JPH085987B2 - Method for manufacturing puff base material - Google Patents

Method for manufacturing puff base material

Info

Publication number
JPH085987B2
JPH085987B2 JP19908392A JP19908392A JPH085987B2 JP H085987 B2 JPH085987 B2 JP H085987B2 JP 19908392 A JP19908392 A JP 19908392A JP 19908392 A JP19908392 A JP 19908392A JP H085987 B2 JPH085987 B2 JP H085987B2
Authority
JP
Japan
Prior art keywords
base material
puff
latex composition
latex
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP19908392A
Other languages
Japanese (ja)
Other versions
JPH0614811A (en
Inventor
正純 大西
尚樹 鈴木
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.)
Inoac Corp
Original Assignee
Inoac Corp
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 Inoac Corp filed Critical Inoac Corp
Priority to JP19908392A priority Critical patent/JPH085987B2/en
Publication of JPH0614811A publication Critical patent/JPH0614811A/en
Publication of JPH085987B2 publication Critical patent/JPH085987B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、パフ用基材の製造方法
に関し、更に詳しくは、柔軟性、ソフト感、肌あたり等
が良く、使い心地に優れたパフを簡易、且つ、確実に製
造できるパフ用基材の製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a puff base material, more specifically, a puff that is excellent in flexibility, softness, and feel on the skin and is easy to use, can be produced easily and reliably. The present invention relates to a method for producing a puffable base material.

【0002】[0002]

【従来の技術】従来、化粧用塗布具として使用されてい
たパフは、硬さが F 50〜75°、密度が0.15g
/cm3 程度のものがほとんどであった。ところが、現
在では、柔軟性、ソフト感、肌あたり等が良く、使い心
地に優れたパフを消費者が求めている為、硬さが F
0°、密度が0.12g/cm3程度のパフ用基材を製
造することが必要とされている。そして、この様なパフ
用基材を得るためには、その製造過程において、原料と
なるゴムラテックス、加硫剤、界面活性剤等からなるラ
テックス組成物に、多量の空気を混入し攪拌して発泡さ
せることが有効であることが知られている。
2. Description of the Related Art A puff conventionally used as a cosmetic applicator has a hardness of H F 50 to 75 ° and a density of 0.15 g.
Most of them were about / cm 3 . However, at present, the hardness is H F 3 because consumers are demanding puffs that are good in softness, softness, and feel on the skin and are comfortable to use.
It is necessary to produce a base material for puffs at 0 ° and a density of about 0.12 g / cm 3 . In order to obtain such a puff base material, in the manufacturing process, a large amount of air is mixed with a latex composition composed of a rubber latex as a raw material, a vulcanizing agent, a surfactant, and the like, and the mixture is stirred. It is known that foaming is effective.

【0003】[0003]

【発明が解決しようとする課題】しかし、この多量の空
気を用いる製造方法では、得られたパフ用基材に気泡群
(ムラ)ができ、スポンジの中央部の気泡が大きくな
り、所謂「」ができたり、極端な場合には大きな穴が
でき、パフとして用いることができない場合がある。
However, in this manufacturing method using a large amount of air, a group of bubbles (unevenness) is formed in the obtained puffing base material, and the bubbles in the central portion of the sponge become large, which is a so-called " nest ". In some cases, it may not be possible to use it as a puff.

【0004】本発明は、上記問題点を解決するものであ
り、柔軟性、ソフト感、肌あたり等が良く、使い心地に
優れたパフを簡易、且つ、確実に製造できるパフ用基材
の製造方法を提供することを目的とする。
The present invention solves the above-mentioned problems, and is a method for producing a puff base material which can easily and surely produce a puff which is excellent in flexibility, softness, and touch on the skin and which is excellent in usability. The purpose is to provide a method.

