Effect of surface cationization on the conformal deposition of polyelectrolytes over cotton fibers

The effect of surface cationization on the conformal deposition of alternating nanolayers of poly(sodium styrene sulfonate) (PSS) [Kleinfeld E, Ferguson G (1996) Chem Mater 8:1575–1578] and poly(allylamine hydrochloride) (PAH) over cotton fibers is reported. Three different levels of cotton cationization were evaluated. Variations in the cationization degree were achieved by manipulating the ratio of 3-chloro-2-hydroxy propyl trimethyl ammonium to NaOH. Experimental results obtained via Carbon–Hydrogen–Nitrogen–Sulfur (CHNS) elemental analysis and X-ray Photoelectron Spectroscopy (XPS) indicated that the deposition process was not significantly influenced by the degree of cotton cationization. The build up of further polyelectrolyte layers was found to be less sensitive to variations in the cationic character of the substrates once a critical number of alternating layers was deposited.     

Hydrophobically modified polyelectrolytes I. Dilute solution properties of fluorocarbon-containing poly (acrylic acid)

Dilute solution viscosity of fluorocarbon‐containing hydrophobically modified poly (acrylic add) was measured in aqueous solutions of various NaCl concentrations. The intrinsic viscosity ([η]) and Huggins coefficient (k_H) were evaluated using Huggins equations. It is found that, at low Nacl concentration, the modified polymers exhibit values of intrinsic viscosity ([η]) and Huggins coefficient (k_H) similar to those of unmodified polymers. For both of the modified and unmodified polymers, the intrinsic viscosity decreases with increase of NaCl concentration, while the Huggins coefficient increases upon addition of NaCl. But the variation of [η] and k_H is more significant for the modified polymers, which reflects the enhanced intra‐ and intermolecular hydrophobic association at higher Nacl concentration.     

Dislocation-mediated strain hardening in tungsten: Thermo-mechanical plasticity theory and experimental validation

A self-consistent thermo-mechanical model to study the strain-hardening behavior of polycrystalline tungsten was developed and validated by a dedicated experimental route. Dislocation–dislocation multiplication and storage, as well dislocation-grain boundary (GB) pinning were the major mechanisms underlying the evolution of plastic deformation, thus providing a link between the strain hardening behavior and material's microstructure. The microstructure of the polycrystalline tungsten samples has been thoroughly investigated by scanning and electron microscopy. The model was applied to compute stress–strain loading curves of commercial tungsten grades, in the as-received and as-annealed states, in the temperature range of 500–1000 °C. Fitting the model to the independent experimental results obtained using a single crystal and as-received polycrystalline tungsten, the model demonstrated its capability to predict the deformation behavior of as-annealed samples in a wide temperature range and applied strain. The relevance of the dislocation-mediated plasticity mechanisms used in the model have been validated using transmission electron microscopy examination of the samples deformed up to different amounts of strain. On the basis of the experimental validation, the limitations of the model are determined and discussed.     

Synthesis and interfacial properties of novel cationic polyelectrolytes with brush-on-brush structure of poly(ethylene oxide) side chains

Novel cationic polyelectrolytes with a brush-on-brush structure of poly(ethylene oxide) (PEO) side chains and a charge-containing polyacrylate backbone were synthesized. The PEO side chains were not directly attached to the backbone but via polymethacrylate spacers, thus locating the PEO chains a distance away from the charged units of the backbone. The cationic brush-on-brush polyelectrolytes with high density of PEO chains showed a strong affinity to silica surfaces, provided the backbone charge density was high enough. The adsorption of these polymers was studied by QCM-D giving very high sensed mass, 20 mg/m². It was shown by direct force measurements that protective surface layers were formed by the novel polyelectrolytes, generating strongly repulsive steric forces, which provided an effective barrier against flocculation. The adsorbed layer was sufficiently robust to withstand sliding experiments under a pressure of up to 35 MPa. The friction force in water was very low, and the lubrication was characterized by a friction coefficient in the range of 0.02-0.06.     

