23 research outputs found
A paper/polymer hybrid CD-like microfluidic SpinChip integrated with DNA-functionalized graphene oxide nanosensors for multiplex qLAMP detection
© 2017 The Royal Society of Chemistry. A paper/poly(methyl methacrylate) (PMMA) hybrid CD-like microfluidic SpinChip integrated with DNA probe-functionalized graphene oxide (GO) nanosensors was developed for multiplex quantitative LAMP detection (mqLAMP). This approach can simply and effectively address a major challenging problem of multiplexing in current LAMP methods
Highly Efficient Antibacterial and Pb(II) Removal Effects of Ag-CoFe<sub>2</sub>O<sub>4</sub>‑GO Nanocomposite
Ag-CoFe<sub>2</sub>O<sub>4</sub>-graphene oxide (Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO) nanocomposite was synthesized by doping silver and CoFe<sub>2</sub>O<sub>4</sub> nanoparticles on the surface of GO, which was
used to purify both bacteria and PbÂ(II) contaminated water. The Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO nanomaterial was characterized by transmission
electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform
infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopy
(XPS), Brunauer-Emmett-Teller (BET), cyclic voltammetry (CV), and
magnetic property tests. It can be found that Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO nanocomposite exhibited excellent antibacterial activity
against Gram-negative <i>Escherichia coli</i> and Gram-positive <i>Staphylococcus aureus</i> compared with CoFe<sub>2</sub>O<sub>4</sub>, Ag-CoFe<sub>2</sub>O<sub>4</sub>, and CoFe<sub>2</sub>O<sub>4</sub>-GO composite. This superior disinfecting effect was possibly
attributed to the combination of GO nanosheets and Ag nanoparticles.
Several antibacterial factors including temperature, time, and pH
were also investigated. It was obvious that <i>E. coli</i> was more susceptible than <i>S. aureus</i> toward all
the four types of nanomaterials. The structural difference of bacterial
membranes should be responsible for the resistant discrepancy. We
also found that Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO inactivated both
bacteria in an irreversibly stronger manner than Ag-CoFe<sub>2</sub>O<sub>4</sub> and CoFe<sub>2</sub>O<sub>4</sub>-GO. The PbÂ(II) removal
efficiency with all the nanomaterials showed significant dependence
on the surface area and zeta potential of the materials. In this work,
not only did we demonstrate the simultaneous superior removal efficiency
of bacteria and PbÂ(II) by Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO but
also the antibacterial mechanism was discussed to have a better understanding
of the interaction between Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO and
bacteria. In a word, taking into consideration the easy magnetic separation,
bulk availability, and irreversibly high antibacterial activity of
Ag-CoFe<sub>2</sub>O<sub>4</sub>-GO, it is the very promising candidate
material for advanced antimicrobial or PbÂ(II) contaminated water treatment
The inter-connected porous CuOx-NbOx/kit-CeO2 catalyst:Enhanced activity, resistance of SO2 and H2O for the removal of NOx
In order to remove NOx from multiple sources with complex operating conditions, catalysts with excellent low-temperature activity and strong water and sulfur resistance are in high demand. Herein, we designed an efficient inter-connected porous CuOx-NbOx/kit-CeO2 catalyst for the selective catalytic reduction of NOx with NH3 (NH3-SCR). The catalyst exhibited relatively outstanding NH3-SCR activity in the low temperature range (100–300 °C) and showed remarkable stability and excellent resistance to SO2 and H2O. The inter-connected porous structure allowed the adsorption and diffusion of gaseous reactants, meanwhile, the interaction between Cu, Nb and Ce enhanced the surface acidity, redox properties and surface oxygen activity of the CuOx-NbOx/kit-CeO2 catalyst. On the basis of in situ DRIFTs studies, Eley-Rideal process was expected to be the dominant pathway with the coexistence of Langmuir–Hinshelwood mechanism at 250 °C
Novel Flexible Self-Standing Pt/Al<sub>2</sub>O<sub>3</sub> Nanofibrous Membranes: Synthesis and Multifunctionality for Environmental Remediation
In
spite of intensive research investigating the prevalent Pt/Al<sub>2</sub>O<sub>3</sub> catalysts, achieving macroscopic morphology
beyond the powder form limitations remains highly challenging. Meanwhile,
current impregnation-based preparation approaches show the drawbacks
of tedious procedures and inefficient use of noble metals. Therefore,
it is important to search for new methods for the fabrication of Pt/Al<sub>2</sub>O<sub>3</sub> catalysts with a novel morphology. In this study,
a novel Pt/Al<sub>2</sub>O<sub>3</sub> nanofibrous membrane catalyst
is fabricated via a facile one-pot electrospinning process. The embedding
of Pt nanoparticles is performed simultaneously with the formation
of Al<sub>2</sub>O<sub>3</sub> nanofibers. The Pt/Al<sub>2</sub>O<sub>3</sub> membranes show remarkable mechanical properties with tensile
stresses as high as 44.14 MPa. Notably, the Pt/Al<sub>2</sub>O<sub>3</sub> membranes exhibit multifunctionality with excellent performance
characteristics. The catalytic experiments indicate that 100% of bisphenol
A is removed within 60 min, and 100% of CO is completely converted
to CO<sub>2</sub> at 242 °C when Pt/Al<sub>2</sub>O<sub>3</sub> membranes are used as catalysts. The membranes also exhibit excellent
filtration performance, clearly decreasing the turbidity of water,
and meet the high efficiency of particulate air filter standards.
