This disclosure generally relates to inhibiting corrosion in liquid hydrocarbon facilities and, in particular, detecting the onset of salt formation in overhead fluid systems and inhibiting said salt formation.
In a hydrocarbon refinery, a crude unit may clean oil through water washing in a desalter and then split the oil into fractions in an atmospheric distillation tower. These fractions are pumped to various processing units downstream of the crude unit (e.g., coker, catalytic cracker, hydrotreater etc.). When leaving the distillation tower, the hydrocarbons may travel through an overhead fluid system. Acids contained in these fractions may undesirably cause corrosion in the overhead systems. These acids may be conventionally neutralized with basic amine additives. Changes in environmental or chemical conditions of the hydrocarbon fluids in the overhead fluid system may lead to the formation of amine salts that may themselves cause corrosion of the overhead fluid pipe(s). These changes may also lead to the hydrocarbon fluid passing through the dew point of water contained therein. The term “dew point” refers to the point of initial condensation of steam to water or the temperature at which a phase of liquid water separates from the water vapors and liquid hydrocarbons and begins to form liquid water as the vapors cool. The liquid water may have amine salts dissolved therein which will dissolve and dissociate in the water decreasing the pH of the water to an acid pH that also contributes to corrosion of the overhead fluid piping.
Refinery crude unit processing can be challenging and complex, and most of the corrosion in overhead fluid systems may take place during periods where corrosion parameters difficult to measure and evaluate. It is not uncommon for the period between sample collection, analysis, and results reporting for an overhead fluid system to span three weeks. This lengthy period leads to some systems only being tested one to three times per calendar year. Attempts to compensate for intermittent or long period corrosion monitoring have included installing online pH meters on atmospheric distillation towers overhead accumulator water boots, however, these systems are often used to detect the formation of acids in the liquid phase of water after the fluid has passed its dew point. Since the detection methods focus on the detection of pH changes in the liquid water phase, the salt formation corrosion has already begun before the pH change is detected. Since the water in the fluid may reach its dew point in any overhead equipment, such as along the length of the overhead pipes, the pH based methods tend to only address acid based corrosion downstream of the location where the dew point occurred. Thus, there is an ongoing need for on-line and automated methods for monitoring the onset of amine salt formation to reduce corrosion in overhead fluid systems since such methods would address corrosives prior to the formation of acids and along piping segments upstream of the dew point location.
In aspects, this disclosure generally relates to inhibiting corrosion in liquid hydrocarbon facilities and, in particular, detecting the onset of salt formation in overhead fluid systems and inhibiting said salt formation.
One embodiment according to the present disclosure includes a method for estimating the onset of corrosive species formation in an overhead fluid system, comprising: estimating the onset of salt formation in the overhead fluid system using a value of at least one parameter of a fluid selected from the group consisting of: pH, temperature, pressure, composition, density, flow rate, total steam, presence or level of a compound selected from the group consisting of: chloride, total amine, total nitrogen, halogen, bromide, iodide, oxygen, water, ammonia level, methylamine, dimethylamine, ethylamine, monoethanolamine, ethylenediamine, trimethylamine, n-propylamine, isopropylamine, monomethylethanolamine, n-butylamine, sec-butylamine, tert-butylamine, isobutylamine, diethylamine, pyrrolidine, ethyldimethylamine, dimethylethanolamine, 3-methoxypropylamine, diethanolamine, dimethylisopropanolamine, methyldiethanolamine, morpholine, piperidine, cyclohexylamine, diethylethanolamine, di-n-propylamine, diisopropylamine, n-methylmorpholine, n-eththylmorpholine, di-n-butylamine, diisobutylamine, triethylamine, dimethylaminopropylamine, and combinations thereof, and combinations thereof.
Another embodiment according to the present disclosure includes a system for estimating corrosive species formation in an overhead fluid system, comprising: an array of sensors comprising: a pH sensor; a chloride sensor; a nitrogen sensor, where the nitrogen sensor is selected from a group consisting of: an ammonia sensor, a total amine sensor, a total nitrogen sensor, and combinations thereof; a processor; a memory storage device, the memory storage devices including instructions that, when executed, cause the processor to perform a method, the method comprising: estimating the onset of corrosive species formation in the overhead fluid system using a value at least one parameter of a fluid selected from the group consisting of: pH, chloride, total amine, total nitrogen, and ammonia.
