Ceria-based supported noble-metal catalysts release oxygen, which may help to reduce the formation of carbonaceous residues, for example during hydrocarbon reforming. To gain insight into the microscopic origins of these effects, a model study is performed under ultrahigh-vacuum conditions using single-crystal-based supported model catalysts. The model systems are based on ordered CeO(2)(111) films on Cu(111), on which Pt nanoparticles are grown by physical vapor deposition. The growth and structure of the surfaces are characterized by means of scanning tunneling microscopy, and the electronic structure and reactivity are probed by X-ray photoelectron spectroscopy. Specifically, it is shown that the fully oxidized CeO(2) thin films undergo slight reduction upon Pt deposition (CeO(1.99)). This effect is enhanced upon annealing (CeO(1.96)), thus indicating facile oxygen release and reverse spillover. The model system is structurally stable up to temperatures exceeding 700 K. The activation of methane is investigated using high-kinetic-energy CH(4) (0.83 eV), generated by a supersonic molecular beam. It is shown that dehydrogenation occurs under rapid formation of CH or C species without detectable amounts of CH(3) being formed, even at low temperatures (100 K). The released hydrogen spills over to the CeO(2) support, which leads to the formation of OH groups. At 200 K and above, the OH groups start to decompose leaving additional Ce(3+) centers behind (CeO(1.97-1.94)). At up to 700 K, carbon deposits are quantitatively removed by reaction with oxygen, which is supplied by reverse spillover from the CeO(2) film, thus leading to substantial reduction of the support (approximately CeO(1.90-1.85)).

Developing low-temperature deNOx catalysts with high catalytic activity, SO2-tolerance and stability is highly desirable but remains challenging. Herein, by coating the mesoporous TiO2 layers on carbon nanotubes (CNTs)-supported MnOx and CeOx nanoparticles (NPs), we obtained a core-shell structural deNOx catalyst with high catalytic activity, good SO2-tolerance and enhanced stability. Transmission electron microscopy, X-ray diffraction, N2 sorption, X-ray photoelectron spectroscopy, H2 temperature-programmed reduction and NH3 temperature-programmed desorption have been used to elucidate the structure and surface properties of the obtained catalysts. Both the specific surface area and chemisorbed oxygen species are enhanced by the coating of meso-TiO2 sheaths. The meso-TiO2 sheaths not only enhance the acid strength but also raise acid amounts. Moreover, there is a strong interaction among the manganese oxide, cerium oxide and meso-TiO2 sheaths. Based on these favorable properties, the meso-TiO2 coated catalyst exhibits a higher activity and more extensive operating-temperature window, compared to the uncoated catalyst. In addition, the meso-TiO2 sheaths can serve as an effective barrier to prevent the aggregation of metal oxide NPs during stability testing. As a result, the meso-TiO2 overcoated catalyst exhibits a much better stability than the uncoated one. More importantly, the meso-TiO2 sheaths can not only prevent the generation of ammonium sulfate species from blocking the active sites but also inhibit the formation of manganese sulfate, resulting in a higher SO2-tolerance. These results indicate that the design of a core-shell structure is effective to promote the performance of deNOx catalysts.

The present XANES study aims at elucidating the roles of carbon deposits and metal sulfides in the catalyst deactivation in steam reforming reactions with the presence of sulfur. CeO(2)-Al(2)O(3)-supported Ni and Rh-based catalysts were tested in steam reforming of liquid hydrocarbon fuel containing 350 ppm sulfur for H(2) production at 800 degrees C. The Rh catalyst demonstrated much better sulfur tolerance than the Ni catalyst. XANES revealed that there are various sulfur species (metal sulfide, sulfonate, sulfate and organic sulfide) on the used Ni and Rh catalysts. Metal sulfide and organic sulfide are the dominant sulfur species on the Ni catalyst whereas sulfonate and sulfate predominate on the Rh catalyst. Meanwhile organic sulfide and sulfate are also observed on the support alone. Furthermore, there are more carbon deposits formed in the presence of sulfur on both catalysts. More carboxyl groups occur on the carbon deposits formed on the same catalyst when there is no sulfur in the fuel. From correlation analysis of the amounts of nickel sulfide and carbon deposits along with the relative catalytic activity loss, we conclude that sulfur causes the initial deactivation of the Ni catalyst by metal sulfide formation in the first few hours while build-up of carbon deposits contributes mainly to the subsequent deactivation.

