JPS6158507B2 - - Google Patents
Info
- Publication number
- JPS6158507B2 JPS6158507B2 JP13642477A JP13642477A JPS6158507B2 JP S6158507 B2 JPS6158507 B2 JP S6158507B2 JP 13642477 A JP13642477 A JP 13642477A JP 13642477 A JP13642477 A JP 13642477A JP S6158507 B2 JPS6158507 B2 JP S6158507B2
- Authority
- JP
- Japan
- Prior art keywords
- wax
- weight
- parts
- powder
- composition
- 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
Links
- 239000001993 wax Substances 0.000 claims description 25
- 239000000843 powder Substances 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 7
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 3
- 239000004200 microcrystalline wax Substances 0.000 claims description 3
- 239000003223 protective agent Substances 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 210000003608 fece Anatomy 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000003608 radiolysis reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009287 sand filtration Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
本発明は物品の表面保護剤組成物に関するもの
である。
自動車や大型機械は屋外に保管したり、木箱や
ケースで包装することなく鉄道、船舶、トラツク
などで輸送するためにその外面の塗装面やメツキ
部分は接触によるすり傷や大気中からの降下物、
例えば鉄粉、煤煙、粉塵、鳥糞などによる汚染に
よつて美観が損われたり、塩分を含む風雨や酸性
物質などによつてメツキ部分の発錆腐食などの損
傷を受けることがあり、大きな問題となつてい
る。これらの損傷を防止するすぐれた保護方法が
要望されている。しかも、この保護方法には保護
が必要なくなつた時に容易に除去出来ることも強
く要望されている。
これらの要望に対して、従来より多くの方法が
検討されており、多くの特許がある。従来より検
討されている方法の長所欠点を表1に示す。表1
からもわかるように保護能力と除去の容易さは相
反する性質のため、未だ充分なものがないのが現
状である。
本発明者らは、従来の方法の長所欠点を十分に
検討した結果、本発明を完成した。本発明の組成
物は、ワツクス2〜98重量部、融点が100℃以上
で水に不溶性または難溶性で、かつ粒子径100μ
以下の有機物及び/または無機物の粉末1〜49重
量部、分子量100000以下の四弗化エチレン重合体
粉末(以下TFE重合体という)1〜49重量部を
含むことが特徴であり、ワツクスを塗布する方法
の良好な保護能力を維持し、かつ、除去の容易さ
を付与したものである。
The present invention relates to a surface protectant composition for articles. Automobiles and large machinery are stored outdoors or transported by train, ship, truck, etc. without being wrapped in wooden boxes or cases, so their painted or plating surfaces are susceptible to scratches due to contact or falling from the atmosphere. thing,
For example, contamination from iron powder, soot, dust, bird droppings, etc. can impair the aesthetic appearance, and wind and rain containing salt, acidic substances, etc. can cause damage such as rusting and corrosion of the plating parts, which is a major problem. It is becoming. There is a need for improved protection methods to prevent these damages. Moreover, it is strongly desired that this protection method be able to be easily removed when the protection is no longer needed. In response to these demands, many methods have been studied and many patents have been published. Table 1 shows the advantages and disadvantages of the methods that have been studied so far. Table 1
As can be seen from the above, protection ability and ease of removal are contradictory properties, so there is currently no sufficient product available. The present inventors have completed the present invention after thoroughly studying the advantages and disadvantages of conventional methods. The composition of the present invention contains 2 to 98 parts by weight of wax, has a melting point of 100°C or higher, is insoluble or sparingly soluble in water, and has a particle size of 100 μm.
It is characterized by containing 1 to 49 parts by weight of the following organic and/or inorganic powders and 1 to 49 parts by weight of tetrafluoroethylene polymer powder (hereinafter referred to as TFE polymer) with a molecular weight of 100,000 or less, and is coated with wax. This method maintains good protection ability and provides ease of removal.
