A study of the properties of a composite asphalt binder using liquid products of wood fast pyrolysis

2016 ◽  
Vol 9 (2) ◽  
pp. 181-184 ◽  
Author(s):  
G. M. Fayzrakhmanova ◽  
S. A. Zabelkin ◽  
A. N. Grachev ◽  
V. N. Bashkirov
Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 494
Author(s):  
Xueli Hou ◽  
Zhen Li ◽  
Zhijun Zhang

Boric acid is recently proved to be a good substitute for conventional acidic catalytic materials. However, few studies used boric acid as a catalyst in biomass pyrolysis. This study focused on the catalytic effects of boric acid (BA) on pyrolysis behaviors of woody biomass. The birch wood flour (WF) was used as feedstock and treated by impregnation of boric acid solution. Both untreated and boric acid-treated samples (BW) were characterized by FTIR and SEM. Thermogravimetry (TG) and pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC/MS) techniques were used for studying mass loss, composition, and distribution of evolved volatiles formed from pyrolysis process. Additionally, a small fixed-bed pyrolyzer with an amplificated loading amount was used to prepare liquid products, and further, GC/MS were used to analyze the composition of these liquid products. Different pyrolysis temperatures and boric acid/wood flour mass ratios were also studied. The main results are as follows. Boric acid infiltrated into both cell cavity and cell wall through impregnation treatment. FTIR analysis showed that boric acid reacted with wood flour to form B-O-C bond during the treatment. After the treatment of boric acid, the initial degradation temperatures and residual carbon contents were increased, while the maximum weight loss rates were decreased. Boric acid significantly altered the composition and distribution of volatile pyrolysis products of wood flour. It significantly increased the contents of small molecule compounds such as acetic acid and furfural but, decreased the contents of phenol derivatives with high molecular weights. And these changes became more pronounced as the temperature increased. When mass ratio of boric acid (BA) to wood flour (WF) was 2, the acetic acid accounted for 91.28% of the total product in the pyrolysis liquid, which was 14 times higher than that of untreated wood flour. Boric acid effectively catalyzed fast pyrolysis of woody biomass to selectively produce acetic acid


2018 ◽  
Vol 11 (2) ◽  
pp. 131-134
Author(s):  
S. A. Zabelkin ◽  
A. N. Grachev ◽  
G. M. Bikbulatova ◽  
A. E. Yakovleva ◽  
A. A. Makarov ◽  
...  

2017 ◽  
Vol 4 (1) ◽  
pp. 13-18
Author(s):  
Joko Sulistyo ◽  
Toshimitsu Hata ◽  
Sensho Honma ◽  
Ryohei Asakura ◽  
Sri Nugroho Marsoem

The study on catalytic pyrolysis decomposition of Shorea leprosula wood biomass to form aromatic compounds in fast pyrolysis was performed by pyrolytic-gas chromatography/mass spectroscopy (Py-GC/MS) and transmission electron microscope (TEM) - electron energy-loss spectroscopy (EELS) to analyze the chemical compound and solid residue microstructure. Py-GC/MS and TEM-EELS analysis showed that the fast pyrolysis increased the decomposition of hardwood, in which in the presence of ZSM-5 catalyst, the liquid products from wood decomposition was then diffused into the pore of ZSM-5 catalyst to form aromatics including benzene, toluene, styrene, naphthalenes and indanes. The carbonaceous solid compounds or cokes were not deposited on the surface of pores of ZSM-5 catalyst in the fast pyrolysis, as shown by the EELS spectrum that exhibited no detection of any solid carbonaceous compound in the solid residue.


2018 ◽  
Vol 20 (5) ◽  
pp. 1182-1200 ◽  
Author(s):  
Sergey Zabelkin ◽  
Guzeliia Bikbulatova ◽  
Andrey Grachev ◽  
Vladimir Bashkirov ◽  
Sergey Burenkov ◽  
...  

Author(s):  
Jan Piskorz ◽  
Desmond St. A. G. Radlein ◽  
Donald S. Scott ◽  
Stefan Czernik

2019 ◽  
Vol 5 (12) ◽  
pp. 37-46
Author(s):  
K. Chalov ◽  
Yu. Lugovoy ◽  
Yu. Kosivtsov ◽  
E. Sulman

This paper presents a study of the process of thermal degradation of crosslinked polyethylene. The kinetics of polymer decomposition was studied by thermogravimetry. Crosslinked polyethylene showed high heat resistance to temperatures of 400 °C. The temperature range of 430–500 °C was determined for the loss of the bulk of the sample. According to thermogravimetric data, the decomposition process proceeds in a single stage and includes a large number of fracture, cyclization, dehydrogenation, and other reactions. The process of pyrolysis of a crosslinked polymer in a stationary-bed metal reactor was investigated. The influence of the process temperature on the yield of solid, liquid, and gaseous pyrolysis products was investigated. The optimum process temperature was 500 °C. At this temperature, the yield of liquid and gaseous products was 85.0 and 12.5% (mass.), Respectively. Samples of crosslinked polyester decomposed almost completely. The amount of carbon–containing residue was 3.5% by weight of the feedstock. With increasing temperature, the yield of liquid products decreased slightly and the yield of gaseous products increased, but their total yield did not increase. For gaseous products, a qualitative and quantitative composition was determined. The main components of the pyrolysis gas were hydrocarbons C1–C4. The calorific value of pyrolysis gas obtained at a temperature of 500 °C was 17 MJ/m3. Thus, the pyrolysis process can be used to process crosslinked polyethylene wastes to produce liquid hydrocarbons and combustible gases.


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