热挤压法制备乳清蛋白浓缩物:蛋白质浓度及其他参数的影响

M. Hossain, Alex, E. Krah, O. Hensel, M. Diakité
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引用次数: 5

摘要

微颗粒化受热挤压过程中诸多因素的影响,包括工艺参数、系统参数以及产品性能。本研究的主要目的是研究蛋白浓度(c蛋白)和工艺参数对乳清蛋白热挤压工艺微颗粒化的影响。在挤压过程中,用去矿化水分别达到所需c蛋白的20、25、30和35%。实验采用旋转双螺杆挤出机(ZSE18HP), L/D比为40:1,最高筒体温度为90℃。采用激光衍射法测定微颗粒乳清蛋白(MWPs)的粒径,采用弗劳恩霍夫近似法计算粒径分布。所有挤压样品的颜色均采用CIE L*a*b*系统测定。此外,粒子的微观性质是确定使用数码显微镜与高倍率透镜。采用SPSS软件进行统计分析和数据拟合。蛋白浓度对微颗粒乳清蛋白的粒径分布有显著影响(p<0.001)。c蛋白含量提高30%,MWPs的粒径减小。另一方面,螺杆转速的增加使颗粒尺寸减小。然而,35%的c蛋白和200转/分的转速给了我们相反的结果。在螺杆转速400 ~ 600 rpm和800 ~ 1000 rpm范围内,分别观察到d50≤5µm和d50≤3µm的颗粒。在粒度分布方面,挤出机的螺杆转速也具有统计学意义(p<0.001)。综上所述,在所谓的微颗粒化过程中,粒径分布可以通过操纵c蛋白以及挤出机的螺杆转速来控制。
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Microparticulation of Whey Protein Concentrates using the Hot Extrusion Process: The Influence of Protein Concentrations and Other Parameters
Microparticulation is influenced by many factors of the hot extrusion process, including process and system parameters as well as product properties. The key aim of this study was to investigate the influence of protein concentrations (Cprotein) and process parameters on microparticulation of whey protein using the hot extrusion process. During the extrusion process, demineralized water was used to reach the desired Cprotein of 20, 25, 30 and 35% respectively. The experiments were carried out using a corotating twin-screw extruder (ZSE18HP) with an L/D ratio of 40:1 at 90°C as the maximum barrel temperature. The particle size of the microparticulate whey proteins (MWPs) was measured using laser diffractometry, and particle size distributions were calculated by Fraunhofer approximation. The colors of all extruded samples were determined using the CIE L*a*b* system. Additionally, the microscopic properties of particles were determined using a digital microscope with a high-magnification lens. The statistical analysis and data fitting were done using SPSS. Protein concentrations and showed a significant (p<0.001) influence on the particle size distribution of microparticulated whey proteins. The particle sizes of MWPs declined by raising the Cprotein up by 30%. On the other hand, the increase of screw speeds caused the particle sizes to decrease. However, 35% of Cprotein and a screw speed of 200 rpm gave us the opposite results. The particles that were d50 ≤ 5 µm and d50 ≤ 3 µm in size were observed from the screw speed range of 400 rpm to 600 rpm and 800 to 1000 rpm respectively. In terms of particle size distributions, the screw speeds of the extruder were also statistically significant (p<0.001). In conclusion, the particle size distributions in the so-called microparticulation process can be controlled through the manipulation of the Cprotein as well as the screw speed of the extruder.
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