Abstract
The equilibrium partitioning of Na and K between alkali feldspar and NaCl–KCl salt melt was determined at 800 \(^\circ\)C, 850 \(^\circ\)C, 900 \(^\circ\)C, 950 \(^\circ\)C and 1000 \(^\circ\)C and close to ambient pressure. Four different natural gem-quality alkali feldspars with low degree of Al–Si ordering covering the range from orthoclase to high sanidine and with slightly different minor element concentrations were used as starting materials. The partitioning curves obtained for the four feldspars are indistinguishable indicating that Na–K partitioning independent of the differences of Al–Si ordering state and minor element concentrations existing amongst these feldspars. A sub-regular two parameter Margules type solution model was fitted to the partitioning data, and the excess Gibbs energy describing the thermodynamic non-ideality of the alkali feldspar solid-solution and the respective Margules parameters \(W_{\text {g}\text {K}}\) and \(W_{\text {g}\text {Na}}\) including their temperature dependence expressed as \(W_g=W_h-TW_s\) were determined:
The corresponding solvus has a critical temperature slightly above 650 \(^\circ\)C and is well comparable with earlier direct experimental determinations of the low-sanidine-albite solvus curve. Comparison of the vibrational excess entropy determined from low-temperature heat capacity measurements with the total excess entropy derived from the temperature dependence of the excess Gibbs energy yields a negative configurational contribution to the excess entropy pointing towards short-range Na–K ordering on the alkali site.
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Introduction
Feldspar is the most abundant mineral in Earth’s crust. The composition of feldspar with respect to its major components may be described in the ternary system CaAl\(_2\)Si\(_2\)O\(_8\)– NaAlSi\(_3\)O\(_8\)–KAlSi\(_3\)O\(_8\). The latter two components define the composition space of alkali feldspar, which is a solid-solution between the albite (NaAlSi\(_3\)O\(_8\)) and K-feldspar (KAlSi\(_3\)O\(_8\)) end-members. In the crystal structure of alkali feldspar, Al and Si are tetrahedrally coordinated by four oxygen ions forming a framework of corner sharing AlO\(_4\) and SiO\(_4\) tetrahedra. The alkali cations occupy large, irregularly coordinated cavities in the tetrahedral framework. Four non-equivalent tetrahedral sites are discerned: T\(_1\)m, T\(_1\)o, T\(_2\)m and T\(_2\)o. In disordered alkali feldspar Al\(^{3+}\) and Si\(^{4+}\) are randomly distributed over all four tetrahedral sites. Preferential partitioning of Al\(^{3+}\) on to the T\(_1\) sites relative to the T\(_2\) sites, where T\(_1\) = T\(_1\)m + T\(_1\)o and T\(_2\) = T\(_2\)m + T\(_2\)o, and finally, preferential partitioning of Al\(^{3+}\) on T\(_1\)o over T\(_1\)m leads to successively more ordered configurations. We adopt the scheme of Ribbe (1983) for the classification of alkali feldspars with different states of Al–Si ordering. For details please refer to the Supplementary Information.
At high temperatures - above about 650 \(^\circ\)C for Al–Si-disordered and above about 900 \(^\circ\)C for ordered alkali feldspar - a continuous solid-solution exists between the Na and K end-members. Towards lower temperatures a miscibility gap opens due to the thermodynamic non-ideality of the alkali feldspar solid-solution. The thermodynamics of the alkali feldspar solid-solution has been addressed by several authors. Direct determinations of the alkali feldspar solvus have been provided by Bachinski and Müller (1971) for ordered alkali feldspars corresponding to the low-albite - microcline series and by Luth and Tuttle (1966), Smith and Parsons (1974), Lagache and Weisbrod (1977) and Parsons (1978) for disordered, topochemically monoclinic alkali feldspars. High pressure solvus experiments in the range of 9 to 15 kbar were provided by Goldsmith and Newton (1974). Ion exchange experiments between alkali feldspar and aqueous solutions were performed at 200 MPa by Orville (1963). The Na–K partitioning between alkali feldspar and (K, Na) Br or (K, Na) Cl salt melt were determined for the low-albite - microcline series by Delbove (1975) and for the analbite - sanidine series, high sanidine after Ribbe (1983), and the adularia (orthoclase) based series by Hovis et al. (1991) and by Neusser et al. (2012).
