Residual Carbon Research Articles

Longitudinal modeling of residual carbon dioxide and residual feed intake in the Nordic Red dairy cattle

Feed utilization efficiency is an important trait in dairy production playing a significant role in reducing feed costs and lowering methane emission. One of the metrics used to measure feed efficiency in dairy cows is residual feed intake (RFI). This metric requires routine measurement of feed intake. Since there is a positive high correlation between heat production and carbon dioxide (CO2) production on the one hand and heat production and efficiency on the other hand, residual carbon dioxide (RCO2) might be a useful metric to improve feed efficiency. The objectives of this study were to model the trajectories of RCO2 and RFI as well as to estimate their repeatabilities and correlations at different stages of lactation. Daily CO2 output and feed intake were recorded from 46 primiparous Nordic Red dairy cows using two Greenfeed Emissions Monitoring™ systems from 2 to 305 days in milk (DIM). Edited data comprised 5 995 daily averages. To calculate predicted values of CO2 and DM intake (DMI), prediction models were developed by fitting multiple regression models to observations. Subsequently, RCO2 and RFI were calculated by subtracting predicted values of CO2 and DMI from their corresponding actual observations. A random regression bivariate model was fitted to estimate repeatabilities and animal correlations within lactation at different DIMs between RCO2 and RFI traits. The model fitted included fixed effects of year-month of recording, lactation month, fixed regressions as well as random regressions for the animal effect. The residual variance was considered to be heterogeneous. Repeatabilities and animal correlations of RCO2 and RFI between selected DIM (for every 30 DIM i.e., 6, 36,…, 246 and 276) were calculated. Repeatability of RCO2 was high at the beginning of lactation (0.72 at DIM 6) and decreased around the peak of milk production (0.27 at DIM 96) and again increased gradually toward the end of lactation. Similarly, RFI also had high repeatability at the beginning (0.86 at DIM 6); however, it decreased in mid-lactation (0.37 at DIM 156) and then increased toward the end of lactation. Animal correlations between RCO2 and RFI were moderate to high on the same DIM and ranged from 0.37 to 0.88. Overall, we found that animals with higher CO2 production than expected also consume more DMI than expected, but the moderate correlation between RCO2 and RFI found in this study calls for more research to assess the potential of RCO2 to become a new feed efficiency metric.

VARIABLE SELECTION METHODS APPLIED IN HTGC DATA TO DETERMINE PHYSICOCHEMICAL PROPERTIES OF CRUDE OILS

High-temperature gas chromatography (HTGC) is an analytical technique employed in the petroleum industry for component separation. By incorporating chemometrics, HTGC data can be effectively utilized to predict various properties of crude oil. However, HTGC chromatograms generate a substantial number of variables, some of which may lack pertinent chemical information. Consequently, employing variable selection methods becomes crucial to reduce the number of variables and enhance the predictive capability of calibration models. In this study, the interval partial least squares (iPLS), synergy interval partial least squares (siPLS), and ordered predictors selection (OPS) methods were applied for variable selection to construct linear regression models. The main objective was to investigate the potential of these methods in predicting eight properties of crude oil: American Petroleum Institute (API) gravity, standardized kinematic viscosity at 50 °C (VISp), flash point (FP), Reid vapor pressure (RVP), micro carbon residue (MCR), saturates (SAT), aromatics (ARO), and polar (POL) content. While all variable selection methods yielded satisfactory results, the OPS-PLS regression models consistently exhibited the best performance in estimating these properties, achieving root mean squared error of prediction (RMSEP) values of 1.244 for API, 0.029 for VISp, 15.356 °C for FP, 0.324 kPa for RVP, 0.629 wt% for MCR, 3.691 wt% for SAT, 2.939 wt% for ARO, and 3.374 wt% for POL. Variable selection demonstrated remarkable effectiveness, significantly improving the accuracy of the models, and allowing for the creation of concise models with a focused set of variables.

