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International audience; Understanding the complex structure of polymer blends filled with nanoparticles (NPs) is the key to designing their macroscopic properties. Here, the spatial distribution of hydrogenated (H) and deuterated (D) polymer chains asymmetric in mass is studied by small-angle neutron scattering. Depending on the chain mass, a qualitatively new large-scale organization of poly(vinyl acetate) chains beyond the random-phase approximation is evidenced in nanocomposites with attractive polymersilica interactions. The silica is found to systematically induce bulk segregation. Only with long H-chains, a strong scattering signature is observed in the q-range of the NP size: it is the sign of interfacial isotopic enrichment, i.e., of contrasted polymer shells close to the NP surface. A quantitative model describing both the bulk segregation and the interfacial gradient (over ca. 10-20 nm depending on the NP size) is developed, showing that both are of comparable strength. In all cases, NP surfaces trap the polymer blend in a non-equilibrium state, with preferential adsorption around NPs only if chain length and isotopic preference towards the surface combine their entropic and enthalpic driving forces. This structural evidence for interfacial polymer gradients will open the road to quantitative understanding of the dynamics of many-chain nanocomposite systems.

International audience; Herein, we demonstrate that tuning of structural parameters and material chemistry enables control of the permeability and selectivity of gases (CO2, He, and CH4) in membranes based on poly(butyl methacrylate)-grafted nanoparticles (PGNs). Our data show that the presence of nanoparticles and the overall dense packing of grafted chains noticeable in PGNs with low grafting density have an adverse effect on the diffusivity of gases. This effect is compensated by an improvement in the solubility of CO2 gas promoted by the silica nanoparticle surface, yielding a substantial improvement in the permeability of CO2 versus CH4. In membranes with high grafting density, changes in the structural arrangements and alterations in the membrane porosity, evident from small-angle X-ray scattering and positron annihilation lifetime spectroscopy, positively influence the permeability of He and CO2 gases. In contrast, CH4 permeability in the same membranes is significantly suppressed, suggesting the formation of a unique, highly selective environment for gas separation. As a result, an improvement of up to 50% in selectivity for gas pairs containing large CH4 molecules is observed. Our studies provide fundamental insights into the role that structural parameters play in gas transport through polymer membranes, laying a foundation for the rational design of membranes with improved permeability and selectivity.

The structure of styrene–butadiene (SB) nanocomposites filled with industrial silica has been analyzed using electron microscopy and small-angle X-ray scattering. The grafting density per unit silica surface ρD3 was varied by adding graftable SB molecules. By comparing the filler structures at fixed ρD3 (so-called “twins”), a surprising match of the microstructures was evidenced. Mechanical measurements show that ρD3 also sets the modulus: it is then possible to tune the terminal relaxation time of nanocomposites via the chain length while leaving the modulus and structure unchanged.

International audience; Supramolecular associations provide a promising route to functional materials with properties such as self-healing, easy recyclability or extraordinary mechanical strength and toughness. The latter benefit especially from the transient character of the formed network, which enables dissipation of energy as well as regeneration of the internal structures. However, recent investigations revealed intrinsic limitations in the achievable mechanical enhancement. This manuscript presents studies of a set of telechelic polymers with hydrogen-bonding chain ends exhibiting an extraordinarily high, almost glass-like, rubbery plateau. This is ascribed to the segregation of the associative ends into clusters and formation of an interfacial layer surrounding these clusters. An approach adopted from the field of polymer nanocomposites provides a quantitative description of the data and reveals the strongly altered mechanical properties of the polymer in the interfacial layer. These results demonstrate how employing phase separating dynamic bonds can lead to the creation of high-performance materials.

International audience; Polymers with dynamic (transient) bonds, often called associating polymers, have been attracting significant attention in recent years due to their unique viscoelastic properties, self-healing ability, and recyclability. Nevertheless, understanding the mechanisms and the factors controlling their macroscopic properties remains limited due to the higher complexity introduced by the dynamic bonds. In this study, small-angle X-ray scattering (SAXS), broadband dielectric spectroscopy (BDS), and rheology were applied to unravel the structure and dynamics of telechelic associating polymers with different molecular weights. SAXS measurements revealed phase separation of the functional end groups with an average cluster size of ∼2–3 nm and the distance between clusters controlled by the chain length. Borrowing the interfacial layer model analysis of BDS data from the polymer nanocomposite field, we demonstrated the presence of an interfacial polymer layer with a thickness of ∼0.7–0.9 nm surrounding these clusters. Rheological measurements showed quantitatively that the presence of the interfacial layer significantly alters the viscoelastic behavior of these materials, indicating the crucial role of the interfacial layer in defining the macroscopic mechanical properties of the studied telechelic materials. The presented results emphasize that phase separation of the functional groups in associating polymers leads to very significant changes of the viscoelastic properties, opening a promising avenue in the design of novel functional materials.

International audience; Polymerized ionic liquids (PolyILs) are promising candidates for a broad range of technologies. However, the relatively low conductivity of PolyILs at room temperature has strongly limited their applications. In this work, we provide new insights into the roles of various microscopic parameters controlling ion transport in these polymers, which are crucial for their rational design and practical applications. Using broadband dielectric spectroscopy and neutron and light scattering techniques, we found a clear connection between the activation energy for conductivity, fast dynamics, and high-frequency shear modulus in PolyILs at their glass transition temperature (Tg). In particular, our analysis reveals a correlation between conductivity and the amplitude of fast picosecond fluctuations at Tg, suggesting the possible involvement of fast dynamics in lowering the energy barrier for ion conductivity. We also demonstrate that both the activation energy for ion transport and the amplitude of the fast fluctuations depend on the high-frequency shear moduli of PolyILs, thus identifying a practically important parameter for tuning conductivity. The parameters recognized in this work and their connection to the ionic conductivity of PolyILs set the stage for a deeper understanding of the mechanism of ion transport in PolyILs in the glassy state.

