1983
DOI: 10.1016/0011-9164(83)80006-x
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Polypiperazinamides: new polymers useful for membrane processes

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Cited by 20 publications
(11 citation statements)
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“…The reduced presence of amidic hydrogen also improves the resistance to chlorine attack [63]. However, this membrane was not commercialised due to its relatively low salt rejection (≤ 95 %) [64]. The presence of the sulphonic and phenyl groups in sulfonated polysulfone was expected to enhance permeability, mechanical, chemical and biological stability however the salt rejection was below the acceptable level required to be commercialised [65].…”
Section: Challenges and Trends In Ro Desalination Technology Developmentmentioning
confidence: 99%
“…The reduced presence of amidic hydrogen also improves the resistance to chlorine attack [63]. However, this membrane was not commercialised due to its relatively low salt rejection (≤ 95 %) [64]. The presence of the sulphonic and phenyl groups in sulfonated polysulfone was expected to enhance permeability, mechanical, chemical and biological stability however the salt rejection was below the acceptable level required to be commercialised [65].…”
Section: Challenges and Trends In Ro Desalination Technology Developmentmentioning
confidence: 99%
“…However, the performance of the membranes was significantly affected by chlorine at pH of 7 and below. In order to improve chlorine resistance, integrally-skinned asymmetric membranes based on polypiperazinamides (PPA) were developed [217][218][219][220]. Despite their high chlorine resistance, PPA membranes were not commercialized due to unfavorable salt rejections [186].…”
Section: Integrally-skinned Asymmetric Membranesmentioning
confidence: 99%
“…The lack of solubility of poly(piperazinamides) has been attributed to the presence of a relatively rigid backbone and intermolecular dipole-dipole interactions in the polymers, similar to those of aramids. 3 Although hydrogen-bonded interactions are removed with incorporation of the piperazine ring, the rigidity of the polymer backbone in aromatic poly(piperazinamides) possibly remains relatively unchanged in comparison to aramids and, therefore, solubility is not improved because there is no accompanying increase in the flexibility of the polymer backbone. The piperazine ring is also expected to be in its chair conformation and, consequently, is not expected to interfere sterically with the resonance delocalization of the amide group (-NsCdO).…”
Section: Introductionmentioning
confidence: 99%