JPH10237389A - Glazing agent of leather shoes - Google Patents

Glazing agent of leather shoes

Info

Publication number
JPH10237389A
JPH10237389A JP9060025A JP6002597A JPH10237389A JP H10237389 A JPH10237389 A JP H10237389A JP 9060025 A JP9060025 A JP 9060025A JP 6002597 A JP6002597 A JP 6002597A JP H10237389 A JPH10237389 A JP H10237389A
Authority
JP
Japan
Prior art keywords
wax
leather shoes
perfluoroalkyl group
polymer
group
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
Application number
JP9060025A
Other languages
Japanese (ja)
Inventor
Shigeki Akimitsu
茂喜 秋満
Kengo Maruishi
健悟 丸石
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MoonStar Co
Original Assignee
MoonStar Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by MoonStar Co filed Critical MoonStar Co
Priority to JP9060025A priority Critical patent/JPH10237389A/en
Publication of JPH10237389A publication Critical patent/JPH10237389A/en
Pending legal-status Critical Current

Links

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  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the subject glazing agent capable of expressing stainproof properties against stains caused by mud water and oils by containing a polymer having a specific group in side chains. SOLUTION: This glazing agent contains (B) a polymer having perfluoroalkyl groups in side chains [preferably a polymer having a structure shown by figure (A is a polar group; B is a bonded group)] in (A) a wax (preferably a wax having >=60 deg.C melting point measured by JIS K-2235, e.g. carnauba wax, montan wax, microcrystalline wax, etc.). The perfluoroalkyl group in the ingredient B is preferably a >=7C straight chain. When a coated material with the glazing agent is a leather, it is preferable to use a copolymer of (meth)acrylic acid having the perfluoroalkyl group.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は革靴の仕上げ工程の
最終工程ポリッシングや靴磨きに用いられる艶出し剤に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polishing agent used in polishing and polishing of shoes in the final step of finishing leather shoes.

【0002】[0002]

【従来の技術】従来の革靴の仕上げ工程での目潰しやポ
リッシングに使用する艶出し剤として、カルナバワック
スなどの植物系天然ワックス,モンタンワックスなどの
鉱物系ワックス,マイクロクリスタリンワックスなどの
石油系天然ワックス,モンタンワックスをベースとする
合成エステルワックス等のワックス類が使用されてい
る。又、靴磨きにはこれらのワックス類に油と水とを加
えた乳化性クリームも使用されている。
2. Description of the Related Art As a polishing agent used for crushing and polishing in a conventional leather shoe finishing process, a vegetable-based natural wax such as carnauba wax, a mineral-based wax such as montan wax, and a petroleum-based natural wax such as microcrystalline wax. And waxes such as synthetic ester waxes based on montan wax. For shoe polishing, emulsifying creams obtained by adding oil and water to these waxes are also used.

【0003】[0003]

【発明が解決しようとする課題】これらの艶出し剤は天
然皮革に対して優れた艶を与え、ある程度撥水性もあ
り、皮革を保護する役目も果たしているが、油性の汚れ
に対しては弱く、一度油がしみこむと取り去ることがで
きず、油性の汚れに対して保護する効果が全くなかっ
た。本発明は泥水や油性の汚れに対して防汚性を有する
艶出し剤を提供することにより、艶出し効果に加えて防
汚性をも付与した革靴を得ることを課題とするものであ
る。
These polishes provide excellent luster to natural leather, have some water repellency, and also serve to protect leather, but are weak against oily stains. Once the oil had soaked, it could not be removed and had no protective effect against oily stains. An object of the present invention is to provide a polisher having antifouling properties against muddy water and oily dirt, thereby obtaining leather shoes having an antifouling property in addition to the polisher effect.

【0004】[0004]

【課題を解決するための手段】本発明の革靴用艶出し剤
は、ワックスにパーフルオロアルキル基を側鎖に有する
ポリマーを含むことを第1の特徴とする。又、本発明の
革靴用艶出し剤は、JIS K−2235で測定した融
点が60℃以上のワックスにパーフルオロアルキル基を
側鎖に有するアクリル酸共重合体を含むことを第2の特
徴とする。
The first feature of the polishing agent for leather shoes of the present invention is that the wax contains a polymer having a perfluoroalkyl group in a side chain. The second feature of the polishing agent for leather shoes of the present invention is that a wax having a melting point of 60 ° C. or higher as measured by JIS K-2235 contains an acrylic acid copolymer having a perfluoroalkyl group in a side chain. I do.

