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51.
建筑结构粘结剂的研究进展   总被引:5,自引:1,他引:5  
在综合分析国内外文献的基础上,本文简述了粘结剂的发展历史,它在建筑业中的应用现状及在现代建筑业中的地位;研究了建筑结构粘结剂的主要性能指标,粘结剂连接的优点和主要技术检验指标等.此外,对目前广受关注的粘结剂耐久性研究的试验方法做了总结,列举了最新研究进展.在此基础上,指出了目前研究的不足,提出了对研究方向的建议.  相似文献   
52.
In the miniaturized designs of optical scanning systems, UV-curing adhesives have been substituted for screws and bolts. The assembly of delicate optical components enforces stringent requirements on positional accuracy and stability after temperature and humidity cycle testing. The influence of the UV-curing adhesive is mainly determined by its polymerization shrinkage (typically more than 6%). With low amounts of Aerosil® fillers (5% by weight), shrinkage values of 3% can be attained. Optimized adhesive constructions lead to close positional tolerances (0.5 μm) and angular displacements (0.1 mrad).  相似文献   
53.
A special unilateral NMR sensor has been designed for investigations of thin samples with a thickness of less than 1 mm and of surface effects of polymers. For use with the bar‐magnet NMR‐MOUSE®, the so‐called “crazy coil” is introduced with a low penetration depth. It is a flat meander coil etched on a printed circuit board with wiggles in the conductors. The design of the new coil and FEM simulations of the B 1 field are presented. Different applications are discussed by means of illustrative examples. They are the detection of surface damage in rubber samples, the swelling and drying of a latex membrane exposed to cyclohexane vapor mimicking a chemical sensor, and the drying of a thin sprayed adhesive layer.

Bar‐magnet NMR‐MOUSE® with crazy coil.  相似文献   

54.
复合薄膜用水性聚氨酯-丙烯酸酯胶粘剂的合成   总被引:3,自引:0,他引:3  
唐文静  傅和青  黄洪  陈焕钦 《精细化工》2007,24(10):1022-1025
以聚醚二元醇、甲苯二异氰酸酯(TDI)、二羟甲基丙酸(DMPA)等为原料合成了聚氨酯预聚体,用丙烯酸羟丙酯(HPA)将其部分封端,制得一种水性聚氨酯丙烯酸酯分散体,再加入乙烯基单体进行自由基引发聚合,制备出水性聚氨酯-丙烯酸酯(PUA)复合乳液。用红外光谱仪(FTIR)、差示量热扫描仪(DSC)、热重分析(TG)、马尔文粒度分析等测试手段,对合成产物进行了结构和性能表征。研究了软硬段质量比、亲水基团含量、丙烯酸酯单体的加入对PUA乳液性能的影响。结果表明,m(软段)∶m(硬段)=2∶1,m(PU)∶m(PA)=4∶1,—COOH质量分数为2.8%,以该乳液配制的胶粘剂应用于包装用CPP/CPP薄膜、OPP/VMOPP薄膜的剥离强度分别达31.9N/m和28.1 N/m。  相似文献   
55.
有机硅改性酚醛-丁腈胶粘剂的研究   总被引:2,自引:2,他引:2  
在酚醛 -丁腈胶粘剂中 ,加入一定量的有机硅材料 ,可有效提高其耐热性能 ,而其它性能基本不变。  相似文献   
56.
Seven different polymers used frequently as adhesives and/or matrix polymers in wood, wood composites, and natural fiber‐reinforced composites were studied by uniaxial tensile tests and nanoindentation. It was shown that the elastic modulus, the hardness, the creep factor, and the elastic‐, plastic‐, and viscoelastic work of indentation of the seven different polymers is essentially the same regardless whether the polymers were tested in the form of pure films or in situ, i.e., in an adhesive bond line with spruce wood. An excellent correlation was found between the elastic modulus measured by tensile tests and the elastic modulus measured by nanoindentation. In spite of the good correlation, the elastic modulus measured by nanoindentation is significantly higher than the elastic modulus measured by tensile tests. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:1234–1239, 2006  相似文献   
57.
The reaction of isocyanate in pressure sensitive adhesive (PSA) films adhered on to various adherends having different surface tensions was monitored by depth profiling using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy.In the latter stages of crosslinking reaction, unreacted isocyanate and its derivatives exist more in the bulk of the PSA than in the interfaces between PSA and adherends which are Teflon sheet and PE film having relatively lower surface tensions. In the case of using stainless steel having relatively higher surface tension as adherend, opposite segregation was observed compared to Teflon and PE.From X-ray photoelectron spectroscopy (XPS), it was revealed that N atoms exist more in surface than in bulk when stainless steel is used as adherend. We conclude that polyisocyanates migrate in the PSA film in order to minimize the magnitude of interfacial free energy between the PSA and the adherend, which leads to the change of surface tension of PSA film.  相似文献   
58.
Hot melts show many advantages over other adhesives, for instance, their lack of solvent and their very short setting time just by cooling. The weak point of hot melts in comparison to thermosetting resins is their limited thermal resistance. There is no doubt that the high performance hot melts on the basis of polyester and polyamide show a better heat performance than the widely-used rubbery hot melts. Nevertheless, it is true that the thermal resistance is limited by the melting point of the hot melt. To improve the heat performance, without losing the favourable hot melt properties, crosslinkable hot melts have been created. For the example, copolyamide/blocked isocyanate blends, it can be shown that crosslinkable hot melts are achievable in a wide range of reactivities. After curing, which takes place during the bonding process, these hot melts withstand temperatures of over 220°C even if the melting point of the initial hot melt was 100°C.  相似文献   
59.
Different materials have different coefficients of thermal expansion, which is a measure of the change in length for a given change in temperature. When different materials are combined structurally, as in a bonded joint, a temperature change leads to stresses being set up. These stresses are present even in an unloaded joint which has been cured at say 150°C and cooled to room temperature. Further stresses result from operations at even lower temperatures.

In addition to temperature-induced stresses, account also has to be taken of changes in adhesive properties. Low temperatures cause the adhesive to become more brittle (reduced strain to failure), while high temperatures cause the adhesive to become more ductile, but make it less strong and more liable to creep.

Theoretical predictions are made of the strength of a series of aluminium/CFRP joints using three different adhesives at 20°C and 55°C. Various failure criteria are used to show good correlation with experimental results.  相似文献   
60.
In order to improve the interfacial adhesion between aramid fiber (AF) and rubber matrix, a simple and facile method of aramid nanofiber (ANF) coating is demonstrated in this article. Tannic acid (TA) and polyethyleneimine (PEI) are polymerized in an alkaline solution to form a thin TA/PEI (TP) layer that is deposited on the surface of AF to introduce functional groups such as hydroxyl and amino groups. Then, the ANF coating is utilized to construct nanostructures on the surface of AF to improve the interfacial adhesion between the fiber and the rubber. Through hydrogen bonding and/or π-π stacking between the TP layer and the ANF, the ANF coating is firmly attached to the surface of AF. Compared with the untreated fiber, the interfacial adhesion of AF coated with ANF after 1, 3, 5, 7, 9 deposition cycles is increased by 27.8%, 29.1%, 31.5%, 43.1%, and 30.3%, and the mechanical properties of the fibers remain almost unchanged. This method shows its advantages of simple, facile, and time-effective, which is of great significance for industrial applications.  相似文献   
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