As one of the most stable metal-organtic framework(MOF),zeolitic imidazolate framework-8(ZIF-8)has been widely studied for applications in the field of energy storage,catalysis,and environment protection.In this paper...As one of the most stable metal-organtic framework(MOF),zeolitic imidazolate framework-8(ZIF-8)has been widely studied for applications in the field of energy storage,catalysis,and environment protection.In this paper,ZIF-8 was employed to enhance the electrochemical properties and thermal stability of the electrospun poly(vinylidene fluoride-co-hexafluoropropylene)/polyacrylonitrile(PVDF-HFP/PAN)composite separator.The results indicate that the test cells assembled with the composite separators show improved rate capability,high discharge capacity,and stable cycling performances.The addition of ZIF-8 can improve the affinity of PVDF-HFP/PAN toward liquid electrolytes,and further enhance the ionic conductivity of the composite separators.In addition,the thermal stability of the PVDF-HFP/PAN separator has been improved by ZIF-8 nanoparticles.This work can provide insight into the application of MOF materials in Li-ion batteries.展开更多
The efficient adsorption of radioactive iodine(^(129)I and^(131)I)as nuclear waste is of great importance.Polymer nanocomposites consist of metal-organic frameworks(MOFs)developing for various pollutions sorption and ...The efficient adsorption of radioactive iodine(^(129)I and^(131)I)as nuclear waste is of great importance.Polymer nanocomposites consist of metal-organic frameworks(MOFs)developing for various pollutions sorption and separation have attracted much attention.This study reports the fabrication of magnetic polyacrylonitrile(PAN)/zeolitic imidazolate frameworks(ZIF-8)nanocomposites,PAN/ZIF-8(x%)/Fe_(3)O_(4),x=30 and 50,as iodine capture adsorbents.The PAN/ZIF-8(x%)/Fe_(3)O_(4)nanocomposite beads were fabricated via the phase inversion method,and their potential for iodine capture and separation in solution and vapor was investigated through UV-vis and weighing methods,respectively.Also,antibacterial activity of the as-prepared beads was assessed against E.coil and S.aureus.The as-fabricated compounds were studied by various techniques such as Fourier-transform infrared,X-ray diffraction,scanning electron microscope,energy-dispersive X-ray spectroscopy mapping,transmission electron microscope,N_(2)adsorption isotherm,and vibrating sample magnetometer.The iodine capture results showed that the efficiency of nanocomposites is remarkably higher than the pure PAN beads.Additionally,the asprepared nanocomposite adsorbents displayed higher capture capacities for iodine vapor(1524-4345mg·g^(-1))than iodine solution(187-295 mg·g^(-1)).The as-obtained magnetic nanocomposites can be successfully separated from polluted media by simple filtration or an external magnet,regenerated through washing with ethanol,and reused.Fast capturing,high sorption capacity,rapid separation,and good reusability make the PAN/ZIF-8(x%)/Fe_(3)O_(4)nanocomposites highly effective adsorbents for the separation of iodine from wastewater.Additionally,PAN/ZIF-8(50%)/Fe_(3)O_(4)bead can be considered as a potential new antibacterial agent for water and wastewater treatment.展开更多
A novel carbon fiber pretreatment was proposed.Polyacrylonitrile(PAN)-based carbon fibers were first anodized in H3PO4 electrolyte to achieve an active surface,and then coated with Mo-B catalysts by immersed the carbo...A novel carbon fiber pretreatment was proposed.Polyacrylonitrile(PAN)-based carbon fibers were first anodized in H3PO4 electrolyte to achieve an active surface,and then coated with Mo-B catalysts by immersed the carbon fibers in a uniformly dispersed Mo-B sol.The as-treated carbon fibers were then graphitized at 2 400 ℃ for 2 h.The structural changes were characterized by X-ray diffractometry(XRD),Raman spectroscopy,scanning electron microscopy(SEM) and high-resolution transmission electronic microscopy(HRTEM).The results show that much better graphitization can be achieved in the presence of Mo-B,with an interlayer spacing(d002) of 0.335 8 nm and a crystalline size(Lc) of 28 nm.展开更多
