JPS61268445A - Flexible vinyl chloride group resin tape for sheathing - Google Patents

Flexible vinyl chloride group resin tape for sheathing

Info

Publication number
JPS61268445A
JPS61268445A JP60109412A JP10941285A JPS61268445A JP S61268445 A JPS61268445 A JP S61268445A JP 60109412 A JP60109412 A JP 60109412A JP 10941285 A JP10941285 A JP 10941285A JP S61268445 A JPS61268445 A JP S61268445A
Authority
JP
Japan
Prior art keywords
weight
parts
sheet
microns
vinyl chloride
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.)
Granted
Application number
JP60109412A
Other languages
Japanese (ja)
Other versions
JPH0263062B2 (en
Inventor
藤木 時男
三原 信一
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.)
Tosoh Corp
Original Assignee
Toyo Soda Manufacturing 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 Toyo Soda Manufacturing Co Ltd filed Critical Toyo Soda Manufacturing Co Ltd
Priority to JP60109412A priority Critical patent/JPS61268445A/en
Publication of JPS61268445A publication Critical patent/JPS61268445A/en
Publication of JPH0263062B2 publication Critical patent/JPH0263062B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A30/00Adapting or protecting infrastructure or their operation
    • Y02A30/14Extreme weather resilient electric power supply systems, e.g. strengthening power lines or underground power cables

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、T業用水、上水、渇水、冷水、蒸気、各種冷
媒あるいは、工業薬品などの輸送配管4tらびに塔槽類
の保温、保冷Hの保護装飾外装、および電線など線材の
絶縁被覆に用いられる軟質ポリ塩化ビニル系テープに関
するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is applicable to the heat insulation of 4 tons of transportation pipes and towers and tanks for industrial water, clean water, drought water, cold water, steam, various refrigerants, industrial chemicals, etc. This invention relates to a soft polyvinyl chloride tape used as a protective decorative exterior for cold storage H and as an insulating coating for wires such as electric wires.

本発明の軟質ポリ塩化ビニル系テープは、配管や塔槽類
の装飾および保護外装に用いられる他、すでに施工され
ている金属板外装材が腐蝕あるいは破損し、その機能が
失なわれた部分の補作用としても有用である。本発明の
テープは、特に屋外使用に有効である。
The soft polyvinyl chloride tape of the present invention can be used for decoration and protective sheathing of piping and towers and tanks, as well as for areas where the existing metal plate sheathing material has corroded or been damaged and has lost its function. It is also useful as a complementary action. The tape of the present invention is particularly effective for outdoor use.

[従来の技術] 従来、配管ある・いは塔槽類の保温、保冷材の外装には
、厚さが300〜500ミクロンの亜鉛鉄板、あるいは
カラー鋼板などの金属板が広く用いられている。これら
金属板による外装施Tにおいては、板金加工の特殊技能
が必要であるが、現今、板金加工技能者の不足が、配管
あるいはブラント業界で問題になりつつある。
[Prior Art] Conventionally, metal plates such as galvanized iron plates or colored steel plates with a thickness of 300 to 500 microns have been widely used for the exterior of heat insulating and cold insulating materials for piping, towers and tanks. Special skill in sheet metal processing is required for the exterior application T using these metal plates, but the shortage of sheet metal processing technicians is currently becoming a problem in the piping and blunting industries.

また、金属板外装において、金属板同志の継目接続は、
一般に、ハI!掛IJT法が広く採用されているが、こ
のT法では1.1字型に板金加−「した金属板端部を′
I−1いにかみ合せた構)告どなる。従って、1字型の
溝の深さ、あるいは、かみ合口が充分でないと配管ある
いは塔槽の振動、Parsあるいは収縮によって板の接
続が外れるという事故がしばしば発生り−る。この様な
場合、ハゼ掛けが外れた箇所から雨水が侵入して断熱材
を濡らすので断熱効果が低下り゛るという問題が発生覆
る。さらに、海岸近くの工場、あるいは、M性又はアル
カリ性雰囲気にある工場では、金属の腐蝕が早く、外装
の補修照度が高い。これら金属板外装材は、表面塗装な
どにJ:って耐蝕処理がなされているものの塗装表面に
一1ズが発生したとき、あるいは、塗膜の劣化などによ
る塗膜の脱落によって金属面が直接大気に触れるように
なるときは、短時間に金属の腐蝕が進行する。
In addition, in the metal plate exterior, the seam connection between metal plates is
In general, HaI! The hanging IJT method is widely adopted, but in this T method, the edge of the metal plate that has been added to the shape of 1.
I-1 (I-1) was yelled at. Therefore, if the depth of the single-shaped groove or the engagement opening is insufficient, accidents often occur in which the plates become disconnected due to vibration, pars, or contraction of the piping or tower. In such a case, rainwater enters from the place where the hook has come off and wets the insulation material, causing a problem that the insulation effect is reduced. Furthermore, in factories near the coast or in factories in M or alkaline atmospheres, metals corrode quickly and the exterior repair lighting intensity is high. Although the surface coating of these metal plate exterior materials has been subjected to corrosion-resistant treatment, when scratches occur on the painted surface, or when the paint film falls off due to deterioration of the paint film, the metal surface may be directly exposed. When metal comes into contact with the atmosphere, corrosion progresses in a short period of time.

また、配管あるいは塔槽の外装施工方法は高所での作業
が多く、特殊技能や■貝類を用いることイ【く容易に施
工できることが強く望まれている。このような観点から
、7711性と耐蝕性とに優れている防蝕用ヒニルテー
プ、電気絶縁用テープあるいは布製テープl【どが、鋼
板製外装材と同様の目的で利用されている。しかし、こ
れら高分子材料からなる外装材は、環境のおだやかな屋
内配管などの外装材としては十分利用し得るが、太陽光
の直射、雨風、気温の高低など環境条件が厳しい屋外で
使用すると、短期間、例えば1年から2年程度で材料が
劣化し、はがれ、亀裂が生じ遂には自然切断に芋って外
装材としての機能が夫なはれてしまう。
In addition, many of the methods for constructing the exterior of piping or towers and tanks involve work at high places, and it is strongly desired that the construction can be done easily by using special skills or shellfish. From this point of view, corrosion-resistant vinyl tape, electrical insulation tape, and cloth tape, which have excellent 7711 properties and corrosion resistance, are used for the same purpose as steel plate exterior materials. However, although exterior materials made of these polymer materials can be fully used as exterior materials for indoor piping in a mild environment, when used outdoors where environmental conditions are harsh such as direct sunlight, rain and wind, and high and low temperatures, Over a short period of time, for example, one to two years, the material deteriorates, peels, cracks, etc., and eventually breaks down naturally and loses its function as an exterior material.

