RESUMO
Peroxides are widely used as crosslinkers in polyethylene (PE) drinking water pipes. Cross-linked polyethylene (PEX) has better mechanical properties than PE, but peroxide decomposition by-products can migrate from PEX water pipes into the drinking water unless sufficient preventive actions are undertaken. This work systematically examines the migration of tert-Butyl methyl ether (MTBE), a dominating crosslinking by-product from PEX water pipes, into tap water by utilizing both experimental techniques and finite element (FEM) diffusion modeling. The effects of pipe geometry, tap water temperature (23-80⯰C), boundary conditions (air or water interface) and degasing (at 180⯰C) were considered. The MTBE diffusivity increased strongly with increasing temperature and it was concluded that a desired water quality can be achieved with proper degasing of the PEX pipes. As the FEM simulations were in excellent agreement with the experimental results, the model can accurately predict the MTBE concentration as a function of time, water temperature and PEX pipe geometry, and enable the pipe manufacturers to aid in ensuring desirable drinking water quality.
Assuntos
Éteres Metílicos , Poluentes Químicos da Água , Difusão , Peso Molecular , Polietileno , Qualidade da Água , Abastecimento de ÁguaRESUMO
Microbial fuel cells (MFCs) are emerging technology for wastewater treatment by chemical oxygen demand (COD) reduction and simultaneous bioelectricity production. Fabrication of an effective proton exchange membrane (PEM) is a vital component for MFC performance. In this work, green chitosan-based (CS) PEMs were fabricated with graphene oxide (GO) as filler material (CS-GO) and cross-linked with phosphoric acid (CS-GO-P(24)) or sulfuric acid (CS-GO-S(24)) to determine their effect on PEM properties. Interrogation of the physicochemical, thermal, and mechanical properties of the cross-linked CS-GO PEMs demonstrated that ionic cross-linking based on the incorporation of PO43- groups in the CS-GO mixed-matrix composites, when compared with sulfuric acid cross-linking commonly used in proton exchange membrane fuel cell (PEMFC) studies, generated additional density of ionic cluster domains, rendered enhanced sorption properties, and augmented the thermal and mechanical stability of the composite structure. Consequently, bioelectricity performance analysis in MFC application showed that CS-GO-P(24) membrane produced 135% higher power density than the CS-GO-S(24) MFC system. Simultaneously, 89.52% COD removal of primary clarifier municipal wastewater was achieved in the MFC operated with the CS-GO-P(24) membrane.
Assuntos
Fontes de Energia Bioelétrica , Águas Residuárias/química , Quitosana , Grafite , ÓxidosRESUMO
The effects of plasticization and cross-linking on the performance of chitosan as promising proton exchange membranes (PEMs) for bioelectricity generation in microbial fuel cells (MFCs) were investigated. The physico-chemical properties of chitosan (CS), sorbitol-chitosan (S-CS), phosphorylated-chitosan (CS-P) and phosphorylated-sorbitol-chitosan (S-CS-P) membranes were investigated by FESEM-EDS, FTIR-ATR, XRD, TGA, tensile strength and sorption studies. The performance of the fabricated PEMs was assessed by power density and cation exchange capacity (CEC). Maximum power densities achieved were 130.03, 20.76, 94.59 and 7.42mW/m(2) for CS-P, S-CS-P, S-CS and CS membranes respectively. Phosphorylation of the CS membranes increased CEC and tensile strength, attributed to an increase in bonded amide and phosphate ionic surface groups. Further, 49.07% COD removal from municipal wastewater was achieved with CS-P membranes. Thus, through chemical modifications, the physico-chemical and mechanical properties of natural abundant biopolymer chitosan can be enhanced for its use as an environmentally sustainable PEM in MFC technology.