DE436522C - Process for the production of phenols from ammonia water or technical wastewater - Google Patents

Process for the production of phenols from ammonia water or technical wastewater

Info

Publication number
DE436522C
DE436522C DEZ15146D DEZ0015146D DE436522C DE 436522 C DE436522 C DE 436522C DE Z15146 D DEZ15146 D DE Z15146D DE Z0015146 D DEZ0015146 D DE Z0015146D DE 436522 C DE436522 C DE 436522C
Authority
DE
Germany
Prior art keywords
phenols
ammonia water
bases
benzene
production
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
DEZ15146D
Other languages
German (de)
Inventor
Dr Fritz Ulrich
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.)
ZECHE MATHIAS STINNES
Original Assignee
ZECHE MATHIAS STINNES
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 ZECHE MATHIAS STINNES filed Critical ZECHE MATHIAS STINNES
Priority to DEZ15146D priority Critical patent/DE436522C/en
Application granted granted Critical
Publication of DE436522C publication Critical patent/DE436522C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/005Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by obtaining phenols from products, waste products or side-products of processes, not directed to the production of phenols, by conversion or working-up
    • C07C37/009Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by obtaining phenols from products, waste products or side-products of processes, not directed to the production of phenols, by conversion or working-up from waste water

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Gewinnung von Phenolen aus Ammoniakwasser oder technischen Abwässern. Nach den bis jetzt bekannt gewordenen Verfahren geschieht die Waschung bzw. Entphenolierung des Ammoniakwassers ausschließlich durch Benzol oder dessen Homologen. Dieses Verfahren hat den großen Nachteil, daß es nicht ermöglicht, die Phenole des Ammoniakwassers, und zwar insbesondere die wasserlösliche wertvolle Carbolsäure restlos zu erfassen. Mehrere auf Grund dieses Verfahrens angestellte Versuche haben ergeben, daß im Mittel nur rund 65 Prozent der in dem Ammoniakwasser vorhandenen Pheno-le noch auf wirtschaftliche Weise gewonnen werden können, während auf die restlichen, vornehmlich aus Carbolsäure bestehenden 35 Prozent verzichtet werden muß.Process for the extraction of phenols from ammonia water or technical Sewage. Washing is carried out according to the processes that have become known up to now or dephenolation of the ammonia water exclusively with benzene or its Homologues. This method has the major disadvantage that it does not allow the Phenols of ammonia water, especially the valuable ones which are water-soluble Carbolic acid to be recorded completely. Several employees on the basis of this procedure Tests have shown that on average only around 65 percent of that in the ammonia water existing phenols can still be obtained economically while the remaining 35 percent, which consists primarily of carbolic acid, is dispensed with must become.

Gemäß der Erfindung wird der vorgenannte Nachteil dadurch vermieden, daß man den bisher verwendeten Extraktionsmitteln Basen des Kokerei- oder Urteers, beispielsweise Pyridine, Chinoline oder deren Homologen, zusetzt, deren Siedepunkt zweckmäßig so hoch liegt, daß die Wasserlöslichkeit dieser Körperklasse nicht mehr in Erscheinung tritt. Die höhere Waschwirkung, die man mit einem derartigen basischen Waschöl erreicht, läßt sich leicht durch die chemische Affinität der Basen zu den sauren Phenolen erklären. Demgemäß ist die eigentliche Waschwirkung bei diesem Verfahren den Basen selbst zuzuschreiben, während Benzol oder dessen Homologen als Lösungs- oder Verdünnungsmittel für diese Stoffe anzusehen sind und daher auch durch Benzin oder andere Neutralöle ersetzt werden können.According to the invention, the aforementioned disadvantage is avoided by that the extraction agents used so far are bases of coke oven tar or primeval tar, for example pyridines, quinolines or their homologues, add their boiling point is expediently so high that the water solubility of this body class is no longer appears. The higher detergency you get with such a basic one Reached washing oil, can be easily achieved by the chemical affinity of the bases to the explain acidic phenols. Accordingly, the actual detergency in this process is to be ascribed to the bases themselves, while benzene or its homologues are or diluents for these substances are to be considered and therefore also by gasoline or other neutral oils can be replaced.

Vergleichende Versuche, die nach den bisher üblichen und dem den Gegenstand der , Erfindung bildenden Verfahren angestellt wurden, haben folgende Ergebnisse geliefert: Beispiel z.Comparative experiments based on the previously customary and the subject of the process forming the invention have the following results delivered: Example e.g.

a. 2 1 Ammoniakwasser mit einem Phenolgehalt von 4,79 im Liter werden einmal mit 4o Prozent (8oo ccm) gogrädigem Benzol bei ro° C gewaschen. Die Phenolausbeute beträgt 53 Prozent.a. 2 1 ammonia water with a phenol content of 4.79 per liter Washed once with 40 percent (8oo ccm) deg benzene at ro ° C. The phenol yield is 53 percent.

b. Desgleichen werden 21 einmal mit 8oo ccm eines Waschmittels behandelt, welches aus gogräd@gem Benzol und ro Prozent Basen (Siedepunkt Zoo bis 25o°) besteht. Die Ausbeute an Phenol beträgt hierbei 82 Prozent. Der Mehrertrag an Phenol gegenüber Versuch a ist somit rund 5o Prozent. Verluste an Basen konnten nicht festgestellt erden.b. Likewise, 21 are treated once with 8oo ccm of a detergent, which consists of gogräd @ gem benzene and ro percent bases (boiling point zoo up to 25o °). The phenol yield is 82 percent. The higher yield of phenol compared to Trial a is thus around 50 percent. Loss of bases could not be determined earth.

