Heavy Hydrocarbons Research Articles

Effects of discharge frequency on the conversion of n-hexadecane by pulsed liquid-phase discharge in recycle and batch devices

Converting hydrocarbons can make the fossil fuel industry more flexible in responding to market changes by producing various products to meet market demands. Efficient, clean, and flexible plasma processes are a highly promising technology for hydrocarbon processing and conversion. In this study, the conversion of n-hexadecane was investigated using ethanol solution-assisted pulsed liquid-phase discharge plasma. The effects of recycle and batch devices and discharge frequency on feedstocks conversions and product yields were examined. The use of a recycle device facilitated the conversion of n-hexadecane. Adjusting the frequency enabled the regulation of products concentration. High discharge frequency increased the cracking of n-hexadecane and promoted further cracking of reactants into smaller molecular products, boosting the proportion of H2 and C2 hydrocarbons, and enhancing the yield of gases and light hydrocarbons. Reducing the frequency favored polymerization reactions, resulting in the formation of heavy hydrocarbons. At a frequency of 10.2 kHz, the recycle device achieved a gas production rate of 112.1 mL/min and a gas production efficiency of 87.5 mL/kJ. With an SEI of 3202 kJ/L, the conversion of n-hexadecane was 15.5%, the yield of light hydrocarbons was 717.0 mg, and the light product selectivity was 97.1%. This study offers an efficient approach for the processing and conversion of hydrocarbons in the fossil fuel industry.

Microbially derived surfactants: an ecofriendly, innovative, and effective approach for managing environmental contaminants.

The natural environment is often contaminated with hydrophobic pollutants such as long-chain hydrocarbons, petrochemicals, oil spills, pesticides, and heavy metals. Hydrophobic pollutants with a toxic nature, slow degradation rates, and low solubility pose serious threats to the environment and human health. Decontamination based on conventional chemical surfactants has been found to be toxic, thereby limiting its application in pharmaceutical and cosmetic industries. In contrast, biosurfactants synthesized by various microbial species have been considered superior to chemical counterparts due to their non-toxic and economical nature. Some biosurfactants can withstand a wide range of fluctuations in temperature and pH. Recently, biosurfactants have emerged as innovative biomolecules not only for solubilization but also for the biodegradation of environmental pollutants such as heavy metals, pesticides, petroleum hydrocarbons, and oil spills. Biosurfactants have been well documented to function as emulsifiers, dispersion stabilizers, and wetting agents. The amphiphilic nature of biosurfactants has the potential to enhance the solubility of hydrophobic pollutants such as petroleum hydrocarbons and oil spills by reducing interfacial surface tension after distribution in two immiscible surfaces. However, the remediation of contaminants using biosurfactants is affected considerably by temperature, pH, media composition, stirring rate, and microorganisms selected for biosurfactant production. The present review has briefly discussed the current advancements in microbially synthesized biosurfactants, factors affecting production, and their application in the remediation of environmental contaminants of a hydrophobic nature. In addition, the latest aspect of the circular bioeconomy is discussed in terms of generating biosurfactants from waste and the global economic aspects of biosurfactant production.

Methods Using Marine Aquatic Photoautotrophs along the Qatari Coastline to Remediate Oil and Gas Industrial Water.

Qatar and other Gulf States have a diverse range of marine vegetation that is adapted to the stressful environmental conditions of seawater. The industrial wastewater produced by oil and gas activities adds further detrimental conditions for marine aquatic photosynthetic organisms on the Qatari coastlines. Thus, these organisms experience severe stress from both seawater and industrial wastewater. This review discusses the biodiversity in seawater around Qatar, as well as remediation methods and metabolic pathways to reduce the negative impacts of heavy metals and petroleum hydrocarbons produced during these activities. The role of microorganisms that are adjacent to or associated with these aquatic marine organisms is discussed. Exudates that are released by plant roots enhance the role of microorganisms to degrade organic pollutants and immobilize heavy metals. Seaweeds may have other roles such as biosorption and nutrient uptake of extra essential elements to avoid or reduce eutrophication in marine environments. Special attention is paid to mangrove forests and their roles in remediating shores polluted by industrial wastewater. Seagrasses (Halodule uninervis, Halophila ovalis, and Thalassia hemprichii) can be used as promising candidates for phytoremediation or bioindicators for pollution status. Some genera among seaweeds that have proven efficient in accumulating the most common heavy metals found in gas activities and biodegradation of petroleum hydrocarbons are discussed.