The enthalpies of the alkali feldspar solid-solution series prepared by cation exchange from alkali feldspar starting materials with different Al–Si ordering states were determined by solution calorimetry (Hovis 1988, 2017), and the vibrational entropies of alkali feldspar solid-solutions were determined from low-temperature calorimetric heat capacity measurements for disordered alkali feldspars of the analbite-sanidine series by Haselton et al. (1983) and for the low-albite - microcline series by Benisek et al. (2015). The compositional dependence of molar volumes of the alkali feldspar solid-solution was determined from powder and single crystal X-ray diffraction data (Orville 1967; Waldbaum and Thompson 1968; Kroll et al. 1986; Hovis 2017).
The current status of knowledge on the thermodynamic mixing properties of the alkali feldspar solid-solution can be summarised as (Hovis 2017): (i) The alkali feldspar solvus is asymmetric with the critical composition between \(X_\text {K}\) = 0.3 and 0.4, where \(X_\text {K}\) is the site fraction of K on the alkali site. (ii) The critical temperature of the alkali feldspar solvus increases with increasing Al–Si ordering. (iii) Accordingly, the excess Gibbs energy, \(g^{\text {ex}}\), is asymmetric with the maximum at \(X_\text {K}\) between 0.38 and 0.44 and maximum values of \(g^{\text {ex}}\) in the range of 3.0–3.5 kJ/mol. (iv) The vibrational excess entropy of mixing \(s^{\text {ex vib}}\) obtained from calorimetric data is higher than the total excess entropy \(s^{\text {ex}}\) of mixing obtained from phase equilibrium data implying the presence of negative excess configurational entropy \(s^{\text {ex,con}}\), which may arise from short range ordering or clustering of Na\(^+\) and K\(^+\) on the alkali sites.
This understanding was derived from combining information from different types of phase equilibrium experiments as well as solution and low-temperature calorimetry measurements. The basic data have been obtained from different feldspars with different Al–Si ordering and trace element contents, both characteristics are partially unknown for the different experiments. Moreover, solvus curves were determined at different pressures, using different starting materials and different experimental techniques and may not be fully comparable.
Thus, despite numerous studies, knowledge of the thermodynamics of the alkali feldspar solid-solution is still limited, and considerable uncertainty with regard to the thermodynamic mixing properties has remained. In this study, we determined the Na–K equilibrium partitioning between natural gem-quality alkali feldspar and NaCl–KCl salt melt under close to ambient pressure and at five different temperatures. We used four different alkali feldspars with slightly different minor and trace element compositions and Al–Si ordering as starting materials applying the exact same experimental procedure for each sample. This ensures direct comparability of the results from the different feldspars and identification of the impact of the degree of Al–Si order and of minor element contents on the excess Gibbs energy. Moreover, it allows for determining \(s^{\text {ex}}\) from the temperature dependence of \(g^{\text {ex}}\) and to obtain \(s^{\text {ex,con}}\) from the difference between \(s^{\text {ex}}\) and \(s^{\text {ex,vib}}\), which was determined for two of the investigated feldspars by low-temperature heat capacity measurements.
Methods
Starting material
Four different K-rich alkali feldspars were used as starting materials: Madagascar Orthoclase (M) (actually low sanidine) from Itrongay, Madagascar, Volkesfeld Sanidine (V) from the Eifel, Germany, Zillertal Adularia (Z) from Zillertal, Austria, and Zinggenstock Adularia (Zg) from Guttannen, Switzerland. All four feldspars are homogeneous and featureless under the light and scanning electron microscope. Madagascar Orthoclase is yellow and Volkesfeld Sanidine greyish-brown, both are transparent. Zillertal Adularia and Zinggenstock Adularia are milky white, 1 mm thick pieces are translucent and colourless (see Fig. S1). For all four feldspars major and trace element concentrations, lattice parameters and the state of Al–Si ordering were determined. For details see the (Fig. S3 and Table S2).
Experimental procedure
Each feldspar was crushed to a powder and sieved. The 63–100 \(\mu\)m fraction was used for the partitioning experiments. About 15 mgs of feldspar powder was mixed with NaCl and KCl salt, where the amount of salt was chosen so that a 40:1 molar proportion of the alkali cations in the salt relative to the feldspar and a certain KCl mole fraction \(X_\text {KCl}\) in the salt was obtained. For details please refer to the Supplementary Information.
For each feldspar and each temperature 12–15 different salt compositions were used to constrain the partitioning over the entire compositional range of alkali feldspar. The salt-feldspar mixtures were then sealed in evacuated quartz glass tubes, shaken for a better mixing of feldspar and salt and kept at 800 \(^\circ\)C, 850 \(^\circ\)C, 900 \(^\circ\)C or 950 \(^\circ\)C for 35 days or at 1000\(^\circ\)C for 28 days in box furnaces at close to atmospheric pressure. Different run durations had been tested beforehand to determine the time needed for complete compositional homogenization throughout the feldspar grains. In addition, experiments were run for each feldspar at 1000 \(^\circ\)C for 28 days and at 900\(^\circ\)C for 35 days to check via pXRD analyses, to what extent the state of Al–Si ordering changes during annealing.
