JPH0518987B2 - - Google Patents
Info
- Publication number
- JPH0518987B2 JPH0518987B2 JP58096270A JP9627083A JPH0518987B2 JP H0518987 B2 JPH0518987 B2 JP H0518987B2 JP 58096270 A JP58096270 A JP 58096270A JP 9627083 A JP9627083 A JP 9627083A JP H0518987 B2 JPH0518987 B2 JP H0518987B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- vinyl
- asbestos
- parts
- acid
- 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
Links
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
- 239000010425 asbestos Substances 0.000 claims description 14
- 229910052895 riebeckite Inorganic materials 0.000 claims description 14
- 239000004800 polyvinyl chloride Substances 0.000 claims description 13
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- 229920005989 resin Polymers 0.000 claims description 13
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 9
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 13
- 229920002554 vinyl polymer Polymers 0.000 description 13
- 239000004014 plasticizer Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 239000003610 charcoal Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004709 Chlorinated polyethylene Substances 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- MHVJRKBZMUDEEV-APQLOABGSA-N (+)-Pimaric acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CC[C@](C=C)(C)C=C2CC1 MHVJRKBZMUDEEV-APQLOABGSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N Diethylhexyl phthalate Natural products CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- KGMSWPSAVZAMKR-UHFFFAOYSA-N Me ester-3, 22-Dihydroxy-29-hopanoic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(=C(C)C)C=C1CC2 KGMSWPSAVZAMKR-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- KGMSWPSAVZAMKR-ONCXSQPRSA-N Neoabietic acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CCC(=C(C)C)C=C2CC1 KGMSWPSAVZAMKR-ONCXSQPRSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 ethylene, propylene, vinyl Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- DJDSLBVSSOQSLW-UHFFFAOYSA-N mono(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(O)=O DJDSLBVSSOQSLW-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Description
本発明は優秀なポリ塩化ビニル系のビニルアス
ベスト床タイルの代替品に関する。
従来よりビニルアスベスト床タイルは通常充填
剤がポリ塩化ビニル樹脂100重量部に対して200重
量部以上含有されており、安価で寸法安定性等の
物理的性質を満足させた床材として普及してい
る。しかしながらアスベストは特定化学物質に指
定されているため作業環境の整備を必要とすると
共に、できれば全く使用されないことが望まし
く、アスベスト代替品についての研究が行われて
いる。公知のアスベスト床タイルの代替品として
は、特開昭55−71745号公報に繊維石膏を使用し
たものが提案されているが、繊維石膏は現在、非
常に高価ないしは入手不能である。またガラス繊
維を使用したものもあるが、寸法安定性が悪いと
いう欠点がある。また従来はビニル床タイルの加
工性を高めるために2次可塑剤を添加していた
