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51.
料温对RIM交联型聚氨酯脲结构与性能的影响 总被引:1,自引:0,他引:1
采用便携式微型反应注射成型机制备了一组料温分别为30,40,50,60℃的交联型聚氨酯脲。用DSC和力学性能对试样进行表征的结果表明:料温提高有利于软、硬微相的混合,而硬链段微区的有序性变差。反映在宏观力学性能上则表现为:试样的拉伸强度提高,伸长率在50℃料温时出现极大值,弯曲强度和弯曲模量则出现最小值。料温为30℃时,物料混合不充分,随着料温升高,混合逐渐均匀,试样透明度提高。 相似文献
52.
介绍中石油宁夏石化分公司二化肥尿素装置的现状,拟采用二氧化碳汽提法对装置进行50%扩能改造,分析改造方案的可行性。 相似文献
53.
Toshihiro Nagao Yuji Shimada Yoshie Yamauchi-Sato Takaya Yamamoto Masaaki Kasai Kentaro Tsutsumi Akio Sugihara Yoshio Tominaga 《Journal of the American Oil Chemists' Society》2002,79(3):303-308
A commercial product of CLA contains almost equal amounts of cis-9,trans-11 (c9,t11)-CLA and trans-10,cis-12 (t10,c12)-CLA. We attempted to enrich the two isomers by a two-step selective esterification using Candida rugosa lipase that acted on c9,t11-CLA more strongly than on t10,c12-CLA. An FFA mixture containing CLA isomers was esterified with an equimolar amount of lauryl alcohol in a mixture of 20%
water and the lipase. When the esterification of total FA reached 50%, two isomers were fractionated in a good yield: t10,c12-CLA was enriched in FFA, and c9,t11-CLA was recovered in lauryl esters. The FFA were esterified again to enrich t10,c12-CLA. At 27.3% esterification of total FA, the t10,c12-CLA content in FFA increased to 64.8 wt% with 89.3% recovery: The ratio of the content of t10,c12-CLA to that of two isomers was 95.9%. Lauryl esters obtained by the single esterification were employed for enrichment
of c9,t11-CLA. After the esters were hydrolyzed, the resulting FFA were esterified again with lauryl alcohol. At 62.0% esterification
of total FA, the c9,t11-CLA content in lauryl esters increased to 73.3 wt% with 79.4% recovery: The ratio of the content of c9,t11-CLA to that of two isomers was 95.6%. In a 600-g-scale purification, molecular distillation was effective in separating
the reaction mixture into lauryl alcohol, FFA, and lauryl ester fractions. 相似文献
54.
55.
对严重影响大颗粒尿素流化床造粒机尿液喷射系统正常运行的多项故障进行了剖析,从生产技术改造及操作管理方面提出了改进和防范措施,结果表明,改进后装置运行周期从不足10天延长到40天。 相似文献
56.
Christine Baatz Nadine Thielecke Ulf Prüße 《Applied catalysis. B, Environmental》2007,70(1-4):653-660
In this work, two deposition–precipitation methods for the preparation of gold catalysts for glucose oxidation were investigated. Thus far, gold colloids immobilized on carbon have been used for catalytic glucose oxidation, but the long-term stability of these systems was not sufficient. To improve the long-term stability we used the deposition–precipitation methods using NaOH (DP NaOH) or urea (DP urea) as precipitation agents as they were described by Haruta and Dekkers, respectively, using alumina as a support material. With these methods, it was possible to prepare highly active and selective catalysts which showed an excellent long-term stability. DP urea was found to be the preferred method, because in contrast to DP NaOH, no losses of gold occurred during the preparation, and it was possible to adjust various gold contents up to 10 wt% Au. 相似文献
57.
