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Química Nova

Print version ISSN 0100-4042On-line version ISSN 1678-7064

Quím. Nova vol.27 no.2 São Paulo March/Apr. 2004

http://dx.doi.org/10.1590/S0100-40422004000200004 

ARTIGO

 

Quantitative analysis of phenol and alkylphenols in Brazilian coal tar

 

 

Elina Bastos CaramãoI; Irajá do Nascimento FilhoII, *

IInstituto de Química, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9.500, 91501-970 Porto Alegre - RS
IIDepartamento de Química, Universidade Regional Integrada do Alto Uruguai e das Missões, Av. Sete de Setembro, 1621, 99700-000 Erechim - RS

 

 


ABSTRACT

The main purpose of this work is the identification and quantification of phenolic compounds in coal tar samples from a ceramics factory in Cocal (SC), Brazil. The samples were subjected to preparative scale liquid chromatography, using Amberlyst A-27TM ion-exchange resin as stationary phase. The fractions obtained were classified as "acids" and "BN" (bases and neutrals). The identification and quantification of phenols, in the acid fraction, was made by gas chromatography coupled to mass spectrometry (GC/MS). Nearly twenty-five phenols were identified in the samples and nine of them were also quantified. The results showed that coal tar has large quantities of phenolic compounds of industrial interest.

Keywords: coal tar; phenols; GC/MS.


 

 

INTRODUCTION

Coal is used in industries as a natural source of energy, mainly in gasification processes. An important by-product of the thermal treatment of this matrix is coal tar, considered today as an environmental by pollutant material1. On the other hand, substances that have wide application in the chemical and pharmacological industries can be found in this matrix2. Phenol and substituted phenolic compounds are widely used in the production of polymers, drugs, dyes, explosives, pesticides, stabilizers and antioxidants3,4.

However, when phenolic compounds are discharged into the environment they can represent a serious hazard, mainly by the contamination of superficial and underground waters. Thus, at trace levels they can cause prejudice to the majority of the aquatic organisms and can induce bioaccumulation in the food chain4-6. Phenolic compounds are also pointed out as important co-carcinogenic substances3,7. They can considerably increase the effects of a secondary carcinogen (a substance that does not form cancerous tumors at the introduction point but in remote points and, sometimes, in specific organs).

The importance of co-carcinogenic properties of phenolic compounds is higher than that normally assigned to them, since some kinds of human cancer, due the exposition to certain materials, can results from small quantities of primary carcinogens (which promote animal cancers at the application point) and relatively higher quantities of co-carcinogens3.

The presence of phenolic compounds in the environment is preoccupying not only due to the knowledge of their dangerous facets but (maybe mainly) from some indications that these compounds can be genotoxic and there is a lack of enough data to discard with security, this possibility3.

Thus, the investigation of components of coal tar that can promote hazardous effects to human health and to the environment and, on the other side, the social and economic advantages that result from industrial utilization of these compounds, where a decrease the costs of medical treatment, for example, must be carefully considered.

Coal is an alternative energy source that will assume a future key position with the decrease of oil production. The southern region of Brazil is an important coal producer and consumer, mainly in thermoeletric power plants. In spite of this, there is a lack of Brazilian work focusing on the phenolic composition of coal tar and its utilization as feedstock for other industries. In this work phenols were extracted by ion-exchange liquid chromatography and quantified by GC/MSD using the internal standard method.

 

EXPERIMENTAL PART

Coal tar samples were obtained from the ceramic industry Eliane (Cocal-SC/Brazil). Reagents and solvents utilized in this work were of p.a. grade, purchased from Merck S.A. The following standards (Sigma-Aldrich) were used: phenol, o-cresol, p-cresol, m-cresol, 2-ethylphenol, 2,5-dimethylphenol, 4-ethylphenol, 2,3-dimethylphenol, 3,4-dimethylphenol. 4-n-propylphenol was used as internal standard.

