Coupled catalytic dephosphorylation and complex phosphate ion-exchange in networked hierarchical lanthanum carbonate grafted asymmetric bio-composite membrane

• Published in: Journal of colloid and interface science 2022-01, Vol.606, p.2024-2037
• Main Authors: Srivastava, Anup K., Kaundal, Babita, Sardoiwala, Mohammed Nadim, Choudhury, Subhasree Roy, Karmakar, Surajit
• Format: Article
• Language: English
• Subjects: Casein nanoparticles; Catalytic dephosphorylation; Ion-exchange mechanism; Lanthanum carbonate; Phosphate recovery; Remediation
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2021.09.173

[Display omitted] •Chemical crosslinking of mREM with CsNPs results in a robust bio-composite (REMC) membrane.•REMC inherit co-functionality of the active catalytic dephosphorylation and ion exchange-based separation of non-reactive phosphates.•Homogeneity in lanthanum ion distributed on REMC surface catalyzes non-enzymatic dephosphorylation of organic phosphate.•Liberated phosphate ions are trapped in REMC via complex ion (CO3– /PO43-) exchange process. The remediation of non-reactive phosphate pollutants in the aquatic system is essential for protecting the ecological niche. In this work, a highly robust protein nanoparticles networked rare-earth metal carbonate-grafted bio-composite membrane (abbreviated as REMC) was fabricated via chemical crosslinking of three-dimensional (3D) hierarchical lanthanum carbonate (mREM) and casein nanoparticles (CsNPs) for selective rejection of non-reactive phosphates. The main components of the REMC membrane are mREM and CsNPs, which were prepared via SDS/CTAB templated homogeneous precipitation and the coacervation/desolvation hybrid method, respectively. The active lanthanum ion (La3+) on the 3D spherulitic surface of mREM exhibited excellent phosphate adsorption capacity (maximum adsorption capacity was 358 mg.g−1) across a wide pH range and in a multi-ionic environment. A series of batch testing and characterizations revealed that the active La3+ and dominating phosphate centers in the REMC membrane framework enable non-enzymatic phosphatase-like activity, cleaving the phosphate ester bond of organic phosphates and releasing free phosphate anions. These released phosphate ions are retained in the REMC membrane via an ion exchange mechanism, where they contribute to improved phosphate removal capacities. Furthermore, CsNPs have a dual function in the membrane, acting as a matrix in the REMC membrane framework and contributing to phosphate ion sequestrations in a synergistic manner. The catalysis of para-nitrophenyl phosphates (pNPP) to paranitrophenol (pNP) in a sequential dephosphorylation by REMC offers an estimate of reaction kinetics and elucidates the underlying mechanism of improved phosphate selectivity in a multi-ionic environment. Furthermore, phosphate specificity, homogeneous binding capacity, reusability, and visual observation of REMC membrane saturation binding direct it's useful economic, industrial applications in aqueous phosphate contaminant removal, which could be beneficial for the active recovery