摘要
为改善含能粘结剂及增塑剂的流变性与氧平衡,用聚环氧氯丙烷(PECH)、叠氮钠(NaN3)、氢氧化钠(NaOH)、在乙二醇(EG)引发下,100℃反应获得了支化聚叠氮缩水甘油醚(B-GAP),浓硝酸-20~0℃反应,将B-GAP转化为支化聚叠氮缩水甘油醚硝酸酯(B-GAPN)。研究了用反应条件控制B-GAP羟值及B-GAP与B-GAPN分子量。从B-GAP红外光谱的-OH特征峰削弱和-ONO2峰的出现,可判断合成产物为B-GAPN。
Branched glycidyl azide polymer ( B-GAP ) was obtained at 100 ℃, using poly epoxy chloropropane, sodium azide, and sodium hydroxide as reactants and glycol as initiator. B-GAP was transformed to branched glycidyl azide polymer nitrate ( B-GAPN ) with concentrated nitric acid at -20 -0℃. Reaction parameters were used to controll molecular weight and hydroxy number of B- GAP,and moeeular weight of B-GAPN. The preparation product B-GAPN is testified by infrared spectrum analysis which indicates evident decrease of hydroxy group and emergence of nitrate peak.
出处
《含能材料》
EI
CAS
CSCD
2008年第4期395-397,共3页
Chinese Journal of Energetic Materials
基金
中国工程物理研究院基金(No.960574)