Search Results (724)

Ammonia borane is a promising hydrogen storage material due to its high hydrogen content, but its use as hydrogen carrier under thermal stimuli involves the production of several byproducts, such as borazine, reducing hydrogen purity and the overall efficiency. This work is focused on the use of high-boiling-point amines to modulate ammonia borane decomposition, aiming to enhance hydrogen release and suppress volatile N_xB_y species. Kissinger’s equation kinetics revealed that amines significantly influence the decomposition mechanism, and TGA-IR investigation showed a maximum of 2.4 wt.% of pure hydrogen release in the presence of triphenyl amine. Furthermore, the experimental data herein discussed, together with a computational study of activation energies, allowed us to derive a detailed mechanism that leads to a foundation for further advancement in the exploitation of ammonia borane as a hydrogen carrier, suggesting that the formation of linear species is anchored to amine over the release of borazine and production of poly borazine-like species. Full article

Direct thermal decomposition of rare-earth chlorides into rare-earth oxides (REOs) in a single step presents a short-process, wastewater-free, and environmentally friendly alternative to the conventional precipitation–calcination method, which produces large amounts of saline wastewater. While earlier reviews have primarily focused on summarizing reaction conditions and thermodynamic parameters, they have seldom discussed the critical variations in pyrolysis behavior across different rare-earth elements. This review highlights a novel classification of rare-earth chlorides into fixed-valence and variable-valence groups, revealing how their respective oxidation states govern thermodynamic stability, reaction pathways, and chlorine release behavior. Furthermore, a systematic comparison is provided on the effects of additives, temperature, and gas partial pressure on product purity, particle size, and microstructure, with particular attention to the mechanisms underlying oxychloride intermediate formation. Beyond fundamental reaction principles, this work uniquely evaluates the design and performance of existing pyrolysis reactors, outlining both opportunities and challenges in scaling up direct rare-earth chloride (RECl_x) pyrolysis for industrial REO production. By integrating mechanistic insights with reactor engineering considerations, this review offers advancements over previous descriptive summaries and proposes a strategic pathway toward sustainable rare-earth processing. Full article

The smoke toxicity of epoxy resin limits the application of its carbon fiber composites in marine interior structures. To address this issue, a novel epoxy resin (EZ) was synthesized by grafting phenyl propyl polysiloxane (PPPS) onto ortho-cresol novolac epoxy resin (EOCN), building upon the group’s earlier work on polysiloxane-modified epoxy resin (EB). The results confirmed successful grafting of PPPS onto EOCN, which significantly enhanced the thermal stability and char residue of EZ. Specifically, the peak heat release rate (PHRR), total heat release (THR), peak smoke production rate (PSPR), and total smoke production (TSP) of EZ were reduced by 68.5%, 35%, 73.1%, and 48.3%, respectively, attributable to the formation of a stable and compact char layer that suppressed smoke generation. By blending EZ with EB resin, a low-smoke epoxy system (LJF-2) was developed for prepreg applications. Carbon fiber composites (LJF-CF) prepared from LJF-2 exhibited minimal smoke emission and a unique bilayer char structure: a dense inner layer that hindered smoke transport and a thick outer layer that provided thermal insulation, delaying further resin decomposition. Silicon was uniformly distributed in the char residue as silicon oxides, improving its stability and compactness. Without adding any flame retardants or smoke suppressants, LJF-CF achieved a maximum smoke density (Ds,max) of 276.9, meeting the requirements of the FTP Code for ship deck materials (Ds,max < 400). These findings indicate that LJF-CF holds great promise for use in marine interior components where low smoke toxicity is critical. Full article

Microwave pretreatment (MWP) has emerged as a promising strategy to enhance the pyrolysis of lignocellulosic biomass due to its rapid, volumetric, and selective heating. By disrupting the recalcitrant structure of cellulose, hemicellulose, and lignin, MWP improves biomass deconstruction, increases carbohydrate accessibility, and enhances yields of bio-oil, syngas, and biochar. When combined with complementary pretreatments—such as alkali, acid, hydrothermal, ultrasonic, or ionic-liquid methods—MWP further reduces activation energies, facilitating more efficient saccharification and thermal conversion. This review systematically evaluates scientific progress in this field through bibliometric analysis, mapping research trends, evolution, and collaborative networks. Key research questions are addressed regarding the technical advantages of MWP, the physicochemical transformations induced in biomass, and associated environmental benefits. Findings indicate that microwave irradiation promotes hemicellulose depolymerization, reduces cellulose crystallinity, and weakens lignin–carbohydrate linkages, which facilitates subsequent thermal decomposition and contributes to improved pyrolysis efficiency and product quality. From an environmental perspective, MWP contributes to energy savings, mitigates greenhouse gas emissions, and supports the integration of renewable electricity in biomass conversion. Full article

