120-83-2Relevant articles and documents
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Tarugi
, p. 491 (1900)
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Rh-catalyzed direct synthesis of 2,2′-dihydroxybenzophenones and xanthones
Rao, Maddali L. N.,Ramakrishna, Boddu S.
, p. 75505 - 75511 (2016)
An efficient rhodium-catalyzed direct synthesis of 2,2′-dihydroxybenzophenones and xanthones was developed from functionalized salicylaldehydes. This approach provides an easy access to various functionalized 2,2′-dihydroxybenzophenone and xanthone core s
Kinetics of heterogeneous photocatalytic decomposition of 2,4-dichlorophenoxyacetic acid over titanium dioxide and zinc oxide in aqueous solution
Djebbar,Sehili
, p. 269 - 276 (1998)
The photocatalytic transformation of 2,4-D in aqueous solution containing a suspension of titanium dioxide or zinc oxide leads to the formation of intermediates which are totally mineralised to carbon dioxide and hydrogen chloride (2,4-dichlorophenol and chlorohydroquinone are the major intermediates). The products at the initial stage of the reaction were 2,4-dichlorophenol (2,4-DCP), chlorohydroquinone, 4-chloropyrocatechol, 2,4-dichloro-pyrocatechol and 1.4-chlorobenzoquinone. The initial rate of photodegradation was studied as a function of the initial concentration of reactants by the linearised form of the Langmuir-Hinshelwood equation, by which rate constants κ and equilibrium adsorption constants K were evaluated. These constants were calculated at different temperatures between 25 and 60°C. The photodegradation rate increased with increase of pH. The photocatalytic transformation of 2,4-D over titanium dioxide or zinc oxide in solution containing hydrogen peroxide was studied. The latter accelerated the reaction rate of 2,4-D significantly. It was found that chloride or bicarbonate ions slowed down the photo-degradation rate of 2,4-D by scavenging hydroxyl radicals. Partial inhibition by ethanol is attributed to scavenging of the OH radicals involved in the first step of the reaction.
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Laurent
, (1841)
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Sensitized photooxidation of triclosan pesticide. A kinetic study in presence of vitamin B2
Reynoso, Agustina,Possetto, David,De Gerónimo, Eduardo,Aparicio, Virginia C.,Natera, José,Massad, Walter
, (2021)
Kinetic and mechanistic aspects of Riboflavin (Rf, vitamin B2)-sensitized photochemical degradation of Triclosan (TCS) have been studied by time-resolved and stationary techniques. TCS is a broadly-used biocide, also employed in a series of industrial products as a multifunctional additive. Rf, in the presence of light and oxygen, generates singlet molecular oxygen (O2(1Δg)) and superoxide radical anion (O2[rad]–). Results indicate that TCS quenches the triplet excited state of Rf (3Rf*), O2(1Δg), and O2[rad]–. The reactive rate constant for the interaction TCS-O2(1Δg) is 62-faster in alkaline medium with respect to pH 7. Photosensitized degradation of TCS by Rf was much faster than for phenol, a model pollutant, in similar conditions of pH. Kinetic analysis indicated that the reaction of TCS with 3Rf* and/or O2[rad]– is the prevailing oxidative route. Based on the environmental importance of the TCS, the products were determined by UHPLC-MS / MS analysis.
2,4-dichlorophenoxyacetic acid detection using 2,4- dichlorophenoxyacetic acid α-ketoglutarate dioxygenase
Yongxiang Gu,Knaebel,Korus,Crawford
, p. 1622 - 1627 (1995)
2,4-dichlorophenoxyacetic acid (2,4-D) is possibly the most widely used herbicide. Although not very toxic, cleanup of an inadvertant spill is still necessary. This phenoxy herbicide is degraded by several micro-organisms and bioremediation processes have been proposed. Analytical support for these cleanup techniques usually involves gas chromatography or immunoassays, which are moderately (ELISA assays) to very (GC/MS) expensive. Therefore, it is important to develop a quick, inexpensive, and easy-to-use 2,4-D detection method for use in the field by nonspecialists. Reported here is the construction of a detection plasmid, its introduction into Escherichia coli DH5α, and the application of cell-free extracts of this organism to highly specific 2,4-D detection. -from Authors
Photocatalytic degradation of lindane by polyoxometalates: Intermediates and mechanistic aspects
Antonaraki,Triantis,Papaconstantinou,Hiskia
, p. 119 - 124 (2010)
The photocatalytic degradation of lindane (γ-1,2,3,4,5,6-hexachlorocyclohexane) has been studied in the presence of the polyoxometalate PW12O403- in aqueous solutions. Lindane is fully decomposed to CO2, Cl- and H2O, while a great variety of intermediates has been detected using GC-MS, including aromatic compounds (dichlorophenol, trichlorophenols, tetrachlorophenol, hexachlorobenzene, di- and trichloro-benzenodiol), non-aromatic cyclic compounds (penta-, tetrachlorocyclohexene, heptachlorocyclohexane), aliphatic compounds (tetrachloroethane) and condensation products (polychlorinated biphenyls). The number and nature of the intermediates implies that the mechanism of decomposition of lindane is based on both oxidative and reductive processes. Common intermediates have been reported during photolysis of lindane in the presence of titanium dioxide. A similar overall mechanism of polyoxometalates and TiO2 photocatalysis through the formation of common reactive species is suggested.