Assessing groundwater quality in Nand Samand catchment, Rajasthan, India: a GIS-based multi indices approach for drinking and irrigation water suitability

Abstract Consistently monitoring groundwater quality (GWQ) is essential to reduce the risk of geochemical contaminants and ensure its suitability for agriculture and human consumption. The current investigation aims to assess groundwater (GW) acceptability in the Nand Samand catchment (NSC), utilizing the water quality index (WQI) and irrigation water quality indices (IWQIs) for domestic and irrigation purposes. To achieve this, GW samples were collected from 95 open wells which were located spatially in the catchment, during the pre-monsoon (PRM) and post-monsoon (POM) seasons of 2019 and 2020, and subsequently analysed for 11 physico-chemical parameters. Electrical conductivity (EC) varied from 1.25 to 6.61 dS/m and 0.58 to 7.42 dS/m during the PRM and POM seasons, respectively. Total dissolved solids of the study area ranged between 180 and 1,180 (27%) to 1,180 and 2,180 (62%) during PRM 1,180 (63%) to 1,180–2,180 (31%) during POM, respectively. The study also computed the ‘sodium adsorption ratio’ (SAR) and ‘residual sodium carbonate’ (RSC) to estimate GW's appropriateness for agriculture, finding it suitable in most locations due to its balanced composition. Based on WQI, varying percentages of samples were classified as ‘good’ and ‘poor’ for potable water quality in both seasons.

Effect of graphene oxide and carbon black on the thermoelectric performance of niobium doped strontium titanate

Strontium titanate-based ceramics are promising n-type thermoelectrics due to their low cost and high thermal and chemical stability. Here, SrTi0.85Nb0.15O3 was prepared with carbon additions of electrochemically produced graphene oxide (eGO) and commercially available carbon black (CB). Ceramic samples were sintered at 1700 K under a reducing atmosphere. XRD, HR-TEM and Raman spectra confirmed the matrix phase was cubic perovskite; there were no carbon residues. By incorporating graphene oxide, the electrical conductivity increased nine-fold to 2818 S cm−1 at 300 K as a result of enhanced carrier mobility. In contrast, the carbon black samples exhibited low density and a small average grain size of ∼1 μm. High-resolution X-ray photoelectron spectroscopy revealed the presence of a large number of ionised impurities in the carbon black samples, which significantly enhanced scattering effects; low thermal conductivities of 1.7 W m−1 K−1 were achieved at 873 K. The work reveals that eGO promotes charge transport in SrTiO3, while CB significantly suppresses phonon transport. Both effects are relevant to the development of other thermoelectrics.

Downsizing and coating effects on the electrochemical performance of Mn-doped iron fluorophosphate as cathode material for sodium-ion batteries

Sodium Mn-doped iron fluorophosphate Na2Fe0·5Mn0·5PO4F is a potential positive electrode material for lithium-ion and sodium-ion batteries. This study outlines the synthesis of Na2Fe0·5Mn0·5PO4F powder through a simplified and more accessible production method. The X-rays diffraction (XRD) technique showed a pure phase with monoclinic symmetry (S.G. P21/n). The resulting uncoated material (labeled as NFeMPF) was ball-milled with dopamine hydrochloride (mentioned as dopamine hereafter) as a carbon source to enhance the specific surface and improve its electronic conductivity. Raman spectra confirmed the presence of residual carbon after the pyrolysis process. Thermogravimetric analysis (TGA) demonstrated the stability of Mn-doped iron fluorophosphate up to 1000 °C. Additionally, Mössbauer spectroscopy disclosed structural improvements in the material, indicating the reduction of all Fe(III) when coated with dopamine. The uncoated material discharge capacity when cycled against sodium exhibits reversible capacities of only 80, 67, and 38 mAh/g during the first cycle at C/20, C/16, and C/5, respectively. The coated NFeMPF@D delivered improved capacities of 272 and 202 mAh/g at C/20 and C/16, respectively. This highlights the considerable promise of the investigated phosphate-based electrode material as a cathode composite for the next generation of sodium-ion batteries.

