45,883 research outputs found
Letter dated 9 April 1969 from Sterling J. Richards to T. J. Marshall
Letter dated 9 April 1969 from Sterling J. Richards, Professor of Soil Physics at the University of California at Riverside, to T. J. Marshall of Berkeley, California, offering to make advance arrangements before latter\u27s visit to the Riverside campusUNIVERSITY OF CALIFORNIA, RIVERSIDE BERKELEY • DAVIS • IRVINE • LOS ANGELES • RIVERSIDE • SAN DIEGO • SAN FRANCISCO > COLLEGE OF BIOLOGICAL AND AGRICULTURAL SCIENCES CITRUS RESEARCH CENTER AND AGRICULTURAL EXPERIM ENT STATION DEPARTMENT OF SOILS AND PLANT NUTRITION SANTA BARBARA • SANTA CRUZ A Tribute to the People of California RIVERSIDE, CALIFORNIA 92502 April 9, 1969 Dr* t. J. Marshall c/o Mra. J. Grow* 1827 Catalina Avenue Berkeley* California §4?©? Eear Xi»j I was pUmmd to learn that you were planning *© spend Thursday, April 24, on our cafapus. i have mentioned your coming to several a ^ will confirm it liy sending the® copies of this latter* If thare are advance arrangements for you end Mrs. Marshall for things you would cars to aaa or do, i should fe® glad to ha helpful. W© are definitely looking forward to a visit with you. Sincerely. Sterling. J. Eichards frefesser of Soil Physios $Jit?dem eei F* F, Pratt Ii* 8, Stolsy L. A, aichnrds J. tete
Measurement of the ratio of prompt χ c to J / ψ production in pp collisions at √s = 7 TeV
The prompt production of charmonium χ c and J / ψ states is studied in proton-proton collisions at a centre-of-mass energy of √s = 7 TeV at the Large Hadron Collider. The χ c and J / ψ mesons are identified through their decays χ c → J / ψ γ and J / ψ → μ + μ - using 36 pb - 1 of data collected by the LHCb detector in 2010. The ratio of the prompt production cross-sections for χ c and J / ψ, σ (χ c → J / ψ γ) / σ (J / ψ), is determined as a function of the J / ψ transverse momentum in the range 2 < p T J / ψ < 15 GeV / c. The results are in excellent agreement with next-to-leading order non-relativistic expectations and show a significant discrepancy compared with the colour singlet model prediction at leading order, especially in the low p T J / ψ region
Development of new proton conducting materials for intermediate temperature fuel cells
The work in this thesis mainly focuses on the preparation and characterization of several phosphates and solid oxide systems with the aim of developing new proton conducting materials for intermediate temperature fuel cells (ITFCs). Soft chemical methods such as sol-gel methods and conventional solid state methods were applied for the synthesis of these materials.
Aluminum phosphate obtained by a solution method is single phase and belongs to one of the Al(H₂PO₄)₃ allotropies with hexagonal symmetry. The material is stable up to 200°C and decomposes into Al(PO₃)₃ at a higher temperature. The electrical conductivity of pure Al(H₂PO₄)₃ is on the order of 10⁻⁶-10⁻⁷ S/cm, very close to the value for the known proton conductors AlH₃(PO₄)₂•3H₂O and AlH₂P₃O₁₀•2H₂O. Much higher conductivity is observed for samples containing even a trace amount of excess H₃PO₄. It is likely that the conduction path gradually changes from grain interior to the surface as the acid content increases. The conductivity of Al(H₂PO₄)₃-0.5H₃PO₄ exhibited a good stability over the measured 110 hours.
