Spin probe study of semi‐interpenetrating polymer networks based on polyurethane and polymethacrylate functional prepolymers

The motional transition and heterogeneity of semi‐interpenetrating networks (SIPNs) based on polyurethane (PU) with carboxylic groups and methacrylic copolymer (PM) with tertiary amine groups were studied by the electron spin resonance (ESR) spin probe method. The concentration of functional groups in both prepolymers varied from 0 to 0.45 mmol g^?1. Spin‐probed SIPNs show that the temperature‐dependent spectra are sensitive to polymer interactions imposed by functional groups. These interactions determine the free volume distribution in the matrix and temperature at which motional transition takes place. The fraction of free volume increases with functional group concentration and reaches its maximum at 0.25 mmol g^?1. Further increases in the functional group concentration reduce the free volume. The results of the networks with strong interactions are discussed in terms of the interference of the plasticizing effect of the PU component and the formation of possible cluster cross‐links, which restricts segmental motions. Copyright © 2003 Society of Chemical Industry     

Motional heterogeneity of segmented polyurethane-polymethacrylate mixtures: an influence of functional groups concentration

The motional heterogeneity in the polymer mixtures of segmented polyether polyurethane (PU) with carboxylic groups and methacrylic copolymer (PM) with tertiary amine groups was studied by the electron spin resonance (ESR)—spin probe and spin label methods. Pure polymer components containing varying amounts of functional groups and their 1:1 mass ratio mixtures have been analysed. The results of motional heterogeneity and polymer interaction were complemented with the glass transition temperatures, structural and morphological characteristics. Spin probed PU/PM mixtures indicate that the probe motion and the phase separation deduced from the temperature-dependent ESR spectra are sensitive to a free volume determined by the polymer-polymer interactions. The interaction between the two components in PU/PM mixture with the highest functional groups concentration disorganizes hard segment domains with spherulitic character at the microscopic level as compared with the ordered hard phase in the corresponding pure PU sample. The influence of PU hard and soft segments on the motional dynamics of PM chains is analysed from the ESR spectra of spin labelled PM chains in the mixtures with unlabelled PU components. The fractional amount of the PM fast motion depends on the temperature and concentration of functional groups.     

Main chain and segmental dynamics of semi interpenetrating polymer networks based on polyisoprene and poly(methyl methacrylate)

Main chain and segmental dynamics of polyisoprene (PI) and poly(methyl methacrylate) (PMMA) chains in semi IPNs were systematically studied over a wide range of temperatures (above and below T_g of both polymers) as a function of composition, crosslink density, and molecular weight. The immiscible polymers retained most of its characteristic molecular motion; however, the semi IPN synthesis resulted in dramatic changes in the motional behavior of both polymers due to the molecular level interpenetration between two polymer chains. ESR spin probe method was found to be sensitive to the concentration changes of PMMA in semi IPNs. Low temperature spectra showed the characteristics of rigid limit spectra, and in the range of 293-373 K, complex spectra were obtained with the slow component mostly arising out of the PMMA rich regions and fast component from the PI phase. We found that the rigid PMMA chains closely interpenetrated into the highly mobile PI network imparts motional restriction in nearby PI chains, and the highly mobile PI chains induce some degree of flexibility in highly rigid PMMA chains. Molecular level interchain mixing was found to be more efficient at a PMMA concentration of 35 wt.%. Moreover, the strong interphase formed in the above mentioned semi IPN contributed to the large slow component in the ESR spectra at higher temperature. The shape of the spectra along with the data obtained from the simulations of spectra was correlated to the morphology of the semi IPNs. The correlation time measurement detected the motional region associated with the glass transition of PI and PMMA, and these regions were found to follow the same pattern of shifts in α-relaxation of PI and PMMA observed in DMA analysis. Activation energies associated with the T_g regions were also calculated. T_50G was found to correlate with the T_g of PMMA, and the volume of polymer segments undergoing glass transitional motion was calculated to be 1.7 nm³. C-13 T_1ρ measurements of PMMA carbons indicate that the molecular level interactions were strong in semi IPN irrespective of the immiscible nature of polymers. The motional characteristics of H atoms attached to carbon atoms in both polymers were analyzed using 2D WISE NMR. Main relaxations of both components shifted inward, and both SEM and TEM analysis showed the development of a nanometer - sized morphology in the case of highly crosslinked semi IPN.     

