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The structure and properties of polysiloxane dendrimer melts are studied by extensive atomistic molecular dynamics simulations. Two homologous series differing in the spacer length are considered. In the first series the dendrimer spacers are the shortest ones, comprising only one oxygen atom, while in the second series the spacers consist of two oxygen atoms with the silicon atom in between. Melts of the dendrimers from the 3rd up to the 6th generation number are modelled in a wide temperature range from 273 to 600 K. A comparative study of the macroscopic melt characteristics such as the melt density and thermal expansion coefficients is performed for the two series. Analysis of the dendrimer structure in melts and in the isolated state shows that intermolecular interactions and interpenetration of dendrimer molecules in melts hardly affect the dendrimer interior organization. However, the presence of neighboring molecules significantly slows down their intramolecular dynamics in melts in comparison with that of isolated dendrimers. An increasing generation number causes an increase of the radius of the dendrimer interior region unavailable for neighboring molecules, which starts to exceed the length of the peripheral interpenetration layer for high-generation dendrimers; this fact could lead to different mechanisms of melt dynamics for lower and higher generation dendrimers.

Here we report on a light triggered remote control of microgel size in the presence of photosensitive surfactant. The hydrophobic tail of the cationic surfactant contains azobenzene group that undergoes a reversible photo-isomerization reaction from a trans-to a cis-state accompanied by a change in the hydrophobicity of the surfactant. We have investigated light assisted behaviour and the complex formation of the microgels with azobenzene containing surfactant over the broad concentrational range starting far below and exceeding several times of the critical micelle concentration (CMC). At small surfactant concentration in solution (far below CMC), the surfactant in the trans-state accommodates within the microgel causing its compaction, while the cis-isomer desorbs out of microgel resulting in its swelling. The process of the microgel size change can be described as swelling on UV irradiation (trans-cis isomerization) and shrinking on irradiation with blue light (cis-trans isomerization). However, at the surfactant concentrations larger than CMC, the opposite behaviour is observed: the microgel swells on blue irradiation and shrinks during exposure to UV light. We explain this behaviour theoretically taking into account isomer dependent micellization of surfactant within the microgels. Published by AIP Publishing.

A series of copolymers with controlled monomer sequences are prepared via the reversible addition–fragmentation chain transfer polymerization of tert-butyl carbamate (Boc)-l-alanine (VBA) and Boc-l...

Dielectric properties of two series of magnetoactive elastomers (MAEs) based on a soft silicone matrix containing 35 vol% of magnetic particles were studied experimentally in a wide temperature range. In the first series, a hybrid filler representing a mixture of magnetically hard NdFeB particles of irregular shape and an average size of 50 μm and magnetically soft carbonyl iron (CI) of 4.5 μm in diameter was used for MAE fabrication. MAEs of the second series contained only NdFeB particles. The presence of magnetically hard NdFeB filler made it possible to passively control MAE dielectric response by magnetizing the samples. It was shown that although the hopping mechanism of MAEs conductivity did not change upon magnetization, a significant component of DC conductivity appeared in the magnetized MAEs presumably due to denser clustering of interacting particles resulting in decreasing interparticle distances. The transition from a non-conducting to a conducting state was more pronounced for hybrid MAEs containing both NdFeB and Fe particles with a tenfold size mismatch. Hybrid MAEs also demonstrated a considerable increase in the real part of the complex relative permittivity upon magnetization and its asymmetric behavior in external magnetic fields of various directions. The effects of magnetic filler composition and magnetization field on the dielectric properties of MAEs are important for practical applications of MAEs as elements with a tunable dielectric response.

