American Journal of Analytical Chemistry
Vol.5 No.6(2014), Article ID:45156,6 pages DOI:10.4236/ajac.2014.56044

Role of Infrared Spectroscopy in Coal Analysis—An Investigation

Manoj Balachandran

Department of Physics, Christ University, Bangalore, India

Email: manoj.b@christuniversity.in

Copyright © 2014 by author and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

http://creativecommons.org/licenses/by/4.0/

Received 25 February 2014; revised 27 March 2014; accepted 4 April 2014

ABSTRACT

Fourier transform infrared (FT-IR) spectroscopy is a widely used analytical technique for determining the different functional groups of a coal structure. This method, being able to reveal carbohydrogenated structures (aromatic and aliphatic) and heteroatomic functions (mainly oxygenated), as well as to detect the presence of minerals, is currently one of the most powerful techniques for coal characterization and thus is of paramount importance in the various utilization procedures of coal (industrial combustion, coke production processes, etc.). FT-IR study shows the presence of aliphatic -CH, -CH2 and -CH3 groups, aliphatic C-O-C stretching associated with -OH and -NH stretching vibrations and HCC rocking. It is conjectured that, the two-stage leaching using HNO3 followed by HF remarkably reduced the ash content as well as the minerals including Al, Si and Ca. The solubilization of samples with buffered EDTA could not eliminate the minerals in coal. The silicate and kaolinite bands showed a systematic lowering on EDTA and carboxylic acid treatment. The fungal leaching was most beneficial for aromatic molecules with different degrees of substitution. The intensity of bands due to carbonyl groups was increased, when treated with fungi, whereas that due to oxygen functional groups showed a reverse trend. The mineral bands due to silicates also decreased in intensity, on post treatment with fungal culture.

Keywords:Coal, Leaching, FT-IR, Bioleaching, Organic Acid

1. Introduction

By origin, coal is a heterogeneous material consisting both carbonaceous and inorganic material. The acceptance of it for a particular industry decisively depends on both of these constituents. The organic structure of coal can be regarded as consisting of heterogeneous aromatic structures, with aromaticity increasing from low to high rank coals. The organic part of coal also contains sulphur, oxygen, and nitrogen in functional groups. Fourier transform infrared (FT-IR) spectroscopy is a widely adapted analytical technique for determining the different functional groups in coal structure [1] -[6] . This technique, being able to reveal carbo-hydrogenated structures (aromatic and aliphatic) and heteroatomic functions (mainly oxygenated), as well as to perceive the presence of minerals, is presently one of the most powerful techniques for coal characterization and thus is of vital role in various utilization procedures of coal. The presence of mineral matter is considered as detrimental in coal utilization, preparation and transportation. Coal preparation is aimed at reducing the quantity of mineral matter and the efficient use of methods chosen depends on its concentration. They may exist as a separate entity or bonded with organic components of coal. Prior to the structural analysis, demineralization is essential, because minerals, silica in particular, would distort the functional groups which in turn affect the prominent characteristics of coals.

Though research on demineralization and characterization of coal has been reported globally, substantial research on spectroscopic characterization is still scarce. Chemical leaching of coal using acid and alkali solutions helps to reduce ash forming minerals to a large extent. These processes, either alone or followed by a physical technique, are extensively used for the production of clean coal. The general approach followed to upgrade low rank coal has involved leaching under a variety of conditions.

The approach of bioleaching with microbes in combination with dilute acids has been studied worldwide and is extremely effective when the concentration of minerals is very low. It is the extraction of metals from their ores through the use of living microorganisms, where several species of fungi are used. But the processes have not reached widespread commercialization largely due to two reasons. In this scenario, a combined leaching procedure using strong mineral acids, mild organic acids and microbial treatment was developed for demineralization of low rank sub-bituminous coal and the results are summarized.

2. Materials and Methods

Demineralization of coal prior to FT-IR characterization is carried out on well powdered sample. Successive leaching with mineral acid, organic acid, treatment with carboxylic acid and various filamentous fungi are also carried out. The scheme of leaching (Figure 1) is depicted below [6] -[13] .

Demineralization was carried out using hydrofluoric acid. It was modified to include dil. HNO3 as the first reagent followed by HF in different concentrations. In the initial stage, 50 g of coal sample was mixed with 100 ml dil. HNO3 (5%) solution in a 500 ml teflon beaker and stirred for an hour at 30˚C. In the next stage of leaching, 10 g of filtrate was further treated with 100 ml concentrated HF (10% and 40%) for one hour. As an alternative approach, 50 g of sample was washed with 100 ml, 0.1 N EDTA for 24 h followed by leaching in acetic acid column (2 N) over a period of 1 h and 2 h respectively. The resulting samples were recovered by filtration and cleaned repeatedly using de-ionized water. The dried samples were tested for ultimate analysis and subjected to spectroscopic characterizations.

