高校化学工程学报
高校化學工程學報
고교화학공정학보
JOURNAL OF CHEMICAL ENGINEERING OF CHINESE UNIVERSITIES
2014年
4期
719-724
,共6页
两面针%氯化两面针碱%内部沸腾法%提取%纯化
兩麵針%氯化兩麵針堿%內部沸騰法%提取%純化
량면침%록화량면침감%내부비등법%제취%순화
zanthoxylum nitidum%nitidine chloride%inner ebullition%extraction%purification
为降低两面针生物碱提取过程酸对设备的腐蚀及提高纯化过程的回收率,采用了加酸内部沸腾法强化提取氯化两面针碱,提取液直接用阳离子交换树脂吸附及超声波辅助强化洗脱在树脂表面结晶出来的两面针生物碱晶体。实验结果表明:两面针粉末先用4倍物料量的乙醇盐酸解吸剂解吸,解吸剂中盐酸和乙醇的质量浓度分别为0.61%和80%,然后用16倍物料量的20%质量浓度的乙醇在82℃下提取4 min,在此条件下氯化两面针碱提取得率为0.134%;用732阳离子交换树脂直接在40℃下静态吸附133倍树脂用量的内部沸腾法提取液,用盐酸浓度为3 mol·L-1、乙醇质量浓度为70%的酸乙醇洗脱液在超声波的辅助下间歇解吸附,解吸率达到99%以上,分离得到的氯化两面针碱纯度为94.5%,回收率为77.7%。与传统酸醇回流提取对比,加酸内部沸腾法提取快37.5倍、乙醇和盐酸消耗量减少一倍,对设备腐蚀大为减轻,提取液可以用阳离子交换树脂直接富集分离,氯化两面针碱回收率提高24.2%。
為降低兩麵針生物堿提取過程痠對設備的腐蝕及提高純化過程的迴收率,採用瞭加痠內部沸騰法彊化提取氯化兩麵針堿,提取液直接用暘離子交換樹脂吸附及超聲波輔助彊化洗脫在樹脂錶麵結晶齣來的兩麵針生物堿晶體。實驗結果錶明:兩麵針粉末先用4倍物料量的乙醇鹽痠解吸劑解吸,解吸劑中鹽痠和乙醇的質量濃度分彆為0.61%和80%,然後用16倍物料量的20%質量濃度的乙醇在82℃下提取4 min,在此條件下氯化兩麵針堿提取得率為0.134%;用732暘離子交換樹脂直接在40℃下靜態吸附133倍樹脂用量的內部沸騰法提取液,用鹽痠濃度為3 mol·L-1、乙醇質量濃度為70%的痠乙醇洗脫液在超聲波的輔助下間歇解吸附,解吸率達到99%以上,分離得到的氯化兩麵針堿純度為94.5%,迴收率為77.7%。與傳統痠醇迴流提取對比,加痠內部沸騰法提取快37.5倍、乙醇和鹽痠消耗量減少一倍,對設備腐蝕大為減輕,提取液可以用暘離子交換樹脂直接富集分離,氯化兩麵針堿迴收率提高24.2%。
위강저량면침생물감제취과정산대설비적부식급제고순화과정적회수솔,채용료가산내부비등법강화제취록화량면침감,제취액직접용양리자교환수지흡부급초성파보조강화세탈재수지표면결정출래적량면침생물감정체。실험결과표명:량면침분말선용4배물료량적을순염산해흡제해흡,해흡제중염산화을순적질량농도분별위0.61%화80%,연후용16배물료량적20%질량농도적을순재82℃하제취4 min,재차조건하록화량면침감제취득솔위0.134%;용732양리자교환수지직접재40℃하정태흡부133배수지용량적내부비등법제취액,용염산농도위3 mol·L-1、을순질량농도위70%적산을순세탈액재초성파적보조하간헐해흡부,해흡솔체도99%이상,분리득도적록화량면침감순도위94.5%,회수솔위77.7%。여전통산순회류제취대비,가산내부비등법제취쾌37.5배、을순화염산소모량감소일배,대설비부식대위감경,제취액가이용양리자교환수지직접부집분리,록화량면침감회수솔제고24.2%。
In order to reduce equipment corrosion during typical zanthoxylum nitidum alkaloid extraction processes and improve nitidine chloride yield during purification processes, an acid inner ebullition method was used to intensify the extraction of nitidine chloride. The zanthoxylum nitidum alkaloid in the extraction solution is directly adsorbed by cationic exchange resins, and then desorbed under ultrasonication. The experimental results show that when the zanthoxylum nitidum powder is immersed into 4 mL·g-1 solvent (which was composed of 80%(wt) ethanol and 0.61%(wt) HCl), and then extracted by 16 mL·g-1 of another solvent (which was composed of 20%(wt) ethanol) at 82℃ for 4 min, the yield of nitidine chloride is 0.134%. The extraction solution is treated with cationic exchange resin 732 at 40℃ (the ratio between the extraction solution and the resin is 133:1) and the adsorbed zanthoxylum nitidum alkaloid was desorbed in acid ethanol under ultrasonication. The desorption ratio, nitidine chloride yield and the purity of nitidine chloride are 99%, 77.7%and 94.5%, respectively. Compared with the acid ethanol refluxing extraction, the acid inner ebullition possesses much higher reaction rate (up to 37.5 times) and also consumes less ethanol and chloride acid (up to 50%), which reduces equipment corrosion. In addition, the extraction solution was directly purified by the cationic exchange resin and the nitidine chloride yield is improved by 24.2%.