The effect of anionicity on mechanical degradation of polyacrylamide-type flocculants

被引:2
|
作者
Alizadeh, Hamid [1 ]
Pawlik, Marek [1 ]
机构
[1] Univ British Columbia, Norman B Keevil Inst Min Engn, 517-6350 Stores Rd, Vancouver, BC V6T 1Z4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Polyacrylamide; Molecular weight distribution; Intrinsic viscosity; Flexibility; Molecular weight; Size exclusion chromatography; Flocculants; ULTRASONIC DEGRADATION; POLYMER-SOLUTIONS; FLOC STRENGTH; DILUTE; MACROMOLECULES; TEMPERATURE; POLYSTYRENE; VISCOSITY; LIGHT;
D O I
10.1016/j.polymdegradstab.2024.110745
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The effect of ultrasonication, screening and shearing on five polyacrylamide-based flocculants of similar molecular weight but different degrees of anionicity (DA) was studied through measurement of intrinsic viscosity ([i]) and size exclusion chromatography (SEC) to investigate the influence of DA on the degradation of polymers. It was found that screening did not affect the [i] of the polymers while the effect of shearing was most noticeable in the cases of non-ionic and most anionic flocculants. Furthermore, ultrasonication caused a sharp decrease in the [i] which indicates a rapid degradation of the polymers. The results suggested that degradation of the polymers as a result of ultrasonication was irreversible since after a 24 hour resting period, the [i] did not recover to the values obtained for the untreated samples. Using a ratio of the [i] in distilled water to that in a dilute electrolyte as a measure of the relative flexibility of the flocculant chain, it was shown that the most flexible flocculants resisted ultrasonication and degradation better than those with rigid chains. Results from SEC confirmed that the degradation of polymers due to ultrasonication was a result of breakage of the polymer chains into sections of lower molecular weights.
引用
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页数:10
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