高分子学报
高分子學報
고분자학보
ACTA POLYMERICA SINICA
2001年
1期
84-89
,共6页
李鑫%李瑞霞%吴大诚%孙琳%宋青%国凤敏%吴立衡
李鑫%李瑞霞%吳大誠%孫琳%宋青%國鳳敏%吳立衡
리흠%리서하%오대성%손림%송청%국봉민%오립형
PET%收缩%表征
PET%收縮%錶徵
PET%수축%표정
采用广角X-射线衍射、密度梯度、声速和差示扫描量热等实验方法对1455dtex/110f成品涤纶工业丝等温收缩的结构变化进行了表征,外加张力为0.3N,测定温度范围375~494K.结果表明,涤纶工业丝的热收缩在宏观上表现为速率不同的两个过程,对应两种不同机理.其中快过程对应非晶区的解取向,对收缩的贡献是主要的;慢过程对应晶区的变化,包含了晶粒的增长,新的不完善晶粒的形成和晶区的完善.晶粒的增长在较短的时间内基本完成,再结晶则存在于整个收缩过程.随温度的升高,晶区变化速度明显加快,对非晶区解取向的抑制效应因此变大.
採用廣角X-射線衍射、密度梯度、聲速和差示掃描量熱等實驗方法對1455dtex/110f成品滌綸工業絲等溫收縮的結構變化進行瞭錶徵,外加張力為0.3N,測定溫度範圍375~494K.結果錶明,滌綸工業絲的熱收縮在宏觀上錶現為速率不同的兩箇過程,對應兩種不同機理.其中快過程對應非晶區的解取嚮,對收縮的貢獻是主要的;慢過程對應晶區的變化,包含瞭晶粒的增長,新的不完善晶粒的形成和晶區的完善.晶粒的增長在較短的時間內基本完成,再結晶則存在于整箇收縮過程.隨溫度的升高,晶區變化速度明顯加快,對非晶區解取嚮的抑製效應因此變大.
채용엄각X-사선연사、밀도제도、성속화차시소묘량열등실험방법대1455dtex/110f성품조륜공업사등온수축적결구변화진행료표정,외가장력위0.3N,측정온도범위375~494K.결과표명,조륜공업사적열수축재굉관상표현위속솔불동적량개과정,대응량충불동궤리.기중쾌과정대응비정구적해취향,대수축적공헌시주요적;만과정대응정구적변화,포함료정립적증장,신적불완선정립적형성화정구적완선.정립적증장재교단적시간내기본완성,재결정칙존재우정개수축과정.수온도적승고,정구변화속도명현가쾌,대비정구해취향적억제효응인차변대.
The structure changes of the industrial yarn of poly(ethylene terephthalate)(PET)of 1455dTex/110f under the tension of 0\^3N and at the temperature range of 375~494K were characterized by WAXD, density gradient method, sonic velocity measurements,and DSC.The shrinkage could be divided into two different processes characterized by different relaxation times and final shrinkage amounts.The molecular mechanism for the first process, the fast and dominant one, mainly was the disorientation of the extended segments in the amorphous region, which can be proved by the change of orientation function of the amorphous region(fam)with shrinkage time at different temperatures. More meaningful thing is that the shape and change tendencies of fam and relative length (lt) with shrinkage time are very similar. The second slow one was resulted from the restructuring of the crystalline region, which included the rapid growth of the crystallites, the formation of new imperfect crystals and the reorganization of existed crystals during the whole shriknage process. The changes of crystalline regions became fast with the temperature rising and consequently their effect of restriction of the disorientation of the amorphous region became more obvious. However, the orientation function of crystalline regions keeps unchanged almost during the thermal shrinkage process. It should be indicated that the structure changes of amorphous and crystalline regions are not independently. Each process proceeds and competes each other during the thermal shriknage.The contribution of both processes to the shrinkage mainly depends on the temperature and time.The study of structure change of PET yarn during thermal shrinkage provides an important idea of developing more perfect crystalline regions to limit the thermal shrinkage due to the disorientation in amorphous regions.PET yarns with strength of 7cN/dTex,modulus of 4\^4cN/dTex at 5% elongation and thermal shrinkage of 3\^5% have been successfully obtained.