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USH856H - Cation exchange Y zeolites as corrosion inhibitors - Google Patents

Cation exchange Y zeolites as corrosion inhibitors Download PDF

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Publication number
USH856H
USH856H US07/226,020 US22602088A USH856H US H856 H USH856 H US H856H US 22602088 A US22602088 A US 22602088A US H856 H USH856 H US H856H
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US
United States
Prior art keywords
zeolite
zeolites
corrosion
exchanged
composition
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.)
Abandoned
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US07/226,020
Inventor
Leon Kutik
Roger J. Lussier
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WR Grace and Co Conn
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WR Grace and Co Conn
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Filing date
Publication date
Application filed by WR Grace and Co Conn filed Critical WR Grace and Co Conn
Priority to US07/226,020 priority Critical patent/USH856H/en
Application granted granted Critical
Publication of USH856H publication Critical patent/USH856H/en
Abandoned legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08—Anti-corrosive paints
    • C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
    • C09D5/084—Inorganic compounds

Definitions

  • This invention relates to the corrosion protection of metals, especially ferrous metals.
  • Y zeolites (free from heavy metals) are ion-exchanged with ions of an alkaline earth metal.
  • the cation exchanged Y zeolites provide corrosion resistance to paints for metals, especially ferrous metals, without health or environmental hazard caused by use of heavy-metal anti-corrosion materials such as lead, chromium, zinc, etc.
  • the primer acts as a sealing layer between the metal and the atmosphere.
  • This primer typically contains rather large quantities of a corrosion-protective material which is intended to inhibit the harmful effect of sulfur, nitrogen, and carbon oxides in the air, as well as water vapor.
  • Materials used for this purpose in the past are the heavy metal compounds, such as red lead, zinc, chromium oxide, and the like. These are generally quite effective; unfortunately they often offer severe health hazards and enduring harm to the environment.
  • U.S. Pat. No. 2,913,419 discloses a sodium aluminum silicate coating on a particle core, ion-exchanged with calcium nitrate, as an anti-corrosion paint additive.
  • U.S. Pat. Nos. 2,848,346, 3,228,784 and 3,509,082 disclose amorphous sodium aluminosilicate zeolite pigments and pigment extenders which may be exchanged with cations such as hydrogen, lithium, calcium, barium, ammonium or cadmium.
  • U.S. Pat. No. 3,899,624 discloses ion exchange resins containing zinc as anti-corrosion additive for paints.
  • U.S. Pat. No. 4,687,595 discloses making corrosion-inhibiting particles comprising binding calcium ions to particles of silica or alumina of a certain surface area, followed by heating and water removal.
  • U.K. Pat. No. 1,503,153 discloses zeolites ion-exchanged with heavy metals as corrosion-inhibitors for paints.
  • the invention is directed to a paint composition containing an alkaline earth metal exchanged Y zeolite as an anti-corrosion additive.
  • the cation exchanged type zeolite is free from anti-corrosion heavy metals such as zinc, lead, and chromium.
  • the invention includes the coatings resulting from the use of these paints, articles coated with the paints, and the method of rendering a paint non-corrosive by incorporating our treated zeolites into the paint.
  • paint is used in the generic sense and includes all liquid coating materials intended for application as protective coatings to surfaces, especially metal surfaces. Primers, sealants, and like coatings for iron, steel, and other ferrous metals are especially contemplated.
  • paint also includes varnishes, enamels, and lacquers; pigmented and non-pigmented vehicles; and both oil- and water-based compositions.
  • Binders in these paints include drying oils, alkyd resins, epoxy resin esters, polyurethanes, phenol resins, urea resins, melamine resins, chlorinated rubbers, epoxide resins, polyamides, polyvinyl acetate, polyvinyl butyral, polyvinylidene fluoride, polyacrylic acid esters, and the like.
  • heavy metals we mean those metals (as their compounds) customarily used in paint to inhibit corrosion on ferrous surfaces, such as Zn, Pb, Co, Cr and Mn.
  • the cation exchanged Y zeolite which is used in the preparation of the paint compositions contemplated herein is obtained by ion-exchanging a Y zeolite (NaY), also referred to as Type Y crystalline aluminosilicate zeolite or synthetic faujasite, having the mol ratio chemical formula:
  • H + /Na 2 O Al 2 O 3 : 3 to 50 SiO 2 , with a solution of the desired alkaline earth metal cation (preferably Ca ++ , Mg ++ and/or Ba ++ ).
