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991.
3种2-甲基-2-烷基-1,3-二硫杂环戊烷类化合物的合成 总被引:1,自引:0,他引:1
以对甲苯磺酸为催化剂, 3种酮类化合物和二硫代乙二醇在苯中共沸脱水,合成了 2 -甲基- 2 -乙基- 1, 3 -二硫杂环戊烷、2- 甲基- 2- 异丁基- 1, 3- 二硫杂环戊烷和 -2 -甲基- 2 -异戊基 1, 3 二硫杂环戊烷,产率分别为 71. 5%、74. 3%和 75. 6%,质量分数分别为 98 .8%、99. 1%和 98. 9%。经红外光谱分析、元素分析、核磁共振分析和色 -质联机分析确定了 3种产物的结构。 相似文献
992.
993.
首次将硫酸钾作为催化剂,引入到环氧丙基三乙基氯化铵中间体的合成反应中。与无催化剂体系相比,催化下的反应速率大幅度提高,反应时间显著缩短。以环氧氯丙烷的转化率和产物中环氧基保留率的乘积作为中间体性能的评价指标,通过正交实验优化出最佳条件:甲醇水溶液为溶剂,反应温度50℃、n(硫酸钾)∶n(环氧氯丙烷)=0.010、n(三乙胺)∶n(环氧氯丙烷)=1.0、反应时间为1.5 h。该条件下,环氧氯丙烷的转化率可达92.02%,产物中环氧基保留率达到70.67%。可见硫酸钾用于催化环氧丙基三乙基氯化铵的合成反应是适宜的。 相似文献
994.
利用环氧化苯乙烯-丁二烯-苯乙烯嵌段共聚物(ESBS)的环氧基与顺丁烯二酸氢钾(HKM)在相转移催化剂和开环催化剂存在的条件下开环反应制得钾离聚体。研究了其反应条件,由于添加了助剂BM,环氧基开环率达到了95.2%,并用FTIR确定了离聚体的生成;通过对不同环氧值ESBS开环反应,研究了不同离子基团质量摩尔浓度对离聚体物化性能的影响。 相似文献
995.
影响煤加氢液化反应的因素很多,不同的煤对氢敏感度不一样,有的容易加氢,有的不容易加氢.显然容易加氢的煤在经济上就比较划算.在煤的工业分析、元素分析和煤岩相显微组分含量分析的基础上,简要讨论了原料煤对煤液化的影响.在煤的组成和物理性质等与液化特征之间建立良好的对应关系,总结出适合煤液化用煤种的一些特性. 相似文献
996.
A prototype wind-powered reverse osmosis desalination system was constructed and tested on Coconut Island off the northern coast of Oahu, Hawaii, for brackish water desalination. The system has four major subsystems: a multi-vaned windmill/pump, a flow/pressure stabilizer, a reverse osmosis module, and a control mechanism. The feedback control mechanism, developed by this study, allowed this prototype system to be operated satisfactorily under mild ambient wind of 5 m/s or less. No auxiliary power source was needed. The system operational data showed that at an average wind speed of 5 m/s, brackish feedwater at a total dissolved solids concentration of 3000 mg/1 and at a flow rate of 13 1/min could be processed by this system. The average rejection rate of this prototype system was 97% and the average recovery ratio was 20%. The energy efficiency of the system was measured at 3 5%, which is comparable to the typical energy efficiency of well-operated multi-vaned windmills. Generally, the system's energy efficiency decreases as wind speed increases. 相似文献
997.
The linear and nonlinear shear rheological behaviors of poly(propylene) (PP)/clay (organophilic‐montmorillonite) nanocomposites (PP/org‐MMT) were investigated by an ARES rheometer. The materials were prepared by melt intercalation with maleic anhydride functionalized PP as a compatibilizer. The storage moduli (G′), loss moduli (G″), and dynamic viscosities of polymer/clay nanocomposites (PPCNs) increase monotonically with org‐MMT content. The presence of org‐MMT leads to pseudo‐solid‐like behaviors and slower relaxation behaviors of PPCN melts. For all samples, the dependence of G′ and G″ on ω shows nonterminal behaviors. At lower frequency, the steady shear viscosities of PPCNs increase with org‐MMT content. However, the PPCN melts show a greater shear thinning tendency than pure PP melt because of the preferential orientation of the MMT layers. Therefore, PPCNs have higher moduli but better processibility compared with pure PP.© 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2427–2434,2004 相似文献
998.
Jian Guo Li Fang Jiao HuaTang Yuan Li Qin Wang Hai Xia Li Ming Zhang Yong Mei Wang 《Electrochimica acta》2006,51(28):6275-6280
Layered Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 materials with x = 0, 0.01, 0.02, 0.03, 0.05 are prepared by a solid-state pyrolysis method. The oxide compounds were calcined with various Cr-doped contents, which result in greater difference in morphological (shape, particle size and specific surface area) and the electrochemical (first charge profile, reversible capacity and rate capability) differences. The Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 powders were characterized by means of X-ray diffraction (XRD), charge/discharge cycling, cyclic voltammetry, and SEM. XRD experiment revealed that the Li[Ni(1−x)/3Mn(1−x)/3Co(1−x)/3Crx]O2 (x = 0, 0.01, 0.02, 0.03, 0.05) were crystallized to well layered -NaFeO2 structure. The first specific discharge capacity and coulombic efficiency of the electrode of Cr-doped materials were higher than that of pristine material. When x = 0.02, the sample showed the highest first discharge capacity of 241.9 mAh g−1 at a current density of 30 mA g−1 in the voltage range 2.3–4.6 V, and the Cr-doped samples exhibited higher discharge capacity and better cycleability under medium and high current densities at room temperature. 相似文献
999.
1000.
Qing Mao Gongquan Sun Suli Wang Guoxiong Wang Aiwei Ye Yang Tian Qin Xin 《Electrochimica acta》2007,52(24):6763-6770
Catalyst-coated membrane (CCM) and catalyzed diffusion medium (CDM) prepared either by brush painting method or by spraying method were compared for direct methanol fuel cell (DMFC) anode and cathode. The pore structure and the morphology of the electrodes were characterized by mercury intrusion porosimetry (MIP) and scanning electron microscopy (SEM). Internal resistance corrected polarization curves were employed to separate the contribution of each compartment of the membrane electrode assembly (MEA) to the overall polarization. It was shown that the increased mass transport resistance in the anode diffusion layer made the anode in CDM form act as the methanol barrier. The CCM configuration and the increased pores in micron scales in the catalyst layer were in favor of improving the performance of both anode and cathode. Accounting for the effect of methanol permeation, the combination of the anode in CDM form prepared by brush painting method and the cathode in CCM form prepared by spraying method was finally selected as the optimized configuration for MEA, which had the highest DMFC performance under near-ambient conditions. 相似文献