Residual Carbon Research Articles

Enhanced intrinsic thermal conductivity of liquid crystalline polyester dispersed films through hydrogen bond interaction

Polymer-dispersed liquid crystal (MHxFy) films comprising liquid crystal polymer (LCPH and LCPF) were successfully obtained by the method of solution casting & thermal compressing. At a LCPH mass fraction of 67 %, thermal conductivity (λ) value in through-plane (λ⊥) and in-plane (λ∥) direction of MH2F1 films reach up to 0.305 W/(m·K) and 2.879 W/(m·K), respectively. In comparison to pure LCPF, the thermal conductivity of MH2F1 exhibited an increase of 4.42 times, which is 14.4 times than that of conventional thermoplastics. Meanwhile, the crystallinity of MHxFy films around 50 % which is indicate the crystal phase become more integrated and regular. The FTIR spectra reveals a significant blue shift (3432 cm−1 to 3421 cm−1) in the absorption peak of the –OH group in MH2F1, suggesting a robust interaction between LCPF and LCPH. The primary cause of elevated thermal conduction in these films was determined to be the consistent presence of “thermal bridges” and a high degree of crystallinity. Furthermore, the T5%, Tmax and residual carbon at 800 °C of MH2F1 were 347.8 °C, 409.4 °C and 8 %, respectively. This is attributed to the ordered distribution of LCPH in LCPF matrix through hydrogen bonding interaction, forming an interpenetrating network of LCPF-LCPH. The result show that MHxFy films demonstrating superior intrinsic thermal conductivities, thermal stabilities, and mechanical properties.

Application of aminotrimethylphosphonic acid modified starch‐based flame retardant in cellulosic paper

AbstractThe development of green and efficient bio‐based flame retardants is very important for the development of flame‐retardant cellulosic paper. In this study, a novel type of starch‐based synergistic flame retardant (SAPU) was prepared using corn starch as carbon sources, amino trimethylphosphonic acid, and urea as phosphorus and nitrogen sources through the one‐pot method. Subsequently, the flame‐retardant cellulosic paper was prepared by impregnation, and the flame retardancy of the cellulosic paper was evaluated by vertical combustion, limiting oxygen index (LOI), and thermogravimetric analysis. The results demonstrated that the SAPU exhibited a favorable flame‐retardant effect on cellulosic paper. At a concentration of 25.0%, the vertical burning residue of flame‐retardant paper accounted for 49.16% of the total length of the paper sample, while the LOI was 39.4%. The tensile strength and burst index of cellulosic paper were found to be decreased by 6.36% and 19.1%, respectively, in comparison to the base paper. Conversely, the ring crush strength was observed to be increased by 156.2%. The carbon residue rate at 700°C under a nitrogen atmosphere rose from 11.56% of the base paper to 28.77% of the flame‐retardant paper. The flame‐retardant SAPU effectively improved the thermal stability of cellulosic paper.

Fabrication of nickel phytate modified bio-based polyol rigid polyurethane foam with enhanced compression-resistant and improved flame-retardant

A bio-based flame retardant nickel phytate (PA-Ni) was synthesized and combined with soybean oil-based polyol (SO) to create a green rigid polyurethane foam (RPUF) with enhanced compressive strength, good thermal stability and flame retardant. The results showed that the RPUF-SO2/Ni3 with 3 wt% PA-Ni had the highest initial and termination temperature, maximum thermal decomposition rate temperature and carbon residue, and better thermal stability. Its limiting oxygen index was increased by 2.6% compared with RPUF-SO2 without PA-Ni added, and the peak heat release rate (PHRR) and total heat release rate (THR) were reduced by 14.92% and 19.92%, respectively. In addition, RPUF-SO2/Ni3 had the lowest Ds under the conditions of flame (18.90) and flameless (22.41), and had the best smoke suppression effect. And the compressive strength of RPUF-SO/Ni3 was significantly enhanced by the addition of PA-Ni. The results show that the improvement of flame retardancy of RPUF is mainly the result of the combined effect of gas-phase and condensed-phase flame retardancy, among which the flame retardancy of RPUF-SO/Ni3 was the best. The current findings offer a practical way to produce green and low-carbon RPUF as well as promising prospects for the material's safe application.

