全文获取类型
收费全文 | 1336篇 |
免费 | 122篇 |
国内免费 | 225篇 |
专业分类
化学 | 1377篇 |
晶体学 | 26篇 |
力学 | 3篇 |
综合类 | 9篇 |
数学 | 2篇 |
物理学 | 266篇 |
出版年
2024年 | 2篇 |
2023年 | 13篇 |
2022年 | 23篇 |
2021年 | 26篇 |
2020年 | 35篇 |
2019年 | 46篇 |
2018年 | 40篇 |
2017年 | 48篇 |
2016年 | 64篇 |
2015年 | 49篇 |
2014年 | 78篇 |
2013年 | 123篇 |
2012年 | 71篇 |
2011年 | 75篇 |
2010年 | 80篇 |
2009年 | 68篇 |
2008年 | 75篇 |
2007年 | 89篇 |
2006年 | 67篇 |
2005年 | 74篇 |
2004年 | 80篇 |
2003年 | 50篇 |
2002年 | 54篇 |
2001年 | 42篇 |
2000年 | 29篇 |
1999年 | 34篇 |
1998年 | 40篇 |
1997年 | 18篇 |
1996年 | 22篇 |
1995年 | 30篇 |
1994年 | 37篇 |
1993年 | 23篇 |
1992年 | 14篇 |
1991年 | 11篇 |
1990年 | 8篇 |
1989年 | 6篇 |
1988年 | 6篇 |
1987年 | 7篇 |
1985年 | 3篇 |
1984年 | 4篇 |
1983年 | 4篇 |
1982年 | 5篇 |
1981年 | 3篇 |
1980年 | 1篇 |
1979年 | 4篇 |
1975年 | 1篇 |
1969年 | 1篇 |
排序方式: 共有1683条查询结果,搜索用时 15 毫秒
11.
Infrared and nuclear magnetic resonance (NMR) spectroscopies have been applied for quantitative comparison on unsaturated bonds in tetrafluoroethylene (TFE)-propylene (P)-vinylidene fluoride (VdF) terpolymers. These spectroscopies have led to consistent results while they are based on completely different principles. It is shown that the absolute concentration can be evaluated from NMR measurements. The behavior of unsaturation has been discussed in terms of after-treatment such as wet and dry treatments. The result obtained here can give the important information to improve the performance of fluoroelastomer based on TFE-P-VdF terpolymers. 相似文献
12.
13.
R. Souzy B. Ameduri B. Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2004,42(20):5077-5097
The radical co‐ and terpolymerization of 4‐[(α,β,β‐trifluorovinyl)oxy]bromo benzene (TFVOBB) with 1,1‐difluoroethylene (or vinylidene fluoride, VDF, or VF2), hexafluoropropene (HFP), perfluoromethyl vinyl ether (PMVE), and chlorotrifluroroethylene (CTFE) is presented. Although TFVOBB could be thermocyclodimerized, it could not homopolymerize under radical initiation. TFVOBB could be copolymerized in solution under a radical initiator with VDF or CTFE comonomers, while its copolymerization with HFP or PMVE were unsuccessful. The terpolymerization of TFVOBB with VDF and HFP, or VDF and PMVE, or VDF and CTFE also led to original fluorinated terpolymers bearing bromoaromatic side‐groups. The conditions of co‐ and terpolymerization were optimized in terms of the nature of the radical initiators, and of the nature of solvents (fluorinated or nonhalogenated). Various monomer concentrations in the co‐ and terpolymers were assessed by 19F and 1H‐NMR spectroscopy. The thermal and physico chemical properties were also studied. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5077–5097, 2004 相似文献
14.
L. Sauguet B. Ameduri B. Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2006,44(15):4566-4578
The radical terpolymerization of 8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene with vinylidene fluoride (VDF) and perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride is presented. Changing the feed compositions of these three fluorinated comonomers enabled us to obtain different random‐type poly[vinylidene fluoride‐ter‐perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride‐ter‐8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene] terpolymers containing various sulfonyl fluoride and brominated side groups. Yields higher than 70% were reached in all cases. The hydrolysis of the sulfonyl fluoride group into the ? SO3Li function in the presence of lithium carbonate was quantitatively achieved without the content of VDF being affected, and so dehydrofluorination of the VDF base unit was avoided. These original terpolymers were then crosslinked via dangling bromine atoms in the presence of a peroxide/triallyl isocyanurate system, which produced films insoluble in organic solvents such as acetone and dimethylformamide (which totally dissolved uncured terpolymers). The acidification of ? SO3Li into the ? SO3H function enabled protonic membranes to be obtained. The thermal stabilities of the crosslinked materials were higher than those of the uncured terpolymers, and their electrochemical performances were investigated. According to the contents of the sulfonic acid side functions, the ion‐exchange capacities ranged from 0.6 to 1.5 mequiv of H+/g, whereas the water uptake and conductivities ranged from 5–26% (±11%) and from 0.5 to 6.0 mS/cm, respectively. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4566–4578, 2006 相似文献
15.
