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关于个苯甲酸氧基苯甲酸(BBA)的合成虽已有报道[‘j,但其双分子缔合物具有液晶性则属本文作者首次发现.一般认为在有机分子结构中引人不对称性及柔性基团对其液晶性的形成十分重要“‘.在不具备这两个条件时,当分子的长径比达到一定值(约l/d>4)时也可能出现液晶性,但实例不多,且一般t。。很高.如聚合度为5的聚苯t。。一388”C[’j,而且难溶.这给此类液晶化合物的研究带来很大不便.BBA以双分子缔合物(BBA)。形式存在,结构对称,亦无柔性基团,但却具有液晶性,其t。。为230C.BBA与个乙酸氧基苯甲酸形成的低共熔… 相似文献
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4.2 Ruland方法使用式(2)计算结晶度时,Ruland考虑了热运动及晶格畸变的影响,从而使算得的结晶度值较合理。在不失计算结晶度W_(c,x)数值精度的情况下,在Ruland方法的实验中可以只取具有较大衍射峰强度的S范围,就可提高计算结晶度的数值准确性,克服了其它方法必须收集尽可能大范围S内的衍射强度数据的限制。Ruland方法测定结晶度的基本公式: 相似文献
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Jacob John Ramaswamy Mani Mrinal Bhattacharya 《Journal of polymer science. Part A, Polymer chemistry》2002,40(12):2003-2014
Three different biodegradable polyesters, namely, polycaprolactone (PCL), polybutylene succinate (BIONOLLE), and a copolyester of adipic acid, terephthalic acid, and 1,4‐butanediol (EASTAR) were melt‐blended using a twin‐screw extruder. The percentage composition of each of the aforementioned polymers was varied to obtain different blends, and the mechanical properties were evaluated. Selected blends showed significant improvement in tensile strength as compared with the individual polymers used to prepare the blend. The compatibility between the polymer phases was examined via Fourier transform infrared (FTIR) and nuclear magnetic resonace (NMR) spectroscopy as well as dynamic mechanical analysis. FTIR and NMR data confirmed the occurrence of hydrogen‐bonding and ester‐interchange reactions. Thermal properties and changes in crystallinity of the blends were examined with differential scanning calorimetry and X‐ray diffraction. A considerable increase in crystallinity was shown by the blend system containing BIONOLLE/PCL. The morphology of the blends was observed and correlated to the improved mechanical properties of the blend system. Results revealed an intermediate multiphase system in which a significant degree of mixing was achieved through the chemical interaction of the functional groups present, while using the twin‐screw extruder. Significant improvement in mechanical properties of some blends was observed, and information about the miscibility of these polyesters is provided. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2003–2014, 2002 相似文献
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C. D. Wingard 《Journal of Thermal Analysis and Calorimetry》1997,49(1):385-391
Eight samples from different areas of stretch-blow-molded poly(ethylene terephthalate) [PET] bottles, including a PET resin control, were tested by differential scanning calorimetry (DSC) and thermomechanical analysis (TMA). The glass transition temperature (T
g) was found to linearly decrease about 6C from zero to 45 percent initial crystallinity. Measurements ofT
c (crystallization temperature, DSC) and film tension modulus (TMA) were related to crystallization rate during stretch-blow-molding. The TMA linear coefficients of thermal expansion and shrinkage were shown to be important for blow-molding temperature control. 相似文献
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Qi-ding Mi Qi-feng Zhou Department of Polymer Science & Engineering College of Chemistry Peking University Beijing China 《高分子科学》2000,(2):139-148
Some new mesogen-jacketed liquid crystalline polymers (MJLCP) with polymer backbones, spacers, andmesogenic units of different structures were synthesized by radical polymerization. The mesomorphic behavior of thesepolymers was examined using differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). Theirliquid crystallinity is influenced by the variation of polymer backbone, spacer, mesogenic unit and its terminal groups. Theresults show that 1) a more flexible polymer main-chain is more favorable to the formation of a liquid crystal phase, while 2)a flexible spacer will decrease the "Jacket Effect" and the liquid crystallinity and 3) a subtle modification of the terminalgroups on the mesogenic unit may also have a significant influence on properties of the polymers. 相似文献
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Crystallinity and crystalline phase orientation of poly(1,4‐cis‐isoprene) from Hevea brasiliensis and Taraxacum kok‐saghyz
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Sara Musto Vincenzina Barbera Mario Maggio Marco Mauro Gaetano Guerra Maurizio Galimberti 《先进技术聚合物》2016,27(8):1082-1090
Crystallization is studied for poly(isoprene‐1,4‐cis) from Hevea brasiliensis (natural rubber [NR]) and from taraxacum kok‐saghyz, mainly by collecting wide‐angle X‐ray diffraction patterns after processing and stretching. Although rubber samples before stretching are generally fully amorphous, crystallization can be induced in NR samples by processing at room temperature under moderate pressure. This phenomenon is possibly associated with nucleation by saturated fatty acid components. For rubber samples being fully amorphous in the undeformed state, strain‐induced crystallization occurs only at high strain ratios (α > 4), leading to high degrees of crystalline phase orientation (fc > 0.9 for α = 5). Rubber samples presenting some crystallinity already in the unstretched state, on the contrary, reach much lower degrees of axial orientation, even for high strain ratios (fc < 0.7 for α = 5). These differences in crystallinity and in crystalline phase orientations produce large differences in stress–strain behavior of the rubber. By room temperature processing, the considered NR samples can also develop an unreported disordered crystalline modification, with low intensity of 120 and 121 reflections. This disordered crystalline modification, which is also maintained after axial stretching procedures, can rationalized by a structural disorder along the b axis, possibly associated with statistical sequences of A+TA? or A?T A+ conformations for poly(isoprene‐1,4‐cis) chains. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
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