JPH01299877A - Surface treating agent for heat exchanger aluminum fin and its treatment - Google Patents
Surface treating agent for heat exchanger aluminum fin and its treatmentInfo
- Publication number
- JPH01299877A JPH01299877A JP12909588A JP12909588A JPH01299877A JP H01299877 A JPH01299877 A JP H01299877A JP 12909588 A JP12909588 A JP 12909588A JP 12909588 A JP12909588 A JP 12909588A JP H01299877 A JPH01299877 A JP H01299877A
- Authority
- JP
- Japan
- Prior art keywords
- water
- surface treatment
- urea resin
- polyamide resin
- treatment agent
- 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.)
- Pending
Links
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 22
- 229910052782 aluminium Inorganic materials 0.000 title claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 40
- 229920001807 Urea-formaldehyde Polymers 0.000 claims abstract description 20
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 18
- 239000007787 solid Substances 0.000 claims abstract description 13
- 239000012756 surface treatment agent Substances 0.000 claims description 18
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 15
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 238000004381 surface treatment Methods 0.000 claims description 6
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims description 5
- 238000003618 dip coating Methods 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 5
- 238000007654 immersion Methods 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- 229920002292 Nylon 6 Polymers 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- -1 methylol groups Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 description 10
- 235000019645 odor Nutrition 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- 241001163841 Albugo ipomoeae-panduratae Species 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- UWIVMLUBHUNIBC-MJSUFJGSSA-N dcaa Chemical compound Cl.CN1C2=CC=CC=C2C2([C@@H](C34)OC(=O)CCl)[C@@H]1[C@@H]1CC3[C@H](CC)[C@@H](OC(=O)CCl)N1[C@H]4C2 UWIVMLUBHUNIBC-MJSUFJGSSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloro-acetic acid Natural products OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 1
- KHEMNHQQEMAABL-UHFFFAOYSA-J dihydroxy(dioxo)chromium Chemical compound O[Cr](O)(=O)=O.O[Cr](O)(=O)=O KHEMNHQQEMAABL-UHFFFAOYSA-J 0.000 description 1
- WMYWOWFOOVUPFY-UHFFFAOYSA-L dihydroxy(dioxo)chromium;phosphoric acid Chemical compound OP(O)(O)=O.O[Cr](O)(=O)=O WMYWOWFOOVUPFY-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 238000013101 initial test Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- DSKJXGYAJJHDOE-UHFFFAOYSA-N methylideneurea Chemical compound NC(=O)N=C DSKJXGYAJJHDOE-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はアルミニウム熱交換器フィン材の表面処理に関
するものでさらに詳しくは、アルミニウム表面を親水化
し」水滴の発生を抑制もしくは防止するに有効である表
面処理剤および処理方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to surface treatment of aluminum heat exchanger fin materials, and more specifically, the present invention relates to surface treatment of aluminum heat exchanger fin materials. This invention relates to a certain surface treatment agent and treatment method.
[従来の技術]
空調機の熱交換器は冷房時に発生する凝縮水の結露によ
って起る不具合、例えば通風抵抗の増大による電力の損
失、騒音の発生、水滴の飛散などを防止する対策として
、アルミニウムフィン材の表面親水化処理が施されてい
る。かかる処理を行う方法として、アルミニウム材を成
型加工してフィンを作成し、このものを組立てた後に、
表面処理剤を浸漬塗布する方法がある。この方法で実用
化されているものとして例えば、無機皮膜を形成させる
方法として、クロメート膜〜アルカリケイ酸塩処理(特
開昭59−13078号公報)、有機皮膜を形成させる
方法としてクロメート膜〜ポリアミド樹脂膜形成(特開
昭61−250495号公報)等が挙げられる。前者の
ケイ酸塩系の処理では、親木性は良好で水との接触角も
20°以下を保つが、特有の臭気があり、さらに、皮膜
の分解による微粉末の飛散があり、また細菌、カビが発
育し易く、これらによる異臭を発生しやすいといった問
題がある。一方、後者のポリアミド樹脂膜の形成による
方法では、臭気の問題は少いが、耐水性が十分でなく、
またコスト高であるという問題がある。[Prior Art] Heat exchangers for air conditioners are made of aluminum as a measure to prevent problems caused by condensation of condensed water during cooling, such as loss of power due to increased ventilation resistance, generation of noise, and scattering of water droplets. The surface of the fin material has been treated to make it hydrophilic. As a method for performing such processing, fins are created by molding aluminum material, and after this is assembled,
There is a method of dip coating a surface treatment agent. This method has been put into practical use, for example, as a method for forming an inorganic film, chromate film - alkali silicate treatment (Japanese Patent Application Laid-open No. 13078/1982), and as a method for forming an organic film, chromate film - polyamide treatment. Examples include resin film formation (Japanese Unexamined Patent Publication No. 61-250495). The former silicate-based treatment has good wood-philicity and maintains a contact angle with water of 20 degrees or less, but it has a unique odor, and furthermore, it causes the scattering of fine powder due to the decomposition of the film, and it is also susceptible to bacteria. There are problems in that molds are likely to grow, and molds are likely to generate unpleasant odors. On the other hand, the latter method, which involves forming a polyamide resin film, has fewer odor problems, but does not have sufficient water resistance.
