JPH0574625B2 - - Google Patents
Info
- Publication number
- JPH0574625B2 JPH0574625B2 JP2748685A JP2748685A JPH0574625B2 JP H0574625 B2 JPH0574625 B2 JP H0574625B2 JP 2748685 A JP2748685 A JP 2748685A JP 2748685 A JP2748685 A JP 2748685A JP H0574625 B2 JPH0574625 B2 JP H0574625B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- aluminum
- fin
- composition
- polyvinyl alcohol
- 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.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 12
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 10
- OERNJTNJEZOPIA-UHFFFAOYSA-N zirconium nitrate Chemical compound [Zr+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O OERNJTNJEZOPIA-UHFFFAOYSA-N 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 229920000877 Melamine resin Polymers 0.000 claims description 8
- 239000004640 Melamine resin Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 229910052782 aluminium Inorganic materials 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 239000010408 film Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000008119 colloidal silica Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- -1 amine salt Chemical class 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 241001163841 Albugo ipomoeae-panduratae Species 0.000 description 1
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- 239000005696 Diammonium phosphate Substances 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- LNEUSAPFBRDCPM-UHFFFAOYSA-N carbamimidoylazanium;sulfamate Chemical compound NC(N)=N.NS(O)(=O)=O LNEUSAPFBRDCPM-UHFFFAOYSA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- WOAZEKPXTXCPFZ-UHFFFAOYSA-N dimethyl(phenyl)azanium;chloride Chemical compound Cl.CN(C)C1=CC=CC=C1 WOAZEKPXTXCPFZ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Description
〔産業上の利用分野〕
本発明は、熱交換器のフイン材の表面にコーテ
イングするための組成物に関するものである。
〔従来の技術〕と〔発明が解決しようとする問題
点〕
従来、熱交換器、特にフイン付熱交換器におい
ては、フイン材としてアルミニウムが広く用いら
れている。この様なフイン付熱交換器にあつて
は、その効率改善のためにフインの伝熱面積を増
大させる必要があるが、その際に、スペースの制
約からフインピツチの縮小化も同時におこなつた
場合には、通風抵抗の増大、特にフインにおける
凝縮水による風圧損失が増大し、通風量の低下、
騒音の発生、凝縮水の前面飛散といつた問題が生
じる。従つてフイン付熱交換器の効率改善、省ス
ペースにはフインにおける凝縮水による風圧損失
の低下方法が重要な決め手となる。
