SYNTHESIS OF A NEW ORGANIC AEROGEL

WU Zhichao; ZHANG Zhicheng; ZHANG Manwei

Your Location：

Home >

Browse articles >

SYNTHESIS OF A NEW ORGANIC AEROGEL

Papers | Updated：2021-06-21

- SYNTHESIS OF A NEW ORGANIC AEROGEL
- SYNTHESIS OF A NEW ORGANIC AEROGEL
- 高分子科学（英文版） 1996年14卷第2期页码：127-133
- Affiliations：
  
  1.   Depart. of Appl. Chem.
  2.   University of Science and Technology of China
  3.   Hefei 230026
- Author bio：
- Funds：
- DOI：
  中图分类号： TQ427.6
- 纸质出版：1996-06-20
- Accepted：
Scan QR Code
[1]吴志超,张志成,张曼维.SYNTHESIS OF A NEW ORGANIC AEROGEL[J].Chinese Journal of Polymer Science,1996,{4}(02):127-133.

WU Zhichao, ZHANG Zhicheng, ZHANG Manwei. SYNTHESIS OF A NEW ORGANIC AEROGEL[J]. 1996, 14(2): 127-133.
[1]吴志超,张志成,张曼维.SYNTHESIS OF A NEW ORGANIC AEROGEL[J].Chinese Journal of Polymer Science,1996,{4}(02):127-133. DOI：

WU Zhichao, ZHANG Zhicheng, ZHANG Manwei. SYNTHESIS OF A NEW ORGANIC AEROGEL[J]. 1996, 14(2): 127-133. DOI：

摘要

正

A new organic aerogel made from （N- hydroxymethyl）-acrylamide （NA） and resorcinolis reported. The acidic solution of NA and resorcinol was irradiated by γ-rays with 1200-1800 Gy dose

then was heated to 60℃ for at least 16hr to form transparent sol-gel.The translucent aerogel can be obtained from the sol-gel with CO

as supercritical fluid.Synthetic conditions （e.g. acidity of the solution

ratio of NA to resorcinol） are discussed.

Abstract

A new organic aerogel made from （N- hydroxymethyl）-acrylamide （NA） and resorcinolis reported. The acidic solution of NA and resorcinol was irradiated by γ-rays with 1200-1800 Gy dose

then was heated to 60℃ for at least 16hr to form transparent sol-gel.The translucent aerogel can be obtained from the sol-gel with CO

as supercritical fluid.Synthetic conditions （e.g. acidity of the solution

ratio of NA to resorcinol） are discussed.

关键词

Keywords

references

浏览量

Downloads

CSCD

文章被引用时，请邮件提醒。

Submit

工具集

关联资源

Energy Storage Performance of Supercapacitors with Polyelectrolyte Surface Coatings: Effects of Dielectric Contrast

End-group and Side-chain Dual-engineering of Selenium-fused Acceptors for 20.08% Efficiency Polymer Solar Cells with Low Energy Loss

Advances in Polymer-based Circularly Polarized Luminescent Materials

Preparation and Chiral Recognition Ability of Crystalline Cellulose Phenylcarbamate

Improvements of Hydrophobicity and Toughness of Epoxy Coatings Modified with Hydroxyl-terminated Fluororubber