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Polymer electrolyte membrane (PEM) technologies hold promise for sustainable energy solutions, yet pinhole-related challenges persist. Our research introduces a novel biohybrid approach to self-healing, enhancing multiple healing cycles with minimal membrane disruption. Initial steps involve immobilizing enzymes on a polymeric membrane. This study establishes the immobilization process and analytical framework through enzyme immobilization on polypropylene. Applicability and stability are investigated, laying groundwork for potential Nafion™ applications and advancing climate neutral energy. Qualitative analysis employs colorimetric p-NPA assay on polypropylene-immobilized lipase from Candida rugosa (CRL) and Lipase B from Candida antarctica (CALB). Both enzymes hold their temperature optimum at 50°C which is increased by 10°C via immobilization. Diisopropylcarbodiimide (DIC) is optimal for immobilization. Synchronous enzyme and DIC addition is advantageous. After 8 reuse cycles, immobilized enzymes retain 54.3% residual activity. Immobilizates exposed to PEM fuel cell conditions show better stability due to covalent immobilization than free CRL. Yet, declines occur under stressors like 60 °C and concentrated alcohol. Immobilizates remain resilient at pH 3 and under oxidizing as well as reducing conditions constituted by varied gas atmospheres. Considering PEM fuel cells' operational range, in-depth investigations across conditions are vital. Future studies target long-term PEM fuel cell lifespans, focusing on extremophilic enzymes or modifications for high-temperature stability. Subsequently, the transferability of the immobilization method to Nafion™ shall be deliberated based on the outcomes.
Aljerf LoaiCorresponding author Department of Life Sciences, Faculty of Dentistry, University of Damascus
p-hydroxybenzoic acid esters are used as food and drug preservatives. These compounds were quantised by a reversed-phase thin-layer chromatography method based on the use of silanized silica gel as stationary phase. Thin layers chromatography of silanized silica gel (HF254) is implemented to separate p-hydroxybenzoic acid and its methyl, ethyl, propyl, butyl and benzyl esters. Borate buffer (pH 2) was used as a mobile phase with the addition of organic solvent as required. For the quantitative determination, the solutions to be analysed were applied in bands on 5 x 20 cm plates. The plates are developed in glass chromatography chambers lined with filter paper. After the plates have been developed they are dried at room temperature. The spots or bands of the various compounds are visualised under a 250-mµ UV light source. The extraction of the silica gel with methanol was effective. Six preservatives were separated with better results for benzyl- and butyl-p-hydroxybenzoates. Chromatographic development controlled by temperature stability in the chromatographic chamber and spectrophotometric determination of all the compounds were indicated. A second development with the same solvent mixture was suggested especially when low RF is involved. Various compounds are completely separated and a good determination of p-hydroxybenzoic acid and its principle esters are possible using a simple technique of elution and spectrophotometric determination.