Another problem is that the cost is high.
[発明が解決しようとする課題]
空調機は近年小型軽量化が進んでおり、熱交換器もコン
パクト設計の為フィン間隔が小さくなり、より高い親水
性を要求され、水との接触角30°以下であることが必
須となってきている。[Problem to be solved by the invention] Air conditioners have become smaller and lighter in recent years, and heat exchangers have also become compact in design, so the spacing between fins has become smaller, and higher hydrophilicity is required, with a contact angle of 30° with water. The following has become essential.
また快適居住空間の提供を目的とする為、最近は臭気の
発生が問題視されている。前述のように現在実用化され
ている浸漬型処理剤ではかかる要請に十分応えられるも
のでない、従って、本発明は、臭気の点で有利な有機樹
脂系であって、かつより親水性に優れた表面処理剤およ
び浸漬による表面処理方法を開発することを目的とする
。Furthermore, since the purpose is to provide a comfortable living space, the generation of odor has recently become a problem. As mentioned above, the immersion-type treatment agents currently in practical use cannot sufficiently meet such demands. Therefore, the present invention aims to develop an organic resin system that is advantageous in terms of odor and has better hydrophilicity. The purpose is to develop surface treatment agents and surface treatment methods by dipping.
[課題を解決するための手段]
本発明によれば、ポリビニルアルコール、水溶性ポリア
ミドおよび尿素樹脂を含有する表面処理剤により、熱交
換器を浸漬、焼付処理することにより、親水性の優れた
皮膜をアルミニウム表面に形成できる。[Means for Solving the Problems] According to the present invention, a film with excellent hydrophilic properties can be formed by dipping and baking a heat exchanger with a surface treatment agent containing polyvinyl alcohol, water-soluble polyamide, and urea resin. can be formed on aluminum surfaces.
すなわち、本発明は、完全ケン化タイプのポリビニルア
ルコール、水溶性ポリアミド樹脂、尿素樹脂および水を
含有する熱交換器アルミフィン用の表面処理剤、および
上記表面処理剤を固形分濃度2〜10重量%とした浴に
てアルミフィンを浸漬塗装することを特徴とする熱交換
器アルミフィンの表面処理方法を提供するものである。That is, the present invention provides a surface treatment agent for heat exchanger aluminum fins containing completely saponified polyvinyl alcohol, water-soluble polyamide resin, urea resin, and water, and the above surface treatment agent at a solid content of 2 to 10% by weight. The present invention provides a method for surface treatment of aluminum fins of a heat exchanger, which is characterized in that the aluminum fins are dip-coated in a bath with a concentration of 50%.
