http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Li, Peng,Chen, Kuo,Zhao, Lili,Zhang, Hongyu,Sun, Haixiang,Yang, Xiujie,Kim, Nam Hoon,Lee, Joong Hee,Niu, Q. Jason Elsevier Science Ltd 2019 Composites Part B, Engineering Vol.166 No.-
<P><B>Abstract</B></P> <P>Hydrogen barrier properties are characteristic of polymeric materials prepared with graphene; thus, they can be considered as a good substitute for the metal body of the traditional hydrogen storage tank. Graphene oxide/polymer layer-by-layer self-assembling film based on noncovalent force shows good hydrogen gas barrier properties. However, the dense film structure can be broken when the film is placed in water environment, especially acidic or alkaline environment, which induces to the leak of the hydrogen gas. Herein, a modified graphene oxide/polyethyleneimine reactive layer-by-layer self-assembled film for the hydrogen barrier was fabricated by the covalent bond self-assembled technology. Graphene oxide was modified with ethylene glycol diglycidyl ether to introduce epoxy groups that can react with polyethyleneimine to form covalent bonds. The modification time, modification pH value, and the feed ratio of graphene oxide/ethylene glycol diglycidyl ether were investigated in detail. Results indicate that the self-assembled films were prepared by covalent bonds between polyethyleneimine and modified graphene oxide. When the modification time was 6 h, pH value was 2, and the feed ratio of graphene oxide/ethylene glycol diglycidyl ether was 0.05/0.23, the hydrogen transmission rate of 10-bilayer modified graphene oxide/polyethyleneimine self-assembled films was 289 cm<SUP>3</SUP>/m<SUP>2</SUP>·24 h·0.1 MPa, which was decreased by 78.8% compared to that of the polyethylene terephthalate substrate films (1365 cm<SUP>3</SUP>/m<SUP>2</SUP>·24 h·0.1 MPa). Furthermore, the modified graphene oxide/polyethyleneimine reactive layer-by-layer self-assembled films exhibit acid-resistance, alkali-resistance, salt-resistance and thermal-resistance properties.</P>
Research on Patchwork's Origin and Development
Wang, Jianping,Li, Xiujie,Mi, Jianuan The Costume Culture Association 2009 Fashion, industry and education Vol.12 No.1
Patchwork is a handicraft to put some certain shapes of small cloths together. Historical records of patchwork was discovered in Ancient Egypt as far back as BC 1000. Patchwork has been popular in the England and in around 13-$14^{th}$ century, European spliced little pieces of cloths for cold necessities, which made the handle of patchwork techniques gradually tend to decorative other than utility. Patchwork designs and techniques were taken across the Atlantic to North America with the early settlers in the mid-eighteenth century. In the early years of $20^{th}$ century, owing to the continuous technological advances, woman got more job opportunities that made patchwork technologies withered. Patchwork art continually evolved on the basis of historical and cultural factors to new styles, the famous Hawaiian, Stained Glass, Mola, Celtic, Victoria, Seminole and many other patchwork styles like that perfect embodied different art and cultures of different nations in different times.
Zhenhua Jiang,Xiujie Li,Shuling Zhang,Fugui Zhou,Jinhui Pang,Chunfeng Zhang,Dong Sun,Jianxin Mu,Guibin Wang 한국고분자학회 2011 Macromolecular Research Vol.19 No.5
Hyperbranched poly(ether ether ketone)s (HPEEKs) that were suitable as rheology control agents for linear poly(ether ether ketone)s (LPEEKs) were first prepared via commercially available hydroquinone (A2 monomer,HQ) and synthesized 3,4',5-trifluoro-benzophenone (BB'2 monomer, TF) effortlessly. The polymerization mode of A2 + BB'2 was demonstrated by MS. Moreover, FTIR, 1H NMR, 13C NMR, and 19F NMR spectroscopy revealed the structure and degree of branching (DB) of the resulting polymers. In comparison with A2 + B3 approach, HPEEK prepared using an A2 + BB'2 strategy possessed a higher molecular weight, and improved the melt processability of LPEEK. Remarkably, with the addition of HPEEK, the mechanical properties of LPEEK increased with a HPEEK content of 5%. The improved mechanical properties were attributed to the good miscibility. Moreover, the addition of HPEEK did not decrease the thermal stability of LPEEK.
Lei Lei,Yunhe Zhang,Xiujie Li,Jianxin Mu,Guibin Wang,Zhenhua Jiang,Shuling Zhang 한국고분자학회 2010 Macromolecular Research Vol.18 No.4
A novel hyperbranched poly(aryl ether ketone) terminated with cobalt phthalocyanine (CoPc-T-HPAEK)was prepared using 1,3,5-tris[4-(4-fluorobenzoyl) phenoxy] benzene (B3), as a ‘core’ molecule, 4,4'-(hexafluoroisopropylidene)diphenol (6F-BPA) as an A2 monomer, and cobalt phthalocyanine as an end-capping reagent. CoPc-THPAEK showed good solubility, thermal stability and catalytic activity in the oxidative decomposition of 2,4,6-trichlorophenol (TCP) under H2O2 or KHSO5. Moreover, the oxidative effect of KHSO5 was superior to that of H2O2,and the catalytic activity of CoPc-T-HPAEK was much higher than that of linear poly(aryl ether ketone) terminated with cobalt phthalocyanine (CoPc-T-LPAEK) and linear poly(aryl ether ketone) with a cobalt phthalocyanine pendant unit (CoPc-S-LPAEK).