Soft magnetic properties of NiFe compacted powder alloys

It is known that Ni–Fe based alloys (permalloys) are important soft magnetic materials, which have been widely applied in the field of electronic devices and industry. The most suitable permalloys for application exhibit low value of coercivity and magnetostriction (for about 80 at% Ni), high saturation magnetic induction (for about 50 at% Ni), higher electrical resistivity (for about 35 at% Ni). The aim of this work was to investigate the structure and magnetic properties of _Ni81Fe19${\mathrm{Ni}}_{81}{\mathrm{Fe}}_{19}$ (wt%) compacted powder material in the form of small cylinders.     

Hydrogen annealing effects on polycrystalline La0.67Ba0.33MnO3 compound

Upon annealing polycrystalline La_0.67Ba_0.33MnO₃ bulk samples in flowing 95%Ar:5%H₂ mixed gas at 700 °C for different time, the insulator–metal transition temperature, _TP$T_{\mathrm{P}}$ and the amplitude of AC magnetic susceptibility were decreased first, then increased, finally decreased again. While the resistivity was increased monotonically. This anomalous behavior was explained by the combinational effects of oxygen loss and Ba ion vacancies caused by the segregation of Ba ion related impurity phase.     

Zwitterionically modified hydroxypropylcellulose for biomedical applications

Novel polyelectrolytes have been synthesized by grafting sulfobetaine side chains onto hydroxypropylcellulose backbone. Polymers with various degrees of grafting have been obtained. The polymers do not interact with model anionic, cationic and zwitterionic surfactants as found in fluorescence studies using pyrene as a molecular probe. Dynamic light scattering (DLS) studies indicated that in the graft polymer solution two types of polymers are present. The films were formed from the grafted polymers. Using atomic force microscopy (AFM) technique it was found that they are resistant to the adhesion of proteins and can be used for the preparation of antiadhesive surfaces which may find biomedical applications.     

Influence of particle surface properties on the dielectric behavior of silica/epoxy nanocomposites

Silica/epoxy composites have been widely used in functional electric device applications. Silica nanoparticles, both unmodified and modified with the coupling agent KH-550, were used to prepare epoxy composites. Dielectric measurements showed that nanocomposites exhibit a higher dielectric constant than the control sample, and had more obvious dielectric relaxation characteristics. Results showed that particle surface properties have a profound effect on the dielectric behavior of the nanocomposites. These characteristics are attributed to the local ununiformity of the microstructure caused by the large interface area and the interaction between the filler and the matrix. This phenomenon is explained in terms of prolonging chemical chains created during the curing process. The mechanism is discussed with measurements of X-ray diffraction (XRD) and Fourier transform infrared (FTIR).     

Polymers containing quaternary ammonium groups based on poly(N-vinylimidazole)

A poly(N-vinylimidazole) (PNVI)—based poly(carboxybetaine) with two methylene groups between the opposite charges was achieved by the nucleophilic addition reaction of the mentioned aminic polymer to the carbon-carbon double bond of acrylic acid (AA). Treatment of poly(carboxybetaine) with concentrated HCl (2 N) for long time leads to the corresponding cationic polyelectrolyte. The poly(carboxybetaine) is soluble in both water and aqueous solutions of salts such as: LiCl, NaCl, NaHCO₃, CaCl₂, Na₂SO₄. In water and in the first three salts, poly(carboxybetaine) exhibits a non-polyelectrolyte behaviour (a linear dependence of reduced viscosities on polymer or salt concentration), while in the remaining two salts, a slight polyelectrolyte behaviour is observed. The cationic polyelectrolyte is soluble in water and aqueous solutions of LiCl, NaCl, CaCl₂ and NaHCO₃, except Na₂SO₄. It has a polyelectrolyte behaviour in all solutions. Also, the binding trends of the added salts by polymers are discussed.     

Electronic structure and ferromagnetism of polycrystalline Zn1−xCoxO (0≤x≤0.15)

The electronic structure of polycrystalline ferromagnetic Zn_1−xCo_xO (0.05≤x≤0.15) and the oxidation state of Co in it, have been investigated. The Co-doped polycrystalline samples are synthesized by a combustion method and are ferromagnetic at room temperature. XPS and optical absorption studies show evidence for Co²⁺ ions in the tetrahedral symmetry, indicating substitution of Co²⁺ in the ZnO lattice. However, powder XRD and electron diffraction data show the presence of Co metal in the samples. This give evidence to the fact that some Co²⁺ ion are incorporated in the ZnO lattice which gives changes in the electronic structure whereas ferromagnetism comes from the Co metal impurities present in the samples.