Search Results (97)

To obtain waterborne polymer-modified emulsified asphalt materials with better comprehensive performance, waterborne polymer modifiers including waterborne epoxy resin (WER)-reinforced styrene–butadiene–styrene block copolymer (SBS), waterborne acrylate (WA) or styrene butadiene rubber (SBR) emulsion were prepared. The mechanical strength, toughness, adhesion and impact resistance of these waterborne polymers were evaluated. Furthermore, the correlation between the performance indicators of the waterborne polymers was analyzed. Based on Fourier transform infrared (FTIR) spectroscopy and thermogravimetric (TG) analysis, the mechanism of WER-modified SBS and WA was characterized. The results show that adding 10%–15% WER can significantly improve the mechanical properties of the waterborne polymer. The performances of modified SBS and WA are better than that of modified SBR. When the content of WER is 10%, the tensile strength, elongation at break and pull-off strength of WER-modified SBS and WA are 4.80–6.38 MPa, 476.3%–579.6% and 1.62–1.70 MPa, respectively. The mechanical strength and breaking energy of the waterborne polymers show a significant linear correlation with their application properties such as adhesion, bonding and impact resistance. FTIR and TG analyses indicate that WER-modified SBS or WA prepared via emulsion blending undergo primarily physical modifications, enhancing thermal stability while promoting crosslinking and curing. Full article

The viscoelastic behavior of asphalt mixtures is a crucial consideration in the analysis of pavement mechanical responses and structural design. This study aims to elucidate the molecular structure and component evolution trends of polyphosphoric acid (PPA)/styrene butadiene styrene block copolymer (SBS)/styrene butadiene rubber copolymer (SBR) composite modified asphalt (CMA) under rolling thin film oven test (RTFOT) and pressure aging (PAV) conditions, as well as to analyze the viscoelastic evolution of CMA mixtures. First, accelerated aging was conducted in the laboratory through RTFOT, along with PAV tests for 20 h and 40 h. Next, the microscopic characteristics of the binder at different aging stages were explored using Fourier-transform infrared spectroscopy (FTIR) and gel permeation chromatography (GPC) tests. Additionally, fundamental rheological properties and temperature sweep tests were performed to reveal the viscoelastic evolution characteristics of CMA. Ultimately, the viscoelastic properties of CMA mixtures under dynamic loading at different aging stages were clarified. The results indicate that the incorporation of SBS and SBR increased the levels of carbonyl and sulfoxide factors while decreasing the level of long-chain factors, which slowed down the rate of change of large molecule content and reduced the rate of change of LMS by more than 6%, with the rate of change of overall molecular weight distribution narrowing to below 50%. The simultaneous incorporation of SBS and SBR into CMA mixtures enhanced the dynamic modulus in the 25 Hz and −10 °C range by 24.3% (AC-13), 15.4% (AC-16), and reduced the $\phi$ by 55.8% (AC-13), 40% (AC-16). This research provides a reference for the application of CMA mixtures in the repair of pavement pothole damage. Full article

The high- and low-temperature performance of asphalt-based seamless expansion joints seriously affects road performance. The purpose of this paper is to explore the application of thermosetting epoxy asphalt-based materials in bridge expansion joints. The composite modification of asphalt was performed using Styrene–Butadiene rubber (SBR) and Styrene–Butadiene–Styrene (SBS) copolymer. The study then investigates the impact of five different dosages of SBR/SBS-modified asphalt on the performance of epoxy asphalt. The results of the cone penetration test, tensile test, and stress relaxation test of SBR/SBS-modified epoxy asphalt (SSEA) and BJ200 (a commercial Seamless expansion joint material) were comparatively analyzed. The Marshall test, rutting test, three-point bending test, and freeze–thaw split test were used to evaluate the road performance of SSEA mixtures. The test results show that with the increase in asphalt content, the shear resistance and tensile strength of SSEA decrease, and the low-temperature relaxation ability and elongation at break increase. The content of SBR/SBS-modified asphalt has a positive effect on the low-temperature performance of SSEA mixtures, and the residual stability in water and freeze–thaw splitting strength ratio (TSR) are higher than that of BJ200. Based on the requirement of balancing high and low-temperature performance, SSEA-3 has the best overall performance, and the dosage of SBR and SBS modifier is 12% and 2.5%, respectively. The ratio of epoxy resin, SBR/SBS-modified asphalt, and the curing agent is 1:4:1.6, and its use is recommended in areas with slight temperature differences. Full article

