Polyether Amine Research Articles

Fabrication of PVC-based electromagnetic interference shielding composite film by positively charged SMA enhancing the dispersibility of carbon nanomaterial

To address the weak binding force and poor dispersion stability of carbon (C) nanoparticles in current non-covalent modification methods, we employed organic amine-grafted styrene maleic anhydride copolymers (SMA-N) to modify C nanoparticles (C@SMA-N) through π–π conjugation and positive charge interactions. The obtained C@SMA-N has excellent dispersion in N, N-dimethylacetamide (DMAc), which is attributed to the enhanced steric hindrance and electrostatic repulsion from the grafted organic amine chains. To study the impact of surface modification on the electromagnetic interference shielding effectiveness (EMI SE), C@SMA-N was used as a conductive filler in polyvinyl chloride (PVC) composite films, which exhibits a higher EMI SE performance than pristine C nanoparticles. Particularly, the obtained C@SMA-N using polyether amine (PEA) (C@SMA-PEA) exhibits a better EMI SE performance. By optimizing the SMA-PEA grafting parameters, the PVC/C@SMA-PEA composite films transition from insulators to conductors at a C@SMA-PEA content of 0.3 wt%. To achieve a higher EMI SE performance, the filler content, mixed filler composition, and film thickness were optimized. The results indicate that with a total filler content of 20 wt% and a mixed filler comprising fibrous form carbon nanotubes (CNT) and particles form carbon black (CB) in a 10:1 mass ratio (CB@SMA-PEA to CNT@SMA-PEA), the composite film has a thickness of 0.08 mm and an EMI SE value of 20.2 dB. Increasing the thickness to 0.2 mm enhances the EMI SE value to 31.5 dB. These findings indicate that thinner films have a higher EMI SE performance and promising application prospects in the field of electromagnetic shielding.

PH- and temperature-dual responsive polymer emulsion for rapid release of drag reducer

Slick water fracturing fluid is widely used in major oil fields due to its low cost and high drag reduction. Polyacrylamide emulsions drag reducers play a decisive role in slick water fracturing. The dissolution rate of polymer emulsions drag reducers was increased by adding hydrophilic surfactants, but the stability of the emulsions is poor, which limits its wide application. In order to solve the contradiction between the stability of polymer emulsion and rapid release of drag reducer. Here, a P(AA-AM-AMPS) polymer emulsion drag reducer with dual stimulation response of pH and temperature was designed. Surfactant (D400/OA) with dual responses to pH and temperature is synthesized by using oleic acid (HOA) and polyether amine 400 (D400). D400/OA shows a remarkable pH- and temperature-responsive behavior due to the pH- and temperature-induced structural transformation of D400/OA. Interestingly, D400/OA-stabilized monomer emulsion exhibits an obvious pH- and temperature-induced structural transformation. Meanwhile, The D400/OA-stabilized monomer emulsion has remarkable stability, which benefits the inverse emulsion polymerization of P(AM-AA-AMPS) polymer. The obtained P(AM-AA-AMPS) polymer emulsion maintain stability whose particle size nearly unchanged by storing for 15 days. Interestingly, P(AM-AA-AMPS) polymer emulsion can be released completely by changing the pH or temperature of the aqueous solution. The apparent viscosity of P(AM-AA-AMPS) polymer, in either the alkaline (pH=10.31) solution of 25±2 °C or neutral (pH=7) solution of 70±2 °C, respectively required 40 s and 8 min to reached a maximum value of 96 mPa·s. The release rate of P(AM-AA-AMPS) polymer emulsion is further enhanced under the dual responsive of temperature (70±2 ℃) and pH (10.31) and it takes only 20 s, In addition, the drag reduction rate of P(AM-AA-AMPS) polymer emulsion is 72 % when completely released under the dual responsive of temperature and pH, showing a remarkable drag reduction property. The D400/OA-stabilized P(AM-AA-AMPS) polymer emulsion are expected to meet the demand for the production enhancement of the oil and gas reservoirs.

