GB832619A - Improvements in or relating to a method of separating phthalic anhydride entrained in gases - Google Patents

Improvements in or relating to a method of separating phthalic anhydride entrained in gases

Info

Publication number
GB832619A
GB832619A GB4481/56A GB448156A GB832619A GB 832619 A GB832619 A GB 832619A GB 4481/56 A GB4481/56 A GB 4481/56A GB 448156 A GB448156 A GB 448156A GB 832619 A GB832619 A GB 832619A
Authority
GB
United Kingdom
Prior art keywords
column
phthalic anhydride
anhydride
hydrocarbon
liquid
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
GB4481/56A
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.)
Compagnie de Saint Gobain SA
Original Assignee
Compagnie de Saint Gobain SA
Manufactures des Glaces et Produits Chimiques de Saint Gobain SA
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 Compagnie de Saint Gobain SA, Manufactures des Glaces et Produits Chimiques de Saint Gobain SA filed Critical Compagnie de Saint Gobain SA
Publication of GB832619A publication Critical patent/GB832619A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/54Preparation of carboxylic acid anhydrides
    • C07C51/573Separation; Purification; Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0832619/III/1> Gases containing entrained phthalic anhydride, such as the hot gases obtained from the synthesis of phthalic anhydride by catalytic oxidation, are washed with a liquid aliphatic hydrocarbon or a mixture of liquid aliphatic hydrocarbons having a boiling-point higher than 200 DEG C., whereby the anhydride passes from the gas into the liquid hydrocarbon to form a solution; this solution is distilled using a fractionating column and a vapour mixture comprising the anhydride and hydrocarbon leaves the head of the column; the vapour is condensed and the condensate is cooled to a temperature at which it separates into two phases-one of which is rich in anhydride. A petroleum fraction boiling between 260 DEG and 265 DEG C. may be used as washliquid. Penta- or tetradecane may also be used. The distillation is preferably carried out under reduced pressure. The anhydride-rich phase of the condensate may be separated in either the liquid state or the solid state. A gas, at a temperature of 140 DEG C., containing 50 grams of finely-divided phthalic anhydride per cubic meter is passed through pipe 1 into the lower part of plate-type column A; and a mixture of straight-chain hydrocarbons, boiling between 260 and 265 DEG C., is introduced into the top of the column through pipe 3. The temperature in column A is maintained at 140 DEG C. The gases leaving the column through pipe 2 are practically free from phthalic anhydride; these gases are cooled to recover any hydrocarbon carried over. The solution leaving column A through pipe 4 contains 9% phthalic anhydride; and this solution is distilled in column C, the base of which is maintained at a temperature of 180 DEG C. while the head of the column is maintained under an absolute pressure of 60 mm. Hg. The vapour from the head of the column contains 25% phthalic anhydride, and is condensed in condenser C1, which is maintained at 130 DEG C. The condensate flows into decanter D, which is also maintained at 130 DEG C., where it separates into two liquid layers. The lower layer, which comprises phthalic anhydride containing a small amount of dissolved hydrocarbon, is withdrawn from decanter D and is stripped in plate-type column E, which is heated to 180 DEG C and is maintained at an absolute pressure of 50 mm. Hg. Substantially pure phthalic anhydride is withdrawn from the base of column E. The hydrocarbon vapour leaving the head of column E is condensed in condenser C2; and the condensate is returned to the decanter. The hydrocarbon layer from decanter D is returned to column C as reflux. Any naphthoquinones, present in the initial gas, accumulate together with hydrocarbons in the base of column C. The naphthoquinones are separated from the hydrocarbons in refrigerator F; and the hydrocarbons are then pumped back to the top of column A after being re-heated to 140 DEG C.ALSO:Gases containing entrained phthalic anhydride, such as the hot gases obtained from the synthesis of phthalic anhydride by catalytic oxidation, are washed with a liquid aliphatic hydrocarbon or a mixture of liquid aliphatic hydrocarbons having a boiling point higher than 200 DEG C., whereby the anhydride passes from the gas into the liquid hydrocarbon to form a solution; this solution is distilled using a fractionating column and a vapour mixture comprising anhydride and hydrocarbon leaves the head of the column; the vapour is condensed and the condensate is cooled to a temperature at which it separates into two phases, one of which is rich in phthalic anhydride. A petroleum fraction boiling between 260 DEG and 265 DEG C. may be used as wash-liquid, Pentaor tetra-decane may also be used. The distillation is preferably carried out under reduced pressure. The anhydride-rich phase of the condensate may be separated in either the liquid state or the solid state. Suitable apparatus for carrying out the method of the invention is described (see Group III).
GB4481/56A 1955-02-11 1956-02-13 Improvements in or relating to a method of separating phthalic anhydride entrained in gases Expired GB832619A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR832619X 1955-02-11

Publications (1)

Publication Number Publication Date
GB832619A true GB832619A (en) 1960-04-13

Family

ID=9296112

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4481/56A Expired GB832619A (en) 1955-02-11 1956-02-13 Improvements in or relating to a method of separating phthalic anhydride entrained in gases

Country Status (1)

Country Link
GB (1) GB832619A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4568427A (en) * 1982-02-27 1986-02-04 Basf Aktiengesellschaft Continuous isolation of phthalic anhydride and maleic anhydride from reaction gases
WO1998023572A1 (en) * 1996-11-29 1998-06-04 Exxon Chemical Patents Inc. Solvent assisted process for recovery of phthalic anhydride in the liquid phase by distillation
CN111486662A (en) * 2020-03-31 2020-08-04 北京三泰天洁气体净化技术有限公司 Method and device for low-temperature separation of synthesis gas and preparation of ammonia synthesis gas

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4568427A (en) * 1982-02-27 1986-02-04 Basf Aktiengesellschaft Continuous isolation of phthalic anhydride and maleic anhydride from reaction gases
WO1998023572A1 (en) * 1996-11-29 1998-06-04 Exxon Chemical Patents Inc. Solvent assisted process for recovery of phthalic anhydride in the liquid phase by distillation
CN111486662A (en) * 2020-03-31 2020-08-04 北京三泰天洁气体净化技术有限公司 Method and device for low-temperature separation of synthesis gas and preparation of ammonia synthesis gas

Similar Documents

Publication Publication Date Title
US2551593A (en) Extractive distillation of alcohols from close-boiling aqueous mixtures
US3745092A (en) Recovery and purification of ethylene oxide by distillation and absorption
US1963809A (en) Process of obtaining constituents of air having a higher boiling point than oxygen
GB943817A (en) Improvements relating to processes for obtaining pure methanol from crude synthetic methanol
US2236964A (en) Separation of acetylene from mixtures
GB833230A (en) An improved method of recovering the anhydrides of organic diacids from gases
US2679472A (en) Separation of hydrocarbons by azeotropic distillation
US2250949A (en) Process for the separation of hydrocarbons from gases containing them
JPS60104026A (en) Distillation post-treatment of 6-20 c atom higher alcohol containing water and methanol
KR980000524A (en) Preparation of a mixture of dimethyl ether and chloromethane and fractionation method using water as extractant
US4508928A (en) Ethanol extraction process
GB832619A (en) Improvements in or relating to a method of separating phthalic anhydride entrained in gases
US1866800A (en) Process of increasing the concentration of olefines in a mixture containing same
US2356986A (en) Process for separating hydrocarbons
US2327134A (en) Extraction of hydrocarbons from gas mixtures which, besides hydrocarbons, contain carbon dioxide
US3745093A (en) Process for separating hexafluoroacetone from hydrogen fluoride
US2264878A (en) Separation of gaseous mixtures
US2379696A (en) Recovery of olefinic hydrocarbons
US1877291A (en) Continuous method of producing esters from olefins
US3390534A (en) Method for separation of multicomponent mixtures
US2974174A (en) Solvent extraction process
US2467197A (en) Azeotropic distillation of styrene
US1360853A (en) Apparatus and method for separating the constituents of air or other gaseous mixtures
GB901079A (en) Purifying furfural
US2299283A (en) Treatment of enriched benzol wash oil or the like