Modification of Nano-α-Al2O3 and Its Influence on the Surface Properties of Waterborne Polyurethane Resin Composite Passivation Films

Silane coupling agent KH560 was used to modify the surface of nano-α-Al2O3 in ethanol-aqueous solution with different proportions. The particle size of nano-α-Al2O3 was determined by nano-particle size analyzer, and the effects of nano-α-Al2O3 content, ethanol-aqueous solution ratio and KH560 dosage on the dispersion and particle size of nano-α-Al2O3 were investigated. The material structure before and after modification was determined by Fourier transform infrared spectroscopy (FTIR). Aqueous polyurethane resin and inorganic components are combined with modified nano-α-Al2O3 dispersion to form chromium-free passivation solution. The solution is coated on the galvanized sheet, the adhesion and surface hardness are tested, the bonding strength of the coating and the surface hardness of the substrate are discussed. The corrosion resistance and surface morphology of the matrix were investigated by electrochemical test, neutral salt spray test and scanning electron microscope test. The chromium-free passivation film formed after the modification of nano-α-Al2O3 increases the surface hardness of galvanized sheet by about 85%. The corrosion resistance of the film is better than that of a single polyurethane film. The results show that the surface hardness and corrosion resistance of polyurethane resin composite passivation film are significantly improved by the introduction of nano-α-Al2O3.

Application of Water-Based Polyurethane in Sunscreen Products

With the development of the economy and improving quality of life,sunscreen products have become an indispensable part of people’s daily lives.However,traditional sunscreen products have several shortcomings,such as sticky skin feel,clumping,and skin irritation.In addition,the price of sunscreen products is relatively high due to the expensive ingredient:UV absorbers.To solve the above problems,a film-forming agent had been added to the general sunscreen formula to synergistically improve the consumer experience without causing any adverse side effects.It is crucial to achieve sun protection factors(SPF)booster through other cheaper agents.This article mainly studies and verifies the synergistic impact of Carfil■UV35(a water-based polyurethane product)in sunscreen products and discusses its application scope.The hen’s eggchorioallantoic membrane assay(HET-CAM)test and the human patch test were used to verify its mildness to the skin.Results also showed that Carfil■UV35 could effectively improve the water resistance of sunscreen products.What’s more,the SPF improvement test shows that only 5% Carfil■UV35 can increase the SPF value from 15 to 30.In short,the research in this article can provide specific ideas for the formulation design of sunscreen products and is of great significance to the application and SPF increase of water-based polyurethane film-forming agents in sunscreen cosmetics.

STUDY ON HYDROLYSIS RESISTANT POLYCARBONATE POLYURETHANE EPOXY RESIN BLENDS

This paper studies the structure and properties of the polycarbonate polyurethane epoxy resin (PCPU EP) blends being resistant to hydrolysis.The samples were analyzed by an infrared spectrometer,a differential scanning calorimeter,a scanning electron microscope and a dynamic viscoelastometer.The results show that PCPU EP blends have excellent resistance to hydrolysis and mechanical properties at the ratio of PCPU to EP equal to 10/100 (wt/wt).

Preparation and Characterization of Two-component Waterborne Polyurethane Comprised of Water-soluble Acrylic Resin and HDI Biuret

A two-component waterborne polyurethane(2K-WPU) was prepared by mixing water-soluble acrylic resin and hexamethylene diisocyanate biuret, and then diluted for phase inversion with water. Compared with water-soluble acrylic resin, the phase inversion of 2K-WPU occurs at lower water content. It is indicated by TEM that 2K-WPU parti-cles show a core-shell structure, in which HDI biuret is encapsulated by hydrophilic acrylic resin. 2K-WPU emulsion with HDI biuret has larger particle size and narrower distribution index, while for 2K-WPU emulsion with HDI iso-cyanurate, the latex not only has large particle size, but also has two-peak distribution. FTIR shows that the reaction be-tween HDI biuret and acrylic resin can complete in 12h. In addition, studies on effect of composition of acrylic resin on performance of 2K-WPU show that narrowing the polar difference between water-soluble acrylic resin and HDI biuret and improving the miscibility of two components are the key to prepare the transparent and high gloss films with high crosslinking density.

