Retarding Effect Research Articles

Alkoxysilyl derivative of carbamoylphosphonate as a flame retardant modifier of cotton fabrics

This research describes the synthesis of a silane derivative containing phosphorus and nitrogen atoms, leveraging their synergistic flame retardant effect through the incorporation of a PH bond to the isocyanate moiety. The synthesized silane featured alkoxysilyl groups, facilitating permanent bonds with the cotton fabric surface via hydrolysis. Cotton fabrics were modified using silane solutions of varying concentrations (2.5 %, 5 %, and 10 %) through a dip-coating process to determine the effect of the modifier amount on fabric properties. The modified fabrics were subjected to FT-IR, TGA, SEM, and EDS analyses, as well as microcalorimetric and LOI tests, to assess changes in flammability. FT-IR, SEM/EDS, and add-on analyses confirmed effective coverage of the cotton fabric with the flame retardant. Thermogravimetric tests indicated a significant reduction in the mass loss rate during thermal degradation. LOI analyses demonstrated a decrease in flammability (increase in LOI value), while microcalorimetric tests showed a substantial decrease in the heat release rate, correlating with increased modifier concentration on the fabric surface. Post-washing analyses revealed that, although some of the modifier was washed out, the samples still retained reduced flammability.

Short Glass Fiber Modifier Trisilanol-Isobutyl Polyhedral Silsesquioxane as Interfacial in Polypropylene Matrix: Effect of Flame Retardation and Mechanical Properties.

In the present work, short glass fiber is superficially modified with different concentrations of polyhedral oligomeric silsesquioxanes (Trisilanol-Isobutyl, TSI-POSS) for processing as a filler in a polypropylene matrix (PP). It is observed that increasing the amount of TSI-POSS increases the fracture point and tensile strength; the opposite is the case for the strength impact property. The behaviors of both dynamic mechanical and thermal analyses are also observed. The flame behavior, i.e., the burning rate, decreases with increasing TSI-POSS in the polymers.

Anomalous diffusion of self-propelled particles

Abstract The transport equation of active motion is generalised to consider time-fractional dynamics to describe the anomalous diffusion of self-propelled particles. In the present study, we consider an arbitrary active motion pattern modelled by a scattering function that defines the dynamics of the change of the self-propulsion direction. The exact probability density of the particle positions at a given time is obtained. From it, the time dependence of the firsts moments, i.e. the mean square displacement and the kurtosis for an arbitrary scattering function, are derived and analysed. Anomalous diffusion is found with a crossover of the scaling exponent from 2α in the short-time regime to α in the long-time one, 0 < α < 1 being the order of the fractional derivative considered. It is shown that the exact solution found satisfies a fractional diffusion equation that accounts for the non-local and retarded effects of the Laplacian of the probability density function through a coupled temporal and spatial memory function. Such a memory function holds the complete information of the active-motion pattern. In the long-time regime, space and time are decoupled in the memory function, and the time fractional telegrapher’s equation is recovered. The theoretical framework presented here can be applied as model of active motion that exhibits anomalous diffusion.

Synergistic effect of coal gangue on intumescent flame retardants

Abstract In order to improve the flame retardant properties of wood plywood, intumescent flame retardant coatings were prepared using melamine, borate, pentaerythritol and urea as the basic formulations and gangue as a modified additive. The flame retardancy of the samples was characterized using a cone calorimeter, scanning electron microscope, X-ray diffraction and thermogravimetric analysis. In addition, the study investigated the effect of gangue content on the properties of the prepared coatings. The results show that the doping of gangue in intumescent flame retardant coatings can improve the flame retardant effect of the coatings. Specifically, when the mass fraction of gangue was 8 wt%, the exothermic rate, total smoke production and total exothermic amount of the coating were significantly reduced. Moreover, the addition of gangue promoted the formation of a continuous and dense carbon layer structure during the combustion process of the coating, which produced a molten substance that effectively isolated oxygen and heat, thus strengthening the fire-retardant and heat-insulating properties of the coating. The results of this study provide valuable insights into the development of flame retardant coating formulations for wood plywood.

