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991.
新型环氧防腐涂料的研究   总被引:1,自引:0,他引:1  
蒋春莲 《辽宁化工》2005,34(2):68-70
采用在环氧树脂中加入纳米复合铁钛粉防锈颜料WD—D-325、固化剂、制备了新型环氧树脂防腐涂料。由于纳米技术的特性,该防腐涂料具有较高的防腐性、优异的附着力和柔韧性。实验确定了复合铁钛粉防锈颜料在环氧防腐涂料中的添加量。作为新型的环保颜料,复合铁钛粉防锈颜料可以替代红丹、锌铬黄等颜料。  相似文献   
992.
以(乙烯/乙酸乙烯酯/苯乙烯)三元共聚物(BS树脂)为增容荆,采用双螺杆挤出机制备了(丙烯腈/丁二烯/苯乙烯)共聚物(ABs)/镁盐晶须复合材料,研究了BS树脂、镁盐晶须用量对复合材料力学性能、流动性能的影响、结果表明,加入BS树脂有利于提高复合材料的拉伸强度和冲击强度,复合材料的熔体流动速率(MFR)随BS树脂用量增加而增大,且其MFR对温度或负荷呈非线性函数关系,比ABS对负荷更为敏感.  相似文献   
993.
Blends of polypropylene (PP) and thermoplastic elastomers (TPE), namely SBS (styrene‐butadiene‐styrene) and SEBS (styrene‐ethylene/1‐butene‐styrene) block copolymers, were prepared to evaluate the effectiveness of the TPE type as an impact modifier for PP and influence of the concentration of elastomer on the polymer properties. Polypropylene homopolymer (PP‐H) and ethylene–propylene random copolymer (PP‐R) were evaluated as the PP matrix. Results showed that TPEs had a nucleating effect that caused the PP crystallization temperature to increase, with SBS being more effective than SEBS. Microstructure characterization tests showed that in most cases PP/SEBS blends showed the smallest rubber droplets regardless of the matrix used. It was seen that SEBS is a more effective toughening agent for PP than SBS. At 0°C the Izod impact strength of the PP‐H/SEBS 30% b/w blend was twofold higher than the SBS strength, with the PP‐R/SEBS 30% b/w blend showing no break. A similar behavior on tensile properties and flexural modulus were observed in both PP/TPE blends. Yield stress and tensile strength decreased and elongation at break increased by expanding the dispersed elastomeric phase in the PP matrix. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 254–263, 2005  相似文献   
994.
The purpose of this work was to study how mineral fillers would behave in a polypropylene (PP) matrix when PP modified with maleic anhydride (MA) and/or itaconic acid (IA) was used as a coupling agent in the preparation of mineral‐filled PP composites. The composites were characterized with tensile mechanical measurements and morphological analysis. The optimum amount of the coupling agent to be used to obtain composites with improved mechanical properties was established. The results indicated that these coupling agents enhanced the tensile strength of the composites significantly, and the extent of the coupling effect depended on the nature of the interface that formed. The incorporation of coupling agents enhanced the resistance to deformation of the composite. The behavior of IA‐modified PP as a coupling agent was similar to that of a commercial MA‐modified PP for the filled PP composites. Evidence of improved interfacial bonding was revealed by scanning electron microscopy studies, which examined the surfaces of fractured tensile test specimens; their microstructures confirmed the mechanical results with respect to the observed homogeneous or optimized dispersion of the mineral‐filler phase in these composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2343–2350, 2007  相似文献   
995.
研究了各因素对纳米TiO2水悬浮液稳定性的影响,通过正交试验筛选出了最佳的分散工艺,解决了纳米TiO2在水性介质中的团聚问题.将分散后的纳米TiO2浆料加入到普通的水性苯丙乳液涂料中,加入各种助剂配制出了性能优异的水性纳米TiO2涂料,并对涂料的性能进行了测试.  相似文献   
996.
