Quantitatively unmixing method for complex mixed oil based on its fractions carbon isotopes: A case from the Tarim Basin, NW China

Deep mixed oils with secondary alterations have been widely discovered in the Tarim Basin,but current methods based on biomarkers and isotopes to de-convolute mixed oil cannot calculate the exact mixing proportion of different end-member oils,which has seriously hindered further exploration of deep hydrocarbons in the study area.To solve this problem,we constructed a novel method based on the carbon isotope(δ13C)of the group components to de-convolute mixed liquid hydrocarbons under the material balance principle.The results showed that the mixed oil in the Tazhong Uplift was dominantly contributed at an average proportion of 68% by an oil end-member with heavier d13C that was believed to be generated from the Cambrian-Lower Ordovician source rocks,whereas the mixed oil in the Tabei Uplift was predominantly contributed at an average proportion of 61% by an oil end-member with lighter d13C that was believed to be generated from the Middle-Upper Ordovician source rocks.This indicates that,on the basis of the detailed description of the distribution of effective source rocks,the proposed method will be helpful in realizing differential exploration and further improving the efficiency of deep liquid hydrocarbon exploration in the Tarim Basin.In addition,compared to traditional δ13C methods for whole oil and individual n-alkanes in de-convoluted mixed oil,the proposed method has a wider range of applications,including for mixed oils with variations in color and density,indicating potential for promoting the exploration of deep complex mixed oils in the Tarim Basin and even around the world.

Accumulation and Mixing of Oils in Jinghu Sag of Subei Basin:Constraints from Thermal Maturity Parameters

Oils in Jinghu sag are abundant with high content of polar compounds and have a low ratio of saturate to aromatic hydrocarbons and a high ratio of resin to asphaltene. The gross composition of oils in the Jinghu sag suggests typical immature to low mature characteristics. Some compounds with low thermal stability were identified. Light hydrocarbons, a carbon preference index, an odd even index, n-alkane and hopane maturity parameters show mature features and little differences in the maturity level among oils. Sterane isomerization parameters indicate an immature to low mature status of oil. Transfer of the sedimentary center during sedimentation has led to different thermal histories among subsags and thus generated oils with different maturities. On the basis of source analyses, four migration and accumulation patterns with different maturity can be classified. Combined with available information on mergers of source, reservoir and long distance oil lateral migration, mixing conditions were present in the Jinghu sag. Experimental results indicate that maturity variations are caused by mixtures of hydrocarbons with different maturity.

Application of Biomarkers to Quantitative Source Assessment of Oil Pools

Recent detailed organic geochemical and geological investigation indicate that oils of the Bamianhe oilfield, Bohai Bay Basin, East China are the mixture of less mature oils and normal oils derived from the ES4 mudstones and shales with a wide range of thermal maturity from immature to middle-maturity, and most of the oils were proved to be sourced from the depocenter of the Niuzhuang Sag immediately adjacent to the Bamianhe oilfield. Two approaches to quantify the amount of immature oils mixed through quantitative biomarkers were established. One is a relatively simple way only through organic geochemical analysis while the other is to be combined with basin modeling. Selecting biomarkers as proxies is the crucial point in both of them. The results show that the less mature oils mixed in the Bamianhe oilfield is less than 10% and 18% respectively based on the two approaches, which coincide with the results of oil-source rock correlation.

Oil-source rock correlation and quantitative assessment of Ordovician mixed oils in the Tazhong Uplift, Tarim Basin