フインにおける凝縮水による風圧損失は、熱交
換器をエバポレータとして用いる場合、フイン表
面温度が空気の露点以下となり、空気中の水分が
凝縮し、この凝縮水のフイン表面への付着、ひい
てはフイン間における凝縮水のブリツジ現象によ
り風路が狭められて発生するものである。
従つて前記圧損失を少なくするには、フイン表
面の凝縮水を常に取り除けば良いわけであるが、
その方法として次の二通りが考えられる。
即ち、フイン表面を完全に揆水化して凝縮した
水滴をころがり落とす方法と、フイン表面を親水
化(水ぬれ性付与)して水滴を薄い水膜として流
下させる方法である。現実的には、通常得られる
揆水化処理フインは、実機でテストすると凝縮水
の排除が不充分な場合が多い。一方親水化処理
は、凝縮した水分を拡張ぬれにより薄い水膜とし
てフイン表面に沿つて流下させるものであり、ク
ロメート処理、ベーマイト処理、水溶性高分子コ
ート法などの諸法が実際に提案されている。この
ような親水化処理フインに於ては、親水化のため
に基材のアルミニウムまたはアルミニウム合金が
水分により腐食する危険性が大きいから耐腐食性
化が特に強く要求されるものである。アルミニウ
ム材料が水分により腐食を受けると水酸化アルミ
ニウムの一種である白色粉末(いわゆる白錆)が
発生し、乾燥状態では室内に逸散して衛生上も問
題になるからである。
従つて熱交換器用アルミニウムフイン材料に於
ては、その表面の親水性を高めて凝縮水を薄膜と
し、凝縮水による風圧損失を極力少なくすると共
に、強固な耐食性を有するものとすることが肝要
である。
従来、フイン材用として、親水性および耐食性
を有する皮膜層を設けたアルミニウム材が種々提
案されているが、これらは、皮膜形成に高温で長
時間を要する;腐食性については、例えば塩水噴
霧試験で200〜300時間の範中にあり、300時間以
上のものは出現していない;また、加工性に関し
ても、例えば100万個以上の製品加工に耐えきれ
ず、製品にクラツクを発生する。或いは処理に際
し煩雑な工程、例えば皮膜形成後に更に中和や水
洗工程を経なければならないなど;未だ問題点が
多い。
本発明者らは、かゝる問題点に鑑み、水ぬれ性
がよく、耐食性、加工性、耐溶剤性の優れた熱交
換器用アルミニウム材料を経済的に提供せんがた
め先に珪素化合物と周期表第2−b族、第3−b
族又は第6−b族の元素の化合物であつて、珪素
化合物とともにアルカリ下に水に溶解可能な無機
化合物と、熱硬化性の水溶性高分子化合物とから
なることを特徴とするフイン材コーテイング用組
成物に係る特許を出願中であるが、更に鋭意研究
を進めた結果上記特性の中でも特に加工性がより
優ぐれたフイン材コーテイング用組成物の発明に
到達した。
〔問題点を解決するための手段〕と〔作用〕
即ち、本発明はポリビニルアルコール、硝酸ジ
ルコン、水溶性メラミン樹脂及びその硬化触媒か
ら成る水溶液並びに該水溶液中に分散せしめた水
溶性無機粉体から成ることを特徴とするフイン材
コーテイング用組成物である。
本発明のポリビニルアルコールとしては、市販
の完全鹸化型、中間鹸化型、部分鹸化型のいずれ
も使用可能であるが、フイン材としての性能を再
現よく製造する目的では完全鹸化型を用いること
が好ましい。
本発明の水溶性メラミン樹脂は市販の単量体樹
脂、及び縮重合度が或る程度進んだダイマー型樹
脂のいずれを使用しても良い。
メラミン樹脂の硬化触媒としては塩化アンモ
ン、第二燐酸アンモン、スルフアミン酸アンモン
等のアンモニウム塩系触媒、有機アミノアルコー
ルの塩酸又はスルフアミン酸塩、その他ジメチル
アニリン塩酸塩、ピリジン−塩酸系、ピリコン−
モンクロル酢酸などの有機アミン塩系触媒、塩化
マグネシウム、塩化亜鉛、硫酸亜鉛等の無機金属
系触媒を挙げることが出来る。中でも有機アミン
塩系触媒の使用が好ましい。
本発明における水不溶性の無機粉体としては、
水に不溶か又は溶解度が極めて小さく且つ親水性
保有の粉体であれば良く、例えば水酸化亜鉛、水
酸化アルミニウム、水酸化カルシウム、水酸化
鉄、水酸化銅、水酸化マグネシウム、コロイダル
シリカ等を挙げることが出来る。これら無機粉体
の中でも、とりわけコロイダルシリカが適切であ
る。
本発明の組成物の調製にあたつては、例えばポ
リビニルアルコールと硝酸ジルコニウムを水に溶
解してA液とする。A液とは別に水溶性メラミン
樹脂とその硬化触媒とを水に溶解してB液とす
る。次にA液とB液とを混合し、その中に水不溶
性の無機粉体、必要に応じて更に金属キレート化
剤、顔料、染料、増粘剤等を添加して強力攪拌を
おこない脱泡すればよい。
本発明の組成物に於ける各成分の量的割合は、
特に定めるものではないが硝酸ジルコンの量はポ
リビニルアルコール100重量部に対して2〜10重
量部、好ましくは4〜7重量部である。本成分の
量が少な過ぎると、ポリビニルアルコールの不溶
化が不完全であり、多過ぎると、皮膜の親水性が
