Gas-phase Products Research Articles

Investigation on the effect of superheated water vapor on gas production from pyrolysis of long-flame coal

A self-developed superheated water vapor pyrolysis system was used to conduct superheated water vapor pyrolysis experiments on Tashan and Madaotou long-flame coals at 350–534 °C. The gas phase products were analyzed by gas chromatography. The yield and composition of gas phase pyrolysis products from two different long-flame coals were determined, and the role of superheated water vapor in the pyrolysis process was elucidated. The optimal temperature of the long-flame coal injection superheated water vapor mining technology was obtained through heat value analysis. The results showed that when the temperature of the superheated water vapor exceeded 400 °C, the yield and combustible components of the gas phase products rapidly increased. As such, the release rate reached 10–15 times that observed below 400 °C, and the components of the combustible gases, such as hydrocarbon gas and hydrogen, exceeded 80%. Superheated water vapor not only is an excellent heat and mass transfer medium, but also provides a reactant for the re-formation reaction of hydrocarbon gas. The pyrolysis of long-flame coal under superheated water vapor at 500 °C yielded the best economic benefits. The low calorific value of gas phase products produced via pyrolysis per ton of coal per unit time could reach 715 MJ/(t·h).

Atmospheric Fate of a New Polyfluoroalkyl Building Block, C3F7OCHFCF2SCH2CH2OH.

Many per- and polyfluoroalkyl substances (PFAS) have been regulated or phased-out of usage due to concerns about persistence, bioaccumulation potential, and toxicity. We investigated the atmospheric fate of a new polyfluorinated alcohol 2-(1,1,2-trifluoro-2-heptafluoropropyloxy-ethylsulfanyl)-ethanol (C3F7OCHFCF2SCH2CH2OH, abbreviated FESOH) by assessing the kinetics and products of the gas-phase reaction of FESOH with chlorine atoms and hydroxyl radicals. Experiments performed in a stainless-steel chamber interfaced to an FTIR were used to determine reaction kinetics and gas-phase products. We report reaction rate constants of k(Cl + FESOH) = (1.5 ± 0.6) × 10-11 cm3 molecule-1 s-1 and k(OH + FESOH) = (4.2 ± 2.0) × 10-12 cm3 molecule-1 s-1. This leads to a calculated FESOH gas-phase lifetime of 2.8 ± 1.3 days with respect to reaction with OH, assuming [OH] = 106 molecule1 cm-3. Gas-phase products of FESOH oxidation included at least two aldehydes, likely C3F7OCHFCF2SCH2C(O)H and C3F7OCHFCF2SC(O)H, and secondary products including COF2, SO2 and C3F7OC(O)F. Additional gas-phase experiments performed in a Teflon chamber were used to assess aqueous products by collecting gaseous samples offline into an aqueous sink prior to analysis with ultrahigh performance liquid chromatography-tandem mass spectrometry, resulting in four acidic products: C3F7OCHFCF2SCH2C(O)OH, C3F7OCHFCF2S(O)(O)OH, C3F7OCHFC(O)OH, and perfluoropropanoic acid (C2F5C(O)OH).

Synergistic inhibition of aluminum dust explosion by gas–solid inhibitors

The inhibition mechanism of gas-solid inhibitors on Al dust explosion was investigated experimentally in a closed cuboid chamber. The variation of parameters concerning flame propagation characteristic and explosion severity used to reflect the synergistic inhibition effect of gas-solid inhibitors on Al dust explosion were elucidated. The results showed that flame propagation velocity and explosion overpressure were inhibited with the increase of gas-solid inhibitors. The inhibition curves of gas-solid inhibitors within the experimental range were further obtained. The reason concerning the SEEP phenomenon was revealed through the GC-MS analysis. The combustion of ammonia enhanced the explosion overpressure when solid inhibitors performed at low concentration. The gas-phase product could be regarded as the inert gas as long as enough amount of inhibitors were added. To comprehend the inhibition mechanism of gas-solid inhibitors, X-ray diffraction was applied to figure out the crystal structure of explosion residue. The results indicated that both physical and chemical inhibition effects were imposed on Al dust explosion by gas-solid inhibitors, including endothermic decomposition, dilution of oxidizer, coverage of Al dust, and scavenger of free radicals. The results of this study will provide a scientific basis for the design of inhibition technology for the dust explosion.

