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Article
Publication date: 1 December 2005

Zbigniew Wzorek, Katarzyna Gorazda, Dorota Minda and Joanna Kulczycka

This paper sets out to observe the changes occurring during thermal processing of Na2CO3 and FePO4 · 2H2O in control trials, then analyses the influence on availability of…

Abstract

Purpose

This paper sets out to observe the changes occurring during thermal processing of Na2CO3 and FePO4 · 2H2O in control trials, then analyses the influence on availability of phosphorus compounds in comparison with pure FePO4 · 2H2O.

Design/methodology/approach

Control trials of Na2CO3/FePO4 · 2H2O with molar ratios in the range 0.5‐5.0 were heated to a temperature of 850°C, then calcined within 3 hours without mixing. Cooled products were submitted for chemical analysis regarding the content of phosphorus soluble in cold water, 0.4 percent HCl, 2 percent citric acid and aqua regia as well as crystallographic identification.

Findings

The addition of Na2CO3 significantly increases the availability of phosphorus compounds from FePO4 · 2H2O. The total amount of phosphorus in control trials after the calcining process is soluble in cold water, citric acid and HCl. The molar ratios used affect the type of crystalline phase formation only in the case of a molar ratio near to 1.0. Near‐perfect phosphorus availability in hematite phase formation was observed.

Practical implications

These preliminary results confirm the necessity for further investigation of the addition of Na2CO3 into industrial sewage sludge before the calcining process. The results may allow for a decrease in energy use during the combustion process and may create the possibility of recovering phosphorus compounds from ash using only cold water instead of mineral acids during the extraction process.

Originality/value

This paper is a new source of information about phosphorus recovery from sewage sludge.

Details

Management of Environmental Quality: An International Journal, vol. 16 no. 6
Type: Research Article
ISSN: 1477-7835

Keywords

Article
Publication date: 1 December 2005

Zbigniew Wzorek, Katarzyna Gorazda, Joanna Kulczycka and Tadeusz Rzepecki

To determine the influence of alkali components (especially Ca compounds) on the hematite phase formation during thermal processing of sewage sludge and the observation of…

Abstract

Purpose

To determine the influence of alkali components (especially Ca compounds) on the hematite phase formation during thermal processing of sewage sludge and the observation of transformations proceeding at different ratios of Ca to FePO4.

Design/methodology/approach

The model compositions were heated to temperatures of 600°C and 950°C, then calcined within 3 hours without mixing. Cooled products were subjected chemical analysis regarding the content of phosphorus that was soluble in cold water, 0.4 per cent HCl, 2 percent citric acid and aqua regia as well as crystallographic identification.

Findings

On calcining at 600°C, CaO reacts with FePO4, forming hydroxylapatite. The hematite phase which is insoluble in mineral acids crystallizes above 600°C. Further increasing the calcining temperature leads to transformations resulting in Ca9Fe(PO4)7 and hematite formation. Molar ratios of CaO to FePO4 · 2H2O of 1.0 and 2.0 lead to hematite phase formation and increase the availability of phosphorus compounds (characterized by phosphate solubility in 0.4 percent HCl and 2 percent citric acid) in compositions after calcining.

Practical implications

The addition of CaO to sewage sludge before the combustion process should be beneficial from the point of view of further extraction of phosphorus compounds from the ash obtained. Suitable CaO addition favours iron binding into the hematite phase and raises the solubility of the phosphorus compounds in the ashes formed.

Originality/value

This paper is a new source of information which complements existing knowledge about phosphorus recovery from sewage sludge.

Details

Management of Environmental Quality: An International Journal, vol. 16 no. 6
Type: Research Article
ISSN: 1477-7835

Keywords

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