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差热分析法测定化工品、药品纯度 被引量:10

PURITY DETERMINATION OF CHEMICALS & PHARMACEUTICALS BY DSC METHOD
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摘要 研究了差热分析(DSC)法测定化工品、药品纯度的条件,测定的最佳条件为升温速率0.7℃/min,样品量2~3mg,保护气流速20~40mL/min。测定结果的RSD为0.02%,F检验及t检验的结果表明,该方法与容量法无显著差异,该方法简便、快速、准确,适合化工品、药品的定量测定。 The purity determination condition of chemicals and pharmaceuticals by DSC technique was introduced. The optimal testing conditions are: heating ramp being 0.7℃/min, sample weight being 2 - 3 mg and gas flow rate being 20 - 40 mL/min. The experiments yielded good result: there is no significance between DSC and conventional method by F-test and t-test, and RSD is 0.02% . It can be used in the quantative determination of chemicals and pharmaceuticals with its accuracy, convenience and practicality.
出处 《化学分析计量》 CAS 2001年第6期23-24,共2页 Chemical Analysis And Meterage
关键词 差热分析 纯度测定 化工品 药品 differential scanning calorimeter (DSC), purity determination, chemical, pharmaceutical
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参考文献7

  • 1[1]Giron D, et al. Thermal analysis methods for pharmaceutical materials. J of Pharm & Biochemical Analysis, 1989,7(12): 1421
  • 2[2]ASTM E 967 - 92 Standard Practice for Temperature Calibration of Different Scanning Calorimeter and Different Thermal Analyzers
  • 3[3]ASTM E 968 - 83 Standard Practice for Heat Flow Calibration of Different Scanning Calorimeters
  • 4[4]Widmann G, et al. A new program for DSC purity analysis. J of Thermal Analysis, 1991,37:1957
  • 5[5]ASTM E 928 - 85 Standard Test Method for Mol Percent Impurity by Different Scanning Calorimetry
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  • 7[7]Giron D. Place of DSC purity analysis in pharmaceutical development. J of Thermal Analysis, 1995,44: 217

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