JPS6014971A - Powder coating method of reinforcing bar - Google Patents
Powder coating method of reinforcing barInfo
- Publication number
- JPS6014971A JPS6014971A JP12146883A JP12146883A JPS6014971A JP S6014971 A JPS6014971 A JP S6014971A JP 12146883 A JP12146883 A JP 12146883A JP 12146883 A JP12146883 A JP 12146883A JP S6014971 A JPS6014971 A JP S6014971A
- Authority
- JP
- Japan
- Prior art keywords
- powder coating
- reinforcing bar
- coating
- powder
- melting point
- 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
- 238000000576 coating method Methods 0.000 title claims description 68
- 239000000843 powder Substances 0.000 title claims description 54
- 230000003014 reinforcing effect Effects 0.000 title claims description 33
- 239000011248 coating agent Substances 0.000 claims description 58
- 238000002844 melting Methods 0.000 claims description 20
- 230000008018 melting Effects 0.000 claims description 20
- 239000003822 epoxy resin Substances 0.000 claims description 16
- 229920000647 polyepoxide Polymers 0.000 claims description 16
- 239000008199 coating composition Substances 0.000 claims description 14
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 14
- 229920002732 Polyanhydride Polymers 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 125000003700 epoxy group Chemical group 0.000 claims description 4
- 239000010408 film Substances 0.000 description 29
- 230000007797 corrosion Effects 0.000 description 11
- 238000005260 corrosion Methods 0.000 description 11
- 238000005452 bending Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000003973 paint Substances 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 229940098458 powder spray Drugs 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000001723 curing Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000005856 abnormality Effects 0.000 description 3
- 238000005422 blasting Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- -1 chlorine ions Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- RPGWZZNNEUHDAQ-UHFFFAOYSA-N phenylphosphine Chemical compound PC1=CC=CC=C1 RPGWZZNNEUHDAQ-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241001239379 Calophysus macropterus Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910001294 Reinforcing steel Inorganic materials 0.000 description 1
- 241001178076 Zaga Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000013035 low temperature curing Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
あるO
一般にコンク.リート構造物においては、強度を持たせ
るため、通常鉄筋棒、特に、外周部に凸部を有する異形
鉄筋棒が挿入されている。従来、この鉄筋棒はコンクリ
ートがアルカリ性環境となっているため、その表面に不
働態皮膜と呼ばれる水和酸化物の薄い皮膜が形成され、
それ故鉄筋棒の腐食は、殆ど問題にならなかった。DETAILED DESCRIPTION OF THE INVENTION A certain O generally contains conc. In REIT structures, reinforcing bars, particularly deformed reinforcing bars having convex portions on the outer periphery, are usually inserted in order to provide strength. Conventionally, this reinforcing bar is made of concrete in an alkaline environment, so a thin film of hydrated oxide called a passive film is formed on the surface.
Corrosion of the reinforcing bars was therefore hardly a problem.
しかしながら近年、骨材資源の涸渇に伴なう海砂の使用
、融氷剤の散布等によシ、コンクリート中の鉄筋棒は、
塩素イオン等の腐食性物質と接触し、前記不働態皮膜が
破壊されたり、あるいは不働態皮膜の形成が阻害され、
その結果鉄筋棒に腐食が生じ問題になってきた。However, in recent years, due to the depletion of aggregate resources, the use of sea sand and the spraying of ice melting agents have made the reinforcing rods in concrete
When it comes into contact with corrosive substances such as chlorine ions, the passive film is destroyed or the formation of the passive film is inhibited,
As a result, corrosion of the reinforcing bars has become a problem.
そこで、鉄筋棒に耐腐食性、耐久性等の優れ之エポキシ
樹脂系粉体塗料を塗装し、腐食から保護する方法が提案
された。Therefore, a method has been proposed in which reinforcing bars are coated with an epoxy resin powder coating that has excellent corrosion resistance and durability to protect them from corrosion.
しかしながら塗装された鉄筋棒は、[し1字型等に変形
して使用されることが多いため、かかる管体塗料として
、耐腐食性だけでなく、前記変形に対し塗膜が変質しな
い程度の曲げ加工性が良好であるものが要求されるが、
従来のエポキシ樹脂系粉体塗料でこれら条件を満たすも
のは未だ知られていない。However, since painted reinforcing rods are often used after being deformed into a shape such as a square, the pipe paint must not only be corrosion resistant, but also be able to withstand the deformation to the extent that the coating film does not deteriorate. Good bending workability is required,
No conventional epoxy resin powder coating that satisfies these conditions is known yet.
本発明者らは、上記の如き現状に鑑み、エポキシ樹脂系
粉体塗料の耐腐食性、耐薬品性等の優れた性能を生かし
つつ、かつ曲げ加工性の優れた塗膜を形成出来、加えて
貯蔵安定性に優れ、低温硬化可能々鉄筋棒用エポキシ樹
脂系粉体塗料につき鋭意検討の結果、本発明に到ったも
のである。In view of the above-mentioned current situation, the present inventors have discovered that they can form a coating film with excellent bending workability while taking advantage of the excellent performance of epoxy resin powder coatings such as corrosion resistance and chemical resistance. The present invention was developed as a result of extensive research into an epoxy resin-based powder coating for reinforcing bars that has excellent storage stability and can be cured at low temperatures.