  • the Y zeolite precursor zeolites may comprise a sodium Y zeolite (NaY) of the type described in U.S. Pat. No. 3,130,007, or alternatively the Y zeolite may comprise a thermally/chemically modified ultrastable Y zeolite as described in U.S. Pat. No. 3,293,192 and 3,449,070 (USY) a unit cell dimension of about 24.2 to 24.6 ⁇ .
  • NaY sodium Y zeolite
  • USY 3,449,070
  • the cation exchanged Y zeolites have from about 10 to 99 percent of the alkali metal and/or hydrogen cations substituted by desired metal cations.
  • These exchanged Y zeolites are referred to herein as CaNaY, Mg H NaY, etc. to indicate the type of cation exchange achieved.
  • the cation exchanged Y zeolites are incorporated in paint compositions in amounts ranging from about 1 to 20 weight percent of the composition and more preferably from about 2 to 10 weight percent.
  • the cation exchanged Y zeolite is comminuted, i.e. milled or ground, to a particle size range of 50 to 2 microns.
  • the grinding of the Y zeolite component may take place prior to or during addition to the paint formulation.
  • a sodium Y zeolite (NaY) having a silica to alumina ratio of about 4.5 and containing about 13 weight percent Na 2 O is reacted with an aqueous exchange solution of alkali earth metal salt.
  • the exchange solution may contain from about 1 to 25 weight percent of the desired metal salt.
  • the exchange procedure from about 2 to 10 parts exchange solution is combined with each part NaY at a temperature of 20° to 100° C. during which from 10 to 99 weight percent of the initial Na cation is substituted by alkaline earth metal cation.
  • the resulting exchanged Y zeolite has the mol composition: 2 to 25 MO: 0.1 to 10 Na 2 O:Al 2 O 3 :3 to 50 SiO 2 wherein M represents Ca, Mg, and/or Ba.
  • the above described general procedure may be conducted using a variety (including mixtures) of alkaline earth metal salt solutions and various Y zeolites such as USY, HY zeolites as well as NaY zeolites.
  • Sample A comprises a hydrogen/sodium form of ultrastable zeolite Y (USY) which is exchanged to obtain various alkaline earth metal cation exchanged forms of USY.
  • USY ultrastable zeolite Y
  • the ultrastable zeolite Y is prepared by ammonium exchange of a 5.0 SiO 2 /Al 2 O 3 ratio zeolite Y to about 3.8 weight percent Na 2 O, and then calcining in the presence of steam at about 732° C.
  • Sample B was prepared by mixing 1000 g of USY (Sample A) in an exchange solution containing 1,798 g
  • Sample C was prepared by adding 42.0 g magnesium oxide (MgO) to 2 1 H 2 O, boiling one hour to hydrate the magnesia and then diluting to 4.0 1. To the above solution 1,000 g dry basis of USY (Sample A) was added, the slurry aged 1/2 hour at 66° C., filtered, washed on the filter with 2 1 16° C. H 2 O and dried overnight at 138° C.
  • MgO magnesium oxide
  • Sample D was prepared by exchanging 1,000 g (dry basis) USY (Sample A) in a solution containing 10,000 g H 2 O and 1,000 g barium chloride for 1/2 hour at 66° C., filtered and rinsed on the filter with 2 1 66° C. H 2 O. The exchange was repeated, the slurry filtered, washed with 8 1 66° C. H 2 O and dried overnight at 138° C.
  • Alkyd primers were prepared using the following ingredients:
  • the above mixture was dispersed on a high speed mixer for 15 minutes and milled to a particle size of 37 microns. Then the following ingredients were added with mixing.
  • the resulting coatings were then applied to phosphated steel panels at a dry film thickness of approximately 1.1 mils.
  • the coated panels were then scribed and subjected to the standard salt spray test (ASTM-B117) for 500 hours. Results are as follows.
  • Another oil alkyd primer was prepared with the following formulation:
  • the primers were at a film thickness of three mils on an untreated street panel, scribed, and exposed for nine months in Curtis Bay, Md. (near Baltimore) at a 45' south elevation.
  • the area is a highly industralized marine environment.
  • the primer was applied by spraying on 1303 galvanized steel to a dry film thickness of 0.4 mils. It was baked to a peak metal temperature of 450° F. for one minute and scribed. The various primers were exposed 1000 hours in the salt spray test (ASTM-B117). The amount of corrosion inhibitor was held constant in this test at 4.3 weight percent.