Although tin pyrophosphate (SnP₂O₇) has been reported to show a significantly high conductivity (~10⁻² S/cm) at 250°C in various atmospheres, we observed large discrepancies in the electrical properties of SnP₂O₇ prepared by different methods. Using an excess amount of phosphorous in the synthetic procedure generally produces SnP₂O₇ with much higher conductivity (several orders of magnitude higher) than samples with stoichiometric Sn:P ratios in their synthetic procedure. Solid state ³¹P NMR confirmed the presence of residual phosphoric acid for samples with excess starting phosphorous. Transmission Electron Microscope (TEM) confirmed an amorphous layer covered the SnP₂O₇ granules which was probably phosphoric acid or condensed phases. Thereby, it is quite likely that the high conductivity of SnP₂O₇ results mainly from the contribution of the residual acid. The conductivity of these samples exhibited a good stability over the measured 80 hours.
Based on the observations for SnP₂O₇, we developed a nano core-shell structure based on BPO₄ and P₂O₅ synthesised by solid state methods. The particle size of BPO₄ using this method varied between 10-20 nm depending on the content of P₂O₅. TEM confirmed the existence of an amorphous layer that is homogeneously distributed. The composite exhibits the highest conductivity of 8.8×10⁻² S/cm at 300°C in air for 20% extra P₂O₅ and demonstrates a good stability during the whole measured 110 hours. Polytetrafluoroethylene (PTFE) was introduced into the composites in order to increase malleability for fabrication. The conductivity and mechanical strength were optimized by adjusting the PTFE and P₂O₅ content. These organic-inorganic composites demonstrate much better stability at elevated temperature (250°C) over
conventional SiC-H₃PO₄-PTFE composites which are common electrolytes for phosphoric acid fuel cells (PAFCs). Fuel cells based on BPO₄-H₃PO₄-PTFE composite as the electrolyte were investigated using pure H₂ and methanol as fuels. A maximum power density of 320 mW/cm² at a voltage of 0.31 V and a maximum current density of 1.9 A/cm² at 200°C were observed for H₂/O₂ fuel cells. A maximum power density of 40 mW/cm² and maximum current of 300 mA/cm² 275°C were observed when 3M methanol was used in the cell.
Phosphoric acid was also introduced into materials with internal open structures such as phosphotungstic acid (H₃PW₁₂O₄₀) and heteropolyacid salt ((NH₄)₃PW₁₂O₄₀), for the purpose of acquiring additional connections. The hybrids obtained have a cubic symmetry with enlarged unit cell volume, probably due to the incorporation of phosphoric acid into the internal structures. Solid state ³¹P NMR performed on H₃PW₁₂O₄₀-xH₃PO₄ (x = 0-3) showed additional peaks at high acid content which could not assigned to phosphorus from the starting materials, suggesting a strong interaction between H₃PW₁₂O₄₀ and H₃PO₄. The conductivity of hybrids was improved significantly compared with samples without phosphoric acid. Fourier transform infrared spectra (FT-IR) suggest the existence of large amount of hydrogen bonds (OH••••O) that may responsible for the high conductivity. A H₂/O₂ fuel cell based on H₃PW₁₂O₄₀-H₃PO₄-PTFE exhibited a peak power density of 2.7 mW/cm² at 0.3 V in ambient temperature.