Another embodiment according to the present disclosure includes a computer readable medium product having stored thereon instructions that, when executed by at least one processor, perform a method the method comprising: estimating an onset of corrosive species formation in real-time in an overhead fluid system using a value at least one parameter of a fluid where the fluid parameter is selected from the group consisting of: pH, temperature, pressure, composition, density, flow rate, total steam, presence or level of a compound selected from the group consisting of: chloride, total amine, total nitrogen, ammonia, halogen, bromide, iodide, oxygen, water, methylamine, dimethylamine, ethylamine, monoethanolamine, ethylenediamine, trimethylamine, n-propylamine, isopropylamine, monomethylethanolamine, n-butylamine, sec-butylamine, tert-butylamine, isobutylamine, diethylamine, pyrrolidine, ethyldimethylamine, dimethylethanolamine, 3-methoxypropylamine, diethanolamine, dimethylisopropanolamine, methyldiethanolamine, morpholine, piperidine, cyclohexylamine, diethylethanolamine, di-n-propylamine, diisopropylamine, n-methylmorpholine, n-eththylmorpholine, di-n-butylamine, diisobutylamine, triethylamine, dimethylaminopropylamine, and combinations thereof, and combinations thereof.
Examples of the more important features of the disclosure have been summarized rather broadly in order that the detailed description thereof that follows may be better understood and in order that the contributions they represent to the art may be appreciated.
For a detailed understanding of the present disclosure, reference should be made to the following detailed description of the embodiments, taken in conjunction with the accompanying drawings, in which like elements have been given like numerals, wherein:
The present disclosure relates to methods and systems for inhibiting corrosion in liquid hydrocarbon facilities and, in particular, detecting the onset of salt formation in overhead fluid systems and inhibiting said salt formation. Overhead fluid systems may contain one or more hydrocarbons, non-condensable gases, and water. The water may be in a liquid or vapor phase depending on the system temperature/pressure.
Corrosive species, such as salt and acids formed when salts dissolve in liquid water, are primary contributors to corrosion in hydrocarbon processing. Hence, corrosion control plays a vital role in maintaining system integrity. The present disclosure provides methods and systems for inhibiting acid and salt formation corrosion by monitoring the onset of corrosive species formation. Sensors may be used to obtain data about salt formation predictors, including, but not limited to, one or more of: pH, temperature, pressure, density, flow rate, water wash rate, total steam, hardness, presence or levels of one or more of: chloride, total amine, total nitrogen, ammonia, halogen, bromide, iodide, oxygen, water, methylamine, dimethylamine, ethylamine, monoethanolamine, ethylenediamine, trimethylamine, n-propylamine, isopropylamine, monomethylethanolamine, n-butylamine, sec-butylamine, tert-butylamine, isobutylamine, diethylamine, pyrrolidine, ethyldimethylamine, dimethylethanolamine, 3-methoxypropylamine, diethanolamine, dimethylisopropanolamine, methyldiethanolamine, morpholine, piperidine, cyclohexylamine, diethylethanolamine, di-n-propylamine, diisopropylamine, n-methylmorpholine, n-eththylmorpholine, di-n-butylamine, diisobutylamine, triethylamine, dimethylaminopropylamine, sodium, calcium, magnesium, free oxygen, iron, nickel, copper, chromium, manganese, zinc, molybdenum, titanium, and combinations thereof, and combinations thereof. While high fluid velocities do not cause corrosion, high fluid velocities may aggravate corrosion. However, water wash systems configured to prevent the onset of corrosive species may suffer reduced effectiveness if the water wash rate falls below a required minimum for a given overhead wet hydrocarbon fluid system configuration. Collectively these are fluid parameters. Also, by the term “level” is meant proportion or quantity. A value of a fluid parameter may include, but is not limited to, one of: (i) an amount, (ii) a concentration, (iii) a proportion, (iv) a ratio, and (v) a rate. By inputting the data from the sensors (along with static information such as piping parameters) into a model, the onset of salt formation may be estimated. Herein, “onset” may refer to the actual event of salt formation or a predictive future event of salt formation. The model for processing the data may include, but is not limited to, at least one of: a mathematical model and a nomograph. In some aspects, a safety margin may be proscribed between the current conditions and a known point where salt formation will occur. When operating on the safe side of the safety margin, corrosion may be markedly reduced.
