Integrating eco-technological approach for textile dye effluent treatment and carbon dioxide capturing from unicellular microalga Chlorella vulgaris RDS03: a synergistic method.

A pilot-scale treatment method was used in the present study to test the biosorption of textile dye from textile effluent and carbon dioxide using Chlorella vulgaris RDS03. The textile dye effluent treatment achieved that textile dye biosorption capacity (qmax) rate of 98.84% on 15 days of treatment using Chlorella vulgaris RDS03. The Langmuir and Freundlich isotherm kinetics model indicated that the higher R2 value 0.98. The microalga Chlorella vulgaris RDS03 was captured-96.86% of CO2 analyzed by CO2 utilization and biofixation kinetics, 4.65 mgmL-1 of biomass, 189.26 mgg-1 of carbohydrate, 233.89 mgg-1 of lipid, 4.3 mLg-1 of bioethanol and 4.9 mLg-1 of biodiesel produced. We performed fatty acid methyl ester (FAME) profiling using gas chromatography-mass spectrometry (GCMS). We found 40 types of biodiesel compounds, specifically myristic acid, pentadecanoic acid, octadecanoic acid, palmitic acid, and oleic acid. The high-performance liquid chromatography (HPLC) validated and analyzed the produced bioethanol.Novelty of the Research• Unicellular microalga Chlorella vulgaris RDS03 was isolated from the freshwater region and investigated their biosorption efficiency against hazardous synthetic azo textile dyes.• Chlorella vulgaris RDS03 ability to biosorption 96.86% of environmental polluted carbon dioxide• Treated biomass was used to produce ecofriendly, unpolluted and green energy such as biofuels (biodiesel and bioethanol).

Electrochemical Investigation and Molecular Docking Techniques on the Interaction of Acridinedione Dyes with Water-Soluble Nonfluorophoric Simple Amino Acids.

Electrochemical studies of resorcinol-based acridinedione (AD) dyes with nonfluorophoric simple amino acids, glycine, alanine, and valine, were carried out in water. AD probes are classified into photoinduced electron transfer (PET) and non-PET-based dyes, wherein the electrochemical properties and photophysical and photochemical behavior vary significantly based on the nature of substituent groups and the nature of the solute. The oxidation potential of PET dye (ADR1) to that of non-PET-based dye (ADR2) differs significantly such that the addition of amino acids results in a shift of the oxidation peak to a less positive potential and the reduction peak to a lesser negative potential. The extent of shift of oxidation and reduction potential in PET dye is more pronounced than that of non-PET dye on the addition of valine rather than glycine. The variation in the shift is attributed to the presence of an electron-donating moiety (OCH3) group in the ninth position of ADR1 dye. Consequently, the quenching of fluorescence is observed in ADR2 with non fluorophoric amino acids that are authenticated by the shift of the anodic and cathodic peaks toward a lesser positive potential. Molecular docking (MD) studies of PET and non-PET dye with amino acids portray that neither hydrophobic interactions nor electrostatic or weak interactions such as van der Waals and pi-pi interactions govern the electrochemical nature of dye on the addition of amino acids. Furthermore, the formation of a conventional hydrogen bond between dye and amino acid is established from MD studies. The existence of dye-water-amino acid competitive hydrogen-bonding interactions is presumably well-oriented throughout the aqueous phase as observed through photophysical studies which support our electrochemical investigation.