International audience; The instability of a homogeneous complex coacervate phase induced by incompatibility of oppositely charged polyelectrolytes is studied by means of the random phase approximation (RPA) and the scaling approach. It is found that in a poor solvent for both polyions their short-range mutual repulsions may result in the formation of a microphase separated structure at low salt concentrations cs. At high cs, a decomposition of the homogeneous coacervate into two macroscopic globular phases enriched either with polyanions or with polycations takes place. Both the RPA and scaling estimations predict the period of the microphase separated structure on the order of a few nanometers in the vicinity of the spinodal. The binodal of macroscopic phase separation of the coacervate and the spinodal with respect to the microphase separation are calculated, and the phase diagram of the coacervate is constructed in terms of salt concentration and incompatibility of polyions. The possibility of experimental observation of a microsegregated coacervate is discussed.

A series of magnetoactive elastomer (MAE) coatings consisting of a silicone matrix and carbonyl iron particles (3–5 μm in diameter) have been synthesized and their hydrophobic properties have been investigated in various magnetic fields of disk-shaped permanent NdFeB magnets. Concentration of magnetic filler in MAEs has been varied in the range of 63–76 mass%. Both isotropic samples and structured samples synthesized in the magnetic field of 80 mT have been obtained. It has been shown that application of a magnetic field induces structuring of the filler on the surface of MAE coatings, resulting in formation of mountain-like microstructures. Microstructure relief on coating surfaces leads to an increase of a water contact angle which could be varied from 110° ± 10° at zero field up to 163° ± 2° at 600 mT. The contact angle at the maximum field increases with iron filler content and with softening of the polymer matrix.

Rheological melt behavior of carbosilane dendrimers from the 3rd up to the 8th generation has been studied experimentally under steady shear, creep and dynamic oscillatory shear. Six orders of magnitude jump in viscosity was found between the 5th and the 6th generations. While the low-generation dendrimer melts demonstrate Newtonian behavior in a wide temperature range of 20÷80 °C, starting from the 6 t h generation, the dendrimer melts lose their ability to freely flow and acquire properties of a material with a well-pronounced yield stress. The storage modulus of high-generation dendrimer melts by far exceeds the loss modulus, furthermore, its value increases with temperature. It is demonstrated that the high-generation carbosilane dendrimers in bulk can be considered a polymer material with unique properties and as that, could find new applications in high-tech areas, in particular, as matrices for sensors.

Magnetodielectric properties of magnetoactive elastomers comprising micrometer-sized iron particles dispersed in compliant elastomer matrices are experimentally studied in stepwise time-varying dc magnetic fields. It is found that imposition of magnetic field significantly increases both the effective lossless permittivity of these composite materials as well as their effective conductivity. These magnetodielectric effects are more pronounced for larger concentrations of soft-magnetic filler particles and softer elastomer matrices. The largest observed relative change of the effective dielectric constant in the maximum magnetic field of 0.57 T is of the order of 1000%. The largest observed absolute change of the loss tangent is approximately 0.8. The transient response of the magnetodielectric effect to a step magnetic-field excitation can be rather complex. It changes from a simple monotonic growth with time for small magnetic-field steps ( 0.3 T). The settling time to the magnetic-field step excitation can reach roughly 1000 s and it depends on the applied magnetic field and sample composition. There is also significant hysteresis of the magnetodielectric effect on the externally applied magnetic field. These findings are attributed to the rearrangement of ferromagnetic filler particles in external magnetic fields. The results will be useful for understanding and predicting the transient behavior of magnetoactive elastomers in applications where the control magnetic field is time dependent.

The phenomenon of spinodal decomposition in weakly charged polyelectrolyte solutions is studied theoretically within the random phase approximation. A novel feature of the theoretical approach is that it accounts for the effects of ionic association, i.e. ion pair and multiplet formation between counterions and ions in polymer chains, as well as the dependence of local dielectric permittivity on the polymer volume fraction Φ. The main focus is on the spinodal instability of polyelectrolyte solutions towards microscopic phase separation. It has been shown that increasing the binding energy of ions decreases the classical microphase separation region (possible at low polymer concentrations) due to the effective neutralization of the chains. A qualitatively new type of microphase separation is found in the presence of a dielectric mismatch between polymer and solvent. This new branch of microphase separation is realized at high polymer concentrations where ion association processes are the most pronounced. Typical microstructures are shown to have a period of a few nanometers like in ionomers. The driving force for the microphase formation of a new type is more favourable ion association in polymer-rich domains where ionomer-type behavior takes place. Effective attraction due to ion association promotes microscopic as well as macroscopic phase separation, even under good solvent conditions for uncharged monomer units of polymer chains. Polyelectrolyte-type behavior at low Φ and ionomer-type behavior at high Φ result in the presence of two critical points on the phase diagrams of polyelectrolyte solutions as well as two separate regions of possible microscopic structuring. Our predictions on the new type of microphase separation are supported by experimental data on polymer solutions, membranes and gels.

