Gaseous Research Articles

Functionalized Nanomaterials for Detecting Environmental Pollutants

AbstractThe environment consists of wide diversity, of which, an integral and most diversifying part is the living organisms, and hence it is imperative to design novel strategies that could alleviate pollutants and detect them at very minute levels. The functionalization of nanomaterials provides a very facile and efficient tool for the design of robust sensors that could detect pollutants that contaminate air, water, and soil. Because of their nanoscale size, these materials have enhanced surface‐to‐volume ratio, which in turn provide more reaction sites for the analyte interaction and enables highly specific and sensitive detection. Different nanomaterials like metal/metal oxide nanoparticles, quantum dots, carbon‐based nanomaterials, and miscellaneous nanomaterials like polymer, dendrimers, metal‐organic frameworks are functionalized with suitable ligands for efficient detection of a wide range of pollutants such as heavy metals, pesticides, industrial wastes, volatile organic compounds, toxic gases, and environmental pathogens with efficient level of sensitivity. In this review, we will briefly discuss different types of functionalized nanomaterials, strategies adopted for their functionalization, detection methodologies pursued for specific sensing and detection of different types of pollutants and their critical analysis, and future outlook.

Noble Gases, Carbon and Nitrogen Isotopes in Different Lithologies of Pesyanoe: Irradiation History and Impact Processes on the Aubrite Parent Body

Abstract We present the results of stepwise crushing and combustion analyses for noble gases, carbon and nitrogen in Pesyanoe aubrite pyroxene lithologies, composed of grey (Px-G) and light (Px-B) enstatites differing in the degree of impact processing and the number of inclusions. Our study identifies three main noble gas endmembers in Pesyanoe: a cosmogenic component, radiogenic 40Ar, and an endmember representing a mixture of solar wind and Q components in variable proportions. Based on petrographic and noble gas data we argue that these gases accumulated in the material during its regolith history and were later redistributed into gas inclusions/voids as the result of an impact event. During impact metamorphism, Px-G acquired its grey color and multiple gas inclusions were formed within it, more than in case of Px-B. Our study demonstrates for the first time: (1) The host phase of gases trapped during shock metamorphism are grains of rock-forming minerals, in particular Px-G, due to the formation of a large number of cracks in the direction of cleavage during brittle deformation, (2) The gas capture is associated not with the final stage of the formation of consolidated fragmental breccia, at which lithification of the fragments occurred, but with one of the intermediate impact events. High amounts of trapped and cosmogenic noble gases are released during the stepwise crushing—significantly higher than in case of any other studied aubrite. Some unusually high 36Ar/132Xe ratios (up to 54 780 versus 22 705 in the solar wind) were discovered during crushing of Px-G. Our preferable explanation of this phenomenon is a specific superposition of noble gas elemental fractionation processes related to the impact cratering of the Pesyanoe parent body. The carbon isotopic composition (δ13C = –21.2 ± 0.2‰, 1σ) is slightly heavier than that of the Bustee aubrite carbon. The combined use of different extraction methods made it possible to determine that the solar type and indigenous (δ15Nindig = –0.1 ± 3.2‰, 1σ) nitrogen components are located in the gas inclusions, whereas the extraneous nitrogen component (~+45‰) is chemically bound. The large cosmic ray exposure age variations (44 and 55 Ma in case of Px-G and Px-B, respectively) and the heterogeneous distribution of solar-type gases in Pesyanoe aubrite point to a diverse irradiation history of the material before breccia formation. Alternatively/additionally, cosmogenic gases (as well as solar and primordial) in Px-G may have became lost and/or partly redistributed into gas inclusions as a result of the impact event.

Development of Abraham model correlations for predicting the solubility of crystalline organic compounds and inorganic gases in ethyl formate

ABSTRACT Abraham model correlations are derived for predicting the solubility of crystalline organic compounds and inorganic gases dissolved in ethyl formate based on published experimental data gathered from the chemical literature. The mathematical expressions presented in the current study described the observed solubility data to within an overall standard deviation of 0.12 log units. Comparison of the Abraham model expressions for ethyl formate versus our recently published equations for ethyl acetate reveals that of the two organic solvents, ethyl acetate exhibits a better H-bond acceptor character, while ethyl formate engages in the stronger dipolar interactions with neighbouring solute molecules.