すなわち本発明は、/gOで以上に予熱した鉄筋棒に
(A)(1) /分子に少なくとも2個以上のエポキシ
基を有し、かつ融点が3θ〜/’10°Cのエピクロル
ヒドリン−ビスフェノール型エポキシ樹脂・・・・・・
・・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・50〜93重量係と(4) 一般式
(但し、m id g〜/gの整数であシ、nはa〜コ
0の整数である)
で示される融点5occ以上のポリ酸ポリ無水物・・・
・・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・・・・・・・・・5−40重量%とからな
る混合物・・・・・・・・・・・・・・・・・・ 70
0重量部と(B))!Jフェニルホスフィン・・・/〜
4=xi部からなる粉体塗料組成物を塗装することを特
徴とする、鉄筋棒の粉体塗装方法に関するものである。That is, the present invention provides (A)(1) epichlorohydrin-bisphenol type having at least two or more epoxy groups in the /molecule and having a melting point of 3θ to /'10°C to a reinforcing bar preheated to /gO or above. Epoxy resin······
・・・・・・・・・・・・・・・・・・・・・・・・
... Polymer with a weight coefficient of 50 to 93 and a melting point of 5 occ or more represented by the general formula (where m id must be an integer of g to /g, and n is an integer of a to 0) Acid polyanhydride...
・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・・・・・・・・・・5-40% by weight・・・・・・・・・・・・・70
0 parts by weight and (B))! J phenylphosphine.../~
The present invention relates to a powder coating method for reinforcing steel bars, which is characterized by coating a powder coating composition consisting of 4=xi parts.
本発明で使用する粉体塗料組成物の一成分であるエピク
ロルヒドリン−ビスフェノール型エポキシm脂としては
、エピクロルヒドリン−ビスフェノールA型、エピクロ
ルヒドリン−ビスフェノールF型エポキシ樹脂が使用さ
れるが、7分中に少なくとも2個以上のエポキシ基を持
つものが適当である。エポキシ基の数が少なくなると塗
膜強度、密着性等が低下するので好ましくない。As the epichlorohydrin-bisphenol type epoxy resin which is one component of the powder coating composition used in the present invention, epichlorohydrin-bisphenol A type and epichlorohydrin-bisphenol F type epoxy resin are used. Those having more than 3 epoxy groups are suitable. When the number of epoxy groups decreases, coating film strength, adhesion, etc. decrease, which is not preferable.
またエポキシ樹脂の融点は50〜/4tO°Cが適当で
ある。融点がり0℃未満では、粉体塗料として必須の常
温での粉末状態を維持出来ず、貯蔵安定性が悪くなるの
で好ましくない。逆に/ダθ0Cを越えると、粉体塗料
製造の溶融練合工程では一般に温度を/lθ0C以上と
する必要があることから、低温・速硬化型粉体塗料であ
る本粉体塗料組成物でid溶融練合工程で一部反応が進
行し、これが塗膜性能、特に塗膜の平滑性等に悪影響を
及ばずので好ましくない。Further, the melting point of the epoxy resin is suitably 50 to 4tO°C. If the melting point is less than 0°C, the powder state required for a powder coating at room temperature cannot be maintained and the storage stability becomes poor, which is not preferable. On the other hand, when /daθ0C is exceeded, the temperature must generally be kept above /lθ0C in the melting and kneading process of powder coating production, so this powder coating composition, which is a low-temperature, fast-curing powder coating, Part of the reaction proceeds during the id melt-kneading process, which is not preferable because it does not adversely affect the coating film performance, especially the smoothness of the coating film.
なお、前記のエピクロルヒドリン−ビスフェノール型エ
ポキシ樹脂としては、上記のエポキシ樹脂ヲダイマー酸
、 ポリブタジェン、 アクリロニトリルコ9ム等で変
性したものも使用可能である。As the epichlorohydrin-bisphenol type epoxy resin, the above-mentioned epoxy resins modified with dimer acid, polybutadiene, acrylonitrile, etc. can also be used.
具体的には、市販のエフ3?トートYD−0//、工
号? ト − ト YD−0/、2 、 エ ポ ト
− ト YD−073、エ ポ ト − )YD−77
/l’ 、 エ ポ ト −ト Y D −θ / 7
、 エ ポ ト − ト YDF−2007、工 、
I? ト − ト YDF −コ θ o 4t 、
エ ポ ト − ト YDF−コθθ7(以上東部化成
社製商品名) ; A、E、R。Specifically, commercially available F3? Tote YD-0//, engineering
issue? TOTO YD-0/, 2, EPOTO
- YD-073, epot -) YD-77
/l', epot YD-θ/7
, Epot YDF-2007, Eng.