Solid oxide proton conductors based on yttrium doped BaZrO₃ were investigated by introducing potassium or lanthanum at the A-sites. The materials were prepared by different methods and were obtained as a single phase with space group Pm-3m (221). The unit cell of these samples is slightly smaller than the undoped one. The upper limit of solid solution formation on the A-sites for potassium is between 5 ~ 10% as introducing more K results in the occurrence of a second phase or impurities such as YSZ (yttrium stabilized zirconium). K doped Barium zirconates showed an improved water uptake capability even with 5% K doping, whereas for La doped ones, water uptake is strongly dependent on particle size and synthetic history. The conductivity of K doped BaZrO₃ was improved by a factor of two (2×10⁻³ S/cm) at 600°C compared with undoped material. Fuel cells based on Pt/Ba₀.₉₅K₀.₀₅Zr₀.₈₅Y₀.₁₁Zn₀.₀₄O[subscript(3-δ)]/Pt under humidified 5% H₂/air conditions gave a maximum power density 7.7 mWcm⁻² at 718°C and an interfacial resistance 4 Ωcm⁻². While for La doped samples, the conductivity was comparable with undoped ones; the benefits of introducing lanthanum at A-sites may not be so obvious as deficiency of barium is one factor that leads to the diminishing conductivity
Evidence for the decay B0→J/ψω and measurement of the relative branching fractions of meson decays to J/ψη and J/ψη′
First evidence of the B 0 → J / ψ ω decay is found and the B s 0 → J / ψ η and B s 0 → J / ψ η ′ decays are studied using a dataset corresponding to an integrated luminosity of 1.0 fb -1 collected by the LHCb experiment in proton-proton collisions at a centre-of-mass energy of sqrt(s) = 7 TeV. The branching fractions of these decays are measured relative to that of the B 0 → J / ψ ρ 0 decay:frac(B (B 0 → J / ψ ω), B (B 0 → J / ψ ρ 0)) = 0.89 ± 0.19 (stat) - 0.13 + 0.07 (syst),frac(B (B s 0 → J / ψ η), B (B 0 → J / ψ ρ 0)) = 14.0 ± 1.2 (stat) - 1.5 + 1.1 (syst) - 1.0 + 1.1 (frac(f d, f s)),frac(B (B s 0 → J / ψ η ′), B (B 0 → J / ψ ρ 0)) = 12.7 ± 1.1 (stat) - 1.3 + 0.5 (syst) - 0.9 + 1.0 (frac(f d, f s)), where the last uncertainty is due to the knowledge of f d / f s, the ratio of b-quark hadronization factors that accounts for the different production rate of B 0 and B s 0 mesons. The ratio of the branching fractions of B s 0 → J / ψ η ′ and B s 0 → J / ψ η decays is measured to befrac(B (B s 0 → J / ψ η ′), B (B s 0 → J / ψ η)) = 0.90 ± 0.09 (stat) - 0.02 + 0.06 (syst)
Lifetime affordable housing in Australia - assessing life-cycle costs
Presently, rising housing costs are a potential brake on the Australian economy and have particular social impacts relating to lower income households. In addition, improved environmental performance of housing is required to avoid undesirable future impacts on the environment and economy of AustraliaHorne, R, Morrissey, J, O’Leary, T, Berry, M, Hamnett, S, Kellett, J, Irvine,
Activation volumes for peroxodisulfate oxidation of cobalt(iii), iron(ii) and nickel(ii) complexes
Dependences of rate constants on pressure (in aqueous solution up to 1.25 kbar) are reported for peroxodisulphate oxidation of hexacyanoferrate(TI), tris(2,2'-bipyridyl)iron(II), tris(l,10-phenanthroline)iron(II), bis(l,4,7-triazacyclononane)nickel(II) and bis(l,2-ethanediamine)cysteinatocobalt(III) and its thioglycollato-analogue, and for periodate oxidation of the two last-named complexes. Derived activation volumes are reported and discussed in terms of intrinsic and solvational contributions. Rate laws and pressure effects on reactivity are reported for the reaction of peroxodisulphate with pentacyanoferrates(II) containing N-alkylpyrazinium ligands.PT: J; CR: ALSHEHRI S, 1992, THESIS LEICESTER ALSHEHRI S, 1993, TRANSIT METAL CHEM, V18, P228 ASANO T, 1978, CHEM REV, V78, P407 BLUNDELL NJ, 1989, INORG