【0005】[0005]

【課題を解決するための手段】本発明者らは、使い心地
に優れたパフを簡易、且つ、確実に製造できるパフ用基
材の製造方法について、鋭意研究した結果、ラテックス
組成物中に混入した空気の分散を良好にし、且つ、ラテ
ックス組成物中に生ずる気泡の潰れを無くすことが有効
であるとの知見を得て本発明を完成するに至ったのであ
る。即ち、本発明のパフ用基材の製造方法は、水溶性ゴ
ムラテックスエマルジョンに少なくとも加硫剤、界面活
性剤、増粘剤及びゲル化剤を添加したラテックス組成物
に、空気を混入し攪拌し、発泡させて加熱加硫で所定形
状のパフ用基材を製造する方法であって、上記ラテック
スエマルジョン中の固形分100重量部に対して、上記
界面活性剤を0.35〜0.50重量部、上記増粘剤
(固形分)を0.01〜0.10重量部配合し、該ラテ
ックス組成物のpHを11.7〜12.0に調整し、上
記攪拌速度を160rpm以上とし、上記ラテックス組
成物の発泡倍率を9〜11倍となるように空気混入量を
調整することを特徴とする。
Means for Solving the Problems The inventors of the present invention have earnestly studied a method for producing a base material for a puff, which can easily and reliably produce a puff excellent in a feeling of use, and as a result, mixed it in a latex composition. The present invention has been completed based on the finding that it is effective to improve the dispersion of the air and eliminate the collapse of bubbles generated in the latex composition. That is, the method for producing a base material for puffs of the present invention is to mix air into a latex composition prepared by adding at least a vulcanizing agent, a surfactant, a thickener and a gelling agent to a water-soluble rubber latex emulsion and stirring the mixture. A method for producing a puffing base material having a predetermined shape by foaming and heat vulcanizing, wherein 0.35 to 0.50 parts by weight of the surfactant is added to 100 parts by weight of the solid content in the latex emulsion. Parts, 0.01 to 0.10 parts by weight of the above-mentioned thickener (solid content) are mixed, the pH of the latex composition is adjusted to 11.7 to 12.0, and the stirring speed is 160 rpm or more. It is characterized in that the amount of air mixed is adjusted so that the expansion ratio of the latex composition is 9 to 11 times.

【0006】上記「ゴムラテックス」成分としては、例
えば、NBR(アクリロニトリル−ブタジエンゴム)、
SBR(スチレン−ブタジエンゴム)、クロロプレンゴ
ム、ブチルゴム、ポリブタジエン、ポリイソプレン等の
ラテックスを挙げることができる。尚、これらのうち、
耐候性、耐油性、衛生面(主に、微生物の発生を抑止す
る効果)等に優れるNBRを用いるのが好ましい。上記
の如く、界面活性剤の添加量を0.35重量部未満とす
るのは、上記ラテックス組成物を均一にできない為、混
入する空気が良好な状態で分散しないためである。一
方、それを0.50重量部を越える量だけ添加しても、
それ以上良好な空気の分散状態が得られ難いと共に、細
かく発泡した気泡が界面活性剤を多量に入れると気泡の
表面張力が弱くなるため、泡が互いにつながり大きな泡
が多くなる。尚、大きな泡は、発泡体にザラツキが出て
化粧性が悪い原因となる。尚、この界面活性剤として
は、例えば、オレイン酸カリウム、ドデシル硫酸ナトリ
ム、ドデシルトリメチルアンモニウムクロリド、ポリオ
キシエチレンアルキルエーテル、N−アルキル−N,N
−ジメチルアンモニウムベタイン等を挙げることができ
る。
Examples of the above-mentioned "rubber latex" component include NBR (acrylonitrile-butadiene rubber),
Examples thereof include latexes such as SBR (styrene-butadiene rubber), chloroprene rubber, butyl rubber, polybutadiene and polyisoprene. Of these,
It is preferable to use NBR which is excellent in weather resistance, oil resistance, hygiene (mainly the effect of suppressing the generation of microorganisms) and the like. As described above, the amount of the surfactant added is less than 0.35 parts by weight because the latex composition cannot be made uniform and the mixed air does not disperse in a good state. On the other hand, even if it is added in an amount exceeding 0.50 parts by weight,
Further, it is difficult to obtain a better dispersed state of air, and when finely foamed bubbles contain a large amount of a surfactant, the surface tension of the bubbles becomes weak, so that bubbles are connected to each other and large bubbles increase. In addition, a large bubble causes roughness in the foam and causes poor cosmetic properties. Examples of the surfactant include potassium oleate, sodium dodecyl sulfate, dodecyltrimethylammonium chloride, polyoxyethylene alkyl ether, N-alkyl-N, N.
-Dimethylammonium betaine etc. can be mentioned.

