TW202206664A - 絕熱材料、製備絕熱材料之方法、及由絕熱材料製備之產品 - Google Patents
絕熱材料、製備絕熱材料之方法、及由絕熱材料製備之產品 Download PDFInfo
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- TW202206664A TW202206664A TW110126242A TW110126242A TW202206664A TW 202206664 A TW202206664 A TW 202206664A TW 110126242 A TW110126242 A TW 110126242A TW 110126242 A TW110126242 A TW 110126242A TW 202206664 A TW202206664 A TW 202206664A
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- thermal insulation
- insulation material
- woven fabric
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Abstract
本揭露之實施例中提供一種絕熱材料、一種製備絕熱材料之方法、及一種由絕熱材料製備之產品。本揭露之實施例之絕熱材料包含：一不織布基材，其在1kPa的一壓力下具有至少70%的一厚度留存比率；一乾凝膠；及一陽離子界面活性劑，其包含四級銨鹽，並均勻地分散在該乾凝膠中；其中該不織布基材在該絕熱材料中之含量按重量百分比係20%至96.7%，該乾凝膠在該絕熱材料中之含量按重量百分比係3%至60%，且該陽離子界面活性劑在該絕熱材料中之含量按重量百分比係0.3%至20%。
Description
本申請案係關於絕熱材料、製備絕熱材料之方法、及由絕熱材料製備之產品。具體而言，本申請案係關於包括乾凝膠之絕熱材料、製備絕熱材料之方法、及其產品。
絕熱材料係廣泛地用在服裝、鞋、手套等之中或者用在寢具(諸如被褥)之中。為了達成絕熱效應，大多數的絕熱材料結構可在其中留置空氣，從而減少熱能消散。
在空間有限及需要絕熱效應的一些應用中(例如在鞋類應用中)，絕熱材料將經壓縮，且因此影響絕熱效應。因此，目前存在利用氣凝膠或乾凝膠之低密度及孔隙度的特性以維持絕熱效應的技術。
在一些文件中，用語「乾凝膠(xerogel)」及「氣凝膠(aerogel)」係用以描述藉由乾燥凝膠所形成的多孔固體。通常，乾凝膠與氣凝膠之間的差異係基於結構的孔隙度及密度。乾凝膠之孔
隙度通常係20%至40%，且其密度係0.5至0.8g/cc；而氣凝膠的密度通常係0.1至0.2g/cc，且其孔隙度係至少75%。
然而，氣凝膠或乾凝膠由於許多孔洞的存在而易碎，且因此僅適用於有限的領域。在壓縮狀態下如何維持結構完整性亦係重要問題。在現有氣凝膠或乾凝膠產品中，存在使用各種技術以增加其溶膠之實體結構強度者。例如，在WO 2013053951中，在製備乾凝膠的程序中使用纖維強化材料；WO 1997023675 A2中揭示藉由熱塑性纖維及氣凝膠粒子形成的複合材料；WO 2017087511中揭示合成纖維，其包括氣凝膠粒子及聚合物材料；且US 20160060808 A1中揭示隔熱片材，其含有矽石乾凝膠及不織布。然而，這些現有技術仍無法克服氣凝膠或乾凝膠之易碎性問題；此外，許多製備氣凝膠的製程使用次臨界或超臨界條件，或者需要溶劑交換以供製備(諸如CN 102964111 A)，且因此程序涉及複雜的步驟及高花費。
此外，亦存在一些技術，其中聚合物係覆蓋在氣凝膠或乾凝膠的表面上以克服易碎性問題，但這些方法將犧牲絕熱材料的透氣性及增加其重量。
