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991.
A new type of polyimide foam (PIF) was prepared and characterized based on a one‐pot process by the reaction of a first solution with different ratios of a second solution. The first solution was comprised of pyromellitic dianhydride (PMDA), N, N‐dimethyl formamide (DMF), methanol, water, surfactant, and catalysts, while the second solution contained polyaryl polymethylene isocyanate (PAPI). In the present study, the relationships among compositions, structures, and properties of PIFs were investigated. The results indicated that with the increase in the weight ratio of PAPI/(first solution), the foaming degrees of PIFs increased from 10.14 to 10.52 times and the apparent densities before postcure decreased from 15.96 to 14.51 kg/m3. The open cell contents, average sound absorption coefficients, and average cellular diameters of PIFs after postcure increased with increase in the weight ratio of PAPI/(first solution). The glass transition temperatures (Tg) of PIFs after postcure first increased from 287 to 299°C, then decreased to 292°C, and the 5% weight loss temperatures and 10% weight loss temperatures presented the same trend as well. The compressive and flatwise tensile properties scaled very well with the relative densities of the foams after postcure, with the highest compressive strength of 0.03 MPa and the highest flatwise tensile strength of 0.15 MPa. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
992.
993.
994.
偏钒酸铵催化合成2-芳基取代苯并噁唑 总被引:2,自引:0,他引:2
在偏钒酸铵催化下,以2-氨基苯酚和芳醛为原料、乙醇为溶剂,在室温下合成了一系列2-芳基取代苯并噁唑类化合物.该方法具有操作简便、反应条件温和、产率高等优点. 相似文献
995.
996.
Three new compounds, 2‐methoxy‐3,4‐(methylenedioxy)benzophenone ( 1 ), 4‐hydroxy‐2,3‐dimethoxybenzophenone ( 2 ), and 3‐hydroxy‐4,6‐dimethoxy‐9H‐xanthen‐9‐one ( 3 ), besides three known compounds were isolated from the roots of Securidaca inappendiculata. Their structures were established by spectroscopic means and X‐ray crystallographic diffraction analysis. The biogenetic relationships among these six compounds are discussed. 相似文献
997.
998.
Systematic NMR characterization of 4‐thio‐5‐furan‐pyrimidine nucleosides or 4‐thio‐5‐thiophene‐pyrimidine nucleosides (ribonucleosides and 2′‐deoxynucleosides) was performed. All proton and carbon signals of 4‐thio‐5‐thiophene‐ribouridine and related analogues were unambiguously assigned. The orientations of the base (4‐thiouridine or its deoxy analogue) relative to the ring (furan or thiophene) are explored by a NMR approach and further supported by X‐ray crystallographic studies. The procedures presented here would be applicable to other modified nucleosides and nucleotides. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
999.
1000.
L LinHui Ye YanLin Jiang DongXing Hua Hui Zheng Tao Li ZhiHuan Ge YuCheng Li XiangQing Lou JianLing Cao ZhongXin Song YuShou Xiao Jun Li QiTe Qiao Rui You HaiBo Chen RuiJiu Xu HuShan Wang JianSong Guo ZhongYan Zhang XueYing Li Chen Hu ZhengGuo Chen RuoFu Wang Meng Xu ZhiGuo Yue Ke Tang Bin Zang YongDong Zhang XueHeng Yao XiangWu Chen JinDa Bai Zhen 《中国科学:物理学 力学 天文学(英文版)》2011,54(1):136-140
Knockout reaction experiment was carried out by using the 6He beams at 61.2 MeV/u impinging on a CH2 target. The α core fragments at forward angles were detected in coincidence with the recoiled protons at larger angles. From this exclusive measurement the valence nucleon knockout mechanism and the core knockout mechanism can be distinguished by the relation between the polar angles of the core fragments and the recoiled protons, respectively. It is demonstrated that the core knockout mechanism may result in some strong contamination to the real invariant mass spectrum.
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