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排序方式: 共有237条查询结果,搜索用时 15 毫秒
1.
The self-organizing map (a neural network) was applied to the spectral pattern recognition of voice quality in 34 subjects: 15 patients operated on because of insufficient glottal closure and 19 subjects not treated for voice disorders. The voice samples, segments of sustained /a/, were perceptually rated by six experts. A self-organized acoustic feature map was first computed from tokens of /a/ and then used for the analysis of the samples. The locations of the samples on the map were determined and the distances from a normal reference were compared with the perceptual ratings. The map locations corresponded to the degree of audible disorder: the samples judged as normal were overlapping or close to the normal reference, whereas the samples judged as dysphonie were located further away from it. The comparison of pre- and postoperative samples of the patients showed that the perceived improvement of voice quality was also detected by the map. 相似文献
2.
The effect of ethanol in aqueous eluent on the chromatographic separation was studied at 298 K. Two sugars, L-rhamnose and D-xylose, were separated by using strong and weak cation-exchangers as a stationary phase. The ionic form of the resins was Na+ or Ca2+. The separations were carried out with sugar feed concentrations up to 35 wt% and with both low (about 1%) and high (about 10%) feed volume to bed volume ratios. The separation of the sugars was improved by adding ethanol into the eluent. The separation was also significantly enhanced when the weak cation-exchangers with the greatest affinity for water were used instead of strong cation-exchangers as a separation medium for the sugars having different hydrophilicities. The experimental data were successfully explained with a rate-based column model, which accounted for the volume changes of the stationary phase. A thermodynamic sorption model was utilized in column calculations. 相似文献
3.
The enolate anion of chlorophyll b (Chl b) has been synthesized under deoxygenated conditions and its electronic structure characterized for the first time by 1H NMR and electronic absorption spectroscopy. The formation of the enolate anion caused a marked perturbation to the 18 π-electron [18]diazaannulene aromatic pathway of Chl b. This perturbation appeared as noticeable upfield shifts, exceeding 1 ppm, for the meso-CH protons of the Chl b enolate anion. Nevertheless, the enolate anion remained diatropic, maintaining aromaticity in its delocalized macrocycle. 相似文献
4.
The effect of pH on the formation and stability of phospholipid coatings in fused-silica capillaries in electrophoresis was investigated. A liposome solution consisting of 3 mM of 80:20 mol% phosphatidylcholine/phosphatidylserine (PC/PS) in N-(2-hydroxyethyl)piperazine-N'-(2-ethanesulfonic acid) (HEPES) buffer was used as coating material. The coating was prepared by a method described earlier and five steroids were used as neutral model analytes. First, the effect of pH of the coating solution on the formation and stability of phospholipid coatings was studied at pH 6.5-8.5. The pH of the background electrolyte (BGE) solution (HEPES) was either kept constant at pH 7.4 or made similar to the pH of the liposome coating solution. Results showed that attachment of the coating on the fused-silica wall mostly depends on the protonation of amines of the phospholipids and HEPES. The ability of the phospholipid coating to withstand changes in pH was then investigated by coating at pH 7.5 and separating steroids with acetic acid, 3-(cyclohexylamino)-1-propanesulfonic acid (CAPS), HEPES, or glycine BGE, adjusted to pH between 4.5 and 10.8. The results showed that with use of BGE solution at pH 10.8, the separation of steroids was not successful and the electroosmotic flow was high because of leakage of the phospholipid coating during preconditioning of the capillary with BGE solution. There was no phospholipid leakage with a BGE solution of pH 4.5, indicating that the protonated form of the functional groups of PS and HEPES participating in the attachment of the phospholipid coating to the capillary play an essential role in the success of the coating. 相似文献
5.
The effects of four wash procedures on the concentration of chromium in a pooled sample of human scalp hair are compared. The wash solutions examined are Triton X-100, sodium lauryl sulphate, acetone, and a mixture (1 + 1) of hexane and ethanol. The plateaux reached for hair chromium concentration are functions of the number of washings, and are characteristic for each wash solution. The wash procedure recommended involves two 20-min washes with aqueous 1% sodium lauryl sulphate solution after a hexane rinse. 相似文献
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7.
