Patent Grant
7421856
This invention relates generally to cryogenic air separation and, more particularly, to cryogenic air separation employing a double column.
Cryogenic air separation systems which employ downflow main condensers typically employ recirculation pumps to ensure adequate wettability of boiling passages during normal as well as part-load operation. Liquid recirculation from the column sump through the boiling passages results in good heat transfer performance as well as enabling satisfaction of the safety criteria of preventing oxygen boiling to dryness. However, recirculation pumps increase cost, reduce reliability and reduce efficiency of the system due to the power penalty incurred to run the pump.
A method for operating a cryogenic air separation plant having a higher pressure column and a lower pressure column comprising passing nitrogen vapor from the higher pressure column to the upper portion of a once-through main condenser, flowing oxygen liquid from the separation section of the lower pressure column to the upper portion of the once-through main condenser, passing the nitrogen vapor and the oxygen liquid down the once-through main condenser in heat exchange relation wherein at least some but not all of the downflowing oxygen liquid is vaporized, and withdrawing both oxygen vapor and oxygen liquid from the once-through main condenser in a liquid to vapor mass flowrate ratio within the range of from 0.05 to 0.5.
As used herein, the term “separation section” means a section of a column containing trays and/or packing and situated above the main condenser.
As used herein, the term “enhanced boiling surface” means a special surface geometry that provides higher heat-transfer per unit surface area than does a plain surface.
As used herein, the term “high flux boiling surface” means an enhanced boiling surface characterized by a thin metallic film possessing high porosity and large interstitial surface area which is metallurgically bonded to a metal substrate by means such as sintering of a metallic powder coating.
As used herein, the term “column” means a distillation or fractionation column or zone, i.e. a contacting column or zone, wherein liquid and vapor phases are countercurrently contacted to effect separation of a fluid mixture, as for example, by contacting of the vapor and liquid phases on a series of vertically spaced trays or plates mounted within the column and/or on packing elements such as structured or random packing. For a further discussion of distillation columns, see the Chemical Engineer's Handbook, fifth edition, edited by R. H. Perry and C. H. Chilton, McGraw-Hill Book Company, New York, Section 13, The Continuous Distillation Process. The term, double column is used to mean a higher pressure column having its upper end in heat exchange relation with the lower end of a lower pressure column. A further discussion of double columns appears in Ruheman “The Separation of Gases”, Oxford University Press, 1949, Chapter VII, Commercial Air Separation.
Vapor and liquid contacting separation processes depend on the difference in vapor pressures for the components. The high vapor pressure (or more volatile or low boiling) component will tend to concentrate in the vapor phase whereas the low vapor pressure (or less volatile or high boiling) component will tend to concentrate in the liquid phase. Partial condensation is the separation process whereby cooling of a vapor mixture can be used to concentrate the volatile component(s) in the vapor phase and thereby the less volatile component(s) in the liquid phase. Rectification, or continuous distillation, is the separation process that combines successive partial vaporizations and condensations as obtained by a countercurrent treatment of the vapor and liquid phases. The countercurrent contacting of the vapor and liquid phases is generally adiabatic and can include integral (stagewise) or differential (continuous) contact between the phases. Separation process arrangements that utilize the principles of rectification to separate mixtures are often interchangeably termed rectification columns, distillation columns, or fractionation columns. Cryogenic rectification is a rectification process carried out at least in part at temperatures at or below 150 degrees Kelvin (K).
The sole FIGURE is a simplified representational schematic diagram of one preferred embodiment of the cryogenic air separation operating method of this invention.
In the practice of cryogenic air separation with downflow main condensers, it is necessary that the oxygen liquid flowing down the condenser not be completely vaporized so as to avoid the inefficient and dangerous boiling to dryness condition. To achieve this wetting, a liquid to vapor mass flowrate ratio (L/V) of greater than 0.5 and preferably from 1 to 4 is necessary for the fluid leaving the vaporizing passages of the condenser, and this criteria generally requires the recirculation of some liquid from the sump of the column to the boiling passages of the downflow main condenser.
The invention enables the operation of a downflow main condenser in a cryogenic air separation plant with an L/V within the range of from 0.05 to 0.5. During normal operation the reduced L/V requirement eliminates the need to recirculate liquid from the column sump to the vaporizing passages of the downflow main condenser. The once-through main condenser of this invention processes oxygen liquid from only the separation section of the column and employs boiling passages having an enhanced boiling surface, preferably a high flux boiling surface.