Preparation, morphology and mechanical properties of acrylate-modified polyurethane/unsaturated polyester resin graft-IPNs

Acrylate modified polyurethane resin was first synthesized, and interpenetrated with unsaturated polyester resin to form IPNs and gradient IPNs which cured at room temperature. The polymerization process was traced by an IR spectroscopy technique and the simultaneous interpenetrating techniques were determined. The morphology of these IPNs were estimated by TMA and TEM methods. The results indicated that large amount of interpenetrating and entanglement make T g linked up effectively, and domains between two phases can be in nanometre ranges, which changed with composition ratios. The mechanical properties results showed that IPNs varied from elastomeric to plastic materials. It was noteworthy that, with the introduction of modified groups and the formation of graft construction in IPNs, the miscibility in the systems was improved a lot. These further led to the improved mechanical properties of IPNs with elastomer reinforced and plasticizer toughened as well. The reinforced miscibility between the networks can apparently change mechanical property especially for the gradient ones when the materials are elongated.

DynamicMechanical and Chemorheology Analysis for the Blended Epoxy System with Polyurethane Modified Resin

As the important matrix material,epoxy resin has been widely used in the composites for various fields.On account of the poor toughness of epoxy resin limiting their suitability for advanced applications,considerable interests have been conducted to modify the epoxy resin to meet the engineering requirements.In this study,the bio-based polyurethane(PU)modified resin was adopted to modify the pure bisphenol-A epoxy by blending method with various proportions.Aiming to illuminate the curing behavior,mechanical and thermal properties,the blended epoxy systems were characterized by viscosity-time analysis,dynamic mechanical analysis(DMA)at different frequencies and temperatures,mechanical tensile test,thermogravimetric analysis(TGA)and Fourier transform infrared(FT-IR)spectroscopy.The results indicated that the introduction of PU modified epoxy was found to significantly inhibit the viscosity growth rates especially when the content of PU modified epoxy resin is higher than 60%.Notwithstanding the dynamic modulus and T_(g)reduced with the increment of PU modified epoxy,remarkable increment on the elongation at break was found and the flexibility was greatly promoted with the introduction of PU modified epoxy.The proportion of PU modified epoxy in the blends should be put balance considerations to obtain optimal mechanical properties.TGA results and FTIR spectrum demonstrated that the addition of PU modified epoxy did not change the thermal decomposition mechanism and chemical reaction mechanism,but the addition of PU modified epoxy inhibits the curing reaction of epoxy resin by measured and calculated the damping temperature domain
T from 35.7℃ to 48.9℃.

Synthesis and Performance of Transparent Casting Polyurethane Resin

A series of transparent casting polyurethane resins (TCPU) were synthesized from cycloaliphatic diisocyanate (IPDI or H_(12)MDI), polyol, chain extender, crosslinking agents, catalyst and special aids (T),which were characterized by FTIR. The thermal stabilities of the obtained TCPU were examined by DSC and TGA, the glass transition temperature (T_g) was in the range of 95-110 ℃, the initial decomposition temperature (5% weight loss) was 250-265 ℃, and 10% weight loss at the temperature was in the range of 260-286℃ in nitrogen atmosphere. The morphologies of the fractured surfaces of TCPU were revealed by a scanning electron microscope (SEM). The crystalline-amorphous characters of TCPU were studied by WAXD, the result shows that TCPU possesses amorphous glassy characters. The optical properties of TCPU were studied by a UV-7500 visible light absorbance measurement. All the samples exhibited excellent optical properties and possessed light transmittance in the range of 91%-93%.

Curing mechanism of TDE-85/MeTHPA epoxy resin modified by polyurethane

Diglycidyl 4,5-epoxy tetrahydro phthalate/methyl tetrahydrophthalic anhydride （TDE-85/MeTHPA） epoxy resin modified by polyurethane （PU） was prepared with 1,4-butanediol （1,4-BDO）, trimethylol propane （TMP） and polyurethane prepolymer synthesized by polypropylene glycol and toluene diisocynate. Chemical reaction and curing mechanism of this system were discussed by incorporating the results of infra spectrum analysis. The results indicate that the epoxy polymeric network I is obtained by the curing reaction between TDE-85 and MeTHPA, while the PU polymeric network II is obtained by the chain-extended and crosslinking reaction between 1,4-BDO, TMP and polyurethane prepolymer（PUP）. The graft chemical bonds are formed between polymer networks I and II that therefore increase the degree of blend and compatibility between epoxy polymer and PU.