Calculation of the Rate Constants of Vacuum Residue Hydrogenation Reactions in the Presence of a Chrysotile/NiTi Nanocatalyst

The paper presents the results of an investigation into the kinetics of catalytic hydrogenation of vacuum residue at temperatures of 380, 400 and 420 °C and different durations, ranging from 30 to 70 min, using a nanocatalyst containing the active metals nickel and titanium supported on chrysotile. It was found that the yield of oils from 30 to 50 wt.% and tars from 12 to 18 wt.% increased with increasing temperatures and reaction times. A slight increase in the proportion of solids in the range of 2.0 to 6.0 wt.% is explained by the activity of the nanocatalyst used. In the study of the kinetics of vacuum residue hydrogenation, using the nanocatalyst developed by the authors, we were able to achieve a low yield of solids with a short contact time as well as a high yield of low-molecular-weight compounds such as oils and tars. To determine the kinetic parameters (rate constants and activation energies), Simpson’s integral method and a random search engine optimization method were used. High values of rate constants are characteristic of reactions in the formation of oils k1, tars k2 and asphaltenes k3 in the temperature range of 380–420 °C. The high values of the rate constants k1, k2 and k3 in the catalytic hydrogenation of the vacuum residue indicate the high reaction rate and activity of the nanocatalyst used. With an increase in temperature from 380 to 420 °C, the rate constant of the formation of gas products from vacuum residue and the conversion of asphaltenes into oils significantly increase, which indicates the accumulation of low-molecular-weight compounds in oils. The activation energy for reactions leading to the formation of oils, tars, asphaltenes, gas and solid products was 75.7, 124.8, 40.7, 205.4 and 57.2 kJ/mol, respectively. These data indicate that the processes of vacuum residue hydrogenation with the formation of oils and asphaltenes require the lowest energy inputs. Reducing the process temperature to increase the selectivity of the vacuum residue hydrogenation process when using the prepared nanocatalyst is recommended. The formation of oils at the initial stage plays a key role in the technology of the heavy hydrocarbon feedstock (HHF) hydrogenation process. Perhaps the resulting oils can serve as an additional solvent for high-molecular-weight products such as asphaltenes, as evidenced by the low activation energy of the process.

BIOAUGMENTATION AS BIOREMEDIATION APPROACH FOR CONTAMINATED SOIL: A REVIEW

The inevitable impacts by the emerging urbans developments towards the quality and function of soil have raised concerns for future environment consequences. Pollutants that evolved from the anthropogenic activities including heavy metals, pesticides, petroleum hydrocarbons (TPH) and polycyclic aromatic hydrocarbons (PAHs) tend to be persistent within the soil and hence, contribute to long term effects towards the environment and human’s health. Researchers discovered the success of bioaugmentation as part of bioremediation as an approach towards degrading the pollutants by employing microorganisms (i.e., bacteria or fungi) to enhance the removal of pollutants. The concept, mechanism, method, and factors affecting bioaugmentation is studied for the past years to explore the thorough process of bioaugmentation. It is claimed that bioaugmentation is directly related to the microbial activity and have three different approaches (autochthonous, allochthonous, and genetically engineering microorganisms). pH, temperature, moisture, and oxidation reduction potential are the key prospects towards bioaugmentation efficiency. The application of bioaugmentation towards each targeted pollutant are studied to certify its capability of degrading, removing, and transforming pollutants into less toxic components.

