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Jiaqi An Zongye Wang Shouhua Hui Ziyu Wang Yanwu Zhang 《Journal of polymer science. Part A, Polymer chemistry》2024,62(9):1890-1901
Dispersants play a significant role in the formulation of positive battery slurry. Adding a small amount of dispersant can effectively reduce the viscosity of the slurry, which is beneficial for the production of positive batteries. A series of copolymers of N-vinylpyrrolidone (NVP) and 2-ethylhexyl acrylate (2-EHA) with different molar ratios of NVP to 2-EHA, different polymer molecular weights and different polymer structures are synthesized by dl -methionine-mediated reversible deactivation radical polymerization. The ability of these copolymers to disperse LiFePO4 battery positive slurry with a high solid content (57.08%) as dispersants has been evaluated. Research shows that when the ratio of NVP to 2-EHA is 20 and the polymer molecular weight is 6000, poly(N-vinylpyrrolidone-ran-2-ethylhexyl acrylate) (NVP-ran-2-EHA) exhibits the strongest dispersing ability to the slurry. This polymer can reduce the viscosity of the slurry by 43.925% and has the longest stabilization time of 3 h, which is better than poly(N-vinylpyrrolidone) (PVP) and poly(N-vinylpyrrolidone)-block-poly(2-ethylhexyl acrylate) (PVP-b-PEHA) with the same molecular weight. 相似文献
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Journal of Thermal Analysis and Calorimetry - Alkali-activated materials are low-environmental-impact binders that can be obtained from the alkaline activation of industrial wastes. In this study,... 相似文献
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Li Guojin Li Qiang Ye Jianglin Fu Guangsheng Han JunJian Zhu Yanwu 《Journal of Solid State Electrochemistry》2017,21(11):3169-3177
Journal of Solid State Electrochemistry - Activated carbon has been synthesized from the waste filter carbon in household water purifier. The original waste filter carbon (OFC) gives poor specific... 相似文献
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Changxi Li Junpo He Yanwu Zhou Yuankai Gu Yuliang Yang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(6):1351-1360
Radical‐induced oxidation of reversible addition‐fragmentation chain transfer (RAFT) agents is investigated with respect to the effect of molecular structure on oxidation rate. The radicals are generated by homolysis of either azobisisobutyronitrile or alkoxyamine and transformed in situ immediately into peroxy radicals through transfer to molecular oxygen. It is found that the oxidation rate depends on the structure of Z‐ and R‐group of thiocarbonylthio compounds. For dithioesters with identical Z‐phenyl substituent, the oxidation rate decreases in the order of cyanoisopropyl (? C(Me)2CN) > cumyl (? C(Me)2Ph) > phenylethyl (? CH(Me)Ph) > 2‐methoxy‐1‐methyl‐2‐oxoethyl (? CH(Me) ? C(?O)OCH3) > benzyl (? CH2Ph). For dithioesters with identical R‐group, the oxidation rate decreases in the order of Z = phenyl? ~ benzyl? > RS? (trithiocarbonates) > RO? (xanthates). The stability of the RAFT agents toward oxidation correlates well with the chain transfer abilities as those previously reported by Rizzardo and coworkers. The priority of the oxidation reaction over the RAFT process, and the subsequent influence on RAFT polymerization are also investigated. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
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Yanwu Li 《Tetrahedron letters》2006,47(5):787-789
Kahweofuran, as an impact flavor component of roasted coffee and possesses the 6-methyl-2,3-dihydrothieno[2,3-c]furan structure, was rapidly synthesized from 2-acetyl-3-hydroxymethylthiophene by the formal reductive cyclization using the Wilkinson’s catalyst. Similarly, the syntheses of the 4-methyl, 6-ethyl and 4,6-dimethyl derivatives were also achieved in favorable yields. 相似文献