US2031179A - Method of evaporating aqueous hydrochloric acid - Google Patents

Method of evaporating aqueous hydrochloric acid Download PDF

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Publication number
US2031179A
US2031179A US754280A US75428034A US2031179A US 2031179 A US2031179 A US 2031179A US 754280 A US754280 A US 754280A US 75428034 A US75428034 A US 75428034A US 2031179 A US2031179 A US 2031179A
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US
United States
Prior art keywords
hydrochloric acid
phosphoric acid
acid
aqueous hydrochloric
evaporating
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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
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US754280A
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English (en)
Inventor
Raschig Klaus
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Dr F Raschig GmbH
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Dr F Raschig GmbH
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Filing date
Publication date
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Publication of US2031179A publication Critical patent/US2031179A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B7/00Halogens; Halogen acids
    • C01B7/01Chlorine; Hydrogen chloride

Definitions

  • Apparatus of tungsten, tantalum and so forth are therefore used in practice only'to a limited extent, and the object of the present invention is to make possible the evaporation oi aqueous hydrochloric acid in evaporation vessels made of relatively cheap and easily workable metals.
  • an apparatus suitable for evaporating aqueous hydrochloric acid must fulfil the fol- 5 lowing conditions: it must on the one hand be made of a technically easily accessible and workable metal and it must moreover be of normal kind of construction and so must be capable of being heated with steam.
  • the heating is advantageously efiected by heating the upper part of the evaporating apparatus by means of steam tubes welded upon or fitted on, which tubes are well heat insulated on the outside.
  • a temperature is maintained which lies above the temperature of condensation of the hydrochloric acid, that is, at normal pressure, above 110 C.
  • the precipitated alkaline earth metal sulphate forms a suspension in the phosphoric acid which suspension together with the copper chloride resulting from a certain not entirely avoidable corrosion of the apparatus, and likewise forming a suspension in the phosphoric acid, and other impurities contained in the hydrochloric acid. would gradually render the phos- .phoric acid unsuitable for carrying out the process, it is recommended to remove the deposit formed in the phosphoric acid in a suitable manner, for example by filtration or centrifuging. and this can be effected periodically or also continuously during the operation, by continuous removal of a small quantity of phosphoric acid which is returned after having been cleansed.
  • the evaporation can be carried out in various ways.
  • the process may be a discontinuous one. in which a mixture of D1 phoric acid and hydrochloric acid is first introduced into the still of the evaporating apparatus and then subjected to evaporation.
  • a continuous method is employed in which concentrated phosphoric acid, which-may if desired contain some barium chloride, is introduced into the-evaporating vessel, this is then heated and then with continued vigorous heating the aqueous hydrochloric acid. preferably prewarmed. is caused tofiow into the hot phosphoric acid.
  • the concentration ofthe phosphoric acid employed can be suitably selected within wide limits, with corresponding regulation of the heat-- ing and corresponding regulation of the quantity of hydrochloric acid flowing in, for the final concentration adjusts itself automatically in the aosmvc course of the'evaporation in dependence on the heating temperature employed.
  • the actual evaporation chamber consists of a horizontal cylindrical vessel of copper having a length of about 3.5 metres and a diameter of about 1.4 metres.
  • the bottom of the vessel is provided with steam tubes which have an external diameter of about 50 mm. and a length of about 80 metres.
  • the strength of the acid is adjustable by variation of the quantity of heating steam or the quantity of hydrochloric acid flowing in as may be desired, it is also possible to start with a weaker or stronger acid.
  • the contents of the boiler are then heated to about 150 centigrade after which with further heating about 1000 kilos of 17% hydrochloric acid are allowed to flow hourly into the phosphoric acid preferably distributed at diiferent places. After attaining the condition of equilibrium the vapours drawn oil. show the same composition as the hydrochloric acid added.
  • A. method evaporating aqueous hydrochloric acid consisting in carrying out the evaporation in an apparatus made of copper in the presence of. phosphoric acid.
  • a method of evaporating aqueous hydrochloric acid consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid of over 60%.
  • a method of evaporating aqueous hydrochloric acid consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid the parts of the apparatus not touched by the phosphoric acid being heated to a'temperature lying above the temperature of condensation for aqueous hydrochloric acid.
  • a method of evaporating aqueous hydrochloric acid, containing and as an impurity consisting in carrying out the evaporation in an apparatus made of copper in the presence of of phosphoric acid to which salts of metals are added which are soluble in excess phosphoric acid and which form with sulphuric acid salts difilcultly soluble in phosphoric acid.
  • a method of evaporating aqueous hydrochloric acid containing sulfuric acid as an impurity consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid to which alkaline earth metal salts which are soluble in excess phosphoric acid are added.
  • a method of evaporating aqueous hydrochloric acid containing sulfuric acid as an impurity consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid to which alkaline earth metal chlorides are added.
  • a method of evaporating aqueous hydrochloric acid consisting in carrying out the evaporation in 'a continuous process in an apparatus made of copper inthe presence of phosphoric acid.
  • a method of evaporating aqueous hydrochloric acid containing sulfuric acid as an impurity consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid to which are added salts of metals which are soluble in excess phosphoric acid and which with sulphuric acid form salts which are diflicultly soluble in phosphoric acid the deposits which form and which are difllcultly soluble in phosphoric acid being removed by filtration.
  • a method of evaporating aqueous hydrochloric acid containing sulfuric acid as an impurity consisting in carrying out the evaporation in an apparatus made of copper in the presence of phosphoric acid to which are added salts of metals which are soluble in excess phosphoric acid and which with sulphuric acid form salts which are dlfilcultly soluble in phosphoric acid, the deposits which form and which are diflicultly soluble 1 in phosphoric acid being continuously removed by filtration.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
US754280A 1933-11-27 1934-11-22 Method of evaporating aqueous hydrochloric acid Expired - Lifetime US2031179A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DER0089324 1933-11-27

Publications (1)

Publication Number Publication Date
US2031179A true US2031179A (en) 1936-02-18

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ID=7418135

Family Applications (1)

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US754280A Expired - Lifetime US2031179A (en) 1933-11-27 1934-11-22 Method of evaporating aqueous hydrochloric acid

Country Status (3)

Country Link
US (1) US2031179A (fr)
FR (1) FR808504A (fr)
GB (1) GB429816A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2559720A (en) * 1943-02-26 1951-07-10 Fansteel Metallurgical Corp Apparatus for treating gases

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2559720A (en) * 1943-02-26 1951-07-10 Fansteel Metallurgical Corp Apparatus for treating gases

Also Published As

Publication number Publication date
GB429816A (en) 1935-06-06
FR808504A (fr) 1937-02-09

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