Next Article in Journal
Quality Assessment and Classification of Feedstock for Bioenergy Applications Considering ISO 17225 Standard on Solid Biofuels
Previous Article in Journal
Microplastic Pollution in Terrestrial Ecosystems and Its Interaction with Other Soil Pollutants: A Potential Threat to Soil Ecosystem Sustainability
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

A Review of Critical Element Concentrations in High Enthalpy Geothermal Fluids in New Zealand

1
GNS Science, Wairakei Research Centre, Taupo 3384, New Zealand
2
GNS Science, Dunedin Research Centre, Dunedin 9016, New Zealand
3
GNS Science, National Isotope Centre, Lower Hutt 5010, New Zealand
*
Author to whom correspondence should be addressed.
Resources 2023, 12(6), 68; https://doi.org/10.3390/resources12060068
Submission received: 27 March 2023 / Revised: 22 May 2023 / Accepted: 23 May 2023 / Published: 29 May 2023

Abstract

:
This review compiles publicly available datasets describing the chemical composition of geothermal fluids from eight wells in the Taupo Volcanic Zone (TVZ) and Ngāwhā, New Zealand. Our review allows previously reported geothermal reservoir water compositions at various locations around the TVZ (and Ngāwhā) to be assessed and compared for the first time. The combined data present a new perspective on potential critical elements of geothermal resources and will be a valuable tool for future research projects and investment opportunities. Composition data were used to estimate the annual flux of different elements in New Zealand geothermal systems. Several elements found in New Zealand geothermal fluids are currently considered ‘critical’ for the transition to a carbon-neutral economy and are present in economically extractable quantities. We estimate that each year, approximately 1100 tons of lithium pass as heat exchange fluids through Wairakei geothermal power station. An overview of the critical elemental capture and extractive potential from New Zealand’s geothermal fields is provided.

1. Introduction

Building a low-carbon energy ecosystem for Aotearoa, New Zealand, will require access to new resources of specific elements and materials. Elements that play an important role in low-carbon future technologies—many of which are classified as ‘critical elements’—are unevenly distributed around the world [1]. Often, ‘critical element’ supply chains (both for mining and processing) are dominated by a few players that are granted a “near-monopoly” in a small number of countries. While global efforts to secure supply chains of critical elements have focused on traditional mineral ore bodies and material recycling, critical elements are known to occur in geothermal fluids in economically extractable quantities [2,3,4,5,6,7,8]. Geothermal fluids used to generate electricity represent a particularly interesting opportunity for critical element extraction, thanks to the existing substantial infrastructure. Although the process of economic recovery of aqueous critical elements presents technical challenges [3,9], it is certainly worth exploring, especially considering the potential added value to producing geothermal power stations [10]. The aim of this review is to extract and compile data from almost 60 years of studies of New Zealand geothermal fluids. This paper offers a comprehensive insight into the composition of New Zealand geothermal fluids and provides potential quantitative extractable estimates of critical element resources. Although some of the geochemical data are dated or were sampled and analyzed using different techniques, they still offer first-order guidance on potential elemental abundances and subsequent extraction opportunities. This is the first study to compile geothermal fluid compositions for such a wide range of elements—previous reviews of geothermal well compositions have focused on the elements of highest abundance and also addressed the most commonly analyzed elements (i.e., Na, K, Ca, Cl, B, SiO2, Li, Rb, Cs, Mg, Au, Ag, and Cu [8].

1.1. Critical Elements

Critical elements are defined as those that are crucial to society for economic growth and/or national security but which are vulnerable to supply disruption (Figure 1) [11]. They are usually in high demand and have no practical substitutes. As such, the elements deemed ‘critical’ change through time due to social, technical, and political changes [12]. Presently, most of the elements classified as ‘critical’ are essential components for clean energy (i.e., solar, wind) and clean technology (i.e., electric vehicles, home battery devices) sectors and are therefore crucial in enabling the move to a global low-carbon economy. There are currently 50 elements and minerals listed as critical in the United States of America (USA) [13]. These are: aluminum, antimony, arsenic, barite, beryllium, bismuth, cerium, caesium, chromium, cobalt, dysprosium, erbium, europium, fluorspar, gadolinium, gallium, germanium, graphite, hafnium, holmium, indium, iridium, lanthanum, lithium, lutetium, magnesium, manganese, neodymium, nickel, niobium, palladium, platinum, praseodymium, rhodium, rubidium, ruthenium, samarium, scandium, tantalum, tellurium, terbium, thulium, tin, titanium, tungsten, vanadium, ytterbium, yttrium, zinc, and zirconium.
In comparison, the European Union defined its own list of critical materials (elemental groups and minerals) [14,15], including many of the elements listed as ‘critical’ by the US Geological Survey (USGS), but also including bauxite, borate, coking coal, natural rubber, phosphate rock, phosphorus, silicon metal, and strontium.
New Zealand does not currently have a list of elements considered ‘critical’ for societal, economic, and/or national security reasons. However, the necessity for the development of such a list has been recognized as a part of a plan to secure affordable resources to meet New Zealand’s future mineral and energy needs. As part of the Ministry of Business, Innovation and Employment’s (MBIE) 2019–2029 Resource Strategy for New Zealand, a list of critical minerals specific to New Zealand is in development [16].

1.2. Extraction of Critical Elements from Geothermal Fluids

Growing demand for carbon-neutral renewable energy is generating an incentive to grow geothermal developments worldwide. New Zealand is no different, and geothermally generated electricity accounts for c. 20% of New Zealand’s total electricity supply, with new field developments still ongoing. In addition to generating electricity, geothermal fluid can also be used as a direct source of heat energy in industrial, commercial, and residential sectors. In Iceland, geothermal heating utilizing geothermal fluids piped into buildings has provided heating and hot water for >90% of all of Iceland’s buildings for more than 20 years [17]. In New Zealand, geothermal heat is used to dry timber, manufacture milk powder, and heat glasshouses for horticultural purposes.
Well-managed geothermal resources are a source of clean, reliable, and sustainable energy. Once geothermal fluid has been extracted from a production well and has been used to generate electricity or supply heat, the energy-depleted fluid is reinjected back into the reservoir through reinjection wells some distance from the production well. The reinjected fluid flows through the fractured reservoir network (i.e., permeable zones in the rock), extracting more thermal energy from the rocks and mixing with the reservoir fluid as it flows back towards the production well [18,19,20,21,22].
In recent years, research has begun to examine the potential for the commercial extraction of various elements from geothermal fluids (Figure 2), (i.e., [3,4,6,23,24]. This new and emerging industry has the potential to develop into a significant multi-million-dollar industry both in New Zealand and internationally. However, multidisciplinary collaborative research is necessary to assist in removing implementation barriers [25]. Despite promising fluid compositions and the substantial volume of geothermal fluid production at numerous geothermal fields in the Taupo Volcanic Zone (TVZ), the additional opportunity for critical element extraction at a commercial scale in New Zealand is yet to be realized for minerals other than silica.

