Transition metal-nitrogen-carbon(M-N-C)as a promising substitute for the conventional noble metalbased catalyst still suffers from low activity and durability for oxygen reduction reaction(ORR)in proton exchange membr...Transition metal-nitrogen-carbon(M-N-C)as a promising substitute for the conventional noble metalbased catalyst still suffers from low activity and durability for oxygen reduction reaction(ORR)in proton exchange membrane fuel cells(PEMFCs).To tackle the issue,herein,a new type of sulfur-doped ironnitrogen-hard carbon(S-Fe-N-HC)nanosheets with high activity and durability in acid media were developed by using a newly synthesized precursor of amide-based polymer with Fe ions based on copolymerizing two monomers of 2,5-thiophene dicarboxylic acid(TDA)as S source and 1,8-diaminonaphthalene(DAN)as N source via an amination reaction.The as-synthesized S-Fe-N-HC features highly dispersed atomic Fe Nxmoieties embedded into rich thiophene-S doped hard carbon nanosheets filled with highly twisted graphite-like microcrystals,which is distinguished from the majority of M-N-C with soft or graphitic carbon structures.These unique characteristics endow S-Fe-N-HC with high ORR activity and outstanding durability in 0.5 M H_(2)SO_(4).Its initial half-wave potential is 0.80 V and the corresponding loss is only 21 m V after 30,000 cycles.Meanwhile,its practical PEMFC performance is a maximum power output of 628.0 mW cm^(-2)and a slight power density loss is 83.0 m W cm^(-2)after 200-cycle practical operation.Additionally,theoretical calculation shows that the activity of Fe Nxmoieties on ORR can be further enhanced by sulfur doping at meta-site near FeN_(4)C.These results evidently demonstrate that the dual effect of hard carbon substrate and S doping derived from the precursor platform of amid-polymers can effectively enhance the activity and durability of Fe-N-C catalysts,providing a new guidance for developing advanced M-N-C catalysts for ORR.展开更多
Dopamine polymerization reaction and hydrothermal method were used to prepare nickel coated Al_(2)O_(3)reinforcement phase(Ni/Al_(2)O_(3)).Ni/Al_(2)O_(3)reinforced Sn_(1.0)Ag_(0.5)Cu(SAC105)composite solder was prepar...Dopamine polymerization reaction and hydrothermal method were used to prepare nickel coated Al_(2)O_(3)reinforcement phase(Ni/Al_(2)O_(3)).Ni/Al_(2)O_(3)reinforced Sn_(1.0)Ag_(0.5)Cu(SAC105)composite solder was prepared using traditional casting method.The result shows that the nickel coating layer is continuous with uneven thickness.The interface between nickel and aluminum oxide exhibits a metallurgical bonding with coherent interface relationship.The strength,toughness and wettability of the SAC105 solder on the substrate are improved,while the conductivity is not decreased significantly.The fracture mode of composites transitions from a mixed toughness-brittleness mode to a purely toughness-dominated mode,characterized by many dimples.The prepared composite brazing material was made into solder paste for copper plate lap joint experiments.The maximum shear strength is achieved when the doping amount was 0.3wt%.The growth index of intermetallic compound at the brazing interface of Ni/Al_(2)O_(3)reinforced SAC105 composite solder is linearly fitted to n=0.39,demonstrating that the growth of intermetallic compound at the interface is a combined effect of grain boundary diffusion and bulk diffusion.展开更多