HAL Id: hal-02908124 https://hal.archives-ouvertes.fr/hal-02908124, The segmental dynamics of styrene–butadiene nanocomposites with embedded silica nanoparticles (NPs, ca. 20 vol. %) has been studied by broadband dielectric (BDS) and neutron spin–echo spectroscopy (NSE). It is shown by BDS that overlapping contributions only allow us to conclude on a range of distributions of relaxation times in simplified industrial nanocomposites formed with highly polydisperse NPs. For comparison, structurally similar but less aggregated colloidal nanocomposites have a well-defined distribution of relaxation times due to the reduced influence of interfacial polarization processes. This distribution is widened with respect to the neat polymer, without change in the position of the maximum and at most a small slowing down visible in the average time. We then demonstrate that incoherent NSE can be used to resolve small modifications of segmental dynamics of the industrial samples. By carefully choosing the q-vector of the measurement, experiments with fully hydrogenated polymer give access to the self-dynamics of the polymer in the presence of silica on the scale of approximately 1 nm. Our high-resolution measurements show that the segmental motion is slightly but systematically slowed also by the presence of the industrial filler NPs., The authors are thankful for support by the ANR NANODYN project, grant ANR-14-CE22-0001-01 of the French Agence Nationale de la Recherche.

International audience; The addition of hard fillers to a polymer matrix is a well-known process for achieving mechanical reinforcement. With a decrease in the size of the fillers, the contribution from polymer–particle nanometer-sized interfaces becomes significant, and these interfaces affect the mechanical performance of polymer nanocomposites (PNCs) beyond the limits established for conventional composites. However, the molecular mechanisms underlying the improvement in the mechanical performance of glassy PNCs remain unresolved, necessitating a deeper understanding of the structure–property relationships in these intrinsically heterogeneous systems. In this effort, by using Brillouin light scattering (BLS) and dynamic mechanical analysis (DMA), we demonstrated that adding shorter chains to a PNC prepared with high molecular weight polymers significantly improved the mechanical properties of the PNC in the glassy state. The strongest enhancement of mechanical properties occurred at an optimum concentration of short chains. This is in contrast to the behavior of the glass transition temperature of PNCs which shows a monotonic decrease with an increase in the concentration of shorter chains. Using experimental data and coarse-grained molecular dynamics (MD) simulations, we have identified the molecular mechanism leading to the observed nonmonotonic changes in mechanical reinforcement. This mechanism includes changes in the nanoscale organization at the interface combined with chain stretching amplified by the addition of the short chains. Overall, our approach paves a simple and cost-effective pathway to fabricating glassy PNCs with significantly improved mechanical properties that will fill various practical needs.

International audience; This paper presents an efficient way to measure the curing kinetics and gel point, αgel, in epoxy resins from one single experiment. The epoxy curing reaction is herein monitored using in situ and time-resolved near-infrared absorption spectroscopy (NIR). The curing profiles over different isothermal conditions are in good agreement with DSC. Furthermore, the increase of the NIR absorption bands of aromatic rings (unreactive throughout curing) probe the cure shrinkage, as more and more aromatic rings are localized within the fixed sample volume. Therefore, the gel point is determined using the onset of the aromatic absorption increase. The results are in good agreement with the theoretical gel point, as well as DMA results. This innovative approach enables gelation measurements on epoxy neat resins and film composites with an easy-to-perform, accurate, robust, and versatile method.

Despite the wide use of polymer nanocomposites (PNCs) in various applications, our understanding of the microscopic parameters controlling their macroscopic properties remains limited. In this study, we examine the dielectric strength of segmental dynamics, ΔeIL(T) in the interfacial polymer layer surrounding the nanoparticles in PNCs. The presented analysis reveals a significant drop in ΔeIL(T) and its anomalous temperature dependence in the polymer layer adsorbed to nanoparticles. The drop in ΔeIL(T) was observed in all samples regardless of whether segmental relaxation time in the interfacial layer was slower or faster than in the bulk polymer, excluding interpretation of the “dead” layer. We ascribe the observed decrease in the dielectric strength to the restricted amplitude of segmental relaxation in the interfacial/adsorbed layer. Our results provide a new perspective on discussion of dynamics in the interfacial layer in PNCs and thin polymer films, demonstrating that not only segmental relaxation time but also its amplitude can be strongly affected by the interface.

Industrial and model polymer nanocomposites are often formulated with coating agents (CAs) to improve polymer–nanoparticle (NP) compatibility. Here, the localization of silane CAs in the styrene–butadiene nanocomposite is investigated through the segmental dynamics of the polymer matrix by broadband dielectric spectroscopy (BDS), allowing the detection of silanes in the matrix through their plasticization effect. This acceleration of dynamics was followed via the shift of τmax of the α-relaxation induced by the presence of CAs of different molecular weights and quantities, for different amounts of incorporated colloidal silica NPs (R ≈ 12.5 nm, polydispersity 12%). Any noteworthy contribution of interfacial polymer layers to τmax has been excluded by reference measurements with bare NPs. Our approach allowed quantifying the partition between the matrix and the NP interfaces and was confirmed independently by calorimetry. As a control parameter, the silane-grafting reaction could be activated or not, which was confirmed by the absence (resp. presence) of partitioning with the matrix. Our main result is that in the first steps of material formulation, before any grafting reaction, CAs both cover the silica surface by adsorption and mix with the polymer matrix—in particular if the latter has chemical compatibility via its functional groups. Silane adsorption was found to be comparable to the grafted amount (1.1 nm–2) and does not increase further, confirming that the plateau of the adsorption isotherm is reached in industrial formulations. These results are hoped to contribute to a better understanding of the surface reactions taking place during complex formulation processes of nanocomposites, namely, the exact amounts at stake, for example, in industrial mixers. Final material properties are affected both through NP-matrix compatibility and plasticization of the latter by unreacted molecules., The authors are thankful for support by the ANR NANODYN project, grant ANR-14-CE22-0001-01 of the French Agence Nationale de la Recherche. They acknowledge financial support from the European Commission under the Seventh Framework Program by means of the grant agreement for the Integrated Infrastructure Initiative no. 262348 European Soft Matter Infrastructure (ESMI).

