scholarly journals Selective Mineralization and Recovery of Au(III) from Multi-Ionic Aqueous Systems by Bacillus licheniformis FZUL-63

Minerals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 392
Author(s):  
Yangjian Cheng ◽  
Zhibin Ke ◽  
Xiaojing Bian ◽  
Jianhua Zhang ◽  
Zhen Huang ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Bacillus Licheniformis ◽  
Photoelectron Spectroscopy ◽  
Precious Metals ◽  
Aqueous Systems ◽  
Tem Analysis ◽  
X Ray ◽  
Practical Applications ◽  
Bacterial Surface ◽  
20 Nm

The recovery of precious metals is a project with both economic and environmental significance. In this paper, how to use bacterial mineralization to selectively recover gold from multi-ionic aqueous systems is presented. The Bacillus licheniformis FZUL-63, isolated from a landscape lake in Fuzhou University, was shown to selectively mineralize and precipitate gold from coexisting ions in aqueous solution. The removal of Au(III) almost happened in the first hour. Scanning electron microscope with X-ray energy dispersive spectroscopy (SEM/EDS-mapping) results and fourier transform infrared spectroscopy (FTIR) data show that the amino, carboxyl, and phosphate groups on the surface of the bacteria are related to the adsorption of gold ions. X-ray photoelectron spectroscopy (XPS) results implied that Au(III) ions were reduced to those that were monovalent, and the Au(I) was then adsorbed on the bacterial surface at the beginning stage (in the first hour). X-ray diffraction (XRD) results showed that the gold biomineralization began about 10 h after the interaction between Au(III) ions and bacteria. Au(III) mineralization has rarely been influenced by other co-existing metal ions. Transmission electron microscope (TEM) analysis shows that the gold nanoparticles have a polyhedral structure with a particle size of ~20 nm. The Bacillus licheniformis FZUL-63 could selectively mineralize and recover 478 mg/g (dry biomass) gold from aqua regia-based metal wastewater through four cycles. This could be of great potential in practical applications.

scholarly journals Selective Mineralization and Recovery of Au(III) from Multi-ionic Aqueous Systems by Microorganisms

2019 ◽  
Author(s):  
Yangjian Cheng ◽  
Zhibin Ke ◽  
Xiaojing Bian ◽  
Jianhua Zhang ◽  
Zhen Huang ◽  
...  
Keyword(s):  
Bacillus Licheniformis ◽  
Precious Metals ◽  
Aqueous Systems ◽  
Tem Analysis ◽  
Aqua Regia ◽  
Bacterial Surface ◽  
Landscape Lake ◽  
20 Nm ◽  
Coexisting Ions ◽  
Phosphate Groups

The recovery of precious metals is a project with both economic and environmental significance. In this paper, it presents how to use bacterial mineralization to selectively recover gold from multi-ionic aqueous systems. The Bacillus licheniformis FZUL-63, separated from a landscape lake in FuZhou University, was shown to selectively mineralize and precipitate gold from coexisting ions in aqueous solution. The removal of Au(III) was almost happened in first hour, and FTIR data show that the amino, carboxyl and phosphate groups on the surface of the bacteria are related to the adsorption of gold ions. XPS results implied that Au(III) ions are reduced to monovalent, and then the Au(I) was adsorbed on the bacterial surface at the beginning stage(first hour). XRD results showed the gold biomineralization began about 10 hours after the interaction between Au(III) ions and bacteria. The Au(III) mineralization has been rarely influenced by other co-existing metal ions. TEM analysis shows the gold nanoparticles are polyhedral structure with a particle size of ~20 nm. The Bacillus licheniformis FZUL-63 could selectively mineralize and recover 478 mg/g(dry biomass) gold from aqua regia-based metal wastewater through four cycles. It could be of great potential in the practical application.