1.3. Recovery of Elements from Geothermal Fluids

The concept of multi-element extraction from geothermal fluid is not new. In the 1960s, extraction of lithium, sodium, and potassium from the Wairakei geothermal field was considered [26]. In the early 1980s, a pilot plant at Wairakei was set up to separate solids (e.g., calcium silicate) from geothermal fluid [10]. Subsequently, over the years, many researchers and engineers have revisited the opportunity for mineral extraction from geothermal fluids [3,5,6,8,9,25,27,28,29,30,31].
Today a sustainable silica extraction plant is in operation at the Ohaaki geothermal power station in New Zealand, with a lithium extraction plant in the pilot stages of operation. In the USA, at Salton Sea, California, three companies are developing chemical processes to extract lithium in economic quantities from geothermal fluids [32]. Similarly, other countries, including the United Kingdom (UK) and Italy, are exploring opportunities to extract elements from geothermal fluids [33,34,35], and in Germany, the first example of battery-grade lithium has already been produced from geothermal fluids [36].

2. New Zealand High-Temperature Geothermal Systems

Historical well water compositions from eight currently operated, high-temperature geothermal fields, Ohaaki, Kawerau, Mokai, Ngatamariki, Ngāwhā, Rotokawa, Tauhara, and Wairakei (Figure 3, with Ngāwhā field in the insert), are compiled. New Zealand’s high-temperature geothermal systems are restricted to the TVZ except for Ngāwhā, which is located in Northland (Figure 3). The TVZ is an active continental volcanic arc/back-arc basin, resulting from subduction of the Pacific Plate beneath the Australian Plate along New Zealand’s North Island [37]. It is a region of active extension and crustal thinning, with high-heat flow and productive rhyolitic volcanism [38,39]. The TVZ extends from Ruapehu in the south to Whakaari/White Island in the northeast and is flanked and underlain by basement metasedimentary rocks (greywacke and argillite) of the Mesozoic Torlesse and Waipapa composite terranes [38,40]. The northern and southern ends of the TVZ are dominated by volcanics of andesitic composition, while the central segment is dominated by rhyolitic compositions [41,42]. Most of the high-temperature geothermal systems are located within rocks of rhyolitic composition, though lithologies are variable (i.e., rhyolitic ignimbrites and lavas interbedded with lacustrine and fluvial sediments [39].
The Ngāwhā geothermal system occurs in the north of the North Island and is hosted within Permian-Triassic basement metasedimentary rocks of the Waipapa Composite Terrane [43]. Quaternary felsic volcanism is proposed as the heat source for the Ngāwhā geothermal system [39].
More than twenty defined geothermal fields have been identified within the TVZ (Figure 3), seven of which are in current use to generate electricity and have geothermal fluid temperatures exceeding 230 °C (Table 1).
Table 1. Maximum reported temperature of geothermal reservoir fluids for geothermal fields considered in this review.
Table 1. Maximum reported temperature of geothermal reservoir fluids for geothermal fields considered in this review.
Wairakei–TauharaKawerauRotokawaNgatamarikiOhaaki–BroadlandsMokaiNgāwhā
Max Temperature280 °C [44]310 °C [45]337 °C [46]>280 °C [47]307 °C [48]>300 °C [44]230 °C [49]

Composition of New Zealand Geothermal Fluids

The composition of New Zealand’s deep geothermal fluids (i.e., high-temperature fluid, which is enriched in chemical components) is reduced, near-neutral pH chloride waters predominantly of meteoric origin with occasional evidence of limited magmatic fluid components [50,51,52]. Geothermal fluid composition is influenced by temperature, pressure, host rock, and mixing between various fluid types [19]. Therefore, the fluid composition of each geothermal field has its own unique chemical signature. The major solutes include Na, Si, K, Al, Fe, Mg, and Al (i.e., rock-forming elements) and magmatic volatiles such as Cl, CO2, and H2S. Fluid interaction with surrounding rocks results in leaching of other elements such as Cs, Rb, or rare earth elements (REE) [8,53]. It is important to note that even if the concentrations of elements in geothermal fluids are quite low (i.e., at ppm to ppb levels), their potential economic value may still be substantial, especially in the context of the large volumes of fluids that are circulated each year through geothermal power stations.
Table 2 shows a compilation of published and unpublished data from the selected New Zealand geothermal fields, showing the elemental concentration (ppm = mg L−1, ppb = µg L−1) of geothermal fluids measured at each site. The data presented in this review were collected and analyzed between 1967 and 2016 by multiple authors (for references, see Appendix A). The data extracted from these reports vary in their analytical techniques and sampling approach, as some samples were collected from different depths and others from separated fluids. Special caution has to be taken for Nd, Sm, Gd, and Er values as these authors reported that some of them were present as contamination in sampling containers [2,8,9,47,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67]. Furthermore, the compiled elemental data may not directly reflect the stable element fluxes for each geothermal system (i.e., element concentrations may vary with time, especially with continued extraction of fluids for geothermal power generation, which may deplete the overall potential critical element resource). Therefore, while the compiled results are indicative only, they constitute a good starting point for understanding and comparing critical element geochemistry of fluids from some New Zealand geothermal fields and provide a foundation for future research.
It is important to note that different elements behave differently within geothermal fluids. Some of the elements can be transported as very soluble species (e.g., B, Cl, K, Na), while others are mostly deposited in the fracture systems and alteration zones beneath the surface (e.g., Fe, Mn). Some elements travel to the surface of geothermal systems and are deposited as precipitates around natural features (i.e., hot springs, geysers, mud pools). Note that precipitation occurs because of changing conditions of the transported fluid from depth to the surface (change in temperature, pressure, pH, Eh). These precipitates can contain a range of elements, such as Au and Ag precipitates or Ga-rich muds, found around natural features of the Rotokawa geothermal system [2] or Au deposits at Waiotapu [57].
When geothermal fluid travels through the pipeline infrastructure of a geothermal power station, it undergoes physical (temperature, pressure) and chemical changes (due to CO2 or H2S degassing, acid-dosing, or use of anti-scalants). These changes increase the mobility of some elements or deposition of others. Elements can be deposited as silica scales, metal sulfides, metal oxides, or alloys (e.g., Au or electrum). These deposits have been reported at wellheads, separators, heat exchangers, two-phase pipelines, and/or reinjection pumps in several geothermal systems [68]. In fact, the major solid by-product in geothermal power generation is silica scale and compounds from pipeline corrosion.

