Search

Structural properties of carbonized cellulose were explored to conjugate the outcomes from various characterization techniques, namely X-ray diffraction (XRD), Raman spectroscopy, and high-resolution transmission electron microscopy. All these techniques have evidenced the formation of graphene stacks with a size distribution. Cellulose carbonized at 1000 and 1800 °C at a heating rate of 2 °C/min showed meaningful differences in Raman spectroscopy, whereas in XRD, the differences were not well pronounced, which implies that the crystallite sizes calculated by each technique have different significations. In the XRD patterns, the origin of a specific feature at a low scattering angle commonly reported in the literature but poorly explained so far, was identified. The different approaches used in this study were congruous in explaining the observations that were made on the cellulose-derived carbon samples. The remnants of the basic structural unit (BSU) are developed during primary carbonization. Small graphene-based crystallites inherited from the BSUs, which formerly developed during primary carbonization, were found to coexist with larger ones. Even if the three techniques give information on the average size of graphenic domains, they do not see the same characteristics of the domains; hence, they are not identical, nor contradictory but complementary. The arguments developed in the work to explain which characteristics are deduced from the signal obtained by each of the three characterization techniques relate to physics phenomena; hence, they are quite general and, therefore, are valid for all kind of graphenic materials. [ABSTRACT FROM AUTHOR]

In this paper, gas permeability studies were performed on materials based on natural rubber/acrylonitrile butadiene rubber blends and nanoclay incorporated blend systems. The properties of natural rubber (NR)/nitrile rubber (NBR)/nanoclay nanocomposites, with a particular focus on gas permeability, are presented. The measurements of the barrier properties were assessed using two different gases-O 2 and CO 2 -by taking in account the blend composition, the filler loading and the nature of the gas molecules. The obtained data showed that the permeability of gas transport was strongly affected by: (i) the blend composition-it was observed that the increase in acrylonitrile butadiene rubber component considerably decreased the permeability; (ii) the nature of the gas-the permeation of CO 2 was higher than O 2 ; (iii) the nanoclay loading-it was found that the permeability decreased with the incorporation of nanoclay. The localization of nanoclay in the blend system also played a major role in determining the gas permeability. The permeability of the systems was correlated with blend morphology and dispersion of the nanoclay platelets in the polymer blend.

The fabrication of superadsorbent for dye adsorption is a hot research area at present. However, the development of low-cost and highly efficient superadsorbents against toxic textile dyes is still a big challenge. Here, we fabricated hydrophobic cellulose nanofiber aerogels from cellulose nanofibers through an eco-friendly silanization reaction in liquid phase, which is an extremely efficient, rapid, cheap, and environmentally friendly procedure. Moreover, the demonstrated eco-friendly silanization technique is easy to commercialize at the industrial level. Most of the works that have reported on the hydrophobic cellulose nanofiber aerogels explored their use for the elimination of oil from water. The key novelty of the present work is that the demonstrated hydrophobic cellulose nanofibers aerogels could serve as superadsorbents against toxic textile dyes such as crystal violet dye from water and insulating materials for building applications. Here, we make use of the possible hydrophobic interactions between silane-modified cellulose nanofiber aerogel and crystal violet dye for the removal of the crystal violet dye from water. With a 10 mg/L of crystal violet (CV) aqueous solution, the silane-modified cellulose nanofiber aerogel showed a high adsorption capacity value of 150 mg/g of the aerogel. The reason for this adsorption value was due to the short-range hydrophobic interaction between the silane-modified cellulose nanofiber aerogel and the hydrophobic domains in crystal violet dye molecules. Additionally, the fabricated silane-modified cellulose nanofiber hydrophobic aerogels exhibited a lower thermal conductivity value of 0.037 W·m -1 K -1 , which was comparable to and lower than the commercial insulators such as mineral wools (0.040 W·m -1 K -1 ) and polystyrene foams (0.035 W·m -1 K -1 ). We firmly believe that the demonstrated silane-modified cellulose nanofiber aerogel could yield an eco-friendly adsorbent that is agreeable to adsorbing toxic crystal violet dyes from water as well as active building thermal insulators.

Phenolic antioxidants such as tert-butylhydroquinone (TBHQ) can prolong the shelf life of edible oils by delaying the oxidation process. The excessive use of TBHQ can damage food quality and public health, so it is necessary to develop an efficient TBHQ detection technique. In this work, nickel-aluminum double hydroxide (NiAl-LDH) was grown on glucose carbon spheres (GC), which formed porous carbon nanomaterials (named NiAl-LDH@GC-800) after pyrolysis at 800 °C. The successful synthesis of the material was verified by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The obtained NiAl-LDH@GC-800 was dopped onto a glass carbon electrode to prepare an electrochemical sensor for TBHQ. The synergistic effect of porous carbon and Ni metal reduced from NiAl-LDH by high-temperature calcination accelerated the electron transfer rate and improved the sensitivity of the sensor. The prepared sensor showed a low limit of detection (LOD) of 8.2 nM, a high sensitivity (4.2 A·M−1), and a good linear range (20~300 µM) in detecting TBHQ. The sensor was also successfully used for TBHQ detection in edible oils, including chili oil, peanut oil, and rapeseed oil. [ABSTRACT FROM AUTHOR]

The effect of potassium impregnation at different concentrations during gasification, under nitrogen/water steam atmosphere, of char produced via pyrolysis of olive mill residues blended or not with pine sawdust was investigated. Three concentrations (0.1 M, 0.5 M, and 1.5 M) of potassium carbonate solution (K2CO3) were selected to impregnate samples. First, four types of pellets were prepared; one using exhausted olive mill solid waste (G) noted (100G) and three using G blended with pine sawdust (S) in different percentages (50%S–50%G (50S50G); 60%S–40%G (60S40G); 80%S–20%G (80S20G)). Investigations showed that when isothermal temperature increases during the gasification conducted with two water steam percentages of 10% and 30%, the reactivity increases with potassium concentration up to 0.5 M, especially for 100G. Still, higher catalyst concentration (1.5 M) showed adverse effects attributable to silicon release and char pore fouling. Moreover, the effect of the steam concentration on the gasification reactivity was significant with the non-impregnated sample 100G. Finally, a kinetic study was carried out to determine the different kinetic parameters corresponding to the Arrhenius law. [ABSTRACT FROM AUTHOR]

Despite extensive studies of deposited carbon in Fischer–Tropsch synthesis (FTS), an atomic-level comprehension of the effect of carbon on the morphology of cobalt-based FTS catalysts remains elusive. The adsorption configurations of carbon atoms on different crystal facets of hexagonal close-packed (hcp) Co nanoparticles were studied using density functional theory (DFT) calculations to explore the interaction mechanism between C and Co surfaces. The weaker adsorption strength of C atoms on Co(0001), Co(10-10), and Co(11-20) surfaces accounted for lower diffusion energy, leading to the facile formation of C dimers. Electronic property analysis shows that more electrons are transferred from Co surfaces to C atoms on corrugated facets than on flat facets. The deposition of carbon atoms on Co nanoparticles affects surface energy by forming strong Co-C bonds, which causes the system to reach a more energetically favorable morphology with an increased proportion of exposed Co(10-12) and Co(11-20) areas as the carbon content increases slightly. This transformation in morphology implies that C deposition plays a crucial role in determining the facet proportion and stability of exposed Co surfaces, contributing to the optimization of cobalt-based catalysts with improved performance. [ABSTRACT FROM AUTHOR]

