GB1593539A - Pressure swing adsorption process for gas separation - Google Patents

Pressure swing adsorption process for gas separation Download PDF

Info

Publication number
GB1593539A
GB1593539A GB235880A GB235880A GB1593539A GB 1593539 A GB1593539 A GB 1593539A GB 235880 A GB235880 A GB 235880A GB 235880 A GB235880 A GB 235880A GB 1593539 A GB1593539 A GB 1593539A
Authority
GB
United Kingdom
Prior art keywords
bed
gas
adsorption
adsorption bed
flow
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB235880A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Greene and Kellogg Inc
Original Assignee
Greene and Kellogg Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Greene and Kellogg Inc filed Critical Greene and Kellogg Inc
Publication of GB1593539A publication Critical patent/GB1593539A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047Pressure swing adsorption
    • B01D53/0473Rapid pressure swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/10Inorganic adsorbents
    • B01D2253/104Alumina
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/10Inorganic adsorbents
    • B01D2253/106Silica or silicates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/10Inorganic adsorbents
    • B01D2253/106Silica or silicates
    • B01D2253/108Zeolites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2256/00Main component in the product gas stream after treatment
    • B01D2256/12Oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/10Single element gases other than halogens
    • B01D2257/102Nitrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40007Controlling pressure or temperature swing adsorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40035Equalization
    • B01D2259/40037Equalization with two sub-steps
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40035Equalization
    • B01D2259/40041Equalization with more than three sub-steps
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40043Purging
    • B01D2259/4005Nature of purge gas
    • B01D2259/40052Recycled product or process gas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40058Number of sequence steps, including sub-steps, per cycle
    • B01D2259/40062Four
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40058Number of sequence steps, including sub-steps, per cycle
    • B01D2259/40069Eight
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/40011Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40077Direction of flow
    • B01D2259/40081Counter-current
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2259/00Type of treatment
    • B01D2259/40Further details for adsorption processes and devices
    • B01D2259/403Further details for adsorption processes and devices using three beds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Separation Of Gases By Adsorption (AREA)