Spatial distribution and hydrogeochemical evaluations of groundwater and its suitability for drinking and irrigation purposes in kaligonj upazila of satkhira district of Bangladesh

Groundwater is a significant water resource for drinking and irrigation in Satkhira district, Bangladesh. The depletion of groundwater resources and deterioration in its quality are the results of the confluence of factors such as industrialization, intensive irrigation, and rapid population growth. For this reason, this study focused on the evaluation of tubewell water of six unions of Kaligonj upazila in Satkhira district, which is situated in the coastal southwest part of Bangladesh. Major and trace elemental concentrations were assimilated into positive matrix factorization (PMF) to identify potential sources and their respective contributions. Principal component analysis (PCA) revealed that groundwater salinization and manmade activities were the primary causes of heavy metals in the coastal groundwater. Its average pH value was found to be 7.5, while Dissolved oxygen, Total dissolved solids, salinity, and conductivity, with values ranging from 1.18 to 7.38 mg/L, 0.5–4.88 g/L, 0.4–5%, and 0.95 to 8.56 mS/cm, respectively. The total hardness average value was 561.7 mg/L, classified into the very hard water categories, which is why 90% of the tubewell water samples were unfit for household purposes. All samples had an excessive level of arsenic present. The iron concentration of fifteen (15) samples crossed the standard limit according to WHO 2011 value. Around 63% of the samples were of the Na+-K+-Cl--SO42- type, and about 72% were sodium-potassium and alkali types. 98% of samples were covered in chloride and bicarbonate. The findings showed that 45.83% of the groundwater samples had negative Chloroalkaline index (CAIs), while 54.16% had positive. The permeability index (PI) was an average of 73%, and residual sodium carbonate (RSC) averaged 260.2 mg/L, and the findings clearly showed that 80% of the samples weren't appropriate for irrigation. According to the sodium adsorption ratio (SAR) value, 65% of the samples fell into the unsuitable category. These calculations indicated a high overall salinity hazard in the study area, which may be caused by the intrusion of sea water given that the study area is close to the coastal region. Findings compared to standards revealed that the majority of the samples were deemed unfit for drinking and irrigation purposes. Hence, additional attention must be paid to this area to ensure the availability of drinkable water and to preserve sustainable farming practices.

Design and preparation of sulfur vulcanized polyamide 66 cross-linked nitrile butadiene rubber networked and its application in blending with graphene oxide

This study investigates the effect of a multiphase crosslinked network structure formed using a sulfur vulcanization system on the vulcanization, thermal stability, and mechanical and tribological properties of nitrile butadiene rubber/polyamide 66/graphene oxide (NBR/PA66/GO) composites. Differential scanning calorimetry and glass transition temperature (Tg) were used to evaluate thermal stability. Samples doped with 1 phr of sulfur (1S) have the best "residual carbon at 800 °C" and Tg. The surface morphology after friction wear was characterized using scanning electron microscopy and a 3D profilometer. The tensile and tear strengths of 1S increased by approximately 74 % and 39 %, respectively, compared to those of 0.5S. The coefficient of friction was reduced by approximately 61 % compared to that of 3S. Molecular dynamics simulations were used to explore the microscopic mechanism underlying the effect of the crosslinked structure of the composites on their properties. The NBR/PA66/GO composite exhibited the best 1S properties. However, when the sulfur content was higher, excessive cross-linking occurred, and the sulfide cross-linking network structure inside the matrix was damaged. This study also provides a viable strategy for the preparation of vulcanized rubber-plastic blend composites with potential for a wide range of industrial applications.

Oxygen vacancy-promoter on flotation residue carbon from coal gasification fine slag for the catalytic degradation of phenol

To enable the high-value application of coal gasification slag, flotation residual carbon from coal gasification fine slag (FSC) was used as a catalyst to remove organic contaminants. In this study, residual carbon was washed and sieved to prepare a stable carbon-based catalyst, which was used to activate peroxymonosulfate (PMS) for phenol degradation. The findings demonstrated that 50 mg/L of phenol could be removed by the FSC in 30 minutes within 30 °C, pH 3.01–11.00, 1 mmol/L PMS, and 0.6 g/L catalyst dosage. The efficiency of phenol degradation was attributed to the abundant active sites, such as oxygen vacancies in FSC. The characterization results demonstrated that oxygen vacancies, as a defective structure, could promote the adsorption of PMS on the FSC surface, then forming various active species, such as ·O2- and 1O2. Moreover, the presence of oxygen vacancies could redistribute the charge on the FSC surface, thus improving the adsorption and degradation of phenol. Overall, the study confirmed the activation potential of the flotation residual carbon from coal gasification fine slag and provided a theoretical foundation for its application in the catalytic removal of organic pollutants.

Hydrothermal carbonization of Chinese medicine residues: Formation of humic acids and combustion performance of extracted hydrochar

Aiming at the sustainable management of high-moisture Chinese medicine residues (CMR), an alternative way integrating hydrothermal carbonization (HTC), humic acids (HAs) extraction and combustion of remained hydrochar has been proposed in this study. Effect of HTC temperature, HTC duration, and feedwater pH on the mass yield and properties of HAs was examined. The associated formation mechanism of HAs during HTC was proposed. The combustion performance of remained hydrochar after HAs extraction was evaluated. Results show that the positive correlation between hydrochar yield and HAs yield is observed. According to three-dimensional excitation emission matrix (3D EEM) fluorescence intensity, the best quality of HAs is achieved with a yield of 8.17 % at feedwater pH of 13 and HTC temperature of 200 °C. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses show abundant aromatic and aliphatic structure as well as oxygenated functional groups in HAs, which is like commercial HAs (HA-C). Besides, in terms of comprehensive combustion index (CCI), HTC can improve the combustion performance of CMR, while it becomes a bit worse after HAs extraction. Higher weighted mean apparent activation energy (Em) of hydrochar indicating its highly thermal stability. HAs extraction reduces Em and CCI of remained hydrochar. However, it can be regarded a potential renewable energy. This work confirms a more sustainable alternative way for CMR comprehensive utilization in near future.

Investigation of Water Quality of the Karasu River in Bilecik Province in terms of Agricultural Irrigation

Together with increasing people's need for water, water needs to be monitored due to the pressure created by factors such as drought and pollution. In this study, water quality was monitored by determining 10 points on the Karasu River in Bilecik Province and it was aimed to examine the seasonal change in water quality. pH, EC, Na, K, Ca, Mg, CO3, HCO3, Cl, B, SO4, Sodium Adsorption Rate (SAR), Residual Sodium Carbonate (RSC) and %Na parameters were determined in water. And then using these parameters, quality classes were determined with the help of water quality classification systems developed by scientists such as Schofield, Wilcox, Thorne, Doneen and Soifer. The study were temporally diveded into 4 periods. They are period 1, period 2 (Spring), period 3 (Summer) and period 4 (Fall). After all, for the period 3, heavy metal pollution, especially Al, attracts attention. Except for the period 2 of point 7 and period 4 of point 9, the class of all periods and points in terms of sulphate was "Very good (class 1)". According to Schofield (1933 and 1935) systems, point 7 is in particularly bad situation in terms of EC. According to Wilcox (1948), point 7 is not suitable for irrigation in the period 2. At point 7, water pollution in period 2 has been identified as common to most classification systems. According to Christiansen et al. (1977), there is intense pollution in terms of EC and Na2CO3 parameters. According to Soifer (1987), point 2 is the cleanest point. As a result, Karasu river is not suitable for irrigation in terms of Al and B. It was understood that heavy metal pollution did not cause much of a problem in non-industrialized cities such as Bilecik. Besides, it was understood that the most common element among heavy metals was Pb in Karasu River. The SAR and RSC values of all periods, seasons and points were classified as "Very Good-Safe (C1S1)".

Unravelling the main mechanism responsible for nocturnal CO2 uptake by dryland soils

Soil respiration, or CO2 efflux from soil, is a crucial component of the terrestrial carbon cycle in climate models. Contrastingly, many dryland soils absorb atmospheric CO2 at night, but the exact mechanisms driving this uptake are actively debated. Here we used a mechanistic model with heuristic approaches to unravel the underlying processes of the observed patterns of soil-atmosphere CO2 fluxes. We show that the temperature drop during nighttime is the main driver of CO2 uptake by increasing CO2 solubility and local water pH of a thin water film on soil particle surfaces, providing favourable conditions for carbonate precipitation. Our data demonstrate that the nocturnal inorganic carbon absorption is a common soil process, but often offset by biological CO2 production. The uptake rates can be impacted by different successional stages of biocrusts that consume or produce CO2 and modify the pH of the soil water film, which can be maintained by non-rainfall water inputs, such as pore space condensation. Annual estimates of nocturnal carbon uptake, based on in situ continuous measurements at the soil level in drylands are still very scarce, but fluxes of up to several tens of g C m−2 y−1 have been reported, potentially accounting for a considerable fraction of the global residual terrestrial carbon sink.

