Transcript Geothermal Waters of the Taupo Volcanic Zone, New Zealand
Geothermal waters of the Taupo Volcanic Zone, New Zealand Ashley Steffen NDSU Geol 428 Geochemistry 2010
Tectonics and Geology Pivot point between two plate-converging systems South Island, located on Pacific Plate North Island on Australian Place 9 Volcanic Centres, 20 geothermal fields Geothermal environments: steep soil temperature gradients extreme pH highly mineralized soils and waters High production of rhyolite beginning c. 1.23 Ma (Giggenbach, 1994 and Boothroyd, 2009) Fig. 1: Plate tectonics of the New Zealand regionhttp://geosphere.gsapubs.org/
Subducting System of North Island Pacific plated “pulled” down Increase in depth causes increase in temperature and pressure. With the addition of water from the subducting oceanic plate, magma is generated.
Fig. 2: Subduction model http://people.uncw.edu/grindlayn/revabstr_vol.pdf
Thermodynamic Systems Convection system Juvenile vs. meteoric waters http://www.anaspides.net/earth_life_sciences/geothermal_fields_taupo_volcanic_zone_nz.html
Water chemistry of lakes in the Taupo Volcanic Zone, New Zealand Timperley, M. H., and Vigor-Brown, R. J., 1986 Looked at 32 lakes and attempted to classify specific sources of their waters Cold water springs and rivers carrying weathered rock Precipitation Geothermal water Geothermal steam Collected into polyethylene bottles from a depth of .5 at lake center or away from inflows
Table 1
Geothermal waters Geothermal steam Cold spring water
pH
8.3
3.3
Na + K +
1330 0 198 0
Ca 2+
23.0
0
Mg 2+ Cl -
0.18
0 2290 0
SO 4 2-
35.0
148
HCO 3 -
66.0
0 Rhyolite pumice Welded ignimbrite Rhyolite pumice Stream Precipitation 7.2
6.8
6.8
5.2
9.6
8.0
5.1
0.58
1.4
2.7
1.3
0.21
Contributing sources and their major ion concentrations (ppm) (Timperley) 3.0
2.3
2.9
0.14
1.4
1.3
2.9
5.2
1.0
0.084
2.6
1.2
2.4
2.4
1.7
0.55
40.8
27.0
23.1
0
Timperley and Vigor-Brown The 32 Lakes 1.Ngakoro 2. Rainbow North 3. Rotokawa 4. Rotomahana 5. Echo 6. Rotowhero 7. Tarawera 8. Rotoehu 9. Rainbow South 10. Rotorua 11. Rotoma 12. Rotoiti 13. Taupo 14. Rotoaira 15. Okataina 16. Opal 17. Rotongaio 18. Okaro 19. Otamangakau 20. Ngapouri 21. Okareka 22. Emerald 23. Tutaeinanga 24. Rotokawau 25. Rotokakahi 26. Ngahewa 27. Rerewhakaaitu 28. Tikitapu 29. Rotopounamu 30. Tama upper 31. Tama lower 32. Blue Fig. 3: Taupo Volcanic Zone Lakes (Timperley and Vigor-Brown)
Timperley and Vigor-Brown Origins of lakes • Total ion concentration of given lake: ∑[i] l =∑{ [i] p l + [i] g l + [i] s l + [i] h l + [i] w l } • Total concentration due to precipitation ∑ [i] p l [Cl [Cl ] ] p p • Total concentration from weathering by steam ∑ [i] s l = 2 { [SO 4 ] l - [SO 4 ] l s - [SO 4 ] l p - [H + ] l } • Total concentration from geothermal water • Total concentration from weathering by H2CO3 ∑[i] w l = 2 {[HCO 3 ] - [HCO 3 ] l g } ∑[i] g l = { [Cl ]-2[Cl ] p [Cl ] g } ∑[i] g
Timperley and Vigor-Brown Group A: small amounts of metal chlorides -> precipitation is a major contributor Group B: Stream and spring waters -> final products of weathering appreciable proportions of metal sulphates in their dissolved salts do not exceed expected from normal weathering -> may result from titration of HCO 3 in lake by sulphuric acid rather than in catchment Group C: >> metal chlorides, greater than precipitation would contribute -> geothermal waters substantial concentrations of metal sulphates from weathering by sulfuric acid Groups E, D, F: >> metal chlorides, greater than precipitation would contribute -> geothermal waters Lakes not influenced by geothermal waters Low [Cl ] Total cation concentrations “almost equal” [HCO 3 ] + [SO 4 ]
Timperley and Vigor-Brown Results/Findings In conclusion, Timperley and Vigor-Brown found it hard to find exact sources for most lakes.
