JP5118150B2 - くし形共重合体を含む重合体混合物 - Google Patents
くし形共重合体を含む重合体混合物 Download PDFInfo
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- JP5118150B2 JP5118150B2 JP2009543388A JP2009543388A JP5118150B2 JP 5118150 B2 JP5118150 B2 JP 5118150B2 JP 2009543388 A JP2009543388 A JP 2009543388A JP 2009543388 A JP2009543388 A JP 2009543388A JP 5118150 B2 JP5118150 B2 JP 5118150B2
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- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
- 125000005462 imide group Chemical group 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical class O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002979 perylenes Chemical class 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 230000000485 pigmenting effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
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- C08F212/02—Monomers containing only one unsaturated aliphatic radical
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Description
I.
a)X1がNHを表す以下の構造単位I〜IVを含む共重合体の少なくとも1つのブロック、
および/または
b)X1がOを表す以下の構造単位I、IIおよびIVを含む共重合体の少なくとも1つのブロック
および/または
c)X1がNHまたはOを表す以下の構造単位I〜IVを含む共重合体の少なくとも1つのブロック
および/または
d)構造単位Iと、構造単位II〜IVとは異なる少なくとも1種のエチレン不飽和単量体の重合単位とを含む共重合体の少なくとも1つのブロック
を含む少なくとも1種のくし形共重合体であって、
ブロックd)が、前記ブロックa)〜c)のうちの1つと組み合わさるだけでブロック共重合体を形成し、
構造単位I〜IVが、以下を表し、
RがH、ハロゲン、好ましくは塩素、ニトロ基、炭素原子数1〜15のアルキル基、または炭素原子数6〜18のアリール基を表し、
R1が、炭素原子数1〜24のアルキレン基または炭素原子数6〜18の置換もしくは無置換アリーレン基を表し、
R2がHおよび/またはアルキル基を表し、
zが3〜70の整数を表し、
X1がNHおよび/またはOを表し、
R3が、モノ不飽和またはポリ不飽和であってよい場合により置換された炭素原子数1〜30のアルキル基、場合により置換された炭素原子数6〜18のアリール基、場合により置換された炭素原子数4〜10のシクロアルキル基を表し、
構造単位IVの遊離型(free)カルボキシル基が、アルカリ金属塩、アルカリ土類金属塩またはアンモニウム塩の形で存在することができるくし形共重合体と、
II.構造単位Iおよび構造単位IVに基づく少なくとも1種の共重合体であって、構造単位IVのカルボキシル基が、少なくとも部分的にはアルカリ土類金属塩、アンモニウム塩またはアルカリ金属塩の形で存在する共重合体と
を含む。
RがHであり、
R1が炭素原子数1〜6のアルキレン基であり、
R2がHおよび/またはCH3であり、構造単位IIおよび構造単位IIIにおけるエチレンオキシド単位対プロピレンオキシド単位のモル比が合計で0:100から100:0であり、
R3が炭素原子数1〜8のアルキル基または場合により置換された炭素原子数6のアリール基であり、
X1がNHおよび/またはOであり、
Zが5〜60の整数である。
RがHであり、
R1がエチレン、プロピレンおよび/またはイソプロピレン残基(residue)であり、
R2がHまたはCH3残基であり、エチレンオキシド単位対プロピレンオキシド単位のモル比が合計で70:30〜30:70であり、
R3がCH3またはC2H9残基であり、
zが27〜50の整数であり、
R1がNHおよび/またはOを表す場合、特に好ましい。
a1)好ましくは反応温度≧150℃で、第一級アミノ末端基を有する少なくとも1種のポリアルキレンオキシドモノアミンを用いて変換させることによって、かつ必要であれば、反応温度<100℃でさらに変換させることによって、
