scholarly journals Review: chemical approaches toward catalytic lignin degradation

2021 ◽  
Author(s):  
Sara Gücyeter ◽  
Richard Erpelding ◽  
Magnus S. Schmidt

AbstractLignin is a potentially high natural source of biological aromatic substances. However, decomposition of the polymer has proven to be quite challenging, as the complex bonds are fairly difficult to break down chemically. This article is intended to provide an overview of various recent methods for the catalytic chemical depolymerization of the biopolymer lignin into chemical products. For this purpose, nickel-, zeolite- and palladium-supported catalysts were examined in detail. In order to achieve this, various experiments of the last years were collected, and the efficiency of the individual catalysts was examined. This included evaluating the reaction conditions under which the catalysts work most efficiently. The influence of co-catalysts and Lewis acidity was also investigated. The results show that it is possible to control the obtained product selectivity very well by the choice of the respective catalysts combined with the proper reaction conditions.

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Ana Bjelić ◽  
Brigita Hočevar ◽  
Miha Grilc ◽  
Uroš Novak ◽  
Blaž Likozar

AbstractConventional biorefinery processes are complex, engineered and energy-intensive, where biomass fractionation, a key functional step for the production of biomass-derived chemical substances, demands industrial organic solvents and harsh, environmentally harmful reaction conditions. There is a timely, clear and unmet economic need for a systematic, robust and affordable conversion method technology to become greener, sustainable and cost-effective. In this perspective, deep eutectic solvents (DESs) have been envisaged as the most advanced novel polar liquids that are entirely made of natural, molecular compounds that are capable of an association via hydrogen bonding interactions. DES has quickly emerged in various application functions thanks to a formulations’ simple preparation. These molecules themselves are biobased, renewable, biodegradable and eco-friendly. The present experimental review is providing the state of the art topical overview of trends regarding the employment of DESs in investigated biorefinery-related techniques. This review covers DESs for lignocellulosic component isolation, applications as (co)catalysts and their functionality range in biocatalysis. Furthermore, a special section of the DESs recyclability is included. For DESs to unlock numerous new (reactive) possibilities in future biorefineries, the critical estimation of its complexity in the reaction, separation, or fractionation medium should be addressed more in future studies.


2005 ◽  
Vol 494 ◽  
pp. 363-368 ◽  
Author(s):  
D. Lončarević ◽  
Ž. Čupić

Poly(4-vinylpyridine-co-divinylbenzene)-Co2+ was characterized using infrared spectroscopy (IR), thermogravimetric analysis (TG-DTA), N2-physisorption and polarography. Thermal analysis suggests sufficient thermal stability of the polymer support, under reaction conditions. From polarography measurements, the Co2+ content on polymer-supported catalysts is estimated and it was proved that no significant leaching occurred during the activity tests. At the molecular level, FTIR of P4VP-DVB-Co2+ reveals that the pyridine nitrogen lone pair coordinates to the metal center in the polymeric complex. The obtained P4VP-DVB-Co2+ catalysts performed interesting catalytic activity in reaction of the cyclohexane oxidation with air, indicating that increasing Co2+ content lowers the initiation temperature and raises the decomposition of cyclohexylhydroperoxide.


2013 ◽  
Vol 91 (5) ◽  
pp. 338-347 ◽  
Author(s):  
Anthony F. Cozzolino ◽  
Philip J.W. Elder ◽  
Lucia Myongwon Lee ◽  
Ignacio Vargas-Baca

The secondary bonding interactions that link the supramolecular structures assembled by 1,2,5-chalcogenadiazoles were analyzed through explicit orthogonalization of molecular orbitals (NBO), topological analysis of the electron density (AIM), and the electron localization function (ELF). The results of these analyses are consistent with a bonding description that attributes important covalent and electrostatic character to these interactions. Application of these analyses to the individual molecules highlighted the structural features from which each of those contributions originates, namely the polarity and modest strength of the E–N bond. Both of these effects increase along the series S, Se, Te. Perturbations to the heterocycle electronic structure that result in a weaker and more polar E–N bond cause an increase in the Lewis acidity at the chalcogen centre, which in turn leads to stronger secondary bonding interactions with Lewis bases. Additionally, the contribution of dispersion forces is not negligible and is most important in the case of sulfur.


2019 ◽  
Vol 9 (12) ◽  
pp. 3238-3258 ◽  
Author(s):  
Qiang Lin ◽  
Bing Liu ◽  
Feng Jiang ◽  
Xuejin Fang ◽  
Yuebing Xu ◽  
...  

The formation of cobalt carbide (Co2C) and its catalytic behavior were systematically investigated using realistic reaction conditions.


2018 ◽  
Vol 917 ◽  
pp. 145-151 ◽  
Author(s):  
Nur Syazana Jalani ◽  
Sharifah Zati-Hanani ◽  
Yi Peng Teoh ◽  
Rozaini Abdullah

Recently, interest in plant-mediated synthesis of the silver nanoparticles (AgNPs) is growing among researchers and till now the potential of different plants is still further explored to synthesize nanoparticles. Conventionally, AgNPs are synthesized using chemical and physical methods. However, these methods involve use of toxic and hazardous chemicals which are harmful to health and environment. Therefore, plant-mediated synthesis has been used as environmental friendly alternative to overcome the limitation of conventional methods. The bioactive compounds in plant acts as natural reducing and stabilizing agents which help to increase the rate of synthesis and stabilization of synthesized nanoparticles. Besides, the nanoparticles synthesized using plants are reported to be more stable and the rate of synthesis is much faster compared to other methods. This review focuses on the biosynthesis of AgNPs using plant as natural source plant and the effect of reaction conditions are summarised and discussed.


