淀粉与瓜尔豆胶复配体系糊化及流变特性研究

以玉米淀粉和蜡质玉米淀粉为原料,加入不同配比的瓜尔豆胶,比较两者复配后糊化及流变特性的变化,并采用扫描电镜观察复配体系微观结构。结果表明:添加瓜尔豆胶可使玉米淀粉及蜡质玉米淀粉体系具有更好的增稠性,复配体系表现出更优越的黏弹性。胶体分子与直链淀粉分子间的相互作用是引起玉米淀粉与瓜尔豆胶复配体系流体指数和淀粉成糊温度显著降低,协同作用更为显著的主要原因。微观结构观察表明淀粉与胶体复配体系呈现出更加均一、紧凑的结构。     

香豆胶流变性的研究

研究了香豆胶的流变特性。胶中甘露糖：半乳糖大约为1：1,分子量约为3．12×105。较低浓度时剪切速率范围内剪切速率与粘度无相关性。较高浓度时香豆胶表现剪切变稀现象。由于聚合物水解,粘度随pH的降低而下降。在较高的pH范围,中性聚合物转变为聚电解质,使粘度增加。温度下降,粘度也降低。香豆胶的粘弹性较其它半乳甘露聚糖低,可能是由于较高的半乳糖含量使得内部交联降低,粘度下降。     

直链淀粉含量对玉米淀粉/瓜尔胶复配体系糊化和流变特性的影响

为考察直链淀粉含量对淀粉/瓜尔胶复配体系性质的影响,以不同直链淀粉含量的玉米淀粉(蜡质玉米淀粉、普通玉米淀粉和高直链玉米淀粉)为原料,加入瓜尔胶,研究复配体系的糊化、流变及凝胶特性。结果表明:瓜尔胶与直链淀粉之间的相互作用是引起淀粉复配体系黏度和稠度系数增加、成糊温度和流体指数降低的主要原因。动态流变实验结果表明淀粉中直链淀粉含量不同对复配体系的动态模量的影响也不同。在糊化过程中,随着直链淀粉含量增加,直链淀粉分子与瓜尔胶间的相互作用增强,阻碍了直链淀粉分子间的聚集重排,使得复配体系硬度值减小,3种玉米淀粉形成了质地更为柔软的凝胶。     

玉米淀粉糊流变特性研究

利用AR–500流变仪,研究了不同质量浓度、温度和加热时间条件下玉米淀粉糊的流变特性。结果表明:玉米淀粉糊主要表现为假塑性非牛顿流体,流变特性服从Carreau模型。在同一剪切速率下,黏度随着质量浓度增大而增大,随着温度升高而降低,随着加热时间延长而下降;在同一质量分数条件下,黏度随着剪切速率的增加而呈现先增加后降低的趋势;在同一温度条件下,黏度随着剪切速率的增加而降低。     

直链淀粉含量对玉米淀粉/瓜尔胶复配体系糊化和流变特性的影响

为考察直链淀粉含量对淀粉/瓜尔胶复配体系性质的影响,以不同直链淀粉含量的玉米淀粉(蜡质玉米淀粉、普通玉米淀粉和高直链玉米淀粉)为原料,加入瓜尔胶,研究复配体系的糊化、流变及凝胶特性。结果表明:瓜尔胶与直链淀粉之间的相互作用是引起淀粉复配体系黏度和稠度系数增加、成糊温度和流体指数降低的主要原因。动态流变实验结果表明淀粉中直链淀粉含量不同对复配体系的动态模量的影响也不同。在糊化过程中,随着直链淀粉含量增加,直链淀粉分子与瓜尔胶间的相互作用增强,阻碍了直链淀粉分子间的聚集重排,使得复配体系硬度值减小,3种玉米淀粉形成了质地更为柔软的凝胶。     

瓜尔豆胶对马铃薯淀粉消化性和糊化特性的影响

研究瓜尔豆胶对马铃薯淀粉消化性和糊化特性的影响,采用体外模拟消化性实验测定淀粉的消化性,比较与不同质量比(0:100、1:80、1:40、1:20)的瓜尔豆胶与马铃薯淀粉间糊化特性、热力学特性、结晶结构及微观结构的差异,从而探索瓜尔豆胶对马铃薯淀粉消化性影响的本质原理。研究结果显示:当瓜尔豆胶添加量较低时复配体系经糊化后冷却至37 ℃的体系较易被酶解,抗性淀粉含量低;随着瓜尔豆胶添加量的增大,瓜尔豆胶与淀粉颗粒缠结形成空间位阻从而抑制酶解,复配体系经糊化后冷却至37 ℃的体系不易被酶解,抗性淀粉含量较高。添加瓜尔豆胶增大了马铃薯淀粉的起始糊化温度和峰值温度,提升了马铃薯淀粉的吸热焓,延长糊化过程,增加吸热量。观察复配体系的结晶结构发现加入胶体后复配体系并没有新基团产生,胶体与淀粉间仅为物理作用,同时微观结构观察表明胶体与淀粉作用所形成空间位阻使得淀粉颗粒分布均匀,复配体系呈现出更加均一稳定的结构。     

