生物质化学工程
生物質化學工程
생물질화학공정
BIOMASS CHEMICAL ENGINEERING
2015年
2期
1-6
,共6页
罗华超%陈禾木%陈颖超%封卫%王琛%秦必达%任世学
囉華超%陳禾木%陳穎超%封衛%王琛%秦必達%任世學
라화초%진화목%진영초%봉위%왕침%진필체%임세학
改性碱木质素%聚乙烯醇%发泡材料
改性堿木質素%聚乙烯醇%髮泡材料
개성감목질소%취을희순%발포재료
modified alkali lignin%polyvinyl alcohol%foaming material
以改性碱木质素与聚乙烯醇( PVA)为原料,甲醛为交联剂,采用无机发泡原理,制备了聚乙烯醇/碱木质素发泡材料( PLFM)、聚乙烯醇/环氧化碱木质素发泡材料( PELFM)和聚乙烯醇/羟甲基化碱木质素发泡材料( PHLFM),并利用红外光谱、扫描电镜、DSC及TG对发泡材料进行了测定及分析。结果表明, PVA用量为5 g时,环氧化碱木质素用量为50%(以 PVA 质量计,下同),甲醛用量24%,硫酸用量54%,固化温度120℃制备的 PELFM 拉伸强度最大,为17.26 MPa。 FT-IR分析显示, PLFM和PHLFM的苯环5位均发生取代,而PELFM没有发生取代;SEM图片显示发泡材料的孔径不规则,孔隙率较大;与另两种发泡材料相比,PELFM拉伸性能低,表观密度较低,吸水倍率也较低。从DSC和TG分析可知,3种发泡材料中PELFM具有较低的玻璃态转变温度,但其生物相容性最好,PELFM失重率最高峰对应的峰值温度最大且介于碱木质素与PVA之间,烧失后残余量也最大,表明PELFM的耐热性更好,热稳定性更强。
以改性堿木質素與聚乙烯醇( PVA)為原料,甲醛為交聯劑,採用無機髮泡原理,製備瞭聚乙烯醇/堿木質素髮泡材料( PLFM)、聚乙烯醇/環氧化堿木質素髮泡材料( PELFM)和聚乙烯醇/羥甲基化堿木質素髮泡材料( PHLFM),併利用紅外光譜、掃描電鏡、DSC及TG對髮泡材料進行瞭測定及分析。結果錶明, PVA用量為5 g時,環氧化堿木質素用量為50%(以 PVA 質量計,下同),甲醛用量24%,硫痠用量54%,固化溫度120℃製備的 PELFM 拉伸彊度最大,為17.26 MPa。 FT-IR分析顯示, PLFM和PHLFM的苯環5位均髮生取代,而PELFM沒有髮生取代;SEM圖片顯示髮泡材料的孔徑不規則,孔隙率較大;與另兩種髮泡材料相比,PELFM拉伸性能低,錶觀密度較低,吸水倍率也較低。從DSC和TG分析可知,3種髮泡材料中PELFM具有較低的玻璃態轉變溫度,但其生物相容性最好,PELFM失重率最高峰對應的峰值溫度最大且介于堿木質素與PVA之間,燒失後殘餘量也最大,錶明PELFM的耐熱性更好,熱穩定性更彊。
이개성감목질소여취을희순( PVA)위원료,갑철위교련제,채용무궤발포원리,제비료취을희순/감목질소발포재료( PLFM)、취을희순/배양화감목질소발포재료( PELFM)화취을희순/간갑기화감목질소발포재료( PHLFM),병이용홍외광보、소묘전경、DSC급TG대발포재료진행료측정급분석。결과표명, PVA용량위5 g시,배양화감목질소용량위50%(이 PVA 질량계,하동),갑철용량24%,류산용량54%,고화온도120℃제비적 PELFM 랍신강도최대,위17.26 MPa。 FT-IR분석현시, PLFM화PHLFM적분배5위균발생취대,이PELFM몰유발생취대;SEM도편현시발포재료적공경불규칙,공극솔교대;여령량충발포재료상비,PELFM랍신성능저,표관밀도교저,흡수배솔야교저。종DSC화TG분석가지,3충발포재료중PELFM구유교저적파리태전변온도,단기생물상용성최호,PELFM실중솔최고봉대응적봉치온도최대차개우감목질소여PVA지간,소실후잔여량야최대,표명PELFM적내열성경호,열은정성경강。
By using inorganic foaming principles,polyvinyl alcohol/alkali lignin foaming material(PLFM),polyvinyl alcohol/epoxided alkali lignin foaming material ( PELFM ) , and polyvinyl alcohol/hydroxymethylated alkali lignin foaming material ( PHLFM ) , were prepared,with polyvinyl alcohol and modified alkali lignin as raw materials and formaldehyde as crosslinking agent. Then they were determined and analyzed by FT-IR,scanning electron microscope,DSC,and TG. The results showed that when PVA was 5g and the addition of epoxided alkali lignin was 50% of the PVA’ s mass,formaldehyde 24%,sulfuric acid 54%,and 120℃ for solidification, the obtained PELFM had the maximum tensile strength,17. 26 MPa. FT-IR results showed that substitutions were occurred on the benzene rings of PLFM and PHLFM at the 5-position,but PELFM not. SEM maps showed that the pore sizes were irregular and the porosity was large. Compared with others, PELFM possessed lower tensile property, apparent density, and water absorbency. From DSC and TG analysis,PELFM had the lowest glass transition temperature,the best biological compatibility,the maximum residual quantity and the maximum temperature corresponding to the highest lose rate peak. This temperature which was between the relevant temperatures of alkali lignin and PVA. It indicated that PELFM had the best heat resistance and thermal stability.