The aim of this study was to develop a novel pharmaceutical excipient:an anion exchange resin.Initially,polystyrenedivinylbenzene(PS-DVB)microspheres were synthesized via suspension polymerization.Subsequently,these m...The aim of this study was to develop a novel pharmaceutical excipient:an anion exchange resin.Initially,polystyrenedivinylbenzene(PS-DVB)microspheres were synthesized via suspension polymerization.Subsequently,these microspheres served as a substrate for chloromethylation using methanol,formaldehyde,and chlorosulfonic acid.By optimizing the reaction conditions,the chloromethylated microspheres were characterized using infrared spectroscopy,scanning electron microscopy,and the Mohr method.Under optimal reaction conditions,the resulting products exhibited uniformity and spherical morphology,with an average particle size of approximately 190μm.The PS-DVB microspheres effectively incorporated chloromethyl groups,as evidenced by a chlorine content of 14.67%.Scanning electron microscopy analysis indicated that the appearance of the microspheres remained largely unchanged post-reaction.Overall,the research findings demonstrated the successful preparation of the anion exchange resin.Characterization and quality assessment confirmed that the ion exchange resin met the required standards.展开更多
The penta-ether compound was synthesized by the reaction of di（trimethylolpropane） with sodium hydride as the strong base and methyl iodide as the alkyl halide. This compound was characterized by NMR, FTIR, and GC t...The penta-ether compound was synthesized by the reaction of di（trimethylolpropane） with sodium hydride as the strong base and methyl iodide as the alkyl halide. This compound was characterized by NMR, FTIR, and GC techniques. The MgCl_2-supported titanium catalysts were incorporated with varying amounts of penta-ether compound as the internal donor and also the catalysts without the internal donor were synthesized. The synthesized catalysts and the conventional ZieglerNatta catalyst were characterized. The titanium contents were determined by spectrophotometry, magnesium by complexometric titration and chloride by argentometric titration. The effects of the new internal donor on propylene polymerization with the prepared MgCl_2-supported Ziegler-Natta catalysts were investigated and then these results were compared to the results obtained using the conventional diisobutyl phthalate-besed-Ziegler-Natta catalyst. The highest crystallinity degree, melting temperature, and isotacticity of polypropylene were obtained using the catalyst with a pentaether/Mg molar ratio equal to 0.21.展开更多
The urethane reaction of o-hydroxybenzyl alcohol with phenyl isocyanate was monitored with in situ FT-IR.Dibutyltin dilaurate was used as catalyst and its amount effect was investigated.It was found that there was an ...The urethane reaction of o-hydroxybenzyl alcohol with phenyl isocyanate was monitored with in situ FT-IR.Dibutyltin dilaurate was used as catalyst and its amount effect was investigated.It was found that there was an obvious induction period before reaction began.It was interesting that the time of induction period climbed up and then declined with the increase of dibutyltin dilaurate. When the concentration of dibutyltin dilaurate reached 9.58×10^（-5） mol/L,the induction period disappeared completely and hereafter did not appear any more.Furthermore,the urethane reaction kinetics was studied.When the concentration of dibutyltin dilaurate increased,the reaction rate of phenolic group（k_1） increased sharply,but the reaction rate of alcoholic group（k_2） appeared of little change on the whole.k_1 increased about 20-fold,yet k_2 increased about 2-fold when the concentration of dibutyltin dilaurate varied from 9.58×10^（-6） mol/L to 1.92×10~4 mol/L,which made the value of k_1/k_2 enlarge.展开更多
Calcium acrylate is a polymerized grout, and can polymerize in an aqueous solution. The polymerization reaction utilizes ammonium persulfate as a catalyst and sodium thiosulfate as the activator. Based on the theory o...Calcium acrylate is a polymerized grout, and can polymerize in an aqueous solution. The polymerization reaction utilizes ammonium persulfate as a catalyst and sodium thiosulfate as the activator. Based on the theory of reaction kinetics, this study on the relation between gel time and concentration of activator and catalyst showed that gel time of calcium acrylate is inversely proportional to activator and catalyst concentration. A formula of gel time is proposed, and an example is provided to verify the proposed formula.展开更多
