環己醇為目前高分子工業中大量被用做製造尼龍前驅物之原料,但現今工業使用之製程大部分有其安全性缺點,日本Asahi公司使用之一步水合反應製程雖改善安全性,但卻遭遇反應速率低之問題,且多操作單元步驟也使得經濟效益較低。本研究將以Asahi製程之一步水合反應整合至反應蒸餾系統為主題,探討熱力學性質對於該系統之影響,其中汽液液分相之三相共存為本系統之特點,並提出含雜質與不含雜質進料之反應蒸餾塔架構組態,針對最佳化設計找到合適的動態控制架構。第二部分為研究Steyer等人於2007年提出之兩步反應生產環己醇程序,並以Katariya等人於2009年提出之兩步反應系統架構為基礎,探討各設計變數於系統之影響;最後將討論整合性架構之可行性,其為包含兩反應段之單一反應蒸餾塔,此為首次提出之架構概念。
In the industrial market, Nylon 6, 6 is an important product and its production rate has reached 1.1 million tons per year by 1999. On the other hand, cyclohexanol has been used as a precursor in the synthesis of intermediates of Nylon 6, 6, i.e. the adipic acid and ε-caprolactam. An “Asahi process” to produce cyclohexanol from benzene by consecutive hydrogenation and one-step hydration steps has been commercialized since 1986. However, the one-step hydration step suffering from very low reaction rate and conversion is the bottleneck in the process. As a result, it is desirable to enhance this hydration step for better production. In this thesis, it is aimed to study the design and control of such a hydration step by employing reactive distillation. Moreover, the possibility of using reactive distillation in alternative two-step reactions is also studied in this thesis and a novel configuration, a two reaction zone in one reactive distillation column, is proposed.