JP2005120273A - Puncture sealing agent for tire - Google Patents
Puncture sealing agent for tire Download PDFInfo
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- JP2005120273A JP2005120273A JP2003358165A JP2003358165A JP2005120273A JP 2005120273 A JP2005120273 A JP 2005120273A JP 2003358165 A JP2003358165 A JP 2003358165A JP 2003358165 A JP2003358165 A JP 2003358165A JP 2005120273 A JP2005120273 A JP 2005120273A
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- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Tires In General (AREA)
- Sealing Material Composition (AREA)
Abstract
Description
本発明は、長期間保管する際のクリーム状物質の生成を抑え、保管性能(経時安定性)を高めたタイヤのパンクシーリング剤に関する。 The present invention relates to a tire puncture sealant that suppresses the formation of a cream-like substance during long-term storage and has improved storage performance (stability over time).
タイヤにパンクが発生したとき、空気バルブからタイヤ内に注入することによってパンク穴を応急的に修理するパンクシーリング剤として、天然ゴムラテックスに、粘着付与樹脂エマルジョンとグリコールからなる凍結防止剤とを配合したものが多用されている。 When a puncture occurs in a tire, a natural rubber latex is combined with an antifreezing agent consisting of glycol and a natural rubber latex as a puncture sealant that repairs a puncture hole by injecting it into the tire through an air valve. What was done is used a lot.
しかし、この種のパンクシーリング剤では、長期間保管したとき、その中のゴム粒子が表面付近で凝集してクリーム状物質へと変質し、パンクシール性能を低下させる傾向にある。 However, when this type of puncture sealing agent is stored for a long period of time, the rubber particles therein tend to aggregate near the surface and transform into a creamy substance, which tends to lower the puncture sealing performance.
なお、このクリーム状物質の発生メカニズムは、以下の如くと推測される。即ち、パンクシーリング剤は、凍結防止剤であるグリコール(例えばエチレングリコール)の水溶液中に、ゴム粒子と粘着付与樹脂粒子とがイオン斥力によって反発しあって分散浮遊しているエマルジョンであるが、ゴム粒子の比重が、分散媒であるグリコール水溶液よりも小さいため、重力の作用によってゴム粒子が分散媒中をしだいに浮上していき、これが表面付近で濃縮層を形成し、クリーム状物質を生成すると推測される。 In addition, the generation | occurrence | production mechanism of this cream-like substance is estimated as follows. In other words, the puncture sealant is an emulsion in which rubber particles and tackifying resin particles are repelled by ionic repulsion and suspended in an aqueous solution of an antifreeze glycol (eg, ethylene glycol). Since the specific gravity of the particles is smaller than that of the aqueous glycol solution, which is the dispersion medium, the rubber particles gradually rise in the dispersion medium due to the action of gravity, and this creates a concentrated layer near the surface, producing a cream-like substance. Guessed.
そのため、例えば増粘剤を添加することにより分散媒の粘度を高める(特許文献1参照)ことにより、ゴム粒子の浮上速度を抑えてクリーム状物質の生成を抑制ことが提案されている。 Therefore, for example, by increasing the viscosity of the dispersion medium by adding a thickener (see Patent Document 1), it has been proposed to suppress the rising speed of the rubber particles and suppress the formation of a cream-like substance.
しかし、前記粘度を高める手段では、パンクシーリング剤のタイヤへの注入が難しくなるという問題がある。 However, the means for increasing the viscosity has a problem that it becomes difficult to inject the puncture sealant into the tire.
そこで本発明は、天然ゴムラテックスとして、ゴム粒子中に粒子径が0.5μm以下の微細ゴム粒子を所定割合で含むものを使用することを基本として、ゴム粒子のブラウン運動を活発化せしめ、その分散性を高めることによりゴム粒子の分散媒中での浮上、凝集を抑えることができ、パンクシール性能を損ねることなく、かつ前記問題を招くことなく、保管時におけるクリーム状物質の生成を低く抑制しうるタイヤのパンクシーリング剤を提供することを目的としている。 Therefore, the present invention activates the Brownian motion of rubber particles based on the use of natural rubber latex containing rubber particles containing fine rubber particles having a particle size of 0.5 μm or less in a predetermined ratio. By increasing dispersibility, the floating and aggregation of rubber particles in the dispersion medium can be suppressed, and the generation of cream-like substances during storage is suppressed to a low level without impairing the puncture sealing performance and causing the above problems. An object of the present invention is to provide a tire puncture sealant that can be used.
