Search Results (10)

A thorough understanding of fuel behaviour is essential for designing and operating thermochemical systems. Thermogravimetric analysis (TGA) is among the most widely used fuel characterization methods, offering parameters like reactivity and ignition temperature, and enabling comprehensive fuel behaviour assessment through combined indices. This study critically examines the applicability of TGA-based indices for predicting coal performance in industrial processes such as gasification and combustion, where devolatilization, ignition, and burnout stages are key. TGA-derived data are compared with results from established methods, including drop tube furnace (DTF), pulse ignition (PI), and entrained flow reactor (EFR) tests. Findings indicate that the Volatile Matter Release Index (D₂) effectively predicts DTF behaviour (R² = 0.938, max residuals: 4.1 pp), proving useful for fast devolatilization analysis. The Flammability Index (C₁) and Ignition Index (C₃) correlate well with PI results (R² = 0.927 and 0.931, max residuals: 53.3a °C), making them reliable ignition indicators. While TGA tools showed limited accuracy in burnout prediction, the proposed Modified Burnout Characteristic Index (B_1′) achieved reasonable performance (R² = 0.734, max residuals: 0.062%∙°C⁻¹). Overall, selected TGA-based indices offer strong predictive potential for key thermochemical conversion stages. Full article

Incorporating a 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide-based derivative (1,4-bis(diphenoxyphosphoryl)piperazine, DIDOPO) in combination with modified calcium sulfate whiskers (MCSWs) improved the flame retardancy, thermal stability, and rheological properties of a polyethylene oxide (PEO) composite. The synergistic flame-retardant effect of DIDOPO and MCSW on the PEO system was investigated. After introducing 5 wt.% MCSW and 10 wt.% DIDOPO into PEO, the UL-94 rating of the composite reached V-0, and the limiting oxygen index was increased to 26.5%. Additionally, the peak and average heat release rates and total heat release of the PEO/10% DIDOPO/5% MCSW composite decreased by 38.9%, 22%, and 20.07%, respectively. The results of a thermogravimetric analysis (TGA) revealed that PEO/10% DIDOPO/5% MCSW displayed an improved initial thermal stability and rate of char formation compared to those of the PEO matrix. The results of TGA/Fourier transform infrared analysis indicated that the composites exhibited phosphorus-containing groups during thermal degradation, based on the characteristic absorption peaks, and increased amounts of gas-phase volatiles. The morphologies and structures of the residues indicated that the PEO/10% DIDOPO/5% MCSW blend was less stable than PEO during combustion. The MCSW mixture formed a denser, more continuous carbon layer on the composite surface during combustion. The rheological behavior indicated that the high complex viscosity and moduli of PEO/10% DIDOPO/5% MCSW promoted the cross-linking network structure of the condensed phase during combustion. MCSW exhibited an excellent flame retardancy and improved thermal stability, which are potentially promising for use in fire safety applications. Full article

This study investigated the influence of particle size on combustion performance using equivalent characteristic spectrum analysis (ECSA) on a TG-MS platform. The experiments were conducted at heating rates of 10 °C/min and 20 °C/min for three granular coal types with particle sizes of 1 mm, 4 mm, and 8 mm. The results showed that the ignition temperature, burnout temperature, and burnout time generally increased with particle size, while the combustion characteristic index for the 8 mm particles was 28.81% lower than that for 1 mm particles. The particle size effects were more pronounced at lower heating rates. Combustion kinetics revealed that the pre-combustion endothermic stage had a significant impact on the ignition temperature, followed by the volatilization stage. For Shenmu bituminous coal (SBC), a 1 kJ/mol reduction in apparent activation energy during the endothermic stage increased the ignition temperature by 13.02 °C (10 °C/min) or 17.11 °C (20 °C/min). Similar trends were observed for Datong bituminous coal (DBC) and Jincheng anthracite coal (JAC). A gas product analysis indicated that the peak release temperatures rose with particle size, and particle size variations affected the maximum release rates and combustion stage duration. Smaller particles generally released less NO during combustion. Full article

