JP2004250655A5 - - Google Patents

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JP2004250655A5
JP2004250655A5 JP2003129891A JP2003129891A JP2004250655A5 JP 2004250655 A5 JP2004250655 A5 JP 2004250655A5 JP 2003129891 A JP2003129891 A JP 2003129891A JP 2003129891 A JP2003129891 A JP 2003129891A JP 2004250655 A5 JP2004250655 A5 JP 2004250655A5
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styrene
resin particles
weight
polymerization
average molecular
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JP2003129891A
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JP3926289B2 (en
JP2004250655A (en
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Publication of JP2004250655A5 publication Critical patent/JP2004250655A5/ja
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【特許請求の範囲】
【請求項1】 粒子の表面から中心に向かって5等分した表面から1/5までを形成する表面部分の重量平均分子量が、前記中心から前記表面に向かって中心から1/5までを形成する中心部分の重量平均分子量より高く、
前記表面部分のゲルパーミエーションクロマトグラフ法のチャートが二山又はショルダーを有することを特徴とするスチレン系発泡性樹脂粒子。
【請求項2】 前記中心部分の重量平均分子量が200,000〜300,000の範囲であり、
前記表面部分の重量平均分子量が300,000〜450,000の範囲であり、
前記表面部分の重量平均分子量が、前記中心部分の重量平均分子量に対して、1.2倍以上大きいことを特徴とする請求項1記載のスチレン系発泡性樹脂粒子。
【請求項3】 樹脂粒子中心から表面に向かって30〜60重量%までを形成する樹脂部分の重量平均分子量が200,000〜300,000の範囲であり、
表面から中心に向かって60〜30重量%までを形成する樹脂部分の重量平均分子量が300,000〜450,000の範囲であること、
および、中心部分30〜60重量%までの重量平均分子量に対して、表面部分60〜30重量%までの重量平均分子量が、1.2〜2.2倍大きくなることを特徴とするスチレン系発泡性樹脂粒子。
【請求項4】 粒子の表面から中心に向かって5等分した表面から1/5までを形成する表面部分の、GPC/MALLS法により測定したlog(R.M.S半径)とlog(MW)との相関式の傾きが、0.53以下であることを特徴とするスチレン系発泡性樹脂粒子。
【請求項5】 スチレン系単量体の懸濁重合において、
重合後期のとき、反応槽内の酸素濃度を低く保ちつつ、スチレン系単量体を添加し、重合途中にあるスチレン樹脂粒子に吸着させて重合反応を進め、
重合反応の完了前または重合反応の完了後に、発泡剤を含浸するスチレン系発泡性樹脂粒子の製造方法。
【請求項6】 スチレン系単量体の懸濁重合において、
重合率が60%以上のとき、反応槽内の酸素濃度を7体積%以下に保ちつつ、スチレン系単量体を添加し、重合途中にあるスチレン樹脂粒子に吸着させて重合反応を進め、
重合反応の完了前または重合反応の完了後に、発泡剤を含浸することを特徴とするスチレン系発泡性樹脂粒子の製造方法。
【請求項7】 前記重合率が60%以上97%未満で、前記反応槽内の酸素濃度を5体積%以下に保つことを特徴とする請求項5又は6記載のスチレン系発泡性樹脂粒子の製造方法。
【請求項8】 前記添加するスチレン系単量体が、前記スチレン系発泡性樹脂粒子の5重量%〜30重量%であることを特徴とする請求項5〜7のいずれか一項記載のスチレン系発泡性樹脂粒子の製造方法。
【請求項9】 前記スチレン系単量体の懸濁重合において、水分散液の水素イオン濃度が8〜10で重合が開始し、
重合率20%〜50%で、少なくとも1回以上、難溶性無機塩を加えることを特徴とする請求項5〜8のいずれか一項記載のスチレン系発泡性樹脂粒子の製造方法。
【請求項10】 再生ビーズを核として用い、これにスチレン系単量体を添加する請求項5〜9のいずれか一項記載のスチレン系発泡性樹脂粒子の製造方法。
【請求項11】 請求項5〜10のいずれか一項記載の製造方法により得られることを特徴とするスチレン系発泡性樹脂粒子。
【請求項12】 請求項1、請求項2、請求項3、請求項4又は請求項11記載のスチレン系発泡性樹脂粒子を発泡させて得られることを特徴とするスチレン系発泡ビーズ。
【請求項13】 請求項12記載のスチレン系発泡ビーズを成形させて得られることを特徴とするスチレン系発泡成形品。
[Claims]
    1. The weight-average molecular weight of a surface portion forming 1/5 from the surface divided into 5 equal parts from the surface of the particle toward the center, and forming 1/5 from the center toward the surface from the center. Higher than the weight average molecular weight of the central part,
  Styrene-based foamable resin particles characterized in that the chart of the surface portion by gel permeation chromatography has two peaks or shoulders.
    2. The weight average molecular weight of the central portion is in the range of 200,000 to 300,000,
  The weight average molecular weight of the surface portion is in the range of 300,000 to 450,000;
  The styrene-based expandable resin particles according to claim 1, wherein the weight average molecular weight of the surface portion is 1.2 times or more larger than the weight average molecular weight of the central portion.
    3. The resin part forming from 30 to 60% by weight from the center of the resin particle toward the surface has a weight average molecular weight in the range of 200,000 to 300,000,
  The weight-average molecular weight of the resin portion forming from 60 to 30% by weight from the surface toward the center is in the range of 300,000 to 450,000;
  And a styrene-based foam characterized in that the weight average molecular weight of the surface portion of 60 to 30% by weight is 1.2 to 2.2 times larger than the weight average molecular weight of the central portion of 30 to 60% by weight. Resin particles.
    4. The log (RMS radius) and log (MW) measured by GPC / MALLS method for the surface portion forming 1/5 from the surface divided into five equal parts from the surface of the particle toward the center. The styrene-based expandable resin particles have a slope of 0.53 or less.
    5. The suspension polymerization of a styrene monomer,
During the late stage of polymerization, while keeping the oxygen concentration in the reaction tank low, a styrene monomer is added, and the styrene resin particles are adsorbed on the styrene resin particles in the course of polymerization, and the polymerization reaction proceeds.
  A method for producing styrene-based expandable resin particles in which a foaming agent is impregnated before or after completion of the polymerization reaction.
    6. The suspension polymerization of a styrene monomer,
  When the polymerization rate is 60% or more, while maintaining the oxygen concentration in the reaction vessel at 7% by volume or less, a styrene monomer is added, and the styrene monomer is adsorbed on the styrene resin particles in the course of polymerization to advance the polymerization reaction.
  A method for producing styrenic foamable resin particles, comprising impregnating a foaming agent before or after completion of the polymerization reaction.
    7. The styrenic foamable resin particles according to claim 5, wherein the polymerization rate is 60% or more and less than 97%, and the oxygen concentration in the reaction vessel is kept at 5% by volume or less. Production method.
    8. The styrene according to claim 5, wherein the styrene-based monomer to be added is 5% by weight to 30% by weight of the styrene-based expandable resin particles. Method for producing foamable resin particles.
    9. In the suspension polymerization of the styrene-based monomer, polymerization starts when the hydrogen ion concentration of the aqueous dispersion is 8 to 10,
  The method for producing styrene-based expandable resin particles according to any one of claims 5 to 8, wherein the poorly soluble inorganic salt is added at least once or more at a polymerization rate of 20% to 50%.
    10.   The method for producing styrene-based expandable resin particles according to any one of claims 5 to 9, wherein the recycled beads are used as nuclei, and a styrene-based monomer is added to the nuclei.
    11.   Any one of claims 5 to 10A styrene-based expandable resin particle obtained by the production method described above.
    12.  Claim 1, Claim 2, Claim 3, Claim 4, orClaim 11Styrene-based expanded beads obtained by expanding the styrene-based expandable resin particles.
    Claim 13   Claim 12A styrene foam molded article obtained by molding the styrene foam beads.