3. Critical Element Abundance in New Zealand’s Geothermal Fluids

The concentration of minor and trace elements in New Zealand’s geothermal fluids ranges from <1 ppt (ng L−1) up to several ppm, depending on the element. Figure 4 plots the highest published concentrations for each of the measured elements in New Zealand’s geothermal fluids (Wairakei, Kawarau, Rotokawa, Mokai, Ohaaki–Broadlands, Ngāwhā, Ngatamariki, and Tauhara) ordered by atomic number (see Table 2 for the range in concentrations and references therein). The data for most of the trace elements should be considered only as qualitative, and some concentrations are close to detection limits (see Table 2).
Zirconium and titanium concentrations are below detection limits (with the exception of Rotokawa field). Ba and Bi have been recorded at low concentrations, in the range of <0.01 to 0.1 ppb. Concentrations of Ga, Ho, Lu, Pr, Sm, Tb, Tm, U, V, and Yb are in the range of <0.1 to 10 ppb, and Cd, Ce, Co, Dy, Er, Eu, Gd, Ge, Au, La, Mo, Hg, Se, Tl, Sn, and Y between <0.1 ppb and 100 ppb. Sb, As, Ce, Cr, Cu, I, Fe, Mg, Pb, Mn, Nd, Ni, P, Ag, Sr, Te, W and Zn concentrations show a wide range of <1 ppb to several ppm, most likely associated with the sampling location and sampling technique. Elements Br, Cs, Ca, Li, and Rb are typically present at >1 ppm levels. Note that downhole samples collected at depth show significantly higher concentrations of some elements, including Ag, Cu, Pb, Cd, Zn, and Ni, when compared to samples collected at the wellhead. This reflects the loss of some trace elements from fluid while flowing upwards, towards the wellbore.
Other major elements are present at high ppm concentrations (Cl, Na, Si, B, and K), with the exception of Ngāwhā where B is the third most abundant dissolved constituent. High B concentration is sourced from the argillite/greywacke basement rock or volcanic source associated with the heat source [69].
Alkali metals Li, Na, K, Rb, and Cs are abundant in New Zealand’s geothermal fluids compared to other elements. TVZ southern geothermal fields, Mokai, Wairakei and Tauhara, are shown to be relatively enriched in these elements in comparison to the eastern geothermal fields at Kawerau, Ohaaki, and Rotokawa. Whereas the alkaline-earth major metals Ca and Mg and trace metals Ba and Sr are at low ppm levels in all fields, with the exception of Ca in Wairakei and Mokai.
The transition metals and metalloids are particularly unevenly distributed. Specifically, the Ohaaki field stands out with low Mn, Ni, Ga, Ge, and Te concentrations and elevated REE and W. Rotokawa’s geothermal fluid is relatively enriched in Mn, Ni, Ga, Te, Ag, and Au but depleted in REE. The differences are related to available transporting complexes, reservoir rocks, temperatures, and most likely amount of magmatic fluid input. More details on these distinctions can be found in [53,70].

Theoretical Quantities of Critical Elements in Geothermal Fluids

Despite the low relative concentrations of many critical elements within New Zealand geothermal fluids, it is worth considering their quantities in the context of the significant volumes of fluids that pass through geothermal power stations annually. The consented annual take for different geothermal fields and the estimated annual element flux are presented in Table 3. Element flux has been calculated for several species and is given based on the highest recorded concentration multiplied by the consented fluid taken for the specific producing geothermal field.
The calculated mass flux indicates both the fluid mass flow and concentration. For example, the greatest SiO2 annual flux has been calculated for the Kawerau geothermal field, despite that field not having the highest contested take. Similarly, at Ngāwhā, boron concentration is so high that annual boron discharge is 9700 t/yr, more than double the next highest discharge from Kawerau.
On the other hand, the Wairakei and Tauhara geothermal fields, with the highest consented fluid mass discharge, have by far the highest total mass of Cl, Na, K, Li, Cs, and Rb flux in comparison to other geothermal fields. Growing demand for lithium has accelerated the exploration of new Li resources, with around 98 million tonnes being available worldwide and 130,000 tonnes being mined in 2022 alone [1]. Therefore, New Zealand’s annual Li mass flux has the potential to constitute about 3% of the current annual world supply. Flux values are particularly interesting for rubidium and cesium, as less than 200,000 tons (each) of these elements were thought to be available in Australia, Canada, China, and Namibia [71]. This suggests that up to 0.29% and 0.27% of the world’s Rb and Cs resources, respectively, could be supplied by environmentally friendly extraction from New Zealand geothermal fluids. While currently these resources may be sub-economic, extraction techniques already exist [72], and the growing demand for these elements can and should accelerate this resource utilization. Moreover, it has been reported that demand for Rb is limited by scarce supply, hence, new resources could lead to expanded commercial applications [73].
Table 3 reveals a notable difference in the potential REE (Nd, Eu, Tb, Dy, and Yb) annual mass discharged for the Wairakei and Ohaaki–Broadlands geothermal fields, as they discharge the greatest amounts of these critical elements. For context, annual production of Nd reported in 2017 was 7300 tons and 400 tons of Eu [3]. Therefore, if the reported REE concentrations are correct, the Wairakei and Ohaaki-Broadlands geothermal fields possess an enormous potential to become a relevant REE supply. Finally, global tungsten production volume for 2021 was 79,000 tonnes [74]. Therefore, the potential annual produced mass from New Zealand geothermal fields equates to around 0.05% of the annual global production. The full table of calculated annual mass flux of all reported elements is available in Appendix B.

4. Concluding Remarks

This review briefly summarizes and consolidates published historical data on critical element concentrations in New Zealand geothermal fluids. The data confirm that most elements currently classified as ‘critical’ are present in measurable quantities. The total flux of various species, in tonnes per year, has been calculated using the geothermal fluid taken for each individual geothermal field. The elemental flux calculations constitute one of the first attempts to quantify the potential extractable critical element resources within New Zealand geothermal fluids.
Our data compilation and analysis highlight significant elemental flux in New Zealand geothermal systems and signals that these elements are not evenly distributed across fields. The highest concentrations and fluxes of Ag, Au, and Te were recorded from the Rotokawa and Mokai fields, while the highest REE concentrations are present in fluids from the Wairakei and Ohaaki-Broadland fields.
Extraction of critical elements from geothermal fluids presents many benefits, in particular, the opportunity to extract these elements in an environmentally benign and sustainable way. Combined element extraction and power generation can also offset the extraction costs. Even if current economic constraints hinder the viability of critical element extraction, this may rapidly change with growing demand for more desirable elements and ongoing research and development in element extraction techniques globally.
Nevertheless, it is important to note that the geothermal well concentrations presented here represent a historical snapshot of the potential for a geothermal system to host critical element resources. Regretfully, this data compilation (and associated knowledge) is mostly outdated, as many of the wells were analyzed more than 20 years ago when laboratory techniques were limited (as modern instruments now have much lower detection limits). To more accurately assess the economic commercialization of a critical element extraction industry from geothermal fluids in New Zealand, more research, including standardized sampling and analysis of fluids from all of New Zealand’s producing high-temperature geothermal fields, is required. New testing will provide more precise elemental flux rates and will enable better correlations between critical element concentrations and the various characteristics of each geothermal system to be made (i.e., influence of reservoir host-rock lithology and other factors on controlling the potentially critical element endowment of geothermal fluids).
Once new data verifying critical element concentrations for each geothermal system have been obtained, further work could include the development or adoption of specific element extraction techniques, studies to assess the life cycle of critical elements in geothermal reservoirs and, therefore, their long-term viability, and finally, an economic assessment for a geothermal critical element extractive industry in Aotearoa-New Zealand.

Author Contributions

Conceptualization, L.S., R.T. and K.R.; methodology, L.S. and R.T.; validation, formal analysis, L.S. and R.T.; investigation, L.S.; resources, data curation, L.S. and R.T.; writing—original draft preparation, L.S.; writing—review and editing, L.S., R.T. and K.R.; supervision, R.T.; project administration, K.R.; funding acquisition, L.S. and R.T. All authors have read and agreed to the published version of the manuscript.

Funding

This project was supported by the New Zealand Ministry of Business, Innovation and Employment (MBIE) through the Strategic Science Investment Fund, New Zealand’s Geothermal Future, grant number C05X1702.

Data Availability Statement

All references to data reported can be found in Appendix A.

