Increasing Pyrolysis Temperature Research Articles

Tetracycline (TC) removal from wastewater with activated carbon (AC) obtained from waste grape marc: activated carbon characterization and adsorption mechanism.

In this study, activated carbons were obtained from grape marc for tetracycline removal from wastewater. Activated carbons were obtained by subjecting them to pyrolysis at 300, 500, and 700°C, respectively, and the effect of pyrolysis temperature on activated carbons was investigated. The physicochemical and surface properties of the activated carbons were evaluated by SEM, FTIR, XRD, elemental analysis, N2 adsorption/desorption isothermal, thermal gravimetric (TG) and derivative thermogravimetric (DTG), and BET surface area analysis. When the BET surface areas were examined, it was found that 4.25 m2/g for activated carbon was produced at 300°C, 44.23 m2/g for activated carbon obtained at 500°C and 44.23 m2/g at 700°C, which showed that the BET surface areas increased with increasing pyrolysis temperatures. The pore volumes of the synthesized activated carbons were 0.0037 cm3/g, 0.023 cm3/g, and 0.305 cm3/g for pyrolysis temperatures of 300, 500, and 700°C, respectively, while the average pore size was found to be 8.02nm, 9.45nm, and 10.29nm, respectively. A better adsorption capacity was observed due to the decrease in oxygen-rich functional groups with increasing pyrolysis temperature. It was observed that the activated carbon obtained from grape skins can easily treat hazardous wastewater containing tetracycline due to its high carbon content and surface functional groups. It was also shown that the activated carbon synthesized in this study has a higher pore volume despite its low surface area compared to the studies in the literature. Thanks to the high pore volume and surface active groups, a successful tetracycline removal was achieved.

Enhanced catalytic activity of Sm/CeO2 to produce gasoline-range hydrocarbons from pyrolysis of spent coffee grounds

This study investigated the application of Sm/CeO2 catalyst for hydrocarbon production in catalytic pyrolysis (CP) of spent coffee grounds (SCGs). A temperature range of 450-750 °C and catalyst/biomass (C/B) ratios of 0.5-4 were employed in the CP. The results showed that an increase in pyrolysis temperature consistently increased the quantity of hydrocarbons and considerably decreased the oxygenated compounds like acids and phenols. At temperatures of 450 and 550 °C, C/B ratios of 2 or 1 generated the maximum amount of hydrocarbons. At 650 and 750 °C temperatures, C/B ratios of 0.5 and 1 were capable to achieve a higher content of hydrocarbons in bio-oils, suggesting the synergistic effect of temperature and catalyst activity. The hydrocarbons in bio-oils were found in the gasoline range, mainly containing benzene, toluene, ethylbenzene, xylene (BTEX), olefins, and cycloalkenes. Primary reactions involved to convert oxygenated compounds into hydrocarbons were dehydration, decarboxylation, decarbonylation, dehydrogenation, isomerization, and aromatization reactions.

Rheological evaluation of paving asphalt binder containing bio-oil from rice straw pyrolysis

The conversion of rice straw to bio-oil for substituting asphalt paving materials not only contributes to sustainable development in construction industry, but is also beneficial for resource recovery in agriculture. In this study, rice straw was pyrolyzed to produce bio-oil by using fluidized bed, and the influences of key pyrolysis conditions on product distribution were investigated. Bio-asphalt was prepared by high-speed mixing of pyrolysis bio-oil and petroleum asphalt, and comprehensively evaluated through rheological tests and continuous grading of performance grade (PG). Moreover, microscopic characterization was conducted to further explore the mechanism of bio-oil modification of asphalt. The test results indicate that the yield of bio-oil first rises and then drops with the increase of pyrolysis temperature. As the gas flow rate increases and the biomass particle size decreases, the bio-oil yield shows an increasing trend. The bio-asphalt containing bio-oil from lower pyrolysis temperatures has stronger rutting resistance and lower temperature susceptibility. As the pyrolysis temperature rises, the resistances of bio-asphalt to fatigue and thermal cracking are enhanced. According to continuous PG grading, the widest safe working temperature range is obtained at 450 ℃. Compared to base asphalt, bio-asphalt has superior fatigue and low-temperature performances at high pyrolysis temperatures. Additionally, it can be known from Fourier transform infrared spectroscopy that the modification of petroleum asphalt by bio-oil is a physical fusion process.