前記目的を達成するために、本願請求項1の発明は、天然ゴムラテックスと、粘着付与樹脂エマルジョンと、グリコールからなる凍結防止剤とを含むタイヤのパンクシーリング剤であって、
前記天然ゴムラテックスは、ゴム粒子中に、粒子径が0.5μm以下の微細ゴム粒子を含み、かつ該微細ゴム粒子の粒子数を全ゴム粒子数の55%以上としたことを特徴としている。
In order to achieve the above object, the invention of claim 1 of the present application is a tire puncture sealing agent comprising a natural rubber latex, a tackifying resin emulsion, and an antifreezing agent comprising glycol,
The natural rubber latex is characterized in that the rubber particles contain fine rubber particles having a particle size of 0.5 μm or less, and the number of fine rubber particles is 55% or more of the total number of rubber particles.
又請求項2の発明では、前記天然ゴムラテックスは、脱蛋白ゴムラテックスであることを特徴としている。 The invention according to claim 2 is characterized in that the natural rubber latex is deproteinized rubber latex.
又請求項3の発明では、前記凍結防止剤は、エチレングリコールまたはプロピレングリコールであり、かつパンクシーリング剤の全重量に対し20〜35重量%含まれることを特徴としている。 The invention of claim 3 is characterized in that the antifreezing agent is ethylene glycol or propylene glycol and is contained in an amount of 20 to 35% by weight based on the total weight of the puncture sealing agent.
本発明は叙上の如く構成しているため、ゴム粒子のブラウン運動の活発化によって、ゴム粒子の分散媒中での浮上、凝集を抑えることができ、パンクシール性能を損ねることなく、保管時におけるクリーム状物質の生成を低く抑制することが可能となる。 Since the present invention is configured as described above, the activation of the Brownian motion of the rubber particles can prevent the rubber particles from floating and agglomerating in the dispersion medium, and the puncture sealing performance is not impaired. It becomes possible to suppress the production | generation of the creamy substance in low.
以下、本発明の実施の一形態を、図示例とともに説明する。
本発明のタイヤのパンクシーリング剤は、ゴムラテックスと、粘着付与樹脂エマルジョンと、グリコールからなる凍結防止剤とを少なくとも含んで構成される。
Hereinafter, an embodiment of the present invention will be described with reference to the drawings.
The tire puncture sealant of the present invention comprises at least rubber latex, a tackifying resin emulsion, and an antifreezing agent composed of glycol.
前記ゴムラテックスとして、本発明では、シール性能の高い天然ゴムラテックスを採用するが、特に、この天然ゴムラテックスから蛋白質を除去した所謂脱蛋白天然ゴムラテックスは、より少ないアンモニアで腐敗を抑えることができるため、アンモニアに起因するスチールコードへの腐食損傷及び刺激臭の発生を防止するという観点から、より好ましく採用できる。 As the rubber latex, natural rubber latex having high sealing performance is used in the present invention. In particular, so-called deproteinized natural rubber latex obtained by removing protein from natural rubber latex can suppress spoilage with less ammonia. Therefore, the steel cord can be more preferably employed from the viewpoint of preventing corrosion damage to the steel cord caused by ammonia and generation of an irritating odor.
ここで、前記天然ゴムラテックスは、周知の如く、乳化剤である界面活性剤を少量含む水性媒体(分散媒)中に、ゴム固形分をゴム粒子のかたちで分散させた懸濁液であり、走行により速やかにパンク穴に入り込み、このパンク穴を塞ぎ、かつある程度の走行距離までパンクシール性能を保持させるために、前記ゴム固形分のパンクシーリング剤の全重量に対する配合量Aを25〜40重量%の範囲とするのが好ましい。なお配合量Aを前記範囲に確保するために、天然ゴムラテックスに占めるゴム固形分の含有量を60重量%程度まで高めた濃縮型天然ゴムラテックスが使用される。 Here, the natural rubber latex is a suspension in which rubber solids are dispersed in the form of rubber particles in an aqueous medium (dispersion medium) containing a small amount of a surfactant as an emulsifier, as is well known. In order to quickly enter the puncture hole, close the puncture hole, and maintain the puncture sealing performance up to a certain travel distance, the blending amount A with respect to the total weight of the puncture sealing agent of the rubber solid content is 25 to 40% by weight. It is preferable to be in the range. In order to secure the blending amount A within the above range, a concentrated natural rubber latex having a rubber solid content in the natural rubber latex increased to about 60% by weight is used.