が、その場合には耐曲げ、耐衝撃性が低下する欠
点があつた。
本発明の目的はアスベストを何ら含まずとも、
ビニルアスベスト床タイルと同等の性能を有する
ビニル床タイルを提供することにある。
また本発明の目的は入手容易であり、比較的安
価な充填剤を使用したビニル床タイルを提供する
ことにある。
更に本発明の目的は2次可塑剤を全く使用しな
くてもよいビニル床タイルを提供することにあ
る。
本発明はポリ塩化ビニル系床タイルにおいて、
充填剤として、アスベストを含まず、樹脂酸で処
理された炭酸カルシウムをポリ塩化ビニル樹脂
100重量部に対して4〜440重量部含有したことを
特徴とするビニル床タイルに係る。
本発明に使用するポリ塩化ビニル樹脂(PVC)
は塩化ビニルのホモポリマーでも良く、また塩化
ビニルとエチレン、プロピレン、酢酸ビニル、ア
クリル酸もしくはメタクリル酸またはこれらのエ
ステル等の他のモノマーとのコポリマーでも良
い。また少量のスチレン・ブタジエンゴム
(SBR)、ニトリル・ブタジエンゴム(NBR)、
塩素化ポリエチレン、アクリロニトリル・ブタジ
エン・スチレン(ABS)樹脂等をブレンドする
こともできる。
本発明で使用される充填剤は樹脂酸で処理され
た炭酸カルシウム(以下「処理炭カル」と略す)
であり、PVC100部(重量部、以下同様)に対し
て4〜440部使用する。上記において樹脂酸とは、
例えばジテルペン酸、アビエチン酸、ネオアビエ
チン酸、d−ピマル酸、安息香酸、桂皮酸等の天
然樹脂中に遊離し、またはエステルもしくは塩と
して存在する樹脂酸、石油樹脂と不飽和カルボン
酸をグラフト結合させて得られた樹脂酸を主成分
としたもの、および所望により、この樹脂酸の
塩、樹脂酸を一部エステル化等したものなどを挙
げることができる。樹脂酸による処理方法として
は例えば炭酸カルシウムの濃縮スラリーを攪拌し
ながら樹脂酸溶液を添加し、次いで過、乾燥、
粉砕する方法を挙げることができる。
上記で用いられる炭酸カルシウムは通常その粒
度が約0.02〜350μ、好ましくは約0.02〜10μ、更
に好ましくは約0.04〜0.2μのものが使用される。
本発明では上記処理炭カルがPVC100部に対し
て4部未満の場合には吸水による寸法変化が大き
くなり、また加工性(主としてロールへのなじ
み)が悪くなる。また440部を越えると混練され
たタイル組成物のロール離れが悪くなり、またタ
イル加工中に気泡が生じてタイル外観が悪くない
望ましくない。また樹脂酸で処理されない充填剤
のみ使用した場合は吸水による寸法安定性、ロー
ルへのタツク等の加工性が悪くなる。本発明では
上記処理炭カル以外に、副次的に他の充填剤を配
合することもできる。このようなものとして例え
ば樹脂酸で処理されない炭酸カルシウム、シリ
カ、タルク、ポリエステル、セルロース等の有機
繊維、その他アスベスト以外の無機繊維等を挙げ
ることができる。本発明における充填剤の総量は
PVC100部に対して200部以上とするのが好まし
い。この場合には特に優れた寸法安定性が得られ
る。
本発明では他の添加剤として従来のPVC系床
材に使用されている1次可塑剤、安定剤、着色剤
等を配合することも任意である。1次可塑剤とし
ては2−エチルヘキシルフタレート、ブチルベン
ジルフタレート等の公知の可塑剤を好適には15〜
55部使用できる。
本発明床タイルの製造方法は前記の如く、
PVCに可塑剤、安定剤、着色剤等と共に前記本
発明の効果を発揮すべく処理炭カルと他の充填剤
を配合した配合組成物を例えばリボンブレンダー
等により混合し、次いでバンバリーミキサー等に
よつて加熱混練し、更に所定温度に保たれたミキ
シングロールで〓練し、続いて所定温度に保持さ
れたカレンダーロールを通過させて所定厚みのシ
ート素材を製造する。ここでミキシングロール、
カレンダーロールの加熱温度は原料の塩化ビニル
系樹脂の種類や原料各成分の配合割合等によつて
適宜定められるものであるが、一般にこの温度は
150〜180℃に間に定められる場合が多い。このシ
ート素材は一定寸法例えば303mm×303mm等に切抜
けばこのままでも床または壁用被覆材料となるも
のである。なお本発明においては樹脂組成物を一
度シートに形成した後、これをペレツト化し再度
カレンダーロールでシート化するについては何ら
差支えない。
本発明のビニル床タイルはアスベスを使用せず
とも処理炭カルを特定量使用することにより、加
工性、へこみ値、加熱による長さ変化量、吸水に
よる寸法変化、反り、曲げ、衝撃による割れ、そ
の他の物性において、従来のビニルアスベストタ
イルと比較して何ら差のないアスベストを全面的
に置換した優れた床タイルであり、しかも低コス
トで有利に製造することができる。また従来、床
タイル成分として必須であつたクマロン−インデ
ン樹脂、石油樹脂、松ヤニ、塩素化ポリエチレン
等の2次可塑剤を全く使用せずとも何ら性能上問
題ないという長所をも有している。
以下に実施例、比較例を挙げて説明する。
実施例1〜5及び比較例1〜3
第1表の配合組成物を180℃のバンバリーミキ
サーにて粗混練し、160℃のミキシングロールで
仕上げ混練し、次いでカレンダーロールで圧延し
て2mm厚のシートを得た。このシートを130℃の
炉中でアニーリングを行い、室温に冷却後、1辺
が303mmの正方形に打抜いて床タイルを得た。得
られた床タイルの諸物性をJIS A 5705及びFS
(Federal Specifications、LF−001641、GSA−
FSS)規格に基づいて測定し、その結果を第2表
に示した。処理炭カルとしては石油樹脂と無水マ
レイン酸を反応させて得られた樹脂酸に、無水フ
タル酸とエチレングリコールを反応させて得られ
た樹脂により処理した平均粒径0.08μの炭酸カル
シウムを使用した。
尚第2表の加工性の評価において、○は優れ
る、△はやや良い、×は劣るを示し、変化量(※)
