Back to Search Start Over

A novel approach for stabilizing fresh urine by calcium hydroxide addition.

Authors :
Randall DG
Krähenbühl M
Köpping I
Larsen TA
Udert KM
Source :
Water research [Water Res] 2016 May 15; Vol. 95, pp. 361-9. Date of Electronic Publication: 2016 Mar 09.
Publication Year :
2016

Abstract

In this study, we investigated the prevention of enzymatic urea hydrolysis in fresh urine by increasing the pH with calcium hydroxide (Ca(OH)2) powder. The amount of Ca(OH)2 dissolving in fresh urine depends significantly on the composition of the urine. The different urine compositions used in our simulations showed that between 4.3 and 5.8 g Ca(OH)2 dissolved in 1 L of urine at 25 °C. At this temperature, the pH at saturation is 12.5 and is far above the pH of 11, which we identified as the upper limit for enzymatic urea hydrolysis. However, temperature has a strong effect on the saturation pH, with higher values being achieved at lower temperatures. Based on our results, we recommend a dosage of 10 g Ca(OH)2 L(-1) of fresh urine to ensure solid Ca(OH)2 always remains in the urine reactor which ensures sufficiently high pH values. Besides providing sufficient Ca(OH)2, the temperature has to be kept in a certain range to prevent chemical urea hydrolysis. At temperatures below 14 °C, the saturation pH is higher than 13, which favors chemical urea hydrolysis. We chose a precautionary upper temperature of 40 °C because the rate of chemical urea hydrolysis increases at higher temperatures but this should be confirmed with kinetic studies. By considering the boundaries for pH and temperature developed in this study, urine can be stabilized effectively with Ca(OH)2 thereby simplifying later treatment processes or making direct use easier.<br /> (Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
1879-2448
Volume :
95
Database :
MEDLINE
Journal :
Water research
Publication Type :
Academic Journal
Accession number :
27055084
Full Text :
https://doi.org/10.1016/j.watres.2016.03.007