次に、粘着付与樹脂エマルジョンは、ゴムラテックスと同様、乳化剤を少量含む水性媒体中に、粘着付与樹脂を微粒子状に分散させた水中油滴型エマルジョンであって、その固形分である粘着付与樹脂としては、前記天然ゴムラテックスを凝固させないもの、例えばテルペン系樹脂、フェノール系樹脂、ロジン系樹脂が好ましく使用できる。他に好ましい樹脂としては、ポリビニルエステル、ポリビニルアルコール、およびポリビニルピロリジンがある。 Next, the tackifying resin emulsion is an oil-in-water emulsion in which the tackifying resin is dispersed in the form of fine particles in an aqueous medium containing a small amount of an emulsifier, like rubber latex, and the tackifying resin is a solid content thereof. For example, those that do not coagulate the natural rubber latex, such as terpene resins, phenol resins, and rosin resins, can be preferably used. Other preferred resins include polyvinyl esters, polyvinyl alcohol, and polyvinyl pyrrolidine.
この粘着付与樹脂は、天然ゴムラテックスとタイヤとの接着性を高め、パンクシール性能を向上させるために用いられるものであり、その配合量Bは、パンクシーリング剤の全重量に対し、10〜30重量%が好ましい。なお前記ゴム固形分の配合量Aが25重量%未満、及び粘着付与樹脂の配合量Bが10重量%未満では、パンクシール性能及びそれを保持する性能(シール保持性能)が不十分となる。逆に各配合量A、Bがそれぞれ40重量%、及び30重量%を越えると、保管中にゴム粒子が凝集しやすくなるなど保管性能を損ねるとともに、粘度が上昇しパンクシーリング剤の空気バルブからの注入を難しくさせる。従って、前記配合量A、Bの和(A+B)をパンクシーリング剤の全重量に対し35〜60重量%に規制するのも好ましい。 This tackifying resin is used for enhancing the adhesion between the natural rubber latex and the tire and improving the puncture sealing performance, and its blending amount B is 10-30 with respect to the total weight of the puncture sealing agent. % By weight is preferred. In addition, when the compounding amount A of the rubber solid content is less than 25% by weight and the compounding amount B of the tackifying resin is less than 10% by weight, the puncture sealing performance and the performance of retaining it (seal retaining performance) are insufficient. On the other hand, if the blending amounts A and B exceed 40% by weight and 30% by weight, respectively, the storage performance is impaired such as the rubber particles tend to aggregate during storage, and the viscosity increases and the air valve of the puncture sealant increases. Makes injection difficult. Therefore, it is also preferable to regulate the sum (A + B) of the blending amounts A and B to 35 to 60% by weight with respect to the total weight of the puncture sealing agent.
なお前記天然ゴムラテックスの乳化剤、及び粘着付与樹脂エマルジョンの乳化剤としては、例えばアニオン性界面活性剤、非イオン性界面活性剤、カチオン性界面活性剤などの種々の界面活性剤が好適に使用できる。この乳化剤の総配合量は、パンクシーリング剤の全重量に対し0.4〜2.0重量%程度である。 As the emulsifier for the natural rubber latex and the emulsifier for the tackifying resin emulsion, various surfactants such as an anionic surfactant, a nonionic surfactant, and a cationic surfactant can be preferably used. The total amount of the emulsifier is about 0.4 to 2.0% by weight with respect to the total weight of the puncture sealing agent.
