Silver nanoparticle (AgNP) was synthesized using the cell free extract of Scenedesmus abundans with AgNO3. The synthesized silver nanoparticles were characterized by UV-visible spectroscopy, dynamic light scattering (DLS), scanning electron microscopy (SEM), and Photoluminescence. Bioreduction of Ag
{"title":"Biogenic Synthesis of Silver Nanoparticles Using Scenedesmus abundans and Evaluation of Their Antibacterial Activity","authors":"N. Aziz, T. Fatma, A. Varma, R. Prasad","doi":"10.1155/2014/689419","DOIUrl":"https://doi.org/10.1155/2014/689419","url":null,"abstract":"Silver nanoparticle (AgNP) was synthesized using the cell free extract of Scenedesmus abundans with AgNO3. The synthesized silver nanoparticles were characterized by UV-visible spectroscopy, dynamic light scattering (DLS), scanning electron microscopy (SEM), and Photoluminescence. Bioreduction of Ag","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"2014 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2014-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82142437","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The stability of gold nanoparticles is a major issue which decides their impending usage in nanobiotechnological applications. Often biomimetically synthesized nanoparticles are deemed useless owing to their instability in aqueous medium. So, surfactants are used to stabilize the nanoparticles. But does the surfactant only stabilize by being adsorbed to the surface of the nanoparticles and not play significantly in moulding the size and shape of the nanoparticles? Keeping this idea in mind, gold nanoparticles (GNPs) synthesized by l-tryptophan (Trp) mediated reduction of chloroauric acid (HAuCl4) were stabilized by anionic surfactant, sodium dodecyl sulphate (SDS), and its effect on the moulding of size and properties of the GNPs was studied. Interestingly, unlike most of the gold nanoparticles synthesis mechanism showing saturation growth mechanism, inclusion of SDS in the reaction mixture for GNPs synthesis resulted in a bimodal mechanism which was studied by UV-Vis spectroscopy. The mechanism was further substantiated with transmission electron microscopy. Zeta potential of GNPs solutions was measured to corroborate stability observations recorded visually.
{"title":"Role of Surfactant in the Formation of Gold Nanoparticles in Aqueous Medium","authors":"Abhishek Das, Ridhima Chadha, N. Maiti, S. Kapoor","doi":"10.1155/2014/916429","DOIUrl":"https://doi.org/10.1155/2014/916429","url":null,"abstract":"The stability of gold nanoparticles is a major issue which decides their impending usage in nanobiotechnological applications. Often biomimetically synthesized nanoparticles are deemed useless owing to their instability in aqueous medium. So, surfactants are used to stabilize the nanoparticles. But does the surfactant only stabilize by being adsorbed to the surface of the nanoparticles and not play significantly in moulding the size and shape of the nanoparticles? Keeping this idea in mind, gold nanoparticles (GNPs) synthesized by l-tryptophan (Trp) mediated reduction of chloroauric acid (HAuCl4) were stabilized by anionic surfactant, sodium dodecyl sulphate (SDS), and its effect on the moulding of size and properties of the GNPs was studied. Interestingly, unlike most of the gold nanoparticles synthesis mechanism showing saturation growth mechanism, inclusion of SDS in the reaction mixture for GNPs synthesis resulted in a bimodal mechanism which was studied by UV-Vis spectroscopy. The mechanism was further substantiated with transmission electron microscopy. Zeta potential of GNPs solutions was measured to corroborate stability observations recorded visually.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"21 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90042224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Solid supported 2D assembly of silver nanocubes was fabricated by Langmuir-Blodgett technique and employed to investigate its surface enhanced Raman scattering (SERS) and surface enhance fluorescence (SEF) activities by detecting Rh6G in solution of varied concentrations, that is, 10−12 M, 10−9 M, 10−6 M, and 10−3 M. SERS was detected from a nanomolar concentration of Rh6G whereas SEF was detected from a picomolar concentration. Further, the substrate was subjected to thermal annealing to fabricate plasmonic thin film. The formation of thin film was followed by monitoring its surface plasmon resonance spectra and atomic force microscopic images. It was observed that the characteristic spectral peaks of silver nanocubes merged into a broad spectral band as the annealing time was increased and the intensity of the band decreased with the formation of thin film. The obtained result implies that thermal annealing could be a simple approach to create nanoscale gaps in SERS substrate and to engineer continuous thin film from the assembly of discrete nanoparticles.
