Pretreatment of lignocellulosic waste as a precursor for synthesis of high porous activated carbon and its application for Pb (II) and Cr (VI) adsorption from aqueous solutions.

Effects of Elm tree sawdust pretreatments using alkali and alkaline earth metals (NaCl, KCl, CaCl2, MgCl2 and Elm tree ash) and deashing solutions (water, HCl, HNO3 and aqua regia) before the carbonization process on the porosity of produced activated carbons and Pb (II) and Cr (VI) adsorption were studied. The activated carbons were characterized by pore size distribution, surface area, FTIR, and SEM-EDX analysies. Based on the results, HCl leaching pretreatment of the biomass increased the activated carbon adsorption capacity of Cr (VI) from 114 to 190 mg g-1. The treatment of biomass with alkali and alkali earth metal salts, especially MgCl2, remarkably increased the activated carbon adsorption capacity of Pb (II) from 233 to 1430 mg g-1. The results indicated that Pb (II) adsorption was attributed to both the mesoporous structure of activated carbon and the abundance of Mg on the activated carbon's surface. On the other hand, the micropores played a major role in Cr (VI) adsorption capacity. The development of the micro- or mesoporous structure of activated carbons through pretreatment of lignocellulosic precursor could be an approach for providing high performance activated carbons for Pb (II) and Cr (VI) removal from aqueous solutions.

Innovative spherical biochar for pharmaceutical removal from water: Insight into adsorption mechanism.

In this study, we developed an innovative spherical biochar with high porosity and excellent paracetamol (PRC) adsorption capacity. The optimal pyrolysis temperatures for the preparation of spherical biochar (derived from pure glucose) and non-spherical biochar (from pomelo peel wastes) were obtained at 900 °C and 700 °C, respectively. Various advanced techniques were applied to characterize the prepared biochars. Spherical and non-spherical biochars exhibited large specific surface area (1292 and 1033 m2/g) and high total pore volume (0.704 and 1.074 cm3/g), respectively. The adsorption behavior of PRC onto two biochars was conducted utilizing batch experiments. Results demonstrated that the adsorption process was slightly affected by the change of solution pH (2-11) and addition of NaCl (0.05-1.0 M) and was able to achieve fast equilibrium (∼120 min). The maximum adsorption capacity of spherical biochar (286 mg/g) for PRC was approximately double that of non-spherical biochar (147 mg/g). The signal of thermodynamic parameters was negative ΔG° and ΔH° values, but positive ΔS° value. The adsorption mechanism consisted of pore-filling, hydrogen bonding formations, n-π and π-π interactions, and van der Waals force. The adsorption capacities of two biochars were insignificantly dependent on different real water samples containing PRC. Consequently, the biochars can serve as a green and promising material for efficiently removing PRC from water.

Synthesis and characterization of magnesium oxide nanoparticle-containing biochar composites for efficient phosphorus removal from aqueous solution.

The effective removal and recovery of phosphorus from aquatic environments are highly important for successful eutrophication control and phosphorus recycling. Herein, we prepared biochar containing MgO nanoparticles (MgO-biochar) by fast pyrolysis of MgCl2-impregnated corn stalks, probed its phosphate adsorption performance. Through the fast pyrolysis, the MgCl2 promoted the formation of micropores and mesoporous, and decomposed into MgO nanoparticles with the size smaller than 100 nm. The adsorption experiments showed that the adsorption property increased with the increase of Mg content, and had a strong correlation with the external surface area. And the phosphate adsorption was well described by the Langmuir-Freundlich model (maximum adsorption capacity was determined as 60.95 mg P/g). Kinetic analysis and characterization analysis of MgO-biochar for different adsorption time indicated that phosphate adsorption onto MgO-biochar was mainly controlled by rapid binding to the external surface (about 75% of the equilibrium adsorption amount), and the uptake rate was limited by the slow diffusion of phosphate into the biochar interior (about 25% of the equilibrium adsorption amount). The results suggested that the synthesized MgO-biochar with enough MgO active site dispersed on a higher external surface can be used as a potential adsorbent for phosphate removal and recovery from aqueous solution.

Preparation of a novel iron-based biochar composite for removal of hexavalent chromium in water.

