic juices were similar but symptomatic juices were as much as 62% lower than control juices. No bitter flavanone neohesperidosides were detected and polymethoxyflavone concentrations were well below bitter taste thresholds. Limonin concentrations were significantly higher (91% to 425%) in symptomatic juice compared to control but still below juice bitterness taste thresholds. Juice terpenes, such as gamma-terpinene and alpha-terpinolene, were as much as 1320% and 62% higher in symptomatic juice than control. Average ethyl butanoate concentrations were 45% lower and average linalool was 356% higher in symptomatic Valencia OJ compared to control. Symptomatic Valencia OJ had on average only 40% the total esters, 48% the total aldehydes, and 33% as much total sesquiterpenes as control juice. Total volatiles between control and symptomatic juices were similar due to elevated levels of alcohols and terpenes in symptomatic juice. There were no consistent differences between asymptomatic and control juices. The chemical composition of juice from HLB/greening symptomatic fruit appears to mimic that of juice from less mature fruit. The reported off-flavor associated with symptomatic juices probably stem from lower concentrations of sugars, higher concentrations of acid as all known citrus bitter compounds were either below taste thresholds or absent. PMID:20492226

  6. CHEMICAL AND MINERALOGICAL CHARACTERISTICS OF FRENCH GREEN CLAYS USED FOR HEALING.

    PubMed

    Williams, Lynda B; Haydel, Shelley E; Giese, Rossman F; Eberl, Dennis D

    2008-08-01

    The worldwide emergence of infectious diseases, together with the increasing incidence of antibiotic-resistant bacteria, elevate the need to properly detect, prevent, and effectively treat these infections. The overuse and misuse of common antibiotics in recent decades stimulates the need to identify new inhibitory agents. Therefore, natural products like clays, that display antibacterial properties, are of particular interest.The absorptive properties of clay minerals are well documented for healing skin and gastrointestinal ailments. However, the antibacterial properties of clays have received less scientific attention. French green clays have recently been shown to heal Buruli ulcer, a necrotic or 'flesh-eating' infection caused by Mycobacterium ulcerans. Assessing the antibacterial properties of these clays could provide an inexpensive treatment for Buruli ulcer and other skin infections.Antimicrobial testing of the two clays on a broad-spectrum of bacterial pathogens showed that one clay promotes bacterial growth (possibly provoking a response from the natural immune system), while another kills bacteria or significantly inhibits bacterial growth. This paper compares the mineralogy and chemical composition of the two French green clays used in the treatment of Buruli ulcer.Mineralogically, the two clays are dominated by 1Md illite and Fe-smectite. Comparing the chemistry of the clay minerals and exchangeable ions, we conclude that the chemistry of the clay, and the surface properties that affect pH and oxidation state, control the chemistry of the water used to moisten the clay poultices and contribute the critical antibacterial agent(s) that ultimately debilitate the bacteria. PMID:19079803

  7. CHEMICAL AND MINERALOGICAL CHARACTERISTICS OF FRENCH GREEN CLAYS USED FOR HEALING

    PubMed Central

    Williams, Lynda B.; Haydel, Shelley E.; Giese, Rossman F.; Eberl, Dennis D.

    2008-01-01

    The worldwide emergence of infectious diseases, together with the increasing incidence of antibiotic-resistant bacteria, elevate the need to properly detect, prevent, and effectively treat these infections. The overuse and misuse of common antibiotics in recent decades stimulates the need to identify new inhibitory agents. Therefore, natural products like clays, that display antibacterial properties, are of particular interest. The absorptive properties of clay minerals are well documented for healing skin and gastrointestinal ailments. However, the antibacterial properties of clays have received less scientific attention. French green clays have recently been shown to heal Buruli ulcer, a necrotic or ‘flesh-eating’ infection caused by Mycobacterium ulcerans. Assessing the antibacterial properties of these clays could provide an inexpensive treatment for Buruli ulcer and other skin infections. Antimicrobial testing of the two clays on a broad-spectrum of bacterial pathogens showed that one clay promotes bacterial growth (possibly provoking a response from the natural immune system), while another kills bacteria or significantly inhibits bacterial growth. This paper compares the mineralogy and chemical composition of the two French green clays used in the treatment of Buruli ulcer. Mineralogically, the two clays are dominated by 1Md illite and Fe-smectite. Comparing the chemistry of the clay minerals and exchangeable ions, we conclude that the chemistry of the clay, and the surface properties that affect pH and oxidation state, control the chemistry of the water used to moisten the clay poultices and contribute the critical antibacterial agent(s) that ultimately debilitate the bacteria. PMID:19079803

  8. Chemical and mineralogical characteristics of French green clays used for healing

    USGS Publications Warehouse

    Williams, L.B.; Haydel, S.E.; Giese, R.F.; Eberl, D.D.

