JPS58208016A - Manufacture of tile made of synthetic resin - Google Patents

Manufacture of tile made of synthetic resin

Info

Publication number
JPS58208016A
JPS58208016A JP9037682A JP9037682A JPS58208016A JP S58208016 A JPS58208016 A JP S58208016A JP 9037682 A JP9037682 A JP 9037682A JP 9037682 A JP9037682 A JP 9037682A JP S58208016 A JPS58208016 A JP S58208016A
Authority
JP
Japan
Prior art keywords
synthetic resin
vinyl chloride
parts
polymer
weight
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
JP9037682A
Other languages
Japanese (ja)
Other versions
JPS6234342B2 (en
Inventor
Norio Oribe
織部 法雄
Tatsuo Kobayashi
達雄 小林
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.)
Nitto Boseki Co Ltd
Original Assignee
Nitto Boseki 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 Nitto Boseki Co Ltd filed Critical Nitto Boseki Co Ltd
Priority to JP9037682A priority Critical patent/JPS58208016A/en
Publication of JPS58208016A publication Critical patent/JPS58208016A/en
Publication of JPS6234342B2 publication Critical patent/JPS6234342B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C43/00Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor
    • B29C43/22Compression moulding, i.e. applying external pressure to flow the moulding material; Apparatus therefor of articles of indefinite length
    • B29C43/24Calendering
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/06Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
    • B29K2105/12Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts of short lengths, e.g. chopped filaments, staple fibres or bristles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/10Building elements, e.g. bricks, blocks, tiles, panels, posts, beams
    • B29L2031/104Tiles

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To strengthen the paste directed for calender roll-forming by using rock wool or wallastonite having specially determined fiber length together with acryl series synthetic resin composed of formability-improving agent instead of asbestos used as reinforcing material for synthetic resin tile. CONSTITUTION:100pts.wt. parts of the synthetic resin chosen from the group of vinyl chloride series polymer, vinyl chloride-vinyl acetate polymer or ethylene- vinyl chloride polymer, 40-55pts.wt. parts of plasticizer, 3-7pts.wt. parts of stabilizer, 15-25pts.wt. parts of rosin denatured resin or petroleum denatured resin, 400-700pts.wt. parts of calcium carbonate, 40-150pts.wt. parts of rock wool with under 700mum fiber length or wallastnite and 4-10pts.wt. parts of acryl series synthetic resin composed of formability-improving agent for vinyl chloride synthetic resin are mixed. After this mixed composition is sufficiently kneaded with mixing by a closed pressurized kneading machine and is made into a sheet by a mixing roll, it is finished at determined thickness by a calendar roll.

Description

【発明の詳細な説明】 本発明は、塩化ビニルIF合体、塩化ビニルー酢酸ビニ
ル共東合体、エチレン−塩化ビニル共重合体等よりなる
合成樹脂を利用したカレンダーロール方式による合成樹
脂製タイルの製造方法に関するものであり、従来のカレ
ンダロール方式による塩化ビニル系合成樹脂製タイルの
製造にお℃・て必須不可欠な成分とされていた石綿を使
用することなく、従来の、石綿を使用したカレンダーロ
ール方式で得られた塩化ビニル系合成樹脂製タイルが有
する諸性状に比較して何ら遜色のない塩化ビニル系合成
樹脂製タイルを、カレンダーロール方式にて効率良く得
る方法を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for producing synthetic resin tiles using a calendar roll method using synthetic resins such as vinyl chloride IF combination, vinyl chloride-vinyl acetate copolymer, and ethylene-vinyl chloride copolymer. It is related to the conventional calender roll method that uses asbestos, without using asbestos, which is an essential ingredient in the production of vinyl chloride synthetic resin tiles using the conventional calender roll method. The object of the present invention is to provide a method for efficiently obtaining vinyl chloride-based synthetic resin tiles, which have properties comparable to those of the vinyl chloride-based synthetic resin tiles obtained in the above, using a calendar roll method.