Styrene–butadiene–styrene (SBS)-modified asphalt is widely used in the field of road construction because it helps asphalt pavements achieve good road performance. However, SBS-modified asphalt has problems of poor compatibility, leading to insufficient thermal storage stability. As a block copolymer of styrene and butadiene, the compatibility of SBS with asphalt is also influenced by its styrene-to-butadiene (S/B) ratios. To reveal the compatibility mechanisms of different S/B ratios of SBS and asphalt during system stabilization, the interactions of SBS with asphalt at the molecular level were investigated in this study. Based on the molecular dynamics simulation method, interfacial models of SBS and asphalt were constructed; the miscible process of SBS in asphalt was simulated, with the characteristics of phase structure evolution and molecular distribution being analyzed; and the binding energy of the SBS/asphalt miscible systems was calculated. The results show that a higher butadiene content benefits the miscibility of SBS in asphalt and that the S/B ratios affect the interaction of SBS with asphalt and its components. SBS with a 3:7 ratio of styrene to butadiene exhibits stronger adsorption with the resin component and has the highest binding energy and best compatibility with asphalt. The findings contribute to the understanding of the miscibility and compatibility mechanisms between different S/B ratios of SBS and asphalt. Full article

To investigate the feasibility of composite modification techniques in improving the performance of recycled asphalt mixtures, in this study, the high-viscosity agent (HVA) and crumb-rubber materials (CRM) were used to modify asphalt with a styrene-butadiene-styrene block copolymer (SBS), in order to prepare SBS-HVA and SBS-CRM composite-modified asphalts. The virgin asphalt mixtures, as well as three asphalt types of recycled asphalt mixtures with 50% reclaimed asphalt pavement (RAP) content, were designed. The optimal asphalt content of the four types of asphalt mixtures was analyzed, and the rutting test, the asphalt bond strength test, the moisture-induced sensitivity test, and the low-temperature cracking resistance test were conducted to investigate the performance of the four types of asphalt mixtures. The results showed that the higher the asphalt kinematic viscosity, the higher the optimum asphalt content of the asphalt mixtures under the same air voids. HVA significantly improves the adhesion between SBS-modified asphalt and aggregate under dry conditions, while SBS-CRM composite-modified asphalt performs similarly to SBS-modified asphalt. Before and after water immersion, the degree of pull-out strength decay between the asphalts and aggregates follows the sequence of SBS-CRM- > SBS- > SBS-HVA-modified asphalts. Additionally, the residual pull-out work follows the sequence of SBS-HVA- > SBS-CRM- > SBS-modified asphalt. SBS-CRM composite-modified asphalt can significantly improve the moisture sensitivity of recycled asphalt mixtures, as well as low-temperature cracking resistance, while SBS-CRM composite-modified asphalt only improves the low-temperature cracking resistance of recycled asphalt mixtures, and does not improve the moisture sensitivity. Based on the results, it is recommended to select the appropriate composite modification method based on the climate and loading conditions, to maximize the value of asphalt, and to achieve sustainable and durable pavement. Full article

The polymer blends are an effective strategy for materials design with new properties in the plastic industry; such features may depend on the blend components and the processing method. This study aimed to understand the effect of styrene-butadiene-styrene (SBS) content and its architecture on blends based on polyphenylene ether (PPE), high-impact polystyrene (HIPS), and SBS. In addition, this research compared and analyzed the blends formulated by different processing methods: twin-screw extrusion (TSE) and internal mixing (IM). Furthermore, three SBS copolymers, two radial and one linear (with different molecular weights), were used to produce PPE/HIPS/SBS blends, analyzing which SBS copolymer feature provides excellent viscoelasticity, thermomechanical properties, and impact resistance. The findings revealed that the melt processing method played a crucial role in Izod impact resistance of the PPE/HIPS/SBS blends, as well as the molecular architecture, molecular weight, and SBS content. The findings also demonstrated that the TSE process is more effective than the IM. Since the PPE/HIPS/SBS blends displayed higher Izod impact resistance than the PPE/HIPS or PPE/SBS binary blends, a synergistic effect of SBS and HIPS is suggested. Full article

