US1698798A - Rectification of acetic acid - Google Patents

Rectification of acetic acid Download PDF

Info

Publication number
US1698798A
US1698798A US49821A US4982125A US1698798A US 1698798 A US1698798 A US 1698798A US 49821 A US49821 A US 49821A US 4982125 A US4982125 A US 4982125A US 1698798 A US1698798 A US 1698798A
Authority
US
United States
Prior art keywords
acetic acid
column
acid
rectification
crude
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
Application number
US49821A
Inventor
Legendre Georges Felix
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.)
BARBET ETS
FIRM Ets BARBET Ste
Original Assignee
BARBET ETS
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 BARBET ETS filed Critical BARBET ETS
Application granted granted Critical
Publication of US1698798A publication Critical patent/US1698798A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation

Definitions

  • the apparatus which is described hereinafter is provided for the purpose of obtaining a continuity in the rectification of acetic acid, commencing with crude acids, having already a certain amount of concentration.
  • A is the vat of crude acid to be rectified
  • B the ioat regulator for the supply
  • C vthe supply tap.
  • the liquid is pre-heated in a spiral tube D placed in'the head of the rst plate column G.
  • H is the cooling condenser.
  • test device J The water containing traces of acetic acid condensed in H is led away through the test device J, some of which is utilized 'for the reflux being reheated upon the chimney plate D from whence it descends' through the column G. With regard to 'the pre-heated crude acid, this enters at thetop of the tubular.
  • heater E which is a stream action tubular heater.
  • the degree of concentration at which the water containing a small quantity of acetic acid issues at J depends essentially upon the number of plates, that is to say the more or less perfect working ⁇ of the column Gr.
  • the amount of steam used proportions itself naturally to the volume of the crude acid, as required, since an extraction of water proportionate to the dilution of the crude acid has to be made; 1
  • the said water is pre-heated in the spiral N, and then passes through the pipe 5 6 to the stream action heater O, which is similar to -the heater E.
  • the water is entirely 105 vaporized into steam and entersthe column l M about half way up.
  • the bject is to make the water as poorl as possible in acetic acid pass out at the top;
  • P is the cooling 'condenser,'Q the testing device of the 110 Water condensate which is very poor in acetic acid.
  • the siphon pipe 9-10 leads the concentrated acetic acid into the heating caldron R Which provides all lthe necessary heat to the column M.
  • the rectifier G would become a finishing column. It would be supplied exclusively by the vapours from the heater S.
  • Apparatus for the continuous rectication of crude' acetic acid comprising a rst rectification column adapted to be continuouslyfed With crude acetic acid, means for preheating the crude acetic acid, and means for vapourizing the preheated acid fed to the said column, a condenser communicating with the top of said column to condense Water containing a small quantity of acetic acid evolved from said column, a
  • a vapourizer for the rectified dehydrated acid communicating With the bottom of said column, a condenser communicating With said vapourizer, a liquid separator interposed between said condenser and vapourizer, and a receiver for the pure dehydrated acetic acid from said condenser.
  • Apparatus for the continuous rectification of crude acetic acid comprising a first rectification column adapted to be continuously fed with crude acetic acid, means for pre1 heating the crude acetic acid, and means for vapourizing the preheated acid fed to the said column a condenser communicating With the top of said column to condense vvater'containing a small quantity of acetic acid evolved from said column, a pipe from said condenser to convey condensate to said column to provide reflux therefor, a vapourizer for the rectified dehydrated acid communicating with theqbottom of said column, a condenser communicating With said vapourizer, a liquid separator interposed between said condenser and vapourizer, a receiver for the pure dehydrated acetic acid from lsaid condenser, a second rectification column communicating With and adapted to receive Weak acetic acid evolved from the first rectification column, means for preheating and means for vapourizing the said Weak-acid supplied to' said second column
  • vapourizers for the preheatedacid supplied to the columns constitute regulators for regulating'the heating of the acid in proportion to the degree of hydration thereof.