Effect of dissolution for black carbon on the adsorption capacity for methylene blue: Equilibrium, kinetics and thermodynamics

Black carbon was widely researched due to its significant role on the global carbon cycle and contaminant transport, and most people were concerned about the property of the dissolved black carbon from black carbon. In this work, we focused on the research of the residual those of black carbon. Two kinds of black carbon originated from peanut shell and bamboo were prepared and the corresponding residual black carbons were also obtained by the ultrasonic dissolution process. It was found the chemical and structure properties of residual black carbon changed a lot compared to black carbon. Using methylene blue as a target contaminant, the adsorption capacity of methylene blue by the residual black carbon was greater than that of black carbon. The adsorption capacity of black carbon-bamboo for methylene blue increased from 11.1 mg/g to 16 mg/g after the dissolution process, and the adsorption capacity of black carbon-peanut shell for methylene blue increased from 14 mg/g to 23 mg/g. The various influencing factors, such as the pH, initial concentration, temperature and adsorbent dosage, were systematically studied. The black carbons derived from peanut shell before and after the ultrasonic dissolution process both showed greater adsorption capacities for methylene blue. To further elucidate the methylene blue adsorption process, different kinds of isotherm and kinetics models were applied to simulate the experimental data. The results indicated that the Langmuir isotherm model was suitable to all the carbons before and after the ultrasonic dissolution process, and the pseudo-second-order model showed great simulation for the adsorption of methylene blue. In addition, the analysis of the thermodynamic study revealed that the adsorption processes of methylene blue were endothermic and spontaneous. Overall, results obtained from this work revealed the black carbon after been dissolved showed better adsorption capacity for contaminant.

Improving thermal conductivity of Al/SiC composites by post-oxidization of reaction-bonded silicon carbide preforms

High thermal conductivity aluminium-based silicon carbide (Al/SiC) composites were successfully fabricated through post-oxidization of reaction-bonded silicon carbide preforms (RS preforms), utilizing vacuum pressure infiltration technology. The study investigated the regulation of interfacial reactions in conventional sintering and reaction sintering. Conventional sintering introduced a large amount of SiO2, which negatively impacted the thermal conductivity of the Al/SiC composite, but the reaction sintering not. The proposed post-oxidization treatment of RS preforms effectively removed residual carbon from the SiC particle surfaces, thereby forestalling the formation of Al4C3. Furthermore, the post-oxidization treatment effectively formed lightweight SiO2 deposits onto the surface of SiC particles, improving Al-SiC interfacial wettability and reducing thermal resistance, thereby enhancing composite thermal conductivity. Notably, the thermal conductivity of the post-oxidized sample exhibited an increase of 6.5% compared to the untreated sample. The study also evaluated the impact of particle size distribution on volume fraction and thermal properties. The optimized Al/SiC composites yielded thermal conductivity, coefficient of thermal expansion, bending strength, and Young’s modulus values of 237.3 W/m K, 8.5 × 10−6/°C, 325 MPa, and 75.9 GPa, respectively.

The accumulation of fungal not bacterial residue carbon is management-dependent under conventional and organic practices in apple-orchard soil

Organic orchard management has been widely adopted to enhance soil fertility by improving the sequestration of soil organic carbon (SOC). Microbial residue carbon plays an essential role in SOC accumulation; nevertheless, how fungal and bacterial residue carbon (FRC and BRC) changes with different orchard management practices (organic vs. conventional) and the factors influencing their accumulation remain poorly understood. In this study, we quantified the FRC and BRC in the two management practices, compiled this data with the comparisons of plant, soil and microbial properties, and the dominant factor affecting their sequestration was ascertained with a 4-year orchard experiment on the Jiaodong Peninsula. Compared with conventional management, organic management significantly enhanced SOC and the accumulation of FRC and BRC, while it did not alter the contribution of FRC or BRC to SOC. Furthermore, we identified that the primary determinant affecting FRC varied with management type: Plant (AGR, BGG)-soil (SOC, density)-microbe (Nitrospirae) collectively governed FRC in organic soil, whereas soil (pH, density) and microbial (Ascomycota) properties regulated FRC in conventional soil. Nitrospirae abundance and soil pH played pivotal roles in FRC accumulation under organic and conventional management, respectively. Meanwhile, the primary factor influencing BRC was independent of management type: Soil and microbial properties consistently served as the principal determinants of BRC in both management systems, with soil pH and clay being the pivotal factors in organic and conventional managements, respectively. These findings illustrate the divergent regulatory mechanisms of FRC and BRC in organic and conventional management, thereby enhancing our comprehension of microbial-mediated SOC sequestration in organic orchard management.

