Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0472859B2 - - Google Patents
[go: Go Back, main page]

JPH0472859B2 - - Google Patents

Info

Publication number
JPH0472859B2
JPH0472859B2 JP58012007A JP1200783A JPH0472859B2 JP H0472859 B2 JPH0472859 B2 JP H0472859B2 JP 58012007 A JP58012007 A JP 58012007A JP 1200783 A JP1200783 A JP 1200783A JP H0472859 B2 JPH0472859 B2 JP H0472859B2
Authority
JP
Japan
Prior art keywords
thermosetting resin
microcapsules
resins
weight
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 - Lifetime
Application number
JP58012007A
Other languages
Japanese (ja)
Other versions
JPS59136348A (en
Inventor
Tadashi Bando
Nakatsugu Nakamura
Kazuo Akagane
Akira Shintani
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.)
SANTO KAKOGYO KK
Original Assignee
SANTO KAKOGYO KK
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 SANTO KAKOGYO KK filed Critical SANTO KAKOGYO KK
Priority to JP58012007A priority Critical patent/JPS59136348A/en
Publication of JPS59136348A publication Critical patent/JPS59136348A/en
Publication of JPH0472859B2 publication Critical patent/JPH0472859B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、保護ライニング材に適用し好適な耐
摩耗性に優れた熱硬化性樹脂組成物に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a thermosetting resin composition having excellent abrasion resistance and suitable for use as a protective lining material.

(従来の技術) ポリウレタン系樹脂、エポキシ系樹脂等の熱硬
化性樹脂は、その優れた物性から、従来、工場、
事務所等の床材、歩車道等の路面材料、砕石プラ
ント等の保護ライニング材等に使用されている
が、これ等の用途において再施工が必要となる要
因は、摩耗による損傷である場合が圧倒的に多
く、従つて耐摩耗性を向上せしめ、できる限り長
期間にわたつて性能を発揮し続けることが望まれ
ている。
(Prior art) Thermosetting resins such as polyurethane resins and epoxy resins have traditionally been used in factories due to their excellent physical properties.
It is used as flooring material for offices, etc., road surface material for pedestrian walkways, etc., and protective lining material for crushed stone plants, etc., but in these applications, the reason why re-installation is required is often damage due to wear. There is an overwhelming desire to improve wear resistance and continue to exhibit performance for as long as possible.

ところで、熱硬化性樹脂に耐摩耗性向上のため
シリコン油、弗素樹脂などを配合することは特公
昭40−13002号公報、特開昭51−107341号公報な
どに記載されて公知である。
By the way, it is known that silicone oil, fluororesin, etc. are blended into thermosetting resins in order to improve wear resistance, as described in Japanese Patent Publication No. 13002/1982 and Japanese Patent Application Laid-open No. 107341/1989.

しかし、これら公知のものは成形品を得る樹脂
材料に対するものであつて、その後の成形工程を
必須としており、保護ライニング材に適用されて
いる硬化剤を含有し常温硬化性のポリウレタン樹
脂又はエポキシ樹脂にそのまま適用するには適し
ていない。
However, these known methods are for the resin material from which the molded product is obtained, and require a subsequent molding process, and are made using polyurethane resin or epoxy resin containing a curing agent and curing at room temperature, which is applied to the protective lining material. Not suitable for direct application.

(発明が解決しようとする課題) 本発明者らは、上述の事情に対処し、ライニン
グ剤として従来の熱硬化性樹脂の耐摩耗性を向上
せしめるべく鋭意検討を行い、その結果、常温硬
化性のポリウレタン樹脂、エポキシ樹脂から選ば
れた熱硬化性樹脂にフツ素樹脂又はシリコーン樹
脂内包マイクロカプセルを所要量混入することに
より耐摩耗性を向上し得ることを知見し、本発明
を完成するに至つた。
(Problems to be Solved by the Invention) In order to address the above-mentioned circumstances, the present inventors conducted intensive studies to improve the abrasion resistance of conventional thermosetting resins as lining agents, and as a result, found that It was discovered that abrasion resistance could be improved by mixing a required amount of fluororesin or silicone resin-encapsulated microcapsules into a thermosetting resin selected from polyurethane resins and epoxy resins, and this led to the completion of the present invention. Ivy.

