HCBBS Forum (English)
Submit Chemical Projects / Find Solutions
Amplify Your Requirements on a Broader Chemical Platform *Engineering · Technology · Equipment · Solutions*
Submit Request

Control measures for coking in the fractionation system of heavy oil catalytic cracking units

2008-01-15View Original

Thread Content

Control Measures for Coking in the Fractionation System of Heavy Oil Catalytic Cracking Units Abstract: This paper discusses the mechanisms and basic characteristics of scaling and coking in the fractionation system of heavy oil catalytic cracking units, analyzes the control factors associated with scaling and coking in different areas, conducts a quantitative analysis of these control factors, identifies the quantitative relationships between them, and proposes specific control measures to address scaling and coking, thereby providing guidance for practical operations. Keywords: catalytic cracking unit; fractionation tower; slurry; sediment formation; operating conditions; optimization. 1 Characteristics of scaling and coking in different parts of the fractionation system. 1.1 Bottom of the fractionation tower: Since the operation of the heavy oil catalytic cracking unit (RFCCU) began, coking at the bottom of the fractionation tower has not affected safe production; however, the thickness of the scale there exceeds 800 mm, which has blocked the bottom filter. The nozzles in the stirring steam distribution ring at the bottom of the tower as well as those in the slurry return distribution ring are also blocked. As the slurry flows through the distillation system, and as the scale deposits grow, under the influence of gravity and viscosity, these deposits fall into the areas of slow liquid flow and settle on the walls of the vessels. The diameter of this distillation column is 3.8 m, and a stable liquid level is maintained at the bottom of the column; as a result, the oil slurry spends the longest time there. Furthermore, the linear velocity of the slurry flowing at the bottom of the tower is not uniform; there are slow-flow areas and dead zones at the bottom of the tower, as well as a stagnant boundary layer on the tower walls. These conditions create the necessary environment for the gravitational deposition of scale deposits. As a result of heat transfer and washing between the circulating slurry in the de-overshooting section and the reaction gas slurry (containing coke fragments from large oil and gas pipelines), the bottom slurry of the tower has the highest liquid phase temperature and the highest scale nucleation concentration among all sections of the tower. With the high temperature of the oil slurry at the bottom of the tower, the thermal polymerization reactions of the coking-prone substances on the scale deposits intensify. Additionally, when the level of the circulating oil slurry is high at the bottom of the tower, the residence time increases, which leads to more thermal condensation reactions. All of these lead to coking on the tube walls of the tower. The scaling and coking at the bottom of a distillation tower have the following characteristics: ① The structure of the scale layer at the bottom of the tower can be divided into three layers: the upper layer is a pile of scale particles, which is very soft and easy to remove; the middle layer is a transitional layer that is soft and elastic with high viscosity; the lower layer is a coked layer that is hard and tough, making it extremely difficult to remove. ②Depending on the length of the production cycle, the temperature at the bottom of the tower, and the composition of the slurry, there are significant differences in the thickness and structure of the fouling layer at the bottom of the tower. When scaling and coking at the bottom of the tower are severe, a scale layer also forms on the tower walls. The height of the scale layer at the bottom of the tower exceeds that of the filter, resulting in a decrease in the oil slurry circulation rate. If the content of broken coke in the slurry is high, some very fine fragments of coke can also enter the slurry circulation system and clog the heat exchanger tubes. ③The bottom of the tower is the zone with significant thermal reactions. If the temperature of the liquid phase at the bottom of the tower is controlled too high, on the one hand, substances prone to coking and scale nuclei will concentrate; on the other hand, the thermal polymerization reaction of these coking-prone substances on the scale deposits in the oil slurry at the bottom of the tower will intensify, increasing its viscosity. This promotes scaling at the bottom of the tower, as well as in the oil slurry heat exchangers and oil slurry steam generators. ④The degree of scaling is controlled by the content of scale particles in the slurry and its viscosity.   