[発明が解決しようとする問題点] このように従来の配管あるいは塔槽類の外装施工方法な
らびに材料には多くの解決づべき問題点がある。本発明
の目的は施二「性に優れ、特に長期間の屋外使用に耐え
得るテープ状外装材をflJtすることにある。従って
、本発明の解決課題は、従来の防蝕用ビニルテープ、電
気絶縁テープあるいは布製テープなどを屋外使用したと
ぎに生ずる問題 5一 点、すなはち、紫外線あるいは夏期高温時におけるテー
プ材質の劣化を防+1し、かつ長期に7gって装飾性と
外装材としての機能を保持し得るためのテープ構造及び
月質段81にある。
[Problems to be Solved by the Invention] As described above, there are many problems that need to be solved with the conventional methods and materials for exterior construction of piping or towers and tanks. The purpose of the present invention is to provide a tape-like exterior material that has excellent durability and can withstand long-term outdoor use. Problems that arise when tapes or cloth tapes are used outdoors: 5. One point is to prevent the tape material from deteriorating due to ultraviolet rays or high temperatures in the summer, and to maintain its decorative properties and function as an exterior material with a long-term maintenance of 7g. There is a tape structure and a lunar stage 81 for holding.

本発明者らは、従来から防蝕用外装テープとして広く屋
外用途にも用いられている軟質ポリ塩化ビニルテープを
屋外で使用するとき、何故類1]時に劣化し機能の欠損
が起るのかを詳細に検問した結果、次のことが判った。
The present inventors have investigated in detail why soft polyvinyl chloride tape, which has traditionally been widely used as a corrosion-resistant exterior tape for outdoor applications, deteriorates and loses functionality when used outdoors. As a result of the investigation, the following was found.

すなわら、 1)用いられている可塑剤が揮発しく特に夏季に起る)
、可塑剤含量の約60%以上の可塑剤が揮発によって失
なわれるど、材料内部に微細な空孔が生じ、それによっ
てI質的な欠陥と応力集中によって容易に材料の脆性(
もろくなる現象)破損が起る。
1) The plasticizer used is volatile, especially in the summer)
, about 60% or more of the plasticizer content is lost through volatilization, and fine pores are created inside the material, which easily causes material defects and stress concentration, which can lead to brittleness of the material (
(Phenomenon of becoming brittle) Breakage occurs.

2)紫外線にJ:つて材料の分子嶺低下が起り、伸び、
及び強度の低下を誘引する。特に、伸びの低下は材料の
弾性低下を意味し陥性破壊の原因と4する。
2) When exposed to ultraviolet rays, the molecular peaks of the material decrease, elongate,
and induce a decrease in strength. In particular, a decrease in elongation means a decrease in the elasticity of the material, which is considered to be a cause of pitting failure.

以上、軟質塩化ビニルテープを屋外使用で使用したとき
に起る劣化原因を二つの要因に分けて述べたが、実際に
はこの二つの要因が相乗的に起るので、軟質塩化ビニル
テープの屋外使用での劣化原因は非常に複雑のように見
える。したがって、長期間にnり屋外で外装用どして軟
質塩化ビニルテープをその機能を失なわせずに使用する
ためには、軟質ポリ塩化ビニルテープの劣化原因どなる
上述の二つの要因を少なくとも同時に解決する必要があ
る。
Above, we have divided the causes of deterioration that occur when soft vinyl chloride tape is used outdoors into two factors, but in reality, these two factors occur synergistically, so it is important to note that when soft vinyl chloride tape is used outdoors, The causes of deterioration during use appear to be very complex. Therefore, in order to use soft PVC tape for long-term outdoor purposes without losing its functionality, it is necessary to check at least the above two factors that cause the deterioration of soft PVC tape at the same time. Needs to be resolved.

これの考えられる解決方法は、可塑剤の揮発性を抑制す
るため高分子間の可塑剤を用い、かつ耐候性を付与する
目的で力〜ボンブラックあるいは、酸化チタンを混入す
ることであるが、これでは屋外配管外装用として要求さ
れる装飾↑1(例えば、シルバー色に着色する)が失な
われてしまう。装飾性を保持する考えられる一つの方法
どしては、高分子間の可塑剤と肴色判を含む装飾用シル
トどカーボンブラックを含む耐候性をもたせたシートを
前者を外装どして重ねて巻きつ・ノる方法があるが、単
に重ね巻きしただけでは長期の使用により装飾層部分に
劣化が生じ、脆性に基因すると思われる弾着の低下と一
部表面亀裂の発生によって装飾層がゆるみ、下に巻いた
耐候層テープが露出してしまい前記問題を解決Jること
は出来ない。また、重ね巻きの方法は  B1カーボン
ブラック入り耐Hアープを巻いた上に装飾テープをさら
に巻かなIJれLt <Lらず、施工が二億手間になり
繁雑になるという欠点を有する。本発明者らは、この様
な問題が生じない、施工性が白い配管外装材を得るため
の実験的研究を重ねた結束、屋外使用に要求される長期
に万る耐熱性と耐候性とを保持するためには以下の手段
によりこれらの点を解決し得ることを見い出し本発明に
到達した。
A possible solution to this problem is to use an interpolymer plasticizer to suppress the volatility of the plasticizer, and to add carbon black or titanium oxide to impart weather resistance. In this case, the decoration ↑1 (for example, silver coloring) required for the exterior of outdoor piping is lost. One possible way to maintain the decorative properties is to layer the former with a weather-resistant sheet containing decorative silt or carbon black, which contains a plasticizer between polymers and a tint. There is a winding and winding method, but if you simply wrap it in layers, the decorative layer will deteriorate due to long-term use, and the decorative layer will become loose due to a decrease in the adhesion, which is thought to be due to brittleness, and the occurrence of surface cracks in some areas. However, the weather-resistant layer tape wrapped underneath is exposed and the above problem cannot be solved. In addition, the overlapping method has the disadvantage that the decorative tape must be further wrapped on top of the B1 carbon black-containing H-arp resistant material, which requires 200,000,000 hours of work and is complicated. The present inventors have developed a binding material that has undergone extensive experimental research to obtain a pipe exterior material that does not cause such problems and is easy to work with, and has the long-term heat resistance and weather resistance required for outdoor use. In order to maintain this, it was discovered that these points could be solved by the following means, and the present invention was achieved.

E問題を解決するだめの手段] 即ち、ぞの解決手段は、重合度が650以上のポリ塩化
ビニル系樹脂100市量部に、一種または二種以上の下
記から選ばれる低揮発性耐熱可塑剤を少<’K <ども
40市昂%以上含む可塑剤20〜80重量部、イf愈の
着色剤およびポリ塩化ビニル系樹脂に通常使用される安
定剤を添加した、厚さが50ミクロンから1000ミク
ロンの外部可塑化軟質塩化ビニル系樹脂シーi−(1)
と、重合度が650以上のポリ塩化ビニル系樹脂100
市量部に、特に種類を選ばない可塑剤O〜80重吊部重
量常使用される安定剤および少なくとも0.5重量%以
上のカーボンブラック及び/又は酸化チタンを添加した
、厚さが50ミクロンから1600ミクロンの内部又は
外部可塑化軟質塩化ビニル系樹脂シー1〜(If)を熱
FIJ、着によって一体に接合することにあり、したが
って本発明は、かくして得られる厚さが100ミクロン
から1700ミクロンの外装用軟質塩化ビニル系樹脂テ
ープにある。
A solution to problem E] That is, the solution is to add one or more low-volatility heat-resistant plasticizers selected from the following to 100 parts of a polyvinyl chloride resin with a degree of polymerization of 650 or more. 20 to 80 parts by weight of plasticizer containing 40% or more, if desired colorant and stabilizers commonly used in polyvinyl chloride resins, with a thickness from 50 microns. 1000 micron externally plasticized soft vinyl chloride resin Sea I-(1)
and polyvinyl chloride resin 100 with a degree of polymerization of 650 or more.
A commercially available plasticizer of any type O~80, a commonly used stabilizer, and at least 0.5% by weight of carbon black and/or titanium oxide, with a thickness of 50 microns. The present invention consists in bonding together internally or externally plasticized soft vinyl chloride resin sheets 1-(If) from 100 microns to 1,600 microns by thermal FIJ, and the thickness thus obtained is from 100 microns to 1,700 microns. This is a soft vinyl chloride resin tape for exterior use.

シート(I)に用いる塩化ビニル系樹脂は、通常の塩化
ビニル重合体、塩化ビニル共重合体、例えば、酢酸ビニ
ルなどのカルボン酸エステルとの共重合体、エチレンな
どのオレフィン類どの共重合体であるが、特に塩化ビニ
ルの重合度が650以上LJIS  K6721による
)の重合体が、成型体とした際の引り柔軟性等の面で好
ましく、重合度が650に満たないものは強瘍低下の点
で好ましくない。
The vinyl chloride resin used for the sheet (I) may be a normal vinyl chloride polymer, a vinyl chloride copolymer, a copolymer with a carboxylic acid ester such as vinyl acetate, or an olefin copolymer such as ethylene. However, polymers with a vinyl chloride polymerization degree of 650 or higher (according to LJIS K6721) are particularly preferred in terms of tensile flexibility when formed into a molded product, and polymers with a polymerization degree of less than 650 are less effective in reducing ulcers. Unfavorable in some respects.

又シー1〜(1)を構成する塩化ビニル系樹脂に加える
低揮発性耐熱可塑剤は、次の群から選ばれる一種以上の
可塑剤を少むくとも40重量%以上含む可塑剤である。
The low-volatility heat-resistant plasticizer added to the vinyl chloride resin constituting Seas 1 to (1) is a plasticizer containing at least 40% by weight of one or more plasticizers selected from the following group.

1)グリコール類とジカルボン酸類、グリコール類、ジ
カルボン酸類及び脂肪酸類の重縮合反応で得られる粘度
が2500r)/25℃以−トの飽和ポリエステル系可
塑剤、 ii)粘度が80cp/25℃以上のトリメリット酸エ
ステル、エポキシ化太り油、エポキシ化あまに油、 iii )粘度が100Cr)/25℃以上のエポキシ
化脂肪1rステル系可塑剤、 iv)分子量が4001ス上のフタル酸系、デトラヒド
ロフタル耐系、アジピン酸系、アゼライン酸系。
1) A saturated polyester plasticizer with a viscosity of 2500 cp/25°C or higher obtained by the polycondensation reaction of glycols and dicarboxylic acids, glycols, dicarboxylic acids, and fatty acids; ii) A saturated polyester plasticizer with a viscosity of 80 cp/25°C or higher. trimellitic acid ester, epoxidized fattening oil, epoxidized linseed oil, iii) epoxidized fat with a viscosity of 100Cr)/25°C or higher, 1r ster plasticizer, iv) phthalic acid type with a molecular weight of 4001s or higher, Detra Hydrophthal-resistant, adipic acid, and azelaic acid.

セバシン酸系、クエン酸系、リン酸系可塑剤、V)テト
ラ−2−■デルヘキシルピロメリテート、テトラ−n−
オクヂルビ0メリテートのピロメリット酸エステル系可
塑剤、 −1〇 − vi)ジペンタエリスリトール、ペンタエリスリトール
エステル系可塑剤。
Sebacic acid type, citric acid type, phosphoric acid type plasticizer, V) Tetra-2-delhexylpyromellitate, Tetra-n-
Pyromellitic acid ester plasticizer of Okujirubi 0 mellitate, -10-vi) Dipentaerythritol, pentaerythritol ester plasticizer.

該耐熱可塑剤が40重量%未満の詩は、前述のように可
塑剤の揮発による材質的な欠陥が生じ材料の脆性破壊を
誘起するので好ましくない。可塑剤は塩化ビニル系樹脂
100重り部に対し20〜80重量部添加するが、可塑
剤量が20重量部に満たないときは材料の軟化効果が失
なわれ、また、80重量部を越えるとぎは材料の強度や
施工性に劣るので好ましくない。特に好ましい可塑剤の
使用範囲は30〜70重量部である。シート(1)に装
飾性を付与する着色剤としては、例えば、シルバーグレ
イに着色するためにはアルミニウム粉末が用いられる。
A material containing less than 40% by weight of the heat-resistant plasticizer is not preferable because, as mentioned above, material defects occur due to volatilization of the plasticizer and induce brittle fracture of the material. The plasticizer is added in an amount of 20 to 80 parts by weight per 100 parts by weight of the vinyl chloride resin. However, if the amount of plasticizer is less than 20 parts by weight, the softening effect of the material will be lost, and if it exceeds 80 parts by weight, is not preferable because it is inferior in material strength and workability. A particularly preferred range of plasticizer usage is 30 to 70 parts by weight. As a coloring agent that imparts decorative properties to the sheet (1), for example, aluminum powder is used to color the sheet (1) silver gray.

シート(TI)に用いる塩化ビニル系樹脂は特に種類を
選ばない。前記したシート(1)に用いる樹脂の他、内
部可塑化燻化ビニル系樹脂も用いることが出来る。内部
可塑化軟質塩化ビニル系樹脂としては■チレンービニル
エスデル共重合体又は、ポリウレタンに塩化ビニルをグ
ラフト申合した重合体を挙げることが出来る。
The type of vinyl chloride resin used for the sheet (TI) is not particularly limited. In addition to the resin used for the sheet (1) described above, an internally plasticized smoked vinyl resin can also be used. Examples of the internally plasticized soft vinyl chloride resin include (2) tyrene-vinyl esdel copolymer or a polymer obtained by grafting vinyl chloride onto polyurethane.

