JPH07232907A - Zinc phosphite strontium based pigment and coating material containing the same - Google Patents
Zinc phosphite strontium based pigment and coating material containing the sameInfo
- Publication number
- JPH07232907A JPH07232907A JP6197994A JP6197994A JPH07232907A JP H07232907 A JPH07232907 A JP H07232907A JP 6197994 A JP6197994 A JP 6197994A JP 6197994 A JP6197994 A JP 6197994A JP H07232907 A JPH07232907 A JP H07232907A
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- strontium
- phosphite
- pigment
- compound
- 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.)
- Granted
Links
- 239000000049 pigment Substances 0.000 title claims abstract description 62
- YKJGLGUBQQTOBD-UHFFFAOYSA-N strontium;zinc;phosphite Chemical compound [Zn+2].[Sr+2].[O-]P([O-])[O-] YKJGLGUBQQTOBD-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 239000011248 coating agent Substances 0.000 title description 14
- 238000000576 coating method Methods 0.000 title description 14
- 239000000463 material Substances 0.000 title description 13
- 239000013078 crystal Substances 0.000 claims abstract description 16
- 239000003973 paint Substances 0.000 claims description 23
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
- 229910052742 iron Inorganic materials 0.000 claims description 10
- 229910017052 cobalt Inorganic materials 0.000 claims description 8
- 239000010941 cobalt Substances 0.000 claims description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 7
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- FNDXFUBHPXBGMD-UHFFFAOYSA-N OP(O)O.OP(O)(O)=O Chemical class OP(O)O.OP(O)(O)=O FNDXFUBHPXBGMD-UHFFFAOYSA-N 0.000 claims 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 abstract description 18
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract description 12
- -1 stronitum oxide Chemical compound 0.000 abstract description 10
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 abstract description 9
- 229910000018 strontium carbonate Inorganic materials 0.000 abstract description 9
- 150000003438 strontium compounds Chemical class 0.000 abstract description 8
- 150000003752 zinc compounds Chemical class 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 6
- AUTOISGCBLBLBA-UHFFFAOYSA-N trizinc;diphosphite Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])[O-].[O-]P([O-])[O-] AUTOISGCBLBLBA-UHFFFAOYSA-N 0.000 abstract description 6
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 abstract description 5
- 235000004416 zinc carbonate Nutrition 0.000 abstract description 5
- 239000011667 zinc carbonate Substances 0.000 abstract description 5
- 229910000010 zinc carbonate Inorganic materials 0.000 abstract description 5
- 239000002994 raw material Substances 0.000 abstract description 4
- 239000011787 zinc oxide Substances 0.000 abstract description 4
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 abstract description 3
- 229910001866 strontium hydroxide Inorganic materials 0.000 abstract description 3
- GKTPAOCBXFIJAG-UHFFFAOYSA-N tristrontium;diphosphite Chemical compound [Sr+2].[Sr+2].[Sr+2].[O-]P([O-])[O-].[O-]P([O-])[O-] GKTPAOCBXFIJAG-UHFFFAOYSA-N 0.000 abstract description 2
- 150000003018 phosphorus compounds Chemical class 0.000 abstract 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 28
- 230000003449 preventive effect Effects 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000000843 powder Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 239000012066 reaction slurry Substances 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- VSFBSEDSFCLXNI-UHFFFAOYSA-N calcium;zinc;phosphite Chemical compound [Ca+2].[Zn+2].[O-]P([O-])[O-] VSFBSEDSFCLXNI-UHFFFAOYSA-N 0.000 description 7
- 239000002002 slurry Substances 0.000 description 7
- 235000002639 sodium chloride Nutrition 0.000 description 7
- 239000012065 filter cake Substances 0.000 description 6
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000004898 kneading Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 4
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Chemical class O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002611 lead compounds Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- IDQWCBURUBJWFM-UHFFFAOYSA-N potassium;zinc;phosphite Chemical compound [K+].[Zn+2].[O-]P([O-])[O-] IDQWCBURUBJWFM-UHFFFAOYSA-N 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- XWKBMOUUGHARTI-UHFFFAOYSA-N tricalcium;diphosphite Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])[O-].[O-]P([O-])[O-] XWKBMOUUGHARTI-UHFFFAOYSA-N 0.000 description 2
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 2
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 2
- XAEWLETZEZXLHR-UHFFFAOYSA-N zinc;dioxido(dioxo)molybdenum Chemical compound [Zn+2].[O-][Mo]([O-])(=O)=O XAEWLETZEZXLHR-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- HMTWMTBTWIGXHU-UHFFFAOYSA-N OP([O-])([O-])[O-].[Zn+2].OP([O-])([O-])[O-].[Zn+2].[Zn+2] Chemical compound OP([O-])([O-])[O-].[Zn+2].OP([O-])([O-])[O-].[Zn+2].[Zn+2] HMTWMTBTWIGXHU-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- JLLMWVIABGJKKI-UHFFFAOYSA-N P([O-])([O-])[O-].[Zn+2].[Sr+2].[Zn+2].P([O-])([O-])[O-] Chemical compound P([O-])([O-])[O-].[Zn+2].[Sr+2].[Zn+2].P([O-])([O-])[O-] JLLMWVIABGJKKI-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- YGDKANFNLLMUAQ-UHFFFAOYSA-N [Sr++].OP([O-])[O-] Chemical compound [Sr++].OP([O-])[O-] YGDKANFNLLMUAQ-UHFFFAOYSA-N 0.000 description 1
- YOTAZFFJSGIRTR-UHFFFAOYSA-N [Zn].[P].[Ca] Chemical compound [Zn].[P].[Ca] YOTAZFFJSGIRTR-UHFFFAOYSA-N 0.000 description 1
- VCQAIUIHXQEIHD-UHFFFAOYSA-N [Zn].[Sr] Chemical compound [Zn].[Sr] VCQAIUIHXQEIHD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- HJJOHHHEKFECQI-UHFFFAOYSA-N aluminum;phosphite Chemical compound [Al+3].[O-]P([O-])[O-] HJJOHHHEKFECQI-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000010960 cold rolled steel Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- PMQJYWORJJEMQC-UHFFFAOYSA-N manganese;dihydrate Chemical compound O.O.[Mn] PMQJYWORJJEMQC-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910000159 nickel phosphate Inorganic materials 0.000 description 1
- JOCJYBPHESYFOK-UHFFFAOYSA-K nickel(3+);phosphate Chemical compound [Ni+3].[O-]P([O-])([O-])=O JOCJYBPHESYFOK-UHFFFAOYSA-K 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- UFQXGXDIJMBKTC-UHFFFAOYSA-N oxostrontium Chemical compound [Sr]=O UFQXGXDIJMBKTC-UHFFFAOYSA-N 0.000 description 1
- ZOGYOOUMDVKYLM-UHFFFAOYSA-N phosphane phosphorous acid Chemical compound P.OP(O)O ZOGYOOUMDVKYLM-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- YLQVKIPMXVSQFZ-UHFFFAOYSA-N zinc;hydrogen phosphite Chemical compound [Zn+2].OP([O-])[O-] YLQVKIPMXVSQFZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/04—Compounds of zinc
- C09C1/046—Compounds of zinc containing phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、人体等に対して毒性が
なく、かつ、防錆作用の優れた有する亜りん酸亜鉛スト
ロンチウム系顔料、及び、それを使用した防錆塗料に関
するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a zinc strontium phosphite pigment which is not toxic to the human body and which has an excellent anticorrosion effect, and an anticorrosion paint using the same. .