I? To-to YDF-ko θ o 4t,
EPOTO-TO YDF-KO θθ7 (all trade names manufactured by Tobu Kasei Co., Ltd.); A, E, R.
66/、 A、E、R,A Aケ、 A、E、R,A乙
7(以上旭化成工業社製商品名); エピクロン1oo
o、エピクロン1010、エビクロン301θ、 エビ
クロン30j3−θ(以上大日本インキ化学工業社製商
品名);EPOMIK R−,70/、 EPOMIK
R−、?θコ、EPOMIK R−,301I、EP
OMIK 5R−33、EPOMIK R−3011E
% EPOMIK R−30グP。66/, A, E, R, A
o, Epicron 1010, Ebicuron 301θ, Ebicuron 30j3-θ (all trade names manufactured by Dainippon Ink and Chemicals); EPOMIK R-, 70/, EPOMIK
R-,? θko, EPOMIK R-, 301I, EP
OMIK 5R-33, EPOMIK R-3011E
% EPOMIK R-30gP.
EPOMIK R−307(以上三井石油化学エポΦシ
社製商品名); エピコート100八 エピコート10
0/FR、エピコー) 100コ、 エピコート100
’l。EPOMIK R-307 (product name manufactured by Mitsui Petrochemical Eposhi Co., Ltd.); Epicort 1008 Epicort 10
0/FR, Epicor) 100, Epicor 100
'l.
エピコート1004tK、エビコー) DX−3jX、
エピコート10θ7(以上シェル化学社製商品名);D
、E、R,l、 A /、 D、E、R,A4コ、 D
、E、R,t43U。Epicort 1004tK, Epicort) DX-3jX,
Epicote 10θ7 (trade name manufactured by Shell Chemical Co., Ltd.); D
, E, R, l, A /, D, E, R, A4, D
,E,R,t43U.
D、E、R,A/l、 D、E、R,AAダU、 D・
E、R,乙67(以上ダウ・ケミカル社製商品名)等が
代表的なものとして挙げられる。D, E, R, A/l, D, E, R, AA da U, D.
Typical examples include E, R, and Otsu67 (all trade names manufactured by Dow Chemical Company).
また粉体塗料組成物の一成分であるポリ酸4り無水物は
、エポキシ樹脂の硬化剤として使用されるもので一般式
(但し、Inはg〜/gの整数であり、nは2〜コ0の
整数である)
で示される融点3086以上の化合物でるる。Polyacid tetraanhydride, which is a component of the powder coating composition, is used as a curing agent for epoxy resin and has the general formula (where In is an integer of g~/g, and n is 2~ It is a compound with a melting point of 3086 or higher, which is an integer of 0.
なお、一般式中、m値がg未満になると、塗膜の伸び、
すなわち可撓性のある塗膜が得られず、曲げ加工性が悪
くなり、逆に/ざを越えると塗膜の硬さが低下するので
いずれも好ましくない。またn値が、−未満になると低
温硬化たおける塗膜性能が十分発(ボされず、逆に20
を越えると反応性が高まり、粉体塗料製造の溶融練合工
程で一部反応が進行し、塗膜1生能、貯蔵安定性に悪影
響を及ぼすので、いずれも好ましくない。In addition, in the general formula, when the m value is less than g, the elongation of the coating film,
That is, a flexible coating film cannot be obtained and bending workability deteriorates, and conversely, if the bending angle is exceeded, the hardness of the coating film decreases, which is not preferable. Also, if the n value is less than -, the coating film performance will be sufficiently developed when cured at low temperature (it will not be blotted, and on the contrary,
Exceeding this is not preferable because the reactivity increases and some reactions proceed during the melt-kneading step of powder coating production, which adversely affects the viability of the coating film and the storage stability.
またポリ酸ポリ無水物は、式で示すような直鎖の一+−
CH2−)−7−を有するものが望ましい。その他、一
部側鎖を有しているポリ酸ポリ無水物も使用し得る。In addition, polyacid polyanhydride is a linear 1+-
Those having CH2-)-7- are desirable. In addition, polyacid polyanhydrides partially having side chains can also be used.
またポリ酸ポリ無水物の融点は5060以上であること
が必須である。融点が5oOc未満になると常温で粉末
状を維持出来ないため好ましくない。Further, it is essential that the melting point of the polyacid polyanhydride is 5060 or higher. If the melting point is less than 5oOc, it is not preferable because the powder cannot be maintained at room temperature.
具体的には市販の08K−DA−8L−=OAH1O8
K−DA7SL−/2AHS、 08K−DA−8L−
,20AH−グ(以上間材製油社製商品名)等が代表的
なものとして挙げられる。Specifically, commercially available 08K-DA-8L-=OAH1O8
K-DA7SL-/2AHS, 08K-DA-8L-
, 20AH-G (trade name manufactured by Interzai Seishi Co., Ltd.) and the like are representative examples.
