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Gang Pan

Publications and source records attributed to Gang Pan.

27 records · Page 2Linked to original sources

[Effect of growth phase on the flocculation of algal cells using clays].

Four different growth phases, late lag phase, middle logarithmic phase, late logarithmic phase and early senescence phase of Microcystis aeruginosa 469 were studied for their surface hydrophobicity (xylene-water system) and surface charge (Zeta potential), followed by flocculation tests with sepiolite of 0.2 g/L. The results showed that the values of hydrophobicity were 64%, 48%, 58% and 70%, and the algal removal efficiencies after 60 min were 97%, 87%, 81% and 99% respectively, indicating a good relationship between surface hydrophobicity and removal efficiency (R = 0.7-0.8), but not the surface charge. Surface hydrophobicity and removal efficiency for the algal cells of Microcystis aeruginosa both varied with growth phase in a sequence of senescence phase > lag phase > logarithmic phase.

Aluminum Silicates↗

Digital holography of particle fields: reconstruction by use of complex amplitude.

Digital holography appears to be a strong contender as the next-generation technology for holographic diagnostics of particle fields and holographic particle image velocimetry for flow field measurement. With the digital holographic approach, holograms are directly recorded by a digital camera and reconstructed numerically. This not only eliminates wet chemical processing and mechanical scanning, but also enables the use of complex amplitude information inaccessible by optical reconstruction, thereby allowing flexible reconstruction algorithms to achieve optimization of specific information. However, owing to the inherently low pixel resolution of solid-state imaging sensors, digital holography gives poor depth resolution for images, a problem that severely impairs the usefulness of digital holography especially in densely populated particle fields. This paper describes a technique that significantly improves particle axial-location accuracy by exploring the reconstructed complex amplitude information, compared with other numerical reconstruction schemes that merely mimic traditional optical reconstruction. This novel method allows accurate extraction of particle locations from forward-scattering particle holograms even at high particle loadings.

Journal Article↗

[Toxic effects of hexavalent chromium on the growth of blue-green microalgae].

A standard method of algal bioassay for determining the toxicity of toxic chemicals was applied to the interaction between Cr(VI) and six blue-green microalgae. The 96h-EC50 of hexavalent chromium on the growth of Chlorella pyrenoidosa, Synechococcus, Spirulina maxima, Spirulina platensis, Selenastrum capriornutum and Scenedesmus quadricauda were 4.96, 6.50, 11.16, 11.74, 12.43 and 20.89 mg/L, respectively. The tolerance of the six blue-green microalgae to Cr(VI) was in the order of Scenedesmus quadricauda > Selenastrum capriornutum > Spirulina platensis > Spirulina maxima > Synechococcus > Chlorella pyrenoidosa. The sensitivity of these species to Cr(VI) might relate to the cell size, the structure of cell wall, as well as the redox reaction caused by the exudate or enzyme. X-ray absorption near edge structure(XANES) was used to study the accumulation and transformation of Cr(VI) in Chlorella pyrenoidosa.

Carcinogens, Environmental↗

[EXAFS studies on adsorption-desorption mechanism of Zn at the manganite-water interface].

Microscopic structures of Zn(II) surface complexes adsorbed at the manganite(gamma-MnOOH)-water interface were studied using extended X-ray absorption fine structure(EXAFS) spectroscopy. Quantitative analysis of the EXAFS spectra showed that, in a 0.1 mol/L NaNO3 solution of pH 7.5, Zn(II) was adsorbed onto the solid surface by sharing the oxygen atom in the hydrous Zn2+ ions and in the structural unit MnO6 on the manganite surface. Most of the adsorbed Zn(II) was in the form of octahedral Zn(H2O2)(6)2+, but part of Zn(II) was adsorbed as tetrahedral Zn(OH)2 or Zn(OH)(4)2-. The average Zn-O bond length was 1.998 +/- 0.010 A (n = 3). The ZnO polyhedron of the hydrous Zn2+ ions was linked to the octahedron MnO6 of the manganite in two modes by sharing two O atoms on the edges of the polyhedral and/or one O atom on the corners of the polyhedral. EXAFS analysis of the second sphere indicated that Zn (II) adsorbed on the manganite resulted in two Zn-Mn atomic distances of 3.08 +/- 0.024A (n = 3) (R1) and 3.54 +/- 0.018 A (n = 3) (R2), corresponding to the edge-linkage (stronger adsorption site) and corner-linkage (weaker adsorption site), respectively. This result confirmed the basic hypothesis of Metastable Equilibrium Adsorption (MEA) theory from a molecular level that adsorption density gamma (mol/m2) is not a state variable, because adsorption density for the same adsorbate may have different chemical potential values due to different microscopic structure and adsorbate energy status. Macroscopic adsorption-desorption experiments showed that adsorption of Zn(II) onto manganite was largely irreversible (big adsorption hysteresis). EXAFS results indicated that the microscopic mechanism for the adsorption irreversibility was corresponded to the strong adsorption sites of edge sharing linkage between the adsorbate and adsorbent polyhedra.