  • a group of metal exchanged sodium Y zeolites (NaY) of the present invention were prepared as follows:
  • Mg/NaY (3.9 weight percent Na 2 O-6.0 weight percent MgO) was prepared by adding 500 g dry basis (670.9 g as is) of Na-Y zeolite to 2.5 l 150° F. H 2 O containing 203.3 g magnesium chloride hydrate (MgCl 2 .6H 2 O) for one-half hour at 150° F., filtering and washing twice with 2.5 l 150° F. H 2 O. The exchange was repeated and the sieve then washed three times with 2.5 l 150° F. H 2 O. After calcination for 1 hour at 1000° F., the exchange was repeated once again and the filter cake dried overnight at 250° F.
  • MgCl 2 .6H 2 O magnesium chloride hydrate
  • Ba/Na Y (0.8 weight percent Na 2 O-22.5 weight percent BaO) was prepared in the same way except that 256.1 g barium chloride hydrate (BaCl 2 .2H 2 O) was used for each of the three exchanges.
  • Ca/Na Y (0.05 weight percent Na 2 O-9.0 weight percent CaO) was also prepared in the same way as the Mg/Na Y except that 111 g anhydrous calcium chloride was used for each of the three exchanges.
  • a typical epoxy polyamide maintenance primer with the following composition was prepared and applied to sand blasted steel panels:

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

Zeolites free from heavy metal cations are ion-exchanged with alkaline earth metal cations. The exchanged zeolites provide corrosion resistance to paints for metals, especially ferrous metals, without environmental hazard caused by use of heavy-metal anti-corrosion materials such as lead, chromium, zinc, etc.

Description

FIELD OF THE INVENTION
This invention relates to the corrosion protection of metals, especially ferrous metals.
SUMMARY OF THE INVENTION
Y zeolites (free from heavy metals) are ion-exchanged with ions of an alkaline earth metal. The cation exchanged Y zeolites provide corrosion resistance to paints for metals, especially ferrous metals, without health or environmental hazard caused by use of heavy-metal anti-corrosion materials such as lead, chromium, zinc, etc.
Background of the Invention
In order to protect iron and steel objects which are exposed to atmospheric corrosion, for example, automobiles, railroad equipment, ships, bridges, storage tanks, and the like, it is routine to coat them with several layers of paints, the first of which, the primer, acts as a sealing layer between the metal and the atmosphere. This primer typically contains rather large quantities of a corrosion-protective material which is intended to inhibit the harmful effect of sulfur, nitrogen, and carbon oxides in the air, as well as water vapor. Materials used for this purpose in the past are the heavy metal compounds, such as red lead, zinc, chromium oxide, and the like. These are generally quite effective; unfortunately they often offer severe health hazards and enduring harm to the environment.
Extensive attempts have been made to develop anti-corrosion materials free from heavy metals.
U.S. Pat. No. 2,913,419 discloses a sodium aluminum silicate coating on a particle core, ion-exchanged with calcium nitrate, as an anti-corrosion paint additive.
U.S. Pat. Nos. 2,848,346, 3,228,784 and 3,509,082 disclose amorphous sodium aluminosilicate zeolite pigments and pigment extenders which may be exchanged with cations such as hydrogen, lithium, calcium, barium, ammonium or cadmium.
U.S. Pat. No. 3,899,624 discloses ion exchange resins containing zinc as anti-corrosion additive for paints.
U.S. Pat. No. 4,419,137 (British Petroleum Co.) discloses silica gel ion-exchanged with various metals as corrosion-inhibitors for paints.
U.S. Pat. No. 4,687,595 discloses making corrosion-inhibiting particles comprising binding calcium ions to particles of silica or alumina of a certain surface area, followed by heating and water removal.
U.S. Pat. No. 4,738,720 describes anti-corrosive coating compositions which contain calcium exchanged zeolites.
U.K. Pat. No. 1,503,153 discloses zeolites ion-exchanged with heavy metals as corrosion-inhibitors for paints.
DETAILED DESCRIPTION OF THE INVENTION
The invention is directed to a paint composition containing an alkaline earth metal exchanged Y zeolite as an anti-corrosion additive. The cation exchanged type zeolite is free from anti-corrosion heavy metals such as zinc, lead, and chromium. The invention includes the coatings resulting from the use of these paints, articles coated with the paints, and the method of rendering a paint non-corrosive by incorporating our treated zeolites into the paint.
The term "paint" is used in the generic sense and includes all liquid coating materials intended for application as protective coatings to surfaces, especially metal surfaces. Primers, sealants, and like coatings for iron, steel, and other ferrous metals are especially contemplated. The term "paint" also includes varnishes, enamels, and lacquers; pigmented and non-pigmented vehicles; and both oil- and water-based compositions.