における単位は10-2mmである。
また曲げは床タイルを円筒に沿わせた場合に、
亀裂の生ずる円筒の最大径で表わしたものであ
る。
The present invention relates to an excellent alternative to polyvinyl chloride-based vinyl asbestos floor tiles. Conventionally, vinyl asbestos floor tiles usually contain 200 parts by weight or more of filler per 100 parts by weight of polyvinyl chloride resin, and have become popular as a flooring material that is inexpensive and satisfies physical properties such as dimensional stability. There is. However, since asbestos is designated as a specified chemical substance, it is necessary to improve the working environment, and if possible, it is desirable to not use it at all, and research is being conducted on asbestos substitutes. As a substitute for the known asbestos floor tiles, one using fiber gypsum has been proposed in Japanese Patent Application Laid-open No. 71745/1982, but fiber gypsum is currently very expensive or unavailable. There are also products that use glass fiber, but they have the disadvantage of poor dimensional stability. In addition, conventionally, secondary plasticizers have been added to improve the workability of vinyl floor tiles, but this has the drawback of decreasing bending resistance and impact resistance. The purpose of the present invention is to provide a system that does not contain asbestos.
To provide a vinyl floor tile having performance equivalent to that of a vinyl asbestos floor tile. It is also an object of the present invention to provide a vinyl floor tile using a filler that is readily available and relatively inexpensive. A further object of the present invention is to provide a vinyl floor tile that does not require the use of any secondary plasticizers. The present invention relates to polyvinyl chloride floor tiles,
As a filler, asbestos-free calcium carbonate treated with resin acid is used in polyvinyl chloride resin.
It relates to a vinyl floor tile characterized by containing 4 to 440 parts by weight per 100 parts by weight. Polyvinyl chloride resin (PVC) used in the present invention
may be a homopolymer of vinyl chloride or a copolymer of vinyl chloride and other monomers such as ethylene, propylene, vinyl acetate, acrylic acid or methacrylic acid or esters thereof. In addition, small amounts of styrene-butadiene rubber (SBR), nitrile-butadiene rubber (NBR),
It is also possible to blend chlorinated polyethylene, acrylonitrile butadiene styrene (ABS) resin, etc. The filler used in the present invention is calcium carbonate treated with resin acid (hereinafter abbreviated as "treated carbonate").
