Bernard Otieno Sadia, J. Cherutoi, Cleophas Mecha Achisa
The economic burden and high mortality associated with multidrug-resistant bacteria is a major public health concern. Biosynthesized copper nanoparticles (CuNPs) could be a potential alternative to combat bacterial resistance to conventional medicine. This study for the first time aimed at optimizing the synthesis conditions (concentration of copper ions, temperature, and pH) to obtain the smallest size of CuNPs, characterizing and testing the antibacterial efficacy of CuNPs prepared from Senna didymobotrya (S. didymobotrya) roots. Extraction was done by the Soxhlet method using methanol as the solvent. Gas chromatography-mass spectrometry (GC-MS) analysis was performed to identify compounds in S. didymobotrya root extracts. Box–Behnken design was used to obtain optimal synthesis conditions as determined using a particle analyzer. Characterization was done using ultraviolet-visible (UV-Vis), particle size analyzer, X-ray diffraction, zeta potentiometer, and Fourier transform infrared (FT-IR). Bioassay was conducted using the Kirby–Bauer disk diffusion susceptibility test. The major compounds identified by GC-MS in reference to the NIST library were benzoic acid, thymol, N-benzyl-2-phenethylamine, benzaldehyde, vanillin, phenylacetic acid, and benzothiazole. UV-Vis spectrum showed a characteristic peak at 570 nm indicating the formation of CuNPs. The optimum synthesis conditions were temperature of 80°C, pH 3.0, and copper ion concentration of 0.0125 M. The FT-IR spectrum showed absorptions in the range 3500–3400 cm−1 (N-H stretch), 3400–2400 cm−1 (O-H stretch), and 988–830 cm−1 (C-H bend) and peak at 1612 cm−1 (C=C stretch), and 1271 cm−1 (C-O bend). Cu nanoparticle sizes were 5.55–63.60 nm. The zeta potential value was −69.4 mV indicating that they were stable. The biosynthesized nanoparticles exhibited significant antimicrobial activity on Escherichia coli and Staphylococcus aureus with the zone of inhibition diameters of 26.00 ± 0.58 mm and 30.00 ± 0.58 mm compared to amoxicillin clavulanate (standard) with inhibition diameters of 20 ± 0.58 mm and 28.00 ± 0.58 mm, respectively.
{"title":"Optimization, Characterization, and Antibacterial Activity of Copper Nanoparticles Synthesized Using Senna didymobotrya Root Extract","authors":"Bernard Otieno Sadia, J. Cherutoi, Cleophas Mecha Achisa","doi":"10.1155/2021/5611434","DOIUrl":"https://doi.org/10.1155/2021/5611434","url":null,"abstract":"The economic burden and high mortality associated with multidrug-resistant bacteria is a major public health concern. Biosynthesized copper nanoparticles (CuNPs) could be a potential alternative to combat bacterial resistance to conventional medicine. This study for the first time aimed at optimizing the synthesis conditions (concentration of copper ions, temperature, and pH) to obtain the smallest size of CuNPs, characterizing and testing the antibacterial efficacy of CuNPs prepared from Senna didymobotrya (S. didymobotrya) roots. Extraction was done by the Soxhlet method using methanol as the solvent. Gas chromatography-mass spectrometry (GC-MS) analysis was performed to identify compounds in S. didymobotrya root extracts. Box–Behnken design was used to obtain optimal synthesis conditions as determined using a particle analyzer. Characterization was done using ultraviolet-visible (UV-Vis), particle size analyzer, X-ray diffraction, zeta potentiometer, and Fourier transform infrared (FT-IR). Bioassay was conducted using the Kirby–Bauer disk diffusion susceptibility test. The major compounds identified by GC-MS in reference to the NIST library were benzoic acid, thymol, N-benzyl-2-phenethylamine, benzaldehyde, vanillin, phenylacetic acid, and benzothiazole. UV-Vis spectrum showed a characteristic peak at 570 nm indicating the formation of CuNPs. The optimum synthesis conditions were temperature of 80°C, pH 3.0, and copper ion concentration of 0.0125 M. The FT-IR spectrum showed absorptions in the range 3500–3400 cm−1 (N-H stretch), 3400–2400 cm−1 (O-H stretch), and 988–830 cm−1 (C-H bend) and peak at 1612 cm−1 (C=C stretch), and 1271 cm−1 (C-O bend). Cu nanoparticle sizes were 5.55–63.60 nm. The zeta potential value was −69.4 mV indicating that they were stable. The biosynthesized nanoparticles exhibited significant antimicrobial activity on Escherichia coli and Staphylococcus aureus with the zone of inhibition diameters of 26.00 ± 0.58 mm and 30.00 ± 0.58 mm compared to amoxicillin clavulanate (standard) with inhibition diameters of 20 ± 0.58 mm and 28.00 ± 0.58 mm, respectively.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"68 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2021-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72645930","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}