Description

PATENT SPECIFICATION ( 11) 1 593 539
O ( 21) Application No 2358/80 ( 22) Filed 24 Nov 1977 e ( 62) Divided out of No 1593538 ( 19) ( 31) Convention Application No 745285 ó ( 32) Filed 26 Nov 1976 in O ( 33) United States of America (US) ( 44) Complete Specification published 15 July 1981 i 1 ( 51) INT CL 3 B Ol D 53/04 ( 52) Index at acceptance Bl L 102 AB ( 54) PRESSURE SWING ADSORPTION PROCESS FOR GAS SEPARATION ( 71) We, GREENE & KELLOGG, INC, a corporation organised and existing under the laws of the State of Delaware, United States of America, of 290 Lockside Drive, Tonawanda, New York 14150, United States of America, formerly of 1716 Main Street, Buffalo, New York 14209, United States of America, do hereby declare the invention for which we pray that a patent may be granted to us, and the 5 method by which it is to be performed, to be particularly described in and by the following statement:-
This invention relates to a process for separating gas mixtures by pressure swing adsorption.
One area of use of the present invention is in fractionating air to provide a 10 product stream of high purity oxygen, although the principles of the present invention can be applied in other fields.
In basic pressure swing adsorption processes and systems for separating air, adsorption is carried out at a high pressure and desorption is carried out at a low pressure Compressed air is introduced into a fixed bed of adsorbent material so 15 that the nitrogen thereof is then preferentially adsorbed to produce oxygen-rich product gas When the adsorption bed is about saturated, the bed pressure is reduced to desorb nitrogen from the adsorbent material and to regenerate the adsorption capacity A purge by some of the product or an intermediate process stream often is used in order to increase the efficiency of regeneration To facilitate 20 continuous operation, two or more adsorption beds are employed so that while one bed performs adsorption the other bed undergoes regeneration.
In the design and operation of pressure swing adsorption processes and systems, it would be highly desirable to provide maximum utilisation of adsorbent material in the adsorption beds, to reduce the energy requirements for operation 25 of the system, to obtain a substantially constant degree of product purity, and to reduce adsorbent material requirements while maintaining a high degree of product purity along with improved efficiency and reliability.
Accordingly, the present invention provides a pressure swing adsorption process using at least one adsorption bed having a gas inlet and a gas outlet and at 30 least one storage adsorption bed which is segregated from the gas inlet of said at least one adsorption bed and is able to be communicated with the gas outlet of said at least one adsorption bed, comprising the steps of flowing a feed gas mixture into said inlet of said at least one adsorption bed to adsorb at least one gas of said mixture within said bed while flowing the remainder of said gas mixture out of said 35 bed outlet as product gas until said adsorption bed is about saturated with said one gas and the purity of said product gas has reduced; flowing reduced purity product gas from said bed outlet into said segregated storage adsorption bed by depressurising said at least one adsorption bed into said segregated storage adsorption bed until the mass transfer zone within said adsorption bed moves into 40 said segregated storage adsorption bed, closing the flow path between said adsorption bed and said segregated storage adsorption bed; purging said one bed in a countercurrent direction; and flowing gas from said segregated storage adsorption bed back into said adsorption bed by depressurising said segregated storage adsorption bed and repressurising said purged at least one adsorption bed 45 In order that the present invention may more readily be understood, the following description is given, merely by way of example, with reference to the accompanying drawings, in which:Figure 1 is a schematic diagram of a pressure swing adsorption system for carrying out a process according to the present invention; Figure 2 is a cycle sequence chart illustrating the pressure swing adsorption 5 process of the present invention; Figure 3 is a schematic diagram of another embodiment of pressure swing adsorption system for carrying out a process according to the present invention with some parts removed; and Figure 4 is a schematic block diagram of a control arrangement for carrying 10 out a pressure swing adsorption process according to the present invention.
Referring now to Figure 1, there is shown a system for carrying out a pressure swing process according to the present invention, for fractionating at least one component from a gaseous mixture by adsorption The gaseous feed mixture is supplied to the system by a feed gas stream which flows along an input conduit 10 15 and is moved therealong by means of a pump or compressor 12 Although the present process is specifically described and illustrated in relation to the fractionation of air, by pressure swing adsorption, to produce an oxygenrich product gas stream, the present invention is broadly applicable to the separation of any organic and/or inorganic gas mixtures 20 The system includes a bed A, in a first adsorption bed vessel 16 having a gas inlet 18 and a gas outlet 20 The system further includes at least one additional adsorption bed B in a bed vessel 24 having a gas inlet 26 and a gas outlet 28.
A preferred vessel construction includes an outer pressure cell with an inner annulus 25 Many adsorbent materials are well-known in the art, and examples of typical adsorbent materials for use in adsorption beds include natural or synthetic zeolites, silica gel, alumina and the like Generally, the adsorbent beds in a system contain the same adsorbent material, however, each bed may contain a different type of adsorbent material or different mixtures of adsorbent material as desired 30 The system of the present invention further comprises a segregated storage adsorption bed C in a vessel 32, which does not communicate with the feed gas stream from conduit 10; in the system shown in Figure 1, gas is introduced to and withdrawn from bed C at the same end via a conduit 34 In the system shown, adsorption bed C is approximately the same size as the adsorption beds A and B 35 and may contain the same type of adsorbent material, but the segregated storage adsorption bed C can instead be smaller in size, may include different adsorbent material, and may be operated at a different capacity as compared to the adsorption beds A and B. The gas inlet 18 of adsorption bed A is connected to the feed gas stream 40 conduit 10 by suitable conduits including an automatic valve 40 A, and similarly the gas inlet 26 of adsorption bed B is connected to the feed gas stream conduit 10 by suitable conduits including an automatic valve 40 B. The system further includes a waste gas outlet 44 which can be open to the atmosphere or which can communicate with a waste gas stream The gas inlets 18 45 and 26 of adsorption beds A and B, respectively, also are connected to the waste gas outlet 44 by suitable corresponding conduits including automatic valves 46 A and 46 B, respectively The automatic valves 40 A and 40 B and 46 A and 46 B, and additional automatic valves to be described later, can of the solenoidoperated type, but in any event are of the type which can be operated to be either fully open 50 or fully closed.
