CS253329B1 - Process for preparring siccative on the base of cobalt compounds - Google Patents
Process for preparring siccative on the base of cobalt compounds Download PDFInfo
- Publication number
- CS253329B1 CS253329B1 CS862309A CS230986A CS253329B1 CS 253329 B1 CS253329 B1 CS 253329B1 CS 862309 A CS862309 A CS 862309A CS 230986 A CS230986 A CS 230986A CS 253329 B1 CS253329 B1 CS 253329B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- cobalt
- solution
- siccative
- preparation
- butanol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- 150000001869 cobalt compounds Chemical class 0.000 title description 3
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 18
- 239000010941 cobalt Substances 0.000 claims abstract description 18
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 17
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000003849 aromatic solvent Substances 0.000 claims abstract description 4
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 4
- 150000001868 cobalt Chemical class 0.000 claims abstract description 4
- 238000002360 preparation method Methods 0.000 claims abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 3
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 claims description 7
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims description 2
- 229940116357 potassium thiocyanate Drugs 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 2
- -1 cobalt monocarboxylic acid salt Chemical class 0.000 abstract 2
- 229910052700 potassium Inorganic materials 0.000 abstract 2
- 239000011591 potassium Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000002274 desiccant Substances 0.000 description 6
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- XVYAXLVMQFDGTK-UHFFFAOYSA-N 1-butoxybutane;ethane-1,2-diol Chemical compound OCCO.CCCCOCCCC XVYAXLVMQFDGTK-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- MIAJZAAHRXPODB-UHFFFAOYSA-N cobalt potassium Chemical compound [K].[Co] MIAJZAAHRXPODB-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Řešení se týká přípravy účinného sikativačního činidla se sníženým obsahem kobaltu. Je řešen technický problém přípravy roztoků sikativačního činidla, obsahujících rhodanokobaltnaté komplexy. Podstata řešení spočívá v tom, že se na roztok kobaltnaté soli monokarboxylové kyseliny o počtu atomů uhlíku 6 až 18 v alifatickém nebo aromatickém rozpouštědle nebo jejich směsi, s obsahem 1 až 10 í kobaltu v sušině působí rodanidem draselným v molárním poměru kobaltnatá sůl/rodanid draselný = 1, v přítomnosti monoalkyléteru ethylenglykolu s alkylem o počtu atomů uhlíku 1 až 4 a/nebo butanoluThe solution relates to the preparation of an effective siccative agents with reduced cobalt content. It is technical problem of preparation of siccativating solutions agents containing rhodanocobalt complexes. The essence of the solution is that it is to a solution of the cobalt monocarboxylic acid salt having carbon numbers of 6 to 18 in the aliphatic or an aromatic solvent or an aromatic solvent thereof mixtures, containing 1 to 10% cobalt in dry matter works with potassium rodanide in a molar ratio cobalt salt / potassium rodanide = 1, in the presence ethylene glycol alkyl monoalkyl ether with the number of carbon atoms 1 to 4 and / or butanol
Description
Vynález se týká způsobu přípravy sikativačního činidla na bázi sloučenin kobaltu.The present invention relates to a process for the preparation of a cicalt compound driers.
Nátěrové hmoty na bázi vysýchavých olejů nebo dehydratovaných či izomerizovanýoh nenasycených mastných kyselin, se sikativuji obvykle sloučeninami kobaltu, nejčastěji isononáty, naftenáty, oktoáty nebo rezináty kobaltnatými. V posledních letech zaznamenává světový trh vzrůstající nedostatek kobaltu, což se projevuje rostoucím trendem cen sloučenin kobaltu.Coating compositions based on drying oils or dehydrated or isomerized unsaturated fatty acids are usually siccated with cobalt compounds, most commonly isononates, naphthenates, octoates or cobalt resinates. In recent years, the world market has experienced an increasing cobalt shortage, which is reflected in an increasing trend in cobalt compound prices.
V oblasti sikativace vysýchavých nátěrových hmot se zatím nepodařilo nalézt plnphodnotnou náhradu za kobaltnaté sikativy, proto vývoj spěje směrem řešení účinných sikativačních činidel se sníženým obsahem kobaltu, jako jsou například ekvimolárni rhodanokobaltnaté komplexy a jejich roztoky. Technologie výroby těchto komplexů nebyla dosud popsána.In the field of the desiccation of desiccant paints, no full replacement for cobalt dicotics has been found so far, therefore the development is heading towards effective cobalt-reduced siccating agents such as equimolar rhodanocobalt complexes and their solutions. Technology of production of these complexes has not been described yet.
Nyní jsme nalezli, že ekvimolárni rhodanokobaltnaté komplexy lze připravit způsobem podle vynálezu spočívající v tom, že na roztok kobaltnaté soli monokarboxylové kyseliny o počtu uhlíku Cj. až C^g v alifatickém či aromatickém rozpouštědle či jejich směsi, s obsahem 1 až 10 % kobaltu v sušině, se působí rhodanidem draselným tak, aby molární poměr kobaltnatá sůl rhodanid draselný ' v přítomnosti monoalkylesterú etylenglykolu s alkylem o počtu uhlíku' 1 až 4, a/nebo butanolu.We have now found that equimolar rhodanocobalt (II) complexes can be prepared by the process of the invention, consisting of a solution of the cobalt salt of a monocarboxylic acid having a carbon number of C 1. In the case of an aliphatic or aromatic solvent or mixtures thereof containing 1 to 10% of cobalt in the dry matter, treatment with potassium rhodanide is carried out so that the molar ratio of cobalt potassium rhodanide in the presence of monoalkyl esters of ethylene glycol with alkyl of 1 to 4; and / or butanol.