Temperature dependence of molecular motions in the polyurethane-based membranes studied with paramagnetic spin probe

This third paper in this series regarding structure and dynamics of the polyurethane-based membranes studied with TEMPO spin probe presents the results of the ESR measurements performed to characterise mobility of segments in the permeable regions of the membranes. The variations of the spin probe motions with temperature have been analysed for the series of polyurethanes (PU) differing in molecular structure and compared with the results of the DSC studies. Along with T_50 G, the other temperatures, T_n, T_i, T_τ, at which the significant change in dynamics occurs have been determined and correlated with the length of the PU soft and hard segments, and then discussed with regard to the respective relationships of T_g. The results have demonstrated the sensitivity of the ESR method to the segmental motions, which have not been detected by the DSC technique. From the DSC and ESR data the size of the motional chain segment in various PUs has been estimated, which has been found to follow the trend that polymers with higher T_g have bulkier segments. Two unusual observations have been made, concerning the deviation from the Arrhenius relation at high temperature for some PUs, and the increased mobility of the TEMPO molecules in some poly(urethane-urea)s after their thermal treatment. These results have been interpreted so far either in terms of the possible translational diffusion of the TEMPO molecules for those PUs showing lesser amount of the hard segments, or in terms of the increased free volume resulting from the temperature induced structural changes within the permeable regions of poly(urethane-urea)s.     

The study of poly(styrene-co-p-(hexafluoro-2-hydroxylisopropyl)-α-methyl-styrene)/poly(propylene carbonate) blends by ESR spin probe and Raman

Different hydroxyl content poly(styrene-co-p-(hexafluoro-2-hydroxyisopropyl)-α-methylstyene) [PS(OH)] copolymers were synthesized and blends [noted for PP-X] with poly(propylene carbonate) [PPC] were prepared by casting from chloroform solution. The miscibility, micro heterogeneity and hydrogen bonding interaction of the component polymers were investigated by Differential Scanning Calorimetry (DSC), Electron Spin Resonance (ESR) spin probe method and Micro Raman spectroscopy. DSC results showed that the PP-2, PP-5, PP-8, PP-12 blends exhibited two distinct T_gs, indicating immiscibility, while the PP-20 and PP-27 blends were miscible with the existence of a single T_g. ESR results indicated that the probe molecule: Tempo couldn't give clear micro phase separation or miscibility information and thus was not sensitive to the investigated polymer blends system. On the contrary for all the blends spin probed with the probe molecules: Tempol and Tamine, two spectral components with different rates of motion: ‘fast’ and ‘slow’ motion were observed in different temperature range, which indicated the existence of micro heterogeneity on the molecular level; the more mobile PPC-rich micro phase and the more rigid PS(OH) rich micro phase. In addition, the scale of miscibility was progressively enhanced due to the increasing hydrogen bonding interaction between the hydroxyl in PS(OH) and the oxygen atoms in PPC. Meanwhile it was found that the degree of the probe molecule rotation detectable in the ESR spectrum was dependent on the polymer matrix rigidity and the strength of the hydrogen bonding between the probe molecule and the polymer matrix. Micro Raman substantiated the existence of the PS(OH)-rich micro phase and the PPC-rich micro phase. The hydrogen bonding strength between PS(OH) and PPC and the mixing level of the component polymers were increased gradually with the increase of hydroxyl content in the PS(OH) copolymer.     

