CN103476865A - 阻燃的热塑性模制组合物 - Google Patents
阻燃的热塑性模制组合物 Download PDFInfo
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- CN103476865A CN103476865A CN201280018664XA CN201280018664A CN103476865A CN 103476865 A CN103476865 A CN 103476865A CN 201280018664X A CN201280018664X A CN 201280018664XA CN 201280018664 A CN201280018664 A CN 201280018664A CN 103476865 A CN103476865 A CN 103476865A
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Abstract
本发明涉及一种热塑性模制组合物,其不含卤素和稀土金属并且包含:A)40至60重量%的聚对苯二甲酸亚烷基酯;B)0.01至10重量%的选自下列的聚烯烃:b1)聚乙烯、b2)聚丙烯、b3)聚丙烯共聚物,以及它们的混合物;C)10至30重量%的选自下列的阻燃剂:c1)含氮化合物、c2)含磷化合物,以及它们的混合物;D)0.01至60重量%的增强剂;E)0至50重量%的其它添加剂,其中所有重量比的总和为100重量%,基于热塑性模制组合物计。本发明还涉及所述热塑性模制组合物用于制备纤维、箔或模制品的用途,以及涉及含有本发明的热塑性模制组合物的纤维、箔或模制品。本发明还涉及所述热塑性模制组合物作为涂覆材料的用途。
Description
本发明涉及热塑性模制组合物,其不含卤素和稀土金属且包含
A)40至60重量%的聚对苯二甲酸亚烷基酯
B)0.01至10重量%的选自下列的聚烯烃
b1)聚乙烯
b2)聚丙烯
b3)聚丙烯共聚物
以及它们的混合物;
C)10至30重量%的选自下列的阻燃剂
c1)含氮化合物
c2)含磷化合物
以及它们的混合物;
D)0.01至60重量%的增强剂;
E)0至50重量%的其它添加剂
其中所有重量比的总和为100重量%,基于热塑性模制组合物计。
本发明还涉及本发明的热塑性模制组合物用于制备纤维、箔或模制品的用途,以及涉及包含本发明热塑性模制组合物的纤维、箔或模制品。本发明还涉及所述热塑性模制组合物作为涂覆材料的用途。
优选的实施方案可见于权利要求书和说明书中。优选实施方案的组合也在本发明的范围内。
对阻燃性模制组合物需求的兴趣正在增长,并且对不含可对环境和人类有害的添加剂的组合物有着特别的需求。同时,所述模制组合物旨在符合严格的技术规范。
KR1020070117410的说明书公开了包含聚对苯二甲酸亚烷基酯和聚烯烃的模制组合物。碱式盐被用作阻燃剂。
文献JP11335534、JP11335534、JP11335534和JP11335534也公开了包含聚对苯二甲酸亚烷基酯和聚烯烃和模制组合物。其中公开的模制组合物包含红磷作为阻燃剂。
CN101434727公开了包含不含卤素的阻燃剂、包含聚对苯二甲酸亚烷基酯和聚烯烃的模制组合物。
CN101445650的说明书公开了包含聚对苯二甲酸亚烷基酯和聚烯烃的模制组合物。所述模制组合物包含稀土金属盐。该稀土金属盐作为成核剂以较少的量添加。
本发明的一个目的是开发一种具有良好的可加工型以及同时表现出阻燃效果的模制组合物。本发明的另一个目的是提供一种具有高耐漏电起痕性的模制组合物。所述模制组合物还应当具有最小的内着色。
然而,所述模制组合物应当不含卤素,特别是不含氯和不含溴。所述模制组合物还应当即不包含红磷,也不包含稀土金属盐。
该目的通过使用前述的热塑性模制组合物而实现。
本发明的热塑性模制组合物不含卤素。本文中对不含卤素的定义相当于“International Electrotechnical Commission”(IEC61249-2-21)和“Japan Printed Circuit Association”(JPCA-ES-01-1999)中的定义,其中将不含卤素的材料定义为绝大部分(very substantially)不含氯和溴的材料。
所述热塑性模制组合物还不包含稀土金属,例如镧或铈。
