Carbon Components Research Articles

Recycling of coal gasification fine ash as a cement cleaning substitute: Performance, microstructure, and sustainability assessment of blended cement

Coal gasification fine ash (CGFA) is a large amount of solid waste produced by the coal chemical industry and has a broad prospect of recycling in building materials. This paper aims to investigate the effect of CGFA on the flowability, rheological behavior, hydration properties, and sustainability of blended cement. CGFA contains mineral components similar to fly ash (FA) and has morphological and physical filling effects that promote the flow of cement pastes. However, water absorption by the residual carbon component in CGFA resulted in severe deterioration of the rheological properties and flowability of the paste. As levels of CGFA replacement increase, the blended cement shows a pattern of decreasing early hydration rate, reducing flowability, and a significant increase in dynamic yield stress. The characteristic hydration reaction peak indicating the transformation of ettringite (AFt) to kuzelite (AFm) was little observed in the mixed samples of CGFA and cement. This phenomenon is attributed to the low content of reactive minerals (mainly aluminates) in CGFA. The residual carbon in CGFA almost did not participate in the hydration reaction of the blended cement system. It also limited the accumulation of hydration products, significantly reducing the strength of the mortar. Considering multiple factors such as cost, carbon emission, embodied energy, and cement consumption, the combined sustainability assessment of the (15%CGFA + 15%FA) combination replacing cement is 14.5% higher than that of pure cement mortar. This study can provide theoretical and technical support for the sustainable development of the coal chemical industry and the construction industry.

The missing information of aliphatic-like & aromatic-like Unresolved Complex Mixtures (UCMs) in background oceanic atmosphere: occurrence, identification and deposition

Oceanic air samples (gas + particle phases) were collected over the Shanghai-Arctic background oceanic region during the Chinese Arctic Research expedition 2021. Full scan mode (semi-quantitative) and selective ion monitoring mode (quantitative) were used to analyze separately 72 polycyclic aromatic compounds (PACs) & C11–C35 n-Alkanes (n-Alks) and unresolved complex mixtures (UCMs, including aromatic-like and aliphatic-like compounds) in these samples. The concentration of ΣPACs in the gas-phase and particle-phase were 0.40–8.5 ng m−3 (2.4 ± 1.7 ng m−3) and 0.059–1.1 ng m−3 (0.21 ± 0.23 ng m−3), respectively. While Σn-Alks in the gas-phase and particle-phase were 2.2–80 ng m−3 (mean = 18 ± 24 ng m−3) and 2.2–20 ng m−3 (mean = 8.6 ± 5.0 ng m−3), respectively. The semi-quantitative result indicated that aromatic-like UCMs were 14–1400 times higher than those of ΣPACs in these two phases, while aliphatic-like UCMs were 1.2–25 times higher than those of Σn-Alks. Through three-dimensional identification of the one-dimensional GC-MS chromatogram (with the x-axis representing GC retention time, the y-axis representing m/z, and the z-axis representing peak intensity), we found that aromatic-like UCMs were primarily composed of phenanthrene & anthracene similar PACs, while aliphatic-like UCMs were predominated by long-chain alkanes. The source identification shows that oil-gas leakage was the dominant source of PACs, followed by petroleum & coal combustion and biomass combustion; n-Alks might be mainly originated from anthropogenic sources, while nature sources at high latitudes cannot be ignored as well. Aromatic-like UCMs had a decreasing latitude trend and the presence of 5–6 ring aromatic-like UCMs enclosed within organic aerosols could pose a significant ecological risk, particularly in high latitude regions. Net uptake of atmospheric carbon caused by dry deposition of aromatic-like & aliphatic-like UCMs varied significantly geographically with mid- and low-latitude seas. The non-polar and weakly polar substances were not the major components of organic carbon in oceanic air of high latitude areas.

