The percentage of expandable layers in illite/smectite (I/S) mixed-layer clay decreases with increasing temperature and depth in a section through marine Cretaceous shales in the Champlin 1 Hartley Federal well in the Powder River basin, Wyoming. This systematic change in I/S expandability is evidence that low-expandable I/S in Cretaceous shales of the northern Rocky Mountain area reflects, at least in part, thermal alteration during burial diagenesis. In eastern Montana and western North Dakota where I/S in the Lower Cretaceous Mowry and Skull Creek source rocks is diagenetically unaltered, only trace amounts of hydrocarbons have been found in the Lower Cretaceous and other Cretaceous sandstones. Elsewhere in the northern Rocky Mountain-Great Plains region, hydrocarbons in the Lower Cretaceous Muddy Sandstone and its equivalents occur within or immediately adjacent to areas in which I/S clay in the Mowry and Skull Creek shales has been diagenetically altered during burial. Altered I/S and thermally mature organic matter, as defined by Rock-Eval pyrolysis values, coexist in these source rocks. Both may be used as maturation indicators in the search for Cretaceous-source hydrocarbons in the northern Rocky Mountain area.

The kinetic characteristics of crude oil pyrolysis experiments form the basis for quantitative analysis of shale oil content in Rock-Eval pyrolysis experiments. To study the thermal evaporation kinetics of crude oil in shale, pyrolysis experiments of whole source rock sample and post-extracted sample were carried out on Rock-Eval 6 with the heating rates of 5, 15 and 25°C min−1, respectively. The thermal evaporation of crude oil can be described using a parallel first-order reaction model. A simple method for calculating the kinetic characteristics of the thermal evaporation of extracted crude oil is proposed.

Although the awareness of the environmental damage caused by plastic pollution has recently increased, few steps have been taken to confront its consequences. These consequences are often most severe in the Global South where countries often lack proper waste management infrastructure. Unless the market value of plastic waste increases, it will simply be discarded, eventually making its way to the environment. It has been established that polyolefin plastic can be converted to a sulfur-free fuel oil by pyrolysis, suitable for use in diesel engines or as a clean cooking fuel. However, carrying out this chemistry in the Global South is challenging. Any process intended for use in the Global South must be safe, robust, efficient, simple to operate, low cost, and most importantly profitable for the operator. When the average daily wage in sub-Saharan Africa is less than 3 USD, an income provided from plastic waste fuel can be significant. The research presented herein focuses on the optimization of a plastic-to-fuel processor that can be built using the principles of appropriate technology. The results of this optimization and profitability assessment will be described. This research has been conducted in collaboration with the NGOs Empowered Solutions for Environmental Sustainability and UpCycle Africa.

Biochar is considered a promising option for the development of sustainable agroecosystems, due to its diverse agronomic and environmental benefits. In this context, the aim of this study was to carry out a bibliometric analysis on biochar research in Brazil within an agricultural context, including investigating the raw materials most employed for its production in the country. The analysis was conducted based on a search for scientific articles (peer-reviewed papers) at the Web of Science database (WoS Core Collection) from 2003 to 2020 specifically in Brazil. A performance analysis was carried out by applying a descriptive and metric approach concerning research constituents (authors, institutions, countries and keywords) and science mapping to clarify scientific collaborations and cognitive and intellectual structure patterns regarding the biochar domain in Brazilian research, using the VOSviewer software. The obtained studies were also analyzed individually to classify the different raw materials employed in biochar production. A total of 261 scientific articles met the screening criteria, indicating that the beginning of biochar publications in Brazil took place in 2003, increasing until 2015 and peaking in 2021. Institutions and authors with the highest publication contributions were the Brazilian Agricultural Research Corporation (EMBRAPA) (Novotny E.), São Paulo University (USP) (Cerri C.) and Federal Lavras University (UFLA) (Melo L.). The United States, Spain, Australia, Germany and the Netherlands present the most collaborations on biochar research with Brazil. The biochar domain was highly associated with the following keywords: biochar, pyrogenic carbon, pyrolysis, charcoal, immobilization, black carbon, soil fertility and soil and characterization. Raw materials of plant origin were the most employed in biochar research in Brazil, with wood residues being the most studied and residues originated from the sugar-energy industry (straw, bagasse and filter cake) identified as exhibiting high potential for future studies. Poultry litter is the most promising animal waste for biochar production, while the use of biosolids can be innovative, contributing to the consolidation of biochar as an option for serious urban waste sanitary management problems.

