Biomedical subjects

X Z Li

Publications and source records attributed to X Z Li.

At least 19 recordsLinked to original sources

PubMed2005

Synthesis and ab initio X-ray powder diffraction structure of the new alkali and alkali earth metal borate NaCa(BO3).

A sodium calcium borate, NaCaBO3, has been synthesized by the solid-state reaction method and the structure solved from X-ray powder diffraction data. The compound crystallizes in space group Pmmn and has a desired structure type containing isolated planar BO3(3-) anions. Mixed occupancy is found to exist in the Ca site, with partial replacement by Na. One Ca/Na mixed atom and one Na atom are at sites with mm2 symmetry, and a second Ca/Na mixed atom, an Na atom, two B and two O atoms are on mirror planes.

Journal Article↗

PubMed2005

Computer programs for unit-cell determination in electron diffraction experiments.

A set of computer programs for unit-cell determination from an electron diffraction tilt series and pattern indexing has been developed on the basis of several well-established algorithms. In this approach, a reduced direct primitive cell is first determined from experimental data, in the means time, the measurement errors of the tilt angles are checked and minimized. The derived primitive cell is then checked for possible higher lattice symmetry and transformed into a proper conventional cell. Finally a least-squares refinement procedure is adopted to generate optimum lattice parameters on the basis of the lengths of basic reflections in each diffraction pattern and the indices of these reflections. Examples are given to show the usage of the programs.

Journal Article↗

PubMed2004

Syntheses, thermal stability, and structure determination of the novel isostructural RBa3B9O18 (R = Y, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb).

A novel borate compound YBa(3)B(9)O(18) has crystallized in a melt of BaYB(9)O(16). Single-crystal X-ray diffraction measurements reveal that YBa(3)B(9)O(18) adopts a hexagonal space group P6(3)/m with cell parameters of a = 7.1761(6) A and c = 16.9657(6) A. The structure is made up of the planar B(3)O(6) groups parallel to each other along the (001) direction, regular YO(6) octahedra, and irregular BaO(6) and BaO(9) polyhedra to form an analogue structure of beta-BaB(2)O(4). A series of isostructural borate compounds RBa(3)B(9)O(18) (R = Y, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb) were prepared by powder solid-state reactions. The DTA and TGA curves of YBaB(9)O(16) show an obvious weight loss at about 955 degrees C associated with a decomposition into YBO(3), B(2)O(3), and YBa(3)B(9)O(18) due to its incongruent melting behavior. The DTA and TGA curves of YBa(3)B(9)O(18) show that it is chemically stable and a congruent melting compound. A comparison of the structures of YBa(3)B(9)O(18) and beta-BaB(2)O(4) is presented.

Journal Article↗

PubMed2004

Enhanced photocatalytic degradation of VOCs using Ln3+-TiO2 catalysts for indoor air purification.

Two types of lanthanide ion-doped titanium dioxide (Ln3+-TiO2) catalysts including La3+-TiO2 and Nd3+-TiO2 were prepared by a sol-gel method. The effects of the lanthanide ion doping on the crystal structure, surface area, adsorption properties, pore size distribution, and surface chemical state of the catalysts were investigated by means of XRD, BET, and XPS. As results, the crystal size decreased significantly, while the specific surface area, t-plot total surface area, micropore volume, and the total pore volume increased owing to the lanthanide ion doping. The nitrogen adsorption-desorption isotherms of the catalysts showed that the N2 adsorption ability of the Ln3+-TiO2 catalysts was better than the TiO2 catalyst. Among them, the 0.7% Ln3+-TiO2 catalysts demonstrated the highest adsorption ability. The photocatalytic activity of the catalysts was investigated in the experiments of the photocatalytic degradation of benzene, toluene, ethylbenzene and o-xylene (BTEX) in a gaseous phase. The photocatalytic efficiency of the TiO2 catalysts with the lanthanide ion doping was remarkably enhanced by BTEX removal. The 1.2% Ln3+-TiO2 catalysts achieved the highest photocatalytic activity. The enhanced photodegradation of BTEX is possibly due to the improved adsorption ability and the enhanced electron-hole pairs separation due to the presence of Ti3+ on the surface of Ln3+-TiO2 catalysts and the electron transfer between the conduction band/defect level and lanthanide crystal field state.

