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51.
A series of novel silicone modified polyurethane (Si-PU) surfactants were successfully synthesized by using hydroxypropyl-terminated polydimethylsiloxane (HPMS), polyethylene glycol (PEG), dimethylolpropionic acid (DMPA) and isophoronediisocyanate (IPDI). The chemical structure of the surfactant was confirmed by FTIR and 1H-NMR. TEM photographs showed that the micelles of the Si-PU surfactants dispersed in aqueous solution were spherical with the particle size in the range of 100–400 nm. Surface tension measurements indicated that these surfactants had low surface tension to 29.9 mN·m?1and a definite critical micelle concentration to, approximately 5.0×10?4–7.5×10?4mol·L?1. When the content of HPMS was 20 wt%, the surfactant's, emulsifying performance was superior to the traditionally available Span80/Tween80 mixed emulsifiers. In addition to that, no phase transition temperature was detected from 20°C to 90°C by fluorescence probe and DSC measurements, confirming the high thermal stability of the micelles.  相似文献   
52.
The bisazo chromophore molecule (CAAPM) and helical biphenyl bisazo polyurethane (HBBPU) were synthesized. The structures of CAAPM and HBBPU were characterized by FT-IR and UV-vis spectroscopic techniques. The measurements of refractive index and thermo-optic coefficient (dn/dT) of HBBPU were demonstrated at different wavelengths and different temperatures by the ATR technique. By using CCD digital imaging devices, transmission loss of the internal waveguide was measured. The refractive index dispersions and Sellmeyer coefficients of HBBPU were obtained by the Sellmeyer equation. A Y-branched switch based on the thermo-optic effect was proposed and the performance of the switch was simulated. With a branching angle of 0.143° and the FD-BPM method, the result showed that the power consumption of the thermo-optic switch could be only 3.6 mW, and the response time of the switch could reach about 8 ms. This is a significant improvement in reducing power consumption compared with the normal Y-branched polymer thermo-optic switch.  相似文献   
53.
通过一步法绿色合成了CdSe-聚氨酯(CdSe-PU)纳米复合发光材料.在N2保护下,将单质硒(Se)溶于蓖麻油,以蓖麻油酸作为氧化镉(CdO)的配体,合成硒化镉(CdSe)纳米晶.将聚丙二醇2000和异佛尔酮二异氰酸酯(IPDI)合成的预聚体,加入含CdSe纳米晶的蓖麻油溶液,通过交联作用得到CdSe-PU纳米复合发光材料.采用紫外-可见分光光度计(UV-Vis)、荧光光谱仪(PL)、傅里叶红外光谱仪(FT-IR)、热重分析仪(TGA)、透射电子显微镜(TEM)对CdSe纳米晶和聚氨酯复合材料的结构和性能进行了表征.结果表明:此方法合成的CdSe纳米晶性能良好,能在聚氨酯纳米复合材料中均匀分散且性能稳定,CdSe-PU纳米复合材料耐热性有所提高.  相似文献   
54.
A series of self-healable polyurethane (SHPU)/modified graphene (MG) nanocomposites were synthesized from poly(tetramethylene glycol) (PTMG) and 4,4′-methylene diphenyl diisocyanate (MDI) with minute amounts (0–1 wt%) of MG which was chemically modified graphene oxide (GO) with phenyl isocyanate and reduced in the presence of phenylhydrazine.  相似文献   
55.
The aqueous polyurethane hybrid dispersion modified by the epoxy resin were synthesized using 1,4-butanediol ( BDO ) and dimethylolpropionic(DMPA) as chain extenders. A kind of automobile interior decoration adhesive was made by the modified hybrid dispersions. Effects of the content and the kinds of epoxide resin on the properties of dispersions and dispersion-cast films such as appearance, pot life, viscosity, particle size, molecular mass, hardness, swelling in water, contact angle, strength of stress, elongation at break, and other mechanical properties were studied. At the same time the effect of the E20 content on the peel strength of the adhesive for several automobile interior decoration substrates such as rubber/wood, poly(vinyl chloride)/wood; leather/wood, sponge/wood was investigated. The experimental results show that when the epoxy resin E20 content was 8%, the modified polyurethane hybrid dispersions possess better properties and the adhesive made by the modified dispersions posses better adhesion for automobile interior decoration substrates. The stress-strain curve of the modified aqueous polyurethane hybrid dispersions films shows the modified aqueous cast films possess better rigidity and toughness.  相似文献   
56.
Dithiocarbamate modified polyurethane foam (DTC-PUF) was synthesized as a new solid-phase extraction sorbent for the preconcentration and determination of Fe(II), Mn(II) and Cu(II) in environmental samples using flame atomic absorption spectrometry. Maximum extraction of the elements was achieved at pH 5–7 and flow rate 3 mL min?1. Quantitative desorption was achieved by 10 mL from 1.0 mol L?1 HCl solution. The capacity of the sorbent was 149.2 ± 0.5, 237.5 ± 0.2, 200.2 ± 0.1 μg g?1 and the limit of detection was of 0.015, 0.015 and 0.012 μg mL?1for Fe(II), Mn(II) and Cu(II), respectively. A preconcentration factor of 100 was obtained for all elements. The developed method was successfully applied to the determination of the tested elements in water (tap and lake) and plant (spinach and parsley leaves) samples and showed good recovery values from 98 to 111% with corresponding RSD values ranged from 0.6 to 8.6%.  相似文献   
57.
