Print version ISSN 0104-6632
Braz. J. Chem. Eng. vol.23 no.2 São Paulo Apr./June 2006
B. P. NobreI; R. L. MendesI, *; E. M. QueirozII; F. L. P. PessoaII; J. P.CoelhoIII; A. F. PalavraIV
IINETI, Departamento Energias Renováveis, Estrada do Paço do Lumiar, Phone +351 21-712-7192; fax +351 21-712-7195; 1639-038, Lisboa, Portugal. E-mail: firstname.lastname@example.org
IIUFRJ, Departamento de Engenharia Química, Escola de Química, Rio de Janeiro - RJ, Brazil
IIIISEL, Departamento de Engenharia Química, Lisboa, Portugal
IVIST, Departamento de Engenharia Química, Lisboa, Portugal
Supercritical CO2 extraction of the pigments from Bixa orellana seeds was carried out in a flow apparatus at a pressure of 200 bar and a temperature of 40 ºC at two fluid flow rates (0.67g/min and 1.12g/min). The efficiency of the extraction was low (only about 1% of the pigment was extracted). The increase in flow rate led to a decrease in pigment recovery. A large increase in recovery (from 1% to 45%) was achieved using supercritical carbon dioxide with 5 mol % ethanol as extraction fluid at pressures of 200 and 300 bar and temperatures of 40 and 60 ºC. Although the increase in temperature and pressure led to an increase in recovery, the changes in flow rate did not seem to affect it. Furthermore, two plug flow models were applied to describe the supercritical extraction of the pigments from annatto seeds. Mass transfer coefficients were determined and compared well with those obtained by other researchers with similar models for the supercritical extraction of solutes from plant materials.
Keywords: Supercritical carbon dioxide; Bixa orellana seeds.
Annatto (Bixa orellana) is a tropical tree whose seeds produce pigments with hues from yellow to red. Among other applications, these colours are used in the food industry to improve cheese, margarine and butter. One of the main pigments in the pericarp of the seeds is the carotenoid bixin (C25H30O4), which is one of the main natural colours (Scotter et al., 1994) and is found only in this plant. Chemically it is the mono-methyl ester of the dicarboxylic acid norbixin, another important pigment found in annatto seeds.
While this compound is soluble in oils upon heating and weakly soluble in supercritical CO2 (Nobre et al., 2002), norbixin is soluble in water and insoluble in supercritical CO2 (Degnan et al., 1991). Commercial extracts of oil-soluble annatto pigments are obtained from the seeds by several processes, such as suspension in oil, mechanical processes and solvent extraction with chloroform, dichloroethane and acetone (Preston and Rickard, 1980). Thecommercial preparations of annatto colours with organic solvents have the disadvantages of small concentrations of pigments and a residual toxic solvent in the product. Suspensions of annatto pigments in vegetable oil are more concentrated but can contain several degradation products due to the fact that high temperatures (>100 ºC) are used in the extraction process (McKeown and Mark, 1962; Reith and Gielen, 1971). Supercritical extraction with CO2 could be a good alternative to avoid these problems (Mendes et al., 2003).
Studies of Annatto pigment extraction have been carried out using supercritical CO2 (Degnan et al., 1991; Chao et al., 1991) and CO2 modified with several entrainers (methanol, chloroform and acetonitrile) (Anderson et al., 1997). It was shown that the entrainers increased the efficiency of extraction.
The objective of this work was to carry out supercritical fluid extraction of pigments from annatto seeds with CO2 and CO2 modified with ethanol and to assess the effects of temperature, pressure and solvent flow rate on the extraction yield and to propose a model to describe supercritical extraction.
MATERIALS AND METHODS
Carbon dioxide (99.998% purity) and carbon dioxide modified with 5 mol % ethanol were purchased from Air Liquide (Portugal). Annatto seeds and bixin were supplied by Universidade Federal do Rio de Janeiro (Nobre et al., 2002). Chloroform (p.a.), methanol (HPLC grade), acetic acid (p.a) and hexane (p.a) were purchased from Merck.
The pigment content of the seeds was determined by a method using organic extraction (McKeown and Mark, 1962), which consists in repeated extraction of the seeds with chloroform, up to total extraction of the colour. The total pigment content was determined using the Lambert-Beer law, measuring the absorbance of the solution at 501 nm [absorptivity 282.6 L/(g.cm)]. Whole seeds and ground seeds were analysed, with similar results for both conditions.
The seed oil content was quantified by gravimetric analysis, evaporating until dry 5 ml portions of the total volume of the organic extraction solution. On the other hand, the bixin concentration in the seeds was determined by analysing by HPLC (see below) the solution obtained with organic extraction of the seeds.
The supercritical measurements were carried out in a flow-type apparatus thoroughly described in a previous paper (Mendes et al., 1995). In this apparatus, the metering pump compresses the liquid solvent to the desired pressure, which is controlled by a back-pressure regulator. In order to guarantee that the fluid reaches the extraction vessel at the desired temperature, the fluid passes through a coil immersed in a temperature-controlled water bath. After passing the seed bed (2 g) contained in a 5cc cylindrical extraction vessel (id: 7.9mm) the fluid is expanded to atmospheric pressure through a three-way valve, and the extract precipitates in the glass wool placed inside the cooled glass U-tube. Gas flow rate is monitored by a rotameter and total volume of gas is measured with a wet test meter.
The extracts were collected by washing the glass wool, the inside of the three-way valve and the expansion tubing with chloroform containing 0.2 wt. % of BHT. The total pigment content was quantified by spectrophotometry. For the supercritical extraction measurements, fractions of 10 to 20 L of expanded gas were collected during extraction. Two flow rates were tested: 0.67g/min and 1.12g/min.
To assess the amount of pigment extracted, UV-Visible spectra were run between 300 and 700 nm and the concentration of pigment was determined using the Lambert-Beer law, measuring the absorbance at 501 nm.
The collected solutions were also analysed by HPLC. The system consisted of a liquid chromatograph, Hewlett Packard 1100 series, with a UV/VIS detector adjusted to 501 nm. A mobile phase of methanol and 2% acetic acid (87:13, v/v) was used at 1 ml/min with the stationary phase Nova Pak C18 column.
The quantification of the total supercritical extract (oils) for each seed batch was determined by gravimetric analysis, weighing the seeds before and after each experiment.
RESULTS AND DISCUSSION
Supercritical CO2 extraction of pigments from annatto seeds was carried out at 200 bar and 40 ºC. The recoveries obtained were low and decreased with the fluid flow rate (Fig. 1). The concentration of pigments in the extracted oil (about 0.4 %) was much lower than that obtained using chloroform as extraction solvent.
In Figure 2 the changes in concentration of the pigment during extraction is represented for the lower flow rate, as is the solubility of bixin at 200 bar and 40ºC.
The initial concentration of pigments is much higher than the solubility of bixin at the same pressure and temperature. That concentration decreases during extraction until the solubility value of the bixin is reached. The major component of the pigments in the seeds is cis-bixin (about 69 wt. %). The composition of the pigments in the supercritical extracts was near this value, although for the first fractions collected there was an increase in the concentration of bixin (about 75 wt. %) for several extraction conditions.
Whole seeds were submitted to extraction with carbon dioxide modified with ethanol at temperatures of 40 ºC and 60 ºC, pressures of 200 bar and 300 bar and flow rates of 0.67g/min and 1.12g/min. Milled seeds were also submitted to supercritical CO2 (200 bar/40 ºC). Recovery of the pigments did not increase with milling, possibly due to the location of these compounds at the surface of the seeds.
However, it was verified that this recovery increased with temperature at a constant pressure and with pressure at a constant temperature for the same flow rate (Fig. 3).
In Figure 4 the recovery of pigments by extraction using CO2 plus ethanol is represented. It can be verified that recovery practically does not change with flow rate for a large extent of the extraction (at least up to 30% of the pigments are obtained). This means that pigment extraction is limited by the equilibrium between the solid and fluid phases with values of concentration near or above the values of the solubility of bixin in this solvent mixture on the initial part of the curve (Fig. 5). This behaviour is quite different from that shown by supercritical extraction using pure CO2 (Fig. 1), in which extraction is limited by the intra-particle resistance to mass transfer. Ethanol can have two effects: one as entrainer, increasing the solubility of the pigments, and the other one as modifier of the mass transfer regime (easing the release of bixin from the seed pericarp).
In Figure 6 the changes in concentration of the pigments (mainly bixin) during extraction at a pressure of 200 bar, a temperature of 40 ºC and a flow rate of 0.67g/min is shown. The values are compared with the solubility of bixin in CO2 plus ethanol, at the same pressure and temperature.
Initially, the concentration is higher than that of bixin, possibly due to the effect of entrainment the triglycerides extracted with the pigments and also to the presence in the seeds of small amounts of degradation products (C17 yellow pigment, for instance). There is a short interval in which the values are similar to those for solubility of the compound, and after depletion of part of the bixin from the bed, the concentration decreases monotonously.
The behaviour of the two solvent systems (carbon dioxide, pure or with ethanol) in extracting the pigments (namely bixin) from annatto seeds is different in the recoveries obtained and in the mass transfer mechanisms. But a similar plug flow model (Sovovà, 1994b) can be applied to both situations. Important developments of models to represent supercritical fluid extraction have recently been published. These models deal with the extraction of vegetable oils (Reverchon and Marrone, 2001) and of oil from rosehip seeds (del Valle et al., 2004).
In the present work, it is assumed that the axial dispersion is negligible and that the properties of the solvent and seed bed remain unaltered. It is also assumed that the pigments are a single solute. When recovery is represented against time for extraction with pure CO2, the points fall on a common curve for the two flow rates (Fig. 7). On the contrary, with CO2 plus ethanol, the curve corresponding to the higher flow rate is above that of the lower flow rate (Fig. 8). In the former case (pure CO2), it is appropriate to assume that intra-particle resistance to mass transfer controls the extraction. In the latter case (CO2 plus ethanol), it is also appropriate to assume that the solvent film controls extraction. In both models, overall mass transfer coefficients are determined, an internal one for the extraction with pure CO2 and an external one for the system with ethanol.
The model can be represented by the following set of partial differential equations (PDE):
For the first system (internal mass transfer):
For the second system (external mass transfer):
The initial and boundary equations are
In these equations, y is the concentration in fluid phase, x (kg/kg) is the concentration in solid phase (solute-free), x0 is the initial concentration of extractable pigments, u (m/s) is the superficial velocity, h (m) is the height of the extractor, r is the solvent density (kg/m3), e is the bed porosity, rs (kg/m3) is the solid density, y* (kg/kg) is the equilibrium concentration of pigment in the supercritical fluid, x* (kg/kg) is the equilibrium concentration in the solid at the solid-fluid interface, ApKf (s-1) is the overall external mass transfer coefficient and ApKs (s-1) is the overall internal mass transfer coefficient. x0 was determined asymptotically from the extraction curves when the supercritical extraction was only carried out with carbon dioxide and it was determined through an extraction of pigments from annatto seeds using chloroform when the supercritical solvent was carbon dioxide plus ethanol.
The set of two PDEs was transformed into one of 2n of ordinary differential equations (ODEs), corresponding to a division of the plug flow extractor in n stages of perfect mixing. A Runge-Kutta method of the 4th order was used to solve the 2n system of ODEs.
For the supercritical solvent without entrainer, for which only the internal mass transfer is considered, it is necessary to know how y relates to x* (Reverchon, 1996). Another approach, which was used in the present work, is to consider x* negligible, taking into account that the resistance to internal diffusion is much higher than the resistance to solvent diffusion (Sovovà, 1994a).
For the supercritical solvent with ethanol, for which an external mass transfer coefficient is determined, it is necessary to know y*. This concentration was determined extracting pigments previously separated from the seeds and mixed with glass beads, using CO2 plus ethanol at a pressure of 200 bar and a temperature of 40 ºC (Nobre et al., 2003). It was found to vary during extraction (Fig. 7), and it was related to the corresponding concentration of the pigments in the seeds under these conditions of pressure and temperature, as shown in Eq. 7.
In Table 1 the parameters used in the application of the models are shown and in Figure 8 the change in extraction as a function of time is shown for the two flow rates at the same pressure and temperature. The lines represent the calculated values from the plug flow model, assuming that the extraction is controlled by the solvent film around the seeds.
The values determined for the external mass transfer coefficients (Table 2) are comparable to the values known for several plant materials (Sovovà, 1994b). On the other hand, the internal mass transfer coefficients (Table 2) are also of the same order of magnitude as those indicated for extraction of solutes from the same plants. Moreover, the coefficients calculated in this work show a good agreement with those found in supercritical carbon dioxide extraction of b-carotene from Dunaliella salina (Mendes et al., 2000).
The efficiency of supercritical carbon dioxide extraction of pigments from annatto seeds was low. When the flow rate of supercritical solvent increased, the recovery of pigments decreased, possibly due to resistance to mass transfer inside the seed pericarp. A high recovery of pigment was achieved when the mixed solvent (CO2+ethanol) was used. Moreover, this recovery didn't decrease with fluid flow rate and increased with pressure and temperature. The milling of the seeds had no effect on extraction.
An unsteady plug flow model was able to represent adequately the supercritical fluid extraction of the pigments from annatto seeds. When only CO2 was used an internal mass transfer coefficient was determined. On the other hand, when CO2 mixed with ethanol was used, extraction was controlled by solvent film. In this case, external mass transfer coefficients, which increased with flow rate, were calculated.
The calculated mass transfer coefficients compare well with those determined by other researchers for the supercritical fluid extraction of several solutes from plant materials.
B. P. Nobre thanks FCT (Portugal) and F. L. P. Pessoa and E M. Queiroz thanks CAPES for the research grant.
|y||concentration in fluid phase|| |
|x||concentration in solid phase|| |
|x0||initial concentration of extractable pigments|| |
|u||superficial velocity|| |
|h||height of the extractor|| |
|y*||equilibrium concentration of pigment in the supercritical fluid|| |
|x*||equilibrium concentration in the solid at the solid-fluid interface|| |
|ApKf||overall external mass transfer coefficient|| |
|ApKs||overall internal mass transfer coefficient|| |
|r||solvent density|| |
|e||bed porosity|| |
|rs||solid density|| |
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Received: October 20, 2004
Accepted: March 5, 2006
* To whom correspondence should be addressed