Patent Application
20210356416
The present invention is in relation to a method and its apparatus, to be used for continuous monitoring of hydrogen chloride (HCl) generation from hydrolysis reactions or thermal decomposition of chloride salts. Such reactions occur at temperatures typically found during oil distillation, and which are undesirable, as HCl causes corrosion and salt deposits in fractionating columns. The invention allows for a much more sophisticated and precise record of the thermal events brought about as a function of temperature. It also allows the behavior of chloride salts subjected to these conditions to be evaluated, both in model systems and in industrial saline solutions, with respect to the respective content, composition, or presence of components in the oil phase, such as carboxylic (naphthenic acids) or nitrogenous (ammonia or amines) acids.
Chloride salts are, in general, very poorly soluble in oil, being dragged to the fractionation tower in emulsified water droplets. With the exception of petroleum carboxylic acids (naphthenic acids), little or no participation of the hydrocarbon matrix in the reactions is expected, except as a thermal fluid. The rate of HCl generation during distillation therefore depends heavily on the composition of this emulsified aqueous solution and on the temperature. With that in mind, Eaton and colleagues (2005) set up a laboratory inspired by Davis and colleagues (L L Davis, J. M. Jones, and C. A. Neilson, “Laboratory Control of Corrosion of Distillation Equipment and Desalting Processes,” Oil and Gas Journal, 37, No. 2, 62 (1938)) where petroleum or paraffin oil with a high boiling point, containing different levels of sodium chloride, magnesium chloride and calcium chloride, are heated to 350° C.
There were other publications in 2008 and 2009 (M. R. Gray, P. E. Eaton, T. Le, “Kinetics of Hydrolysis of Chloride Salts in Model Crude Oil,” Petroleum Science and Technology, v. 26, pp. 1924-1933, 2008; Y. Londono, R. Mikula, P. Eaton, M. R. Gray, “Interaction of Chloride Salts and Kaolin Clay in the Hydrolysis of Emulsified Chloride Salts at 200-350° C.,” Petroleum Science and Technology, v. 27, pp. 1163-1174, 2009). In these publications, a method is described in which, during temperature programming, the salt-containing fluid is continuously purged by steam. A downstream condensation system condenses steam and HCl that derives from the fluid at a certain temperature, the chloride content being determined by ion chromatography in the condensed water. Once the outflow of steam and the temperature in the flask are known, the HCl evolution curve is derived as a function of temperature.
However, this type of configuration makes it impossible to continuously monitor the evolution of chloride, since it is necessary to accumulate condensed water. Important information is therefore lost, such as the instantaneous rate of HCl generation as a function of temperature. The publications also do not mention the determination of ammonium chloride (NH4Cl) on the top of the apparatus.
The formation of NH4Cl deposits inside fractionating columns can be extremely harmful to the operation and the integrity of the equipment. The tendency for NH4Cl, to accumulate the formation of which is largely dependent on the composition of droplets from the aqueous phase emulsified in oil, is essential information in predicting possible complications during distillation.
Oil distillation units may be subject to corrosion and salt deposits. Both processes generally occur in the upper section and on top of fractionating columns, where there is condensation of light hydrocarbons and steam. The origin of the corrosion is mainly linked to hydrogen chloride (HCl), an acidic gas that is produced in the hotter regions of the fractionators, from chloride salts present in oil. At the top of the column, HCl may either dissolve in condensed water and form hydrochloric acid, which causes acid corrosion, or it may react with ammonia (NH3) and produce NH4Cl, a solid that causes under-deposit corrosion.
The reactions that give rise to HCl are generically known as hydrolysis and result from the reaction between certain chloride salts with steam:
MeClx+xH2O→Me(OH)x+xHCl
where MeClx is, for example, magnesium chloride (MgCl2) or calcium chloride (CaCl2). In the case of magnesium chloride, hydrolysis may also occur due to decomposition of the hydrated salt (MgCl2.6H2O), which occurs after vaporization of the emulsified water droplets.
These reactions typically occur starting at 250° C. However, other chloride salts that might be in the oil can produce HCl when heated, even in the absence of water. Examples of these salts are ammonium chloride (NH4Cl) or amines, which decompose thermally at the temperatures at the bottom of a distillation column:
R3NHCl→R3N+HCl
where R can be a hydrogen atom or an alkyl or aryl radical.
In general, therefore, the less efficient the desalting of an oil, the more intense HCl generation must be during its distillation, and the greater the acidity and chloride content of the water on the surface. However, the way in which the different chloride counterions (Na+, Mg2+, Ca+2, NH4+, etc.) are distributed is also of paramount importance.
Industry experience shows that different oils, when distilled, have different HCl evolution rates. The intensity with which a given oil generates HCl is evaluated from the pH and the chloride content in the condensed water at the top of the distillation. It may also be inferred from the chloride content in the oil prior to distillation, which typically must be lower than 5 mg/kg.