本発明における表面処理剤の成分の一つであるポリビニ
ルアルコール(以下、rPVAJと略記する。)は造膜
成分として主要な役割を果たすとともに分子中に二級水
酸基が多量に存在するため水との親和性に富み、さらに
この水酸基と他の構成4分との相互作用により耐水性と
親木持続性を維持する作用を示す、かかる目的に適合す
るのは一般にケン化度98%以上である完全ケン化タイ
プのPVAである。この材料は常温下における水に対す
る溶解度が低く、室温度以下で使用される熱交換器アル
ミニウム材に形成する皮膜として好ましい性質を示す、
またPVAの重合度は500以上のものが、後述のポリ
アミド樹脂との分子的絡み合いによる親水性の持続、及
び耐水性の点から好ましい。Polyvinyl alcohol (hereinafter abbreviated as rPVAJ), which is one of the components of the surface treatment agent in the present invention, plays a major role as a film-forming component and has a large amount of secondary hydroxyl groups in its molecules, so it is difficult to interact with water. Compatible with this purpose is generally one with a degree of saponification of 98% or more, which has a high affinity and also maintains water resistance and parent tree sustainability through the interaction of this hydroxyl group with other constituent components. It is saponified type PVA. This material has low solubility in water at room temperature, and exhibits desirable properties as a film formed on aluminum heat exchangers used below room temperature.
Further, it is preferable that the degree of polymerization of PVA is 500 or more, from the viewpoint of maintaining hydrophilicity due to molecular entanglement with the polyamide resin described below and water resistance.
本発明処理剤の他の構成4分である水溶性ポリアミド樹
脂は本発明における親水性の付与に重要な役割を果たす
、前記のPVAは、単独では加熱により部分結晶化が起
こり疎水性を示すものであるが、適切な第2成分の添加
により、加熱による結晶化が抑制され、親水性を維持す
ることができる。そのような役割を果す成分として本発
明者は水溶性ポリアミド樹脂が最適であることを見出し
た。さらにPVAとポリアミド樹脂の混合比率が1:0
.5〜2の範囲で、高い親水性を付与し、かつ耐水性も
維持できることを見出した。この目的に使用される水溶
性ポリアミド樹脂は、ナイロン−6を水及び/又はアル
コールに可溶性にしたものであって、市販の樹脂、例え
ばAQナイロンA−90、A−70、P−70、など(
東し■製)を好適に使用することができる。水溶性ポリ
アミド樹脂単独では親水性の優れた皮膜を形成するもの
の水に再溶解する。なおポリアミド樹脂の安定溶解のた
め、適量の中和剤(リン酸等)、もしくはアルコール系
溶剤を加えることが好ましい。The water-soluble polyamide resin, which is another component of the treatment agent of the present invention, plays an important role in imparting hydrophilicity in the present invention.The above-mentioned PVA, when used alone, undergoes partial crystallization when heated and exhibits hydrophobicity. However, by adding an appropriate second component, crystallization due to heating can be suppressed and hydrophilicity can be maintained. The present inventors have found that water-soluble polyamide resin is optimal as a component that plays such a role. Furthermore, the mixing ratio of PVA and polyamide resin is 1:0.
.. It has been found that in the range of 5 to 2, high hydrophilicity can be imparted and water resistance can also be maintained. The water-soluble polyamide resin used for this purpose is nylon-6 soluble in water and/or alcohol, and commercially available resins such as AQ nylon A-90, A-70, P-70, etc. (
(manufactured by Toshi ■) can be suitably used. Although a water-soluble polyamide resin alone forms a film with excellent hydrophilic properties, it is redissolved in water. In order to stably dissolve the polyamide resin, it is preferable to add an appropriate amount of a neutralizing agent (such as phosphoric acid) or an alcoholic solvent.
