Yen-Peng Ting

Silver Nanoplates: From Biological to Biomimetic Synthesis

This paper describes the synthesis of single-crystalline Ag nanoplates using the extract of unicellular green alga Chlorella vulgaris at room temperature. Proteins in the extract were involved in the biological synthesis, providing the dual function of Ag ion reduction and shape-controlled synthesis of nanosilver. Hydroxyl groups in Tyr residues and carboxyl groups in Asp and/or Glu residues were further identified as the most active functional groups for Ag ion reduction and for directing the anisotropic growth of Ag nanoplates, respectively. The kinetics of Ag ion reduction in biological systems was discussed and probed by using custom-designed peptides. The results showed the Tyr content (the reduction source) and the content of Ag complexers (the reaction inhibitors, e.g., His and Cys) in the protein molecules as important factors affecting the reduction kinetics. The comprehensive system identification effort has led to the design of a simple bifunctional tripeptide (DDY-OMe) with one Tyr residue as the reduction source and two carboxyl groups in the Asp residues as shape-directors, which could produce small Ag nanoplates with low polydispersivity in good yield (>55%). The roles of the carboxyl groups in the formation of Ag nanoplates were also discussed.

Biosorption of gold by immobilized fungal biomass

The characteristics of polyvinyl alcohol (PVA) and calcium alginate as immobilization matrices were examined and compared for the uptake of gold by a fungal biomass. PVA-immobilized biomass showed superior mechanical strength and chemical stability. In addition, PVA beads were also stable under a wider range of pH (1-13). The lower mass transfer resistance in PVA beads was evident from kinetic studies which showed a significantly shorter period of time for the immobilized PVA beads to achieve 80% gold removal as compared with immobilized alginate beads. Calculated rate constants and maximum rates for the uptake of gold by both immobilized PVA and immobilized alginate biosorbent revealed a much more rapid uptake phenomenon by the former. BET analyses also indicated a larger surface area and larger pore size distribution in PVA beads, further indicating a lower resistance to mass transfer. Gold biosorption in the immobilized PVA bead could be modeled by both the Langmuir and Freundlich adsorption isotherms.

Lysozyme-coupled poly(poly(ethylene glycol) methacrylate)-stainless steel hybrids and their antifouling and antibacterial surfaces.

An environmentally benign approach to impart stainless steel (SS) surfaces with antifouling and antibacterial functionalities was described. Surface-initiated atom transfer radical polymerization (ATRP) of poly(ethylene glycol) monomethacrylate) (PEGMA) from the SS surface-coupled catecholic L-3,4-dihydroxyphenylalanine (DOPA) with terminal alkyl halide initiator was first carried out, followed by the immobilization of lysozyme at the chain ends of poly(ethylene glycol) branches of the grafted PEGMA polymer brushes. The functionalized SS surfaces were shown to be effective in preventing bovine serum albumin (BSA) adsorption and in reducing bacterial adhesion and biofilm formation. The surfaces also exhibited good bactericidal effects against Escherichia coli and Staphylococcus aureus. The concomitant incorporation of antifouling hydrophilic brushes and antibacterial enzymes or peptides onto metal surfaces via catecholic anchors should be readily adaptable to other metal substrates, and is potentially useful for biomedical and biomaterial applications.

The influence of ionic strength, nutrients and pH on bacterial adhesion to metals.

