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Process yields difunctional isobutylene polymers ranging in molecular weight from 1150 to 3600. These polymers have the potential for copolymerization and cross-linking with other monomers to form elastomeric materials.
Results from the first flight of our proportional counter in an imaging telescope led us to rebuild the detector. We have used a Penning gas mixture (xenon + 1 percent isobutylene) and introduced a preamplification region to improve the energy resolution. We have rebuilt the pressure vessel making novel use of molybdenum as the housing material in order to reduce the residual instrument background, particularly in the fluorescence-gated mode for which the detector design has been optimized. We have also increased the sensitive gas depth from 9 to 14 cm to further increase the sensitivity to both fluorescent pairs and conventional singles. Our calibrations have shown that the overall energy resolution of the detector has been enhanced by a factor of 2, and we predict that the sensitivity at float will increase by a factor of 3 in the 50-70 keV energy band.
The second generation of the Marshall Imaging X-ray Experiment (MIXE2) was flown from Fort Sumner, New Mexico on May 7-8, 1997. The experiment consists of coded-aperture telescope with a field of view of 1.8 degrees (FWHM) and an angular resolution of 6.9 arcminutes. The detector is a large (7.84x10(exp 4) sq cm) effective area microstrip proportional counter filled with 2.0x10(exp5) Pascals of xenon with 2% isobutylene. We present MIXE2 observation of the 20-80keV spectrum and timing variability of Cygnus X-1 made during balloon flight.
Conformational energy contours of perfluoroalkanes, determined from ab initio calculations, confirm the well-known spitting of trans states into two minima at plus or minus 17 degrees but also show that the gauche states split as well, with minima at plus or minus 124 degrees and plus or minus 84 in order to relieve steric crowding. The directions of such split distortions from the perfectly staggered states are strongly coupled for adjacent pairs of bonds in a manner identical to the intradyad pair for poly (isobutylene) chains. These conformational characteristics are fully represented by a six-state rotational isomeric state (RIS) model for PTFE comprised of t(+), t(-), g(sup +)+, g(sup +)-, g(sup -) + and g(sup -)-states, located at the split energy minima. The resultant 6 x 6 statistical weight matrix is described by first-order interaction parameters for the g+(+) (ca. 0.6 kcal/mol) and g+- (ca. 2.0 kcal/mol) states, and second order parameters for the g(sup +)+g(sup +)+ (ca 0.6 kcal/mol) and g(sup +)+g(sup -)+ (ca. 1.0 kcal/mol) states. This six-state RIS model, without adjustment of the geometric or energy parameters as determined from the ab initio calculations, predicts the unperturbed chain dimensions and the fraction of gauche bonds as a function of temperature for PTFE in good agreement with available experimental values.
Disclosed is a catalyst system, its methods of preparation and its use for producing, among others, alkenes and/or saturated or unsaturated oxygenates and, which include at least one of an aldehyde and an acid (such as propyl aldehyde, acrolein, acrylic acid, isobutyl aldehyde, methacrolein, methacrylic acid), comprising subjecting the corresponding an alcohol or a diol selected from the group consisting of propanol, propanediol and isobutanol that is derivable from biomass, to a vapor phase process over the catalytic system described herein in the presence of a gas mixture of oxygen, air or nitrogen and/or other suitable diluting gas. In the case where one of 1-propanol, or 1,2-propanediol or 1,3-propanediol or a mixture thereof is subjected to a vapor phase catalytic process over the said catalytic system in the presence of air or oxygen, and a co-fed gas, such as nitrogen or other diluting gas, the product is at least one of propylene, propyl aldehyde, acrolein and acrylic acid. In the case where isobutanol is subjected to such a process, the product is at least one of isobutylene, isobutyl aldehyde, methacrolein and methacrylic acid. The catalyst system comprises a single catalytic zone or multi-catalytic zones, in each of which the composition of the co-feed and other reaction parameter can be independently controlled.
TinyTPC, a compact LArTPC with a pixelated readout system (LArPix), aims to improve energy measurements for low-energy events by enhancing ionization charge collection. It explores the effects of photosensitive dopants and xenon in liquid argon. An initial look at adding photosensitive dopant isobutylene found a 5% charge enhancement.
TinyTPC is a small scale liquid-argon time projection chamber (LArTPC) that studies how photosensitive dopants can improve the energy resolution of low energy events in LArTPCs. Bench tests to resolve high voltage breakdown issues and to improve the low voltage system readout are described. Experimental data with a radioactive source of Th-228 for the calibration of the pixelated readout and the characterization of TinyTPC's energy resolution is explained. Provisional results from the addition of isobutylene (photosensitive dopant) and xenon (wavelength shifter) to liquid-argon (LAr) are also presented. Further steps to improve voltage system and enhance the data collection are discussed.
Pressure drop as function of flow rate for helical flow of non-Newtonian polyisobutylene solution