【0002】[0002]
【従来の技術】従来、防錆顔料として、クロム酸化合
物、鉛化合物が広く使用されてきたが、これらは、優れ
た防錆性を有するにもかかわらず、その中に含まれるク
ロム酸や鉛の毒性が問題になってきた。そのため、無公
害防錆顔料として、クロム酸や鉛を含まない防錆顔料の
開発が進められ、りん酸亜鉛等の金属りん酸塩、トリポ
リりん酸アルミニウム等の縮合りん酸塩、亜りん酸亜
鉛、亜りん酸アルミニウム等の亜りん酸塩、モリブデン
酸亜鉛等のモリブデン酸塩等が検討されてきた。しかし
ながら、これらの化合物はいずれもクロム酸化合物や鉛
化合物に匹敵する防錆性は有していなかった。2. Description of the Related Art Conventionally, chromic acid compounds and lead compounds have been widely used as rust preventive pigments. Toxicity has become a problem. Therefore, as a pollution-free rust preventive pigment, the development of rust preventive pigments that do not contain chromic acid or lead has been promoted, and metal phosphates such as zinc phosphate, condensed phosphates such as aluminum tripolyphosphate, and zinc phosphite. , Phosphites such as aluminum phosphite and molybdates such as zinc molybdate have been investigated. However, none of these compounds has a rust preventive property comparable to that of a chromic acid compound or a lead compound.
【0003】一方、亜りん酸塩系化合物の特性について
種々の検討がなされてきた。特公昭56−9951号公
報には、塩基性亜りん酸亜鉛が、木材表面におけるタン
ニンによる生ずるシミの抑制、かびの発生の防止、及
び、防炎性の付与において有用であることが開示されて
いる。On the other hand, various studies have been made on the characteristics of phosphite compounds. Japanese Examined Patent Publication No. 56-9951 discloses that basic zinc phosphite is useful for suppressing spots caused by tannin on the surface of wood, preventing mold, and imparting flameproofness. There is.
【0004】また、この亜りん酸塩系化合物の防錆性の
向上についても検討されおり、特開昭58−84109
号公報には、亜りん酸カリウム亜鉛が、無公害防錆塗料
として有用であることが開示されており、特開昭58−
194725号公報には、ヒドロキシ亜りん酸亜鉛錯体
が、化学安定性や分散性において、塩基性亜りん酸亜鉛
より優れていることが開示されている。また、特開昭5
9−204663号公報には、塩基性の亜りん酸カリウ
ム亜鉛が、特に無公害防錆塗料として有用であることが
開示されている。Further, improvement of the rust preventive property of this phosphite compound has been studied, and it is disclosed in JP-A-58-84109.
JP-A-58-58 discloses that potassium zinc phosphite is useful as a pollution-free anticorrosive paint.
Japanese Patent No. 194725 discloses that a zinc hydroxyphosphite complex is superior to basic zinc phosphite in chemical stability and dispersibility. In addition, JP-A-5
JP-A 9-204663 discloses that basic potassium zinc phosphite is particularly useful as a pollution-free rust preventive coating material.
【0005】また、本発明者らは、特開平3−1114
57号公報において、亜りん酸亜鉛カルシウムが優れた
防錆性を有することを開示し、特開平3−285808
号公報において、板状結晶の亜りん酸カルシウムが特に
優れた防錆性を有することを開示した。また、特開平5
−339004号公報においても、亜りん酸亜鉛カルシ
ウムが優れた防錆性を有することが開示されている。更
に、前述の特開平3−285808号公報、及び、特開
平6−2169号公報には、亜りん酸亜鉛カルシウム等
のりんのオキシ酸亜鉛カルシウムの製造において、その
コストを下げるために、次亜りん酸ナトリウム製造の際
に副生する亜りん酸カルシウムを利用する方法が開示さ
れている。The inventors of the present invention have also disclosed in Japanese Unexamined Patent Publication No. 3-1114.
JP-A No. 3-285808 discloses that zinc calcium phosphite has excellent rust preventive properties.