塩化ビニル重合体、塩化ビニルー酢酸ビニル共屯合体、
エチレン−塩化ビニル共重合体等(以下塩化ビニル系重
合体と略称する)を使用した合成樹脂製タイルの製造方
法には、合成樹脂とその他の添廂物との混合組成物の混
練物をミキシングロールでシート化し、次いでカレンダ
−ロールで所定の厚さに仕上げるカレンダーロール方式
と、合成樹脂とその他の添加物との混合組成物をプレス
成形に付し、シート状成形体に成形するプレス成形方式
とがある。
Vinyl chloride polymer, vinyl chloride-vinyl acetate copolymer,
The method for manufacturing synthetic resin tiles using ethylene-vinyl chloride copolymer (hereinafter referred to as vinyl chloride polymer) involves mixing a kneaded mixture of a synthetic resin and other additives. A calendar roll method in which the sheet is formed into a sheet using rolls and then finished to a predetermined thickness with a calender roll, and a press molding method in which a mixed composition of synthetic resin and other additives is press-molded to form a sheet-like molded product. There is.

ところが、前りのカレンダーロール方式ニおいては、カ
レンダーロール成形に付される混線物が成る程度以1−
の強度を有していなければならtl:<、このた、−′
)の補強材として、従来、石綿を、塩イしビニル系1n 程度添加,混合使用することが必須不可欠な要件とされ
て(・ろが、石綿が及ぼす公害上の問題、取扱い名への
健康I−の悪影響等が明C)かにされている現在、こ(
り石綿を使用するカレンダーロールツノ式による地化ビ
ニル系合成樹脂製タイルの製造lJ′θ、は、公害面で
、また操業者の健康管理の而で、諸種問題があるばかり
でなく、石綿自体の資源枯渇に伴い価格がト昇する傾向
にあり、製品価格が高騰すると(・う欠点をも有して(
・る。
However, in the previous calender roll method, the amount of contaminants added to the calender roll formation is 1-1.
It must have an intensity of tl:<, this, −′
) As a reinforcing material, it has been considered essential to add and mix asbestos with about 1n of vinyl salt. Now that the negative effects of I- have been made clear, this (C)
The production of polyvinyl synthetic resin tiles using the calender roll horn method using asbestos not only poses various problems in terms of pollution and health management of operators, but also produces asbestos itself. With the depletion of resources, prices tend to rise, and when product prices soar,
・Ru.

また、後者のプレス成形方式は、その成形工程上で、特
に成形段階にある混合組成物に特定の物性が必要とさね
な(・ので、カレンダーロール11式において必須不u
J欠とされている石綿を使用することなく成形を行うこ
とが出来ろことから、石綿の使用に伴う前述のような欠
点はな(・が・前者のカレンダーロール方式に比較して
成形速度が著しく遅く、生産効率の点で問題がある。
In addition, the latter press molding method requires specific physical properties for the mixed composition in the molding stage, so the 11 types of calender rolls require certain physical properties.
Since it is possible to perform molding without using asbestos, which is considered to be deficient, there are no disadvantages as mentioned above associated with the use of asbestos (although the molding speed is slower than the former calender roll method). It is extremely slow and has problems in terms of production efficiency.

本発明は肪−11′I請求の範囲に記載した構成とする
ことにより、従来のカレンダーロール11式による塩化
ビニル系合成樹脂製タイルの製造にお□ いて必須不II■欠な成分とされている石綿を使用する
ことなく、従来の成形Jiθ、で得られる塩化ビニル系
合成樹脂製タイルが具備する諸性状に比較して何ら遜〔
aのない塩化ビニル系合成樹脂製タイルを、生IYf゛
効率の高いカレンダーロールJj“式にて得ろJJ’ 
r.J、を提供するもので、従来の塩1ヒビニル系合成
樹脂製タイルの製造方法におけろ欠点を悉く解消するも
のである。
By adopting the structure described in the claims of the present invention, fat-11'I can be used as an essential component in the production of vinyl chloride synthetic resin tiles using the conventional calender roll 11 system. The properties are in no way inferior to those of vinyl chloride synthetic resin tiles obtained by conventional molding without using asbestos.
A-free vinyl chloride synthetic resin tiles can be obtained using the highly efficient calender roll method JJ'
r. J, which eliminates all the drawbacks of the conventional method for producing tiles made of vinyl salt-based synthetic resin.