    2008-01-01

    The worldwide emergence of infectious diseases, together with the increasing incidence of antibiotic-resistant bacteria, elevate the need to properly detect, prevent, and effectively treat these infections. The overuse and misuse of common antibiotics in recent decades stimulates the need to identify new inhibitory agents. Therefore, natural products like clays, that display antibacterial properties, are of particular interest. The absorptive properties of clay minerals are well documented for healing skin and gastrointestinal ailments. However, the antibacterial properties of clays have received less scientific attention. French green clays have recently been shown to heal Buruli ulcer, a necrotic or 'flesh-eating' infection caused by Mycobacterium ulcerans. Assessing the antibacterial properties of these clays could provide an inexpensive treatment for Buruli ulcer and other skin infections. Antimicrobial testing of the two clays on a broad-spectrum of bacterial pathogens showed that one clay promotes bacterial growth (possibly provoking a response from the natural immune system), while another kills bacteria or significantly inhibits bacterial growth. This paper compares the mineralogy and chemical composition of the two French green clays used in the treatment of Buruli ulcer. Mineralogically, the two clays are dominated by 1Md illite and Fe-smectite. Comparing the chemistry of the clay minerals and exchangeable ions, we conclude that the chemistry of the clay, and the surface properties that affect pH and oxidation state, control the chemistry of the water used to moisten the clay poultices and contribute the critical antibacterial agent(s) that ultimately debilitate the bacteria. Copyright ?? 2008, The Clay Minerals Society.

  9. A novel pyrophosphate BaCr2(P2O7)2 as green pigment with high NIR solar reflectance and durable chemical stability

    NASA Astrophysics Data System (ADS)

    Tao, Zhengxu; Zhang, Wanqi; Huang, Yanlin; Wei, Donglei; Seo, Hyo Jin

    2014-08-01

    A novel pyrophosphate BaCr2(P2O7)2 was synthesized by the conventional solid-state reaction. The X-ray diffraction (XRD), FTIR spectrum, scanning electron microscopy (SEM) and ultraviolet-visible (UV-Vis) near infrared (NIR) reflectance spectra were applied to characterize the powders. The refractive indexes and nature of the VB and CB were determined. The structure, color properties and application were investigated. The results reveal that the anomalist bodies with smooth surfaces were obtained at 1200 °C with a mean size of 3 μm. A high reflectance peak at 535 nm was observed in the visible region, which is associated with the brilliant and deep green color of this pigment. With all the acids, alkali and deionized water treatment, the polycrystalline pigment BaCr2(P2O7)2 was found to be durable in chemical stability. The significantly high NIR solar reflectance of BaCr2(P2O7)2 is 90.0%, a higher cooling ability, so it has been selected to be tested as cool green pigment in ceramics. Moreover, this novel pyrophosphate pigment has great potential as cool pigment for surface coating applications.

  10. Cross-linking and ultrathin grafted gradation of fluorinated polymers synthesized via initiated chemical vapor deposition to prevent surface reconstruction.

    PubMed

    Liu, Andong; Goktekin, Esma; Gleason, Karen K

    2014-12-01

    Poly(fluoroalkyl acrylate)s with long perfluorooctyl pendant groups have been found to lead to the release of biopersistent perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS). Those with no more than six perfluorinated carbons in pedant groups do not cause such problems. They, however, give poor dynamic water repellency due to extensive reorganization of surface fluorinated groups when exposed to the water interface. In this work, thin films exhibiting improved dynamic water repellency, as evidenced by water contact angle (WCA) measurements, were synthesized via substrate-independent initiated chemical vapor deposition (iCVD) from 1H,1H,2H,2H-perfluorooctyl acrylate (C6PFA) and divinylbenzene (DVB) using two methods: copolymerization and ultrathin grafted gradation. The copolymerization between C6PFA and the cross-linker, DVB, was confirmed by Fourier transform infrared (FTIR) spectroscopy. The cross-linking is concluded to hinder the reorganization of surface fluorinated groups. The grafted gradation, consisting of an ultrathin pC6PFA top layer and a pDVB base layer, was characterized by angle-resolved X-ray photoelectron spectroscopy (ARXPS) measurements, which indicated that the top layer of pC6PFA is <2.5 nm thick to achieve the best dynamic water repellency. The outmost surface of this structure is fully covered by fluorinated groups, giving hydrophobicity. Concurrently, thanks to the interlayer grafting and the ultrathinness of the top layer, the fluorinated groups' tendency to migrate away from water interface is sterically blocked by the highly cross-linked pDVB base layer. The proposed approaches effectively reduced WCA hysteresis of C6PFA-based thin film to as low as 26.9° while maintaining sufficient hydrophobicity (advanced WCA of 119.6°). Due to the conformal and substrate-independent nature of iCVD technique, the films could be used to coat textured surfaces to generate superhydrophobicity. PMID:25358035