有鑑於此，本揭露之實施例中提供一種絕熱材料、一種製備絕熱材料之方法、及一種由絕熱材料製備之產品。本揭露之實施例中所提供的絕熱材料不需在嚴苛條件(諸如超臨界及次臨界條件)下或經由溶劑交換方法製備，且因此有助於簡化製備程序及降低製備成本，且所得的絕熱材料仍維持某些結構強度、絕熱位準、
及透氣性，並可因此廣泛地適用於各種產品。此外，由於本揭露之實施例之絕熱材料進一步具有抗菌性質之優點，且亦在壓縮狀態下經由穩定結構維持絕熱效應，該絕熱材料亦可適用於易於孳生細菌的環境(諸如但不限於鞋類)。
通常，本揭露之實施例中所述的絕熱材料包含一不織布基材、一乾凝膠、及一陽離子界面活性劑。該不織布基材在1kPa的一壓力下具有至少70%的一厚度留存比率。該陽離子界面活性劑包括四級銨鹽，且係均勻地分散在該乾凝膠中，其中該不織布基材在該絕熱材料中之含量按重量百分比係20%至96.7%，該乾凝膠在該絕熱材料中之含量按重量百分比係3%至60%，且該陽離子界面活性劑在該絕熱材料中之含量按重量百分比係0.3%至20%。
在一些實施例中，該不織布基材之該材料係選自下列中之至少一者：一聚酯纖維、一尼龍纖維、一丙烯酸纖維、一聚丙烯纖維、一聚乳酸纖維、及一纖維素纖維。
在一些實施例中，該不織布基材在0.02kPa之一壓力下的初始厚度係2至50mm。
在一些實施例中，該乾凝膠係由包含一有機矽氧化物前驅物的一膠體形成，且該有機矽包含一烷氧基矽烷。
在一些實施例中，該烷氧基矽烷包含一烷基三烷氧基矽烷，且可選地該烷基三烷氧基矽烷係甲基三甲氧基矽烷、乙烯基三甲氧基矽烷、及其組合；或者，該烷氧基矽烷包含一二烷氧基矽
烷，且可選地，該二烷氧基矽烷係選自二乙氧基矽烷、三甲氧基矽烷、及其組合。
在一些實施例中，該膠體進一步包含一溶劑及一催化劑。該溶劑包含一醇(例如甲醇、乙醇、或其一組合)；該催化劑包含一酸性催化劑(諸如草酸、鹽酸、或其一組合)及一鹼性催化劑(諸如氫氧化銨、脲、或其一組合)。
在一些實施例中，該陽離子界面活性劑之該四級銨鹽係選自四級銨鹵素鹽(例如，十六基三甲基溴化銨、十六基三甲基氯化銨、溴化苄烷銨、氯化苄烷銨、或其一組合)。
本揭露之實施例中進一步提供一種製備絕熱材料之方法，其包含：(a)提供一溶膠及一陽離子界面活性劑，該陽離子界面活性劑包含四級銨鹽；(b)將該溶膠及該陽離子界面活性劑共縮合以形成一膠體；(c)提供一不織布基材，其在1kPa的一壓力下具有至少70%的一厚度留存比率；(d)將該不織布基材浸漬於該膠體中；及(e)在大氣壓力下加熱及乾燥以該膠體浸漬的該不織布基材以形成該絕熱材料，該絕熱材料具有經接合至該不織布基材上的一乾凝膠，其中該不織布基材在該絕熱材料中之含量按重量百分比係20%至96.7%，該乾凝膠在該絕熱材料中之含量按重量百分比係3%至60%，且該陽離子界面活性劑在該絕熱材料中之含量按重量百分比係0.3%至20%。
本揭露之實施例中進一步提供一種由前述絕熱材料製備的產品。
隨附圖式係用以提供對本揭露之實施例的進一步瞭解，並構成本說明書的一部分，且用以與本揭露的實施例一起解釋本揭露，但並未對本揭露加諸限制。藉由參照隨附圖式而描述詳細的實例實施例，所屬技術領域中具有通常知識者將變得更明白上述特徵、其他特徵、及優點，其中：
〔圖1〕係在本揭露之一實施例中製備之絕熱材料的照片。
為了使所屬技術領域中具有通常知識者能夠更佳地瞭解本揭露之實施例之技術解決方案，將在下文參照隨附圖式詳細地描述絕熱材料、製備絕熱材料之方法、及由本揭露之實施例中所提供的絕熱材料製備的產品。
其後將參照隨附圖式適當地描述本揭露之實施例，但所說明的實施例可以不同形式體現，且本揭露之實施例不應推斷為受限於本揭露所提出的實施例。反而，提供這些實施例之目的係欲使本揭露深入且完整，且欲使所屬技術領域中具有通常知識者能夠完全瞭解本揭露之範疇。
在無牴觸的情況下，本揭露的各實施例及實施例中的各特徵可彼此組合。
