Greenhouse gas mitigation and soil carbon stabilization potential of forest biochar varied with biochar type and characteristics.

Biochar is increasingly used in climate-smart agriculture, yet its impact on greenhouse gas (GHG) emissions and soil carbon (C) sequestration remains poorly understood. This study examined biochar-mediated changes in soil properties and their contribution to C stabilization and GHG mitigation by evaluating four types of biochar. Soil carbon dioxide (CO2) and nitrous oxide (N2O) emissions, soil chemical and biological properties, and soil organic carbon (SOC) mineralization kinetics were monitored using greenhouse, laboratory, and modeling experiments. Three pine wood biochars pyrolyzed at 460 °C (PB-460), 500 °C (PB-500), 700 °C (PB-700), and one pine bark biochar from gasification at 760 °C (GB-760) were added into soil at 1 % w/w basis. Soils amended with biochar were used to cultivate sorghum for three months in a greenhouse, followed by three months of laboratory incubation. Data obtained from laboratory incubation was modeled using various statistical approaches. The PB-500 and PB-700 reduced cumulative N2O-N emissions by 68.5 % and 73.9 % and CO2 equivalent C emissions by 66.9 % and 72.4 %, respectively, compared to unamended control. The N2O emissions were positively associated with soil nitrate N, available P, and biochar ash content while negatively associated with SOC. The CO2 emission was negatively related to biochar C:N ratio and volatile matter content. Biochar amended soils had 49.2 % (PB-500) to 87.7 % (PB-700) greater SOC and 22.9 % (PB-700) to 48.1 % (GB-760) greater sorghum yield than the control. While PB-700 had more saprophytes than the control, the GB-760 yielded a greater yield than biochars prepared by pyrolysis. Microbial biomass C was 7.23 to 23.3 % greater in biochar amended soils than in control. The double exponential decay model best explained the dynamics of C mineralization, which was associated with initial soil nitrate N and available P positively and total fungi and protozoa biomass negatively. Biochar amendment could be a climate smart agricultural strategy. Pyrolysis pine wood biochar showed the greatest potential to reduce GHG emissions and enhance SOC storage and stability, and gasification biochar contributed more to SOC storage and increased crop yield.

Magnesium doped biochar for simultaneous adsorption of phosphate and nitrogen ions from aqueous solution.

Phosphorus (P) and Ammonium Nitrogen (N) are essential nutrients for plants and environmental stability. However, their excess in water causes eutrophication, damaging aquatic ecosystems. While adsorption is a promising solution, finding affordable and efficient adsorbents remains a challenge. In this study, magnesium (Mg), iron (Fe), and Mg/Fe doped biochars (BC) adsorbents were synthesized, and evaluated for adsorption of individual P and N and a P + N mixture from a solution and wastewater from a wastewater treatment plant. Compared to other adsorbents, Mg/BC showed excellent performance in adsorbing phosphorus (P) and ammonium nitrogen (N) from aqueous solutions. It demonstrated a large adsorption capacity of 64.65 mg/g and 62.50 mg/g from individual P and N solutions, and 30.3 mg/g and 27.67 mg/g from the P and N mixture solution, respectively. In addition, Mg/BC efficiently removed P and N from real-life wastewater. In the real wastewater, P and N removal efficiencies reached 88.30% and 59.36%, respectively. Kinetics analysis revealed that the pseudo-second-order model accurately described the adsorption of phosphorus (P) and ammonium nitrogen (N) in all solutions. The adsorbent followed the monolayer-Langmuir isotherm for N ions and the multilayer-Freundlich isotherm for P, indicating efficient adsorption processes. Thermodynamic experiments indicated that the adsorption of P and N was not only feasible but also occurred spontaneously in a natural manner. This study revealed that the strategic modification of biochar plays a crucial role in advancing effective wastewater treatment technologies designed for nutrient removal.

Selective production of phenolic monomer via catalytic depolymerization of lignin over cobalt-nickel-zirconium dioxide catalyst.