Adsorption↗

PubMed2004

JECP/PCED--a computer program for simulation of polycrystalline electron diffraction pattern and phase identification.

A computer program for simulation of polycrystalline electron diffraction pattern and phase identification is described. In addition to simulating electron diffraction pattern for a single phase, the program has the ability to model two phases with selected mass ratio. Experimental polycrystalline electron diffraction patterns can be directly compared to simulated patterns for phase identification. Examples of how to use the program are also given.

Journal Article↗

PubMed2003

Three-dimensional reconstruction of the nu-AlCrFe phase by electron crystallography.

The three-dimensional (3D) structure of the huge quasicrystal approximant nu-AlFeCr (space group P6(3)/m, a = 40.687 and c = 12.546 A) was solved by electron crystallography. High-resolution transmission-electron-microscopy (HREM) images and selected-area electron diffraction patterns from 13 different zone axes were combined to give a 3D potential map. 124 out of 129 unique atoms were found in the 3D map. Procedures for ab initio structure determination by 3D reconstruction are given. It is demonstrated that 3D reconstruction from HREM images is very powerful for solving structures--even very complicated ones. There is no limit in terms of the number of unique atoms in a structure that can be solved by 3D reconstruction.

Journal Article↗

PubMed2003

Photocatalytic oxidation using a new catalyst--TiO2 microsphere--for water and wastewater treatment.

Since the suspended TiO2 powder enjoys free contact with UV irradiation in a photoreactor system, it can generally achieve better efficiency than the immobilized TiO2 catalysts. However, the separation and reuse of this catalyst powder from treated water often limit its application in practice. In this study, a new type of TiO2 catalyst called TiO2 microsphere was prepared by a sol-spraying-calcination method, which can easily settle in its aqueous suspensions under gravity. The SEM image of the TiO2 microsphere samples demonstrated that they had an almost spherical shape with a particle size of 30-160 microm, while the XRD analysis indicated that these TiO2 microspheres still had a crystal size of 8.1 nm. Since these TiO2 microspheres had a porous structure with higher specific surface area and pore volume than normal TiO2 powders, they appeared to have strong adsorption ability in its aqueous suspensions. The photocatalytic activity of the TiO2 microspheres was evaluated in the photodegradations of salicylic acid (SA) and sulfosalicylic acid (SSA). The experimental results showed that the reaction rate using the TiO2 microspheres was similar to that using the TiO2 powders in the SA suspensions and even higher than that in the SSA suspensions. Chemical and physical properties of the TiO2 microspheres and powders that are attributed to photoactivity were discussed based on the Langmuir-Hinshelwood kinetic model. The prepared TiO2 microsphere samples were reused in the photooxidation reaction more than 50 times. It was found that there was no significant weakening in their photoactivity and no change in their particle shape. This TiO2 microsphere catalyst can be simply used to conduct an effective photooxidation in its suspension for water and wastewater treatment with ease of recovery from treated water.

Catalysis↗

PubMed2003

The enhancement of TiO2 photocatalytic activity by hydrogen thermal treatment.

In this study, conventional TiO2 powder was heated in hydrogen (H2) gas at a high temperature as pretreatment. The photoactivity of the treated TiO2 samples was evaluated in the photodegradation of sulfosalicylic acid (SSA) in aqueous suspension. The experimental results demonstrated that the photodegradation rates of SSA were significantly enhanced by using the H2-treated TiO2 catalysts and an optimum temperature for the H2 treatment was found to be of 500-600 degrees C. The in situ electron paramagnetic resonance (EPR) signal intensity of oxygen vacancies (OV) and trivalent titanium (Ti3+) associated with the photocatalytic activity was studied. The results proved the presence of OV and Ti3+ in the lattice of the H2-treated TiO2 and indicated that both were contributed to the enhancement of photocatalytic activity. Moreover, the experimental results presented that the EPR signal intensity of OV and Ti3+ in the H2-treated TiO2 samples after 10 months storage was still significant higher than that in the untreated TiO2 catalyst. The experiment also demonstrated that the significant enhancement occurred in the photodegradation of phenol using the H2-treated TiO2.

