期刊文献+

聚氯代对二甲苯膜的退火处理及热氧老化研究 被引量:1

Anneal Treatment and Thermal Oxidation Aging Study of Poly(chloro-para-xylylene) Films
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摘要 采用化学气相沉积法制备聚氯代对二甲苯(PPXC)膜,并对其在氩气和空气2种气氛中进行退火处理,研究退火前后PPXC膜的微观结构、拉伸强度及水汽渗透率变化。结果表明,PPXC膜在2种气氛下恒温退火,聚合物的结构变化存在2个过程,结晶完善过程与降解过程,在大气中氧的存在增大了降解程度。PPXC膜的拉伸强度随退火时间先增大、后减小,而水汽渗透速率则随退火时间先减小、后增大。且在氩气气氛中,PPXC膜所达到的力学性能、水汽阻隔性能更佳。 Poly(chloro-para-xylylene) films were prepared through chemical vapor deposition method, which were annealed at the atmospheres of argon and air. The microstructure, tensile strength, moisture permeation rate of the films were analyzed . The results show that two obvious stages can be inferred for the whole annealing process. The first is the process of crystallization, and the second is the process of thermal degradation. The oxygen accelerates degradation process of the films. The tensile strength increases with the anneal time firstly, then decreases, however, the moisture permeation rate decreases firstly, then increases. The favorable mechanical and moistureproof properties of the films can be gained after annealing in the atmosphere of argon.
出处 《现代塑料加工应用》 CAS 北大核心 2009年第2期20-23,共4页 Modern Plastics Processing and Applications
关键词 聚氯代对二甲苯膜 退火处理 拉伸强度 水汽渗透率 poly(chloro-para-xylylene) films anneal treatment tensile strength moisture permeability
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  • 1Zhang X, Darbral S, Chiang C, et al. Crystallinity properties of parylene affecting its use as an ILD in submicron integrated circuit technology. Thin Solid Films, 1995,270 (1- 2) : 508-511
  • 2Senkevich J J, Desu S B. Morphology of poly(chloro-p-xylylene) CVD thin films. Polymer, 1999, 40(21): 5 751- 5 759
  • 3Ganguli S, Agrawal Hemant, Wang Bin, et al. Improved growth and thermal stability of parylene films. Vac Sci Technol, 1997,15(6): 3 138-3 142
  • 4Nowlin T E, Smith D F, Cieloszyk G S. Thermal oxidative stability of poly-p-xylylenes. Journal of Polymer Science, 1980,18(6): 2 103-2 119
  • 5Baker T E, Fix G L, Judge J S. Modified poly-para-xylylene coatings and films with improved oxidation resistance. J Electrochem Soc, 1980, 127(10): 1 851
  • 6Gorham W F. Para-xylylene polymers. US, US 3342754. 1967
  • 7Surendran G, Gazicki M, James W J. Polymerization of para-xylylene derivatives. V. Effects of the sublimation rate of di-p-xylylene on the crystallinity of parylene deposited at different temperatures. Journal of Polymer Science (Part A) : Polymer Chemistry, 1987, 25(8) : 2 089- 2 106
  • 8刘景江.高聚物的等温结晶[J].高分子材料科学与工程,1994,10(3):1-7. 被引量:5
  • 9张颖,王志,王世昌.高分子膜结构对气体传递的影响[J].高分子材料科学与工程,2004,20(4):24-27. 被引量:14

二级参考文献20

  • 1刘景江.马来酸酐接枝聚丙烯共聚物的球晶径向生长速率和形态[J].应用化学,1993,10(1):25-29. 被引量:3
  • 2[2]Gerhard M. Angew. Chem. Int. Ed., 1998, 37: 2960~2974.
  • 3[4]Bhide B D, Stern S A. J. Membr. Sci. , 1991, 62:13~35.
  • 4[5]Pandey P, Chauhan R S. Prog. Poly. Sci. , 2001, 26:853~893.
  • 5[6]Stern S A, J. Membr. Sci. , 1994, 94: 1~65.
  • 6[8]Alentiev A Y, Loza K A, Yampolskii Y P. J. Membr.Sci., 2000, 167: 91~106.
  • 7[9]Liu Y, Wang R, Chung T S. J. Membr. Sci. , 2001,189: 231~239.
  • 8[10]Lin W H , Chung T S. J. Membr. Sci. , 2001, 186:183~193.
  • 9[11]Masri M A, Kricheldorf H R, Fritsh D. Macromolecules., 1999, 32: 1853~1858.
  • 10[12]Fang J H, Kits H, Okamoto K. Macromolecules,2000, 33(13): 4639~4646.

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同被引文献20

  • 1汪国庆,姚兰芳,沈军,吴广明.聚对二甲苯防潮薄膜的研究[J].同济大学学报(自然科学版),2005,33(10):1337-1341. 被引量:10
  • 2李国民,李俊凤,刘静芝,吴庸烈.水蒸气在高分子膜中吸附和传递行为的研究进展[J].功能高分子学报,2005,18(4):696-702. 被引量:4
  • 3吉祥波,鲜晓斌,唐贤臣,帅茂兵,赵宗峰.热处理对Parylene C薄膜性能的影响[J].现代塑料加工应用,2007,19(4):9-11. 被引量:11
  • 4SEONWANG K, PARK J H, LEE J H, et al. Effect of At-mosphericplasma treatments for enhancing adhesion of Au on parylene C coated protein chips [ J ]. J Korean Phys Soc, 2004, 44 (5): 1168-1172.
  • 5KAHOULI A, SYLVESTRE A, PAIRIS S, et al. Effect of 02 x Ar/H2 and CF4plasmatreatments on the structural and di- electricproperties of parylene C thin films [ J ]. Appl Pbys, 2012, 45 (21): 1-7.
  • 6SEONGJW, KIMKW, BEAGYW, etal. Effects of ion bombardment withreactive gas environment on adhesion of Au films to parylene c film [ J ]. Thin Solid Films, 2005, 476 (2) : 386-390.
  • 7THOMPSON A, TREBICKY T, CREWDSON P, et al. Functional polymer laminates from hyperthermal hydrogen induced cross-linking [ J]. American Chem Soc, 2011, 27 (2): 14820-14827.
  • 8ZHENG Z, XU X D, FAN X L, et 81. Ultrathin polymer film formation by collisioninduced cross-linking of adsorbed organic molecules with hyperthermal protons [ J ]. J Am Chem, 2004, 126 (39): 12336-12342.
  • 9ZHENG Z, KWOK W M, LAU W M. A new cross-linking route via the unusual collision kinematics of hyperthermal protons in unsaturated hydrocarbons: the case of poly (trans-isoprene) [J]. Chem Communications, 2006, 29(3) : 3122-3124.
  • 10LAU W M, ZHENG Z, WANG Y H, et al. Cross-linking organic semiconducting molecules by preferential C-H cleav- age via "chemistry with a tiny hammer" [ J]. J Chem, 2007, 85 (10): 859-865.

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