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71.
采用还原性有机酸络合铁离子并负载到活性炭纤维(ACFs)上,制备出非均相Fenton催化剂用于去除染料废水中有机污染物.采用SEM、FTIR和ICP-AES对制备出的草酸铁(Oxa-Fe)络合物负载ACFs(Oxa-Fe/ACFs-3)进行了表征.发现草酸铁络合物均匀负载在ACFs上,其中铁的质量分数为0.96%.在Oxa-Fe/ACFs-3和H2O2添加量分别为10 g/L和100 mmol/L(以染料废水体积计),50℃条件下对20 mL染料废水进行了降解,染料废水化学需氧量(COD)去除率在100 min内可达62.2%.此外,考察了该催化剂pH适用范围以及重复使用性能.结果表明,Oxa-Fe/ACFs-3促进了H2O2活化产生活性自由基?OH和?O2–,实现了对染料废水中有机污染物的降解.对比了不同还原性有机酸络合铁负载ACFs处理染料废水的性能,发现有机酸还原性越强,越有利于染料废水COD去除率的提高.  相似文献   
72.
Three MgO surfaces of different structures have been employed as models for study of the acid-base properties of MgO. Surface spectroscopies including XPS, UPS, and ISS were used to determine the nature and the absolute coverage of surface intermediates, and the nature of bonding sites upon adsorption of Brønsted acid molecules on these surfaces. Different behavior patterns of the Brønsted acid molecules with varying strengths on the three model surfaces provide insights into the site requirements for dissociation of Brønsted acids on MgO. The base-catalyzed Cannizzaro reaction of formaldehyde was observed on these model surfaces under UHV conditions.  相似文献   
73.
The effects of oxyen plasma treatment on the surface chemistry of Spectra 1000® high modulus polyethylene fibers and on the mechanical properties of fiber-reinforced composites of the fibers in a Bis-GMA based acrylic resin have been studied. X-ray photoelectron spectroscopy and diffuse reflectance FTIR spectroscopy have been used to show that the majority of oxygen on the fiber surface exists mostly in the form of ether and/or epoxy linkages, with carbonyl-, carboxylic- and ester-containing compounds accounting for less than 10 percent of the total. While the untreated and plasma-treated fibers have similar chemical compositions, the surfaces of the plasma-treated fibers are more polar and the oxygen is chemically bonded instead of being merely physisorbed. The interfacial shear strength between the fibers and the acrylic resin is increased by a factor of 2.3 by the plasma treatment indicating the presence of a weak boundary layer on the surface of the untreated fibers. The hydrolytic stability of the composite interfaces was investigated for fibers sized with several Bis-GMA-based adhesives. Maximum stability was attained by sizing with Bis-GMA containing a peroxide catalyst or an amine accelerator. The flexural properties of composites utilizing plasma-treated and untreated fibers were compared in three-point bending. The ultimate bending loads for composites using treated fibers were much higher than those for composites with untreated fibers, but only a fraction of that for glass or Kevlar®-reinforced materials.  相似文献   
74.
成绍鑫 《腐植酸》2007,(1):1-11
我国土壤污染形势严峻,已成为农产品安全和农业可持续发展的一大障碍."十一五"期间已将防治土壤污染列入重要议事日程,"全国土壤污染状况调查和防治项目"业已启动,2006年11月<农产品质量安全法>也开始实施.腐植酸学术界及行业又面临新的机遇和挑战.介绍了我国土壤污染的现状及其治理技术,阐述了腐植酸类物质(HS)修复污染土壤的研究进展、存在问题及应用的可行性,并对今后的研究开发及应用方向提出若干建议.  相似文献   
75.
