共查询到17条相似文献，搜索用时 140 毫秒
1.
2.
两级泡沫分离废水中大豆蛋白的工艺 总被引：2，自引：2，他引：0
为了有效处理高浓度大豆蛋白废水,在研究初始pH值、表观气速和温度特别是在较高温度（60℃）对泡沫分离大豆蛋白废水效果影响的基础上,建立了可同时提高富集比和回收率的两级泡沫分离工艺。在60℃时,对大豆蛋白质量浓度为4.0 g/L的废水泡沫分离,富集比比常温时提高4倍多。两级泡沫分离工艺中,第一级分离在大豆蛋白质量浓度为4.0 g/L,初始pH值为7.0,表观气速0.133 cm/s,60℃下操作,富集比为7.71,残液作为第二级泡沫分离的进料;第二级分离先在20℃,表观气速0.133 cm/s下进行,待塔顶 相似文献
3.
为确定花生叶可溶性蛋白提取最佳工艺,本试验以花生叶为材料,利用碱溶酸沉法提取花生叶可溶性蛋白,分析浸提pH值、料液比及提取时间对蛋白提取率的影响;在单因素试验的基础上,采用Box-Behnken响应面分析法(RSM)优化花生叶可溶性蛋白提取条件,并对所得蛋白进行抗氧化活性分析。结果表明,各影响因素主次顺序为浸提pH值>提取时间>料液比,最佳提取条件为料液比1∶20(w/v)、提取时间40 min、浸提pH值 9.0,以此条件建立的响应面试验回归模型拟合性好(R2=0.992 7),花生叶可溶性蛋白理论提取率为52.8%,实际提取率为54.2%,纯度为63.8%。花生叶可溶性蛋白具有较强的DPPH自由基、超氧阴离子自由基清除能力,以及较好的还原能力。本研究结果为花生叶的开发利用及花生产业链的延长提供了一定的数据支持。 相似文献
4.
酶解法提取黑木耳中胶原蛋白的工艺优化 总被引：1，自引：1，他引：0
为了提高提取黑木耳中胶原蛋白得率,研究黑木耳中胶原蛋白提取工艺路线优化酶法提取的最适条件,采用单因素试验与多元线性回归试验设计相结合的试验方法,经过数据计算统计分析,由回归方程可知,在一定范围内得率与pH值呈正相关,与液料比呈正相关,与酶添加量呈负相关,与酶解时间呈负相关,得出优化工艺参数为:采用胰蛋白酶,酶解pH值为8.0,液料比为52.5:1mL/g,酶添加量为8%,酶解时间为2h,其中在此条件下从黑木耳中提取胶原蛋白得率达到1.091%。研究结果为植物性胶原蛋白制备提供了参考。 相似文献
5.
为进一步提高超声辅助提取黑米黑色素的效果,研究探讨了双频超声协同强化提取的方法。通过对pH值、提取时间、提取温度、液料比、乙醇浓度进行单因素试验,考察各因素对黑色素提取效果的影响,利用正交试验,优化其工艺条件。试验结果表明：各因素对黑米黑色素提取的影响大小依次为：pH＞乙醇浓度＞液料比＞温度＞时间。优化后的提取工艺条件为：pH值为2、超声时间为30?min、提取温度为50℃、液料比为30?mL/g、乙醇浓度为70%。在此条件下,得出平均提取率为6.85%。对比浸渍法、加热回流提取法,超声法提取黑米黑色素具有工艺简单、节省提取时间、溶剂用量少、提取效率高、减少黑色素损失的优点。 相似文献
6.
工艺条件对猪皮提取物质构和微观结构影响的初步研究 总被引：6，自引：1，他引：5
为了给猪皮提取物在肉制品加工中的应用创造条件,采用单因素试验,分别测定不同提取条件(煮沸时间、料液比、pH值、盐浓度)下凝胶质构和微观结构的变化,在此基础上,采用正交试验优化提取条件。单因素试验表明煮沸时间、料液比、提取液pH值对猪皮提取物的质构特性都有显著影响,煮沸时间为60min、料液比为1:5、提取液pH值为5时形成的凝胶最好,盐浓度对质构特性无显著影响。正交试验表明,料液比1:5,盐浓度为3%,煮沸时间60min,pH=6的提取条件下获得的提取物凝胶的质构特性及微观结构最好。 相似文献
7.
