全文获取类型
收费全文 | 13612篇 |
免费 | 1162篇 |
国内免费 | 604篇 |
专业分类
电工技术 | 829篇 |
技术理论 | 1篇 |
综合类 | 825篇 |
化学工业 | 2125篇 |
金属工艺 | 864篇 |
机械仪表 | 778篇 |
建筑科学 | 954篇 |
矿业工程 | 371篇 |
能源动力 | 435篇 |
轻工业 | 843篇 |
水利工程 | 245篇 |
石油天然气 | 770篇 |
武器工业 | 92篇 |
无线电 | 1721篇 |
一般工业技术 | 1651篇 |
冶金工业 | 842篇 |
原子能技术 | 178篇 |
自动化技术 | 1854篇 |
出版年
2024年 | 81篇 |
2023年 | 207篇 |
2022年 | 347篇 |
2021年 | 514篇 |
2020年 | 386篇 |
2019年 | 338篇 |
2018年 | 413篇 |
2017年 | 435篇 |
2016年 | 388篇 |
2015年 | 492篇 |
2014年 | 646篇 |
2013年 | 711篇 |
2012年 | 805篇 |
2011年 | 838篇 |
2010年 | 734篇 |
2009年 | 736篇 |
2008年 | 729篇 |
2007年 | 740篇 |
2006年 | 727篇 |
2005年 | 624篇 |
2004年 | 409篇 |
2003年 | 475篇 |
2002年 | 463篇 |
2001年 | 406篇 |
2000年 | 382篇 |
1999年 | 382篇 |
1998年 | 359篇 |
1997年 | 325篇 |
1996年 | 319篇 |
1995年 | 215篇 |
1994年 | 179篇 |
1993年 | 132篇 |
1992年 | 100篇 |
1991年 | 87篇 |
1990年 | 69篇 |
1989年 | 47篇 |
1988年 | 33篇 |
1987年 | 26篇 |
1986年 | 20篇 |
1985年 | 12篇 |
1984年 | 11篇 |
1983年 | 9篇 |
1982年 | 8篇 |
1981年 | 4篇 |
1980年 | 5篇 |
1979年 | 3篇 |
1973年 | 2篇 |
1972年 | 1篇 |
1971年 | 1篇 |
1970年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
91.
移动计算环境中带宽具有非对称性,并且移动设备资源有限,传统的缓存管理策略需要占用大量的设备计算资源和网络带宽,有效的缓存管理技术能够极大提高移动计算的性能。对此提出一系列的针对移动计算的缓存管理策略。首先根据用户访问频率建立对应的具有生命周期的数据项缓存,然后使用自适应一致性维护策略维护缓存的一致性。通过实验分析,提出的管理策略能够很好地降低带宽占用,并且有效地减少对移动客户端的资源需求。 相似文献
92.
聚苯乙烯/聚乙烯塑料合金的研究 总被引:6,自引:0,他引:6
以氢化SBS(SEBS)为相容剂,对聚苯乙烯/聚乙烯塑料合金进行了研究,着重讨论了体系中组成、相容剂含量、PS分子量以及合金制备条件对合金结构与性能的影响。 相似文献
93.
捣固炼焦在中国焦化工业发展中的前景与展望 总被引:5,自引:0,他引:5
介绍了我国炼焦煤源的现状、捣固炼焦的理论依据,并将捣固炼焦技术与常规炼焦方法进行了比较,指出捣固炼焦应向大型化方向发展,并提高捣固和装煤的自动化水平,发展捣固炼焦可促进我国焦化工业的可持续发展。 相似文献
94.
Novel silica nanoboxes were prepared by controlled dealumination of Na-X and Ca-A type zeolites using ammonium hexafluorosilicate (AHFS). The silica-richer
the parent zeolite, the smaller the average pore size produced and the narrower the pore size distribution obtained. This
was due to the specific reactivity of the extracting agent with the zeolite framework aluminum atoms. High temperature calcination
of the dealuminated X-zeolite (ammonium form) resulted in mesoporous materials exhibiting an ink-bottle shape, a quite high
surface area (330 m2/g, no micropores), an average pore diameter of 4.5 nm with a quite narrow pore size distribution (± 1.0 nm) and finally,
a pore opening diameter of 3.9 nm. The latter was determined by using the nitrogen sorption isotherms (BET technique) and
related pore volume data. The sorption behavior also suggested the interconnecting character of the newly created nanoboxes. The periodicity of these nanoboxes throughout the mesoporous material was clearly shown by X-ray powder diffraction at very small angles.
