Open access peer-reviewed chapter

Air Depleted and Solvent Impregnated Cork Powder as a New Natural and Sustainable Wine Fining Agent

Written By

Luís Filipe da Mota Ribeiro, Maria Fernanda Gil Cosme Martins and Fernando Hermínio Ferreira Milheiro Nunes

Reviewed: 07 March 2019 Published: 23 May 2019

DOI: 10.5772/intechopen.85691

From the Edited Volume

Advances in Grape and Wine Biotechnology

Edited by Antonio Morata and Iris Loira

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Abstract

We recently proposed a simple methodology to improve cork powder waste adsorption properties through vacuum degassing and solvent impregnation, to use this abundant and cheap material as a new wine fining agent. Its applicability was first shown for red wine 4-ethylphenol (4-EP) and 4-ethylguaiacol (4-EG) reduction. Nowadays, the presence of 4-EP and 4-EG is a serious problem in the wine industry, known as “Brett character”, by the negative aroma imparted by these volatile phenols (VPs) to red wine. There are only some curative treatments to remove these compounds without impacting negatively on wine quality. Optimised cork powder was used successfully as a new treatment for the reduction of these negative VPs (41?75% for 4-EP and 40?69% for 4-EG) increasing at the same time wine sensory performance. Wine treated with cork powder reduced 6.9% phenolic acids and catechin and 2.3% monomeric anthocyanins without any significant change in colour intensity. In this chapter, the cork complex structure is discussed, besides the impact of its use in wine containing VPs on physicochemical composition and quality. This new application of this natural, abundant and cheap material has the potential of being a new wine fining agent with low environmental impact.

Keywords

  • cork composition
  • adsorption properties
  • red wine
  • volatile phenols
  • aroma
  • phenolic compounds
  • sensory attributes

1. Introduction

Cork, the outside part of the oak (Quercus suber L.), is a natural, renewable, sustainable raw material, which is periodically harvested from the tree, usually every 912 years, depending on the cultivation region [1]. Quercus suber L. is a tree that grows slowly in same regions of the western Mediterranean (Portugal, Spain, Southern France, part of Italy and North Africa) and China [2, 3, 4]. Portugal is the main cork producer, transforming about 75% of all the cork [3, 4]. Industrial transformation of cork generates up to 25 wt.% of cork dusts as by-product [5, 6].

Cork wastes and cork powders have been used as bioadsorbents for removing pesticides and other pollutants from wastewaters with promising results [7]. Biosorption is an emergent technology expected to show strong growth soon because it offers high cost effectiveness, although further improvements in its performance are needed [1]. Environmental protection legislation is becoming progressively important and effective solutions will be at premium [8].

The cork material is compact, devoid of intercellular spaces and with a regular honeycomb organisation (Figure 1). This material is composed by dead parenchymatous cells with voids, prismatic, air-filled interiors, hexagonal on average and are arranged base-to-base in an alignment oriented in the tree’s radial direction [9].

Figure 1.

Structure of cork as observed by SEM in the two main sections: (A) tangential section, perpendicular to the tree’s radial direction; (B) transverse section, perpendicular to the tree’s axial direction.

The cells are small and have sizes under those of synthetic foams. The area of the prism base is 46 × 10−6 cm with a mean prism edge of 1315 μm; prim height is usually in the range of 3040 μm. The mean cell volume is approximately 2 × 10−8 cm3 and the number of cells per unit is 47 × 107 cm−3. The cell walls are thin with a thickness of 11.5 μm. The solid mass volume fraction of the cork is only about 10%.

Cork powder maintains the cork cellular structure intact [10], and its adsorption properties can be improved by removing the air and simultaneous impregnation with ethanol rendering the cell wall components more accessible to the adsorbates [10]. This simple treatment was shown to increase cork powder adsorption capacity of 4-EP and 4-EG by at least 4 times in a real wine matrix, with the cork powder adsorption capacity increasing with the increase in concentration of these wine contaminants [10].

In red winemaking, especially those aged in wood barrels, the contamination and growth of Dekkera/Brettanomyces yeasts result in the formation of 4-EP and 4-EG by decarboxylation of p-coumaric and ferulic acids present in wine and subsequent reduction of the correspondent vinylphenols (Figure 2) [11, 12].

Figure 2.

Formation of volatile phenols from hydroxycinnamate precursors or their degradation products (vinylphenols) in wines by Dekkera/Brettanomyces.

These VPs are responsible for negative aromatic notes like horsy sweat, smoky, barnyard and medicinal [11, 13]. This important sensory defect has been reported in several wine styles around the world, especially, premium wines [14, 15], considered negative by professionals, consumers and wine industry [16, 17], and thus, VPs are a generalised problem in red winemaking.

For these reasons, several treatments to avoid or to reduce compounds have been tested. Preventive action includes, for example, the maintenance of adequate levels of sulphur dioxide throughout the winemaking process, reduction/elimination of oxygen levels in wine, use of dimethyl dicarbonate (DMDC) before bottling and the addition of fungal chitosan, which are some of the measures that have found some degree of success [18, 19]. Several remediation treatments have also been developed to eliminate the already formed VPs from wine or to decrease the headspace content by decreasing their partition coefficients to the gas phase without changing the total wine VP content. Of these methods, those tested in wines presenting good removal efficiency at practical application doses are activated carbons [20, 21], potassium caseinate [22], egg albumin [22] and esterified cellulose [23]. Nevertheless, although they are efficient in reducing the total amount of VPs in wines, the use of potassium caseinate and egg albumin presented the risk of the potential allergenicity of these fining agents and therefore it is mandatory to label the wine bottle if the residual concentration is higher than 0.25 mg/L (EU Regulation 579/2012). For the decrease of headspace abundance of VPs chitosans has been shown to be effective [24].