The chitosan-stabilized ferrous sulfide nanoparticles were loaded on biochar to prepare a composite material FeS-CS-BC for effective removal of hexavalent chromium in water. BC and FeS-CS-BC were characterized by Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) analyses. Batch experiments were employed to evaluate the Cr(VI) removal performance. The experimental results showed that the removal rate of Cr(VI) by FeS-CS-BC(FeS:CS:BC = 2:2:1) reached 98.34%, which was significantly higher than that of BC (44.58%) and FeS (79.91%). In the pH range of 2-10, the removal of Cr(VI) by FeS-CS-BC was almost independent of pH. The limitation of coexisting anions (Cl-、SO42-、NO3-) on Cr(VI) removal was not too obvious. The removal of Cr(VI) by FeS-CS-BC was fitted with the pseudo-second-order dynamics, which was a hybrid chemical-adsorption reaction. The X-ray photoelectron spectroscopy (XPS) analysis result showed that Cr(VI) was reduced, and the reduced Cr(VI) was fixed on the surface of the material in the form of Cr(VI)-Fe(III). Graphical abstract Removal of hexavalent chromium from wastewater by FeS-CS-BC composite synthesized by impregnation.

Magnetic biochar derived from biosolids via hydrothermal carbonization: Enzyme immobilization, immobilized-enzyme kinetics, environmental toxicity.

Magnetic and nonmagnetic biochar (MBC & BC) were produced from biosolids under hydrothermal conditions and characterized in order to understand surface chemistry impacts on enzyme immobilization and activity. Peak surface pore size of MBC was 180 nm and that of BC was 17 nm. Despite similar surface area (≈ 49 m2/g) MBC immobilized more laccase (99 mg/g) than biochar (31 mg/g). For horseradish peroxidase (HRP), the two biochars had similar immobilization capacity (≈ 65 mg/g). Laccase and HRP on MBC had 47.1 and 18.0% higher specific activity than on BC, respectively. The matrix activity of MBC-laccase (33.3 U/mg support) was 3.7-fold higher than BC-laccase (8.8 U/mg support) and higher than the same amount of free laccase (30.2 U) at pH 3.0 (P < 0.05). Although MBC had its own peroxide oxidation activity (104.1 and 165.9 U/mg biochar at pHs 5&6) this only accounted for 16.7 and 20.4% of the total MBC-H RP activity respectively. After 10 wash cycles, MBC still retained 79.3% and 60.3% of laccase and HRP activity, respectively. Additionally, MBC had lower acute toxicity, suggesting that it is relative benign from an environmental perspective.

Synthesis of novel biocomposite powder for simultaneous removal of hazardous ciprofloxacin and methylene blue: Central composite design, kinetic and isotherm studies using Brouers-Sotolongo family models.

Over the past decades, extensive efforts have been made to use biomass-based-materials for wastewater-treatment. The first purpose of this study was to develop and characterize regenerated-reed/reed-charcoal (RR-ChR), an enhanced biosorbent from Tunisian-reed (Phragmites-australis). The second aim was to assess and optimize the RR-ChR use for the removal of binary ciprofloxacin antibiotic (CIP) and methylene blue dye (MB), using Central Composite Design under Response Surface methodology. The third purpose was to explain the mechanisms involved in the biosorption-process. The study revealed that the highest removal-percentages (76.66 % for the CIP and 100 % for the MB) were obtained under optimum conditions: 1.55 g/L of adsorbent, 35 mg/L of CIP, 75 mg/L of MB, a pH of 10.42 and 115.28 min contact time. It showed that the CIP biosorption mechanism was described by Brouers-Sotolongo-fractal model, with regression-coefficient (R2) of 0.9994 and a Person's Chi-square (X2) of 0.01. The Hill kinetic model better described the MB biosorption (R2 = 1 and X2 = 1.0E-4). The isotherm studies showed that the adsorbent surface was heterogeneous and the best nonlinear-fit was obtained with the Jovanovich (R2 = 0.9711), and Brouers-Sotolongo (R2 = 0.9723) models, for the CIP and MB adsorption, respectively. Finally, the RR-ChR lignocellulosic-biocomposite-powder could be adopted as efficient and cost-effective adsorbent.

Preparation of Porous Activated Carbons for High Performance Supercapacitors from Taixi Anthracite by Multi-Stage Activation.