采用Langmuir-Blodgett技术制备了固体支撑的二维银纳米立方体组装体，并通过检测不同浓度(10−12 M, 10−9 M, 10−6 M和10−3 M)溶液中的Rh6G，研究了其表面增强拉曼散射(SERS)和表面增强荧光(SEF)活性。SERS从纳摩尔浓度的Rh6G检测，而SEF从皮摩尔浓度检测。此外，对衬底进行热退火以制备等离子体薄膜。薄膜形成后，监测其表面等离子体共振光谱和原子力显微图像。观察到，随着退火时间的延长，银纳米立方体的特征光谱峰合并成一个宽的谱带，而谱带的强度随着薄膜的形成而降低。所得结果表明，热退火可以是在SERS衬底上产生纳米级间隙的一种简单方法，并且可以通过离散纳米颗粒的组装来设计连续薄膜。
{"title":"A Simple Approach to Engineer SERS Substrates and Plasmonic Thin Film","authors":"N. Ahamad, Md Al-Amin, A. Ianoul","doi":"10.1155/2014/602385","DOIUrl":"https://doi.org/10.1155/2014/602385","url":null,"abstract":"Solid supported 2D assembly of silver nanocubes was fabricated by Langmuir-Blodgett technique and employed to investigate its surface enhanced Raman scattering (SERS) and surface enhance fluorescence (SEF) activities by detecting Rh6G in solution of varied concentrations, that is, 10−12 M, 10−9 M, 10−6 M, and 10−3 M. SERS was detected from a nanomolar concentration of Rh6G whereas SEF was detected from a picomolar concentration. Further, the substrate was subjected to thermal annealing to fabricate plasmonic thin film. The formation of thin film was followed by monitoring its surface plasmon resonance spectra and atomic force microscopic images. It was observed that the characteristic spectral peaks of silver nanocubes merged into a broad spectral band as the annealing time was increased and the intensity of the band decreased with the formation of thin film. The obtained result implies that thermal annealing could be a simple approach to create nanoscale gaps in SERS substrate and to engineer continuous thin film from the assembly of discrete nanoparticles.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"194 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2014-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73909559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Synthesis of metallic nanoparticles by chemical and physical method makes the process often cumbersome due the usage of toxic and expensive chemicals. The present study reports the biosynthesis of silver nanoparticles using marine invertebrate (polychaete) extract at room temperature. The ultraviolet-visible (UV-Vis) spectroscopy revealed the formation of silver nanoparticles (AgNPs) by exhibiting the typical surface plasmon absorption maximum at 418–420 nm. Structure and composition of AgNPs were analyzed by atomic force microscopy (AFM). Average particle size of AgNPs ranged from 40 to 90 nm, confirmed by scanning electron microscopy (SEM) analysis. The energy-dispersive X-ray spectroscopy (EDX) of the nanoparticles dispersion confirmed the presence of elemental silver signal, whereas X-ray diffraction (XRD) substantiated the crystalline nature of synthesized nanoparticle. Fourier transform infrared spectroscopy (FTIR) spectral analysis showed the presence of amides phenols, ethers, and fatty acids as major biomolecules responsible for the reduction of silver ions. The possible mechanism responsible for the synthesis of AgNPs by these biomolecules was also illustrated by chemical reactions. The synthesized AgNPs showed comparatively good antibacterial activity against the tested human pathogens. This study advocates that not only plants and microbes but also marine invertebrates do have potential for synthesizing nanoparticles by a cost-effective and eco-friendly approach.
