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Effects of chemical structure of common monosaccharides and polyols on plasticization and antiplasticization of starch films.

机译:普通单糖和多元醇的化学结构对淀粉膜增塑和抗塑化的影响。

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摘要

Monosaccharides have several hydroxyl groups and a compatible structure with starch polymers likely resulting in effective plasticization in starch films. Two groups of plasticizers (polyols and monosaccharides) were used to compare their plasticizing efficiency. Fructose, glucose, mannose, galactose, glycerol, sorbitol, ethylene glycol and maltitol were selected at 13.031 mmol per 100 g of pea starch. Edible starch films were produced after heat gelatinization and dehydration of the 3% starch dispersion. The microstructure, attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) characteristics, thickness, moisture content, tensile strength, modulus of elasticity, elongation-at-break, water vapor permeability, and transparency of films were determined. Microstructure of the film solutions showed that some swollen starch granules and their remnants existed in the film. Compared to the FTIR spectra of pure starch films, the spectra of plasticized films showed that more hydrogen bound hydroxyl groups and more water molecules were attracted around starch polymer chains. Monosaccharide-plasticized films were comparable to the polyol-plasticized films in parameters determined from the tensile test, but were more resistant in moisture permeation than the polyol-plasticized films. It was assumed that the structural compatibility of monosaccharides with starch might result in a denser polymer-plasticizer complex, smaller size of free volume, and less segmental motions of starch chains. In conclusion, monosaccharides were identified as effective plasticizers for starch film.;According to the study results, the recommended plasticizer concentration for plasticization of the starch films is as follows: Fructose is in the range of 4.34 to 10.87 mmol at almost entire RH. Mannose and glucose should be from 4.34 to 8.69 mmol at RH below 50%. Otherwise, the crystallization occurs. Glycerol can have a broader range. Sorbitol is like glucose. Its concentration will be below 8.69 mmol in case of crystallization occurs. (Abstract shortened by UMI.).;Effect of plasticizer content (4.34 to 10.87 mmol per g of dry starch) and storage relative humidity (RH) (11.3% to 75.4%) on moisture content (MC), tensile strength (TS), elongation (E), modulus of elasticity (EM), and water vapor permeability (WVP) were evaluated using response surface methodology. EG was dropped, because during the experiments the EG film became brittle at low EG concentration level and low RH conditions. MC was influenced strongly by RH. Glycerol-plasticized films had the highest MC, indicating that water molecules played a more important role in plasticizing starch films. Monosaccharidc-plasticized films and polyol-plasticized films had similar TS values. However, monosaccharide-plasticized films had higher E values and lower EM values than polyol-plasticized films, meaning monosaccharides had better efficiency in plasticizing starch films. Recrystallization happened in glucose- and sorbitol-plasticized films when they were stored in high RH. Sorption isotherm studies showed similar adsorption and desorption profiles for all three monosaccharide-plasticized films and hysteresis. Flory-Huggins model fitted experimental data best for starch films, while BET model fitted the data marginally.
机译:单糖具有几个羟基并且与淀粉聚合物具有相容的结构,这可能导致淀粉薄膜有效地增塑。使用两组增塑剂(多元醇和单糖)比较它们的增塑效率。每100克豌豆淀粉选择的果糖,葡萄糖,甘露糖,半乳糖,甘油,山梨糖醇,乙二醇和麦芽糖醇的含量为13.031 mmol。在3%淀粉分散体热糊化和脱水之后,产生可食用的淀粉膜。测定了薄膜的微观结构,衰减全反射傅里叶变换红外光谱(ATR-FTIR)特性,厚度,水分,拉伸强度,弹性模量,断裂伸长率,水蒸气透过率和薄膜透明度。薄膜溶液的微观结构表明,薄膜中存在一些溶胀的淀粉颗粒及其残余物。与纯淀粉薄膜的FTIR光谱相比,增塑薄膜的光谱表明,更多的氢键合羟基和更多的水分子被淀粉聚合物链吸引。从拉伸试验确定的参数上,单糖增塑膜可与多元醇增塑膜相比,但与多元醇增塑膜相比,其抗透湿性更高。据推测,单糖与淀粉的结构相容性可能导致致密的聚合物-增塑剂复合物,较小的自由体积尺寸和较少的淀粉链段运动。总之,单糖被认为是淀粉膜的有效增塑剂。根据研究结果,建议用于淀粉膜增塑的增塑剂浓度如下:在几乎整个RH下,果糖的浓度范围为4.34至10.87 mmol。相对湿度低于50%时,甘露糖和葡萄糖应为4.34至8.69 mmol。否则,发生结晶。甘油的范围更广。山梨糖醇就像葡萄糖。如果发生结晶,其浓度将低于8.69 mmol。 (摘要由UMI缩短。);增塑剂含量(每克干淀粉4.34至10.87 mmol)和储存相对湿度(RH)(11.3%至75.4%)对水分含量(MC),抗张强度(TS)的影响,伸长率(E),弹性模量(EM)和水蒸气渗透性(WVP)使用响应表面方法进行了评估。下降了EG,因为在实验过程中,EG膜在低EG浓度水平和低RH条件下变脆。 MC受到RH的强烈影响。甘油增塑膜的MC最高,表明水分子在淀粉膜增塑中起着更重要的作用。单糖增塑膜和多元醇增塑膜具有相似的TS值。然而,单糖增塑膜比多元醇增塑膜具有更高的E值和更低的EM值,这意味着单糖具有更好的淀粉膜增塑效率。当葡萄糖和山梨糖醇增塑的薄膜储存在较高的相对湿度下时,就会发生重结晶。吸附等温线研究表明,所有三个单糖增塑膜和滞后的吸附和解吸曲线相似。 Flory-Huggins模型最适合于淀粉薄膜的实验数据,而BET模型仅适合于数据。

著录项

  • 作者

    Zhang, Yachuan.;

  • 作者单位

    University of Manitoba (Canada).;

  • 授予单位 University of Manitoba (Canada).;
  • 学科 Agriculture Food Science and Technology.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 210 p.
  • 总页数 210
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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