Today, hydrogen is already widely regarded as up-and-coming source of energy. It is essential to meet energy needs while reducing environmental pollution, since it has a high energy capacity and does not emit carbon oxide when burned. However, for the widespread application of hydrogen energy, it is necessary to search new technical solutions for both its production and storage. A promising effective and cost-efficient method of hydrogen generation and storage can be the use of solid materials, including nanomaterials in which chemical or physical adsorption of hydrogen occurs. Focusing on the recommendations of the DOE, the search is underway for materials with high gravimetric capacity more than 6.5% wt% and in which sorption and release of hydrogen occurs at temperatures from −20 to +100 °C and normal pressure. This review aims to summarize research on hydrogen generation and storage using silicon nanostructures and silicon composites. Hydrogen generation has been observed in Si nanoparticles, porous Si, and Si nanowires. Regardless of their size and surface chemistry, the silicon nanocrystals interact with water/alcohol solutions, resulting in their complete oxidation, the hydrolysis of water, and the generation of hydrogen. In addition, porous Si nanostructures exhibit a large internal specific surface area covered by SiH_x bonds. A key advantage of porous Si nanostructures is their ability to release molecular hydrogen through the thermal decomposition of SiHx groups or in interaction with water/alkali. The review also covers simulations and theoretical modeling of H₂ generation and storage in silicon nanostructures. Using hydrogen with fuel cells could replace Li-ion batteries in drones and mobile gadgets as more efficient. Finally, some recent applications, including the potential use of Si-based agents as hydrogen sources to address issues associated with new approaches for antioxidative therapy. Hydrogen acts as a powerful antioxidant, specifically targeting harmful ROS such as hydroxyl radicals. Antioxidant therapy using hydrogen (often termed hydrogen medicine) has shown promise in alleviating the pathology of various diseases, including brain ischemia–reperfusion injury, Parkinson’s disease, and hepatitis. Full article

In this paper we study in detail the products formed during the process of water-assisted thermal oxidative decomposition (TOD) of polypropylene in the presence of pressurized oxygen. A set of techniques has shown that the main decomposition product in such a process is acetic acid with small amounts of other carboxylic acids (formic, propionic, succinic). The kinetics of carboxylic acid formation is studied by means of gas chromatography–mass-spectrometry as well as capillary electrophoresis, and the possible mechanisms behind the products formation are discussed. The role of water is considered based on the results obtained from substituting H₂O with D₂O in TOD. Compositions of residual oligomeric fractions as well as gas products are analyzed. Full article

The study presents the results of investigations into various types of anhydrous pyrolysis aimed at determining the kinetic parameters of hydrocarbon generation processes from source rocks. Surface outcrop samples from the Silesian, Dukla, and Skole units, characterized by a low level of thermal maturity, were used as experimental material. The samples predominantly represented the Menilite Beds from the aforementioned three units, but also included Istebna, Lgota, Verovice, and Spas beds, which exhibit significantly lower parameters that describe generation properties. The anhydrous pyrolysis experiments provided information on the rate of organic matter decomposition (TG/DSC), the degree of conversion (Rock-Eval), the quality of the obtained products (Py/GC), and the isotopic composition of the gaseous products (Py/GC/IRMS). Chromatographic analyses confirmed the oil-prone nature of kerogen contained in the Menilites from the Dukla Unit (Tylawa area), the Silesian Unit (Iwonicz fold), and the Skole Unit, revealing an equal share of all hydrocarbon fractions: C₁–C₉, C₁₀–C₁₅, and C₁₅₊. Through the integration of pyrolytic studies conducted on potential source rocks in the polish Outer Carpathians, a new type of information was obtained regarding the rate of organic matter decomposition, as well as the fractional and isotopic composition of the pyrolysis products. The set of obtained results was used to estimate the activation energy and characterize the potential source levels. The innovative aspect of this approach involved the isotopic characterization of gaseous products generated during thermal degradation of the source rocks. These data were subsequently used to establish genetic correlations with natural gases accumulated in hydrocarbon reservoirs of the Carpathian region. It has been demonstrated that pyrolysis using PY-GC-IRMS can yield results comparable to those obtained through generation in natural geological conditions. Full article

