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1.
J Phys Chem A ; 119(31): 8519-26, 2015 Aug 06.
Artículo en Inglés | MEDLINE | ID: mdl-26153795

RESUMEN

We report measurements of the product yield for nitryl chloride (ClNO2) production following the reactive uptake of dinitrogen pentoxide (N2O5) to a wide variety of ambient seawater samples as well as seawater mimics. The ClNO2 yield, as measured for ambient seawater collected from both coastal and open ocean waters, was found to be both insensitive to chlorophyll-a, a marker for biological activity, and significantly lower (0.16-0.30) than that expected for equivalent salt-containing solutions (0.82 ± 0.05). Suppression in the ClNO2 yield can be induced by the addition of aromatic organic compounds (e.g., phenol and humic acid) to synthetic seawater matrices. In the case of phenol, surface tension measurements reveal that the surface phenol:chloride ratio can be enhanced by more than a factor of 100 as compared to bulk ratios for subtle changes in surface tension (<1.5 mN m(-1)), providing a mechanism to suppress ClNO2 production at low bulk phenol concentrations. We interpret measurements of the dependence of the ClNO2 yield on phenol using a kinetic model, where we confine the surface enhancement in phenol to the top 1 nm of the interface. Our results are most consistent with a model where N2O5 is ionized within the first three water monolayers (<1 nm), where the product nitronium ions react rapidly with interfacial phenol molecules. These results suggest that ClNO2 may not be formed at the air-sea interface at the yield expected for NaCl, and that the reactive uptake of N2O5 and the subsequent product yield of ClNO2 may serve as a unique probe for the composition of the interfacial region of the sea surface microlayer.

2.
Chem Phys Lett ; 243(3-4): 222-8, 1995 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-11540427

RESUMEN

Molecular dynamics calculations of the scattering of D2O from the glycerol surface at different collision energies are reported. The results for the trapping probabilities and energy transfer are in good agreement with experiments. The calculations demonstrate that the strong attractive forces between these two strongly hydrogen bonding molecules have only a minor effect on the initial collision dynamics. The trapping probability is influenced to a significant extent by the repulsive hard sphere-like initial encounter with the corrugated surface and, only at a later stage, by the efficiency of energy flow in the multiple interactions between the water and the surface molecules.


Asunto(s)
Glicerol/química , Modelos Químicos , Agua/química , Fenómenos Químicos , Química Física , Transferencia de Energía , Enlace de Hidrógeno , Cinética
3.
Science ; 252(5011): 1421-4, 1991 Jun 07.
Artículo en Inglés | MEDLINE | ID: mdl-17772917

RESUMEN

By means of controlled collisions of atoms and molecules with liquid surfaces, molecular beam experiments can be used to probe how gases stick to, rebound from, and exchange energy with molecules in the liquid phase. This report describes measurements of energy exchange in collisions between gases (neon, xenon, and sulfur hexafluoride) and polyatomic liquids (squalane and perfluoropolyether). Energy transfer depends critically on liquid composition and is more efficient for the hydrocarbon than for the perfluorinated ether.

4.
Ann Neurol ; 5(3): 262-7, 1979 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-443758

RESUMEN

Three children with bullous erythema multiforme and 1 with toxic epidermal necrolysis associated with antiepileptic drug therapy are described. One patient is unique because of seven mucocutaneous eruptions caused by three classes of antiepileptic drugs. Lymphocyte stimulation by antiepileptic drugs could not be demonstrated in the 2 patients in whom appropriate studies were performed, and no precipitating antibodies to antiepileptic drugs were found. Observation of four diagnostic and therapeutic principles, which are illustrated by the course of our patients, may reduce the incidence of life-threatening mucocutaneous eruptions and simplify the long-term management of individuals in whom such reactions occur.


Asunto(s)
Anticonvulsivantes/efectos adversos , Eritema Multiforme/inducido químicamente , Síndrome de Stevens-Johnson/etiología , Carbamazepina/efectos adversos , Niño , Preescolar , Eritema Multiforme/inmunología , Femenino , Humanos , Masculino , Mefenitoína/efectos adversos , Fenobarbital/efectos adversos , Fenitoína/efectos adversos , Primidona/efectos adversos , Síndrome de Stevens-Johnson/inmunología
6.
J Exp Zool ; 192(1): 1-12, 1975 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-1092806

RESUMEN

The mechanism and site of teratogenic action of trypan blue on mammalian embryos was reinvestigated. The experiments to be presented include (1) an analysis of the effect of trypan blue treatment on the morphology of the early mouse egg cylinder, (2) a demonstration of the effect of dye treatment on the enzyme acid phosphatase of yolk sac epithelium using histochemical procedures. Results obtained from these experiments indicate that trypan blue injected into mothers on day 7 of gestational age leads, within 12 to 24 hours after treatment, to dramatic abnormalities in 90-95% of egg cylinders examined. The frequency of gross malformations obtained by this treatment is considerably less when litters are examined at later stages of gestation. Acid phosphatase activity in yolk sac epithelium is depressed by the dye treatment, but there is no difference between enzymatically depressed yolk sacs of malformed embryos and yolk sacs surrounding normally appearing litter mates both obtained from trypan blue treated mothers. The hypothesis that trypan blue may exert its teratogenic effect by the direct exposure of egg cylinder stages to the dye, and that some of the egg cylinders affected may subsequently repair, is recommended for further testing.


Asunto(s)
Teratógenos , Azul de Tripano/farmacología , Anomalías Inducidas por Medicamentos , Fosfatasa Ácida/metabolismo , Animales , Epitelio/efectos de los fármacos , Epitelio/enzimología , Femenino , Hematoma/inducido químicamente , Histocitoquímica , Inyecciones Intraperitoneales , Ratones , Microcefalia/inducido químicamente , Morfogénesis/efectos de los fármacos , Disrafia Espinal/inducido químicamente , Azul de Tripano/administración & dosificación , Membrana Vitelina/efectos de los fármacos , Membrana Vitelina/enzimología
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