Improving shale hydration inhibition with hydrophobically modified graphene oxide in water-based drilling fluids

Frequent wellbore instability issues caused by shale hydration and dispersion are encountered in water-based drilling fluids. In order to mitigate shale hydration, a hydrophobic graphene oxide (HGO) was prepared as a new shale inhibitor and characterized. The effectiveness of HGO in inhibiting shale hydration was evaluated through hydration expansion, hydration dispersion, and bentonite sheets immersion tests. The expansion height of bentonite in HGO (3.87 mm) was lower than that of commercial shale inhibitors potassium chloride (KCl, 4.64 mm) and polyether amine (PA, 4.33 mm). The shale recovery rate in HGO at 80 °C was 86.25 %, which was superior to KCl (46.60 %) and PA (78.25 %). Furthermore, the morphology of bentonite sheet remained more intact after immersion in HGO. Additionally, the inhibitory mechanism of HGO was studied in-depth, employing zeta potential, particle size, surface tension, wettability, capillary rise height, and scanning electron microscopy (SEM) tests. By virtue of electrostatic attraction, HGO could tightly adsorb to the shale surface, resulting in a hydrophobic blocking membrane, thereby greatly reducing water infiltration. Following interaction with shale at a concentration as low as 0.5 %, the water contact angle exhibited a notable enhancement, rising from 22.49° to 86.69°. And it could also decrease the capillary self-suction capacity of shale, further reducing water adsorption. Consequently, HGO exhibited significant potential for inhibiting hydration in shale drilling.

Optically clear pressure‐sensitive adhesive with flexible crosslinking agent for high recovery efficiency, low energy storage modulus, and excellent folding resistance

AbstractOptically clear pressure‐sensitive adhesive (OCA) possesses exceptional optical properties and exhibits pressure‐sensitive adhesion, making it widely utilized in the adhesive layers of various electronic display devices. However, the increasing popularity of foldable mobile phones in recent years has imposed new requirements on the overall performance of OCA. Conventional pressure‐sensitive adhesives can enhance recoverability through cross‐linking but often demonstrate inadequate adhesive strength. In this study, three long‐chain crosslinking agents (CL) were synthesized using hydroxyethyl acrylate (HEA), dicyclohexylmethane diisocyanate (HMDI), polypropylene glycol (PPG), polyether amine (PEA), and hydroxyl‐terminated polybutadiene (R45V). The long‐chain CL agent contains numerous flexible segments that improve the recovery capability of the OCA while maintaining a certain level of adhesion. The optical clear pressure‐sensitive adhesive, crosslinked by three flexible crosslinkers, exhibits a low glass transition temperature (−60 to −40°C) and a low storage modulus (<0.1 MPa), along with an appropriate 180° stripping force (6–8 N/25 mm). Optically transparent pressure‐sensitive adhesives demonstrate excellent recovery properties (>85%), high light transmittance (>92%), and exceptional flexibility. Moreover, compared to market products, the optically transparent pressure‐sensitive adhesive shows superior folding resistance (>100,000 times). This indicates its suitability for applications in flexible optical displays such as foldable mobile phones and wearable electronics.

Achieving the hydrophobic alteration by functionalized nano-silica for improving shale hydration inhibition

Shale hydration is the primary cause of wellbore instability during drilling processes. In this study, two non-fluorinated silane-coupling agents, octyltriethoxysilane (OTES) and (3-Aminopropyl) triethoxysilane (APTES), were grafted onto the nano-silica surface to develop a hydrophobic material (SHM). Various performance characterizations, including infrared spectroscopy, thermogravimetric analysis, surface tension, wetting alteration, capillary self-suction height, bentonite expansion, and shale dispersion, were employed to investigate the shale inhibition properties of SHM comprehensively. Experimental results revealed that SHM could significantly improve shale hydration inhibition. For instance, in a 2 % SHM liquids, the shale hot rolling recovery rate increased from 25.39 % to 83.78 %, and the bentonite expansion height decreased from 7.65 mm to 2.80 mm. The inhibition performance was notably superior to potassium chloride (KCl) and polyether amine (PEA). Inhibition mechanisms analysis unveiled that the outstanding inhibitory effect of SHM was achieved through electrostatic adsorption, wettability alteration, and surface tension reduction. Firstly, SHM contained numerous amine groups that could demonstrate strong adsorption on the clay surface through electrostatic and hydrogen bonding interactions. Secondly, with long hydrophobic alkyl chains, it formed a highly hydrophobic film enveloping the shale surface, effectively preventing water from invading. Thirdly, it reduced liquid surface tension, further minimizing the water infiltration. As a result, the use of SHM significantly enhanced shale hydration inhibition during the shale drilling process.