上記PVAとポリアミド樹脂のみでもかなり耐水性の良
い親水性皮膜を形成できるが、さらに耐水性、親木持続
性を向上させるため1本発明においては架橋剤として尿
素樹脂を使用する一通常架橋剤としてよく使用される水
溶性メラミン樹脂、フェノール樹脂、エポキシ樹脂等は
骨格中の非極性成分の影響で、親水性を著しく損う、こ
れに対し尿素樹脂は骨格が極性に富み親水性を阻害する
程度が小さい。尿素樹脂は一般に尿素とホルマリンとの
付加縮合物であるが、付加縮合反応が充分に行なわれず
低分子量のメチロール尿素が多く存在する場合、および
反応時のホルマリンの量が少なく不溶性メチレン尿素が
多く存在する場合には水溶性ないしは水分散性が劣り沈
澱を生じるため好ましくない。本発明における尿素樹脂
は水溶性ないしは水分散性である必要があり、特に、尿
素とホルマリンとの付加縮合反応時に低級アルコール(
例えばメタノール、エタノール等)を添加し、メチロー
ル基の一部ないしは全部をアルキルエーテル化したもの
は水溶性に優れ希釈安定性も良好であり好ましい、一般
に10重量%以下の、固形分濃度の低いところで使用す
る浸漬処理においては、希釈安定性の点などから尿素樹
脂として上記アルキルエーテル化尿素樹脂を使用するこ
とが特に好ましい。Although it is possible to form a hydrophilic film with fairly good water resistance using just the PVA and polyamide resin mentioned above, in order to further improve the water resistance and the persistence of parent wood, in the present invention, a urea resin is used as a crosslinking agent. Commonly used water-soluble melamine resins, phenolic resins, epoxy resins, etc. significantly impair hydrophilicity due to the influence of non-polar components in their skeletons, whereas urea resins have highly polar skeletons that impede hydrophilicity. is small. Urea resin is generally an addition condensation product of urea and formalin, but when the addition condensation reaction is not carried out sufficiently and a large amount of low molecular weight methylol urea is present, or when the amount of formalin during the reaction is small and there is a large amount of insoluble methylene urea. If this is the case, the water solubility or water dispersibility will be poor and precipitation will occur, which is not preferable. The urea resin used in the present invention needs to be water-soluble or water-dispersible, and in particular, lower alcohol (
For example, those in which some or all of the methylol groups are converted into alkyl ethers by adding methanol, ethanol, etc. have excellent water solubility and good dilution stability, and are preferred at low solid content concentrations, generally 10% by weight or less. In the dipping treatment used, it is particularly preferable to use the alkyl etherified urea resin as the urea resin from the viewpoint of dilution stability.
尿素樹脂の配合比は固形分重量比で、
PVA:尿素樹脂が1 :0.Of〜0.5.さらには
l:0.1〜0.3の範囲であることが好ましい。The blending ratio of urea resin is solid content weight ratio: PVA:urea resin: 1:0. Of~0.5. Furthermore, it is preferable that 1 is in the range of 0.1 to 0.3.
水は前記のPVA、水溶性ポリアミド樹脂および尿素樹
脂を溶解ないしは分散、希釈するため用いられる。Water is used to dissolve, disperse, and dilute the PVA, water-soluble polyamide resin, and urea resin.
本発明に従った熱交換器アルミフィン用の表面処・理剤
は前記した必須成分に加えて、顔料、界面活性剤、消泡
剤、アルコール系溶剤、pH調整剤(酸、アルカ1月な
どの汎用の任意成分を含むことができる。In addition to the above-mentioned essential ingredients, the surface treatment agent for heat exchanger aluminum fins according to the present invention includes pigments, surfactants, antifoaming agents, alcoholic solvents, pH adjusters (acids, alkalis, etc.). It can contain any general purpose ingredients.
本発明に従った表面処理剤は特に浸漬塗装に対して優れ
た適性を示すものであるが、処理剤の濃度を適当に調整
することによりロールコート、スプレーコートにも適用
可能である。Although the surface treatment agent according to the present invention shows particularly excellent suitability for dip coating, it can also be applied to roll coating and spray coating by appropriately adjusting the concentration of the treatment agent.
浸漬塗装する場合には、処理剤の固形分濃度を通常2〜
lO重量%の範囲に調整した浴とし、この浴にてアルミ
フィンを浸漬塗装する。浸漬塗装するアルミフィンは通
常、予め成型、組立てられた熱交換器アルミフィンであ
り、このものを洛中に浸漬し、引上げた後、適当な焼付
条件、例えば150〜200℃で10〜30分間焼付け
ることによって塗布量0.2〜5μ層、好ましくは0.
5〜3μIの親水性皮膜を得ることができる。When applying dip coating, the solid content concentration of the treatment agent is usually 2 to 2.
