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多酚蛋白复合引起的混浊现象是啤酒,果汁需要着重解决的问题之一。本文探讨了标准曲线法测定啤酒,果汁中混浊活性蛋白的可行性。结果表明,PVP的浓度在0.000~0.100g/L范围时,反应产物的浑浊度与PVP浓度成良好的线性关系。 相似文献
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测定30个不同麦芽样品的总氮、可溶性氮、库值、总酚含量以及对应麦汁敏感蛋白及敏感多酚含量,并对结果进行相关性分析发现,麦汁敏感蛋白含量与麦芽可溶性氮呈显著正相关(r=0.686,p0.01),麦汁敏感多酚含量与麦芽总酚呈显著正相关(r=0.646,p0.01),表明麦芽可溶性氮与总酚指标可初步用于评价麦汁中敏感蛋白与敏感多酚含量;其次,选择麦芽可溶性氮与总酚含量差异较大的加麦Metcalfe与澳麦Gairdner、国麦垦七麦芽,按照不同比例进行搭配并制备麦汁,分析发现搭配前后麦汁敏感蛋白及敏感多酚含量呈线性关系,表明可以有选择的使用不同品种麦芽,按特定比例搭配来控制麦汁中敏感蛋白、敏感多酚含量。本研究为从原料角度预测和控制麦汁和啤酒的胶体稳定性提供了支持。 相似文献
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多酚物质对啤酒稳定性的影响 总被引:6,自引:0,他引:6
陈霞 《广州食品工业科技》2001,17(1):25-27
多酚物质对啤酒稳定性的影响主要表现在它的氧化还原性及与蛋白质结合能力上,啤酒的混浊主要为多酚及氧化产物与蛋白质的聚合物;所以多酚是影响啤酒的非生物稳定性的主要物质之一。另一方面多酚物质又是构成啤酒风味的主要物质,它具有氧化还原性直接影响啤酒的风味稳定性。提出了合理控制多酚物质的手段。 相似文献
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作者对麦汁、后贮酒、清酒、成品的敏感蛋白和敏感多酚进行了跟踪检测,主要目的是为摸清啤酒中敏感蛋白和敏感多酚的实际情况和变化规律,为以后的工艺改进提供数据基础。 相似文献
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引起啤酒、白酒和澄清果汁出现混浊或沉淀的原因很多,最常见的是由蛋白质———多酚的相互作用引起的,但这些饮料一般能稳定存在,并能延缓蛋白质———多酚混浊物形成开始的时间。10多年前已有关于促使蛋白质或多酚成为混浊激活物(HA)方面的报道(Asanoetal,1982;Moll,1987),但近来的研究发现,饮料中两者的比例对混浊的形成数量起着重要的作用(Siebertetal,1996c),这发现使我们能更好地理解一些检测HA种类的分析方法及其稳定的机制。在鉴别HA物质的特性方面,我们已经做子大量的工作(Moll,1987)。啤酒中的… 相似文献
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Analysis of cooling curve to determine the end point of freezing 总被引:1,自引:0,他引:1
M. Shafiur Rahman Nejib Guizani Mohammed Al-Khaseibi Salim Ali Al-Hinai Salha Saleh Al-Maskri Khalid Al-Hamhami 《Food Hydrocolloids》2002,16(6):111
The cooling curve method used for the measurement of freezing point of food is further analyzed to explore whether it can be used to identify the end point of freezing or glass transition. In this method, slope of the cooling curve is determined and plotted as a function of time to identify the end point of freezing (T′m). Initially, the slope is decreased and then reached a minimum value, which is identified as the nucleation of ice. Then the slope is increased until the end point of freezing. The end point of freezing is identified when the slope starts to decrease from its highest value or plateau. Sucrose solutions and starch gels were used to measure its T′m in identifying validity of the proposed method. The measured values of T′m by the proposed method is very close to the literature values. 相似文献
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Citation: IFSCC Magazine, 11 (2008) (2) 139–142 Abstract: Due to the improved performance of modern hair colorants, the high natural variability in hair qualities and the individual influences of manual product applications, colour care effects of cosmetic treatments are very difficult to detect. A new, highly sensitive test method to study the colour fading behaviour of human hair was established for a large variety of cosmetic treatments. This method is based on an automatic multistage application of standard wool tissues combined with automatic colour evaluation by means of CIE L × a × b × measurements (DIN 5033). The delta E values are the main interest because they include all information regarding the L (black vs. white), a (red‐green) and b (blue‐yellow) axes defined in the Hunter Lab colour space. For validation of this new method, different permanent and non‐permanent hair colour shades were applied to undamaged light brown Caucasian hair strands. The hair strands were washed manually stepwise 30 times and the colour loss compared with the results obtained on wool tissues using an automatic application system. For most of the investigated hair colours, a coefficient of determination of r2 > 0.99 was achieved. Modern permanent hair colours show a high resistance to cosmetic treatments. Over 90% of the initial colour result was retained after 30 product applications. Shampoo and conditioner formulations induce different degrees of colour loss in hair. In basic formulas significant influences of single surfactants could be detected. The new method using wool tissues correlates very well with that using manually washed Caucasian hair strands. This automatic method is very time‐effective and offers an excellent reproducibility with a high sensitivity for assessing product influences on artificial hair colours. Keywords: Color fading, color protection, color retention, hair color resistance, hair wash simulation Paper presented at the IFSCC Conference 2007, Amsterdam, The Netherlands 相似文献