もとより、油分をマイクロカプセル内に封入
し、樹脂と混合させることは特公昭48−43374号
公報などに記載され公知であるが、従来のかかる
混合物は軸受などの成形に使用され、母材の中に
油粒子が独立した細胞状に存在する含油プラスチ
ツク成形品とするもので、本発明の如きライニン
グ材に適用するものではない。
Of course, it is well known that oil is encapsulated in microcapsules and mixed with resin, as described in Japanese Patent Publication No. 48-43374. Conventionally, such mixtures are used for molding bearings, etc. This is an oil-impregnated plastic molded article in which oil particles exist in the form of independent cells, and is not applicable to the lining material of the present invention.

即ち、本発明は特に前記熱硬化性樹脂と前記樹
脂内包マイクロカプセルの混合により保護ライニ
ング材としての熱硬化性樹脂組成物を提供し、従
来の保護ライニング層の耐摩耗性の大幅な向上を
図ることを目的とするものである。
That is, the present invention particularly provides a thermosetting resin composition as a protective lining material by mixing the thermosetting resin and the resin-encapsulated microcapsules, thereby significantly improving the abrasion resistance of the conventional protective lining layer. The purpose is to

(課題を解決するための手段) しかして上記目的に適合する本発明は(イ)常温硬
化性のポリウレタン系樹脂、エポキシ系樹脂から
なる群より選ばれた少なくとも1種の熱硬化性樹
脂および(ロ)フツ素樹脂、シリコーン樹脂からなる
群より選ばれる少なくとも1種を内包してなるマ
イクロカプセルを含有する組成物であつて、マイ
クロカプセルの含有量が1乃至60重量%である熱
硬化性樹脂組成物を提供するものである。
(Means for Solving the Problems) The present invention, which satisfies the above objects, consists of (a) at least one thermosetting resin selected from the group consisting of room temperature curable polyurethane resins and epoxy resins; b) A composition containing microcapsules containing at least one selected from the group consisting of fluororesins and silicone resins, the thermosetting resin having a microcapsule content of 1 to 60% by weight. A composition is provided.

上記本発明における熱硬化性樹脂としては公知
の熱硬化性樹脂が適宜使用可能であるが、施工の
迅速性および物性上より特に常温硬化性のポリウ
レタン系樹脂もしくはエポキシ系樹脂は最も好適
である。
As the thermosetting resin in the present invention, any known thermosetting resin can be used as appropriate, but room temperature curable polyurethane resins or epoxy resins are particularly preferred from the viewpoint of speed of construction and physical properties.

またマイクロカプセルに内包されるフツ素樹
脂,シリコーン樹脂としても公知のものが使用さ
れるが、これらは常温でグリース状であることが
好ましい。
Also, known fluororesins and silicone resins to be encapsulated in microcapsules are used, but these are preferably grease-like at room temperature.

なお、マイクロカプセル化は既知のいずれの方
法によつても容易に行うことができる。
Note that microencapsulation can be easily performed by any known method.

本発明の熱硬化性樹脂組成物は、上記した熱硬
化性樹脂およびマイクロカプセルを十分混合する
ことにより得られるが、組成物中のマイクロカプ
セルの含有量は1乃至60重量%であることが肝要
である。この場合、含有されるマイクロカプセル
の量が1重量%より少ない場合には十分な耐摩耗
性が得られず、また60重量%を越える場合には硬
化物の引つ張り、引き裂き強さ等の物性が低下す
るので好ましくない。
The thermosetting resin composition of the present invention can be obtained by sufficiently mixing the above-mentioned thermosetting resin and microcapsules, but it is important that the content of microcapsules in the composition is 1 to 60% by weight. It is. In this case, if the amount of microcapsules contained is less than 1% by weight, sufficient wear resistance cannot be obtained, and if it exceeds 60% by weight, the tensile strength, tear strength, etc. of the cured product may deteriorate. This is not preferred because the physical properties deteriorate.

なお、本発明の熱硬化性樹脂組成物には、必要
に応じて、酸化チタン等の顔料、クレー等のフイ
ラー、消泡剤、酸化防止剤、分散安定剤、ダレ止
め剤等の添加剤を添加することができる。
The thermosetting resin composition of the present invention may contain additives such as pigments such as titanium oxide, fillers such as clay, antifoaming agents, antioxidants, dispersion stabilizers, anti-sag agents, etc., as necessary. Can be added.

(作用) 本発明組成物によれば、これを前記保護ライニ
ング材等として使用したとき、熱硬化性樹脂硬化
物ライニング材の耐摩耗性は著しく改良され、加
えて作業性も改善される。
(Function) According to the composition of the present invention, when it is used as the protective lining material, etc., the abrasion resistance of the cured thermosetting resin lining material is significantly improved, and in addition, the workability is also improved.