The excellent flexibility, satisfying mechanical property, and multifunctionality
extend the range of potential application of the Pt/Al<sub>2</sub>O<sub>3</sub> membranes. Moreover, the facile synthesis suggests
new possibilities for the fabrication of many membrane-form Al<sub>2</sub>O<sub>3</sub>-supported catalysts
Fabrication of TiO<sub>2</sub>–Bi<sub>2</sub>WO<sub>6</sub> Binanosheet for Enhanced Solar Photocatalytic Disinfection of <i>E. coli</i>: Insights on the Mechanism
TiO<sub>2</sub>–Bi<sub>2</sub>WO<sub>6</sub> binanosheet (TBWO), synthesized by a facile two-step
hydrothermal method, was used as an effective visible-light-driven
photocatalyst for the inactivation of <i>E. coli</i> and
was characterized by TEM, SEM, XRD, FTIR, XPS, and BET. A series of
TBWOs with different doping ratios of TiO<sub>2</sub> loading from
10 to 55 wt % were synthesized. Among all of the TBWOs, 40% TBWO exhibited
the best bacteria disinfection efficiency, and the quantity of viable
bacteria could reach 10° with 40% TBWO (100 μg/mL) after
being illuminated for 4 h. Furthermore, the confocal fluorescent-based
cell live/dead test and the SEM technology were applied to verify
the photocatalytically lethal effect toward <i>E. coli</i> and the rupture of bacterial membranes. The leak of bacterial contents,
including the bacterial genome represented by relevant 16srDNA, and
total protein were detected by PCR and bicinchoninic acid assay. In
this work, the antibacterial mechanism was studied by employing photoelectrochemical
techniques, electron spin resonance (ESR), and scavengers of different
reactive species, revealing the pivotal roles of electron hole (h<sup>+</sup>) and electron (e<sup>–</sup>) in the photocatalytic
process. In addition, the •O<sub>2</sub><sup>–</sup> and •OH radicals were also detected in the TBWOs system by
ESR. It was found that the adsorption of visible light and separation
of photogenerated carriers within TiO<sub>2</sub> have been largely
promoted after being coupled with Bi<sub>2</sub>WO<sub>6</sub>, which
should be responsible for the improved bactericidal effect
Energy-saving removal of methyl orange in high salinity wastewater by electrochemical oxidation via a novel Ti/SnO2-Sb anode-Air diffusion cathode system
Electrochemical oxidation is an effective method in removal of organic pollutant from high salinity waste-water (NaCl), by producing active chlorine at anode or hydrogen peroxide at cathode. To solve the existing problems including low efficiency, high cost and energy consumption, a Ti/SnO2-Sb anode (TSSA)-air diffusion cathode (TSSA-ADC) system was investigated for methyl orange (MO) removal from NaCl solution, using single TSSA system as control. The phase composition of TSSA was examined by X-ray diffraction. Accumulated concentrations of active chlorine, hydrogen peroxide, MO removal rate, TOC, pH value were recorded at different current densities. The results indicated that Sb-doped rutile SnO2 was formed on the TSSA. The TSSA and the ADC exhibited good catalysis to chlorine evolution and oxygen reduction, respectively. Although MO were almost completely removed in both systems, higher TOC removal, shorter running time and lower energy consumption were attained in the TSSA-ADC system. pH value was more stable (6.0-6.4) in the TSSA-ADC system than that in the TSSA system (6.0-9.4), predicting its stronger capacity in anti-scaling when treating high salinity wastewater with hard ions like Ca2+ and Mg2+. (C) 2015 Elsevier B.V. All rights reserved