CPD model prediction of oil sand pyrolysis based on structural parameters from 13C NMR and FTIR measurements

Here, carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) and Fourier transform infrared spectroscopy (FTIR) techniques were used to study the chemical structure characteristics of oil sand and its pyrolysis oil. The FTIR results showed that the values of the CH2/CH3 ratio, A-factor, and DOC1 of the pyrolysis oil decreased during the pyrolysis process, while the C-factor showed a maximum value with increasing pyrolysis temperature. The 13C NMR results showed that methylides and methylides were mainly contributed to oil production. The aliphatic chain in the pyrolysis oil has little alterations during pyrolysis, while the extent of aromatic ring substitution increases from 0.46 to 0.58. Furthermore, a correlation was obtained between the chemical structure of oil and the pyrolysis product yields of oil sand. Moreover, using chemical structure parameters investigated with FTIR and 13C NMR and kinetic parameters based on the thermogravimetric data, the chemical percolation devolatilization (CPD) model was applied to simulate the pyrolysis of oil sand. The results showed that the simulated results for tar and light gas were in good agreement with the experimental data, while those for char underpredicted the experimental data. Overall, the CPD model can effectively predict the pyrolysis of oil sand.

Biochar aided priming of carbon and nutrient availability in three soil orders of India

In recent years biochar (BC) has gained importance for its huge carbon (C) sequestration potential and positive effects on various soil functions. However, there is a paucity of information on the long-term impact of BC on the priming effect and nutrient availability in soil with different properties. This study investigates the effects of BC prepared from rice husk (RBC4, RBC6), sugarcane bagasse (SBC4, SBC6) and mustard stalk (MBC4, MBC6) at 400 and 600 °C on soil C priming and nitrogen (N), phosphorus (P), and potassium (K) availability in an Alfisol, Inceptisol, and Mollisol. BC properties were analyzed, and its decomposition in three soil orders was studied for 290 days in an incubation experiment. Post-incubation, available N, P, and K in soil were estimated. CO2 evolution from BC and soil alone was also studied to determine the direction of priming effect on native soil C. Increasing pyrolysis temperature enhanced pH and EC of most of the BC. The pyrolysis temperature did not show clear trend with respect to priming effect and nutrient availability across feedstock and soil type. MBC6 increased C mineralization in all the soil orders while RBC6 in Alfisol and SBC6 in both Inceptisol and Mollisol demonstrated high negative priming, making them potential amendments for preserving native soil C. Most of the BC showed negative priming of native SOC in long run (290 days) but all these BC enhanced the available N, P, and K in soil. SBC4 enhanced N availability in Alfisol and Inceptisol, RBC4 improved N and P availability in Mollisol and P in Alfisol and MBC6 increased K availability in all the soils. Thus, based on management goals, tailored BC or blending different BC can efficiently improve C sequestration and boost soil fertility.

Empirical Correlation between Electrical Conductivity and Nitrogen Content in Biochar as Influenced by Pyrolysis Temperature

