Characteristics of Solid Super Acid SO42-/TiO2-Al2O3-SnO2 during Conversion of Glucose to Levulinic Acid

2012 ◽  
Vol 550-553 ◽  
pp. 103-106
Author(s):  
Ying Liu ◽  
Lu Lin ◽  
Xiao Yu Sui ◽  
Jun Ping Zhuang ◽  
Chun Sheng Pang
Keyword(s):  
Binding Energy ◽  
Levulinic Acid ◽  
Diffraction Peak ◽  
Catalyst Amount ◽  
Hydroxymethyl Furfural ◽  
Good Catalytic Activity ◽  
Super Acid ◽  
Diffraction Peaks ◽  
Acid Catalyzed ◽  
Hydrolysis Of

The effects of catalyst amount on the yields of levulinic and hydroxymethyl furfural were investigated during conversion of glucose to levulinic acid catalyzed by solid super acid SO42- / TiO2-Al2O3-SnO2. XRD and XPS were used to analyse the characteristics of solid super acid SO42- / TiO2-Al2O3-SnO2 before reaction and after reaction. The results showed that: solid super acid SO42- / TiO2-Al2O3-SnO2exhibited good catalytic activity in the reaction of hydrolysis of glucose to produce levulinic acid. There were three obvious peaks in these XRD spectra. The peaks on 44.6° and 67.1° were the characteristic diffraction peaks of γ-Al2O3. The anatase characteristic diffraction peak was on 37.4°. The catalyst was steady in the process. The binding energy of S 2p was similar to the binding energy of standard S6+ 2p in the S 2p XPS spectrum of solid super acid. O 1s XPS was double-peaked spectrum. The increase of element C was the main reason of inactivation of catalyst.

Conversion of Glucose to Levulinic Acid Catalyzed by ZSM-5 Loading SO42-/ ZrO2

2013 ◽  
Vol 291-294 ◽  
pp. 249-252
Author(s):  
Ying Liu ◽  
Lu Lin ◽  
Xiao Yu Sui ◽  
Jun Ping Zhuang ◽  
Chun Sheng Pang
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Levulinic Acid ◽  
Temperature Reaction ◽  
Catalyst Amount ◽  
Hydroxymethyl Furfural ◽  
Ft Ir ◽  
Acid Catalyzed ◽  
Molar Percent ◽  
Hydrolysis Of

Hydrolysis of glucose to produce levulinic acid catalyzed by ZSM-5 loading SO42-/ ZrO2 was studied in this paper. The effects of different factors such as catalyst amount, reaction temperature, reaction time on the yields of levulinic acid and hydroxymethyl furfural were investigated. It was found that the highest yield of levulinic acid was 55.03% (molar percent) under the conditions of catalyst amount 3 g, reaction temperature 180 °C and reaction time 2.5 h. Surface structure of catalyst was analyzed by FT-IR, indicating that crystallinity of catalyst was 0.66.

Characterization of ZSM-5 during Conversion of Glucose to Levulinic Acid

2012 ◽  
Vol 260-261 ◽  
pp. 1206-1209
Author(s):  
Ying Liu ◽  
Lu Lin ◽  
Xiao Yu Sui ◽  
Jun Ping Zhuang ◽  
Chun Sheng Pang
Keyword(s):  
Catalytic Activity ◽  
Levulinic Acid ◽  
Characteristic Peak ◽  
Relative Crystallinity ◽  
Al Content ◽  
Hydroxymethyl Furfural ◽  
Good Catalytic Activity ◽  
Acid Catalyzed ◽  
Hydrolysis Of

The effects of catalyst amount on the yields of levulinic and hydroxymethyl furfural were investigated during conversion of glucose to levulinic acid catalyzed by ZSM-5. XRD and XPS were used to analyse the characteristics of ZSM-5 before reaction and after reaction. The results showed that: ZSM-5 exhibited good catalytic activity in the reaction of hydrolysis of glucose to produce levulinic acid. The characteristic peak of ZSM-5 molecular sieve did not change after reaction compared to that of before reaction. The relative crystallinity of ZSM-5 decreased after reaction, which caused the catalytic activity decline. The surface O, Si and Al content of ZSM-5 decreased greatly. The increase of element C was the main reason of inactivation of catalyst.

scholarly journals The effect of pretreatment on methanesulfonic acid-catalyzed hydrolysis of bagasse to levulinic acid, formic acid, and furfural

RSC Advances ◽  
2016 ◽  
Vol 6 (78) ◽  
pp. 74525-74535 ◽  
Author(s):  
Darryn W. Rackemann ◽  
John P. Bartley ◽  
Mark D. Harrison ◽  
William O. S. Doherty
Keyword(s):  
Formic Acid ◽  
Levulinic Acid ◽  
Methanesulfonic Acid ◽  
Acid Catalyzed ◽  
Hydrolysis Of

scholarly journals Acid-Catalyzed Conversion of Cellulose Into Levulinic Acid With Biphasic Solvent System

2021 ◽  
Vol 12 ◽  
Author(s):  
Changyue Ma ◽  
Bo Cai ◽  
Le Zhang ◽  
Junfeng Feng ◽  
Hui Pan
Keyword(s):  
Levulinic Acid ◽  
Value Added ◽  
Acid Catalyst ◽  
Solvent System ◽  
High Yield ◽  
Catalyst Loading ◽  
Amberlyst 15 ◽  
Hydrolysis Of Cellulose ◽  
Acid Catalyzed ◽  
Hydrolysis Of