Currently, one of the topical directions in the field of production and application of graphene-like nanostructures is the use of renewable natural raw materials, which have unlimited resources for an economically efficient large-scale yield of a product with environmental safety. In this regard, we present the production of graphene oxide (GO) from a renewable natural raw material of plant biomass, birch activated carbon (BAC), and a comparison of the obtained physicochemical, mechanical, and electrical properties of birch activated carbon–graphene oxide (BAC–GO) and graphite–graphene oxide (G–GO) synthesized from the initial materials, BAC and graphite (G). Results obtained from this study confirm the successful oxidation of BAC, which correlates well with the physical–chemical dates of the G–GO and BAC–GO samples. Change in data after the oxidation of graphite and BAC was facilitated by the structure of the starting materials and, presumably, the location and content of functional oxygen-containing groups in the G–GO and BAC–GO chains. Based on the results, the application of a cost-effective, eco-friendly colloidal solution of nanodispersed BAC–GO from a plant biomass-based high-quality resource for producing large-scale nanostructured graphene is validated which has potential applicability in nanoelectronics, medicine, and other fields. [ABSTRACT FROM AUTHOR]

Polyvinyl chloride (PVC) resins are widely used in modern society due to their acid and alkali resistance, low cost, and strong insulation properties. However, the high chlorine (Cl) content in PVC poses significant challenges for its recycling. This study reviews the treatment processes, model construction, and economic and environmental assessments to construct a methodological framework for the sustainable development of emerging dechlorination technologies. In terms of treatment processes, this study summarizes three types of processes, pretreatment, simultaneous dechlorination during chemical recycling, product purification, and emphasizes the necessity of dechlorination treatment from a systematic perspective. Additionally, the construction of models for dechlorination processes is investigated from the laboratory to the industrial production system to macro-scale material, in order to evaluate the potential inventory data and material metabolism behaviors. This review also summarized the methodology framework of Techno-Economic Analysis (TEA) and Life Cycle Assessment (LCA), which can be applied for evaluation of the economic and environmental performance of the dechlorination processes. Overall, this review provides readers with a comprehensive perspective on the state-of-the-art for PVC dechlorination technologies, meanwhile offering sustainable guidance for future research and industrial applications of chemical recycling of PVC waste. [ABSTRACT FROM AUTHOR]

Calcium phosphates (CaPs) and their substituted derivatives encompass a large number of compounds with a vast presence in nature that have aroused a great interest for decades. In particular, hydroxyapatite (HAp, Ca10(OH)2(PO4)6) is the most abundant CaP mineral and is significant in the biological world, at least in part due to being a major compound in bones and teeth. HAp exhibits excellent properties, such as safety, stability, hardness, biocompatibility, and osteoconductivity, among others. Even some of its drawbacks, such as its fragility, can be redirected thanks to another essential feature: its great versatility. This is based on the compound's tendency to undergo substitutions of its constituent ions and to incorporate or anchor new molecules on its surface and pores. Thus, its affinity for biomolecules makes it an optimal compound for multiple applications, mainly, but not only, in biological and biomedical fields. The present review provides a chemical and structural context to explain the affinity of HAp for biomolecules such as proteins and nucleic acids to generate hybrid materials. A size-dependent criterium of increasing complexity is applied, ranging from amino acids/nucleobases to the corresponding macromolecules. The incorporation of metal ions or metal complexes into these functionalized compounds is also discussed. [ABSTRACT FROM AUTHOR]

This review examines the potential of municipal solid waste (MSW) as a renewable energy source, focusing on recent advances in thermochemical conversion technologies and their environmental impacts. The exponential growth of urban populations has led to a surge in MSW, necessitating sustainable waste management solutions. Traditional disposal methods, such as landfilling and incineration, have significant environmental drawbacks. However, advancements in waste-to-energy (WtE) technologies, including incineration, pyrolysis, and gasification, offer promising alternatives for energy recovery and resource utilization. This review explores the composition of MSW, its classification as a renewable resource, and the thermochemical conversion technologies that transform waste into energy. The environmental impacts of these technologies, particularly emissions and air quality concerns, are critically analyzed. The review highlights the evolving regulatory landscape and the implementation of advanced emission reduction systems. The findings underscore the importance of integrating innovative waste management strategies to promote a circular economy and achieve sustainable development goals. [ABSTRACT FROM AUTHOR]

Microplastics are contaminants in marine ecosystems, posing great threats to biota and human health. In this work, we provide an overview of the progress made in understanding microplastic prevalence in tropical coastal environments, focusing on the Johor and the Singapore Straits as a case study. We examine the sources, distribution, transport, and ecological impact of microplastic pollution in this region through a systematic review. All papers relating to marine microplastics in Singapore's sand and benthic sediments, seawater, and marine biota were used for analysis, from 2004 to 2023. In addition, we discuss the influence of envi-ronmental factors such as coastal morphology and anthropogenic activities on patterns of microplastic accumulation. We emphasize that microplastic pollution is more prevalent along the eutrophic Johor Strait compared to the Singapore Strait due to hydrological conditions. Rainfall is also a key factor that influences mi-croplastic abundance during the monsoon seasons. Furthermore, the bacterial and plankton assemblages of organisms on microplastic surfaces are diverse, with eutrophic waters enhancing the diversity of organisms on microplastic surfaces. Novel harmful cyanobacteria and bloom species of phytoplankton were also found on microplastic surfaces. By synthesizing existing research findings and highlighting regional characteristics, this paper contributes to ongoing efforts to mitigate microplastic pollution in tropical regions. [ABSTRACT FROM AUTHOR]

Municipal solid waste management has become a critical global issue due to the rapid increase in waste generation driven by urbanization and population growth. This surge in waste poses significant environmental, social, and health challenges, exacerbated by inefficient recycling and waste-to-energy facilities. Effective waste management requires comprehensive strategies encompassing waste reduction, efficient collection, sorting systems, and advanced recycling and energy recovery technologies. This study highlights the potential of incineration as a waste-to-energy solution, specifically focusing on Kuwait. By analyzing various waste management technologies and their applicability, this study emphasizes the role of incineration in transforming municipal solid waste into electricity, thereby reducing landfill use and environmental impacts. The research includes a detailed review of the existing technologies, a case study on Kuwait's waste management practices, and an evaluation of the economic and environmental benefits of implementing waste-to-energy incineration. The findings underscore the importance of tailored waste management solutions to address specific regional challenges, promote sustainability, and enhance public health and well-being. [ABSTRACT FROM AUTHOR]

The management of drinking water treatment plant (DWTP) sludge is challenging for water treatment facilities. Previous studies reported mainly on handling sludge through landfilling, release into water bodies, discharge into wastewater treatment plants, onsite disposal, and incineration methods for the treatment of sludge. The limitations of these sludge-handling methods are well documented. This article focuses on the hierarchical approach as an alternative and comprehensive method for handling DWTP sludge. The core of hierarchical management streamlines the minimization of the generated DWTP sludge; treatment of DWTP sludge to reduce toxicity; changing of the physicochemical form of DWTP sludge; and finally, the reuse, recycling, and recovery of DWTP sludge. The premise is to achieve zero landfilling of DWTP sludge, establish a circular economy, generate job opportunities, and preserve the environment. Thus, this study also proposes two main technologies, which are gravity-based sludge separators for fractionating the sludge and photocatalytic membrane reactors (PMRs) as a technology for the treating and/or recovery of nutrients and minerals from DWTP sludge. Until the chemical deductive or minus approach becomes a reality in water treatment, the use of PMRs and gravity-based sludge separators will enhance the management of DWTP sludge when incorporated into the hierarchical approach. [ABSTRACT FROM AUTHOR]

In this study, a decentralized incineration facility was evaluated over a three-year period, focusing on performance aspects, such as the burning rate, ash production, fuel and electricity consumption, and ash composition, while processing animal by-products (ABPs). The total cost for ABP incineration was determined to be EUR 159 t−1 ABP, with the major components being capital depreciation (42%), maintenance expenditures (26%), labor (18%), and transportation costs (9%). Liquified petroleum gas consumption ranged from 3 to 7 kg t−1, while electricity use was between 15 and 20 kWh t−1 incinerated ABP. The incineration process generated 7–10% (by weight) ABP ash, which was characterized by high calcium and phosphorus contents and low levels of hazardous trace elements. Leaching tests demonstrated the potential for recovering an alkaline supernatant for flue gas treatment and a phosphorus-rich slurry for fertilizer production. The findings suggest that energy recovery and valorization are crucial for minimizing the operational costs and the environmental impact, emphasizing the benefits of integrating advanced resource recovery techniques in ABP incineration facilities. [ABSTRACT FROM AUTHOR]