Acknowledgments

This work was funded by GNS Science Capability Development Fund (CDF). We are grateful to GNS Staff (Ed Mroczek, Bruce Mountain, Rob Reeves, Isabelle Chambefort and Diane Bradshaw) who shared their knowledge and expertise, along with GEO40 engineers and technical staff. We would also like to thank Stuart Simmons for his time and assistance and Scott Wood for access to his extensive chemical compositions database.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Table A1. New Zealand’s Geothermal Fluid Composition References List.
Table A1. New Zealand’s Geothermal Fluid Composition References List.
ElementSymbolSourceElementSymbolSource
AluminiumAl[9,65]MercuryHg[2,53,54,64]
AntimonySb[53,54,55,64]MolybdenumMo[53,62]
ArsenicAs[53,54,55,64]NeodymiumNd[65]
BariumBa[65]NickelNi[53,56,66]
BismuthBi[56]PhosphorusP[65]
BoronB[8,64,75]PotassiumK[53]
BromineBr[53]PraseodymiumPr[65]
CadmiumCd[53,65,66]RubidiumRb[8,75]
CaesiumCs[8,75]SamariumSm[65]
CalciumCa[9,47]SeleniumSe[53]
CeriumCe[65]SiliconSi[8]
ChlorineCl[8]SilverAg[2,8,53,54,76]
ChromiumCr[53]SodiumNa[8]
CobaltCo[65]StrontiumSr[59,65]
CopperCu[2,8,53,55,66,76]TelluriumTe[53]
DysprosiumDy[65]TerbiumTb[65]
ErbiumEr[65]ThalliumTl[53,55,56,64]
EuropiumEu[65]ThuliumTm[65]
GadoliniumGd[65]TinSn[53,56]
GalliumGa[59,61]TitaniumTi[65]
GermaniumGe[56,59,62]TungstenW[53,56]
GoldAu[8,53,54]UraniumU[65]
HolmiumHo[65]VanadiumV[31,65,66]
IodineI[53,66]YtterbiumYb[65]
IronFe[9,63]YttriumY[65]
LanthanumLa[65]ZincZn[53,62,66,77]
LeadPb[66,77]ZirconiumZr[65]
LithiumLi[8,75]
LutetiumLu[65]
MagnesiumMg[8,65,75]
ManganeseMn[53,63,66]

Appendix B

Table A2. Annual Flux in Tons per Year for Elements Reported in Table 2. Only Maximum Values Have Been Caculated. n.d.—no data.
Table A2. Annual Flux in Tons per Year for Elements Reported in Table 2. Only Maximum Values Have Been Caculated. n.d.—no data.
WairakeiKawerauRotokawaNgatamarikiOhaaki–BroadlandsMokaiTauharaNgāwhā
Aluminium134.13864.11243.034591.3007.3007.300n.d.2.738
Antimony16.27531.4735.49910.2935.60618.133n.d.9.764
Arsenic3312863334556n.d.7
Barium0.00117.48516.7350.0001.4600.146n.d.7.300
Bismuth0.000n.d.0.0000.5040.004n.d.n.d.n.d.
Boron3309454671719787658429549700
Bromine948262273186117n.d.46
Cadmium0.0490.0580.3180.0370.2100.102n.d.0.002
Caesium116.25334.97038.25237.23014.60089.060202.1377.300
Calcium1609.65058.28311.95481.03083.220129.940n.d.50.188
Cerium3.7110.0930.0811.5995.8400.051n.d.0.143
Chlorine178,04559,91526,27420,76117,11151,684169,95113,368
Chromium2.14630.3070.9801.5330.5841.562n.d.0.173
Cobalt1.127n.d.0.29972.2260.1170.000n.d.0.279
Copper214.620146.874473.3690.0008.76058.400n.d.42.888
Dysprosium0.4650.0120.0100.0000.4730.007n.d.0.045
Erbium1.0190.0060.0070.0000.1870.006n.d.0.019
Europium0.6440.0060.0070.0000.1610.004n.d.0.054
Gadolinium2.2180.0120.0100.0000.6860.009n.d.0.060
Gallium0.018n.d.0.1340.0000.009n.d.n.d.n.d.
Germanium7.780n.d.0.0000.0260.058n.d.n.d.n.d.
Gold0.0230.1280.8850.0000.0220.015n.d.0.009
Holmium0.3490.0060.0020.0000.0790.001n.d.0.008
Iodine16.99120.39916.7351182.6004.3803.650n.d.7.300
Iron71.5405.8281.4342.1903.65023.360n.d.0.913
Lanthanum1.6630.0520.0430.0003.4890.023n.d.0.074
Lead2.3252.39019.3170.2890.3073.081n.d.0.119
Lithium11363671891991724231174112
Lutetium0.107n.d.n.d.0.0000.0220.001n.d.0.002
Magnesium0.8940.5830.2391.3140.1460.4382.3322.738
Manganese7.78045.4615.1406.0230.0052.716n.d.1.825
Mercury0.2524.5460.1240.0740.1870.016n.d.0.363
Molybdenum9.1210.7290.3830.2280.1750.438n.d.0.078
Neodymium1.967n.d.0.1240.0003.3290.028n.d.0.121
Nickel46.50116.14410.3520.0310.00336.208n.d.2.327
Phosphorus8.9435.828n.d.0.0002.9201.460n.d.3.650
Potassium16,0976936263040081431711018,970757
Praseodymium0.4200.0170.0100.0000.8470.006n.d.0.022
Rubidium196.73540.79850.2060.00021.90071.540202.1372.738
Samarium0.3580.0170.0240.0000.7010.012n.d.0.037
Selenium0.0001.5150.4540.0440.000n.d.n.d.0.158
Silicon (as SiO2)55,26555,60227,80413,44712,10315,62262,8964207
Silver1.2611.95857.3780.4820.1174.526n.d.0.174
Sodium108,83045,98515,13319,53513,41726,03294,5389517
Strontium8.9435.8284.7820.0004.3801.460n.d.10.950
Tellurium0.4020.22770.2880.0880.0191.372n.d.0.006
Terbium0.340n.d.0.0020.0000.0930.001n.d.0.008
Thallium0.9480.4370.0980.0280.1460.219n.d.0.043
Thulium0.080n.d.0.0000.0000.0250.001n.d.0.003
Tin0.9031.8070.0690.0610.1620.047n.d.0.017
Titaniumn.d.n.d.0.0000.0000.000n.d.n.d.0.000
Tungsten19.6746.4114.5420.8767.0082.774n.d.1.369
Uranium0.0890.0060.0100.0000.0910.004n.d.0.061
Vanadium0.1070.8160.1860.2190.1210.064n.d.0.000
Ytterbium0.3490.0120.0070.0000.1470.010n.d.0.017
Yttrium1.6900.0760.0860.0002.3360.031n.d.0.310
Zinc21.73051.28921.03950.2616.4247.300n.d.1.332
Zirconium0.000n.d.4.6140.0000.0000.000n.d.0.000

