The invention relates to compression refrigerator control systems, viz. to refrigerant composition control in premixed refrigerant cycle of liquefied natural gas production.
WO 2012125018 discloses a method for controlling the natural gas liquefaction process in a mixed refrigerant unit, which method comprises periodical monitoring of the current process parameters and controlling the refrigerant composition in a main cryogenic heat exchanger (MCHE) for achieving the optimum process parameters. This method primarily uses an «instruction control system» as a program code providing maintenance of the desirable MCHE temperature profile.
The disadvantages of the known method are insufficient control accuracy and speed in the rapidly changing ambient temperature conditions. Furthermore, the known method provides natural gas liquefaction using a single mixed refrigerant circuit.
The natural gas liquefaction technology with a double mixed refrigerant (DMR), as disclosed, for example, in the monograph of E. B. Fedorova «State-of-the-art and development of the global liquefied natural gas industry: technologies and equipment», Moscow: I. M. Gubkin Russian Oil and Gas University, 2011, p. 80-82, uses two streams of circulating mixed refrigerant: in the pre-cooling circuit and in the liquefying circuit.
The purified natural gas and mixed refrigerant (MR) of the main liquefaction cycle are cooled in the pre-cooling cycle to the temperature between −50 and −80′ C. serially passing up the HE1 and HE2 tube nests.
MR consisting primarily of methane and ethane with some content of propane and nitrogen is cooled in HE1 and partially condensed in HE2, then split in a separator S1 into two streams (liquid and gas) passing up to the HE3 tube nests. The main liquefaction cycle refrigerant is removed from HE3 bottom, and fed for suction to a two-stage compressor C1,2, where it is compressed, cooled, and returned to HE1.
In MCHE (HE3), the natural gas is passed up the tube nests, liquefied, and supercooled to −153° C. After the MCHE, the compressed and liquefied gas is expanded in T1 to 0.12-0.13 MPa, cooled to −101° C., and fed to a storage vessel.
The pre-cooled mixed refrigerant (PMR) is a mixture of ethane and propane with a slight content of methane. Use of mixed refrigerant in the pre-cooling cycle makes the process more flexible and effective in the low temperature conditions of ambient air. The process can be readily adapted to the changing ambient temperature by varying the PMR component ratio.
However, the refrigerant composition control for minimizing the PMR cycle temperature with respect to the current ambient temperature is extremely difficult due to a limited vapor make-up rate. For such great volume of PMR cycle, limited vapour make-ups leads in limited rate of changing PMR composition. Due to the optimum PMR composition changing along with the ambient temperature and limited rate of changing PMR composition even at the daily temperature fluctuations, the composition will be often far from optimum.
The technical problem, which is be solved by the invention, is to develop a method for controlling the pre-cooled mixed refrigerant composition, which method allows optimizing the PMR composition via accurate and stable control. The technical result is higher efficiency of the pre-cooling cycle due to maintaining the optimum PMR composition and thus minimizing the cooled product temperature in LNG production
The given problem is solved and the technical result is achieved by the method for controlling the refrigerant composition in the PMR cycle of LNG production, wherein control is carried out in view of the weather forecast temperature, and the method comprises the steps of measuring the concentration of each PMR component; measuring the ambient temperature; calculating the required concentration of each component for each of the measured and weather forecast temperatures on the basis of the predetermined relationship between the optimum concentration of each component and ambient temperature; calculating the time period required to change appropriately each component concentration in transition to the following of the weather forecast temperatures by using the highest possible change (increase or decrease) rate of each component concentration for the said cycle; and comparing the measured and required concentration of each component in view of the calculated time periods and direction of change in the component concentrations during these periods.
The increasing concentration of each component is measured by make-up this component into the cycle, and the decreasing concentration thereof is measured by make-up other components into the cycle.
The PMR components are methane, ethane, and propane.
The daily weather forecast is preferably obtained along with the temperature data every hour.
Preferably, the time periods, which are selected from the periods, exceed the time period between two adjacent temperature values from the weather forecast, and the measured and required concentrations of each component are compared in view of the selected time periods.
The invention is explained with figures.
The major objective of controlling the PMR composition is minimizing the cycle temperature in view of the current ambient temperature. Thus, minimized temperature is the temperature of natural gas (NG) leaving the PMR cycle. Further, it indicates the work saved in the MR cycle of NG liquefaction that allows for the same maximum load of MR compressor to produce more product (i.e. to liquefy more NG).
It should be understood that the lighter is the PMR composition, the more effective is the PMR cycle since heat exchangers HE1 and HE2 (
Therefore, the optimum temperature of PMR components depends upon the ambient temperature. This dependence for each of the PMR components may be obtained experimentally for the particular LNG production unit.
It is essential to note that a preferable PMR cycle comprises make-up the components, i.e. to decrease the concentration of any PMR component, two others should be added. The PMR components may be added by opening the make-ups. Ethane and propane may use both gas and liquid make-ups, while methane may be added only as a gas. In the make-up process, excess liquid creating excessive level in the separator (provisionally not shown) at C3 outlet is drained (to a fractionating unit) that further promotes to lower concentration of the component, while other components existing in the gas phase in the same separator (primarily, methane) create excessive pressure and removed to MR cycle.
The ambient temperature may significantly vary, especially in autumn and spring, when the temperature drop may be up to 15° C. in a short period of time. For this reason, controlling the PMR composition only in view of the current ambient temperature with respect to the limited PMR composition change rate leads in a non-optimum PMR composition.
To achieve or at least approach to the optimum concentrations of PMR components, controlling the PMR composition according to the invention is carried out in view of the weather forecast temperatures.
The weather forecast is preferably provided as the hour temperature data in advance for 24 hours, e.g. from 5 a.m. to 5 a.m. of the next day. The weather forecast may be updated each 12 hours.
The concentration of each PMR component and ambient temperatures are measured to calculate the required concentration of each component for each of the measured and weather forecast temperatures on the basis of the predetermined relationship between the optimum concentration of each component and ambient temperature.
Then for each of the weather forecast temperatures the required time period is calculated to change (increase or decrease) appropriately each component concentration in transition to the following weather forecast temperature, in particular, to the next hour temperature, by using the PMR cycle with the maximum possible change (increase or decrease) rate of each component. The said rates may be calculated or determined experimentally.
The time periods, which are selected from the calculated periods, exceed the period between two adjacent weather forecast temperature values, in particular, the periods exceeding 1 hour (for the hourly weather forecast).
Then the measured concentration of each component is compared to the required one and each component concentration is varied in view of the selected time periods and the direction of changing the component concentrations during these periods.
For this purpose, it is necessary to calculate the excess of the selected tune periods over the time period 1 hour) between two adjacent weather forecast temperatures, and the relevant component concentration measuring is started in advance with respect to the said excess as welt as to the direction of the component concentration change, where the comparison with the required concentration is carried by using either the lower or upper permissible limit thereof.
As shown in
Number | Date | Country | Kind |
---|---|---|---|
2018125814 | Jul 2018 | RU | national |