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1.
Cellulose carbamate, an environmentally friendly material presents an interesting alternative to petroleum-based polymers because of its renewable, biodegradable, biocompatible nature and its solubility in conventional solvents. In synthesis process of cellulose carbamate, urea was firstly impregnated into the cellulose pulp by supercritical CO2(scCO2), followed by the esterification of cellulose. The structure of cellulose carbamate was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) and scanning electron microscopy (SEM). The rheological properties of these cellulose carbamates in 9% sodium hydroxide solution were investigated, using a range of the nitrogen content, concentrations and shear rates. 相似文献
2.
R. Cressely V. Hartmann 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,6(1):57-62
In this experimental work we carefully investigate the rheological behaviour and in particular the shear thickening exhibited
by aqueous micellar solutions of CTAB with NaSal as added counterion. We are particularly interested in the evolution of the
critical shear rate (at which shear thickening occurs) versus
C
D
, the surfactant concentration. We show that , at fixed salt concentration C
S
, increases with C
D
following a power law evolution with a positive exponent of + 5.8. On the other hand we show that if the ratio C
D
/ C
S
is fixed, decreases with C
D
with a negative exponent of -2.0. Nevertheless investigations of the zero shear viscosity indicate that in all situations (implying variation of the surfactant concentration C
D
, or the salt concentration C
S
or the temperature) is a decreasing function of the length of the micelles. All these evolutions are compatible with a gelation mechanism which
could possibly be associated with entanglement effects of large interacting flowing structures.
Received: 3 March 1998 / Revised: 16 June 1998 / Accepted: 3 July 1998 相似文献
3.
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5.
Various diblocks, triblocks and a graft copolymer of butadiene with 4-vinylpyridine short blocks have been prepared. They were complexed with ZnCl2 to give ionomer-like materials. For all copolymers, the Tg of the elastomeric block (?84°C to ?91°C) was unchanged by complexation. For all diblocks and triblocks with short blocks (DP n ~ 3) the storage modulus was only slightly increased by comparison with uncomplexed materials. For the graft copolymer even with short blocks the material is less sensitive to temperature after complexation. For triblocks, when the DP n of the vinylpyridine blocks was high enough (15 units), complexes were associated in multiplets of large size and the elastomeric properties were retained up to 200°C. 相似文献
6.
Effects of polystyrene-encapsulated magnesium hydroxide on rheological and flame-retarding properties of HIPS composites 总被引:1,自引:0,他引:1
In this study, polystyrene (PS)-encapsulated magnesium hydroxide (Mg(OH)2) was successfully prepared by in situ polymerization of styrene on the surface of Mg(OH)2 in a high-speed mixer. A large amount of PS chemically bonded on Mg(OH)2 surface was confirmed by means of FT-IR, TGA and SEM. A series of composites of high impact polystyrene (HIPS) were prepared by melt blending in a co-rotating twin-screw extruder. The effects of PS-encapsulated filler on the properties of HIPS composites were studied by SEM, rheology and combustion tests (horizontal burning tests and cone calorimetry). The dispersion and adhesion patterns of PS-encapsulated Mg(OH)2 in HIPS matrix were investigated through FT-IR and SEM. The experimental results demonstrated that comparing to the composites containing untreated filler, the rheological and flame retardant properties of those containing PS-encapsulated filler were found to be significantly improved. This improvement is mostly attributed to a better dispersion of the encapsulated filler and a strong adhesion between the filler and matrix. 相似文献
7.
Wen-Jia Zhou Shu-Juan Bao Yan-Yu Liang Ben-Lin He Hu-Lin Li 《Journal of Solid State Electrochemistry》2006,10(5):277-282
Pure-phase and well-crystallized spinel LiMn2O4 powders were successfully synthesized by a simple rheological phase method. The thermal behavior and structure properties
of the powders prepared by the rheological phase method compared with the solid-state reaction were investigated by thermogravimetry,
powder X-ray diffraction , scanning electron microscopy and transmission electron microscopy. According to the results of
the electrochemical tests, it is obvious that the sample resulting from the rheological phase method shows higher discharge
capacity and better cycling stability than one formed in the solid-state reaction. The cyclic voltammogram and columbic efficiency
curves also confirm that the product by the rheological phase method has a good cycling performance due to its fine cubic
spinel structure and morphology. 相似文献
8.
9.
不同类型聚合物溶液对采油残余油的作用机理研究 总被引:6,自引:0,他引:6
通过实验测定了HPAM溶液和黄原胶溶液的流变性、在多孔介质中的流变性和残余阻力系数 ,计算了衰竭层效应 .用不同的浓度和注入速度进行了驱油实验 .提出聚合物分子缠结作用的增强不仅引起表观粘度增加或衰竭层厚度降低 ,而且使平行于油水界面的拉动残余油的力增加 ,从而使残余油饱和度降低 ,采收率提高 .随浓度增加 ,HPAM溶液的表观粘度和残余阻力系数增加 ,衰竭层厚度减小 ;黄原胶溶液的浓度高于缠结浓度时 ,衰竭层厚度和表观粘度变化不大 .注入速度增加时 ,两种聚合物溶液的衰竭层厚度均降低 ,HPAM溶液的残余阻力系数不变 ,粘弹性增加 ;而黄原胶溶液的残余阻力系数下降 .不同浓度和注入速度情况下两种聚合物溶液的驱油结果证实了文中提出的聚合物分子缠结作用和衰竭层效应对残余油的作用机理 .分子结构的不同是造成两种聚合物溶液在多孔介质中渗流规律和对残余油作用机理的差别的根本原因 . 相似文献
10.
相反转技术制备环氧树脂水基体系——相反转过程的流变行为研究 总被引:18,自引:0,他引:18
对高乳化剂浓度下的相反转发展过程的流变行为进行了应力扫描、动态频率扫描实验表征.结果表明,乳化剂浓度较高时,体系发生完全相反转;体系在相反转点前为W/O结构,其粘度几乎不随剪切应力的改变而改变,表现为牛顿流体行为;体系在相反转点后为O/W结构,具有很高的粘弹性,并且在较高剪切应力下表现为典型的假塑性.这是由于高分子水基微粒间通过其表面覆盖的表面活性剂与水形成氢键而产生了一种静态结构,此结构在较高剪切应力作用下破坏而导致假塑性. 相似文献