Benzenesulfonates↗

PubMed2002

Photoelectrocatalytic degradation of humic acid in aqueous solution using a Ti/TiO2 mesh photoelectrode.

Humic acid (HA) is one of natural organics existing in water supply as a precursor of trihalomethanes formation in chlorination. The photo-degradation of HA in aqueous solution by photoelectrocatalytic (PEC) oxidation using a Ti/TiO2 mesh electrode was investigated in terms of UV absorbance at 254 nm, colour and TOC concentration. The key factors affecting the PEC oxidation efficiency were studied, including the concentration of electrolyte, electrical bias applied. pH value of HA solution, the intensity of incident light and the area of Ti/TiO2 mesh photoelectrodes. The first-order kinetic model was applied to describe the PEC oxidation, in which the kinetic constant k was verified by the experimental data as a function of the concentration of electrolyte, light intensity, the area of Ti/TiO2 mesh electrode and the voltage of electrical bias applied. It was found that there was an optimal bias voltage of 1.63 V and low pH value was favourable for TOC removal in HA solution. Our investigation showed that PEC oxidation was a convenient way to mineralise the organic matters with high efficiency.

Coloring Agents↗

PubMed2002

Enhancement of photocatalytic oxidation of humic acid in TiO2 suspensions by increasing cation strength.

This study aimed at improving the photocatalytic (PC) oxidation of humic acids (HA) in TiO2 suspensions by adding cationic ion such as calcium or magnesium. A set of tests was first conducted in the dark to study the adsorption of HA onto TiO2 in suspensions at different pH and calcium concentrations. The experiment demonstrated that the adsorption of HA onto the TiO2 particles was either pH-dependent or calcium strength-dependent due to electrostatic interaction and calcium ion bridging. The photodegradation of HA in the presence of UV irradiation was investigated as a function of pH and the concentration of calcium and magnesium ions. The results showed that the adsorption behavior between HA and TiO2 played a very important role during the PC oxidation process. The PC oxidation could be enhanced at neutral pH by increasing the cation strength. The kinetics of HA PC degradation in TiO2 suspensions with different initial concentrations was also studied using the Langmuir-Hinshelwood model.

Catalysis↗

PubMed2002

The enhancement of photodegradation efficiency using Pt-TiO2 catalyst.

This study investigates the mechanism of photosensitization and the recombination of excited electron-hole pairs affected by depositing platinum (Pt) on the surface of titanium dioxide (TiO2). A new catalyst of Pt-TiO2 was prepared by a photoreduction process. Being model reactions, the photocatalytic oxidation of methylene blue (MB) and methyl orange (MO) in aqueous solutions using the Pt-TiO2 catalyst was carried out under either UV or visible light irradiation. The experimental results indicate that an optimal content of 0.75%Pt-TiO2 achieves the best photocatalytic performance of MB and MO degradation and that the Pt-TiO2 catalyst can be sensitized by visible light. The interaction of Pt and TiO2 was investigated by means of UV-Vis absorption spectra, photoluminescence emission spectra, and X-ray photoelectron emission spectroscopy. The Pt0, Pt2+ and Pt4+ species existing on the surface of Pt-TiO2, and the Ti3+ species existing in its lattice may form a defect energy level. The Pt impurities, including Pt, Pt(OH)2, and PtO2, and the defect energy level absorb visible light more efficiently in comparison with the pure TiO2 and hinder the recombination rate of excited electron-hole pairs.

Catalysis↗

PubMed2002

MAP precipitation from landfill leachate and seawater bittern waste.

