scholarly journals Synthesis, Characterization and Optimization of Oleyl Oleate Wax Ester Using Ionic Liquid Catalysts

2021 ◽  
Vol 21 (3) ◽  
pp. 659
Author(s):  
Naowara Al-Arafi ◽  
Nadia Salih ◽  
Jumat Salimon
Keyword(s):  
Ionic Liquid ◽  
Oleic Acid ◽  
Oleyl Alcohol ◽  
Wax Ester ◽  
Esterification Reaction ◽  
Reaction Conditions ◽  
Brønsted Acidic Ionic Liquid ◽  
Acidic Ionic Liquids ◽  
Percentage Yield ◽  
Oleyl Oleate

In this work, the synthesis of oleyl oleate wax ester using Brønsted acidic ionic liquid catalysts was carried out. Confirmation of oleyl oleate molecular structure has been performed using FTIR, NMR, and ESI-MS spectroscopies. The ability of ionic liquid catalysts for catalyzing the esterification reaction of oleic acid and oleyl alcohol to produce oleyl oleate was optimized. The ionic liquid catalyst ([NMP][CH3SO3]) was found to be the best catalyst for the esterification reaction of oleic acid and oleyl alcohol compared with the other acidic ionic liquids studied. The optimal reaction conditions were determined at a reaction time of 8 h; oleic acid to oleyl alcohol mole ratio of 1:1; ([NMP][CH3SO3]) with 9.9 wt.%; and reaction temperature of 90 °C. Under these conditions, the percentage yield of oleyl oleate wax ester was 86%.

scholarly journals Production of Oleic Acid Based Wax Ester Using Acidic Homogeneous Catalysts

2012 ◽  
Vol 9 (1) ◽  
pp. 99-106 ◽  
Author(s):  
Naowara Al-Arafi ◽  
Jumat Salimon
Keyword(s):  
Oleic Acid ◽  
Oleyl Alcohol ◽  
Specific Activity ◽  
Viscosity Index ◽  
Molar Ratio ◽  
Wax Ester ◽  
Esterification Reaction ◽  
Percentage Yield ◽  
Optimum Reaction ◽  
Oleyl Oleate

Four homogeneous acidic catalysts were tested for their ability to catalyze the esterification reaction of oleic acid and oleyl alcohol to produce oleyl oleate, a wax ester. Sulfuric acid showed relatively higher specific activity. Various reaction parameters were optimised to obtain high percentage yield of oleyl oleate. The optimum condition to produce oeyl oleate was reaction time; 5 h, temperture; 90°C, amount of sulforic acid 0.15 g and molar ratio of oleyl alcohol to oleic acid; 1:1. Percentage yield of wax ester obtained at these optimum reaction conditions was 93.88. Disappearance of carboxylic acid (C=O) peak has confirmed by FTIR with appearance of ester (C=O) peak at 1739 cm−1.1H NMR spectra analyses confirmed the result of oleyl oleate with appearance of ester (-CH2OCOR) at 4.02 ppm and also the13C-NMR confirmed the result with appearance of ester (C=O) peak at 173.2 ppm. The low-temperture behavior of compound synthesized was determined through its pour point (PP), viscosity index (VI) and flash point (FP) values. The results showed that oleyl oleate exhibited the most favorable low-temperture performance of PP, VI and FP with −31°C, 197.5 and 320°C respectively. This is due to increase of the molacular weight thus improve the low temperture property significantly.

Brønsted acidic ionic liquid-catalyzed dehydrative formation of isosorbide from sorbitol: introduction of a continuous process

2017 ◽  
Vol 7 (10) ◽  
pp. 2065-2073 ◽  
Author(s):  
Jie Deng ◽  
Bao-Hua Xu ◽  
Yao-Feng Wang ◽  
Xian-En Mo ◽  
Rui Zhang ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Continuous Process ◽  
Efficient Synthesis ◽  
Acidic Ionic Liquid ◽  
Highly Efficient ◽  
Brønsted Acidic Ionic Liquid ◽  
Acidic Ionic Liquids ◽  
First Time

A highly efficient synthesis of isosorbide from sorbitol was developed using Brønsted acidic ionic liquids (BILs) as the catalyst for the first time.

