The crystallographic features of pearlite were investigated by experiments and edge-to-edge matching principle. Two new orientation relationships between ferrite and cementite were determinated by selected area electr...The crystallographic features of pearlite were investigated by experiments and edge-to-edge matching principle. Two new orientation relationships between ferrite and cementite were determinated by selected area electron diffraction and then explained by our modified edge-to-edge matching method. The consistence of the experimental results with theoretical prediction confirms the practicability of the modified edge-to-edge matching model.展开更多
The microstructures of copper liners of shaped charges prepared byelectroforming technique were investigated by transmission electron microscopy (TEM). Meanwhile, theorientations distributing of the grains in the elec...The microstructures of copper liners of shaped charges prepared byelectroforming technique were investigated by transmission electron microscopy (TEM). Meanwhile, theorientations distributing of the grains in the electroformed copper liners of shaped charges wasexamined by the electron backscattering Kikuchi pattern (EBSP) technique. TEM observations haverevealed that these electroformed copper liners of shaped charges have the grain size of about 1-3mu m and the grains have a preferential orientation distribution along the growth direction. EBSPanalysis has demonstrated that the as-formed copper liners of shaped charges exhibit amicro-texture, i.e. one type of fiber texture, and the preferred growth direction is normal to thesurface of the liners.展开更多
Microstructures of a CuZnAlMnNi shape memory alloy in the as-quenched andlong-term aged conditions were investigated by transmission electron microscopy. Aged for one yearin martensite phase, an equilibrium α-phase w...Microstructures of a CuZnAlMnNi shape memory alloy in the as-quenched andlong-term aged conditions were investigated by transmission electron microscopy. Aged for one yearin martensite phase, an equilibrium α-phase with fcc structure was observed in the M18R martensitematrix, accompanied by the appearance of a novel diffraction pattern. By analysis, it was suggestedthat the novel pattern results from the α-phase and the martensite matrix remaining in seven fineplates which produce intense secondary diffraction effect when the diffraction beams enter from onephase into another.展开更多
Solid phase reactions of Cr（Ⅵ） with Fe（0） were investigated with spherical-aberration-corrected scanning transmission electron microscopy（Cs-STEM） integrated with X-ray energy-dispersive spectroscopy（XEDS）. N...Solid phase reactions of Cr（Ⅵ） with Fe（0） were investigated with spherical-aberration-corrected scanning transmission electron microscopy（Cs-STEM） integrated with X-ray energy-dispersive spectroscopy（XEDS）. Near-atomic resolution elemental mappings of Cr（Ⅵ）–Fe（0） reactions were acquired. Experimental results show that rate and extent of Cr（Ⅵ） encapsulation are strongly dependent on the initial concentration of Cr（Ⅵ） in solution. Low Cr loading in nZⅥ（〈1.0 wt%） promotes the electrochemical oxidation and continuous corrosion of n ZⅥ while high Cr loading（〉1.0 wt%） can quickly shut down the Cr uptake. With the progress of iron oxidation and dissolution, elements of Cr and O counter-diffuse into the nanoparticles and accumulate in the core region at low levels of Cr（Ⅵ）（e.g., 〈 10 mg/L）. Whereas the reacted n ZⅥ is quickly coated with a newly-formed layer of 2–4 nm in the presence of concentrated Cr（Ⅵ）（e.g., 〉 100 mg/L）. The passivation structure is stable over a wide range of pH unless pH is low enough to dissolve the passivation layer. X-ray photoelectron spectroscopy（XPS） depth profiling reconfirms that the composition of the newly-formed surface layer consists of Fe（Ⅲ）–Cr（Ⅲ）（oxy）hydroxides with Cr（Ⅵ） adsorbed on the outside surface. The insoluble and insulating Fe（Ⅲ）–Cr（Ⅲ）（oxy）hydroxide layer can completely cover the n ZⅥ surface above the critical Cr loading and shield the electron transfer. Thus, the fast passivation of nZⅥ in high Cr（Ⅵ） solution is detrimental to the performance of nZⅥ for Cr（Ⅵ） treatment and remediation.展开更多
