全文获取类型
收费全文 | 1259篇 |
免费 | 142篇 |
国内免费 | 1057篇 |
专业分类
化学 | 2235篇 |
晶体学 | 34篇 |
力学 | 13篇 |
综合类 | 16篇 |
物理学 | 160篇 |
出版年
2024年 | 8篇 |
2023年 | 16篇 |
2022年 | 50篇 |
2021年 | 65篇 |
2020年 | 81篇 |
2019年 | 56篇 |
2018年 | 74篇 |
2017年 | 54篇 |
2016年 | 88篇 |
2015年 | 69篇 |
2014年 | 75篇 |
2013年 | 129篇 |
2012年 | 121篇 |
2011年 | 81篇 |
2010年 | 87篇 |
2009年 | 88篇 |
2008年 | 96篇 |
2007年 | 91篇 |
2006年 | 110篇 |
2005年 | 103篇 |
2004年 | 105篇 |
2003年 | 97篇 |
2002年 | 73篇 |
2001年 | 73篇 |
2000年 | 67篇 |
1999年 | 65篇 |
1998年 | 65篇 |
1997年 | 73篇 |
1996年 | 63篇 |
1995年 | 59篇 |
1994年 | 51篇 |
1993年 | 51篇 |
1992年 | 27篇 |
1991年 | 11篇 |
1990年 | 12篇 |
1989年 | 5篇 |
1988年 | 7篇 |
1987年 | 2篇 |
1986年 | 2篇 |
1985年 | 5篇 |
1983年 | 2篇 |
1959年 | 1篇 |
排序方式: 共有2458条查询结果,搜索用时 15 毫秒
1.
This paper presents the importance and usage of natural zeolites, which was recently recognized in the industry. Therefore, the grinding properties of natural zeolite were studied with the emphasis on a kinetic study in a ball mill. The experimental mill employed was laboratory sized, 200 mm diameter, 191 mm length, providing a total mill volume of 6000 cm3, with a total mass of 5.62 kg of steel balls of 25 mm diameter with a charge of 20% of the mill volume and with a rotation speed of 76 rpm. The breakage parameters were determined by using single sized feed fractions of ?850+600 μm, ?600+425 μm, and ?425+300 μm for the zeolite samples. The Si (specific rate of breakage) and Bi, j (primary breakage distribution) values were obtained for those feed size fractions in order to predict the product size distributions by simulation for comparison to the experimental data. From the experimental results, Si values increased as the feed sizes became coarser, i.e., the highest Si value was 0.85 min?1 for ?850+600 μm, while the lowest Si value was 0.65 min?1 for ?425+300 μm feed ground in the mill. The Bi, j values obtained for the zeolite sample were γ=0.84, ?=0.61, and β=4.25. The breakage parameters obtained showed that the zeolite is broken faster than quartz and slower than calcite and barite in terms of the aT values reported previously at the same experimental conditions. The simulations of the product size distributions of zeolite were in good agreement with the experimental data using a standard ball mill simulation program. The slowing‐down effect was also seen in the mill after 4 min. of grinding. 相似文献
2.
Zeolite A rods by self-assembly of zeolite A microcrystal were successfully synthesized by microwave-assisted hydrotherrnal synthesis. The average size of zeolite crystals consisting of self-assembling materials was about 300 nm and the length of zeolite rods was in the range of 15--30μm. 相似文献
3.
H.-J. Sue E. I. Garcia-Meitin N. A. Orchard 《Journal of Polymer Science.Polymer Physics》1993,31(5):595-608
The fracture behavior of a core-shell rubber (CSR) modified epoxy is investigated using both fracture mechanics and microscopy tools. The CSR-modified epoxy is found to be toughened via numerous line-array cavitations of the CSR particles, followed by plastic flow of the epoxy matrix. The toughening effect via the above craze-like damage process is found to be as effective as that of the well-known widespread rubber cavitation/matrix shear yielding mechanisms. The conditions for triggering the craze-like damage appear to be both stress state and rubber concentration dependent. The type of rubber tougheners utilized also plays a critical role in triggering this rather unusual craze-like damage in epoxy systems. © 1993 John Wiley & Sons, Inc. 相似文献
4.
Tetraalkyltin complexes, SnR4 (R = Me, Et, Pr, Bu) could react with Pt/HY at 193, 243, 273 and 333 K, respectively. The reactions occurred on the surface of the zeolite and the organotin grafted zeolites were characterized in detail. The framework and the microporous structure of the grafted Pt/HY zeolites were retained. However, the modified zeolites showed better size selectivity in the absorption of hydrocarbons. 相似文献
5.