【表】【table】
【表】
さらに詳細に説明すると、本発明のもつとも重
要な点はワツククス中にTFE重合体を含むこと
である。従来よりワツクスの塗布による方法の除
去性改良のためワツクス中に各種有機物や無機物
の粉末を含有させたものが考えられているが、多
量の粉末を含有させなければならないため、ワツ
クスの塗布による方法のすぐれた保護性が損なわ
れてしまい、特にサビや鳥糞等の浸透性のあるも
のに対する保護性は半減もしくはほとんどないも
のとなつてしまう。またワツクス中に少量の粉末
の添加では除去性の向上は認められない。本発明
者らはこの点を改良すべく種々検討した結果、本
発明の如くワツクス中にTFE重合体を含有させ
ることによりすぐれた保護能力と容易な除去性を
併せもつ組成物を作り得ることを見出した。
TFEの重合物としては、重合度により液体から
固体まで多くの種類があるが本発明には、一般に
TFEワツクスとよばれるように外観は粉末であ
るが、金属面や塗装面に均一に圧着させた場合ワ
ツクス的な性質を有するTFE重合体がもつとも
適当である。
本発明におけるTFE重合体の代わりに従来よ
り使用されている高分子量のTFEポリマーの粉
末を使用した場合には(比較例6)撥水性に効果
は認められるものの、保護剤として要求される重
要な性質は向上しない。これに対してTFE重合
体を用いた場合には(実施例1、2)耐薬品性、
非粘着性、撥水、撥油性等の付与効果が著しく、
かつ除去性にも優れているのである。
また、比較的低分子量のエチレン、プロピレン
重合体粉末を用いた場合にはこれらにワツクスと
の相溶性がある為ワツクス中に溶解してしまい除
去性の効果が期待できない。
このようにTFE重合体が一般の無機物、有機
ポリマー、オリゴマーに見られない特異な性質を
有することを見出し、これをワツクスに添加した
ことが本発明の特徴であり、さらに融点が100℃
以上で水に不溶性または難溶性で、かつ粒子径
100μ以下の有機物及び/または無機物の粉末を
併用添加することにより従来では得られなかつた
表面保護剤としてのすぐれた保護性を保持しかつ
必要のなくなつた場合、容易な除去性を有する本
発明品が得られたのである。
本発明の組成物における各成分の混合比率は保
護能力の要求度合、除去性の要求度合によつて決
定されるが一般的にワツクス2〜98重量部、融点
が100℃以上で水に不溶性または難溶性で、かつ
粒子径100μ以下の有機物及び/または無機物の
粉末1〜49重量部、TFE重合体1〜49重量部に
することが必要である。
ワツクスは少なくとも2重量部以上含有しない
と連続的な保護膜の形成が不十分で保護能力が低
下する。また、98重量部以上ではワツクスのみの
性能と同じになり除去が困難である。
融点が100℃以上で水に不溶性または難溶性
で、かつ粒子径100μ以下の有機物及び/または
無機物の粉末は少なくとも1重量部以上含有しな
いとTFE重合体のワツクス的な性質のみが現わ
れ除去性の向上が認められない。49重量部以上含
有する場合は剥離し易くなり保護能力が極度に低
下する。
TFE重合体は少なくとも1重量部以上含有し
ないと耐薬品性、非粘着性、撥水、撥油性が付与
されない。49重量部以上含有した場合は、TFE
重合体の粉末的性質が強くなり剥離し易くなり保
護能力が低下する。
本発明に使用出来るワツクスとしては各種鉱物
性ワツクス、動植物性ワツクス、硬化油脂、合成
ワツクス等の単独もしくは混合物であるが、除去
の容易さから融点40〜90℃程度のものが好まし
く、さらに好ましくは50〜70℃のセミマイクロク
リスタリンワツクスである。
有機物及び/または無機物粉末としては、
TFE重合体と共存し、これを共同して保護膜の
保護性を維持しつつ、膜に脆さを与えて剥離し易
くする作用を有する点で粉末状であることが必要
であり、さらに融点が100℃以上で水に不溶性ま
たは難溶性でかつ粒子径が100μ以下であること
が必要である。これらの条件は加熱等、組成物の
使用に際して必要であるとともに粒子径が上記よ
り大きいと保護能力が不十分となる。また、塗布
する際の分散媒に不溶であることが必要である。
例としては、有機物粉末として、ナイロン、ポリ
エチレン、フエノール樹脂等の高分子化合物の粉
末無機物粉末として炭酸カルシウム、タルク、無
水珪酸、ベントナイト、ウンモ等がある。価格供
給の容易さから炭酸カルシウム、タルク、ベント
ナイトが適当である。
TFE重合体としては、一般にTFEワツクスと
称されるもので概ね分子量約100000程度以下で、
粉末となるもの、即ち概ね分子量約1000程度以上
のもので、その製法としてはテロメル化によるも
の、熱分解によるもの、放射線分解によるもの等
のいずれでも良いが、分散性の点から粒子径50μ
以下、好ましくは20μ以下のものが良い。
本発明の組成物を保護すべき表面に塗布する方
法としては、揮発性の溶剤中に溶解けん濁して使
用することが作業性の点から好ましい。揮発性の
溶剤は、塗布する表面の状態(材質)により決め
るべきであり、これらの表面を侵すものであつて
はならない。一般的に脂肪族炭化水素系溶剤が望
ましい。溶剤の使用量は塗布条件により決めるべ