Iron ore reduction using agricultural waste biochar with different carbon to oxygen ratios

BackgroundDuring iron production ferric oxide is reduced to iron, with carbon used as the reducing agent. Traditionally, coke was used as the carbon component, which became a crucial raw material in the iron and steel industry after the industrial revolution. However, coke is the most significant contributor to CO2 emissions due to the source of heat and reducing agent. Thus, shifting to low carbon energy systems, such as those based on biomass, is challenging. Therefore, in this study, we employed the mushroom cultivation residue char (MCRC) as a reducing agent to investigate the feasibility of replacing coke in the production of metallic iron. MethodsAfter carbonization at different temperatures (500 °C, 700 °C and 900 °C), mushroom cultivation residue char (MCRC), were used as a reducing agent in the production of metallic iron. To create the composite pellets, the MCRCs were individually mixed with iron ore at different carbon to oxygen ratios (C/O) (0.7, 0.8 and 0.9) and 1 % of bentonite. The reduction process was undergoing in the electric muffle furnace at different high temperatures (1,000 °C, 1,200 °C and 1,300 °C) to investigate the biomass C/O ratios required for efficient iron production. Significant findingsThe results show that 0.8 was selected as the optimal C/O ratio for mushroom cultivation residue char (MCRC) to be used as a reducing agent. Its metallization rate can reach 31.99 %. The results also indicate that the carbon and volatiles in MCRC play a key role in iron making production using such biochar pellets. In conclusion, MCRC can be used as a reducing agent to increase the sustainability of iron production and reduce agricultural waste.

Assessment of light-absorbing carbonaceous aerosol origins and properties at the ATOLL site in northern France

Abstract. Understanding the lifecycle of light-absorbing carbonaceous aerosols, from emission to deposition, is critical for assessing their climate impact. This study integrated multi-year aerosol observations from the ATOLL (ATmospheric Observations in liLLe, northern France) platform, with air mass back trajectories and emission inventory as a newly developed “INTERPLAY” (IN-siTu obsERvations, hysPLit, And emission inventorY) approach. Applied to black carbon (BC), the method apportioned source contributions (shipping, vehicular, residential heating, industrial) and studied aerosol aging effects, notably on the brown carbon (BrC) component. Results estimate that, throughout the year, vehicular traffic dominated BC (31 %), followed by shipping (25 %, of which one-third was from canals/rivers) and residential heating (21 %). Comparing INTERPLAY results with the aethalometer model highlights that the “residential sector” BC can be entirely apportioned to BC from wood burning (BCwb), notably in winter, while vehicular traffic corresponds to only about 41 % of BC fossil fuel (BCff) at the ATOLL site, the rest being apportioned to shipping (33 %) and industrial (23 %) emissions. Thus, vehicular traffic and BCff should not be used interchangeably, particularly in regions near intense maritime traffic. Concerning BrC, our analysis confirms a dominant role of residential heating. Focusing on winter, results suggest a considerable decrease in the BrC component only 24 h after emission, with fresh residential emissions being responsible for 72 % of BrC absorption at ATOLL. The results from this study allow for an improved understanding of sources and atmospheric dynamics of light-absorbing carbonaceous aerosols in northern France, being crucial for both source abatement strategies as well as a better assessment of their climate impact.

Effect of auxiliary materials on the formation of humic acid carbon and nitrogen and bacterial dynamics in kitchen waste composting

This study investigated the impacts of different types of auxiliary materials on the humification process and bacterial dynamics during kitchen waste composting. Five types of auxiliary materials, including sawdust (SD), garden waste (GW), aquatic plants (AP), rice straw (RS), and rice husk (RH), were compared. The relationship between humic acid carbon and nitrogen components as well as bacterial community was analyzed by structural equation model and redundancy analysis. The results dindicated that SD and RS exhibited better thermophilic stage duration, germination index, and organic fractions degradation than other groups, which had higher degree of polymerization and the humification index of kitchen waste composting. AP, SD and RS had higher total nitrogen (TN) content and ammonia nitrogen accumulation, and RS had more humic acid nitrogen in TN with more amino acids and polyphenols precursors compared to other groups. High-throughput sequencing indicated that sawdust affected the variation of community structure and bacterial genera associated with lignocellulose degradation more than others. Redundancy analysis showed that Pseudoxanthomonas helped to the NH4+-N conversion to humic acid nitrogen for TN preservation. Structural equation modelling suggested that the conversion and utilization efficiency of microbes directly influenced the accumulation of humic acid carbon and nitrogen based on the types of intermediate metabolites. This study highlighted the role of auxiliary materials on improving the humification process of rapid kitchen waste composting.

