A novel polyamine microsphere, prepared from the water-in-oil emulsion of polyethylenimine, was characterized. The investigation of scanning electron microscopy showed that the polyamine microsphere is a regular ball with a smooth surface. The diameter distribution of the microsphere is 0.37–4.29 μm. The isoelectric point of the microsphere is 10.6. The microsphere can adsorb proteins through the co-effect of electrostatic and hydrophobic interactions. Among the proteins tested, the highest value of adsorption of microsphere, 127.8 mg·g−1 microsphere, was obtained with lipase. In comparison with other proteins, the hydrophobic force is more important in promoting the adsorption of lipase. The microsphere can preferentially adsorb lipase from an even mixture of proteins. The optimum temperature and pH for the selective adsorption of lipase by the microsphere was 35 °C and pH 7.0.
In this article, theoretical analysis and different testing techniques were used to study the reaction pathways and synthesized products of phosphoric acid and aluminum hydroxide at different Al/P molar ratios. The results show that: (a) When the molar ratio of phosphoric acid/aluminum hydroxide is 1:3, the reaction will produce stoichiometric aluminum dihydrogen phosphate (Al(H 2 PO 4 ) 3 ); (b) when Al(OH) 3 is excessive, an intermediate, monohydroxy aluminum dihydrogen phospate (HO-Al-(H 2 PO 4 ) 2 ), will appear, which is unstable and will continue to react according to two reaction pathways, one is intramolecular dehydration to form phosphoric acid hydrogen-dihydrogen aluminum diphosphate (H 2 PO 4 )Al(HPO 4 ); the other is intermolecular dehydration cross-linking to form a polymeric macromolecular aluminum phosphate H-((HPO 4 )(H 2 PO 4 )Al-O-HPO 4 -Al(H 2 PO 4 )-O)n H. The ratio of the two pathways is affected by the excess of Al(OH) 3 . When the excess of Al(OH) 3 continues to increase, the ratio of the second reaction path begins to increase and the viscosity of the product gradually increases. Adhesion experiments show that the aluminum dihydrogen phosphate has the best bonding performance benefiting from its lower viscosity.
K E Y W O R D SAl/P molar ratio, aluminum phosphate binder, bonding performance, composition, reaction route
It is important to develop new energy storage and conversion technology to mitigate the energy crisis for the sustainable development of human society. In this study, free-standing porous nitrogen-doped carbon fiber (PN-CF) membranes were obtained from the pyrolysis of Zn–MOF-74/polyacrylonitrile (PAN) composite fibers, which were fabricated in situ by an electrospinning technology. The resulting free-standing fibers can be cut into membrane disks and directly used as an anode electrode without the addition of any binder or additive. The PN-CFs showed great reversible capacities of 210 mAh g−1 at a current density of 0.05 A g−1 and excellent cyclic stability of 170.5 mAh g−1 at a current density of 0.2 A g−1 after 600 cycles in sodium ion batteries (SIBs). The improved electrochemical performance of PN-CFs can be attributed to the rich porous structure derived by the incorporation of Zn–MOF-74 and nitrogen doping to promote sodium ion transportation.
Self‐doped TiO2 nanotube array (DTNA) electrodes were fabricated through anodic oxidation combined with cathodic reduction. The morphology and structural features of pristine TiO2 nanotube arrays and DTNA electrodes were studied through scanning electron microscopy, X‐ray diffractometry, and X‐ray photoelectron spectroscopy. An accelerated life test was used to test the electrode service lifetime and thus the electrode's stability. The service lifetime of the DTNA electrode prepared at constant 40 V for 6 hr was approximately 338.7 hr at constant 1 mA/cm2 in a 1 M NaClO4 solution. Methyl orange (MO) was employed as the degradation probe for measuring electrochemical oxidation performance. The color removal rate of 200 mg/L MO of the DTNA electrode (85.2% at 1 mA/cm2) was greater than that of the Ti/IrO2 electrode (31.1% at 1 mA/cm2). The larger the surface area of the DTNA electrode is, the more conductive the electrode is for the degradation of organic substances. Organic degradation on the DTNA electrode occurred primarily through an indirect pathway (producing [∙OH]).
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