Exploration of Chemical Oxidation of p-Cymene

2011 ◽  
Vol 396-398 ◽  
pp. 1132-1137
Author(s):  
Liang Wu Bi ◽  
Qiu Ge Zhang ◽  
Zhen Dong Zhao ◽  
Da Wei Li
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Benzoic Acid ◽  
Sulphuric Acid ◽  
Potassium Permanganate ◽  
Reaction Temperature ◽  
Chemical Oxidation ◽  
Molar Ratio ◽  
Acid Reaction ◽  
By Products

The chemical oxidation of p-cymene was preliminarily studied by several oxidants. The conversion of p-cymene and selectivity of p-cymen-8-ol were both influenced by the factors such as dosage of oxidant, dosage of sulphuric acid, reaction time, reaction temperature and solvent variety. The reasonable oxidation conditions were molar ratio of p-cymene to potassium permanganate 1:3, molar ratio of sulphuric acid to potassium permanganate 0.13:1, mixture of water and acetic acid (1:1, v/v) as solvent, reaction temperature 80 °C and reaction time 9 h. The conversion of p-cymene and selectivity of p-cymen-8-ol were respectively 92.21 % and 69.65 % in the reasonable oxidation conditions. The by-products of p-cymene oxidation mainly included p-iso-propyl benzoic acid, p-isopropyl benzaldehyde and p-methyl acetophenone.

Catalytic Synthesis of Ethyl Acetate Using Ti2SnC

2013 ◽  
Vol 634-638 ◽  
pp. 628-631
Author(s):  
Yun Hui Long ◽  
Jun Ming Guo ◽  
Du Shu Huang ◽  
Gui Yang Liu
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Ethyl Acetate ◽  
Reaction Temperature ◽  
Conversion Rate ◽  
Reaction System ◽  
Catalytic Performance ◽  
Catalytic Synthesis ◽  
Molar Ratio ◽  
The Ideal

The catalytic synthesis of ethyl acetate from ethanol and acetic acid using Ti2SnC in liquid phase under the atmospheric pressure was studied. The influences of some factors such as catalyst usage, initial reactant molar ratio, reaction temperature and reaction time on acetic acid conversion rate of this reaction system were investigated. The acetic acid conversion rate of 88.12% is achieved while the molar ratio of alcohol and acid is 1:3.6, the amount of catalyst is 0.2000 g, the reaction temperature is 80 °C and the reaction time is 30min. The catalyst Ti2SnC is the ideal catalyst for synthesis of ethyl acetate for good catalytic performance, non-corrosive to equipment, easily separated from product and used repeatedly.

Esterification of glycerol with acetic acid using a sulfonated polyphenylene sulfide non-woven fabric as a catalyst

2020 ◽  
Vol 18 (12) ◽  
Author(s):  
Xueyang Li ◽  
Jiao Zhang ◽  
Yunfei Song ◽  
Yanhong Ji ◽  
Mohammad Younas ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Polyphenylene Sulfide ◽  
Woven Fabric ◽  
Molar Ratio ◽  
Solid Catalyst ◽  
Glycerol Conversion ◽  
Good Catalytic Activity ◽  
Reaction Cycles

AbstractIn this work, the esterification of glycerol with acetic acid (HOAc) was investigated under sulfonated polyphenylene sulfide non-woven fabric (SPSF) as a solid catalyst. The effects of the amount of catalyst, reaction temperature, molar ratio of glycerol to HOAc and the reaction time on the esterification were studied in detail. It was found that SPSF has good catalytic activity and stability. Under the reaction conditions of the molar ratio of glycerol/HOAc of 1:6 (glycerol 0.1 mol), the reaction temperature of 110 °C, the amount of catalyst of 3 g, and the reaction time of 2 h, the glycerol conversion and the selectivity to diacetin (DAG) reached upto 96 and 56.1%, respectively. Reusability test of SPSF showed that no significant declination in the glycerol conversion and the selectivity was observed after five reaction cycles. The experimental results proved the esterification of glycerol with HOAc by SPSF a promising and green process.

Synthesis of Fragrance 1-(3,3-dimethylcyclohexyl)Ethyl Acetate

2013 ◽  
Vol 781-784 ◽  
pp. 983-987
Author(s):  
De Li Shen ◽  
Xin He ◽  
Wei Guan ◽  
Yu Ping Liu ◽  
Bao Guo Sun
Keyword(s):  
Acetic Acid ◽  
Sulfuric Acid ◽  
Reaction Time ◽  
Ethyl Acetate ◽  
Reaction Temperature ◽  
Raw Materials ◽  
Molar Ratio ◽  
Gas Chromatography Mass Spectrometry ◽  
Floral Odor ◽  
Odor Evaluation

1-(3,3-dimethylcyclohexyl) ethyl acetate was synthesized by the reaction of dihydromycene with acetic acid in the presence of sulfuric acid. The effecting factors including the amount of catalyst, the reaction temperature, the molar ratio of raw materials and the reaction time were investigated. The experimental results showed that the molar raio of the dihydromyrcene to acetic acid to sulfuric acid was 1:3:0.2, the reaction temperature is 60 °C and the reaction time was 6.5 h. The yield reached 45.3%. The structure of product was characterized by gas chromatography, mass spectrometry, infrared spectroscopy and nuclear magnetic resonance. The odor evaluation result indicated that the product had a sweet, woody, floral odor.

