Characterization of refractory matters in dyeing wastewater during a full-scale Fenton process following pure-oxygen activated sludge treatment.

Refractory pollutants in raw and treated dyeing wastewaters were characterized using fractional molecular weight cut-off, Ultraviolet-vis spectrophotometry, and high-performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI/MS). Significant organics and color compounds remained after biological (pure-oxygen activated sludge) and chemical (Fenton) treatments at a dyeing wastewater treatment plant (flow rate ∼100,000m(3)/d). HPLC-ESI/MS analysis revealed that some organic compounds disappeared after the biological treatment but reappeared after the chemical oxidation process, and some of that were originally absent in the raw dyeing wastewater was formed after the biological or chemical treatment. It appeared that the Fenton process merely impaired the color-imparting bonds in the dye materials instead of completely degrading them. Nevertheless, this process did significantly reduce the soluble chemical oxygen demand (SCOD, 66%) and color (73%) remaining after initial biological treatment which reduced SCOD by 53% and color by 13% in raw wastewater. Biological treatment decreased the degradable compounds substantially, in such a way that the following Fenton process could effectively remove recalcitrant compounds, making the overall hybrid system more economical. In addition, ferric ion inherent to the Fenton reaction effectively coagulated particulate matters not removed via biological and chemical oxidation.

Face-driven corner-linked octahedral nanocages: M6L8 cages formed by C3-symmetric triangular facial ligands linked via C4-symmetric square tetratopic Pd(II) ions at truncated octahedron corners.

The face-driven corner-linked truncated octahedral nanocages, [Pd6L8]12+ (1, L1 = N,N',N' '-tris(3-pyridinyl)-1,3,5-benzenetricarboxamide; 2, L2 = N,N',N' '-tris(4-pyridinylmethyl)-1,3,5-benzenetricarboxamide), were prepared with eight C3-symmetric tridentate ligands and six square planar tetratopic palladium(II) ions. The combination of the nitrogen donor atom at a approximately 120 degrees kink position of the carboxamido pyridinyl group and the tilted pyridyl versus the facial plane of the ligands can provide the needed curvature for the formation of octahedral cages. The nitrogen atoms can coordinate to the square planar palladium(II) ions to form kinks with approximately 120 degrees angles at the C4-symmetric square planar corners of the truncated octahedron. Depending on the conformation of the ligand, L1, two different truncated octahedral cages of around 2.4 nm in diameters were formed. The major form of 1 with syn-conformational ligands has a cavity volume of approximately 1600 A3. The cage has 12 ports (3.4 x 3.5 A2) at all edges of the octahedron. The minor form of cage 1 with anti-conformational ligands has a slightly increased cavity volume ( approximately 1900 A3) and port size (3.3 x 8.0 A2). The insertion of a methylene group in L2 has not only increased the cavity volume of 2 to approximately 2200 A3 but also enlarged the port size to 4.1 x 8.0 A2. However, an atomic force microscopy (AFM) study of cage 2 showed that the cages had a height of 1.8 +/- 0.1 nm. This value is about 30% smaller than the calculated size of 2.6 nm from the crystal structure. This tip-induced decrease in height in cage 2 suggests the nonrigidity of cage 2.