The utilization of lignin, an abundant and renewable bio-aromatic source, is of significant importance. In this study, lignin oxidation was examined at different temperatures with zirconium oxide (ZrO2)-supported nickel (Ni), cobalt (Co) and bimetallic Ni-Co metal catalysts under different solvents and oxygen pressure. Non-catalytic oxidation reaction produced maximum bio-oil (35.3 wt%), while catalytic oxidation significantly increased the bio-oil yield. The bimetallic catalyst Ni-Co/ZrO2 produced the highest bio-oil yield (67.4 wt%) compared to the monometallic catalyst Ni/ZrO2 (59.3 wt%) and Co/ZrO2 (54.0 wt%). The selectively higher percentage of vanillin, 2-methoxy phenol, acetovanillone, acetosyringone and vanillic acid compounds are found in the catalytic bio-oil. Moreover, it has been observed that the bimetallic Co-Ni/ZrO2 produced a higher amount of vanillin (43.7% and 13.30 wt%) compound. These results demonstrate that the bimetallic Ni-Co/ZrO2 catalyst promotes the selective cleavage of the ether ß-O-4 bond in lignin, leading to a higher yield of phenolic monomer compounds.

Thermochemical Characterization and Kinetics of Biomass, Municipal Plastic Waste, and Coal Blends and Their Potential for Energy Generation via Gasification.

Feedstocks such as coal, biomass, plastics, and their blends have the potential to serve as fuels for the thermochemical conversion process owing to their relatively high calorific values. Nevertheless, the relative proportion of these feedstock blends has a pivotal influence over the overall energy conversion efficiency. Consequently, conducting a comprehensive study to optimize the blend proportion becomes crucial in order to obtain an optimal fuel. The study aims to investigate the thermochemical characterization and kinetics of blends composed of lignite coal, southern pine biomass, and municipal waste plastic blend to optimize the blend proportion. This optimization has been achieved through an analysis of 12 distinct blends, considering factors such as combustion reaction kinetics, combustion stability, and comprehensive combustion indices. The reaction kinetics, including activation energy, pre-exponential factor, and reaction order, were estimated using various methods, including Vyazovkin, Kissinger-Akahira-Sunose, Flynn-Wall-Ozawa, Master-plot, and multidistributed activation energy methods. The investigation revealed that increasing the biomass content within the blends enhances both the combustion stability and combustion performance. The multidistributed activation energy model exhibited a good fit with both the experimental thermogravimetric and the derivative thermogravimetric curves, achieving linear regression fitness values of 0.99 and 0.95, respectively. To showcase the viability of these blends as energy generation feedstock, the optimal blend comprised of 60% biomass, 10% coal, and 30% municipal waste plastic blend, possessing the lowest activation energy (110 kJ/mol), was employed as the feedstock for the fluidized bed oxy-steam gasification process. The gasification process resulted in a synthetic gas consisting of 47.79 mol % H2, 27.96 mol % CO, 5.85 mol % CH4, and 18.38 mol % CO2 (nitrogen-free basis) with a cold gas efficiency of 72.88%. The findings of this study can offer valuable insights into global industries engaged in the thermochemical conversion of solid waste materials.

Phosphorus adsorption using chemical and metal chloride activated biochars: Isotherms, kinetics and mechanism study.

Efficient treatment of nutrient-rich wastewater is of paramount importance for protecting the ecosystem. In this work, an efficient, abundant, and eco-friendly adsorbent was derived from biochar and employed for phosphorus (P) adsorption. The key factors influencing the P removal efficiency of the activated biochar, including P concentration, pH, dosage, temperature, adsorption time, and influence of co-existing ion type, were investigated. Maximum P adsorption percentage (100%) was obtained with 10 mg/L and zinc chloride activated biochar (BC-Zn) compared to the other activated biochars. Results show that by increasing the P concentration from 5 to 200 mg/L, the phosphorus adsorption capacity increases from 0.13 to 10.4 mg/g biochar. Isotherms and kinetic studies further show that the P adsorption follows the Langmuir and quasi-second-order kinetic models. The mechanistic investigation demonstrated that P adsorption occurred by precipitation reaction. Furthermore, P desorption has been studied at different time intervals to understand the P release rate after adsorption.