References

  1. U.S. Geological Survey. Mineral Commodity Summaries 2023; U.S. Geological Survey: Reston, VA, USA, 2023.
  2. Krupp, R.E.; Seward, T.M. The Rotokawa Geothermal System, New Zealand: An Active Epithermal Gold-Depositing Environment. Econ. Geol. 1987, 82, 1109–1129. [Google Scholar] [CrossRef]
  3. Smith, Y.R.; Kumar, P.; McLennan, J.D. On the Extraction of Rare Earth Elements from Geothermal Brines. Resources 2017, 6, 39. [Google Scholar] [CrossRef]
  4. Simmons, S.F.; Kirby, S.; Verplanck, P.; Kelley, K. Strategic and Critical Elements in Produced Geothermal Fluids from Nevada and Utah. In Proceedings of the PROCEEDINGS, 43rd Workshop on Geothermal Reservoir Engineering Stanford University, Stanford, CA, USA, 12–14 February 2018; pp. 1–12. [Google Scholar]
  5. Stringfellow, W.T.; Dobson, P.F. Technology for the Recovery of Lithium from Geothermal Brines. Energies 2021, 14, 6805. [Google Scholar] [CrossRef]
  6. Bourcier, W.; Lin, M.; Nix, G. Recovery of Minerals and Metals from Geothermal Fluids. In Proceedings of the 2003 SME Annual Meeting, Cincinnati, OH, USA, 24–26 February 2003; p. 18. [Google Scholar]
  7. Neupane, G.; Wendt, D.S. Assessment of Mineral Resources in Geothermal Brines in the US. In Proceedings of the 42nd Workshop on Geothermal Reservoir Engineering Stanford University, Stanford, CA, USA, 13–15 February 2017. [Google Scholar]
  8. Mroczek, E.; Climo, M.; Evans, D. The Composition of High Temperature Geothermal Fluids in New Zealand Producing Geothermal Fields; GNS Science Report 2014/68; GNS Science: Taupo, New Zealand, 2015. [Google Scholar]
  9. Mroczek, E.; Dedual, G.; Graham, D.; Bacon, L. Lithium Extraction from Wairakei Geothermal Fluid Using Electrodialysis. In Proceedings of the World Geothermal Congress 2015, Melbourne, Australia, 19–25 April 2015; p. 6. [Google Scholar]
  10. Shannon, W.T.; Owers, W.R.; Rothbaum, H.P. Pilot Scale Solids/Liquid Separation in Hot Geothermal Discharge Waters Using Dissolved Air Flotation. Geothermics 1982, 11, 43–58. [Google Scholar] [CrossRef]
  11. Schulz, K.J.; DeYoung, J.H., Jr.; Seal, R.R., II; Bradley, D.C. Critical Mineral Resources of the United States—An Introduction; U.S. Geological Survey: Reston, VA, USA, 2017.
  12. AGI. Available online: https://Www.Americangeosciences.Org/Critical-Issues/Critical-Minerals (accessed on 16 March 2023).
  13. U.S. Geological Survey. Department of the Interior. 2022 Final List of Critical Minerals. Federal Register, 24 February 2022; p. 87. [Google Scholar]
  14. Bobba, S.; Carrara, S.; Huisman, J.; Mathieux, F.; Pavel, C. Critical Raw Materials for Strategic Technologies and Sectors in the EU—A Foresight Study. 2020. Available online: https://rmis.jrc.ec.europa.eu/uploads/CRMs_for_Strategic_Technologies_and_Sectors_in_the_EU_2020.pdf (accessed on 25 March 2023).
  15. Blengini, G.A.; Latunussa, C.E.L.; Eynard, U.; Torres de Matos, C.; Wittmer, D.; Georgitzikis, K.; Pavel, C.; Carrara, S.; Mancini, L.; Unguru, M.; et al. Study on the EU’s List of Critical Raw Materials (2020) Final Report; 2020; ISBN 978-92-76-21050-4. Available online: https://www.researchgate.net/publication/344124852_Study_on_the_EU’s_list_of_Critical_Raw_Materials_2020_Final_Report (accessed on 20 March 2023).
  16. New Zealand Government. Responsibly Delivering Value—A Minerals and Petroleum Strategy for Aotearoa New Zealand: 2019–2029; 2019. Available online: https://www.mbie.govt.nz/dmsdocument/7148-responsibly-delivering-value-a-minerals-and-petroleum-strategy-for-aotearoa-new-zealand-2019-2029 (accessed on 25 March 2023).
  17. Ragnarsson, Á. Utilization of Geothermal Energy in Iceland. In Proceedings of the International Geothermal Conference, Reykjavík, Iceland, 14–17 September 2003; pp. 39–45. [Google Scholar]
  18. Gudmundsson, A. Transport of Geothermal Fluids along Dikes and Fault Zones. Energies 2022, 15, 7106. [Google Scholar] [CrossRef]
  19. Chicco, J.M.; Giammanco, S.; Mandrone, G. Multidisciplinary Study of the “Salinelle” of Paternò Mud Volcanoes: Characteristics of the Fluids and Possible Correlations with Mt. Etna Activity. Ann. Geophys. 2020, 63. [Google Scholar] [CrossRef]
  20. Chicco, J.M.; Pierantoni, P.P.; Costa, M.; Invernizzi, C. Plio-Quaternary Tectonics and Possible Implications for Geothermal Fluids in the Marche Region (Italy). Tectonophysics 2019, 755, 21–34. [Google Scholar] [CrossRef]
  21. Parisio, F.; Yoshioka, K. Modeling Fluid Reinjection Into an Enhanced Geothermal System. Geophys. Res. Lett. 2020, 47, e2020GL089886. [Google Scholar] [CrossRef]
  22. Davis, T.; Rivalta, E.; Dahm, T. Critical Fluid Injection Volumes for Uncontrolled Fracture Ascent. Geophys. Res. Lett. 2020, 47, e2020GL087774. [Google Scholar] [CrossRef]
  23. Hall, J.; Climo, M. Geothermal Direct Use in New Zealand: Industrial Heat Park Opportunities; GNS Science Report 2014/17; GNS Science: Taupo, New Zealand, 2015. [Google Scholar]
  24. Toba, A.-L.; Nguyen, R.T.; Cole, C.; Neupane, G.; Paranthaman, M.P. U.S. Lithium Resources from Geothermal and Extraction Feasibility. Resour. Conserv. Recycl. 2021, 169, 105514. [Google Scholar] [CrossRef]
  25. Mroczek, E.; Climo, M.; Carey, B.; Li, Y. Technology Review of Mineral Extraction from Separated Geothermal Water; GNS Science Report 2015/25; GNS Science: Taupo, New Zealand, 2015. [Google Scholar]
  26. Kennedy, A.M. The Recovery of Lithium and Other Minerals from Geothermal Water at Wairakei. In Proceedings of the UN Conference on New Sources of Energy, Rome, Italy, 21–31 August 1961. [Google Scholar]
  27. Harper, R.T.; Thain, I.A.; Johnston, J.H. Towards the Efficient Utilization of Geothermal Resources. Geothermics 1992, 21, 641–651. [Google Scholar] [CrossRef]
  28. Brown, K.; Bacon, L.G. Manufacture of Silica Sols from Separated Geothermal Water. In Proceedings of the World Geothermal Congress, Tohoku, Japan, 28 May–10 June 2000; pp. 533–537. [Google Scholar]