Resin treatment

10 g of Amberlyst A-27TM resin (Sigma-Aldrich) were mixed with 50 mL of a mixture of NH4OH and methanol diluted in methanol (1+9, v/v). This mixture was stirred for 3 min and, after a few minutes at rest, the resin was washed in a sinterined glass funeel with the following solvents: methanol (25 mL), water (until pH 7), acetone (25 mL) and n-hexane (25 mL).

Sample fractionation

200 mg of the coal tar sample were dissolved in dichloromethane. This solution was placed at the top of a glass column (15 cm long x 11 mm i.d.) packed with 10 g of Amberlyst A-27TM ion-exchange resin previously treated as described above. The basic and neutral compounds were eluted with 60 mL of n-hexane and the acidic fraction (phenolic compounds) was eluted with 70 mL of a mixture of formic acid/diethyl ether (1+6 v/v). The acidic fraction was dried with anhydrous sodium sulfate and its volume was reduced to 1 mL under a gentle steam of ultra-pure nitrogen. The acid fraction was derivatized with bis-trimethylsilylacetamide (BSA)8 to improve the chromatographic performance of the phenolic compounds9-12. The extraction procedures were made in triplicate and each acid fraction was injected three times (resulting 9 injections) in the GC/MS system (SCAN mode). These injections were made for specify the single ions for the quantitative analisys (SIM mode).

Quantitative analysis

Individual stock solutions were made with each standard phenolic compound at 1,000 mg L-1 in dichloromethane. The standard compounds were at least 99% pure. A spike solution (also in dichloromethane) at 100 mg L-1 of all the standards was made from the stock solution. An aliquot of this spike solution was submitted to the extraction process and 1 µL of the extracts were injected in the GC/MS system, for recovery calculations. Real samples were not used for recovery tests. All the experiments were made in triplicate. The GC/MS analysis conditions are described in Table 1.

 

 

RESULTS

Figure 1 presents the Total Ion Current (TIC) chromatogram for the samples acid fraction. The identification of the numbered peaks is presented in the Table 2.

 

 

 

 

Twenty-three phenols were tentatively identified, as their trimethylsilyl derivatives; nine of then had their identities confirmed by co-injection of standards.

The recoveries of phenols ranged from 59.9% for phenol to 99.9 % for 4-ethylphenol, while the detection limit varied from 3 to 12 mg kg-1 (Table 3). The low recovery of phenol can be explained by its high volatility.

The amount of phenols in the samples varies from 8.13 mg kg-1 for 2-ethylphenol to 190.70 mg kg-1 for 4-ethylphenol (Table 3).

 

CONCLUSIONS

The results of the quantitative analysis demonstrate that the methodology adopted is simple and adequate for enrichment of phenolic compounds in this kind of sample.

The quantities of phenols compounds found in the samples justify their extraction for utilization as feedstock for the drug, paint, dye and other chemical industries, mainly with respect to phenol, the cresol isomers and 4-ethylphenol, that are the predominant phenols in the samples.

The extraction of these compounds from coal tar samples, in the future, will permit a decrease in feedstock material importation, resulting in a redution in manufactured product costs as well in environmental preservation.

 

ACKNOWLEDGMENT

The authors thank to Dr. M. Di Luccio for relevant suggestions and to CAPES, FAPERGS and CNPq for financial support.

 

REFERENCES

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9. Creaser, C. S.; Koupai-Abyasani, M. R.; Stephenson, R. G.; J. Chromatogr. 1989, 478, 415.        [ Links ]

10. Freedman, R. W.; Croitoru, P. P.; Anal. Chem. 1964, 36, 1389.        [ Links ]

11. Green, J. B.; Shirley, K. T. Y.; Vrana, R. P.; J. High Resolut. Chromatogr. 1989, 478, 415.        [ Links ]

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Recebido em 13/1/03
aceito em 29/10/03

 

 

* e-mail: iraja@uri.com.br

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