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771.
In this work, polypropylene (PP)/octene-ethylene copolymer (POE) blends were injection-molded using the so- called dynamic packing injection technique, which imposed oscillatory shear on the gradually cooling melt during the packing solidification stage. In this way, the effect of shear on the size distribution and anisotropy of the minor phase droplets could be investigated. Besides, by using two kinds of POE with different octene contents, the effect of component miscibility was also studied. The results show that the droplet size is mainly determined by composition and miscibility, and droplet anisotropy is mainly determined by droplet size and shear. Most importantly, under the same processing condition, droplet anisotropy increases with droplet size, and there seems a linear fit between them, disregarding the miscibility factor. These results may provide guidance for preparing polymer blends with desired properties by tailoring their phase morphologies. 相似文献
772.
Matrix/fiber composites of β-form isotactic polypropylene(iPP) matrix and α-iPP or PA6 fibers were prepared by laminating technique under different preparation temperatures. The mechanical properties and interfacial morphologies of these composites were studied by tensile test, optical microscopy and scanning electron microscopy, respectively. The experimental results show that the tensile yield load and tensile modulus of β-iPP/PA6 matrix/fiber systems increased significantly at the expense of elongation at break. These mechanical properties show essentially no dependence on the sample preparation temperature. On the other hand, the mechanical properties of iPP matrix/fiber single polymer composites depend strongly on the sample preparation temperature. At low sample preparation temperature, e.g., 172 ℃, the solid α-iPP fiber induces α-iPP crystallization, leading to the formation of α-iPP transcrystalline layer around the fiber. This results in a remarkable increment of the tensile yield load and tensile modulus. The elongation at break is also much better than that of the iPP/PA6 matrix/fiber system. It reflects a better interfacial adhesion of the single polymer composite compared with the iPP/PA6 composite. At higher sample preparation temperature, e.g., 174 ℃ or 176 ℃, the partial surface melting of the oriented fiber allows interdiffusion of iPP molecular chains in the molten fiber and matrix melt. The penetration of matrix chains into the molten iPP fiber results in some iPP molecular chains being included partially in the recrystallized fiber and the induced β-transcrystalline layers. This kind of configuration leads to an improvement of interfacial adhesion between the fiber and matrix, which causes a simultaneous increase of the tensile yield load, tensile modulus and elongation at break of β-iPP. 相似文献
773.
采用熔融共混法制备可生物降解聚碳酸亚丙酯(PPC)/相容剂/聚丙烯(PP)纺粘非织造布切片,分别研究相容剂马来酸酐(MAH)、马来酸酐接枝聚丙烯(PP-2)、马来酸酐-苯乙烯接枝聚丙烯(PP-g-(MAH-coSt))对切片性能的影响.当mPPC∶mPP为70∶30时,相容剂MAH、PP-2、PP-g-(MAH-co-St)的最优用量分别为PPC和PP总质量的1%、3%、8%,在最优用量下PPC/相容剂/PP纺粘非织造布切片的拉伸强度分别为20.16、21.27、26.34 MPa,熔体流动速率(MFR)分别为81.6 g/10min、103.6 g/10min、46.4 g/10min,T-5%较不添加相容剂时提高了50.5、10.0、28.0 K,扫描电镜图显示加了相容剂的切片内部结构紧密,相容性较好,30天降解率在3.12%以上.红外和核磁谱图表明相容剂PP-g-(MAH-co-St)的作用机理是其酸酐基团和PPC发生了开环反应,通过化学键作用促进PPC与PP相容.相容剂改善了切片的力学性能、热学性能和降解性能,提高了切片的界面粘附力和相容性,在满足纺粘生产工艺下,切片的综合性能和加工温度范围得到提高,为制备具有良好综合性能的可生物降解纺粘非织造布切片提供了理论数据. 相似文献
774.
Ya-Nan Ye Pei-Yuan Li Yong-Gang Shangguan Zhi-Sheng Fu Qiang Zheng Zhi-Qiang Fan 《中国化学快报》2014,25(4):596-600
Both terminated functional isotactic polypropylene (iPP) and block copolymers containing iPP segment are desirable for commercial applications. This paper provides a convenient, highly-efficient method to prepare hydroxyl-terminated isotactic polypropylene (iPP-t-OH) and functional di-block copolymer containing the iPP segment through a combination of coordination polymerization and coupling reaction. The coordination polymerization was catalyzed by TiCI4/MgCI2/AIEt3 catalyst system using ZnEt2 as chain transfer agent. Further, the Zn-terminated iPP was oxidized and subsequently hydrolyzed to provide iPP-t-OH. Soxhlet extraction and 13C NMR were used to calculate the isotacticity of iPP-t-OH. The degree of polymerization and the number of hydroxyl groups at the chain end of iPP-t-OH were measured by GPC and 1H NMR. Despite the high molecular weight and heterogeneous reaction, iPP-t-OH is effectively linked with PEG-t-NCO to produce di-block copolymers. DSC analysis of the di-block copolymer shows an obvious decrease in Tm and To, which indicated that PEG was successfully linked to the terminal end of iPP. 相似文献
775.
In an effort to reduce thermal shrinkage and improve electrochemical performance of porous polypropylene (PP) separators for lithium-ion batteries, a new composite separator is developed by introducing ceramic coated layers on both sides of PP separator through a dip-coating process. The coated layers are comprised of heat-resistant and hydrophilic silica nanoparticles and polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) binders. Highly porous honeycomb structure is formed and the thickness of the layer is only about 700 nm. In comparison to the pristine PP separator, the composite separator shows significant reduction in thermal shrinkage and improvement in liquid electrolyte uptake and ionic conduction, which play an important role in improving cell performance such as discharge capacity, C-rate capability, cycle performance and coulombic efficiency. 相似文献
776.
通过在反应器间加入不同的外给电子体,控制Ziegler-Natta催化剂催化丙烯聚合反应,并对聚丙烯立构规整度分布、超高分子量聚丙烯组分以及共聚单体分布情况进行了研究,结果表明,应用此方法可获得立构规整性分布受控、超高分子量组分含量高以及橡胶相增韧效果好的聚丙烯树脂. 相似文献
777.
778.
聚并苯纳米颗粒与聚丙烯复合制备新型抗静电阻燃材料 总被引:2,自引:0,他引:2
用聚并苯纳米颗粒作为新型导电填料代替导电炭黑和石墨等, 制备出具有抗静电阻燃性能的纳米聚并苯/聚丙烯复合材料. 测定了复合材料的渗流转变区, 讨论了纳米聚并苯含量对复合材料体积电阻率和表面电阻率的影响. 实验结果表明, 所制备复合材料的渗流转变发生在纳米聚并苯质量分数为16.7%-28.6%范围内, 当纳米聚并苯含量为28.6%时, 体积电阻率下降至2.09×107 Ω·cm. 另外, 阻燃性能研究结果表明, 当纳米聚并苯质量分数为23.1%时, 复合材料在空气中可以自熄, 因而可应用于矿井中抗静电阻燃塑料管道. 相似文献
779.
780.