In the gazette, it was disclosed that plate-like crystals of calcium phosphite have a particularly excellent rust preventive property. In addition, JP-A-5
Japanese Patent No. 339004 also discloses that zinc calcium phosphite has an excellent rust preventive property. Furthermore, in the above-mentioned JP-A-3-285808 and JP-A-6-2169, in order to reduce the cost in the production of phosphorus calcium zinc oxyate such as zinc calcium phosphite, the following A method of utilizing calcium phosphite produced as a by-product in the production of sodium phosphate is disclosed.
【0006】[0006]
【発明が解決しようとする課題】前述の亜りん酸亜鉛カ
ルシウムに到るまでの無公害顔料は、従来の防錆顔料の
代替として使用するには、塗料安定性が低く、その防錆
性も従来の防錆顔料に比べて低いものであった。そのた
め、新たな安定剤を配合することも必要になり、従来の
防錆顔料と同一の防錆効果をあげるため、顔料や安定剤
の量も多くなり、コストも高いものであった。一方、こ
のような問題を解決すべく発明された亜りん酸亜鉛カル
シウム系顔料よりも更に高い防錆性を有する顔料の出現
も期待されていた。本発明が解決しようとする課題は、
このような期待を実現することにある。The above-mentioned pollution-free pigments up to zinc calcium phosphite have low paint stability and their rust preventive properties when used as a substitute for conventional rust preventive pigments. It was lower than conventional rust preventive pigments. Therefore, it is necessary to add a new stabilizer, and since the same rust preventive effect as that of the conventional rust preventive pigment is obtained, the amount of the pigment and the stabilizer is large and the cost is high. On the other hand, the appearance of a pigment having a higher rust preventive property than that of the zinc calcium phosphite pigment invented to solve such a problem was also expected. The problem to be solved by the present invention is
It is about fulfilling such expectations.
【0007】[0007]
【課題を解決するための手段】本発明者らは、前述の課
題を解決するため、化学式lSr mZn(HPO3)
2・nH2O(ここで、l=0.1〜1、m=0.1〜
1、n=0〜2)で示される亜りん酸亜鉛ストロンチウ
ム結晶からなる顔料に係わる発明(以下「第1発明」と
いう)、亜りん酸亜鉛ストロンチウム50%〜99.9
重量%、および、マンガン、鉄、コバルト、ニッケル、
銅からなる群から選ばれた1種以上の金属の亜りん酸
塩、亜りん酸複塩、りん酸塩、りん酸複塩、酸化物、も
しくは、水酸化物0.1%〜50重量%からなる複合化
合物を含有する亜りん酸亜鉛ストロンチウム系顔料に係
わる発明(以下「第2発明」という)、第1発明に係わ
る亜りん酸亜鉛ストロンチウム結晶からなる顔料を含む
塗料に係わる発明(以下「第3発明」という)、並び
に、第2発明に係わる亜りん酸亜鉛ストロンチウム系顔
料を含有する塗料(以下「第4発明」という)を完成し
た。In order to solve the above-mentioned problems, the inventors of the present invention have the chemical formula 1Sr mZn (HPO 3 ).
2 · nH 2 O (where, l = 0.1 to 1, m = 0.1 to
1, n = 0 to 2), an invention relating to a pigment comprising zinc strontium phosphite crystals (hereinafter referred to as “first invention”), zinc strontium phosphite 50% to 99.9
Wt% and manganese, iron, cobalt, nickel,
0.1% to 50% by weight of phosphite, phosphite double salt, phosphate, phosphate double salt, oxide or hydroxide of one or more metals selected from the group consisting of copper Invention relating to a zinc strontium phosphite-based pigment containing a composite compound consisting of (hereinafter referred to as "second invention"), invention relating to a coating material containing a pigment comprising zinc strontium phosphite crystals according to the first invention (hereinafter " And a coating material containing the zinc strontium phosphite-based pigment according to the second invention (hereinafter referred to as "the fourth invention").
【0008】第1発明に係わる亜りん酸亜鉛ストロンチ
ウム結晶は、一般に化学式lSrmZn(HPO3)2
・nH2O(ここで、l=0.1〜1、m=0.1〜
1、n=0〜2)で示されるものである。そして、l=
m=1の場合は、その粉末X線回折おける面間隔〔d
(Å)〕は6.90,3.75,3.57,3.45,
3.38,3.33,3.24,3.06,3.04,
3.00,2.80,2.61,2.49,2.24の
値を示す。また、このような結晶構造は、l及びmの値
が多少変わっても維持される。The zinc strontium phosphite crystal according to the first aspect of the invention generally has the chemical formula 1SrmZn (HPO 3 ) 2
NH 2 O (where, l = 0.1-1, m = 0.1
1, n = 0 to 2). And l =
When m = 1, the plane spacing [d in the powder X-ray diffraction
(Å)] is 6.90, 3.75, 3.57, 3.45,
3.38, 3.33, 3.24, 3.06, 3.04
The values of 3.00, 2.80, 2.61, 2.49, and 2.24 are shown. Further, such a crystal structure is maintained even if the values of l and m are slightly changed.