不足して凝縮水の排除が不充分となる。
水溶性メラミン樹脂の量は、ポリビニルアルコ
ール100重量部に対して50〜200重量部、好ましく
は80〜180重量部である。本成分の量が少な過ぎ
ると、フイン材との接着力が減少する傾向があ
り、多過ぎると、皮膜の親水性が不足して上記と
同様凝縮水の排除が不充分となる。無機粉体はポ
リビニルアルコール100重量部に対して50〜200重
量部、好ましくは70〜150重量部である。本成分
の量が少な過ぎると、皮膜が湿潤、乾燥を繰り返
すうち、親水性を失い易く、多過ぎると、透明性
を失い商品として価値観を損ずる。
本成分の粒子径は通常篩いで、320メツシユを
通過するものを用いることが前提となるが、それ
以上に微粉末を使用することが好結果を得る。
フイン材との接着力を増強させる目的で5−ス
ルホサリチン酸、エチレンジアミンテトラ醋酸ト
ランス−シクロヘキサン−1,2ジアミンテトラ
醋酸等の金属キレート化剤を本発明の組成物に添
加しても良い。
本発明の組成物を用いて、アルミニウム又はア
ルミニウム合金薄板からなるフイン材の表面に親
水性皮膜を形成するには、前述のようにして調製
した本発明の組成物の水溶性をフイン材の表面に
コーテイングするとか、前記水溶液中にフイン材
を浸漬するとかしてフイン材の表面に本発明の組
成物のと塗膜を形成し、必要に応じ、ローラーに
よるしごき処理やエアーブロー等によつて過剰の
水溶液を除去し、最後に熱処理して塗膜の硬化を
はかればよい。この熱処理は、例えば200℃〜250
℃にセツトした熱風乾燥機中で30〜60秒間乾燥し
てなすことができる。
フイン材は、その表面が油性物質にて汚染され
ていない限り特に、本発明の組成物の塗布に先だ
つて前処理を行なう必要はない。
〔実施例〕
次に本発明を実施例等に基づいて更に具体的に
説明する。
実験例 1〜14
脱脂を完了した厚さ0.15m/mのJIS A−1100
アルミニウム薄板を、寸法200m/m×300m/m
に切断した。一方、メラミン樹脂(日本カーバイ
ト工業株式会社製;商品ニカレジン)5gを水30
gに溶解し更に触媒としてスルフアミン酸グワニ
ジン1gを加えた溶液にあらかじめ用意されたポ
リビニルアルコール(信越化学工業株式会社製品
種C−17)5%及び硝酸ジルコン0.05%〜0.5%
を含む水溶液を適宜混合して、メラミン樹脂をポ
リビニルアルコール100重量部に対して50〜200重
量部の範囲になるように加え、更にコロイダルシ
リカ(日本エアロジル工業株式会社製品種
COK84)をポリビニルアルコール100重量部に対
して20〜200重量部の範囲になるように加えて第
1−1表の成分組成から成る総成分濃度10%の水
溶液を調製した。次いでこの水溶液に、前述のア
ルミニウム薄板を浸漬し、その後取出し、過剰の
水溶液を除去してから250℃の熱風乾燥機中で30
秒間乾燥して処理製品を得た。
以上の如くして得た処理製品について、ぬれ性
を示す指標として接触角の測定、耐食性を示す指
標として塩水噴霧試験、耐溶剤性を示す指標とし
てトリクレン浸漬試験、作業性を示す指標として
オイル試験と加工試験を夫々行ない、更に耐冷熱
性についても試験を行ない品質特性を測定した。
これら試験等の結果については第1−2表に示
す。
[Industrial Application Field] The present invention relates to a composition for coating the surface of a fin material of a heat exchanger. [Prior Art] and [Problems to be Solved by the Invention] Conventionally, aluminum has been widely used as a fin material in heat exchangers, particularly heat exchangers with fins. In such a heat exchanger with fins, it is necessary to increase the heat transfer area of the fins in order to improve the efficiency, but at the same time, due to space constraints, it is necessary to reduce the fin pitch at the same time. This is due to an increase in ventilation resistance, especially an increase in wind pressure loss due to condensed water on the fins, and a decrease in ventilation volume.