After the exchange experiments, the samples were quenched in cold water, and the glass tubes were checked for tightness. Those which had remained tight after quenching were opened and rinsed with purified water to separate the feldspar powder from the salt. The feldspar powder was then mounted in phenolic resin with graphite filler, polished and carbon coated for electron probe micro analysis (EPMA). All experimental runs are listed in Table 2.
EPMA and ICP-MS analysis
All samples were analysed with a Cameca SX Five electron probe micro analyser (EPMA) at the Department of Lithospheric Research, University of Vienna. 15 kV acceleration voltage and 20 nA beam current were applied, and each element was calibrated on natural mineral standards. The beam was defocused to 6 μm diameter to minimise sample damage and loss of sodium through evaporation. Trace element concentrations were analysed using inductively coupled plasma mass spectrometry (ICP-MS, Agilent 7500) at the Institute of Earth Sciences, University of Graz (Austria). For details please refer to the Supplementary Information.
pXRD
Powder X-ray diffraction (pXRD) was performed on the starting material and on feldspar that was annealed at 900 \(^\circ\)C for 35 days and shifted to different compositions to analyse changes in Al–Si order with thermal annealing and with cation exchange. For the analyses, the feldspar powder was further ground to smaller grain sizes to reduce texture effects. The pXRD measurements were carried out using CuK\(\alpha\) radiation on a Philips PW3020 diffractometer at the Department of Mineralogy and Crystallography, University of Vienna. Rietveld refinement was employed for extracting lattice parameters using the TOPAS-6 software.
Relaxation calorimetry
The heat capacities of 14 samples along the sanidine - high-albite solid solution series prepared from V and of five samples prepared from M were measured in the temperature range of 2–300 K by relaxation calorimetry using a Physical Property Measurement System (PPMS) by Quantum Design at Salzburg University. To this end, 10–20 mg milligrammes of feldspar powder with grain size 100–200 μm were compacted and wrapped into a thin Al foil, pressed into discs and loaded into the calorimeter. Heat capacities between 2 and 300 K were then measured at 60 logarithmically spaced temperature set points in triplicate. For details on the calorimetric measurements the reader is referred to Dachs and Bertoldi (2005).
Thermodynamic analysis of partitioning data
For the exchange of Na and K between alkali feldspar and NaCl-KCl salt melt, the exchange reaction
may be written, where (s) and (liq) indicate solid and liquid phases, respectively. Equilibrium partitioning of Na and K between feldspar and salt melt requires (Thompson and Waldbaum 1968)
where \(\Delta _rg^0\) is the Gibbs energy change of the reaction amongst the end members, \(X_\text {Na}\), \(X_\text {K}\) are the site fractions of Na and K on the alkali site of the feldspar and \(X_\text {NaCl}\), \(X_\text {KCl}\) are the mole fractions of NaCl and KCl in the salt melt. The \(\gamma _i\) parameters are the respective activity coefficients. Based on an asymmetric Margules model (Margules 1895; Thompson 1967) the latter can be described as
where A and B refer to K and Na for the alkali feldspar and to KCl and NaCl for the salt melt. For KCl–NaCl salt melt Margules parameters \(W_{\text {g}\text {KCl}}\) and \(W_{\text {g}\text {NaCl}}\) are available from Hersh and Kleppa (1965) and Yin et al. (2020). At the temperatures of interest, the non-ideality of the salt melt is minute, and partitioning curves calculated with ideal mixing in the salt melt yield slightly better fits to the measured feldspar compositions than when non-ideality in the salt melt is considered. Therefore, for extracting Margules parameters for the feldspar mixing model, \(\gamma _\text {KCl}\) and \(\gamma _\text {NaCl}\) in Eq. (2) were set to unity. Inserting Eq. (3) into Eq. (2) yields
This equation must hold for the Na–K partitioning of every feldspar - salt-melt pair. Each partitioning experiment yields the compositions of salt and feldspar that coexist in equilibrium at a given temperature, and only the two Margules parameters and \(\Delta _rg^0\) are the unknowns. We used the equilibrium partitioning data from 40 to 60 feldspar-melt pairs for each temperature and applied the least square method to simultaneously satisfy the respective 40–60 equations Eq. (4) to obtain the best-fit \(W_{\text {g}\text {K}}\) and \(W_{\text {g}\text {Na}}\) parameters and \(\Delta _rg^0\) for each temperature.