Suitable conduits define a gas flow path connected at one end to gas outlet 20 of adsorption bed A and at the opposite end to gas outlet 28 of adsorption bed B A first flow control valve 50 A is positioned in the gas flow path between gas outlet 20 of adsorption bed A and adsorption bed B Valve 50 A allows unrestricted gas flow 55 therethrough in the direction from bed A toward adsorption bed B, and provides controlled flow therethrough in the reverse direction The controlled flow preferably is provided by manual adjustment A second flow control valve 50 B in the gas flow path between gas outlet 28 of adsorption bed B and the adsorption bed A allows unrestricted gas flow therethrough in the direction from bed B toward bed 60 A, and provides controlled flow, preferably manually controlled, therethrough in the reverse direction Valves 50 A, 50 B are preferably identical and can be of the type known commercially as Parker-Hannifin flow control valves An isolation valve, in the form of an automatic valve 54, is provided in the gas flow path between 1,593,539 gas outlets 20 and 28 of the adsorption beds A and B, preferably between gas outlet of adsorption bed A and the flow control valve 50 A.
A second gas flow path between beds A and B is provided by suitable conduits or piping which joins the gas outlets 20 and 28 of the beds In this second path a first automatic valve 60 A is connected adjacent outlet 20 of bed A, and a second 5 automatic valve 60 B is connected adjacent outlet 28 of adsorption bed B The segregated storage adsorption bed C is connected through an automatic valve 62 to a point in this second gas flow path between the automatic valves 60 A and 60 B. The system further comprises a product outlet 66 and an output conduit for coupling the gas outlets of the adsorption beds to the product outlet 66 In the 10 system shown the output conduit is connected to the said first flow path at a point between the flow control valves 50 A and 50 B and includes a first section 70 including an automatic valve 72 and a second section 74 including the series combination of a pressure regulator 76, a throttle valve 78 and a flow meter 80 The flow rate of product to the product outlet 66 is controlled by the throttle valve 78 15 which preferably is a manually adjustable needle-type valve, and the flow rate is indicated visually by the meter 80.
The system further comprises a reservoir 84 which functions primarily to store product gas received through a conduit 86 and to serve as a reserve supply of product for maintaining output in the event of a system malfunction 20 A first reservoir conduit is connected at one end to the second section 74 of the above-mentioned system output conduit and at the other end to an outlet conduit 86 of the reservoir 84 and includes flow control means in the form of check valve 90 which allows gas flow only in the direction from the system output conduit 74 to the reservoir 84 Another valve 92, in the form of a throttle valve which 25 preferably is manually adjustable, is connected in the conduit, preferably between the check valve 90 and reservoir 84 The valve 92 can be used to control the rate of flow of gas product, into reservoir 84.
A second reservoir conduit is connected at one end to reservoir 84 through conduit 86 and at the other end to the system output conduit and includes a valve 30 96 for controlling the flow of product gas from reservoir 84 to the output conduit section 74 A control unit 100 is connected by lines 102 and 103 to valves 72 and 96, respectively, and functions to open the normally-closed valve 96 in response to closing of valve 72 A pressure indicator meter 104 can be connected to the output of reservoir 84 for indicating the pressure of gas product remaining therein 35 In general, the present invention is illustrated in terms of a process and system utilising a first adsorption bed A, a second adsorption bed B and a segregated storage adsorption bed C, but can employ more than one first adsorption bed, more than one second adsorption bed and more than one segregated storage adsorption bed provided the first and second adsorption beds communicate with the feed gas 40 stream which supplies the gaseous mixture, and the segregated storage adsorption bed is never directly communicated with, or directly exposed to, the feed gas stream.
Although the process and system of the present invention are described with particular reference to fractionation of air to provide high purity oxygen product 45 gas by removal of nitrogen, essentially any gas mixture may be separated by the process and system of the present invention by the proper selection of the time for each cycle and step, and by the selection of a proper adsorbent material, adsorbent materials or mixtures of adsorbent materials.
As used herein, depressurising or depressurisation refers to the reduction of 50 pressure in the vessel and associated piping of an adsorption bed, and the level to which pressure is reduced can be selected by those skilled in the art depending upon operating conditions and the nature of the gas mixture being fractionated.
Desorption and purging pressures are selected in a similar manner Pressurising or pressurisation refers to the increase of pressure in the vessel and associated piping 55 of an adsorption bed The system illustrated has the capability of product gas delivery in a range of pressures down to about 2 p s i g and up to about 40 p s i g.
For example, in the fractionation of air to deliver high purity oxygen gas product, a delivery pressure of around 3 p s i g is employed for medical uses and breathing devices, whereas a higher delivery pressure of up to about 40 p s i g is ideally suited 60 for commercial uses such as in metal cutting or welding equipment.
Figure 2 illustrates a process timing sequence to enable the system of Figure 1 to be used for carrying out the present invention In Figure 2 the preferred times in seconds are indicated for each step, and the preferred pressures in each adsorption bed for each step are shown parenthetically and given in pounds per square inch 65 1,593,539 4 1,593,539 4 gauge The particular operation carried out in each adsorption bed during each step is shown in Figure 2 and most are abbreviated for concurrence in illustration.
Thus "FEE" refers to feed end equalisation (to be explained in further detail presently), "ISOL" refers to isolation of a particular adsorption, "EQ" refers to pressure equalisation of two adsorption beds (to be explained in further detail 5 presently), "REP" refers to repressurisation or repressurising to increase the pressure in an adsorption bed, and "PURGE" refers to introduction of purge gas or purging.
Prior to step I the gaseous mixture (i e atmospheric air) from the feed gas conduit 10 has been flowing through valve 40 A into and through adsorption bed A 10 wherein nitrogen is adsorbed High purity oxygen gas leaves bed A through outlet and flows through the open valve 54 and flow control valve 50 A and then along the first conduit section 70 through the open valve 72, along second conduit section 74 and through the series combination of pressure regulator 76, needle valve 78 and flow meter 80 to the product outlet 66 for use 15 Just prior to the beginning of step 1, adsorption bed A will be about saturated and nearing the end of the adsorption operation therein Also just prior to the beginning of step 1, the adsorption bed A is at a higher pressure than the adsorption beds B and C.
At the beggining of step 1, valve 40 B is opened, while valve 40 A and valve 72 are 20 kept open As indicated in Figure 2, at the beginning of step 1, typical pressures in beds A, B and C are 30, 7 and 7 p s i g respectively.
During step 1, gas flows from the bottom or feed end of bed A out through inlet 18 and in reverse direction through valve 40 A whereupon it mixes with the incoming feed air stream from conduit 10 and flows through valve 40 B into the 25 bottom or feed end of bed B Bed A is very near the end of the adsorption step therein so the composition of this gas withdrawn from inlet 18 thereof is not appreciably different from the composition of air As a result, during step 1, adsorption bed A is depressurised countercurrently to feed flow, and becomes pressure equalised with adsorption bed B causing the pressure in bed B to rise Also 30 in step 1, adsorption bed A continues to supply oxygen gas product, as the pressure reduces, but this is terminated by the end of the step which preferably has a duration of about 7 seconds Throughout step 1, and all other steps, there is continuous air flow into the system in conduit 10 and continuous product flow out through outlet 66 35 Step 1 may be described as continuing to discharge product gas from the outlet of the first bed A while simultaneously equalising the pressures of the first and second adsorption beds A and B from the feed ends thereof.
