制备工艺对聚氨酯酰亚胺泡沫性能的影响

以均苯四甲酸二酐(PMDA)、多苯基多亚甲基多异氰酸酯(PAPI)、聚醚多元醇为主要原料,分别采用聚酰亚胺(PI)预聚法、聚氨酯(PU)预聚法和一步法制备聚氨酯酰亚胺泡沫,从微观形貌、力学性能、热稳定性能以及阻燃性能方面对上述3种制备工艺进行对比和评估。实验结果表明,采用一步法制备PUI泡沫时,PU链段和PI链段同时增长,容易造成泡孔缺陷,导致泡沫的力学性能较差;在采用PU预聚法制备的PUI泡沫中,PU链段含量较高,因此,泡孔孔径分布较宽且平均泡孔直径较大,对应的热稳定性和阻燃性能较差;采用PI预聚法制备的PUI泡沫的泡孔孔径分布窄且平均泡孔直径较小,对应的压缩性能、热稳定性以及阻燃性能均达到最佳。     

Fabrication of multi-filler thermoset-based composite bipolar plates for PEMFCs applications: Molding defects and properties characterizations

The bipolar plate (BP) material should possess contradictory properties. They should also manufacture from low-cost methods and materials. In the current investigation, thermoset-based composite materials reinforced with conductive fillers, and the compression molding process is implemented. In addition to fabricating the bipolar plates (BPs) with and without the flowing channels, alleviating the defects during the molding process is performed. The channels are perfectly formed on the plates with the designed depth of 0.65 mm and 0.5 mm of width. In the meanwhile, we alleviate different molding defects, which spoil the surface appearance and part properties. Regarding the physical properties, the water contact angle is measured to be around 85°. The through-plane electrical conductivity of molded plates showed high values up to 38 S/cm, and the interfacial contact resistance measured to be 18–24 mΩ cm². The mean value of the flexural strength of the produced samples was equal to 47 MPa, which is almost twice the DOE target (>25 MPa).     

Effect of shock structure on stabilization and blow-off of hydrogen jet flames

Under-expanded hydrogen jet has characteristic shock structure immediately downstream of the nozzle exit. The shock structure depends on the ratio p_EX/p_A, i.e. the ratio of nozzle exit to ambient pressure, and the distributions of velocity and concentration in an under-expanded hydrogen jet depend on characteristics of the shock structure. Therefore, the shock structure should affect the blow-off behaviour of under-expanded hydrogen jet flame. Since this issue has not been investigated in detail, this study aims to close this knowledge gap. The effect of changes in shock structure on lift-off length and blow-off conditions for non-premixed turbulent hydrogen free jet flame has been experimentally investigated. The shock structure was varied by using three types of nozzles: convergent, straight and divergent nozzles. Inlet diameters of nozzles change from 0.31 to 1.04 mm and outlet diameters from 0.34 to 1.7 mm. The static pressure and the ratio of cross-section area at the nozzle inlet to that at the outlet were varying parameters in this study. Hydrogen was horizontally spouted through a nozzle to atmosphere. The maximum static pressure in a nozzle was 13.2 MPa. The experiments revealed that when the hydrogen jet had sequential shock cell structures, which occurred in the range of p_EX/p_A smaller than 2.45, a higher mass flow rate of hydrogen was needed for the stabilization of a jet flame than that for p_EX/p_A larger than 2.45 and that when closed to the ideal expansion (p_EX/p_A = 1), the mass flow rate for stable flame became maximum. In addition, it was observed that the lift-off length of stable flames followed with sequential shock cell structures were almost the same when the minimum cross-section area of used nozzles was constant. However, when hydrogen jet had a shock structure with single Mach disk, the lift-off lengths and the minimum mass flow rate required for the stable jet flame were decreasing with the decrease of the cross-sectional area ratio of the nozzle exit to inlet.     