Based on the technology of titanium dioxide grafting modification withpolystyrene (PS), the modification mechanisms are studied and the polystyrene-grafting states on thesurface of titanium dioxide have been set up. U...Based on the technology of titanium dioxide grafting modification withpolystyrene (PS), the modification mechanisms are studied and the polystyrene-grafting states on thesurface of titanium dioxide have been set up. Under the synergistic actions of mechanical force,chemistry and heat, macromolecular free radicals of PS are created, at the same time, the O-O bondsof titanium dioxide are broken and the oxide free radicals produced, and the numbers of oxygen atomare increased and crystal lattice defects rich electrons are formed on the surface of titaniumdioxide. The radical polymerization is the main reaction between PS and titanium dioxide and C-Obonds form in the process of modification. Multi-sites chemical adsorption also exists besidesgrafting between PS and titanium dioxide.展开更多
Two distinct copper coordination polymers, namely [Cu^Ⅱ2（2,5-pydc）2（bpp）2]·H2O（1） and Cu2^ⅠCu^Ⅱ（2,5-pydc）2（bpp）2（2）（2,5-pydc = pyridine-2,5-dicarboxylic acid, bpp = 1,3-bi（4-pyridyl）propane）, h...Two distinct copper coordination polymers, namely [Cu^Ⅱ2（2,5-pydc）2（bpp）2]·H2O（1） and Cu2^ⅠCu^Ⅱ（2,5-pydc）2（bpp）2（2）（2,5-pydc = pyridine-2,5-dicarboxylic acid, bpp = 1,3-bi（4-pyridyl）propane）, have been successfully synthesized through hydrothermal conditions under different temperatures. Single-crystal X-ray structural analysis revealed that both complexes 1 and 2 are 3D frameworks. Complex 1 is an 8-connected 2-fold interpenetrating network based on [Cu（2,5-pydc）]4 molecular building block（MBB）, and also can be simplified as a 4-connected net if the Cu（Ⅱ） ion is regarded as an independent node, whereas 2 shows a（4,4）-connected non-interpenetrated framework which contains mixed valence Cu（Ⅰ/Ⅱ） centers. The results demonstrate that temperature plays a significant role in the final structures of the complexes.展开更多
Two novel complexes, namely {[Cd（AIP）（4,4＇-bpy）]·1.3DMF}n（1） and [Cd（AIP）（2,2＇- bpy）]n（2）, have been synthesized through solvothermal reaction（H2AIP = 5-aminoisophthalic acid, 2,2＇-bpy = 2,2＇-bip...Two novel complexes, namely {[Cd（AIP）（4,4＇-bpy）]·1.3DMF}n（1） and [Cd（AIP）（2,2＇- bpy）]n（2）, have been synthesized through solvothermal reaction（H2AIP = 5-aminoisophthalic acid, 2,2＇-bpy = 2,2＇-bipyridine, 4,4＇-bpy = 4,4＇-bipyridine, and DMF = N,N＇-dimethylformamide） and structurally determined by single-crystal X-ray diffraction. Complex 1 shows a three-dimensional（3D） layer-pillar framework with rectangular channels, while complex 2 displays a two-dimensional（2D） wave net architecture. Furthermore, 1 and 2 were characterized by elemental analysis, infrared spectra（IR）, thermal gravimetric analyses（TGA） and fluorescence measurements. The luminescent properties of 1 dispersed in various organic solvents have been investigated systematically, demonstrating high selectivity for acetone via the fluorescence quenching effect.展开更多
As emerging carbon-based nanoparticles,carbon dots(CDs)have attracted widespread attention in recent decades.Among the large family of CDs,carbonized polymer dots(CPDs)exhibit amazing charm due to their unique highly ...As emerging carbon-based nanoparticles,carbon dots(CDs)have attracted widespread attention in recent decades.Among the large family of CDs,carbonized polymer dots(CPDs)exhibit amazing charm due to their unique highly functionalized structure and typical polymeric characteristics.The polymerization and crosslinking of precursors during the synthesis process lead to the formation of a distinctive core-shell structure in CPDs,which consists of a hydrophobic carbon core and a polymer shell layer with entangled chain segments.In previous research,CPDs have been highlighted from the perspective of their outstanding photoluminescence properties.However,few discussions or summaries are available concerning the polymeric characteristics of CPDs.Herein,we try to provide a detailed discussion of the typical polymeric characteristics of CPDs and related applications.We first make an introduction to CPD synthesis in terms of the formation process,synthetic methods,and precursor varieties.Subsequently,we give a summary of several typical polymeric characteristics of CPDs and relevant characterization techniques.Furthermore,we list various applications of CPDs related to polymer characteristics,including sensing,optoelectronic devices,anti-counterfeiting,and so on.Finally,we put forward some reflections and perspectives for the development of CPDs.展开更多
