Search results for "mass distribution"
showing 10 items of 290 documents
One-pot synthesis and characterization of aliphatic poly(oxytetramethylene) ionene
2002
Abstract One-pot synthesis of poly(oxytetramethylene) ionene (POI) composed of one dimethylammonium group in each repeating unit is described. POI was prepared by using the cationic polymerization of tetrahydrofuran, followed by the chain extension reaction of living poly(oxytetramethylene) (POTM) chain with N , N -dimethylaminotrimethylsilane. The weight average molecular weight of the ionene with bromide counter-anion (POI–Br) was 48,000 g/mol and the molecular weight of POTM between the ionic sites was ca. 2100. POI–Br showed polyelectrolyte behavior in polar solvent. The elastomeric film of POI–Br was prepared: its tensile strength at break and elongation at break were ca. 11 MPa and ca…
Spatial Distribution and Abundance of Mesopelagic Fish Biomass in the Mediterranean Sea
2020
Mesopelagic fish, being in the middle of the trophic web, are important key species for the marine environment; yet limited knowledge exists about their biology and abundance. This is particularly true in the Mediterranean Sea where no regional assessment is currently undertaken regarding their biomass and/or distribution. This study evaluates spatial and temporal patterns of mesopelagic fish biomass in the 1994–2011 period. We do that for the whole Mediterranean Sea using two well-established statistical models, the Generalized Additive Model (GAM) and Random Forest (RF). Results indicate that the bathymetry played an important role in the estimation of mesopelagic fish biomass and in its …
Size-Exclusion Chromatographic Determination of Polymer Molar Mass Averages Using a Fractal Calibration
2005
The characterization of polymers by size-exclusion chromatography basically consists of the determination of the weight-average molar mass (Mw), number-average molar mass (Mn), and polydispersity index (I). An accurate estimation of these magnitudes requires the use of a reliable and trusted calibration curve. Three procedures for building up a calibration curve are analyzed in this work. The first is the classical universal calibration (UC), based on the elution of tetrahydrofuran-polystyrene in a system as reference. The second is based on the proper calibration curve made with standards of the sample under study. However, two main drawbacks arise when using these methodologies: the nonfu…
Apparent Molar Mass of a Polyelectrolyte in an Organic Solvent in the Low Ionic Strength Limit As Revealed by Light Scattering
2013
The apparent molar mass of a partially quaternized poly-2-vinylpyridines (degree of quaternization 4.3% < Q < 35%) in 1-propanol is measured by light scattering at low ionic strength (10–6 M < cs < 10–3 M) as a function of polyion repeat unit concentration (7 × 10–5 monomol/L < cm,p < 4 × 10–2 monomol/L). No dialysis was applied prior to measurements. The apparent molar mass under “salt-free” conditions is smaller than the true molar mass by an order of magnitude, while approaching the true value at higher ionic strength. Concomitant data on the dependence of scattering intensity on scattering wave vector show that the dilute polyelectrolyte solutions are strongly correlated. A recent theor…
Characterization of lignin dissolved during alkaline pretreatment of softwood and hardwood
2015
Various alkaline pretreatments were applied to Scots pine (Pinus sylvestris) and silver/white birch (Betula pendula/pubescens) wood chips and the characterization of sulfur-free lignin dissolved was performed. The behavior of lignin during these pretreatments (alkali charge 1–8% NaOH, time 30–120 minutes, and temperature 130–150°C) was studied mainly in terms of lignin removal efficiency and molar mass distribution of dissolved lignin. The amount of lignin in pretreatment liquors increased along with an increase in the alkali charge of 0.8–4.4% and 0.6–3.4% of o.d. pine and birch wood, respectively. The most significant parameter affecting the molar mass of the dissolved lignin was shown to…
1971
The polymerisation of ethylene was carried out in the presence of (C5H5)2TiCl2/(C2H5)2AlCl in benzene (I) and of TiCl4/(C2H5)AlCl2 in chlorobenzene (II). In the initial state of the polymerisation with I oligomers with a narrow molecular weight distribution are formed. According to their IR and NMR spectra they were identified as predominantly saturated linear hydrocarbons. The effect of a substitution of the cyclopentadienyl rings by R = CH3 and C2H5 was studied as well as the influence of aging particularly on the molecular weight distribution. The catalytic system II yields predominantly unsaturated branched oligomers with broad molecular weight distribution. The ligand effect on the str…
Effects of shadowing on Drell-Yan dilepton production in high energy nuclear collisions
2001
We compute cross sections for the Drell-Yan process in nuclear collisions at next-to-leading order (NLO) in ��_s. The effects of shadowing on the normalization and on the mass and rapidity dependence of these cross sections are presented. An estimate of higher order corrections is obtained from next-to-next-to-leading order (NNLO) calculation of the rapidity-integrated mass distribution. Variations in these predictions resulting from choices of parton distribution sets are discussed. Numerical results for mass distributions at NLO are presented for RHIC and LHC energies, using appropriate rapidity intervals. The shadowing factors in the dilepton mass range 2 < M < 10 GeV are predicted…
Fragment mass distribution in superasymmetric region in proton-induced fission of U and Th
1998
Fission fragment mass distributions down to super-asymmetric mass region and both pre- and post-scission neutron multiplicity for238U(p,fission) reaction atEp = 20, 35, 50, 60 MeV and for232Th(p, fission) reaction atEp = 50, 60 MeV were measured using HENDES set-up. The results indicate enhancement for super-asymmetric mass division at intermediate excitation energies.
Hypernuclear spectroscopy of products from Li-6 projectiles on a carbon target at 2 A GeV
2013
WOS: 000322848900009
Study of e+e−→γωJ/ψ and Observation of X(3872)→ωJ/ψ
2019
We study the e^{+}e^{-}→γωJ/ψ process using 11.6 fb^{-1} e^{+}e^{-} annihilation data taken at center-of-mass energies from sqrt[s]=4.008 GeV to 4.600 GeV with the BESIII detector at the BEPCII storage ring. The X(3872) resonance is observed for the first time in the ωJ/ψ system with a significance of more than 5σ. The relative decay ratio of X(3872)→ωJ/ψ and π^{+}π^{-}J/ψ is measured to be R=1.6_{-0.3}^{+0.4}±0.2, where the first uncertainty is statistical and the second systematic (the same hereafter). The sqrt[s]-dependent cross section of e^{+}e^{-}→γX(3872) is also measured and investigated, and it can be described by a single Breit-Wigner resonance, referred to as the Y(4200), with …