Thyssensummers0787

SEM images revealed good adhesion between the additives and the PLA matrix. However, the additives induced faster solidification and showed larger voids in the 3D printing, which indicated lower layer adhesion as compared to neat PLA. It can be noted that the combination of the additives and the optimized 3D printing conditions would be obtain superior mechanical performance even layer adhesion has been restricted.Injection molding is an effective mass production process for plastic, partly due to a number of advantages such as complex shape moldability, material selectivity, and a rapid process cycle. However, highly labor-based conventional production restrains the development of the industry. Experience-driven molding setups are used to trial the mold process, and also for quality checking the molded part for mass production. selleck inhibitor There is no effective solution for maintaining the production stability and defect-free adjustment. This study aimed to establish scientific packing pressure setup technology to optimize the molded part quality and the stability of consecutive production. The dynamic packing pressure setup technology for molded part quality and the process stability were investigated. This not only achieves the optimization of the packing pressure setup, but the stabilization of quality in mass production. Four major qualities were discussed in this study including tensile strength, regional deviation on shrinkage, total shrinkage, and warpage. The qualities improved by up to 3.9%, 92.9%, 41.9%, and 9.2%, respectively. A series of pilot runs of 300 cycles for two packing pressure control methods were tested to investigate the stability of the qualities. Dynamic packing pressure control improved the weight replication by 54%, reduced total shrinkage by 23%, and improved the warpage by 12%.Nonisocyanate polyurethane materials with pending alcohol groups in the polymeric chain were synthesized by polyaddition reaction of bis(cyclic carbonates) onto diamines. For the platform molecule, 1,4-butanediol bis(glycidyl ether carbonate) (BGBC, 1) was used. The polyaddition reaction of 1 onto a wide range of diamines with different electronic and physical properties was explored. All PHUs were obtained quantitatively after 16 h at 80 °C temperature in MeCN as solvent. The low nucleophilicity of L-lysine has proven unable to ring-open the cyclic carbonate and, thus, no reaction occurred. The addition of DBU or TBD as the catalyst was tested and allows the obtention of the desired PHU. However, the presence of strong bases also led to the formation of polyurea fragments in the new PHU. The different poly(hydroxyurethane) materials were characterized using a wide range of spectroscopic techniques such as NMR, IR, MALDI-ToF, and using GPC studies. The thermal properties of the NIPUs were investigated by DSC and TGA analyses. Moreover, reactions employing different monomer ratios were performed, obtaining novel hydroxycarbamate compounds. Finally, sequential and one-pot experiments were also carried out to synthesize the PHUs polymers in one-step reaction.Acrylamide-methacrylic acid copolymer named P (AM-co-MAA) was synthesized via aqueous solution polymerization, and then mixed with crosslinker, flame retardants and initiators to prepare multifunctional transparent flame-retarded hydrogels with transparency, fire resistance and anti-ageing property. The results show that the application of multifunctional transparent flame-retarded hydrogel imparts high level of transparency and excellent fire resistance to the fire-resistant glass, and the light transmittance and fire resistance of the flame-retarded hydrogel increases with the increasing mass ratio of AM to MAA in P(AM-co-MAA). When the mass ratio of AM to MAA is 41, the obtained P(AM-co-MAA) imparts the lowest backside temperature of 130 °C at 3600 s and highest light transmittance of 86.1% to the transparent flame-retarded hydrogel. TG and DSC analysis show that the addition of P(AM-co-MAA) increases the thermal stability of the transparent flame-retarded hydrogels due to the formation of numerous hydrogen bonds via the complexation between amide and carboxyl groups. Accelerated ageing test indicates that the transparent flame-retarded hydrogel containing P(AM-co-MAA) exerts durable fire resistance and transparency, and the ageing resistance of the transparent flame-retarded hydrogel depends on the mass ratio of AM to MAA in P(AM-co-MAA). Therefore, this study provides a promising strategy to prepare a novel multifunctional transparent flame-retarded hydrogel with excellent light transmittance, fire resistance and anti-ageing properties.CF4 has a global warming potential of 6500 and possesses a lifetime of 50,000 years. In this study, we modified the HZSM-5 catalyst with Ce and sulfuric acid treatment. The S/Ce/HZSM-5 catalyst achieves 41% of CF4 conversion at 500 °C, which is four times higher than that over Ce/HZSM-5, while the HZSM-5 exhibits no catalytic activity. The effects of modification were studied by using NH3-TPD, FT-IR of pyridine adsorption, and XPS methods. The results indicated that the modification, especially the sulfuric acid treatment, strongly increased the Lewis acidic sites, strong acidic sites, and moderate acidic sites on catalysts, which are the main active centers for CF4 decomposition. The mechanism of acidic sites increases by modification and CF4 decomposition is clarified. The results of this work will help the development of more effective catalysts for CF4 decomposition.In order to produce a high-viscosity asphalt and mixtures that can be used for ultra-thin overlays, high contents of Styrene-butadiene-styrene (SBS, 5%, 6%, 7%), styrene butadiene rubber (SBR, 1%, 2%, 3%) and micro carbon fiber (MCF, 0.8%) were used to modify conventional asphalt to prepare high-viscosity modified asphalt suitable for this purpose. The performance of the modified asphalts was evaluated by conventional index, kinematic viscosity, dynamic shear rheological test (DSR), multiple stress creep recovery test (MSCR), and bending beam rheometer test (BBR). The road performance of the modified asphalt mixtures was evaluated by high-temperature rutting, low-temperature bending, freeze-thaw splitting, fatigue, speckle, anti-skid, and water seepage tests. The results show that increasing the content of SBS can improve the high-temperature deformation resistance, low-temperature failure strain, kinematic viscosity, and viscosity toughness of modified asphalt, and the optimum content of SBS was 6%. SBR can improve the high-temperature performance, kinematic viscosity, and water damage resistance of modified asphalt, and the optimum dosage was 2%. Compared with 5% SBS-modified asphalt mixture, the dynamic stability, low-temperature failure strain, and freeze-thaw splitting strength ratio of 6% SBS + 0.8% MCF composite-modified asphalt mixture were increased by 48.7%, 24.7%, and 5.2% respectively. Compared with the 5% SBS-modified asphalt, the same characteristics of the 2% SBR + 5% SBS + 0.8% MCF composite-modified asphalt increased by 127.1%, 13.5%, and 5.5%, respectively. Compared with 5% SBS-modified asphalt, the fatigue performance of 6% SBS + 0.8% MCF-modified asphalt was improved by 32.2%. The kinematic viscosity of 6% SBS + 0.8% MCF and 5% SBS + 0.8% MCF + 2% SBR modified asphalt met the performance requirements of high-viscosity asphalt and had excellent road performance. It can be applied to ultra-thin overlays to optimize its adhesion with the original pavement.This study followed the approach of dispersing and localizing carbon nanotubes (CNTs) in nanostructured domains of block copolymers (BCPs) by shortening the CNTs via ball milling. The aim was to selectively tune the electrical and mechanical properties of the resulting nanocomposites, e.g., for use as sensor materials. Multiwalled carbon nanotubes (MWCNTs) were ground into different size fractions. The MWCNT length distribution was evaluated via transmission electron microscopy and dynamic light scattering. The nanostructure of the BCPs and the glass transition temperatures of the PB-rich and PS phases were not strongly affected by the addition of CNTs up to 2 wt%. However, AFM and TEM investigations indicated a partial localization of the shortened CNTs in the soft PB-rich phase or at the interface of the PB-rich and PS phase, respectively. The stress-strain behavior of the solution-mixed composites differed little from the mechanical property profile of the neat BCP and was largely independent of CNT amount and CNT size fraction. Significant changes could only be observed for Young's modulus and strain at break and may be attributed to CNT localization and small changes in morphology. For nanocomposites with unmilled CNTs, the electrical percolation threshold was less than 0.1 wt%. As the CNTs were shortened, the resistivity increased and the percolation threshold shifted to higher CNT contents. Composites with CNTs ground for 7.5 h and 13.5 h showed no bulk conductivity but significantly decreased surface resistivity on the bottom side of the films, which could be attributed to a sedimentation process of the grind and thereby highly compressed CNT agglomerates during evaporation.Several recent advances have emerged in biotherapy and the development of personal drugs. However, studies exploring effective manufacturing methods of personal drugs remain limited. In this study, solid drugs based on poly(ethylene glycol)diacrylate (PEGDA) hydrogel and doxorubicin were fabricated, and their final geometry was varied through UV-light patterning. The results suggested that the final drug concentration was affected by the geometrical volume as well as the UV-light exposure time. The analysis of PEGDA showed no effect on the surrounding cells, indicating its high biocompatibility. However, with the addition of doxorubicin, it showed an excellent therapeutic effect, indicating that drugs inside the PEGDA structure could be successfully released. This approach enables personal drugs to be fabricated in a simple, fast, and uniform manner, with perfectly tuned geometry.Natural rubber latex (NRL) is a polymer (blend) extracted from the milky sap of para rubber trees. Due to being a natural biopolymer, NRL contains various proteins that may be allergenic to humans when in skin contact. Attempts have been made to use deproteinized natural rubber (DPNR) instead of impure NRL, and the final properties of these two types of rubber tend to differ. Thus, the correlations between their chemistry and properties are of focal interest in this work. DPNR was prepared by incubating NRL with urea, followed by aqueous washing/centrifugation. The physical, mechanical, and dynamic properties of incubated NRL before and after washing/centrifugation were examined to distinguish its influences from those of incubation with urea. According to the findings, the proteins, phospholipids, and chain entanglements were responsible for natural polymer networks formed in the NR. Although the proteins were largely removed from the latex by incubation, the properties of high ammonia natural rubber (HANR) were still maintained in its DPNR form, showing that other network linkages dominated over those contributed by the proteins. In the incubated latex, the naturally occurring linkages were consistently reduced with the number of wash cycles.