CHINESE JOURNAL OF ENERGETIC MATERIALS
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炔丙基二甲基海因改性GAP的合成及应用
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Synthesis of PDMH-GAP and Its Application
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    摘要:

    3-炔丙基-5,5-二甲基海因(PDMH)与聚叠氮缩水甘油醚(GAP)在二甲基甲酰胺(DMF)溶剂中进行反应,反应摩尔比为: PDMH/GAP=6/7,反应在60 ℃的条件下进行48 h反应完全。PDMH上的炔基与GAP上的叠氮基团发生反应,反应产物为GAP-PDMH。对GAP-PDMH进行了傅立叶变换红外光谱和核磁共振氢谱分析,测定了GAP-PDMH的玻璃化转变温度。实验结果表明,PDMH通过1,3-偶极环加成反应生成三唑五元环结构进入到叠氮粘合剂的侧链中。把GAP-PDMH应用到GAP推进剂的配方中,进行了力学性能测试。与空白样相比较,GAP-PDMH的加入使得推进剂的常温抗拉强度提高了210%,达到了0.65 MPa; 最大延伸率提高了226%,达到了22.24%; 断裂延伸率提高了207%,达到了25.87%。

    Abstract:

    GAP-PDMH was prepared by the chemical reaction between alkyne and azide in DMF,and the molar ratio was 6/7. The reaction temperature was 60 ℃ and reaction time was 48 h. The GAP-PDMH was identified by FT-IR and 1H NMR, and glass transition temperature of the GAP-PDMH was measured. Results show that PDMH is grafted into the branch of GAP chains by 1, 3-dipolar cycloaddition reaction between alkyne and azide. Mechanical properties of composite GAP propellant with GAP-PDMH were tested. Compared with the blank sample, GAP-PDMH can improve the mechanical properties of the composite propellant at room temperature. The maximum tensile strength is increased by 210% (to be 0.65 MPa); the maximum elongation is increased by 226% (to be 22.24%); the fracture elongation is increased by 207% (to be 25.87%).

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引用本文

张丽娜,杨荣杰.炔丙基二甲基海因改性GAP的合成及应用[J].含能材料, 2009, 17(5):514-517. DOI:10.3969/j. issn.1006-9941.2009.05.004.
ZHANG Li-na, YANG Rong-jie. Synthesis of PDMH-GAP and Its Application[J]. Chinese Journal of Energetic Materials, 2009, 17(5):514-517. DOI:10.3969/j. issn.1006-9941.2009.05.004.

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  • 收稿日期: 2009-02-05
  • 最后修改日期: 2009-07-26
  • 录用日期: 2009-04-01
  • 在线发布日期: 2009-10-15
  • 出版日期: 2009-10-25