Study on Parameter Optimization and Mechanism of Rigid-Flexible Coupling Underground Engineering Structure of Steel Panel and Polymer

Polymer grouting is carried out between the steel panel and surrounding soil in underground engineering, and the polymer material consists of isocyanates and polyols. The isocyanate/polyol composite slurry expands rapidly due to chemical reaction and solidifies immediately. Then, a dense impermeable polymer layer is formed after rapid expansion of isocyanate and polyol, which is widely used for ground reinforcement and foundation remediation. Thus, a steel panel-polymer composite structure is developed. Mechanical properties of the steel panel-polymer structure are studied. The results show that the steel panel-polymer structure exhibited excellent mechanical properties. The steel panel and polymer layer should be designed above 3 mm and 10 mm in thickness, respectively. The steel panel showed superior mechanical properties to those of polymer layers. Considering good rigidity of the steel panel and good flexibility of the polymer layer, the steel panel and polymer layer presented perfect interfacial contact. It is concluded that the mechanical properties of the whole structure were increasingly enhanced with the increase of the steel panel thickness and the structural flexibility increased with the thickness of the polymer layer. Besides, the combination of the steel panel and polymer layer could also improve the mechanical properties of this coupling structure. This study provided an initial attempt for investigating the feasibility of applying polyurethane foam to steel panels in underground engineering. The stress analysis along the grouting direction inside the prefabricated wall was conducted. It may lay the foundation for further application of polymer grouting in underground engineering.

Model of deformation growth dynamics during filled polymer materials mechanical tests under cable production conditions

With the introduction into highly filled halogen-free plastics production, the mechanical strength of which in operation directly depends on the flame retardant content and application technology, it becomes important to control the cable sheath mechanical characteristics in a fireproof design. Polymeric materials and their compositions are viscoelastic materials for which the mechanical properties depend on the stress time. The results of estimating the deformation samples rate elongation from the uniaxial stretching time at different dilution rates of the clamps in the mechanical characteristics determining process for halogen-free cable plastics in regulatory tests under production conditions are presented. It is shown that the inner and outer layers of the halogen-free plastic cable sheath have significantly different values of the plasticity normative parameter: differences evidence in the polymer structure in the inner and outer layers of the sheath due to the forced deformation process during extrusion, which is forced polymer structure orientation. Elongation relative deformation experimental dependences δL(t) of the samples on the uniaxial stretching time at different clamps dilution speeds are given, which illustrate confirmed by a large data array the dependencies shape reproducibility δL(t) for different in structure similar filled halogen-free polymers. The strain rate dependence model on tensile time as the sum of instantaneous-elastic, viscoelastic and instantaneous-plastic (irreversible) is proposed: dε/dt = λпр exp ( – t/λпр) + {∫ λ1 exp(–τ/λ1).exp[–(t–τ)/λ2]dτ]}/Δt. The appropriate parameter estimates of the named samples deformation components obtained by approximating the experimental data by the proposed model are given. The proposed model, firstly, explains the presence characteristic relative deformation maximum (t = tm) as a two interdependent deformation processes superposition with different aftermath λ. Secondly, it allows to specify the requirements for testing: with increasing the clamps dilution speed, the maximum time tm decreases significantly, respectively, the higher the clamps dilution speed, the smaller interval time Δt between a successive sample control section length measurements. This conclusion was experimentally confirmed for a specific material at a speed of 250 mm/min

Single-variable porous nanomaterial series from polymer structure-directing agents

Block polymer structure-directing agents (SDA) enable the production of porous nanoscale materials. Most strategies rely upon polymer equilibration where diverse morphologies are realized in porous functional materials. This review details how solvent selectivity determines the polymer SDA behaviors, spanning from bulk-type to solution-type. Equilibrating behavior of either type, however, obscures nanostructure cause-and-effect since the resulting sample series convolve multiple spatial variations. Solution-type SDA behaviors include both dynamic and persistent micelles. Persistent micelle templates (PMT) use high solvent selectivity for kinetic entrapment. PMTs enable independent wall thickness control with demonstrated 2 Å precision alterations. Unimodal PMT pore size distributions have spanned from 11.8 to 109 nm and multimodal pore sizes up to 290 nm. The PMT method is simple to validate with diffraction models and is feasible in any laboratory. Finally, recent energy device publications enabled by PMT are reviewed where tailored nanomaterials provide a unique perspective to unambiguously identify nanostructure–property–performance relationships. Graphical abstract

Melanin’s Semiconductor Nature and His Polymer Structure Successfully Modifies Sulfur Cathode and Increases Efficiency on Li-S Batteries

Dynamics of change in impedance spectra and electrochemical parameters of the Li-S rechargeable batteries with non-aqueous liquid electrolyte 0.7 M LiIm, 0.25 M LiNO3, DME: DOL (2:1) during storage after assembly and cycling have been shown. For modification of the Sulfur cathode, we used the different types of melanin. Our results confirm that melanin can be used as a promising component of sulfur-based electrodes

Prolonged Thermal Relaxation of the Thermosetting Polymers

The rigidity of structures made of polymer composite materials, operated at elevated temperatures, is mainly determined by the residual rigidity of the polymer binder (which is very sensitive to elevated temperatures); therefore, the study of ways to increase the rigidity of polymer materials under heating (including prolonged heating) is relevant. In the previous research, cured thermosetting polymer structure’s non-stability, especially under heating, is determined by its supra-molecular structure domain’s conglomerate character and the high entropy of such structures. The polymer elasticity modeling proved the significance of the entropy factor and layer (EPL) model application. The prolonged heating makes it possible to release adsorptive inter-layer bonds and volatile groups. As a result, the polymer structure is changing, and inner stress relaxation occurs due to this thermo-process, called thermo-relaxation. The present study suggests researching thermo-relaxation’s influence on polymers’ deformability under load and heating. The research results prove the significant polymer structure modification due to thermo-relaxation, with the polymer entropy parameter decreasing, the glassing onset temperature point (Tg) increasing by 1.3–1.7 times, and the modulus of elasticity under heating increasing by 1.5–2 times.

Thermal and optical properties of PMMA films reinforced with Nb2O5 nanoparticles

The article presents the thermal and physical properties of PMMA composite films with the addition of Nb2O5 nanoparticles. The addition of nanoparticles to PMMA mainly influenced the optical transmission and glass transition temperature of composite films compared to pure PMMA. It is clearly visible in the results of the conducted ellipsometric and differential scanning calorimetry tests. X-ray studies showed that the heat treatment of the samples resulted in the ordering of the polymer structure (flattening of the polymer chains). Examining the surface of the samples with scanning electron microscopy, it can be seen that Nb2O5 nanoparticles formed unusual, branched formations resembling "snowflakes".