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61.
动态硫化EPDM/PP共混体系中PP相的结晶度及晶体结构的研究 总被引:3,自引:0,他引:3
研究了动态硫化EPDM/PP共混物中PP相的结晶度及晶体结构,同时讨论了制备工艺条件以共混物中PP相的结晶度和晶体结构的影响。结果表明:在动态硫化EPDM/PP共混物中,硫化的EPDM的分子键没有穿入PP的晶区,PP的结晶度随EPDM含量的增加而下降。提高共混温度,加入软化剂或碳黑均使共混物中PP的结晶度降低,共混时间15min时,共混物中PP相的结晶度最低,但PP的晶格不受制备工艺条件的影响。 相似文献
62.
van Miltenburg J. C. Mathot V. B. F. van Ekeren P. J. Ionescu L. D. 《Journal of Thermal Analysis and Calorimetry》1999,56(3):1017-1023
The heat capacity of a very low-density polyethylene copolymer (VLDPE) was measured between 10 and 410 K. Using two sets of
literature data for the fully crystalline and the fully amorphous states, crystallinities were calculated as a function of
temperature. During the stabilisation periods in the melting process no equilibrium is reached, because of an exothermic process,
which is attributed to (re)crystallization. Values for the enthalpy of melting and for the heat capacity of the liquid are
given.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
63.
Harumi Sato Rumi Murakami Jianming Zhang Katsuhito Mori Isao Takahashi Hikaru Terauchi Isao Noda Yukihiro Ozaki 《Macromolecular Symposia》2005,230(1):158-166
Infrared (IR) spectra and wide-angle X-ray diffraction (WAXD) patterns of poly(3-hydroxybutyrate) (PHB) and its copolyester, poly(3-hydroxybutyrate-co-3-hydroxyhexanoate), P(HB-co-HHx) (HHx = 12 mol%) were measured over a temperature range of 20 °C to higher temperatures (PHB, 185 °C, HHx = 12 mol%, 140 °C) to explore their structure change and thermal behavior and molecular interaction. The WAXD measurements revealed that the a lattice parameter increases significantly with temperature, while the b lattice parameter varies a little in the crystalline PHB and P(HB-co-HHx). It seems that the intermolecular interaction between the CO group of one helical structure and the CH3 group of the other helical structure decreases along the a axis of crystalline PHB and P(HB-co-HHx) with temperature. The temperature-dependent IR spectral variations were analyzed for the CH stretching, CO stretching, CH3 deformation, and C O C stretching variation regions, and bands characteristic of crystalline and amorphous parts were identified in each region. It was found from the anomalous frequencies of the CH3 asymmetric stretching and CO stretching bands of PHB and P(HB-co-HHx) and the X-ray crystallographic structure of PHB that there is an intermolecular interaction (C H…OC hydrogen bond) between the CO group and the CH3 group combining two helical structures in PHB and P(HB-co-HHx). In this review paper we discuss the role of the C H…OC hydrogen bonding and the crystal and lamella structure of PHB and P(HB-co-HHx) (HHx = 12 mol %) in comparison with the structure of Nylon. 相似文献
64.
Heiko Winter Abdellatif Barakat Bernard Cathala Bodo Saake 《Macromolecular Symposia》2005,232(1):74-84
The sorption of arabinoxylan (AX) on bacterial cellulose was investigated by adding AX to the culture medium of Gluconacetobacter xylinus. The starting AX material was produced by alkaline extraction of oat spelts. To investigate the impact of varying AX quality, the residual lignin was reduced by ClO2 bleaching. Furthermore, bleached and unbleached xylans were subjected to xylanase hydrolysis in order to produce fractions of varying molar mass. Of all samples only the water soluble fractions were used for sorption experiments. A reduced molar mass resulted in a lower sorption of AX to the cellulose, while the lignin content increased the sorption of AX on bacterial cellulose. The sorption of AX resulted in a reduction of bacterial cellulose crystallinity and cellulose Iα content. In combined treatments of AX with xyloglucan and β-glucan no synergistic effect of those polysaccharides on the AX sorption was found. 相似文献
65.
M. L. Cerrada R. Benavente E. Prez J. M. Perea 《Journal of Polymer Science.Polymer Physics》2000,38(4):573-583
Vinyl alcohol–ethylene (VAE) copolymers, commercially manufactured by hydrolysis of the corresponding vinyl acetate–ethylene copolymers, can contain small amounts of unhydrolyzed vinyl acetate. This article shows the influence of these residual groups on the structure of the resulting copolymers, studied by nuclear magnetic resonance and wide‐angle X‐ray scattering. Thermal and mechanical properties of these materials were investigated by differential scanning calorimetry, thermogravimetry, drawing behavior, birefringence measurements, and dynamic mechanical analysis. The structure of the copolymers is considerably affected by the volume of the residual acetate groups, bigger than that of the hydroxyl ones, which hinders the crystallization process. In relation to the thermal and mechanical properties, the temperature and enthalpy of melting as well as the Young's modulus and yield stress, decrease as vinyl acetate molar fraction increases. Moreover, the α and β relaxations are shifted to lower temperatures as residual content in the copolymer is raised. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 573–583, 2000 相似文献
66.