The corresponding partitioning curves are obtained from rearranging Eq. (4) to
and inserting the best-fit Margules parameters and \(\Delta _rg^0\) for each temperature. Only the results obtained based on the assumption of ideal mixing in the salt melt are presented and discussed here. For comparison, results obtained from calculations including non-ideal mixing in the salt melt are shown in the Supplementary Information (Fig. S5). In addition, \(\Delta _rg^0\) was calculated from thermodynamic data of Holland and Powell (1998), upgrade 5.5 (ds55) using PerpleX (Connolly 2005), which yielded values for \(\Delta _rg^0\), which are close to those obtained from the least square fit and, accordingly, almost identical partitioning curves. The \(\Delta _rg^0\) values calculated from the dataset of Holland and Powell (2011) (ds633) are, however, not suited for reproducing our partitioning data potentially indicating a disconnection between silicate and halide data in the latest version of the thermodynamic data set (see Fig. S6 and Table S3).
The \(W_{\text {g}\text {Na}}\) and \(W_{\text {g}\text {K}}\) parameters obtained for the different temperatures show a moderate decrease with increasing temperature (Fig. 1). Making use of the relation (Thompson and Waldbaum 1968; Thompson 1967)
the \(W_{\text {h}\text {K}}\), \(W_{\text {s}\text {K}}\), \(W_{\text {h}\text {Na}}\) and \(W_{\text {s}\text {Na}}\) parameters were extracted from linear fits of \(W_{\text {g}\text {Na}}\) and \(W_{\text {g}\text {K}}\) versus temperature. The resulting excess molar enthalpy and molar entropy functions were obtained from (Thompson 1967; Thompson and Waldbaum 1968)
The corresponding solvus curve was calculated based on
using Gibbs energy minimisation. It must be noted, that the run products are likely metastable with respect to their Al–Si ordering state, as attainment of equilibrium Si–Al distribution is not very likely to occur over the time scales of the cation exchange experiments.
Thermodynamic analysis of calorimetric data
Heat capacities from low-temperature calorimetric measurements were used to calculate the vibrational entropy \(s^\text {vib}\) at reference temperature (298.15 K) according to the relationship
where \(c_P\) is the heat capacity at constant pressure. The excess vibrational entropy \(s^\text {ex,vib}\) of the solid-solution series is obtained from subtracting the vibrational entropy of an ideal solution \(s^\text {vib,id}\) from the measured \(s^\text {vib}\)
where \(s^\text {vib,id}\) is the weighted average of the end-member vibrational entropies.
Results
Mineral chemistry
The major and trace element compositions of the feldspar starting materials are given in Table 1. All four feldspars are K-rich and generally contain very little Ca. Madagascar Orthoclase contains 1.27 wt% Fe\(_2\)O\(_3\), which corresponds to 0.044 a.p.f.u. Fe\(^{3+}\) on the T-site (Coombs 1954; Hofmeister and Rossman 1984). V, Z and Zg contain Ba (M: 765 ppm, V: 6559 ppm, Z: 6952 ppm Zg: 4595 ppm) and Sr (M: 49 ppm, V: 1355 ppm, Z: 584 ppm Zg: 901 ppm). M has some Ti (233 ppm), all other element concentrations are \(\ll\) 100 ppm. Full mineral chemical analyses are available in the Supplementary Information (Table S2).
Al–Si ordering state
The lattice parameters obtained from pXRD are shown in Table S1. All feldspars are monoclinic with space group C2/m, except for samples that were shifted to X\(_\text {K}<0.3\) or to X\(_\text {K}<0.4\) for Zg adularia, which are metrically triclinic with space group \(C\overline{1}\). The state of Al–Si ordering was determined from the ratio b/c\(^*\) using the equations for \(2t_1\) from Kroll and Ribbe (1987) for monoclinic or triclinic feldspars, respectively. The value \(t_1\) indicates the proportion of the Al-ions on each of the T1 sites where \(t_1\)=0.25 represents fully disordered and \(t_1\)=0.5 fully ordered Al–Si. The respective values for \(2t_1\) are given in Table S1 and are shown in Fig. S3 in the Supplementary Information. The terms high sanidine (HS), low sanidine (LS), and orthoclase (OR) are used in the following as defined by Ribbe (1983) with HS: \(0,5<2t_1<0,666\); LS: \(0,666<2t_1<0,74\); OR: \(0,74<2t_1<1\). Out of the four starting materials, Volkesfeld Sanidine is the most disordered (high sanidine) followed by Madagascar Orthoclase (low sanidine), Zinggenstock and finally Zillertal Adularia (both orthoclase).
