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厦门大学材料学院导师介绍:余兆菊

厦门大学 免费考研网/2014-04-12

厦门大学材料学院导师介绍:余兆菊
2012-07-16


  姓名:余兆菊  
  性别:女
  职称:副教授  
  学院:材料学院
  研究方向:有机硅功能高分子、生物医用高分子以及耐高温陶瓷材料金属有机先驱体的设计、合成与性能研究
  教学领域:主讲本科生《高分子材料化学实验》和《基础化学实验二》课程,主讲硕士生、博士生学位课《高分子合成与分子设计》、工程硕士的《高分子性能表征与测试》及《功能高分子及其性能》课程。
  招生:可提供良好的学习与科研条件,每年拟招本科毕业生(毕业论文)2-3人,硕士研究生1-2人,欢迎硕-博连读生。
  联系电话: **
  电子信箱: zhaojuyu@xmu.edu.cn

  个人简介

  余兆菊,博士,副教授,硕士生导师。主持国家自然科学基金(青年基金)、“十一五”重点项目一级子课题、福建省自然科学基金以及航空科学基金。作为主要技术骨干参与了“十五”和 “十一五”重点项目、国家自然科学基金重点项目、国家自然科学基金面上项目、福建省陶瓷重大专项、福建省重大科技项目、福建省重点课题等多项省部级以上课题。主要研究方向包括有机硅功能高分子、生物医用高分子以及耐高温陶瓷材料有机先驱体的设计、合成与性能研究。 

  工作经历
  厦门大学副教授(2007- )
  厦门大学讲师(2004-2007)
 
  教育经历
  2001-2004,武汉大学高分子化学与物理专业理学博士
  1999-2001,武汉大学高分子化学与物理专业理学硕士
 
  科研成果

  学术专著与论文

  1.“Preparation of a liquid boron-modified polycarbosilane and its ceramic conversion to dense SiC ceramics”,Polymers for advanced technologies,DOI 10.1002/pat.1777.
  2.“Preparation of hyperbranched polycarbosilane precursor to SiC ceramics following an efficient room temperature cross-linking process.”Journal of Materials Science,2010,45,6151-6158.
  3.“Modification of a liquid polycarbosilane with 9-BBN as a high-ceramic-yield precursor for SiC.”Reactive & Functional Polymers,2010,70,334-339.
  4.“Preparation and characterization of cellulose and konjac glucomannan blend film from ionic liquid.”Journal of Polymer Science: Part B: Polymer Physics, 2009, 47, 1686-1694.
  5.“Synthesis and Properties of Liquid Polycarbosilanes with Hyperbranched Structures”,Journal of Applied Polymer Science,2009,113(3),1611-1618.
  6.“Effect of Curing and Pyrolysis Processing on the Ceramic Yield
of a Highly Branched Polycarbosilane”,Jounal of Materials Science,2009,44,721-725.
  7.“Synthesis, Characterization and Pyrolytic Conversion of a Novel Liquid Polycarbosilane”,Journal of the American Ceramic Society,2008,91(10),3298-3302.
  8.“Polymer-ceramic conversion of a highly branched liquid polycarbosilane for SiC-based ceramics”,Journal of Materials Science, 2008, 43, 2806-2811.
  9.“Effect of the polycarbosilane structure on its final ceramic yield”, Journal of the European Ceramic Society, 2008, 28, 887-891.
  10.“One-pot synthesis and characterization of a new, branched polycarbosilane bearing allyl groups”, Chinese Chemical Letters, 2007, 18 (6), 754-757.
  11.“Microwave synthesis of poly (vinyl alcohol)–graft -poly(ε-caprolactone) copolymers”, Polymer Prepint,2007, 48 (1), 451-452.
  12.“Microwave synthesis of star-shaped poly(ε-caprolactone) with polyol initiator”, Abstracts of Papers of American Chemical Society, 2007, 233,PMSE-372.
  13.“Microwave-assisted synthesis of poly(ε-caprolactone)-poly(ethylene glycol)-poly(ε-caprolactone) tri-block co-polymers and use as matrices for sustained delivery of ibuprofen taken as model drug”,Journal of Biomaterials Science Polymer Edition, 2005, 16 (8), 957-971.
  14.“Effect of microwave energy on chain propagation of poly(ε-caprolactone) in benzoic acid-initiated ring opening polymerization of ε-caprolactone”,European Polymer Journal, 2004, 40 (9), 2213-2220.
  15.“Dye-molecular- imprinted polysiloxanes. II. Preparation, characterization and recognition behavior”, Journal of Applied Polymer Science, 2004, 93(2), 637-643.
  16.“Microwave synthesis of PCL/PEG/PCL triblock copolymers and drug release system thereof”, Transactions - 7th World Biomaterials Congress, 2004, 672.
  17.“Microwave-improved polymerization of ε-caprolactone initiated by carboxylic acids”,Journal of Polymer Science Part A: Polymer chemistry, 2003, 41, 13-21.
  18.“Microwave irradiation effect on the polymerization of ε-caprolactone with benzoic acid as initiator”,Polym. Prepr., 2003, 44(1), 868-869.
  19.“Microwave-assisted synthesis of poly(ε-caprolactone) with acid as initiator and a novel method in preparation drug release systems”, Polym. Prepr., 2003, 44(1), 936-937.
  20. “偶氮二异丁腈引发液态聚碳硅烷的交联研究”,硅酸盐学报,2009,37(8), 105-109。
  21. “过氧化苯甲酰在液态聚碳硅烷交联中的应用”,功能材料,2009,40,2058-2060。
  22.“液态超支化聚碳硅烷的研究进展”,功能材料,2010,41,1113-1116。
  23.“低氧含量液态超支化聚碳硅烷的合成与陶瓷化研究”,功能材料,2010,在印中。
  24.国家发明专利,ZL-02-1-15944.0。
  25.国防发明专利,**5.7。
  26.国防发明专利,**7.0。
  27.国防发明专利,**3.5
  28.国防发明专利,**4.9
  29.国防发明专利,**3.4



   

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