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Alloying design and microstructural control strategies towards developing Mg alloys with enhanced ductility 被引量:10
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作者 Zhong-Zheng Jin Min Zha +4 位作者 Si-Qing wang shi-chao wang Cheng wang Hai-Long Jia Hui-Yuan wang 《Journal of Magnesium and Alloys》 SCIE EI CAS CSCD 2022年第5期1191-1206,共16页
Nowadays,magnesium(Mg)alloys are promising lightweight structural materials,especially in transportation and aerospace fields,due to their inherent low density and high specific strength.Most of the high-strength Mg a... Nowadays,magnesium(Mg)alloys are promising lightweight structural materials,especially in transportation and aerospace fields,due to their inherent low density and high specific strength.Most of the high-strength Mg alloys exhibit poor formability and ductility at room temperature,which limit their wide applications.However,by proper alloying design and/or delicate microstructural control,some newly developed Mg alloys,including rare-earth(RE)and RE-free ones,show enhanced ductility without significant loss of strength.To identify the critical reasons,recent researches on ductile Mg alloys have been reviewed from the aspects of alloying design strategies and microstructural control via advanced processing technologies.Moreover,some outlooks on enhanced ductility of Mg alloys are suggested,e.g.enhancing the beneficial effect of solute atoms,introducing second phase particles,tailoring bimodal-grained structures,introducing pre-twinning structures,etc.The current research progresses in alloying design and/or novel microstructural control have shed some lights on designing and producing Mg alloys with enhanced ductility. 展开更多
关键词 Mg alloys ALLOYING MICROSTRUCTURE DUCTILITY STRENGTH
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Facile fabrication of highly flexible,porous PEDOT:PSS/SWCNTs films for thermoelectric applications 被引量:2
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作者 Fu-Wei Liu Fei Zhong +7 位作者 shi-chao wang Wen-He Xie Xue Chen Ya-Ge Hu Yu-Ying Ge Yuan Gao Lei wang Zi-Qi Liang 《Chinese Physics B》 SCIE EI CAS CSCD 2022年第2期50-59,共10页
High-performance organic composite thermoelectric(TE)materials are considered as a promising alternative for harvesting heat energy.Herein,composite films of poly(3,4-ethyienedioxythiophene):poly(styrene sulfonate)/si... High-performance organic composite thermoelectric(TE)materials are considered as a promising alternative for harvesting heat energy.Herein,composite films of poly(3,4-ethyienedioxythiophene):poly(styrene sulfonate)/single-walled carbon nanotubes(PEDOT:PSS/SWCNTs)were fabricated by utilizing a convenient solution mixing method.Thereafter,the as-prepared hybrid films were treated using sulfuric acid(H_(2)SO_(4))to further optimize the TE performance.Film morphological studies revealed that the sulfuric acid treated PEDOT:PSS/SWCNTs composite samples all possessed porous structures.Due to the successful fabrication of highly conductive networks,the porous nano-architecture also exhibited much more excellent TE properties when compared with the dense structure of the pristine samples.For the post-treated sample,a high power factor of 156.43μW·m^(-1)·K^(-2)can be achieved by adjusting the content of CNTs,which is approximately 3 orders of magnitude higher than that of the corresponding untreated samples(0.23μW·m^(-1)·K^(-2)).Besides,the obtained films also showed excellent mechanical flexibility,owing to the porous nanostructure and the strong p–p interactions between the two components.This work indicates that the H_(2)SO_(4) treatment could be a promising strategy for fabricating highly-flexible and porous PEDOT:PSS/SWCNTs films with high TE performances. 展开更多
关键词 porous film thermoelectric properties FLEXIBILITY
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基于氧杂蒽结构的硫醚化合物的设计合成及引发/调控苯乙烯自由基聚合的研究
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作者 于昊宇 邵健为 +3 位作者 陈冬 王世超 王力 杨万泰 《高分子学报》 SCIE CAS CSCD 北大核心 2018年第11期1422-1429,共8页
讨论了5种含有氧杂蒽结构的硫醚化合物的合成过程.以占吨醇为起始原料,通过高氯酸催化其与苯硫酚缩合制备苯硫醚,通过对占吨醇氯代并与甲硫醇钠反应制备甲硫醚,2条路径最终均通过正丁基锂拔氢和烷基化反应得到目标产物.通过核磁共振(1H-... 讨论了5种含有氧杂蒽结构的硫醚化合物的合成过程.以占吨醇为起始原料,通过高氯酸催化其与苯硫酚缩合制备苯硫醚,通过对占吨醇氯代并与甲硫醇钠反应制备甲硫醚,2条路径最终均通过正丁基锂拔氢和烷基化反应得到目标产物.通过核磁共振(1H-NMR、13C-NMR)、傅里叶红外光谱(FTIR)和紫外可见吸收光谱(UV-Vis)手段对5种硫醚进行表征和结构确认.系统研究了硫醚化合物单独使用及其与传统引发剂共用时的苯乙烯(St)自由基聚合行为. 80°C下,硫醚化合物均能引发St的本体聚合,但聚合转化率低且表现出不受控的普通自由基聚合行为.而当将硫醚化合物与偶氮二异庚腈(ABVN)共同用于St在甲苯中的溶液聚合中时,能够在65°C下获得比本体聚合更高的转化率,聚合体系表现出一定的可控性,分子量随转化率增加呈现线性增长.此外,研究并对比了不同ABVN/硫醚化合物摩尔比和聚合温度下的St自由基聚合行为. 展开更多
关键词 可控自由基聚合 硫醚 苯乙烯 本体聚合 溶液聚合
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NiO nanoparticles-decorated ZnO hierarchical structures for isopropanol gas sensing 被引量:3