本发明的热塑性模制组合物特别地包含不含卤素的阻燃剂。
本发明的热塑性模制组合物的组分A)为聚对苯二甲酸亚烷基酯。该术语还涵盖了不同结构和/或链长的聚对苯二甲酸亚烷基酯的混合物。
为了本发明的目的,术语聚对苯二甲酸亚烷基酯并不限于包含对苯二甲酸酯的化合物。所述聚对苯二甲酸亚烷基酯可因此还包含至少一种不同于对苯二甲酸的酸。
所述酸可衍生自如下结构:所述结构的主链上具有衍生自芳族二元羧酸的芳环。所述芳环可为未取代或取代的环。可用的取代基为特别是C1-至C4-烷基,例如甲基、乙基、异丙基、正丙基和正丁基、异丁基以及叔丁基或氟。
优选的二元羧酸为取代的或特别是未取代的2,6-萘二酸、对苯二甲酸和间苯二甲酸,或其混合物。其中,优选对苯二甲酸或间苯二甲酸或其混合物。
聚对苯二甲酸亚烷基酯除衍生自合适的二元羧酸的基团外还包含脂族烃基团,其中所述脂族烃基团衍生自合适的烷二醇。所述烷二醇可为支链的或无支链的(即直链的)烷二醇。支链的聚对苯二甲酸亚烷基酯包含支链的烃基团,而直链的聚对苯二甲酸亚烷基酯则包含无支链的烃基团。本发明的热塑性组合物优选使用直链的聚对苯二甲酸亚烷基酯。
在烷二醇中,优选具有2至6个碳原子的二醇,特别是1,2-乙二醇、1,3-丙二醇、1,4-丁二醇、1,6-己二醇、1,4-己二醇、1,4-环己二醇、1,4-环己烷二甲醇或新戊二醇或所述二醇的任何混合物。
在本发明的一个优选实施方案中,组分A可包含聚对苯二甲酸亚乙酯、聚对苯二甲酸1,3-亚丙酯、聚对苯二甲酸1,4-亚丁酯、聚萘二甲酸亚乙酯、聚萘二甲酸1,4-亚丁酯、聚对苯二甲酸1,3-亚丙酯、聚(对苯二甲酸环己烷二甲醇酯)或其混合物,其中组分A包含5至20重量%的不同于对苯二甲酸的酸。
所述聚对苯二甲酸亚烷基酯通常具有0.4dL/g至2.0dL/g的特性粘度,所述特性粘度在苯酚/四氯化碳(1/1,体积比)中测量。所述聚对苯二甲酸亚烷基酯通常具有5000至130000g/mol(Mw)的平均摩尔量(在25℃下,氯仿/六氟异丙醇(5/95,体积比)中通过凝胶渗透色谱法以聚苯乙烯为标准品测量而测定)。
作为组分B),本发明的热塑性模制组合物包含:由包含乙烯和/或丙烯的重复单元构成的聚烯烃,其中不含极性官能团。其中本发明包含不同链长的所述聚烯烃的混合物。
极性官能团为所含单体单元内包含除碳和氢之外的原子的任何官能团。因此,本发明中使用的聚烯烃基本上由单体单元乙烯和/或丙烯组成,其中所排除的基团涵盖包含共聚单体和/或官能团的单团单元并且还涵盖不饱和基团。因此,组分B)由不饱和脂族重复单元构成,所述重复单元由碳和氢构成。
然而,组分B)的聚烯烃可包含常规的支化点,以及少量的,特别是至多2重量%的由碳和氢构成的其它单体单元。因此,组分B)的聚烯烃可包含少量的(即特别是至多2重量%,基于聚烯烃计)的其它单体单元,例如衍生自1-丁烯、1-戊烯、1-己烯、1-庚烯或1-辛烯或4-甲基-1-戊烯的单体单元。
因此,作为组分B),所述热塑性模制组合物包含至少一种基本上由选自乙烯和丙烯的重复单元组成的直链或支链的聚烯烃。
组分B)优选选自聚乙烯、聚丙烯和共聚聚丙烯以及它们的混合物。优选组分B)为聚丙烯和/或聚(丙烯-乙烯)。
为了本发明的目的,当使用术语聚乙烯时,其表示乙烯的均聚物。聚乙烯b1)还可为不同结构和/或链长的均聚物的混合物。
所用的聚乙烯b1)通常的熔体流动指数(MFR,在190℃,2.16kg下测量)为0.1g/10min至100g/10min,优选2g/10min至50g/10min。聚乙烯(b1)的摩尔量(Mw)通常为85000至900000g/mol,优选95000至750000g/mol(在130℃下以聚苯乙烯为标准品在三氯苯中通过高温GPC测定)。聚乙烯的密度为0.850g/cm3至0.925g/cm3,优选0.870g/cm3至0.925g/cm3(根据DIN EN ISO1183-1通过浸渍法测量)。
为了本发明的目的,当使用术语聚丙烯时,其表示丙烯的均聚物,并且其可具有支链,特别是直链的支链。聚丙烯b2)还可为不同结构和链长的均聚聚丙烯的混合物。
聚丙烯b2)通常的熔体流动指数(MFR,在230℃,2.16kg下测量)为0.1g/10min至100g/10min,优选2g/10min至50g/10min。聚丙烯)的摩尔量(Mw)通常为85000至900000g/mol,优选95000至750000g/mol(在135℃下以聚苯乙烯为标准品在三氯苯中通过高温GPC测定)。聚丙烯的密度为0.850g/cm3至0.925g/cm3,优选0.870g/cm3至0.925g/cm3(根据DIN EN ISO1183-1通过浸渍法测量)。
