JPS59109540A - Sbr latex composition - Google Patents
Sbr latex compositionInfo
- Publication number
- JPS59109540A JPS59109540A JP57219242A JP21924282A JPS59109540A JP S59109540 A JPS59109540 A JP S59109540A JP 57219242 A JP57219242 A JP 57219242A JP 21924282 A JP21924282 A JP 21924282A JP S59109540 A JPS59109540 A JP S59109540A
- Authority
- JP
- Japan
- Prior art keywords
- latex
- microballoon
- sbr latex
- inorg
- hollow bodies
- 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.)
- Pending
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はSBRラテックス組成物、符に無機質の微小中
空体を混入したカーペットのバッキング剤に適した組成
物に係るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an SBR latex composition, a composition suitable for use as a carpet backing agent, in which inorganic micro-hollow bodies are mixed.
従来カーペットのバッキング剤としてSBRラテックス
組成物が用いられてきたが、かかる組成中には例えばラ
テックス固形分100部当9350〜450部程度の炭
酸カルシウムの他増粘剤、消泡剤が混入されてきた。Conventionally, SBR latex compositions have been used as backing agents for carpets, but such compositions contain, for example, about 9,350 to 450 parts of calcium carbonate, thickeners, and antifoaming agents per 100 parts of latex solid content. Ta.
しかしながら、かかる従来法においては主として混入さ
れる炭酸カルシウムに基因して比較的重量が重く、又ラ
テックス組成物をカーペットに施こした際、カーペット
を折り曲げるとヒビが生ずる等屈曲性が必ずしも良好で
なく、又最近の近隣騒音問題とも関連のある吸晋性等が
必ずしも満足し得るものではなかった。However, in this conventional method, the weight is relatively heavy mainly due to the calcium carbonate mixed in, and when the latex composition is applied to the carpet, the flexibility is not necessarily good, such as cracks occurring when the carpet is bent. Moreover, the absorbency, which is related to recent neighborhood noise problems, was not necessarily satisfactory.
本発明者は、これらの点に鑑み特に軽量化を有効に行な
える手段につき種々研究、検討した結果、実質的に吸引
性及び浴解性のない無@負の微小中空体を炭酸カルシウ
ムに代えて用いることによシ前記目的を達成し得ること
を見出し、本発明はこれを要旨とするものである。In view of these points, the present inventor has conducted various studies and examinations on effective means for weight reduction, and has determined that calcium carbonate can be replaced with negative micro hollow bodies that have virtually no suction or bath disintegrability. It has been discovered that the above object can be achieved by using the same, and this is the gist of the present invention.
本発明において用いられる無札、質の中空体としては、
例えばシリカ、シリカアルミナ、アルミナ、アルミナ、
ジルコニア等特に限定はない。The unlabeled hollow body used in the present invention includes:
For example, silica, silica alumina, alumina, alumina,
Zirconia etc. are not particularly limited.
又、これら中空体の平均粒径としてはあま9細かすぎる
と中空体なるが故の好ましい性質を期待し得す、逆にあ
まり大きすぎるとラテックス組成物として必要とされる
性質や性能を阻害するので何れも好1しくなく、この為
平均粒径は一般に10〜300μ程度を採用するのが適
当である。In addition, if the average particle size of these hollow bodies is too small, favorable properties can be expected because of the hollow bodies, but on the other hand, if they are too large, the properties and performance required for the latex composition will be inhibited. Therefore, neither is preferable or unfavorable, and for this reason, it is generally appropriate to adopt an average particle size of about 10 to 300 μm.
これら中を体は、実質的に吸水性及び溶解性のないこと
が必要である。その理由は、5BIRラテツクスは一般
に50%程度の水を有してお9、吸水性乃至溶解性であ
るとかかる水が中空体の殻を通して中空部に浸入したわ
、或は殻自体を1彫潤することによシ中空体がつぶれて
@量化等の所期の目的を達成し得ガくなる為である。It is necessary for the body in these materials to be substantially non-absorbent and non-soluble. The reason for this is that 5BIR latex generally has about 50% water9, and if it is water-absorbing or soluble, this water may enter the hollow part through the shell of the hollow body, or the shell itself may be carved. This is because by moistening, the hollow body collapses and achieves the desired purpose such as quantification.