In this work, acid-catalyzed conversion of cellulose into levulinic acid in a biphasic solvent system was developed. Compared to a series of catalysts investigated in this study, the Amberlyst-15 as a more efficient acid catalyst was used in the hydrolysis of cellulose and further dehydration of derived intermediates into levulinic acid. Besides, the mechanism of biphasic solvent system in the conversion of cellulose was studied in detail, and the results showed biphasic solvent system can promote the conversion of cellulose and suppress the polymerization of the by-products (such as lactic acid).The reaction conditions, such as temperature, time, and catalyst loading were changed to investigate the effect on the yield of levulinic acid. The results indicated that an appealing LA yield of 59.24% was achieved at 200°C and 180 min with a 2:1 ratio of Amberlyst-15 catalyst and cellulose in GVL/H2O under N2 pressure. The influence of different amounts of NaCl addition to this reaction was also investigated. This study provides an economical and environmental-friendly method for the acid-catalyzed conversion of cellulose and high yield of the value-added chemical.

scholarly journals Kinetic Study on the Acid-Catalyzed Hydrolysis of Cellulose to Levulinic Acid

2007 ◽  
Vol 46 (6) ◽  
pp. 1696-1708 ◽  
Author(s):  
B. Girisuta ◽  
L. P. B. M. Janssen ◽  
H. J. Heeres
Keyword(s):  
Kinetic Study ◽  
Levulinic Acid ◽  
Hydrolysis Of Cellulose ◽  
Acid Catalyzed ◽  
Hydrolysis Of

The effect of polymeric and model imidazolium halides on the rate of hydrolysis of 4-acetoxy-3-nitrobenzoic acid

1985 ◽  
Vol 50 (4) ◽  
pp. 845-853 ◽  
Author(s):  
Miloslav Šorm ◽  
Miloslav Procházka ◽  
Jaroslav Kálal
Keyword(s):  
Catalyst Concentration ◽  
Low Molecular Weight ◽  
Imidazolium Chloride ◽  
First Order ◽  
Nitrobenzoic Acid ◽  
Rate Of Hydrolysis ◽  
Acid Catalyzed ◽  
Hydrolysis Of ◽  
Ethanol In Water ◽  
Direct Attack

The course of hydrolysis of an ester, 4-acetoxy-3-nitrobenzoic acid catalyzed with poly(1-methyl-3-allylimidazolium bromide) (IIa), poly[l-methyl-3-(2-propinyl)imidazolium chloride] (IIb) and poly[l-methyl-3-(2-methacryloyloxyethyl)imidazolium bromide] (IIc) in a 28.5% aqueous ethanol was investigated as a function of pH and compared with low-molecular weight models, viz., l-methyl-3-alkylimidazolium bromides (the alkyl group being methyl, propyl, and hexyl, resp). Polymers IIb, IIc possessed a higher activity at pH above 9, while the models were more active at a lower pH with a maximum at pH 7.67. The catalytic activity at the higher pH is attributed to an attack by the OH- group, while at the lower pH it is assigned to a direct attack of water on the substrate. The rate of hydrolysis of 4-acetoxy-3-nitrobenzoic acid is proportional to the catalyst concentration [IIc] and proceeds as a first-order reaction. The hydrolysis depends on the composition of the solvent and was highest at 28.5% (vol.) of ethanol in water. The hydrolysis of a neutral ester, 4-nitrophenyl acetate, was not accelerated by IIc.

Benzyl ethers of methyl α-D-glucopyranoside

1980 ◽  
Vol 45 (7) ◽  
pp. 1959-1963 ◽  
Author(s):  
Dušan Joniak ◽  
Božena Košíková ◽  
Ludmila Kosáková
Keyword(s):  
Kinetic Study ◽  
Spectrophotometric Determination ◽  
Reductive Cleavage ◽  
Ether Bond ◽  
Benzyl Ethers ◽  
Acid Catalyzed ◽  
Model Substances ◽  
Hydrolysis Of

Methyl 4-O-(3-methoxy-4-hydroxybenzyl) and methyl 4-O-(3,5-dimethoxy-4-hydroxybenzyl)-α-D-glucopyranoside and their 6-O-isomers were prepared as model substances for the ether lignin-saccharide bond by reductive cleavage of corresponding 4,6-O-benzylidene derivatives. Kinetic study of acid-catalyzed hydrolysis of the compounds prepared was carried out by spectrophotometric determination of the benzyl alcoholic groups set free, after their reaction with quinonemonochloroimide, and it showed the low stability of the p-hydroxybenzyl ether bond.

Cyclization and acid-catalyzed hydrolysis of O-benzoylbenzamidoximes

1986 ◽  
Vol 51 (12) ◽  
pp. 2786-2797
Author(s):  
František Grambal ◽  
Jan Lasovský
Keyword(s):  
Reaction Rate ◽  
Kinetic Isotope ◽  
Acid Base Equilibrium ◽  
Mineral Acids ◽  
Kinetics Of Formation ◽  
Acid Catalyzed ◽  
Ph Scale ◽  
Kinetics Of ◽  
Hydrolysis Of ◽  
Derivatives Of

Kinetics of formation of 1,2,4-oxadiazoles from 24 substitution derivatives of O-benzoylbenzamidoxime have been studied in sulphuric acid and aqueous ethanol media. It has been found that this medium requires introduction of the Hammett H0 function instead of the pH scale beginning as low as from 0.1% solutions of mineral acids. Effects of the acid concentration, ionic strength, and temperature on the reaction rate and on the kinetic isotope effect have been followed. From these dependences and from polar effects of substituents it was concluded that along with the cyclization to 1,2,4-oxadiazoles there proceeds hydrolysis to benzamidoxime and benzoic acid. The reaction is thermodynamically controlled by the acid-base equilibrium of the O-benzylated benzamidoximes.

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