Toga Khalid Mohamed, Marivt Osman Widdatallah, Maida Musa Ali, Afraa Mubarak Alhaj, DhiaEldin AbdElmagied Elhag
An extremely worrying and alarming increase in the level of multiple drug resistance is reported in Sudan, in which bacterial strains are becoming resistant to many commonly available antibiotics. Eventually, it is becoming extremely difficult to treat debilitating infections. In search of promising solutions to this arising crisis, Camellia sinensis silver nanoparticles were synthesized using the green synthesis method. The synthesis of the Camellia sinensis silver nanoparticles is confirmed using analytical methods as ultraviolet-visible spectroscopy, X-ray diffractometer, and scanning electron microscopy. Using the ultraviolet-visible spectroscopy, an absorption band of 412 nm was observed. Furthermore, scanning electron microscopy revealed the presence of silver nanoparticles which fell within the range of 1–100 nm, and X-ray diffractometer analysis showed three intense peaks with a maximum intense peak at 24.3 theta. Nanoparticles distribution between 12 nm and 64 nm was observed with an average diameter of 18.115 nm. It also revealed orthorhombic-shaped nanoparticles. The synthesized nanoparticles showed antimicrobial activity against Staphylococcus aureus with a zone of inhibition of 7 mm, but none was detected against Escherichia coli. The obtained physicochemical properties were correlated with the antibacterial activity of the silver nanoparticles.
{"title":"Green Synthesis, Characterization, and Evaluation of the Antimicrobial Activity of Camellia sinensis Silver Nanoparticles","authors":"Toga Khalid Mohamed, Marivt Osman Widdatallah, Maida Musa Ali, Afraa Mubarak Alhaj, DhiaEldin AbdElmagied Elhag","doi":"10.1155/2021/2867404","DOIUrl":"https://doi.org/10.1155/2021/2867404","url":null,"abstract":"An extremely worrying and alarming increase in the level of multiple drug resistance is reported in Sudan, in which bacterial strains are becoming resistant to many commonly available antibiotics. Eventually, it is becoming extremely difficult to treat debilitating infections. In search of promising solutions to this arising crisis, Camellia sinensis silver nanoparticles were synthesized using the green synthesis method. The synthesis of the Camellia sinensis silver nanoparticles is confirmed using analytical methods as ultraviolet-visible spectroscopy, X-ray diffractometer, and scanning electron microscopy. Using the ultraviolet-visible spectroscopy, an absorption band of 412 nm was observed. Furthermore, scanning electron microscopy revealed the presence of silver nanoparticles which fell within the range of 1–100 nm, and X-ray diffractometer analysis showed three intense peaks with a maximum intense peak at 24.3 theta. Nanoparticles distribution between 12 nm and 64 nm was observed with an average diameter of 18.115 nm. It also revealed orthorhombic-shaped nanoparticles. The synthesized nanoparticles showed antimicrobial activity against Staphylococcus aureus with a zone of inhibition of 7 mm, but none was detected against Escherichia coli. The obtained physicochemical properties were correlated with the antibacterial activity of the silver nanoparticles.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"21 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87570693","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}
ZnO/Si heterojunctions have been fabricated by spinning ZnO nanoflakes on the p-type single crystal silicon by using the spin coating technique. Photoluminescence spectra of as-grown and annealed ZnO/Si heterojunctions have been recorded under the excitation of 336 nm. Multipeaks between ∼360 nm and ∼430 nm from annealed ZnO/Si heterojunctions have been analyzed, the origins of which have been ascribed to the effects of one or multiple LO phonons. The rectifying effects can be observed from the prototypical devices based on ZnO/Si heterojunctions. Although the parameters obtained by analyzing the current density-voltage characteristics are away from those from the ideal device, it is believed that ZnO/Si heterojunctions in the present work will be a potential candidate in the optoelectronic field through modulating and optimizing the fabrication conditions.