【0007】また、上記の如く、増粘剤の添加量を定め
るのは、増粘剤が0.01重量部未満の場合には増粘作
用が十分ではなく、上記ラテックス組成物中の気泡を安
定な状態にして、潰れない様にすることが困難であり、
1重量部を越える量を添加しても、増粘効果が高いため
空気を入れて攪拌しても均一な細かい泡ができにくいた
めである。尚、この増粘剤としては、例えば、アルギン
酸ソーダ、ポリアクリル酸ソーダ、ポリアクリル酸アン
モニウム、ポリビニルアルコール等を挙げることができ
る。
Further, as described above, the amount of the thickening agent added is determined so that the thickening effect is not sufficient when the amount of the thickening agent is less than 0.01 parts by weight, and the bubbles in the latex composition are eliminated. It is difficult to make it stable and not to collapse.
This is because even if the amount added exceeds 1 part by weight, the thickening effect is high and even if air is added and stirred, it is difficult to form uniform fine bubbles. Examples of the thickener include sodium alginate, sodium polyacrylate, ammonium polyacrylate, polyvinyl alcohol and the like.

【0008】更に、上記の如く、ラテックス組成物のp
Hを11.7〜12.0の範囲に調整するのは、これに
よりラテックス組成物のゲル化が促進されるからであ
る。即ち、ゲル化剤(pH5〜6)をpHの高いアルカ
リラテックスに入れると、分散系のpHが急降下するた
めゲル化効果が大きい(固まり易い)。従って、発泡時
の細かい気泡のままゲル化できる。また、ラテックスp
Hが低いと、ゲル化効果が悪く気泡がゲル化する前に、
上記のように気泡が連なり大きな泡になる。尚、このp
Hの調整方法は、特に問わず、例えば、水酸化カリウ
ム、水酸化ナトリウム等の水溶液を所定量添加する方法
等が挙げられる。尚、このゲル化剤としては、例えば、
ケイフッ化ソーダ、ケイフッ化カリウム等を挙げること
ができる。
Further, as described above, the p of the latex composition is
The reason for adjusting H to the range of 11.7 to 12.0 is that it promotes gelation of the latex composition. That is, when a gelling agent (pH 5 to 6) is added to an alkaline latex having a high pH, the pH of the dispersion system drops sharply, so that the gelling effect is large (it easily hardens). Therefore, it is possible to gelate the fine bubbles as they are at the time of foaming. Also, latex p
When H is low, the gelling effect is poor and before the bubbles gel,
As described above, the bubbles are connected to form a large bubble. In addition, this p
The method of adjusting H is not particularly limited, and examples thereof include a method of adding a predetermined amount of an aqueous solution of potassium hydroxide, sodium hydroxide, or the like. As the gelling agent, for example,
Examples thereof include sodium silicofluoride and potassium silicofluoride.

【0009】また、上記水溶性ゴムラテックスエマルジ
ョンの添加剤には、上記加硫剤、界面活性剤等の他に、
必要に応じて、加硫助剤、加硫促進剤、老化防止剤、軟
化剤(例えばジオクチルフタレート、ジブチルフタレー
ト等のフタル酸エステル)等を加えることができる。更
に、攪拌速度を160rpm以上とするのは、ラテック
ス組成物中に混入した空気の分散を良好にするためであ
る。更に、上記の如く、発泡倍率を定めるのは、9倍未
満の発泡倍率ではパフ用基材が硬くなり過ぎ、11倍を
越える発泡倍率では、かえってラテックス組成物中に混
入した空気の分散が悪くなるからである。
In addition to the above-mentioned vulcanizing agent, surfactant, etc., the additives of the above water-soluble rubber latex emulsion include
If necessary, a vulcanization aid, a vulcanization accelerator, an antiaging agent, a softening agent (for example, a phthalate such as dioctyl phthalate, dibutyl phthalate, etc.) can be added. Further, the stirring speed is set to 160 rpm or more in order to improve the dispersion of air mixed in the latex composition. Further, as described above, the expansion ratio is determined because the puffing base material becomes too hard when the expansion ratio is less than 9 times, and when the expansion ratio exceeds 11 times, the dispersion of the air mixed in the latex composition is rather poor. Because it will be.

