Methods for Screening Cloud Point Temperatures

被引:10
作者
Pincemaille, J. [1 ,2 ]
Banc, A. [1 ]
Chauveau, E. [1 ]
Fromental, J. -M. [1 ]
Ramos, L. [1 ]
Morel, M. -H. [2 ]
Menut, P. [2 ,3 ]
机构
[1] Univ Montpellier, CNRS, Lab Charles Coulomb L2C, Montpellier, France
[2] Univ Montpellier, Montpellier SupAgro, INRA, CIRAD,UMR IATE, 2 Pl Pierre Viala, F-34070 Montpellier, France
[3] Univ Paris Saclay, INRA, AgroParisTech, Ingn Proc Aliments, F-91300 Massy, France
关键词
Phase diagram; Cloud point; Liquid-liquid phase separation; Triton TX-114; Wheat gluten; Microplate; LIQUID-PHASE-SEPARATION; DIFFERENTIAL SCANNING CALORIMETRY; NONIONIC MICELLAR-SOLUTIONS; SALT-WATER SYSTEMS; LYSOZYME SOLUTIONS; AQUEOUS-SOLUTIONS; TRITON X-114; PROTEIN; SOLUBILITY; AGGREGATION;
D O I
10.1007/s11483-018-9548-1
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A novel and simple method for the measurement of cloud point temperatures of solutions is presented. Cloud point determination, which is currently used to establish the phase diagrams of protein solutions, is indicative of proteins interactions and constitutes a useful tool for food products engineering. We describe a novel experimental setup that allows screening of a large number of physical-chemical conditions in one measurement and the determination of cloud point temperatures both above and below ambient temperature. We use a simple method to avoid solvent evaporation and condensation, so that the set-up can be used for solutions prepared with a volatile solvent. We present the operating parameter range and the precision of the measurement. The optical properties of the system are calibrated with solutions of known transmittance, and the determination of cloud point temperatures is validated on a standard non-ionic surfactant solution. Finally, we demonstrate the efficiency of the method by determining the phase diagram of a wheat protein extract, soluble in a water/ethanol mixture. Complemented with differential scanning calorimetry measurements, the liquid-liquid phase transition can be determined up to a protein concentration of 250g/L, a range inaccessible with conventional methods for this protein extract.
引用
收藏
页码:422 / 431
页数:10
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