Structure–property relationship of polyethylene glycol‐based PU/PAN semi‐interpenetrating polymer networks

Polyethylene glycol‐400 (PEG) based polyurethane (PU) and polyacrylonitrile (PAN) semi‐interpenetrating polymer networks (SIPNs) (PU/PAN; 90/10, 70/30, 60/40, and 50/50) have been prepared by sequential polymerization method. The prepared SIPNs have been characterized by physicomechanical properties. The microcrystalline parameters such as crystal size (〈N〉), lattice disorder (g), surface (D_s) and volume (D_v) weighted crystal size of SIPNs have been estimated using wide angle X‐ray scattering studies, and quantification of the polymer network has been carried out on the basis of these parameters. The microstructural parameters have been established using Exponential, Lognormal, and Reinhold asymmetric column length distribution functions and the results are compiled. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 177–187, 2006     

Permeable domains of segmented polyurethanes studied with paramagnetic spin probe

Studies on the permeable regions of the dense polyurethane-based membranes were performed by electron spin resonance spectroscopy (ESR) using TEMPO spin probe incorporated into the membrane via diffusion from the vapour phase. The ESR spectra were measured as a function of temperature and microwave power for polyurethanes (PU) varying in the molecular structure and morphology. It was found that the TEMPO spin probe exhibited anisotropic rotation whose anisotropy increased as temperature decreased and was more pronounced for PU with shorter soft segments. The simplified method was used to obtain apparent correlation time τ_c enabling the comparison of the polyurethanes studied. This approach was based on the Arrhenius relation of τ_c vs. 1/T determined from motionally narrowed ESR spectra and on the assumption that this behaviour prevails over a broader temperature range at temperatures generally greater than T_g of a given polymer.     

The study of poly(styrene‐co‐p‐(hexafluoro‐2‐hydroxylisopropyl)‐α‐methylstyrene)/poly(ethylene oxide) blends

Different hydroxyl content poly(styrene‐co‐p‐(hexafluoro‐2‐hydroxylisopropyl)‐α‐methylstyene) [PS(OH)‐X] copolymers were synthesized and blends with 2,2,6,6‐tetramrthyl‐piperdine‐1‐oxyl end spin‐labeled PEO [SLPEO] were prepared. The miscibility behavior of all the blends was predicted by comparing the critical miscible polymer–polymer interaction parameter (χ_crit) with the polymer–polymer interaction parameter (χ). The micro heterogeneity, chain motion, and hydrogen bonding interaction of the blends were investigated by the ESR spin label method. Two spectral components with different rates of motion were observed in the ESR composite spectra of all the blends, indicating the existence of microheterogeneity at the molecular level. According to the variations of ESR spectral parameters T_a, T_d, ΔT, T_50G and τ_c, with the increasing hydroxyl content in blends, it was shown that the extent of miscibility was progressively enhanced due to the controllable hydrogen bonding interaction between the hydroxyl in PS(OH) and the ether oxygen in PEO. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2312–2317, 2004     

Motional heterogeneity of polystyrene-block-polybutadiene: a spin probe study

Polystyrene-block-polybutadiene copolymers (SB) with 0.5 mass fraction of styrene were studied by electron spin resonance (ESR) of nitroxide spin probes. The influence of the block length ( and ) and the solvation power of casting solvents on the motional dynamics of spin probe were measured over a wide temperature range. Two nitroxide radicals as spin probes were selected: 2,2,6,6-tetramethyl-4-hydroxypiperidine-1-oxyl benzoate (BzONO) and 2,2,6,6-tetramethyl-4-hydroxypiperidine-1-oxyl (Tempol). Irrespective of the spin probe used two ESR spectral components differing in their motional properties above the phase transition of polybutadiene blocks (PB) were observed. The fast component was assigned to spin probes located in polybutadiene-rich domains and the slow component to spin probes in polystyrene-rich domains. The range of two spectral components and the phase transition of the slow ESR component, T_5mT, depend on the block length. The influence of the interphase and accumulation of free volume in the interphase on the Tempol probe motion was investigated by changing copolymer morphology in the films casted from selective and nonselective solvents. The analysis of the motional heterogeneity from the ratio of the fast and slow motional component presents evidence that in the selective solvent for polystyrene (PS) blocks (2-butanone) the most irregular structure with a large interphase is formed. The difference in fast motion of spin probes indicates that the motional dynamic is related to the change of domain structure.     

