High Molecular Weight Hydrocarbons Research Articles

Optimization and Techno-Economic analysis of catalytic gasification of wheat straw biomass using ASPEN PLUS model

Biomass gasification efficiently produces heat, electricity, and power. However, removing harmful contaminants from raw syngas is crucial. Tar production is a challenge due to blockage, plugging, and corrosion. Tar steam reforming (TSR) is the most promising technique, converting high molecular weight hydrocarbons into CO, CO2, H2, and CH4. In this study, a model of biomass gasification using wheat straw as biomass feedstock has been developed using Aspen Plus. The gasification flow sheet encompasses gasification, catalytic filter candle, gas cleaning, impurity removal reactor, separator, and subsequent sorbent reactors. Ni-based catalysts with Ni ratios (5%, 10%, and 15%) are used to simulate TSR reactions. Results show that the 15% Ni-Co-Al2O3 catalyst outperforms the 10% and 5% Ni-Co-Al2O3 catalysts. This study explores the impact of temperature, catalyst loadings, and steam-to-carbon (S/C) ratios on toluene conversion and hydrogen yield in catalytic steam reforming, along with temperature, steam-to-biomass ratios, and equivalence ratio on syngas fraction in gasification. It includes a techno-economic analysis of wheat straw gasification to improve syngas energy through efficient tar conversion.

The Role of Zeolite (Microporous Crystalline Aluminosilicates) In Catalytic Pyrolysis of Waste High- and Low-Density Polyethylene Bags for Production of Fuel and Chemicals: A Review

This review provides a state-of-the-art summary of the role which zeolite plays as a catalyst via pyrolysis as a way of recovering fuels and chemicals from waste high and or low density polyethylene bags. It also highlighted the two types of zeolite (natural or synthetic) which are used as a two-stage pyrolysis−catalysis in giving a free waxing product to pure fuel and chemicals which can be subjected to further analyzing and or upgrading. As yield of oil/wax decreased with the addition of a zeolite as catalyst from 44 and 51 wt.%, (depending on the waste high density polyethylene “HDPE” or low density polyethylene bags “LDPE” and other factors). However, the composition of the pyrolysis−catalysis oils significantly increased in aromatic hydrocarbon content accordingly. In addition, the composition of the oils shifted from high molecular weight hydrocarbons (C16+) to fuel range hydrocarbons (C5−C15), with a high content of single-ring aromatic hydrocarbons such as benzene, toluene, ethylbenzene, xylenes, and styrene. This process shows great potential for production of fuels or chemicals, and also addresses the urgent issue of waste HDPE and or LDPE disposal.

Toward sustainable production of N-containing products via nonthermal plasma-enhanced conversion of natural gas resources

Nonthermal plasmas can directly activate and cleave the strong chemical bonds in molecular nitrogen and methane to facilitate the transformation of these inherently stable molecules through the application of electrical energy. Here, we report a low temperature, atmospheric pressure, nonthermal plasma for the “one-pot” synthesis of olefins, alkynes, higher molecular weight hydrocarbons, ammonia, and nitrogen-containing liquids from a representative shale gas feed enriched with nitrogen. We reproducibly observe a wide range of valuable and synthetically challenging gas-phase and liquid-phase products containing C–N, C–C, and N–H bonding by controlling the N2 concentration in the inlet feed stream. In nitrogen-lean regimes, hydrocarbon products dominate (e.g., ethylene, acetylene, etc.), while nitrogen-rich regimes promote incorporation of nitrogen into the products, leading to the formation of ammonia and liquid products containing a variety of functionalities (e.g., nitriles, amines, heterocycles). High resolution electrospray ionization mass spectrometry was used to measure molecular weights and identify the chemical formulas of the liquid products. Van Krevelen diagrams were created and showed many products with compositions around H/C= 2 and N/C= 0.5, indicating the potential importance of intermediate species with these ratios for liquid formation (e.g., CH3CN + H).