Simultaneous ambient pressure x-ray photoelectron spectroscopy and grazing incidence x-ray scattering in gas environments

We have developed an experimental system to simultaneously measure surface structure, morphology, composition, chemical state, and chemical activity for samples in gas phase environments. This is accomplished by simultaneously measuring x-ray photoelectron spectroscopy (XPS) and grazing incidence x-ray scattering in gas pressures as high as the multi-Torr regime while also recording mass spectrometry. Scattering patterns reflect near-surface sample structures from the nano-scale to the meso-scale, and the grazing incidence geometry provides tunable depth sensitivity of structural measurements. Scattered x rays are detected across a broad range of angles using a newly designed pivoting-UHV-manipulator for detector positioning. At the same time, XPS and mass spectrometry can be measured, all from the same sample spot and under ambient conditions. To demonstrate the capabilities of this system, we measured the chemical state, composition, and structure of Ag-behenate on a Si(001) wafer in vacuum and in O2 atmosphere at various temperatures. These simultaneous structural, chemical, and gas phase product probes enable detailed insights into the interplay between the structure and chemical state for samples in gas phase environments. The compact size of our pivoting-UHV-manipulator makes it possible to retrofit this technique into existing spectroscopic instruments installed at synchrotron beamlines. Because many synchrotron facilities are planning or undergoing upgrades to diffraction limited storage rings with transversely coherent beams, a newly emerging set of coherent x-ray scattering experiments can greatly benefit from the concepts we present here.

Mechanism analysis of hydrogen production by microwave discharge in ethanol liquid

Microwave discharge in ethanol solution to produce hydrogen can obtain optimistic flow rate of hydrogen, because of the high mass transfer efficiency and water participation in the reaction. In this work, combined with liquid and gas products analysis, the main aim is to identify the reaction pathways of hydrogen production by microwave discharge plasma in ethanol-water mixtures. The features of radicals, gas-phase and liquid-phase products were investigated by the optical emission spectrum (OES) and gas chromatography (GC). The experimental results showed the gas-phase products included: H2, CO, CH4, C2H2, C2H4, C2H6, and CO2, and the liquid-phase products primarily included CH3CHO and CH3OH. By analysis, it is found that the amount of hydrogen production is closely related to the production of the intermediate product CH3CHO, and the OH radicals can inhibit the formation of solid carbon and by-product (C2H2), also promote the generation of hydrogen.

An experimental study of the gas-phase reaction between Cl atoms and trans-2-pentenal: Kinetics, products and SOA formation

The gas-phase reaction of trans-2-pentenal (T2P) with Cl atoms was studied at atmospheric pressure and room temperature. A rate coefficient of (2.56 ± 0.83) × 10-10 cm3 molecule-1 s-1 was obtained using the relative rate method and isoprene, cyclohexane and ethanol as reference compounds. The kinetic study was carried out using a 300-L Teflon bag simulation chamber (IMT Lille Douai-France) and a 16-L Pyrex cell (UCLM-Ciudad Real-Spain), both coupled to the Fourier transform infrared (FTIR) technique. Gas-phase products and secondary organic aerosol (SOA) formation were studied at UCLM using a 16-L Pyrex cell and a 264-L quartz simulation chamber coupled to the FTIR and gas-chromatography-mass spectrometry (GC-MS) techniques. HCl, CO, and propanal were identified as products formed from the studied reaction and quantified by FTIR, the molar yield of the latter being (5.2 ± 0.2)%. Formic acid was identified as a secondary product and was quantified by FTIR with a yield of (6.2 ± 0.4)%. In addition, 2-chlorobutanal and 2–pentenoic acid were identified, but not quantified, by GC-MS as products. The SOA formation was investigated using a fast mobility particle sizer spectrometer. The observed SOA yields reached maximum values of around 7% at high particle mass concentrations. This work provides the first study of the formation of gaseous and particulate products for the reaction of Cl with T2P. A reaction mechanism is suggested to explain the formation of the observed gaseous products. The results are discussed in terms of structure-reactivity relationship, and the atmospheric implications derived from this study are commented as well.