A bio‐based reactive P/N synergistic flame retardant for improving the fire safety and mechanical properties of epoxy resin

AbstractA high‐efficiency bio‐based P/N synergistic flame retardant (PVFD) is synthesized by combining furfurylamine and vanillin. The compound incorporates two different valence states of phosphorus as flame retardant structures, namely phenylphosphoryl dichloride (PPDC) and 9,10‐dihydro‐9‐oxa‐10‐ phosphophenyl‐10‐oxide (DOPO). PVFD and epoxy resin (EP) can cure into a cross‐linked network, thus not only improving the mechanical properties of EP but also achieving P/N synergistic flame retardant effects. Experimental results demonstrate that EP/PVFD‐5 obtained by adding 5 wt% of PVFD to EP passes the UL‐94 test and achieves V‐0 grade, whose limiting oxygen index (LOI) is up to 38.0%. EP/PVFD‐5 exhibits a decrease of 10.14% in peak heat release rate (PHRR), 16.90% in total heat release (THR), and 10.0% in total smoke release (TSP), while the residual carbon content increases by 8.5%. Additionally, the bending strength, bending modulus, tensile strength, and elongation at break of EP/PVFD‐5 increase by 3.9%, 4.9%, 45.1%, and 26.3%, respectively.Highlights The bio‐based raw materials we used are eco‐friendly and readily available. PVFD, an efficient P‐N synergistic compound, was synthesized. PVFD promotes the char formation of EP and dilutes the O2 concentration. PVFD does not cause the degradation of mechanical properties of EP.

Phosphonitrile hybrid metal-polyphenol network: An effective strategy for developing functional PVA composites with flame retardancy, antibacterial and UV resistance

The white pollution caused by non-degradable plastics poses a serious threat to human society and the environment, thus developing biodegradable material is urgent. In this work, a novel phosphonitrile hybrid metal-polyphenol network was constructed and used for the preparation of flame retardant, UV resistant and antibacterial multifunctional polyvinyl alcohol composite (PVA@HCPD-Ag). The limiting oxygen index (LOI) value of PVA@HCPD-Ag was improved to 33.5%, while the peak heat release rate (PHRR) and total heat release (THR) decreased by 35.62% and 47.76%. Besides, the ultraviolet protection factor (UPF) value of PVA@HCPD-Ag was significantly improved from 4.63 of the original PVA to 482.79, while the tensile strength was increased by 10.23%. Furthermore, the inhibition efficacy of PVA@HCPD-Ag for E. coli and S. aureus was up to 98.12% and 99.99%. This work explored the synergistic flame retardant effect of in-situ reduced Ag0 and phosphonitrile crosslinked polyphenol network and proposed an advanced strategy for developing high value-added functionalized PVA materials.

Synthesis of phosphorus fluorine containing polymers for flame-retardant, low surface energy and good dielectric performance epoxy resin electronic packaging materials

In order to satisfy the application of epoxy resin (EP) in high-end electronic packaging, phosphorus fluorine containing polymers were synthesized to simultaneously enhance the flame retardant, dielectric, and hydrophobic properties of EP. Through the reaction of 2-hydroxyethyl methacrylate and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO), a monomer named HEMA-P was synthesized. By copolymerizing (2,2,2-trifluoroethyl methacrylate and 1H, 1H, 7H-dodecafluoroheptyl methacrylate) with HEMA-P through the typical reversible addition-fragmentation chain transfer (RAFT) polymerization, two phosphorus fluorine containing polymer modifiers named 3FOP and 12FOP with different lengths of fluorine side chain were obtained. The flame-retardant level of FOP/EP composites reached V-1 level. The limited oxygen index (LOI) values of 3FOP/EP and 12FOP/EP composites (10 wt% additive amount) increased to 33.6 ± 0.5 % and 32.8 ± 0.3 %, respectively, with corresponding peak heat release rates (pHRR) decreased by 37.8 % and 33.2 % compared with neat EP, suggesting the FOP modified EP composites have good flame retardant and smoke suppression effects. The mechanical properties of the FOP/EP composites can also be improved. Notably, with the 10 wt% addition of 12FOPs, the water contact angle of 12FOP/EP composite reached 116.5°, which was 40.7 % higher than that of EP. Moreover, the dielectric constant decreased with the increasing fluorine content. The thermal stability and possible thermal degradation pathways of 3FOP and 12FOP were characterized by TG-IR, Py-GC/MS, and Raman spectroscopy. Based on experimental results, we innovatively revealed a phosphorus fluorine synergistic flame retardancy mechanism.