A simple and innovative method was introduced for the production of green and recoverable flame-retardant cotton fabrics, where sulfonated cotton fabric (COT-SC) was synthesized by oxidizing cotton fabric with sodium periodate, followed by a sulfonation step with sodium bisulfite to provide active sites, which further chelated barium ions (Ba²⁺) to achieve flame retardancy. The morphological and structural characterizations of the fabricated cotton fabrics (COT-SC-Ba) demonstrated that the cleavage of C₂-C₃ free hydroxy groups within the cellulose macromolecule was chemically modified for grafting a considerable number of sulfonic acid groups, and Ba²⁺ ions were effectively immobilized on the macromolecule of the cotton fabric through a chelation effect. Results from cone calorimeter tests (CCTs) revealed that COT-SC-Ba became nonflammable, displayed a delayed ignition time, and decreased the values of the heat release rate (HRR), total smoke release (TSR), effective heat of combustion (EHC), and CO/CO₂ ratio. TG/DTG analysis demonstrated that COT-SC-Ba possessed greater thermal stability, fewer flammable volatiles, and more of a char layer during burning than that of the original cotton fabric. Its residual mass was increased from 0.02% to 26.9% in air and from 8.05% to 26.76% in N₂, respectively. The COT-SC-Ba not only possessed a limiting oxygen index (LOI) of up to 34.4% but could also undergo vertical burning tests evidenced by results such as the non-afterflame, non-afterglow, and a mere 75 mm char length. Those results demonstrated that the combination of SO₃⁻ and Ba²⁺ promoted the formation of a char layer. Moreover, cotton fabric regained its superior flame retardancy after being washed and re-chelated with Ba²⁺. Additional characteristics of the cotton fabric, such as the rupture strength, white degree, and hygroscopicity, were maintained at an acceptable level. In conclusion, this research can offer a fresh perspective on the design and development of straightforward, efficient, eco-friendly, and recoverable fire-retardant fabrics. Full article

Co-pyrolysis technology is considered to be one of the most promising methods for the sustainable utilization of biomass wastes, as it can realize waste reduction and convert wastes into high-value-added products with little impact on the environment. The evaluation of thermal characteristics and product properties is necessary for understanding this technique. In this paper, thermal characteristics and kinetic and thermodynamic analysis during the co-pyrolysis of mushroom residue (MR) with pine sawdust (PS) or wheat straw (WS) were investigated in a TGA. The carbon structure and surface textures of co-pyrolytic char were explored using Raman spectroscopy and a scanning electron microscope. As the PS or WS mass ratio increased, the devolatilization index increased obviously, indicating that volatile release was promoted and concentrated. Weak interactions were observed between 250 and 400 °C during the co-pyrolysis process, which primarily affected the mass transfer, resulting in a change in the thermal decomposition temperatures and rates. The interactions had no prominent influence on the volatiles’ yields. The non-additive performance of average activation energies for the blends was observed due to the interactions, and the lowest average activation energy was obtained when the PS or WS mass ratio was 50%. The lower average pre-exponential factor of the blends indicated the reduced complicacy of the pyrolysis reaction. The relatively small deviation between the activation energy and enthalpy change (4.94–5.18 kJ·mol⁻¹) signified the energy sensitivity of product formation. PS promoted the formation of small aromatic rings (<6 fused rings) in co-pyrolytic chars, whereas WS favored the production of larger rings (≥6 fused rings). The surface textures of the co-pyrolytic chars became porous, and the greater fractal dimensions of the surface morphology for the co-pyrolytic chars indicated that the char surface became irregular and rough. Full article

As the third-largest maize-producing province in China and a typical arid and semi-arid region, quantitatively evaluating the carbon and nitrogen footprints of maize production and their dominant factors is of great significance in guiding the high-yield, low-carbon, and sustainable development of maize production in the Inner Mongolia Autonomous Region. This study quantitatively evaluated the interannual evolution characteristics of the carbon and nitrogen footprints in maize production and their dominant factors in Inner Mongolia from 2003 to 2022 based on statistical yearbook data and emission parameter models. The results showed that from 2003 to 2022, the maize planting area, yield, and total yield in Inner Mongolia all increased, with an average annual increase of 97 kg ha⁻¹ in yield and 1.23 × 10⁶ Mg in total yield. The carbon and nitrogen footprints of Inner Mongolia maize production over the past 20 years had overall decreasing trends, while the nitrogen fertilizer bias productivity, net ecosystem carbon balance, and sustainability index had increasing trends. Carbon footprint reduced by an average of 5.2 kg CO₂ eq Mg⁻¹ per year, and nitrogen footprint reduced by an average of 0.21 g N eq kg⁻¹ per year. Currently, the transportation and production of fertilizer and field application of N fertilizer are the main controlling factors of GHG emissions from maize production. NO₃⁻-N, NH₄⁺-N leaching, and NH₃ volatilization from field application of N fertilizer are the main sources of reactive N losses. The application of simplified processes, such as phased regulation of nitrogen and controlled-release fertilizers, as well as conservation tillage, have broad prospects for emission reduction in maize production in Inner Mongolia. Full article

The pouring of sand casting is accompanied by severe heat conduction, and there is an urgent need to investigate the pyrolysis properties of foundry sand. The main purpose of this study was to investigate the pyrolysis behaviors of resin sand, including precoated sand (PCS), hot box sand (HBS), and warm box sand (WBS), at heating rates of 20 °C/min, 30 °C/min, and 40 °C/min in nitrogen and air atmospheres. The mass loss of the resin sand was monitored continuously with a simultaneous thermal analyzer, and the kinetic parameters of the resin sand were calculated based on the Coats–Redfern method and thermal data. The average mass loss of the resin sand during pyrolysis was 3.03%, which was much smaller than that of the other sands. The volatile release characteristic index of resin sand could not be calculated based on this concept. To solve this issue, the term T_stv/m_loss was established, and its value was determined. With increasing heating rates from 20 °C/min to 30 °C/min and from 30 °C/min to 40 °C/min, the mass losses of the resin sand increased by 0.79% and 0.64%, respectively, and the volatile release characteristic indices of the resin sand increased by 3.8 × 10⁻¹⁰ and 1.06 × 10⁻⁹, respectively. In addition, the mass losses and volatile release characteristic indices of resin sand in an air atmosphere were greater than those in a nitrogen atmosphere. With increasing heating rate, the activation energy of the resin sand decreased in a nitrogen atmosphere. The findings concerning the thermal decomposition behaviors of resin sand provided a theoretical basis for the pouring step of the sand casting process. Full article