基金finically supported by the National Natural Science Foundation of China(22075055)the Guangxi Science and Technology Project(AB16380030)。
文摘Transition metal-nitrogen-carbon(M-N-C)as a promising substitute for the conventional noble metalbased catalyst still suffers from low activity and durability for oxygen reduction reaction(ORR)in proton exchange membrane fuel cells(PEMFCs).To tackle the issue,herein,a new type of sulfur-doped ironnitrogen-hard carbon(S-Fe-N-HC)nanosheets with high activity and durability in acid media were developed by using a newly synthesized precursor of amide-based polymer with Fe ions based on copolymerizing two monomers of 2,5-thiophene dicarboxylic acid(TDA)as S source and 1,8-diaminonaphthalene(DAN)as N source via an amination reaction.The as-synthesized S-Fe-N-HC features highly dispersed atomic Fe Nxmoieties embedded into rich thiophene-S doped hard carbon nanosheets filled with highly twisted graphite-like microcrystals,which is distinguished from the majority of M-N-C with soft or graphitic carbon structures.These unique characteristics endow S-Fe-N-HC with high ORR activity and outstanding durability in 0.5 M H_(2)SO_(4).Its initial half-wave potential is 0.80 V and the corresponding loss is only 21 m V after 30,000 cycles.Meanwhile,its practical PEMFC performance is a maximum power output of 628.0 mW cm^(-2)and a slight power density loss is 83.0 m W cm^(-2)after 200-cycle practical operation.Additionally,theoretical calculation shows that the activity of Fe Nxmoieties on ORR can be further enhanced by sulfur doping at meta-site near FeN_(4)C.These results evidently demonstrate that the dual effect of hard carbon substrate and S doping derived from the precursor platform of amid-polymers can effectively enhance the activity and durability of Fe-N-C catalysts,providing a new guidance for developing advanced M-N-C catalysts for ORR.
基金ational Natural Science Foundation of China(U1604132)Central Plains Talents Program-Fund of Central Plains Leading Talents(ZYYCYU002130)+1 种基金Key Technology Research and Development Program of Henan Province(222102230114)Major Scientific Research Foundation of Higher Education of Henan Province(23B430003)。
文摘Dopamine polymerization reaction and hydrothermal method were used to prepare nickel coated Al_(2)O_(3)reinforcement phase(Ni/Al_(2)O_(3)).Ni/Al_(2)O_(3)reinforced Sn_(1.0)Ag_(0.5)Cu(SAC105)composite solder was prepared using traditional casting method.The result shows that the nickel coating layer is continuous with uneven thickness.The interface between nickel and aluminum oxide exhibits a metallurgical bonding with coherent interface relationship.The strength,toughness and wettability of the SAC105 solder on the substrate are improved,while the conductivity is not decreased significantly.The fracture mode of composites transitions from a mixed toughness-brittleness mode to a purely toughness-dominated mode,characterized by many dimples.The prepared composite brazing material was made into solder paste for copper plate lap joint experiments.The maximum shear strength is achieved when the doping amount was 0.3wt%.The growth index of intermetallic compound at the brazing interface of Ni/Al_(2)O_(3)reinforced SAC105 composite solder is linearly fitted to n=0.39,demonstrating that the growth of intermetallic compound at the interface is a combined effect of grain boundary diffusion and bulk diffusion.