Much progress has been made in understanding the conditions of biochar production related to biochar properties and carbon (C). Still, very little knowledge has been gained regarding the effects on nitrogen (N), one of the most critical nutrients affected by pyrolysis temperature (PT). Analysis of N in biochar is costly, and alternative methods should be developed to estimate the N content in biochar quickly under different pyrolysis conditions. We hypothesized that there was a correlation between biochar N content and its electrical conductivity (EC). We aimed to evaluate total N and the effect of PT through the correlation with EC, a parameter that can be easily measured. Biochar products derived from coffee husk (CH) and chicken manure (CM) produced at increasing PT (300 to 750 °C) were used for the study and measured for total N and EC. The increase in PT caused significant N loss, consequently reducing total N content in biochars, with the highest loss (82%) and lowest total N content (1.2 g kg−1) found in CM biochar pyrolyzed at 750 °C. The lowest N loss (21% for CH biochar and 36% for CM biochar) was observed at a PT of 300 °C. A negative correlation between EC and total N and a positive correlation with N loss were found in both biochar products across the wide range of PT investigated. To preserve the N content in biochars, the PT should not exceed 400 °C. Our results indicate that EC is a fast and accurate biochar proxy attribute capable of predicting the N content and its loss in coffee husk and chicken manure-derived biochars as the pyrolysis temperature increased from 300 °C to 750 °C and could be used as an alternative to predict the N in biochar easily. A more extensive set of biochar samples and pyrolysis conditions should be tested to validate this approach.

Untapped potential of food waste derived biochar for the removal of heavy metals from wastewater

The presence of heavy metals in water pose a serious threat to both public and environmental health. However, the advances in the application of low cost biochar based adsorbent synthesize from various feedstocks plays an effective role in the of removal heavy metals from water. This study implies the introduction of novel method of converting food waste (FW) to biochar through pyrolysis, examine its physiochemical characteristics, and investigate its adsorption potential for the removal of heavy metals from water. The results revealed that biochar yield decreased from 18.4 % to 14.31 % with increase in pyrolysis temperature from 350 to 550 °C. Likewise, increase in the pyrolysis temperature also resulted in the increase in the ash content from 39.87 % to 42.05 % thus transforming the biochar into alkaline nature (pH 10.17). The structural and chemical compositions of biochar produced at various temperatures (350, 450, and 550 °C) showed a wide range of mineralogical composition, and changes in the concentration of surface functional groups. Similarly, the adsorption potential showed that all the produced biochar effectively removed the selected heavy metals from wastewater. However a slightly high removal capacity was observed for biochar produced at 550 °C that was credited to the alkaline nature, negatively charged biochar active sites due to O-containing functional groups and swelling behavior. The results also showed that the maximum adsorption was recorded at pH 8 at adsorbent dose of 2.5 g L−1 with the contact time of 120 min. To express the adsorption equilibrium, the results were subjected to Langmuir and Freundlich isotherms and correlation coefficient implies that the adsorption process follows the Freundlich adsorption isotherm. The findings of this study suggest the suitability of the novel FW derived biochar as an effective and low cost adsorbent for the removal of heavy metals form wastewater.

Heteroatoms-doped hierarchically porous graphene as electrode material for supercapacitors with ultra-high capacitance

In this work, a dual-templating pyrolysis strategy is successfully developed to synthesize a highly crumpled graphene (N-TRPG-800). The achievement of the graphene is based on the carbonization of the d(+)-glucosamine hydrochloride and the spatial confinement effect of the graphitic carbon nitride (g-C3N4) in the presence of zinc nanoparticles (Zn NPs). During the pyrolysis process, the d(+)-glucosamine hydrochloride first polymerizes into the layers of g-C3N4, which is derived from melamine. Afterwards, a further increase in pyrolysis temperature leads to the decomposition of g-C3N4 and the generation of reducing NH3 gas, which eventually resulting in the formation of 2D ultrathin structure and high heteroatoms doping degree. Simultaneously, the volatilization of the Zn NPs also plays a key role in the pore formation and the hierarchical structure generation. As a result, the as-synthesized graphene sheets simultaneously possesses hierarchical porous structure, high heteroatoms-doped degree, and large specific surface area (506 m2 g−1). Electrochemical measurements show that the N-TRPG-800 exhibits an ultrahigh supercapacitance of 471 F g−1 at 0.2 A g−1 in a three-electrode mode, approaching the theoretical capacitance of 550 F g−1 of graphene, which is superior to that of the state-of-the-art heteroatom-doped porous carbons in literature.