あるいはエチレン−ビニル■ステル共小合体と塩化ビニ
ル系樹脂又I;1、ポリウレタンと塩化ビニル系樹脂の
ごときブレンド体もまた用いることが出来る。まIこ、
シー1〜(11)に用いられる塩化ビニル系樹脂の可塑
化に用いる可塑剤は特に種類を選ばない。勿論前記」ノ
だ低揮発性耐熱可塑剤も用いられる。イの使用量はシー
ト(I)の場合と動揺であるが1、塩化ビニル系樹脂が
内部可塑化重合体である場合は可塑剤の使用量を零にす
るか相当量減量することが出来る。シート(IT)に耐
候性を付与するカーボンブラック及び/又は酸化チタン
は0.5重量%〜10重量%、好ましくは1重量%〜7
重串%の範囲で用いられる。0.5重量%に満たないと
きは耐候性を付与する効果が失なわれる。また、10重
量%を越える添加は耐候性の向上に連からない。安定剤
は通常塩化ビニル系樹脂に使用されるものが通常の使用
範囲において適正m選択使用される。尚、シート(I)
、シート(TI)には、例えば、ベンシフエノン系、ペ
ンシトリアゾール系、サリンレート系、シコウ酸アニリ
ド系、ヒンダードアミン系、フォルムアミジン系紫外線
吸収剤あるいは光安定剤、酸化防止剤を加えてシート(
1)の耐候性、耐熱性あるいはシート(TI)の安定性
を改善すること、ならびに炭酸力ルシュウムのごとき無
機フィラーを加えて表面粘着性を改良すること、ならび
に三酸化アンチモンおよび/またはほう酸亜鉛などの難
燃剤あるいは難燃助剤を加えて難燃性能を付与すること
、ならびに感圧接着剤をシート(TI)裏面に塗布して
感圧接着性を付与することも出来る。シート(I)の厚
さは50〜1000ミクロンとし、シート(TI)の厚
さは50〜1600ミク[lンとする。本発明は、この
様にして得たシート(I)とシート(IF)を熱融着さ
せて厚さ100〜1700ミクロンの一体シートとして
得るが、シート厚さが100〜1700ミクロンの範囲
外のものは施工性を悪くするので好ましくない。
Alternatively, a blend of an ethylene-vinyl ester copolymer and a vinyl chloride resin or a blend of polyurethane and a vinyl chloride resin can also be used. Maiko,
The type of plasticizer used for plasticizing the vinyl chloride resin used in Seams 1 to (11) is not particularly limited. Of course, the above-mentioned low-volatility heat-resistant plasticizers may also be used. The amount of plasticizer used is different from that of sheet (I), but if the vinyl chloride resin is an internally plasticized polymer, the amount of plasticizer used can be reduced to zero or considerably reduced. The amount of carbon black and/or titanium oxide that imparts weather resistance to the sheet (IT) is 0.5% to 10% by weight, preferably 1% to 7% by weight.
It is used within the range of %. When the amount is less than 0.5% by weight, the effect of imparting weather resistance is lost. Furthermore, addition of more than 10% by weight does not lead to improvement in weather resistance. As the stabilizer, those normally used for vinyl chloride resins are selected and used within the range of normal use. Furthermore, sheet (I)
To the sheet (TI), for example, a bencyphenone-based, pencitriazole-based, sarinlate-based, sikoic acid anilide-based, hindered amine-based, formamidine-based ultraviolet absorber, light stabilizer, or antioxidant is added to the sheet (TI).
1) Improving the weather resistance, heat resistance or stability of the sheet (TI), and improving the surface tackiness by adding an inorganic filler such as rhusium carbonate, and antimony trioxide and/or zinc borate, etc. It is also possible to impart flame retardant properties by adding a flame retardant or a flame retardant aid, or to impart pressure sensitive adhesive properties by applying a pressure sensitive adhesive to the back surface of the sheet (TI). The thickness of the sheet (I) is 50 to 1000 microns, and the thickness of the sheet (TI) is 50 to 1600 microns. In the present invention, sheet (I) and sheet (IF) thus obtained are thermally fused to form an integral sheet having a thickness of 100 to 1,700 microns. This is not desirable because it impairs the workability.

一体化したシート(I)シート(TI)は、被覆対象物
及び作業に適切な幅に切断してテープ状とし、これを装
飾層(シーI〜(I))が外側になるように配管あるい
は塔槽あるいは線材に例λば、ラセン状に巻つけて使用
する。
The integrated sheet (I) and sheet (TI) are cut into a tape shape to a width appropriate for the object to be coated and the work, and then piped or piped so that the decorative layers (sea I to (I)) are on the outside. For example, it is used by winding it in a spiral shape around a column or wire.

[発明の効果1 以十−説明したことにより、装飾性と耐熱性および耐候
性の三つの特性を兼ねそなえ、又極めて作業性の良好な
テープが得られる。
[Effects of the Invention 1-10] As explained above, a tape can be obtained which has the three characteristics of decorativeness, heat resistance and weather resistance, and also has extremely good workability.

[実施例1 以下実施例で本発明を更に説明覆る。[Example 1 The present invention will be further explained in the following examples.

(参考例) 25℃にお1ノる粘麻が6500センチポアズのポリエ
ステル系高分子量可塑剤を塩化ビニル樹脂100弗量部
に対し65重量部用い、着色料どしてアルミニウム粉末
を用い厚さ200ミクロンの装飾用軟質塩化ビニルシー
トを作成した。これとは別にカーボンブラック3重量%
と可塑剤(OOP)40重量部と前記ポリエステル系可
塑剤25重量部とを加え、耐候性を持たせた厚さ300
ミクロンの軟質塩化ビニルシートを作成、このカーボン
ブラック入りのシートを直径8 ctrtの円筒状にラ
セン状に巻き、さらに、その上に前記シルバー色に着色
した軟質塩化ビニルテープを車ねてう1?ン状に巻きつ
けた。(以後重ね巻きと呼ぶ)一方、前記厚さ200ミ
クロンの装飾用軟質塩化ビニルシーI〜と前記厚さ30
0ミクロンのカーボンブラックを3%混入した軟質塩化
ビニルシー1−とを熱融着によって一体に緊密に接合し
て成る厚さ500ミクロンの複層軟質塩化ビニルシー]
〜を装飾シルバ一層が−VになるJ:うに直径8 ct
trの円筒上に巻つけた。(以後複層−重巻きと叶ぶ)
この両者をサツシ11インウ■ザオメーターでブラック
パネル温醍63℃のもとて2000時間照射したところ
前記重ね巻きの装飾部分に劣化が生じ蝋付に基因すると
思われる弾性の低下と一部表面亀裂の発生によって装飾
層がゆるみ、下に巻いてあった黒色耐候性テープが露出
してしまった。この場合カーボンブラックを混入した軟
質塩化ビニル層はゆるみ、亀裂はなく、弾性力も保持さ
れていた。
(Reference example) Using 65 parts by weight of a polyester-based high molecular weight plasticizer with a viscosity of 6,500 centipoise at 25°C per 100 parts of vinyl chloride resin, and using aluminum powder as a coloring agent, a thickness of 200 centipoise was used. A micron decorative soft vinyl chloride sheet was created. In addition to this, carbon black 3% by weight
By adding 40 parts by weight of plasticizer (OOP) and 25 parts by weight of the polyester plasticizer, a thickness of 300 mm with weather resistance was added.
A micron soft vinyl chloride sheet is made, this carbon black-containing sheet is spirally wound into a cylindrical shape with a diameter of 8 ctrt, and the silver-colored soft vinyl chloride tape is placed on top of it. I wrapped it in a shape. (Hereinafter referred to as overlapping wrapping) On the other hand, the decorative soft vinyl chloride sheet I~ with a thickness of 200 microns and the above-mentioned 30 micron thick
A multi-layer soft vinyl chloride sheet with a thickness of 500 microns made by tightly bonding together a soft vinyl chloride sheet 1- containing 3% carbon black of 0 microns by heat fusion]
Decorate ~ with one layer of silver J: sea urchin diameter 8 ct
It was wrapped around the cylinder of tr. (Hereafter, it will come true as multi-layered - multi-layered)
When both of these were irradiated for 2,000 hours with a black panel temperature of 63°C using a satsushi 11-inch meter, the decorative parts of the overlapping wraps deteriorated, and the elasticity decreased and some surface cracks appeared due to the brazing. The outbreak loosened the decorative layer, exposing the black weather-resistant tape wrapped underneath. In this case, the soft vinyl chloride layer mixed with carbon black was loosened, had no cracks, and maintained its elasticity.

一方、同一試験条件のもとで複層−重巻きをテス1へし
たところ紫外線照射面の装飾層に一部変色と微細なひび
割れが見出されたが下層のカーボンブラック入り耐候性
テープからのは(す、脱落は仝くみられず、円筒への密
着性もなったく問題ないことが分った。また、JIII
性も一度の巻きつt)ですむのでl’lrr 壱に比べ
て施工性は倍加する。
On the other hand, when a multi-layered double-wrap was subjected to Test 1 under the same test conditions, some discoloration and fine cracks were found in the decorative layer on the UV irradiated surface, but there was some discoloration and fine cracks from the weather-resistant tape containing carbon black in the lower layer. (Yes, I didn't see any falling off, and there was no problem with the adhesion to the cylinder. Also, JIII
Since only one winding is required, the workability is doubled compared to l'lrr1.

以上の実験は重ね巻き及び複層−重巻きの両者について
紫IA線劣化の影響を中心に調べたものであるが、次に
耐熱性について調べた。ポリエステル系可塑剤に代え’
7.’ 2− エチルへキシルフタレート(r) OP
 )を樹脂100@吊部に対して50市01部を加え、
これに若干量の着色料としてアルミニウム粉末を加えて
厚さ200ミクロンの軟質塩化ビニルシー1〜を作成し
た。これどポリエステル系可塑剤を等Ml加えた厚さ2
00ミクロンの軟質テープを作成し温度121℃のもと
て240時間放胃下後可塑剤含量を測定したところDO
Pを用いたシートの可塑剤含mlは約40%低下するに
対し、高分子量ポリエステル系可塑剤を加えたものはた
かだか2.3重程度の減量しかみられなかった。
In the above experiments, the influence of violet IA ray deterioration was mainly investigated for both overlapping winding and multi-layer overlapping winding, and next, heat resistance was investigated. Instead of polyester plasticizer
7. ' 2-Ethylhexyl phthalate (r) OP
) to 100 parts of resin @ hanging part, add 50 parts and 01 parts,
A small amount of aluminum powder was added as a coloring agent to prepare soft vinyl chloride sheets 1 to 200 microns thick. Thickness 2 with equal ml of polyester plasticizer added
A soft tape with a diameter of 0.00 microns was prepared and the plasticizer content was measured after 240 hours of gastric feeding at a temperature of 121°C.DO
While the plasticizer content (ml) of the sheet using P decreased by about 40%, the weight loss of the sheet containing a high molecular weight polyester plasticizer was only about 2.3 weight at most.

(実施例1) 市販のポリjB化ビニル(重合度1300)100重量
部に対し市販の25℃にお(Jる結電が6500t?ン
テボアズのポリエステル系可塑剤(商品名[アデカサイ
ザーPN280j)を70重量部、バリウム−亜鉛系安
定剤3重量部、エポキシ化大豆油3重量部、紫外線吸収
剤0.1重量部、三酸化アンチモン3重量部、滑剤0.
5重量部を含む軟質塩化ビニル配合に、アルミニウム粉
末3重量部を加えた厚さ200ミクロンのシート(■)
と、同配合にアルミニウム粉末に代えてカーボンブラッ
ク3重量%を加えた厚さ350ミクロンのシート(II
)をカレンダー加工により成形し、この2種のシートを
熱ラミネートにより緊密に積層し、厚さ500ミクロン
のシルバー/ブラック2層積層シートを得た。
(Example 1) A commercially available polyester plasticizer (trade name: Adekasizer PN280j) was added to 100 parts by weight of commercially available polyjB vinyl (polymerization degree 1,300) at 25° C. 70 parts by weight, 3 parts by weight of barium-zinc stabilizer, 3 parts by weight of epoxidized soybean oil, 0.1 part by weight of ultraviolet absorber, 3 parts by weight of antimony trioxide, 0.0 parts by weight of antimony trioxide.
A 200 micron thick sheet made by adding 3 parts by weight of aluminum powder to a soft vinyl chloride formulation containing 5 parts by weight (■)
A sheet with a thickness of 350 microns (II
) was molded by calendering, and the two sheets were closely laminated by thermal lamination to obtain a silver/black two-layer laminate sheet with a thickness of 500 microns.

このシートをウェザリング試験機(スガ試験機製WE−
3UN−D、CA型)にか1ノ、ブラックパネル温石6
3±3℃、サンプルスプレー120分生18分の条件に
てシルバ一層が照射面になるようにして1000時間照
射を行った。
This sheet was tested using a weathering tester (WE- manufactured by Suga Test Instruments).
3UN-D, CA type) 1 no, black panel warm stone 6
Irradiation was carried out for 1000 hours at 3±3° C. and sample spray for 120 minutes and 18 minutes, with the silver layer being the irradiated surface.

照射後JIS K6723に準じ引張試験を行い脆化お
よび劣化の程度を顕著にあられす伸び残率を測定してと
ころ93%であった。ここで、伸び残率とは、照射前の
伸びに対づる照射後の伸びの割合である。以下の実施例
、比較例では脆化および劣化の程度を伸び残率で示す。
After irradiation, a tensile test was conducted according to JIS K6723, and the residual elongation rate, which indicates the degree of embrittlement and deterioration, was measured and found to be 93%. Here, the residual elongation rate is the ratio of the elongation after irradiation to the elongation before irradiation. In the following Examples and Comparative Examples, the degree of embrittlement and deterioration is expressed in terms of residual elongation.

(比較例1) 実施例1におけるアルミニウム粉末を加えた配合のみに
て厚さ500ミクロンのシルバー色単層シートを同じく
カレンダー加工により作成し、実施例1と同様に耐候性
試験を行った。
(Comparative Example 1) A silver-colored single-layer sheet with a thickness of 500 microns was prepared by calendering using only the formulation in Example 1 with the addition of aluminum powder, and a weather resistance test was conducted in the same manner as in Example 1.

1000時間射後の伸び残率は65%であった。The residual elongation rate after 1000 hours of irradiation was 65%.

(実施例2) 市販のエチレン−塩化ビニル共重合樹脂(重合度150
0、エチレン含量1.5%)100重間部に対し、市販
ポリエステル系可塑剤(商品名[アデカサイザーPN2
50J )を50市θ部、トリメリット酸オクチルエス
テル10市ffi部、バリ「クムー亜鉛系安定剤2.5
重品部および滑剤0.5重量部を含む軟質塩化ビニル配
合にアルミニウム粉末3型ω部、紫外線吸収剤0.1r
li部を加えた厚さ250ミクロンのシートと同配合に
アルミニウム粉末代えてカーボンブラック2ΦV%を加
えた厚さ300ミクロンのシートをカレンダー加工によ
り成形し、この2種のシートを熱ラミネート法により緊
密に積層し、斥さ500ミクロンの2層積層シートを得
た。
(Example 2) Commercially available ethylene-vinyl chloride copolymer resin (degree of polymerization 150
0, ethylene content 1.5%), commercially available polyester plasticizer (trade name [Adekasizer PN2
50J), 50 parts θ, 10 parts ffi trimellitic acid octyl ester, 2.5 parts Kumu zinc stabilizer
A soft vinyl chloride formulation containing heavy parts and 0.5 parts by weight of lubricant, aluminum powder type 3 ω part, and 0.1r ultraviolet absorber.
A sheet with a thickness of 250 microns with the li part added and a sheet with a thickness of 300 microns with the same composition but with carbon black 2ΦV% added instead of aluminum powder were formed by calendering, and these two sheets were tightly laminated using a thermal lamination method. A two-layer laminated sheet with a repulsion of 500 microns was obtained.