Mechanistic understanding of perfluorooctane sulfonate (PFOS) sorption by biochars.

Biochar has recently emerged as a cost-effective solution to combat per- and polyfluoroalkyl substances (PFAS) pollution in water, but mechanistic understanding of which physicochemical properties of biochars dictate PFAS sorptive removal from water remains elusive. Herein, 15 biochars were pyrolyzed from five feedstocks (corn, Douglas fir, eucalyptus, poplar, and switchgrass) at three pyrolysis temperatures (500, 700, and 900 °C) to investigate their removal efficiencies and mechanisms of perfluorooctane sulfonate (PFOS) from water. A commercial biochar was also included for comparison. Biochar physiochemical properties, including elemental composition, pH, specific surface area (SSA), pore structure, hydrophobicity, surface charge, surface functional groups, and crystalline structure were systematically characterized. Batch sorption data showed that the Douglas fir 900 biochar (Douglas fir and 900 are the feedstock type and pyrolysis temperature, respectively; this naming rule applies to other biochars), poplar 900 biochar, and commercial biochar can remove over 95% of PFOS from water. Structural equation model (SEM) was used to elucidate which biochar properties affect PFOS sorption. Interestingly, biochar pore diameter was identified as the most critical factor controlling PFOS removal, but pore diameter/pore volume ratio, SSA, pyrolysis temperature, hydrophobicity, and elemental composition all played variable roles. Hypothetically, biochars with small pore diameters and large pore volumes had a narrow yet deep pore structure that traps PFOS molecules inside once already sorbed, resulting in an enhanced PFOS sorption. Biochars with small pore diameter, low nitrogen content, and high pyrolysis temperature were also favorable for enhanced PFOS sorption. Our findings advance the knowledge of using biochars with optimized properties to remove PFOS and possibly other similar PFAS compounds from water.

Determination of level of self-reported adherence of antihypertensive drug(s) and its associated factors among patient with hypertension at a tertiary care center.

The study aimed to determine the level of self-reported adherence to antihypertensive drug(s) and its associated factors among patient with hypertension at a tertiary care center. The authors performed hospital based observational cross-sectional study using semi-structured questionnaires, WHO STEP tool and Hill and Bone high blood pressure compliance scale from December 1, 2021 to February 28, 2022. Descriptive statistics, Chi-square/Fisher's exact test and non-parametric tests were used for statistical analysis. Among 150 cases included in the study, majority (94, 62.67%) had good adherence based on Hill and Bone high blood pressure compliance scale with adherence level labelled as "good adherence" (score 3) and "not good adherence" (score < 3). The adherence to drug therapy was significantly better in females compared to males (50 [71.43%] vs. 44 [55.00%], p = .038). Among the factors related to hypertension and anti-hypertensive therapy, people with higher body mass index (ρ = -.324, n = 56, p = .015) and taking three or more pills (6, 1.71%, p = .017) had lower adherence to therapy. Likewise, forgetfulness (30, 53.57%), ineffective counseling (7, 12.50%), and missed follow-up (13, 23.21%) were the factors associated with lower adherence to anti-hypertensive therapy. This study finds good adherence among the patients taking anti-hypertensive medications. However, with the improved education, lesser number of pills and physical fitness help to adhere with the anti-hypertensive therapy.

Fast Pyrolysis Bio-Oil-Based Epoxy as an Adhesive in Oriented Strand Board Production.