Elemental synergy flame retardant effect of Schiff base derivatives with similar chemical structure in TPU

To investigate the synergistic flame retardant effect of various elements, three flame retardants (SMAE, SDPS, SDPB) with similar chemical structure and containing different flame retardant elements were designed, synthesized, and applied to TPU. The test results showed that SMAE had a phosphorus-nitrogen synergistic effect and primarily exerted its flame retardant effect in the gaseous phase. The limiting oxygen index value of the TPU/4SMAE reached 32 % and passed UL 94 V-0 rating test. SDPB was obtained by introducing the boron, which further enhanced the flame retardant effect in the gaseous phase. The thermogravimetric combined with Fourier transform infrared spectroscopy results showed that TPU/4SDPB had the lowest intensity of gaseous phase products. With only 2 wt% SDPB, TPU can pass UL 94 V-0 test. Therefore, it also demonstrated that there was a good synergy between boron and phosphorus and nitrogen. SDPS was obtained by introducing the silicon, which can exert the flame retardant effect in the condensed phase. Scanning electron microscopy results showed that char layer of TPU/SDPS was the densest and silicon was retained as Si-O and Si-C in the char layer. However, the gaseous phase flame retardant effect of SDPS was restrained, and TPU/4SDPS only passes the V-2 rating. Hence, this work provided the direction of Schiff base derivatives flame retardants structure design in TPU.

Pearlite Growth Kinetics in Fe-C-Mn Eutectoid Steels: Quantitative Evaluation of Energy Dissipation at Pearlite Growth Front Via Experimental Approaches

Essential understanding of the pearlite growth kinetics is of great significance to predict the lamellar spacing and the resultant mechanical properties of pearlitic steels. In this study, a series of eutectoid steels with Mn addition up to 2 mass pct were isothermally transformed at various temperatures from 873 K to 973 K to clarify the pearlite growth kinetics and the underlying thermodynamics at its growth front. The microscopic observation indicates the acceleration in pearlite growth rate and refinement in lamellar spacing by decreasing the transformation temperature or the amount of Mn addition. After analyzing the solute distribution at pearlite growth front via three-dimensional atom probe, no macroscopic Mn partitioning across pearlite/austenite interface is detected, whereas Mn segregation is only observed at ferrite/austenite interface. Furthermore, in-situ neutron diffraction measurements performed at elevated temperatures reveal that the magnitude of elastic strain generated during pearlite transformation is very small. Based on the thermodynamic model, these experimental results are used to estimate the contribution of various factors to the total energy dissipation. Compared with the Mn-free alloy, the retardation effect of Mn addition on pearlite growth kinetics, which is partly due to the reduced driving force for pearlite growth, can be well explained by further considering the solute drag effect of Mn.

Fabrication of green montmorillonite modified bio-based rigid polyurethane foam with improved flame retardancy and enhanced mechanical properties

A low-carbon and sustainable green rigid polyurethane foam was prepared by compounding montmorillonite (MMT) with homemade barium phytate (BAPA). The flame retardancy, thermal stability and mechanical properties of the modified RPUFs investigated using the limiting oxygen index (LOI) method, cone calorimetry (CONE) and thermogravimetry. The results showed that the BAPA/MMT2 composite containing 2 wt% MMT had the highest LOI (25.1 %), and its peak heat release rate (PHRR) and total heat release (THR) were reduced by 14.33 % and 34.68 %, respectively, compared with that of the BAPA/MMT0 material without added MMT. In addition, the smoke production rate (SPR) and total smoke release (TSR) were reduced by 20.54 % and 30.77 %, respectively. BAPA/MMT2 had good flame retardancy and smoke suppression effect. The mechanical properties of BAPA/MMT2 with 2 wt% MMT were improved. The flame retardant mechanism confirmed that BAPA and MMT synergistically improved the quality of the carbon layer. At the same time, phosphorus-containing compounds (PO·), CO2 and water vapor were produced, which diluted the combustible gas in the gas phase and inhibit the flames spread. The current results provided a new strategy for the preparation of high-performance RPUFs.

Characterization of retardance of nondepolarizing and depolarizing media

A criterion for the characterization of the retardance effects produced by depolarizing and nondepolarizing linear media on interacting light is established based on Mueller matrices algebra. A consistent general description of retardance properties is performed by means of a serial decomposition of the Mueller matrix into three components, namely an element that encompasses the enpolarizing and depolarizing properties sandwiched by two elliptical retarders containing complete and decoupled information on retardance. The inherent ambiguity derived from the coincident formal structure of rotation matrices and circular retarders is removed though the introduction of the entrance and exit intrinsic reference frames, leading to the concepts of the intrinsic entrance and exit linear retarders, which are defined from the Mueller matrix itself and that are independent of the laboratory reference frames used to represent the incident and emerging polarized light beams, respectively.