The Brazilian Policy foresees the waste management hierarchy, according to which energy reuse from waste is preferred to final disposal. However, less than 0.2% of the country's waste goes to energy production. This paper proposes sustainability indicators to support the decision to choose the best process to treat municipal solid waste (MSW) through bioenergy generation technologies. Then, we conduct a case study for Rio de Janeiro. Incineration and gasification were not economically feasible—despite TRL 9 and 8. However, the projects presented a null net present value by increasing the gate fee to 94.69 and 255.39 USD/ton of MSW, respectively. The social indicators (job creation, salary increase with the absorption of waste pickers, population served, reduction in MSW sent to landfill) did not indicate the best technology. The results of the environmental indicators for incineration and gasification were, respectively, 0.45 and 0.37 t CO2eq/tMSW for GWP, 1.49 and 1.23 MWh/tMSW for energy intensity, 1.24 and 6.14 m3/tMSW for water intensity, 39.3 and 27.9 m2/tMSW for land use and 0.135 and 0.088 t SO2eq/tMSW for acidification. Gasification presented better results on 60% of the environmental indicators. However, incineration scored better in the important ones, water and energy intensities, in addition to the technical–economic aspect. [ABSTRACT FROM AUTHOR]

Commercial silica support pellets were impregnated and calcined to contain cobalt oxide and ruthenium oxide for Fischer-Tropsch synthesis (FTS). The precatalyst pellets were split evenly into two groups, the control precatalyst (c-precat) and silylated precatalyst (s-precat), which were treated with 1H,1H, 2H, 2H-perfluorooctyltriethoxysilane (PFOS) in toluene. The samples of powderized s-precat were superhydrophobic, as determined by the water droplet contact angle (>150°) and sliding angle (<1°). Thermal analysis revealed the PFOS groups to be thermally stable up to 400 °C and temperature programmed reduction (TPR) studies showed that H2 reduction of the cobalt oxide to cobalt was enhanced at lower temperatures relative to the untreated c-precat. The two active catalysts were examined for their FTS performance in a tubular fixed-bed reactor after in situ reduction at 400 °C for 16 h in flowing H2 to give the active catalysts c-cat and s-cat. The FTS runs were performed under identical conditions (255 °C, 2.1 MPa, H2/CO = 2.0, gas hourly space velocity (GHSV) 510 h–1) for 5 days. Each catalyst was examined in three runs (n = 3) and the mean values with error data are reported. S-cat showed a higher selectivity for C5+ products (64 vs. 54%) and lower selectivity for CH4 (11 vs. 17%), CO2 (2 % vs. 4 %), and olefins (8% vs. 15%) than c-cat. S-cat also showed higher CO conversion, at 37% compared to 26%, leading to a 64% increase in the C5+ productivity measured as g C5+ products per g catalyst per hour. An analysis of the temperature differential between the catalyst bed and external furnace temperature showed that s-cat was substantially more active (DTinitial = 29 °C) and stable over the 5-day run (DTfinal = 22 °C), whereas the attenuated activity of c-cat (DTinitial = 16 °C) decayed steadily over 3 days until it was barely active (DTfinal < 5 °C). A post-run surface analysis of s-cat revealed no change in the water contact angle or sliding angle, indicating that the FTS operation did not degrade the PFOS surface treatment. [ABSTRACT FROM AUTHOR]

The real implementation of biogas reforming at an industrial scale to obtain interesting products (like hydrogen or syngas) is a developing research field where multidisciplinary teams are continuously adding improvements and innovative technologies. These works can contribute to the proliferation of green technologies where the circular economy and sustainability are key points. To assess the sustainability of these processes, there are different tools like life cycle assessment (LCA), which involves a complete procedure where even small details count to consider a certain technology sustainable or not. The aim of this work was to review works where LCA is applied to different aspects of biogas reforming, focusing on the role of catalysts, which are essential to improve the efficiency of a certain process but can also contribute to its environmental impact. In conclusion, catalysts have an influence on LCA through the improvement of catalytic performance and the impact of their production, whereas other aspects related to biogas or methane reforming could equally affect their catalytic durability or reusability, with a subsequent effect on LCA. Further research about this subject is required, as this is a continuously changing technology with plenty of possibilities, in order to homogenize this research field. [ABSTRACT FROM AUTHOR]

Waste valorization is necessary in today's society to achieve a sustainable economy and prosperity. In this work, a novel approach to the waste valorization of cuttlebone was investigated. This material was ground and calcined at 900 °C for 5 h in an inert atmosphere. The resulting calcined cuttlebone (CCB) was characterized using XRD, SEM, FTIR, BET, TGA, Zetasizer, and potential methods. The main phases in the CCB were determined to be CaO, MgO, Ca3(PO4)2, and residual carbon. CCB was investigated as an adsorbent for the removal of dye from simulated wastewater streams. The maximum adsorption capacities for rhodamine B and crystal violet dyes were estimated to be 519 and 921 mg/g, respectively. For both dyes, the Avrami model was the best-fit model for representing adsorption kinetics. The study of adsorbent regeneration for CV as a representative example involved the use of several chemical solvents. Ethanol solvent was shown to have the highest adsorbent regeneration method efficiency, reaching 65.20%. In addition, CCB was investigated for methanol electro-oxidation for energy generation. As the methanol concentration increased, the maximum current density produced by the CCB increased, reaching approximately 50 mA/cm2. This work paves the way toward waste valorization of natural matter for sustainable production and consumption of material, as per the requirements of the circular economy principles. [ABSTRACT FROM AUTHOR]

This paper examines the application of non-synthetic particle suspensions as a support medium for the additive manufacturing of complex doubly curved ceramic shells with overhangs between 0° and 90° using clay paste. In this method, the build-up material is injected within a constant volume of air-permeable particle suspension. As the used clay paste does not solidify right after injection, the suspension operates like a support medium and enables various print path strategies. Different non-synthetic suspension mixtures, including solid and flexible components such as quartz sand, refractory clay, various types of wood shavings, and cotton flocks, were evaluated for their ability to securely hold the injected material while allowing drying of the water-based clay body and its shrinkage. The balance between grain composition, added water, and the compressibility of the mixture during printing and drying played a pivotal role in the particle suspension design and assessment. Furthermore, the moisture absorption of the particle suspension and the structural integrity of the layer bond of the fired ceramics were also assessed. The examined additive manufacturing process not only enables the production of meso-scale doubly curved ceramic shells with average overhang of 56° but also introduces a new practice for designing specialized surfaces and constructions. [ABSTRACT FROM AUTHOR]

The consistent rise of the per capita waste generation rate has led to an escalation of waste quantities and the need to expand waste disposal methods. Efforts to develop clean and affordable energy systems are increasingly linked to waste-to-energy as part of the transition to a circular economy (CE). A resource-efficient waste-to-energy business model within a CE offers a variety of environmentally friendly waste management options based on their overall environmental impacts but also makes efficient use of available resources and technologies to convert different types of waste into energy, which helps reduce the adverse effects on the environment and create additional energy sources. This research aims to identify innovative waste management solutions to foster the implementation of CE and a more resource-efficient business model. The research methodology is based on qualitative and quantitative research, triangulation, material flow assessment, and systems dynamics. The value of this study is within the analysis of existing waste-to-energy plant case studies to identify a set of recommendations and appropriate business models for the countries that are at an early stage of evaluation of such facilities. This study found that waste-to-energy plants are critical to achieving the EU's waste disposal targets by 2035. The findings highlight the importance of supporting mechanisms in the waste sector, such as structural funds, as the industry primarily focuses on societal health and safety and environmental protection, alongside resource efficiency and circularity potential. [ABSTRACT FROM AUTHOR]