The objectives of this study were to utilize bio-oil-based epoxy resin in oriented strand board (OSB) production and investigate the effect of bio-oil substitution in epoxy resin as an adhesive for OSB production. Bio-oil was produced by the fast pyrolysis (FP) process using southern yellow pine (Pinus spp.). Bio-oil-based epoxy resin was synthesized by the modification of epoxy resin with FP bio-oil at various substitution levels. Acetone extraction using a Soxhlet process indicated a superior cured reaction of bio-oil and epoxy resin at 20% bio-oil substitution. FTIR spectra corroborated the Soxhlet extraction with the removal of the epoxide peak signature within the cross-linked polymer. Images from the scanning electron microscopy suggested bulk phase homogeneity. OSB panels were tested according to ASTM D1037-12. The modulus of rupture (MOR), modulus of elasticity (MOE), internal bond strength, and water resistance (thickness swell and water absorption) properties of the OSB panels were feasible at bio-oil substitution up to 30% in the epoxy resin system.

Sorption and recovery of phenolic compounds from aqueous phase of sewage sludge hydrothermal liquefaction using bio-char.

Bio-char, a by-product of thermochemical conversion processes, has a great potential in phenolic compounds sorption from the waste aqueous phase produced from the hydrothermal liquefaction (HTL) process while being a low-cost sorbent. This study investigated the effect of temperature, pH, bio-char concentration, and mixing speed on two types of bio-char sorption of phenolic compounds using Taguchi's design of experiment and response surface method. Isothermal kinetics and thermodynamic properties were also evaluated to explain the sorption mechanism. The experimental results were well described by the pseudo-second-order kinetic model for both types of bio-char. The Langmuir isotherm model was found to be more suitable at high sorption temperatures, while the Freundlich isotherm model was better at low temperatures. Finally, the alkaline desorption and regeneration experiments were examined, and the eluents with phenolic compounds were characterized using a liquid chromatography-mass spectrometer.

Effect of ammonia removal and biochar detoxification on anaerobic digestion of aqueous phase from municipal sludge hydrothermal liquefaction.

Hydrothermal liquefaction is a promising method to convert municipal sludge into an energy-dense fuel. The inevitable by-product aqueous phase is rich in complex organics, which has the potential for energy and nutrient recovery and can be treated by anaerobic digestion to produce methane. However, toxic compounds such as ammonia and phenolics present would inhibit the function of micro-organisms. This study investigated the influence of ammonia and phenolics removal on anaerobic digestion. The results showed that the treated aqueous phase resulted in up to 225 ml CH4/g COD. The highest methane production was obtained in the culture with both ammonia and phenolics removal at pH 7.0, which was about 90% higher than only ammonia removal and seven times higher than only phenolics removal. The microbial community analysis results showed that these two treatments could increase microbial diversity and upregulate the relative abundance of methanogens.

Use of Biomaterials for 3D Printing by Fused Deposition Modeling Technique: A Review.

Three-dimensional (3D) printing is a revolutionary manufacturing technique that can fabricate a 3D object by depositing materials layer by layer. Different materials such as metals, polymers, and concretes are generally used for 3D printing. In order to make 3D printing sustainable, researchers are working on the use of different bioderived materials for 3D printing. Because of the abundant and sustainable sources, and versatile properties, biomaterials are considered as the potential candidates that have the ability to replace petroleum-based polymers. This review highlights the basic overview of fused deposition modeling (FDM) technique of 3D printing and recent developments that have occurred on FDM printing using biomaterials. Specifically, FDM printing process, final properties, and characteristics of biopolymers, their composites, and polymers containing biofillers are discussed.

Enhancement of biogas production from wastewater sludge via anaerobic digestion assisted with biochar amendment.

Studies have shown that biochar enhances methane formation due to the presence of redox active moieties and its conductive properties. This study investigated the influence of biochar, which was produced from Douglas fir pyrolysis, on biogas production and microbial community during anaerobic digestion (AD) of wastewater sludge. The results showed that biochar significantly enhances methane (CH4) production rate and increases its final yield during AD. The cumulative highest CH4 production obtaining in cultures with DF500 (biochar from Douglas fir at 500 °C) were about 11% and 98% more than the culture without biochar at 37 °C and 25 °C AD temperature, respectively. At 55 °C, the maximum CH4 yield reached 172.3 ml/g COD with DF730, which was about 48.3% more than control culture. The microbial community analysis results showed that biochar could up-regulate the role of micro-ecology especially the methanogens and improve the AD process.