The antagonistic effect of processing and thermal annealing on both the filler structure and the polymer matrix is explored in polymer nanocomposites based on natural rubber with precipitated silica incorporated by coagulation from aqueous suspension followed by roll-milling. Their structure and linear and non-linear rheology have been studied, with a particular emphasis on the effect of high-temperature thermal treatment and the number of milling passes. Small-angle X-ray scattering intensities show that the silica is organized in small, unbreakable aggregates containing ca. 50 primary nanoparticles, which are reorganized on a larger scale in filler networks percolating at the highest silica contents. As expected, the filler network structure is found to be sensitive to milling, more milling inducing rupture, as evidenced by the decreasing Payne effect. After thermal treatment, the nanocomposite structure is found to be rejuvenated, erasing the effect of the previous milling on the low-strain modulus. In parallel, the dynamics of the samples described by the rheology or the calorimetric glass-transition temperature remain unchanged, whereas the natural latex polymer network structure is modified by milling towards a more fluid-like rheology, and cannot be recovered.

International audience; Recent experimental results using in particular small-angle scattering to characterize the self-assembly of mainly hard spherical nanoparticles into higher ordered structures ranging from fractal aggregates to ordered assemblies are reviewed. The crucial control of interparticle interactions is discussed, from chemical surface-modification, or the action of additives like depletion agents, to the generation of directional patches and the use of external fields. It is shown how the properties of interparticle interactions have been used to allow inducing and possibly controlling aggregation, opening the road to the generation of colloidal molecules or potentially metamaterials. In the last part, studies of the microstructure of polymer nanocomposites as an application of volume-spanning and stress-carrying aggregates are discussed.

International audience; Polymerized ionic liquids (PolyILs) are promising materials for applications in electrochemical devices spanning from fuel cells to capacitors and batteries. In principle, PolyILs have a competitive advantage over traditional electrolytes in being single ion conductors and thus enabling a transference number close to unity. Despite this perceived advantage, surprisingly low room temperature ionic conductivities measured in the lab raise an important fundamental question: how does the molecular structure mediate conductivity? In this work, wide-angle X-ray scattering (WAXS), vibrational sum frequency generation (vSFG), and density functional theory (DFT) calculations were used to study the bulk and interfacial structure of PolyILs, while broad band dielectric spectroscopy (BDS) was used to probe corresponding dynamics and conductive properties for a series of the PolyIL samples with tunable chemistries and structures. Our results reveal that the size of the mobile anions has a tremendous impact on chain packing in PolyILs that wasn’t addressed previously. Larger mobile ions tend to create a well-packed structure, while smaller ions frustrate chain packing. The magnitude of these changes and level of structural heterogeneity are shown to depend on the chemical functionality and flexibility of studied PolyILs. Furthermore, these experimental and computational results provide new insight into the correlation between conductivity and structure in PolyILs, suggesting that structural heterogeneity helps to reduce the activation energy for ionic conductivity in the glassy state.

The dynamic and static properties of the interfacial region between polymer and nanoparticles have wide-ranging consequences on performances of nanomaterials. The thickness and density of the static layer are particularly difficult to assess experimentally due to superimposing nanoparticle interactions. Here, we tune the dispersion of silica nanoparticles in nanocomposites by preadsorption of polymer layers in the precursor solutions, and by varying the molecular weight of the matrix chains. Nanocomposite structures ranging from ideal dispersion to repulsive order or various degrees of aggregation are generated and observed by small-angle scattering. Preadsorbed chains are found to promote ideal dispersion, before desorption in the late stages of nanocomposite formation. The microstructure of the interfacial polymer layer is characterized by detailed modeling of X-ray and neutron scattering. Only in ideally well-dispersed systems a static interfacial layer of reduced polymer density over a thickness of ca. 2 nm is evidenced based on the analysis with a form-free density profile optimized using numerical simulations. This interfacial gradient layer is found to be independent of the thickness of the initially adsorbed polymer, but appears to be generated by out-of-equilibrium packing and folding of the preadsorbed layer. The impact of annealing is investigated to study the approach of equilibrium, showing that initially ideally well-dispersed systems adopt a repulsive hard-sphere structure, while the static interfacial layer disappears. This study thus promotes the fundamental understanding of the interplay between effects which are decisive for macroscopic material properties: polymer-mediated interparticle interactions, and particle interfacial effects on the surrounding polymer.

The hysteretic softening at small dynamic strains (Payne effect)—related to the rolling resistance and viscoelastic losses of tires—was studied as a function of particle size, filler volume fraction, and temperature for carbon black (CB) reinforced uncrosslinked styrene–butadiene rubber (SBR) and a paste-like material composed of CB-filled paraffin oil. The low-strain limit for dynamic storage modulus was found to be remarkably similar for CB-filled oil and the CB-filled SBR. Small-angle X-ray scattering (SAXS) measurements on the simple composites and detailed data analysis confirmed that the aggregate structures and nature of filler branching/networking of carbon black were virtually identical within oil compared to the high molecular weight polymer matrix. The combined dynamic rheology and SAXS results provide clear evidence that the deformation-induced breaking (unjamming) of the filler network—characterized by filler–filler contacts that are percolated throughout the material—is the main cause for the Payne effect. However, the polymer matrix does play a secondary role as demonstrated by a reduction in Payne effect magnitude with increasing temperature for the CB-reinforced rubber, which was not observed to a significant extent for the oil–CB system.

Alumina-coated silica nanoparticles (NPs) grafted with phosphonic acids of different hydrophobicity were used as filler in poly(ethylacrylate) nanocomposites. Phosphonic acids bearing short alkyl chains or a diethylene glycol group have been grafted at densities up to 3.2 P/nm 2 on NPs (20 nm) dispersed in water. Nanocomposites at particle fractions up to 10 vol% have been formulated by casting from the colloidal mixtures of modified NPs and nanolatex in water. The dispersion of the NPs in the polymer matrix has been studied by TEM combined with small-angle scattering, evidencing aggregation of NPs. TEM shows micrometer-scale inhomogeneities depending on the surface/polymer matrix compatibility. For the local interparticle correlations, a quantitative analysis of the intensity based on the mapping onto the effective structure factor of polydisperse hard spheres is developed. This mapping allows the model-free determination of the internal volume fraction of aggregates, termed compacity κ, to between 10% and 30%, compatible with the TEM analysis. κ is found to increase for the higher particle volume fractions, to decrease with grafting density, and to be mostly independent of the nature and mass of the graft. Preliminary evidence for an improved compatibility of grafted with respect to bare NPs is found, as opposed to their aqueous precursor suspensions where some pre-aggregation is induced by grafting.

