Search results for " transfer"

showing 10 items of 3683 documents

Information Decomposition in Bivariate Systems: Theory and Application to Cardiorespiratory Dynamics

2015

In the framework of information dynamics, the temporal evolution of coupled systems can be studied by decomposing the predictive information about an assigned target system into amounts quantifying the information stored inside the system and the information transferred to it. While information storage and transfer are computed through the known self-entropy (SE) and transfer entropy (TE), an alternative decomposition evidences the so-called cross entropy (CE) and conditional SE (cSE), quantifying the cross information and internal information of the target system, respectively. This study presents a thorough evaluation of SE, TE, CE and cSE as quantities related to the causal statistical s…

causalityInformation dynamicsTransfer entropyDynamical systems theoryComputationGeneral Physics and Astronomylcsh:AstrophysicsBivariate analysisMultivariate autoregressive processeMachine learningcomputer.software_genreMultivariate autoregressive processesCardiorespiratory interactionsPhysics and Astronomy (all)Systems theoryDynamical systemslcsh:QB460-466Decomposition (computer science)Statistical physicslcsh:ScienceCardiorespiratory interactions; Causality; Dynamical systems; Heart rate variability; Information dynamics; Multivariate autoregressive processes; Transfer entropyHeart rate variabilityMathematicsCardiorespiratory interactions; Causality; Dynamical systems; Heart rate variability; Information dynamics; Multivariate autoregressive processes; Transfer entropy; Physics and Astronomy (all)business.industryCardiorespiratory interactionheart rate variabilitytransfer entropyDynamical systemcardiorespiratory interactionsdynamical systemslcsh:QC1-999CausalityInformation dynamicCross entropySettore ING-INF/06 - Bioingegneria Elettronica E Informaticamultivariate autoregressive processesBenchmark (computing)lcsh:QTransfer entropyArtificial intelligenceinformation dynamicsbusinesscomputerlcsh:PhysicsEntropy
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The use of morphokinetics as a predictor of embryo implantation.

2011

Background Time-lapse observation presents an opportunity for optimizing embryo selection based on morphological grading as well as providing novel kinetic parameters, which may further improve accurate selection of viable embryos. The objective of this retrospective study was to identify the morphokinetic parameters specific to embryos that were capable of implanting. In order to compare a large number of embryos, with minimal variation in culture conditions, we have used an automatic embryo monitoring system. Methods Using a tri-gas IVF incubator with a built-in camera designed to automatically acquire images at defined time points, we have simultaneously monitored up to 72 individual emb…

cell divisionAdultMalemedicine.medical_specialtyBlastomeresTime FactorsCell divisiontime-lapseCleavage Stage OvumEnvironment controlledFertilization in VitroBiologyCleavage (embryo)AndrologyPregnancymedicineHumansEmbryo ImplantationSperm Injections IntracytoplasmicRetrospective StudiesRehabilitationPregnancy OutcomeObstetrics and GynecologyEmbryoBlastomereCell cycleEmbryo TransferEmbryo transferSurgeryexact timingKineticsReproductive MedicineEmbryoembryonic structuresOocytesFemalepregnancyCytokinesisHuman reproduction (Oxford, England)
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Wireless ATM : handover issues

1998

Basic aspects of cellular systems and the ATM transmission technology are introduced. Wireless ATM is presented as a combination of radio ATM and mobile ATM. Radio ATM is a wireless extension of an ATM connection while mobile ATM contains the necessary extensions to ATM to support mobility. Because the current ATM technology does not support mobility, handover becomes one of the most important research issues for wireless ATM. Wireless ATM handover requirements are thus analysed. A handover solution relying on two inter-related handover protocols is presented and evaluated. Future research is needed to compare this solution with options presented by earlier research and possibly combine the…

cellular radioasynchronous transfer modeComputerSystemsOrganization_COMPUTER-COMMUNICATIONNETWORKSprotocolsmultimedia communicationpacet radio networksradio ATMmultimedia servicesdigital cellular systemsATM transmission technologyhandover issuesdigital radiowireless ATMGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)mobile ATM
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Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. I. Studies of the chain‐transfer rea…

2001

The effect of hydrogen on the molecular weight of polyethylene obtained over vanadium catalysts (based on VCl4 and VOCl3) supported on MgCl2(THF)2 was studied and the results were compared to those obtained for similar titanium catalysts. It was confirmed that the dependencies of the transfer reaction on the hydrogen concentration are a half‐order in all investigated systems. However, the transition metal of the catalytic site affects the ratio of the transfer rate with hydrogen to the propagation rate (ktr,H/kp) and the results showed that hydrogen is a more effective agent of polyethylene molecular weight control in vanadium‐based systems as compared to the titanium catalyst.

chain transfer with hydrogenvanadium and titanium catalystshydrogenmolecular weightethylene polymerizationJournal of Applied Polymer Science
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Synthesis, X-ray structure, Hirshfeld analysis, and DFT studies of a new Pd(II) complex with an anionic s-triazine NNO donor ligand

2020

Abstract A new Pd(II) complex, [Pd(Triaz)Cl], with the hydrazono-s-triazine ligand, 2,4-di-tert-butyl-6-((2-(4-morpholino-6-(phenylamino)-1,3,5-triazin-2-yl)hydrazono)methyl)phenol (HTriaz), was synthesized by the reaction of PdCl2 with the organic ligand (1:1) in acetone under isothermal conditions. The molecular structure of the [Pd(Triaz)Cl] complex was determined using FTIR and 1H NMR spectroscopic techniques, and single-crystal X-ray diffraction. Moreover, using Hirshfeld surface analysis, the percentages of the intermolecular interactions were determined. The obtained values were 60.6%, 11.6%, 8.1%, 3.6%, and 5.0% for the H⋯H, C⋯H, O⋯H, N⋯H, and Cl⋯H interactions, respectively. Among …

chemistry.chemical_classification010405 organic chemistryChemistryLigandOrganic ChemistryIntermolecular forceHydrazone010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographychemistry.chemical_compoundElectron transferProton NMRMoleculeSpectroscopyTriazineNatural bond orbitalJournal of Molecular Structure
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From macroscopic to molecular scale investigations of mass transfer of small molecules through edible packaging applied at interfaces of multiphase f…

2009

Abstract This paper presents a multi-scale approach to investigate mass transfer properties of edible films that integrates some published data and new original results. The transport of small molecules, such as water, between the different parts of multiphase food products leads to quality deterioration and thus requires the use of barrier edible films or coatings. Therefore, it is necessary to characterise the properties of both food and edible barriers, like the diffusivities of their respective migrants. Surface properties characterisation of edible films, composed of an iota-carrageenan matrix in association with a high melting point fat was investigated by goniometry and allows the de…

chemistry.chemical_classificationAbsorption of waterMoisturebusiness.industryAnalytical chemistryFood technologyGeneral ChemistryPolymerPermeationIndustrial and Manufacturing EngineeringFood packagingChemical engineeringchemistryMass transferWettingbusinessFood ScienceInnovative Food Science & Emerging Technologies
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Functionalization and patterning of reactive polymer brushes based on surface reversible addition and fragmentation chain transfer polymerization

2012

We present the synthesis of reactive polymer brushes prepared by surface reversible addition–fragmentation chain transfer polymerization of pentafluorophenyl acrylate. The reactive ester moieties can be used to functionalize the polymer brush film with virtually any functionality by simple post-polymerization modification with amines. Dithiobenzoic acid benzyl-(4-ethyltrimethoxylsilyl) ester was used as the surface chain transfer agent (S-CTA) and the anchoring group onto the silicon substrates. Reactive polymer brushes with adjustable molecular weight, high grafting density, and conformal coverage through the grafting-from approach were obtained. Subsequently, the reactive polymer brushes …

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryChain transferPolymerPolymer brushchemistry.chemical_compoundchemistryChemical engineeringPolymerizationPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationWettingJournal of Polymer Science Part A: Polymer Chemistry
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Substrate-Independent Stable and Adherent Reactive Surface Coatings and their Conversion with Amines

2007

To create stable, adherent and reactive surface coatings, a hybrid polymer composed of poly(methylsilsesquioxane) (PMSSQ) and poly(pentafluorophenyl acrylate) PFPA with a M n of 32000 g/mol was prepared by a RAFT polymerization procedure. These hybrid polymer has been used for coating experiments. The PFPA part enabled a variable functionalization of the coating afterwards. The stability on various substrates (e.g. glass, PMMA, steel) was tested in an ISO tape test. These reactive surface coatings were modified using different amines, such as amino-terminated PEG, dodecyl amine and N-isopropyl amine. The conversion was analyzed by FT-IR and contact angle measurements.

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryChain transferPolymerengineering.materialCondensed Matter PhysicsContact anglechemistry.chemical_compoundCoatingchemistryPolymer chemistryMaterials ChemistryengineeringSurface modificationThermal stabilityReversible addition−fragmentation chain-transfer polymerizationMacromolecular Symposia
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Core-shell polyacrylate and polystyrene-block-polyacrylate stars

2005

The polymerization of p-(iodomethyl)styrene (PIMS) yields well-defined branched polymers with reactive iodomethyl groups. The branched poly[p-(iodomethyl)styrene] was used as the transfer agent in the iodine mediated radical polymerization of vinyl monomers. The polymerization proceeds in a controlled way and yields polystyrene and poly(t-butyl acrylate) star polymers with reactive groups at the end of their arms. Polymers so obtained were also used to prepare stars with block copolymer arms: polystyrene-block-poly(t-butyl acrylate). The characterization of star structures was performed by NMR and gel permeation chromatography with absolute molar mass detection (MALLS). Preliminary characte…

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferPolymerStyrenechemistry.chemical_compoundPolymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerPolystyrenePolymer
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Transfer to Polymer and Long-Chain Branching in PLP-SEC of Acrylates

2009

Pulsed laser polymerization (PLP) combined with size exclusion chromatography (SEC) is the method of choice for determining propagation rate coefficients. The influence of the long-chain branching in PLP-SEC is investigated using multiple-detection SEC and a recently developed method to detect long-chain branching [P. Castignolles, R. Grab, M. Parkinson, M. Wilhelm, M. Gaborieau, Polymer 2009, 50, 2373.] While little or no long-chain branching is detected in poly(n-butyl acrylate), the error in relevant molecular weights of poly(2-ethylhexyl acrylate) is large (30-100%) due to long-chain branching. Possible variations of propagation rate coefficient with alkyl groups in alkyl acrylates or w…

chemistry.chemical_classificationAcrylatePolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationSize-exclusion chromatographySolution polymerizationChain transferBranching (polymer chemistry)chemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryAlkylMacromolecular Rapid Communications
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