4 results on '"Xiaozhong Fang"'
Search Results
2. Surface-enhanced Raman Spectroscopy Facilitates the Detection of Microplastics < 1 μm in the Environment
- Author
-
Guanjun Xu, Ventsislav K. Valev, Xiaozhong Fang, Kedong Gong, Yiqing Feng, Hanyun Cheng, Robin Jones, Liwu Zhang, Kejian Li, and Muhammad Ali Tahir
- Subjects
Microplastics ,Materials science ,Nanotechnology ,Substrate (electronics) ,010501 environmental sciences ,Spectrum Analysis, Raman ,01 natural sciences ,symbols.namesake ,chemistry.chemical_compound ,SDG 3 - Good Health and Well-being ,Humans ,Environmental Chemistry ,Nanoscopic scale ,0105 earth and related environmental sciences ,General Chemistry ,Surface-enhanced Raman spectroscopy ,Orders of magnitude (numbers) ,Ray ,chemistry ,symbols ,Polystyrenes ,Gold ,Polystyrene ,Raman spectroscopy ,Plastics ,Water Pollutants, Chemical - Abstract
Micro- and nanoplastics are considered one of the top pollutants that threaten the environment, aquatic life and mammalian (including human) health. Unfortunately, the development of uncomplicated but reliable analytical methods that are sensitive to individual microplastic particles, with sizes smaller than 1 μm, remains incomplete. Here, we demonstrate the detection and identification of (single) micro- and nanoplastics, by using surface-enhanced Raman spectroscopy (SERS), with Klarite substrates. Klarite is an exceptional SERS substrate; it is shaped as a dense grid of inverted pyramidal cavities, made of gold. Numerical simulations demonstrate that these cavities (or pits) strongly focus incident light into intense hotspots. We show that Klarite has the potential to facilitate the detection and identification of synthesized and atmospheric/aquatic microplastic (single) particles, with sizes down to 360 nm. We find enhancement factors of up to two orders of magnitude for polystyrene analytes. In addition, we detect and identify microplastics with sizes down to 450 nm on Klarite, with samples extracted from ambient, airborne particles. Moreover, we demonstrate Raman mapping as a fast detection technique for sub-micron microplastic particles. The results show that SERS with Klarite is a facile technique that has the potential to detect and systematically measure nanoplastics in the environment. This research is an important step towards detecting nanoscale plastic particles that may cause toxic effects to mammalian and aquatic life when present in high concentrations.
- Published
- 2020
- Full Text
- View/download PDF
3. Boosting photocatalytic chlorophenols remediation with addition of sulfite and mechanism investigation by in-situ DRIFTs
- Author
-
Kejian Li, Liwu Zhang, Iqra Nabi, Xiaozhong Fang, Zhaoyang Fu, Yiqing Feng, Aziz-Ur-Rahim Bacha, and Yang Yang
- Subjects
021110 strategic, defence & security studies ,Muconic acid ,Environmental Engineering ,Quenching (fluorescence) ,Hydroquinone ,Health, Toxicology and Mutagenesis ,0211 other engineering and technologies ,02 engineering and technology ,010501 environmental sciences ,Photochemistry ,01 natural sciences ,Pollution ,Bisulfite ,chemistry.chemical_compound ,chemistry ,Sulfite ,Photocatalysis ,Environmental Chemistry ,Phenol ,Photodegradation ,Waste Management and Disposal ,0105 earth and related environmental sciences - Abstract
Sulfite is recently found to be promising in enhancing photocatalytic pollutants degradation, and it is a byproduct from flue gas desulfuration process. Herein, 4-chlorophenol (4-CP) photodegradation was systematically investigated in a sulfite mediated system with g-C3N4 as photocatalyst. The degradation efficacy was improved by about 3 times with addition of 25 mM Na2SO3. The dominant responsible reactive oxygen species for chlorophenols remediation in the presence of sulfite included O2·-, SO3·-, and SO4·- as confirmed by radical quenching experiments and electron spin resonances technology. In-situ DRIFTs results indicated the improved cleavage of C-Cl and C-H bonds with the simultaneous formation of C O and C C bonds when bisulfite was added. Degradation intermediates such as 4-chlorocatechol, hydroquinone, and muconic acid were detected by HPLC-MS. Furthermore, the photodegradation mechanisms were discussed in the presence of sulfite. Other chlorophenols (phenol, 2-CP, 2,4-DCP, and their mixture) were also efficiently removed in the system, suggesting that sulfite could be universally applied in photocatalytic wastewater purification.
- Published
- 2020
4. Brown carbon: An underlying driving force for rapid atmospheric sulfate formation and haze event
- Author
-
Tao Wang, Yangyang Liu, Yue Deng, Xiaozhong Fang, Liwu Zhang, Iqra Nabi, Hanyun Cheng, and Aziz Ur Rahim Bacha
- Subjects
chemistry.chemical_classification ,Environmental Engineering ,Haze ,010504 meteorology & atmospheric sciences ,Chemistry ,010501 environmental sciences ,Particulates ,complex mixtures ,01 natural sciences ,Pollution ,Aerosol ,Atmosphere ,chemistry.chemical_compound ,Environmental chemistry ,Atmospheric chemistry ,Environmental Chemistry ,Humic acid ,Hydroxyl radical ,Sulfate ,Waste Management and Disposal ,0105 earth and related environmental sciences - Abstract
The rapid sulfate formation is a crucial factor determining the explosive growth of fine particles and the frequent occurrence of severe haze events in China. Recent field observations also show that brown carbon is one of the most critical components in aerosol particles sampled during haze episodes. To this day, there is limited knowledge that accesses the role of brown carbon in atmospheric chemistry. In fact, these carbonaceous particulate matters, mainly derived from forest fires, biomass burning, and biogenic release, can act as photosensitizers and produce varieties of active intermediates to alter oxidation capacity. Experimental results in this work provide evidence that hydroxyl radical (∙OH) stems from brown carbon proxies fulvic acid /humic acid (FA/HA) upon irradiation, leading to rapid SO2 oxidation on brown carbon particles in the atmosphere. Further correlation analyses for sulfate formation and chromophore properties of 12 model compounds demonstrate that brown carbon particles with higher aromaticity and E2/E3 (the ratio of absorbance at 254 nm to that at 365 nm) would facilitate ∙OH production and SO2 photo-oxidation. Uptake coefficient measurements and sulfate production rate estimation indicate that brown carbon could gain importance in atmospheric SO2 oxidation. A better understanding of SO2 uptake kinetics on brown carbon surfaces favors in defining new regulations to improve air quality and reduce the harmful effects of haze events on resident health and the environment.
- Published
- 2020
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.