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排序方式: 共有191条查询结果,搜索用时 15 毫秒
1.
In this paper, we explore the interplay of four different conjectures on certain zero-sum problems in Zp Zp. This study of the inter-relations between these conjectures leads to the conclusion that determining the structure of minimal zero sequences (see below for the precise definition) is crucial. Also, we study the analogous situation in Zn. 相似文献
2.
Critical problems of the present approach of electrolytes for Solid Oxide Fuel Cells (SOFCs) for commercialization are discussed.
Major progress is expected from the development of materials based on the “SEA (Single Element Arrangement)” concept. The
galvanic cell consists in this case basically of a single chemically homogeneous compound, which functions as electrodes at
high and low activity and as electrolyte at intermediate activities of the electroactive component.
In view of the large structural flexibility of the chemical nature of the constitutents, we explored perovskite (ABO3)-type compounds to be used as SEAs for SOFCs. Results of studies on Pr-substituted LSGM and Fe-substituted SrSnO3 perovskite-type oxides are presented. For instance, SrSn1-xFexO3-δ with x=0.1 exhibits p and n-type electronic conduction at the cathode and anode sides of the SOFC, respectively, while oxide
ion conduction prevails at intermediate oxygen partial pressures. The SEA concept is also applicable for other devices in
the field of Ionics. 相似文献
3.
Chanchal Kiran Thakur Rabin Neupane Chandrabose Karthikeyan Charles R. Ashby Jr. R. Jayachandra Babu Sai H. S. Boddu Amit K. Tiwari Narayana Subbiah Hari Narayana Moorthy 《Molecules (Basel, Switzerland)》2022,27(21)
Multiwalled carbon nanotubes (MWCNTs) are elongated, hollow cylindrical nanotubes made of sp2 carbon. MWCNTs have attracted significant attention in the area of drug delivery due to their high drug-loading capacity and large surface area. Furthermore, they can be linked to bioactive ligands molecules via covalent and noncovalent bonds that allow for the targeted delivery of anticancer drugs such as doxorubicin. The majority of methodologies reported for the functionalization of MWCNTs for drug delivery are quite complex and use expensive linkers and ligands. In the present study, we report a simple, cost-effective approach for functionalizing MWCNTs with the carbohydrate ligands, galactose (GA), mannose (MA) and lactose (LA), using lysine as a linker. The doxorubicin (Dox)-loaded functionalized MWCNTs were characterized using FT-IR, NMR, Raman, XRD and FE-SEM. The drug–loaded MWCNTs were evaluated for drug loading, drug release and cell toxicity in vitro, in breast cancer cells. The results indicated that the carbohydrate-modified lysinated MWCNTs had greater Dox loading capacity, compared to carboxylated MWCNTs (COOHMWCNTs) and lysinated MWCNTs (LyMWCNTs). In vitro drug release experiments indicated that the carbohydrate functionalized LyMWCNTs had higher Dox release at pH 5.0, compared to the physiological pH of 7.4, over 120 h, indicating that they are suitable candidates for targeting the tumor microenvironment as a result of their sustained release profile of Dox. Doxorubicin-loaded galactosylated MWCNTs (Dox-GAMWCNTs) and doxorubicin loaded mannosylated MWCNTs (Dox-MAMWCNTs) had greater anticancer efficacy and cellular uptake, compared to doxorubicin–loaded lactosylated MWCNTs (Dox-LAMWCNTs) and pure Dox, in MDA-MB231 and MCF7 breast cancer cells. However, neither the ligand conjugated multiwall blank carbon nanotubes (GAMWCNTs, MAMWCNTs and LAMWCNTs) nor the lysinated multiwalled blank carbon nanotubes produced significant toxicity in the normal cells. Our results suggest that sugar-tethered multiwalled carbon nanotubes, especially the galactosylated (Dox-GAMWCNTs) and mannosylated (Dox-MAMWCNTs) formulations, may be used to improve the targeted delivery of anticancer drugs to breast cancer cells. 相似文献
4.
