无卤无机阻燃剂最佳配方的研究

LDPE无卤无机阻燃是当前塑料材料的重要研究方向。通过实验研究当LDPE中加入Al（OH）3、Mg（OH）2、红磷、硼酸锌（ZB）等无卤无机阻燃剂的单一体系和复配体系后对LDPE阻燃性能、力学性能及流动性能的影响,从而研制出阻燃剂的最佳配方。     

硼-磷-氮协效膨胀型阻燃剂的合成与性能研究

以三聚氰胺(MEL)、磷酸(PA)、硼酸(BA)等为原料,合成了三聚氰胺磷酸盐(MP)和三聚氰胺硼酸盐(MB)中间体,以及三聚氰胺磷酸硼酸盐(MPB)硼-磷-氮协效三位一体膨胀型阻燃剂,用红外光谱和元素分析等方法对合成产物的结构和组成进行了表征,确定了阻燃剂合成的最佳条件。探讨了MPB的元素组成对MPB阻燃环氧树脂复合材料氧指数的影响,以及MPB的协同阻燃机理。结果表明:合成MP时,三聚氰胺和磷酸的最佳摩尔比为1:0.5;合成MB时,三聚氰胺和硼酸的最佳摩尔比为10:1;合成MPB-1(以MP为中间体)的最佳质量比为w(MP):w(BA)=3:1;合成MPB-2(以MB为中间体)的最佳质量比为w(MB):w(PA)=0.92:1。MPB-2对环氧树脂的阻燃性能优于MPB-1,这是由于MPB-2中元素组成均衡,使得B-P-N协效作用明显。     

埃洛石对水性超薄膨胀型钢结构防火涂料防火性能的影响

以聚丙烯酸酯乳液为基体树脂,多聚磷酸铵、三聚氰胺、季戊四醇等为主阻燃剂,埃洛石纳米管(HNTs)为阻燃协效剂,制备了水性超薄膨胀型钢结构防火涂料,采用模拟大板燃烧法和锥形量热仪对其耐火性能进行了研究,并用扫描电镜观察了膨胀炭层的表面形貌。结果表明:HNTs对防火涂料的耐火性能影响显著,当阻燃体系中HNTs含量为10.86%时,HNTs与主阻燃剂之间有阻燃增效作用,所制备防火涂料的耐火时间为107 min,点燃时间为24 s,热释放速率峰值与点燃时间比为4.97,燃烧残余量高达48.36%,且燃烧残余物表面致密,显示出优异的耐火性能。     

壳寡糖对Q235钢在海水中的缓蚀性能

采用腐蚀浸泡试验,扫描电子显微镜以及电化学试验法等研究了海水中壳寡糖(COS)及其与无机缓蚀剂复配后对Q235钢的缓蚀作用。电化学试验结果表明:单独添加COS时,缓蚀率最大为65.73%;当COS与NaNO_2复配添加时,其协同缓蚀率为90.67%,为阳极型缓蚀剂;而当COS与Na_2MoO_4复配时,缓蚀率最大只能达到71.65%,且两者发生了抑制作用。腐蚀浸泡试验结果表明:当COS与NaNO_2复配使用时,其缓蚀率最佳,为85.90%。COS在Q235钢表面发生单分子吸附,为自发进行的化学吸附,从而起到缓蚀作用,该吸附符合Langmuir模型。     

Composite corrosion inhibitors for secondary alkaline zinc anodes

The corrosion inhibition property of PEG600 and In(OH)3 as composite corrosion inhibitors for secondary alkaline zinc electrodes was studied, and the inhibition efficiency was determined as 81.9%. The research focused on the mechanism by the methods of electrochemical impedance spectroscopy, polarization curves and IR spectroscopy. The results indicate that the corrosion inhibition effectiveness is attributed to the joint inhibition of anodic zinc dissolution and cathodic hydrogen evolution. And the anodic process is depressed to a greater extent than the cathodic process. The synergistic mechanism of the composite inhinbitors proves to be the enhancement of adsorption of PEG600 by In(OH)3. Potentiostatic experiment results and SEM images verify the inhibition of dendritic growth by the composite inhibitors.     

316L不锈钢微动磨蚀过程力学化学交互作用研究

采用球－平面接触微动设备,对３１６Ｌ不锈钢在不同ＮａＣｌ溶液中微动过程力学化学交互作用进行了研究,并解析了材料微动损伤速率与溶液腐蚀特性之间的关系。结果表明,材料微动过程力学化学作用相互促进,力学损伤在微动损伤过程中占居主导作用。强碱性、强酸性及溶液富含Ｃｌ＾－的情况下,都可导致材料严重微动损伤,而在中性条件下,力学因素对化学损伤促进作用最为明显。     

Synergistic effects of organically modified montmorillonite in combination with metal oxides on the fire safety enhancement of intumescent flame-retarded epoxy resins