壕だ粉体塗料組成物の一成分であるトリフェニルホスフ
ィンは、低温・速硬化型粉体塗料として一応の目安とさ
れる、igoOc、so仕分間焼付条件でも優れた塗膜
性能を発揮させるために使用される。Triphenylphosphine, which is one of the components of the powder coating composition, is used to exhibit excellent coating film performance even under igoOc and SO sorting baking conditions, which is considered a rough guideline for low-temperature, fast-curing powder coatings. used for.
本発明で使用する粉体塗料は、前記のエポキシ樹脂、ポ
リ酸ポリ無水物及びトリフェニルホスフィンを必須構成
成分とするものである。The powder coating used in the present invention contains the above-mentioned epoxy resin, polyacid polyanhydride, and triphenylphosphine as essential components.
エポキシ樹脂と硬化剤としてのポリ酸ポリ無水物との配
合割合は、(,5−θ〜9.5−):(JO〜S)〔重
量基準〕が適当である。この範囲内で本来の樹脂特性が
発揮されるからでるる。The appropriate blending ratio of the epoxy resin and the polyacid polyanhydride as a curing agent is (,5-θ~9.5-):(JO~S) [by weight]. This is because the original resin properties are exhibited within this range.
またトリフェニルホスフィンの使用量は、エポキシ樹脂
とポリ酸ポリ無水物の合計量100重量部に対し/〜ダ
重瀘部が適当である。トリフェニルホスフィンの使用量
が7重量部未満になると低温硬化における塗膜性能が十
分発揮されず、逆にlIN量部を越えると耐腐食性等が
低下するので、いずれも好ましくない。The appropriate amount of triphenylphosphine to be used is about 100 parts by weight of the total amount of epoxy resin and polyanhydride. If the amount of triphenylphosphine used is less than 7 parts by weight, the coating film performance during low-temperature curing will not be sufficiently exhibited, and if it exceeds 1 part by weight, corrosion resistance etc. will deteriorate, so both are not preferred.
本発明で使用する粉体塗料組成物には、必要により、通
常粉体塗料に使用されている表面調整剤、タレ防止剤、
帯電防止剤等の添加剤; 二酸化チタン、 1波化鉄
、 カーボンブラック、 亜鉛粉末、 アルミニウム粉
末等の着色顔料; 硫酸バリウム、 炭酸カルシウム、
タルク、 シリカ、 ガラス繊維等の体質顔料; ノ
ボラック樹脂、 フェノキシ樹脂、 ブチラール樹脂、
ケトン樹脂、 ポリエステル樹脂等の改質樹脂;エポ
キシ化油、ジオクチルフタレート等の可塑剤等を有効量
で適宜加えることが出来る。The powder coating composition used in the present invention may contain, if necessary, surface conditioners, anti-sagging agents, etc., which are usually used in powder coatings.
Additives such as antistatic agents; Coloring pigments such as titanium dioxide, single wave iron, carbon black, zinc powder, and aluminum powder; Barium sulfate, calcium carbonate,
Extender pigments such as talc, silica, glass fiber; novolac resin, phenoxy resin, butyral resin,
Modified resins such as ketone resins and polyester resins; epoxidized oils, plasticizers such as dioctyl phthalate, etc. can be appropriately added in effective amounts.
本発明で使用する粉体塗料組成物を製造するだめの代表
的な方法としては、上記三成分及び必要によシ前罷の添
加剤、顔料、樹脂等を添加したものを粗混合した後、加
熱ニーダ−1加熱ロール、エクストルーダー等によシ通
常70〜/ダo0c程度で溶融混疎し、冷却後粉砕する
方法が使用し得る。このようにして得られる粉体塗料の
平均粒径は3θ〜/SOμが適当である。A typical method for producing the powder coating composition used in the present invention is to roughly mix the above three components and optional additives, pigments, resins, etc. A method may be used in which the mixture is melted and mixed using a heating roll, an extruder, etc. at a temperature of about 70 to 0.0 C, and then pulverized after cooling. The average particle size of the powder coating material obtained in this manner is suitably 3θ to /SOμ.
以上説明したエピクロルヒドリン−ビスフェノール型工
Iキシ樹脂、 ポリ酸ポリ無水物及びトリフェニルホス
フィンを必須成分として含有する、本発明で使用する粉
体塗料組成物は、曲げ刀V工件の優れた塗膜を形成する
ことが出来、また、溶融後のダル化時間が短かく、従っ
てリフロー性が少ないため異形鉄筋棒に適用した場合、
その凸部の形状が損なわれず、形状保持性が良く、さら
に高温においても貯蔵安定性に優れ、かつ低温、速硬化
可能であるという特徴を有しているので鉄筋棒用粉体塗
料として好適でるる。The powder coating composition used in the present invention, which contains the above-described epichlorohydrin-bisphenol type resin, polyacid polyanhydride, and triphenylphosphine as essential components, has a coating film with excellent bending properties. It also has a short dulling time after melting, and therefore has low reflow properties, so when applied to deformed reinforcing bars,
It is suitable as a powder coating for reinforcing bars because the shape of the convex part is not lost, it has good shape retention, it has excellent storage stability even at high temperatures, and it can be cured quickly at low temperatures. Ruru.