次に、前記凍結防止剤としては、例えばエチレングリコール、ジエチレングリコール、プロピレングリコール、トリエチレングリコールなどのグリコール(二価アルコール)が使用できる。このうち、凍結防止効果に優れるエチレングリコール、およびプロピレングリコールは、その使用量を最小限に抑えることができ、凍結防止剤によるパンクシール性能等の諸特性への悪影響を防止するうえで好ましい。 Next, as the antifreezing agent, for example, glycols (dihydric alcohols) such as ethylene glycol, diethylene glycol, propylene glycol, and triethylene glycol can be used. Of these, ethylene glycol and propylene glycol, which are excellent in antifreezing effect, can be used in a minimum amount, and are preferable for preventing adverse effects on various properties such as puncture sealing performance by the antifreezing agent.
なお凍結防止剤として、エチレングリコール及びプロピレングリコールを使用する場合、パンクシーリング剤の全重量に対する配合量Cを、20〜35重量%の範囲とするのが好ましく、これによって、パンクシーリング剤の凍結温度を例えば−30℃以下の低温にまで下げることが可能となる。 When ethylene glycol and propylene glycol are used as antifreeze agents, the blending amount C with respect to the total weight of the puncture sealing agent is preferably in the range of 20 to 35% by weight, whereby the freezing temperature of the puncture sealing agent is reduced. Can be lowered to a low temperature of, for example, −30 ° C. or lower.
そして本発明では、パンクシーリング剤を長期間保管した際にゴム粒子が凝集してクリーム状物質が生成されるのを抑制するため、天然ゴムラテックスとして、ゴム粒子中に、粒子径が0.5μm以下の微細ゴム粒子を、全ゴム粒子数に対して55%以上含有させた微粒子ゴムラテックスを採用している。なお微細ゴム粒子の粒子数の全ゴム粒子数に対する割合を、便宜上、粒子数%と呼ぶ場合がある。又ゴムラテックス中に分散するゴム粒子の粒子径、及び粒子径の分布は、光散乱光度計を用いて測定することができるため、その測定結果から、前記粒子径0.5μm以下である微細ゴム粒子の粒子数%を求めることができる。 In the present invention, when the puncture sealant is stored for a long period of time, in order to prevent the rubber particles from agglomerating to produce a cream-like substance, the natural rubber latex has a particle diameter of 0.5 μm in the rubber particles. Fine rubber latex containing 55% or more of the following fine rubber particles with respect to the total number of rubber particles is employed. The ratio of the number of fine rubber particles to the total number of rubber particles may be referred to as the number of particles% for convenience. The particle size of the rubber particles dispersed in the rubber latex and the particle size distribution can be measured using a light scattering photometer. From the measurement results, the fine rubber having a particle size of 0.5 μm or less is used. The number% of particles can be determined.
ここで、本発明者が研究した結果、粒子径0.5μm以下の微細ゴム粒子は、ブラウン運動が活発であるため分散性が高く、特に、その粒子数%を55%以上、好ましくは60%以上に増加させた場合には、他のゴム粒子もこの微細ゴム粒子の影響を受けて全体としての分散性を高めることができ、保管中のゴム粒子の浮上凝集を低く抑え、クリーム状物質の生成を抑制しうることを見出し得た。 Here, as a result of the study by the present inventor, fine rubber particles having a particle size of 0.5 μm or less have high dispersibility due to active Brownian motion. In particular, the number of particles is 55% or more, preferably 60%. When the amount is increased as described above, the other rubber particles are also affected by the fine rubber particles, so that the overall dispersibility can be improved. It has been found that the production can be suppressed.
なお前記ゴム粒子において、粒子径0.5μm以下のゴム微粒子の粒子数%が55%未満の場合にはゴム粒子全体の分散性を充分に高めることが難しく、クリーム状物質の生成抑制を発揮することができなくなる。また前記ゴム粒子における粒子径が0.5μm以下であるゴム微粒子の粒子数%の上限の値は規定されないが、微粒子の粒子数の%が高すぎると製造効率及び製造コストに不利であり、また高い固形分では粘度が上昇する問題がある。そのためゴム粒子中の0.5μm以下の粒子数%の上限は75%以下が好ましい。 In the rubber particles, when the number of particles of rubber fine particles having a particle diameter of 0.5 μm or less is less than 55%, it is difficult to sufficiently increase the dispersibility of the entire rubber particles, and the production of creamy substances is suppressed. I can't do that. The upper limit value of the number of particles of rubber fine particles having a particle diameter of 0.5 μm or less in the rubber particles is not specified, but if the percentage of the number of fine particles is too high, it is disadvantageous for production efficiency and production cost. There is a problem that the viscosity increases at a high solid content. Therefore, the upper limit of the number% of particles of 0.5 μm or less in the rubber particles is preferably 75% or less.