このシートを実施例と同様に耐候性試験を行った。This sheet was subjected to a weather resistance test in the same manner as in the examples.

1000時間照射後の伸び残率は92%であった。The residual elongation rate after 1000 hours of irradiation was 92%.

(実施例3) 市販のポリ塩化ビニル(重合度1000)100重量部
に対し、市販のポリ1ニスデル可塑剤(アデカリイザー
PN280)を35重量部、DOP25重量部、バリウ
ム−亜鉛系安定剤3重量部、エポキシ樹脂4重間部、紫
外線吸収剤0.2重量部、三酸化アンチ七ン3重量部、
滑剤0.5重量部およびアルミニウム粉末3型都部を含
む軟質塩化ビニル配合にて厚さ200ミクロンのシート
をカレンダ加■により成形した。またポリ塩化ビニル(
重合1復1000)1(’)0重量部に対しDOP 4
5部、バリウlオー亜鉛系安定剤3小吊部」−ポキシ化
大Ω油3重量部、三酸化アンチ[ン3小ω部、滑剤(1
,5重量部おにび醸化チタ重量市量%を含む軟質塩化ビ
ニル配合にて厚さ300ミクロンのシー]−をカレンダ
ー加1−により成形した。
(Example 3) To 100 parts by weight of commercially available polyvinyl chloride (degree of polymerization 1000), 35 parts by weight of commercially available poly 1 Nisder plasticizer (Adekarizer PN280), 25 parts by weight of DOP, and 3 parts by weight of barium-zinc stabilizer. , epoxy resin quadruple part, ultraviolet absorber 0.2 parts by weight, antiseptane trioxide 3 parts by weight,
A sheet with a thickness of 200 microns was formed by calendering using a soft vinyl chloride formulation containing 0.5 parts by weight of a lubricant and aluminum powder Type 3. Also, polyvinyl chloride (
DOP 4 for polymerization 1 to 1000) 1 (') 0 parts by weight
5 parts, 3 parts by weight of barium-ol-zinc stabilizer - 3 parts by weight of poxidized large Ω oil, 3 parts by weight of antitin trioxide, lubricant (1 part)
A sheet of 300 microns thick was molded by calendering 1-, using a soft vinyl chloride formulation containing 5 parts by weight of rice-brewed titanium (market weight).

この2種のシートを熱ラミネ−1〜にJ、り緊密に積層
し、厚さ/150ミクロンのシルバー/ホゾ182層積
層シートを得た。
These two types of sheets were closely laminated on thermal laminate 1 to obtain a silver/tenon 182-layer laminated sheet with a thickness of 150 microns.

このシー]・を温石100 ℃のもとで27IO時間加
熱した後実施例1と同様に耐候↑11試験を行った。
This material was heated at 100° C. for 27 IO hours, and then subjected to weathering test ↑11 in the same manner as in Example 1.

1oontrt間照1)J後の伸び残率は98%l・あ
った。
The residual elongation rate after 1 oon trt 1) J was 98%l.

(比較例2) 市販のポリ塩化1″″ニル(重合度1000)100重
間部に対し、[10P6n重量部、バリ1クム一曲鉛系
安定剤3小量部、紫外線吸収剤0.1重量部、三酸化ア
ンチモン3重1部を含むポリ塩化ビニル軟質配合にアル
ミニウム粉末2重量部を加えた厚み200ミクロンのシ
ー]−と、アルミニウム粉末に代えてカーボンブラック
3重量%を加えた厚み350ミクロンのシートをカレン
ダー加工により成形し、この2種のシートを熱ラミネー
ト法にJ:り積層し、厚さが500ミクロンのシルバー
/ブラック2層積層シー1−を得た。
(Comparative Example 2) For 100 parts by weight of commercially available polychloride 1''nyl (degree of polymerization 1000), [10P6n parts by weight, 1 cum of flash, 3 small parts of curved lead stabilizer, and 0.1 part of ultraviolet absorber. 2 parts by weight of polyvinyl chloride soft formulation containing 3 parts by weight, 1 part by weight of antimony trioxide plus 2 parts by weight of aluminum powder, and a thickness of 350 microns by adding 3 parts by weight of carbon black in place of the aluminum powder. A micron sheet was formed by calendering, and the two types of sheets were laminated using a thermal lamination method to obtain a silver/black two-layer laminated sheet 1- with a thickness of 500 microns.

このシートを温度100℃のもとて240時間加熱した
のち実施例1と同様に耐候性試験を行った。
After this sheet was heated at a temperature of 100° C. for 240 hours, a weather resistance test was conducted in the same manner as in Example 1.

1000時間照射後の伸び残率を測定したところ30%
であった。
The residual elongation rate after 1000 hours of irradiation was 30%.
Met.

(比較例3) 比較例2におけるアルミニウム粉末を加えた配合のみに
て厚ざ500ミクロ、ンのシルバー色単層シートをカレ
ンダー加工にて作成し、実施例1と同様に耐候性試験を
行った。
(Comparative Example 3) A silver-colored single-layer sheet with a thickness of 500 micrometers was prepared by calendering using only the formulation in which aluminum powder was added in Comparative Example 2, and a weather resistance test was conducted in the same manner as in Example 1. .

1000時間照射後の伸び残率は43%であった。The residual elongation rate after 1000 hours of irradiation was 43%.

(実施例4) 市販のポリ塩化ビニル(重合11000)100重fM
にポリエステル系iT塑剤(アデカサイザーPN280
)を70重量部、バリウム−亜鉛系安定剤2.5重量部
、エポキシ大豆油3重量部、紫外線吸収剤0.1重量部
、三酸化アンチモン3重量部、を含む軟質配合にアルミ
ニウム粉末3重量部を含む厚さ200ミク[1ンのシー
1〜とアルミニウム粉末に代えてカーボンブラック3重
量%を含む250ミクロンのシートをカレンダー法によ
り作成し、この2種のシー1へを熱ラミネート法ににり
積層し厚さ400ミクロンのシルバー/ブラック積層シ
ートを得た。
(Example 4) Commercially available polyvinyl chloride (polymerization 11000) 100 fM
polyester iT plasticizer (ADEKASIZER PN280)
), 2.5 parts by weight of barium-zinc stabilizer, 3 parts by weight of epoxy soybean oil, 0.1 part by weight of ultraviolet absorber, 3 parts by weight of antimony trioxide, and 3 parts by weight of aluminum powder. A 250 micron sheet containing 200 μm thick [1 ml] and 3 wt. A silver/black laminated sheet having a thickness of 400 microns was obtained by laminating the silver/black laminated sheet.

このシートを1〔21℃、168時間加熱し加熱後の重
量減少%を測定したどころ2%であった。
This sheet was heated at 21° C. for 168 hours, and the weight loss after heating was measured to be 2%.

このシーi−の加熱処理後の伸び残率を測定したところ
98%であった。
The residual elongation rate of this Sea I- after heat treatment was measured and found to be 98%.

(実施例5) 実施例4の配合のうちポリエステル系可塑剤(PN28
0)をト・リメリツ1へ酸オクチルエステル(アデカリ
イザーC−8)に代えて実施例4と同一の加工を行い厚
さ400ミクロンのシルバー/ブラック2層積層シート
を作成した。このシートを実施例4と同様の熱処理を行
い加熱後の重量減少%を測定したところ1%であった。
(Example 5) Polyester plasticizer (PN28
A silver/black two-layer laminate sheet having a thickness of 400 microns was prepared by carrying out the same processing as in Example 4 except that Trimeriz 1 (Adekalizer C-8) was used instead of Trimeriz 1 (Adekarizer C-8). This sheet was heat treated in the same manner as in Example 4, and the weight loss percentage after heating was measured, and it was 1%.

このシートの実施例4と同一条件での加熱処理後の伸び
残率を測定したところ97%であった。
The residual elongation of this sheet after heat treatment under the same conditions as in Example 4 was measured and found to be 97%.

(比較例4) 実施例4の配合のうちポリエステル系可塑剤(PN28
0)70重量部をDOP50重in部重度n部実施例4
と同様の加■を行い厚さ4ooミクロンのシルバー/ブ
ラック2層積層シートを作成した。
(Comparative Example 4) Among the formulations of Example 4, polyester plasticizer (PN28
0) 70 parts by weight of DOP 50 parts by weight n parts Example 4
A silver/black two-layer laminate sheet having a thickness of 40 microns was prepared by carrying out the same process as described above.

このシートを実施例4と同様の熱処理を行い加熱後の重
量減少%を測定したところ30%であった。
This sheet was subjected to the same heat treatment as in Example 4, and the weight loss percentage after heating was measured and found to be 30%.

このシートの加熱処理後の伸び残率を測定したところ0
%であった。
The residual elongation rate of this sheet after heat treatment was measured and was 0.
%Met.

(実施例6) 市販のポリ塩化ビニル(重合1’fl 300)50重
間%とエチレン/塩化ビニル共重合樹脂(重合度150
0.y−チレン含量、1.5重量%)50重量%とのブ
レンド物100重闇部にポリニスデル系可塑剤(アデカ
4)−イザーPN280>500重量、r)OPIO重
聞部、バリウム−叶鉛系安定剤3重量部、三酸化アンチ
モン3重量部を含む軟質塩化ビニル配合にアルミニウム
粉3市出部を加えた厚さ250ミク[1ンのシートとア
ルミニウム粉末に代えてカーボンブラック5重量%を加
えた厚さ300ミクロンのシートをカレンダー加工によ
り作成し、熱ラミネーターにより両シートを緊密に張り
合わせ厚さ500ミク[1ンのシルバー/ブラック2層
積層シー1〜を作成した。
(Example 6) Commercially available polyvinyl chloride (polymerization 1'fl 300) 50% by weight and ethylene/vinyl chloride copolymer resin (polymerization degree 150)
0. y-tyrene content, 1.5% by weight) blend with 50% by weight polynisder plasticizer (ADEKA 4) - Iser PN280 > 500% by weight, r) OPIO heavy part, barium-lead system A soft vinyl chloride formulation containing 3 parts by weight of stabilizer and 3 parts by weight of antimony trioxide was added with 3 parts of aluminum powder to a thickness of 250 μm [1 inch sheet and 5% by weight of carbon black was added in place of the aluminum powder. A sheet with a thickness of 300 microns was prepared by calendering, and both sheets were laminated tightly using a heat laminator to prepare a silver/black two-layer laminated sheet 1~ with a thickness of 500 microns.

このシー1−を幅10CI11のテープ状に切り出し、
屋外のパイプラック状の蒸気配管にケイ酸カルシウム成
型保温剤を配管外周に沿って巻きつけ針金で固定し、こ
の外装(直径約150m) 、にテープ状にした当該2
層外装材をシルバ一層を外側にして包帯を巻く要領で約
2Cm幅で単>rるようにきつく巻きつけ端部を両面粘
着テープにて接合し、更にその上からバンド状の金具に
て占めつけて固定した。 2年粁過後この外装の状態を
調べたが、若干表面が汚れ黒味があったが、亀裂、切断
などの以上は何らみられず、ざらに使用ir能の状態で
あった。
Cut this sheet 1- into a tape shape with a width of 10CI11,
A calcium silicate molded heat insulator was wrapped around the outer circumference of an outdoor pipe rack-shaped steam pipe and fixed with wire, and this exterior (approximately 150 m in diameter) was covered with tape.
Wrap the layered exterior material tightly with the silver layer on the outside in a manner similar to wrapping a bandage to a width of about 2 cm, and join the ends with double-sided adhesive tape, then cover with a band-shaped metal fitting from above. I attached it and fixed it. After 2 years of aging, the condition of the exterior was examined, and although the surface was slightly dirty and blackish, there were no cracks or cuts, and it was in roughly usable IR-capable condition.

2年使用後のシー1へを切りとり、引張特性を測 24
一 定したところ、引張強さ、伸び共に95%の保持率を示
した。
Cut out Sea 1 after 2 years of use and measure the tensile properties 24
When stabilized, both tensile strength and elongation showed a retention rate of 95%.

(比較例5) 実施例7と同じ外装を市販の防蝕軟質ポリ塩化ヒニルテ
ープを用いて実施例7ど同じ方法にて巻きつけ比較を行
った。
(Comparative Example 5) A comparison was made by wrapping the same exterior as in Example 7 using a commercially available corrosion-resistant soft polyhinyl chloride tape in the same manner as in Example 7.

2年経過後防蝕デープは上面の部分より亀裂が入り切断
が生じはじめ使用に絶えない状態となった。
After two years, the corrosion-resistant tape began to crack and break from the upper surface, making it unusable.

(実施例7) 市販のポリ塩化ビニル(重合度1000)100重最重
量、ジペンタエリスリトールエステル可塑剤アデカサイ
ザーUL−6)55重量部にDOPIO重量部、バリウ
ム−111i鉛系安定剤2.5重量部、■ポキシ大豆油
3ff1Mi部、紫外線吸収剤(テヌビンP)0.1重
量部、アルミニウム粉末3重間部を含む厚さ200ミク
ロンのシート(I)どアルミニウム粉末に代えカーボン
ブラック3重量%を含むシート(I)と同配合の厚さ3
00ミクロンのシート(II)をカレンダー法により作
成し、シート(T)および(II)とを熱ラミネート法
により積層し厚さ500ミクロンのシルバー/ブラック
積層シートを得た。この積層シートを実施例4と同一条
件で試験したところ重量減少率は2.7%であった。又
、加熱処理後の伸び残率は92%であった。
(Example 7) Commercially available polyvinyl chloride (degree of polymerization 1000) 100 weight, dipentaerythritol ester plasticizer Adekasizer UL-6) 55 parts by weight, DOPIO parts by weight, barium-111i lead stabilizer 2.5 parts by weight parts by weight, ■ 3ff1Mi part of poxy soybean oil, 0.1 part by weight of ultraviolet absorber (Tenuvin P), 200 micron thick sheet (I) containing a triple layer of aluminum powder, and 3% by weight of carbon black in place of the aluminum powder. Thickness 3 of the same composition as sheet (I) containing
A sheet (II) with a thickness of 0.00 microns was prepared by a calendering method, and sheets (T) and (II) were laminated by a thermal lamination method to obtain a silver/black laminated sheet with a thickness of 500 microns. When this laminated sheet was tested under the same conditions as in Example 4, the weight reduction rate was 2.7%. Further, the residual elongation rate after the heat treatment was 92%.