Wasted tires are the great source of fuel and valuable components but could be a cause of environmental and land pollution. This study shows the detailed method for the determination of radiocarbon isotope (14C) concentration in tires and their pyrolysis products. Samples are taken from truck and passenger car tires in the form of shredded rubber, pyrolysis oil and recovered carbon black. Liquid scintillation counting (LSC) and accelerator mass spectrometry (AMS) techniques were used for the investigation at Gliwice Radiocarbon and Mass Spectrometry Laboratory, and National Laboratory for Age Determination, Trondheim, Norway. The results are in good agreement. Radiocarbon concentration of the rubber varies significantly because of its complex structure and composition within the tires. The 14C concentration values were found to be higher in pyrolytic oil compared to rubber, and greater in truck tires rather than car tires.

Applying coffee pulp biochar (BC) can be a complementary practice to the application of chemical fertilizers (CF) of crops; however, little evidence of its combined effects on coffee cultivation has been reported. A field trial was carried out during two evaluation years (2019 and 2020) to analyse the effect of the application of different BC doses (0, 4, 8 and 16 t/ha) in combination with four levels of fertilization (0, 33, 66 and 100% of the nutritional requirements) on physiological responses of 3-year-old coffee (Coffea arabica L. var. Castillo) trees. The results indicated that trees with 0 t/ha BC and 0% CF showed the lowest values in all the physiological variables studied (gs = 269.9 and 126.8 mmol/m2/s; Chl = 61.7 and 54.7 At-leaf readings; yield = 0.21 and 0.22 kg of dry parchment coffee (DPC)/tree for 2019 and 2020, respectively). Coffee trees treated with 8 t/ha BC and CF levels of 100% registered the highest results in gs (424.9 and 366.9 mmol/m2/s), Chl (71.1 and 69.8 At-leaf readings), yield (0.41 and 0.57 kg of DPC/tree) in 2019 and 2020, respectively. In conclusion, the application of BC from coffee pulp, especially at a dose of 8 t/ha, generates a positive effect on yield, gs, leaf nutrient concentration and Chl of coffee trees. The use of BC can be an alternative to complement the mineral nutrition of commercial coffee crops to help reduce the application of CF.

Wood vinegar, a product of pyrolysis, can induce phytotoxicity on plants when applied at an adequate rate and concentration. The objective of this research was to investigate wood vinegar obtained from the pyrolysis of apple tree branches for weed control in dormant zoysiagrass. In environment-controlled growth chambers, white clover visual injury and shoot mass reduction were evaluated and compared to the nontreated control after wood vinegar application at 1,000, 2,000, or 4,000 L ha−1 under 10 C or 30 C temperature conditions. Averaged across rates, wood vinegar rapidly desiccated white clover and caused 83% and 71% visual injury at 10 C and 30 C, respectively, at 1 d after treatment (DAT). Averaged across temperatures, wood vinegar at 1,000, 2,000, and 4,000 L ha−1 reduced white clover shoot mass by 56%, 81%, and 98% from the nontreated control at 10 DAT, respectively. In field experiments, weed control increased as wood vinegar rates increased from 1,000 to 5,000 L ha−1 in dormant zoysiagrass. The effective application dose of wood vinegar required to provide 90% control (ED90) of annual fleabane, Persian speedwell, and white clover was determined to be 2,450, 2,300, and 4,020 L ha−1, respectively, at 2 wk after treatment. Turf quality did not differ among the wood vinegar treatments and the nontreated control when zoysiagrass completely recovered from dormancy. Overall, results illustrate that wood vinegar resulting from the pyrolysis of apple tree branches can be used as a nonselective herbicide in dormant turfgrass, offering a new nonsynthetic herbicide option for weed control in managed turf.

Plastics generally play a very important role in a plethora of industries, fields and our everyday lives. In spite of their cheapness, availability and important contributions to lives, they however, pose a serious threat to the environment due to their mostly non-biodegradable nature. Recycling into useful products can reduce the amount of plastic waste. Thermal degradation (Pyrolysis) of plastics is becoming an increasingly important recycling method for the conversion of plastic materials into valuable chemicals and oil products. In this work, waste Polyethylene terephthalate (PET) water bottles were thermally converted into useful gaseous and liquid products. A simple pyrolysis reactor system has been used for the conversions with the liquid product yield of 65 % at a temperature range of 400°C to 550°C. The chemical analysis of the pyrolytic oil showed the presence of functional groups such as alkanes, alkenes, alcohols, ethers, carboxylic acids, esters, and phenyl ring substitution bands. The main constituents were 1-Tetradecene, 1-Pentadecene, Cetene, Hexadecane, 1-Heptadecene, Heptadecane, Octadecane, Nonadecane, Eicosane, Tetratetracontane, 1-Undecene, 1-Decene). The results are promising and can be maximized by additional techniques such as hydrogenation and hydrodeoxygenation to obtain value-added products.

