Relaxation NMR as a tool to study the dispersion and formulation behavior of nanostructured carbon materials.

Solvent relaxation NMR has been used to estimate the surface areas and wettability of various types of nanostructured carbon materials in a range of solvents including water, ethanol, and tetrahydrofuran. We illustrate the application of the technique through several short case studies using samples including nanocarbon blacks, graphene oxide, nanographites, and porous graphenes. The technique is shown to give a good measure of surface area, correlating well with conventional surface area estimates obtained by nitrogen adsorption, transmission electron microscopy, or light scattering for the non-porous samples. NMR relaxation has advantages in terms of speed of analysis and being able to use concentrated, wet, and opaque samples. For samples that are porous, two distinct surface areas can be estimated assuming the two environments ('inner' and 'outer') have the same surface chemistry, and that there is a slow exchange of solvent molecules between them. Furthermore, we show that differences in wettability and dispersability between samples dispersed in water, ethanol, and cyclopentanone can be observed, along with changes to the surface chemistry of the interface. Copyright © 2015 John Wiley & Sons, Ltd.

Interpolymer complexation: comparisons of bulk and interfacial structures.

The interactions between the strong polyelectrolyte sodium poly(styrenesulfonate), NaPSS, and the neutral polymer poly(vinylpyrrolidone), PVP, were investigated in bulk and at the silica/solution interface using a combination of diffusion nuclear magnetic resonance spectroscopy (NMR), small-angle neutron scattering (SANS), solvent relaxation NMR, and ellipsometry. We show for the first time that complex formation occurs between NaPSS and PVP in solution; the complexes formed were shown not to be influenced by pH variation, whereas increasing the ionic strength increases the complexation of NaPSS but does not influence the PVP directly. The complexes formed contained a large proportion of NaPSS. Study of these interactions at the silica interface demonstrated that complexes also form at the nanoparticle interface where PVP is added in the system prior to NaPSS. For a constant PVP concentration and varying NaPSS concentration, the system remains stable until NaPSS is added in excess, which leads to depletion flocculation. Surface complex formation using the layer-by-layer technique was also reported at a planar silica interface.

Impact of End-Tethered Polyhedral Nanoparticles on the Mobility of Poly(dimethylsiloxane).

A series of dumbbell-shaped nanocomposite materials of poly(dimethylsiloxanes) (PDMSs) and polyhedral oligomeric silsesquioxanes (POSSs) were synthesized through hydrosilylation reactions of allyl- and vinyl-POSS and hydride-terminated PDMS. The chemical structures of the dumbbell-shaped materials, so-called POSS-PDMS-POSS triblocks, were characterized by (1)H NMR and FT-IR spectroscopy. The molecular weights of the triblock polymers were determined by gel permeation chromatography (GPC). Their size was analyzed by small-angle neutron scattering (SANS) and pulsed-field gradient stimulated echo (PFG STE) NMR experiments. The impact of POSS on the molecular mobility of the PDMS middle chain was observed by using (1)H spin-spin (T2) relaxation NMR. In contrast to the PDMS melts, the triblocks showed an increase in mobility with increasing molecular weight over the range studied due to the reduced relative concentration of constraints imposed by the end-tethered nanoparticles. The triblock systems were used to compare the impact of tethered nanoparticles on the mobility of the linear component compared to the mobility of the polymer in conventional blended nanocomposites. The tethered nanoparticles were found to provide more reinforcement than physically dispersed particles especially at high molecular weights (low particle concentration). The physical blends showed an apparent percolation threshold behavior.

Aggregation behavior of polyisoprene-pluronic graft copolymers in selective solvents.

Novel amphiphilic graft copolymers composed of a polyisoprene (PIP) backbone with Pluronic side chains, polyisoprene-g-Pluronic, have been synthesized using a "graft onto" technique. Small-angle neutron scattering (SANS) has been used to characterize the conformation of the P123 and P103 Pluronic graft copolymers in selective solvents such as ethanol and hexane and in a nonselective solvent, tetrahydrofuran (THF). The results indicated that, in a selective solvent for the side chain Pluronics (e.g., ethanol), "crew-cut" micelles were formed with a large core of radius ∼ 120 Å; data were fitted with a core-shell model. In a good solvent for the backbone (e.g., hexane), "flowerlike" micelles were formed with a small inner radius of ∼64 Å. In the nonselective solvent, a swollen polymer coil was found, which was described using the Guinier-Debye model. As THF/ethanol and THF/hexane can be prepared in any ratio, it was possible to vary the solvent composition gradually in order to study the transition from swollen coil to micelle. When going from 100% THF to 100% ethanol, the transition to micellar behavior was observed at a ratio of 20:80 (v/v %) THF/ethanol for both grafted copolymers and 40:60 (v/v %) THF/hexane for grafted P123 copolymers.

