terclim by ICS banner
IVES 9 IVES Conference Series 9 Macrowine 9 Macrowine 2010 9 Impact of microbiological and enological techniques on wine macromolecules 9 The use of zirconia dioxide enclosed in a metallic cage for the stabilisation of Chardonnay white wine

The use of zirconia dioxide enclosed in a metallic cage for the stabilisation of Chardonnay white wine

Abstract

White wines are commonly stabilised by removing the heat unstable proteins through adsorption by bentonite, aneffective but inefficient wine processing step. Alternative absorbents are thus sought and zirconium dioxide (zirconia) is recognised as a promising candidate. The aim of this work was to assess the viability of zirconia treatments to stabilize white wines, with particular attention on process development. Effective protein removal was achieved by enclosing zirconia pellets into a metallic cage submerged in the wine. With this method the wine could be treated with the adsorbent for the time required for protein stabilisation, and then removed without further manipulation. Zirconia treatment of an unstable Chardonnay wine stabilised it without detectable modification of its physicochemical parameters and colour, apart from the removal of some metals (Cu, Fe) and acids. A simple, inexpensive and effective zirconia regeneration method was developed. Main drawbacks are the high dosages required and the necessity of stirring.

Publication date: July 3, 2024

Issue: Macrowine 2010

Type: Article

Authors

Matteo MARANGON1, Marco LUCCHETTA2, Elizabeth J. WATERS1

1 The Australian Wine Research Institute, P.O. Box 197, Glen Osmond (Adelaide), SA 5064, AUS.

2 Dipartimento di Biotecnologie agrarie, Centro Interdipartimentale per la Ricerca in Viticoltura ed Enologia (C.I.R.V.E.), Università di Padova, via dell’Università 16, 35020 Legnaro, PD, I.

Contact the author*

Keywords

Zirconium dioxide, protein stability, haze

Tags

IVES Conference Series | Macrowine | Macrowine 2010

Citation

Related articles…

Protein stabilization of white wines by stabilizing filtration: pilot studies

Protein stabilization is an important part of the winemaking process of white wines, and in this work we present the results of protein stabilization of different monovarietal wines (Xarel.lo, Chardonnay, and Muscat) by a continuous stabilizing filtration process using a column packed with zirconium oxide operating in a continuous regime in a closed loop at pilot scale.

Changes in wine secondary metabolites composition by the timing of inoculation with lactic acid bacteria: impact on wine aroma

For the first time, it was established that the timing of inoculation with LAB could significantly impact the concentration of many secondary metabolites leading to significant aromatic changes. From studied compounds, the most influenced were esters and diacetyl.

Polysaccharides and glycerol production by non-Saccharomyces wine yeasts in mixed fermentation

A great variability in the amount of polysaccharides recovered at the end of fermentations carried out by pure cultures of 89 non-Saccharomyces yeasts was observed. The utilization of the best polysaccharides producers in mixed cultures with S. cerevisiae resulted in considerable increases in the final concentration of polysaccharides and showed a strain dependent effect on glycerol production as compared to pure culture of S. cerevisiae.

Influence of dipping pretreatments in drying of ‘Pedro Ximenez’ grapes in chamber at controlled temperature

The influence of dipping pretreatments on drying of ‘Pedro Ximenez’ grapes, destined to the elaboration of sweet wines, in chamber at controlled temperature, has been studied. Changes in color and phenolic composition of raisins produced were observed during the process of raisining.

Identification and quantification of c-glucosidic ellagitannins and their derivative in red wine aged in oak barrels

The C-glycosidic ellagitannins constitute a subclass of hydrolyzable tannins of remarkable structural diversity. In this work we first achieved the hemisynthesis of flavano-ellagitannins, then we used them to develop a new efficient detection and quantification procedure for the C-glycosidic ellagitannins as well as flavano-ellagitannins.