1.2 Slurry circulation pipeline: During various maintenance operations on the RFCCU, scaling in the slurry circulation pipeline of the distillation system has been observed to some extent in every case. As the slurry flows through the circulation pipes, a laminar boundary layer exists at the bottom of the pipes. The deposits located at the very bottom of this laminar boundary layer settle at the pipe bottom due to gravity. Since the temperature at the pipe bottom is **lower than that of the flowing fluid, the viscosity of these deposits increases there, leading to scaling. The scaling in the slurry circulation pipes has the following characteristics: ① The degree of scaling is determined by the degree of coking of the scale-forming substances at the bottom of the distillation tower; the resulting scale layer is wavy in shape and soft in texture, making it easy to remove. Its coking macroscopic phenomenon is not obvious. ②When scaling is severe, it causes poor flow rate in the slurry pump, a decrease in outlet pressure, and a reduction in the slurry circulation volume.   1.3 Slurry Heat Exchanger (Steam Generator) The RFCCU slurry steam generator often gets clogged. During the emergency repair in April 1997, it was found that the thickness of the scale buildup in the tube boxes reached 500 mm, and one-third of the tube bundles were blocked. The steam generation capacity of the slurry steam generator has declined significantly. Heat exchanger scaling has the following characteristics: ① The scaling process in the tube sheet and small floating heads occurs through gravitational deposition, and the degree of scaling is determined by the content of scale nuclei in the slurry as well as the flow rate. The scaling process in the tube bundle occurs through cooling-induced viscous deposition, and the degree of scaling is controlled by the presence of scale nuclei in the slurry, the amount of substances prone to coking, and the flow rate. ②The scaling on the tube sheet and small floating heads accelerates each other in conjunction with the scaling on the tube bundle: the scaling on the tube bundle reduces the flow velocity of fluid at the inlet of the tube sheet and small floating heads, increasing the degree of fluid stagnation there and thus leading to more severe scaling on those components. At the same time, as the scale layer thickens, on the one hand, the inlet to the tube bundle near the scale layer is gradually blocked by it, and on the other hand, this increases the transport of scale particles toward that tube bundle, until the tube bundle becomes blocked. ③The scale in the tube bundles contains a significant amount of substances prone to coking. Although the scale is soft in texture, it is highly sticky and difficult to remove completely. The macroscopic phenomenon of coking in the fouling on the tube sheet and small floating heads is not obvious; the fouling is soft in texture and contains a high amount of organic matter.   1.4 De-overshooting Section: Previous shutdown inspections conducted by the RFCCU revealed that hard, compact carbon deposits ranging in thickness from 5 to 20 mm had formed on the chevron baffles and the tower walls in the de-overshooting section of the fractionation tower. When the gas-phase load increases significantly, the amount of slurry returning to the tower does not increase in a timely manner. This leads to a low liquid-phase spray density in the desuperheating section, as well as an unreasonable distribution of the gas-liquid phase loads, resulting in localized overheating. The reactivity of substances prone to coking and scale formations increases in these overheated areas, thereby triggering coking reactions. Scale deposits form at the cooling zones located on the chevron baffles or tower walls; these deposits have strong adhesive properties, allowing them to attach other substances prone to coking and scale formations, thus creating further scale layers. Due to the very high temperature of the liquid phase in the desuperheating section, which averages 320–370°C, once scaling occurs, the scale layer will undergo deep carbonization from the inside out, forming a char layer. Coking characteristics in the desuperheating section: ① The substances prone to form coke and scale exhibit rapid reaction properties. ②The scaling mechanism in the desuperheating section is the deposition of scale particles through excessive aggregation and viscosity increase. The excessive condensation of coking-prone substances and scale aggregates causes the product to tend to form deposits on the walls; the degree of coking is determined by the temperature of local hot spots as well as the viscosity of these coking-prone substances and scale aggregates. ③In an environment free from superheating, the scale layer transforms into a char layer, upon which a thin layer of scale adheres, being quite hard in texture.   