ここで、本発明者の調査によると、ゴム樹から採取されたフィールドゴムラテックスにおいては、一般に、粒子径0.5μm以下の微細ゴム粒子が、全ゴム粒子数の60%以上含まれているが、このフィールドゴムラテックスを濃縮したゴム固形分約60重量%の濃縮ラテックスでは、微細ゴム粒子の粒子数%が55%以下にまで減少していることが判明した。その原因として、フィールドゴムラテックスの濃縮方法が挙げられる。即ち、フィールドゴムラテックスの濃縮には、通常、遠心分離法が採用されるが、この遠心分離法においては、微細ゴム粒子の多くが分離されずに漿液中に残存し、分離された濃縮ラテックス中の微細ゴム粒子を減少させる。 Here, according to the inventor's investigation, the field rubber latex collected from the rubber tree generally contains fine rubber particles having a particle diameter of 0.5 μm or less of 60% or more of the total number of rubber particles. In the concentrated latex having a rubber solid content of about 60% by weight obtained by concentrating the field rubber latex, it was found that the number of fine rubber particles was reduced to 55% or less. The cause is the concentration method of field rubber latex. That is, for the concentration of the field rubber latex, a centrifugal separation method is usually employed. In this centrifugal separation method, most of the fine rubber particles remain in the serum without being separated, and in the separated concentrated latex. Reduces fine rubber particles.
従って、本発明に使用される微粒子ゴムラテックスは、特に規制されないが例えば、
(1)遠心分離法以外の濃縮方法でフィールドゴムラテックスを濃縮させる;又は
(2)遠心分離時に得られる漿液から微細ゴム粒子を回収し、これを遠心分離の濃縮ラテックス、或いは他の濃縮ラテックスに添加する;
ことによって形成することができる。
Therefore, the fine particle rubber latex used in the present invention is not particularly restricted, for example,
(1) Concentrate the field rubber latex by a concentration method other than the centrifugation method; or (2) Collect fine rubber particles from the serum obtained at the time of centrifugation, and use this to collect the concentrated latex in the centrifugation or other concentrated latex. Added;
Can be formed.
なお以下に、前記(1)、(2)の方法を用いて、脱蛋白処理した濃縮の微粒子ゴムラテックスを精製する場合を例示する。
まずフィールドゴムラテックス(固形分30重量%)に、蛋白分解酵素を添加し蛋白質を分解させた脱蛋白ゴムラテックスを形成する。蛋白分解用酵素としては、例えば細菌由来のもの、糸状菌由来のもの、酵母由来のものなどのいずれであってもよく、特に限定されるものではないが、細菌由来のプロテアーゼを使用するのが好ましい。かかる蛋白分解用酵素による分解処理は、通常、フィールドゴムラテックスに対し蛋白分解用酵素を0.01〜10重量%の割合で添加し、数時間ないし1週間静置または攪拌することにより行うことができる。蛋白分解処理は、5〜90℃、好ましくは20〜60℃の温度で行うのが適当である。
An example of purifying concentrated fine particle rubber latex that has been deproteinized using the methods (1) and (2) will be described below.
First, a deproteinized rubber latex is formed by adding a proteolytic enzyme to a field rubber latex (solid content: 30% by weight) to decompose proteins. The enzyme for proteolysis may be any of, for example, those derived from bacteria, those derived from filamentous fungi, those derived from yeasts, and is not particularly limited. preferable. Such a degradation treatment with a proteolytic enzyme is usually carried out by adding 0.01 to 10% by weight of the proteolytic enzyme to the field rubber latex and allowing it to stand or stir for several hours to one week. it can. Proteolytic treatment is suitably performed at a temperature of 5 to 90 ° C, preferably 20 to 60 ° C.
