亲水胶体对糯玉米汁稳定性影响

为进一步提高糯玉米汁稳定性,比较研究不同亲水胶体(黄原胶、海藻酸钠、瓜尔豆胶和刺槐豆胶)对糯玉米汁体系稳定系数、离心沉淀率、相对黏度和感官的影响,并探讨糯玉米汁体系的静电稳定性。结果表明：黄原胶具有一定的乳化效果,可以在一定程度上缓解糯玉米汁脂肪圈的形成;海藻酸钠、瓜尔豆胶和刺槐豆胶对糯玉米汁的稳定效果较好,并且随着添加量的增加,体系稳定系数和相对黏度逐渐提高;而黄原胶与海藻酸钠、瓜尔豆胶、刺槐豆胶分别以不同质量比复配时,在黄原胶、刺槐豆胶质量比1:4时,糯玉米汁体系稳定性最佳。     

刺云实胶与黄原胶复配体系质构及流变性研究

将总浓度为1%的刺云实胶(TG)与黄原胶(XTG)按照不同的质量比复配,采用质构仪和流变仪对复配体系的凝胶特性和流变学特性进行测定,通过Carreau模型对流动曲线进行拟合分析,并利用电子扫描显微镜分析复配体系网络形成机理。结果表明:在质构分析中TG与XTG质量比为64时有最大的凝胶强度;在流变分析中TG与XTG质量比为64时呈现最大表观黏度并且在频率扫描和温度扫描中表现出最大的储能模量(G′)。因此,TG与XTG的最佳复配比例为质量比64。在pH为5～10时,最佳复配比例体系的黏度保持相对稳定;当添加盐离子(Na+、Ca2+)后,体系黏度降低,Ca2+降低的趋势更为显著。通过电子扫描显微镜(SEM)分析,表明在TG与XTG之间存在明显的协同增效作用,可形成良好的凝胶网络结构。     

魔芋胶-黄原胶复配体系流变学特性及其凝胶形成动力学分析

为探究魔芋胶与黄原胶2 种食品胶复配使用后的协同作用,以魔芋胶和黄原胶为原料,控制总凝胶质量分 数为1%,以魔芋胶与黄原胶质量比分别为2∶8、4∶6、5∶5、6∶4、8∶2进行复配后,考察复配体系的流变学特性并对 其凝胶形成进行动力学分析。结果表明：魔芋胶-黄原胶复配体系具有假塑性,当魔芋胶的添加比例逐渐增大时, 复配体系黏度系数K增大,流体系数n减小,且复配体系的动态黏弹性质也随着魔芋胶与黄原胶的质量比不同而改 变,当魔芋胶与黄原胶质量比为6∶4时,复配体系的K值达到最大、n值最小,具有最强的假塑性及黏弹性。同时, 魔芋胶与黄原胶的不同质量比对凝胶形成速率有较大影响,当质量比小于6∶4时,凝胶形成显示出较慢的速率,且 形成的凝胶强度较弱;当质量比为6∶4时凝胶形成速率加快,SDRa曲线和G’曲线上升明显,形成的凝胶强度增大, 当质量比继续增加时,凝胶形成速率反而降低。采用阿伦尼乌斯方程对凝胶形成过程中的动力学参数进行拟合,决 定系数均在0.98以上,表现出较高的拟合精度;凝胶形成过程中的活化能在魔芋胶与黄原胶质量比为6∶4时有显著 增加（P＜0.05）,高温段与低温段间的活化能也表现出明显差异。     

黄原胶与几种胶复配对花生乳稳定性的影响

研究了黄原胶分别与刺槐豆胶、瓜尔豆胶、魔芋胶复配对花生乳稳定性的影响,通过分析样品沉淀率、油脂析出率、粘度及高温稳定性观察,结果表明,黄原胶与瓜尔豆胶复配时花生乳稳定性最好,最佳复配比例为黄原胶:瓜尔豆胶=1:2,最佳复配用量为0.05 %.     