Catalytic pyrolysis of plastic waste using activated carbon from cotton waste

This study introduces a novel approach to plastic waste management and energy recovery by synthesizing highly porous activated carbon from an often-overlooked resource, waste cotton fabric (WCF), using H3PO4 as an activating agent. The synthesized waste cotton fabric activated carbon samples (WCF-AC) were utilized as a solid acid catalyst in the catalytic pyrolysis of low-density polyethylene (LDPE), with the aim of converting LDPE into fuel-range hydrocarbons. This research highlights the potential of bio-based waste materials in the synthesis of eco-friendly and cost-effective catalysts for feedstock recycling. The impact of the H3PO4 impregnation ratio and the carbonization/activation temperature on the physicochemical properties of the resulting WCF-AC samples was investigated, providing valuable insights into the optimization of activated carbon production. The catalytic activity of the synthesized WCF-AC samples was evaluated, demonstrating a reduction of 12°C in the LDPE degradation temperature. Furthermore, this work revealed a substantial increase in the formation of carbocyclic compounds, with light aromatics such as benzene, toluene, and xylene constituting up to 43 % of the pyrolysis output. In certain instances, a decrease in heavier hydrocarbons beyond C11 was observed, indicating the selective yield of specific range hydrocarbons. This study underscores the potential of bio-based acid catalysts, such as the synthesized activated carbon presented here, in plastic recycling. The approach adopted in this research aligns with the principles of the circular economy, promoting resource efficiency and sustainability.

Evaluation of heavy hydrocarbon liquid in the Eastern Dahomey Basin, Southwestern Nigeria (case study of Agbabu Bitumen in Ondo State)

Solvent-aided dilution processes are often employed to recover bitumen by reducing its viscosity. In this study, methanol, toluene, and xylene were investigated as potential hydrocarbon solvents for solvent-aided hydrocarbon recovery of Agbabu bitumen. To achieve this, the solubility of the sample in the solvents was determined with a solubility test, its viscosity was measured with the Saybolt Furol Viscometer using the ASTM D88 method, and its SARA analysis was conducted using high-performance liquid chromatography. Agbabu bitumen was found to have a high content of saturates and aromatics. Viscosity decreases as pressure increases, while solubility reduces as temperature increases. The sample was most soluble in toluene, and its viscosity was reduced most in it, followed by xylene. Methanol reduced the saturates content and significantly raised the asphaltene content, keeping the mixture viscosity high. In terms of asphaltene stability of the mixtures, the bitumen-methanol system with the lowest colloidal instability index of 0.874 will give a mild asphaltene deposit issues compared with others that are unstable. This approach of combining multiple tests with the CII can accurately predict the behavior of Agbabu bitumen in solvents and enhance decision on the choice of bitumen recovery technology.

“Component flow” conditions and its effects on enhancing production of continental medium-to-high maturity shale oil

Based on the production curves, changes in hydrocarbon composition and quantities over time, and production systems from key trial production wells in lacustrine shale oil areas in China, fine fraction cutting experiments and molecular dynamics numerical simulations were conducted to investigate the effects of changes in shale oil composition on macroscopic fluidity. The concept of “component flow” for shale oil was proposed, and the formation mechanism and conditions of component flow were discussed. The research reveals findings in four aspects. First, a miscible state of light, medium and heavy hydrocarbons form within micropores/nanopores of underground shale according to similarity and intermiscibility principles, which make components with poor fluidity suspended as molecular aggregates in light and medium hydrocarbon solvents, such as heavy hydrocarbons, thereby decreasing shale oil viscosity and enhancing fluidity and outflows. Second, small-molecule aromatic hydrocarbons act as carriers for component flow, and the higher the content of gaseous and light hydrocarbons, the more conducive it is to inhibit the formation of larger aggregates of heavy components such as resin and asphalt, thus increasing their plastic deformation ability and bringing about better component flow efficiency. Third, higher formation temperatures reduce the viscosity of heavy hydrocarbon components, such as wax, thereby improving their fluidity. Fourth, preservation conditions, formation energy, and production system play important roles in controlling the content of light hydrocarbon components, outflow rate, and forming stable “component flow”, which are crucial factors for the optimal compatibility and maximum flow rate of multi-component hydrocarbons in shale oil. The component flow of underground shale oil is significant for improving single-well production and the cumulative ultimate recovery of shale oil.

