Thermal and geochemical characterization of Lokpanta oil shales,Nigeria

Thermal decomposition of Lokpanta oil shale from Nigeria was studied by non-isothermal thermogravimetry (TG) and differential thermal analysis (DTA). The experiments were performed in an inert environment with a temperature range of 25 to 600 °C. The geochemical characteristics of the oil shale were also investigated by Rock Eval. pyrolysis. Thermal breakdown of the kerogen content of the oil shale takes place mainly at the temperature range of 300 to 570 °C. The estimated decomposable kerogen content of the oil shale ranges from 4.55 to 9.64 wt.%. The activation energies of the pyrolysis process vary from 73.2 to 75.0 kJ/mol. The DTA data reveals the exothermic nature of the decomposition process. The results from the geochemical analysis indicate that the oil shale contains sufficient, good quality kerogen to generate both oil and gas upon pyrolysis.     

Slow and fast pyrolysis of Douglas-fir lignin: Importance of liquid-intermediate formation on the distribution of products

The formation of liquid intermediates and the distribution of products were studied under slow and fast pyrolysis conditions. Results indicate that monomers are formed from lignin oligomeric products during secondary reactions, rather than directly from the native lignin. Lignin from Douglas-fir (Pseudotsuga menziesii) wood was extracted using the milled wood enzyme lignin isolation method. Slow pyrolysis using a microscope with hot-stage captured the liquid formation (>150 °C), shrinking, swelling (foaming), and evaporation behavior of lignin intermediates. The activation energy (E_a) for 5–80% conversions was 213 kJ mol⁻¹, and the pre-exponential factor (log A) was 24.34. Fast pyrolysis tests in a wire mesh reactor were conducted (300–650 °C). The formation of the liquid intermediate was visualized with a fast speed camera (250 Hz), showing the existence of three well defined steps: formation of lignin liquid intermediates, foaming and liquid intermediate swelling, and evaporation and droplet shrinking. GC/MS and UV-Fluorescence of the mesh reactor condensate revealed lignin oligomer formation but no mono-phenols were seen. An increase in pyrolytic lignin yield was observed as temperature increased. The molar mass determined by ESI-MS was not affected by pyrolysis temperature. SEM of the char showed a smooth surface with holes, evidence of a liquid intermediate with foaming; bursting from these foams could be responsible for the removal of lignin oligomers. Py-GC/MS studies showed the highest yield of guaiacol compounds at 450–550 °C.     

Effect of temperature on the fast pyrolysis of organic-acid leached pinewood; the potential of low temperature pyrolysis

In this paper, we have evaluated the potential of organic acid (mixture of acetic, formic and propionic acid) leaching of biomass and subsequent fast pyrolysis to increase the organic oil, sugars and phenols yield by varying the fluidized bed temperature between 360 °C and 580 °C (360 °C, 430 °C, 480 °C, 530 °C, and 580 °C). The pyrolysis of acid leached pinewood resulted in more organic oil and less water and residue compared to untreated pinewood over the whole temperature range. Below 500 °C the difference was most profound; for acid leached pinewood at 360 °C the organic oil was already 650 g kg⁻¹ pine with a sugar yield of 230 g kg⁻¹ pine. At this low pyrolysis temperature no bed agglomeration was observed for acid leached pine whereas at the higher temperatures tested agglomerates were found, which were identified to be clusters of fluidization sand glued together by sticky pyrolysis products (melt). Low reactor temperatures also favored the production of monomeric phenols, though their absolute yields remained low for both untreated and leached pine (maximum: 23 g kg⁻¹ pine, 80 g kg⁻¹ lignin). GPC, GC/MS and UV-fluorescence spectroscopy showed that acid leaching did not influence significantly the yield and molecular size of the aromatic fraction in the produced pyrolysis oils. Back impregnation of the removed AAEMs into leached biomass revealed that the effects of the applied acid leaching, both with respect to the product yields and bed agglomeration, can be mainly assigned to the removal of AAEMs.     

