全文获取类型
收费全文 | 5970篇 |
免费 | 488篇 |
国内免费 | 841篇 |
专业分类
化学 | 2690篇 |
晶体学 | 26篇 |
力学 | 468篇 |
综合类 | 79篇 |
数学 | 2966篇 |
物理学 | 1070篇 |
出版年
2024年 | 11篇 |
2023年 | 67篇 |
2022年 | 108篇 |
2021年 | 142篇 |
2020年 | 161篇 |
2019年 | 173篇 |
2018年 | 163篇 |
2017年 | 164篇 |
2016年 | 200篇 |
2015年 | 172篇 |
2014年 | 274篇 |
2013年 | 455篇 |
2012年 | 271篇 |
2011年 | 309篇 |
2010年 | 267篇 |
2009年 | 377篇 |
2008年 | 404篇 |
2007年 | 405篇 |
2006年 | 388篇 |
2005年 | 311篇 |
2004年 | 300篇 |
2003年 | 278篇 |
2002年 | 269篇 |
2001年 | 229篇 |
2000年 | 247篇 |
1999年 | 154篇 |
1998年 | 156篇 |
1997年 | 132篇 |
1996年 | 124篇 |
1995年 | 117篇 |
1994年 | 90篇 |
1993年 | 72篇 |
1992年 | 61篇 |
1991年 | 50篇 |
1990年 | 31篇 |
1989年 | 15篇 |
1988年 | 25篇 |
1987年 | 24篇 |
1986年 | 20篇 |
1985年 | 16篇 |
1984年 | 18篇 |
1983年 | 5篇 |
1982年 | 4篇 |
1981年 | 7篇 |
1980年 | 8篇 |
1979年 | 9篇 |
1978年 | 7篇 |
1976年 | 5篇 |
1959年 | 1篇 |
1957年 | 1篇 |
排序方式: 共有7299条查询结果,搜索用时 0 毫秒
51.
Mao-fengZhang Qiao-hongYao Chun-huiHuang Wei-xiaoCao 《高分子科学》2005,(1):27-27
A kind of azo-containing resin (Azo-R) was synthesized by a simple way through the coupling reaction of 2-nitro-N-methyldiphenylamine-4-diazoresin (NDR) with phenol, and a new covalentely attached multilayer film from Azo-R as H-donor and photosensitive diazoresin, diphenylamine-4-diazoresin (DR) as H-acceptor via H-bonding attraction by selfassembly technique has been fabricated. Following the decomposition of diazonium group of DR under exposure to UV light, the H-bonds between the layers of the film convert to covalent bonds and the film becomes very stable toward polar solvents or electrolyte aqueous solutions. Thus the UV-irradiated azo-containing films can be used to measure photocurrent in a conventional three-electrode photoelectrochemical cell using KCl as supporting electrolyte. It was confirmed that the azo-containing multilayer film is responsible for the photocurrent generation. 相似文献
52.
Seto Y. Umemoto K. Arii T. Masuda Y. 《Journal of Thermal Analysis and Calorimetry》2004,76(1):165-177
New solid complex of nitrilotriacetic acid and bismuth trichloride was synthesized by a solid phase reaction of nitrilotriacetic
acid and bismuth trichloride at room temperature. The composition of the sample is BiCl3[N(CH2COOH)3]2.5. The crystal structure of the complex belongs to triclinic system with the lattice parameters: α=0.7849 nm, β=0.9821 nm,
χ=2.0021 nm, α=96.50°, β=98.76° and γ=90.49°. The far-infrared spectra show the bonding between the Bi ion and N atom of nitrilotriacetic
acid. The thermal analysis also demonstrates the complex formation between the bismuth ion and nitrilotriacetic acid. The
gaseous pyrolysis product and the final residue in the thermal decomposition process are determined to check the thermal decomposition
reaction.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
53.