Although leather has a number of desirable properties such as thermal stability and fire retardancey, in addition to high toughness, it has a few drawbacks such as weight, high water absorption, poor soil and rot resistance, and nonuniformity. If these defects are overcome, leather's usefulness would be further enhanced and its competitive position with respect to synthetics would increase. This study reports the physical and mechanical properties of buffalo leather after chemical graft copolymerization with ethyl acrylate, butyl acrylate, and 2‐ethyl hexyl acrylate using benzoyl peroxide as an initiator. The optimum conditions for grafting (e.g., monomer and initiator concentrations, temperature and time of grafting, and solvent leather ratio) were extensively investigated. The study achieved outstanding properties for buffalo leather in reduction of water uptake after grafting, especially on using 2‐ethyl hexyl acrylate and butyl acrylate monomers. FT‐IR and solid 13C‐NMR for leather before and after grafting confirmed the grafting process.© 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1478–1483, 2003  相似文献   
997.
New thermosetting resins for applications of sheet‐molding compounds (SMCs) were successfully synthesized from linseed oil, which is the most molecularly unsaturated of all plant oils. The carbon–carbon double bonds were opened by epoxidation, followed by acrylation, and then maleinization, which provided more crosslink sites and added acid functionality on the triglyceride molecules to develop thickening. Dynamic mechanical analysis showed that the storage modulus of these new polymers was approximately 2.5 GPa at 30°C, and the glass‐transition temperature was above 100°C. During maturation the resins reached a molding viscosity quickly and stayed stable. Mechanical tests showed a flexural strength of 100 MPa and a flexural modulus of 2.8 GPa. Thermogravimetric analysis showed a single degradation ranging from 300°C–480°C, which was a result of the carbonization of the crosslinked network. These bio‐based resins are promising as replacements of some petroleum‐based resins in the SMC industry. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006  相似文献   
998.
Hann-Jang Hwang  Chun-Hung Li 《Polymer》2006,47(4):1291-1299
A novel bismaleimide (BMI), bis(4-maleimidophenoxy-3,5-dimethylphenyl)dicyclopentadiene (DCPDBMI), containing a large dicyclopentadiene (DCPD) and aryl ether linkage, was synthesized from bis(4-aminophenoxy-3,5-dimethylphenyl)dicyclopentadiene and maleic anhydride by the usual two-step procedure that included ring-opening addition to give bismaleamic acid, followed by cyclodehydration to bismaleimide. The monomers were characterized by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (NMR), elemental analyses (EA), and mass spectra (MS). A series of bismaleimide-triazine (BT) resins were prepared from synthesized bismaleimide (DCPDBMI) and then cured with 2,6-dimethyl phenol-dicyclopentadiene dicyanate ester (DCPDCY) at various molar ratios. Thermal properties of cured BT resins (DCPDBMI/DCPDCY) were studied using dielectric analyzer (DEA), dynamic mechanical analyzer (DMA) and thermalgravimetric analyzer (TGA). These data were compared with that of commercial bismaleimide (DDMBMI) cured with bisphenol A dicyanate ester (BADCY). The cured DCPDBMI/DCPDCY exhibits lower dielectric constant, dissipation factor and moisture absorption than those of DDMBMI/BADCY. The effects of blend composition on the glass transition temperatures and thermal stability are discussed.  相似文献   
999.
The three-way catalyst promoters (Ce-Zr)O2, (Pr-Ce-Zr)O2 and (Pr-Zr)O2 were prepared by the sol-gel method. The reduction/oxidation behavior of these mixed oxides was compared. It is shown that the formation of (Pr-Zr)O2 cubic solid solution at high temperature up to 800 °C makes it more reducible, and that the ternary solid solution that formed in (Pr-Ce-Zr)O2 mixed oxides plays an important role in the reduction process. The catalytic performance tests reveal that the introduction of a small amount of praseodymium into (Ce-Zr)O2 favors the light-off temperature of C3H6 and NO and the effectiveness for NO conversion at the lean region.  相似文献   
1000.
The self-sensing of stress by measurement of the relative dielectric constant (κ) has been shown in cement pastes containing steel fibers of 8 μm diameter and carbon filaments of 0.1 μm diameter. The κ value increases nonlinearly and quite reversibly with compressive stress up to 6.4 MPa, although the reversibility is not complete. Inferior sensing performance was observed in cement paste with carbon fibers of 15 μm diameter, although the performance was still better than cement paste without admixture.  相似文献   
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