Moisture accelerates the degradation of asphalt properties, significantly impacting the service life of roads. Therefore, this study uses simplified viscoelastic continuous damage theory and employs frequency scanning, linear amplitude scanning, and fatigue–healing–fatigue tests with a dynamic shear rheometer. The objective is to investigate the effects of aging time, moisture conditions, and aging temperature on the fatigue and self-healing performance of SBS (Styrene–Butadiene–Styrene block copolymer)-modified asphalt, nano-SiO₂-modified asphalt, and nano-SiO₂/SBS composite modified asphalt in a moisture-rich environment. The results indicate that nano-SiO₂ powder enhances the low-temperature performance of modified asphalt, whereas the SBS modifier reduces temperature sensitivity and increases the recovery percentage after deformation. Compared to SBS-modified asphalt, the deformation resistance of nano-SiO₂/SBS composite modified asphalt has increased by about 30%, while nano-SiO₂-modified asphalt shows relatively poor deformation resistance. The fatigue performance of SBS-modified asphalt deteriorates under moisture, whereas the addition of nano-SiO₂ powder improves its fatigue life. Nano-SiO₂/SBS composite modified asphalt exhibits strong self-healing capabilities. Although self-healing can enhance the fatigue life of modified asphalt, moisture inhibits this improvement after self-healing. Full article

The regeneration performance of an aged styrene–butadiene–styrene block copolymer (SBS) will be significantly influenced by different rejuvenators. The objective of this study was to comparatively investigate the regeneration effect of different SBS-modified asphalt regenerators on aged SBS-modified asphalt. Four types of different regenerant formulations were selected. The optimal rejuvenator content was determined firstly using conventional performance tests. The rheological properties of the aged SBS-modified asphalt binder were evaluated by multiple stress creep recovery (MSCR) experiments. Subsequently, the regeneration mechanism of the SBS-modified asphalt binder was investigated using thin-layer chromatography–flame ionization detection (TLC-FID) and Fourier transform infrared spectroscopy (FTIR). The results showed that the rejuvenator had a certain recovery effect on the penetration, softening point, and ductility of the SBS-modified asphalt binder after aging. The SBS-modified rejuvenating agent was the most favorable among the four types of rejuvenators, where a rejuvenator dosage of 12% showed the optimal rejuvenation effect. The addition of regenerators could appropriately improve the elastic deformation capacity of the aged asphalt binder. The epoxy soybean oil in the regenerant reacted with the aging SBS-modified asphalt binder, supplementing the lost oil in the aged SBS-modified asphalt binder, dispersing the excessive accumulation of asphaltene, and making the residual SBS swell again. The viscoelastic properties of the aging asphalt binder were improved by adjusting the content of components and functional groups to achieve the purpose of regeneration. Full article

To promote the application of economical and sustainable polyphosphoric acid (PPA)-modified asphalt in road engineering, styrene-butadiene block copolymer (SBS), styrene-butadiene rubber (SBR), and PPA were used to prepare PPA/SBS and PPA/SBR composite-modified asphalts, which were tested and the data analyzed. Fourier transform infrared spectroscopy (FTIR) tests and thermogravimetric analysis (TG) tests were carried out to study the modification mechanisms of the composite-modified asphalts, and the high-temperature performance of the PPA-modified asphalt and asphalt mixtures was analyzed by dynamic shear rheology (DSR) tests and wheel tracking tests. A gray correlation analysis and a back-propagation (BP) neural network were utilized to construct a prediction model of the high-temperature performance of the asphalt and asphalt mixtures. The test results indicate that PPA chemically interacts with the base asphalt and physically integrates with SBS and SBR. The PPA-modified asphalt has a higher decomposition temperature than the base asphalt, indicating superior thermal stability. As the PPA dosage increases, the G*/sinδ value of the PPA-modified asphalt also increases. In particular, when 0.6% PPA is combined with 2% SBS/SBR, it surpasses the high-temperature performance achieved with 4% SBS/SBR, suggesting that PPA may be a good alternative for polymer modifiers. In addition, the creep recovery of PPA-modified asphalt is influenced by the stress level, and as the stress increases, the R-value decreases, resulting in reduced elastic deformation. Furthermore, the BP neural network model achieved a fit of 0.991 in predicting dynamic stability, with a mean percentage of relative error (MAPE) of 6.15% between measured and predicted values. This underscores the feasibility of using BP neural networks in predictive dynamic stability models. Full article