Chloride migration in concrete with superabsorbent polymers

Superabsorbent polymers (SAP) can be used as a means for internal curing of concrete. In the present study, the development of transport properties of concrete with SAP is investigated. The chloride migration coefficient according to NT BUILD 492 is used as a measure of this. Twenty concrete mixtures are tested 7, 14, and 28 days after casting. The development of degree of hydration is followed for 20 corresponding paste mixtures.Both when SAP is added with extra water to compensate the SAP water absorption in fresh concrete and without extra water, the internal curing water held by SAP may contribute to increase the degree of hydration. No matter if SAP is added with or without extra water, it appears that the so-called gel space ratio can be used as a key parameter to link age and mixture proportions (water-to-cement ratio and SAP dosage) to the resulting chloride migration coefficient; the higher the volume of gel solid relative to the space available for it, the lower the chloride migration coefficient, because the pore system becomes more tortuous and the porosity becomes less.     

New semi-conducting poly(phenylene vinylene-alt-anthrylene vinylene)s: Synthesis,characterization and photophysical properties

An anthracene-based semi-conducting polymer (P1) and its cyano-analogue (P2) were synthesized via the Wittig and Knoevenagel polycondensations. The polymers were soluble in common organic solvents and have number-average molecular weights of 13,750 and 6430 g mol⁻¹ for P1 and P2, respectively. The DSC analyzes show a good thermal stability and an amorphous morphology in solid state for these organic materials. The optical properties of the polymers were investigated by UV–visible absorption and fluorescence spectroscopies. The HOMO and LUMO levels were estimated using cyclic voltammetry analysis. The effect of cyano group on the photophysical properties of poly(phenylene vinylene-alt-anthrylene vinylene)s was investigated. The results demonstrate an enhancement in the ionization potential and a significant improvement of the fluorescence yield due to introduction of such groups into the π-conjugated system. Single-layer diodes based on these organic semiconductors have been fabricated and showed relatively low turn-on voltages.     

Improvement in flame retardancy of polyurethane dispersions by newer reactive flame retardant

A novel phosphorus containing reactive flame retardant was synthesized and incorporated successfully in polyurethane backbone to obtain flame retardant aqueous polyurethane dispersions (FRPUDs). The reactive flame retardant compound was synthesized by using phosphorus oxychloride (1 mole) and N-methylaminoethanol (3 mole). The structure of synthesized phosphorus containing triol was confirmed by FTIR, ¹H NMR and ³¹P NMR spectrometry. Further, polyurethane prepolymer was modified with phosphorus containing triol compound in various amounts (30, 40 and 50% on equivalent basis) and FRPUDs were prepared. PUD films were applied on wood and mild steel panels and air dried. It was then characterized for mechanical, chemical, thermal and flame retardant properties. It was observed that all FRPUDs exhibited good mechanical properties and improved flame retardancy as compared to the conventional one. The maximum limiting oxygen index (LOI) value of 37 was obtained for FRPUD containing 0.8 mass% of phosphorus and 1 mass% of nitrogen. The flame retardancy was greatly depending on the phosphorus content and increased with increase in phosphorus content.     

Studying the effect of organo-modified nanoclay loading on the thermal stability,flame retardant,anti-corrosive and mechanical properties of polyurethane nanocomposite for surface coating

Clay polyurethane nanocomposite (CPN) coating films were fabricated by uniformly dispersing nanoclay, organically modified with 25–30 wt.% octadecylamine in varying concentrations up to 5 wt.%, in a commercial two component, glossy, acrylic aliphatic polyurethane using ultrasonication. Organo-modified nanoclay was characterized by X-ray diffraction (XRD). The dispersion of the nanoclay into the matrix was investigated by scanning electron microscopy (SEM). CPN coating films were characterized by thermogravimetric analysis (TGA), and flame retardant, corrosion resistance and mechanical properties were also investigated. The XRD measurement indicated that, the organo-modified nanoclay particles were mainly constituted of montmorillonite with traces of quartz and calcite also found to be present. The SEM analysis showed that the nanoclay layers were dispersed and intercalated into the polyurethane coating. Thermogravimetric analysis showed that incorporating 5 wt.% organo-nanoclay into polyurethane considerably enhanced the thermal stability and increased the char residue to 14.11 wt.% relative to 4.58 for the sample without organo-nanoclay (blank polyurethane). The limiting oxygen index (LOI) test revealed that incorporation of organo-nanoclay led to a further increase in LOI values, which indicate an improvement in flame retardancy properties. The corrosion resistance also improved and this improvement increases with increase nanoclay wt.%. The mechanical resistance measurements demonstrated that the gloss of the CPN coating films slightly decreased, although hardness, adhesion and impact resistance of the CPN coating films improved with the incorporation of the organo-nanoclay.     