共聚聚丙烯b3)优选为无规共聚物或不同结构和/或链长的无规共聚物的混合物。
共聚物b3)特别是由丙烯和乙烯以及至多为2重量%的其它C3-C20烯烃构成,所述C3-C20烯烃包括1-丁烯、1-戊烯、1-己烯、甲基-1-丁烯、甲基-1-戊烯、1-辛烯、1-癸烯以及它们的混合物。
优选的共聚聚丙烯b3)为共聚(丙烯-乙烯),其由丙烯和乙烯制备。所述共聚(丙烯-乙烯)b3)中的丙烯含量可为75至98重量%,优选85-95重量%。所述共聚(丙烯-乙烯)中的乙烯含量可为2-25重量%,特别是5-15重量%。
所用的共聚聚丙烯b3)通常的熔体流动指数(MFR,在230℃,2.16kg下测量)为0.1g/10min至100g/10min,优选2g/10min至50g/10min。共聚聚丙烯的摩尔量(Mw)通常为85000至900000g/mol,优选95000至750000g/mol(在135℃下以聚苯乙烯为标准品在三氯苯中通过高温GPC测定)。共聚聚丙烯的密度为0.850g/cm3至0.925g/cm3,优选0.870g/cm3至0.925g/cm3(根据DIN EN ISO1183-1通过浸渍法测量)。
本发明所用的聚烯烃可通过聚合单体乙烯和丙烯中的至少一种而获得。所述聚合的方法是本领域技术人员已知的。
本发明的热塑性模制组合物还可包含阻燃剂C),其选自含氮化合物c1)、含磷化合物c2)及其混合物。
作为包含化合物c1),本发明的热塑性模制组合物可包含选自具有至少一个氮原子的含氮杂环的不含卤素的化合物。所述热塑性组合物还可包含具有至少一个氮原子的含氮杂环的混合物。
在所述阻燃剂中,优选适于本发明的为三聚氰胺氰脲酸盐。三聚氰胺氰脲酸盐为优选等摩尔的量的三聚氰胺(式(I))和氰脲酸或异氰脲酸(式(Ia)及(Ib))的反应产物。
三聚氰胺氰脲酸盐可通过例如在90至100℃下起始化合物水溶液的反应而获得。
其它合适的化合物(通常也称为盐或加合物)为三聚氰胺、三聚氰胺硼酸盐和三聚氰胺草酸盐。也可使用所述盐的混合物。然而,排除使用具有至少一个氮原子和稀土元素的含氮杂环的盐。
术语含氮阻燃剂还涵盖WO2002/96976中描述的含氮阻燃剂。
其中合适的化合物为磷酸二氢钙(melamine phosphate prim.)、磷酸二(三聚氰胺)(melamine phosphate sec.)以及焦磷酸二(三聚氰胺)(melamine pyrophosphate sec.)、三聚氰胺-新戊二醇硼酸盐(melamineneopentyl glycol borate)和聚合磷酸三聚氰胺(CAS No.56386-64-2)。
合适的胍盐为
为了本发明的目的,化合物的实例旨在包括苯并胍胺本身及其加合物或盐,以及氮上取代的衍生物以及它们的加合物或盐。
磷酸铵也是合适的。同样合适的是聚磷酸铵(NH4PO3)n,其中n为约200至1000,优选600至800,以及式II的三(羟乙基)异氰脲酸酯(THEIC)
式III的苯并胍胺化合物也是合适的。
其中R9和R10为具有1至10个碳原子的直链或支链烷基,优选为氢,并且所述化合物与磷酸、硼酸和/或焦磷酸的加合物是特别合适的。
还优选式IV的尿囊素化合物
其中R9和R10的定义为式III中所述的定义,还优选所述化合物与磷酸、硼酸和/或焦磷酸的盐,还优选式V的甘脲或所述化合物与上述酸的盐
其中R9的定义如式III所述。
可用于本发明的氰基胍(式VI)通过例如以下方法获得:氰氨化钙与碳酸的反应,由此所得的氨腈在pH为9至10下二聚以得到氰氨化钙。
特别合适的含氮化合物(c1)为选自具有至少1个氮原子的含氮杂环的化合物。
作为含磷化合物(c2),所述热塑性模制组合物可包含式(VII)的次磷酸盐或式(VIII)的二次磷酸和/或它们的聚合物。所述热塑性组合物还可包含含磷化合物(c2)的混合物。然而,不使用稀土金属元素作为阳离子。
在适用于本发明的大量含磷化合物中,仅可提及一些实例。
其中取代基的定义如下:
R11和R12为氢或直链或支链的C1-C6-烷基,优选C1-C4-烷基,例如甲基、乙基、正丙基、异丙基、正丁基、叔丁基、正戊基、苯基,其中至少一个基团R11或R12优选为氢或乙基并且特别是R11和R12为氢或乙基;