International audience; Despite an abundant literature on epoxy-amine systems, a complete description of the curing kinetics in epoxy-phenol composites was still lacking. In this study, the curing kinetics of an epoxy-phenol composite relevant to microelectronics industry is probed by isothermal and non-isothermal differential scanning calorimetry. An isoconversional analysis of the data reveals a significant contribution of the diffusion of molecular species to the activation energy, at low temperature and high degrees of curing. A model-fitting of the kinetics is performed in two successive steps: high-temperatures data are fitted with Arrhenius law and nth order autocatalytic model (where the diffusion contribution is neglected), whereas low-temperature data are fitted using Rabinowitch and modified-Williams-Landel-Ferry models (considering a diffusion contribution related to the glass transition). The chemical and diffusion contributions to the rate constants are calculated at various temperatures, clarifying the kinetics regimes with precision. Finally, the kinetics regimes are summarized in an improved time-temperature-transformation diagram.

International audience; A new method based on the combination of small-anglescattering, reverse Monte Carlo simulations, and an aggregate recognition algorithm is proposed to characterize the structure of nanoparticle suspensions in solvents and polymer nanocomposites, allowing detailedstudies of the impact of different nanoparticle surface modifications.Experimental small-angle scattering is reproduced using simulated annealing of configurations of polydisperse particles in a simulation box compatible with the lowest experimental q-vector. Then, properties of interest likeaggregation states are extracted from these configurations and averaged. This approach has been applied to silane surface-modified silica nanoparticles with different grafting groups, in solvents and after casting into polymer matrices.It is shown that the chemistry of the silane function, in particular mono- or trifunctionality possibly related to patch formation, affects the dispersion state in a given medium, in spite of an unchanged alkylchain length. Our approach may be applied to study any dispersion or aggregation state of nanoparticles. Concerningnanocomposites, the method has potential impact on the design of new formulations allowing controlled tuning of nanoparticle dispersion.

Quantitative characterization of the average structure of dense nanoparticle assemblies and aggregates is a common problem in nanoscience. Small-angle scattering is a suitable technique, but it is usually limited to not too big assemblies due to the limited experimental range, low concentrations to avoid interactions, and monodispersity to keep calculations tractable. In the present paper, a straightforward analysis of the generally available scattered intensity - even for large assemblies, at high concentrations - is detailed, providing information on the local volume fraction of polydisperse particles with hard sphere interactions. It is based on the identical local structure of infinite homogeneous nanoparticle assemblies and their subsets forming finite-sized clusters. This approach is extended to polydispersity, using Monte-Carlo simulations of hard and moderately sticky hard spheres. As a result, a simple relationship between the observed structure factor minimum - termed the correlation hole - and the average local volume fraction κ on the scale of neighboring particles is proposed and validated through independent aggregate simulations. This relationship shall be useful as an efficient tool for the structural analysis of arbitrarily aggregated colloidal systems.

International audience; An original protocol of simultaneous surface modification and transfer from aqueous to organic phases of anatase TiO2 nanoparticles (NPs) using alkylphosphonic acids (PAs) is studied. The influence of the solvent, the nature and concentration of the PA, and the size, concentration, and aggregation state of the TiO2 NPs was investigated. Complete transfer was observed for linear alkyl chains (5, 8, 12, and 18 C atoms), even at very high sol concentrations. After transfer, the grafted NPs were characterized by 31P solid-state MAS NMR. The dispersion state of NPs before and after phase transfer was monitored by dynamic light scattering (DLS). Small-angle neutron scattering (SANS) was used to characterize the structure of PA-grafted NPs in the organic solvent. Using a quantitative core?shell model cross-checked under different contrast conditions, it is found that the primary particles making up the NPs are homogeneously grafted with a solvated PA-layer. The nanometric thickness of the latter is shown to increase with the length of the linear carbon chain of the PA, independent of the size of the primary TiO2 NP. Interestingly, a reversible temperature-dependent aggregation was evidenced visually for C18PA, and confirmed by DLS and SANS: heating the sample induces the breakup of aggregates, which reassemble upon cooling. Finally, in the case of NPs agglomerated by playing with the pH or the salt concentration of the sols, the phase transfer with PA is capable of redispersing the agglomerates. This new and highly versatile method of NP surface modification with PAs and simultaneous transfer is thus well suited for obtaining well-dispersed grafted NPs.

We study the swelling and shrinking behavior of core-shell microgels adsorbed on silicon wafers. In these systems, the core is made of cross-linked poly(N-isopropylmethacrylamide) and the shell consists of cross-linked poly(N-n-propylacrylamide). In suspension, these particles exhibit an extended linear swelling behavior in the temperature interval between the lower critical solution temperatures of the two polymers. Using ellipsometry and atomic force microscopy, we show that this linear response is also observed in the adsorbed state.

The microstructure of polymer nanocomposites made with disordered silica filler (Zeosil(R) 1165MP) of industrial relevance and various coating agents is quantitatively analyzed using a combination of SAXS, TEM, and a recently developed structural model. The polymer matrix is formed by an end-functionalized styrene–butadiene statistical copolymer capable of covalent grafting on the silica nanoparticles. The effect of the coating agents with different alkyl chain length (C8, C12, and C18) on filler structure quantified in terms of aggregate formation, for different concentrations (up to 8 wt % with respect to silica), and the effect of a commonly added catalyzer, DPG, are studied using the structural model. As a result, we show that a strongly synergetic effect of both DPG and coating agent exists. Our findings open the road to a fundamental understanding and rational design of model and industrial nanocomposite formulation with optimized coating agents.

A large body of experimental work on the microstructure and dynamics of simplified industrial nanocomposites made of disordered silica filler in a styrene-butadiene matrix by solid-phase mixing is regrouped and critically discussed in this feature article. Recent results encompass systems with varying polymer mass, grafting functionality, and filler content. They have been obtained by simulation-based structural modelling of nanoparticle aggregate size and mass deduced from small-angle scattering and transmission electron microscopy. Our model has been validated by independent swelling experiments. Comparison of structurally-close nanocomposites of widely different chain mass led to the identification of a unique structure-determining parameter, the grafting density, as well as to a unified picture of aggregate formation mechanisms in complex nanocomposites during mixing. In addition, low-field proton NMR allowed for the characterization of dynamically slowed-down (‘glassy’) polymer layers, which were shown not to dominate the rheological response, unlike the structural contribution. Finally, broadband dielectric spectroscopy was used in an innovative manner to identify filler percolation – also identified by rheology – via dynamics along filler surfaces.