Catalytic Cracking of 1,3,5‐Triisopropylbenzene and Low‐Density Polyethylene over Hierarchical Y Zeolites and Al‐SBA‐15

AbstractCatalytic cracking of high molecular weight hydrocarbons underpins the production of fossil fuels from petroleum vapour and the recycling of polyolefin waste plastic. However, thermal cracking over conventional microporous solid acids is hindered by poor mass‐transport. Here we explore the performance of hierarchical H−Y zeolites and Al‐SBA‐15 for the catalytic cracking of 1,3,5‐triisopropylbenzene (1,3,5‐TIPB) and low‐density polyethylene (LDPE) in a continuous fixed‐bed flow reactor. Dealumination by acid washing was used to create hierarchical mesoporosity in H−Y zeolite and modify the solid acidity. Physicochemical properties were studied by X‐ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), gas adsorption, in‐situ Fourier transform infrared (FTIR), ex‐situ pyridine DRIFT, 29Si and 27Al nuclear magnetic resonance (NMR), and 1H relaxation and pulsed field gradient (PFG) NMR diffusion studies. Despite weakening acidity, the introduction of hierarchical porosity promotes deep cracking of both feedstocks; HNO3 dealuminated H−Y produces five times more cumene and benzene from 1,3‐5‐TIPB, and 33 % more benzene and xylenes from LDPE, than the parent H−Y.

Ignition and Combustion of Synthetic High Molecular Weight Hydrocarbons in High-Enthalpy Air Flow

Ignition and Combustion of Synthetic High Molecular Weight Hydrocarbons in High-Enthalpy Air Flow

Isolation, identification, and screening of biosurfactant-producing and hydrocarbon-degrading bacteria from oil and gas industrial waste

Qatar is one of the biggest oil and gas producers in the world, coupled with it is challenging environmental conditions (high average temperature: >40 °C, low annual rainfall: 46.71 mm, and high annual evaporation rate: 2200 mm) harbors diverse microbial communities that are novel and robust, with the potential to biodegrade hydrocarbons. In this study, we collected hydrocarbon contaminated sludge, wastewater and soil samples from oil and gas industries in Qatar. Twenty-six bacterial strains were isolated in the laboratory from these samples using high saline conditions and crude oil as the sole carbon source. A total of 15 different bacterial genera were identified in our study that have not been widely reported in the literature or studied for their usage in the biodegradation of hydrocarbons. Interestingly, some of the bacteria that were identified belonged to the same genus however, demonstrated variable growth rates and biosurfactant production. This indicates the possibility of niche specialization and specific evolution to acquire competitive traits for better survival. The most potent strain EXS14, identified as Marinobacter sp., showed the highest growth rate in the oil-containing medium as well as the highest biosurfactant production. When this strain was further tested for biodegradation of hydrocarbons, the results showed that it was able to degrade 90 to 100% of low and medium molecular weight hydrocarbons and 60 to 80% of high molecular weight (C35 to C50) hydrocarbons. This study offers many promising leads for future studies of microbial species and their application for the treatment of hydrocarbon contaminated wastewater and soil in the region and in other areas with similar environmental conditions.

Bioremediation: Review on oil spill management using oil eating microorganisms, and spill effects on marine and terrestrial environment

With never ending increase in usage and demand of petroleum products worldwide chances of its spill also increase. Oil spills directly affect marine as well as terrestrial ecosystem, as petroleum product became source of water pollution. Marine shorelines serve as home to variety of wildlife oil spills thus destroying habitat of different animals by polluting coastline. Fishes and birds being the main victims. Different physical and chemical methods are used to manage oil spills. However bioremediation is considered as best procedure to manage oil spills around the world. Bioremediation uses the oil loving microbes (lyophilic) to cope oil spills, microbes are cable of destroying complex chemical compounds, some bacteria consume hydrocarbon as their ultimate energy and carbon source. Although process is considered as highly effective the rate at which degradation occur is very slow to prevent oil effecting shore and marine ecosystem, generally due to limitation of availability of nutrients which are generally nitrogen and phosphorous. Two type of methods are generally involved in bioremediation, these include bio augmentation and bio stimulation. In bio augmentation biodegradable bacteria are added to existing population at effected site while in bio stimulation, is addition of nutrients to make process more effective and efficient. Latest technology introduce use of nanoparticles in bioremediation. Along with bacteria some microalgae are under consideration for effective bioremediation. Challenges involve in biodegradation include slow bioremediation of polycyclic hydrocarbons of high molecular weight, i.e. asphaltenes can be difficult to deal .While failure of some techniques which are successful in laboratory at effected site is another problem .The review focus on oil spill effects, new trends in bioremediation developing technique and microbial bioremediation agents.

Lanolin.