1.5 First and second stage trays and their tongue holes: From June to August 1999, dozens of column flooding incidents occurred repeatedly in the RFCCU distillation column. The frequency of such incidents increased from 1–2 times every two weeks at first to 3–4 times per week later on; the duration of each incident rose from 1–2 hours initially to 5–8 hours thereafter. This made it impossible to control the distillation process, resulting in frequently substandard product quality and posing a serious threat to the safe operation of the facility. During the shutdown for inspection of the fractionation tower, it was found that, first, the first and second layers of the tongue-shaped trays were covered with a scale layer about 60–70 mm thick; the tongue holes in the first layer of trays were partially or completely blocked by this hard scale layer, with 90% of the holes being completely blocked, and in those that were partially blocked only the tip of the tongue portion remained unobstructed. The reason for the blockage of the orifice holes is that the oil and gas coming from the superheating removal section are not thoroughly washed; these oils and gases carry with them substances prone to coking, scale nuclei, and scale deposits from the oil slurry. These substances accumulate and settle due to gravity. Scaling occurs in the orifice hole area because it is a region with slow flow – under the influence of inertial forces and viscous forces, the substances prone to coking and scale deposits come into contact with the base of the orifice hole, forming scale deposits. In particular, high-viscosity macromolecular gums, asphaltenes, and their associated scale deposits further condense and carbonize in the high-temperature oil and gas environment, forming stable scale deposits that gradually accumulate over time. Fouling characteristics of the tray and its waffle holes: ① The tray suffers from gravity deposition fouling, while the waffle holes experience viscous deposition fouling. ②The degree of fouling in the tongue hole is controlled by the number of high-viscosity fouling masses in the oil and gas after washing, as well as by temperature.   2 Control Measures 2.1 Control factors for scaling and coking in the bottom of the tower and the slurry circulation system. Scaling in the slurry circulation pipes at the bottom of the tower and in the tube banks of the slurry heat exchangers is the result of the gravitational deposition of scale particles; the growth of these scale layers is controlled by the size and viscosity of those particles. Scaling in the tube bundles of the slurry heat exchangers is caused by the viscous deposition of scale particles and asphaltenes, and the growth of such scale layers depends on the viscosity, concentration, and flow rate of these particles and asphaltenes. Therefore, it is crucial to control the growth of these scale particles and the increase in their viscosity. The linear velocity of the tube bundle in the slurry heat exchanger is another key control factor for tube bundle scaling. The degree of growth of the scale mass can be expressed by the magnitude of the increase in the average particle size of the scale mass, Δd; the factors that influence Δd are shown in Figure 1.   As the increase in viscosity of the sludge mass, Δη increases, and Δd also increases. The control factors for Δη are shown in Figure 2.   2.1.1 Content of coking-prone substances, scale nuclei, and scale aggregates (L1) L1 is the average value of the content of coking-prone substances (scale nuclei or scale aggregates) in the bottom oil slurry at time t0, expressed in kg/m3; L1′ is the average value of such content at time t0 + Δt, also expressed in kg/m3. Assuming the slurry system is homogeneous, the effect of the coking reaction at the bottom of the tower on the content of coking-prone substances (scale nuclei or scale aggregates) can be ignored. Its functional relationship is: L′1 = L1 + l1FΔtV1 – L1YΔtV1ρ (1) Where: l1 —— the content of coking-prone substances (scale nuclei or scale aggregates) in the reactant oil and gas, expressed in kg/t; Y —— the output volume of the oil slurry, in kg/h; F —— the total processing volume, in t/h; V1 —— the volume of the entire oil slurry circulation system, in m3; ρ —— the density of the oil slurry, in kg/m3.    