又前記にて得た脱蛋白ゴムラテックスを、特開平7−238102号公報に記載の回転式平膜分離装置を用いた回転式平膜分離法により濃縮する。これにより、微細ゴム粒子の含有量を高く維持した状態のまま、固形分約60重量%の濃縮の微粒子ゴムラテックスを得ることができる。 The deproteinized rubber latex obtained above is concentrated by a rotary flat membrane separation method using a rotary flat membrane separator described in JP-A-7-238102. As a result, a concentrated fine rubber latex having a solid content of about 60% by weight can be obtained while maintaining a high content of fine rubber particles.
或いは前記にて得た脱蛋白ゴムラテックスを、特開平11−106405号公報に記載のクリーム化剤を用いたクリーミング分離法により濃縮することにより、微細ゴム粒子の含有量を高く維持した状態のまま、固形分約60重量%の濃縮の微粒子ゴムラテックスを得ることができる。このときクリーム化剤として、例えばアルギン酸ナトリウム(アルギン酸ソーダ)、アルギン酸アンモニウム、こんにゃく糊(マンナン)、トラカガントゴム(トラガント)等を使用し、かつ前記クリーム化剤を、前記脱蛋白ゴムラテックスに対して0.1〜1phr添加する。これにより、漿液側に微細ゴム粒子を移行させることなく、略全てのゴム粒子をクリーム層として漿液と分離することができる。 Alternatively, the deproteinized rubber latex obtained above is concentrated by a creaming separation method using a creaming agent described in JP-A-11-106405, so that the content of the fine rubber particles is kept high. Thus, a concentrated fine rubber latex having a solid content of about 60% by weight can be obtained. At this time, as a creaming agent, for example, sodium alginate (sodium alginate), ammonium alginate, konjac paste (mannan), tragagant gum (tragacanth), etc., and the creaming agent is added to the deproteinized rubber latex by 0. Add 1-1 phr. Thereby, substantially all rubber particles can be separated from the serum as a cream layer without transferring the fine rubber particles to the serum side.
次に、遠心分離時に得られる漿液を利用する方法を説明する。まず前記にて得た脱蛋白ゴムラテックスを、従来の遠心分離法によって濃縮する。このとき漿液中には、微細ゴム粒子の多くが分離されずに残存する。従って、この漿液に含まれる微細ゴム粒子を濃縮し、前記遠心分離の濃縮ラテックスに戻すことにより、微細ゴム粒子の含有量の高い濃縮の微粒子ゴムラテックスを得ることができる。なお、初期のフィールドゴムラテックスにおいて、微細ゴム粒子の粒子数%が55%に満たない場合には、前記漿液から濃縮した微細ゴム粒子を、前記回転式平膜分離法、及びクリーミング分離法で得た微粒子ゴムラテックスに添加することにより、微細ゴム粒子の粒子数%を55%以上に設定することができる。 Next, a method using the serum obtained at the time of centrifugation will be described. First, the deproteinized rubber latex obtained above is concentrated by a conventional centrifugation method. At this time, most of the fine rubber particles remain in the serum without being separated. Therefore, concentrated fine rubber particles having a high content of fine rubber particles can be obtained by concentrating the fine rubber particles contained in the serum and returning to the concentrated latex of the centrifugal separation. In the initial field rubber latex, when the number of fine rubber particles is less than 55%, fine rubber particles concentrated from the serum are obtained by the rotary flat membrane separation method and the creaming separation method. By adding to the fine rubber latex, the number of fine rubber particles can be set to 55% or more.
なお前記漿液の濃縮法として、前記回転式平膜分離法、及びクリーミング分離法が好適である。又遠心分離法も採用しうるが、このときには、分離効果を確保するため、比重の高い水溶性化合物(例えばグリコール類)を漿液に添加する必要があり、又この水溶性化合物のゴム中への混入を抑えるため、回転数を高める及び遠心分離時の滞留時間を長くするのが好ましい。 As the serum concentration method, the rotary flat membrane separation method and the creaming separation method are suitable. Centrifugation may also be employed, but in this case, in order to ensure the separation effect, it is necessary to add a water-soluble compound having a high specific gravity (for example, glycols) to the serum, and this water-soluble compound is added to the rubber. In order to suppress mixing, it is preferable to increase the rotation speed and lengthen the residence time during centrifugation.