この為、中空体の実質的な吸水性及び溶解性を阻止する
手段としては、一つは中空体が有す殻を高温においてガ
ラス化する手段、一つは中壁体表面に散水処理を施こす
ことである。このうち、撥水処理を施こす手段としては
、例えばγ−メタアクリロキシグロビルトリメトキシシ
ラン、ビニルトリエトキシシラン、γ−アミノプロピル
トリエトキシシラン、N−β(アミノエチル)γニアミ
ノプロピルトリメトキシシラン、β−(3,4エポキシ
シクロヘキシル)エチルトリメトキシシラン2.γ−グ
リシドキシプロビルトリメトキシシラン、γ−メルカプ
トプロピルトリメトキシシラン、N−β(アミノエチル
)γ−アミノプロピルメチルジメトキシシラン、γ−ク
ロロプロピルトリメトキシシラン等のシランカップリン
グ剤や、C8〜18を有するパーフルオロアルキル基含
有化合物7會ひ含弗累系振水剤等を用い、これらを中空
体弄面に被覆せしめるのが適当である。For this reason, there are two ways to prevent substantial water absorption and solubility of the hollow body: one is to vitrify the shell of the hollow body at high temperature, and the other is to spray water on the surface of the inner wall. It's about rubbing. Among these, examples of water-repellent treatment include γ-methacryloxyglobyltrimethoxysilane, vinyltriethoxysilane, γ-aminopropyltriethoxysilane, and N-β(aminoethyl)γ-niaminopropyltrimethoxysilane. Methoxysilane, β-(3,4 epoxycyclohexyl)ethyltrimethoxysilane2. Silane coupling agents such as γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, N-β(aminoethyl)γ-aminopropylmethyldimethoxysilane, γ-chloropropyltrimethoxysilane, and C8 It is appropriate to use a perfluoroalkyl group-containing compound having a perfluoroalkyl group of 7 to 18 and coat the surface of the hollow body with a fluorostatic shaking agent or the like.
更にこれら中空体は、真比重が0.1〜0.3g/α程
度を採用するのが適当である。比重が上記範囲を超える
と軽重化の目的を動床的に達。Furthermore, it is appropriate that these hollow bodies have a true specific gravity of about 0.1 to 0.3 g/α. If the specific gravity exceeds the above range, the purpose of weight reduction will be achieved.
成し難く、逆に前記範囲に満たない場合にはラテックス
狭面に浮き出してくる虞れがあるので何れも好ましくな
い。On the other hand, if it is less than the above range, there is a risk that the latex will stand out on the narrow surface, so both are not preferred.
又、中空体の静水圧中での破壊強度はほぼ20〜100
地程度のものが適当である。かくして、かかる中空体を
SDRラテックス中に混入せしめる量としてはラテック
スの固形分100車量部に対し、10〜50重重部程度
型部用するのが適当である。混入量が前記範囲に満たな
い場合には靴量化、風合い、吸音特性等が充分に発揮で
きず、逆に前記範囲を超える場合にはコンパウンドの強
度が低下し、カーペットの抜糸強度、剥離強度等が低下
する虞れがあるので何れも好ましくない。In addition, the breaking strength of the hollow body under hydrostatic pressure is approximately 20 to 100
Something of the same size as the earth is suitable. Thus, the appropriate amount of such hollow bodies to be mixed into the SDR latex is about 10 to 50 parts by weight per 100 parts by weight of the solid content of the latex. If the amount of the compound is less than the above range, the shoe mass, texture, sound absorption properties, etc. will not be fully exhibited, and if it exceeds the above range, the strength of the compound will decrease, and the strength of the carpet, such as the thread removal strength and peel strength, will be reduced. Both are unfavorable as there is a risk that the
かくして本発明によるSBRラテックス組成″* w
?IIえばカーペットのバッキング剤に用いる場合には
、従来のバッキング剤を使用した場合に比してバッキン
グ剤のx4が約1/3となり、カーペットを含む全重蓋
は33〜42係も軽くすることが可能となる。Thus, the SBR latex composition according to the present invention''*w
? II.For example, when used as a backing agent for carpets, the x4 of the backing agent will be approximately 1/3 compared to when using a conventional backing agent, and the full heavy lid including the carpet will be 33 to 42 parts lighter. becomes possible.
又、カーペットに使用した場合これを折り曲げてもバッ
キング剤部分にヒビが入ることがなく、屈曲性を向上で
き、更に吸音性も向上すると云う意外な効果の他、断熱
性も同上し得る等のオ0点がある。又、従来の発泡コン
パウンドの様に脱泡等による北東変化、粘匣変化叫がな
く保存性がすぐれている。In addition, when used on carpets, the backing material does not crack even when folded, improving flexibility and sound absorption, which is an unexpected effect, as well as insulation properties. I have 0 points. In addition, unlike conventional foaming compounds, there is no northeast change or viscous change due to defoaming, and the product has excellent storage stability.
本発明によるSBRラテックス組成物には、上記中空体
の他、所望によシ増粘剤、消泡剤、顔料等、本発明の目
的を阻害しない限9種々の察加物を添加することができ
る。In addition to the above-mentioned hollow bodies, the SBR latex composition according to the present invention may contain nine various additives, such as thickeners, antifoaming agents, pigments, etc., as long as they do not impede the object of the present invention. can.
次に本発明を実施例にょシ説明する。Next, the present invention will be explained using examples.