【0009】第1発明に係わる亜りん酸亜鉛ストロンチ
ウム結晶からなる顔料は、亜鉛化合物、ストロンチウム
化合物、及び、亜りん酸、もしくは、亜りん酸化合物を
原料として製造される。この亜鉛化合物としては、亜り
ん酸、又は、亜りん酸化合物と反応して亜りん酸亜鉛を
生成するものであれば、どのようなものでもよいが、反
応生成物中に除去困難な異種酸根が残留しないようにす
るために、酸化亜鉛や炭酸亜鉛を使用するのが好まし
い。また、使用されるストロンチウム化合物も、亜りん
酸、又は、亜りん酸化合物と反応して亜りん酸ストロン
チウムを生成するものであれば、どのようなものでもよ
いが、反応生成物中に除去困難な異種酸根が残留しない
ようにするためには、酸化ストロンチウム、炭酸ストロ
ンチウム、又は、水酸化ストロンチウムを使用するのが
好ましい。これらの亜鉛化合物、及び、ストロンチウム
化合物と反応させるのは、亜りん酸、又は、亜りん酸化
合物である。この亜りん酸化合物としては、これらの亜
鉛化合物、及び、ストロンチウム化合物と反応するもの
であれば、どのようなものでもよいが、反応生成物中に
不必要な異種金属や塩基が残留しないようにするため、
亜りん酸、亜りん酸水素亜鉛、亜りん酸水素ストロンチ
ウムを使用するのが好ましい。The pigment composed of zinc strontium phosphite crystals according to the first invention is produced by using a zinc compound, a strontium compound, and phosphorous acid or a phosphorous acid compound as a raw material. The zinc compound may be any one as long as it reacts with phosphorous acid or a phosphorous acid compound to form zinc phosphite, but a different acid radical difficult to remove in the reaction product. It is preferable to use zinc oxide or zinc carbonate in order to prevent the residue from remaining. Also, the strontium compound used may be any one as long as it reacts with phosphorous acid or a phosphorous acid compound to produce strontium phosphite, but it is difficult to remove it in the reaction product. It is preferable to use strontium oxide, strontium carbonate, or strontium hydroxide in order to prevent such different acid radicals from remaining. It is phosphorous acid or a phosphorous acid compound that reacts with these zinc compounds and strontium compounds. As the phosphite compound, any compound may be used so long as it reacts with these zinc compounds and strontium compounds, so that unnecessary foreign metals and bases do not remain in the reaction product. In order to
It is preferable to use phosphorous acid, zinc hydrogen phosphite, or strontium hydrogen phosphite.
【0010】前述の亜鉛化合物、ストロンチウム化合
物、及び、亜りん酸、もしくは、亜りん酸化合物を反応
させる方法としては、湿式反応もしくは乾式反応、又
は、バッチ方式もしくは連続方式等どのような方法でも
よく、また、各原料はどのような順序で添加してもよ
い。湿式反応では、固体の原料は、スラリーとして使用
するが、あらかじめ、ホモジナイザー、ボールミル等
で、強力な剪断処理をして微細なスラリーとして使用す
ることが好ましく、更に、初期反応後、ボールミル、擂
潰機等で混練し反応を完結させることが好ましい。ま
た、乾式反応でも、初期反応後、ボールミル、擂潰機等
で混練し反応を完結させることが好ましい。湿式反応の
反応温度は、室温から90℃までの温度が適しており、
反応時間は通常30分から24時間である。反応終了
後、樹脂に対する分散性や塗料安定性を向上させるため
に、高級脂肪酸やその誘導体、又は、SiO2、Al2
O3等の金属酸化物等で表面処理することができる。例
えば、1〜5重量%のステアリン酸亜鉛を混合しボール
ミルやジェットミル等で混練すればステアリン酸亜鉛で
表面処理した亜りん酸亜鉛ストロンチウムを得ることが
できる。また、けい酸ナトリウム等の可溶性けい酸塩を
添加した後で酸で中和するすることにより、SiO2で
表面処理した亜りん酸亜鉛ストロンチウムを得ることが
できる。このようにして得られた反応スラリーは濾過さ
れ、得られたケーキは乾燥され粉砕される。As the method for reacting the above-mentioned zinc compound, strontium compound and phosphorous acid or phosphorous acid compound, any method such as wet reaction or dry reaction, batch method or continuous method may be used. Moreover, each raw material may be added in any order. In the wet reaction, the solid raw material is used as a slurry, but it is preferable to use a homogenizer, a ball mill or the like in advance to perform a strong shearing treatment to use it as a fine slurry. It is preferable to knead with a machine to complete the reaction. Also in the dry reaction, it is preferable to complete the reaction by kneading with a ball mill, a crusher or the like after the initial reaction. A suitable reaction temperature for the wet reaction is from room temperature to 90 ° C.
The reaction time is usually 30 minutes to 24 hours. After completion of the reaction, in order to improve dispersibility in the resin and coating stability, higher fatty acid or its derivative, or SiO 2 , Al 2
The surface can be treated with a metal oxide such as O 3 . For example, zinc strontium phosphite surface-treated with zinc stearate can be obtained by mixing 1 to 5% by weight of zinc stearate and kneading with a ball mill, jet mill or the like. Further, zinc strontium phosphite surface-treated with SiO 2 can be obtained by neutralizing with an acid after adding a soluble silicate such as sodium silicate. The reaction slurry thus obtained is filtered and the cake obtained is dried and ground.
【0011】このような反応によって得られた生成物に
は、原料の配合比の相違等による未反応の原料や目的と
しない反応生成物が残留することがあるが、例えば、原
料として、酸化亜鉛、炭酸ストロンチウム、及び、亜り
ん酸を使用した場合には、次式に示す範囲内であれば、
得られた亜りん酸亜鉛ストロンチウムの特性や防錆性に
大きな影響を与えない。 ここで、a、b、及び、cは、不等式 a/(b+c)
≧1/6 の関係満たす10以内の整数を表し、l=
0.1〜1、m=0.1〜1、n=0〜2である。The product obtained by such a reaction may remain unreacted starting materials or undesired reaction products due to differences in the mixing ratio of the starting materials. For example, zinc oxide is used as the starting material. , Strontium carbonate, and when using phosphorous acid, if within the range shown in the following formula,
It does not significantly affect the properties and rust resistance of the obtained zinc strontium phosphite. Where a, b, and c are the inequalities a / (b + c)
Represents an integer within 10 that satisfies the relation ≧ 1/6, and l =
0.1-1, m = 0.1-1, and n = 0-2.
