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研究生: 郭柏慶
Bo-ching Guo
論文名稱: 果膠之萃取與鑑定
Extraction and characterization of pectins
指導教授: 陳崇賢
Chorng-Shyan Chern
口試委員: 黃延吉
Yan-Jyi Huang
許榮木
Rung-Mu Shiu
學位類別: 碩士
Master
系所名稱: 工程學院 - 化學工程系
Department of Chemical Engineering
論文出版年: 2014
畢業學年度: 102
語文別: 中文
論文頁數: 86
中文關鍵詞: 果膠萃取流變性質
外文關鍵詞: pectin, extraction, rheological properties
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本研究首先對市售的6樣中國果膠及6樣德國果膠進行流變實驗,研究其視黏度、極限黏度、分子量以及在不同pH值、溫度、剪切率下所得的視黏度。結果顯示,果膠屬於剪切稀釋的流體。果膠相對分子量分佈範圍為40~65萬Da之間,極限黏度為1.5~4.5(dL/g),分子量和極限黏度有一線性關係,分子量越高的果膠其極限黏度也就越大。視黏度和極限黏度也有著視黏度越大極限黏度越大的關係。高甲氧基果膠對於溫度的敏感程度相對於非高甲氧基還低。接著使用工業上常用的酸提取法對柳丁皮進行果膠的提取,藉由改變pH值、萃取溫度及萃取時間來決定得到最佳產率的條件。結果顯示,在pH 2.5、提取溫度90 ℃、萃取時間2小時可以得最佳產率。並對自行萃取的果膠進行FTIR以及GPC的測量,結果顯示,大部份測定出的中國果膠和自製果膠為高甲氧基果膠,而德國果膠則多屬於高低甲氧基差不多的果膠。


In this study, six commercial Chinese pectin samples and six commercial German pectin samples were investigated primary by using rheological experiments such as apparent viscosity, intrinsic viscosity, molecular weight in different pH values, temperature and shear rate. The results showed that aqueous pectin solution are shear-thinning fluids. Pectin’s molecular weight is between 40,0000 and 650,000 Da, and pectin’s intrinsic viscosity is from 1.5 to 4.5 dL/g. Molecular weight and intrinsic viscosity exhibit a linear correlation. The higher the molecular weight of pectin, the greater the intrinsic viscosity of pectin. Apparent viscosity and intrinsic viscosity also have positive linear correlation. High-methoxy pectin is less sensitive to change in temperature than other kinds of pectin. Common acid extraction method to extract pectin by changing the PH value, temperature and extraction time was used to determine the optimum conditions for yield. The results showed that in pH 2.5, extraction temperature 90 ℃, extraction time 2 hours can give the optimum yield. We also performed the FTIR and GPC measurements test, the results showed that our pectin and commercial Chinese pectins are almost high-methoxy pectin and commercial German pectins are almost medium-methoxy pectin.

目錄 摘要 I Abstract II 致謝 III 目錄 V 表目錄 VII 圖目錄 VIII 第一章序論 1 1-1研究背景與目的 1 1-2研究內容及簡介 2 第二章 文獻回顧 3 2-1果膠概述 3 2-2果膠萃取 4 2-2-1酸萃取法 5 2-2-2鹼化脫酯萃取法 5 2-2-3微波萃取法 5 2-2-4螯合劑添加法 6 2-2-5超高壓萃取法 6 2-2-6次臨界流體萃取法 6 2-2-7果膠的沉澱 7 2-3果膠的凝膠機制 7 2-4流變學 8 2-5黏度 9 2-6流變儀 10 2-6-1 U形管黏度計 11 2-6-2旋轉式黏度計 11 2-7流體流變圖 12 2-8震盪試驗 14 2-8-1動態試驗 14 2-8-2靜態試驗 15 2-9傅立葉紅外線光譜儀 15 2-10膠體滲透層析儀 17 第三章 實驗藥品、設備及方法 20 3-1藥品 20 3-2實驗儀器及設備 21 3-3實驗方法 22 3-3-1果膠的視黏度測定 22 3-3-2果膠的極限黏度測定 23 3-3-3果膠在加入蔗糖後視黏度的變化 24 3-3-4果膠在加入蔗糖後改變pH值其視黏度的變化 25 3-3-5改變溫度對視黏度的影響 26 3-3-6黏度與剪切率的測量 26 3-3-7傅立葉紅外線光譜儀測定 27 3-3-8膠體滲透層析儀測定 28 3-3-9果膠萃取 28 3-3-10自製果膠的測量 29 第四章 結果與討論 30 4-1果膠的視黏度測定 30 4-2果膠的極限黏度測定 33 4-3果膠在加入蔗糖後視黏度的變化 44 4-4果膠在加入蔗糖後改變pH值其視黏度的變化 46 4-5改變溫度對視黏度的影響 50 4-6黏度與剪切率的測量 54 4-7傅立葉紅外線光譜儀測定 63 4-8膠體滲透層析儀測定 70 4-9果膠萃取 71 4-10自製果膠的測量 72 4-11綜合討論-極限黏度與分子量的關係 80 4-12綜合討論-極限黏度與視黏度的關係 81 第五章 結論 83 參考文獻 84

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