將藥材投入提取罐內，加藥材的5～10倍的溶媒如水、乙醇、甲醇、丙酮等(據工藝要求)。開啟提取罐直通和夾套蒸汽閥門，使提取液加熱至沸騰20～30分鐘后，用抽濾管將1/3提取液抽入濃縮器。關閉提取罐直通和夾套蒸汽、開啟加熱器閥門使液料進行濃縮。濃縮時產生二次蒸汽，通過蒸發器上升管送入提取罐作提取的熱源和溶液，維持提取罐內沸騰。

分(fen)批(pi)空(kong)氣(qi)壓(ya)縮立即回升，經氣(qi)液(ye)(ye)分(fen)離器(qi)器(qi)氣(qi)液(ye)(ye)分(fen)離器(qi)成熱氣(qi)液(ye)(ye)分(fen)離器(qi)液(ye)(ye)，暴跌到(dao)截(jie)(jie)取(qu)(qu)(qu)堿(jian)罐(guan)作新容(rong)劑加到(dao)藥(yao)表面上(shang)，新容(rong)劑由上(shang)而下快速(su)路(lu)使(shi)用(yong)(yong)中(zhong)(zhong)(zhong)草中(zhong)(zhong)(zhong)草藥(yao)村(cun)層到(dao)截(jie)(jie)取(qu)(qu)(qu)罐(guan)側面,中(zhong)(zhong)(zhong)草中(zhong)(zhong)(zhong)草藥(yao)村(cun)中(zhong)(zhong)(zhong)的(de)可溶(rong)(rong)(rong)解性性很好含量溶(rong)(rong)(rong)解性于截(jie)(jie)取(qu)(qu)(qu)堿(jian)罐(guan)容(rong)劑。截(jie)(jie)取(qu)(qu)(qu)液(ye)(ye)經抽濾管抽入浸(jin)提(ti)咖(ka)(ka)啡器(qi)、浸(jin)提(ti)咖(ka)(ka)啡出現的(de)分(fen)批(pi)空(kong)氣(qi)壓(ya)縮又送去截(jie)(jie)取(qu)(qu)(qu)罐(guan)作供熱系(xi)統和新容(rong)劑，這(zhe)樣一(yi)來產生的(de)新容(rong)劑大(da)分(fen)流截(jie)(jie)取(qu)(qu)(qu)，故(gu)中(zhong)(zhong)(zhong)草中(zhong)(zhong)(zhong)草藥(yao)村(cun)中(zhong)(zhong)(zhong)溶(rong)(rong)(rong)質(zhi)(zhi)強(qiang)度與容(rong)劑中(zhong)(zhong)(zhong)含溶(rong)(rong)(rong)質(zhi)(zhi)強(qiang)度持續高(gao)等度，中(zhong)(zhong)(zhong)草中(zhong)(zhong)(zhong)草藥(yao)村(cun)中(zhong)(zhong)(zhong)的(de)溶(rong)(rong)(rong)質(zhi)(zhi)快速(su)路(lu)總混(hun)，直(zhi)齊全總混(hun)(截(jie)(jie)取(qu)(qu)(qu)液(ye)(ye)無(wu)色透(tou)明(ming)的(de)透(tou)明(ming)的(de))，這(zhe)段時間(jian)，截(jie)(jie)取(qu)(qu)(qu)液(ye)(ye)中(zhong)(zhong)(zhong)止抽入浸(jin)提(ti)咖(ka)(ka)啡器(qi)，浸(jin)提(ti)咖(ka)(ka)啡的(de)分(fen)批(pi)空(kong)氣(qi)壓(ya)縮轉(zhuan)送待風冷卻器(qi)，浸(jin)提(ti)咖(ka)(ka)啡立即參(can)與，直(zhi)浸(jin)提(ti)咖(ka)(ka)啡成必須比例(1.2～1.34)的(de)乳膏，發出被用(yong)(yong)。截(jie)(jie)取(qu)(qu)(qu)堿(jian)罐(guan)的(de)無(wu)色透(tou)明(ming)的(de)透(tou)明(ming)的(de)液(ye)(ye)態物(wu)質(zhi)(zhi)，可置入貯罐(guan)作下批(pi)復文件用(yong)(yong)，藥(yao)渣(zha)從出渣(zha)門排掉，若果用(yong)(yong)有(you)機化學(xue)容(rong)劑截(jie)(jie)取(qu)(qu)(qu)，則先加恰當的(de)水，開連(lian)通和夾套(tao)空(kong)氣(qi)壓(ya)縮，回報容(rong)劑后，將渣(zha)排掉。

藥草多工作生成(cheng)萃取專用設(she)備(bei) 作物生成(cheng)罐其主(zhu)要方法性(xing)能(neng)