At the transition betweenwthe end of step I and beginning of step 2, as shown in Figure 2, the pressures in beds A and B are equalised at 20 p s i g and the pressure 40 in the segregated storage adsorption bed C has remained at 7 p s i g.
At the beginning of step 2, valve 40 B remains open, but valve 40 A closes, and valve 60 A opens No product gas is now obtained from adsorption bed A During this step, feed air continues to flow into the feed inlet 26 of bed B, and oxygen-rich gas is taken as product from the outlet 28 bed B and flows through flow control 45 valve 50 B into second conduit section 70 and to the product outlet 66 At the same time, reduced purity product gas flows from the outlet 20 of bed A through the valve 60 A and valve 62 and into the segregated storage adsorption bed C As a result, during step 2 adsorption bed A is pressure equalised with the segregated storage adsorption bed C 50 The automatic valve 62 can either remain open during all steps or be opened and closed when necessary.
Step 2 preferably has a duration of about 7 seconds.
The process of step 2 may be described as simultaneously terminating the pressure equalisation of step 1, adsorbing the gaseous mixture from the feed gas 55 stream in the second adsorption bed B, releasing product gas from the outlet of the second adsorption bed, and equalising the pressures of the first adsorption bed A and the segregated storage adsorption bed C.
At the transition between the end of step 2 and the beginning of step 3, as shown in Figure 2, the pressures in adsorption beds A and C are equalised at 14 p s i g and 60 the pressure in adsorption bed B has risen to 28 p s i g.
At the beginning of step 3, valve 40 B remains open, valve 60 A closes and valve 46 A opens During step 3 feed air continues to enter bed B, and product quality oxygen-rich gas continues to be taken as product from the outlet of bed B and is available at product outlet 66 Also during step 3, adsorption bed A is depressurised 65 to the atmosphere through valve 46 A and waste outlet 44 in a direction countercurrent to feed flow As a result, nitrogen rich waste gas is rejected to the atmosphere, and the pressure in bed A drops from 14 p s i g to 0 p s i g.
Simultaneously with the foregoing depressurisation, a portion of the oxygen gas product flowing from bed B through flow control valve 50 B will flow through valve 5 A and valve 54 into bed A The product quality oxygen gas flows through bed A in a direction opposite to that prevailing during air separation to give an oxygen purge flowing countercurrent to feed flow displacing nitrogen from the adsorbent material in bed A to become a nitrogen-rich stream leaving the system to the atmosphere through valve 46 A and outlet 44 Step 3 preferably has a duration of 10 about 39 seconds.
The process of step 3 may be described as simultaneously terminating the pressure equalisation of step 2, continuing adsorption, in the second adsorption bed B, of the gaseous mixture from the feed gas stream releasing product gas from the outlet of the second adsorption bed B, and depressurising the first adsorption bed 15 A (in a direction countercurrent to feed flow) and purging the first adsorption bed by diverting some product gas from the outlet of the second adsorption bed B into the first adsorption bed A in a direction countercurrent to feed flow.
At the transition between the end of step 3 and the beginning of step 4, as shown in Figure 2, the pressure in bed A is at 0 p s i g, the pressure in segregated 20 storage adsorption bed C has remained at 14 p s i g and the pressure in bed B has risen to 30 p s i g At the beginning of step 4, valve 40 B remains open, valve 46 A closes, and valve 60 A opens Valve 62, if not already open, is opened at the beginning of step 4 During step 4 feed air continues to enter bed B, and product quality oxygen gas continues to be taken as product from the outlet of bed B and 25 is available at product outlet 66 At the same time, gas flows from the segregated storage tank C, through valves 62 and 60 A, into bed A through the outlet 20 thereof This gas withdrawn from adsorption bed C during step 4 is a version of the gas supplied to bed C during step 2 which gas has been influenced by its travel into and out of bed C 30 As a result, during step 4 the segregated storage adsorption bed C-is pressure equalised with the adsorption bed A At least during the initial portion of step 4, there may be some additional flow of purge gas from bed B through valves 50 B, A and 54.
Step 4 preferably has a duration of about 7 seconds 35 The process of step 4 may be described as simultaneously terminating the depressurising and purging of the first adsorption bed A, continuing adsorption of the gaseous mixture from the feed gas stream in the second adsorption bed B, releasing product gas from the outlet of the second adsorption bed B and equalising the pressures of the segregated storage adsorption bed C and the first adsorption 40 bed A.
The foregoing process steps 1, 2, 3 and 4 are repeated consecutively, reversing the functions of the adsorption beds A and B beginning with pressure equalisation of the adsorption beds A and B from the feed ends thereof At the transition between the end of step 4 and the beginning of step 5, as shown in Figure 2, the pressures in 45 beds A and C are equalised at 7 p s i g and the pressure in bed B has remained at 30 p.s i g.
At the beginning of step 5, valve 40 B remains open, valve 60 A closes and valve A opens During this step, gas flows from the bottom or feed end of bed B, which is near the end of its adsorption operation, in a reverse direction through valve 40 B 50 whereupon it mixes with the incoming feed air stream from conduit 10 and the resulting mixture flows through valve 40 A into the bottom or feed end of bed A As a result, adsorption bed B becomes pressure equalised with adsorption bed A, and bed A begins to adsorb the feed gas mixture This feed end equalisation is similar to that which occurred during step I but in this step the roles of the beds A and B are 55 interchanged Also during step 5, while the pressure in bed B is falling during feed end equalisation, product quality oxygen-rich gas continues to be taken as product from bed B and is available at product outlet 66 This step begins the second half of the process cycle wherein steps 5 to 8 are similar to 1 to 4 with the roles of beds A and B interchanged and with the valve sequence being the same but with the A and 60 B designations interchanged.
