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研究生:戴志全
研究生(外文):Chih-Chyuan Tai
論文名稱:澱粉-蔗糖酯複合物之形成對高直鏈玉米澱粉與關華豆膠相容性、黏度及失水率之影響
論文名稱(外文):Effect of the HylonⅦ-Sucrose Ester Complex Formation on Compatibility, Viscosity and Water Loss of the HylonⅦ-Guar Gum Mixture
指導教授:陳堂
指導教授(外文):John T. Chien
學位類別:碩士
校院名稱:輔仁大學
系所名稱:食品營養學系
學門:醫藥衛生學門
學類:營養學類
論文種類:學術論文
論文出版年:2000
畢業學年度:88
語文別:中文
論文頁數:130
中文關鍵詞:高直鏈玉米澱粉蔗糖酯關華豆膠相容性玻璃轉化溫度sub-Tg黏度
外文關鍵詞:HylonVIIsucrose esterguar gumCompatibilityTgsub-Tgviscosity
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  • 被引用被引用:6
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不相容的澱粉與多醣類分子會相互排擠,造成自分子聚集而加速澱粉老化。因此提高澱粉與多醣類之相容性,則可改善含澱粉食品品質及物性性質。本研究擬將高親水性之蔗糖酯(P-1670)與高直鏈玉米澱粉(HylonⅦ)複合,探討複合後所造成裸露之蔗糖基是否增加在水溶液中與關華豆膠分子外端分支接觸的機會,以及提高HylonⅦ與關華豆膠之相容性。實驗以玻璃轉化溫度(Tg)變化來評估兩成份之相容程度,亦透過失水率和黏度分析來了解相容性對膠體結構之影響。
示差掃描熱分析(DSC)的結果顯示,HylonⅦ於79.9℃、複合物在97.3℃及關華豆膠於56.6, 68.4和97.8℃呈現Tg。HylonⅦ-關華豆膠混合膠體雖在66.7℃仍存在關華豆膠的Tg,但原HylonⅦ的Tg已消失。反觀複合物-關華豆膠混合膠體,不但原成份的Tg消失,且在80.4℃另出現異於原成份的新Tg。以動態機械分析(DMA)亦發現,HylonⅦ或複合物與關華豆膠之混合膠體分別在92.2℃和104.5℃均出現新Tg。原成份的Tg雖然存在,但其tagδ的波峰高度均已下降,顯示因混合後各成份分子間,因部份相容所造成交互作用,而降低分子移動之體積分率。故由Tg分析結果可知HylonⅦ或複合物與關華豆膠均呈現部份相容,且複合物與關華豆膠之相容程度高於HylonⅦ-關華豆膠混合膠體者。各樣品在Tg以下溫度均發現sub-Tg及sub-Tg焓,其成因可能與聚合物側鏈分子之移動性有關。
膠體於90±2℃之失水率分析發現,關華豆膠之添加可降低HylonⅦ及複合物的失水率,顯示兩相容之成份可明顯改善混合膠體之保水性。但複合物-關華豆膠混合膠體之失水率高於HylonⅦ-關華豆膠混合膠體者,這可能與HylonⅦ和蔗糖酯複合後的水合體積改變有關。
HylonⅦ、複合物、關華豆膠及其混合膠體貯存前、後,於25.5±0.1℃的之視黏度依序均為:HylonⅦ-關華豆膠混合膠體>複合物-關華豆膠混合膠體>關華豆膠>複合物> HylonⅦ。且HylonⅦ或複合物與關華豆膠混合膠體之視黏度均高於其個別成份視黏度之加成。由此可知,兩部份相容成份之混合可提高混合膠體之視黏度。此與失水率分析之趨勢相同。各膠體經貯存1天後的視黏度均高於未經貯存者,顯示膠體強度會因貯存而增強。
各膠體溶液的n值均介於0與1之間(0<n<1),故均屬於偽膠流體。添加蔗糖酯或關華豆膠均會降低HylonⅦ的n值,提高其偽膠特性。貯存一天後,HylonⅦ的n值由0.73降為0.47,可能因貯存導致自分子聚集,或因直鏈澱粉與支鏈澱粉之不相容所致。複合物、關華豆膠、HylonⅦ-關華豆膠混合膠體及複合物-關華豆膠混合膠體之n值則不因貯存而改變,此可能因HylonⅦ或複合物分別與關華豆膠部份相容,而提高兩成份異分子間之交互作用,或因直鏈澱粉與蔗糖酯之複合作用抑制澱粉自分子聚集之故。
Incompatibility between starch and polysaccharide may result to form self-aggregation of individual molecules in an aqueous solution, and lead to retrogradation of starch. The quality and physical properties of starch-containing foods were thus degraded. This could be improved by increasing compatibility between starch and polysaccharide. Complex formation of sucrose ester and starch was also commonly used to retard starch retrogradation. It was of interest to investigate whether the complex may also increase compatibility between guar gum and HylonⅦ, amylomaize starch with 58.8% amylose content. In this study, compatibility of two components was investigated by changes in glass transition temperatures (Tg). Water loss and viscosity analysis can subsequently be used to monitor the influence of compatibility on the gel.
