US20080099729A1 - Corrosion inhibiting mixture - Google Patents
Corrosion inhibiting mixture Download PDFInfo
- Publication number
- US20080099729A1 US20080099729A1 US11/588,885 US58888506A US2008099729A1 US 20080099729 A1 US20080099729 A1 US 20080099729A1 US 58888506 A US58888506 A US 58888506A US 2008099729 A1 US2008099729 A1 US 2008099729A1
- Authority
- US
- United States
- Prior art keywords
- mixture
- corrosion inhibiting
- weight
- binding matrix
- salt
- 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
Links
- 238000005260 corrosion Methods 0.000 title claims abstract description 56
- 230000007797 corrosion Effects 0.000 title claims abstract description 56
- 239000000203 mixture Substances 0.000 title claims abstract description 42
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 15
- 239000003112 inhibitor Substances 0.000 claims abstract description 37
- 239000011159 matrix material Substances 0.000 claims abstract description 20
- 229920001944 Plastisol Polymers 0.000 claims abstract description 16
- 239000004999 plastisol Substances 0.000 claims abstract description 16
- 239000011347 resin Substances 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 14
- 239000004593 Epoxy Substances 0.000 claims abstract description 13
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000007788 liquid Substances 0.000 claims abstract description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 13
- 239000004014 plasticizer Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000004848 polyfunctional curative Substances 0.000 claims description 8
- 239000005711 Benzoic acid Substances 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 235000010233 benzoic acid Nutrition 0.000 claims description 5
- -1 amine nitrite salt Chemical class 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 238000004132 cross linking Methods 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 150000002826 nitrites Chemical class 0.000 claims description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 4
- 229920006243 acrylic copolymer Polymers 0.000 claims 2
- 239000012764 mineral filler Substances 0.000 claims 1
- 208000037820 vascular cognitive impairment Diseases 0.000 description 21
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 238000004806 packaging method and process Methods 0.000 description 7
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
- 239000012964 benzotriazole Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007769 metal material Substances 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 4
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 2
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 2
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000013270 controlled release Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229960002446 octanoic acid Drugs 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 1
- OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 1
- SBKDOVGGFMYFDW-UHFFFAOYSA-N 2-(diethylamino)ethanol;octanoic acid Chemical compound CCN(CC)CCO.CCCCCCCC(O)=O SBKDOVGGFMYFDW-UHFFFAOYSA-N 0.000 description 1
- HTFJQCPNSUFMLF-UHFFFAOYSA-N 2-(diethylamino)ethyl decanoate Chemical compound CCCCCCCCCC(=O)OCCN(CC)CC HTFJQCPNSUFMLF-UHFFFAOYSA-N 0.000 description 1
- WUGCLPOLOCIDHW-UHFFFAOYSA-N 2-aminoethanol;benzoic acid Chemical compound [NH3+]CCO.[O-]C(=O)C1=CC=CC=C1 WUGCLPOLOCIDHW-UHFFFAOYSA-N 0.000 description 1
- KWIPUXXIFQQMKN-UHFFFAOYSA-N 2-azaniumyl-3-(4-cyanophenyl)propanoate Chemical compound OC(=O)C(N)CC1=CC=C(C#N)C=C1 KWIPUXXIFQQMKN-UHFFFAOYSA-N 0.000 description 1
- AHLWZBVXSWOPPL-RGYGYFBISA-N 20-deoxy-20-oxophorbol 12-myristate 13-acetate Chemical compound C([C@]1(O)C(=O)C(C)=C[C@H]1[C@@]1(O)[C@H](C)[C@H]2OC(=O)CCCCCCCCCCCCC)C(C=O)=C[C@H]1[C@H]1[C@]2(OC(C)=O)C1(C)C AHLWZBVXSWOPPL-RGYGYFBISA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 239000004921 DEGALAN® Substances 0.000 description 1
- 241000285023 Formosa Species 0.000 description 1
- 241001602688 Pama Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 229940090948 ammonium benzoate Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- DSSYKIVIOFKYAU-UHFFFAOYSA-N camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 description 1
- CIFYUXXXOJJPOL-UHFFFAOYSA-N cyclohexylazanium;benzoate Chemical compound [NH3+]C1CCCCC1.[O-]C(=O)C1=CC=CC=C1 CIFYUXXXOJJPOL-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/02—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in air or gases by adding vapour phase inhibitors
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
Definitions
- This invention relates to improvements in volatile corrosion inhibitors, and more particularly to improvements in volatile corrosion inhibitor delivery devices.
- VCIs volatile corrosion inhibitors
- a known technique for reducing the corrosion of metal articles is to package the articles with a material containing a volatile corrosion inhibitor (“VCI”).
- VCIs function by slowly releasing vapors that contact the surface of the metals.
- the vapor phase corrosion inhibitors envelop the metal article in a non-corrosive atmosphere and retard moisture and oxygen present in the atmosphere from attacking and reacting with the metal surfaces.
- Volatile corrosion inhibitors may be applied by spraying the entire surface of the metal article to be protected, or the metal article itself may be enclosed, packaged or surrounded in or with materials containing VCIs.
- VCIs may be incorporated into a packaging material such as paper and plastic wraps, films, and plastic dunnage.