R13为直链或支链的C1-C10-亚烷基,例如亚甲基、亚乙基、亚正丙基、亚异丙基、亚正丁基、亚叔丁基、亚正戊基、亚正辛基、亚正十二烷基;
亚芳基,例如亚苯基、亚萘基;
烷基亚芳基,例如甲基亚苯基、乙基亚苯基、叔丁基亚苯基、
甲基亚萘基、乙基亚萘基、叔丁基亚萘基;
芳基亚烷基,例如苯基亚甲基、苯基亚乙基、苯基亚丙基、苯基亚丁基;
M 为碱土金属或碱金属、Al、Zn、Fe、Mg、Ca;
s 为1至3的整数;
z 为1和3的整数;和
x 为1或2。
特别优选的是式VII化合物,其中R11和R12为氢、甲基、乙基或异丁基,其中M优选为Ca、Zn、Mg或Al,极特别优选二乙基次膦酸铝和次膦酸铝。
可用的氧化态为+5的磷化合物特别是烷基和芳基取代的磷酸酯。所述磷酸酯的实例为苯基双十二烷基磷酸酯、苯基乙基磷酸氢酯、苯基双(3,5,5-三甲基己基)磷酸酯、乙基二苯基磷酸酯、2-乙基己基二甲苯基磷酸酯、二苯基磷酸氢酯、双(2-乙基己基)对甲苯基磷酸酯、三(甲苯基)磷酸酯、双(2-乙基己基)苯基磷酸酯、二(壬基)苯基磷酸酯、苯基甲基磷酸氢酯、双十二烷基对甲苯基磷酸酯、对甲苯基双(2,5,5-三甲基己基)磷酸酯和2-乙基己基二苯基磷酸酯。特别合适的磷化合物为其中每个基团均为芳氧基的磷化合物。极特别合适的化合物为三苯基磷酸酯和/或间苯二酚双(二苯基磷酸酯)及其通式X的环取代的衍生物(RDP):
其中所述基团的定义如下:
R18-R21为具有6至20个碳原子的芳基,优选苯基,所述芳基可被具有1至4个碳原子的烷基取代,优选甲基,
R22为二价的苯酚基团,优选为
和
n具有0.1至100、优选0.5至50、特别是0.8至10且极特别是1至5的平均值。
作为该制备方法的结果,目前可市购的RDP产品为由约85%的RDP(n=1)与约2.5%的三苯基磷酸酯以及约12.5%的低聚度通常小于10的低聚部分制成的混合物。
化合价为+0的磷不是适于本发明目的的化合物,因此不适于作为本发明的阻燃剂。因此,本发明的热塑性模制组合物不含红磷。
本发明的热塑性模制组合物包含纤维或粒状添加剂D)。还可使用不同添加剂的混合物作为添加剂D)。所述添加剂D)可例如包括玻璃纤维、碳纤维、芳族聚酰胺纤维、钛酸钾纤维、玻璃珠、无定形二氧化硅、硅酸钙、碳酸镁、高岭土、白垩、粉石英、云母、硫酸钡、长石、金属氢氧化物、金属氧化物、相似的矿物填料或陶瓷。也可使用添加剂D)的混合物。
然而,添加剂D)不包含含卤素的化合物、稀土金属盐或红磷。
本发明的热塑性模制组合物还可包含添加剂E)。不同添加剂的混合物也可被用作添加剂E)。添加剂E)可选自稳定剂、放静电剂、成核剂、加工助剂、抗冲改性剂、润滑剂以及脱模助剂、颜料和抗氧化剂。
可用的UV稳定剂的实例为取代的间苯二酚类化合物、水杨酸盐类化合物、苯并三唑类化合物和苯甲酮类化合物。
合适的无机颜料的实例为二氧化钛、群青蓝和/或炭黑,而可掺混的有机颜料的实例为二萘嵌苯类、酞菁类和/或喹吖酮类。染料同样适于使热塑性组合物着色,其实例为苯胺黑和/或蒽醌。
可使用的润滑剂和脱模剂为长链脂肪酸(例如硬脂酸)或其盐(例如硬脂酸钙)。润滑剂和脱模剂所通常使用的重量比为至多1%,基于热塑性模制组合物的总质量计。
可用的具体增塑剂为邻苯二甲酸二辛酯、邻苯二甲酸二苄酯、邻苯二甲酸丁基苄基酯、烃类油和/或N-正丁基苯磺酰胺。
然而,添加剂E)不包含含卤素的化合物、稀土金属盐或红磷。
组分A)、B)、C)、D)和E)可以各种重量比混合。下列重量百分比数据基于热塑性组合物的总质量。热塑性组合物中各重量百分比的总和为100重量%。
基于总质量,本发明的热塑性模制组合物包含例如40至60重量%的组分(A)。优选使用的(A)的重量比可为40至55重量%,特别是45至54重量%,基于热塑性模制组合物的总质量计。
优选本发明的热塑性模制组合物包含0.01至10重量%的组分B),基于热塑性模制组合物的总质量计。特别优选本发明的热塑性模制组合物包含0.01至8重量%,特别是1至8重量%的组分B),基于热塑性模制组合物的总质量计。
所加入的组分(C)的重量比为10至30重量%,基于热塑性模制组合物的总质量计。优选加入重量比为5至30重量%,特别是5至25重量%的组分C)。