Effect of pyrolysis temperature and molecular weight on characterization of biochar derived dissolved organic matter from invasive plant and binding behavior with the selected pharmaceuticals

A comprehensive understanding of the characteristics of biochar released-dissolved organic matter (BDOM) derived from an invasive plant and its impact on the binding behavior of pharmaceuticals is essential for the application of biochar, yet has received less attention. In this study, the binding behavior of BDOM pyrolyzed at 300–700 °C with sulfathiazole, acetaminophen, chloramphenicol (CAP), and carbamazepine (CMZ) was investigated based on a multi-analytical approach. Generally, the pyrolysis temperature exhibited a more significant impact on the spectral properties of BDOM and pharmaceutical binding behavior than those of the molecular weight. With increased pyrolysis temperature, the dissolved organic carbon decreased while the proportion of the protein-like substance increased. The highest binding capacity towards the drugs was observed for the BDOM pyrolyzed at 500 °C with the molecular weight larger than 0.3 kDa. Moreover, the protein-like substance exhibited higher susceptive and released preferentially during the dialysis process and also showed more sensitivity and bound precedingly with the pharmaceuticals. The active binding points were the aliphatic C–OH, amide II N–H, carboxyl CO, and phenolic-OH on the tryptophan-like substance. Furthermore, the binding affinity of the BDOM pyrolyzed at 500 °C was relatively high with the stability constant (logKM) of 4.51 ± 0.52.

Application of Infrared Pyrolysis and Chemical Post-Activation in the Conversion of Polyethylene Terephthalate Waste into Porous Carbons for Water Purification.

In this study, we compared the conversion of polyethylene terephthalate (PET) into porous carbons for water purification using pyrolysis and post-activation with KOH. Pyrolysis was conducted at 400-850 °C, followed by KOH activation at 850 °C for samples pyrolyzed at 400, 650, and 850 °C. Both pyrolyzed and post-activated carbons showed high specific surface areas, up to 504.2 and 617.7 m2 g-1, respectively. As the pyrolysis temperature increases, the crystallite size of the graphite phase rises simultaneously with a decrease in specific surface area. This phenomenon significantly influences the final specific surface area values of the activated samples. Despite their relatively high specific surface areas, pyrolyzed PET-derived carbons prove unsuitable as adsorbents for purifying aqueous media from methylene blue dye. A sample pyrolyzed at 650 °C, with a surface area of 504.2 m2 g-1, exhibited a maximum adsorption value of only 20.4 mg g-1. We propose that the pyrolyzed samples have a surface coating of amorphous carbon poor in oxygen groups, impeding the diffusion of dye molecules. Conversely, post-activated samples emerge as promising adsorbents, exhibiting a maximum adsorption capacity of up to 127.7 mg g-1. This suggests their potential for efficient dye removal in water purification applications.

Physicochemical, thermodynamic, and kinetic controls on volatile products, bio-oils, and biochars of Lycium barbarum pyrolysis and their multi-objective optimization

The substantial stream of Lycium barbarum (LBL) residues presents an opportunity for the valorized generation of energy and products through their pyrolysis. This study aimed to quantify the pyrolytic bioenergy potential of LBL by assessing its physicochemical properties, pyrolysis performance, kinetics, thermodynamics, volatile products, bio-oils, and biochars. The LBL pyrolysis consisted of the three consecutive stages of dehydration, devolatilization, and charring or carbonization of the residuals. The main pyrolysis temperature varied between 125.00 and 700.00 °C. The kinetic and thermodynamic parameters of the LBL pyrolysis (0.1 < α < 0.9) were estimated via the Friedman method. Its activation energy ranged from 133.10 to 318.36 kJ/mol. Gases and functional groups identified included H2O, CO2, CH4, CO, CC, C-O, and C-OH. The primary pyrolytic outputs comprised ketones/alcohols, furans, acids, and N-containing compounds. Artificial neural networks were employed to jointly reconstruct and optimize the pyrolysis conditions. The simultaneously minimum gas emissions occurred at 677 and 1000 °C. The temperature dependence of pyrolytic biochar production was also characterized. The formation of pores was attributed to the increased pyrolysis temperature, increasing both the release of volatiles and the carbonization degree of activated carbon. This study provides both theoretical insights and practical guidance for the comprehensive utilization and effective management of Lycium barbarum residues.