A bath is adjusted to a range of 10% by weight, and aluminum fins are dip coated in this bath. The aluminum fins to be dip coated are usually pre-formed and assembled heat exchanger aluminum fins, which are immersed in water, pulled up, and baked under appropriate baking conditions, for example, at 150 to 200°C for 10 to 30 minutes. By applying a coating amount of 0.2 to 5μ layer, preferably 0.2μ layer.
A hydrophilic film of 5 to 3 μI can be obtained.
本発明に従った表面処理剤は脱脂、洗浄されたアルミフ
ィン無処理材へ塗布することによっても実用的な親水性
皮膜を形成するが、アルミフィン材としてリン酸クロメ
ート処理又はクロム酸クロメート処理等の化成処理を施
した化成処理アルミフィン材を使用し、このものに本発
明表面処理剤を塗布し親水性皮膜を形成することが耐食
□性等の点から好ましい。The surface treatment agent according to the present invention forms a practical hydrophilic film by applying it to untreated aluminum fin materials that have been degreased and cleaned. It is preferable from the viewpoint of corrosion resistance etc. to use a chemical conversion treated aluminum fin material which has been subjected to chemical conversion treatment, and to apply the surface treatment agent of the present invention to this material to form a hydrophilic film.
実施例
以下、実施例および比較例にて本発明を具体的に説明す
る。以下、1%」は「重量%」を意味する。EXAMPLES The present invention will be specifically explained below using examples and comparative examples. Hereinafter, "1%" means "wt%".
実施例1〜7および比較例1〜4
試験用のアルミニウム基材として厚さ0. 1龍、幅7
0+u+、長さ150關のAA3003薄扱を用い、こ
のものを40℃の温水で湯洗、さらに40℃の2%苛性
ソーダ水溶液に2分間浸漬し脱脂・洗浄を行なった後、
水洗を行なった。Examples 1 to 7 and Comparative Examples 1 to 4 An aluminum base material with a thickness of 0. 1 dragon, width 7
Using a thin piece of AA3003 with a length of 0+u+ and a length of 150 mm, it was washed with hot water at 40°C, and then immersed in a 2% caustic soda aqueous solution at 40°C for 2 minutes to degrease and wash.
I washed it with water.
このものを、第1表に示したように、■化成処理せずに
無処理のままで使用、■リン酸クロメート処理(日本パ
ーカー社製[アルクロム3701J)をCr付着量が約
100mg/rr?となるように施して使用、または■
クロム酸クロ方法を用いた。As shown in Table 1, this material was used as is without any chemical conversion treatment, and was treated with phosphoric acid chromate (Alchromate 3701J, manufactured by Nippon Parker Co., Ltd.) so that the amount of Cr deposited was approximately 100 mg/rr? Use it so that it becomes, or ■
The chromic acid chromate method was used.
ついで、上記無処理扱又は化成処理板を第1表に示した
配合の表面処理剤洛中に浸漬塗装し、ついで熱風乾燥炉
で150℃で30分間焼付けを行ない、皮膜重量的1
g/rn’の親水性皮膜を形成した。Next, the above-mentioned untreated or chemically treated board was dip-coated in a surface treatment agent having the composition shown in Table 1, and then baked in a hot air drying oven at 150°C for 30 minutes to achieve a coating weight of 1.
A hydrophilic film of g/rn' was formed.
得られた表面処理板の試験結果を第1表に示す。Table 1 shows the test results of the surface treated plate obtained.
なお、第1表に示した配合中の(註)は以下のとおりで
ある。Notes in the formulation shown in Table 1 are as follows.