所使用的增强剂(D)的重量比为0.01至60重量%,基于热塑性模制组合物的总质量计。在一个优选的实施方案中,热塑性模制组合物包含重量比为15至50重量%,特别是15至30重量%的添加剂,基于热塑性模制组合物的总质量计。
如果所述材料包含添加剂(E),则其所用的比例可为0至50重量%,基于热塑性模制组合物的总质量计。在一个优选的实施方案中,热塑性模制组合物包含重量比为1至50重量%,特别是1至45重量%的添加剂E),基于热塑性模制组合物的总质量计。
热塑性组合物中组成的实例
本发明的热塑性模制组合物的特征在于高耐漏电起痕性(CTI)以及不含卤素。所述模制组合物为阻燃剂。这表示所述热塑性模制组合物符合最严格的UL94燃烧测试要求并且符合涉及燃烧熔滴的燃烧测试要求。所述热塑性模制组合物的特征还在于良好的机械特性,特别是高缺口抗冲击性(缺口抗冲击性)。所述热塑性模制组合物还几乎没有内着色,原因是其不包含红磷。不含稀土金属盐是由于经济原因而期望的。
实施例
标准
ISO1183
塑料-测定非泡沫塑料密度的方法(Kunststoffe-Verfahren zurBestimmung der Dichte von nichtKunststoffen),德语版EN ISO1183:2004。
ISO1133
塑料-热塑性塑料熔体质量流动速率(MFR)和溶体体积流动速率(MVR)的测定(Kunststoffe-Bestimmung der Schmelze-Massefliessrate(MFR)und der SchmelzeVolumenfliessrate(MVR)vonThermoplasten);德语版EN ISO1133:2005。
UL94
“用于装置和设备中部件的塑料材料易燃性的测试(Test forflammability of plastic materials for parts in devices and appliances)”
IEC60112Edition4.1EN
“固体绝缘材料的耐漏电起痕指数和相对漏电起痕指数的测定方法(Method for the determination of the proof and the comparativetracking indices of solid insulating materials)”
组分
组分A-a
组分B-a
组分B-b
聚(丙烯-乙烯),购自LyondellBasell,密度(根据ISO1183测量)为0.9g/cm3且熔体流动指数MFR(根据ISO1133测量)为15g/10min(230℃,2.16kg),Moplen300N。
组分B-c
未改性的LDPE,密度(根据ISO1183测量)为0.917g/cm3且熔体流动指数MFR(根据ISO1133,塑料-热塑性塑料熔体质量流动速率(MFR)和溶体体积流动速率(MVR)的测定,德语版EN ISO1133:2005测量)为20g/10min(190℃,2.16kg),1800S。
组分c1-a
组分c1-b
组分c2-a
二乙基次膦酸铝,OP1230,购自Clariant。
组分D-a
玻璃纤维,直径10 m,标准纤维长度4.5mm,购自PPG的玻璃纤维3786。
组分E-a
加工
将所述组分在L/D比为18的双螺杆挤出机中挤出。该工艺期间的混合温度为260℃。生产能力为10kg/h。螺杆转速为300rpm。
短切所得的聚合物股线以得到粒料。将所述粒料在注塑工艺中进一步加工。
燃烧测试
根据UL94进行燃烧测试。此处所用样品的厚度为0.8mm。
耐漏电起痕性
根据IEC60112进行耐漏电起痕性测试。试样的尺寸为60mm x60mm x3mm。
实施例1至6
比较例1展示了未掺混聚烯烃的热塑性模制组合物。该实施例显示出使用聚烯烃提高了不含卤素的模制组合物的耐漏电起痕性(CTI)。同时该样品符合最严格的UL94燃烧测试要求并且符合涉及燃烧熔滴的燃烧测试要求。缺口抗冲击性也得到了保持。
Claims (11)
1.一种热塑性模制组合物,其不含卤素和稀土金属并且包含
A)40至60重量%的聚对苯二甲酸亚烷基酯
B)0.01至10重量%的选自下列的聚烯烃
b1)聚乙烯
b2)聚丙烯
b3)聚丙烯共聚物
以及它们的混合物;
C)10至30重量%的选自下列的阻燃剂
c1)含氮化合物
c2)含磷化合物
以及它们的混合物;
D)0.01至60重量%的增强剂;
E)0至50重量%的其它添加剂
