JPH07207197A - Resin composition for electrostatic coating - Google Patents

Resin composition for electrostatic coating

Info

Publication number
JPH07207197A
JPH07207197A JP1784794A JP1784794A JPH07207197A JP H07207197 A JPH07207197 A JP H07207197A JP 1784794 A JP1784794 A JP 1784794A JP 1784794 A JP1784794 A JP 1784794A JP H07207197 A JPH07207197 A JP H07207197A
Authority
JP
Japan
Prior art keywords
coating
powder
resin
vinyl chloride
resin 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.)
Pending
Application number
JP1784794A
Other languages
Japanese (ja)
Inventor
Yoshitaka Ito
義孝 伊藤
Kazuki Takagi
一樹 高木
Yoshito Fujiki
芳人 藤木
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.)
Toagosei Co Ltd
Original Assignee
Toagosei Co Ltd
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 Toagosei Co Ltd filed Critical Toagosei Co Ltd
Priority to JP1784794A priority Critical patent/JPH07207197A/en
Publication of JPH07207197A publication Critical patent/JPH07207197A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a resin composition for electrostatic coating prepared by mixing a specific salicylic compound into powder of a thermoplastic resin, and suitable for the frictional charging process because of its large frictional charge capacity. CONSTITUTION:The composition is prepared by mixing powder of thermoplastic resin such as polyethylene, polypropylene, nylon, or vinyl chloride resin with an alkaline earth metal salt of (alkyl) salicyclic acid, preferably in an amount of 0.05 to 10wt.% base on the total weight of the composition.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、熱可塑性樹脂粉末を主
成分とする静電塗装用樹脂粉体組成物に関するものであ
り、さらに詳しくは、摩擦帯電方式の静電粉体塗装機に
よる塗装に特に適した粉体塗装用熱可塑性樹脂組成物に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin powder composition for electrostatic coating containing a thermoplastic resin powder as a main component, and more specifically, coating with a triboelectric electrostatic powder coating machine. Particularly, it relates to a thermoplastic resin composition for powder coating.

【0002】[0002]

【従来の技術】粉体塗料は、溶剤型塗料に比べ、溶剤を
使用しないことに由来する多くの利点を有しており、塗
装機械の進歩と相まって、近年急速に需要が拡大してい
る。ポリエチレン、ポリプロピレン、ナイロンおよび塩
化ビニル系樹脂などの熱可塑性樹脂を主成分とする粉体
塗料の塗装方法に関しては、従来流動浸漬塗装法が一般
的に採用されてきたが、最近、塗装膜厚の管理や粉替え
が容易であることおよびエネルギーコストが少ないこと
等の理由から、主にコロナ放電方式による静電塗装法も
多用されるようになってきた。
2. Description of the Related Art Powder coating materials have many advantages over solvent-based coating materials because they do not use a solvent, and the demand for them has expanded rapidly in recent years due to the progress of coating machines. Regarding the coating method of powder coating material mainly composed of thermoplastic resin such as polyethylene, polypropylene, nylon and vinyl chloride resin, the fluidized dipping coating method has been generally adopted in the past. The electrostatic coating method based on the corona discharge method has come to be widely used mainly for reasons such as easy management and powder change and low energy cost.

【0003】他方静電塗装法には、上記コロナ放電方式
による静電塗装法以外に、摩擦帯電方式(トリボ帯電方
式)による静電塗装法があり、この静電塗装法は、高
電圧を使用していないので感電の危険性が少ない、電
界強度が弱いためコロナ帯電方式に比べて凹部への入り
込み性に優れる、また静電反発を起こし難いためより
平滑な塗面が得られる、等の特長を有しており、上記熱
可塑性樹脂への適用が望まれている。しかしながら、流
動浸漬塗装法やコロナ放電方式による静電塗装法におい
て採用された構成の熱可塑性樹脂粉体塗料は、摩擦帯電
方式による静電粉体塗装法では、帯電量が少な過ぎて使
用できないのが現状である。
On the other hand, as the electrostatic coating method, in addition to the electrostatic coating method by the corona discharge method, there is an electrostatic coating method by the friction charging method (tribo charging method). This electrostatic coating method uses a high voltage. Since it does not, there is less risk of electric shock, the electric field strength is weaker, it is easier to enter the recess than the corona charging method, and it is hard to cause electrostatic repulsion, so a smoother coated surface can be obtained. Therefore, application to the thermoplastic resin is desired. However, the thermoplastic resin powder coating composition adopted in the fluid immersion coating method or the electrostatic coating method using the corona discharge method cannot be used in the electrostatic powder coating method using the friction charging method because the charge amount is too small. Is the current situation.

