Yu-Tzu Huang

Simultaneous partial nitrification, anaerobic ammonium oxidation and denitrification (SNAD) in a full-scale landfill-leachate treatment plant

The occurrence of simultaneous partial nitrification, anaerobic ammonium oxidation and denitrification (SNAD) observed in a single partially aerated full-scale bioreactor treating landfill-leachate is reported in this paper. At present, the full-scale bioreactor is treating an average leachate flow of 304 m(3)d(-1) with a sludge retention time between 12 and 18d. The average COD, NH(4)(+)-N and NO(3)(-)-N concentrations at the upstream end of the bioreactor, i.e., influent, are 554, 634 and 3 mg L(-1), respectively; whereas no NO(2)(-)-N is detected in the influent. The percentage removals of COD and NH(4)(+)-N in the bioreactor were 28% and 80%, respectively. A nitrogen mass balance approach was adopted to analyze the performance of SNAD in the full-scale bioreactor. The total nitrogen (TN) removal by combined partial nitrification and anaerobic ammonium oxidation is 68% and the heterotrophic denitrification contributes to 8% and 23% of TN and COD removals, respectively. The red granule in the bioreactor was analyzed by using fluorescence in situ hybridization and polymerase chain reaction. The results of both analytical methods confirm the presence of anaerobic ammonium oxidizing bacteria as the predominant species along with other Planctomycete-like bacteria. Overall, the SNAD process offers the simultaneous removals of nitrogen and COD in the wastewater.

Partial nitrification and anammox process: A method for high strength optoelectronic industrial wastewater treatment

Completely autotrophic nitrogen removal over nitrite (CANON) process was employed in an 18 L sequencing batch reactor (SBR) for treatment of optoelectronic industrial wastewater containing high strength ammonium nitrogen (3712 ± 120 mg NH4(+) - N L(-1)). About 89% of total nitrogen and 98% of NH4(+) - N removal efficiencies were observed at the loading rate of 909 g N m(-3) d(-1) and the HRT of 4 d. A profound variation in the performance of CANON process was experienced at high DO exposure (above 1 mg L(-1)) and high nitrite concentration (above 100 mg L(-1)). Inhibition due to high DO exposure was found to be reversible phenomenon whereas the synergistic inhibition of nitrite, free ammonia and free nitrous acid was irreversible. The fluctuation of reactor temperature between 17 and 37 °C did not affect the performance of CANON system. The CANON process was stably controlled at high nitrogen loading rate for more than one month. The co-existence of aerobic and anaerobic ammonium oxidizing bacteria in the reactor was detected by The PCR analysis. About 5 fold increase in amount of anammox bacteria over a period of 258 days was confirmed from the results of qPCR on day 487.

Functionalized Fe3O4@Silica Core–Shell Nanoparticles as Microalgae Harvester and Catalyst for Biodiesel Production

Core-shell Fe3O4@silica magnetic nanoparticles functionalized with a strong base, triazabicyclodecene (TBD), were successfully synthesized for harvesting microalgae and for one-pot microalgae-to-fatty acid methyl ester (FAME, or so-called biodiesel) conversion. Three types of algae oil sources (i.e., dried algae, algae oil, and algae concentrate) were used and the reaction conditions were optimized to achieve the maximum biodiesel yield. The results obtained in this study show that our TBD-functionalized Fe3O4@silica nanoparticles could effectively convert algae oil to biodiesel with a maximum yield of 97.1 %. Additionally, TBD-Fe3O4@silica nanoparticles act as an efficient algae harvester because of their adsorption and magnetic properties. The method presented in this study demonstrates the wide scope for the use of covalently functionalized core-shell nanoparticles for the production of liquid transportation fuels from algal biomass.

Start-up of simultaneous partial nitrification, anammox and denitrification (SNAD) process in sequencing batch biofilm reactor using novel biomass carriers.

