geothermal brine
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2021 ◽  
Author(s):  
◽  
Mauro Passarella

<p><b>To investigate the interaction between fluids and basalt at subcritical, near-supercritical, and supercritical hydrothermal conditions (350-400˚C/500 bar), eight experiments have been conducted. These used a continuous-flow, high temperature and pressure hydrothermal apparatus. The basalt was reacted with three fluids: distilled water; geothermal brine; and natural seawater. Two further experiments used only seawater as a control to determine its behaviour without the influence of basalt.</b></p> <p> With distilled water, the fluid chemistry results show elevated SiO2, K, Cl, SO4, and H2S in solution for the first 12 days of both experiments. This is due to volcanic glass dissolution. After glass was removed, fluid composition was controlled by the remaining rock minerals. At 400˚C, the secondary mineral assemblage at the bottom of the Reactor (fluid entry point) is composed of grossular, wollastonite, anorthite, and chlorite. These results show the effectiveness of distilled water, which lacks any alkali cations, at removing Na and K rapidly from the rock. At the top of the Reactor (fluid exit point) the secondary minerals are anorthite and celadonite. At 350˚C, the secondary mineral assemblage at the bottom is anorthite and chlorite, while celadonite is the dominant secondary mineral at the top. In both experiments, celadonite replaces solely olivine. The formation of celadonite through reaction with distilled water shows that it can be formed by the interaction of deuteric water and basalt without addition of other components.</p> <p> The geothermal brine contains high concentrations of SiO2, K, SO4, Na, Cl and has an acidic pH. At 400˚C, fluid chemistry displays elevated SiO2 concentrations for approximately two weeks due to glass dissolution. At 350˚C, SiO2 concentration is initially high after temperature increase, but decreases gradually over the remainder of the experiment. At 400˚C, the secondary mineral assemblage at the bottom of the Reactor is composed of anhydrite and biotite, while at the top of the Reactor, smectite is the only secondary mineral. At 350˚C, anhydrite and smectite are found at the bottom, while only smectite is found at the top. The lack of biotite at 350˚C suggests this mineral’s precipitation kinetics are too slow to outcompete chlorite precipitation.</p> <p> The seawater-only experiments were conducted as controls to determine its behaviour during heat-up and provide the input solution composition for the seawater-basalt experiments. Both seawater-only experiments (377˚C and 342˚C) show the precipitation of anhydrite, caminite and brucite due to their retrograde solubilities. The effluent solutions are greatly depleted in Ca, Mg and SO4.</p> <p> In the seawater-basalt experiments at near-supercritical (400˚C) and subcritical conditions (350˚C), elevated SiO2 concentrations due to glass dissolution are not observed. This is attributed to rapid secondary mineral precipitation. Fluid chemistry and mass balance calculations show almost complete removal of SO4, and in particular, Mg, from the seawater while Ca shows a considerable loss from the rock. Three mineralization fronts were identified: (1) glass dissolution; (2) chloritization; and (3) anhydrite precipitation. In both experiments, there is a switch from chloritization to smectitization. This is accompanied by a decrease in Mg/Fe ratio in smectite. This mineral was also found at the top of both experiments, but its composition was more reflective of the rock.</p> <p>In terms of reactivity, the order of phases from most to least reactive is glass – olivine – clinopyroxene – plagioclase – Fe-Ti oxide. For the aluminosilicate phases this is attributed their respective Al contents. The seawater-basalt experiments also emphasise the fast rate of reaction at which Mg is fixed by the rock, which is conjectured to take less than a few hours.</p> <p>Considering all experiments, the distilled water results show a rock control on fluid chemistry while in the remaining basalt experiments, the chemistry is largely controlled by the fluid.</p> <p>Temperatures calculated using standard Na/K geothermometer did not estimate, in most cases, values close to the experimental temperature. This is due to the inability of the rock to sufficiently adjust the Na/K ratio given the secondary mineral assemblages that form.</p> <p> </p>