{"title":"Multipeak Emissions and Electrical Properties of ZnO/Si Heterojunctions Based on ZnO Nanoflakes by Spin Coating Technique","authors":"Yalan Ma, P. Ji, Yong Li, Yueli Song","doi":"10.1155/2021/9267962","DOIUrl":"https://doi.org/10.1155/2021/9267962","url":null,"abstract":"ZnO/Si heterojunctions have been fabricated by spinning ZnO nanoflakes on the p-type single crystal silicon by using the spin coating technique. Photoluminescence spectra of as-grown and annealed ZnO/Si heterojunctions have been recorded under the excitation of 336 nm. Multipeaks between ∼360 nm and ∼430 nm from annealed ZnO/Si heterojunctions have been analyzed, the origins of which have been ascribed to the effects of one or multiple LO phonons. The rectifying effects can be observed from the prototypical devices based on ZnO/Si heterojunctions. Although the parameters obtained by analyzing the current density-voltage characteristics are away from those from the ideal device, it is believed that ZnO/Si heterojunctions in the present work will be a potential candidate in the optoelectronic field through modulating and optimizing the fabrication conditions.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"58 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2021-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84124659","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}
P. Pisitsak, Kwandee Chamchoy, Varanrada Chinprateep, Wiphawan Khobthong, Pisutsaran Chitichotpanya, S. Ummartyotin
Gold nanoparticles (AuNPs) were synthesized under ambient conditions from chloroauric acid in aqueous solution at pH 4. Tannin-rich extract from Xylocarpus granatum bark was used as both reducing and capping agent, rapidly converting Au (I) salt to AuNPs. Transmission electron microscopy showed the as-prepared AuNPs to be predominantly spherical, with an average diameter of 17 nm. The AuNPs were tested for catalytic reduction of Congo red (CR), a carcinogenic azo dye, in aqueous sodium borohydride solution. Cotton samples were coated with the AuNPs, taking on a reddish-purple color. The samples showed significantly reduced tearing strength after coating, though tensile strength was unaffected. UV-visible spectroscopy was used to determine the dye concentration in the water. CR degradation was observed only when AuNPs were present, and the efficiency of degradation was strongly linked to the AuNP loading. The AuNP-coated fabrics left only a 4.7% CR concentration in the solution after 24 h and therefore promise as a heterogeneous catalyst for degradation of CR in aqueous solution.
{"title":"Synthesis of Gold Nanoparticles Using Tannin-Rich Extract and Coating onto Cotton Textiles for Catalytic Degradation of Congo Red","authors":"P. Pisitsak, Kwandee Chamchoy, Varanrada Chinprateep, Wiphawan Khobthong, Pisutsaran Chitichotpanya, S. Ummartyotin","doi":"10.1155/2021/6380283","DOIUrl":"https://doi.org/10.1155/2021/6380283","url":null,"abstract":"Gold nanoparticles (AuNPs) were synthesized under ambient conditions from chloroauric acid in aqueous solution at pH 4. Tannin-rich extract from Xylocarpus granatum bark was used as both reducing and capping agent, rapidly converting Au (I) salt to AuNPs. Transmission electron microscopy showed the as-prepared AuNPs to be predominantly spherical, with an average diameter of 17 nm. The AuNPs were tested for catalytic reduction of Congo red (CR), a carcinogenic azo dye, in aqueous sodium borohydride solution. Cotton samples were coated with the AuNPs, taking on a reddish-purple color. The samples showed significantly reduced tearing strength after coating, though tensile strength was unaffected. UV-visible spectroscopy was used to determine the dye concentration in the water. CR degradation was observed only when AuNPs were present, and the efficiency of degradation was strongly linked to the AuNP loading. The AuNP-coated fabrics left only a 4.7% CR concentration in the solution after 24 h and therefore promise as a heterogeneous catalyst for degradation of CR in aqueous solution.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"53 7 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2021-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86781476","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. Chotirat, S. Niyomwas, Witthawat Wongpisan, S. Supothina
The vanadium dioxide (VO2) thin films were synthesized by sol-gel dipping on a glass slide substrate at low temperature of 500°C in a vacuum tube furnace at a pressure of 2 × 10−3 mbar by 2-step calcination without an intermediate gas purging. Synthesis conditions, including temperature, vacuum pressure, and calcination steps in the vacuum tube furnace, were investigated to find the optimum condition that promoted the formation of VO2 phase. It was found that the 2nd calcination step was very important in realizing the monoclinic vanadium dioxide (VO2 (M)). The results of the valence electron analysis revealed the outstanding phase of VO2 and a small amount of V2O5 and V2O3 phases. The small crystallites of the VO2 were homogeneously distributed on the surface, and the grain was of an irregular shape of ∼220−380 nm in size. The film’s thickness was in a range of 69−74 nm. The film exhibited a metal-to-insulator transformation temperature of ∼68oC and good thermochromic property. Visible optical transmittance remained at ∼40−50% when the sample’s temperature changed from 25 to 80°C for a near infrared (NIR) region.
{"title":"Low-Temperature Synthesis of Vanadium Dioxide Thin Films by Sol-Gel Dip Coating Method","authors":"L. Chotirat, S. Niyomwas, Witthawat Wongpisan, S. Supothina","doi":"10.1155/2021/4868152","DOIUrl":"https://doi.org/10.1155/2021/4868152","url":null,"abstract":"The vanadium dioxide (VO2) thin films were synthesized by sol-gel dipping on a glass slide substrate at low temperature of 500°C in a vacuum tube furnace at a pressure of 2 × 10−3 mbar by 2-step calcination without an intermediate gas purging. Synthesis conditions, including temperature, vacuum pressure, and calcination steps in the vacuum tube furnace, were investigated to find the optimum condition that promoted the formation of VO2 phase. It was found that the 2nd calcination step was very important in realizing the monoclinic vanadium dioxide (VO2 (M)). The results of the valence electron analysis revealed the outstanding phase of VO2 and a small amount of V2O5 and V2O3 phases. The small crystallites of the VO2 were homogeneously distributed on the surface, and the grain was of an irregular shape of ∼220−380 nm in size. The film’s thickness was in a range of 69−74 nm. The film exhibited a metal-to-insulator transformation temperature of ∼68oC and good thermochromic property. Visible optical transmittance remained at ∼40−50% when the sample’s temperature changed from 25 to 80°C for a near infrared (NIR) region.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"49 1","pages":"1-7"},"PeriodicalIF":4.2,"publicationDate":"2021-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83660427","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 present study describes the antioxidant, antimicrobial, and photocatalytic activity of silver nanoparticles (AGNPs) synthesized using six varieties of Catharanthus roseus flower extracts for the first time. Initially, the synthesized AgNPs were visually confirmed by color change. Further, the formation, size, and shape of the synthesized AgNPs were characterized by UV-Vis spectroscopy and scanning electron microscopy (SEM). The SEM image of purple flower AgNPs and the calculated bandgap energies of the synthesized AgNPs showed that the synthesized AgNPs were in the range of 0–30 nm. Qualitative phytochemical analysis revealed the presence of the phytocompounds that were responsible for the capping, formation, bioreduction, and stabilization of AgNPs. The antioxidant ability of the AgNPs and their respective flower extracts were analyzed using TFC, TPC, TAC, DPPH, FRAP, and IC50 assays. The results of the antioxidant assays indicated that the AgNPs showed higher antioxidant activity compared to their respective flower extracts. The synthesized AgNPs showed significant antimicrobial activity against Gram-negative Escherichia coli compared to Gram-positive Staphylococcus aureus assayed using the agar well diffusion method. Furthermore, the photocatalytic activity of the synthesized purple flower AgNPs at two different concentrations 5000 ppm and 333 ppm was analyzed by the removal of methyl orange dye from an aqueous solution under sunlight irradiation in the presence of NaBH4 catalyst. Results indicated that 333 ppm purple flower AgNPs exhibited an efficient photocatalytic activity in the degradation of methyl orange compared to 5000 ppm purple flower AgNPs in 20 minutes. Thus, the results obtained indicated that Catharanthus roseus is an ecofriendly source for the green synthesis of AgNPs which can be used as a novel antioxidant, antimicrobial, and photocatalytic agent; thereby, it can be used in a variety of applications to improve the quality of human life.