【0004】[0004]

【課題を解決するための手段】本発明者等は、上記の課
題を解決するために鋭意検討した結果、サリチル酸又は
アルキルサルチル酸のアルカリ土金属塩を塩化ビニル系
樹脂粉末に混合して得られる樹脂組成物が、摩擦により
容易に高荷電量に帯電することを見出し、本発明を完成
するに至った。
Means for Solving the Problems As a result of intensive studies for solving the above problems, the present inventors have obtained a mixture of an alkaline earth metal salt of salicylic acid or alkylsalicylic acid with a vinyl chloride resin powder. The inventors have found that the resin composition is easily charged to a high charge amount by friction, and have completed the present invention.

【0005】即ち、本発明は、サリチル酸又はアルキル
サルチル酸のアルカリ土金属塩を熱可塑性樹脂の粉末に
混合してなる、摩擦帯電方式の静電粉体塗装用樹脂組成
物である。
That is, the present invention is a triboelectrification type electrostatic powder coating resin composition obtained by mixing an alkaline earth metal salt of salicylic acid or alkylsalicylic acid with a powder of a thermoplastic resin.

【0006】本発明におけるアルキルサルチル酸として
は、炭素数が5以下のアルキル基を1個または2個有す
るアルキルサルチル酸が好ましく、さらに好ましくは、
t−ブチル基等の炭素数が4以下のアルキル基を1個ま
たは2個有するアルキルサルチル酸であり、特に好まし
くは、t−ブチル基を2個有するものである。また、ア
ルカリ土金属としては、カルシウム、ストロンチウム、
バリウム、ベリリウムおよびマグネシウム等が挙げら
れ、好ましくは、ストロンチウム、バリウムおよびマグ
ネシウムである。
The alkylsalicylic acid in the present invention is preferably an alkylsalicylic acid having one or two alkyl groups having 5 or less carbon atoms, and more preferably
An alkylsalicylic acid having one or two alkyl groups having 4 or less carbon atoms such as a t-butyl group, and particularly preferably one having two t-butyl groups. Also, as alkaline earth metals, calcium, strontium,
Examples thereof include barium, beryllium and magnesium, and preferably strontium, barium and magnesium.

【0007】本発明においては、上記アルキルサルチル
酸又はサルチル酸とアルカリ土金属とからなる塩を熱可
塑性樹脂の粉末に配合するが、該金属塩の好ましい配合
量は、樹脂組成物全体に対して、0.05〜10重量%
である。0.05重量%未満では、所定の塗装性改良効
果が得られ難く、一方10重量%を超えると塗膜の平滑
性及び機械的特性の低下が起こり易い。
In the present invention, the salt of alkylsalicylic acid or salicylic acid and an alkaline earth metal is blended with the powder of the thermoplastic resin, and the preferred blending amount of the metal salt is based on the entire resin composition. , 0.05-10% by weight
Is. If it is less than 0.05% by weight, it is difficult to obtain a predetermined effect of improving the coating property, while if it exceeds 10% by weight, the smoothness and mechanical properties of the coating film tend to be deteriorated.

【0008】本発明における金属塩は、粉体塗装用組成
物中に均一に分散させる必要があるが、そのためには粒
子径が0.1〜20μmであることが好ましい。0.1
μm未満の場合、特に添加量が多い系では、塗面の平滑
性が低下し易く、一方20μmを超えると塗面にブツを
発生し易くなると共に、電荷調整効果が十分に発揮され
ず、摩擦帯電方式の静電粉体塗装機を使用した場合に於
ける塗装性の改良という初期の目的が達成できなくなる
恐れがある。金属塩の樹脂粉末への添加は、通常の粉体
塗料の生産工程に従い、樹脂の溶融混合時に添加するメ
ルトブレンド方式または生産工程の後半である樹脂の粉
砕時に添加するドライブレンド方式のいずれによっても
行うことができる。
The metal salt in the present invention is required to be uniformly dispersed in the powder coating composition, and for that purpose, the particle diameter is preferably 0.1 to 20 μm. 0.1
If it is less than μm, the smoothness of the coating surface is likely to be deteriorated especially in a system with a large amount of addition, while if it exceeds 20 μm, the coating surface is liable to be bumped and the charge adjusting effect is not sufficiently exerted, resulting in friction. There is a possibility that the initial purpose of improving the coatability when the electrostatic powder coating machine of the charging type is used cannot be achieved. The metal salt is added to the resin powder according to the usual powder coating production process, either by the melt blending method added during the melt mixing of the resin or the dry blending method added during the pulverization of the resin which is the latter half of the production process. It can be carried out.