本揭露中所用之用語僅用以描述特定實施例，且並非意欲限制本揭露。如本揭露中所使用之用語「及/或(and/or)」包括一或複數個相關列表項目之任何及全部組合。如本揭露中所使用之
單數形式「一(a)」及「該(the)」亦意欲包括複數形式，除非上下文另有清楚指定。如本揭露中所使用之用語「包含(comprise)」及「由...製備(prepared from...)」指出所述特徵、整體、步驟、操作、組件、及/或總成的存在，但並未排除一或複數個其他特徵、整體、步驟、操作、組件、總成、及/或其等之群組的存在或添加。
除非另有定義，本揭露中所使用的所有用語(包括技術及科學用語)的意義與所屬技術領域中具有通常知識者通常瞭解者相同。亦將理解，那些用語(諸如常用字典中所定義者)應解譯為具有與相關技術及本揭露之背景中的意義一致的意義，且將不會解譯為具有理想化或過度正式的意義，除非在本揭露中如此明確地定義者。
除非另有定義，本申請案中之下列用語或描述具有下列意義：
「乾凝膠(Xerogel)」係用以描述藉由使膠體乾燥而形成之多孔固體的最終產品。
「溶膠(Sol)」係指用以形成膠體的原料。
「膠體(gel)」係指藉由膠接及共縮合溶膠所形成之膠態物質；在本申請案中，在形成乾凝膠之前，溶膠及膠體兩者均用以描述膠體。
「有機矽氧化物前驅物(Organosilicon oxide precursor)」係指當經水解及共縮合時形成有機矽氧化物的材料。
「初始厚度(Initial thickness)」係指在0.02kPa之壓力下所測量之不織布基材的平均厚度。
「Gsm」意指克重，其意指每平方公尺的克數，亦即，每平方公尺的材料克重。
「Clo值」係評估材料之絕熱能力的參數，其實質上係熱阻值。該值越大，則絕熱能力越佳。當不活動或從事腦力工作(卡值處於209.2kJ/m2 π h)的人在溫度21℃、相對濕度小於50%、且風速不超過0.lm/s的環境中感覺舒適時，由其所穿戴之衣物的Clo值係定義為1。
「A至B(A to B/A-B)」的描述包括A的值、B的值、及大於A且小於B的任何值。
「A在B中之重量百分比(percentage by weight of A in B)」意指A是B的一部分，且係指將B之重量當作100%時A之重量之百分比。
本揭露之實施例中提供一種絕熱材料，其包括一不織布基材、一乾凝膠、及一陽離子界面活性劑，其中該陽離子界面活性劑係分散在該乾凝膠中，且該乾凝膠係均勻地分布在該不織布基材之表面上及孔洞中並接合至該不織布基材，使得該不織布基材可藉由該乾凝膠之眾多孔洞捕集空氣，以達成絕熱效應。
在一些實施例中，不織布基材之材料可選自聚酯纖維(諸如垂直搭接之100%聚酯纖維(垂直搭接之不織布聚酯))，其克重可係50至1240gsm，但並未受限於此。
此外，不織布基材的初始厚度較佳地係2至50mm，且在1kPa之壓力下的厚度留存比率係至少70%，也就是說，不織布基材在1kPa壓力下的厚度不應小於初始厚度的70%，使得所製備的最終絕熱材料具有特定的絕熱效應。
當然，亦可將其他人造纖維或天然纖維(諸如尼龍纖維、丙烯酸纖維、聚丙烯纖維、聚乳酸纖維、纖維素纖維、及其他纖維材料)用作本揭露之實施例中的不織布基材，並無限制僅使用聚酯纖維。
本揭露之實施例中的乾凝膠係藉由使膠體乾燥而形成，且用以製備膠體之溶膠可包括有機矽氧化物前驅物、溶劑、催化劑、及類似物之成分。在本揭露之實施例中，有機矽氧化物前驅物之有機矽包括例如烷基三烷氧基矽烷或二烷氧基矽烷之烷氧基矽烷，且烷基三烷氧基矽烷可選自甲基三甲氧基矽烷(MTMS)、乙烯基三甲氧基矽烷、及其組合，而二烷氧基矽烷可係二乙氧基矽烷、二甲氧基矽烷、或其一組合。
用以製備膠體之溶膠中的溶劑係選擇性地添加並可選自醇，其作為例證可係甲醇、乙醇、或其一組合，但並未受限於此。
