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Synthesis and Properties of Thermosetting Modified Polyphenylene Ether

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Summary

A novel method for preparing thermosetting modified Poly(2,6-dimethyl-1,4-phenylene ether) (PPE) was developed by introducing allyl groups into PPE. It was successfully prepared from the reaction between brominated PPE and a Grignand reagent. The effects of substitution of bromine on methyl group and dosage of allylated Grignard reagent on the substitution value of allyl group were studied. The structure of the resulting allylated PPE (A-PPE) was characterized by 1H-NMR and FT-IR spectroscopy. The curing reaction process was researched by differential scanning calorimetry (DSC), and the properties of the cured A-PPE were also investigated. The curing reaction of the A-PPE was first order reaction. The curing reaction activation energy obtained by Kissinger equation was 121.7 kJ/mol. The cured A-PPE resin is excellent not only in solvent resistance and dielectric properties, but also in thermal properties, moisture absorption and adhesion with glass fiber. The dielectric constant (ε) and dissipation factor (tan δ) of A-PPE composites reinforced with E-glass cloth at 1 MHz were measured as 2.84 and 2.65×10-3, respectively. In addition, A-PPE was very easy to form into films.

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References

  1. Gang H, Lining Y, Hongxin C (1999) Appl Eng Plastics 27(12):19

    Google Scholar 

  2. Ishii Y, Oda H, Arai T, Katayose T (1995) Polym Mater Sci Eng 72:448

    Google Scholar 

  3. Toshiaki F, Yuji S, Shinji A, Mitsuru U (2004) Polymer 45:843

    Google Scholar 

  4. Silvia GP, Cabanelas JC (2004) J Appl Polym Sci 93:2678

    Google Scholar 

  5. Herbert SC, Jana MW (1996) J Appl Polym Sci 59:473

    Google Scholar 

  6. Yoshiyuki I, Anthony JR, Nigel C (2003) Polymer 44:3641

    Google Scholar 

  7. Girard-Reydet E, Sautereau H, Pascault JP (1999) Polymer 40:1677

    Google Scholar 

  8. Venderbosch RW, Peijst T, Meijer HEH (1996) Composites Part A 27A:895

  9. Wu SJ, Tung NP, Lin TK, Shyu SS (2000) Polym Int 49:1452

  10. Wu SJ, Lin TK, Shyu SS (2000) J Appl Polym Sci 75:26

    Google Scholar 

  11. James ET, Gary WY (2000) US Patent 6051662

  12. Teruo KS, Yoshiyuki IY (1994) US Patent 5352745

  13. Harry LF, Yao HH (1989) Macromolecules 22:91

    Google Scholar 

  14. Jiru M, Guozheng L, Lei Z (2002) Comp Sci Techno 62:783

    Google Scholar 

  15. Teruo K, Hiroji O, Haruhisa S (1993) US Patent 5218030

  16. Katayose et al. (1990) US Patent 4923932

  17. Juraj L, Eberhard B, Ivan T (1993) Die Angewandte Makromolekulare Chemie 211:121

    Google Scholar 

  18. van den A TR, Steven H (1995) J Organometal Chem 502:35

  19. Ehlers AW, Van Klink GPM (2000) J Mole Model 6(2):186

    Google Scholar 

  20. Brandolim A (2000) NMR spectra of polymer and polymer additives. New York:Marcel Dekker

  21. Jianqiang H, Lianda J, Jiping X (1989) J Funct Polymers 2(2):121

    Google Scholar 

  22. Kissinger H E (1957) Anal Chem 29(11):1702–1706

    Google Scholar 

  23. Yaoxian Wang, Shujun Cheng, Chongyuan Shen, Fan Li (2003) J East China University Sci Technol 29(3):273–276

  24. Jindu L (2003) Printed Circuit Information (7):3

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Correspondence to Yaoxian Wang.

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Wang, Y., Cheng, S., Li, W. et al. Synthesis and Properties of Thermosetting Modified Polyphenylene Ether. Polym. Bull. 59, 391–402 (2007). https://doi.org/10.1007/s00289-007-0775-8

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  • DOI: https://doi.org/10.1007/s00289-007-0775-8

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