以ト本発明の塩化ビニル系合成樹脂製タイルの製造方法
の構+,Qについて説明する1、+:発明の塩化ビニル
系合成樹脂製タイルの製造方rJ=は、塩化ビニル重合
体,塩化ビニルー酢酸ビニル共東合体、またはエチレン
−塩化ビニルJいF合体の中から選択される合成樹脂1
00Φ:I:部と、可塑i’jll ’I O〜3 5
 ffl敬部と、安定剤3へ7屯)を1部と、ロジン変
性樹脂または石油変性樹脂/S〜λ、ダΦ゛騎部と、炭
酸力/Lシウムqθθ・〜70θ中針部と、繊維長70
θμ以ドの11ツクウー/l(好ましくは非繊維状物を
含まない長さ300μ以ドのもの)またはウオラストナ
イト11・qO〜/ !;O!ff量部と、塩置部ニル
系合成樹脂の加工性改良剤たるアクリル系合成樹脂q〜
70型破部との混合組成物を、密閉式加圧混練機を用い
て良く混練し、得られた混練物をミキシングロールで7
ート化した後、次いでカレンダーロールで所定の厚さに
仕上げるもので、補強材として使用されていた石綿の代
りに、繊維長2Sθμ以下のロックウールまたはウオラ
ストナイトと塩化ビニル系樹脂の加工性改良剤たるアク
リル系合成樹脂とを併用することにより、カレンダーロ
ール成形に付される混練物に、該混練物に必要とされる
強度を具備せしめるものである、。
Hereinafter, the structure + and Q of the method for producing a vinyl chloride synthetic resin tile of the present invention will be explained. 1, +: The method for producing a vinyl chloride synthetic resin tile of the invention Synthetic resin 1 selected from vinyl acetate combination or ethylene-vinyl chloride JF combination
00Φ:I: part and plastic i'jll'I O~3 5
1 part of rosin-modified resin or petroleum-modified resin/S~λ, daΦ゛kibe, carbonic power/L sium qθθ・~70θ central needle part, Fiber length 70
11 qO/l of less than θμ (preferably one with a length of 300μ or more that does not contain non-fibrous materials) or wollastonite 11·qO~/! ;O! ff amount part and salt storage part acrylic synthetic resin q~ which is a processability improver for nil-based synthetic resin
The mixed composition with the 70-mold broken part was well kneaded using a closed pressure kneader, and the resulting kneaded product was mixed with a mixing roll for 70 minutes.
After forming into a sheet, it is finished to a specified thickness using calender rolls, and instead of asbestos used as a reinforcing material, rock wool or wollastonite with a fiber length of 2Sθμ or less and vinyl chloride resin are used. By using the acrylic synthetic resin as a modifier, the kneaded material subjected to calender roll molding is provided with the strength required for the kneaded material.

次に本発明の塩化ビニル系合成樹脂製タイルの製造方法
において、塩化ビニル系重合体に添加使用される各□成
分について説明する。
Next, each component added to the vinyl chloride polymer in the method for manufacturing a vinyl chloride synthetic resin tile of the present invention will be explained.

fll  aT塑剤 主としてフタル酸系可塑剤が使用される。fll aT plasticizer Primarily phthalic acid plasticizers are used.

塩化ビニル系重合体700重量部に対する可塑剤の使用
量か≠θ重警部未満の場合には。
If the amount of plasticizer used per 700 parts by weight of vinyl chloride polymer is less than θ.

jIIられる合成樹脂製タイルに柔軟性がなく硬くなり
すぎるシ1、また、55重量部を越えると、得られる合
成樹脂製タイルが柔らかくなりすぎるので、可塑剤は塩
化ビニル系重合体の9θ〜55重量%の範囲内で添加さ
れる。
j II The resulting synthetic resin tile will be inflexible and too hard. If the amount exceeds 55 parts by weight, the resulting synthetic resin tile will become too soft. It is added within a range of % by weight.