Morphology and mechanical properties of semi-interpenetrating polymer networks from polyurethane and benzyl konjac glucomannan

A series of semi-interpenetrating polymer network (semi-IPN) films coded as UB from castor oil-based polyurethane (PU) and benzyl konjac glucomannan (B-KGM) were prepared, and they have good or certain miscibility over entire composition range. Morphology, miscibility and properties of the UB films were investigated by using scanning electron microscopy (SEM), differential scanning calorimetry, dynamic mechanical analysis, ultraviolet spectrometer, wide-angle X-ray diffraction and tensile test. The results indicated that the UB films exhibited good miscibility when B-KGM content was lower than 15 wt%, resulting in relatively high light transmittance, breaking elongation and density. With an increase of the B-KGM content from 20 to 80 wt%, a certain degree of phase separation between PU and B-KGM occurred in the UB films. The tensile strength of the films UB increased from 7 to 45 MPa with an increase of B-KGM content from 0 to 80 wt%. By extracting the B-KGM with N, N-dimethylformamide from the semi-IPN, the morphology and phase domain size of the UB films were clearly observed by SEM. A continuous phase and dual-continuous phase model describing the semi-IPN were proposed to illustrate the morphology and its transition.     

Tetracycline release from bioerodible hydrogels based on semiinterpenetrating polymer networks composed of poly(ε-caprolactone) and poly(ethylene glycol) macromer in vitro

Poly(ethylene glycol) (PEG) macromers terminated with acrylate groups and semiinter-penetrating polymer networks (SIPNs) composed of poly(ε-caprolactone) (PCL) and PEG macromer were synthesized and characterized with the aim of obtaining a bioerodible hydrogel that could be used to release tetracycline HCl for local antibiotic therapy administered peroperatively. Polymerization of PEG macromer resulted in the formation of crosslinked gels due to the multifunctionality of macromer. Noncrosslinked PCL chains were interpenetrated into the crosslinked three-dimensional networks of PEG. Glass transition temperature (T_g) and melting temperature (T_m) of PCL in the SIPNs were inner shifted, indicating interpenetration of PCL and PEG chains. It was found that water content increased with increasing PEG weight fraction due to the hydrophilicity of PEG. Drug release can be controlled by weight fraction of PEG in the PCL/PEG SIPNs, concentration of PEG macromer in the SIPNs preparation, and the nature of PEG. © 1996 John Wiley & Sons, Inc.     

A polyblend electrolyte (PVP/PEG+KI+I2) for dye-sensitized nanocrystalline TiO2 solar cells

A novel polyblend electrolyte consisting of KI and I₂ dissolved in a blending polymer of polyvinyl pyrrolidone (PVP) and polyethylene glycol (PEG) was prepared. The formation of ⁻I₃ in the polymer electrolyte was confirmed by X-ray photoelectron spectroscopy (XPS) characterization. Due to the coordinating and plasticizing effect by PVP, the ionic conductivity of the polyblend electrolyte is enhanced. The highest ionic conductivity of 1.85 mS cm⁻¹ for the polyblend electrolyte was achieved by optimizing the compositions as 40 wt.% PVP + 60 wt.% PEG + 0.05 mmol g⁻¹ I₂ + 0.10 mmol g⁻¹ KI. Based on the polyblend electrolyte, a DSSC with fill factor of 0.59, short-circuit density of 9.77 mA cm⁻², open-circuit voltage of 698 mV and light-to-electricity conversion efficiency of 4.01% was obtained under AM 1.5 irradiation (100 mW cm⁻²).     

Electron spin resonance of VO radical-ion in sub- and supercritical water

Electron spin resonance (ESR) spectra of VO²⁺ radical-ions in sub- and supercritical water are observed. Upon increasing the temperature from 20 to 100 °C, the fine structure line widths in the ESR spectra of the vanadyl ion are observed to be reduced that is associated with the effective averaging of the g-factor anisotropy and the hyperfine interaction. With further increasing the temperature, the spectrum components of the hyperfine structure are broadened significantly resulting in the unresolved low-intensity line in supercritical water with ΔH_pp ∼ 300 G. The data obtained allow behavior peculiarities of the paramagnetic VO²⁺ ions in sub- and supercritical water including rotational dynamics and spin exchange between the radicals to be elucidated. The registration of the unresolved low-intensity line in supercritical conditions points to an increase in the local ion concentration in the system that can be an initial stage for the formation of vanadium-based particles in supercritical conditions. The study demonstrates that ESR is the powerful tool to investigate properties of sub- and supercritical water in situ.     