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Judges performed over 2000 same-different tests followed by over 2000 A Not-A tests, to distinguish between ‘threshold’ sodium chloride solutions and purified water. Fitting ROC curves to the data indicated that three out of four judges used a τ-strategy for the same-different test. The hypothesis that judges might, with experience, start to categorize the stimuli and switch to a β-strategy was generally not confirmed. On changing to the A Not-A method, half the judges appeared to continue initially to use the τ-strategy. The hypothesis that judges might make comparisons with the preceding stimulus rather than the standard stimulus, because of prior extensive experience with the same-different test, was generally not confirmed. Yet, in all cases there were exceptions. 相似文献
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The sensitivity of the normal picrate method for determination of total cyanide in cassava was increased tenfold using a small 1 cm2 picrate paper, eluted using 0.5 mL instead of 5 mL of water as in the normal method. The absorbance was measured in a 2 mm cuvette in the spectrophotometer. The sensitive method was calibrated against the normal picrate method. The total cyanide content in mg HCN equivalents/kg sample = ppm, is calculated from the absorbance (A) by the equation ppm = A × 45.7 which is applicable from 0.1 to 50 ppm. A new method to determine acetone cyanohydrin was developed based on irreversible denaturation of linamarase in 0.1 M HCl at 30 °C for 1 h. Five gari samples from Mozambique gave a mean total cyanide content of 12 ppm (range 6–15 ppm) and mean acetone cyanohydrin content of 11 ppm (range 5–14 ppm). Acetone cyanohydrin liberates cyanide quantitatively in the human intestine. 相似文献
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Keith R. Martin Christian G. Krueger Gerardo Rodriquez Mark Dreher Jess D. Reed 《Journal of the science of food and agriculture》2009,89(1):157-162
BACKGROUND: The Folin–Ciocalteu method is routinely used to calculate total polyphenol concentrations (TPP) in food products. However, the use of inappropriate standards such as gallic acid (GA) may give inaccurate estimates of TPP content. A method for the production of a pomegranate (Punica granatum L. ‘Wonderful’) standard was developed and validated to avoid this problem. The PPS was produced by solid phase (C18) isolation of polyphenols from POMx powder (a nutritional supplement) and used for TPP analysis. RESULTS: TPP content of POMx was > 90% using PPS, whereas the GA standard underestimated TPP by up to 30%. Compositional analysis confirmed a balance of about 9% non‐polyphenolic compounds. Mass spectrometry analysis corroborated polyphenol composition and confirmed pomegranate‐specific peaks, i.e., punicalagin and punicalin. CONCLUSION: Results support the use of pomegranate‐specific standards to accurately determine TPP. Copyright © 2008 Society of Chemical Industry 相似文献
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目的 利用质控图对水样亚硝酸盐标准曲线的斜率准确性进行判断。方法 运用X-S控制图, 即平均值-标准偏差控制图对曲线的斜率加以监控, 运用Westgard多质控规则对各个点或相邻点进行独立或联合的数据分析, 确定曲线斜率的有效性。结果 通过回收率和相对偏差的对比, 质控图直接观察法能够弥补加标回收法的不足。曲线斜率为0.2249时, 位于警告限与失控限之间, 说明此数据无效, 重新制作曲线。结论 运用质控规则对曲线斜率数据的准确性进行监控, 能起到有效的指导作用。 相似文献
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袜口处标准腿截面曲线形态是研究袜口压力舒适性的前提和基础,也是袜口优化设计的关键.通过三维人体扫描仪对人体内侧脚踝点水平向上6 cm处腿部形态进行扫描,应用MatLab软件,将腿截面曲线按照直角坐标系每5°为1个点等分为72个点,并在此基础上定义点坐标值,将得到的所有腿截面曲线X和Y分别取平均值,得到袜口处标准腿截面曲线72个点坐标.运用SPSS曲线拟合得到袜口处腿截面曲线的二次方程,曲线方程的建立为袜口处压力数学模型的构建提供了基础数据.对袜口处标准腿截面曲线周长进行了求解,结论为男短袜原始袜口围度的改良设计以及袜口面料弹性伸长率的选取提供了理论参考. 相似文献