生物质化学工程
生物質化學工程
생물질화학공정
Biomass Chemical Engineering
2015年
6期
1-5
,共5页
张传伟%李方义%刘鹏%王成钊%李剑峰%郭安福
張傳偉%李方義%劉鵬%王成釗%李劍峰%郭安福
장전위%리방의%류붕%왕성쇠%리검봉%곽안복
剑麻纤维%热塑性淀粉复合材料%热稳定性%微观形貌
劍痳纖維%熱塑性澱粉複閤材料%熱穩定性%微觀形貌
검마섬유%열소성정분복합재료%열은정성%미관형모
sisal fiber%thermoplastic starch composites%thermal stability%micro-morphology
为研究剑麻纤维增强的热塑性淀粉复合材料的制备工艺及热稳定性,以玉米淀粉为原料,先制得热塑性淀粉,再以剑麻纤维为骨架增强体制备剑麻纤维增强热塑性淀粉复合材料,通过正交试验优化制备工艺,DSC、TG/DTG、SEM分析其热稳定性及结构。正交试验表明,各因素对材料抗拉强度影响的主次顺序为纤维长度>纤维用量>模压成型温度>填料用量;最佳工艺条件为纤维长度15 mm、纤维用量35 g、模压成型温度200℃、填料用量5 g,此时材料的抗拉强度可达到4.45 MPa。利用差示扫描量热分析和热重分析分别对热塑性淀粉及剑麻纤维复合材料的热稳定性进行了分析,结果表明,热塑处理提高了淀粉的熔融温度,有利于淀粉与纤维素羟基间的氢键结合,且热塑过程在一定程度上降低了淀粉的热稳定性;剑麻纤维复合材料的热降解过程主要发生在200~400℃温度区间。 SEM分析显示最佳工艺条件下得到的复合材料具有较好的泡孔结构。
為研究劍痳纖維增彊的熱塑性澱粉複閤材料的製備工藝及熱穩定性,以玉米澱粉為原料,先製得熱塑性澱粉,再以劍痳纖維為骨架增彊體製備劍痳纖維增彊熱塑性澱粉複閤材料,通過正交試驗優化製備工藝,DSC、TG/DTG、SEM分析其熱穩定性及結構。正交試驗錶明,各因素對材料抗拉彊度影響的主次順序為纖維長度>纖維用量>模壓成型溫度>填料用量;最佳工藝條件為纖維長度15 mm、纖維用量35 g、模壓成型溫度200℃、填料用量5 g,此時材料的抗拉彊度可達到4.45 MPa。利用差示掃描量熱分析和熱重分析分彆對熱塑性澱粉及劍痳纖維複閤材料的熱穩定性進行瞭分析,結果錶明,熱塑處理提高瞭澱粉的鎔融溫度,有利于澱粉與纖維素羥基間的氫鍵結閤,且熱塑過程在一定程度上降低瞭澱粉的熱穩定性;劍痳纖維複閤材料的熱降解過程主要髮生在200~400℃溫度區間。 SEM分析顯示最佳工藝條件下得到的複閤材料具有較好的泡孔結構。
위연구검마섬유증강적열소성정분복합재료적제비공예급열은정성,이옥미정분위원료,선제득열소성정분,재이검마섬유위골가증강체제비검마섬유증강열소성정분복합재료,통과정교시험우화제비공예,DSC、TG/DTG、SEM분석기열은정성급결구。정교시험표명,각인소대재료항랍강도영향적주차순서위섬유장도>섬유용량>모압성형온도>전료용량;최가공예조건위섬유장도15 mm、섬유용량35 g、모압성형온도200℃、전료용량5 g,차시재료적항랍강도가체도4.45 MPa。이용차시소묘량열분석화열중분석분별대열소성정분급검마섬유복합재료적열은정성진행료분석,결과표명,열소처리제고료정분적용융온도,유리우정분여섬유소간기간적경건결합,차열소과정재일정정도상강저료정분적열은정성;검마섬유복합재료적열강해과정주요발생재200~400℃온도구간。 SEM분석현시최가공예조건하득도적복합재료구유교호적포공결구。
In order to further research composition process and the thermal stability of thermoplastic starch composites reinforced with plant fiber, the composites were prepared by reinforcing the thermoplastic starch obtained from corn starch with sisal fiber as skeleton reinforcing agent. The orthogonal test was designed to optimize the preparation process. DSC, TG/DTG and SEM were used to analyze the thermal stability and the structure of the composites. The results showed that the order of the influences of various factors on the tensile strength of the material was fiber length>fiber content>molding temperature>filler content. And the tensile strength of the material was 4. 45 MPa, when the fiber length was 15 mm, the fiber content was 35 g, the molding temperature was 200℃ and the filler content was 5 g. The thermal stabilities of thermoplastic starch and sisal fiber composite were analyzed. The results showed that the thermoplastic treatment could increase the melting temperature of starch, benefit for the hydrogen-bonding between starch and the hydroxy of cellulose, and decrease the thermal stability of starch. The thermal degradation process of sisal fiber composites mainly occured in the temperature range 200-400℃. SEM images showed that the composites possessed great foam structure under the optimistic process conditions.