Hydrogen production via thermocatalytic decomposition of methane using carbon-based catalysts.

Thermocatalytic decomposition (TCD) of methane is one of the most effective methods for pure hydrogen production. Catalysts were selected for TCD of methane in this study to utilize biochar as a catalyst. Among these catalysts, two catalysts (named activated biochar (AB) and heat-treated biochar (HB)) were prepared from Douglas fir, whereas the other four were prepared using commercial activated carbon and zeolite with and without doping ruthenium metal. The catalysts were characterized using XRD, SEM imaging, TEM, H2-TPR, and BET specific surface area and pore size analysis. The Ru doped commercial activated carbon catalyst (Ru-AC) was deactivated continuously during a 60 h reaction run, whereas AB exhibited comparatively stable methane conversion up to 60 h. The methane conversion was 21% for Ru-AC and 51% for AB after 60 h of reaction time at 800 °C. The very high surface area of AB (∼3250 m2 g-1) and its microporosity compared to other catalysts could have resulted in resistance against rapid deactivation. Furthermore, carbon nanotube by-products were observed in TEM images of solid residues that could form due to the presence of alkali metals in the biochar. Carbon nanotube formation could contribute significantly to the extended life of AB.

Leaching and anaerobic digestion of poultry litter for biogas production and nutrient transformation.

Anaerobic digestion of poultry litter is a potentially sustainable means of stabilizing this waste while generating biogas. However, technical challenges remain including seasonality of litter production, low C/N ratios, limited digestibility of bedding, and questions about transformation of nutrients during digestion. This study investigated biogas production and nutrient transformations during anaerobic digestion of poultry litter leachate and whole litter. Use of fresh litter collected from within the house was also compared to waste litter cake that was stored outdoors on the farm. The results showed that litter leachates had higher biomethane potential (0.24-0.30 L/gVS) than whole litter (0.15-0.16 L/gVS) and the insoluble bedding material left after leaching (0.08-0.13 L/gVS). Leachates prepared from waste litter cake had lower uric acid and higher acetic acid concentrations than fresh litter indicating that decomposition had occurred during storage. Consequently, waste litter cake had faster initial biogas production but lower final biogas yields compared to fresh litter. In all reactors, uric and acetic acids were completely consumed during digestion, phosphate levels decreased but ammonium levels increased. The results demonstrate that poultry litter leachate is amenable to digestion despite a low C/N ratio and that the remaining insoluble bedding material has been partially stripped of its nutrients. Moreover, litter can be stored prior to digestion but some losses in biomethane potential should be expected due to decomposition of organics during storage.

Co-pyrolysis of lignin and plastics using red clay as catalyst in a micro-pyrolyzer.

In the current study, low-density polyethylene and polystyrene were co-pyrolyzed with dealkaline lignin in a micro-reactor at 500 °C with and without low-cost red clay catalyst. The products were analyzed with GC-MS/FID to quantify phenolic compounds, alkanes and alkenes. The synergistic effect between plastics and lignin was studied by comparing the carbon yield of compounds from co-pyrolysis with that from individual pyrolysis. The co-pyrolysis of lignin and polystyrene was also performed at 600, 700 and 800 °C to examine the effect of pyrolysis temperature. The study explores a novel approach to enhance lignin depolymerization with red clay catalyst while utilizing waste plastics.

Detoxification of Organosolv-Pretreated Pine Prehydrolysates with Anion Resin and Cysteine for Butanol Fermentation.