- VCIs are also known to be incorporated into an emitting device with a binding matrix. Such emitters can be used within closed spaces such as packaging containers, electrical boxes, storage bags, and other enclosures. Different volatile corrosion inhibitors or combinations of volatile corrosion inhibitors may be selected based on the type of metal to be protected, the size of the enclosure, and the length of time that protection is required.
- Known volatile corrosion inhibitor emitting devices have several drawbacks. They are produced in a set shape such as foam strips, compressed pellets, and air permeable containers such as plastic cups with paper tops.
- the set shape may not “fit” an intended application. For example, an emitter may be placed randomly in a packaging container or enclosure or stuck to a surface within the package or enclosure. Many end users do not want loose articles or articles that do not appear to be part of the packaging in the containers they receive.
- generic shapes do not adequately identify the function of the VCI device. Since it is sometimes difficult to clearly distinguish that the device is purposely part of the packaging or the enclosure, it may be misplaced or mistakenly removed. Further, there is the problem of reinserting the device as part of a pack and having to locate it properly.
- VCI packaging devices produced in this way usually contain the active materials in powder or pellet form. These powders and pellets can spill or spread active materials to unwanted areas. In general known emitter devices have insufficient control over the release of the VCIs.
- U.S. Pat. No. 4,124,549 to Hashiudo et al discloses a method for making a corrosion protective film which includes a thermoplastic resin and a volatile corrosion inhibitor mixed together and molded or extruded. Such a product is disadvantages for several of the reasons cited above. In addition, such a thermoplastic composition would result in the loss of many VCIs at the high temperatures needed to form the film.
- a corrosion inhibiting mixture comprising a volatile corrosion inhibitor and a binding matrix, wherein the binding matrix comprises a resin selected from the group of a plastisol, a urethane and an epoxy.
- the mixture is liquid near ambient temperature and irreversibly cured when heated in a temperature range of about 20° C. to 150° C.
- a vapor-phase or volatile corrosion inhibitor emitting device comprises a volatile corrosion inhibitor and a binding matrix.
- This mixture is combined to form a pourable and moldable liquid at relatively low temperatures, most preferably ambient room temperature (about 20° C.).
- the mixture may be poured into a mold of any desired moldable shape and gently heated to about 20° C. to 150° C. In accordance with a highly advantageous feature, this heating cures the mixture, so that reheating will not result in melting. Also, forming and curing the mixture at low temperatures is advantageous in that loss of volatile corrosion inhibitors is reduced.
- a volatile corrosion inhibitor emitting device which can be readily molded or cast, allowing the emitting device to form a shape that fits a particular application. Many current and potential applications for these devices would be substantially improved if the device could be custom fitted to an enclosure, a packaging container or the items being protected from corrosion.
- the volatile corrosion inhibitor emitting device can be readily molded or caste into shapes that are known symbols or company logos. With addition of an appropriate pigment, a specific color can be used for a specific application. Emitters may be formed as a narrow cylinder to protect gun barrels, fish-shaped to protect tackle boxes, a bolt to protect tool boxes, a blue shield to protect ferrous based metals, a red shield to protect electrical boxes, etc.
- VCIs for incorporation into the binding matrix include benzoic acid and inorganic salts of benzoic acid such as sodium benzoate, inorganic nitrite salts such as sodium nitrite, amine nitrite salts such as dicyclohexylamine nitrite, carboxylic acids such as caprylic acid, salts of amines and carboxylic acids such as cyclohexylamine benzoate, monoethanolamine benzoate, diethylethanolamine caprylate, and diethylethanolamine caprate, azoles such as tolyltriazole, benzotriazole and their salts, and salts of molybdenum such as sodium molybdate or an amine molybdate.
- Other volatile corrosion inhibitors suitable for use herein will be readily apparent to those skilled in the art given the benefit of this disclosure.
- the binding matrix preferably satisfies a number of conditions. It should be processable at temperatures low enough that the volatile corrosion inhibitors are not driven off during processing.
- the binding matrix should be able to be readily adjusted to control the emission rate of the volatile corrosion inhibitors. It should be capable of being readily molded or cast into various shapes.
- the binding matrix should have long term durability for extended use applications. It should be permeable enough to allow the corrosion inhibitor(s) to migrate out of a molded shape.
- the binding matrix should also be relatively inert so that it does not react with the corrosion inhibitors that it is binding.
- the binding matrix of the present invention is chosen such that when combined with the VCI components the resulting blend is in liquid form until cured in a mold. Once cured the resulting product will retain the shape of the mold, and the binding matrix will have permeability characteristics sufficient to allow controlled release of the VCI components.
- the binding matrix can preferably comprise one of several resins, a plastisol, a urethane and an epoxy. Plastisols are dispersions of fine particle size polyvinyl chloride (PVC) or acrylic polymer or copolymer resins in liquid plasticizers which require heat to harden. Organosols may also be used. Organosols are plastisols to which a volatile solvent or thinner has been added.
- Plasticizers work by embedding themselves between the chains of polymers, space them apart (increasing of the “free volume”), and thus significantly lowering the glass transition temperature for the plastic and making it softer.
- Suitable plasticizers for use with PVC are a phthalate, a benzoate, an adipate, or a polymeric plasticizer, etc.