Recent studies on interpenetrating polymer networks

Recent investigations on interpenetrating polymer networks (IPNs) have included two component IPNs from polyurethanes and poly(methacrylates) and two component IPNs from polyurethanes and epoxies. All the IPNs were prepared by the simultaneous polymerization technique (SIN-IPNs). Two types of IPNs, polyurethane-poly(methyl methacrylate) (PU/PMMA) and polyurethane-poly(methyl methacrylate-methacrylic acid) (PU/PMMA-MAA) were prepared. Improved phase miscibility and decreasing extent of phase separation was observed in both types of IPNs with increasing the NCO/OH ratio, decreasing molecular weight of the polyol in the PU and introduction of charge groups. A comparison was made between full-IPNs, pseudo-IPNs, graft copolymers and related homopolymers from polyurethanes and epoxies. Increased compatibility in full-IPNs and graft copolymers was observed by means of DSC, SEM and was also further substantiated by a shift toward single T_gs as determined by dynamic mechanical spectroscopy. The introduction of opposite charge groups in two-component IPNs from polyurethanes and epoxies led to improved compatibility (no phase separation) and enhanced mechanical properties.     

Study of miscibility enhancement in poly(styrene‐co‐4‐vinylphenol)/poly(ethylene oxide) blends by the spin labelling method

The electron spin resonance (ESR) spectra of end‐group spin labelled poly(ethylene oxide) (SLPEO) using 2,2,6,6‐tetramethyl‐piperdine‐1‐oxyl nitroxide and its blends with poly(styrene‐co‐4‐vinylphenol) (STVPhs) of different hydroxyl contents were recorded over a wide temperature range. For a blend of SLPEO and pure polystyrene (PS), the ESR spectrum was composed of a single motion component, indicating that PS was immiscible with PEO. For blends composed of SLPEO and different‐hydroxyl‐content STVPhs, two spectral components with different motion rates were observed over a certain temperature range. The difference between the motion rates should be attributed to micro‐heterogeneity in the blends, with the faster rate corresponding to a nitroxide radical motion trapped in the PEO‐rich domain and the slower rate corresponding to a nitroxide radical motion trapped in the STVPh‐rich domain. Variations in the values of a number of the ESR parameters (T_a, T_d and T_50G) and the apparent activation energy (E_a) with hydroxyl content in the blends indicated that the miscibility of the blends increased with increasing hydrogen‐bonding density due to specific interactions between the hydroxyl groups in STVPh and the ether oxygens in PEO. Copyright © 2004 Society of Chemical Industry     

Preparation and properties of starch thermoplastics modified with waterborne polyurethane from renewable resources

A waterborne polyurethane (PU) aqueous dispersion was synthesized from castor oil, and blended with thermoplastic starch (TPS) to obtain a novel biodegradable plastic with improved physical properties. The effect of PU content on the morphology, miscibility and physical properties of the resulting blends was well investigated by scanning electron microscopy, differential scanning calorimetry, dynamic mechanical thermal analysis and measurements of mechanical properties and water sensitivity. The research results show that the blends exhibit a higher miscibility when PU content is lower than 15 wt% due to the hydrogen bonding interaction between urethane groups and hydroxyl groups on starch, whereas obviously phase separation occurs in the blends with more than 15 wt% PU. Incorporating PU of 4-20 wt% in TPS results in the blends with improved Young's modulus (40-75 MPa), tensile strength (3.4-5.1 MPa), elongation at break (116-176%). Further, PU also plays an important role in improving the surface- and bulk-hydrophobicity and water resistance of the resulting blends.     

