Cd In Biochar Research Articles

Activation of endogenous cadmium from biochar under simulated acid rain enhances the accumulation risk of lettuce (Lactuca sativa L.)

Biochar has been widely applied to remediate heavy metal-contaminated soils, but the environmental risk of the endogenous pollutants in biochar remains unclear. Two biochars with different endogenous cadmium (Cd) concentrations were prepared from background soil (BCB) and contaminated soil (BCC), respectively. We studied the effects of simulated acid rain (SAR) on the activation mechanism of endogenous Cd in biochar and Cd uptake of Cd by lettuce from the biochar-amended soils. SAR aging significantly increased Cd bioavailability by 27.5 % and 53.9 % in BCB and BCC, respectively. The activation of Cd from biochar may be due to the decrease of biochar pH and persistent free radicals (PFRs) and the increase of specific surface area (SSA) and O-contained functional groups in biochars. Two biochars at dosages of 2 % and 5 % rates did not change soil pore water Cd, but BCB and BCC at 10 % increased pore water Cd by 17.3 % and 219 %, respectively after SAR aging. SAR aging significantly increased the bioavailability of Cd in BCB and BCC treated soils than those before SAR aging. BCB application enhanced the biomass of lettuce (Lactuca sativa L.) and decreased the uptake of Cd. However, BCC addition at 10 % decreased the biomass of lettuce and increased the accumulation of Cd. In summary, endogenous Cd in biochar from contaminated soils has a potential environmental risk to plants and human health and the negative effects of endogenous pollutants from the biochars should be further investigated.

Particle size of biochar significantly regulates the chemical speciation, transformation, and ecotoxicity of cadmium in biochar

The pyrolysis of biomass containing excessive heavy metals is likely to produce heavy metal contaminated biochar (BC). Although multiple lines of evidence indicate that higher charring temperature leads to enhanced immobilization of heavy metals in BC, we find that particle size could also play a critical role in the content of heavy metals in BC and BC ecotoxicity. Here, BC derived from cadmium (Cd) enriched rice straw was prepared at different temperatures (300–600 °C) and divided into macro-, colloidal-, and nano-sized fractions, respectively. The content and chemical forms of Cd in BC fractions as well as related algal toxicity were examined. The results show that for the same temperature BC the content of Cd followed an order of colloidal-BC > macro-BC > nano-BC; and the residual fractions of Cd significantly decreased (3.47–16.08%) while that of acid soluble and reducible fractions significantly increased (4.13–16.51% and 0.24–1.71%, respectively) with decreasing particle size of BC. Consistently, colloidal-BC exhibited the highest ecotoxicity for Scenedesmus obliquus. The acid soluble fractions of Cd in macro- and colloidal-BC played a dominating role in their algal toxicity (p < 0.05). However, the ecotoxicity of nano-BC was more dependent on the total content of Cd than specific fractions probably due to the phagocytosis by algal cells. These results indicate that the chemical forms and ecotoxicity of Cd in BC could be remarkably modified by its particle size, which has profound implications for understanding the behavior and potential risk of heavy metal contaminated BC in the environment.

Comparative study on the potential risk of contaminated-rice straw, its derived biochar and phosphorus modified biochar as an amendment and their implication for environment

Direct application of contaminated-rice straw (CRS) to soil can cause the secondary pollution in agricultural land because of high content of Cd in rice straw. This study employed biochar or modified biochar technique to reduce the potential pollution risk of Cd in CRS. In the pot experiment, the CRS, straw biochar prepared at 300 °C (B300) and 500 °C (B500), and phosphorus modified biochar pyrolyzed at 300 °C (PB300) and 500 °C (PB500) were added at dosage of 5% into three typical paddy soils. The results showed that CRS and its derived biochar could enhance soil pH, EC, Eh, organic carbon, exchangeable base cations (K+, Na+, Ca2+ and Mg2+), and available phosphate. The application of CRS, biochar and phosphorus modified biochar significantly increased the contents of total Cd in soils relative to control soil. Compared to CRS, the biochar application (especially the PB500) decreased the contents of 0.01M CaCl2-extractable Cd. The application of CRS significantly increased the content of exchangeable Cd fraction (F1), whereas biochar increased residual Cd content (F4). The biochar and phosphorous modified biochar significantly decreased the contents of bioavailable Cd in soils compared to CRS application. The increased soil pH and dissolve organic matter were found to be the main factors in reducing the release of Cd in biochar. The possible mechanisms of biochar in reducing bioavailability of Cd were to significantly increase soil pH, enhance the complexation of Cd ions, and promote the transformation of Cd from easily available to stable (residual) forms. It could conclude that conversion of contaminated rice straw into biochar was an efficient way to minimize Cd availability in soil and reduce the pollution risk of Cd in rice straw.

Feasibility and risk assessment of heavy metals from low-temperature magnetic pyrolysis of municipal solid waste on a pilot scale

Low-temperature magnetic pyrolysis (LMP) of municipal solid waste (MSW) was conducted in a pilot scale continuous reactor to investigate the distribution and transformation of heavy metals (HMs) in biochar. Environmental safety was evaluated by the risk assessment code (RAC) and the modified potential ecological risk index (MRI). Statistical analyses of HMs revealed that the total concentrations of HMs in biochar was higher than that in MSW and the exchangeable fraction of Cd in biochar under 200 °C and 250 °C were at high risk levels. Temperature increment indicates an increase in regular steps not only migrated more HMs into biochar, but also broke the immobilization of HMs, so resulted in higher environmental risks. The lowest direct toxicity to the environment was obtained by LMP at 200 °C. In light of the residual fraction and the high concentration of HMs in biochar produced in this work, it should be mixed with other uncontaminated plant waste for further application in agriculture. The results of economic assessment reveal that the value of net present value (NPV) and the internal rate of return (IRR) can be positive if high quality bio-products are produced with low operating costs. Optimized design of operation, feedstock and the investment are the key factors to improve the economic feasibility of LMP.