以上、本発明の特に好ましい実施形態について詳述したが、上述の実施形態に限定されることなく、種々の態様に変形して実施しうる。 As mentioned above, although especially preferable embodiment of this invention was explained in full detail, it is not limited to the above-mentioned embodiment, It can deform | transform and implement in a various aspect.
表1の仕様に基づきパンクシール剤を試作するとともに、各試供品のパンクシール性能、シール保持性能、保管性能を測定し、従来例1,2と比較するとともに、その結果を表1に記載した。 While producing a puncture sealant on the basis of the specifications in Table 1, the puncture seal performance, seal retention performance, and storage performance of each sample were measured, and compared with Conventional Examples 1 and 2, and the results are shown in Table 1. .
表1中、各ゴムラテックスGa〜Ge(固形分60重量%)は、以下の方法で形成された。
・ ゴムラテックスGaは、フィールドゴムラテックス(固形分30重量%)を、遠心分離法を用いて濃縮することにより形成した。
・ ゴムラテックスGbは、前記フィールドゴムラテックス(固形分30重量%)に、細菌由来の蛋白分解酵素を添加し、40℃−24時間放置して蛋白質を分解させた脱蛋白ゴムラテックスを得るとともに、この脱蛋白ゴムラテックスを、遠心分離法を用いて濃縮することにより形成した。
・ ゴムラテックスGcは、前記と同様の手法で得た脱蛋白ゴムラテックスを、回転式平膜分離法を用いて濃縮することにより形成した。
・ ゴムラテックスGdは、前記と同様の手法で得た脱蛋白ゴムラテックスを、クリーミング分離法(クリーム化剤としてアルギン酸ナトリウムを0.5phr添加)を用いて濃縮することにより形成した。
・ ゴムラテックスGeは、前記と同様の手法で得た脱蛋白ゴムラテックスを、遠心分離法を用いて濃縮するとともに、そのとき生じる漿液中の微細ゴム粒子を濃縮し、前記遠心分離のゴムラテックスに戻すことにより形成した。
In Table 1, each rubber latex Ga to Ge (solid content 60% by weight) was formed by the following method.
The rubber latex Ga was formed by concentrating field rubber latex (solid content 30% by weight) using a centrifugal separation method.
The rubber latex Gb is obtained by adding a bacterial protease derived from the field rubber latex (solid content 30% by weight) and leaving it at 40 ° C. for 24 hours to decompose the protein, thereby obtaining a deproteinized rubber latex. This deproteinized rubber latex was formed by concentrating using a centrifugation method.
The rubber latex Gc was formed by concentrating a deproteinized rubber latex obtained by the same method as described above using a rotary flat membrane separation method.
The rubber latex Gd was formed by concentrating the deproteinized rubber latex obtained by the same method as described above using a creaming separation method (adding 0.5 phr of sodium alginate as a creaming agent).
The rubber latex Ge is obtained by concentrating the deproteinized rubber latex obtained by the same method as described above by using a centrifugal separation method, concentrating fine rubber particles in the serum, and forming the rubber latex of the centrifugal separation. Formed by returning.
又各ゴムラテックスGa〜Geにおいて、粒子径0.5μm以下の微細ゴム粒子の粒子数%は、光散乱光度計を用いて測定した。 In each rubber latex Ga to Ge, the number% of fine rubber particles having a particle diameter of 0.5 μm or less was measured using a light scattering photometer.
(1)パンクシール性能:
タイヤサイズ185/65R14のタイヤに、直径4.0mmの釘で穴を開け、釘を抜いた後、500mlのパンクシーリング剤を注入しかつエアーを200kpaまで昇圧した。しかる後、ドラム上で荷重(3.5kN)にて回転させ、パンク穴がシールされるまでの時間をエアー漏れの量で判断し、従来例1を3とした5段階で指数評価した。値が大なほど優れている。
(1) Punk seal performance:
A tire having a tire size of 185 / 65R14 was drilled with a nail having a diameter of 4.0 mm, the nail was pulled out, 500 ml of a puncture sealant was injected, and the air pressure was increased to 200 kpa. Thereafter, the drum was rotated at a load (3.5 kN) on the drum, and the time until the puncture hole was sealed was judged based on the amount of air leakage. The higher the value, the better.
