The effect of a magnetic tape coating process on the structure and properties of a semi-crystalline polymer

A combination of structure identifying and bulk property experiments were combined with a two-phase analytical methodology to elucidate the influence of a magnetic tape coating process on the substrate polymer film. Employing a typical tape manufacturing process that utilizes coating, drying, and calendering stages, polyethylenete-rephthalate polymer film samples with and without the magnetic coating were prepared.Experiments and modeling studies performed on these samples demonstrate that the drying and calendering processes may increase the crystallinity and noncrystalline orientation of the substrate film. In addition, dynamic mechanical experiments identified a viscoelastic transition at 50 °C for the PET substrate film sample which is near the glass transition of the magnetic coating utilized. Overall, the results of this investigation provide a basis for evaluating structure property interrelations of polymer-based magnetic tapes.     

Synthesis of 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-ones utilizing activated alkynoates

The synthesis of the biologically relevant, 4-trifluoromethylpyrido[1,2-a]pyrimidin-2-one 7, is reported. Addition of substituted 2-aminopyridines 5 to activated alkynoates leads to the facile formation of a series of metabolically stable trifluoromethyl substituted pyrido[1,2-a]pyrimidines under mild conditions.     

Mechanism and kinetics of the reaction of F with trivalent phosphorus iodide using electron spin resonance detection

The reaction of iodobistrifluoromethylphosphine, P(CF₃)₂I, with atomic fluorine was studied by fast-flow ESR methods. The initial stage of the reaction is the abstraction of I by F, to form IF with a bimolecular rate constant of (1.0 ± 0.3) × 10¹⁴ cm³ mol^?1 s^?1 at 297 K. In the presence of excess F, stepwise addition to the phosphorous occurs. In the presence of excess P(CF₃)₂I, the reaction P(CF₃)₂ + IF → P (CF₃)₂F + I appears to take place. This reaction rate is slow relative to P(CF₃)₂ + F → P(CF₃)₂F.     

Measurement of the heavy neutrino admixture upper limit from muon capture by3He

The triton energy spectrum of the muon capture reaction µ³Het+_µ where µ³He is the ground state of muonic³He, has been measured by means of a high-pressure ionization chamber in order to investigate a possible heavyv admixture into the µ flavor with high sensitivity. The upper limit of the µ-heavy v_i mixing matrix element squared was obtained to be U_µi²10^–3 for heavy neutrino masses in the range of 25 E_0V75 MeV.     

Antiflow of K(0)(s) mesons in 6A GeV Au + Au collisions

We have measured the sideward flow of neutral strange ( K(0)(s)) mesons in 6A GeV Au+Au collisions. A prominent antiflow signal is observed for an impact parameter range ( b less, similar7 fm) which spans central and midcentral events. Since the K(0)(s) scattering cross section is relatively small in nuclear matter, this observation suggests that the in-medium kaon vector potential plays an important role in high density nuclear matter.     

Rotating orthogonal polarization imaging

Surface reflections often present a problem in the polarization difference imaging of tissue. The technique described involves illumination in a single polarization state and detection in the orthogonal polarization state. Synchronously rotating both the illumination and orthogonal detection states provides an image free from surface reflections that is sensitive to the polarization properties of the underlying tissue. Results on tissue phantoms demonstrate that polarization sensitive measurements of a test target can be made up to a depth of 12 mean free paths within a scattering medium. Preliminary images of bovine tendon are also demonstrated.     

Alkyl‐Tethered Bis‐Phosphoryl Compounds with two 1,3,2‐Benzodiazaphosphorinone Units; Oxidation,Complexation, and X‐Ray Structure Analysis of Selected Compounds