(21安定剤 塩化ビニル糸重合体に対する安定剤が使用されることが
勿論であるが、主として脂肪酸カルボン酸金属石ケンや
有機金属化合物が利用される。塩化ビニル系重合体10
0重量部に対する安定剤の使用量が3重世部未満では、
安定剤混合の効果が少なく、また7重量部を越える場合
には、安定剤増量による効果がその割合には十ケ1しな
いので、安定剤は塩化ビニル系重合体の3〜7重量%の
範囲内で添加される。
(21 Stabilizers Of course, stabilizers for vinyl chloride yarn polymers are used, but fatty acid carboxylic acid metal soaps and organometallic compounds are mainly used. Vinyl chloride polymers 10
If the amount of stabilizer used per 0 parts by weight is less than 3 parts by weight,
The effect of mixing the stabilizer is small, and if it exceeds 7 parts by weight, the effect of increasing the amount of stabilizer will not be as good as that ratio, so the stabilizer should be in the range of 3 to 7% by weight of the vinyl chloride polymer. Added within.

(3) ロジン変性樹脂または石油変性樹脂口、ジン変
性樹脂または石油変性樹脂は、塩化ビニル系重合体とそ
の他の添加物との混線物を、ミキシングロールで7−ト
化する際に、混線物に粘着性を発現させ、ミキシングロ
ールによるソート化を円滑に進める作用を果させるもの
で、松ヤニやトール油より採取されるロジンをエステル
化あるいはライノ・化し、更に用途に応じて金属塩等を
付加させたロジン変性樹脂、あるいは同様に、石油樹脂
をエステル化あるいはライム化し、更に必要に応じて金
属塩等を付加させた石油変性樹脂が使用される。、塩化
ビニル系重合体700重蒙部に対するロジン変性樹脂ま
たは石油変性樹脂の使用量が75重量部未満では、混練
物の発現する粘着性が十分ではなく、ロジン変性樹脂ま
たは石油変性樹脂添加の効果が得られないし、また25
重計部を越えると混線物の粘着性が大きくなりすぎるた
めに、ミキシングロールによる/−ト化の際に混練物が
ロールにねばり付き、シート化の成形工程が円滑にゆか
なくなるので、ロジン変性樹脂または石油変性樹脂は塩
化ビニル系重合体の15〜a2 !; +(f ii%
の範囲内で添加される。
(3) Rosin-modified resin, petroleum-modified resin, gin-modified resin, or petroleum-modified resin are used to create a mixture of vinyl chloride polymer and other additives when mixed with a mixing roll. This product develops stickiness and facilitates sorting using mixing rolls.Rosin, which is extracted from pine tar and tall oil, is esterified or rhino-ized, and metal salts are added depending on the application. A rosin-modified resin is used, or similarly, a petroleum-modified resin obtained by esterifying or liming a petroleum resin and further adding a metal salt or the like as necessary. If the amount of rosin-modified resin or petroleum-modified resin used is less than 75 parts by weight based on 700 parts by weight of the vinyl chloride polymer, the kneaded product will not have sufficient tackiness, and the effect of adding the rosin-modified resin or petroleum-modified resin will decrease. I can't get 25 again.
If it exceeds the weighing section, the stickiness of the mixed material will become too large, and the mixed material will stick to the roll when it is formed into sheets using a mixing roll, and the sheet forming process will not proceed smoothly. Resin or petroleum modified resin is 15~a2 of vinyl chloride polymer! ; +(f ii%
It is added within the range of