Assessment of surface Water Quality for Drinking and Irrigation Purposes for Two Dams in the Semi-Arid Region of Northeast Algeria

<p>The surface water quality of Timgad and Yabous dams in the semi-arid region of northeast Algeria was evaluated using physicochemical data collected monthly from May 2023 to April 2024. Parameters including temperature (T), pH, electrical conductivity (EC), total dissolved solids (TDS), chloride (Cl⁻), sulfate (SO₄²⁻), bicarbonate (HCO₃⁻), nitrate (NO₃⁻), sodium (Na⁺), potassium (K⁺), calcium (Ca²⁺), and magnesium (Mg²⁺) were analyzed to assess suitability for drinking and irrigation purposes. For drinking purposes, the Water Quality Index (WQI) and CCME-WQI were employed. Results showed permissible WQI values for Timgad Dam throughout the year, with Yabous Dam exhibiting good quality consistently. However, CCME-WQI classified Timgad Dam as marginal and Yabous Dam as fair annually, indicating a need for caution, particularly for Timgad Dam. For irrigation purposes, various indices including Sodium Adsorption Ratio (SAR), Sodium Percentage (NA%), Residual Sodium Carbonate (RSC), Permeability Index (PI), Potential Salinity (PS), Kelly’s Ratio (KR), Residual Sodium Bicarbonate (RSBC), and Magnesium Hazard (MH) were utilized. While both dams generally demonstrated suitable classes for irrigation, Timgad Dam exhibited unsuitability due to elevated Potential Salinity values, attributed to high chloride and sulfate concentrations that probably come from anthropogenic activities and natural processes, and MH values were unsuitable for both dams throughout the year.</p>

Predicting irrigation water quality indices in a typical mining dominated area in the Upper West region of Ghana using multiple machine learning techniques

The quality of groundwater resources in artisanal mining districts in Ghana is under threat due to pollution; rendering the resource unsafe for drinking and irrigation purposes. This makes the assessment of the quality of groundwater resources a relevant aspect of groundwater studies as it informs decision making and monitoring. This study adopts 3 Machine Learning (ML) models, Support Vector Regression (SVR), Gradient Boost Regression (GBR), and Artificial Neural Network (ANN), to evaluate a variety of irrigation water quality metrics such as Sodium Percentage (Na%), Soluble Sodium Percentage (SSP), Sodium Adsorption Ratio (SAR), Residual Sodium Carbonate (RSC), Permeability Index (PI), Pollution Index of Groundwater (PIG), Kelly’s Ratio (KR), and Magnesium Hazard (MH). 105 samples were collected from a mining area in Northern Ghana and analysed through traditional methods. The Irrigation Water Quality Indices (IWQIs) demonstrate that all water samples are suitable for use as irrigable water with the exception of MH, Na%, PI, and PIG which revealed that 69.52%, 8.57%, 29.52%, and 3.81% are inappropriate for irrigation. SVR, GBR and ANN were used to establish important factors that may influence IWQIs in the area. The measured data was used as independent variables, and the derived IWQIs, the dependent variables. The results revealed that ANN, GBR, and SVR are all viable options for the prediction of IWQIs, but GBR exhibited variable performance in some indices making it lack consistency and thus falls a bit short compared to ANN and SVR. SVR models overall performed best with SVR-RSC having the highest accuracy.

