Effect of Composition on the Physicochemical Properties of Cross-Linked Poly(sodium acrylate)/Sodium Silicate Hydrogels.

The paper presents the results of research on the influence of the components of composition on the physicochemical properties of cross-linked poly(sodium acrylate)/sodium silicate hydrogels. The results of the rheological measurements showed that an increasing share of polyacrylate in the sample causes a shift of the cross-over point towards longer times and improves mechanical properties. In turn, increasing the share of sodium silicate has a positive effect on extending the fire insulation time (I). TG/DSC analysis indicated that if the sample contained more than 50 wt.% of polymer, the thermal decomposition was a three-stage process, while if the sample contained more water glass, the decomposition was two stage. UV-Vis measurements and SEM analysis confirmed, inter alia, that increasing the share of polyacrylate causes improvement of the optical parameters and homogeneity of the tested hydrogels. The presented results suggest that by controlling the share of the main components of the silicate-polymer hydrogels, it is possible to control their mechanical, optical and thermal properties. Multiplication of the layers or increasing their thickness improves their fire-retardant properties.

Effect of Ionic and Non-Ionic Surfactant on Bovine Serum Albumin Encapsulation and Biological Properties of Emulsion-Electrospun Fibers.

Emulsion electrospinning is a method of modifying a fibers' surface and functional properties by encapsulation of the bioactive molecules. In our studies, bovine serum albumin (BSA) played the role of the modifier, and to protect the protein during the electrospinning process, the W/O (water-in-oil) emulsions were prepared, consisting of polymer and micelles formed from BSA and anionic (sodium dodecyl sulfate-S) or nonionic (Tween 80-T) surfactant. It was found that the micelle size distribution was strongly dependent on the nature and the amount of the surfactant, indicating that a higher concentration of the surfactant results in a higher tendency to form smaller micelles (4-9 µm for S and 8-13 µm for T). The appearance of anionic surfactant micelles reduced the diameter of the fiber (100-700 nm) and the wettability of the nonwoven surface (up to 77°) compared to un-modified PCL polymer fibers (100-900 nm and 130°). The use of a non-ionic surfactant resulted in better loading efficiency of micelles with albumin (about 90%), lower wettability of the nonwoven fabric (about 25°) and the formation of larger fibers (100-1100 nm). X-ray photoelectron spectroscopy (XPS) was used to detect the presence of the protein, and UV-Vis spectrophotometry was used to determine the loading efficiency and the nature of the release. The results showed that the location of the micelles influenced the release profiles of the protein, and the materials modified with micelles with the nonionic surfactant showed no burst release. The release kinetics was characteristic of the zero-order release model compared to anionic surfactants. The selected surfactant concentrations did not adversely affect the biological properties of fibrous substrates, such as high viability and low cytotoxicity of RAW macrophages 264.7.

The Effect of Magnesium Hydroxide Addition on the Extinguishing Efficiency of Sodium Bicarbonate Powders.

This article analyzes the possibility of the modification of BC powder (a mixture of sodium bicarbonate and calcium carbonate) with magnesium hydroxide (Mg(OH)2). Extinguishing efficiency as well as the influence of this additive on other physicochemical properties were determined by performing a 13B fire test, rheological measurements of the powders, thermal tests (thermogravimetry (TG) and differential scanning calorimetry (DSC) in combination with quadrupole mass spectrometry (QMS)) and microscopic observations of the powders' surface (scanning electron microscope (SEM) with energy dispersive X-ray analysis (EDS)). It was found that the increase of the Mg(OH)2 content causes deterioration of the rheological properties by increasing the slope angle of the flow curve in relation to the normal stress (the tangent of the flow curve slope varying from 0.258 for 5% of Mg(OH)2 up to 0.330 for 20% of Mg(OH)2). However, at the same time, the increased content of Mg(OH)2 increases the total energy of the chemical decomposition reaction (from -47.27 J/g for 5% of Mg(OH)2 up to -213.6 J/g for 20% of Mg(OH)2) resulting in the desirable higher level of heat removal from the fire. The initial extinguishing effect of the fire becomes more effective as the hydroxide content increases (within the first 2 s), but at a later stage (from t = 63 s), the temperature is no longer sufficient (it is below 350 °C) for thermal decomposition of Mg(OH)2. As such, the optimal content of Mg(OH)2 is 10-15%. The obtained results allowed for the assessment of the impact of individual powder components on its extinguishing effect and will contribute to the development of science in the field of developing new types of extinguishing powders.