Detecting and sourcing GHGs and atmospheric trace gases in a municipal waste treatment plant using coupled chemistry and isotope compositions

Landfill operations and waste processing facilities are important and highly heterogeneous sources of both greenhouse gases (GHGs) and non-GHG air pollutants in the atmosphere. This arises the need for detailed apportionment of waste sources in order to locate and subsequently reduce emissions from landfills. Here, a time series of in situ measurements of atmospheric trace gases and spatial allocation of specific emission source types under different processing phases and environmental conditions were conducted in and in the surroundings of a Municipal Solid Waste Treatment Plant (MSWTP) in south-western Poland. Results revealed that several individual GHG sources dominated across the waste processing facility and that GHGs concentrations displayed spatial seasonality. An increase in the ground-level CH4 concentrations, from ∼ 30.3 to 56.3 ppmv, was observed close (∼5 – 10 m) to the major emission sources within the MSWTP. While hotspot areas generally yielded elevated CH4 concentrations near the soil surface, these were relatively low (2.4 to 8.9 ppmv) along the facility’s fence line. The study of the corresponding δ13C delineated the extent of dispersion plumes downwind emission hotspots, characterized by a 13C depletion (around 4.0 ‰) in the atmospheric CH4 and CO2. For CH4, emissions were isotopically discriminated between the extraction wells at active quarters/cells (δ13C = –58.3 ± 1.1 ‰) and biogas produced in the biological waste treatment installation (δ13C = –62.7 ± 0.7 ‰). Most of the trace compounds (non-methane hydrocarbons, halocarbons, oxygen-bearing organic gases, ketones, nitrogenous and sulphurous gases, and other admixture compounds) detected at the ground surface were linked to the CH4- and CO2-rich spots. Despite the relatively high variability in the concentrations of organic and inorganic compounds observed at the MSWTP active zones, our results suggest that they do not have a meaningful impact on the surrounding air quality.

Functionalized construction of multiple active centers for durability controlling during catalytic combustion of chlorinated aromatic hydrocarbons

The catalytic combustion of chlorine-containing VOCs primarily encounters the bottleneck of catalyst poisoning by chlorine, thereby impeding the further industrial application of this technology. The development of multi-active catalytic materials for discerning chlorine fixation, chlorine transfer, deep oxidation during elimination of chlorine-containing VOCs can mitigate catalyst chlorination and enhance stability. Herein, we utilizing LDHs as catalyst precursors and successfully synthesized flower-like Co2FexCr1-xOy catalyst with different functionalized reaction centers. The addition of Cr improved the surface lattice oxygen, oxygen vacancies, and acid sites of catalyst. The removal efficiency of CB can be achieved >90 % at 247 °C (WHSV = 33000 mL · g−1·h−1). The fixation of dissociated chlorine contributed by Cr not only enhances oxidation performance and directional adsorption of chlorine, but also improves carbon deposition resistance and catalyst sintering resistance significantly. Compared with Co2Fe1Oy, Co2Fe0.67Cr0.33Oy catalyst achieves a remarkable threefold reduction in surface carbon deposition. The DFT calculation revealed that water dissociation energy over the Co site is −0.72 eV, which is significantly lower than Fe (−0.59 eV) and Cr (−0.17 eV), facilitating water dissociation and subsequently removes a substantial amount of accumulated chlorine on Cr to form HCl. With the help of In situ DRIFT and GC/MS analysis, we found the efficient removal of chlorine atoms enhances the exposure of active sites on the catalyst surface with hydrolyzed hydroxyl group, which facilitating the conversion of aromatic hydrocarbons into a greater quantity of maleate and carboxylate species. This phenomenon is beneficial for the subsequent mineralization process of chlorobenzene. This work provide valuable insights for multi-active site catalysis mechanism in practical applications aimed at eliminating chlorinated organic waste gases from industrial emissions.