Bioconversion of lignocellulose to biofuels suffers from the degradation compounds formed during pretreatment and acid hydrolysis. In order to achieve an efficient biomass to biofuel conversion, detoxification is often required before enzymatic hydrolysis and microbial fermentation. Prehydrolysates from ethanol organosolv-pretreated pine wood were used as substrates in butanol fermentation in this study. Six detoxification approaches were studied and compared, including overliming, anion exchange resin, nonionic resin, laccase, activated carbon, and cysteine. It was observed that detoxification by anion exchange resin was the most effective method. The final butanol yield after anion exchange resin treatment was comparable to the control group, but the fermentation was delayed for 72 h. The addition of Ca(OH)2 was found to alleviate this delay and improve the fermentation efficiency. The combination of Ca(OH)2 and anion exchange resin resulted in completion of fermentation within 72 h and acetone-butanol-ethanol (ABE) production of 11.11 g/L, corresponding to a yield of 0.21 g/g sugar. The cysteine detoxification also resulted in good detoxification performance, but promoted fermentation towards acid production (8.90 g/L). The effect of salt on ABE fermentation was assessed and the possible role of Ca(OH)2 was to remove the salts in the prehydrolysates by precipitation.

Catalytic upgrading of bio-oil produced from hydrothermal liquefaction of Nannochloropsis sp.

Upgrading of bio-oil obtained from hydrothermal liquefaction (HTL) of algae is necessary for it to be used as a fuel. In this study, bio-oil obtained from HTL of Nannochloropsis sp. was upgraded using five different catalysts (Ni/C, ZSM-5, Ni/ZSM-5, Ru/C and Pt/C) at 300 °C and 350 °C. The upgraded bio-oil yields were higher at 300 °C; however, higher quality upgraded bio-oils were obtained at 350 °C. Ni/C gave the maximum upgraded bio-oil yield (61 wt%) at 350 °C. However, noble metal catalysts (Ru/C and Pt/C) gave the better upgraded bio-oils in terms of acidity, heating values, and nitrogen values. The higher heating value of the upgraded bio-oils ranged from 40 to 44 MJ/kg, and the nitrogen content decreased from 5.37 to 1.29 wt%. Most of the upgraded bio-oils (35-40 wt%) were in the diesel range. The major components present in the gaseous products were CH4, CO, CO2 and lower alkanes.

Decentralized biorefinery for lignocellulosic biomass: Integrating anaerobic digestion with thermochemical conversion.

Anaerobic digestion (AD) of lignocellulosic biomass i.e. Napier grass (Pennisetum purpureum), was investigated via a series of batch and bench-scale experiments. Two semi-continuous bench-scale horizontal bioreactors were operated in parallel for nearly 300 days, and the reactors were able to handle the organic loading rate (OLR) up to 6 kg volatile solids (VS)/m3-d, which was among the highest OLR reported in the literature for lignocellulosic biomass. Hemicellulose was the main structural carbohydrate of lignocellulosic biomass per unit respective mass (dry weight) basis contributing to methane production. The cellulose- and lignin-rich digestate was further examined for its bioenergy potential via torrefaction and hydrothermal carbonization, and was found to have higher mass and energy yield compared with those of raw Napier grass. The produced solid char has energy content similar to bituminous coal with low ash content. Thus, this study provided a successful integration of anaerobic digestion with thermochemical conversion representing a biorefinery concept for lignocellulosic feedstocks.

Environmental application of biochar: Current status and perspectives.

In recent years, there has been a significant interest on biochar for various environmental applications, e.g., pollutants removal, carbon sequestration, and soil amelioration. Biochar has several unique properties, which makes it an efficient, cost-effective and environmentally-friendly material for diverse contaminants removal. The variability in physicochemical properties (e.g., surface area, microporosity, and pH) provides an avenue for biochar to maximize its efficacy to targeted applications. This review aims to highlight the vital role of surface architecture of biochar in different environmental applications. Particularly, it provides a critical review of current research updates related to the pollutants interaction with surface functional groups of biochars and the effect of the parameters variability on biochar attributes pertinent to specific pollutants removal, involved mechanisms, and competence for these removals. Moreover, future research directions of biochar research are also discussed.