Because of growing environmental concerns and increasingly stringent regulations governing auto emissions, new more efficient exhaust catalysts are needed to reduce the amount of pollutants released from internal combustion engines. To accomplish this goal, the major pollutants in exhaust-CO, NO(x), and unburned hydrocarbons-need to be fully converted to CO(2), N(2), and H(2)O. Most exhaust catalysts contain nanocrystalline noble metals (Pt, Pd, Rh) dispersed on oxide supports such as Al(2)O(3) or SiO(2) promoted by CeO(2). However, in conventional catalysts, only the surface atoms of the noble metal particles serve as adsorption sites, and even in 4-6 nm metal particles, only 1/4 to 1/5 of the total noble metal atoms are utilized for catalytic conversion. The complete dispersion of noble metals can be achieved only as ions within an oxide support. In this Account, we describe a novel solution to this dispersion problem: a new solution combustion method for synthesizing dispersed noble metal ionic catalysts. We have synthesized nanocrystalline, single-phase Ce(1-x)M(x)O(2-delta) and Ce(1-x-y)Ti(y)M(x)O(2-delta) (M = Pt, Pd, Rh; x = 0.01-0.02, delta approximately x, y = 0.15-0.25) oxides in fluorite structure. In these oxide catalysts, Pt(2+), Pd(2+), or Rh(3+) ions are substituted only to the extent of 1-2% of Ce(4+) ion. Lower-valent noble metal ion substitution in CeO(2) creates oxygen vacancies. Reducing molecules (CO, H(2), NH(3)) are adsorbed onto electron-deficient noble metal ions, while oxidizing (O(2), NO) molecules are absorbed onto electron-rich oxide ion vacancy sites. The rates of CO and hydrocarbon oxidation and NO(x) reduction (with >80% N(2) selectivity) are 15-30 times higher in the presence of these ionic catalysts than when the same amount of noble metal loaded on an oxide support is used. Catalysts with palladium ion dispersed in CeO(2) or Ce(1-x)Ti(x)O(2) were far superior to Pt or Rh ionic catalysts. Therefore, we have demonstrated that the more expensive Pt and Rh metals are not necessary in exhaust catalysts. We have also grown these nanocrystalline ionic catalysts on ceramic cordierite and have reproduced the results we observed in powder material on the honeycomb catalytic converter. Oxygen in a CeO(2) lattice is activated by the substitution of Ti ion, as well as noble metal ions. Because this substitution creates longer Ti-O and M-O bonds relative to the average Ce-O bond within the lattice, the materials facilitate high oxygen storage and release. The interaction among M(0)/M(n+), Ce(4+)/Ce(3+), and Ti(4+)/Ti(3+) redox couples leads to the promoting action of CeO(2), activation of lattice oxygen and high oxygen storage capacity, metal support interaction, and high rates of catalytic activity in exhaust catalysis.

Cerium oxide cluster cations (Ce(m)O(n)(+), m = 2-16; n = 2m, 2m +/- 1 and 2m +/- 2) are prepared by laser ablation and reacted with carbon monoxide (CO) and small hydrocarbon molecules (CH(4), C(2)H(4), and C(2)H(6)) in a fast flow reactor. A time of flight mass spectrometer is used to detect the cluster distribution before and after the reactions. The observation of oxygen reduction and hydrogen pickup of Ce(m)O(2m)(+) clusters strongly suggests the following reactions: (1) Ce(m)O(2m)(+) + C(2)H(4) ->> Ce(m)O(2m-1)(+) + C(2)H(4)O (m = 2-6); (2) Ce(m)O(2m)(+) + CO ->> Ce(m)O(2m-1)(+) + CO(2) (m = 4-6); and (3) Ce(m)O(2m)(+) + CH(4)/C(2)H(6) ->> Ce(m)O(2m)H(+) + CH(3)/C(2)H(5) (m = 2-4). Density functional theory (DFT) calculations are performed to study reaction mechanisms of Ce(2)O(4)(+) + X (X = CO, CH(4), C(2)H(4), and C(2)H(6)). The calculated results are in good agreement with the experimental observations. The structural and bonding properties of Ce(m)O(2m)(+) (m = 2-5) clusters are also investigated by the DFT calculations. The unpaired electron in each of the clusters is mainly distributed over one Ce atom (4f and 5p orbitals) and two O atoms (2p orbital) in a CeO(2) moiety, which can be considered as the active site in the cluster. To further understand the nature of the active sites in Ce(m)O(2m)(+) clusters, the fast flow reaction experiments are also carried out on zirconium oxide clusters Zr(m)O(n)(+), because both Zr ([Kr]4d(2)5s(2)) and Ce ([Xe]4f(1)5d(1)6s(2)) have the same number of valence electrons while the latter has one more f and one less d electrons. In addition to the oxygen transfer reactions such as Zr(m)O(2m)(+) + C(2)H(4) ->> Zr(m)O(2m-1)(+) + C(2)H(4)O (m = 1-4) reported in the literature, hydrogen abstraction reactions Zr(m)O(2m)(+) + CH(4)/C(2)H(6) ->> Zr(m)O(2m)H(+) + CH(3)/C(2)H(5) are also identified. The rate constants of CO oxidation as well as hydrogen abstraction by Ce(m)O(2m)(+) and Zr(m)O(2m)(+) are very different. The reactivity and selectivity of Ce(m)O(2m)(+) versus Zr(m)O(2m)(+) can be well rationalized based on the DFT calculations. The oxygen transfer and hydrogen abstraction reactions studied in this work are of widespread importance. The nature of the active sites of Ce(m)O(2m)(+) clusters is unique and may be considered in the use and design of cerium oxide based catalysts.

