TWI756530B - 發泡熱塑性聚氨基甲酸酯及其微波成型體 - Google Patents
發泡熱塑性聚氨基甲酸酯及其微波成型體 Download PDFInfo
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Abstract
一種可發泡組合物用以製作發泡熱塑性聚氨基甲酸酯及其微波成型體,該可發泡組合物包括未發泡熱塑性聚氨基甲酸酯粒子、增黏劑或架橋劑,以及發泡劑,其中該未發泡熱塑性聚氨基甲酸酯粒子具有1,000泊至9,000泊之黏度,該黏度以JISK 7311測試方法在170℃測得。
Description
本發明係關於一種發泡熱塑性聚氨基甲酸酯以及其經微波所製成的成型體。
熱塑性聚氨基甲酸酯(thermoplastic polyurethane,TPU)為熱塑性彈性體(thermoplastic elastomer,TPE)的原材料。以TPU製成的TPE具備黏性、高彈性、耐磨性、耐衝擊性、耐曲折性、高延伸性、耐候性、耐化學性、無毒性及高抗撕裂強度等諸多優點,故已被廣泛應用於如鞋子、汽車、包裝材料、絕熱材料等產品中。
射出成型是現有技術中製備TPU發泡成型體最常用的方法。射出成型的製程涉及塑橡膠粒在射出成型機內加熱熔化,然後壓縮熔融使其移動通過噴嘴注入溫度較低的模具內,生產流程長甚為耗時。而且射出用的模具重量相當重,導致更換模具相當不便。現有技術另有一種採用水蒸氣成型法製備TPU發泡成型體。然而,水蒸氣成型法需涉及高溫或高壓製程,往往需消耗更多的能源,導致成本增加。有別於射出成型法及水蒸氣成型法,以微波方法所製造的成型體製程簡單且省時省能源。微波TPU發泡成型體已可應用於各類產品。舉例而言,微波TPU發泡成型體已成功地應用於鞋子上,其能兼具舒適性、靈活性及輕質等優點。
然而,可發泡組合物中所含未發泡熱塑性聚氨基甲酸酯粒子,其黏度通常限制在10,000泊以上,才適用於形成微波TPU發泡成型體。若使用黏度低於10,000泊之未發泡粒子,其所形成的發泡粒子經微波後,具有低劣發泡的現象,導致微波成型體有成型不良(如外觀易變型、塌陷、粒子間黏著不佳、成型穩定性不佳)之問題。
本發明意外地發現可使用增黏劑或架橋劑來改善上述之問題。添加增黏劑或架橋劑,可使聚氨基甲酸酯粒子的黏彈性質或分子鍵結結構的改變,進而增強分子鏈間結構強度。本發明係提供一種適用於微波成型體的可發泡組合物,包含1,000泊至9,000泊之黏度的未發泡熱塑性聚氨基甲酸酯粒子,及增黏劑或架橋劑,該黏度以JISK 7311測試方法在170℃測得。
本發明於一方面提供製作發泡熱塑性聚氨基甲酸酯的可發泡組合物(也可稱作配方)、將上述組合物經過發泡造粒所製成的發泡熱塑性聚氨基甲酸酯,以及其發泡造粒的方法。本發明之發泡熱塑性聚氨基甲酸酯具有經微波可再次發泡的特性,因此本發明更提供將上述之發泡熱塑性聚氨基甲酸酯微波後二次發泡的微波成型體及其製造方法。本發明之發泡熱塑性聚氨基甲酸酯具有更具輕質之優點,藉由微波加熱發泡熱塑性聚氨基甲酸酯後各粒子表面將產生黏合作用,且同時再次發泡以形成微波成型體(或稱為熱塑性聚氨基甲酸酯發泡材料)。有別於現有的射出成型法及水蒸氣成型法,以微波方法所製造的成型體製程簡單且省時省能源。
於一實施例,本發明提供一種可發泡組合物用以製作發泡熱塑性聚氨基甲酸酯,該可發泡組合物包括100重量份之一未發泡熱塑性聚氨基甲酸酯粒子、5重量份至25重量份之一發泡劑,及0.5重量份至5重量份之一增黏劑或一架橋劑,其中該未發泡熱塑性聚氨基甲酸酯粒子具有1,000 泊至9,000泊之黏度,該黏度以JISK 7311測試方法在170℃測得。