【0010】[0010]

【作用】本発明のパフ用基材の製造方法では、ラテック
ス組成物中の界面活性剤の添加量を増やし、また空気の
混入された同組成物の攪拌速度を大きくし、更にラテッ
クス組成物の発泡倍率が所定範囲に制限される。これに
より、ラテックス組成物中に混入した空気の分散が良好
となる。また、所定量の増粘剤をラテックス組成物に添
加し、更にラテックス組成物のpHを調整するので、こ
の組成物の粘度が上がり、且つ、ゲル化速度が速まり、
そのため、細かい泡が大きな泡に成長する前にゲル化す
る。従って、泡のつながり(成長)を抑え細かい泡で保
持したままゲル化でき、この組成物中の気泡が安定し、
潰れるのが防止される。
In the method for producing a puff substrate of the present invention, the amount of the surfactant added to the latex composition is increased, the stirring speed of the composition mixed with air is increased, and the latex composition is further added. The expansion ratio is limited to a predetermined range. Thereby, the dispersion of air mixed in the latex composition becomes good. Moreover, since a predetermined amount of a thickener is added to the latex composition and the pH of the latex composition is further adjusted, the viscosity of this composition is increased, and the gelation rate is increased.
Therefore, the fine bubbles gel before they grow into large bubbles. Therefore, it can be gelled while suppressing the connection (growth) of bubbles with fine bubbles and stabilizing the bubbles in this composition,
It is prevented from collapsing.

【0011】[0011]

【実施例】以下、実施例により本発明を具体的に説明す
る。 (1)試験片の作製 先ず、表1に示す組成を有する試験品No.1〜3に係
わるラテックス組成物を用意した。
EXAMPLES The present invention will be specifically described below with reference to examples. (1) Preparation of test piece First, a test product No. having the composition shown in Table 1 was prepared. The latex composition concerning 1-3 was prepared.

【0012】[0012]

【表1】 [Table 1]

【0013】尚、表1における組成に関する数値は、各
成分を固形分換算した値であり、その単位は「重量部」
である。また、表中の「NBR−531−B」は、アク
リロニトリルブタジエンゴムの高アクリロニトリル品
〔アクリロニトリルの含有量35重量%(以下、「%」
という。)〕の水系エマルジョン(濃度;65%、日本
ゼオン株式会社製)を示す。更に、表中の「NBR 5
31」は、アクリロニトリルブタジエンゴムの中アクリ
ロニトリル品(アクリロニトリルの含有量25%)の水
系エマルジョン(濃度;65%、日本ゼオン株式会社
製)を示す。
The numerical values relating to the composition in Table 1 are the values obtained by converting each component into solid content, and the unit thereof is "part by weight".
Is. Further, "NBR-531-B" in the table means a high acrylonitrile product of acrylonitrile butadiene rubber [content of acrylonitrile 35% by weight (hereinafter, "%"
Say. )] Water-based emulsion (concentration: 65%, manufactured by Nippon Zeon Co., Ltd.). Furthermore, "NBR 5 in the table
“31” represents an aqueous emulsion (concentration: 65%, manufactured by Nippon Zeon Co., Ltd.) of an acrylonitrile product (acrylonitrile content 25%) in acrylonitrile butadiene rubber.