  11. Characterization of atomic-layer MoS2 synthesized using a hot filament chemical vapor deposition method

    NASA Astrophysics Data System (ADS)

    Ying-Zi, Peng; Yang, Song; Xiao-Qiang, Xie; Yuan, Li; Zheng-Hong, Qian; Ru, Bai

    2016-05-01

    Atomic-layer MoS2 ultrathin films are synthesized using a hot filament chemical vapor deposition method. A combination of atomic force microscopy (AFM), x-ray diffraction (XRD), high-resolution transition electron microscopy (HRTEM), photoluminescence (PL), and x-ray photoelectron spectroscopy (XPS) characterization methods is applied to investigate the crystal structures, valence states, and compositions of the ultrathin film areas. The nucleation particles show irregular morphology, while for a larger size somewhere, the films are granular and the grains have a triangle shape. The films grow in a preferred orientation (002). The HRTEM images present the graphene-like structure of stacked layers with low density of stacking fault, and the interlayer distance of plane is measured to be about 0.63 nm. It shows a clear quasi-honeycomb-like structure and 6-fold coordination symmetry. Room-temperature PL spectra for the atomic layer MoS2 under the condition of right and left circular light show that for both cases, the A1 and B1 direct excitonic transitions can be observed. In the meantime, valley polarization resolved PL spectra are obtained. XPS measurements provide high-purity samples aside from some contaminations from the air, and confirm the presence of pure MoS2. The stoichiometric mole ratio of S/Mo is about 2.0–2.1, suggesting that sulfur is abundant rather than deficient in the atomic layer MoS2 under our experimental conditions. Project supported by the Natural Science Foundation of Zhejiang Province, China (Grant Nos. LY16F040003 and LY16A040007) and the National Natural Science Foundation of China (Grant Nos. 51401069 and 11574067).

  12. Supported gold catalysis: from small molecule activation to green chemical synthesis.

    PubMed

    Liu, Xiang; He, Lin; Liu, Yong-Mei; Cao, Yong

    2014-03-18

    With diminishing natural resources, there is an ever-increasing demand for cost-effective and sustainable production of fine and commodity chemicals. For this purpose, there is a need for new catalytic methods that can permit efficient and targeted conversion of fossil and biorenewable feedstocks with lower energy requirements and environmental impact. A significant number of industrial catalytic processes are performed by platinum-group-metal (PGM)-based heterogeneous catalysts capable of activating a range of important small molecules, such as CO, O2, H2, and N2. In contrast, there is a general feeling that gold (Au) cannot act as an efficient catalyst because of its inability to activate most molecules, which is essential to any catalytic processes. As a consequence, researchers have long neglected the potential for use of gold as a catalyst. In recent years, however, chemists have put forth tremendous effort and progress in the use of supported gold catalysts to facilitate a variety of useful synthetic transformations. The seminal discovery by Haruta in 1987 that suitably prepared Au-based catalysts were surprisingly active for CO oxidation even at 200 K initiated rapid development of the field. Since then, researchers have widely employed Au-based catalysts in many types of mild chemical processes, with special focus on selective reactions involving small molecules (for example, CO, H2O, O2, or H2) as a reactant. That gold in the form of tiny nanoparticles (NPs, generally less than 5 nm in diameter) can subtly activate the reactant molecules under mild conditions has been evoked to explain the superior effectiveness of gold compared with conventional PGMs. In this context, Au-based catalysts are gaining great significance in developing new green processes with improved selectivity and energy minimization. In this Account, we describe our efforts toward the development of a range of green and selective processes largely through the appropriate choice of Au

  13. Physiological and physico-chemical characterization of dietary fibre from the green seaweed Ulva fasciata Delile.

    PubMed

    Carvalho, A F U; Portela, M C C; Sousa, M B; Martins, F S; Rocha, F C; Farias, D F; Feitosa, J P A