The process of step 5 may be described as simultaneously terminating the pressure equalisation of step 4, continuing to discharge product gas from the outlet of the second adsorption bed B while simultaneously equalising the pressures of the second and first adsorption beds B and A, respectively, from the feed ends thereof 65 s 1,593,539 by withdrawing gas from the feed inlet of the second adsorption bed B at the end of the adsorption operation therein in a direction countercurrent to feed flow and introducing the withdrawn gas along with the gaseous mixture from the feed gas stream to the feed inlet of the first adsorption bed A in a direction cocurrent with feed flow and after pressurisation thereof 5 Carrying out the pressure equalising of the adsorption beds A and B at the feed ends thereof, as illustrated in step 1, advantageously reduces energy requirements and increases oxygen recovery When an adsorption bed, at the end of the adsorption step therein, is depressurised countercurrently to feed flow, i e as bed A from 30 p s i g to 20 p s i g in step I, the composition of the gas obtained from 10 the bed inlet is not greatly different from air and this gas can therefore be introduced into the feed end of an adsorbent bed in a repressurising phase without any appreciable loss in system performance as compared with the more usual step of repressurising using only the air from the system compressor 12 Feed end equalisation allows the repressurisation of one bed to be assisted cocurrently by the 15 depressurisation air from another bed and thus greatly reduces the feed air requirement and increases oxygen recovery, i e decreases the size of compressor 12 required to produce a given amount of oxygen and to achieve the required rapid repressurisation for maintaining near constant output pressure Feed end equalisation recovers energy, increases system efficiency and can be used for both 20 low and high product delivery pressures The foregoing advantages of course apply to both of the feed and equalisationswhich occur during a single cycle as illustrated in steps 1 and 5.
Feed end equalisation requires less adsorbent material in a given bed as compared to product end equalisation, for the following reasons In product or 25 outlet end equalisation, the bed at the higher pressure depressurises in a direction cocurrent to feed flow during the pressure equalisation step This causes the mass transfer zone to advance toward the product end of the bed as the pressure decreases In order to contain the mass transfer zone during this step to maintain product purity, a larger bed, i e a greater quantity of adsorbent material, is 30 required In feed end equalisation, on the other hand, the bed at the higher pressure depressurises in a direction countercurrent to feed flow during the equalisation step In this step, due to the direction of the gas flow, the mass transfer zone does not advance The countercurrent depressurisation is also beneficial for the subsequent purge step because nitrogen starts to flow toward the feed end of 35 the bed during this step The combination of no advancing of the mass transfer zone and countercurrent depressurisation reduces the amount of adsorbent material required.
Bed size factor is a quantity used to compare the amount of adsorbent material required from one system or cycle to another At a given bed size factor, it has been 40 determined that using feed end equalisation produces oxygen at a higher purity as compared to using product end equalisation.
The combination of equalising pressures between an adsorption bed and the segregated storage adsorption bed, when the adsorption bed is at the end of the adsorption operation therein and prior to purging of the bed as illustrated in step 2, 45 and thereafter equalising pressures between these same two components after purging of the adsorption bed, when it is at a relatively low pressure as illustrated in step 4, maximises the utilisation of the adsorption bed while at the same time maximizing purity of the product In particular during step 2, as the depressurising bed A equalises cocurrently to feed flow into the segregated storage adsorption bed 50 C, part of the nitrogen contained in the mass transfer zone of bed A will be transferred into the bed C This allows for maximum and continuous utilisation of bed A, i e the mass transfer zone can be moved along bed A from inlet to outlet as far as possible At the beginning of the flow from bed A to bed C the gas is rich in oxygen but as flow continues the gas gradually 55 reverts to the composition of fresh air In additon, the segregated storage adsorption bed recovers some potential energy from the depressurising adsorber and this, in turn, reduces system blow-down pressure and increases recovery and efficiency Providing the segregated storage adsorption bed C in effect provides a mixing volume to smooth out any fluctuations in product 60 purity which otherwise might occur when the front of the mass transfer zone breaks out of the output end of an adsorption bed The foregoing advantages result when the system is operating at equilibrium conditions and at flow conditions for which the system is optimally designed For example, When the system is used to supply 1,593,539 7 1,593,539 7 oxygen for medical use, design conditions occur at a flow rate of about 30 litres per minute.
During step 4, as the segregated storage adsorption bed C pressureequalises countercurrently to feed flow into bed A, the gas returned to bed A is dispersed therethrough in a manner which does not adversely affect product purity The gas 5 is not returned to adsorber A in a lump quantity concentrated in the output region of bed A but instead is dispersed through and along the bed A The foregoing is believed to result from the fact that gas return to bed A occurs immediately after.
purging, when its pressure is relatively low, i e 0 p s i g, this low pressure allowing the gas to disperse readily through the bed It is believed that low or zero pressure 10 in bed A at the beginning of the repressurising from segregated bed C allows the incoming gas to move rapidly along the bed in a manner such that the adsorbent material adjacent the outlet end of the bed does not take up a large amount of nitrogen At the beginning of gas flow from bed C to bed A, the gas is rich in nitrogen but as the flow continues it becomes more rich in oxygen The foregoing 15 advantages are of course equally evident as bed C pressure equalises with the second bed B during steps 6 and 8.
Providing flow control valves 50 A and 50 B allows the system to be balanced by providing individual adjustment of the purge gas flow to each of the adsorption beds A and B Providing an adjustable flow control valve associated with each of 20 the two beds permits compensating for differences in the beds and in piping by simple manual adjustment of t He respective valves 50 A and 50 B An unbalanced system is characterised by the front of the mass transfer zone breaking through the output end of one bed sooner than in the other bed In order to maintain product purity, this would limit system operation to the "time to breakthrough" of that bed 25 which is first to experience nitrogen breakthrough thereby causing the other bed to be under-utilised with the result that the entire system produces less oxygen at a given purity Although, as illustrated in Figure 1, the product gas may also travel through these same valves toward the system product outlet 66, the doubleacting flow control valves 50 A and 50 B (i e allowing free flow one way and controlled 30 reverse flow) could be replaced by two simple needle valves for independently controlling purge flow and then two check valves would be connected in parallel with the needle valves each being polarised to transmit product gas from the bed outlets to the system product outlet 66.
The automatic valve 54 (left open throughout steps I to 8) in the path 35 containing valves 50 A, 50 B is a shut down isolation valve which serves to isolate beds A and B when the system is shutdown to maintain-the respective pressures in the beds and prevent pressure equalisation When the system is shut down, all the other automatic valves also close Then when' the system is again placed in operation, less time is required to reach desired operating conditions by virtue of 40 the beds A and B having been maintained at their respective pressures prior to shut down.
Table I presents data illustrating the effect of the segregated storage tank or segregated storage adsorption bed C on system performance The data presented in Table I is for oxygen product at a purity of 90 % and the oxygen recovery 45 percentage is presented for both low pressure and high pressure delivery conditions The abbreviations used are: S S T for segregated storage tank and F.E E for feed and equalisation.
