US3119669A - Chemical process control - Google Patents
Chemical process control Download PDFInfo
- Publication number
- US3119669A US3119669A US95288A US9528861A US3119669A US 3119669 A US3119669 A US 3119669A US 95288 A US95288 A US 95288A US 9528861 A US9528861 A US 9528861A US 3119669 A US3119669 A US 3119669A
- Authority
- US
- United States
- Prior art keywords
- gas
- flow
- flow rate
- rate
- pair
- 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 - Lifetime
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B7/00—Halogens; Halogen acids
- C01B7/01—Chlorine; Hydrogen chloride
- C01B7/012—Preparation of hydrogen chloride from the elements
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B7/00—Halogens; Halogen acids
- C01B7/09—Bromine; Hydrogen bromide
- C01B7/093—Hydrogen bromide
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/12—Condition responsive control
Definitions
- Chemical processes such as the manufacture of HCl by the combustion of H with C1 and the manufacture of l-IBr by the combustion of H with Br are typical of processes which utilize gaseous reactants and manufacture gaseous phase products.
- one of the reactants be supplied in a precisely regulated fixed ratio with respect to the other, independent of the existing rate of product manufacture, which latter usually varies from zero to 160% based on the demand of nextfollowing downstream facilities.
- this invention consists of a method and apparatus for controlling the flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous phase product within the reactor, comprising, in order of operations effected in the direction running from the sources of supply of said pair of gases towards said reactor, sensing the flow of a first gas of said pair of gases and applying a signal representative of the rate of flow of said first gas to one side of an instantaneous gas flow rate ratio determination balance, sensing the flow of a second gas of said pair of gases and applying a signal representative of the rate of flow of said second gas to the other side of said gas flow rate ratio determination balance, removing gaseous product from the reactor, sensing the existing pressure of the gaseous product and controlling the rate of supply of said first gas to preserve substantially a predetermined value of existing pressure of the gaseous product, and independently deriving from said gas flow rate ratio determination balance a signalrepresentative of the existing ratio of flow of said second gas with respect to said first gas in control relationship of the rate of
- the combustion manufacture of HCl according to this invention is effected by burning hydrogen gas, supplied through the outer annular portion of conventional burner nozzle 10, in vaporous chlorine, supplied through the central pipe portion of the burner nozzle.
- Burner nozzle 10 is mounted vertically and centrally of a water-cooled upright reactor 11, provided at the top with an explosive pressure rupture disc 12, gaseous HCl being withdrawn as product through line 15 leading to downstream facilities not shown.
- the chlorine, supplied to the process through line 15, is arbitrarily considered tobe the first fluid, whereas the hydrogen, supplied to the process through line 17, is thus the second fluid, as these terms are employed in the appended claims.
- the chlorine flow rate varies from 02000 lbs./hr. of superheated (to about 35 C.) vaporous chlorine supplied at 40 p.s.i.g., the flow rate of which is controlled responsive to the commercial pneumatic flow rate transmitter indicated generally at 13, which operates in accordance with a sensed pressure drop across orifice 19 disposed in chlorine line 16. It is convenient to use pneumatic control equipment throughout, and this is indicated in block representation with control air inputs denoted by the letter A in all instances.
- the chlorine flow control valve denoted generally at 2%) is located downstream from transmitter 18 and is actuated by commercial type controller 21 as hereinafter described. Controller 21, as well as all of the controllers employed in the system detailed, is of the reverse-acting type, denoted by the letter R drawn in each individual controller block. Manual control of chlorine feed as well as the recording of the supply of this gas is effected by the flow recording control station 22 connected to transmitter 18 by a multiplicity of pneumatic lines, in this instance four in number, represented, however, as a single line 23 to simplify the showing.
- the control of supply of hydrogen parallels that of the chlorine, the hydrogen flow rate transmitter 27 being of the pneumatic type, obtaining its signal from orifice 28 mounted in hydrogen line 17.
- the hydrogen flow control valve is of conventional type, indicated generally at 29 located downstream from orifice 28, which is actuated by controller 30.
- Manual control of hydrogen feed as well as the recording of the supply of this gas is effected by flow recording control station 31, connected to transmitter 27 by a multiplicity of pneumatic lines, in this instance four in number, represented in single line convention at 32.
