全文获取类型
收费全文 | 74508篇 |
免费 | 21954篇 |
国内免费 | 1770篇 |
专业分类
电工技术 | 3071篇 |
综合类 | 1569篇 |
化学工业 | 26616篇 |
金属工艺 | 2466篇 |
机械仪表 | 2945篇 |
建筑科学 | 2656篇 |
矿业工程 | 211篇 |
能源动力 | 2411篇 |
轻工业 | 8391篇 |
水利工程 | 443篇 |
石油天然气 | 491篇 |
武器工业 | 433篇 |
无线电 | 13925篇 |
一般工业技术 | 20967篇 |
冶金工业 | 1606篇 |
原子能技术 | 440篇 |
自动化技术 | 9591篇 |
出版年
2024年 | 72篇 |
2023年 | 321篇 |
2022年 | 452篇 |
2021年 | 951篇 |
2020年 | 3363篇 |
2019年 | 5977篇 |
2018年 | 5457篇 |
2017年 | 6155篇 |
2016年 | 5946篇 |
2015年 | 5849篇 |
2014年 | 6121篇 |
2013年 | 6640篇 |
2012年 | 5761篇 |
2011年 | 5613篇 |
2010年 | 4419篇 |
2009年 | 4248篇 |
2008年 | 4050篇 |
2007年 | 4022篇 |
2006年 | 3869篇 |
2005年 | 3250篇 |
2004年 | 2836篇 |
2003年 | 2580篇 |
2002年 | 2472篇 |
2001年 | 2060篇 |
2000年 | 1828篇 |
1999年 | 1166篇 |
1998年 | 379篇 |
1997年 | 358篇 |
1996年 | 334篇 |
1995年 | 305篇 |
1994年 | 287篇 |
1993年 | 219篇 |
1992年 | 169篇 |
1991年 | 163篇 |
1990年 | 129篇 |
1989年 | 95篇 |
1988年 | 65篇 |
1987年 | 38篇 |
1986年 | 36篇 |
1985年 | 38篇 |
1984年 | 29篇 |
1983年 | 26篇 |
1982年 | 29篇 |
1980年 | 10篇 |
1979年 | 9篇 |
1977年 | 6篇 |
1976年 | 4篇 |
1975年 | 6篇 |
1974年 | 6篇 |
1959年 | 4篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
991.
Concentrated inverse emulsion polymerization was used for making chromatography columns (based on crosslinked polystyrene divinylbenzene (PS‐DVB)) with pore sizes less than 10 μm. According to DSC‐thermal gravimetry thermograms, it was confirmed that the residual monomer concentration after polymerization process is negligible. For application of these columns in chiral chromatography, the β‐cyclodextrin is chemically fixed on the PS‐DVB resin pore surface. The presence of hydroxyl groups in the PS‐DVB resin after chemical modification was confirmed by FTIR spectroscopy. By chemical modification of the PS‐DVB resin, thermal stability increased up to 446°C. The structure of columns was analyzed by scanning electron microscopy (SEM). SEM evaluations showed that the porous structure of PS‐DVB resin was maintained intact after the chemical modification with β‐cyclodextrin. According to X‐ray data, presence of the crystalline domain that is related to β‐cyclodextrin is confirmed.© 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 857–863, 2006 相似文献
992.
在同成分铌酸锂晶体中掺入0.03?2O3和0.1%MnO2(质量分数),分别掺入0,1%,3%,4.5%,6%的MgO(摩尔分数),用提拉法生长了一系列Mg:Mn:Fe:LiNbO3晶体.检测了Mg:Mn:Fe:LiNbO3晶体的红外光谱和抗光损伤能力.掺0,1%,3%,4.5%Mg的Mg:Mn:Fe:LiNbO3晶体的OH-红外振动峰位于3484cm-1,而掺6%Mg的Mg:Mn:Fe:LiNbO3晶体红外振动峰移到3 535gm-1.采用波长为632nm的He-Ne激光器作为光源,通过二波耦合方法测试晶体的全息存储性能.结果表明:Mg:Mn:Fe:LiNbO3晶体的写入时间和动态范围随掺镁量的增加而显著减小,而光折变灵敏度略有上升,抗光损伤性能增强,其中掺镁量为3%Mg:Mn:Fe:LiNbO3晶体更适合作为全息存储介质. 相似文献
993.