【0009】本発明の粉体塗装用樹脂組成物における熱
可塑性樹脂としては、ポリエチレン、ポリプロピレン、
11−ナイロンおよび12−ナイロン等のナイロンおよ
び塩化ビニル系樹脂等が挙げられる。また、塩化ビニル
系樹脂としては、懸濁重合法によって得られる塩化ビニ
ル単独重合体および塩化ビニルと他のビニル単量体から
なる塩化ビニル系共重合体が使用でき、該共重合体の具
体例としては、酢酸ビニル−塩化ビニル共重合体、エチ
レン−塩化ビニル共重合体および塩化ビニリデン−塩化
ビニル共重合体等が挙げられる。
The thermoplastic resin in the resin composition for powder coating of the present invention includes polyethylene, polypropylene,
Nylon such as 11-nylon and 12-nylon, vinyl chloride resin and the like can be mentioned. Further, as the vinyl chloride resin, a vinyl chloride homopolymer obtained by a suspension polymerization method and a vinyl chloride copolymer composed of vinyl chloride and other vinyl monomers can be used. Specific examples of the copolymer Examples thereof include vinyl acetate-vinyl chloride copolymer, ethylene-vinyl chloride copolymer, vinylidene chloride-vinyl chloride copolymer and the like.

【0010】塩化ビニル系樹脂の好ましい重合度は60
0〜1100である。塩化ビニル系樹脂の重合度が、6
00未満であると塗膜の機械的強度および耐候性が不足
し易く、一方1100を越えると溶融性が不十分になる
ことがある。
The preferred degree of polymerization of vinyl chloride resin is 60.
It is 0-1100. The degree of polymerization of vinyl chloride resin is 6
If it is less than 00, the mechanical strength and weather resistance of the coating film tend to be insufficient, while if it exceeds 1100, the meltability may become insufficient.

【0011】上記熱可塑性樹脂組の粉末の平均粒径は、
10〜200μmの範囲が好ましい。平均粒径が10μ
m未満の場合は、粉体特性の低下が著しく、二次凝集や
ブロッキングを起こし易くなる。この結果、塗装機から
の樹脂の吐出量が不安定となり、連続塗装性が維持でき
ず、膜厚にばらつきが出やすくなると共に、塗装機の掃
除頻度が多くなるため、作業性が低下するという問題が
ある。一方平均粒径が200μmを超える場合は、塗着
効率が低下すると共に平滑な塗面が得られ難くなる恐れ
がある。
The average particle size of the above-mentioned thermoplastic resin powder is
The range of 10 to 200 μm is preferable. Average particle size is 10μ
When it is less than m, the powder properties are remarkably deteriorated, and secondary aggregation and blocking are likely to occur. As a result, the amount of resin discharged from the coater becomes unstable, continuous coatability cannot be maintained, film thickness tends to vary, and the coater must be cleaned more frequently, resulting in reduced workability. There's a problem. On the other hand, if the average particle size exceeds 200 μm, the coating efficiency may be reduced and it may be difficult to obtain a smooth coated surface.

【0012】上記熱可塑性樹脂の粉末およびサリチル酸
又はアルキルサルチル酸のアルカリ土金属塩を必須成分
とする、本発明の粉体塗装用樹脂組成物には、それら以
外に所望により顔料、可塑剤、充填剤、添加剤等を配合
することができる。また、熱可塑性樹脂として塩化ビニ
ル系樹脂を使用する場合には、塩化ビニル系樹脂100
重量部当たり、30〜50重量部程度の可塑剤を併用す
ることが好ましい。
The powder coating resin composition of the present invention, which contains the powder of the above-mentioned thermoplastic resin and the alkaline earth metal salt of salicylic acid or alkylsalicylic acid as essential components, may optionally further contain a pigment, a plasticizer and a filler. Agents, additives and the like can be added. When a vinyl chloride resin is used as the thermoplastic resin, the vinyl chloride resin 100
It is preferable to use about 30 to 50 parts by weight of a plasticizer per part by weight.