(1)  炭酸力ルンウノ、 炭酸カル/・′ツノ、は増琶剤として添加されるもので
あるが、塩化ビニル系重合体/ 00 ffiは部に対
して炭酸カルシウムが700重是重景越えると、?:j
られる塩化ビニル系合成樹脂製タイルが脆くなるので、
7θθ重社部以ドに抑えておくことが必要である。また
、llθθ市E化部未満でj−1、炭酸カルシウムの添
加が、混合(・(よるH科費の節約の効果が1−分では
なくなるので、1−としてSθ〜30θメツンユ程庇の
粉末状炭酸カルシウムが、塩化ビニル系1F合体の1l
oo〜700重量%の範囲内で添加される。。
(1) Calcium carbonate is added as a waxing agent, but when vinyl chloride polymer/00 ffi contains more than 700 parts of calcium carbonate, ,? :j
PVC-based synthetic resin tiles become brittle, so
It is necessary to keep it below 7θθ. In addition, if the addition of calcium carbonate is less than 1-1, the addition of calcium carbonate will be less than 1-min. Calcium carbonate is 1 liter of vinyl chloride-based 1F combined
It is added within the range of oo to 700% by weight. .

(5)  ロックウールまたはウオラストナイトロック
ウールまたはウオラストナイトは、いずれも、後述する
塩化ビニル系重合体による合成樹脂の加工性改良剤たる
アクリル系合成樹脂と相俟って、ミキシングロールによ
るシート化工程の混練物に、該混練物が必要とする強度
を具備させるもので、ロックウールの場合は繊維長70
0μ以下のものが使用できるが、特に非繊維状物を含ま
ない300μ以下のものが好ましく、更にはカップリン
グ剤等の表面処理剤で表面処理されたものは、流動性が
向−1−シ、塩化ビニル系合成樹脂や充填剤等の絡み作
用が良くなるので、より優れた結果が得られる、。
(5) Rock wool or wollastonite Both rock wool and wollastonite are used together with acrylic synthetic resin, which is a processability improver for synthetic resins made from vinyl chloride polymers, to be described later, to form sheets using mixing rolls. It gives the kneaded material in the oxidation process the strength required for the kneaded material, and in the case of rock wool, the fiber length is 70.
A material of 0μ or less can be used, but a material of 300μ or less that does not contain non-fibrous materials is particularly preferable.Furthermore, those that have been surface-treated with a surface treatment agent such as a coupling agent have a fluidity that is in the direction of -1-shield. , the entangling effect of vinyl chloride synthetic resins, fillers, etc. is improved, so better results can be obtained.

ロックウールの場合も、またウオラストナイトの場合も
、塩化ビニル系重合体700電値部に対してlIO重量
部未満だと、得られる混線物の補強効果が十分ではない
ばかりでなく、成形体である塩化ビニル系合成樹脂製タ
イルの・1゛法安定性が悪化するし、また、15゜Φ縫
部を越えると、得られる合成樹脂製タイl【が硬くて脆
くなるので、ロックウールまたはウオラストナイトは、
いずれの場合でも、塩化ヒニル糸小合体のllo〜/3
0重蓋チの範囲内で添加される。
In the case of rock wool and wollastonite, if the amount is less than 10 parts by weight relative to 700 parts by weight of the vinyl chloride polymer, not only will the reinforcing effect of the resulting mixed material be insufficient, but also the molded product will not have a sufficient reinforcing effect. The stability of vinyl chloride synthetic resin tiles deteriorates, and if the seam exceeds 15°Φ, the resulting synthetic resin tiles become hard and brittle, so do not use rock wool or wool. Last night is
In any case, llo~/3 of the hinyl chloride thread small coalescence
It is added within the range of 0.

(6) 塩化ビニル系樹脂の加工性改良剤たるアクリル
系合成樹脂 塩化ビニル系樹脂の加工性改良剤として市販されている
アクリル系樹脂がそのまま使用できる3、こfI Lj
、前述の繊維長7ooμ以下のロックウールまたはウオ
ラストナイトと相俟って、ミギ/ノグロールによる/−
ト化工程での混練物に、該混練物が必要とする強度を具
備させるもので、この塩化ビニル系合成樹脂の加工性改
良剤たるアクリル系合成樹脂の添加によって塩化ビニル
系合成樹脂のゲル化が速進され、増祉剤として添加され
ている炭酸力ルンウム等とのつなぎ効果が発現されるも
のである7、また、このアルクリ系合成樹脂の添加は、
得られる塩化ビニル系合成樹脂製タイルの保形性を向上
させる作用も有しており、得られる成形体の物性改良剤
としても作用する、。
(6) Acrylic synthetic resin as a processability improver for vinyl chloride resins Commercially available acrylic resins can be used as they are as processability improvers for vinyl chloride resins3.
, in combination with the aforementioned rock wool or wollastonite with a fiber length of 7 ooμ or less, by Migi/Nogrol/-
This process imparts the required strength to the kneaded material in the toning process, and the gelation of the vinyl chloride synthetic resin is achieved by adding acrylic synthetic resin, which is a processability improver for the vinyl chloride synthetic resin. is accelerated, and a bonding effect with the carbonic acid, which is added as an additive, is expressed7.Additionally, the addition of this alkali-based synthetic resin
It also has the effect of improving the shape retention of the vinyl chloride-based synthetic resin tiles obtained, and also acts as a physical property improver of the obtained molded product.