刺槐豆胶与玉米淀粉混合物流变性分析

为研究非淀粉多糖类胶体对淀粉流变特性的影响,测定5组不同配比刺槐豆胶/玉米淀粉混合物0∶1.2、0.1∶1.1、0.2∶1.0、0.9∶0.3、0.4∶0.8(质量比)的黏弹性。采用Power-Law模型对静态流变学试验数据进行回归拟和,决定系数R~2均在0.99以上,流体指数n1,表明玉米淀粉及两者混合体系属于假塑性流体;随着刺槐豆胶/玉米淀粉混合物质量比的提高,混合体系的稠度系数显著增加,流体指数降低,假塑性增强。当刺槐豆胶/玉米淀粉质量比小于0.3∶0.9(质量比)时,稠度系数增加不再显著。动态流变学试验显示,刺槐豆胶/玉米淀粉质量比大于0.3∶0.9(质量比)时,弹性较大,黏度适中。刺槐豆胶/玉米淀粉质量比为0.4∶0.8(质量比)时,黏度最大,弹性最小,混合体系具有更好的协同增稠效果。     

玉米淀粉与黄原胶复配体系糊化及回生特性的研究

本文研究了玉米淀粉与黄原胶复配体系的糊化和回生特性。RVA糊化实验表明黄原胶降低了玉米淀粉的成糊温度,并随着黄原胶在复配体系中的比例逐渐增加,其复配体系的峰值黏度和终值黏度均显著增加(p<0.05),崩解值和回生值降低(p<0.05)。热稳定性实验表明加入黄原胶后的复配体系在95℃之后的高温下可以较长时间维持体系的黏度,具有良好的热稳定性。凝沉性实验表明黄原胶可以降低玉米淀粉的凝沉作用,当m(玉米淀粉)∶m(黄原胶)为9∶1时复配体系凝沉作用最小,在120h后仍无明显上清液析出。冻融稳定性实验表明黄原胶能抑制复配体系的回生,提高其冻融稳定性。      

瓜尔豆胶对锥栗淀粉糊化和流变学特性的影响

以新鲜锥栗为原料,考察了瓜尔豆胶对锥栗淀粉的糊化特性和流变学特性的影响。结果表明,向锥栗淀粉中添加瓜尔豆胶后,锥栗淀粉糊化溶液的峰值黏度和终值黏度增大,且随瓜尔豆胶添加比例的增加而增大;添加瓜尔豆胶增大了锥栗淀粉的起始糊化温度和峰值糊化温度,提高了锥栗淀粉的吸热焓,使得糊化过程更长,吸热更多。添加瓜尔豆胶后的锥栗淀粉溶液显示为假塑性流体,剪切变稀现象更为明显,具有更大的黏弹性。添加瓜尔豆胶后,混合物形成的凝胶表面空隙中填充物增多,空隙数量减少,且空隙分布更加均匀。     

魔芋胶和玉米淀粉混合物黏弹特性的研究

目的 研究魔芋胶对玉米淀粉黏弹特性的影响。方法 以玉米淀粉为原料, 加入不同比例的魔芋胶, 采用动态流变仪来研究魔芋胶玉米淀粉糊化混合物的黏弹特性。结果 Power-Low模型能够有效地表征魔芋胶玉米淀粉糊化混合物的流变性能。魔芋胶玉米淀粉糊化混合物为假塑性流体, 与单独的玉米淀粉糊相比, 随着魔芋胶的添加量增大, 糊化混合物黏稠性增大, 假塑性增强。随着频率的增大, G?和G?均增大, 损失正切值tan δ＜1, 说明魔芋胶的加入使得糊化混合物具有优越的黏弹性。结论 当魔芋胶/玉米淀粉质量比为0.4:0.8时, 糊化混合物弹性最小, 黏性最大, 糊化混合具有更好的协同增稠作用, 即糊化混合物流体流动特征显著。     

Rheological properties of cereal starch gels and Mesona Blumes gum mixtures

The effect of Mesona Blumes gum (MBG) was examined on steady and dynamic shear of MBG/rice starch and MBG/wheat starch gels. In addition, stress relaxation and creep tests were performed for two types of cereal starch gels. The flow curves of both MBG/starch gels exhibited pseudoplastic behavior at shear rates between 0.01 and 10 s⁻¹, and the data were fitted into the power law model (R² = 0.91–0.98). Dynamic mechanical spectrum showed that all gels were strong gels in frequency between 0.1 and 10 Hz. Stress relaxation data at different strains indicated a strain‐softening phenomenon for both gels. Data were fitted into Maxwell model (R² = 0.91–0.98). Creep curves were conducted at the shear stress 6.4 Pa within linear viscoelastic region of both MBG/starch gels. Data were fitted into Burgers model (R² = 0.91–0.98). Apparent viscosity η, storage moduli G′, equilibrium stress relaxation modulus G_e and zero apparent viscosity η₀ of MBG/rice starch gels decreased in the following order: 6/0>6/0.5>6/0.35>6/0.1 (starch/gum w/w). Whereas η, G′, G_e, and η₀ of MBG/wheat starch gels increased gradually along side the increase of MBG contents. The stress relaxation time λ of MBG/rice starch gels increased in the following order: 6/0<6/0.5<6/0.35<6/0.1 (starch/gum w/w) while λ of MBG/wheat starch gels decreased gradually with the increase of MBG level. The influence of MBG on two examined cereal starch is totally opposite.     

The influence of fenugreek gum and extrusion modified fenugreek gum on bread

Fenugreek gum (extruded and non-extruded) was substituted for wheat flour at 0%, 5% and 10% (w/w) and the rheological effects and breadmaking characteristics were determined. Bread containing fenugreek gum (FG) at 5% and 10% showed volumes and texture comparable with a control bread. Quality was high due to sheeting the dough twice as well as the use of the three-fold-turn puff pastry laminating method during processing of dough, instead of the standard rounding of dough. The three-fold-turn method is believed to have caused a higher incorporation of air into the dough as well as facilitated better distribution and incorporation of the fenugreek gum into bread dough. Extruding FG also improved its solubility in bread. Fenugreek gum (FG) resulted in an increase in dough farinograph water absorption compared with the control, but extruding the gum caused an even greater increase in water absorption when compared with the non-extruded gum. The addition of FG to bread dough caused an increase in G′ and G″. Starch pasting using RVA showed an increase in peak viscosity, final viscosity, breakdown and setback in a dose-related response when compared with a control.     

Preparation of resistant starch from starch–guar gum extrudates and their properties

Mixtures of starch, guar gum and citric acid were extruded at a temperature of 150 °C and screw speed of 180 rpm. Properties of the extrudates such as bulk density, expansion ratio, apparent viscosity and resistant starch content were measured with different concentrations of guar gum. Extrusion with citric acid influenced the physical properties and resistant starch content of the extrudate. Expansion ratios were lower for samples extruded with citric acid, and decreased as starch–gum concentration increased. The apparent viscosity of the extrudate increased with increasing guar gum concentration; however, citric acid at 2.0% concentration was found to lower the viscosity of the extrudate. Resistant starch content increased from 6.23% for extruded starch only to 14.21% for starch–gum extrudate, and further enhanced to 16.19% with the addition of 2.0% citric acid to the starch–gum extrudate. Resistant starch increased with increase of gum concentration and decreased with increase of starch–gum concentration from 7.5% to 12.5%.     

阿拉伯胶对玉米淀粉的共混改性

用阿拉伯胶对玉米淀粉浆料共混改性,使用快速黏度仪(RVA)测定阿拉伯胶-玉米淀粉体系的糊化性能,分析阿拉伯胶对淀粉成膜性能的影响。结果表明,阿拉伯胶会大大降低淀粉糊化的峰值黏度和衰减值,提高淀粉浆膜的断裂强度和断裂伸长,并改善淀粉浆膜的硬脆性。     

酸奶对玉米淀粉流变特性的影响

乳酸菌发酵能够产生淀粉酶。为考察含有活性乳酸菌的酸奶对淀粉黏弾特性的影响,本文以玉米淀粉为原料,分别加入1%（v/v）的蒙牛酸奶、完达山酸奶、伊利酸奶,并在37℃保温1小时;用流变仪研究发酵后玉米淀粉的流变学性质。实验结果表明：剪切流变曲线服从Herschel-Bulkley模型 （R>0.90）。屈服应力τ0、粘度系数k增加,流动指数n减小（n<1）,显示发酵后的玉米淀粉仍然是非牛顿、屈服假塑性流体。震荡流变曲线显示添加酸奶的样品组的贮能模量G''与损耗模量G''均大于空白组、且均随着剪切频率的增大而增大。本项研究首次发现经乳酸菌发酵的玉米淀粉,具有更高的黏弹特性。     

Effect of high-pressure homogenization on microstructure and rheological properties of alkali-treated high-amylose maize starch

The effect of high-pressure homogenization (HPH) on the microstructure, rheological properties, paste clarity, as well as gel retrogradation behavior of alkali-gelatinized high-amylose maize starch (HMS) was investigated. The alkali-treated HMS pastes were subjected to HPH at homogenizing pressures of 25, 50, 75, 100, and 125 MPa. After HPH treatment, the uniformity in the microstructure of HMS pastes was greatly increased. At homogenizing pressures greater than 100 MPa, starch ghost particles were found to completely disappear. The apparent viscosity of the HMS pastes was found to decrease significantly due to the application of HPH. The paste clarity of the HMS pastes increased when HPH treatment was applied. After storing at 4 °C for 7 days, HMS pastes homogenized at 50 and 100 MPa displayed weaker viscoelastic behavior than their corresponding unhomogenized pastes. This indicated that HPH treatment is capable of inhibiting starch retrogradation in gels.