高纯四溴双酚A双(2,3-二溴丙基)醚合成新工艺

研究了合成阻燃剂四溴双酚A双(2，3-二溴丙基)醚的新工艺，特点是通过加入表面活性剂TABS、催化剂SB和表面活性剂A的方法，提高产品纯度和降低游离酸的含量，成品的炭化温度为295℃，纯度大于95％。     

Identification of hairpencil secretion from maleMamestra brassicae (L.) (Lepidoptera: Noctuidae) and electroantennogram studies

Extracts of maleMamestra brassicae (L.) hairpencils were analyzed by capillary gas chromatography (GC) and by GC-mass spectrometry (GC-MS). The extracts were found to consist of six components. Benzaldehyde, 2-methylpropanoic acid, 2-methylbutanoic acid, and phenol were present in the extracts as well as the previously identified benzyl alcohol and phenyl ethanol. The two major components were 2-phenylethanol and 2-methylbutanoic acid. They represented, respectively, 74% and 12.5% of the total blend in 3-day-old male extracts. Electroantennograms were recorded on male and female antennae in response to stimulation by hairpencil compounds. Male and female antennae responded to each chemical but the female responses were significantly higher than those of the males.     

邻苯二甲酸丁苄酯的合成

叙述了邻苯二甲酸丁苄酯的市场应用概况．并介绍了二步合成法及一步合成法的实验操作．     

4,4’-二氨基二苯砜固化环氧树脂/蒙脱土纳米复合材料反应动力学的研究

选择4,4’-二氨基二苯砜（DDS）作为固化剂,采用非等温DSC法研究了双酚A缩水甘油醚型环氧树脂（E-51）/有机蒙脱土（MMT）纳米复合材料的固化反应动力学,根据Kissinger方程计算出该反应的表观活化能（ΔE）为59.91 kJ/mol,基于Crane方程计算得到该反应的反应级数为0.89,表明该反应为一复杂反应,根据固化反应动力学测试结果确定了E-51/DDS/MMT体系固化成型工艺.     

制备条件对CuZnAlZr催化剂物理性质的影响

由CO2加H2制二甲醚是CO2实现循环利用的一个重要途径.本文研究结果表明制备高比表面积CuZnAlZr催化剂的合理条件为：使用Cu、Zn、Al、Zr的硝酸盐的质量分数为10%的试剂,老化温度为130℃,老化时间为15 h,在此条件下得到比表面积为211.4 m2/g的催化剂颗粒.SEM、FT-IR、XRD表征表明催化剂颗粒为氧化物颗粒,颗粒细小,分布均匀,纯度高,为纳米颗粒.     

Hydrogen production from partial oxidation of dimethyl ether by plasma-catalyst reforming

Hydrogen was produced from partial oxidation reforming of DME （dimethyl ether） by spark discharge plasma at atmospheric pressure. A plasma-catalyst reformer was designed. A series of experiments were carried out to investigate its performance of hydrogen-rich gas production. The effects of reaction temperature, catalyst and flow rate on gas concentrations （volume fraction）, hydrogen yield, DME conversion ratio, specific energy consumption and thermal efficiency were investigated, respectively. The experimental results show that hydrogen concentration and the flow rate of produced H2 are improved when temperature increases from 300 ℃ to 700 ℃. Hydrogen yield, hydrogen concentration and the flow rate of produced H2 are substantially improved in the use of Fe-based catalyst at high temperature. Moreover, hydrogen yield and thermal efficiency are improved and change slightly when flow rate increases. When catalyst is 12 g, and flow rate increases from 35 mL/min to 210 mL/min, hydrogen yield decreases from 66.4% to 57.7%, and thermal efficiency decreases from 35.6% to 30.9%. It is anticipated that the results would serve as a good guideline to the application of hydrogen generation from hydrocarbon fuels by plasma reforming onboard.     

在运动参考系内如何正确测量时间膨胀

讨论并论证了如何正确测量时间膨胀的方法,指出了在相对于新以太运动的参考系内人们只能正确测量往返运动钟发生的时间膨胀,但却不能正确测量单向运动钟发生的时间膨胀,并以此解释了狭义相对论难以解释的一些现象,消除了人们在分析实验时所出现的多重标准.     

合成气制二甲醚三相淤浆床反应器气含率

引　言二甲醚是近年来国内外竞相开发、性能优越的碳一化工产品 .二甲醚不仅是从合成气制汽油、低碳烯烃的重要中间体 ,而且也是多种化工产品的重要原料 .同时由于二甲醚具有优良的燃烧性能和高的辛烷值 ,作为柴油的替代品日益引起人们的普遍关注 .随着对环境和生态平衡保护力度的加大 ,二甲醚的作用和地位将越来越重要 .与传统的采用固定床反应器以甲醇为原料脱水生成二甲醚的生产工艺相比 ,以煤或天然气为原料 ,通过合成气在三相淤浆床反应器中一步法合成二甲醚新工艺具有巨大的优越性 .三相淤浆床反应器流体力学性质十分复杂 ,目前还不能…     

一缩二乙醇二缩水甘油醚双丙烯酸酯的合成

以一缩二乙二醇二缩水甘油醚(DGDE)和丙烯酸为原料,N,N-二甲基苄胺为催化剂,对羟基苯甲醚为阻聚剂,制得了一缩二乙二醇二缩水甘油醚双丙烯酸酯(ADGDE)。讨论了催化剂用量、反应温度等因素对反应的影响,并用FT-IR和Photo-DSC对ADGDE的化学结构及光固化行为进行了表征。结果表明,反应温度为100℃、催化剂用量为1 0%时催化效果和反应速率较理想,用对羟基苯甲醚作阻聚剂得到的ADGDE颜色较浅;ADGDE的光聚合速率随光引发剂的用量增加而提高。     

Electro-oxidation of dimethyl ether on Pt/C and PtMe/C catalysts in sulfuric acid

The electro-oxidation of dimethyl ether (DME) on PtMe/Cs (Me = Ru, Sn, Mo, Cr, Ni, Co, and W) and Pt/C electro-catalysts were investigated in an aqueous half-cell, and compared to the methanol oxidation. The addition of a second metal enhanced the tolerance of Pt to the poisonous species during the DME oxidation reaction (DOR). The PtRu/C electro-catalyst showed the best electro-catalytic activity and the highest tolerance to the poisonous species in the low over-potential range (<0.55 V, 50 °C) among the binary electro-catalysts and the Pt/C, but at the higher potential (>ca. 0.55 V, 50 °C), the Pt/C behaved better than PtRu/C. The apparent activation energy for the DOR decreased in the order: PtRu/C (57 kJ mol⁻¹) > Pt₃Sn/C (48 kJ mol⁻¹) ≈ Pt/C (46 kJ mol⁻¹). On the other hand, the activation energy for the MOR showed a different turn, decreased in the following order: Pt/C (43 kJ mol⁻¹) > Pt₃Sn/C (35 kJ mol⁻¹) ≈ PtRu/C (34 kJ mol⁻¹). The temperature dependence of the DOR was greater than that of the oxidation of methanol (MOR) on the PtRu/C.