Transformation of HCl during pyrolysis of biomass and its model compounds

Fuel ◽  
2022 ◽  
Vol 309 ◽  
pp. 122139
Author(s):  
Bo Wang ◽  
Xiangpeng Gao ◽  
Jingchun Huang ◽  
Alireza Z. Mofrad ◽  
Zhenqi Wang ◽  
...  
Keyword(s):  
Model Compounds ◽  
Pyrolysis Of Biomass

Pyrolytic Behavior and Kinetic Analysis of Wheat Straw and Lignocellulosic Biomass Model Compound

2013 ◽  
Vol 860-863 ◽  
pp. 550-554 ◽  
Author(s):  
Zhi Qiang Wu ◽  
Shu Zhong Wang ◽  
Jun Zhao ◽  
Lin Chen ◽  
Hai Yu Meng
Keyword(s):  
Activation Energy ◽  
Kinetic Analysis ◽  
Wheat Straw ◽  
Lignocellulosic Biomass ◽  
Nitrogen Atmosphere ◽  
Thermochemical Conversion ◽  
Heating Rates ◽  
Decomposition Rates ◽  
Model Compounds ◽  
Pyrolysis Of Biomass

From a carbon cycle perspective, the thermochemical conversion of lignocellulosic biomass is inherently carbon neutral. Pyrolysis of biomass for energy supplying, such as bio-oil and bio-char, has been attracted much attention worldwide. Successful understanding the fundamental issues about the pyrolysis, including pyrolytic behavior and kinetic analysis of lignocellulosic biomass model compounds and real biomass, is essential for the further understanding and optimizing the pyrolysis process. In this paper, pyrolytic behavior of a typical lignocellulosic agricultural residue (wheat straw) and model compounds (cellulose) were measured through thermogravimetric analysis with various heating rates (10, 20, 40 °C·min-1) under nitrogen atmosphere. The results indicated that the interval of the weight loss for both wheat straw and cellulose moved upwards with the increment of heating rates. The maximum decomposition rates of cellulose were higher than those of wheat straw, and the temperature of maximum decomposition rates increased with the heating rates. Values of activation energy were solved through iso-conversional method. And the average values of activation energy for wheat straw and cellulose were 146.89 kJ·mol-1 and 134.56 kJ·mol-1 calculated from Flynn-Wall-Ozawa method, 144.05 kJ·mol-1 and 130.91 kJ·mol-1 calculated from Kissinger-Akahira-Sunose method, respectively.

Structure Revision of Protoaculeine B, a Posttranslationally Modified N-Terminal Residue in the Peptide Toxin Aculeine B

2020 ◽  
Author(s):  
Raku Irie ◽  
Kei Miyako ◽  
Satoko Matsunaga ◽  
Ryuichi Sakai ◽  
Masato Oikawa
Keyword(s):  
Mass Spectra ◽  
Chemical Reactivity ◽  
Model Compounds ◽  
Structural Revision ◽  
Structure Revision ◽  
Peptide Toxin ◽  
One Step ◽  
Marine Peptide ◽  
Synthetic Models ◽  
Long Chain

<div>Here, we newly propose the structure of protoaculeine B, an N-terminal moiety of the marine peptide toxin aculeine B, as possessing the cis-disubstituted tetrahydro-beta-carboline framework. We prepared two truncated model compounds that lack long-chain polyamine by one-step Pictet-Spengler reaction of tryptophan, and compared the NMR and mass spectra and chemical reactivity with those of natural protoaculeine B. The synthetic models reproduced the profiles of the natural product well, which was conclusive for the structural revision.</div>

RANCANG BANGUN PERANGKAT EKSPERIMENTASI PROSES PIROLISIS BIOMASA GELOMBANG MIKRO

2013 ◽  
Vol 14 (2) ◽  
Author(s):  
Noor Fachrizal
Keyword(s):  
Large Scale ◽  
Continuous Model ◽  
Biomass Energy ◽  
Scale Model ◽  
Small Scale ◽  
Laboratory Apparatus ◽  
Liquid Form ◽  
Large Scale Model ◽  
Bio Oil ◽  
Pyrolysis Of Biomass

Biomass such as agriculture waste and urban waste are enormous potency as energy resources instead of enviromental problem. organic waste can be converted into energy in the form of liquid fuel, solid, and syngas by using of pyrolysis technique. Pyrolysis process can yield higher liquid form when the process can be drifted into fast and flash response. It can be solved by using microwave heating method. This research is started from developing an experimentation laboratory apparatus of microwave-assisted pyrolysis of biomass energy conversion system, and conducting preliminary experiments for gaining the proof that this method can be established for driving the process properly and safely. Modifying commercial oven into laboratory apparatus has been done, it works safely, and initial experiments have been carried out, process yields bio-oil and charcoal shortly, several parameters are achieved. Some further experiments are still needed for more detail parameters. Theresults may be used to design small-scale continuous model of productionsystem, which then can be developed into large-scale model that applicable for comercial use.

