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1.
Torbjørn Vrålstad Martin Fossen Johan Sjöblom Preben Randhol 《Journal of Dispersion Science and Technology》2013,34(3):440-446
Clay particles with adsorbed asphaltenes, which are commonly found in produced water, have been used as seed particles during precipitation of calcium carbonate in order to determine whether such particles may influence the kinetics of precipitation. The results show that the presence of the adsorbed asphaltenes accelerates the precipitation, and there is also a significant difference between different types of adsorbed asphaltenes. The adsorption of asphaltenes at the seed surface leads to a significant increase in the interfacial tension between the seed surface and the aqueous solution, and calcium carbonate therefore precipitates at the seed surface in order to reduce this high interfacial tension. 相似文献
2.
Jesper L. Mortensen Alan McWilliam Christopher G. Leburn Peter Tidemand-Lichtenberg Morten Thorhauge Jirí Janousek Christian T.A. Brown Alexander A. Lagatsky Preben Buchhave Wilson Sibbett 《Optics Communications》2006,260(2):637-640
Efficient generation of continuous-wave (CW) tunable light in the yellow region is reported. The method is based on sum-frequency mixing of a tunable Cr4+:forsterite laser with a Nd:YVO4 laser. A periodically poled lithium niobate crystal was placed intra-cavity in a Nd:YVO4 laser, and the Cr4+:forsterite laser was single-passed through the non-linear media. With this setup, it was possible to generate up to 3 mW of yellow light smoothly tunable from 573 to 587 nm. This is the highest output demonstrated to date for a tunable diode pumped solid-state CW laser in this wavelength region. The ways to improve the efficiency further are discussed. 相似文献
3.
Preben Dahl Vestergaard 《Graphs and Combinatorics》1991,7(2):197-204
The graphs whose spanning unicyclic subgraphs partition into exactly two isomorphism classes are characterized.This work is a continuation of [6] where graphs with one isomorphism class of spanning unicyclic graphs are characterized. The analogous question for spanning trees was posed in [10] and graphs with one isomorphism class of spanning trees were characterized in [2], [3], [4], [7], [11] while graphs with two isomorphism classes of spanning trees were characterized in [4], [5]. Related topics are treated in [1], [8], [9]. 相似文献
4.
Photolysis of 2,2-dimethyl-1,3-cyclopentanedione in acetone resulted in oxetane formation in a two photon process involving energy transfer from triplet excited acetone and electron transfer from singlet excited acetone. 相似文献
5.
Tønder JE Olesen PH Hansen JB Begtrup M Pettersson I 《Journal of computer-aided molecular design》2001,15(3):247-258
A study of a series of compounds with agonistic effect at the alpha4beta2 nicotinic acetylcholine receptors resulted in an improved pharmacophore model as well as a CoMFA model. The pharmacophore was composed of three pharmacophoric elements: (1) a site point (a) corresponding to a protonated nitrogen atom, (2) a site point (b) corresponding to an electronegative atom capable of forming a hydrogen bond, and (3) the centre of a heteroaromatic ring or a C=O bond (c). The pharmacophoric elements were related by the following parameters: (a-b) 7.3-8.0 A, (a-c) 6.5-7.4 A, and the angle between the two distance vectors (delta bac) 30.4-35.8 degrees. In addition to this, a stereoselective CoMFA model was developed, which showed good predictability even for compound classes not present in the training set. 相似文献
6.
Preben C. Mrk John Ugelstad Jan Ole Aasen 《Journal of polymer science. Part A, Polymer chemistry》1995,33(11):1759-1765
Expressions for calculating the stationary state distribution of radicals in compartmentalized systems with a constant number of reaction loci containing an oil-soluble initiator are given. Besides pairwise formation of radicals in the particles, desorption and reabsorption, water phase termination, solubility of the initiator in the aqueous phase, and the possibility of formation of a single radical species are taken into consideration. The calculation is based on a probabilistic analysis leading to a third-order recurrence relation solved using confluent, hypergeometric Kummer functions. Some calculated curves illustrating the de-pendence of the average number of radicals per particle on various relevant parameters are included. © 1995 John Wiley & Sons, Inc. 相似文献
7.
Boltalina OV Streletskii AV Ioffe IN Hvelplund P Liu B Nielsen SB Tomita S 《The Journal of chemical physics》2005,122(2):021102
The first experimental observation of long-lived triply charged fluorofullerene anions in the gas phase obtained from C60F48 is reported. The existence of a Coloumb barrier trapping the third electron in the trianion is supposed to be responsible for detection of the species which is estimated to have negative third electron affinity. 相似文献
8.
