Engineering Morphologies of Cobalt Pyrophosphates Nanostructures toward Greatly Enhanced Electrocatalytic Performance of Oxygen Evolution Reaction

Herein, a surfactant‐ and additive‐free strategy is developed for morphology‐controllable synthesis of cobalt pyrophosphate (CoPPi) nanostructures by tuning the concentration and ratio of the precursor solutions of Na₄P₂O₇ and Co(CH₃COO)₂. A series of CoPPi nanostructures including nanowires, nanobelts, nanoleaves, and nanorhombuses are prepared and exhibit very promising electrocatalytic properties toward the oxygen evolution reaction (OER). Acting as both reactant and pseudo‐surfactant, the existence of excess Na₄P₂O₇ is essential to synthesize CoPPi nanostructures for unique morphologies. Among all CoPPi nanostructures, the CoPPi nanowires catalyst renders the best catalytic performance for OER in alkaline media, achieving a low Tafel slope of 54.1 mV dec⁻¹, a small overpotential of 359 mV at 10 mA cm⁻², and superior stability. The electrocatalytic activities of CoPPi nanowires outperform the most reported non‐noble metal based catalysts, even better than the benchmark Ir/C (20%) catalyst. The reported synthesis of CoPPi gives guidance for morphology control of transition metal pyrophosphate based nanostructures for a high‐performance inexpensive material to replace the noble metal‐based OER catalysts.     

焦磷酸锰引发淀粉与丙烯腈接枝共聚及水解共聚物的性质

本文研究了焦磷酸锰引发淀粉与丙烯腈接枝共聚及淀粉—丙烯腈接枝共聚物(SPAN)水解制备高吸水性树脂(HSPAN),研究了影响 HSPAN 吸水率和吸液率的因素,结果表明:SPAN 的接枝效率>95%,接上百分数为55～65%:HSPAN吸去离子水522ml/g、自来水302ml/g,吸合成血88ml/g、合成尿86ml/g、0.9NaCl%溶液88ml/g.     

智能称重系统在三聚氰胺中的应用

通过对三聚氰胺称重系统偏差大、稳定性差、合格率低等原因进行分析,找到了问题的真正原因,并通过对其包装控制系统实施改造,从而使此问题得到彻底的解决。     

Preparation of Mesoporous Zirconium Phosphate-Pyrophosphate with a Large Amount of Thermally Stable Acid Groups on the Pore Surface

Mesoporous zirconium phosphate pyrophosphate of composition Zr(P₂O₇)_0.81(O₃POH)_0.38 was obtained by calcination at 600°C of a mesoporous zirconium phosphite diphosphonate, Zr[(O₃P-C₆H₄-PO₃)_0.54 (O₃P-C₆H₄-PO₃H₂)_0.13(O₃PH)_0.79]. The surface area of this completely inorganic material (215 m²/g) was lower than that of its inorgano-organic precursor (350 m²/g); however, both materials exhibited the same pore distribution, with an average pore diameter of 4 nm, and similar values of the mesopore volume (0.21 and 0.28 cm³/g, respectively). These results showed that the thermal treatment at 600°C leaves nearly unaltered the mesoporous structure of the precursor. ³¹P solid state NMR and TEM investigations were also carried out and discussed. The material obtained represents a considerable advancement in the preparation of zirconium phosphates with high surface area. Due to the good thermal stability of its surface acid groups (700–800°C), it is of interest for potential uses as an acid catalyst at high temperature.     

Formation and evolution of phosphorus-containing species during high-temperature oxidation of TiAl dipped in a low-concentrated phosphoric acid solution

TiAl samples were dipped in a low-concentrated phosphoric acid solution, air dried, then heated to 800 °C under argon gas before oxidation under reconstituted air at this temperature. At the end of the heating ramp, sample surfaces were covered by a titanium pyrophosphate (TiP₂O₇) layer, well adhered to the substrate. This pyrophosphate was shown to be detectable from 400 °C. Chemical reactions have been proposed for the formation of this compound. TiP₂O₇ coating strongly increased the oxidation resistance of TiAl at 800 °C for 100 h. After 100 h, a transition period occurred leading to the change of TiP₂O₇ into TiO₂, which was achieved after 230 h, total mass gain always remaining below that of raw substrate. This evolution was demonstrated not resulting from a thermal decomposition of pyrophosphate compound.     