- volumetric gas flow rate ratio determination bridge employed in the system described herein was a Sorteberg Type D pneumatic force bridge 36 arranged for division such that the numerator is always smaller than the denominator. This, in conjunction with computing relay 40, hereinafter described, provides a signal proportional to instantaneous flow ratio of extremely high'sensitivity, i.e., the full scale ratio range for this application is typically 1.00:1 to 1.10:1.
- flow rate ratio bridge 36 receives its signal representative of chlorine flow through pneumatic line 37 running to flow rate transmitter 18, and its signal representative of hydrogen fiow through pneumatic line 38 running to flow rate transmitter 27.
- Ratio bridge 36 supplies the input through line 39 to a conventional type of computing relay 40, the reference pneumatic source for which is conventional pressure regulator 41, which is provided with its own pressure gage 42 on the output side.
- Hydrogen-to-chlorine flow ratio control is effected through commercial controller 44, receiving its input from computing relay 40 via pneumatic line 45 and transmitting its output via pneumatic line 46 to hydrogen controller 30.
- the hydrogen-to-chlorine flow ratio indication control station is indicated at 49, the controller for which has a pneumatic set for cascade control and a ratio range of 1.0:1 to 1.121.
- the HCl product gas pressure transmitter 50 is tapped into product discharge line 15 and, typically, has a range of -60 p.s.i.g. This provides the pneumatic signal input, via line 51, to HCl gas pressure controller 52.
- the output of the latter is a pneumatic input to high and low limit pneumatic relay 54 via line 53, which, in turn, applies the control reference input to chlorine controller 21 via line 55.
- the HCl pressure recording station is indicated generally at 56.
- the apparatus as hereinbefore described is completely operational and can be utilized without further equipment; however, due to variations in purity and density of the gaseous reactants and the small inherent error of the volumetric flow measuring devices hereinbefore described, measurement inaccuracies can result. It is, therefore, preferred to superimpose an independent control in the form of a product purity check, which can adjust the ratio of the reactants supplied to maintain a preselected product purity.
- a thermal conductivity analyzer 57 e.g., a Leeds & Northrup Co. Model 7802-D-A9-W17, adapted to measure the content of hydrogen (0-5% by volume range) in the HCl gas and generate an electrical control signal (0-20 mv.
- the installation hereinbefore described was provided with three HCl reactors discharging to a common header 65; however, in the testing operation detailed, one reactor was maintained in continuous standby and only two were kept in service at any one time.
- the pneumatic relay 54 for each reactor was set at a chlorine low limit flow rate control of 500 lbs/hr. and a high limit flow rate control of 1800 lbs./hr., and which proved entirely practicable.
- the chlorine flow rate is immediately measured by orifice 19 and the flow rate information obtained by transmitter 18, which delivers an output signal representative of the instantaneous rate of chlorine supply to one side of ratio determination bridge 36 and simultaneously to chlorine flow recording control station 22 via line 23.
- the hydrogen flow rate is measured by its own orifice 28 and the corresponding instantaneous fiow rate signal sent on by hydrogen flow transmitter 27 via line 38 to the other side of flow ratio determination bridge 36, and also to hydrogen flow recording control station 31 via line 32.
- Ratio determination bridge 36 operating through computing relay 40, delivers a continuous signal to the l1ydrogen-to-chlorine flow ratio control station 49 which, together with controller 44 connected in the same control loop therewith, resets the control point of hydrogen flow rate controller 30 via line 46, and thus adjusts valve 29 appropriately, so as to maintain at all times the 1*2 mol percent excess of hydrogen in the HCl product gas.
- the product HCl delivery pressure is continuously measured by HCl pressure transmitter 50, which indicates the instantaneous existing pressure at recording control station 56 and adjusts the set point of chlorine controller 21, adjusting valve 20 appropriately, via the control loop inclusive of controller 52,
- the hydrogen-in-I-ICl analyzer 57 is an optional auxiliary functioning entirely independent of the rest of the control apparatus. When used, this analyzer transmits a signal constituting a continual check on excess hydrogen content in the product via the control loop inclusive of hydrogen-in-chlorine recording station 62 and the associated controller 61 which, together, independently resets the control point of the hydrogen-tochlorine flow ratio controller 44 to compensate for product composition variations actually determined.