  29. Gordon Bloomquist, R. Economic Benefits of Mineral Extraction from Geothermal Brines. Trans.-Geotherm. Resour. Counc. 2006, 30 II, 579–582. [Google Scholar]
  30. Barton, B. Centre for Environmental, Resources and Energy Law/te Putahi o te Ture tai Ao legal Rights to Minerals in Geothermal Fluids; 2015; ISBN 9780473312893. Available online: https://core.ac.uk/download/pdf/44289146.pdf (accessed on 25 March 2023).
  31. Tong Chua, H.; Sommer, H.; Regenauer-Lieb, K. Mineral Recovery Through Geothermal Desalination. In Proceedings of the 40th New Zealand Geothermal Workshop, Taupo, New Zealand, 14–16 November 2018. [Google Scholar]
  32. Brigham, K. The Salton Sea Could Produce the World’s Greenest Lithium, If New Extraction Technologies Work. Available online: https://www.cnbc.com/2022/05/04/the-salton-sea-could-produce-the-worlds-greenest-lithium.html (accessed on 25 March 2023).
  33. Cariaga, C. Partnership to Explore Geothermal Heating and Lithium Extraction in UK. Available online: https://www.thinkgeoenergy.com/partnership-to-explore-geothermal-heating-and-lithium-extraction-in-uk/ (accessed on 25 March 2023).
  34. Richter, A. Research Permit Granted on Geothermal Lithium Extraction in Italy. Available online: https://www.thinkgeoenergy.com/research-permit-granted-on-geothermal-lithium-extraction-in-italy/ (accessed on 25 March 2023).
  35. Cariaga, C. Cornish Lithium Has Proposed the Drilling of a Research Borehole to Explore the Lithium Potential of Geothermal Waters at Blackwater in Cornwall, England. Available online: https://www.thinkgeoenergy.com/cornish-lithium-proposes-new-geothermal-lithium-project-at-blackwater-uk/ (accessed on 15 March 2023).
  36. Cariaga, C. Vulcan Energy Produces Battery Grade Lithium from Geothermal. Available online: https://www.thinkgeoenergy.com/vulcan-energy-produces-battery-grade-lithium-from-geothermal/ (accessed on 15 March 2023).
  37. Cole, J.W.; Spinks, K.D. Caldera Volcanism and Rift Structure in the Taupo Volcanic Zone, New Zealand. Geol. Soc. Lond. Spec. Publ. 2009, 327, 9–29. [Google Scholar] [CrossRef]
  38. Wilson, C.J.N.; Houghton, B.F.; McWilliams, M.O.; Lanphere, M.A.; Weaver, S.D.; Briggs, R.M. Volcanic and Structural Evolution of Taupo Volcanic Zone, New Zealand: A Review. J. Volcanol. Geotherm. Res. 1995, 68, 1–28. [Google Scholar] [CrossRef]
  39. Rowland, J.V.; Sibson, R.H. Structural Controls on Hydrothermal Flow in a Segmented Rift System, Taupo Volcanic Zone, New Zealand. Geofluids 2004, 4, 259–283. [Google Scholar] [CrossRef]
  40. Mortimer, N.; Rattenbury, M.S.; King, P.R.; Bland, K.J.; Barrell, D.J.A.; Bache, F.; Begg, J.G.; Campbell, H.J.; Cox, S.C.; Crampton, J.S.; et al. High-Level Stratigraphic Scheme for New Zealand Rocks. N. Z. J. Geol. Geophys. 2014, 57, 402–419. [Google Scholar] [CrossRef]
  41. Reyes, A.G.; Christenson, B.W.; Faure, K. Sources of Solutes and Heat in Low-Enthalpy Mineral Waters and Their Relation to Tectonic Setting, New Zealand. J. Volcanol. Geotherm. Res. 2010, 192, 117–141. [Google Scholar] [CrossRef]
  42. Wilson, C.J.N.; Rowland, J.V. The Volcanic, Magmatic and Tectonic Setting of the Taupo Volcanic Zone, New Zealand, Reviewed from a Geothermal Perspective. Geothermics 2016, 59, 168–187. [Google Scholar] [CrossRef]
  43. Cox, M.E.; Browne, P.R.L. Structural Setting of Ngawha Geothermal System, North Island, New Zealand. In Proceedings of the 14th New Zealand Geothermal Workshop, Auckland, New Zealand; 1992; pp. 337–344. [Google Scholar]
  44. Bignall, G.; Milicich, S.; Ramirez, E.; Rosenberg, M.; Kilgour, G.; Rae, A. Geology of the Wairakei-Tauhara Geothermal System, New Zealand. In Proceedings of the World Geothermal Congress, Bali, Indonesia, 25–29 April 2010; pp. 25–29. [Google Scholar]
  45. Milicich, S.D.; Wilson, C.J.N.; Bignall, G.; Pezaro, B.; Bardsley, C. Reconstructing the Geological and Structural History of an Active Geothermal Field: A Case Study from New Zealand. J. Volcanol. Geotherm. Res. 2013, 262, 7–24. [Google Scholar] [CrossRef]
  46. Stevens, M. Rotokawa Joint Venture Limited Evidence for Applicant. Statement of Evidence of Michael Stevens. 2016. Available online: http://ngatiteurunga.weebly.com/uploads/4/1/6/6/41662381/rjv_applicant_evidence_package.pdf (accessed on 25 March 2023).
  47. Horton, T.W.; Atkinson, L.; Oze, C. Hydrothermal Carbonate Geochemistry of the Ngatamariki Subsurface Reservoir, New Zealand. In Proceedings of the Thirty-Seventh Workshop on Geothermal Reservoir Engineering, Stanford, CA, USA, 30 January–1 February 2012; p. 8. [Google Scholar]
  48. Brockbank, K.M.; Bixley, P.F. The Ohaaki Deep Reservoir. In Proceedings of the New Zealand Geothermal Workshop, Auckland, New Zealand, 21–23 November 2011. [Google Scholar]
  49. Burnell, J.; Weir, G.; Kissling, W. Modelling the Ngawha Geothermal Field. In Proceedings of the 38th New Zealand Geothermal Workshop, Auckland, New Zealand, 23–25 November 2016. [Google Scholar]
  50. Henley, R.W.; Ellis, A.J. Geothermal Systems Ancient and Modern: A Geochemical Review. Earth-Sci. Rev. 1983, 19, 1–50. [Google Scholar] [CrossRef]
  51. Hedenquist, J.W. The Thermal and Geochemical Structure of the Broadlands-Ohaaki Geothermal System, New Zealand. Geothermics 1990, 19, 151–185. [Google Scholar] [CrossRef]
  52. Chambefort, I.; Buscarlet, E.; Wallis, I.C.; Sewell, S.; Wilmarth, M. Ngatamariki Geothermal Field, New Zealand: Geology, Geophysics, Chemistry and Conceptual Model. Geothermics 2016, 59, 266–280. [Google Scholar] [CrossRef]
  53. Simmons, S.F.; Brown, K.L.; Tutolo, B.M. Hydrothermal Transport of Ag, Au, Cu, Pb, Te, Zn, and Other Metals and Metalloids in New Zealand Geothermal Systems: Spatial Patterns, Fluid-Mineral Equilibria, and Implications for Epithermal Mineralization. Econ. Geol. 2016, 111, 589–618. [Google Scholar] [CrossRef]
  54. Simmons, S.F.; Brown, K.L. The Fl Ux of Gold and Related Metals through a Volcanic Arc, Taupo Volcanic Zone, New Zealand. Geology 2007, 35, 1099–1102. [Google Scholar] [CrossRef]