The influence of aluminum borate whiskers upon the morphology of polyamide 6 was studied by wide-angle X-ray scattering and by differential scanning calorimetry. The whiskers did not promote the formation of either the hexagonal γ or the monoclinic β crystalline phase. A new experimental procedure has been devised for the production of very thin polymer layers on the whiskers. In the procedure, styrene co-acrylonitrile polymer is used as a processing aid and is later extracted. The procedure allows for the generation of polyamide layers less than 30 nm thick. Crystallinity in these thin layers was suppressed. An expression has been developed to characterize the crystallinity gradient in the interphase of the whisker surface. The equation shows that the initial 1.4 nm of polymer is fully amorphous and produces excellent evaluations of the crystallinity gradient to layer thicknesses of 70 nm. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35 : 2457–2464, 1997 相似文献
67.
Jae‐Yong Song Yong‐Kuk Yun Jung‐Il Jin 《Journal of polymer science. Part A, Polymer chemistry》1999,37(7):881-889
Two series of new wholly aromatic thermotropic copolyesters containing the 2‐(α‐phenylisopropyl)hydroquinone (PIHQ) moiety have been synthesized and their basic properties such as glass transition temperature (Tg), melting temperature (Tm), thermal stability, crystallinity, and liquid crystallinity were studied by differential scanning calorimetry (DSC), thermogravimetry (TG), and wide‐angle X‐ray diffractometry (WAXD) and on a polarizing microscope. The first series was prepared from acetylated PIHQ, terephthalic acid (TPA), and 2,6‐naphthalenedicarboxylic acid (NDA), and the second series from acetylated PIHQ, TPA, and 1,1′‐biphenyl‐4,4′‐dicarboxylic acid (BDA). The Tg values (152–168°C) of the two series are not much different, although the values for the first series appear slightly higher. The Tm values (287–378°C) and the degree of crystallinity of the first series are appreciably greater than those of the second series. Such differences can be explained by the geometric structure of NDA and BDA moieties. All of the present polyesters are thermotropic and nematic. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 881–889, 1999 相似文献
68.
Gaetano Guerra Odda Ruiz De Ballesteros Vincenzo Venditto Maurizio Galimberti Franco Sartori Rachele Pucciariello 《Journal of Polymer Science.Polymer Physics》1999,37(11):1095-1103
Structural (X‐ray diffraction), melting (differential scanning calorimetry), as well as mechanical (tensile tests) characterizations on uncrosslinked ethene–propene copolymer samples, obtained using a metallocene‐based catalytic system and having an ethene content in the range 80–50% by mol, are reported. Samples with an ethene content in the range 80–60% by mol present a disordered pseudohexagonal crystalline phase, whose melting moves from ≈ 40°C down to ≈ −20°C as the ethene content is reduced. The dramatic influence of the crystalline phase on tensile properties of uncrosslinked ethene–propene copolymers is shown. In particular, highest elongation at break values are obtained for samples being essentially amorphous in the unstretched state and partially crystallizing under stretching. On the other hand, lowest tension set values (most elastic behavior) are observed for samples presenting, already in the unstretched state, microcrystalline domains acting as physical crosslinks in a prevailing amorphous phase. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1095–1103, 1999 相似文献
69.
Subhash Chandra S. Annapoorni R. G. Sonkawade P. K. Kulriya Fouran Singh D. K. Avasthi J. M. S. Rana R. C. Ramola 《Indian Journal of Physics》2009,83(7):943-947
High-energy ion beam irradiation of the polymers is a good technique to modify the properties such as electrical conductivity,
structural behaviour and mechanial properties. Polyaniline thin films doped with hydrochloric acid (HCl) were prepared by
oxidation of ammonium persulphate. The effect of Swift Heavy Ions irradiation on the electrical and structural properties
of polyaniline has been measured in this study. Polyaniline films were irradiated by oxygen ions (energy 80 MeV, charge state
O+7) with fluence varying from 1 × 1010 to 3 × 1012 ions/cm2. The studies on electrical and structural properties of the irradiated polymers were investigated by measuring V-I using
four probe set-up and X-ray diffraction (XRD) using Bruker AXS, X-ray powder diffractometer. V-I measurements shows an increase
in the conductivity of the film, XRD pattern of the polymer shows that the crystallinity improved after the irradiation with
Swift Heavy Ions (SHI), which could be attributed to cross linking mechanism.
相似文献
70.
Kazuo Akagi 《Journal of polymer science. Part A, Polymer chemistry》2009,47(10):2463-2485
We review advances in liquid crystalline (LC) conjugated polymers by focusing on (i) ferroelectric and (ii) photoresponsive LC conjugated polymers. In Part 1, LC polyphenylene derivatives were synthesized through substitution of fluorine‐containing chiral LC groups into side chains. Poly(para‐phenylene) [ P1 ] and poly(meta‐phenylene) [ P2 ] derivatives showed chiral smectic C phases responsible for ferroelectricity. They exhibited quick response to electric field, giving switching times of <1 s between two bistable states. The spontaneous polarization (PS) of P2 remained unchanged even after the electric field became zero, affording the residual polarization (PR) whose value was the same as that of PS. This indicates that P2 has a potential memory function based on FLC nature. In Part 2, poly(para‐phenylenevinylene) [ P5 ] and poly(bithienylene‐phenylene) [ P6 ] derivatives were synthesized by introducing dithienylethene moieties into side chains. Drastic quenching of fluorescence occurred when the photoresponsive moiety changed from an open form to a closed one upon an irradiation of ultraviolet light. The quenched fluorescence was recovered through a photoisomerization from the closed form to the open one. Macroscopically aligned P6 film exhibited a linearly polarized fluorescence with significant anisotropy. Reversible quenching and emitting behavior in anisotropic fluorescence was controlled by the photochemical switching. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2463–2485, 2009 相似文献