S. Ramasamy D. J. Smith P. Thangadurai K. Ravichandran T. Prakash K. PAdmaprasad V. Sabarinathan 《Pramana》2005,65(5):881-891
The ultra high vacuum chamber was developed in the Department of Nuclear Physics, University of Madras with the funding from
DST, India. This UHV chamber is used to prepare nanocrystalline materials by inert gas condensation technique (IGCT). Nanocrystalline
materials such as PbF2, Mn2+-doped PbF2, Sn-doped In2O3 (ITO), ZnO, Al2O3, Ag2O, CdO, CuO, ZnSe:ZnO etc., were prepared by this technique and characterized. Results of some of these materials will be
presented in this paper. In solid-state207Pb NMR on PbF2 a separate signal due to the presence of grain boundary has been observed. The structural phase transition pressure during
the phase transformation from the cubic phase to orthorhombic phase under high pressure shows an increase with the decrease
in grain size. Presence of electronic centres in nanocrystalline PbF2 is observed from Raman studies and the same has been confirmed by photoluminescence studies. Al2O3 was prepared and56Fe ions were implanted. After implantation segregation of56Fe ions was examined by SEM. The oxidation properties of ITO were studied by HRTEM. As against the expectation of oxide coating
on individual nanograins of In-Sn alloy, ITO nanograins grew into faceted nanograins on heat treatment in air and O2 atmosphere. The growth of ITO under O2 atmosphere showed pentagon symmetry. The PMN was initially prepared by solid-state reaction. Further, this PMN relaxor material
will be used to convert into nanocrystalline PMN by IGCT with sputtering and will be studied 相似文献
5.
We report the synthesis, structure, microstructure, chemical stability in H2O and CO2, and electrical transport properties of an oxide ion-conducting perovskite-related structure Ba3In2MO8 (M = Zr, Ce, Zr0.5Ce0.5). Powder X-ray diffraction confirmed the formation of a simple cubic perovskite-like structure for Ba3In2ZrO8 (a = 4.205(9) ?), Ba3In2CeO8 (a = 4.234(1) ?), and Ba3In2Zr0.5Ce0.5O8 (a = 4.285(8) ?). The increase in lattice constant is consistent with the Shannon’s ionic radius trend. Among the three samples
investigated, Ba3In2ZrO8 was found to be stable against reaction with pure CO2 at elevated temperature, while the Ce and 1:1 Zr and Ce compounds were unstable at 600 °C. Ba3In2ZrO8, Ba3In2CeO8, and Ba3In2Zr0.5Ce0.5O8 were found to be chemically unstable in H2O at about 50 °C. The bulk electrical conductivity of the samples prepared at different temperatures was found to be nearly
the same; the total conductivity (bulk + grain–boundary + electrode) seems to change with sintering temperature. Both Ba3In2ZrO8 and Ba3In2CeO8, prepared at 1,400 °C, exhibited comparable electrical conductivity of about 6 × 10−3 S cm−1 at 800 °C, which is comparable to that of conventional Y2O3-doped ZrO2 electrolyte. These compounds are very promising electroltes, provided that their chemical and mechnical stabitities are improved
without losing any ionic conductivity. 相似文献
6.
Sheikdawood Parveen Thathan Premkumar Subbiyan Poornima Subbiah Govindarajan 《Journal of Saudi Chemical Society》2019,23(6):691-701
Metal complexes ([ML2], where M = Fe, Co, or Zn; HL = 2-[(6-ethyl-5-oxo-4,5-dihydro-2H-[1,2,4]triazin-3-ylidene)-hydrazono]-butyric acid, C9H13N5O3) of a Schiff base derived from α-ketobutyric acid (α-KBA) and diaminoguanidine (Damgu) were synthesized and characterized using elemental, spectral, and thermal studies. The metal complexes exhibited similar decomposition behavior, with a highly exothermic final decomposition step resulting in the formation of metal oxides. Isomorphism among the complexes was revealed using a powder X-ray diffraction (PXRD) technique. Solid solution precursors ([Zn1/3M2/3(L)2], where M = Fe, Co) were synthesized and characterized using various physico-chemical techniques. A thermal decomposition technique was used to prepare spinel-type zinc cobaltite (ZnCo2O4) and zinc ferrite (ZnFe2O4) nanocrystalline particles with the synthesized single source precursors. Structural studies using PXRD ascertained the predominant crystal phase to be spinel. Transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) showed a mean nanoparticle size of 18 ± 2 nm. Magnetic measurements revealed a weak magnetic behavior in the synthesized spinels. In the aqueous phase, the spinels exhibited catalytic activity, reducing 4-nitrophenol (4-NP) in the presence of NaBH4 at room temperature. Additionally, the study demonstrated that the catalyst can be recovered and reused for five cycles with a more than 85% conversion efficiency. 相似文献
7.