International audience; Polymer nanocomposites are used widely, mainly for the industrial application of car tyres. The rheological behavior of such nanocomposites depends in a crucial way on thedispersion of the hard filler particles – typically silica nanoparticles embedded in a soft polymer matrix. It is thus important to assess the filler structure, which may be quitedifficult for aggregates of nanoparticles of high polydispersity, and with strong interactions at high loading. This has been achieved recently using a coupled TEM/SAXSstructural model describing the filler microstructure of simplified industrial nanocomposites with grafted or ungrafted silica of high structural disorder. Here, wepresent an original method capable of reducing inter-aggregate interactions by swelling of nanocomposites, diluting the filler to low-volume fractions. Note that this isimpossible to reach by solid mixing due to the large differences in viscoelasticity between the composite and the pure polymer. By combining matrix crosslinking,swelling in a good monomer solvent, and post-polymerization of these monomers, it isshown that it is possible to separate the filler into small aggregates. The latter have then been characterized by electron microscopy and small-angle X-ray scattering,confirming the conclusions of the above mentioned TEM-SAXS structural model applied directly to the highly loaded cases.

We present a study on the structure and dynamics of poly(ethyl methacrylate) (PEMA), one of the polymers with shortest side-group in the poly(n-alkyl methacrylate)s (PnMAs) series. The contributions to the structure factor have been unveiled by combining T-dependent X-ray and neutron diffraction with polarization analysis on samples with different deuteration labelings, accessing thereby different partial structure factors of PEMA. We find clear hints for strong structural ordering with anticorrelated side-groups and main-chain locations, fitting thus in the general scenario of nanosegregation of main chains and side groups found in higher order PnMAs members. Backscattering measurements on a PEMA sample with deuterated side-group have revealed the dynamics of main-chain and α-methyl group hydrogens. The characterization of the rotations of the latter indicates highly disordered environments in the glassy state. Above the glass transition, the incoherent scattering function related to segmental relaxation shows stretching and clear deviations from Gaussian behavior in the accessed window. We also present results on the dynamic structure factor (collective dynamics) at the peaks characteristic (i) for the intermain-chain and interside-group-domain correlations and (ii) for the side-group/side-group atomic correlations within the domains. Viscosity dictates the temperature dependence in both cases, and also that of the dielectric spectroscopy results at high temperatures. However, the α-process followed by dielectric relaxation deviates from the rheological behavior when approaching the calorimetric glass-transition, indicating a strong influence of the faster side-group motions on the dynamics of the dielectric probes. © 2012 American Chemical Society., We thank support by the “Donostia International Physics Center”, the European Commission NoE SoftComp, Contract NMP3-CT-2004-502235, FP7-PEOPLE-2007-1-1-ITN (DYNACOP, EU), Projects MAT2007-63681 and IT-436-07 (GV) and the Spanish Ministerio de Educacion y Ciencia (Grant No. CSD2006-53). The European Commission, NMI3 Contract RII3-CT-2003-505925, supported the experiments at the Forschungsreaktor in Jülich, Germany.

International audience; The evolution of the polymer structure during nanocomposite formation and annealing of silica-latex nanocomposites is studied using contrast-variation small angle neutron scattering. The experimental system is made of silica nanoparticles (Rsi ≈ 8 nm) and a mixture of purpose-synthesized hydrogenated and deuterated nanolatex (Rlatex ≈ 12.5 nm). The progressive disappearance of the latex beads by chain interdiffusion and release in the nanocomposites is analyzed quantitatively with a model for the scattered intensity of hairy latex beads and an RPA description of the free chains. In silica-free matrices and nanocomposites of low silica content (7%v), the annealing procedure over weeks at up to Tg + 85 K results in a molecular dispersion of chains, the radius of gyration of which is reported. At higher silica content (20%v), chain interdiffusion seems to be slowed down on time-scales of weeks, reaching a molecular dispersion only at the strongest annealing. Chain radii of gyration are found to be unaffected by the presence of the silica filler.

International audience; The conformation of poly(ethyl methacrylate) chains in silica–latex nanocomposites has been studied under zero average contrast conditions (ZAC) using small-angle neutron scattering (SANS). Samples have been prepared by drying colloidal suspensions of silica and polymer nanoparticles (NPs) followed by thermal annealing, for two different silica NPs (radius of 5 and 15 nm) and two chain molecular weights (17 and 100 kg/mol). By appropriate mixing of hydrogenated and deuterated polymer, chain scattering contrast is introduced, and in principle silica scattering suppressed. The silica structure consisting mostly of small fractal aggregates is characterized by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) on the same samples. The measurement of the chain structure by SANS, however, is perturbed by unwanted silica contributions, as often reported in the literature. Here, the contribution of contrast-matched silica is evidenced as a function of system parameters, namely chain mass, silica size, and volume fraction, and a model rationalizing these contributions for the first time is proposed. On the basis of a statistical analysis, a nanometer-thick polymer shell surrounding silica NPs is shown to create contrast, which is presumably maintained by the reduced mobility of polymer close to interfaces or attractive polymer–silica interactions. This shell is proven to be quantitatively important only for the smallest silica NPs. Finally, the pure polymer scattering can be isolated, and the polymer radius of gyration is found to be independent of filler content and NP size.

The structure and dynamics of filler nanoparticles and macromolecules in polymer nanocomposites determine many aspects of macroscopic behavior, which is why these properties have attracted considerable interest in the scientific literature. In this article, recent progress using scattering techniques for the elucidation of structure and dynamics, of both filler nanoparticles and polymer chains, is reviewed. Small-angle X-ray and neutron scattering, more and more combined with direct imaging methods and simulations, are appropriate methods to investigate nanocomposite structure. While they can usually be applied to standard samples for filler structure, chain structure can only be accessed with neutrons and isotopic substitution, under the zero-average contrast condition to match the filler contribution. Quasi-elastic neutron scattering and X-ray photon correlation spectroscopy cover different time scales with spatial resolution in the nanoscale. The former allows studies of polymer motions from atomic or segmental relaxation to reptation of the entire chain in the presence of filler, while the latter is increasingly used for investigations of nanoparticle dynamics.

