Production of low-sulfur fuels from catalytic pyrolysis of waste tires using formulated red mud catalyst.

Waste tires (WT) are produced in millions of tons per annum and their safe disposal is always a major environmental challenge because of fire hazards and the increasing cost of landfills. WT has high organic matter content that can be converted into fuels and chemicals if suitable technologies can be developed. Herein we report the in situ catalytic pyrolysis of WT using formulated red mud catalyst to produce low sulfur fuel that can be fractionated or can be used without fractionation. The in situ catalytic pyrolysis was conducted at 450-550 °C using formulated red mud catalyst. The yield of pyrolysis liquids ranged from 35 to 40 wt%. The liquid was very rich in limonene and long chain aliphatic hydrocarbons. The catalyst was effective in removing the sulfur compounds in the oil through reactive adsorption desulfurization mechanism. The sulfur species reacted with hematite, calcite, sodium hydroxide, and zinc oxide to form sulfides and were retained in the catalyst. The minimum sulfur content of the catalytic pyrolysis oil was 0.38 wt%. After catalyst regeneration in air through combustion, the catalyst activity was restored, and the catalyst was reused.

Environmentally Friendly New Catalyst Using Waste Alkaline Solution from Aluminum Production for the Synthesis of Biodiesel in Aqueous Medium.

Red mud (RM) is composed of a waste alkaline solution (pH = 13.3) obtained from the production of alumina. It contains high concentrations of hematite (Fe2O3), goethite (FeOOH), gibbsite [Al(OH)3], a boehmite (AlOOH), anatase (Tetragonal-TiO2), rutile (Ditetragonal dipyramidal-TiO2), hydrogarnets [Ca3Al2(SiO4)3-x(OH)4x], quartz (SiO2), and perovskite (CaTiO3). It was shown to be an excellent catalytic mixture for biodiesel production. To demonstrate the value of RM, an environmentally friendly process of transesterification in aqueous medium using waste cooking oil (WCO), MeOH, and waste alkaline solution (WAS) obtained from aluminum production was proposed. Triglycerides of WCO reacted with MeOH at 60 °C to yield mixtures of fatty acid methyl esters (FAMEs) in the presence of 0.019% (w/w) WAS/WCO using the WAS (0.204 mol L-1, predetermined by potentiometric titration) from aluminum production by the Bayer process. The use of the new catalyst (WAS) resulted in a high yield of the products (greater than 99% yield).

From Biomass to Fuel Blendstocks via Catalytic Fast Pyrolysis and Hydrotreating: An Evaluation of Carbon Efficiency and Fuel Properties for Three Pathways.

Biomass was upgraded to fuel blendstocks via catalytic fast pyrolysis (CFP) followed by hydrotreating using three approaches: ex situ CFP with a zeolite catalyst (HZSM-5), ex situ CFP with a hydrodeoxygenation catalyst (Pt/TiO2) and cofed hydrogen, and in situ CFP with a low-cost mixed metal oxide catalyst (red mud). Each approach was evaluated using a common pine feedstock and the same hydrotreating procedure. The oxygen contents in the CFP oils ranged from 17 to 28 wt % on a dry basis, and the carbon efficiencies for the CFP processes were in the range of 28-38%. The residual oxygen was reduced to <1 wt % during hydrotreating, which was operated for 104-140 h for each CFP oil without plugging issues. The hydrotreating carbon efficiencies were 81-93%. The CFP pathway with the hydrodeoxygenation catalyst gave the highest overall carbon efficiency from biomass to fuel blendstocks (34%) but, at the same time, also the highest cumulative hydrogen consumption during CFP and hydrotreating. The zeolite pathway produced the largest fraction boiling in the gasoline range and the highest estimated octane number due to the high aromatic content in that CFP oil. The in situ red mud pathway produced the largest fraction of diesel-range products with the highest derived cetane number. However, advances in the CFP and hydrotreating process are required to improve the fuel blendstock properties for all pathways.