催化劑包括酸性催化劑及鹼性催化劑。可將酸性催化劑添加至溶劑及有機矽氧化物前驅物，以便使用酸性催化劑促成共縮合程序之水解反應的早期階段，而鹼性催化劑係在酸性催化劑之後添加，以便加速縮合反應以形成膠體。在一些實施例中，酸性催
化劑可選地可選自草酸、鹽酸、或其一組合；且鹼性催化劑可選自氫氧化銨、脲、及其組合，但其等並未受限於此。
可用在本揭露之實施例中的溶膠配方係描述於例如Chem.Mater.2005，第17卷，第2807至2816頁(Dong等人)；Chem.Mater.2004，第16卷，第11期，第2041頁(Loy等人)；Chem.Mater.2006，第18卷，第541至546頁(Dong等人)；J.Colloid Interface Sci.2006，300，第179至285頁(Rao等人)；WO 2010080239 A2等，其等係以引用方式併入本文中。
本揭露之實施例中的乾凝膠進一步包括陽離子界面活性劑，其可係四級銨鹽界面活性劑，且較佳地可係包含鹵素鹽之四級銨鹽界面活性劑(例如，十六基三甲基溴化銨、十六基三甲基氯化銨、溴化苄烷銨、氯化苄烷銨、或其一組合)。添加界面活性劑可促成溶膠中的成分分散。在本揭露之實施例中，使用四級銨鹽界面活性劑可進一步有助於促成聚合反應、確保乾燥之後的乾凝膠結構、及實現乾凝膠之抗菌效應。
本揭露之實施例中之製備絕熱材料之方法大致上可包括提供界面活性劑及溶膠，該溶膠包括溶劑、有機矽氧化物前驅物、及酸性催化劑(其中溶劑係選擇性添加的成分)。在本揭露之實施例中，界面活性劑較佳地係包括四級銨鹵素鹽之陽離子界面活性劑，且陽離子界面活性劑係與溶膠成分均勻地混合，接著將混合物持續留置一段時間(例如24小時)，使得混合物可經受水解及縮合反應的早期階段，且之後添加鹼性催化劑以起始膠凝及共縮合反
應，以便使溶膠及陽離子界面活性劑共縮合以形成膠體，並將不織布基材浸漬在膠體中，使得膠體完全地分布在不織布基材之表面上及孔洞中，且以膠體浸漬的不織布基材隨後係在環境壓力(例如1大氣壓)下加熱及乾燥以得到本揭露之實施例之絕熱材料。在一些實施例中，膠體的乾燥條件係1大氣壓及110至150℃的溫度，但並未受限於此，也就是說，本揭露之實施例可在環境壓力下製備乾凝膠，而不必使用超臨界或次臨界條件或溶劑交換。
不織布基材在本揭露之實施例中所製備之絕熱材料中之含量按重量百分比係20%至96.7%，乾凝膠之含量按重量百分比係3%至60%，且陽離子界面活性劑之含量按重量百分比係0.3%至20%，且絕熱材料具有良好的絕熱性質、透氣性、及抗菌效應，並具有穩定結構。下列實例進一步說明本揭露之實施例。
本揭露之實施例中的絕熱材料之各種特徵的測試方法係如下文所述：
厚度測量
具有30cm*30cm之大小的不織布基材之厚度係在0.02kPa下由厚度測試器測量，且結果係初始厚度(T0)。在1kPa之壓力下所測量之不織布基材的厚度係壓縮厚度(T1)。
厚度留存比率
厚度留存比率=壓縮厚度(T1)/初始厚度(T0)*100%。
絕熱效應
該效應係由Clo值表示，並使用ASTMC518標準測試方法進行測試，並取用三個測試結果的平均值。
壓縮狀態下的絕熱效應
該效應係由欲測試的絕熱材料在1kPa壓力下經壓縮時所得到的Clo值表示。
透氣度
透氣性係使用如用於不織布織品之GB/T24218.15-2018中華人民共和國國家標準測試方法中所指定之透氣性判定方法進行測試，其中測試面積係20cm2，且壓力差係200Pa。
抗菌效應
抗菌效應係使用AATCC100標準測試方法進行測試，其中使用大腸桿菌、金黃色葡萄球菌、及白色念珠菌。若可在24小時內抑制99.0%或更多的細菌，則認為其具有抗菌效應。
乾凝膠穩定性
以視覺觀察絕熱材料在完成之後及當處於壓縮狀態下時乾凝膠是否脫落，以評估附接至不織布基材之乾凝膠的穩定性。