Problems such as noise generation and front splashing of condensed water occur. Therefore, in order to improve the efficiency and save space of heat exchangers with fins, the method of reducing wind pressure loss due to condensed water in the fins is an important deciding factor. Wind pressure loss due to condensed water on the fins is caused by the fact that when the heat exchanger is used as an evaporator, the surface temperature of the fins becomes below the dew point of the air, moisture in the air condenses, and this condensed water adheres to the surface of the fins, resulting in damage between the fins. This occurs when the air passage is narrowed due to the bridging phenomenon of condensed water. Therefore, in order to reduce the pressure loss, it is sufficient to constantly remove the condensed water on the fin surface.
There are two possible ways to do this: Specifically, there are two methods: one is to make the fin surface completely water-repellent so that the condensed water droplets roll off, and the other is to make the fin surface hydrophilic (impart water wettability) so that the water droplets flow down as a thin water film. In reality, normally obtained water repellent fins are often found to be insufficient in removing condensed water when tested in actual equipment. On the other hand, hydrophilic treatment involves causing condensed water to flow down the fin surface as a thin water film through expansion wetting, and various methods such as chromate treatment, boehmite treatment, and water-soluble polymer coating methods have actually been proposed. There is. In such hydrophilized fins, there is a strong risk that the aluminum or aluminum alloy of the base material will be corroded by moisture due to the hydrophilic treatment, so corrosion resistance is particularly strongly required. This is because when aluminum materials are corroded by moisture, white powder (so-called white rust), which is a type of aluminum hydroxide, is generated, and in dry conditions, it escapes into the room and poses a sanitary problem. Therefore, it is important for the aluminum fin material for heat exchangers to have high hydrophilicity on its surface to form a thin film for condensed water, to minimize wind pressure loss due to condensed water, and to have strong corrosion resistance. be. Conventionally, various aluminum materials with hydrophilic and corrosion-resistant film layers have been proposed for use as fin materials, but these require long periods of time at high temperatures to form the film; for example, salt spray tests have been conducted to test corrosion resistance. In terms of processability, for example, it cannot withstand processing of more than 1 million products, resulting in cracks in the product. Alternatively, there are still many problems such as complicated processing steps such as neutralization and water washing steps after film formation. In view of these problems, the inventors of the present invention aimed to economically provide an aluminum material for heat exchangers that has good water wettability, excellent corrosion resistance, workability, and solvent resistance. Table 2-b group, 3-b
A fin material coating comprising an inorganic compound which is a compound of an element of Group 6 or Group 6-b and is soluble in water under an alkali together with a silicon compound, and a thermosetting water-soluble polymer compound. As a result of further intensive research, we have arrived at the invention of a composition for coating fin materials, which has particularly excellent processability among the above properties. [Means for solving the problem] and [effect] That is, the present invention provides an aqueous solution comprising polyvinyl alcohol, zirconium nitrate, a water-soluble melamine resin, and a curing catalyst thereof, and a water-soluble inorganic powder dispersed in the aqueous solution. A composition for coating a fin material, characterized in that: As the polyvinyl alcohol of the present invention, any commercially available completely saponified type, intermediate saponified type, or partially saponified type can be used, but it is preferable to use the completely saponified type for the purpose of manufacturing with good reproducibility of performance as a fin material. . The water-soluble melamine resin of the present invention may be either a commercially available monomer resin or a dimer type resin with a certain degree of condensation polymerization. Curing catalysts for melamine resin include ammonium salt catalysts such as ammonium chloride, diammonium phosphate, and ammonium sulfamate, hydrochloric acid or sulfamate salts of organic amino alcohols, dimethylaniline hydrochloride, pyridine-hydrochloric acid, and pyricone.