Insights into pyrolysis process of coconut shell waste hydrochar: In-situ structural evolution and reaction kinetics

Coconut shell (CS) can be efficiently utilized by coupling hydrothermal carbonization (HTC) pretreatment with pyrolysis to meet the goal of global green development. In-situ Raman spectroscopy and thermogravimetric analyzer (TGA) were adopted to investigate the structural evolutions and reaction kinetics characteristics of hydrochar during the pyrolysis process. According to the results, the intensity of peak D and peak G in Raman spectrum decreased with increasing hydrothermal degree. Mild HTC treatment (≤200 °C) led to an increase in ID/IG, indicating the formation of large aromatic rings through small ring condensation. In contrast, severe HTC treatment (≥220 °C) reduced the ID/IG ratio, indicating an increased polycondensation of aromatic compounds and a higher degree of aromatization, resulting in larger molecules sizes. The spectral area below 400 °C reduced with increasing pyrolysis temperature due to the reduction of oxygen-containing functional groups and thermal radiation. Above 400 °C, the total area remains stable as the Raman spectrum scattering ability increases due to char formation and aromatization reactions. HTC-200 exhibited an increase in ID/IG from 0.54 to 0.72 and ID/I(Me + Ke + GL) from 0.58 to 0.68 with increasing pyrolysis temperatures. The activation energy during pyrolysis ranged from 194.50 to 238.34 kJ/mol for CS and 217.51–259.51 kJ/mol for HTC-200. Hydrothermal carbonization had a significant effect on pyrolysis behavior of hydrochar, as it was found that the mild HTC hydrochar followed D-type diffusion models when conversion rate was less than 0.65, and transitioned to higher reaction order in the late-stage of pyrolysis.

A new approach to explore and assess the sustainable remediation of chromium-contaminated wastewater by biochar based on 3E model

As a cost-effective material, biochar, known as ‘black gold’, has been widely used for environmental applications (EA), including chromium-contaminated wastewater remediation. However, limited reports focused on the multiple impacts of biochar, including energy consumption (EC) and environmental risk (ER). Hence, to recommend biochar as a green material for sustainable development, the three critical units were explored and quantitatively assessed based on an adapted 3E model (EA-EC-ER). The tested biochar was produced by limited-oxygen pyrolysis at 400–700 °C by using three typical biomasses (Ulva prolifera, phoenix tree, and municipal sludge), and the optimal operational modulus of the 3E model was identified using six key indicators. The findings revealed a significant positive correlation between EC and biochar yield (p < 0.05). The biochar produced by phoenix tree consumed more energy due to having higher content of unstable carbon fractions. Further, high-temperature and low-temperature biochar demonstrated different chromium removal mechanisms. Notably, the biochar produced at low temperature (400 °C) achieved better EA due to having high removal capacity and stability. Regarding ER, pyrolysis temperature of 500 °C could effectively stabilize the ecological risk in all biochar and the biochar produced by Ulva prolifera depicted the greatest reduction (37-fold). However, the increase in pyrolysis temperature would lead to an increase in global warming potential by nearly 22 times. Finally, the 3E model disclosed that the biochar produced by Ulva prolifera at 500 °C with low EC, high EA, and low ER had the most positive recommendation index (+78%). Importantly, a rapid assessment methodology was established by extracting parameters from the correlation. Based on this methodology, about eight percent of biochar can be the highest recommended from more than 100 collected peer-related data. Overall, the obtained findings highlighted that the multiple impacts of biochar should be considered to efficiently advance global sustainable development goals.