於一實施例,本發明提供如上述之可發泡組合物,其中該增黏劑係選自無機增稠劑、聚丙烯酸類增稠劑、或纖維素類增稠劑。
於一實施例,本發明提供如上述之之可發泡組合物,其中架橋劑係選自過氧化二異丙苯(DCP)、過氧化苯甲醯、二叔丁基過氧化物、或過氧化氫二異丙苯2,5-二甲基-2,5二叔丁基過氧化己烷。
於一實施例,本發明提供如上述之可發泡組合物,其中該無機增稠劑係選自膨潤土或矽酸鋁,該聚丙烯酸類增稠劑係選自丙烯酸、馬來酸、馬來酸酐或甲基丙烯酸之羧酸類單體形成的增稠劑,該聚丙烯酸類增稠劑係選自甲基纖維素、羧甲基纖維素、羥乙基纖維素、或羥丙基甲基纖維素所形成的增稠劑。
於一實施例,本發明提供如上述之可發泡組合物,其中該未發泡熱塑性聚氨基甲酸酯粒子具有2.5mm至4.5mm的粒徑。
於一實施例,本發明提供如上述之可發泡組合物,其中該未發泡熱塑性聚氨基甲酸酯粒子具有40A至64D的肖氏硬度。
於一實施例,本發明提供如上述之可發泡組合物,其中該未發泡熱塑性聚氨基甲酸酯粒子具有1.0g/cm3至1.25g/cm3的密度。
於一實施例,本發明提供如上述之可發泡組合物,包含100重量份之該未發泡熱塑性聚氨基甲酸酯粒子及5重量份至20重量份之該發泡劑。
於一實施例,本發明提供如上述之可發泡組合物,其中該發泡劑為膨脹性微球、二氧化碳(CO2)、或碳數為4至10之烴類化合物。
於一實施例,本發明提供如上述之可發泡組合物,更包含0.1重量份至5重量份之滑石粉。
於一實施例,本發明提供如上述之可發泡組合物,更包含1重量份至20重量份之可塑劑,該可塑劑為苯甲酸酯或其衍生物。
於一實施例,本發明提供如上述之可發泡組合物,更包含色粉,基於100重量份的該未發泡熱塑性聚氨基甲酸酯粒子,該色粉含有0.1重量份至5重量份。
於一實施例,本發明提供如上述之可發泡組合物,更包含1重量份至5重量份之該增黏劑或該架橋劑。
於一實施例,本發明提供一種發泡熱塑性聚氨基甲酸酯,係將採用上述任一項所述之可發泡組合物經一螺桿造粒機發泡造粒製成。
於一實施例,本發明提供如上述之發泡熱塑性聚氨基甲酸酯,其中該發泡熱塑性聚氨基甲酸酯具有殘留的該發泡劑。
於一實施例,本發明提供如上述之發泡熱塑性聚氨基甲酸酯,其中該發泡熱塑性聚氨基甲酸酯具有3mm至7.5mm的粒徑。
於一實施例,本發明提供如上述之發泡熱塑性聚氨基甲酸酯,其中該發泡熱塑性聚氨基甲酸酯具有40C至80C的肖氏硬度。
於一實施例,本發明提供如上述之發泡熱塑性聚氨基甲酸酯,其中該發泡熱塑性聚氨基甲酸酯具有0.2g/cm3至0.8g/cm3的密度。
於一實施例本發明提供一種微波成型體,其係將上述之發泡熱塑性聚氨基甲酸酯經微波而成。
於一實施例,本發明提供如上述之微波成型體,其中該微波成型體之密度為0.15g/cm3至0.6g/cm3。
於一實施例,本發明提供如上述之微波成型體,其中該微波成型體之肖氏硬度為40C至80C。
於一實施例,本發明提供如上述之微波成型體,其中該微波成型體是經由500W至30,000W微波功率製成。
於一實施例,本發明提供如上述之微波成型體,其中該微波之過程中不加水。
於一實施例,本發明提供如上述之微波成型體,其中該微波 之過程中加水或醇類,以該發泡熱塑性聚氨基甲酸酯之總重為100重量份,該水或醇類之用量為1重量份至10重量份。
本發明尚包含其他各方面及各種微波成型體,以解決其他問題並合併上述之各方面詳細揭露於以下實施方式中。