Examples include organic amine salt catalysts such as monochloroacetic acid, and inorganic metal catalysts such as magnesium chloride, zinc chloride, and zinc sulfate. Among them, it is preferable to use an organic amine salt catalyst. The water-insoluble inorganic powder in the present invention includes:
Any powder that is insoluble or has extremely low solubility in water and has hydrophilic properties may be used, such as zinc hydroxide, aluminum hydroxide, calcium hydroxide, iron hydroxide, copper hydroxide, magnesium hydroxide, colloidal silica, etc. I can list them. Among these inorganic powders, colloidal silica is particularly suitable. In preparing the composition of the present invention, for example, polyvinyl alcohol and zirconium nitrate are dissolved in water to prepare a solution A. Separately from liquid A, a water-soluble melamine resin and its curing catalyst are dissolved in water to obtain liquid B. Next, liquid A and liquid B are mixed, water-insoluble inorganic powder, metal chelating agents, pigments, dyes, thickeners, etc. are added as needed, and vigorous stirring is performed to defoam. do it. The quantitative proportions of each component in the composition of the present invention are:
Although not particularly specified, the amount of zirconium nitrate is 2 to 10 parts by weight, preferably 4 to 7 parts by weight, based on 100 parts by weight of polyvinyl alcohol. If the amount of this component is too small, the insolubilization of polyvinyl alcohol will be incomplete, and if it is too large, the hydrophilicity of the film will be insufficient and the removal of condensed water will be insufficient. The amount of water-soluble melamine resin is 50 to 200 parts by weight, preferably 80 to 180 parts by weight, based on 100 parts by weight of polyvinyl alcohol. If the amount of this component is too small, the adhesive force with the fin material tends to decrease, and if it is too large, the hydrophilicity of the coating will be insufficient, resulting in insufficient removal of condensed water as described above. The amount of the inorganic powder is 50 to 200 parts by weight, preferably 70 to 150 parts by weight, based on 100 parts by weight of polyvinyl alcohol. If the amount of this component is too small, the film tends to lose its hydrophilicity as it repeats wetting and drying, and if it is too large, it loses transparency and impairs its value as a product. The particle size of this component is normally one that passes through a 320 mesh sieve, but better results can be obtained by using a finer powder than that. A metal chelating agent such as 5-sulfosalicic acid, ethylenediaminetetraacetic acid, trans-cyclohexane-1,2diaminetetraacetic acid, etc. may be added to the composition of the present invention for the purpose of enhancing the adhesive strength with the fin material. In order to form a hydrophilic film on the surface of a fin material made of aluminum or an aluminum alloy thin plate using the composition of the present invention, the water solubility of the composition of the present invention prepared as described above is determined on the surface of the fin material. A coating film of the composition of the present invention is formed on the surface of the fin material by coating the fin material or by immersing the fin material in the aqueous solution, and if necessary, remove excess by ironing with a roller, air blowing, etc. The aqueous solution is removed, and the coating film is finally cured by heat treatment. This heat treatment is carried out at 200°C to 250°C, for example.
It can be dried for 30 to 60 seconds in a hot air dryer set at ℃. The fin material does not need to be pretreated prior to application of the composition of the present invention, unless the surface thereof is contaminated with oily substances. [Example] Next, the present invention will be described in more detail based on Examples. Experimental examples 1 to 14 JIS A-1100 with a thickness of 0.15m/m after degreasing
Aluminum thin plate, dimensions 200m/m x 300m/m
It was cut into On the other hand, add 5 g of melamine resin (manufactured by Nippon Carbide Kogyo Co., Ltd.; product Ni-Resin) to 30 ml of water.
5% of polyvinyl alcohol (Shin-Etsu Chemical Co., Ltd. product type C-17) and 0.05% to 0.5% of zirconium nitrate were dissolved in 5% of polyvinyl alcohol (Shin-Etsu Chemical Co., Ltd. product type C-17) and 1g of guanidine sulfamate was added as a catalyst.
melamine resin in a range of 50 to 200 parts by weight per 100 parts by weight of polyvinyl alcohol, and colloidal silica (Japan Aerosil Industries Co., Ltd. product type).