Flame Retarded Rigid Polyurethane Foams Composites Modified by Aluminum Diethylphosphinate and Expanded Graphite

Rigid polyurethane foam (RPUF) was an organic porous material, which was applied in many fields for excellent thermal insulation and mechanical properties, especially in building insulation. However, the poor fire performance significantly suppresses its further application. In this work, aluminum diethylphosphinate (ADP) combined with expanded graphite (EG) to form a synergistic flame retarded system, which was introduced to fabricate flame retarded rigid polyurethane foam composites (FR-RPUF) by one-step water-blown method. Furthermore, thermal insulation, thermal stability, fire performance, and decomposition products of RPUF and FR-RPUF composites were systematically investigated. It was found that FR-RPUF composites possessed LOI of 25.9 vol% with V-1 rating in UL-94 test when 10 php of ADP and 20 php of EG were added, which were better than RPUF composites with ADP or EG added alone. MCC test showed that RPUF/ADP24/EG6 had the lowest PHRR value of 159.85 W/g, which was 52.01 W/g lower than that of pure RPUF. Gas phase products investigation implied that the combination of ADP and EG could decrease toxic and combustible gases intensities, thus significantly enhancing fire safety of FR-RPUF composites. SEM test indicated that ADP and EG promoted the formation of dense and continuous char residue, which significantly inhibited heat and substance transfer in combustion, thus significantly enhancing fire performance of FR-RPUF composites.

Effect of relative humidity on SOA formation from aromatic hydrocarbons: Implications from the evolution of gas- and particle-phase species

Relative humidity (RH) plays a significant role in secondary organic aerosol (SOA) formation, but the mechanisms remain uncertain. Using a 30 m3 indoor smog chamber, the influences of RH on SOA formation from two conventional anthropogenic aromatics (toluene and m-xylene) were investigated from the perspective of both the gas- and particle- phases based on the analysis of multi-generation gas-phase products and the chemical composition of SOA, which clearly distinguishes from many previous works mainly focused on the particle-phase. Compared to experiments with RH of 2.0%, SOA yields increased by 11.1%–133.4% and 4.0%–64.5% with higher RH (30.0%–90.0%) for toluene and m-xylene, respectively. The maximum SOA concentration always appeared at 50.0% RH, which is consistent with the change trend of SOA concentration with RH in the summertime field observation. The most plausible reason is that the highest gas-phase OH concentration was observed at 50.0% RH, when the increases in gas-phase OH formation and OH uptake to aerosols and chamber walls with increasing RH reached a balance. The maximum OH concentration was accompanied by a notable decay of second-generation products and formation of third-generation products at 50.0% RH. With further increasing RH, more second-generation products with insufficient oxidation degree will be partitioned into the aerosol phase, and the aqueous-phase oxidation process will also be promoted due to the enhanced uptake of OH. These processes concurrently caused the O/C and oxidation state of carbon (OSc) to first increase and then slightly decrease. This work revealed the complex influence of RH on SOA formation from aromatic VOCs through affecting the OH concentration, partitioning of advanced gas-phase oxidation products as well as aqueous-phase oxidation processes. Quantitative studies to elucidate the role of RH in the partitioning of oxidation products should be conducted to further clarify the mechanism of the influence of RH on SOA formation.

Core-shell (Pt/Cu-TiO2)-Graphene Composites for Photocatalytic Conversion of CO2 Into Fuel

The global emissions of greenhouse gases continue to rise by about 3% each year. Increasing levels of CO2 in the atmosphere can be subsided through CO2 utilization technologies such as conversion into fuels or other value-added products. Unlike other CO2 conversion techniques, photocatalysis utilizes a renewable and sustainable form of energy and doesn’t increase net CO2 emissions. Various catalysts have already been tested in numerous studies for the photocatalytic reduction of gaseous CO2. However, researchers have yet to discover an efficient photocatalyst that can reduce CO2 to yield economic amounts of value-added products under the irradiation of solar light. Hence, in this study, an attempt to enhance the performance of TiO2-based photocatalysts for application in CO2 conversion was made. Surface modifications to help enhancement the visible light absorption and the charge separation of TiO2 photocatalysts were pursued. More specifically, a novel TiO2-based photocatalyst, incorporating copper (Cu), platinum (Pt), and reduced graphene oxide (rGO), was synthesized. Several advanced material characterization tools were employed to investigate the photocatalytic composite’s intrinsic and enhanced properties, including XRD, Raman, DRS, PL, TEM, STEM-EDX, FT-IR, etc. A custom-built reactor was used to test the photocatalytic activity of the catalyst in reducing CO2 under different parameters and conditions, most importantly is the photocatalytic reduction of liquid CO2, which has been rarely investigated. Gas-phase and liquid-phase products from the different photoreactivity tests were analyzed using GC-FID and HPLC, respectively. Results from this study show that CO2 was successfully reduced to CO, CH4, and other products under the irradiation of UV light, with the activity being much higher for liquid CO2 than for gaseous CO2. Furthermore, the proposed catalyst rGO-(Pt/Cu-TiO2) showed higher or comparable activity results during the photocatalytic reduction of liquid CO2 when compared to other tested catalysts, specifically in the formation of aldehydes.

