全文获取类型
收费全文 | 220篇 |
免费 | 16篇 |
国内免费 | 28篇 |
专业分类
化学 | 171篇 |
晶体学 | 4篇 |
力学 | 28篇 |
综合类 | 4篇 |
物理学 | 57篇 |
出版年
2023年 | 1篇 |
2022年 | 5篇 |
2021年 | 11篇 |
2020年 | 19篇 |
2019年 | 10篇 |
2018年 | 6篇 |
2017年 | 14篇 |
2016年 | 9篇 |
2015年 | 9篇 |
2014年 | 11篇 |
2013年 | 22篇 |
2012年 | 2篇 |
2011年 | 14篇 |
2010年 | 13篇 |
2009年 | 11篇 |
2008年 | 21篇 |
2007年 | 12篇 |
2006年 | 13篇 |
2005年 | 10篇 |
2004年 | 7篇 |
2003年 | 9篇 |
2002年 | 10篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1997年 | 4篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1993年 | 1篇 |
1992年 | 1篇 |
1988年 | 1篇 |
1987年 | 1篇 |
1985年 | 1篇 |
排序方式: 共有264条查询结果,搜索用时 31 毫秒
1.
Yogesh Patil George Zapsas Yves Gnanou Nikos Hadjichristidis 《Journal of polymer science. Part A, Polymer chemistry》2020,58(1):163-171
This study presents the synthesis and properties of linear PVDF-based amphiphilic triblock terpolymers with PS and PEO, [PVDF-b-PS-b-PEO], by adopting a procedure that involves: (a) iodine-transfer polymerization (ITP) of VDF with 1-iodoperfluorohexane (C6F13I) serving as chain-transfer agent (CTA) to afford C6F13-PVDF-I, (b) ITP of styrene with the C6F13-PVDF-I macromolecular-CTA to obtain C6F13-PVDF-b-PS-I diblock copolymer, (c) end-group exchange from iodo- to azido-group by nucleophilic substitution reaction with NaN3, and (d) copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-terminated PEO to achieve C6F13-PVDF-b-PS-b-PEO triblock terpolymers. The 1H and 19F NMR spectroscopy confirmed the presence of all blocks, while gel permeation chromatography traces showed the living nature of ITP technique. The self-assembly of these terpolymers was investigated in films (atomic force microscopy and DSC), as well as in aqueous and organic solvents (DLS). The analysis of crystalline phases based on the FTIR spectroscopy indicated the conversion of PVDF α-phase into α + β-phases and β + γ-phases upon the incorporation of PS and PEO blocks, respectively. The synthesized amphiphilic copolymers were evaluated (fluorescence spectroscopy) as carriers of small hydrophobic molecules in water. © 2019 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 163–171 相似文献
2.
Jun-Feng Liu Zhan-Yu Wu Dr. Florian J. Stadler Dr. Yan-Fei Huang 《Angewandte Chemie (International ed. in English)》2023,62(26):e202300243
Ionic liquids (ILs)-incorporated solid-state polymer electrolytes (iono-SPEs) have high ionic conductivities but show non-uniform Li+ transport in different phases. This work greatly promotes Li+ transport in polymer phases by employing a poly (vinylidene fluoride-trifluoroethylene-chlorotrifluoroethylene) [P(VDF-TrFE-CTFE), PTC] as the framework of ILs to prepare iono-SPEs. Unlike PVDF, PTC with suitable polarity shows weaker adsorption energy on IL cations, reducing their possibility of occupying Li+-hopping sites. The significantly higher dielectric constant of PTC than PVDF facilitates the dissociation of Li-anions clusters. These two factors motivate Li+ transport along PTC chains, narrowing the difference in Li+ transport among varied phases. The LiFePO4/PTC iono-SPE/Li cells cycle steadily with capacity retention of 91.5 % after 1000 cycles at 1 C and 25 °C. This work paves a new way to induce uniform Li+ flux in iono-SPEs through polarity and dielectric design of polymer matrix. 相似文献
3.
Pristine multi-walled carbon nanotubes (MWNTs) were incorporated into poly(vinylidene fluoride) (PVDF), poly(methyl methacrylate) (PMMA), and PVDF/PMMA blends to achieve binary and ternary nanocomposites. MWNTs were more compatible with the PVDF matrix than with the PMMA-containing matrices. MWNT addition did not alter the development of α-form PVDF crystals in the binary/ternary composites. Nucleation and overall isothermal crystallization of PVDF were enhanced by the presence of MWNTs, and enhancements were optimal in the PVDF/MWNT binary composites. Avrami analysis revealed that addition of MWNTs led to more extensive athermal-type nucleation of PVDF, and that PMMA slightly decreased the crystal growth dimension of PVDF. The equilibrium melting temperature (Tm°) of PVDF increased in the binary composites but remained nearly constant in the ternary system. Thermal stability was enhanced in the binary/ternary composites, and enhancements were more evident in the air environment than in nitrogen. Rheological property measurements revealed that the intensely entangled chains of high-molecular weight PVDF dominated the rheological response of PVDF-included samples in the melt state. A (pseudo)network structure was developed in each of the PVDF-included samples as well as in the 1 phr MWNT-added PMMA/MWNT composite. The storage moduli of the PVDF, PMMA, and PVDF/PMMA:1/1 blend increased to 37%, 22% and 34%, respectively, at 40 °C after addition of 1 phr MWNT. 相似文献
4.
