Stabilization through precipitation in a system of colloidal iron(III) pyrophosphate salts

• Published in: Journal of colloid and interface science Vol. 381; no. 1; pp. 43 - 47
• Main Authors: van Leeuwen, Y. Mikal, Velikov, Krassimir P., Kegel, Willem K.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.09.2012; Elsevier
• Subjects: additives; Chemistry; Colloidal state and disperse state; Colloids; Diphosphates - chemistry; Exact sciences and technology; Ferric Compounds - chemistry; Flocculation; General and physical chemistry; Insoluble salt; Ionic strength; Iron - chemistry; Microscopy, Electron, Transmission; Nanoparticles; Nanoparticles - chemistry; Nanoparticles - ultrastructure; Osmolar Concentration; Physical and chemical studies. Granulometry. Electrokinetic phenomena; Precipitation; pyrophosphates; Salts; sediments; Solutions; Stabilization; Static Electricity; Nanoparticles; Precipitation; Stabilization; Ionic strength; Colloids; Insoluble salt; Stability; Nanoparticle; Sediments; Colloid; Dispersion; Aggregation; Additive; Iron III; Instability; Interaction potential; Aggregate
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2012.05.018

[Display omitted] ► The ionic strength decreases during the precipitation of an insoluble salt. ► The drop in ionic strength can be sufficient to stabilize a system during formation. ► We observe two stages in the aging of colloidal iron(III) pyrophosphate salts. ► While the nanoparticles are unstable, their aggregates remain in dispersion. ► Calculated interaction potentials confirm decreasing ionic strength as the cause. The ionic strength of a solution decreases during the precipitation of an insoluble salt, which can cause an initially unstable colloidal system to stabilize during its formation. We show this effect in the precipitation and aging of colloidal iron(III) pyrophosphate, where we observe two distinct stages in the aggregation process. The first stage is the formation of nanoparticles that immediately aggregate into clusters with sizes on the order of 200nm. In the second stage these clusters slowly grow in size but remain in dispersion for days, even months for dialyzed systems. Eventually these clusters become macroscopically large and sediment out of dispersion. Noting the clear instability of the nanoparticles, it is interesting to find two stages in their aggregation even without the use of additives such as surface active molecules. This is explained by accounting for the rapid decrease of ionic strength during precipitation, rendering the nanoparticles relatively stable when precipitation is complete. Calculating the interaction potentials for this scenario we find good agreement with the experimental observations. These results indicate that coupling of ionic strength to aggregation state can be significant and should be taken into account when considering colloidal stability of insoluble salts.