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The present work deals with the use of iron/sulfur-oxidizing bacterium Acidithiobacillus ferrooxidans for the desulfurization of a coal sample from Assam, India. The coal sample contains 3.87% w/w of organic sulfur, 1.4% w/w pyritic sulfur, and 1.29% w/w of sulfate sulfur which altogether are contributing to its total sulfur content of 6.56% w/w. The microbial process followed the oxidative-desulfurization mechanism for the removal of sulfur from the coal sample. The bacterium performed cleavage of the sulfide bonds in pyrite to release the inorganic sulfur. Mass spectroscopic analysis revealed that the bacterial strain A. ferrooxidans performed oxidative desulfurization of a model sulfur-containing organic compound dibenzothiophene to 2-hydroxy biphenyl through the formation of dioxy-dibenzothiophene. A. ferrooxidans cells played the catalytic role to release the sulfur present in organic and inorganic form in the coal sample. The microbial desulfurization process conducted in a shake flask scale (500 mL) removed about 79% of total sulfur from the coal sample in 14 days. [ABSTRACT FROM AUTHOR]

Mineralogically distinct coal samples respond differently to microbial attack. In the present study, a mixed meso-acidophilic bacterial consortium predominantly comprising of Acidithiobacillus ferrooxidans strain was investigated for its biodesulphurization abilities for three distinct sulphur bearing samples (Goa CPC, Rajasthan Lignite, Assam Coal) of Indian origin in iron (9K+) and iron-free (9K−) media. A media devoid of Fe (II) iron was more effective for sulphur removal with maximum desulphurization of 45.19% for Assam coal followed by 36.8% for Rajasthan Lignite and 23.38% for CPC respectively. The proximate analysis, FTIR patterns and XRD analysis of the samples provided better insights into understanding the mineralogical and compositional changes in the coal matrix. Owing to the higher efficiency, Assam coal was additionally subjected to further optimization studies and characterization of the treated coal through TGA. The study indicated that the gross calorific values for all the samples increased following microbial treatment in 9K− media thereby providing a scope for further scale-up studies. [ABSTRACT FROM AUTHOR]

Since the sulfur specific cleavage is vital for the organic sulfur removal from fossil fuel, we explored potential bacterial strains of MTCC (Microbial Type Culture Collection) to desulfurize the Dibenzothiophene (DBT) through C-S bond cleavage (4-S pathway). MTCC strains Rhodococcus rhodochrous (3552), Arthrobacter sulfureus (3332), Gordonia rubropertincta (289), and Rhodococcus erythropolis (3951) capable of growing in 0.5 mM DBT were examined for their desulfurization ability. The presence of dsz genes as well as the metabolites was screened by polymerase chain reaction (PCR) and HPLC, respectively. All these strains showed > 99% DBT desulfurization with 10 days of incubation in minimal salt medium. From the HPLC analysis it was further revealed that these MTCC strains show differences in the end metabolites and desulfurize DBT differently following a variation in the regular 4-S pathway. These findings are also well corroborating with their respective organization of dszABC operons and their relative abundance. The above MTCC strains are capable of desulfurizing DBT efficiently and hence can be explored for biodesulfurization of petrochemicals and coal with an eco-friendly and energy economical process. [ABSTRACT FROM AUTHOR]

In the current era, the alarming rate at which coal is being burned as a fuel is causing concern with regard to the release of sulphur oxides. According to reports, global coal consumption has increased by 0.4% in 2014. While countries like UK, Ukraine etc. have witnessed a decline in coal consumption, some others like India, China, Africa and North America have increased their use of coal to meet the energy requirements of the growing human population. The increasing use of coal has led to extensive investigations for finding an ecofriendly clean coal technology. Dibenzothiophene (DBT) and some of its alkylated derivatives present in the form of organic sulphur in coal have received a great deal of attention in the past few years because of their recalcitrant nature. Considering the economic and environmental prospects, biodesulphurization is being regarded as an effective tool for the degradation of DBT, with concomitant application towards sulphur removal from coal. Owing to the importance of microbial applications towards production of clean coal, the present review discusses some of the recent findings in the area of DBT biodegradation. In addition, current advances in coal biodesulphurization are reviewed, concluding with a consideration of future prospects for the rapidly growing energy sector. [ABSTRACT FROM AUTHOR]

A native isolate, 9C, identified as Rhodococcus ruber (Genbank Accession number – KY029073) was studied for dibenzothiophene degradation and subsequent bio-desulphurization of three different sulphur bearing materials (NE coal containing organic sulphur; lignite containing pyritic sulphur and a calcined petroleum-coke) of Indian origin. The isolate could degrade 0.25 mM DBT through the 4S pathway within 7 days. Preliminary studies for sulphur removal using the 9C isolate indicated NE coal to be more amenable (29% sulphur removal) followed by Lignite (15.87%) and CPC (14.83%) respectively. Characterization through XRD and FTIR along with the proximate and ultimate analysis of all the samples provided more insights into the changes in calorific values as well as the chemical constitution of the samples following microbial treatment. Owing to the amenability of NE coal, the effect of time, size fraction and pulp density were optimized. The best bio-desulphurization conditions for NE coal indicated 36% total sulphur removal (organic–53%, pyritic–18% and sulphate sulphur–14% respectively). Analytical characterization studies confirmed that the energy value of the NE coal was not affected due to biodesulphurization, rather it contributed towards an increase in gross calorific value from 6698 cal/g to 6812 cal/g following microbial treatment. [ABSTRACT FROM AUTHOR]