A 3-D nanostructure polyhedral oligomeric silsesquioxane as a (co)-crosslinker of an epoxy resin

Epoxy resins have outstanding properties with variety uses especially in high performance engineering applications. However, high degree of crosslinking density makes them rigid and brittle. Many attempts have been used to improve mechanical properties, especially toughness. In the current work, synergistic properties of using the polyhedral oligomeric silsesquioxane nanostructure (POSS) and polyether amine chains has been used to improve toughness and mechanical properties especially modulus by using the synthesized structure as co-curing agent in epoxy resin. The characteristic analysis showed that the structure of the synthesized molecule is a POSS core with four polyether amine chains and four glycidyloxy propyl chains attached to the siloxane cage. The results indicated that using the synthesized structure (GA-POSS) as co-curing agent has two effects: it acted like a reinforcing agent and improve glass transition temperature, toughness and Young’s modulus. Also, it increased distance between crosslinks which led to increase of tan δ and elongation at break. However, these effects did not observed when this nano-molecule worked as cross linker or when the POSS structure doesn’t have soft long chains because just in the case of using GA-POSS as co-curing agent hard-soft-hard state is formed which leads to high mechanical and toughness properties, simultaneously.

Diels-Alder Network Blends as Self-Healing Encapsulants for Liquid Metal-Based Stretchable Electronics.

Two dynamic covalent networks based on the Diels-Alder reaction were blended to exploit the properties of the dissimilar polymer backbones. Furan-functionalized polyether amines based on poly(propylene oxide) (PPO) FD4000 and polydimethylsiloxane (PDMS) FS5000 were mixed in a common solvent and reversibly cross-linked with the same bismaleimide DPBM. The morphology of the phase-separated blends is primarily controlled by the concentration of backbones. Increasing the PDMS content of the blends results in a dilute droplet morphology at 25 wt %, with a growing size and concentration of droplets and the formation of two separate PPO- and PDMS-rich layers at 50 wt %. Further increasing the PDMS content to 75 wt % leads to larger droplets and a thicker layer of the secondary phase. The hydrophobic PDMS phase creates a barrier against water, while the more hydrophilic PPO phase enhances the resistance against oxygen diffusion. Lowering the maleimide-to-furan stoichiometric ratio resulted in a decrease in cross-link density and thus more flexible and stretchable encapsulants. Changes in the stoichiometric ratio also affected the phase morphology due to resulting changes in phase separation and network formation kinetics. Lowering the stoichiometric ratio also resulted in enhanced self-healing properties of 96% at room temperature as a consequence of the increased chain mobility in the blended networks. The self-healing blends were used to encapsulate liquid metal circuits to create stretchable strain sensors with a linear electro-mechanical response without much drift or hysteresis, which could be efficiently recovered by 90% after the damage-healing cycles.

One-step facile pathway synthesis of PAPXD/1214-PEA thermoplastic elastomer: Structure and properties

In this study, a novel and facile one-step synthesis route was conducted to prepare semi-aromatic polyamide elastomer (PAPXD/1214-PEA) with p-phenylenediamine, dodecane diamine, dodecanedioic acid and polyether amine (PEA) as monomers. A systematic investigation has been conducted into the effect of hard segment content on the thermal, mechanical and solvent resistance of polymers when semi-aromatic polyamides are used as hard segments. It was found that the melting point of the copolymers gradually increased from 191.2 °C to 231.5 °C with the hard segment content increased from 39 % to 76 %, while the Vicat softening temperature (VST) enhanced from 103.2 °C to 192.2 °C. Compared with the commercial polyamide elastomer Pebax@ (produced by Arkema Inc) with similar hard segment contents, the VST of PAPXD14/1214-PEA were 17.4–66.2 °C higher. The mechanical performance of these elastomers was also largely improved with tensile strength increasing from 15.1 to 40.6 MPa, Young's modulus from 28.2 to 168.7 MPa, toughness from 91.1 to 170.7 MJ/m3. In addition, the solvent resistance properties of PAPXD14/1214-PEA was compared with the commercial polyamide elastomer Pebax@. After soaking in hydrochloric acid for 24 h, the tensile strength of PAPXD/1214-PEA with the hard segment content increased from 50 % to 63 % decreased down to 9.4 and 14.4 MPa, respectively. While the commercial polyamide elastomer Pebax@ (with similar hard segment content) decreased down to 1.5 and 4.3 MPa, indicating the commercial polyamide elastomer products were deteriorated. This suggests the corrosion resistance of the synthesized PAPXD/1214-PEA is much better than that of commercial product, and these semi-aromatic polyamide elastomers can be potentially applied in some harsh service environment especially for high temperature and corrosion sealing.

Fabrication of fully bio-based malleable thermoset derived from cellulose, furfural and plant oil for advanced capacitive sensor

Fabrication of sustainable bio-based malleable thermosets (BMTs) with excellent mechanical properties and reprocessing ability for applications in electronic devices has attracted more and more attention but remains significant challenges. Herein, the BMTs with excellent mechanical robustness and reprocessing ability were fabricated via integrating with radical polymerization and Schiff-base chemistry, and employed as the flexible substrate to prepare the capacitive sensor. To prepare the BMTs, an elastic bio-copolymer derived from plant oil and 5-hydroxymethylfurfural was first synthesized, and then used to fabricate the dynamic crosslinked BMTs through Schiff-base chemistry with the amino-modified cellulose and polyether amine. The synergistic effect of rigid cellulose backbone and the construction of dynamic covalent crosslinking network not only achieved high tensile strength (8.61 MPa) and toughness (3.77 MJ/m3) but also endowed the BMTs with excellent reprocessing ability with high mechanical toughness recovery efficiency of 104.8 %. More importantly, the BMTs were used as substrates to fabricate the capacitive sensor through the CO2-laser irradiation technique. The resultant capacitive sensor displayed excellent and sensitive humidity sensing performance, which allowed it to be successfully applied in human health monitoring. This work paved a promising way for the preparation of mechanical robustness malleable bio-thermosets for electronic devices.

Metal-organic framework-based porous liquids via surface functionalization engineering for selective gas adsorption

Porous liquids (PLs) combine the distinct porosity of solids with the fluidity of liquids, offering new solutions for carbon capture, membrane separation, and more. This study introduces the development of unique UIO-66-PLs through a meticulous surface functionalization strategy, using surface-modified UIO-66-(OH)2 with the organic oligomer SIT8378.3 (SIT) and polyether amines (PEAs) of various molecular weights (M1000, M2070, and M3085) as the hindering solvents. The resulting UIO-66-PLs exhibit exceptional stability and dispersibility in both aqueous and organic environments. Importantly, benefiting from preserving UIO-66-(OH)2′s porosity in PLs, the affinity of PEAs’ ethylene oxide segments for CO2 via Lewis acid-base interactions, and additional free space within organic chains, UIO-66-PLs revealed enhanced CO2 adsorption capabilities, particularly for CO2 over N2. Encouragingly, CO2 adsorption of UIO-66-PLs was enhanced by 117.54 % (UIO-66-M1000), 106.01 % (UIO-66-M2070), and 22.45 % (UIO-66-M3085) in capacity relative to the respective pure organic outer layer. It is also observed that while surface engineering improves gas adsorption performance, PEAs with a high molecular weight may partially block UIO-66-(OH)2 pores, decreasing gas adsorption capacities. Our research showcases the potential of UIO-66-PLs in gas storage and separation applications, offering a new approach to developing materials functionalized with customized organic molecular weights for advanced CO2 capture technologies.

Preparation and performance of carboxyl modified NdFeB and derived magnetic self-healing PU composites

With the rapid development of today’s society, magnetic self-healing materials are widely used in many fields due to their excellent magnetism and self-healing ability. This article presents a magnetic self-healing composite with good mechanical, self-healing and magnetic properties and magnetic drive performance. Tetraethyl orthosilicate (TEOS), silane coupling agent and succinic anhydride (SA) were used for surface modification of NdFeB magnetic particles (MPs) and NdFeB@SiO2-COOH MPs was synthesized. Iron(III) ions were added to the self-polymerization process of the natural small molecule thioctic acid (TA) to form the PTA-Fe prepolymer. PTA-Fe prepolymer, isophorone diisocyanate (IPDI) and polyether amine (PEA) reacted to synthesis PTA-Fe-PU matrix with good self-healing performance at room temperature. The prepared NdFeB@SiO2-COOH MPs was mixed with the self-healing matrix and cured to obtain the magnetic room-temperature self-healing composite MPTA-Fe-PU. The best tensile strength of the composite was 7.31 MPa and the ultimate elongation was 833 %. After the prepared MPTA-Fe-PU sample strip was completely cut, the incision on the surface almost disapeared and the tensile strength recovered to 6.35 MPa after 12 h self-healing at room temperature. The self-healing efficiency was up to 87 %. The highly efficient self-healing properties were mainly derived from the disulfide bonds exchange reaction and iron(III) ion coordination in the matrix.