The excessive use of plastic, especially polystyrene (PS), has caused serious environmental pollution. The efficient utilization of plastics and the conversion of plastics into value-added carbon materials are the concerns of researchers. Herein, we propose novel “pyrolysis–deposition” method to convert one popular plastic substance, PS, into ordered mesoporous carbons (OMCs). During the synthesis process, PS is pyrolyzed into small organic gases under high temperature, which is then adsorbed through capillary adsorption into the mesoporous of SBA-15 in the presence of catalyst. The obtained OMCs have high specific surface area, uniform pore size, and ordered pore structure. The OMCs exhibit specific capacitance of 118 F/g at a current density of 0.2 A/g and electrochemical stability of 87.2% at a current density of 2 A/g after 5000 cycles. The pyrolysis–deposition strategy provides a new idea to convert waste plastics into high-performance carbon materials for electrochemical applications.

Glassy carbon nanolattices can exhibit very high strength-to-weight ratios as a consequence of their small size and the material properties of the constituent material. Such nanolattices can be fabricated by pyrolysis of polymeric microlattices. To further elucidate the influence of the mechanical size effect of the constituent material, compression tests of glassy carbon nanopillars with varying sizes were performed. Depending on the specific initial polymer material and the nanopillar size, varying mechanical properties were observed. Small nanopillars exhibited elastic-plastic deformation before failure initiation. Moreover, for smaller nanopillars higher strength values were observed than for larger ones, which might be related to smaller defects and a lower defect concentration in the material.

CP (Cetylpyridinium)-exchanged smectite was manufactured by the cationic exchange reaction of Na-smectite with CP. The adsorption behaviour shows a typical L-type isotherm representing continuous and stable adsorption in excess of twice the cation exchange capacity of CP. CP-smectite shows a strong interlayer (d001) expansion to 40.2 Å when an amount of CP equivalent to 140% of the CEC is exchanged into smectite. CP-smectite is characterized by strong alkalinity (pH 9.3), low swelling (4.5 ml/2 g), low viscosity (3.9 mPa s), and strong and fast flocculation. These characteristics are in striking contrast to Na-smectite except for the alkalinity. CP-smectite shows no signs of desorption of the organic species under varying pH conditions (pH 2–12). Desorption is slight even when washed three times with DH2O (distilled water). Pyrolysis of CP-smectite begins at 250°C and ends at 400°C. These stable and persistent characteristics and the relatively low price of CP point to the likely increased use of CP-smectite as an organoclay.

Boron carbide (B4C) is an attractive material for numerous applications including vehicle armor, cutting tools, blasting nozzles, and abrasive powder, owing to its extreme hardness, high melting point, high Young’s modulus, and excellent thermoelectric properties. However, the application of B4C is limited by the high-temperature synthesis process. The present work aims to explore a low-temperature manufacturing process for synthesizing B4C with a small amount of free carbon. Poly(resorcinol borate) with an aromatic structure and high char yield was chosen as the aromatic polymeric precursor. A combination of Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Raman spectroscopy was performed to investigate the influences of the reaction temperature and holding time on the changes in the precursor microstructure. The results indicate that the rod-like structure of crystalline B4C is successfully synthesized at 600 °C, and the free carbon can be reduced to about 0.8 wt% in the final product. This is because the pyrolysis temperature controlled the carbon content of the B4C, which led to an enlarged contact domain between B2O3 and carbon, and a relatively low-temperature synthesis of B4C.

Organic gels obtained by sol–gel polycondensation reaction followed by subcritical drying in ambient conditions are termed as xerogels which are pyrolyzed to yield carbon xerogels. Resorcinol formaldehyde (RF) derived carbon xerogels have received considerable attention due to their higher carbon yield and ease of tuning their microstructure and therefore physiochemical properties. Recent advances in the synthesis of carbon xerogels have allowed porous as well as non-porous but large external surface area morphologies. Further efforts have been made about increasing the surface area by activation or changing the microstructure by doping with foreign elements. These advances in the area of carbon xerogels synthesis led to their use as high performance anode materials for Li ion batteries recently. This review summarizes these recent studies on electrochemical performance of carbon xerogels to clearly demonstrate their potential as high capacity anode material for Li ion batteries. Notably, given the potential not only for Li ion batteries but also for latest sodium-ion batteries and super-capacitors, this review provides a much needed attention of scientific community to so far unnoticed carbon xerogel materials.