(実施例) 以下、本発明を実施例により説明する。例中、
部は重量部を表わす。
(Example) Hereinafter, the present invention will be explained with reference to Examples. In the example,
Parts represent parts by weight.

実施例 1 スミカダインF310(硬化材含有ポリウレタン樹
脂系組成物、住友化学社品)100重量部に常温で
の動粘度が50cSt(センチストークス)のポリジメ
チルシロキサンを内包するマイクロカプセル(松
本油脂社品)20重量部を添加し、充分に攪拌棒で
混合し組成物を得、これを離型剤を予め塗布した
ガラス板上に流し込み、厚さ2mmのシート状に注
型した。7日間室温にて養生した後、荷重1Kg、
1000回転の条件下で、テーバー式耐摩耗性試験を
行つた。その結果、摩耗輪H22での重量損失は40
mgであつた。
Example 1 Microcapsules containing polydimethylsiloxane having a kinematic viscosity of 50 cSt (centistokes) at room temperature in 100 parts by weight of Sumikadyne F310 (curing agent-containing polyurethane resin composition, Sumitomo Chemical Co., Ltd.) (Matsumoto Yushi Co., Ltd.) 20 parts by weight were added and thoroughly mixed with a stirring rod to obtain a composition, which was poured onto a glass plate coated with a mold release agent in advance and cast into a sheet with a thickness of 2 mm. After curing at room temperature for 7 days, load 1Kg,
A Taber type wear resistance test was conducted under the condition of 1000 rotations. As a result, the weight loss on the worn wheel H22 is 40
It was mg.

比較例 1 マイクロカプセルを添加せずに実施例1と同様
に行つた実験では、重量損失は110mgであつた。
Comparative Example 1 In an experiment conducted as in Example 1 without the addition of microcapsules, the weight loss was 110 mg.

実施例 2 トーコー(Toko)エスエポ#500(硬化剤含有
エポキシ系樹脂組成物、東興アスフアルト社品)
100重量部に、常温で10000cStのポリジメチルシ
ロキサンを内包したマイクロカプセル(松本油脂
社品)40重量部を加え、攪拌棒で充分混合を行
い、組成物を得、これを予め、離型剤を塗布した
ガラス板上に流し込み、厚さ2mmのシート状に注
型した。3日間放置後、得られたシートを、実施
例1と同様にして摩耗試験を行つたところ、摩耗
による重量損失は30mgであつた。
Example 2 Toko S-Epo #500 (epoxy resin composition containing a curing agent, manufactured by Toko Asphalt Co., Ltd.)
To 100 parts by weight, 40 parts by weight of microcapsules containing polydimethylsiloxane (Matsumoto Yushi Co., Ltd.) containing 10,000 cSt at room temperature were added and thoroughly mixed with a stirring rod to obtain a composition. It was poured onto a coated glass plate and cast into a 2 mm thick sheet. After standing for 3 days, the resulting sheet was subjected to an abrasion test in the same manner as in Example 1, and the weight loss due to abrasion was 30 mg.

比較例 2 実施例2において、マイクロカプセルを添加せ
ずに摩耗試験を行つた結果、摩耗による重量損失
は130mgであつた。
Comparative Example 2 In Example 2, an abrasion test was conducted without adding microcapsules, and as a result, the weight loss due to abrasion was 130 mg.

(発明の硬化) 本発明熱硬化性樹脂組成物は以上のようにフツ
素樹脂、シリコーン樹脂からなる群より選ばれた
少なくとも1種を内包してなるマイクロカプセル
をポリウレタン系樹脂又はエポキシ系樹脂からな
る熱硬化性樹脂に所定量混合組成せしめたもので
あり、従来保護ライニング材に適用されている熱
硬化性樹脂に比し耐摩耗性が著しく向上し、摩耗
による損傷を大幅に低減して性能を長期にわたり
維持することができると共に、マイクロカプセル
に内包して混合するため、熱硬化性樹脂との混合
も容易で、かつ保護ライニング作業に際しても作
業性を著しく良好ならしめることができる。
(Curing of the Invention) As described above, the thermosetting resin composition of the present invention includes microcapsules containing at least one selected from the group consisting of fluorocarbon resins and silicone resins, which are made of polyurethane resin or epoxy resin. It is made by mixing a predetermined amount of a thermosetting resin, and has significantly improved abrasion resistance compared to the thermosetting resin conventionally used for protective lining materials, greatly reducing damage caused by abrasion and improving performance. can be maintained for a long period of time, and since it is encapsulated in microcapsules and mixed, it is easy to mix with the thermosetting resin, and workability can be significantly improved during protective lining work.