大孔吸附树脂分离纯化红小豆多酚工艺及效果 总被引：5，自引：4，他引：1
为开发利用红小豆加工副产物中的生理活性物质,该研究采用大孔树脂吸附法对煮制红小豆水的多酚类物质进行分离纯化,比较了5种不同型号大孔树脂对红小豆多酚的吸附分离效果,从中筛选出HPD 600型树脂作为理想的吸附剂;研究了 HPD 600树脂对红小豆多酚的吸附等温线,结果表明,该吸附等温线与 Langmuir、Freundlich函数曲线的拟合程度非常高,且采用Langmuir模型的拟合效果略优于Freundlich模型。静态和动态吸附、洗脱试验结果表明：样品液浓度、温度、pH值、乙醇浓度、上样流速及洗脱流速等因素均对HPD 600树脂吸附分离红小豆多酚有影响。较理想的工艺参数为：30℃是较适宜的静态吸附温度;保持煮制红小豆水本身的多酚浓度0.96 mg/mL和pH值6.8,上样体积200 mL,上样流速1.0 mL/min进行动态吸附;吸附饱和平衡后,采用50 mL 60%乙醇溶液,以1.5 mL/min的流速进行动态洗脱。依此得到的红小豆多酚纯化液,其总酚含量和总抗氧化能力均有显著提高,约为纯化前的2.2倍。 相似文献
8.
为探寻一种油料蛋白提取方法,该研究以双低冷榨菜籽饼为原料,碱性电解水为溶剂,通过单因素与响应面试验确定了碱性电解水提取冷榨菜籽饼分离蛋白（Alkaline electrolyzed water extracted Rapeseed Protein,ARP）的优化条件,并与相同条件下碱溶酸沉法提取菜籽分离蛋白（Ultrapure water extracted Rapeseed Protein,URP）的结果进行对比。结果表明: 提取工艺各环节因素对菜籽蛋白提取率影响的主次顺序分别为：碱性电解水pH值、温度、料液比、时间;提取优化工艺条件为温度45 ℃、碱性电解水pH值11.5、料液比1:10 g/mL和提取时间60 min,蛋白质提取率为59.34%。与相同条件下碱溶酸沉法相比,碱性电解水提取的菜籽分离蛋白游离巯基和二硫键含量高、表面疏水性强、粒径小、ζ电位绝对值大,同时其提取率、溶解性、持油性、乳化性和起泡性均显著得到改善（P＜0.05）;此外,ARP内源荧光光谱强度更高,二级结构更有序。由此可知,该研究结果为碱性电解水提取冷榨菜籽饼蛋白提供参考,不仅提高了提取率,而且最大程度地减少了对菜籽蛋白结构和功能特性的破坏。 相似文献
9.
条斑紫菜多糖提取工艺的优化 总被引：9，自引：4，他引：9
该文利用二次通用旋转设计对条斑紫菜多糖提取工艺条件中的浸提温度、浸提时间、料液比3因子的最优化组合进行了定量研究，并对建立模型进行了规划求解及试验验证，同时还分析了盐酸脱蛋白的可行性。经试验验证，当料液比为1160∶100(mg/mL)、时间为4.7 h、温度为100℃时多糖得率最高，为(22.22±0.92)%(n=3)与理论计算值(23.34％)基本一致；当料液比为1160∶100(mg/mL)、时间为1.3 h，温度为73.2℃时，多糖纯度最高达(94.60±0.90)%(n=3)，稍低于理论计算值(98.60％)，回归模型可较好地预测多糖的得率和纯度。三氯乙酸和盐酸在pH 2.5时的脱蛋白率分别为73.73%和69.55%，差异不显著，实际生产中可用盐酸替代三氯乙酸进行脱蛋白处理。 相似文献
10.
