4911-70-0Relevant articles and documents
Zeolite 4A supported CdS/g-C3N4 type-II heterojunction: A novel visible-light-active ternary nanocomposite for potential photocatalytic degradation of cefoperazone
AttariKhasraghi, Naime,Behnajady, Mohammad A.,Mehrizad, Ali,Modirshahla, Nasser,Zare, Karim
, (2021/09/15)
The CdS/g-C3N4 heterojunction photocatalyst supported on 4A zeolite was successfully synthesized using a simple chemical precipitation method. The physicochemical characteristics of the as-prepared ternary composite were assessed using X-Ray diffraction (XRD), field emission- scanning electron microscopy (FE-SEM), energy dispersive X-Ray (EDX), transmission electron microscopy (TEM), N2 adsorption–desorption, differential reflectance spectroscopy (UV–Vis-DRS), and photoluminescence (PL) techniques. The results confirmed the successful synthesis of the CdS/g-C3N4/4AZ nanocomposite and introduction of the CdS and g-C3N4 on the substrate of 4A zeolite. Cefoperazone (CFP) antibiotic was tested as the model pollutant to assess the photocatalytic performance of the synthesized nanocomposite under visible light irradiation. The response surface methodology (RSM) and artificial neural network (ANN) showed desirable reasonability for the prediction of the CFP degradation efficiency. More than 93% of CFP with a concentration of 17 mg L-1 degraded in the presence of the 0.4 g L-1 of the catalyst at pH of 9 after 80 min treatment time (RSM-based optimization results). The pH of the solution, irradiation time, catalyst dosage, and the initial concentration of the CFP affected degradation efficiency with a percentage impact of 37, 29, 19, and 15 %, respectively (ANN-based modeling results). The addition of 1 mM of isopropanol, benzoquinone, and sodium oxalate reduced the CFP degradation efficiency from 93.23% to 85.18, 41.16, and 32.47%, respectively, proving the decisive role of the °O2– and h+ in the photodegradation process. The kinetic studies indicated the following of the process from the Langmuir-Hinshelwood's pseudo-first-order model (kapp = 3.71 × 10-2 min?1). The structure of the identified by-products using GC-MS analysis confirmed that CFP mainly decomposed through the cleavage of C-S, C-N, and N-N bonds. Moreover, the formation of the aliphatic compounds and carboxylic acids as by-products confirmed nearly complete mineralization of the CFP to non-toxic products.
Stereochemistry of Aliphatic Carbocations, 12. Alkyl Shifts between Secondary Carbon Atoms
Kirmse, Wolfgang,Prolingheuer, Ernst-Christoph
, p. 104 - 128 (2007/10/02)
Several optically active, β-branched alkylamines have been synthesized from amino acids.The corresponding amines were obtained from isobutyraldehyde and 2-methylbutanal (37), respectively.The stereochemistry at the terminus of 1,2-methyl shifts has been elucidated in the nitrous acid deaminations of 4 and 21.Predominant, although incomplete inversion at the migration terminus is consistent with conformational control rather than neighboring group participation.The deamination of 31 involves a degenerate 1,2-ethyl shift and a nondegenerate 1,2-methyl shift, the reverse holds for 44.Complete inversion at the origin of the methyl migrations and the absence of subsequent retrogressive H shifts strongly support the intermediacy of methyl-bridged carbocations.Partial racemization at the origin of the ethyl migrations has been traced to proton shifts within ethyl-bridged intermediates.Rearranged open cations contribute significantly to the overall reaction if micelles are produced by self-aggregation of the alkylammonium ions.
Stereochemistry of Aliphatic Carbocations, 14. Alkyl Shifts from Secondary to Primary Carbon Atoms
Kirmse, Wolfgang,Guenther, Bernd-Rainer,Knist, Johannes,Kratz, Sigrid,Loosen, Karin,et al.
, p. 2127 - 2139 (2007/10/02)
Alkyl shifts from secondary to primary carbon atoms have been induced by the nitrous acid deamination of suitable amines (4, 22, 39, 51); they include sequential rearrangements (-CH3,CH3 and -CH3,H).Predominant although incomplete inversion at the migration origin has been observed (Me 70percent, Et 62-64percent, nPr 65percent, iPr 64percent, tBu 55percent).Our results require the intervention of open secondary carbocations which may be preceded by less stable bridged intermediates.
