Erland L. Nordgård

Behavior of Asphaltene Model Compounds at W/O Interfaces

Asphaltenes, present in significant amounts in heavy crude oil, contains subfractions capable of stabilizing water-in-oil emulsions. Still, the composition of these subfractions is not known in detail, and the actual mechanism behind emulsion stability is dependent on perceived interfacial concentrations and compositions. This study aims at utilizing polyaromatic surfactants which contains an acidic moiety as model compounds for the surface-active subfraction of asphaltenes. A modified pulse-field gradient (PFG) NMR method has been used to study droplet sizes and stability of emulsions prepared with asphaltene model compounds. The method has been compared to the standard microscopy droplet counting method. Arithmetic and volumetric mean droplet sizes as a function of surfactant concentration and water content clearly showed that the interfacial area was dependent on the available surfactant at the emulsion interface. Adsorption of the model compounds onto hydrophilic silica has been investigated by UV depletion, and minor differences in the chemical structure of the model compounds caused significant differences in the affinity toward this highly polar surface. The cross-sectional areas obtained have been compared to areas from the surface-to-volume ratio found by NMR and gave similar results for one of the two model compounds. The mean molecular area for this compound suggested a tilted geometry of the aromatic core with respect to the interface, which has also been proposed for real asphaltenic samples. The film behavior was further investigated using a liquid-liquid Langmuir trough supporting the ability to form stable interfacial films. This study supports that acidic, or strong hydrogen-bonding fractions, can promote stable water-in-oil emulsion. The use of model compounds opens up for studying emulsion behavior and demulsifier efficiency based on true interfacial concentrations rather than perceived interfaces.

Model Compounds for Asphaltenes and C80 Isoprenoid Tetraacids. Part I: Synthesis and Interfacial Activities

Three model compounds for asphaltenes and two model compounds for the C80 isoprenoid tetraacids (ARN) have been synthesized and their interfacial and solubility properties were investigated. All compounds exhibit high interfacial activities. The asphaltene models lowered the interfacial tension between toluene and pH 9 to around 5 mN/m at 12.5–35 μM and the tetraacid models gave a drop in the interfacial tension between chloroform and pH 9 to 13 mN/m at only 5 μM, which is consistent with previous findings for the natural occurring C80 tetraacids. A sudden drop in the IFT over a very narrow concentration range was observed for two of three asphaltene models. NIR spectroscopy studies indicated an aggregation most likely a result of polar and hydrogen bond interactions. The IFT results also showed different behavior with only small changes in chemical structure. The tetraacid models have similar interfacial behavior as the C80 tetraacids and will thus be suitable model compounds with their highly UV active and fluorescent properties.

Determination of C80 tetra-acid content in calcium naphthenate deposits

A method is described which allows to determine the content of the so-called C(80) tetra-acid molecules (TA) in calcium naphthenate deposits. The method consists of four steps. Molecules present in the deposit are dissolved in a mixture of toluene and 2-butanol after an acidic treatment. All acid molecules are then selectively extracted and concentrated by a solid-phase extraction (SPE) method. After derivatization of acids into their naphthacyl esters to increase the sensitivity of the detection, TA is separated and detected by reversed-phase HPLC with UV detection. We have checked that all the steps are quantitative and the method appears selective. The TA content can be determined in presence of other naphthenic acids. Using this methodology we have determined the TA content in three calcium naphthenate deposits from different oil fields. It appears that these deposits have a similar TA concentration between 28 and 41% (w/w).

Interfacial Shear Rheology of Calcium Naphthenate at the Oil/Water Interface and the Influence of pH, Calcium, and in Presence of a Model Monoacid

In this article, the interfacial shear rheological properties of calcium naphthenate with a model tetraacid at the chloroform/xylene-water interface has been investigated as a function of aqueous pH, calcium concentration and monoacid concentration. The experiments are carried out using an interfacial rheology system with an electro commutated motor, direct strain oscillation and a biconical bob geometry. The model tetraacid used, BP10, has previously been shown to have similar bulk and interfacial properties as a narrow group of tetraprotic, so-called Arn acids, and these acids are known to be responsible for formation of hard deposits during oil recovery. A great increase in the elastic modulus was observed around pH 6.2, which is in agreement with observations from oil fields with calcium naphthenate deposition problems. The gel strength and elastic nature is highest around the gelation onset, believed to be due to a bilayer-like conformation of the tetraacid generating a densely packed interface with high cross-linking density and possible film growth. As a function of calcium concentration, both a reduction of the gel strength and slower gel formation was observed when decreasing the calcium concentration from 10 to 4 mM. Myristic acid, a linear C14 fatty acid, was employed as a model for indigenous monoacids and the influence onto the viscoelastic properties of the Ca2+-TA film was studied as a function of myristic acid concentration at pH 8.0 and 6.5. A great reduction of both the gel strength and elasticity was obvious in the range of 100 to 1000 higher monoacid than tetraacid concentration. This is however typical indigenous acid concentrations for an acidic crude oil, and may indicate that indigenous monoacids have the ability to act as indigenous inhibitors towards formation of calcium naphthenate. This could explain why some Arn-containing acidic crude oils have deposition problems while others do not. Moreover, all parameters should be taken into account when predicting the deposition risk for a given crude oil, such as concentrations of Ca2+, Arn, monoacids and other indigenous acids.

