JP2010260885A5 - - Google Patents

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Publication number
JP2010260885A5
JP2010260885A5 JP2009110354A JP2009110354A JP2010260885A5 JP 2010260885 A5 JP2010260885 A5 JP 2010260885A5 JP 2009110354 A JP2009110354 A JP 2009110354A JP 2009110354 A JP2009110354 A JP 2009110354A JP 2010260885 A5 JP2010260885 A5 JP 2010260885A5
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JP
Japan
Prior art keywords
mixing
latex
antifreeze
sealing agent
water
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JP2009110354A
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Japanese (ja)
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JP2010260885A (en
JP5542366B2 (en
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Priority to JP2009110354A priority Critical patent/JP5542366B2/en
Priority claimed from JP2009110354A external-priority patent/JP5542366B2/en
Publication of JP2010260885A publication Critical patent/JP2010260885A/en
Publication of JP2010260885A5 publication Critical patent/JP2010260885A5/ja
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Publication of JP5542366B2 publication Critical patent/JP5542366B2/en
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Description

<評価>
1.パンクシーリング剤中の酸素濃度
パンクシーリング剤をステンレス容器に充填してから60分後に、ステンレス容器内のパンクシーリング剤中の酸素濃度を、島津製作所社製、溶存酸素計DO142を用いて測定した。下記評価基準により評価した。なお、許容範囲は○と◎である。
−評価基準−
◎:パンクシーリング剤中の酸素濃度が2g/L未満
○:パンクシーリング剤中の酸素濃度が2g/L以上4g/L未満
△:パンクシーリング剤中の酸素濃度が4g/L以上5g/L未満
×:パンクシーリング剤中の酸素濃度が5g/L以上
<Evaluation>
1. Oxygen concentration in puncture sealant 60 minutes after filling the puncture sealant into the stainless steel container, the oxygen concentration in the puncture sealant in the stainless steel container was measured using a dissolved oxygen meter DO142 manufactured by Shimadzu Corporation. Evaluation was performed according to the following evaluation criteria. The allowable ranges are ○ and ◎.
-Evaluation criteria-
◎: punk oxygen concentration in the sealing agent is less than 2 m g / L ○: puncture sealant oxygen concentration is less than 4 m g / L or more 2 m g / L of △: oxygen concentration in the puncture sealing agent 4 m g / L or more 5 m g / L less ×: oxygen concentration in the puncture sealing agent 5 m g / L or more

Claims (7)

少なくとも、ゴムラテックスと、水と、不凍液と、を混合する混合工程を有し、該混合工程中に超音波照射を行うパンクシーリング剤の製造方法。   The manufacturing method of the puncture sealing agent which has a mixing process which mixes rubber latex, water, and an antifreeze at least, and performs ultrasonic irradiation in this mixing process. 前記混合工程後に、濾過を行う濾過工程を有し、該濾過工程中に超音波照射を行う請求項1に記載のパンクシーリング剤の製造方法。   The method for producing a puncture sealing agent according to claim 1, further comprising a filtration step of performing filtration after the mixing step, and performing ultrasonic irradiation during the filtration step. 前記混合工程が、
ゴムラテックスと水とを混合する第1の混合工程と、
不凍液と粘着剤とを混合する第2の混合工程と、
前記第1の混合工程を経た混合液と前記第2の混合工程を経た混合液とを混合する第3の混合工程とを含む請求項1又は請求項2に記載のパンクシーリング剤の製造方法。
The mixing step is
A first mixing step of mixing rubber latex and water;
A second mixing step of mixing the antifreeze and the adhesive;
The manufacturing method of the puncture sealing agent of Claim 1 or Claim 2 including the 3rd mixing process which mixes the liquid mixture which passed through the said 1st mixing process, and the liquid mixture which passed through the said 2nd mixing process.
前記混合工程が、ゴムラテックスと粘着剤と水とを混合した後、不凍液を混合する混合工程を含む請求項1又は請求項2に記載のパンクシーリング剤の製造方法。   The method for producing a puncture sealing agent according to claim 1 or 2, wherein the mixing step includes a mixing step of mixing an antifreeze after mixing a rubber latex, an adhesive, and water. 前記混合工程が、不凍液と水とを混合して混合液を調製し、この混合液に、ゴムラテックスと粘着剤との混合液を混合する混合工程を含む請求項1又は請求項2に記載のパンクシーリング剤の製造方法。   3. The mixing process according to claim 1, wherein the mixing step includes a mixing step in which an antifreeze solution and water are mixed to prepare a mixed solution, and a mixed solution of rubber latex and an adhesive is mixed with the mixed solution. A method for producing a puncture sealant. 前記ゴムラテックスが、SBRラテックス、NBRラテックス、MBRラテックス、BRラテックス、カルボキシル変性NBRラテックス、及びカルボキシル変性SBRラテックスからなる群より選択される少なくとも1種である請求項1〜請求項5のいずれか1項に記載のパンクシーリング剤の製造方法。   The rubber latex is at least one selected from the group consisting of SBR latex, NBR latex, MBR latex, BR latex, carboxyl-modified NBR latex, and carboxyl-modified SBR latex. The manufacturing method of the puncture sealing agent as described in a term. 少なくとも、ゴムラテックスと、水と、不凍液と、を含有し、溶存酸素濃度が4mg/L未満であるパンクシーリング剤。A puncture sealant containing at least rubber latex, water, and antifreeze, and having a dissolved oxygen concentration of less than 4 mg / L.
JP2009110354A 2009-04-30 2009-04-30 Method for producing puncture sealant Expired - Fee Related JP5542366B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009110354A JP5542366B2 (en) 2009-04-30 2009-04-30 Method for producing puncture sealant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2009110354A JP5542366B2 (en) 2009-04-30 2009-04-30 Method for producing puncture sealant

Publications (3)

Publication Number Publication Date
JP2010260885A JP2010260885A (en) 2010-11-18
JP2010260885A5 true JP2010260885A5 (en) 2012-05-17
JP5542366B2 JP5542366B2 (en) 2014-07-09

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009110354A Expired - Fee Related JP5542366B2 (en) 2009-04-30 2009-04-30 Method for producing puncture sealant

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JP (1) JP5542366B2 (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008069253A (en) * 2006-09-13 2008-03-27 Bridgestone Corp Manufacturing method of puncture-sealing agent
EP2157150B1 (en) * 2007-05-10 2018-08-29 Bridgestone Corporation Puncture sealant
CA2701477C (en) * 2007-10-09 2016-09-27 Trydel Research Pty. Ltd. Improved sealing composition

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