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Nitrogen conversion (N-conversion) mechanism of spirulina (SP) in hydrothermal carbonization (HTC) was investigated under medium-low temperature (180-280 °C). N-conversion in bio-char, liquid and bio-oil were studied by FTIR, XPS, GC-MS and other analytical methods. Results indicated that the temperature could significantly affect the evolution of nitrogen. At 180-200 °C, the content of protein-N and pyridine-N in bio-char fell 23.01% and 9.51% respectively. In contrast, the contents of inorganic-N and quaternary-N increased by 16.99% and 16% respectively. Protein-N hydrolysis and Maillard reaction produced the key intermediate compounds, including amines, amides and N-heterocyclic compounds during the HTC. At 200-280 °C, the inorganic-N was obviously converted from solid to liquid. With the increased of temperature, it would enhance the polymerization of pyrrole-N and pyridine-N, which could cause the significant increase of aromatic N-heterocyclic compounds (e.g., nitriles and indole derivatives) in bio-oil. A N-conversion mechanism of SP HTC was proposed in this study., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

This study explored the cooperative effects of hydrothermal or activators pretreatment and pyrolysis process on the chemical composition of bean dreg (BD)-derived carbon materials and its adsorption characteristics for methylene blue (MB) further. The results showed that hydrothermal assisted pyrolysis carbon with or without activator (HBK and HB) possess higher BET surface area than no hydrothermal assisted carbon (BKs and B, respectively). But surface area alone was not a critical factor contributing to MB adsorption, it also depends on strong electrostatic interaction and the hydrogen bonding interaction between N + in MB combines with OH and COO - group of adsorbent surface by pH-dependent adsorption and pseudo-second-order model. Additionally, BK800 (pyrolysis at 800 °C) was identified as the most efficient adsorbent due to maximum adsorption capacity (434.78 mg g -1 ), and BDP (BD-derived polymer composite hydrogel), possessing excellent adsorption property and high reusability, made BK800 easier to separate from the regenerated dye solution., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Co-hydrothermal carbonization of food waste-woody biomass blend was conducted to enhance the pelletization and hydrochar-fuel properties. The hydrochar was characterized by proximate, elemental analysis and HHVs, whilst energy consumption of pelletization, tensile strength, and combustion characteristics of hydrochar pellets were evaluated. Results showed that food waste (FW) blended with 0-50% mainly decreased H/C of hydrochar, while blend ratio from 75% to 100% mainly decreased O/C. When FW blended from 0% to 75%, the energy consumption for hydrochar palletization decreased about 12-17 J, whereas tensile strength of pellets increased about 2.4-5.5 MPa by formation of solid bridge when woody biomass (WS) ratio was increased. The hydrochar pellets from high ratio FW had decreased ignition temperature and maximum weight loss rate with wider temperature range, indicating the increased flammability and moderate combustion. These findings demonstrate that HTC of food waste-woody biomass blend was suitable for pelletization towards solid biofuel production., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

This study investigated the clean properties and combustion behavior of hydrochar from food waste (FW). The hydrochar was characterized by proximate analysis and HHVs, and the chemical forms were investigated by FTIR, XPS (Sulfur), and XANES (Chlorine). TG-FTIR was used to assess the combustion behaviors, and XRF was used to assess the fouling and slagging inclinations. Results showed that increasing temperature from 180 °C to 260 °C enhanced the removal of N, S, and Cl for hydrochar. Especially, aromatic-S and sulfate-S increased in contrast to sulfoxide-S, and more inorganic-S was produced in hydrochar; all samples had mainly inorganic-chlorine. Additionally, the release of HCl, SO 2 , and NO of hydrochar combustion were significantly reduced and the SI and FI index decreased to ranges of 0.18-0.16 and 0.32-0.17, respectively. However, hydrochar produced at temperature above 220 °C led increased NO emission possibly due to formation of more pyridine-N and quaternary-N., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

The influence of temperature (180-260°C) on the fate of nitrogen during hydrothermal carbonization (HTC) of food waste (FW) was assessed. The distribution and evolution of nitrogen in aqueous products and bio-oil, as well as hydrochar, were conducted. Results suggested that elevated temperature enhanced the deamination and the highest ammonium concentration (929.75mg/L) was acquired at 260°C. At temperatures above 220°C, the total N in the hydrochar became stable, whereas the mass percentage of N increased. Amines and heterocyclic-N compounds from protein cracking and Maillard reactions were identified as the main nitrogen-containing compounds in the bio-oil. As to the hydrochar, increasing temperature resulted in condensed nitrogen-containing aromatic heterocycles (e.g. pyridine-N and quaternary-N). In particular, remarkable Maillard reactions at 180°C and the highest temperature at 260°C enhanced nitrogen incorporation (i.e. quaternary-N) into hydrochar., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