- the control system of this invention displays sufiiciently high inherent stability to make it possible to bring the manufacturing process to a steady level of operation within a relatively short period of time.
- Operational records obtained at recording stations 22, 31 and 56 revealed a surprisingly effective capability to adjust automatically to very large, instantaneous product demand changes.
- experience obtained over a relatively long period of sustained operation has demonstrated a very high reliability, which indicates that the control is a marked improvement over other methods now available to the art.
- this invention is not limited to combustion type reactions but, of course, is generally applicable to other types, including, specifically, catalystpromoted gas phase reactions.
- control is eifected on the basis of interrelationship between a given pair of gases, it will be clear that other reactants ingaseous liquid or solid phase can additionally be present, so long as the plan of control based on the two chosen gases is practicable for the over-all reaction involved.
- a method for controlling the flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor comprising, in order of operations effected in the direction running from the sources of supply of said pair of gases towards said reactor, sensing the flow of a first gas of said pair of gases and applying a signal representative of the rate of flow of said first gas to one side of a gas flow rate ratio determination balance, sensing the flow of a second gas of said pair of gases and applying a signal repre sentative of the rate of flow of said second gas to the other side of said gas flow rate ratio determination balance, removing gaseous product from said reactor, sensing the existing pressure of said gaseous product and controlling the rate of supply of said first gas to preserve substantially a predetermined value of said existing pressure, and independently deriving from said gas flow rate ratio determination balance a signal representative of the existing ratio of fiow rate of said second gas with respect to said first gas in control relationship of the rate of supply of said second gas thereby adjusting the flow rate of said second gas
- Apparatus for controlling the rate of flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor comprising in combination a gas flow rate ratio determination balance, means sensing the flow rate of a first gas of said pair of gases and transmitting a signal representative of the instantaneous rate or" flow of said first gas as one input to said gas flow rate ratio determination balance, means sensing the flow of a second gas of said pair of gases and transmitting a signal representative of the instantaneous rate of flow of said second gas as the other input to said gas flow rate ratio determination balance, means responsive to the existing pressure of the gaseous product delivered from said reactor inclusive of a flow-regulating valve disposed downstream from said means sensing the flow of said first gas of said pair of gases controlling the rate of supply of said first gas to preserve substantially a predetermined value of said existing pressure, and means responsive to said gas flow rate ratio determination balance inclusive of a flow-regulating valve disposed downstream from said means sensing the flow of said second gas of said pair of gases
- Apparatus according to claim 3 for controlling the rate of flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor, provided with analyzer means connected with sample intake in open communication with the product delivery outlet of said reactor subjecting said gaseous product to composition analysis, and means responsive to said analyzer means adjusting the set point of said gas flow rate ratio determination balance to restore said gaseous product to a predetermined composition level.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Flow Control (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Description
Jan. 28, 1964 R. F. LAIRD, JR, ETAL CHEMICAL PROCESS CONTROL Filed March 13, 1961 R .J s 2 RD E 0 M N UZEQEU Y TmU W N E Pm W S T 1 w A TL Hm V A RD United States Patent 3,119,69 CIEMICAL PROCESS CONTROL Robert F. Laird, Jr., Bridgeton, NJ, and David L. Wassum, Wilmington, Del., assignors to E. 1. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware Filed Mar. 13, 1961, Ser. No. 95,238 4 Claims. (Cl. 23232) This invention relates to a method and apparatus for chemical process control, and particularly to a method and apparatus for the control of a chemical process operating on gaseous reactants and producing a gaseous form product.
Chemical processes, such as the manufacture of HCl by the combustion of H with C1 and the manufacture of l-IBr by the combustion of H with Br are typical of processes which utilize gaseous reactants and manufacture gaseous phase products. For considerations of safety as well as product quality, it is usually imperative that one of the reactants be supplied in a precisely regulated fixed ratio with respect to the other, independent of the existing rate of product manufacture, which latter usually varies from zero to 160% based on the demand of nextfollowing downstream facilities. Moreover, it is desirable to obtain products at a steady, appreciably high, superatmospheric pressure, thus dispensing with downstream pumps and separate pressurized storage facilities. We have found, in addition, from experience with an I-lCl manufacturing system, that it is advantageous to conduct the combustion of gaseous phase reactants at substantial gage presures, because a more stable flame is thereby obtained, thus eliminating flame-out ditliculties as well as obtaining improved product quality.