Study on Preparation of Biodiesel with Monomer Acid

2014 ◽  
Vol 521 ◽  
pp. 72-75
Author(s):  
Xiao Feng Liu
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Catalyst Concentration ◽  
Diesel Oil ◽  
Molar Ratio ◽  
Esterification Reaction ◽  
Optimum Conditions ◽  
Toluenesulfonic Acid ◽  
Acid Reaction ◽  
Single Factor Experiment

An esterification reaction of monomer acid with methanol using p-toluenesulfonic acid as catalyst for the preparation of biodiesel was studied. The process variables that influence the esterification of monomer acid, such as catalyst concentration, molar ratio of methanol to acid, reaction time and reaction temperature, were investigated and optimized. Through the single factor experiment, the optimum conditions obtained for the esterification were molar ratio of methanol to acid 3:1, usage amount of p-toluenesulfonic acid 6% and reaction time 3h, reaction temperature 70°C.The produced biodiesel was found to exhibit fuel properties within the limits prescribed by the latest American Standards for Testing Material (ASTM) and 0#diesel oil.

Catalytic Synthesis of N-Butyl Acetate by Silicotungstic Acid Supported on Bentonite

2012 ◽  
Vol 550-553 ◽  
pp. 362-365
Author(s):  
Jian Zhong Jin
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Butyl Acetate ◽  
Molar Ratio ◽  
Main Reaction ◽  
Incipient Wetness Impregnation ◽  
Impregnation Method ◽  
Silicotungstic Acid ◽  
Acid Loading

A series of solid acid catalysts were synthesized by incipient wetness impregnation method by varying the wt% of silicotungstic acid on bentonite. Silicotungstic acid supported on bentonite was used to catalytic synthesise of n-butyl acetate with acetic acid and n-butyl alcohol . The main reaction parameters such as silicotungstic acid loading on bentonite, the amount of catalyst, molar ratio of reactants, reaction temperature and reaction time have been investigated. The optimum conditions were determined as follows : silicotungstic acid loading on bentonite 20 wt %, catalyst 0.7 g , mole ratio of n-butanol to acetic acid 1:1.1, reaction temperature 98 °C and reaction time 2 h . The esterification yield of n-butyl acetate was about 98.2 %. The catalyst could be used repeatedly for many times without distinct loss in activity.

Study on the Synthesis of Isoamyl Acetate Catalyzed by Strong Acidic Cation Exchange Resin

2011 ◽  
Vol 396-398 ◽  
pp. 2411-2415 ◽  
Author(s):  
Ping Lan ◽  
Li Hong Lan ◽  
Tao Xie ◽  
An Ping Liao
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Cation Exchanger ◽  
Cation Exchange Resin ◽  
Isoamyl Acetate ◽  
Molar Ratio ◽  
Esterification Reaction ◽  
Reaction Conditions ◽  
Optimum Reaction

Isoamyl acetate was synthesized from isoamylol and glacial acetic acid with strong acidic cation exchanger as catalyst. The effects of reaction conditions such as acid-alcohol ratio, reaction time, catalyst dosage to esterification reaction have been investigated and the optimum reaction conditions can be concluded as: the molar ratio of acetic acid to isoamylol 0.8:1, reaction time 2h, 25 % of catalyst (quality of acetic acid as benchmark). The conversion rate can reach up to 75.46%. The catalytic ability didn’t reduce significantly after reusing 10 times and the results showed that the catalyst exhibited preferably catalytic activity and reusability.

scholarly journals Optimization of Enzymatic Synthesis of Betulinic Acid Amide in Organic Solvent by Response Surface Methodology (RSM)

2019 ◽  
Vol 19 (4) ◽  
pp. 849
Author(s):  
Nurul Atikah Amin Yusof ◽  
Nursyamsyila Mat Hadzir ◽  
Siti Efliza Ashari ◽  
Nor Suhaila Mohamad Hanapi ◽  
Rossuriati Dol Hamid
Keyword(s):  
Response Surface Methodology ◽  
Reaction Time ◽  
Response Surface ◽  
Reaction Temperature ◽  
Betulinic Acid ◽  
Enzymatic Synthesis ◽  
Acid Amide ◽  
Molar Ratio ◽  
Percentage Yield ◽  
Substrate Molar Ratio