A novel co-continuous Si–Zr hybrid phenolic aerogel composite with excellent antioxidant ablation enabled by sea-island-like ceramic structure at high temperature

Lightweight phenolic matrix composites are highly potential in ablative thermal protective materials for future aerospace vehicles, and hybrid modification is considered as one of effective ways to improve the oxidation and ablation resistance of phenolic matrix. Herein, the co-continuous silica zirconium hybrid phenolic resin (SZRx) was synthesized, which can be used to prepare lightweight ablation resistant aerogel composites by the sol-gel method. The SZRx aerogel showed stable porous structure and excellent hydrophobicity, and the silicon zirconium hybrid greatly improved the high temperature carbon residue and oxidation resistance of phenolic resin. The SZRx aerogel composites also possessed excellent integrated characteristics of heat protection and insulation, with a linear ablation rate as low as 0.032 mm/s and a back temperature below 200 °C. The synergistic effect of silicon and zirconium formed the multiphase ceramic layer (C, SiO2, SiC and ZrO2) with the sea-island-like structure on the surface of the composite material, which can effectively resist high-temperature ablation and aerodynamic exfoliation. This can indicate that silicon zirconium dual element hybrid phenolic resin is the highly competitive matrix for lightweight and ablation resistant composite materials.

Functionalized lignin nanoparticles assembled with MXene reinforced polypropylene with favorable UV-aging resistance, electromagnetic shielding effects and superior fire-safety

Deterioration in mechanical performances and aging resistance due to the introduction of flame retardants is a major obstacle for bio-based fire-safety polypropylene (PP). Herein, we reported a kind of functionalized lignin nanoparticles assembled with MXene (MX@LNP), and applied it to construct the flame-retardant PP composites (PP-MA) with superior fire safety, excellent mechanical performance, electromagnetic shielding effects and aging resistance. Specifically, the PP-MA doped with only 18 wt% flame-retardant additives (PP-MA18) achieved the UL-94 V-0 rating. In comparison to pure PP, PP-MA18 presented a greatly decreased peak of heat release rate (pHRR), total heat rate (THR), and peak smoke production rate (pSPR) by 79.7 %, 69.0 % and 75.8 %, respectively, and satisfactory decrease in total flammable and toxic volatiles evolved. The formed fine solid microstructure of carbon residuals effectively promoted the compactness of char layers. More importantly, the nano-effect and the strong interface interaction between the complexed MX@LNP and PP enhanced the tensile strength (45.78 MPa) and elongation at break (725.95 %) of PP-MA. Additionally, the significant ultraviolet absorption and electromagnetic wave dissipation performance of MXene and lignin enabled excellent aging resistance and electromagnetic shielding effects of PP-MA compared with PP. This achieved MX@LNP afforded a novel approach for developing flame retardant materials with excellent application performance.

Heavy oil atmospheric residue: HDS performance and life test using ARDS catalysts system

The objective of this study is to evaluate the catalyst by introducing atmospheric residue of heavy crude (H-AR) that secures full comprehensive characteristics and converts into a petroleum product, namely low sulfur fuel oil (LSFO). Furthermore, to estimate the catalyst’s lifespan under hydroprocessing conditions by monitoring its deactivation rate and maintaining consistent sulfur in LSFO products through gradual increases in reaction temperature. Prior to the hydrotreating test, the heavy crude oil underwent desalting, dewatering, and atmospheric distillation to obtained atmospheric residue (H-AR, i.e., 350°C+) for use as feedstock. The pilot plant employed a catalyst system comprising both hydrodemetallization (HDM) and hydrodesulfurization (HDS) catalysts, distributed across two fixed-bed reactors. The results showed the lifespan approximately 3.0 months as a function of time-on-stream (TOS). The H-AR feed, with its high sulfur, metals, asphaltenes, and micro carbon residue (MCR) content, poses several challenges including carbon deposition at start of run (SOR). The observed deactivation rate is attributing to the feedstock’s poor quality and its impact associated deposition of coke and metals (V and Ni) deposition with TOS.