為使本發明及其所要主張的申請專利範圍能被充分地理解,以下將示範本發明之較佳實施例。為避免模糊本發明之內容,以下說明可能會省略習知的元件、相關材料、及其相關處理技術。
製作發泡熱塑性聚氨基甲酸酯的可發泡組合物
本發明製作發泡熱塑性聚氨基甲酸酯的可發泡組合物主要包含未發泡熱塑性聚氨基甲酸酯粒子、增黏劑或架橋劑、及發泡劑。組合物中未發泡熱塑性聚氨基甲酸酯粒子具有在1,000泊至9,000泊之黏度,可使首次發泡的粒子具有良好的再次發泡功能。黏度是以JISK 7311測試方法在170℃度測得。未發泡熱塑性聚氨基甲酸酯粒子具有在3,000泊至8,000泊之黏度者為更佳,其除可使首次發泡的粒子達成良好的再次發泡功能外,再次發泡後材料將有更佳的機械強度。
100重量份之未發泡熱塑性聚氨基甲酸酯粒子中,增黏劑或架橋劑之含量以0.5重量份至5重量份為較佳。100重量份之未發泡熱塑性聚氨基甲酸酯粒子中,發泡劑之含量以5重量份至25重量份為較佳,若要有更佳的機械強度,以5重量份至20重量份為更佳。依據本發明之各實施例,組合物中未發泡熱塑性聚氨基甲酸酯粒子優選具有2.5mm至4.5mm(millimeter即毫米)的粒徑者。本發明所述之粒徑是指量測粒子的最長軸。依據本發明之其他實施例,組合物中未發泡熱塑性聚氨基甲酸酯粒子優選具有40A至64D的肖氏硬度者。依據本發明之再其他的實施例,組合物中未發泡熱塑性聚氨基甲酸酯粒子優選具有1.0g/cm3至1.25g/cm3的密度者。 本文所指密度均以阿基米德原理(浮力法)測得。
本發明之發泡熱塑性聚氨基甲酸酯具有良好的再次發泡特性。所謂『再次發泡』特性是指經過首次發泡所形成的發泡熱塑性聚氨基甲酸酯,本身可再次(二次)發泡,特別是經由微波來再次發泡。此類發泡熱塑性聚氨基甲酸酯再次發泡後其粒子明顯膨脹且粒子間可黏合緊密而呈現形狀飽滿之發泡成型體,此為良好再次發泡。
可發泡組合物中未發泡熱塑性聚氨基甲酸酯粒子可為酯類、醚類、聚己內酯類或聚碳酸酯類。未發泡熱塑性聚氨基甲酸酯粒子的作法,舉例而言,可將二異氰酸酯、聚酯多元醇、增鏈劑、催化劑和其他的添加劑相混合在約200~300℃下反應並通過習知的注塑或擠出處理以獲得未發泡熱塑性聚氨基甲酸酯粒子。二異氰酸酯可選自4,4_亞甲基雙(苯基異氰酸酯)(MDI)、間-亞二甲苯基二異氰酸酯(XDI)、亞苯基-1,4-二異氰酸酯、1,5-萘二異氰酸酯、甲苯二異氰酸酯(TDI)、異佛爾酮二異氰酸酯(IPDI)、六亞甲基二異氰酸酯(HDI)和二環己基甲烷-4,4-二異氰酸酯。較佳為MDI或TDI。聚酯多元醇為二元酸和二元醇的聚酯類,二元醇可為具有2-10個碳原子的二元醇,二元酸可為具有4-12個碳原子的直鏈或支鏈的二元酸。較佳為己二酸1,4-丁二醇酯。增鏈劑是具有2-12個碳原子的二醇;例如:乙二醇、二甘醇、丙二醇、二丙二醇、1,4-丁二醇、1,6-己二醇、1,3-丁二醇、1,5-戊二醇、1,4-環己烷二甲醇、新戊二醇、苯二醇和二甲苯二醇中的至少一種。催化劑可選自三乙胺、二甲基環己胺、二辛酸亞錫、二辛酸二丁基錫、二月桂酸二丁基錫、二乙酸二丁基錫中的至少一種。注塑或擠出處理過程中也可使用各種添加劑、譬如顏料、填料、抗氧劑、增強劑、潤滑劑或增塑劑等等。
可發泡組合物含有增黏劑或架橋劑。增黏劑可為無機增稠劑(例如;膨潤土、矽酸鋁等)、聚丙烯酸類增稠劑(例如:羧酸類單體,如丙烯酸、馬來酸或馬來酸酐、甲基丙烯酸等)、纖維素類增稠劑(甲基纖維素、 羧甲基纖維素、羥乙基纖維素、羥丙基甲基纖維素等)。架橋劑可為過氧化二異丙苯(DCP)、過氧化苯甲醯、二叔丁基過氧化物、過氧化氫二異丙苯2,5-二甲基-2,5二叔丁基過氧化己烷等。