Ethanol production of semi-simultaneous saccharification and fermentation from mixture of cotton gin waste and recycled paper sludge.

Ethanol production from the steam-exploded mixture of 75% cotton gin waste and 25% recycled paper sludge in various conditions was investigated by semi-simultaneous saccharification and fermentation (SSSF) consisting of a pre-hydrolysis and a simultaneous saccharification and fermentation (SSF). Four cases were studied: 24-h pre-hydrolysis + 48-h SSF (SSSF 24), 12-h pre-hydrolysis + 60-h SSF (SSSF 12), 72-h SSF, and 48-h hydrolysis + 24-h fermentation (SHF). The ethanol concentration, yield, and productivity of SSSF 24 were higher than those of the other operations. A model of SSF was used to simulate the data for four components in SSF. The analysis of the reaction rates of cellobiose, glucose, cell, and ethanol using the model and the parameters from the experiments showed that there was a transition point of the rate-controlling step at which the cell growth control in the initial 2 h was changed to the cellobiose reaction control in later period during ethanol production of SSF from the mixture.

Prospective contributions of biomass pyrolysis to China's 2050 carbon reduction and renewable energy goals.

Recognizing that bioenergy with carbon capture and storage (BECCS) may still take years to mature, this study focuses on another photosynthesis-based, negative-carbon technology that is readier to implement in China: biomass intermediate pyrolysis poly-generation (BIPP). Here we find that a BIPP system can be profitable without subsidies, while its national deployment could contribute to a 61% reduction of carbon emissions per unit of gross domestic product in 2030 compared to 2005 and result additionally in a reduction in air pollutant emissions. With 73% of national crop residues used between 2020 and 2030, the cumulative greenhouse gas (GHG) reduction could reach up to 8620 Mt CO2-eq by 2050, contributing 13-31% of the global GHG emission reduction goal for BECCS, and nearly 4555 Mt more than that projected for BECCS alone in China. Thus, China's BIPP deployment could have an important influence on achieving both national and global GHG emissions reduction targets.

Biomethanation of invasive water hyacinth from eutrophic waters as a post weed management practice in the Dominican Republic: a developing country.

Anaerobic digestion of water hyacinth (Pontederia crassipes Mart.) from eutrophic water bodies could be a sustainable post weed management practice to generate bioenergy. Comparative analyses of the water quality, physicochemical characteristics, and biomethanation kinetics of water hyacinth from two sites with different water types (brackish versus freshwater) in the Ozama river, Dominican Republic, were conducted. Also, the energy produced from the anaerobic digestion and that consumed in harvesting was estimated. The highest non-structural components in the form of protein (18.8 ± 1.9%) and extractives (26.4 ± 0.1%) were found in brackish water hyacinth, whereas that from freshwater had the highest amount of holocellulose (41.2 ± 2.8%). Indicators of plant productivity, i.e., chlorophyll b and bulk density, were more than 30% higher in brackish than in freshwater hyacinth. The methane production rate in the digestion of water hyacinth from brackish water (22.5 N. L/kg VS added· day) was twice that from freshwater (10.0 N. L/kg VSadded· day). The higher nutrient content in the brackish water could have influenced the superior performance of water hyacinth from that source compared with that from freshwater. Overall, the maximum methane potential of the Ozama river water hyacinth was 399.2 ± 32.2 N. L CH4/kg VSadded. The estimated energy produced per ton of fresh biomass was 846.5 MJ, but only 57.9 MJ would be required for mechanical harvesting. The biomethanation of water hyacinth can mitigate weed management costs in developing countries.

Assessment of upgrading ability and limitations of slow co-pyrolysis: Case of olive mill wastewater sludge/waste tires slow co-pyrolysis.