きであるが、少なすぎるとゲル化を起すために少
なくとも上記混合物100重量部に対して100重量部
使用する必要がある。また多量の溶剤の使用は経
済性、公害問題の点から不利である。よつて上記
混合物100重量部に対して100〜300重量部程度に
することが望ましい。又、使用の一態様として、
3成分を混合、加熱して注型し、これを冷却固化
し成型品としたものを溶融して塗布することもで
きる。
さらに本発明の組成物にワツクスの耐候性を向
上させるために酸化防止剤、紫外線防止剤、メツ
キ部分の防錆性を向上するために防錆添加剤を添
加することも効果的である。
本発明の保護膜を除去する方法としては、手拭
き、機械的洗浄方法等が考えられるが温水クリー
ナー(湯温65〜75℃噴出圧50〜80Kg/cm2、噴出量
500〜1500/h)で除去するのが適当である。本
組成物は水に不溶の成分のみで構成されているた
め温水クリーナーの洗浄廃液は砂ロ過装置を通す
だけで良い。またスチームケロシンや洗剤を含む
洗浄装置でも除去出来るが、複雑な廃液処理装置
が必要となるために不適当である。参考として記
すならば、ワツクスのみを塗布する場合にはスチ
ームケロシン・クリーナーが使用されている。
以下実施例について説明する。
実施例 1
(1) 下記組成物を50℃に加温して高速ミキサーで
十分に混合したもの500c.c.を小型乗用車にエア
レススプレーにて塗布し3ケ月間屋外に放置し
た後温水クリーナー(湯温65〜75℃、噴出圧70
Kg/cm2噴出水量600/h)で洗浄した。洗浄所
要時間約10分。洗浄後の塗装面、メツキ部分に
異状は認められず3ケ月前の状態を維持してい
た。
(2) 同じ組成物をアミノアルキツド塗装した塗装
板(450×600×1mm)に(1)と同じ方法で塗布し
(A)鳥の集まる木の近く(B)粉塵の立ちやすい所に
3ケ月間放置した後温水クリーナー((1)と同
じ)で洗浄した後、(A)鳥糞の落ちた部分の塗膜
の変化(B)粉塵の塗膜への付着について調べたが
いずれも異状が認められなかつた。
同時に本組成物を塗布せずに放置した塗装板
は鳥糞の落ちた部分に黄色のしみが認められ
た。また、粉塵中の鉄粉と思われる赤褐色の斑
点が認められた。
組成物 重量
セミマイクロクリスタリンワツクス(M.P.60
℃) 20重量部
沈澱性炭酸カルシウム 10〃
TFE重合体オリゴマー(粒径平均10μ、重合
度平均500) 10〃
ミネラルスピリツト 60重量部
(3) 同じ組成物を洗浄した軟鋼板(SPC70×150
×1mm)に(1)と同じ方法で塗布し屋外に3ケ月
間放置した後温水クリーナー((1)と同じ)で洗
浄した後、軟鋼板上の発錆状態を調べたが、発
錆は認められなかつた。同時に本組成物を塗布
せずに放置した軟鋼板は全面に発錆が認められ
た。
実施例1〜8、比較例1〜7の組成およびその
試験結果を表2に示す。[Table] To explain in more detail, the most important point of the present invention is that the wax contains a TFE polymer. Conventionally, it has been considered to incorporate powders of various organic and inorganic substances into the wax in order to improve the removability of the wax coating method, but since it is necessary to contain a large amount of powder, the wax coating method has been considered. The excellent protection properties of the material are lost, and the protection properties against permeable substances such as rust and bird droppings are reduced by half or almost non-existent. Furthermore, no improvement in removability was observed when a small amount of powder was added to the wax. As a result of various studies aimed at improving this point, the present inventors found that by incorporating a TFE polymer into the wax as in the present invention, it is possible to create a composition that has both excellent protective ability and easy removability. I found it.