Potentiometric Titrations of Five Synthetic Tetraacids as Models for Indigenous C80 Tetraacids

The acid/base properties, critical micelle concentrations (cmcs), and pH-dependent solubility of five synthetic tetraacids have been studied at several ionic strengths (20-600 mM NaCl) and in the pH range of 1.5-11 using high precision potentiometric titrations, tensiometer measurements, and UV spectroscopy, respectively. The molecular weight of the tetraacids ranged between 478 and 983 g/mol. The potentiometric titration data was evaluated in terms of thermodynamic equilibrium models, developed in the light of relevant solubility data, Langmuir monolayer compressions and cmc of the different tetraacids. The results indicate that for two of the tetraacids, called BP5 and BP7, two chemical forms fully dominate the speciation of the monomers; the insoluble fully protonated form, and the soluble fully deprotonated form. The partly protonated species, only play a very minor role in the speciation of these tetraacids. For the other tetraacids the results are more complicated; for the smallest tetraacid, called BP1, all species seem to play important roles, and for the most hydrophobic, BP10, the formation of micelles and aggregates severely complicates the evaluation of the speciation. For the tetraacid BP3 one of the partly deprotonated forms seems to be important, thus confirming the structure to properties relationship. In spite of the complicated micelle formation chemistry, and although not actually measured, the acid/base properties for the monomers of BP10 were interpreted by means of surface charge densities of the micellar aggregates. The modeling indicates an increase of the aggregation number of the micelle upon acidification, a result of formation of mixed micelles incorporating the fully protonated and deprotonated species. An intrinsic pK(a) of 5.4 for BP5 was used to model the monomer pK(a) of BP10, and corresponded well with a monolayer acidity constant pK(s)(a) of 5.5 obtained from surface collapse pressures of Langmuir monolayers as a function of pH.

Aggregation of tetrameric acids in aqueous media studied by small-angle neutron scattering

This article presents the characterization of two self-associated structures, a C(80)-tetraacid (also known as ARN), which is an aliphatic molecule present in crude oil and responsible for the formation of deposits, and BP-10, a molecule designed to model the properties of the C(80)-tetraacid. These molecules have four carboxylic functions at the end of four interconnected hydrocarbon chains and can be dissolved in aqueous solution and in basic media. In this paper we have used small-angle neutron scattering (SANS) as the main method to study the tetrameric acids in solution. SANS measurements show that the two molecules (in sodium form) exhibit very different types of aggregation properties in aqueous solution. More specifically, Na(4)BP-10 forms nanometer-sized micelles with an aggregation number close to 5 (at concentrations above the critical micellar concentration) in both 20 mM NaCl and 0.9 wt.% 1-butanol media. On the contrary fully ionised C(80)-TA forms very large structures in pure D(2)O and NaCl 20 mM, so large that their exact dimensions could not be determined by SANS.

Oil-Water Partitioning of a Synthetic Tetracarboxylic Acid as a Function of pH

The oil-water partitioning of a synthetic tetraacid acting as a model compound for indigenous C80-C82 ARN acids has been studied as a function of pH, ionic strength and type of monovalent counterion. Experimental data obtained with ultraviolet-visible and HPLC/UV analyses have been fitted to thermodynamic models based on one, two or four dissociation steps to obtain o/w partition coefficients (K wo ) of the fully protonated acid between chloroform and aqueous solutions, and its apparent acidity constant(s), pK a. As the study is conducted above the CMC of the tetraacid, in general high apparent acidity constants were obtained in the range from 6 to 8 resulting from micellization equilibria. K wo values were obtained in the range from 10−3 to 10−4, and decreasing with increasing salinity. At 50 mM K+, no conclusions could be made regarding the number of distinguishable dissociation steps, while at higher ionic strength (184 mM and 452 mM K+) and at 184 mM Na+ a model with two dissociation steps provided good fits to the experimental data. The first step was found to be given by a pK a ≈ 6.6–6.8 and the second dissociation step at pK a values ≈ 7.8–8.3. The two-step mechanism supports previous results obtained by potentiometric titrations. No significant difference in the o/w behavior was observed when changing the counterion from potassium to sodium. The main partitioning of the tetraacid in the aqueous phase occurred above pH 8, where the fully deprotonated acid was formed.

Inhibition of Calcium Naphthenate. Experimental Methods to Study the Effect of Commercially Available Naphthenate Inhibitors

In this study, different methods have been developed for studying naphthenate inhibitors. One first method is based on interfacial activity of systems with naphthenic acids, inhibitors, and calcium viewing reaction mechanisms at interfaces of the inhibitors. A second method is based on gravimetrical determination of interfacial layer in a two phase system and gives a thermodynamic approach to naphthenate formation, and a third method utilizes a ultraviolet-active model tetraacid to directly determine the depletion in bulk phase concentration during a two-phase reaction. The results indicate that inhibitors may act through several mechanisms, and depending on the total system different mechanisms may have the highest efficiency also by combining several mechanisms.

Methods to Study Naphthenate Formation in w/o Emulsions by the Use of a Tetraacid Model Compound

Precipitation of naphthenate salts is normally a problem in the processing of acidic crude oils. In this study, the goal was to find suitable methods to investigate the interfacial reaction between tetraacid and calcium under emulsified conditions. Two different systems have been studied depending on composition and applied shear. The influence of inhibitors has been investigated and the same inhibitor was found to be the most effective one regardless of the system. Depletion of tetraacid in the oil phase was analyzed with UV-vis and HPLC. Interfacial area and droplet size in the emulsions were measured with fluorescence microscope and pulse-field gradient NMR. Since this reaction takes place over the interface, the investigation clearly documents, the importance of the total interfacial area of the emulsified system.