Figure 1. Scheme of leaching.

Bituminous coal was air-dried and ground to the particle size <75 µm, of which 50 g was treated, employing carboxylic acids like gluconic acid (50%), oxalic acid (10%), EDTA, acetic acid and citric acid (10%) separately in a 500 ml teflon beaker for 24 h at room temperature (27˚C). The sample was recovered from the respective organic acid solution by filtration using a poly-propylene funnel.

About 10 g selected coal samples were dried, ground to a particular size and inoculated into 200 ml modified Czepek Dox medium with low sucrose. Cultures of A. niger, A. flavus and Penicillium spp were grown on potato dextrose agar medium till sporulation. The spores were inoculated in modified Czepek Dox medium containing coal sample as four different sets A. niger (AS), A. flavus (FL), Penicillium spp (PE) and mixed culture of A. niger and Penicillium spp (APE). The FT-IR spectra of samples were recorded over the range, 4000 - 500 cm−1 on a Shimadzu FT-IR spectrometer using KBr pellet technique.

3. Results and Discussion

3.1. Vibrational Spectroscopic Analysis of Successively Leached Coal

The FT-IR spectra of coal solubilized with different reagents are recorded in Figure 2. Samples leached with acetic acid and EDTA (GEA1-GEA3-1 hr to 3 hrs) showed sharp bands at 540 and 1030 cm−1, which are assigned to the vibration of Si-O-Si in quartz and kaolinite [1] -[4] . The peaks at 2920 and 2850 cm−1 are due to the existence of aliphatic groups in coal samples and that at 1600 cm−1 corresponds to aromatic C=C structure. The symmetric deformation associated with -CH3 group is observed at 1398 cm−1. The complex band (900 - 700 cm−1) indicates the aromatic structures within the coal. The spike at 670 cm−1 is ascribed to C-S band. The vibrational frequencies of oxygen in C-O-R structure spread from 1149 to 1016 cm−1. The presence of illite and kaolinite, due to poor demineralization by organic acid, is confirmed. The 1350 - 1000 cm−1 band is complex, because of the contribution of different functional groups and mineral matter in the acetic acid leached samples. Several functional and mineral groups are found to be absent, which reveals that, HF treatment has the potential to demineralize coal successfully [6] -[9] .

It is therefore conjectured that, the two-stage leaching using HNO3 followed by HF remarkably reduced the ash content as well as the minerals including Al, Si and Ca. The results showed lack of oxidation in the organic structure of coal during the process. The solubilization of samples with buffered EDTA could not eliminate the minerals in coal.

Figure 2. FT-IR spectra of demineralized coal samples (GEA1-GEA3-Acetic acid and EDTA leached samples for 1 hr to 3 hr. GNF1-GNF3-Nitric acid and HF leached coal samples 10% to 30%).

3.2. Vibrational Mode Analysis of Carboxylic Acid Leached Coal

The vibrational spectroscopy is a pre-requisite for the analysis of functional groups in a complex material, which triggered the identification of prominent bands in virgin and leached bituminous coal (and Figure 3). Intense bands observed at 540 cm−1, 3618 cm−1 and 3696 cm−1 are attributed to clay, silicate, kalonite and illite minerals [5] -[8]. The presence of a broad and strong band observed in all the samples at 3640 cm−1 could be assigned to hydroxyl stretching vibrations. The sharp intense bands (2920 and 2850 cm−1) represent the valency oscillations of -CH3 and -CH2 aliphatic groups. In very low rank coals, the intensity of peak at 2920 cm−1 is found to be very small, because a part of the aliphatic -CH hydrogen is substituted by hydroxyl groups. A great abundance of C=O and C-O-R is revealed by the presence of high intensity peaks in 1800 - 1000 cm−1 region [10] -[15] . A weak absorption in the spectra is noted for the samples leached with organic acids, similar to the observations of Supaluknari et al. [15] in the case of oxygen rich Australian brown coals. Manoj [5] -[10] have reported an elaborate discussion on the assignment of 1600 cm−1 band of carbons. The band associated with low rank coals and chars has been assigned to aromatic ring stretch of small, discrete entities. In the present investigation, this band became distinct with organic acid leaching, indicating an increase in carbon content. The band at 1375 cm−1 is normally present in low rank coals, whose intensity decreases in the solubilized product and is due to the stretching modes of methylene and methyl groups. The weak broad band observed at 1030 cm−1 is attributed to C-O stretching of phenolic groups and trace amount of silicate minerals associated with the samples.

The silicate and kaolinite bands showed a systematic lowering on EDTA and carboxylic acid treatment. The leaching procedure has driven a partial decrease in the intensity of mineral bands. Thus the investigations by FTIR analysis offered a crystal clear manifestation of the samples.

3.3. Spectral Analysis Bio-Solubilized Coal

In the present work, FT-IR spectroscopy has been used to obtain information on changes in the molecular structure of coal. The FT-IR spectra of bio-solubilized coal samples are illustrated in Figure 4. Sharp intense bands were observed at 2920 and 2850 cm−1 for all the samples, which could be due to the valency oscillations of -CH3 and -CH2 aliphatic groups. This might also arise from the stretching vibrations of -CHO group as reported by Basaran et al. [2] . Of these, the band at 2850 cm−1 was assigned to methoxy groups. The sharpness of bands in the selected samples indicated the probable age of coal belonging to tertiary formations. In very low rank coals, the intensity of 2920 cm−1 band will be very small because, the proportion of aliphatic -CH3 hydrogen is substi-

Figure 3. FT-IR spectra of chemical leached samples (KX-Virgin coal, KC-Citric acid, KGl-Gluconic acid, KA-Acetic acid, KE-EDTA, KO-Oxalic acid leached coal samples respectively).

Figure 4. FT-IR spectra of bioleached samples (AS-A. niger, PE-Penicillium spp, APEMixed culture, FL-A. flavus leached coal samples).

tuted by hydroxyl groups [8] [12] -[14] .

The sub-bituminous coals showed medium absorption, as they are moderately ranked. The medium intensity band at 1460 cm−1 is due to the scissoring (bending) vibration of -CH2 group next to the carbonyl group. Its first overtone coupled with the absorption due to aliphatic -CH3 vibrations appear as a strong band at 2924 cm−1. Sub-bituminous coal samples have large absorptivities for different aliphatic-CH bonds, the highest being most likely for those in long chain methylene structure [6] .

The aromatic C=C stretching vibrations (1635 - 1600 cm−1) caused strong absorption, indicating more carbon content. This is possible by the reduction of oxygen via transformation of C=O to CH2 or due to decarboxylation of the matrix, which in turn improved the quality of carbon, hydrogen and hence the calorific value. A. flavus (FL) and mixed culture leached coal exhibited maximum intensity of absorption at 1600 cm−1, while minimum in the case of A. niger (AS) and Penicillium spp (PE). On comparing the spectrum, a remarkable absorption near 1440 cm−1 was observed for all samples, marking the presence of methyl groups. The bands at 1541 and 1442 cm−1 are normally present in immature coals with more lignin content. These bands were diminished from strong absorption to weak, in the spectra of solubilized product of AS and PE, revealing the effectiveness of Penicillium spp and A. niger insolubilizing the lignin. The band at 1375 cm−1 was ascribed to the absorption of methyl symmetric bending vibrations in tertiary butyl groups, which is normally present in low rank coals [7] -[10] [13] -[15] . The intensity of hydroxyl stretching vibrations (1410 - 1310 cm−1) was found to be decreased. The intensity of aliphatic stretching -CH stretching (2980 - 2845 cm−1), asymmetric -CH2 and -CH3 bending (1485 - 1400 cm−1) vibrations also decreased moderately, when treated with Penicillium spp (PE) and A. niger (AS). The silicate bands at 1010, 1030 and 1090 cm−1 exhibited minimum absorption after bio-leaching. The FT-IR analysis confirmed the modification of functional groups of coal on bio-solubilization. Many characteristic functional groups of low rank coals probably decreased the resistance towards the activity of microbial organisms. The fungi is proved to be effective for low rank coals, which contained phenolic, carboxylic, carbonylitic functional groups, methylene, oxygen and sulphur bridges, exchangeable cations and non-condensed aromatic rings. From the experimental trials, it was proved that, Penicillium spp and A. niger were more effective in solubilizing silicate minerals than A. flavus.

4. Conclusion

It is conjectured that, the two-stage leaching using HNO3 followed by HF remarkably reduced the ash content as well as the minerals including Al, Si and Ca. The results showed lack of oxidation in the organic structure of coal during the process. The solubilization of samples with buffered EDTA could not eliminate the minerals in coal. The silicate and kaolinite bands showed a systematic lowering on EDTA and carboxylic acid treatment. The leaching procedure has driven a partial decrease in the intensity of mineral bands. Thus the investigations by FT-IR analysis offered a crystal clear manifestation of the samples. The fungal leaching was most beneficial for aromatic molecules with different degrees of substitution. The intensity of bands due to carbonyl groups was increased, when treated with fungi, whereas that due to oxygen functional groups showed a reverse trend. The mineral bands due to silicates also decreased in intensity, on post treatment with fungal culture.

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