Some embodiments may include sensors used to obtain acid corrosion predictors, including, but not limited to, levels of one or more of: halogens (fluoride, bromide, etc.), organic acids (formic, acetic, propionic, buteric, valeric, etc.) and sulfur species (bisulfide, sulfide, sulfate, thiosulfate, sulfite, etc.). Some embodiments may include sensors for estimating the onset of salt formation and estimating acid corrosion predictors.
Overhead fluid systems, such as those coming from a distillation unit, have highly unique and variable environments, especially in terms of temperature, pressure, and flow rates. Over the length of an overhead fluid system, while the temperature declines, the aqueous fluids and/or hydrocarbon fluids within may change phase and/or phases may drop out of the hydrocarbon process stream. Different fluids may drop out at different times and locations along the journey of the process stream through the overhead fluid system. One key location along the overhead piping may be the position where the water dew point occurs, such as in, but not limited to, overhead piping, upper sections of a distillation tower, overhead system condensing equipment, and overhead system water separation equipment. A key contributor to acidic corrosion in an overhead fluid system at the water dew point is the presence of hydrochloric acid. Sensors may be used to identify the sections of the overhead pipe where conditions are right for liquid water to condense or drop out of the process stream.
The present disclosure includes sensors positioned so that changes in parameters, such as temperature, pressure, flow rate, hydrogen permeation, resistivity of the overhead pipe, and corrosimeter probe data may be measured at multiple points along the overhead fluid system. The sensors may be positioned at various locations including the overhead and the accumulator of an overhead fluid system. Parameters that are relatively insensitive to position along the overhead fluid system may be measured at a single location. The sensors may be configured for periodic, continuous, or ad hoc operation, and a controller may be configured to apply the sensor data to the model on a periodic, continuous (real-time), or ad hoc basis. Herein, “real-time” includes sufficient monitoring continuity such that a change in the sensor data may be detected within a few seconds or a few minutes. The term “controller” refers to a manual operator or an electronic device having components such as a processor, memory device, digital storage medium, cathode ray tube, liquid crystal display, plasma display, touch screen, or other monitor, and/or other components. The controller is preferably operable for integration with one or more application-specific integrated circuits, programs, computer-executable instructions or algorithms, one or more hard-wired devices, wireless devices, and/or one or more mechanical devices. Moreover, the controller is operable to integrate the feedback, feed-forward, or predictive loop(s) of the system. Some or all of the controller system functions may be at a central location, such as a network server, for communication over a local area network, wide area network, wireless network, internet connection, microwave link, infrared link, and the like. In addition, other components such as a signal conditioner or system monitor may be included to facilitate signal transmission and signal-processing algorithms. In some embodiments, a controller may provide instructions to various components (e.g., chemical injection pumps). The controller may be automated, semi-manual, or manual. In some embodiments, the controller may receive data from the sensors real-time via a computer network.
When the onset of salt formation is estimated, the system may be configured to send an alarm to an operator. The system may also be configured to provide instructions or control parameters to inhibit salt formation. Controllable parameters may include, but are not limited to, one or more of: (i) temperature, (ii) pressure, (iii) flow rate, (iv) water wash rate, (v) total steam, (vi) amount of additive, (vii) location of additive injection and (viii) type of additive. Total steam may include the quantity of steam added to a distillation tower. Since acids may be neutralized by the introduction of amine additives and amine salts may be formed when certain amine additives are increased, there may be circumstances where amine salt formation corrosion may be increased due to efforts to neutralize acid corrosion. In some embodiments, amine salt formation may be inhibited by selecting the amine used to neutralize acid corrosion to avoid amine salt formation.