  55. Brown, K.L.; Simmons, S.F. Precious Metals in High-Temperature Geothermal Systems in New Zealand. Geothermics 2003, 32, 619–625. [Google Scholar] [CrossRef]
  56. Ewers, G.R.; Keays, R.R. Volatile and Precious Metal Zoning in the Broadlands Geothermal Field, New Zealand. Econ. Geol. 1977, 72, 1337–1354. [Google Scholar] [CrossRef]
  57. Weissberg, B.G. Gold-Silver Ore-Grade Precipitates from New Zealand Thermal Waters. Econ. Geol. 1969, 64, 95–108. [Google Scholar] [CrossRef]
  58. Weissberg, B.G. The Use of Mercury in Geochemical Prospecting in New Zealand. N. Z. J. Geol. Geophys. 1994, 17, 731–745. [Google Scholar] [CrossRef]
  59. Goguel, R. Ultratrace Metal Analysis of New Zealand Geothermal Waters by ICP-MS. In Proceedings of the New Zealand Trace Elements Group Conference, Auckland, New Zealand; 1988. [Google Scholar]
  60. Goguel, R. The Rare Alkalies in Hydrothermal Alteration at Wairakei and Broadlands, Geothermal Fields, N.Z. Geochim. Cosmochim. Acta 1983, 47, 429–437. [Google Scholar] [CrossRef]
  61. Crump, M.E. A New Source of Gallium—Geothermal Muds. In Proceedings of the Australasian Institute of Mining and Metallurgy, New Zealand Branch, 28th Annual Conference, Wairakei, New Zealand, 17–19 August 1994. [Google Scholar]
  62. Koga, A. Germanium, Molybdenum, Copper and Zinc in New Zealand Thermal Waters. N. Z. J. Sci. 1967, 10, 428–446. [Google Scholar]
  63. Sabadell, J.E.; Axtmann, R.C. Heavy Metal Contamination from Geothermal Sources. Environ. Health Perspect. 1975, 12, 1–7. [Google Scholar] [CrossRef] [PubMed]
  64. J McKenzie, E.; L Brown, K.; L Cady, S.; Campbell, K.A. Trace Metal Chemistry and Silicification of Microorganisms in Geothermal Sinter, Taupo Volcanic Zone, New Zealand. Geothermics 2001, 30, 483–502. [Google Scholar] [CrossRef]
  65. Wood, S.A. Behavior of Rare Earth Element in Geothermal Systems; A New Exploration/Exploitation Tool. 2002. Available online: https://www.osti.gov/servlets/purl/792697-iVAzEf/native/ (accessed on 20 March 2023).
  66. Weissberg, B.G.; Browne, P.R.L.; Seward, T.M. Ore Metals in Active Geothermal Systems. In Geochemistry of Hydrothermal Ore Deposits, 2nd ed.; John Wiley & Sons, Inc.: Hoboken, NJ, USA, 1979; pp. 738–782. [Google Scholar]
  67. Krupp, R.E.; Seward, T.M. Transport and Deposition of Metals in the Rotokawa Geothermal System, New Zealand. Miner. Depos. 1990, 25, 73–81. [Google Scholar] [CrossRef]
  68. Reyes, A.G.; Trompetter, W.J.; Britten, K.; Searle, J. Mineral Deposits in the Rotokawa Geothermal Pipelines, New Zealand. J. Volcanol. Geotherm. Res. 2002, 119, 215–239. [Google Scholar] [CrossRef]
  69. Aggarwal, J.K.; Sheppard, D.; Mezger, K.; Pernicka, E. Precise and Accurate Determination of Boron Isotope Ratios by Multiple Collector ICP-MS: Origin of Boron in the Ngawha Geothermal System, New Zealand. Chem. Geol. 2003, 199, 331–342. [Google Scholar] [CrossRef]
  70. Chambefort, I.; Stefánsson, A. Fluids in Geothermal Systems. Elements 2020, 16, 407–411. [Google Scholar] [CrossRef]
  71. Jaskula, B.W. U.S. Geological Survey, Mineral Commodity Summaries, January 2021; U.S. Geological Survey: Reston, VA, USA, 2021.
  72. Christopher, T.D.; Mroczek, E.K. A Review on Rubidium and Cesium Extraction Methods from Geothermal and Radioactive Sourced Materials. 2017. Available online: https://shop.gns.cri.nz/sr_2017-002-pdf/ (accessed on 25 March 2023).
  73. Polyak, D.E. Rubidium. U.S. Geological Survey, Mineral Commodity Summaries; U.S. Geological Survey: Reston, VA, USA, 2009.
  74. Garside, M. Global Tungsten Production Volume 2010–2021. Available online: https://www.statista.com/aboutus/our-research-commitment/913/m-garside (accessed on 15 March 2023).
  75. Giggenbach, W.; Sheppard, D.; Robinson, B.; Stewart, M.; Lyon, G. Geochemical Structure and Position of the Waiotapu Geothermal Field, New Zealand. Geothermics 1994, 23, 599–644. [Google Scholar] [CrossRef]
  76. Brown, K.L.; Webster, J.G.; Christenson, B.W. Precious Metal Sampling at the Ohaaki Geothermal Field. In Proceedings of the Proceeding of the 18th New Zealand Geothermal Workshop, Auckland, New Zealand; 1996; pp. 169–174. [Google Scholar]
  77. Brown, K.L. Gold Deposition from Geothermal Discharges in New Zealand. Econ. Geol. 1986, 81, 979–983. [Google Scholar] [CrossRef]
Figure 1. Examples of the use of some critical elements in green technology (electric car batteries, solar panels) and high-tech electronics (i.e., smartphone batteries, magnets, and screens). The examples above include numerous other critical elements not shown that are essential to their various technologies (e.g., electric vehicles).
Figure 1. Examples of the use of some critical elements in green technology (electric car batteries, solar panels) and high-tech electronics (i.e., smartphone batteries, magnets, and screens). The examples above include numerous other critical elements not shown that are essential to their various technologies (e.g., electric vehicles).
Resources 12 00068 g001
Figure 2. Cartoon highlighting the co-existence of geothermal energy production and critical element extraction from geothermal fluids (i.e., lithium).
Figure 2. Cartoon highlighting the co-existence of geothermal energy production and critical element extraction from geothermal fluids (i.e., lithium).
Resources 12 00068 g002
Figure 3. Location of New Zealand geothermal areas; Ngāwhā in northern New Zealand and the TVZ, as discussed in this report. Fields with fluid compositional data listed in Table 1 are indicated by a red circle and listed in bold.
Figure 3. Location of New Zealand geothermal areas; Ngāwhā in northern New Zealand and the TVZ, as discussed in this report. Fields with fluid compositional data listed in Table 1 are indicated by a red circle and listed in bold.
Resources 12 00068 g003