2012 ◽  
Vol 443-444 ◽  
pp. 1084-1090
Author(s):  
Zhan Ying Guo ◽  
Rong Ran ◽  
Xin Qian Shu ◽  
Ying Ying Yuan ◽  
Yue Zhang ◽  
...  

In order to study the catalytic activity in the preparation of fuel gases from catalytic pyrolysis of coal, the author selects NixOy/γ-Al2O3、CrxOy/γ-Al2O3,AgxOy/γ-Al2O3 and CoxOy/γ-Al2O3, respectively as the metal oxide supported catalysts from the previous experiment’s results. These catalysts have been added to Shenhua coal for a series of experiments. After these experiments, GC (gas chromatography) has been used for the analysis on the yield changes of CO and CH4 which result from the experiments. The results show that all of these catalysts have a positive influence on the yield of CO and CH4. As to the yield of CO, catalytic activity of CrxOy/γ-Al2O3 represents the most prominent performance at medium temperature period and CoxOy/γ-Al2O3 represents the same performance at high temperature period, while NixOy/γ-Al2O3, in which a great number of aluminum acid nickel spinels are reduced into metallic Ni at high temperature period, which results in different catalytic activity center from raw metallic Ni reduced from NiO. Consequently, the former reduced Ni shows outstanding catalytic activity. As to the yield of CH4, four catalysts mentioned above represent either the similar catalytic activity with CO or the individual characteristic —on one hand ,due to the strong adsorption of AgO and CrO3, CH4 gas is changed into H2 via pyrolysis at medium temperature as the yield of CH4 slumps ,on the other hand, due to an enormous amount of H2 production ,there is a drastically chemical reaction between H2 and these catalysts at high temperature, in which the yield of CH4 upswings toward the maximum amount greatly at the same time. Therefore, CrxOy/γ-Al2O3, AgxOy/γ-Al2O3 and CoxOy/γ-Al2O3 are more efficient at medium temperature and high temperature respectively. However, NixOy/γ-Al2O3 demonstrates the positive influence only from 800°Con. All of these results depend on the essence of catalysts to some extent. The study would have some theoretical guidance about increasing the utilization of coal and about industrial application of fuel gases generated from catalytic pyrolysis of coal.


2012 ◽  
Vol 11 (2) ◽  
pp. 1-16
Author(s):  
Sreejarani K Pillai ◽  
O Gheevarghese ◽  
I V Tleane

The present study has undertaken the Friedel-Crafts benzylation of aromatics over the V2O5/ZrO2 catalysts systems. Catalysts with different V2O5 content (0-15wt %) was prepared by wet impregnation method and characterized by XRD, BET surface area, FTIR and 5’V NMR techniques. The surface acidic properties were determined by temperature programmed desorption of NH3, cumene cracking and perylene adsorption. Under the optimized reaction conditions, these catalysts are found to be very effective and considerably more selective than the conventional homogeneous Lewis acid catalysts. The investigation of vanadia systems-catalyzed benzylation of o-xylene with benzyl chloride revealed that the catalytic activity and product selectivity are sensitive to the precise reaction parameters and can be related to the Lewis acidity of the systems. The reaction is found to be very clean and produces the desired monoalkylated product with high yield.


1968 ◽  
Vol 46 (3) ◽  
pp. 451-457 ◽  
Author(s):  
Stanley P. Rowland ◽  
Austin L. Bullock ◽  
Vidabelle O. Cirino ◽  
Clinton P. Wade

The distribution of methylsulfonylethyl substituents at the 2-O-, 3-O-, and 6-O-positions of the monosubstituted D-glucopyranosyl unit of cotton cellulose was found to be a function of the specific reagent and the reaction conditions. The distribution is dependent upon the extent to which rate or equilibrium of reaction at the individual hydroxyl groups is the controlling factor. Under conditions which approach equilibrium in the reaction of methyl vinyl sulfone with cotton cellulose, the ratio of 2-O- to 6-O-substitution is 0.14:1.0. A variety of precursors for methyl vinyl sulfone (i.e., 2-(methylsulfonyl)-ethanol, [2-(rnethylsulfonyl)ethyl]pyridinium chloride, 2-bromoethyl methyl sulfone, and to-[2-(methylsulfonyl)ethyl]ether) react with cotton cellulose under non-equilibrium conditions to generate ratios of 2-O- to 6-O-substitutions as high as 0.44:1.0. The effect of diffusion of reagents into the cotton fiber upon the distribution of substituents is clearly evident in these reactions. Specific modifications of the process of reaction of methyl vinyl sulfone or 2-(methylsulfonyl)ethanol with cotton cellulose yield ratios of substituents in the 2-O- to 6-O-positions as high as 0.8:1.0; this ratio is similar to those which characterize certain rate-controlled Williamson etherification reactions with cotton cellulose.


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