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51.
A fixed-bed coal gasification reactor was set up which specifically simulated the devolatilization zone in a gasifier. Samples (100 g) of lignite coal in three size ranges; ?2+1 mm, ?3+2 mm and ?4+3 mm, were devolatilized in the temperature range 350–550 °C with a steam-oxygen mixture, at 1 atm. The effect of these operating variables on tar yield and composition, melting point, viscosity, specific gravity, and molecular weight distribution was determined. A first-order reaction model was fitted to the experimentally observed total loss in weight of the lignite. 相似文献
52.
The kinetics of the hydrogen sulfide oxidation process, producing mostly sulfur and water, was studied using 0.25 to 1.0 g Hydrodarco activated carbon catalyst and varying the O2/H2S ratio (molar basis) in the feed gas between 0.5 to 0.6 in the temperature, and pressure ranges from 125 to 200°C and 225 to 780 kPa. SO2 was obtained as an undesirable by-product during H2S oxidation reaction or as a product during regeneration of the catalyst. The feed gas contained 0.9 — 1.3 mol% H2S with approximately 80 mol% CH4. In this paper, the factors affecting the H2S conversion and SO2 formation are presented. The rate expressions for (a) H2S conversion and (b) SO2 formation were developed from the Langmuir-Hinshelwood surface control reaction model. The experimental data were well correlated by the rate equations. Also, the rate parameters were evaluated and correlated with temperature. The activation energies for H2S oxidation and SO2 production reactions were calculated to be 34.2 and 62.5 kJ/mol, respectively. Partial pressures of oxygen and H2S were found to influence H2S conversion whereas, the presence of water in the feed gas up to 10.5 mol% did not affect H2S conversion significantly. Heats of adsorption for various species on the active sites were calculated. SO2 production was, as expected, enhanced at higher temperature, and its rate was much smaller than the oxidation rate of H2S under the reaction conditions used. 相似文献
53.
中氮改小氮是当前的热点,改造后的实际效果却从未见到过有说服力的报道。本文对我公司造气系统中氮改小氮流程的实践进行了定性和定量评价,意为未改者提供改造依据,为已改者提供进一步完善的思路。 相似文献
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M. A. Ali 《Petroleum Science and Technology》2013,31(10):1333-1345
Abstract A comparison of the results using Ni-W and Ni-Mo loaded catalysts with desulfurized vacuum gas oil shows that both the fixed-bed reaction and swing-batch reaction systems can be used efficiently for the catalysts evaluation. The results from a fixed-bed reaction showed that Cat-2 catalyst was more active than both Cat-1 and Cat-3, while the hydrodesulfurization (HDS) activity of Cat-3 catalyst was slightly better than that of Cat-1 and Cat-2. In the swing-batch reaction, Cat-1 and Cat-2 showed higher activity as compared to Cat-3 and Cat-4 catalysts. NiW loaded catalysts were found more active than NiMo loaded catalysts. HDS and cracking activities in the swing-batch reactor were found lower as compared to the fixed-bed reactor, probably due to recombination reactions involving sulfur and other cracked molecules. 相似文献
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采用浸渍法制备了一系列H-ZSM-5分子筛负载过渡金属锌催化剂,在固定床反应器上考察了这些催化剂对丙烯醇催化氨化合成3-甲基吡啶的催化性能。通过对H-ZSM-5的硅铝比、锌负载量对催化剂催化性能影响的考察,发现硅铝比为80、锌负载量为12%时得到的催化剂Zn12/H-ZSM-5(80)的催化性能最佳。在常压、反应温度420℃、氨醇摩尔比3:1、空速300 h-1条件下,丙烯醇在该催化剂上的转化率和3-甲基吡啶的选择性分别达到97.8%和37.9%。利用X射线衍射(XRD)、X射线光电子能谱(XPS)以及吡啶吸附红外对催化剂进行了表征,结果表明,Zn12/H-ZSM-5(80)上负载的Zn2+为L酸;在丙烯醇生成3-甲基吡啶的反应过程中催化剂的脱氢活性物种为氧化锌,而加成和环合反应则主要是由催化剂中的L酸催化实现的。 相似文献
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对城市污水污泥(简称污泥)进行工业分析和热重分析,考察污泥的基本组成和热重特性;采用气相色谱(GC)检测了不同热解温度区间内污泥热解生成的气体产物成分,并利用SEM和BET分别分析了不同热解终温下裂解炭的形貌特征和比表面积。结果表明:污泥热解可以分为水分析出阶段、挥发分析出阶段和焦炭化阶段;不同热解温度区间内污泥热解气体产物的组成有很大差别,热解温度350℃后H2在热解气中的含量快速增加,CH4含量在350~450℃时达到最大值,而CO主要在热解温度为350~750℃时生成,CO2含量随着热解温度的增加迅速下降;随着热解终温的不断升高,裂解炭结构变得越来越疏松,比表面积也随之增大,750℃达到最大值55 m2·g-1。 相似文献
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