全文获取类型
收费全文 | 5487篇 |
免费 | 114篇 |
国内免费 | 21篇 |
学科分类
工业技术 | 5622篇 |
出版年
2023年 | 18篇 |
2022年 | 15篇 |
2021年 | 105篇 |
2020年 | 39篇 |
2019年 | 63篇 |
2018年 | 66篇 |
2017年 | 64篇 |
2016年 | 87篇 |
2015年 | 62篇 |
2014年 | 99篇 |
2013年 | 200篇 |
2012年 | 189篇 |
2011年 | 257篇 |
2010年 | 177篇 |
2009年 | 190篇 |
2008年 | 196篇 |
2007年 | 203篇 |
2006年 | 165篇 |
2005年 | 172篇 |
2004年 | 153篇 |
2003年 | 155篇 |
2002年 | 118篇 |
2001年 | 114篇 |
2000年 | 114篇 |
1999年 | 139篇 |
1998年 | 543篇 |
1997年 | 289篇 |
1996年 | 222篇 |
1995年 | 168篇 |
1994年 | 130篇 |
1993年 | 119篇 |
1992年 | 79篇 |
1991年 | 81篇 |
1990年 | 62篇 |
1989年 | 72篇 |
1988年 | 52篇 |
1987年 | 57篇 |
1986年 | 61篇 |
1985年 | 58篇 |
1984年 | 57篇 |
1983年 | 38篇 |
1982年 | 42篇 |
1981年 | 46篇 |
1980年 | 41篇 |
1979年 | 30篇 |
1978年 | 29篇 |
1977年 | 28篇 |
1976年 | 73篇 |
1975年 | 18篇 |
1974年 | 14篇 |
排序方式: 共有5622条查询结果,搜索用时 96 毫秒
121.
Abstract. The simultaneous switching autoregressive (SSAR) model proposed by Kunitomo and Sato (A non-linearity in economic time series and disequilibrium econometric models. In Theory and Application of Mathematical Statistics (ed. A. Takemura). Tokyo:University of Tokyo Press (in Japanese), 1994; Asymmetry in economic time series and simultaneous switching autoregressive model. Struct. Change Econ. Dyn. , forthcoming (1994).) is a Markovian non-linear time series model. We investigate the finite sample as well as the asymptotic properties of the least squares estimator and the maximum likelihood (ML) estimator. Due to a specific simultaneity involved in the SSAR model, the least squares estimator is badly biased. However, the ML estimator under the assumption of Gaussian disturbances gives reasonable estimates. 相似文献
122.
Masakazu Anpo Shinya Higashimoto Masaya Matsuoka Nurbosyn Zhanpeisov Yasushi Shioya Stanislaw Dzwigaj Michel Che 《Catalysis Today》2003,78(1-4):211-217
V-silicalite catalysts (VS-1 and VS-2) prepared by hydrothermal synthesis have been studied by ESR, XAFS (XANES and EXAFS) and photoluminescence spectroscopy. The in situ characterization of these V-silicalites shows that vanadium is present within the zeolitic framework as a highly dispersed tetrahedrally coordinated V-oxides, VO4 unit, having a short V=O bond length. Photoluminescence spectroscopy in static and dynamic mode, as well as XAFS studies allow to detect in the V-silicalites different V species than that present in V-HMS or V/SiO2, in terms of V=O bond length, vibrational energy,
bond angle and lifetime of the excited triplet state. It is suggested that the combined contribution of the neighboring Si---OH group attached to the VO4 unit and the zeolitic rigid framework structure of V-silicalites cause a more significant and pronounced effect on the chemical properties of the VO4 unit than the flexible structure of V-HMS or V/SiO2. Moreover, the dynamic quenching of the phosphorescence by the addition of reactant molecules such as NO or propane indicates that the V species in the excited triplet state can be expected to be the active sites for the photocatalytic reactions. 相似文献
123.
Continuous emulsion polymerizations of vinyl acetate were conducted at 50°C in a single continuous Couette–Taylor vortex flow reactor (CCTVFR) using sodium lauryl sulfate as emulsifier and potassium persulfate as initiator. The polymerization can be carried out very smoothly and stably, but the steady‐state monomer conversion attained in a CCTVFR is not as high as that in a plug flow reactor (PFR), but only slightly higher than that in a continuous stirred tank reactor (CSTR), even if the Taylor number is adjusted to an optimum value. Also, the effects of operating variables, such as the emulsifier, initiator, and monomer concentrations in the feed and the mean residence time on the kinetic behaviors were almost the same as those observed in a CSTR. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2755–2762, 2002 相似文献
124.
Kimiyasu Sato Miyuki Kawai Yuji Hotta Takaaki Nagaoka Koji Watari 《Journal of the American Ceramic Society》2007,90(4):1319-1322
Because the pyrolysis of organic substances can result in the emission of harmful pollutant gases, a reduction in the use of organic binders is one aim of today's ceramics industry. A novel ceramic-forming process was developed that requires considerably less organic binder than conventional techniques. The process involves immobilizing reactive molecules on the surfaces of the particles, which on subsequent irradiation with microwaves, form bridges that bind the entire particle assembly together. The chemical forces involved produce strong bonds, resulting in a significant reduction in the amount of organic binder that is required to maintain the shape of the ceramic green body. This method will help to decrease emissions of harmful gases produced from pyrolysis of the binder. 相似文献
125.
M. Takeuchi S. Ueno E. Flöter K. Sato 《Journal of the American Oil Chemists' Society》2002,79(7):627-632
The binary phase behavior of SOS (1,3-distearoyl-2-oleoyl-sn-glycerol) and SLS (1,3-distearoyl-2-linoleoyl-sn-glycerol) was examined by using DSC and conventional and synchrotron radiation X-ray diffraction. The solid-solution phases
were observed in the metastable α and γ forms in all concentration ranges. Results indicated that the miscible γ form did
not transform to the β′ form when the mixtures were subjected to simple cooling from a high-temperature liquid to a low-temperature
solid phase. However, and α-melt-mediated transformation into β′ and β2 resulted in the formation of immiscible phases in concentration ranges of SLS below 30%. By contrast, at SLS concentration
ranges above 30%, the α-melt-mediated transformation caused crystallization of only the γ form, and β′ and β2 crystals did not appear. These results show that the specific interactions between SOS and SLS are operative in the phase
behavior of the mixture states of SOS and SLS. 相似文献
126.
Masayuki Shirai Chandrashekhar V. Rode Eiichi Mine Akiyoshi Sasaki Osamu Sato Norihito Hiyoshi 《Catalysis Today》2006,115(1-4):248-253
Catalytic ring hydrogenations of naphthalene and 1-naphthol were studied over several supported metal catalysts in supercritical carbon dioxide solvent at low temperature. Higher concentration of hydrogen in supercritical carbon dioxide and lower reaction temperature were responsible for higher catalyst activity and selectivities to the desired partial ring hydrogenated products as compared with those observed in organic solvent for the same catalyst. 相似文献
127.
Koji Watari Hiromi Nakano Kimiyasu Sato Kazuyoshi Urabe Kozo Ishizaki Shixun Cao Katsunori Mori 《Journal of the American Ceramic Society》2003,86(10):1812-1814
The thermal conductivity of a SiC ceramic was measured as 270 W·m−1 ·K−1 at room temperature. At low temperatures ( T < 25 K), the decrease in the conductivity was proportional to T 3 on a logarithmic scale, which indicated that the conductivity was controlled by boundaries. The calculated phonon mean free path in the ceramic increased with decreased temperature, but was limited to ∼4 μm, a length almost equal to the grain size, at temperatures below 30 K. We concluded that the thermal conductivity of the ceramic below 30 K was influenced significantly by grain boundaries and grain junctions. 相似文献
128.
A -conjugated polymer, poly(pyridine-2,5-diyl) (PPy) was investigated as a support for CuCl2 in the synthesis of dimethyl carbonate by oxidative carbonylation of methanol. The PPy–CuCl2 adduct had high catalytic activity which was comparable to that of the homogeneous CuCl2 catalyst. The adduct caused corrosion of stainless-steel vessels only to minor extent, compared with the homogeneous CuCl2 catalyst. This PPy–CuCl2 catalyst was easily recycled by filtration and showed a similar catalytic activity in the third time use. The presence of the -conjugated system in PPy, through which electrons can move, may bring about the high catalytic activity for the oxidative carbonylation of methanol, which involves Cu(II)/Cu(I) redox processes. 相似文献
129.
Tsugio Sato Kenji Dosaka Toshiaki Yoshioka Akitsugu Okuwaki Kazuo Torii Yoshiro Onodera 《Journal of the American Ceramic Society》1992,75(3):552-556
Amorphous CeO2 –ZrO2 gels were prepared by coprecipitation in ammonia solutions. The onset of crystallization of the gels, from calcining in air, was 420°C, while 200° to 250°C in the presence of water and organic solvents such as methanol and ethanol. The sintering behaviors of CeO2 –ZrO2 powders were sensitive to the crystallizing conditions, since hard agglomerates formed when the precipitated gels were crystallized by normal calcination in air, whereas soft agglomerates formed when they were crystallized in water or organic solvents. CeO2 –ZrO2 powders crystallized in methanol and water at 250°C were sintered to full theoretical density at 1150° and 1400°C, respectively, whereas that crystallized by calcination in air at 450°C was sintered to only 95.2% of theoretical density, even at 1500°C. 相似文献
130.
The present study was carried out to examine if the positional distribution of medium-chain fatty acid (MCF) in dietary synthetic
fat influences lymphatic transport of dietary fat and the chemical composition of chylomicrons in rats with permanent cannulation
of thoracic duct. Four types of synthetic triacylglycerol were prepared: (i) sn-1(3) MCF-sn 2 linoleic acid, (ii) interesterified sn-1(3) MCF-sn 2 linoleic acid, (iii) sn-2 MCF-sn-1(3) linoleic acid, and (iv) interesterified sn-2 MCF-sn-1(3) linoleic acid. A purified diet composed of equal amounts of the synthetic fat and cocoa butter was given to rats with
permanent lymph duct cannulation. The positional distribution of MCF in the dietary fat had no significant effect on the lymph
flow, triacylglycerol output, phospholipid output, lipid composition of chylomicrons, or the particle size. The positional
distribution of MCF in the synthetic triacylglycerol was maintained in the chylomicron triacylglycerol. These results showed
that MCF in the dietary triacylglycerol is transported into lymphatics and the positional distribution is well preserved in
chylomicron triacylglycerol. 相似文献