(2)シール保持性能:
前記タイヤを用い、シールされてから100km走行するまでにパンク穴からエアー漏れがあったかどうかを測定したものであり、エアー漏れなし…○、エアー漏れあり…×、の2段階で評価した。
(2) Seal retention performance:
The tire was used to measure whether or not there was an air leak from a puncture hole before traveling 100 km after being sealed, and was evaluated in two stages: no air leak ... ○, air leak ... ×.
(3)保管性能(経時安定性):
試作したパンクシーリング剤を期間(10日間)、温度(70゜C)の条件下で放置した際に生成されたクリーム物質をフィルタを用いて取り、パンクシール剤全体に対する体積比で示した。又括弧内には、前記体積比を従来例1を100とする値で示している。夫々値が小なほど優れている。
(3) Storage performance (stability over time):
The cream substance produced when the prototype puncture sealing agent was allowed to stand under the conditions of a period (10 days) and temperature (70 ° C.) was taken out using a filter and indicated by volume ratio with respect to the whole puncture sealing agent. In the parentheses, the volume ratio is shown as a value with the conventional example 1 being 100. The smaller the value, the better.
表の如く、実施例のパンクシーリング剤は、パンクシール性能、シール保持性能を維持しながら、クリーム物質の生成を抑え、保管性能(経時安定性)を向上しうるのが確認できる。 As shown in the table, it can be confirmed that the puncture sealing agents of the examples can suppress the formation of cream substance and improve the storage performance (stability over time) while maintaining the puncture sealing performance and seal retention performance.
Claims (3)
前記天然ゴムラテックスは、ゴム粒子中に、粒子径が0.5μm以下の微細ゴム粒子を含み、かつ該微細ゴム粒子の粒子数を全ゴム粒子数の55%以上としたことを特徴とするタイヤのパンクシーリング剤。 A tire puncture sealing agent comprising a natural rubber latex, a tackifying resin emulsion, and an antifreezing agent comprising glycol,
The natural rubber latex includes fine rubber particles having a particle diameter of 0.5 μm or less in rubber particles, and the number of fine rubber particles is 55% or more of the total number of rubber particles. Puncture sealant.
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JP2011006646A (en) * | 2009-06-29 | 2011-01-13 | Sumitomo Rubber Ind Ltd | Puncture sealing agent |
JP2015513078A (en) * | 2012-02-16 | 2015-04-30 | コンパニー ゼネラール デ エタブリッスマン ミシュラン | Method for inspecting tire resistance to pressure drop |
CN104364341A (en) * | 2012-06-27 | 2015-02-18 | 住友橡胶工业株式会社 | Puncture sealing agent |
WO2014003028A1 (en) * | 2012-06-27 | 2014-01-03 | 住友ゴム工業株式会社 | Puncture sealing agent |
CN104364341B (en) * | 2012-06-27 | 2016-07-06 | 住友橡胶工业株式会社 | Mending agent |
US9617442B2 (en) | 2012-06-27 | 2017-04-11 | Sumitomo Rubber Industries, Ltd. | Puncture sealing agent |
US20160168431A1 (en) * | 2014-12-12 | 2016-06-16 | Illinois Tool Works Inc. | High performance sealant composition for tire repair |
US10208231B2 (en) * | 2014-12-12 | 2019-02-19 | Illinois Tool Works, Inc. | High performance sealant composition for tire repair |
CN107428097A (en) * | 2015-01-16 | 2017-12-01 | 伊利诺斯工具制品有限公司 | High-performance sealed agent composition for tyre repair |
US20160289509A1 (en) * | 2015-04-01 | 2016-10-06 | Illinois Tool Works Inc. | High performance enviromentally friendly sealant composition for tire repair |
US9963620B2 (en) * | 2015-04-01 | 2018-05-08 | Illinois Tool Works Inc. | High performance environmentally friendly sealant composition for tire repair |
JP2021138848A (en) * | 2020-03-05 | 2021-09-16 | 住友ゴム工業株式会社 | Puncture sealant |
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