{"title":"Green Synthesis of Silver Nanoparticles Using Catharanthus roseus Flower Extracts and the Determination of Their Antioxidant, Antimicrobial, and Photocatalytic Activity","authors":"M. Kandiah, Kavishadhi N. Chandrasekaran","doi":"10.1155/2021/5512786","DOIUrl":"https://doi.org/10.1155/2021/5512786","url":null,"abstract":"The present study describes the antioxidant, antimicrobial, and photocatalytic activity of silver nanoparticles (AGNPs) synthesized using six varieties of Catharanthus roseus flower extracts for the first time. Initially, the synthesized AgNPs were visually confirmed by color change. Further, the formation, size, and shape of the synthesized AgNPs were characterized by UV-Vis spectroscopy and scanning electron microscopy (SEM). The SEM image of purple flower AgNPs and the calculated bandgap energies of the synthesized AgNPs showed that the synthesized AgNPs were in the range of 0–30 nm. Qualitative phytochemical analysis revealed the presence of the phytocompounds that were responsible for the capping, formation, bioreduction, and stabilization of AgNPs. The antioxidant ability of the AgNPs and their respective flower extracts were analyzed using TFC, TPC, TAC, DPPH, FRAP, and IC50 assays. The results of the antioxidant assays indicated that the AgNPs showed higher antioxidant activity compared to their respective flower extracts. The synthesized AgNPs showed significant antimicrobial activity against Gram-negative Escherichia coli compared to Gram-positive Staphylococcus aureus assayed using the agar well diffusion method. Furthermore, the photocatalytic activity of the synthesized purple flower AgNPs at two different concentrations 5000 ppm and 333 ppm was analyzed by the removal of methyl orange dye from an aqueous solution under sunlight irradiation in the presence of NaBH4 catalyst. Results indicated that 333 ppm purple flower AgNPs exhibited an efficient photocatalytic activity in the degradation of methyl orange compared to 5000 ppm purple flower AgNPs in 20 minutes. Thus, the results obtained indicated that Catharanthus roseus is an ecofriendly source for the green synthesis of AgNPs which can be used as a novel antioxidant, antimicrobial, and photocatalytic agent; thereby, it can be used in a variety of applications to improve the quality of human life.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"82 1","pages":"1-18"},"PeriodicalIF":4.2,"publicationDate":"2021-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83621502","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}
V. N. X. Que, T. T. Khôi, N. Thuy, T. T. Dung, Dao Thi Thanh Binh, N. Huy
The treatment of wastewater from the textile industry containing organic dyes faces many challenges since these compounds resist the biodegradation process in conventional treatment units. Among the physicochemical processes, photocatalysis is considered a facile, cheap, and environmental-friendly technology for treating persistent organic pollutants in waters at low concentrations. This study investigated several physicochemical factors determining the photocatalytic activity of titanate nanotubes (TNTs) to remove Procion MX 032 (PMX), an azo dye, in waters. Degradation of PMX by photocatalytic oxidation process at room temperature (30°C) was set up with the UV irradiation in the presence of different types of photocatalyst such as ST-01 (100% anatase), industrial TiO2, TNTs calcined at 120°C and 500°C. Effect of reaction time, catalyst amount, pH, light wavelength and intensity, and oxidants was investigated. Consequently, TNTs calcined at 500°C provided the highest removal efficiency. The photocatalytic oxidation of PMX by TNT calcined at 500°C was affected by pH variation, getting the highest removal at pH of 8, and inhibited with the presence of H2O2 and O2. Particularly, the PMX degradation using titanate nanotubes was optimized under the UV-A intensity of 100 W/m2. The dye was degraded by more than 95% at the TNTs concentration of 75 mg/L and pH 8.0 after 90 min. The results suggest that photocatalysis using TNTs can be a simple but efficient treatment method to remove PMX and potentially be applied for the treatment of wastewaters containing dyes.