Rheological Properties of Soft Waste Granulates Produced in the Fabrication Process of Ceramic Tiles and the Possibility of Their Reuse.

The paper presents the results of research on the influence of the granulometric composition on the rheological properties of granulates from soft waste produced in the manufacturing of ceramic tiles using the Lamgea and Continua methods in terms of the possibility of their reuse. The composition of the granulates was modified by removing individual grain fractions in three measurement series. Comparatively, the measurement samples for the production granulates were prepared in the same way. Microscopic observations and granulometric analysis showed significant differences in the grain shape and grain size distribution of granulates. The soft waste granulates also showed much worse flow ability than the production granulates. It was shown that the removal of the smallest fractions significantly improved the rheological properties of soft waste granulates. This tendency was also observed in the case of measurements of changes in the bulk density. A Brookfield powder analyzer was used for rheological tests, and a flow analysis was performed using the numerical Jenike classification.

The Effect of Humidity on the Atomization Process and Structure of Nanopowder Designed for Extinguishment.

Increasingly, firefighting aerosols are being used to extinguish fires. It is assumed that the extinguishing mechanism involves breaking the chain of physicochemical reactions occurring during combustion by binding free radicals at ignition. The radicals are most likely formed from the transformation of water molecules, with the active surfaces of aerosol micro- or even nanoparticles. The aerosol extinguishing method is very effective even though it does not reduce oxygen levels in the air. In contrast to typical extinguishing powders, the aerosol leaves a trace amount of pollutants and, above all, does not adversely affect the environment by depleting the ozone layer and increasing greenhouse effects. Depending on how the firefighting generators are released, the aerosol can act locally or volumetrically, but depending on environmental conditions, its effectiveness can be variable. The article presents the influence of environmental humidity on the atomization of aerosol nanosize, which confirms the radical combustion mechanism. This paper presents the effect of environmental humidity on the atomization of aerosol superfine (nano) particles. The main focus was on the grain distribution and its effect on the surface activity of the FP-40C type firefighting aerosol. Changes in the characteristic parameters of the particle size distribution of RRSB (Rosin-Rammler-Sperling-Bennet) are presented.

Fabrication of Polyurethane/Polylactide (PU/PLDL) Nanofibers Using Electrospinning Method.

Polylactide and aliphatic polyurethane are biodegradable synthetic polymers which are broadly used as biomaterials in regenerative medicine for implants and scaffolds for tissue engineering. In this paper, the detailed studies of the fabrication of the electrospun fibers of polyurethane/polylactide mixtures were described. The influence of the used solvent (dimethylformamide (DMF)) and diluents (acetone and dichloromethane (DCM)) on the rheological parameters and electrospinning of the described mixtures was examined. Rheological studies showed that polyure-thane/polylactide mixtures have mostly non-Newtonian character, strongly influenced by the diluent. Solutions containing 50 wt.% or more of polyurethane became less viscous after the addition of DCM or acetone, whereas those with bigger amount of polylactide showed higher viscosity after the addition of DCM and lower viscosity after the addition of acetone. Optimized electrospinning process has been elaborated. Fibers with diameters from 250 nm up to 1 µm have been produced and compared. Pure acetone worsened the electrospinning process, but the more DCM was in the mixture, the thinner and more aligned fibers were produced.

Research on the Thermal Properties of Fireplace Concrete Materials Containing Various Mineral Aggregates Enriched by Organic and Inorganic Fibers.