【0012】第2発明に係わる複合化合物は、第1発明
に係わる亜りん酸亜鉛ストロンチウム結晶からなる顔料
の製造方法と同様に、酸化亜鉛、炭酸亜鉛等の亜鉛化合
物、及び、酸化ストロンチウム、炭酸ストロンチウム、
水酸化ストロンチウム等のストロンチウム化合物ととも
に、マンガン、鉄、コバルト、ニッケル、及び、銅から
なる群から選ばれた1種以上の金属の酸化物、水酸化物
等の化合物を、亜りん酸、又は、亜りん酸化合物と反応
させても製造されるが、別途に製造された亜りん酸亜鉛
ストロンチウムに、マンガン、鉄、コバルト、ニッケ
ル、及び、銅からなる群から選ばれた1種以上の金属の
亜りん酸塩、亜りん酸複塩、りん酸塩、りん酸複塩等を
添加し、混合してもよい。The composite compound according to the second aspect of the present invention is a zinc compound such as zinc oxide or zinc carbonate, and strontium oxide or strontium carbonate, similar to the method for producing a pigment comprising zinc strontium phosphite crystals according to the first aspect. ,
Along with strontium compounds such as strontium hydroxide, manganese, iron, cobalt, nickel, and compounds such as oxides and hydroxides of one or more metals selected from the group consisting of copper, phosphorous acid, or, It is also produced by reacting with a phosphite compound, but separately produced strontium zinc phosphite is added to one or more metals selected from the group consisting of manganese, iron, cobalt, nickel, and copper. Phosphite, phosphorous acid double salt, phosphoric acid salt, phosphoric acid double salt, etc. may be added and mixed.
【0013】第2発明に係わる複合化合物において、亜
りん酸亜鉛ストロンチウムに、混合されるマンガン、
鉄、コバルト、ニッケル、及び、銅等の化合物の量は、
0.1〜50重量%であることが必要であり、特に0.
2〜20重量%であることが好ましい。0.1重量%未
満であっても、また、50%を超えても、高い防錆性を
有する顔料を得ることができない。In the composite compound according to the second invention, manganese mixed with zinc strontium phosphite,
The amount of compounds such as iron, cobalt, nickel and copper is
It is necessary to be 0.1 to 50% by weight, and in particular, 0.1.
It is preferably from 2 to 20% by weight. If it is less than 0.1% by weight or exceeds 50%, it is impossible to obtain a pigment having a high rust preventive property.
【0014】第3発明に係わる塗料は、第1発明に係わ
る亜りん酸亜鉛ストロンチウム結晶からなる顔料を使用
して塗料化したものであれば、どのようなものでもよ
く、一般に、必要に応じて付加される他の顔料、樹脂、
乾性油、分散剤、溶媒等を含んでいる。The paint according to the third invention may be any paint, as long as it is made into a paint using the pigment comprising the zinc strontium phosphite crystal according to the first invention, and in general, it can be used as needed. Other pigments, resins added,
Contains dry oil, dispersant, solvent, etc.
【0015】第4発明に係わる塗料は、第2発明に係わ
る亜りん酸亜鉛ストロンチウム系顔料を使用して塗料化
したものであれば、どのようなものでもよく、一般に、
必要に応じて付加される他の顔料、樹脂、乾性油、分散
剤、溶媒等を含んでいる。The paint according to the fourth invention may be any paint, as long as it is made into a paint using the zinc strontium phosphite-based pigment according to the second invention.
It contains other pigments, resins, drying oils, dispersants, solvents and the like added as necessary.
【0016】[0016]
【作用】第1発明に係わる亜りん酸亜鉛ストロンチウム
結晶からなる顔料が、どのような作用により、亜りん酸
亜鉛カルシウムより優れた防錆性を有するかは、詳細は
不明であるが、一応、ストロンチウムの標準電極電位が
カルシウムより低く、従って、ストロンチウムのイオン
化傾向がカルシウムより高いため、亜りん酸亜鉛ストロ
ンチウムは、塗膜を透過してきた水に対する溶解度が、
亜りん酸亜鉛カルシウムより高く、より多くの透過水中
の溶存イオンを捕捉でき、更に、母材の鉄の表面に強固
な皮膜を形成するためと考えられる。The function of the pigment comprising zinc strontium phosphite crystals according to the first aspect of the present invention has better anticorrosive properties than that of zinc calcium phosphite, but it is not clear yet. Since the standard electrode potential of strontium is lower than that of calcium, and therefore the ionization tendency of strontium is higher than that of calcium, strontium zinc phosphite has a solubility in water that has permeated the coating film.
It is considered to be higher than zinc calcium phosphite, capable of trapping more dissolved ions in permeated water, and further forming a strong film on the surface of iron of the base material.
【0017】第2発明に係わる亜りん酸亜鉛ストロンチ
ウム系顔料が、どのような作用により、単独の亜りん酸
亜鉛ストロンチウム結晶からなる顔料より優れた防錆性
を有するかは、詳細は不明であるが、一応、マンガン、
鉄、コバルト、ニッケル、銅等の金属化合物は、それ自
身が防錆性を有するだけでなく、特に塗料中の酸化重合
型樹脂の成分の一部と反応して金属石鹸を形成する等、
塗料中の樹脂の硬化触媒として働くと同時に、鉄の表面
に皮膜を形成する際にも触媒として働き、より緻密で強
固な皮膜を形成するためと考えられる。It is not known in detail how the zinc strontium phosphite pigment according to the second aspect of the invention has a superior rust preventive property to the pigment composed of a single zinc strontium phosphite crystal. But for the time being, manganese,
Metal compounds such as iron, cobalt, nickel and copper have not only rust prevention property themselves, but also react with a part of components of the oxidative polymerization type resin in the paint to form metal soap, etc.,
It is considered that it acts not only as a curing catalyst for the resin in the paint but also as a catalyst when forming a film on the surface of iron, thereby forming a denser and stronger film.