Studies on the chemical, physical and mechanical properties of high-solids clearcoats prepared from hydroxyl-terminated isophthalate-based oligoesters and a melamine resin

A series of high-solids (solvent-free) clearcoats was prepared from hydroxyl-terminated isophthalate-based oligoesters and the hexakis(methoxymethylol)melamine resin (HMMM). The oligoesters, which were used as binders, were prepared via a transesterification reaction of dimethyl isophthalate (DI) under various molar ratios R (=mol ratio diols/diester) with a mixture of 1,6-hexanediol (HD) and 2-methyl-1,3-propanediol (MP). Mixtures of the two diols of different composition R_d (=mol ratio HD/MP), were used as well. An attempt was made to investigate and correlate the chemical, physical and mechanical properties of the formulated solvent-free clearcoats to: (a) the amount of the cross-linker (melamine resin); (b) the curing conditions (time and temperature); (c) the synthetic parameters applied in the preparation (via transesterification) of the oligoesters (e.g. excess of the diols in reaction with the DI and the molar ratio between the two diols, the species of the Lewis acid catalyst). The properties of all the new formulated high-solids clearcoats were compared to those of a reference clearcoat and their cross-linking was correlated to their chemical structure and composition as well as to their T_g values. It was found that the R and R_d values applied in the synthesis of the oligoesters (binders) significantly affected the performance of their corresponding clearcoats. More specifically, the clearcoats obtained from binders where 3<R<4, combined an enhanced processability, higher values of non-volatiles (80%) (lower VOC content) and better or comparable chemical, physical and mechanical properties (e.g. impact resistance, gasoline resistance, mar resistance, flexibility and pencil hardness) upon comparison to those of the reference clearcoat.     

Influence of the nanostructure and morphology of (VO)2P2O7 on its catalytic reactivity

The reoxidability of vanadyl pyrophosphate is studied by thermal analysis and by temporal analysis of product (TAP). The samples differ by surface area, oxidation state of vanadium, crystallite size, and degree of crystallinity. The morphology ranges from platy to prismatic and the microstructure from mosaic crystals exhibiting {100} faces to bulky crystals. The reactivity of these samples during oxidation as well as their catalytic reactivity studied in flow reactor is accounted for by the microstructure. The highest reoxidation capability and the best catalytic properties in oxidation of n-butane to maleic anhydride are obtained with mosaic crystals. This revised version was published online in July 2006 with corrections to the Cover Date.     

Activation of VOHPO4 · 0.5H2O in Propane/Air Mixture: Effect on Structural, Morphological, Oxidant’s Behaviour and Catalytic Property of (VO)2P2O7 Catalysts for Propane Oxidation

VOHPO₄ · 0.5H₂O synthesized by VOPO₄ · 2H₂O and isobutanol was activated in a flow of propane/air mixture (1% propane in air) at 673 K for 36, 75 and 132 h. Three vanadyl pyrophosphate catalysts obtained were denoted as VPD36P, VPD75P and VPD132P. The crystallinity of all propane/air pretreated catalysts as shown in XRD increased with the duration of calcination. SEM micrographs showed the formation of more isolated platelets and more prominent rosebud-shape agglomerate as the pre-treatment was longer. Four reduction peaks maxima at 752, 920, 1026 and 1140 were observed in the rate of hydrogen consumption for VPD36P. As the calcination duration increased to 75 h, the H₂ reduction peaks were shifted to lower temperatures at 750, 882, 1004 and 1140 K. When the calcination duration was further increased to 132 h, only three reduction peaks were observed at 752, 952 and 1142 K. Despite the progressively shifted of the major reduction peak maximum as the duration of calcination increased from 36 to 132 h, the lattice oxygen from VPD36P was found to be the most reactive. The catalytic performance for propane oxidation to acrylic acid (AA) showed that VPD36P gave the highest activity (9.6%) with 83.0% of selectivity to AA.     

The investigation on the flame retardancy mechanism of nitrogen flame retardant melamine cyanurate in polyamide 6

Melamine cyanurate (MCA) flame retardant polyamide 6 (PA6) shows good flame retardancy, but the corresponding mechanisms have not been completely understood. In this paper, Fourier transform infrared spectra (FTIR), elemental analysis (EA), scanning electronmicroscope (SEM), energy dispersive scanning (EDS), thermogravimeric analysis (TGA) and pyrolysis-gas chromatogram-mass spectrometer (Py-GC-MS) were conducted to investigate the processes including melt-drip phase, gaseous phase and condensed phase of MCA/PA6 system. Compared with original PA6, it is found that MCA flame retardant PA6 mainly undergoes predominant weak bond-breakage degradation forming oligomers rather than oxidative degradation producing low-boiling point fuel as original PA6 does. The produced oligomers can accelerate the formation of the melt drips which effectively removes the combustion heat and latent fuel, also the self-condensation of these oligomers is advantageous to form stable cross-linking structure, thus greatly consolidating the char layer.     

三聚氰胺产需现状与发展

对国内外三聚氰胺的生产与消费现状、发展历史、生产工艺、产需能力分布等进行了分析，并对国内外市场进行预测。