藉由將有機矽氧化物前驅物、溶劑、酸性催化劑、及陽離子界面活性劑均勻混合30分鐘，並接著將混合物留置1小時，且隨後添加鹼性催化劑並均勻地混合以起始膠凝及共縮合反應以形成膠體來製備實驗實例2及5至8以及比較例1至2及5至9中之膠體。藉由將有機矽氧化物前驅物、溶劑、酸性催化劑、及陽離子界面活性劑均勻混合20分鐘，並接著將混合物留置24小時，且隨後添加鹼性催化劑並均勻地混合以起始膠凝及共縮合反應，並將混合物留置24小時以形成膠體來製備實驗實例1中之膠體。藉由將有機矽氧化物前驅物、溶劑、酸性催化劑、水、及陽離子界面活性劑均勻混合30分鐘，且隨後添加鹼性催化劑並持續攪拌30分鐘以形成膠體來製備實驗實例3中之膠體。藉由將有機矽氧化物前驅物、
溶劑、酸性催化劑、及陽離子界面活性劑均勻混合30分鐘，且隨後添加鹼性催化劑並持續攪拌30分鐘以形成膠體來製備實驗實例4中之膠體。
絕熱材料係藉由浸沒不織布纖維的各群組於前述膠體中來製備。對不織布基材的大小及重量以及所用的膠體量並無限制。原理係不織布基材可以膠體完全浸漬並吸附膠體。在完成浸漬之後，帶有膠體的不織布基材係在5kg/m2的擠壓壓力下饋入壓輥中以控制膠體的最終負載，並接著以150℃在環境壓力(亦即，大約1大氣壓)下執行乾燥以得到最終絕熱材料，其中不織布基材、乾凝膠、及界面活性劑的比例係其等在最終製備的絕熱材料中之重量百分率。
從表4可看出，相較於比較例，本揭露的實施例在壓縮狀態下每單位的不織布基材具有較佳的絕熱效應。若將比較例5進一步與比較例7相比，可看出即使在比較例7中添加乾凝膠，且其中的四級銨鹽有助於產生抗菌效應，但其等無助於改善壓縮狀態下之絕熱材料的絕熱效應。因此，在本申請案中發現到，不織布基材的適當厚度留存比率可有助於改善絕熱材料之絕熱效應，其中不織布基材的厚度留存比率較佳地係大於70%。
若將實驗實例2進一步與比較例1相比或者將實驗實例5進一步與比較例6相比，可看出當乾凝膠缺少四級銨鹽成分或四級銨鹽的比例過低時，乾凝膠與基材的結合強度將受影響。因此，可看出添加四級銨鹽至乾凝膠可有助於強化乾凝膠與基材的接合強度。在本申請案中發現到，四級銨鹽的比例較佳地係0.3%至20%。
從實驗實例2與比較例8及9之比較可看出，即使不織布基材具有適當的厚度留存比率及四級銨鹽比例，若不織布基材
比例及乾凝膠比例超過一範圍，則乾凝膠可脫落。也就是說，在本申請案中發現到，不織布基材的比例較佳地係20%至96.7%，且乾凝膠之比例較佳地係3%至60%。
此外，可從實驗實例與比較例的比較看出，添加四級銨鹽不僅有助於改善絕熱材料之結構穩定性，且亦使絕熱材料能夠產生抗菌效應。亦可從實驗實例2及比較例1看出，由本揭露之實施例之方法所提供的絕熱材料具有較佳的透氣性；且若比較具有類似克重的群組(實驗實例1及比較例3、實驗實例3及比較例4、以及實驗實例4及比較例5)，可看出由本揭露之實施例之方法所製備的絕熱材料具有優越的透氣性，且以適當比例添加四級銨鹽亦有助於改善絕熱材料的透氣性(實驗實例2與比較例1相比)。
因此，可看出本揭露之實施例中提供可在環境壓力下製備之具有良好結構穩定性、良好透氣性、及抗菌效應的絕熱材料，且該絕熱材料在經壓縮時維持良好絕熱能力，且因此適於應用至各種產品(諸如服裝、寢具、鞋類等)。由於本揭露之實施例的絕熱材料具有良好透氣性及抑菌能力，且在壓縮狀態下仍具有絕熱能力，當應用至鞋類、襪類、及其他產品時，絕熱材料可因而避免產生使人厭惡的氣味並允許使用者舒適及溫暖。
本揭露已揭示實例實施例，且雖然使用特定用語，其等係意欲且僅應解譯為具有通用性描述意義，且非意欲用於限制目的。在一些實例中，對所屬技術領域中具有通常知識者將係顯而易見的是，除非另有明確指示，連同特定實施例所述之特徵、特性、
及/或元件可單獨使用，或者可與連同其他實施例所述之特徵、特性、及/或組件組合使用。因此，所屬技術領域中具有通常知識者將瞭解，可在不偏離如附加申請專利範圍所提出之本揭露之範疇的情況下作出形式及細節的各種變化。
