GB1033030A - Preparation of inorganic and organic salts - Google Patents

Preparation of inorganic and organic salts

Info

Publication number
GB1033030A
GB1033030A GB3018463A GB3018463A GB1033030A GB 1033030 A GB1033030 A GB 1033030A GB 3018463 A GB3018463 A GB 3018463A GB 3018463 A GB3018463 A GB 3018463A GB 1033030 A GB1033030 A GB 1033030A
Authority
GB
United Kingdom
Prior art keywords
sodium
amine
acid
anion exchanger
prepared
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
GB3018463A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB1033030A publication Critical patent/GB1033030A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0086Processes carried out with a view to control or to change the pH-value; Applications of buffer salts; Neutralisation reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J47/00Ion-exchange processes in general; Apparatus therefor
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/62Methods of preparing sulfites in general
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/26Phosphates
    • C01B25/30Alkali metal phosphates
    • C01B25/301Preparation from liquid orthophosphoric acid or from an acid solution or suspension of orthophosphates
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/46Preparation involving solvent-solvent extraction
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01DCOMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
    • C01D5/00Sulfates or sulfites of sodium, potassium or alkali metals in general
    • C01D5/14Preparation of sulfites

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A metal or ammonium salt of an acid HX which has a dissociation constant higher than 1 x 10-6 is prepared by reacting either HX in the presence of a water-insoluble weak base anion exchanger, or said anion exchanger in the form of a salt with HX, with a metal or ammonium salt of an acid HY, HY having a dissociation constant greater than that of HX. Specified acids HX are sulphurous and phosphoric acids, the metal salts of HY may be sodium chloride, nitrate or sulphate and other specified metal ions are Li, K and Cs. The anion exchanger may be a liquid amine containing 8-25 carbon atoms, and may be a tert.-alkyl primary amine, a secondary amine or a tertiary amine. Such liquid amines are preferably dissolved in an inert water-insoluble solvent, e.g. a hydrocarbon such as kerosene, in the concentration range 5-50%. Less desirably, solid anion exchangers, e.g. those prepared by chloromethylating and aminating a cross-linked aryl hydrocarbon polymer, particularly copolymers of styrene and divinyl benzene, or those prepared by the aminolysis of a cross-linked alkyl acrylate polymer, may be used. Sodium bisulphite may be prepared by agitating an aqueous solution of NaCl with a solvent solution of the amine present in e.g. 33% molar excess and bubbling SO2 through the mixture. The bisulphite may be recovered from the aqueous phase by evaporation, or converted to sodium sulphite by contacting the solution with the free base form of the amine. Sodium dihydrogen phosphate may be prepared by equilibrating phosphoric acid in, e.g., 30% solution with a 33% molar excess of amine and added the stoichiometric quantity of NaCl, or the three reagents may be mixed together. Partial conversion of NaH2PO4 to Na2HPO4 may be achieved by the process of the invention. The anion exchanger may be regenerated with sodium carbonate, sodium hydroxide or ammonia or, particularly in the case of the liquid resins, with an aqueous suspension of lime.ALSO:A metal or ammonium salt of an acid HX which has a dissociation constant higher than 1 x 10-6 is prepared by reacting either HX in the presence of a water-insoluble weak base anion exchanger, or said anion exchanger in the form of a salt with HX, with a metal or ammonium salt of an acid Hy, the dissociation constant of Hy being higher than that of HX. Examples describe the preparation of sodium acid tartrate, sodium citrate, sodium acid malate, sodium formate, sodium acetate and sodium succinate from stoichiometric amounts of sodium chloride solution and the appropriate acid using a 33% molar excess of the anion exchanger. Other metal salts of Hy may be sodium nitrate or sulphate. Other specified metal ions are Li, K and Cs. The anion exchanger may be a liquid amine having 8-25 carbon atoms, and may be a tert.-alkyl primary amine, or a secondary amine, or a tertiary amine. Such liquid amines are preferably dissolved in an inert water-insoluble solvent, e.g. a hydrocarbon such as kerosene, in a concentration of 5-50%. Less desirably solid anion exchangers may be used, e.g. those prepared by chloromethylating and aminating a cross-linked aryl hydrocarbon polymer particularly co-polymers of styrene and divinylbenzene, or those prepared by the aminolysis of a crosslinked alkyl acrylate polymer. The exchangers may be regenerated with sodium carbonate, sodium hydroxide, ammonia or, particularly in the case of the liquid exchangers, an aqueous suspension of lime.
GB3018463A 1963-01-31 1963-07-30 Preparation of inorganic and organic salts Expired GB1033030A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US25522263A 1963-01-31 1963-01-31

Publications (1)

Publication Number Publication Date
GB1033030A true GB1033030A (en) 1966-06-15

Family

ID=22967375

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3018463A Expired GB1033030A (en) 1963-01-31 1963-07-30 Preparation of inorganic and organic salts

Country Status (5)

Country Link
BE (1) BE638465A (en)
CH (1) CH439249A (en)
ES (1) ES291597A1 (en)
GB (1) GB1033030A (en)
NL (1) NL299016A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0248256A2 (en) * 1986-06-04 1987-12-09 Haifa Chemicals Ltd. Process for the manufacture of monopotassium phosphate
WO2000018717A1 (en) * 1998-09-25 2000-04-06 Kemira Chemicals Oy Method for manufacturing alkali metal or alkaline-earth metal formate
EP1659197A1 (en) * 2004-11-18 2006-05-24 Nederlandse Organisatie voor toegepast-natuurwetenschappelijk onderzoek TNO Process for the recovery of acids

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3443889A (en) * 1964-08-17 1969-05-13 Kaiser Aluminium Chem Corp Method of synthesis of alkali metal salts
US3318867A (en) * 1964-08-20 1967-05-09 Upjohn Co Process for separating nitrogen-basic materials from aqueous solution

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0248256A2 (en) * 1986-06-04 1987-12-09 Haifa Chemicals Ltd. Process for the manufacture of monopotassium phosphate
EP0248256A3 (en) * 1986-06-04 1988-03-23 Haifa Chemicals Ltd. Process for the manufacture of monopotassium phosphate
WO2000018717A1 (en) * 1998-09-25 2000-04-06 Kemira Chemicals Oy Method for manufacturing alkali metal or alkaline-earth metal formate
US6492551B1 (en) 1998-09-25 2002-12-10 Kemira Chemicals Oy Method for manufacturing alkali metal or alkaline-earth metal formate
EP1659197A1 (en) * 2004-11-18 2006-05-24 Nederlandse Organisatie voor toegepast-natuurwetenschappelijk onderzoek TNO Process for the recovery of acids
WO2006054893A2 (en) * 2004-11-18 2006-05-26 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Process for the recovery of acids
WO2006054893A3 (en) * 2004-11-18 2006-07-06 Schappelijk Onderzoek Tno Nl O Process for the recovery of acids

Also Published As

Publication number Publication date
CH439249A (en) 1967-07-15
NL299016A (en)
ES291597A1 (en) 1964-01-01
BE638465A (en)

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