功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
9期
9027-9032
,共6页
王海花%何凤%费贵强%牟静
王海花%何鳳%費貴彊%牟靜
왕해화%하봉%비귀강%모정
水性磺酸盐聚氨酯%聚吡咯%微观结构%成膜机理%相行为
水性磺痠鹽聚氨酯%聚吡咯%微觀結構%成膜機理%相行為
수성광산염취안지%취필각%미관결구%성막궤리%상행위
waterborne sulfonate polyurethane%polypyrrole%microstructure%film-forming mechanism%phase be-havior
以2,4-二氨基苯磺酸钠为亲水扩链剂,通过预聚体法合成了水性磺酸盐型聚氨酯分散液(SW-PU).并在FeCl3氧化剂的作用下,采用原位化学氧化聚合法制备了系列不同聚吡咯(PPy)质量浓度的水性聚氨酯/聚吡咯(SWPU/PPy)分散液,并通过溶液浇铸法制得系列复合导电薄膜.随着 PPy 的引入, SWPU分子与 PPy 分子间发生反应,SWPU/PPy 的高温热稳定性亦得到提高.随着吡咯质量浓度的增加,SWPU/PPy乳胶粒的粒径增加.经适量PPy改性后,PPy可在SWPU 胶束内部和表面均匀分布,形成大小均匀的纳米复合粒子;SWPU/PPy复合膜表面粗糙度下降,SWPU与PPy间具有较好的相容性.但当PPy质量浓度高于15%时,开始呈现一定的颗粒形貌,且薄膜表面粗糙度随着 PPy 浓度的增加明显增加;当PPy质量浓度高于30%时,胶膜表面颗粒形貌明显,胶膜表面主要由 PPy 组成.复合薄膜的渗透阈值介于质量浓度为1.5%~2%之间,当Py质量浓度为30%时,电导率高达1 S/cm.
以2,4-二氨基苯磺痠鈉為親水擴鏈劑,通過預聚體法閤成瞭水性磺痠鹽型聚氨酯分散液(SW-PU).併在FeCl3氧化劑的作用下,採用原位化學氧化聚閤法製備瞭繫列不同聚吡咯(PPy)質量濃度的水性聚氨酯/聚吡咯(SWPU/PPy)分散液,併通過溶液澆鑄法製得繫列複閤導電薄膜.隨著 PPy 的引入, SWPU分子與 PPy 分子間髮生反應,SWPU/PPy 的高溫熱穩定性亦得到提高.隨著吡咯質量濃度的增加,SWPU/PPy乳膠粒的粒徑增加.經適量PPy改性後,PPy可在SWPU 膠束內部和錶麵均勻分佈,形成大小均勻的納米複閤粒子;SWPU/PPy複閤膜錶麵粗糙度下降,SWPU與PPy間具有較好的相容性.但噹PPy質量濃度高于15%時,開始呈現一定的顆粒形貌,且薄膜錶麵粗糙度隨著 PPy 濃度的增加明顯增加;噹PPy質量濃度高于30%時,膠膜錶麵顆粒形貌明顯,膠膜錶麵主要由 PPy 組成.複閤薄膜的滲透閾值介于質量濃度為1.5%~2%之間,噹Py質量濃度為30%時,電導率高達1 S/cm.
이2,4-이안기분광산납위친수확련제,통과예취체법합성료수성광산염형취안지분산액(SW-PU).병재FeCl3양화제적작용하,채용원위화학양화취합법제비료계렬불동취필각(PPy)질량농도적수성취안지/취필각(SWPU/PPy)분산액,병통과용액요주법제득계렬복합도전박막.수착 PPy 적인입, SWPU분자여 PPy 분자간발생반응,SWPU/PPy 적고온열은정성역득도제고.수착필각질량농도적증가,SWPU/PPy유효립적립경증가.경괄량PPy개성후,PPy가재SWPU 효속내부화표면균균분포,형성대소균균적납미복합입자;SWPU/PPy복합막표면조조도하강,SWPU여PPy간구유교호적상용성.단당PPy질량농도고우15%시,개시정현일정적과립형모,차박막표면조조도수착 PPy 농도적증가명현증가;당PPy질량농도고우30%시,효막표면과립형모명현,효막표면주요유 PPy 조성.복합박막적삼투역치개우질량농도위1.5%~2%지간,당Py질량농도위30%시,전도솔고체1 S/cm.
Waterborne sulfonate polyurethane dispersion (SWPU ) was prepared through prepolymerization method with 2,4-diamino-benzene sulfonic acid sodium salt (DASS)as hydrophilic chain extender.Then with the assistant of FeCl3 oxidant,SWPU/polypyrrole (SWPU/PPy)dispersions with different mass concentration of polypyrrole (PPy)were prepared by in situ chemical oxidative polymerization,and the corresponding conduc-tive composite films were obtained by solution casting method.With the introduction of PPy,new urea bond was formed through the reaction between SWPU and PPy.The high-temperature thermal stability was also im-proved.With the increase of pyrrole content,the average particle size of SWPU/PPy dispersions increased.Sig-nificant aggregation was detected among SWPU colloidal particles,and the SWPU/PPy particles disperse well. With the addition of certain amount of PPy,PPy was able to distribute uniformly across SWPU colloidal parti-cles,and homogeneous nanocomposites were therefore formed;in addition,the surface roughness decreased, and good compatibility between SWPU and PPy was detected.However,particular morphology appeared when the mass concentration of PPy was higher than 1 5%,and surface roughness increased with increasing the mass concentration of PPy.Particular morphology became apparent when the mass concentration of PPy was 30%, the surface of SWPU/PPy was mainly composed of PPy.The percolation threshold of SWPU/PPy films was in the range of 1.5%-2%,and the surface conductivity reached 1 S/cm when PPy content was 30%.