scholarly journals Mild and Efficient Tunable Brønsted Acidic Ionic Liquid Catalyzed O-Acetylation and O-Trimethylsilylation with Trimethylsilyl Acetate (TMSOAc) and Hexamethyldisilazane (HMDS)

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 825
Author(s):  
Amit Ravindra Pantawane ◽  
Mayur Thul ◽  
Yi-Jyun Lin ◽  
Michelle Lin ◽  
Wesley Lin ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Room Temperature ◽  
Visible Spectroscopy ◽  
Acidic Ionic Liquid ◽  
Post Process ◽  
Brønsted Acidic Ionic Liquid ◽  
Acidic Ionic Liquids ◽  
Uv Visible ◽  
Work Up

This report discloses a mild and efficient O-acetylation using easily accessible TMSOAc as a novel acetyl reagent and O-trimethylsilylation using HMDS for various alcohols catalyzed by tunable Brønsted acidic ionic liquids (TBAILs). Imidazolium-based TBAILs were prepared by a two-step atom-economic reaction and acidities measured by using UV-visible spectroscopy. Both protections for alcohols were accomplished at room temperature with good to excellent yields, while the products and TBAILs were separated by simple work-up for O-silylation and column chromatography for O-acetylation. Notably, with the simple post-process, TBAILs catalyst in this solvent free method easily recovered and recycled several times without significant degradation.

scholarly journals Two-Stage Conversion of High Free Fatty AcidJatropha curcasOil to Biodiesel Using Brønsted Acidic Ionic Liquid and KOH as Catalysts

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Subrata Das ◽  
Ashim Jyoti Thakur ◽  
Dhanapati Deka
Keyword(s):  
Ionic Liquid ◽  
Molar Ratio ◽  
Reaction Conditions ◽  
Two Stage ◽  
Second Stage ◽  
Stage Conversion ◽  
Acidic Ionic Liquid ◽  
Brønsted Acidic Ionic Liquid ◽  
Optimum Reaction ◽  
Stage Process

Biodiesel was produced from high free fatty acid (FFA)Jatropha curcasoil (JCO) by two-stage process in which esterification was performed by Brønsted acidic ionic liquid 1-(1-butylsulfonic)-3-methylimidazolium chloride ([BSMIM]Cl) followed by KOH catalyzed transesterification. Maximum FFA conversion of 93.9% was achieved and it reduced from 8.15 wt% to 0.49 wt% under the optimum reaction conditions of methanol oil molar ratio 12 : 1 and 10 wt% of ionic liquid catalyst at 70°C in 6 h. The ionic liquid catalyst was reusable up to four times of consecutive runs under the optimum reaction conditions. At the second stage, the esterified JCO was transesterified by using 1.3 wt% KOH and methanol oil molar ratio of 6 : 1 in 20 min at 64°C. The yield of the final biodiesel was found to be 98.6% as analyzed by NMR spectroscopy. Chemical composition of the final biodiesel was also determined by GC-MS analysis.

Understanding the role of hydrogen bonding in Brønsted acidic ionic liquid-catalyzed transesterification: a combined theoretical and experimental investigation

2016 ◽  
Vol 18 (48) ◽  
pp. 32723-32734 ◽  
Author(s):  
Kaixin Li ◽  
Yibo Yan ◽  
Jun Zhao ◽  
Junxi Lei ◽  
Xinli Jia ◽  
...  
Keyword(s):  
Experimental Investigation ◽  
Ionic Liquid ◽  
Hydrogen Bonding ◽  
Catalytic Activity ◽  
Ionic Liquids ◽  
Acidic Ionic Liquid ◽  
Brønsted Acidic Ionic Liquid ◽  
Acidic Ionic Liquids ◽  
Hydrogen Bonding Networks

The intra- and inter-hydrogen bonding networks that govern the catalytic activity of Brønsted acidic ionic liquids were identified.

scholarly journals Group 13 Lewis Acid Catalyzed Synthesis of Cu2O Nanocrystals via Hydroxide Transmetallation

2021 ◽  
Author(s):  
Noah Gibson ◽  
Alexandria R. C. Bredar ◽  
Byron Farnum
Keyword(s):  
Oleyl Alcohol ◽  
Copper Ions ◽  
Colloidal Synthesis ◽  
Esterification Reaction ◽  
Group 13 ◽  
Oleyl Oleate ◽  
Acid Catalyzed ◽  
Uv Visible ◽  
Continuous Injection ◽  
Injection Procedure

