Optimizing the modification of wood waste biochar via metal oxides to remove and recover phosphate from human urine. Xu Kangning,Zhang Chuke,Dou Xiaomin,Ma Weifang,Wang Chengwen Environmental geochemistry and health The recovery of phosphate from human urine has been considered as one of the most attractive benefits of urine source separation because P is an essential but limited macronutrient. This study investigated the approach to modify wood waste biochar via metal oxides aiming to recover phosphate from human urine to produce a value-added biochar. Results showed the phosphate removal ability was enhanced for the modified biochar pre-treated in modification solutions of MgCl, AlCl, CaCl and FeCl, respectively, while natural biochar released phosphate to urine. Among the tested biochar, Mg-biochar presented the best capacity for phosphate removal from the hydrolyzed urine, reaching 118 mg g at a MgCl concentration of 2.3 M. However, higher MgCl concentration would not further increase the adsorption capacity. Fitting of the adsorption kinetics and isotherms indicated that the phosphate removal process was probably controlled by multiple mechanisms. Both the experimental and fitting results confirmed that the content of Mg oxides was the key factor determining the adsorption rate and capacity of phosphate on Mg-biochar. pH ranges of 7-9 and the ammonium concentration higher than 108 mg L enhanced the phosphate adsorption capacity. As such, the Mg-biochar was more favored for the treatment of hydrolyzed urine rather than fresh urine with acidic pH and lower concentration of ammonium. Further calculations were carried out using the Langmuir model to evaluate the removal of phosphate and the product. Results indicate that it is an effective technique to use Mg-biochar for phosphate removal from hydrolyzed urine and it yields phosphate-enriched biochar products. 10.1007/s10653-017-9986-6

Phosphate and ammonium sorption capacity of biochar and hydrochar from different wastes. Takaya C A,Fletcher L A,Singh S,Anyikude K U,Ross A B Chemosphere The potential for biochar and hydrochar to adsorb phosphate and ammonium is important for understanding the influence of these materials when added to soils, compost or other high nutrient containing environments. The influence of physicochemical properties such as mineral content, surface functionality, pH and cation exchange capacity has been investigated for a range of biochars and hydrochars produced from waste-derived biomass feedstocks. Hydrochars produced from hydrothermal carbonisation at 250 °C have been compared to low and high temperature pyrolysis chars produced at 400-450 °C and 600-650 °C respectively for oak wood, presscake from anaerobic digestate (AD), treated municipal waste and greenhouse waste. In spite of differences in char physicochemical properties and processing conditions, PO4-P and NH4-N sorption capacities ranged from about 0 to 30 mg g(-1) and 105.8-146.4 mg g(-1) respectively. Chars with high surface areas did not possess better ammonium adsorption capacities than low surface area chars, which suggests that surface area is not the most important factor influencing char ammonium adsorption capacity, while char calcium and magnesium contents may influence phosphate adsorption. Desorption experiments only released a small fraction of adsorbed ammonium or phosphate (<5 mg g(-1) and a maximum of 8.5 mg g(-1) respectively). 10.1016/j.chemosphere.2015.11.052

[Effect of Nitrogen on Magnesium Modified Biochar Adsorption to Phosphorus]. Zhi Meng-Meng,Wang Peng-Fei,Hou Ze-Ying,Cao Jing,Chu Zhao-Sheng,Yang Yong-Zhe Huan jing ke xue= Huanjing kexue The effect of ammonia-nitrogen in water on phosphorus removal by magnesium modified biochar (MBC) was developed to increase the utilization of wetland plants. The crystal structures were measured by X-ray powder diffraction (XRD). MBC was prepared using reed as the biomass feedstock, which was modified with magnesium chloride. The raw biochar (BC) was prepared as a control. The removal of phosphate from solution using four different methods, i.e. MBC, BC, BC, and MgCl solutions (BC+Mg) and MgCl solutions (Mg), under different nitrogen to phosphorus molar ratios and initial phosphorus concentrations was investigated in batch experiments. The results demonstrated that the phosphorus removal efficiency of the four treatment methods, which followed the order of MBC>>BC+Mg≈Mg>BC. NH in the solution, promoted phosphorus removal by MBC. In addition, the larger the ratio of nitrogen to phosphorus and the higher the initial phosphorus concentration, the stronger the phosphorus removal capacity of MBC was. In the three treatments with MBC, BC+Mg, and Mg, the XRD analysis showed that NH reacted with Mg and PO in the solution to form MgNHPO·6HO at N:P=5 or 10, promoting the removal of phosphorus. For recycling purposes, waste biomass from constructed wetlands could be used to produce MBC and treat polluted water rich in ammonium and phosphate. Moreover, the ammonium-nitrogen promotes the phosphate removal by MBC. The results from this study provide a new theoretical basis and data support for the treatment of water eutrophication. 10.13227/j.hjkx.201807061

Biochar/struvite composite as a novel potential material for slow release of N and P. Hu Pan,Zhang Yihe,Liu Leipeng,Wang Xinke,Luan Xinglong,Ma Xi,Chu Paul K,Zhou Jichao,Zhao Pengda Environmental science and pollution research international For soil and environmental remediation, biochar/struvite composites are prepared by the crystallization-adsorption method. The recovery rates of N, P, and Mg in the solution increase to 99.02%, 97.23%, and 95.22%, respectively, by forming 10% biochar/struvite composite. X-ray diffraction (XRD) patterns acquired from the 10% biochar/struvite composite show a crystalline structure of MgNHPO·6HO (PDF no. 15-0762) and release of the main nutrient elements (N, P, Mg) from the 10% biochar/struvite composite increases significantly compared to struvite. The solubility of the biochar/struvite composite is the highest in 0.5 mol/L HCl, second in 20 g/L citric acid, and lowest in water. The power function equation describes more precisely the cumulative release of N, P, and Mg from the biochar/struvite composite in distilled water, whereas it follows the simple Elovich equation in 20 g/L critic acid and first-order kinetics equation in 0.5 mol/L HCl. Leaching experiments are performed on the biochar/struvite composite in soil, and the results indicate that the biochar/struvite composite has a longer cycle of release of nutrients than traditional chemical fertilizers and has large potential as a slow-release fertilizer. 10.1007/s11356-019-04458-x

Effects of three kinds of organic acids on phosphorus recovery by magnesium ammonium phosphate (MAP) crystallization from synthetic swine wastewater. Song Yonghui,Dai Yunrong,Hu Qiong,Yu Xiaohua,Qian Feng Chemosphere P recovery from swine wastewater has become a great concern as a result of the high demand for P resources and its potential eutrophication effects on water ecosystems. The method of magnesium ammonium phosphate (MAP) crystallization was used to recover P from simulated swine wastewater, and the effects of three organic acids (citric acid, succinic acid and acetic acid) on P removal efficiency and rate at different pH values were investigated. The results indicated that the P removal efficiency was worst affected by citric acid in the optimal pH range of 9.0-10.5, followed by succinic acid and acetic acid, and the influencing extent of organic acids decreased with the increasing pH value. Due to the complexation between organic acid and Mg(2+)/NH4(+), all of three organic acids could inhibit the P removal rate at the beginning of the reaction, which showed positive correlation between the inhibition effects and the concentration of organic acids. The high concentration of citric acid could completely suppress the MAP crystallization reaction. Moreover, citric acid and succinic acid brought obvious effects on the morphology of the crystallized products. The experimental results also demonstrated that MAP crystals could be obtained in the presence of different kinds and concentrations of organic acids. 10.1016/j.chemosphere.2013.11.019