    2009-08-01

    This work aims to assess the potential of the green seaweed Ulva fasciata Delile as an alternative source of dietary fibre (DF). Total DF content was determined, some of its physico-chemical properties described and the physiological effects of U. fasciata meal on rats fed a hypercholesterolemic diet were investigated. U. fasciata may be considered a potential alternative source of DF with a total content of about 400 g.kg-1 (dry basis) and interesting physico-chemical properties: water retention capacity of 8.74 g/water.g-1 dry sample (seaweed meal) and 0.90 (seaweed carbohydrate extract), lipid adsorption capacity of 4.52 g/oil.g-1 dry sample (seaweed meal) and 5.70 (seaweed carbohydrate extract), intrinsic viscosity of 2.4 dl.g-1 (seaweed carbohydrate extract) and cation exchange capacity of 3.51 Eq.kg-1 (seaweed carbohydrate extract). The diet containing seaweed meal was able to keep rats' total cholesterol (TC) down without causing any undesirable increase in LDL-C fraction. No evidence of toxic and/or antinutritional components in the seaweed meal was detected. Rats showed a fecal volume much greater (13 g) than that fed on cellulose diet (7 g) (p < 0.05). These properties confer on the seaweed the potential to be used in food technology for the acquisition of low-calorie food and might be important in body weight control, reduction of blood TC and LDL-C as well as in prevention of gastrointestinal diseases. PMID:19802460

  14. Effects of green liquor pretreatment on the chemical composition and enzymatic digestibility of rice straw.

    PubMed

    Gu, Feng; Wang, Wangxia; Jing, Lei; Jin, Yongcan

    2013-12-01

    Green liquor (Na2S+Na2CO3, GL) pretreatment is a proven pathway to improve the enzymatic saccharification for the production of bioethanol. In this work, the effects of GL pretreatment on the chemical composition and enzymatic digestibility of rice straw at various total titratable alkali (TTA) charge and temperature were investigated. The GL pretreatment showed excellent performance in high polysaccharides retention and delignification selectivity. Under the optimized GL pretreatment condition (4% TTA charge, 20% sulfidity and 140°C), 92.5% of glucan, 82.4% of xylan and 81.6% of arabinan in rice straw were recovered with a delignification of 39.4%. The maximum sugar yields of 83.9%, 69.6% and 78.0%, respectively for glucan, xylan and total sugar, were achieved at the same GL pretreatment condition with an enzyme loading of 40 FPU/g-substrate. The results suggested that GL pretreatment is a practicable method for rice straw to enhance enzymatic saccharification for bioethanol production. PMID:24128400

  15. Preparation of intact chloroplasts by chemically induced lysis of the green alga Dunaliella marina.

    PubMed

    Kombrink, E; Wöber, G

    1980-07-01

    A method for the isolation in high yield of intact chloroplasts from the unicellular green alga Dunaliella marina (Volvocales) is described. This procedure uses chemically induced lysis of cells with the polycationic macromolecules, DEAE-dextran (M=500,000) or poly-D,L-lysine (M=30,000-70,000). Reaction conditions were optimized with respect to obtaining a high yield of intact chloroplasts, after isopycnic centrifugation in a linear sucrose density gradient, by varying the concentration of polycation and the temperature and pH of incubation. Broken chloroplasts devoid of the stromal marker enzymes fructosebisphosphate phosphatase and ribulosebisphosphate carboxylase, but containing mitochondrial (fumarase) and microbody (catalase) contamination, were banded at a bouyant density of 1.18 g cm(-3). Intact chloroplasts, as indicated by their retention of alkaline fructosebisphosphate phosphatase and ribulosebisphosphate carboxylase, were found in 30% yield (chlorophyll in intact cells, 100%) at an equilibrium density of 1.24 g cm(-3). Contamination by cytoplasmic material (pyruvate kinase), mitochondria, and microbodies was less than 8% each. PMID:24306242

  16. A non-targeted approach to chemical discrimination between green tea dietary supplements and green tea leaves by HPLC/MS.

    PubMed

    Sun, Jianghao; Chen, Pei; Lin, Long-Ze; Harnly, James M

    2011-01-01

    Green tea-based dietary supplements (GTDSs) have gained popularity in the U.S. market in recent years. This study evaluated the phytochemical composition difference of GTDS in comparison with green tea leaves using an HPLC/MS fingerprinting technique coupled with chemometric analysis. Five components that are most responsible for class separation among samples were identified as (-) epicatechin gallate, strictinin, trigalloylglucose, quercetin-3-O-glucosyl-rhamnosylglucoside, and kaempferol-3-O-galactosyl-rhamnosylglucoside, according to the accurate mass measurements and MS/MS data. The similarity coefficients between the GTDSs in solid form with green tea were 0.55 to 0.91, while for the GTDSs in liquid form they were 0.12 to 0.89, which suggested that chemical composition variance across the GTDSs was significant. Flavonol aglycone concentrations were higher in GTDSs than in tea leaves, indicating the degradation of flavonol glycosides or the oxidation of catechin during the manufacturing and storage processes. In some GTDS samples, compounds were identified that were on the label. The results demonstrate the urgency of QC for GTDS products. PMID:21563682

  17. A Non-targeted Approach to Chemical Discrimination Between Green Tea Dietary Supplements and Green Tea Leaves by HPLC/MS

    PubMed Central

    Sun, Jianghao; Chen, Pei; Lin, Long-Ze; Harnly, James M.