【0018】[0018]
1.顔料の製造 〔実施例1〕酸化亜鉛(ZnO)81.4g、炭酸スト
ロンチウム(SrCO3)147.6gを、水1000
mlに分散し、コロイドミルに通し微細化した。このス
ラリーを50℃に加温後、30%亜りん酸溶液547g
を攪拌しながら1時間かけて添加し反応させた。更に、
2時間攪拌後、反応スラリーを濾過し、得られたフィル
ターケーキを110℃で24時間乾燥して粉体(以下
「顔料1」という)を得た。1. Preparation of pigment [Example 1] 81.4 g of zinc oxide (ZnO), 147.6 g of strontium carbonate (SrCO 3 ) and 1000 parts of water.
It was dispersed in ml and passed through a colloid mill to make it fine. After heating this slurry to 50 ° C., 547 g of 30% phosphorous acid solution
Was stirred for 1 hour and reacted. Furthermore,
After stirring for 2 hours, the reaction slurry was filtered, and the obtained filter cake was dried at 110 ° C. for 24 hours to obtain a powder (hereinafter referred to as “pigment 1”).
【0019】〔実施例2〕酸化亜鉛(ZnO)83.3
g、炭酸ストロンチウム(SrCO3)147.6g、
炭酸ニッケル(NiCO3)2.7gを、水1500m
lに分散し、コロイドミルに通し微細化した。このスラ
リーを50℃に加温後、30%亜りん酸溶液560gを
攪拌しながら1時間かけて添加し反応させた。更に、2
時間攪拌後、反応スラリーを濾過し、得られたフィルタ
ーケーキを110℃で24時間乾燥して粉体(以下「顔
料2」という)を得た。Example 2 Zinc oxide (ZnO) 83.3
g, strontium carbonate (SrCO 3 ) 147.6 g,
2.7 g of nickel carbonate (NiCO 3 ) and water 1500 m
1 and dispersed in a colloid mill to make it fine. After heating this slurry to 50 ° C., 560 g of a 30% phosphorous acid solution was added with stirring for 1 hour to cause a reaction. Furthermore, 2
After stirring for an hour, the reaction slurry was filtered, and the obtained filter cake was dried at 110 ° C. for 24 hours to obtain a powder (hereinafter referred to as “pigment 2”).
【0020】〔実施例3〕炭酸亜鉛(ZnCO3)13
2.6g、炭酸ストロンチウム(SrCO3)147.
6g、炭酸ニッケル(NiCO3)6.9gを混合し混
練機に入れ、80%亜りん酸溶液217gを混練しなが
ら1時間かけて添加し反応させた。更に、1時間混練
後、反応生成物300gをアルミナ製ボールミルに移
し、水500mlを加え6時間湿式混練した。その反応
スラリーを濾過し、得られたフィルターケーキを110
℃で24時間乾燥して粉体(以下「顔料3」という)を
得た。Example 3 Zinc carbonate (ZnCO 3 ) 13
2.6 g, strontium carbonate (SrCO 3 ) 147.
6 g and nickel carbonate (NiCO 3 ) 6.9 g were mixed and placed in a kneader, and 217 g of 80% phosphorous acid solution was added and reacted for 1 hour while kneading. Furthermore, after kneading for 1 hour, 300 g of the reaction product was transferred to an alumina ball mill, 500 ml of water was added, and the mixture was wet kneaded for 6 hours. The reaction slurry is filtered and the resulting filter cake is washed with 110
The powder was dried at 24 ° C. for 24 hours to obtain powder (hereinafter referred to as “pigment 3”).
【0021】〔実施例4〕酸化亜鉛(ZnO)83.6
g、酸化ストロンチウム(SrO)103.6g、水酸
化マンガン(Mn(OH)2)2.4gを、水500m
lに分散させスラリーとした。このスラリーを、50℃
に加温した10%亜りん酸溶液1680gに、攪拌しな
がら1時間かけて添加し反せた。更に、1時間攪拌後、
反応スラリーをアルミナ製ボールミルに移し、6時間湿
式混練した。その反応スラリーを濾過し、得られたフィ
ルターケーキを110℃で24時間乾燥して粉体(以下
「顔料4」という)を得た。Example 4 Zinc oxide (ZnO) 83.6
g, strontium oxide (SrO) 103.6 g, manganese hydroxide (Mn (OH) 2 ) 2.4 g, water 500 m
1 to make a slurry. This slurry is heated to 50 ° C.
The mixture was added to 1680 g of a 10% phosphorous acid solution that had been heated to 1 hour with stirring over 1 hour. Furthermore, after stirring for 1 hour,
The reaction slurry was transferred to an alumina ball mill and wet-kneaded for 6 hours. The reaction slurry was filtered, and the obtained filter cake was dried at 110 ° C. for 24 hours to obtain a powder (hereinafter referred to as “pigment 4”).
【0022】〔実施例5〕炭酸亜鉛(ZnCO3)14
2.2g、炭酸ストロンチウム(SrCO3)147.
6g、炭酸マンガン(MnCO3)15.4gを、ホモ
ジナイザーを使用して水1500mlに分散した。1時
間攪拌後、50%亜りん酸溶液372gを攪拌しがら1
時間かけて添加し反応させた。更に、3時間攪拌後、そ
の反応スラリーを濾過し、得られたフィルターケーキを
110℃で24時間乾燥して粉体(以下「顔料5」とい
う)を得た。Example 5 Zinc Carbonate (ZnCO 3 ) 14
2.2 g, strontium carbonate (SrCO 3 ) 147.
6 g and 15.4 g of manganese carbonate (MnCO 3 ) were dispersed in 1500 ml of water using a homogenizer. After stirring for 1 hour, 372 g of a 50% phosphorous acid solution was stirred, and 1
It was added over a period of time and reacted. Furthermore, after stirring for 3 hours, the reaction slurry was filtered, and the obtained filter cake was dried at 110 ° C. for 24 hours to obtain a powder (hereinafter referred to as “pigment 5”).
