Spectrophotometric Measurement of Asphaltene Concentration

Typically, when ultraviolet and visible absorbance of asphaltenes is employed to measure asphaltene concentration, linear calibrations of absorbance vs. asphaltene concentration are prepared from a sample of asphaltenes in a given solvent. This calibration is shown to be sensitive to: (a) the inorganic solids content of the asphaltenes; (b) physical-chemical differences between asphaltenes from different sources or extracted with different methods; and (c) selective adsorption of asphaltenes on liquid-liquid or solid-liquid interfaces. Calibration constants were determined at wavelengths of 288 and 800 nm for samples of Athabasca and Cold Lake asphaltenes obtained using different extraction methods, from precipitation experiments, and from adsorption experiments on water-in-hydrocarbon emulsions and on powdered metals. It was found that the inorganic solids content did not affect absorbance but the asphaltene concentrations must be corrected to a solids-free basis for accurate results. Calibration constants were found to correlate to the average associated molar masses of the asphaltenes. Therefore, any change in molar mass of asphaltenes during the course of an experiment may change the calibration constant. Partial precipitation and the selective adsorption of asphaltenes can lead to a change in the molar mass of asphaltenes left in solution. The corresponding change in the calibration constants can lead to errors of 5-25% in the estimated concentration.     

Variation in Composition of Subfractions of Petroleum Asphaltenes

Boscan asphaltenes were precipitated from the crude oil using mixtures of toluene and heptane at temperatures of 24, 50, and 80°C. Another process of extracting solid n-heptane asphaltenes (24°C) using the same solvent systems and temperatures was also investigated. Asphaltene yield is different by the two processes at similar conditions although both increases in temperature or toluene content lead to lower solid yield. This way the asphaltene continuum was investigated from incipient flocculation to total n-heptane precipitated asphaltenes. The asphaltenes were analyzed using elemental analysis, fluorescence spectroscopy, vapor pressure osmometry, and HPLC size exclusion chromatography. The distribution of porphyrins was also measured using absor-bance spectroscopy. The asphaltenes were found to follow a regular trend in elemental ratios, H/C and N/C, indicating increased aromaticity and nitrogen content as the solid yield decreases. Also the molecular weight was seen to increase. Size exclusion chro-matograms and fluorescence spectra were found to be different comparing solids from the two separation processes. This indicates that the asphaltene fractions obtained by extraction of solid asphaltenes are altered relative to asphaltenes obtained by ordinary precipitation. The porphyrin concentration was found to diminish rapidly with solid yield decrease in both precipitation and extraction experiments, the latter fractions, however, containing significantly less asphaltenes indicating an adsorption step in the coprecipitation of porphyrins. Soluble fractions were found to exhibit relatively low molecular weights and an apparent lack of indications of association up to a point of solubles exceeding 50 % of the total asphaltenes. The-latter have implications for the further understanding and experimental investigation. of the associating nature of asphaltenes such as concentration effects during analytical characterization.     

Variation in Composition of Subfractions of Petroleum Asphaltenes

ABSTRACT

Boscan asphaltenes were precipitated from the crude oil using mixtures of toluene and heptane at temperatures of 24, 50, and 80°C. Another process of extracting solid n-heptane asphaltenes (24°C) using the same solvent systems and temperatures was also investigated. Asphaltene yield is different by the two processes at similar conditions although both increases in temperature or toluene content lead to lower solid yield. This way the asphaltene continuum was investigated from incipient flocculation to total n-heptane precipitated asphaltenes. The asphaltenes were analyzed using elemental analysis, fluorescence spectroscopy, vapor pressure osmometry, and HPLC size exclusion chromatography. The distribution of porphyrins was also measured using absor-bance spectroscopy. The asphaltenes were found to follow a regular trend in elemental ratios, H/C and N/C, indicating increased aromaticity and nitrogen content as the solid yield decreases. Also the molecular weight was seen to increase. Size exclusion chro-matograms and fluorescence spectra were found to be different comparing solids from the two separation processes. This indicates that the asphaltene fractions obtained by extraction of solid asphaltenes are altered relative to asphaltenes obtained by ordinary precipitation. The porphyrin concentration was found to diminish rapidly with solid yield decrease in both precipitation and extraction experiments, the latter fractions, however, containing significantly less asphaltenes indicating an adsorption step in the coprecipitation of porphyrins. Soluble fractions were found to exhibit relatively low molecular weights and an apparent lack of indications of association up to a point of solubles exceeding 50 % of the total asphaltenes. The-latter have implications for the further understanding and experimental investigation. of the associating nature of asphaltenes such as concentration effects during analytical characterization.     