Bacteria-metal interactions in aqueous solutions are important in biofilm formation, biofouling and biocorrosion problems in the natural environment and engineered systems. In this study, the adhesion forces of two anaerobes (Desulfovibrio desulfuricans and Desulfovibrio singaporenus) and an aerobe (Pseudomonas sp.) to stainless steel 316 in various aqueous systems were quantified using atomic force microscopy (AFM) with a cell probe. Results show that the nutrient and ionic strength of the solutions influence the bacteria-metal interactions. The bacteria-metal adhesion force was reduced in the presence of the nutrients in the solution, because a trace organic film was formed and thus decreased the metal surface wettability. Stronger ionic strength in the solution results in a larger bacteria-metal adhesion force, which is due to the stronger electrostatic attraction force between the positively charged metal surface and negatively charged bacterial surface. Solution pH also influences the interaction between the bacterial cells and the metal surface; the bacteria-metal adhesion force reached its highest value when the pH of the solution was near the isoelectric point of the bacteria, i.e. at the zero point charge. The adhesion forces at pH 9 were higher than at pH 7 due to the increase in the attraction between Fe ions and negative carboxylate groups.

Osmotic membrane bioreactor for wastewater treatment and the effect of salt accumulation on system performance and microbial community dynamics.

An osmotic membrane bioreactor was developed for wastewater treatment. The effects of salt accumulation on system performance and microbial community dynamics were investigated. Evident deterioration of biological activity, especially nitrification, was observed, which resulted in significant accumulation of organic matter and NH4(+)-N within the bioreactor. Arising from the elevation of salinity, almost all the dominant species was taken over by high salt-tolerant species. Significant succession among different species of Nitromonas was observed for ammonia-oxidizing bacteria. For nitrite-oxidizing bacteria, Nitrospira was not evidently affected, whereas Nitrobacter was eliminated from the system. Salt accumulation also caused significant shifts in denitrifying bacterial community from α- to γ-Proteobacteria members. Overall, the microbial community adapted to the elevated salinity conditions and brought about a rapid recovery of the biological activity. Membrane fouling occurred but was insignificant. Biofouling and inorganic scaling coexisted, with magnesium/calcium phosphate/carbonate compounds identified as the inorganic foulants.

Use of polyvinyl alcohol as a cell immobilization matrix for copper biosorption by yeast cells

Although polyvinyl alcohol (PVA) gel has been used as a carrier for immobilized cells and enzymes, its use as an immobilization matrix for inactivated cells for biosorption studies has not been reported. In this study, we have demonstrated that the PVA matrix showed very favourable performance, vis-a-vis good physical and chemical properties, and a low mass transfer resistance. The PVA matrix showed negligible effect on the uptake capacity of the inactivated yeast used as the biosorbent. Biosorption equilibrium showed that the specific copper uptake of the biomass increased with an increase in the initial copper concentration, and decreased with an increase in biomass loading. The equilibrium was well described by Langmuir and Freundlich adsorption isotherms. Temperature over the range of 10–50 °C had little effect on the biomass biosorption capacity, while pH showed significant effect. The PVA–yeast beads could be regenerated using 10 mmol dm−3 HCl, with up to 100% recovery, and the beads reused in five biosorption–desorption cycles with negligible decrease in the biosorption capacity. © 2000 Society of Chemical Industry

Characterization of corrosive bacterial consortia isolated from petroleum-product-transporting pipelines

Microbiologically influenced corrosion is a problem commonly encountered in facilities in the oil and gas industries. The present study describes bacterial enumeration and identification in diesel and naphtha pipelines located in the northwest and southwest region in India, using traditional cultivation technique and 16S rDNA gene sequencing. Phylogenetic analysis of 16S rRNA sequences of the isolates was carried out, and the samples obtained from the diesel and naphtha-transporting pipelines showed the occurrence of 11 bacterial species namely Serratia marcescens ACE2, Bacillus subtilis AR12, Bacillus cereus ACE4, Pseudomonas aeruginosa AI1, Klebsiella oxytoca ACP, Pseudomonas stutzeri AP2, Bacillus litoralis AN1, Bacillus sp., Bacillus pumilus AR2, Bacillus carboniphilus AR3, and Bacillus megaterium AR4. Sulfate-reducing bacteria were not detected in samples from both pipelines. The dominant bacterial species identified in the petroleum pipeline samples were B. cereus and S. marcescens in the diesel and naphtha pipelines, respectively. Therefore, several types of bacteria may be involved in biocorrosion arising from natural biofilms that develop in industrial facilities. In addition, localized (pitting) corrosion of the pipeline steel in the presence of the consortia was observed by scanning electron microscopy analysis. The potential role of each species in biofilm formation and steel corrosion is discussed.

