功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
18期
18058-18062
,共5页
周海骏%张玉%张婷婷%郭伟杰%张娇霞
週海駿%張玉%張婷婷%郭偉傑%張嬌霞
주해준%장옥%장정정%곽위걸%장교하
原位聚合%环状对苯二甲酸丁二醇酯%聚环状对苯二甲酸丁二醇酯%复合材料
原位聚閤%環狀對苯二甲痠丁二醇酯%聚環狀對苯二甲痠丁二醇酯%複閤材料
원위취합%배상대분이갑산정이순지%취배상대분이갑산정이순지%복합재료
in-situ polymerization%cyclic butylene terephthalate%poly(cyclic butylene terephthalate)%composites
采用环状对苯二甲酸丁二醇酯(CBT)原位聚合制备了玻璃纤维(GF)增强聚环状对苯二甲酸丁二醇酯(PCBT)复合材料。研究了聚合温度及催化剂用量对 PCBT 粘均分子量、结晶度以及 GF/PCBT 复合材料力学性能的影响。结果表明,随着聚合温度的升高,PCBT的粘均分子量及结晶度逐渐增大并趋于稳定,GF/PCBT复合材料力学性能也不断增大;当聚合温度为210℃时,PCBT 的粘均分子量为7.16×104 g/mol,结晶度为43.9%,GF/PCBT 复合材料的拉伸和弯曲强度分别为(271.44±3.40)和(257.70±3.73)MPa。随着催化剂用量的增大,PCBT的粘均分子量和结晶度逐渐增大并趋于稳定,复合材料力学性能不断增强;当催化剂用量为0.4%(质量分数)时, PCBT的粘均分子量为7.13×104 g/mol,结晶度为44.4%,GF/PCBT 复合材料的拉伸和弯曲强度分别为(265.10±3.31)和(260.30±2.03)MPa。
採用環狀對苯二甲痠丁二醇酯(CBT)原位聚閤製備瞭玻璃纖維(GF)增彊聚環狀對苯二甲痠丁二醇酯(PCBT)複閤材料。研究瞭聚閤溫度及催化劑用量對 PCBT 粘均分子量、結晶度以及 GF/PCBT 複閤材料力學性能的影響。結果錶明,隨著聚閤溫度的升高,PCBT的粘均分子量及結晶度逐漸增大併趨于穩定,GF/PCBT複閤材料力學性能也不斷增大;噹聚閤溫度為210℃時,PCBT 的粘均分子量為7.16×104 g/mol,結晶度為43.9%,GF/PCBT 複閤材料的拉伸和彎麯彊度分彆為(271.44±3.40)和(257.70±3.73)MPa。隨著催化劑用量的增大,PCBT的粘均分子量和結晶度逐漸增大併趨于穩定,複閤材料力學性能不斷增彊;噹催化劑用量為0.4%(質量分數)時, PCBT的粘均分子量為7.13×104 g/mol,結晶度為44.4%,GF/PCBT 複閤材料的拉伸和彎麯彊度分彆為(265.10±3.31)和(260.30±2.03)MPa。
채용배상대분이갑산정이순지(CBT)원위취합제비료파리섬유(GF)증강취배상대분이갑산정이순지(PCBT)복합재료。연구료취합온도급최화제용량대 PCBT 점균분자량、결정도이급 GF/PCBT 복합재료역학성능적영향。결과표명,수착취합온도적승고,PCBT적점균분자량급결정도축점증대병추우은정,GF/PCBT복합재료역학성능야불단증대;당취합온도위210℃시,PCBT 적점균분자량위7.16×104 g/mol,결정도위43.9%,GF/PCBT 복합재료적랍신화만곡강도분별위(271.44±3.40)화(257.70±3.73)MPa。수착최화제용량적증대,PCBT적점균분자량화결정도축점증대병추우은정,복합재료역학성능불단증강;당최화제용량위0.4%(질량분수)시, PCBT적점균분자량위7.13×104 g/mol,결정도위44.4%,GF/PCBT 복합재료적랍신화만곡강도분별위(265.10±3.31)화(260.30±2.03)MPa。
Glass fiber(GF)reinforced poly(cyclic butylene terephthalate)(PCBT)composites were prepared by in-situ polymerization of cyclic butylene terephthalate(CBT).The effects of the polymerization temperature and the catalyst content on the viscosity average molecular weight,the crystallinity of PCBT and the mechanical properties of GF/PCBT composites were investigated.The experimental results indicated that the viscosity-av-erage molecular weight and the crystallinity of PCBT were gradually increased and finally tended to stabilization with increasing of polymerization temperature.The mechanical properties of the GF/PCBT composites were constantly strengthened with increasing of polymerization temperature.When the polymerization temperature was 210 ℃,the viscosity-average molecular weight of PCBT was 7.16×104 g/mol,and its crystallinity reached 43.9%,the tensile strength and flexural strength of the GF/PCBT composites was (271.44 ± 3.40)and (257.70±3.73)MPa,respectively.With increasing of catalyst mass fraction,the viscosity-average molecular weight and the crystallinity of PCBT were gradually increased and finally tended to stabilization.The mechani-cal properties of the GF/PCBT composites were constantly strengthened with increasing of catalyst mass frac-tion.When the catalyst mass fraction reached 0.4wt%,the viscosity-average molecular weight of PCBT was 7.13×104 g/mol,and its crystallinity reached 44.4%,the tensile strength and flexural strength of the GF/PCBT composites was (265.10±3.31)and (260.30±2.03)MPa,respectively.