其中重量比的总和为100重量%,基于热塑性模制组合物计。
2.权利要求1的热塑性模制组合物,其中A)为聚对苯二甲酸亚丁酯。
3.权利要求1或2的热塑性模制组合物,其中c2)选自磷酸盐、次磷酸盐和二次磷酸盐,以及它们的混合物。
4.权利要求1至3中至少一项的热塑性模制组合物,其中c1)为选自具有至少1个氮原子的含氮杂环的化合物。
5.权利要求1至4中至少一项的热塑性模制组合物,其中c1)为含三聚氰胺的阻燃剂。
6.权利要求1至5中至少一项的热塑性模制组合物,其中B)为聚丙烯。
7.权利要求1至5中至少一项的热塑性模制组合物,其中B)为聚(丙烯-乙烯)。
8.权利要求1至5中至少一项的热塑性模制组合物,其中B)为聚乙烯。
9.权利要求1至8中至少一项的热塑性模制组合物作为涂覆材料的用途。
10.权利要求1至8中至少一项的热塑性模制组合物用于制备纤维、箔或模制品的用途。
11.包含权利要求1至8中至少一项的热塑性模制组合物的纤维、箔或模制品。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11162549.7 | 2011-04-15 | ||
| EP11162549A EP2511337A1 (de) | 2011-04-15 | 2011-04-15 | Flammhemmende thermoplastische Formmasse |
| PCT/EP2012/056403 WO2012139990A1 (de) | 2011-04-15 | 2012-04-10 | Flammhemmende thermoplastische formmasse |
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| CN103476865A true CN103476865A (zh) | 2013-12-25 |
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|---|---|
| US (1) | US20120264856A1 (zh) |
| EP (2) | EP2511337A1 (zh) |
| JP (1) | JP2014511926A (zh) |
| KR (1) | KR101888817B1 (zh) |
| CN (1) | CN103476865A (zh) |
| BR (1) | BR112013025800A2 (zh) |
| WO (1) | WO2012139990A1 (zh) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8987357B2 (en) | 2011-05-27 | 2015-03-24 | Basf Se | Thermoplastic molding composition |
| HUE058033T2 (hu) | 2015-03-09 | 2022-06-28 | Lanxess Deutschland Gmbh | Hõre lágyuló formázómasszák |
| EP3067388A1 (de) | 2015-03-09 | 2016-09-14 | LANXESS Deutschland GmbH | Thermoplastische formmassen |
| US20250304767A1 (en) | 2022-05-12 | 2025-10-02 | Envalior Deutschland Gmbh | Creep-resistant polyester compositions |
| WO2024058384A1 (ko) * | 2022-09-16 | 2024-03-21 | (주) 엘지화학 | 폴리부틸렌 테레프탈레이트 수지 조성물, 이의 제조방법 및 이로부터 제조된 성형품 |
Citations (2)
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|---|---|---|---|---|
| JPH11335534A (ja) * | 1998-05-25 | 1999-12-07 | Toray Ind Inc | ハウジング用樹脂組成物およびそれからなるハウジング |