A novel test method for evaluate asphaltene inhibitor efficiency on reservoir rock

Asphaltene deposits can reduce the productivity of the reservoir as well as foul piping and surface equipment. Current chemical and mechanical methods for treating deposition are only partially effective partly because the deposition process is poorly understood. The most commonly way to asphaltene precipitation reduction is applying an asphaltene inhibitor. In order to investigate the extent of formation damage by asphaltenes in crude oil this work has used electro kinetic technique to study the adsorption of asphaltenes in rock pores. Most researchers investigate the kinetics of adsorption by monitoring changes in the concentration of asphaltene or polymer in a dispersion of adsorbent particles or capillaries. This study is a coherent approach to measure amount of asphaltene adsorption on rock surface and survey effect of asphaltene inhibitors on precipitation reduction in porous media.     

Test Methods for Determining Asphaltene Stability in Crude Oils

Abstract

The high cost of remediating asphaltene deposition in crude oil production and processing has necessitated the development of test methods for determining the stability of asphaltenes in crude oils. In the current work, the stability of asphaltenes in crude oils of varying API gravity is predicted using the Oliensis Spot Test, the Colloidal Instability Index, the Asphaltene–Resin ratio, and a solvent titration method with NIR solids detection. The test methods are described in detail and experimental data from them presented. The experimental stability data were validated via correlation with field deposition data. The effectiveness of the various tests as predictors of the stability of asphaltenes in oils is discussed. The Colloidal Instability Index and the solvent titration method were found to predict a crude oil's propensity towards asphaltene precipitation better than both the Asphaltene–Resin ratio and the Oliensis Spot Test. For oils with low asphaltene content where most stability tests fail, live oil depressurization is proposed as the test for predicting the stability of asphaltenes.     

An Experimental Calculation of Asphaltene Critical Properties in Crude Oil Reservoir Systems

High-molecular-weight hydrocarbons and asphaltenes are important constituents of petroleum and can cause problems related to crystallization and deposition of asphaltene. This article introduces an extension of the cubic equation of state (Peng-Robinson EOS) to describe asphaltene–toluene mixture vapor–liquid equilibria (VLE) and characterize pure asphaltene, and the critical properties of asphaltene were adjusted. Experimental data were used to examine the proposed procedure in an Iranian crude oil reservoir.

We determined the critical properties of asphaltene for this EOS using a two-phase vapor–liquid equilibrium calculation. The test results showed that the proposed procedure is adequate for predicting asphaltene precipitation data.     

无机盐与沥青质的协同作用对油藏润湿性的影响

选用两种原油沥青质样品,对沥青质在岩石孔隙表面吸附所引起的润湿性改变进行了实验研究。测定结果表明,岩样润湿性改变的程度主要与沥青质的来源和岩样所含盐水的组成有关。盐水中无机阳离子的类型对沥青质所引起的油藏岩石润湿性改变有十分重要的作用。在浓度相同的情况下,阳离子价数越高,对润湿性的影响越大。盐水中的无机阴离子对沥青质引起的润湿性改变影响很小。在油气开采过程中,地层水和注入水的离子组成,特别是所含阳离子的类型,是影响油藏岩石润湿状态的一个不可忽视的因素。     

Analyzing electrical field effect on asphaltene deposition

Asphaltenes are the heaviest and most complicated fraction in a crude oil sample and consist of condensed polynuclear aromatics, small amounts of heteroatoms (e.g., S, N, and O), and some traces of metal elements (e.g., nickel and vanadium). The main mechanisms of asphaltene deposition are precipitation (formation of asphaltene solids out of liquid phase), aggregation (formation of larger asphaltene particles), and deposition (adsorption and adhesion onto the surface). Asphaltene deposition is a major unresolved flow assurance problem in the petroleum industry, which may occur anywhere in the production system consists of reservoir, wellbore, through flowing and the separator. Asphaltene moieties in crude oil are found to carry residual surface electric charge, so by exerting an electrical field in a specific length of pipe, asphaltenes will deposit and we will have no blockage problem. Determining asphaltene electric charge is an important issue that will be done by static experiment, and then effect of electrical field on asphaltene deposition in dynamic state should be investigated. This paper discusses electric field effect on asphaltene deposition and represents a way to deposit asphaltene moieties in specific location.     