The invention will be described more fully with reference to the Drawing. Referring now to the FIGURE there is shown a partial schematic of a double column cryogenic air separation plant, having a higher pressure column 30 and a lower pressure column 31, and showing the placement of once-through main condensers 32, also referred to as condenser/reboilers, inside the lower pressure column. The main condenser/reboilers thermally link the higher pressure and lower pressure columns. Nitrogen vapor, at a pressure generally within the range of from 45 to 300 pounds per square inch absolute (psia), is passed in line 10 from higher pressure column 30 to the upper portion of the once-through main condenser or condensers wherein the nitrogen vapor exchanges heat with oxygen liquid as both fluids flow down through the once-through main condenser(s). The oxygen liquid, which is at a pressure generally within the range of from 1 to 100 pounds per square inch gauge (psig) is partially vaporized and the resulting oxygen vapor and remaining oxygen liquid are withdrawn from the once-through main condensers(s) as shown by flow arrows 34 and 33 respectively. The nitrogen vapor is completely condensed by the downflow passage through the once-through main condenser and the resulting nitrogen liquid is withdrawn from the once-through main condenser in line 11 and passed in lines 35 and 36 respectively as reflux into the higher pressure and lower pressure columns.
In the lower pressure column 31, oxygen liquid descending the column through packing 12 or trays (not shown) is collected in collector/distributor 13. Open risers 14 extend up from the floor of the collector box for the oxygen vapor generated in the main condenser to flow up through the column. Oxygen liquid from the collector flows through distributor pipe 15 and collects in the distributor section 16 of the individual modules. The oxygen liquid from the flow distributor section flows through the individual tubes or heat transfer passages where it is partially vaporized. These passages have enhanced boiling surfaces which significantly increases the ability of the liquid to wet the surface of the boiling side and reduces the amount of liquid flow needed to achieve wetting. The unvaporized liquid 17 collects at the bottom of the column and is withdrawn from the column as a product. The product boiler pump 18 is used to raise the pressure of oxygen to the required product pressure. The ratio of liquid to vapor mass flowrate (L/V) at the exit of the main condenser tubes or vaporizing passages ranges from 0.05 to 0.5, and is preferably within the range of from 0.2 to 0.4.
It is essential to maintain a minimum liquid flow rate over the boiling surfaces to ensure adequate wetting for the following reasons:
For the reasons given above, the specified liquid flow rate must be sufficient to provide a stable liquid film on the boiling surface. It should also be sufficient to ensure adequate wetting, i.e. that liquid is spread evenly across the boiling surface in each individual channel. Whether or not the liquid flow is sufficient to keep the boiling surfaces adequately wetted is a key design consideration. The flow rate for adequate wetting (defined as mass flow per unit width of the heat transfer surface in the flow direction) depends on:
The flowrate per unit width (ΓL) is:
ΓL=ML/W
Equations for predicting the minimum liquid flow required for wetting of a surface are expressed in terms of a liquid film Reynolds number, which is related to ΓL as follows:
The relationship between the liquid to vapor mass flowrate ratio L/V, the Reynolds number ReL and flow width (or perimeter) of the heat transfer surface W is given by:
Since adequate wetting of the boiling surfaces is important from safety considerations, a minimum liquid flow must be maintained. Thus, a criteria can be set either in terms of a minimum film Reynolds number (ReL) or minimum exit L/V (liquid to vapor mass flowrate ratio) to operate the main condenser/reboiler safely.
Experimental work has shown that with the practice of the invention one can operate at a lower L/V because of the following: unexpectedly better heat transfer performance requiring less surface area, reduction in wetted perimeter due to lower surface area and longer tube length, and unexpectedly better wettability characteristics of enhanced boiling surfaces.
In summary, the FIGURE shows relevant portions of a system for the cryogenic distillation of air that has the following characteristics:
When the cryogenic air separation plant is operated at certain part loads and when the liquid flow down the boiling passages is not sufficient to satisfy the wetting criteria, the product oxygen pump 18 may be used to pump some oxygen liquid to the boiling surface while the remainder of withdrawn oxygen liquid is passed in line 38 for recovery.
Although the invention has been described in detail with reference to certain preferred embodiments those skilled in the art will recognize that there are other embodiments of the invention within the spirit and the scope of the claims.
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| Number | Date | Country | |
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| 20060283208 A1 | Dec 2006 | US |