Structural characteristics and properties of polyurethane modified TDE-85/MeTHPA epoxy resin with interpenetrating polymer networks

Diglycidyl-4,5-epoxycyclohexane-1,2-dicarboxylate(TDE-85)/methyl tetrahydrophthalic anhydride (MeTHPA) epoxy resin was modified with polyurethane(PU) and the interpenetrating polymer networks(IPNs) of PU-modified TDE-85/MeTHPA resin were prepared. The structural characteristics and properties of PU-modified TDE-85/MeTHPA resin were investigated by Fourier transform infrared(FTIR) spectrum,emission scanning electron microscopy(SEM) and thermogravimetry(TG). The results indicate that epoxy polymer network (Ⅰ) and polyurethane polymer network (Ⅱ) of the modified resin can be obtained and the networks (Ⅰ) and (Ⅱ) interpenetrate and tangle highly each other at the phase interface. The micro morphology presents heterogeneous structure. The integrative properties of PU-modified TDE-85/MeTHPA epoxy resin are improved obviously. The PU-modified TDE-85/ MeTHPA resin's tensile strength reaches 69.39 MPa,the impact strength reaches 23.56 kJ/m,the temperature for the system to lose 1% mass (t1%) is 300 ℃,and that for the system to lose 50% mass (t50%) is 378 ℃. Compared with those of TDE-85/MeTHPA resin,the tensile strength,impact strength,t1% and t50% of the PU-modified resin increases by 48%,115%,30 ℃,11 ℃,respectively. The PU-modified TDE-85/MeTHPA resin has the structure characteristics and properties of interpenetrating polymer networks.

Synthesis and Characterization of Polyurethane and Epoxy Resin Interpenetrating Polymer Network

A series of Polyurethane (PU)/bisphenol A based Epoxy Resin(EP) Interpenetrating Polymer Networks(IPN) were synthesized and characterized by SEM, DSC, TGA and DMTA. It was found that IPN shows the best compatibility and damping properties when the ratio of PU/EP is 80 to 20. The results show that chain-extender and higher molecular weight of PPG are able to improve the properties of compatibility, damping and thermal properties.

Application of reactive acrylate microgels in water-base coatings

Reactive acrylate microgels with different reactive groups such as carboxyl, hydroxide groups had excellent properties such as quick-dry, low viscosity, high adhesion and hardness, which made them extensively used in preparing paints or in coating-modification. Reactive acrylate microgels were prepared by emulsion co-polymerization with zwitterions surfactant, anionic surfactant and nonionic surfactant as co-emulsifier. The water-base baking paints made from reactive acrylate microgels and melamine-formaldehyde resin had excellent combination properties. The aluminium powder can be well-dispersed in the paints. The influences of monomer components on the properties of the water-base baking paints were discussed in this paper. And the baking paints were also compared with the marketing solvent acrylate baking paints. It was found that the water-base acrylate amino baking paints had better combination properties than the organic solvent acrylate baking paints, which means that the water-base baking paints had a bright marketing future.

水利工程用环氧树脂改性聚氨酯丙烯酸酯性能研究

水利工程金属结构和水工建筑物常遭受腐蚀、高速含沙水流磨蚀破坏,需对其进行便捷有效的防护。利用环氧树脂对聚氨酯丙烯酸酯(PUA)进行改性提高PUA与基体黏结性能,采用紫外光(UV)固化技术制备PUA涂层。研究了环氧树脂改性PUA的化学结构及环氧树脂用量对PUA的力学性能、热稳定性能、耐溶剂性能和抗冲磨性能的影响。结果表明,环氧树脂改性PUA的拉伸强度随着环氧树脂用量增加,呈下降趋势,当加入5%时,PUA拉伸强度为103.0 MPa,材料呈强而脆的特性。环氧树脂加入提升了PUA的拉伸剪切强度,由0.25 MPa增至1.60 MPa。同时,环氧树脂改性PUA具有良好的耐水性能、耐溶剂性能、抗冲磨性能,5%环氧树脂改性PUA抗冲磨强度为800 h/(kg·m^(2))。

聚氨酯和环氧树脂涂层耐水性能对比研究

本文选择了不同类型的聚氨酯(PU)涂层和环氧树脂(EP)涂层作为代表,通过红外光谱、固态核磁共振、热失重分析和热力学性能分析,研究了长期水下浸泡对涂层结构和性能的影响,并进一步对比了上述不同材料的水解稳定性。结果表明,聚醚型聚氨酯(PTMG-PU)涂层具有最优的耐水性,并且其化学结构基本没发生化学水解作用,然而加入陶瓷增强颗粒会降低材料的耐水性,并可能加速水解作用对涂层结构和性能的影响;相同水解条件下,聚酯型聚氨酯(PEA-PU)和EP涂层在水中的耐水性较差,并且可能发生聚合物链的化学水解作用,进而导致材料储能模量的提高。