Comparison between the starting material and material annealed at 900 \(^\circ\)C and at 1000 \(^\circ\)C for 35 days reveals a systematic increase of Al–Si-disorder during heat treatment (see Table S1 and Fig. S3). Annealing at 900 \(^\circ\)C produced limited disordering with changes of 2\(t_1\) from 0.689 to 0.673 for M, from 0.611 to 0.603 for V, from 0.874 to 0.842 for Z, and from 0.838 to 0.800 for Zg (see Table S1). The changes in Al–Si ordering state are independent of whether annealing occurred isochemically or was accompanied by cation exchange, and the cation exchange series plot along lines of constant 2\(t_1\) in Fig. S3. Annealing at 1000 \(^\circ\)C produced substantial disordering so that all feldspars changed to high sanidine with 2\(t_1\) of 0.579 for Z, 0.646 for Zg, 0.524 for M, and 0.556 for V. Although the feldspars become metrically triclinic when shifted towards Na-rich compositions (see Tab. S1), they remain topochemically monoclinic irrespective of the annealing temperature.
Thermodynamic mixing properties
Excess Gibbs energy of mixing from Na–K partitioning
The compositions of melt, \(X_\text {KCl}{}\), feldspar, \(X_\text {K}{}\), pairs after cation exchange are plotted in Fig. 2. Despite the 40:1 molar ratio for alkali cations contained in melt and feldspar, the melt undergoes a slight change in its composition during the experiments due to the requirement of mass balance in a closed system. For determining the partitioning of Na–K between melt and feldspar the melt compositions were corrected accordingly (see Fig. S4 in the SI). For each feldspar-melt pair the 1\(\sigma\) standard deviation of the feldspar composition obtained from 5–10 EPMA measurements performed on each sample is indicated. For experiments at 800 \(^\circ\)C, the 1\(\sigma\) bars for feldspar compositions are significantly larger than for the experiments performed at 850 \(^\circ\)C, 900 \(^\circ\)C, 950 \(^\circ\)C and 1000 \(^\circ\)C indicating incomplete equilibration at 800 \(^\circ\)C. Shifting K-rich feldspars to Na-rich composition is accompanied by a strongly anisotropic contraction of the crystal structure. Typically, this leads to fracturing, when the compositional shift exceeds about 15 mole% (Neusser et al. 2012; Scheidl et al. 2013; Petrishcheva et al. 2019; Abart et al. 2022). Through this, new surfaces are generated, which enhance melt-feldspar cation exchange. As a result, the Na-rich feldspars are equilibrated relatively well. As all starting materials are relatively K-rich, only small shifts are required to produce the desired compositions on the K-rich side, which are facilitated merely by intracrystalline Na–K interdiffusion. When the starting materials are shifted to intermediate compositions, the compositional shifts may be too small to induce fracturing, and feldspar-melt equilibrium partitioning is the most difficult to attain. Indeed, the largest compositional variations indicating the least extent of equilibration is observed for Z and Zg shifted to intermediate compositions. After cation exchange at 800 \(^\circ\)C M and V appear to be well equilibrated with the salt melt, whereas Z and Zg don’t. This difference rather has kinetic than thermodynamic reasons and for the 800 \(^\circ\)C experiments only the partitioning curves obtained for M and V were considered in the thermodynamic analysis.
The partitioning curves produced from cation exchange at 800 \(^\circ\)C for M and V and at 850 \(^\circ\)C, 900 \(^\circ\)C, 950 \(^\circ\)C and 1000 \(^\circ\)C for all four feldspars are indistinguishable (see Fig. 2). In the thermodynamic analysis we therefore did not discriminate between the partitioning curves obtained for the different feldspars. All melt-feldspar pairs obtained for a given temperature were used to extract the corresponding Margules parameters in a single fitting run. Hovis et al. (1991) and Hovis (2017) suggested to restrict the analysis to feldspar compositions to within the range \(0.07<X_\text {K}<0.91\) since uncertainties for near-end-member compositions are high, and including such compositions could potentially distort the results. Nonetheless, in our study the entire compositional range was used for determining the Margules parameters, as restricting the analysis to feldspar compositions of \(0.07<X_\text {K}<0.91\) did not have any effect on the results. The Margules parameters obtained from fitting Eq. (4) to the partitioning data are given in Table 2, and the corresponding partitioning curves are shown as solid lines in Fig. 2.
The uncertainties given for \(W_{\text {g}\text {K}}\) and \(W_{\text {g}\text {Na}}\) in Table 2 and illustrated in Fig. 1 are standard deviations obtained from selecting feldspar compositions randomised according to mean and standard deviation as determined from EPMA analysis and calculating Margules parameters for each choice of compositions. For details refer to the Supplementary Information.
