Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Adv Sci (Weinh) ; 10(29): e2303407, 2023 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-37525629

RESUMEN

The main obstacle of ionic thermo-electrochemical cells (TECs) in continuous power supply lies in a low heat-to-electricity energy conversion efficiency because most TECs work in thermodiffusion mode in which the ions are confined in a liquid/electrolyte media. The introduction of the redox couple onto the electrode surface may overcome the obstacle by resolving the low mass transport rate of ions caused by the redox process occurring near but not on the electrode surface. Herein, the authors demonstrate enhancement of TECs by integrating the redox couple directly onto the electrode surface to maximize the mass transport efficiency. A discontinuous interfacial modification strategy is developed by using a carbon cloth/iron (II/III) phytate as the symmetric electrodes. The gelled electrolyte consisting of a polyacrylamide matrix and phytic acid is shown to promote selective ion diffusion. A synergistic combination consisting of the thermodiffusion effect and redox reactions on the electrode is established in a pre-treated layout. Such TEC affords a high output voltage of 0.4 V, an excellent instantaneous output power density (20.26 mW m-2 K-2 ) and a record-high 2 h output energy density (2451 J m-2 ) under TH = 30 °C with TC = 15 °C, with an ultrahigh Carnot-relative efficiency of 1.12%.

2.
J Org Chem ; 88(5): 2898-2907, 2023 Mar 03.
Artículo en Inglés | MEDLINE | ID: mdl-36802599

RESUMEN

An efficient triflic anhydride promoted phosphorylation of ketone was disclosed, and vinylphosphorus compounds were prepared under solvent- and metal-free conditions. Both aryl and alkyl ketones could perform smoothly to give vinyl phosphonates in high to excellent yields. In addition, the reaction was easy to carry out and easy to scale up. Mechanistic studies suggested that this transformation might involve nucleophilic vinylic substitution or a nucleophilic addition-elimination mechanism.

3.
J Am Chem Soc ; 144(37): 16953-16964, 2022 09 21.
Artículo en Inglés | MEDLINE | ID: mdl-36070362

RESUMEN

Organosulfates (OSs) are well-known and ubiquitous constituents of atmospheric aerosol particles and have been used as secondary organic aerosol markers in many field studies. Hence, it is imperative to understand the formation of OS species in the atmosphere. Recently, hydroxy acids (HAs) and hydroxy acid sulfates have been extensively detected in the atmospheric environment. However, the reaction mechanism of HAs to form OSs is much less understood. In this work, we have mainly investigated the reaction of typical α-HAs, including glycolic acid (GA) and lactic acid (LA), and SO3 at the liquid aerosol surface using quantum chemistry calculations and Born-Oppenheimer molecular dynamics simulations. The OH group orientation of α-HAs at the air-water interface is found to exert a significant impact on the formation of OSs. The OH group pointing to the gas phase is obviously beneficial to the formation of OSs. Two key factors are discovered important to the reaction of α-HAs adsorbed on the liquid surface with SO3: (a) the exposure position of the active site to the gas phase and (b) the reactivity of the exposed site to the attracted SO3 molecule. Moreover, we found that the air-water interface exerts a significant influence on the physicochemical behaviors of GA and LA, especially on their OH group orientation, and thus leads to their different properties for the SO3 colliding reaction. The presented reaction mechanism provides a new feasible pathway for the production of OSs at the liquid aerosol surface, which may have important impacts on the formation of organic aerosols.


Asunto(s)
Sulfatos , Agua , Aerosoles/química , Hidroxiácidos , Ácido Láctico , Sulfatos/química
4.
Sensors (Basel) ; 21(21)2021 Oct 29.
Artículo en Inglés | MEDLINE | ID: mdl-34770495

RESUMEN

Based on the principle of underwater transducers, an ultrasonic four-laminated transducer with a frequency of 1 MHz was proposed to solve the problem of large energy attenuation when ultrasonic waves propagate in viscoelastic media. First, this study targeted solid rocket propellant as the research object, and the energy attenuation characteristics of ultrasonic waves propagating in viscoelastic media were analyzed through the derivation of the wave equation. Second, the structure of a four-laminated transducer with a frequency of 1 MHz was designed, and the resonance frequency was obtained by a graphical method. The sound field simulation and experimental results showed that the gain of the four-laminated transducer was 15 dB higher than that of the single-wafer transducer. An ultrasonic feature scanning system was built to complete the qualitative and quantitative detection of the smallest artificial hole (ϕ2 mm × 10 mm). Finally, two different natural defects were scanned, and the results were compared with those obtained using an industrial computed tomography detection system. The results showed that the ultrasonic method was more accurate in characterizing two natural defects. The primary cause was that the industrial CT was not sensitive to defects parallel to the incident direction of the ray. Therefore, this study not only achieved the qualitative and quantitative nondestructive testing of solid rocket propellants, but also provides an important reference for other viscoelastic components.


Asunto(s)
Transductores , Ultrasonido , Simulación por Computador , Sonido , Vibración
5.
RSC Adv ; 11(40): 24991-24994, 2021 Jul 13.
Artículo en Inglés | MEDLINE | ID: mdl-35481042

RESUMEN

An addition of H-phosphonates to aryl alkynes was realized under solvent- and metal-free conditions, affording Markovnikov-selective α-vinylphosphonates in moderate to good yields. A wide range of aryl alkynes could be applied for the reaction. A tentative mechanism of addition-substitution was proposed based on in situ 31P {1H} NMR studies.

SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA