Fast measurements of average flow velocity by Low-Field ¹H NMR

In this paper, we describe a method for measuring the average flow velocity of a sample by means of Nuclear Magnetic Resonance. This method is based on the Carr-Purcell-Meiboom-Gill (CPMG) sequence and does not require the application of any additional static or pulsed magnetic field gradients to the background magnetic field. The technique is based on analyzing the early-time behavior of the echo amplitudes of the CPMG sequence. Measurements of average flow velocity of water are presented. The experimental results show a linear relationship between the slope/y-intercept ratio of a linear fit of the first echoes in the CPMG sequence, and the average flow velocity of the flowing fluid. The proposed method can be implemented in low-cost Low-Field NMR spectrometers allowing a continuous monitoring of the average velocity of a fluid in almost real-time, even if the flow velocity changes rapidly.     

Laser heating of solid matter by light-pressure-driven shocks at ultrarelativistic intensities

The heating of solid targets irradiated by 5 x 10(20) W cm(-2), 0.8 ps, 1.05 microm wavelength laser light is studied by x-ray spectroscopy of the K-shell emission from thin layers of Ni, Mo, and V. A surface layer is heated to approximately 5 keV with an axial temperature gradient of 0.6 microm scale length. Images of Ni Ly(alpha) show the hot region has 100 G bar light pressure compresses the preformed plasma and drives a shock into the solid, heating a thin layer.     

Influence of speech stimuli intensity on the activation of auditory cortex investigated with functional magnetic resonance imaging.

Understanding the impact of variations in the acoustic signal is critical for the development of auditory and language fMRI as an experimental tool. We describe the dependence of the BOLD signal and speech intelligibility on the intensity of auditory stimuli. Eighteen subjects were imaged on a 1.5-T MRI scanner. Speech stimuli were English monosyllabic words played at five intensity levels. Intrasubject reproducibility was measured on one subject by presenting the stimulus five times at the same intensity level. Intelligibility was measured during data acquisition as subjects signaled when hearing two targets. Each functional trial consisted of four cycles (30 s off-30 s on). Five oblique slices covering primary and association auditory areas were imaged. Activated voxels were identified by cross-correlation analysis and their percent signal change (delta S) was measured. Intersubject differences in activation extent, asymmetry, and dependence on intensity were striking. Volume of activation was significantly greater in the left than in the right hemisphere. Intrasubject reproducibility for delta S was higher than for volume of activation. delta S and intelligibility showed a similar dependence on intensity suggesting that not only intensity but also intelligibility affect the fMRI signal.     

Sorption and transport of hydrocarbon and perfluorocarbon gases in poly(1‐trimethylsilyl‐1‐propyne)

Pure gas solubility and permeability of H₂, O₂, N₂, CO₂, CH₄, C₂H₆, C₃H₈, CF₄, C₂F₆, and C₃F₈ in poly(1‐trimethylsilyl‐1‐propyne) (PTMSP) were determined as a function of pressure at 35°C. Permeability coefficients of the perfluorinated penetrants are approximately an order of magnitude lower than those of their hydrocarbon analogs, and lower even than those of the permanent gases. In striking contrast to hydrocarbon penetrants, PTMSP permeability to fluorocarbon penetrants decreases with increasing penetrant size. This unusual size‐sieving behavior in PTMSP is attributed to low perfluorocarbon solubilities in PTMSP coupled with low diffusion coefficients relative to those of their hydrocarbon analogs. In general, perfluorocarbon penetrants are less soluble than their hydrocarbon analogs in PTMSP. The difference in hydrocarbon and perfluorocarbon solubilities in high free volume, hydrocarbon‐rich PTMSP is much smaller than in hydrocarbon liquids and liquidlike polydimethylsiloxane. The low solubility of perfluorocarbon penetrants is ascribed to the large size of the fluorocarbons, which inhibits their dissolution into the densified regions of the polymer matrix and reduces the number of penetrant molecules that can be accommodated in Langmuir sites. From the permeability and sorption data, diffusion coefficients were calculated as a function of penetrant concentration. With the exception of H₂ and the C₃ analogs, all of the penetrants exhibit a maximum in their concentration‐dependent diffusion coefficients. Resolution of diffusion coefficients into a mobility factor and a thermodynamic factor reveals that it is the interplay between these two terms that causes the maxima. The mobility of the smaller penetrants (H₂, O₂, N₂, CH₄, and CO₂) decreases monotonically with increasing penetrant concentration, suggesting that the net free volume of the polymer–penetrant mixture decreases as additional penetrant is added to PTMSP. For larger penetrants mobility either: (1) remains constant at low concentrations and then decreases at higher penetrant concentrations (C₂H₆, CF₄, and C₂F₆); (2) remains constant for all concentrations examined (C₃H₈); or (3) increases monotonically with increasing penetrant concentration (C₃F₈). Presumably these results reflect the varying effects of these penetrants on the net free volume of the polymer–penetrant system. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 273–296, 2000     

Long-term permeation properties of poly(1-trimethylsilyl-1-propyne) membranes in hydrocarbon—Vapor environment

Poly(1-trimethylsilyl-1-propyne) (PTMSP), a high free-volume glassy di-substituted polyacetylene, has the highest gas permeabilities of all known polymers. The high gas permeabilities in PTMSP result from its very high excess free volume and connectivity of free volume elements. Permeability coefficients of permanent gases in PTMSP decrease dramatically over time due to loss of excess free volume. The effects of aging on gas permeability and selectivity of PTMSP membranes continuously exposed to a 2 mol % n-butane/98 mol % hydrogen mixture over a period of 47 days are reported. The permeation properties of PTMSP membranes are quite stable when the polymer is continuously exposed to a gas mixture containing a highly sorbing organic vapor such af n-butane. The n-butane/hydrogen selectivity was essentially constant for the 47-day test period at a value of 29, or 88% of the initial value of the as-cast film of 33. Condensable gases such as n-butane may serve as a “filler” in the nonequilibrium free volume of the polymer, thereby preserving the high level of excess free volume. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35 : 1483–1490, 1997     

Augmenting the Performance of Hydrogenase for Aerobic Photocatalytic Hydrogen Evolution via Solvent Tuning

This work showcases the performance of [NiFeSe] hydrogenase from Desulfomicrobium baculatum for solar-driven hydrogen generation in a variety of organic-based deep eutectic solvents. Despite its well-known sensitivity towards air and organic solvents, the hydrogenase shows remarkable performance under an aerobic atmosphere in these solvents when paired with a TiO₂ photocatalyst. Tuning the water content further increases hydrogen evolution activity to a TOF of 60±3 s⁻¹ and quantum yield to 2.3±0.4 % under aerobic conditions, compared to a TOF of 4 s⁻¹ in a purely aqueous solvent. Contrary to common belief, this work therefore demonstrates that placing natural hydrogenases into non-natural environments can enhance their intrinsic activity beyond their natural performance, paving the way for full water splitting using hydrogenases.     

Approaching Dianionic Tetraoxadiborecine Macrocycles: 10-Membered Bora-Crown Ethers Incorporating Borafluorenate Units

The addition of non-benzenoid quinones, acenapthenequinone or aceanthrenequinone, to the 9-carbene-9-borafluorene monoanion ( 1 ) affords the first examples of dianionic 10-membered bora-crown ethers ( 2 – 5 ), which are characterized by multi-nuclear NMR spectroscopy (¹H, ¹³C, ¹¹B), X-ray crystallography, elemental analysis, and UV/Vis spectroscopy. These tetraoxadiborecines have distinct absorption profiles based on the positioning of the alkali metal cations. When compound 4 , which has a vacant C₄B₂O₄ cavity, is reacted with sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, a color change from purple to orange serves as a visual indicator of metal binding to the central ring, whereby the Na⁺ ion coordinates to four oxygen atoms. A detailed theoretical analysis of the calculated reaction energetics is provided to gain insight into the reaction mechanism for the formation of 2 – 5 . These data, and the electronic structures of proposed intermediates, indicate that the reaction proceeds via a boron enolate intermediate.