【0005】本発明の革靴用艶出し剤において、必須成
分として用いられるワックスとしては、例えばカルナバ
ワックス,キャンテリラワックス,シュガーワックス,
ライスワックス,木ロウ,ベイベリーワックス,オーキ
ュリーワックス,エスパルトワックスなどの植物系天然
ワックス,ミツロウ,こん虫ロウ,鯨ロウ,セラックロ
ウ,ラノリンワックスなどの動物系天然ワックス,パラ
フィンワックス,マイクロクリスタリンワックスなどの
石油系天然ワックス,モンタンワックス,オゾケライト
ワックス,セレシンなどの鉱物系天然ワックス,ヘキス
トワックス,ポリエチレンワックス,カルボワックス,
カスターワックス,フィッシャトロプッシュワックス,
サゾールワックスなどの合成ワックスが挙げられる。
The wax used as an essential component in the polishing agent for leather shoes of the present invention includes, for example, carnauba wax, canterilla wax, sugar wax,
Vegetable natural waxes such as rice wax, wood wax, bayberry wax, ocully wax, espart wax, animal natural waxes such as beeswax, insect wax, whale wax, shellac wax, lanolin wax, paraffin wax, microcrystalline wax Mineral waxes such as petroleum natural wax, montan wax, ozokerite wax, ceresin, etc., Hoechst wax, polyethylene wax, carbowax,
Caster wax, fishertro push wax,
Synthetic waxes such as Sasol wax are exemplified.

【0005】これらのワックスの中で、特に好ましいの
はJIS K−2235で測定した融点が60℃以上の
カルナバワックス,モンタンワックス,マイクロクリス
タリンワックス,セラックロウパラフィンワックス,合
成エステルワックスの中から選ばれる少なくとも1つで
ある。
Among these waxes, particularly preferred are those selected from carnauba wax, montan wax, microcrystalline wax, shellac wax paraffin wax, and synthetic ester wax having a melting point of 60 ° C. or higher as measured by JIS K-2235. At least one.

【0006】前記ワックスはそれぞれ単独で用いても良
いし、2種以上組み合わせて使用しても良い。JIS
K−2235で測定した融点が60℃以上のワックスを
革靴用仕上げ剤として用いれば革の表面に厚くて丈夫な
ワックス被膜を作ることができ、傷や汚れに対して強
い。
The above waxes may be used alone or in combination of two or more. JIS
If a wax having a melting point of 60 ° C. or higher as measured by K-2235 is used as a finishing agent for leather shoes, a thick and durable wax film can be formed on the surface of the leather, and is resistant to scratches and stains.

【0007】本発明の革靴用艶出し剤には、撥水,撥油
性を付与するためにパーフルオロアルキル基を側鎖に有
するポリマーを使用する。パーフルオロアルキル基を有
するポリマーを固体表面に被覆すると、表面エネルギー
は著しく低くなり、高度の撥水,撥油性を示すようにな
る。パーフルオロアルキル基を有するポリマーの構造
は、図1に示すようなポリマー主鎖の側鎖に極性基や結
合基を介してパーフルオロアルキル基が結合されている
構造を有するのが好ましいとされている。
As the polishing agent for leather shoes of the present invention, a polymer having a perfluoroalkyl group in a side chain is used for imparting water repellency and oil repellency. When a polymer having a perfluoroalkyl group is coated on a solid surface, the surface energy is remarkably reduced, and the solid surface exhibits high water and oil repellency. It is considered that the structure of the polymer having a perfluoroalkyl group preferably has a structure in which a perfluoroalkyl group is bonded to a side chain of a polymer main chain via a polar group or a bonding group as shown in FIG. I have.