For Set II RFC CU, V1 can be expressed as: V1 = 27.20X/100 + 6.47 – 0.06 + 17.22 = 0.272X + 23.63. In equation (2), X represents the actual liquid level at the bottom of the distillation tower, in %.   l1 is related to the coking tendency of the feed oil, the degree of cracking, the coking content in large oil and gas pipelines, the metal oxide content, and the efficiency of the cyclone separator. The controls for L1 are as follows: ① To keep L1 in balance, when F or l1 or ρ increases, Y must also increase accordingly. It can be seen from this that Y is a control variable for L1. ②To prevent L1 from exceeding the limits, it is necessary to carry out proper monitoring, analysis, and control of L1. ③When an increase in F or l1 or ρ is detected, the amount of slurry discharged should be increased appropriately at the right time. The following requirements apply to the control of l1: ① Strengthen the monitoring of the properties of the crude oil and slurry, in order to analyze the changes in l1. ②Depending on the different raw materials and production methods, an appropriate degree of cracking is controlled to prevent l1 from becoming too high. ③During major overhauls, it is necessary to intensify the coking removal and maintenance work on cyclone separators and large oil and gas pipelines.   2.1.2 Average residence time (τ1) of the slurry system: The residence time of the slurry in the distillation system refers to the time it takes for the slurry to enter the distillation tower and exit it, and can be expressed by the average residence time τ1 of the slurry system. For the fractionation system of Set II RFCCU: τ1 = V1ρ/Y = (0.204X + 17.72)/Y (h) (3). At temperatures between 300 and 350°C, ρ = 750 kg/m3; therefore, to control τ1, it is necessary to: ① Keep τ1 low when L1 is large, in order to maintain equilibrium in Δd. In fact, as can be seen from equations (1) and (3), increasing Y will reduce both τ1 and L1; thus, it is evident that Y is the control variable for Δd. ②For Set II RFCCU, τ1 is generally controlled at 4–6 hours. 2.1.3 Average residence time of the bottom slurry (τ2) The residence time of the bottom slurry refers to the time it takes for the slurry to enter the bottom of the tower and then leave it; this can be denoted by τ2. τ2 can be calculated by taking the ratio of the mass of the bottom slurry to the mass flow rate of the slurry in circulation.   τ2=60V2ρ/Q=(11.9X+281)/Q (minutes) (4) Where the volume of the oil slurry at the bottom of the tower is: V2=27.20X/100+6.47-0.06=0.272X+6.41 (m3) (5) At 350°C, ρ=730 kg/m3; where Q represents the total circulation rate of the oil slurry, in kg/h. Therefore, the control of τ2 involves: ① To maintain the balance of Δη, the value of τ2 is constrained by L1, T, and Δd. ②Q serves as a means to regulate both T and the temperature of the first tray, but it is also constrained by the design values of the slurry pump; therefore, the value of τ2 remains relatively stable, and it is generally not used as a means for regulating w. ③For Set II RFCCU, τ2 is generally kept between 5 and 6 minutes.   2.1.4 Temperature (T) of the slurry at the bottom of the distillation tower: The bottom temperature refers to the average temperature of the slurry at the bottom of the distillation tower. By the time the slurry exits the outlet at the bottom of the tower, it has been well mixed, and the temperature here can represent the average temperature of the slurry at the bottom of the tower. The controls for T include: ① In the control function for Δη, production experience shows that T and Δd are effective means for maintaining equilibrium in Δη, with Δη being more sensitive to T. ②At 350°C, Δη experiences a sudden change; when T exceeds 350°C, coking intensifies. ③Set II of the RFCCU keeps T below 345°C over the long term.   2.1.5 Flow velocity (S) in the tube bundle of the slurry steam generator: In heat exchangers and pipes, if the flow velocity is too low, scale deposits can easily form due to gravity, leading to blockages in the slurry system. A recommended line speed is generally 1.5 to 2.4 m/s.   S = Q′/3600ρA3 = Q′/185 (m/s) (6) Where: A3 —— the cross-sectional area of the tube bundle in the first quadrant of the slurry steam generator’s tube box, taken as 0.0675 m2; Q′ —— the flow rate of the slurry passing through the slurry steam generator, in kg/h.    At 310°C, ρ = 760 kg/m3.    The controls for S include: ① The S value of the two sets of RFCCU is below the recommended value; only by reducing the value of Δη and keeping R at a slightly lower level can scaling and coking be effectively controlled. ②When there is a surplus of heat available, the S value can be increased by blocking some of the tubes in the oil slurry steam generator’s tube bundle.   