TABLE I
Low High 50 Pressure Pressure Delivery Delivery S.S T Absent 21 % 21 % S.S T Present 25 % 23 % But Empty 55 S.S T Half Full 35 % 31 % Of Adsorbent Material S.S T Full and 49 % 48 % With F E E.
Figure 3 shows a detail of another embodiment of a system according to the 60 present invention wherein gas product can be withdrawn from the other end of the segregated storage adsorption bed C In the system shown in Figure 3, any components identical to those of Figure 1 have the same reference numerals but primed The system, only a detail of which is shown in Figure 3 would of course also include adsorption beds A' and B' (not shown) identical to those designated A and B in the system of Figure 1, along with similar connections to the gas inlets and outlets, the gas feed stream, waste outlet, and product output.
The end of the segregated storage adsorption bed C' opposite its inlet 34 ' is 5 connected by a conduit 108 which contains an automatic valve 110 to the second output conduit section 74 upstream from regulator 76 ' Upon opening of valve 110, product quality gas can be withdrawn from the segregated storage adsorption bed C' and introduced to the output conduit and this can be advantageous in situations where low pressure rather than high pressure product delivery is needed In 10 addition, when product is delivered from the segregated storage adsorption bed C', the bed serves also as a product surge tank enabling product to be withdrawn from the system at a high flow rate for a short period of time before the mass transfer zone breaks through that end of the bed On the other hand, recovery from a breakthrough condition can be relatively slow Another advantage of withdrawing 15 product gas from the segregated storage bed C' is that it provides a relatively higher rate of recovery of product This is because withdrawal of product from storage bed C' reduces the pressure therein so that when the pressure next equalises with either of the adsorption beds A' and B' that adsorption bed will be at a lower pressure The lower pressure, in turn, imposes a lower blow-down requirement for 20 purging that adsorption bed with a result that less gas is released to the atmosphere.
This reduction in the waste losses results in a higher percentage of product recovery Another advantage associated with the double-connected segregated storage bed C' involves feed end equalisation which lowers the front of the mass transfer zone in each of the other two beds A' and B' so that when the beds are 25 equalised from the tops with the segregated storage bed C' there is less nitrogen to be taken up by the segregated storage adsorption bed.
As shown in Figure 3, the system can also include a third reservoir conduit 114, connected at one end to the reservoir 84 ' and coupled at the other end to the adsorption beds In the present illustration, the "bed" end of conduit 114 is 30 connected to the flow path containing the automatic valves 60 A' and 60 B' and is connected between these valves Conduit 114 contains an automatic valve 116 which, upon opening, allows product gas from reservoir 84 ' to flow to the adsorption beds to be used for operations such as purging and repressurisation.
The primary role of the reservoir in the systems of Figures 1 and 3 is to hold a 35 reserve supply of product gas in the event of equipment malfunction or power failure This is of particular importance when the system supplies oxygen for medical use Under normal operating conditions the reservoir is at a pressure of 28-29 p s i g, and product oxygen flows through valve 72 and regulator 76 to product outlet 66 If electrical power fails or is otherwise interrupted the valve 72 40 closes and this is sensed by control 100 which will open valve 96 Oxygen flow continues from the reservoir through valve 96 to the output conduit to outlet 66 until the supply in the reservoir is depleted An alarm can be sounded to indicate the power interruption.
The reservoir also can be used to supply part or all of the purge oxygen 45 required, for an adsorption bed during its purge step, simply by opening valve 116 at the appropriate time The reservoir also can be used as another surge tank.
Pressure equalisations to and from the adsorption beds can be accomplished through the correct sequencing of valves 116 and 62.
When the reservoir is supplying reserve oxygen, in the event of a malfunction, 50 the length of time the reserve oxygen lasts depends on the pressure in the reservoir at the time of the malfunction If the reservoir is only ever used as a back-up oxygen supply, the reservoir pressure will be at its maximum at all times, whereas if the reservoir is used to supply supplemental purge and/or repressurisation gas, the pressure in the reservoir will vary as will the reserve supply of oxygen The 55 reservoir can comprise an adsorption bed but it also can comprise an ordinary tank of larger size.
Figure 4 shows an arrangement for controlling the system of Figure I or 3 The output conduit 74 ' can be connected to a tank or similar storage vessel 120, and gas product can be withdrawn therefrom through a conduit 122 for use The 60 sequencing and timing of the system including the control of the automatic valves is achieved by a system control unit designated 124, and control signals generated by the control unit 124 are transmitted by lines collectively designated 126 to the valves and other appropriate components of the system Generally, the control 124 is responsive to the pressure of product gas within the storage vessel 120, and to this 65 I 1,593,539 end a pressure sensor 130 is operatively connected to the storage vessel 120 by the connection 132 The output from sensor 130 is connected by a line 134 to an additional control unit 136 which, in turn, is connected in controlling relation to the system control unit 124 by the connection 138 It has been determined that once operation of the system has begun there is an optimum time at which to terminate 5 operation, both in terms of a minimum number of cycles to be completed and a point within a cycle to terminate operation The additional control unit 136 functions to cause the system control unit 124 to ignore any "shut-down" signal and to maintain operation of the system, once begun, for a predetermined number of cycles It has been determined that, in a system for producing oxygen from feed air, 10 a total of two complete cycles provides desirable results One complete cycle includes steps 1 to 8 tabulated in Figure 2 Furthermore, it has been determined that there is an optimum point within a cycle at which operation of the system should be terminated, and this will be when the pressures are equal in the two adsorption beds A and B, i e at the beginning of step 2 or step 6 Thus, the 15 additional control unit 136 also functions to ignore any shut-down signal and to stop the system only after two complete cycles have been completed and only at an optimum point within the next following cycle when the pressures are equal in the two adsorption beds A and B The additional control unit 136 can, for example, be of the cam type or step switch type Thus, the system control unit 124 is responsive 20 to gas pressure in storage vessel 120, signalled by sensor 130, for stopping operation of the process and system normally when gas pressure in storage vessel 120 reaches a predetermined magnitude The additional control unit 136 thus overrides the system control unit 124 to terminate operation of the process and system only at a predetermined instant in the first cycle after the completion of the minimum 25 number of cycles as determined by system control unit 124.
Various aspects of the apparatus and process described above are also described and claimed in our co-pending Patent Applications Nos 49029/77 and 8002359 (Serial Nos 1593538 and 1593540, respectively).

