JPH033574B2 - - Google Patents
Info
- Publication number
- JPH033574B2 JPH033574B2 JP58023541A JP2354183A JPH033574B2 JP H033574 B2 JPH033574 B2 JP H033574B2 JP 58023541 A JP58023541 A JP 58023541A JP 2354183 A JP2354183 A JP 2354183A JP H033574 B2 JPH033574 B2 JP H033574B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- foam
- sheets
- bismuth
- resin
- 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
- 239000006260 foam Substances 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 8
- 239000004088 foaming agent Substances 0.000 claims description 7
- 229910052797 bismuth Inorganic materials 0.000 claims description 6
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 claims description 5
- 229910000003 Lead carbonate Inorganic materials 0.000 claims description 5
- 229920003051 synthetic elastomer Polymers 0.000 claims description 5
- 239000005061 synthetic rubber Substances 0.000 claims description 3
- UWRBYRMOUPAKLM-UHFFFAOYSA-L lead arsenate Chemical compound [Pb+2].O[As]([O-])([O-])=O UWRBYRMOUPAKLM-UHFFFAOYSA-L 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 239000000057 synthetic resin Substances 0.000 claims description 2
- 238000004898 kneading Methods 0.000 claims 2
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000005060 rubber Substances 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 7
- 239000002932 luster Substances 0.000 description 7
- 239000011049 pearl Substances 0.000 description 6
- 239000004744 fabric Substances 0.000 description 5
- -1 (bismuth) lead carbonate Chemical compound 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- GMZOPRQQINFLPQ-UHFFFAOYSA-H dibismuth;tricarbonate Chemical compound [Bi+3].[Bi+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O GMZOPRQQINFLPQ-UHFFFAOYSA-H 0.000 description 2
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000003760 hair shine Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/002—Methods
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/02—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
- B29C44/10—Applying counter-pressure during expanding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING 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
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/25—Solid
- B29K2105/253—Preform
- B29K2105/256—Sheets, plates, blanks or films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2009/00—Layered products
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Laminated Bodies (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明は発泡体に好輝度(真珠光沢)のメタリ
ツクカラーを出現させる方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a bright (pearlescent) metallic color on a foam.
周知の如く、模造真珠や、熱可塑性樹脂の射出
成形品、或は塩化ビニルレザー化粧品、室内装飾
品、塗装品等においてメタリツクカラーを出現せ
しめたものは存在する発泡体内おいては、メタリ
ツクカラーを現出せしめることは不可能とされ断
念されていたその原因はビスマスの破壊、凝集に
よる輝度の滅殺、及び表面の粗さ等があげられ、
此れらの要因が発泡体にメタリツク光沢を期待す
ることは不可能であると考えられ研究開発が阻ま
れていた。 As is well known, metallic colors appear in imitation pearls, thermoplastic resin injection molded products, vinyl chloride leather cosmetics, interior decoration products, painted products, etc. Metallic colors do not appear in foam products. The causes of this, which had been abandoned as it was considered impossible to make it appear, were the destruction of bismuth, the loss of brightness due to agglomeration, and the roughness of the surface.
Because of these factors, it was considered impossible to expect metallic luster from the foam, and research and development was hindered.
本発明は斯かる問題点を解決し、合成真珠箔で
あるビスマスを破壊凝集から守り、表面阻さを克
服し、見事な発泡体表面に好輝度のメタリツク光
沢を表現せしめることを可能ならしめた発明であ
る。 The present invention solves these problems, protects bismuth, which is a synthetic pearl foil, from destruction and agglomeration, overcomes surface obstruction, and makes it possible to express bright metallic luster on the surface of a splendid foam. It is an invention.