Syringaldehyde‐DOPO derivative for enhancing flame retardancy and mechanical properties of epoxy resin

AbstractWith the wide application of epoxy resins in adhesives, electronic packaging materials, and aerospace fields, it is necessary to prepare high‐performance flame‐retardant epoxy resins to reduce the fire risk caused by their flammability. In this study, the rigid structure intermediate Schiff base (DMDA‐SH) was synthesized by condensation reaction of syringaldehyde (SH) with O‐Tolidine (DMDA). Then, DMDA‐SH‐DOPO, a novel P/N‐structured biobased flame‐retardant curing agent, was synthesized by addition reaction with 9,10‐dihydro‐9‐oxaza‐10‐phosphame‐10‐oxide (DOPO) and was applied to the preparation of intrinsic flame‐retardant epoxy resin. As expected, DMDA‐SH‐DOPO has good flame‐retardant properties due to the synergistic action of N/P elements. Epoxy resin with only 2.5% DMDA‐SH‐DOPO (P = 0.16%) can pass the UL‐94 V‐0 test. Compared with DGEBA/DDM, DMDA‐SH‐DOPO‐7.5's (P = 0.49%) peak heat release rate was reduced by 48.4% and the limiting oxygen index (LOI) reached 27%, making it a flame‐retardant material. From the point of view of carbonaceous residue performance, the expansion height of carbon residue after DMDA‐SH‐DOPO‐7.5 combustion is significantly increased, and the amount of carbon residue at 800°C is increased by 36.4%. In addition, appropriate DMDA‐SH‐DOPO can effectively improve the bending property of epoxy resin. This study provides a new idea for preparing renewable high‐performance intrinsic flame‐retardant epoxy resin.

Demethylation C–C coupling reaction facilitated by the repulsive Coulomb force between two cations

Carbon chain elongation (CCE) is normally carried out using either chemical catalysts or bioenzymes. Herein we demonstrate a catalyst-free approach to promote demethylation C–C coupling reactions for advanced CCE constructed with functional groups under ambient conditions. Accelerated by the electric field, two organic cations containing a methyl group (e.g., ketones, acids, and aldehydes) approach each other with such proximity that the energy of the repulsive Coulomb interaction between these two cations exceeds the bond energy of the methyl group. This results in the elimination of a methyl cation and the coupling of the residual carbonyl carbon groups. As confirmed by high-resolution mass spectrometry and isotope-labeling experiments, the C–C coupling reactions (yields up to 76.5%) were commonly observed in the gas phase or liquid phase, for which the mechanism was further studied using molecular dynamics simulations and stationary-point calculations, revealing deep insights and perspectives of chemistry.

Enhancing mechanical properties and density of WC-Co with pressureless sintering via shell structure binder jetting additive manufacturing

The binder jetting (BJT) additive manufacturing (AM) process is suitable for producing complex WC-Co cemented carbide parts. To achieve near-full-density in the final parts, the hot isostatic pressing (HIP) sintering process is typically employed to enhance densification. However, HIP sintering requires high equipment specifications and is relatively more costly compared to conventional pressureless sintering. To improve the density of WC-Co parts printed by BJT AM under the pressureless sintering environment, the shell structure printing method was used in this study. The shell structure printing only jets binder to the model's outer profile, creating a shell that encapsulates the central powder, mitigates binder pyrolysis and residual effects on particle densification, and enhances post-sintering density. In this work, the effect of shell thickness, binder type, and printing layer thickness on the density and mechanical properties of the WC-12Co parts under pressureless sintering conditions were investigated. The results show that the density and mechanical properties of the WC-12Co parts significantly improved with the decreasing shell thickness. Specifically, the WC-12Co printed using shell structure achieves a relative density of over 98% and a transverse rupture strength (TRS) of 1954 MPa after pressureless sintering, a result comparable to BJT printed samples treated with HIP sintering. Moreover, the results indicate using a binder with lower residual carbon content and smaller printing layer thickness has a more positive effect on improving density and mechanical strength when employing the shell structure printing method. Microstructure morphology and phase analysis results indicate that the shell structure printing method does not affect the growth of WC grains in the shell and center regions, nor does it influence its phase composition. The shell structure printing method offers a new approach to the manufacturing of near-full-dense WC-Co materials using the BJT process.