- An acrylic monomer may be used with a plastisol as a cross linking resin to adjust the hardness of the resulting mixture.
- heat or light stabilizers In addition to the resins and plasticizers, heat or light stabilizers, color pigments, flame retardants, blowing agents, fillers, viscosity control agents, rheology control additives or other additives may be included as determined by the intended end use.
- the rate of VCI release from the emitter is controlled by adjusting the components the polymer binding matrix to provide a steady, long lasting rate of emission.
- the mixture is irreversibly converted from a colloidal suspension to a solid solution upon heating so that, unlike a thermoplastic material, repeated heating will not melt the resulting emitter.
- the plastisols are heated to a relatively low temperature range of about 20° C. to 150° C., most preferably about 80° C. to 150° C. after the mixture is poured into a mold. Such relatively low temperatures reduce vaporization of the VCIs in the mixture.
- epoxies and urethanes The same advantageous result can be achieved with epoxies and urethanes. However for these materials, heating of the mixture results in cross linking between two components, again forming an emitter which is irreversibly cured.
- a two component epoxy or urethane comprises an epoxy or urethane and a hardener.
- compositions with preferred ranges which produce a mixture having suitable properties for use as a volatile corrosion inhibitor emitting device.
- Resin plastisols, urethane, epoxy 20–80% (by weight) Plasticizer (for use with plastisols only) 15–35% Cross Linking Resin (for use with plastisols) 0–10% Hardener (for use with epoxy and urethane only) 3–10% Viscosity Control Agent 1–10% Filler 0–30% (10–30% with epoxy and urethane) VCI 10–50%
- Suitable hardeners for urethane include isocyanates and diisocyanates.
- Suitable hardeners for epoxies include amines (diamines, triamines, etc.) and amine adducts.
- Suitable viscosity control agents comprise mineral spirits, texanol diisobutyrate (“TXIB”) and viscosity modifiers from such as BYK Chemie: BYK-3105, BYK-3155, BYK-4040.
- Suitable fillers comprise calcium carbonate, Kaolin Clay and talk (magnesium silicate).
- Other hardeners, viscosity control agents and fillers will be readily apparent to those skilled in the art given the benefit of this disclosure.
- This mixture is particularly suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A corrosion inhibiting mixture is disclosed comprising a volatile corrosion inhibitor and a binding matrix, wherein the binding matrix comprises a resin selected from the group of a plastisol, a urethane and an epoxy. The mixture is liquid near ambient temperature and irreversibly cured when heated in a temperature range of about 20° C. to 150° C.
Description
- This invention relates to improvements in volatile corrosion inhibitors, and more particularly to improvements in volatile corrosion inhibitor delivery devices.
- Corrosion of metal articles is a significant problem. A known technique for reducing the corrosion of metal articles is to package the articles with a material containing a volatile corrosion inhibitor (“VCI”). VCIs function by slowly releasing vapors that contact the surface of the metals. The vapor phase corrosion inhibitors envelop the metal article in a non-corrosive atmosphere and retard moisture and oxygen present in the atmosphere from attacking and reacting with the metal surfaces. Volatile corrosion inhibitors may be applied by spraying the entire surface of the metal article to be protected, or the metal article itself may be enclosed, packaged or surrounded in or with materials containing VCIs. For example, VCIs may be incorporated into a packaging material such as paper and plastic wraps, films, and plastic dunnage. VCIs are also known to be incorporated into an emitting device with a binding matrix. Such emitters can be used within closed spaces such as packaging containers, electrical boxes, storage bags, and other enclosures. Different volatile corrosion inhibitors or combinations of volatile corrosion inhibitors may be selected based on the type of metal to be protected, the size of the enclosure, and the length of time that protection is required.
- Known volatile corrosion inhibitor emitting devices have several drawbacks. They are produced in a set shape such as foam strips, compressed pellets, and air permeable containers such as plastic cups with paper tops. The set shape may not “fit” an intended application. For example, an emitter may be placed randomly in a packaging container or enclosure or stuck to a surface within the package or enclosure. Many end users do not want loose articles or articles that do not appear to be part of the packaging in the containers they receive. Moreover, generic shapes do not adequately identify the function of the VCI device. Since it is sometimes difficult to clearly distinguish that the device is purposely part of the packaging or the enclosure, it may be misplaced or mistakenly removed. Further, there is the problem of reinserting the device as part of a pack and having to locate it properly. Also, some enclosures and packaging do not have surfaces readily available for set shape devices. Moreover, VCI packaging devices produced in this way usually contain the active materials in powder or pellet form. These powders and pellets can spill or spread active materials to unwanted areas. In general known emitter devices have insufficient control over the release of the VCIs.
- U.S. Pat. No. 4,124,549 to Hashiudo et al discloses a method for making a corrosion protective film which includes a thermoplastic resin and a volatile corrosion inhibitor mixed together and molded or extruded. Such a product is disadvantages for several of the reasons cited above. In addition, such a thermoplastic composition would result in the loss of many VCIs at the high temperatures needed to form the film.
- It would be highly desirable to provide a volatile corrosion inhibiting mixture which can be made at relatively low temperatures, which can assume a variety of shapes, and which can provide a controlled release of VCIs.