Shale oil recovery by CO2 injection in Jiyang Depression, Bohai Bay Basin, East China

Laboratory experiments, numerical simulations and fracturing technology were combined to address the problems in shale oil recovery by CO2 injection. The laboratory experiments were conducted to investigate the displacement mechanisms of shale oil extraction by CO2 injection, and the influences of CO2 pre-pad on shale mechanical properties. Numerical simulations were performed about influences of CO2 pre-pad fracturing and puff-n-huff for energy replenishment on the recovery efficiency. The findings obtained were applied to the field tests of CO2 pre-pad fracturing and single well puff-n-huff. The results show that the efficiency of CO2 puff-n-huff is affected by micro- and nano-scale effect, kerogen, adsorbed oil and so on, and a longer soaking time in a reasonable range leads to a higher exploitation degree of shale oil. In the “injection + soaking” stage, the exploitation degree of heavy hydrocarbons is enhanced by CO2 through its effects of solubility-diffusion and mass-transfer. In the “huff” stage, crude oil in large pores is displaced by CO2 to surrounding larger pores or bedding fractures and finally flows to the production well. The injection of CO2 pre-pad is conducive to keeping the rock brittle and reducing the fracture breakdown pressure, and the CO2 is liable to filter along the bedding surface, thereby creating a more complex fracture. Increasing the volume of CO2 pre-pad can improve the energizing effect, and enhance the replenishment of formation energy. Moreover, the oil recovery is more enhanced by CO2 huff-n-puff with the lower shale matrix permeability, the lower formation pressure, and the larger heavy hydrocarbon content. The field tests demonstrate a good performance with the pressure maintained well after CO2 pre-pad fracturing, the formation energy replenished effectively after CO2 huff-n-puff in a single well, and the well productivity improved.

The Effect of Individual Hydrocarbons in the Composition of Diesel Fuel on the Effectiveness of Depressant Additives

The use of depressant additives is the most effective and cost-effective way to improve the low-temperature properties of diesel fuels, like the cloud point, cold filter plugging point and pour point. However, the effectiveness of depressant additives depends on the composition of the diesel fuel and the content of certain groups of hydrocarbons in it. In this work, the effect of adding individual hydrocarbons of various groups and structures on the effectiveness of depressant additives is studied. This study is carried out on model aromatic (toluene, tetralin) and n-paraffin hydrocarbons (cetane, heptadecane, heneicosane, docosane) in various concentrations. It is shown that the most negative effect on the depressant additives’ effectiveness is due to the content of the most polar aromatic hydrocarbons and light n-paraffins in the composition of diesel fuel, and the most positive effect is exerted by the content of heavy n-paraffins in small quantities. It is proposed to involve small concentrations (1–3% vol.) of heavy n-paraffin hydrocarbons (heneicosane, docosane) to increase the effectiveness of the depressant additive. It has been established that for the more effective action of the depressant, it is necessary to take into account the content and structure of individual hydrocarbons in the diesel fuel’s composition.

STUDY OF THE EFFECT OF SUPERCRITICAL WATER ON SOLID PRODUCTS OBTAINED AFTER CRACKING

One of the possible applications of supercritical water is the conversion of heavy hydrocarbon feedstocks with a high content of resins and asphaltenes. The use of supercritical water makes it possible to reduce the yield of solid products and increase the yield of light fractions. In this work, a comparative analysis of the cracking processes of petroleum residue, asphaltenes and resins isolated from it was carried out in an environment of supercritical water and without water. The experiments were carried out in an autoclave at a temperature of 450 °С and a pressure of up to 47 MPa. Cracking duration – 60 min. Cracking of petroleum residue, as well as its individual components - resins and asphaltenes, in a supercritical water environment - showed a positive effect on conversion; in all experiments, the yield of solid products decreased and the yield of maltenes increased. Solid products were studied using X-ray diffraction and thermogravimetric analysis and scanning electron microscopy. Using X-ray diffraction analysis, the influence of supercritical water on the parameters of the macrostructure was studied. It was determined that cracking with water affects the increase in the distance between saturated fragments of molecules (dr) in the structure of solid cracking products in comparison with products obtained without water. Using scanning electron microscopy, the surface of particles of insoluble cracking products was characterized. Solid products obtained in a supercritical water environment have a porous surface. According to thermal analysis data, it is shown that solid products obtained by cracking in water are characterized by more intense dynamics of sample weight loss and a smaller residue at the final temperature. For citation: Nalgieva Kh.V., Kopytov M.A. Study of the effect of supercritical water on solid products obtained after cracking. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 8. P. 113-120. DOI: 10.6060/ivkkt.20246708.14t.

The Influence of Pt Additives on The Activity and Stability of Rh-containing Catalyst Performance in Diesel Fuel Conversion into Syngas

The influence of platinum additives on the properties of rhodium catalysts in steam and autothermal reforming processes of diesel fuel was investigated. It was found that the Rh/CZF catalyst exhibited higher activity, with a higher degree of fuel conversion and lower production of side reaction products compared to the bimetallic Rh–Pt/CZF catalyst. The proposed two-zone catalytic Pt/CZF+Rh/CZF structured honeycomb catalyst demonstrated stable performance and high activity in autothermal reforming of commercial diesel fuel. However, the presence of platinum in the frontal zone of the catalyst reduced its resistance to coking compared to the rhodium-containing sample. The obtained results are of practical significance in the development of efficient systems for the conversion of heavy hydrocarbons into synthesis gas.

Drifting long-lived. To the 50ʰᵗ anniversary of the opening of the “North Pole-22” station

The national drifting station “North Pole-22” (NP-22 or SP-22) had been opened on September 13, 1973 in the Arctic on the big ice island and operated for 3130 days. Now it is the longest operating observational station in the history of Arctic studies of the USSR and the Russian Federation. For eight and a half years, its total drift amounted 17,069 km. During that period a wide complex of scientific programs in oceanography, geophysics, meteorology, glaciology, hydrography, hydrobiology was carried out here. In addition, field tests and implementation of new types of scientific instruments and introduction of new expeditionary polar equipment into the observation practice were performed. For the first time in the practice of the drifting NP/SP stations, oblique sounding of the ionosphere, observations of fine thermohaline structure of waters of the active layer of the Arctic Ocean were carried out. Geographical coordinates of the station drift were determined using Soviet satellite navigation systems; a complex for recording satellite images of the ice cover was deployed; investigations of the arctic ecosystems were made. Specific experiments were conducted aimed at the natural decomposition of heavy hydrocarbons by the ultraviolet solar radiation. The ice airfield of this station received 1,511 flights of aircraft and helicopters, delivering 2,961 tons of expedition cargos. Landings on this airfield were provided by flight teams of the High-Latitude Air Expedition “Sever” of the Arctic and Antarctic Research Institute and the Hydrographic Service of the Northern Fleet. Foreign specialists repeatedly visited the station. For the nine rotations of polar explorers who worked at the NP/SP-22, its personnel amounted to 249 people, many of them several times worked at this drifting station in different years. The work of the NP/SP-22 team was appreciated by the government authorities of the USSR.

Ecological and human health risk associated with heavy metals (HMs) contaminant sourced from petroleum refinery oily sludge

The environmental and human health risk of heavy metals (HMs) in petroleum based oily sludge (OS) varies depending upon the source of origin of the crude oil and treatment processes practiced at the refineries. Consequently, the present study explores the potential risk associated with HMs of OS obtained from different refinery sites to the environment and human health. The results showed that HMs (Cu, Ni, Zn, Mn) present in OS surpasses the permissible limit of WHO guidelines except for Cr. Additionally, the Igeo value (grade 3–6), Ef (2.48–121.4), PLI (5.12–22.65), Cd (32.48–204.76) and PERI (grade 1–5) confirmed the high level of HMs contamination into the OS and its risk to the environment. Besides, the hazard index (HI) and the total carcinogenic risk (TCR) for HMs show substantial risk to both adult and children health. Likewise, the G-mean enzyme index and potential soil enzyme risk index (PSERI) of the OS showed a high risk to soil biological properties. Furthermore, statistical analysis confirmed the heterogeneity in properties of the OS and its potential impact on the soil ecosystem arising from different sites. Finally, the study unveils a novel perspective on the environmental and human health consequences associated with the OS.

REMEDIATION OF SOILS CONTAMINATED WITH HEAVY FRACTION HYDROCARBONS USING BIOSURFACTANTPRODUCED BYPSEUDOMONAS SP.

This study evaluated the effectiveness of the biosurfactant generated by a strain of Pseudomonas sp. in the removal of heavy fraction hydrocarbons from a soil contaminated with 28,000 mg/kg, by a washing process. The efficacy of the biosurfactant was compared to that of a chemical surfactant, used at a concentration of 0.1%. After five wash cycles, the biosurfactant reached a maximum removal efficiency of 42.71%, in contrast to that of the chemical surfactant, 32.31%. In addition, bioaugmentation with the culture medium used for the production of the biosurfactant was evaluated, with a removal of 38.29% of these hydrocarbons in 90 days.

Experimental and numerical investigations of soot formation in propane laminar coflow flames in O2/N2 and O2/CO2 atmospheres

Oxygen-rich combustion is a new type of clean combustion technology with important application prospects. At present, there are few detailed analyses on the mechanism changes of soot formation under oxygen enrichment of propane. In this paper, the effects of oxygen-rich (O2/N2, O2/CO2) combustion on soot formation in the propane laminar flow coaxial jet diffusion flame were investigated by using the experiment and numerical simulation. The flame image was taken by a color (CCD) camera in the visible band, and the two-dimensional distribution of temperature and soot volume fraction in the flame was reconstructed. In numerical simulation, the soot production model considers a detailed description of nucleation via collisions among heavy polycyclic aromatic hydrocarbons, particle aggregation, polycyclic aromatic hydrocarbons condensation, surface growth and oxidation through the hydrogen abstraction acetylene addition mechanism. The results show that the experimental results were compared with the numerical simulation results, and the numerical simulation results predict the temperature and soot change of oxygen-rich flame well. With the increase in oxygen concentration, the peaks of soot and temperature in the two oxygen-rich atmospheres gradually increased. With the increase in oxygen concentration, the peaks of soot and temperature in the two oxygen-rich atmospheres gradually increased. Comparing the combustion mechanism changes of the two oxygen-rich combustion systems, it was found that the hydrogen abstraction acetylene addition mechanism was the main cause of soot generation. The OH oxidation is dominated near the fuel nozzle side, and O2 oxidation is dominant downstream. With the substitution of CO2 for N2, the chemical effect of CO2 reduces the flame temperature and inhibits the formation mechanism and oxidation mechanism of soot to some extent. This in turn leaded to a reduction in the amount of soot produced.

Sonochemical and mechanochemical synthesis of iron-based nano-hydrotalcites promoted with Cu and K as catalysts for CO and CO2 Fischer-Tropsch synthesis

A novel class of Fe-based nano hydrotalcites as catalysts for Fischer-Tropsch (FT) synthesis, with a focus on CO2 hydrogenation have been prepared, characterized and tested. These catalysts were synthesized using two green, energy- and time-saving synthesis methods: ultrasound-assisted co-precipitation and solvent-free mechanochemical syntesis. The catalysts demonstrate very satisfactory CO and CO2 conversion capacities, in particular with good selectivities towards heavy hydrocarbons. The ultrasound-processed variant is particularly noteworthy, displaying about 10 % higher activity under specific conditions. The unique physicochemical properties of these catalysts, which were extensively characterized by XRD, TGA, (ATR) FT-IR, ICP-OES, SEM, TEM, BET, and TPR, are responsible for their remarkable potential for CO and CO2 conversion with varied product distribution. These findings highlight as these iron-based hydrotalcites can be considered as a new promising class of catalyst for CO and CO2 conversion by Fischer-Tropsch reaction.

Development of predictive model for determination of paraffin deposition in Kazakh crude oil

Kazakhstan's crude oil contains significant amounts of heavy hydrocarbons that solidify as wax at lower temperatures, leading to reduced flow rates and potential blockages in pipelines. Paraffin, a substantial component of crude oil, crystallizes below its pour point, posing challenges for maintaining efficient crude oil transportation. Addressing wax deposition is essential for optimizing oil flow and meeting global energy demand. This article presents an innovative method for forecasting paraffin deposition in Kazakh crude oil, using its chemical composition and thermobaric conditions. The methodology encompassed data analysis, ASTM-standard laboratory tests, and computations employing modified equations for fusion properties calculation. Outcomes comprise computed temperatures, enthalpy, and heat capacity related to melting, along with revised correlations for melting and pour points specific to Kazakh crude oils. The melting point correlation was modified to fit the properties of Kazakh crude oils, resulting in standard deviation of 0.55 %. Computed pour points for hydrocarbons improved by 17 % respectively. As a result of the research a novel software tool was developed and evaluated, highlighting the project’s contribution in providing an adjusted thermodynamic model for paraffin deposition forecasting. Comparisons between the developed software, PVTSim, and field data showed the wax appearance temperature (WAT) predictions closely aligned, with 0.74 % of error. This numerical tool shows potential in predicting wax deposition, thus aiding in the planning of oil production and refining processes in Kazakhstan. The importance of this work extends to its potential economic impact on companies and the nation, as well as its environmental benefits by facilitating eco-friendly planning of oil production facilities. Future research could expand on these findings to further enhance predictive models of paraffin precipitation across diverse conditions

OIL FAMILIES AND GEOCHEMICAL COMPOSITION OF DEVONIAN OILS AT THE RECHITSA FIELD, PRIPYAT BASIN, BELARUS

The sedimentary column at the Rechitsa oilfield in the Pripyat rift basin, Belarus, is dominated by an Upper Devonian synrift succession. The succession includes uppermost Frasnian and mid‐Famennian salt units which are about 1000 m and 2000 m thick respectively. Reservoir rocks consist of sandstones and carbonates in the intra‐, inter‐ and sub‐salt successions. In this paper, the geochemical analysis of 15 oil samples from different stratigraphic intervals at the Rechitsa field is used as a basis for reservoir characterisation. Geochemical studies included biomarker and stable C, N and S isotope analyses.Four genetic oil groups were identified and are referred to as Groups A to D. Oils in Group A came from upper intra‐ and inter‐salt reservoir rocks; the oils are early mature, enriched in heavy (C36+) hydrocarbons, heteroatoms, aryl‐isoprenoids and gammacerane, with low Pr/Ph = 0.6 and a sulphur isotope composition averaging 22.7‰ CDT. Oils in Group B were from sub‐salt reservoirs and are at peak maturity with Pr/Ph = 1, an increased proportion of C27 regular steranes, and a sulphur isotope composition of 8.1‰ CDT. The single oil sample in Group C was from a Proterozoic reservoir. The oil was overmature with a low content of heavy fractions, heteroatoms and steranes; its hopanes composition indicated that it was generated by the same source rock as the oils in Group B. Oils in Group D came from inter‐salt reservoir rocks and were composed of a mixture of Groups A and B oils in roughly equal proportions, as indicated by their average isotope, molecular and biomarker compositions.Observed differences in oil composition were explained in terms of contributions from at least two different source rocks together with variations in source rock maturity. Group A oils were interpreted to have been generated by Famennian carbonate‐rich source rocks containing dominantly marine and bacterial organic matter deposited in an anoxic evaporitic setting. Source rocks for Groups B and C oils were suggested to be composed of OM‐rich marine shales of Frasnian age or older.The geochemical characteristics of the Devonian oils from Rechitsa field, and the oil‐oil and oil‐ source rock correlations reported, will contribute to a better understanding of the petroleum system in the Pripyat Basin although direct oil‐ source rock correlations are not yet available. The presence of at least two source rocks for the Rechitsa oils has been suggested, respectively comprising carbonates in the inter‐salt succession and marine shales and/or carbonates in the sub‐salt succession. The main controls on oil composition in the Devonian reservoir units were the varying contributions from the different source rocks and differences in source rock thermal maturity associated with variations in burial depth and tectonics, together with the stratigraphic distribution of reservoir units which was in turn controlled by the presence of the thick Frasnian and Famennian salt units.

Possibilities of spectral analysis methods for the oil sludge research

The paper considers the problem of utilisation and neutralisation of oil sludge at oil producing and refining enterprises. Oil sludge is a complex heterogeneous mixture consisting of high-molecular oil compounds, mineral particles of different composition, and water. The authors studied the elemental composition of oil sludge of different storage periods for oil refinery production by modern analytical methods: IR spectroscopy and X-ray fluorescence spectrometry. According to the research, the main composition of the oil residue, represented by the hydrocarbon component, contains paraffin-naphthenic and heavy aromatic hydrocarbons. Moreover, its non-hydrocarbon component contains compounds Si, Al, Ca, Fe, S, Ba.