{"title":"Factors Determining the Removal Efficiency of Procion MX in Waters Using Titanate Nanotubes Catalyzed by UV Irradiation","authors":"V. N. X. Que, T. T. Khôi, N. Thuy, T. T. Dung, Dao Thi Thanh Binh, N. Huy","doi":"10.1155/2021/8870453","DOIUrl":"https://doi.org/10.1155/2021/8870453","url":null,"abstract":"The treatment of wastewater from the textile industry containing organic dyes faces many challenges since these compounds resist the biodegradation process in conventional treatment units. Among the physicochemical processes, photocatalysis is considered a facile, cheap, and environmental-friendly technology for treating persistent organic pollutants in waters at low concentrations. This study investigated several physicochemical factors determining the photocatalytic activity of titanate nanotubes (TNTs) to remove Procion MX 032 (PMX), an azo dye, in waters. Degradation of PMX by photocatalytic oxidation process at room temperature (30°C) was set up with the UV irradiation in the presence of different types of photocatalyst such as ST-01 (100% anatase), industrial TiO2, TNTs calcined at 120°C and 500°C. Effect of reaction time, catalyst amount, pH, light wavelength and intensity, and oxidants was investigated. Consequently, TNTs calcined at 500°C provided the highest removal efficiency. The photocatalytic oxidation of PMX by TNT calcined at 500°C was affected by pH variation, getting the highest removal at pH of 8, and inhibited with the presence of H2O2 and O2. Particularly, the PMX degradation using titanate nanotubes was optimized under the UV-A intensity of 100 W/m2. The dye was degraded by more than 95% at the TNTs concentration of 75 mg/L and pH 8.0 after 90 min. The results suggest that photocatalysis using TNTs can be a simple but efficient treatment method to remove PMX and potentially be applied for the treatment of wastewaters containing dyes.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"34 1","pages":"1-10"},"PeriodicalIF":4.2,"publicationDate":"2021-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75983962","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}
Health issues involving inadequate treatment of diseases such as cancer and microbial infections continue to be the subject of much ongoing recent research. Biosynthesized silver nanoparticles (AgNPs) were characterized using Transmission Electron Microscopy (TEM), Zeta Sizer, Ultraviolet (UV), and Fourier Transform Infrared (FTIR) spectroscopy. Their antimicrobial activity was evaluated on selected Gram-positive and Gram-negative bacterial strains, using the disc diffusion and broth dilution assays. Cell viability profiles were evaluated using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and apoptosis studies on selected human noncancer and cancer cells. The biosynthesized AgNPs were evaluated to be spherical clusters, with sizes between 40 and 70 nm. The absorption peak at 423 nm and the presence of polyphenols confirmed the synthesis and stabilization of these tested AgNPs. The AgNPs showed a good stability of −23.9 ± 1.02 mV. Good antimicrobial activity (6.0–18.0 mm) was seen on all tested bacteria at a minimum inhibitory concentration (MIC) ranging from 5 to 16 μg/ml, with the highest activity seen against Gram-negative Escherichia coli (18 ± 0.5 mm), and the lowest activity was seen against Gram-positive Listeria monocytogenes (6.0 ± 0.4 mm) after treatment with the AgNPs. These NPs showed a concentration-dependent and cell-specific cytotoxicity with low IC50 values (41.7, 56.3, and 63.8 μg/ml). The NPs were well tolerated by tested cells as indicated by a more than 50% cell viability at the high dose tested and low apoptotic indices (<0.2). These findings indicated that these biosynthesized AgNPs showed great potential as effective antibacterial agents and anticancer drug delivery modalities.