Pia Willberg-Keyriläinen Jari Vartiainen Ali Harlin Jarmo Ropponen 《Cellulose (London, England)》2017,24(2):505-517
Currently, long-chain cellulose esters are not produced commercially because of high price, and since their preparation typically requires a large quantity of chemicals. To reduce the chemical consumption, cellulose reactivity needs to be increased without losing its quality. One way to increase the reactivity of cellulose is to decrease its molar mass in a controlled manner. In this study, we have synthesized cellulose esters with different side-chain length (C6–C18) in a homogeneous system using ozone molar mass-controlled cellulose. The target was to keep the degree of substitution as low as possible while still ensuring the suitability of cellulose esters for solvent casting. Thermal, barrier and mechanical properties were studied depending on cellulose fatty acid ester side-chain length. All our molar mass-controlled cellulose esters form optically transparent, flexible and heat-sealable films with good water barrier properties and are processable without the addition of an external plasticizer. Furthermore, the films have mechanical properties comparable to some generally used plastics. These good properties suggest that our molar mass-controlled cellulose esters could be potential candidates for various applications such as films and composites. 相似文献
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9.
Konu J Chivers T Tuononen HM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(43):12977-12987
The lithium salts of the chalcogenocarbonyl dianions [(E)C(PPh2S)2]2? (E=S ( 4 b ), Se ( 4 c )) were produced through the reactions between Li2[C(PPh2S)2] and elemental chalcogens in the presence of tetramethylethylenediamine (TMEDA). The solid‐state structure of {[Li(TMEDA)]2[(Se)C(PPh2S)2]}—[{Li(TMEDA)}2 4 c ]—was shown to be bicyclic with the Li+ cations bis‐S,Se‐chelated by the dianionic ligand. One‐electron oxidation of the dianions 4 b and 4 c with iodine afforded the diamagnetic complexes {[Li(TMEDA)]2[(SPh2P)2CEEC(PPh2S)2]} ([Li(TMEDA)]2 7 b (E=S), [Li(TMEDA)]2 7 c (E=Se)), which are formally dimers of the radical anions [(E)C(PPh2S)2]? . (E=S ( 5 b ), Se ( 5 c )) with elongated central E? E bonds. Two‐electron oxidation of the selenium‐containing dianion 4 c with I2 yielded the LiI adduct of a neutral selone {[Li(TMEDA)][I(Se)C(PPh2S)2]}—[{LiI(TMEDA)} 6 c ]—whereas the analogous reaction with 4 b resulted in the formation of 7 b followed by protonation to give {[Li(TMEDA)][(SPh2P)2CSS(H)C(PPh2S)2]}—[Li(TMEDA)] 8 b . Attempts to identify the transient radicals 5 b and 5 c by EPR spectroscopy in conjunction with DFT calculations of the electronic structures of these paramagnetic species and their dimers are also described. The crystal structures of [{Li(TMEDA)}2 4 c ], [{LiI(TMEDA)} 6 c ] ? C7H8, [Li(TMEDA)]2 7 b? (CH2Cl2)0.33, [Li(THF)2]2 7 b , [Li(TMEDA)]2 7 c , [Li(TMEDA)] 8 b? (CH2Cl2)2 and [Li([12]crown‐4)2] 8 b were determined and salient structural features are discussed. 相似文献
10.
Nieminen JO Vesanen PT Zevenhoven KC Dabek J Hassel J Luomahaara J Penttilä JS Ilmoniemi RJ 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2011,212(1):154-160
In ultra-low-field magnetic resonance imaging (ULF MRI), superconductive sensors are used to detect MRI signals typically in fields on the order of 10-100 μT. Despite the highly sensitive detectors, it is necessary to prepolarize the sample in a stronger magnetic field on the order of 10-100 mT, which has to be switched off rapidly in a few milliseconds before signal acquisition. In addition, external magnetic interference is commonly reduced by situating the ULF-MRI system inside a magnetically shielded room (MSR). With typical dipolar polarizing coil designs, the stray field induces strong eddy currents in the conductive layers of the MSR. These eddy currents cause significant secondary magnetic fields that may distort the spin dynamics of the sample, exceed the dynamic range of the sensors, and prevent simultaneous magnetoencephalography and MRI acquisitions. In this paper, we describe a method to design self-shielded polarizing coils for ULF MRI. The experimental results show that with a simple self-shielded polarizing coil, the magnetic fields caused by the eddy currents are largely reduced. With the presented shielding technique, ULF-MRI devices can utilize stronger and spatially broader polarizing fields than achievable with unshielded polarizing coils. 相似文献