次に鉄筋棒の粉体塗装方法につき説明する。Next, the powder coating method for reinforcing bars will be explained.
鉄筋棒は、予めショツトブラスト、グリッドプラスト等
の表面処理をした後、加熱炉中で、予熱する。なお、本
発明において予熱せず、粉体塗料塗装後加熱する、いわ
ゆる後加熱方式でも可能ではあるが、塗膜中にディトが
生じやすく、それが、鉄筋棒の腐食原因をなるので、適
当ではない。The reinforcing bars are subjected to surface treatments such as shot blasting and grid blasting, and then preheated in a heating furnace. In addition, in the present invention, it is possible to use the so-called post-heating method in which heating is performed after powder coating is applied without preheating, but it is not suitable because it tends to cause detritus in the coating film and causes corrosion of the reinforcing bar. do not have.
予熱温度は、本発明で使用する粉体塗料組成物が/7θ
OC程度の低温で、充分反応硬化するため、/りOOC
程度でもよいが、鉄筋棒の温度低下を考慮して1108
0以上、好ましくは、200〜コSθ0Cが適当である
。The preheating temperature is such that the powder coating composition used in the present invention is /7θ
Because it fully reacts and hardens at a low temperature of about OC, / or OOC
It may be a certain degree, but considering the temperature drop of the reinforcing bar, 1108
Sθ0C of 0 or more, preferably 200 to 0C is appropriate.
次いで、粉体塗料組成物を通常粉体塗装に使用される静
電粉体スプレー塗装機等にて膜厚約gO〜2Sθμにな
るよう上記鉄筋棒に塗装する。なお、塗装後の後加熱は
特に必要ないが、適当な温度に後加熱しても何等差し支
えない。Next, the powder coating composition is applied to the reinforcing rod using an electrostatic powder spray coating machine or the like commonly used for powder coating to a film thickness of approximately gO to 2Sθμ. Note that post-heating after coating is not particularly necessary, but there is no problem with post-heating to an appropriate temperature.
第1因は、本発明の代表的な塗装状1m図を示すもので
ある。以下、この図を参照して、上記塗装方法を更に詳
しく1況明する。The first factor shows a 1 m diagram of a typical painted state of the present invention. Hereinafter, the above coating method will be explained in more detail with reference to this figure.
加I〜炉(図示せず)により予熱された異形鉄筋棒1は
コンペ“γ−を構成する回転ロール2によりrHil
;itさせ、遮蔽板3に囲゛まれた静電粉体スプレー塗
装機4により <−&装される。な2、オーバ−スフ0
レー粉体ゆ科は、コンベアーの下に設置した回収装置5
により回収される。The deformed reinforcing bar 1 preheated by a heating furnace (not shown) is heated by rotating rolls 2 constituting a competition "γ-".
; it is installed by an electrostatic powder spray coating machine 4 surrounded by a shielding plate 3. Na 2, overflow 0
The collection device 5 installed under the conveyor is used for collecting powder.
recovered by.
第1図に示す4装手段により異形鉄筋棒1は回転;」−
ル2,2′間の空間部で塗装されるため塗シ残し個所が
なくな多本発明の塗装方法として量適である。また静電
粉体スプレー塗装機4よ如手前に位置(図面では左側)
回転ロール2は異形鉄筋棒1の予熱温度が低下しないよ
う、内部に加熱手段を設置しておくとさらに好ましい。The deformed reinforcing bar 1 is rotated by the four mounting means shown in FIG.
Since the coating is applied in the space between the tiles 2 and 2', there is no uncoated area, making it suitable for the coating method of the present invention. Also, the electrostatic powder spray coating machine 4 is located in front (left side in the drawing).
It is further preferable that heating means be installed inside the rotating roll 2 so that the preheating temperature of the deformed reinforcing bar 1 does not decrease.
なお、静電粉体スプレー塗装機4によシ塗装された異形
鉄筋棒1が最初に接する回転ロール2′に到達するまで
に、塗膜硬化率約ダθ係以上硬化してないと回転ロール
2′に塗膜が付着したり、塗膜損傷が生じたシすること
がめる。そこで異形鉄筋棒の移動速度、すなわち回転ロ
ール2の回転速度あるいは回転ロール間隔距離を調節す
る必要がめる。すなわち塗装された異形鉄筋棒1が回転
ロール2′に到達するまでの時間は予熱温度、粉体塗料
組成物の配合割合等によシ変わるが、通常的30秒程度
が適当である。Note that by the time the deformed reinforcing bar 1 coated by the electrostatic powder spray coating machine 4 reaches the rotating roll 2' with which it comes into contact for the first time, the coating film must have been cured by a factor of about DA θ or more. 2' may have a paint film attached or damage to the paint film may occur. Therefore, it is necessary to adjust the moving speed of the deformed reinforcing bar, that is, the rotational speed of the rotating rolls 2 or the distance between the rotating rolls. That is, the time it takes for the coated deformed reinforcing bar 1 to reach the rotating roll 2' varies depending on the preheating temperature, the blending ratio of the powder coating composition, etc., but is usually about 30 seconds.