Charge transfer and photocatalytic activity in CuO/TiO2 nanoparticle heterojunctions synthesised through a rapid, one-pot, microwave solvothermal route
Moniz, Savio J. A.,Tang, Junwang
, p. 1659 - 1667 (2015)
Rapid charge carrier recombination is a major limiting factor over efficiency in many semiconductor photocatalysts. To address this, copper(II) oxide/titanium dioxide (CuO/TiO2) heterojunctions were synthesised through a novel, rapid solvothermal microwave procedure using a low-cost copper precursor and commercial P25 TiO2, taking as little as five minutes to synthesise well-defined CuO nanoparticles onto the host TiO2, achieving an intimate contact. The resultant composites encompass pure CuO particles of approximately 6-7 nm diameter, confirmed by means of high resolution transmission electron microscopy and X-ray photoelectron spectroscopy analysis. Photoelectrochemical water splitting was enhanced by nearly 2 times using the junction, whilst ≈1.6 times enhancement in the photocatalytic mineralisation of a model organic pollutant 2,4-dichlorophenoxyacetic acid (2,4-D) was observed. Furthermore, we studied the initial decomposition mechanism of 2,4-D by means of GC-MS analysis. The increase in catalytic activity, investigated by impedance analysis (Mott-Schottky plots) and photoluminescence spectra, is attributed to photoelectron transfer from the more negative conduction band (CB) of TiO2 to CuO, leaving the photohole on TiO2 to take part in oxidation reactions. This strategy allows for in situ charge separation which facilitates superior photocatalytic activity for both pollutant degradation and water splitting.
Oxidative degradation of toxic organic pollutants by water soluble nonheme iron(iv)-oxo complexes of polydentate nitrogen donor ligands
Jana, Rahul Dev,Munshi, Sandip,Paine, Tapan Kanti
, p. 5590 - 5597 (2021/05/04)
The ability of four mononuclear nonheme iron(iv)-oxo complexes supported by polydentate nitrogen donor ligands to degrade organic pollutants has been investigated. The water soluble iron(ii) complexes upon treatment with ceric ammonium nitrate (CAN) in aqueous solution are converted into the corresponding iron(iv)-oxo complexes. The hydrogen atom transfer (HAT) ability of iron(iv)-oxo species has been exploited for the oxidation of halogenated phenols and other toxic pollutants with weak X-H (X = C, O, S,etc.) bonds. The iron-oxo oxidants can oxidize chloro- and fluorophenols with moderate to high yields under stoichiometric as well as catalytic conditions. Furthermore, these oxidants perform selective oxidative degradation of several persistent organic pollutants (POPs) such as bisphenol A, nonylphenol, 2,4-D (2,4-dichlorophenoxyacetic acid) and gammaxene. This work demonstrates the utility of water soluble iron(iv)-oxo complexes as potential catalysts for the oxidative degradation of a wide range of toxic pollutants, and these oxidants could be considered as an alternative to conventional oxidation methods.
Method for hydrolyzing diarylether compound to generate aryl phenol compound
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Paragraph 0157-0161, (2021/09/29)
The invention discloses a method for hydrolyzing a diarylether compound to generate an arylphenol compound. According to the method, visible light is utilized to excite a photosensitizer for catalysis. In a reaction solvent, the raw material in the formula (1) breaks a C (sp2)-O bond under the auxiliary action of acid, and hydrolysis is performed to obtain the bimolecular aryl phenol compounds in the formula (3) and the formula (4). The method can catalyze the reaction at room temperature, is green and environment-friendly, and is easy to operate; the universality is wide, the reaction yield is relatively high, and the tolerance of functional groups is strong; the synthesis method not only can realize small-scale hydrolysis conversion of various diarylether compounds, but also can realize hydrolysis of herbicidal ether, triclosan and a lignin template substrate, and even can realize large-scale hydrolysis of triclosan and the lignin template substrate to realize gram-level degradation. A new strategy is provided for recovering phenol derivatives through lignin hydrolysis, degrading pesticides and purifying wastewater containing a degerming agent or herbicide. The method has wide application prospect and use value.