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1.
本文阐述了通过Friedel-Crafts反应合成邻-(4-乙基苯甲酰基)苯甲酸的方法.研究了影响产物质量的因素,提出了适宜的工艺条件. 相似文献
2.
Biodegradation of monoaromatic hydrocarbons in aquifer columns amended with hydrogen peroxide and nitrate 总被引:1,自引:0,他引:1
The ability of indigenous microorganisms to degrade benzene, toluene, ethylbenzene and xylenes (BTEX) in laboratory scale flow-through aquifer columns was tested separately with hydrogen peroxide (110 mg/l) and nitrate (330 mg/l as NO3−) amendments to air-saturated influent nutrient solution. The continuous removal of individual components from all columns relative to the sterile controls provided evidence for biodegradation. In the presence of hydrogen peroxide, the indigeneous microorganisms degraded benzene and toluene (> 95%), meta- plus para-xylene (80%) and ortho-xylene (70%). Nitrate addition resulted in 90% removal of toluene and 25% removal of ortho-xylene. However, benzene, ethylbenzene, meta- and para-xylene concentrations were not significantly reduced after 42 days of operation. Following this experiment, low dissolved oxygen (< 1 mg/l) conditions were initiated with the nitrate-amended column influent in order to mimic contaminated groundwater conditions distal from a nutrient injection well. Toluene continued to be effectively degraded (> 90%), and more than 25% of the benzene, 40% of the ethylbenzene, 50% of the meta- plus para-xylenes and 60% of the ortho-xylene were removed after several months of operation. 相似文献
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在上海石油化工研究院开发的分子筛催化剂和联合化学反应工程研究所华东化工学院分所小试过程开发的基础上,建立了年产300t乙苯的中试装置,进行了由乙烯、苯气相烷基化合成乙苯的中试研究,为工业生产提供了设计依据。 相似文献
5.
论述了用于C8芳烃中二甲苯异构体以及乙苯分离的各种吸附分离技术进展,对各种工艺和特点以及工业应用状况进行了分析比较。详细介绍了目前国内C8芳烃吸附分离装置中的工业生产状况和面临的问题及挑战。提出应抓紧开发具有自主知识产权的C8芳烃吸附分离技术,尤其是开发一种对乙苯和二甲苯同时具有高选择性、高吸附能力、容易脱附的吸附剂,实现从C8芳烃中同时得到乙苯和二甲苯高纯度产品的目的,打破国外的技术垄断。 相似文献
6.
以脱硫后的正庚烷为溶剂,采用微库仑法测定乙苯中微量硫的最佳条件为:氩气/氧气为160/40(体积比),进样速度5μL/min,预热温度420℃,燃烧温度760℃,出口区温度640℃,电解液用二次脱盐水配制。微库仑法的准确度和精密度均高于国际标准(ISO)的氢氧焰法。 相似文献
7.
The chemical equilibrium for the coupling of ethylbenzene dehydrogenation with nitrobenzene hydrogenation, to produce styrene and aniline simultaneously, has been calculated on the basis of the Soave–Redlich–Kwong equation of state. The dehydrogenation of ethylbenzene in the presence of nitrobenzene over the catalysts -Al2O3, ZSM-5, activated carbon and platinum supported on activated carbon has been carried out at 400 °C. The effects of Pt loading and the pretreatment of the catalysts have been investigated. It has been revealed that the conversion of ethylbenzene can be greatly improved by the reaction coupling due to the elimination of the hydrogen produced in the reaction by the hydrogenation of nitrobenzene. Platinum supported on the activated carbon has been suggested as a suitable catalyst. The best results with ethylbenzene conversion of 33.8% and styrene selectivity of 99.2% were obtained over Pt(0.02 wt%)/AC at 400 °C. Moreover, such process is also energetically favored since the necessary process heat to drive the ethylbenzene dehydrogenation can be provided by the coupling with the exothermic nitrobenzene hydrogenation reaction. 相似文献
8.
Alumina supported vanadia catalysts (V/Al) for selective oxidehydrogenation of ethylbenzene with CO2 were prepared by impregnation method. During preparation the effect of promoters and calcined temperature was investigated,
it was found these two items had a strong influence on the activity of V/Al catalysts. Dehydrogenation reaction with CO2 was happened in the fixed-bed reactor at 450 °C. Results showed that 15.2% ethylbenzene conversion and 99.2% styrene selectivity
were acquired when V2K/Al catalyst was used. 相似文献
9.
Hong Ma Jie Xu Chen Chen Qiaohong Zhang Jianbo Ning Hong Miao Lipeng Zhou Xiaoqiang Li 《Catalysis Letters》2007,113(3-4):104-108
Co(II)O was highly dispersed in the mesopores of SBA-15 by alcoholic impregnation method and characterized by XRD, TEM, UV–VIS
DRS, TPR, and XRF techniques. It was found that tetrahedral coordinated Co(II)O was stabilized by SBA-15 at low Co-loading.
Co/SBA-15 showed much higher activity than Co(OAc)2 or Co3O4 in the liquid-phase aerobic oxidation of ethylbenzene under solvent-free condition. 相似文献
10.