𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Influence of pH and Humic Acid on Coagulation Kinetics of Kaolinite: A Dynamic Light Scattering Study

✍ Scribed by Ruben Kretzschmar; Helmut Holthoff; Hans Sticher


Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
196 KB
Volume
202
Category
Article
ISSN
0021-9797

No coin nor oath required. For personal study only.

✦ Synopsis


humic substances on surfaces of natural clays. Humic sub-Time-resolved dynamic light scattering was used to investigate stances are present in practically all surface-near soil and the influence of pH and adsorbed humic acid on the coagulation aquatic environments. They are negatively charged polykinetics of kaolinite clay colloids. Stability ratios, defined as the electrolytes of varying molecular weight and can strongly experimental fast coagulation rate divided by the coagulation rate sorb to surfaces of oxides and clay minerals. Adsorption of the sample under consideration, were determined from the iniof humic substances has been shown to increase negative tial increases in average hydrodynamic radius with time. Pure

surface charge and colloidal stability of iron oxide ( 10,11 ) kaolinite exhibited fast coagulation (stability ratio W Å 1) at all ionic strengths (0.001 to 1 M NaClO 4 ) when suspension pH was and clay colloids ( 5, 9 ) . In agreement with these studies, below 5.8. Above pH 5.8, coagulation rates were significantly reit has been shown that removal of adsorbed organic matter duced (W ú 1) and W exhibited pronounced ionic strength depenfrom natural soil clays reduces colloidal stability (6-8). dence. The observed behavior is explained by edge-to-face hetero-It has been speculated that a combination of electrostatic coagulation by electrostatic attractive forces at low pH and electroand steric stabilization is responsible for the increased colstatic stabilization at high pH. The transition in coagulation loidal stability of clay-humic complexes ( 6,8,9 ) . Howbehavior occurs at the point of zero charge (PZC) of the kaolinite ever, unequivocal evidence for steric stabilization of clay edge surfaces near pH 5.8. Small additions of humic acid at pH mineral colloids by adsorbed humic substances is lacking 4 resulted in edge charge reversal from positive to negative and and is difficult to obtain without direct measurements of substantially reduced coagulation rates (W ú 1); similar behavior was observed at pH 6. Relating the observed stability ratios W to coagulation kinetics (9).

zeta potentials suggests that at low to medium ionic strength Published studies on coagulation behavior of clay colloids (°0.01 M NaClO 4 ) the stabilizing effect of adsorbed humic acid are almost exclusively based on viscosity measurements usis purely electrostatic. However, at high ionic strength ( ¢0.1 M) ing concentrated suspensions (1, 3) or traditional sedimentasteric stabilization may also play a role. ᭧ 1998 Academic Press tion experiments with more dilute suspensions (2, 4-7, 9).


📜 SIMILAR VOLUMES


Effects of Cosolvents and pH on Protein
✍ Da Song; Daniel Forciniti 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 228 KB

Dynamic light scattering was used to study the adsorption of two proteins with different surface properties (IgG and HSA) on negatively charged polystyrene latex. The proteins were adsorbed from water and from water/methanol and water/glycerol mixtures at various pH. Some striking differences betwee

Gelation Studies on a Radical Chain Cros
✍ Sven Richter; Volodymyr Boyko; Klaus Schröter 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 134 KB

## Abstract **Summary:** The sol–gel transition of a radical chain cross‐linking copolymerization system [__N__‐vinylcaprolactam/2‐hydroxylethyl methacrylate/allyl methacrylate] has been studied using in situ time‐resolved dynamic light scattering (DLS) and in situ rheology. A critical dynamic beha