Simultaneous partial nitrification, anammox and denitrification (SNAD) process was started-up in a 2.5L sequencing batch biofilm reactor (SBBR) using novel biomass carriers. The SNAD process took only 51d for start-up at nitrogen loading rate (NLR) and organic loading rate (OLR) of 120 and 60g/m(3)-d, respectively. Long-term stable operation of SNAD process was observed at NLR and OLR of 360 and 180g/m(3)-d with average total nitrogen and COD removal efficiencies of >88% and >90%, respectively. The values of conversion ratio [Formula: see text] remained below 0.11 after the start-up period, which further confirmed the long-term stability of SNAD process. Results of polymerase chain reaction (PCR), qualitative PCR, and scanning electron microscopic (SEM) analysis of sludge samples confirmed the co-existence and enrichment of AOB, anammox bacteria and denitrifying bacteria in the reactor and biofilm formation on to the carriers.

Block-copolymer-assisted synthesis of hydroxyapatite nanoparticles with high surface area and uniform size

Abstract We report the synthesis of hydroxyapatite nanoparticles (HANPs) by the coprecipitation method using calcium D-gluconate and potassium hydrogen phosphate as the sources of calcium and phosphate ions, respectively, and the triblock copolymer F127 as a stabilizer. The HANPs were characterized using scanning electron microscopy, x-ray diffraction, and nitrogen adsorption/desorption isotherms. Removal of F127 by solvent extraction or calcination alters the structure of HANPs. The solvent-extracted HANPs were single crystals with their 〈001〉 axis oriented along the rod axis of the HANP, whereas the calcined HANPs contained two crystal phases that resulted in a spherical morphology. The calcined HANPs had much higher surface area (127 m2 g−1) than the solvent-extracted HANPs (44 m2 g−1).

Preparation of Ordered Mesoporous Alumina‐Doped Titania Films with High Thermal Stability and Their Application to High‐Speed Passive‐Matrix Electrochromic Displays

Ordered mesoporous alumina-doped titania thin films with anatase crystalline structure were prepared by using triblock copolymer Pluronic P123 as structure-directing agent. Uniform Al doping was realized by using aluminum isopropoxide as a dopant source which can be hydrolyzed together with titanium tetraisopropoxide. Aluminum doping into the titania framework can prevent rapid crystallization to the anatase phase, thereby drastically increasing thermal stability. With increasing Al content, the crystallization temperatures tend to increase gradually. Even when the Al content doped into the framework was increased to 15 mol %, a well-ordered mesoporous structure was obtained, and the mesostructural ordering was still maintained after calcination at 550 °C. During the calcination process, large uniaxial shrinkage occurred along the direction perpendicular to the substrate with retention of the horizontal mesoscale periodicity, whereby vertically oriented nanopillars were formed in the film. The resulting vertical porosity was successfully exploited to fabricate a high-speed and high-quality passive-matrix electrochromic display by using a leuco dye. The vertical nanospace in the films can effectively prevent drifting of the leuco dye.

Evaluating the antibacterial property of gold-coated hydroxyapatite: a molecular biological approach.

Hydroxyapatite nanoparticles (HAP NPs) are one of the widely used biocompatible materials. However, information about the reaction between HAP NPs and microorganisms is insufficient. This paper aims to understand the antibacterial property of a new nanocomposite consisting of gold-coated HAP and alginate polymer (namely, Au-HAP@Alg NPs). To the best of our knowledge, we reported the first information regarding to MIC (25mg/mL), DIZ (no visible zone), and IC50 (0.5mg/mL) of Au-HAP@Alg NPs toward the microorganism Escherichia coli TOP10. The real-time gene expression levels of polA, polB, cyd, mdoG, GAPDH, and 16S rRNA were maintained at stable levels up until conditions of 2.5mg/mL Au-HAP@Alg NPs. The results showed that 16S rRNA can be a good reference under these conditions. The expressions of GAPDH, cyd, and mdoG were inhibited obviously under condition of 10mg/mL of Au-HAP@Alg NPs. Our results indicated that the possible antibacterial mechanism of Au-HAP@Alg was through the interaction with these carbohydrate and cell wall-related genes. This novel biocompatible and antibacterial material can potentially be applied in medical and environmental fields.