以上の通り、本発明の塗装方法は、粉体塗料組成物が貯
蔵安定性に優れ、かつ低温:速硬化可能であるので、塗
装作業性が非常に良く、しかも耐腐食性のみならず、曲
げ加工性、形状保持性等の優れた塗1漠を形成出来ると
いう特徴を有している。As described above, in the coating method of the present invention, the powder coating composition has excellent storage stability and can be cured quickly at low temperatures, so it has very good coating workability, and is not only corrosion resistant but also bendable. It has the characteristic of being able to form a coating with excellent workability and shape retention.
従って本発明の鉄筋棒の粉体塗装方法は、当業界に於て
至大な実用価値をもつものである。Therefore, the powder coating method for reinforcing bars of the present invention has great practical value in this industry.
以下、実施例によp本発明を更に詳細に説明する。なお
、実施例中1部」および「%」は重鎖基準である。Hereinafter, the present invention will be explained in more detail with reference to Examples. In the examples, "1 part" and "%" are based on heavy chain.
使用する粉体塗料組成物は、第7表に示す配合物をヘン
シェルミキサーで粗混合し、次いで二軸押出機にて溶融
練合し、これを冷却ロールで冷却した後、粉砕機にて微
粉砕し、/コOメツシュパスの粉体塗料を得ることによ
如調製した。The powder coating composition used is obtained by roughly mixing the formulations shown in Table 7 in a Henschel mixer, then melt-kneading in a twin-screw extruder, cooling it with a cooling roll, and then finely mixing it in a pulverizer. It was prepared by grinding to obtain a powder coating of /O mesh pass.
注/)粉体塗料A、C,D、E、F、G、H,Iエピコ
ートφ/θO+(シェル化学社製商品名)〔エポキシ当
縫9左O,融点10θ0C〕粉体塗料B
エピコート+ 10θ7(シェル化学社製商品名)〔エ
ポキシ当M:/qso、融点/コア°C]粉体塗料J
エピコートΦ1009(シェル化学社製商品名)〔エポ
キシ当j4.コ9SO9融点/!;O0C〕注2)粉体
塗料A、B、C,F、G、JO8K−DA−8L−20
AH(間材製油社製商品名)〔前記一般式のm=/’l
が約/θチ2m=/ざが約?Oチの混合物で、n−3−
,2<平均値)である酸無水物当量23g、融点9りQ
Cの化合物〕
粉体塗料D
O8K−DA−8L−/コAH(間材製油社製商品名)
〔前記一般式のm−10,ルー3.2 (平均値)で、
M無水物当−4/7/、融点glI0C〕粉体塗料E
O8K−DA−8L−コθAH−1I(間材製油社製商
品名)〔前記一般式のm=/’lが約10%、 rrL
=/lが約qθ%の混合物で、n=//(平均値)であ
る酸無水物当量300.融点/θ0°Cの化合物〕
粉体塗料H
ジシアンジアミド
粉体塗料I
テトラヒドロ無水7タル酸
注3)ノ?ラック樹脂(D、E、N、1g(ダウケミカ
ル社製商品名)〕
注4”)モタ70−(モンサンドケミカル社製i■品名
)実施例/
ショツトブラストで表面処理した直径/9mの異形鉄筋
棒を、静電粉体スプレー塗料グの下部に移動されてきた
時の温度が約2’100Cになるように加熱炉にて予熱
し、粉体塗料Aを乾燥膜厚約lSOμになるよう塗装し
た。なお、異形鉄筋棒1の移動速度は、粉体塗料Aを塗
装後、最初に接する回転ロール2′に接触するまでの時
間が30秒間になるように調節し、連続的に異形鉄筋棒
1を移動させながら塗装した。得られた塗膜の性能試験
結果を第2表、上欄に示した。Note/) Powder coating A, C, D, E, F, G, H, I Epicoat φ/θO+ (Product name manufactured by Shell Chemical Co., Ltd.) [Epoxy backstitch 9 left O, melting point 10θ0C] Powder coating B Epicoat + 10θ7 (trade name manufactured by Shell Chemical Co., Ltd.) [Epoxy weight M:/qso, melting point/core °C] Powder coating J Epicoat Φ1009 (trade name manufactured by Shell Chemical Co., Ltd.) [Epoxy weight J4. Ko9SO9 melting point/! ;O0C] Note 2) Powder coating A, B, C, F, G, JO8K-DA-8L-20
AH (product name manufactured by Mazai Oil Co., Ltd.) [m=/'l in the above general formula
is about /θchi2m=/zaga is about? A mixture of O, n-3-
, 2<average value), acid anhydride equivalent weight 23g, melting point 9riQ
Compound C] Powder coating D O8K-DA-8L-/CoAH (trade name manufactured by Mazashi Oil Co., Ltd.)