Adsorption and surfactant-mediated desorption of poly(vinylpyrrolidone) on plasma- and piranha-cleaned silica surfaces.

Optical flow cell reflectometry was used to study the adsorption of poly(vinylpyrrolidone) (PVP) to a silica surface and the subsequent surfactant adsorption and polymer desorption upon exposure to the anionic surfactant sodium dodecyl sulfate (SDS). We have studied these effects as a function of pH and surfactant concentration, but also for two different methods of silica preparation, O2 plasma and piranha cleaning. As a function of pH, a plateau in the amount adsorbed of ∼0.6 mg/m(2) is observed below a critical pH, above which the adsorption decreases to zero within 2-3 pH units. An increase in pH leads to dissociation of surface OH groups and a decreased potential for hydrogen bonding between the polymer and surface. For the plasma- and piranha-cleaned silica, the critical pH differs by 1-2 pH units, a reflection of the much larger amount of surface OH groups on piranha-cleaned silica (for a given pH). Subsequent rinsing of the adsorbed layer of PVP with an SDS solution leads to total or partial desorption of the PVP layer. Any remaining adsorbed PVP then acts as an adsorption site for SDS. A large difference between plasma- and piranha-cleaned silica is observed, with the PVP layer adsorbed to plasma-cleaned silica being much more susceptible to desorption by SDS. For a plasma-cleaned surface at pH 5.5, only 30% of the originally adsorbed PVP is remaining, while for piranha-cleaned silica, the pH can be increased to 10 before a similar reduction in the amount of adsorbed PVP is seen. For a given pH, piranha-cleaned silica has a higher surface charge, leading to a smaller amount of adsorbed SDS per PVP chain on a piranha-cleaned surface compared to a plasma-cleaned surface under identical conditions. In that way, the high negative surface charge makes desorption by negatively charged SDS more difficult. The high surface charge thus protects the neutral polymer from surfactant-mediated desorption.

More on polypseudorotaxanes formed between poly(ethylene glycol) and α-cyclodextrin.

A new interpretation for the mechanism associated with the spontaneous threading of α-CD, onto a PEG chain followed by the supramolecular hydrogel formation, is described. Beyond a specific stoichiometry, the complexation of α-CD and PEG results in the formation of a two-phase system. Besides the phase separation, for PEG with a molecular weight higher than 6000 Da, part of the polymer chains are unthreaded by the α-CD, leading to the formation of a supramolecular hydrogel. The kinetics for the complexation and the determination of the yield for equilibrated systems consisting of PEG (linear and star) are used to investigate the number of α-CD threaded before and after the phase separation. The results are compared with the prediction obtained from the application of the Poisson distribution and reveal the ratio between α-CD and PEG in each step of the process. Additionally, the kinetics for the hydrogel formation and its inner structure are investigated by using the proton NMR spin-spin relaxation of water.

Competition between polymers for adsorption on silica: a solvent relaxation NMR and small-angle neutron scattering study.

The competition between poly(vinylpyrrolidone) and poly(ethylene oxide) for adsorption at the silica surface was studied by solvent relaxation nuclear magnetic resonance and small-angle neutron scattering. The additive nature of the NMR relaxation rate enhancement was used to observe changes in the train layer when the two polymers were in direct competition for an increasing weight percentage of silica. PVP is shown to displace preadsorbed PEO from the particle surface, and this was observed for a range of PVP molecular weights. SANS measurements were found to give detailed information on the adsorption of the polymers in the separate systems; however, only qualitative information on the adsorption of the polymers could be obtained from the mixed samples. At a total polymer concentration of 0.4% w/v with 1.1% w/v silica, the SANS data were consistent with PVP adsorbing at the surface and dPEO remaining in solution, in agreement with the NMR data.

