Synthesis of porous iron hydroxy phosphate from phosphate residue and its application as a Fenton-like catalyst for dye degradation

Phosphate residue is a kind of hazardous solid waste and if not properly disposed of, could cause serious environmental contaminations. The abundant iron salt available in phosphate residue can be used to prepare photo-Fenton catalytic reagent for wastewater treatment. In this study, the phosphate residue was effectively purified by a hydrothermal recrystallization method, reaching an iron phosphate purity of 94.2%. The particles of iron phosphate were further processed with ball milling with their average size reduced from 19.4 to 1.6 μm. By hydrothermal crystallization of iron phosphate and thermal decomposition of oxalate precursor, porous iron hydroxy phosphate was prepared. The modified porous iron hydroxy phosphate(m-PIHP) of higher surface area with iron oxalate on its surface can degrade 98.87% of Rhodamine B in 15 min. Cyclic experiment showed that the catalyst still had a good catalytic activity after six cycles( > 40%). The X-ray photoelectron spectroscopy results showed that the iron oxalate complex on the catalyst surface decomposed to produce ferrous ions and accelerated the rate of · OH production. The current work demonstrated that the m-PIHP synthesized from phosphate residue and modified with iron oxalate can be used as an effective dye wastewater treatment agent.

Thermogravimetric coupled with Fourier transform infrared analysis study on thermal treatment of monopotassium phosphate residue

In China,safe disposal of hazardous waste is more and more a necessity,urged by rapid economic development.The pyrolysis and combustion characteristics of a residue from producing monopotassium phosphate(monopotassium phosphate residue),considered as a hazardous waste,were studied using a thermogravimetric,coupled with Fourier transform infrared analyzer(TGFTIR).Both pyrolysis and combustion runs can be subdivided into three stages:drying,thermal decomposition,and final devolatilization.The average weight loss rate during fast thermal decomposition stage in pyrolysis is higher than combustion.Acetic acid,methane,pentane,(acetyl)cyclopropane,2,4,6-trichlorophenol,CO,and CO_(2) were distinguished in the pyrolysis process,while CO_(2) was the dominant combustion product.

Phosphate adsorption performance of a novel filter substrate made from drinking water treatment residuals

Phosphate is one of the most predominant pollutants in natural waters. Laboratory experiments were conducted to investigate the phosphate adsorption performance of a（NFS） made from drinking water treatment residuals. The adsorption of phosphate on the NFS fitted well with the Freundlich isotherm and pseudo second-order kinetic models. At p H 7.0, the maximum adsorption capacity of 1.03 mg/g was achieved at 15°C corresponding to the wastewater temperature in cold months, and increased notably to 1.31 mg/g at 35°C.Under both acidic conditions（part of the adsorption sites was consumed） and basic conditions（negative charges formed on the surface of NFS, which led to a static repulsion of PO43-and HPO42-）, the adsorption of phosphate was slightly inhibited. Further study showed that part of the adsorption sites could be recovered by 0.25 mol/L Na OH. The activation energy was calculated to be above 8.0 k J/mol, indicating that the adsorption of phosphate on NFS was probably a chemical process. Considering the strong phosphate adsorption capacity and recoverability, NFS showed great promise on enhancing phosphate removal from the secondary treated wastewater in the filtration process.