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Development of light-responsive polymeric membranes for controlled caffeine delivery based on photochromic spiro-compounds

机译:开发用于基于光致变色螺环化合物控制咖啡因输送的光响应性聚合物膜

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摘要

Different approaches to obtain light-responsive membranes with the ability to switch their caffeine permeability resistance were developed in a copolymerization and in a postmodification process.udSynthesis of six photochromic methacrylic and acrylic spiropyrans and spirooxazines was successfully achieved. Copolymerization of these monomeric spiro-compounds resulted in photochromic materials. Additionally, a spiropyran with carboxylic acid functionality was synthesized. This enabled to postmodify non-photochromic polymeric materials with alcohols or amines on their surface to obtain photochromic materials.udThe first developed approach was to coat porous polymeric membranes with photochromic materials. Covalently linked coatings were achieved either by surface induced atom transfer random polymerization (ATRP) or by plasma activation of the membrane surface followed by random free radical polymerization. Copolymerization of spiro-compounds during the coating process as well as postmodification of preformed non-photochromic coatings with spiropyran resulted in photochromic membranes. UV-irradiation of such membranes resulted in a strong coloration of the membrane, in a reduction of surface tension and in a decreased caffeine permeability resistance.udPlasma activation resulted in thin coatings with thicknesses below 10 nm. Nevertheless it was possible to produce a membrane that reduced its caffeine permeability resistance of about 97% when the membrane was irradiated with UV-light compared to measurements at daylight.udThicknesses of ATRP-coatings were found to be depending on the polymerization time and the monomer concentration during the polymerization process. If too much coating was on the membrane, no caffeine permeability was any longer detectable. If there was not enough coating on the membrane, the caffeine permeability resistance was not switching. Therefore, an intermediate coating thickness turned out to be important for the production of useful photochromic membranes. Membranes produced with an ATRP-process lowered in the best case their permeability resistance of about 65% under UV-irradiation compared to measurements at daylight.udProduction of nonporous photochromic membranes was achieved by producing amphiphilic conetworks containing spiropyrans. UV-irradiation of such photochromic amphiphilic conetworks resulted in a red coloration and in a decreased caffeine permeability resistance. Changing the composition of the amphiphilic conetwork allowed tuning the basic caffeine permeability resistance. Copolymerization of spiropyran during the production of the amphiphilic conetwork resulted in a membrane that lowered its caffeine permeability resistance under UV-irradiation of around 43% compared to measurements at daylight. udCombination of porous membranes with amphiphilic conetworks was achieved in a grafting through process. The surface of a porous membrane was coated with acrylic units and the amphiphilic network was produced on that surface. This covalently linked amphiphilic conetwork resulted in an inversed permeability switch. The caffeine permeability resistance was about eight times higher under UV-irradiation than at daylight.udStability measurements under UV-irradiation showed that postmodified membranes had in general lower fading rates than copolymerized membranes.ud
机译:在共聚和后改性过程中,开发了获得具有切换其咖啡因渗透性的能力的光响应膜的不同方法。 ud成功地合成了六种光致变色甲基丙烯酸和丙烯酸螺吡喃和螺恶嗪。这些单体螺环化合物的共聚导致光致变色材料。另外,合成了具有羧酸官能团的螺吡喃。这样就可以在非光致变色聚合物材料的表面上用醇或胺进行后改性,以获得光致变色材料。 ud最早开发的方法是用光致变色材料涂覆多孔聚合物膜。共价连接的涂层可通过表面诱导的原子转移无规聚合(ATRP)或通过膜表面的等离子体活化,然后进行无规自由基聚合来实现。螺旋化合物在包衣过程中的共聚合以及预先形成的非光致变色涂层与螺吡喃的后改性导致光致变色膜。此类膜的紫外线照射导致该膜强烈着色,降低表面张力并降低了咖啡因渗透性。 ud等离子体活化导致厚度小于10 nm的薄涂层。然而,与白天进行测量相比,用紫外线照射该膜时,其咖啡因渗透性的耐受性可能会降低约97%。 ATDR涂层的厚度取决于聚合时间和聚合度。聚合过程中的单体浓度。如果膜上的涂层过多,则无法再检测到咖啡因的渗透性。如果膜上没有足够的涂层,则咖啡因渗透性的阻力不会改变。因此,中间涂层厚度被证明对于生产有用的光致变色膜很重要。在最佳情况下,采用ATRP工艺生产的膜在紫外线照射下的通透性比在白天进行测量时降低了约65%。 ud通过生产含有螺吡喃的两亲共网络可实现无孔光致变色膜的生产。这种光致变色两亲性共网络的紫外线照射导致红色,并且咖啡因渗透性抵抗力降低。改变两亲性网络的组成可以调节基本的咖啡因渗透性。与在白天进行测量相比,在两亲性共网络生产过程中螺吡喃的共聚导致膜在紫外线照射下的咖啡因渗透性降低了约43%。多孔膜与两亲共网络的结合是通过接枝过程实现的。多孔膜的表面涂有丙烯酸单元,并在该表面上形成了两亲网络。这种共价连接的两亲性共网络导致了反向渗透率转换。在紫外线照射下,咖啡因的渗透性比在日光下高约八倍。 ud在紫外线照射下的稳定性测量表明,后改性膜的褪色率通常低于共聚膜。

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    Baumann Lukas;

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  • 年度 2013
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  • 原文格式 PDF
  • 正文语种 {"code":"de","name":"German","id":7}
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