Even if the \(W_{\text {g}\text {K}}\) and \(W_{\text {g}\text {Na}}\) parameters have considerable associated uncertainties, the mean values indicate a decreasing trend with increasing temperature for both the \(W_{\text {g}\text {K}}\) and \(W_{\text {g}\text {Na}}\) parameters (Fig. 1). The solid lines represent the linear least square fits with slopes \(W_{\text {s}\text {K}}\), \(W_{\text {s}\text {Na}}\), and intercepts \(W_{\text {h}\text {K}}\) and \(W_{\text {h}\text {Na}}\) (Eq. (6)), respectively. The \(W_\text {h}\) and \(W_\text {s}\) parameters were used to calculate \(h^{ex}\), \(s^{ex}\) and \(g^{ex}\), which are shown in Fig. 3 together with literature data (see figure caption for details).
Low-temperature heat capacity measurements
The excess vibrational entropy obtained from heat capacity measurements by low-temperature calorimetry of 14 samples with different \(X_\text {K}\) of the solid-solution prepared from V is shown in Fig. 4. The excess vibrational entropy is positive over the entire compositional range with a maximum of about 2 J\(\cdot\)mol\(^{-1}\cdot\)K\(^{-1}\). The same two parameter sub-regular mixing model as used for fitting \(g^\text {ex}\) was used for obtaining the \(W_\text {s}^\text {vib}\) parameters from the \(s^\text {ex,vib}\) data by least square fitting, the best-fit \(W_\text {s}^\text {vib}\) parameters are given in Table 3. The \(s^\text {ex,vib}\) curve is nearly symmetrical with respect to composition with the maximum at \(X_\text {K} = 0.4\). Based on the notion that excess entropy is the sum of the vibrational and the configurational contribution, \(s^\text {ex} = s^\text {ex,vib} + s^\text {ex,con}\), the configurational contribution, \(s^\text {ex,con}\), to the excess entropy can be obtained by subtracting \(s^\text {ex,vib}\) from \(s^\text {ex}\). The \(W_{\text {s}\text {K}}^{con}\) and \(W_{\text {s}\text {Na}}^{con}\) parameters obtained this way are given in Table 2, and the \(s^{ex,con}\) curve is shown in Fig. 3.
Discussion
The partitioning data depicted in Fig. 2 are reproduced very well by the calculated partitioning curves indicating that the chosen two parameter Margules model is well suited for describing the thermodynamic non-ideality of the alkali feldspar solid-solution. Qualitatively, non-ideality of the alkali feldspar solid-solution can be inferred from the fact that the partitioning curves show an inflection point. Given that the salt-melt has practically ideal thermodynamic mixing properties at the temperatures of the cation exchange experiments (Hersh and Kleppa 1965; Yin et al. 2020), an inflection point in the partitioning curves is an unambiguous indication for non-ideality of the alkali feldspar solid-solution. With increasing temperature, the slope of the partitioning curve at the inflection point increases indicating decreasing non-ideality of the feldspar solid-solution with increasing temperature.
The fact that partitioning at a given temperature is similar for all four feldspars indicates that equilibrium element partitioning between alkali feldspar and NaCl–KCl salt melt is independent of the Al–Si ordering state and of the minor and trace element compositions over the ranges covered by the four feldspar starting materials and the corresponding run products. Through the large number of partitioning data considered for extraction of the Margules parameters at each temperature the \(W_{\text {g}\text {Na}}\) and \(W_{\text {g}\text {K}}\) parameters are well constrained. The 1\(\sigma\) standard deviations indicated in Fig. 1 were obtained from multiple fitting runs, where for successive fitting runs each feldspar composition was calculated from Montecarlo experiments based on the mean value and standard deviation obtained from replicate EPMA measurements of the respective feldspar. Comparison with literature data as shown in Fig. 3a reveals good agreement between \(h^\text {ex}\) derived from our partitioning experiments and the results from solution calorimetry. The latter show increasing \(h^\text {ex}\) and increasing asymmetry of the \(h^\text {ex}\) curve with increasing Al–Si ordering state. The \(h^\text {ex}\) derived from our study is close to \(h^\text {ex}\) of disordered feldspars as given by Hovis (1988); Hovis et al. (1991) and Hovis (2017).
Previous studies that covered a broad range of Si–Al ordering states ranging from the fully ordered low-albite microcline series to the fully disordered monalbite - sanidine series, found that the alkali feldspar solid-solution becomes increasingly more non-ideal with increasing state of Si–Al ordering (see Fig. 3). This is in line with experimentally determined two-feldspar equilibrium phase relations, which reveal immiscibility up to 900 \(^\circ\)C (Bachinski and Müller 1971) for ordered feldspars, and up to about 600 \(^\circ\)C for disordered feldspars (Smith and Parsons 1974; Sipling and Yund 1976; Parsons 1978). This has been ascribed to the fact, that Al–Si disordering increases the unit cell volume and facilitates mixing of the differently sized Na\(^+\) and K\(^+\) cations on the alkali cation site (Benisek et al. 2014; Hovis 2017), an effect that is qualitatively similar to the influence of increasing temperature. Based on solution calorimetry Hovis (2017) found a correlation between the maximum \(h^{ex}\) and the state of Al–Si ordering expressed as Z, with \(Z= X_{Al}^{T1o+T1m} - X_{Al}^{T2o+T2m}\) (Thompson 1969).
Such a correlation is missing in the feldspars investigated in our study. Interestingly, the \(W_{\text {g}\text {K}}\), \(W_{\text {g}\text {Na}}\) parameters calculated from the data of Hovis (2017) for the Al–Si ordering states of our feldspars are almost identical to those obtained from our partitioning experiments. According to literature data, the excess entropy \(s^\text {ex}\) of alkali feldspar solid-solution is independent of the Al–Si ordering state. Positive \(s^\text {ex,vib}\) has been reported for both ordered (Benisek et al. 2014) and disordered (Haselton et al. 1983) alkali feldspar solid-solutions (see Fig. 3b). In both studies, \(s^\text {ex,vib}\) was obtained from positive excess heat capacities measured by low-temperature calorimetry and additionally by differential scanning calorimetry (DSC) between 273 K and 773 K by Benisek et al. (2014). For pure end-members, heat capacities were determined with DSC between 350 K and 1000 K by Hemingway et al. (1981). In alkali feldspars, only Na- and K- vibrations, which are stimulated at low temperatures, contribute to \(s^\text {ex,vib}\). Therefore, \(s^\text {ex,vib}\) remains constant above about 200 K (Benisek et al. 2015). Also in plagioclase feldspars, \(s^\text {ex,vib}\) is more or less independent of T above 298 K, where, in contrast to alkali feldspars, high-frequency vibrations of tetrahedrons can play a role (Benisek et al. 2009). However, \(s^\text {ex,vib}\) obtained from low temperature calorimetry is applicable to the temperatures at which the experiments were performed (Benisek et al. 2015). The positive excess heat capacity and inferred excess vibrational entropy was ascribed to the increase of Na–O bond lengths and associated weakening of the bond with increasing \(X_\text {K}\), where the maximum effect is expected at intermediate compositions (Benisek et al. 2014, 2015). We determine positive \(s^\text {ex,vib}\) for V with maximum values of \(s^\text {ex,vib}\) of about 2 J\(\cdot\)mol\(^{-1}\cdot\)K\(^{-1}\) for intermediate compositions and with a similar, though less well constrained trend for M. For our data, comparison between \(s^\text {ex}\) and \(s^\text {ex,vib}\) yields negative \(s^\text {ex,con}\) at every composition (Fig. 3b) with a minimum at X\(_\text {K}\)=0.4. Negative excess entropy may be due to K–Na short range ordering, an inference that is corroborated by independent evidence for clustering of alkali cations in alkali feldspar (Phillips et al. 1988; Angel et al. 2013; Sanchez-Munoz et al. 2013).
All investigated feldspars slightly differ from pure binary solid-solutions due to incorporation of minor and trace elements (see Tables 1 and S2). For example, V, Z, and Zg have considerable celsian component with Ba present at concentrations of 0.013–0.016 a.p.f.u., and M has 0.044 a.p.f.u. Fe\(^{3+}\) on the tetrahedral site. None of these impurities seems to have a measurable effect on the Na–K partitioning between salt-melt and alkali feldspar, though. The fact that V and Zg, which have similar minor element composition but different Al–Si-ordering state, show similar Na–K partitioning renders it unlikely that the effects of minor elements and Al–Si ordering state cancel each other out. This is why we infer that neither variations of the Al–Si ordering state nor the variations in minor and trace element contents exhibited by the four feldspars used in our study and by the corresponding run products have a measurable influence on the Na–K partitioning between alkali feldspar and NaCl–KCl salt melt at temperatures between 800 \(^\circ\)C to 1000 \(^\circ\)C and at close to ambient pressure.