International audience; It is often necessary to tailor nanoparticle (NP) interactions and their compatibility with a polymer matrix by grafting organic groups, but the commonly used silanization route offers little versatility, particularly in water. Herein, alumina-coated silica NPs in aqueous sols have been modified for the first time with low molecular-weight phosphonic acids (PAs) bearing organic groups of various hydrophobicities and charges: propyl, pentyl and octyl PAs, and two PAs bearing hydrophilic groups, either a neutraldiethylene glycol (DEPA) or a potentially charged carboxylic acid (CAPA) group. The interactions and aggregation in the sols have been investigated using zeta potential measurements, dynamic light scattering, transmission electron microscopy, and small-angle scattering methods. The surface modification has been studied using FTIR and 31P MAS NMR spectroscopies. Both high grafting density r and high hydrophobicity of the groups on the PAs induced aggregation, whereas suspensions of NPsgrafted by DEPA remained stable up to the highestr . Unexpectedly, CAPA-modified NPs showedaggregation even at low r, suggesting that the carboxylic end group was also grafted to the surface. Surface modification of aqueous sols with PAs allows thus for the grafting of a higher density and a wider variety of organic groups than organosilanes, offering an increased control of the interactions between NPs, which is of interest for designing waterborne nanocomposites.

The dynamics of polymer and filler in simplified industrial silica-styrene-butadiene nanocomposites (silica Zeosil 1165 MP, volume fraction 0-21%v) have been studied with broadband dielectric spectroscopy (BDS) and nuclear magnetic resonance (NMR). The fraction of graftable matrix chains was varied from 0 to 100%D3. The introduction of silica nanoparticles is shown to leave the segmental relaxation unaffected, an observation confirmed by the measurement of only a thin (some Angstroms thick) immobilized layer by NMR. The low-frequency measurements are resolved in two distinct dielectric Maxwell-Wagner-Sillars (MWS) processes of different behavior with respect to changes of large-scale silica structures induced by variations of filler fraction and grafting. It is found that increasing grafting leaves the first MWS-process unaffected, while it decreases the strength of the (slower) second MWS by about a decade. At constant silica volume fraction, this indicates depercolation of the filler, thereby providing a microscopic explanation of the evolution of rheological reinforcement. The sensitivity to large-scale reorganizations together with a characterization of local polymer dynamics provides insight over many length- and time-scales into structure and dynamics of nanocomposites, and thus the physical origin of the reinforcement effect., We are thankful for a “Chercheur d'Avenir” grant by the Languedoc-Roussillon region (J.O.) and Ph.D. funding “CIFRE” by Michelin (G.P.B.). The authors acknowledge financial support from the European Commission under the Seventh Framework Program by means of the grant agreement for the Integrated Infrastructure Initiative N. 262348 European Soft Matter Infrastructure (ESMI).

The existence of two independent filler-dependent high-temperature Maxwell-Wagner-Sillars (MWS) dielectric processes is demonstrated and characterized in detail in silica-filled styrene-butadiene (SB) industrial nanocomposites of simplified composition using Broadband Dielectric Spectroscopy (BDS). The uncrosslinked samples are made with 140 kg mol-1 SB-chains, half of which carry a single graftable end-function (50% D3), and Zeosil 1165 MP silica incorporated by solid-phase mixing. While one high-temperature process is known to exist in other systems, the dielectric properties of a new silica-related process - strength, relaxation time, and activation energy - have been evidenced and described as a function of silica volume fraction and temperature. In particular, it is shown that its strength follows a percolation behavior as observed with the ionic conductivity and rheology. Moreover, activation energies show the role of polymer layers separating aggregates even when they are percolated. Apart from simultaneous characterization over a broad frequency range up to local polymer and silanol dynamics, it is believed that such high-temperature BDS-measurements can thus be used to detect reorganizations in structurally-complex silica nanocomposites. Moreover, they should contribute to a better identification of dynamical processes via the described sensitivity to structure in such systems., We are thankful for a ‘‘Chercheur d’Avenir’’ grant by the Languedoc-Roussillon region (J.O.) and PhD funding ‘‘CIFRE’’ by Michelin (G.P.B.). The authors acknowledge financial support from the European Commission under the Seventh Framework Program by means of the grant agreement for the Integrated Infrastructure Initiative No. 262348 European Soft Matter Infrastructure (ESMI).

We have investigated the molecular dynamics of syndiotactic poly(methyl methacrylate) well above the glass transition by combining quasielastic neutron scattering and fully atomistic computer simulations. The incoherent scattering measured by backscattering on a sample with deuterated ester methyl groups has revealed the single-particle motions of hydrogens in the main chain and in the α-methyl groups. Moreover, with neutron spin-echo experiments on the fully deuterated sample we have accessed the collective motions at the two first maxima of the structure factor. The simulated cell, which has been previously validated regarding the structural properties [Genix, A.-C.; et al. Macromolecules2006, 39, 3947], shows a dynamical behavior that, allowing a shift in temperature, reproduces very accurately all the experimental results. The combined analysis of both sets of data has shown that: (i) The segmental relaxation involving backbone atoms deviates from Gaussian behavior. (ii) The dynamics is extremely heterogeneous: in addition to the subdiffusion associated with the α-process and the methyl group rotations, we have found indications of a rotational motion of the ester side group around the main chain. (iii) At a given momentum transfer and depending on the molecular groups considered, the time scales for collective motion are spread over about 1 order of magnitude, the correlations involving the main chain decaying much more slowly than those relating side groups. (iv) At the length scale characteristic for the overall periodicity of the system (that corresponding to the first structure factor peak), the experimentally observed collective dynamics relates to the backbone motions and is of interchain character; there, coherency effects are observed for all correlations, though side groups display weaker collectivity. (v) At the second structure factor peak, coherency remains only for correlations involving the main chains., This research project has been supported by the European Commission NoE SoftComp, Contract NMP3-CT-2004-502235. A.A., F.A., and J.C. acknowledge support from the projects MAT2004-01017 and 9/UPV00206.215-13568/2001. “Donostia International Physics Center” is also acknowledged. The European Commission, NMI3 Contract RII3-CT-2003-505925, supported the experiments at the Forschungsreaktor in Jülich.