Adsorption characteristics of coal gasification fine slag with alkali-dissolution and hydrothermal treatment on methylene blue

ABSTRACT The resource utilization of coal gasification fine slag (FS) and the harmless treatment of dyeing wastewater are crucial for establishing a zero-emission industrial system and a circular economy. This study used FS as raw material and divided it into two particle sizes through ultrasonic pretreatment enhanced wet sieving. The composite materials were synthesized via an alkaline hydrothermal process from different components in FS was compared, and applied as adsorbents for the removal of methylene blue from printing and dyeing wastewater. Finally, the kinetic and thermodynamic model developed for MB from printing and dyeing wastewater. The maximum adsorption of MB by the composite material prepared from low carbon component (<0.125 mm) could reach more than 180 mg·g−1. The research results have important theoretical and practical value for guiding the high-value utilization of FS and its application in dye wastewater treatment.

Source rock assessment and organic matter characterization of the Oligocene upper Shahejie and Dongying formations in the Nanpu depression of the saline lacustrine Bohai Bay basin, China: Geochemical, palynological, and mineralogical perspectives

The Bohai Bay Basin, located in eastern China, is a significant petroliferous, non-marine rift basin, underwent intricate tectonic activities throughout the Cenozoic. The Nanpu Depression in the Huanghua sub-basin in the northern part of the basin was controlled by Paleogene rifting and increased subsidence. These geological processes resulted in the deposition of the Shahejie and Dongying formations, which exhibited varying quantities and qualities of organic matter. Eighty drill cuttings samples of the Paleogene First Member (Es1) and the overlying Third (Ed3) and Second (Ed2) members of the Shahejie and Dongying formations, respectively, were investigated. An integrated approach including organic and inorganic geochemistry, palynology, and mineralogy was employed to assess the paleoredox and marine incursion conditions, source rock quality and levels of thermal maturity, and factors that governed organic matter accumulation. Results indicated that the Es1 Member was deposited under anoxic conditions, resulting in the accumulation of organic matter-rich mudstones in the Nanpu Depression. Abundant pollen grains and acritarchs were found in the Es1 Member yielded along with minor occurrences of dinoflagellate cysts, freshwater algae, and spores. Terrestrial palynomorph composition provided evidence of increased terrestrial runoff, while the high abundance of acritarchs, accompanied by some dinoflagellate cysts, confirmed episodes of marine incursion and deposition under hypersaline conditions in the lacustrine Bohai Bay Basin. The Ed2 Member exhibited poor to fair amounts of organic matter and a limited potential of hydrocarbon generation with a variety of kerogen Types, including IV, III, II/III, and II. The Ed3 Member shows fair to good organic matter richness and hydrocarbon potential of kerogen Types III, II/III, and II. The Es1 Member emerged as the most promising source rock within the studied interval, boasting good to excellent organic matter richness, and fair to good hydrocarbon generation potential of kerogen Types III and II/III. Evaluating the thermal maturity of organic matter, based on Tmax and VRo-Eq% and related cross-plots, revealed that the Shahejie and Dongying formations are still in the immature to the early stage of the oil window. The mineralogical composition of the Es1 Member primarily consists of clay and quartz with some carbonate and accessory minerals, such as epigenetic halite, dolomite, and plagioclase. Weak correlations observed between the total organic carbon (TOC) and mineral components indicated that the availability of organic matter was primarily controlled by enhanced production and preservation rather than limited dilution under saline lacustrine, oxygen-deprived, and well-stratified water column conditions. Regional investigations of the Es1 Member confirmed the widespread anoxia and deposition of organic-rich source rocks in the Bohai Bay Basin during the Oligocene.

