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Acute toxicity evaluation of several compounds involved in fossil fuels biodesulphurisation studies

dc.contributor.authorAlves, Luís
dc.contributor.authorPaixão, Susana M.
dc.contributor.authorGírio, Francisco
dc.date.accessioned2010-07-28T10:34:37Z
dc.date.available2010-07-28T10:34:37Z
dc.date.issued2009-12-04
dc.description.abstractThe increasing use of fossil fuels has led to increased emissions of sulphur oxides into the air, which is a major cause of acid rain. Legislation already adopted in 2009 stipulates that the maximum level of sulphur allowed in fuels is only 10 ppm. The process of hydrodesulphurization (HDS) used in refineries is based on very expensive physico-chemical techniques, and has limitations in the removal of organic sulphur. As for stricter legislation on the maximum levels of sulphur in fossil fuels, the most HDS recalcitrant compounds needs to be removed. This implies an increase in the intensity of the physical-chemical treatment and inherently its associated costs. As a result, the recalcitrant compounds to HDS represent a significant barrier to the achievement of very low levels of sulphur in some petroleum fractions. The alternative to the physical-chemical treatment could be the use of biological processes (biodesulphurisation) which is more effective for the desulphurization of fossil fuels, especially as the removal of sulphur covalently bound to organic matrices. The biodesulphurisation (BDS) occurs in more mild conditions of operation under conditions of atmospheric pressure and temperature, giving greater specificity of reaction due to the nature of the biocatalysts, not requiring molecular hydrogen. Thus, in the last 15 years there has been an increase of studies involving the use of microorganisms with the ability to specifically remove the HDS recalcitrant sulphur compounds. Several model compounds such as dibenzothiophene (DBT), DBT sulphone or benzothiophene (BT) are used in BDS studies to characterise organic sulphur in coal, coal tars and crude oils. The desulphurising microorganisms are able to remove the sulphur atom from these compounds and use it in their metabolism. However, such compounds are very toxic to the cells. The aim of this work was to evaluate the toxicity of several compounds used in BDS studies, such as DBT and its derivatives and organic solvents used to dissolve these hydrocarbons, to two typical desulphurising strains, namely: Gordonia alkanivorans strain 1B and Rhodococcus eritropolis strain D1. The toxicity bioassays evaluated the inhibitory effect of the studied compounds to the described bacteria by measuring the respiration rate (mg O2/l) under defined conditions in the presence of different concentrations of those compounds. The inhibitory or toxic effect of each chemical at a specific concentration is expressed as a percent of the baseline respiration rate. From these results the several IC50s were estimated and are described in Table 1. These toxicity values showed that strain 1B was less sensitive for almost all of the hydrocarbons, which is an important advantage considering the desulphurisation of fossil fuels process. On the other hand, strain 1B was more sensitive to dimethylformamide (DMF), a typical solvent used in BDS studies. However, a good correlation can be observed between IC50-1B versus IC50-D1 (IC50-D1 = 0.504 x IC50-1B + 2.84; r2 = 0.908, p < 0.05).pt
dc.identifier.citationAlves, L.; Paixão, S. M.; Gírio, F. M. Acute toxicity evaluation of several compounds involved in fossil fuels biodesulphurisation studies. In: III International Conference on Environmental, Industrial and Applied Microbiology, BioMicroWorld’ 2009, Lisboa, 2009, December 2-4, p. 369pt
dc.identifier.urihttp://hdl.handle.net/10400.9/873
dc.language.isoengpt
dc.subjectAcute toxicitypt
dc.titleAcute toxicity evaluation of several compounds involved in fossil fuels biodesulphurisation studiespt
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboapt
oaire.citation.titleIII International Conference on Environmental, Industrial and Applied Microbiology, BioMicroWorld’ 2009pt
person.familyNameAlves
person.familyNamePaixão
person.familyNameFERREIRA GIRIO
person.givenNameLuís
person.givenNameSusana M.
person.givenNameFRANCISCO MANUEL
person.identifier.ciencia-id561B-53A5-7359
person.identifier.ciencia-id7918-C133-C5FB
person.identifier.ciencia-idD51D-09A4-A2DC
person.identifier.orcid0000-0001-6245-775X
person.identifier.orcid0000-0003-0955-4467
person.identifier.orcid0000-0002-5376-8430
person.identifier.scopus-author-id6701310833
person.identifier.scopus-author-id6603112228
rcaap.rightsopenAccesspt
rcaap.typeconferenceObjectpt
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relation.isAuthorOfPublication.latestForDiscoveryb763d40e-827e-4b6b-949c-d6c8a7166cc5

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