全文获取类型
收费全文 | 7021篇 |
免费 | 752篇 |
国内免费 | 874篇 |
专业分类
化学 | 2683篇 |
晶体学 | 26篇 |
力学 | 460篇 |
综合类 | 79篇 |
数学 | 2966篇 |
物理学 | 1026篇 |
无线电 | 1407篇 |
出版年
2024年 | 18篇 |
2023年 | 90篇 |
2022年 | 119篇 |
2021年 | 177篇 |
2020年 | 208篇 |
2019年 | 198篇 |
2018年 | 193篇 |
2017年 | 208篇 |
2016年 | 245篇 |
2015年 | 246篇 |
2014年 | 373篇 |
2013年 | 547篇 |
2012年 | 399篇 |
2011年 | 401篇 |
2010年 | 338篇 |
2009年 | 440篇 |
2008年 | 466篇 |
2007年 | 473篇 |
2006年 | 448篇 |
2005年 | 340篇 |
2004年 | 339篇 |
2003年 | 312篇 |
2002年 | 299篇 |
2001年 | 253篇 |
2000年 | 266篇 |
1999年 | 163篇 |
1998年 | 168篇 |
1997年 | 145篇 |
1996年 | 137篇 |
1995年 | 130篇 |
1994年 | 101篇 |
1993年 | 78篇 |
1992年 | 66篇 |
1991年 | 53篇 |
1990年 | 36篇 |
1989年 | 15篇 |
1988年 | 25篇 |
1987年 | 24篇 |
1986年 | 20篇 |
1985年 | 17篇 |
1984年 | 21篇 |
1983年 | 6篇 |
1982年 | 4篇 |
1981年 | 9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8647条查询结果,搜索用时 15 毫秒
111.
Thermal decomposition of transition metal malonates, MCH2C2O4?xH2O and transition metal succinates, M(CH2)2C2O4?xH2O (M=Mn, Fe, Co, Ni, Cu, Zn) has been studied employing TG, DTG, DTA, XRD, SEM, IR and Mössbauer spectroscopic techniques. After dehydration, the anhydrous metal malonates and succinates decompose directly to their respective metal oxides in the temperature ranges 310–400 and 400–525°C, respectively. The oxides obtained have been found to be nanosized. The thermal stability of succinates have been found to be higher than that of the respective malonates. 相似文献
112.
Cu,Pd-ZSM-5上NO分解和CO氧化的催化作用 总被引:4,自引:0,他引:4
双交换Cu,pd-ZSM-5催化剂(Cu交换度为105%,Pd交换度分别为3.4%和33%)对CO氧化反应有活性增强作用,对NO分解反应不存在增强效应.双交换催化剂在于交换程序不同,而表面物种不同,活性组分的分布状态不同,因而有不同的活性.先交换Cu,400℃焙烧后再交换pd的Cu-Pd-ZSM-5催化剂,对上述两类反应的活性存双组分催化剂中均为最高.H_2-TPR谱表明,共交换的Cu-Pd-ZSM-5中尚有部分CuCl+占据了部分交换位置,而使CO氧化活性稍有下降.N_2-DTA和H_2-TPR谱结果表明,Pd交换到Cu-ZSM-5中后,抑制了吸附水和水合铜化合物的形成,由此提高了在200—300℃时氧的吸附量.后者的大小和CO氧化活性有顺变关系.N_2-DTA谱中340—445℃的放热峰可能分别表征了和NO分解活性有关的铜氧桥或把氧桥的形成,该放热峰的峰温愈低,峰面积愈大,则NO分解活性愈高. 相似文献
113.
本工作用四种较新的质谱技术(碰撞诱导解离(CID),电荷剥离(CS),电荷分离(CSe),电子捕获诱导解离(ECID)谱研究了邻、间、对溴甲苯和溴化苄四种异构体。四种技术在一定程度上都可区分这些异构体。其中比较四种异构体ECID谱中ECID峰的相对强度可得到满意的区分效果。 相似文献
114.
A new technique, called modulated thermogravimetry, is introduced as a tool for obtaining continuous kinetic information for
decomposition and volatilization reactions. The approach makes use of an oscillatory temperature program to obtain kinetic
parameters during a mass loss. MTGA™ may be used under quasi-isothermal conditions to observe a single mass loss or may be
combined with linear heating rate or Hi-Res™ controlled rate thermogravimetry to scan from one mass loss region to another.
Results obtained are in agreement with those obtained by other kinetic methods.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
115.
Summary {\rtf1\ansi\ansicpg1250\deff0\deflang1038\deflangfe1038\deftab708{\fonttbl{\f0\froman\fprq2\fcharset238{\*\fname Times New Roman;}Times New Roman CE;}}
\viewkind4\uc1\pard\f0\fs20 New explanations are given for two types of irregular thermogravimetric (TG) data. A TG relationship between mass and temperature is derived on the basis of migration behavior of bubbles generated in bulk of sample system, and superposed on that derived on the basis of kinetics of the 4\super th\nosupersub order event, which is superposed on the experimental TG data obtained from three reference papers. This suggests that these TG data are reflecting migration of bubbles. A dependence of TG behavior on heating rate, which is contrary to usual that, is shown and is explained in terms of event-rate determination by boiling.
\par } 相似文献
116.
The thermal decomposition characteristics of1,7-diazido-2,4,6-trinitrazaheptane (DATH) and multi-component systems containing
DATH were studied by using DSC, TG and DTG techniques. Three –NO2 groups in the DATH molecule break away first from the main chain when DATH is heated up to 200°C. Following this process,
the azido groups and the residual molecule decompose rapidly to release a great deal of heat within a short time. In the multi-component
systems, DATH undergoes a strong interaction with the binder of the double-base propellant and a weak interaction with RDX.
The burning rates of the two propellants were determined by using a Crawford bomb. The results showed that the burning rate
rises by about 19–66% when 23.5%DATH is substituted for RDX in a minimum smoke propellant. Meanwhile, the N2 level in the combustion gases is enhanced, which is valuable for a reduction of the signal level of the solid propellant.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
117.
The synthesis of malachite CuCO3·Cu(OH)2 or Cu2CO3(OH)2 was studied through titrations of copper(II) salt solutions with a solution of sodium carbonate at different temperatures. The precipitates were characterized by TG, IR and chemical analysis. The composition varies depending on thepH of the solution and the temperature. Purer malachite was synthesized by simple mixing of a solution of copper(II) nitrate or sulfate with a solution of sodium carbonate at 50°C.The kinetics of the thermal decomposition of synthetic malachite was described by eitherR
3 orA
m(m=1.2–1.4) law, according to TG analysis, both isothermal and nonisothermal. The Arrhenius parameters determined using three different integral methods showed the kinetic compensation effect, which is correlated to the working temperature interval analyzed.The authors thank Mr. H. Takemoto for analyzing kinetics of the thermal decomposition of synthetic malachite. 相似文献
118.
119.
120.
B. Kowalczyk 《Journal of Thermal Analysis and Calorimetry》2000,60(1):163-166
The comparison of thermal and calorimetric properties of metal derivatives of 6-aminopicolinic acid (APH) is presented. The
salts and complexes of APH with Cr(III), Cd(II), Cu(II), Ni(II), Pb(II), Co(II)and Ag(I) have been studied by TG-DTA and DSC
methods up to 1200°C in a nitrogen atmosphere. Decomposition processes are proposed. The decarboxylation, deamination and
carbonation of the organic fragments of molecules take place. The compounds decompose to metal or to metal oxides. The values
of the transition enthalpy were determinated.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献