Removal of phosphate by layered double hydroxides containing iron

Iron-based layered double hydroxides (M2+(a)Fe3+(b) (OH)2(a+b) CO3(2-) b/2mH2O) were synthesized. Removal of phosphate by the compounds was studied from the viewpoint of buffering pH effect of the compounds and buffering capacity of solution. The compounds released metal cations (Mg2+, Ca2 , Fe3+) and/or their hydroxides responding to various water environments due to their buffering pH function. The released cations and/or hydroxides worked effectively as coagulants for the phosphate removal. The removal of phosphate depended on the buffering capacity of the solution that is the function of the solution pH and the concentration of phosphate. The removal of phosphate from the solution with small buffering capacity followed a Langmuir-type isotherm. The removal of phosphate from the solution with larger buffering capacity was largely increased. The removal of phosphate by the compounds was analyzed based on the model describing the buffering pH effect of the compounds from which the amount of released cations (CB) can be determined. The removal was well correlated with the amount of dissolution of the compounds, CB. The mechanism of phosphate removal was examined based on the removal efficiency (mol of removed phosphate/mol of released alkali). The efficiencies showed below one in the solution with large buffering capacity and above one in the solution with small buffering capacity. The efficiency below one showed the removal of phosphate through coagulation by the released metal cations and hydroxides. The successful removal of dilute phosphate (0.2mg P/l) from the drain water was also demonstrated.     

Electro-conductive porous ceramics prepared by chemical vapor infiltration of TiN

Using pressure-pulsed chemical vapor infiltration (PCVI) method, TiN was partially infiltrated at 850 °C from gas system of TiCl₄ (1%)–N₂ (10%)–H₂ into the highly porous carbon substrates prepared by the carbonization of cotton-wool, filter paper, and wood at 1,000 °C in Ar for 4 h. After 10,000 pulses of PCVI, electro-conductive porous ceramics having the three-dimensionally continuous current paths were obtained, which had the porosity of 80% and more, the resistivity of 10⁻⁵–10⁻⁶ Ω m, and the average pore sizes of 10–40 μm. The geometric surface area per unit volume of the sample was higher than that of the conventional foil-type current collector for lithium-ion battery. The surface area showed the highest value for the sample obtained from carbonized wood substrate.     

Structural and Physicochemical Properties of Endosperm Starches Possessing Different Alleles at the Amylose-extender and Waxy Locus in Maize (Zea mays L.)

The structure and some physicochemical properties of endosperm starches from seven amylose-extender (ae) and two waxy (wx) alleles of maize (Zea mays L.) were studied. Starches prepared from mature kernels of six ae mutants, Oh43 inbred line ae (standard ae), ae-RWB-2 and ae-RWB-3, and W23 × L317 hybrid line ae-PP, ae-Bol 561 and ae-emll, were uniquely ae type, as was concluded from B type X-ray diffractograms; high gelatinization temperatures determined by differential scanning calorimetry (DSC); with poor starch-granule digestibility to amylase; high amylose (37—45 %) and high intermediate fraction (13—18 %) contents; and low ratios (1.0—1.2) of long α-1,4-chains to short α-1,4-chains of amylopectin determined by gel permeation chromatography (GPC) of isoamylase-debranched starches. The results also indicated that different ae alleles had different effects on the amylose content of endosperm starches. Mature kernels of Oh43 ae-RWB-1 mutant showed tarnished and translucent phenotype characteristics of the ae genotype but contained endosperm starch with 21—22 % of amylose which was lower than that of the Oh43 normal counterpart. Both wx-B and wx-C (standard wx) genes have similar effect on structure and physicochemical properties of waxy starches of A632, B37, C105, Oh43, and W64A inbred lines.