BackgroundThe interactions of microbes with metal ions form an important basis for our study of biotechnological applications. Despite the recent progress in studying some properties of Au(III) adsorption and reduction by Bacillus megatherium D01 biomass, there is still a need for additional data on the molecular mechanisms of biosorbents responsible for their interactions with Au(III) to have a further insight and to make a better exposition.ResultsThe biosorption mechanism of Au(III) onto the resting cell of Bacillus megatherium D01 biomass on a molecular level has been further studied here. The infrared (IR) spectroscopy on D01 biomass and that binding Au(III) demonstrates that the molecular recognition of and binding to Au(III) appear to occur mostly with oxygenous- and nitrogenous-active groups of polysaccharides and proteins in cell wall biopolymers, such as hydroxyl of saccharides, carboxylate anion of amino-acid residues (side-chains of polypeptide backbone), peptide bond (amide I and amide II bands), etc.; and that the active groups must serve as nucleation sites for Au(0) nuclei growth. A further investigation on the interactions of each of the soluble hydrolysates of D01, Bacillus licheniformis R08, Lactobacillus sp. strain A09 and waste Saccharomyces cerevisiae biomasses with Au(III) by IR spectrometry clearly reveals an essential biomacromolecule-characteristic that seems the binding of Au(III) to the oxygen of the peptide bond has caused a significant, molecular conformation-rearrangement in polypeptide backbones from β-pleated sheet to α-helices and/or β-turns of protein secondary structure; and that this changing appears to be accompanied by the occurrence, in the peptide bond, of much unbound -C=O and H-N- groups, being freed from the inter-molecular hydrogen-bonding of the β-pleated sheet and carried on the helical forms, as well as by the alternation in side chain steric positions of protein primary structure. This might be reasonably expected to result in higher-affinity interactions of peptide bond and side chains with Au(III).ConclusionsThe evidence suggests that the polypeptides appear to be activated by the intervention of Au(III) via the molecular reconformation and in turn react upon Au(III) actively and exert profound impacts on the course of Au(0) nucleation and crystal growth.
Background: Platinum nanomaterial is one of the significant noble metal catalysts, and the interaction of platinum with microbe is one of the key factors in influencing the size and the distribution of the platinum nanoparticles on the microbial biomass. Some properties of Pt(IV) adsorption and reduction by resting cells of Bacillus megatherium D01 biomass have once been investigated, still the mechanism active in the platinum biosorption remains to be seen and requires further elucidating.
Bisphenol A dicyanate (BADCy) resin nanoparticles were synthesized by precipitation polymerization and used to modulate the microstructure of the BADCy resin matrix. A microscopic mechanism model was used to characterize the curing process of BADCy resin systems with different contents of the prepared nanoparticles. Due to the curing process of the thermosetting resin being analogous to the crystallization process of the polymer, the Avrami equation was used to analyze the microscopic mechanism of the curing process. The reactive functional groups, structure, and size of the prepared BADCy resin nanoparticles were characterized by FT-IR, SEM, and TEM, respectively. The kinetic parameters of different systems were then obtained using the Avrami equation, and they adequately explained the microscopic mechanism of the curing process. The results showed that the Avrami equation effectively described the formation and growth of gel particles during the curing process of the BADCy resins. The addition of nanoparticles can affect the curing behavior and curing rate. Since the reaction between the BADCy resin nanoparticles and the matrix is dominant, the formation process of the gel particles was neglected. This phenomenon can be understood as the added BADCy resin nanoparticles replacing the formation of gel particles. The reasons for accelerated curing were analyzed from the perspective of thermodynamics and kinetics. Besides this, the Arrhenius equation for non-isothermal conditions correctly accounted for the change in the cross-linked mechanism in the late-stage curing process. A comparison of the theoretical prediction with the experimental data shows that the Avrami theory of phase change can simulate the curing kinetics of different BADCy resin systems well and explain the effects of BADCy resin nanoparticles on the formation of the microstructure.
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