槐豆胶与黄原胶复配胶的流变性研究

对槐豆胶、黄原胶及其复配胶的流变性进行了研究。结果表明,槐豆胶和黄原胶有强烈的协效增稠性,槐豆胶与黄原胶复配胶的粘度随着浓度的升高而升高;复配胶为“非牛顿流体”;复配胶溶液的最佳加热温度和加热时间为60℃,加热60min;pH对复配胶的粘度有一定的影响;冻融变化使槐豆胶和黄原胶复配胶的粘度有较大幅度的增加。     

猪屎豆胶与黄原胶复配胶的流变性研究

本实验主要通过测定体系黏度研究了猪屎豆胶与黄原胶复配胶的流变学性质。实验结果表明,猪屎豆种子胶与黄原胶有较强烈的协效性,二者的最佳复配比为6：4;复配胶的黏度随浓度的升高而升高,浓度达到0．4％时开始形成凝胶,浓度达到0．8％时形成坚实的凝胶,浓度为0．7％时的溶液黏度为5367mPa·s;混合胶液为“非牛顿流体”,溶液具有“假塑性”;胶液的最佳加热温度为80℃,最佳加热时间为1h;pH5～9、冻融变化、苯甲酸钠、超声波和微波处理对对其黏度影响较小;复配胶具有良好的耐盐稳定性。     

胶体对悬浮果粒果汁饮料稳定性的影响

研究魔芋胶、刺槐豆胶与黄原胶对悬浮果粒果汁饮料稳定性的影响,结果表明:当魔芋胶、刺槐豆胶与黄原胶以3∶2∶2比例复配,用量为0.06%时,悬浮果粒果汁饮料的稳定性最好,且黏度适中,无明显凝胶现象。     

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。     

刺槐豆胶的流变性研究

对刺槐豆胶的流变性进行了研究。研究结论表明：刺槐豆胶的粘度随浓度的升高而升高,当浓度为2%时,其粘度46.4MPa.s;刺槐豆胶为非牛顿流体,其粘度随切变速度的增加而降低;小于80℃加热时可使刺槐豆胶的粘度增加,60℃为刺槐豆胶的最佳加热温度;冷冻对刺槐豆胶溶液的粘度没有影响,而冷藏可使刺槐豆胶的粘度有所下降;pH对刺槐豆胶溶液的粘度影响不大,即刺槐豆胶在酸性溶液和碱性溶液中较为稳定;刺槐豆胶与黄原胶无协效性。     

黄原胶与阴离子瓜尔胶复配溶液的流变特性研究

配制总质量分数为1%的黄原胶与瓜尔胶复配溶液,两者比例分别为0.1%∶0.9%,0.2%∶0.8%,0.3%∶0.7%,0.4%∶0.6%,0.5%∶0.5%,0.6%∶0.4%,0.7%∶0.3%,0.8%∶0.2%,0.9%∶0.1%。通过稳态流动、应变扫描、频率扫描以及动态黏弹性温度扫描与动态黏度温度扫描,观察复配比例对复配溶液的黏度特性随剪切速率及温度的变化情况,黏弹性随应变、频率及温度的变化情况。黄原胶与瓜尔胶通过分子间缠绕或者分子间次级键的相互作用起到增稠协同作用,说明两者复配有利于零剪切黏度、黏度及黏弹性能的增加。在低剪切区域与低频率区域主要呈现黄原胶的贡献,而在高剪切区域与高频率区则以瓜尔胶起主导作用。对复配溶液的频率扫描中G′大于G″,表现类固态的性质。另外,在5~90℃温度范围,G′G″,复配溶液表现出凝胶状态,呈完善的网络结构;同时,黏度随温度的升高而逐步降低,不存在构象转变温度。     