Olive mill wastewater sludge (OMWS) and waste tires (WTs), abundant wastes in Tunisia, were used as feedstock in a slow co-pyrolysis pilot reactor to produce upgraded pyrolytic oil as an alternative fuel. Despite the improvement of some properties of the pyrolytic oil when waste tires were added in the feed blend, a negative synergy was observed in the yield of the oil compared with that of char. The characterization of oil samples showed synergetic interaction between OMWS and WTs during co-pyrolysis which led to a partial deoxygenation and resulted in reduction of viscosity and increase in the calorific value of the co-pyrolytic oils. However, the co-pyrolytic oil properties did not meet the requirements of commercial diesel and will need further improvement by effective standardization to meet marketable specifications. Compared with catalytic fast pyrolysis (CFP) followed by hydrodeoxygenation (HDO), OMWS/WTs slow co-pyrolysis showed some limitations but it can be considered as a simple, clean and cheap process upgrading technique for bio-oil production (∼40% lower in fixed capital investment and ∼30% lower in fuel selling price).

The conversion of biomass to light olefins on Fe-modified ZSM-5 catalyst: Effect of pyrolysis parameters.

Light olefins are the key building blocks for the petrochemical industry. In this study, the effects of in-situ and ex-situ process, temperature, Fe loading, catalyst to feed ratio and gas flow rate on the olefins carbon yield and selectivity were explored. The results showed that Fe-modified ZSM-5 catalyst increased the olefins yield significantly, and the ex-situ process was much better than in-situ. With the increasing of temperature, Fe-loading amount, catalyst to feed ratio, and gas flow rate, the carbon yields of light olefins were firstly increased and further decreased. The maximum carbon yield of light olefins (6.98% C-mol) was obtained at the pyrolysis temperature of 600°C, catalyst to feed ratio of 2, gas flow rate of 100ml/min, and 3wt% Fe/ZSM-5 for cellulose. The selectivity of C2H4 was more than 60% for all feedstock, and the total light olefins followed the decreasing order of cellulose, corn stalk, hemicelluloses and lignin.

Pyrolysis characteristics and kinetics of chicken litter.

Chicken litter generally consists of a mixture of bedding, manure, feathers and spilled food. Flock of birds litter (flock) is a litter consisting of hardwood shavings, feed, feathers and manure; and broiler litter (broiler) is a cake of chicken litter. A kinetic investigation of the pyrolysis of chicken litter (flock and broiler) was carried out using thermogravimetric analysis (TGA) at heating rates of 5 degrees C/min, 10 degrees C/min and 20 degrees C/min. Most of the materials decomposed between 270 degrees C and 590 degrees C at each heating rate. The region of decomposition of flock and broiler was slightly lower than that of the wood chips. Wood chips (bedding material) decomposed in two stages, while flock and broiler decomposed in three stages. Apparent activation energies increased from 99 to 484 kJ/mol for the three samples when the pyrolytic conversion increased from 5% to 95%.

Hydraulic retention time effects on wastewater nutrient removal and bioproduct production via rotating algal biofilm reactor.

Rotating algal biofilm reactor (RABR) technology was successfully employed in an effective strategy to couple the removal of wastewater nutrients with accumulation of valuable bioproducts by grown algae. A secondary stage municipal wastewater was fed to the developed system and the effects of the hydraulic retention time (HRT) parameter on both nutrient removal and bioproduct production were evaluated under fed-batch operation mode. Two sets of bench scale RABRs were designed and operated with HRTs of 2 and 6days in order to provide competitive environment for algal growth. The HRT significantly affected nitrogen and phosphorus uptakes along with lipid and starch accumulations by microalgae in harvested biofilms. Domination of nitrogen removal in 2-day HRT with higher lipid accumulation (20% on dried weight basis) and phosphorus removal in 6-day HRT with higher starch production (27% on dried weight basis) was observed by comparing the performances of the RABRs in duplicate runs.

Microbubble assisted polyhydroxybutyrate production in Escherichia coli.