Coal-based porous materials for supercapacitors were successfully prepared using Taixi anthracite (TXA) by multi-stage activation. The characterization and electrochemical tests of activated carbons (ACs) prepared in different stages demonstrated that the AC from the third-stage activation (ACIII) shows good porous structures and excellent electrochemical performances. ACIII exhibited a fine specific capacitance of 199 F g-1 at a current density of 1 A g-1 in the three-electrode system, with 6 mol L-1 KOH as the electrolyte. The specific capacitance of ACIII remained 190 F g-1 even despite increasing the current density to 5 A g-1, indicating a good rate of electrochemical performance. Moreover, its specific capacitance remained at 98.1% of the initial value after 5000 galvanostatic charge-discharge (GCD) cycle tests at a current density of 1 A g-1, suggesting that the ACIII has excellent cycle performance as electrode materials for supercapacitors. This study provides a promising approach for fabricating high performance electrode materials from high-rank coals, which could facilitate efficient and clean utilization of high-rank coals.

A simple novel route for porous carbon production from waste tyre.

In this research, waste tyre rubber was used for activated carbon production with a novel route by modified physo-chemical approach. Potassium hydroxide and carbon dioxide were selected as chemical and physical activating agents, respectively and the process was carried out without carbonization under inert atmospheric conditions. The experiments were designed by applying the central composite design (CCD) as one of the subsets of response surface methodology (RSM). The effects of activation temperature (550-750 °C), activation time (15-75 min), impregnation ratio of KOH/rubber (0.75-3.75) and CO2 flow rate (200-400 mL/min) on production yield and specific surface area of produced activated carbon were studied. Based on the results, the 2FI and quadratic models were selected for production yield and specific surface area, respectively. The activation temperature was the main effective parameter on both responses in this process. The production yield and specific surface area of produced activated carbon at optimized conditions for each model were 47% and 928 m2/g, respectively. BET, XRF, XRD, FT-IR, EDS and FE-SEM analyses were carried out on the optimized sample of specific surface area model in order to investigate the residual salts and morphological porous structures. Based on the surface properties and the presence of sulfur compounds in produced activated carbon, this activated carbon has the ability of eliminating heavy metals such as mercury from industrial waste water.

Bone-derived biochar and magnetic biochar for effective removal of fluoride in groundwater: Effects of synthesis method and coexisting chromium.

The presence of fluoride in groundwater in excess of 1.5 mg L-1 is a major environmental health concern, and biochar is a promising low-cost adsorbent for the treatment of such water. In the present study, pristine and magnetic biochars were synthesized by peanut hull and bovine bone for the adsorption of fluoride. The biochars were systematically characterized by SEM-EDS, BET, XRD, VSM, FT-IR, and XPS. The experiment results showed that the magnetic biochar prepared by soaking biomass in FeCl3 solution and then pyrolyzing ("prepyrolysis") had a higher adsorption capacity than that prepared by mixing pristine biochar with Fe2+ /Fe3+ solution and then treating with NaOH ("postpyrolysis"). The bone-derived biochar and magnetic biochar exhibited high adsorption capacity of fluoride (>5 mg g-1 ) due to the presence of hydroxyapatite (HAP) and γ-Fe2 O3 . The 0.1 M NaOH solution could be optimal desorption agent, and the adsorption-desorption experiments indicated the bone biochars maintained the reasonable adsorption capacity after several cycles. Moreover, the coexisting Cr(VI) and fluoride could be removed simultaneously by bone-derived biochars. It is suggested that bovine bone-derived pristine and magnetic biochars can be used as preferential adsorbents for fluoride removal from contaminated groundwater. PRACTITIONER POINTS: Bone-derived pristine and magnetic biochars exhibit high adsorption capacity for fluoride in weakly alkaline solution. The presence of hydroxyapatite and γ-Fe2 O3 in bone-derived biochars plays an important role for fluoride adsorption. Magnetic biochars prepared by soaking biomass in FeCl3 solution and then pyrolyzing ("prepyrolysis") perform better. The coexisting Cr(VI) and fluoride can be simultaneously removed in groundwater by bone biochars.

Effects of pyrolysis temperature and addition proportions of corncob on the distribution of products and potential energy recovery during the preparation of sludge activated carbon.

The potential energy recovery during sludge activated carbon (SAC) preparation by co-pyrolysis of sewage sludge and biomass has recently gained significant attention. This study firstly evaluated the distribution of pyrolysis products including SAC, oils and gases during sludge pyrolysis at different temperatures (400 °C-800 °C) and corncob addition proportions (0-50%, w/w). The results demonstrated that with the increase of pyrolysis temperature, yield of SAC declined dramatically, while yields of pyrolysis oils and gases increased. With increasing addition of corncob, the yields of SAC and pyrolysis oils declined slightly, while the yield of gases generally increased. Then, the potential energy recovery during sludge pyrolysis was calculated, and the highest energy recovery value was 10.21 kJ/g achieved at 800 °C and 50% corncob addition. However, higher pyrolysis temperature over 600 °C resulted in lower yield and iodine adsorption capacity of SAC. Therefore, the suitable conditions were suggested to be at 600 °C with 50% corncob addition considering both adsorption performance of SAC and potential energy recovery efficiency.