Blow flies (Diptera: Calliphoridae) play a crucial role in the decomposition process and serve as important forensic indicators due to their predictable colonization patterns. This review focuses on the dynamics of maggot masses, highlighting their ecological roles, thermoregulation, and implications for forensics. We summarize data on the self-organizing behavior of maggot masses, which is influenced by chemical cues and environmental factors. These masses can generate internal temperatures that exceed ambient levels by 10–20 °C, accelerating larval growth and impacting competition among individuals. This localized heating complicates the estimation of the postmortem interval (PMI), as traditional models may not take these thermal influences into account. Furthermore, maggot masses contribute significantly to nutrient cycling and soil enrichment, while the behavior of the larvae includes both cooperation and competition, which is influenced by the species composition present. This review highlights challenges in PMI estimation due to heat production but also discusses advancements in molecular tools and thermal modeling that enhance accuracy. Ultimately, we identify knowledge gaps regarding species diversity, microbial interactions, and environmental variability that impact mass dynamics, suggesting future research avenues that could enhance ecological understanding and forensic applications. Full article

Wellbore stability is a crucial factor affecting the safe exploitation of offshore natural gas hydrates. As a sustainable energy source, natural gas hydrate has significant reserves, high energy density, and low environmental impact, making it an important candidate for alternative energy. Although research on the stability of screen pipes during horizontal-well hydrate production is currently limited, its importance in sustainable energy extraction is growing. This study therefore considers the effects of hydrate phase change, gas–water seepage, energy and mass exchange, reservoir deformation, and screen pipe influence and develops a coupled thermal–fluid–solid–chemical field model for horizontal-well natural gas hydrate production. The model results were validated using experimental data and standard test cases from the literature. The results obtained by applying this model in COMSOL Multiphysics 6.1 showed that the errors in all simulations were less than 2%, with errors of 12% and 6% observed at effective stresses of 0.5 MPa and 3 MPa, respectively. The simulation results indicate that the presence of the screen pipe in the hydrate reservoir exerts little effect on the decomposition of gas hydrates, but it effectively mitigates stress concentration in the near-wellbore region, redistributing the effective stress and significantly reducing the instability risk of the hydrate reservoir. Furthermore, the distribution of mechanical parameters around the screen pipe is uneven, with maximum values of equivalent Mises stress, volumetric strain, and displacement generally occurring on the inner side of the screen pipe in the horizontal crustal stress direction, making plastic instability most likely to occur in this area. With other basic parameters held constant, the maximum equivalent Mises stress and the instability area within the screen increase with the rise in the production pressure drop and wellbore size, and the decrease in screen pipe thickness. The results of this study lay the foundation for wellbore instability control in the production of offshore natural gas hydrates via depressurization. The study provides new insights into sustainable energy extraction, as improving wellbore stability during the extraction process can enhance resource utilization, reduce environmental impact, and promote sustainable development in energy exploitation. Full article

Ammonium perchlorate (AP), as the most commonly used oxidizer in composite solid propellants, achieving its rapid decomposition at lower temperatures, is one of the key items used to improve propellant performance. Copper-based catalysts, due to their good performance in promoting AP decomposition and improving propellant combustion characteristics, are currently one of the most widely used catalyst types. However, the catalytic performance of copper-based catalysts for the decomposition of ammonium perchlorate, including the decomposition products, changes in the kinetic process during the decomposition, and the combustion process needs further research and clarification in terms of the influencing factors and mechanisms. Based on this question, to further analyze the essence of copper-based catalysts and the decomposition mechanism of CuO-catalyzed ammonium perchlorate, as well as its relationship with particle size, this paper compared and studied the effects of two different particle size CuO catalysts (small-diameter CuO-S and large-diameter CuO-L) on the thermal decomposition and combustion performance of AP. The results indicate that the decomposition of AP catalyzed by CuO mainly includes two stages: the initial low-temperature decomposition stage accelerated by the electron transfer mechanism and the subsequent second stage accelerated by the adsorption and conversion of intermediates by the catalyst. The two stages are controlled by different properties and are related to the particle size of the catalyst. This work provides in-depth research on CuO catalysts for the thermal decomposition of AP. Full article