Biochar derived from cadmium-contaminated rice straw at various pyrolysis temperatures: Cadmium immobilization mechanisms and environmental implication

The total concentration, chemical speciation and availability of Cd in biochar derived from Cd-contaminated rice straw were determined to evaluate the potential environmental risk of Cd in biochar and the possibility of biochar as effective way to dispose Cd-contaminated straw. The Cd was concentrated with the increased pyrolysis temperature, while the bioavailability of Cd in biochar was reduced. The sequence extraction indicated that residual fraction of Cd increased and acid exchangeable fraction decreased as pyrolysis temperature increased. The biochar modified by phosphate could significantly reduce the concentration of total and DTPA-extractable Cd in biochar. The pot experiment demonstrated that pyrolysis reduced the potential environmental risk of Cd in biochar. The precipitation and co-precipitation, physical sorption, surface electrostatic interaction, and functional group complexation could be the potential mechanisms of Cd immobilization in biochar. These findings suggested that pyrolysis would be an acceptable and feasible way to dispose contaminated rice straw.

Towards Understanding the Mechanism of Heavy Metals Immobilization in Biochar Derived from Co-pyrolysis of Sawdust and Sewage Sludge.

Biochar was prepared by mixing sewage sludge with sawdust via a co-pyrolysis with different mixture ratios and temperatures. The results showed that the sawdust addition resulted in a lower yield of biochar with higher C content. The total concentrations of Pb and Cd in biochar were reduced. Besides, pyrolysis can transform the potentially toxic Pb and Cd to stable fractions. However the sawdust addition had slight influence on the chemical forms of Pb and Cd in the biochar. The biochar with 50% sawdust at 600°C exhibited a remarkable reduction of the leachable metal concentrations. The possible transformation mechanisms of Pb and Cd were inferred as the formation of aluminum and silicon-containing minerals. These results provide insights into the influence of sawdust addition on the characteristics of biochar and the possible Pb and Cd immobilization mechanisms during co-pyrolysis process.

Pyrolysis of various phytoremediation residues for biochars: Chemical forms and environmental risk of Cd in biochar

Various phytoremediation residues (PMRs), including Brassica napus L. (BN), Pennisetum sinese (PS) and Lolium perenne L.(LP), were pyrolyzed at 400, 500, 600 and 700 °C, respectively. A series of sequential and single extractions were employed to analyze the chemical speciation and potential environmental risk of Cadmium (Cd) in different phytoremediation residues-derived biochars (PMBs). The results showed that the exchangeable Cd fraction decreased but the residual Cd fraction increased, indicating the inhibition of bioavailability of Cd and low potential ecological risk index of PMBs. When the temperature was over 600 °C, the Cd in biochar was acceptable to the environment and the leaching concentration of Cd extracted by the three extraction methods (distilled water, SPLP and TCLP) were all under the standard limit. Findings from this study illustrated that the treatment of pyrolysis was feasible for the three kinds of PMRs at 600 °C with acceptable environment risk.

First “charosphere” view towards the transport and transformation of Cd with addition of manure derived biochar

The specific area between biochar and soil surfaces is termed the “charosphere”, which is analogous to the rhizosphere between plant roots and soil. Physicochemical properties of charosphere soil differ from natural soil. A double-layer mesh bag experiment was conducted to separate the charosphere soil (>2 mm) from biochar (derived from manure pyrolyzed at 300, 500, 700 °C) and the bulk soil. A 95-day experiment determined the availability, total concentration and speciation of Cd in charosphere soil and the total and available Cd in biochar. The availability of Cd decreased in the charosphere soils. Total Cd concentration increased in the biochars but decreased in charosphere soil, suggesting that Cd might transfer from charosphere soil to biochar. Cd in the acid soluble fraction decreased by 25–40% in different biochars while it increased in residue fraction, indicating that Cd tends to be more stable in charosphere soil. Instrumental analysis using SEM, FTIR were performed to provide further evidence of the transport of Cd and to enable interpretation of the mechanisms involved. The phenomena that Cd concentrations change markedly in the charosphere inspires a novel research perspective towards the study of transport and transformation of heavy metals in soil after biochar application.

Stabilization of heavy metals in biochar pyrolyzed from phytoremediated giant reed (Arundo donax) biomass

The pyrolysis of phytoremediated giant reed (Arundo donax) biomass could cause secondary pollution of heavy metals. The stabilization of heavy metals in the pyrolysis process with external materials such as Al2O3, CaCO3, FeCl3 and NaOH, was studied. The results showed that 37% As and 97% Cd in biochar were stabilized when giant reed powder was pyrolyzed at 250 °C with 5% Al2O3 for 2 h. Furthermore, 59% Pb in biochar was stabilized at 400 °C with 5% CaCO3 for 1 h. Under biochar produced in optimized pyrolysis conditions, Cd mainly existed in a residual fraction, while Pb and As mainly existed in oxidizable fraction in BCR analysis. In XRD analysis, As was only found in Ca2As2O7; Cd in biochar mainly existed in Cd (AlCl4)2, CdPbO3 or CdSO3; and Pb mainly existed as Pb3O2SO4.