Large-scale synthesis of amorphous phosphorus nitride imide nanotubes with high luminescent properties

2005 ◽  
Vol 20 (2) ◽  
pp. 325-330 ◽  
Author(s):  
Qixun Guo ◽  
Qing Yang ◽  
Lei Zhu ◽  
Chengqi Yi ◽  
Yi Xie
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Large Scale ◽  
Luminescent Properties ◽  
Atomic Ratio ◽  
Binding Energies ◽  
X Ray ◽  
Microscope Images ◽  
Large Scale Synthesis ◽  
20 Nm

A facile solvothermal approach was successfully developed for the large-scale synthesis of amorphous phosphorus nitride imide (H3xP3N5+x) nanotubes with high luminescent properties by the reaction of 1,3,5-hexachlorotriphosphazene (P3N3Cl6) with sodium amide (NaNH2) at low temperatures. Transmission electron microscope images showed that the inner diameter of nanotubes is 120 ± 20 nm, wall thickness is 40 ± 10 nm, and length ranges from several to ten micrometers. Scanning electron microscope images revealed that the proportion of the nanotubes exceeds 90%. X-ray photoelectron spectroscopy spectra indicated that the binding energies of P2p and N1s are 133.30 and 398.40 eV, respectively, and the atomic ratio of P:N is 3:5.13. The infrared spectra of the sample are comparable to those of the reported HPN2 and HP4N7. Thermogravimetric analysis revealed that the product is very robust in a nonoxidizing atmosphere. The structure and the optical properties of the product and the annealed samples were investigated by x-ray diffraction and photoluminescence measurements, respectively.

scholarly journals Muntingia calabura Leaves Mediated Green Synthesis of CuO Nanorods: Exploiting Phytochemicals for Unique Morphology

Materials ◽  
2021 ◽  
Vol 14 (21) ◽  
pp. 6379
Author(s):  
Vidhya Selvanathan ◽  
Mohammod Aminuzzaman ◽  
Lai-Hock Tey ◽  
Syaza Amira Razali ◽  
Khaled Althubeiti ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Nanoparticle Synthesis ◽  
Xrd Analysis ◽  
Leaf Extracts ◽  
Tem Analysis ◽  
X Ray ◽  
Cuo Nps ◽  
Muntingia Calabura ◽  
Cuo Nanorods

In this study, phytochemical assisted nanoparticle synthesis was performed using Muntingia calabura leaf extracts to produce copper oxide nanoparticles (CuO NPs) with interesting morphology. Scanning electron microscope (SEM) and transmission electron microscope (TEM) analysis of the biosynthesized CuO NPs reveal formation of distinct, homogeneous, and uniform sized CuO nanorods structure with thickness and length of around 23 nm and 79 nm, respectively. Based on Fourier-transform infrared (FTIR) analysis, the unique combinations of secondary metabolites such as flavonoid and polyphenols in the plant extract are deduced to be effective capping agents to produce nanoparticles with unique morphologies similar to conventional chemical synthesis. X-ray diffraction (XRD) analysis verified the monoclinical, crystalline structure of the CuO NPs. The phase purity and chemical identity of the product was consolidated via X-Ray photoelectron spectroscopy (XPS) and Raman spectroscopic data which indicate the formation of a single phase CuO without the presence of other impurities. The direct and indirect optical band gap energies of the CuO nanorods were recorded to be 3.65 eV and 1.42 eV.

scholarly journals Synthesis and Characterization of Pyrochlore Bi2Sn2O7Doping with Praseodymium by Hydrothermal Method and Its Photocatalytic Activity Study

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Weicheng Xu ◽  
Guangyin Zhou ◽  
Jianzhang Fang ◽  
Zhang Liu ◽  
YunFang Chen ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Visible Light ◽  
Hydrothermal Method ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray ◽  
Transmission Electron ◽  
20 Nm ◽  
Adsorption Desorption

Praseodymium doped Bi2Sn2O7(BSO), as a visible-light responsive photocatalyst, was prepared by a hydrothermal method with different dopant contents. The as-prepared photocatalysts were investigated by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), N2adsorption-desorption isotherm, X-ray photoelectron spectroscopy analysis (XPS), and UV-Vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity of prepared catalysts was evaluated by the degradation of Rhodamine Bextra (RhB) and 2,4-dichlorophenol (2,4-DCP) in aqueous solution under visible light irradiation. It was found that Pr doping inhibited the growth of crystalline size and the as-prepared materials were small in size (10–20 nm). In our experiments, Pr-doped BSO samples exhibited enhanced visible-light photocatalytic activity compared to the undoped BSO, and the optimal dopant amount of Pr was 1.0 mol% for the best photocatalytic activity. On the basis of the calculated PL spectra, the mechanism of enhanced photocatalytic activity has been discussed.