{"title":"Anticancer and Antimicrobial Activity Evaluation of Cowpea-Porous-Starch-Formulated Silver Nanoparticles","authors":"Shiara Ramdath, J. Mellem, L. Mbatha","doi":"10.1155/2021/5525690","DOIUrl":"https://doi.org/10.1155/2021/5525690","url":null,"abstract":"Health issues involving inadequate treatment of diseases such as cancer and microbial infections continue to be the subject of much ongoing recent research. Biosynthesized silver nanoparticles (AgNPs) were characterized using Transmission Electron Microscopy (TEM), Zeta Sizer, Ultraviolet (UV), and Fourier Transform Infrared (FTIR) spectroscopy. Their antimicrobial activity was evaluated on selected Gram-positive and Gram-negative bacterial strains, using the disc diffusion and broth dilution assays. Cell viability profiles were evaluated using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and apoptosis studies on selected human noncancer and cancer cells. The biosynthesized AgNPs were evaluated to be spherical clusters, with sizes between 40 and 70 nm. The absorption peak at 423 nm and the presence of polyphenols confirmed the synthesis and stabilization of these tested AgNPs. The AgNPs showed a good stability of −23.9 ± 1.02 mV. Good antimicrobial activity (6.0–18.0 mm) was seen on all tested bacteria at a minimum inhibitory concentration (MIC) ranging from 5 to 16 μg/ml, with the highest activity seen against Gram-negative Escherichia coli (18 ± 0.5 mm), and the lowest activity was seen against Gram-positive Listeria monocytogenes (6.0 ± 0.4 mm) after treatment with the AgNPs. These NPs showed a concentration-dependent and cell-specific cytotoxicity with low IC50 values (41.7, 56.3, and 63.8 μg/ml). The NPs were well tolerated by tested cells as indicated by a more than 50% cell viability at the high dose tested and low apoptotic indices (<0.2). These findings indicated that these biosynthesized AgNPs showed great potential as effective antibacterial agents and anticancer drug delivery modalities.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"235 1","pages":"1-13"},"PeriodicalIF":4.2,"publicationDate":"2021-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82861813","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}
Aklilu Guale Bekru, Osman Ahmed Zelekew, D. Andoshe, F. K. Sabir, R. Eswaramoorthy
Copper-oxide-based nanomaterials play an important role as a low-cost alternative to nanoparticles of precious metals for the catalytic reduction of 4-nitrophenols. In this study, CuO nanoparticles were synthesized by a microwave-assisted method using Cordia africana Lam. leaf extract for reduction or stabilization processes. The synthesized CuO nanoparticles (NPs) were characterized using X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS). The analysis indicated that nanocrystals of the monoclinic CuO phase having a cluster of agglomerated morphology with a crystallite size of about 9 nm were synthesized. We also evaluated the catalytic performance of CuO NPs against 4-nitrophenol (4-NP) reduction. The catalyst has shown excellent performance completing the reaction within 12 min. Furthermore, the performance of CuO NPs synthesized at different pH values was investigated, and results indicated that the one synthesized at pH 7 reduced 4-NP effectively in shorter minutes compared to those obtained at higher pH values. The CuO NPs synthesized using Cordia africana Lam. leaf extract exhibited a better reducing capacity with an activity parameter constant of 75.8 min−1·g−1. Thus, CuO synthesized using Cordia africana Lam. holds a potential application for the catalytic conversion of nitroarene compounds into aminoarene.
{"title":"Microwave-Assisted Synthesis of CuO Nanoparticles Using Cordia africana Lam. Leaf Extract for 4-Nitrophenol Reduction","authors":"Aklilu Guale Bekru, Osman Ahmed Zelekew, D. Andoshe, F. K. Sabir, R. Eswaramoorthy","doi":"10.1155/2021/5581621","DOIUrl":"https://doi.org/10.1155/2021/5581621","url":null,"abstract":"Copper-oxide-based nanomaterials play an important role as a low-cost alternative to nanoparticles of precious metals for the catalytic reduction of 4-nitrophenols. In this study, CuO nanoparticles were synthesized by a microwave-assisted method using Cordia africana Lam. leaf extract for reduction or stabilization processes. The synthesized CuO nanoparticles (NPs) were characterized using X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS). The analysis indicated that nanocrystals of the monoclinic CuO phase having a cluster of agglomerated morphology with a crystallite size of about 9 nm were synthesized. We also evaluated the catalytic performance of CuO NPs against 4-nitrophenol (4-NP) reduction. The catalyst has shown excellent performance completing the reaction within 12 min. Furthermore, the performance of CuO NPs synthesized at different pH values was investigated, and results indicated that the one synthesized at pH 7 reduced 4-NP effectively in shorter minutes compared to those obtained at higher pH values. The CuO NPs synthesized using Cordia africana Lam. leaf extract exhibited a better reducing capacity with an activity parameter constant of 75.8 min−1·g−1. Thus, CuO synthesized using Cordia africana Lam. holds a potential application for the catalytic conversion of nitroarene compounds into aminoarene.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"138 1","pages":"1-12"},"PeriodicalIF":4.2,"publicationDate":"2021-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73144402","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}