A significant waste material threatening sustainability efforts are post-consumer food packaging goods. These ubiquitous multi-materials comprise chemically disparate components and are thus challenging targets for recycling. Herein, we undertake a proof-of-principle study in which we use a single-stage method to convert post-consumer multi-material food packaging (post-consumer peanut butter jars) to a high compressive strength composite (PBJS90). This is accomplished by thiocracking the ground jar pulp (10 wt. %) with elemental sulfur (90 wt. %) at 320 °C for 2 h. This is the first application of thiocracking to such mixed-material post-consumer goods. Composite synthesis proceeded with 100% atom economy, a low E factor of 0.02, and negative global warming potential of −0.099 kg CO2e/kg. Furthermore, the compressive strength of PBJS90 (37.7 MPa) is over twice that required for Portland cement building foundations. The simplicity of composite synthesis using a lower temperature/shorter heating time than needed for mineral cements, and exclusive use of waste materials as precursors are ecologically beneficial and represent an important proof-of-principle approach to using thiocracking as a strategy for upcycling multi-materials to useful composites. [ABSTRACT FROM AUTHOR]

Dry reforming of methane (DRM) is considered one of the most promising technologies for efficient greenhouse gas management thanks to the fact that through this reaction, it is possible to reduce CO2 and CH4 to obtain syngas, a mixture of H2 and CO, with a suitable ratio for the Fischer–Tropsch production of long-chain hydrocarbons. Two other main processes can yield H2 from CH4, i.e., Steam Reforming of Methane (SRM) and Partial Oxidation of Methane (POM), even though, not having CO2 as a reagent, they are considered less green. Recently, scientists' challenge is to overcome the many drawbacks of DRM reactions, i.e., the use of precious metal-based catalysts, the high temperatures of the process, metal particle sintering and carbon deposition on the catalysts' surfaces. To overcome these issues, one proposed solution is to implement photo-thermal dry reforming of methane in which irradiation with light is used in combination with heating to improve the efficiency of the process. In this paper, we review the work of several groups aiming to investigate the pivotal promoting role of light radiation in DRM. Focus is also placed on the catalysts' design and the progress needed for bringing DRM to an industrial scale. [ABSTRACT FROM AUTHOR]

Biomass waste, which is biodegradable and vastly underutilized, is generated in huge quantities worldwide. Forestry and agricultural biomass wastes are notable for their wide availability, high yield, biodegradability, and recyclability. The accumulation of these wastes not only occupies valuable land but causes serious environmental pollution, which can ultimately harm human health. Therefore, leveraging scientific technology to convert forestry and agricultural bio-waste into bioenergy and other valuable products is crucial. In this paper, common forestry and agricultural bio-waste such as straw, rice husks, livestock manure, tree branches, sawdust, and bioenergy (bioethanol, biogas, biodiesel, biohydrogen) were selected as keywords, with the theme of green and efficient utilization. This paper provides a comprehensive review of the sources of biomass waste, existing recycling technologies, and the potential of forestry and agricultural bio-waste as material additives and for conversion to biomass energy and other derivatives, along with future recycling prospects. [ABSTRACT FROM AUTHOR]

This study aims to provide an overview of the growing need for renewable energy conversion and aligns with the broader context of environmentally friendly energy, specifically through producing syngas from biomass. Unlike natural gas, which is mainly composed of methane, syngas contains a mixture of combustible CO, H2, and CnHm. Therefore, optimizing its production requires a thorough examination of various operational parameters such as the gasifying agent, the equivalence ratio, the biofuel type, and the state, particularly in densified forms like pellets or briquettes. As new biomass sources are continually discovered and tested, operational parameters are also constantly evaluated, and new techniques are continuously developed. Indeed, these techniques include different gasifier types and the use or non-use of catalysts during biofuel conversion. The present study focuses on these critical aspects to examine their effect on the efficiency of syngas production. It is worth mentioning that syngas is the primary gaseous product from gasification. Moreover, it is essential to note that the pyrolysis process (prior to gasification) can produce, in addition to tar and char, a mixture of gases. The common feature among these gases is their versatility in energy generation, heat production, and chemical synthesis. The analysis encompasses the resulting gas features, including the yield and composition, mainly through the hydrogen-to-carbon monoxide ratio and the carbon monoxide-to-carbon dioxide ratio, as well as the lower heating value and considerations of the tar yield. [ABSTRACT FROM AUTHOR]

Solid particles as heat absorptances and storage mediums promise enhanced energy storage densities in concentrated solar power/thermal (CSP/T) plants. Employment of metallurgical slags as a secondary precursor material for solid particle preparation is ecologically and economically beneficial. Although these processed wastes, comprised of several oxides, exhibit generally promising high-temperature properties, chemical scattering from batch to batch may result in distinct material and functional properties, which may be an obstacle for their utilization. In this study, a steelmaking slag, LiDonit (LD), produced using a unique controlled slag treatment with high reproducibility is investigated as a candidate material. The aforementioned subsequent unique slag treatment makes LD a very promising and distinguishable secondary raw material for high-temperature applications. The as-received microstructure, phase components, and chemical composition of the LD material were analyzed to understand its material properties and to assess its reproducibility. The as-received LD chunks were transferred into pellets by subsequent milling, gel-casting, and sintering stages to reveal the potential processing routes. The CSP/T-related properties of sintered pellets, such as high temperature stability, heat capacity, and solar absorptance, were also examined to reveal their potential use in CSP/T applications and expand application areas with high added value. [ABSTRACT FROM AUTHOR]

In this study, calcium-rich resource minerals such as brushite, tricalcium phosphate (TCP), and hydroxyapatite were tested as catalysts for the methanolysis of alkaline solutions of NaBH4 to generate hydrogen H2. The synthesis of calcium phosphate compounds was characterized by means of X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The hydrogen generation rate with the TCP catalyst (15,214 mL min−1 g−1) was higher than with the hydroxyapatite catalyst (12,437 mL min−1 g−1) and brushite catalyst (6210 mL min−1 g−1) for the methanolysis of 250 mg NaBH4 at 298 K using 25 mg of catalyst. The impact of TCP weight on hydrogen generation was studied. The methanolysis reaction led to a higher hydrogen volume generation over time with an increase in the weight of the TCP catalyst at a temperature of 308 K. The calculated activation energy for NaBH4 hydrolysis with the TCP catalyst was 23.944 kJ mol−1, suggesting the high catalytic activity of TCP. The values of enthalpy (ΔH) and entropy (ΔS) were calculated, and the results showed that ΔH was 21.28 kJ mol−1 and ΔS was −93.096 J·mol−1. ΔH was positive, meaning that the reaction was endothermic, and the negative ΔS meant a decrease in the disorder of the methanolysis reaction. The stability of the catalysis was tested in successive methanolysis tests. The catalyst's efficiency decreased to 89% after four cycles. [ABSTRACT FROM AUTHOR]

Commercial non-functionalized (CNTs) and functionalized carbon nanotubes (CNT-COOH and CNT-NH2) were used as supports to synthesize vanadium-supported catalysts to be used in the gas phase partial oxidation of furfural towards maleic anhydride (MA). The CNTs and the VO2-V2O5/CNTs, so-called VO/CNT catalysts, were characterized by AAS, TGA, XRD, N2 adsorption isotherms at −196 °C, Raman, NH3-TPD and XPS. The surface area values, TGA and XRD results indicate that the larger thermal stability and larger dispersion of vanadium species is reached for the VO/CNT-NH2 catalyst. XPS indicates presence of surface VO2 and V2O5 species for the non-functionalized (CNT) and functionalized (CNT-COOH and CNT-NH2) catalysts, with a large interaction of the functional group with the surface vanadium species only for the VO/CNT-NH2 catalyst. The catalytic activity, evaluated in the range 305 °C to 350 °C, indicates that CO, CO2 and MA yield (%) and MA productivity are associated to the redox properties of the vanadium species, the oxygen exchange ability of the support and the vanadium–support interaction. For the reaction temperatures between 320 °C and 335 °C, the maximum MA yield (%) is found in the functionalized VO/CNT-COOH and VO/CNT-NH2 catalysts. This behavior is attributed to a decreased oxidation capability of the CNT with the functionalization. In addition, VO/CNT-NH2 is the more active and selective catalyst for MA productivity at 305 °C and 320 °C, which is related to the greater interaction of the surface vanadium species with the -NH2 group, which enhances the redox properties and stabilization of the VO2 and V2O5 surface active sites. Recycling at 350 °C resulted in 100% furfural conversion for all catalysts and a similar MA yield (%) compared to the fresh catalyst, indicating no loss of surface active sites. [ABSTRACT FROM AUTHOR]