Claims (25)
- 一種絕熱材料，其包含：一不織布基材，其在1kPa的一壓力下具有至少70%的一厚度留存比率；一乾凝膠；及一陽離子界面活性劑，其包含四級銨鹽，並均勻地分散在該乾凝膠中；其中該不織布基材在該絕熱材料中之含量按重量百分比係20%至96.7%，該乾凝膠在該絕熱材料中之含量按重量百分比係3%至60%，且該陽離子界面活性劑在該絕熱材料中之含量按重量百分比係0.3%至20%。
- 如請求項1之絕熱材料，其中該不織布基材之材料係選自一聚酯纖維、一尼龍纖維、一丙烯酸纖維、一聚丙烯纖維、一聚乳酸纖維、及一纖維素纖維中之至少一者。
- 如請求項1之絕熱材料，其中該不織布基材在0.02kPa之一壓力下的一初始厚度係2mm至50mm。
- 如請求項1之絕熱材料，其中該乾凝膠係由包含一有機矽氧化物前驅物的一膠體形成，且該有機矽包含烷氧基矽烷。
- 如請求項4之絕熱材料，其中該烷氧基矽烷包含烷基三烷氧 基矽烷，且該烷基三烷氧基矽烷係甲基三甲氧基矽烷、乙烯基三甲氧基矽烷、及其組合。
- 如請求項4之絕熱材料，其中該烷氧基矽烷包含二烷氧基矽烷，且該二烷氧基矽烷係選自二乙氧基矽烷、二甲氧基矽烷、及其組合。
- 如請求項4之絕熱材料，其中該膠體進一步包含一溶劑及一催化劑。
- 如請求項7之絕熱材料，其中該溶劑包含醇，且該醇係選自甲醇、乙醇、及其組合。
- 如請求項7之絕熱材料，其中該催化劑包含一酸性催化劑及一鹼性催化劑。
- 如請求項9之絕熱材料，其中該酸性催化劑係選自草酸、鹽酸、及其組合。
- 如請求項9之絕熱材料，其中該鹼性催化劑係選自氫氧化銨、脲、及其組合。
- 如請求項1之絕熱材料，其中該陽離子界面活性劑之該四級銨鹽係選自四級銨鹵素鹽。
- 如請求項12之絕熱材料，其中該四級銨鹵素鹽係選自十六基三甲基溴化銨、十六基三甲基氯化銨、溴化苄烷銨、氯化苄烷銨、及其組合。
- 一種製備絕熱材料之方法，其包含：(a)提供一溶膠及一陽離子界面活性劑，該陽離子界面活性劑包含四級銨鹽；(b)將該溶膠及該陽離子界面活性劑共縮合以形成一膠體；(c)提供一不織布基材，其在1kPa的一壓力下具有至少70%的一厚度留存比率；(d)將該不織布基材浸漬於該膠體中；及(e)在大氣壓力下加熱及乾燥經該膠體浸漬的該不織布基材以形成該絕熱材料，該絕熱材料具有經接合至該不織布基材上的一乾凝膠，其中該不織布基材在該絕熱材料中之含量按重量百分比係20%至96.7%，該乾凝膠在該絕熱材料中之含量按重量百分比係3%至60%，且該陽離子界面活性劑在該絕熱材料中之含量按重量百分比係0.3%至20%。
- 如請求項14之製備絕熱材料之方法，其中該溶膠包含一有機矽氧化物前驅物，且該有機矽包含烷氧基矽烷。
- 如請求項15之製備絕熱材料之方法，其中該烷氧基矽烷包含 烷基三烷氧基矽烷，且該烷基三烷氧基矽烷係甲基三甲氧基矽烷、乙烯基三甲氧基矽烷、及其組合。
- 如請求項15之製備絕熱材料之方法，其中該烷氧基矽烷包含二烷氧基矽烷，且該二烷氧基矽烷係選自二乙氧基矽烷、二甲氧基矽烷、及其組合。
- 如請求項14之製備絕熱材料之方法，其中該四級銨鹽係選自四級銨鹵素鹽。
- 如請求項18之製備絕熱材料之方法，其中該四級銨鹵素鹽係選自十六基三甲基溴化銨、十六基三甲基氯化銨、溴化苄烷銨、氯化苄烷銨、及其組合。
- 如請求項14之製備絕熱材料之方法，其中該溶膠進一步包含一溶劑及一催化劑。
- 如請求項20之製備絕熱材料之方法，其中該溶劑包含醇，且該醇係選自甲醇、乙醇、及其組合。
- 如請求項20之製備絕熱材料之方法，其中該催化劑包含一酸性催化劑及一鹼性催化劑。
- 如請求項14之製備絕熱材料之方法，其中該不織布基材之材 料係選自一聚酯纖維、一尼龍纖維、一丙烯酸纖維、一聚丙烯纖維、一聚乳酸纖維、及一纖維素纖維中之至少一者，且該不織布基材在0.02kPa的一壓力下之一初始厚度係2mm至50mm。