[In the general formula m-10, roux 3.2 (average value),
M anhydride equivalent -4/7/, melting point glI0C] Powder coating E O8K-DA-8L-ko θAH-1I (trade name manufactured by Interzai Oil Co., Ltd.) [m=/'l in the above general formula is approximately 10% , rrL
A mixture with =/l of about qθ% and an acid anhydride equivalent weight of n=//(average value) of 300. Compounds with melting point/θ0°C] Powder coating H Dicyandiamide powder coating I Tetrahydro-7-talic anhydride Note 3) No? Lac resin (D, E, N, 1 g (product name manufactured by Dow Chemical Company) Note 4") Mota 70- (product name manufactured by Monsando Chemical Company) Example / Surface treated with shot blasting Diameter / 9 m irregular shape Preheat the reinforcing bar in a heating furnace so that the temperature when it is moved to the bottom of the electrostatic powder spray coating is approximately 2'100C, and apply powder coating A to a dry film thickness of approximately 1SOμ. The moving speed of the deformed reinforcing bar 1 was adjusted so that the time from when the powder coating A was applied until it first contacted the rotating roll 2' was 30 seconds, and the deformed reinforcing bar 1 was continuously applied. The coating was carried out while moving the rod 1. The performance test results of the obtained coating film are shown in the upper column of Table 2.
また粉体塗料Aをポリエチレン製袋に入れ封をし、グ0
°Cの恒温器にls日間貯蔵した後、同様にして塗装し
、得られた塗膜の性能試験結果を第2表、下欄に示した
〇
実施例−〜り及び比較例/〜3
粉体塗料B、C,D、E、F、G、H,I、Jを使用し
て実施例/と同様にして塗装し、得られた塗膜の性能試
験結果を第2表に示した。Also, put powder paint A in a polyethylene bag and seal it.
After being stored in a constant temperature chamber at °C for 1s days, it was painted in the same manner, and the performance test results of the obtained coating film are shown in the lower column of Table 2. The body paints B, C, D, E, F, G, H, I, and J were coated in the same manner as in Examples, and the performance test results of the resulting paint films are shown in Table 2.
第 コ 表
注5)目視判定
○:良好 X:不良
注6)異形鉄筋棒の先端部を曲げ〔曲げ条件200C,
1,、D(曲げ直径)×1g0o(角度)〕、塗膜状態
を目視判定O:塗膜に異常なし、X:塗膜にクラック等
の異常有性7)曲げ加工性試験後の異形鉄筋棒につ@、
、>00時1司塩水噴霧試験した。Table C Note 5) Visual judgment ○: Good
1, D (bending diameter) x 1g0o (angle)] Visual judgment of coating film condition O: No abnormality in coating film, X: Abnormality such as cracks in coating film 7) Deformed reinforcing bar after bending workability test Stick @,
,>00:1: Salt water spray test was conducted.
○:異常なし、 ×:曲げ個所に錆が発生第2表よシ明
らかの如く、本発明の方法で得られた塗膜は、優れた塗
膜性能を有し、かつ粉体塗料の貯蔵安定性も優れていた
。○: No abnormality, ×: Rust occurred at bent portions As is clear from Table 2, the coating film obtained by the method of the present invention has excellent coating performance and is stable in storage as a powder coating. Her sex was also excellent.
一方、)!Jフェニルホスフィン融の少ない粉体塗料を
使用した比較例/、トリフェニルホスフィン量の過剰な
粉体塗料を使用した比較例コ、従来一般に利用されてい
るジシアンジアミド、テトラヒドロ無水フタル酸を硬化
剤とした粉体塗料を使用した比較例3.ダは、いずれも
曲げ加工性、耐腐食性とも不良であった。また融点の高
いエポキシ樹脂の粉体塗料を使用した比較例Sは塗面の
平滑性、曲げ加工性、耐腐食性とも不良でめった。on the other hand,)! JComparative example using a powder coating with low phenylphosphine melting/Comparative example using a powder coating with an excessive amount of triphenylphosphine, using the conventionally commonly used dicyandiamide and tetrahydrophthalic anhydride as curing agents Comparative example 3 using powder paint. Both the bending workability and corrosion resistance were poor. Furthermore, Comparative Example S, which used a powder coating made of an epoxy resin with a high melting point, failed in terms of the smoothness of the coated surface, poor bending workability, and poor corrosion resistance.