【0014】また、同表の「イオウ」としては、粉末イ
オウ(細井化学株式会社製)を、「促進剤」としては、
メルカプトベンゾチアゾールの亜鉛塩(商品名「ノクセ
ラーMZ」、大内新興化学株式会社製)を、「酸化亜
鉛」としては、白水化学工業株式会社製のものを用い
た。更に、「老化防止剤」としては、2、2−メチレン
−ビス−4−メチル−6−ターシャリーブチルフェノー
ル(商品名「ノクラックNS−6」、大内新興化学株式
会社製)を、「オレイン酸カリウム」としては、オレイ
ン酸カリ石鹸(花王株式会社製)を用いた。また、「ト
リメンベース」は、塩素化ホルムアルデヒドとアンモニ
アの反応生成物(商品名「トリメンベース」、ユニロイ
ヤル株式会社製)を示し、「アルギン酸ソーダ」(試薬
1級)は、3.3%の水溶液を用いた。更に、「ケイフ
ッ化ソーダ」としては、三井東圧化学株式会社製のもの
を用いた。尚、同表中の「※」印を付す値は、本発明範
囲から外れるもの等である。そして、試験品に係わる各
組成物は、上記各組成成分を混合して調整したものであ
る。
Further, as "sulfur" in the table, powdered sulfur (manufactured by Hosoi Chemical Co., Ltd.) is used, and as "accelerator",
A zinc salt of mercaptobenzothiazole (trade name "NOXCELLER MZ", manufactured by Ouchi Shinko Kagaku Co., Ltd.) and "Zinc oxide" manufactured by Shiramizu Chemical Industry Co., Ltd. were used. Further, as the "antiaging agent", 2,2-methylene-bis-4-methyl-6-tert-butylphenol (trade name "Nocrac NS-6", manufactured by Ouchi Shinko Chemical Co., Ltd.) is used as "oleic acid". As “potassium”, potassium oleate soap (manufactured by Kao Corporation) was used. In addition, "Trimen base" indicates a reaction product of chlorinated formaldehyde and ammonia (trade name "Trimen base", manufactured by Uniroyal Co., Ltd.), and "sodium alginate" (reagent first grade) is 3.3%. An aqueous solution was used. Further, as "sodium fluorosilicate", one manufactured by Mitsui Toatsu Chemicals, Inc. was used. The values marked with "*" in the table are out of the scope of the present invention. Each composition related to the test article is prepared by mixing the above-mentioned composition components.

【0015】次いで、試験品No.1及び3の組成物
に、水酸化カリウムの10%水溶液を所定量添加し、p
Hの値を12に調整した。尚、この様なpH調整を行わ
なかった試験品No.2の組成物のpHの値は、11.
5である。そして、各組成物に、空気を混入した後、ケ
ンミックスミキサ(愛工舎製作所株式会社製)により、
表1に示す各ミキシング速度にて攪拌した。次いで、各
組成物を、成形用筒状体(外径;65mmφ、内径;6
0mmφ)に連続的に流し込み、これを連続的に加熱炉
に搬入して、125℃の下、40分間掛け加熱した。こ
れにより、表1に示す発泡倍率を有し、且つ、連続した
棒状の発泡体(試験品No.1〜3)を得た。尚、この
発泡倍率は、各組成物に混入された空気の量により、調
整されている。更に、上記各発泡体を洗浄、乾燥して、
円柱状(57mmφ)のパフ用基材を得た。そして、各
パフ用基材から、厚さ8mmの略円盤状の片を切り出
し、試験品No.1〜3の各試験片を作製した。
Next, the test product No. A predetermined amount of 10% aqueous solution of potassium hydroxide was added to the compositions of 1 and 3, and p
The value of H was adjusted to 12. In addition, the test product No. which did not perform such pH adjustment. The value of pH of the composition of 2 is 11.
It is 5. Then, after mixing air into each composition, a Kenmix mixer (manufactured by Aikosha Seisakusho Co., Ltd.)
The mixing was performed at each mixing speed shown in Table 1. Then, each composition was treated with a molding cylinder (outer diameter: 65 mmφ, inner diameter: 6
0 mmφ), and this was continuously loaded into a heating furnace and heated at 125 ° C. for 40 minutes. As a result, continuous rod-shaped foams (Test Products Nos. 1 to 3) having the expansion ratios shown in Table 1 were obtained. The expansion ratio is adjusted by the amount of air mixed in each composition. Furthermore, the above foams are washed and dried,
A columnar (57 mmφ) base material for puff was obtained. Then, a substantially disk-shaped piece having a thickness of 8 mm was cut out from each puff base material, and the test product No. Each test piece of 1-3 was produced.

【0016】(2)試験片の評価 先ず、各試験片の硬度と密度を調べた。それらの値を、
表1に併記する。尚硬度は、Fタイプ硬度計を用いて測
定した値である。更に、各試験片の外観と肌に触れたと
きの感触を調べると共に、これらを参考にしてパフ用基
材としての適正の評価を行った。これらの結果も表1に
併記する。
(2) Evaluation of test pieces First, the hardness and density of each test piece were examined. Their values
It is also shown in Table 1. The hardness is a value measured using an F type hardness meter. Furthermore, the appearance of each test piece and the feel when touching the skin were examined, and appropriateness was evaluated as a puff base material with reference to these. These results are also shown in Table 1.