Smoke Suppression Properties of Fe2O3 on Intumescent Fire-Retardant Coatings of Styrene–Acrylic Emulsion

The intumescent flame-retardant coatings were prepared using ammonium polyphosphate (APP), pentaerythritol (PER), melamine (MEL), styrene–acrylic emulsion, and iron oxide yellow (FeOOH) as the base material. A cone calorimeter (CCT), smoke density meter (SDA), and scanning electron microscope (SEM) were employed to investigate the smoke suppression and flame retardancy of FeOOH in intumescent fire-retardant coatings. The thermal degradation performance of intumescent fireproofing coatings with varying FeOOH content was investigated through thermogravimetric analysis (TGA). The structure of the carbon slag in the CCT test was analyzed using a scanning electron microscope (SEM). The results of the cone calorimeter (CCT) experiments demonstrated that FeOOH significantly reduced the heat release rate (HRR), total heat release rate (THR), smoke production rate (SPR), and total smoke release rate (TSR) of the coating, while simultaneously increasing the carbon residue rate of the coating. The smoke density analysis (SDA) results demonstrate that adding FeOOH can effectively reduce smoke generation, regardless of whether a pilot flame is used. TGA results demonstrate that FeOOH can enhance the weight of coke residue at elevated temperatures. SEM results indicate that incorporating FeOOH resulted in a more compact coke residue. According to these findings, among all the samples, those containing 2 wt% FeOOH showed low levels of HRR, THR, SPR, and TSR and high levels of SOD, which proves that FeOOH can be used as a smoke inhibitor in flame-retardant coatings.

Spatial variation of methane oxidation and carbon dioxide sequestration in landfill biogeochemical cover

ABSTRACT The study investigated the spatial variation of potential methane (CH4) oxidation and residual carbon dioxide (CO2) sequestration in biogeochemical cover (BGCC) system designed to remove CH4, CO2, and hydrogen sulfide (H2S) from landfill gas (LFG) emissions. A 50 cm x 50 cm x 100 cm tank simulated BGCC system, comprising a biochar-amended soil (BAS) layer for CH4 oxidation, a basic oxygen furnace (BOF) slag layer for CO2 and H2S sequestration, and an upper topsoil layer. Synthetic LFG was flushed through the system in five phases, with each corresponding to different compositions and flow rates. Following monitoring, the system was dismantled, and samples were extracted from different depths and locations to analyze spatial variations, focusing on moisture content (MC), organic content (OC), pH, and electrical conductivity (EC). Additionally, batch tests on selected samples from BAS and BOF slag layers were performed to assess potential CH4 oxidation and residual carbonation capacity. The aim of study was to evaluate the BGCC's effectiveness in LFG mitigation, however this study focused on assessing spatial variations in physico-chemical properties, CH4 oxidation in the BAS layer, and residual carbonation in the BOF slag layer. Findings revealed CH4 oxidation in the BAS layer varied between 22.4 and 277.9 µg CH4/g-day, with higher rates in the upper part, and significant spatial variations at 50 cm below ground surface (bgs) compared to 85 cm bgs. The BOF slag layer showed a residual carbonation capacity of 40-49.3 g CO2/kg slag, indicating non-uniform carbonation. Overall, CH4 oxidation and CO2 sequestration capacities varied spatially and with depth in the BGCC system.

Enhancing refinery heavy oil fractions analytical performance through real-time predicative modeling.

This study introduces a suite of robust models aimed to advance the determination of physiochemical properties in heavy oil refinery fractions. By integrating real-time analytical technique inside the refinery analysis, we have developed a single analyzer capable of employing six partial least square regression equations. These designed models enable to provide real-time prediction of critical petroleum properties, such as sulfur content, micro carbon residues (MCR), asphaltene content, heating value, and the concentrations of nickel and vanadium metals. Specifically tailored for heavy oil in refinery feeds with an American petroleum institute (API) gravity range of 3° to 32° and sulfur content of 2.8 to 5.5 wt%, the models streamline the analysis process within refinery operations, bridging the gap between catalytic and non-catalytic processes across refinery units. The accuracy of our physiochemical prediction models has been validated against American Society for Testing and Materials (ASTM) standards, demonstrating their capability to deliver precise real-time property values. This approach not only enhances the efficiency of refinery analysis but also sets a new standard for the monitoring and optimization of heavy oil processing in real-time approach.