The effect of Tin additionon on Structural and magnetic properties of the stannoferrite Li0.5+0.5XFe2.5-1.5XSnXO4

2016 ◽  
Vol 12 (3) ◽  
pp. 4307-4321 ◽  
Author(s):  
Ahmed Hassan Ibrahim ◽  
Yehia Abbas
Keyword(s):  
Particle Size ◽  
Fine Particles ◽  
Magnetic Moments ◽  
Lithium Ferrite ◽  
Tem Analysis ◽  
Weiss Temperature ◽  
X Ray ◽  
Two Phases ◽  
Nanocrystalline Ferrite ◽  
20 Nm

The physical properties of ferrites are verysensitive to microstructure, which in turn critically dependson the manufacturing process.Nanocrystalline Lithium Stannoferrite system Li0.5+0.5XFe2.5-1.5XSnXO4,X= (0, 0.2, 0.4, 0.6, 0.8 and 1.0) fine particles were successfully prepared by double sintering ceramic technique at pre-sintering temperature of 500oC for 3 h andthepre-sintered material was crushed and sintered finally in air at 1000oC.The structural and microstructural evolutions of the nanophase have been studied using X-ray powder diffraction (XRD) and the Rietveld method.The refinement results showed that the nanocrystalline ferrite has a two phases of ordered and disordered phases for polymorphous lithium Stannoferrite.The particle size of as obtained samples were found to be ~20 nm through TEM that increases up to ~ 85 nmand isdependent on the annealing temperature. TEM micrograph reveals that the grains of sample are spherical in shape. (TEM) analysis confirmed the X-ray results.The particle size of stannic substituted lithium ferrite fine particle obtained from the XRD using Scherrer equation.Magneticmeasurements obtained from lake shore’s vibrating sample magnetometer (VSM), saturation magnetization ofordered LiFe5O8 was found to be (57.829 emu/g) which was lower than disordered LiFe5O8(62.848 emu/g).Theinterplay between superexchange interactions of Fe3+ ions at A and B sublattices gives rise to ferrimagnetic ordering of magnetic moments,with a high Curie-Weiss temperature (TCW ~ 900 K).

scholarly journals Preparation and Characterization of Visible-Light-Activated Fe-N Co-Doped TiO2and Its Photocatalytic Inactivation Effect on Leukemia Tumors

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Kangqiang Huang ◽  
Li Chen ◽  
Jianwen Xiong ◽  
Meixiang Liao
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Light Therapy ◽  
Cell Counting ◽  
Visible Absorption ◽  
X Ray ◽  
Photocatalytic Inactivation ◽  
Inactivation Efficiency ◽  
Co Doped

The Fe-N co-doped TiO2nanocomposites were synthesized by a sol-gel method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectroscopy (UV-vis) and X-ray photoelectron spectroscopy (XPS). Then the photocatalytic inactivation of Fe-N-doped TiO2on leukemia tumors was investigated by using Cell Counting Kit-8 (CCK-8) assay. Additionally, the ultrastructural morphology and apoptotic percentage of treated cells were also studied. The experimental results showed that the growth of leukemic HL60 cells was significantly inhibited in groups treated with TiO2nanoparticles and the photocatalytic activity of Fe-N-TiO2was significantly higher than that of Fe-TiO2and N-TiO2, indicating that the photocatalytic efficiency could be effectively enhanced by the modification of Fe-N. Furthermore, when 2 wt% Fe-N-TiO2nanocomposites at a final concentration of 200 μg/mL were used, the inactivation efficiency of 78.5% was achieved after 30-minute light therapy.