Adsorption↗

[EXAFS studies on adsorption-desorption mechanism of Zn at delta-MnO2-water interface].

Microscopic structures of Zn(II) surface complexes adsorbed at a delta-MnO2-water interface were studied using extended X-ray absorption fine structure (EXAFS) spectroscopy. In a 0.1 mol/L NaNO3 solution of pH 5.50, Zn(II) was adsorbed onto the solid surface in the form of octahedral hydrous Zn(II) ions. The octahedral Zn(II) was linked to the structural unit of octahedral MnO6 of the delta-MnO2 surface by sharing the O atoms. The average bond length of RZn-O was (2.071 +/- 0.007)A (n = 3) and the Zn-Mn atomic distance was (3.528 +/- 0.006) A (n = 3), which corresponded to a corner-sharing linkage adsorption mode (weaker adsorption). Macroscopic adsorption-desorption isotherm experiments showed that, in contrast to that of Zn-manganite, adsorption of Zn(II) on delta-MnO2 was highly reversible and no apparent adsorption hysteresis was observed. EXAFS results indicated that the microscopic mechanism for the high adsorption reversibility was corresponded to the weak adsorption sites of corner sharing linkage between the adsorbate and adsorbent polyhedra.

Adsorption↗

[Kinetics and mechanism of removing Microcystis aeruginosa using clay flocculation].

Twenty-six natural clays were studied for their kinetics of flocculating and removing algal cells of Microcystis aeruginosa. According to the 8 h equilibrium removal efficiencies and removal rates at a clay-loading of 0.7 g.L-1, all the 26 clays were classified into three categories. Type-I clay, which includes talc, ferric oxide, sepiolite, ferroferric oxide, and kaolinite, has an equilibrium removal efficiency greater than 90%, a t50 (time needed to remove 50% of the algae) of less than 30 min, and a t80 (time needed to remove 80% of the algae) of less than 2.5 h. Type-II clay, which includes argillanceous rocks, attapulgite, rectorite, illite, and argil, etc., has an equilibrium removal efficiency of 50%-80%, a t50 of less than 2.5 h, and a t80 of more than 5 h. Type-III clay consists of 14 minerals, including laterite, zeolite, mica, clinoptilolite, pumice, tripoli, feldspar and quartz, etc. with the removal efficiency less than 50%, and t50 > > 8 h. When the clay loading was decreased to 0.1-0.2 g.L-1, the 8 h equilibrium removal efficiencies for 25 clays declined to below 60%, except for sepiolite, a Type-I clay, which maintained around 90%. After the sepiolite was modified with Fe3+ to increase its surface charge (Zeta potential from -24.0 mV to +0.43 mV at pH 7.4), the initial removal rate was increased remarkably although its 8 h equilibrium removal efficiency was not improved substantially. As a comparison, the 8 h equilibrium removal efficiency of PAC was no greater than 40% at loadings of 0.02-0.2 g.L-1. Following the analysis of the flocculation mechanism it was concluded that the effect of bridging and netting may play a key role in the clay-algae flocculation processes, which may be important for selecting and modifying clays to improve significantly the removal efficiency.