Fang-Mo Chang Chen-Chia Huang Shin-Ming Shen Sun-I Chen 《Journal of Thermal Analysis and Calorimetry》1995,44(2):405-417
The effects of various burning rate catalysts on thermal decomposition of cured glycidyl azide polymer (GAP)-ammonium perchlorate (AP) propellants have been studied by means of thermal analysis and a modified vacuum stability test (MVST). Four types of iron-containing catalysts examined in this paper are catocene, ferrocenecarboxaldehyde (FCA), ferrocene, and ferric oxide. Results of differential thermal analysis (DTA) and thermogravimetric analysis (TG) revealed that the catalysts play an important role in the decomposition of both AP and GAP. The peak decomposition temperature (T m) of DTA curves and onset decomposition temperature (T o) of TG patterns considerably shifted to a lower temperature as the concentration of catalysts increased in the propellants. The endothermic temperature of AP, however, is unaffected by the presence of burning rate catalysts in all cases. The activation energy of decomposition of the propellants in range of 80 to 120°C is determined, based on the MVST results. 相似文献
54.
55.
The thermal decomposition of some M
2
I
HPO3 (M-Li, Na, K) phosphites under nitrogen atmosphere was investigated. A stepwise mechanism of thermal decomposition has been proposed.
Zusammenfassung Es wurde die thermische Zersetzung von Phosphiten M 2 I HPO3 (M-Li, Na, K) in Stickstoffatmosphere untersucht. Die Schritte des Mechanismus der thermischen Zersetzung wurden vorgeschlagen.相似文献
56.
SrO,MsO对异丙醇的分解反应有各自的作用形式,因而产物分布也有明显差别.MgO上异丙醇分解,在较低温度时,主要产物为丙酮和丙烯;随温度升高,生成丙烯的量增加,而丙酮的量减少,直至消失,在SrO上,异丙醇在较高温度时反应,产物几乎为丙酮,丙烯的生成量极少。认为:产物中丙烯来源于异丙醇在催化剂表面强酸中心上的脱水;丙酮在MgO上来源于强碱中心和酸中心协同作用异丙醇的脱氢,而在SrO上则是SrO表面极强的碱中心作用异丙醇而脱氢制得。 相似文献
57.
58.
设计合成了两种新型的以聚吡唑硼酸盐、氨基酸为配体的钒氧配合物VO[phCH2CH(NH2)COO][HB(pz)3](1)和VO(3,5-Me2pz)[HB(3,5-Me2pz)3](CH3COO)(2). 通过元素分析、红外光谱对配合物进行了表征, 并利用单晶X射线衍射技术解析了它们的结构. 非等温热分解动力学研究表明, 配合物1和2的热分解反应都是分两步进行的. 通过计算, 配合物1热分解的第一步反应的可能机理为成核与生长(n=1/4); 第二步反应的可能机理为化学反应. 其非等温动力学方程分别为, dα/dT=(A/β)e-E/RT(1/4)(1-α)[-ln(1-α)]-3 和dα/dT=(A/β)e-E/RT(1-α)2. 分解反应的表观活化能分别是223.52 和331.94 kJ·mol-1; 指前因子ln(A/s-1)分别是49.67 和57.50. 配合物2 热分解的第一步反应的可能机理为化学反应; 第二步反应的可能机理为成核与生长(n=1/2). 其非等温动力学方程分别为, dα/dT=(A/β)e-E/RT(1-α)2, 和dα/dT=(A/β)e-E/RT(1/2)(1-α)[-ln(1-α)]-1. 分解反应的表观活化能分别是300.56 和444.72 kJ·mol-1; 指前因子ln(A/s-1)分别是75.53 和92.50. 相似文献
59.
《Journal of separation science》2003,26(11):1057-1062
The use of glass fiber as a support material for a surface compound serving to generate gaseous standard mixtures of ethene is described. The technique is based on the process of thermal decomposition of the surface compound in a desorber connected on‐line via a multi‐port valve to the calibrated device. The surface compound undergoes thermal decomposition at 245°C, yielding known amounts of ethene. The method enables on‐line preparation of a standard mixture immediately before the calibration step. Consequently, it can be also applied for the generation of standard mixtures containing volatile, malodorous, unstable, and toxic compounds. 相似文献
60.