CHIM ACTA, V155, P165 BURGESS J, UNPUB BURGESS J, 1966, J CHEM SOC A, P1772 BURGESS J, 1970, J CHEM SOC A, P2114 BURGESS J, 1980, J CHEM SOC CHEM COMM, P350 BURGESS J, 1982, INORG CHIM ACTA, V64, L71 BURGESS J, 1987, TRANSIT METAL CHEM, V12, P238 BURGESS J, 1992, PROGR REACT KINET, V17, P1 HAINES RI, 1981, COORDIN CHEM REV, V39, P77 HALLINAN N, 1987, J ORGANOMET CHEM, V333, P77 HERTING DL, 1978, INORG CHEM, V17, P1649 HOUSE DA, 1962, CHEM REV, V62, P185 IRVINE DH, 1958, J CHEM SOC, P2166 IRVINE DH, 1959, J CHEM SOC, P2977 MCAULEY A, 1984, INORG CHEM, V23, P1938 MILLERO FJ, 1971, CHEM REV, V71, P147 SLOAN CP, 1975, INORG CHEM, V14, P1481 TOMA HE, 1973, INORG CHEM, V12, P1039 VOLLAROVA O, 1983, J CHEM SOC DA, P2359 VOLLAROVA O, 1986, COLLECT CZECH CHEM C, V51, P1049 YEH A, 1985, J AM CHEM SOC, V107, P369; NR: 24; TC: 7; J9: TRANSIT METAL CHEM; PG: 4; GA: MK339Source type: Electronic(1
DNA fusion gene vaccination mobilizes effective anti-leukemic cytotoxic T lymphocytes from a tolerized repertoire
The majority of known human tumor-associated antigens derive from non-mutated self proteins. T cell tolerance, essential to prevent autoimmunity, must therefore be cautiously circumvented to generate cytotoxic T cell responses against these targets. Our strategy uses DNA fusion vaccines to activate high levels of peptide-specific CTL. Key foreign sequences from tetanus toxin activate tolerance-breaking CD4+ T cell help. Candidate MHC class Ibinding tumor peptide sequences are fused to the C terminus for optimal processing and presentation. To model performance against a leukemia-associated antigen in a tolerized setting, we constructed a fusion vaccine encoding an immunodominant CTL epitopederived from Friend murine leukemia virus gag protein (FMuLVgag) and vaccinated tolerant FMuLVgag-transgenic (gag-Tg) mice. Vaccination with the construct induced epitopespecificIFN-c-producing CD8+ T cells in normal and gag-Tg mice. The frequency and avidity of activated cells were reduced in gag-Tg mice, and no autoimmune injury resulted. However, these CD8+ T cells did exhibit gag-specific cytotoxicity in vitro and in vivo. Also, epitope-specific CTL killed FBL-3 leukemia cells expressing endogenous FMuLVgag antigen and protected against leukemia challenge in vivo. These results demonstrate a simple strategy to engage anti-microbial T cell help to activate epitope-specific polyclonal CD8+ T cell responses from a residual tolerized repertoire
J. T. Wiswall papers, W.0011
Abstract: Two notebooks, containing mathematical equations and scientific essays, as well as the handwritten manuscripts of J. T. Wiswall's works "The African" and "Iliad of the Family," neither of which were ever published.Scope and Content Note: The collection contains two small, leather notebooks. One contains the handwritten manuscript "The African" and includes a bookplate identifying Caldwell Delaney as the owner. The other contains the handwritten manuscript "Iliad of the Family," as well as mathematical equations and scientific essays.Biographical/Historical Note: A Mobile, Alabama, author, J. T. Wiswall published two books,
The Last Crusader in 1861 and
Mr. Christopher Katydid (of Casconia) in 1864 (under the pseudonym Mark Heywood). The two handwritten manuscripts in this collection, "The African" and "Iliad of the Family," were never published, although they were listed in Robert E. Bell's
Bibliography of Mobile, which noted that Mobile historian Caldwell Delaney held the manuscripts in his private collection
Letter from J. R. Eakin to Carl Hayden
Letter from J. R. Eakin to Carl T. Hayden concerning access to Rowe Well and the canyon
Letter from J. R. Eakin to Stephen Mather
Letter from J. R. Eakin to Stephen T. Mather about expenses and reconstruction of the Kaibab Trail
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