In this study, an ecofriendly and economically viable waste management approach have been attempted towards the biosynthesis of agriculturally important nanoparticles from jarosite waste. Aspergillus terreus strain J4...In this study, an ecofriendly and economically viable waste management approach have been attempted towards the biosynthesis of agriculturally important nanoparticles from jarosite waste. Aspergillus terreus strain J4 isolated from jarosite（waste from Debari Zinc Smelter,Udaipur, India）, showed good leaching efficiency along with nanoparticles（NPs） formation under ambient conditions. Fourier-transform infrared spectroscopy（FT-IR） and transmission electron microscopy（TEM） confirmed the formation of NPs. Energy dispersive X-ray spectroscopy（EDX analysis） showed strong signals for zinc, iron, calcium and magnesium,with these materials being leached out. TEM analysis and high resolution transmission electron microscopy（HRTEM） showed semi-quasi spherical particles having average size of 10‐50 nm. Thus, a novel biomethodology was developed using fungal cell-free extract for bioleaching and subsequently nanoconversion of the waste materials into nanostructured form. These biosynthesized nanoparticles were tested for their efficacy on seed emergence activity of wheat（Triticum aestivum） seeds and showed enhanced growth at concentration of 20 ppm. These nanomaterials are expected to enhance plant growth properties and being targeted as additives in soil fertility and crop productivity enhancement.展开更多
Lipids exhibit an extraordinary polymorphism in self-assembled mesophases, with lamellar phases as the most relevant biological representative. To mimic lipid lamellar phases with amphiphilic designer peptides, seven ...Lipids exhibit an extraordinary polymorphism in self-assembled mesophases, with lamellar phases as the most relevant biological representative. To mimic lipid lamellar phases with amphiphilic designer peptides, seven systematically varied short peptides were engineered. Indeed, four peptide candidates （V4D, V4WD, V4WD2, I4WD2） readily self-assembled into lamellae in aqueous solution. Small-angle X-ray scattering （SAXS） patterns revealed ordered lamellar structures with a repeat distance of 4-5 nm. Transmission electron microscopy （TEM） images confirmed the presence of stacked sheets. Two derivatives （V3D and V4D2） remained as loose aggregates dispersed in solution; one peptide （L4WD2） formed twisted tapes with internal lameUae and an antiparaUel -type monomer aligrtment. To understand the interaction of peptides with lipids, they were mixed with phosphatidylcholines. Low peptide concentrations （1.1 mM） induced the formation of a heterogeneous mixture of vesicular structures. Large multilamellar vesicles （MLV, d-spacing - 6.3 nm） coexisted with oligo- or unilamellar vesicles （- 50 nm in diameter） and bicelle-like structures （- 45 nm length, - 18 nm width）. High peptide concentrations （11 mM） led to unilamellar vesicles （ULV, diameter - 260-280 nm） with a homogeneous mixing of lipids and peptides. SAXS revealed the temperature-dependent fine structure of these ULVs. At 25 ℃ the bilayer is in a fully Interdigitated state （headgroup-to-headgroup distance dH, -2.9 nm）, whereas at 50 ℃this interdigitation opens up （dtm- 3.6 nm）. Our results highlight the versatility of self-assembled peptide superstructures. Subtle changes in the amino acid composition are key design elements in creating peptide- or lipid- peptide nanostructures with richness in morphology similar to that of naturally occurrin~ lioids.展开更多
The results presented in this study were concerned with microstructures and mechanical properties of poly- crystalline Cu subjected to plastic deformation by a compression with oscillatory torsion process. Different d...The results presented in this study were concerned with microstructures and mechanical properties of poly- crystalline Cu subjected to plastic deformation by a compression with oscillatory torsion process. Different deformation parameters of the compression with oscillatory torsion process were adopted to study their effects on the microstructure and mechanical properties. The deformed microstructure was characterized quantitatively by electron backscattered diffraction （EBSD） and scanning transmission electron microscopy （STEM）. Mechanical properties were determined on an MTS QTest/10 machine equipped with digital image correlation. From the experimental results, processes performed at high compression speed and high torsion frequency are recommended for refining the grain size. The size of structure elements, such as average grain size （D） and subgrain size （d）, reached 0.42 μm and 0.30 μm, respectively, and the fraction of high angle boundaries was 35% when the sample was deformed at a torsion frequency f = 1.6 Hz and compression rate v= 0.04 mm/s. These deformation parameters led to an improvement in the strength properties. The material exhibited an ultimate tensile strength （UTS） of 434 MPa and a yield strength （YS） of 418 MPa. These values were about two times greater than those of the initial state.展开更多
