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  • 1
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    MDPI - Multidisciplinary Digital Publishing Institute
    Publication Date: 2024-04-11
    Description: Nowadays, polymer self-assembly has become extremely attractive for both biological (drug delivery, tissue engineering, scaffolds) and non-biological (packaging, semiconductors) applications. In nature, a number of key biological processes are driven by polymer self-assembly, for instance protein folding. Impressive morphologies can be assembled from polymers thanks to a diverse range of interactions involved, e.g., electrostatics, hydrophobic, hots-guest interactions, etc. Both 2D and 3D tailor-made assemblies can be designed through modern powerful techniques and approaches such as the layer-by-layer and the Langmuir-Blodgett deposition, hard and soft templating. This Special Issue highlights contributions (research papers, short communications, review articles) that focus on recent developments in polymer self-assembly for both fundamental understanding the assembly phenomenon and real applications.
    Keywords: TA1-2040 ; T1-995 ; evaporative self-assembly ; encapsulation ; n/a ; microstructure ; solvent vapor annealing ; drug delivery ; polyhedral oligomeric silsesquioxane ; protein adsorption resistance ; photo-sensitive ; calcium carbonate ; fluorescence ; mucin ; polymerisation ; marine exopolysaccharide ; transglutaminases ; porous hydrogel ; adsorption ; aprotinin ; nanoparticle ; calcium alginate ; protamine ; nanocrystalline ; self-assembly ; morphological transformation ; cell culture ; block polymers ; stimuli-responsive polymer ; crosslinking ; mesoporous ; Ti6Al4V ; polymer ; flexible geometric confinement ; layer-by-layer ; surface modification ; co-synthesis ; nanolithography ; CaCO3 ; synthetic polypeptide ; air-liquid interface ; food industry ; stimuli-responsive polymers ; field-effect transistor ; Marangoni convection ; polymer scaffold ; collagen ; biomedicine ; thin films ; controlled release ; tension gradient ; monolayer ; thema EDItEUR::T Technology, Engineering, Agriculture, Industrial processes::TB Technology: general issues::TBX History of engineering and technology
    Language: English
    Format: application/octet-stream
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  • 2
    Publication Date: 2019-11-04
    Description: In order to describe and quantify the reactivity of silicate melts, the ionic notation provided by the Temkin formalism has been historically accepted, giving rise to the study of melt chemical equilibria in terms of completely dissociated ionic species. Indeed, ionic modelling of melts works properly as long as the true extension of the anionic matrix is known. This information may be attained in the framework of the Toop-Samis (1962a,b) model, through a parameterisation of the acid-base properties of the dissolved oxides. Moreover, by combining the polymeric model of Toop and Samis with the «group basicity» concept of Duffy and Ingram (1973, 1974a,b, 1976) the bulk optical basicity (Duffy and Ingram, 1971; Duffy, 1992) of molten silicates and glasses can be split into two distinct contributions, i.e. the basicity of the dissolved basic oxides and the basicity of the polymeric units. Application to practical cases, such as the assessment of the oxidation state of iron, require bridging of the energetic gap between the standard state of completely dissociated component (Temkin standard state) and the standard state of pure melt component at P and T of interest. On this basis it is possible to set up a preliminary model for iron speciation in both anhydrous and hydrous aluminosilicate melts. In the case of hydrous melts, I introduce both acidic and basic dissociation of the water component, requiring the combined occurrence of H+ cations, OH- free anions and, to a very minor extent, of T-OH groups. The amphoteric behaviour of water revealed by this study is therefore in line with the earlier prediction of Fraser (1975).
    Description: Published
    Description: JCR Journal
    Description: open
    Keywords: polymerisation ; basicity ; oxidationstate ; water speciation ; Temkin model ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.04. Thermodynamics
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Format: 1086720 bytes
    Format: application/pdf
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  • 3
    Publication Date: 2017-04-04
    Description: The effect of pressure on melt viscosity was investigated for five compositions along the join An(CaAl2Si2O8)–Di(CaMgSi2O6) and four alkali silicates containing lithium, sodium, and potassium in constant ratio of ∼ 1:1:1, but alkali-silica ratios are varying. The experiments were performed in an internally heated gas pressure vessel at pressures from 50 to 400 MPa in the viscosity range from 108 to 1011.5 Pa⋅s using parallel plate viscometry. The polymerized An composition shows a negative pressure dependence of viscosity while the other, more depolymerized compositions of the join An–Di have neutral to positive pressure coefficients. The alkali silicates display neutral to slightly positive pressure coefficients for melt viscosity. These findings in the high viscosity range of 108–1011 Pa⋅s, where pressure appears to be more efficient than in low viscous melts at high temperature, are consistent with previous results on the viscosity of polymerized to depolymerized melts in the system NaAlSi3O8–CaMgSi2O6 by Behrens and Schulze [ H. Behrens and F. Schulze, Am. Mineral. 88, 1351 (2003) ]. Thus we confirm that the sign of the pressure coefficient for viscosity is mainly related to the degree of melt polymerization in silicate and aluminosilicate melts.