BACKGROUND

To estimate the magnitude and causes of blindness and vision impairment in Papua New Guinea for service delivery planning and ophthalmic education development.

METHODS

Using the World Health Organization standardized Rapid Assessment of Cataract Surgical Services protocol, a population-based cross-sectional survey was conducted in 2005. By systematic, two-stage cluster random sampling, 39 clusters each of 30 people aged 50 years and over were selected from urban and rural locations. A cause of vision loss was determined for each eye with a presenting visual acuity worse than 6/18.

RESULTS

Of the 1191 people enumerated, 1174 were examined (98.6%). The 50 years and older age-gender adjusted prevalence of vision impairment (presenting visual acuity less than 6/18 in the better eye) was 29.2% (95% Confidence Interval [CI]: 27.6, 35.1, Design Effect [deff] = 2.3). That of functional blindness (presenting visual acuity less than 6/60 in the better eye) was 8.9% (95% CI: 8.4, 12.0, deff = 1.2), and of World Health Organization blindness (but presenting, rather than best corrected, visual acuity of less than 3/60 in the better eye) was 3.9% (95% CI: 3.4, 6.1, deff = 1.0). Uncorrected refractive error (13.1%, 95% CI: 11.3, 15.1, deff = 1.2) and cataract (7.4%, 95% CI: 6.4, 10.2, deff = 1.3) were leading causes of vision impairment, age-gender adjusted. Cataract was the most common (age-gender adjusted 6.4%, 95% CI: 5.1, 7.3, deff = 1.1) cause of functional blindness. On bivariate analysis, increasing age (P < 0.001), illiteracy (P < 0.001) and unemployment (P < 0.001) were associated with functional blindness. Gender was not.

CONCLUSIONS

The identification and treatment of refractive error and cataract need to be priorities for eye health services in Papua New Guinea if the burden of vision impairment and blindness is to be diminished. The education of community and hospital eye care providers, whether medical, nursing or other cadres, must emphasize these. Eye care services must be structured and provided to allow and encourage accessibility and uptake, with satisfactory treatment outcomes for these conditions.

BACKGROUND

To describe self-reported patterns of care for glaucoma of ophthalmologists in Australia and New Zealand and summarize current practice styles and patterns associated with glaucoma management.

METHODS

A questionnaire of glaucoma management practices was mailed to all ophthalmologists registered with the Royal Australian and New Zealand College of Ophthalmologists in June 2003. The questionnaire assessed practice preferences for medical management, examination techniques and indications for surgery. The results were cross-tabulated by age, country and subspecialty training in glaucoma.

RESULTS

Fifty-one per cent of 761 surveys were returned, 14% being from glaucoma specialists. New Zealand ophthalmologists proceeded to surgical management of glaucoma earlier than did their Australian colleagues. Australian ophthalmologists tended to use argon laser trabeculoplasty more frequently. Ninety-six per cent of ophthalmologists routinely use gonioscopy in diagnosing glaucoma. Disc drawings and recording cup:disc ratios were the most commonly used methods of documenting disc morphology; glaucoma specialists were more likely to use imaging technologies. SITA-Standard 24-2 was the most commonly used modality of perimetry, and was favoured by glaucoma specialists.