The eifectuation of semi-automatic control as the resultant of a sensed product condition coupled with a type of proportioned ratio supply of reactants is taught in U.S.P. 2,909,413; however, operation is at near-atmospheric presure and, additionally, requires human intervention, particularly as regards the critical ratio control of reactants.
We have now found that it is possible to base control on product pressure solely or, if desired, on product pressure and product quality independently, which gives completely automatic control of a highly reliable nature. At the same time there is preserved freedom as regards human intervention, and there is obtained safe operation at steady appreciable gage pressures.
An object of this invention is to provide an improved method and apparatus for chemical process control which is, within reasonable limits, substantially independent of the pressure level of operation. Another object of this invention is to provide a method and apparatus for automatic chemical process control which has an extremely high reliability, quick response characteristics and a wide range of operational capability. The manner in which these and other objects of this invention are accomplished will become clear from the detailed description and the drawing, which is a schematic representation of a preferred control arrangement for the combustion manufacture of HCl according to this invention.
Generally, this invention consists of a method and apparatus for controlling the flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous phase product within the reactor, comprising, in order of operations effected in the direction running from the sources of supply of said pair of gases towards said reactor, sensing the flow of a first gas of said pair of gases and applying a signal representative of the rate of flow of said first gas to one side of an instantaneous gas flow rate ratio determination balance, sensing the flow of a second gas of said pair of gases and applying a signal representative of the rate of flow of said second gas to the other side of said gas flow rate ratio determination balance, removing gaseous product from the reactor, sensing the existing pressure of the gaseous product and controlling the rate of supply of said first gas to preserve substantially a predetermined value of existing pressure of the gaseous product, and independently deriving from said gas flow rate ratio determination balance a signalrepresentative of the existing ratio of flow of said second gas with respect to said first gas in control relationship of the rate of supply of said second gas by adjustment of the flow of said second gas of said pair of gases to preserve substantially a predetermined ratio of supply of said second gas with respect to said first gas.
Referring to the drawing, the combustion manufacture of HCl according to this invention is effected by burning hydrogen gas, supplied through the outer annular portion of conventional burner nozzle 10, in vaporous chlorine, supplied through the central pipe portion of the burner nozzle. Burner nozzle 10 is mounted vertically and centrally of a water-cooled upright reactor 11, provided at the top with an explosive pressure rupture disc 12, gaseous HCl being withdrawn as product through line 15 leading to downstream facilities not shown.
In the following description, the chlorine, supplied to the process through line 15, is arbitrarily considered tobe the first fluid, whereas the hydrogen, supplied to the process through line 17, is thus the second fluid, as these terms are employed in the appended claims. Typi cally, the chlorine flow rate varies from 02000 lbs./hr. of superheated (to about 35 C.) vaporous chlorine supplied at 40 p.s.i.g., the flow rate of which is controlled responsive to the commercial pneumatic flow rate transmitter indicated generally at 13, which operates in accordance with a sensed pressure drop across orifice 19 disposed in chlorine line 16. It is convenient to use pneumatic control equipment throughout, and this is indicated in block representation with control air inputs denoted by the letter A in all instances. The chlorine flow control valve denoted generally at 2%) is located downstream from transmitter 18 and is actuated by commercial type controller 21 as hereinafter described. Controller 21, as well as all of the controllers employed in the system detailed, is of the reverse-acting type, denoted by the letter R drawn in each individual controller block. Manual control of chlorine feed as well as the recording of the supply of this gas is effected by the flow recording control station 22 connected to transmitter 18 by a multiplicity of pneumatic lines, in this instance four in number, represented, however, as a single line 23 to simplify the showing.