*1. z気化学工業■製、完全ケン化(〉98%)
ポバール(100%固形分)
*2. 電気化学工業■製、部分ケン化(88〜9%)
ポバール(100%固形分)
本3.4東し■製、水溶性ポリアミド樹脂(100%固
形分)
*5. 大日本インキ化学工業■製、水溶性メチルエー
テル化尿素樹脂(70%固形分)*6. 三井東圧化学
■製、水溶性メチルエーテル化尿素樹脂(65%固形分
)
第1表における試験方法および評価方法は下記のとおり
である。*1. Manufactured by ZKikagaku Kogyo ■, fully saponified (>98%)
Poval (100% solids) *2. Manufactured by Denki Kagaku Kogyo ■, partially saponified (88-9%)
Poval (100% solids) Made by Hon 3.4 Toshi ■, water-soluble polyamide resin (100% solids) *5. Manufactured by Dainippon Ink & Chemicals ■, water-soluble methyl etherified urea resin (70% solids) *6. Water-soluble methyl etherified urea resin (65% solids) manufactured by Mitsui Toatsu Chemical ■ The test methods and evaluation methods in Table 1 are as follows.
[試験および評価方法]
水濡性:水濡性は試験板を水道水に30秒間浸漬、引上
げた時の水濡面積率で評価した。[Test and evaluation method] Water wettability: Water wettability was evaluated by the water wet area ratio when a test plate was immersed in tap water for 30 seconds and pulled out.
0:水濡面積率 100%
O: l/ 90〜100%未満Δ: 〃
50〜90%未満
X: // 50%未満接触角:試
験板に約0.03ccの脱イオン水の水滴を形成し、2
0℃にて水滴の接触角を協和科学■製コンタククンゲル
メーターDCAA型にて測定した。なお水濡性および接
触角は、初期試験板および水道水流水中に500時間浸
漬し、引上げ後、20℃、75%R,Hの環境下に24
時間放置した流水浸漬試験板についても行なった。0: Water wet area ratio 100% O: l/ less than 90-100% Δ: 〃
50 to less than 90%
The contact angle of the water droplet was measured at 0° C. using a contact angle meter DCAA model manufactured by Kyowa Kagaku ■. The water wettability and contact angle were determined by immersing the initial test plate in running tap water for 500 hours, pulling it up, and then placing it in an environment of 20°C, 75% R, H for 24 hours.
The tests were also carried out on test plates immersed in running water that had been left for an extended period of time.
耐水溶解性=24時間、約15℃の水道水に浸漬前後の
重量差から計算した。Water solubility = Calculated from the weight difference before and after immersion in tap water at about 15° C. for 24 hours.
水溶解重(%)=((初期皮膜重量−
24時間浸漬後の皮膜重量)
/初期皮膜重量)X100
O:水溶解重 5%未満
○: 〃 5〜lO%未満
△: 〃 10〜20%未満
X:// 20%以上
耐食性:JIS Z 2371塩水噴霧試験300
時間後の平面部における白錆発生の面積率で評価した。Water dissolved weight (%) = ((Initial film weight - Film weight after 24 hours immersion) /Initial film weight) Less than X: // 20% or more Corrosion resistance: JIS Z 2371 salt spray test 300
Evaluation was made based on the area ratio of white rust on the flat surface after a period of time.
0:白錆発生面積率 0〜1 %未満Q :
/l l −w l 0%未満処理液の安定
性:表面処理剤をガラス容器に取りふたをして室温にl
O日間放置後、凝集、沈降物の有無等の変化を評価した
。0: White rust occurrence area rate 0 to less than 1% Q:
/l l -w l Less than 0% Stability of treatment solution: Place the surface treatment agent in a glass container, cover with a lid, and let it cool to room temperature.
After standing for 0 days, changes such as aggregation and the presence or absence of sediment were evaluated.
0:変化なし
○:わずかに濁りが認められる
[発明の効果]
以上説明した通り、本発明に従った表面処理剤を熱交換
器アルミフィンに適用した場合、初期親水性及び流水浸
漬後の親木持続性がともに良好であり、かつ耐水溶解性
も良好な皮膜が得られる。0: No change ○: Slight turbidity observed [Effects of the invention] As explained above, when the surface treatment agent according to the present invention is applied to heat exchanger aluminum fins, initial hydrophilicity and hydrophilicity after immersion in running water A film can be obtained that has both good durability on wood and good water and solubility resistance.