We report on light sensitive microgel particles that can change their volume reversibly in response to illumination with light of different wavelengths. To make the anionic microgels photosensitive we add surfactants with a positively charged polyamine head group and an azobenzene containing tail. Upon illumination, azobenzene undergoes a reversible photo-isomerization reaction from a trans- to a cis-state accompanied by a change in the hydrophobicity of the surfactant. Depending on the isomerization state, the surfactant molecules are either accommodated within the microgel (trans- state) resulting in its shrinkage or desorbed back into water (cis-isomer) letting the microgel swell. We have studied three surfactants differing in the number of amino groups, so that the number of charges of the surfactant head varies between 1 and 3. We have found experimentally and theoretically that the surfactant concentration needed for microgel compaction increases with decreasing number of charges of the head group. Utilization of polyamine azobenzene containing surfactants for the light triggered remote control of the microgel size opens up a possibility for applications of light responsive microgels as drug carriers in biology and medicine.

The conformational behavior of an isolated semiflexible dipolar chain has been studied by molecular dynamics simulations. The dipolar chain was modeled as a backbone chain of charged beads, each containing an oppositely charged unit connected to it by a rigid spring. The main focus was on the effect of the backbone chain rigidity and the size of the charged groups on the morphology of the collapsed states of the chain formed in low-polar media where the electrostatic interactions are essential. It has been found that the stable globular conformations of the long chain of N = 256 backbone beads are a toroid and an elliptical globule. The macroscopic parameters (such as the radius of gyration and shape factors) as well as the local characteristics of these conformations (radial density distributions of ions, orientational correlations of chain segments, dipoles etc.) are studied depending on the chain stiffness. The regions of stability of a torus and an elliptical globule are found for the dipolar chains with variable dipole length and stiffness, which depend on the strength of electrostatic interactions. It has been shown that a size asymmetry of oppositely charged beads destabilizes globular states favoring elongated chain conformations. A coexistence of various metastable states was demonstrated for shorter chains of N = 128, 64, and 32.

The magnetodielectric response of magnetoactive elastomers (MAEs) in its dependence on filler concentration, magnetic field, and test frequency is studied experimentally. MAEs are synthesized on the basis of a silicone matrix filled with spherical carbonyl iron particles characterized by a mean diameter of 4.5 &micro, m. The concentration of the magnetic filler within composite materials is equal to 70, 75, and 80 mass%. The effective lossless permittivity &epsilon, &prime, as well as the dielectric loss tan&delta, grow significantly when the magnetic field increases. The permittivity increases and the dielectric loss decreases with increasing filler concentration. In the measurement frequency range between 1 kHz and 200 kHz, the frequency hardly affects the values of &epsilon, and tan&delta, in the absence of a magnetic field. However, both parameters decrease considerably with the growing frequency in a constant magnetic field. The more strongly the magnetic field is applied, the larger the change in permittivity and loss tangent at the same test frequency is observed. An equivalent circuit formulation qualitatively describes the main tendencies of the magnetodielectric response.