A 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO)-based derivative (PN-DOPO) combined with aluminium phosphates-coated sepiolite (Sep@AlPO₄) was used to improve the flame retardance, thermal stability and mechanical performances of poly (ethylene oxide) (PEO)/poly (butylene adipate-co-terephthalate) (PBAT) blends. The synergistic effects of PN-DOPO and Sep@AlPO₄ on flame-retarded PEO/PBAT composites were systematically discussed. Results indicated that introducing 5 wt% Sep@AlPO₄ with 10 wt% PN-DOPO into PEO/PBAT achieved a V-1 rating for the UL-94 test and increased the limiting oxygen index value to 23.7%. Moreover, the peak heat release rate (p-HRR), average HRR and total heat release values of PEO/PBAT/PN10%/Sep5% composites decreased by 35.6%, 11.0% and 23.0% compared with those of PEO/PBAT, respectively. Thermogravimetric analysis (TGA) results confirmed that PN-DOPO/Sep@AlPO₄ enhanced the initial thermal stability and char yield of PEO/PBAT matrix, and TGA/Fourier transform infrared spectrometry results revealed that the composites exhibited the characteristic absorption peaks of phosphorous-containing groups and an increase in gas-phase volatiles during thermal degradation. The morphological structures of the residues indicated that PN-DOPO and Sep@AlPO₄ mixtures produced a more dense and continuous char layer on the composite surface during burning. Rheological behaviour revealed that higher complex viscosity and modulus values of PEO/PBAT/PN-DOPO/Sep@AlPO₄ sample could also promote the crosslinking network structure of condensed phases during combustion. Furthermore, the PEO/PBAT/PN-DOPO/Sep@AlPO₄ composites exhibited superior elongation at break and flexural performance than the PEO/PBAT system. All results demonstrated that the PEO/PBAT system modified with PN-DOPO/Sep@AlPO₄ showed remarkable flame retardance, and improved thermal stability and mechanical properties, indicating its potential application in areas requiring fire safety. Full article

Thermal behavior and fire reaction properties of aerial glass fiber (GF)/bismaleimide (BMI) composites were tested using thermogravimetric analysis (TGA), thermogravimetric coupled with Fourier transform infrared spectroscopy (TG-FTIR), cone calorimeter, limiting oxygen index, and smoke density chamber. The results showed that the pyrolysis process was one stage in a nitrogen atmosphere with the prominent volatile components of CO₂, H₂O, CH₄, NO_x, and SO₂. The release of heat and smoke increased with the increase in heat flux, while the time required to reach hazardous conditions decreased. The limiting oxygen index decreased monotonically from 47.8% to 39.0% with increasing experimental temperature. The maximum specific optical density within 20 min in the non-flaming mode was greater than that in the flaming mode. According to the four kinds of fire hazard assessment indicators, the greater the heat flux, the higher the fire hazard, for the contribution of more decomposed components. The calculations of two indices confirmed that the smoke release in the early stage of fire was more negative under flaming mode. This work can provide a comprehensive understanding of the thermal and fire characteristics of GF/BMI composites used for aircraft. Full article

Eugenol has many functional properties for food and pharmaceutical purposes, especially as an antimicrobial agent. However, its use is constrained by its volatility and shelf life because it is easily degraded due to temperature, oxidation, and light. Research on encapsulation technology using biopolymers is still required to obtain the appropriate formulation in a eugenol delivery system. The aims of this research were to develop a new formulation of protein and polysaccharides in eugenol encapsulation and to determine the effect of eugenol and chitosan concentration on the characteristics of the emulsions and spray-dried powder produced. In this study, eugenol was encapsulated in whey protein–maltodextrin conjugates and chitosan through the double layer encapsulation method. The emulsions which were prepared with 2.0% eugenol were relatively more stable than those of 1.0% eugenol based on the polydispersity index and zeta potential values. Spray-dried powder which was prepared using an emulsion of 2.0% w/w eugenol and 0.33% w/w chitosan had the highest eugenol loading. The presence of chitosan resulted in more stable emulsions based on their zeta potential values, improved thermal stability of eugenol, increased eugenol loading to become twice as much as the loading obtained without chitosan, and modified release profile of eugenol from the spray-dried powders. Full article