Oxidation Mechanism and Surface Characterization of Pyrolytic Graphite in Simulated Air for Pyrochemical Reprocessing Application

Accidental air ingress into the containment chamber of pyrochemical reprocessing of spent nuclear fuels can cause severe oxidation of graphite components. Pyrolytic graphite (PyG) coating on conventional high-density graphite (HDG) is proposed for protection against oxidation, molten salt, and molten metal corrosion. The aim of the present study is to evaluate the thermal stability and kinetic parameters and propose a suitable oxidation mechanism of PyG under simulated air using thermogravimetry analysis (TGA). In dynamic oxidation, a linear increase in the oxidation onset, peak, and burnout temperature is observed for PyG synthesized at increasing pyrolysis temperature from 1200 to 2400°C except for 1400°C. The isothermal oxidation study showed a similar trend i.e., a decrease in the linear oxidation rate constant value for any given isotherm with increasing pyrolysis. The Arrhenius plot showed two-stage oxidation regimes operating between 600 to 1000°C. In regime-I, between 600 to ∼800°C controlled by surface chemical reaction kinetics, the activation energy is measured between 100-200 kJ.mol−1. The graphite-oxygen reaction initiates and propagates preferentially along the prismatic planes at the sample edges, where the dangling bonds of stacked graphite layer structures are exposed. In regime-II operating above ∼800°C, the surface reaction rate is infinitely faster, and the diffusional mass transport becomes a rate-limiting factor. In this regime, the graphite-oxygen initiates by pore formation on defective reactive sites on the bulk surface and propagates by pore-widening and pore-coalescence mechanism. The observed differences in the oxidation rates for different pyrolysis PyG attributed to its intrinsic material properties are investigated. This work provides new insights into the oxidation mechanism of the PyG during accidental air ingress in a pyrochemical reprocessing plant.

Techno-economic and environmental analyses of the pyrolysis of food waste to produce bio-products

Food waste has become a source of concern as it is generated abundantly worldwide and needs to be valorised into new products. In this study, cucumber, tomato, and carrot wastes were investigated as pyrolysis feedstocks as a single component (cucumber), a binary component mixture (cucumber and tomato), and a ternary component blend (cucumber, tomato, and carrot). Fourteen scenarios were simulated and evaluated based on varying the feedstock blend (single, binary, and tertiary), temperature (300 and 500 °C), and feedstock moisture content (5, 20, and 40%). Using an established empirical model, the effect of these parameters on product yields, techno-economic implications, energy requirements, and life cycle analysis (LCA) outcomes were investigated. The best performers of each scenario were determined, and their strengths and weaknesses were identified and compared with other scenarios. In terms of product yields, all three systems (single, binary, and tertiary) followed a similar pattern: bio-oil yields increased as temperature and feedstock moisture content increased, while biochar yields decreased as temperature and feedstock moisture content increased. The production of syngas, on the other hand, was only observed at elevated temperatures. The total energy requirement exhibited an increase with increasing temperature and feedstock moisture content. The economic evaluation revealed that the return on investment (ROI) value for the single component at 5% moisture content at 300 °C is 29%, with a payback period (PB) of only 3.4 years, which is potentially very appealing. The water footprint increased with increasing pyrolysis temperature but decreased with increasing moisture content in all scenarios. The land footprint is observed to remain constant despite changes in process conditions. The study's findings contribute to the pyrolysis process's scalability, technological advancement, and commercialisation.

Pyrolysis characteristics and product distribution of oil sludge based on radiant heating.