Claims (16)

WHAT WE CLAIM IS: 30
1 A pressure swing adsorption process using at least one adsorption bed having a gas inlet and a gas outlet and at least one storage adsorption bed which is segregated from the gas inlet of said at least one adsorption bed and is able to be communicated with the gas outlet of said at least one adsorption bed, comprising the steps of flowing a feed gas mixture into said inlet of said at least one adsorption 35 bed to adsorb at least one gas of said mixture within said bed while flowing the remainder of said gas mixture out of said bed outlet as product gas until said adsorption bed is about saturated with said one gas and the purity of said product gas has reduced; flowing reduced purity product gas fromsaid bed outlet into said segregated storage adsorption bed by depressurising said at least one adsorption 40 bed into said segregated storage adsorption bed until the mass transfer zone within said adsorption bed moves into said segregated storage adsorption bed, closing the flow path between said adsorption bed and said segregated storage adsorption bed; purging said one bed in a countercurrent direction; and flowing gas from said segregated storage adsorption bed back into said adsorption bed by depressurising 45 said segregated storage adsorption bed and repressurising said purged at least one adsorption bed.
2 A process according to claim 1, wherein the withdrawn reduced purity product gas is introduced to only one end of said segregated storage adsorption bed as the sole gas introduced into said segregated storage adsorption bed; and gas is 50 withdrawn from said one end of said segregated storage adsorption bed and passed into said at least one adsorption bed in a direction countercurrent to feed flow after said desorption step, the feed end of said at least one adsorption bed being closed during such passage, whereby said gas aids in repressurising said at least one adsorption bed 55
3 A process according to claim 2, wherein after withdrawal of gas from the outlet of said at least one adsorption bed into said segregated storage adsorption bed, the flow path between said at least one adsorption bed and said segregated storage adsorption bed is closed and said at least one adsorption bed is purged by flow therethrough of a purging gas in a direction which is countercurrent to the 60 feed direction, before gas from said segregated storage adsorption bed is flowed back into said at least one adsorption bed to repressurise said at least one adsorption bed after purging.
4 A process according to claim 2 or claim 3, wherein the return of gas from I 1,593,539 said segregated storage adsorption bed into said at least one adsorption bed after purging takes place when that adsorption bed is at a relatively low pressure and the feed end of that adsorption bed is completely closed, whereby said returning gas repressurises that adsorption bed.
5 A process according to any one of the preceding claims, using each of at 5 least two said adsorption beds by sequentially passing the gaseous mixture from a feed stream through a first of said adsorption beds until the first bed is about saturated while simultaneously purging and then pressurising a second of said adsorption beds, and then passing the gaseous mixture from the feed stream through the second adsorption bed until the second bed is about saturated while 10 simultaneously purging and then pressurising the first adsorption bed, withdrawing reduced purity product gas from said first adsorption bed in a direction cocurrent with feed flow when said first adsorption bed is at the end of the adsorption operation therein and prior to purging of said first adsorption bed; introducing the withdrawn reduced purity product gas to only one end of said segregated storage 15 bed as the sole gas introduced into said segregated storage adsorption bed to move the mass transfer zone from said first adsorption bed into said segregated storage bed withdrawing gas from said one end of the segregated storage bed and passing said withdrawn gas into said first adsorption bed in a direction countercurrent to feed flow after purging of said first adsorption bed and when said first adsorption 20 bed is at a relatively low pressure, the feed end of said first adsorption bed being closed during such passage, whereby said gas starts repressurising said first adsorption bed; and then at the end of an adsorption phase in the second adsorption bed withdrawing gas from the outlet end thereof cocurrent with feed flow and into said segregated storage adsorption bed to move the mass transfer 25 zone from said second adsorption bed into said segregated storage adsorption bed and later returning gas from said segregated storage adsorption bed into said second adsorption bed to repressurise said second adsorption bed.
6: A process according to any one of the preceding claims, wherein after purging of said one adsorpton bed and partial repressurisation thereof with said 30 withdrawn gas returned to said one adsorption bed, product gas is withdrawn from the outlet end of said segregated storage adsorption bed and recovered directly without further treatment.
7 A process according to any one of the preceding claims, wherein the product gas is passed along a conduit system from said bed outlet to a product 35 delivery conduit communicating with a product gas reservoir, said process further comprising the steps of normally preventing flow of product gas out of said reservoir, and flowing product gas from said reservoir to said delivery conduit when normal gas flow in said conduit system from said bed to said delivery conduit ceases, whereby product gas continues to be delivered to said delivery conduit even 40 after failure of normal product gas flow, until such time as said reservoir is exhausted.
8 A process according to claim 7, wherein normal flow of product gas to said product delivery conduit is by way of a control valve which closes automatically in response to failure of the main power supply, and wherein flow of product gas from 45 said reservoir to said product delivery conduit is initiated automatically in response to closure of said automatic valve
9 A process according to claim 7 or 8, wherein there are two said adsorption beds with their outlets connected to a product outlet conduit by a conduit system.
10 A process according to claim 9, wherein said process comprises the steps of 50 alternately and sequentially flowing a feed gas mixture into the inlet of one of said beds to adsorb at least one gas in said mixture in said one bed and flowing the remainder of the mixture out of the outlet of said one bed as product gas until said one bed is about saturated with said one gas, purging a second of said adsorption beds while performing the adsorption step in said one bed, and controlling the 55 repetition to continue until an instant in the repetition, optimum for shut-down.
11 A process according to claim 10, wherein said optimum point is decided on the basis of both an optimum point during the cycle and the completion of a minimum number of complete cycles from start-up.
12 A process according to claim 11, wherein said minimum number of cycles 60 is 2.
13 A process according to claim 10, 11 or 12, wherein said continuation of the repetition terminates at an optimum point in the process, and said optimum point is at an instant when the pressures in the said at least two adsorption beds are equalised 65 1,593,539 lo
14 A process according to claim 5 or to any one of claims 9 to 13, wherein during adsorption on each of said first and second adsorption beds the feed gas mixture is flowed into the inlet end of one of the respective beds and product gas is flowed out of the outlet of said respective bed along an outlet conduit system in an unrestricted manner in a flow direction away from the bed and towards a main 5 product outlet conduit whereas during purging of said respective bed using product gas from the other of said first and second adsorption beds the flow of purging gas into the said respective bed passing along said outlet conduit system in a direction from the main product outlet conduit towards the respective bed is restricted.
15 A process according to claim 14, wherein said purging gas flow is restricted 10 using means for simultaneously and automatically restricting flow towards said respective bed but allowing unrestricted flow in a direction away from said bed and towards said main product outlet conduit.
16 A process according to claim 15, wherein said means for simultaneously and automatically restricting flow comprises (a) a first polarised flow control valve, 15 between the product gas outlet of said first adsorption bed and said second adsorption bed, designed to allow unrestricted gas flow in a direction from said outlet of said first bed toward said second adsorption bed but controlled flow in a direction towards said gas outlet of said first adsorption bed; and (b) a second polarised flow control valve, between the product gas outlet of said second 20 adsorption bed and said first adsorption bed, allowing unrestricted gas flow in a direction from said outlet of said second bed toward said gas outlet of said first adsorption bed but controlled flow in a direction toward said gas outlet of said second bed, the main product outlet conduit being connected to a location in the flow path of gas between said first and second polarised flow control valves 25 J A KEMP & CO, Chartered Patent Agents, 14, South Square, Gray's Inn,, London WC 1 R 5 EU.
Printed for Her Majesty's Stationery Office, by the Courier Press, Leamington Spa, 1981 Published by The Patent Office, 25 Southampton Buildings, London, WC 2 A l AY, from which copies may be obtained.
1 1 1 1 I 1.593,539
GB235880A 1976-11-26 1977-11-24 Pressure swing adsorption process for gas separation Expired GB1593539A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US74528576A 1976-11-26 1976-11-26