Characterizing leaf-deposited particles: Single-particle mass spectral analysis and comparison with naturally fallen particles

The size and composition of particulate matter (PM) are pivotal in determining its adverse health effects. It is important to understand PM's retention by plants to facilitate its atmospheric removal. However, the distinctions between the size and composition of naturally fallen PM (NFPM) and leaf-deposited PM (LDPM) are not well-documented. Here we utilize a single-particle aerosol mass spectrometer, coupled with a PM resuspension chamber, to analyze these differences. We find that LDPM particles are 6.8–97.3% larger than NFPM. Employing a neural network algorithm based on adaptive resonance theory, we have identified distinct compositional profiles: NFPM predominantly consists of organic carbon (OC; 31.2%) and potassium-rich components (19.1%), whereas LDPM are largely composed of crustal species (53.9–60.6%). Interestingly, coniferous species retain higher OC content (11.5–13.7%) compared to broad-leaved species (0.5–1.2%), while the levoglucosan content exhibit an opposite trend. Our study highlights the active role of tree leaves in modifying PM composition beyond mere passive capture, advocating for a strategic approach to species selection in urban greening initiatives to enhance PM mitigation. These insights provide guidance for urban planners and environmentalists in implementing nature-based solutions to improve urban air quality.

Changes in soil organic carbon components and microbial community following spent mushroom substrate application.

While spent mushroom substrate (SMS) has shown promise in increasing soil organic carbon (SOC) and improving soil quality, research on the interplay between SOC components and microbial community following the application of diverse SMS types remains scant. A laboratory soil incubation experiment was conducted with application of two types of SMSs from cultivation of Pleurotus eryngii (PE) and Agaricus bisporus (AB), each at three application rates (3, 5.5, and 8%). Advanced techniques, including solid-state 13C nuclear magnetic resonance (NMR) and high-throughput sequencing, were employed to investigate on SOC fractions and chemical structure, microbial community composition and functionality. Compared to SMS-AB, SMS-PE application increased the relative abundances of carbohydrate carbon and O-alkyl C in SOC. In addition, SMS-PE application increased the relative abundance of the bacterial phylum Proteobacteria and those of the fungal phyla Basidiomycota and Ascomycota. The relative abundances of cellulose-degrading bacterial (e.g., Flavisolibacter and Agromyces) and fungal genera (e.g., Myceliophthora, Thermomyces, and Conocybe) were increased as well. The application of SMS-AB increased the aromaticity index of SOC, the relative abundance of aromatic C, and the contents of humic acid and heavy fraction organic carbon. In addition, SMS-AB application significantly increased the relative abundances of the bacterial phyla Firmicutes and Actinobacteria. Notably, the genera Actinomadura, Ilumatobacter, and Bacillus, which were positively correlated with humic acid, experienced an increase in relative abundance. Functional prediction revealed that SMS-PE application elevated carbohydrate metabolism and reduced the prevalence of fungal pathogens, particularly Fusarium. The application of high-rate SMS-AB (8%) enhanced bacterial amino acid metabolism and the relative abundances of plant pathogenic fungi. Our research provides strategies for utilizing SMS to enrich soil organic carbon and fortify soil health, facilitating the achievement of sustainable soil management.

The extraction of carbonate components from soils and sediments: an experimental investigation by using different leaching acids

The extraction of carbonate components from soils and sediments: an experimental investigation by using different leaching acids

Litter decomposition rate response to multiple global change factors: A meta-analysis