The control of supply of hydrogen (typically furnished at a rate of 0-65 lbs/hr. at 40 p.s.i.g. and ambient temperature) parallels that of the chlorine, the hydrogen flow rate transmitter 27 being of the pneumatic type, obtaining its signal from orifice 28 mounted in hydrogen line 17. The hydrogen flow control valve is of conventional type, indicated generally at 29 located downstream from orifice 28, which is actuated by controller 30. Manual control of hydrogen feed as well as the recording of the supply of this gas is effected by flow recording control station 31, connected to transmitter 27 by a multiplicity of pneumatic lines, in this instance four in number, represented in single line convention at 32.
A rather precisely controlled excess of hydrogen must be maintained in the off gas from reactor 11, from the standpoint of both product quality and operating safety, and this is typically 1-2 mol percent. The volumetric gas flow rate ratio determination bridge employed in the system described herein was a Sorteberg Type D pneumatic force bridge 36 arranged for division such that the numerator is always smaller than the denominator. This, in conjunction with computing relay 40, hereinafter described, provides a signal proportional to instantaneous flow ratio of extremely high'sensitivity, i.e., the full scale ratio range for this application is typically 1.00:1 to 1.10:1.
As seen in the drawing, flow rate ratio bridge 36 receives its signal representative of chlorine flow through pneumatic line 37 running to flow rate transmitter 18, and its signal representative of hydrogen fiow through pneumatic line 38 running to flow rate transmitter 27. Ratio bridge 36 supplies the input through line 39 to a conventional type of computing relay 40, the reference pneumatic source for which is conventional pressure regulator 41, which is provided with its own pressure gage 42 on the output side. Hydrogen-to-chlorine flow ratio control is effected through commercial controller 44, receiving its input from computing relay 40 via pneumatic line 45 and transmitting its output via pneumatic line 46 to hydrogen controller 30. The hydrogen-to-chlorine flow ratio indication control station is indicated at 49, the controller for which has a pneumatic set for cascade control and a ratio range of 1.0:1 to 1.121.
The HCl product gas pressure transmitter 50 is tapped into product discharge line 15 and, typically, has a range of -60 p.s.i.g. This provides the pneumatic signal input, via line 51, to HCl gas pressure controller 52. The output of the latter is a pneumatic input to high and low limit pneumatic relay 54 via line 53, which, in turn, applies the control reference input to chlorine controller 21 via line 55. The HCl pressure recording station is indicated generally at 56.
The apparatus as hereinbefore described is completely operational and can be utilized without further equipment; however, due to variations in purity and density of the gaseous reactants and the small inherent error of the volumetric flow measuring devices hereinbefore described, measurement inaccuracies can result. It is, therefore, preferred to superimpose an independent control in the form of a product purity check, which can adjust the ratio of the reactants supplied to maintain a preselected product purity. Thus, there is provided a thermal conductivity analyzer 57, e.g., a Leeds & Northrup Co. Model 7802-D-A9-W17, adapted to measure the content of hydrogen (0-5% by volume range) in the HCl gas and generate an electrical control signal (0-20 mv. D.-C.) which is applied through the electrical conductor 58, shown in broken line convention in the drawing, to the electric-to-pneumatic potentiometer 59. The latter, in turn, supplies the pneumatic input via line 60 to the hydrogen-in-HCl analysis controller 61. The hydrogen in HCl recording station is denoted generally at 62 and the connection impressing independent control as a function of gas analysis is via line 63, furnishing a control reference input to the hydrogen-to-chlorine flow ratio controller 44.
In large scale operation it is necessary to utilize more than one burner-reactor, and this is accomplished by providing duplicate arrangements each identical with that described, which are individually provided with output lines 15, and 15", all discharging into a common header 65.
In one installation provided with three 2000 lbs/hr. each maximum capacity burners, it was necessary to produce high quality HCl for use in an organic chlorination process which operated at superatmospheric pressure and which, therefore, required a steady HCl product supply at p.s.i.g. regardless of the magnitude of demand for product. This was directly accomplished with the a};- paratus of this invention without resort to pumps or intermediate storage of any kind and, during sustained operation, it was ascertained that burner operation was at the same time substantially improved as regards both flame stability and also the combustion per se by the operation at higher pressure level. In this specific installa- 4 tion it was convenient to locate all instruments shown to the right of broken line 66 remote from the process on a common control room panel, and this was readily accomplished.
