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Phase developments during natural evaporation simulation of Lake Katwe brine based on Pitzer's model
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering, Applied Process Metallurgy. Makerere University, Kampala, Uganda.
KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Energy Processes.ORCID iD: 0000-0001-7995-3151
KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering, Applied Process Metallurgy.
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2014 (English)Conference paper (Refereed)
Place, publisher, year, edition, pages
2014. 254-258 p.
National Category
Chemical Process Engineering
URN: urn:nbn:se:kth:diva-179309OAI: diva2:882502
9th Sida Regional Collaboration Conference, July 20-23, 2014, Entebbe, Uganda
Sida - Swedish International Development Cooperation Agency

QC 20151215

Available from: 2015-12-15 Created: 2015-12-15 Last updated: 2015-12-17Bibliographically approved
In thesis
1. Towards the Improvement of Salt Extraction from Lake Katwe Raw Materials in Uganda
Open this publication in new window or tab >>Towards the Improvement of Salt Extraction from Lake Katwe Raw Materials in Uganda
2015 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Uganda is well endowed with economic quantities of mineral salts present in the interstitial brines and evaporite deposits of Lake Katwe, a closed (endorheic) saline lake located in the western branch of the great East African rift valley. Currently, rudimentally and artisanal methods continue to be used for salt extraction from the lake raw materials. These have proved to be risky and unsustainable to the salt miners and the environment and they have a low productivity and poor product quality. This work involves the investigation of the salt raw materials that naturally occur in the brines and evaporites of Lake Katwe. The purpose is to propose strategies for the extraction of improved salt products for the domestic and commercial industry in Uganda.

The literature concerning the occurrence of salt and the most common available technologies for salt extraction was documented. Also, field investigations were undertaken to characterize the salt lake deposits and to assess the salt processing methods and practices. The mineral salt raw materials (brines and evaporites) were characterized to assess their quality in terms of the physical, chemical, mineralogical, and morphological composition through field and laboratory analyses. An evaluation of the potential of future sustainable salt extraction from the lake deposits was done through field, experimental, and modeling methods. Moreover, the mineral solubilities in the lake brine systems and dissolution kinetics aspects were investigated.

The results reveal that the salt lake raw materials contain substantial amounts of salt, which can be commercialized to enable an optimum production. The brines are highly alkaline and rich in Na+, K+, Cl-, SO42-, CO32-, and HCO3-. Moreover, they contain trace amounts of Mg2+, Ca2+, Br-, and F-. The lake is hydro-chemically of a carbonate type with the brines showing an intermediate transition between Na-Cl and Na-HCO3 water types. Also, the evaporation-crystallization is the main mechanism controlling the lake brine chemistry. These evaporites are composed of halite mixed with other salts such as hanksite, burkeite, trona etc, but with a composition that varies considerably within the same grades. The laboratory isothermal extraction experiments indicate that various types of economic salts such as thenardite, anhydrite, mirabilite, burkeite, hanksite, gypsum, trona, halite, nahcolite, soda ash, and thermonatrite exist in the brine of Lake Katwe. In addition, the salts were found to crystallize in the following the sequence: sulfates, chlorides, and carbonates.

A combination of results from the Pitzer’s ion-interaction model in PHREEQC and experimental data provided a valuable insight into the thermodynamic conditions of the brine and the sequence of salt precipitation during an isothermal evaporation. A good agreement between the theoretical and experimental results of the mineral solubilities in the lake brine systems was observed with an average deviation ranging between 8-28%. The understanding of the mineral solubility and sequence of salt precipitation from the brine helps to control its evolution during concentration. Hence, it will lead to an improved operating design scheme of the current extraction processes. The dissolution rate of the salt raw materials was found to increase with an increased temperature, agitation speed and to decrease with an increased particle size and solid-to-liquid ratio. Moreover, the Avrami model provided the best agreement with the obtained experimental data (R2 = 0.9127-0.9731). In addition, the dissolution process was found to be controlled by a diffusion mechanism, with an activation energy of 33.3 kJ/mol.

Under natural field conditions, the evaporative-crystallization process at Lake Katwe is influenced by in-situ weather conditions. Especially, the depth of the brine layer in the salt pans and the temperature play a significant role on the brine evaporation rates. With the optimal use of solar energy, it was established that the brine evaporation flux can be speeded up in the salt pans, which could increase the production rates. Moreover, recrystallization can be a viable technique to improve the salt product purity. Overall, it is believed that the current work provides useful information on how to exploit the mineral salts from the salt lake resources in the future.


Place, publisher, year, edition, pages
Stockholm: KTH Royal Institute of Technology, 2015. ix, 69 p.
Lake Katwe, salt extraction, brine, evaporites, saltpan, characterization, evaporation - crystallization, solubility, Pitzer ’s ion - interaction model, PHREEQC software, dissolution kinetics, Avrami model.
National Category
Chemical Process Engineering
urn:nbn:se:kth:diva-179445 (URN)
Public defence
2016-01-20, F3, Lindstedtsvägen 26, KTH, Stockholm, 10:00 (English)
Sida - Swedish International Development Cooperation Agency

QC 20151217

Available from: 2015-12-17 Created: 2015-12-16 Last updated: 2015-12-18Bibliographically approved

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