嘉应学院学报
嘉應學院學報
가응학원학보
JOURNAL OF JIAYING UNIVERSITY
2012年
5期
53-56
,共4页
Fe3O4磁性微球%琼脂%聚乙二醇
Fe3O4磁性微毬%瓊脂%聚乙二醇
Fe3O4자성미구%경지%취을이순
Fe3O4 magnetic microsphere%agar%polyethylene glycol
用共沉淀法制备Fe304磁性粒子,选用聚乙二醇和琼脂制备核/双壳医用磁性微球.最佳工艺条件为:Fe2+/Fe2+之比在1.70~1.75;沉淀剂25%NH3·H2O过量20~30%,在温度35℃,pH值11,反应时间为1h;琼脂的包覆最佳温度为50℃,pH值为9,时间lh;聚乙二醇包裹最佳温度为55℃,pH值为4,时间1h,可以通过调节搅拌速度和超声波分散时间控制Fe3O4粒子的尺度,实验确定包覆剂用量.并用透射电镜、分光光度计、古埃磁天平等进行了初步表征.
用共沉澱法製備Fe304磁性粒子,選用聚乙二醇和瓊脂製備覈/雙殼醫用磁性微毬.最佳工藝條件為:Fe2+/Fe2+之比在1.70~1.75;沉澱劑25%NH3·H2O過量20~30%,在溫度35℃,pH值11,反應時間為1h;瓊脂的包覆最佳溫度為50℃,pH值為9,時間lh;聚乙二醇包裹最佳溫度為55℃,pH值為4,時間1h,可以通過調節攪拌速度和超聲波分散時間控製Fe3O4粒子的呎度,實驗確定包覆劑用量.併用透射電鏡、分光光度計、古埃磁天平等進行瞭初步錶徵.
용공침정법제비Fe304자성입자,선용취을이순화경지제비핵/쌍각의용자성미구.최가공예조건위:Fe2+/Fe2+지비재1.70~1.75;침정제25%NH3·H2O과량20~30%,재온도35℃,pH치11,반응시간위1h;경지적포복최가온도위50℃,pH치위9,시간lh;취을이순포과최가온도위55℃,pH치위4,시간1h,가이통과조절교반속도화초성파분산시간공제Fe3O4입자적척도,실험학정포복제용량.병용투사전경、분광광도계、고애자천평등진행료초보표정.
Fe3O4 magnetic microsphere was prepared by coprecipitation method and medical nucleonic/bivalve mag- netic microsphere was prepared by polyethylene glycol or agar. The optimal condition of prepared Fe3O4 magnetic microsphere was that the ratio of Fe3+/Fe2+ was between 1.70 20 -30%, and the reaction time was lh at 35℃, and pH ic/bivalve magnetic microsphere was that the coating time time with polyethylene glycol was lh at 55℃, pH with 4. and 1.75; 25% NH3 H2O precipitant was above value was 11. The optimal condition of medical nucleon- with agar was lh at 50℃, pH with 9, and the coating The size of Fe3O4 was controlled by stirring speed and ul- trasonic. The characterizations of materials were investigated by projection electron microscopy, spectrophotometer and magnetic balance.