Binders in these paints include drying oils, alkyd resins, epoxy resin esters, polyurethanes, phenol resins, urea resins, melamine resins, chlorinated rubbers, epoxide resins, polyamides, polyvinyl acetate, polyvinyl butyral, polyvinylidene fluoride, polyacrylic acid esters, and the like.
By heavy metals we mean those metals (as their compounds) customarily used in paint to inhibit corrosion on ferrous surfaces, such as Zn, Pb, Co, Cr and Mn.
The following examples illustrate without limiting the invention.
The cation exchanged Y zeolite which is used in the preparation of the paint compositions contemplated herein is obtained by ion-exchanging a Y zeolite (NaY), also referred to as Type Y crystalline aluminosilicate zeolite or synthetic faujasite, having the mol ratio chemical formula:
H+ /Na2 O: Al2 O3 : 3 to 50 SiO2, with a solution of the desired alkaline earth metal cation (preferably Ca++, Mg++ and/or Ba++).
The Y zeolite precursor zeolites may comprise a sodium Y zeolite (NaY) of the type described in U.S. Pat. No. 3,130,007, or alternatively the Y zeolite may comprise a thermally/chemically modified ultrastable Y zeolite as described in U.S. Pat. No. 3,293,192 and 3,449,070 (USY) a unit cell dimension of about 24.2 to 24.6 Å.
Subsequent to exchange with aqueous solution of metal cation salts such as magnesium, calcium, barium chlorides, sulfates and nitrates, the cation exchanged Y zeolites have from about 10 to 99 percent of the alkali metal and/or hydrogen cations substituted by desired metal cations. These exchanged Y zeolites are referred to herein as CaNaY, Mg H NaY, etc. to indicate the type of cation exchange achieved.
The cation exchanged Y zeolites are incorporated in paint compositions in amounts ranging from about 1 to 20 weight percent of the composition and more preferably from about 2 to 10 weight percent.
In order to obtain suitable performance as an anti-corrosion pigment the cation exchanged Y zeolite is comminuted, i.e. milled or ground, to a particle size range of 50 to 2 microns. The grinding of the Y zeolite component may take place prior to or during addition to the paint formulation.
In a typical procedure for preparing the cation exchanged Y zeolite used in the present invention, a sodium Y zeolite (NaY) having a silica to alumina ratio of about 4.5 and containing about 13 weight percent Na2 O is reacted with an aqueous exchange solution of alkali earth metal salt. The exchange solution may contain from about 1 to 25 weight percent of the desired metal salt. During the exchange procedure from about 2 to 10 parts exchange solution is combined with each part NaY at a temperature of 20° to 100° C. during which from 10 to 99 weight percent of the initial Na cation is substituted by alkaline earth metal cation. The resulting exchanged Y zeolite has the mol composition: 2 to 25 MO: 0.1 to 10 Na2 O:Al2 O3 :3 to 50 SiO2 wherein M represents Ca, Mg, and/or Ba.
The above described general procedure may be conducted using a variety (including mixtures) of alkaline earth metal salt solutions and various Y zeolites such as USY, HY zeolites as well as NaY zeolites.
EXAMPLE I
Preparation of the various exchanged Y zeolites used in the subsequent Examples herein is described as follows:
Sample A comprises a hydrogen/sodium form of ultrastable zeolite Y (USY) which is exchanged to obtain various alkaline earth metal cation exchanged forms of USY. The ultrastable zeolite Y is prepared by ammonium exchange of a 5.0 SiO2 /Al2 O3 ratio zeolite Y to about 3.8 weight percent Na2 O, and then calcining in the presence of steam at about 732° C.
Sample B was prepared by mixing 1000 g of USY (Sample A) in an exchange solution containing 1,798 g
of a 42 percent CaCl2 solution and 10,000 g H2 O for 1/2 hour at 66° C. The slurry was filtered and washed with 8 1 66° C H2 O. The exchange and wash steps were repeated, and the sample was dried overnight at 138° C.
Sample C was prepared by adding 42.0 g magnesium oxide (MgO) to 2 1 H2 O, boiling one hour to hydrate the magnesia and then diluting to 4.0 1. To the above solution 1,000 g dry basis of USY (Sample A) was added, the slurry aged 1/2 hour at 66° C., filtered, washed on the filter with 2 1 16° C. H2 O and dried overnight at 138° C.