Cobalt carbides have been recognized as an active phase for the production of light olefins and alcohols in Fischer–Tropsch synthesis. In this study, in situ X-ray diffraction experiments were performed to investigate the stability and catalytic performance over a single-phase Co3C catalyst under reaction conditions. The in situ X-ray diffraction results indicated that the Co3C phase remained stable with no significant changes until the temperature reached 300 °C. The high stability can be attributed to the twinning structure of the single-phase Co3C catalyst. The catalytic evaluation results showed that the single-phase Co3C catalyst had higher activity with high selectivity to long-chain products due to the unique surface structure of Co3C. This work provides guidance for the rational design of efficient cobalt carbide catalysts for Fischer–Tropsch synthesis reactions. [ABSTRACT FROM AUTHOR]

Plastics are predominant in numerous sectors like packaging, agriculture, hardware, electronics, and many others. Annual plastic demand has been rapidly growing in the last few decades because of the increasing dependency on plastics. As a consequence, massive amounts of plastic waste are being generated every year. These plastic wastes are non-biodegradable, and hence their disposal poses a serious threat to the ecosystem and causes significant environmental problems such as endangering the safety of marine life, wildlife, air, water, and soil, etc. A large portion of plastic waste ends up in landfills, and only a small fraction is recycled. The continuous dependence on landfills as the main disposal method for plastic waste is costly and ineffective. Common solutions to plastic waste management are incineration and recycling; however, incineration emits harmful pollutants and greenhouse gases that contribute to ozone layer depletion and global warming; moreover, recycling is expensive and inefficient. As an alternative to recycling and incineration, the pyrolysis process can convert plastic wastes into more valuable fuel products. Pyrolysis is a thermal process that converts raw material into pyrolysis liquid, solid wax, and non-condensable gases in the absence of oxygen. This process is attractive because it is economical and energy-efficient, and it can be used to convert various types of plastic waste into valuable products. In recent years, there have been significant developments in pyrolysis applications in liquid fuel production from plastic wastes. This work reviews recent advances in and challenges for the pyrolysis process for converting plastic wastes into a valuable alternative fuel, focusing on studies of advanced pyrolysis processes published over the last five years. The paper also highlights the numerical modeling of pyrolysis of plastic wastes and the potential impact of pyrolysis on the future of sustainable waste-management practices of plastics. [ABSTRACT FROM AUTHOR]

To investigate the control mechanisms of NOx precursors and the synergistic effects of composite catalysts during proline pyrolysis, a systematic series of experiments was conducted utilizing composite catalysts with varying Fe-Ca ratios. Product distribution analysis was employed to elucidate the catalysts' mechanisms in reducing NOx precursor emissions. The synergistic interactions between Fe and Ca were quantitatively assessed through comparative theoretical and experimental release calculations. The results indicate that an increase in the Fe content in the catalyst led to a rise in amine concentrations from 0.9% to 2.95%, implying that Fe facilitates the generation of amine-N through ring-opening and substitution reactions. When the Fe to Ca ratio was balanced at 1:1, nitrogen predominantly participated in the formation of purines via cyclization and substitution reactions. Additionally, all composite catalysts exhibited a suppressive effect on the release of NOx precursors, attributed to their significant enhancement of solid product retention. Fe-Ca composite catalyst synergistically inhibits the release of gaseous nitrogen. Notably, the strongest synergistic effect was observed with a 1:3 Fe to Ca ratio, which reduced the release of NH3 by 38.7% and HCN by 53.6% during proline pyrolysis. This study offers valuable insights into the control of NOx precursors and the optimization of nitrogen-rich biomass pyrolysis processes. [ABSTRACT FROM AUTHOR]

Carbonated apatite (CAp), known as the main mineral that makes up human bone, can be utilized in conjunction with scaffolds to increase their bioactivity. Various methods (e.g., co-precipitation, hydrothermal, and biomimetic coatings) have been used to provide bioactivity by forming CAp on surfaces similar to bone minerals. Among them, the use of simulated body fluids (SBF) is the most popular biomimetic method for generating CAp, as it can provide a mimetic environment. However, coating methods using SBF require at least a week for CAp formation. The long time it takes to coat biomimetic scaffolds is a point of improvement in a field that requires rapid regeneration. Here, we report a step-wise biomimetic coating method to form CAp using calcium carbonate vaterite (CCV) as a precursor. We can manufacture CCV-transformed CAp (V-CAp) on the surface in 4 h at least by immersing CCV in a phosphate solution. The V-CAp deposited surface was analyzed using scanning electron microscopy (SEM) images according to the type of phosphate solutions to optimize the reaction conditions. X-ray diffraction (XRD) and attenuated total reflection-Fourier transform infrared (ATR-FTIR) analysis validated the conversion of CCV to V-CAp on surfaces. In addition, the bioactivity of V-CAp coating was analyzed by the proliferation and differentiation of osteoblasts in vitro. V-CAp showed 2.3-folded higher cell proliferation and 1.4-fold higher ALP activity than the glass surface. The step-wise method of CCV-transformed CAp is a biocompatible method that allows the environment of bone regeneration and has the potential to confer bioactivity to biomaterial surfaces, such as imparting bioactivity to non-bioactive metal or scaffold surfaces within one day. It can rapidly form carbonated apatite, which can greatly improve time efficiency in research and industrial applications. [ABSTRACT FROM AUTHOR]

Waste incineration with energy recovery is a matured Waste-to-Energy (WtE) technology which has contributed immensely to the disposal and management of Municipal Solid Waste (MSW) in industrialised nations. The adoption of this technology in developing countries is currently gaining momentum due to the numerous benefits that can be derived from its use. In this study, a techno-economic assessment of MSW incineration in proposed waste incineration facilities for use in Ghana was carried out. The technical assessment was conducted by determining the plant capacity and annual electricity production based on the combustible residues of MSW collected from various population sizes in the country, while the economic assessment was carried out by determining two key economic indicators, Net Present Value (NPV) and Levelised Cost of Energy (LCOE). It was found that a total of about 400 MW of electricity can be generated from the total of about 14,000 tonnes of MSW generated in the country daily. The NPV for a 35.81 MW installed capacity of waste incineration facility was found to be USD 166,410,969.24. However, the LCOE for the 35.81 MW capacity and all others considered was greater than the tariff of electricity for their respective capacities, which means waste incineration facilities are not economically viable ventures in Ghana. The implementation of these facilities in the country would, therefore, need governmental support in the form of subsidies and tax rebates. Three locations were proposed for the piloting of waste incineration facilities in the country, and these locations are in the Accra Metropolitan, Asokore-Mampong Metropolitan, and Sekondi-Takoradi Metropolitan Assemblies. [ABSTRACT FROM AUTHOR]

