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showing 10 items of 2078 documents

Stratification of polymer mixtures in drying droplets: Hydrodynamics and diffusion

2020

We study the evaporation-induced stratification of a mixture of short and long polymer chains in a drying droplet using molecular simulations. We systematically investigate the effects of hydrodynamic interactions (HI) on this process by comparing hybrid simulations accounting for HI between polymers through the multiparticle collision dynamics technique with free-draining Langevin dynamics simulations neglecting the same. We find that the dried supraparticle morphologies are homogeneous when HI are included but are stratified in core--shell structures (with the short polymers forming the shell) when HI are neglected. The simulation methodology unambiguously attributes this difference to th…

chemistry.chemical_classificationMaterials science010304 chemical physicsFOS: Physical sciencesGeneral Physics and AstronomyThermodynamicsStratification (water)PolymerCondensed Matter - Soft Condensed Matter010402 general chemistry01 natural sciences0104 chemical sciencesCondensed Matter::Soft Condensed MatterSolventCollision dynamicschemistryHomogeneous0103 physical sciencesSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryLangevin dynamicsBackflowThe Journal of Chemical Physics
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Influence of the position of two dehydro-amino acids residues in the oligopeptide sequence on the binding ability towards Cu(II) ions

2005

Abstract Studies on the binding ability of bis-dehydro-hexa- and pentapeptides have shown that the hexapeptides bind Cu+2 with similar efficacy as pentapeptides. The increase of distance between two dehydro-amino acid residues in the peptide backbone has no impact on the efficacy in metal ion binding. The type of isomeration [(Z) or (E)] has an influence on the coordination of the metal ion only to the first amide nitrogen.

chemistry.chemical_classificationOligopeptideStereochemistrySequence (biology)IonAmino acidInorganic ChemistryMetalchemistry.chemical_compoundBinding abilityCopper(II)Peptide backbonechemistryAmidevisual_artMaterials Chemistryvisual_art.visual_art_mediumdehydro-peptidesOrganic chemistryPhysical and Theoretical ChemistrycomplexPolyhedron
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Structure of bottle brush polymers on surfaces: weak versus strong adsorption.

2011

Large-scale Monte Carlo simulations are presented for a coarse-grained model of cylindrical molecular brushes adsorbed on a flat structureless substrate, varying both the chain length N of the side chains and the backbone chain length N(b). For the case of good solvent conditions, both the cases of weak adsorption (only 10 to 15% of the monomers being bound to the surface) and strong adsorption (~40% of the monomers being bound to the surface, forcing the bottle brush into an almost 2D conformation) are studied. We focus on the scaling of the total linear dimensions of the cylindrical brush with both chain lengths N and N(b), demonstrating a crossover from rod-like behavior (for not very la…

chemistry.chemical_classificationPersistence lengthQuantitative Biology::BiomoleculesChemistryMonte Carlo methodBrushBackbone chainPolymerSurfaces Coatings and Filmslaw.inventionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAdsorptionChemical physicslawPolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryScalingThe journal of physical chemistry. B
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Conformational studies of bottle-brush polymers absorbed on a flat solid surface.

2010

The adsorption of a bottle-brush polymer end-grafted with one chain end of its backbone to a flat substrate surface is studied by Monte Carlo simulation of a coarse-grained model, that previously has been characterized in the bulk, assuming a dilute solution under good solvent conditions. Applying the bond fluctuation model on the simple cubic lattice, we vary the backbone chain length $N_b$ from $N_b=67$ to $N_b = 259$ effective monomeric units, the side chain length $N$ from N=6 to N=48, and the grafting density $\sigma=1$, i.e., parameters that correspond well to the experimentally accessible range. When the adsorption energy strength $\epsilon$ is varied, we find that the adsorption tra…

chemistry.chemical_classificationRange (particle radiation)Quantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodGeneral Physics and AstronomyBackbone chainThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterGyrationCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerAdsorptionchemistrySide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryThe Journal of chemical physics
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Microstructure of a Discotic Polymer as Revealed by Electron Diffraction and High-Resolution Imaging

1989

chemistry.chemical_classificationReflection high-energy electron diffractionMaterials scienceAnalytical chemistryGeneral MedicineGeneral ChemistryPolymerMicrostructureCatalysisCrystallographychemistryElectron diffractionHigh resolution imagingElectron backscatter diffractionAngewandte Chemie International Edition in English
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Computational Analysis of n→π* Back-Bonding in Metallylene–Isocyanide Complexes R2MCNR′ (M = Si, Ge, Sn; R = tBu, Ph; R′ = Me, tBu, Ph)

2013

A detailed computational investigation of orbital interactions in metal–carbon bonds of metallylene–isocyanide adducts of the type R2MCNR′ (M = Si, Ge, Sn; R, R′ = alkyl, aryl) was performed using density functional theory and different methods based on energy decomposition analysis. Similar analyses have not been carried out before for metal complexes of isocyanides, even though the related carbonyl complexes have been under intense investigations throughout the years. The results of our work reveal that the relative importance of π-type back-bonding interactions in these systems increases in the sequence Sn < Ge ≪ Si, and in contrast to some earlier assumptions, the π-component cannot be …

chemistry.chemical_classificationStereochemistryLigandIsocyanideArylOrganic ChemistryAdductInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artvisual_art.visual_art_mediumDensity functional theoryPhysical and Theoretical Chemistryta116AlkylPi backbondingOrganometallics
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1979

The thermal degradation behavior of head-to-head (H-H) and head-to-tail (H-T) polystyrenes and poly(vinylcyclohexane)s has been investigated by direct pyrolysis in a mass spectrometer. Both H-H and H-T isomers show only small differences in their initial temperatures of decomposition but remarkably different degradation processes. Whereas H-T polystyrene decomposes in accordance with earlier investigations mainly by a radicalic depolymerization into the monomer and yields only a small amount of dimer and trimer, the H-H polystyrene shows no unzipping and only a statistic degradation into oligomeric styrenes. The formation of stilbene is a diagnostic reaction of H-H polystyrene. The pyrolysi…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceMonomerchemistryDepolymerizationDimerPolymer chemistryBackbone chainTrimerPolymerPolystyrenePyrolysisDie Makromolekulare Chemie
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Effective conjugation in conjugated polymers with strongly twisted backbones: A case study on fluorinated MEHPPV

2016

Conjugated polymers with strongly twisted backbones, such as MEHPPV with fluorinated vinylene units (F-MEHPPV), demand a redefinition of the all-important ‘effective conjugation length’ ECL, which we extract here by a facile graphical method. In MEHPPV (being essentially planar), the ECL coincides with the ‘maximum conducive chain length’ MCC and extends over about n ≈ 9 repetition units (RU). In F-MEHPPV, the MCC is similarly long with n ≈ 8, but the ECL localizes on just one RU. The strong twist in F-MEHPPV persists in the excited state, broadening the emission spectrum and quenching the fluorescence with reduced radiative and enhanced non-radiative rates.

chemistry.chemical_classificationfluorinated MEHPPVMaterials scienceQuenching (fluorescence)twisted backbones02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesChain lengthPlanarchemistryExcited stateEffective conjugationMaterials ChemistryEmission spectrum0210 nano-technology
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Prawo dziecka do wiadomości o swoim pochodzeniu

2017

childfamilyfamily backgroundchildren'sthe right to information
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Renewable Energy Technologies for Economic Development

2020

Indonesian villages are facing dangerous condition. Every year, young people are deserting the villages. To overcome this problem, Tangsi Jaya hamlet, West Java, has been provided with 18 kW micro-hydro to supply electricity both to the community and to Small Processing Center for ground coffee production. Results of cash flow analysis for ground coffee in Tangsi Jaya hamlet, with total investment of IDR 110 750 000 and discount rate of 18 % for 5 yr. Banyumeneng I hamlet, Yogyakarta with an investment cost IDR 95 000 000 and production cost of IDR 34 195 000 yr–1 and the interest rate of 14 % yr–1, the payback period was estimated to be 3 yr with ROI of 40 %. PEST analysics indicate that t…

clean energyzero wasteEconomic growthPayback periodmedia_common.quotation_subject0211 other engineering and technologiesZero wasteTariff02 engineering and technology010501 environmental sciences01 natural sciencesCash flow analysisincrease economic sector in rural areawaste utilization021108 energylcsh:Environmental sciences0105 earth and related environmental sciencesmedia_commonlcsh:GE1-350business.industryInterest rateRenewable energysmall processing centerElectricityRural areabusinessE3S Web of Conferences
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