Aluminum control on viscosity and structure of haplogranitic melts: Implications for rhyolitic melt viscosity determination

Accurate determination of melt viscosity near the glass transition temperature ( T g ) is critical for modeling volcanic processes, but direct measurements are often compromised by nanostructuration in natural Fe–Ti-bearing systems, especially during experimental manipulation. Differential scanning calorimetry (DSC) offers an alternative method for estimating viscosity via “shift factors” ( K ), which link enthalpy to shear relaxation (and thus shear viscosity). This is possible because DSC analysis of supercooled melts requires significantly less time than micropenetration viscometry. However, the compositional sensitivity of the shift factors is still debated, particularly in highly polymerized melts. To address this, we investigated the role of Al 2 O 3 in controlling melt viscosity and network structure using five Fe–Ti-free haplogranitic compositions: the metaluminous HPG8 base melt and four systematically modified variants with nominal composition of +2, +5, −2 and −5 wt% Al 2 O 3 . We combine micropenetration viscometry, DSC, and Raman spectroscopy to examine the rheological and structural response to Al 2 O 3 variation. Our results reveal a non-linear viscosity dependence on Al 2 O 3 content: peraluminous melts exhibit higher viscosities and T g , while peralkaline melts are significantly more fluid. Despite these differences, melt fragility remains constant across the compositional series. Calibrated DSC shift factors show no correlation with the network modifier content in peralkaline melts but instead they scale with the infinite-temperature viscosity (log 10 η ∞ ). Peralkaline melts with log 10 η ∞ > −3.00 show low and constant shift factors, whereas metaluminous and peraluminous melts (log 10 η ∞ < −3.00) yield higher values. These findings establish benchmarks for the application of the DSC shift-factor approach to estimate melt viscosity in natural, silica-rich rhyolitic melts, especially where direct measurements are hindered, thereby improving our ability to model magma rheology and eruption dynamics.

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Journal
Chemical Geology
Published
2025-11-04
DOI
https://doi.org/10.1016/j.chemgeo.2025.123127
Primary Topic
Geological and Geochemical Analysis
Type
article
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article

Aluminum control on viscosity and structure of haplogranitic melts: Implications for rhyolitic melt viscosity determination

Cláudia Romano, Danilo Di Genova, Donald B. Dingwell, Sumith Abeykoon et al.
Chemical Geology
Geological and Geochemical Analysis
article

Aluminum control on viscosity and structure of haplogranitic melts: Implications for rhyolitic melt viscosity determination

Cláudia Romano, Danilo Di Genova, Donald B. Dingwell, Sumith Abeykoon, Laura Calabrò, Veronica Stopponi, Dmitry Bondar, Gabriele F. Giuliani
article en

Abstract

Accurate determination of melt viscosity near the glass transition temperature ( T g ) is critical for modeling volcanic processes, but direct measurements are often compromised by nanostructuration in natural Fe–Ti-bearing systems, especially during experimental manipulation. Differential scanning calorimetry (DSC) offers an alternative method for estimating viscosity via “shift factors” ( K ), which link enthalpy to shear relaxation (and thus shear viscosity). This is possible because DSC analysis of supercooled melts requires significantly less time than micropenetration viscometry. However, the compositional sensitivity of the shift factors is still debated, particularly in highly polymerized melts. To address this, we investigated the role of Al 2 O 3 in controlling melt viscosity and network structure using five Fe–Ti-free haplogranitic compositions: the metaluminous HPG8 base melt and four systematically modified variants with nominal composition of +2, +5, −2 and −5 wt% Al 2 O 3 . We combine micropenetration viscometry, DSC, and Raman spectroscopy to examine the rheological and structural response to Al 2 O 3 variation. Our results reveal a non-linear viscosity dependence on Al 2 O 3 content: peraluminous melts exhibit higher viscosities and T g , while peralkaline melts are significantly more fluid. Despite these differences, melt fragility remains constant across the compositional series. Calibrated DSC shift factors show no correlation with the network modifier content in peralkaline melts but instead they scale with the infinite-temperature viscosity (log 10 η ∞ ). Peralkaline melts with log 10 η ∞ > −3.00 show low and constant shift factors, whereas metaluminous and peraluminous melts (log 10 η ∞ < −3.00) yield higher values. These findings establish benchmarks for the application of the DSC shift-factor approach to estimate melt viscosity in natural, silica-rich rhyolitic melts, especially where direct measurements are hindered, thereby improving our ability to model magma rheology and eruption dynamics.

Chemical GeologyVol. 698
Università di Camerino (IT), Roma Tre University (IT), Institute of Science and Technology for Ceramics (IT), National Research Council (IT), University of Bayreuth (DE), Ludwig-Maximilians-Universität München (DE), Beihang University (CN)
Openalex Percentile: Top 66%
Geological and Geochemical Analysis
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