Philipp Hauck Andreas Jentys Johannes A. Lercher 《Applied catalysis. B, Environmental》2007,70(1-4):91-99
In order to meet the stricter NOx and particulate emission limits for commercial vehicles, the selective catalytic reduction (SCR) with urea is currently seen having the highest potential. The conversion of urea into ammonia and carbon dioxide consists of two consecutive reactions, in which isocyanic acid is an intermediate that is hydrolyzed over TiO2. The intrinsic kinetics and the surface chemistry for this reaction are explored. Up to a temperature of 132 °C the reaction was in the intrinsic kinetic regime (EA = 73 kJ/mol), while at higher temperatures the reaction was limited by pore and external diffusion constraints, respectively. In the presence of NO, NH3 and NO2, the catalytic activity was negatively influenced, increasing in severity in the sequence mentioned indicating that nitrates formed from NO2 were most effective in blocking cations and anions of TiO2. IR spectroscopy indicates that dissociative adsorption of HNCO on TiO2 forms Ti–NCO and hydrogen bonded OH species. In the presence of water, isocyanic acid was so rapidly hydrolyzed that only adsorbed ammonia was observed on the catalyst surface. The presence of NO, NH3 and NO2 retards hydrolysis leading to the appearance of isocyanate species on the surface. 相似文献
58.
介绍在团粒法工艺的基础上 ,将尿素熔融成尿液或用尿素车间二段蒸发器的尿液进行喷浆造粒生产复合肥的改造方案、改造内容、改造效果和投资情况。 相似文献
59.
A field experiment was conducted on an acid sulfate soil in Thailand to determine the effect of N fertilization practices on the fate of fertilizer-N and yield of lowland rice (Oryza sativa L.). A delayed broadcast application of ammonium phosphate sulfate (16-20-0) or urea was compared with basal incorporation of urea, deep placement of urea as urea supergranules (USG), and amendment of urea with a urease inhibitor. Deep placement of urea as USG significantly reduced floodwater urea- and ammoniacal-N concentrations following N application but did not reduce N loss, as determined from an15N balance, in this experiment where runoff loss was prevented. The urease inhibitor, phenyl phosphorodiamidate (PPD), had little effect on floodwater urea- and ammoniacal-N, and it did not reduce N loss. The floodwater pH never exceeded 4.5 in the 7 days following the first N applications, and application of 16-20-0 reduced floodwater pH by 0.1 to 0.3 units below the no-N control. The low floodwater pH indicated that ammonia volatilization was unimportant for all the N fertilization practices. Floodwater ammoniacal-N concentrations following application of urea or 16-20-0 were greater on this Sulfic Tropaquept than on an Andaqueptic Haplaquoll with near neutral pH and alkaline floodwater. The prolonged, high floodwater N concentrations on this Sulfic Tropaquept suggested that runoff loss of applied N might be a potentially serious problem when heavy rainfall or poor water control follow N fertilization. The unaccounted-for15N in the15N balances, which presumably represented gaseous N losses, ranged from 20 to 26% of the applied N and was unaffected by urea fertilization practice. Grain yield and N uptake were significantly increased with applied N, but grain yield was not significantly affected by urea fertilization practice. Yield was significantly lower (P = 0.05) for 16-20-0 than for urea; however, this difference in yield might be due to later application of P and hence delayed availability of P in the 16-20-0 treatment. 相似文献
60.
Katariina Rahkamaa-Tolonen Teuvo Maunula Mari Lomma Mika Huuhtanen Riitta L. Keiski 《Catalysis Today》2005,100(3-4):217-222
The activity of fresh and hydrothermally aged zeolite-based catalysts in the NH3-selective catalytic reduction (SCR) reaction with excess of oxygen were studied. In addition, the effect of NO2 in the gas feed as well as the acidity of the catalysts for the SCR activity was investigated. The studied catalysts were hydrogen, copper, iron and silver ion exchanged ZSM-5, mordenite, beta, ferrierite, and Y-zeolites. The investigation verifies that the zeolite-based catalysts are very promising for the ammonia SCR reaction. Especially, the activity at low and high temperatures was higher than the activity of commercial vanadia-based catalysts. From the studied catalysts, Fe-beta was the most potential one. The presence of NO2 in the inlet flow enhanced significantly the catalytic activity of fresh and hydrothermally aged zeolite catalysts. This suggests that the oxidation of NO to NO2 is probably the rate-determining step for the SCR reaction. 相似文献