塩化ビニル系合成樹脂の加工性改良剤たるアクリル系合
成樹脂が、塩化ビニル系重合体700重量部に対してグ
重量部未満では前述の効果が1−分ではなく、また、7
0重量部を越えると添加量の増加の割合にはその効果の
向上がなく不経済となるので、塩化ビニル系重合体の9
〜70重量%の範囲内で添加される。。
If the acrylic synthetic resin, which is a processability improver for vinyl chloride synthetic resin, is less than 700 parts by weight of the vinyl chloride polymer, the above-mentioned effect will not be 1 minute, and
If the amount exceeds 0 parts by weight, the effect will not be improved and the ratio of increase in the amount added will become uneconomical.
It is added within the range of 70% by weight. .

・)1 以下、本発明の塩化ビニル系合成樹脂製タイルの製造方
法の具体的な構成を実施例を以って説明し、併せ、得ら
れた合成樹脂製タイルの物性測定結果を小t。
・)1 Hereinafter, the specific structure of the method for producing a vinyl chloride-based synthetic resin tile of the present invention will be explained with reference to Examples, and the results of measuring the physical properties of the obtained synthetic resin tile will be described below.

実施例/〜q 後記第1表における実施例/〜q欄に示される配合組成
物をハフバリーミキサーにて2分間良く混練し、摩擦熱
により/乙θ〜/ 70 ’Oに熱せら71だ混練物を
得だ3. 4HIらねた混線物をミキン/グロールで/θS〜/ 
35.。Cでノート化し、次いでカレンダーロールに掛
け、厚さ、2mmの長尺状の塩化ビニル果合。
Example/~q The blended composition shown in the Example/~q column in Table 1 below was well kneaded for 2 minutes in a Hufbury mixer, and heated to /O~/70'O by frictional heat. Obtain the kneaded material3. 4HI's mixed wires are mixed with Mikin/Groll/θS~/
35. . C, and then put it on a calendar roll to form a long vinyl chloride sheet with a thickness of 2 mm.

成樹脂製タイル弘+ 、 (b+ 、 (C1、+D+
を成形した。
Plastic tile Hiro+, (b+, (C1, +D+)
was molded.

比較例/ 後記第1人における比較例/欄に示される配合ポIf 
b’Z物を、前+iL”k流側と全く同様に操作し、1
7さ2mmの長尺状5つ塩化ビニル系合成樹脂製タイi
t (Ic)を比較のだめに得た。
Comparative example / Comparison example for the first person listed below / Comparison point If shown in the column
b'Z object is operated in exactly the same way as the previous +iL''k flow side, and 1
7 long 2mm long 5-piece ties made of vinyl chloride synthetic resin
t (Ic) was obtained for comparison.

比較例、!〜3 後記第1表に、L・ける比較例2〜3欄に示される配合
組1j7物を、1)IS記実施例と全く同様に操作した
ところ、カレンダーロールによる圧延工程での塩化ビニ
ル系合成樹脂製ノートの性状が脆く、シートの保形性が
極端に悪いため、タイル状の成形体の素材となるシート
状物に成形することができなかった。
Comparative example! ~3 In Table 1 below, when the formulations 1j7 shown in columns 2 and 3 of Comparative Examples 2 and 3 were operated in exactly the same manner as in 1) IS Example, vinyl chloride-based Because the synthetic resin notebook is brittle and has extremely poor shape retention, it has not been possible to form it into a sheet that can be used as a material for tile-shaped molded objects.

実験 前記実施例/〜グ及び比較例で得られた長尺状の塩化ビ
ニル系合成樹脂製タイル(、A)〜(D)、及び(E)
を、それぞれ縦30夕1g胴、横30ダ1g胴に切断し
、得られた各々の合成樹脂製タイルを、:rxs A 
−3705(ビニル床タイル)に準じて試験した結果の
品質特性を第20表に示す。
Experiment Long vinyl chloride synthetic resin tiles obtained in the above Examples/- and Comparative Examples (A) to (D), and (E)
were cut into 30mm lengthwise 1g pieces and widthwise 30days 1g pieces, and each of the resulting synthetic resin tiles was: rxs A
-3705 (vinyl floor tile) The quality characteristics of the results of the test are shown in Table 20.

以上実施例/〜qにおいては、いずれもカレンダーロー
ルによる圧延工程での塩化ビニル系合成樹脂製シートの
シート保形性が良好であり、従来の、石綿を補強材とし
て使用した比較例/における成形工程での塩化ビニル系
合成樹脂製シートの加工性と略同様の圧延加工性能を有
していた。
In all of the above examples/~q, the sheet shape retention of the vinyl chloride synthetic resin sheet during the rolling process with calendar rolls was good, and the molding in the conventional comparative example/using asbestos as a reinforcing material was found. It had almost the same rolling performance as that of a vinyl chloride synthetic resin sheet in the process.

また、実施例/〜ダにおいて得られた塩化ビニル系合成
樹脂製タイル体)〜(DJの性状は、従来の、石綿を補
強材として使用した比較例/で得られた塩化ビニル系合
成樹脂製タイル(E)の性状と比較して何ら遜色のない
ものであることが、前記実験によって明らかである。
In addition, the properties of DJ (vinyl chloride synthetic resin tile body obtained in Example/~ da)~ (DJ) are as follows: It is clear from the above experiment that the properties are comparable to those of tile (E).

さらに、前記実施例においては、いずれも塩化ビニル系
合成樹脂として、塩化ビニル−酢酸ビニル共重合体を使
用しているが、塩化ビニル系合成樹脂として塩化ビニル
重合体、エチレン−塩化ビニル共重合体あるいはこれら
の混合物を使用する場合においても、成形工程での加工
特性は良好でありt得られる合成樹脂製タイルの性状も
、前記比較例/で得られた塩化ビニル系合成樹脂製タイ
ル(E)と比べ、何ら遜色の無いものであることが確認
されている。
Furthermore, in the above examples, vinyl chloride-vinyl acetate copolymer is used as the vinyl chloride-based synthetic resin, but vinyl chloride polymer, ethylene-vinyl chloride copolymer and ethylene-vinyl chloride copolymer are used as the vinyl chloride-based synthetic resin. Alternatively, even when a mixture of these is used, the processing characteristics in the molding process are good, and the properties of the resulting synthetic resin tile are similar to that of the vinyl chloride synthetic resin tile (E) obtained in the comparative example. It has been confirmed that there is no inferiority in comparison.

本発明の塩化ビニル系合成樹脂製タイルの製造方法は以
上の通りの構成から成るもので、従来の、カレンダーロ
ール方式による塩化ビニル系合成樹脂製タイルの製造に
おいて必須不可欠な成分とされていた石綿を使用するこ
となく、従来の、石綿を使用したカレンダーロール方式
で得られた塩化ビニル系合成樹脂製タイルの性状と比較
して側ら遜色のない塩化ビニル系合成樹脂製タイルを、
カレンダーロール方式にて得るもので、公害防止面に、
字だ操業者の健康管理面に、石綿の使用に伴う悪影響を
何ら発生させることなく、塩化ビニル系合成樹脂製のタ
イルを高度の生産効率で得ることが出来るという作用・
、効果を奏するものである。
The method for producing vinyl chloride synthetic resin tiles of the present invention has the above-mentioned structure. We have created vinyl chloride synthetic resin tiles that are comparable in quality to the vinyl chloride synthetic resin tiles obtained by the conventional calender roll method using asbestos, without the use of asbestos.
Obtained using the calender roll method, it is effective in preventing pollution.
The effect is that tiles made of vinyl chloride-based synthetic resin can be obtained with high production efficiency without causing any adverse effects associated with the use of asbestos in terms of health management for operators.
, it is effective.