Results of differential scanning calorimetry (DSC) showed that HylonⅦ and the complex appeared glass transitions at 79.9℃ and 97.3℃, respectively, whereas, Tgs for guar gum were at 56.6, 68.4, 97.8℃. The HylonⅦ-guar gum mixture, appeared Tg at 66.7℃, which was close to the Tg of guar gum, however, the Tg of HylonⅦ was disappeared. On the other hand, the complex-guar gum no longer showed the Tgs of two individual components, and exhibited a new Tg at 80.4℃, which was significantly different from the Tgs of two individual components. Similarly, results of dynamic mechanical analysis (DMA) appeared a new Tg at 92.2℃and 104.5℃ for the HylonⅦ-guar gum and complex-guar gum mixture, respectively. Although the Tgs of individual the components were still appeared in the above mixtures, the heights of tanδ peaks declined. Above evidence implies that interaction, which led to close contact between two partially compatible molecules in a mixed gel, decreased the volume fraction of the relaxing phase. Both HylonⅦ and the complex were partial compatible with guar gum, and the complex-guar gum mixture shows higher compatibility than the corresponding HylonⅦ-guar gum mixture. All the samples appeared the sub-Tgs and sub-Tg endotherms below the corresponding Tgs. The sub-Tg relaxation may relate to side-chain relaxation of a polymer.
Addition of guar gum decreased water loss of HylonⅦ and the complex, while being heated at 90±2℃. This result indicates that water holding capacity of a mixed gel was significant improved by mixing two compatible components. Water loss of the complex-guar gum mixture was higher than that of the HylonⅦ-guar gum mixture. This was due to change in hydrodynamic volume for the complex.
Apparent viscosity of above samples at 25.5±0.1℃ were as follows: the HylonⅦ-guar gum mixture > the complex-guar gum mixture > guar gum > the complex > HylonⅦ. Apparent viscosities of the HylonⅦ-guar gum and complex-guar gum mixtures were higher than the sum of viscosities of individual components. This result shows that apparent viscosity increased with mixing two compatible components. Apparent viscosity of the HylonⅦ-guar gum mixture was higher than that of the complex-guar gum mixture. Viscosity results were consistent with those of water loss. After one day of storage, all the gels showed higher apparent viscosities than those of no storage. It means that the gel strength increased during storage.
All the mixtures showed pseudoplastic behavior (0<n<1). The n value of HylonⅦ decreased after complexing with sucrose ester or mixing with guar gum. After one day of storage, the n value of HylonⅦ decreased from 0.73 to 0.47, which may result from self-aggregation of starch molecules, or incompatibility of amylose and amylopectin. On the other hand, the n values of the complex, guar gum, and the mixture remained the same during storage. This was due to partial compatibility between HylonⅦ (or complex) and guar gum, which leaded to an increase of inter-molecular interaction. Starch retrogradation was thus inhibited.
第一章 緒 言 1
第二章 文獻回顧 3
一、澱粉的結構與糊化特性 3
二、澱粉和乳化劑的交互作用 12
(一)澱粉和乳化劑的交互作用形式 12
(二)澱粉-乳化劑複合物形成的影響因素 17
(三)乳化劑與脂質對澱粉流變性質的影響 31
三、澱粉與食用膠的交互作用 35
(一)澱粉與食用膠的相容性 35
(二)流變性質與失水率變化 39
四、玻璃轉化現象 48
(一)玻璃轉化溫度與相容性 48
(二)玻璃轉化溫度的影響因子 57
1 聚合物組成與分子量 57
2 交互作用 58
3 聚合物結晶程度 60
4 塑化劑的影響 63
(三)澱粉Tg以下的熱轉換 64
第三章 材料與方法 79
一、材料 79
二、方法 80
(一)水分含量測定 80
(二)直鏈澱粉定量 80
(三)澱粉糊化 81
(四)HylonⅦ複合物製備 81
(五)混合膠體製備 82
(六)示差掃描熱分析 82
1 糊化溫度測定 82
2 複合量之測定 83
3 Tg及sub-Tg焓測定 83
(七)動態機械分析 84
(八)失水率分析 84
(九)黏度分析 84
(十)統計分析 85
第四章 結果與討論 86
一、高直鏈玉米澱粉的糊化 86
二、飽和複合量測定 88
三、玻璃轉化溫度與相容性 91
(一)示差掃描熱分析 91
(二)動態機械分析 99
四、失水率分析 106
五、黏度分析 109
第五章 結 論 117
參考文獻 119
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