【0023】〔実施例6〕酸化亜鉛(ZnO)81.4
g、炭酸ストロンチウム(SrCO3)147.6g
を、水1000mlに分散し、コロイドミルに通し微細
化した。このスラリーを50℃に加温後、30%亜りん
酸溶液547gを攪拌しながら1時間かけて添加し反応
させた。更に、2時間攪拌後、反応スラリーを濾過し、
得られたフィルターケーキを110℃で24時間乾燥し
て粉末とした。この粉末95gに、りん酸ニッケル(N
iHPO4)2.5g、及び、りん酸マンガン(MnH
PO4)2.5gを乾式混合して粉体(以下「顔料6」
という)を得た。Example 6 Zinc oxide (ZnO) 81.4
g, strontium carbonate (SrCO 3 ) 147.6 g
Was dispersed in 1000 ml of water and passed through a colloid mill to be finely divided. After heating the slurry to 50 ° C., 547 g of a 30% phosphorous acid solution was added with stirring for 1 hour for reaction. After further stirring for 2 hours, the reaction slurry is filtered,
The filter cake obtained was dried at 110 ° C. for 24 hours to give a powder. To 95 g of this powder, nickel phosphate (N
2.5 g of iHPO 4 and manganese phosphate (MnH
2.5 g of PO 4 was dry mixed to obtain powder (hereinafter referred to as “Pigment 6”).
I got).
【0024】〔比較例〕防錆性等の比較のための顔料と
して、市販のクロム酸亜鉛系(ZPCタイプ)顔料(以
下「顔料7」という)、りん酸亜鉛系顔料(以下「顔料
8」という)、縮合りん酸アルミニウム系顔料(以下
「顔料9」という)、モリブデン酸亜鉛系顔料(以下
「顔料10」という)、及び、タルク(以下「顔料1
1」という)を準備した。[Comparative Example] As pigments for comparison of rust prevention and the like, commercially available zinc chromate pigment (ZPC type) pigment (hereinafter referred to as "Pigment 7"), zinc phosphate pigment (hereinafter referred to as "Pigment 8") , A condensed aluminum phosphate pigment (hereinafter referred to as "Pigment 9"), a zinc molybdate pigment (hereinafter referred to as "Pigment 10"), and talc (hereinafter referred to as "Pigment 1").
1 ”) was prepared.
【0025】2. 水溶性エポキシエステル樹脂系塗料
の製造 実施例1〜6及び比較例で得られた顔料1〜11を、そ
れぞれ、表1の配合比で調整し、ガラスビーズ(Φ1.
5mm)100gと共にサンドミルで1時間分散させて
塗料化し、それぞれ、塗料A1〜A11を得た。なお、
ここで使用した樹脂は、大日本インキ化学工業(株)製
のウォーターゾルCD−540で不揮発分39.2%の
水溶性エポキシエステル樹脂である。顔料1〜11を使
用して塗料A1〜A11を製造する際して特に問題はな
く、また、得られた塗料A1〜A11の安定性において
も特に問題はなかった。2. Production of Water-Soluble Epoxy Ester Resin-Based Paint The pigments 1 to 11 obtained in Examples 1 to 6 and Comparative Example were adjusted with the compounding ratios shown in Table 1, and glass beads (Φ1.
5 mm) and 100 g were dispersed in a sand mill for 1 hour to form coating materials, and coating materials A1 to A11 were obtained. In addition,
The resin used here is Watersol CD-540 manufactured by Dainippon Ink and Chemicals, Inc., which is a water-soluble epoxy ester resin having a nonvolatile content of 39.2%. There were no particular problems in producing coating materials A1 to A11 using pigments 1 to 11, and there were no particular problems in the stability of the obtained coating materials A1 to A11.
【0026】[0026]
【表1】 [Table 1]
【0027】3. 常乾型アクリル樹脂系塗料の製造 実施例1〜6及び比較例で得られた顔料1〜11を、そ
れぞれ、表2の配合比で調整し、ガラスビーズ(Φ1.
5mm)100gと共にサンドミルで1時間分散させて
塗料化し、それぞれ、塗料B1〜B11を得た。なお、
ここで使用した樹脂は、大日本インキ化学工業(株)製
のアクリディックA−126−50で、不揮発分50%
のアクリル樹脂である。顔料1〜11を使用して塗料B
1〜B11を製造する際して特に問題はなく、また、得
られた塗料B1〜B11の安定性においても特に問題は
なかった。3. Manufacture of Acrylic Resin-Based Paints Pigments 1 to 11 obtained in Examples 1 to 6 and Comparative Example were adjusted with the compounding ratios shown in Table 2, and glass beads (Φ1.
5 mm) and 100 g were dispersed in a sand mill for 1 hour to form coating materials, and coating materials B1 to B11 were obtained. In addition,
The resin used here is ACRYDIC A-126-50 manufactured by Dainippon Ink and Chemicals, Inc., with a nonvolatile content of 50%.
It is an acrylic resin. Paint B using Pigments 1-11
There was no particular problem in producing 1 to B11, and there was no particular problem in stability of the obtained coating materials B1 to B11.