Claims (1)

【特許請求の範囲】[Claims] 1 (イ)常温硬化性のポリウレタン系樹脂、エポキ
シ系樹脂からなる群より選ばれた少なくとも1種
の熱硬化性樹脂及び(ロ)フツ素樹脂、シリコーン樹
脂からなる群より選ばれる少なくとも1種を内包
してなるマイクロカプセルを含有する組成物であ
つて、マイクロカプセルの含有量が1乃至60重量
%であることを特徴とするライニング材用熱硬化
性樹脂組成物。
1. (a) at least one thermosetting resin selected from the group consisting of room temperature curable polyurethane resins and epoxy resins; and (b) at least one thermosetting resin selected from the group consisting of fluororesins and silicone resins. 1. A thermosetting resin composition for a lining material, the composition containing microcapsules, wherein the content of the microcapsules is 1 to 60% by weight.
JP58012007A 1983-01-26 1983-01-26 Thermosetting resin composition Granted JPS59136348A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58012007A JPS59136348A (en) 1983-01-26 1983-01-26 Thermosetting resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58012007A JPS59136348A (en) 1983-01-26 1983-01-26 Thermosetting resin composition

Publications (2)

Publication Number Publication Date
JPS59136348A JPS59136348A (en) 1984-08-04
JPH0472859B2 true JPH0472859B2 (en) 1992-11-19

Family

ID=11793526

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58012007A Granted JPS59136348A (en) 1983-01-26 1983-01-26 Thermosetting resin composition

Country Status (1)

Country Link
JP (1) JPS59136348A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE50013562D1 (en) * 2000-06-20 2006-11-16 Abb Research Ltd Potting compounds for the production of electrical insulation
JP5141857B2 (en) * 2006-09-08 2013-02-13 信越化学工業株式会社 Epoxy resin composition and semiconductor device
WO2009055772A1 (en) * 2007-10-26 2009-04-30 The Board Of Trustees Of The University Of Illinois Solvent-promoted self-healing materials

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4843374A (en) * 1971-10-02 1973-06-22
JPS51107341A (en) * 1975-03-18 1976-09-22 Sumitomo Electric Industries GANYUPURA SUCHITSUKUSOSEIBUTSU

Also Published As

Publication number Publication date
JPS59136348A (en) 1984-08-04

Similar Documents

Publication Publication Date Title
Alkadasi et al. Effect of coupling agent on the mechanical properties of fly ash–filled polybutadiene rubber
EP1101484A3 (en) Dental fillers
JP2739233B2 (en) Silicone granules containing mineral oil
DE2621796C2 (en)
EP0586153A2 (en) Silicone Compositions
JPH04348143A (en) Silicone rubber powdery article and production thereof
DE59910301D1 (en) USE OF THERMOPLASTIC POLYESTER MOLDINGS FOR VEHICLE INTERIOR APPLICATIONS
DE69600637T2 (en) Organosiloxane compositions that provide machinable and erosion-resistant elastomers
DE2911583A1 (en) BRAKE BLOCK MATERIAL
CN109666224A (en) Sealing strip made of a kind of TPV of lasting self-lubricating and preparation method thereof the and TPV
CN1015109B (en) glass fiber reinforced polyvinyl chloride blends with improved heat distortion and tensile strength
Savotchenko et al. The improvement of mechanical properties of repair and construction compositions based on epoxy resin with mineral fillers
JPH0472859B2 (en)
EP0522738A1 (en) Organosiloxane compositions and use thereof
JP4961542B2 (en) Organic polymer composition, method for producing the same, and method for producing wet masterbatch
Tomar et al. Mechanical properties of mica‐filled PBT/ABAS composites
Pongdong et al. Thermodynamically and kinetically favored locations of rice husk ash particles in the phase structure, and the properties of epoxidized natural rubber/thermoplastic polyurethane blends
CN117964279B (en) A heavy-load asphalt pavement modifier, its preparation method and application
US6824832B2 (en) Thermosetting plastic composition
DE20206801U1 (en) Additive made from rubber granulate and biopolymer binder, preferably suitable for bitumen production
KR100580595B1 (en) Performanced-improving method of PET recycling polymer concrete to apply highly efficient nano particles
JP2752896B2 (en) Synthetic resin coated flooring
JPH0269509A (en) Molding material of phenolic resin
Lirio et al. Effects of Hardener Content on Properties of Epoxy-Granite Composite Artificial Stones
Quddos et al. Effect of the fillers contents on the chemical, mechanical and thermal properties of polymer composites