Process for treating metal surface

• US 5,204,143 A
• Filed: 04/03/1990
• Issued: 04/20/1993
• Est. Priority Date: 04/03/1989
• Status: Expired due to Term

• Current Assignee: Fujifilm Corporation (Fujifilm Holdings Corporation)
• Original Assignee: Fuji Photo Film Co Limited (Fujifilm Holdings Corporation)
• Inventors: Sekiya, Toshiyuki, Nishimiya, Nobuyuki
• Primary Examiner(s): LUSIGNAN, MICHAEL R
• Application Number:
  US07/503,751
• Time in Patent Office: 1,113 Days
• Field of Search: 427/387, 427/327, 427/388.1, 430/275, 428/457
• US Class Current: 427/387
• CPC Class Codes: B41N 3/038 Treatment with a chromium compound, a silicon compound, a phophorus compound or a compound of a metal of group IVB; Hydrophilic coatings obtained by hydrolysis of organometallic compounds
• CPC Class Codes: C07F 7/003 without C-Metal linkages
• CPC Class Codes: C07F 7/04 Esters of silicic acids
• CPC Class Codes: C07F 7/1804 Compounds having Si-O-C linkages Si-O-acyl linkages C07F7/1896
• CPC Class Codes: Y10T 428/31678 Of metal

Abstract

The present invention relates to a process for treating a metal surface wherein a liquid composition comprising an inorganic polymer is applied to the metal surface. The inorganic polymer is produced by hydrolyzing and then polycondensing, in an organic solvent, an organometallic compound having an organic functional group and a group capable of being hydrolyzed and then polycondensed in an organic solvent.

According to the present invention, the metal surface per se is made chemically reactive by fixing functional groups on the metal surface an is very useful, for example, as a support for making a presensitized lithographic plate.

Claims

1. A process for treating a metal surface comprising providing a liquid composition comprising an inorganic polymer produced by hydrolyzing and then polycondensing an organometallic compound having an organic functional group and a group capable of being hydrolyzed and then polycondensed in an organic solvent under conditions such that said organic functional group is kept unreacted and applying said liquid composition under conditions such that said inorganic polymer is adhered to the metal surface and said organic functional group is kept unreacted and remains on the metal surface.

2. The process of claim 1 wherein said organometallic compound is represented by the general formula:

space="preserve" listing-type="equation">A.sub.m M(OR).sub.n

wherein

A represents an organic functional group,

M represents a metal,

R represents a hydrogen atom or an alkyl group, or a functional group which can be replaced with an alkyl group in an organic solvent, and

m and n each represents a positive integer satisfying 1≦

m+n≦

6 and when m is two or more, A'"'"'s may be the same as or different from each other.

3. The process of claim 2 wherein said functional group A is selected from the group consisting of a hydrogen atom, a hydroxy group;

an alkyl group substituted with a substituent other than an unsubstituted aryl;

an aryl group substituted with a substituent other than an unsubstituted alkyl;

a substituted or unsubstituted propargyl group;

a substituted or unsubstituted alkoxy group;

a silyl group; and

a siloxy group.

4. The process of claim 3 wherein a substitutent on the substituted alkyl, aryl, alkenyl, propargyl or alkoxy group is selected from the group consisting of a halogen atom, an alkyl group, an aryl group, a hydroxy group, an alkoxy group, an aryloxy group, an acyloxy group, a carbamoyloxy group, an alkoxycarbonyloxy group, an acyl group, an alkoxycaronyl group, a carbamoyl group, a carboxy group, a propargyl group, an amino group, an alkylamino group, an acylamino group, a ureido group, a carbamate group, a diazonio group, a diazo group, an azo group, a mercapto group, an alkylthio group, a sulfonyl group, a sulfo group, a cyano group, an isocyanate group, a thiocyanate group, a sulfamoyl group, a nitro group, a silyl group and a siloxy group.

5. The process of claim 3 wherein said functional group A is selected from the group consisting of H--, HO--, CH₂ Cl--, CF₃ --(CF₂ --)₃, HOCH₂ CH₂ CH₂ -- ##STR31##

6. The process of claim 2 wherein said M is selected from the group consisting of Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr, Ba, Sc, Y, rare earth metals, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Nb, Mo, Hf, Ta, W, Ru, Rh, Pd, Ir, Pt, B, Al, Ga, In, Tl, Si, Ge, Sn, Pb, P, As, Sb and Bi.

7. The process of claim 6 wherein said M is Al, Si or Ti.

8. The process of claim 2 wherein said alkyl group as said R is selected from the group consisting of CH₃ --, C₂ H₅ --, n-C₃ H₇ --, i-C₃ H₇ --, n-C₄ H₉ --, sec-C₄ H₉ --, tert-C₄ H₉ -- or a cyclohexyl group.

9. The process of claim 1 wherein said organometallic compound is used together with a compound having the following general formula:

space="preserve" listing-type="equation">M(OR).sub.n

wherein

M is a metal,

R is a hydrogen atom or an alkyl group, or a functional group which can be replaced with an alkyl group in an organic solvent, and

n is a positive integer satisfying 1≦

n≦

6.

10. The process of claim 1 wherein said organometallic compound is selected from the group consisting of H₂ N(CH₂)₂ NH(CH₂)₃ --Si(OCH₃)₃, CH₂ ═

CH--Si(OCOCH₃)₃, CH₂ ═

CH--Si(OC₂ H₅)₃, H₂ N(CH₂)₃ --Si(OC₂ H₅)₃, OCNCH₂ CH₂ CH₂ --Si(OCH₃)₃, ##STR32##

11. The process of claim 1 wherein said organic solvent is selected from the group consisting of methanol, ethanol, i-propanol, hexane, cyclohexane, benzene, toluene, 1,4-dioxane, tetrahydrofuran, methyl ethyl ketone, ethyleneglycol dimethyl ether, ethyleneglycol monomethyl ether, ethyleneglycol diethyl ether, propyleneglycol monomethyl ether, acetylacetone, N,N-dimethylformamide and monoethanol amine.

12. The process of claim 1 wherein the hydrolysis is conducted in the presence of water.

13. The process of claim 1 wherein said metal surface is a pure metal surface of aluminum, iron, copper, titanium, zirconium or the alloy thereof.

14. The process of claim 9 wherein said compound of M(OR)_n is selected from the group consisting of ##STR33##