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.

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.

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.

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.