Effect of Ga Variation on the Bulk and Grain‐Boundary Properties of Cu(In,Ga)Se2 Absorbers in Thin‐Film Solar Cells and Their Impacts on Open‐Circuit Voltage Losses

ABSTRACTPolycrystalline widegap Cu(In,Ga)Se2 (CIGSe) absorbers for top cells in photovoltaic tandem devices can be synthesized via [Ga]/([Ga] + [In]) (GGI) ratios of > 0.5. However, the power conversion efficiencies of such high‐GGI devices are smaller than those of the record cells with GGI < 0.5. In the present work, the effects of the GGI ratio on various CIGSe material properties were studied and correlated with the radiative and nonradiative open‐circuit voltage (VOC) deficits of the thin‐film solar cells. Average grain sizes, grain boundary (GB) recombination velocities, fluctuations in luminescence energy distribution, barrier heights at GBs, effective electron lifetimes, and Urbach energies were investigated in five solar cells with GGI ratios from 0.13 to 0.83. It was found that the GGI variation affects GB recombination velocities, fluctuations in spatial luminescence distributions, the average grain size, the electron lifetime, and the Urbach energy. In contrast, the detected ranges of barrier heights at GBs are independent of the GGI ratio. Mainly Ga/In gradients give rise to substantial radiative VOC losses in all solar cells. Nonradiative VOC deficits are dominant especially for solar cells with GGI > 0.5, which can be attributed to low bulk lifetimes and enhanced recombination at GBs in CIGSe absorbers in this compositional range.

Exploring the use of ground-based remote sensing to identify new particle formation events: A case study in the Beijing area

New Particle Formation (NPF) is an important process of secondary aerosol production in the atmosphere, which has significant impacts on the Earth's radiation balance, air quality, and climate change. In this study, we develop a method to identify NPF events based on ground-based remote sensing. We propose a proxy to characterize NPF events utilizing ground-based remote sensing of gaseous precursors and aerosol optical depth (AOD). This proxy is applied to identify the NPF events in Beijing in the winter of 2022 and tested by comparison with in-situ observations of aerosol particle number size distributions (PNSD) from SMPS. The comparison shows that the NPF events for regional nucleation can be identified effectively when the threshold for sulfur dioxide and organic gases (i.e. formaldehyde) are determined as 0.44 × 10−4 and 1.07 × 10−4. Based on these thresholds, the NPF events can be identified at a high percentage (84 %) compared with in-situ observations. The relationship between identification of NPF events and meteorological conditions shows that NPF events in Beijing winter occurred more frequently under weather conditions with north-west wind direction, high wind speed and low relative humidity.

Heat transfer research on the cooling process of waxy crude oil storage in the vault tank based on VOF model

This paper focuses on the static cooling process for waxy crude oil stored in dome roof tanks. For the three phases of gas on top, liquid crude oil, and bottom water in storage tank, the VOF method is used to describe the evolution of physical quantities at the “oil–water”/“oil–gas” interface. The porous medium method is used to quantitatively characterize the sol–gel conversion process for waxy crude oil. A physical and mathematical models are established to describe the flow-heat transfer coupling behavior of the three-phase medium of crude oil, gas on top, and water at the bottom of the dome roof tank. In terms of the overall cooling process,The gas at the top of the tank has the simplest and fastest physical field evolution. It has the most uneven distribution (average temperature variance of 4 °C2), the strongest flow (average flow velocity of 0.4 m/s), the highest cooling rate (0.632 °C/h), and the lowest temperature (14.84 °C at the end). Its physical field is influenced by both the atmosphere and crude oil. The evolution of the physical field of crude oil is the most complex. It lags behind the gas at the top of tank and is directly effectted by it. Based on the evolution characteristics of the flow field of crude oil, the cooling process is divided into three stages: Stage I (0–––10 h) is the stage of convection generation and evolution in the crude oil region; Stage II (10 h − 34 h) is the stage of convection stability in the crude oil region; Stage III (after 35 h) is the stage of flow field transformation of crude oil. In stages I and II, the flow and momentum exchange at the oil–gas interface are significant. Crude oil is jointly influenced by the natural convection of the gas at the top of the tank and its own natural convection, forming a counterclockwise large vortex structure. The low-temperature area is near the central axis boundary of storage tank, oil–gas interface, and tank wall. The high-temperature area is within a range of 0.1 m − 3.3 m from the tank wall. After entering stage III, the flow and momentum exchange at the oil–gas interface weaken. The flow field of crude oil is only controlled by its own natural convection and transforms into a clockwise large vortex dominated. The low-temperature area is concentrated in the enclosed area of “oil–gas interface − tank wall” and “oil–water interface − tank wall”. The temperature field changes accordingly. Eventually, the high-temperature area is concentrated in the area slightly above the center of the tank. The physical field evolution of bottom water lags behind crude oil and is most unstable. Its cooling rate is 0.164 °C/h, slightly higher than crude oil’s 0.157 °C/h. The temperature is always slightly lower (33.47 °C at the end), and the physical field is the most uniform (average temperature variance of 0.0003 °C2), affected by the tank bottom environment and liquid crude oil.