The influence of terpenes on the release of volatile organic compounds and active ingredients to cannabis vaping aerosols.

Dabbing and vaping cannabis extracts have gained large popularity in the United States as alternatives to cannabis smoking, but diversity in both available products and consumption habits make it difficult to assess consumer exposure to psychoactive ingredients and potentially harmful components. This work studies the how relative ratios of the two primary components of cannabis extracts, Δ9-tetrahydrocannabinol (THC) and terpenes, affect dosage of these and exposure to harmful or potentially harmful components (HPHCs). THC contains a monoterpene moiety and has been previously shown to emit similar volatile degradation products to terpenes when vaporized. Herein, the major thermal degradation mechanisms for THC and β-myrcene are elucidated via analysis of their aerosol gas phase products using automated thermal desorption-gas chromatography-mass spectrometry with the aid of isotopic labelling and chemical mechanism modelling. Four abundant products – isoprene, 2-methyl-2-butene, 3-methylcrotonaldehyde, and 3-methyl-1-butene – are shown to derive from a common radical intermediate for both THC and β-myrcene and these products comprise 18–30% of the aerosol gas phase. The relative levels of these four products are highly correlated with applied power to the e-cigarette, which indicates formation of these products is temperature dependent. Vaping THC–β-myrcene mixtures with increasing % mass of β-myrcene is correlated with less degradation of the starting material and a product distribution suggestive of a lower aerosolization temperature. By contrast, dabbing THC–β-myrcene mixtures with increasing % mass of β-myrcene is associated with higher levels of HPHCs, and isotopic labelling showed this is due to increased reactivity of β-myrcene relative to THC.

Mechanistic studies of NH3-assisted reduction of mononuclear Cu(ii) cation sites in Cu-CHA zeolites

Spectroscopic, titrimetric, and gas-phase product analysis methods reveal a six-electron process for NH3-assisted reduction of mononuclear Cu(ii) sites to Cu(i) in Cu-CHA zeolites of different Cu(ii) site speciation and density.

A comparative and experimental study of the reactivity with nitrate radical of two terpenes: <i>α</i>-terpinene and <i>γ</i>-terpinene

Abstract. Biogenic volatile organic compounds (BVOCs) are intensely emitted by forests and crops into the atmosphere. During the night, they react very rapidly with the nitrate radical (NO3), leading to the formation of a variety of functionalized products including organic nitrates and to large amounts of secondary organic aerosols (SOAs). Organic nitrates (ONs) have been shown not only to play a key role in the transport of reactive nitrogen and consequently in the ozone budget but also to be important components of the total organic-aerosol mass, while SOAs are known to play a direct and indirect role in the climate. However, the reactivity of BVOCs with NO3 remains poorly studied. The aim of this work is to provide new kinetic and mechanistic data for two monoterpenes (C10H16), α- and γ-terpinene, through experiments in simulation chambers. These two compounds, which have very similar chemical structures, have been chosen in order not only to overcome the lack of experimental data but also to highlight the influence of the chemical structure on the reactivity. Rate constants have been measured using both relative and absolute methods. They were found to be (1.2±0.5)×10-10 and (2.9±1.1)×10-11 cm3 molecule−1 s−1 for α- and γ-terpinene respectively. Mechanistic studies have also been conducted in order to identify and quantify the main reaction products. Total organic nitrate and SOA yields have been determined. While organic nitrate formation yields appear to be similar, SOA yields exhibit large differences with γ-terpinene being a much more efficient precursor of aerosols. In order to provide explanations for this difference, chemical analysis of the gas-phase products was performed at the molecular scale. Detected products allowed for proposing chemical mechanisms and providing explanations through peroxy and alkoxy reaction pathways.

Decrease in carbon monoxide release and incomplete burning of fuel during activated combustion of coal

Combustion products and ash residue of bituminous coal modified with copper salts (Cu(NO3)2, Cu (CH3COO)2andCuSO4) in amount of 5 wt.% are studied. Application of additives to the coal samples is carried out by the method of incipient wetness impregnation with preliminary dissolution of the additive in aqueous-alcohol solution with a volume ratio of C2H5OH/H2O = 50/50. Combustion of coal samples is conducted in combustion chamber at temperatures of the heating medium of 500–700°C. Gas-phase combustion products are analyzed using a flow-through gas analyzer. Application of additives contributes to the reduction of incomplete fuel burning. The maximum change (7.1 times) has been recorded for the sample modified with Cu(NO3)2 at a heating medium temperature of 600°C. Analysis of gas-phase products has shown that activation of the combustion process with copper salts allows significantly reducing the volume of formed CO, providing more complete oxidation of combustible products to CO2.

