Search results for "polymerization"

showing 10 items of 1689 documents

Compound Membranes of Linearly Polymerized and Cross-Linked Macrolipids with Phospholipids: Preparation, Microstructure and Applications

1985

Methods for the assembly and for studying the structural and dynamic properties of partially polymerized membranes are described. Mixtures of two classes of polymerizable amphiphiles with diacyl phosphatidylcholines are studied: (1) phosphatidylcholines carrying a diacetylene group per chain (abbreviated as (m,n)-DIINPC (where m + n + 6 equals number of C-Atoms per chain) and (2) a phospholipid-like molecule with a polymerizable methacryl ligand connected to the phosphate head group via (CH2CH2O)m spacers which is abbreviated as (m.n)-POMECY (n = number of C-atoms per chain). — Phase diagrams of the lipid mixtures are established by static light scattering in combination with freeze fractur…

Materials scienceDiacetyleneGeneral Chemical EngineeringVesicleDegree of polymerizationPhotobleachingchemistry.chemical_compoundCrystallographyMonomerMembranechemistryPolymerizationPolymer chemistryStatic light scatteringBerichte der Bunsengesellschaft für physikalische Chemie
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Material transport and organizing phenomena of Langmuir—Blodgett membranes from polymerizable built up diacetylene amphiphiles on hydrophobic supports

1986

Abstract Langmuir—Blodgett multilayers of polymerized diin amphiphiles on different porous, hydrophobic ultrafilters have been studied as composite membranes under the conditions of reverse osmosis. Influences of differently structured surfaces of the supports on structure and phase change occurring during polymerization have been investigated by scanning electron microscopy and X-ray diffraction and are discussed with reverse osmosis data. When conditioned, fine porous hydrophobic supports become permeable to aqueous solutions at low pressures. Under these conditions permeate flux and retention were found to depend on the number of layers deposited.

Materials scienceDiacetyleneScanning electron microscopetechnology industry and agricultureFiltration and SeparationBiochemistryLangmuir–Blodgett filmchemistry.chemical_compoundMembranePhotopolymerchemistryPolymerizationChemical engineeringPolymer chemistryAmphiphileGeneral Materials SciencePhysical and Theoretical ChemistryReverse osmosisJournal of Membrane Science
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Thermal behavior of ethylene copolymers with di- and tri-alkenylsilsesquioxane comonomers synthesized by post-metallocene catalysts

2020

AbstractThis paper reported thermal properties of ethylene copolymers with di- and tri-alkenylsilsesquioxanes (POSS) synthesized by bis(phenoxy-imine) Ti, Zr, V, and V salen-type complexes. Ethylene copolymers with multi-alkenyl POSS obtained by such complexes contain multi-alkenyl POSS incorporated into the polymer chain as a side group. They were characterized by different thermal behavior depending on the kind of multi-alkenyl POSS comonomer, and type of the catalyst used, as well as polymerization conditions and thus the structure of the copolymer chain. Ethylene/POSS copolymers differed in incorporation of POSS into the polymer chain, content of specific unsaturation groups, and molecu…

Materials scienceEthylene02 engineering and technology01 natural scienceschemistry.chemical_compoundEthyleneCopolymerThermal stabilityPhysical and Theoretical ChemistryPendant groupchemistry.chemical_classificationComonomerCopolymersMelting and crystallization processPolymerThermal stability021001 nanoscience & nanotechnologyCondensed Matter Physics010406 physical chemistry0104 chemical scienceschemistryPolymerizationChemical engineeringMulti-alkenyl polyhedral oligomeric silsesquioxanes (POSS)0210 nano-technologyMetalloceneJournal of Thermal Analysis and Calorimetry
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Ethylene/POSS copolymerization behavior of postmetallocene catalysts and copolymer characteristics

2017

Copolymerization of ethylene with iso-butyl substituted monoalkenyl(siloxy)- or monoalkenylsilsesquioxane (POSS) comonomers over bis(phenoxy-imine) and salen-type titanium and zirconium catalysts was studied. It was found that the polyreaction performance was significantly depended by the kind of the catalyst and by the structure and concentration of POSS in the feed. The POSS comonomer was efficiently incorporated into the polymer chain at up to 0.2 mol %. The differences in the copolymer compositions as the functions of the catalyst kind and the POSS comonomer were observed, including the varied number-average sequence length of ethylene and unsaturated end groups, as determined by 1H NMR…

Materials scienceEthylenePolymers and Plasticspolyhedral oligomeric silsesquiox-ane (POSS)02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundCrystallinitylawPolymer chemistryMaterials ChemistryCopolymerThermal stabilitystructureCrystallizationchemistry.chemical_classificationComonomerOrganic ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciencescopolymerizationpostmetallocene catalystchemistry0210 nano-technologythermoplasticsJournal of Polymer Science Part A-Polymer Chemistry
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Organic-inorganic materials through first simultaneous frontal polymerization and frontal geopolymerization

2021

Abstract The first frontal geopolymerization (FGP) took place in the same reaction medium in which the frontal polymerization (FP) of 1,6-hexanediol diacrylate (HDDA) was occurring, thus giving rise to an organic-inorganic hybrid in one step in just a few minutes. Because of their exothermicity, the two reactions support each other and sustain propagating fronts. By contrast, using the classical techniques (prolonged heating) instead of FP, due to large gas formation, the reaction is explosive or, if carried out at room temperature, phase separation occurred.

Materials scienceExplosive materialMechanical EngineeringFrontal polymerizationOne-Step02 engineering and technologyGeopolymer; Frontal polymerization; Frontal geopolymerization; HybridGeopolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsFrontal geopolymerization01 natural sciencesHybrid0104 chemical sciencesGeopolymerFrontal geopolymerization; Frontal polymerization; Geopolymer; HybridPolymerizationGas formationChemical engineeringMechanics of MaterialsOrganic inorganicGeneral Materials Science0210 nano-technologyMaterials Letters
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Electrochemical Fabrication and Physicochemical Characterization of Metal/High-k Insulating Oxide/Polymer/Electrolyte Junctions

2014

Photoelectrochemical polymerization of poly(3,4-ethylenedioxythiophene), PEDOT, was successfully realized on anodic film grown to 50 V on magnetron sputtered Ti-6 atom % Si alloys. Scanning electron microscopy allowed us to evidence formation of compact and uniform polymer layers on the oxide surface. Photoelectrochemical and impedance measurements showed that photopolymerization allows one to grow PEDOT in its conducting state, while a strong cathodic polarization is necessary to bring the polymer in its p-type semiconducting state. Information on the optical and electrical properties of metal/oxide/polymer/electrolyte junctions proves that PEDOT has promising performance as an electrolyte…

Materials scienceFabricationElectrochemical fabricationInorganic chemistryImpedance measurementOxidePhysico-chemical characterizationPoly-3 4-ethylenedioxythiopheneElectrolyteElectrochemistrySettore ING-INF/01 - ElettronicaPhotoelectrochemistrychemistry.chemical_compoundPEDOT:PSSPhysical and Theoretical ChemistryConducting statechemistry.chemical_classificationPhotopolymerizationCathodic polarizationPolymerSilicon alloySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOptical and electrical propertieSettore ING-IND/23 - Chimica Fisica ApplicataGeneral EnergychemistryPolymerizationCavity magnetronLithium IntercalationTitanium alloyScanning electron microscopyThe Journal of Physical Chemistry C
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Microfluidic synthesis of micrometer-sized photoresponsive actuators based on liquid crystalline elastomers

2016

The fabrication of photoresponsive micrometer-sized liquid crystalline elastomer (LCE) particles has been described in this article for the first time. The preparation of the LCE particles using a microfluidic device by a continuous “on the fly” technique allows their fast processing with an irradiation time of less than 2 seconds. In order to accelerate the polymerization and to make the preparation of samples with thicknesses of several hundred microns possible, we modified a NIR-photoinitiation system by adding a bleaching agent. In addition to the photoinitiator, a side-chain liquid crystalline monomer containing an azo-group and a LC-crosslinker were used in the polymerization mixture.…

Materials scienceFabricationMicrofluidicsNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyElastomer01 natural sciences0104 chemical sciencesMicrometrechemistry.chemical_compoundMonomerchemistryChemical engineeringPolymerizationMaterials ChemistryArtificial muscleIrradiation0210 nano-technologyJournal of Materials Chemistry C
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Systematic Synthesis and Properties Evaluation of Dicationic Ionic Liquids, and a Glance Into a Potential New Field

2018

Dicationic ionic liquids (DILs), a subset of the ionic liquid (IL) family, have attracted growing interest in recent years, and the range of applications within which they are investigated is constantly expanding. However, data which allows structure to property correlation of a DIL is still limited, and thus selecting an appropriate salt to address a specific challenge can be problematic. In comparison to traditional ILs, DILs physico-chemical properties can be tuned by changing the length and type of spacer which connects the cationic heads as well as the type of cation. This in turn could give rise to symmetrical or asymmetrical DILs. In this work, a systematic study of a homogeneous cla…

Materials scienceField (physics)Salt (chemistry)02 engineering and technology010402 general chemistry01 natural sciencesDSClcsh:Chemistrychemistry.chemical_compounddicationic ionic liquids thermal analyses deep eutectic solvents TGA DSCComputational chemistryThermal stabilityCarboxylateOriginal ResearchEutectic systemdeep eutectic solventschemistry.chemical_classificationTGAthermal analysesHydrogen bondCationic polymerizationGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesdicationic ionic liquidsChemistrychemistrylcsh:QD1-999Ionic liquid0210 nano-technology
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Quantum-Chemical Insights into the Self-Assembly of Carbon-Based Supramolecular Complexes

2018

Understanding how molecular systems self-assemble to form well-organized superstructures governed by noncovalent interactions is essential in the field of supramolecular chemistry. In the nanoscience context, the self-assembly of different carbon-based nanoforms (fullerenes, carbon nanotubes and graphene) with, in general, electron-donor molecular systems, has received increasing attention as a means of generating potential candidates for technological applications. In these carbon-based systems, a deep characterization of the supramolecular organization is crucial to establish an intimate relation between supramolecular structure and functionality. Detailed structural information on the se…

Materials scienceFullereneNoncovalent interactionsSurface PropertiesSupramolecular chemistryPharmaceutical Sciencechemistry.chemical_elementNanotechnologyContext (language use)ReviewCarbon nanotube010402 general chemistry01 natural sciencesPolymerizationAnalytical Chemistrylaw.inventionquantum chemistrylcsh:QD241-441noncovalent interactionslcsh:Organic chemistrylawDrug DiscoveryNon-covalent interactionsQuímica FísicaPhysical and Theoretical Chemistrychemistry.chemical_classificationNanotubes Carbon010405 organic chemistryGrapheneOrganic Chemistrycarbon-based supramolecular assemblies0104 chemical sciencesCharacterization (materials science)Models ChemicalchemistryChemistry (miscellaneous)Quantum TheoryMolecular MedicineFullerenesCarbonQuantum chemistryAlgorithmsCarbon-based supramolecular assemblies
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Synthesis and Characterization of Isotactic Poly(1-hexene)/Branched Polyethylene Multiblock Copolymer via Chain Shuttling Polymerization Technique

2018

Understanding from the underlying mechanism of chain shuttling polymerization (CSP) is limited due to scarceness of successful reports and incompetence of traditional characterization techniques to distinguish blocky structures. Here, a simple synthesis approach for production of an isotactic poly(1-hexene)/branched polyethylene multiblock copolymer from a 1-hexene monomer is presented. Resulting copolymers can be easily characterized because of their solubility in most organic solvents. This novel blocky architecture is synthesized using ansa-ethylenebis(1-η5-indenyl)zirconium dichloride and α-diimine nickel(II) bromide catalysts. While the former participates in 1,2-enchainment of monomer…

Materials scienceGeneral Chemical Engineering02 engineering and technologyGeneral ChemistryPolyethylene010402 general chemistry021001 nanoscience & nanotechnologyChain shuttling polymerization01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationChain walkingTacticityPolymer chemistryCopolymerMolar mass distribution0210 nano-technologyIndustrial & Engineering Chemistry Research
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