CONCLUSIONS

This survey represents the first Australian and New Zealand effort to identify glaucoma management practices. Although a substantial consensus was found in most areas of treatment, a few areas showed diversity. The information gathered will enable ophthalmologists to compare their own practices with those of their colleagues. In addition, this survey provides a baseline allowing future trends in management to be determined.

A quantitative method based on UV-vis diffuse reflectance spectroscopy (DRS) was developed that allows determination of the fraction of monomeric and polymeric VO(x) species that are present in vanadate materials. This new quantitative method allows determination of the distribution of monomeric and polymeric surface VO(x) species present in dehydrated supported V(2)O(5)/SiO(2), V(2)O(5)/Al(2)O(3), and V(2)O(5)/ZrO(2) catalysts below monolayer surface coverage when V(2)O(5) nanoparticles are not present. Isolated surface VO(x) species are exclusively present at low surface vanadia coverage on all the dehydrated oxide supports. However, polymeric surface VO(x) species are also present on the dehydrated Al(2)O(3) and ZrO(2) supports at intermediate surface coverage and the polymeric chains are the dominant surface vanadia species at monolayer surface coverage. The propane oxidative dehydrogenation (ODH) turnover frequency (TOF) values are essentially indistinguishable for the isolated and polymeric surface VO(x) species on the same oxide support, and are also not affected by the Brønsted acidity or reducibility of the surface VO(x) species. The propane ODH TOF, however, varies by more than an order of magnitude with the specific oxide support (ZrO(2)>> Al(2)O(3)>>) SiO(2)) for both the isolated and polymeric surface VO(x) species. These new findings reveal that the support cation is a potent ligand that directly influences the reactivity of the bridging V-O-support bond, the catalytic active site, by controlling its basic character with the support electronegativity. These new fundamental insights about polymerization extent of surface vanadia species on SiO(2), Al(2)O(3), and ZrO(2) are also applicable to other supported vanadia catalysts (e.g., CeO(2), TiO(2), Nb(2)O(5)) as well as other supported metal oxide (e.g., CrO(3), MoO(3), WO(3)) catalyst systems.

In this work, cerium oxide nanoparticles are capable of strongly enhancing the chemiluminescence (CL) of the luminol-hydrogen peroxide (H2O2) system. Based on this, a microarray CL method for the determination of the removal rate constant of H2O2 by human erythrocytes has been developed. It is providing direct evidence for a H2O2-removing enzyme in human erythrocytes that acts as the predominant catalyst. A reaction mechanism is discussed. The proposed microarray CL method is sensitive, selective, simple and time-saving, and has good reproducibility and high throughput. Relative CL intensity is linearly related to the concentration of H2O2 in the range from 0.01 to 50 μM. The limit of detection is as low as 6.5 × 10(-11) M (3σ), and the relative standard deviation is 2. 1 % at 1 μM levels of H2O2 (for n = 11).

This work investigated the effect of several metal oxides including alpha-FeOOH, alpha-Fe(2)O(3), gamma-FeOOH, and CeO(2) on bromate formation potential (BFP) during ozonation of bromide-containing water. Results indicate that CeO(2) could most effectively minimize the BFP among these metal oxides taking ozonation alone as control. The BFP minimization by O(3)/CeO(2) favored a relatively low Br(-) concentration (i.e., <1.0mgL(-1)) and pH<7. Water temperature ranging from 5 to 25 degrees C had no significant impact on the percent reduction of BrO(3)(-). Further investigation indicates that the effective BFP minimization can be ascribed to neither the surface adsorption of BrO(3)(-) or Br(-) on CeO(2) nor the surface reduction of BrO(3)(-) to HOBr/OBr(-) by CeO(2). It seems to have relationship with the activity of surface Ce(IV) sites. The CeO(2) can lower the concentration of H(2)O(2) which is formed during ozone decomposition and promotes BrO(3)(-) formation. Another possible reason for the BFP minimization is that the CeO(2) could possibly reduce BrO() to HOBr/OBr(-) during the decomposition of H(2)O(2).