Effective spin models and magnetic phases of an insulating bosonic ladder with unconventional synthetic flux

We investigate the Mott insulating phases of a two-component bosonic lattice gas in the presence of gauge field. Such a system is described by a two-leg ladder model with an unconventional flux. The synthetic flux is generated by the spin-dependent tunneling and the site-dependent spin-flip. In the Mott regime, these two effects lead to Dzyaloshinskii-Moriya (DM) interaction and an external field that is rotating in the xy-plane. We obtain a very general XYZ model with the DM interaction, the spiral field, and the transverse field. Various interesting magnetic Hamiltonians can be covered by adjusting lattice parameters. The DM interaction or the spiral field can lead to spiral order when they appear alone. The interplay of DM coupling and spiral field leads to the emergence of a new multi-frequency spiral order between the paramagnetic phase and the spiral ferromagnetic phase. Ground state phases are investigated by focusing on order parameters, spin-spin correlation functions, and structure factors. Calculations are performed by using time evolution block decimation (TEBD) based on matrix product state (MPS).

Fabrication of modified Sb2O3 nanospheres for the removal of hazardous malachite green organic pollutant and selective NO2 gas sensor

Sb2O3 and Ni modified Sb2O3 (Ni–Sb2O3) nanospheres were synthesized using low cost co-precipitation method and characterised using various instrumental methods such as X-ray Powder Diffraction (XRD), High Resolution Transmission Electron Microscopy (HR-TEM), Scanning Electron Microscopy (SEM), Energy dispersive X-ray spectroscopy (EDS), and Fourier-transform infrared (FT-IR) spectroscopy. The XRD pattern reveals cubic crystal lattice. The average size of Sb2O3 and Ni–Sb2O3 nanoparticles was calculated to be around 41 nm and 29 nm, respectively. The HR-TEM investigation of the Sb2O3 nanomaterial reveals homogeneous spherical balls with a fine dispersion. The random-shaped nanoparticles with porous surfaces and voids were revealed by SEM. EDS examination confirms the elemental composition of Sb (41.79 %) and O (58.21 %) in Sb2O3 and Sb (36.80 %), O (58.95 %), and Ni (4.25 %) in Ni–Sb2O3. Sb2O3 and Ni– Sb2O3 exhibit band gaps of 3.67 eV and 3.51 eV, respectively, according to UV–Vis analysis. The IR peaks 445.47, 642.18, and 745.18 in Sb2O3 and 438.72, 645.07, and 756.92 in Ni– Sb2O3 support the Sb–O bonding in the synthesized nanomaterials. The synthesized nanomaterials have been used for photocatalytic degradation of malachite green (MG) dye and sensing NO2, SO2, CO2, petroleum vapour and LPG gases. The MG dye was degraded 97.67 % in 120 min using Ni–Sb2O3 at optimized conditions (catalyst dose: 0.1 g/L to 0.3 g/L, pH: 7 and MG dye: 10 ppm). The gas sensing study showed that Ni–Sb2O3 sensor has greater sensitivity and selectivity for NO2 gas.