または
a2)好ましくは反応温度≧150℃で、第一級アミノ末端基を有する少なくとも1種のポリアルキレンオキシドモノアミンと、少なくとも1種のモノヒドロキシ末端ポリアルキレンオキシドの混合物を用いて変換させることによって、かつ必要であれば、反応温度<100℃でさらに変換させることによって、
または
a3)好ましくはたとえばスルホン酸など通常のエステル化触媒の存在下、少なくとも1種のモノヒドロキシ末端ポリアルキレンオキシドを用いて変換させることによって、
または
ABブロック共重合体構造を有する少なくとも1種の共重合体を、a1)、a2)もしくはa3)を用いて変換させることによって得られる。このABブロック共重合体構造のAブロックは、場合により置換されたスチレン単位と、(メタ)アクリレートおよびマレイン酸ジアルキルを含む群から選択される少なくとも1種の共重合エチレン不飽和単量体とを含み、このABブロック共重合体構造のBブロックは、場合により置換されたスチレン単位と、共重合無水マレイン酸単位とを含む。
・たとえばPolym.Int.2000,49,993、Aust.J.Chem 2005,58,379、J.Polym.Sci.Part A:Polym.Chem.2005,43,5347、米国特許第6291620号、WO98/01478号、WO98/58974号およびWO99/31144号に開示されているような、特定の連鎖移動剤を使用する場合にはMADIXおよび付加開裂連鎖移動とも呼ばれるが、ここではRAFTとだけ称される可逆的付加開裂連鎖移動プロセス(reversible addition fragmentation chain transfer process)、または
・たとえばChem.Rev.2001,101,3661に開示されているような、連鎖移動剤としてニトロキシル化合物を用いる制御された重合(NMP)。
有利には、サーマルインクジェットプロセスやバブルジェット(登録商標)プロセスなどの「ノンインパクト」印刷プロセス用インクの製造において、本発明による重合体混合物を使用することもできる。これらのインクは、たとえば、水性インク調合物でよい。
a)ポリエーテルMSA半エステル
Pluriol A 750Eの375g、Polyglycol B01/20の42g、無水マレイン酸の55gを、ドデシルベンゾルスルホン酸2gの存在下135℃で3時間反応させる。
Pluriol P600の10.5g、2,4−ジフェニル−4−メチル−1−ペンテンの3.9gを、160℃まで加熱する。その後、スチレン8.7gと、マレイン酸ジブチル4.2gと、アクリル酸ベンジルメチル8.7gと、Trigonox C0.2gとを、2時間かけて添加する。その後1時間の反応時間の後、温度を135℃まで下げ、a)に従って得られたポリエーテル−MSA半エステル混合物170gを添加する。その後スチレン34gとTrigonox C1.7gとを、1時間かけて何回かに分けて添加する。その後4時間の反応時間の後、この反応混合物を室温まで冷却する。
酢酸ブチル60gに溶解させたSMA 2000合成樹脂20gを、116gのJeffamine M 2070と160℃で4時間反応させる。この間に酢酸ブチルを蒸留する。
100gのくし形共重合体1を水100g中で乳化し、N,N−ジエチルアミノエタノールを用いてpH9に調整する。その後この混合物を1時間で95℃まで加熱し、固形分が40wt%になるまで調整する。
SMA 2000合成樹脂5gと、p−トルオールスルホン酸0.1gとを、水100g中で乳化し、95℃で8時間反応させる。その後100gのくし形共重合体1を添加し、N,N−ジエチルアミノエタノールを用いてpH9に調整する。水を添加することによって、固形分40wt%を調整する。
100gのくし形共重合体2を、水150gに溶解させる。
SMA 2000合成樹脂5gと、p−トルオールスルホン酸0.1gとを、水100g中で乳化し、95℃で8時間反応させる。その後56gのくし形共重合体2を添加し、塩化のために18gのJeffamine M2070と混合する。水を添加することによって、固形分40wt%を調整する。
Pluriol A 750E ポリエチレングリコールモノメチルエーテル、ヒドロキシル価75g KOH/g、製造業者BASF
Polyglycol B01/20 ポリプロピレングリコールモノブチルエーテル、ヒドロキシル価80g KOH/g、製造業者Clariant
Pluriol P600 ポリプロピレングリコール、ヒドロキシル価195g KOH/g、製造業者BASF
Trigonox C tert−ブチルペルオキソベンゾエート、製造業者Akzo Nobel
SMA2000合成樹脂 スチレン−無水マレイン酸共重合体、製造業者Cray Valley
Jeffamin M2070 アミン末端EO/POポリエーテル、製造業者Huntsman
下塗り(base coat)Sikkens Autowave MM 無着色自動車修理用ベース塗料、水性アクリレート分散液、製造業者Akzo Nobel
Claims (16)
- I.