Surfactant-mediated desorption of polymer from the nanoparticle interface.

The surfactant-mediated desorption of adsorbed poly(vinylpyrrolidone), PVP, from anionic silica surfaces by sodium dodecyl sulfate, SDS, was observed. While photon correlation spectroscopy shows that the size of the polymer-surfactant-particle ensemble grows with added SDS, a reduction in the near-surface polymer concentration is measured by solvent relaxation NMR. Volume fraction profiles of the polymer layer extracted from small-angle neutron scattering experiments illustrate that the adsorbed polymer layer has become more diffuse and the polymer chains more elongated as a result of the addition of SDS. The total adsorbed amount is shown to decrease due to Coulombic repulsion between the surfactant-polymer complexes and between the complexes and the anionic silica surface.

Colloidal particles in competition for stabilizer: a solvent relaxation NMR study of polymer adsorption and desorption.

The competitive adsorption of poly(vinylpyrrolidone) onto silica and alumina-modified silica particles was studied using solvent relaxation nuclear magnetic resonance. The additive nature of the measured relaxation rate enabled predictions to be made of the relaxation rate in different polymer adsorption scenarios. Preferential adsorption of the poly(vinylpyrrolidone) onto the unmodified silica particles occurred when there was insufficient polymer in the system to coat the entire available surface area. Desorption was also found to occur when the polymer was initially adsorbed upon the alumina-modified particle and silica particles were added.

Manipulating interfacial polymer structures through mixed surfactant adsorption and complexation.

The effects of a nonionic alcohol ethoxylate surfactant, C(13)E(7), on the interactions between PVP and SDS both in the bulk and at the silica nanoparticle interface are studied by photon correlation spectroscopy, solvent relaxation NMR, SANS, and optical reflectometry. Our results confirmed that, in the absence of SDS, C(13)E(7) and PVP are noninteracting, while SDS interacts strongly both with PVP and C(13)E(7) . Studying interfacial interactions showed that the interfacial interactions of PVP with silica can be manipulated by varying the amounts of SDS and C(13)E(7) present. Upon SDS addition, the adsorbed layer thickness of PVP on silica increases due to Coulombic repulsion between micelles in the polymer layer. When C(13)E(7) is progressively added to the system, it forms mixed micelles with the complexed SDS, reducing the total charge per micelle and thus reducing the repulsion between micelle and the silica surface that would otherwise cause the PVP to desorb. This causes the amount of adsorbed polymer to increase with C(13)E(7) addition for the systems containing SDS, demonstrating that addition of C(13)E(7) hinders the SDS-mediated desorption of an adsorbed PVP layer.

Growth and shrinkage of pluronic micelles by uptake and release of flurbiprofen: variation of pH.

The micellization of Pluronic triblock copolymers (P103, P123, and L43) in the presence of flurbiprofen at different pH was studied by small-angle neutron scattering (SANS), pulsed-field gradient stimulated-echo nuclear magnetic resonance (PFGSE-NMR), and surface tension measurements. Addition of flurbiprofen to the Pluronic at low pH leads to an increase in the fraction of micellization, aggregation number, and the core radius of the micelles. However, changing the pH to above the pKa of flurbiprofen in an ethanol/water mixture (∼6.5) reduces the fraction of micellization and results in a weaker interaction between the drug and micelles due to the increased drug solubility in aqueous solution.

Flurbiprofen encapsulation using pluronic triblock copolymers.

Pulsed-field gradient stimulated-echo nuclear magnetic resonance (NMR) and surface tension measurements have been used to study the effect of drug addition on the micellization behavior of pluronic triblock copolymers (P103, P123, and L43). The addition of 0.6 wt% flurbiprofen to Pluronic P123 and P103 solutions reduced their cmc and promoted micellization. Also, a substantial increase in the hydrodynamic radius of Pluronic P103 from 5 to 10 nm was observed, along with an increased fraction of polymer micellized, demonstrating that the polymers solubilize this nonsteroidal anti-inflammatory drug.

Locus-specific microemulsion catalysts for sulfur mustard (HD) chemical warfare agent decontamination.