Yiwang Chen Dongmei Liu Qilan Deng Xiaohui He Xiaofeng Wang 《Journal of polymer science. Part A, Polymer chemistry》2006,44(11):3434-3443
The direct preparation of grafting polymer brushes from commercial poly (vinylidene fluoride) (PVDF) films with surface‐initiated atom transfer radical polymerization (ATRP) is demonstrated. The direct initiation of the secondary fluorinated site of PVDF facilitated grafting of the hydrophilic monomers from the PVDF surface. Homopolymer brushes of 2‐(N,N‐dimethylamino)ethyl methacrylate (DMAEMA) and poly (ethylene glycol) monomethacrylate (PEGMA) were prepared by ATRP from the PVDF surface. The chemical composition and surface topography of the graft‐functionalized PVDF surfaces were characterized by X‐ray photoelectron spectroscopy, attenuated total reflectance/Fourier transform infrared spectroscopy, and atomic force microscopy. A kinetic study revealed a linear increase in the graft concentration of poly[2‐(N,N‐dimethylamino)ethyl methacrylate] (PDMAEMA) and poly[poly(ethylene glycol) monomethacrylate] (PPEGMA) with the reaction time, indicating that the chain growth from the surface was consistent with a controlled or living process. The living chain ends were used as macroinitiators for the synthesis of diblock copolymer brushes. The water contact angles on PVDF films were reduced by the surface grafting of DMAEMA and PEGMA. Protein adsorption experiments revealed a substantial antifouling property of PPEGMA‐grafted PVDF films and PDMAEMA‐grafted PVDF films in comparison with the pristine PVDF surface. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3434–3443, 2006 相似文献
16.
Tim R. Dargaville Julie M. Elliott Mathew Celina 《Journal of Polymer Science.Polymer Physics》2006,44(22):3253-3264
Films of piezoelectric PVDF and P(VDF‐TrFE) were exposed to vacuum UV (115–300 nm VUV) and γ‐radiation to investigate how these two forms of radiation affect the chemical, morphological, and piezoelectric properties of the polymers. The extent of crosslinking was almost identical in both polymers after γ‐irradiation, but surprisingly, was significantly higher for the TrFE copolymer after VUV‐irradiation. Changes in the melting behavior were also more significant in the TrFE copolymer after VUV‐irradiation due to both surface and bulk crosslinking, compared with only surface crosslinking for the PVDF films. The piezoelectric properties (measured using d33 piezoelectric coefficients and D‐E hysteresis loops) were unchanged in the PVDF homopolymer, while the TrFE copolymer exhibited more narrow D‐E loops after exposure to either γ‐ or VUV‐radiation. The more severe damage to the TrFE copolymer in comparison with the PVDF homopolymer after VUV‐irradiation is explained by different energy deposition characteristics. The short wavelength, highly energetic photons are undoubtedly absorbed in the surface layers of both polymers, and we propose that while the longer wavelength components of the VUV‐radiation are absorbed by the bulk of the TrFE copolymer causing crosslinking, they are transmitted harmlessly in the PVDF homopolymer. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3253–3264, 2006 相似文献
17.
从实验上探讨了掺Nd^3+的氟化物玻璃光纤正向双程超荧光基本特性,包括输入-输出特性、输出-带宽特性以及输出-波长(激发)特性。并给出了理论上的拟合公式,实验表明利用氟化物玻璃光纤有望获得性能优异的有应用前景的低相干度集成化光源。 相似文献
18.
纳米NaYF4:Yb,Ho上转换荧光粉的合成及其性质研究 总被引:8,自引:0,他引:8
以EDTA为螯合剂,采用络合共沉淀法合成了纳米级镱、钬共掺杂的氟化钇钠上转换荧光材料.所合成的纳米材料颗粒均匀,分散性好.通过调节EDTA的加入量,可在41~148nm范围内调控纳米颗粒的大小.在980nm红外激光器照射下,肉眼可观察到明亮的上转换荧光,对发光机理进行了探讨. 相似文献
19.
PVDF/PAN共混超滤膜 总被引:11,自引:0,他引:11
PVDF/PAN共混超滤膜尹秀丽*宋艳秋(天津纺织工学院材料科学系天津300160)关键词聚偏氟乙烯,聚丙烯腈,共混,超滤膜1996-11-20收稿,1997-05-07修回共混是改变高分子材料性能的重要手段,已发现用聚合物共混的方法能制得性能优异的... 相似文献
20.