Sample D was prepared by exchanging 1,000 g (dry basis) USY (Sample A) in a solution containing 10,000 g H2 O and 1,000 g barium chloride for 1/2 hour at 66° C., filtered and rinsed on the filter with 2 1 66° C. H2 O. The exchange was repeated, the slurry filtered, washed with 8 1 66° C. H2 O and dried overnight at 138° C.
The chemical analysis of the above exchanged Y zeolites is given in Table I.
                                  TABLE I                                 
__________________________________________________________________________
CHEMICAL ANALYSES OF ZEOLITES USED AS CORROSION                           
INHIBITORS FOR PRIMER COATINGS                                            
           Sample                                                         
           A     B      C      D                                          
           Composition                                                    
           Na/H USY                                                       
                 Ca/Na USY                                                
                        Mg/Na USY                                         
                               Ba/Na USY                                  
__________________________________________________________________________
TV (wt. %) 15.42 8.54   11.50  7.54                                       
Na.sub.2 O (wt. %)                                                        
            0.75 0.75    3.62  0.77                                       
SiO.sub.2 (wt. %)                                                         
           74.88 --     --     --                                         
Al.sub.2 O.sub.3 (wt. %)                                                  
           22.97 --     --     --                                         
Surface Area, m.sup.2 /gm                                                 
           --    815    886    --                                         
Metal Oxide (wt. %)                                                       
           --    3.19 (CaO)                                               
                        2.78 (MgO)                                        
                               7.13 (BaO)                                 
__________________________________________________________________________
EXAMPLE II
Alkyd primers were prepared using the following ingredients:
______________________________________                                    
                Parts by Weight                                           
______________________________________                                    
Linseed/Soya Alkyd                                                        
                  15.9                                                    
Organic/Smectite Clay                                                     
                  2.0                                                     
Soya Lecithin     .3                                                      
Mineral Spirits   2.8                                                     
Corrosion Inhibitor (as                                                   
                  4.5                                                     
identified in TABLE II)                                                   
Magnesium Silicate                                                        
                  14.0                                                    
Red Iron Oxide    24.8                                                    
______________________________________
The above mixture was dispersed on a high speed mixer for 15 minutes and milled to a particle size of 37 microns. Then the following ingredients were added with mixing.
______________________________________                                    
Linseed/Soya Alkyd                                                        
                  28.2                                                    
6% Cobalt Napthenate                                                      
                  .3                                                      
6% Manganese Napthenate                                                   
                  .2                                                      
6% Zirconium Napthenate                                                   
                  .6                                                      
Anti Skinning Agent                                                       
                  .1                                                      
Mineral Spirits   6.3                                                     
______________________________________
The resulting coatings were then applied to phosphated steel panels at a dry film thickness of approximately 1.1 mils. The coated panels were then scribed and subjected to the standard salt spray test (ASTM-B117) for 500 hours. Results are as follows.
              TABLE II                                                    
______________________________________                                    
Test No.                                                                  
        Corrosion Inhibitor                                               
                         Creepage from Scribe                             
______________________________________                                    
1       Ba/Na USY (Sample D)                                              
                         1/16"                                            
2       Na/H USY (Sample A)                                               
                         1/8" 8F blisters                                 
3       Ca/Na USY (Sample B)                                              
                         1/16"                                            
4       Sodium Type A Zeolite                                             
                         1/8" 8F blisters                                 
5       Hydrotalcite     1/16"                                            
______________________________________
The above data indicates that in test Nos. 1 and 3 the Ba/Na USY and Ca/Na USY corrosion inhibitors of the present invention are similar in effectiveness to the prior art inhibitor, Hydrotalcite. Na/H USY and sodium type A zeolite, which are not corrosion inhibitors of the present invention, are ineffective.
EXAMPLE III
Another oil alkyd primer was prepared with the following formulation:
______________________________________                                    
                 Parts by Weight                                          
______________________________________                                    
Long Oil Soya Alkyd                                                       
                   11.5                                                   
Lecithin           0.47                                                   
Iron Oxide 1301    8.16                                                   
Dolomite           6.70                                                   
Barytes            18.50                                                  
Calcium Carbonate  2.55                                                   
Corrosion Inhibitor                                                       
                   various                                                
(as identified in TABLE III)                                              
Mineral Spirits    7.57                                                   
______________________________________
The above ingredients were ball milled to a maximum particle size of 37 microns. Then the following ingredients were added:
______________________________________                                    
Castor Wax         0.30                                                   
______________________________________
Mill for an additional 30 minutes and add
______________________________________                                    
Long Oil Soya      27.6                                                   
Mineral Spirits    5.10                                                   
24% Lead Napthenate                                                       
                   0.47                                                   
10% Cobalt Octoate 0.12                                                   
Anti-Skimming Agent                                                       
                   0.10                                                   
______________________________________
The primers were at a film thickness of three mils on an untreated street panel, scribed, and exposed for nine months in Curtis Bay, Md. (near Baltimore) at a 45' south elevation. The area is a highly industralized marine environment.
