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Application of Differential Scanning Calorimetry (DSC) and Modulated Differential Scanning Calorimetry (MDSC) in Food and Drug Industries

机译:差示扫描量热法(DSC)和调制式差示扫描量热法(MDSC)在食品和药物工业中的应用

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摘要

Phase transition issues in the field of foods and drugs have significantly influenced these industries and consequently attracted the attention of scientists and engineers. The study of thermodynamic parameters such as the glass transition temperature (Tg), melting temperature (Tm), crystallization temperature (Tc), enthalpy (H), and heat capacity (Cp) may provide important information that can be used in the development of new products and improvement of those already in the market. The techniques most commonly employed for characterizing phase transitions are thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), thermomechanical analysis (TMA), and differential scanning calorimetry (DSC). Among these techniques, DSC is preferred because it allows the detection of transitions in a wide range of temperatures (−90 to 550 °C) and ease in the quantitative and qualitative analysis of the transitions. However, the standard DSC still presents some limitations that may reduce the accuracy and precision of measurements. The modulated differential scanning calorimetry (MDSC) has overcome some of these issues by employing sinusoidally modulated heating rates, which are used to determine the heat capacity. Another variant of the MDSC is the supercooling MDSC (SMDSC). SMDSC allows the detection of more complex thermal events such as solid–solid (Ts-s) transitions, liquid–liquid (Tl-l) transitions, and vitrification and devitrification temperatures (Tv and Tdv, respectively), which are typically found at the supercooling temperatures (Tco). The main advantage of MDSC relies on the accurate detection of complex transitions and the possibility of distinguishing reversible events (dependent on the heat capacity) from non-reversible events (dependent on kinetics).
机译:食品和药品领域的相变问题对这些行业产生了重大影响,因此引起了科学家和工程师的关注。对诸如玻璃化转变温度(Tg),熔融温度(Tm),结晶温度(Tc),焓(H)和热容(Cp)等热力学参数的研究可能会提供重要的信息,可用于开发C.新产品和已有产品的改进。表征相变最常用的技术是热重分析(TGA),动态力学分析(DMA),热机械分析(TMA)和差示扫描量热法(DSC)。在这些技术中,DSC是优选的,因为它允许检测温度范围很广(-90至550°C)的转变,并且易于进行转变的定量和定性分析。但是,标准DSC仍然存在一些限制,可能会降低测量的准确性和精确度。调制差示扫描量热法(MDSC)通过采用正弦调制加热速率(已用于确定热容量)克服了其中一些问题。 MDSC的另一个变体是过冷MDSC(SMDSC)。 SMDSC可以检测更复杂的热事件,例如固体-固体(Ts-s)转变,液体-液体(Tl-1)转变以及玻璃化和失透温度(分别为Tv和Tdv),通常在过冷温度(Tco)。 MDSC的主要优势在于对复杂转变的准确检测以及将可逆事件(取决于热容量)与不可逆事件(取决于动力学)区分开的可能性。

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