The leachates generated at Hong Kong landfill sites contain high strength of ammonium-nitrogen (NH4+-N) over 3,000 mg l(-1) and are generally inhibitive to most biological treatment processes. To remove the NH4+-N from the landfill leachates and also recover the nitrogen as a struvite fertilizer, a lab-scale study was performed to investigate the feasibility of NH4+-N removal and struvite crystallization using different magnesium sources. Three combinations of chemicals, MgCl2 x 6H2O+Na2HPO4 x 12H2O, MgO+H3PO4 and MgSO4 x 7H2O+Ca(H2PO4) x H2O, were first used at different molar ratios to precipitate NH4+-N from the leachate. The experimental results indicated that NH4+-N was removed by 92%, 36% and 70% respectively at pH 9.0 and a molar ratio of Mg:N:P=1:1:1. Two synthetic seawater bitten wastes containing Mg2+ at 9,220 mg l(-1) and 24,900 mg l(-1) respectively were then used as a magnesium source, while 85% H3PO4 chemical was used as a phosphorus source. The results revealed that NH4+-N was removed by 80% and 72% respectively, while a molar ratio of Mg:N:P=1:1:1 was applied. In the final stage of experiments, the magnesium-ammonium-phosphate (MAP) precipitates were examined by SEM, EDS and XRD. The SEM micrographs of the MAP precipitates showed a typical morphology of elongated tubular and short prismatic crystals. The EDS and XRD results indicated that the chemical composition of the MAP precipitates depended on the chemicals used and experimental conditions. The study confirmed that the recovery of NH4+-N from landfill leachate and seawater bitten wastes could be effectively achieved by MAP precipitation to obtain struvite crystals with a composition of 5.1%N, 10.3%Mg and 16.5%P.

Chemical Precipitation↗

PubMed2002

Photoelectrocatalytic oxidation of rhodamine B in aqueous solution using Ti/TiO2 mesh photoelectrodes.

To further improve the photooxidation techniques for water and waste-water purification, a Ti/TiO2 mesh electrode, was successfully prepared by anodizing Ti mesh in 0.5M H2SO4 solution. The structural and surface morphology of the Ti/TiO2 electrode was examined by Raman spectroscopy and scanning electronic microscopy (SEM) respectively. The examination results indicated that its structure and properties were affected by its growth rate in the anodization process, and anatase TiO2 was dominant in its composition. The photocatalytic (PC) oxidation and photoelectrocatalytic (PEC) oxidation of rhodamine B in aqueous solution using the Ti/TiO2 electrode were investigated and compared. The experimental results demonstrated that the PEC oxidation by applying an electrical bias between the Ti/TiO2 electrode and Pt electrode could significantly enhance the degradation rate of rhodamine B compared with the PC oxidation. It was found that the best performance of PEC oxidation was achieved by applying the electrical bias of 0.6 V. The mechanism of rhodamine B degradation in the PEC process was discussed by studying the changes of absorbance spectrum and proton nuclear magnetic resonance spectroscopy of rhodamine B during the PEC degradation. The experimental results illustrated that both de-ethylation and chromogen destruction of rhodamine B under UV-light irradiation in the PEC degradation took place simultaneously.

Coloring Agents↗

PubMed2001

Study of Au/Au(3+)-TiO2 photocatalysts toward visible photooxidation for water and wastewater treatment.

With an attempt to extend light absorption of TiO2-based photocatalyst toward the visible light range and eliminate the rapid recombination of excited electrons/holes during photoreaction, a new type of photocatalysts (Au/Au(3+)-TiO2) powder was prepared by a photoreduction/sol-gel process. The crystal phase composition, surface structure, and light absorption of the new photocatalysts were comprehensively examined by X-ray differential detection (XRD), UV-visible absorption spectra, X-ray photoelectron emission spectroscopy (XPS), and photoluminescence (PL) spectra. The photooxidation efficiencies of the photocatalysts were also evaluated in the photodegradation of methylene blue (MB) in aqueous solutions under visible light irradiation from a high-pressure sodium lamp (lambda > 400 nm). The results of PL analyses in this study indicated that the gold/gold ion-doping on the surface of TiO2 could eliminate the electron/holes recombination and also increase the light absorption in the visible range. The analytical results of UV-visible diffuse reflection spectra (DRS) and optical absorption spectra indicated that a new energy level below 3.2 eV generated in the Au/Au(3+)-TiO2 promoted the optical absorption in the visible region and made it possible to be excited by visible light (E < 3.2 eV). The experiment demonstrated that the photooxidation efficiency of MB using the Au/Au(3+)-TiO2 powder were significantly higher than that using conventional TiO2 powder and an optimum molar content of gold doping/deposition in the TiO2 was 0.5%. The development of such photocatalysts may be considered a breakthrough in large-scale utilization of solar energy to address environmental needs.