- 如請求項14之製備絕熱材料之方法，其中步驟(e)中之該加熱條件係110℃至150℃。
- 一種由如請求項1至13中任一項之絕熱材料製備的產品。
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| CN102964111A (zh) | 2012-10-27 | 2013-03-13 | 山西天一纳米材料科技有限公司 | 以甲基三甲氧基硅烷为硅源制备保温隔热板的方法 |
| CA2920380C (en) * | 2013-08-09 | 2022-05-03 | Saint-Gobain Isover | Mineral fiber batting for the manufacture of thermally insulating composite |
| JP6738990B2 (ja) | 2014-08-26 | 2020-08-12 | パナソニックＩｐマネジメント株式会社 | 断熱シートおよびその製造方法 |
| CN107074563A (zh) * | 2014-09-25 | 2017-08-18 | 日立化成株式会社 | 气凝胶复合体、带有气凝胶复合体的支撑构件以及绝热材 |
| WO2016171558A1 (en) * | 2015-04-24 | 2016-10-27 | Separex S.A.S. | A process of applying a polymethylsilsesquioxane aerogel coating onto a porous substrate |
| WO2017010551A1 (ja) * | 2015-07-15 | 2017-01-19 | 日立化成株式会社 | エアロゲル複合材料 |
| JP7005490B2 (ja) | 2015-11-17 | 2022-01-21 | プリマロフト，インコーポレイテッド | エアロゲル及びポリマー材料を含有する合成繊維並びにそれの製造方法及びそれを含む物品 |
| CN105698488A (zh) * | 2016-01-29 | 2016-06-22 | 卓达新材料科技集团有限公司 | 一种无纺布/硅铝气凝胶复合保温板的常压干燥方法 |
| JP2019031994A (ja) * | 2017-08-04 | 2019-02-28 | 株式会社サムスン日本研究所 | 断熱材の製造方法、および複合断熱材 |
| CN109516763B (zh) * | 2019-01-07 | 2021-07-20 | 东华大学 | 一种纤维素纤维/SiO2复合气凝胶材料及其制备和应用 |
-
2020
- 2020-07-17 CN CN202010690351.5A patent/CN111893649B/zh active Active
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2021
- 2021-07-16 WO PCT/IB2021/056470 patent/WO2022013841A1/en active Application Filing
- 2021-07-16 TW TW110126242A patent/TW202206664A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2022013841A1 (en) | 2022-01-20 |
| CN111893649B (zh) | 2022-07-26 |
| CN111893649A (zh) | 2020-11-06 |
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