{"title":"Biosynthesis of Silver Nanoparticles by Marine Invertebrate (Polychaete) and Assessment of Its Efficacy against Human Pathogens","authors":"Reena Singh, S. Sahu, M. Thangaraj","doi":"10.1155/2014/718240","DOIUrl":"https://doi.org/10.1155/2014/718240","url":null,"abstract":"Synthesis of metallic nanoparticles by chemical and physical method makes the process often cumbersome due the usage of toxic and expensive chemicals. The present study reports the biosynthesis of silver nanoparticles using marine invertebrate (polychaete) extract at room temperature. The ultraviolet-visible (UV-Vis) spectroscopy revealed the formation of silver nanoparticles (AgNPs) by exhibiting the typical surface plasmon absorption maximum at 418–420 nm. Structure and composition of AgNPs were analyzed by atomic force microscopy (AFM). Average particle size of AgNPs ranged from 40 to 90 nm, confirmed by scanning electron microscopy (SEM) analysis. The energy-dispersive X-ray spectroscopy (EDX) of the nanoparticles dispersion confirmed the presence of elemental silver signal, whereas X-ray diffraction (XRD) substantiated the crystalline nature of synthesized nanoparticle. Fourier transform infrared spectroscopy (FTIR) spectral analysis showed the presence of amides phenols, ethers, and fatty acids as major biomolecules responsible for the reduction of silver ions. The possible mechanism responsible for the synthesis of AgNPs by these biomolecules was also illustrated by chemical reactions. The synthesized AgNPs showed comparatively good antibacterial activity against the tested human pathogens. This study advocates that not only plants and microbes but also marine invertebrates do have potential for synthesizing nanoparticles by a cost-effective and eco-friendly approach.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"164 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88708427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
L. Bubnovskaya, A. Belous, S. Solopan, A. Kovelskaya, L. Bovkun, A. Podoltsev, Igor Kondtratenko, S. Osinsky
Purpose. To test the antitumor activity of magnetic fluid (MF) on the basis of substituted lanthanum-strontium manganite nanoparticles combined with alternating magnetic field (AMF) in experiments with transplanted tumors. Materials and Methods. MF with a size of nanoparticles of 30–40 nm in aqueous agarose solution was investigated. The ability of MF to heat tumor under AMF (300 kHz, 7.7 kA/m) was tested in vivo with rodent tumors (Guerin carcinoma, Walker-256 carcinosarcoma, and Lewis lung carcinoma (3LL)). Results. Single administration of MF into the tumor at a dose of 150 mg/kg (rats) or 200 mg/kg (mice) followed by AMF within 20–30 min (treatment was repeated 3-4-fold) has resulted in the complete regression of tumor in the 35% of rats and 57% of mice. Administration of MF alone or action of AMF alone has not resulted in tumor growth inhibition. The chemomodifying effect of nanohyperthermia was determined, in particular for cisplatinum: thermal enhancement ratio was 2.0. It was also observed that nanohyperthermia has resulted in the absence of 3LL metastases in 43% of mice. Conclusions. MF on the basis of lanthanum-strontium manganite may be considered as an effective inductor of tumor local hyperthermia.