Innovative Application of Polyether Amine as a Recyclable Catalyst in Aerobic Thiophenol Oxidation

Polyether amines are versatile compounds characterized by a flexible structure, consisting of polyoxypropylene and polyoxyethylene as the backbone, with amine groups at each end. They have widespread applications in various industrial processes and daily life. Despite their versatility, the utilization of polyether amines as base catalysts is rare. In this study, one kind of three-arm polyether amine 1 was employed as an environmentally friendly, cost-effective catalyst for the aerobic oxidation of thiophenols, leading to the synthesis of disulfides. The oxidative coupling of thiols serves as a fundamental pathway for the production of disulfides, which are vital in both chemical and biological processes. In contrast to known methods for thiol oxidation, this polyether amine-based catalytic process eliminates the need for expensive stoichiometric oxidants and minimizes the formation of over-oxidized by-products. Using a mere 0.5 mol % of the polyether amine 1 as the catalyst, a remarkable > 96% yield was achieved for all 16 tested substrates, encompassing a diverse range of functional groups, under the catalytic aerobic oxidation conditions. Furthermore, it is noteworthy that over 90% of the polyether amine catalyst can be efficiently recovered for reuse without loss of activity, making this a sustainable and cost-effective catalytic approach.

Seamlessly embedded microcapsules in self-repairing coatings: Improved compatibility and enhanced corrosion resistance recovery

Microcapsules, with polyether amine as the core repairing agent and polyether amine-cured epoxy as the shell, were prepared via the multiple emulsion polymerization and applied in an epoxy/polyether amine coating system on carbon steel surfaces. The microcapsules and the coating substrate have the same composition and are seamlessly connected by chemical bonds, akin to the direct injection of liquid healing agents into the substrate. When the repairing agent flows out, it will crosslink and cure with the epoxy groups in the substrate to achieve no difference self-repair. The characteristics of microcapsules were studied by scanning electron microscope (SEM), Fourier transform infrared (FTIR) and Thermal gravimetric (TG). The mechanical properties and corrosion resistance recovery of coatings loaded of coatings with different weight percentages of loaded microcapsules were investigated using tensile testing, electrochemical impedance spectroscopy (EIS) and neutral salt spray test (NSS). Results indicate that the 7 wt% microcapsules composite coating shows a 37.7 % increase in tensile strength and a 71.4 % increase in fracture toughness over pure epoxy coating. After immersing in saltwater for 7 days, the scratch sealing efficiency can reach 99.85 %. The coating system not only improved the compatibility between microcapsules and the substrate, but also enhanced the toughness of thermosetting brittle epoxy materials, giving it long-lasting anti-corrosion capability.

Polyethylene glycol diacid and jeffamine nanocomposites for high-energy supercapacitor with photoluminescence properties

Polymer dots improve ion transport and supercapacitor properties due to active functional groups on their surface. In this study, a new nanocomposite of polymer dot based on polyether amine D-230) Jeffamine (-nickel oxide (PDJA-NiO) was synthesized by a one-step method (quantum yield of 82.2 %). Also, a novel nanocomposite of polymer dot based on polyethylene glycol diacid and Jeffamine-nickel oxide (PDPJA-NiO) was synthesized in the same method and conditions to study the effect of polymers in improving the supercapacitor properties, (quantum yield of 78.84 %). The PDJA-NiO electrode and the PDPJA-NiO electrode were prepared, and the electrochemical analyses were performed. The new PDPJA-NiO specific capacitance and the new PDJA-NiO specific capacitance were obtained at about 527 F g−1 and 355 F g−1 at 1 A g−1. Also, two symmetric devices were made from the PDPJA-NiO nanocomposite (PDPJA-NiO/AC//AC/PDPJA-NiO) and the PDJA-NiO nanocomposite (PDJA-NiO/AC//AC/PDJA-NiO), that showed a specific capacitance of 123 F g−1 and 100 F g−1 at 1 A g−1, respectively. The PDPJA-NiO/AC//AC/PDPJA-NiO and the PDJA-NiO/AC//AC/PDJA-NiO supercapacitors exhibited maximum energy densities of 37.26 Wh kg−1 and 31.01 Wh kg−1. The illumination of white LED by both nanocomposites confirms the practical application of both nanocomposites.