There are many types of TFE polymers, ranging from liquids to solids, depending on the degree of polymerization.
It is called TFE wax and has a powdery appearance, but when it is evenly pressed onto a metal or painted surface, it has wax-like properties and is suitable as a TFE polymer. When a conventionally used high-molecular-weight TFE polymer powder was used instead of the TFE polymer in the present invention (Comparative Example 6), an effect on water repellency was observed; Character does not improve. On the other hand, when using TFE polymer (Examples 1 and 2), chemical resistance,
It has remarkable effects of imparting non-stick properties, water repellency, oil repellency, etc.
It also has excellent removability. Furthermore, if ethylene or propylene polymer powders having a relatively low molecular weight are used, they will dissolve in the wax due to their compatibility with the wax, and no removability effect can be expected. The present invention is characterized by the discovery that TFE polymer has unique properties not found in general inorganic materials, organic polymers, and oligomers, and the addition of this to wax.
or more, insoluble or poorly soluble in water, and particle size
The present invention maintains excellent protective properties as a surface protective agent that could not be obtained conventionally by adding organic and/or inorganic powders of 100μ or less in size, and also has easy removability when no longer needed. The product was obtained. The mixing ratio of each component in the composition of the present invention is determined depending on the required degree of protective ability and required degree of removability, but generally the wax is 2 to 98 parts by weight, has a melting point of 100°C or higher, is insoluble in water, or has a melting point of 100°C or higher. It is necessary to use 1 to 49 parts by weight of an organic and/or inorganic powder that is poorly soluble and has a particle size of 100 μm or less, and 1 to 49 parts by weight of the TFE polymer. If the wax is not contained in an amount of at least 2 parts by weight, the formation of a continuous protective film will be insufficient and the protective ability will be reduced. Moreover, if it exceeds 98 parts by weight, the performance will be the same as that of wax alone, making it difficult to remove. If at least 1 part by weight or more of organic and/or inorganic powder with a melting point of 100°C or higher, insoluble or poorly soluble in water, and a particle size of 100μ or less is not included, only the wax-like properties of the TFE polymer will appear and the removability will deteriorate. No improvement observed. When the content is 49 parts by weight or more, it becomes easy to peel off and the protective ability is extremely reduced. If the TFE polymer does not contain at least 1 part by weight, chemical resistance, non-adhesiveness, water repellency, and oil repellency will not be imparted. If it contains 49 parts by weight or more, TFE
The powdery nature of the polymer becomes strong and it becomes easy to peel off, reducing its protective ability. Waxes that can be used in the present invention include various mineral waxes, animal and vegetable waxes, hydrogenated oils and fats, synthetic waxes, etc. alone or in mixtures, but waxes with a melting point of about 40 to 90°C are preferred for ease of removal, and more preferably It is a semi-microcrystalline wax with a temperature of 50-70℃. Organic and/or inorganic powders include:
It needs to be in a powder form because it coexists with the TFE polymer and works together to maintain the protective properties of the protective film while making it brittle and easy to peel off. must be insoluble or poorly soluble in water at temperatures above 100°C and have a particle size of 100μ or less. These conditions, such as heating, are necessary when using the composition, and if the particle size is larger than the above, the protective ability will be insufficient. Further, it is necessary that it is insoluble in the dispersion medium used for coating.