Properties of Thermoplastic High-ortho Phenolic Epoxy Fibers

The thermoplastic high-ortho phenolic resins (HPRs) were synthesized by a one-step synthesis using phenol, formaldehyde, zinc acetate, sulfuric acid, and small amounts of ethanol. It was then blended with epoxy resins, and a small amount of ethylenediamine (EDA) was added as a curing agent for dry spinning to produce the as-spun fibers. Heat curing and microwave curing treatments were performed to obtain phenolic epoxy fibers. Using Fourier transform infrared spectroscopy to study the structural changes during the fiber curing process revealed that the amino groups in EDA opened the epoxy groups to generate the hydroxyl groups. The hydroxyl groups can further react with the epoxy groups, which accelerate the curing reaction. Thermogravimetric analysis (TGA) results showed a higher residual carbon degree in the fibers after curing. Mechanical property testing demonstrated a significant improvement in the mechanical properties of the fibers. By modifying the blending and optimizing the curing process, the heat resistance of the fibers was successfully improved, resolving the issue of poor mechanical properties in the high-ortho phenolic epoxy fibers (HPEFs).

Flame retardant composite phase change materials with MXene for lithium-ion battery thermal management systems

A high-quality thermal management system is crucial for addressing the thermal safety concerns of lithium ion batteries. Despite the utilization of phase change materials (PCMs) in battery thermal management, there is still a need to raise thermal conductivity, shape stability, and flame retardancy in order to effectively mitigate battery safety risks. This study investigates a flame-retardant PCM composed of polyethylene glycol, expanded graphite, MXene, APP (ammonium polyphosphate), and ZHS (Zinc hydroxy stannate). The properties of the PCM and its thermal management performance during the operation of batteries are explored and evaluated. The results demonstrate that the incorporation of MXene enhances both the enthalpy of phase transition and thermal conductivity of PCM. Furthermore, the synergistic flame retardancy of APP and ZHS increases the carbon residue content, enabling PCM to achieve a V0 flame retardant rating. PCM exhibits a noticeable cooling effect on the battery temperature, reducing the highest temperature of the battery module to 57.03 °C during 3C discharge while maintaining a temperature difference of within 5 °C. This research contributes valuable insights into the potential use of PCMs with MXene in thermal management systems for batteries, with the aim of improving lithium batteries safety during operation.

Liquid lithium corrosion of SiC/SiC composites

Silicon carbide fibre reinforced silicon carbide matrix composite (SiC/SiC) is a key structural material for fusion reactors to allow high temperature operation of liquid lithium breeder blankets. This research investigated the corrosion behaviour of two SiC/SiC composites (using Tyranno SA3 and SA4 fibres) immersed in static liquid lithium at 600 °C for 100 h. Utilizing immersion tests and advanced microstructural analysis, the study reveals considerable corrosion in SiC/SiC composites, particularly in local areas enriched with residual carbon or oxygen. The interface carbon layer, while enhancing mechanical properties, induces preferential sites for corrosion cracking, diminishing the material's corrosion resistance. This study offers critical insights into the corrosive interaction between SiC/SiC composites and liquid lithium, highlighting the need for manufacturing process optimization and exploration of alternative interface layers, protective coatings, or avoiding contact between SiC/SiC and molten lithium in breeder blanket system.

Microwave-induced combustion for further determination of potentially toxic elements in honey by ICP-MS.

Microwave-induced combustion (MIC) was proposed in this study for honey decomposition aiming for As, Cd, Hg, and Pb determination by inductively coupled plasma mass spectrometry (ICP-MS). Sample mass (up to 1.0g), absorbing solution (0.5 to 14.4mol L-1 HNO3, and H2O), heating program, and combustion aids were evaluated. The Eurachem guidelines were used for method validation. The proposed method enabled combustion of a high sample mass (0.8g of honey, with 0.4g of microcrystalline cellulose and 100 µL of 6mol L-1 NH4NO3) using 6mL of an absorbing solution consisting of 1mol L-1 HNO3, which resulted in low residual carbon in solution (< 25mg L-1). Honey samples from different geographical origins were analyzed. Results showed no significant difference in comparison to other two microwave decomposition methods, based on microwave-assisted wet digestion with single reaction chamber (MAWD-SRC) and microwave-assisted wet digestion (MAWD). Standard addition experiments resulted in recoveries higher than 98%. The limits of detection ranged from 1.10 (As) to 4.60ngg-1 (Pb). In addition to using only diluted reagents and resulting in digests virtually free of interferences, the proposed method was faster (< 30min) than most of those presented in the literature.