【0008】図1のAは、被処理物に対する親和性を与
え、又、有機溶剤などへの溶解性を増すための極性基で
あり、Bはこの極性基とパーフルオロアルキル基を結ぶ
ために必要な結合基である。その結合基Bとしては−S
2 N(R)(CH2 )m −か−CH2 −或いは−CH
2 CH2 −が用いられる。又、パーフルオロアルキル基
の長さは重要であり、低エネルギー表面を効果的に形成
するように炭素数が7以上の直鎖のパーフルオロアルキ
ル基が使用される。前記のパーフルオロアルキル基をも
つポリマーは撥水性だけでなく、通常の炭化水素に対す
る撥油性も発揮するようになる。
FIG. 1A shows a polar group for imparting an affinity to an object to be treated and increasing the solubility in an organic solvent and the like, and B shows a polar group for connecting this polar group to a perfluoroalkyl group. It is a necessary linking group. The bonding group B is -S
O 2 N (R) (CH 2) m - or -CH 2 - or -CH
2 CH 2 -is used. The length of the perfluoroalkyl group is important, and a linear perfluoroalkyl group having 7 or more carbon atoms is used so as to effectively form a low energy surface. The polymer having a perfluoroalkyl group exhibits not only water repellency but also oil repellency to ordinary hydrocarbons.

【0009】被覆物が皮革である場合には、パーフルオ
ロアルキル基を有するアクリル酸の共重合体かメタクリ
ル酸の共重合体が使用される。そのうちでもアクリル酸
の共重合体は屈曲性が大きいので動的な力が加わる革靴
用の艶出し剤として好ましい。
When the coating is leather, a copolymer of acrylic acid or methacrylic acid having a perfluoroalkyl group is used. Among them, the copolymer of acrylic acid is preferable as a polishing agent for leather shoes to which a dynamic force is applied because of its great flexibility.

【0010】本発明の革靴用の艶出し剤を製造する場
合、ワックスにパーフルオロアルキル基を有するポリマ
ーを混合するが、混合の方法としてワックスを加熱溶融
して、その中に前記ポリマーをエマルジョンにしたもの
を攪拌して、水分を蒸発しながら混合すると良い。
When the polishing agent for leather shoes of the present invention is produced, a polymer having a perfluoroalkyl group is mixed with wax. As a mixing method, the wax is heated and melted, and the polymer is formed into an emulsion therein. It is advisable to stir and mix while evaporating the water.

【0011】このようにして混合された艶出し剤は、型
の中に流し込み、冷却して固形状物に加工される。本発
明の革靴用艶出し剤は、起毛布を多数積層した研磨布を
回転機に取り付けた研磨機の起毛面に塗布された後、革
靴の革の表面をこの研磨機で磨くことにより塗布され
る。
The polishing agent mixed in this way is poured into a mold, cooled and processed into a solid. The polishing agent for leather shoes of the present invention is applied to the raised surface of a polishing machine in which a plurality of brushed cloths are stacked on a rotating machine, and then applied by polishing the leather surface of the shoe with this polishing machine. You.

【0012】本発明の艶出し剤において、パーフルオロ
アルキル基を側鎖に有するアクリル酸の共重合体を使用
した場合、塗布後、加熱することにより革に強固に密着
し、加熱前に比べ撥水性や撥油性が増す。
In the polishing agent of the present invention, when a copolymer of acrylic acid having a perfluoroalkyl group in the side chain is used, it is firmly adhered to leather by heating after application, and is repellent compared to before heating. Increases water and oil repellency.

【0013】[0013]

