Solute clustering in undersaturated solutions - systematic dependence on time, temperature and concentration

• Published in: Physical chemistry chemical physics : PCCP 2018, Vol.2 (22), p.1555-15559
• Main Authors: Svärd, Michael, Renuka Devi, K, Khamar, Dikshitkumar, Mealey, Donal, Cheuk, Dominic, Zeglinski, Jacek, Rasmuson, Åke C
• Format: Article
• Language: English
• Subjects: Clustering; Infrared tracking; Molecular chains; Molecular dynamics; Particle size distribution; Photon correlation spectroscopy; Pore size; Porosity; Small angle X ray scattering; Temperature dependence; Time dependence
• ISSN: 1463-9076; 1463-9084; 1463-9084
• DOI: 10.1039/c8cp01509k

Molecular clustering and solvent-solute interactions in isopropanol solutions of fenoxycarb have been thoroughly and systematically investigated by dynamic light scattering, small-angle X-ray scattering, and nanoparticle tracking, supported by infrared spectroscopy and molecular dynamics simulations. The existence of molecular aggregates, clusters, ranging in size up to almost a micrometre is clearly recorded at undersaturated as well as supersaturated conditions by all three analysis techniques. The results systematically reveal that the cluster size increases with solute concentration and time at stagnant conditions. For most concentrations the time scale of cluster growth is of the order of days. In undersaturated solutions the size appears to eventually reach a maximum value, higher the higher the concentration. Below a certain concentration threshold clusters are significantly smaller. Clusters are found to be smaller in solutions pre-heated at a higher temperature, which offers a possible explanation for the so-called "history of solution" effect. The cluster distribution is influenced by filtration through membranes with a pore size of 0.1 μm, offering an alternative explanation for the "foreign particle-catalysed nucleation" effect. At moderate concentrations larger clusters appear to be sheared into smaller ones, but the original size distribution is rapidly re-established. At higher concentrations, although still well below solubility, the cluster size as well as solute concentration are strongly affected, suggesting that larger clusters contain at least a core of more organized molecules not able to pass through the filter. The appearance, growth and steady-state size distribution of clusters of organic molecules in solution depend on composition, temperature and pre-treatment.