Development of an Artificial Neural Network Algorithm for the Prediction of Asphaltene Precipitation

Abstract

The precipitation and deposition of crude oil polar fractions such as asphaltenes in petroleum reservoirs considerably reduce rock permeability and oil recovery. Therefore, it is of great importance to determine how and how much the asphaltenes precipitate as a function of pressure, temperature, and liquid phase composition. The authors designed and applied an Artificial Neural Network (ANN) model to predict the amount of asphaltene precipitation at a given operating condition. Among this training, the back-propagation learning algorithm with different training methods was used. The most suitable algorithm with an appropriate number of neurons in the hidden layer, which provides the minimum error, was found to be the Levenberg-Marquardt (LM) algorithm. An extensive experimental data for the amount of asphaltene precipitation at various temperatures (293–343 K) was used to create the input and target data for generating the ANN model. The predicted results of asphaltene precipitation from the ANN model was also compared with the results of proposed scaling equations in the literature. The results revealed that scaling equations cannot predict the amount of asphaltene precipitation adequately. With an acceptable quantitative and qualitative agreement between experimental data and predicted amount of asphaltene precipitation for all ranges of dilution ratio, solvent molecular weight and temperature was obtained through using ANN model.     

Mechanism of the reversibility of asphaltene precipitation in crude oil

Asphaltene precipitation and deposition occur in petroleum reservoirs as a change in pressure, temperature and liquid phase composition and reduce the oil recovery considerably. In addition to these, asphaltene precipitates may deposit in the pore spaces of reservoir rock and form plugging, which is referred to as a type of formation damage, i.e. permeability reduction. In all cases above, it is of great importance to know under which conditions the asphaltenes precipitate and to what extent precipitated asphaltenes can be re-dissolved. In other words, to what extent the process of asphaltene precipitation is reversible with respect to change in thermodynamic conditions. In present work, a series of experiments was designed and carried out to quantitatively distinguish the reversibility of asphaltene precipitation upon the change in pressure, temperature and liquid composition. Experiments were conducted in non-porous media. Generally it was observed that the asphaltene precipitation is a partial reversible process for oil under study upon temperature change with hysteresis. However, the precipitation of asphaltene as a function of mixture composition and pressure is nearly reversible with a little hysteresis.     

注气对固溶物沉淀影响的研究与应用

注气采油是提高原油采收率的主要方式之一,在此过程中准确描述含有沥青质等高分子有机固相物质的油气体系相平衡十分必要。为此,将沉淀的沥青质视为固相,假设标准状态下必须有沥青质沉淀,将标准状态压力和温度引入沥青质固相逸度计算,并同时考虑了标准状态压力和温度对沥青质固相逸度的影响,建立了能模拟沥青质沉淀的气、液、固三相相平衡热力学模型。据该模型计算的结果表明:①能通过比较液相沥青质逸度和固相沥青质逸度大小来判断固相沥青质沉淀的出现。②当注入某油的气体为烃类混合气体时,烃类混合气体的添加使得含沥青质原油的组分发生变化;温度相同时,注气浓度越高,沉淀的压力越大;浓度相同时,温度越低,沉淀的压力越大;当沉淀量一定时,随着注气浓度增加,油品的饱和压力随之增大;相同注气浓度下,当压力高于饱和压力时,随着压力增大,沉淀量减少。③在温度不变的情况下,注入某油的气体为CO2时,其沥青质沉淀量是注CO2浓度的函数且随着CO2浓度的增加,固相(沥青质)的沉淀量不断增大。④在注气驱油过程中,气体的注入极易引发含沥青质原油中沥青质等重质有机物的沉积。     

Modeling of Asphaltene Phase Behavior with the SAFT Equation of State

Abstract

The SAFT equation of state was used to model asphaltene phase behavior in a model live oil and a recombined oil under reservoir conditions. The equation of state parameters for the asphaltenes were fit to precipitation data from oil titrations with n-alkanes at ambient conditions. The SAFT model was then used to predict the asphaltene stability boundaries in the live oils. A lumping scheme that divides the recombined oil into six pseudo-components based on composition, saturates–aromatics–resins–asphaltenes fractionation, and gas–oil-ratio data was introduced. Using this lumping scheme, SAFT predicted stock-tank oil and recombined oil densities that are in excellent agreement with experiment data. For both the model and the recombined oil systems, SAFT predicted asphaltene instability and bubble points agree well with experimental measurements.     

Test Methods for Determining Asphaltene Stability in Crude Oils

The high cost of remediating asphaltene deposition in crude oil production and processing has necessitated the development of test methods for determining the stability of asphaltenes in crude oils. In the current work, the stability of asphaltenes in crude oils of varying API gravity is predicted using the Oliensis Spot Test, the Colloidal Instability Index, the Asphaltene-Resin ratio, and a solvent titration method with NIR solids detection. The test methods are described in detail and experimental data from them presented. The experimental stability data were validated via correlation with field deposition data. The effectiveness of the various tests as predictors of the stability of asphaltenes in oils is discussed. The Colloidal Instability Index and the solvent titration method were found to predict a crude oil's propensity towards asphaltene precipitation better than both the Asphaltene-Resin ratio and the Oliensis Spot Test. For oils with low asphaltene content where most stability tests fail, live oil depressurization is proposed as the test for predicting the stability of asphaltenes.     