【0013】[0013]

【実施例】以下、実施例及び比較例を挙げて本発明を更
に詳しく説明する。なお、以下に示す部数は重量部を表
す。 <実施例1〜3>重合度700で平均粒径30〜90μ
mの塩化ビニル樹脂〔東亞合成化学工業(株)製、商品
名TS−700M〕100部に対して、トリ−2−エチ
ルヘキシルトリメリテート40部、ジブチル錫メルカプ
ト7部、エポキシ化アマニ油3部および顔料として酸化
チタン5.0部を加熱ジャケット付きヘンシェルミキサ
ーに投入し、100〜150℃の温度で約20分間加熱
混合した。次いで、70℃以下に冷却した後、塩化ビニ
ルの乳化重合微粒体〔日本ゼオン(株)製、商品名Ge
on121〕を5部添加し、5分間撹拌を行い、最後に
以下に示す量のジ−t−ブチルサリチル酸バリウム塩を
それぞれ配合し、更に1分間撹拌を行った。
EXAMPLES The present invention will be described in more detail with reference to Examples and Comparative Examples. The number of parts shown below represents parts by weight. <Examples 1 to 3> Polymerization degree 700 and average particle size 30 to 90 μm
m vinyl chloride resin [manufactured by Toagosei Co., Ltd., trade name TS-700M] 100 parts, tri-2-ethylhexyl trimellitate 40 parts, dibutyltin mercapto 7 parts, epoxidized linseed oil 3 parts Then, 5.0 parts of titanium oxide as a pigment was charged into a Henschel mixer with a heating jacket, and heated and mixed at a temperature of 100 to 150 ° C. for about 20 minutes. Then, after cooling to 70 ° C. or lower, emulsion-polymerized fine particles of vinyl chloride [manufactured by Nippon Zeon Co., Ltd., trade name Ge
on121] was added, and the mixture was stirred for 5 minutes. Finally, the barium salt of di-t-butylsalicylic acid was added in the amounts shown below, and the mixture was further stirred for 1 minute.

【0014】 実施例1:ジ−t−ブチルサリチル酸バリウム塩 0.2部 実施例2: 〃 0.4部 実施例3: 〃 0.6部 上記操作によって得られた混合物を60メッシュの篩い
で分級し、塩化ビニル系樹脂の粉体塗装用樹脂組成物を
製造した。
Example 1: Barium di-t-butylsalicylate 0.2 parts Example 2: 〃 0.4 parts Example 3: 〃 0.6 parts The mixture obtained by the above operation is sieved with a 60 mesh sieve. Classification was carried out to produce a vinyl chloride resin powder coating resin composition.

【0015】上記実施例の粉体塗装用樹脂組成物を使用
して、静電塗装時の摩擦帯電特性を評価した。摩擦帯電
特性の評価は、松尾産業(株)製トリボ帯電方式静電塗
装機(商品名ザ・摩擦)を使用して、塗料吐出量を15
0g/分で、塗料を2分間連続して吐出した際の帯電量
(μA)に依った。本方法によって帯電量が2μA以上
のとき、実ラインでの連続塗装が可能である。評価結果
は以下のとおりである。 実施例1:トリボ帯電量(μA) 6.5 実施例2: 〃 7.0 実施例3: 〃 7.5
The resin composition for powder coating of the above example was used to evaluate the triboelectrification characteristics during electrostatic coating. The triboelectrification characteristics were evaluated by using a tribo electrostatic type electrostatic coating machine (trade name: The friction) manufactured by Matsuo Sangyo Co., Ltd.
It depended on the charge amount (μA) when the coating material was continuously discharged for 2 minutes at 0 g / min. By this method, continuous coating on an actual line is possible when the charge amount is 2 μA or more. The evaluation results are as follows. Example 1: Tribo charge amount (μA) 6.5 Example 2: 〃 7.0 Example 3: 〃 7.5