| WO2010078139A1 (en) * | 2008-12-30 | 2010-07-08 | Sabic Innovative Plastics Ip B.V. | Glass fiber reinforced polyester compositions, methods of manufacture, and articles thereof |
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| FR2154799B1 (zh) * | 1971-10-01 | 1979-06-15 | Gen Electric | |
| US5859099A (en) * | 1997-04-07 | 1999-01-12 | E. I. Du Pont De Nemours And Company | Flame retardant resin compositions |
| US5814690A (en) * | 1997-09-22 | 1998-09-29 | E. I. Du Pont De Nemours And Company | Flame retarded poly(butylene terephthalate) composition |
| JPH11335535A (ja) | 1998-05-25 | 1999-12-07 | Toray Ind Inc | 難燃性強化ポリブチレンテレフタレート製トランス部材用樹脂組成物およびそれからなるトランス部材 |
| JPH11335533A (ja) * | 1998-05-25 | 1999-12-07 | Toray Ind Inc | 難燃性強化ポリブチレンテレフタレート製コイルボビン用樹脂組成物およびそれからなるコイルボビン |
| JPH11335531A (ja) | 1998-05-25 | 1999-12-07 | Toray Ind Inc | 難燃性強化ポリブチレンテレフタレート樹脂組成物および成形品 |
| DE10126718A1 (de) | 2001-05-31 | 2002-12-05 | Basf Ag | Phosphor-Stickstoff-Kondensat, Verfahren zu dessen Herstellung und dessen Verwendung als Flammschutzmittel |
| DE10130832A1 (de) * | 2001-06-27 | 2003-01-16 | Bayer Ag | Flammwidrige Polyesterformmassen mit Polyolefinadditiven |
| JP2006056997A (ja) * | 2004-08-20 | 2006-03-02 | Mitsubishi Engineering Plastics Corp | ポリブチレンテレフタレート樹脂組成物及び成形品 |
| DE102004042833B4 (de) * | 2004-09-04 | 2022-01-05 | Chemische Fabrik Budenheim Kg | Polyphosphatderivat einer 1,3,5-Triazonverbindung, Verfahren zu dessen Herstellung und dessen Verwendung |
| KR101373241B1 (ko) | 2006-06-08 | 2014-03-19 | 주식회사 하우솔 | 무기소재를 이용한 환경친화형 난연성 폴리올레핀수지조성물 |
| DE102006058414A1 (de) * | 2006-12-12 | 2008-06-19 | Clariant International Limited | Carboxyethyl(alkyl)phosphinsäure-Alkylestersalze |
| JP4983328B2 (ja) * | 2007-03-26 | 2012-07-25 | 日立電線株式会社 | 高耐熱性樹脂組成物及びそれを用いた高耐熱絶縁電線 |