Government support uncertainty, scarce yield information, and the inherent risk in bioeconomic phenomena are some of the deterrents faced by investors in the nascent cellulosic biofuel industry. A financial probabilistic model was developed to contrast the economic feasibility of producing cellulosic biofuels from energy cane and sweet sorghum using three technologies: hydrolysis, pyrolysis, and gasification. Hydrolysis and pyrolysis proved feasible (showed possibilities of a positive net present value) without government support and conditioned to stochastic feedstock yields and biofuel prices. Gasification was feasible with government support. Improved feedstock and biofuel productivity would considerably raise the feasibility probabilities for hydrolysis and pyrolysis without government support.

The continued use of finite fossil fuel resources has shifted thinking toward a potential future bioeconomy, and the field of polymer science will play a critical role in valorization of bio-derived materials. Interest in renewable resources is constantly increasing, backed up by new environmental regulations and economic considerations. Biomass is abundant and diverse, and polymeric materials based on renewable feedstocks represent a viable alternative to fossil resources. Bio-oil—a dark brown, free-flowing organic liquid mixture—is a product of fast pyrolysis or liquefaction of biomass. Bio-oil generally comprises a large amount of water and hundreds of organic chemical compounds that can be further broken down into families of reactive structures, capable of producing new synthetic pathways to design and synthesize high-performance biopolymers and bioresins using lignocellulosic biomass. These new polymeric materials have demonstrated a unique combination of thermal resistance and low cost intrinsic of the biomass utilized, as well as superior mechanical performance of polymeric resins sufficient to compete with high-performance structural resins and coating materials.

The synthesis technique that can be used to accelerate the discovery of materials for various energy conversion and storage applications is presented. Specifically, this technique allows a rapid and controlled synthesis of mixed metal oxide particles using plasma oxidation of liquid droplets containing mixed metal precursors. The conventional wet chemical methods for synthesis of multimetal oxide solid solutions often require time-consuming high pressure and temperature processes, and so the challenge is to develop rapid and scalable techniques with precise compositional control. The concept is demonstrated by synthesizing binary and ternary transition metal oxide solid solutions with control over entire composition range using metal precursor solution droplets oxidized using atmospheric oxygen plasma. The results show the selective formation of metastable spinel and the rocksalt solid solution phases with compositions over the entire range by tuning the metal precursor composition. The synthesized manganese doped nickel ferrite nanoparticles, NiMn z Fe2−z O4 (0 ≤ z ≤ 1), exhibits considerable electrocatalytic activity toward oxygen evolution reaction, achieving an overpotential of 0.39 V at a benchmarking current density of 10 mA/cm2 for a low manganese content of z = 0.20.

First-generation grain ethanol biofuel has affected the historical excess capacity problem in U.S. agriculture. Second-generation cellulosic ethanol biofuel has had difficulty achieving cost-competitiveness. Third-generation drop-in biofuels are under development. If lignocellulosic biomass from perennial grasses becomes the feedstock of choice for second- and third-generation biorefineries, an integrated system could evolve in which a biorefinery directly manages feedstock production, harvest, storage, and delivery. Modeling was conducted to determine the potential economic benefits from an integrated system. Relatively low-cost public policies that could be implemented to facilitate economic efficiency are proposed.

Zinc oxide thin films prepared by sol-gel and doped with different aluminum percentages were deposited by spray-pyrolysis deposition techniques on FTO and ITO substrates. The films were applied as the sensitive layer of pH-sensors EGFET devices. ZnO:Al films on FTO substrates shows a decrease in sensor quality with the dopant percentage increase. The opposite occurs when the substrate was ITO. The best quality film to be used as pH-sensor on FTO substrates was the ZnO:Al (3%) with 29 mV/pH sensitivity value and linear adjust of 0.99. For ITO substrates the best quality was achieved for ZnO:Al (10%), with sensitivity about 30 mV/pH and 0.99 linear adjust.

Thermal analysis techniques are routinely applied to characterize the thermal behavior of metal organic precursors used for oxide film preparation. Since the mass of films is very low, researchers do their thermal analyses on powders and consider that the results are representative of films. We will show here that, in general, this assumption is not true. Several examples involving precursors of YBa2Cu3O7-x (Ba and Y trifluoroacetates and Ba propionate) will serve to appreciate that films can behave very differently than powders due to their enhanced heat and mass transport paths. Ultimately, we will demonstrate that, in some cases, relying on powders thermal analysis may lead to erroneous conclusions.