(実施例8) 実施例1に記載の厚さ200ミクロンのシート(T)と
酢酸ビニル含ff1321iFJ%、メルトインデック
ス30g/10分の■チレンー酢酸ビニル共重合体(F
VA)53重間%を含む塩化ビニル−IE V Aグラ
フト共重合体(塩ビ部の平均重合度800)100重閤
重重バリウム−4F鉛系安定剤2.5重量部、■ポキシ
大豆油3重量部及びカーボンブラック3重量%を含む厚
ざ300ミクロンのシート(II)とを熱ラミネー1〜
法により積層し、厚さ500ミクロンのシルバー719
99Mlシートを得た。この積層シートを実施例1と同
一試験条件で試験したところ伸び残率は94%であった
(Example 8) The sheet (T) with a thickness of 200 microns described in Example 1 and the tyrene-vinyl acetate copolymer (F
VA) Vinyl chloride-IE V A graft copolymer containing 53% by weight (average degree of polymerization of the vinyl chloride part 800) 100% by weight barium-4F lead stabilizer 2.5 parts by weight, 3 parts by weight of poxy soybean oil and a sheet (II) having a thickness of 300 microns containing 3% by weight of carbon black.
500 micron thick silver 719
A 99Ml sheet was obtained. When this laminated sheet was tested under the same test conditions as Example 1, the residual elongation rate was 94%.

Claims (1)

【特許請求の範囲】[Claims] (1)重合度が650以上のポリ塩化ビニル系樹脂10
0重量部に、一種または二種以上の下記から選ばれる低
揮発性耐熱可塑剤を少なくとも40重量%以上含む可塑
剤20〜80重量部、着色剤およびポリ塩化ビニル系樹
脂に通常使用される安定剤を添加した、厚さが50ミク
ロンから 1000ミクロンの外部可塑化軟質塩化ビニル系樹脂シ
ート(I)と、重合度が650以上のポリ塩化ビニル系
樹脂100重量部に、特に種類を選ばない可塑剤0〜8
0重量部、ポリ塩化ビニル系樹脂に通常使用される安定
剤および少なくとも0.5重量%以上のカーボンブラッ
ク及び/又は酸化チタンを添加した、厚さが50ミクロ
ンから1600ミクロンの内部又は外部可塑化軟質塩化
ビニル系樹脂シート(II)を熱融着によって一体に接合
してなる、厚さが100ミクロンから1700ミクロン
の外装用軟質塩化ビニル系樹脂テープ。 i)粘度が250cp/25℃以上の飽和ポリエステル
系可塑剤、 ii)粘度が80cp/25℃以上のトリメリット酸エ
ステル、エポキシ化大豆油、エポキシ化あまに油、 iii)粘度が100cp/25℃以上のエポキシ化脂
肪酸エステル系可塑剤、 iv)分子量が400以上のフタル酸系、テトラヒドロ
フタル酸系、アジピン酸系、アゼライン酸系、セバシン
酸系、クエン酸系、リン酸系可塑剤、v)テトラ−2−
エチルヘキシルピロメリテート、テトラ−n−オクチル
ピロメリテートのピロメリット酸エステル系可塑剤、 vi)ジペンタエリスリトール、ペンタエリスリトール
エステル系可塑剤。
(1) Polyvinyl chloride resin 10 with a degree of polymerization of 650 or more
0 parts by weight, 20 to 80 parts by weight of a plasticizer containing at least 40% by weight of one or more low-volatility heat-resistant plasticizers selected from the following, a coloring agent, and a stabilizer commonly used for polyvinyl chloride resins. An externally plasticized soft vinyl chloride resin sheet (I) with a thickness of 50 to 1000 microns and 100 parts by weight of a polyvinyl chloride resin with a degree of polymerization of 650 or more, with any type of plasticizer added Agent 0-8
0 parts by weight, with the addition of stabilizers commonly used in polyvinyl chloride resins and at least 0.5% by weight of carbon black and/or titanium oxide, internally or externally plasticized with a thickness of 50 microns to 1600 microns. A soft vinyl chloride resin tape for exterior use with a thickness of 100 to 1700 microns, which is made by bonding soft vinyl chloride resin sheets (II) together by heat fusion. i) A saturated polyester plasticizer with a viscosity of 250 cp/25°C or higher, ii) Trimellitic acid ester, epoxidized soybean oil, or epoxidized linseed oil with a viscosity of 80 cp/25°C or higher, iii) A viscosity of 100 cp/25°C iv) Phthalic acid-based, tetrahydrophthalic acid-based, adipic acid-based, azelaic acid-based, sebacic acid-based, citric acid-based, phosphoric acid-based plasticizers with a molecular weight of 400 or more; v) Tetra-2-
pyromellitic acid ester plasticizers such as ethylhexylpyromellitate and tetra-n-octylpyromellitate; vi) dipentaerythritol and pentaerythritol ester plasticizers.
JP60109412A 1985-05-23 1985-05-23 Flexible vinyl chloride group resin tape for sheathing Granted JPS61268445A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60109412A JPS61268445A (en) 1985-05-23 1985-05-23 Flexible vinyl chloride group resin tape for sheathing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60109412A JPS61268445A (en) 1985-05-23 1985-05-23 Flexible vinyl chloride group resin tape for sheathing

Publications (2)

Publication Number Publication Date
JPS61268445A true JPS61268445A (en) 1986-11-27
JPH0263062B2 JPH0263062B2 (en) 1990-12-27

Family

ID=14509590

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60109412A Granted JPS61268445A (en) 1985-05-23 1985-05-23 Flexible vinyl chloride group resin tape for sheathing

Country Status (1)

Country Link
JP (1) JPS61268445A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000007866A (en) * 1998-06-19 2000-01-11 Tatsuno Kagaku:Kk Non-adhesive tape for protecting and displaying pipe and its production
JP2008006605A (en) * 2006-06-27 2008-01-17 Mitsubishi Plastics Ind Ltd Vinyl chloride type laminated/stretched film and its manufacturing method
JP2011521801A (en) * 2008-05-01 2011-07-28 サンゴバン・パフォーマンス・プラスティックス・コーポレーション Multi-layer fuel pipe
WO2022190808A1 (en) * 2021-03-08 2022-09-15 デンカ株式会社 Adhesive tape and air conditioner pipe

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000007866A (en) * 1998-06-19 2000-01-11 Tatsuno Kagaku:Kk Non-adhesive tape for protecting and displaying pipe and its production
JP2008006605A (en) * 2006-06-27 2008-01-17 Mitsubishi Plastics Ind Ltd Vinyl chloride type laminated/stretched film and its manufacturing method
JP2011521801A (en) * 2008-05-01 2011-07-28 サンゴバン・パフォーマンス・プラスティックス・コーポレーション Multi-layer fuel pipe
WO2022190808A1 (en) * 2021-03-08 2022-09-15 デンカ株式会社 Adhesive tape and air conditioner pipe

Also Published As

Publication number Publication date
JPH0263062B2 (en) 1990-12-27

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