Bifacial and Angular‐Resolved Performance Characterization of Ultrathin Cu(In,Ga)Se2 Solar Cells Including Nanostructures

Bifacial solar cells experience growing interest not just for crystalline silicon photovoltaic modules. Thin‐film solar cells deposited on a transparent back contact bring inherent semitransparency, making them ideally suited for bifacial applications. Herein, a systematic investigation of bifacial measurement procedures is performed on semitransparent ultrathin Cu(In,Ga)Se2 (CIGSe) solar cells on transparent conductive oxide, including nanostructures. The measurements are further extended by angular‐resolved performance studies. The bifaciality of the samples is determined to be ≈80% in current and ≈65% in power, and enables the calculation of an equivalent irradiance for solar cell testing under >1 sun front illumination only. The results are compared to bifacial operation, i.e., simultaneous front and rear irradiance, and to the summation of individual front and rear performance measurements up to 1 sun. It is revealed that highly similar results can be obtained for these approaches and that the integration of nanostructures supports device stabilization. Particularly, the higher (75 nm) SiO2 nanomeshes can enable performance enhancement. Furthermore, the angular‐dependent behavior follows the expected trend of reduced illumination intensity according to the cosine of the incident angle. In these findings, the suitability of semitransparent ultrathin CIGSe solar cells for bifacial operation and the benefit of integrated nanostructures is confirmed.

Role of Ag Addition on the Microscopic Material Properties of (Ag,Cu)(In,Ga)Se2 Absorbers and Their Effects on Losses in the Open‐Circuit Voltage of Corresponding Devices

ABSTRACTAg alloying of Cu(In,Ga)Se2 (CIGSe) absorbers in thin‐film solar cells leads to improved crystallization of these absorber layers at lower substrate temperatures than for Ag‐free CIGSe thin films as well as to enhanced cation interdiffusion, resulting in reduced Ga/In gradients. However, the role of Ag in the microscopic structure–property relationships in the (Ag,Cu)(In,Ga)Se2 thin‐film solar cells as well as a correlation between the various microscopic properties of the polycrystalline ACIGSe absorber and open‐circuit voltage of the corresponding solar cell device has not been reported earlier. In the present work, we study the effect of Ag addition by analyzing the differences in the various bulk, grain‐boundary, optoelectronic, emission, and absorption‐edge properties of ACIGSe absorbers with that of a reference CIGSe absorber. By comparing thin‐film solar cells with similar band‐gap energies ranging from about 1.1 to about 1.2 eV, we were able to correlate the differences in their absorber material properties with the differences in the device performance of the corresponding solar cells. Various microscopic origins of open‐circuit voltage losses were identified, such as strong Ga/In gradients and local compositional variations within individual grains of ACIGSe layers, which are linked to absorption‐edge broadening, lateral fluctuations in luminescence‐energy distribution, and band tailing, thus contributing to radiative VOC losses. A correlation established between the effective electron lifetime, average grain size, and lifetime at the grain boundaries indicates that enhanced nonradiative recombination at grain boundaries is a major contributor to the overall VOC deficit in ACIGSe solar cells. Although the alloying with Ag has been effective in increasing the grain size and the effective electron lifetime, still, the Ga/In gradients and the grain‐boundary recombination in the ACIGSe absorbers must be reduced further to improve the solar‐cell performance.

Molecular characteristics of sea spray aerosols during aging with the participation of marine volatile organic compounds

Sea spray aerosols (SSAs) are one of the largest natural sources of aerosols globally, known to affect the earth's radiation budget and to play a pivotal role in air quality and climate. The physical and chemical properties of organic components in SSA change during long-distance atmospheric transport over the ocean. To characterize the evolution of organic components during the aging process of SSA, in this study, we use a flow reactor to simulate the oxidation processes of SSA produced by authentic seawater via OH radicals (in the presence of organic gases evaporated from seawater) and to present the molecular signatures of the nascent and aged SSA. We found, under our experimental conditions, that oxidation of headspace organic gases during aging leads to significant formation of new particles and changes in the chemical constituents of SSA. In the nascent and aged SSA samples, we retained 129 and 340 products, respectively. The formation of high O/C and low carbon-number products was observed during the aging process, corresponding to functionalization and fragmentation reactions. Moreover, the significant contributions of compounds containing multiple nitrogen atoms and sulfate groups were observed in aged SSA for the first time, which can be attributed to the accretion reaction driven by OH heterogeneous oxidation and the formation of organic sulfur compounds, respectively. These findings provide additional insights into the atmospheric transformation of organic components in marine aerosols, which is important for understanding the global carbon cycle.