Nanocrystalline CdS thin films have been deposited using precursors with different thiourea concentrationonto glass substrates by sol-gel spin coating method.The crystalline nature of the films has been observedto be ...Nanocrystalline CdS thin films have been deposited using precursors with different thiourea concentrationonto glass substrates by sol-gel spin coating method.The crystalline nature of the films has been observedto be strongly dependent on thiourea concentration and annealing temperature.The CdS films are found tobe nanocrystalline in nature with hexagonal structure.The grain size is found to be in the range of 7.6 to11.5 nm depending on the thiourea concentration and annealing temperature.The high resolution transmissionelectron microscopy （HRTEM） results of the CdS films prepared using cadmium to thiourea molar ratio of0.3：0.3 indicate the formation of nanocrystalline CdS with grain size of 5 nm.Fourier transform infrared （FTIR）analysis shows the absorption bands corresponding to Cd and S.The optical study carried out to determinethe band gap of the nanostructured CdS thin films shows a strong blue shift.The band gap energy has beenobserved to lie in the range of 3.97 to 3.62 eV following closely the quantum confinement dependence ofenergy on crystallite radius.The dependence of band gap of the CdS films on the annealing temperature andthiourea concentration has also been studied.The photoluminescence （PL） spectra display two main emissionpeaks corresponding to the blue and green emissions of CdS.展开更多
In this study, self assembly behavior was induced for γ-alumina nanoparticles by adsorption of dimethyl disulfide. Following this trend, we have developed a chemical process to obtain ＇y-alumina in the nano scale. S...In this study, self assembly behavior was induced for γ-alumina nanoparticles by adsorption of dimethyl disulfide. Following this trend, we have developed a chemical process to obtain ＇y-alumina in the nano scale. Scanning electron microscopy images of the prepared γ-alumina showed big and strong agglomeration of the nanoparticles indicating that these nanoparticles have strong surface forces. Transmission electron microscopy images confirmed that the γ-alumina nanoparticles 3-7 nm in size were converted to uniform spherical shape in the size range of 1-2 mm after shaking with dimethyl disulfide in the presence of n-hexane at room temperature. This phenomenon did not appear in the case of alumina in the micro scale. The surface properties of the prepared γ-alumina in the nano scale were characterized and compared with the γ-alumina in the micro scale by using low temperature nitrogen adsorption-desorption system, indicating that the specific surface area of the prepared γ-alumina nanoparticles is larger than that of the γ-alumina in the micro scale. Furthermore, micro- and meso-pores were observed for the if-alumina nanoparticles while only mesoporous structure was detected for the γ-alumina in the micro scale. These experimental results suggested that the self assembly behavior of the γ-alumina nanoparticles may be due to the selective adsorption ofdimethyl disulfide in the micropores of these nanoparticles to act as bridge linking the nanoparticles.展开更多
基金supported by the National Natural Science Foundation of China (Grant Nos.51001069 and 51031001)
文摘The crystallographic features of pearlite were investigated by experiments and edge-to-edge matching principle. Two new orientation relationships between ferrite and cementite were determinated by selected area electron diffraction and then explained by our modified edge-to-edge matching method. The consistence of the experimental results with theoretical prediction confirms the practicability of the modified edge-to-edge matching model.
基金the National Natural Science Foundation of China (No. 59971008)
文摘The microstructures of copper liners of shaped charges prepared byelectroforming technique were investigated by transmission electron microscopy (TEM). Meanwhile, theorientations distributing of the grains in the electroformed copper liners of shaped charges wasexamined by the electron backscattering Kikuchi pattern (EBSP) technique. TEM observations haverevealed that these electroformed copper liners of shaped charges have the grain size of about 1-3mu m and the grains have a preferential orientation distribution along the growth direction. EBSPanalysis has demonstrated that the as-formed copper liners of shaped charges exhibit amicro-texture, i.e. one type of fiber texture, and the preferred growth direction is normal to thesurface of the liners.
基金This project is financially supported by the Natural Science Foundation of Shandong Province ( Y2001F06) and the Fund for Outstanding Young Researcher of Shandong Province
文摘Microstructures of a CuZnAlMnNi shape memory alloy in the as-quenched andlong-term aged conditions were investigated by transmission electron microscopy. Aged for one yearin martensite phase, an equilibrium α-phase with fcc structure was observed in the M18R martensitematrix, accompanied by the appearance of a novel diffraction pattern. By analysis, it was suggestedthat the novel pattern results from the α-phase and the martensite matrix remaining in seven fineplates which produce intense secondary diffraction effect when the diffraction beams enter from onephase into another.
