CS224993B1 - The solvent extraction of the palladium from solutions of the nitric acid - Google Patents

The solvent extraction of the palladium from solutions of the nitric acid Download PDF

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CS224993B1
CS224993B1 CS668082A CS668082A CS224993B1 CS 224993 B1 CS224993 B1 CS 224993B1 CS 668082 A CS668082 A CS 668082A CS 668082 A CS668082 A CS 668082A CS 224993 B1 CS224993 B1 CS 224993B1
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palladium
nitric acid
solutions
extraction
solvent extraction
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CS668082A
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Czech (cs)
Slovak (sk)
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Fedor Doc Rndr Csc Macasek
Vladimir Doc Rndr Csc Mikulaj
Miroslav Ing Drsc Kyrs
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Fedor Doc Rndr Csc Macasek
Vladimir Doc Rndr Csc Mikulaj
Miroslav Ing Drsc Kyrs
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Application filed by Fedor Doc Rndr Csc Macasek, Vladimir Doc Rndr Csc Mikulaj, Miroslav Ing Drsc Kyrs filed Critical Fedor Doc Rndr Csc Macasek
Priority to CS668082A priority Critical patent/CS224993B1/en
Publication of CS224993B1 publication Critical patent/CS224993B1/en

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Description

Vynález ea týká spósobu rezpúšfadlevej extrakci© paládia z reztekev kyseliny dusičnej.The present invention relates to a process for the smooth extraction of palladium from nitric acid slices.

Extrakcia paládia z dusičnanových reztekev prichádza de úvahy pri spraoúvaní rúd, ale najmá vyherenéhe jadrevéhe paliva· Paládium je jedným z cenných štiepnych preduktev, která vznikájú s vysekým výtažkem a ich tvorba v reaktorech može preslahnuť príredné zdroje· Extrakcia paládia béla vsak doteraz študovaná prevažne z halogenidevéhe prostredia, ako extrakčné činidlá sa používajú tributylfosfát a terciárně aminy· Extrakcia terciárnymi amínami a kvartdrnymi ammenievými selami je možná i z dusičnanového prostredia, pričom vznikajú problémy s neurčitosťou chemického stavu paládia v dusičnanových reztekeoh a vplyvem příměsí na extrakciu·Palladium extraction from nitrate resins comes into consideration in ore management, but the least spent nuclear fuel · Palladium is one of the valuable fission precursors that are produced with high yields and their formation in reactors may overreach resources Extraction with tertiary amines and quaternary ammonium salts is also possible from the nitrate environment, creating problems with the uncertainty of the chemical state of the palladium in nitrate resects and the effect of impurities on the extraction.

Túte nevýhodu v podstatnej miere odstraňuje sposob rezpúsťadlevej extrakcie paládia z roztokov kyseliny dusičnej podlá vynálezu kterého podstata spočívá v tem, že paládium ve ferme kati snového ohelátu sa extrahuje nitrebenzénevými roztokmi halegénderivátev dikarbelidu kobaltitéhe. Xatienevé cheláty sa pripravia z dvejfunkčnýoh ligandov obsahujúcich denárové atomy dusíka a síry ake sú 2-teneyltrifluereaoetén, 1,10-fenantrelín, ,£p?-dipyridyl, hexametyléntetramín alebe fermamidíndisulfid· '^^^řiez/^uzíva poznatek, že nitrebenzénevé roztoky dikarbelidu kebaltitéhe a jeho halegénderivátev extrahujú dobré velké hydrefebne katieny aj ze silné kysléhe prostredia· Ak sa k dusičnanovému rozteku přidá ve vodnej alebe kontaktovanej erganlokej fáze Činidle, kterého molekula alebe anién Lz (z»0, -1) tvoří s paládiem katiénevý chelátThis disadvantage is substantially eliminated by the method of palladium extract extraction from nitric acid solutions according to the invention, which is characterized in that the palladium in the cationic fermate semen is extracted with nitrebenzene solutions of the cobaltite dicarbelide halide derivative. Xatien chelates are prepared from bifunctional ligands containing denar nitrogen and sulfur atoms such as 2-teneyltrifluereaoethene, 1,10-phenanthrelin, n-p-dipyridyl, hexamethylenetetramine or fermamidine disulfide solutions. kebaltite and its halogenated derivatives extract good large hydrephebic cations even from strong acidic environments · When a contacted erganlocase phase is added to the nitrate sparge in the aqueous or contacted phase, a reagent whose molecule or anene L z (z »0, -1) forms cationic chelate with palladium

- hPA2 + LZ v ‘y Pdl/2**Z)+ 224 993 bude sa tente katién efektívne vymieňat za iný katién (H+, Cs+) z erganickej fázy :- hPA 2 + L Z v ' y Pdl / 2 ** Z ) + 224 993, this cation will be effectively exchanged for another cation (H + , Cs + ) from the erganic phase:

ρω(2-ϋ)+ +-^ =_ pJi;<2-í)+ +h+ ρω (2-ϋ) + + - ^ = _ pJi; <2-)) + + h +

V praxi sa može tente peznatek využit na selektívnu extrakoiu paládia pe extrakcii oézia®In practice, this broom can be used for selective palladium extraction for oesium® extraction

Příklad 1Example 1

Reztek 0,1 g.dm^ paládia v 1 M HNO^ sa pri teplete 25 *C extrahuje revnakým ebjemem 0,05 M dibrémderivátu dikarbelidu kebaltitéhe (áalej : Br^DGC) alebe hexaohlérderivátu (áalej : ClgDCC) a 0,05 M teneyltriflueracetenu v zmesi nitrebenzén-chlerid uhličitý (1:1)· Výtažek extrakoie za 1,5 h^d| je 61 % a pe 8 hedináoh 96 %.The slice of 0.1 g.dm @ 2 of palladium in 1 M HNO4 at 25 DEG C. is extracted with a reversible volume of 0.05 M dibarbelide debaritide (hereinafter: Br ^ DGC) or hexaohlererivative (hereinafter: ClgDCC) and 0.05 M teneyltriflueracetene. in a mixture of nitrebenzene-carbonyl chloride (1: 1) · Extraction yield in 1,5 h ^ d | is 61% and pe 8 hedges 96%.

Příklad 2Example 2

Extrahuje sa ake v příklade 1 s revnakým ebjemem 0,01 M 2,2*-dipyridylu a 0,01 M BrgDCC alebe ClgDCC v nitrebenzéne· Pe 10 min extrakoii je výtažek 99 %· řríklad 3Extract with AKE in Example 1 with 0.01 M revnakým ebjemem -dipyridylu 2.2 * and 0.01 M BrgDCC or ClgDCC the nitrebenzéne Pe · 10 min extrakoii extract is 99% · Additional examples of 3

Extrahuje sa ake v příklade 1 s revnakým ebjemem 0,01 M 1,10fenantrelínu + 0,01 M BrgDCC alebe ClgDCC v nitrebenzéne* Výtažek pe 10 minútevej extrakcii je 99 %·Extract as in Example 1 with a reversible volume of 0.01 M 1,10phenanthroline + 0.01 M BrgDCC or ClgDCC in nitrebenzene * The yield for 10 minutes extraction is 99% ·

Příklad 4Example 4

K Pd2+ v 1 M HNO^ sa pri teplete 25 ®C přidá hexametyléntetramín de kencentráoie 0,1 M a extrahuje sa 2 h|d{ nitrebenzénevým reztekem 0,01 M BrgDCC· Výtažek je 57 %·To the Pd 2+ in 1 M HNO 4, at a temperature of 25 ° C, add hexamethylenetetramine with a concentration of 0.1 M and extract for 2 h with a nitrobenzene residue of 0.01 M BrgDCC · Yield 57% ·

-ύPríklaí 5-ύExample 5

224 993224 993

K rezteku ak· v příklade 4 aa přidá fermamidíndieulfiá <· kenoentrácie 2 g.da^ * extrahuje ea 2 k|4 aitrebenzánevým reztekea 0,01 M BrgDGG· Výtažek je 83 %·To the residue, if in Example 4 aa, add fermamidine disulfates <2 k.da ^ *, extracts e 2 k and 4 to 4% by weight of 0.01 M BrgDGG · 83% yield ·

Claims (2)

PREDMBT VYNÁLEZU 224 993 1 Sposeb rozpúžťadlevej extrakcie paládia z reztekev kyse-liny dusičnéj vyznačuj úci sa tým, že paládium ve ferme katie-nevébe chelátu sa extrahuje nitrebenzénevými reztekmi halegén-derivátev dikarbelidu kobaltitébe·BACKGROUND OF THE INVENTION 224 993 1 The process of dissolving palladium extraction from nitric acid residues, characterized in that palladium in the fermentation of chelate is extracted with nitrebenzene residues in halegene derivative dikarbelide cobaltite · 2 Sposeb pedla bědu 1 vyznačujúci sa tým, že katienevé che-láty sa pripravia z dvejfunkčnýoh liffandev obsahujúcich denere-vé aterny dusíka a síry, ake sú 2-teneyltriflueraoetén, 1,10-fenantrelín, Z,£Z-dipyridyl, hexametyléntetramín alebe formamidíndisulfid·2. The method of claim 1, wherein the catalyzed chelates are prepared from two-functional lignandins containing denier and nitrogen, such as 2-teneyltrifluoroethanol, 1,10-phenanthreline, Z, Z-dipyridyl, hexamethylenetetramine or formamidine disulfide. ·
CS668082A 1982-09-17 1982-09-17 The solvent extraction of the palladium from solutions of the nitric acid CS224993B1 (en)

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