In this study, the effect of combining different molecular domains on single platform has been reported that revealed a proper packing and interpenetration of fullerene spheres with the monomeric species. The fabricat...In this study, the effect of combining different molecular domains on single platform has been reported that revealed a proper packing and interpenetration of fullerene spheres with the monomeric species. The fabricated IPN system exhibits hydrophobic behavior in nature. An interpenetrating polymer network (IPN) of fullerene-based poly (methyl hydro siloxane) (PMHS) and polyacrylonitrile (PAN) was prepared. The synthesized polymer network was characterized using infrared (IR) spectroscopy, differential scanning calorimetric analysis (DSC), and scanning electron microscopic (SEM) technique. The IPN was analyzed by IR spectroscopy, which depicts presence of fullerene at 500 cm<sup>−1</sup> and 1632 cm<sup>−1</sup>, presence of PHMS at 1050 cm<sup>−1</sup>, 1250 cm<sup>−1</sup>, 2225 cm<sup>−1</sup>, and 3000 cm<sup>−1</sup> and presence of PAN at 3077 cm<sup>−1</sup>, 1299 cm<sup>−1</sup>, 1408 cm<sup>−1</sup> and 2083 cm<sup>−1</sup>. Shifting in band positions indicated the interpenetration of the reacting species. DSC endotherm showed crystalline peak (T<sub>c</sub>) at 117˚C, which indicated the crystalline nature of the synthesized IPN. The absence of T<sub>g</sub> peak and clear observable T<sub>c</sub> peak revealed crystalline behavior of polymeric network. The microstructure of the polymer network was observed by SEM technique, which revealed transparent and dual-phase morphology of the IPN surface. The fluorescent emission spectra of polymeric network were recorded on a spectrofluorometer which revealed fluorescent excitation and emission spectra of the IPN. The Emission spectra generated by radiative decay of excitations exhibit a maximal peak at 450 nm, suggesting that the synthesized IPN nanosheets were typically high-intensity blue light emitting materials. The FTIR investigations revealed multiple non-covalent interactions achieved by polymerization with physical anchoring on the polymeric network surfaces. Such interactions can be recognized as the driving force for the fabrication of hydrophobic flexible silicon-based materials with a self-cleansing action.展开更多
以SBA-15为硬模板剂,采用溶剂挥发诱导煤基沥青烯与聚丙烯腈(PAN)自组装,制备了氮掺杂有序介孔炭(NOMC)。通过CO_(2)活化,进一步提升NOMC的比表面积及电容性能。结果表明,SBA-15、沥青烯、PAN的比例为1∶1.2∶4.8时,800℃炭化所得炭材...以SBA-15为硬模板剂,采用溶剂挥发诱导煤基沥青烯与聚丙烯腈(PAN)自组装,制备了氮掺杂有序介孔炭(NOMC)。通过CO_(2)活化,进一步提升NOMC的比表面积及电容性能。结果表明,SBA-15、沥青烯、PAN的比例为1∶1.2∶4.8时,800℃炭化所得炭材料成炭率与有序性均较高。900℃活化后其比表面积、孔容及孔径依次为602.1 m 2/g,0.426 cm 3/g,3.808 nm,且比电容达到127.2 F/g,相比未活化,提升了41.8%。展开更多
The process of electrodepositing Fe-Cr2O3 composite coating on polyacrylonitrile(PAN)-based carbon fibers and its catalytic graphitization were studied.Carbon fibers with and without electrodeposited Fe-Cr2O3 composit...The process of electrodepositing Fe-Cr2O3 composite coating on polyacrylonitrile(PAN)-based carbon fibers and its catalytic graphitization were studied.Carbon fibers with and without electrodeposited Fe-Cr2O3 composite coating were heat treated at different temperatures and the structural changes were characterized by XRD,Raman spectroscopy and SEM.The results indicate that Fe-Cr2O3 composite coating exhibits a significant catalytic effect on graphitization of carbon fibers at low temperatures.When the Fe-Cr2O3-coated carbon fibers were heat treated at 1 300°C,the interlayer spacing(d002) and ratio of relative peak area(AD/AG) reach 3.364-and 0.34,respectively.Whereas,the extent of graphitization of pristine carbon fibers is comparatively low even after heat treatment at 2 800°C and the values of d002 and AD/AG are 3.414 and 0.68,respectively.The extent of graphitization of carbon fibers increases not only with the increase of the catalyst gross but also the Cr2O3 content in Fe-Cr2O3 coating.The catalytic effect of Fe-Cr2O3 composite coating accords with the dissolution precipitation mechanism.展开更多