The rates of catalytic oxidative decontamination of the chemical warfare agent (CWA) sulfur mustard (HD, bis(2-chlororethyl) sulfide) and a range (chloroethyl) sulfide simulants of variable lipophilicity have been examined using a hydrogen peroxide-based microemulsion system. SANS (small-angle neutron scattering), SAXS (small-angle X-ray scattering), PGSE-NMR (pulsed-gradient spin-echo NMR), fluorescence quenching, and electrospray mass spectroscopy (ESI-MS) were implemented to examine the distribution of HD, its simulants, and their oxidation/hydrolysis products in a model oil-in-water microemulsion. These measurements not only present a means of interpreting decontamination rates but also a rationale for the design of oxidation catalysts for these toxic materials. Here we show that by localizing manganese-Schiff base catalysts at the oil droplet-water interface or within the droplet core, a range of (chloroethyl) sulfides, including HD, spanning some 7 orders of octanol-water partition coefficient (K(ow)), may be oxidized with equal efficacy using dilute (5 wt. % of aqueous phase) hydrogen peroxide as a noncorrosive, environmentally benign oxidant (e.g., t(1/2) (HD) approximately 18 s, (2-chloroethyl phenyl sulfide, C(6)H(5)SCH(2)CH(2)Cl) approximately 15 s, (thiodiglycol, S(CH(2)CH(2)OH)(2)) approximately 19 s {20 degrees C}). Our observations demonstrate that by programming catalyst lipophilicity to colocalize catalyst and substrate, the inherent compartmentalization of the microemulsion can be exploited to achieve enhanced rates of reaction or to exert control over product selectivity. A combination of SANS, ESI-MS and fluorescence quenching measurements indicate that the enhanced catalytic activity is due to the locus of the catalyst and not a result of partial hydrolysis of the substrate.

Not all anionic polyelectrolytes complex with DTAB.

The influence of hydroxypropyl guar (HPG), with and without boric acid, on dodecyltrimethyl ammonium bromide (DTAB) micellization was characterized by surface tension measurements, isothermal titration calorimetry, and small-angle neutron scattering. Although HPG is a nonionic water-soluble polymer, borate ions form weak bonds with HPG, transforming it into an anionic polyelectrolyte, HPG-borate. Surprisingly, the three independent measurements showed that HPG-borate does not promote DTAB micellization or phase separation normally seen when mixing oppositely charged polyelectrolytes and surfactants. However, the neutron scattering results suggested that HPG-borate binds to and flocculates existing DTAB micelles. The unusual behavior of HPG-borate with DTAB was underscored by showing that carboxymethyl guar (CMG) formed precipitates with DTAB.

Use of water spin-spin relaxation rate to probe the solvation of cyclodextrins in aqueous solutions.

1H spin-spin relaxation rate constant, R2, of water was measured by using the Carr-Purcell-Meiboom-Gill sequence in aqueous solutions of native cyclodextrins (alpha, beta, and gamma-CD) and chemically modified CDs in order to probe the structuring of the water surrounding these cyclic carbohydrate molecules. R2 values for water in solutions containing glucose and dextran were also measured for comparison. A two-site model for bonded and free water molecules was used to fit the results for the dependence of R2 on the solute concentrations. The order of relaxation rates for water in aqueous solution at a fixed specific hydroxyl group concentration is glucose>dextran congruent with CDs. No significant difference was observed for R2 of water in solutions containing native CDs, which indicates that the size and nature of the cavity has a small effect on the spin-spin relaxation times of water. The lower relaxation rate for water in CD solutions was attributed to the intramolecular hydrogen bonding formed between the secondary hydroxyl groups that line the rim of the CDs. For comparison, the relaxation rates for water in solutions of two chemically modified CDs were also studied.

Monodisperse emulsions from a microfluidic device, characterised by diffusion NMR.

A microfluidic device has been used to create novel monodisperse polymeric oil-in-water emulsions of diameter 15-100 µm, stabilised by surfactants and polymers. The pulse field gradient nuclear magnetic resonance (PFG-NMR) signal attenuation function showed minima that allow a simple calculation of the droplet size and polydispersity. The presence of the minima is due to the restricted diffusion of molecules within the droplets, which can be analysed using standard solutions of the diffusion equation with a spherical boundary condition. However, even when a small population of polymer is unrestricted, the deep troughs in the attenuation function are obscured. The simultaneous water NMR attenuation function gives structural information about the continuous-phase matrix. The NMR size measurements were compared with those obtained by optical and confocal microscopy, and laser diffraction analysis.