The Effect of Growth Retardants on Reprodutive Efficiency and Yield of Groundnut (Arachis hypogaea L.)

A field experiment was carried out during Kharif, 2023 at dryland farm of S. V. Agricultural College, Tirupati campus of Acharya N. G. Ranga Agricultural University, Andhra Pradesh. The experiment was laid out in a split-plot design with three replications and two genotypes as main factor (G1- Dharani, G2- K-6), growth retardants as sub factor. The current experiment was conducted with an objective to study the impact of growth retardants on reduction of plant stature thereby enhancing the reproductive and assimilates partitioning efficiency along with yield. This article discusses various yield and reproductive efficiency related attributes of groundnut as influenced by growth retardants. The experimental results revealed that, the T5 (PBZ @ 250 ppm at 45 DAS) reported Maximum number of pegs per plant (58.50), number of pods per plant (28.89), shelling % (70.39) and harvest index (32.52 %). Among the two genotypes studied, G1 (Dharani) demonstrated more number of flowers (73), number of pegs per plant (50), number of pods per plant (26), shelling % (69) and harvest index (32 %).

Synthesis and Flame Retardant Behavior of Phosphorous- and Nitrogen-Containing Copolymer and Its Application in Polypropylene.

In this study, a 4-(hydroxymethyl)-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane 1-oxide (PEPA)-functionalized acrylate monomer, PEPAA, is designed and utilized for the synthesis of macromolecular flame retardants poly(PEPAA-co-AM) with varying PEPAA/AM ratio through copolymerization with acrylamide (AM). The poly(PEPAA-co-AM) is then incorporated into polypropylene (PP) to prepare PP/poly(PEPAA-co-AM) composites. The flame retardant effect of poly(PEPAA-co-AM) on PP is investigated using cone calorimetric test (CCT), and compared with that of PEPAA homopolymer (P-PEPAA), AM homopolymer (PAM), and blends of P-PEPAA/PAM. The results demonstrate that, in comparison with P-PEPAA, PAM, and blends of P-PEPAA/PAM, the incorporation of poly(PEPAA-co-AM) significantly enhances the flame retardancy of PP. Notably, the best flame retardancy is achieved when the ratio of PEPAA/AM copolymerization in poly(PEPAA-co-AM) is 2/8. The morphology and composition of residual chars from combustion are analyzed using SEM-EDS while the residual graphitization degree is examined through Raman spectroscopy. Additionally, TG-FTIR-MS is utilized to investigate the pyrolysis products in gas phase during thermal decomposition of poly(PEPAA-co-AM). Based on these experimental results, a flame retardant mechanism for poly(PEPAA-co-AM) is proposed. The PP/poly(PEPAA-co-AM) composites not only retain the excellent processing properties of pure PP but also exhibit enhanced mechanical properties.

Preparation of p-isopropylphenol polyoxyethylene ether and evaluation of its performance in concrete

P-isopropenylphenol polyoxylates (IPP-PE) were obtained by alkoxylation reaction using p-isopropylphenol phenol (IPP) and ethylene oxide (EO) as raw materials, and P-PCE polycarboxylic acid superplasticizer was obtained by free radical polymerization of ipp-PE and acrylic acid (AA) under the action of initiator and chain transfer agent. The effects of reaction temperature, acid-ether ratio, amount of chain transfer agent and initiator, and reaction time on the dispersion properties of superplasticizer were studied, and the molecular structure and microscopic morphology of the superplasticizer were characterized by FTIR,1HNMR, and SEM, and the influence of superplasticizer on concrete properties was evaluated by concrete performance tests. The test results determined that the optimal synthesis process of polycarboxylic acid superplasticizer was as follows: reaction temperature 40 °C, n(AA):n(IPP-PE)=6:1, chain transfer agent and initiator were 0.4% and 0.6% of the mass of large monomer, respectively, and the reaction time was 4.5h. The experimental results of the concrete performance test showed that the workability of concrete mixed with the self-made superplasticizer was excellent, and the initial and 1h longitudinal flowability of the superplasticizer reached 228 mm and 215 mm, respectively. The water reduction rate reached 36%, the 28d compressive strength reached 56.8 MPa, the initial slump reached 226 mm, and it had a certain retarding and air entrainment effect.