The following results were obtained:
                                  TABLE III                               
__________________________________________________________________________
                  Wt. % Inhibitor                                         
Table No.                                                                 
      Corrosion Inhibitor                                                 
                  In Primer                                               
                          Creepage from Scribe                            
__________________________________________________________________________
1     Zinc Chromate                                                       
                  19      1/16" Dense blistering                          
                          along scribe                                    
2     Barium Meta-Borate                                                  
                  19      1/16"+ Dense blistering                         
                          along scribe                                    
3     Zinc Phosphate                                                      
                  19      1/16" + Dense blistering                        
                          along scribe                                    
4     Ba/Na USY (Sample D)                                                
                  11      1/16" Medium dense                              
                          blistering along scribe                         
5     Ba/Na USY (Sample D)                                                
                  25      1/16" Few blisters                              
                          along scribe                                    
6     Hydrotalcite                                                        
                  11      3/32" Medium blistering                         
                          along scribe                                    
__________________________________________________________________________
The above results show that the corrosion inhibitor of the present invention (Test Nos. 4 & 5) are equivalent to or better than corrosion inhibitors of the prior art (Test Nos. 1, 2, 3 & 6).
EXAMPLE IV
Another example of this primer study is as follows: An epoxy urea primer such as the type used in the coil coating industry on 1303 galvanized steel was prepared and the corrosion inhibitor was varied. The basic formula is:
______________________________________                                    
Epoxy Urea Coil Primer                                                    
                 Parts per Hundred                                        
______________________________________                                    
Epiclorohydrin bis-phenol resin                                           
                   31.0                                                   
(35% solution)*                                                           
China Clay         14.5                                                   
Corrosion Inhibitor                                                       
                   4.3                                                    
(as identified in TABLE IV)                                               
TiO.sub.2          15.2                                                   
Fumed Silica       0.8                                                    
Cellosolve Acetate 10.8                                                   
Urea Formaldehyde resin                                                   
                   11.3                                                   
Aromatic solvent   9.1                                                    
Organic modified smectite clay                                            
                   0.4                                                    
Di-acetone alcohol 2.6                                                    
______________________________________                                    
 *35 parts Epon 1009 32.5 parts MIBK 32.5 parts Butyl Cellosolve
The primer was applied by spraying on 1303 galvanized steel to a dry film thickness of 0.4 mils. It was baked to a peak metal temperature of 450° F. for one minute and scribed. The various primers were exposed 1000 hours in the salt spray test (ASTM-B117). The amount of corrosion inhibitor was held constant in this test at 4.3 weight percent.
The results are as follows:
              TABLE IV                                                    
______________________________________                                    
                          Creepage   Blister-                             
Table No.                                                                 
        Corrosion Inhibiting Pigment                                      
                          From Scribe                                     
                                     ing*                                 
______________________________________                                    
1       Zinc Hydroxy Phosphite                                            
                          No Change  7F                                   
2       Zinc Hydroxy Phosphite                                            
                          3/16       6MD                                  
3       Basic Lead Silica Chromate                                        
                          No Change  8MD                                  
4       Zinc Phosphate    1/4        8MD                                  
5       Barium Metaborate 3/16       8MD                                  
6       Strontium Chromate                                                
                          No Change  None                                 
7       Ba/Na USY (Sample D)                                              
                          1/8        8M                                   
8       Ca/Na USY (Sample B)                                              
                          3/16       8D                                   
9       Mg/Na USY (Sample C)                                              
                          1/4        6M                                   
______________________________________                                    
 *Evaluated as follows: ASTM D71456
The above results indicate that paint formulations containing corrosion inhibitors of the present invention (Test Nos. 7, 8 & 9) are similar to most of those which contain conventional prior art inhibitors (Test Nos. 1-6).