微波辅助提取黄皮果肉果胶工艺参数优化 总被引：2，自引：1，他引：1
为优化微波辅助提取黄皮果肉中果胶的工艺,采用均匀设计法,考察了微波功率、提取时间、液料比及提取液pH值4个因子对黄皮果胶得率的影响。利用SAS软件对试验数据进行模型拟合和回归分析,确定提取时间和液料比是影响果胶得率的重要因子,并最终获得微波辅助提取黄皮果胶的最优工艺参数为:微波功率600W,提取时间8min,液料比24:1mL/g,提取液pH值2.0。在此条件下果胶得率为3.59%。通过对果胶基本特性的测定分析,该工艺提取的黄皮果胶品质基本符合国家标准,可为黄皮果胶提取的工业化放大提供参考。 相似文献
11.
12.
石榴皮提取物的大孔树脂纯化及其抗氧化性能 总被引：1，自引：0，他引：1
为开发石榴皮资源提供技术支持,从D101、AB-8和DA-2013种大孔吸附树脂中筛选出D101树脂,进一步研究D101对石榴皮提取物中多酚和总黄酮的纯化工艺。所得最佳纯化工艺为:上柱液浓度5mg/mL,pH5,上柱液体积180mL,上柱液流速80mL/h,以60%乙醇溶液为洗脱液,洗脱流速80mL/h,洗脱液体积为100mL。在此条件下,多酚和总黄酮的含量由30.43%和17.12%分别提高到53.55%和35.71%。同时对纯化前后的抗氧化活性进行了比较研究。结果表明,石榴皮提取物经纯化后清除二苯基三硝基苯肼自由基(DPPH·)和抗油脂过氧化能力都强于粗提物。 相似文献
13.
Chen CZ Yan CT Kumar PV Huang JW Jen JF 《Journal of agricultural and food chemistry》2011,59(15):8078-8085
In this study, a simple and novel microdialysis sampling technique incorporating hollow fiber liquid phase microextraction (HF-LPME) coupled online to high-performance liquid chromatography (HPLC) for the one-step sample pretreatment and direct determination of alachlor (2-chloro-2',6'-diethyl-N -(methoxymethyl)acetanilide) and its metabolite 2,6-diethylaniline (2,6-DEA) in microbial culture medium has been developed. A reversed-phase C-18 column was utilized to separate alachlor and 2,6-DEA from other species using an acetonitrile/water mixture (1:1) containing 0.1 M phosphate buffer solution at pH 7.0 as the mobile phase. Detection was carried out with a UV detector operated at 210 nm. Parameters that influenced the enrichment efficiency of online HF-LPME sampling, including the length of the hollow fiber, the perfusion solvent and its flow rate, the pH, and the salt added in sample solution, as well as chromatographic conditions were thoroughly optimized. Under optimal conditions, excellent enrichment efficiency was achieved by the microdialysis of a sample solution (pH 7.0) using hexane as perfusate at the flow rate of 4 μL/min. Detection limits were 72 and 14 ng/mL for alachlor and 2,6-DEA, respectively. The enrichment factors were 403 and 386 (RSD < 5%) for alachlor and 2,6-DEA, respectively, when extraction was performed by using a 40 cm regenerated cellulose hollow fiber and hexane as perfusion solvent at the flow rate of 0.1 μL/min. The proposed method provides a sensitive, flexible, fast, and eco-friendly procedure to enrich and determine alachlor and its metabolite (2,6-DEA) in microbial culture medium. 相似文献
14.
