全文获取类型
收费全文 | 5786篇 |
免费 | 398篇 |
国内免费 | 605篇 |
专业分类
化学 | 2959篇 |
晶体学 | 25篇 |
力学 | 256篇 |
综合类 | 67篇 |
数学 | 537篇 |
物理学 | 618篇 |
综合类 | 2327篇 |
出版年
2024年 | 17篇 |
2023年 | 63篇 |
2022年 | 139篇 |
2021年 | 120篇 |
2020年 | 136篇 |
2019年 | 143篇 |
2018年 | 116篇 |
2017年 | 168篇 |
2016年 | 170篇 |
2015年 | 167篇 |
2014年 | 251篇 |
2013年 | 308篇 |
2012年 | 373篇 |
2011年 | 344篇 |
2010年 | 234篇 |
2009年 | 310篇 |
2008年 | 382篇 |
2007年 | 373篇 |
2006年 | 371篇 |
2005年 | 347篇 |
2004年 | 312篇 |
2003年 | 263篇 |
2002年 | 225篇 |
2001年 | 197篇 |
2000年 | 161篇 |
1999年 | 161篇 |
1998年 | 133篇 |
1997年 | 128篇 |
1996年 | 102篇 |
1995年 | 93篇 |
1994年 | 94篇 |
1993年 | 85篇 |
1992年 | 58篇 |
1991年 | 67篇 |
1990年 | 46篇 |
1989年 | 41篇 |
1988年 | 17篇 |
1987年 | 12篇 |
1986年 | 8篇 |
1985年 | 6篇 |
1984年 | 9篇 |
1983年 | 6篇 |
1982年 | 12篇 |
1981年 | 8篇 |
1980年 | 2篇 |
1979年 | 5篇 |
1978年 | 3篇 |
1974年 | 2篇 |
1936年 | 1篇 |
排序方式: 共有6789条查询结果,搜索用时 15 毫秒
71.
Qingde Zhang Yisheng Tan Caihong Yang Yizhuo Han Jun Shamoto Noritatsu Tsubaki 《天然气化学杂志》2007,16(3):322-325
The attractive utilization route for one-step catalytic oxidation of dimethyl ether to dimethoxymethane was successfully carried out over the H3PW12O40(40%)/SiO2 catalyst, modified by Cs, K, Ni, and V. The Cs modification of H3PW12O40(40%)/SiO2 gave the most promising result of 20% dimethyl ether conversion and 34.8% dimethoxymethane selectivity. Dimethoxymethane could be synthe- sized via methoxy groups decomposed from dimethyl ether through the synergistic effect between the acid sites and the redox sites of Cs modified H3PW12O40(40%)/SiO2. 相似文献
72.
73.
将改进的基本度量理论与热力学微扰理论相结合,提出了胶体/高分子系统排空相互作用的IRDFT理论。该理论解释了在实际胶体系统中起重要作用的排斥体积效应和高分子链内相关性的竞争机制。应用该IRDFT,分别以线性链状和环状结构的高分子及其单体为排空元,计算了不同排空元条件下的胶体间排空相互作用。研究表明:对于絮凝破坏,自由环状高分子具有更大的优势。 相似文献
74.
75.
QIAN Baogong 《高分子科学》1988,(2):97-116
For the mechanism of isothermal bulk crystallization of high polymers, beside the nucleation and growth steps, the unimpingement of growing crystal aggregates should be taken into account for the modification of the Avrami equation. Starting from Poisson distribution function of growing crystal aggregates, the probability of the unimpinging ones should be P(0)+P(1), then the Q-modified Avrami equation thus derived can be expressed aswhere V0 represents the volume fraction of crystal aggregates at crystallization time t at a given temperature, while the exponent n on t relates to the mode of nucleation and growth, and K_q is the corresponding shape factor. This Q-modified one is verified satisfactory by the isothermal bulk crystallization of lanthanidecatalytically polymerized polybutadiene (Ln-PB), polyisoprene (Ln-PIR) and their copolymers (LnPB/IR). Furthermore, the proposed mechanism is well identified by the change of morphological state during the course of crystallization of the corresponding east film of Ln-PB TR (92/8) at-60°(Fig. 1).Upon examination of the influence of the number of entanglement on crystallization rate, it reveals the existence of two stages of entanglementation, the primary and the secondary ones (Fig. 19)The equation for dependence of molecular weight and entanglement on bulk crystallization rate has been derived as Eq. 13 or 18 for Ln-PB, and verified by the experimental rate data of well fractionated Ln-PB samples crystallized at -9.1 to -15℃(Fig.20). 相似文献
76.
