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排序方式: 共有1195条查询结果,搜索用时 15 毫秒
1.
Yu Zhao Zhigang Xu Zongshi Li Weihong Qiao Lubai Cheng 《Petroleum Science and Technology》2006,24(7):821-827
Heavy alkyl benzene sulfonates (HABS) were synthesized, and their interfacial tensions were measured and compared with those of petroleum sulfonates ORS-41. Effects of their coupling with lignosulfonate were also studied. The results showed that HABS exhibited good interfacial activities and the system of HABS blending with LS displayed better interfacial activities than ORS-41 and therefore reduced the prime cost. Their best proportions of synergism were from 3:1 to 4:1. HABS might be a more promising alkali-surfactant-polymer (ASP) flooding agent. 相似文献
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相转移催化合成芳基烷基醚 总被引:7,自引:0,他引:7
报道了以四丁基溴化铵为相转移催化剂,简便地合成了10个芳基烷基醚,反应几乎是定量地快速进行。 相似文献
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丙烯酸高碳醇酯的合成 总被引:1,自引:0,他引:1
介绍了降凝剂中间体丙烯酸高碳醇酯的合成和产品分离提纯方法。考察了合成条件对酯化反应的影响,结果表明,在原料丙烯酸与十八醇摩尔比1.2:1,阻聚剂对苯二酚用量占原料总量1.5%,催化剂对甲苯磺酸用量占原料总量1.5%,反应温度80-86℃,回流反应时间6h条件下,酯化率最高达89%。产品分离提纯方法与传统分离方法比较,所需分离时间短,洗涤用水量少,而产品收率远高于传统分离方法,达95%以上。 相似文献
7.
B.S. Kirkland 《Polymer》2008,49(2):507-524
Poly(n-alkyl acrylate)s can have side chains that crystallize independently of the main chain; side-chain length can thus be used as a tunable parameter to control the gas permeability of membranes. The gas permeation response of poly(n-alkyl acrylate) and poly(m-alkyl acrylate) blends as a function of temperature is reported for varying side-chain lengths, n and m, and blend composition in the semi-crystalline and molten states. Macroscopic homogeneity is observed for a small range of n and m where |n − m| ≤ 2-4 methylene units. Thermal analysis indicates that the blend components crystallize independently of one another; however, crystallization is hindered by the presence of the other component. Permeation responses of the blends investigated in some cases exhibited two distinct permeation jumps or increases at the melting temperature of each component. Blends with continuous permeation responses but higher effective activation energies of permeation (i.e., more thermally responsive) were observed for some blends over the temperature of interest for membranes to be used for modified atmosphere packaging. 相似文献
8.
Per Munk Nielsen Jesper Brask Lene Fjerbaek 《European Journal of Lipid Science and Technology》2008,110(8):692-700
It is well documented in the literature that enzymatic processing of oils and fats for biodiesel is technically feasible. However, with very few exceptions, enzyme technology is not currently used in commercial‐scale biodiesel production. This is mainly due to non‐optimized process design and a lack of available cost‐effective enzymes. The technology to re‐use enzymes has typically proven insufficient for the processes to be competitive. However, literature data documenting the productivity of enzymatic biodiesel together with the development of new immobilization technology indicates that enzyme catalysts can become cost effective compared to chemical processing. This work reviews the enzymatic processing of oils and fats into biodiesel with focus on process design and economy. 相似文献
9.
OPS和OPC系列稠油乳化降黏剂的研制 总被引:1,自引:0,他引:1
以工业品烷基酚聚氧乙烯醚OP-n(n=4,6,8,10,15)为起始原料,合成了烷基酚聚氧乙烯醚乙酸盐OPC-n和磺酸盐OPS-n两个系列的阴-非离子表面活性剂。以酸值和黏度不同的胜利单家寺和陈庄稠油为实验油样。将OPC-n和OPS-n溶于矿化度5811 mg/kg的胜利标准盐水和NaCl、CaCl2盐水中作为水相,按油、水质量比7∶3在50℃用玻棒搅拌混合,观察是否形成水包油乳状液并测黏度进行确认。在胜利标准盐水溶液中,OPC-n和OPS-n乳化稠油所需的最低质量分数,随稠油、表面活性剂类型及氧乙烯链节数n而变,一般而言,OPC-n系列中的OPC-8和OPS-n系列中的OPS-4乳化稠油的性能最好,该最低质量分数值分别为0.05%或0.025%和0.025%。在NaCl盐水溶液中,OPC-n的该最低质量分数值与稠油和n有关,均随盐含量增加而增大,在盐含量≤15%时,抗盐性最好的OPC-8和OPC-10的该值≤0.05%;OPS-n的抗盐性好于OPC-n。OPC-n的抗钙性良好,钙盐含量为2%时该最低质量分数≤0.1%;OPS-n的抗钙性更好,钙盐含量为2%和3%时该最低质量分数仅为0.025%或0.05%。表6参5。 相似文献
10.
Dr. Qingyun Tang Assist. Prof. Dr. Ioannis V. Pavlidis Dr. Christoffel P. S. Badenhorst Prof. Dr. Uwe T. Bornscheuer 《Chembiochem : a European journal of chemical biology》2021,22(16):2584-2590
Halide methyltransferases (HMTs) enable the enzymatic synthesis of S-adenosyl-l -methionine (SAM) from S-adenosyl-l -homocysteine (SAH) and methyl iodide. Characterisation of a range of naturally occurring HMTs and subsequent protein engineering led to HMT variants capable of synthesising ethyl, propyl, and allyl analogues of SAM. Notably, HMTs do not depend on chemical synthesis of methionine analogues, as required by methionine adenosyltransferases (MATs). However, at the moment MATs have a much broader substrate scope than the HMTs. Herein we provide an overview of the discovery and engineering of promiscuous HMTs and how these strategies will pave the way towards a toolbox of HMT variants for versatile chemo- and regioselective biocatalytic alkylations. 相似文献