US2018066365A1PendingUtilityA1

Pre-rinse containing a quaternary amine for conditioning prior to a conversion treatment

Assignee: HENKEL AG & CO KGAAPriority: May 29, 2015Filed: Nov 1, 2017Published: Mar 8, 2018
Est. expiryMay 29, 2035(~8.8 yrs left)· nominal 20-yr term from priority
C23C 22/78C23F 11/149C23F 11/143C23F 11/141C23F 11/163C23C 22/50
38
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Claims

Abstract

A multi-step process for the anti-corrosive pretreatment of components component formed at least partially from metallic materials wherein first components are subjected to a conditioning wet-chemical treatment with an aqueous composition (A) that contains a salt of a quaternary amine and then to an additional wet-chemical treatment based on water-soluble compounds of the elements Zr, Ti and/or Si, in the course of which treatment a corresponding conversion of the surfaces of the metallic materials takes place, said treatment providing an anti-corrosive primer for additionally applied organic coatings.

Claims

exact text as granted — not AI-modified
1 . A multi-stage method for anti-corrosive pretreatment of components fabricated at least partially from metallic materials, wherein initially:
 i) at least a portion of a surface of a component formed at least partially from metallic materials is brought in contact with an aqueous composition (A) comprising a dissolved and/or dispersed salt of a quaternary organic amine;   and subsequently   ii) at least the same portion of the surface of the component formed at least partially from the metallic materials is brought in contact with an aqueous composition (B) comprising one or more water-soluble compounds of the elements Zr, Ti and/or Si.   
     
     
         2 . The method according to  claim 1 , wherein the quaternary organic amines are selected from heterocyclic compounds comprising at least one quaternary nitrogen heteroatom. 
     
     
         3 . The method according to  claim 2 , wherein the heterocyclic compound comprising at least one quaternary nitrogen heteroatom corresponds to the following chemical formula (I): 
       
         
           
           
               
               
           
         
         wherein functional groups R 1 , R 2  and R 3  are each independently selected from hydrogen; branched or unbranched aliphatic compounds comprising no more than 6 carbon atoms; and a functional group corresponding to:
   —C(CR 4 R 4 ) x —[Z(R 4 ) (p-1) —(CR 4 R 4 ) y ] n —Z(R 4 ) p  
 
 where Z is selected from oxygen or nitrogen; 
 p, in cases where Z is nitrogen, is 2 and otherwise is equal to 1; 
 x and y are each natural numbers from 1 to 4; 
 n is a natural number from 0 to 4; and 
 R 4  is selected from hydrogen, branched aliphatic compounds comprising no more than 6 carbon atoms and unbranched aliphatic compounds comprising no more than 6 carbon atoms; 
 with the proviso that at least one of the functional groups R 2  or R 3  is not selected from hydrogen; and 
 
         Y is a ring-constituting divalent functional group, which comprises no more than 5 bridge atoms, wherein no more than one heterobridge atom different from carbon atoms selected from oxygen, nitrogen or sulfur can be a bridge atom, and the carbon atoms in turn independently of one another are present substituted with functional groups R 1  or with functional groups via which an annulation of aromatic homocyclic compounds having no more than 6 carbon atoms is achieved. 
       
     
     
         4 . The method according to  claim 3 , wherein the ring-constituting divalent functional group Y is selected from ethylene, ethenediyl, 1,3-propanediyl, 1,3-propenediyl, 1,4-butanediyl, 1,4-butenediyl, 1,4-butadienediyl, —CH═N—, —CH 2 —NH—, (N,N-dimethylene)amine, (N-methylene-N-methylylidene)amine, wherein in each case hydrogen covalently bound to a carbon atom can be substituted by the remaining representatives of functional group R 1 . 
     
     
         5 . The method according to  claim 4 , wherein the ring-constituting divalent functional group Y is selected from ethenediyl, 1,4-butadienediyl, —C═N— and (N-methylene-N-methylylidene)amine. 
     
     
         6 . The method according to  claim 1 , wherein the quaternary organic amine is selected from 1,2,3-trimethylimidazolium, 1-methyl-3-methylimidazolium, 1-ethyl-3-methylimidazolium, 1-isopropyl-3-methylimidazolium, 1-propyl-3-methylimidazolium, 1-(n-butyl)-3-methylimidazolium, 1-(isobutyl)-3-methylimidazolium, 1-methoxy-3-methylimidazolium, 1-ethoxy-3-methylimidazolium, 1-propoxy-3-methylimidazolium and mixtures thereof. 
     
     
         7 . The method according to  claim 1 , wherein the aqueous composition (A) in step i) additionally comprises anions comprising no more than 5 carbon atoms and selected from monoalkyl sulfates, monoalkyl sulfonates, dialkyl phosphates and/or dialkyl phosphonates. 
     
     
         8 . The method according to  claim 1 , wherein the quaternary organic amine in the aqueous composition (A) is present in an amount of at least 0.05 g/kg, but no more than 20 g/kg. 
     
     
         9 . The method according to  claim 1 , wherein no conversion layer is generated on the surfaces of the metallic components in step i). 
     
     
         10 . The method according to  claim 1 , wherein the aqueous composition (A) comprises less than 0.05 g/kg of surface-active compounds which are not composed of quaternary organic amines. 
     
     
         11 . The method according to  claim 1 , wherein the aqueous composition (B) in step ii) comprises at least 0.01 g/kg of water-soluble compounds of the elements Zr, Ti or Si, based on the respective element. 
     
     
         12 . The method according to  claim 1 , wherein the aqueous composition (B) in step ii) comprises less than 0.05 g/kg free fluoride. 
     
     
         13 . The method according to  claim 1 , wherein a total proportion of fluorides in the aqueous composition (B) in step ii) is less than 0.05 g/kg. 
     
     
         14 . The method according to  claim 1 , further comprising cleaning and degreasing the component formed at least partially from metallic materials prior to step i), by bringing the component into contact with aqueous compositions comprising surface-active compounds. 
     
     
         15 . The method according to  claim 1 , wherein a rinsing step, and no drying step, takes place between steps i) and ii). 
     
     
         16 . The method according to  claim 1 , wherein the component formed at least partially from metallic materials at least partially comprises surfaces of iron and/or steel, and at least 50%, of the surface of metallic materials of the component is formed of surfaces of the materials iron and/or steel. 
     
     
         17 . The method according to  claim 5 , wherein the quaternary organic amine is selected from 1,2,3-trimethylimidazolium, 1-methyl-3-methylimidazolium, 1-ethyl-3-methylimidazolium, 1-isopropyl-3-methylimidazolium, 1-propyl-3-methylimidazolium, 1-(n-butyl)-3-methylimidazolium, 1-(isobutyl)-3-methylimidazolium, 1-methoxy-3-methylimidazolium, 1-ethoxy-3-methylimidazolium, 1-propoxy-3-methylimidazolium and mixtures thereof. 
     
     
         18 . The method according to  claim 17 , wherein the aqueous composition (A) in step i) additionally comprises anions selected from monoalkyl sulfates and/or monoalkyl sulfonates, said anions comprising no more than 5 carbon atoms.

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