ReaxFF simulations on the transformation pathway of nitrogen elements in the heavy tar under oxy-coal combustion

Heavy tar is a crucial intermediate product during coal combustion. To explore the transformation pathway of N atoms in heavy tar under oxy-coal combustion, a comprehensive molecular model of heavy tar with typical N-containing functional groups was constructed. Different temperatures and chemical equivalence ratios were set for the oxy-coal combustion. The ReaxFF was employed to study various products' distribution and molecular numbers. The reaction network among different precursors and NOx was extracted, and the NO to N2 conversion mechanism was summarized. The results indicated that, like char combustion, the proportion of heavy tar gradually declined, the proportion of light tar and organic gas first rose and then gradually declined, and the proportion of inorganic gas continuously rose during heavy tar combustion. As the temperature increased, the proportion of cyanide precursors decreased, while the proportion of amine precursors and NOx increased. The oxidation of N-containing intermediates became more intense as the O2 content rose, but this oxidation effect was inhibited, and the NOx generation was reduced as the O2 content further increased. NO could bond with NHi, HNO, CN, and activate NO, decomposing to produce N2O, and N2O reacted with H radical to produce N2.

Hybrid System of Polystyrene and Semiconductor for Organic Electronic Applications

While organic semiconductors hold significant promise for the development of flexible, lightweight electronic devices such as organic thin-film transistors (OTFTs), photodetectors, and gas sensors, their widespread application is often limited by intrinsic challenges. In this article, we first review these challenges in organic electronics, including low charge carrier mobility, susceptibility to environmental degradation, difficulties in achieving uniform film morphology and crystallinity, as well as issues related to poor interface quality, scalability, and reproducibility that further hinder their commercial viability. Next, we focus on reviewing the hybrid system comprising an organic semiconductor and polystyrene (PS) to address these challenges. By examining the interactions of PS as a polymer additive with several benchmark semiconductors such as pentacene, rubrene, 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS pentacene), 2,8-difluoro-5,11-bis(triethylsilylethynyl) anthradithiophene (diF-TES-ADT), and 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT), we showcase the versatility of PS in enhancing the crystallization, thin film morphology, phase segregation, and electrical performance of organic semiconductor devices. This review aims to highlight the potential of an organic semiconductor/PS hybrid system to overcome key challenges in organic electronics, thereby paving the way for the broader adoption of organic semiconductors in next-generation electronic devices.

Enhanced response and recovery performance of α-hexathiophene sensors for NO2 gas by dual heterogeneous interface

Organic semiconductor gas sensors of α-hexathiophene (α-6 T) films as active layers with dual heterogeneous interface layers of p-hexabiphenyl and pentacene films are prepared by continuous vacuum evaporation method. The enhanced properties of sensors are achieved by modulating the thickness of the α-6 T films. The sensitivity of 1373 %/ ppm and a theoretical low detection limit of 361 ppb are obtained. The sensors demonstrate fast response and recovery properties of 1.05 and 1.51 min for NO2 gas of 20 ppm. The improved performance is attributed to the continuity of the interface layers and high adsorption of island-like growth. This approach is effective to improve organic sensors by introducing dual heterogeneous interface and tuning the growth of active layers.