The installation hereinbefore described was provided with three HCl reactors discharging to a common header 65; however, in the testing operation detailed, one reactor was maintained in continuous standby and only two were kept in service at any one time. In order to safeguard against operation of the chlorine flow controller 21 at possibly unstable extremes of its range, the pneumatic relay 54 for each reactor was set at a chlorine low limit flow rate control of 500 lbs/hr. and a high limit flow rate control of 1800 lbs./hr., and which proved entirely practicable.
The chlorine flow rate is immediately measured by orifice 19 and the flow rate information obtained by transmitter 18, which delivers an output signal representative of the instantaneous rate of chlorine supply to one side of ratio determination bridge 36 and simultaneously to chlorine flow recording control station 22 via line 23.
The hydrogen flow rate is measured by its own orifice 28 and the corresponding instantaneous fiow rate signal sent on by hydrogen flow transmitter 27 via line 38 to the other side of flow ratio determination bridge 36, and also to hydrogen flow recording control station 31 via line 32.
The product HCl delivery pressure is continuously measured by HCl pressure transmitter 50, which indicates the instantaneous existing pressure at recording control station 56 and adjusts the set point of chlorine controller 21, adjusting valve 20 appropriately, via the control loop inclusive of controller 52,
As previously stated, the hydrogen-in-I-ICl analyzer 57 is an optional auxiliary functioning entirely independent of the rest of the control apparatus. When used, this analyzer transmits a signal constituting a continual check on excess hydrogen content in the product via the control loop inclusive of hydrogen-in-chlorine recording station 62 and the associated controller 61 which, together, independently resets the control point of the hydrogen-tochlorine flow ratio controller 44 to compensate for product composition variations actually determined.
The control system of this invention displays sufiiciently high inherent stability to make it possible to bring the manufacturing process to a steady level of operation within a relatively short period of time. Operational records obtained at recording stations 22, 31 and 56 revealed a surprisingly effective capability to adjust automatically to very large, instantaneous product demand changes. At the same time, experience obtained over a relatively long period of sustained operation has demonstrated a very high reliability, which indicates that the control is a marked improvement over other methods now available to the art.
It will be understood that this invention is not limited to combustion type reactions but, of course, is generally applicable to other types, including, specifically, catalystpromoted gas phase reactions. Moreover, while control is eifected on the basis of interrelationship between a given pair of gases, it will be clear that other reactants ingaseous liquid or solid phase can additionally be present, so long as the plan of control based on the two chosen gases is practicable for the over-all reaction involved.
From the foregoing, it is apparent that this invention can be modified in numerous respects without departure from its essential spirit, and it is intended to be limited only within the scope of the appended claims.
We claim:
1. A method for controlling the flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor, comprising, in order of operations effected in the direction running from the sources of supply of said pair of gases towards said reactor, sensing the flow of a first gas of said pair of gases and applying a signal representative of the rate of flow of said first gas to one side of a gas flow rate ratio determination balance, sensing the flow of a second gas of said pair of gases and applying a signal repre sentative of the rate of flow of said second gas to the other side of said gas flow rate ratio determination balance, removing gaseous product from said reactor, sensing the existing pressure of said gaseous product and controlling the rate of supply of said first gas to preserve substantially a predetermined value of said existing pressure, and independently deriving from said gas flow rate ratio determination balance a signal representative of the existing ratio of fiow rate of said second gas with respect to said first gas in control relationship of the rate of supply of said second gas thereby adjusting the flow rate of said second gas of said pair of gases in response to said signal of said fiow rate determination balance to preserve substantially a predetermined ratio of supply of said second gas with respect to said first gas.
2. A method for controlling the flow of a pair of gases introduced into a reactor according to claim 1 wherein said gaseous product is subjected to composition analysis, a signal is derived as a function of the existing composition of said gaseous product, and said signal is independently and additionally applied in control relationship of the set point of said gas flow rate ratio determination balance to bring said composition of said gaseous product to a predetermined level.