以下、本発明に就いて述べると本発明は、発泡
体の基材としては熱可塑性樹脂と別にゴム材を使
用し、それぞれに発泡剤を含んではいるが未発泡
の材料を作成し、それをシート状に成形した後、
熱可塑性樹脂材のシートの場合は10数枚を積重ね
縦横の長さを500m/m×700m/mの大きさを有
する型窩金型内に入れ、此の金型を150Kg/cm2の
圧力で押圧し、170℃にて20分間加熱し、除圧と
同時に架橋と発泡を行い、シートが一体に融着さ
れた発泡体を得た、(10数枚のシートを積重ねた
理由は、熱の伝導率を有効にする為である)
上記、本発明の実施により出来上つた発泡体は
全面にわたつてあたかも特殊な塗装を施したよう
に輝きメタリツク光沢の好輝度(真珠光沢)を鮮
明に現出せしめ美麗な満足すべき成品を得た。 In the following, the present invention uses a rubber material in addition to a thermoplastic resin as the base material of the foam, creates unfoamed materials that each contain a foaming agent, and then After forming into a sheet,
In the case of sheets of thermoplastic resin, 10 or more sheets are stacked and placed in a cavity mold with dimensions of 500 m/m x 700 m/m, and the mold is heated to a pressure of 150 kg/ cm2. The sheets were pressed together and heated at 170°C for 20 minutes, and at the same time the pressure was removed, crosslinking and foaming were performed to obtain a foam in which the sheets were fused together. (This is to make the conductivity effective.) The foam produced by implementing the present invention shines all over the entire surface as if it were coated with a special coating, and has a clear metallic luster (pearl luster). A beautiful and satisfying product was obtained.
以下、更に本発明を詳述すると、本発明の実施
例に利用する熱可塑性樹脂及びゴムを用いた上述
の場合の樹脂はあくまで一例であつて、塩化ビニ
ル系樹脂、オレフイン系樹脂であつてもよく、
又、オレフイン系樹脂の中では酢酸ビニール、エ
チレンの共重合体が最も好結果が得られることを
確認した。次に、これらの樹脂にはどの樹脂を用
いるにしても発泡剤を含ませて発泡性を与える。
発泡剤は樹脂の軟化点以上の温度において分割
し、ガスを発生するタイプのものが好適でオレフ
イン系樹脂を材料とする場合には発泡剤の他に架
橋剤を添加する。酢酸ビニルエチレンの共重合体
を材料として用いた場合は発泡剤は主にアゾヂカ
ルボンアミド、次にはジニトロソペンタメチレン
テトラミンのような化合物を利用することが望ま
しい。 Hereinafter, to further explain the present invention in detail, the resin in the above-mentioned case using the thermoplastic resin and rubber used in the examples of the present invention is just an example, and even if it is a vinyl chloride resin or an olefin resin. often,
Furthermore, it was confirmed that among the olefin resins, a copolymer of vinyl acetate and ethylene gave the best results. Next, whichever resin is used, a foaming agent is added to impart foamability to the resin.
The foaming agent is preferably one that splits at a temperature higher than the softening point of the resin and generates gas, and when an olefin resin is used as the material, a crosslinking agent is added in addition to the foaming agent. When a copolymer of vinyl acetate ethylene is used as the material, it is preferable to use a compound such as azodicarbonamide as the blowing agent, followed by dinitrosopentamethylenetetramine.
また、架橋剤はジクミルパーオキサイドのよう
な過酸化物を用いる。更に、樹脂には顔料、染
料、充填剤を混入し、その上にビスマス又は炭酸
鉛か或は砒酸鉛を混入し、その混合物を加熱ロー
ルを用いて混練し、ビスマスの結晶を破壊しない
よう又、凝集させないように適正なロール温度
(90°以下)に保持しつゝ未発泡組成物の前記シー
トを成形する。 Further, a peroxide such as dicumyl peroxide is used as a crosslinking agent. Furthermore, pigments, dyes, and fillers are mixed into the resin, and then bismuth, lead carbonate, or lead arsenate is mixed therein, and the mixture is kneaded using heated rolls, taking care not to destroy the bismuth crystals. Then, the sheet of unfoamed composition is molded while maintaining a proper roll temperature (below 90°) to prevent agglomeration.
次に、実施例を挙げ本発明を更に詳述する。 Next, the present invention will be explained in further detail with reference to Examples.