可發泡組合物中發泡劑可為有機發泡劑或無機發泡劑。有機發泡劑的實例,譬如偶氮化合物(例如:偶氮二甲醯胺、偶氮二異丁腈、偶氮二甲酸二異丙酯)、磺醯胺類化合物(例如:4,4-氧代雙苯磺醯肼、對苯磺酰肼、1,4-苯二磺酰肼)、亞硝基化合物(例如:二亞硝基對苯二甲醯胺、N,N’-二亞硝基五次甲基四胺)、二氧化碳(CO2)、碳數為4至10之烴類化合物(例如:正戊烷、異戊烷與環戊烷)或膨脹性微球(例如:可膨脹性微膠囊、微球發泡粉)。其中以可膨脹性微球為更佳。
本發明製作發泡熱塑性聚氨基甲酸酯的可發泡組合物除了未發泡熱塑性聚氨基甲酸酯粒子、增黏劑或架橋劑、以及發泡劑外,還可視需要包含無機填充物及可塑劑。無機填充物例如用作脫模劑的滑石粉、雲母粉、硫代硫酸鈉等。較佳係使用滑石粉。依據各種實施例,基於100重量份的未發泡熱塑性聚氨基甲酸酯粒子,較佳係含有0.1重量份至5重量份之滑石粉為更佳。可塑劑可為安息香酸類化合物(例如:苯甲酸酯、如苯甲酸甲酯、苯甲酸乙酯、二苯甲酸二丙二醇酯等、及其衍生物)、酯類化合物(例如:檸檬酸三乙酯、檸檬酸三甲酯、檸檬酸乙醯基三乙酯、及其衍生物)、醚類化合物(例如:己二酸醚酯、乙二醇丁醚酯、及其衍生物)、聚己內酯類化合物(例如:聚己內酯二醇、及其衍生物)或聚碳酸酯類化合物(例如:聚碳酸甲酯、聚碳酸苯酯、及其衍生物)。較佳使用苯甲酸酯或其衍生物。依據各種實施例,基於100重量份的未發泡熱塑性聚氨基甲酸酯粒子,較佳係含有1重量份至20重量份之可塑劑。
於一較佳實施例,本發明製作發泡熱塑性聚氨基甲酸酯的可發泡組合物具有以下配比:100重量份之未發泡熱塑性聚氨基甲酸酯粒子;0.5重量份至5重量份之增黏劑或架橋劑;0.1重量份至5重量份之滑石粉;1 重量份至20重量份之可塑劑;以及5重量份至25重量份之發泡劑,組合物中未發泡熱塑性聚氨基甲酸酯粒子具有在1,000泊至9,000泊之黏度,該黏度以JISK 7311測試方法在170℃測得。在滑石粉及可塑劑皆有需要加入組合物的狀況下,上述配比有助於形成具有孔洞大小均勻及粒徑一致的發泡熱塑性聚氨基甲酸酯。
此外,可發泡組合物中也可以添加各種顏色的色粉。依據各種實施例,基於100重量份的未發泡熱塑性聚氨基甲酸酯粒子,較佳係含有0.1重量份至5重量份的色粉。
製作發泡熱塑性聚氨基甲酸酯的方法
以下舉例說明進行發泡造粒以製作發泡熱塑性聚氨基甲酸酯的方法。首先將符合前述之可發泡組合物(含未發泡熱塑性聚氨基甲酸酯粒子、增黏劑或架橋劑、及發泡劑、或可視需要添加無機填料、可塑劑、色料等等)投入一單螺桿造粒機中以進行發泡造粒。所述之單螺桿造粒機的模頭溫度可為100℃至180℃,擠壓速度可為50kg/h至70kg/h,模頭壓力可為35kgf/cm2至65kgf/cm2,水中造粒溫度可為10℃至20℃;再更佳的,所述之單螺桿造粒機的模頭溫度可為110℃至165℃,或再更佳110℃到150℃。可使用上述之發泡造粒法或其他合適方法製作發泡熱塑性聚氨基甲酸酯。注意擠壓速度過低將可能導致造粒發泡粒子過發(稱螺桿過發),造成無法再經微波發泡。
可依據上述之方法配製發泡熱塑性聚氨基甲酸酯具有多種顏色的單一粒子。舉例而言,可先準備多種含單色料的可發泡組合物,每種顏色不同,譬如第一可發泡組合物(含黑色料)及第二可發泡組合物(含紅色料)。然後,將第一組合物分多次投入單螺桿造粒機中,在該第一組合物的該多次投入中任選兩次,在所任選的兩次之間投入一部分的該第二可發泡組合物。以此方法類推可配製發泡熱塑性聚氨基甲酸酯具有多種顏色的單一粒子。