A group of metal exchanged sodium Y zeolites (NaY) of the present invention were prepared as follows:
Mg/NaY (3.9 weight percent Na2 O-6.0 weight percent MgO) was prepared by adding 500 g dry basis (670.9 g as is) of Na-Y zeolite to 2.5 l 150° F. H2 O containing 203.3 g magnesium chloride hydrate (MgCl2.6H2 O) for one-half hour at 150° F., filtering and washing twice with 2.5 l 150° F. H2 O. The exchange was repeated and the sieve then washed three times with 2.5 l 150° F. H2 O. After calcination for 1 hour at 1000° F., the exchange was repeated once again and the filter cake dried overnight at 250° F.
Ba/Na Y (0.8 weight percent Na2 O-22.5 weight percent BaO) was prepared in the same way except that 256.1 g barium chloride hydrate (BaCl2.2H2 O) was used for each of the three exchanges.
Ca/Na Y (0.05 weight percent Na2 O-9.0 weight percent CaO) was also prepared in the same way as the Mg/Na Y except that 111 g anhydrous calcium chloride was used for each of the three exchanges.
EXAMPLE V
A typical epoxy polyamide maintenance primer with the following composition was prepared and applied to sand blasted steel panels:
______________________________________                                    
Part A                                                                    
Epoxy Resin (Epiclorohydrin bis-phenol)                                   
                         17.2                                             
Methyl isobutyl ketone   2.8                                              
Cellosolve               4.5                                              
Corrosion Inhibitor      41.5                                             
(as identified in TABLE V)                                                
Iron Oxide (Mobay)       1.7                                              
Magnesium Silicate       8.2                                              
Urea Formaldehyde Resin  1.0                                              
Xylol                    8.4                                              
Mica 325 mesh            2.6                                              
Part B                                                                    
Epoxy hardner-polyamide  12.0                                             
______________________________________
The panels were aged for one week and subjected to salt spray exposure. The results are summarized in TABLE V.
                                  TABLE V                                 
__________________________________________________________________________
Epoxy Polyamide Primer - Sand Blasted Steel, 1000 Hours Salt Spray        
                          Creepage                                        
                    Film  from                                            
                    Thickness                                             
                          Scribe                                          
                               Blisters-                                  
Test No.                                                                  
      Inhibitor Wt. %                                                     
                    Mils  (Inches)                                        
                               Appearance                                 
__________________________________________________________________________
1     Zinc Phosphate                                                      
                32  5.5   3/16 4M+- Along Scribe                          
2     Calcium Exchanged                                                   
                23  6.8   1/8  Moderate Staining                          
      Silica                                                              
3     Calcium Exchanged                                                   
                13  6.4   3/32 Slight Staining                            
      Silica                                                              
4     Ca/Na Y   23  4.8   1/8  Moderate Staining                          
5     Ca/Na Y   13  5.8   3/16 Moderate Staining                          
6     Ba/Na Y   23  5.9   3/16 Moderate Staining                          
7     Ba/Na Y   13  5.2   1/8  Slight Staining                            
8     Mg/Na Y   23  6.1   1/8  Slight Staining                            
9     Mg/Na Y   13  4.7   1/8  Slight Staining                            
__________________________________________________________________________
The above results show that the paint formulations containing corrosion inhibitors of the present invention (Test Nos. 4-9) are similar to the formulations which contained prior art corrosion inhibitors (Test Nos. 1-3).

Claims (7)

We claim:
1. A paint composition which contains an alkaline earth metal exchanged Y zeolite, said zeolite being substantially free from heavy metal cations.
2. The composition of claim 1 wherein the zeolite is ultrastable Y zeolite.
3. The composition of claim 1 or 2 wherein the alkaline earth metal cation is a member of the group Mg, Ca, Ba, and mixtures thereof.
4. The composition of claim 3 wherein the amount of alkaline earth cation in the zeolite expressed as oxide is within the range of about 3-25 weight percent.
5. The composition of claim 1 wherein the amount of zeolite is in the range 1 to 20 weight percent.
6. A metal substrate coated with the composition of claim 1.
7. A method for protecting a metal substrate from corrosion which comprises coating the substrate with the composition of claim 1.