Preparation of Carbon Nanofibers from Polyacrylonitrile Nanofibers by Electrospinning

2011 ◽  
Vol 415-417 ◽  
pp. 642-647
Author(s):  
En Zhong Li ◽  
Da Xiang Yang ◽  
Wei Ling Guo ◽  
Hai Dou Wang ◽  
Bin Shi Xu
Keyword(s):  
Electron Microscope ◽  
Carbon Nanofibers ◽  
Photoelectron Spectroscopy ◽  
Solution Concentration ◽  
Dimethyl Formamide ◽  
Ultrafine Fibers ◽  
X Ray ◽  
Scanning Electron ◽  
Pan Fibers

Ultrafine fibers were electrospun from polyacrylonitrile (PAN)/N,N-dimethyl formamide (DMF) solution as a precursor of carbon nanofibers. The effects of solution concentration, applied voltage and flow rate on preparation and morphologies of electrospun PAN fibers were investigated. Morphologies of the green fibers, stabilized fibers and carbonized fibers were compared by scanning electron microscope (SEM). The diameter of PAN nanofibers is about 450nm and the distribution of diameter is well-proportioned. Characterization of the elements changes of fibers were performed by X-ray photoelectron spectroscopy (XPS).

Low-temperature route to nanoscale P3N5 hollow spheres

2003 ◽  
Vol 18 (10) ◽  
pp. 2359-2363 ◽  
Author(s):  
Hongzhou Gu ◽  
Yunle Gu ◽  
Zhefeng Li ◽  
Yongcheng Ying ◽  
Yitai Qian
Keyword(s):  
Photoelectron Spectroscopy ◽  
Hollow Spheres ◽  
Molar Ratio ◽  
Visible Absorption ◽  
X Ray ◽  
Transmission Electron ◽  
Influence Of Temperature On ◽  
Wide Gap ◽  
20 Nm ◽  
High Degree

Nanoscale hollow spheres of amorphous phosphorus nitride (P3N5) were synthesized by reacting PCl3 with NaN3 at 150–250 °C. Transmission electron microscope images show that the hollow spheres have a diameter of 150–350 nm, and the thickness of the shell is 20 nm. A very small amount of curly films were also found in the sample prepared at 150 °C. The infrared spectrum indicates a high degree of purity. X-ray photoelectron spectroscopy indicates the presence of P and N, with a molar ratio of 1:1.62 for P:N. Ultraviolet-visible absorption spectroscopy shows an absorption band at 265–315 nm. Under photoluminescent excitation at 230 nm, the P3N5 emits ultraviolet light at 305 nm. With a band gap of 4.28 eV, the products may be a wide gap semiconductor. A possible mechanism and the influence of temperature on the formation of the hollow spheres are also discussed.

scholarly journals Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV-Irradiation

2018 ◽  
Author(s):  
Irwing M. Ramírez-Sánchez ◽  
Erick R. Bandala
Keyword(s):  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Transmission Electron ◽  
Iron Doped

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

scholarly journals Fenton Degradation of Ofloxacin Using a Montmorillonite-Fe3O4 Composite

2020 ◽  
Vol 2 (1) ◽  
pp. 32
Author(s):  
Alamri Rahmah Dhahawi Ahmad ◽  
Saifullahi Shehu Imam ◽  
Wen Da Oh ◽  
Rohana Adnan
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
High Efficiency ◽  
Solar Irradiation ◽  
Precipitation Process ◽  
Wastewater Remediation ◽  
Solution Ph ◽  
X Ray ◽  
Subsequent Degradation ◽  
Co Precipitation

In this work, FeM composites consisting of montmorillonite and variable amounts of Fe3O4 were successfully synthesized via a facile co-precipitation process. They were characterized using X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscope (TEM), N2 adsorption-desorption, and Fourier transform infrared spectroscopy (FT-IR) techniques to explain the effect of Fe3O4 content on the physicochemical properties of the Fe3O4-montmorillonite (FeM) composites. The FeM composites were subsequently used as heterogeneous Fenton catalysts to activate green oxidant (H2O2) for the subsequent degradation of ofloxacin (OFL) antibiotic. The efficiency of the FeM composites was studied by varying various parameters of Fe3O4 loading on montmorillonite, catalyst dosage, initial solution pH, initial OFL concentration, different oxidants, H2O2 dosage, reaction temperature, inorganic salts, and solar irradiation. Under the conditions of 0.75 g/L FeM-10, 5 mL/L H2O2, and natural pH, almost 81% of 50 mg/L of OFL was removed within 120 min in the dark, while total organic carbon (TOC) reduction was about 56%. Moreover, the FeM-10 composite maintained high efficiency and was stable even after four continuous cycles, making it a promising candidate in real wastewater remediation.

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