Thorstensen CW Lode O Christiansen AL 《Journal of agricultural and food chemistry》2000,48(12):5829-5833
A rapid solid-phase extraction (SPE) method was developed for the determination of bentazone and the phenoxy acids 2,4-D, dichlorprop, MCPA, and mecoprop in Norwegian environmental water samples. Cartridges with a high-capacity cross-linked polystyrene-based polymer were used for off-line preconcentration. The effects of elution solvent, elution volume, sample volume, sorbent mass, pH, and flow rate on the recoveries of the pesticides were investigated using HPLC. Average recovery of >90% was achieved with 500 mg sorbents using 2 mL of methanol with 5% NH3 as elution solvent. The recoveries were independent of sample pH in the tested range of pH 1-7. Using a sample volume of 200 mL, the limits of determination for the phenoxy acids and bentazone are 0.02 microg/L. Sample volumes up to 2000 mL at a flow rate of 60 mL/min could be handled without any loss of analytes, which makes it possible to lower the limits of determination. The SPE method was compared to a routinely used liquid-liquid extraction method. Three different water matrices spiked at 1.0 and 0.05 microg/L were extracted, and the quantification was performed by GC-MS. Both methods permitted the determination of phenoxy acids and bentazone in distilled water, creek water, and well water down to a level of 0.05 microg/L with recoveries >80% for 200 mL samples. Important advantages of the SPE method compared to the liquid-liquid extraction method were the short extraction times, lack of emulsions, use of disposable equipment, and reduced consumption of organic solvents. 相似文献
15.
van Koningsveld GA Walstra P Gruppen H Wijngaards G van Boekel MA Voragen AG 《Journal of agricultural and food chemistry》2002,50(26):7651-7659
In the present study, foam-forming and -stabilizing properties of potato proteins were studied using whipping and sparging tests. The soluble potato proteins are mainly composed of patatin and protease inhibitors. The whipping tests showed that less foam was formed from untreated patatin than from the protease inhibitors, but patatin foam was much more stable. The foam-forming properties of patatin could be strongly improved by partial unfolding of the protein. Whipping tests, at both low (0.5 mg/mL) and high (10 mg/mL) protein concentration, also indicated that foams made with an ethanol-precipitated protein isolate were more stable than those made with beta-casein and beta-lactoglobulin. More generally, it can be concluded that when proteins are used as a foaming agent, a high concentration is required, because the protein available is inefficiently used. Also, there are several variables that may all, in different ways, affect both foam formation (amount of foam, bubbles size distribution) and foam stability. These variables include the type and concentration of protein, solvent conditions (pH, I), and the method used to make the foam. 相似文献
16.
A high-performance liquid chromatography (HPLC) method for the qualitative and quantitative analysis of allantoin in silk and seed of Zea mays has been developed. Allantoin separation in crude extract was achieved using a C 18 column and phosphate buffer solution (pH 3.0) as a mobile phase at ambient temperature at a flow rate of 1.0 mL/min and detected at 210 nm. The results showed that the amount of allantoin in samples was between 14 and 271 mg/100 g of dry plant material. A comprehensive validation of the method including sensitivity, linearity, repeatability, and recovery was conducted. The calibration curve was linear over the range of 0.2-200 microg/mL with a correlation coefficient of r2>0.999. Limit of detection (LOD, S/N=3) and limit of quantification (LOQ) values of the allantoin were 0.05 and 0.2 microg/mL (1.0 and 4.0 ng) respectively. The relative standard deviation (RSD) value of the repeatability was reported within 1.2%. The average recovery of allantoin added to samples was 100.6% with RSD of 1.5%. 相似文献
17.
提高猪场沼液净化处理效果的氨吹脱控制参数 总被引：7，自引：5，他引：2
针对畜禽养殖场沼气工程沼液氨氮浓度高,碳氮比不足,直接采用传统生化污水处理法效果不佳的问题,该文对氨吹脱工艺降低猪场沼液氨氮浓度参数进行了试验研究,探索了不同初始氨氮浓度、pH值、气液比、温度等参数对氨氮去除的效果,并进一步研究了Ca(OH)2的混凝作用。结果表明:初始氨氮质量浓度分别为500和900mg/L时,氨氮去除率无显著差异。在初始氨氮质量浓度为900mg/L,pH值为10.5,气液比(流量比)2000,沼液温度30℃的运行条件下,氨氮去除率较高为81.84%。在Ca(OH)2投加量为5.0g/L条件下,混凝沉淀效果较好,化学需氧量(COD)、总磷(TP)和PO43-去除率分别为30.13%、97.44%和98.76%,但总硬度提高了106%。该文研究结果为开发沼液深度处理工艺提供了数据。 相似文献