This work aimed to investigate the effects of aging on the microstructures and rheological properties of modified asphalt with a GO/SBS composite, since the styrene–butadiene–styrene block copolymer is potentially compatible with graphene oxide (GO). The GO/SBS composites, which were used as a kind of modifier, were prepared via the solution-blending method. GO/SBS composites with varying GO contents were employed to prepare the GO/SBS-compound-modified asphalt (GO/SBS-MA). Then, the GO/SBS-MA underwent PAV (pressure aging vessel) or UV (ultraviolet) aging tests to simulate different aging circumstances. The microstructures of the asphalt binders were studied using FTIR (Fourier-transform infrared spectroscopy) and AFM (atomic force microscope) tests. Moreover, DSR (dynamic shear rheometer) and BBR (bending beam rheometer) experiments were carried out to investigate the rheological properties of the GO/SBS-MA. The results showed that the addition of GO improved the high-temperature stability of the asphalt binder while slightly impairing its performance at low temperatures. GO restrained the formation of carbonyl and sulfoxide groups as well as the breakdown of C=C bonds in the polybutadiene (PB) segment, promoting the anti-aging performance of GO/SBS-MA. Furthermore, the interactions between the GO/SBS and the asphalt binder resulted in the formation of needle-like aggregates, enhancing the stability of the asphalt binder. The asphalt binders with a higher content of graphene oxide (GO) exhibited not only a better high-temperature performance, but also a better aging resistance. It was concluded that the macroscopic properties and microstructures were significantly affected by GO, and a moderate increase in the amount of GO could contribute to a better aging resistance for GO/SBS-MA. Full article

Bio-fillers are intensively studied for advanced polymer composite circular design and production. In this context, the algal biomass may be considered an important and relatively low-cost resource, when harvested as a by-product from wastewater treatment plants. The biomass of the algal species Chlorella vulgaris is frequently used in this type of environmental process, and its macro constituents’ composition ranges from around 15–25% carbohydrates, 10–20% lipids, and 50–60% proteins. Poly (styrene-butadiene-styrene) (SBS) copolymers have a matrix composed of glassy polystyrene domains connected by flexible polybutadiene segments. Although the physical-mechanical properties of SBS copolymers recommend them for many industrial applications, they have the drawback of low biodegradability. This study aimed to assess the aerobic biodegradability of polymer composites by integrating biomass from Chlorella vulgaris at varying mass percentages of 5, 10, and 20% into SBS copolymer composites. Biodegradation tests were conducted under industrial composting conditions (58 °C and 50% relative humidity) for 180 days. The biodegradability of materials was evaluated by measuring the CO₂ produced in each vessel during the study period. Potential correlations between the amount of carbon dioxide released and the percentage of biomass added to the polymer matrix were examined. Structural and morphological changes were assessed using Fourier Transform infrared spectroscopy (FTIR), thermal analysis (DSC), and scanning electron microscopy (SEM). Physical and chemical testing revealed a decrease in sample density after the industrial composting test, along with noticeable changes in melt flow index (MFI). The observed physical and chemical changes, coupled with FTIR, SEM, and DSC data, indicate increased cross-linking and higher porosity in biodegraded polymer structures with higher biomass content. This behavior is likely due to the formation of cross-linked connections between polymer chains and polypeptide chains resulting from protein degradation, enhancing connections between polystyrene units facilitated by peptide bonds with the benzene units of the styrene blocks within the polymer matrix. Full article

The preparation of polymer composites that incorporate material of a biogenic nature in the polymer matrices may lead to a reduction in fossil polymer consumption and a potentially higher biodegradability. Furthermore, microalgae biomass as biogenic filler has the advantage of fast growth and high tolerance to different types of culture media with higher production yields than those provided by the biomass of terrestrial crops. On the other hand, algal biomass can be a secondary product in wastewater treatment processes. For the present study, an SBS polymer composite (SBSC) containing 25% (w/w) copolymer SBS1 (linear copolymer: 30% styrene and 70% butadiene), 50% (w/w) copolymer SBS2 (linear copolymer: 40% styrene and 60% butadiene), and 25% (w/w) paraffin oil was prepared. Arthrospira platensis biomass (moisture content 6.0 ± 0.5%) was incorporated into the SBSC in 5, 10, 20, and 30% (w/w) ratios to obtain polymer composites with spirulina biomass. For the biodegradation studies, the ISO 14855-1:2012(E) standard was applied, with slight changes, as per the specificity of our experiments. The degradation of the studied materials was followed by quantitatively monitoring the CO₂ resulting from the degradation process and captured by absorption in NaOH solution 0.5 mol/L. The structural and morphological changes induced by the industrial composting test on the materials were followed by physical–mechanical, FTIR, SEM, and DSC analysis. The obtained results were compared to create a picture of the material transformation during the composting period. Thus, the collected data indicate two biodegradation processes, of the polymer and the biomass, which take place at the same time at different rates, which influence each other. On the other hand, it is found that the material becomes less ordered, with a sponge-like morphology; the increase in the percentage of biomass leads to an advanced degree of degradation of the material. The FTIR analysis data suggest the possibility of the formation of peptide bonds between the aromatic nuclei in the styrene block and the molecular residues resulting from biomass biodegradation. It seems that in industrial composting conditions, the area of the polystyrene blocks from the SBS-based composite is preferentially transformed in the process. Full article