Sequential coupling of thermal module into the reservoir simulator DMflow

In this work, we present a numerical framework for non-isothermal compositional compressible gas-water phase flow simulations in non-fractured and fractured porous media on structured and unstructured meshes. The framework is implemented as the simulator “DMflow”. The discretization of the mass conservation equations is based on the fully-implicit scheme and cell-centered finite-volume control-volume distributed multipoint flux approximation (CVD-MPFA) coupled with a lower dimensional fractured model. Similarly, the discretization of the energy equation is also based on the same method. The recent newly developed enthalpy model of CO2−CH4-H2S-N2-O2-brine system (Guo et al., 2019), which is validated within a wide temperature and pressure range, is used in the energy equation. Here, we present a sequential implicit method for the non-isothermal flow and avoid the simultaneous solution of the fluid flow primary variables and the temperature. We present the validation cases where the 1D and 2D results for non-isothermal carbon dioxide (CO2) injection into water obtained by the new implemented numerical framework are in agreement with the CMG-GEM. The simulation results of the injection of the CO2 into an aquifer shows the robustness of the method to produce gas phase behavior and temperature distribution in agreement with the literature. We also present a simulation case to demonstrate the capability of our simulator to model non-isothermal CO2 injection process into a fractured water saturated reservoir using an unstructured grid. The method is also then applied to simulate and compare the isothermal and the non-isothermal cases of injection of pure CO2 and impure CO2 into water reservoir with heterogeneity in porosity and permeability.

CO2-Free Hydrogen Production by Catalytic Pyrolysis of Hydrocarbon Feedstocks in Molten Ni–Bi

The catalytic decomposition of methane, propane, benzene, and crude petroleum was investigated between 900 and 1000 °C in molten metal bubble column reactors. The conversion to gas phase products a...

Pyrolysis Kinetic Study and Reaction Mechanism of Epoxy Glass Fiber Reinforced Plastic by Thermogravimetric Analyzer (TG) and TG-FTIR (Fourier-Transform Infrared) Techniques.

TG–FTIR combined technology was used to study the degradation process and gas phase products of epoxy glass fiber reinforced plastic (glass fiber reinforced plastic) under the atmospheres of high purity nitrogen. The pyrolysis characteristics of epoxy glass fiber reinforced plastic were measured under different heating rates (5, 10, 15, 20 °C min−1) from 25 to 1000 °C. The thermogravimetric analyzer (TG) and differential thermogravimetric analyzer (DTG) curves show that the initial temperature, terminal temperature, and temperature of maximum weight loss rate in the pyrolysis reaction phase all move towards high temperature, as the heating rate increases. Epoxy glass fiber reinforced plastic has two stages of thermal weightlessness. The temperature range of the first stage of weight loss is 290–460 °C. The second stage is 460–1000 °C. The above two weight loss stages are caused by pyrolysis of the epoxy resin matrix, and the glass fiber will not decompose. The dynamic parameters of glass fiber reinforced plastic were obtained through the Kissinger-Akahira-Sunose (KAS), Flynn–Wall-Ozawa (FWO) and advanced Vyazovkin methods in model-free and the Coats–Redfern (CR) method in model fitting. FTIR spectrum result shows that the main components of the product gas are CO2, H2O, carbonyl components, and aromatic components during its pyrolysis.

Long-lived species in plasma-activated water generated by an AC multi-needle-to-water discharge: effects of gas flow on chemical reactions

Plasma-activated water (PAW) represents a promising green antibacterial agent for biomedical and agricultural applications. In this study, a novel AC multi-needle-to-water discharge device was developed to investigate the effects of gas flow on the generation and chemical composition of PAW. It is shown that the concentrations of and N(III) ( and ) in the PAW both increased with an extension of the plasma-processing time and a reduction of the gas-flow rate. The absorption of gas-phase products carried by the gas flow from the discharge chamber was found to be beneficial for the generation of both and N(III) in the PAW at a gas flow rate of 20–60 L h−1, yet their concentrations were still lower than those without any feeding gas. As opposed to or N(III), the concentration in the plasma-activated phosphate buffer solution (PAPBS) increased under stronger gas flows and was almost unaffected by absorption in PAPBS. The pH value of PAW increased at higher gas flow rates. A comparison of the N(III) in PAW and PAPBS reflects the effects of the reactions of and in the two different working liquids. To quantify the effects of gas flow on the discharge characteristics, gas temperatures were calculated from the optical emission spectra and were proven to be flow-independent near the discharge channel. Fourier transform infrared (FTIR) measurements of the gaseous products during the discharge, and further analysis of possible reaction pathways indicated that by controlling the gas flow in the multi-needle-to-water discharge system, the concentration of long-lived species in PAW could be tuned, which might favor the generation of These findings contribute to a better understanding of effective electric discharge-related mechanisms for enhancing the biochemical and chemical activities of PAW.