The thermal properties of amorphous gelatin films and gelatin films with renatured structural order were measured by using conventional and temperature modulated differential scanning calorimetry (DSC). Different amounts of gelatin structural order associated with a melting enthalpic change in the DSC measurement were prepared based on different gelatin drying conditions. Two consecutive heating and cooling DSC measurements on the gelatin films showed that there was no change in the glass‐transition temperature (Tg) for the amorphous gelatin but there was a decrease in the Tg for the structural gelatin on the second DSC scan. This decrease was attributed to the plasticizing effect from the release of originally hydrogen‐bonded water associated with the structural gelatin. In addition, a reversing endotherm observed upon melting of the structural gelatin during a temperature modulated DSC measurement indicated that the transition of bound water to free water occurred as the partial triple‐helix gelatin melted. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1795–1801, 2006 相似文献
994.
Polymers have been studied extensively because of their wonderful array of properties. Their properties can be tailored by many means and can be made useful in many ways. Polymers can be crosslinked or branched and can provide different properties, such as conduction and passivation. This study dealt with the RF sputter deposition of poly(tetrafluoroethylene) (PTFE) films with the aim of using them as masking materials during the fabrication of various micromachined structures. The films were deposited on silicon substrates at different plasma powers (100, 150, and 200 W) for a constant deposition time (60 min). To test the masking properties, the deposited films were immersed in a 20 wt % aqueous KOH solution at 80°C for 60 min. The films showed lower contact angles and interfacial tension, and this indicated good adhesion of the films to the silicon substrates. Good adhesion is an essential quality of masking materials during micromachining. The structural properties of the as‐deposited and etched films were studied with Fourier transform infrared and X‐ray photoelectron spectroscopy. These indicated that the bonding groups and binding energies of C? F and C? CF matched the reported values well. Furthermore, the presence of C? F and C? CF bonds, even after the etching of silicon substrates in highly alkaline KOH solutions for 60 min, showed that the PTFE films remained unchanged in the etchant and, therefore, could function as good masking materials during the fabrication of micromachined structures. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1183–1192, 2004 相似文献
995.
水溶液晶体的空间生长及其地基模拟实验 总被引:1,自引:0,他引:1
空间水溶液晶体生长是通过搭载人造卫星、宇宙飞船和空间站等飞行器,在微重力条件下从水溶液中进行晶体生长实验.许多透明单晶体,诸如:KDP(磷酸二氢钾,potassium dihydrogen phosphate)、ADP(磷酸二氢铵,ammonium dihydrogen phosphate)、TGS(硫酸三甘氨酸,triglycine sulfae)、沸石和α-碘酸锂(α-LiIO3)等无机非线性光学晶体,尿素等有机非线性光学晶体以及蛋白质等生物晶体,均可采用水溶液法生长.美国、前苏联、西欧和日本等国在从事空间材料科学研究的高科技发展计划中,均把水溶液晶体生长作为一项重要项目.由于水溶液晶体生长方法的研究在地面上已有丰富的基础,而且具有温度低,能耗小,可实现原位实时观察等优点,所以,它是探索空间晶体生长原理和方法、研究晶体生长微重力效应的重要材料制备技术.由于空间晶体生长受搭载条件限制,空间实验的次数与地面相比是十分稀少的,为了获得空间实验的高成功率,在地面上必须建立相应的实验基地,开展深入的地基研究工作.本文将分别从空间实验和地基研究两个方面作系列介绍,包括蛋白质晶体,沸石晶体,α-LiIO3晶体的空间生长以及TGS,NaClO3(sodium chlorate,氯酸钠),Sr(NO3)2(strontium nitrate,硝酸鍶)和Ba(NO3)2(barium nitrate,硝酸钡)等晶体生长过程的原位实时观察,并展望了空间晶体生长的发展前景. 相似文献
996.