Landscapes

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

Description

Jah. 15, 1929.
G. F.l LEGENDRE Filed Aug. 12, 1925 foral/MAP nl .rz /d//n Y Alvi/FIM nl!! HMH M im wir.
PaaateaJaa. 15, 1929i.
M l Y 1,698,798 .PATENT .ori-frcs.'
GEORGES FELIX LEGENDRE, 0F vPARIS, FRANCE, ASSIG'NOR TO THE FIRM SOCIT DES ETABLISSEMENTS BARBET, F PARIS, FRANCE.
REGTIFICATION or .sonrie ACID.
Application med .august 1a, 1925, serial 1ra-19,821, and in France August-14, 199A.
In Whatever way acetic acid is prepared industrially, by mycoderma aceti, by the carbonization of Wood or by synthesis, this crude acid is impure and aqueous and it is 5 purified by rectification. K
This rectification has this particularA feature, that the acetic acid, boiling at about 117 is a tail product relativel to the water, and that consequently the re ing effect of the plates is'exerted upon the water to be eliminated with the sole purpose of ensuring thatlthis Water will take away with it as little acid as possible. It is therefore of importance to make this operation as economical as possible in. steam, and it is only by making it continuous that this can be attained. Moreover in a rectifier charged periodically there isine'vitably obtained a gradually increasing concentration iny acetic acid of the head liquors until a moment arrives when anhydrous acid is obtained, and all these products have then to be passed once more through the rectifier, in
,order to avoid losses in acetic acid.
There is another advantage 1n favour vof continuity, which is that the apparatus made of copper which is usually employedV is only violently attacked by -acetic acid in Ythe 'presence of air. Once the continuous operation is started there is no more air in the apparatus so that the action of the acidis` avoided, while for the discontinuous operation, for each stopthat is to say each day, .-an entry of air takes place during the emptying and recharging period.
The apparatus which is described hereinafter is provided for the purpose of obtaining a continuity in the rectification of acetic acid, commencing with crude acids, having already a certain amount of concentration.
A is the vat of crude acid to be rectified, B the ioat regulator for the supply, C vthe supply tap. -The liquid is pre-heated in a spiral tube D placed in'the head of the rst plate column G. H is the cooling condenser.
The water containing traces of acetic acid condensed in H is led away through the test device J, some of which is utilized 'for the reflux being reheated upon the chimney plate D from whence it descends' through the column G. With regard to 'the pre-heated crude acid, this enters at thetop of the tubular. heater E which is a stream action tubular heater.
exactly in the same proportions as this supply. It provides therefore ofitself'an excellent regulation of the rectification.
The degree of concentration at which the water containing a small quantity of acetic acid issues at J depends essentially upon the number of plates, that is to say the more or less perfect working` of the column Gr. For a same hourly weight of crude acetic acid to be dehydrated to` glacial acetic acid, the amount of steam used, as is appropriate, proportions itself naturally to the volume of the crude acid, as required, since an extraction of water proportionate to the dilution of the crude acid has to be made; 1
At the base of the dehydration column G a very concentrated or even completely dehydrated crude acid is obtained. It passes gradually through the siphon pipe 1 2 into the caldron K, This caldronprovides at the same time the acid vapour necessary'for the rectifier G, and through the tube 3 4, the pure acid which is cooled in the silver spiral tube L, passing but through the test ing device l.
It is advantageous to provide, before the inlet into the spiral, a vessel 4 for separating out the drops carried along mechanically, for Athey are contaminated with copper.
The water containing a small quantit of acetic acid which issues from the test sa e J, supplies the left hand column M, which is 10o a -recuperating column. For this purpose, the said water is pre-heated in the spiral N, and then passes through the pipe 5 6 to the stream action heater O, which is similar to -the heater E. The water is entirely 105 vaporized into steam and entersthe column l M about half way up. Here the bject is to make the water as poorl as possible in acetic acid pass out at the top; P is the cooling 'condenser,'Q the testing device of the 110 Water condensate which is very poor in acetic acid.
The excess of Water containing a small quantity of acetic acid, returning along pipe 7 8, is reheated upon. the chimney plate N and forms the reflux of the rectifying plates.
At the baseof the column M, the siphon pipe 9-10 leads the concentrated acetic acid into the heating caldron R Which provides all lthe necessary heat to the column M.
Herefalso must be provided an outletof concentrated acid which Will have to return, through the pipe 13-14 to the first rectifier G. In order to be able to regulate more easily the magnitude of this extraction, which is essential, a second heater S which is tubular is provided as shown in the drawing. It is supplied through the pipe 11-l2, and at 12 is provided a regulating cock. Once the liquid has entered S, it is completely vaporized and this vapour thus passes naturally into the column G. It will be arranged for this acid vapour to be of about the same acetic concentration as the crude supply liquid.J
If the crude liquids are to be dealt with which are veryv poor in acetic acid, such as pyroligneous liquids from wood carbonization Works (approximately 8% of acid), or else vinegar obtained by means of mycoderma aceti, these poor liquids would be supplied into the column M and no longer into G.
. The operation Would be carried out in M in such a Way as to obtain Water containing as little acid as possible at the outlet from P any vapours of acetic acid which might be carried over being bubbled through Water containingA carbonate of soda in solution, or else milkof lime, or any alkali.
The rectifier G would become a finishing column. It would be supplied exclusively by the vapours from the heater S.
' What vI claim:
l. Apparatus for the continuous rectication of crude' acetic acid comprising a rst rectification column adapted to be continuouslyfed With crude acetic acid, means for preheating the crude acetic acid, and means for vapourizing the preheated acid fed to the said column, a condenser communicating with the top of said column to condense Water containing a small quantity of acetic acid evolved from said column, a
pipe from said condenser to c onvey condensate to said column to provide reiiux therefor, a vapourizer for the rectified dehydrated acid communicating With the bottom of said column, a condenser communicating With said vapourizer, a liquid separator interposed between said condenser and vapourizer, and a receiver for the pure dehydrated acetic acid from said condenser.
2. Apparatus for the continuous rectification of crude acetic acid comprising a first rectification column adapted to be continuously fed with crude acetic acid, means for pre1 heating the crude acetic acid, and means for vapourizing the preheated acid fed to the said column a condenser communicating With the top of said column to condense vvater'containing a small quantity of acetic acid evolved from said column, a pipe from said condenser to convey condensate to said column to provide reflux therefor, a vapourizer for the rectified dehydrated acid communicating with theqbottom of said column, a condenser communicating With said vapourizer, a liquid separator interposed between said condenser and vapourizer, a receiver for the pure dehydrated acetic acid from lsaid condenser, a second rectification column communicating With and adapted to receive Weak acetic acid evolved from the first rectification column, means for preheating and means for vapourizing the said Weak-acid supplied to' said second column, a condenser communicating With the top of said second column, a pipe from said condenser'to convey condensate to said second column to provide reflux therefor, a vapourizer communicating with the bpttom of said second column to supply hot vapours thereto, a second vapourizer communicating with the bottom of said column to vapourlze the concentratedV acetic acid therefrom and a pipe for conveying said concentrated acid vapours from said vapourizer to the first mentioned rectication column.
3. Apparatus as claimed in claim 2 in which the vapourizers for the preheatedacid supplied to the columns constitute regulators for regulating'the heating of the acid in proportion to the degree of hydration thereof.
In testimony whereof I have signed my name to this specification.
GEORGES FELIX LEGENDRE.
US49821A 1924-08-14 1925-08-12 Rectification of acetic acid Expired - Lifetime US1698798A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR1698798X 1924-08-14