This work presents a summary of research on concrete fireplace materials made of various mineral aggregates and enriched with steel and organic fibers. To determine the optimal applications of such concretes, their ability to accumulate heat and their other physicochemical parameters were tested and analyzed. Studies on the behavior of concrete materials during cooling are reported, and the ability of such materials to accumulate heat is evaluated using calculations. In addition, tests were performed on the loss of mass during heating, as well as on the mechanical bending strength and microstructures of these materials. Studies have shown that the behavior of concrete materials at high temperatures can be modified and adapted for specific purposes. The addition of fibers to concrete improves both the mechanical properties of mortars and the heat flow in concrete materials.

Water Interactions in Hybrid Polyacrylate-Silicate Hydrogel Systems.

Hybrid polyacrylate-silicate hydrogels were obtained in the presence of N,N'-methylenebisacrylamide (NNMBA) as the cross-linking monomer and sodium thiosulphate/potassium persulphate (NTS/KPS) as the redox initiators. The results of the tests allowed us to conclude that a hybrid structure with a polyacrylate scaffolding and a silicate matrix had been obtained. The results of the rheological analysis revealed that the hydrogel sample with a 1:7 mass ratio of sodium water glass to the sodium polyacrylate is characterized by the highest complex viscosity. Thermal analysis (Thermogravimetry/Differential Scanning Calorimetry (TG/DSC)) showed that water begins to evaporate at higher temperatures, from 120 °C to even 180 °C. These results were confirmed by mid-infrared spectroscopy (MIR) and nuclear magnetic resonance spectroscopy (NMR) analysis. Differences in the intensity of the peaks derived from water in the MIR spectra indicate that most of the water is bounded. In turn, NMR results showed that the mobility of water molecules decreases as the amount of sodium water glass in the mixture increases.

Influence of the type of aqueous sodium silicate on the stabilization and rheology of kaolin clay suspensions.

To avoid agglomeration and sedimentation of grains, ceramic slurries should be modified by stabilizers in order to increase the electrostatic interactions between the dispersed particles. In this study we present the spectral analysis of aqueous sodium silicates obtained by different synthesis methods and their influence on the rheological properties of kaolin based slurries. Infrared and Raman spectra can be used to describe the structure of silicate structural units present in aqueous sodium silicates. It was confirmed that the best stabilization results possess aqueous sodium silicates of the silicate moduli of about 2 and the optimal concentration of the used fluidizer is 0.3wt% to the kaolin clay dry mass. One of the most important conclusions is that the synthesis method of the fluidizer has no significant effect on its stabilization properties but used medium does create adequate stabilization mechanism depending on the silicate structures present in the sodium silicate solution.

Biopolymeric hydrogels - nanostructured TiO2 hybrid materials as potential injectable scaffolds for bone regeneration.

The present work aims at development of novel hybrid materials from genipin crosslinked collagen or collagen/chitosan hydrogels containing various types of TiO2 nanoparticles characterized with different anatase/rutile ratios. Collagen and chitosan were selected as hydrogel components since they are biopolymers being, like collagen, the major compound present in extracellular matrix or exhibit structural similarity to glycosaminoglycans, like chitosan. TiO2 nanoparticles were introduced to the hydrogel matrices to improve their mechanical properties as well as bioactivity. A series of twelve novel hybrid materials were prepared and their physicochemical, mechanical and biological properties were evaluated. It was found that TiO2 nanostructures introduced to the hydrogels have significant influence on the swelling properties of the synthesized hybrids and their impact is strongly dependent on the type of matrices. The surfaces of hybrid materials were found to be more hydrophilic than these of corresponding hydrogel matrix. It was also observed that, the storage modulus values of the hybrids based on collagen-chitosan hydrogel are comparable to these for plain hydrogels what indicates that the mechanical properties of the materials obtained are satisfactory for possible biomedical application. The in vitro cell culture studies have shown that prepared materials are biocompatible as they can support mitochondrial activity of MEFs as well as MG-63 cells. In vitro experiments performed under simulated body fluid (SBF) conditions have revealed that all studied TiO2 nanoparticles present in hydrogel matrices, regardless of anatase/rutile ratio, successfully induced formation of apatite-like structures. The hybrid materials developed here are promising candidates for preparation of bioactive, injectable scaffolds for tissue engineering.