Although these determinations are useful for monitoring of the unit, and they generate information regarding processing, these parameters do not allow the potential for HCl evolution of a given oil shipment to be anticipated. It is therefore necessary to have a way to determine the potential HCl generation of an oil when it is distilled, so that a refinery will be able to project the behavior of a shipment.
Patent PI11004231 discloses a process and system for extracting salts from crude oil, specifically light and heavy oils. Specifically, the invention reveals an extraction of salts in oil with constant heating and boiling for specific periods of time. The extraction of the salts occurs via solvents contained in the oil and analysis is performed by potentiometric titration.
Document PI11005360 discloses a process for extracting salts from crude oil, specifically light oils. In particular, the invention describes the extraction of petroleum salts by means of mechanical stirring and without constant heating. More specifically, the invention comprises an extraction of salts via solvents added to the oil, followed by analysis using potentiometric titration. For the extraction process, an Erlenmeyer flask and a magnetic stirrer (mechanical stirring using a magnetic bar) are used. The oil/solvent mixture is previously heated to facilitate the mixing process.
U.S. Pat. No. 6,902,662 discloses a method for reducing the hydrolysis of chlorinated compounds contained in hydrocarbon fractions. Hydrolysis occurs at elevated temperatures and in the presence of water, forming hydrochloric acid. Hydrochloric acid is neutralized by a treatment agent composed of at least one complex oxide or metal carbonate with an organic acid dispersing agent. The treatment agent is introduced into the hydrocarbon stream between the desalter and the oven, in a place where the temperature is lower than that of the hydrolysis of chloride salts.
The document “FORTUNY, M. et al. “Measuring salinity in crude oils: Evaluation of methods and improved procedure,” Fuel, v. 87, pp. 1241-1248, 2008, reveals a procedure developed to determine the amount of salts present in crude oils for which the available laboratory techniques are unable to provide accurate salt content values. The technique is based on mixing water with crude oil by stirring, forming an emulsion. Then water is separated by microwave energy irradiation for several minutes. This three-step process involves emulsification of the salt-free washing water into crude oil, followed by recovery of the water by microwave heating, and finally, analysis of the salt content using the classic Mohr titration method.
The document “MORIGAKI, M. K. et al. “Salinidade em Petróleo Bruto: Otimização de Metodologia e Proposta de um Novo Método para Extração de Sais em Petróleo, Quimica Nova” [Salinity in Crude Oil: Optimization of Methodology and Proposal of a New Method to Extract Salts from Petroleum], Quimica Nova, v. 33, pp. 607-612, 2010, presents a study to implement changes to improve the ASTM D 6470 method and a new methodology for extracting salts using a mechanical stirring process without heating. The results from optimization produce greater efficiency and safety in the process, compared to the traditional ASTM method.
It is therefore important to emphasize that there are methods for measuring salts in crude oil, but none continuously monitor HCl generation due to hydrolysis reactions or thermal decomposition of chloride salts as the present invention does.
By continuously monitoring HCl generation, the method of the present invention allows for a sophisticated and precise record of thermal events that occur during oil distillation, allowing the behavior of model systems or industrial saline solutions to be predicted, both in terms of content or composition of chloride salts, in regard to the influence of nitrogenous components (ammonia or amines) or carboxylic acids (naphthenic acids).
The present invention is used to evaluate the composition of industrial saline solutions on the evolution of HCl, NH4Cl and amine chloride during oil distillation, contributing to the prevention of production losses resulting from equipment replacement and cleaning of fractionating columns, in addition to assisting in the optimal allocation of oil in a group of refineries.
The present invention also allows the composition of industrial saline solutions on the evolution of HCl, NH4Cl and amine chloride during the distillation of oil to be evaluated, reducing the possibility of serious issues, such as the appearance of holes in fractionating columns and in related equipment resulting from uncontrolled corrosion, which can lead to loss of liquid containment and fires in refineries.
In addition, the present invention also makes it possible to evaluate the composition of industrial saline solutions on the evolution of HCl, NH4Cl and amine chloride during oil distillation, resulting in maximization of the campaign time of fractionating columns and related equipment.
The present invention is in relation to a method and its apparatus for continuous monitoring of HCl generation, resulting from hydrolysis reactions or thermal decomposition of chloride salts. The system provides an accurate record of the thermal events that occur during oil distillation, thus allowing the behavior of model systems or industrial saline solutions to be predicted, both with respect to the content of chloride salts, and the influence of nitrogenous components (ammonia or amines) or carboxylic acids (naphthenic acids).
The invention is applicable in the prior assessment of the aggressiveness of petroleum with regard to HCl generation and the deposit of solids, such as ammonium chloride or amine chlorides, thus contributing to the integrity and reliability of oil fractionating columns and respective top systems.
