棕油酸蒸的两步化过程使用浸泡与超声波相结合:过程优化和可重复使用的固体酸催化剂
Jarernporn Thawornprasert1, Krit Somnuk1
1Department of Mechanical and Mechatronics Engineering, Faculty of Engineering, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand.
ACS omega
|January 1, 2025
概括
高强度超声波和Amberlyst-15催化剂有效地将棕油脂酸蒸中的自由脂肪酸转化为甲基. 这种可持续的方法实现了高纯度,证明了生物柴油生产的催化剂可重复使用性.
科学领域:
- 化学工程是化学工程的重要组成部分.
- 可持续化学 可持续化学
- 催化剂是一种催化剂.
背景情况:
- 棕脂肪酸蒸 (PFAD) 是一种富含自由脂肪酸 (FFAs) 的副产品.
- 将FFF转化为甲基 (ME) 对于生物柴油生产至关重要.
- 与同质催化剂相比,异质催化剂提供了环境效益和可重复使用性.
研究的目的:
- 通过超声波和异质酸催化剂,优化PFAD中FFF的化到ME.
- 调查Amberlyst-15在生物柴油生产中的效率和可重复使用性.
- 为了确定最大限度地提高ME纯度的最佳反应条件.
主要方法:
- 高强度超声波 (1000 W,18 kHz) 应用于PFAD的化.
- 在这个过程中使用了一种异质酸催化剂Amberlyst-15.
- 反应参数包括甲醇含量,催化剂负载,浸泡时间和超声波时间,以优化ME纯度而变化.
主要成果:
- 在最佳条件下,ME纯度达到89.44%的重量级.
- 最佳条件:36.73重量%的甲醇,60重量%的Amberlyst-15,浸泡130分钟,在60°C下505秒的超声波.
- 回收的Amberlyst-15至少在两个循环中证明了可重复使用性,达到超过80%的ME纯度.
结论:
- 用Amberlyst-15进行超声波辅助化是一种有效的方法,可以降低PFAD中的FFA含量.
- 不同质的催化剂Amberlyst-15可重复使用,为生物柴油生产提供一种可持续的方法.
- 优化条件显著提高甲基产量和纯度.
相关概念视频
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
17.7K
The Fischer esterification reaction was developed by the German chemist Emil Fischer in 1895. It is a condensation reaction between carboxylic acids and alcohols in an acidic medium to give esters and water.
17.7K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
7.6K
Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
7.6K
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
2.6K
Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
2.6K
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
3.3K
Malonic ester synthesis is a method to obtain α substituted carboxylic acids from ꞵ-diesters such as diethyl malonate and alkyl halides.
3.3K
Acid-Catalyzed Dehydration of Alcohols to Alkenes
18.8K
In a dehydration reaction, a hydroxyl group in an alcohol is eliminated along with the hydrogen from an adjacent carbon. Here, the products are an alkene and a molecule of water. Dehydration of alcohols is generally achieved by heating in the presence of an acid catalyst. While the dehydration of primary alcohols requires high temperatures and acid concentrations, secondary and tertiary alcohols can lose a water molecule under relatively mild conditions.
18.8K
Esters to β-Ketoesters: Claisen Condensation Mechanism
3.5K
Regular Claisen condensation involves the synthesis of β-ketoesters by combining identical ester molecules bearing two α hydrogens in the presence of an alkoxide base. The reaction commences with the deprotonation of the acidic α hydrogen by the base to form a resonance stabilized ester enolate. This nucleophilic ion then attacks the carbonyl center of another ester molecule to generate a tetrahedral alkoxide intermediate. Next, the expulsion of the alkoxide group from the...
3.5K