In the current study, the synthesis of hydroxyapatite-ceria (HAP-CeO2) scaffolds is attempted through a bioinspired chemical approach. The utilized colloidal CeO2 suspension presents antifungal activity against the Aspergillus flavus and Aspergillus fumigatus species at concentrations higher than 86.1 ppm. Three different series of the composite HAP-CeO2 suspensions are produced, which are differentiated based on the precursor suspension to which the CeO2 suspension is added and by whether this addition takes place before or after the formation of the hydroxyapatite phase. Each of the series consists of three suspensions, in which the pure ceria weight reaches 4, 5, and 10% (by mass) of the produced hydroxyapatite, respectively. The characterization showed that the 2S series's specimens present the greater alteration towards their viscoelastic properties. Furthermore, the 2S series's sample with 4% CeO2 presents the best mechanical response. This is due to the growth of needle-like HAP crystals during lyophilization, which—when oriented perpendicular to the direction of stress application—enhance the resistance of the sample to deformation. The 2S series's scaffolds had an average pore size equal to 100 μm and minimum open porosity 89.5% while simultaneously presented the lowest dissolution rate in phosphate buffered saline. [ABSTRACT FROM AUTHOR]

Water treatment sludge (WTS) is the residue produced during water treatment processes for public use. Exploring the reintroduction of these wastes into the production chain to generate new, value-added materials presents a current challenge. This could promote their reuse and reduce the negative environmental impacts associated with their disposal. This study assessed the technical feasibility of using aluminum-based WTS to partially replace silty sand soil in mixtures that include two stabilizers (hydrated lime and Portland cement), potentially for use in road pavements. After conducting a thorough physical, chemical, and geotechnical characterization of both the soil and the sludge, bench-scale experiments were carried out to test the mixtures' resistance, with WTS proportions of 5%, 8%, 10%, 15%, and 20%, stabilized with either lime or cement. The findings confirm that WTS does not contain potentially toxic elements, according to Brazilian standards, and all tested composites appear suitable for paving. However, the mechanical resistance of the soil–sludge–cement mixtures decreases as the WTS content increases, with an optimum California bearing ratio (CBR) of 41.50% achieved at a 5% WTS addition. Meanwhile, incorporating 15% WTS into soil–sludge–lime mixtures resulted in the highest CBR value of 21.25% for this type of mixture. It is concluded that incorporating stabilizers into soil–WTPS mixtures for road construction allows for an increased percentage of WTPS in silty-sandy soils. Further studies are recommended with different soil types and the addition of fibers to the mixes, to assess the long-term performance of the structure, along with economic and environmental analyses. [ABSTRACT FROM AUTHOR]

In this work, gold-photo-catalyzed CO2 transformation was conducted and the effect of three variables with two levels was investigated: support (TiO2 and hydroxyapatite from bovine bone (BB)), Au content (5 and 10%) and activation wavelength (254 and 380–700 nm). Reactions were conducted in a stirred tank reactor by bubbling CO2 (9 × 10−3 dm3/min) in 0.1 dm3 of 0.5 M NaOH solution. The catalysts were synthesized using AuCl3, TiO2 and BB. Au nanoparticles were obtained by reduction with Hetheroteca inuloides, thus eliminating calcination and hydrogenation to reduce the gold species. By TEM, the particle size distribution was determined, and the synthesized nanoparticle sizes varied in the range of 9 to 19 nm, depending on the support and Au content. By UV–Vis spectroscopy, the energy band gaps of the prepared materials were 2.18 eV (10% Au/BB), 2.38 eV (5% Au/BB), 2.42 eV (BB), 3.39 eV (5% Au/TiO2), 3.41 eV (10% Au/TiO2) and 3.43 eV for pure TiO2. Methanol and formic and acetic acids were identified during the process. Selectivity toward methanol was found to be improved with the 10% Au/BB catalytic system. [ABSTRACT FROM AUTHOR]

This paper puts forward a generic methodological framework to holistically assess WtE technologies based on the PROMETHEE approach. In addition to environmental and economic aspects, the method focuses on large-scale applicability and social preference, thus adopting economic, environmental, social, and technological criteria. Three data sources are selected, namely the scientific literature, a public survey, and an experts' opinion survey, which is a novel combination with the aim to cover public consensus, technological applicability, and to provide alternative data sources for the economic and environmental criteria, thus enriching the methodology with the input of location specific data. The demonstration of the applicability of the proposed methodology is realized at a national level for the case of Greece. Anaerobic Digestion is shown to be the most preferable choice, recognized for its cost-effectiveness and lower environmental burden to other WtE technologies (i.e., gasification, pyrolysis, incineration). When all criteria are evaluated with equal weights, anaerobic digestion greatly outperforms incineration (net flow 0.833 versus 0.1667), while incineration only becomes the most preferred choice if the social criterion is in high focus (i.e., over 63% weight). [ABSTRACT FROM AUTHOR]

The purpose of this research is to investigate a variety of approaches to the conversion of biomass, with a particular emphasis on employing anaerobic digestion and biogas upgrading systems. An analysis of the existing technologies is performed, with a focus on highlighting the benefits and downsides of each alternative. In order to assess the effects of nitrogen and oxygen in the biogas on the cryogenic distillation process, an investigation is being carried out. The findings suggest that the presence of these two chemical species in the biogas necessitates the final condensation of methane in order to separate them from one another. In conclusion, a qualitative economic analysis is carried out in order to ascertain the most cost-effective strategy that can be implemented in a typical Italian installation. According to the assumptions that were used, membrane separation is the solution that offers the most cost-effectiveness. [ABSTRACT FROM AUTHOR]

Pyrolysis is a recognized alternative for the sustainable management of contaminated organic waste, as it yields energy-rich gas, oil, and a carbon-rich biochar product. Low-volatility compounds, however, such as heavy metals (HMs; As, Cd, Cu, Cr, Ni, Pb, and Zn) typically accumulate in biochars, limiting their application potential, especially for soil improvement. The distribution of HMs in pyrolysis products is influenced by treatment temperature and the properties of both the HMs and the feedstock. There is a significant knowledge gap in our understanding of the mass balances of HMs in full-scale industrial pyrolysis systems. Therefore, the fate of HMs during full-scale relevant pyrolysis (500–800 °C) of seven contaminated feedstocks and a clean wood feedstock were investigated for the first time. Most of the HMs accumulated in the biochar (fixation rates (FR) >70%), but As, Cd, Pb, and Zn partly partitioned into the flue gas at temperatures ≥ 600 °C, as demonstrated by FRs of <30% for some of the feedstocks. Emission factors (EFs, mg per tonne biochar produced) for particle-bound HMs (<0.45 µm) were 0.04–7.7 for As, 0.002–0.41 for Cd, 0.01–208 for Pb, and 0.09–342 for Zn. Only minor fractions of the HMs were found in the condensate (0–11.5%). To investigate the mobility of HMs accumulated in the biochars, a novel leaching test for sustained pH drop (at pH 4, 5.5 and 7) was developed. It was revealed that increasing pyrolysis temperature led to stronger incorporation of HMs in the sludge-based biochar matrix: after pyrolysis at 800 °C, at pH 4, <1% of total Cr, Cu, Ni, and Pb and < 10% of total As and Zn contents in the biochars were leached. Most interestingly, the high HM mobility observed in wood-based biochars compared to sewage-sludge-based biochars indicates the need to develop specific environmental-management thresholds for soil application of sewage-sludge biochars. Accordingly, more research is needed to better understand what governs the mobility of HMs in sewage-sludge biochars to provide a sound basis for future policy-making. [ABSTRACT FROM AUTHOR]

In this study, natural rubber (NR)/polybutadiene rubber (PB) blend-based composites were prepared using graphene as a partial replacement for carbon black (CB) in different parts per hundred rubber (phr) percentages. In a previous study, the vulcanization characteristics, viscoelastic behavior, and static mechanical properties were reported, and the compound labeled as compound 2 (with 2.5 phr of graphene and 52.5 phr of carbon black) showed optimum properties. Herein, we report the dynamic mechanical properties and the transport properties of the formulations to establish further characterization of the compounds. Three different organic solvents comprising benzene, toluene, and xylene were employed to analyze the sorption characteristics. The obtained data were also modeled with different theoretical predictions. The dynamic mechanical properties showed that certain compounds can be considered to be green tire formulations, as there were appreciable changes in the tanδ values at different temperatures (−25 °C to 60 °C). The thermogravimetric analysis showed that compound 2, with 2.5 phr of graphene, has a higher t50 value among the studied formulations, which indicates higher thermal stability than the base compound. The partial replacement of 2.5 phr of graphene in place of carbon black (total 55 phr) led to appreciable improvements in terms of thermal stability, transport properties, and dynamic mechanical properties. [ABSTRACT FROM AUTHOR]