International audience; The formation of aggregates in simplified industrial styrene–butadiene nanocomposites with silica filler hasbeen studied using a recent model based on a combination of electron microscopy, computer simulations,and small-angle X-ray scattering. The influence of the chain mass (40 to 280 kg/mol, PI < 1.1), which setsthe linear rheology of the samples, was investigated for a low (9.5 vol%) and high (19 vol%) silica volumefraction. 50% of the chains bear a single graftable end-group, and it is shown that the (chain-massdependent) grafting density is the structure-determining parameter. A model unifying all available dataon this system is proposed and used to determine a critical aggregate grafting density. The latter is foundto be closely related to the mushroom-to-brush transition of the grafted layer. To our best knowledge,this is the first comprehensive evidence for the control of the complex nanoparticle aggregate structurein nanocomposites of industrial relevance by the physical parameters of the grafted layer.

International audience; The structure of silica-latex nanocomposites of three matrix chain masses (20, 50, and 160 kg/mol of poly(ethyl methacrylate)) are studied using a SAXS/TEM approach, coupled via Monte Carlo simulations of scattering of fully polydisperse silica nanoparticle aggregates. At low silica concentrations (1 vol. %), the impact of the matrix chain mass on the structure is quantified in terms of the aggregation number distribution function, highest mass leading to individual dispersion, whereas the lower masses favor the formation of small aggregates. Both simulations for SAXS and TEM give compatible aggregate compacities around 10 vol. %, indicating that the construction algorithm for aggregates is realistic. Our results on structure are rationalized in terms of the critical collision time between nanoparticles due to diffusion in viscous matrices. At higher concentrations, aggregates overlap and form a percolated network, with a smaller and lighter mesh in the presence of high mass polymers. The linear rheology is investigated with oscillatory shear experiments. It shows a feature related to the silica structure at low frequencies, the amplitude of which can be described by two power laws separated by the percolation threshold of aggregates.

International audience; An un-cross-linked SBR-system filled with precipitated silica nanoparticles of radius ≈10 nm by mixing is studied as a function of the fraction of graftable matrix chains (140 kg mol-1) varying from 0% to 100%, for a low (ΦSi = 8.5 vol %) and high (16.7 vol %) silica volume fraction. The linear rheology in shear shows a strong impact of the grafting on the terminal flow regime, and a shift to longer relaxation times with increasing grafting. Simultaneously, the plateau modulus stays approximately constant for the low ΦSi, suggesting a link to the silica content. The microstructure of the silica is characterized by using a combination of transmission electron microscopy and small-angle X-ray scattering data. We apply a quantitative model of interacting aggregates, and determine the average aggregation number (decreasing from 160 to 30 with grafting), aggregate size (50 to 30 nm), and compacity (55% to 35%). While the linear rheology seems to be dominated by the matrix composition, both the mixing rheology and the structure display a saturation with increasing grafting fraction. A closer analysis of this effect indicates that a critical amount of grafting is needed to trigger structural evolution. To summarize, a quantitative study of complex nanocomposites with several features of industrial systems demonstrates that the grafting density can be used as a fine-tuning parameter of rheology and microstructure.

International audience; Simplified silica (Zeosil 1165 MP) and SBR (140k carrying silanol end-groups) nanocomposites have been formulated by mixing of a reduced number of ingredients with respect to industrial applications. The thermo-mechanical history of the samples during the mixing process was monitored and adjusted to identical final temperatures. The filler structure on large scales up to micrometers was studied by transmission electron microscopy (TEM) and very small-angle X-ray scattering (SAXS). A complete quantitative model extending from the primary silica nanoparticle (of radius ≈10 nm), to nanoparticles aggregates, up to micrometer-sized branches with typical lateral dimension of 150 nm is proposed. Image analysis of the TEM-pictures yields the fraction of zones of pure polymer, which extend between the branches of a large-scale filler network. This network is compatible with a fractal of average dimension 2.4 as measured by scattering. On smaller length scales, inside the branches, small silica aggregates are present. Their average radius has been deduced from a Kratky analysis, and it ranges between 35 and 40 nm for all silica fractions investigated here (Φsi = 8−21% vol.). A central piece of our analysis is the description of the interaggregate interaction by a simulated structure factor for polydisperse spheres representing aggregates. A polydispersity of 30% in aggregate size is assumed, and interactions between these aggregates are described with a hard core repulsive potential. The same distribution in size is used to evaluate the polydisperse form factor. Comparison with the experimental intensity leads to the determination of the average aggregate compacity (assumed identical for all aggregates in the distribution, between 31% and 38% depending on Φsi), and thus aggregation number (ca. 45, with a large spread). Because of the effect of aggregate compacity and of pure polymer zones, the volume fraction of aggregates is higher in the branches than Φsi. The repulsion between aggregates has a strong effect on the apparent isothermal compressibility: it leads to a characteristic low-q depression, which cannot be interpreted as aggregate mass decrease in our data. In addition, the reinforcement effect of these silica structures in the SBR-matrix is characterized with oscillatory shear and described with a model based on the same aggregate compacity. Finally, our results show that it is possible to analyze the complex structure of interacting aggregates in nanocomposites of industrial origin in a self-consistent and quantitative manner.