Evaluation of activated carbon synthesized by one-stage and two-stage co-pyrolysis from sludge and coconut shell.

Waste biomass and sewage sludge were used to obtain an adsorbent material with excellent performance qualities by adopting a KOH activation process via one-stage (ACone) or two-stage (ACtwo) co-pyrolysis. The main purpose of this work was to investigate the effects of both methods in terms of the physicochemical properties and adsorption capacities for methylene blue (MB). Textural analyses revealed that the surface area (Stot= 683.82 m2/g) and total pore volume (Vtot= 0.72 cm3/g) of ACtwo were more than two-fold compared with ACone (Stot= 285.33 m2/g; Vtot= 0.35 cm3/g). Thus, two-stage co-pyrolysis produced activated carbon with increased porosity, which was favorable for MB adsorption. Nevertheless, the intensity of the surface functional groups of ACtwo was weaker than for ACone, which could be due to the pore-forming mechanism. Two-stage co-pyrolysis increased the yield and aromaticity of activated carbon, but sufficient activation caused more functional groups to decompose. For the adsorbate MB, the maximum adsorption capacity of ACtwo (602.80 mg/g) was more than five-fold greater than that of ACone (101.88 mg/g), due to its excellent porosity properties. Furthermore, the interactions of MB molecules with activated carbon were via hydrogen bonds and electrostatic attraction. The adsorption process of MB onto activated carbon was accurately described by the pseudo-second-order kinetic model. Adsorption equilibrium evaluated Langmuir isotherms demonstrated that MB formed a monolayer by adsorption onto the activated carbon. Adsorption thermodynamics was used to investigate the influence of temperature on the adsorption process. Thermodynamic parameters indicated that MB adsorption onto activated carbon was spontaneous and endothermic. In conclusion, our results showed that two-stage co-pyrolysis improves the adsorption capabilities of activated carbon, so achieving better economic value from waste materials.

Synthesis of biochar from chili seeds and its application to remove ibuprofen from water. Equilibrium and 3D modeling.

In this work chili seeds (Capsicum annuum) were used as raw material in the synthesis of biochar at temperatures between 400 and 600 °C. The samples were chemically, texturally and morphologically characterized and their properties were correlated with the calcination temperature. The adsorption mechanism of IBP was elucidated by analyzing the effect of solution pH, ionic strength and temperature, whereas that, the intraparticle diffusion mechanism was clarified through the application of a 3D diffusional model. The results evidenced that raising the pyrolysis temperature promotes a greater content of disordered graphitic carbon (51.6-85.02%) with small surface area (0.52-0.18 m2/g) and low quantity of functional groups. The adsorption study demonstrated that the biochar synthesized at 600 °C (C600) enhances the adsorption capacity >50 folds compared with chili seeds. Moreover, at pH = 7 the adsorption mechanism is governed by π-acceptor and attractive electrostatic interactions, whereas at basic pH the main adsorption mechanism is π-acceptor. Additionally, hydrophobic interactions become important by increasing the presence of NaCl. The application of 3D diffusional model based on surface diffusion interpreted clearly the kinetic curves obtaining values of Ds ranging from 2.31 × 10-8-2.51 × 10-8 cm2 s-1. Besides, it was determined that intraparticle mass flux is larger along the shortest axis of the seed, and always directed toward the particle center. The maximum mass flux takes place in the center of particle, and it advances like a moving front as time was increased.

Effective Removal of Congo Red by Triarrhena Biochar Loading with TiO2 Nanoparticles.

A composite of pyrolytic Triarrhena biochar loading with TiO2 nanoparticles has been synthesized by the sol-gel method. The composite shows a well-developed hollow mesoporous and macropore structure as characterized by XRD, BET, and SEM. When used as an absorbent to remove Congo red from aqueous solution, it was found that as-prepared composite performed better absorption capacity than single biochar or TiO2. The results suggest that biochar loading with TiO2 could be promisingly implemented as an environmentally friendly and inexpensive adsorbent for Congo red removal from wastewater.