2021 ◽  
Author(s):  
◽  
Mauro Passarella

<p><b>To investigate the interaction between fluids and basalt at subcritical, near-supercritical, and supercritical hydrothermal conditions (350-400˚C/500 bar), eight experiments have been conducted. These used a continuous-flow, high temperature and pressure hydrothermal apparatus. The basalt was reacted with three fluids: distilled water; geothermal brine; and natural seawater. Two further experiments used only seawater as a control to determine its behaviour without the influence of basalt.</b></p> <p> With distilled water, the fluid chemistry results show elevated SiO2, K, Cl, SO4, and H2S in solution for the first 12 days of both experiments. This is due to volcanic glass dissolution. After glass was removed, fluid composition was controlled by the remaining rock minerals. At 400˚C, the secondary mineral assemblage at the bottom of the Reactor (fluid entry point) is composed of grossular, wollastonite, anorthite, and chlorite. These results show the effectiveness of distilled water, which lacks any alkali cations, at removing Na and K rapidly from the rock. At the top of the Reactor (fluid exit point) the secondary minerals are anorthite and celadonite. At 350˚C, the secondary mineral assemblage at the bottom is anorthite and chlorite, while celadonite is the dominant secondary mineral at the top. In both experiments, celadonite replaces solely olivine. The formation of celadonite through reaction with distilled water shows that it can be formed by the interaction of deuteric water and basalt without addition of other components.</p> <p> The geothermal brine contains high concentrations of SiO2, K, SO4, Na, Cl and has an acidic pH. At 400˚C, fluid chemistry displays elevated SiO2 concentrations for approximately two weeks due to glass dissolution. At 350˚C, SiO2 concentration is initially high after temperature increase, but decreases gradually over the remainder of the experiment. At 400˚C, the secondary mineral assemblage at the bottom of the Reactor is composed of anhydrite and biotite, while at the top of the Reactor, smectite is the only secondary mineral. At 350˚C, anhydrite and smectite are found at the bottom, while only smectite is found at the top. The lack of biotite at 350˚C suggests this mineral’s precipitation kinetics are too slow to outcompete chlorite precipitation.</p> <p> The seawater-only experiments were conducted as controls to determine its behaviour during heat-up and provide the input solution composition for the seawater-basalt experiments. Both seawater-only experiments (377˚C and 342˚C) show the precipitation of anhydrite, caminite and brucite due to their retrograde solubilities. The effluent solutions are greatly depleted in Ca, Mg and SO4.</p> <p> In the seawater-basalt experiments at near-supercritical (400˚C) and subcritical conditions (350˚C), elevated SiO2 concentrations due to glass dissolution are not observed. This is attributed to rapid secondary mineral precipitation. Fluid chemistry and mass balance calculations show almost complete removal of SO4, and in particular, Mg, from the seawater while Ca shows a considerable loss from the rock. Three mineralization fronts were identified: (1) glass dissolution; (2) chloritization; and (3) anhydrite precipitation. In both experiments, there is a switch from chloritization to smectitization. This is accompanied by a decrease in Mg/Fe ratio in smectite. This mineral was also found at the top of both experiments, but its composition was more reflective of the rock.</p> <p>In terms of reactivity, the order of phases from most to least reactive is glass – olivine – clinopyroxene – plagioclase – Fe-Ti oxide. For the aluminosilicate phases this is attributed their respective Al contents. The seawater-basalt experiments also emphasise the fast rate of reaction at which Mg is fixed by the rock, which is conjectured to take less than a few hours.</p> <p>Considering all experiments, the distilled water results show a rock control on fluid chemistry while in the remaining basalt experiments, the chemistry is largely controlled by the fluid.</p> <p>Temperatures calculated using standard Na/K geothermometer did not estimate, in most cases, values close to the experimental temperature. This is due to the inability of the rock to sufficiently adjust the Na/K ratio given the secondary mineral assemblages that form.</p> <p> </p>


2021 ◽  
Vol 882 (1) ◽  
pp. 012003
Author(s):  
V S H Sujoto ◽  
Sutijan ◽  
W Astuti ◽  
F R Mufakhir ◽  
H T B M Petrus

Abstract The demand of lithium in the global market is experiencing a significant increase. The electric vehicle era is the driving force of this lithium increase phenomenon. Although the demand of lithium continues to increase every year, the available lithium resources are still not able to meet the demand, so that lithium resources with much greater potential are being considered. The main objective of this study is to extract lithium from a primary resource, geothermal brine, with a practical and environmentally friendly method. Research on the extraction of lithium resources from synthetic geothermal brine with a specific lithium composition using the electrodialysis (ED) method has been carried out. The ED device used is provided with electricity and is operated using temperature variations (30°C and 40°C) and variations in electric voltage (2 V and 4 V). The highest flux is achieved at an operating temperature of 40°C and a power supply voltage of 4 V.


2021 ◽  
Author(s):  
Pejman Shoeibi Omrani ◽  
Kaj Van der Valk ◽  
Wim Bos ◽  
Eduard Nizamutdinov ◽  
Laurens Van der Sluijs ◽  
...  

Abstract The electrical submersible pump (ESP) is an essential and critical component in most low-enthalpy geothermal wells where high volumes of hot (up to 120°C) and harsh geothermal brine is required to be transported to the surface. Despite a great deal of knowledge and experience in the design and operation of ESP in the petroleum and water sector, reliability of geothermal ESPs requires further improvement. Frequent failures have been observed that resulted from sub-optimum design, installation and operation of these systems which made the lifetime of them shorter than the expected 5-7 years. In this paper we summarize the typical conditions in low-enthalpy geothermal systems (specifically in the Netherlands) and several observed reliability challenges. Lastly, we will discuss the gaps between the petroleum, water and geothermal practices and identify a list of R&D opportunities to better understand the geothermal ESP failures and improve ESP reliability. Testing ESPs in realistic geothermal conditions and a proper monitoring of the well-ESP system is crucial to improve the reliability of existing ESP designs and can enable the development of new geothermal ESP system designs.


2021 ◽  
Vol 21 (5) ◽  
pp. 1063
Author(s):  
Nur Hayati ◽  
Hanik Humaida ◽  
Dwi Siswanta

Silica scaling is a common problem in geothermal power generation facilities which inhibits electricity generation. In order to provide a solution to this problem, the removal of silicate ions using CPEG-TOMAC (Chitosan-polyethylene glycol–trioctyl methyl ammonium chloride) membrane adsorbent was investigated for geothermal brine from Geo Dipa Energy, Dieng. The process is dependent on contact time, pH, and the concentration of silicate. An adsorption batch study that used adsorbents for the geothermal brine of the Dieng Geo Dipa reactor 28A showed that CPEG TOMAC at pH 6 resulted in an adsorption capacity of 72.6 mg g–1. Furthermore, the adsorption of silicate ions onto the membrane followed pseudo-second-order kinetics and the Freundlich isotherm model.


Geothermics ◽  
2020 ◽  
Vol 87 ◽  
pp. 101863 ◽  
Author(s):  
Jacquelin E. Cobos ◽  
Erik G. Søgaard

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