基金2023 Nantong Jianghai Talents Project,the Nantong Social Livelihood Science and Technology Plan for 2023the 2022 New Drugs and Platform Enhancement Project of the Yangtze Delta Drug Advanced Research Institute.Additionally,support was provided by the Zhenjiang Science and Technology Project(Grant No.SH2020048)+2 种基金the China Postdoctoral Science Foundation(Grant No.2020M681532)the Jiangsu Planned Projects for Postdoctoral Research Funds(Grant No.2020Z209)the Natural Science Research Projects of Universities in Jiangsu Province(Grant No.20KJD350001).
文摘The aim of this study was to develop a novel pharmaceutical excipient:an anion exchange resin.Initially,polystyrenedivinylbenzene(PS-DVB)microspheres were synthesized via suspension polymerization.Subsequently,these microspheres served as a substrate for chloromethylation using methanol,formaldehyde,and chlorosulfonic acid.By optimizing the reaction conditions,the chloromethylated microspheres were characterized using infrared spectroscopy,scanning electron microscopy,and the Mohr method.Under optimal reaction conditions,the resulting products exhibited uniformity and spherical morphology,with an average particle size of approximately 190μm.The PS-DVB microspheres effectively incorporated chloromethyl groups,as evidenced by a chlorine content of 14.67%.Scanning electron microscopy analysis indicated that the appearance of the microspheres remained largely unchanged post-reaction.Overall,the research findings demonstrated the successful preparation of the anion exchange resin.Characterization and quality assessment confirmed that the ion exchange resin met the required standards.
基金financially supported by the Marun Petrochemical Co.,Mahshahr,Iran
文摘The penta-ether compound was synthesized by the reaction of di（trimethylolpropane） with sodium hydride as the strong base and methyl iodide as the alkyl halide. This compound was characterized by NMR, FTIR, and GC techniques. The MgCl_2-supported titanium catalysts were incorporated with varying amounts of penta-ether compound as the internal donor and also the catalysts without the internal donor were synthesized. The synthesized catalysts and the conventional ZieglerNatta catalyst were characterized. The titanium contents were determined by spectrophotometry, magnesium by complexometric titration and chloride by argentometric titration. The effects of the new internal donor on propylene polymerization with the prepared MgCl_2-supported Ziegler-Natta catalysts were investigated and then these results were compared to the results obtained using the conventional diisobutyl phthalate-besed-Ziegler-Natta catalyst. The highest crystallinity degree, melting temperature, and isotacticity of polypropylene were obtained using the catalyst with a pentaether/Mg molar ratio equal to 0.21.
基金supported by the National Natural Science Foundation of China(No20676074 and No21176147)
文摘The urethane reaction of o-hydroxybenzyl alcohol with phenyl isocyanate was monitored with in situ FT-IR.Dibutyltin dilaurate was used as catalyst and its amount effect was investigated.It was found that there was an obvious induction period before reaction began.It was interesting that the time of induction period climbed up and then declined with the increase of dibutyltin dilaurate. When the concentration of dibutyltin dilaurate reached 9.58×10^（-5） mol/L,the induction period disappeared completely and hereafter did not appear any more.Furthermore,the urethane reaction kinetics was studied.When the concentration of dibutyltin dilaurate increased,the reaction rate of phenolic group（k_1） increased sharply,but the reaction rate of alcoholic group（k_2） appeared of little change on the whole.k_1 increased about 20-fold,yet k_2 increased about 2-fold when the concentration of dibutyltin dilaurate varied from 9.58×10^（-6） mol/L to 1.92×10~4 mol/L,which made the value of k_1/k_2 enlarge.
文摘Calcium acrylate is a polymerized grout, and can polymerize in an aqueous solution. The polymerization reaction utilizes ammonium persulfate as a catalyst and sodium thiosulfate as the activator. Based on the theory of reaction kinetics, this study on the relation between gel time and concentration of activator and catalyst showed that gel time of calcium acrylate is inversely proportional to activator and catalyst concentration. A formula of gel time is proposed, and an example is provided to verify the proposed formula.