發泡熱塑性聚氨基甲酸酯
可依據前述之可發泡組合物與方法製造本發明之發泡熱塑性聚氨基甲酸酯,但不此為限。較佳而言,本發明之發泡熱塑性聚氨基甲酸酯具有可再發泡性質,換言之,本發明之發泡熱塑性聚氨基甲酸酯可透過譬如微波等合適方法再次發泡,而產生更低密度。具體而言,在各較佳實例中,本發明提供具有一密度範圍為0.2g/cm3至0.8g/cm3的發泡熱塑性聚氨基甲酸酯,將此發泡熱塑性聚氨基甲酸酯施以微波可使其再次發泡而產生比首次發泡的密度更低的再次發泡的密度,範圍為0.15g/cm3至0.6g/cm3。在本文中,前述組合物經造粒發泡形成發泡熱塑性聚氨基甲酸酯,此段製程稱為第一段發泡。第一段發泡所製得的發泡熱塑性聚氨基甲酸酯再進行發泡,此段製程稱為第二段發泡。在一較佳實施例中,第一段發泡之發泡熱塑性聚氨基甲酸酯係殘留發泡劑,但本發明不以此為限。調整可發泡組合物的配方或控制造粒發泡的製程而使發泡熱塑性聚氨基甲酸酯中殘留尚未完全失效的發泡劑,將可加強其再次發泡的能力。依據本發明之實施例,第一段發泡之發泡熱塑性聚氨基甲酸酯較佳具有3mm至7.5mm的粒徑。依據本發明之其他實施例,第一段發泡之發泡熱塑性聚氨基甲酸酯較佳具有40C至80C的肖氏硬度。依據本發明之再其他的實施例,第一段發泡之發泡熱塑性聚氨基甲酸酯較佳具有0.2g/cm3至0.8g/cm3的密度。第一段發泡之發泡熱塑性聚氨基甲酸酯可有各種外型,譬如球狀、薄片狀、非球狀之不規則狀等等。
微波成型體及其方法
本發明微波成型體係以微波方式進行第二段發泡而成,其經微波所製得之發泡材料中形成之孔洞將比未經過微波的更加均勻細緻,更具有輕質之優點。此外,藉由微波也使發泡熱塑性聚氨基甲酸酯之各個粒子表面產生相互黏合作用,進而成為微波成型體。依據各種實施例,本發明所製作之微波成型體可優選地具有以下物性:較佳硬度肖氏為40C至 80C;較佳密度為0.15g/cm3至0.6g/cm3。
依據各種實施例,本發明微波成型體製法可為:取適當量之第一段發泡之發泡熱塑性聚氨基甲酸酯置入一容器中,然後照射微波,此容器可為各種模具。陶瓷模具、塑膠模具、玻璃模具或金屬與塑膠複合模具,於較佳實施例容器為金屬與塑膠複合材。本發明於進行微波發泡製程中,頻率為2450MHz微波,較佳的微波功率為500瓦(W)至30,000W,更佳為5,000W至25,000W,微波時間為3秒至300秒,更佳為5秒到120秒。依據某些實施例,微波過程中不需加水。於某些實施例微波過程中可加入水或醇類等作為微波介質。在此等實施例中,基於100重量份的發泡熱塑性聚氨基甲酸酯,該介質之用量為1重量份至10重量份。該介質可為極性介質,可選用之醇類包括一級醇(例如:甲醇或乙醇)及二級醇(例如:乙二醇或丙二醇),但並非僅限於此。
綜上所述,藉由提供有合適配比的可發泡組合物,依序進行第一段發泡造粒製程及第二段微波發泡製程,即可產出兼具輕質(發泡倍率高)、質量穩定、孔洞分佈均勻等優點之熱塑性聚氨基甲酸酯發泡材料。
以下列舉各種實例詳細說明本發明之實施方式。熟習此技藝者可經由本說明書之內容輕易地了解本發明所能達成之優點與功效,並且於不悖離本發明之精神下進行各種修飾與變更,以施行或應用本創作之內容。
第一段造粒發泡:實例1a、實例2a及比較例1a’