Aluminum Silicates↗

Adsorption-desorption of phosphate on airborne dust and riverborne particulates in East Mediterranean seawater.

The potential importance of adsorption-desorption behavior of phosphorus (P) on the East Mediterranean (E. Med) P cycle was investigated. Contrasting adsorption behavior between Saharan dust (SD) and Nile particulate matter (Nile PM) was observed. SD was a source of P to the region, which released an average of 3.3 +/- 0.3 micromolP/g into the surface seawater and showed no adsorption ability under the conditions close to the E. Med deep water. Saharan dust is therefore unlikely to be the reason for P limitation in the region. By contrast, Nile PM acted dual roles of a sink and source of P in different waters (surface seawater, deep seawater, and river water). A new crossover-type adsorption-desorption model explained the contrasting adsorption behavior and the dual nature of natural particles. The model indicates that when natural particles are transported between different waters, they can be a sink (adsorption) or a source (desorption) of phosphorus depending on the "specific concentration (lambda)", which is the ratio between the aqueous P concentration and the zero equilibrium P concentration (EPC0). EPC0 refers to the solute concentration value where the adsorption isotherm crosses over the aqueous concentration axis. When lambda > 1, adsorption occurs, whereas when lambda < 1, desorption occurs. The model added a general development to the methodology of adsorption isotherm, where, for the first time, effects of solute concentration, solid concentration, and aqueous medium (EPC0) on the adsorption and desorption of P in natural waters were simultaneously described by a single equation. Using the model, it was quantitatively reconstructed that particles emitted during the pre-1964 Nile floods could be a major source of P to Egyptian coastal waters (up to 4800 tonsP/yr), greater than the dissolved P flux (approximately 3200 tonsP/yr), but a trapper of dissolved phosphate in E. Med deep waters.

Adsorption↗

Toxicity and bioaccumulation of copper in three green microalgal species.

The effective concentrations of copper on the inhibition of the growth of Scenedesmus obliquus, Chlorella pyrenoidosa and Closterium lunula at 96 h (96 h EC50) were determined to be 50, 68 and 200 microg/l, respectively. The low initial bioaccumulation of Cu by C. lunula was found to be responsible for its tolerance to Cu. The amount of Cu accumulated by all three microalgae reached the maximum value and decreased quickly after the peak followed by a slow decrease over the next 6 d. Bioaccumulation of Cu by C. lunula was directly proportional to the initial Cu concentration. After reaching the first peak after 1 d, the bioconcentration factor of Cu by microalgae declined to its minimum value during the exponential growth phase but increased in the stationary growth phase again. This indicates that desorption of Cu from microalgae was higher during the exponential growth phase but lower in the stationary growth phase. Smaller microalgae with low 96 h EC50 values are more efficient in removing Cu from wastewater.

Chlorella↗

Effect and mechanism of inorganic carbon on the biodegradation of dimethyl phthalate by Chlorella pyrenoidosa.

The effect and mechanism of inorganic carbon (IC) on the biodegradation of dimethyl phthalate (DMP) by a green microalga Chlorella pyrenoidosa was investigated. It was indicated that DMP could be used as the sole carbon source to support the slow heterotrophic growth of C. pyrenoidosa, but both the growth of C. pyrenoidosa and the biodegradation rate of DMP were obviously increased when initial inorganic carbon concentration (IC) was increased from 0.6 to 23.7 mg/l. Phthalic acid (PA) was found to be an intermediate product of DMP biodegradation and accumulated in the culture solution, which caused a sharp decrease in pH of medium and inhibited both the growth of alga and the biodegradation of DMP. The role of IC for improving the biodegradation of DMP was both to supply a favorite carbon source to support the rapid growth of alga and to mitigate the decrease of pH because of the production of PA. A suggested second-order kinetic equation of organic pollutant biodegradation by microalgae (-dC/dt = KNr) fitted well with the experimental data and the correlation coefficients were all above 0.9. The second-order constant (K) apparently declined with the increase of initial IC because lower ratio between organic carbon from DMP and IC was used to support the growth of alga when initial IC increased.

Biodegradation, Environmental↗