𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Gas Permeation Properties ofCopolyimides from1,4-Bis(3,4-dicarboxyphenoxy)benzeneDianhydride and 2,2-Bis(3,4-dicarboxyphenyl)hexafluoroisopropaneDianhydride

✍ Scribed by Li, Yuesheng; Ding, Mengxian; Xu, Jiping


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
330 KB
Volume
42
Category
Article
ISSN
0959-8103

No coin nor oath required. For personal study only.

✦ Synopsis


A series of aromatic copolyimides was prepared from 1,4-bis(3,4dicarboxyphenoxy)benzene dianhydride (HQDPA) and 2,2-bis(3,4-dicarboxyphenyl)hexaÑuoroisopropane dianhydride (6FDA) with 3,3@-dimethyl-4,4@-methylene dianiline (DMMDA) by a chemical imidization. The gas permeability coefficients of the copolyimides to and were measured under H 2 , CO 2 , O 2 , N 2 CH 4 7 atm. pressure. The fractional free volume of 6FDAÈDMMDA is larger than that of HQDPAÈDMMDA, while the chain segmental mobility of 6FDAÈ DMMDA is lower than that of HQDPAÈDMMDA. The gas permeability of 6FDAÈDMMDA is much higher than that of HQDPAÈDMMDA but the permselectivity of 6FDAÈDMMDA for over is lower than

CH 4 that of HQDPAÈDMMDA. The experimental values of the gas permeability coefficients of the copolyimides are in satisfactory agreement with the values estimated from the gas permeability coefficients of the constituent homopolyimides and their weight fractions.


📜 SIMILAR VOLUMES


Synthesis and properties of soluble arom
✍ Guey-Sheng Liou 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 152 KB 👁 1 views

Aromatic tetracarboxylic dianhydride having crank and twisted noncoplanar structure, 2,2 -bis(3,4-dicarboxyphenoxy)-1,1 -binaphthyl dianhydride, was synthesized by the reaction of 4-nitrophthalonitrile with 2,2 -dihydroxy-1,1 -binaphthyl, followed by alkaline hydrolysis of the intermediate bis(ether

Gas separation properties of aromatic po
✍ Yuesheng Li; Mengxian Ding; Jiping Xu 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 494 KB 👁 1 views

The gas transport properties of a series polyetherimides, which were prepared from 1,4his(3,4-dicarboxyphenoxy )benzene dianhydride (HQDPA) with l,3-phenylenediamine or 3,5-diaminobenzic acid (DBA) or its esters are reported. The effects of carboxylic group ( -COOH) and carboxylic ether groups ( -CO

Preparation and properties of soluble ar
✍ Dong-Ho Lee; Seung-Young Koo; Dae-Yong Kim; Heung-Jin Choi 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 190 KB 👁 2 views

Aromatic polyetherimides were synthesized from a fluorine containing aromatic carboxylic acid dianhydride, 2,2-bis [4-(3,4-dicarboxyphenoxy)phenyl]hexafluoropropane dianhydride (6F-BABPA) and five typical aromatic diamines including 1,1-bis(4-aminophenyl)-1-phenyl-2,2,2-trifluoroethane (3F-DAM) by t

Preparation and properties of novel solu
✍ Seung-Young Koo; Dong-Ho Lee; Heung-Jin Choi; Kil-Yeong Choi 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 556 KB

New aromatic polyetherimides containing the l,l'-bis[4-(3,4-dicarboxyphenoxy)phenyl] -1phenyl-2,2,2-trifluoroethane dianhydride unit were prepared by a conventional two-step method from l,l'-bis[4-(3,4-dicarboxyphenoxy)phenyl]-l-phenyl-2,2,2-trifluoroethane dianhydride and several diamines. This pro

Formation of honeycomb films based on a
✍ Xutong Han; Ye Tian; Lihua Wang; Changfa Xiao 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB 👁 2 views

## Abstract A soluble polyimide was synthesized from 2,2′‐bis[4‐(3,4‐dicarboxyphenoxy)phenyl]propane dianhydride (BPADA) and 3,3′‐dimethyl‐4,4′‐diaminodiphenylmethane (DMMDA) by a two‐step method, and it had good solubility both in strong bipolar solvents and in common low‐boiling‐point solvents. T

Preparation and properties of new solubl
✍ Guey-Sheng Liou; Masaki Maruyama; Masa-Aki Kakimoto; Yoshio Imai 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 145 KB 👁 1 views

A new aromatic tetracarboxylic dianhydride having a crank and twisted noncoplannar structure, 2,2Ј-bis(3,4-dicarboxyphenoxy)biphenyl dianhydride, was synthesized by the reaction of 4-nitrophthalonitrile with biphenyl-2,2Ј-diol, followed by hydrolysis and cyclodehydration. The biphenyl-2,2Ј-diyl-cont