{"title":"Magnetic Fluid Hyperthermia of Rodent Tumors Using Manganese Perovskite Nanoparticles","authors":"L. Bubnovskaya, A. Belous, S. Solopan, A. Kovelskaya, L. Bovkun, A. Podoltsev, Igor Kondtratenko, S. Osinsky","doi":"10.1155/2014/278761","DOIUrl":"https://doi.org/10.1155/2014/278761","url":null,"abstract":"Purpose. To test the antitumor activity of magnetic fluid (MF) on the basis of substituted lanthanum-strontium manganite nanoparticles combined with alternating magnetic field (AMF) in experiments with transplanted tumors. Materials and Methods. MF with a size of nanoparticles of 30–40 nm in aqueous agarose solution was investigated. The ability of MF to heat tumor under AMF (300 kHz, 7.7 kA/m) was tested in vivo with rodent tumors (Guerin carcinoma, Walker-256 carcinosarcoma, and Lewis lung carcinoma (3LL)). Results. Single administration of MF into the tumor at a dose of 150 mg/kg (rats) or 200 mg/kg (mice) followed by AMF within 20–30 min (treatment was repeated 3-4-fold) has resulted in the complete regression of tumor in the 35% of rats and 57% of mice. Administration of MF alone or action of AMF alone has not resulted in tumor growth inhibition. The chemomodifying effect of nanohyperthermia was determined, in particular for cisplatinum: thermal enhancement ratio was 2.0. It was also observed that nanohyperthermia has resulted in the absence of 3LL metastases in 43% of mice. Conclusions. MF on the basis of lanthanum-strontium manganite may be considered as an effective inductor of tumor local hyperthermia.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"64 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2014-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82724677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Electrospraying (electrohydrodynamic spraying) is a method of liquid atomization by electrical forces. Spraying solutions or suspensions allow production of fine particles, down to nanometer size. These particles are interesting for a wide variety of applications, thanks to their unprecedented chemical and physical behaviour in comparison to their bulk form. Knowledge of the particle size in powders is important in many studies employing nanoparticles. In this paper, the effect of some process parameters on the size of electrosprayed polyacrylonitrile particles is presented in the form of response surface model. The model is achieved by employing a factorial design to evaluate the influence of parameters on the polyacrylonitrile nanoparticle size and response surface methodology. Four electrospraying parameters, namely, applied voltage, electrospraying solution concentration, flow rate, and syringe needle diameter were considered.
{"title":"Response Surface Modelling of Electrosprayed Polyacrylonitrile Nanoparticle Size","authors":"Sanaz Khademolqorani, A. Z. Hamadani, H. Tavanai","doi":"10.1155/2014/146218","DOIUrl":"https://doi.org/10.1155/2014/146218","url":null,"abstract":"Electrospraying (electrohydrodynamic spraying) is a method of liquid atomization by electrical forces. Spraying solutions or suspensions allow production of fine particles, down to nanometer size. These particles are interesting for a wide variety of applications, thanks to their unprecedented chemical and physical behaviour in comparison to their bulk form. Knowledge of the particle size in powders is important in many studies employing nanoparticles. In this paper, the effect of some process parameters on the size of electrosprayed polyacrylonitrile particles is presented in the form of response surface model. The model is achieved by employing a factorial design to evaluate the influence of parameters on the polyacrylonitrile nanoparticle size and response surface methodology. Four electrospraying parameters, namely, applied voltage, electrospraying solution concentration, flow rate, and syringe needle diameter were considered.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"83 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84029398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nilesh K. Mahale, R. D. Ladhe, S. Attarde, S. Ingle
We report the synthesis and structural transformation of fcc to hcp in Ni-graphene (Ni-Gr) composite by simple chemical route via sonication. The syntheses of Ni-Gr composite by simultaneous reduction method, and the effect of different composition ratio on morphology and crystal structure were examined in our present study. The results indicated that the graphene ratio played an important role in crystal structure and d-spacing in nickel crystals. Different compositions have shown different behavior. The nanonickel clusters of various shapes with coated graphene and decorated as nickel on graphene sheets are observed. The synthesized composites were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and transmission electron microscope (TEM). The XRD patterns indicated crystal lattice modifications in some composites while composites with a higher graphene ratio produced very small crystals with uniform lattice parameter and d-spacing. FE-SEM images indicated the growth of Datura fruit like shapes of nickel clusters in higher composition of nickel while the composites with least concentration of nickel were composed of cubical nanoparticles grown on graphene sheets. TEM analysis revealed many Ni nanoparticles surrounding the smooth petals like surface of graphene, with average diameters of spiky nickel nanoparticles being about 50 nm and 124 nm, respectively, on 200 nm of scale.