    2013-01-01

    Green tea-based dietary supplements (GTDSs) have gained popularity in the U.S. market in recent years. This study evaluated the phytochemical composition difference of GTDS in comparison with green tea leaves using an HPLC/MS fingerprinting technique coupled with chemometric analysis. Five components that are most responsible for class separation among samples were identified as (−) epicatechin gallate, strictinin, trigalloylglucose, quercetin-3-O-glucosylrhamnosylglucoside, and kaempferol-3-O-galactosyl-rhamnosylglucoside, according to the accurate mass measurements and MS/MS data. The similarity coefficients between the GTDSs in solid form with green tea were 0.55 to 0.91, while for the GTDSs in liquid form they were 0.12 to 0.89, which suggested that chemical composition variance across the GTDSs was significant. Flavonol aglycone concentrations were higher in GTDSs than in tea leaves, indicating the degradation of flavonol glycosides or the oxidation of catechin during the manufacturing and storage processes. In some GTDS samples, compounds were identified that were on the label. The results demonstrate the urgency of QC for GTDS products. PMID:21563682

  18. Solvent resistant microfluidic DNA synthesizer.

    PubMed

    Huang, Yanyi; Castrataro, Piero; Lee, Cheng-Chung; Quake, Stephen R

    2007-01-01

    We fabricated a microfluidic DNA synthesizer out of perfluoropolyether (PFPE), an elastomer with excellent chemical compatibility which makes it possible to perform organic chemical reactions, and synthesized 20-mer oligonucleotides on chip. PMID:17180201

  19. Dietary supplementation of green synthesized manganese-oxide nanoparticles and its effect on growth performance, muscle composition and digestive enzyme activities of the giant freshwater prawn Macrobrachium rosenbergii.

    PubMed

    Asaikkutti, Annamalai; Bhavan, Periyakali Saravana; Vimala, Karuppaiya; Karthik, Madhayan; Cheruparambath, Praseeja

    2016-05-01

    The green synthesized Mn3O4 nanoparticles (manganese-oxide nanoparticles) using Ananas comosus (L.) peel extract was characterized by various techniques. HR-SEM photograph showed that manganese-oxide nanoparticles (Mn-oxide NPs) were spherical in shape, with an average size of 40-50 nm. The Zeta potential revealed the surface charge of Mn-oxide NPs to be negative. Further, the Mn-oxide NPs were dietary supplemented for freshwater prawn Macrobrachium rosenbergii. The experimental basal diets were supplemented with Mn-oxide NPs at the rates of 0 (control), 3.0, 6.0, 9.0, 12, 15 and 18 mg/kg dry feed weight. The as-supplemented Mn-oxide NPs were fed in M. rosenbergii for a period of 90 days. The experimental study demonstrated that prawns fed with diet supplemented with 3-18 mg Mn-oxide NPs/kg shows enhanced (P<0.05) growth performance, including final weight and weight gain (WG). Significant differences (P<0.05) in feed conversion ratio (FCR) were observed in prawn fed with different diets. Additionally, prawns fed with 3.0-18 mg/kg Mn-oxide NPs supplemented diets achieved significant (P<0.05) improvement in growth performance, digestive enzyme activities and muscle biochemical compositions, while, the prawns fed with 16 mg/kg of Mn-oxide NPs showed enhanced performance. Prawns fed on diet supplemented with 16 mg/kg Mn-oxide NPs showed significantly (P<0.05) higher total protein level. The antioxidants enzymatic activity (SOD and CAT) metabolic enzymes status in muscle and hepatopancreas showed no significant (P>0.05) alterations in prawns fed with 3.0-18 mg/kg of Mn-oxide NPs supplemented diets. Consequently, the present work proposed that 16 mg/kg of Mn-oxide NPs could be supplemented for flexible enhanced survival, growth and production of M. rosenbergii. Therefore, the data of the present study recommend the addition of 16 mg/kg of Mn-oxide NPs diet to developed prawn growth and antioxidant defense system. PMID:27049122

  20. Comparison of the nutrient and chemical contents of traditional Korean Chungtaejeon and green teas.

    PubMed

    Park, Yong-Seo; Lee, Mi-Kyung; Heo, Buk-Gu; Ham, Kyung-Sik; Kang, Seong-Gook; Cho, Ja-Yong; Gorinstein, Shela