US07/226,020 1988-07-29 1988-07-29 Cation exchange Y zeolites as corrosion inhibitors Abandoned USH856H (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5138641A (en) * 1989-04-27 1992-08-11 Advanced Micro Devices, Inc. Bit residue correction in a dlc receiver
US20030230364A1 (en) * 2002-04-29 2003-12-18 Greene Jeffrey Allen Conversion coatings including alkaline earth metal fluoride complexes
US20050176851A1 (en) * 2002-06-12 2005-08-11 Cook Ronald L. Releasable corrosion inhibitor compositions
US20050235873A1 (en) * 2004-04-26 2005-10-27 Tony Gichuhi Synergistic corrosion inhibitor
US20100119736A1 (en) * 2008-10-07 2010-05-13 The Regents Of The University Of California Ambient pressure synthesis of zeolite films and their application as corrosion resistant coatings
US9611396B2 (en) 2012-11-09 2017-04-04 AnCatt Conducting polymer nanoparticle composites
CN110724402B (en) * 2019-11-22 2024-03-08 浙江丰虹新材料股份有限公司 An anticorrosive coating containing ion exchange pigments

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US2848346A (en) 1955-05-16 1958-08-19 Huber Corp J M Production of zeolitic pigments
US2913419A (en) 1956-04-18 1959-11-17 Du Pont Chemical process and composition
GB1015704A (en) 1961-05-31 1966-01-05 Huber Corp J M Paint
US3228784A (en) 1962-01-08 1966-01-11 Huber Corp J M Amorphous hydrogen alumino silicate pigments
US3509082A (en) 1961-05-31 1970-04-28 Huber Corp J M Titanium dioxide pigmented paints extended with synthetic sodium alumino silicate pigment
US3899624A (en) 1973-04-26 1975-08-12 Gen Dynamics Corp Method for protecting surfaces against environmental damage and the resultant products
GB1503153A (en) 1974-04-11 1978-03-08 Hoechst Ag Corrosion protection and corrosion-protective composition
US4220567A (en) 1977-06-15 1980-09-02 Bayer Aktiengesellschaft Stabilizing pigmented lacquers with zeolites
US4419137A (en) 1980-08-09 1983-12-06 The British Petroleum Company Limited Corrosion inhibitors, method of producing and protective coatings containing same
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Publication number Priority date Publication date Assignee Title
US2848346A (en) 1955-05-16 1958-08-19 Huber Corp J M Production of zeolitic pigments
US2913419A (en) 1956-04-18 1959-11-17 Du Pont Chemical process and composition
GB1015704A (en) 1961-05-31 1966-01-05 Huber Corp J M Paint
US3509082A (en) 1961-05-31 1970-04-28 Huber Corp J M Titanium dioxide pigmented paints extended with synthetic sodium alumino silicate pigment
US3228784A (en) 1962-01-08 1966-01-11 Huber Corp J M Amorphous hydrogen alumino silicate pigments
US3899624A (en) 1973-04-26 1975-08-12 Gen Dynamics Corp Method for protecting surfaces against environmental damage and the resultant products
GB1503153A (en) 1974-04-11 1978-03-08 Hoechst Ag Corrosion protection and corrosion-protective composition
US4220567A (en) 1977-06-15 1980-09-02 Bayer Aktiengesellschaft Stabilizing pigmented lacquers with zeolites
US4419137A (en) 1980-08-09 1983-12-06 The British Petroleum Company Limited Corrosion inhibitors, method of producing and protective coatings containing same
US4687595A (en) 1984-06-02 1987-08-18 The British Petroleum Company, P.L.C. Process for producing corrosion inhibiting particles
US4738720A (en) 1986-11-14 1988-04-19 International Minerals & Chemical Corp. Anti-corrosive protective coatings

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5138641A (en) * 1989-04-27 1992-08-11 Advanced Micro Devices, Inc. Bit residue correction in a dlc receiver
US20030230364A1 (en) * 2002-04-29 2003-12-18 Greene Jeffrey Allen Conversion coatings including alkaline earth metal fluoride complexes
US7402214B2 (en) * 2002-04-29 2008-07-22 Ppg Industries Ohio, Inc. Conversion coatings including alkaline earth metal fluoride complexes
US20050176851A1 (en) * 2002-06-12 2005-08-11 Cook Ronald L. Releasable corrosion inhibitor compositions
US6933046B1 (en) 2002-06-12 2005-08-23 Tda Research, Inc. Releasable corrosion inhibitor compositions
US20050235873A1 (en) * 2004-04-26 2005-10-27 Tony Gichuhi Synergistic corrosion inhibitor
US7481877B2 (en) 2004-04-26 2009-01-27 Hammond Group, Inc. Synergistic corrosion inhibitor
US20100119736A1 (en) * 2008-10-07 2010-05-13 The Regents Of The University Of California Ambient pressure synthesis of zeolite films and their application as corrosion resistant coatings
US9611396B2 (en) 2012-11-09 2017-04-04 AnCatt Conducting polymer nanoparticle composites
CN110724402B (en) * 2019-11-22 2024-03-08 浙江丰虹新材料股份有限公司 An anticorrosive coating containing ion exchange pigments

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