US1840186A - Method of controlling reactions - Google Patents

Method of controlling reactions Download PDF

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Publication number
US1840186A
US1840186A US277383A US27738328A US1840186A US 1840186 A US1840186 A US 1840186A US 277383 A US277383 A US 277383A US 27738328 A US27738328 A US 27738328A US 1840186 A US1840186 A US 1840186A
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Prior art keywords
bath
steam
controlling
molten
water
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Expired - Lifetime
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US277383A
Inventor
Robert P Courtney
Virgil E Meharg
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Bakelite Corp
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Bakelite Corp
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Priority to US277383A priority Critical patent/US1840186A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/06Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds in tube reactors; the solid particles being arranged in tubes
    • B01J8/067Heating or cooling the reactor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00026Controlling or regulating the heat exchange system
    • B01J2208/00035Controlling or regulating the heat exchange system involving measured parameters
    • B01J2208/00044Temperature measurement
    • B01J2208/00053Temperature measurement of the heat exchange medium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00026Controlling or regulating the heat exchange system
    • B01J2208/00035Controlling or regulating the heat exchange system involving measured parameters
    • B01J2208/00079Fluid level measurement
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00106Controlling the temperature by indirect heat exchange
    • B01J2208/00168Controlling the temperature by indirect heat exchange with heat exchange elements outside the bed of solid particles
    • B01J2208/00212Plates; Jackets; Cylinders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/0053Controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling

Definitions

  • This invention relates to methods of controlling exothermic reactions of the type requiring a comparatively close heat regulation at temperatures decidedly above that of boiling water. Without thereby limiting our invention we will describe the same by reference, as a specific illustrative example, to the manufacture of formaldehyde by the catalytic oxidation of methanol at a temperature i0 approximating 350 C.
  • the reaction vessel in tubular or other form, is surrounded by a bath of a molten salt or salts at the appropriate temperature.
  • a molten salt or salts at the appropriate temperature.
  • We accomplish both of these objects by injecting directly into the molten bath a spray of a liquid which is readily volatizable at the reacting temperature.
  • Fig. 1 is a front elevation with the end portions in section on the line 1-1 of Fig. 2,
  • Fig. 2 is an end view of the apparatus shown in Fig. 1;
  • Fig. 3 is a front elevation of the lower end of the saline bath receptacle of Fig. 1 with the front wall of said receptacle broken away.
  • 1 is the saline bath receptacle, being a -cylindrical tube.
  • 'lhe receptacle 1 carries end flanges 2, 2 and is provided with suitable thermometer wells 3, 3, 3, pet cocks 4, 4, 4 for adjusting the height of the saline bath, a vaived saline bath drain 5, and a superheated steam or vapor exit pipe 6.
  • the four spray jets 7, 7, 7, 7 marked Steam injector on Fig. 1 project through the wall of receptacle 1 1928.
  • a ring-shaped, perforated spray pipe 8 see Fig. 3, may be used.
  • the reaction tubes 9 in the apparatus illustrated are about 0.5 inch in diameter and about 30 inches long and are secured in headers 10, 10.
  • the tubes are filled with the catalyst 11, preferably in the form of spherical balls which assume an orderly arrangement.
  • the group of reaction tubes 9 is positioned within the receptacle 1 with the headers 10, 10 resting against the end flanges 2, 2, preferably with suitable copper-asbestos gaskets 12, 12 therebetween.
  • rEhe endsof the tubes 9 open into chambers 13, 13, formed by the tubular shells 14, 14, having flanges 15, 15 for attachment to flanges 2, 2, that is,vas illustrated flanges 14, 14 are bolted to flanges 2, 2 with the outer edges of headers 10, 10 clamped between them.
  • a perforated plate 17 serves to support the catalyst 11 in the tubes 9.
  • Chambers 13, 13 are provided with projecting conduits 16, 16 for connection to ⁇ a source of fluids, such as a mixture of methanol and air or oxygen, to be treated and to apparatus, such as a condenser (not shown) for suitably treating' the resulting gases.
  • a source of fluids such as a mixture of methanol and air or oxygen
  • il] e prefer to use water as the vaporizable liquid, and to atomize it into the molten b ath by means of a jet of steam at appropriate pressure. Fine atomization of the water is desirable, since otherwise the vaporization may take place with considerable violence.
  • the ⁇ apparatus may be quite compact and relatively inexpensive, since no mechanical agitators are required.
  • the superheated steam arising from the bath may be utilized as desired, but preferably ;for preheating the incoming gases, thereby conserving the heat of reaction.
  • ROBERT 4P COURTNEY. VIRGIL E. MEHARG.
  • finely divided cooling agent is used herein to include liquids, gases, and mixtures thereof.
  • Method of controlling exothermic reactions comprising contacting the wallsI of the reactor with a molt-en saline bath, and agitating said bath and removing excess heat therefrom by means of a finely divided cooling agent, including vwater and steam, contacting directly therewith.
  • a finely divided cooling agent including vwater and steam
  • Method of controlling exothermic reactions comprisingcontacting the walls of the reactor with a molten bath, and agitating said bath and removing excess heat therefrom by contacting directly therewith a finely divided cooling agent including a gaseous component and a liquid which is vaporl izable at the temperature of the bath.
  • vMethod of v controlling exotherlnic reactions comprising contacting the walls of the reactor with a molten bath, and agitating said bath and removing excess heat therefrom by contacting directly therewith a nely divided liquid cooling agent which is vaporizable at the temperature of the bath.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Description