Hydrophilic polymer supports grafted by poly(ethylene glycol) derivatives via atom transfer radical polymerization

In this study, a newly structured hydrophilic polymer supports are prepared by the chemical modification (grafting) of the polystyrene-based preformed beads via atom transfer radical polymerization (ATRP) employing the CuBr/PMDETA catalyst system. Hydrophilic monomers including N,N-dimethylacrylamide (DMA) and poly(ethylene glycol) (PEG) macromonomers were grafted onto Merrifield type resin. Based on optical microscopic data, the particle sizes of the resins were increased in the order of 10 μm after the polymerization. This increment indicated that monomers are grafted not only to the particle surface but also to within a polymer matrix. These resins demonstrate well-swellability in polar solvent, and they enable high functional loadings up to 0.7-1.8 mmol g⁻¹. The high loading capacity in polar solvents and favorable mechanical properties of resins render them to have great potential applications in peptide and oligonucletide syntheses.     

Synthesis of a poly(vinylcatechol-co-divinylbenzene) resin and accessibility to catechol units

Poly(vinylcatechol-co-divinylbenzene) resins have been prepared by suspension copolymerization of 3,4-dimethoxystyrene (DMS) with divinylbenzene (DVB) using toluene as the porogen and followed by deprotection of the catechol functions. The ratio of DMS versus DVB was modified and led to a maximum catechol content (determined by elemental analysis) varying from 0.82 to 3.16 mmol g⁻¹. Large surface areas were found for copolymers prepared with a divinylbenzene content larger than 35% v/v: from 464 to 658 m² g⁻¹. Accessibility (determined by back titration of the hydroxyl groups) was improved by prior contact with ethanol but remained inferior to 20%. This can be the result of the morphology of the resin beads and of the bottle-shape form of the pores, or/and of the embedding of the catechol units inside the polymer network. The sorption capacities were determined for Cu(II) and Cd(II) and reached 101.5 and 81.0 μmol g⁻¹ for copper and cadmium, respectively. Moreover, a significant variation of coloration has been observed upon complexation of copper by the resins.     

Polyurethane–polystyrene interpenetrating polymer networks synthesized at low temperature: Effect of crosslinking level

Interpenetrating polymer networks (IPNs) of polyurethane (PU)–polystyrene (PS) containing 50 wt % PU were synthesized at low temperature with varying crosslink density of each component. PU was polymerized first, followed by the photopolymerization of PS at low temperature (0 and 40°C). The theoretical molecular weight between crosslink (M?_c) of PU ranged from 8200 to 2050, and the M?_c of PS varied from linear to 2000. The degree of mixing of the components in these IPNs was investigated using dynamic mechanical analysis, electron microscopy, and density measurement. The degree of mixing increased with decreasing M?_c and/or synthesis temperature. The crosslink density variation at low synthesis temperature is more effective in enhancing the miscibility of IPN than at high synthesis temperature, because both the temperature and crosslink density can affect the polymer chain mobility during the synthesis. The variation of PU network crosslink density shows the better effect in increasing the miscibility of IPN than that of the PS network. The morphology and the density behavior agree well with the dynamic mechanical result.     

Synthesis and characterization of polyurethane–chitosan interpenetrating polymer networks

A polyurethane–chitosan (PU–CH) coating was synthesized from castor-oil-based PU prepolymer and highly deacetylated and depolymerized chitosan. The films cast with the coating were used for the characterization. X-ray photoelectron spectroscopy, a surface-sensitive technique, indicated the chemical bonding between the chitosan and PU prepolymer as well as the enrichment of chitosan on the surface of the film PU–CH. Electron spin resonance (ESR) spectroscopy using the nitroxyl radical 4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl (4-hydroxy-TEMPO) as a reporter group was used to study the chain mobility in the film PU–CH. It was observed that T_50G of the probe and the first glass transition temperature (T_g1) of the film PU–CH were 10 and 18°C higher than those in the PU film, respectively, and the activation energy (27.0 kJ mol⁻¹) of tumbling for the probe covalently bonded with PU–CH was 12.8 kJ mol⁻¹ higher than that of the probe with the film PU. It suggests that the molecular motion in the PU–CH was restricted by grafted and crosslinked interpenetrating polymer networks (IPNs). The results of the differential thermal analysis and thermogravimetric analysis proved that the thermostability of the film PU–CH was significantly higher than that of the film PU, and the T_g1 value is in good agreement with that calculated from ESR. It could be concluded that the IPNs resulted from the chitosan grafting and crosslinking with PU exist in the film PU–CH. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1321–1329, 1998