    2010-06-01

    This study was conducted in order to compare the nutrient and chemical contents of two Korean teas: traditional Chungtaejeon tea (CTJ) with that of green tea (GT). Main bioactive compounds and the antioxidant activities using four radical scavenging assays (ABTS, CUPRAC, FRAP and DPPH) in methanol and acetone extracts of both teas were determined. It was found that the contents of vitamin C, amino acids and total nitrogen in CTJ were lower than that of GT (p < 0.05). Caffeine, reducing sugar and chlorophyll contents in CTJ were similar to GT. Catechin (C), epicatechin (EC), and epigallocatechin (EGC) contents were lower in CTJ than in green tea (p < 0.05), but gallocatechin (GC), epicatechin gallate (ECG), epigallocatechin gallate (EGCG) and catechin gallate (CG) showed no significant differences between CTJ and GT (p >/= 0.05). The contents of polyphenols, flavonoids, flavanols and tannins in CTJ methanol were 229.30 +/- 11.3 mg GAE/g dry weight (DW), 15.24 +/- 0.8 mg CE/g DW, 109.10 +/- 5.1 mg CE/g DW and 25.68 +/- 1.2 mg CE/g DW, respectively, and significantly higher than in acetone extracts (p < 0.05). Flavonoids (quercetin and kaempferol) were higher in GT than in CTJ and myricetin was higher in CTJ (p < 0.05). Threonine and aspartic acid was lower, and glutamic acid was higher in CTJ compared with GT (p < 0.05). Free amino acid content in CTJ and GT showed no significant difference. Potassium and magnesium in CTJ were lower compared to GT, but no significant difference was found for iron, manganese and calcium. Also, the level of the antioxidant activity by all four used assays was significantly higher in CTJ and in methanol was higher than in acetone extracts (p < 0.05). In conclusion, traditional fermented Korean tea Chungtaejeon contains high quantities of bioactive compounds and possesses high antioxidant activity. The contents of the bioactive compounds and the levels of antioxidant activities are significantly higher in methanol than in acetone

  1. Discrimination of the production season of Chinese green tea by chemical analysis in combination with supervised pattern recognition.

    PubMed

    Xu, Wenping; Song, Qiushuang; Li, Daxiang; Wan, Xiaochun

    2012-07-18

    High-performance liquid chromatography (HPLC) has been used to quantify levels of free amino acids, catechins, and caffeine in Chinese green tea. Levels of free amino acids and catechins in green tea leaves show obvious variation from spring to summer, which is useful information to identify the production season of commercial green tea. Supervised pattern recognition methods such as the K-nearest neighbor (KNN) method and Bayesian discriminant method (a type of linear discriminant analysis (LDA)) were used to discriminate between the production seasons of Chinese green tea. The optimal accuracy of the KNN method was ≤97.61 and ≤94.80% as validated by resubstitution and cross-validation tests, respectively, and that of LDA was ≤95.22 and ≤93.54%, respectively. Compared with LDA, the KNN method did not require a Gaussian distribution and was more accurate than LDA. The KNN method in combination with chemical analysis is recommended for discrimination of the production seasons of Chinese green tea. PMID:22720840

  2. Chemical concentrations and instantaneous loads, Green River to the Lower Duwamish Waterway near Seattle, Washington, 2013–15

    USGS Publications Warehouse

    Conn, Kathleen E.; Black, Robert W.; Vanderpool-Kimura, Ann M.; Foreman, James R.; Peterson, Norman T.; Senter, Craig A.; Sissel, Stephen K.

    2015-01-01

    Median chemical concentrations in suspended-sediment samples were greater than median chemical concentrations in fine bed sediment (less than 62.5 µm) samples, which were greater than median chemical concentrations in paired bulk bed sediment (less than 2 mm) samples. Suspended-sediment concentration, sediment particle-size distribution, and general water-quality parameters were measured concurrent with the chemistry sampling. From this discrete data, combined with the continuous streamflow record, estimates of instantaneous sediment and chemical loads from the Green River to the Lower Duwamish Waterway were calculated. For most compounds, loads were higher during storms than during baseline conditions because of high streamflow and high chemical concentrations. The highest loads occurred during dam releases (periods when stored runoff from a prior storm is released from the Howard Hanson Dam into the upper Green River) because of the high river streamflow and high suspended-sediment concentration, even when chemical concentrations were lower than concentrations measured during storm events. 

  3. CHEMICAL INTERACTIONS OF ARSENATE, ARSENITE, PHOSPHATE, AND SILICATE WITH IRON (II, III) HYDROXYCARBONATE GREEN RUST

    EPA Science Inventory

    Granular zerovalent iron has been proposed to be used as a medium in permeable reactive barriers (PRBs) to remove arsenic from contaminated groundwater. Iron(II, III) hydroxycarbonate green rust (carbonate green rust, or CGR) is a major corrosion product of zerovalent iron under ...