Experimental and molecular dynamics study on thermal‐mechanical properties of epoxy shape memory polymers

AbstractExperimental and molecular dynamics simulations were employed to investigate epoxy shape memory polymers' thermal‐mechanical properties and shape memory characteristics, utilizing polyether amine and modified hexanediamine as curing agents following the material prerequisites for variable stiffness fixtures. Glass transition temperature and Young's modulus of epoxy shape memory polymers are characterized by dynamic mechanical analysis. The consistency of the glass transition temperature between the simulation model and the experimental findings verified the accuracy of the molecular dynamics simulation. The uniaxial tensile simulation revealed that non‐bond energy predominantly exerts its influence in stretch. After reaching the yield stress, the weight fraction of the curing agent affects the generation of internal pores, with the yield stress of systems exhibiting substantial pores being minor. Systems characterized by a higher weight fraction of curing agents are more prone to pore formulation. Simulation of shape memory properties demonstrates that the entropy resulting from differences in molecular weight impacts the simulated system's shape fixation ratio and shape recovery ratio.

A room‐temperature self‐healing anticorrosion coating of supramolecular polyurethane based on dynamic reversible quadruple hydrogen bond

AbstractThe contradiction between the migration rate of molecular chains and mechanical strength has always been a key factor affecting the practical application of self‐healing anticorrosion coatings. In this paper, a series of supramolecular self‐healing elastomers (SPU‐MP) were prepared by the reaction of diphenylmethane diisocyanate and polyether amine. The results shown that the proportion of polyetheramine D230 (D230) in molecular segments affects the hydrogen bond density between molecular chains, thereby affecting the self‐healing efficiency and mechanical strength of SPU‐MP. When the ratio of D230 and polyetheramine D400 (D400) is 2:8, the tensile fracture strength of SPU‐MP8 is 5.08 MPa, and the self‐healing efficiency reaches 82.1% after 10 h of repair at room temperature. Further increasing the ratio of D230 increases the relaxation time of the molecular chain due to the increase in hydrogen bond density, resulting in a decrease in the self‐healing efficiency of SPU‐MP. The results of electrochemical experiments and neutral salt spray experiments indicate that the anticorrosion coating prepared by SPU‐MP8 exhibits good self‐healing performance. After immersing in 3.5 wt.% NaCl solution for 35 days, the low‐frequency impedance modulus of the intact coating and the scratch coating were both higher than 107 Ω cm2, still shown good anticorrosion ability.

Effects of Polyether Amine Canopy Structure on Heavy Metal Ions Adsorption of Magnetic Solvent-Free Nanofluids.

Three Fe3O4 magnetic solvent-free nanofluids with different amine-based coronal layer structures are synthesized and characterized by using magnetic Fe3O4 as the core, silane coupling agent as the corona, and polyether amines with different graft densities and chain lengths as the canopy. The concentration of heavy metal ions after adsorption is measured by atomic absorption spectrometry (AAS) to study the effect of Fe3O4 magnetic solvent-free nanofluids on the adsorption performance of the heavy metal ions lead (Pb(II)) and copper (Cu(II)) in water. The adsorption of Fe3O4 magnetic solvent-free nanofluid was explored by changing external condition factors such as adsorption contact time and pH. Additionally, the adsorption model is established. The magnetic solvent-free nanofluid is separated from water by applying an external magnetic field to the system, and desorption and cyclic adsorption tests are carried out. Based on the adsorption mechanism, the structure design of Fe3O4 magnetic solvent-free nanofluid was optimized to achieve optimal adsorption performance.

