Charge Regulation, Colloidal Stability and Adhesive Performance of Poly(vinyl alcohol)–Colloidal Silica Composites Modified with Guanidinium Polyacrylate Derived from Waste Guanidine Thiocyanate

Oston Qudratov

Bukhara State Technical University, Bukhara, Republic of Uzbekistan.

Bobir Olimov *

Bukhara State Technical University, Bukhara, Republic of Uzbekistan.

*Author to whom correspondence should be addressed.


Abstract

Aims: To establish how a guanidinium polyacrylate (GPA) modifier obtained from waste guanidine thiocyanate controls the charge state, colloidal stability, rheology and service properties of poly(vinyl alcohol) (PVA)–colloidal silica composite adhesives.

Study Design: Experimental study combined with colloid-chemical modelling (electrokinetics, ionic strength, DLVO and Stern–Langmuir analysis).

Place and Duration of Study: Department of Chemical Technology, Bukhara State Technical University, Uzbekistan, from 5 March 2024 to 15 September 2026.

Methodology: Composites were prepared with a basic formulation of 40 g GPA, 100 g of polymer matrix, 15 g of 30 % colloidal silica sol and 5 g of 37 % formalin; the GPA content was varied from 0 to 60 g and the sol content from 5 to 25 g. ζ-potential, hydrodynamic particle size, storage stability, rheological parameters, contact angles, work of adhesion, lap-shear adhesion strength, mechanical properties, water resistance and antibacterial activity were measured.

Results: Increasing the GPA content shifted the ζ-potential from −28.6 to +16.8 mV, with charge reversal between 30 and 40 g and a maximum particle size (128.5 nm) at 30 g. Stoichiometric neutralisation of the silica surface charge would require only 0.01–0.07 g GPA, whereas the practical formulations (20–60 g) have an ionic strength of 0.17–0.50 mol/kg and a Debye length below 1 nm; the DLVO barrier vanishes above about 100 mM, so stability is provided mainly by adsorbed PVA and hydration forces. At 15 g of sol, the composite had η = 950 mPa·s, n = 0.68, particle size 89.6 nm and a storage life of 120 days. Adhesion strength was 6.8, 5.2, 6.1 and 6.4 MPa on metal, wood, glass and ceramics (44.4–61.9 % above the unmodified reference), water uptake after 24 h was 1.8 % (7.6 % for the reference), and the inhibition zone of 18.4 mm retained 91.8 % after washing.

Conclusion: The GPA content and the silica-to-modifier ratio are the key variables that link the charge state of the dispersion with adhesion, water resistance and washing-resistant antibacterial activity; the basic formulation (40 g GPA and 15 g of 30 % sol per 100 g of matrix) provides the best compromise between these opposing requirements.

Keywords: Guanidinium polyacrylate, colloidal silica, zeta potential, charge reversal, DLVO theory, poly(vinyl alcohol) adhesive, antibacterial activity, waste valorisation


How to Cite

Qudratov, Oston, and Bobir Olimov. 2026. “Charge Regulation, Colloidal Stability and Adhesive Performance of Poly(vinyl alcohol)–Colloidal Silica Composites Modified With Guanidinium Polyacrylate Derived from Waste Guanidine Thiocyanate”. Chemical Science International Journal 35 (6):40-50. https://doi.org/10.9734/CSJI/2026/v35i61083.

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