The reaction of the bis‐chlorophosphines 1 a – 1 d with bis(2‐chloroethyl)amine hydrochloride in the presence of triethylamine and with various trimethylsilylamines led to a new class of bis‐phosphorus ligands 2 a – 2 c and 3 a – 3 g . ³¹P‐NMR studies suggested that the bis‐phosphorus ligands undergo rotation reactions about the alkyl bridge in polar solvents. Compounds 2 a – 2 c showed initially only one sharp singlet each in their ³¹P‐NMR spectra. After a few days at room temperature, two signals were observed. Similar results were observed for 3 a – 3 g . In the solid state, the two phosphorus atoms in 2 c are not equivalent, as was confirmed by the observation of two signals in the solid state ³¹P‐NMR spectrum. Oxidation reactions of 2 a – 2 c by the hydrogen peroxide‐urea 1 : 1 adduct (NH₂)₂C(:O) · H₂O₂ led to the formation of the corresponding phosphoryl compounds 4 a – 4 c . Reaction of 2 a and 3 a with Pt[COD]Cl₂ (COD = 1.5‐Cyclooctadiene) furnished the complexes 5 and 6 . The NMR spectra suggested that the two chlorine atoms are in cis position. X‐ray structure analyses were conducted for 2 a , which exhibits twofold symmetry; 2 c , which is linked into dimers by hydrogen bonds C–H…O; and 6 , confirming the cis configuration.     

Development of a New Experimental Method for Studies of Muon Capture in Hydrogen

A new experiment is under preparation with the aim to improve considerably the present knowledge of the rate Λ _s , which should be measured on a level of 1% or better, for the basic electroweak capture reaction of a negative muon on the free proton μp _1s → n + ν_μ. The capture rate will be determined by measuring the lifetime of μ⁻ stopped in ultra pure hydrogen at 10 bar pressure and comparing it with the lifetime of the unbound μ⁺. A new experimental method was developed for this project which should allow measuring the μ⁻ lifetime with at least 10 ppm precision. The basic element of the detector is operating in the hydrogen gas time projection chamber (TPC) surrounded by multi-wire proportional chambers (MWPCs) and scintillator counters. The arrival times and trajectories of the incoming muons and the outgoing decay electrons are measured with this device providing effective suppression of background. Using the TPC as an active target, we can monitor on-line the protium contamination by impurities with a sensitivity better than 10⁻⁸. This can be done by detecting the charged products of the muon capture reaction on these impurities. It was demonstrated that the TPC and MWPCs can operate in pure hydrogen under 10 bar pressure providing gas gain up to 10 000. This revised version was published online in August 2006 with corrections to the Cover Date.     

Insights on d μ t sticking from d μ d stripping and μ,3He capture

Data from the recent PSI high statistics experiment on d μ d fusion are used to measure the stripping process in d μ d→ n+μ,³He and test current calculations of the stripping process. The PSI results in μ³He capture are also used to remove a troubling background from this measurement. Combination of these results with the old dμ t sticking analysis slightly raise and improve that result to ω_s= (0.58± 0.04)% and indicate that theory and experiment can meet if theoretical stripping is increased only at the beginning of the track. This conclusion is in accord with the new stripping calculations where excited state stripping is increased significantly. This revised version was published online in August 2006 with corrections to the Cover Date.     

A host-guest optical sensor for aliphatic amines based on lipophilic cyclodextrin

A host-guest optical sensor for the determination of aliphatic amines as exemplified by octylamine is proposed. It is based on the reversible fluorescence enhancement of heptakis(2,6-di-O-isobutyl)-β-cyclodextrin(DOB-β-CD) hosting tetraphenylporphyrin (TPP) immobilized in poly(vinyl chloride) (PVC) membrane by aliphatic amine extracted from aqueous phase into membrane phase. The optimum membrane contained 1.15 wt % TPP, 6.15 wt % DOB-β-CD as sensing reagent and other membrane materials. The fluorescence enhancement of the membrane resulted from the formation of a stable three-component complex among DOB-β-CD, TPP, and aliphatic amines. With the optimum conditions described, the fluorescence response of the sensor to octylamine shows a good correlation with the theoretically derived equation in the range 1.0 × 10^–6 to 8.0 × 10^–4 mol/L. The response characteristics including reversibility, response time, reproducibility and lifetime and selectivity of this optical device are also discussed in detail. This sensor has also been applied for the determination of octylamine in water samples containing interferents with satisfactory recovery. Received: 21 November 1999 / Revised: 10 January 2000 / Accepted: 15 January 2000