Publications by authors named "Fumin Peng"

The integration of photocatalysis and biological treatment provides an effective strategy for controlling antibiotic contamination, which requires precise monitoring of toxicity changes during the photocatalytic process. In this study, nanoscale TiO (P25) was employed to degrade tetracycline (TC) under full-spectrum irradiation, with O identified as a crucial reactant for the generation reactive oxygen species (ROS). The toxicity simulation results of the degradation intermediates were closely correlated with the predictions of T.

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Electroencephalogram (EEG) was used to analyze the mechanisms and differences in brain neural activity of drivers in visual, auditory, and cognitive distracted vs. normal driving emergency braking conditions. A pedestrian intrusion emergency braking stimulus module and three distraction subtasks were designed in a simulated experiment, and 30 subjects participated in the study.

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A novel Ce(iii) ion-implanted aluminum-trimesic metal-organic framework (Ce-MIL-96) was synthesized for the first time via alcohol-solvent incipient wetness impregnation. Compared to previously reported Ce-contained adsorbents, the fluoride adsorption performance of the new ion-implanted metal-organic framework demonstrated much higher adsorption capacity and more efficient regeneration of Ce. In a wide pH range of 3 to 10, Ce-MIL-96 maintained constant adsorption performance for fluoride, and the residual Ce and Al in the treated solution were below the safe limits in drinking water.

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We show a step-by-step strategy to fabricate MOF related core-shell heterostructures and successfully obtain SiO2@HKUST-1 core-shell nanospheres, which display the distinct ion separation ability of valving the sorption-desorption of fluoride ions by controlling the pH.

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Metal-organic frameworks (MOFs) MIL-88A hexagonal microrods as a new photocatalyst show an active performance for methylene blue (MB) dye decolorization using visible light. MB decolorization over the MIL-88A photocatalyst follows first-order kinetics. The addition of a H2O2 electron acceptor can markedly enhance the photocatalytic MB decoloration performance of MIL-88A.

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The presence of coordinatively unsaturated metal centers in metal-organic frameworks (MOFs) provides an accessible way to selectively functionalize MOFs through coordination bonds. In this work, we describe thiol-functionalization of MOFs by choosing a well known three-dimensional (3D) Cu-based MOF, i.e.

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The photocatalytic decolorization of methylene blue dye in aqueous solution using a novel photocatalyst MIL-53(Fe) metal-organic frameworks was investigated under UV-vis light and visible light irradiation. The effect of electron acceptor H(2)O(2), KBrO(3) and (NH(4))(2)S(2)O(8) addition on the photocatalytic performance of MIL-53(Fe) was also evaluated. The results show that MIL-53(Fe) photocatalyst exhibited photocatalytic activity for MB decolorization both under UV-vis light and visible light irradiation, and the MB decolorization over MIL-53(Fe) photocatalyst followed the first-order kinetics.

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A novel type of magnetic porous carbonaceous polymeric material, CTF/Fe(2)O(3) composite (CTF = covalent triazine-based framework), has been synthesized by a facile microwave-enhanced high-temperature ionothermal method. By selecting ZnCl(2) as a reaction medium and the Lewis acid catalyst, and choosing FeCl(3)·6H(2)O as an iron oxide precursor, a series of CTF/Fe(2)O(3) composites with different γ-Fe(2)O(3) contents has been prepared in 60 min. The resulting samples were characterized by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and N(2) sorption-desorption isotherms.

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Ozone (O3) often serves as the benchmark for the overall pollution level of a given airshed and it is critical that the measurement technique be accurate and precise, In the DOAS measurement, the accuracy of O3 concentration is determined by the selected spectral range. The present paper focuses on the effect of spectral range on the detected characteristic absorption structure of O3, and the variation of differential cross section of O3 with the change in spectral range and the source of interference in different spectral range. The effect of practical atmospheric light extinction on the light intensities of different spectral ranges was deduced; the effect of spectral range on the accuracy was determined by detecting the standard gases at different concentration and different spectral resolution.

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Based on the differential optical absorption spectroscopy (DOAS) technology, the measurement of air pollutants (SOz, NO2, HONO and HCHO) was performed continuously from Jan 19, 2007 to Feb 8, 2007 in Peking University campus. The typical diurnal variation characteristic of SO2 concentration, the main source and the meteorological factors that influence the pollutants were analyzed. The results indicated that the typical diurnal variation of SO2 concentration has the same shape as the letter "V" when wind speed was low, and in the afternoon the SO2 concentration was the lowest, while in other time it was high.

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The method of retrieving the concentration of trace gases using of the diagnostic absorption of trace gases based on the scattered sunlight is called passive DOAS. It has been developed so fast in recent years because it remains simple and is prone to being combined with different platform. While retrieving the column density of trace gases with the scattered sunlight as light source, it will be affected strongly by solar Fraunhofer lines, which is also called Ring effect.

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Featuring excellent response characteristics and detection sensitivity and with much lower operational cost, differential optical absorption spectroscopy (DOAS) can be a powerful tool to trace the concentration variation of carbon bisulfide (CS2), a kind of poisonous gas with bad smell. In the DOAS measurement, the accuracy of the carbon bisulfide results is determined by the selected spectral resolution. The present paper focuses on the effect of resolution on the detected characteristic absorption structure of CS2 and the variation in differential cross section of CS2 with the change in resolution, from which the effect of resolution on the detection limit of CS2 is deduced.

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The excellent response characteristics and detection sensitivity with much lower operational cost and the capability to discriminate between the isomer of some monoaromatic hydrocarbons (MAHCs) make differential optical absorption spectroscopy (DOAS) a powerful tool to trace concentration variation of MAHCs. But due to the similarity in chemical structure, those MAHCs have the similar overlapped characteristic absorption structures, which make the selection of instrumental parameter critical to the accurate detection of MAHCs. Firstly, the spectral resolution used in DOAS system determines the nonlinear absorption of O2 and the mass dependence of characteristic absorption structure; thereby it determines the effect of elimination error of O2 absorption in the atmospheric spectra for the detection of MAHCs.

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Observation of nighttime nitrate radical (NO3) was performed by using long path differential optical absorption spectroscopy (LP-DOAS), on the outskirts of Hefei, China. The time series of NO3 and supporting parameters were simultaneously measured for a week (31 May-7 June 2006). The results indicated that the average concentration of NO3 was 15.

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Featuring excellent response characteristics and detection sensitivity and with much lower operational cost, differential optical absorption spectroscopy (DOAS) can be a powerful tool to trace concentration variation of trace indicators -O3, Ox (O3 + NO2) and HCHO for fast VOCs atmospheric photochemistry. But it's difficult to measure those gases accurately because of trace concentration. Here using a self-made DOAS system, the accurate measurement of those indicators was achieved through improving the ratio of signal to noise ratio and correcting the background scattering light; the retrieving method of those indicators was developed through eliminating the temperature effect of absorption cross section, accurately removing the intrinsic structure and lamp structure of spectrum.

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Steam distillation (SD), simultaneous distillation and extraction (SDE) and headspace co-distillation (HCD) were compared here for their effectiveness in the extraction of volatile compounds from tobacco. The different grades of aged flue-cured tobacco leaves extracted by the three methods respectively were analyzed using GC-MS. Mass spectra or authentic compounds were used to identify around 408 components in various volatile fractions.

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