REVERSIBILITY AND INHIBITION OF ASPHALTENE PRECIPITATION IN BRAZILIAN CRUDE OILS

ABSTRACT

A fundamental understanding of the aggregation and precipitation of asphaltenes in petroleum crudes is important for the development of preventive and curative measures for the potential problem of asphaltene deposition occurring during production, transport and refining operations. The question of reversibility of asphaltene precipitation, yet a controversial issue, is crucial for a clear and unequivocal understanding of the precipitation phenomenon, development of mathematical models that describe the behavior of asphaltenes in petroleum fluids, and the design of inhibitors. In this work, the behavior of precipitated asphaltenes in Brazilian crude tank oil samples following flocculant removal and gradual addition of fresh oil was investigated. The results obtained revealed a re-dissolution of precipitated asphaltene particles following flocculant removal and oil addition. On the inhibition of asphaltene precipitation, the capacity of a number of surfactants and block copolymers to inhibit asphaltene precipitation and deposition was also examined. Ethoxylated Nonylphenols and Hexadecyl Trimethyl Ammonium Bromide displayed highest capacity in the inhibition of asphaltene deposition.     

Study of Asphaltene Precipitation Using Refractive Index Measurement

Abstract

The measurements of the refractive index of crude oils were utilized in this work to enhance the understanding of the behavior of asphaltenes in crude oil, specifically, their tendency to precipitate from crude oil. The onset of asphaltene precipitation was measured in eight crude oil samples, which were titrated with either heptane or pentane in order to induce precipitation of the asphaltenes. The refractive index of each sample was measured to find its relationship to asphaltene precipitation. The assumption that refractive index of a mixture is a linear combination of the refractive indexes of the individual components was verified. It was also found that mixtures of heptane or pentane and crude oil also followed this same behavior. However, as asphaltenes began to precipitate from the solution, the refractive index no longer followed this linear mixing rule. Careful analysis of the refractive index data for each of the crude oil samples revealed many interesting relationships between the refractive index data and the content of the different polar asphaltene fractions present. The refractive index of asphaltenes was predicted from the refractive index data of crude oils. The results suggest the possibility predicting the properties and characteristics of the asphaltenes contained in a crude oil simply by measuring the refractive index.     

ADSORPTION OF ASPHALTENE FUNTIONALITIES AND ASPHALTENE ON GOETHTTE

ABSTRACT

Solid-stabilized water-in-oil emulsions cause many problems such as oil loss, fouling of a processing unit, and environmental hazard in the petroleum production and refining. The ability of finely divided solids to stabilize these emulsions is due to the adsorption of asphaltenes and other heavy constituents. This study presents the individual and competitive adsorption of asphaltene functionalities in cyclohexane solution and asphaltene in heptol solution onto goethite (FeOOH) particle surfaces at 25 °C to quantitatively understand the FeOOH particle-fluid interactions. The functionalities used were carboxylic acid (represented by benzoic acid), sulfoxide (by diphenylsulfoxide), and pyrrolic (by indole). The single component adsorption of these functionalities was well represented by both the Langmuir and Freundlich models, showing that adsorptive affinity for FeOOH increased in the order of indole < diphenylsulfoxide < benzoic acid. This observation was supported by the results of bi-component competitive adsorption of three functionality pairs on FeOOH, which were interpreted by the Fritz model. The adsorption of asphaltene was performed using dry and moist FeOOH surfaces and well represented by both the Langmuir and Freundlich models. The moist FeOOH yielded a decrease in the adsorption of asphaltene compared to adsorption on dry FeOOH.     

原油沥青质在油藏岩石表面的吸附特性

选用两种原油沥青质样品，对沥青质在岩石孔隙表面的吸附及吸附所引起的润湿性变化进行了实验研究。对润湿性的测定结果表明，油藏岩石润湿性改变的程度主要取决于沥青质的来源和地层水的离子组成，同时也与离子浓度和岩样的束缚水饱和度有关。通过使用分光光度法测定沥青质在砂岩上的吸附量，初步建立了润湿指数（ＷＲ）与沥青质吸附量（ａ）之间的定量关系。对于某一给定的原油沥青质，ＷＲ值随ａ值增加而趋于降低。图４表３参１０（邓春萍摘