Optimization of the lipase catalyzed enzymatic synthesis of betulinic acid amide in the presence of immobilized lipase, Novozym 435 from Candida antartica as a biocatalyst was studied. Response surface methodology (RSM) and 5-level-4-factor central-composite rotatable design (CCRD) were employed to evaluate the effects of the synthesis parameters, such as reaction time (20–36 h), reaction temperature (37–45 °C), substrate molar ratio of betulinic acid to butylamine (1:1–1:3), and enzyme amounts (80–120 mg) on the percentage yield of betulinic acid amide by direct amidation reaction. The optimum conditions for synthesis were: reaction time of 28 h 33 min, reaction temperature of 42.92 °C, substrate molar ratio of 1:2.21, and enzyme amount of 97.77 mg. The percentage yield of actual experimental values obtained 65.09% which compared well with the maximum predicted value of 67.23%. The obtained amide was characterized by GC, GCMS and 13C NMR. Betulinic acid amide (BAA) showed a better cytotoxicity compared to betulinic acid as the concentration inhibited 50% of the cell growth (IC50) against MDA-MB-231 cell line (IC50 < 30 µg/mL).

Synthesis of light-colored rosin glycerol ester

Holzforschung ◽  
2007 ◽  
Vol 61 (5) ◽  
pp. 499-503 ◽  
Author(s):  
Shifa Wang
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Softening Point ◽  
Acid Number ◽  
Total Weight ◽  
Molar Ratio ◽  
Optimal Dosage ◽  
Weight Percentage ◽  
Glycerol Ester ◽  
Ring Method

Abstract A light-colored rosin glycerol ester was synthesized from gum rosin and glycerol in the presence of a highly effective decolorizing agent. The effects of the type and dosage of the decolorizing agent and the reaction temperature and time on the yield, softening point, color, and acid number of the rosin glycerol ester were investigated. Experimental results showed that 4,4′-thio-bis(6-tert-butyl-3-methyl phenol) was the best decolorizing agent. It promoted esterification at an optimal dosage of 0.5% (based on the weight percentage of starting material rosin). Suitable conditions for esterification of rosin and glycerol were: reaction temperature, 260–270°C; reaction time, 6–8 h; and rosin/glycerol molar ratio, 2.5:1 (mol mol-1). The characteristics of the rosin glycerol ester obtained under these conditions were as follows: softening point, 90–94°C (ball and ring method); color, 1–2 (Gardner value); acid number, 7–8; and yield, >88% (based on the total weight of rosin and glycerol). The selected additive has a multifunctional effect involving bleaching, disproportionation, and catalysis.

Synthesis and Characterization of a New Phosphorus-Containing Curing Agent PPDTA

2019 ◽  
Vol 953 ◽  
pp. 185-190
Author(s):  
Yong Li Peng ◽  
Ni An Zhuo ◽  
Can Zhang
Keyword(s):  
Infrared Spectroscopy ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Molar Ratio ◽  
Synthesis And Characterization ◽  
Curing Agent ◽  
Phosphorus Containing ◽  
Three Factor

A new phosphorus-containing flame-retardant curing agent PPDTA was synthesized from phenylphosphonic dichloride (PPD) and 3-amino-1,2,4-triazole (TA) in tetrahydrofuran solvent to improve the flame retardancy of epoxy resin. The structure of the compound was analyzed and confirmed by infrared spectroscopy. The effects of reaction time, reaction temperature and ratio of reactants on yield were studied by using three-factor three-level orthogonal experiment. The results show that the yield of PPDTA can reach 86.4%, when the reaction time is 10h, reaction temperature is 70 °Cand the molar ratio of TA to PPD is 2.2:1.

Preparation and Characterization of Cationic Cassia Tora Gum

2013 ◽  
Vol 781-784 ◽  
pp. 526-530 ◽  
Author(s):  
Shao Ying Li ◽  
Chun Mei Niu ◽  
Hua Yu Zhong
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Water Solubility ◽  
Cold Water ◽  
Water Solution ◽  
Molar Ratio ◽  
Reaction Conditions ◽  
Cassia Tora ◽  
Dispersing Agent

Series of cationic cassia tora gum (CCTG) were synthesized using 3-chloro-2-hydroxypropyl trimethyl ammonium chloride (CHPTAC) as cationic etherifying agent, isopropanol-water solution as dispersing agent, in presence of sodium hydroxide under different reaction conditions. The optimum ratio for preparing the cationic cassia tora gum are that CHPTAC-CTG molar ratio is 0.6:1; NaOH-CHPTAC molar ratio is 1.3:1.The optimum conditions are that reaction temperature is 55°Cand reaction time is 3.5 h. The cold water solubility was improved apparently. The solution transmittance has corresponding relationship with the nitrogen content (N%) in the certain range, and the maximum transmittance is up to 87.2%. N% increased with the increase of reaction time and stable N% can be obtained in shorter reaction time at higher reaction temperature. The products were characterized by 13C-NMR. The heat resistance of CTG and CCTG were analyzed.

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