The Birimian Baguiomo formations are located in the northern part of the Boromo greenstone belt. In this belt, the volcanic rocks (tholeiitic basalt, calcalkaline basalt, andesite) hosting the gold mineralization are ...The Birimian Baguiomo formations are located in the northern part of the Boromo greenstone belt. In this belt, the volcanic rocks (tholeiitic basalt, calcalkaline basalt, andesite) hosting the gold mineralization are located in the Kwademen-Baguiomo shear zone. This mineralization, located only a few kilometers from the Kwademen gold deposit, is uncharacterized and, together with the latter, could constitute a gold potential capable of being economically exploitable. It is in this sense that this work is carried out with a view to characterizing the gold mineralization of the Baguiomo gold panning site. To carry out this work, we have made direct field measurements, combined with microstructures, and combined all this with data from geochemical rock analysis of the basalts that are the main host formations. Geochemical data show that tholeitic basalts formed from a mantle plume that was emplaced in an oceanic plateau context. Calc-alkaline basalts and andesites are comparable to Paleoproterozoic tholeitic basalts (PTH3), which are slightly enriched in light rare earths. Fertility tests show that these basalts concentrate between 3 and 6 ppb of gold at the time of accretion, which is sufficient for remobilization of this primary gold during the Eburnian orogeny to yield a deposit of around 4 - 5 Moz. Gold mineralization is associated with pyrite crystals when the latter are disseminated in the rock mass, whereas it is associated with hematite in quartz veins concordant with S1 shear deformation. It is mainly the pyrite crystals in the pressure shadows that contain the gold grains, whose development would be synchronous with micro-shear zone reactivation during the first phase of D1<sub>B</sub> deformation. The second phase of D2<sub>B</sub> deformation, which is a crenulation or fracture schistosity, does not significantly affect the shear deformation that controls mineralization.展开更多
基金supported by National Natural Science Foundation of China(12002295)Key Scientific Research Project of Education Department of Hunan Province,Xiangtan City,China(22A0113)Major Science and Technology Projects of Xiangtan Science and Technology Bureau(GX-ZD202210011).
文摘As one of the most stable metal-organtic framework(MOF),zeolitic imidazolate framework-8(ZIF-8)has been widely studied for applications in the field of energy storage,catalysis,and environment protection.In this paper,ZIF-8 was employed to enhance the electrochemical properties and thermal stability of the electrospun poly(vinylidene fluoride-co-hexafluoropropylene)/polyacrylonitrile(PVDF-HFP/PAN)composite separator.The results indicate that the test cells assembled with the composite separators show improved rate capability,high discharge capacity,and stable cycling performances.The addition of ZIF-8 can improve the affinity of PVDF-HFP/PAN toward liquid electrolytes,and further enhance the ionic conductivity of the composite separators.In addition,the thermal stability of the PVDF-HFP/PAN separator has been improved by ZIF-8 nanoparticles.This work can provide insight into the application of MOF materials in Li-ion batteries.