図は本発明の代表的塗装状態を示す正面図である。
図中、1は異形鉄筋棒、 2及び2′は回転ロール、
3は遮蔽板、 4は静電粉体スプレー塗装機、 5は回
収装置を示す。The figure is a front view showing a typical coating state of the present invention. In the figure, 1 is a deformed reinforcing bar, 2 and 2' are rotating rolls,
3 is a shielding plate, 4 is an electrostatic powder spray coating machine, and 5 is a collection device.
Claims (1)
シ基を有し、かつ融点がSO〜/1IOoCのエピクロ
ルヒドリン−ビスフェノール型エポキシ樹脂・・・・・
・・・・・・・30〜95重量%と(11) 一般式 (但し、mはg〜/gの整数であり、nはλ〜−〇の整
数である) で示される、融点3000以上のポリ酸ポリ無水物・・
・・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・ 5〜50重量%とからなる混合物・・・
・・・・・・・・・・・・ 100重量部と(B)トリ
フェニルホスフィン・・・/〜4’ iJI 量tll
sからなる粉体塗料組成物を塗装することを特徴とする
鉄筋棒の粉体塗装方法。[Claims] (A) (+) / Epichlorohydrin-bisphenol type epoxy resin having at least one epoxy group in the molecule and having a melting point of SO to /1IOoC on a reinforcing bar preheated to /'gOcC or more・・・・・・
...30 to 95% by weight and a melting point of 3000 or more, represented by the general formula (11) (where m is an integer of g to /g and n is an integer of λ to -〇) Polyacid polyanhydride...
・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・ A mixture consisting of 5 to 50% by weight...
・・・・・・・・・・・・ 100 parts by weight and (B) triphenylphosphine.../~4' iJI amount tll
1. A method for powder coating a reinforcing bar, the method comprising coating a reinforcing bar with a powder coating composition consisting of s.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12146883A JPS6014971A (en) | 1983-07-04 | 1983-07-04 | Powder coating method of reinforcing bar |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12146883A JPS6014971A (en) | 1983-07-04 | 1983-07-04 | Powder coating method of reinforcing bar |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6014971A true JPS6014971A (en) | 1985-01-25 |
| JPH0315504B2 JPH0315504B2 (en) | 1991-03-01 |
Family
ID=14811892
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12146883A Granted JPS6014971A (en) | 1983-07-04 | 1983-07-04 | Powder coating method of reinforcing bar |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6014971A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS621468A (en) * | 1985-06-28 | 1987-01-07 | High Frequency Heattreat Co Ltd | Method and apparatus for painting deformed bar |
| JP2015188784A (en) * | 2014-03-27 | 2015-11-02 | 第一高周波工業株式会社 | Film manufacturing method and film manufacturing apparatus for reinforcing bar with fixing unit |
-
1983
- 1983-07-04 JP JP12146883A patent/JPS6014971A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS621468A (en) * | 1985-06-28 | 1987-01-07 | High Frequency Heattreat Co Ltd | Method and apparatus for painting deformed bar |
| JP2015188784A (en) * | 2014-03-27 | 2015-11-02 | 第一高周波工業株式会社 | Film manufacturing method and film manufacturing apparatus for reinforcing bar with fixing unit |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0315504B2 (en) | 1991-03-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2206481C (en) | Cathodic disbondment resistant epoxy powder coating composition and reinforcing steel bar coated therewith | |
| JPH0628940B2 (en) | Chip resistant coating | |
| US3007888A (en) | Epoxy resin base protective surfaces | |
| JP3511051B2 (en) | Low temperature curing type powder coating composition and method for forming coating film on inner surface of metal tube using this powder coating composition | |
| JPS6014971A (en) | Powder coating method of reinforcing bar | |
| JPS5825391B2 (en) | Flexible epoxy resin powder composition | |
| JPH0412842A (en) | Durable coated metal plate | |
| JPS6019943B2 (en) | Anticorrosive coating composition | |
| JPS60250075A (en) | Powder coating composition for reinforcing iron rod | |
| EP0551063B1 (en) | Use of protective coating compositions for underbody coatings | |
| EP1900782A1 (en) | Acid resistant high temperature coating | |
| JP2000109728A (en) | Powder coating composition capable of being cured at wide baking temperature range and its coating application | |
| JPH0619060B2 (en) | Anti-chipping coating composition | |
| JPS63172777A (en) | Chipping-resistant coating composition | |
| JPH0526833B2 (en) | ||
| JPS63451B2 (en) | ||
| JP3183079B2 (en) | Paint composition and painted metal sheet with excellent wear resistance | |
| JPS6044350B2 (en) | Anticorrosive coating composition | |
| JPS6211779A (en) | Corrosive agent of emulsion baking type | |
| JPS6176567A (en) | paint composition | |
| JPH0681711B2 (en) | Anticorrosion coating method | |
| JPH09100425A (en) | Powder paint for casting | |
| JPS6097075A (en) | Preparation of double layer coated steel pipe | |
| JPS5945365A (en) | Epoxy resin powder paint | |
| JPS6166766A (en) | anti-corrosion paint |