天津工业大学学报
天津工業大學學報
천진공업대학학보
JOURNAL OF TIANJIN POLYTECHNIC UNIVERSITY
2014年
5期
39-43
,共5页
杨俊玲%赵福龙%夏军%张晓波%王璇
楊俊玲%趙福龍%夏軍%張曉波%王璇
양준령%조복룡%하군%장효파%왕선
高脱乙酰度壳聚糖%水溶性壳寡糖%水溶性壳寡糖 Fe(Ⅲ)配合物
高脫乙酰度殼聚糖%水溶性殼寡糖%水溶性殼寡糖 Fe(Ⅲ)配閤物
고탈을선도각취당%수용성각과당%수용성각과당 Fe(Ⅲ)배합물
HD-chitosan%soluble COS%soluble COS-Fe(Ⅲ)complex
以皮皮虾壳作基本原料,分别采用稀盐酸、稀碱溶液浸泡,除去虾壳中的钙质等无机质和蛋白等有机成分,以浓碱脱除甲壳素上的乙酰基,制得壳聚糖.再以其为原料,采用 H2O2氧化降解法得到水溶性壳寡糖.将所制水溶性壳寡糖加入到氯化铁溶液中,设定各项条件,使二者进行配位反应.经系列实验证实,得出制备高脱乙酰度壳聚糖最适宜条件为:温度85℃,时间9 h,NaOH 质量分数45%,料液比1:300.所得产品脱乙酰度为89.6%,收率(壳聚糖/甲壳素)为73.1%,其他各项指标也均为优良级.制备水溶性壳寡糖最适宜条件为:温度65℃,时间6 h,醋酸质量分数4.0%,H2O2质量分数4.0%,产品平均粘均分子质量为2.9 ku,外观为淡黄色粉末,溶解性能优良.通过对 FT-IR 和 UV 谱图的分析,证实了水溶性壳寡糖 Fe(Ⅲ)配合物的生成.
以皮皮蝦殼作基本原料,分彆採用稀鹽痠、稀堿溶液浸泡,除去蝦殼中的鈣質等無機質和蛋白等有機成分,以濃堿脫除甲殼素上的乙酰基,製得殼聚糖.再以其為原料,採用 H2O2氧化降解法得到水溶性殼寡糖.將所製水溶性殼寡糖加入到氯化鐵溶液中,設定各項條件,使二者進行配位反應.經繫列實驗證實,得齣製備高脫乙酰度殼聚糖最適宜條件為:溫度85℃,時間9 h,NaOH 質量分數45%,料液比1:300.所得產品脫乙酰度為89.6%,收率(殼聚糖/甲殼素)為73.1%,其他各項指標也均為優良級.製備水溶性殼寡糖最適宜條件為:溫度65℃,時間6 h,醋痠質量分數4.0%,H2O2質量分數4.0%,產品平均粘均分子質量為2.9 ku,外觀為淡黃色粉末,溶解性能優良.通過對 FT-IR 和 UV 譜圖的分析,證實瞭水溶性殼寡糖 Fe(Ⅲ)配閤物的生成.
이피피하각작기본원료,분별채용희염산、희감용액침포,제거하각중적개질등무궤질화단백등유궤성분,이농감탈제갑각소상적을선기,제득각취당.재이기위원료,채용 H2O2양화강해법득도수용성각과당.장소제수용성각과당가입도록화철용액중,설정각항조건,사이자진행배위반응.경계렬실험증실,득출제비고탈을선도각취당최괄의조건위:온도85℃,시간9 h,NaOH 질량분수45%,료액비1:300.소득산품탈을선도위89.6%,수솔(각취당/갑각소)위73.1%,기타각항지표야균위우량급.제비수용성각과당최괄의조건위:온도65℃,시간6 h,작산질량분수4.0%,H2O2질량분수4.0%,산품평균점균분자질량위2.9 ku,외관위담황색분말,용해성능우량.통과대 FT-IR 화 UV 보도적분석,증실료수용성각과당 Fe(Ⅲ)배합물적생성.
HD -chitosan was produced with basic material -mantis shrimp shell which was removed inorganic salt with chlorhydric acid, proteins with dilute alkali solution, then dislodged acetyl group with concentrated alkaline solution. Next, the above -mentioned HD -chitosan was degraded with H2O2 for producing soluble COS. With adjusted conditions, the soluble COS was added to ferric chloride solution for complexing. It was confirmed by series of experiments that the optimized conditions of preparing HD-chitosan was 45%NaOH, the ratio of material to solvent(g/ml)1 : 300, and at constant temperature 85 ℃ for 9 h. The yield of HD-chitosan to chitin was 73.1%with other excellent quality index. The optimized conditions of preparing soluble oligosaccharide was 4.0% acetic acid, 4.0% H2O2 and at constant temperature 65 ℃ for 6 h. The viscosity average molecular weigh of products was 2.9 ku. In addition, it was also observed that the products of oligosaccharide was desirable faint yellow powder and had fine solubility. According to analysis of FT-IR and UV spectrum, the formation of soluble COS-Fe (Ⅲ) complex was certified.