FeCo-based hybrid MOF derived active species for effective oxygen evolution

Metal-organic frameworks(MOFs) have been regarded as promising catalyst materials due to the richness of coordinately unsaturated metal sites on the surface,which can act as catalytic active centres.In this study,a hybrid MOF material composed of Fe-based MOF and Co-based MOF was prepared with the involvement of graphene oxide nanosheets as additive.It was demonstrated that the hybrid MOF materials showed much higher electro-catalytic activity towards oxygen evolution than the single-phase counterparts.To drive current density of 10 mA cm~(-2),the hybrid CoFe-based MOF only needed an over potential of 290 mV in 1 M KOH.The catalytic activity could sustain for a longer time with only slight current density decrease.During oxygen evolution operation,the MOF catalyst evolved into catalytic active species but kept well the microscale sheet-like structure.It is thus believed that this study will provide an avenue for the development of advanced electrocatalysts.     

Acyl-chloride functionalized graphene oxide chemically grafted with hindered phenol and its application in anti-degradation of polypropylene

In this study,graphene oxide (GO) nanosheets were first functionalized by the acyl-chloride reaction and then reacted with hindered phenol (HP) to obtain HP grafted GO (GO-g-HP).The GO-g-HP prepared under the optimized condition exhibited a high efficiency against both thermal and photo oxidation of isotactic polypropylene (iPP).GO-g-HP exhibited a much better anti-aging efficiency than that of HP and GO used individually or that of their physical mixture.The outstanding anti-aging effect of GO-g-HP was attributed to the excellent synergistic effect produced between the chemically bonded GO and HP,which resulted in an improved oxygen barrier property of GO and excellent utilization of the free radical scavenging capability of GO and HP.Also,thanks to the grafting of HP on GO,the physical loss of HP,which was one of the main shortcomings for traditional small molecular antioxidants,was largely suppressed.It is expected that the GO-g-HP prepared can well meet the requirement of long-term applications of polymers in some harsh service conditions.     

正交试验优化手性镍催化不对称反应条件研究

用正交试验法优化手性镍催化二乙基锌对α，β不饱和酮的不对称麦克尔加成反应条件，优化后的不对称麦克尔加成反应的一般条件为：低温(近反应溶剂冰点)，常压，非质子非极性溶剂(环己烷)．     

工程中常用的几种氧化沟及其发展

简要介绍了当今工程中常用的几种氧化沟技术的特点及其发展历程,主要包括Carrousel氧化沟、Orbal氧化沟、交替式氧化沟以及一体化氧化沟。     

pH、温度和浓度对苯酚在V掺杂MoOx-C/Ti电极上的电催化氧化的影响

采用溶胶-凝胶法合成MoOx、MoOx-V5 (x%)胶体,通过Vulcan XC-72炭黑负载制备炭载钼系氧化物电催化剂.利用循环伏安法(CV)测试手段研究苯酚在电极上的氧化降解,考察了掺杂元素、溶液pH值、苯酚浓度、扫描速率、温度对苯酚氧化性能的影响.测试结果表明:苯酚在电极上的氧化是受扩散和电子转移联合控制的复杂过程;掺杂过渡金属元素V可以降低苯酚氧化的表观活化能,提高电化学性能;溶液的pH值越低,MoOx-C/Ti电极对苯酚的催化氧化活性越高;pH在0～6,苯酚的氧化经历了相似的历程,包含了相同的电子数和质子数;苯酚氧化峰电流随着浓度、温度的增加而增加,到一定程度后趋于稳定.     

选择性催化氧化H2S的催化剂研究

在考察了几种单组分氧化物把硫化氢催化氧化为单质硫的基础上，采用共沉淀法合成了3种复合氧化物催化剂A，B，C，并考察了它们的催化活性和选择性．结果表明，在一定条件下，催化剂B的转化率和选择性分别在90％和97％以上，在40h的催化性能稳定性测试中，其转化率和选择性均能保持稳定，具有良好的催化性能．     

四苯基卟啉蒽醌化合物与钴(Ⅱ)配位反应动力学

用光度法研究了5-[p-(β-蒽醌酰亚胺)甲氧基]-10，15，20-对甲基四苯基卟啉(H2TPP)在DMF溶剂中与金属钴(Ⅱ)离子配位反应的动力学以及镉(Ⅱ)离子对该反应的催化作用，提出了反应机理，并研究了温度对反应动力学参数的影响，求得基元反应的活化参数△rHm^≠、△rSm^≠及平衡步的△rHm^θ、△rSm^θ．     

新型固体酸SO_4~(2-)MoO_3-TiO_2催化合成苹果酯

自制了一种新固体酸催化剂SO2 -4MoO3 -TiO2 ,FT -IR谱图表明 ,催化剂表面具有强酸中心 ,该催化剂对苹果酯合成的活性高 ,并得到该反应的优化条件如下 :乙酰乙酸乙酯 0 .3mol,乙二醇 0 .6mol,环己烷 30ml,催化剂 3g ,反应温度 110℃ ,反应时间 1.5h ,在此条件下 ,苹果酯产率达 90 % ,且催化剂易回收 ,具有较好的重复使用性能     

氨基磺酸均相催化合成柠檬酸三丁酯

以氨基磺酸为均相催化剂催化合成柠檬酸三丁酯,确定了酯化优化条件。试验结果表明:在催化剂6.0%(以柠檬酸为基数的质量百分数),柠檬酸0.1mol,丁醇0.55mol,反应温度100～150℃,反应时间90min的条件下,柠檬酸的酯化率达到98.6%以上。