Thermoresponsive sol–gel transition polymers are of significant interest because of their fascinating biomedical applications, including as drug reservoirs for drug delivery systems and scaffolds for tissue engineering. Although extensive research has been conducted on lower critical solution temperature (LCST)-type sol–gel transition polymers, there have been few reports on upper critical solution temperature (UCST)-type sol–gel transition polymers. In this study, we designed an ABA-type triblock copolymer composed of a poly(ethylene glycol) (PEG) block and zwitterionic polymer blocks that exhibit UCST-type thermoresponsive phase transitions. A sulfobetaine (SB) monomer with both ammonium and sulfonate (–SO₃) groups in its side chain or a sulfabetaine (SaB) monomer with both ammonium and sulfate (–OSO₃) groups in its side chain was polymerized from both ends of the PEG block via reversible addition–fragmentation chain-transfer (RAFT) polymerization to obtain PSB-PEG-PSB and PSaB-PEG-PSaB triblock copolymers, respectively. Although an aqueous solution containing the PSB-PEG-PSB triblock copolymer showed an increase in viscosity upon cooling, it did not undergo a sol-to-gel transition. In contrast, a sol-to-gel transition was observed when a phosphate-buffered saline containing PSaB-PEG-PSaB was cooled from 80 °C to 25 °C. The PSaB blocks with –OSO₃ groups exhibited a stronger dipole–dipole interaction than conventional SB with –SO₃ groups, leading to intermolecular association and the formation of a gel network composed of PSaB assemblies bridged with PEG. The fascinating UCST-type thermoresponsive sol–gel transition properties of the PSaB-PEG-PSaB triblock copolymer suggest that it can provide a useful platform for designing smart biomaterials, such as drug delivery reservoirs and cell culture scaffolds. Full article

SBS (styrene-butadiene-styrene block copolymer) is a thermoplastic elastomer with properties most similar to rubber. SBS asphalt modifier is mainly composed of a styrene-butadiene-styrene block copolymer with a certain amount of additives and stabilizers. SBS-modified asphalt binder has always been the most commonly used pavement material both domestically and internationally. However, conventional wet-process SBS-modified asphalt binder requires manufacturers to produce it in advance and transport it to a mixing plant for blending. This has provided an opportunity for unscrupulous businesses to reduce the amount of SBS by adding other substances, allowing inferior asphalt binder to pass inspections undetected. At the same time, conventional wet-process SBS-modified asphalt tends to undergo phase separation and experience a decline in performance as the storage time increases. However, dry-process SBS-modified asphalt can be directly added at the mixing plant, effectively addressing the issues associated with conventional wet-process SBS-modified asphalt. It also helps to reduce environmental pollution to a certain extent. This study investigates the extraction process of dry-process SBS-modified asphalt binder. It clarifies the performance and modification mechanisms of two types of dry-process SBS-modified asphalt binder at different dosages through various testing methods, including basic indicators, rheological properties, infrared spectroscopy, and fluorescence microscopy. The results indicate that due to the incorporation of oil, crosslinker, solubilizer, and other substances into dry-process SBS modifier, there is a small amount of chemical reaction with asphalt in the melting process. The high- and low-temperature properties and fatigue properties of the two dry-process SBS-modified asphalt binders at a 7% dosage are close to wet SBS-modified asphalt binder at a 5% dosage. Full article

Antimony and arsenic, which have a high carcinogenicity, should be removed depending on their ionic charge in water. Therefore, we attempted to confirm the adsorption characteristics of antimony and arsenic considering ionic charge to improve removal efficiency. We used palm-based activated carbon (PAC), coal-based activated carbon (CAC), modified activated carbon (MAC), styrene-divinylbenzene copolymer (SP825), activated alumina (AA), and zeolite as adsorbents for antimony and arsenic. Negatively charged adsorbents (CAC, PAC, MAC, and zeolite) with similar zeta potentials showed better removal efficiency as the surface area increased. However, SP825, which is almost neutral, and AA, which is positively charged, exhibited a high removal efficiency (100%) for arsenic and Sb(V), which are anions, regardless of surface area. However, due to the price, coal-based activated carbon or palm-based activated carbon is considered more advantageous than using AA or SP825. Last, during the arsenic adsorption process, As(III) was oxidized to As(V) due to Fe(II) contained in activated carbon. The addition of activated carbon can improve oxidation efficiencies of As(III) before coagulation and precipitation, in which As(V) is easier to remove than As(III). Full article