It needs to be improved the conversion efficiency and stable operation of conventional pyrolysis with high-temperature flue gas heating (HFH). Herein, a new radiative heating (RH) pyrolysis method is proposed. Experimental studies are carried out on a self-made radiation pyrolysis pilot plant to investigate the effects of different factors (pyrolysis final temperature, residence time, and carrier gas volume) on product distribution. The results show that with the increase of pyrolysis temperature, the yield of the gas phase consistently increases, and the proportion of CH4 and H2 in the pyrolysis gas reaches 62.31% at 700°C. The yield of the liquid phase increases and then decreases. The recovery rate of pyrolysis oil achieves 68.07% when the pyrolysis temperature is 600°C with main components of ketones and unsaturated hydrocarbon compounds. The yield of the solid phase consistently decreases. The RH in this work generates more pyrolysis gas in the pyrolysis process and alleviates the effects of fouling layers on the continuous operation of the equipment which has guiding significance for the efficient resource utilization of oil sludge.

Role of biochar pyrolysis temperature on intracellular and extracellular biodegradation of biochar-adsorbed organic compounds

Immobilizing organic pollutants by adsorption of biochar in farmland soil is a cost-effective remediation method for contaminated soil. As the adsorption capacity of biochar is limited, biodegradation of biochar-adsorbed organic pollutants was a potential way to regenerate biochars and maintain the adsorption performance of biochars to lower the cost. It could be affected by the biochar pyrolysis temperature, but was not evaluated yet. In this study, biodegradation of adsorbed phenanthrene on a series of biochars with pyrolysis temperatures from 150 to 700 °C by Sphingobium yanoikuyae B1 was investigated using batch experiments of biodegradation kinetics at 30 °C, to explore the role of biochar pyrolysis temperature on biodegradation of biochar-adsorbed organic compounds. It was observed that 37.5–47.9% of adsorbed phenanthrene on moderate temperature-pyrolyzed biochars produced at 400 and 500 °C were biodegraded, less than that on high temperature-pyrolyzed biochars produced at ≥600 °C (48.8–60.8%) and low temperature-pyrolyzed biochars produced at ≤300 °C (63.4–92.5%). Phenanthrene adsorbed largely on the low temperature-pyrolyzed biochars by partition mechanism and thus is easily desorbed to water for a dominated intracellular biodegradation. On the high temperature-pyrolyzed biochars, phenanthrene is adsorbed largely by pore-filling mechanism and thus less desorbed to water for intracellular biodegradation. However, high temperature-pyrolyzed biochars can promote microbes to produce siderophore, H2O2 and thus release extracellular •OH for a dominated degradation of adsorbed phenanthrene by Fenton-like reaction. With the increase of biochar pyrolysis temperature, desorption and consequently the intracellular biodegradation of adsorbed phenanthrene on biochars decreased, while the secretion of siderophore and H2O2 by microbes on biochars increased to produce more extracellular •OH for degradation by Fenton-like reaction. The results could provide deep insights into the role of biochar pyrolysis temperature on biodegradation of biochar-adsorbed organic compounds, and optimize the selection of biochar with higher adsorption performance and easier regeneration for soil remediation.

Biochar derivation at low temperature: A novel strategy for harmful resource usage of antibiotic mycelial dreg

Antibiotic mycelial dreg (AMD) has been categorized as hazardous waste due to the high residual hazardous contaminants. Inappropriate management and disposal of AMD can cause potential environmental and ecological risks. In this study, the potential of pleuromutilin mycelial dreg (PMD) as a novel feedstock for preparing tetracycline hydrochloride (TC) adsorbent was explored to achieve safe management of PMD. The results suggested that residual hazardous contaminants were completely eliminated after pyrolysis. With the increase of pyrolysis temperature, the yields, H/C, O/C, (O + N)/C, and pore size in PMD-derived biochars (PMD-BCs) decreased, while BET surface area and pore volume increased, resulting in the higher stability of the PMD-BCs prepared from higher temperatures. The TC adsorption of the PMD-BCs increased from 27.3 to 46.9 mg/g with the increase of the pyrolysis temperature. Surprisingly, pH value had a strong impact on the TC adsorption, the adsorption capacity of BC-450 increased from 6.5 to 71.1 mg/g when the solution pH value increased from 2 to 10. Lewis acid-base interaction, pore filling, π-π interaction, hydrophobic interaction, and charge-assisted hydrogen bond (CAHB) are considered to drive the adsorption. This work provides a novel pathway for the concurrent detoxification and reutilization of AMD.