Enhancing the physical properties of styrene-butadiene-styrene (SBS)-modified asphalt through polyetheramine-functionalized graphene oxide (PEA-GO) composites

To enhance the dispersion of graphene oxide (GO) in Styrene-butadiene-styrene (SBS) modified asphalt (SA) and the comprehensive physical properties of GO/SBS-modified asphalt (GSA), PEA-GO composites were prepared by grafting polyetheramine (PEA) onto GO for the preparation of PEA-GO/SBS-modified asphalt (PGSA). In this study, the chemical structure of PEA-GO was examined using fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The conventional properties of GSA and PGSA were analyzed. The effects of GO and PEA-GO on the high and low-temperature prevalent properties of SA were investigated by dynamic shear rheology (DSR) test and bending beam rheology (BBR) test. The adhesion properties of GSA and PGSA were investigated by surface free energy theory (SFE). The surface micro-morphology of GSA and PGSA and the dispersion state of GO in SA were analyzed using atomic force microscopy (AFM) and fluorescence microscopy (FM). The results showed that the characteristic absorption peaks of N-H, CH2-CH2, and C-N appeared in the FTIR diagram of PEA-GO. A new peak appeared in the XPS diagram: C-N. The high-temperature performance, low-temperature crack resistance, and adhesion of PGSA were superior to those of GSA. The size of the "bee structure" in PGSA is larger than in GSA, and PEA-GO demonstrates uniform dispersion in SA. This study serves as a reference for fine-tuning graphene oxide (GO) at the microscopic level to enhance the physical properties of GSA.

Reprocessing and Resource Utilization of Landfill Sludge—A Case Study in a Chinese Megacity

In the past, due to improper sludge treatment technology and the absence of treatment standards, some municipal sludge was simply dewatered and then sent to landfills, occupying a significant amount of land and posing a serious threat of secondary pollution. To free up land in the landfill area for the expansion of a large-scale wastewater treatment plant (WWTP) in Shanghai, in this study, we conducted comprehensive pilot research on the entire chain of landfill sludge reprocessing and resource utilization. Both the combination of polyferric silicate sulfate (PFSS) and polyetheramine (PEA) and the combination of polyaluminum silicate (PAS) and polyetheramine (PEA) were used for sludge conditioning before dewatering, resulting in dewatered sludge with approximately 60% moisture content. The combined process involved coagulation and sedimentation, flocculation, and oxidation to treat the leachate generated during dewatering. The treatment process successfully met the specified water pollutant discharge concentration limits for the leachate, with the concentration of ammonia nitrogen in the effluent as low as 15.6 mg/L. Co-incineration in a power plant and modification were applied to stabilize and harmlessly dispose of the dewatered sludge. The coal-generating system ran stably, and no obvious problems were observed in the blending process. In the modification experiment, adding 5% to 7% of the solidifying agent increased the sludge bearing ratio by 53% and 57%, respectively. This process effectively reduced levels of fecal coliforms and heavy metals in the sludge but had a less noticeable effect on organic matter content. The modified sludge proved suitable for use as backfill material in construction areas without requirements for organic matter. The results of this study provide valuable insights for a completed full-scale landfill sludge reclamation and land resource release project.

Novel Furfural-Derived Polyaldimines as Latent Hardeners for Polyurethane Adhesives.

Moisture-curing one-component polyurethane systems in adhesive, sealant, and coating applications may show blister formation upon cure. Blisters can be formed when carbon dioxide, generated in the reaction with isocyanate and water, is trapped in the film. This problem can be mitigated by employing latent hardeners such as blocked polyamines, which are activated upon moisture exposure. The hydrolysis of the latent hardener yields the polyamine that quickly reacts with the isocyanate, forming urea linkages, and then chain extends the polymer. The hydrolysis also releases the blocking agent, which can potentially create an unpleasant odor. In this work, a series of di- and trifunctional aldimines were synthesized from commercially available polyamines, biobased hydroxymethyl furfural, and lauroyl chloride. Hydroxymethyl furfural was first esterified with lauroyl chloride and subsequently condensed with the polyamines to form the aldimines. The application of these novel aldimines in a model moisture-curing system allowed the preparation of blister- and odor-free castings. Based on our results, the mechanical performance of the different aldimines in casting and adhesive applications could be related to the polymer network density. This was dependent on the rate of the aldimine hydrolysis reaction to produce the polyamine. In particular, the use of aldimines prepared from polyether amines and 1,5-diamino-2-methylpentane showed excellent adhesive properties.