基金supported by the National Natural Science Foundation of China(Nos.21677107,51578398)the Fundamental Research Funds for the Central Universities(No.0400219363)
文摘Solid phase reactions of Cr（Ⅵ） with Fe（0） were investigated with spherical-aberration-corrected scanning transmission electron microscopy（Cs-STEM） integrated with X-ray energy-dispersive spectroscopy（XEDS）. Near-atomic resolution elemental mappings of Cr（Ⅵ）–Fe（0） reactions were acquired. Experimental results show that rate and extent of Cr（Ⅵ） encapsulation are strongly dependent on the initial concentration of Cr（Ⅵ） in solution. Low Cr loading in nZⅥ（〈1.0 wt%） promotes the electrochemical oxidation and continuous corrosion of n ZⅥ while high Cr loading（〉1.0 wt%） can quickly shut down the Cr uptake. With the progress of iron oxidation and dissolution, elements of Cr and O counter-diffuse into the nanoparticles and accumulate in the core region at low levels of Cr（Ⅵ）（e.g., 〈 10 mg/L）. Whereas the reacted n ZⅥ is quickly coated with a newly-formed layer of 2–4 nm in the presence of concentrated Cr（Ⅵ）（e.g., 〉 100 mg/L）. The passivation structure is stable over a wide range of pH unless pH is low enough to dissolve the passivation layer. X-ray photoelectron spectroscopy（XPS） depth profiling reconfirms that the composition of the newly-formed surface layer consists of Fe（Ⅲ）–Cr（Ⅲ）（oxy）hydroxides with Cr（Ⅵ） adsorbed on the outside surface. The insoluble and insulating Fe（Ⅲ）–Cr（Ⅲ）（oxy）hydroxide layer can completely cover the n ZⅥ surface above the critical Cr loading and shield the electron transfer. Thus, the fast passivation of nZⅥ in high Cr（Ⅵ） solution is detrimental to the performance of nZⅥ for Cr（Ⅵ） treatment and remediation.
文摘In this study, an ecofriendly and economically viable waste management approach have been attempted towards the biosynthesis of agriculturally important nanoparticles from jarosite waste. Aspergillus terreus strain J4 isolated from jarosite（waste from Debari Zinc Smelter,Udaipur, India）, showed good leaching efficiency along with nanoparticles（NPs） formation under ambient conditions. Fourier-transform infrared spectroscopy（FT-IR） and transmission electron microscopy（TEM） confirmed the formation of NPs. Energy dispersive X-ray spectroscopy（EDX analysis） showed strong signals for zinc, iron, calcium and magnesium,with these materials being leached out. TEM analysis and high resolution transmission electron microscopy（HRTEM） showed semi-quasi spherical particles having average size of 10‐50 nm. Thus, a novel biomethodology was developed using fungal cell-free extract for bioleaching and subsequently nanoconversion of the waste materials into nanostructured form. These biosynthesized nanoparticles were tested for their efficacy on seed emergence activity of wheat（Triticum aestivum） seeds and showed enhanced growth at concentration of 20 ppm. These nanomaterials are expected to enhance plant growth properties and being targeted as additives in soil fertility and crop productivity enhancement.
文摘Lipids exhibit an extraordinary polymorphism in self-assembled mesophases, with lamellar phases as the most relevant biological representative. To mimic lipid lamellar phases with amphiphilic designer peptides, seven systematically varied short peptides were engineered. Indeed, four peptide candidates （V4D, V4WD, V4WD2, I4WD2） readily self-assembled into lamellae in aqueous solution. Small-angle X-ray scattering （SAXS） patterns revealed ordered lamellar structures with a repeat distance of 4-5 nm. Transmission electron microscopy （TEM） images confirmed the presence of stacked sheets. Two derivatives （V3D and V4D2） remained as loose aggregates dispersed in solution; one peptide （L4WD2） formed twisted tapes with internal lameUae and an antiparaUel -type monomer aligrtment. To understand the interaction of peptides with lipids, they were mixed with phosphatidylcholines. Low peptide concentrations （1.1 mM） induced the formation of a heterogeneous mixture of vesicular structures. Large multilamellar vesicles （MLV, d-spacing - 6.3 nm） coexisted with oligo- or unilamellar vesicles （- 50 nm in diameter） and bicelle-like structures （- 45 nm length, - 18 nm width）. High peptide concentrations （11 mM） led to unilamellar vesicles （ULV, diameter - 260-280 nm） with a homogeneous mixing of lipids and peptides. SAXS revealed the temperature-dependent fine structure of these ULVs. At 25 ℃ the bilayer is in a fully Interdigitated state （headgroup-to-headgroup distance dH, -2.9 nm）, whereas at 50 ℃this interdigitation opens up （dtm- 3.6 nm）. Our results highlight the versatility of self-assembled peptide superstructures. Subtle changes in the amino acid composition are key design elements in creating peptide- or lipid- peptide nanostructures with richness in morphology similar to that of naturally occurrin~ lioids.