Local Permeability of a Metasurface in the MHz and GHz Ranges

The work is dedicated to the study of the magnetic response of a metasurface made of split ring resonators (meta-atoms) in the MHz and GHz ranges. A new method for calculating the local permeability of a metasurface in the MHz frequency range is proposed, taking into account the finite sizes of the elements, and for the first time, a result of high degree of accuracy matching with experimental values has been obtained. In the GHz range, additional factors such as the retardation effect, non-uniform current distribution in the meta-atom, and the complexity of the nature of meta-atoms’ interaction compared to the MHz range are also considered, in particular, the emergence of electrical interaction between them.

Optimizing acid microemulsions for cleaner gas production: A study on enhanced adsorption characteristics and implications in retardation

The ultralow interfacial tension between the oil and aqueous phases and the solubilization characteristics in microemulsion systems make them useful for surface cleaning and enhanced oil recovery applications. Microemulsions can form an adsorbed barrier on rock, reducing the acid-rock reaction rate. However, as acid retardation additives, the adsorption patterns of microemulsions are not clearly defined. In this study, microemulsions composed of various electrical surfactants, oil cores, and oil core additives were obtained, and their phase behaviors were investigated. Through adsorption and reaction experiments, cleaning microemulsions that enhance adsorption effects were identified, and their adsorption patterns and adaptability under flow conditions were evaluated. The results demonstrate that incorporating negatively charged polar compounds forms an enhanced adsorption microemulsion characterized by an average droplet size of less than 30 nm after mixing with the acid. The introduction of negatively charged polar compounds resulted in a 177 % increase in adsorption and an 81 % improvement in static retardation effect. Dynamic adsorption tests indicate that the pseudo-second-order model more accurately describes the kinetics of dynamic adsorption of microemulsions on rock surfaces. Under a fixed flow rate, the dynamic retardation rate increased with the concentration of the microemulsion. In practical acidification, the adsorption of microemulsions results mainly from combined electrostatic forces and fluid scouring, characterized by a continuous process of adsorption and desorption. Scanning electron microscope also confirmed that microemulsions can form an adsorptive film on the rock, reducing the acid-rock reaction rate. This study offers practical guidelines for the selection and application of retardation additives, aiming to enhance the ecological compatibility of chemical treatments in low-permeability limestone reservoirs.

Low Volume Gas-Flow Seeding For Highly Resolved Velocimetry Of The Boundary Layer

Ensuring fire safety in polymeric materials, which are inherently flammable but widely used in various industries, is of significant societal and economic importance. This study is part of a broader effort to understand polymer combustion and flame retardant effectiveness at a fundamental level. A major focus is the behavior of polymers burning along a vertical wall, a configuration chosen to study the release of flammable gases during pyrolysis, which contributes to the self-sustaining combustion reaction of a fire. This process occurs predominantly near the polymer surface within the boundary layer, requiring detailed analysis to evaluate flame retardant effectiveness. Our experimental setup replicates polymer pyrolysis using a flame-wall interaction burner with a vertical jet and a small inlet to mimic the release of flammable gases. The primary challenge in this setup is the introduction of seeding particles for Particle Image Velocimetry (PIV) measurements at low volume flow rates, which is complicated by reflections from the wall and the small flow scale relative to the main flow. To address this problem, we have developed a novel piezo-based ultrasonic seeder capable of controlled seeding at extremely low flow rates, thereby improving the accuracy of PIV measurements in non-reactive configurations. This seeder uses a piezo ring to excite a perforated metal membrane, forming uniform aerosol droplets. The design ensures a steady supply of particles, which is critical for evaluating boundary layer conditions. Our results demonstrate the seeder’s ability to maintain sufficient seeding density in the low volume flow region, facilitating detailed velocimetry analysis. The innovative seeder design proves effective in overcoming the limitations of conventional methods and provides new insights into polymer combustion processes and the role of flame retardants.

CT imaging to study meso-structure evolution of fractured oil shale during in-situ pyrolysis by high-temperature water vapor injection

Preceding the in-situ pyrolysis of oil shale, it is imperative to undertake reservoir fracturing and modification. The intricate evolution of meso-structures in both the fractured fissures and the surrounding rock matrix, constrained by in-situ stress during the pyrolysis process, plays a significant role in influencing the efficiency of heat transfer and the extraction effectiveness of produced materials.This article is based on the Micro-CT scanning technology to study the microscopic structural evolution patterns of high-temperature water vapor in-situ pyrolysis in oil shale with fractured fissures.The main research findings are as follows: Firstly, pre-existing fracturing fissures facilitate the formation and development of vertical bedding fractures.The vertical bedding fractures first appear at 300 °C, with a relative frequency of 1.35%, occurring earlier than the temperature at which such fractures emerge in intact oil shale.Secondly, at 450 °C,there is a pivotal transition point in the evolution of pore-fracture systems, shifting from a predominant increase in length to a predominant increase in aperture.Below 450 °C, changes in pore-fractures are primarily manifested in terms of quantity and length. However, after 450 °C, there is a noticeable increase in the aperture of pore-fracture systems.Thirdly,at temperatures within the range of 300 °C–350 °C, a closure phenomenon occurs in fractures, predominantly involving micro and medium fractures. This closure predominantly affects smaller fractures, providing only a moderate retardation effect on the development of larger fractures. Moreover, in the temperature range of 500 °C–550 °C, there is interconnection observed between large and medium fractures. Pre-existing multiple large fractures are consolidated into a singular interconnected large fracture.Finally, at 450 °C, there is a significant increase in the connectivity of pore-fracture networks. Below 450 °C, the primary connected flow pathways consist of pre-existing fracturing fissures and newly formed parallel bedding fractures. Beyond 450 °C, a complex network of pores takes over as the main interconnected flow channel.

Preparation and properties of toughened/flame‐retardant PA6/glass‐fiber composites reinforced by linear polyphosphazene elastomers

AbstractIn this study, the challenges of brittleness and flammability in Polyamide 6/glass fiber (PA6/GF) composites, which are crucial for heat‐resistant and stress‐bearing structural parts, are addressed. Polyphosphazene (PZ) elastomers, known for their exceptional flame‐retardant properties, are introduced to enhance the robustness and safety of these composites. Specifically, poly(diaryloxy)phosphazene (PDAP) and poly(difluoroalkoxy)phosphazene (PDFP) are utilized, both contributing to the improved toughness and flame resistance of the PA6/GF composites. Experimental results show that PDAP mainly played the role of solid‐phase flame retardant, while PDFP mainly acted the role of gas‐phase flame retardant. For PA/PZs composites without adding GF, PDFP plays a more efficient flame retardant effect than PDAP. By introducing 15 Vol% of PDFP, the limiting oxygen index (LOI) of the composite reached 26.1%, while the notched impact strength increased by 297%. For PA/PZs/GF composites, PDAP plays a better flame retardant role than PDFP. Under the action of 30 vol% GF and 15 vol% PDAP, the LOI of PA6/PDAP/GF composite reached 26.8%, and the notch impact strength improved to 18.7 kJ/m2, which is 165% higher than that of PA6/GF, and the UL‐94 test reaches V‐0 level. The findings of the study highlight the potential of PDAP and PDFP to act as dual‐function modifiers. These modifiers can considerably ameliorate both the impact resistance and flame retardancy of PA6 and PA6/GF composites. Such dual enhancement surpasses the typical trade‐offs seen in conventional composites, indicating a constructive direction for future material innovation.Highlights Polyphosphazenes simultaneously enhance PA6's toughness & flame resistance. Distinct flame retardant mechanisms found in PDAP and PDFP. GF presence alters PDAP and PDFP's flame retardant efficacy. PDAP shows superior flame resistance in GF‐reinforced PA6 composites. Without GF, PDFP outperforms PDAP in enhancing flame retardancy.

Early hydration of hot-stuffy steel slag-cement composite pastes: isothermal calorimetry and phase evolution

Hot stuffy self-disintegration has become an advanced and popular steel slag treatment method in recent years, presenting numerous advantages. Hot-stuffy steel slag (HSS) obtained by self-disintegration treatment technology with waste heat has different compositions and properties compared with ordinary steel slag (OSS). Although the properties of OSS as a mineral admixture have been reported by numerous articles, few researches focus on HSS, especially its effect on early cement hydration. In this paper, the early hydration of HSS-cement composite pastes is investigated from the insights of isothermal calorimetry and phase evolution. Effects of HSS on the setting time, hydration heat, reaction product, reaction degree, microstructure, and pore solution were systematically studied and compared with those of OSS. Results show that, unlike OSS, HSS hardly ever retards the early hydration of cement. This is caused by the differences in the composition of HSS and OSS due to the diversity in their production treatment processes. During the hot stuffy self-disintegration, the key retarding component in OSS, such as C12A7, reacts with water and their contents in HSS are reduced. It is found that hot stuffy self-disintegration is an effective method to mitigate the retardation effect of steel slag on the early hydration of cement. This study provides a better understanding of HSS, which is crucial for its utilization in cementitious materials.