  4. CHEMICAL INTERACTIONS OF ARSENATE, ARSENITE, PHOSPHATE, AND SILICATE WITH IRON (II,III) HYDROXYCARBONATE GREEN RUST

    EPA Science Inventory

    Granular zerovalent iron has been proposed to be used as a medium in permeable reactive barriers (PRBs) to remove arsenic from contaminated groundwater. Iron(II, III) hydroxycarbonate green rust (carbonate green rust, or CGR) is a major corrosion product of zerovalent iron under ...

  5. Chemical induction of endogenous retrovirus particles from the vero cell line of African green monkeys.

    PubMed

    Ma, Hailun; Ma, Yunkun; Ma, Wenbin; Williams, Dhanya K; Galvin, Teresa A; Khan, Arifa S

    2011-07-01

    Endogenous retroviral sequences are present in high copy numbers in the genomes of all species and may be expressed as RNAs; however, the majority are defective for virus production. Although virus has been isolated from various Old World monkey and New World monkey species, there has been no report of endogenous retroviruses produced from African green monkey (AGM) tissues or cell lines. We have recently developed a stepwise approach for evaluating the presence of latent viruses by chemical induction (Khan et al., Biologicals 37:196-201, 2009). Based upon this strategy, optimum conditions were determined for investigating the presence of inducible, endogenous retroviruses in the AGM-derived Vero cell line. Low-level reverse transcriptase activity was produced with 5-azacytidine (AzaC) and with 5'-iodo-2'-deoxyuridine (IUdR); none was detected with sodium butyrate. Nucleotide sequence analysis of PCR-amplified fragments from the gag, pol, and env regions of RNAs, prepared from ultracentrifuged pellets of filtered supernatants, indicated that endogenous retrovirus particles related to simian endogenous type D betaretrovirus (SERV) sequences and baboon endogenous virus type C gammaretrovirus (BaEV) sequences were induced by AzaC, whereas SERV sequences were also induced by IUdR. Additionally, sequence heterogeneity was seen in the RNAs of SERV- and BaEV-related particles. Infectivity analysis of drug-treated AGM Vero cells showed no virus replication in cell lines known to be susceptible to type D simian retroviruses (SRVs) and to BaEV. The results indicated that multiple, inducible endogenous retrovirus loci are present in the AGM genome that can encode noninfectious, viruslike particles. PMID:21543506

  6. Automatic chemical structure annotation of an LC-MS(n) based metabolic profile from green tea.

    PubMed

    Ridder, Lars; van der Hooft, Justin J J; Verhoeven, Stefan; de Vos, Ric C H; Bino, Raoul J; Vervoort, Jacques

    2013-06-18

    Liquid chromatography coupled with multistage accurate mass spectrometry (LC-MS(n)) can generate comprehensive spectral information of metabolites in crude extracts. To support structural characterization of the many metabolites present in such complex samples, we present a novel method ( http://www.emetabolomics.org/magma ) to automatically process and annotate the LC-MS(n) data sets on the basis of candidate molecules from chemical databases, such as PubChem or the Human Metabolite Database. Multistage MS(n) spectral data is automatically annotated with hierarchical trees of in silico generated substructures of candidate molecules to explain the observed fragment ions and alternative candidates are ranked on the basis of the calculated matching score. We tested this method on an untargeted LC-MS(n) (n ≤ 3) data set of a green tea extract, generated on an LC-LTQ/Orbitrap hybrid MS system. For the 623 spectral trees obtained in a single LC-MS(n) run, a total of 116,240 candidate molecules with monoisotopic masses matching within 5 ppm mass accuracy were retrieved from the PubChem database, ranging from 4 to 1327 candidates per molecular ion. The matching scores were used to rank the candidate molecules for each LC-MS(n) component. The median and third quartile fractional ranks for 85 previously identified tea compounds were 3.5 and 7.5, respectively. The substructure annotations and rankings provided detailed structural information of the detected components, beyond annotation with elemental formula only. Twenty-four additional components were putatively identified by expert interpretation of the automatically annotated data set, illustrating the potential to support systematic and untargeted metabolite identification. PMID:23662787

  7. Chemical Induction of Endogenous Retrovirus Particles from the Vero Cell Line of African Green Monkeys▿

    PubMed Central

    Ma, Hailun; Ma, Yunkun; Ma, Wenbin; Williams, Dhanya K.; Galvin, Teresa A.; Khan, Arifa S.

