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51.
Young Sil Jeon Jing Lei Ji-Heung Kim 《Journal of Industrial and Engineering Chemistry》2008,14(6):726-731
This study examined the removal of some basic dyes, such as Methylene Blue, Malachite Green and Methyl Orange, using alginate or alginate/polyaspartate composite gel beads. The adsorption of dyes from aqueous solutions at 25 °C was examined using a batch sorption technique. The effects of CaCl2 and the dye concentration on the adsorption were examined. Type-S adsorption isotherms were obtained, which is characteristic of a weak solute–solid interaction. The ionic interaction between the dye molecule and gel matrix appears to be responsible for the efficient adsorption of cationic dyes in this system. These results suggest that an alginate/polyaspartate gel can be used as an effective sorbent for water pollutants such as dyes, and the immobilization of these organic contaminants in the hydrogels from wastewater can solve one of the most important environmental problems in the related industry. 相似文献
52.
A self-assembled monolayer (SAM) of p-hydroxymethylbenzene HOCH2C6H4 - (HOMB) moiety adsorbed on iron by the formation of a covalent bond between carbon and iron atoms was prepared by electrochemical derivatization of an iron electrode with p-hydroxymethylbenzenediazonium tetrafluoroborate HOCH2C6H4N2BF4. The electrode covered with the HOMB SAM was modified with alkyltriethoxysilanes CnH2n+1Si(OC2H5)3 (CnTES, n = 8 or 18) to prepare a film of one-dimensional polymer. The protective ability of the polymer film was determined by polarization measurement of the covered electrode in an aerated 0.5 M NaCl solution. The ability was enhanced by modification of the HOMB SAM with CnTES markedly. The iron surface coated with the one-dimensional polymer film of the HOMB SAM modified with C8TES was characterized by contact angle measurement and FTIR reflection and X-ray photoelectron spectroscopies. The persistence in the protective ability of the polymer film against iron corrosion in 0.5 M NaCl may be associated with the strong adsorption via the covalent bond, revealed by electron-probe microanalysis. 相似文献
53.
研究了不同温度下PTT(聚对苯二甲酸丙二醇酯)直接酯化反应动力学。建立了零级和一级反应动力学模型。用实验数据进行的检验表明,一级动力学模型更为接近该反应过程。 相似文献
54.
Ring‐opening polymerization of D,L ‐lactide (LA) has been successfully carried out by using rare earth 2,6‐dimethylaryloxide (Ln(ODMP)3) as single component catalyst or initiator for the first time. The effects of different rare earth elements, solvents, monomers and catalyst concentration as well as polymerization temperature and time on the polymerization were investigated. The results show that La(ODMP)3 exhibits higher activity to prepare poly(D,L ‐lactide) (PLA) with a viscosity molecular weight of 4.5 × 104 g mol?1 and the conversion of 97 % at 100 °C in 45 min. The catalytic activity of Ln(ODMP)3 has following sequence: La > Nd > Sm > Gd > Er > Y. A kinetic study has indicated that the polymerization is first order with respect to both monomer and catalyst concentration. The apparent activation energy of the polymerization of LA with La(ODMP)3 is 69.6 kJ mol?1. The analyses of polymer ends indicate that the LA polymerization proceeds according to ‘coordination–insertion’ mechanism with selective cleavage of the acyl–oxygen bond of the monomer. Copyright © 2004 Society of Chemical Industry 相似文献
55.
56.
高温和低张应力引起的非平衡晶界偏聚动力学(Ⅱ)--实验结果的动力学模拟 总被引:2,自引:2,他引:0
以文献[1]建立的张应力引起的非平衡晶界偏聚动力学方程模拟了Shinoda T等的磷在钢中的应力时效实验结果和Misra R D K的硫在钢中的应力时效实验结果,模拟结果与实验结果互相吻合。通过模拟发现,张应力使磷-空位复合体以及硫-空位复合体在钢中的扩散系数均增加3个数量级,且磷原子和硫原子的扩散系数分别降低3个和5个数量级。 相似文献
57.
研究了在超临界条件下甘油三乙酸酯与甲醇或乙醇的酯交换反应,分别考察了超临界状态下醇油摩尔比和温度对反应的影响。实验结果表明,甲醇或乙醇与甘油三乙酸酯的摩尔比为14、反应温度为350℃、反应时间为20m in时,乙酸甲酯或乙酸乙酯的收率分别达100%和60%。对超临界状态下动力学的研究结果表明,甘油三乙酸酯与甲醇或乙醇的酯交换反应为拟一级反应,在相同的反应条件下,采用甲醇时酯交换反应速率比用乙醇时快,相应的甘油三乙酸酯的转化率也高;甘油三乙酸酯在超临界甲醇或乙醇中酯交换反应的表观活化能分别为58.7 kJ/mol和75.1 kJ/mol,甘油三乙酸酯与甲醇酯交换反应的活化能低于与乙醇酯交换反应的活化能,表明碳链短的醇更易进行酯交换反应。 相似文献
58.
59.
As a consequence of the phasing out of CFCs, sorption systems appear to be potential candidates to replace vapour compression systems. Amongst sorption systems there exists a choice between several systems, such as liquid absorption, solid adsorption and chemical reaction heat pumps. Nevertheless, few comparative studies between these systems have been undertaken so far. It is the aim of this paper to present such a study based on combined first and second law thermodynamical analysis of the different cycles. Simple entropy generation processes explain why the basic cycles for these systems yield performances much lower than the Carnot efficiency. The possibility of operating regenerative cycles with internal heat recovery and higher efficiencies has also been considered for typical common base conditions. Different entropy generation considerations have been visualised, such as thermal coupling (external/internal), non-uniform temperature component entropy production and other irreversible processes for the COP degradation in these systems. It is found that thermal coupling irreversibilities in solid sorption systems and other internal irreversibilities in liquid sorption systems with solution heat exchanger are dominant in the actual COP degradation with respect to the reversible Carnot COP. 相似文献
60.
重馏分油加氢脱氮反应动力学模型的研究 总被引:10,自引:1,他引:9
简要地介绍了一些典型的模型氮化物的HDN反应规律。根据胜利VGO在3722B催化剂上的大量HDN实验数据,提出了如下的HDN基本反应动力学方程:dCNdt=-k1+K*CNCNPH2为了扩大上式的应用范围,详细分析了各种因素(如原料油种类和馏程及H2S等)对HDN的影响,并开发了相应的经验关联式,从而得到了一个较完整的馏分油HDN反应动力学模型。验证实验表明,该模型是成功的。 相似文献