The origin of the marine oils in the Tarim Basin has long been a disputed topic. A total of 58 DST （drill stem test） crude oil and 8 rock samples were investigated using a comprehensive geochemical method to characterize and identify the origin of the Ordovician oils in the Tazhong Uplift, Tarim Basin, northwest China. Detailed oil–oil and oil–source rock correlations show that the majority of the oils have typical biomarker characteristics of the Middle-Upper Ordovician （O2＋3） source rock and the related crude oil. These characteristics include a distinct ＂V-shaped＂ relative abundance of C27, C28 and C29 regular steranes, low abundance of dinosterane, 24-norcholestanes, triaromatic dinosteroids and gammacerane. Only a few oils display typical biomarker characteristics indicating the Cambrian–Lower Ordovician （∈-O1） genetic affinity, such as linear or anti ＂L＂ shape distribution of C27, C28 and C29 regular sterane, with relatively high concentrations of dinosterane, 24-norcholestanes, triaromatic dinosteroids and gammacerane. It appears that most of the Ordovician oils in the Tazhong Uplift were derived from the O2＋3 intervals, as suggested by previous studies. However, the compound specific n-alkane stable carbon isotope data indicate that the Ordovician oils are mixtures from both the ∈-O1 and O2＋3 source rocks rather than from the O2＋3 strata alone. It was calculated that the proportion of the∈-O1 genetic affinity oils mixed is about 10.8%-74.1%, with an increasing trend with increasing burial depth. This new oil-mixing model is critical for understanding hydrocarbon generation and accumulation mechanisms in the region, and may have important implications for further hydrocarbon exploration in the Tarim Basin.

A Mathematical Calculation Model Using Biomarkers to Quantitatively Determine the Relative Source Proportion of Mixed Oils

It is difficult to identify the source（s） of mixed oils from multiple source rocks, and in particular the relative contribution of each source rock. Artificial mixing experiments using typical crude oils and ratios of different biomarkers show that the relative contribution changes are non-linear when two oils with different concentrations of biomarkers mix with each other. This may result in an incorrect conclusion if ratios of biomarkers and a simple binary linear equation are used to calculate the contribution proportion of each end-member to the mixed oil. The changes of biomarker ratios with the mixing proportion of end-member oils in the trinal mixing model are more complex than in the binary mixing model. When four or more oils mix, the contribution proportion of each end-member oil to the mixed oil cannot be calculated using biomarker ratios and a simple formula. Artificial mixing experiments on typical oils reveal that the absolute concentrations of biomarkers in the mixed oil cause a linear change with mixing proportion of each end-member. Mathematical inferences verify such linear changes. Some of the mathematical calculation methods using the absolute concentrations or ratios of biomarkers to quantitatively determine the proportion of each end-member in the mixed oils are deduced from the results of artificial experiments and by theoretical inference. Ratio of two biomarker compounds changes as a hyperbola with the mixing proportion in the binary mixing model, as a hyperboloid in the trinal mixing model, and as a hypersurface when mixing more than three end- members. The mixing proportion of each end-member can be quantitatively determined with these mathematical models, using the absolute concentrations and the ratios of biomarkers. The mathematical calculation model is more economical, convenient, accurate and reliable than conventional artificial mixing methods.

Characteristics of the sea ice reflectance spectrum polluted by oil spills based on field experiments in the Bohai Sea

Oil spilled on the sea ice surface in the Bohai Sea of China is studied through the field measurements of the reflectance of a simulated sea ice-oil film mixed pixel. The reflection characteristics of sea ice and oil film are also analyzed. It is found that the mixed pixel of sea ice and oil film is a linear mixed pixel. The means of extracting sea ice pixels containing oil film is presented using a double-band ratio oil-film sea-ice index（DROSI） and a normalized difference oil-film sea-ice index（NDOSI） through the analysis of the reflectance curves of the sea iceoil film pixel for different ratios of oil film. The area proportion of the oil film in the sea ice-oil film pixel can be accurately estimated by the average reflectance of the band of 1 610–1 630 nm, and the volume of the spilled oil can be further estimated. The method of the sea ice-oil film pixel extraction and the models to estimate the proportion of oil film area in the sea ice-oil film pixel can be applied to the oil spill monitoring of the ice-covered area in the Bohai Sea using multispectral or hyperspectral remote sensing images in the shortwave infrared band（1 500–1 780 nm）.

Modeling and optimization for oil well production scheduling

In this paper,an oil well production scheduling problem for the light load oil well during petroleum field exploitation was studied.The oil well production scheduling was to determine the turn on/off status and oil flow rates of the wells in a given oil reservoir,subject to a number of constraints such as minimum up/down time limits and well grouping.The problem was formulated as a mixed integer nonlinear programming model that minimized the total production operating cost and start-up cost.Due to the NP-hardness of the problem,an improved particle swarm optimization(PSO) algorithm with a new velocity updating formula was developed to solve the problem approximately.Computational experiments on randomly generated instances were carried out to evaluate the performance of the model and the algorithm's effectiveness.Compared with the commercial solver CPLEX,the improved PSO can obtain high-quality schedules within a much shorter running time for all the instances.