Publications (1)

Publication Number Publication Date
US1698798A true US1698798A (en) 1929-01-15

Family

ID=9680295

Family Applications (1)

Application Number Title Priority Date Filing Date
US49821A Expired - Lifetime US1698798A (en) 1924-08-14 1925-08-12 Rectification of acetic acid

Country Status (1)

Country Link
US (1) US1698798A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450611A (en) * 1945-02-10 1948-10-05 Armour & Co Distillation apparatus for treating fatty acid containing stock
US3002896A (en) * 1958-03-20 1961-10-03 Heinz Co H J Process for continuous concentration of vinegar
US5662780A (en) * 1995-09-29 1997-09-02 Showa Denko K.K. Process for purifying acetic acid

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2450611A (en) * 1945-02-10 1948-10-05 Armour & Co Distillation apparatus for treating fatty acid containing stock
US3002896A (en) * 1958-03-20 1961-10-03 Heinz Co H J Process for continuous concentration of vinegar
US5662780A (en) * 1995-09-29 1997-09-02 Showa Denko K.K. Process for purifying acetic acid

Similar Documents

Publication Publication Date Title
US1469447A (en) Absolute alcohol
US1698798A (en) Rectification of acetic acid
US2162838A (en) Process for purification of gases
GB795545A (en) Concentration of hydrazine solution by evaporation and rectification
US2164275A (en) Distillation of glycerin
US939980A (en) Process of making acetates.
US2650249A (en) Process for treating methyl acetate
RU2366711C2 (en) Method for producing of rectified ethanol "alpha"
US3065085A (en) Juice concentration system
US1303321A (en) Edward j
US1454462A (en) Process of producing high-grade esters
US1614877A (en) Process for the distillation of alcohol
US2922751A (en) Debenzolizing wash oil
CN214881194U (en) Methanol rectification extraction water transformation system
US2663681A (en) Recovery of lower acid anhydrides by distillation
RU65779U1 (en) SYSTEM OF SUPPLY OF HEAT FLOWS WHEN RECEIVING A RECTIFIED ALCOHOL IN A BRAKE RECTIFICATION INSTALLATION (OPTIONS)
SU390139A1 (en) DEVICE OF CONTINUOUS ACTION FOR OBTAINING COGAR ALCOHOL
US1568349A (en) Process of obtaining absolute propyl alcohol
CN208541823U (en) A kind of varying duty system for benzene distillation device
US436684A (en) Emile augustin barret
SU438685A1 (en) The method of separation of food ethyl alcohol from the ether-aldehyde fraction
US1945177A (en) Continuous process for producing esters
RU1806181C (en) Rectification plant for extraction of ethyl alcohol from ethanol head fraction
SU133846A1 (en) The method of obtaining horse alcohol
SU676609A1 (en) Brandy producing method