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Kaishuo Yang Ehsan Sadeghi Pouya Libin Liu Dr. Ming Li Dr. Xiaoxian Yang Dr. Neil Robinson Prof. Eric F. May Prof. Michael L. Johns 《Chemphyschem》2022,23(4):e202100794
Understanding the behaviour of short-chain hydrocarbons confined to porous solids informs the targeted extraction of natural resources from geological features, and underpins rational developments in separation, storage and catalytic conversion processes. Herein, we report the application of low-field (12.7 MHz) 1H nuclear magnetic resonance (NMR) relaxation measurements to characterise ethane dynamics within mesoporous silica materials exhibiting mean pore diameters between 6 and 50 nm. Our measurements provide NMR-based adsorption isotherms within the range 25–50 bar and at ambient temperature, incorporating the ethane condensation point (40.7 bar at our experimental temperature of 23.6 °C). The quantitative nature of the acquired data is validated via a direct comparison of NMR-derived excess adsorption capacities with ex situ gravimetric ethane adsorption measurements, which are demonstrated to agree to within 0.2 mmol g−1 of the observed ethane capacity. NMR relaxation time distributions are further demonstrated as a means to decouple interparticle and mesopore dominated adsorption phenomena, with unexpectedly rapid relaxation rates associated with interparticle ethane gas confirmed via a direct comparison with NMR self-diffusion analysis. 相似文献
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Abstract— The phototactic response of Euglena gracilis is suppressed when the organisms are exposed to bright light of wavelength less than 650 nm. Activity returns in the dark, approximately 40 min being required for full restoration. Action spectral measurements demonstrate that the receptor pigment which mediates the suppression response may be a flavoprotein. Evidence is presented which indicates that photosuppression involves a direct action on the photo-tactic apparatus, perhaps a photobleaching of the tactic photoreceptor pigment. 相似文献
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Nielsen RD Che K Gelb MH Robinson BH 《Journal of the American Chemical Society》2005,127(17):6430-6442
Both the oxygen diffusion rate and the oxygen solubility vary with depth into the interior of biological membranes. The product of these two gradients generates a single gradient, a permeability gradient, which is a smooth continuous function of the distance from the center of the membrane. Using electron paramagnetic resonance and the spin-probe method, the relaxation gradient of oxygen, which is directly proportional to the permeability gradient, is the quantity that can be directly measured in membranes under physiological conditions. The gradient obtained provides a calibrated ruler for determining the membrane depth of residues either from loop regions of membrane-binding proteins or from the membrane-exposed residues of transmembrane proteins. We have determined the relaxation gradient of oxygen in zwitterionic and anionic phospholipid membranes by attaching a single nitroxide probe to a transmembrane alpha-helical polypeptide at specific residues. The peptide ruler was used to determine the depth of penetration of the calcium-binding loops of the C2 domain of cytosolic phospholipase A(2). The positions of selected residues of this membrane-binding protein that penetrate into the membrane, determined using this ruler, compared favorably with previous determinations using more complex methods. The relaxation gradient constrains the possible values of the membrane-dependent oxygen concentration and the oxygen diffusion gradients. The average oxygen diffusion coefficient is estimated to be at least 2-fold smaller in the membrane than that in water. 相似文献
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The concept of an EP matrix is extended to a morphism of a category C with involution. It is shown that an EP morphism has a group inverse iff it has a Moore-Penrose inverse, and in this case the inverses are identical. On the other hand, if a morphism has a Moore-Penrose inverse that is a group inverse, then C is a full subcategory of a category in which φ is EP. Also, if C is an additive category with involution 1 and with 1-biproduct factorization, then a morphism of φ of C is EP iff there is a 1-biproduct J ⊕ K and an invertible morphism θ : J → J such that φ is congruent to a morphism of the form In particular, a square matrix over a principal-ideal domain with involution is EP iff it is congruent to a matrix of the form dg(θ, 0) with θ invertible. 相似文献
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Glow discharge mass spectrometry 总被引:5,自引:0,他引:5
Hoffmann V Kasik M Robinson PK Venzago C 《Analytical and bioanalytical chemistry》2005,381(1):173-188
Over the past twenty years or so, glow discharge mass spectrometry (GDMS) has become the industry standard for the analysis of trace elements in metals and semiconductors. A review of its history is followed by a picture of the present situation and a look to where the future may lie. Applications are summarised, including the ability of GDMS to offer depth-resolved data and non-conductor analysis, and the well-documented quantitative nature of the results is reviewed. The effects resulting from the physical properties of the analyte material are discussed at length. Finally, recent work such as fast flow sources and pulsed glow discharges is reviewed. 相似文献
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A selective gas chromatographic detector for polynuclear aromatics based on ultraviolet fluorescence
A vapor-phase fluorescence detector for the analysis of mixtures of polynuclear aromatic ring systems has been developed. This system utilizes wide bandpass excitation and wide band emission filters, thus increasing sensitivity and decreasing the complexity of previously designed instruments. The sensitivity of the detector has been demonstrated to be at the nanogram level with reasonable precision. 相似文献
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Mathematical consideration of the course of neutralization of a solution containing a moles of a strong base (e.g. sodium hydroxide) and a moles of a salt of a weak dibasic acid (e.g. sodium carbonate) with a strong acid (e.g. hydrochloric acid) shows that the first derivative of the titration curve should contain three maxima. The first, corresponding to neutralization of most of the hydroxide, is small (with height proportional to a), displaced slightly from the equivalence point, and disappears for a less than 0.01 mol l-1. The second corresponds to the conversion of most of the CO32- to HCO3- and its height is almost independent of a. The third corresponds to the conversion of HCO3- to H2CO3, with height proportional to a. The two minima are independent of a and of the dissociation constants of the weak acid. These conclusions were examined experimentally and were extended to the titration of hydroxide contaminated with a small amount of carbonate. 相似文献