Složení rozpouštědel se řídí druhem a charakterem nátěrové hmoty, způsobu zpracováni, skladováni a podobně. Množství použitých rozpouštědel se volí obvykle tak, aby obsah kobaltu ve vyrobeném sikativačním činidle dosahoval nejméně 1 %. Z monoalkyléterů se s výhodou používá monometyléteru, monoetyléteru nebo monobutyléteruetylenglykolu, dále se používají směsi těchto éterů s n-butanolem nebo isobutanolem obsahujícím nejvýše 80 % butanolu. Místo rhodanidu draselného lze v případě potřeby použít i rhodanid sodný nebo amonný, obvykle se však zhoršuje rozpustnost sikativačního činidla v některých typech nátěrových hmot.The composition of the solvents is governed by the nature and nature of the coating composition, the processing, storage and the like. The amount of solvents used is usually selected so that the cobalt content of the desiccant produced is at least 1%. Of the monoalkyl ethers, preferably monomethyl ether, monoethyl ether or monobutyl ether-ethylene glycol is used, and mixtures of these ethers with n-butanol or isobutanol containing at most 80% butanol are used. Sodium or ammonium rhodanide may also be used instead of potassium rhodanide, however, the solubility of the desiccant in some types of paints usually deteriorates.
Na složení výrobku nemá vliv pořadí nasazovaných látek do směšovací nádoby, obvykle je však výhodnější předkládat roztok kobaltnaté soli, popřípadě s rozpouštědly a dávkovat pevný rhodanid. Reakční doba je v podstatě limitována rychlostí rozpouštění rhodanidu v reakční směsí, která je určena jednak složením rozpouštědel a teplotou, jednak intenzitou míchání. Obvykle postačuje k plnému ukončení reakce v rozmezí 20 až 30 °C míchání směsi po dobu 1 hodiny.The composition of the product is not influenced by the order of the substances used in the mixing vessel, but it is usually preferable to present the cobalt salt solution, optionally with solvents, and to dispense solid rhodanide. The reaction time is essentially limited by the rate of dissolution of the rhodanide in the reaction mixture, which is determined both by the composition of the solvents and by the temperature and by the intensity of stirring. Usually, stirring for 1 hour is sufficient to complete the reaction in the range of 20-30 ° C.
Příkla.dlPříkla.dl
Do ploché kádinky objemu 250 ml se naváží 2 g rhodanidu draselného, 23,6 g naftenátu kobaltnatého (obsahujíciho 5 % kobaltu v sušině), 10 g n-butanolu a 5 g monoetyléteru etylenglykolu. Směs se při pokojové teplotě míchá 1 hodinu, kdy je rozpouštění rhodanidu ukončeno. Sikativační činidlo obsahuje 3,26 % kobaltu v sušině.Weigh 2 g of potassium rhodanide, 23.6 g of cobalt naphthenate (containing 5% cobalt in the dry matter), 10 g of n-butanol and 5 g of ethylene glycol monoethyl ether in a 250 ml flat beaker. The mixture was stirred at room temperature for 1 hour when the dissolution of the rhodanide was complete. The desiccant contains 3.26% cobalt in the dry matter.
Příklad 2Example 2
Do ploché kádinky objemu 500 ml se předloží 11,8 g oktoátu kobaltnatého (obsahuje 10 % kobaltu v sušině) a 45,2 g monometyléteru etylenglykolu. Při 25 °C se za mícháni vsypávají 2,0 g rhodanidu draselného, směs se 30 minut míchá, načež se ředí 59,0 g toluenu a míchá se ještě 10 minut. Sikativační činidlo obsahuje 1,05 i kobaltu v sušině.A 500 ml flat beaker was charged with 11.8 g of cobalt octoate (containing 10% cobalt in dry matter) and 45.2 g of ethylene glycol monomethylether. At 25 [deg.] C., 2.0 g of potassium rhodanide are added with stirring, the mixture is stirred for 30 minutes, then diluted with 59.0 g of toluene and stirred for a further 10 minutes. The desiccant contains 1.05 cobalt in dry matter.
Příklad 3Example 3
Do ploché kádinky se odváži 47,2 g roztoku (obsahujícího 5 % kobaltu jako kovu), 20 g butanolu a 4 g rhodanidu draselného. Míchá se při 25 °C 1,5 hodiny do rozpuštění rhodanidu. Sikativační činidlo obsahuje 3,17 % kobaltu v sušině.Weigh 47.2 g of a solution (containing 5% cobalt metal), 20 g of butanol and 4 g of potassium rhodanide into a flat beaker. Stir at 25 ° C for 1.5 hours to dissolve the rhodanide. The desiccant contains 3.17% cobalt in dry matter.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS862309A CS253329B1 (en) | 1986-04-01 | 1986-04-01 | Process for preparring siccative on the base of cobalt compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS862309A CS253329B1 (en) | 1986-04-01 | 1986-04-01 | Process for preparring siccative on the base of cobalt compounds |
Publications (2)
Publication Number | Publication Date |
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CS230986A1 CS230986A1 (en) | 1987-03-12 |
CS253329B1 true CS253329B1 (en) | 1987-11-12 |
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CS862309A CS253329B1 (en) | 1986-04-01 | 1986-04-01 | Process for preparring siccative on the base of cobalt compounds |
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1986
- 1986-04-01 CS CS862309A patent/CS253329B1/en unknown
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CS230986A1 (en) | 1987-03-12 |
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