{"title":"Synthesis and the Structural Transformation of fcc to hcp in Ni-Graphene Nanocomposite by Simple Chemical Route via Sonication","authors":"Nilesh K. Mahale, R. D. Ladhe, S. Attarde, S. Ingle","doi":"10.1155/2014/305637","DOIUrl":"https://doi.org/10.1155/2014/305637","url":null,"abstract":"We report the synthesis and structural transformation of fcc to hcp in Ni-graphene (Ni-Gr) composite by simple chemical route via sonication. The syntheses of Ni-Gr composite by simultaneous reduction method, and the effect of different composition ratio on morphology and crystal structure were examined in our present study. The results indicated that the graphene ratio played an important role in crystal structure and d-spacing in nickel crystals. Different compositions have shown different behavior. The nanonickel clusters of various shapes with coated graphene and decorated as nickel on graphene sheets are observed. The synthesized composites were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and transmission electron microscope (TEM). The XRD patterns indicated crystal lattice modifications in some composites while composites with a higher graphene ratio produced very small crystals with uniform lattice parameter and d-spacing. FE-SEM images indicated the growth of Datura fruit like shapes of nickel clusters in higher composition of nickel while the composites with least concentration of nickel were composed of cubical nanoparticles grown on graphene sheets. TEM analysis revealed many Ni nanoparticles surrounding the smooth petals like surface of graphene, with average diameters of spiky nickel nanoparticles being about 50 nm and 124 nm, respectively, on 200 nm of scale.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"5 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84560907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The results of carbon-doped zinc oxide nanoparticles synthesized by CO2 microwave plasma at atmospheric pressure are presented. The 2.45-GHz microwave plasma torch and feeder for injecting Zn granules are used in the synthesis of zinc oxide nanoparticles. The Zn granules (13.5 g/min) were introduced into the microwave plasma by CO2 (5 l/min) swirl gas. The microwave power delivered to the CO2 microwave plasma was 1 kW. The synthesis of carbon-doped zinc oxide nanoparticles was carried out in accordance with CO2
{"title":"Optical and Structural Properties of ZnO Nanoparticles Synthesized by CO2 Microwave Plasma at Atmospheric Pressure","authors":"Se M. Chun, D. Choi, J. Park, Y. Hong","doi":"10.1155/2014/734256","DOIUrl":"https://doi.org/10.1155/2014/734256","url":null,"abstract":"The results of carbon-doped zinc oxide nanoparticles synthesized by CO2 microwave plasma at atmospheric pressure are presented. The 2.45-GHz microwave plasma torch and feeder for injecting Zn granules are used in the synthesis of zinc oxide nanoparticles. The Zn granules (13.5 g/min) were introduced into the microwave plasma by CO2 (5 l/min) swirl gas. The microwave power delivered to the CO2 microwave plasma was 1 kW. The synthesis of carbon-doped zinc oxide nanoparticles was carried out in accordance with CO2","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"42 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73946077","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nanomaterials exhibit unique physical and chemical properties and, hence, they have received much attention from scientists and researchers in different areas of environmental sciences, specifically in bioremediation. Bioremediation provides a good clean-up strategy for some types of waste, but as it is expected, it will not be useful for all. For example, bioremediation may not provide a feasible strategy at sites with high concentrations of chemicals that are toxic to most microorganisms. These include heavy metals and salt. Further, the advancement in science and technology has increased standard of living which directly or indirectly contributes to the increase in waste and toxic material. Therefore, the remediation of contaminants by use of existing technology is not effective and efficient in cleaning up the environment. Hence, nanomaterials may be applied for bioremediation, which will not only have less toxic effect on microorganisms, but will also improve the microbial activity of the specific waste and toxic material which will reduce the overall time consumption as well as reduce the overall cost. In this paper we have briefly summarized the major types of nanomaterials that have been used so far in bioremediation of waste and toxic materials.