The electrochemical decomposition of HI_x solution presents a promising alternative to overcome the challenges associated with HI thermal decomposition in the sulfur–iodine (S-I) cycle. In this study, constant current electrolysis and LSV tests were carried out for HI_x solution using an H-type electrolyzer at different current densities and anode solution compositions. The results showed that during the process of HI electrolysis, the dominant factor of voltage variation gradually changed from electrochemical polarization to ohmic polarization as the current density increased. When the I₂ concentration in the HI solution approached saturation, a voltage step occurred in the constant current electrolysis, reaching a maximum amplitude of 127.69%. The analysis indicated that the voltage step was related to the I₂ deposition on the electrode and PEM, which led to the simultaneous increase in activation polarization and ohmic polarization overpotential. The increase in I₂ concentration decreased the limiting diffusion current density; I₂ supersaturation led to the formation of an insoluble iodine film on the electrode surface, ultimately terminating the electrochemical reaction. This study provides guidance for the development of HI_x solution electrolysis technology for hydrogen production. Full article

To impart high flame resistance, enhanced thermal stability, and low dielectric properties to epoxy resin while maintaining good mechanical behaviors for high-end applications, a monomer (BZPN) containing the characteristic structure of benzoxazine, phthalonitrile, and trifluoromethyl was prepared and added into the Bisphenol A-type epoxy resin (DGEBA)/Dapsone (DDS) combination. The glass transition temperature (T_g) and carbon yield under a nitrogen atmosphere at 800 °C were found to significantly increase from 155 °C, 17.2% to 236 °C, 50.3%, respectively, for the neat EP/DDS and the BZPN-containing material. The UL-94 flammability rating achieved V-0 level when the BZPN content was 19.2 wt.% (EP-BZ-1). The thermal decomposition and flame retardancy mechanism were explored by TGA-FTIR, Raman, and XPS analysis. The fluorine-containing products were found in both the gas phase and the char residue, implying that the •CF₃ radicals played an important role in promoting the flame-retardant behaviors through a radical trapping mechanism. The dielectric constant and dielectric loss of the materials decreased as anticipated. In addition, mechanical testing of carbon fiber-reinforced composites showed that the BZPN-containing resin presented equivalent mechanical behaviors to the neat EP/DDS resin. The synthesized BZPN was proved to be an effective and promising additive for the epoxy-based composite. Full article

This study advances alkali-activated cementitious materials (AACMs) by developing a ground-granulated blast furnace slag/high-calcium fly ash (GGBS/HCFA) composite that incorporates Tuokexun desert sand and by establishing a clear linkage between activator chemistry, mix proportions, curing regimen, and microstructural mechanisms. The innovation lies in valorizing industrial by-products and desert sand while systematically optimizing the aqueous glass modulus, alkali equivalent, HCFA dosage, and curing temperature/time, and coupling mechanical testing with XRD/FTIR/SEM to reveal performance–structure relationships under thermal and chemical attacks. The optimized binder (aqueous glass modulus 1.2, alkali equivalent 6%, and HCFA 20%) achieved 28-day compressive and flexural strengths of 52.8 MPa and 9.5 MPa, respectively; increasing HCFA beyond 20% reduced compressive strength, while flexural strength peaked at 20%. The preferred curing condition was 70 °C for 12 h. Characterization showed C-(A)-S-H as the dominant gel; elevated temperature led to its decomposition, acid exposure produced abundant CaSO₄, and NaOH exposure formed N-A-S-H, each correlating with strength loss. Quantitatively, acid resistance was weaker than alkali resistance and both deteriorated with concentration: in H₂SO₄, 28-day mass loss rose from 1.22% to 4.16%, with compressive/flexural strength retention dropping to 75.2%, 71.2%, 63.4%, and 57.4% and 65.3%, 61.6%, 58.9%, and 49.5%, respectively; in NaOH (0.2/0.5/0.8/1.0 mol/L), 28-day mass change was +0.74%, +0.88%, −1.85%, and −2.06%, compressive strength declined in all cases (smallest drop 7.77% at 0.2 mol/L), and flexural strength increased at lower alkalinity, consistent with a pore-filling micro-densification effect before gel dissolution/cracking dominates. Practically, the recommended mix and curing window deliver structural-grade performance while improving high-temperature and acid/alkali resistance relative to non-optimized formulations, offering a scalable, lower-carbon route to utilize regional desert sand and industrial wastes in durable cementitious applications. Full article