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作者 shi-chao wang Xiao-Hu wang +5 位作者 Gao-Qun Qiao Xiao-Yan Chen Xin-Zhen wang Nan-Nan Wu Jian Tian Hong-Zhi Cui 《Rare Metals》 SCIE EI CAS CSCD 2022年第3期960-971,共12页
In this paper,a three-dimensional(3D)hierar-chical ZnO structure consisting of nanosheets modified with ultrafine NiO particles was synthesized via a facile two-step chemical precipitate method.Various techniques char... In this paper,a three-dimensional(3D)hierar-chical ZnO structure consisting of nanosheets modified with ultrafine NiO particles was synthesized via a facile two-step chemical precipitate method.Various techniques characterized the as-synthesized ZnO/NiO composites and pure ZnO.The p-NiO/n-ZnO junctions formed between adjacent ZnO and NiO nanoparticles,improving the gas sensing performance.The ZnO/NiO composite with the Ni:Zn atomic ratio of 7.42:100 exhibited the best iso-propanol sensing properties.Compared to pure ZnO,it showed high selectivity and sensitivity(R_(a)/R_(g)=221.3 toward 400×10^(-6)isopropanol),fast response rate(less than 10 s),short recovery time,and simultaneously low operating temperature.Also,the ZnO/NiO composite exhibited a wide sensing range(1×10^(-6)-1000×10^(-6))to isopropanol and processed good long-term stability.The experimental results suggested the potential application in fabricating efficient isopropanol sensors using this ZnO/NiO composite.The enhanced isopropanol sensing mech-anism is also discussed in charge transfer between heterojunctions,surface area,and surface defects. 展开更多
关键词 ZNO NIO Hierarchical structure Gas sensor ISOPROPANOL
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Controlled Radical Polymerization of Styrene Mediated by Xanthene-9-thione and Its Derivatives 被引量:1
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作者 Hao-Yu Yu Jiao wang +4 位作者 Jian-Wei Shao Dong Chen shi-chao wang Li wang Wan-Tai Yang 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2018年第12期1303-1311,共9页
In our present work, a novel controlled radical polymerization system is developed based on xanthene-9-thione (XT). It was found that the radical polymerization of styrene (St) became controlled in the presence of... In our present work, a novel controlled radical polymerization system is developed based on xanthene-9-thione (XT). It was found that the radical polymerization of styrene (St) became controlled in the presence of a small amount of XT. At the early stage of the polymerization, the polymerization rate was relatively low and the as-formed polystyrene (PS) had low number-average molecular weight (Mn) and narrow polydispersity (D). After XT was consumed, the polymerization rate increased dramatically and the Mn of PS increased gradually with polymerization proceeding. When the polymerization of St was carried out with a proper molar ratio of initiator to XT and at an appropriate temperature, shortened slow polymerization stage and good control over Mn could be achieved. To further improve the regulating ability of XT, a series of substituent groups (-CF3, --CH(CH3)2, --N(CH3)2) were introduced onto the xanthene ring of XT, and the effects of these derivatives on the polymerization of St were investigated in detail. UV-Vis spectroscopy was carried out to monitor the concentration of XT during the polymerization and the chemical structure of the as-formed PS was fully characterized by IH- NMR and ESI-MS analysis. A possible mechanism involving the formation and evolution of the cross-termination products was proposed to interpret the observed polymerization behavior. 展开更多
关键词 Controlled radical polymerizaton Xanthene-9-thione STYRENE SUBSTITUENT ESI-MS
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Dual Palladium/Scandium Catalysis toward Rotationally Hindered C3-Naphthylated Indoles from β-Alkynyl Ketones and o-Alkynyl Anilines
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作者 Dan wang shi-chao wang +2 位作者 Wen-Juan Hao Shu-Jiang Tu Bo Jiang 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2021年第1期106-114,共9页
A new dual plldium/scandium catalysis starting fromβ-alkynyl ketones and o alkynyl anilines is reported for the first time,leading to the atom-economic synthesis of rotationally hindered C3-naphthylated indoles in mo... A new dual plldium/scandium catalysis starting fromβ-alkynyl ketones and o alkynyl anilines is reported for the first time,leading to the atom-economic synthesis of rotationally hindered C3-naphthylated indoles in moderate to good yields and high regioselectivi-ty.This method can tolerate normal air conditions,and features the use of palladium/scandium cooperative catalysts without any ligand,facile double annulation involving various internal alkynes,and good functional group tolerance. 展开更多
关键词 Dual metallic catalysis Regioselectivity BENZANNULATION Arylated indoles Internal alkynes
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