The influence of temperature and heating rate on the slow pyrolysis of biomass

The slow pyrolysis of biomass in the form of pine wood was investigated in a static batch reactor at pyrolysis temperatures from 300 to 720°C and heating rates from 5 to 80 K min⁻¹. The compositions and properties of the derived gases, pyrolytic oils and solid char were determined in relation to pyrolysis temperatures and heating rates. In addition, the wood and the major components of the wood—cellulose, hemicellulose and lignin—were pyrolysed in a thermogravimetric analyser (TGA) under the same experimental conditions as in the static batch reactor. The static batch reactor results showed that as the pyrolysis temperature was increased, the percentage mass of solid char decreased, while gas and oil products increased. There was a small effect of heating rate on product yield. The lower temperature regime of decomposition of wood showed that mainly H₂O, CO₂ and CO were evolved and at the higher temperature regime, the main decomposition products were oil, H₂O, H₂, hydrocarbon gases and lower concentrations of CO and CO₂. Fourier transformation infra-red spectroscopy and elemental analysis of the oils showed they were highly oxygenated. The TGA results for wood showed two main regimes of weight loss, the lower temperature regime could be correlated with the decomposition of hemicellulose and the initial stages of cellulose decomposition whilst the upper temperature regime correlated mainly with the later stages of cellulose decomposition. Lignin thermal decomposition occurred throughout the temperature range of pyrolysis.     

Thermal degradation of corn starch based biodegradable plastic plates and determination of kinetic parameters by isoconversional methods using thermogravimetric analyzer

Oil shortage and awareness of environment pollution leads to the extensive use of biodegradable starch-based materials against synthetic plastics. The accumulated wastes of these plastics takes more time for natural recycling and the process is complex. Therefore the best option of recycling would be to convert these polymers into a source of energy by pyrolysis. So to understand the pyrolytic behaviour, kinetics of such waste plastics is studied by using thermogravimetric analysis at different heating rates of 10 °C, 20 °C, 40 °C, 60 °C, 80 °C and 100 °C in nitrogen atmosphere followed by characterization of the pyrolysis products. The kinetic parameters are obtained for two major stages of decomposition in two different temperature ranges 250–620 °C and 620–855 °C by iso-conversional methods such as Friedman, Coats-Redfern, FWO and Kissinger methods. The regression coefficient data (>0.9) of kinetic plots obtained for different methods best fits to the kinetic equation. Empirical formula of the compound is determined by ultimate analysis is CH_2.214S_0.0018O_0.6910. Proximate analysis gives the idea of volatile component which is74.33%. The range of average value of activation energy is 120.7013 kJ/mol to 140.7707 kJ/mol for the biodegradable plastic plate with different conversion (0.1–0.6) and (0.1–0.3) respectively at two different temperatures. The pyrolysis products obtained using a semi-batch reactor are characterized to know their composition and other properties.     

Investigation on the decomposition of chemical compositions during hydrothermal conversion of dewatered sewage sludge

Hydrothermal conversion (HC) can be used to convert sewage sludge into fuel-like products. The investigation of biomass compositions conversion can facilitate the understanding of reaction pathways. HC of dewatered sewage sludge (DSS) is conducted in sub-/supercritical water with batch reactors. Hemicellulose has the highest conversion efficiency of 99.1 wt %, followed by crude protein, cellulose, lignin, and lipid/oil. The total gas and H₂ yields increase slowly from 200 to 300 °C, then sharply rise up from 350 to 450 °C. At 450 °C, the H₂ yield reaches to the maximum of 0.70 mol/kg organic matter. HC of DSS includes reactants degradation to intermediates and final products formation from intermediates. The water-soluble products (WSPs) are formed throughout the HC process, the oil-phase products (OPs) are mostly produced at low temperatures (250–350 °C), and char and gases are mainly generated at higher temperatures (above 350 °C).     

Experimental study of the pyrolysis of waste bitumen for oil production

This work focuses on bitumen slow pyrolysis. Mass and energy yields of oil, solid and gas were obtained from pyrolysis experiments using a semi-batch reactor in a nitrogen atmosphere, under three non-isothermal conditions (maximum temperature: 450 °C, 500 °C and 550 °C). The effect of temperature on the product yields was discussed. The gas compositions were analysed using gas chromatography (GC) and the heating value of oil and solid residue was also measured. Using a thermo-gravimetric analyser, kinetic parameters were evaluated through Ozawa-Flynn-Wall (OFW) method. Results showed that oil yield is maximum at 500 °C (50%). Moreover, gas yield increased with increasing pyrolysis temperature from 18% to 36%. On the other hand, solid yield showed an opposite trend: it decreased from 39% to 32%. As regard energy yields, they showed a similar trend with the mass ones. H_2, CH₄, C₂H₄, C₂H₆ and C₃H₈ are the main components of the produced gas phase. It has been noticed that the recovery of bitumen to liquid oil through pyrolysis process had a great potential since the oil produced had high calorific value comparable with commercial fuels.     

Influence of temperature and steam on the products from the flash pyrolysis of Jordan oil shale

Oil shale samples from the Sultani deposit in the south of Jordan, were pyrolysed in a semi‐continuous fluidized bed reactor under nitrogen and nitrogen/steam atmosphere. The pyrolysis temperature between 400 and 650°C were investigated. Increasing the pyrolysis temperature from 400 to 520°C caused a large increase in the oil yield. Further increase of the pyrolysis temperature resulted in a decrease in oil yield and a large increase in the evolved gases. This increase in the hydrocarbon gas yield was attributed to oil thermal cracking reactions. The evolved gases were composed of H₂, CO, CO₂, and hydrocarbons from C₁ to C₄. The presence of steam improved the oil yield which may be a result of reducing the degree of decomposition. The derived oils were fractionated into chemical classes using mini‐column liquid chromatography. Copyright © 2002 John Wiley & Sons, Ltd.     

油棕废弃物及生物质三组分的热解动力学研究

主要利用热重分析仪(TG)对油棕废弃物和生物质的三组分(半纤维素,纤维素和木质素)的热解特性进行了系统研究,对比分析了热解特性,计算了其热解动力学参数,并研究了升温速率对生物质热解特性的影响。研究发现半纤维素和纤维素易于热降解而木质素难于热解;油棕废弃物的热解可以化分为:干燥、半纤维素热解、纤维素热解和木质素热解4个阶段;生物质的热解反应主要是一级反应,油棕废弃物的活化能很低,约为60kJ/kg;升温速率对生物质影响很大,随升温速率加快,生物质热解温度升高,热解速率降低。     

Non-isothermal pyrolysis of the mixtures of waste automobile lubricating oil and polystyrene in a stirred batch reactor

Kinetic tests on pyrolysis of the mixture of waste automobile lubricating oil (WALO) and polystyrene (PS) were carried out with a thermogravimetric analysis (TGA) technique at a heating rate of 0.5 °C/min, 1.0 °C/min and 2.0 °C/min in a stirred batch reactor. WALO and PS were mainly decomposed 400–455 °C and 370–410 °C, respectively. The mixture of WALO and PS, however, was decomposed between 355 °C and 470 °C, and decomposition proceeded in two broad steps. The apparent activation energies for the pyrolysis of WALO/PS mixture were in the range of 176 kJ mol⁻¹–369 kJ mol⁻¹ at various conversions of 1–100%. The effect of heating rate on the product distribution was studied. The carbon number distribution of the produced oil shifted slightly to light hydrocarbons with a decrease in heating rate. The selectivity of hydrocarbons corresponding to the styrene monomer was high for the pyrolysis of the WALO/PS mixture.     

Repolymerization of pyrolytic lignin for producing carbon fiber with improved properties

Lignin is a promising precursor of low-cost carbon fibers. However, the mechanical properties of carbon fibers produced from melt-spinning of raw lignin are poor, restricted by the randomly cross-linked polymer structures of lignin. In the present study, carbon fibers were produced from lignin-derived phenolic oil. Pyrolytic lignin was isolated from pyrolysis oil of red oak and washed with toluene to remove volatile impurities. Upon repolymerizing with 0.5% of sulfuric acid, the toluene-washed pyrolytic lignin became solid with the glass transition temperature (T_g) of 101 °C and the average molecular weight of 1267 Da. The repolymerized pyrolytic lignin was further processed into carbon fibers through melt-spinning, oxidative stabilization and carbonization at 1000 °C. The average tensile strength and modulus of the fibers were 855 MPa and 85 GPa, while the highest values of individual fibers were 1014 MPa and 122 GPa, respectively. The present study suggests that the quality of the carbon fiber produced from pyrolytic lignin could be further improved by process optimization.     

Impact of fast and slow pyrolysis on the degradation of mixed plastic waste: Product yield analysis and their characterization

This work primarily investigated the pyrolysis of post-consumer mixed plastic wastes during slow pyrolysis (non-isothermal) in a batch reactor to assess the effect of different heating rates on the product yield and its composition. The effect of residence time during fast pyrolysis (Isothermal) in Pyro-GC was also investigated. Initially, TG analysis was performed to investigate the degradation temperature range at different heating rates of 5, 10, 20 and 40 °C/min. Two different heating rates of 10 and 20 °C/min were selected for examining the effect on products such as oil and gases (H₂, CO, CO₂ and C₁-C₆ hydrocarbons) during slow pyrolysis. The oil obtained at higher heating rate had higher density (0.743 kg/m³) while the amount of residue decreased with the increase in heating rate. Also, the effect of residence time during fast pyrolysis was investigated using Pyro-GC at 500 °C for the product formation. It was observed that an optimum residence time of 10sec was favourable for the higher production of lower hydrocarbons (C₁-C₃) and less production of heavier hydrocarbons (C₆). This work represents the combined analysis of fast and slow pyrolysis and their impact on the product yield. Also, the effect of heating rate on non-isothermal condition and the effect of the residence time of volatiles in isothermal condition was analysed and reported.     

Hydrogen and methane production in extreme thermophilic conditions in two-stage (upflow anaerobic sludge bed) UASB reactor system

Two-stage hydrogen and methane production in extreme thermophilic (70 °C) conditions was demonstrated for the first time in UASB-reactor system. Inoculum used in hydrogen and methane reactors was granular sludge from mesophilic internal circulation reactor and was first acclimated for extreme thermophilic conditions. In hydrogen reactor, operated with hydraulic retention time (HRT) of 5 h and organic loading rate (OLR) of 25.1 kg COD/m³/d, hydrogen yield was 0.73 mol/mol glucose_added. Methane was produced in second stage from hydrogen reactor effluent. In methane reactor operated with HRT of 13 h and OLR of 7.8 kg COD/m³/d, methane yield was 117.5 ml/g COD_added. These results prove that hydrogen and methane can be produced in extreme thermophilic temperatures, but as batch experiments confirmed, for methane production lower temperature would be more efficient.     

Insights into pyrolysis and catalytic co-pyrolysis upgrading of biomass and waste rubber seed oil to promote the formation of aromatics hydrocarbon

To solve the problem of low aromatic hydrocarbon yield and selectivity in biomass catalytic pyrolysis, we used added oxygen-containing hydrogen supplier of rubber seed oil (RSO) with a higher hydrogen-to-carbon ratio to investigate the thermal decomposition behaviors, kinetic and production distribution of biomass, cellulose and RSO with the weight ratio of 1:2 using thermogravimetric analyzer (TGA) for kinetic analysis and fixed bed reactor with the feed composition of 1.2 g: 0.4 mL/min (Biomass to RSO) for product distribution in non-catalytic and catalytic co-pyrolysis over a HZSM-5 catalyst. The results show that there was a positive synergistic interaction between biomass and RSO according to the difference in weight loss, which could decrease the formation of solid coke at the end of experiment. The addition of the HZSM-5 catalyst can markedly increase the reaction activity, accelerate the reaction rate, and the reaction Ea, leading to a substantial increase in the conversion rate; furthermore, the residual carbon content will decrease, and the activations of Cellulose + RSO + Catalyst and Biomass + RSO + Catalyst are only 50.80 kJ/mol and 62.36 kJ/mol, respectively. The kinetic analysis showed that adding a catalyst did not change the decomposition mechanism. Co-pyrolysis of biomass and RSO could effectively improve the yield and selectivity of aromatics, when the pyrolysis temperature and catalytic temperature were 550 °C and 500 °C, respectively, the mass space velocity of RSO was 0.4 mL/min, the reaction time was 30min, the yields of benzene, toluene, xylene and ethyl benzene (BTXE) were up to 78.77%, and the selectivity of benzene, toluene and xylene was much better. Finally, the coke yield was substantially lower.     

Evaluating the effect of potassium on cellulose pyrolysis reaction kinetics

This paper proposes modifications to an existing cellulose pyrolysis mechanism in order to include the effect of potassium on product yields and composition. The changes in activation energies and pre-exponential factors due to potassium were evaluated based on the experimental data collected from pyrolysis of cellulose samples treated with different levels of potassium (0–1% mass fraction). The experiments were performed in a pyrolysis reactor coupled to a molecular beam mass spectrometer (MBMS). Principal component analysis (PCA) performed on the collected data revealed that cellulose pyrolysis products could be divided into two groups: anhydrosugars and other fragmentation products (hydroxyacetaldehyde, 5-hydroxymethylfurfural, acetyl compounds). Multivariate curve resolution (MCR) was used to extract the time resolved concentration score profiles of principal components. Kinetic tests revealed that potassium apparently inhibits the formation of anhydrosugars and catalyzes char formation. Therefore, the oil yield predicted at 500 ^°C decreased from 87.9% from cellulose to 54.0% from cellulose with 0.5% mass fraction potassium treatment. The decrease in oil yield was accompanied by increased yield of char and gases produced via a catalyzed dehydration reaction. The predicted char and gas yield from cellulose were 3.7% and 8.4%, respectively. Introducing 0.5% mass fraction potassium treatment resulted in an increase of char yield to 12.1% and gas yield to 33.9%. The validation of the cellulose pyrolysis mechanism with experimental data from a fluidized-bed reactor, after this correction for potassium, showed good agreement with our results, with differences in product yields of up to 5%.     

Oxidative pyrolysis of kraft lignin in a bubbling fluidized bed reactor with air

Fast pyrolysis of kraft lignin with partial (air) oxidation was studied in a bubbling fluidized bed reactor at reaction temperatures of 773 and 823 K. The bio-oil vapors were fractionated using a series of three condensers maintained at desired temperatures, providing a dry bio-oil with less than 1% water and over 96% of the total bio-oil energy.Oxygen feed was varied to study its effect on yield, composition, and energy recovery in the gas, char and oil products. The addition of oxygen to the pyrolysis process increased the production of gases such as CO and CO₂. It also changed the dry bio-oil properties, reducing its heating value, increasing its oxygen content, reducing its average molecular weight and tar concentration, while increasing its phenolics concentration. The lower reaction temperature of 773 K was preferred for both dry bio-oil yield and quality.Autothermal operation of the pyrolysis process was achieved with an oxygen feed of 72 or 54 g per kg of biomass at the reaction temperatures of 773 and 823 K, respectively. Autothermal operation reduced both yield and total energy content of the dry bio-oil, with relative reductions of 24 and 20% for the yield, 28 and 23% for the energy content, at 773 and 823 K.     

Characteristic of hydrogen and syngas evolution from gasification and pyrolysis of rubber

The characteristics of syngas evolution during pyrolysis and gasification of waste rubber have been investigated. A semi-batch reactor was used for the thermal decomposition of the material under various conditions of pyrolysis and high temperature steam gasification. The results are reported at two different reactor temperatures of 800 and 900 °C and at constant steam gasifying agent flow rate of 7.0 g/min and a fixed sample mass. The characteristics of syngas were evaluated in terms of syngas flow rate, hydrogen flow rate, syngas yield, hydrogen yield and energy yield. Gasification resulted in 500% increase in hydrogen yield as compared to pyrolysis at 800 °C. However, at 900 °C the increase in hydrogen was more than 700% as compared to pyrolysis. For pyrolysis conditions, increase in reactor temperature from 800 to 900 °C resulted in 64% increase in hydrogen yield while for gasification conditions a 124% increase in hydrogen yield was obtained. Results of syngas yield, hydrogen yield and energy yield from the rubber sample are evaluated with that obtained from woody biomass samples, namely hard wood and wood chips. Rubber gasification yielded more energy at the 900 °C as compared to biomass feedstock samples. However, less syngas and less hydrogen were obtained from rubber than the biomass samples at both the temperatures reported here.     

Utilization possibilities of palm shell as a source of biomass energy in Malaysia by producing bio-oil in pyrolysis process

Agriculture residues such as palm shell are one of the biomass categories that can be utilized for conversion to bio-oil by using pyrolysis process. Palm shells were pyrolyzed in a fluidized-bed reactor at 400, 500, 600, 700 and 800 °C with N₂ as carrier gas at flow rate 1, 2, 3, 4 and 5 L/min. The objective of the present work is to determine the effects of temperature, flow rate of N₂, particle size and reaction time on the optimization of production of renewable bio-oil from palm shell. According to this study the maximum yield of bio-oil (47.3 wt%) can be obtained, working at the medium level for the operation temperature (500 °C) and 2 L/min of N₂ flow rate at 60 min reaction time. Temperature is the most important factor, having a significant positive effect on yield product of bio-oil. The oil was characterized by Fourier Transform infra-red (FT-IR) spectroscopy and gas chromatography/mass spectrometry (GC-MS) techniques.     

Biocrude from biomass: pyrolysis of cottonseed cake

Fixed-bed pyrolysis experiments have been conducted on a sample of cottonseed cake to determine the possibility of being a potential source of renewable fuels and chemicals feedstocks, in two different reactors, namely a tubular and a Heinze retort. Pyrolysis atmosphere and pyrolysis temperature effects on the pyrolysis product yields and chemical composition have been investigated. The maximumm oil yield of 29.68% was obtained in N₂ atmosphere at a pyrolysis temperature of 550°C with a heating rate of 7°C min⁻¹ in a tubular reactor.     

Comparative study on pyrolysis characteristics and kinetics of oleaginous yeast and algae

The pyrolysis processes of oleaginous yeast and algae were studied and compared using a non-isothermal thermogravimetric analyzer at heating rates of 10–50 °C/min, and the most probable mechanism function and kinetic analyses of the main stage of pyrolysis were carried out by the Popuse method, Starink method, and Fridemen method. The main pyrolysis stage of the samples could be described by the Jander equation and Z–L–T equation and the activation energy of the three biomass was 108–117, 107–121 and 93–108 kJ/mol, respectively. For the three kinds of biomass, the DTG curves were divided based on the four pseudo-components by performing Gaussian fitting which are carbohydrates, proteins, lipids, others, and the weight coefficients of them could be identified. The activation energy of each pseudo-component was obtained in the range of 58.36–140.44 kJ/mol by the Kissinger method. The four-pseudo-component model based on Gaussian fitting provides effective data for the design of oleaginous yeast and algae thermal decomposition systems and the kinetic analysis of the pyrolysis process.