基金financial support(SCU.SC1400.29011)from the Shahid Chamran University of Ahvaz。
文摘The efficient adsorption of radioactive iodine(^(129)I and^(131)I)as nuclear waste is of great importance.Polymer nanocomposites consist of metal-organic frameworks(MOFs)developing for various pollutions sorption and separation have attracted much attention.This study reports the fabrication of magnetic polyacrylonitrile(PAN)/zeolitic imidazolate frameworks(ZIF-8)nanocomposites,PAN/ZIF-8(x%)/Fe_(3)O_(4),x=30 and 50,as iodine capture adsorbents.The PAN/ZIF-8(x%)/Fe_(3)O_(4)nanocomposite beads were fabricated via the phase inversion method,and their potential for iodine capture and separation in solution and vapor was investigated through UV-vis and weighing methods,respectively.Also,antibacterial activity of the as-prepared beads was assessed against E.coil and S.aureus.The as-fabricated compounds were studied by various techniques such as Fourier-transform infrared,X-ray diffraction,scanning electron microscope,energy-dispersive X-ray spectroscopy mapping,transmission electron microscope,N_(2)adsorption isotherm,and vibrating sample magnetometer.The iodine capture results showed that the efficiency of nanocomposites is remarkably higher than the pure PAN beads.Additionally,the asprepared nanocomposite adsorbents displayed higher capture capacities for iodine vapor(1524-4345mg·g^(-1))than iodine solution(187-295 mg·g^(-1)).The as-obtained magnetic nanocomposites can be successfully separated from polluted media by simple filtration or an external magnet,regenerated through washing with ethanol,and reused.Fast capturing,high sorption capacity,rapid separation,and good reusability make the PAN/ZIF-8(x%)/Fe_(3)O_(4)nanocomposites highly effective adsorbents for the separation of iodine from wastewater.Additionally,PAN/ZIF-8(50%)/Fe_(3)O_(4)bead can be considered as a potential new antibacterial agent for water and wastewater treatment.
基金Project(2006CB600903) supported by the National Basic Research Program of China
文摘A novel carbon fiber pretreatment was proposed.Polyacrylonitrile(PAN)-based carbon fibers were first anodized in H3PO4 electrolyte to achieve an active surface,and then coated with Mo-B catalysts by immersed the carbon fibers in a uniformly dispersed Mo-B sol.The as-treated carbon fibers were then graphitized at 2 400 ℃ for 2 h.The structural changes were characterized by X-ray diffractometry(XRD),Raman spectroscopy,scanning electron microscopy(SEM) and high-resolution transmission electronic microscopy(HRTEM).The results show that much better graphitization can be achieved in the presence of Mo-B,with an interlayer spacing(d002) of 0.335 8 nm and a crystalline size(Lc) of 28 nm.
文摘In this study, the effect of combining different molecular domains on single platform has been reported that revealed a proper packing and interpenetration of fullerene spheres with the monomeric species. The fabricated IPN system exhibits hydrophobic behavior in nature. An interpenetrating polymer network (IPN) of fullerene-based poly (methyl hydro siloxane) (PMHS) and polyacrylonitrile (PAN) was prepared. The synthesized polymer network was characterized using infrared (IR) spectroscopy, differential scanning calorimetric analysis (DSC), and scanning electron microscopic (SEM) technique. The IPN was analyzed by IR spectroscopy, which depicts presence of fullerene at 500 cm<sup>−1</sup> and 1632 cm<sup>−1</sup>, presence of PHMS at 1050 cm<sup>−1</sup>, 1250 cm<sup>−1</sup>, 2225 cm<sup>−1</sup>, and 3000 cm<sup>−1</sup> and presence of PAN at 3077 cm<sup>−1</sup>, 1299 cm<sup>−1</sup>, 1408 cm<sup>−1</sup> and 2083 cm<sup>−1</sup>. Shifting in band positions indicated the interpenetration of the reacting species. DSC endotherm showed crystalline peak (T<sub>c</sub>) at 117˚C, which indicated the crystalline nature of the synthesized IPN. The absence of T<sub>g</sub> peak and clear observable T<sub>c</sub> peak revealed crystalline behavior of polymeric network. The microstructure of the polymer network was observed by SEM technique, which revealed transparent and dual-phase morphology of the IPN surface. The fluorescent emission spectra of polymeric network were recorded on a spectrofluorometer which revealed fluorescent excitation and emission spectra of the IPN. The Emission spectra generated by radiative decay of excitations exhibit a maximal peak at 450 nm, suggesting that the synthesized IPN nanosheets were typically high-intensity blue light emitting materials. The FTIR investigations revealed multiple non-covalent interactions achieved by polymerization with physical anchoring on the polymeric network surfaces. Such interactions can be recognized as the driving force for the fabrication of hydrophobic flexible silicon-based materials with a self-cleansing action.
