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1.
改性纳米TiO2光催化降解苯酚活性的研究 总被引:4,自引:0,他引:4
在装有紫外光的光催化反应器中,用锐钛型纳米TiO2为光催化剂,进行了苯酚水溶液的光催化降解性能的研究。考察了溶液的pH值、纳米TiO2用量、镍(Ni^2+)掺杂量、苯酚的初始质量浓度等因素对苯酚水溶液光催化降解过程的影响。结果表明,在pH值为7时,苯酚水溶液的降解率达95%以上,强酸和强碱条件均不利于苯酚的降解。当TiO2用量为50mg,UV辐照40min时,200mL质量浓度为50mg/L的苯酚水溶液的降解率为96.3%;当TiO2用量为150mg,UV辐照60min时,200mL质量浓度100mg/L的苯酚水溶液的降解率为95.8%。镍掺杂增加了TiO2的光催化活性,用质量分数为10%的二氯化镍水溶液掺杂制备的复合光催化剂,苯酚水溶液的降解率比未掺杂时增加13.6%。 相似文献
2.
采用浸渍法制备了RuO2/γ-A12O3和RuO2/CeO2/γ-A12O3催化剂,并利用XRD、SEM和XPS对催化剂进行了表征,研究了Ce的加入对RuO2/γ-A12O3催化剂表面分散性和催化剂表面元素Ru,O和Ce化学态的影响,同时考察了RuO2/γ-A12O3和RuO2/CeO2/γ-A12O3催化剂湿式氧化降解苯酚的活性,并深入探讨了Ce对RuO2/γ-A12O3催化剂的助催化作用。结果表明:Ce掺杂改性后,使催化剂表面Ru的化学态降低、表面氧空位增加,并且活性组分Ru的分散性增加,从而使RuO2/CeO2/γ-A12O3催化剂的活性提高,因此Ce起到了显著的助催化作用。 相似文献
3.
采用溶胶-凝胶法制备了Yb掺杂TiO2纳米光催化剂,并通过XRD和BET等手段进行了表征.以对苯二甲酸作为探针分子,结合化学荧光技术研究了光催化剂表面羟基自由基的生成;并以苯酚为光催化降解反应模型化合物,考察了光催化剂的活性.测定了苯酚在TiO2和Yb掺杂TiO2光催化剂上的吸附常数.结果表明:Yb掺杂使TiO2的粒径减小,比表面积增大,同时导致羟基自由基的生成速率增大.Yb掺杂有利于反应底物在催化剂表面的吸附,Yb的最佳掺入量为Yb/Ti摩尔比=0.8%. 相似文献
4.
Wei Feng Jianping Wen Xiaoqiang Jia Qing Yuan Yan Sun Cuiyun Liu 《American Institute of Chemical Engineers》2006,52(8):2864-2875
A coupled three-dimensional (3-D) model, combining hydrodynamics with biochemical reactions, was developed to simulate the local transient flow patterns and the dynamic behaviors of cell growth and phenol biodegradation by yeast Candida tropicalis in the bubble-column bioreactor, using the computational fluid dynamic (CFD) method. In order to validate this proposed model effectively, the validation of the local hydrodynamic characteristics of the gas-mineral salt solution (gas-liquid) two-phase system, with the phenol concentration of 1200 mg/L, and with the absence of cells, was performed in a square-sectioned bubble column bioreactor using the LDA system and conductivity probe. Furthermore, the validation of phenol biodegradation behaviors by yeast Candida tropicalis at different initial concentrations of phenol and cell was also carried out in the above bubble-column bioreactor. The results indicated that the model simulations had a satisfying agreement with the experimental data. Finally, the local instantaneous flow and phenol biodegradation features including gas holdup, gas velocity, liquid velocity, cell concentration and phenol concentration inside the bioreactor were successfully predicted in different-scale bubble columns by the proposed model. © 2006 American Institute of Chemical Engineers AIChE J, 2006 相似文献
5.
Fernando J Beltrn F Javier Rivas Olga Gimeno 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2005,80(9):973-984
Photocatalytic ozonation (1O3 + VUV + TiO2), ozonation (O3), catalytic ozonation (O3 + TiO2), ozone photolysis (O3 + VUV), photocatalysis (TiO2 + VUV) and photolysis (VUV) have been compared in terms of formation of intermediates, extent of, mineralization (TOC, COD, chloride, nitrate) and kinetics in the aqueous treatment of three phenols (phenol, p‐chlorophenol and p‐nitrophenol). In all cases, photocatalytic ozonation led to lower degradation times for chemical oxygen demand and total organic carbon removal. Intermediates formed were similar in the different oxidation systems with some exceptions. They can be classified into three different types: polyphenols (resorcinol, catechol, hydroquinone), unsaturated carboxylic acids (maleic and fumaric acids) and saturated carboxylic acids (glyoxylic, formic and oxalic acids). First order kinetic equations have been checked for the oxidation processes studied in the case of the parent compound. Rate constants of these systems have also been calculated. Copyright © 2005 Society of Chemical Industry 相似文献
6.
The effect on the interfacial tension of the water toluene system has been studied at 25 °C in the presence of four phase-transfer catalysts i.e. tricaprylmethyl ammonium chloride, hexadecyltrimethyl ammonium chloride, hex-adecytrimethyl ammonium bromide and hexadecyltributyl phosphonium bromide. The interfacial tension of aqueous phenol/resorcinol-toluene in the presence and absence of tricaprylmethyl ammonium chloride has also been reported. Attempt has been made to elucidate the change in volumetric rate of extraction with different catalysts for two phase reactions, on the basis of interfacial tension. 相似文献
7.
混合型表面活性剂液膜法处理含酚废水研究 总被引:25,自引:1,他引:24
研究了兰-113B=Span-80--煤油NaOH液膜体系处理苯酚废水的最佳操作工用于对高浓度含酚废水进行处理,实验结果表明,混合型表面活性剂各项指标均较好,除酚效率可达99%以上,对内相NaOH的最佳浓度的确定给出了估算方法。 相似文献
8.
9.
New measurements of the vapor-phase viscosity of phenol were performed from 437 up to 624 K and for densities between 0.006 and 0.023 mol · L–1 in an all-quartz oscillating-disk viscometer with small gaps. Thus, including our own measurements reported earlier, experimental data are available in the temperature range between 376 and 639 K and in the density range from 0.001 up to 0.023 mol · L–1. The data were evaluated with a density series for the viscosity in which only a linear density contribution is included. The values of the second viscosity virial coefficient obtained for phenol as well as for benzene, toluene, and p-xylene were compared with results of the Rainwater-Friend theory and of the modified Enskog theory on the basis of the Lennard-Jones 12-6 potential. The agreement is reasonable, when the potential parameter ratios determined by Bich and Vogel are used. The influence of bound dimers seems to be already taken into account in the three-monomer contribution according to Hoffman and Curtiss.Paper dedicated to Professor Joseph Kestin. 相似文献
10.
合成2,4-二叔丁基苯酚工业试验 总被引:2,自引:0,他引:2
以离子交换树脂为催化剂,苯酚和甲基叔丁基醚为原料合成2,4-二叔丁基苯酚(简称2,4酚),合成产物经过滤再经间歇真空精馏精制提纯,得到高纯度的2,4酚成品。成品精馏后釜中残液在酸性白土催化剂的作用下通过歧化反应生成对叔丁基苯酚,再经精馏提纯得到成品对叔丁基苯酚。通过工艺优化,使2,4酚、对叔丁基苯酚形成联产生产工艺,降低了生产原料消耗和成本。 相似文献