COK84) was added to 100 parts by weight of polyvinyl alcohol in an amount ranging from 20 to 200 parts by weight to prepare an aqueous solution with a total component concentration of 10% having the component composition shown in Table 1-1. Next, the aluminum thin plate mentioned above was immersed in this aqueous solution, then taken out, excess aqueous solution was removed, and then dried in a hot air dryer at 250°C for 30 minutes.
A treated product was obtained by drying for a second. Regarding the treated products obtained as described above, contact angle measurement was performed as an indicator of wettability, salt spray test was performed as an indicator of corrosion resistance, trichlene immersion test was performed as an indicator of solvent resistance, and oil test was performed as an indicator of workability. Processing tests were conducted on each, and cold and heat resistance tests were also conducted to measure quality characteristics.
The results of these tests are shown in Table 1-2.
【表】【table】
【表】【table】
【表】
実験例 13〜17
次の第2−1表に示す組成物を調製し、実験例
−1〜12と同様にアルミニウム板表面にコートし
てアルミニウムフイン材を作成し、その性能を測
定した結果2−2表に示す如くいずれも良好なフ
イン材特性を示した。[Table] Experimental Examples 13 to 17 The compositions shown in Table 2-1 below were prepared and coated on the surface of an aluminum plate in the same manner as Experimental Examples 1 to 12 to create an aluminum fin material, and its performance was measured. As shown in Table 2-2, all of the fin materials exhibited good properties.
【表】【table】
【表】
*1〜*6の意味は第1−2表に同じ
〔発明の効果〕
本発明は、以上の如く、水ぬれ性、耐食性、加
工性、耐溶剤性等の諸性質においてすぐれた、新
規なフイン材コーテイング用組成物を提供するも
のであり、産業利用性の高いものである。[Table] The meanings of *1 to *6 are the same as in Table 1-2 [Effects of the invention] As described above, the present invention has excellent properties such as water wettability, corrosion resistance, processability, and solvent resistance. , provides a novel composition for coating fin materials, which has high industrial applicability.
Claims (1)
性メラミン樹脂及びその硬化触媒から成る水溶液
並びに該水溶液中に水散せしめた水不溶性無機粉
体から成ることを特徴とするフイン材コーテイン
グ用組成物。1. A composition for coating fin materials, comprising an aqueous solution comprising polyvinyl alcohol, zirconium nitrate, a water-soluble melamine resin, and a curing catalyst thereof, and a water-insoluble inorganic powder dispersed in the aqueous solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2748685A JPS61185570A (en) | 1985-02-13 | 1985-02-13 | Composition for coating fin materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2748685A JPS61185570A (en) | 1985-02-13 | 1985-02-13 | Composition for coating fin materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61185570A JPS61185570A (en) | 1986-08-19 |
| JPH0574625B2 true JPH0574625B2 (en) | 1993-10-18 |
Family
ID=12222455
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2748685A Granted JPS61185570A (en) | 1985-02-13 | 1985-02-13 | Composition for coating fin materials |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61185570A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63262238A (en) * | 1987-04-20 | 1988-10-28 | スカイアルミニウム株式会社 | Heat-exchanger fin material |
| JP2709391B2 (en) * | 1988-03-02 | 1998-02-04 | 日本製箔株式会社 | Compositions and paints with excellent far-infrared radiation properties |
| US5012862A (en) * | 1990-09-12 | 1991-05-07 | Jw Aluminum Company | Hydrophilic fins for a heat exchanger |
| JP2649297B2 (en) * | 1991-09-18 | 1997-09-03 | 三菱アルミニウム株式会社 | Paint composition, painted fin material, and method for producing fin material |
| US5137067A (en) * | 1991-12-16 | 1992-08-11 | Jw Aluminum Company | Hydrophilic and corrosion resistant fins for a heat exchanger |
-
1985
- 1985-02-13 JP JP2748685A patent/JPS61185570A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61185570A (en) | 1986-08-19 |
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