Optimization of the terpineol synthesis from turpentine oil using p−toluenesulfonic acid catalyst

IF 3.4 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Linh T.T. Nguyen , Nhuan N. Doan , Minh D. Vu , Luong C.T. Pham
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Abstract

P-Toluenesulfonic acid (PTSA) has been identified as a promising homogeneous acid catalyst for the direct hydration of α-pinene (AP), which accounts for approximately 82 % of Vietnam turpentine oil, to produce terpineol. The efficiency of this transformation is influenced by multiple parameters, including the relative molar ratios of reactants, catalyst, and solvent, as well as reaction temperature and time. To support the expansion of this process into industrial applications, this study employed Response Surface Methodology (RSM), a statistical optimization approach, to identify the optimal reaction conditions. In the context of optimized conditions: The molar ratio of AP/PTSA was 1:1, H2O/PTSA was 26:1, and IPA/PTSA was 5:1. The process was conducted at 66 °C for 2.5 h, resulting in a high AP conversion of 98 % and a total terpineol selectivity of 50 %, with α-terpineol accounting for 46 %. Notably, the PTSA catalyst exhibited high levels of activity even after three reuse cycles, thereby substantiating its recyclability. These findings underscore the process as a cost-effective, environmentally friendly, and technically viable route for industrial-scale terpineol production from turpentine oil.

Abstract Image

对甲苯磺酸催化松节油合成松油醇的优化研究
对甲苯磺酸(PTSA)是一种很有前途的均相酸催化剂,用于α-蒎烯(AP)的直接水化生产松油醇,AP约占越南松节油的82%。这种转化的效率受到多种参数的影响,包括反应物、催化剂和溶剂的相对摩尔比,以及反应温度和时间。为了支持该工艺扩展到工业应用,本研究采用响应面法(RSM),一种统计优化方法,以确定最佳反应条件。在优化条件下:AP/PTSA的摩尔比为1:1,H2O/PTSA为26:1,IPA/PTSA为5:1。该工艺在66℃下进行2.5 h, AP转化率高达98%,总松油醇选择性为50%,其中α-松油醇占46%。值得注意的是,PTSA催化剂即使在三次重复使用循环后也表现出高水平的活性,从而证实了其可回收性。这些发现强调了该工艺是一种经济、环保、技术上可行的从松节油中生产工业规模松油醇的方法。
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来源期刊
CiteScore
3.50
自引率
7.70%
发文量
492
审稿时长
3-8 weeks
期刊介绍: The Journal of the Indian Chemical Society publishes original, fundamental, theorical, experimental research work of highest quality in all areas of chemistry, biochemistry, medicinal chemistry, electrochemistry, agrochemistry, chemical engineering and technology, food chemistry, environmental chemistry, etc.
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