Air Pollutants↗

PubMed2001

Expression and potential role of angiopoietins and Tie-2 in early development of the mouse metanephros.

Angiopoietins (Ang) are secreted factors which bind the Tie-2 receptor and modulate endothelial growth. This signalling system is known to be expressed in later stages of maturation of the mouse metanephros, the adult kidney precursor. In this study, by using reverse transcription polymerase chain reaction and Northern and Western blotting, we demonstrated that Ang-1, Ang-2, and Tie-2 were expressed during early metanephrogenesis when interstitial and glomerular capillaries begin to form. By using immunohistochemistry, embryonic kidney capillaries in the interstitium and glomeruli expressed Tie-2 at a later stage of differentiation compared with vascular endothelial growth factor receptor-2 and platelet-endothelial cell adhesion molecule. Addition of 200 ng/ml Ang-1 to explanted embryonic day (E) 12.5 metanephroi increased the proportion of vascular glomeruli that formed during 1 week in culture. These results are consistent with the hypotheses that Tie-2 has a role in vascular growth in the early stages of mammalian nephrogenesis and that Tie-2 activation may maintain the integrity of recently formed interstitial and glomerular vessels.

Angiopoietin-1↗

PubMed2001

Stereoselective reduction with NADH model BNAH through chiral induction in cyclodextrins.

Stereoselective reductive debromination-cyclopropanation of 2-bromo-1-phenylethylidene-malononitrile and 2-bromo-1-beta-naphthylethylidenemalononitrile by coenzyme NADH model BNAH through chiral induction in cyclodextrins is reported. The matching between substrates and cyclodextrins, the substituent effect, and the effect of cyclodextrin concentration on the optical yields have been investigated.

Cyclodextrins↗

PubMed2001

Efficiency of biological treatment affected by high strength of ammonium-nitrogen in leachate and chemical precipitation of ammonium-nitrogen as pretreatment.

Leachate samples with a high strength of ammonium-nitrogen (NH4+-N) were collected from a local landfill site in Hong Kong. Two experiments were carried out to study (1) the inhibition of microbial activity of activated sludge by NH4+-N and (2) the chemical precipitation of NH4+-N from leachate as a preliminary treatment prior to the activated sludge process. The experimental results demonstrated that the efficiency of COD removal decreased from 97.7% to 78.1%, and the dehydrogenase activity of activated sludge decreased from 9.29 to 4.93 microg TF/mg MLSS, respectively, when the NH4+-N concentration increased from 53 to 800 mg/l. The experiment also demonstrated that the NH4+-N in the leachate can be quickly precipitated as MgNH4PO4 x 6H2O after addition of MgCl2 x 6H2O + Na2HPO4 x 12H2O. The NH4+-N concentration was reduced from 5618 to 112 mg/l within 15 min when a molar ratio of Mg2+:NH+:PO4(3-) = 1:1:1 was used. The optimum pH to reach the minimum solubility of MgNH4PO4 x 6H2O was found to be in the range of 8.5-9.0. Attention should be given to the high salinity formed in the treated leachate by using MgCl2 x 6H2O + Na2HPO4 x 12H2O, which may affect microbial activity in the following biological treatment processes. Using two other combinations of chemicals [MgO + 85%H3PO4 and Ca(H2PO4)2 x H2O + MgSO4 x 7H2O] could minimise salinity generation after precipitation, while they were less efficient for NH4+-N removal.

Hydrogen-Ion Concentration↗

PubMed2001

Further formation of trihalomethanes in drinking water during heating.

This study was aimed at investigating the further formation of trihalomethanes (THM) in drinking water when it is being heated at home. Experimental results confirmed that there could be a further significant formation during heating drinking water. Overall variation of THM concentration in water during the heating depended on its formation rate and volatilisation rate. The rate of THM formation was mainly affected by not only both the concentrations of THM precursors, such as humic substances and residual chlorine, but also temperature and reaction time. The rate of THM volatilisation depended on water temperature and the extent of water agitation in the water heaters. It was concluded that the THM residuals in drinking water could be effectively eliminated to a very low level, if the boiling of water was kept in the open for few minutes after water boiling.

Temperature↗