    2011-01-01

    Endogenous retroviral sequences are present in high copy numbers in the genomes of all species and may be expressed as RNAs; however, the majority are defective for virus production. Although virus has been isolated from various Old World monkey and New World monkey species, there has been no report of endogenous retroviruses produced from African green monkey (AGM) tissues or cell lines. We have recently developed a stepwise approach for evaluating the presence of latent viruses by chemical induction (Khan et al., Biologicals 37:196–201, 2009). Based upon this strategy, optimum conditions were determined for investigating the presence of inducible, endogenous retroviruses in the AGM-derived Vero cell line. Low-level reverse transcriptase activity was produced with 5-azacytidine (AzaC) and with 5′-iodo-2′-deoxyuridine (IUdR); none was detected with sodium butyrate. Nucleotide sequence analysis of PCR-amplified fragments from the gag, pol, and env regions of RNAs, prepared from ultracentrifuged pellets of filtered supernatants, indicated that endogenous retrovirus particles related to simian endogenous type D betaretrovirus (SERV) sequences and baboon endogenous virus type C gammaretrovirus (BaEV) sequences were induced by AzaC, whereas SERV sequences were also induced by IUdR. Additionally, sequence heterogeneity was seen in the RNAs of SERV- and BaEV-related particles. Infectivity analysis of drug-treated AGM Vero cells showed no virus replication in cell lines known to be susceptible to type D simian retroviruses (SRVs) and to BaEV. The results indicated that multiple, inducible endogenous retrovirus loci are present in the AGM genome that can encode noninfectious, viruslike particles. PMID:21543506

  8. A molecular line study towards massive extended green object clumps in the southern sky: chemical properties

    NASA Astrophysics Data System (ADS)

    Yu, Naiping; Wang, Jun-Jie

    2015-08-01

    We present a molecular line study towards 31 extended green object (EGO) clumps in the southern sky using data from MALT90 (Millimetre Astronomy Legacy Team 90 GHz). According to previous multiwavelength observations, we divide our sample into two groups: massive young stellar objects (MYSOs) and H II regions. The most detected lines are N2H+ (J = 1 - 0), HCO+ (J = 1 - 0), HNC (J = 1 - 0), HCN (J = 1 - 0), HC3N (J = 10 - 9), H13CO+ (J = 1 - 0), C2H (N = 1 - 0) and SiO (J = 2 - 1), indicating that most EGOs are indeed associated with dense clumps and recent outflow activities. The velocity widths of the N2H+ (J = 1 - 0), H13CO+ (J = 1 - 0), C2H (N = 1 - 0) and HC3N (J = 10 - 9) lines are comparable to each other in MYSOs. However, in H II regions the velocity widths of the N2H+ (J = 1 - 0) and C2H (N = 1 - 0) lines tend to be narrower than those of H13CO+ (J = 1 - 0) and HC3N (J = 10 - 9). Our results seem to support that N2H+ and C2H emissions mainly come from the gas inside quiescent clumps. In addition, we also find that the [N2H+]/[H13CO+] and [C2H]/[H13CO+] relative abundance ratios decrease from MYSOs to H II regions. These results suggest depletion of N2H+ and C2H in the late stages of massive-star formation, probably caused by the formation of H II regions inside. N2H+ and C2H might be used as chemical clocks for massive-star formation by comparing with other molecules such as H13CO+ and HC3N.

  9. "Green" synthesized and coated nanaosilver alters the membrance permeability of barrier (intestinal, brain, endothelial) cells and stimulates oxidative stress pathways in neurons.

    EPA Science Inventory

    Nanosilver's (nanoAg) use in medical applications and consumer products is increasing. Because of this, its "green" synthesis and surface modification with beneficial coatings are desirable. Given nanoAg's potential exposure routes (e.g., dermal, intestin...

  10. Effects of size-controlled TiO2 nanopowders synthesized by chemical vapor condensation process on conversion efficiency of dye-sensitized solar cells.

    PubMed

    Kim, Woo-Byoung; Lee, Jai-Sung

    2013-07-01

    To investigate the microstructural effects of the synthesized TiO2 nanopowders such as particle size, specific surface area, pore size and pore distributions for the application of an anode material of dye-sensitized solar cells (DSSC), size-controlled and well-dispersed TiO2 nanopowders were synthesized by chemical vapor condensation (CVC) process in the range of 800-1000 degreesC under a pressure of 50 mbar. The average particle size of synthesized TiO2 nanopowders was increased with increasing temperature from 13 nm for 800 degreesC, 15 nm for 900 degreesC and 26 nm. The specific surface area of synthesized nanoparticles were measured as 119.1 m2/g for 800 degreesC, 104.7 m2/g for 900 degreesC and 59.5 m2/g for 1000 degreesC, respectively. The conversion efficiency values (eta%) of DSSC with the synthesized TiO2 nanopowders at 800 degreesC, 900 degreesC, and 1000 degreesC were 2.59%, 5.96% and 3.66%, respectively. The highest conversion efficiency obtained in the 900 degreesC (5.96%) sample is thought to be attributable to homogeneous particle size and pore distributions, large specific surface area, and high transmittance in regions of dye absorption wavelength. PMID:23901483