Source and accumulation process of Jurassic biodegraded oil in the Eastern Junggar Basin,NW China

Biodegradation usually obscures or even radically alters the original characteristics of oil biomarkers.The mixing of oil from multiple sources makes each source difficult to trace.Identifying the source of biodegraded oil from multiple sources has always been a hard nut to crack.Rising to this challenge,in this study-we carried out a comprehensive investigation of biodegradation impacts,oil-source correlation,and oil charging history to trace the source and reveal the mixing process of biodegraded oil in the Toutunhe Formation(J_(2)t)in the eastern Junggar Basin,NW China.The oil of this area was biodegraded to different extent,consequently,many commonly used biomarker parameters(e.g.Pr/Ph,Pr/n C_(17))became less powerful for oil-source correlation.To address this problem,the resistance of many biomarkers to biodegradation was analyzed,and those of high bio resistance were selected to generate a more reliable oil-source correlation.The results revealed that biodegraded oil was a mixture of oil sourced from Lucaogou Formation(P_(2)l)and Xiaoquangou Formation(T_(2-3)xq).Core sample observation,microscopic fluorescent analysis and fluid inclusion analysis were combined to analyze comprehensively oil charging history.The analysis of accumulation process exhibited that the existing oil in J_(2)t was a mixture originated from the P_(2)l and T_(2-3)xq source rocks in two separate charging stages when it underwent a complicated process of charging,biodegradation,recharging and mixing.

Geochemical significances of 8,14-secohopanes in marine crude oils from the Tazhong area in the Tarim Basin,NW China

8,14-secohopanes in the marine oils from the Tazhong area in the Tarim Basin are detected by gas chromatography-mass spectrometry(GC-MS)and gas chromatography-mass spectrometry-mass spectrometry(GC-MS-MS),and their distributions and compositions are compared in order to study their potential significances in oil-source correlation.C35+extended hopane series and three series of extended 8,14-secohopanes can be detected in two kinds of end-member oils in the Tazhong area in the Tarim Basin,and they are different in distribution,suggesting that they may have some special geochemical significance.The presence of 8,14-secohopanes in two kinds of end-member oils in the Tarim Basin suggests that these biomarkers are primary,and not related to biodegradation.The relative abundance of 8,14-secohopanes in the type-A oil is much less than that in the type-B oil,and the 8,14-secohopanes content in end-member oils is much less than that in the corresponding mixed oils.Based on the relative contents of 8,14-secohopanes and the compositions of common steranes and triterpanes,it is very effective to distinguish different crude oils from the Tazhong area.The great difference in the relative abundance of 8,14-secohopanes between the type-A oil and type-B oil suggests that their formation may require some specific geological-geochemical conditions.

Comparative Evaluation of the Thermal Aging of Solid Insulation in Mineral Oil and Methyl Ester of Palm Kernel Oil

The purpose of this work is to determine the impact of thermal aging on the dielectric and physicochemical properties of the oil/paper mixed insulation. We performed a comparative analysis of dielectric paper dipped in two cooling fluids: palm kernel oil methyl ester (MEPKO) and mineral oil (MO). Two types of dielectric paper were used: Thermally Upgraded Kraft paper (TUK) and Nomex-910 paper (NP-910). An accelerated aging test was realized at 110°C during a total of 96 hours. Samples of oil and paper were collected after 0, 48, 72 and 96 hours for analyses purposes. The analyses performed included the measurement of the Breakdown voltage (BDV) of the dielectric papers, the Total Acid Number (TAN) and the Decay Dissolved Products (DDP) of the liquid dielectrics. The BDV of NP-910 is greater than the BDV of TUK. Concerning the type of oil, the BDV of dielectric papers impregnated with MEPKO is greater than the BDV of similar papers impregnated with MO, indicating a better preservation of paper when dipped in methyl esters. The analyses of TAN and DDP revealed that Nomex-910 improves the oxidation stability of MO, but reduces the oxidation stability of MEPKO. These results prove that methyl esters can be used as a substitute to replace mineral oils in power transformers. Furthermore, they show that NP can be used mainly in areas of transformer where solid insulation is subjected to high thermal and electrical stress, and TUK other places where solid insulation is required. Such combination could assure money savings and a better preservation of the oil viscosity.