If the onset of a corrosive condition is determined, the controller 150 may send instruction to an alarm or notification system 170, an environmental regulator 180, and/or an additive/chemical regulator 190. The environmental regulator 180 may be configured to alter one or more of the pressure, temperature, flow rate, water wash rate, or phase of the process stream. In some embodiments, environmental regulator 180 may include one or more of: (i) a temperature regulator, (ii) a pressure regulator, (iii) a flow regulator, and (iv) a water wash regulator. The additive regulator 190 may be configured to inject estimated amounts and/or types of additive to the process stream to inhibit salt formation. Additives may be added to the process stream at any point along the process stream, including, but not limited to, one or more of: the overhead fluid system piping and the tower feed stream. Additives that may be injected to inhibit acid corrosion may include, but are not limited to, one or more of: water, sodium hydroxide, potassium hydroxide, lithium hydroxide, methylamine, dimethylamine, ethylamine, monoethanolamine, ethylenediamine, trimethylamine, n-propylamine, isopropylamine, monomethylethanolamine, n-butylamine, sec-butylamine, tert-butylamine, isobutylamine, diethylamine, pyrrolidine, ethyldimethylamine, dimethylethanolamine, 3-methoxypropylamine, diethanolamine, dimethylisopropanolamine, methyldiethanolamine, morpholine, piperidine, cyclohexylamine, diethylethanolamine, di-n-propylamine, diisopropylamine, n-methylmorpholine, n-eththylmorpholine, di-n-butylamine diisobutylamine, triethylamine, and dimethylaminopropylamine. In some embodiments, additive regulator 190 may include a neutralizing amine pump and a filming amine pump. In some embodiments, the controller 150 may be manually overridden or automatically overridden by high priority instructions. The amount, type, and/or location of the additive injected into the process stream may be selected based on information from one or more of the sensor arrays 135, 140a-c., such as pH, chloride level, ammonia, total nitrogen, and estimated water dew point pH.
In support of the teachings herein, various analysis components may be used in the controller 150 and/or monitor 160, including digital and/or analog systems. The controller 150 and/or monitor 160 may have components such as a processor, storage media, memory, input, output, communications link (wired, wireless, pulsed mud, optical or other), user interfaces, software programs, signal processors (digital or analog) and other such components (such as resistors, capacitors, inductors and others) to provide for operation and analyses of the apparatus and methods disclosed herein in any of several manners well-appreciated in the art. It is considered that these teachings may be, but need not be, implemented in conjunction with a set of computer executable instructions stored on a computer readable medium, including memory (ROMs, RAMs), optical (CD-ROMs), or magnetic (disks, hard drives), or any other type that when executed causes a computer to implement the method of the present disclosure. These instructions may provide for equipment operation, control, data collection and analysis and other functions deemed relevant by a system designer, owner, user or other such personnel, in addition to the functions described in this disclosure.
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One skilled in the art will recognize that the various components or technologies may provide certain necessary or beneficial functionality or features. Accordingly, these functions and features as may be needed in support of the appended claims and variations thereof, are recognized as being inherently included as a part of the teachings herein and a part of the disclosure disclosed. The probes and methods herein may be non-explosive and/or explosive-proof. The methods and apparatuses may also be advantageously employed at relatively high temperatures, for instance up to 200° C., or even higher.
While the disclosure has been described with reference to exemplary embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the disclosure. In addition, many modifications will be appreciated by those skilled in the art to adapt a particular instrument, situation or material to the teachings of the disclosure without departing from the essential scope thereof. Therefore, it is intended that the disclosure not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this disclosure, but that the disclosure will include all embodiments falling within the scope of the appended claims.
The words “comprising” and “comprises” as used throughout the claims is to be interpreted to mean “including but not limited to”.
This application claims priority from U.S. Provisional Patent Application Ser. No. 61/377,122, filed on 26 Aug. 2010, the disclosure of which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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61377122 | Aug 2010 | US |