Viscosity of solutions of xanthan/locust bean gum mixtures

Xanthan and locust bean gums are polysaccharides able to produce aqueous solutions with high viscosity and non‐Newtonian behaviour. When these solutions are mixed a dramatic increase on viscosity is observed, much greater than the combined viscosity of the separated polysaccharide solutions. In this work the influences of different variables on the viscosity of solutions of mixtures of xanthan/locust bean gum have been studied. Total polysaccharide concentration, xanthan and locust bean ratio on mixture and temperature at which the gum was dissolved (dissolution temperature) for both xanthan and locust bean gums have been considered. Under these different operational mixture conditions shear rate and time have also been considered to describe the rheological behaviour of the solutions studied. The high viscosity increase observed in these mixtures is due to the interaction between xanthan gum and locust bean gum molecules. This interaction takes place between the side chains of xanthan and the backbone of the locust bean gum. Both xanthan molecule conformation in solution – tertiary structure – and locust bean gum structure show great influence on the final viscosity of the solution mixtures. Xanthan conformation changes with temperature, going from ordered structures to disordered or chaotic ones. Locust bean gum composition changes with dissolution temperature, showing a dissolved galactose/mannose ratio reduction when temperature increases, ie the smooth regions – zones without galactose radicals – are predominantly dissolved. The highest viscosity was obtained for the solution mixture with a total polysaccharide concentration of 1.5 kg m⁻³ and a xanthan/locust ratio of 2:4 (w/w) and when xanthan gum and locust bean gum were dissolved at 40°C and 80°C, respectively. © 1999 Society of Chemical Industry     

Study of emulsions stabilized with Phaseolus vulgaris or Phaseolus coccineus with the addition of Arabic gum, locust bean gum and xanthan gum

The properties of o/w emulsions stabilized with 1%w/v common bean (Phaseolus vulgaris L.), V or scarlet runner bean (P. coccineus L.), Coc extracted by isoelectric precipitation or ultrafiltration, at pH 7.0 and 5.5, with the addition of Arabic gum, locust bean gum, xanthan gum and a mixture of xanthan gum–locust bean gum (0.1 %w/v and 0.25 %w/v) are studied. The stability of emulsions was evaluated on the basis of oil droplet size, creaming, viscosity and protein adsorption measurements. The addition of Arabic gum, caused an increase in D[4,3] values and a decrease in the amount of protein adsorbed at the interface. The addition of locust bean gum in some emulsions reduced the amount of protein adsorbed. The addition of xanthan and to a less extend of the polysaccharide mixture, promoted a decrease in D[4,3]. So, emulsion stability was affected by the polysaccharide nature. Differences were also observed with respect to the protein nature, the method of its preparation and emulsion's pH. All polysaccharides enhanced the emulsions viscosity with xanthan and xanthan–locust bean gum exhibiting the higher values. V isolates and isoelectricaly precipitated isolates of both V, Coc showed higher viscosity values. The stability was enhanced by the increase of the viscosity of the continuous phase and the creation of a network, which prevents the oil droplets from coalescence.     

葫芦巴胶溶液流变特性研究

通过测定和分析浓度、剪切力、温度、pH和冻融等变化对葫芦巴胶溶液表观粘度的影响及与黄原胶等食品胶的协效性,对葫芦巴胶溶液的流变性进行了研究。研究结果表明:冷水溶和热水溶葫芦巴胶溶液的表观粘度都随浓度的升高而呈指数规律的上升;葫芦巴胶溶液为非牛顿流体,其剪切稀化具有瞬时恢复性;随着温度的升高,葫芦巴胶溶液的表观粘度呈半对数规律下降;且溶液具有很强的耐热性;葫芦巴胶溶液在酸性和碱性条件下较为稳定;冻融处理可使葫芦巴胶溶液的表观粘度下降;葫芦巴胶与黄原胶、海藻酸钠有一定的协效性,但其协效性较低,而与CMC却有很强的相互增效的协同效应。     

Effects of gelatinisation level, gum and transglutaminase on the quality characteristics of rice noodle

The aim of the present study was to investigate the effects of gelatinisation level, gum (locust bean gum, xanthan gum, 3%) and/or transglutaminase (TG, 0.5%) on quality characteristics of rice noodle. In order to improve the dough forming ability, rice flour was gelatinised at levels of 15%, 20%, 25% and 30%. Noodle samples were evaluated in terms of cooking loss, total organic matter (TOM), water absorption, swelling volume, maximum force, colour, sensory properties, pasting properties. Noodle sample with a gelatinisation level of 25% had better cooking and sensory properties. Gum and/or TG were added to this noodle formula. The noodle samples including xanthan gum had better cooking and sensory properties. TG caused a significant decrease in TOM. The samples including locust bean gum had significantly higher maximum force values. Xanthan gum caused decreases in some Rapid ViscoAnalyzer viscosity values of the noodle samples, while locust bean gum caused increases.     