Reaction of geothermal waters with host rock (EQUILIBRIUM_PHASE) Two waters with different compositions Reacted with rhyolite to see what other minerals might form Reacted at different temperatures to if there were different saturations of the minerals present #1 #2
Typical alkali carbonate waters Geothermal waters (Timperley, 1986)
pH 8 pH 8.3
Cl 57 Na 1330 Na 220 K 198 SiO 175 Ca 23 K 43 Mg .18
HCO 1.2
Cl 2290 SO 3177 SO 35 Ca <1 HCO 66 Concentrations taken from “GEOTHERMAL WATERS: A SOURCE OF ENERGY AND METALS.” Department of Earth Sciences, University of Waikato Li F .6
.3
Reacted along with gases
Composition of rhyolite The QAP Triangle All rhyolites are not the same, and exhibit different ratios of quartz, feldspar, and alkali feldspar, along with variable amounts hornblendes, pyroxenes, and biotite. Minerals used Albite (Sodium plagioclase) NaAlSi 3 O 8 K-feldspar KAlSi 3 O 8 Quartz Biotite SiO 2 KMg 3 AlSi 3 O 10 (OH) California State Polytechnic University Pomona: http://geology.csupomona.edu/alert/igneous/igclass.htm
PHREEQC Interactive 1) Define minerals need for reaction PHASE Biotite formula found in Example 16 Need log k and delta h
PHREEQC Interactive Finding log k and ∆H KMg 3 AlSi 3 O 10 (OH) + H 2+ + H 2 O = K + + 3Mg 2+ + Al(OH) 4 + 3H 4 SiO 4
Mineral/element
For this reaction, log k of K-mica (KAl 3 Si 3 O 10 (OH) 2 ) was used
log k=12.703
For delta h, ∆h for all minerals/elements in reaction KMg 3 AlSi 3 O 10 (OH) H 2+ H 2 O K + Mg 2+ Al(OH) 4 3H 4 SiO 4 ∆H R = ∑ ∆H products - ∆H reactants ∆H R = (-1796.16) – (-1762.46) = -34.7 kcal mol
-1 ∆h (kcal mol -1 )
-1488.2 (Robie and Hemingway, 1984) 0.0
-68.315
-60.32
-111.58
-356.2
-348.3
PHREEQC Interactive
PHREEQC Interactive 2) Define solution SOLUTION 1 Geothermal water (Timperley) temp 100 pH 8.3
pe -6.22
redox pe units ppm density 1 Cl 2290 Na 1330 Alkalinity 66 Mg 0.18
S(6) 35 Ca 23 K 198 water 1 # kg Faraday constant
pe=-6.22
R T Eh=-.059 x 8.3
-1 pe= x -.472
(2.303)(1.98x10
-3 )(398)
3) EQUILIBRIUM PHASE Select/type in desired minerals Biotite phase SI – kept at 0 keeps mineral in saturation, but never dissolution -> May precipitate Decide amount desired for reaction PHREEQC Interactive
PHREEQC Interactive When changing temperatures always change pe (same when changing pH) Done at 100 C and 195 C
Water #2 GAS_PHASE PHREEQC Interactive
PHREEQC Interactive Done at 100 C and 150 C
Results 10 0 -10 -20 -30 -40 -50 -60 Waters from Timperley and Vigor-Brown Precipitating phases Anorthite Aragonite Calcite Gibbsite K-mica Kaolinite SI at 100 C SI at 195 C pH went from 8.3 to 8.1 for 100 C 8.3 to 8.01 for 195 C
Typical alkali carbonate waters
pH Cl Na SiO K HCO SO Ca Li F 8 57 220 175 43 1.2
3177 <1 .6
.3
Concentrations taken from “GEOTHERMAL WATERS: A SOURCE OF ENERGY AND METALS.” Department of Earth Sciences, University of Waikato Water #2 +
Gases
CO 2 H 2 H 2 O H 2 S NH 3
Results -40 -50 -60 -70 -10 -20 -30 20 10 0 Second water composition, with added gases Precipitating phases Anorthite Aragonite Calcite
Dolomite Fluorite
K-mica
Talc
SI at 100 C Si at 150 C Gases
CH4(g) N2(g)
pH: went from 8 to 10.4 at 100 C 8 to 11.3 at 150 C
In conclusion Unfortunately, PHREEQC I is limited in it’s temperature gradient. Temperatures of geothermal systems can reach up to 300 C and higher.
Many other variations in the rock types that occur. Not only rhyolite, but andesite, dacite, and basalt, all with varying degrees on plagioclase, alkali-feldspar, quartz, and other minor (but important) minerals.
Reference • Boothroyd, Ian. Ecological characteristics and management of geothermal systems of the Taupo Volcanic Zone, New Zealand. Geothermics. 2009 Vol. 38, pp. 200-209.
• Graham, I.J., et al. Petrology and petrogenesis of volcanic rocks from the Taupo Volcanic Zone: a review. Journal of Volcanology and Geothermal Research. 1995. Vol. 68, pp. 59-87, • Robie, Richard and Hemingway, Bruce. Heat capacities and entropies of phlogopite (KMg 3 [AlSi 3 O 10 ](OH) 2 ) and paragonite (NaAl Mineralogist, 1984. Vol. 69, pp. 858-868.
2 [AlSi 3 O 10 ](OH) 2 ) between 5 and 900 K and estimates of the enthalpies and Gibbs free energies offormation. American • Timperley and Vigor-Brown. Water chemistry of lakes in the Taupo Volcanic Zone, New Zealand. New Zealand Journal of Marine and Freshwater Research, 1986. Vol. 20, pp. 173-183.