Synthesis of a stable magnesium-impregnated biochar and its reduction of phosphorus leaching from soil.

Biochar improves soil fertility and promotes long-term terrestrial carbon sequestration. However, biochar seems not to be stable enough due to physical, chemical and biological reactions. In this study, a novel, stable, and magnesium (Mg)-impregnated biochar was prepared from cow dung and applied to decrease P leaching from soil. XPS, FTIR, XRD, SEM and EDS were used to evaluate the effect of modification and phosphorus(P) sorption on the oxidation resistance of biochar. The results showed that the oxidation resistance of the Mg-impregnated biochar was improved by the formation of MgO on its surface. The soil column experiment indicated that the Mg-impregnated -biochar decreased P loss from leaching by 89.25%. In addition, the available P content of the soil surface layer under Mg-impregnated biochar treatment increased by 3.5-fold relative to that under the control treatment. P sorption also enhanced the oxidation resistance of biochar. The relative contents of CO, CO, and COOH on the surface of P-laden biochar was 20.97% and was lower than those on the surface of biochar without P sorption (33.15%). Oxidation resistance was enhanced by the formation of new MgP crystals, which prevented the oxidation of CC, CC, and CH into CO, CO, and COOH, respectively, by acting as a physical barrier between the biochar surface and oxygen. The results of XRD, SEM and EDS provided evidence for the formation of MgP crystals. Overall, results indicated that the Mg-impregnated biochar can reduce P leaching loss from soil and has enhanced stability.

Biochar-based functional materials in the purification of agricultural wastewater: Fabrication, application and future research needs.

Nowadays, agricultural contamination is becoming more and more serious due to the rapid growth of agricultural industry, which discharged antibiotics, pesticides or toxic metals into farmlands. A large number of researchers have applied biochar-based functional materials to the treatment of agricultural wastewater contamination. Meanwhile, biochar has also proved to be a very promising and effective technology in water purification field due to its various beneficial properties (e.g., cost effective, high specific surface area, and surface reactive groups). The focus of this review is to highlight the fabrication methods and application of biochar-based functional materials with the removal of different agricultural contaminants, and discuss the underlying mechanisms. However, the application of biochar-based functional materials is currently under its infancy, with the main hindrance is identified as the gap between laboratory scale and field application, immaturity of engineered biochar production technologies, and lack of quality standards. In order to fill these knowledge gaps, more efforts should be made to pay for the relevant research in future studies.

Phosphorus recovery and reuse by pyrolysis: Applications for agriculture and environment.

Phosphorus ore extraction for soil fertilization supports the demand of modern agriculture, but extractable resource limitations, due to scarcity, impose a P reuse and recycling research agenda. Here we propose to integrate biochar production (pyrogenic carbon) with municipal and agricultural waste management systems, to recover and reuse phosphorous that would otherwise be lost from the ecological food web. A meta-analysis and available data on total P in biochar indicated that P-enriched feedstocks include animal manure, human excreta, and plant-biomass collected from P-polluted sites. Phosphorus in biochar could participate in P equilibriums in soils and is expected to supply P. The release, sorption and desorption of P by biochar will codetermine the potential of P replenishment by biochar and P loss from biochar-amended soils. Abiotic and biotic factors are expected to affect sorption/desorption of P between biochar and soil aggregates, and P acquisition by plants. Chemical extraction, using acid or alkaline solutions, is considered as a means for P retrieval from high P biochar, especially for biochar with high heavy metal contents. To bridge the gap between academia and practice, this paper proposes future development for phosphorus acclamation by pyrolysis: 1) identification of high-P bio-waste for pyrolysis; 2) retrieval of P by using biochar as soil amendment or by chemical leaching; 3) biochar modification by inorganic nutrients, P solubilizing microorganisms and other organic matter; and 4) compatible pyrolysis equipment fit to the current waste management context, such as households, and waste water treatment plants.

Synthesis and characterization of a novel magnetic biochar from sewage sludge and its effectiveness in the removal of methyl orange from aqueous solution.