a)X1がNHを表す以下の構造単位I〜IVを含む共重合体の少なくとも1つのブロック、
および/または
b)X1がOを表す以下の構造単位I、IIおよびIVを含む共重合体の少なくとも1つのブロック
および/または
c)X1がNHまたはOを表す以下の構造単位I〜IVを含む共重合体の少なくとも1つのブロック
および/または
d)構造単位Iと、構造単位II〜IVとは異なる少なくとも1種のエチレン不飽和単量体の重合単位とを含む共重合体の少なくとも1つのブロック
を含む少なくとも1種のくし形共重合体であって、
前記ブロックd)が含まれる場合には、前記ブロックa)〜c)のうちの1つも含まれ、前記ブロックa)〜c)のうちの1つと組み合わさるだけでブロック共重合体を形成し、
構造単位I〜IVが、以下を表し、
RがH、ハロゲン、ニトロ基、炭素原子数1〜15のアルキル基、または炭素原子数6〜18のアリール基を表し、
R1が、炭素原子数1〜24のアルキレン基または炭素原子数6〜18の置換もしくは無置換アリーレン基を表し、
R2がHおよび/またはアルキル基を表し、
zが3〜70の整数を表し、
X1がNHおよび/またはOを表し、
R3が、場合により置換された炭素原子数1〜30のアルキル基を表すか、モノ不飽和またはポリ不飽和である、場合により置換された炭素原子数1〜30のアルケニル基を表すか、場合により置換された炭素原子数6〜18のアリール基を表すか、または場合により置換された炭素原子数4〜10のシクロアルキル基を表し、
構造単位IVの遊離型カルボキシル基が、アルカリ金属塩、アルカリ土類金属塩またはアンモニウム塩の形で存在することができる、
少なくとも1種のくし形共重合体と、
II.構造単位Iおよび構造単位IVに基づく少なくとも1種の共重合体であって、構造単位IVのカルボキシル基が、少なくとも部分的にはアルカリ土類金属塩、アンモニウム塩またはアルカリ金属塩の形で存在する共重合体と
を含む重合体混合物。 - 構造単位I〜IVにおいて、
RがHであり、
R1が炭素原子数1〜6のアルキレン基であり、
R2がHおよび/またはCH3であり、
構造単位IIおよび構造単位IIIにおけるエチレンオキシド単位対プロピレンオキシド単位のモル比が合計で0:100から100:0であり、
R3が、炭素原子数1〜8のアルキル基または場合により置換された炭素原子数6のアリール基であり、
X1がNHおよび/またはOであり、
zが5〜60の整数であることを特徴とする請求項1に記載の重合体混合物。 - 構造単位I〜IVにおいて、
RがHであり、
R1がエチレン、プロピレンおよび/またはイソプロピレン残基であり、
R2がHまたはCH3残基であり、
構造単位IIおよび構造単位IIIにおけるエチレンオキシド単位対プロピレンオキシド単位のモル比が合計で70:30から30:70であり、
R3がCH3またはC4H9残基であり、
zが25〜50の整数であり、
X1がNHおよび/またはOであることを特徴とする請求項1に記載の重合体混合物。 - 前記エチレン不飽和単量体が、(メタ)アクリル酸誘導体およびマレイン酸ジエステルを含む群から選択される少なくとも1種の単量体であることを特徴とする請求項1〜3のいずれかに記載の重合体混合物。
- くし形共重合体I対共重合体IIの重量比が、50:50から95:5の範囲内にあることを特徴とする請求項1〜4のいずれかに記載の重合体混合物。
- 場合により置換されたスチレン単位および無水マレイン酸単位から、無水物基の加水分解および塩化によって共重合体IIを得ることができることを特徴とする請求項1〜5のいずれかに記載の重合体混合物。
- アミノ基を有する少なくとも1種の化合物により、遊離型カルボキシル基の塩化が生じることを特徴とする請求項1〜6のいずれかに記載の重合体混合物。
- くし形共重合体Iを共重合体IIと混合することによって得られる請求項1〜7のいずれかに記載の重合体混合物。
- 湿潤兼分散剤としての請求項1〜8のいずれかに記載の重合体混合物の使用。
- 顔料および/または充填剤に対する請求項9に記載の使用。
- 顔料コンセントレートまたはペーストの製造および/または加工するための請求項9または請求項10に記載の使用。
- 塗料、印刷インク、インクジェットプロセス用のインク、コーティング、革および/または織物染料、セラミックス、または化粧品の製造および/または加工のための請求項9〜11のいずれかに記載の使用。
- 補助剤として結合剤も使用されることを特徴とする請求項9〜12のいずれかに記載の使用。
- 湿潤兼分散剤としての請求項1〜8のいずれかに記載の重合体混合物と、少なくとも1種の顔料と、必要に応じて水性媒体と、必要に応じて少なくとも1種の結合剤とを含有する塗料またはペースト。
- 請求項1〜8のいずれかに記載の重合体混合物によって表面が改質された顔料。
- 前記(メタ)アクリル酸誘導体が、(メタ)アクリル酸アルキルまたは(メタ)アクリル酸アリールであり、前記マレイン酸ジエステルが、マレイン酸ジアルキルである請求項4に記載の重合体混合物。
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- 2007-12-21 EP EP07857048A patent/EP2106412B1/de active Active
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Publication number | Publication date |
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CA2671827C (en) | 2015-12-01 |
CN101600744A (zh) | 2009-12-09 |
US20100029834A1 (en) | 2010-02-04 |
WO2008080581A1 (de) | 2008-07-10 |
JP2010514864A (ja) | 2010-05-06 |
ATE472569T1 (de) | 2010-07-15 |
KR101459352B1 (ko) | 2014-11-07 |
DE502007004292D1 (de) | 2010-08-12 |
EP2106412A1 (de) | 2009-10-07 |
TWI417305B (zh) | 2013-12-01 |
TW200842131A (en) | 2008-11-01 |
KR20090104078A (ko) | 2009-10-05 |
US9079996B2 (en) | 2015-07-14 |
EP2106412B1 (de) | 2010-06-30 |
ES2345738T3 (es) | 2010-09-30 |
CA2671827A1 (en) | 2008-07-10 |
DE102006062440A1 (de) | 2008-07-03 |
CN101600744B (zh) | 2013-04-24 |
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