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Chin-Pao Huang

Bio: Chin-Pao Huang is an academic researcher from University of Delaware. The author has contributed to research in topics: Adsorption & Chemistry. The author has an hindex of 69, co-authored 307 publications receiving 17355 citations. Previous affiliations of Chin-Pao Huang include Harvard University & Pennsylvania State University.


Papers
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TL;DR: In this article, the electro-optical and photocatalytic properties of the synthesized TiO2 nanoparticles were studied along with several commercially available ultra-fine TiO 2 particles (e.g., 3.8-5.7nm).
Abstract: Anatase TiO2 nanocrystallines (17–29 nm) were successfully synthesized by the metal–organic chemical vapor deposition method (MOCVD). Moderate manipulation of system parameters of MOCVD can control the particle size. The electro-optical and photocatalytic properties of the synthesized TiO2 nanoparticles were studied along with several commercially available ultra-fine TiO2 particles (e.g., 3.8–5.7 nm). The band gap of the TiO2 crystallines was determined using the transformed diffuse reflectance technique according to the Kubelka–Munk theory. Results showed that the band gap of TiO2 monotonically decreased from 3.239 to 3.173 eV when the particle size decreased from 29 to 17 nm and then increased from 3.173 to 3.289 eV as the particle size decreased from 17 to 3.8 nm. The results of band gap change as a function of particle size agreed well with what was predicted by the Brus’ equation, i.e., the effective mass model (EMM). However, results of the photocatalytic oxidation of 2-chlorophenol (2-CP), showed that the smaller the particle size, the faster the degradation rate. This is attributed in part to the combined effect of band gap change relative to the spectrum of the light source and the specific surface area (or particle size) of the photocatalysts. The change of band gap due to particle size represents only a small optical absorption window with respect to the total spectrum of the light source, i.e., from 380 to 400 nm versus >280 nm. Consequently, the gain in optical property of the larger particles was severely compromised by their decrease in specific surface area. Our results clearly indicated the importance of specific surface area in controlling the photocatalytic reactivity of photocatalysts. Results also showed that the secondary particle size grew with time due mainly to particle aggregation. The photocatalytic rate constants decreased exponentially with increase in primary particle size. Primary particle size alone is able to predict the photocatalytic rate as it is closely related to the electro-optical properties of photocatalysts.

768 citations

Journal ArticleDOI
TL;DR: The potential of advanced chemical oxidation for future hazardous wastes treatment is demonstrated by four AOP systems, namely, H2O2/Fe2+, TiO 2/uv/O2, H 2O22, and TiO2-uv/H2O 2, exemplified by chlorophenols.

519 citations

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TL;DR: In this article, the amphoteric properties of hydrous γ-Al2O3 and the distribution of earth alkaline cations in the oxide-electrolyte interface were evaluated from alkalimetric and acidimetric titration curves of aqueous dispersions.

494 citations

Journal ArticleDOI
TL;DR: In this article, the effects of pH and the iron-to-nitrate ratio on both nitrate reduction rate and percent removal were investigated, and the apparent reaction order with respect to nitrate was determined and a mass balance was obtained.

479 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, a literature review of the use of sorbents and biosorbents to treat polluted aqueous effluents containing dyes:organics or metal ions has been conducted.

13,746 citations

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TL;DR: The use of a solid hole conductor dramatically improved the device stability compared to (CH3NH3)PbI3 -sensitized liquid junction cells.
Abstract: We report on solid-state mesoscopic heterojunction solar cells employing nanoparticles (NPs) of methyl ammonium lead iodide (CH3NH3)PbI3 as light harvesters. The perovskite NPs were produced by reaction of methylammonium iodide with PbI2 and deposited onto a submicron-thick mesoscopic TiO2 film, whose pores were infiltrated with the hole-conductor spiro-MeOTAD. Illumination with standard AM-1.5 sunlight generated large photocurrents (JSC) exceeding 17 mA/cm2, an open circuit photovoltage (VOC) of 0.888 V and a fill factor (FF) of 0.62 yielding a power conversion efficiency (PCE) of 9.7%, the highest reported to date for such cells. Femto second laser studies combined with photo-induced absorption measurements showed charge separation to proceed via hole injection from the excited (CH3NH3)PbI3 NPs into the spiro-MeOTAD followed by electron transfer to the mesoscopic TiO2 film. The use of a solid hole conductor dramatically improved the device stability compared to (CH3NH3)PbI3 -sensitized liquid junction cells.

6,751 citations

Journal ArticleDOI
TL;DR: In this article, the photocatalytic degradation of azo dyes containing different functionalities has been reviewed using TiO2 as photocatalyst in aqueous solution under solar and UV irradiation.
Abstract: The photocatalytic degradation of azo dyes containing different functionalities has been reviewed using TiO2 as photocatalyst in aqueous solution under solar and UV irradiation. The mechanism of the photodegradation depends on the radiation used. Charge injection mechanism takes place under visible radiation whereas charge separation occurred under UV light radiation. The process is monitored by following either the decolorization rate and the formation of its end-products. Kinetic analyses indicate that the photodegradation rates of azo dyes can usually be approximated as pseudo-first-order kinetics for both degradation mechanisms, according to the Langmuir–Hinshelwood model. The degradation of dyes depend on several parameters such as pH, catalyst concentration, substrate concentration and the presence of electron acceptors such as hydrogen peroxide and ammonium persulphate besides molecular oxygen. The presence of other substances such as inorganic ions, humic acids and solvents commonly found in textile effluents is also discussed. The photocatalyzed degradation of pesticides does not occur instantaneously to form carbon dioxide, but through the formation of long-lived intermediate species. Thus, the study focuses also on the determination of the nature of the principal organic intermediates and the evolution of the mineralization as well as on the degradation pathways followed during the process. Major identified intermediates are hydroxylated derivatives, aromatic amines, naphthoquinone, phenolic compounds and several organic acids. By-products evaluation and toxicity measurements are the key-actions in order to assess the overall process.

3,692 citations

Journal ArticleDOI
TL;DR: In this paper, the complex mechanisms of Fenton and Fenton-like reactions and the important factors influencing these reactions, from both a fundamental and practical perspective, in applications to water and soil treatment, are discussed.
Abstract: Fenton chemistry encompasses reactions of hydrogen peroxide in the presence of iron to generate highly reactive species such as the hydroxyl radical and possibly others. In this review, the complex mechanisms of Fenton and Fenton-like reactions and the important factors influencing these reactions, from both a fundamental and practical perspective, in applications to water and soil treatment, are discussed. The review covers modified versions including the photoassisted Fenton reaction, use of chelated iron, electro-Fenton reactions, and Fenton reactions using heterogeneous catalysts. Sections are devoted to nonclassical pathways, by-products, kinetics and process modeling, experimental design methodology, soil and aquifer treatment, use of Fenton in combination with other advanced oxidation processes or biodegradation, economic comparison with other advanced oxidation processes, and case studies.

3,218 citations