A Comprehensive Study on Electrospun Cholesteric Liquid Crystal Core Fibers for Detecting Volatile Organic Compounds

Encapsulation of the cholesteric liquid crystal (CLC) into the core of poly(vinylpyrrolidone) (PVP) microfibers is accomplished via coaxial electrospinning technology and is applied to detect volatile organic compounds (VOCs). The impacts of various process parameters on the morphology of CLC fibers are deeply explored. The periodic arrangement of CLC molecules within the fibers enables the reflection of specific wavelengths. Consequently, changes in the reflected color of the CLC fiber membrane allow for the measurement and analysis of targeted gas molecules. The dynamic response of CLC fibers upon exposure to organic vapor is observed by a polarizing optical microscope, and its gray scale is used to quantitatively analyze the changes of reflected light signals of CLC fibers. Furthermore, the study investigates the reaction time for the failure of CLC molecular planar alignment in the CLC fiber membrane when subjected to perturbations induced by organic gases. The CLC fiber sensor exhibits heightened sensitivity to gases characterized by greater polarity. In light of potential future advancements, it is suggested that the spun fibers imbued with responsive properties through the incorporation of a liquid crystal core exhibit promise as a next-generation sensor technology in textile form, well-suited for applications in wearable technology.

Dynamic evolution of particulate and gaseous emissions for typical residential coal combustion

Residential coal combustion still accounts for half of the heating energy consumption in many developing countries. The dynamic variation during the combustion process importantly determines the combustion facility design and appropriate air quality assessment, which was omitted in conventional studies. This study investigated the emissions of particulate and gaseous pollutants during the combustion process for typical coal types using online monitoring. During the first pyrolysis stage with temperature climbing, the organic aerosols (OA) and gases reached peak concentration. The second fierce combustion stage had the highest temperature and produced the highest cumulative emissions, particularly a substantial amount of black carbon for coals with higher volatile content. Using higher-quality coals will undoubtedly reduce PM emissions, by a factor of 10 from bituminous to anthracite coal. However, more ultrafine particles (d < 0.1 μm) from cleaner coal may pose additional health risks. Anthracite and honeycomb coal had approximately twice the energy content and emitted more CO2 per unit mass of fuel and had more persistent SO2 emissions throughout the burnout stage. The oxygenation of OA and organic gases remained increased during combustion, suggesting the pyrolysis products underwent oxidation before being emitted. The investigation of the coal combustion process suggests the importance of reducing volatiles to control PM emissions, but the potential negative synergistic effects between PM reduction and increased carbon emissions should also be considered.

Fulde-Ferrel-Larkin-Ovchinnikov phase in a one-dimensional Fermi gas with attractive interactions and transverse spin-orbit coupling

Fulde-Ferrel-Larkin-Ovchinnikov phase in a one-dimensional Fermi gas with attractive interactions and transverse spin-orbit coupling

Application of low‐molecular‐weight polyethylene glycol‐modified silica in natural rubber composites

AbstractSilica serves as the primary filler in the fabrication of eco‐friendly tires, and achieving an optimal dispersion of polar silica within the natural rubber matrix is crucial for crafting high‐performance rubber composites. In this study, biodegradable surfactants polyethylene glycol (PEG) with molecular weights of 200, 400, and 800 were employed to modify silica. The modified silica was characterized by Fourier‐transform infrared spectroscopy; PEG‐modified silica with different molecular weights was compounded with Si69, a conventional silane coupling agent, in the formulation. This aimed to reduce Si69 dosage and mitigate the emission of volatile organic gases, such as ethanol, generated during the silanization reaction between Si69 and silica. Experimental findings revealed that compared with natural rubber composites containing six parts of Si69, the addition of PEG‐modified silica enhanced filler dispersion in the composite while reducing Si69 dosage by three parts. This led to accelerated vulcanization rates, effectively decreased energy consumption during production, and significantly improved wet slip resistance, while maintaining optimal rolling resistance. Rubber composites prepared with PEG800‐modified silica exhibited a 10% increase in elongation at break, a 12% increase in tensile product coefficient, and a 19% enhancement in wet slip resistance.Highlights Silica is modified by polyethylene glycol with molecular weight of 200, 400, and 800. The amount of silane coupling agent and VOC emissions are reduced. The interfacial bonding between silica and rubber matrix is enhanced. The tensile product coefficient and wet slip resistance are improved by 12% and 19%.