| DE102007041594A1 (de) * | 2007-09-01 | 2009-03-05 | Clariant International Limited | Flammwidrige Polyestercompounds |
| EP2062938A1 (en) * | 2007-11-26 | 2009-05-27 | Hitachi Cable, Ltd. | Insulated Wire Using a Resin Composition |
| CN101445650B (zh) | 2008-11-27 | 2012-03-07 | 北京华腾新材料股份有限公司 | 无卤阻燃聚对苯二甲酸乙二醇酯工程塑料复合材料及其制备方法 |
| CN101434727A (zh) | 2008-12-12 | 2009-05-20 | 暨南大学 | 一种无卤阻燃聚合物片材 |
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2011
- 2011-04-15 EP EP11162549A patent/EP2511337A1/de not_active Ceased
-
2012
- 2012-04-10 JP JP2014504272A patent/JP2014511926A/ja active Pending
- 2012-04-10 BR BR112013025800A patent/BR112013025800A2/pt not_active IP Right Cessation
- 2012-04-10 EP EP12713974.9A patent/EP2697306B1/de active Active
- 2012-04-10 KR KR1020137027049A patent/KR101888817B1/ko active Active
- 2012-04-10 CN CN201280018664XA patent/CN103476865A/zh active Pending
- 2012-04-10 WO PCT/EP2012/056403 patent/WO2012139990A1/de not_active Ceased
- 2012-04-13 US US13/446,069 patent/US20120264856A1/en not_active Abandoned
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| JPH11335534A (ja) * | 1998-05-25 | 1999-12-07 | Toray Ind Inc | ハウジング用樹脂組成物およびそれからなるハウジング |
| WO2010078139A1 (en) * | 2008-12-30 | 2010-07-08 | Sabic Innovative Plastics Ip B.V. | Glass fiber reinforced polyester compositions, methods of manufacture, and articles thereof |
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Also Published As
| Publication number | Publication date |
|---|---|
| US20120264856A1 (en) | 2012-10-18 |
| JP2014511926A (ja) | 2014-05-19 |
| KR101888817B1 (ko) | 2018-08-16 |
| EP2511337A1 (de) | 2012-10-17 |
| WO2012139990A1 (de) | 2012-10-18 |
| BR112013025800A2 (pt) | 2016-12-20 |
| EP2697306A1 (de) | 2014-02-19 |
| EP2697306B1 (de) | 2016-03-02 |
| KR20140027151A (ko) | 2014-03-06 |
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