また化成処理の併用により優れた耐食性の親水化処理板
が得られる。更に本発明に係る表面処理剤は珪酸塩を含
まないため悪臭等の不快感がなく、また、希釈安定性に
も優れているため、低濃度で使用する浸漬塗装の処理剤
としても優れた適応性を示すものである。Moreover, by combining the chemical conversion treatment, a hydrophilic treated plate with excellent corrosion resistance can be obtained. Furthermore, since the surface treatment agent according to the present invention does not contain silicate, there is no unpleasant odor or other unpleasant sensations, and it also has excellent dilution stability, making it excellently applicable as a treatment agent for dip coating used at low concentrations. It indicates gender.
Claims (1)
ポリアミド樹脂、尿素樹脂およ び水を含有する熱交換器アルミフィン用の 表面処理剤。 2)ポリビニルアルコール:ポリアミド樹脂:尿素樹脂
が固形分重量比で、1:0.5〜 2:0.01〜0.5である請求項1記載 の表面処理剤。 3)完全ケン化タイプのポリビニルアルコール、水溶性
ポリアミド樹脂、尿素樹脂およ び水を含有する固形分濃度2〜10重量% の表面処理剤浴にてアルミフィンを浸漬塗 装することを特徴とする熱交換器アルミ フィンの表面処理方法。 4)浸漬塗装するアルミフィンが予めリン酸クロメート
又はクロム酸クロメートで処理さ れたものである請求項3記載の表面処理方 法。[Claims] 1) A surface treatment agent for heat exchanger aluminum fins containing completely saponified polyvinyl alcohol, water-soluble polyamide resin, urea resin, and water. 2) The surface treatment agent according to claim 1, wherein the solid content weight ratio of polyvinyl alcohol: polyamide resin: urea resin is 1:0.5 to 2:0.01 to 0.5. 3) A heat exchange method characterized by dip-coating aluminum fins in a surface treatment agent bath containing completely saponified polyvinyl alcohol, water-soluble polyamide resin, urea resin, and water with a solid content concentration of 2 to 10% by weight. Surface treatment method for aluminum fins. 4) The surface treatment method according to claim 3, wherein the aluminum fin to be dip coated is previously treated with chromate phosphate or chromate chromate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12909588A JPH01299877A (en) | 1988-05-26 | 1988-05-26 | Surface treating agent for heat exchanger aluminum fin and its treatment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12909588A JPH01299877A (en) | 1988-05-26 | 1988-05-26 | Surface treating agent for heat exchanger aluminum fin and its treatment |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01299877A true JPH01299877A (en) | 1989-12-04 |
Family
ID=15000951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12909588A Pending JPH01299877A (en) | 1988-05-26 | 1988-05-26 | Surface treating agent for heat exchanger aluminum fin and its treatment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01299877A (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0326381A (en) * | 1989-06-23 | 1991-02-04 | Nippon Parkerizing Co Ltd | Heat exchanger made of aluminum and production thereof |
EP0413260A2 (en) * | 1989-08-11 | 1991-02-20 | Nippon Paint Co., Ltd. | Surface treatment chemicals for forming hydrophilic coatings, treatment bath containing them, and treatment method |
JPH0347570A (en) * | 1989-07-14 | 1991-02-28 | Nippon Parkerizing Co Ltd | Hydrophilic treatment of aluminum fin coil material |
US5350445A (en) * | 1991-06-12 | 1994-09-27 | Nippon Paint Co., Ltd. | Hydrophilic coating composition and bath containing same |
US5470431A (en) * | 1990-08-20 | 1995-11-28 | Showa Aluminum Corp. | Stack type evaporator |
US5494705A (en) * | 1993-01-06 | 1996-02-27 | Nippon Paint Co., Ltd. | Hydrophilic surface treating aqueous solution, hydrophilic surface treating method and hydrophilic surface treating film |
US5514248A (en) * | 1990-08-20 | 1996-05-07 | Showa Aluminum Corporation | Stack type evaporator |
