Modeling and mechanism of the adsorption of copper ion onto natural bamboo sawdust.

The sorption of copper ions onto natural bamboo sawdust with cellulose-lignin polymeric structure strongly depends on pH. The adsorption capacity for copper ions increases as increasing pH and copper loadings. The fitting of copper pH boundary curve by NEM surface complexation models shows that: three-sites model including the ion exchange reaction of permanent charge fits better than two-sites model. The incorporation of the hydrated ion reaction gives better fitting results. XAFS study shows that: copper ions mainly form inner complexation with sawdust, but there is no obvious evidence on the complexation of carboxylic acid groups with copper ions. EXAFS fitting result shows that: as pH rises, the spatial configuration of copper ions shifts from tetrahedron to octahedron. Meanwhile the increase in the coordination number indicates that hydrated copper ions participate in the adsorption. Both XANES and EXFAS spectrum offer a similar explanation for copper adsorption in the range of experimental and fitting errors.

Optimization of ethylenediamine-grafted multiwalled carbon nanotubes for solid-phase extraction of lead cations.

INTRODUCTION: Ethylenediamine-grafted multiwalled carbon nanotubes (MWCNTs-EDA-I and MWCNTs-EDA-II) are optimized and employed to investigate the preconcentration of lead ions (Pb(II)) in trace level. RESULTS: The results show that Pb(II) can be adsorbed quantitatively on the optimized MWCNTs in the range of pH 4-7 and MWCNTs-EDA-I has a higher maximum Pb(II) adsorption capacity (157.19 mg/g) than MWCNTs-EDA-II (89.16 mg/g). The adsorbed Pb(II) can be eluted completely using 5 mL of 1 mol/L HNO(3). DISCUSSION: A new approach using a microcolumn packed with the obtained MWCNTs-EDA-I has been developed for the preconcentration of trace amount of Pb(II). Parameters influencing the preconcentration of Pb(II), such as pH of the sample, sample volume, elution solution, and interfering ions, have been examined and optimized in detail. Under optimum experimental conditions, the limit of detection is 0.30 ng/mL with the enrichment factor of 60. The relative standard deviation (R.S.D) was 2.6% at the 20 ng/mL Pb(II) level. CONCLUSION: The method has been applied for the preconcentration of trace amount of Pb(II) in environmental water samples with satisfying results.

Efficient two-photon-sensitized luminescence of a novel europium(III) ß-diketonate complex and application in biological imaging.

A novel europium(III) ß-diketonate complex exhibiting bright two-photon-sensitized luminescence is synthesized and applied as a two-photon-sensitized luminescent probe to stain DNA in live cells.

Formation of shaped barium sulfate-dye hybrids: waste dye utilization for eco-friendly treatment of wastewater.

PURPOSE: Owing to the present complexity and difficulty of concentrated dye wastewater treatment, this work aimed to synthesize a reproducible waste-sorbing material for the treatment of wastewater by forming the dye-conjugating complex hybrid. METHODS: The inorganic/organic hybridization was applied to prepare the objective material by immobilizing waster dye-Mordant blue 9 (MB) with barium sulfate (BaSO4). The composition and pattern of the formed material were determined by spectrometry and characterized by SEM and XRD, and their formation process was clarified. The adsorption of cationic dye-basic blue BO (BB) and copper ion was investigated. RESULTS: The hybrid of MB alone into growing BaSO4 formed the pineapple-like particles while that of the MB/BB-conjugating complex was the rhombus material. The adsorption of BB on the MB-BaSO4 hybrid was probably attributed to ion-pair equilibrium and that of Cu2+ may result from the complexation. The treatment of dye and heavy metal wastewaters indicated that the MB hybrid material removed 99.8% BB and 97% Cu2+ and the dye-conjugating hybrid with growing BaSO4 100% MB, 99.5% BB, and 44% Cu2+. CONCLUSION: The waste MB-BaSO4 hybrid material is efficient to treat cationic dye and Cu2+ wastewater. The dye-conjugating hybridization method is the first to be advanced for in situ wastewater treatment, and it showed a combined effect for the removal of both organic dyes and heavy metals.

Preparation of dye waste-barium sulfate hybrid adsorbent and application in organic wastewater treatment.

A new hybrid material was developed by the template-free hybridization of weak acidic pink red B (APRB, C.I. 18073) with BaSO(4). The composition and structure of the material were determined and characterized. In contrast to conventional sorbents, the hybrid material has a specific surface area of 0.89 m(2)/g, but it contains lots of negative charges and lipophilic groups as the basis of specific adsorption. The efficient removal of cationic dyes and persistent organic pollutants (POPs) indicates that it has an improved adsorption capacity and selectivity with a short removal time less than 2 min; while the hybrid sorbents fit the Langmuir isotherm model, and follow the octanol-water partition law. Instead of using APRB reagent, an APRB-producing wastewater was reused to prepare the cost-effective sorbent, and the equilibrium adsorption capacities of which reached 222 and 160 mg/g for EV and BPR, respectively. The sorbents was then used to treat three wastewater samples with satisfactory results of over 97% decolonization and 88% COD-decreasing. In addition, the hybrid sorbent was regenerated from sludge over five cycles, and its adsorption capacity was not appreciably changed. This work has developed a simple and eco-friendly method for synthesizing a practical and efficient sorbent.

Sensitive determination of anionic surfactants in water with trans-4-[4'-(N-methyl-N-hydroxylethylamino)-cinnamyl-N-9-(4'-(2,2':6',2''-terpyridine))-phenylmethylene]pyridine bromide by the light-absorption ratio variation approach.

The light-absorption ratio variation approach was described and applied to the determination of anionic surfactants (AS) in water with a novel chromophore, trans 4-[4'-(N-methyl-N-hydroxylethylamino)-cinnamyl-N-9-(4'-(2,2':6',2''-terpyridine))-phenylmethylene]pyridine bromide (BTMHCTPP). The complexations between BTMHCTPP and sodium dodecyl sulfate (SDS) and sodium dodecylbenzenesulfonate (SDBS) at pH 3.85 were characterized by the break point approach. Results have shown that both 1BTMHCTPP:1SDS and 1BTMHCTPP:1SDBS complexes were formed, and that deltaA(r) (deltaA(r) = light-absorption ratio variation) is linear for the range of AS between 0.05 and 1.00 mg/L. The limits of detection (3sigma) are 0.045 mg/L for SDS and 0.040 mg/L for SDBS. The complexation is selective in the presence of EDTA, and it has been applied to the analysis of water samples with satisfactory results.

Tetraiodophenolsulfonphthalein as a spectral substitute to characterize the complexation between cationic and anionic surfactant.

The complexation of cetyltrimethylammonium bromide (CTAB) with sodium dodecyl sulfate (SDS) with sodium dodecyl benzene sulfonate (SDBS), with tetraiodophenolsulfonphthalein (TIPST) as a spectral substitute was investigated at pH 5.89 and 8.30 by the microsurface adsorption--spectral correction (MSASC) technique. The aggregations of TIPST, SDS, and SDBS on CTAB obeyed the Langmuir isothermal adsorption. The aggregates TIPST-CTAB, TIPST2-CTAB3, SDS3-CTAB2, and SDBS3-CTAB2 were formed at 20 degrees C and the binding constants of all the aggregates were determined. The replacement of TIPST-binding CTAB monomer with SDS or SDBS at pH 5.89 was applied to the quantitative determination of anionic detergent (AD) in water with satisfactory recovery.