In this study, the effect of feedwater pH (3-11) on phosphorus (P) transformation during the hydrothermal carbonization (HTC) of sewage sludge (SS) was investigated at a temperature range of 200-260°C. The HTC significantly accumulated P in the hydrochar. Different feedwater pH stimulated the transformation of various forms of P. An acidic feedwater pH promoted the transformation of apatite phosphorus (AP) to non-apatite inorganic phosphorus (NAIP), and of organic P (OP) to inorganic P (IP). The NAIP tended to transformation to AP and a small part of the IP was transformed to OP when the SS was treated in a basic environment. The combination of three P analysis methods (chemical extractive fractionation, X-ray powder diffraction (XRD) and energy dispersive spectroscopy (EDS)) showed that metal cations (e.g. Al and Ca) and the pH played important roles in the transformation of different forms of P during the HTC of the SS., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

In this study, the effect of feed-water pH (pH=2-12) on fate and risk of heavy metals (HMs) in hydrochars (HCs) was investigated. Hydrothermal carbonization (HTC) of sewage sludge (SS) was carried out with different feed-water pH at 270°C. The research results showed that changing feed-water pH had a positive effect on accumulating Pb, Ni, Cd and Zn in HCs. Chemical forms of Cu and Cr converted from an unstable state to stable in the alkaline environment while in the acidic condition was opposite. The effect of feed-water pH on the chemical forms of HMs was variable but not significant. Risk assessments of Igeo, Er(i), RAC and RI were applied to evaluate the accumulation levels of individual metal, the potential ecological risks, the bio-availabilities and the comprehensive toxicity and sensitivity of HMs, respectively. The lowest pollution level of HMs was obtained at 270°C with pH=11., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

The fate and risk assessment of heavy metals (HMs) in solid residue from co-liquefaction of sewage sludge (SS) and Camellia oleifera cake (COC) in supercritical ethanol (SCE) were investigated. SCE effectively stabilized HMs in solid residues and a better stabilization was presented on Zn than Cd. Moreover, SCE significantly transformed Cd, Cu and Zn into F4, which reduced the risk to the environment. Furthermore, risk assessments of Igeo, Er(i), RI and RAC demonstrated that the addition of COC was beneficial to the contamination decrement of HMs since pollution levels of HMs all decreased after treatment, and the lowest pollution level was obtained with SC-350. Therefore, SS treated by SCE with the addition of COC could be a promising technology for disposal of SS, especially considering the safety of COC as regards HMs problem., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

The influence of sewage sludge-based activated carbons (SSAC) on sewage sludge liquefaction has been carried out at 350 and 400°C. SSAC increased the yield and energy density of bio-oil at 350°C. The metallic compounds were the catalytic factor of SSAC obtained at 550°C (SSAC-550), while carbon was the catalytic factor of SSAC obtained at 650°C. Liquefaction with SSAC redistributed the species of heavy metals in solid residue (SR). With the addition of SSAC, the risk of Cu, Zn and Pb decreased at 350°C, while at 400°C the risk of Cd, Cu, and Zn were decreased. Ecological risk index indicated that 400°C was preferable for the toxicity decrement of SR, while risk assessment code indicated that SR obtained at 350°C contained lower risk. Considering the bio-oil yield, liquefaction at 350°C with SSAC-550 was preferable., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

The aim of this work is to evaluate the adsorption performances of activated carbon derived from sewage sludge (ACSS) for gaseous formaldehyde removal compared with three commercial activated carbons (CACs) using self-designing adsorption and distillation system. Formaldehyde desorption of the activated carbons for regeneration was also studied using thermogravimetric (TG) analysis. The porous structure and surface characteristics were studied using N2 adsorption and desorption isotherms, scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The results show that ACSS has excellent adsorption performance, which is overall superior to the CACs. Adsorption theory indicates that the ACSS outperforms the CACs due to its appropriate porous structure and surface chemistry characteristics for formaldehyde adsorption. The TG analysis of desorption shows that the optimum temperature to regenerate ACSS is 75°C, which is affordable and economical for recycling., (Copyright © 2010 Elsevier Ltd. All rights reserved.)