The success of cork powder in adsorption of VPs from such a complex matrix as wine without affecting the wine quality significantly in terms of phenolic composition is certainly due to the structure and chemical composition of its main components namely suberin, lignin and cell wall polysaccharides.

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2. Cork chemical composition

The chemical composition of cork has been widely examined [25, 26, 27, 28, 29, 30, 31, 32, 33] and presented some variability that depends on factors such as geographic origin, soil and climate conditions, genetic origin, tree dimensions, age and growth conditions (Table 1). Cork from Quercus suber L. has specific properties such as low permeability and great elasticity; this is the result, at least partially, from its specific chemical composition (and more especially from that of suberin) [26, 29, 31, 32, 33]. The cork cell wall structure consists in a thin internal primary cork cell wall rich in lignin and a thick secondary wall rich in suberin, alternating with a wax lamella and a thin tertiary wall of polysaccharides.

Principal components (%) Range Average
Suberin 40–53 45.8
Lignin 21–29 24.4
Polysaccharides 10–16 12.5
Extractives 6–19 12.6
Tannins 6–7 6.5
Ash 0.85–2.1 1.4

Table 1.

Chemical composition of cork.

Adapted from [1, 25, 34, 35, 36].

2.1 Suberin

Suberin, a natural aliphatic-aromatic crosslinked polyester, is the major component of cork, accounting for 30–50% of its weight. It is a very important structural component of the cell wall and its removal destroys cell integrity. Suberin polymeric structure is mainly composed by two types of monomers, glycerol and long-chain fatty acids and alcohols, which are linked by ester bonds, Figure 3 [9].

Figure 3.

Schematic representation of suberin structure (adapted from Graça [37]).

2.2 Lignin

Lignin is the second most important component in cork cell walls accounting for 15–30% of its weight [9]. It is a crosslinked polymer of aromatic nature. Due to the importance of lignin, many studies were done in wood pulping and more recently, for biomass deconstruction [38]. Lignin is a polymer made up by three monomer types of phenyl propane (p-coumaryl, coniferyl and sinapyl alcohols) linked through a free-radical reaction started via enzymatic phenoxy radical formation (Figure 4). The inter-unit linkages in the polymer can be of several kinds: β-O-4′, α-O-4′, β-β´, β-5′, 5-5′, 4-O-5′ or β-1′. The specific relation of the monomers and intermonomeric linkages depend on the material [9]. In cork, lignin also contributes to the mechanical support and rigidity of the cell walls. If lignin is selectively removed from cell walls, a total collapse of the cells is observed.

Figure 4.

Schematic representation of lignin structure (adapted from Achyuthan et al. [39]).

2.3 Polysaccharides

In cork, the cell wall polysaccharides, cellulose and hemicelluloses, represent approximately 20% of its weight. Cellulose is in the primary and tertiary cell walls of cork, accounting for nearly 10% [40]. There is less information concerning the molecular weight, crystallinity and chain orientation of cork cellulose. Cellulose is water insoluble due to an extensive intermolecular hydrogen bonding between adjacent polymers, and interaction with water often only occurs in the amorphous regions. The hemicelluloses are another water insoluble group of polysaccharides present in cork cell walls. The main known hemicellulose polysaccharides comprise three different groups of polysaccharides (Figure 5), the 4-O-methylglucuronoxylan, arabino-4-O-methylglucuronoxylan and 4-O-methylglucurono-arabinogalactoglucoxylan [41, 42, 43, 44]. Xylans in the cell walls are amorphous and the irregular occurrence of branching of the main chain does not permit strong intermolecular association by hydrogen bonding; nevertheless, they are extracted using strong alkaline solutions (4–10% w/v NaOH). Pectins also exist in low quantities in cork, approximately 1.5%, placed in the middle lamella [45].

Figure 5.

Schematic structures of main cork cell wall polysaccharides: (a) cellulose, (b) 4-O-methylglucuronoxylan, (c) arabino-4-O-methylglucuronoxylan and (d) 4-O-methylglucurono-arabinogalactoglucoxylan.

2.4 Extractable components

Cork contains 8–20% of low molecular weight compounds including fatty acids, terpenes, long-chain aliphatic compounds and saccharides, collectively known as extractives [34, 46]. Cork contains also about 6% of tannins [36]. The most important of these components are waxes and tannins [31]. Waxes are extracted by low polarity solvents, such as benzene, chloroform, ethyl acetate [47], hexane [36] and ether [26]. The waxes are responsible for the cork impermeability. The waxes extracted were found to consist of two fractions: neutral and acidic. The neutral fraction is mostly composed of fatty alcohols (C18▬C26) with some unsaturated groups and triterpenes.