Leaf quality of the mountain birch (Betula pubescens ssp.tortuosa) for herbivores was studied at several hierarchical levels: among trees, among ramets within trees, among branches within ramets, and among short shoots within branches. The experimental units at each level were chosen randomly. The indices of leaf quality were the growth rate of the larvae of a geometrid,Epirrita autumnata, and certain biochemical traits of the leaves (total phenolics and individual phenolic compounds, total carbohydrates and individual sugars, free and protein-bound amino acids). We also discuss relationships between larval growth rate and biochemical foliage traits. Larval growth rates during two successive years correlated positively at the level of tree, the ramet, and the branch, indicating that the relationships in leaf quality remained constant between seasons both among and within trees. The distribution of variation at different hierarchical levels depended on the trait in question. In the case of larval growth rate, ramets and short shoots accounted for most of the explained variation. In the case of biochemical compounds, trees accounted for most of the variance in the content of total phenolics and individual low-molecular-weight phenolics. In the content of carbohydrates (total carbohydrates, starch, fructose, glucose, and sucrose) and amino acids, variation among branches was generally larger than variation among trees. Variation among ramets was low for most compounds. No single leaf trait played a paramount role in larval growth. Secondary compounds, represented by phenolic compounds, or primary metabolites, particularly sugars, may both be important in determining the suitability of birch leaves for larvae. If phenols are causally more important, genet-specific analyses of foliage chemistry are needed. If sugars are of primary importance, within-genet sampling and analysis of foliage chemistry are necessary.  相似文献   
76.
对前文 (I)的共聚动力学模型进行了分析与简化 ,并分别通过对各影响因素的单因素实验和多因素相互作用实验对模型进行了进一步的考核 ,确定了模型参数并通过模型对聚合动力学行为作了说明  相似文献   
77.
NIR spectroscopy calibrations have been developed for a range of quality parameters in olive oil, including FFA, PV, polyphenol content, induction time, chlorophyll, and the major FA. A set of 216 olive oil samples from throughout the Australian olive-growing areas were used to provide a representative range of quality. The variation in the oils tested virtually covered the range of the chemical standard limits described by the International Olive Oil Council. A FOSS NIRSystems® 6500 spectrophotometer with a liquid cell holder was used. Multiple correlation coefficients squared (R 2) for minor components stearic acid (0.86), and linolenic acid (0.85) were relatively low because the concentration range is very narrow compared with the reproducibility of the reference method. However, the major FA, oleic (0.99) and linoleic (1.00), FFA (0.97), and chlorophyll (0.98) provided high levels of accuracy. All of the parameters measured were sufficiently accurate for routine screening of olive oil.  相似文献   
78.
本文介绍了以3-硝基-2-叔丁氧甲酰氨基苯甲酸乙酯为原料,在碱性条件下与4-(2-氰基苯基)-1-溴甲苯发生亲核取代反应制备2-[(2′-氰基联苯-4-基)甲基氨基]-3-硝苯甲酸乙酯的方法,产品经核磁共振验证其结构,产品收率达83%。本合成工艺条件温和,适合工业化生产。  相似文献   
79.
以氰化钠、碳酸铵、乙醛等为原料,常压下一步反应得到5甲基海因,总收率702%。其最佳操作条件为:反应温度75℃,反应时间3h,原料碳酸铵与氰化钠之比为2∶1,酸化回流pH值为2,酸化回流时间2h。  相似文献   
80.
中试规模制备L-茶氨酸及其衍生物   总被引:6,自引:0,他引:6  
报道了中试规模制备L-茶氨酸和L-谷氨酰胺的一种方法。以廉价的L-谷氨酸为原料,采用邻苯二甲酰基作为保护基,保护L-谷氨酸的α-氨基,醋酐回流10 m in使其分子内脱水生成N-邻苯二甲酰-L-谷氨酸酐,在常温、常压条件下,分别与2 mol/L氨水和2 mol/L乙胺水溶液反应生成中间产物N-邻苯二甲酰-L-谷氨酰胺、N-邻苯二甲酰-L-茶氨酸,中间产物在室温条件下与0.5 mol/L水合肼反应48 h脱除保护基,分别以57%、61%的收率得到L-谷氨酰胺和L-茶氨酸。  相似文献   
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