Anthropogenic global change fundamentally impacts ecosystem biogeochemical cycling. Although litter decomposition is a crucial component of carbon (C) cycling, its response to diverse global change factors (GCFs) remains uncertain. In this research, we synthesized 1706 observations from 260 peer-reviewed publications to elucidate the effects of GCFs on litter decomposition rate (k) and the contribution of different variables to them. Overall, nitrogen (N) addition and drought significantly decreased k (−3.3 and −17.7%, respectively), phosphorus (P) addition, warming, and increased precipitation significantly increased k (6.7, 8.2, and 11.6%, respectively), while elevated CO2 had an insignificant effect on k (−0.6%). Combined GCFs had no significant effect on k except for warming*drought, and all combined factors mainly exhibited antagonistic interactions. Further analysis showed that k responses to GCFs were influenced by initial litter quality (C, N, C:N, P, cellulose, lignin, and vegetation types), soil properties (soil organic C, soil total N, soil total P, soil respiration and microbial biomass C), environmental factors (latitude, longitude, annual mean temperature, annual mean precipitation, ecosystem type, and climate type), and experimental methods (experiment type, richness, treatment method, fertilizer form, fertilizer rate, and experimental duration). Initial litter quality predominantly governed the k response to N addition (53.5%), while soil properties were more significant in regulating the P addition response (44.8%). Environmental factors largely determined k responses to warming, drought, and increased precipitation (50.6, 54.7, 46.9%). Moreover, the experimental methodology also played an important role in regulating k responses to GCFs, which explained 8.6, 23.6, 31.1, 23.7, and 29.7% of the variation of the responses of k to N addition, P addition, warming, drought, and increased precipitation. This meta-analysis offers improved global-scale nutrient cycling predictions under climate change and underscores the need for long-term, multi-factor, methodologically standardized experiments to accurately predict the influence of GCFs on litter decomposition.

Phosphorus addition enhances heterotrophic respiration but reduces root respiration in a subtropical plantation forest

Soil respiration (Rs) is a major component of the global carbon (C) cycle and is influenced by the availability of nutrients such as phosphorus (P). However, the response of Rs to P addition in P-limited subtropical forest ecosystems and the underlying mechanisms remain poorly understood. To address this, we conducted a P addition experiment (50 kg P ha−1 yr−1) in a subtropical Chinese fir (Cunninghamia lanceolata) plantation forest. We separated Rs into heterotrophic respiration (Rh), root respiration (Rr), and mycorrhizal hyphal respiration (Rm), and quantified soil properties, microbial biomass (phospholipid fatty acid, PLFA), fungal community composition (ITS), and the activity of extracellular enzymes. Phosphorus addition significantly increased Rs and Rh, but decreased Rr and did not influence Rm. Further, P addition increased fungal, bacterial, and total PLFAs, and phenol oxidase activity. Conversely, P application decreased root biomass and did not alter the relative abundance of symbiotrophic fungi. Phosphorus enrichment therefore enhances soil C emissions by promoting organic matter decomposition by heterotrophic activity, rather than via increases in root or mycorrhizal respiration. This advances our mechanistic understanding of the relationship between fertility and soil respiration in subtropical forests, with implications for predicting soil C emissions under global change.

Microbial transformation mechanisms of particulate organic carbon to mineral-associated organic carbon at the chemical molecular level: Highlighting the effects of ambient temperature and soil moisture

Soil dissolved organic matter (DOM), an important component of active soil organic carbon (C), plays a crucial role in controlling C transformation. However, the role of DOM in mediating the conversion of particulate organic C (POC) into mineral-associated organic C (MAOC) at the molecular level remains unclear. In this study, the microbial conversion of POC to MAOC at the molecular level was investigated at different ambient temperatures and soil moisture levels. An increase in ambient temperature led to the conversion of POC to labile C, whereas MAOC increased with soil moisture. CHO, CHNO, and CHOS increased with soil moisture and temperature. The highest temperature (35 °C) promoted conversion of lignin/cram (carboxyl-rich alicyclic molecules)-like molecules into aromatic components with the highest intragroup transformation of DOM (74%). The highest soil moisture (60%) favoured the conversion of refractory substances into aliphatic/peptide and lipid components with the highest intergroup transformation (28%). Compared to fungi, bacteria were the main driving force for DOM transformation. Therefore, changes in ambient temperature and soil moisture control the microbial formation and transformation of different C fractions (i.e. POC and MAOC) via DOM differently at the molecular level.

Reducing carbon emissions in prefabricated buildings supply chains: a focus on component manufacturing processes.