以碳纤维(CF)为填料,聚偏氟乙烯(PVDF)为基体,通过熔融共混法制备PVDF/CF导电复合材料.所得复合材料具有显著的正温度系数(PTC)效应,温度上升到聚合物熔点附近时,电阻率对温度变化敏感.在转折温度区间(155.5~171.0oC,(35)(28)15.5oC)内,其体积电阻率的增加速率约为1.3×105?cm K-1.在不同CF含量下,复合材料表现出不同的PTC行为.随着CF含量的增加,其峰值电阻略有下降.高导电粒子含量下,无负温度系数(NTC)效应.在冷却循环过程,导电网络的重构性良好.复合材料即使经过多次热循环,依然表现出良好的PTC特性重现性. 相似文献
5.
6.
Sandrine?Chaput Christian?CarrotEmail author Mickael?Castro Frederic?Prochazka 《Rheologica Acta》2004,43(5):417-426
The work focuses on the detection of the co-continuity window in immiscible polymer blends. The purpose of the paper is to describe how rheological techniques can help to evaluate the composition range of the co-continuous morphology through the study of a particular system: PEO/PVDF-HFP. First, the blends were characterized by selective dissolution experiments and SEM observations. Then the ability of dynamic mechanical spectroscopy to detect the co-continuity was investigated in the melt and in the solid state. The evolution of the storage modulus of molten blends with their composition at a constant low frequency gives information about the co-continuity interval, especially as far as the onset of the continuity of the PEO phase is concerned. Then the immiscibility of the polymers and the continuity of PVDF-HFP as a function of blend composition have been highlighted by means of dynamic mechanical spectrometry below the melting point of PVDF-HFP. Comparison with results from classical methods shows fair agreement.This paper was presented at the first Annual European Rheology Conference (AERC) held in Guimarães, Portugal, September 11-13, 2003. 相似文献
7.
用PVDF实时测量激光诱导的冲击波压力 总被引:4,自引:1,他引:4
本文用自己研制的PVDF(polyvenylidenfluoride)压电传感器测量了0.2mm厚铝和2.08mm厚T300/环氧复合材料中激光诱导的冲击波压力,首次获得了这些材料中激光冲击波压力的时间演化波形。实验在中国科大强激光实验室的YAG脉冲激光器上进行,激光波长1.06μm,脉宽33ns,靶面平均功率密度为109W/cm2量级。从所得数据估计了表面入射压力,其值与已有结果符合良好。实验结果证实,PVDF压电传感器频响高,量程宽,多次使用重复性好,可有效应用于激光冲击波压力的实时测量 相似文献
8.
Aline Bruna da Silva Juliano Marini Genaro Gelves Uttandaraman Sundararaj Rinaldo Gregório Jr. Rosario E.S. Bretas 《European Polymer Journal》2013
The objective of this work was to prepare novel conductive blends of poly(vinylidene fluoride) (PVDF) with polypyrrole (PPy) and to compare their performance with PVDF/multiwall carbon nanotube (MWCNT) composites and novel PVDF/PPy/MWCNT hybrid systems. All the compositions were prepared by melt mixing using a miniature mixer. The mixtures were characterized by Fourier transformed infrared (FTIR), wide angle X-ray diffraction (WAXD), thermogravimetric analyses (TGA), scanning and transmission electron microscopy (SEM and TEM, respectively) and volume electrical resistivity. For the binary PVDF/PPy and PVDF/MWCNT systems, percolation thresholds of 10 and 0.3 wt%, respectively, were found. In the hybrid systems, however, the percolation threshold for each filler was lower than in the binary systems, but the electrical conductivities were always much higher at all concentrations than the conductivities of the binary systems. Therefore, the addition of both fillers had a synergistic effect on the hybrid system conductivity, which was attributed to its morphology: the PPy increased the homogeneity of the MWCNT distribution and decreased the available free volume for the MWCNT; as a result the MWCNT rolled around the PPy particles bridging them through the PVDF matrix, increasing the quantum tunneling effect and thus, the electrical conductivity of the system. 相似文献
9.
Nelaka Govinna Ilin Sadeghi Ayse Asatekin Peggy Cebe 《Journal of Polymer Science.Polymer Physics》2019,57(6):312-322
We report the structure and thermal properties of blends comprising poly(vinylidene fluoride) (PVDF) and a random fluorinated copolymer (FCP) of poly(methyl methacrylate)‐random‐1H,1H,2H,2H‐perfluorodecyl methacrylate, promising membrane materials for oil–water separation. The roles of processing method and copolymer content on structure and properties were studied for fibrous membranes and films with varying compositions. Bead‐free, nonwoven fibrous membranes were obtained by electrospinning. Fiber diameters ranged from 0.4 to 1.9 μm, and thinner fibers were obtained for PVDF content >80%. As copolymer content increased, degree of crystallinity and onset of degradation for each blend decreased. Processing conditions have a greater impact on the crystallographic phase of PVDF than copolymer content. Fibers have polar beta phase; solution‐cast films contain gamma and beta phase; and melt crystallized films form alpha phase. Kwei's model was used to model the glass transition temperatures of the blends. Addition of FCP increases hydrophobicity of the electrospun membranes. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 312–322 相似文献
10.