The influence of the addition of ionic liquids on the properties of rubber-coated fabrics filled with layered fillers

Oceniono wpływ dodatku do mieszanek kauczukowych cieczy jonowych – bromku oraz chlorku 1-butylo-3-metyloimidazoliowego – na właściwości kompozytów tkaninowo-gumowych. Kompozyty otrzymywano na bazie tkaniny poliamidowej, którą pokrywano cienką warstwą wulkanizatu kauczuków butylowego lub butadienowo-akrylonitrylowego, napełnionych talkiem bądź miką. Dodatek napełniaczy modyfikowanych cieczami jonowymi w istotnym stopniu powodował zmniejszenie palności badanych materiałów, z zachowaniem adhezji wulkanizatu do tkaniny poliamidowej oraz ich właściwości mechanicznych, nawet po procesie starzenia termicznego.The effect of ionic liquid additives,1-butyl-3-metyloimidazolium bromide and chloride, on the properties of rubber-textile composites was examined. The composites were obtained from polyamide fabric covered with a thin layer of vulcanizate (butyl rubber or acrylonitrile-butadiene rubber) and filled with talc or mica. The addition of fillers modified with ionic liquids significantly reduced flammability of the investigated materials, without deterioration of their mechanical properties and adhesion between vulcanizate and polyamide fabric, even after thermal aging process

The Influence of Various Photoinitiators on the Properties of Commercial Dental Composites

The aim of this article was to compare the biomechanical properties of commercial composites containing different photoinitiators: Filtek Ultimate (3M ESPE) containing camphorquinone (CQ); Estelite Σ Quick (Tokuyama Dental) with CQ in RAP Technology®; Tetric EvoCeram Bleach BLXL (Ivoclar Vivadent AG) with CQ and Lucirin TPO; and Tetric Evoceram Powerfill IVB (Ivoclar Vivadent AG) with CQ and Ivocerin TPO. All samples were cured with a polywave Valo Lamp (Ultradent Products Inc.) with 1450 mW/cm2. The microhardness, hardness by Vicker’s method, diametral tensile strength, flexural strength and contraction stress with photoelastic analysis were tested. The highest hardness and microhardness were observed for Filtek Ultimate (93.82 ± 17.44 HV), but other composites also displayed sufficient values (from 52 ± 3.92 to 58,82 ± 7.33 HV). Filtek Ultimate not only demonstrated the highest DTS (48.03 ± 5.97 MPa) and FS (87.32 ± 19.03 MPa) but also the highest contraction stress (13.7 ± 0.4 MPa) during polymerization. The TetricEvoCeram Powerfill has optimal microhardness (54.27 ± 4.1 HV), DTS (32.5 ± 5.29 MPa) and FS (79.3 ± 14.37 MPa) and the lowest contraction stress (7.4 ± 1 MPa) during photopolymerization. To summarize, Filtek Ultimate demonstrated the highest microhardness, FS and DTS values; however, composites with additional photoinitiators such as Lucirin TPO and Ivocerin have the lowest polymerization shrinkage. These composites also have higher FS and DTS and microhardness than material containing CQ in Rap Technology

Can TPO as Photoinitiator Replace “Golden Mean” Camphorquinone and Tertiary Amines in Dental Composites? Testing Experimental Composites Containing Different Concentration of Diphenyl(2,4,6-trimethylbenzoyl)phosphine Oxide

The aim of this research was to compare the biomechanical properties of experimental composites containing a classic photoinitiating system (camphorquinone and 2-(dimethylami-no)ethyl methacrylate) or diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) as a photoinitiator. The produced light-cured composites consisted of an organic matrix-Bis-GMA (60 wt.%), TEGDMA (40 wt.%) and silanized silica filler (45 wt.%). Composites contained 0.27; 0.5; 0.75 or 1 wt.% TPO. Vickers hardness, microhardness (in the nanoindentation test), diametral tensile strength, resistance to three-point bending and the CIE L* a* b* colorimetric analysis was performed with each composite produced. The highest average Vickers hardness values were obtained for the composite containing 1 wt.% TPO (43.18 ± 1.7HV). The diametral tensile strength remains on regardless of the type and amount of photoinitiator statistically the same level, except for the composite containing 0.5 wt.% TPO for which DTS = 22.70 ± 4.7 MPa and is the lowest recorded value. The highest average diametral tensile strength was obtained for the composite containing 0.75 wt.% TPO (29.73 ± 4.8 MPa). The highest modulus of elasticity characterized the composite containing 0.75 wt.% TPO (5383.33 ± 1067.1 MPa). Composite containing 0.75 wt.% TPO has optimal results in terms of Vickers hardness, diametral tensile strength, flexural strength and modulus of elasticity. Moreover, these results are better than the parameters characterizing the composite containing the CQ/DMAEMA system. In terms of an aesthetic composite containing 0.75 wt.%. TPO is less yellow in color than the composite containing CQ/DMAEMA. This conclusion was objectively confirmed by test CIE L* a* b*

Enhanced Hydrophobicity of Polymers for Protective Gloves Achieved by Geometric, Chemical and Plasma—Surface Modification

Gloves are one of the most important elements of personal protective equipment (PPE). To improve gloves properties, a lot of different methods of surface modifications are used. In this work, the application of geometric, chemical, and plasma surface modifications to improve the hydrophobicity of butyl (IIR) and silicone (MVQ) rubber are described. To characterise surface properties contact angle measurements, FT-IR spectroscopy and scanning electron microscopy were used. This study showed that when the chemical modification applied, the contact angle value increases compared to non-modified samples. In addition, plasma modification raised the contact angle value and smoothed the surface morphology. An increase in the polymer surfaces hydrophobicity was the observed effect of the three modifications of rubber

SBR Vulcanizates Filled with Modified Ground Tire Rubber

Ground tire rubber (GTR) is used to decrease the cost of vulcanizates. However, insufficient interactions between GTR particles and rubber matrices make mechanical properties of vulcanizates containing GTR deteriorate. This paper compares original methods of GTR modification. The effects of surface activation of GTR by sulfuric acid (A), its modification by (3-mercaptopropyl)trimethoxy silane (M), or the hybrid treatment—combining both approaches (H), were analyzed in terms of surface energy, specific surface area and morphology of GTR particles. Vulcanizates containing virgin GTR were compared to the rubber filled with the modified GTR particles keeping the same amount of CB in the rubber mix, according to their crosslink density, mechanical and tribological properties. Contrary to the virgin GTR, the addition of modified GTR increases the stiffness of the vulcanizates. The highest changes have been observed for the samples filled with ca. 12 phr of the GTR modified with silane and ca. 25 phr of the GTR subjected to the hybrid treatment, representing the highest crosslink density of rubber vulcanizates filled with GTR. Furthermore, the addition of modified GTR, especially in the case of the samples where 10 phr of rubber was replaced, results in the significant lowering of friction but higher abrasive wear

Bitumen Binders Modified with Sulfur/Organic Copolymers

With the continuing growth of waste sulfur production from the petroleum industry processes, its utilization for the production of useful, low-cost, and environmentally beneficial materials is of primary interest. Elemental sulfur has a significant and established history in the modification of bitumen binders, while the sulfur-containing high-molecular compounds are limited in this field. Herein, we report a novel possibility to utilize the sulfur/organic copolymers obtained via the inverse vulcanization process as modifiers for bitumen binders. Synthesis and thermal characterization (TGA-DSC) of polysulfides derived from elemental sulfur (S8) and unsaturated organic species (dicyclopentadiene, styrene, and limonene) have been carried out. The performance of modified bitumen binders has been studied by several mechanical measurements (softening point, ductility, penetration at 25 °C, frass breaking point, adhesion to glass and gravel) and compared to the unmodified bitumen from the perspective of normalized requirements concerning polymer-modified bitumen. The interaction of bitumen binder with sulfur/organic modifier has been studied by means of FTIR spectroscopy and DSC measurements. The impact of the modification on the performance properties of bitumen has been demonstrated. The bitumen binders modified with sulfur/organic copolymers are in general less sensitive to higher temperatures (higher softening point up to 7 °C), more resistant to permanent deformations (lower penetration depth), and more resistant to aging processes without intrusive deterioration of parameters at lower temperatures. What is more, the modification resulted in significantly higher adhesion of bitumen binders to both glass (from 25% up to 87%) and gravel surfaces in combination with a lower tendency to form permanent deformations (more elastic behavior of the modified materials)