These materials, herein called monomodal nanoboxes because of the absence of micropores in the structure, were also thermally stable. Incorporation of orthosilicate into the obtained silica nanoboxes, in accordance with the recently developed technique for
pore size engineering in zeolites, led to materials with smaller pore openings but having almost the same textural properties. Solid superacidic materials were prepared by incorporating a liquid superacid
(triflic acid or trifluoromethanesulfonic acid) into the silica nanoboxes using the wet impregnation technique. The maximum
triflic acid loading which did not significantly affect the mesoporous framework of the materials was 24 wt%. As a reference,
the maximum loading of less acidic sulfuric acid was slightly lower. All this showed the high chemical stability of the silica nanoboxes for supporting very acidic species. Temperature-programmed desorption using a combined DTA/TGA system
allowed the identification of the bound phases and some liquid phase of the loaded triflic acid. 相似文献
95.
96.
Wen‐Bin Liau Yu‐Ting Sun Ling‐Yueh Yang Lee‐Yih Wang Wen‐Yen Chiu Kuo‐Huang Hsieh Sheng‐Mao Tseng 《应用聚合物科学杂志》2006,102(6):5406-5413
The polyaniline (PANI)‐coated polystyrene (PS) latexes were synthesized, and the electrically conductive films were prepared thereafter. The weight ratio of PANI was 5%. Thermal analysis of the latices was performed using DSC and TGA. In this study, the electrically conductive films were prepared above the PS glass transition temperature (Tg). During the film formation, the effects of the annealing temperature and atmosphere (air or N2) on the film resistance were investigated. In addition, the film morphology was observed utilizing scanning electron microscopy. The film resistance decreased in the initial heating stage due to the increasing temperature and the compaction of film. Then the film resistance increased with further annealing due to the aging of PANI. Typically, the film resistance was about 6000 Ω/sq, and the conductivity was 0.3 S/cm. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5406–5413, 2006 相似文献
97.
It is shown that even pure quartz, other silicas or aluminas can enhance the aromatization activity of a ZSM-5 zeolite. Incorporation of gallium oxide onto these supports increases further the production of aromatics. The use of supported gallium oxide co-catalyst obtained by co-evaporation of a colloidal silica and a Ga salt has led to extremely high aromatization performance for the hybrid catalyst. 相似文献
98.
Changes in the crystal morphology, crystallinity, and the melting temperature of thermoplastics resulted in significant changes in the mechanical behavior of composites containing them. For this reason, the research of crystal morphology and crystallization kinetics in thermoplastic composites became an important requirement. The thermoplastic filled with the filler of different size gradation was a new method for improving processability of thermoplastic composites. We have previously reported that the melt viscosity of polypropylene (PP) composites, which were filled with 30 wt % CaCO3 of effective size gradation, could be evidently declined. In this study, two sizes of CaCO3, 325 meshes and 1500 meshes, were blended by different proportions and filled into PP matrix with 30 wt %. Crystal morphology and isothermal crystallization kinetics of a series of composites were characterized by differential scanning calorimeter (DSC) and polarizing microscope. The results showed that composites filled with CaCO3 of effective size gradation leaded to a well‐crystalline order and a large crystal size, while their isothermal crystallization kinetics and crystallization rate constant (k) were declined, and their Avrami exponents (n) and crystallization half‐life (t1/2) were increased compared with the composites filled with single size CaCO3. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2437–2444, 2006 相似文献
99.
聚合物流变性能对共注射成型的影响 总被引:3,自引:0,他引:3
在共注射成型多相分层流动充模成型机理的基础上,揭示了芯壳层熔体对共注射成型的分层界面形貌和芯层熔体前沿突破的影响,并模拟了芯壳层熔体粘度比对共注射成型的影响,建立了芯壳层熔体粘度与分层界面和前沿移动界面菜貌的关系。本文的模拟研究结果与一些文献的实验结果相吻合。 相似文献
100.
The melt intercalation method was employed to prepare poly(butylene terephthalate) (PBT)/montmorillonite (MMT) nanocomposites, and the microstructures were characterized with X‐ray diffraction and transmission electron microscopy. Then, the nonisothermal crystallization behavior of the nanocomposites was studied with differential scanning calorimetry (DSC). The DSC results showed that the exothermic peaks for the nanocomposites distinctly shifted to lower temperatures at various cooling rates in comparison with that for pure PBT, and with increasing MMT content, the peak crystallization temperature of the PBT/MMT hybrids declined gradually. The nonisothermal crystallization kinetics were analyzed by the Avrami, Jeziorny, Ozawa, and Mo methods on the basis of the DSC data. The results revealed that very small amounts of clay (1 wt %) could accelerate the crystallization process, whereas higher clay loadings reduced the rate of crystallization. In addition, the activation energy for the transport of the macromolecular segments to the growing surface was determined by the Kissinger method. The results clearly indicated that the hybrids with small amounts of clay presented lower activation energy than PBT, whereas those with higher clay loadings showed higher activation energy. The MMT content and the crystallization conditions as well as the nature of the matrix itself affected the crystallization behavior of the hybrids. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3257–3265, 2006 相似文献