The acid fraction is essentially composed of fatty acids (C14▬C24) with unsaturated ω-hydroxyacids, 18-hydroxy-9,12-octadienoic and 18-hydroxy-9-octadecenoic acids. More or less 50% of the waxes are triterpenes from friedelin and lupine families including friedelin, 3-α-hydroxyfriedelan-2-one, botulin, betulinic acid, β-sitosterol and sitost-4-en-3-one [48]. Cork extractable phenolic compounds include ellagic acid and some quantities of gallic acid, protocatechuic acid/aldehyde, aesculetin, vanillic acid, caffeic acid, vanillin, scopoletin, ferulic acid, coniferyl aldehyde and sinapaldehyde [49, 50]. The extraction of tannins can be done by polar solvents such as water [51] and ethanol [52]. Cork tannins include roburins A and E, grandini, vescalagin and castalagin. The yields of these two components change in function of the nature of the cork (virgin or reproduction) where significant variation is found in the bibliography [1].

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3. Optimised cork powder (CKP) as a wine fining agent to remove negative volatile phenols in contaminated red wine

The air removal of the cork powder cell structure and simultaneous impregnation with ethanol with or without previous removal of cork extractives increased significantly the 4-ethylphenol and 4-ethylguaiacol adsorption performance (Table 2).

Although a significant removal of wine VPs was observed, the overall quality of the treated wine cannot be accessed only by the decrease in these negative aroma compounds, as the impact on the other wine positive aroma components is important to define the final overall sensory olfactory quality [15, 20, 21, 22, 24]. The red wine colour characteristics are important for consumer acceptance of the treated wine, because there is straight relation between the colour and the wine’s phenolic composition, namely anthocyanins, whose concentration can be changed by the fining procedure.

In order to have a deeper insight on the impact of optimised cork powder in the wine chemical composition besides the removal efficiency of the VPs, the change in the headspace aroma abundance of wine, phenolic composition and chromatic characteristics were studied and the overall impact on the wine sensory characteristics was evaluated by an expert panel.

3.1 Impact of optimised cork powder on the wine aroma headspace abundance

Air removal and ethanol impregnation of cork samples with and without extractive removal decreased the total headspace aroma abundance (CKNI 32% and CKFI 37%) significantly. The decrease in the particle size of the CKF did not differ significantly on the removal of headspace aroma compounds, although there was an average decrease of 3.7% in relation to CKF (Table 3). The duplication in application dose of CKFI75 resulted in a significant decrease of the total abundance of headspace aroma by more 29% (Table 3). There was a significant correlation (r = 0.731, n = 14, p < 0.003) between the headspace aroma abundance and the octanol-water partition coefficient (log P) of the aroma compounds, strongly suggesting that the interaction of the volatile compounds including the VPs with the cork powder is of hydrophobic nature as observed for the interaction of other molecules with cork [7, 53, 54]. When compared to activated carbons applied at 100 g/hL, CKFI75250 (250 g/hL) showed a lower impact on the headspace aroma abundance (40 vs. 75%) and even CKFI75500 (500 g/hL) resulted in a lower reduction of 69%. Therefore, cork powder decreased the wine headspace aroma compounds lesser than the activated carbons [21].

Factors Wine spiked levels
Medium High
A B 4-EP 4-EG 4-EP 4-EG
No impregnation CKN 85.3 ± 2.7a 9.2 ± 0.2a 109.6 ± 5.1a 10.5 ± 0.6a
CKF 168.8 ± 4.2b 19.2 ± 2.7b 738 ± 36.9b 71.5 ± 5.4b
Vacuum impregnation CKNI 270.9 ± 11.8c 43.4 ± 2.1c 888.0 ± 16.3c 133.8 ± 2.0c
CKFI 306.0 ± 2.3d 60.5 ± 1.6d 1036.5 ± 18.1d 149.1 ± 3.3d
A 0.0000001 0.000011 0.0000001 0.0000001
B 0.0000001 0.0000001 0.0000001 0.0000001
A × B 0.0029 0.083033 0.0000001 0.000018

Table 2.

Amount of 4-EP and 4-EG (μg/L) removed from wines at two spiked levelsa of natural cork powder (CKN) and dichloromethane and ethanol extractive free cork powder (CKF) before and after air removal and impregnation with ethanol (CKNI and CKNFI) [10].

Values are presented as mean ± standard deviation; medium spiking levels: 750 μg/L 4-EP and 150 μg/L 4-EG; high 1500 μg/L 4-EP and 300 μg/L 4-EG. Means within a column followed by the same letter are not significantly different ANOVA and Tukey post-hoc test (p < 0.05).


Compounds ID RI calculated RI Odour descriptor ODT (mg/L) T0 TF CKNI CKFI CKFI75250 CKFI75500
Ethyl acetate 725 715 Fruity 7.5 23.97 ± 1.67a 23.29 ± 2.97a 14.32 ± 0.88b 14.13 ± 0.42b 14.70 ± 1.84b 8.53 ± 1.49c
3-Methylbutan-1-ol-acetate std 1121 1126 Banana 0.03 65.09 ± 15.64a 67.59 ± 19.86a 44.36 ± 3.22a 39.81 ± 4.81ab 35.30 ± 3.50ab 16.93 ± 3.95b
2-Methyl-1-butanol std 1229 1223 Malty 0.48 112.02 ± 8.60a 109.52 ± 8.6a 77.47 ± 2.20c 71.24 ± 3.46c 76.13 ± 5.49c 50.10 ± 8.03d
Ethyl hexanoate std 1229 1262 Green apple 0.014 27.62 ± 16.17a 27.87 ± 15.68a 25.65 ± 0.67ab 22.45 ± 1.30ab 20.69 ± 4.13b 12.92 ± 2.43b
Ethyl octanoate std 1441 1429 Fruity 0.005 164.67 ± 19.71a 167.17 ± 10.85a 104.94 ± 6.78b 90.56 ± 12.53b 75.94 ± 27.94b 43.14 ± 1.49c
Ethyl decanoate std 1648 1646 Fruity 1.5 78.55 ± 3.63a 78.95 ± 5.89a 67.12 ± 6.21ab 53.94 ± 7.51b 36.93 ± 23.29c 19.61 ± 2.20c
Diethyl succinate std 1683 1698 Light fruity 7.5 66.90 ± 1.14a 64.40 ± 3.94a 41.95 ± 1.74cd 41.22 ± 1.81d 39.72 ± 3.78d 23.56 ± 5.20e
Phenylethyl acetate std 1809 1833 Flowery 0.25 31.16 ± 4.66a 30.16 ± 3.51a 22.82 ± 0.89b 20.54 ± 1.13b 14.80 ± 6.94c 8.49 ± 2.96c
2-Phenylethanol std 2000 1911 Roses 14.0 365.23 ± 19.85a 362.73 ± 31.57a 247.32 ± 7.78b 240.73 ± 15.31a 216.92 ± 39.38b 136.16 ± 60.27c
4-Ethylguaiacol std 2012 1989 Smoke 0.15 n.d. 16.62 ± 0.89a 9.21 ± 0.41c 9.05 ± 0.68c 8.00 ± 2.25c 3.70 ± 1.07d
Reduction SPME (%) 44.6 45.6 50.6 77.8
Octanoic acid std 2036 2030 Rancid 0.5 17.87 ± 0.57a 17.62 ± 0.73a 6.00 ± 3.79cd 8.98 ± 0.97bc 7.19 ± 1.32cd 2.30 ± 1.20d
4-Ethylphenol std 2084 2142 Phenolic 0.4 n.d. 18.25 ± 1.23a 10.37 ± 0.31c 9.83 ± 0.89c 7.94 ± 2.19c 3.37 ± 1.35d
Reduction SPME (%) 43.1 46.1 56.5 81.5
Decanoic std 2129 2196 Rancid 1.0 4.14 ± 0.45a 4.19 ± 0.43a 1.49 ± 0.17ab 2.53 ± 2.76ab 1.24 ± 0.62ab n.d
Dodecanoic std 2136 2156 Waxy 6.1 5.48 ± 0.36a 5.23 ± 0.59a 0.93 ± 0.15c 0.90 ± 0.41c 0.90 ± 0.13c n.d
Total area-VPs 962.7 ± 28.0a 958.7 ± 46.7a 652.9 ± 10.1cd 607.0 ± 32.1d 571.1 ± 68.3d 296.7 ± 71.1e
Reduction (%) 31.9 36.7 40.4 69.1

Table 3.

Headspace aroma profile of red wines before (VP-free T0 and VP-spiked with 750 μg/L of 4-EP and 150 μg/L of 4-EG, TF) and after treatment with natural cork and dichloromethane and ethanol extractive free cork after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL) (CKF75250 and CKFI75500).

Results are expressed in absolute area (×105). Data are presented as X ¯ ± s ; ID, identification; std, standard; and RI, retention index [60, 61, 62], MW, molecular weight; LOD, limit of olfactory detection). Odour descriptor [63, 64, 65]. Values within a line followed by the same letter are not significantly different ANOVA and Tukey post-hoc test (p ˂ 0.05). n.d., not detected; uncontaminated (T0) spiked red wine (TF) and wines treated with corks.p < 0.05.

3.2 Impact of optimised cork powder on wine chromatic characteristics and phenolic compounds

Application of optimised cork powder results in a decrease of the colour intensity, although being only significantly different from the control for the CKFI and CKFI75500. For the L* and a*, the same was observed (Table 4). These variations for the colour intensity are not due to a decrease in the concentration of monomeric anthocyanins that generally did not change by the use of all cork powders (Table 5). For the individual phenolic acids overall, their levels did not change significantly, or their decrease was significant but small, and these decreases occurred mainly for the CKFI75 at the two application doses (decreased for trans-caftaric acid—5.6%; coutaric acid—5.9%; caffeic acid—20%; ferulic acid—12% and coumaric acid ethyl ester—19%) (Table 5). For catechin, there was no change in its levels for all cork powders applied. These results show that optimised cork powders, either with or without extractive removal, have a low impact on wine phenolic composition; nevertheless, the ethanol impregnated extractive free corks had a significant impact on wine colour intensity, suggesting that these corks influence wine polymeric pigments as no significant changes on monomeric anthocyanins were observed. The impact for cork powders on wine phenolic composition and colour intensity of wines was lower than that generally observed for activated carbons used at 100 g/hL [20].

Samples L* a* b* C* ΔE Colour intensity (A.U.) Hue
T 10.84 ± 0.49a 40.55 ± 0.68a 35.62 ± 0.31ab 53.97 ± 0.72ab 0.72 ± 0.00a 10.04 ± 1.04a 0.66 ± 0.00a
CKNI 13.17 ± 0.18b 43.32 ± 0.23b 35.47 ± 0.00ab 55.99 ± 0.18b 0.69 ± 0.00c 3.54 ± 0.29ab 9.09 ± 0.07ab 0.72 ± 0.00b
CKFI 13.87 ± 0.08c 44.37 ± 0.01b 36.22 ± 0.29b 57.28 ± 0.19b 0.68 ± 0.00c 4.88 ± 0.01b 8.97 ± 0.17b 0.71 ± 0.01b
CKFI75250 10.85 ± 0.72a 40.72 ± 1.14a 34.08 ± 0.99ab 53.10 ± 1.51ab 0.70 ± 0.00b 1.99 ± 0.48a 9.40 ± 0.07ab 0.74 ± 0.00c
CKFI75500 14.84 ± 0.20c 45.32 ± 0.34b 36.17 ± 0.27b 57.98 ± 0.44b 0.67 ± 0.00c 6.35 ± 0.41b 8.34 ± 0.01b 0.76 ± 0.01c

Table 4.

Chromatic characteristics of red wines before (TF) and after treatment with natural cork and dichloromethane and ethanol extractive free cork after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL).

Data are presented as X ¯ ± s ; data within a column followed by the same letter are not significantly different (Tukey, p ˂ 0.05). L*, lightness; a*, redness; b*, yellowness; ΔE*, colour difference. The values corresponding to ΔE* were obtained taking as a reference the untreated wine (T) and wines treated with corks (CKNI, CKFI, CKFI75250 and CKFI75500). A.U., absorbance units.p < 0.05.

Samples Del-3-Glc Cya-3-Glc Pet-3-Glc Peo-3-Glc Mal-3-Glc Del-3-AcGlc Cya-3-AcGlc Mal-3-AcGlc Del-3-CoGlc Cya-3-CoGlc Mal-3-CoGlc
T 1.18 ± 0.00 8.24 ± 0.17a 13.58 ± 0.30a 4.77 ± 0.07a 155.84 ± 0.69a 1.58 ± 0.02a 0.98 ± 0.00a 26.04 ± 0.46a 1.37 ± 0.02a 1.49 ± 0.15a 13.70 ± 0.78a
CKNI 1.12 ± 0.02 7.66 ± 0.12b 13.10 ± 0.06a 4.55 ± 0.04b 150.37 ± 1.21b 1.24 ± 0.01d 0.79 ± 0.03b 25.66 ± 0.30a 1.24 ± 0.02a 1.43 ± 0.04a 12.09 ± 0.53ab
CKFI 1.14 ± 0.03 8.00 ± 0.05ab 13.59 ± 0.03 4.78 ± 0.03a 156.65 ± 1.05a 1.50 ± 0.00b 0.87 ± 0.01ab 26.69 ± 0.35a 1.31 ± 0.02b 1.23 ± 0.04a 12.61 ± 0.14ab
CKFI75250 1.15 ± 0.02 7.71 ± 0.19ab 13.66 ± 1.15 4.53 ± 0.01b 154.04 ± 0.36ab 1.42 ± 0.04c 0.83 ± 0.04ab 25.89 ± 0.91a 1.29 ± 0.05a 1.08 ± 0.28a 11.89 ± 0.48b
CKFI75500 1.12 ± 0.01 7.93 ± 0.06ab 13.42 ± 0.23 4.67 ± 0.08ab 154.08 ± 2.30ab 1.34 ± 0.02c 0.84 ± 0.05ab 26.68 ± 0.56a 1.30 ± 0.04a 1.18 ± 0.01a 12.04 ± 0.32ab
Gallic acid Catechin t-Caftaric acid Coutaric acid Caffeic acid p-Coumaric acid Ferulic acid Caffeic acid ethyl ester Coumaric acid ethyl ester
T 24.11 ± 1.55a 9.28 ± 1.53a 30.02 ± 0.25a 11.23 ± 0.18ab 0.84 ± 0.00a 0.72 ± 0.01a 0.57 ± 0.00a 0.39 ± 0.00a 3.89 ± 0.04a
CKNI 21.92 ± 1.79a 8.55 ± 1.16a 29.61 ± 0.28a 11.02 ± 0.20ab 0.80 ± 0.08a 0.57 ± 0.03b 0.54 ± 0.00b 0.33 ± 0.04ab 3.37 ± 0.18b
CKFI 22.50 ± 0.30a 8.48 ± 1.10a 29.23 ± 0.02ab 10.81 ± 0.01ab 0.69 ± 0.01b 0.55 ± 0.00b 0.52 ± 0.01c 0.33 ± 0.00ab 3.28 ± 0.03b
CKFI75250 22.77 ± 0.07a 8.27 ± 0.26a 28.57 ± 0.44b 10.56 ± 0.29b 0.67 ± 0.03b 0.68 ± 0.02a 0.50 ± 0.01c 0.31 ± 0.02ab 3.15 ± 0.15b
CKFI75500 25.02 ± 0.09a 7.74 ± 0.61a 28.09 ± 0.56b 10.57 ± 0.18b 0.66 ± 0.00b 0.67 ± 0.01a 0.50 ± 0.01c 0.31 ± 0.01b 3.12 ± 0.02b

Table 5.

Monomeric anthocyanin and phenolic acid composition of spiked red wines (TF) and after treatment with natural cork and dichloromethane and ethanol extractive free cork after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL) (CKFI75250 and CKFI75500).

Values are presented as X ¯ ± s ; means within a column followed by the same letter are not significantly different (Tukey, p ˂ 0.05). Del-3-Glc, delphinidin-3-glucoside, Cya-3-Glc, cyanidin-3-glucoside, Pet-3-Glc, petunidin-3-glucoside, Peo-3-Glc, peonidin-3-glucoside, Mal-3-Glc, malvidin-3-glucoside, Del-3-AcGlc, delphinidin-3-acetylglucoside, Cya-3-AcGlc, cyanidin-3-acetylglucoside, Pet-3-AcGlc, petunidin-3-acetylglucoside, Peo-3-AcGlc, peonidin-3-acetylglucoside, Mal-3-AcGlc, malvidin-3-acetylglucoside, Del-3-CoGlc, delphidin-3-coumaroylglucoside, Cya-3-CoGlc, cyanidin-3-coumaroylglucoside, Pet-3-CoGlc, petunidin-3-coumaroylglucoside, Peo-3-CoGlc, peonidin-3-coumaroylglucoside and Mal-3-CoGlc, malvidin-3-coumaroylglucoside. Data within a column followed by the same letter are not significantly different ANOVA and Tukey post-hoc test (p < 0.05).p < 0.05.

3.3 Impact of optimised cork powder on wine sensory attributes

To validate the impact of natural and extractive free ethanol impregnated cork powder samples on the headspace VP decrease and its effect on the sensory perception and quality of wines, CKNI, CKFI and CKFI75—treated wines at the two application doses (250 and 500 g/hL, CKFI75250 and CKFI75500, respectively) were subjected to sensory analysis by an expert panel. As expected, the presence of these VPs affect the aroma profile of spiked wine (TF) significantly and negatively (Table 6), by the increase of the phenolic attribute, decreasing the wine fruity and floral attributes significantly [20, 24, 55]. The panel consensus on each wine attribute was accessed through the percentage of variance explained by the first PCA [56] applied to the panel scores for each attribute. The variance explained by PC1 ranged from 45 to 87%, yielding the C-indexes presented in Table 6. Similar values have been reported for trained panels assessing different attributes and different products [20, 24, 62]. Colour intensity, floral, fruity, phenolic, acidity, balance and persistence wine attributes resulted in a consensus among judges (Table 6). For the colour hue, limpidity, oxidised (visual), vegetable, oxidised (aroma) and body, the judges attributed identical scores. There is no consensus on the other sensory wine attributes that could be due to the low difference of the attributes among samples or changes in motivation, sensitivity and psychological answer behaviour [57].

T0 TF CKNI CKFI CKFI75250 CKFI75500 p C-index1
Intensity 3.70 ± 0.48a 3.70 ± 0.48a 3.60 ± 0.52ab 3.40 ± 0.52b 3.40 ± 0.52b 2.70 ± 0.48c p < 0.000001 3.3
Hue 3.40 ± 0.52a 3.40 ± 0.52a 3.40 ± 0.52a 3.30 ± 0.48a 3.40 ± 0.52a 3.00 ± 0.67b p < 0.000001
Limpidity 3.40 ± 0.84 3.40 ± 0.84 3.40 ± 0.84 3.40 ± 0.84 3.40 ± 0.84 3.40 ± 0.84 p = 1.0
Oxidised (visual) 1.80 ± 0.42 1.80 ± 0.42 1.80 ± 0.42 1.80 ± 0.42 1.80 ± 0.42 2.00 ± 0.00 p < 0.811
Fruity 3.60 ± 0.52a 1.70 ± 0.48b 2.20 ± 1.14c 2.20 ± 0.79c 2.60 ± 1.07d 2.20 ± 1.23c p < 0.000001 1.6
Floral 2.50 ± 0.53a 1.30 ± 0.65b 1.40 ± 0.52b 1.60 ± 0.84c 1.80 ± 1.03d 1.40 ± 0.52b p < 0.000001 2.5
Vegetable 1.40 ± 0.52a 1.80 ± 0.42b 1.80 ± 0.42b 1.70 ± 0.48b 1.70 ± 0.48b 1.80 ± 0.42b p < 0.00016
Phenolic 1.10 ± 0.32a 3.80 ± 0.63b 2.70 ± 0.48c 2.70 ± 0.48c 2.80 ± 0.42c 2.80 ± 0.42c p < 0.000001 6.3
Oxidised (aroma) 2.00 ± 0.67a 2.60 ± 0.52b 2.40 ± 0.84ab 2.80 ± 0.42b 2.40 ± 0.84ab 2.80 ± 0.42b p < 0.066
Bitterness 1.70 ± 0.67a 2.30 ± 0.48b 2.20 ± 0.42b 2.20 ± 0.42b 2.20 ± 0.42b 2.00 ± 0.67a p < 0.0307 0.9
Acidity 2.20 ± 0.79 2.70 ± 0.48 2.60 ± 0.52 2.60 ± 0.52 2.60 ± 0.52 2.30 ± 0.48 p < 0.0605 1.1
Astringency 2.00 ± 0.67a 2.60 ± 0.52b 2.80 ± 0.42c 2.40 ± 0.52d 2.40 ± 0.52d 2.50 ± 0.85bd p < 0.000001 0.8
Body 2.70 ± 0.48 2.50 ± 0.53 2.40 ± 0.52 2.50 ± 0.53 2.40 ± 0.84 2.50 ± 0.53 p < 0.333
Balance 3.00 ± 0.67a 2.20 ± 0.42b 2.0 ± 0.67b 2.40 ± 0.52b 2.40 ± 0.52b 2.20 ± 0.42b p < 0.0037 1.1
Persistence 3.00 ± 0.67a 2.00 ± 0.67b 2.20 ± 0.42c 2.40 ± 0.52d 2.40 ± 0.52d 2.40 ± 0.52d p < 0.000001 3.1

Table 6.

Mean scores of each attribute after sensory analysis of volatile phenol-free (T0) and volatile phenol-spiked (TF) red wine after treatment with natural cork and dichloromethane and ethanol extractive free cork after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL) (CKFI75250 and CKFI75500).

Consonance analysis results—no variance observed for most panellists. Data are presented as the X ¯ ± s (n = 12); data within a line followed by the same letter are not significantly different (Duncan p < 0.05).p < 0.05.


In accordance with the instrumental colour intensity, sensory colour intensity of the wines treated with ethanol impregnated extractive free cork powders was significantly lower than T0 and TF, with the increase in the application dose (CKFI75500) presenting a significantly lower score than CKFI75250 and CKFI. This decrease in colour intensity in the CKFI75500 is also followed by a decrease in the sensory hue, being in accordance with the significant change in h° and L* for this sample. Neither natural nor extractive free cork powders changed significantly the limpidity and oxidised visual sensory attributes.

For VP-spiked wine, the application of all cork powders in two application doses (250 and 500 g/hL) of CKFI75 decreased the negative phenolic attribute significantly compared to the spiked wine (TF); however, the scores obtained were also significantly higher than those observed for the initial unspiked wine (T0). For the fruity aroma attribute, the application of all cork powder allowed recovering significantly the fruity aroma attribute in relation to the VP-spiked wine (TF); nevertheless, the scores were also significantly lower than that observed for the original unspiked wine (T0). The fruity aroma attribute was significantly higher for the CKFI75250 than for all other cork powder samples even higher than CKFI75500. This could be due to the higher decrease in headspace aroma abundance responsible for the fruity notes for this application dose as discussed previously.

For the floral attribute, only CKFI and CKFI75250 allowed increasing significantly this sensory attribute in relation to the TF, and again the scores obtained for the cork-treated wines were significantly lower than that obtained for T0. As observed for the fruity attribute, also for the floral attribute the increase in application dose of CKFI75 decreased the floral attribute of the wine (Table 6). The TF wine presented an increased vegetable attribute that did not decreased with the application of cork powder samples, nevertheless, the scores observed was very low (Table 6). No significant differences were observed for the oxidised aroma attribute in all samples (T0, TF and cork powder treated wines).

The application of cork powder did not change the acidity and body of the wine samples significantly; however, significant differences were obtained for bitterness, astringency, balance and persistence (Table 6). The spiking wine resulted in a significant increase in the bitterness attribute in relation to the T0. Except for CKFI75500, the other cork powders did not decrease bitterness to the levels observed for T0. For astringency, spiking of wine with VPs increase this sensory attribute, and no cork-powder sample decreased the astringency to the initial levels (T0), nevertheless CKFI and CKFI75250 were able to decrease significantly the astringency in relation to TF. For CKNI, a significant increase of astringency in relation to TF was observed, and this can be explained probably by a migration of phenolic compounds from this cork-powder [58, 59]. For balance, TF significantly decreased this sensory attribute, and the application of all cork powders did not lead to scores significantly different from the TF. For persistence, the application of cork powders to TF significantly increased the persistence of wine; however, the scores obtained were significantly lower than the persistence of T0 (Table 6).

3.4 Impact of wine chemical composition on sensory profile of red wine treated with extractive free and ethanol impregnated cork powder and application doses

The sensory scores provided by the expert panel for aroma (Figure 6), taste and tactile/textural descriptors (Figure 7) and the chemical composition of wines, concerning the abundance of headspace aroma compounds and phenolic compounds, respectively, were subjected to multiple factor analysis. From the variable map, it can be concluded that for the first and second factors, both groups of variables contribute almost equally (53 and 46%, and 36 and 64% for the sensory and chemical data for the first and second factors, respectively) (Figure 6b).

Figure 6.

Multiple factorial analysis of aroma sensory and chemical data: (a) representation of wine samples and clouds; (b) representation of groups (tables) of variables and (c) distribution of variables. VP-free (T0) and VP-spiked (TF) red wines and after treatment with natural cork and dichloromethane and ethanol extractive free cork after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL, CKFI75250 and CKFI75500, respectively). Centroid (¡); sensory data (Δ); chemical data (◊). AcEt, ethylacetate; Ac3 MetBut, 3-methylbutan-1-ol acetate; 3-MetButol, 3-methylbutan-1-ol; EtOct, ethyl octanoate; EtDec, ethyl decanoate; DiEtSuc, diethyl succinate; PhEt, 2-phenylethanol; 4-EG, 4-ethylguaiacol; 4-EP, 4-ethylphenol; OctAc, octanoic acid; DecAc, decanoic acid; DodAc, dodecanoic acid.

Figure 7.

Multiple factorial analysis of taste and tactile/textural sensory data, phenolic compound chemical data and volatile phenol headspace abundance: (a) representation of wine samples and clouds; (b) representation of groups (tables) of variables and (c) distribution of variables. VP-free (T0) and VP-spiked (TF) red wines and after treatment with natural cork, dichloromethane and ethanol extractive free after air removal and ethanol impregnation (CKNI and CKFI) and cork powders with a particle size below 75 μm at two application doses (250 and 500 g/hL, CKFI75250 and CKFI75500, respectively). Centroid (¡); sensory data (Δ); chemical data (◊); VP headspace abundance (●). TotPhe, total phenols; FlavPhe, flavonoid phenols; t-CaftAc, trans-caftaric acid; CoutAc, coutaric acid; Del-3-Glc, delphinidin-3-O-glucoside, Cya-3-Glc, cyanidin-3-O-glucoside, Peo-3-AcGlc, peonidin-3-O-(6-O-acetyl)-glucoside; VPs, volatile phenols; 4-EP, 4-ethylphenol; 4-EG, 4-ethylguaiacol.

The phenolic negative attribute and the 4-EP and 4-EG headspace abundance were positively correlated with F1, showing that the reduction of the headspace abundance of 4-EP and 4-EG caused by CKNI, CKFI, CKFI75250 and CKFI75500 was important for the decrease of this wine defect. The fruity and floral positive attributes were negatively correlated with F1, showing that the decrease of the headspace abundance of these VPs was important for their perception. However, the abundance of the other headspace aroma compounds was also important for their perception, as they also present negative F1 score. These results are in accordance with previous works that verified that the absence of wine aroma defects, including VPs, was more important for the final wine aroma profile, where that negative off-odorants exert a strong aroma suppression impact on fruity aroma [20, 21, 24, 61, 66].

The phenolic composition of wines although changed significantly, especially after application of the CKFI75 at the two levels, the decrease was not high; nevertheless, significant differences were observed for bitterness, astringency, balance and persistence by sensory analysis, parameters usually linked to the phenolic composition of wines [67]. By the phenolic composition of treated wines, the headspace abundance of 4-EP and 4-EG was also used for MFA, because is actually known that the aroma can interact with the perceived bitterness and astringency of foods, where wines are included [24, 67]. The first factor was important to describe the sensory and VP headspace abundance variables (Figure 7b). In the case of the chemical variables, only the second factor was important for its description. The correlation maps of observations and variables (Figure 7c) show that the persistence, body and balance attributes were correlated with F1 in the negative direction. However, acidity, bitterness and astringency attributes were correlated with F1 in the positive direction, and there was also a positive correlation between VP headspace abundance with this factor. The correlation of bitterness and astringency, unpleasant wine sensory attributes, with the headspace abundance of VPs, responsible for the negative phenolic aroma, can be explained by the relationship between several aroma compounds with the bitterness and astringency of foods, shown also for wine [24, 68]. The significant decrease observed in some phenolic compounds after application of ethanol impregnated cork-powders does not seem to be responsible for the change in the taste/tactile descriptors observed after wine treatment.

The results obtained from MFA supported the results from sensory analysis of the wines obtained after treatment with the different ethanol impregnated cork powders at the applied doses, highlighting the efficiency of extractive free cork-powders, especially cork powder with a lower particle size at 250 g/hL application dose (CKFI75250), for decreasing the levels of 4-EP and 4-EG in wines and for recovery of fruity and floral aroma attributes. A decrease in phenolic, bitterness and astringency attributes was also observed. The results obtained for visual (colour), aroma, taste and tactile/textural descriptors determined by the expert panel, validated by the wine chemical composition after treatment with ethanol impregnated cork powders show that the wine treated with CKFI75250 resulted in a significant increase in the sensory quality compared to TF, although not identical to T0 wine. This is explained by the efficient removal of VPs and no negative impact on the wine phenolic composition and a lower impact on the headspace aroma compounds when compared to CKFI75500.

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4. Conclusions

Optimised cork powder can be a new, cheap, sustainable and efficient fining agent for removal of VPs from wines presenting the unpleasant “Brett character”. Its efficiency is shown by the capacity to adsorb significant amounts of 4-EP and 4-EG from a real red wine matrix, presenting a lower impact on the headspace positive aroma compounds when compared to other oenological solutions, already tested. The low impact on the phenolic composition of wines, especially on the monomeric anthocyanins, makes its impact on wine colour limited. Contaminated wines treated with optimised cork powder (extractive free and solvent impregnation) show a significant decrease of the negative phenolic attribute and a significant increase in the positive sensory fruity and floral attributes. This natural product can, in the near future, represent a new oenological fining solution with low environmental impact, contributing to a more sustainable wine industry.

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Acknowledgments

We acknowledge Aveleda SA for supplying wine, SAI Enology for providing CKP samples and Lisete Fernandes for the SEM images We appreciate the financial support provided to CQ-VR (PEst-OE/QUI/UI0616/2014) by FCT and COMPETE.

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Conflict of interest

No conflict of interest.

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Written By

Luís Filipe da Mota Ribeiro, Maria Fernanda Gil Cosme Martins and Fernando Hermínio Ferreira Milheiro Nunes

Reviewed: 07 March 2019 Published: 23 May 2019