基金supported by the Polish Ministry of Science and Higher Education under research project No. N N507 373435
文摘The results presented in this study were concerned with microstructures and mechanical properties of poly- crystalline Cu subjected to plastic deformation by a compression with oscillatory torsion process. Different deformation parameters of the compression with oscillatory torsion process were adopted to study their effects on the microstructure and mechanical properties. The deformed microstructure was characterized quantitatively by electron backscattered diffraction （EBSD） and scanning transmission electron microscopy （STEM）. Mechanical properties were determined on an MTS QTest/10 machine equipped with digital image correlation. From the experimental results, processes performed at high compression speed and high torsion frequency are recommended for refining the grain size. The size of structure elements, such as average grain size （D） and subgrain size （d）, reached 0.42 μm and 0.30 μm, respectively, and the fraction of high angle boundaries was 35% when the sample was deformed at a torsion frequency f = 1.6 Hz and compression rate v= 0.04 mm/s. These deformation parameters led to an improvement in the strength properties. The material exhibited an ultimate tensile strength （UTS） of 434 MPa and a yield strength （YS） of 418 MPa. These values were about two times greater than those of the initial state.
文摘Nanocrystalline CdS thin films have been deposited using precursors with different thiourea concentrationonto glass substrates by sol-gel spin coating method.The crystalline nature of the films has been observedto be strongly dependent on thiourea concentration and annealing temperature.The CdS films are found tobe nanocrystalline in nature with hexagonal structure.The grain size is found to be in the range of 7.6 to11.5 nm depending on the thiourea concentration and annealing temperature.The high resolution transmissionelectron microscopy （HRTEM） results of the CdS films prepared using cadmium to thiourea molar ratio of0.3：0.3 indicate the formation of nanocrystalline CdS with grain size of 5 nm.Fourier transform infrared （FTIR）analysis shows the absorption bands corresponding to Cd and S.The optical study carried out to determinethe band gap of the nanostructured CdS thin films shows a strong blue shift.The band gap energy has beenobserved to lie in the range of 3.97 to 3.62 eV following closely the quantum confinement dependence ofenergy on crystallite radius.The dependence of band gap of the CdS films on the annealing temperature andthiourea concentration has also been studied.The photoluminescence （PL） spectra display two main emissionpeaks corresponding to the blue and green emissions of CdS.
基金supported through Annual Research Grants Program (ARP-29-111) by King Abdulaziz City for Scienceand Technology (KACST)
文摘In this study, self assembly behavior was induced for γ-alumina nanoparticles by adsorption of dimethyl disulfide. Following this trend, we have developed a chemical process to obtain ＇y-alumina in the nano scale. Scanning electron microscopy images of the prepared γ-alumina showed big and strong agglomeration of the nanoparticles indicating that these nanoparticles have strong surface forces. Transmission electron microscopy images confirmed that the γ-alumina nanoparticles 3-7 nm in size were converted to uniform spherical shape in the size range of 1-2 mm after shaking with dimethyl disulfide in the presence of n-hexane at room temperature. This phenomenon did not appear in the case of alumina in the micro scale. The surface properties of the prepared γ-alumina in the nano scale were characterized and compared with the γ-alumina in the micro scale by using low temperature nitrogen adsorption-desorption system, indicating that the specific surface area of the prepared γ-alumina nanoparticles is larger than that of the γ-alumina in the micro scale. Furthermore, micro- and meso-pores were observed for the if-alumina nanoparticles while only mesoporous structure was detected for the γ-alumina in the micro scale. These experimental results suggested that the self assembly behavior of the γ-alumina nanoparticles may be due to the selective adsorption ofdimethyl disulfide in the micropores of these nanoparticles to act as bridge linking the nanoparticles.