(実施例中の部は重量部を表わす。)
実施例 1
樹脂:酢酸ビニルエチレンの共重合体で酢酸ビニ
ルの共重合体割合15重量%のもの(東洋曹達工
業社製、商標ウルトラセン#630)
発泡剤:(英和化成社製、商標ビニホールAK−
2)
架橋剤:(化薬ヌーリー社製、商標カヤクミルD)
上記樹脂100部に発泡剤6部架橋剤1.4部、ステ
アリン酸1部、炭酸マグネシユーム3部、合成ゴ
ム(日本合成ゴム社製、商標JSR1502)20部、着
色用顔料1.6部(ビスマス)炭酸鉛5.2〜6.5部、こ
れらの混合物を90℃に加熱したミキシングロール
で25分間混練し厚さ0.4m/mのシートに成形す
る。此の場合、此のシートの厚みはかならずしも
0.4m/mに限定されるものではないが、厚みは
0.1m/m〜3m/m迄の範囲が発泡体の仕上り
状態に支障を来たさない範囲であることを確認し
た。此のシートを巾500m/m長さ700m/mの大
きさに裁断し、予め170℃に加熱してあるプレス
内の型窩金型に入れ150Kg/cm2の圧力で押加圧し
20分間経過後除圧と同時に架橋と発泡を行い、シ
ートの一体融着した発泡体を得た。此の実施例1
の方法で得た発泡体は全体的に(ビスマス)炭酸
鉛の適正配向の結果、入射光線を規則的に浮け多
重反射を起こして輝き、剥離、変色の懸念の全く
ない強靭なメタリツクカラーの好輝度(真珠光
沢)を出現しているものが得られた。(The parts in the examples represent parts by weight.) Example 1 Resin: A vinyl acetate ethylene copolymer with a vinyl acetate copolymer content of 15% by weight (manufactured by Toyo Soda Kogyo Co., Ltd., trademark Ultracene #630) ) Foaming agent: (manufactured by Eiwa Kasei Co., Ltd., trademark Vinyhole AK-
2) Crosslinking agent: (manufactured by Kayaku Nouri Co., Ltd., trademark Kayakumil D) 100 parts of the above resin, 6 parts of blowing agent, 1.4 parts of crosslinking agent, 1 part of stearic acid, 3 parts of magnesium carbonate, synthetic rubber (manufactured by Japan Synthetic Rubber Co., Ltd., trademark) JSR1502) 20 parts, coloring pigment 1.6 parts (bismuth), lead carbonate 5.2 to 6.5 parts, these mixtures were kneaded for 25 minutes using a mixing roll heated to 90°C and formed into a sheet with a thickness of 0.4 m/m. In this case, the thickness of this sheet is not necessarily
Although not limited to 0.4m/m, the thickness is
It was confirmed that the range from 0.1 m/m to 3 m/m does not affect the finished state of the foam. This sheet was cut into pieces with a width of 500 m/m and a length of 700 m/m, and was placed in a cavity mold in a press that had been preheated to 170°C and pressed at a pressure of 150 kg/ cm2 .
After 20 minutes, the pressure was removed and at the same time crosslinking and foaming were performed to obtain a foamed sheet with integrally fused sheets. Example 1 of this
As a result of the proper orientation of (bismuth) lead carbonate, the foam obtained by this method regularly reflects the incident light and causes multiple reflections, resulting in a strong metallic color with no concerns of shine, peeling, or discoloration. A product with brightness (pearl luster) was obtained.
実施例 2
発泡体がゴム材料を主材とする場合は前記樹脂
と若干異なり下記の如き製法処方とする。Example 2 When the foam is mainly made of a rubber material, the manufacturing method is slightly different from that of the resin described above, and the manufacturing method is as follows.