塑胶跑道用超细纤维聚氨酯合成革的制备及性能测试

为改善塑胶跑道综合应用性能,优化超细纤维聚氨酯合成革物理机械性能,本文由聚氨酯树脂含浸无纺布制备了超细纤维聚氨酯合成革,并对其力学性能与卫生性能进行了测试表征。结果发现,随着聚氨酯浸渍率增加,超细纤维聚氨酯合成革基布表观密度增大,密实程度提高,而压缩弹性率先增加后减少;随着聚氨酯浸渍率增加,超细纤维聚氨酯合成革基布剥离强度逐渐升高,拉伸强度、断裂伸长率皆呈现先降低后升高再降低的曲线形态,而撕裂强度则表现为先降低后升高的态势;随着聚氨酯浸渍率增加,超细纤维聚氨酯合成革基布透气性与透水汽性持续性下降;超细纤维聚氨酯合成革基布的干擦与湿擦色牢度均可达到5,而于氢氧化钠溶液中不溶色,表明基布耐碱性良好。

超细纤维合成革透水汽性能的研究进展

超细纤维合成革(简称超纤革)是替代天然皮革的理想材料,但超纤革的透水汽性能与天然皮革相比仍存在差距,有待提升。文章概述了超纤革的制备过程,分析了超纤革的性能及其在透水汽性能方面的不足,并从超纤革的主要组分,即超纤革基布和聚氨酯树脂入手,探讨了超纤革透水汽性能研究的最新进展;总结了对超纤革基布的水解、增加活性基团和亲水剂等改性方法,阐述了对聚氨酯树脂的填料、接枝聚合和共混等改性措施,探讨了对超纤革的后整理改性选项,最后提出了超纤革透水汽性能研究的未来发展方向。

热塑性树脂增韧环氧树脂复合材料研究进展

为了解决环氧树脂固化导致严重脆弱,低韧性和恶劣的内冲击性缺点,在特定范围内限制适用的问题,本文通过整理近年来环氧树脂增韧的相关文献,研究了热塑性树脂的改性方法和改性后界面情况的进展,对聚砜、聚醚砜、聚醚醚酮、聚酰亚胺等热塑性树脂增韧环氧树脂研究现状进行了分析。研究发现:热塑性树脂增韧环氧树脂的共混体系从均相状态到高交联结构的固定相形态,这种转变极大程度提高了材料的性能。

水性丙烯酸涂层改性研究进展

简单阐述了水性丙烯酸树脂的单体结构、聚合方法以及应用现状;较为系统地总结了根据不同材料改性水性丙烯酸树脂的研究进展,改性材料可归纳为纳米材料、有机硅、有机氟、聚氨酯和环氧树脂以及一些新型材料等。重点论述了改性材料对水性丙烯酸树脂进行改性的反应机理、相应的微观结构及性能提高情况。展望了水性丙烯酸涂料发展的方向。

环氧树脂-改性聚氨酯及聚脲复合涂层的制备及防护性能研究

为了解决传统防护涂层材料单一、防护性能难以兼顾,单组分多元醇制备聚氨酯分子结构存在缺陷、聚脲固化速率过快的问题,通过改变聚氨酯合成原料中PTMG2000和聚醚3050的混合比例来调控聚氨酯交联、微相分离程度以改进其性能,同时采用P1000与扩链剂MDBA来制备可手工涂覆的慢反应聚脲,将环氧树脂作为底漆、聚氨酯-聚脲作为面漆,制备了一种具有优良耐磨、防腐、抗冲击等防护性能的涂层。结果表明:当m(PTMG2000)∶m(聚醚3050)=1∶2时制备的聚氨酯与PU-3050相比,其拉伸强度为13.19 MPa,提高了85.25%,伸长率为289.14%,提高了140%,热分解50%的温度从392.45℃提高到400.28℃,水接触角从90.72°增大到98.29°,综合性能得到提升。复合涂层在15 d中性盐雾测试后涂层未起泡、锈蚀面积小,高于ISO 9227-2006标准要求;附着力为0级,高于ISO 2409-2007标准要求的3级;抗冲击强度为100 cm,高于GB/T 1732-2020标准指定的最高50 cm冲击强度;在3.5%NaCl溶液中腐蚀9 d后阻抗维持在4.245×10^(7)Ω·cm^(2),30 min磨损量为10.28 mg,防护性能优异。

树脂基高吸油材料的研究进展

从树脂基材料吸油机理着手,介绍了树脂基泡沫和丙烯酸树脂等吸油材料近几年的国内外研究动态。最后,总结了研究中存在的问题,并展望了吸油材料未来的发展走向。