A Method for Preparation of Desulfurizing Biomass and Bioupgraders from Crude Oil

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Austin J Biotechnol Bioeng. 2023; 10(1): 1122.

A Method for Preparation of Desulfurizing Biomass and Bioupgraders from Crude Oil

Wisam Mohammed Kareem Al-Khazaali1,2; Seyed Ahmad Ataei2*

¹Chemical Engineering Sec., Designs Dept., Projects Div., Misan Oil Company, Misan, Iraq

²Department of Chemical Engineering, Faculty of Engineering, Shahid Bahonar University of Kerman, Kerman, Iran

*Corresponding author: Seyed Ahmad Ataei Department of Chemical Engineering, Faculty of Engineering, Shahid Bahonar University of Kerman, Kerman, Iran. Email: [email protected]

Received: October 18, 2023 Accepted: November 15, 2023 Published: November 22, 2023

Abstract

Emissions from human activities contribute to air pollution, global warming, and environmental degradation. These effects can harm human health and ecosystems, underscoring the importance of sustainable practices to mitigate the impact of emissions on the environment. By the time on the first exploration of reservoirs and first design contracts dates of refineries, there are many challenges appeared on the health, safety, and environment by conduction of the oil such as the higher contents of sulfur, nitrogen, oxygen, halogen, metals, and aromatics. There are many side effects on the human health starting from the simple to the malignant diseases such as cancer. Also, the safety of equipment and catalysts are affected by the presence of high content of these impurities in oils by many phenomena such as corrosion, erosion, and poisoning. In this study, microorganisms’ colony has been isolated from Amara crude oil by using 9k medium (ATCC 2436). It was found that this colony has the ability to make Biodesulfurization (BDS) of crude oil from 4.4 to 3.845 %. Also, it was found that this isolated colony upgraded the oil in improvement API-density.

Keywords: Biodesulfurization; Biodegradation; Isolation; 9k medium; Acidithiobacillus ferroxidanse; Thioxidans

Introduction

Fossil fuel is an important source of energy or power in various fields in life and industry. Before applying it in use, it must be on specification of some related standards to avoid risks on HSE. Then, sulfur compounds are one of these constraints to be treated. Fossil fuels take many forms, ranging through crude oil, petroleum fractions, coal, tar sands, and shale oil. In order to compete the sources of clean energy, fossil fuels must care HSE, quantity assurance and quality control regulations (QQHSSE). Emissions of sulfur has resulted in related health issues due to the poor safety of corrosion leading to its leakage to the environment, like: heart diseases, asthma, and respiratory illnesses [1]. Acute toxicity by H2S, which has caused many deaths in the workplace and in areas of natural accumulation. Also, loss of consciousness by H2S, paralysis, and even death, and disorders of the nervous system by H2S exposure, and in cardiovascular, gastrointestinal, and ocular disorders [2].

Emission of SOx leading to serious environmental issues after combustion or due to the poor safety of corrosion, such as acid rain, a deposition of acids that is harmful to agriculture, wildlife, and human health and severe air pollution [1]. However, the combustion of fossil fuels releases many hazardous components such as SOx , NOx, CO2 [3]. Emissions of H2S leading to air pollution [4].

Therefore, EPA limited the total content of sulfur to 15 ppm in diesel and 30 ppm in gasoline. While EU limited to 50 ppm for both of them [4,5].

Sulfur compounds in oils formulate a challenge towards the human being locally and globally, whereas its oxides may reach 2.28 ppm in Baghdad [6]. Whereas, the total content of sulfur in Iraq exceeded all the percentages of other countries as shown in Figure 1 [7].

Figure 1: Total content of sulfur and API-density of various countries lower than Iraq.

    

    
    

    

    Figure 1: Total content of sulfur and API-density of various countries lower than Iraq.

These are many methods for treating that. BDS is a process that is based around bacterial potential. In this process, bacteria remove organosulfur from oil fractions without degrading the carbon skeleton of the compounds. BDS operates at ambient temperature and pressure with high selectivity, resulting in decreased energy costs, low emission and no generation of undesirable side-products. For assessing the potential of BDS as a biorefining process, pilot plants have been operated [8]. BDS is one of the modern biotechnology sciences which deal with the solving the contaminants of oils such as crude oil, its derivatives, and coal too. The content of sulfur causes various problems of health, safety, and environments, then it decrease the products quality and sustainability. In this treatment, it is necessary to test the concentration of sulfur and other biological indicators before, after, and through the treatment. The following sections show these important tests.

To achieve that limitations of quality, there are many methods such as ODS and HDS. In this study, BDS is presented and evaluated. While to achieve the limitations of pollution of soil, there are some methods such as biodegradation.

The isolates of microorganisms from crude oil were identified as Acidithiobacillus strains as provided in Figure 2, Figure 3, Table 1. Also these strains gave biodesulfurization and biodegradation pathways as shown in Figure 4.

Table 1: Preferential of thiobacillus strains on the 9k medium and similar [11].





