晶体尺寸控制对甘氨酸的反变换

IF 3.5 3区 化学 Q2 CHEMISTRY, APPLIED Organic Process Research & Development Pub Date : 2025-02-18 DOI:10.1021/acs.oprd.4c00422
Jeongki Kang, Jongwook Park, Jinsoo Kim, Woo-Sik Kim
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引用次数: 0

摘要

根据Ostwald-Freundlich方程,利用溶解度随晶体尺寸减小而增大的特性,提出了稳定型γ-甘氨酸反相转化为亚稳型α-甘氨酸的方法。首先,我们根据甘氨酸的粒度测量其溶解度的变化。γ-甘氨酸块状晶体在10℃时在水中的溶解度为173 g/L,当晶体尺寸减小到0.9 μm左右时,溶解度增加到185 g/L左右。该浓度高于α-甘氨酸体晶的溶解度(180 g/L)。综上所述,γ-甘氨酸在水溶液中可以反转化为α-甘氨酸。在甘氨酸溶液中,用玻璃微珠研磨约2 μm的γ-甘氨酸晶体24 h,使晶体尺寸减小到约0.8 μm。并使溶液浓度高于α-甘氨酸体的溶解度。α-甘氨酸体晶(约110 μm)生长至170 μm。通过这种方法,实现了γ-甘氨酸晶体溶解,α-甘氨酸晶体生长的反相转变。通过显微镜、XRD、ATR-FTIR对上述逆相变过程进行了验证。
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Inverse Transformation of Glycine by Crystal Size Control
This study proposed a method for inverse phase transformation of stable γ-glycine into metastable α-glycine by using the characteristic that solubility increases as crystal size decreases according to the Ostwald–Freundlich equation. First, we measured the change in solubility according to the particle size of glycine. The solubility of γ-glycine bulk crystals at 10 °C in water was 173 g/L, and when the crystal size decreased to about 0.9 μm, the solubility increased to about 185 g/L. This concentration was higher than the solubility of α-glycine bulk crystals, 180 g/L. Based on the above results, γ-glycine can be inverse transformed into α-glycine in aqueous solution. To demonstrate this inverse transformation, in a glycine solution, γ-glycine crystals with a size of about 2 μm were ground with glass beads for 24 h to reduce the crystal size to about 0.8 μm. And the concentration of the solution was made higher than the solubility of α-glycine bulk. α-Glycine bulk crystals (about 110 μm) were placed into this solution and grown to 170 μm. Through this, inverse phase transformation was achieved in which γ-glycine crystals were dissolved and α-glycine crystals grew. The above inverse phase transformation process was confirmed using a microscope, XRD, and ATR–FTIR.
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来源期刊
CiteScore
6.90
自引率
14.70%
发文量
251
审稿时长
2 months
期刊介绍: The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.
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