3. Apparatus for controlling the rate of flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor, comprising in combination a gas flow rate ratio determination balance, means sensing the flow rate of a first gas of said pair of gases and transmitting a signal representative of the instantaneous rate or" flow of said first gas as one input to said gas flow rate ratio determination balance, means sensing the flow of a second gas of said pair of gases and transmitting a signal representative of the instantaneous rate of flow of said second gas as the other input to said gas flow rate ratio determination balance, means responsive to the existing pressure of the gaseous product delivered from said reactor inclusive of a flow-regulating valve disposed downstream from said means sensing the flow of said first gas of said pair of gases controlling the rate of supply of said first gas to preserve substantially a predetermined value of said existing pressure, and means responsive to said gas flow rate ratio determination balance inclusive of a flow-regulating valve disposed downstream from said means sensing the flow of said second gas of said pair of gases independently controlling the rate of supply of said second gas to pre serve substantially a predetermined ratio of supply of said second gas with respect to said first gas.
4. Apparatus according to claim 3 for controlling the rate of flow of a pair of gases introduced into a reactor, which gases interact one with the other to form a gaseous product within said reactor, provided with analyzer means connected with sample intake in open communication with the product delivery outlet of said reactor subjecting said gaseous product to composition analysis, and means responsive to said analyzer means adjusting the set point of said gas flow rate ratio determination balance to restore said gaseous product to a predetermined composition level.
References Cited in the file of this patent UNITED STATES PATENTS 1,414,762 Townsend May 2 ,1922 2,697,652 Ribble et a1. Dec. 21, 1954 2,909,413 Hildyard Oct. 20, 1959
Claims (1)
1. A METHOD FOR CONTROLLING THE FLOW OF A PAIR OF GASES INTRODUCED INTO A REACTOR, WHICH GASES INTERACT ONE WITH THE OTHER TO FORM A GASEOUS PRODUCT WITHIN SAID REACTOR, COMPRISING, IN ORDER OF OPERATIONS EFFECTED IN THE DIRECTION RUNNING FROM THE SOURCES OF SUPPLY OF SAID PAIR OF GAES TOWARDS SAID REACTOR, SENSING THE FLOW OF A FIRST GAS OF SAID PAIR OF GASES AND APPLYING SIGNAL REPRESENTATIVE OF THE RATE OF FLOW OF SAID FIRST GAS TO ONE SIDE OF A GAS FLOW RATE RATIO DETERMINATION BALANCE, SENSING THE FLOW OF A SECOND GAS OF SAID PAIR OF GAES AND APPLYING A SIGNAL REPRESENTATIVE OF THE RATE OF FLOW OF SAID SECOND GAS TO THE OTHER SIDE OF SAID GAS FLOW RATE RATIO DETERMINATION BALANCE, REMOVING GASEOUS PRODUCT FROM SAID REACTOR, SENSING THE EXISTING PRESSURE OF SAID GASEOUS PRODUCT AND CONTROLLING THE RATE OF SUPPLY OF SAID FIRST GAS TO PRESERVE SUBSTANTIALLY A PREDETERMINED VALUE OF SAID EXISTING PRESSURE, AND INDEPENDENTLY DERIVING FROM SAID GAS FLOW RATE RATIO DETERMINATION BALANCE A SIGNAL REPRESENTATIVE OF THE EXISTING RATIO OF FLOW RATE OF SAID SECOND GAS WITH RESPECT TO SAID FIRST GAS IN CONTROL RELATIONSHIP OF THE RATE OF SUPPLY OF SAID SECOND GAS THEREBY ADJUSTING THE FLOW RATE OF SAID SECOND GAS OF SAID PAIR OF GASES IN RESPONSE TO SAID SIGNAL OF SAID FLOW RATE DETERMINATION BALANC E TO PRESERVE SUBSTANTIALLY A PREDETERMINED RATIO OF SUPPLY OF SAID SECOND GAS WITH RESPECT TO SAID FIRST GAS.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95288A US3119669A (en) | 1961-03-13 | 1961-03-13 | Chemical process control |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US95288A US3119669A (en) | 1961-03-13 | 1961-03-13 | Chemical process control |
Publications (1)
Publication Number | Publication Date |
---|---|
US3119669A true US3119669A (en) | 1964-01-28 |
Family
ID=22251178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US95288A Expired - Lifetime US3119669A (en) | 1961-03-13 | 1961-03-13 | Chemical process control |
Country Status (1)
Country | Link |
---|---|
