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Received April 20, 2007
Accepted April 28, 2007
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2-부텐의 수첨이성화반응 및 증류공정을 통한 고순도 1-부텐의 제조
Synthesis of Pure Butene-1 through Hydro-isomerization of Butene-2 and Distillation
동양대학교 생명화학공학과, 750-711 경북 영주시 풍기읍 교촌동 1 1공주대학교 화학공학부, 314-701 충남 공주시 신관동 182 2SK(주) 대덕기술원, 305-712 대전시 유성구 원촌동 140-1
Department of Chemical Engineering, Dong Yang University, 1, Gyochon-dong, Punggi-eup, Yeongju, Gyeongbuk 750-711, Korea 1Department of Chemical Engineering, Kongju National University, 182, Shinkwan-dong, Gongju, Chungnam 314-701, Korea 2Chemicals R&D Center, SK Corporation, 140-1, Wonchon-dong, Yuseong-gu, Daejeon 305-712, Korea
jkjeon@kongju.ac.kr
Korean Chemical Engineering Research, August 2007, 45(4), 351-355(5), NONE Epub 28 August 2007
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Abstract
C4 잔사유에 포함되어 있는 2-부텐을 부가가치가 더 높은 1-부텐으로 위치 이성화하는 공정의 개발이 필요하다. 본 연구에서는 2-부텐을 1-부텐으로 전환하기 위하여 상업용 Pd/alumina 촉매를 사용하여 수첨이성화반응 실험을 수행하였다. 상업용 Pd 촉매인 LD-265 촉매가 같은 반응조건에서 다른 상업용 촉매들보다 1-부텐 수율이 높았다. 1-부텐의 최적반응조건은 반응온도 75 ℃, 반응압력 150 psig, 2-부텐의 유량 48 cc/h, H2 유량 48 cc/h이었으며, 이 조건하에서 1-부텐의 수율이 5.3%로 최대임을 알 수 있었다. 수첨이성화 반응기와 증류탑으로 구성된 공정의 모사를 수행하였다. 순도 99.0% 이상의 1-부텐을 얻기 위해서 단 효율이 78% 일 때 환류비가 120이고 171 단의 증류탑이 필요한 것으로 나타났다.
It is necessary to convert butene-2 into butene-1 with higher added-values through positional isomerization. In this study, hydro-isomerization of butene-2 with hydrogen over Pd/alumina catalysts was investigated in a fixed bed reactor. The yield of butene-1 over Ld-265 catalyst was higher than that over other catalysts. The yield of butene-1 was highest (5.3%) under the conditions of reaction temperature of 75 ℃, reaction pressure of 150 psig, 2-butene flow rate of 48 cc/h and hydrogen flow rate of 3 cc/min. We conducted simulation for the process composed of a hydroisomerization reactor and a distillation tower. In the case of 78% of tray efficiency, we obtained over 99% pure butene-1 through a distillation tower with 171 steps (R=120).
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References
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Ancillotti F, Forlani O, Jover B, Resofski G, Gati G, Appl. Catal., 67(1), 237 (1990)
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Seo G, Catalysis Surveys from Asia, 9(3), 139 (2005)
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Bradford JR, Drickamer HG, AIChE J., 39, 319 (1943)