Examples include organic powders such as powders of polymer compounds such as nylon, polyethylene, and phenolic resins; and calcium carbonate, talc, silicic anhydride, bentonite, and ummo as inorganic powders. Calcium carbonate, talc, and bentonite are suitable from the viewpoint of price and availability. TFE polymer is generally referred to as TFE wax and has a molecular weight of about 100,000 or less.
A powder that has a molecular weight of about 1000 or more, and can be produced by telomerization, thermal decomposition, radiolysis, etc., but from the viewpoint of dispersibility, the particle size should be 50 μm.
Below, preferably 20μ or less. From the viewpoint of workability, it is preferable to apply the composition of the present invention to the surface to be protected by dissolving and suspending it in a volatile solvent. The volatile solvent should be determined depending on the condition (material) of the surface to be applied, and should not attack these surfaces. Aliphatic hydrocarbon solvents are generally preferred. The amount of solvent to be used should be determined depending on the coating conditions, but if it is too small, gelation will occur, so it is necessary to use at least 100 parts by weight per 100 parts by weight of the above mixture. Furthermore, the use of a large amount of solvent is disadvantageous from the economical and pollution standpoints. Therefore, it is desirable that the amount is about 100 to 300 parts by weight per 100 parts by weight of the above mixture. In addition, as one mode of use,
It is also possible to mix the three components, heat them, cast them, cool and solidify them to form a molded product, which is then melted and applied. Furthermore, it is also effective to add an antioxidant and an ultraviolet ray inhibitor to the composition of the present invention to improve the weather resistance of the wax, and an anti-rust additive to improve the rust-preventing property of the plating part. Possible methods for removing the protective film of the present invention include manual wiping, mechanical cleaning, etc., but hot water cleaner (hot water temperature 65-75℃, jetting pressure 50-80 kg/cm 2 , jetting amount
500 to 1500/h) is appropriate. Since this composition is composed only of water-insoluble components, the cleaning waste liquid from the hot water cleaner only needs to be passed through a sand filtration device. It can also be removed using a cleaning device containing steam kerosene or detergent, but this is not suitable because it requires a complicated waste liquid treatment device. For reference, when applying only wax, a steam kerosene cleaner is used. Examples will be described below. Example 1 (1) 500 c.c. of the following composition was heated to 50°C and thoroughly mixed with a high-speed mixer, and applied to a small passenger car using an airless sprayer. After leaving it outdoors for 3 months, it was heated with a hot water cleaner ( Water temperature 65-75℃, jet pressure 70
Kg/cm 2 water jet amount 600/h). Cleaning time required: approximately 10 minutes. After cleaning, no abnormalities were observed on the painted surface or plating area, which remained in the same condition as three months ago. (2) Apply the same composition to a painted board (450 x 600 x 1 mm) coated with amino alkyd using the same method as in (1).
(A) Near a tree where birds gather (B) After being left in a dusty place for 3 months and then cleaned with a hot water cleaner (same as (1)), (A) Paint film on the area where bird droppings have fallen. Change in (B) The adhesion of dust to the paint film was investigated, but no abnormality was observed. At the same time, yellow stains were observed in the areas where bird droppings had fallen on painted boards that had been left without applying this composition. In addition, reddish-brown spots that appeared to be iron powder in the dust were observed. Composition Weight semi-microcrystalline wax (MP60
°C) 20 parts by weight Precipitated calcium carbonate 10〃 TFE polymer oligomer (average particle size 10μ, average degree of polymerization 500) 10〃 Mineral spirits 60 parts by weight (3) Mild steel plate washed with the same composition (SPC70×150
x 1mm) using the same method as in (1), left it outdoors for 3 months, washed it with a hot water cleaner (same as in (1)), and then examined the state of rust on the mild steel plate. It wasn't recognized. At the same time, rust was observed on the entire surface of the mild steel plate that was left without being coated with this composition. The compositions and test results of Examples 1 to 8 and Comparative Examples 1 to 7 are shown in Table 2.
【表】【table】
【表】
以上の結果かもわかるように本発明はワツク
ス、四弗化エチレンオリゴマー、有機物および/
または無機物の粉末を特定の範囲で使用すること
により、従来より検討されていた方法に比べて保
護性、除去性ともにすぐれていることが明白であ
る。[Table] As can be seen from the above results, the present invention is effective for wax, tetrafluoroethylene oligomer, organic matter and/or
It is clear that the use of inorganic powder in a specific range provides superior protection and removability compared to conventional methods.
Claims (1)
末 1〜49重量部、 c 融点が100℃以上で水に不溶性または難溶性
でかつ粒子径100μ以下の有機物及び/または
無機物の粉末 1〜49重量部 を含むことを特徴とする物品の表面保護剤組成
物。 2 四弗化エチレン重合体粉末が四弗化エチレン
ワツクスの粉末である特許請求の範囲第1項の組
成物。 3 ワツクスが融点60℃のセミマイクロクリスタ
リンワツクスである特許請求の範囲第1項の組成
物。 4 有機物及び/または無機物の粉末が炭酸カル
シウムの微粉末である特許請求の範囲第1項の組
成物。[Scope of Claims] 1 a Wax 2 to 98 parts by weight, b Tetrafluoroethylene polymer powder having a molecular weight of 100,000 or less 1 to 49 parts by weight, c Melting point of 100°C or higher, insoluble or sparingly soluble in water, and particle size A surface protective agent composition for an article, comprising 1 to 49 parts by weight of organic and/or inorganic powder having a size of 100 μm or less. 2. The composition according to claim 1, wherein the tetrafluoroethylene polymer powder is a tetrafluoroethylene wax powder. 3. The composition according to claim 1, wherein the wax is a semi-microcrystalline wax with a melting point of 60°C. 4. The composition according to claim 1, wherein the organic and/or inorganic powder is a fine powder of calcium carbonate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13642477A JPS5469584A (en) | 1977-11-14 | 1977-11-14 | Product surfact protecting agent composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13642477A JPS5469584A (en) | 1977-11-14 | 1977-11-14 | Product surfact protecting agent composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5469584A JPS5469584A (en) | 1979-06-04 |
| JPS6158507B2 true JPS6158507B2 (en) | 1986-12-11 |
Family
ID=15174818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13642477A Granted JPS5469584A (en) | 1977-11-14 | 1977-11-14 | Product surfact protecting agent composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5469584A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6344009U (en) * | 1986-09-10 | 1988-03-24 |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6260236U (en) * | 1985-09-30 | 1987-04-14 | ||
| JPH0613663B2 (en) * | 1987-08-04 | 1994-02-23 | 株式会社ウイルソン | Coating treatment agent for painted surface |
| TW575949B (en) | 2001-02-06 | 2004-02-11 | Hitachi Ltd | Mixed integrated circuit device, its manufacturing method and electronic apparatus |
| JP6916493B2 (en) * | 2016-04-12 | 2021-08-11 | ダイキン工業株式会社 | A coating film, a composition for a coating film, a film-forming agent, an article having a coating film, and a coating film forming method. |
| JP6384843B2 (en) * | 2017-08-21 | 2018-09-05 | 国立大学法人弘前大学 | Fluorine-containing nanocomposite particles and method for producing the same, coating agent containing the same, oil-water separation membrane, and resin composition |
-
1977
- 1977-11-14 JP JP13642477A patent/JPS5469584A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6344009U (en) * | 1986-09-10 | 1988-03-24 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5469584A (en) | 1979-06-04 |
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