Zhang H Zhang L Tidemand-Lichtenberg P Buchhave P Xu X Li Y 《Photochemistry and photobiology》2011,87(1):131-136
An enzyme (Phospholipase C Type I from Clostridium perfringens) was exposed to 0-810Jcm(-2) of energy using laser light at wavelengths 808, 532, 1064 and 1342nm and two LED light sources at wavelengths 810 and 640nm. Enzyme responses were evaluated by measuring ceramide concentration using high performance thin-layer chromatography (HPTLC) at 0.5, 1, 2, 3, 4, 6, 17, 24h after irradiation. The duration of effect was evaluated from the experimental data. The results show that enzyme activity can be increased by using both laser and LED sources whose wavelength is located within a certain range. The effect depends on the energy and wavelength of the light. The increase in enzyme activity continued for about 4h after irradiation. This study shows that the duration of irradiation should be included as one of the main laser parameters when reporting on the effects of laser irradiation on enzymes. We also find that laser sources and LED sources have the same effect on enzyme activity if the wavelength and absorbed energy are equal. 相似文献
9.
Chakraborty T Holm AI Hvelplund P Nielsen SB Poully JC Worm ES Williams ER 《Journal of the American Society for Mass Spectrometry》2006,17(12):1675-1680
Electron capture by both bare and microsolvated small peptide dications was investigated by colliding these ions with sodium vapor in an accelerator mass spectrometer to provide insight into processes that occur on the microsecond time frame. Survival of the intact peptide monocation after electron capture depends strongly on molecular size. For dipeptides, no intact reduced species were observed; the predominant ions correspond to loss of hydrogen and ammonia. In contrast, the intact reduced species was observed for larger peptides. Calculated structures indicate that the diprotonated dipeptide ions form largely extended structures with low probability of internal ionic hydrogen bonding (i.e., charge solvation) whereas internal ionic H-bonding occurs extensively for larger peptide dications. Solvation of the peptide ions with between one to seven methanol molecules reduces the total extent of H loss even for dipeptides where intact reduced species can survive more than a microsecond after electron capture. The yield of ions corresponding to cleavage of NCalpha bonds (c+ and z+* ions) does not depend strongly on peptide size but decreases with the extent of microsolvation for the dipeptide dications. H-bonding appears to play an important role for the survival of the intact reduced ions but less so for the formation of c+ and z+* ions. Our results indicate that electron capture predominantly occurs at the ammonium groups (at least 70 to 80%), and provides important new insights into the electron capture dissociation process. 相似文献
10.
Moss CL Chung TW Wyer JA Nielsen SB Hvelplund P Tureček F 《Journal of the American Society for Mass Spectrometry》2011,22(4):731-751
Electron transfer and capture mass spectra of a series of doubly charged ions that were phosphorylated pentapeptides of a
tryptic type (pS,A,A,A,R) showed conspicuous differences in dissociations of charge-reduced ions. Electron transfer from both
gaseous cesium atoms at 100 keV kinetic energies and fluoranthene anion radicals in an ion trap resulted in the loss of a
hydrogen atom, ammonia, and backbone cleavages forming complete series of sequence z ions. Elimination of phosphoric acid was negligible. In contrast, capture of low-energy electrons by doubly charged ions
in a Penning ion trap induced loss of a hydrogen atom followed by elimination of phosphoric acid as the dominant dissociation
channel. Backbone dissociations of charge-reduced ions also occurred but were accompanied by extensive fragmentation of the
primary products. z-Ions that were terminated with a deaminated phosphoserine radical competitively eliminated phosphoric acid and H2PO4 radicals. A mechanism is proposed for this novel dissociation on the basis of a computational analysis of reaction pathways
and transition states. Electronic structure theory calculations in combination with extensive molecular dynamics mapping of
the potential energy surface provided structures for the precursor phosphopeptide dications. Electron attachment produces
a multitude of low lying electronic states in charge-reduced ions that determine their reactivity in backbone dissociations
and H- atom loss. The predominant loss of H atoms in ECD is explained by a distortion of the Rydberg orbital space by the
strong dipolar field of the peptide dication framework. The dipolar field steers the incoming electron to preferentially attach
to the positively charged arginine side chain to form guanidinium radicals and trigger their dissociations. 相似文献