Direct phosphorus recovery from municipal wastewater via osmotic membrane bioreactor (OMBR) for wastewater treatment.

This work reports, for the first time, a new approach to direct phosphorus recovery from municipal wastewater via an osmotic membrane bioreactor (OMBR). In the OMBR, organic matter and NH4(+) were removed by biological activities. PO4(3)(-), Ca(2+), Mg(2+) and unconverted NH4(+) were rejected by the forward osmosis (FO) membrane and enriched within the bioreactor. The resultant phosphorus-rich supernatant was then used for phosphorus recovery. By adjusting the pH to 8.0-9.5, PO4(3)(-) was recovered via precipitation with Ca(2+), Mg(2+) and NH4(+). The OMBR showed up to 98% overall removal of TOC and NH4(+)-N. At pH 9.0, more than 95% PO4(3)(-)-P was recovered without addition of magnesium and calcium. The precipitates were predominantly amorphous calcium phosphate (ACP) with phosphorus content >11.0%. In principal, this process can recover almost all the phosphorus, apart from the portion assimilated by bacteria. The global phosphorus recovery efficiency was shown to be 50% over 84 days.

Inorganic−Organic Hybrid Coatings on Stainless Steel by Layer-by-Layer Deposition and Surface-Initiated Atom-Transfer-Radical Polymerization for Combating Biocorrosion

To improve the biocorrosion resistance of stainless steel (SS) and to confer the bactericidal function on its surface for inhibiting bacterial adhesion and biofilm formation, well-defined inorganic-organic hybrid coatings, consisting of the inner compact titanium oxide multilayers and outer dense poly(vinyl-N-hexylpyridinium) brushes, were successfully developed. Nanostructured titanium oxide multilayer coatings were first built up on the SS substrates via the layer-by-layer sol-gel deposition process. The trichlorosilane coupling agent, containing the alkyl halide atom-transfer-radical polymerization (ATRP) initiator, was subsequently immobilized on the titanium oxide coatings for surface-initiated ATRP of 4-vinylpyridine (4VP). The pyridium nitrogen moieties of the covalently immobilized 4VP polymer, or P(4VP), brushes were quaternized with hexyl bromide to produce a high concentration of quaternary ammonium salt on the SS surfaces. The excellent antibacterial efficiency of the grafted polycations, poly(vinyl-N-pyridinium bromide), was revealed by viable cell counts and atomic force microscopy images of the surface. The effectiveness of the hybrid coatings in corrosion protection was verified by the Tafel plot and electrochemical impedance spectroscopy measurements.

Electroless recovery of precious metals from acid solutions by n-containing electroactive polymers

Summary form only given. By coupling the metal reduction process in acid solutions with an increase in the intrinsic oxidation state of a N-containing electroactive polymer, such as polypyrrole (PPY), polyaniline (PAN) and their derivatives, and the subsequent reprotonation and reduction of the intrinsically oxidized polymer in acid media, spontaneous and sustained reduction of precious metals, gold in particular, to their elemental form is achieved. The rate of metal reduction is dependent on the intrinsic redox states of the polymer, the effective surface area of the polymer, and the pH of the solution. The X-ray photoelectron spectroscopic (XPS) Nls core-level spectra of protonated and deprotonated PPY and PAN after metal reduction suggest that the intrinsic structure of each polymer at the polymer/Au interface remains intact, even at [Au]/[N] mole ratio much greater than 1. The process, however, is limited by the decreasing effective surface area of the polymer due to metal coverage. Nevertheless, a typical polymer film is capable of accumulating more than 5 times its own weight of Au before the reduction rate is severely retarded.