- In accordance with a first aspect, a corrosion inhibiting mixture is disclosed comprising a volatile corrosion inhibitor and a binding matrix, wherein the binding matrix comprises a resin selected from the group of a plastisol, a urethane and an epoxy. The mixture is liquid near ambient temperature and irreversibly cured when heated in a temperature range of about 20° C. to 150° C.
- From the foregoing disclosure and the following more detailed description of various preferred embodiments it will be apparent to those skilled in the art that the present invention provides a significant advance in the technology of volatile corrosion inhibitors. Particularly significant in this regard is the potential the invention affords for providing a high quality, low cost volatile corrosion inhibitor delivery technique. Additional features and advantages of various preferred embodiments will be better understood in view of the detailed description provided below.
- It will be apparent to those skilled in the art, that is, to those who have knowledge or experience in this area of technology, that many uses and design variations are possible for the volatile corrosion inhibiting device disclosed here. The following detailed discussion of various alternative and preferred features and embodiments will illustrate the general principles of the invention with reference to a volatile corrosion inhibiting device suitable for use in an application where it is desired to protect metal. Other embodiments suitable for other applications will be apparent to those skilled in the art given the benefit of this disclosure.
- In accordance with a preferred embodiment, a vapor-phase or volatile corrosion inhibitor emitting device comprises a volatile corrosion inhibitor and a binding matrix. This mixture is combined to form a pourable and moldable liquid at relatively low temperatures, most preferably ambient room temperature (about 20° C.). Advantageously, the mixture may be poured into a mold of any desired moldable shape and gently heated to about 20° C. to 150° C. In accordance with a highly advantageous feature, this heating cures the mixture, so that reheating will not result in melting. Also, forming and curing the mixture at low temperatures is advantageous in that loss of volatile corrosion inhibitors is reduced.
- In accordance with a highly advantageous feature, a volatile corrosion inhibitor emitting device is provided which can be readily molded or cast, allowing the emitting device to form a shape that fits a particular application. Many current and potential applications for these devices would be substantially improved if the device could be custom fitted to an enclosure, a packaging container or the items being protected from corrosion. For example, the volatile corrosion inhibitor emitting device can be readily molded or caste into shapes that are known symbols or company logos. With addition of an appropriate pigment, a specific color can be used for a specific application. Emitters may be formed as a narrow cylinder to protect gun barrels, fish-shaped to protect tackle boxes, a bolt to protect tool boxes, a blue shield to protect ferrous based metals, a red shield to protect electrical boxes, etc.
- Different corrosion inhibitors or combinations of corrosion inhibitors are selected based on the type of metal to be protected, the size of the enclosure, and the length of time that protection is required. Examples of VCIs for incorporation into the binding matrix include benzoic acid and inorganic salts of benzoic acid such as sodium benzoate, inorganic nitrite salts such as sodium nitrite, amine nitrite salts such as dicyclohexylamine nitrite, carboxylic acids such as caprylic acid, salts of amines and carboxylic acids such as cyclohexylamine benzoate, monoethanolamine benzoate, diethylethanolamine caprylate, and diethylethanolamine caprate, azoles such as tolyltriazole, benzotriazole and their salts, and salts of molybdenum such as sodium molybdate or an amine molybdate. Other volatile corrosion inhibitors suitable for use herein will be readily apparent to those skilled in the art given the benefit of this disclosure.
- The binding matrix preferably satisfies a number of conditions. It should be processable at temperatures low enough that the volatile corrosion inhibitors are not driven off during processing. The binding matrix should be able to be readily adjusted to control the emission rate of the volatile corrosion inhibitors. It should be capable of being readily molded or cast into various shapes. The binding matrix should have long term durability for extended use applications. It should be permeable enough to allow the corrosion inhibitor(s) to migrate out of a molded shape. The binding matrix should also be relatively inert so that it does not react with the corrosion inhibitors that it is binding.
- The binding matrix of the present invention is chosen such that when combined with the VCI components the resulting blend is in liquid form until cured in a mold. Once cured the resulting product will retain the shape of the mold, and the binding matrix will have permeability characteristics sufficient to allow controlled release of the VCI components. The binding matrix can preferably comprise one of several resins, a plastisol, a urethane and an epoxy. Plastisols are dispersions of fine particle size polyvinyl chloride (PVC) or acrylic polymer or copolymer resins in liquid plasticizers which require heat to harden. Organosols may also be used. Organosols are plastisols to which a volatile solvent or thinner has been added. Plastisols typically require a plasticizer, an additive which softens the mixture to which it is are added. Plasticizers work by embedding themselves between the chains of polymers, space them apart (increasing of the “free volume”), and thus significantly lowering the glass transition temperature for the plastic and making it softer. Suitable plasticizers for use with PVC are a phthalate, a benzoate, an adipate, or a polymeric plasticizer, etc. An acrylic monomer may be used with a plastisol as a cross linking resin to adjust the hardness of the resulting mixture.
- In addition to the resins and plasticizers, heat or light stabilizers, color pigments, flame retardants, blowing agents, fillers, viscosity control agents, rheology control additives or other additives may be included as determined by the intended end use. The rate of VCI release from the emitter is controlled by adjusting the components the polymer binding matrix to provide a steady, long lasting rate of emission.
