化工进展
化工進展
화공진전
CHEMICAL INDUSTRY AND ENGINEERING PROGRESS
2015年
2期
376-380
,共5页
餐饮废油%生物柴油%碱木质素%活性炭%固体催化剂%酯交换反应
餐飲廢油%生物柴油%堿木質素%活性炭%固體催化劑%酯交換反應
찬음폐유%생물시유%감목질소%활성탄%고체최화제%지교환반응
waste cooking oil%biodiesel%Kraft lignin%activated carbon%solid catalyst%transesterification
以K2CO3为催化剂,工业碱木质素(KL)为活性炭(AC)前体,在管式电阻炉中经一步共混活化(K2CO3/KL质量比为0.6、活化温度800℃、N2流量100cm3/min、活化时间2h)制备K2CO3/AC固体碱催化剂,用于餐饮废油与甲醇的酯交换反应合成生物柴油。对制备的固体碱催化剂进行了 X-射线衍射(XRD)、BET 表面积及扫描电镜(SEM)表征。考察了反应温度、催化剂用量、反应时间、醇油摩尔比等因素对餐饮废油转化为生物柴油产率的影响。结果表明当反应时间2h、反应温度60℃、醇油摩尔比15∶1、催化剂为原料油质量的3.0%时,生物柴油最大产率为87.5%。考查了催化剂的循环利用效果,结果表明催化剂能循环利用3次,第3次利用时生物柴油的产率仍达到80.7%。
以K2CO3為催化劑,工業堿木質素(KL)為活性炭(AC)前體,在管式電阻爐中經一步共混活化(K2CO3/KL質量比為0.6、活化溫度800℃、N2流量100cm3/min、活化時間2h)製備K2CO3/AC固體堿催化劑,用于餐飲廢油與甲醇的酯交換反應閤成生物柴油。對製備的固體堿催化劑進行瞭 X-射線衍射(XRD)、BET 錶麵積及掃描電鏡(SEM)錶徵。攷察瞭反應溫度、催化劑用量、反應時間、醇油摩爾比等因素對餐飲廢油轉化為生物柴油產率的影響。結果錶明噹反應時間2h、反應溫度60℃、醇油摩爾比15∶1、催化劑為原料油質量的3.0%時,生物柴油最大產率為87.5%。攷查瞭催化劑的循環利用效果,結果錶明催化劑能循環利用3次,第3次利用時生物柴油的產率仍達到80.7%。
이K2CO3위최화제,공업감목질소(KL)위활성탄(AC)전체,재관식전조로중경일보공혼활화(K2CO3/KL질량비위0.6、활화온도800℃、N2류량100cm3/min、활화시간2h)제비K2CO3/AC고체감최화제,용우찬음폐유여갑순적지교환반응합성생물시유。대제비적고체감최화제진행료 X-사선연사(XRD)、BET 표면적급소묘전경(SEM)표정。고찰료반응온도、최화제용량、반응시간、순유마이비등인소대찬음폐유전화위생물시유산솔적영향。결과표명당반응시간2h、반응온도60℃、순유마이비15∶1、최화제위원료유질량적3.0%시,생물시유최대산솔위87.5%。고사료최화제적순배이용효과,결과표명최화제능순배이용3차,제3차이용시생물시유적산솔잉체도80.7%。
K2CO3 supported activated carbon (AC) as solid catalyst was prepared by directly mixing K2CO3 with technical Kraft Lignin (KL) with the mass ratio of 0.6 and subsequently activating at 800℃ for 2h under 100cm3/min of N2 flow rate in a tubular furnace. The obtained solid base catalyst was characterized by XRD,BET surface area and SEM. It was found that the catalyst possessed mesoporous structure with an average pore diameter of 10 nm and a good dispersion of K2CO3 on the surface of AC support. The prepared K2CO3/AC solid catalyst was used for the transesterification reaction of waste cooking oil (WCO) with methanol in batch reactor.The effects of various parameters,such as reaction temperature,amount of catalyst,reaction time,and molar ratio of methanol to WCO,on biodiesel yield were investigated. A maximum biodiesel yield of 87.5% was obtained under the optimal condition as reaction temperature of 60℃,catalyst amount of 3.0%, methanol to WCO molar ratio of 15∶1 and reaction time of 2h. The effect of repeated use of K2CO3/AC catalyst on biodiesel yield was tested. The results indicated that the catalytic activity remained 80.7% when the catalyst was employed for the third time.