Cerium (Ce)-based compounds, such as CeO₂ nanoparticles (NPs), have received much attention in the last several years due to their popular applications in industrial and commercial uses. Understanding the impact of CeO₂ NPs on nutrient cycles, a subchronic toxicity study of CeO₂ NPs on soil-denitrification process was performed as a function of particle size (33 and 78 nm), total Ce concentration (50-500 mg L(-1)), and speciation [Ce(IV) vs. Ce(III)]. The antimicrobial effect on the soil-denitrification process was evaluated in both steady-state and zero-order kinetic models to assess particle- and chemical-species specific toxicity. It was found that soluble Ce(III) was far more toxic than Ce(IV)O₂ NPs when an equal total concentration of Ce was evaluated. Particle size-dependent toxicity, species-dependent toxicity, and concentration-dependent toxicity were all observed in this study for both the steady-state and the kinetic evaluations. Changes in physicochemical properties of Ce(IV)O₂ NPs might be important in assessing the environmental fate and toxicity of NPs in aquatic and terrestrial environments.

High-throughput continuous hydrothermal flow synthesis has been used as a rapid and efficient synthetic route to produce a range of crystalline nanopowders in the Ce-Zn oxide binary system. High-resolution powder X-ray diffraction data were obtained for both as-prepared and heat-treated (850 degrees C for 10 h in air) samples using the new robotic beamline I11, located at Diamond Light Source. The influence of the sample composition on the crystal structure and on the optical and physical properties was studied. All the nanomaterials were characterized using Raman spectroscopy, UV-visible spectrophotometry, Brunauer-Emmett-Teller surface area and elemental analysis (via energy-dispersive X-ray spectroscopy). Initially, for 'as-prepared' Ce(1-x)Zn(x)O(y), a phase-pure cerium oxide (fluorite) structure was obtained for nominal values of x=0.1 and 0.2. Biphasic mixtures were obtained for nominal values of x in the range of 0.3-0.9 (inclusive). High-resolution transmission electron microscopy images revealed that the phase-pure nano-CeO(2) (x=0) consisted of ca 3.7 nm well-defined nanoparticles. The nanomaterials produced herein generally had high surface areas (greater than 150 m(2) g(-1)) and possessed combinations of particle properties (e.g. bandgap, crystallinity, size, etc.) that were unobtainable or difficult to achieve by other more conventional synthetic methods.

Cultural changes are needed in medicine if the benefits of technological advances are to benefit healthcare users. The Digital Health Manifesto of 'medical futurist' doctor Bertalan Meskó and 'e-patient' Dave deBronkart, The Patient Will See You Now by Eric Topol and The Patient as CEO by Robin Farmanfarmaian, are among the proliferating warnings of the approaching paradigm shift in medicine, resulting, above all, from technological advances that gives users independent access to exponentially increasing amounts of information about themselves. We question their messages only in suggesting they do not sufficiently shift the focus from 'patient' to 'person' and consequently fail to recognise the need for the credible, efficient, ethical and independent decision support that can ensure the 'democratisation of knowledge' is person empowering, not overpowering. Such decision support can ensure the 'democratisation of decision,' leading to higher quality decisions and fully-informed and preference-based consent to health provider actions. The coming paradigm will therefore be characterised by apomediative ('direct-to-consumer') decision support tools, engaged with by the person in the community to help them make health production decisions for themselves (including whether to consult a healthcare professional or provider), as well as intermediative ('direct-from-clinician') tools, delivered by a health professional in a 'shared decision making' or 'co-creation of health' process. This vision paper elaborates on the implementation of these preference-sensitive decision support tools through the technique of Multi-Criteria Decision Analysis.

The cytocompatibility of potential bioactive cerium-containing (Ce³⁺/Ce⁴⁺) glasses is here investigated by preparing three different glasses with increasing amount of doping CeO₂ (1.2, 3.6 and 5.3 mol% of CeO₂, called BG_1.2, BG_3.6 and BG_5.3, respectively) based on 45S5 Bioglass® (called BG). These materials were characterized by Environmental Scanning Electron Microscopy (ESEM) and infrared spectroscopy (FTIR) after performing bioactivity tests in Dulbecco's Modified Eagle Medium (DMEM) solution, and the ions released in solution were determined by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Optical Emission Spectrometry (ICP-OES). The data obtained clearly show that the glass surfaces of BG, BG_1.2 and BG_3.6 were covered by hydroxyapatite (HA), while BG_5.3 favored the formation of a cerium phosphate crystal phase. The cytotoxicity tests were performed using both murine long bone osteocyte-like (MLO-Y4) and mouse embryonic fibroblast (NIH/3T3) cell lines. The cerium-containing bioactive glasses show an increment in cell viability with respect to BG, and at long times, no cell aggregation and deformation were observed. The proliferation of NIH/3T3 cells increased with the cerium content in the glasses; in particular, BG_3.6 and BG_5.3 showed a higher proliferation of cells than the negative control. These results highlight and enforce the proposal of cerium-doped bioactive glasses as a new class of biomaterials for hard-tissue applications.

