全文获取类型
收费全文 | 101篇 |
免费 | 11篇 |
专业分类
化学 | 77篇 |
数学 | 1篇 |
物理学 | 34篇 |
出版年
2023年 | 1篇 |
2021年 | 1篇 |
2020年 | 5篇 |
2019年 | 3篇 |
2018年 | 2篇 |
2017年 | 1篇 |
2016年 | 5篇 |
2015年 | 4篇 |
2014年 | 4篇 |
2013年 | 6篇 |
2012年 | 10篇 |
2011年 | 7篇 |
2010年 | 1篇 |
2009年 | 2篇 |
2008年 | 3篇 |
2007年 | 3篇 |
2006年 | 8篇 |
2005年 | 5篇 |
2004年 | 1篇 |
2003年 | 2篇 |
2002年 | 1篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1997年 | 1篇 |
1996年 | 2篇 |
1995年 | 1篇 |
1994年 | 5篇 |
1993年 | 3篇 |
1992年 | 5篇 |
1991年 | 4篇 |
1989年 | 2篇 |
1988年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1980年 | 2篇 |
1976年 | 1篇 |
排序方式: 共有112条查询结果,搜索用时 31 毫秒
101.
102.
103.
104.
Dr. Guoju Yang Dr. Sneha A. Akhade Xi Chen Dr. Yue Liu Dr. Mal‐Soon Lee Dr. Vassiliki‐Alexandra Glezakou Dr. Roger Rousseau Prof. Dr. Johannes A. Lercher 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(11):3565-3570
The thermodynamic state of H2 adsorbed on Pt in the aqueous phase was determined by kinetic analysis of H2 reacting with D2O to HDO, HD, and D2, and by DFT‐based ab initio molecular dynamics simulations of H2 adsorption on Pt(111), Pt(110), and Pt nanoparticles. Dissociative adsorption of H2 on Pt is significantly weakened in the aqueous phase compared to adsorption at gas–solid interfaces. Water destabilizes the adsorbed H atoms, decreasing the heat of adsorption by 19–22 kJ while inducing an additional entropy loss of 50–70 J K?1. Upon dissociative adsorption of H2, the average distance of water from the Pt surface increases and the liquid adopts a structure that is more ordered than before close to the Pt surface, which limits the translation mobility of the adsorbed H atoms. The presence of hydrated hydronium ions next to the Pt surface further lowers the H?Pt bond strength. 相似文献
105.
Microwave heating of ceramic composites 总被引:1,自引:0,他引:1
The microwave heating of a ceramic composite is modelled andanalysed. The composite consists of many small ceramic particlesembedded in a ceramic cement. The composite is assumed to bewell insulated, and each particle is assumed to be in imperfectthermal contact with the surrounding cement. Based on thesetwo assumptions an asymptotic theory exploiting the small Biotnumber and small non-dimensional contact conductance is developed.Our asymptotic theory yields a set of nonlinear partial differentialequations which govern the temperature in the composite. Theseare reduced to a set of coupled nonlinear ordinary differentialequations in which the surface area of each particle entersas a parameter. Recent experiments with such composites haveshown that the steady-state temperature of the composite isstrongly dependent upon the radii of the embedded particles.Our model captures this effect. In fact, our analysis showsthat the assumption of imperfect thermal contact between theparticles and the ceramic cement is essential for this trendto be established. 相似文献
106.
107.
108.
ICP-AES法测定色漆可溶性金属含量 总被引:1,自引:0,他引:1
用ICP-AES法测定了色漆中的“可溶性”金属铬、镉、铅元素,考察了不同酸度对分析结果的影响,优化了测试条件。进行了回收率和精密度试验。并用原子吸收光谱国标方法进行对照,结果一致。 相似文献
109.
In situ S K-edge XANES experiments were carried out on second-generation SO(x)() trapping materials under oxidizing and reducing conditions. The experiments clearly show that the strong release of SO(2) under rich conditions at plug flow conditions is caused by the facilitated reduction of sulfite species on Pt. In the absence of Pt the sulfite species were stable under reducing conditions, while maintaining a similar total SO(2) uptake capacity. Thus, SO(x)() trapping materials without a noble metal are a clearly better option. The enhancing effect on the SO(x)() storage process of water present in the gas mixture is attributed to the formation of a higher sulfate fraction in the samples. The application of the in situ S K-edge XANES technique clearly reveals new information and insights on the behavior of the sulfur in the trapping process compared to that from the ex situ measurements and is therefore essential for designing new SO(x)() trapping materials. 相似文献
110.
Dr. Meng Wang Yuntao Zhao Prof. Dr. Donghai Mei Dr. R. Morris Bullock Dr. Oliver Y. Gutiérrez Dr. Donald M. Camaioni Prof. Dr. Johannes A. Lercher 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(4):1461-1465
The hydrogenolysis of the aromatic C−O bond in aryl ethers catalyzed by Ni was studied in decalin and water. Observations of a significant kinetic isotope effect (kH/kD=5.7) for the reactions of diphenyl ether under H2 and D2 atmosphere and a positive dependence of the rate on H2 chemical potential in decalin indicate that addition of H to the aromatic ring is involved in the rate-limiting step. All kinetic evidence points to the fact that H addition occurs concerted with C−O bond scission. DFT calculations also suggest a route consistent with these observations involving hydrogen atom addition to the ipso position of the phenyl ring concerted with C−O scission. Hydrogenolysis initiated by H addition in water is more selective (ca. 75 %) than reactions in decalin (ca. 30 %). 相似文献