A joint theoretical and experimental study is devoted to the swelling and electrical conductivity of highly charged polyelectrolyte (PE) gels in media of different polarity. Deprotected poly(tert-butyl carbamate l-alanine) gels provided with fluorine, bromine, chlorine, sulfate, and trifluoroacetic counteranions demonstrated different conductivity in aqueous medium as well as solvent uptake in water/methanol mixtures. Counterion specificity in PE gel properties was theoretically explained in the framework of the model which treats ion association within the network as a two-stage process. Manning-type condensation, being the first condensation stage not affected by counterion type, provides understanding of a gel maximal swelling at intermediate degrees of gel ionization f and a slight gel contraction at f tending to unity, which were earlier observed in experimental investigations. The second ion association stage is an ion pairing influenced by the kind of counterion. Since a considerable fraction of io...

A comparative analysis of intramolecular dynamics of four types of isolated dendrimers from the fourth to the seventh generations belonging to the siloxane and carbosilane families, differing in spacer length, core functionality, and the type of chemical bonds, has been performed via atomic molecular dynamics simulations. The average radial and angular positions of all Si branching atoms of various topological layers within the dendrimer interior, as well as their variations, have been calculated, and the distributions of the relaxation times of their radial and angular motions have been found. It has been shown that the dendrons of all the dendrimers elongate from the center and decrease in a solid angle with an increasing generation number. The characteristic relaxation times of both angular and radial motions of Si atoms are of the order of a few nanoseconds, and they increase with an increasing generation number and decrease with temperature, with the angular relaxation times being larger than the radial ones. The relaxation times in the carbosilanes are larger than those in the siloxanes. The rotational angle dynamics of the carbosilane dendrimers show that the chain bending is mainly realized via trans-gauche transitions in the Si branching bonds.

Conformational behavior of a single strongly charged polyelectrolyte chain in a dilute solution is studied by molecular dynamics simulations. The novel feature of the model is variation of the excluded volume of counterions for investigating its effect on the chain conformation, especially in low-polar media. It has been confirmed that the chain with conventional counterions collapses into a dense globule with increasing electrostatic interactions. However, if the counterions are bulky enough, they prevent the chain collapse even in media with strong electrostatic interactions. They stay bound in the vicinity of the backbone of the chain that adopts a swollen conformation. In this conformation, the scaling relation for the polymer dimensions with the chain length is the same as for neutral macromolecules in a good solvent, however the polyelectrolyte chain complexed with bulky counterions has a larger gyration radius than its uncharged analogue due to the excluded volume of the counterions contributing to the chain rigidity. Study of the counterion mobility has shown that, similar to the conventional counterions, the bulky counterions do not form stable ion pairs with ions on the polymer chain even in media with strong electrostatic interactions, but rather freely move along the chain backbone. In solutions containing mixtures of counterions with a bimodal size distribution, the conformations of linear polyelectrolytes depend considerably on the fraction of bulky counterions. Furthermore, a kind of intramolecular microphase separation can take place within a polyelectrolyte globule with the formation of a core-shell particle: the smaller counterions concentrate within the globular core while the bulkier counterions form a shell on the globule surface. The stability of the core-shell globule depends on the relative size of the counterions as well as their fractions in the solution. Thus, fine tuning of the balance between the counterion excluded volume and the electrostatic interactions opens new ways for controlling the conformational behavior of polyelectrolytes.

This chapter introduces composite smart materials known as magnetoactive (MAEs) or magnetorheological elastomers. It starts by defining these materials and distinguishing them from relevant magnetorheological fluids and ferrofluids. It then gives the overview of constitutive materials for the polymer matrix and filler particles. Next, the influence of external magnetic field on physical properties of MAEs is discussed. The emphasis is made on mechanical properties, which are the most important for real-world applications. In particular, magnetomechanical effects such as magnetostriction, magnetodeformation, and magnetorheological effect are discussed. The magnetic Payne effect is presented as an example of a nonlinear behavior. Electromagnetic and acoustic properties are also considered. The chapter finishes with the brief discussion of the future prospects in research and development of MAEs.