ゴム材料
(日本合成ゴム社製 商標 1R2000) 20部
( 〃 商標 BR−01) 25部
(旭化成社製 商標 ソルプレン303) 40部
( 〃 商標 タフデン2000) 15部
以上100部を主原料とし、
発泡剤
TSH(パラトルエンスル アセトン ヒドラゾー
ン)(三協化成社製、商標セルマイク−K)6部
ステアリン 1部
カーボン(日本シリカ社製、商標VN−3ホワイ
トカーボン) 5部
ジ エチレン グリコール 0.5部
加硫速進剤(三新化学社製、商標D、M 1.2部
〃 (三新化学社製、〃 M 0.3部
超加硫速進剤(三新化学社製、〃 T、S 0.2部
硫 黄 1.7部
透明亜鉛華 0.5部
着色用顔料 1.5部
(ビスマス)炭酸鉛 5.5部
以上の配合物を混入、混練するのであるが、ま
ず、第1工程としてゴム部分をロールに巻付け、
ゴムの混練を充分に行ない炭酸鉛のみを残し、他
の薬品全部をロールに巻付け充分に混練が完了し
ている前記ゴムの中へ混入、再び充分に混練を行
なう。此の場合時間は25分、その間ロールの温度
は75℃以下に保ち続ける。Rubber material (manufactured by Japan Synthetic Rubber Co., Ltd., trademark 1R2000) 20 parts (〃 trademark BR-01) 25 parts (manufactured by Asahi Kasei Co., Ltd. trademark Solprene 303) 40 parts (〃 trademark Tuffden 2000) 15 parts The above 100 parts are the main raw materials, and the foaming agent TSH (Paratoluene Sulfur Acetone Hydrazone) (manufactured by Sankyo Kasei Co., Ltd., trademark Cellmic-K) 6 parts Stearin 1 part Carbon (manufactured by Nippon Silica Co., Ltd., trademark VN-3 White Carbon) 5 parts Diethylene Glycol 0.5 parts Vulcanization speed Vulcanization accelerator (manufactured by Sanshin Chemical Co., Ltd., trademark D, M 1.2 parts (manufactured by Sanshin Chemical Co., Ltd., 〃 M 0.3 parts) Super vulcanization accelerator (manufactured by Sanshin Chemical Co., Ltd., 〃 T, S 0.2 parts Sulfur 1.7 parts Transparent zinc white 0.5 parts Coloring pigment 1.5 parts (bismuth) Lead carbonate 5.5 parts The above ingredients are mixed and kneaded, but the first step is to wrap the rubber part around a roll,
The rubber is thoroughly kneaded, leaving only the lead carbonate, and all other chemicals are wound around a roll and mixed into the already thoroughly kneaded rubber, and thoroughly kneaded again. In this case, the time is 25 minutes, during which time the temperature of the roll is kept below 75°C.
練上つたゴム生地は厚みを8m/m〜10m/m
位にして適宜に切出し、約12時間熟成を行なう。 The thickness of the kneaded rubber fabric is 8m/m to 10m/m.
Cut into pieces and ripen for about 12 hours.
此の場合の熟成はスコーチや発泡むらを予防し
安定したものを得る為である。次に熟成の完了し
た生地を1/2当量に2分し、分離した一方の生地
にまだ混入していない炭酸鉛を混入し再び混練を
行ないその結晶を破壊しないよう、又、凝集させ
ないように適正なロール温度(75℃以下が望まし
い)を保持しながら未発泡組成物のシートを成形
し、厚みは2m/mにセツトした、前述の2分し
たもう一方の生地はやはり同じようにロールの温
度を適正に(75℃以下が望ましい)保持しながら
練り上げ厚みを8m/mのシートに成形した、そ
の8m/mのシートの両面にあらかじめ2m/m
のシートに仕上げていた前記(ビスマス)炭酸鉛
混入済の生地を貼付し、その断面は、中心部は普
通の生地をセツトしその両面に(ビスマス)炭酸
鉛入のシートを重接して3層とし、此の3層に重
接した生地を巾500m/m×長さ700m/mの大き
さに裁断し、予め150℃に加熱したプレス内の型
窩金型に入れ150Kg/cm2の圧力で押加圧し15分経
過後除圧と同時に加硫と発泡を行ない重接した生
地が一体に融着した発泡体を得た。その発泡体の
両面は、(ビスマス炭酸鉛の適正配向の結果入射
光線を規則的に受け多重反射を起こして輝き剥
離、変色の懸念の全くない強靭なメタリツクカラ
ーの好輝度(真珠光沢)を鮮明に出現せしめてい
た。故に本発明を実施すると、合成樹脂又はゴム
を主材とした発泡体の表面に従来より不可能とさ
れていたメタリツクカラーの好照度(真珠光沢)
を鮮明に出現せしめることが可能となり、しかも
剥離、変色の懸念が全く無く、履物等に本発明を
利用すると、華麗な揮きを何時迄も維持し得る履
物等が得られる効果を有する発明である。 The purpose of aging in this case is to prevent scorch and uneven foaming and to obtain a stable product. Next, divide the matured dough into 1/2 equivalent parts, mix the lead carbonate that has not yet been mixed into one of the separated dough, and knead it again to avoid destroying the crystals and preventing them from agglomerating. A sheet of unfoamed composition was formed while maintaining an appropriate roll temperature (preferably below 75°C), and the thickness was set at 2 m/m. The other half of the dough was rolled in the same way. While maintaining the temperature appropriately (preferably below 75°C), knead it and form it into a sheet with a thickness of 8 m/m.