By means of quasielastic neutron scattering we have investigated the hydrogen dynamics in poly(alkylene oxide)s (PAOs) with different side-chain lengths at temperatures below as well as above the glass-transition. The combination of results from three different spectrometers (a time-of-flight and two backscattering instruments) has allowed covering almost 4 orders of magnitude in time - from the ps to ns range - with spatial resolution. The results evidence the simultaneous occurrence of vibrations and localized side-group motions at low temperatures and additional diffusive-like (segmental) dynamics at high temperatures. The localized processes of the side groups show (i) stretching of the scattering function, (ii) associated activation energies similar to those found for single and cooperative bond rotations of polyethylene, and (iii) spatial extents that increase with increasing temperature. Compared with poly(ethylene oxide) (PEO), the diffusive segmental process in PAOs presents (i) the same spectral shape, (ii) slower characteristic times - antiplasticization - (iii) similar deviations from Gaussian behavior. For comparison, we also report on backscattering results on the side-group dynamics of poly(n-hexyl methacrylate) in the same temperature range, that show evidence for confinement effects. We suggest that the dynamic asymmetry in systems with intrinsic dynamic heterogeneities between constituent parts is the key ingredient leading to both plasticization and confinement effects. © 2012 American Chemical Society., This research at Oak Ridge National Laboratory’s Spallation Neutron Source was partially sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. C.G. acknowledges financial support by the International Helmholtz Research School of Biophysics and Soft Matter (IHRS BioSoft). We acknowledge support by the “Donostia International Physics Center”, the European Commission NoE SoftComp, Contract NMP3-CT-2004-502235, FP7-PEOPLE-2007-1-1-ITN (DYNACOP, EU), the projects MAT2007-63681, IT-436-07 (GV), and the Spanish Ministerio de Educacion y Ciencia (Grant No. CSD2006-53).

The tunable structure of silica-latex nanocomposites made of silica nanoparticles (radius ≈ 80 Å) and a copolymer of methyl methacrylate and butyl acrylate-latex beads (radius≈210 Å) has been studied by small-angle neutron scattering and transmission electron microscopy. An aggregation diagram as a function of the control parameters--silica volume fraction and precursor solution pH--has been established. In this aggregation diagram, isoaggregation lines have been identified. It was used to express the small-strain reinforcement factor measured with stress-strain isotherms as a function of volume fraction at fixed aggregation number in the range from 50 to 100. The large-strain properties have been rationalized using the energy needed to rupture samples, and this quantity has been found to present an optimum at intermediate volume fractions (15%). In order to understand the striking rheology of the system, a neutron contrast-matching study has been undertaken by adding deuterated polymer beads. The bead demixing kinetics during annealing has been used to characterize the dynamics in various environments defined by the hard silica structure. In particular, in nanocomposite samples containing 15 vol % of silica the dynamics is found to be blocked.

13 páginas, 15 figuras, 4 tablas.-- El pdf del artículo es la versión post-print., Combining neutron diffraction, neutron spin echo, differential scanning calorimetry, and dielectric spectroscopy, we have investigated the structure and dynamics of poly(n-butyl methacrylate) (PBMA) and poly(n-hexyl methacrylate) (PHMA). Signatures of the occurrence of a glass transition associated with the freezing of the intermolecular correlations within alkyl nanodomains are present in the structural data. Exploiting isotopic labeling, neutron scattering has revealed collective dynamics at the main-chain and side-group levels for both polymers and the self-motions of hydrogen atoms in the side groups of PHMA, adding valuable microscopic information to comprehensive relaxation maps and putting the relaxation results into a perspective. Moreover, we find exotic dynamical behavior for the side groups, characterized by extremely stretched (nearly logarithmic-like) decays of the correlation functions. For PHMA, a complete dynamical decoupling of side-group dynamics from the main-chain motions is found. The side groups of this polymer show an extremely “strong” temperature dependence of the structural relaxation time and much faster characteristic times for self than collective motions. The analogies found between the self-motions of the side-group H atoms in PHMA and the γ-relaxation process in semicrystalline polyethylene (PE) strengthen the picture of confined PE-like dynamics within alkyl nanodomains. We discuss possible origins for the observed phenomenology., This research project has been supported by the European Commission NoE SoftComp, Contract NMP3-CT-2004-502235, the “Donostia International Physics Center”. A.A. and J.C. acknowledge support from the projects MAT2007-63681, IT-436-07 (GV), and the Spanish Ministerio de Educacion y Ciencia (Grant CSD2006-53).

We have exploited the selectivity of neutron scattering combined with isotopic substitution to study the structure and dynamics of poly(n-alkyl methacrylates). Our diffraction data strongly support the suggested nanosegregation of main-chains and side groups. Moreover, we have been able to separately follow the dynamics of both subsystems at a molecular scale. While the structural relaxation observed at the main-chain level is standard, for high-order members the correlations involving side groups within the alkyl nanodomains relax through an exotic logarithmic decay. In these polymers, a strong dynamic asymmetry also develops. We discuss possible theoretical frameworks for the anomalous relaxation observed., We thank the ILL scientists M. Maccarini, B. Deme and P. P. Deen for experimental help, and the NoE SoftComp, Contract NMP3-CT-2004-502235, ‘Donostia International Physics Center’, the projects MAT2007-63681, IT-436-07 (GV) and the Spanish Ministerio de Educacion y Ciencia (CSD2006-53) for financial support.

The local structure of syndiotactic poly(methyl methacrylate) (PMMA) has been investigated by combining neutron scattering and fully atomistic molecular dynamics simulations. Selectively deuterating parts of the PMMA monomer, we have accessed five different partial structure factors in the glassy state by neutrons, and polarization analysis has allowed isolating the coherent contribution to the total scattering. In addition, the temperature dependence of the static structure factor has been determined on the fully deuterated sample. The different measured partial structure factors show qualitatively different features with respect to peak positions and heights and provide a very critical check to validate the simulated structure. To gain deep insight into the structure, we have grouped the simulation results in terms of three molecular substructures: the main chain, the α-methyl group, and the ester side group. The study of the resulting partial structure functions has revealed the origin of the diffraction peaks, including those in the X-rays pattern reported in the literature. In addition, a real-space evaluation of the characteristic radial distribution functions has allowed separating intra- and interchain contributions to the total correlation functions. We have found that (i) PMMA exhibits a strong local order with an average main-chain distance of ≈8.6 Å, (ii) this is the only average interchain distance and thus no precursor effect of a layered structure is found, (iii) the main chain shows a persisting all-trans structure, and (iv) a strong anticorrelation between the main chain and the ester side groups, together with an interdigitation of the side groups, suggests a marked separation between the backbone and the side-group spatial arrangements., This research project has been supported by the European Commission NoE SoftComp, Contract NMP3-CT-2004-502235. A.A., F.A., and J.C. acknowledge support from the projects MAT2004-01017 and 9/UPV00206.215-13568/2001. “Donostia International Physics Center” is also acknowledged. The European Commission, NMI3 Contract RII3-CT-2003-505925, supported the experiments at the Forschungsreaktor in Jülich