The role of radiolysis in the modelling of C2H4O2 isomers and dimethyl ether in cold dark clouds

ABSTRACT Complex organic molecules (COMs) have been detected in a variety of interstellar sources. The abundances of these COMs in warming sources can be explained by syntheses linked to increasing temperatures and densities, allowing quasi-thermal chemical reactions to occur rapidly enough to produce observable amounts of COMs, both in the gas phase, and upon dust grain ice mantles. The COMs produced on grains then become gaseous as the temperature increases sufficiently to allow their thermal desorption. The recent observation of gaseous COMs in cold sources has not been fully explained by these gas-phase and dust grain production routes. Radiolysis chemistry is a possible non-thermal method of producing COMs in cold dark clouds. This new method greatly increases the modelled abundance of selected COMs upon the ice surface and within the ice mantle due to excitation and ionization events from cosmic ray bombardment. We examine the effect of radiolysis on three C2H4O2 isomers – methyl formate (HCOOCH3), glycolaldehyde (HCOCH2OH), and acetic acid (CH3COOH) – and a chemically similar molecule, dimethyl ether (CH3OCH3), in cold dark clouds. We then compare our modelled gaseous abundances with observed abundances in TMC-1, L1689B, and B1-b.

Flash Graphene from Plastic Waste.

In this work, an approach to upcycling plastic waste (PW) products is presented. The method relies on flash Joule heating (FJH) to convert PW into flash graphene (FG). In addition to FG, the process results in the formation of carbon oligomers, hydrogen, and light hydrocarbons. In order to make high-quality graphene, a sequential alternating current (AC) and direct current (DC) flash is used. The FJH process requires no catalyst and works for PW mixtures, which makes the process suitable for handling landfill PW. The energy required to convert PW to FG is ∼23 kJ/g or ∼$125 in electricity per ton of PW, potentially making this process economically attractive for scale-up. The FG was characterized by Raman spectroscopy and had an I2D/IG peak ratio up to 6 with a low-intensity D band. Moreover, transmission electron microscopy and X-ray diffraction analysis show that the FG is turbostratic with an interlayer spacing of 3.45 Å. The large interlayer spacing will facilitate its dispersion in liquids and composites. Analysis of FG dispersions in 1% Pluronic aqueous solution shows that concentrations up to 1.2 mg/mL can be achieved. The carbon oligomers that distilled from the process were characterized by Fourier transform infrared spectroscopy and have chemical structures similar to the starting PW. Initial analysis of gas-phase products shows the formation of considerable amounts of hydrogen along with other light hydrocarbons. As graphene is naturally occurring and shows a low toxicity profile, this could be an environmentally beneficial method to upcycle PW.

Organic Aluminum Hypophosphite/Graphitic Carbon Nitride Hybrids as Halogen-Free Flame Retardants for Polyamide 6.

The novel organic aluminum hypophosphite (ALCPA) and its hybrid (CNALCPA) with graphitic carbon nitride (g-C3N4) were successfully synthesized and applied as halogen-free flame retardants in polyamide 6 (PA6). Their structures, morphology, thermal stability, and fire properties were characterized. Results showed that both ALCPA and CNALCPA had good flame retardancy. PA6/CNALCPA composites achieved a high limited-oxygen-index (LOI) value of 38.3% and a V-0 rating for UL94 at 20 wt % loading, while PA6/ALCPA composites could reach a V-1 rating for UL94. The flame-retardant mechanism was also studied. On the one hand, the incorporation of g-C3N4 produced more gas-phase products, which indicated a gas-phase mechanism. On the other hand, g-C3N4 could catalyze the thermal degradation of ALCPA and PA6 to form a compact char layer that was evidence for a solid-phase mechanism. The tensile test of the PA6 composites also displayed good mechanical properties.