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1.
J Chromatogr A ; 1458: 126-35, 2016 Aug 05.
Artigo em Inglês | MEDLINE | ID: mdl-27378248

RESUMO

The partial oxidation of isobutane to t-butyl hydroperoxide (TBHP) has been studied analytically for the first time as a two-phase process in a capillary micro reactor. In order to obtain detailed information on products, yields, selectivities and reaction pathways, the products have been investigated by GC/MS. An Rxi-5ms column and a PTV-injector have been used to analyze the liquid products. TBHP, di-t-butyl peroxide (DTBP), t-butanol (TBA), and propanone as main products as well as further by-products e.g. methanal, isopropanol, isobutanol and isobutanal in minor quantities have been identified by MS. The liquid products have been obtained by quenching the reaction and vaporizing the isobutane afterwards by pressure reduction using a mass flow controller allowing a constant mass flow. For all liquid reaction products calibrations, a validation of the method including limits of quantification and detection as well as calculation of uncertainties has been performed. The results have been applied successfully for the investigation of the selectivities of the main products (TBHP, DTBP, TBA, propanone) of the isobutane oxidation. In the frame of the analytical investigation of this reaction a correlation coefficient of r(2)>0.999 for TBHP and DTBP, which is necessary to perform a validation, has been obtained for the first time. The gaseous phase has been analyzed using a GASPRO column, a DEANS switch, a mole sieve column and a TCD detector. Apart from the gaseous reactants, isobutene has been found.


Assuntos
Butanos/química , Cromatografia Gasosa-Espectrometria de Massas/métodos , Butanóis/análise , Butanóis/química , Gases/análise , Gases/química , Oxirredução , Peróxidos/análise , Peróxidos/química , Pressão , Propano/análogos & derivados , Propano/análise , Propano/química , Volatilização
2.
ACS Macro Lett ; 2(9): 766-769, 2013 Sep 17.
Artigo em Inglês | MEDLINE | ID: mdl-35606977

RESUMO

We present a novel class of light-responsive particles for fluorescence modulation at low switching doses. The particles also exhibit phase-changing and shape-shifting behavior. The monodisperse conjugated polymer particles with incorporated light-switchable azobenzene moieties are prepared in a Suzuki-Miyaura dispersion polymerization. The influence of the molecular structure and the trans-to-cis switching behavior on the photonic performance are investigated. The polymer particles present ideal candidates for responsive organic photonics and as high resolution marker systems for biomedical applications.

3.
Clin Chem ; 51(10): 1923-32, 2005 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16055433

RESUMO

BACKGROUND: Use of microfluidics in point-of-care testing (POCT) will require on-board fluidics, self-contained reagents, and multistep reactions, all at a low cost. Disposable microchips were studied as a potential POCT platform. METHODS: Micron-sized structures and capillaries were embedded in disposable plastics with mechanisms for fluidic control, metering, specimen application, separation, and mixing of nanoliter to microliter volumes. Designs allowed dry reagents to be on separate substrates and liquid reagents to be added. Control of surface energy to +/-5 dyne/cm2 and mechanical tolerances to < or = 1 microm were used to control flow propulsion into adsorptive, chromatographic, and capillary zones. Fluidic mechanisms were combined into working examples for urinalysis, blood glucose, and hemoglobin A(1c) testing using indicators (substances that react with analyte, such as dyes, enzyme substrates, and diazonium salts), catalytic reactions, and antibodies as recognition components. Optical signal generation characterized fluid flow and allowed detection. RESULTS: We produced chips that included capillary geometries from 10 to 200 microm with geometries for stopping and starting the flow of blood, urine, or buffer; vented chambers for metering and splitting 100 nL to 30 microL; specimen inlets for bubble-free specimen entry and containment; capillary manifolds for mixing; microstructure interfaces for homogeneous transfer into separation membranes; miniaturized containers for liquid storage and release; and moisture vapor barrier seals for easy use. Serum was separated from whole blood in <10 s. Miniaturization benefits were obtained at 10-200 microm. CONCLUSION: Disposable microchip technology is compatible with conventional dry-reagent technology and allows a highly compact system for complex assay sequences with minimum manual manipulations and simple operation.


Assuntos
Hemoglobinas Glicadas/análise , Técnicas Analíticas Microfluídicas/instrumentação , Técnicas Analíticas Microfluídicas/métodos , Microfluídica/instrumentação , Microfluídica/métodos , Glicemia/análise , Desenho de Equipamento , Humanos , Imunoensaio/instrumentação , Sistemas Automatizados de Assistência Junto ao Leito , Sensibilidade e Especificidade , Propriedades de Superfície , Urinálise/instrumentação
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