We report the graft copolymerization of acrylic acid onto the polypropylene (PP) melt‐blown nonwovens induced by electron beam (EB) preirradiation in this article. The occurrence of the graft copolymerization was confirmed by means of XPS, FTIR, and SEM. The effects of preirradiation dose, monomer concentration, bath ratio, reaction time, and temperature on the graft ratio were investigated. The water conservation, water absorption rate, and K+ exchange capacity were also determined on the grafted PP melt‐blown nonwovens, which showed that EB preirradiation‐induced grafting was an effective way to improve the hydrophicility of PP melt‐blown nonwovens. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4971–4977, 2006 相似文献
997.
The key to the success of flip‐chip technology lies in the availability of sucessful underfill materials. However, the reliability of flip‐chip technology using current underfill materials is generally found to be lower than that of conventional wire‐bond connection packaging materials such as epoxy molding compound (EMC) because of the high coefficients of thermal expansion (CTE) and moisture absorption of cured underfill material. In this study desbimide (DBMI), which has a low melting point (about 80°C), was used in the underfill materials as a cohardener. As a result, DBMI‐added underfill can show excellent thermal reliability, which is due to the superior properties of the CTE, the elastic modulus, and water resistance. When the properties of a 2 wt % DBMI‐added underfill were compared with those of a typical underfill (epoxy/anhydride), the CTE value was reduced to less than one‐half at the solder reflow temperature (about 200°C), the elastic modulus was reduced to less than one‐half in the temperature region below the glass‐transition temperature, and the water resistance was improved twofold. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2617–2624, 2002 相似文献
998.
The heterogeneous phase transition of the organic vapours, cyclohexane and p-xylene, on a cold substrate was observed by cooling the substrate at a slow rate under reduced pressure conditions. Either organic vapour at a vapour pressure lower than 130 Pa formed directly solid crystals but p-xylene vapour at a higher vapour pressure formed liquid condensates with subsequent formation of solid crystals. The dependence of the critical supersaturation ratios on the critical temperatures and the physical properties of the organic vapours has been clarified by the equation derived on the basis of classical nucleation theory. 相似文献
999.
Interpenetrating polymer networks (IPNs) of glycerol modified castor oil polyurethane (GC‐PU) and poly(2‐ethoxyethyl methacrylate) poly(2‐EOEMA) were synthesized using benzoyl peroxide as initiator and ethylene glycol dimethacrylate (EGDM) as crosslinker. GC‐PU/poly (2‐EOEMA) interpenetrating polymer networks were obtained by transfer molding. The novel GC‐PU/poly (2‐EOEMA) IPNs are found to be tough films. These IPNs are characterized in terms of their resistance to chemical reagents thermal behavior (DSC, TGA) and mechanical behavior, including tensile strength, Young's modulus, shore A hardness, and elongation. The morphological behavior was studied by scanning electron microscopy. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1029–1034, 2004 相似文献
1000.
The effect of the reaction conditions on the grafting parameters during grafting of 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid onto sodium carboxymethylcellulose using H2O2/Fe+2 redox pair are studied at 30°C. The grafting ratio, add on, and conversion initially increase with the H2O2 concentration in the range of (10.0–15.0) × 10?2 mol dm?3. Thereafter, these parameters decrease with the H2O2 concentration. The grafting ratio, add on, and conversion increase when increasing the ferrous ion concentration from (0.5 to 4.0) × 10?2 mol dm?3 and decrease with a further increase in the concentration. It is observed that the grafting ratio and add on increase with the monomer concentration, whereas the conversion decrease. The hydrogen ions seem to be facilitating the grafting reaction up to a certain concentration and after this concentration seem to be retarding the process. The grafting ratio, add on, and conversion decrease with the sodium carboxymethylcellulose concentration. When increasing the time period from 60 to 90 min, the grafting parameters increase but decrease thereafter. Similarly, when increasing the temperature from 25 to 30°C, the grafting parameters increase and decrease thereafter. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4819–4825, 2006 相似文献