Jan- 5, 1932- R. P. coURTNEY ET AL 1,840,186
METHOD OF CONTROLLING REACTIONS Filed May l2, 1928 Patented Jan. 5, 1932 @NlTED STATES PATENT OFFICE BERT P. COURTNEY, OF EASE.` ORANGE, AND VIRGIL E. MEHARG, F 'BLOOMFIELIL NEW JERSEY, ASSIGNORS TO BAKELITE CORPORATION, OF NEW YORK, N. Y.,
CORPORATION 0F DELAWARE METHOD' OF CONTROLLING REACTIONS Application led May 12,
This invention relates to methods of controlling exothermic reactions of the type requiring a comparatively close heat regulation at temperatures decidedly above that of boiling water. Without thereby limiting our invention we will describe the same by reference, as a specific illustrative example, to the manufacture of formaldehyde by the catalytic oxidation of methanol at a temperature i0 approximating 350 C.
In accordance with our invention the reaction vessel, in tubular or other form, is surrounded by a bath of a molten salt or salts at the appropriate temperature. For eective temperature control it is essential that a certain increment of heat should be removed from the molten saline bath in unit time; and also that the bat-h should. be thoroughly agitated in order to remove the highly heated 26- portions from immediate proximity to the walls of the reactor and to maintain these walls substantially at the temperature of the molten bath. We accomplish both of these objects by injecting directly into the molten bath a spray of a liquid which is readily volatizable at the reacting temperature.
An apparatus embodying the above-mentioned features and suitable for carrying out the method of our invention is illustrated in Bo'the accompanying drawings in which Fig. 1 is a front elevation with the end portions in section on the line 1-1 of Fig. 2,
revealing the internal construction and arrangement of the apparatus;
Fig. 2 is an end view of the apparatus shown in Fig. 1; and
Fig. 3 is a front elevation of the lower end of the saline bath receptacle of Fig. 1 with the front wall of said receptacle broken away.
Referring to the drawings, 1 is the saline bath receptacle, being a -cylindrical tube.
about 6.5 inches internal diameter and inches iong. 'lhe receptacle 1 carries end flanges 2, 2 and is provided with suitable thermometer wells 3, 3, 3, pet cocks 4, 4, 4 for adjusting the height of the saline bath, a vaived saline bath drain 5, and a superheated steam or vapor exit pipe 6. The four spray jets 7, 7, 7, 7 marked Steam injector on Fig. 1 project through the wall of receptacle 1 1928. Serial No. 277,383.
near the lower end thereof, bend toward the inner wall of the receptacle and terminate in nozzles, see Fig. 2. Any desired number of jets may, of course, be used and instead of the jets 7 a ring-shaped, perforated spray pipe 8, see Fig. 3, may be used.
The reaction tubes 9 in the apparatus illustrated are about 0.5 inch in diameter and about 30 inches long and are secured in headers 10, 10. The tubes are filled with the catalyst 11, preferably in the form of spherical balls which assume an orderly arrangement. The group of reaction tubes 9 is positioned within the receptacle 1 with the headers 10, 10 resting against the end flanges 2, 2, preferably with suitable copper- asbestos gaskets 12, 12 therebetween. rEhe endsof the tubes 9 open into chambers 13, 13, formed by the tubular shells 14, 14, having flanges 15, 15 for attachment to flanges 2, 2, that is,vas illustrated flanges 14, 14 are bolted to flanges 2, 2 with the outer edges of headers 10, 10 clamped between them. A perforated plate 17 serves to support the catalyst 11 in the tubes 9. Chambers 13, 13 are provided with projecting conduits 16, 16 for connection to `a source of fluids, such as a mixture of methanol and air or oxygen, to be treated and to apparatus, such as a condenser (not shown) for suitably treating' the resulting gases.
It is to be understood that the invention is not limited to the specific apparatus illustrated and described, it being obvious that the size, shape and construction constitute no part of and may be modified without departure from the invention. n