SDRラテックス(旭ダウ社製I、−2135)固形分
換算100重重部に粒径2o〜200μを有するシリカ
系中空体(グラバ−ベル社製M−28)に、γ−メタア
クロキシグロビルトリメトキシシラン処理したもの・4
4重敷部、ポリアクリル敏ンーダ系増粘刑(東亜合成、
化学社製アロンA −20P ) I N型部、シリコ
ンオイルエマルショア (束LylQB M 5512
) 0.1に置部、合成ポリカルボン酸塙(東亜合成
化学社製アロンAS−6310)1.5n式部娑蛤≧刀
口混合し、BL型粘度計6 r、pm (25℃)によ
り長期安定性を観察した処、脚製厘後は24000c、
pであり1ケ月俊には28000C,1)でりった。SDR latex (manufactured by Asahi Dow Co., Ltd. I, -2135) 100 parts by weight in terms of solid content contains silica-based hollow bodies (M-28, manufactured by Grabber Bell Co., Ltd.) having a particle size of 2o to 200μ, and Methoxysilane treated ・4
4 layers, polyacrylic resin thickener (Toagosei,
Aron A-20P manufactured by Kagakusha) I N type part, silicone oil emulsion (bundle LylQB M 5512
) 0.1, synthetic polycarboxylic acid (Aron AS-6310 manufactured by Toagosei Kagaku Co., Ltd.) 1.5n Shikibu Sakahama ≧ Toguchi mixed, and long-term measurement using a BL type viscometer at 6 r, pm (25°C). When I observed the stability, after making the legs it was 24000c,
It was 28,000C, 1) for 1 month Shun.
これに対し、上記中を体を表面処理することなく同量用
いた以外同様に調製して同様に観察した処、ルー製直後
は24000C,1)であシ1ケ月後には44000(
!、pを示した。On the other hand, when the same amount of the above medium was prepared and observed in the same manner without surface treatment of the body, it was 24000C, 1) immediately after making the roux, and 44000C (1) after one month.
! , p was shown.
調製後における粘度質化は4000c、p以内でないと
、例えばカーペットにつくバッキング剤量が変化し、品
質官理が困難になるので、本発明のラテックスが優れて
いることが理解される。It is understood that the latex of the present invention is superior because if the viscosity after preparation is not within 4000 c.p, the amount of backing agent attached to the carpet will change, making quality control difficult.
又、本発明のラテックスの比重は1ケ月後においても変
化なく 0.71であシ、比較例品は調製血抜の0.7
1から1ケ月後には098と高くなっており、ラテック
ス自体の比重1.0に接近しているのに対し、本発明の
ラテックスが軽重化されていることも理解される。In addition, the specific gravity of the latex of the present invention did not change even after one month, which was 0.71, and the comparative example product had a specific gravity of 0.7 after blood removal.
One month later, the specific gravity was as high as 098, which is close to the specific gravity of the latex itself, which is 1.0, and it is also understood that the latex of the present invention is lighter in weight.
275−275-
Claims (1)
のない無機質の微小中空体を混入せしめたことを特徴と
するSBRラテックス組成物。 2、 微小中空体は平均粒径10〜300μである請求
の範囲(1)の組成物。 3 無機質の微小中空体は、その表面を撒水処理したも
のである請求の範囲(1)又は(2)の組成物。 4 無機質の微小中空体の混入量は、ラテックスの固形
分100M量部に対し、10〜501量部である請求の
範囲(1)の組成物。1.8 An SBR latex composition characterized in that inorganic micro hollow bodies having substantially no water absorption or solubility are mixed into BR latex. 2. The composition according to claim (1), wherein the micro hollow bodies have an average particle size of 10 to 300μ. 3. The composition according to claim (1) or (2), wherein the inorganic micro hollow bodies have surfaces treated with water spraying. 4. The composition according to claim (1), wherein the amount of the inorganic micro hollow bodies mixed is 10 to 501 parts by weight based on 100 M parts of the solid content of the latex.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57219242A JPS59109540A (en) | 1982-12-16 | 1982-12-16 | Sbr latex composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57219242A JPS59109540A (en) | 1982-12-16 | 1982-12-16 | Sbr latex composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59109540A true JPS59109540A (en) | 1984-06-25 |
Family
ID=16732438
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57219242A Pending JPS59109540A (en) | 1982-12-16 | 1982-12-16 | Sbr latex composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59109540A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63225657A (en) * | 1986-10-28 | 1988-09-20 | Calp Corp | Composite polymer composition |
FR2926473A1 (en) * | 2008-01-22 | 2009-07-24 | Commissariat Energie Atomique | COATED AND FUNCTIONALIZED PARTICLES, POLYMER CONTAINING THEM, PROCESS FOR PREPARING THEM AND USES THEREOF |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4710526A (en) * | 1970-11-20 | 1972-05-26 | ||
JPS57108147A (en) * | 1980-11-07 | 1982-07-06 | Du Pont | Product and production |
-
1982
- 1982-12-16 JP JP57219242A patent/JPS59109540A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4710526A (en) * | 1970-11-20 | 1972-05-26 | ||
JPS57108147A (en) * | 1980-11-07 | 1982-07-06 | Du Pont | Product and production |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63225657A (en) * | 1986-10-28 | 1988-09-20 | Calp Corp | Composite polymer composition |
FR2926473A1 (en) * | 2008-01-22 | 2009-07-24 | Commissariat Energie Atomique | COATED AND FUNCTIONALIZED PARTICLES, POLYMER CONTAINING THEM, PROCESS FOR PREPARING THEM AND USES THEREOF |
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