Antimicrobial activity of copper chalcogenides nanoparticles was investigated by synthesizing copper selenide, copper sulfide, and copper oxide via the hot-injection method. Since reaction time has a profound effect on the nanocrystals size and shapes, the effect of reaction time was also investigated during the synthesis of the copper chalcogenides to obtain nanocrystals with desired properties. The reaction time showed no effect on the phase composition of the synthesized copper sulfide, copper oxide, and copper selenide nanoparticles. However, the size variation of nanoparticles with different reaction time was observed. Reaction time of 30 minutes gave the best optical (the shape of the absorption band edge and emission maxima values) and structural (size distribution of particles) properties for CuSe and CuS compared to other reaction times (15, 45, and 60 min). Their band edges were located at 506 (2.45 eV) and 538 nm (2.30 eV), respectively. For this reaction time, copper selenide produced nanoparticles with a size range of 1–27 nm and copper sulfide nanoparticles ranged 1–18 nm. The morphologies of both chalcogenides at 30 min reaction time were spherical. Reaction time of 15 minutes gave the best optical and structural properties for copper oxide nanoparticles with a band edge of 454 nm (2.73 eV) and particle size ranging 0.8–3.2 nm, but nonetheless, 30 min was used as the optimum reaction time for all three chalcogenides. The optimum parameter (220°C, 30 min, and 1 : 1 ratio) was used to synthesize the three copper chalcogenides which were then tested against Gram-negative (E. coli and P. aeruginosa), Gram-positive (S. aureus and E. faecalis), and fungi (C. albicans) employing both agar disk diffusion and minimum inhibitory concentration (MICs) methods. Copper oxide nanoparticles showed more sensitivity towards four bacterial microorganisms than the other two chalcogenides followed by copper sulfide nanoparticles with copper selenide nanoparticles being the least sensitive. The sensitivity of copper oxide nanoparticles is attributed to the smaller size of oxygen atom which strongly affects its reactivity and stability and hence very stable and highly reactive compared to sulfur and selenium.
{"title":"Antimicrobial Activity of the Synthesized of Copper Chalcogenide Nanoparticles","authors":"N. G. Mbewana-Ntshanka, M. Moloto, P. K. Mubiayi","doi":"10.1155/2021/6675145","DOIUrl":"https://doi.org/10.1155/2021/6675145","url":null,"abstract":"Antimicrobial activity of copper chalcogenides nanoparticles was investigated by synthesizing copper selenide, copper sulfide, and copper oxide via the hot-injection method. Since reaction time has a profound effect on the nanocrystals size and shapes, the effect of reaction time was also investigated during the synthesis of the copper chalcogenides to obtain nanocrystals with desired properties. The reaction time showed no effect on the phase composition of the synthesized copper sulfide, copper oxide, and copper selenide nanoparticles. However, the size variation of nanoparticles with different reaction time was observed. Reaction time of 30 minutes gave the best optical (the shape of the absorption band edge and emission maxima values) and structural (size distribution of particles) properties for CuSe and CuS compared to other reaction times (15, 45, and 60 min). Their band edges were located at 506 (2.45 eV) and 538 nm (2.30 eV), respectively. For this reaction time, copper selenide produced nanoparticles with a size range of 1–27 nm and copper sulfide nanoparticles ranged 1–18 nm. The morphologies of both chalcogenides at 30 min reaction time were spherical. Reaction time of 15 minutes gave the best optical and structural properties for copper oxide nanoparticles with a band edge of 454 nm (2.73 eV) and particle size ranging 0.8–3.2 nm, but nonetheless, 30 min was used as the optimum reaction time for all three chalcogenides. The optimum parameter (220°C, 30 min, and 1 : 1 ratio) was used to synthesize the three copper chalcogenides which were then tested against Gram-negative (E. coli and P. aeruginosa), Gram-positive (S. aureus and E. faecalis), and fungi (C. albicans) employing both agar disk diffusion and minimum inhibitory concentration (MICs) methods. Copper oxide nanoparticles showed more sensitivity towards four bacterial microorganisms than the other two chalcogenides followed by copper sulfide nanoparticles with copper selenide nanoparticles being the least sensitive. The sensitivity of copper oxide nanoparticles is attributed to the smaller size of oxygen atom which strongly affects its reactivity and stability and hence very stable and highly reactive compared to sulfur and selenium.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"60 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2021-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77183910","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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