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21.
This paper investigates the use of NiO particles to enhance the vapour sensing properties of polyethylene adipate (PEA)\carbon black (CB) composite materials. Four PEA\CB suspensions were prepared with 0, 10, 20 and 30 w/w% NiO, respectively. Hypermer PS3 surfactant was shear mixed into each of the suspensions for 300 s to achieve a homogenous dispersion and to prevent reagglommeration of both the CB and NiO particles. A 0.1 μl drop of each composite was deposited between Cu electrodes on a printed circuit board (PCB) substrate using a microlitre syringe. The samples were allowed to dry for 24 h in an oven at 333 K to remove any remaining solvent. After preparation, the sensors were exposed to propanol and butanol at concentrations ranging from 0 to 25 000 ppm in steps of 5000 ppm. The response of the PEA\CB sensors improved significantly as the concentration of NiO particles in the material increased and maximum relative differential responses as high as 37% and 92.8% were recorded after exposure to 25 000 ppm propanol and butanol, respectively. This high response can be explained using the Flory–Huggins interaction parameter along with structural changes in the polymer composite caused by the addition of NiO. This paper concludes that NiO particles can be used as a method to increase the sensitivity of existing conducting polymer composite gas sensing materials.  相似文献   
22.
The essential oil composition of Satureja thymbra was analyzed by direct thermal desorber and Headspace GC/MS analysis methods. Its constituents were determined to be mainly carvacrol (40.15%), gamma-terpinene (26.56%), p-cymene (16.39%), and thymol (13.16%). The other techniques, thermal desorber and Headspace GC/MS, were used for the plant leaves at three different temperature, which showed similar results. The thermal desorber GC/MS gave better and more sensitive results than Headspace GC/MS. The essential oil was found to be active against the bacteria Escherichia coli, Pseudomonas aeruginosa, Salmonella typhimurium, Shigella sonnei, and Staphylococcus aureus and the yeast Candida albicans.  相似文献   
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Background  

The hippocampus is essential for declarative memory synthesis and is a core pathological substrate for Alzheimer's disease (AD), the most common aging-related dementing disease. Acute increases in plasma cortisol are associated with transient hippocampal inhibition and retrograde amnesia, while chronic cortisol elevation is associated with hippocampal atrophy. Thus, cortisol levels could be monitored and managed in older people, to decrease their risk of AD type hippocampal dysfunction. We generated an in silicomodel of the chronic effects of elevated plasma cortisol on hippocampal activity and atrophy, using the systems biology mark-up language (SBML). We further challenged the model with biologically based interventions to ascertain if cortisol associated hippocampal dysfunction could be abrogated.  相似文献   
24.
Projection-reconstruction NMR experiments have been shown to significantly reduce the acquisition time required to obtain protein backbone assignment data. To date, this concept has only been applied to smaller (15)N/(13)C-labeled proteins. Here, we show that projection-reconstruction NMR techniques can be extended to larger protonated and perdeuterated proteins. We present a suite of (4,2)D triple-resonance experiments for protein backbone assignment and a Hybrid Backprojection/Lower-Value algorithm for reconstructing data with relatively weak signal-to-noise ratios. In addition, we propose a sampling theorem and discuss its implication on the choice of projection angles. We demonstrate the efficacy of this approach using the 29 kDa protein, human carbonic anhydrase II and the 30 kDa protein, calbindin D(28K).  相似文献   
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Multiple bonds between boron and transition metals are known in many borylene (:BR) complexes via metal dπ→BR back-donation, despite the electron deficiency of boron. An electron-precise metal–boron triple bond was first observed in BiB2O [Bi≡B−B≡O] in which both boron atoms can be viewed as sp-hybridized and the [B−BO] fragment is isoelectronic to a carbyne (CR). To search for the first electron-precise transition-metal-boron triple-bond species, we have produced IrB2O and ReB2O and investigated them by photoelectron spectroscopy and quantum-chemical calculations. The results allow to elucidate the structures and bonding in the two clusters. We find IrB2O has a closed-shell bent structure (Cs, 1A′) with BO coordinated to an Ir≡B unit, (OB)Ir≡B, whereas ReB2O is linear (C∞v, 3Σ) with an electron-precise Re≡B triple bond, [Re≡B−B≡O]. The results suggest the intriguing possibility of synthesizing compounds with electron-precise M≡B triple bonds analogous to classical carbyne systems.  相似文献   
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Multiple bonds between boron and transition metals are known in many borylene (:BR) complexes via metal dπ→BR back‐donation, despite the electron deficiency of boron. An electron‐precise metal–boron triple bond was first observed in BiB2O? [Bi≡B?B≡O]? in which both boron atoms can be viewed as sp‐hybridized and the [B?BO]? fragment is isoelectronic to a carbyne (CR). To search for the first electron‐precise transition‐metal‐boron triple‐bond species, we have produced IrB2O? and ReB2O? and investigated them by photoelectron spectroscopy and quantum‐chemical calculations. The results allow to elucidate the structures and bonding in the two clusters. We find IrB2O? has a closed‐shell bent structure (Cs, 1A′) with BO? coordinated to an Ir≡B unit, (?OB)Ir≡B, whereas ReB2O? is linear (C∞v, 3Σ?) with an electron‐precise Re≡B triple bond, [Re≡B?B≡O]?. The results suggest the intriguing possibility of synthesizing compounds with electron‐precise M≡B triple bonds analogous to classical carbyne systems.  相似文献   
30.
The modulation of metal ions on protein function is well recognized and of paramount importance in protein biochemistry. To date, very few methods allow direct determination of protein-metal ion interactions, as well as exact stoichiometric binding ratios. In this work we demonstrate the usefulness of two on-line size exclusion gel filtration mass spectrometry approaches to directly detect protein-metal ion adducts, as well as determine exact protein-metal ion stoichiometries. We show that on-line size exclusion column chromatography (SEC) and rapid in-line desalting (RILED) coupled to microelectrospray mass spectrometry (microESI-MS) can be used for such analyses. The SEC approach can be effectively used to both separate proteins in a complex mixture and exchange buffers prior to the electrospray process. While RILED does not allow for protein separation, it provides a much faster high-throughput desalting procedure than the conventional SEC technique. Specifically, we show that SEC/microESI-MS and RILED/MS can be used to determine calcium ion binding stoichiometries to a high-affinity, metal ion binding protein, calbindin D(28K). Furthermore, the same approaches can also be used to determine metal ion binding stoichiometries of low-affinity metal-binding proteins such as Spo0F.  相似文献   
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