實例1a:將100重量份的未發泡熱塑性聚氨基甲酸酯粒子(商品名稱:T955PLVM2,肖氏硬度為50A,黏度為9000泊(170℃),由三晃股份有限公司製造)、2.5重量份的苯甲酸甲酯(作為可塑劑)、2.5重量份的矽酸鋁(作為增黏劑)、0.1重量份的滑石粉及15重量份的膨脹性微球(商品名稱:Expancel 930DU-120,購自Matsumoto,作為發泡劑)均勻混合後,投入單螺桿造粒機,以物料擠壓速度為50kg/h、模頭壓力為50kgf/cm2、模頭溫度為 155℃、螺桿溫度120-170℃及水中造粒溫度為20℃之條件進行第一段發泡造粒製程,以獲得一次發泡熱塑性聚氨基甲酸酯。此一次發泡熱塑性聚氨基甲酸酯的密度為0.33g/cm3,為粒狀。
實例2a:將100重量份的未發泡熱塑性聚氨基甲酸酯粒子(商品名稱:T955PLVM2,肖氏硬度為50A,黏度為9000泊(170℃),由三晃股份有限公司製造)、2.5重量份的苯甲酸甲酯(作為可塑劑)及1.0重量份的過氧化二異丙苯(作為架橋劑)、0.1重量份的滑石粉及15重量份的膨脹性微球(商品名稱:Expancel 930DU-120,購自Matsumoto,作為發泡劑)均勻混合後,投入單螺桿造粒機,以物料擠壓速度為50kg/h、模頭壓力為50kgf/cm2、模頭溫度為155℃、螺桿溫度120-170℃及水中造粒溫度為20℃之條件進行第一段發泡造粒製程,以獲得一次發泡熱塑性聚氨基甲酸酯。此一次發泡熱塑性聚氨基甲酸酯的密度為0.32g/cm3,為粒狀。
比較例1a’:將100重量份的未發泡熱塑性聚氨基甲酸酯粒子(T955PLVM2,肖氏硬度為50A,黏度為9000泊(170度),由三晃股份有限公司製造)、2.5重量份的苯甲酸甲酯(作為可塑劑)、0.1重量份的滑石粉及15重量份的膨脹性微球(商品名稱:Expancel 930DU-120,購自Matsumoto,作為發泡劑)均勻混合後,投入單螺桿造粒機,以物料擠壓速度為50kg/h、模頭壓力為35kgf/cm2、模頭溫度為155℃、螺桿溫度120-170℃及水中造粒溫度為20℃之條件進行第一段發泡造粒製程進行第一段發泡造粒製程,未加入增黏劑、架橋架,此一次發泡熱塑性聚氨基甲酸酯的密度為0.48g/cm3,為粒狀。
第二段微波發泡:實例1b、實例2b及比較例1b’
實例1b:將前述實例1a所製得之發泡熱塑性聚氨基甲酸酯(名稱為1a)取72重量份並加入3重量份的水置入模具中,該模具之長度為20公分、寬度為12公分、高度為1.2公分,再以微波頻率為2450MHz,微波功率為8000W、微波時間為35秒進行第二段微波發泡製程,待模具降溫冷卻 後,即完成熱塑性聚氨基甲酸酯微波成型體,平均密度為0.27g/cm3。
實例2b、實例2b及比較例1b’可參考實例1b之作法。各實例之條件可參考表1及表2的說明。
實例與比較例的分析討論
實例1a/1b、2a/2b、與比較例1a/1b(添加增稠劑/架橋劑)
比較例1a’與實例1a的差異在於實例1a有使用增稠劑。比較例1a’與實例2a的差異在於實例2a有使用架橋劑。由於比較例1a無使用增稠劑或架橋劑,因此發泡熱塑性聚氨基甲酸酯在一次發泡階段由於黏度過低,強度不足,導致發泡粒子無法穩定成型,造成冷卻時粒子有明顯收縮現象,因而密度提升。比較例1a雖可順利獲得已發泡熱塑性聚氨基甲酸酯(密度0.48g/cm3),但此粒子經微波後膨脹性不佳,因而塌陷無法呈現形狀飽滿之微波發泡成型體。
Claims (18)