The dynamic shear modulus of magnetoactive elastomers containing 70 and 80 mass % of carbonyl iron microparticles is measured as a function of strain amplitude via dynamic torsion oscillations in various magnetic fields. The results are presented in terms of the mechanical energy density and considered in the framework of the conventional Kraus model. The form exponent of the Kraus model is further related to a physical model of Huber et al. [Huber et al., J. Phys.: Condens. Matter 8, 409 (1996)] that uses a realistic representation for the cluster network possessing fractal structure. Two mechanical loading regimes are identified. At small strain amplitudes the exponent \ensuremath{\beta} of the Kraus model changes in an externally applied magnetic field due to rearrangement of ferromagnetic-filler particles, while at large strain amplitudes, the exponent \ensuremath{\beta} seems to be independent of the magnetic field. The critical mechanical energy characterizing the transition between these two regimes grows with the increasing magnetic field. Similarities between agglomeration and deagglomeration of magnetic filler under simultaneously applied magnetic field and mechanical shear and the concept of jamming transition are discussed. It is proposed that the magnetic field should be considered as an additional parameter to the jamming phase diagram of rubbers filled with magnetic particles.

Magneto-active elastomers (MAEs) based on a silicon polymer matrix filled with magnetic carbonyl iron microparticles have been synthesized. Both isotropic samples and samples micro-structured by an external magnetic field have been obtained. The radio-absorbing properties of the MAEs have experimentally been studied in the frequency range 2–10 GHz and at the central work frequency 30 GHz of the range 26–38 GHz in the absence and in the presence of an external magnetic field of 0.3 T. It has been shown that both the reflection and transmission coefficients of the MAEs change considerably when the magnetic field is applied, besides, their values strongly depend on the direction of the magnetic field as well as on the internal filler structure of MAEs. The developed MAEs could be used as controllable by an external magnetic field radio-shielding or polarizing covers.

Conformational behaviour of hydrophobically modified (HM) polymer gels in solutions of nonionic surfactants is studied theoretically. A HM gel contains hydrophobic side chains (stickers) grafted to its subchains. Hydrophobic stickers are capable to aggregate into joint micelles with surfactant molecules. Micelles containing more than one sticker serve as additional physical cross-links of the network, and their formation causes gel shrinking. In the proposed theoretical model, the interior of the gel/surfactant complex is treated as an array of densely packed spherical polymer brushes consisting of gel subchains tethered to the surface of the spherical sticker/surfactant micelles. Effect of stickers length and grafting density, surfactant concentration and hydrophobicity on gel swelling as well as on hydrophobic association inside it is analyzed. It is shown that increasing surfactant concentration can result in a gel collapse, which is caused by surfactant-induced hydrophobic aggregation of stickers, and a successive gel reswelling. The latter should be attributed to a growing fraction of surfactants in joint aggregates and, hence, increasing number of micelles containing only one sticker and not participating in gel physical cross-linking. In polyelectrolyte (PE) gels hydrophobic aggregation is opposed by osmotic pressure of mobile counterions, so that at some critical ionization degree hydrophobic association is completely suppressed. Hydrophobic modification of polymers is shown to open new ways for controlling gel responsiveness. In particular, it is discussed that incorporation of photosensitive groups into gel subchains and/or surfactant tail could give a possibility to vary the gel volume by light. Since hydrophobic aggregation regularities in gels and solutions are common, we hope our findings will be useful for design of polymer based self-healing materials as well.

New composite materials consisting of polymer matrix with PZT and NdFeB microparticles were prepared and investigated in the work. It was found that magnetic properties such as saturation magnetization, coercivity, permeability, depend on mass concentration of the ferromagnetic particles in the samples. Also it was found that all samples had electrical polarization in DC external electric field. The electric properties such as coercivity, remanent polarization, the maximum polarization value, had changes in the external constant magnetic field 1.1 kOe. These changes depended on both concentrations of ferromagnetic and ferroelectric particles. This type of magnetoelectric transformation allows us to classify new materials as multiferroic materials. These new composite materials can easily be prepared of any shape, the final materials are flexible and resistant to external chemical influences. The area of application of new multiferroic materials varies from sensors to autonomous energy sources.