Changes in China--Beijing is seeking less energy-intensive economic growth ＆ a less carbon-intensive energy mix and its impact over oil ＆ gas supply

Having experienced over 30 years of rapid growth,China’s economic development is entering a new normal featured by an ever optimizing economic structure shifting from high-speed to medium-high speed growth,and from factor-driven to innovation-driven pattern.In adapting

Development of Mixed Insulation Oil as Alternative Liquid Dielectric:A Review

Use of traditional mineral oil(MO)as a liquid insulation in transformers has spanned more than 130 years.However,MO has poor heat resistance,a low ignition point,and is a non-renewable resource,which does not meet development requirements for high-performance and environmentally friendly insulation oil.Consequently,researchers have explored alternatives such as natural ester(NE)and synthetic ester(SE)oils,as well as mixed insulation oils.Mixed insulating oil is a blend of diverse insulating oil types,with optimal performance achieved by adjusting proportions of base oils.This article summarizes the innovative achievements and development of mixed insulation oil in terms of development of mixed ratio,basic physical chemical properties,electrical properties,thermal stability,and application including operation and maintenance technology.Through these efforts,this article aims to provide recommendations for future development of mixed insulating oils to advance liquid dielectric research based on enhancement mechanisms.

Mixing Characteristics of Oil Inclusions with Different Thermal Maturities in the Wenliu Uplift,Dongpu Depression,Bohai Bay Basin,North China

Multiple types of oil inclusions with different fluorescence colors have been detected in the northern Dongpu depression.Recent evidences show that these inclusions may have been trapped simultaneously or during a very short period.Therefore,whether these oils were mixed before trapping is unknown.In this study,we analyzed the petrography and fluorescence spectral characteristics of oil inclusions in the Wenliu uplift in the northern Dongpu depression,and assessed the data with the oil mixing ratio curve obtained in the previous experiment.The results show that there are three types of oil inclusions(type I,type II and type III)with yellow,green and blue fluorescence colors,corresponding to low-mature,medium-mature and high-mature oil,respectively.The"pure"oil inclusions,do exist in type II and type III group of oil inclusions,showing the medium-mature oil was generated from the source rock rather than being formed by the mixture of high-mature and low-mature end oils.Most of the oil inclusions are mixtures of high-mature and medium-mature end oils from the sub-sags to the Wenliu uplift,the mixing degree increases to close to 50%.The oil between the Qianliyuan sub-sag and the Wenliu uplift was mainly mixed by medium mature oils,whereas the oil between the Liutun sub-sag and the Wenliu uplift was mainly mixed by high mature oil.

Emissions of particulate matter and associated polycyclic aromatic hydrocarbons from agricultural diesel engine fueled with degummed,deacidified mixed crude palm oil blends

Mixed crude palm oil （MCPO）, the mixture of palm fiber oil and palm kernel oil, has become of great interest as a renewable energy source. It can be easily extracted from whole dried palm fruits. In the present work, the degummed, deacidified MCPO was blended in petroleum diesel at portions of 30% and 40% by volume and then tested in agricultural diesel engines for long term usage. The particulates from the exhaust of the engines were collected every 500 hr using a four-stage cascade air sampler. The 50% cut-off aerodynamic diameters for the first three stages were 10, 2.5 and 1μm, while the last stage collected all particles smaller than 1 μm. Sixteen particle bounded polycyclic aromatic hydrocarbons （PAHs） were analyzed using a high performance liquid chromatography. The results indicated that the size distribution of particulate matter was in the accmnulation mode and the pattern of total PAHs associated with fine-particles （〈 1 μm） showed a dominance of larger molecular weight PAHs （4--6 aromatic rings）, especially pyrene. The mass median diameter, PM and total PAH concentrations decreased when increasing the palm oil content, but increased when the running hours of the engine were increased. In addition, Commercial petroleum diesel （PB0） gave the highest value of carcinogenic potency equivalent （BaPeq） for all particle size ranges. As the palm oil was increased, the; BaPeq decreased gradually. Therefore the degununed-deacidified MCPO blends are recommended for diesel substitute.