【0028】[0028]
【表2】 [Table 2]
【0029】4. 防錆試験 このようにして得られた塗料A1〜11、及び、B1〜
11を、日本テストパネル(株)製の冷間圧延鋼板(J
IS G3142)1.0×70×150mmにバーコ
ーターを用いて1回塗りし、乾燥後の膜厚が30μmに
なるようにした。その後室温で1週間乾燥し、上塗りす
ることなく、スガ試験機(株)製の塩水噴霧式試験機
(ST−ISO−3)を用いて、5%食塩水による塩水
噴霧試験を行い、各塗料の防錆性をテストした。その結
果を表3に示した。表3において、評価の数字は次のよ
うな結果を示す。 1=錆の発生が 100%のもの 2=錆の発生が 75%のもの 3=錆の発生が 50%のもの 4=錆の発生が 25%のもの 5=ふくれや錆の発生がないもの4. Anticorrosion test Paints A1 to 11 and B1 to B1 thus obtained
11 is a cold-rolled steel plate (J
IS G3142) 1.0 × 70 × 150 mm was coated once with a bar coater so that the film thickness after drying was 30 μm. Then, it was dried at room temperature for 1 week, and a salt spray test with 5% saline was conducted using a salt spray tester (ST-ISO-3) manufactured by Suga Test Instruments Co., Ltd. without overcoating, and each paint Was tested for rust resistance. The results are shown in Table 3. In Table 3, the evaluation numbers show the following results. 1 = 100% rust generation 2 = 75% rust generation 3 = 50% rust generation 4 = 25% rust generation 5 = No swelling or rusting
【0030】[0030]
【表3】 [Table 3]
【0031】表3に示されるように、本発明に係わる亜
りん酸亜鉛ストロンチウム結晶からなる顔料を含む塗料
は、市販のクロム酸亜鉛系顔料を含む塗料と同等以上の
防錆性を有しており、更に、本発明に係わる亜りん酸亜
鉛ストロンチウムと、マンガン、鉄、コバルト、ニッケ
ル等からなる群から選ばれた1種以上の金属の亜りん酸
塩、りん酸塩等とからなる亜りん酸亜鉛ストロンチウム
系顔料を含む塗料は、更に優れた防錆性を有しているこ
とがわかる。As shown in Table 3, the paint containing the pigment comprising zinc strontium zinc phosphite crystals according to the present invention has the same or more rust preventive properties as the paint containing the commercially available zinc chromate pigment. Further, phosphorus phosphite comprising strontium zinc phosphite according to the present invention and phosphite, phosphate, etc. of one or more metals selected from the group consisting of manganese, iron, cobalt, nickel and the like. It can be seen that the coating material containing the zinc strontium acid pigment has more excellent rust prevention.
【0032】[0032]
【発明の効果】本発明に係わる亜りん酸亜鉛ストロンチ
ウム結晶からなる顔料、亜りん酸亜鉛ストロンチウム
と、マンガン、鉄、コバルト、ニッケル、及び、銅から
なる群から選ばれた1種以上の金属の亜りん酸塩、りん
酸塩等とからなる亜りん酸亜鉛ストロンチウム系顔料、
並びに、これらの顔料を含む塗料は、前述のような構成
と作用を有するので、無公害、低毒性であり、優れた防
錆性と塗料安定性を有するので、食器、玩具、船底等の
塗料として、安心して使用することができる。The pigment according to the present invention comprising zinc strontium phosphite crystals, zinc strontium phosphite and one or more metals selected from the group consisting of manganese, iron, cobalt, nickel and copper. Zinc strontium phosphite pigment consisting of phosphite, phosphate, etc.,
In addition, the paint containing these pigments has no pollution and low toxicity because it has the above-mentioned constitution and action, and has excellent rust preventive property and paint stability. Therefore, it is a paint for tableware, toys, ship bottoms, etc. As you can use it with confidence.
Claims (4)
ロンチウム結晶からなる顔料 lSr mZn(HPO3)2・nH2O………………………………(1) (ここで、l=0.1〜1、m=0.1〜1、n=0〜
2)1. A pigment comprising a strontium zinc phosphite crystal represented by the following formula (1): 1Sr mZn (HPO 3 ) 2 .nH 2 O (1) (here) Then, l = 0.1-1, m = 0.1-1, n = 0
2)
9.9重量%、並びに、マンガン、鉄、コバルト、ニッ
ケル、及び、銅からなる群から選ばれた1種以上の金属
の亜りん酸塩、亜りん酸複塩、りん酸塩、りん酸複塩、
酸化物、もしくは、水酸化物0.1%〜50重量%から
なる複合化合物を含有する亜りん酸亜鉛ストロンチウム
系顔料2. Strontium zinc phosphite 50% to 9
9.9% by weight, and phosphites, phosphites double salts, phosphites and phosphate phosphites of one or more metals selected from the group consisting of manganese, iron, cobalt, nickel and copper. salt,
Zinc strontium phosphite-based pigment containing a complex compound of oxide or hydroxide 0.1% to 50% by weight
ロンチウム結晶からなる顔料を含む塗料3. A paint containing a pigment comprising the zinc strontium phosphite crystal according to claim 1.
ロンチウム系顔料を含有する塗料4. A paint containing the zinc strontium phosphite pigment according to claim 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP06197994A JP3513774B2 (en) | 1994-02-21 | 1994-02-21 | Zinc strontium phosphite anticorrosive paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP06197994A JP3513774B2 (en) | 1994-02-21 | 1994-02-21 | Zinc strontium phosphite anticorrosive paint |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH07232907A true JPH07232907A (en) | 1995-09-05 |
| JP3513774B2 JP3513774B2 (en) | 2004-03-31 |
Family
ID=13186814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP06197994A Expired - Fee Related JP3513774B2 (en) | 1994-02-21 | 1994-02-21 | Zinc strontium phosphite anticorrosive paint |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3513774B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006089584A (en) * | 2004-09-24 | 2006-04-06 | Nippon Kouatsu Electric Co | Grounding resistance reducing material and its construction method |
| CN106590034B (en) * | 2016-12-13 | 2019-01-01 | 广西壮族自治区化工研究院 | A kind of phosphite powder of nano-oxide inorganic coating and water paint containing the powder |
-
1994
- 1994-02-21 JP JP06197994A patent/JP3513774B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006089584A (en) * | 2004-09-24 | 2006-04-06 | Nippon Kouatsu Electric Co | Grounding resistance reducing material and its construction method |
| CN106590034B (en) * | 2016-12-13 | 2019-01-01 | 广西壮族自治区化工研究院 | A kind of phosphite powder of nano-oxide inorganic coating and water paint containing the powder |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3513774B2 (en) | 2004-03-31 |
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