【0016】<実施例4〜5>実施例2におけるジ−t
−ブチルサリチル酸バリウム塩を、ジ−t−ブチルサリ
チル酸マグネシウム塩(実施例4)またはジ−t−ブチ
ルサリチル酸ストロンチウム塩(実施例5)に変更した
以外は、すべて実施例2と同様にして塩化ビニル系樹脂
の粉体塗装用樹脂組成物を製造した。上記塗装用樹脂組
成物についての摩擦帯電特性の評価結果は、以下のとお
りであった。 実施例4:トリボ帯電量(μA) 5.5 実施例5: 〃 6.0
<Embodiments 4 to 5> The g-t in Embodiment 2
Vinyl chloride in the same manner as in Example 2 except that the barium butylsalicylate salt was changed to magnesium di-t-butylsalicylate (Example 4) or strontium di-t-butylsalicylate (Example 5). A resin composition for powder coating of a base resin was produced. The evaluation results of the triboelectric charging characteristics of the above coating resin composition were as follows. Example 4: Tribo charge amount (μA) 5.5 Example 5: 〃 6.0

【0017】<比較例1>ジ−t−ブチルサリチル酸バ
リウム塩を使用しない点以外は、すべて実施例1と同様
にして塩化ビニル系樹脂の粉体塗装用樹脂組成物を製造
した。該塗装用樹脂組成物についての摩擦帯電特性の評
価結果は、トリボ帯電量で0.8μAであり、塗装のた
めに必要な最低帯電量の2μAに達していなかった。
Comparative Example 1 A vinyl chloride resin powder coating resin composition was produced in the same manner as in Example 1, except that barium di-t-butylsalicylate was not used. The evaluation result of triboelectric charging characteristics of the coating resin composition was 0.8 μA in triboelectric charge amount, which did not reach the minimum charge amount of 2 μA necessary for coating.

【0018】[0018]

【発明の効果】本発明によれば、熱可塑性樹脂の粉末を
主成分とし、かつ摩擦により帯電し易い粉体塗装用樹脂
組成物が容易に得られ、該組成物は、何らの問題もな
く、摩擦帯電方式の静電塗装に適用できる。
EFFECTS OF THE INVENTION According to the present invention, a resin composition for powder coating, which contains a thermoplastic resin powder as a main component and is easily charged by friction, can be easily obtained, and the composition has no problems. Applicable to triboelectric electrostatic coating.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 サリチル酸又はアルキルサルチル酸のア
ルカリ土金属塩を熱可塑性樹脂の粉末に混合してなる、
摩擦帯電方式の静電粉体塗装用樹脂組成物。
1. A mixture of an alkaline earth metal salt of salicylic acid or alkylsalicylic acid with a powder of a thermoplastic resin.
A resin composition for triboelectric electrostatic powder coating.
JP1784794A 1994-01-18 1994-01-18 Resin composition for electrostatic coating Pending JPH07207197A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1784794A JPH07207197A (en) 1994-01-18 1994-01-18 Resin composition for electrostatic coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1784794A JPH07207197A (en) 1994-01-18 1994-01-18 Resin composition for electrostatic coating

Publications (1)

Publication Number Publication Date
JPH07207197A true JPH07207197A (en) 1995-08-08

Family

ID=11955065

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1784794A Pending JPH07207197A (en) 1994-01-18 1994-01-18 Resin composition for electrostatic coating

Country Status (1)

Country Link
JP (1) JPH07207197A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5936046A (en) * 1996-12-31 1999-08-10 Shell Oil Company Epoxy resin with monoglycidyl-capped aryl amidopolyamine
US6160040A (en) * 1996-12-31 2000-12-12 Shell Oil Company Water borne capped ester containing epoxy amine adduct curing agents compositions for self-curing epoxy resins at ambient or sub-ambient temperatures
US6180727B1 (en) 1996-12-31 2001-01-30 Shell Oil Company Capped ester containing epoxy amine adduct curing agents for curing epoxy resins at ambient or sub-ambient temperatures without external catalysts

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5936046A (en) * 1996-12-31 1999-08-10 Shell Oil Company Epoxy resin with monoglycidyl-capped aryl amidopolyamine
US6160040A (en) * 1996-12-31 2000-12-12 Shell Oil Company Water borne capped ester containing epoxy amine adduct curing agents compositions for self-curing epoxy resins at ambient or sub-ambient temperatures
US6180727B1 (en) 1996-12-31 2001-01-30 Shell Oil Company Capped ester containing epoxy amine adduct curing agents for curing epoxy resins at ambient or sub-ambient temperatures without external catalysts

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