The fabric mixed with lead (bismuth) carbonate, which had been finished, was pasted onto the sheet, and its cross section was made up of three layers: a normal fabric was set in the center, and sheets containing lead (bismuth) carbonate were superimposed on both sides. Then, the three-layered fabric was cut into pieces with a width of 500 m/m and a length of 700 m/m, and placed in a mold cavity in a press preheated to 150°C under a pressure of 150 kg/ cm2. After 15 minutes of pressurization, the pressure was removed and at the same time vulcanization and foaming were performed to obtain a foam in which the overlapped fabrics were fused together. Both sides of the foam (as a result of the proper orientation of bismuth lead carbonate) receive incident light regularly and cause multiple reflections, giving it a bright, strong metallic color (pearl luster) with no concerns of peeling or discoloration. Therefore, by carrying out the present invention, a metallic color with good illuminance (pearl luster), which was previously considered impossible, can be achieved on the surface of a foam mainly made of synthetic resin or rubber.
This invention has the effect that it is possible to make it appear clearly, and there is no fear of peeling or discoloration, and that when the present invention is applied to footwear, etc., it is possible to obtain footwear, etc. that can maintain its splendid appearance for any length of time. be.
Claims (1)
ビスマス、又は炭酸鉛、或は砒酸鉛とを混合する
混練ロールを75℃〜90℃に加熱し、前記、混練ロ
ールで約25分間混練した後シート状に成形し、該
シートを重接して予め150℃〜170℃に加熱したプ
レスの型窩内に入れ約150Kg/cm2で押圧して各シ
ートを融着せしめ除圧と同時に発泡せしめ、その
発泡体にメタリツクカラーの好輝度を出現させる
ことを特徴とする発泡体に好輝度のメタリツクカ
ラーを出現させる方法。1. A kneading roll for mixing an unfoamed synthetic resin or rubber material containing a foaming agent with bismuth, lead carbonate, or lead arsenate was heated to 75°C to 90°C, and the mixture was kneaded for about 25 minutes with the kneading roll. After that, the sheets are formed into sheets, and the sheets are overlapped and placed in the cavity of a press preheated to 150°C to 170°C and pressed at approximately 150 kg/cm 2 to fuse each sheet and foam at the same time as the pressure is removed. , A method for making a metallic color appear in a foam with good brightness, characterized by causing the foam to show a good brightness in a metallic color.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58023541A JPS59148640A (en) | 1983-02-14 | 1983-02-14 | Method through which metallic color having favorable brightness is made to display on foamed body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58023541A JPS59148640A (en) | 1983-02-14 | 1983-02-14 | Method through which metallic color having favorable brightness is made to display on foamed body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59148640A JPS59148640A (en) | 1984-08-25 |
| JPH033574B2 true JPH033574B2 (en) | 1991-01-18 |
Family
ID=12113322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58023541A Granted JPS59148640A (en) | 1983-02-14 | 1983-02-14 | Method through which metallic color having favorable brightness is made to display on foamed body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59148640A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110524738A (en) * | 2017-10-16 | 2019-12-03 | 卢巧巧 | The production method of modified form fire-retardant master granule |
-
1983
- 1983-02-14 JP JP58023541A patent/JPS59148640A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59148640A (en) | 1984-08-25 |
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