- With plastisols, the mixture is irreversibly converted from a colloidal suspension to a solid solution upon heating so that, unlike a thermoplastic material, repeated heating will not melt the resulting emitter. Advantageously, the plastisols are heated to a relatively low temperature range of about 20° C. to 150° C., most preferably about 80° C. to 150° C. after the mixture is poured into a mold. Such relatively low temperatures reduce vaporization of the VCIs in the mixture. The same advantageous result can be achieved with epoxies and urethanes. However for these materials, heating of the mixture results in cross linking between two components, again forming an emitter which is irreversibly cured. A two component epoxy or urethane comprises an epoxy or urethane and a hardener.
- Listed below is a summary of several compositions with preferred ranges which produce a mixture having suitable properties for use as a volatile corrosion inhibitor emitting device.
-
Resin (plastisols, urethane, epoxy) 20–80% (by weight) Plasticizer (for use with plastisols only) 15–35% Cross Linking Resin (for use with plastisols) 0–10% Hardener (for use with epoxy and urethane only) 3–10% Viscosity Control Agent 1–10% Filler 0–30% (10–30% with epoxy and urethane) VCI 10–50% - Suitable hardeners for urethane include isocyanates and diisocyanates. Suitable hardeners for epoxies include amines (diamines, triamines, etc.) and amine adducts. Suitable viscosity control agents comprise mineral spirits, texanol diisobutyrate (“TXIB”) and viscosity modifiers from such as BYK Chemie: BYK-3105, BYK-3155, BYK-4040. Suitable fillers comprise calcium carbonate, Kaolin Clay and talk (magnesium silicate). Other hardeners, viscosity control agents and fillers will be readily apparent to those skilled in the art given the benefit of this disclosure.
- The invention disclosed here will be better understood with the aid of the following non-limiting examples of certain preferred embodiments.
- This mixture is particularly suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- 50% Formolon 40 PVC by Formosa Plastics
- 16% Plasticizer:
-
- 8% dibutylphthalate (DBP)
- 8% Santicizer 278 Benzoate by Ferro Corp.
- 1% Viscosity Control Agent: BYK-3155 from BYK Chemie
- 10% Calcium Carbonate
- 23% VCIs:
-
- 10% caprylic acid
- 7% diethyl ethanol amine
- 6% benzotriazole
- Mix the components together at ambient conditions to form a liquid mixture. Pour the liquid mixture into a mold. Heat the mold to about 110° C. to irreversibly cure the mixture and form VCI emitter devices.
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- 40% DEGALAN® PAMA powder resin by Rohm GmbH
- 20% Plasticizer:
-
- 10% dihexylphthalate (DHP)
- 10% Santicizer 278 Benzoate by Ferro Corp.
- 1% Viscosity Control Agent: BYK-4040 from BYK Chemie
- 15% Calcium Carbonate
- 24% VCIs:
-
- 9% Benzoic acid
- 9% cyclohexylamine
- 6% benzotriazole
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- 60% Desmodur 1150 Polyesterether Polyol by Bayer
- 6% Isocyanate hardener
- 1% Viscosity Control Agent: BYK-3155 from BYK Chemie
- 5% Calcium Carbonate
- 28% VCIs:
-
- 10% Sodium benzoate
- 10% Ammonium benzoate
- 8% Tolytriazole
- This mixture is also suitable for use as a corrosion inhibitor for ferrous and multi-metal materials.
- 60% RENCAST 3209 epoxy resin from Huntsman
- 6% REN 3209 hardener from Huntsman
- 1% Viscosity Control Agent: BYK-3155 from BYK Chemie
- 5% Calcium Carbonate
- 28% VCIs:
-
- 10% carpylic acid
- 7% diethyl ethanolamine
- 6% benzotriazole
- From the foregoing disclosure and detailed description of certain preferred embodiments, it will be apparent that various modifications, additions and other alternative embodiments are possible without departing from the true scope and spirit of the invention. The embodiments discussed were chosen and described to provide the best illustration of the principles of the invention and its practical application to thereby enable one of ordinary skill in the art to use the invention in various embodiments and with various modifications as are suited to the particular use contemplated. All such modifications and variations are within the scope of the invention as determined by the appended claims when interpreted in accordance with the breadth to which they are fairly, legally, and equitably entitled.
Claims (9)
1. A corrosion inhibiting mixture comprising, in combination:
a volatile corrosion inhibitor; and
a binding matrix, wherein the binding matrix comprises a resin selected from the group of a plastisol, a urethane and an epoxy;
wherein the mixture is liquid near ambient temperature and irreversibly cured when heated in a temperature range of about 20° C. to 150° C.
2. The corrosion inhibiting mixture of claim 1 wherein the volatile corrosion inhibitor is selected from the group consisting of at least one of benzoic acid, a salt of benzoic acid, an inorganic nitrite salt, an amine nitrite salt, a carboxylic acid, a salt of a carboxylic acid, a salt of an amine, an azole, a salt of an azole, a salt of molybdenum and an amine molybdates.
3. The corrosion inhibiting mixture of claim 1 wherein the volatile corrosion inhibitor comprises about 10-50% by weight of the mixture, and the binding matrix comprises about 90-50% by weight of the mixture.