2.1.6 Other control factors ① The use of scale inhibitors can prevent the caking of scale deposits. ②Renovation of the slow-flow zone. To improve flow in the slow-flow zone, some plants have installed steam agitators at the bottom of the distillation tower, achieving certain results. To prevent the sieve pores of the filter at the bottom of the tower from becoming clogged, it is possible to increase the diameter of these sieve pores and thus expand their flow area. This approach not only enhances flow in the slow-flow zone but also extends the service life of the filter at the bottom of the tower.   2.2 Control factors for scaling and coking in the superheating removal section and the first and second tray levels The key control points for scaling and coking in the superheating removal section and the throat openings of the first and second trays are the formation and growth of scale deposits. The degree of coking in the desuperheating section is denoted by W1, and the factors affecting its formation are shown in Figure 3.   The coking degree of the trough openings on the first and second tray levels is denoted by W2; the factors affecting its formation are shown in Figure 4. The degree of fouling on the first and second tray levels is denoted by W3; the factors affecting its formation are shown in Figure 5.   2.2.1 Slurry Recirculation Rate (Q1) UOP recommends a minimum slurry recirculation rate of 120% of the total feed volume, or 37 m3/h per meter of tower diameter. The control of Q1 includes: ① As can be seen from the control diagrams of W1 and W2, in order to maintain the balance of W1 or W2, the value of Q1 is determined by L1 and l1. L1 and l1 cannot be used as control variables for W1 and W2; the control variable is Q1. ②The reflux oil slurry can remove the excess heat from the reaction gases, thereby controlling the temperature of the first tray in the tower; it also helps to control the degree of scaling and coking in the desuperheating section of the distillation tower as well as in the trays above it. ③Based on the actual operating conditions of the second set of RFCCU, the lower limit value for the amount of slurry returning to the reactor is given as FN: FN = max (7). In this formula, F1 represents the volume of fresh feed, in t/h; F2 represents the volume of reprocessed oil flowing back, in t/h; F3 represents the volume of modified gasoline flowing out, in t/h; F4 represents the volume of terminator used, in t/h; F5 represents the volume of water or another substance used as a terminator, in t/h. 2.2.2 Saturation degree and the amount of reprocessed oil returning to the tower (Q2): The amount of internal reflux below the extraction tray in the reprocessed oil stream is determined by the saturation degree of the reaction gas after overheating is removed. Too low a reflux flow rate in the first and second tray levels, along with too low a supersaturation level or even a dry tray condition, will accelerate coking in the first and second tray levels as well as their wick holes. Excessive supersaturation results in the heat contained in the reaction gas and oil not being effectively recovered at the bottom of the tower, which is detrimental to energy conservation in the facility. Therefore, controlling the appropriate supersaturation of the de-superheated reaction gas oil is important for the long-term operation of the fractionation tower and energy savings.   3 Conclusion In continuous production, it is very difficult, if not impossible, to completely eliminate scaling and coking in all parts of the distillation system. However, as long as people understand the patterns of scaling and coking in distillation systems, it is still possible to effectively control these phenomena, reduce their negative impact on normal operations, and ensure the safe and prolonged operation of the facilities.

Submit a Project

**Looking for Chemical Technology, Equipment & Solutions?** No Registration Required Broader Platform Exposure | Global Chemical Service Provider Connections

Submit Request — Free Consultation

Disclaimer

This is an automated machine translation of the original thread. Some technical terms may have inaccuracies; the original text shall prevail. Click "View Original" at the top right to access the source page, which supports IP-based automatic real-time language translation. Please watch out for contact details and sales inducements to prevent fraud. All content and translations are for reference only, representing solely the poster's personal views. For enquiries, email service@hcbbs.com.