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71.
Interpenetrating polymer networks (IPNs) of glycerol modified castor oil polyurethane (GC‐PU) and poly(2‐ethoxyethyl methacrylate) poly(2‐EOEMA) were synthesized using benzoyl peroxide as initiator and ethylene glycol dimethacrylate (EGDM) as crosslinker. GC‐PU/poly (2‐EOEMA) interpenetrating polymer networks were obtained by transfer molding. The novel GC‐PU/poly (2‐EOEMA) IPNs are found to be tough films. These IPNs are characterized in terms of their resistance to chemical reagents thermal behavior (DSC, TGA) and mechanical behavior, including tensile strength, Young's modulus, shore A hardness, and elongation. The morphological behavior was studied by scanning electron microscopy. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1029–1034, 2004 相似文献
72.
Poly(glycidyl methacrylate) (PGMA) beads with an average size of 350 μm were synthesized by suspension polymerization technique. The PGMA beads were first modified with iminodiacetonitrile (IDAN). Then, the IDAN‐modified beads were subsequently modified by hydroxylamine. The IDAN modification and the conversion of the nitrile groups to amidoxime were followed by FT‐IR spectroscopy. The surface morphology and thermal behavior of the PGMA and its modified forms were also characterized by scanning electron microscopy and thermogravimetric analysis techniques, further confirming modification and amidoximation. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
73.
Mirzaagha Babazadeh 《应用聚合物科学杂志》2006,102(5):4989-4995
A new polymerizable monomer, [4‐(9‐ethyl)carbazolyl]methyl methacrylate ( 2 ), was synthesized by reacting of methacrylic acid and 4‐hydroxymethyl‐9‐ethyl carbazole ( 1 ) by esterification procedure in the presence of N,N′‐dicyclohexylcarbodiimide. The resulting monomer was then polymerized free‐radically to form the poly(methyl methacrylate) containing 4‐(9‐ethyl)carbazolyl pend ent groups. Also, copolymerization of monomer 2 with various acrylic monomers such as methyl methacrylate, ethyl methacrylate, methyl acrylate, ethyl acrylate, and n‐butyl acrylate by azobisisobutyronitrile as a free radical polymerization initiator gave the related copolymers in high yields. The structure of all the resulted compounds was characterized and confirmed by FTIR and 1H NMR spectroscopic techniques. The average molecular weight of the obtained polymers was determined by gel permeation chromatography using tetrahydrofurane as the solvent. The thermal gravimetric analysis and differential scanning calorimeter instruments were used for studying of thermal properties of polymers. It was found that, with the incorporation of bulky 4‐(9‐ethyl)carbazolyl substitutes in side chains of methyl methacrylate polymers, thermal stability and glass transition temperature of polymers are increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4989–4995, 2006 相似文献
74.
75.
Viscosimetric measurements were obtained with the ternary systems polystyrene/dioxane/methanol, polystyrene/benzene/methanol and poly(methyl methacrylate)/dioxane/cyclohexane, changing the solvent mixture composition at constant temperature. The polystyrene and poly(methyl methacrylate) systems exhibit a transition phenomenon with solvent-mixture composition in which the polymer is just above the theta condition. In the case where two theta conditions occur ((θ-intra, θ-inter) the transition point is closely related to the intramolecular theta conditions. Moreover the intramolecular theta conditions vary with the molecular weight in the region of molecular weights where the preferential adsorption also varies. This variation induces a variation of the transition point with molecular weight which obeys a formula analogous to that giving the variation of the preferential adsorption with molecular weight. 相似文献
76.
Acrylate and methacrylate monomers were obtained by reacting vernonia oil, a naturally epoxidized oil, with acrylic or methacrylic acid. The highest conversion (85–98%) of epoxy groups was obtained when the reaction was performed with an excess of the carboxylic acid at 100–120°C. The acrylate and methacrylate monomers of vernonia oil were characterized by IR and NMR spectroscopy. These monomers were then cured by sunlight in the presence of benzophenone to produce transparent films. In addition, interpenetrating polymer neworks (IPNs) were prepared in a two‐step technique from the sunlight‐cured methacrylate of vernonia oil, as the elastomeric component, in combination with a cured epoxy resin (a bisphenol A–type resin). Dynamic mechanical analysis showed good compatibility between the networks of the two cured polymers. An IPN with a 1 : 1 composition of the two polymer components exhibited the properties of a reinforced elastomer. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3835–3843, 2004 相似文献
77.
用共沉淀法制备Fe3O4磁流体,总结出用十二烷基磺酸钠与聚乙二醇作为表面活性剂制备水基磁流体的合适条件:(1)反应温度为室温或不高于35℃;(2)表面活性剂十二烷基磺酸钠的最佳用量为0.0030~0.0040 g/80 mL;(3)第一次包裹的最佳pH为9~10;(4)聚乙二醇作为第二次包裹的表面活剂时,体系最佳温度为40℃左右;(5)表面活性剂聚乙二醇的最佳用量为0.0050~0.0060 g/80 mL。通过实验制得了能稳定存在180 d的水基磁流体。并用透射电镜、红外光谱、分光光度计、古埃磁天平等进行了初步表征。 相似文献
78.
选用两种不同牌号的ABS树脂与PMMA共混,对其组成与性能的关系进行了详细的研究。试验结果表明,不同组成的ABS对ABS/PMMA混合物的光学性能、力学性能以及流变行为的影响都有显著的不同. 相似文献
79.
高吸水性树脂与PVC共混的研究 总被引:5,自引:0,他引:5
用高吸水性树脂与PVC共混制备了吸水膨胀性PVC共混物。实验证明,部分水解丙烯酸甲酯—醋酸乙烯酯HP(MA—VAC)和丙烯酸甲酯—醋酸乙烯酯—甲基丙烯酸甲酯HP(MA—VAC—MMA)共聚物与PVC共混效果更好。研究了影响共混物吸水率和力学性质的各种因素。结果表明,随高吸水性树脂用量增加,共混物吸水率显著增加。当吸水树脂用量大于40%时,共混物的拉伸强度和断裂仲长率下降。共混物最大吸水率达22.17克水/克共混物,最大膨胀度为15倍。 相似文献
80.
Homogenous polymerization of methyl methacrylate using Pd(II)- and Ni(II)-based acetylide complexes as initiators has been investigated. M(PR'3)2(CCR)2 (M=Pd, Ni; R'=PPh3, Pn-Bu3; R=Ph, CH2OH, CH2OOCCH3, CH2OOCPh, CH2OOCPhOH-o) were found to be a novel type of effective initiators for the polymerization of methyl methacrylate. Among them, Pd(C CPh)2(PPh3)2 (PPP) shows the highest activity in the MMA polymerization and the PMMA obtained is a syndiotactic polymer with high number-average molecular weight (M
n) of 14.1 × 104. Some features and kinetic behavior of MMA polymerization initiated by PPP were studied in detail. The polymerization reaction is first-order with respect to both [PPP] and [MMA]. Radical polymerization mechanism is proposed. 相似文献