Different chemical effect of hydrogen addition on soot formation in laminar coflow methane and ethylene diffusion flames

Previous studies showed that adding hydrogen (H₂) can have an opposite chemical effect on soot formation: its chemical effect enhances and suppresses soot formation in methane (CH₄) and ethylene (C₂H₄) diffusion flames, respectively. Such opposite chemical effect of H₂ (CE-H₂) remains unresolved. The different CE-H₂ is studied numerically in the two laminar coflow diffusion flames. A detailed chemical mechanism with the addition of a chemically inert virtual species FH₂ is used to model the gas-phase combustion chemistry in this study. Particularly, a reaction pathway analysis was performed based on the numerical results to gain insights into how H₂ addition to fuel affects the pathways leading to the formation of benzene (A₁) in CH₄ and C₂H₄ flames. The numerical results show that the CE-H₂ in CH₄ diffusion flame to prompt soot formation is ascribed that the higher mole fraction of H atom promotes the formation of A₁ and Acetylene (C₂H₂) and leads to higher nucleation rate and eventually higher soot surface growth rate. In contrast, adding H₂ to C₂H₄ diffusion flames decreases soot nucleation and surface growth rate. The lower soot nucleation rate is due to the lower mole fractions of pyrene (A₄), while the lower soot surface growth rate is due to the lower mole fractions of H atom and C₂H₂, higher mole fraction of H₂ and lower soot nucleation rate. Furthermore, the CE-H₂ in C₂H₄ diffusion flames promotes the formation of A₁, but suppresses the formation of A₄.     

Highly stretchable self-sensing actuator based on conductive photothermally-responsive hydrogel

Soft robots built with active soft materials have been increasingly attractive. Despite tremendous efforts in soft sensors and actuators, it remains extremely challenging to construct intelligent soft materials that simultaneously actuate and sense their own motions, resembling living organisms’ neuromuscular behaviors. This work presents a soft robotic strategy that couples actuation and strain-sensing into a single homogeneous material, composed of an interpenetrating double-network of a nanostructured thermo-responsive hydrogel poly(N-isopropylacrylamide) (PNIPAAm) and a light-absorbing, electrically conductive polymer polypyrrole (PPy). This design grants the material both photo/thermal-responsiveness and piezoresistive-responsiveness, enabling remotely-triggered actuation and local strain-sensing. This self-sensing actuating soft material demonstrated ultra-high stretchability (210%) and large volume shrinkage (70%) rapidly upon irradiation or heating (13%/°C, 6-time faster than conventional PNIPAAm). The significant deswelling of the hydrogel network induces densification of percolation in the PPy network, leading to a drastic conductivity change upon locomotion with a gauge factor of 1.0. The material demonstrated a variety of precise and remotely-driven photo-responsive locomotion such as signal-tracking, bending, weightlifting, object grasping and transporting, while simultaneously monitoring these motions itself via real-time resistance change. The multifunctional sensory actuatable materials may lead to the next-generation soft robots of higher levels of autonomy and complexity with self-diagnostic feedback control.     

A facile method for preparation of PGS@ZB‐N and gas‐sol alternating synergistic effect for fire resistance of EVA

Through the simple precipitation of palygorskite (PGS) by zinc borate (ZB) (to make PGS@ZB) and the decoration of PGS@ZB by dodecylamine (N), a novel organic‐inorganic@inorganic hybrid flame retardant of PGS@ZB‐N was prepared and was incorporated with ethylene vinyl acetate copolymer (EVA) to improve its flame retardance. The structure and morphology of PGS@ZB‐N were characterized by Fourier transform infrared (FTIR) spectroscopy, X‐ray diffraction (XRD), and scanning electron microscopy (SEM), and it was confirmed that the PGS@ZB‐N hybrid had been successfully prepared. The flame retardancy and burning behavior of EVA/PGS@ZB‐N/EG (EG = expandable graphite) composite were studied through thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL‐94 (by the vertical burning test), and cone calorimeter test (CCT) characterizations. The prepared EVA/PGS@ZB‐N/EG composite obtained an LOI value of 41.2% with the addition of 30 wt% PGS@ZB‐N/EG. It was found that EVA/PGS@ZB‐N/EG was protected through a gas phase and condensed phase alternating synergistic effect mechanism.