    Description: DFG Grant n.°BE1720/9
    Description: Published
    Description: 044504-14
    Description: 2.3. TTC - Laboratori di chimica e fisica delle rocce
    Description: JCR Journal
    Description: open
    Keywords: viscosity ; polymerisation ; anorthite ; diopside ; 04. Solid Earth::04.08. Volcanology::04.08.99. General or miscellaneous
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimie 66 (1984), S. 645-650 
    ISSN: 0300-9084
    Keywords: derives mercures ; mercurated polymers ; mercury derivative ; polymeres mercures ; polymerisation ; polymerization ; ppUHgX or pUHgX ; ppUHgX ou pUHgX
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0300-9084
    Keywords: antimicrotubular drugs ; microtubules ; microtubules ; polymerisation ; polymerization ; produits anti-microtubulaires ; tubulin ; tubuline
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimie 66 (1984), S. 81-85 
    ISSN: 0300-9084
    Keywords: fibrin ; fibrin monomers ; fibrine ; fibrinogen ; fibrinogene ; magnetic orientation ; monomeres de fibrine ; orientation magnetique ; polymerisation ; polymerization
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 3 (1996), S. 255-264 
    ISSN: 1572-9028
    Keywords: plasmas ; catalysis ; polymerisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Heterogeneous and homogeneous non-equilibrium plasma chemistry offers a range of potential advantages compared to conventional thermal activation and synthesis methods. Some examples of how such low temperature electrical discharges can be effectively utilised for selective chemical reaction pathways are given. These include the fluorination of C-H bonds, the synthesis of polyozonides, selective ring opening polymerisation, and the conversion of alkali metal halides to nitrates using air.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-879X
    Keywords: beta ; polymerisation ; polystyrene ; styrene ; USY ; zeolites
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The homopolymerisation of styrene is studied in the presence of Y, USY and beta zeolites. High molecular weight polymers, in the range 0.7 × 106–1 × 106, are obtained in good yields. The activity of zeolite beta is only slightly increased by calcination of the as-synthesised material, pointing to an important role of the zeolite outer surface. The influence of the catalyst acidity upon the polymer molecular weight is evaluated by the use of dealuminated zeolites.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 7 (1996), S. 203-209 
    ISSN: 1573-4846
    Keywords: gel silica glass ; thermal analysis ; glass transition temperature ; polymerisation ; poly-methylmethacrylate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal analysis of poly-methylmethacrylate (PMMA) impregnated porous gel silica glasses confirms that the PMMA chains form hydrogen bonds with the pore surface silanol groups. The adopted conditions for the insitu polymerisation result in about 4% of residual monomers trapped in the polymer, most of them in the amorphous structure. The polymer and monomer mixture takes up the whole of the free pore volume. Most of the residual monomer polymerises during the DSC scans above the glass transition temperature providing an excellent probe for the weak glass transition. Polymerisation in the gel silica glass medium affects the glass transition temperature, the length of polymer chains, and the degree of polymerisation.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 9 (1999), S. 235-250 
    ISSN: 1572-9028
    Keywords: Ziegler–Natta ; density functional theory ; adsorption ; polymerisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Total energy pseudopotential calculations have been used to examine the adsorption of TiCl4 at both the 110 and 100 surfaces of magnesium chloride. Titanium(IV) chloride is found to bind most strongly on the 100 surface resulting in the formation of a complex with approximately trigonal bipyramidal coordination of titanium, which will dissociate to form TiCl 3 + and Cl− with an energy of 127.7 kJ mol−1. Cluster calculations indicate that this site only weakly binds ethene, but does catalyse the formation of C–C bonds with an activation energy consistent with experimental estimates.
    Type of Medium: Electronic Resource
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