DE138392C - - Google Patents

Info

Publication number
DE138392C
DE138392C DENDAT138392D DE138392DA DE138392C DE 138392 C DE138392 C DE 138392C DE NDAT138392 D DENDAT138392 D DE NDAT138392D DE 138392D A DE138392D A DE 138392DA DE 138392 C DE138392 C DE 138392C
Authority
DE
Germany
Prior art keywords
phosphorus
chlorine
carbon
metaphosphate
coal
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.)
Active
Application number
DENDAT138392D
Other languages
German (de)
Publication of DE138392C publication Critical patent/DE138392C/de
Active legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/10Halides or oxyhalides of phosphorus

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

KAISERLICHESIMPERIAL

PATENTAMT.PATENT OFFICE.

PatentschriftPatent specification

KLASSE 12«. -J CLASS 12 «. -J

Patentirt im Deutschen Reiche vom 16. August 1901 ab.Patented in the German Empire on August 16, 1901.

J. Riban (Compt. rend. 95, S. 1161 ff.) hat gefunden, dafs man aus Tricalciumphosphat durch Mischen mit Kohle und Ueberleiten von Chlor und Kohlenoxyd in der Wärme Phosphoroxychlorid darstellen kann. Aus der Thatsache, dafs weder durch Kohle noch durch Kohlenoxyd, jedes für sich allein als Reductionsmittel angewendet, beim Behandeln mit Chlor aus TricalciumphosphatPhosphoroxychlorid erhalten wird, sondern nur Phosphor, Phosphortrichlorid oder Phosphorpentachlorid je nach Stärke des Chlorstroms, schliefst Riban, dafs ein Zusammenwirken der Kohle und des Kohlenoxyds in der Weise stattfindet, dafs die erstere als Ueberträger der reducirenden Wirkung des letzteren dient. Er giebt dieser Meinung auch durch die von ihm aufgestellten Formeln Ausdruck, in denen nur das Kohlenoxyd als Reductionsmittel erscheint:J. Riban (Compt. Rend. 95, pp. 1161 ff.) found that tricalcium phosphate can be obtained by mixing with charcoal and passing over Chlorine and carbon monoxide can represent phosphorus oxychloride in the heat. From the fact that neither by coal nor by carbon monoxide, each of them alone as a reducing agent applied, obtained when treating with chlorine from tricalcium phosphate phosphorus oxychloride but only phosphorus, phosphorus trichloride or phosphorus pentachloride depending on the strength of the Stream of chlorine, Riban concludes that there is a co-operation of coal and carbon dioxide takes place in such a way that the former as a carrier of the reducing effect of the the latter serves. He also expresses this opinion through the formulas he has drawn up, in which only the carbon dioxide appears as a reducing agent:

ι. P2 O5 (Ca O)3 + 2 C O + 4 Cl =ι. P 2 O 5 (Ca O) 3 + 2 CO + 4 Cl =

P2OsCaO + 2 COs + 2Ca ch-P 2 OsCaO + 2 COs + 2Ca c h-

2. P2O5CaO + 4 C O + 8 C/ = 2. P 2 O 5 CaO + 4 C O + 8 C / =

2 PO Cl3 -f- Ca CL2 + 4 C O2. 2 PO Cl 3 -f- Ca CL 2 + 4 CO 2 .

Demgegenüber wurde nun gefunden, dafs man in der Phase, die durch die zweite Formel ausgedrückt wird, das Kohlenoxyd durch Kohle ersetzen kann, dafs man also durch Kohle allein Phosphoroxychlorid erhalten kann, sobald man von einem Metaphosphat direct ausgeht. On the other hand, it has now been found that in the phase represented by the second formula is expressed that carbon oxide can be replaced by charcoal, that is to say by charcoal only phosphorus oxychloride can be obtained as soon as one starts directly from a metaphosphate.

Man bereitet sich z. B. in der bei der Darstellung von Phosphor üblichen Weise (Behandeln von Tricalciumphosphat mit Schwefelsäure, Versetzen der vom Gips abgesaugten Lösung des primären Calciumphosphats mit Kohle, Eindampfen und schwaches Glühen) eine Kohle enthaltende Schmelze von Calciummetaphosphat. Dieselbe wird zerkleinert und in einem geeigneten Apparat, welcher mit Kühler und Vorlage versehen ist, schwach geglüht. Gleichzeitig wird ein Strom trockenen Chlors eingeleitet. Alsbald sammelt sich in der Vorlage ein Flüssigkeit an, welche nach nochmaligem Destilliren reines Phosphoroxychlorid darstellt.One prepares z. B. in the usual way in the representation of phosphorus (treat of tricalcium phosphate with sulfuric acid, addition of the primary calcium phosphate solution extracted from the gypsum Coal, evaporation and faint glow) a coal-containing melt of calcium metaphosphate. The same is crushed and lightly calcined in a suitable apparatus which is provided with a cooler and receiver. At the same time a stream of dry chlorine is introduced. Immediately collects in the Submission of a liquid which, after further distillation, is pure phosphorus oxychloride represents.

Die technischen Vortheile vorliegender Erfindung bestehen darin, dafs einmal die Apparatur eine einfachere sein kann, indem nur ein Gas eingeführt zu werden braucht. Durch das Fortfallen des brennbaren und giftigen Kohlenoxyds wird auch eine gröfsere Betriebssicherheit herbeigeführt. Ferner tritt eine bedeutende Ersparnifs an Chlor ein, indem gegenüber dem Triphosphat zwei Drittel Calcium weniger in Chlorcalcium überzuführen sind. Die zu erhitzenden, die Kohlephosphatmischung enthaltenden Gefäfse können relativ kleiner sein bezw. gestatten eine bessere Ausnutzung, weil das Metaphosphat mehr Phosphor enthält wie das Triphosphat.The technical advantages of the present invention consist in the fact that, on the one hand, the apparatus a simpler one, in that only one gas needs to be introduced. By the Elimination of the flammable and poisonous carbon monoxide also increases operational safety brought about. Furthermore, there is a considerable saving in chlorine, in that compared with the Triphosphate two thirds of calcium less need to be converted into calcium chloride. The ones to be heated the vessels containing the carbon phosphate mixture can be relatively smaller or. allow better utilization because the metaphosphate contains more phosphorus than the triphosphate.

Claims (1)

Patent-Anspruch:
Verfahren zur Darstellung von Phosphoroxychlorid durch Ueberleiten von Chlor über ein erhitztes Gemisch von Kohle mit einem Metaphosphat.
Patent claim:
Process for the preparation of phosphorus oxychloride by passing chlorine over a heated mixture of carbon with a metaphosphate.
BERLIN. GEDRUCKT IN DER KEICHSDRUCKEREt.BERLIN. PRINTED IN THE KEICHSDRUCKEREt.
DENDAT138392D Active DE138392C (en)

Publications (1)

Publication Number Publication Date
DE138392C true DE138392C (en)

Family

ID=406203

Family Applications (1)

Application Number Title Priority Date Filing Date
DENDAT138392D Active DE138392C (en)

Country Status (1)

Country Link
DE (1) DE138392C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5338222A (en) * 1993-02-01 1994-08-16 Hubbell Incorporated Clamping assembly for electrical cables

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5338222A (en) * 1993-02-01 1994-08-16 Hubbell Incorporated Clamping assembly for electrical cables

Similar Documents

Publication Publication Date Title
DE138392C (en)
DE463840C (en) Production of metal phosphides
DE638595C (en) Recovery of the chlorine bound to iron by the chlorination of ores containing iron sulfide in order to obtain the sulfur
DE485070C (en) Manufacture of fertilizers
DE1667375C3 (en) Process for the production of difluorophosphoric acid and phosphoryl fluoride
DE538548C (en) Removal of phosphorus and hydrogen phosphide from gases
DE1065435B (en) Process for the production of powdery, easily spreadable phosphate fertilizers
DE539172C (en) Extraction of nitrogen oxide from the gas mixture formed during the production of potassium nitrate by the reaction of potassium chloride with nitric acid and containing mainly nitrosyl chloride and chlorine in addition to inert gases
DE533857C (en) Process for the preparation of fertilizers consisting essentially of alkali metal phosphates
DE106716C (en)
DE480905C (en) Representation of alkali cyanides from calcium cyanamide
DE532991C (en) Manufacture of tungsten metal
AT136817B (en) Process for the production of tungsten metal.
DE405311C (en) Extraction of alkali sulphides
DE552007C (en) Manufacture of potassium nitrate from aluminum nitrate and potassium chloride
DE3203120C2 (en)
DE695788C (en) Process for the treatment of substances containing tantalum and niobium
DE495793C (en) Process for the preparation of magnesium phosphate
DE641746C (en) Process for the production of cyanides
AT128307B (en) Process for the production of anhydrous aluminum chloride.
DE2545220A1 (en) PROCESS FOR THE PROCESSING OF INACTIVE ANTIMONE HALOGENIDE CATALYSTS INTO Aqueous ANTIMONE III HALOGENIDE SOLUTIONS
AT201569B (en) Process for the enrichment or separation of the elements niobium and tantalum
AT126559B (en) Process for the production of phosphorus-halogen compounds.
DE652445C (en) Process for the production of white lead
DE752867C (en) Process for the preparation of acyclic acetylene polymers