Fly Ash from Lignite Combustion as a Filler for Rubber Mixes—Part II: Chemical Valorisation of Fly Ash

Fly ash (FA) fractions with a particle size of 63 µm < FA < 250 µm obtained by sieve fractionation were used as a partial carbon black (CB) replacement in a rubber mixture based on styrene-butadiene rubber (SBR). In order to improve the interactions at the interface between rubber and fractionated ash, at the stage of preparing the rubber mixtures, two different vinyl silanes were added to the system: Vinyltrimethoxysilane (U-611) or Vinyl-tris (2-methoxy-ethoxy) silane (LUVOMAXX VTMOEO DL50), silane with epoxy groups: 3-(glycidoxypropyl)trimethoxysilane (U-50) or sulfur functionalized silanes: containing sulfide bridges: Bis(triethoxysilylpropyl)polysulfide silane (Si-266) or mercapto groups: Mercaptopropyltrimethoxysilane (Dynaslan MTMO). The conducted research confirmed the effectiveness of silanization with selected functional silanes, from the point of view of improving the processing and operational properties of vulcanizates, in which CB is partially replaced with the finest fractions of fly ash. The silanization generally increased the interaction at the rubber–ash interface, while improving the degree of filler dispersion in the rubber mixture. The results of TGA and FTIR analyses confirmed the presence of silanes chemically bonded to the surface of fly ash particles. SEM tests and determination of the bound rubber (BdR) content show that the introduction of the silanes to the mixture increases the degree of ash dispersion (DI) and the Payne effect, which is the greatest when mercaptosilane was used for modification. The highest increase in torque, which was recorded in the case of rubber mixtures containing sulfur silanes and silane with epoxy groups, may be due to their participation in the vulcanization process, which is confirmed by the results of vulcametric studies. The lowest values of mechanical strength, elongation at break, and the highest hardness of vulcanizates obtained in this case may be the result of the over-crosslinking of the rubber. The addition of sulfur-containing silanes significantly slowed down the vulcanization process, which is particularly visible (up to three times extension of the t90 parameter, compared to mixtures without silane) in the case of Si-266. The addition of silanes, except for Si-266 (with a polysulfide fragment), generally improved the abrasion resistance of vulcanizates. The Dynaslan MTMO silane (with mercapto groups) performs best in this respect. Proper selection of silane for the finest fraction of fly ash in the rubber mixtures tested allows for an increase in the mechanical strength of their vulcanizates from 9.1 to 17 MPa, elongation at break from 290 to 500%, hardness from 68 to 74 °ShA, and reduction in abrasion from 171 to 147 mm3

Thermal Stability and Flammability of Styrene-Butadiene Rubber-Based (SBR) Ceramifiable Composites

Ceramifiable styrene-butadiene (SBR)-based composites containing low-softening-point-temperature glassy frit promoting ceramification, precipitated silica, one of four thermally stable refractory fillers (halloysite, calcined kaolin, mica or wollastonite) and a sulfur-based curing system were prepared. Kinetics of vulcanization and basic mechanical properties were analyzed and added as Supplementary Materials. Combustibility of the composites was measured by means of cone calorimetry. Their thermal properties were analyzed by means of thermogravimetry and specific heat capacity determination. Activation energy of thermal decomposition was calculated using the Flynn-Wall-Ozawa method. Finally, compression strength of the composites after ceramification was measured and their micromorphology was studied by scanning electron microscopy. The addition of a ceramification-facilitating system resulted in the lowering of combustibility and significant improvement of the thermal stability of the composites. Moreover, the compression strength of the mineral structure formed after ceramification is considerably high. The most promising refractory fillers for SBR-based ceramifiable composites are mica and halloysite