Synergistic interaction of xanthan gum with glucomannans and galactomannans

Xanthan gum forms thermoreversible gels when mixed with konjac mannan or locust bean gum. The stronger gels are formed with konjac mannan and the maximum gel strength for the mixed systems in the absence of electrolyte occurs at a xanthan-konjac mannan or xanthan-locust bean gum mixing ratio of about 1:1. In the presence of 0.04 mol/dm³ NaCl the optimum mixing ratio is unchanged for xanthan-locust bean gum blends but changes to about 2:1 for xanthan-konjac mannan blends. These observations support differential scanning calorimetric data which are able to monitor both gelation and the conformational transition of the xanthan molecules and indicates that (i) in the absence of electrolyte konjac mannan interacts with disordered xanthan chains whilst in the presence of 0.04 mol/dm³ NaCl it interacts with ordered xanthan chains, and (ii) locust bean gum interacts with ordered xanthan chains both in the presence and absence of electrolyte.     

黄原胶对莲藕淀粉糊化性质及流变与质构特性的影响

为探究亲水性胶体对淀粉性质的影响,将不同比例的黄原胶添加到莲藕淀粉中,研究两者复配后莲藕淀粉的糊化、流变、质构特性及微观结构的变化。结果表明：黄原胶提高了淀粉糊终值黏度、糊化峰值时间并降低淀粉的崩解值和回生值,复配体系有更好的热稳定性和抗老化性。添加不同比例的黄原胶使莲藕淀粉糊的剪切应力不同程度降低,稠度系数K增大,流体指数n降低,加入黄原胶后的淀粉糊仍为假塑性流体,但是具有更好的增稠作用;加入黄原胶提高了淀粉的贮能模量、损耗模量,降低了损耗角正切值tanδ,体系的黏弹性和稳定性增强,其中莲藕淀粉与黄原胶配比为8.0∶2.0（g/g）的复配体系增稠效果、黏弹性、稳定性最好。复配体系的硬度、内聚性、黏着性、咀嚼性降低,弹性略有增大,添加黄原胶形成的凝胶质地更柔软。扫描电子显微镜观察到添加黄原胶后淀粉内部形成更加均匀稳定的结构。     

食品增稠剂瓜儿豆胶性质及复配性的研究

本文对瓜尔豆胶的流变性,浓度、温度、pH值、电介质对粘度的影响,与黄原胶、卡拉胶复后粘度变化进行了初步研究。结果表明,低浓度瓜儿豆胶属非牛顿流体中假塑性流体,其粘度随浓度升高而上升,随温度升高而下降,几乎不受pH值影响,对NaCl和低浓度Ca~(2+),Al~(3+)有良好兼容性,与卡拉胶复配无增效作用,而与黄原胶复配增效显著,复配最佳比例为瓜儿豆胶:黄原胶=0.6:0.4     

Rheological interactions between Lallemantia royleana seed extract and selected food hydrocolloids

BACKGROUND: Lallemantia royleana (Balangu) is a mucilaginous endemic plant which is grown in different regions of world. The flow behaviour of Balangu seed extract (BSE) and its mixture with xanthan, guar and locust bean gums at 1:3, 1:1 and 3:1 ratios, in addition to control samples (0% BSE), were evaluated. To describe the rheological properties of samples, the power law model was fitted on apparent viscosity–shear rate data. To evaluate the interaction between BSE and selected hydrocolloids in dilute solutions, the relative viscosity was also investigated. RESULTS: There was no significant difference between the consistency coefficient of guar and locust bean solutions and their blends substituted with 250 g kg^?1 BSE. The BSE–xanthan mixture at 1:3 and 1:1 ratios had consistency index equal to xanthan solution. BSE–locust bean gum at all ratios, BSE–xanthan at 1:3 ratio and BSE–guar gum at 1:1 and 3:1 ratios indicated relative viscosity lower than values calculated assuming no interaction. The intrinsic viscosity value of BSE was determined 3.50 dL g^?1. CONCLUSION: The apparent viscosities of BSE, selected hydrocolloids and their blends were the same at a shear rate of 293 s^?1 and the commercial gums can be substituted by 250 g kg^?1 and 500 g kg^?1 BSE. Copyright © 2011 Society of Chemical Industry