【0017】尚、表1中に示した「外観」に関する評価
は、「○」は「外観が良い」を、「△」は「ピンホール
があり、外観がやや劣る」を、「×」は「基材に大きな
ピンホールが多数存在し、外観が悪い」をそれぞれ示
す。また、「感触」に関する評価は、「○」は「肌触り
が良い」を、「△」は「やや柔軟性に欠け、硬く冷たい
感じがする」を、「×」は「剛性で柔軟性がない」をそ
れぞれ示す。更に、「化粧適正」に関する評価は、
「○」は「パフ用基材に適している」を、「△」は「パ
フとしてやや使い勝手が悪い(即ち、肌触りが悪くゴワ
ゴワした剛性があり、化粧材料がスポンジの泡に入り肌
へ塗れず、また泡の剛性が化粧筋として肌に残る)」
を、「×」は「パフ用基材には適していない(即ち、化
粧筋、肌当たりがタワシのように悪い)」をそれぞれ示
す。
In the evaluation of "appearance" shown in Table 1, "○" means "good appearance", "△" means "slightly inferior appearance with pinholes", and "x" means "poor". "The base material has a large number of large pinholes and the appearance is bad". Regarding the evaluation of "feel", "○" means "feels good on the skin", "△" means "a little lacking in flexibility and feels hard and cold", and "x" means "rigid and inflexible". , Respectively. Furthermore, the evaluation regarding "makeup appropriateness" is
“○” means “suitable for puff base material”, and “△” means that it is a little unusable as a puff (that is, it has a bad texture and a stiff rigidity, and the cosmetic material enters the foam of the sponge and is applied to the skin. Moreover, the rigidity of the foam remains on the skin as a makeup line) "
“X” means “not suitable as a base material for puffs (that is, cosmetic muscles and skin contact are bad like scrubbing)”.

【0018】以上の結果より判断すると、従来品(試験
品No.2)は、硬度、密度とも過度の値を示し、外観
にはピンホールがあり、感触も硬く冷たい感じを受け、
化粧適正においてもペンキを塗るようで化粧ボカシ、肌
シワボカシ等の微細なコントロールができない為、パフ
基材としてやや不適正となっていることが判る。また、
ラテックス組成物中に過度の空気を混入し、発泡倍率を
上げ過ぎた試験品No.3では、組成物中の空気の分散
が悪く、泡の成長が起こるため気泡が大きくなり、ま
た、大きなピンホールが無数にできて外観が悪く、剛性
で感触も悪く、更に化粧筋、肌当たりもタワシのように
悪いと共に、硬度にばらつきを生じる。以上より、これ
はパフ用基材には適していない。一方、本発明品(試験
品No.1)は、気泡が細かく柔軟性、ソフト感、肌あ
たり等が良く、使い心地に優れると共に、外観も良い。
Judging from the above results, the conventional product (test product No. 2) shows excessive hardness and density, has a pinhole on the appearance, and feels hard and cold.
It can be seen that even with proper makeup, since it seems that paint is applied, it is not possible to finely control makeup blurring, skin wrinkles, etc., so it is somewhat inappropriate as a puff base material. Also,
Excessive air was mixed into the latex composition to increase the expansion ratio too much. In No. 3, the air in the composition was poorly dispersed, and bubbles were grown, resulting in large bubbles. In addition, numerous large pinholes were formed and the appearance was poor, and rigidity and touch were poor. Also, it is not as bad as a scrubbing brush, and the hardness varies. From the above, this is not suitable as a puff base material. On the other hand, the product of the present invention (Test product No. 1) has fine air bubbles and good flexibility, softness, and skin contact, and is excellent in the feeling of use and has a good appearance.