US (1) | US3119669A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3411993A (en) * | 1965-02-08 | 1968-11-19 | Beckman Instruments Inc | Hydrogen detection |
US3992165A (en) * | 1974-02-01 | 1976-11-16 | International Materials Corporation | Fuel reformation system |
US4099962A (en) * | 1976-01-05 | 1978-07-11 | Grupo Industrial Alfa, S.A. | Method and apparatus for measuring and controlling the percentage reduction of ore in a moving bed gaseous reduction reactor |
US6036936A (en) * | 1996-06-28 | 2000-03-14 | Elf Atochem, S.A. | Process for the production of hydrogen bromide gas and device for its implementation |
US6355222B2 (en) * | 1997-12-12 | 2002-03-12 | Elf Atochem S.A. | Manufacture of hydrogen bromide gas |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1414762A (en) * | 1920-03-01 | 1922-05-02 | Hooker Electrochemical Co | Method of making hydrochloric acid |
US2697652A (en) * | 1950-05-22 | 1954-12-21 | Phillips Petroleum Co | Nitric acid plant and control system |
US2909413A (en) * | 1956-08-31 | 1959-10-20 | Hooker Chemical Corp | Method for regulating the flow of fluids to reactors |
-
1961
- 1961-03-13 US US95288A patent/US3119669A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1414762A (en) * | 1920-03-01 | 1922-05-02 | Hooker Electrochemical Co | Method of making hydrochloric acid |
US2697652A (en) * | 1950-05-22 | 1954-12-21 | Phillips Petroleum Co | Nitric acid plant and control system |
US2909413A (en) * | 1956-08-31 | 1959-10-20 | Hooker Chemical Corp | Method for regulating the flow of fluids to reactors |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3411993A (en) * | 1965-02-08 | 1968-11-19 | Beckman Instruments Inc | Hydrogen detection |
US3992165A (en) * | 1974-02-01 | 1976-11-16 | International Materials Corporation | Fuel reformation system |
US4099962A (en) * | 1976-01-05 | 1978-07-11 | Grupo Industrial Alfa, S.A. | Method and apparatus for measuring and controlling the percentage reduction of ore in a moving bed gaseous reduction reactor |
US4153450A (en) * | 1976-01-05 | 1979-05-08 | Grupo Industrial Alfa, S.A. | Method and apparatus for measuring and controlling the percentage reduction of ore in a moving bed gaseous reduction reactor |
US6036936A (en) * | 1996-06-28 | 2000-03-14 | Elf Atochem, S.A. | Process for the production of hydrogen bromide gas and device for its implementation |
US6355222B2 (en) * | 1997-12-12 | 2002-03-12 | Elf Atochem S.A. | Manufacture of hydrogen bromide gas |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2072384A (en) | Method of and apparatus for proportioning combustible fluids | |
US3594557A (en) | Method for the automatic control of a process variable | |
US5288149A (en) | Gas calorimeter and wobbe index meter | |
US3963043A (en) | Pressure sensing method and apparatus for gases | |
US3119669A (en) | Chemical process control | |
US2689932A (en) | Balanceable network electric measuring system | |
US4080434A (en) | Method for control of carbon black reactor | |
US3725653A (en) | Apparatus for controlling chemical processes | |
US3174298A (en) | Process controller | |
US3894832A (en) | Heat-input-controlled gas-fired equipment and method | |
US3754125A (en) | Vent gas control system | |
US3771940A (en) | Smokeless gas flare with specific gravity gas analyzer for reducing noise | |
US2228315A (en) | Gas-delivery apparatus and method | |
US3211372A (en) | Combustion-control system | |
US2973772A (en) | Controller limit system | |
US2702238A (en) | Apparatus for controlling synthesis reactions | |
US20120092950A1 (en) | Low pressure drop blender | |
US2542905A (en) | Apparatus for measuring pressure | |
US3273348A (en) | Process and apparatus for preparing gaseous mixtures | |
US3783684A (en) | Fuel gas flow-meter corrector equipment for gases having variable characteristics | |
GB850087A (en) | System for regulating the flow of fluids to reactors | |
US2169175A (en) | Method of and apparatus foe con | |
US2285287A (en) | Automatic control apparatus | |
US2915079A (en) | Air-pressure-operated proportional band adjustment | |
US3357255A (en) | Fluid pressure system leak detector |