Publications by authors named "R Leboda"

To control the properties of poly(dimethylsiloxane) (PDMS, Oxane 1000) as a bio-inert material, the characteristics of Oxane 1000 were compared for PDMS alone and interacting with silica gel Si-100 and nanosilica PS400. Low-temperature (1)H NMR spectroscopy, applied to static samples at 200-300 K, and differential scanning calorimetry (DSC) at 153-393 K were used to analyze the properties of PDMS and composites. The NMR study shows that liquid and solid-like fractions of PDMS co-exist over a broad temperature range.

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Detailed analysis of the interfacial behavior of water and weakly polar or nonpolar organics adsorbed alone or co-adsorbed onto activated carbons (AC) at different temperatures is a complex problem important for practical applications of adsorbents. Interaction of water, 1-decanol, and n-decane with AC possessing highly developed porosity (pore volume Vp≈1.4-2.

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The interfacial and temperature behavior of n-decane bound to weakly hydrated nanosilica A-400 (initial, heated, or compacted) or silica gel Si-60 was studied using low-temperature (1)H NMR spectroscopy applied to static samples that allowed us to observe signals only of mobile decane and unfrozen water molecules. For deeper insight into the phenomena studied, interactions of n-decane, 1-decanol, and water with a set of nanosilicas and silica gels were analyzed using DSC and thermoporometry. Both NMR and DSC results demonstrated that during heating of frozen samples at a heating rate of 5 K/min a portion of decane or decanol remained frozen at temperature higher than the freezing point of bulk liquid (Tf).

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The interfacial behavior of silicone oils Oxane 1000 and Oxane 5700 (polydimethylsiloxanes, PDMS) interacting with dried or hydrated (hydration h=0.005 or 0.1g/g) silica gels Si-60 and Si-100 or nanosilica A-400 was studied using low-temperature (1)H NMR spectroscopy over the 210-310 K range.

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Water, as a probe liquid bound in model systems (highly disperse hydroxyapatite - protein composites as a model of the main components of bones) and rat bone tissues healthy and affected by osteoporosis occurred due to experimental Alzheimer's disease (EAD), has been investigated using low-temperature (1)H NMR spectroscopy, NMR cryoporometry, TG/DTG/DTA, DSC, and TG and DSC thermoporometry. The textural characteristics of these intact systems cannot be studied using the standard adsorption methods, but the cryoporometry and thermoporometry methods give these characteristics. The (1)H NMR spectra of water bound in model and natural bone tissues include signals, which can be assigned to strongly associated (typical) water (SAW, chemical shift of proton resonance δ(H)=5-6 ppm) and weakly associated (atypical) water (WAW) at δ(H)=1-2 ppm.

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