【0019】尚、本発明においては、前記具体的実施例
に示すものに限られず、目的、用途に応じて本発明の範
囲内で種々変更した実施例とすることができる。即ち、
パフ用基材は、通常、所望形状への切断、打ち抜き、角
部の面取り等を施し、パフに加工されるが、パフ用基材
に何らの加工を施さず、そのままの状態でパフとして用
いられるものであってもよい。また、パフ用基材の形
状、大きさ等は、特に問わず、目的、用途等に応じて種
々選択される。例えば、本実施例では、円柱状のパフ用
基材を作製したが、シート状のパフ用基材等であっても
よい。
The present invention is not limited to the specific examples described above, and various modifications may be made within the scope of the present invention according to the purpose and application. That is,
The puff base material is usually cut into a desired shape, punched, chamfered at the corners, etc. to be processed into a puff. However, the puff base material is not processed at all and used as it is as a puff. It may be one that is available. Further, the shape, size, etc. of the puffing base material are not particularly limited, and are variously selected according to the purpose, application and the like. For example, in this embodiment, a columnar puff base material was produced, but a sheet-like puff base material or the like may be used.

【0020】[0020]

【発明の効果】以上のように、本発明のパフ用基材の製
造方法によれば、現在の消費者のニーズにマッチした、
外観、柔軟性、ソフト感、肌あたり等が良く、使い心地
に優れたパフを簡易、且つ、確実に製造できる。
As described above, according to the method for producing a puff base material of the present invention, it is possible to meet the current needs of consumers.
A puff that has good appearance, flexibility, softness, and skin feel, and is easy to use can be manufactured easily and reliably.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 水溶性ゴムラテックスエマルジョンに少
なくとも加硫剤、界面活性剤、増粘剤及びゲル化剤を添
加したラテックス組成物に、空気を混入し攪拌し、発泡
させて加熱加硫して所定形状のパフ用基材を製造する方
法であって、 上記ラテックスエマルジョン中の固形分100重量部に
対して、上記界面活性剤を0.35〜0.50重量部、
上記増粘剤(固形分)を0.01〜0.10重量部配合
し、該ラテックス組成物のpHを11.7〜12.0に
調整し、 上記攪拌速度を160rpm以上とし、上記ラテックス
組成物の発泡倍率を9〜11倍となるように空気混入量
を調整することを特徴とするパフ用基材の製造方法。
1. A latex composition prepared by adding at least a vulcanizing agent, a surfactant, a thickener and a gelling agent to a water-soluble rubber latex emulsion, agitating, foaming, and heat vulcanizing. A method for producing a puffing base material having a predetermined shape, which comprises adding 0.35 to 0.50 part by weight of the surfactant to 100 parts by weight of the solid content in the latex emulsion.
0.01 to 0.10 parts by weight of the above thickener (solid content) is blended, the pH of the latex composition is adjusted to 11.7 to 12.0, the stirring speed is 160 rpm or more, and the latex composition is A method for producing a base material for a puff, which comprises adjusting the amount of air mixed so that the expansion ratio of the product is 9 to 11.
JP19908392A 1992-07-01 1992-07-01 Method for manufacturing puff base material Expired - Fee Related JPH085987B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19908392A JPH085987B2 (en) 1992-07-01 1992-07-01 Method for manufacturing puff base material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19908392A JPH085987B2 (en) 1992-07-01 1992-07-01 Method for manufacturing puff base material

Publications (2)

Publication Number Publication Date
JPH0614811A JPH0614811A (en) 1994-01-25
JPH085987B2 true JPH085987B2 (en) 1996-01-24

Family

ID=16401822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19908392A Expired - Fee Related JPH085987B2 (en) 1992-07-01 1992-07-01 Method for manufacturing puff base material

Country Status (1)

Country Link
JP (1) JPH085987B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998018860A1 (en) * 1996-10-25 1998-05-07 Nippon Zeon Co., Ltd. Latex of conjugated diene polymer rubber, rubber latex composition, and rubber foam
WO2009145009A1 (en) * 2008-05-30 2009-12-03 日本ゼオン株式会社 Copolymer latex composition for foam rubber, copolymer latex composition for vulcanizable foam rubber, and foam rubber
JP4872016B1 (en) * 2010-10-20 2012-02-08 株式会社イノアック技術研究所 Cosmetic applicator
JP5859693B1 (en) * 2015-03-04 2016-02-10 日本エイアンドエル株式会社 Foam rubber aqueous composition and foam rubber

Also Published As

Publication number Publication date
JPH0614811A (en) 1994-01-25

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