DETERMINATION OF THE FEATURES OF THERMAL DECOMPOSITION OF SUNFLOWER HUSK IN A FLUIDIZED BED

Sunflower husk (SH) is a plant waste fuel. The carbon content in different samples of SH ranges from 40.5% to 54.5% in an operating state, with ash content ranging from 1.5% to 8.5%, moisture content ranging from 6.9% to 9.5%, chlorine content ranging from 0.05% to 0.3%, and lower heating value ranging from 14.5 MJ/kg to 20.5 MJ/kg. These characteristics make it a suitable substitute for fossil fuels in power boilers. Waste-to-energy (WTE) technologies are rapidly developing worldwide, offering the potential for generating renewable energy from waste, including agricultural and food industry waste such as SH. According to our estimates, Ukraine has an annual energy potential of approximately 3.4 million tons of SH or about two million tons of fuel equivalent. Approximately half of this volume is currently being burned in oil extraction plants' boilers; however, up to one million tons of SH end up in landfills annually, resulting in significant energy losses. To develop new and improve existing WTE technologies that utilize SH as a fuel source, it's essential to understand the thermal processing characteristics of SH under conditions similar to those found in different zones within real power boilers - specifically the heating of fuel particles at rates up to 500 °C/s over a temperature range of 500–1000 °C. In this study, we aimed to investigate the thermal processing characteristics by subjecting SH particles within a laboratory fluidized bed reactor to high-speed heating within the aforementioned temperature range. During rapid heating between 500–1000 °C temperatures range, SH particles undergo conversion into volatile compounds and solid carbon residue. Two distinct stages can be observed on the dynamic yield curves for volatiles. The release and burnout of volatiles occurs during the first stage while the second stage involves coke ash residue burnout. We obtained empirical temperature-dependents for total heat treatment time and carbon residue burnout time under fast heating conditions in the investigated temperature range. The stage of carbon residue combustion is the most enduring and determines the overall duration of thermal treatment. This stage determines the degree of fuel transformation, especially in cases where low-reactivity carbon residue enters the low-temperature combustion chamber area of the boiler. The obtained regularities have practical significance in designing combustion chambers for thermal processing of sunflower husk.

Characterization of oxygen initiation process in the autothermic pyrolysis in-situ conversion of Huadian oil shale

The oxygen initiation process, one of the key processes in the early stage of the autothermic pyrolysis in-situ conversion technology, has not been deeply investigated, which seriously limits its development. In this study, the reaction behaviors, kinetic parameters, heat and product release characteristics during the isothermal oxygen initiation process of Huadian oil shale in O2/N2 mixtures with different oxygen concentrations and initiation temperatures were investigated via TG/DSC-FTIR. The results show that the samples exhibit three different reaction behaviors during the initiation stage, consisting of two main parts, i.e., the oxidative weight-gain and the oxidative reaction phases. The former phase is mainly characterized by the oxygen addition reaction that produces oxidizing groups which increase the sample mass. And the latter stage consists of two main subreactions. The first subreaction involves the oxidative cracking and pyrolysis of oxidizing groups and kerogen to produce fuel deposits such as residual carbon, while the second subreaction focuses on the oxidation of the resulting fuels. Furthermore, increasing the oxygen concentration significantly promotes the above reactions, leading to an increase in the reaction intensity and reaction rate. Owing to the combined effect of oxygen concentration and residual organic matter content, the total heat release increases with the increasing initiation temperature and reaches its maximum at 330–370 °C. In addition, the preheating stage primarily produces hydrocarbon gases, while the initiation stage predominantly generates CO2. As the preheating temperature increases, the CO2 output intensifies, the required reaction time shortens, and the release becomes more concentrated. Based on these findings, a reaction mechanism for the oxygen initiation process of Huadian oil shale was proposed, and recommendations were provided for optimizing the construction process.

Improving tension fatigue performance of gray cast iron by LSPwC-induced gradient structure and carbon diffusion

HT250 Gray cast iron (GCI) commonly utilized in diesel engine cylinders, is susceptible to fatigue failure under alternating stress conditions. To address this issue, the investigation involved the application of laser shock peening without coating (LSPwC) on HT250 GCI to assess its impact on the high cycle tension fatigue properties of the material. Both experimental and simulation methodologies were employed to analyze the effects of LSPwC on residual stress, microhardness, and microstructure in HT250 GCI. The LSPwC resulted in a substantial 29% enhancement in the high cycle tension fatigue limit of the HT250 GCI, which is attributed to a synergistic combination of factors induced by LSPwC, including high-amplitude compressive residual stresses, elevated microhardness, grain refinement, and carbon diffusion. This study contributes valuable insights into the reinforcement of complex cast components.

Canopy and understory nitrogen additions differently affect soil microbial residual carbon in a temperate forest.