{"title":"Ecofriendly Application of Nanomaterials: Nanobioremediation","authors":"Rizwan, Man Singh, C. Mitra, Roshan K. Morve","doi":"10.1155/2014/431787","DOIUrl":"https://doi.org/10.1155/2014/431787","url":null,"abstract":"Nanomaterials exhibit unique physical and chemical properties and, hence, they have received much attention from scientists and researchers in different areas of environmental sciences, specifically in bioremediation. Bioremediation provides a good clean-up strategy for some types of waste, but as it is expected, it will not be useful for all. For example, bioremediation may not provide a feasible strategy at sites with high concentrations of chemicals that are toxic to most microorganisms. These include heavy metals and salt. Further, the advancement in science and technology has increased standard of living which directly or indirectly contributes to the increase in waste and toxic material. Therefore, the remediation of contaminants by use of existing technology is not effective and efficient in cleaning up the environment. Hence, nanomaterials may be applied for bioremediation, which will not only have less toxic effect on microorganisms, but will also improve the microbial activity of the specific waste and toxic material which will reduce the overall time consumption as well as reduce the overall cost. In this paper we have briefly summarized the major types of nanomaterials that have been used so far in bioremediation of waste and toxic materials.","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"55 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2014-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84900546","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Iron nanoparticles are synthesized and size characterized using HRTEM, FESEM, and XRD. Polyethylene glycol(PEG), carboxymethyl cellulose (CMC), and poly N-vinyl pyrrolidone (PVP) are used as nanoparticle stabilizers. The sizes of Fe nps are found to be 9 nm, 14 nm, and 17 nm ± 1 nm corresponding to PEG, CMC, and PVP stabilizers, respectively. The three different iron nanoparticles (Fe nps) prepared are used as catalysts in the hydrogenation reaction of various substituted aromatic ketones to alcohols with NaBH4. The progress of the reaction was monitored using time variance UV spectra. Kinetic plots are made from the absorbance values and the pseudo first order rate coefficient values are determined. Catalytic efficiency of the Fe nps is obtained by comparing the pseudo first order rate coefficient values, times of reaction, and % yield. Fe-PEG nps was found to act as better catalyst than Fe-CMC nps and Fe-PVP nps. Also, effects of substituents in the aromatic ring of ketones reveal that
{"title":"Studies on the Iron Nanoparticles Catalyzed Reduction of Substituted Aromatic Ketones to Alcohols","authors":"L. Parimala, J. Santhanalakshmi","doi":"10.1155/2014/156868","DOIUrl":"https://doi.org/10.1155/2014/156868","url":null,"abstract":"Iron nanoparticles are synthesized and size characterized using HRTEM, FESEM, and XRD. Polyethylene glycol(PEG), carboxymethyl cellulose (CMC), and poly N-vinyl pyrrolidone (PVP) are used as nanoparticle stabilizers. The sizes of Fe nps are found to be 9 nm, 14 nm, and 17 nm ± 1 nm corresponding to PEG, CMC, and PVP stabilizers, respectively. The three different iron nanoparticles (Fe nps) prepared are used as catalysts in the hydrogenation reaction of various substituted aromatic ketones to alcohols with NaBH4. The progress of the reaction was monitored using time variance UV spectra. Kinetic plots are made from the absorbance values and the pseudo first order rate coefficient values are determined. Catalytic efficiency of the Fe nps is obtained by comparing the pseudo first order rate coefficient values, times of reaction, and % yield. Fe-PEG nps was found to act as better catalyst than Fe-CMC nps and Fe-PVP nps. Also, effects of substituents in the aromatic ring of ketones reveal that","PeriodicalId":16507,"journal":{"name":"Journal of Nanoparticles","volume":"6 1","pages":"1-10"},"PeriodicalIF":0.0,"publicationDate":"2014-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89034895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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