The colloidal synthesis of metal oxide nanocrystals (NCs) in oleyl alcohol requires the metal to catalyze an esterification reaction with oleic acid to produce oleyl oleate ester and M-OH monomers, which then condense to form MxOy solids. Here we show that the synthesis of Cu2O NCs by this method is limited by the catalytic ability of copper to drive esterification and thus produce Cu+ -OH monomers. However, inclusion of 1-15 mol% of a group 13 cation (Al3+, Ga3+ , or In3+) results in increased yields for the consumption of copper ions toward Cu2O formation and exhibits size/morphology control based on the nature of M3+ . Using a continuous-injection procedure where the copper precursor (Cu2+ -oleate) and catalyst (M3+ -oleate) are injected into oleyl alcohol at a controlled rate, we are able to monitor the reactivity of the precursor and M3+ catalyst using UV-visible and FTIR absorbance spectroscopies. These time-dependent measurements clearly show that M3+ catalysts drive esterification to produce M3+ -OH species, which then undergo transmetallation of hydroxide ligands to generate Cu+ -OH monomers required for Cu2O condensation. Ga3+ is found to be the “goldilocks” catalyst, producing NCs with the smallest size and a distinct cubic morphology not observed for any other group 13 metal. This is believed to be due to rapid transmetallation kinetics between Ga3+ -OH and Cu + -oleate. These studies introduce a new mechanism for the synthesis of metal oxides where inherent catalysis by the parent metal (i.e. copper) can be circumvented with the use of a secondary catalyst to generate -OH ligands.

scholarly journals Kinetics of Enzymatic Synthesis of Liquid Wax Ester from Oleic Acid and Oleyl Alcohol

2010 ◽  
Vol 59 (3) ◽  
pp. 127-134 ◽  
Author(s):  
Salina Mat Radzi ◽  
Rosfarizan Mohamad ◽  
Mahiran Basri ◽  
Abu Bakar Salleh ◽  
Arbakariya Ariff ◽  
...  
Keyword(s):  
Oleic Acid ◽  
Enzymatic Synthesis ◽  
Oleyl Alcohol ◽  
Wax Ester ◽  
Kinetics Of

scholarly journals PREPARATION OF [AcMI] HSO4 AND USING AS CATALYST FOR ESTERIFICATION

2011 ◽  
Vol 14 (4) ◽  
pp. 61-73
Author(s):  
Thu Ngoc Ha Le ◽  
Thach Ngoc Le
Keyword(s):  
Ionic Liquid ◽  
Chloroacetic Acid ◽  
Molar Ratio ◽  
Hydrogen Sulfate ◽  
Reaction Conditions ◽  
Brønsted Acidic Ionic Liquid ◽  
Acidic Sites ◽  
Concentrated Sulfuric Acid ◽  
Zwitter Ion ◽  
Optimal Reaction

New Bronsted acidic ionic liquid, 1-carboxymethyl-3-methylimidazolium hydrogen sulfate [AcMI]HSO4, has two acidic sites -COOH and HSO4 -. It has been synthesized by three steps. First, 1-carboxymethyl-3-methylimidazolium chloride [AcMI]Cl was prepared by alkylation of 1- methylimidazole with chloroacetic acid (molar ratio is 1.5:1) under microwave irradiation in 6 min (84 % isolated yield). Then, zwitter ion 1-carboxylatmethyl-3-methylimidazolium was obtained by using Ag2O to remove ion chloride Cl- from [AcMI]Cl. At last, concentrated sulfuric acid (98 %) was added into zwitter ion to give 1-carboxymethyl-3-methylimidazolium hydrogen sulfate (yield 96 %). This ionic liquid used as a recyclabe catalyst for the esterification of isopropanol and chloroacetic acid. The optimal reaction conditions were obtained as follows: isopropanol: chloroacetic acid:[AcMI]HSO4 are 1.3:1:0.2, reaction time for 10 min at 60 oC under microvave irradiation. The yield of isopropyl chloroacetate was 86 %. This ionic liquid was removed from ester easily, recovered and recycled without loss of activity.

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