Atmospheric nitrogen (N) deposition in forests can affect soil microbial growth and turnover directly through increasing N availability and indirectly through altering plant-derived carbon (C) availability for microbes. This impacts microbial residues (i.e., amino sugars), a major component of soil organic carbon (SOC). Previous studies in forests have so far focused on the impact of understory N addition on microbes and microbial residues, but the effect of N deposition through plant canopy, the major pathway of N deposition in nature, has not been explicitly explored. In this study, we investigated whether and how the quantities (25 and 50 kg N ha-1 year-1) and modes (canopy and understory) of N addition affect soil microbial residues in a temperate broadleaf forest under 10-year N additions. Our results showed that N addition enhanced the concentrations of soil amino sugars and microbial residual C (MRC) but not their relative contributions to SOC, and this effect on amino sugars and MRC was closely related to the quantities and modes of N addition. In the topsoil, high-N addition significantly increased the concentrations of amino sugars and MRC, regardless of the N addition mode. In the subsoil, only canopy N addition positively affected amino sugars and MRC, implying that the indirect pathway via plants plays a more important role. Neither canopy nor understory N addition significantly affected soil microbial biomass (as represented by phospholipid fatty acids), community composition and activity, suggesting that enhanced microbial residues under N deposition likely stem from increased microbial turnover. These findings indicate that understory N addition may underestimate the impact of N deposition on microbial residues and SOC, highlighting that the processes of canopy N uptake and plant-derived C availability to microbes should be taken into consideration when predicting the impact of N deposition on the C sequestration in temperate forests.

Eco-friendly lactose/tannin-based binder in MgO–C refractories produced from MgO–C recyclate

This study deals with the design and development of a new generation of MgO–C refractory material implementing spent MgO–C recyclate as a partial replacement of fresh raw materials, and a non-hazardous environment-friendly lactose- and tannin-based binder system. Throughout the experimental campaign the used MgO–C recyclate, which was received in three size fractions, was analysed, and building on the obtained results, multiple batches of various compositions of next-generation MgO–C bulks were prepared. These bulks varied in the ratio between the individual size fractions of the MgO–C recyclate, the ratio between the individual binder components and the amount of water used during the preparation of the raw material batches. The bulk samples were prepared in the form of cylinders through uniaxial pressing, cured and coked, and studied in terms of their cold crushing strength, microstructural parameters, thermal behaviour, residual carbon content, and microstructure. The proposed next generation of MgO–C composites represents a potential eco-friendly alternative to MgO–C refractories prepared from traditional raw materials while utilizing waste material which would otherwise end up landfilled.

GROUNDWATER QUALITY ASSESSMENT FOR RESIDENTIAL AND IRRIGATION PURPOSES: A CASE STUDY OF FUTUK AND ITS ENVIRONS, NORTHERN BENUE TROUGH, NORTHEAST NIGERIA

This research assesses the suitability of groundwater quality in the region for residential and agricultural use. To evaluate the water quality for domestic purposes, 15 samples of groundwater were taken and tested for various physicochemical parameters including pH, electrical conductivity (EC), total dissolved solids (TDS), calcium (Ca), magnesium (Mg), sodium (Na), potassium (K), sulfate (SO4), chloride (Cl), bicarbonate (HCO3), carbonate (CO3), and nitrate (NO3). The quality of irrigation water was evaluated using several parameters: permeability index (PI), sodium absorption ratio (SAR), total hardness (TH), residual sodium carbonate (RSC), and water quality index (WQI). Piper diagrams, Gibbs diagrams, and the chloro-alkaline index were used to determine groundwater facie classification and ion exchange mechanisms. When compared to the WHO 2011 standard, the physiochemical parameters are within the appropriate limits, with the exception of EC and NO3, which revealed excessive values in some samples. All of the measured parameters are suitable for irrigation activities. According to the Kelly index, there is just one sample that is inappropriate for irrigation. The predominant groundwater type in the area is calcium chloride, with sodium chloride constituting the second most common groundwater facies. The hydrochemical mechanism that regulates the local groundwater chemistry is reverse ion exchange. This indicates a positive index, resulting from the exchange of sodium (Na) and potassium (K) in the groundwater with calcium (Ca) and magnesium (Mg) in the aquifer components.