文摘Based on the technology of titanium dioxide grafting modification withpolystyrene (PS), the modification mechanisms are studied and the polystyrene-grafting states on thesurface of titanium dioxide have been set up. Under the synergistic actions of mechanical force,chemistry and heat, macromolecular free radicals of PS are created, at the same time, the O-O bondsof titanium dioxide are broken and the oxide free radicals produced, and the numbers of oxygen atomare increased and crystal lattice defects rich electrons are formed on the surface of titaniumdioxide. The radical polymerization is the main reaction between PS and titanium dioxide and C-Obonds form in the process of modification. Multi-sites chemical adsorption also exists besidesgrafting between PS and titanium dioxide.
基金supported by the application basis research key project of Yunnan Province science and technology department(201401CB00299)the major project of Qujing Normal University(2012ZD002)
文摘Two distinct copper coordination polymers, namely [Cu^Ⅱ2（2,5-pydc）2（bpp）2]·H2O（1） and Cu2^ⅠCu^Ⅱ（2,5-pydc）2（bpp）2（2）（2,5-pydc = pyridine-2,5-dicarboxylic acid, bpp = 1,3-bi（4-pyridyl）propane）, have been successfully synthesized through hydrothermal conditions under different temperatures. Single-crystal X-ray structural analysis revealed that both complexes 1 and 2 are 3D frameworks. Complex 1 is an 8-connected 2-fold interpenetrating network based on [Cu（2,5-pydc）]4 molecular building block（MBB）, and also can be simplified as a 4-connected net if the Cu（Ⅱ） ion is regarded as an independent node, whereas 2 shows a（4,4）-connected non-interpenetrated framework which contains mixed valence Cu（Ⅰ/Ⅱ） centers. The results demonstrate that temperature plays a significant role in the final structures of the complexes.
基金the National Natural Science Foundation of China(21501178)Natural Science Funds of Fujian Province(No.2014H0055)for financial support of this work
文摘Two novel complexes, namely {[Cd（AIP）（4,4＇-bpy）]·1.3DMF}n（1） and [Cd（AIP）（2,2＇- bpy）]n（2）, have been synthesized through solvothermal reaction（H2AIP = 5-aminoisophthalic acid, 2,2＇-bpy = 2,2＇-bipyridine, 4,4＇-bpy = 4,4＇-bipyridine, and DMF = N,N＇-dimethylformamide） and structurally determined by single-crystal X-ray diffraction. Complex 1 shows a three-dimensional（3D） layer-pillar framework with rectangular channels, while complex 2 displays a two-dimensional（2D） wave net architecture. Furthermore, 1 and 2 were characterized by elemental analysis, infrared spectra（IR）, thermal gravimetric analyses（TGA） and fluorescence measurements. The luminescent properties of 1 dispersed in various organic solvents have been investigated systematically, demonstrating high selectivity for acetone via the fluorescence quenching effect.
基金supported by the Natural Science Foundation of Jilin Province(no.202402011)the National Natural Science Foundation of China(NSFC)under Grant No.22035001.
文摘As emerging carbon-based nanoparticles,carbon dots(CDs)have attracted widespread attention in recent decades.Among the large family of CDs,carbonized polymer dots(CPDs)exhibit amazing charm due to their unique highly functionalized structure and typical polymeric characteristics.The polymerization and crosslinking of precursors during the synthesis process lead to the formation of a distinctive core-shell structure in CPDs,which consists of a hydrophobic carbon core and a polymer shell layer with entangled chain segments.In previous research,CPDs have been highlighted from the perspective of their outstanding photoluminescence properties.However,few discussions or summaries are available concerning the polymeric characteristics of CPDs.Herein,we try to provide a detailed discussion of the typical polymeric characteristics of CPDs and related applications.We first make an introduction to CPD synthesis in terms of the formation process,synthetic methods,and precursor varieties.Subsequently,we give a summary of several typical polymeric characteristics of CPDs and relevant characterization techniques.Furthermore,we list various applications of CPDs related to polymer characteristics,including sensing,optoelectronic devices,anti-counterfeiting,and so on.Finally,we put forward some reflections and perspectives for the development of CPDs.