Publications (1)

Publication Number Publication Date
GB1593539A true GB1593539A (en) 1981-07-15

Family

ID=24996052

Family Applications (3)

Application Number Title Priority Date Filing Date
GB4902977A Expired GB1593538A (en) 1976-11-26 1977-11-24 Pressure swing adsorption process for gas separation
GB235880A Expired GB1593539A (en) 1976-11-26 1977-11-24 Pressure swing adsorption process for gas separation
GB235980A Expired GB1593540A (en) 1976-11-26 1977-11-24 Pressure swing adsorption process and system for gas separation

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB4902977A Expired GB1593538A (en) 1976-11-26 1977-11-24 Pressure swing adsorption process for gas separation

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB235980A Expired GB1593540A (en) 1976-11-26 1977-11-24 Pressure swing adsorption process and system for gas separation

Country Status (5)

Country Link
JP (1) JPS6022964B2 (en)
CA (1) CA1132918A (en)
DE (1) DE2752801A1 (en)
FR (3) FR2392706A1 (en)
GB (3) GB1593538A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2840357A1 (en) * 1978-09-16 1980-04-03 Linde Ag ADIABATIC ADSORPTION METHOD FOR GAS PURIFICATION OR SEPARATION
ZA871189B (en) * 1986-02-24 1987-11-25 Boc Group Inc Psa multicomponent separation tank equalization
JPS6428208A (en) * 1987-07-22 1989-01-30 Sumiyoshi Heavy Ind Equipment for production and supply of nitrogen gas
GB8812643D0 (en) * 1988-05-27 1988-06-29 Boc Group Plc Apparatus for separation of gas mixtures
DE3936781A1 (en) * 1989-11-04 1991-05-08 Draegerwerk Ag Pressure cycling gas adsorption system has selective throttles - in individual prod. gas outlets to common tank-supply conduit
JP5902920B2 (en) * 2011-11-10 2016-04-13 大陽日酸株式会社 Nitrogen gas production method, gas separation method and nitrogen gas production apparatus
JP6231363B2 (en) * 2013-11-26 2017-11-15 エア・ウォーター・ベルパール株式会社 Gas separation apparatus and method

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL278457A (en) * 1961-05-16
FR1426070A (en) * 1961-12-18 1966-01-28 Exxon Research Engineering Co Heatless adsorption process using pressure reduction and pressure equalization
US3306841A (en) * 1964-12-28 1967-02-28 Universal Oil Prod Co Gas separation process
DE1769936C3 (en) * 1968-08-08 1980-09-18 Union Carbide Corp., New York, N.Y. (V.St.A.) Adiabatic process for separating one or more components from gas mixtures
US3788036A (en) * 1972-07-26 1974-01-29 D Stahl Pressure equalization and purging system for heatless adsorption systems
US3880616A (en) * 1973-11-19 1975-04-29 Bendix Corp Respiratory support system

Also Published As

Publication number Publication date
GB1593540A (en) 1981-07-15
FR2454835B1 (en) 1982-12-10
DE2752801C2 (en) 1989-03-23
FR2454834A1 (en) 1980-11-21
CA1132918A (en) 1982-10-05
FR2392706B1 (en) 1984-07-27
FR2454835A1 (en) 1980-11-21
JPS6022964B2 (en) 1985-06-05
FR2454834B1 (en) 1986-01-31
DE2752801A1 (en) 1978-06-01
GB1593538A (en) 1981-07-15
FR2392706A1 (en) 1978-12-29
JPS5377878A (en) 1978-07-10

Similar Documents

Publication Publication Date Title
US4194890A (en) Pressure swing adsorption process and system for gas separation
US4263018A (en) Pressure swing adsorption process and system for gas separation
EP0008882B1 (en) Separation of multicomponent gas mixtures by pressure swing adsorption
EP0248922B1 (en) Process for producing oxygen-enriched gas
US4140495A (en) Turndown control for pressure swing adsorption
US3430418A (en) Selective adsorption process
US4428372A (en) Process and apparatus for providing breathing gas
CA2189232C (en) Method of recovering oxygen-rich gas
EP0932439B1 (en) Closed-loop feedback control for oxygen concentrator
US3564816A (en) Selective adsorption process
US3138439A (en) Apparatus and process for heatless fractionation of gaseous constituents
EP0705636A1 (en) Improved pressure swing adsorption process
US5707425A (en) Helium recovery from higher helium content streams
EP0067740A2 (en) Process and apparatus for improving gas recovery in a pressure swing adsorption system
US3977845A (en) Adsorptive process for selective separation of gases
CA2297590A1 (en) Single bed pressure swing adsorption process and system
AU662455B2 (en) The separation of gaseous mixtures
GB2086258A (en) Process and apparatus for separation of a gaseous mixture
EP0609620B1 (en) Gas separation
WO1995003873A1 (en) Method and apparatus for separating nitrogen-rich gas
JPH0263520A (en) Method and apparatus for separating oxygen from air
GB1593539A (en) Pressure swing adsorption process for gas separation
CA1335426C (en) Apparatus for the separation of gas mixtures
US4848985A (en) Separation of gas mixtures
GB2091121A (en) Separation of gas mixtures

Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee