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Synthesis and characterization of polymers and interpenetrating polymer networks (IPNs) with nonlinear optical (NLO) properties and related numerical studies.

机译:具有非线性光学(NLO)特性的聚合物和互穿聚合物网络(IPN)的合成和表征以及相关的数值研究。

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摘要

Copolymers of methyl methacrylate (MMA) and 2-propenoic acid, 2-methyl-, 2-[[[[4-methyl-3-[[[2-methyl-4-nitrophenyl)amino]carbonyl]aminophenyl]carbonyl]oxy]ethyl ester (PAMEE) exhibiting nonlinear optical (NLO) properties have been synthesized. Two kinds of urethane containing interpenetrating polymer networks (IPNs), consisting of nonlinear optical (NLO) chromophore, 2-methyl-4-nitroaniline (MNA) or Disperse Red1 (DR1) have been synthesized. The IPN systems consist of either aliphatic polycarbonate urethane (PCU) or 2,6-dimethyl-1,4-phenylene oxide (PPO) as one network and crosslinked poly (MMA-co-PAMEE) or poly (MMA-co-PMNEE) as the second network. Copolymers and interpenetrating polymer networks (IPNs) were characterized by IR spectroscopy, UV-VIS spectroscopy, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and second harmonic generation (SHG) measurements. The thin films of copolymers and IPNs were optically transparent and the corona poled polymers produced relatively large and stable SHG signals at room temperature.; To understand the polarization decay of our NLO polymer we studied a simple theoretical model which can account for the main features which we observe. The addition of an apparent "chemical" reaction with a reaction activation energy EAB to the neighbor-facilitated Fredrickson-Anderson model shows the existence of a beta relaxation occurring simultaneously with the main alpha process. The combination of an Ising-model with antiferromagnetic interaction and the neighbor-facilitated Fredrickson-Anderson model allows a description of the polarization decay of polarized materials, such as our polymers, below the glass transition temperature Tg. The relaxation time for the polarization scales with the relaxation time of the alpha-process of the glass transition, and shows a typical curvature in the ln tau versus T-1 plot. Real polymers, such as poly(MMA-co-PAMEE) which we study possess both of these features and its experimental average dipolar orientation matches closely with the theoretical average dipolar orientation below the glass transition temperature.
机译:甲基丙烯酸甲酯(MMA)和2-丙烯酸,2-甲基-,2-[[[[[4-甲基-3-[[[2-甲基-4-硝基苯基)氨基]羰基]氨基苯基]羰基]氧基的共聚物已经合成了表现出非线性光学(NLO)性质的对乙基酯(PAMEE)。合成了两种含氨基甲酸酯的互穿聚合物网络(IPN),它们由非线性光学(NLO)生色团,2-甲基-4-硝基苯胺(MNA)或分散红1(DR1)组成。 IPN系统由作为一个网络的脂肪族聚碳酸酯氨基甲酸酯(PCU)或2,6-二甲基-1,4-苯撑环氧乙烷(PPO)和交联的聚(MMA-co-PAMEE)或聚(MMA-co-PMNEE)组成作为第二个网络。通过红外光谱,紫外可见光谱,差示扫描量热法(DSC),扫描电子显微镜(SEM)和二次谐波产生(SHG)测量来表征共聚物和互穿聚合物网络(IPN)。共聚物和IPN的薄膜是光学透明的,电晕极化的聚合物在室温下产生相对较大且稳定的SHG信号。为了了解我们的NLO聚合物的极化衰减,我们研究了一个简单的理论模型,该模型可以解释我们观察到的主要特征。将具有反应活化能EAB的表观“化学”反应添加到邻居促进的Fredrickson-Anderson模型中,表明存在与主要α过程同时发生的β弛豫。具有反铁磁相互作用的伊辛模型与邻居促进的弗雷德里克森-安德森模型的结合,可以描述在玻璃化转变温度Tg以下的极化材料(例如我们的聚合物)的极化衰减。偏振的弛豫时间与玻璃化转变的α过程的弛豫时间成比例,并且在ln tau与T-1图中显示出典型的曲率。我们研究的真实聚合物,例如聚(MMA-co-PAMEE)具有这两个特征,并且其实验平均偶极子取向与玻璃化转变温度以下的理论平均偶极子取向紧密匹配。

著录项

  • 作者

    Sharma, P. R. Srikanth.;

  • 作者单位

    State University of New York at Albany.;

  • 授予单位 State University of New York at Albany.;
  • 学科 Chemistry Organic.; Chemistry Physical.; Chemistry Polymer.; Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 1998
  • 页码 156 p.
  • 总页数 156
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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