JP2003129891A 2002-05-08 2003-05-08 Styrenic expandable resin particles, expanded beads and expanded molded products Expired - Fee Related JP3926289B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2003129891A JP3926289B2 (en) 2002-05-08 2003-05-08 Styrenic expandable resin particles, expanded beads and expanded molded products

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2002132623 2002-05-08
JP2002242015 2002-08-22
JP2002381173 2002-12-27
JP2003129891A JP3926289B2 (en) 2002-05-08 2003-05-08 Styrenic expandable resin particles, expanded beads and expanded molded products

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2006275936A Division JP2007002265A (en) 2002-05-08 2006-10-10 Expandable styrene resin particles, expandable beads, and foamed article

Publications (3)

Publication Number Publication Date
JP2004250655A JP2004250655A (en) 2004-09-09
JP2004250655A5 true JP2004250655A5 (en) 2006-05-11
JP3926289B2 JP3926289B2 (en) 2007-06-06

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JP2003129891A Expired - Fee Related JP3926289B2 (en) 2002-05-08 2003-05-08 Styrenic expandable resin particles, expanded beads and expanded molded products

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Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4653405B2 (en) * 2004-03-08 2011-03-16 積水化成品工業株式会社 Method for producing expandable styrene resin particles, expandable styrene resin particles, pre-expanded styrene resin particles, and styrene resin foam molded article
JP2006160905A (en) * 2004-12-08 2006-06-22 Hitachi Chem Co Ltd Reclaimed foamable sytrenic resin particle, method for producing the same, reclaimed styrenic foamed bead and reclaimed foamed styrenic resin molded article
JP2006316240A (en) * 2005-04-11 2006-11-24 Hitachi Chem Co Ltd Foamed styrenic block molded product
JP2006307016A (en) * 2005-04-28 2006-11-09 Hitachi Chem Co Ltd Method for producing recycled foaming styrenic resin particle
JP2006316176A (en) * 2005-05-13 2006-11-24 Hitachi Chem Co Ltd Method for producing regenerated foaming styrene resin particle
JP4891586B2 (en) * 2005-09-28 2012-03-07 積水化成品工業株式会社 Expandable thermoplastic resin particles and process for producing the same, thermoplastic resin pre-expanded particles, and foam molded article
JP2007131826A (en) * 2005-10-13 2007-05-31 Hitachi Chem Co Ltd Pre-expanded resin particle, formed product of expanded resin and manufacturing method thereof
JP2007270120A (en) * 2005-11-15 2007-10-18 Daiden Co Ltd Extrusion molded form and method for producing the same, and optical fiber cable
JP5732358B2 (en) * 2011-09-12 2015-06-10 積水化成品工業株式会社 Polystyrene-based resin particles, expandable resin particles, expanded particles, expanded molded articles, and methods for producing them

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