期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
不同表面活性剂修饰的钯-镍双金属电极的制备与性能表征 被引量:2
1
作者 孙治荣 韩延波 +2 位作者 王坤 高明 仝杉 《应用基础与工程科学学报》 EI CSCD 北大核心 2012年第6期1072-1080,共9页
采用电沉积法分别制备以钛网(Ti)为基体材料的聚吡咯(PPy)修饰的、PPy与十六烷基三甲基溴化铵(CTAB)、PPy与十二烷基硫酸钠(SDS)、PPy与十二烷基磺酸钠(SLS)联合修饰的钯-镍双金属(Pd-Ni)催化电极(Pd-Ni/PPy/Ti电极、Pd-Ni(CTAB)/PPy/T... 采用电沉积法分别制备以钛网(Ti)为基体材料的聚吡咯(PPy)修饰的、PPy与十六烷基三甲基溴化铵(CTAB)、PPy与十二烷基硫酸钠(SDS)、PPy与十二烷基磺酸钠(SLS)联合修饰的钯-镍双金属(Pd-Ni)催化电极(Pd-Ni/PPy/Ti电极、Pd-Ni(CTAB)/PPy/Ti电极、Pd-Ni(SDS)/PPy/Ti电极和Pd-Ni(SLS)/PPy/Ti电极).探讨了不同表面活性剂掺杂对电极电化学催化活性的影响.循环伏安(CV)测试表明,在研究范围内,4个电极的最大氢吸附峰电流值分别为-93、-116、-70、-82mA,Pd-Ni(CTAB)/PPy/Ti电极的电催化性能最优.扫描电镜(SEM)分析了不同表面活性剂的引入对电极表面形态的影响.利用电感耦合等离子体-原子发射光谱(ICP-AES)分析了电极表面Pd、Ni的负载量.X射线衍射(XRD)测试结果表明4电极都形成了钯镍合金.试验表明,阳离子表面活性剂CTAB的引入使电极具有很好的电催化性能,电化学脱氯潜能大. 展开更多
关键词 聚吡咯 钯-镍双金属 表面活性剂 电化学性能
下载PDF
聚吡咯与十二烷基苯磺酸钠修饰的钯-镍双金属电极的制备与性能表征
2
作者 孙治荣 韩延波 +1 位作者 高明 彭永臻 《北京工业大学学报》 CAS CSCD 北大核心 2013年第1期109-115,共7页
采用电沉积法,以钛(Ti)网为基体材料,分别用聚吡咯(PPy)修饰、PPy与十二烷基苯磺酸钠(SDBS)联合修饰,制备了钯-镍(Pd-Ni)双金属催化电极(Pd-Ni/PPy/Ti电极和Pd-Ni(SDBS)/PPy/Ti电极),探讨了SDBS掺杂对电极电化学催化活性的影响.循环伏安... 采用电沉积法,以钛(Ti)网为基体材料,分别用聚吡咯(PPy)修饰、PPy与十二烷基苯磺酸钠(SDBS)联合修饰,制备了钯-镍(Pd-Ni)双金属催化电极(Pd-Ni/PPy/Ti电极和Pd-Ni(SDBS)/PPy/Ti电极),探讨了SDBS掺杂对电极电化学催化活性的影响.循环伏安(CV)测试表明,在研究范围内,Pd-Ni/PPy/Ti电极的最大氢吸附峰电流值为-93 mA,Pd-Ni(SDBS)/PPy/Ti电极的最大氢吸附峰电流值为-154 mA,后者的电催化性能更优.用扫描电镜(SEM)观察了引入PPy和SDBS后电极表面形态的变化.利用电感耦合等离子体-原子发射光谱(ICP-AES)分析了电极表面Pd、Ni的负载量.X射线衍射(XRD)测试结果表明在2种电极上都形成了钯镍合金.实验表明,制备过程中引入表面活性剂SDBS,使Pd-Ni(SDBS)/PPy/Ti电极上的钯负载量减少,同时电催化性能提高,电化学脱氯潜能大. 展开更多
关键词 聚吡咯 十二烷基苯磺酸钠 钯-镍双金属 电化学性能
下载PDF
Selective suppression of toluene formation in solvent-free benzyl alcohol oxidation using supported Pd-Ni bimetallic nanoparticles 被引量:8
3
作者 Jianwei Che Mengjia Hao +4 位作者 Wuzhong Yi Hisayoshi Kobayashi Yuheng Zhou Liping Xiao Jie Fan 《Chinese Journal of Catalysis》 CSCD 北大核心 2017年第11期1870-1879,共10页
The solvent‐free oxidation of benzyl alcohol was studied using supported Pd‐Ni bimetallic nanoparticles.Compared with monometallic Pd,the addition of Ni to Pd was found to be effective in suppressing the nondesired ... The solvent‐free oxidation of benzyl alcohol was studied using supported Pd‐Ni bimetallic nanoparticles.Compared with monometallic Pd,the addition of Ni to Pd was found to be effective in suppressing the nondesired product toluene,thereby enhancing the selectivity towards benzaldehyde.This result was attributed to a dual effect of Ni addition:the weakening of dissociative adsorption of benzyl alcohol and the promotion of oxygen species involved in the oxidation pathway. 展开更多
关键词 Palladium‐nickel Bimetallic nanoparticle Benzyl alcohol TOLUENE Solvent‐free Oxidation
下载PDF
Bimetallic Pd-Ni core-shell nanoparticles catalysts for the Suzuki reaction 被引量:11
4
作者 Ji Xiang Peng Li Hanbao Chong Li Feng Fangyu Fu Zhuang Wang Shilin Zhang Manzhou Zhu 《Nano Research》 SCIE EI CAS CSCD 2014年第9期1337-1343,共7页
A simple and efficient solution-based method for the synthesis of Pd-Ni bimetallic nanoparticles (NPs) has been developed. A series of Pd-Ni bimetallic NPs were readily achieved by reduction of PdC12 and Ni(acac)2... A simple and efficient solution-based method for the synthesis of Pd-Ni bimetallic nanoparticles (NPs) has been developed. A series of Pd-Ni bimetallic NPs were readily achieved by reduction of PdC12 and Ni(acac)2 (acac = acetyl- acetonate) in the presence of oleylamine (OAm), oleic acid (OA) and benzyl alcohol. Furthermore, by using high-resolution transmission electron microscopy (HRTEM), energy-dispersive spectrometry (EDS) mapping and X-ray diffraction (XRD), we demonstrate that the as-prepared Pd-Ni bimetallic NPs have core-shell structures with a Pd-rich core and a Ni-rich shell. In addition, the as-obtained Pd-Ni bimetallic NPs with varying compositions show excellent catalytic activities in the Miyaura-Suzuki reaction. When the nickel molar percentage was 0.23 to 0.65, the conversion with the as-obtained Pd-Ni bimetallic catalysts was above 90%. It is believed that this strategy can be employed to produce a variety of other well-defined core-shell type multimetallic nanostructures. 展开更多
关键词 PD NI bimetallic NPs catalytic activities
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部