A non-catalytic, supercritical methanol route for effective deacidification of naphthenic acids

被引:18
|
作者
Khan, Muhammad Kashif [1 ]
Insyani, Rizki [2 ]
Lee, Jinkee [1 ]
Yi, Minhoe [3 ,4 ]
Lee, Jae Woo [4 ]
Kim, Jaehoon [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Sch Mech Engn, 2066 Seobu Ro, Suwon 16419, Gyeong Gi Do, South Korea
[2] SKKU Adv Inst Nano Technol SAINT, 2066 Seobu Ro, Suwon 16419, Gyeong Gi Do, South Korea
[3] SK Innovat, 325 Exporo, Daejeon 305712, South Korea
[4] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, 291 Daehak Ro, Daejeon 305701, South Korea
关键词
Naphthenic acids; Total acid number; High acid crudes; Supercritical methanol; Esterification; BIODIESEL FUEL; RAPESEED OIL; IONIC LIQUIDS; FATTY-ACIDS; CRUDE OILS; REMOVAL; REDUCTION; ESTERIFICATION; 2-PROPANOL; ALCOHOLS;
D O I
10.1016/j.fuel.2016.06.023
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
High acid crudes contain large amounts of naphthenic acids (NAs), which lead to severe corrosion in oil refinery equipment and serious environmental problems. The goal of this study is to develop a non catalytic supercritical methanol (scMeOH) route for effective deacidification of NA mixtures and high acid crudes (Laguna and Bachaquero-13). Various reaction parameters, including temperature, pressure, reaction time, and NA-to-methanol ratio, are explored to find effective reaction conditions for reducing the total acid number (TAN) of the mixtures. Almost complete TAN reduction of naphthenic acid (96.9%) is achieved at 400 degrees C, 10 MPa, and 3 h. The reaction in scMeOH at 400 degrees C, 30 MPa and 1 h is effective in the TAN reaction of high acid crudes (93.6-94.0%). The chemical composition of the liquid products obtained under the different reaction conditions, analyzed using gas chromatography-mass spectroscopy, show that esters are the most abundant species, indicating that esterification with scMeOH is the major reaction pathway. The most recalcitrant NA species, which remained after the reaction, are found to be 2-ethy1-2,3,3-trimethyl-butanoic acid and 2,3-dimethy1-2-(1-methylethyl)-butanoic acid. This is attributed to the branched hydrocarbons located near the carboxylic acid groups, which hinder the access of methanol molecules. Crown Copyright (C) 2016 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:650 / 659
页数:10
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