Rod and sphere-like CeO(2) particles were obtained via a supercritical solvothermal method using CeCl(3).7H(2)O and Ce(NO(3))(3).6H(2)O as cerium sources in ethanol and methanol at 400 degrees C for 15 min followed by calcination in air. The rodlike particles were 200-400 nm in diameter and 1-2 mum in length. The spherical particles were 300-500 nm in diameter. The as-prepared rodlike particles using CeCl(3).7H(2)O consisted of mixtures of Ce(OH)(3) and Ce(CH(3)COO)(3) and were converted to rodlike CeO(2) by calcination in air at 500 degrees C. In contrast, the spherical particles prepared using Ce(NO(3))(3).6H(2)O consisted of fluorite-structured CeO(2). The possible formation mechanism was discussed on the basis of the effect of reaction time on the morphology at 400 degrees C. The rod- and spherelike CeO(2) particles exhibited strong UV absorption below 400 nm, and the absorbance edges extend to nearly 500 nm. The rod- and spherelike CeO(2) particles exhibited near-UV emission at 360 nm and blue emission at 465 nm with higher emission intensity compared to the commercial CeO(2) sample.

An efficient and simple method for enrichment and identification of phosphopeptides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) using cerium oxide is presented. After pretreatment of tryptic digests of phosphoproteins with CeO(2), nonphosphopeptides are discarded and phosphopeptides are enriched. By applying the separated CeO(2) on a target plate and analysis using MALDI-TOF MS, peaks of phosphopeptides and their correspondingly series of dephosphorylated peptides are observed in the mass spectra. Thus, the phosphopeptides are very easy to identify with the mass difference, which are all 80 Da between adjacent peaks in the same series, and clear background in the spectra owing to elimination of signal suppression from large amounts of nonphosphopeptides. Furthermore, the phosphopeptides can be dephosphorylated completely after a further NH(4)OH elution. Tryptic digest products from several standard proteins are pretreated using CeO(2) to demonstrate the efficiency of this method. Phosphopeptides from a very small quantity of human serum are enriched and analyzed, and proteins also identified by searching against a database using Mascot on MALDI-TOF/TOF fragments, which indicates that this method may be employed in complex samples for further application.

Gd-doped CeO(2) exhibits an anomalously large electrostriction effect generating stress that can reach 500 MPa. In situ XANES measurements indicate that the stress develops in response to the rearrangement of cerium-oxygen vacancy pairs. This mechanism is fundamentally different from that of materials currently in use and suggests that Gd-doped ceria is a representative of a new family of high-performance electromechanical materials.

Copper oxide (CuO)-decorated cerium oxide (CeO₂) nanoparticles were synthesized and used to detect glucose non-enzymatically. The morphological characteristics and structure of the nanoparticles were characterized through transmission electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. The sensor responses of electrodes to glucose were investigated via an electrochemical method. The CuO/CeO₂ nanocomposite exhibited a reasonably good sensitivity of 2.77 μA mM-1cm-2, an estimated detection limit of 10 μA, and a good anti-interference ability. The sensor was also fairly stable under ambient conditions.

We introduce a new concept for a nanomaterial in terms of both synthesis and properties. The nanomaterial, aggregates of ceria particles around central silver metal (CeO(2)-Ag), was fabricated by a one-pot selective redox reaction using cerium(III) and silver(I) autocatalyzed by silver metal without the need for surfactants or organic compounds. This unique nanostructure is suitable as a catalyst, in contrast to core-shell materials wherein the shell deactivates the catalyst metal. The material was developed to be intimately related to catalytic carbon oxidation.