  

    
Microorganism

    
Name

    
Microorganism codes

    
Medium codes

    
pH

    
Remarks

  

  

    
Acidithiobacillus ferroxidans

    
Acidithiobacillus ferroxidans

    
PTCC    1646

      DSM 583

    
PTCC    105

    
1.4

    
Same 9k

  

  

    
Acidithiobacillus ferroxidans

    
PTCC    1647

    
PTCC    106

      PTCC    132

    
2-2.3

    
9k    medium

  

  

    
Acidithiobacillus ferroxidans

    
PTCC    1746

      ATCC    23270

      DSM    14882

    
PTCC    105

      PTCC    132

    
1.4

      1.8

    
Same 9k

  

  

    
Acidithiobacillus

      thiooxidans

    
Thiobacillus thioparus

    
PTCC    1668

      DSM    5368

    
PTCC    158

    
6.6

    
Same    constitutes of 9k medium

  

  

    
Acidithiobacillus

      Thiooxidans

    
PTCC    1692

      ATCC    8085

      IFO    12544

      NBRC    12544

      NCIMB    9112

    
PTCC    119

    
4.2

    
Same    positive roots and different negative bases.

  

  

    
Acidithiobacillus

      Thiooxidans

    
PTCC    1717

      DSM    9463

    
PTCC    123

    
3.5

    
Same

  










Table 1: Preferential of thiobacillus strains on the 9k medium and similar [11].

Figure 2: Proposed morhology of isolated microorganisms. (a) Acidithiobacillus ferrooxidans magnification 30,000 times. [Henry Lutz Ehrlich, Geomicrobiology, 2nd edition, (New York: Marcel Dekker, 1990)] (b) Acidithiobacillus thioxidans isolated by 9k medium [9].

    

    
    

    

    Figure 2: Proposed morhology of isolated microorganisms. (a) Acidithiobacillus ferrooxidans magnification 30,000 times. [Henry Lutz Ehrlich, Geomicrobiology, 2nd edition, (New York: Marcel Dekker, 1990)] (b) Acidithiobacillus thioxidans isolated by 9k medium [9].

Figure 3: Alignment of the nucleotide sequences of the coxC genes from named AF1,AF3 and AFc strains [10].

    

    
    

    

    Figure 3: Alignment of the nucleotide sequences of the coxC genes from named AF1,AF3 and AFc strains [10].

Figure 4: Typical metabolism pathways [Mohebali]. (a) The 4S pathway (black thick arrows) and the extended 4S pathway (white arrow). (b) The C-C cleavage pathway that releases sulfur (dotted thin arrows), (3) the sulfur-oxidation pathway (black thin arrow) and (4) the Kodama pathway (dotted thick arrows).

    

    
    

    

    Figure 4: Typical metabolism pathways [Mohebali]. (a) The 4S pathway (black thick arrows) and the extended 4S pathway (white arrow). (b) The C-C cleavage pathway that releases sulfur (dotted thin arrows), (3) the sulfur-oxidation pathway (black thin arrow) and (4) the Kodama pathway (dotted thick arrows).

Materials and Methods

A sample of crude oil was brought from storage tanks in Amara Oilfield from Iraq and iron concentrate from mountains of Kerman in Iran. These samples should not be sterilized in order not affecting the microorganisms in it. A 5-litre was withdrawn to cover all the experiments. The culture 9k medium (ATCC 2436 or PTCC 106) was used in the isolation. This medium is composed of FeSO4.7H2O 45g, glucose 10g, (NH4)2SO4 3g, K2HPO4 0.75g, MgSO4.7H2O 0.5, KCl 0.1g, CaNO3 0.01g. This medium is prepared separately with FeSO4.7H2O in order to avoid the sedimentation of it after the sterilization. pH of this solution must be adjusted to 5.5 with H2SO4 then autoclaved at 120°C and pressure 15 psi for 20 minutes. While the FeSO4.7H2O solutions is sterilized by using microfilter (0.4 μm) and adjusted pH 1.4 by H2SO4. After cooling, they were mixed and kept in a dark place.

The emulsifier or surfactant Tween 20 was used in order to make dispersion of oil phase in the aqueous phase. In this study, the 9k medium was used for each of isolation culture, growth, and incubation XRF analyzer was used for measurement of the total content of sulfur in the crude oil. The sulfur measurement was tested by Misan Oil Company and Asfahan University. Also, some decanters was used in the primary separation. The centrifuge was used for deeply purification of separation as a secondary stage. Finally, a reverse-emulsifier was used in the tertiary separation such as n-heptane.

IP 77 and STM D473 have been used to ensure the crude oil is free of salts and sediments respectively. This is important for the selectivity of significant microorganisms comprised with salts and constitutes of apllied medium which is 9k medium. Also, ASTM D4006 was used to make sure of oil is not wet. ASTM D1298 and ASTM D5002 had been applied to measure the density. All these tests have been reported from Misan Oil Company.

The operation conditions must be carefully selected to study the upgrade and improvement of heavy crude oil such as the temperature, speed of rotation, pH, oil water ratio (OWR), and the surfactant dose, and the time of isolation, cultivation, and incubation. the isolation was done by using a solidified 9k medium with agar 1.5 %. The operation conditions for the isolation were temperature 30°C and time 3 day. The initial conditions of incubation were speed of rotation 150 rpm, temperature 35°C, OWR 5%, surfactant dose 1% of oil volume, time 3 day.

Results

The colony was isolated firstly by using the solidified 9k medium in a petridish. Then inoculated in Erleynmeyer for decreasing the growth in the incubator. The strains was Yellow Form Colony (YFC). As shown in Figure 5.

Figure 5: Bio-mixture of isolated colony supplemented by 9k medium. (a) Isolation of colony from oil and concentrate with gell medium solidified by agar 1.5 %. (b) Inoculation and adaptation by some dropes of crude oil as sole source of sulfur. (c) Incubation of crude oil assisted by surfactant.

    

    
    

    

    Figure 5: Bio-mixture of isolated colony supplemented by 9k medium. (a) Isolation of colony from oil and concentrate with gell medium solidified by agar 1.5 %. (b) Inoculation and adaptation by some dropes of crude oil as sole source of sulfur. (c) Incubation of crude oil assisted by surfactant.

The Metabolism Ability

The incubation biomixture was made by using Erlynmeyer 250 ml as shown in Figure 5C. The metabolism reaction ability was found according to the change in measurement of total content of sulfur, salts, pH, electric conductivity, and density. Based on the XRF analysis of the treated and untreated crude oil, it was found the capability of bio-upgrade and bio-improvement for the applied microorganisms on the crude oil from Amara oilfield. It was that the isolated colony from Amara Oilfield is able to make the desulfurization of oil. Table 2 shows the results of before and after the incubation of crude oil by the colony.

Table 2: Effect of incubation on the physical and chemical properties.





  

    
 

    
Initial

    
Final

    
Unit

  

  

    
Total content of sulfur

    
4.4

    
3.845

    
%

  

  

    
Total content of salts

    
49.36

    
40

    
g/l

  

  

    
pH

    
2

    
1.75

    
-

  

  

    
Electric conductivity

    
155

    
88

    
μS/cm

  

  

    
API-Density

    
23.6

    
22.5

    
API

  










Table 2: Effect of incubation on the physical and chemical properties.

Discussion

This isolate have the ability of metabolism bioreaction of crude oil because the tendency of investment of organosulfur compounds as the sole source of sulfur [12,13]. This colony could contain some bacteria such as multi strains of Acidithioballus which have the ability to desulfurize or defrade the crude oil and its derivative [14,15]. But mainly, 9k medium encourages the growth of the strains of thiobacillus [16,17] in addition to preferential tendency to medium PTCC 105 [11,18]. It was founded that 9k medium can extract four stains of Acidithiobacillus ferrooxidans which have been identified by phenotypicand 16S rDNA sequence analyses as shown in Figure 3. These isolates could make use of Fe2+, S, or pyrite as a sole source of energy in different activities in various preferences of pH, temperature, resistance to chloride (KCl) and heavy metal ions, and oxidation rates of Fe2+, S and pyrite [10]. In general, 9k medium and its similar give the Acidithiobacillus strains as mentioned by ATCC [19] and shown by PTCC in Table 2.

The pH value of 9k medium gives a hint that the predominant microorganisms in the colony are Acidithiobacillus ferroxidans strains, because the Acidithiobacillus thiooxidans strains prefer higher pH values, i.e., lower acidity. Therefore, Acidithiobacillus ferroxidans ATCC 23270 is applied in bioleaching or biomining due to the acidity of microorganism and Fe ions in 9k medium [20]. The lower efficiency can explain the presence of Biodegradation (BDG) microorganism as in the case Acidithiobacillus strains on some organosulfur compounds [21]. Also, the lower efficiency can be attributed to the competence among various biological strains in colony and chemical species in medium [22]. Due to the limited rate of BDS in addition to the chemical methods such as HDS, then sometimes deep desulfurization is studied and applied such as the physical methods like extraction to improve the quality of fuels [23], and deep biodegradation for the environmental improvement. These different pathways are shown in Figure 3.

Conclusions

It was found that the heavy crude oil can produce bacteria strains which have the ability of BDS. This isolate colony was able on bioupgrade in addition to the biodesulfurization. For more accurately, this colony can be purifies to get pure cultures such as Acidithiobacillus ferroxidans. This can give clearer philosophy of each microorganisms functions as BDS or BDG because the competence among the various microorganisms on the sources of sulfur compounds in crude oil. Whereas, in the case of pure culture, the efficiency of desulfurization can be increased significantly.

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Citation: Al-Khazaali WMK, Ataei SA. A Method for Preparation of Desulfurizing Biomass and Bioupgraders from Crude Oil. Austin J Biotechnol Bioeng. 2023; 10(1): 1122.