4. The corrosion inhibiting mixture of claim 1 wherein the binding matrix comprises a plastisol formed from a plasticizer and one of a PVC resin and an acrylic co-polymer.
5. The corrosion inhibiting mixture of claim 4 wherein the plastisol is a PVC resin which comprises about 20-60% by weight of the mixture, and the plasticizer comprises about 15-35% by weight of the mixture.
6. The corrosion inhibiting mixture of claim 4 wherein the plastisol is an acrylic copolymer and the resin further comprises a cross linking resin.
7. The corrosion inhibiting mixture of claim 1 further comprising about 1-10% by weight of a viscosity control agent.
8. The corrosion inhibiting mixture of claim 1 further comprising about 1-30% by weight of a mineral filler.
9. The corrosion inhibiting mixture of claim 1 wherein the binding matrix comprises about 3-10% by weight of a hardener and the resin comprises about 50-85% by weight of one of a urethane and an epoxy.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/588,885 US20080099729A1 (en) | 2006-10-27 | 2006-10-27 | Corrosion inhibiting mixture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/588,885 US20080099729A1 (en) | 2006-10-27 | 2006-10-27 | Corrosion inhibiting mixture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20080099729A1 true US20080099729A1 (en) | 2008-05-01 |
Family
ID=39329022
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/588,885 Abandoned US20080099729A1 (en) | 2006-10-27 | 2006-10-27 | Corrosion inhibiting mixture |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US20080099729A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090111901A1 (en) * | 2007-10-29 | 2009-04-30 | Allen William M | Corrosion Inhibiting Protective Foam Packaging |
Citations (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3443577A (en) * | 1965-10-21 | 1969-05-13 | Alfa Laval Ab | Apparatus for controlling gravity flow |
| US3836077A (en) * | 1971-06-03 | 1974-09-17 | J Skildum | Apparatus protector |
| US3936560A (en) * | 1974-02-22 | 1976-02-03 | The Orchard Corporation Of America | Self-sealable corrosion protectable packaging material and method of making |
| US3967926A (en) * | 1973-11-09 | 1976-07-06 | Iosif Lvovich Rozenfeld | Method for inhibiting the corrosion of metals with vapor phase inhibitors disposed in a zeolite carrier |
| US3969127A (en) * | 1972-07-07 | 1976-07-13 | The Sherwin-Williams Company | Molybdate corrosion inhibiting pigment and method for preparing same |
| US4051066A (en) * | 1975-01-13 | 1977-09-27 | Northern Instruments Corporation | Corrosion-inhibiting rubber and methods of preparation |
| US4124549A (en) * | 1974-08-22 | 1978-11-07 | Aicello Chemical Co., Ltd. | Corrosion-inhibiting plastic films |
| US4127562A (en) * | 1974-09-12 | 1978-11-28 | Veba-Chemie Aktiengesellschaft | Method of preparing coatings |
| US4210567A (en) * | 1974-11-15 | 1980-07-01 | Teroson G.M.B.H. | Plastisol of an acrylate polymer and a plasticizer |
| US4275835A (en) * | 1979-05-07 | 1981-06-30 | Miksic Boris A | Corrosion inhibiting articles |
| US4290912A (en) * | 1980-02-21 | 1981-09-22 | Northern Instruments Corporation | Volatile corrosion inhibiting article |
| US4338209A (en) * | 1977-10-01 | 1982-07-06 | Otsuka Chemical Co., Ltd. | Metal corrosion inhibitor |
| US4349457A (en) * | 1980-03-10 | 1982-09-14 | The Dow Chemical Co. | Corrosion protection for metal surfaces |
| US4402747A (en) * | 1981-05-15 | 1983-09-06 | United States Steel Corporation | Rust Inhibiting for steel |
| US4416701A (en) * | 1981-03-18 | 1983-11-22 | Westfalia Separator Ag | Method of producing starch from grain or ground grain products by the wet process |
| US4454266A (en) * | 1983-04-11 | 1984-06-12 | Daubert Coated Products Inc. | Release coating compositions |
| US4557966A (en) * | 1984-04-06 | 1985-12-10 | The Cromwell Paper Company | Ferrous metal corrosion inhibiting sheet material |
| US4623558A (en) * | 1985-05-29 | 1986-11-18 | W. R. Grace & Co. | Reactive plastisol dispersion |
| US4913874A (en) * | 1989-02-21 | 1990-04-03 | Pinchuk Leonid S | Process of providing tubular polymeric anticorrosion film |
| US4963290A (en) * | 1988-02-18 | 1990-10-16 | Gaz De France (Service National) | Corrosion inhibitors of steels and aqueous compositions of alkali meal halide containing them |
| US4973448A (en) * | 1986-11-18 | 1990-11-27 | Cortec Corporation | Vapor phase corrosion inhibitor product and method containing a desiccant |
| US5209869A (en) * | 1988-08-23 | 1993-05-11 | Cortec Corporation | Vapor phase corrosion inhibitor-dessiccant material |
| US5303743A (en) * | 1991-05-08 | 1994-04-19 | Vincent Larry W | Thread protection system |