Incineration is a widely adopted method for the disposal of waste energetic materials (SP). Nevertheless, this approach is associated with considerable thermal energy loss and significant environmental pollution. To address these limitations, this study proposes a co-pyrolysis process incorporating pine sawdust (SD) with SP. This technique utilizes the exothermic decomposition of energetic substances and the endothermic pyrolysis of biomass. Through this synergistic thermal interaction, the process enables efficient energy recovery and facilitates the resource valorization of SP. The pyrolysis kinetics and thermodynamics of SP, SD, and their blends were investigated. Synchronous thermal analysis examined the co-pyrolysis reaction heat at varying blend ratios, while the temperature’s effects on the gas–liquid–solid product distribution were explored. The results indicate that the apparent activation energy (E_a) required for co-pyrolysis of the SP and SD exhibits an initial increase followed by a decrease in both Stage 1 and Stage 2. Furthermore, the mean apparent activation energy (E_avg) during Stage 1 (FWO: 101.87 kJ/mol; KAS: 94.02 kJ/mol) is lower than that in Stage 2 (FWO: 110.44 kJ/mol; KAS: 100.86 kJ/mol). Co-pyrolysis reaction heat calculations indicated that SD addition significantly mitigates the exothermic intensity, shifts decomposition to higher temperatures (the primary exothermic zone shifted from 180–245 °C to 265–400 °C), and moderates heat release. Elevated temperatures increase the gas yield (CO and H₂ are dominant). High temperatures promote aromatic bond cleavage and organic component release; the char’s calorific value correlates positively with the carbon content. Higher co-pyrolysis temperatures increase the nitrogenous compounds in the oil, while the aldehyde content peaks then declines. This work proposes a resource recovery pathway for SP, providing fundamental data for co-pyrolysis valorization or the development of catalytic conversion precursors. Full article

This paper presents a detailed analysis of the thermal and flammability properties of polylactide- (PLA) and poly(ethylene terephthalate)- (PET) based polymer blends with biofillers, such as calcium lignosulfonate (CLS), lignosulfonamide (SA) and lignosulfonate modified with tannic acid (BMT) and gallic acid (BMG). Calorimetric studies revealed the presence of two glass transitions, one cold crystallization temperature, and two melting points, confirming the partial immiscibility of the PLA and PET phases. The additives had different effects on the temperatures and ranges of phase transformations—BMT restricted PLA chain mobility, while CLS acted as a nucleating agent that promoted crystallization. Thermogravimetric analyses (TGA) analyses showed that the additives significantly affected the thermal stability under oxidizing conditions, some (e.g., BMG) lowered the onset degradation temperature, while the others (BMT, SA) increased the residual char content. The additives also altered combustion behavior; particularly BMG that most effectively reduced flammability, promoted char formation, and extended combustion time. CLS reduced PET flammability more effectively than PLA, especially at higher PET content (e.g., 65% reduction in PET for 2:1/CLS). SA inhibited only PLA combustion, with strong effects at higher PLA content (up to 76% reduction for 2:1/SA). BMT mainly reduced PET flammability (48% reduction in 1:1/BMT), while BMG inhibited PET more strongly at lower PET content (76% reduction for 2:1/BMG). The effect of each additive also depended on the PLA:PET ratio in the blend. FTIR analysis of the char residues revealed functional groups associated with decomposition products of carboxylic acids and aromatic esters. Ultimately, only blends containing BMT and BMG met the requirements for flammability class FV-1, while SA met FV-2 classification. BMG was the most effective additive, offering enhanced thermal stability, ignition delay, and durable char formation, making it a promising bio- based flame retardant for sustainable polyester materials. Full article