全文获取类型
收费全文 | 10300篇 |
免费 | 568篇 |
国内免费 | 5篇 |
专业分类
电工技术 | 153篇 |
综合类 | 9篇 |
化学工业 | 3061篇 |
金属工艺 | 119篇 |
机械仪表 | 190篇 |
建筑科学 | 324篇 |
矿业工程 | 14篇 |
能源动力 | 277篇 |
轻工业 | 2443篇 |
水利工程 | 67篇 |
石油天然气 | 51篇 |
无线电 | 649篇 |
一般工业技术 | 1288篇 |
冶金工业 | 1250篇 |
原子能技术 | 52篇 |
自动化技术 | 926篇 |
出版年
2024年 | 22篇 |
2023年 | 133篇 |
2022年 | 477篇 |
2021年 | 553篇 |
2020年 | 281篇 |
2019年 | 310篇 |
2018年 | 326篇 |
2017年 | 330篇 |
2016年 | 365篇 |
2015年 | 274篇 |
2014年 | 451篇 |
2013年 | 675篇 |
2012年 | 624篇 |
2011年 | 674篇 |
2010年 | 503篇 |
2009年 | 492篇 |
2008年 | 469篇 |
2007年 | 431篇 |
2006年 | 311篇 |
2005年 | 270篇 |
2004年 | 222篇 |
2003年 | 203篇 |
2002年 | 175篇 |
2001年 | 125篇 |
2000年 | 137篇 |
1999年 | 140篇 |
1998年 | 417篇 |
1997年 | 243篇 |
1996年 | 174篇 |
1995年 | 117篇 |
1994年 | 119篇 |
1993年 | 102篇 |
1992年 | 56篇 |
1991年 | 45篇 |
1990年 | 39篇 |
1989年 | 69篇 |
1988年 | 41篇 |
1987年 | 42篇 |
1986年 | 46篇 |
1985年 | 38篇 |
1984年 | 36篇 |
1983年 | 34篇 |
1982年 | 29篇 |
1981年 | 31篇 |
1980年 | 26篇 |
1979年 | 26篇 |
1978年 | 30篇 |
1977年 | 34篇 |
1976年 | 48篇 |
1974年 | 14篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
81.
In this work, the effect of the introduction of modified solid surfaces into polymer blends on the phase‐separation process was investigated. Glass fibers with surfaces having different chemistries were introduced into polystyrene–poly(methyl methacrylate) blends. The glass fibers used either had fully hydrated surfaces or had surfaces covered with a random copolymer, poly(styrene‐co‐methyl methacrylate). The copolymer was synthesized by free‐radical polymerization of styrene and methyl methacrylate in the presence of previously vinyl silane‐treated glass fibers. The copolymerization and grafting procedures were investigated by FTIR and thermal analysis. Blends containing the fibers were studied using FTIR microscopy and optical microscopy. FTIR microscopy results showed that the composition of the phases in the blends was shifted by using fibers with different surface chemistries. Fibers with grafted copolymers were capable of narrowing the immiscibility region in the phase diagram, while fully hydrated fibers were able to expand the gap. It was proposed that interfacial interactions regulated by a hydrophilic–hydrophobic type of forces were responsible for guiding the described phase‐separation process. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1619–1627, 2003 相似文献
82.
Ana Paula Vieira Soares Manuel Farinha Portela Alain Kiennemann 《Catalysis Reviews》2005,47(1):125-174
This review deals with the important industrial reaction of formaldehyde manufacture by methanol oxidation over iron molybdate catalysts. Detailed reference is made to the used catalyst, preparation techniques (coprecipitation, sol-gel like, mechanical mixing, etc.) including unsupported and supported catalysts, promoters and characterization methods. The controversial active phase assignment (stoichiometric versus Mo rich iron molybdate) is discussed. The proposed reaction mechanisms and kinetic laws for the main and side reactions are examined. The catalyst deactivation processes are reviewed and the role of Mo excess on these processes is underlined. Finally conclusions and perspectives are presented. 相似文献
83.
André Lourenço Hugo Plácido da Silva Carlos Carreiras Ana Priscila Alves Ana L. N. Fred 《Multimedia Tools and Applications》2014,70(1):433-460
With the advent of wearable sensing and mobile technologies, biosignals have seen an increasingly growing number of application areas, leading to the collection of large volumes of data. One of the difficulties in dealing with these data sets, and in the development of automated machine learning systems which use them as input, is the lack of reliable ground truth information. In this paper we present a new web-based platform for visualization, retrieval and annotation of biosignals by non-technical users, aimed at improving the process of ground truth collection for biomedical applications. Moreover, a novel extendable and scalable data representation model and persistency framework is presented. The results of the experimental evaluation with possible users has further confirmed the potential of the presented framework. 相似文献
84.
Shigenobu Kobayashi Tomiji Wakida Shouhua Niu Satoshi Hazama Taisuke Ito Yoshiyuki Sasaki 《Coloration Technology》1995,111(3):72-76
Three kinds of aramid fabrics, Technora (modified p-aramid), Conex (m-aramid) and Kevlar (p-aramid), were subjected to sputter etching and argon low-temperature plasma treatments after dyeing in black with disperse dyes. The depth of shade increased considerably on Technora and Kevlar with the sputter etching treatment, but not on Conex fabrics. Argon low-temperature plasma treatment had virtually no effect on the depth of shade on the aramid fabrics. 相似文献
85.
Andres T Aguayo Ana G Gayubo Ana M Tarrío Alaitz Atutxa Javier Bilbao 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2002,77(2):211-216
With the aim of determining the possibilities of directly upgrading the liquid obtained from carbohydrate fermentation, the effect of operating conditions (temperature, space time, water content in the feed) has been studied in the catalytic transformation of aqueous ethanol into hydrocarbons on an HZSM‐5 zeolite in an isothermal fixed bed reactor. Special attention has been paid to the effect of water content on the yield, product distribution and catalyst deactivation. Although deactivation by coke decreases as the water content is increased, this content must be limited at 450 °C and higher temperatures in order to avoid irreversible deactivation of the catalyst by dealumination. © 2002 Society of Chemical Industry 相似文献
86.
Abstract. Several models have been proposed in recent years for analysing spatial data and also, to some extent, spatio‐temporal data. One of the important problems, namely the choice of an appropriate model for describing real data sets, remains unsolved. Here we consider the analysis of spatio‐temporal processes from which observations over space and time are available. We propose statistical tests for discriminating between space–time autoregressive processes and multivariate autoregressive processes. The sampling properties of the proposed tests are considered. We illustrate the methods with a real example. We use the above tests to find the best model to describe spatio‐temporal variations of hourly carbon monoxide measurements at four locations in London in January 2004. 相似文献
87.
Liver nuclear incorporation of stearic (18∶0), linoleic (18∶2n−6), and arachidonic (20∶4n−6) acids was studied by incubation
in vitro of the [1-14C] fatty acids with nuclei, with or without the cytosol fraction at different times. The [1-14C] fatty acids were incorporated into the nuclei as free fatty acids in the following order: 18∶0>20∶4n−6≫18∶2n−6, and esterified
into nuclear lipids by an acyl-CoA pathway. All [1-14C] fatty acids were esterified mainly to phospholipids and triacylglycerols and in a minor proportion to diacylglycerols.
Only [1-14C] 18∶2n−6-CoA was incorporated into cholesterol esters. The incorporation was not modified by cytosol addition. The incorporation
of 20∶4n−6 into nuclear phosphatidylcholine (PC) pools was also studied by incubation of liver nuclei in vitro with [1-14C]20∶4n−6-CoA, and nuclear labeled PC molecular species were determined. From the 15 PC nuclear molecular species determined,
five were labeled with [1-14C]20∶4n−6-CoA: 18∶0–20∶4, 16∶0–20∶4, 18∶1–20∶4, 18∶2–20∶4, and 20∶4–20∶4. The highest specific radioactivity was found in
20∶4–20∶4 PC, which is a minor species. In conclusion, liver cell nuclei possess the necessary enzymes to incorporate exogenous
saturated and unsaturated fatty acids into lipids by an acyl-CoA pathway, showing specificity for each fatty acid. Liver cell
nuclei also utilize exogenous 20∶4n−6-CoA to synthesize the major molecular species of PC with 20∶4n−6 at the sn-2 position. However, the most actively synthesized is 20∶4–20∶4 PC, which is a quantitatively minor component. The labeling
pattern of 20∶4–20∶4 PC would indicate that this molecular species is synthesized mainly by the de novo pathway. 相似文献
88.
Paula Relgio Marie-Thrse Charreyre Jos Paulo S. Farinha Jos M.G. Martinho Christian Pichot 《Polymer》2004,45(26):8639-8649
N,N-dimethylacrylamide (DMA) and N-acryloxysuccinimide (NAS) were copolymerized by the reversible addition–fragmentation chain transfer (RAFT) polymerization technique, to obtain random and block copolymer precursors onto which different side-groups may be statistically grafted via the reactive NAS units. These reactive copolymers have interesting applications in various fields such as coatings and paints, water purification and biology. Random poly(DMA-co-NAS) copolymer chains were synthesized with a 75/25 molar ratio, high conversion, an excellent molecular weight (MW) control from 5000 to 130 000 g mol−1, and low polydispersity index (Mw/Mn<1.1). Poly(DMA-b-NAS) block copolymers were synthesized by a two step method, in which a poly(DMA) homopolymer was prepared first and then used as macro-chain transfer agent to polymerize NAS. For example, a poly(DMA-b-NAS) sample was obtained with an average molecular weight of 44 300/7400 g mol−1 corresponding to 447 DMA and 44 NAS units. Such block copolymers had not yet been synthesized by any controlled polymerization technique. They can be used to prepare polymers with exactly the same backbone and an increasing number of different side groups (e.g. hydrophobic, ionic or fluorescent). 相似文献
89.
Masanori Hirano Keisuke Ota Takaharu Ito 《Journal of the American Ceramic Society》2005,88(12):3303-3310
Anatase-type TiO2 powder containing sulfur with absorption in the visible region was directly formed as particles with crystallite in the range 15–88 nm by thermal hydrolysis of titanium(III) sulfate (Ti2 (SO4 )3 ) solution at 100°–240°C. Because of the presence of ammonium peroxodisulfate ((NH4 )2 S2 O8 ), the yield of anatase-type TiO2 from Ti2 (SO4 )3 solution was accelerated, and anatase with fine crystallite was formed. Anatase-type TiO2 doped with ZrO2 up to 9.8 mol% was directly precipitated as nanometer-sized particles from the acidic precursor solutions of Ti2 (SO4 )3 and zirconium sulfate in the presence and the absence of (NH4 )2 S2 O8 by simultaneous hydrolysis under hydrothermal conditions at 200°C. By doping ZrO2 into TiO2 and with increasing ZrO2 content, the crystallite size of anatase was decreased, and the anatase-to-rutile phase transformation was retarded as much as 200°C. The anatase-type structure of ZrO2 -doped TiO2 was maintained after heating at 1000°C for 1 h. The favorable effect of doping ZrO2 to anatase-type TiO2 on the photocatalytic activity was observed. 相似文献
90.