对水热处理后得到的USY沸石作进一步的酸处理以及采用改进的氟硅酸盐溶液骨架富硅工艺,分别得到了经XPS剖面分析证实为铝分布均匀的超稳Y沸石HAY-Ⅰ和HAY-Ⅱ。IR分析表明,在酸处理过程中从USY沸石中去掉的那部分非骨架铝类与3690cm~(-1)处羟基有关,仍残留在HAY-Ⅰ沸石中的那部分非骨架铝类与3670cm~(-1)和3600cm~(-1)处羟基有关。XRD和化学分析表明HAY-Ⅰ沸石仍含有约50%的非骨架铝类,而HAY-Ⅱ沸石则基本上不含非骨架铝类,HAY-Ⅱ沸石还显示更高的结晶保留度。DTA分析表明,HAY-Ⅰ和HAY-Ⅱ两种沸石的热稳定性均高于USY沸石。 相似文献
6.
H. L. Frisch Yongpeng Xue 《Journal of polymer science. Part A, Polymer chemistry》1995,33(12):1979-1985
A hybrid inorganic/organic interpenetrating polymer network (IPN) of a three-dimensional network structure zeolite crystal (13X, powder) and crosslinked or linear polystyrene (PS) was prepared and characterized by differential scanning calorimetry (DSC), solid-state13C-NMR, and scanning electron microscopy (SEM). The size and shape of the crystalline zeolite particles were revealed on SEM micrographs in both the pure zeolite and the IPNs. Solubility tests and the results of DSC with solid-state 13C-NMR confirm that some organic PS chains are incorporated within the internal three-dimensional channels of the zeolite particles. We speculate that the internal PS chains may adopt an extended “one-dimensional” conformation and exhibit no bulk polymer glass transition. These novel hybrid inorganic/organic IPNs are a new kind of IPN structure. © 1995 John Wiley & Sons, Inc. 相似文献
7.
T. G. Kuznetsova K. G. Ione N. F. Salakhutdinov 《Reaction Kinetics and Catalysis Letters》1997,62(2):273-280
The interaction of α-methacrolein with mixedtrans- andcis-alloocimenes on β zeolite has been studied at room temperature in a solvent under various conditions. The scheme of the process
has been specified including the formation of (4+2) and (3+2)-cycloaddition products and strongly adsorbed alloocimene species. 相似文献
8.
Xiujie Li Weiping Zhang Shenglin Liu Xiuwen Han Longya Xu Xinhe Bao 《Journal of molecular catalysis. A, Chemical》2006,250(1-2):94-99
The interfacial interaction of Mo species with the HBeta zeolite was studied by multinuclear MAS NMR, XRD and N2 adsorption. As proved by the quantitative 27Al MAS NMR, this interaction is so strong as to dealuminate the framework of HBeta, and leads to a new peak appearing at −14 ppm, which indicates the formation of crystalline Al2(MoO4)3. This can also be detected by XRD measurements when the Mo loading is as high as 9.0 wt.%. The corresponding quantitative 29Si and 1H MAS NMR spectra show that the amount of silanols and Brønsted acidic sites decrease obviously with increasing Mo loading. This also reveals an interaction between Mo species and HBeta support through an oxygen bridge resulting from condensation with the hydroxyls on the support. At higher Mo loadings, the interaction is so strong that it results in an extraction of aluminum from the zeolite framework, and subsequently appearance of Al2(MoO4)3 and loss of Brønsted acidic sites. These can be correlated to the low catalytic activity of Mo/HBeta in metathesis of ethylene and 2-butylene to propylene. 相似文献
9.
Rachel K. O'Reilly Maisie J. Joralemon Craig J. Hawker Karen L. Wooley 《Journal of polymer science. Part A, Polymer chemistry》2006,44(17):5203-5217
Block copolymer micelles and shell cross-linked nanoparticles (SCKs) presenting Click-reactive functional groups on their surfaces were prepared using two separate synthetic strategies, each employing functionalized initiators for the controlled radical polymerization of acrylate and styrenic monomers to afford amphiphilic block copolymers bearing an alkynyl or azido group at the α-terminus. The first route for the synthesis of the azide-functionalized nanostructures was achieved via sequential nitroxide-mediated radical polymerization (NMP) of tert-butyl acrylate and styrene, originating from a benzylic chloride-functionalized initiator, followed by deprotection of the acrylic acids, supramolecular assembly of the block copolymer in water and conversion of the benzylic chloride to a benzylic azide. In contrast, the second strategy utilized an alkynyl-functionalized reversible addition fragmentation transfer (RAFT) agent directly for the RAFT-based sequential polymerization of tetrahydropyran acrylate and styrene, followed by selective cleavage of the tetrahydropyran esters to give the α-alkynyl-functionalized block copolymers. These Click-functionalized polymers, with the functionality located at the hydrophilic polymer termini, were then self-assembled using a mixed-micelle methodology to afford surface-functionalized “Clickable” micelles in aqueous solutions. The optimum degree of incorporation of the Click-functionalized polymers was investigated and determined to be ca. 25%, which allowed for the synthesis of well-defined surface-functionalized nanoparticles after cross-linking selectively throughout the shell layer using established amidation chemistry. Functionalization of the chain ends was shown to be an efficient process under standard Click conditions and the resulting functional groups revealed a more “solution-like” environment when compared to the functional group randomly inserted into the hydrophilic shell layer. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5203–5217, 2006 相似文献
10.