| US5320778A (en) * | 1988-08-23 | 1994-06-14 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5332525A (en) * | 1988-08-23 | 1994-07-26 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5344589A (en) * | 1988-08-23 | 1994-09-06 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5455075A (en) * | 1994-03-10 | 1995-10-03 | Daubert Chemical Company, Inc. | Hot melt corrosion inhibiting coating composition |
| US5677053A (en) * | 1995-06-29 | 1997-10-14 | Toyo Seikan Kaisha, Ltd. | Acrylic plastisol adhesion structure |
| US5744565A (en) * | 1995-11-16 | 1998-04-28 | Roehm Gmbh Chemische Fabrik | Plastisols |
| US5888281A (en) * | 1997-08-22 | 1999-03-30 | Daubert Chemical Company, Inc. | Corrosion inhibiting composition |
| US5958115A (en) * | 1997-02-28 | 1999-09-28 | EXCOR Korrosionsschutz-Technolgien und--Produkte GmbH | Corrosion-inhibiting composite material |
| US5965645A (en) * | 1993-05-07 | 1999-10-12 | Teroson Gmbh | Plastisol composition |
| US6033599A (en) * | 1998-10-13 | 2000-03-07 | Interwrap Industries Inc. | Vapor phase corrosion inhibitors |
| US6124044A (en) * | 1995-10-27 | 2000-09-26 | Cal-West Equipment Company, Inc. | Polymeric peel-off coating compositions and methods of use thereof |
| US6432485B1 (en) * | 1998-09-24 | 2002-08-13 | E. I. Dupont De Nemours & Company | Epoxide/amine based aqueous coating agents and use thereof in multicoat lacquers |
| US20030213936A1 (en) * | 2002-01-22 | 2003-11-20 | Northern Technologies International Corporation | Corrosion inhibiting formula and corrosion inhibiting articles using same |
| US6787065B1 (en) * | 1998-02-17 | 2004-09-07 | Henkel Kgaa | Use of a composition or premix based on volatile corrosion inhibitors, composition or premix, articles comprising said composition and preparation method |
-
2006
- 2006-10-27 US US11/588,885 patent/US20080099729A1/en not_active Abandoned
Patent Citations (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3443577A (en) * | 1965-10-21 | 1969-05-13 | Alfa Laval Ab | Apparatus for controlling gravity flow |
| US3836077A (en) * | 1971-06-03 | 1974-09-17 | J Skildum | Apparatus protector |
| US3969127A (en) * | 1972-07-07 | 1976-07-13 | The Sherwin-Williams Company | Molybdate corrosion inhibiting pigment and method for preparing same |
| US3967926A (en) * | 1973-11-09 | 1976-07-06 | Iosif Lvovich Rozenfeld | Method for inhibiting the corrosion of metals with vapor phase inhibitors disposed in a zeolite carrier |
| US3936560A (en) * | 1974-02-22 | 1976-02-03 | The Orchard Corporation Of America | Self-sealable corrosion protectable packaging material and method of making |
| US4124549A (en) * | 1974-08-22 | 1978-11-07 | Aicello Chemical Co., Ltd. | Corrosion-inhibiting plastic films |
| US4127562A (en) * | 1974-09-12 | 1978-11-28 | Veba-Chemie Aktiengesellschaft | Method of preparing coatings |
| US4210567A (en) * | 1974-11-15 | 1980-07-01 | Teroson G.M.B.H. | Plastisol of an acrylate polymer and a plasticizer |
| US4051066A (en) * | 1975-01-13 | 1977-09-27 | Northern Instruments Corporation | Corrosion-inhibiting rubber and methods of preparation |
| US4338209A (en) * | 1977-10-01 | 1982-07-06 | Otsuka Chemical Co., Ltd. | Metal corrosion inhibitor |
| US4275835A (en) * | 1979-05-07 | 1981-06-30 | Miksic Boris A | Corrosion inhibiting articles |
| US4290912A (en) * | 1980-02-21 | 1981-09-22 | Northern Instruments Corporation | Volatile corrosion inhibiting article |
| US4349457A (en) * | 1980-03-10 | 1982-09-14 | The Dow Chemical Co. | Corrosion protection for metal surfaces |
| US4416701A (en) * | 1981-03-18 | 1983-11-22 | Westfalia Separator Ag | Method of producing starch from grain or ground grain products by the wet process |
| US4402747A (en) * | 1981-05-15 | 1983-09-06 | United States Steel Corporation | Rust Inhibiting for steel |
| US4454266A (en) * | 1983-04-11 | 1984-06-12 | Daubert Coated Products Inc. | Release coating compositions |
| US4557966A (en) * | 1984-04-06 | 1985-12-10 | The Cromwell Paper Company | Ferrous metal corrosion inhibiting sheet material |
| US4623558A (en) * | 1985-05-29 | 1986-11-18 | W. R. Grace & Co. | Reactive plastisol dispersion |
| US4973448A (en) * | 1986-11-18 | 1990-11-27 | Cortec Corporation | Vapor phase corrosion inhibitor product and method containing a desiccant |
| US4963290A (en) * | 1988-02-18 | 1990-10-16 | Gaz De France (Service National) | Corrosion inhibitors of steels and aqueous compositions of alkali meal halide containing them |
| US5422187A (en) * | 1988-08-23 | 1995-06-06 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5209869A (en) * | 1988-08-23 | 1993-05-11 | Cortec Corporation | Vapor phase corrosion inhibitor-dessiccant material |
| US5320778A (en) * | 1988-08-23 | 1994-06-14 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5332525A (en) * | 1988-08-23 | 1994-07-26 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5344589A (en) * | 1988-08-23 | 1994-09-06 | Cortec Corporation | Vapor phase corrosion inhibitor-desiccant material |
| US5393457A (en) * | 1988-08-23 | 1995-02-28 | Miksic; Boris A. | Vapor phase corrosion inhibitor-desiccant material |
| US4913874A (en) * | 1989-02-21 | 1990-04-03 | Pinchuk Leonid S | Process of providing tubular polymeric anticorrosion film |
| US5303743A (en) * | 1991-05-08 | 1994-04-19 | Vincent Larry W | Thread protection system |
| US5965645A (en) * | 1993-05-07 | 1999-10-12 | Teroson Gmbh | Plastisol composition |
| US5455075A (en) * | 1994-03-10 | 1995-10-03 | Daubert Chemical Company, Inc. | Hot melt corrosion inhibiting coating composition |
| US5677053A (en) * | 1995-06-29 | 1997-10-14 | Toyo Seikan Kaisha, Ltd. | Acrylic plastisol adhesion structure |
| US6124044A (en) * | 1995-10-27 | 2000-09-26 | Cal-West Equipment Company, Inc. | Polymeric peel-off coating compositions and methods of use thereof |
| US5744565A (en) * | 1995-11-16 | 1998-04-28 | Roehm Gmbh Chemische Fabrik | Plastisols |
| US5958115A (en) * | 1997-02-28 | 1999-09-28 | EXCOR Korrosionsschutz-Technolgien und--Produkte GmbH | Corrosion-inhibiting composite material |
| US5888281A (en) * | 1997-08-22 | 1999-03-30 | Daubert Chemical Company, Inc. | Corrosion inhibiting composition |
| US6787065B1 (en) * | 1998-02-17 | 2004-09-07 | Henkel Kgaa | Use of a composition or premix based on volatile corrosion inhibitors, composition or premix, articles comprising said composition and preparation method |
| US6432485B1 (en) * | 1998-09-24 | 2002-08-13 | E. I. Dupont De Nemours & Company | Epoxide/amine based aqueous coating agents and use thereof in multicoat lacquers |
| US6033599A (en) * | 1998-10-13 | 2000-03-07 | Interwrap Industries Inc. | Vapor phase corrosion inhibitors |
| US20030213936A1 (en) * | 2002-01-22 | 2003-11-20 | Northern Technologies International Corporation | Corrosion inhibiting formula and corrosion inhibiting articles using same |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090111901A1 (en) * | 2007-10-29 | 2009-04-30 | Allen William M | Corrosion Inhibiting Protective Foam Packaging |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2298327C (en) | Biodegradable products comprising a vapor phase corrosion inhibitor | |
| EP0990676B1 (en) | Biodegradable vapor corrosion inhibitor products | |
| Flick | Plastics Additives, Volume 1: An Industry Guide | |
| US4124549A (en) | Corrosion-inhibiting plastic films | |
| US6787065B1 (en) | Use of a composition or premix based on volatile corrosion inhibitors, composition or premix, articles comprising said composition and preparation method | |
| CN1267323C (en) | Producing method for plastic shipping and storage containers and composition | |
| EP1641960B1 (en) | Corrosion inhibiting composition and article containing it | |
| KR101099955B1 (en) | HBN-Rubber as crosslinking agent | |
| US6054512A (en) | Corrosion inhibiting thermoplastic alloys | |
| JP7337593B2 (en) | Pellets, melt-molded products made from the same, and methods for producing the same | |
| US7485177B1 (en) | Volatile corrosion inhibiting mixture with tracing agent | |
| TW201546170A (en) | Elastomeric composition having oil resistance | |
| US20030213936A1 (en) | Corrosion inhibiting formula and corrosion inhibiting articles using same | |
| AU605513B2 (en) | An agent for imparting antistatic characteristics to a thermoplastic polymer and a thermoplastic polymer composition containing the agent. | |
| US20080099729A1 (en) | Corrosion inhibiting mixture | |
| US6555600B2 (en) | Corrosion inhibiting thermoplastic alloys | |
| US20030207974A1 (en) | Tarnish inhibiting formula and tarnish inhibiting articles using same | |
| KR102119157B1 (en) | Coating Composition for Iron and Concrete Structure and Construction Methods Using Thereof | |
| US20080069989A1 (en) | Rust-inhibiting injection molded objects | |
| EP3233962B1 (en) | Antistatic polymers and methods of making the same | |
| JP2005120124A (en) | Ethylene-acrylic rubber composition | |
| US5229428A (en) | Closure assembly and method of making same using epoxidized natural oil in a low fusing, curable plastisol | |
| US11781067B2 (en) | Compositions and methods for releasing vapor phase corrosion inhibitors | |
| JP5030543B2 (en) | Acrylic plastisol composition for gloves | |
| JP4607544B2 (en) | Two-part sealer composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: SKS INDUSTRIES, INC., MICHIGAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MCCONNELL, ROBIN;REEL/FRAME:018476/0301 Effective date: 20061027 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |