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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
151

Microfluidic-Based In-Situ Functionalization for Detection of Proteins in Heterogeneous Immunoassays

Asiaei, Sasan January 2013 (has links)
One the most daunting technical challenges in the realization of biosensors is functionalizing transducing surfaces for the detection of biomolecules. Functionalization is defined as the formation of a bio-compatible interface on the transducing surfaces of bio-chemical sensors for immobilizing and subsequent sensing of biomolecules. The kinetics of functionalization reactions is a particularly important issue, since conventional functionalization protocols are associated with lengthy process times, from hours to days. The objective of this thesis is the improvement of the functionalization protocols and their kinetics for biosensing applications. This objective is realized via modeling and experimental verification of novel functionalization techniques in microfluidic environments. The improved functionalization protocols using microfluidic environments enable in-situ functionalization, which reduces the processing times and the amount of reagents consumed, compared to conventional methods. The functionalization is performed using self-assembled monolayers (SAMs) of thiols. The thiols are organic compounds with a sulphur group that assists in the chemisorption of the thiol to the surface of metals like gold. The two reactions in the functionalization process examined in this thesis are the SAM formation and the SAM/probe molecule conjugation. SAM/probe molecule conjugation is the chemical treatment of the SAM followed by the binding of the probe molecule to the SAM. In general, the probe molecule is selective in binding with a given biomolecule, called the target molecule. Within this thesis, the probe molecule is an antibody and the target molecule is an antigen. The kinetics of the reaction between the probe (antibody) and the target biomolecule (antigen) is also studied. The reaction between an antigen and its antibody is called the immunoreaction. The biosensing technique that utilizes the immunoreaction is immunoassay. A numerical model is constructed using the finite element method (FEM), and is used to study the kinetics of the functionalization reactions. The aim of the kinetic studies is to achieve both minimal process times and reagents consumption. The impact of several important parameters on the kinetics of the reactions is investigated, and the trends observed are explained using kinetic descriptive dimensionless numbers, such as the Damköhler number and the Peclet number. Careful numerical modeling of the reactions contributes to a number of findings. A considerably faster than conventional SAM formation protocol is predicted. This fast-SAM protocol is capable of reducing the process times from the conventional 24-hours to 15 minutes. The numerical simulations also predict that conventional conjugation protocols result in the overexposure of the SAM and the probe molecule to the conjugation reagents. This overexposure consequently lowers conjugation efficiencies. The immunoreaction kinetics of a 70 kilo-Dalton heat shock protein (HSP70) with its antibody in a hypothetical microchannel is also investigated through the FEM simulations. Optimal reaction conditions are determined, including the flow velocity and the surface concentration of the immobilized probes (antibodies). Based on the numerical results and a series of experimental studies, the fast-SAM protocol application is successfully confirmed. Moreover, the optimum reagent concentration for a given one- hour conjugation process time is determined. This functionalization protocol is successfully applied to immobilize the HSP70 antibody on gold surfaces. The use of the fast-SAM protocol and the predicted optimum conjugation conditions result in binding of the HSP70 antibody on gold, with the same or superior immobilization quality, compared to the conventional protocols. Upon implementation of a 70 μm.s^(-1) flow velocity, the reaction is observed to complete in around 30-35 minutes, which is close to the numerically predicted 30 minutes and 16 seconds. This immunoreaction time is considerably less than conventional 4-12 hour processes. The modified in-situ functionalization techniques achieved here are promising for substantially reducing the preparation times and improving the performance of biosensors, in general, and immunoassays, in particular.
152

Catalyzed hydrogenation of nitrogen and ethylene on metal (Fe, Pt) single crystal surfaces and effects of coadsorption A sum frequency generation vibrational spectroscopy study.

Westerberg, Staffan Per Gustav January 2004 (has links)
Thesis (Ph.D.); Submitted to the University of California, Berkeley, Berkeley, California (US); 15 Dec 2004. / Published through the Information Bridge: DOE Scientific and Technical Information. "LBNL--56814" Westerberg, Staffan Per Gustav. USDOE Director. Office of Science. Office of Basic Energy Sciences (US) 12/15/2004. Report is also available in paper and microfiche from NTIS.
153

Sintese e marcacao com P-32 de fosfatos de monoalquila e do fosfato de monofenila sob forma de sais de bis-ciclohexilamonio. Determinacao de espectros de absorcao em infra-vermelho e de ressonancia nuclear magnetica

ALMEIDA, MARIA A.T.M. de 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:23:11Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:29Z (GMT). No. of bitstreams: 1 00636.pdf: 4746331 bytes, checksum: 49aa6e0eb3bdd9da261862a04bcb4b58 (MD5) / Dissertacao (Mestrado) / IEA/D / Instituto de Quimica, Universidade de Sao Paulo - IQ/USP
154

Estudo morfologico e cinetico da nitretacao por plasma pulsado do aco inoxidavel martensitico AISI 420

PINEDO, CARLOS E. 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:44:26Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:39Z (GMT). No. of bitstreams: 1 06912.pdf: 10380955 bytes, checksum: 3e22ae9dda613db66c72f121ed37b278 (MD5) / Tese (Doutoramento) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP
155

Impact des opérations thermiques agroalimentaires à hautes températures sur la dégradation des anthocyanes : caractérisation et modélisation des cinétiques réactionnelles / Impact of food thermal operations at high temperature on the degradation of anthocyanins : characterization and modeling of reaction kinetics

Jimenez Elizondo, Nadiarid 13 December 2011 (has links)
Compte tenu de l'importance des pigments naturels dans les aliments et leur sensibilité aux traitements thermiques, les cinétiques de dégradation des anthocyanes ont été étudiées à très hautes températures (100 à 180 ºC). Pour obtenir une base de données expérimentale fiable dissociant les transferts d'énergie et de matière, un mini-réacteur étanche a été utilisé pour le traitement d'une matrice modèle (jus de mûre et sable) en faisant varier la température et l'activité de l'eau (0,20<aw<0,99). L'hypothèse d'une réaction d'ordre 1 pour la dégradation des anthocyanes a permis de modéliser et de déterminer les paramètres cinétiques suivant une méthode non-isotherme prenant en compte à la fois le profil de température et indépendamment l'homogénéité ou l'hétérogénéité du champs de température au sein de la matrice. Il a été démontré que les constantes de réaction sont très influencées par la diminution de l'activité de l'eau, facteur qui fait augmenter la réactivité. Ces résultats originaux ont été validés sur une matrice alimentaire (papaye verte-jus de mûre) soumise au couplage d'un procédé de formulation par déshydratation par immersion-imprégnation, suivi d'une opération de friture, à l'aide d'un modèle qui intègre les transferts de vapeur et d'énergie et la cinétique réactionnelle. Le modèle permet une meilleure compréhension des phénomènes et il peut être intégré dans une démarche d'optimisation séquentielle associant différentes opérations unitaires avec des traitements thermiques à très hautes températures. / Given the importance of natural pigments in foods and their sensitivity to heat treatment, degradation kinetics of anthocyanins have been studied at very high temperatures (100 to 180 ºC). For a reliable experimental database that dissociates heat and mass transfer, a hermetic mini-reactor was used for the treatment of a model matrix (blackberry juice and sand) by varying the temperature and activity water (0.20<aw<0.99). The assumption of a first order reaction for the anthocyanins degradation was used to model and determine the kinetic parameters using a non-isothermal method taking into account both the temperature profile and independently the homogeneity or heterogeneity of the matrix temperature field. It has been shown that the rate constants are strongly influenced by the water activity reduction, a factor that increases the anthocyanins reactivity. These original results were validated on a food matrix (green papaya-blackberry juice) submitted to the coupling of a formulation process by osmotic dehydration, followed by a deep-fat frying operation, using a model which includes the vapor and heat transfer and the reaction kinetics. The model allows a better understanding of the phenomena and can be integrated into a sequential optimization approach combining different unit operations with heat treatments at high temperatures.
156

Obtenção de reatividade subcrítica por meio de medidas de APSD e CPSD utilizando detectores modo pulso no reator IPEN/MB-01 / Obtainment of subcritical reactivity by mean of measurement of APSD and CPSD employing pulse mode detectors in the IPEN/MB-01 reactor

LEE, SEUNG M. 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:42:36Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:02:07Z (GMT). No. of bitstreams: 0 / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / Tese (Doutorado em Tecnologia Nuclear) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP / FAPESP:09/54838-0
157

Estudo comparativo sobre a adsorção de diferentes classes de corantes em zeólitas de cinzas de carvão: modelagem cinética e de equilíbrio / Comparative study on the adsorption of different classes of dyes in zeolites of coal ashes: kinetic and equilibrium modellig

BERTOLINI, THARCILA C.R. 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:41:55Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:07:16Z (GMT). No. of bitstreams: 0 / Dissertação (Mestrado) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
158

Influência de um revestimento de nióbio sobre a resistência à simulação das ligas FeCr e FeCrY / Influence niobium coating on sulfidation resistance of FeCr and FeCrY alloys

GERIBOLA, GUILHERME A. 24 February 2015 (has links)
Submitted by Maria Eneide de Souza Araujo (mearaujo@ipen.br) on 2015-02-24T18:21:24Z No. of bitstreams: 0 / Made available in DSpace on 2015-02-24T18:21:24Z (GMT). No. of bitstreams: 0 / Dissertação (Mestrado em Tecnologia Nuclear) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
159

Estudo morfologico e cinetico da nitretacao por plasma pulsado do aco inoxidavel martensitico AISI 420

PINEDO, CARLOS E. 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:44:26Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:39Z (GMT). No. of bitstreams: 1 06912.pdf: 10380955 bytes, checksum: 3e22ae9dda613db66c72f121ed37b278 (MD5) / Tese (Doutoramento) / IPEN/T / Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP
160

Sintese e marcacao com P-32 de fosfatos de monoalquila e do fosfato de monofenila sob forma de sais de bis-ciclohexilamonio. Determinacao de espectros de absorcao em infra-vermelho e de ressonancia nuclear magnetica

ALMEIDA, MARIA A.T.M. de 09 October 2014 (has links)
Made available in DSpace on 2014-10-09T12:23:11Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T13:56:29Z (GMT). No. of bitstreams: 1 00636.pdf: 4746331 bytes, checksum: 49aa6e0eb3bdd9da261862a04bcb4b58 (MD5) / Dissertacao (Mestrado) / IEA/D / Instituto de Quimica, Universidade de Sao Paulo - IQ/USP

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