The construction sector accounts for 23% of emissions from global economic activity, with China responsible for nearly 41%. Although China has vigorously promoted the development of prefabricated buildings (PBS) in pursuit of cleaner production, the carbon emissions from prefabricated component factories (PCF) should not be underestimated. So, the focus of this research was on how to promote the decarbonization of PCF. Based on the carbon trading market mechanism, the carbon emissions trading tax and revenue tax collection, the authors established a differential game model consisting of the local government and the PCF, studied the equilibrium solutions under different decision models, and analyzed the roles of the two tax systems, carbon trading revenue, and market preferences. The results are as follows: (1) The PCF's low-carbon technology (LCT) innovation efforts can be directly affected by the carbon price, component price, and tax rate and indirectly affected by influencing the local government's efforts. Besides, the local government and the PCF strategies can be changed through the central government's regulation of carbon prices and tax rates. (2) PCF should set reasonable prices for components, improving economic efficiency and the LCT stocks. (3) Cost-sharing contracts can encourage PCF to increase their LCT innovation, which is conducive to increasing the optimal benefits of the PCF. (4) The local government cannot be motivated by cost-sharing contracts. They can increase their optimal benefits only if the cost-sharing coefficient is below a threshold or if the environmental benefits from low-carbon production are above a specific value.

The inputs of autochthonous organic carbon driven by mangroves reduce metal mobility and bioavailability in intertidal regions

The significance of mangroves in carbon storage is widely acknowledged. However, the potential role of carbon enhancement driven by mangroves in mitigating the risk of metal exposure remains unclear. In this study, a natural mangrove reserve located in Futian was selected to investigate the potential role of autochthonous organic carbon on metal bioavailability. The presence of mangroves seemed to have little effect on the accumulations of Cu(II), Zn(II), Cr(VI/III), Pb(II), and Ni(II) in surface sediments. Metal mobility and bioavailability, however, were found to be directly influenced by the presence of mangroves. Compared with mudflat, mangrove sediments exhibited an obvious in the bioavailability of Cu(II), Zn(II), Cr(VI/III), Pb(II), and Ni(II) by 19–79 %, with the highest reduction occurring in the interior of mangroves dominated by K. obovata. Mangroves also significantly enhanced the accumulation of organic carbon in sediments, regardless of carbon components. Moreover, the results from random forest analysis further showed that autochthonous organic carbon was the most important carbon component that negatively related to metal bioavailability. In summary, this is the first study to provide a linkage between mangrove cover and increased autochthonous organic carbon input, which decreases metal bioavailability. The present data also suggest that mangroves are an efficient natural barrier to alleviate the risk of metal exposure in intertidal regions.

Investigating the effects of silicon and carbon components on the thickness evolution and performance degradation of silicon–carbon electrodes through electrochemical dilatometry

The severe volumetric changes occur during the lithiation/de-lithiation of silicon materials, which are the main cause of battery capacity failure. In this study, the expansion behavior of a cell composed of a silicon-carbon anode and Li(Ni0.5Co0.2Mn0.3)O2 (NCM523) was measured using the electrochemical dilatometry, and the contributions of different silicon and carbon components to the expansion were analyzed, along with factors affecting the cyclic stability of the silicon carbon anode. The results indicate that amorphous carbon can inhibit the volume expansion of monocrystalline silicon in the late stage of lithiation, thereby ensuring the cyclic stability of silicon. The cyclic stability of silicon-carbon composites is affected by irreversible expansion and expansion variation, and these two factors are negatively correlated. This research provides insights and guidance for the design of silicon carbon electrodes with superior electrochemical performance.

Seasonal variations and sources of atmospheric EPFRs in a megacity in severe cold region: Implications for the influence of strong coal and biomass combustion

Environmentally persistent free radicals (EPFRs) can pose exposure risks by inducing the generation of reactive oxygen species. As a new class of pollutants, EPFRs have been frequently detected in atmospheric particulate matters. In this study, the seasonal variations and sources of EPFRs in a severe cold region in Northeastern China were comprehensively investigated, especially for the high pollution events. The geomean concentration of EPFRs in the total suspended particle was 6.58 × 1013 spins/m3 and the mean level in winter was one order of magnitude higher than summer and autumn. The correlation network analysis showed that EPFRs had significantly positive correlation with carbon component, K+ and PAHs, indicating that EPFRs were primarily emitted from combustion and pyrolysis process. The source appointment by the Positive Matrix Factorization (PMF) model indicated that the dominant sources in the heating season were coal combustion (48.4%), vehicle emission (23.1%) and biomass burning (19.4%), while the top three sources in the non-heating season were others (41.4%), coal combustion (23.7%) and vehicle emissions (21.2%). It was found that the high EPFRs in cold season can be ascribed to the extensive use of fossil fuel for heating demand; while the high EPFRs occurred in early spring were caused by the large-scale opening combustion of biomass. In summary, this study provided important basic information for better understanding the pollution characteristics of EPFRs, which suggested that the implementation of energy transformation and straw utilization was benefit for the control of EPFRs in severe cold region.

Recent Advances in the Development of Nanocarbon-Based Electrocatalytic/Electrode Materials for Proton Exchange Membrane Fuel Cells: A Review

The global issue for proton exchange membrane fuel cell market development is a reduction in the device cost through an increase in efficiency of the oxygen reduction reaction occurring at the cathode and an extension of the service life of the electrochemical device. Losses in the fuel cell performance are due to various degradation mechanisms in the catalytic layers taking place under conditions of high electric potential, temperature, and humidity. This review is devoted to recent advances in the field of increasing the efficiency and durability of electrocatalysts and other electrode materials by introducing structured carbon components into their composition. The main synthesis methods, physicochemical and electrochemical properties of materials, and performance of devices on their basis are presented. The main correlations between the composition and properties of structured carbon electrode materials, which can provide successful solutions to the highlighted issues, are revealed.

Soil column-experimental research on the migration pattern of petroleum pollutant in the soil

In the process of oilfield exploitation and production, harmful pollutants, such as Crude oil that falls to the ground (generally refers to crude oil that leaks to the ground during oil production or transportation), production wastewater and oil-bearing mud are produced. In this contribution, the soil and crude oil from Daqing area are adopted as experimental materials to make a soil column-experimental device. The results show that the maximum migration depth of petroleum pollutants is 25 cm, most of the pollutants exist above 10 cm. The components of pollutants in disturbed soil column are complex, and the peak area of each component is large, mainly distributed in C12–C28, while in undisturbed soil column, the content of pollutants is small, and the peak area of each component is also small, mainly distributed in C12–C22. With the increase of depth, the relative content of aromatic hydrocarbons increases. The migration ability of low carbon component is weaker than the other components in crude oil. The components with high carbon number are significantly higher in shallow part. The relative contents of each component from high to low are saturates, aromatic hydrocarbons, resin and asphaltene in the soil. Compared with disturbed soil columns, the structure of undisturbed soil is complex, and the migration rate of pollutants in undisturbed soil is slower than that in disturbed soil. With the increase of depth, the light components of disturbed soil columns gradually decrease, and the relative content of heavy components changes little. The light components of the undisturbed soil column also gradually decreased, and the heavy components greater than C22 did not migrate to the depth of the soil column.

Dielectric-magnetic synergistic construction of 2D FeCo/Co8FeS8/C composites for efficient electromagnetic wave capture

Nowadays, the issue of electromagnetic pollution has become increasingly prominent, underscoring the critical importance of developing high-performance microwave absorbers. This study put forwards the synthesis process of two-dimensional (2D) FeCo/Co8FeS8/C carbon nanosheets, wherein CoSO4 and FeCl3 serve as inorganic salt templates, and dopamine functions as the carbon source. FeCo alloy nanoparticles and Co8FeS8 nanoparticles are loaded on the surface of the carbon layer. 2D structure forms the conductive network, which proves advantages in establishing efficient electronic channels and minimizing conduction losses. The carbon component increases the dielectric constant of the composite and improves its impedance matching, and the FeCo alloy provides a certain ML. The synergistic effect between these components significantly contributes to the exceptional microwave absorption performance of the composites. Accordingly, the minimum reflection loss (RLmin) of FeCo/Co8FeS8/C composite reaches −47.4 dB, its effective absorption bandwidth (EAB) reaches 5.3 GHz. In particular, CST confirms that radar cross-section reduction value of FeCo/Co8FeS8/C composite can reach 20.2 dB m2 in the range of −90° < phi< 90°, indicating a high microwave attenuation ability. The study introduces a novel strategy for advancing the development of two-dimensional carbon-based absorption materials.