- 一種微波成型體,係將一發泡熱塑性聚氨基甲酸酯經微波而成,該發泡熱塑性聚氨基甲酸酯係由一可發泡組合物經一螺桿造粒機發泡造粒製成,該可發泡組合物包括:100重量份之一未發泡熱塑性聚氨基甲酸酯粒子、5重量份至25重量份之一發泡劑,及0.5重量份至5重量份之一增黏劑或一架橋劑,其中該未發泡熱塑性聚氨基甲酸酯粒子具有1,000泊至9,000泊之黏度,該黏度以JISK 7311測試方法在170℃測得。
- 如請求項1所述之微波成型體,其中該微波成型體之密度為0.15g/cm3至0.6g/cm3。
- 如請求項1所述之微波成型體,其中該微波成型體之肖氏硬度為40C至80C。
- 如請求項1所述之微波成型體,其中該增黏劑係選自無機增稠劑、聚丙烯酸類增稠劑、或纖維素類增稠劑。
- 如請求項1所述之微波成型體,其中架橋劑係選自過氧化二異丙苯(DCP)、過氧化苯甲醯、二叔丁基過氧化物、或過氧化氫二異丙苯2,5-二甲基-2,5二叔丁基過氧化己烷。
- 如請求項4所述之微波成型體,其中該無機增稠劑係選自膨潤土或矽酸鋁,該聚丙烯酸類增稠劑係選自丙烯酸、馬來酸、馬來酸酐或甲基丙烯酸之羧酸類單體形成的增稠劑,該纖維素類增稠劑係選自甲基纖維素、羧甲基纖維素、羥乙基纖維素、或羥丙基甲基纖維素所形成的增稠劑。
- 如請求項1所述之微波成型體,其中該未發泡熱塑性聚氨基甲酸酯粒子具有2.5mm至4.5mm的粒徑。
- 如請求項1所述之微波成型體,其中該未發泡熱塑性聚氨基甲酸酯粒子具有40A至64D的肖氏硬度。
- 如請求項1所述之微波成型體,其中該未發泡熱塑性聚氨基甲酸酯粒子具有1.0g/cm3至1.25g/cm3的密度。
- 如請求項1所述之微波成型體,包含100重量份之該未發泡熱塑性聚氨基甲酸酯粒子及5重量份至20重量份之該發泡劑。
- 如請求項1所述之微波成型體,其中該發泡劑為膨脹性微球、二氧化碳(CO2)、或碳數為4至10之烴類化合物。
- 如請求項1所述之微波成型體,更包含0.1重量份至5重量份之滑石粉。
- 如請求項1所述之微波成型體,更包含1重量份至20重量份之可塑劑,該可塑劑為苯甲酸酯或其衍生物。
- 如請求項1所述之微波成型體,更包含色粉,基於100重量份的該未發泡熱塑性聚氨基甲酸酯粒子,該色粉含有0.1重量份至5重量份。
- 如請求項1所述之微波成型體,更包含1重量份至5重量份之該增黏劑或該架橋劑。
- 如請求項1所述之微波成型體,其中該微波成型體是經由500W至30,000W微波功率製成。
- 如請求項1所述之微波成型體,其中該微波之過程中不加水。
- 如請求項1所述之微波成型體,其中該微波之過程中加水或醇類,以該發泡熱塑性聚氨基甲酸酯之總重為100重量份,該水或醇類之用量為1重量份至10重量份。
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US20210214515A1 (en) | 2021-07-15 |
WO2019237280A1 (zh) | 2019-12-19 |
JP2021526577A (ja) | 2021-10-07 |
CN112166157B (zh) | 2021-10-29 |
EP3808814A4 (en) | 2022-02-23 |
US11993689B2 (en) | 2024-05-28 |
JP7090749B2 (ja) | 2022-06-24 |
CN112166157A (zh) | 2021-01-01 |
EP3808814A1 (en) | 2021-04-21 |
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