The interaction of Pt with CeO(2) layers was investigated by using photoelectron spectroscopy. The 30 nm thick Pt doped CeO(2) layers were deposited simultaneously by rf-magnetron sputtering on a Si(001) substrate, multiwall carbon nanotubes (CNTs) supported by a carbon diffusion layer of a polymer membrane fuel cell and on CNTs grown on the silicon wafer by the CVD technique. The synchrotron radiation X-ray photoelectron spectra showed the formation of cerium oxide with completely ionized Pt(2+,4+) species, and with the Pt(2+)/Pt(4+) ratio strongly dependent on the substrate. The TEM and XRD study showed the Pt(2+)/Pt(4+) ratio is dependent on the film structure.

Maternal infection with rubella in the first trimester is an important cause of congenital cataract. Any injury affecting the foetus following maternal rubella infection in the phase of organogenesis results in congenital defects collectively termed as congenital rubella syndrome (CRS). Although rubella embryopathy is a less common cause for congenital cataract than in the past, it is still seen. The number of cases reduced to one in 1997 after which there were no new cases till 2002. However, there have been two new cases of CRS in 2003. Herein another one in early 2004 is reported. Outbreaks of CRS will continue until the percentage of susceptible individuals is reduced to a minimum through immunization. The majority of rubella cases in Australia are confined to young female immigrants, many coming for marriage. We must continue to immunize children, identify and immunize vaccine failures and susceptible women before they become pregnant, and to screen pregnant women so they can be vaccinated after delivery.

Rob Burns talks with Dane Miller, former CEO of Biomet, about challenges posed by new technology in the orthopedic devices area. One key challenge is the rising cost and use of orthopedic devices at a time when providers are facing decreased profitability and reimbursement for orthopedic services. Another challenge is the long-term time horizon needed to gauge product success that contrasts with payers' and providers' short-term horizon. A third challenge is heightened governmental scrutiny of device makers' relationships with orthopedic surgeons. This interview was conducted before Miller left Biomet in March 2006.

Uniform CeO(2) nanoflowers were synthesized by rapid thermolysis of (NH(4))(2)Ce(NO(3))(6) in oleic acid (OA)/oleylamine (OM), by a unique 3D oriented-attachment mechanism. CeO(2) nanoflowers with controlled shape (cubic, four-petaled, and starlike) and tunable size (10-40 nm) were obtained by adjusting the reaction conditions including solvent composition, precursor concentration, reaction temperature, and reaction time. The nanoflower growth mechanism was investigated by in situ electrical conductance measurements, transmission electron microscopy, and UV/Vis spectroscopy. The CeO(2) nanoflowers are likely formed in two major steps, that is, initial formation of ceria cluster particles capped with various ligands (e.g., OA, OM, and NO(3) (-)) via hydrolysis of (NH(4))(2)Ce(NO(3))(6) at temperatures in the range 140-220 degrees C, and subsequent spontaneous organization of the primary particles into nanoflowers by 3D oriented attachment, due to a rapid decrease in surface ligand coverage caused by sudden decomposition of the precursor at temperatures above 220 degrees C in a strong redox reaction. After calcination at 400 degrees C for 4 h the 33.8 nm CeO(2) nanoflowers have a specific surface area as large as 156 m(2) g(-1) with high porosity, and they are highly active for conversion of CO to CO(2) in the low temperature range of 200-400 degrees C. The present approach has also been extended to the preparation of other transition metal oxide (CoO, NiO, and CuO(x)) nanoflowers.

Sr(2)CeO(4) and Sr(2)CeO(4):Eu(3+),Dy(3+) phosphor particles and thin films were prepared by using an emulsion liquid membrane (ELM, water-in-oil-in-water (W/O/W) emulsion) system, containing VA-10 (2-methyl-2-ethylheptanoic acid) as extractant (cation carrier). A two-step extraction enabled efficient extraction for Sr(3+) and rare earth ions, and the resulting precursor metal oxalate particles produced in the internal water phase of the ELM system were about 60 nm in diameter. Calcination of the oxalate particles in air gave submicrometer-sized Sr(2)CeO(4) and Sr(2)CeO(4):Eu(3+),Dy(3+) particles, which showed blue and white luminescence, respectively, by UV excitation. Blue and white luminescence phosphor thin films were also prepared by soaking alumina substrates into the W/O emulsion containing precursor oxalate particles, followed by calcination in air.