Synergistic effects of organically modified montmorillonite (OMMT) in combination with different metal oxides (Bi₂O₃, Sb₂O₃, and MoO₃) on the fire safety enhancement of the intumescent flame-retarded epoxy resins (EPs) were systematically evaluated. The results from X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses show that the OMMT and metal oxides acquire a uniform distribution in the EP matrix, and OMMT platelets exhibit a fully exfoliated state. The flammability and thermogravimetry (TG) tests show that the intumescent flame retardant (IFR)-OMMT-metal oxide ternary system can endow EPs with the higher synergistic efficiencies on the enhancement of flame retardancy, smoke suppression properties, and charring ability compared to those of IFR or IFR-OMMT system, and the synergistic efficiency is the following order: IFR/OMMT/Sb₂O₃ > IFR/OMMT/MoO₃ > IFR/OMMT/Bi₂O₃. In particular, the sample, filled with 1.5 wt% OMMT, 1.5 wt% Sb₂O₃, and 27 wt% IFR, passes the UL94 V-0 rating and acquires the highest limiting oxygen index value of 28.5% among the samples. The IFR-OMMT-metal oxide ternary system exerts a better synergistic effect on the generation of crosslinking and aromatic structures that supply the excellent charring effect and barrier effect for the EPs, and the synergistic efficiency of IFR-OMMT-metal oxide ternary system is varied with the types of metal oxides.     

Preparation and performance of waterborne polyurethane coatings based on the synergistic flame retardant of ferrocene,phosphorus and nitrogen

A synergistic reactive flame-retardant polyol (AFeDH) containing ferrocene, phosphorus, and nitrogen elements was synthesized from ferro-formaldehyde, 5-amino-1,3, 4-thiadiazole-2-mercaptan, 9,10-dihydro-9-oxa-10-phos-phaphenanthrene-10-oxide and hydroxyl terminated polybutadiene acrylonitrile, and then applied for flame retarding waterborne polyurethane (WPU). The chemical structures of intermediates and final products were well characterized to confirm the successful preparation of ternary P-N-Fe flame retardant. The effects of incorporated AFeDH on thermal stability, flame retardancy and mechanical properties of AFeDH/WPU films were systematically studied. The results indicated that LOI value increased with the increase amount of AFeDH, while the value then decreased as the loading content above 6 wt%. This increase in flame retardancy results from the competition between the catalytic degradation of iron and the catalytic carbonization. Benefiting from the good synergistic effects among each element of AFeDH, the WPU/AFeDH films perform the decreased heat release and smoke production. Moreover, the flame retardant films also show the enhanced tensile strength of 33.8 MPa and elongation at break of 763.3%. Therefore, this novel halogen-free flame retardant shows an excellent synergistic effect among P, N, and Fe elements, which has a great potential in the application of flame retardant WPU.     

Covalent Linkage and Macrocylization Preserve and Enhance Synergistic Interactions in Catalytic Amyloids

The self-assembly of short peptides into catalytic amyloid-like nanomaterials has proven to be a powerful tool in both understanding the evolution of early proteins and identifying new catalysts for practically useful chemical reactions. Here we demonstrate that both parallel and antiparallel arrangements of β-sheets can accommodate metal ions in catalytically productive coordination environments. Moreover, synergistic relationships, identified in catalytic amyloid mixtures, can be captured in macrocyclic and sheet-loop-sheet species, that offer faster rates of assembly and provide more complex asymmetric arrangements of functional groups, thus paving the way for future designs of amyloid-like catalytic proteins. Our findings show how initial catalytic activity in amyloid assemblies can be propagated and improved in more-complex molecules, providing another link in a complex evolutionary chain between short, potentially abiotically produced peptides and modern-day enzymes.     

Tuning fermi level and band gap in Li4Ti5O12 by doping and vacancy for ultrafast Li+ insertion/extraction

Li₄T_i5O₁₂ (LTO) attracts great interest due to the “zero strain” during cycles but the poor electronic and ionic conductivity critically impede the practical application. Herein, we report a synergy strategy of tuning localized electrons to shift Fermi level and band gap by Mg/Zr co-doping and oxygen vacancy incorporation, which significantly improves Li⁺ and electronic transport. More importantly, the intrinsic synergistic mechanism has been revealed by neutron diffraction, X-ray absorption spectra, and first-principles calculations. The “elastic effect” of lattice induced by Mg/Zr co-doping allows LTO to accommodate more oxygen vacancies to a certain degree without a severe lattice distortion, which largely improves the electronic conductivity. Mg/Zr co-doping and oxygen vacancy incorporation effectively enhanced the dynamic characteristics of LTO electrode, achieving the excellent rate performance (90 mAh/g at 20C) and cycle stability (96.9% after 500 cycles at 10C). First-principles calculations confirm Fermi level shifts to the conduction band, and the band gap becomes narrowed due to the synergistic modulation, and the intrinsic mechanism of the enhanced electronic and Li-ion conductivity is clarified. This study offers some insights into achieving the fast Li⁺ insertion/extraction by tuning the crystal and electronic structure with lattice doping and oxygen vacancy engineering.