il] e prefer to use water as the vaporizable liquid, and to atomize it into the molten b ath by means of a jet of steam at appropriate pressure. Fine atomization of the water is desirable, since otherwise the vaporization may take place with considerable violence.
We have found it satisfactory to employ a' molten bath consisting of a mixture of sodium pand potassium nitrates, or nitrites, cooled by water sprayed with about 50% by weight of steam.
The operation as described presents several important advantages, among which the following may be mentioned:
1. The` apparatus may be quite compact and relatively inexpensive, since no mechanical agitators are required.
2. Advantage is talien. of the heat of vaporization of the water or other liquid intro'- duced as such, thereby effecting a marked economy in the use' 0f steam.
3. The direct contact of the steani and water with the molten bath accomplishes the desired heat transfer at high efliciency.
'4. The superheated steam arising from the bath may be utilized as desired, but preferably ;for preheating the incoming gases, thereby conserving the heat of reaction.
It is within the scope of our invention to remove the heat from the molten bathvby a. spray of water or other volatile liquid on the one hand, or by a jet of steam on the other;
In testimo-ny whereof, we aihx our signatures.
ROBERT 4P. COURTNEY. VIRGIL E. MEHARG.
' but neither of these methods is as advantageous as that described above in which a commingled spray of water and steam is employed. rlhe expression finely divided cooling agent is used herein to include liquids, gases, and mixtures thereof.
rihe reaction velocity, and hence the heat evolution, varies considerably throughout the process being comparatively rapid at first and slowing down as the concentration of methanol in the reaction mixture diminishes. Hence we nd it desirable in certain cases to carry out the operation in two or more stages, each in an independently heatcontrolled reaction vessel. and such modification is within the scope of our invention.
We claim:
l. `li/ethod of controlling exothermic reactions, comprising contacting the'walls of the reactor with a molten bath, and agitating said bath and removing excess heat therefrom by means of a finely divided cooling agent,
Y including water and steam, contacting directly therewith.
2. Method of controlling exothermic reactions, comprising contacting the wallsI of the reactor with a molt-en saline bath, and agitating said bath and removing excess heat therefrom by means of a finely divided cooling agent, including vwater and steam, contacting directly therewith.
3. Method of controlling exothermic reactions, comprisingcontacting the walls of the reactor with a molten bath, and agitating said bath and removing excess heat therefrom by contacting directly therewith a finely divided cooling agent including a gaseous component and a liquid which is vaporl izable at the temperature of the bath.
4: vMethod of v controlling exotherlnic reactions, comprising contacting the walls of the reactor with a molten bath, and agitating said bath and removing excess heat therefrom by contacting directly therewith a nely divided liquid cooling agent which is vaporizable at the temperature of the bath.
5. Method of controlling exothermc re-
US277383A 1928-05-12 1928-05-12 Method of controlling reactions Expired - Lifetime US1840186A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2747976A (en) * 1951-05-10 1956-05-29 Oxy Catalyst Inc Surface type catalysis
US2772147A (en) * 1951-04-06 1956-11-27 Oxy Catalyst Inc Exhaust gas treating unit

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2772147A (en) * 1951-04-06 1956-11-27 Oxy Catalyst Inc Exhaust gas treating unit
US2747976A (en) * 1951-05-10 1956-05-29 Oxy Catalyst Inc Surface type catalysis

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