BACKGROUND: One of the potential limitations of large scale aerobic Escherichia coli fermentation is the need for increased dissolved oxygen for culture growth and bioproduct generation. As culture density increases the poor solubility of oxygen in water becomes one of the limiting factors for cell growth and product formation. A potential solution is to use a microbubble dispersion (MBD) generating device to reduce the diameter and increase the surface area of sparged bubbles in the fermentor. In this study, a recombinant E. coli strain was used to produce polyhydroxybutyrate (PHB) under conventional and MBD aerobic fermentation conditions. RESULTS: In conventional fermentation operating at 350 rpm and 0.8 vvm air flow rate, an OD600 of 6.21 and PHB yield of 23 % (dry cell basis) was achieved. MBD fermentation with similar bioreactor operating parameters produced an OD600 of 8.17 and PHB yield of 43 % PHB, which was nearly double that of the conventional fermentation. CONCLUSIONS: This study demonstrated that using a MBD generator can increase oxygen mass transfer into the aqueous phase, increasing E. coli growth and bioproduct generation.

Composition and ethanol production potential of cotton gin residues.

Cotton gin residue (CGR) collected from five cotton gins was fractionated and characterized for summative composition. The major fractions of the CGR varied widely between cotton gins and consisted of clean lint (5-12%),hulls (16-48%), seeds (6-24%), motes (16-24%), and leaves (14-30%). The summative composition varied within and between cotton gins and consisted of ash (7.9-14.6%), acid-insoluble material (18-26%), xylan (4-15%),and cellulose (20-38%). Overlimed steam-exploded cotton gin waste was readily fermented to ethanol by Escherichia coli KO11. Ethanol yields were feedstock and severity dependent and ranged from 58 to 92.5% of the theoretical yields. The highest ethanol yield was 191 L (50 gal)/t, and the lowest was 120 L (32 gal)/t.

Thermogravimetric analysis and fast pyrolysis of Milkweed.

Pyrolysis of Milkweed was carried out in a thermogravimetric analyzer and a bubbling fluidized bed reactor. Total liquid yield of Milkweed pyrolysis was between 40.74% and 44.19 wt% between 425 °C and 550 °C. The gas yield increased from 27.90 wt% to 33.33 wt% with increasing reaction temperature. The higher heating values (HHV) of the Milkweed bio-oil were relatively high (30.33-32.87 MJ/kg) and varied with reaction temperature, feeding rate and fluidization velocity. The selectivity for CO2 was highest within non-condensable gases, and the molar ratio of CO2/CO was about 3 at the different reaction conditions. The (13)C NMR analysis, of the bio-oil showed that the relative concentration carboxylic group and its derivatives was higher at 425 °C than 475 °C, which resulted in slightly higher oxygen content in bio-oil. The pH of aqueous phase obtained at 475 °C was 7.37 which is the highest reported for any lignocellulosic biomass pyrolysis oils.

Thermogravimetric and kinetic study of Pinyon pine in the various gases.

As a renewable resource, Pinyon pine can be converted into bio-oil, gas, and char through pyrolysis. It is known that recycling of the non-condensable gases, which are produced by fast pyrolysis, can increase liquid yield and decrease char yield. In this study, pyrolysis characteristics and kinetics of Pinyon pine were investigated in TGA using simulated non-condensable gases (N2, H2/N2, H2/CO2, and He/CO/H2). The apparent activation energy of Pinyon pine increased from 43.9 to 160.3kJ mol(-1) with increasing pyrolysis conversion from 5% to 95% in pure nitrogen, and reaction order was 1.35. When hydrogen (H2) and carbon monoxide (CO) mixtures were used as simulated gases, the maximum degradation temperature and activation energy decreased by 4-11°C and 6.1-10.2kJ/mol, respectively. The results show that recycling of non-condensable gases could positively influence the fast pyrolysis of biomass.

Storage stability of biocrude oils from fast pyrolysis of poultry litter.