【実施例】【Example】

【艶出し剤の製造】実施例に使用するワックスは、JI
S K−2235で測定した融点80〜86℃のカルナ
バワックスを用いる。又、パーフルオロアルキル基を有
するポリマーには炭素数8のパーフルオロアルキル基を
側鎖に有するアクリル酸エチルの共重合体をエマルジョ
ンした共栄社化学株式会社製,商品名ライトガードFR
520(固形分24%)を使用する。カルナバワックス
を所定量計量し、容器の中で100℃前後に加熱,溶融
させ、前記エマルジョンを同重量部混合し、水分を加熱
蒸発させた後、型に流し込み自然冷却させ、型から抜
き、実施例の艶出し剤を製造した。この艶出し剤の配合
は表1の通りである。
[Manufacture of polishing agent] The wax used in the examples is JI
Carnauba wax having a melting point of 80 to 86 ° C. measured by SK-2235 is used. Further, the polymer having a perfluoroalkyl group is a light guard FR (trade name, manufactured by Kyoeisha Chemical Co., Ltd.) prepared by emulsifying a copolymer of ethyl acrylate having a perfluoroalkyl group having 8 carbon atoms in the side chain.
520 (24% solids) is used. A predetermined amount of carnauba wax is weighed, heated and melted at about 100 ° C. in a container, mixed with the same weight part of the emulsion, heated and evaporated, poured into a mold, allowed to cool naturally, and removed from the mold. Example polishes were prepared. Table 1 shows the composition of the polishing agent.

【0014】[0014]

【表1】 [Table 1]

【0015】[0015]

【実施例の艶出し剤で仕上げした革靴】この艶出し剤を
起毛布を、多数積層して研磨材とした研磨機に擦りつ
け、仕上げ後の革靴をこの研磨機で目潰し、ポリッシン
グした。さらに革靴の120℃で1分加熱した後、再度
研磨機にてポリッシングを行い、実施例の革靴を得た。
Leather shoes finished with the glazing agent of the examples: A large number of brushed cloths were rubbed with a polisher as an abrasive, and the finished leather shoes were crushed and polished with the polisher. Further, after the leather shoes were heated at 120 ° C. for 1 minute, polishing was performed again with a polishing machine to obtain leather shoes of the examples.

【0016】[0016]

【比較例の艶出し剤で仕上げした革靴】比較例として、
カルナバワックスのみを別の研磨機に擦りつけ、仕上後
の別の革靴をこの研磨機で目潰し、ポリッシングを行
い、比較例の革靴を得た。
[Leather shoes finished with the polishing agent of the comparative example] As a comparative example,
Only carnauba wax was rubbed against another polishing machine, and another finished leather shoe was crushed with this polishing machine and polished to obtain a leather shoe of a comparative example.

【0017】[0017]

【実施例と比較例の革靴の性能比較】実施例と比較例の
革靴とを外観,撥水性,撥油性の3項目について比較を
行い表2に示した。表2より本発明の艶出し剤で革靴を
仕上げすることにより油性の汚れに対しても防汚性のあ
る革靴が得られた。
Performance Comparison of Leather Shoes of Example and Comparative Example Table 2 shows a comparison of the appearance, water repellency and oil repellency of the leather shoes of the example and the comparative example. As shown in Table 2, by finishing leather shoes with the polishing agent of the present invention, leather shoes having antifouling properties against oily stains were obtained.

【0018】[0018]

【表2】 ここで*1はJIS L1092スプレー法による。*
2はAATCC No,118 撥油性試験法による。
[Table 2] Here, * 1 is based on JIS L1092 spray method. *
2 is based on AATCC No. 118 oil repellency test method.

【0019】[0019]

【発明の効果】本発明の革靴用艶出し剤を用いて革靴の
目潰し、ポリッシングを行なうと、優れた艶感が得られ
ると共に、水や油に対して防汚性のある革靴に仕上げる
ことができた。
When the leather shoes are crushed and polished using the polishing agent for leather shoes of the present invention, an excellent luster can be obtained and the leather shoes can be finished to have antifouling properties against water and oil. did it.

─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成9年4月24日[Submission date] April 24, 1997

【手続補正2】[Procedure amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】図面の簡単な説明[Correction target item name] Brief description of drawings

【補正方法】追加[Correction method] Added

【補正内容】[Correction contents]

【図面の簡単な説明】[Brief description of the drawings]

【図1】 パーフルオロアルキル基含有化合物を固体表
面に処理した概念図である。
FIG. 1 is a conceptual diagram in which a perfluoroalkyl group-containing compound is treated on a solid surface.

【符号の説明】 A.極性基 B.結合基[Explanation of Codes] Polar group B. Linking group

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 ワックスにパーフルオロアルキル基を側
鎖に有するポリマーを含むことを特徴とする革靴用艶出
し剤。
1. A polishing agent for leather shoes, wherein the wax contains a polymer having a perfluoroalkyl group in a side chain.
【請求項2】 JIS K−2235で測定した融点が
60℃以上のワックスにパーフルオロアルキル基を側鎖
に有するアクリル酸共重合体を含むことを特徴とする革
靴用艶出し剤。
2. A polishing agent for leather shoes, wherein a wax having a melting point of 60 ° C. or higher as measured by JIS K-2235 contains an acrylic acid copolymer having a perfluoroalkyl group in a side chain.
【請求項3】 JIS K−2235で測定した融点が
60℃以上のワックスがカルナバワックス,モンタンワ
ックス,マイクロクリスタリンワックス,セラックロ
ウ,パラフィンワックス,合成エステルワックスの中か
ら選ばれた少なくとも1種である請求項2記載の革靴用
艶出し剤。
3. The wax having a melting point of at least 60 ° C. measured according to JIS K-2235 is at least one selected from carnauba wax, montan wax, microcrystalline wax, shellac wax, paraffin wax and synthetic ester wax. Item 4. A polishing agent for leather shoes according to Item 2.
【請求項4】 パーフルオロアルキル基が炭素数7以上
の直鎖のパーフルオロアルキル基である請求項1又は2
記載の革靴用艶出し剤。
4. The method according to claim 1, wherein the perfluoroalkyl group is a linear perfluoroalkyl group having 7 or more carbon atoms.
A glazing agent for leather shoes as described.
JP9060025A 1997-02-26 1997-02-26 Glazing agent of leather shoes Pending JPH10237389A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9060025A JPH10237389A (en) 1997-02-26 1997-02-26 Glazing agent of leather shoes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9060025A JPH10237389A (en) 1997-02-26 1997-02-26 Glazing agent of leather shoes

Publications (1)

Publication Number Publication Date
JPH10237389A true JPH10237389A (en) 1998-09-08

Family

ID=13130127

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9060025A Pending JPH10237389A (en) 1997-02-26 1997-02-26 Glazing agent of leather shoes

Country Status (1)

Country Link
JP (1) JPH10237389A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1149922A1 (en) * 2000-04-25 2001-10-31 Granger's International Ltd. Leather treatment
CN1309794C (en) * 2005-04-18 2007-04-11 蒋发学 Preservative agent for shining leather and stone
JP2011144380A (en) * 2003-07-29 2011-07-28 Three M Innovative Properties Co Composition, wipe and method for cleaning base material, protecting base material and glossing base material

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6390588A (en) * 1986-10-06 1988-04-21 Daikin Ind Ltd Water and oil repellent
JPS6399285A (en) * 1986-05-28 1988-04-30 Daikin Ind Ltd Water and oil repellent
JPH021795A (en) * 1988-03-08 1990-01-08 Asahi Glass Co Ltd Water and oil repellent
JPH06322213A (en) * 1993-05-11 1994-11-22 Asahi Glass Co Ltd Water-repellent oil-repellent composition and article coated therewith
JPH0931415A (en) * 1995-07-24 1997-02-04 Koronbusu:Kk Waterproof shoe cream manufacturing method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6399285A (en) * 1986-05-28 1988-04-30 Daikin Ind Ltd Water and oil repellent
JPS6390588A (en) * 1986-10-06 1988-04-21 Daikin Ind Ltd Water and oil repellent
JPH021795A (en) * 1988-03-08 1990-01-08 Asahi Glass Co Ltd Water and oil repellent
JPH06322213A (en) * 1993-05-11 1994-11-22 Asahi Glass Co Ltd Water-repellent oil-repellent composition and article coated therewith
JPH0931415A (en) * 1995-07-24 1997-02-04 Koronbusu:Kk Waterproof shoe cream manufacturing method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1149922A1 (en) * 2000-04-25 2001-10-31 Granger's International Ltd. Leather treatment
JP2011144380A (en) * 2003-07-29 2011-07-28 Three M Innovative Properties Co Composition, wipe and method for cleaning base material, protecting base material and glossing base material
CN1309794C (en) * 2005-04-18 2007-04-11 蒋发学 Preservative agent for shining leather and stone

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