Solubility of cyclomaltooligosaccharides (cyclodextrins) in H2O and D2O: a comparative study.

Cyclomaltooligosaccharides (cyclodextrins, CDs) are cyclic oligomers having six, seven, or eight units of alpha-D-glucose, named as cyclomaltohexaose (alpha-CD), cyclomaltoheptaose (beta-CD) and cyclomaltooctaose (gamma-CD), respectively. The molecule of CD has a cavity in which the interior is hydrophobic relative to its outer surface. The solubility of cyclodextrins in water is unusual, as an irregular trend is observed in the series of the cyclic oligomers of glucose. beta-CD is at least nine times less soluble than the others CDs. This intriguing behavior has been investigated, and some interesting explanations in terms of the effect caused by CD on the water lattice structure have been proposed. In this work a comparative study on the solubility of alpha, beta, and gamma-cyclodextrins was carried out in H2O and D2O and reveals a much lower solubility of the three CDs in D2O. The solid-phase structure of the CDs in equilibrium with the solution is quite similar with both solvents. The results are discussed in terms of the CD molecular structure and the differences in the hydrogen bonds formed between H2O and D2O.

Effect of temperature, cosolvent, and added drug on Pluronic-flurbiprofen micellization.

Structural changes in the micellization of Pluronics P103 and P123, as a function of temperature, cosolvent (ethanol, 10 v/v %), and the addition of the hydrophobic drug flurbiprofen, were investigated by SANS and tensiometry. Addition of ethanol increases the critical micellization concentration of the Pluronics (making the polymer more soluble), while increasing the repulsive interactions between the flurbiprofen-Pluronic spherical complexes. However, increasing temperature and addition of drug increases both the aggregation number and core radius and leads to a more dehydrated core. The addition of flurbiprofen to Pluronic P103 was also found to reduce the critical micellization temperature from between 15 and 20 °C to below 10 °C and at higher drug concentrations leads to an attractive interaction between micelles and eventually phase separation.

Floating nematic phase in colloidal platelet-sphere mixtures.

The phase behaviour of colloidal dispersions is interesting for fundamental reasons and for technological applications such as photonic crystals and electronic paper. Sedimentation, which in everyday life is relevant from blood analysis to the shelf life of paint, is a means to determine phase boundaries by observing distinct layers in samples that are in sedimentation-diffusion equilibrium. However, disentangling the effects due to interparticle interactions, which generate the bulk phase diagram, from those due to gravity is a complex task. Here we show that a line in the space of chemical potentials µ(i), where i labels the species, represents a sedimented sample and that each crossing of this sedimentation path with a binodal generates an interface under gravity. Complex phase stacks can result, such as the sandwich of a floating nematic layer between top and bottom isotropic phases that we observed in a mixture of silica spheres and gibbsite platelets.

Measuring the structure of thin soft matter films under confinement: a surface-force type apparatus for neutron reflection, based on a flexible membrane approach.

A unique surface force type apparatus that allows the investigation of a confined thin film using neutron reflection is described. The central feature of the setup consists of a solid substrate (silicon) and a flexible polymer membrane (Melinex(®)). We show that inflation of the membrane against the solid surface provides close and even contact between the interfaces over a large surface area. Both heavy water and air can be completely squeezed out from between the flexible film and the solid substrate, leaving them in molecular contact. The strength of confinement is controlled by the pressure used to inflate the membrane. Dust provides a small problem for this approach as it can get trapped between membrane and substrate to prevent a small part of the membrane from making good contact with the substrate. This results in the measured neutron reflectivity containing a small component of an unwanted reflection, between 10% and 20% at low confining pressures (1 bar) and between 1% and 5% at high confining pressures (5 bar). However, we show that this extra signal does not prevent good and clear information on the structure of thin films being extracted from the neutron reflectivity. The effects of confinement are illustrated with data from a poly(vinyl pyrollidone) gel layer in water, a polyelectrolyte multilayer in water, and with data from a stack of supported lipid-bilayers swollen with D(2)O vapor. The data demonstrates the potential of this apparatus to provide information on the structure of thin films under confinement for a known confining pressure.