Lanolin is a complex mixture of high molecular weight esters, aliphatic alcohols, sterols, fatty acids, and hydrocarbons that has been widely used for centuries for its emollient properties. The purification of crude lanolin into lanolin wax and the processing of this wax into various derivatives began in 1882 and continue to this day with newer highly purified anhydrous lanolins. Controversy as to lanolin's allergenicity began in the 1920s and remains an issue. The most appropriate patch test preparation(s) for detecting allergy remain disputed. Detection of lanolin-induced contact dermatitis in diseased skin by patch testing on normal skin may lead to false negative results. Patients with a positive patch test to lanolin may tolerate use of lanolin on normal skin. Although lanolin is a weak sensitizer and the frequency of contact allergy to it in the European population reportedly is 0.4%, there are high-risk concomitant conditions: stasis dermatitis, leg ulcers, perianal/genital dermatitis, and atopic dermatitis (AD). Children and the elderly are also at greater risk of developing contact allergy to lanolin, partly because of comorbidities (AD and stasis dermatitis/leg ulcers, respectively). Finally, in the United States, non-Hispanic white patients are more likely than their non-Hispanic black counterparts to be lanolin allergic.

Fisher–Tropsch Synthesis for Conversion of Methane into Liquid Hydrocarbons through Gas-to-Liquids (GTL) Process: A Review

The interest in Gas-to-Liquid technology (GTL) is growing worldwide because it involves a two-step indirect conversion of natural gas to higher hydrocarbons ranging from Liquefied Petroleum Gas (LPG) to paraffin wax. GTL makes it possible to obtain clean diesel, naphtha, lubes, olefins, and other industrially important organics from natural gas. This article is a brief review discussing the state-of-the-art of GTL, including the basics of syngas manufacturing as a source for Fischer-Tropsch synthesis (FTS), hydrocarbons synthesis (Fischer-Tropsch process), and product upgrading. Each one is analyzed, and the main characteristics of traditional and catalysts technologies are presented. For syngas generation, steam methane reforming, partial oxidation, two-step reforming, and autothermal reforming of methane are discussed. For Fischer–Tropsch, we highlight the role of catalysis and selectivity to high molecular weight hydrocarbons. Also, new reactors technologies, such as microreactors, are presented. The GTL technology still faces several challenges; the biggest is obtaining the right H2:CO ratio when using a low steam-to-carbon ratio. Despite the great understanding of the carbon formation mechanism, little has been made in developing newer catalysts. Since 60–70% of a GTL plant cost is for syngas production, it needs more attention, particularly for developing the catalytic partial oxidation process (CPO), given that modern CPO processes using a ceramic membrane reactor reduce the plant’s capital cost. Improving the membrane’s mechanical, thermal, and chemical stability can commercialize the process. Catalytic challenges accompanying the FTS need attention to enhance the selectivity to produce high-octane gasoline, lower the production cost, develop new reactor systems, and enhance the selectivity to produce high molecular weight hydrocarbons. Catalytically, more attention should be given to the generation of a convenient catalyst layer and the coating process for a given configuration.

Biosurfactant Production from the Biodegradation of n-Paraffins, Isoprenoids and Aromatic Hydrocarbons from Crude Petroleum by Yarrowia lipolytica IMUFRJ 50682

Yarrowia lipolytica is a unique, strictly aerobic yeast with the ability to degrade efficiently hydrophobic substrates. In the present work, we evaluated the degrading potential of Yarrowia lipolytica IMUFRJ 50682, isolated from tropical estuarine water in Rio de Janeiro (Brazil), and the possible biomolecules produced during this process. To investigate which crude oil compounds are degraded by Y. lipolytica IMUFRJ 50682, this microorganism was grown in a medium containing Marlim petroleum (19 °API, American Petroleum Institute gravity) at 28 °C and 160 rpm for 5 days. The residual petroleum was submitted to gas chromatograph-mass spectrometric analysis (GC-MS). The chromatographic fingerprints of the residual petroleum were compared with the abiotic control test incubated in the same conditions. Y. lipolytica assimilates high molecular weight hydrocarbons, such as n-alkanes (C11-C19), isoprenoids (pristane and phytane), aromatics with two or three aromatics rings (naphthalene, methylnaphthalenes, dimethylnaphthalenes, trimethylnaphthalenes, phenanthrene, methylphenanthrenes, dimethylphenanthrenes, anthracene). This strain was also capable of consuming more complex hydrocarbons, such as tricyclic terpanes. During this biodegradation, the emulsification index of the culture medium increased significantly, showing that biosurfactant molecules can be produced from this process. Therefore, Y. lipolytica IMUFRJ 50682 showed to be a potential crude oil degrading yeast, which can be used for bioremediation processes and simultaneously produce bioproducts of commercial interest.

Developing an adaptive catalyst for an FCC reactor using a CFD RSM, CFD DPM, and CFD DDPM–EM approach

Cyclone separators, which have an important role in the recovery of catalysts, constituted one of the aims of the study. In the work to be done, the pressure drop occurring during the fcc reaction is also calculated using the Ergun equation and it is aimed to provide the same value in a cyclone separator. In this study, which was presented for the first time in the literature, the best working conditions were determined by simulating the pressure drop in the cyclone separator modeled by using the various catalyst types namely NiMo/ASA–Al2O3, NiMo/p–Al2O3, NiMo/Y–Al2O3, Co-Mo, HZSM-5 zeolite, HY zeolite, pAl2O3, ASA-Al2O3, Y-Al2O3 determined from the literature in the Ergun equation. Among them, NiMo/ASA Al2O3, Co-Mo, HY zeolite, and ASA-Al2O3 were determined as the best catalyst for producing diesel from high oil fractions. Unlike previous studies, the condition that the cyclone separator modeled cleans the catalyst with maximum efficiency also determines the condition that provides low catalyst porosity in the determination of the catalyst type to be determined in diesel production. Due to the accuracy between the calculated and the predicted pressure drop results (about 1,8%), HY zeolite is the best catalyst for cyclone separator geometry. It is widely used to convert high molecular weight hydrocarbon fractions, the high boiling point of petroleum crude oils into olefinic gases, more valuable gasoline, and other products. The purpose of the FCC unit is to increase the refinery conversion and white product yield by converting heavy vacuum gas oil (HVGO) into light hydrocarbons at high temperatures with the aid of fluid catalysis. These two zones (reactor and regenerator) are placed as two different pressure vessels. For these two different systems to work in harmony with each other, unlike in previous studies, the “dense discreet phase-Eularian” approach was used in the modeling of the catalytic unit and the “discreet phase” approach was used in the modeling of the cyclone separator. The values required for both processes to work together have been determined approximately.

Nitrogen dependence of rhamnolipid mediated degradation of petroleum crude oil by indigenous Pseudomonas sp. WD23 in seawater.

Effect of oil spills on living forms demands for safe, ecofriendly and cost-effective methods to repair the damage. Pseudomonads have exceptional tolerance to xenobiotics and can grow at varied environmental conditions. This study aims at biosurfactant mediated degradation of petroleum crude oil by an indigenous Pseudomonas sp. WD23 in sea water. Pseudomonas sp. WD23 degraded 34% of petroleum crude oil (1.0% v/v) on supplementation of yeast extract (0.05g/L) with glucose (1.0g/L) in seawater. The strain produced a biosurfactant which was confirmed as a rhamnolipid (lipid: rhamnose 1:3.35) by FT-IR, LCMS and quantitative analysis. Produced rhamnolipid had low CMC (20.0mg/L), emulsified petroleum oils (75-80%) and had high tolreance to varied conditions of pH, temperature and ionic strength. OFAT studies were performed to analyse the effect of petroleum crude oil, glucose, inoculum, yeast extract, pH, agitation speed and incubation time on degradation by Pseudomonas sp. WD23. Petroleum crude oil and glucose had significant effect on biodegradation, rhamnolipid production and growth, further optimized by central composite design. At optimum conditions of 3.414% v/v PCO and 6.53g/L glucose, maximum degradation of 81.8±0.67% was observed at pH 7.5, 100 RPM, 15.0% v/v inoculum in 28 days, with a 3-fold increase in biodegradation. GCMS analysis revealed degradation (86-100%) of all low and high molecular weight hydrocarbons present in petroleum crude oil. Hence, the strain Pseudomonas sp. WD23 can be effectively developed for management of oil spills in seas and oceans due to its excellent degradation abilities.

Biodegradation of high molecular weight hydrocarbons under saline condition by halotolerant Bacillussubtilis and its mixed cultures with Pseudomonas species

Biodegradation of high-molecular-weight petroleum hydrocarbons in saline conditions appears to be complicated and requires further investigation. This study used heavy crude oil to enrich petroleum-degrading bacteria from oil-contaminated saline soils. Strain HG 01, with 100% sequence similarity to Bacillussubtilis, grew at a wide range of salinities and degraded 55.5 and 77.2% of 500 mg/l pyrene and 500 mg/l tetracosane, respectively, at 5% w/v NaCl. Additionally, a mixed-culture of HG 01 with Pseudomonasputida and Pseudomonasaeruginosa, named TMC, increased the yield of pyrene, and tetracosane degradation by about 20%. Replacing minimal medium with treated seawater (C/N/P adjusted to 100/10/1) enabled TMC to degrade more than 99% of pyrene and tetracosane, but TMC had lesser degradation in untreated seawater than in minimal medium. Also, the degradation kinetics of pyrene and tetracosane were fitted to a first-order model. Compared to B.subtilis, TMC increased pyrene and tetracosane's removal rate constant (K1) from 0.063 and 0.110 per day to 0.123 and 0.246 per day. TMC also increased the maximum specific growth rate of B.subtilis, P.putida, and P.aeruginosa, respectively, 45% higher in pyrene, 24.5% in tetracosane, and 123.4% and 95.4% higher in pyrene and tetracosane.

Integrative description of changes occurring on zebrafish embryos exposed to water-soluble crude oil components and its mixture with a chemical surfactant

The effects of crude oil spills are an ongoing problem for wildlife and human health in both marine and freshwater aquatic environments. Bioassays of model organisms are a convenient way to assess the potential risks of the substances involved in oil spills. Zebrafish embryos (ZFE) are a useful to reach a fast and detailed description of the toxicity of the pollutants, including both the components of the crude oil itself and substances that are commonly used for crude oil spill mitigation (e.g. surfactants). Here, we evaluated the survival rate, as well as histological, morphological, and proteomic changes in ZFE exposed to Water Accumulated Fraction (WAF) of light crude oil and in mixture with Dioctyl Sulfosuccinate Sodium (DOSS, e.g. CEWAF: Chemically Enhanced WAF), a surfactant that is frequently used in chemical dispersant formulations. Furthermore, we compared the hydrocarbon concentration of WAF and CEWAF of the sublethal dilution. In histological, morphological, and gene expression variables, the ZFE exposed to WAF showed less changes than those exposed to CEWAF. Proteomic changes were more dramatic in ZFE exposed to WAF, with important alterations in spliceosomal and ribosomal proteins, as well as proteins related to eye and retinal photoreceptor development and heart function. We also found that the concentration of high molecular weight hydrocarbons in water was slighly higher in presence of DOSS, but the low molecular weight hydrocarbons concentration was higher in WAF. These results provide an important starting point for identifying useful crude-oil exposure biomarkers in fish species.

Fingerprint analysis reveals sources of petroleum hydrocarbons in soils of different geographical oilfields of China and its ecological assessment

The distribution and characteristics of petroleum in three different geographic oilfields in China: Shengli Oilfield (SL), Nanyang Oilfield (NY), and Yanchang Oilfield (YC) were investigated. The average concentration of the total petroleum hydrocarbons (TPHs) conformed to be in the following law: SL Oilfield > NY Oilfield > YC Oilfield. Fingerprint analysis on the petroleum contamination level and source was conducted by the geochemical indices of n-alkanes and PAHs, such as low to high molecular weight (LMW/HMW) hydrocarbons, n-alkanes/pristine or phytane (C17/ Pr, C18/Ph), and ratio of anthracene/ (anthracene + phenanthrene) [Ant/(Ant + Phe)]. Soils adjacent to working well oils indicated new petroleum input with higher ratio of low to high molecular weight (LMW/HMW) hydrocarbons. The oil contamination occurred in the grassland soils might result of rainfall runoff. Petroleum source, petroleum combustion source, and biomass combustion were dominant PAHs origination of soils collected from oil exploitation area, petrochemical-related sites, farmland and grassland, respectively. The suggestive petroleum control strategies were proposed in each oilfield soils. Ecological potential risk of PAHs was assessed according to the toxic equivalent quantity (TEQ) of seven carcinogenic PAHs. The results showed that high, medium, and low ecological risk presented in petro-related area, grassland soils, and farmland soils, respectively. High ecological risk was persistent in abandoned oil well areas over abandoned time of 15 years, and basically stable after 5 years. This study can provide a critical insight to ecological risk management and source control of the petroleum contamination.

Value-Added Pyrolysis of Waste Sourced High Molecular Weight Hydrocarbon Mixtures

In this study, Fischer-Tropsch paraffin mixture, heavy residue of waste polyethylene pyrolysis, shredded and crashed agricultural polyethylene waste and their combinations were pyrolysed both thermally and catalytically in a two-stage reactor system. During the experimental work, yields and compositions of pyrolysis products were studied as function of feedstock composition and catalyst placement. It was found that the average molecular weight of feedstocks and the presence of ZSM-5 catalyst also have significant effects on the product yields and the compositions. Feedstocks with high concentration of Fischer-Tropsch paraffin and real waste polyethylene resulted in deeper fragmentation in both thermal and thermo-catalytic pyrolysis. Due to the deeper fragmentation, they seemed to be suitable feedstocks for the production of C6–C9 and C10–C14 hydrocarbons. Meanwhile, for production of C15–C21 hydrocarbons, the use of a higher concentration of heavy residue of waste polyethylene pyrolysis in the feedstocks is recommended. From the point of view of liquid hydrocarbon and isomer production, the placement of the catalyst into the 1st reactor proved to be more advantageous. When the catalyst was placed into the 2nd reactor, the product formation shifted to the more volatiles, isomers took part in secondary cracking reactions and aromatics formed in higher concentrations.

Kinetic and statistical perspectives on the interactive effects of recalcitrant polyaromatic and sulfur heterocyclic compounds and in-vitro nanobioremediation of oily marine sediment at microcosm level

A halotolerant biosurfactant producer Pseudomonas aeruginosa strain NSH3 (NCBI Gene Bank Accession No. MN149622) was isolated to degrade high concentrations of recalcitrant polyaromatic hydrocarbons (PAHs) and polyaromatic heterocyclic sulfur compounds (PASHs). In biphasic batch bioreactors, the biodegradation and biosurfactant-production activities of NSH3 have been significantly enhanced (p < 0.0001) by its decoration with eco-friendly prepared magnetite nanoparticles (MNPs). On an artificially contaminated sediment microcosm level, regression modeling and statistical analysis based on a 23 full factorial design of experiments were trendily applied to provide insights into the interactive impacts of such pollutants. MNPs-coated NSH3 were also innovatively applied for nanobioremediation (NBR) of in-vitro diesel oil-polluted sediment microcosms. Gravimetric, chromatographic, and microbial respiratory analyses proved the significantly enhanced biodegradation capabilities of MNPs-coated NSH3 (p < 0.001) and the complete mineralization of various recalcitrant diesel oil components. Kinetic analyses showed that the biodegradation of iso- and n-alkanes was best fitted with a second-order kinetic model equation. Nevertheless, PAHs and PASHs in biphasic batch bioreactors and sediment microcosms followed the first-order kinetic model equation. Sustainable NBR overcome the toxicity of low molecular weight hydrocarbons, mass transfer limitation, and steric hindrance of hydrophobic recalcitrant high molecular weight hydrocarbons and alkylated polyaromatic compounds.

Characterization of bacterial community in oil-contaminated soil and its biodegradation efficiency of high molecular weight (>C40) hydrocarbon

In this study, two biosurfactant producing Pseudomonas aeruginosa sp. were isolated from motor oil contaminated soil for crude oil, alkane and PAH degradation studies. Metagenomics analysis identified as proteobacteria phyla was the dominant. Isolated two bacterial species were well grown in mineral salt medium with 1% of crude oil, alkanes (dotriacontane and tetratetracontane) and PAH (pyrene, benzopyrene and anthracene) as sole carbon sources. Total biodegradation efficiency (BE) of strains PP3 and PP4 in Crude oil degradation evaluated by the analysis of gas chromatography and mass spectrometry was 50% and 86% respectively. BE of PP3, PP4 and mixed consortium in alkane biodegradation were 46%, 47% and 36%, respectively. BE of PP3, PP4 and mixed consortium in PAH biodegradation were 22%, 48% and 35%, respectively. Based on the results revealed that strain pp4 was more efficient bacteria to degrade the crude oil, alkane and PAH than pp3. This was due to the higher production of biosurfactant by PP4 than PP3 and also confirmed in the test of emulsification index (E24). FTIR results showed that the produced biosurfactant could partially solubilize the crude oil hydrocarbons, alkanes and PAH and confirmed as glycolipid (rhamnolipid) in nature. Thus, the obtained results from the GCMS showed that all hydrocarbons were utilized by bacteria as carbon source for biosurfactant production and utilize the high molecular weight hydrocarbons. Based on the present study we can suggest that identified potential biosurfactant producing bacteria are used for biodegradation of high molecular weight hydrocarbon (>C40).

Hydrocarbon generation potential, geochemical characteristics, and accumulation contribution of coal-bearing source rocks in the Xihu Sag, East China Sea Shelf Basin

The Xihu Sag is an important petroliferous area in the East China Sea Basin. Petroleum in this sag was generated from coal-bearing source rocks, i.e., coal, carbonaceous mudstone, and mudstone. The lack of detailed studies on the source rocks restricts petroleum exploration. Hydrocarbon generation potential, geochemical characteristics, and relative contribution were assessed using 38 source rock samples and 13 oil/oil sand samples. Results show that source rocks have different hydrocarbon generation potentials. The total organic carbon (TOC), production yield (S1+S2), extractable organic matter (EOM), and total hydrocarbon content suggest that coal has the highest organic matter abundance, followed by carbonaceous mudstone and mudstone. All source rocks are dominated by Type III-II2 kerogen and are, therefore, gas-prone. Biomarker assemblages indicate that the organic matter of coal is mainly derived from terrigenous higher plants with little contribution from phytoplankton, accompanied by strong bacterial modification, which was deposited in an oxidizing depositional environment with a poorly stratified water column. Mudstones, in contrast, have less terrigenous higher plants but higher phytoplankton contributions and were deposited in a more reducing depositional environment. Almost all biomarker parameters of carbonaceous mudstones are between coal and mudstones, suggesting that the organic matter sources and depositional environments for carbonaceous mudstones are between that of the coals and mudstones. The greater phytoplankton contribution to the mudstones is verified by the higher liptinite content. However, the lower organic matter abundance and the lower hydrogen index indicate that vitrinite rather than liptinite is the major hydrocarbon generation maceral. Although coal and carbonaceous mudstone have significantly higher organic matter abundance, more oil-prone kerogen types, and more gold-tube pyrolysis yields, oil-source correlation employing biomarkers and carbon isotopes suggest that mudstones are the major source rocks in the Xihu Sag. This apparent contradiction may be due to the thin layer thickness and limited distribution of the coal. The fact that more contributions of coal and carbonaceous mudstone for oils are found in the western slope belt where coal and carbonaceous mudstone were deposited seems to support this viewpoint. This contradiction may also be caused by the inability of coal to effectively expel the generated high molecular weight hydrocarbons.

Biodegradation of mixed polycyclic aromatic hydrocarbons by Pseudomonas sp. isolated from estuarine sediment

Polycyclic aromatic hydrocarbons (PAHs) are released into the environment via several natural and anthropogenic sources leading to long-term consequences that severely affect the environment, ecosystem, human and animal health. In this study, the extent of PAH pollution was measured at two estuarine locations of the major rivers of Goa, Zuari and Mandovi. Out of the 16 PAHs marked as carcinogenic, 13 PAHs were detected from the sediment samples collected. Bacterial strains were isolated from these PAH-contaminated sediments using conventional plating method. Six of these selected bacterial isolates were checked for their efficacy to degrade both low (phenanthrene) and high molecular weight (fluoranthene and pyrene) hydrocarbons. Amongst them, two bacterial isolates exhibited over 80% degradation of phenanthrene. Isolate NIOSV7 (Pseudomonas pachastrellae) could degrade 83.33% phenanthrene, 40.22% fluoranthene and 45.28% pyrene, while isolate NIOSV8, identified as Pseudomonas oleovorans, showed 85.09% phenanthrene, 70.61% fluoranthene and 67.18% of pyrene degradation in 120 h, at 100 ppm initial concentration of phenanthrene and 75 ppm of fluoranthane and pyrene. Though many Pseudomonas sp. are documented for PAH degradation, this is the first report showing PAH-degradation by Pseudomonas oleovorans strain. This study also shows that the bacteria isolated from estuarine sediments contaminated with PAH have good potential to degrade low and high molecular weight PAHs. These toxic pollutants can be bio-transformed into nontoxic metabolites with the help of microorganisms isolated from the same habitat.