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排序方式: 共有97条查询结果,搜索用时 15 毫秒
1.
Changjun Peng Shouhong Xu Hongze Gang Tianxiang Yin Jun Hu Yazhuo Shang Honglai Liu Encheng Hei 《大学化学》1986,36(1):2006013-0
As a necessary basic theory course for undergraduates majoring in chemistry, materials, pharmacy, chemical engineering, and biology, physical chemistry plays an important role in cultivating talents to meet the needs of social and economic development. Over the years, the teaching team of physical chemistry of East China University of Science and Technology has carried out the curriculum reform and innovation persistently based on "Team building as the foundation, resource building as the root, mode innovation as the soul, ability training as the origin". This paper will summarize our thinking and experience in striving for the first-class course from the aspects of first-class team construction, first-class resource construction, teaching connotation innovation, teaching mode exploration, and extract the experience that can be used as reference by teaching peers. 相似文献
2.
Xin-ping Duan Tianyi Chen Tianxiang Chen Lele Huang Li Ye Benedict T. W. Lo Youzhu Yuan Shik Chi Edman Tsang 《Chemical science》2021,12(25):8791
Coinage metal nanoparticles with high dispersion can serve as highly efficient heterogeneous catalysts. However, owing to their low melting point, poor thermal stability remains a major obstacle towards their application under reaction conditions. It is a common practice to use porous inorganic templates such as mesoporous silica SBA-15 to disperse Ag nanoparticles (NPs) against aggregation but their stability is far from satisfactory. Here, we show that the catalytic activity for hydrogenation of dimethyl oxalate (DMO) to methyl glycolate (MG) over Ag NPs dispersed on SBA-15 silica can be further promoted by incorporation of alkali metal ions at small loading, which follows the inverse order of their cationic size: Li+ > Na+ > K+ > Rb+. Among these, 5Ag1–Li0.05/SBA-15 can double the MG yield compared to pristine 5Ag/SBA-15 under identical conditions with superior thermal stability. Akin to the effect of an ionic surfactant on stabilization of a micro-emulsion, the cationic charge of an alkali metal ion can maintain dispersion and modulate the surface valence of Ag NPs. Interstitial Li in the octahedral holes of the face center packed Ag lattice is for the first time confirmed by X-ray pair distribution function and electron ptychography. It is believed that this interstitial-stabilization of coinage metal nanoparticles could be broadly applicable to multi-metallic nanomaterials for a broad range of C–O bond activating catalytic reactions of esters.Coinage metal nanoparticles with high dispersion can serve as highly efficient heterogeneous catalysts. 相似文献
3.
Yunqing Han Tianxiang Li Kozo Saito 《Journal of Thermal Analysis and Calorimetry》2013,112(2):683-687
The application of the average linear integral isoconversional method developed by Ortega for evaluating the activation energies of solid state reactions may be hindered by experimental noise and the uncertainties associated with selecting appropriate reaction segments. This paper suggests a procedure, called the modified Ortega method, which can avoid or minimize these hindrances. By applying the modified Ortega method to the kinetic analyses of both simulated and experimental data, a more consistent dependence of the activation energy on the extent of reaction conversion was found with those calculated from the modified Vyazovkin method and the Friedman method. 相似文献
4.
Wei Xu Dr. Karoly Kozma Tianxiang Sha Yi-Jen Wu Prof. May Nyman Prof. Michael M. Lerner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(36):8101-8104
The alkaline earth metals (M=Mg, Ca, Sr, and Ba) exhibit a +2 oxidation state in nearly all known stable compounds, but MI dimeric complexes with M−M bonding, [M2(en)2]2+, (en=ethylenediamine) of all these metals can be stabilized within the galleries of donor-type graphite intercalation compounds (GICs). These metals can also form GICs with more conventional metal (II) ion complexes, [M(en)2]2+. Here, the facile interconversion between dimeric-MI and monomeric-MII intercalates upon the addition/removal of en are reported. Thermogravimetry, powder X-ray diffraction, and pair distribution function analysis of total scattering data support the presence of either [M2(en)2]2+ or [M(en)2]2+ guests. This phase conversion requires coupling graphene and metal redox centers, with associated reversible M−M bond formation within graphene galleries. This chemistry allows the facile isolation of unusual oxidation states, reveals M0→M2+ reaction pathways, and present new opportunities in the design of hybrid conversion/intercalation materials for applications such as charge storage. 相似文献
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Stochastic resonance (SR) in an over-damped linear system subjected to an excitation of bias signal modulated noise with multiplicative and additive noises is investigated. We obtain the exact expressions of the first two moments and the signal-to-noise ratio (SNR) of the output by using linear-response theory. The SNR depends non-monotonically on the intensity and the correlation time of multiplicative noise, the correlation time of additive noise, the intensity of the cross noise between multiplicative and additive noise, as well as the external field frequency. The conventional SR, the SR in a broad sense and the bona fide SR are found in the system. The influences of the asymmetries of multiplicative and additive noise, the correlation rate of the cross noise, the intensity of additive noise, the amplitude of signal and the bias on the SNR are analyzed. Moreover, we pointed out that SR can be realized by tuning the system parameter with fixed noise, i.e., parameter-induced stochastic resonance (PSR) exists. 相似文献
8.
Hongmei Qin Lisheng Li Tianxiang Liang Xiaobin Peng Junbiao Peng Yong Cao 《Journal of polymer science. Part A, Polymer chemistry》2013,51(7):1565-1572
Four new donor–acceptor (donor) [D–A(D)], PBDT‐PTQ, PBDT‐PTTQ, PBDT‐TQ, and PBDT‐TTQ, bearing the same backbone of alternative benzodithiophene (BDT) and quinoxaline units but with phenylene thienyl, phenylene di‐thienyl, thienyl and di‐thienyl groups (other donors), respectively, at the acceptor quinoxaline units, were designed and synthesized to investigate the impacts of the conjugated side chains at the acceptor units on the photovoltaic properties of polymers. The power conversion efficiencies (PCEs) of the polymer solar cells (PSCs) based on PBDT‐TQ:[6,6]‐phenyl‐C‐70‐butyric acid methyl ester (PC70BM) and PBDT‐PTQ:PC70BM reach to 4.39 and 3.58%, respectively, which are 43 and 17% higher, respectively, than that of a reported alkylphenyl substituted polymer with the same main chain. However, the PCEs based on PBDT‐TTQ and PBDT‐PTTQ, in which an additional thiophene is added at a side chain of PBDT‐TQ and PBDT‐PTQ, respectively, decline. The mechanism how the conjugated side chains affect the performance of the PSCs is also discussed. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
9.
塔里木河干流区地方性氟病区水化学成分的多元分析 总被引:2,自引:0,他引:2
本文运用相关分析、回归分析及R-型系统聚类分析等方法,研究了里木河干流地区的地方性氟中毒病区内,氟斑牙患病率与饮用水中氟元素及其它化学成分的定量关系,并建立了生活饮用水中氟元素与其它化学成分的回归计算模型,提示了区域内氟斑牙治病的主导因素以及水体中各化学成分和化学性质指标间的相互关系,为探求饮用水型地方性氟中毒的病因提供了科学依据。 相似文献
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