期刊文献+

冰片烯-二氧化硫聚砜树脂的合成及表征(英文) 被引量:1

Synthesis and Characterization of Bornylene-sulfur Dioxide Polysulfone Resin
下载PDF
导出
摘要 以α-蒎烯为原料合成冰片烯。以冰片烯(BE)、二氧化硫(SO2)为单体,采用自由基聚合方法合成了冰片烯-二氧化硫聚砜树脂(BE-SO2),用同样的方法分别以冰片烯(BE)、二氧化硫(SO2)、马来酸酐为单体和以冰片烯(BE)、二氧化硫(SO2)、苯乙烯(St)为单体,合成冰片烯-二氧化硫-马来酸酐(BE-SO2-M a)以及冰片烯-二氧化硫-苯乙烯(BE-SO2-St)两种三元共聚物。讨论了单体配比、聚合反应的温度和时间对共聚物得率的影响,结果表明:n(BE)1 mmol,n(BE)∶n(M a)1∶1,n(BE)∶n(St)1∶1,加入4 mL CYC作溶剂,在-20℃条件下反应4 h,BE-SO2,BE-SO2-M a,BE-SO2-St得率最高,分别为70%、64%和71%。此外,分别用FT-IR、GPC、DSC、EA和SEM等方法对共聚物结构进行了表征,BE-SO2为粉末状黑色固体,重均相对分子质量(Mw)为1 069,数均相对分子质量(Mn)为376,Tg为134.5℃;BE-SO2-M a共聚物为粉末状黑褐色固体,Mw为1 576,Mn为402,Tg为152.0℃;BE-SO2-St共聚物为粉末状黄褐色固体,Mw为33 054,Mn为952,Tg为174.8℃。 Bornylene-sulfurdioxide polysulfone resin(BE-SO2)was synthesized by free radical copolymerization of monomers SO2 and bornylene(BE) which synthesized from α-pinene.Similarly,BE-SO2-Ma and BE-SO2-St were synthesized using BE,SO2,maleic anhydride(MA) as monomers and BE,SO2,styrene(St) as monomers respectively.Effects of operating conditions such as monomer ratio,polymerization temperature and reaction time on the copolymer yields are discussed.The results showed that the optimum reaction conditions are as follows: reaction temperature-20℃,reaction time 4 h,n(BE)1mmol,n(BE)∶n(Ma)1∶1,n(BE)∶n(St)1∶1,CYC as solvent and volume 4 mL,and the highest yield of BE-SO2,BE-SO2-Ma,BE-SO2-St are 70%、64% and 71%,respectively.The structure of the copolymers were characterized by FT-IR,GPC,DSC,EA and SEM.BE-SO2 was a black solid powder with weight average molecular weight(Mw) of 1069,number average molecular weight(Mn) of 376,and Tg of 134.5℃;BE-SO2-Ma polysulfone resin is a dark brown solid powder with Mw of 1576,Mn of 402 and Tg of 152.0℃;BE-SO2-St polysulfone resin is a tan solid powder with MW of 33054,Mn of 952 and Tg of 174.8℃.
出处 《林产化学与工业》 EI CAS CSCD 北大核心 2011年第3期89-93,共5页 Chemistry and Industry of Forest Products
基金 国家自然科学基金资助项目(30771686)
关键词 冰片烯 二氧化硫 自由基聚合 聚砜树脂 bornylene sulfur dioxide free radical polymerization polysulfone resin
  • 相关文献

参考文献9

  • 1MASAHIRO Y. Industrialization and application development of cyclo-olefin polymer [ J ]. Journal of Molecular Catalysis A : Chemical, 2004, 213:81-87.
  • 2HSIN H Y, HWANG S J, TSENG M C, et al. The effect of ITO films thickness on the properties of flexible organic light emitting diode [ J ]. Optics Communications ,2006,259 : 187-193.
  • 3TORMQVIST E G M. Preparation of aluminoxane for olefin polymerization catalyst:US, EP208 561 [ P]. 1987.
  • 4赵振东,刘先章.松节油的精细化学利用(Ⅷ)——国内外现状及发展动向[J].林产化工通讯,2002,36(2):37-42. 被引量:14
  • 5林业部林产工业公司松香 松节油再加工产品市场调查组.松香松节油再加工市场调查报告.林产化工通讯,1990,:5-11.
  • 6BERGSTROM C, MOLSA A. Process for preparing cyclic monomers by the hydrochlorination of terpenes followed by their E2-eliminative de- hydrochlorination : WO,940050 [ P ]. 1999.
  • 7程健,冯涛,李开婧,曾韬.冰片烯的合成研究[J].林产化学与工业,2009,29(2):54-58. 被引量:10
  • 8程健.冰片烯及其聚合物的合成研究[D].南京:南京林业大学硕士学位论文,2008.
  • 9冯涛.冰片烯聚合物的制备研究[D].南京:南京林业大学硕士学位论文,2009.