Anaerobic digestion (AD) is a widely applied technology for renewable energy generation using biogas as energy vector. The existing microbial consortium in this technology allows for the use of several types of biomass as substrates. A promising alternative for the production of high-value products (e.g., mixed volatile fatty acids–VFAs, hydrogen) is the use of modified AD. There are several techniques to achieve this objective by modifying the operating conditions of the process. The literature has described the best AD routes for generating renewable energy or high-value products based on specific substrate types and operating conditions. Few studies have reported the integral fraction valorization of the AD process applying the biorefinery concept. This article provides an analysis of the different routes that favor the production of energy carriers and high-value products involving key issues related to operating conditions and substrates. Moreover, AD is addressed through the biorefinery concept. Finally, a case study is presented where renewable energy and mixed VFAs are generated by applying the biorefinery concept in a number of proposed scenarios using organic kitchen food waste (OKFW) as feedstock. The case study involves an experimental and simulation stage. Then, the economic feasibility of the proposed scenarios is evaluated. In conclusion, AD is a promising and economically feasible technology to produce valuable products from several types of waste materials. [ABSTRACT FROM AUTHOR]

Firefighters' occupational activity causes cancer, and the characterization of exposure during firefighting activities remains limited. This work characterizes, for the first time, firefighters' exposure to (coarse/fine/ultrafine) particulate matter (PM) bound polycyclic aromatic hydrocarbons (PAHs) and metal(loid)s during prescribed fires, Fire 1 and Fire 2 (210 min). An impactor collected 14 PM fractions, the PM levels were determined by gravimetry, and the PM-bound PAHs and metal(loid)s were determined by chromatographic and spectroscopic methodologies, respectively. Firefighters were exposed to a total PM level of 1408.3 and 342.5 µg/m3 in Fire 1 and Fire 2, respectively; fine/ultrafine PM represented more than 90% of total PM. Total PM-bound PAHs (3260.2 ng/m3 in Fire 1; 412.1 ng/m3 in Fire 2) and metal(loid)s (660.8 ng/m3 versus 262.2 ng/m3), distributed between fine/ultrafine PM, contained 4.57–24.5% and 11.7–12.6% of (possible/probable) carcinogenic PAHs and metal(loid)s, respectively. Firefighters' exposure to PM, PAHs, and metal(loid)s were below available occupational limits. The estimated carcinogenic risks associated with the inhalation of PM-bound PAHs (3.78 × 10−9 − 1.74 × 10−6) and metal(loid)s (1.50 × 10−2 − 2.37 × 10−2) were, respectively, below and 150–237 times higher than the acceptable risk level defined by the USEPA during 210 min of firefighting activity and assuming a 40-year career as a firefighter. Additional studies need to (1) explore exposure to (coarse/fine/ultrafine) PM, (2) assess health risks, (3) identify intervention needs, and (4) support regulatory agencies recommending mitigation procedures to reduce the impact of fire effluents on firefighters. [ABSTRACT FROM AUTHOR]

The proper disposal of antibiotic mycelial residue (AMR) is a critical concern due to the spread of antibiotics and environmental pollution. Pyrolysis emerges as a promising technology for AMR treatment. In this study, we investigated the effect of pyrolysis temperature on the thermal decomposition behavior and product characteristics of avermectin (AV) mycelial residues. Various characterization techniques were employed to analyze thoroughly the compositions and yields of the obtained gas, liquid, and biochar products. The results indicated that most of the organic matter such as protein, carbohydrate, and aliphatic compounds in AV mycelial residues decomposed intensely at 322 °C and tended to end at 700 °C, with a total weight loss of up to 72.6 wt%. As the pyrolysis temperature increased, the biochar yield decreased from 32.81 wt% to 26.39 wt% because of the enhanced degradation of volatiles and secondary reactions of the formed aromatic rings. Accordingly, more gas components were formed with the gas yield increased from 9.76 wt% to 15.42 wt%. For bio-oil, the contents were maintained in the range of 57.43–60.13 wt%. CO and CO2 dominated the gas components with a high total content of almost 62.37–97.54 vol%. At the same time, abundant acids, esters (42.99–48.85%), and nitrogen-containing compounds (32.14–38.70%) such as nitriles, amides, and nitrogenous heterocyclic compounds were detected for the obtained bio-oil. As for the obtained biochars, particle accumulation and irregular pores were presented on their bulk surface, which was primarily composed of calcium oxalate (CaC2O4) and calcium carbonate (CaCO3). This work can provide theoretical insights for the harmless disposal and resource recovery for AMR, contributing significantly to the field of solid waste reuse and management. [ABSTRACT FROM AUTHOR]

This document is an introduction to a special issue of the journal Eng, which focuses on experimental and theoretical research in engineering science and technology. The topics covered in the journal include various fields of engineering, such as electrical, chemical, mechanical, civil, and biomedical engineering, with an emphasis on contributing to the circular economy and sustainable development. The special issue contains 34 papers from authors in 25 countries, covering a range of cutting-edge developments in engineering. The author expresses gratitude to the contributors and hopes that the articles will be interesting and inspiring for readers, particularly young scholars. [Extracted from the article]

The present study aims to resolve the existing research gaps on olive pomace (OP) hydrochars application as a fuel by evaluating its molecular structures (FTIR and solid NMR analysis), identifying influential characteristics (Pearson correlation analysis), process optimization (response surface methodology), slagging–fouling risks (empirical indices), and combustion performance (TG-DSC analysis). The response surfaces plot for hydrothermal carbonization (HTC) of OP slurry performed in a pressure reactor under varied temperatures (180–250 °C) and residence times (2–30 min) revealed 250 °C for 30 min to be optimal conditions for producing hydrochar fuel with a higher heating value (32.20 MJ·Kg−1) and energy densification ratio (1.40). However, in terms of process efficiency and cost-effectiveness, the optimal HTC conditions for producing the hydrochar with the highest energy yield of 87.9% were 202.7 °C and 2.0 min. The molecular structure of hydrochar was mainly comprised of aromatic rings with methyl groups, alpha-C atoms of esters, and ether bond linkages of lignin fractions. The slagging and fouling risks of hydrochars were comparatively lower than those of raw OP, as indicated by low slagging and fouling indices. The Pearson correlation analysis emphasized that the enrichment of acid-insoluble lignin and extractive contents, carbon densification, and reduced ash content were the main pivotal factors for hydrochar to exhibit better biofuel characteristics for energy applications. [ABSTRACT FROM AUTHOR]

The European Union's energy policy favors increasing the share of renewable energy in total energy production. In this context, the co-digestion of various waste streams seems an interesting option. This study aimed to determine the effect of selected pretreatment methods on the efficiency and kinetics of the co-digestion process of poultry manure with sewage sludge and organic waste. This research was carried out in four stages: (1) the selection of the third component of the co-digestion mixture; (2) the determination of the most favorable inoculum-to-substrate ratio for the co-digestion mixture; (3) the selection of the most favorable pretreatment parameters based on changes in volatile fatty acids, ammonium nitrogen, extracellular polymers substances (EPS) and non-purgeable organic carbon (NPOC); and (4) the evaluation of anaerobic co-digestion based on the result of the BMP tests and kinetic studies. All the pretreatment methods increased the degree of organic matter liquefaction as measured by the NPOC changes. Waste with a high fat content showed the highest methane potential. The addition of grease trap sludge to feedstock increased methane yield from 320 mL/g VSadd to 340 mL/g VSadd. An optimal inoculum-to-substrate ratio was 2. The pretreatment methods, especially the thermochemical one with NaOH, increased the liquefaction of organic matter and the methane yield, which increased from 340 mL/g VSadd to 501 mL/g VSadd (trial with 4.5 g/L NaoH). [ABSTRACT FROM AUTHOR]