Yagi Kiyohito Hamada Kenji Hlrata Kazumasa Miyamoto Kazuihisa Miura Yoshiharu Akano Tohru Fukatu Kiyomi Ikuta Yoshiaki Nakamura Hiroshi K. 《Applied biochemistry and biotechnology》1994,(1):225-232
A marine green alga,Chlamydomonas sp. strain MGA161 was cultivated under illumination of red and white lights. The growth rate under red light illumination
was almost the same as that in the basic conditions under white light illumination, but red light-grown cells accumulated
almost twice as much starch as white light-grown cells. Although there was a slight decrease in carbonic anhydrase activity,
red light-illuminated cells had almost 2.3 times the fructose-l,6-diphos-phatase activity of white light-illuminated cells.
Red light might stimulate starch accumulation by increasing the amounts of enzymes related to carbon fixation through the
phytochrome system. Cells grown under red light degraded 1.6 times as much starch and produced 1.7 times as much hydrogen
and 1.6 times as much ethanol compared with cells grown under white light during 12 h of dark anaerobic fermentation. 相似文献
77.
Glassy carbon electrodes modified with (5-amino-1,10-phenanthroline)bis(bipyridine)ruthium(II) chloride hydrate, [(bpy)2Ru(5-phenNH2)]Cl2·H2O, are shown to oxidize hydrazine with excellent sensitivity. The presence of an amine group on the ruthenium complex facilitates electropolymerization onto the electrode surface. Using cyclic voltammetry, a large catalytic current is observed upon oxidation of hydrazine in phosphate buffer (pH 5.0), compared to the current obtained from the ruthenium-modified electrode with no hydrazine present. The sensitivity of cyclic voltammetry is sufficient for obtaining a linear calibration curve for hydrazine over the range of 10−5 to 10−2 M. Hydrodynamic amperometry was used to determine the working potential for flow injection analysis. The limit of detection for hydrazine was determined to be 8.5 μM using FIA. The thickness of these films was shown to increase linearly with the number of electropolymerization cycles, in the range of 1000-2500 nm for 5-20 cycles, respectively, using Rutherford backscattering spectrometry (RBS). RBS analysis also suggests that the film is multilayered with the outermost layers containing a high ruthenium concentration, followed by layers where the concentration of ruthenium decreases linearly and approaches zero at the electrode surface. 相似文献
79.
Ewa Rudnik G. Matuschek N. Milanov A. Kettrup 《Journal of Thermal Analysis and Calorimetry》2006,85(2):279-284
Thermal behaviour of different starch derivatives, i.e. starch esters
and ethers having degree of substitution (DS) in the range of 0.02–0.18
were studied. Potato, maize and wheat starches were used. Measurements were
carried out by coupled thermal analysis/ mass spectrometry method (STA-MS)
in air atmosphere.
The major DTG peak during the investigation
for starch derivatives is observed below 300°C. The mass loss up to a
temperature of 300°C is about 50%. The most abundant ions found areH2O+
and CO2
+. For the studied
starch derivatives with a low degree of substitution (DS<0.18) no correlation
was found between thermal stability and the level of substitution regardless
of the nature of substitution. 相似文献
80.
Chemical conversion of various celluloses to glucose and its derivatives in supercritical water 总被引:16,自引:0,他引:16
The supercritical water biomass conversion system was designed and developed in our laboratory. The reaction vessel with cellulose sample was treated with this system at supercritical state of water for a designated period (3–105s) under the conditions of a tin bath temperature of 500°C and pressure of 35MPa. The recovered products of hydrolysates were then analyzed by high performance liquid chromatography. The obtained results indicated that a high amount of glucose and levoglucosan can be achieved from both celluloses I and II for 5–10s supercritical treatment, while that from starch for 3–5s treatment. Although this difference could be due to a difference in the molecular structure between cellulose and starch, a difference between celluloses I and II was not significant. Instead, an accessibility of the water towards cellulose molecules seemed to be significant for their chemical conversion. With the longer treatment, amounts of these compounds observed were decreased due to decomposition. Therefore, it may be concluded that, compared with acid hydrolysis or enzymatic saccharification, cellulose may be hydrolyzed to glucose and its derivatives more or less to the same degree as in corn starch under supercritical state. This finding suggests that the supercritical treatment can overcome the difficulties in hydrolyzing cellulose to glucose, found in the acid hydrolysis or enzymatic saccharification techniques. 相似文献