EP0713240A2 (en) | 1994-11-17 | 1996-05-22 | Sumitomo Metal Mining Company Limited | Transparent conductor film for electric field shielding |
US5800673A (en) * | 1989-08-30 | 1998-09-01 | Showa Aluminum Corporation | Stack type evaporator |
JP2002292329A (en) * | 2001-04-02 | 2002-10-08 | Toyo Riken Kk | Method for lustering and stainproofing treatment of hard surface |
US6689481B2 (en) | 2000-11-10 | 2004-02-10 | Nihon Parkerizing Co., Ltd. | Aluminum alloy heat exchanger resistive to tobacco odor impregnation |
US6698507B2 (en) | 2002-01-11 | 2004-03-02 | Nihon Parkerizing Co., Ltd. | Aluminum alloy heat exchanger resistive to tobacco odor impregnation |
WO2009093541A1 (en) | 2008-01-24 | 2009-07-30 | Nippon Light Metal Company, Ltd. | Coated metal material |
WO2012165494A1 (en) * | 2011-05-31 | 2012-12-06 | 関西ペイント株式会社 | Hydrophilic coating material composition and hydrophilizing method |
JP2017071720A (en) * | 2015-10-08 | 2017-04-13 | 日本パーカライジング株式会社 | Surface treatment agent, coating film, and surface treatment method |
WO2018207416A1 (en) | 2017-05-08 | 2018-11-15 | 日本軽金属株式会社 | Aluminum coated material and method for producing same |
-
1988
- 1988-05-26 JP JP12909588A patent/JPH01299877A/en active Pending
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0326381A (en) * | 1989-06-23 | 1991-02-04 | Nippon Parkerizing Co Ltd | Heat exchanger made of aluminum and production thereof |
JPH0347570A (en) * | 1989-07-14 | 1991-02-28 | Nippon Parkerizing Co Ltd | Hydrophilic treatment of aluminum fin coil material |
EP0413260A2 (en) * | 1989-08-11 | 1991-02-20 | Nippon Paint Co., Ltd. | Surface treatment chemicals for forming hydrophilic coatings, treatment bath containing them, and treatment method |
US5800673A (en) * | 1989-08-30 | 1998-09-01 | Showa Aluminum Corporation | Stack type evaporator |
US5470431A (en) * | 1990-08-20 | 1995-11-28 | Showa Aluminum Corp. | Stack type evaporator |
US5514248A (en) * | 1990-08-20 | 1996-05-07 | Showa Aluminum Corporation | Stack type evaporator |
US5350445A (en) * | 1991-06-12 | 1994-09-27 | Nippon Paint Co., Ltd. | Hydrophilic coating composition and bath containing same |
US5494705A (en) * | 1993-01-06 | 1996-02-27 | Nippon Paint Co., Ltd. | Hydrophilic surface treating aqueous solution, hydrophilic surface treating method and hydrophilic surface treating film |
EP0713240A2 (en) | 1994-11-17 | 1996-05-22 | Sumitomo Metal Mining Company Limited | Transparent conductor film for electric field shielding |
US6689481B2 (en) | 2000-11-10 | 2004-02-10 | Nihon Parkerizing Co., Ltd. | Aluminum alloy heat exchanger resistive to tobacco odor impregnation |
JP2002292329A (en) * | 2001-04-02 | 2002-10-08 | Toyo Riken Kk | Method for lustering and stainproofing treatment of hard surface |
US6698507B2 (en) | 2002-01-11 | 2004-03-02 | Nihon Parkerizing Co., Ltd. | Aluminum alloy heat exchanger resistive to tobacco odor impregnation |
WO2009093541A1 (en) | 2008-01-24 | 2009-07-30 | Nippon Light Metal Company, Ltd. | Coated metal material |
WO2012165494A1 (en) * | 2011-05-31 | 2012-12-06 | 関西ペイント株式会社 | Hydrophilic coating material composition and hydrophilizing method |
JP2017071720A (en) * | 2015-10-08 | 2017-04-13 | 日本パーカライジング株式会社 | Surface treatment agent, coating film, and surface treatment method |
WO2018207416A1 (en) | 2017-05-08 | 2018-11-15 | 日本軽金属株式会社 | Aluminum coated material and method for producing same |
US12060643B2 (en) | 2017-05-08 | 2024-08-13 | Nippon Light Metal Company, Ltd. | Coated aluminum material and method for producing same |
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