The unstable nature of biocrude oils produced from conventional pyrolysis of biomass is one of the properties that limits its application. In the disposal of poultry litter via pyrolysis technology, the biocrude oil produced as a value-added product can be used for on farm applications. In this study, we investigated the influence of bedding material (wood shavings) on the storage stability of biocrude oils produced from the fast pyrolysis of poultry litter. The biocrude oils produced from manure, wood (pine and oak), and mixtures of manure and wood in proportions (75:25 50:50, and 25:75w/w%) were stored under ambient conditions in sealed glass vials for a period of 6 months and their stability were monitored by measuring the changes in viscosity over time. The manure oil had the lowest rate of viscosity change and thus was relatively the most stable and the oils from the 50:50w/w% litter mixtures were the least stable. The rate of viscosity change of the manure biocrude oil was 1.33cP/day and that of the 50/50 litter mixture was 7.6cP/day for pine and 4.17cP/day for oak. The spectrometric analyses of the biocrude oils showed that the presence of highly reactive oxygenated functionalities in the oil were responsible for the instability characteristic of the litter biocrude oils. The poor stability of the biocrude oil from the 50:50w/w% litter mixtures was attributed to reactions between nitrogenous compounds (amides) from protein degradation and oxygenated compounds from the decomposition of polysaccharides and lignin. The addition of 10% methanol and 10% ethanol to the oil from 50% manure and 50% pine reduced the initial viscosity of the oil and was also beneficial in slowing down the rate of viscosity change during storage.

The operable modeling of simultaneous saccharification and fermentation of ethanol production from cellulose.

An operable batch model of simultaneous saccharification and fermentation (SSF) for ethanol production from cellulose has been developed. The model includes four ordinary differential equations that describe the changes of cellobiose, glucose, yeast, and ethanol concentrations with respect to time. These equations were used to simulate the experimental data of the four main components in the SSF process of ethanol production from microcrystalline cellulose (Avicel PH101). The model parameters at 95% confidence intervals were determined by a MATLAB program based on the batch experimental data of the SSF. Both experimental data and model simulations showed that the cell growth was the rate-controlling step at the initial period in a series of reactions of cellulose to ethanol, and later, the conversion of cellulose to cellobiose controlled the process. The batch model was extended to the continuous and fed-batch operating models. For the continuous operation in the SSF, the ethanol productivities increased with increasing dilution rate, until a maximum value was attained, and rapidly decreased as the dilution rate approached the washout point. The model also predicted a relatively high ethanol mass for the fed-batch operation than the batch operation.

Influence of pine wood shavings on the pyrolysis of poultry litter.

Poultry litter from broilers and turkeys are a mixture of manure, feathers, feed and wood shavings, thus pyrolysis oils produced from this material are influenced by the individual components. In order to determine the influence of wood shavings that are used as bedding material, we investigated the pyrolysis of pine wood shavings and poultry manure. Because manure from layer chickens are usually not contaminated with wood shavings, we made mixtures of layer manure and pine wood shavings in the following manure to wood ratios, 100:0, 75:25, 50:50, 25:75, and 0:100 w/w and pyrolyzed them in a fluidized bed reactor at 450 °C. The total liquid yield ranged from 43.3 to 62.7 wt.%. The layer manure oil had a HHV of 29.7 MJ/kg and pH of 5.89 compared to pine wood oil which had HHV of 25.6 MJ/kg and pH of 3.04. The addition of wood shavings to manure clearly influenced the physical properties of the oil, resulting in a decrease in pH and HHV and an increase in density. The oils had relatively high nitrogen content ranging from 1.36 to 5.88 wt.%. The ash (<0.07 wt.%) and sulfur (<0.28 wt.%) contents were very low. FTIR, (13)C NMR and (1)H NMR spectrometric analysis of the oils showed that manure oil was rich in hydrocarbons and nitrogenous compounds such as primary, secondary amides, aromatic amines and N-heterocyclic. The properties of the oils were strongly influenced by the amount of wood in the mixture.