Lignin to Value-Added Chemical Synthesis

2020 ◽  
Vol 16 ◽  
Author(s):  
Mahdieh Sharifi ◽  
Ramyakrishna Pothu ◽  
Rajender Boddula ◽  
Inamuddin
Keyword(s):  
Ionic Liquids ◽  
Lignocellulosic Biomass ◽  
Academic Research ◽  
Power Saving ◽  
Value Added ◽  
Glycerol Ether ◽  
Model Compounds ◽  
Lignin Model Compounds ◽  
Biomass Activity ◽  
Lignin Model

Background: There is a developing demand for innovation in petroleum systems replacements. Towards this aim, lignocellulosic biomass suggested as a possible sustainable source for the manufacturing of fuels and produced chemicals. The aims of this paper are to investigate different kinds of β-O-4 lignin model compounds for the production of value-added chemicals in presence of ionic liquids. Especially, a cheap β-O-4 lignin model Guaiacol glycerol ether (GGE) (Guaifenesin) is introduced to produce valuable chemicals and novel products. Methods: Research related to chemical depolymerization of lignocellulosic biomass activity is reviewed, the notes from different methods such as thermal and microwave collected during at least 10 years. So, this collection provides a good source for academic research and it gives an efficient strategy for the manufacturing of novel value-added chemicals at an industrial scale. Results: This research presented that ionic liquid microwave-assisted is a power saving, cost efficient, fast reaction, and clean way with high selectively and purity for production of high value chemicals rather that conversional heating. Guaiacol and catechol are some of these valuable chemicals that is produced from β-O-4 lignin model compounds with high word demands that are capable to produce in industry scale. Conclusion: The β-O-4 lignin model compounds such as Guaiacol glycerol ether (GGE) (Guaifenesin) are good platform for developing food materials, perfumery, biorefinery, and pharmaceutical industry by ionic liquids-assisted lignin depolymerization method.

Study on the precision of the activated charcoal solvent desorption procedure - Correlation of desorption efficiencies

1981 ◽  
Vol 46 (6) ◽  
pp. 1332-1347 ◽  
Author(s):  
Martin Koval
Keyword(s):  
Activated Charcoal ◽  
Carbon Disulphide ◽  
Internal Standard ◽  
Standard Addition ◽  
Published Data ◽  
Single Factor ◽  
Gas Chromatograph ◽  
Model Compounds ◽  
Single Factor Analysis ◽  
Acceptable Agreement

The described method uses activated charcoal sampling tubes for air sampling. Adsorbed compounds are eluted by the static desorption procedure with 1 ml of carbon disulphide, 0.5 ml of the supernatant is filtered off and, after internal standard addition, analysed on a gas chromatograph. Using synthetic calibration mixtures of model organic compounds with air, cumulative sampling and desorption efficiencies for 24 substances were determined for concentration ranges and sample volumes according to current Czechoslovak hygienic standards. Experimental results were treated with the single factor analysis of variance and the precision of the described procedure was estimated for the studied model compounds on the basis of residual sums of squares. Calculated values of cumulative sampling and desorption efficiencies and their precisions were compared with available published data and an acceptable agreement was found. In addition to that, cumulative sampling and desorption efficiencies were also found to be significantly correlated to molar volumes and other related molecular properties for some types of compounds.

Configuration on the C=N double bond of monosubstituted amidines and amidoximes

1989 ◽  
Vol 54 (12) ◽  
pp. 3245-3252 ◽  
Author(s):  
Bernard Tinant ◽  
Janine Dupont-Fenfau ◽  
Jean-Paul Declercq ◽  
Jaroslav Podlaha ◽  
Otto Exner
Keyword(s):  
Double Bond ◽  
Nitrogen Atom ◽  
Steric Effects ◽  
Model Compounds ◽  
X Ray ◽  
Analogous Model

Configuration on the C=N double bond of amidines and amidoximes is controlled by steric effects on the second nitrogen atom but there is a difference in the case of N’-monosubstituted derivatives: amidines prefer E configuration (conformation around the C-N bond sp) and amidoximes Z configuration (conformation ap). This was confirmed by the X-ray structures of two analogous model compounds N,N’-dimethyl-4-nitrobenzamidine (monoclinic, P21c, a = 10.855(3), b = 11.043(3), c = 8.593(3) Å, β = 105.69(2)°, V = 991.8(5) Å3, Z = 4, Dx = 1.29 g cm-3, CuKα, λ = 1.5418 Å, μ = 7.91 cm-1, F(000) = 408, T = 291 K, R = 0.065 for 1 265 observed reflections) and N’-methyl-4-nitrobenzamidoxime (monoclinic, P21/a, a = 6.699(2), b = 24.178(9), c = 6.075(2) Å, β = 106.20(3)°, V = 944.9(6) Å3, Z = 4, Dx = 1.37 g cm-3, CuKα, λ = 1.5418 Å, μ =9.22 cm-1, F(000) = 408, T = 291 K, R = 0.079 for 1 278 observed reflections).

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