It is used in an amount of 4 to 440 parts per 100 parts (by weight, hereinafter the same) of PVC. In the above, resin acid is
For example, resin acids such as diterpenic acid, abietic acid, neoabietic acid, d-pimaric acid, benzoic acid, cinnamic acid, etc., which are free in natural resins or exist as esters or salts, and petroleum resins are grafted to unsaturated carboxylic acids. Examples include those whose main component is a resin acid obtained by oxidation, and, if desired, salts of this resin acid, and those obtained by partially esterifying the resin acid. As a treatment method using a resin acid, for example, a resin acid solution is added to a concentrated slurry of calcium carbonate while stirring, and then filtered, dried, and
A method of pulverization can be mentioned. The calcium carbonate used above usually has a particle size of about 0.02 to 350 microns, preferably about 0.02 to 10 microns, and more preferably about 0.04 to 0.2 microns. In the present invention, if the amount of the treated carbon is less than 4 parts per 100 parts of PVC, dimensional changes due to water absorption will be large and workability (mainly roll conformability) will be poor. Moreover, if the amount exceeds 440 parts, the kneaded tile composition will not easily separate from the rolls, and bubbles will be generated during tile processing, which is not desirable since the appearance of the tile will be poor. Furthermore, if only a filler that is not treated with a resin acid is used, the dimensional stability due to water absorption and processability such as tackiness on rolls will deteriorate. In the present invention, in addition to the above-mentioned treated charcoal, other fillers may be added as a subsidiary. Examples of such materials include organic fibers such as calcium carbonate, silica, talc, polyester, and cellulose that are not treated with resin acids, and other inorganic fibers other than asbestos. The total amount of filler in the present invention is
It is preferable to use 200 parts or more per 100 parts of PVC. In this case, particularly excellent dimensional stability is obtained. In the present invention, other additives such as primary plasticizers, stabilizers, colorants, etc., which are used in conventional PVC flooring materials, may optionally be added. As the primary plasticizer, a known plasticizer such as 2-ethylhexyl phthalate or butylbenzyl phthalate is preferably used in an amount of 15 to
55 copies available. The method for manufacturing floor tiles of the present invention is as described above.
A blended composition containing PVC, plasticizers, stabilizers, colorants, etc., as well as treated coal and other fillers to exhibit the effects of the present invention is mixed using, for example, a ribbon blender, and then using a Banbury mixer or the like. The mixture is heated and kneaded, further kneaded with a mixing roll kept at a predetermined temperature, and then passed through a calender roll kept at a predetermined temperature to produce a sheet material of a predetermined thickness. Mixing roll here,
The heating temperature of the calender roll is determined appropriately depending on the type of raw material vinyl chloride resin and the blending ratio of each raw material component, but generally this temperature is
It is often set between 150 and 180℃. If this sheet material is cut out to a certain size, such as 303 mm x 303 mm, it can be used as a covering material for floors or walls. In the present invention, there is no problem in forming the resin composition into a sheet, and then pelletizing the resin composition and forming it into a sheet again using a calender roll. The vinyl floor tiles of the present invention do not use asbestos, but by using a specific amount of treated charcoal, they can improve workability, dent value, length change due to heating, dimensional change due to water absorption, warping, bending, cracking due to impact, etc. It is an excellent floor tile that completely replaces asbestos, with no difference in other physical properties compared to conventional vinyl asbestos tiles, and it can be advantageously manufactured at low cost. It also has the advantage of not causing any performance problems even without the use of secondary plasticizers such as coumaron-indene resin, petroleum resin, pine resin, and chlorinated polyethylene, which have conventionally been essential as floor tile components. . Examples and comparative examples will be described below. Examples 1 to 5 and Comparative Examples 1 to 3 The blended compositions shown in Table 1 were roughly kneaded in a Banbury mixer at 180°C, finished kneaded in a mixing roll at 160°C, and then rolled with a calendar roll to form a 2 mm thick sheet. Got a sheet. This sheet was annealed in a furnace at 130°C, cooled to room temperature, and then punched into squares with sides of 303 mm to obtain floor tiles. The physical properties of the obtained floor tiles were determined according to JIS A 5705 and FS.
(Federal Specifications, LF−001641, GSA−
The results are shown in Table 2. As the treated carbon, calcium carbonate with an average particle size of 0.08μ was used, which was treated with a resin obtained by reacting phthalic anhydride and ethylene glycol with a resin acid obtained by reacting petroleum resin and maleic anhydride. . In the evaluation of workability in Table 2, ○ indicates excellent, △ indicates slightly good, × indicates poor, and the amount of change (*)
The unit in is 10 -2 mm. Also, bending occurs when the floor tile is placed along a cylinder.
It is expressed as the maximum diameter of the cylinder where a crack occurs.
【表】【table】
【表】【table】
【表】
表より、実施例1〜5において、ほぼ同一の厚
さと認められる本発明のビニル床タイルが加工性
良く得られ、これらの諸物性は従来のビニルアス
ベストタイルと比較して大差がないことが明らか
である。
実施例1においては処理炭カルが10部程度しか
入つていないにも拘らず良好な物性が得られ、ま
た実施例5においても加工性は損なわれなかつ
た。比較例1は公知のビニルアスベストタイルの
代表的な配合例である。比較例2は処理炭カルを
全く使用しない場合、比較例3は処理炭カルが4
部未満の場合で、いずれの場合も加工性、加熱に
よる長さ変化量、吸水による寸法変化量、反り、
曲げ、衝撃により割れに至るまでの回数等の面で
著しく劣り、特に2次可塑剤を添加することによ
り低温特性が著しく低下した。[Table] From the table, in Examples 1 to 5, the vinyl floor tiles of the present invention with almost the same thickness were obtained with good workability, and these physical properties were not significantly different from those of conventional vinyl asbestos tiles. That is clear. In Example 1, good physical properties were obtained even though only about 10 parts of treated coal was contained, and in Example 5, workability was not impaired either. Comparative Example 1 is a typical formulation example of a known vinyl asbestos tile. Comparative Example 2 uses no treated charcoal, and Comparative Example 3 uses 4 treated charcoal.
In either case, the processability, length change due to heating, dimensional change due to water absorption, warpage,
It was significantly inferior in terms of the number of times it took to crack due to bending and impact, and especially when a secondary plasticizer was added, the low-temperature properties were significantly reduced.
Claims (1)
として、アスベストを含まず、樹脂酸で処理され
た炭酸カルシウムをポリ塩化ビニル樹脂100重量
部に対して4〜440重量部含有したことを特徴と
するビニル床タイル。1. A polyvinyl chloride floor tile, characterized in that it does not contain asbestos and contains 4 to 440 parts by weight of calcium carbonate treated with resin acid based on 100 parts by weight of polyvinyl chloride resin as a filler. floor tiles.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9627083A JPS59220555A (en) | 1983-05-30 | 1983-05-30 | Vinyl floor tile |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9627083A JPS59220555A (en) | 1983-05-30 | 1983-05-30 | Vinyl floor tile |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59220555A JPS59220555A (en) | 1984-12-12 |
JPH0518987B2 true JPH0518987B2 (en) | 1993-03-15 |
Family
ID=14160454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9627083A Granted JPS59220555A (en) | 1983-05-30 | 1983-05-30 | Vinyl floor tile |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59220555A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6134290A (en) * | 1984-07-20 | 1986-02-18 | Maruo Calcium Kk | Polyvinyl vinyl chloride resin tile |
CN103232651A (en) * | 2013-04-27 | 2013-08-07 | 苏州市德莱尔建材科技有限公司 | Polyvinyl chloride (PVC) floor tie and preparation method thereof |
CN104530604A (en) * | 2015-01-03 | 2015-04-22 | 天台县品信地板有限公司 | Formula of novel environment-friendly and flame-retarding macromolecule PVC plastic floor |
TW201708673A (en) * | 2015-07-02 | 2017-03-01 | Afi授權有限責任公司 | Laminated surface coverings |
WO2019206823A1 (en) * | 2018-04-23 | 2019-10-31 | Byk-Chemie Gmbh | Filled polyvinyl chloride composition |
JP7033359B1 (en) * | 2021-09-29 | 2022-03-10 | 株式会社Tbm | Polyvinyl chloride resin sheet for flooring |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5092342A (en) * | 1973-12-20 | 1975-07-23 |
-
1983
- 1983-05-30 JP JP9627083A patent/JPS59220555A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5092342A (en) * | 1973-12-20 | 1975-07-23 |
Also Published As
Publication number | Publication date |
---|---|
JPS59220555A (en) | 1984-12-12 |
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