A triol‐functional crosslinker combining the thermoreversible properties of Diels–Alder (DA) adducts in one molecule is designed, synthesized, and used as an ideal substitute of a traditional crosslinker to prepare thermal recyclable cross‐linked polyurethanes with excellent mechanical properties and recyclability in a very simple and efficient way. The recycle property of these materials achieved by the DA/retro‐DA reaction at a suitable temperature is verified by differential scanning calorimetry and in situ variable temperature solid‐state NMR experiments during the cyclic heating and cooling processes. The thermal recyclability and remending ability of the bulk polyurethanes is demonstrated by three polymer processing methods, including hot‐press molding, injection molding, and solution casting. It is notable that all the recycled cross‐linked polymers display nearly invariable elongation/stress at break compared to the as‐synthesized samples. Further end‐group functionalization of this single molecular DA crosslinker provides the potential in preparing a wide range of recyclable cross‐linked polymers.

  相似文献   

58.
采用生物质原料腰果酚和9,10-二氢-9-氧杂-10-膦杂菲-10-氧化物(DOPO)为原料, 合成了一种磷杂菲改性腰果酚多元醇(P-Cardanol-Polyol), 并利用核磁共振氢谱和磷谱对其结构进行了表征. 利用P-Cardanol-Polyol对聚氨酯硬泡(RPUF)进行阻燃改性, 得到一系列阻燃聚氨酯硬泡. 考察了P-Cardanol-Polyol的用量对阻燃聚氨酯硬泡的形貌、 密度、 热导率、 压缩性能、 热稳定性以及阻燃性能的影响. 研究结果表明, P-Cardanol-Polyol对聚氨酯硬泡的密度影响可以忽略不计; 随着P-Cardanol-Polyol的加入, 阻燃聚氨酯硬泡的平均孔径逐渐减小, 热导率也逐渐降低. 未改性聚氨酯硬泡的最大热释放速率和总放热量分别为390 kW/m2和31.9 MJ/m2, 阻燃聚氨酯硬泡则降低至340 kW/m2和24.6 MJ/m2. 此外, 阻燃聚氨酯硬泡的压缩强度比未改性聚氨酯硬泡提升了约13%. 炭层分析结果表明, P-Cardanol-Polyol能够促进聚氨酯硬泡形成连续致密且具有良好抗热氧化性能的炭层, 有利于减少燃烧过程中可燃性气体的逸出, 从而提升阻燃性能.  相似文献   
59.
A series of FR-RPUF composites were prepared by a one-step water foaming process with ammonium polyphosphate (APP) and steel slag (SS) as flame retardants. Thermogravimetric analysis (TG), limiting oxygen index (LOI), UL-94 vertical combustion test, microscale combustion calorimetry (MCC), TG-Fourier transform infrared spectrometry (TG-FTIR), scanning electron microscopy (SEM), Raman spectra and FTIR were used to investigate the thermal stability, flame retardancy, combustion performance, gas phase products, and char residue morphology of FR-RPUF composites. TG test results showed that the initial decomposition temperature (T-5wt%) and char residue rate at 700°C of RPUF/APP/SS composites were significantly enhanced by the addition of APP and SS, and the thermal stability of the composites was improved. Flame retardant test results confirmed the significantly increased LOI values of RPUF/APP/SS composites with V-0 rating. TG-FTIR also confirmed the obviously decreased release of toxic gases and flammable gases in the combustion of RPUF/APP/SS composites. SEM and Raman spectra of char residues for the composites suggested that APP/SS system improved the compactness and graphitization degree of char layer for RPUF/APP/SS composite. The above researches provide a new strategy for the utilization of SS in fire safety engineering.  相似文献   
60.
This study was focused on evaluating the suitability of a wide range of lignins, a natural polymer isolated from different plant sources and chemical extractions, in replacing 20 wt.% of petroleum-based polyol in the formulation of PU flexible foams. The main goal was to investigate the effect of unmodified lignin incorporation on the foam’s structural, mechanical, and thermal properties. The hydroxyl contents of the commercial lignins were measured using phosphorus nuclear magnetic resonance (31P NMR) spectroscopy, molar mass distributions with gel permeation chromatography (GPC), and thermal properties with differential scanning calorimetry (DSC) techniques. The results showed that incorporating 20 wt.% lignin increased tensile, compression, tear propagation strengths, thermal stability, and the support factor of the developed PU flexible foams. Additionally, statistical analysis of the results showed that foam properties such as density and compression force deflection were positively correlated with lignin’s total hydroxyl content. Studying correlations between lignin properties and the performance of the developed lignin-based PU foams showed that lignins with low hydroxyl content, high flexibility (low Tg), and high solubility in the co-polyol are better candidates for partially substituting petroleum-based polyols in the formulation of flexible PU foams intended for the automotive applications.  相似文献   
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