特許出願人 日東紡績株式会社 代理人 市  川  理  吉 (外7名)patent applicant Nitto Boseki Co., Ltd. agent Ichi Kawa Riyoshi (7 other people)

Claims (1)

【特許請求の範囲】[Claims] 塩化ビニル重合体、塩化ビニールー酢酸ゼニル共−F合
体、またはエチレン−塩化ビニル共重合体の中から選択
される7種以上の合成樹脂100’R−ivt部と、μ
■塑剤グθ〜55重量部と、安定剤3〜7 「R置部よ
、ロジン変性樹脂または石油変性樹脂/に〜25市量部
と、炭酸カルノウムク00〜フθ0屯椴部と、繊維長7
00μ以下のロックウールまたはウオラストナイト11
0〜/30tM、fitr、部と、塩化ビニル系合成樹
脂の加工性改良剤たるアクリル系合成樹脂グ〜/θ型動
部との混合成分からなる混線物をミキシングロールで7
−ト化し、次いでカレンダーロールで所定の厚さに仕1
−けることを特徴とする合成樹脂製タイルの製造方法。
100'R-ivt portion of seven or more synthetic resins selected from vinyl chloride polymer, vinyl chloride-zenyl acetate co-F polymer, or ethylene-vinyl chloride copolymer, and μ
- 55 parts by weight of plasticizer, 3 to 7 parts by weight of stabilizer, 25 parts by weight of rosin-modified resin or petroleum-modified resin, 00 to 50 parts of carbonate, 3 to 7 parts by weight of stabilizer, long 7
Rock wool or wollastonite 11 below 00μ
A mixed substance consisting of a mixed component of 0~/30tM, fitr, part and an acrylic synthetic resin group~/θ type moving part, which is a processability improver for vinyl chloride synthetic resin, was mixed with a mixing roll.
- It is made into a sheet and then trimmed to a predetermined thickness using a calender roll.
- A method for producing a synthetic resin tile characterized by the ability to
JP9037682A 1982-05-27 1982-05-27 Manufacture of tile made of synthetic resin Granted JPS58208016A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9037682A JPS58208016A (en) 1982-05-27 1982-05-27 Manufacture of tile made of synthetic resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9037682A JPS58208016A (en) 1982-05-27 1982-05-27 Manufacture of tile made of synthetic resin

Publications (2)

Publication Number Publication Date
JPS58208016A true JPS58208016A (en) 1983-12-03
JPS6234342B2 JPS6234342B2 (en) 1987-07-27

Family

ID=13996842

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9037682A Granted JPS58208016A (en) 1982-05-27 1982-05-27 Manufacture of tile made of synthetic resin

Country Status (1)

Country Link
JP (1) JPS58208016A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61190547A (en) * 1984-09-22 1986-08-25 ウオ−ドル・ストレイズ・ピ−エルシ− Manufacture of vibration-controlling and sound-insulating high polymer material formed body
KR100452276B1 (en) * 1997-12-26 2005-06-21 고려화학 주식회사 Vinyl flooring with rosin

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61190547A (en) * 1984-09-22 1986-08-25 ウオ−ドル・ストレイズ・ピ−エルシ− Manufacture of vibration-controlling and sound-insulating high polymer material formed body
JPH0535053B2 (en) * 1984-09-22 1993-05-25 Uoodoru Sutoreizu Plc
KR100452276B1 (en) * 1997-12-26 2005-06-21 고려화학 주식회사 Vinyl flooring with rosin

Also Published As

Publication number Publication date
JPS6234342B2 (en) 1987-07-27

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