二级参考文献12

  • 1余定学,戴自钦,李丽萍,余晓华,谢金伦.刺柏叶精油的化学成分研究[J].云南大学学报(自然科学版),1994,16(2):145-148. 被引量:8
  • 2刘布鸣,赖茂祥,蔡全玲,彭维,郑学忠.马山前胡挥发油化学成分研究[J].分析化学,1995,23(8):885-888. 被引量:6
  • 3吴仲国.2001年诺贝尔化学奖得主野依良治[J].科技日报,2001,10.
  • 4黄志喜 王慧辰.萜类香料化学[M].北京:中国轻工业出版社,1999..
  • 5BERGSTROM C, MOLSA A. Process for preparing cyclic monomers by the hydrochlorination of terpenes followed by their E2-eliminative dehydrochlorination : WO ,9940050 [ P]. 1999.
  • 6JAMES W, FEAST V C, GIBSON K J. Metathesis polymerization of 1,7,7-trimethyl bicyclo [ 2.2. 1 ] hept-2-ene using a well defined molybdenum initiator [ J ]. Journal of Molecular Catalysis, 1994,90:87-99.
  • 7LONG J H. On the optical rotation of pinene hydrochloride [ J ]. Journal of American Chemical Society, 1989,21 ( 8 ) :637-642.
  • 8WINSTEIN S, ETSYK B, GRUNWALDH M, et al. Neighboring carbon and hydrogen (VII). Reactivity of some alicyclic and bicyclicderivative [ J]. Journal of American Chemical Society, 1952,74 : 1127-1132.
  • 9BOROWIECK L, CHRETIEN-BESSIERE Y. ETUDE du bornylene[ J]. Bull Soc Chim Fr, 1967,23:64.
  • 10ROBERT H, SHAPIRO D J H. 2-Bornene [ 1,7,7-trimethyl-bicyclo [ 2.2.1 ] hept-2-ene ] [ J ]. Organic Syntheses Coll, 1988 (6) : 172.

共引文献22

同被引文献39

  • 1Alexander R J,Doyle J R.Polysulfones of norbomadiene[J].J.Polym.Sci.Part B:Polym.Lett.,1963,1:625-627.
  • 2Matsuda M,Hara Y.Radical copolymerization of sulfur dioxide and chloroprene[J].J.Polym.Sci.Part A-1:Polym.Chem.,1972,10:837-843.
  • 3Schaefer J.Equilibrium of catalytic states in the copolymerization of propylene oxide and sulfur dioxide[J].Macromolecules,1968,1:111-116.
  • 4Soga K,Kiyohara K,Hattori I,et al.Alternating copolymerization of cyclohexene oxide and sulfur dioxide[J].Die Makromol.Chem.,1980,181:2151-2159.
  • 5Seyer W F,King E G.Systems of sulfur dioxide and hydrogen derivatives of benzene[J].J.Am.Chem.Soc.,1933,55:3140-3149.
  • 6Frederick DS,Cogan HD,Marvel C S.The reaction between sulfur dioxide and olefins cyclohexene[J].J.Am.Chem.Soc.,1934,56:18154819.
  • 7Zutty N L,Wilson C W,Potter G H,et al.Copolymerization studies.VI.Spontaneous copolymerization of bicyclo[2.2.1].hept-2-cne and sulfur dioxide.Evidence for propagation by biradical coupling[J].J.Polym.Sci.Part A:Gen.Pap,,1965,3:2781-2799.
  • 8Amemiya Y,Katayama M,Harada S.The cyclo-copoljnnerization of diallyl ccanpounds and sulfur dioxide,4.4-(4-pyridyl)1,6 heptadiene hydrochloride and sulfur dioxide[J].Die Makromol.Chem.,1975,176;1289-1305,.
  • 9Harada S,Arai K.The cyclo-copolymerization of diallyl compounds and sulfur dioxide.III.Some diallylamine derivatives and sulfur dioxide[J].Di Die Makramol.Chem.,1967,107:78-93.
  • 10Harada S,Katayama M.Thecyclocopolymerizatiotiofdiallyl compound and sulfur dioxide.I.Diallylamine hydrochloride and sulfur dioxide[J].Die Makromol.Chem.,1966,90:177-186.

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部