Figure 4. Comparison of elemental concentration in New Zealand’s geothermal fluids (logarithmic scale). Values shown represent the highest measured concentrations of elements reported by different authors (see references in Appendix A) and are ranked by atomic mass.
Figure 4. Comparison of elemental concentration in New Zealand’s geothermal fluids (logarithmic scale). Values shown represent the highest measured concentrations of elements reported by different authors (see references in Appendix A) and are ranked by atomic mass.
Resources 12 00068 g004
Table 2. Elemental content or range of various geothermal fluids from nine different geothermal fields in New Zealand. For detailed references, see Appendix A.
Table 2. Elemental content or range of various geothermal fluids from nine different geothermal fields in New Zealand. For detailed references, see Appendix A.
ElementWairakeiKawerauRotokawaNgatamarikiOhaaki–BroadlandsMokaiNgāwhā
Aluminium ppm1.50.02–1.10.2–1.8n.d.0.3–0.50.50.3
Antimony19–182480–5401.3–23013–27360–38415–1242125–1070
Arsenic2941–37003120–49001180–140094–4701540–30903227–3850770
Barium ppm< <−0.3<−0.7n.d.<−0.1< 0.8
Bismuthn.d.n.d.n.d.n.d.0.3n.d.n.d.
Boron ppm21–3757–7814.6–302338–6020.5–401063
Bromine ppm5.9–10.63.2–4.51.150.8–1.45.94.3–8.05
Cadmium<−0.550.7–1<−13.30.15–0.370.02–14.4<7<−0.19
Caesium ppm1.30.61.61.716.10.8
Calcium ppm180.5–10.53.50.3–5.75.7–8.95.5
Cerium1.1–41.50.3–1.61.5–3.4n.d.0.4–4000.7–3.56.2–15.7
Chlorine ppm1991102810991441117235401465
Chromium0.3–24120–5200.3–4140–73400.3–1072.5–19
Cobalt<−12.6< <−12.5n.d.<−8.0< 29.6–30.6
Copper<0.2–2400490–2520<0.1–19,8002587–32986000.2–4000750–4700
Dysprosium0.2–5.2<−0.20.2–0.4n.d.<−32.4<−0.51.2–4.9
Erbium<−11.4<−0.10.2–0.3n.d.<−12.8<−0.4<−2.1
Europium0.1–7.2<−0.10.2–0.3n.d.<−11<−0.32.8–5.9
Gadolinium<−24.80.1–0.20.2–0.4n.d.<−47<−0.6<−6.6
Gallium0.2n.d.5.6n.d.0.6n.d.n.d.
Germanium3–87n.d.n.d.n.d.3–4n.d.n.d.
Gold<−0.260.03–2.2<−37< 0.1–1.2<−1.5<−1.0<−1.03
Holmium0.7–3.9<−0.10.1n.d.<−5.4<−0.10.2–0.9
Iodine ppm0.11–0.190.2–0.350.05–0.70.35–0.540.30.81–0.250.7–0.8
Iron ppm0.012–0.8<−0.1<−0.06<−0.10.250.05–1.60.1
Lanthanum0.3–18.60.2–0.90.9–1.8n.d.0.2–2390.4–1.63.2–8.1
Lead4.5–2627–41536–8087.4–13.21.3–210.3–211<−13
Lithium ppm12.76.37.99.111.82912.3
Lutetium<−1.2< < n.d.<−1.5<−0.10.1–0.2
Magnesium ppm0.010.010.010.060.010.030.2–0.3
Manganese0.7–87260–780105–215238–2750.009–0.3250–1860.02–200
Mercury<−2.8244–78<−5.180.73–3.4012.82<−1.11<−39.8
Molybdenum6.7–1026–12.514–169.8–10.41225–300.8–8.5
Neodymium<−22< 1.1–5.2n.d.<−228<−1.9<−13.3
Nickel1–52068–2770.5–4330.5–1.40.1–0.22.9–24800.7–255
Phosphorus ppm0.10.1< n.d.0.1–0.20.10.4
Potassium ppm18011996–1101839848772–83
Praseodymium0.1–4.7<−0.30.2–0.4n.d.<−58<−0.40.7–2.4
Rubidium ppm2.20.72.11.61.54.90.3
Samarium<−4.00.1–0.30.3–1.0n.d.<−480.2–0.8<−4.1
Selenium< 18–2612–190.8–2.0< n.d.17.3
Silicon (as SiO2) ppm61895411639358291070461
Silver ppb<0.1–14.11.4–33.61110–24008–222.7–8248–3100.1–19.1
Sodium ppm1090–121778963389291917831043
Strontium ppm0.10.10.2n.d.0.30.11.2
Tellurium<−4.52–3.9<−29403.4–41.30.2–94<−0.66
Terbium<−3.8< <−0.1n.d.<−6.4<−0.10.2–0.9
Thallium2.5–10.63.0–7.50.9–4.10.4–1.34.1–109.7–150.4–4.7
Thulium<−0.9< < n.d.<−1.7<−0.10.1–0.3
Tin<−10.118–31<−2.92.6–2.80.5–11.1<−3.2<−1.9
Titanium< < < n.d.< < <
Tungsten37–22046–11040–19034–4030–48015–19080–150
Uranium0.1–1.0<−0.10.2–0.4n.d.0.1–6.20.2–0.30.9–6.7
Vanadium<−1.2<−142–7.8< <−8.3<−4.4<
Ytterbium0.1–3.9<−0.20.2–0.3n.d.<−10.10.2–0.70.4–1.9
Yttrium1.0–18.90.3–1.31.8–3.6n.d.0.2–1600.8–2.114–34
Zinc<−243730–880100–8801772–22951–440<−5006–146
Zirconium< < <−193n.d.< < <
At the time of writing this report, to our knowledge, no data were available for: Be, Hf, In, Ir, Nb, Os, Pd, Pt, Re, Rh, Ru, Sc, S, and Ta. <−# below detection limit (to see detection limits refer to Appendix A). n.d.—no data were found. Only a small amount of data was available for Tauhara, hence not listed. Data reported in ppb = ug L−1 otherwise marked as ‘element ppm‘ ppm = mg L−1.
Table 3. Consented annual take (t/yr) for producing geothermal fields in New Zealand and annual flux in tons for selected elements.
Table 3. Consented annual take (t/yr) for producing geothermal fields in New Zealand and annual flux in tons for selected elements.
FiledConsented Annual Take (t/yr)ClNaSiO2KLiBCsRbNdEuTbDyYbW
Wairakei89,425,000178,045108,83055,26516,097113633091161971.970.640.340.470.3519.7
Kawerau58,283,20059,91545,98555,6026936367454635410.000.010.000.010.016.4
Rotokawa23,907,50026,27415,13327,804263018971738500.120.010.000.010.014.5
Ngatamariki21,900,00020,76119,53513,447400819919737n.d0.000.000.000.000.000.9
Ohaaki–Broadlands14,600,00017,11113,41712,103143117287615223.330.160.090.470.007.0
Mokai14,600,00051,68426,03215,622711042358489720.030.000.000.010.152.8
Ngāwhā9,125,00013,368951742077571129700730.120.050.010.040.011.4
Tauhara77,745,000 *169,95194,53862,89618,97011742954202202n.d.n.d.n.d.n.d.0.02n.d.
* Tauhara has been consented for 213,000 t/d, including Tauhara II; however, this consent is not expected to be exercised for several years; n.d.—no data.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Sajkowski, L.; Turnbull, R.; Rogers, K. A Review of Critical Element Concentrations in High Enthalpy Geothermal Fluids in New Zealand. Resources 2023, 12, 68. https://doi.org/10.3390/resources12060068

AMA Style

Sajkowski L, Turnbull R, Rogers K. A Review of Critical Element Concentrations in High Enthalpy Geothermal Fluids in New Zealand. Resources. 2023; 12(6):68. https://doi.org/10.3390/resources12060068

Chicago/Turabian Style

Sajkowski, Lucjan, Rose Turnbull, and Karyne Rogers. 2023. "A Review of Critical Element Concentrations in High Enthalpy Geothermal Fluids in New Zealand" Resources 12, no. 6: 68. https://doi.org/10.3390/resources12060068

APA Style

Sajkowski, L., Turnbull, R., & Rogers, K. (2023). A Review of Critical Element Concentrations in High Enthalpy Geothermal Fluids in New Zealand. Resources, 12(6), 68. https://doi.org/10.3390/resources12060068

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop