The polyurethane foam obtained from vegetable oil is the foam differentiated from those that usually exist in the market, because the raw material is biodegradable, reducing environmental impact  . The polymerization of urethanes occurs during the synthesis of polyurethane foams due to the reaction of a compound with two or more isocyanates with a polyol  .
Ferreira (2006)  demonstrated the effectiveness of polyurethane foams, modified by the addition of sulfur powder and zinc oxide, as a practical filtering system and efficient for the removal of mercury and sulfur compounds from natural gas. The author also said that the polyurethane foams have their own characteristics that allow the passage of gas as open cells and a good homogeneity and pore distribution.
Textile dyes are organic compounds that impregnate the textile substrate fibers with different color during the dyeing process. Most effluents from the textile industry come from the dyeing stages, resulting in the degradation of the environment, because the dyes are resistant to biological treatments and have slow degradation kinetics  (Trombini and Doi, 2012).
The polluting potential of a small/medium-sized textile industry is estimated to be equivalent to the volume of waste generated by approximately 7000 to 20,000 people, according to (Moraes, Freire, Durán, 2000, p. 369 and Pereira, Freire, 2005, p. 131)  . Guaratini and Zanoni (2000)  add that due to their own nature, dyes are highly detectable to naked eyes and are visible in some cases even at concentrations as low as 1 ppm (1 mg/L). Indeed, a small amount of dye released into aquatic effluents can color the rivers and be easily detected by the public and authorities. The dyes can interfere in the process of photosynthesis in the rivers with huge impact to the environment  .
Since this is an unpublished study, no papers were found where polyurethane foams derived from vegetable oils were used in the adsorption of textile dyes. It was observed that the effectiveness of polyurethane foams obtained from vegetable oil for the adsorption of textile dyes is an excellent viable alternative to avoid the contamination of textile dyes in the aquatic environment.
2. Materials and Methods
Randomly, the choice of dyes was not restricted to any criterion such as color, hue and solubility, and there was only restriction regarding the physical state that in this context was delimited to dyes in the solid state because they are more stable and with less potential of sample degradation. It was collected water samples from the Effluent Treatment Station of a company founded in 1984 in the city of Passos, state of Minas Gerais in Brazil that uses industrial dyeing.
The dyes available for sampling belonged to the line of direct dyes because they are economically feasible and easy to apply, as well as used in different types of fabric. Thus, five different samples were selected: Green Quimacel Concentrated Light, Violet Quimacel Light B, Rubinol Quimacel Light BL, Yellow Quimacel Light GL and Orange Quimacel Light 2G 250. The international registrations of these dyes are Green-1, Violet-51, Red-83, Yellow-86 and Orange-39, respectively.
The dyes were prepared in aqueous solution. Due to the high solubility, the solution was then prepared with concentrations close to 1 mol・L−1, 2 mol・L−1, 3 mol・L−1, 4 mol・L−1 and 5 mol・L−1.
2.1. Reagents and Solutions
Stock solutions 1000 mg・L−1 of dyes provided by the company were prepared by being dissolved in distilled water. Subsequently, the standard solutions were prepared by successively diluting at concentrations close to 1 mol・L−1, 2 mol・L−1, 3 mol・L−1, 4 mol・L−1 and 5 mol・L−1. All reagents of analytical grade were used without prior purification. The stock solutions were stored in the refrigerator in amber glass bottles for a maximum of three weeks, later they were properly discarded.
The analytical solutions used were subsequently prepared from the dilution of the stock solutions in volumetric flask, the volume being filled with distilled water in a mixed bed column.
Polyurethane foam was made and supplied by the Group of Analytical Chemistry and Polymer Technology―GQATP of the Institute of Chemistry of São Carlos―IQSC/USP  .
The polyurethane was prepared by mixing the prepolymer and the polyol. The stoichiometric ratio for the polyurethane is 1:0.7 (prepolymer and polyol, respectively).
After curing, the polyurethane has approximately a specific mass of 0.0440 g/cm3 and a pore size equal to 0.7 μm.
2.2. Storage of Solutions and Effluent
Amber glass vials were used during the experiments. They are kept in a refrigerator at a temperature of approximately 12.0˚C ± 0.2˚C to prevent the decomposition of the dyes by the action of light, as well as variations in the concentration caused by the evaporation of the solvent.
2.3. Adsorption of Dyes
The amount of adsorption of dyes present in water was done by percolation in a thermostatted glass column. The results are shown in Figure 1. The polyurethane, with a known mass, was pressed in the form of powder between two solid foam disks containing two millimeters thick and 20 mm in diameter. 50 mL of sample was used for elution.
2.4. UV/V Is Absorption Spectrophotometry
The quantitative determinations of the dyes before and after percolation in the column containing the polyurethane foam, through UV/V is Spectrophotometry measurements uses quartz cuvettes of 1 cm optical path and deionized water as a reference.
The intensity in color of dye solution was calculated using the Lambert-Beer Law shown in Equation (1). A relation between absorbance, sample thickness
Figure 1. Thermostatted glass column used in the experiment. Source: Camargo, M.A.F., 2010  .
(optical path) and concentrations of the species they absorb was established.
where c is the concentration of the sample (mols・L−1), b the optical path (in centimeters) and ε (epsilon) as molar absorptivity (in L・mol−1・cm−1)  .
Scanning measurements were performed at wavelengths of 300 nm to 900 nm at 1nm intervals, with a maximum wavelength around 464 nm in the visible region expected, other wavelengths will be used depending on the type of dye provided for the experiments. Adsorption of the dyes in the polyurethane foam was monitored at the following wavelengths, Green-1 at 616 nm, Violet-51 at 546 nm, Yellow-86 at 634 nm, Red-83 at 643 nm and Orange at 399 nm, respectively. The measuring equipment was a UV-Vis Spectrophotometer, model Spectro Direct, Lovibond brand. The quantification was performed before and after elution in the foam, extending the measurement after passage through the foam for a period of 45 days in order to verify the stability of the dye in solution. The data collected in the tests were analyzed, seeking to verify the adsorption of textile dyes in polyurethane foams derived from vegetable oil.
3. Results and Discussions
Reliable results led to serial dilution of stock solutions until the absorbance value was less than or equal to 1. All serial dilutions started from the stock solution dyes with the lowest concentration (Figure 2). Three levels of concentrations were chosen, high, medium and low.
Absorbance readings were performed after each further elution until the foam saturated, i.e., ceased to adsorb the dye in solution.
The potential of hydrogen (pH) of the samples, seen in Figure 3, is an important parameter and was measured with the aim of characterizing each one of the dyes.
Note that, on average, Violet-51, Yellow-86 and Orange-39 dyes did not
Figure 2. High, medium and low concentrations of dye solutions used in the experiment.
Figure 3. pH curves of the selected dyes.
present great oscillations of the pH with the increase of the concentrations, remaining close to the average pH value.
The Green-1 dye presented a basic character with increased concentration, while the Red-83 presented acidic character.
3.1. Adsorption by Glass Column Percolation and Reading by UV/Vis Spectrophotometry
With an average molar absorptivity of 5422 L・mol−1・cm−1, the Green-1 dye had the best adsorption among all dyes presenting better variations, where there was a considerable difference between initial measurement and saturation measurement.
At high concentration (Figure 4), the variation was 0.296 nm units of absorbance, while at medium concentration (Figure 5), it was 0.068 nm and at low concentration (Figure 6), it was 0.015 nm. This shows that the more solute in the solution, the greater the adsorption of these dyes.
As it is shown in Figure 6, it took the low concentration 5 elutions to saturate the foam, since after the fifth elution, the absorbance remained the same. Whereas it took the low concentration 3 elutions to saturate, maintaining the absorbance in 0.124 nm after other elutions.
Figure 4. Dye adsorption at high concentrations.
Figure 5. Dye adsorption at medium concentration.
Figure 6. Dye adsorption at low concentration.
Violet-51 and Green-1 dyes were the only dyes where the stock solution 1, the lowest concentration, did not require dilution to obtain a high concentration in the spectra reading and adsorption percolation assays. All other dyes required at least one dilution.
The three concentrations of Violet-51 presented regular results when adsorbed, with 0.096 nm for high concentration; 0.067 nm for medium concentration and 0.031 nm for low concentration. All concentrations obtained considerable removal variations, taking into account the initial concentration of the sample, taking 7362 L・mol−1・cm−1 of molar absorptivity.
The saturation and stabilization of the foam at medium and low concentrations occurred at elutions 4 and 5, respectively, where, it was observed that, at these elutions the absorbances were maintained.
Yellow-86 proved to be a difficult substance to manipulate for both weighing and reading its spectrum. This is due to the high molecular dye weight, complicating the weighing in the preparation of the stock solutions and later, in the UV/Vis Spectrophotometry reading, where several serial dilutions were necessary for the absorbance to reach reliable values.
The least adsorbed dye was Yellow-86, presenting 2037 L・mol−1・cm−1 molar absorptivity. At high concentration it obtained a variation of absorbance of only 0.005 nm, while at medium and low concentrations it showed 0.003 nm. This also presented fast foam saturation, since in the highest concentration it took 4 elutions and in the lower 1 elution. At low concentration, 3 elutions were required for saturation.
Red-83 has a slightly lower molecular weight than Yellow-86, but still a high molecular weight and thus required serial dilutions to lower the concentration, being the dye that required a very high concentration lower than the others, reaching 1/32.
It had a molar absorbance of 6279 L・mol−1・cm−1. This dye also did not show a good adsorption, however it presented better than the worst dye, the Yellow-86. The absorbance variations expressed by the concentrations were 0.007 nm, 0.006 nm and 0.003 nm, respectively.
Also in similarity to the aforementioned dye, this also presented fast foam saturation, which one can speculate that the fast saturation of the foam would be correlated with the molecular weight.
While at high concentration, four elutions were required for the foam saturation, at medium concentration only 2 elutions were required, which was stabilized with an absorbance of 0.040 nm. At low concentration the foam saturated with only one elution with the absorbance remaining at 0.020 nm after further elutions.
Unlike the two dyes mentioned above: the Yellow-86 and the Red-83, the Orange-39 dye is the least dense, having the lowest molecular weight of the dyes in this study. This made the manipulation for the preparation of solutions and also for the realization of the reading of its spectrum easier, not requiring several serial dilutions.
With a molar absorptivity of 14,504 L・mol−1・cm−1, Orange-39 dye had absorbance change at its first concentration of 0.034 nm, whereas at medium concentration the foam saturated with an absorbance of 0.019 nm and at low concentration with 0.007 nm, as shown in Figures 4-6.
3.2. Analysis of the Gross Effluent
The collected effluent sample had a black color (Table 1), unpleasant odor and basic character, with a pH of 7.05. This is due to the mixture of soap, bleaches, softeners and of course, dyes. It was chosen to collect the dye without any kind of treatment, so it was collected from the first treatment pool.
In Figure 7, it was observed excellent adsorption of dye results present in the effluent, since there was a reduction of 0.508 nm in absorbance. This represents 50.95% of the amount of material removed from the effluent, making the results even more relevant when taking into account that the effluent is the amount of substances and dyes mixed.
It is concluded that polyurethane foam derived from vegetable oil is a viable solution for the reduction of textile dyes dispensed daily by the industries, as it presented excellent adsorption results, removing the dyes even when they were in extremely low concentrations.
Table 1. Absorbance values in textile effluent.
Figure 7. Adsorption curve of the untreated effluent at unknown concentration.
The results were satisfactory in the analysis of crude effluent, since this one showed reduction in the amount of dyes present in the sample. This result is still more relevant when one considers that the raw effluent sample is a mixture of various dyes.
This biodegradable foam obtained from renewable sources coupled to the principal receptor pipeline of the Effluent Treatment Station of the industries would considerably reduce the costs of treatments for the dye removal used in the various areas of dyeing as well as the reduction of physical space due to the dispensability of more pools for such treatments reducing thus the aggression to the environment.
 Ereno, D. (2003) Próteses de mamonas. Revista Pesquisa—Fapesp.