New bifunctional cobalt catalysts for combined Fischer–Tropsch synthesis and hydroprocessing of hydrocarbons containing Pt were developed. To prepare catalysts in the form of a composite mixture, the FT synthesis catalyst Co-Al2O3/SiO2 and ZSM-5 zeolite in the H-form were used as metal and acid components, respectively, with boehmite as a binder. The catalysts were characterized by various methods, such as XRD using synchrotron radiation, SEM, EDS, TEM and TPR. The effect of the Pt introduction method on the particle size and conditions for cobalt reduction was studied. The testing of catalysts in Fischer–Tropsch synthesis was carried out at a pressure of 2.0 MPa, a temperature of 240 and 250 °C, an H2/CO ratio of 2 and a synthesis gas volumetric velocity of 1000 h−1. It is shown that the method of introducing a hydrogenating metal by adjusting the nano-sized spatial structure of the catalyst determined the activity in the synthesis and group and fractional composition of the resulting products. It is established that the presence of Pt intensified the processes of synthesis and hydrogenation, including isomeric products, and reduced the content of unsaturated hydrocarbons. The application of Pt by impregnation onto the surface of the metal component of the catalysts provided the highest productivity for C5+ hydrocarbons, and for the acidic component, it enabled maximum cracking and isomerizing abilities. [ABSTRACT FROM AUTHOR]

Nowadays, we have observed the dynamic development of bio-heating plants that use wood biomass for heating or energy purposes. The result of this process is a reduction in carbon dioxide emissions as well as in the production of biomass ash (BA). Despite the waste nature of BA, it should be carefully analyzed and assessed for various applications, including environmental ones. Due to the features attributed to BA, including its alkaline reaction, the high capacity of its sorption complex, relatively low salinity, and significant content of macro- and microelements, a hypothesis was put forward in this work undertaken about the positive role of BA as an immobilizing factor for Cd-, Pb-, and Zn-contaminated soils. This research was based on a pot experiment in which four series were considered: (1) BA; (2) BA + Cd; (3) BA + Pb; and (4) BA + Zn. BA was used at doses of 30, 60, and 90 mg pot−1, and metals at doses of 2 mg Cd, 100 mg Pb, and 300 mg Zn kg−1 of soil. The test plant was corn grown for green mass. The study took into account the influence of BA on the content of the total forms of heavy metals (Metot) and their available forms (Meav). In the soil without the addition of metals, a significant increase in the content of Cdtot and Cdav, and a decrease in the content of Zntot were observed due to the application of BA. The addition of metals against the background of the BA used resulted in a significant increase in Cdtot, Pbtot, and Zntot, as well as an increase in the available forms of Pbav but a decrease in Znav. However, there was no significant increase in the Cdav content. The obtained results may indicate the potentially immobilizing role of BA only in the case of zinc. They may constitute the basis for further, more detailed research aimed at determining the role of BA in the immobilization of various metals in soil. [ABSTRACT FROM AUTHOR]

With the increase in the world population and economic activity, the production of sewage sludge has grown, and its management has become an environmental problem. The most traditional method of managing sewage sludge is to dispose of it in landfills and on farmland. One way to valorize sewage sludge is to use thermochemical conversion processes to produce added-value products such as biochar, biofuels, and renewable gases. However, due to the high moisture content, thermochemical conversion using processes such as pyrolysis and traditional gasification involves multiple pre-treatment processes such as material drying. Hydrothermal thermochemical processes usually require high pressures, which pose many challenges to their application on a large scale. In this work, the advantages and disadvantages of the different existing thermochemical processes for the recovery of sewage sludge were analyzed, as well as the resulting industrial and environmental challenges. A SWOT analysis was carried out to assess the different thermochemical processes in terms of technical feasibility, economic viability, and broader market considerations. [ABSTRACT FROM AUTHOR]

The escalating challenge of waste management demands innovative strategies to mitigate environmental impacts and harness valuable resources. This study investigates waste-to-energy (WtE) technologies for municipal waste management in Kočevje, Slovenia. An analysis of available waste streams reveals substantial energy potential from mixed municipal waste, biodegradable waste, and livestock manure. Various WtE technologies, including incineration, pyrolysis, gasification, and anaerobic digestion, are compared. The results show that processing mixed municipal waste using thermochemical processes could annually yield up to 0.98 GWh of electricity, and, separately, 3.22 GWh of useable waste heat for district heating or industrial applications. Furthermore, by treating 90% of the biodegradable waste, up to 1.31 GWh of electricity and 1.76 GWh of usable waste heat could be generated annually from biodegradable municipal waste and livestock manure using anaerobic digestion and biogas combustion in a combined heat and power facility. Gasification coupled with a gas-turbine-based combined heat and power cycle is suggested as optimal. Integration of WtE technologies could yield 2.29 GWh of electricity and 3.55 GWh of useable waste heat annually, representing an annual exergy yield of 2.98 GWh. Within the Kočevje municipality, this amount of energy could cover 23.6% of the annual household electricity needs and cover the annual space and water heating requirements of 10.0% of households with district heating. Additionally, CO2-eq. emissions could be reduced by up to 20%, while further offsetting emissions associated with electricity and district heat generation by 1907 tons annually. These findings highlight the potential of WtE technologies to enhance municipal self-sustainability and reduce landfill waste. [ABSTRACT FROM AUTHOR]

Mineralized materials are gaining increased interest recently in a number of fields, especially in bone tissue engineering as bone replacement materials as well as in the architecture-built environment as structural building materials. Until the moment, there has not been a unified sustainable approach that addresses this multi-scale application objective by developing a self-mineralized material with minimum consumption of materials and processes. Thus, in the current study, a hydrogel developed from sodium alginate, gelatine, and calcium phosphate dibasic (CPDB) was optimized in terms of rheological properties and mineralization capacity through the formation of hydroxyapatite crystals. The hydrogel composition process adopted a three-stage, thermally induced chemical cross-linking to achieve a stable and enhanced hydrogel. The 6% CPDB-modified SA–gelatine hydrogel achieved the best rheological properties in terms of elasticity and hardness. Different concentrations of epigallocatechin gallate were tested as well as a rheological enhancer to optimize the hydrogel and to boost its anti-microbial properties. However, the results from the addition of EPGCG were not considered significant; thus, the 6% CPDB-modified SA–gelatine hydrogel was further tested for mineralization by incubation in various media, without and with cells, for 7 and 14 days, respectively, using scanning electron microscopy. The results revealed significantly enhanced mineralization of the hydrogel by forming hydroxyapatite platelets of the air-incubated hydrogel (without cells) in non-sterile conditions, exhibiting antimicrobial properties as well. Similarly, the air-incubated bioink with osteosarcoma SaOs-2 cells exhibited dense mineralized topology with hydroxyapatite crystals in the form of faceted spheres. Finally, the FBS-incubated hydrogel and FBS-incubated bioink, incubated for 7 and 14 days, respectively, exhibited less densely mineralized topology and less distribution of the hydroxyapatite crystals. The degradation rate of the hydrogel and bioink incubated in FBS after 14 days was determined by the increase in dimensions of the 3D-printed samples, which was between 5 to 20%, with increase in the bioink samples dimensions in comparison to their dimensions post cross-linking. Meanwhile, after 14 days, the hydrogel and bioink samples incubated in air exhibited shrinkage: a 2% decrease in the dimensions of the 3D-printed samples in comparison to their dimensions post cross-linking. The results prove the capacity of the developed hydrogel in achieving mineralized material with anti-microbial properties and a slow-to-moderate degradation rate for application in bone tissue engineering as well as in the built environment as a structural material using a sustainable approach. [ABSTRACT FROM AUTHOR]