Synthesis of Fe–N doped porous carbon/silicate composites regulated by minerals in coal gasification fine slag for synergistic electrocatalytic treatment of phenolic wastewater

Coal gasification fine slag (CGFS), as a difficult-to-dispose solid waste in the coal chemical industry, consists of minerals and residual carbon. Due to the aggregate structure of minerals blocking pores and encapsulating active substances, the high-value utilization of CGFS still remains a challenge. Based on the intrinsic characteristics of CGFS, this study synthesized Fe–N doped porous carbon/silicate composites (Fe-NC) by alkali activation and pyrolysis for electrocatalytic degradation of phenolic wastewater. Meanwhile, minerals were utilized to regulate the surface chemical and pore structure, turning their disadvantages into advantages, which caused a sharp increase in m-cresol mineralization. The positive effect of minerals on composite properties was investigated by characterization techniques, electrochemical analyses and density functional theory (DFT) calculations. It was found that the mesoporous structure of the mineral-regulated composites was further developed, with more carbon defects and reactive substances on its surface. Most importantly, silicate mediated iron conversion through strong interaction with H2O2, high work function gradient with electroactive iron, and excellent superoxide radical (•O2−) production capacity. It effectively improved the reversibility and kinetics of the entire electrocatalytic reaction. Within the Fe-NC311 electrocatalytic system, the m-cresol removal rate reached 99.55 ± 1.24%, surpassing most reported Fe–N-doped electrocatalysts. In addition, the adsorption and electrooxidation experiment confirmed that the synergistic effect of Fe–N doped porous carbon and silicate simultaneously promoted the capture of pollutants and the transformation of electroactive molecules, and hence effectively shortened the diffusion path of short-lived radicals, which was further supported by molecular dynamics simulation. Therefore, this research provides new insights into the problem of mineral limitations and opens an innovative approach for CGFS recycling and environmental remediation.

Label-Free Quantitative Analysis of Pig Liver Proteome after Hepatitis E Virus Infection.

Hepatitis E represents an emerging zoonotic disease caused by the Hepatitis E virus (HEV), for which the main route of transmission is foodborne. In particular, infection in humans has been associated with the consumption of contaminated undercooked meat of pig origin. The aim of this study was to apply comparative proteomics to determine if porcine liver protein profiles could be used to distinguish between pigs seropositive and seronegative for HEV. Preliminarily, an ELISA was used to evaluate the presence of anti-HEV antibodies in the blood serum of 136 animals sent to slaughter. Among the analyzed samples, a seroprevalence of 72.8% was estimated, and it was also possible to identify 10 animals, 5 positive and 5 negative, coming from the same farm. This condition created the basis for the quantitative proteomics comparison between homogeneous animals, in which only the contact with HEV should represent the discriminating factor. The analysis of the proteome in all samples of liver exudate led to the identification of 554 proteins differentially expressed between the two experimental groups, with 293 proteins having greater abundance in positive samples and 261 more represented in negative exudates. The pathway enrichment analysis allowed us to highlight the effect of the interaction between HEV and the host biological system in inducing the potential enrichment of 69 pathways. Among these, carbon metabolism stands out with the involvement of 41 proteins, which were subjected to interactomic analysis. This approach allowed us to focus our attention on three enzymes involved in glycolysis: glucose-6-phosphate isomerase (GPI), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and fructose-bisphosphate aldolase A (ALDOA). It therefore appears that infection with HEV induced a strengthening of the process, which involves the breakdown of glucose to obtain energy and carbon residues useful for the virus's survival. In conclusion, the label-free LC-MS/MS approach showed effectiveness in highlighting the main differences induced on the porcine liver proteome by the interaction with HEV, providing crucial information in identifying a viral signature on the host metabolism.