Beispiel e.Example e.

2 1 desselben Ammoniakwassers werden zweimal mit einer 2oprozentigen Menge (also 2 X 400 ccm) Waschöl, bestehend aus gggrädigem Benzol mit 2o Prozent von 23o° an siedenden Basen gewaschen. Dem so behandelten Wasser lassen sich durch nachfolgende Extraktion mit Äther keine nachweisbaren Mengen von Phenolen mehr entziehen. Die Ausbeute ist daher als nahezu quantitativ anzusprechen.2 1 of the same ammonia water are used twice with a 2% Amount (i.e. 2 X 400 ccm) of washing oil, consisting of gggrädigem benzene with 2o percent washed at 230 ° on boiling bases. The water treated in this way can pass through subsequent Extraction with ether no detectable amounts of Eliminate more phenols. The yield can therefore be addressed as almost quantitative.

Bei derselben Versuchsätiordnung könnte mit gogrädigem Benzol als Waschmittel allein nur eine Ausbeute von rund 65 Prozent erhalten werden.With the same test order, benzene could be used as a Detergent alone only yields around 65 percent.

Beispiel 3. Example 3.

500 ccm eines Ammoniakrohwassers mit 3J99 Phenol im Liter werden dreimal mit Zoo ccm eines entphenolierten Teeröls (Siedepunkt Zoo bis 25o0), in dem an und für sich ¢ Prozent Basen enthalten sind, die hier frei zur Wirkung gelangen, gewaschen. Es konnten so 82 Prozent der Phenole gewonnen werden. 500 ccm of raw ammonia water with 3J99 phenol per liter are washed three times with zoo ccm of a dephenolated tar oil (boiling point zoo up to 25o0), which in and of itself contains ¢ percent bases, which are freely effective here. In this way, 82 percent of the phenols could be obtained.

Beispiel ¢.Example ¢.

5oo ccm eines Ammoniakwassers, das wie vorher 3,i9 9 Phenole im Liter enthält, wird dreimal mit je ioo ccm Basen, die aus Teeröl gewonnen wurden (Siedepunkt 24o bis 32o°), gewaschen. Rund 75 Prozent der Phenole konnten extrahiert werden.5oo cc of an ammonia water, which as before 3 containing i9 9 phenols per liter is (boiling point of 24o to 32o °) washed three times with ioo cc bases obtained from tar oil. Around 75 percent of the phenols could be extracted.

Claims (3)

PATENT-ANspRÜcfIE: i. Verfahren zur Gewinnung von Phenolen aus Ammoniakwasser oder technischen Abwässern, dadurch gekennzeichnet, daß man die phenolhaltigen Wässer mit einem Gemisch aus Benzol oder dessen Homologen und Basen des Kokerei- oder Urteers behandelt. PATENT CLAIM: i. Process for the production of phenols from ammonia water or industrial wastewater, characterized in that the phenol-containing waters with a mixture of benzene or its homologues and bases of coke oven tar or primordial tar treated. 2. Verfahren nach Anspruch i, dadurch gekennzeichnet, daß man an Stelle des Benzol-Basen-Gemisches entphenolierte Teeröle, die ihrem Ursprung gemäß noch Basen enthalten, verwendet. 2. The method according to claim i, characterized in that one in place of the benzene-base mixture dephenolated tar oils, which according to their origin still Bases included, used. 3. Verfahren nach Anspruch i, dadurch gekennzeichnet, daß man an Stelle des Gemisches von Benzol und Basen nur die Basen verwendet.3. The method according to claim i, characterized in that that only the bases are used instead of the mixture of benzene and bases.
DEZ15146D 1925-03-14 1925-03-14 Process for the production of phenols from ammonia water or technical wastewater Expired DE436522C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEZ15146D DE436522C (en) 1925-03-14 1925-03-14 Process for the production of phenols from ammonia water or technical wastewater

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEZ15146D DE436522C (en) 1925-03-14 1925-03-14 Process for the production of phenols from ammonia water or technical wastewater

Publications (1)

Publication Number Publication Date
DE436522C true DE436522C (en) 1926-11-03

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
DEZ15146D Expired DE436522C (en) 1925-03-14 1925-03-14 Process for the production of phenols from ammonia water or technical wastewater

Country Status (1)

Country Link
DE (1) DE436522C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE760862C (en) * 1940-08-21 1953-05-11 Ig Farbenindustrie Ag Process for the separation of phenols from phenol-containing waters
DE1259343B (en) * 1962-03-28 1968-01-25 Kao Corp Process for the extraction of phenol from water containing phenol
DE3209929A1 (en) * 1981-03-19 1982-11-11 Koei Chemical Co., Ltd., Osaka METHOD FOR TREATING PHENOLIC AQUEOUS SOLUTIONS

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE760862C (en) * 1940-08-21 1953-05-11 Ig Farbenindustrie Ag Process for the separation of phenols from phenol-containing waters
DE1259343B (en) * 1962-03-28 1968-01-25 Kao Corp Process for the extraction of phenol from water containing phenol
DE3209929A1 (en) * 1981-03-19 1982-11-11 Koei Chemical Co., Ltd., Osaka METHOD FOR TREATING PHENOLIC AQUEOUS SOLUTIONS

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