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81.
介绍了压缩天然气(CNG)加气站工艺技术,并着重分析了脱水、压缩、储气和安全等重点工序,还分别介绍了CNG加气子母站和CNG加气标准站平面布置图。在此基础上,根据不同CNG站的技术要求和本地区实际情况,选择CNG站建设方案。 相似文献
82.
Inter-domain routing data and Internet active probing measurements are two types of information commonly available in huge datasets and subject to extensive, focused analysis. However, the study of the correlation between these two complementary types of information still remains one of the most challenging problems in today’s research in networking. In this paper we describe a metaphor for the visualization of the interplay between the routing information exchanged via BGP and the round-trip delay measurements collected by several geolocated probes. We implemented a prototype based on the above metaphor. Our prototype highlights both the Autonomous System topology and the latency associated with each AS-path over time. Further, it shows how probes are partitioned into clusters associated with each border gateway, based on observed traffic patterns. The resulting visualization allows the user to explore the dynamics of the correlation between the two types of information. 相似文献
83.
84.
不饱和聚酯树脂光固化工艺的研究-光引发剂浓度 总被引:5,自引:2,他引:5
本文选用TPO、651两种光引发剂,分别配制引发剂浓度为0.25、0.5、1、2wt%的不饱和聚酯体系。通过测定光固化试样的显微硬度分析光引发剂浓度对固化程度的影响。结果表明,提高引发剂浓度能抑制氧阻聚的作用,但对于较厚的试样,引发剂浓度过高会导致固化不完全。 相似文献
85.
86.
Hai‐Xia Yang Yan‐Feng Li Jin‐Gang Liu Shi‐Yong Yang Da‐Xue Yin Lincheng Zhou Lin Fan 《应用聚合物科学杂志》2004,91(6):3981-3990
A series of new polymerized monomer reactants (PMR) matrix resins of poly(pyrrolone‐benzimidazole)s containing a pyridine unit (PPBP) were synthesized by polycondensation of monoethyl ester of cis‐5‐norbornene‐endo‐2,3‐dicarboxylic acid, 2,6‐diphenyl ester pyridinedicarboxylic acid or 3,5‐diphenyl ester pyridinedicarboxylic acid, and diethyl ester of 4,4′‐oxydiphthalic acid with 3,3′‐diaminobenzidine in a mixing solution of anhydrous ethyl alcohol and N‐methylpyrrolidone under given temperature and pressure conditions. The resulting resin solutions showed good solubility in polar organic solvents and stability at room temperature. The corresponding PPBP matrix resin, molded powder, and molded plate were prepared by undergoing amidation, imidization, cyclization, and crosslinking reactions when the reaction temperature was increased from 80 to 350°C, successively; the crosslinking structure was formed by the reverse Diels–Alder reaction at 270–290°C under 50 MPa pressure (2.5–3.5 MPa displayed by the pressure meter). The chemical reactions and properties of the resulting PPBP were studied by means of FTIR, TGA, and DMA methods, and the results indicated that the kinds of PPBP materials retain excellent thermal stability and processability; when the initial decomposition temperature was above 620°C the Tg was at 413.5°C for 3,5‐PPBP‐20 molded plate. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3981–3990, 2004 相似文献
87.
以丙烯酸-丙烯酰胺为单体,过硫酸钾为引发剂,N,N-亚甲基双丙烯酰胺为交联剂。水浴阶梯升温共聚合成耐盐性树脂,采用正交试验通过分析,研究了主要因素对产物性能的影响,确定较佳反应条件:T=50℃(2h)~65℃(3h),单体配比nAM:nAA=1:11,单体中和度[N]=90%~95%。引发剂浓度[I]=0.3%,单体浓度[M]=30%~35%,交联剂浓度[C]=0.025%~0.03%,并将此树脂作为缓释剂应用于固载二氧化氯中,取得了良好的效果。 相似文献
88.
以对氨基苯磺酸为起始原料 ,经过乙酰化、硝化、水解三步来制备标题物。通过正交试验找出了酰化的最佳反应条件为 :对氨基苯磺酸与乙酐的摩尔比为 1∶1.0 5 ,反应总时间为 1.5h ,反应温度为 2 5℃ ,酰化介质为酰化反应前用碳酸钠及水将对氨基苯磺酸完全溶解 ,使混合液 pH值为 5~ 6 ,反应过程中不再补加碳酸钠 ,其酰化转化率可达 99.6 % ,酰化产物的固体收率可达 96 .0 % ;硝化反应的最佳条件为 :硝化剂用 90 .2 %的硝酸 ,对乙酰氨基苯磺酸与硝化剂的摩尔比为 1∶1.0 5 ,反应温度为 10℃ ,浓硫酸与对乙酰氨基苯磺酸的摩尔比为 8.3∶1,其硝化转化率可达 96 .0 % ,硝化反应的选择性好 ,对氨基邻硝基苯磺酸的量不到 1.0 %。 相似文献
89.
Yun‐He Zhang Qin‐Hua Liu Ya‐Ming Niu Shu‐Ling Zhang Dong Wang Zhen‐Hua Jiang 《应用聚合物科学杂志》2005,97(4):1652-1658
A series of block copolymers composed of poly(ether ether ketone) (PEEK) and poly(ether ether ketone ketone) (PEEKK) components were prepared from their corresponding oligomers via a nucleophlilic aromatic substitution reaction. Various properties of the copolymers were investigated with differential scanning calorimetry (DSC) and a tensile testing machine. The results show that the copolymers exhibited no phase separation and that the relationship between the glass‐transition temperature (Tg) and the compositions of the copolymers approximately followed the formula Tg = Tg1X1 + Tg2X2, where Tg1 and Tg2 are the glass‐transition‐temperature values of PEEK and PEEKK, respectively, and X1 and X2 are the corresponding molar fractions of the PEEK and PEEKK segments in the copolymers, respectively. These copolymers showed good tensile properties. The crystallization kinetics of the copolymers were studied. The Avrami equation was used to describe the isothermal crystallization process. The nonisothermal crystallization was described by modified Avrami analysis by Jeziorny and by a combination of the Avrami and Ozawa equations. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1652–1658, 2005 相似文献
90.
Polycaproamide (PCA) and cationic dyeable poly(ethylene terephthalate) (CDP) polymers were blended mechanically (in ratios of 75/25, 50/50, and 25/75) in a melt twin‐screw extruder to prepare three PCA/CDP polyblended materials. The blends of PCA and CDP were spun into fibers. The molar ratio of dimethyl 5‐sulfoisophthalate sodium salt for CDP was 2%. This study investigated the physical properties of PCA/CDP polyblended fibers with nuclear magnetic resonance, gel permeation chromatography, gas chromatography, potentiometer, differential scanning calorimetry (DSC), thermogravimetric analysis, scanning electron microscopy (SEM), extension stress–strain measurements, density gradient analysis, and rheometry. The experimental results of DSC proved that PCA and CDP formed an immiscible system. In an SEM image of a 50/50 PCA/CDP blend, the morphological aggregation of a larger size, from 3 to 5 μm in diameter, was observed. The rheological behavior of the PCA/CDP polyblended materials exhibited negative‐deviation blends, and the 50/50 blend of the PCA/CDP polyblended fibers showed a minimum tenacity value. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1710–1715, 2004 相似文献