The solvus curves calculated for 1bar and for 1kbar based on our calibration of the Margules parameters and with the pressure effect for the 100 MPa solvus considered using the \(W_V\) parameters of Hovis et al. (1991) are shown in Fig. 5. Our solvus curves are compared with 100 MPa phase equilibrium data for disordered feldspars from Orville (1963); Luth and Tuttle (1966); Smith and Parsons (1974) and with 0.1 MPa phase equilibrium data for ordered feldspar from Bachinski and Müller (1971). The solvus curve obtained from our calibration is very similar to the ones given for disordered feldspars by Orville (1963); Luth and Tuttle (1966); Smith and Parsons (1974). The experimental data from Orville (1963); Smith and Parsons (1974) are very well reproduced by these solvus curves. Only the experimental data of Luth and Tuttle (1966) indicate a somewhat more asymmetric solvus with a steeper limb on the Na-rich side than the calculated solvus curves. There does not seem to be any systematic variation in the experimental data of Orville (1963); Luth and Tuttle (1966); Smith and Parsons (1974) that would allow to discern an effect of the Al–Si ordering state on the solvus, which is in line with our findings. Only the solvus curve given for ordered alkali feldspar of the low-albite - microcline series by Bachinski and Müller (1971) exhibits a substantially larger miscibility gap indicating the effect of highly ordered Al–Si. In contrast to the previous studies, which are based on phase equilibria at temperatures below the critical temperature of the solvus for disordered alkali-feldspar, our analysis is based exclusively on phase equilibria observed at temperatures above the critical temperature of the solvus for disordered alkali feldspar. The fact that extrapolation of \(g^\text {ex}\) and its temperature dependence obtained from Na–K partitioning at temperatures between 800 \(^\circ\)C and 1000 \(^\circ\)C reproduces phase equilibria that were experimentally determined at substantially lower temperatures suggests that the high-temperature partitioning experiments provide independent constraints on equilibrium phase relations in the alkali feldspar system even at lower temperatures, where attainment of equilibrium may be difficult in experiment.
Conclusions
The equilibrium partitioning of Na and K between alkali feldspar and NaCl–KCl salt melt was investigated experimentally at temperatures between 800 \(^\circ\)C and 1000 \(^\circ\)C and at a pressure of close to 0.1 MPa. Four different starting materials with Al–Si ordering states characterised by \(0.6 \le 2t_1 \le 0.9\), where \(2t_1\) is the T\(_1\) site fraction of Al\(^{3+}\), and slightly different minor and trace element compositions all yield similar partitioning curves indicating that neither the state of Al–Si ordering nor the minor and trace element concentrations have a measurable influence on Na–K partitioning over the range of Al–Si ordering states and minor element contents covered by the starting materials and the respective run products. From the thermodynamic analysis of the partitioning data the excess Gibbs energy accounting for the non-ideality of the alkali feldspar solid-solution including its temperature dependence were obtained. The corresponding solvus curve is slightly skewed to the Na rich side with a critical temperature of somewhat above 650 \(^\circ\)C at \(X_\text {K} = 0.39\), which is well comparable with literature data for low sanidine solvus. Comparison of excess vibrational entropy derived from heat capacity measurements by low-temperature calorimetry with the excess entropy obtained from the temperature dependence of the excess Gibbs energy yields negative configurational contributions to the excess entropy indicating clustering of Na and K on the alkali site. From the good agreement between the solvus curve obtained from Na–K partitioning experiments performed at temperatures well above the critical temperature of the solvus with two-feldspar phase equilibria determined by experiments performed at temperatures below the critical temperature of the solvus it is concluded that the high-temperature partitioning experiments provide valid and independent constraints on two feldspar equilibria.
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All relevant data is given in the supplementary information.
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Acknowledgements
This study was funded by the Austrian Science foundation, FWF Grant No. I 4404 to R. Abart and by FWF grant P33904 to E. Dachs. We gratefully acknowledge the thorough reviews by Guy Hovis and an anonymous reviewer, and we thank Jamie Connolly for fruitful discussions.
Funding
Open access funding provided by University of Vienna. This study was funded by the Austrian Science foundation, FWF Grant No. I 4404 and by FWF grant P33904 to E. Dachs.
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R.A. did the conceptualization of the project, D.H. carried out the experiments, E.P. contributed to the calculations, F.I. and E.D. performed the calorimetric measurements, C.L. did the pXRD analyses, C.H. did the ICP-MS analyses.
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Heuser, D., Petrishcheva, E., Ingegneri, F. et al. Thermodynamic mixing properties of disordered alkali feldspar solid-solution from Na–K partitioning and low-temperature calorimetry. Phys Chem Minerals 51, 9 (2024). https://doi.org/10.1007/s00269-024-01270-z
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DOI: https://doi.org/10.1007/s00269-024-01270-z