The invention is also applicable to the research and development of factors related to the composition and temperature of chloride evolution in petroleum distillation conditions, as well as to the study of additives that are able to mitigate HCl evolution.
The present invention will be described in more detail below, referencing the attached figures which, schematically and in a manner that is not limiting on the inventive scope, show examples of the invention's embodiments. The drawings are as follows:
The present invention deals with a method and its apparatus for continuous monitoring of HCl generation, resulting from hydrolysis reactions or thermal decomposition of chloride salts.
Hydrolysis or thermal decomposition occurs in a flask containing paraffin oil, to which a known mass of chloride salts, pure and/or dissolved in water has been added. The mixture is stirred throughout the entire test and heated according to a certain temperature ramp.
As the temperature of the paraffin oil rises, the hydrogen chloride generated in the flask is continuously dragged by the flow of an inert gas (nitrogen or helium, for example). The gas flow containing HCl is bubbled in water, contained in a flask for potentiometric titration. Hydrogen chloride is instantly absorbed, which causes a variation in the electrochemical potential of the medium. The variation is perceived by an appropriate sensor (electrode), which automatically sends the information to a potentiometric titrator. The titrator adds a titrant solution (standardized solution of AgNO3, NaOH or KOH, for example) in order to bring the electrochemical potential back to its original value. This process is repeated continuously throughout the test, until it is finished at the discretion of the operator or until the hydrolysis reactions or thermal decomposition of chloride salts are exhausted.
Data on the temperature of the paraffin oil, the electrochemical potential of the solution, and the volume of titrant are transmitted to a computer, which is also responsible for controlling the potentiometric titrator and processing the information. The titrant consumption corresponds to a certain mass of HCl that reaches the titration flask, which in turn occurs at a certain time following the start of the test, and at a certain temperature of the paraffin oil. In the end there are curves that plot the HCl generation rate and the total HCl generated as a function of time and temperature.
The present invention also reveals the apparatus, as well as its method of assembly, for evaluating hydrogen chloride as a function of temperature.
The apparatus consists of the following components:
The method of assembling the apparatus is described below:
The method for acquiring HCl evolution data comprises the following steps:
The following tests were carried out for this study, which are examples of embodiments of the present invention.
117.2 mg of 4-nitro-anilinium chloride were added to 1,095 kg of chloride-free vacuum-hydrogenated gasoil (paraffin oil) contained in a three-way flask, which was heated according to the following temperature curve:
i. 35° C., for 2 minutes;
ii. 35° C. to 120° C., in 72 minutes;
iii. 120° C., for 180 minutes (isothermal).
Along the entire heating curve, N2 was bubbled into the paraffin oil at a flow rate of 180 mL/min. The gas flow was conducted to a flask containing 190 mL of water, whose electrochemical potential was adjusted to 20 mV. At each displacement of the initial electrochemical potential, resulting from the introduction of HCl into the flask, an AgNO3 solution with a concentration of 0.1 mol/L was added by an automatic titrator until the return to the initially adjusted electrochemical potential.
Finally, the titrant consumption curve, and consequently the evolution of HCl over the temperature program, are obtained. As can be seen in
76.6 mg of sodium chloride (NaCl), 37.1 mg of calcium chloride dihydrate (CaCl2.2H2O) and 24.6 mg of magnesium chloride hexahydrate (MgCl2.6H2O) were diluted in 5 mL of deionized water. This solution was transferred to a round-bottom flask containing 900 g of synthetic lubricating oil (paraffin oil).
The following temperature program was used:
Along the entire heating curve, N2 was bubbled into the paraffin oil at a flow rate of 180 mL/min. Because an aqueous solution was added to the paraffin oil in this example, and not a pure substance, the line that leads the flow of N2 containing HCl to the flask where the titration occurs was kept at 150° C. to prevent water condensation. The electrochemical potential of the water where HCl is absorbed and titrated with AgNO3 with a concentration of 0.01 mol/L was adjusted to 29.8 mV. With each displacement of the initial electrochemical potential resulting from introduction of HCl into the flask, titrant is added by an automatic titrator until the return to the initial electrochemical potential.
Finally, the titrant consumption curve is obtained, and consequently the evolution of HCl over the temperature program. As shown in
5 ml of industrial saline solution was added to the same paraffin oil in Example 2, containing 120 mg/L sodium, 26 mg/L calcium, 5.5 mg/L magnesium, 610 mg/L chloride and 129 mg/L nitrogen. The same temperature program as that used with the paraffin oil and the transfer line to the titration flask was used. HCl evolution intensified from 110° C. and at the end reached 11%, as seen in
Note that although the present invention has been described in relation to the attached drawings, it may undergo modifications and adaptations by technicians versed in the subject, depending on the specific situation, but as long as it is within the inventive scope defined herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| BR 102020009844-6 | May 2020 | BR | national |