文摘以SBA-15为硬模板剂,采用溶剂挥发诱导煤基沥青烯与聚丙烯腈(PAN)自组装,制备了氮掺杂有序介孔炭(NOMC)。通过CO_(2)活化,进一步提升NOMC的比表面积及电容性能。结果表明,SBA-15、沥青烯、PAN的比例为1∶1.2∶4.8时,800℃炭化所得炭材料成炭率与有序性均较高。900℃活化后其比表面积、孔容及孔径依次为602.1 m 2/g,0.426 cm 3/g,3.808 nm,且比电容达到127.2 F/g,相比未活化,提升了41.8%。
基金Project(2006CB600903) supported by the National Basic Research Program of China
文摘The process of electrodepositing Fe-Cr2O3 composite coating on polyacrylonitrile(PAN)-based carbon fibers and its catalytic graphitization were studied.Carbon fibers with and without electrodeposited Fe-Cr2O3 composite coating were heat treated at different temperatures and the structural changes were characterized by XRD,Raman spectroscopy and SEM.The results indicate that Fe-Cr2O3 composite coating exhibits a significant catalytic effect on graphitization of carbon fibers at low temperatures.When the Fe-Cr2O3-coated carbon fibers were heat treated at 1 300°C,the interlayer spacing(d002) and ratio of relative peak area(AD/AG) reach 3.364-and 0.34,respectively.Whereas,the extent of graphitization of pristine carbon fibers is comparatively low even after heat treatment at 2 800°C and the values of d002 and AD/AG are 3.414 and 0.68,respectively.The extent of graphitization of carbon fibers increases not only with the increase of the catalyst gross but also the Cr2O3 content in Fe-Cr2O3 coating.The catalytic effect of Fe-Cr2O3 composite coating accords with the dissolution precipitation mechanism.
文摘The Birimian Baguiomo formations are located in the northern part of the Boromo greenstone belt. In this belt, the volcanic rocks (tholeiitic basalt, calcalkaline basalt, andesite) hosting the gold mineralization are located in the Kwademen-Baguiomo shear zone. This mineralization, located only a few kilometers from the Kwademen gold deposit, is uncharacterized and, together with the latter, could constitute a gold potential capable of being economically exploitable. It is in this sense that this work is carried out with a view to characterizing the gold mineralization of the Baguiomo gold panning site. To carry out this work, we have made direct field measurements, combined with microstructures, and combined all this with data from geochemical rock analysis of the basalts that are the main host formations. Geochemical data show that tholeitic basalts formed from a mantle plume that was emplaced in an oceanic plateau context. Calc-alkaline basalts and andesites are comparable to Paleoproterozoic tholeitic basalts (PTH3), which are slightly enriched in light rare earths. Fertility tests show that these basalts concentrate between 3 and 6 ppb of gold at the time of accretion, which is sufficient for remobilization of this primary gold during the Eburnian orogeny to yield a deposit of around 4 - 5 Moz. Gold mineralization is associated with pyrite crystals when the latter are disseminated in the rock mass, whereas it is associated with hematite in quartz veins concordant with S1 shear deformation. It is mainly the pyrite crystals in the pressure shadows that contain the gold grains, whose development would be synchronous with micro-shear zone reactivation during the first phase of D1<sub>B</sub> deformation. The second phase of D2<sub>B</sub> deformation, which is a crenulation or fracture schistosity, does not significantly affect the shear deformation that controls mineralization.