Pb(ΙΙ), Cd(ΙΙ), and Mn(ΙΙ) adsorption onto pruning-derived biochar: physicochemical characterization, modeling and application in real landfill leachate

The aim of this study was to systemically evaluate how different pyrolysis temperatures (400, 550, and 700 °C) and particle sizes (1–2 mm and 63–75 µm) were influenced biochar evolution, made from urban pruning waste, during pyrolysis process and to establish their relationships with biochar potential for removal of lead (Pb), cadmium (Cd), and manganese (Mn) from real municipal solid waste landfill leachate. The effects of pH (2–7), contact time (30–300 min) and adsorbent dosage (0.1–5 g L−1) on heavy metals removal were also examined. The results showed that physicochemical properties of biochar were greatly influenced by pyrolysis temperature. Particle size, however, showed little influence on biochar characteristics (p > 0.05). The yield, volatile matter, hydrogen and oxygen contents, and surface functional groups decreased consistently with increasing pyrolysis temperature. An increase in the pH, electrical conductivity, ash, fixed carbon, and specific surface area values was also found. In biochar samples formed at high temperatures (i.e., 550 and 700 °C), Fourier transform infrared spectroscopy-FTIR studies confirmed the increase in aromaticity. Field emission scanning electron microscopy-FESEM images showed differences in the microporous structure and lower size pores at higher temperatures. Biochar pyrolyzed at 700 °C with a particle size of 63–75 µm (i.e., Lv700-63) showed the highest removal efficiency performance. Pb and Cd ions were completely removed (100%) by 0.2 g L−1 Lv700-63 at 7.0 pH and contact times of 120 and 90 min, respectively. The maximum percentage removal of Mn was 86.20% at optimum conditions of 0.2 g L−1 Lv700-63 dosage, 7.0 pH, and 180 min contact time. The findings suggests that the surface complexation, π-electron coordination, and cation exchange were the dominant mechanisms for the Pb, Cd, and Mn removal onto Lv700-63.

Low-molecular-weight aromatic acids mediated the adsorption of Cd2+ onto biochars: effects and mechanisms.

Low-molecular-weight aromatic acids (LWMAAs), a ubiquitous organic substance in natural systems, are important in controlling the environmental fate of potentially toxic metals. However, little is known about the effects of LWMAAs on the interactions between biochars and potentially toxic metals. Herein, the influences of three aromatic acids, including benzoic acid (BA), p-hydroxy benzoic acid (PHBA), and syringic acid (SA), on the adsorption of Cd2+ onto biochars generated at three different pyrolysis temperatures under acidic and neutral conditions were examined. Generally, the adsorption ability of biochars for Cd2+ improved with the increase of pyrolysis temperature, which was ascribed to the increased inorganic element contents (e.g., P, S, and Si) and aromaticity, increasing the complexation between mineral anions and metal ions, and the enhanced cation-π interaction. Interestingly, aromatic acids considerably inhibited the adsorption of Cd2+ onto biochars, which was mainly ascribed to multi-mechanisms, including competition of LWMAA molecules and metal ions for adsorption sites, the pore blocking effect, the weakened interaction between mineral anions and Cd2+ induced by the adsorbed aromatic acids, and the formation of water-soluble metal-aromatic acid complexes. Furthermore, the inhibitory effects of LWMAAs on Cd2+ adsorption intensively depended on the aromatic acid type and followed the order of SA > PHBA > BA. This trend was related to the differences in the physicochemical features (e.g., the octanol/water partition coefficient (log Kow) and molecular size) of diverse LMWAAs. The results of this study demonstrate that the effects of coexisting LMWAAs should not be ignored when biochars are applied in soil remediation and wastewater treatment.