A novel magnetic biochar from sewage sludge (MSBC) using SrFe12O19 as magnetic substrate was successfully synthesized under high-temperature and oxygen-free conditions. Several techniques and methodologies (X-ray diffraction, Fourier transform infrared spectroscopy and vibrating sample magnetometer) were used to determine the surface functional groups and physicochemical properties of MSBC, which showed that the MSBC combined the features of both SrFe12O19 and sludge biochar (SBC). And then the adsorption behavior of methyl orange (MO) from aqueous solution onto the MSBC was investigated. And the influence of variables including pH, initial concentration of MO, adsorbent dosage and contact time was studied in detail. The optimal adsorption amount of MO (149.18 mg·g-1) was obtained with 600 MO mg·L-1, 2 MSBC g·L-1, at pH of 5 for 40 min. The equilibrium data were evaluated using Langmuir and Freundlich isotherms. The Langmuir model better described the absorption of MO. Besides, the kinetic data were analyzed using pseudo-first-order and pseudo-second-order equations, and the pseudo-second order exhibited the better fit for the kinetic studies (R2 = 0.9982). This study showed that MSBC could be utilized as an efficient, magnetically separable adsorbent for the environmental cleanup.

Biochar provides a safe and value-added solution for hyperaccumulating plant disposal: A case study of Phytolacca acinosa Roxb. (Phytolaccaceae).

In this work, an innovative approach using biochar technology for hyperaccumulator disposal was developed and evaluated. The heavy metal enriched P. acinosa biomass (PBM) was pyrolyzed to produce biochar (PBC). Both PBM and PBC were characterized with X-ray diffraction (XRD) for crystal phases, scanning electron microscopy (SEM) for surface topography, and analyzed for elemental composition and mobility. The results revealed that whewellite, a dominant crystal form in biomass, was decomposed to calcite after pyrolysis. Elemental analysis indicated that 91-99% total non-volatile elements in the biomass were retained in the biochar. The toxicity characteristic leaching procedure (TCLP) results revealed that 94.6% and 0.15% of total Mn was extracted for biomass and biochar, respectively. This suggests that mobility and bioavailability of Mn in biochar was much lower relative to pristine biomass. Batch sorption experiment showed that excellent removal of aqueous silver, lead, cadmium, and copper ions can be achieved with PBC. Findings from this work indicated that biochar technology can provide a value-added solution for hyperaccumulator disposal.

Study of ciprofloxacin adsorption and regeneration of activated carbon prepared from Enteromorpha prolifera impregnated with H3PO4 and sodium benzenesulfonate.

Activated carbons were derived from Enteromorpha prolifera immersed in H3PO4 solution or the H3PO4 solution mixed with sodium benzenesulfonate (SBS), producing AC and AC-SBS. NaOH solution was employed in regeneration of ciprofloxacin (CIP)-loaded AC and AC-SBS to obtain RAC and RAC-SBS. The properties of the original and regenerated activated carbons were characterized by thermo-gravimetric analysis (TGA), scanning electron microscopy (SEM), N2 adsorption/desorption isotherms and Fourier transform infrared spectroscopy (FTIR). Batched adsorption studies were carried out to compare CIP adsorption behaviors of the four carbons. The results suggested that the four samples exhibited higher proportions of mesopores and similar functional groups. Although AC displayed much higher specific surface area (SBET) (1045.79m2/g) than AC-SBS (738.03m2/g), its CIP adsorption capacity was much less than AC-SBS. The maximum adsorption capacity for AC, AC-SBS, RAC and RAC-SBS were found to be 250mg/g, 286mg/g, 233mg/g and 256mg/g, respectively, with the isotherms adhering to Langmuir isotherm model. The electrostatic attraction and cation exchange between CIP and the four carbons were the dominant adsorption mechanisms. Moreover, the thermodynamic parameters represented that the adsorption process had been confirmed to be a spontaneous and endothermic reaction.

Cumulative effects of bamboo sawdust addition on pyrolysis of sewage sludge: Biochar properties and environmental risk from metals.

A novel type of biochar was produced by mixing bamboo sawdust with sewage sludge (1:1, w/w) via a co-pyrolysis process at 400-600°C. Changes in physico-chemical properties and the intrinsic speciation of metals were investigated before and after pyrolysis. Co-pyrolysis resulted in a lower biochar yield but a higher C content in the end product compared with use of sludge alone as the raw material. FT-IR analysis indicates that phosphine derivatives containing PH bonds were formed in the co-pyrolyzed biochars. In addition, co-pyrolysis of sludge with bamboo sawdust transformed the potentially toxic metals in the sludge into more stable fractions, leading to a considerable decrease in their direct toxicity and bioavailability in the co-pyrolyzed biochar. In conclusion, the co-pyrolysis technology provides a feasible method for the safe disposal of metal-contaminated sewage sludge in an attempt to minimize the environmental risk from potentially toxic metals after land application.