Vidya Rani Chandrasekhar Kesavan Mookkandi Palsamy Ravi Lokesh Daniel Thangadurai T. Indra Gandhi N. Rajesh Jegathalaprathaban Rajagopal Gurusamy 《应用有机金属化学》2019,33(3)
Three new metal complexes [Cu(L)2] (1), [Co(L)2] (2) and [Zn(L)2] (3) have been prepared by the reaction of hydrated salts of metal (II) acetate with new Schiff base ligand HL, [2‐((4‐(dimethylamino)phenylimino)methyl)‐4,6‐di‐t‐butylphenol] and characterized by different physico‐chemical analyses such as elemental analysis, single XRD, 1H NMR, FTIR and UV–Vis spectroscopic techniques. Their biomolecular docking, antimicrobial and cytotoxicity studies have also been demonstrated. The proposed structure of Schiff base ligand HL and complex 2 are confirmed by Single crystal X‐ray crystallography study. This analysis revealed that metal (II) complexes remain in distorted tetrahedral coordination environments. The electronic properties such as HOMO and LUMO energies are carried out by gaseous phase DFT/B3LYP calculations using Gaussian 09 program. Complex 1 showed a good binding propensity to the DNA and HSA, during the assessment of docking studies. Schiff base ligand HL and its metal (II) complexes, 1–3 screened for their in vitro antimicrobial activities using the disc diffusion method against selected microbes. Complex 1 shows higher antimicrobial activity than complexes 2, 3 and Schiff base ligand HL. According to the results obtained from the cytotoxic studies, Schiff base ligand HL and its metal (II) complexes 1–3 have better cytotoxicity against MCF‐7 cell lines with potency higher than the currently used chemotherapeutic agent cyclophosphamide. 相似文献
8.
9.
Tailoring ceramics for specific applications: A case study of the development of all-solid-state lithium batteries 总被引:1,自引:0,他引:1
Metal oxides with the nominal chemical compositions Li5La3M2O12 (M=Nb, Ta), possessing a garnet-like structure, exhibit ionic bulk conductivities of the order of magnitude of ∼10−6 S/cm at 25 °C. Partial substitution of La by alkaline earth elements (Ca, Sr, Ba) in Li5La3M2O12 yields new members of compounds with garnet-like structure with the composition Li6ALa2M2O12 (A=Ca, Sr, Ba). Among the investigated compounds, so far, the Ba-compound Li6BaLa2Ta2O12 exhibits the highest bulk conductivity of 4.0×10−5 S/cm at 22 °C with an activation energy of 0.40 eV. All Ta-members were found to be stable against chemical reaction with
molten elemental lithium. Li6ALa2Ta2O12 (A=Sr, Ba) exhibit also high electrochemical stability of ∼6 V vs. lithium and chemical stability against reaction with LiCoO2 cathode material.
A novel high voltage thin-film battery was constructed using spinel-type Li2MMn3O8 (M=Co, Fe) as positive electrode, LiPON as electrolyte and Al as negative electrode material. Li2MMn3O8 (M=Fe, Co) electrodes show two reversible plateaus during the charging and discharging cycle at ∼4 and ∼5 V vs. Li. The former
plateau is due to the valence change of Mn3+ to Mn4+ and the latter one is due to the oxidation of M3+ to M4+. The chemical diffusion coefficient (
) was found to be in the range 10−13–10−12 cm2/sec for any composition x of Li2−xMMn3O8 (M=Fe, Co) in the range from 0.1 to 1.6 by employing the galvanostatic intermittent titration technique (GITT). AC impedance
studies revealed an electrolyte-electrode charge transfer resistance of 260–290 Θ and an electrode double layer capacity of
∼45–70 μF for an electrode area of 6.7 cm2 at room temperature. The chemical diffusion coefficient of the Al,LiAl negative electrode is about three orders of magnitude
higher than that of the positive electrode materials. Accordingly, we believe that the diffusion of Li into and out of the
cathode material is the rate determining process.
Paper presented at the Patras Conference on Solid State Ionics - Transport Properties, Patras, Greece, Sept. 14 – 18, 2004. 相似文献
10.
Subbiah Meenakshisundaram RM. Sockalingam 《Journal of molecular catalysis. A, Chemical》2000,160(2):269-275
Catalytic activity of Os(VIII) in the oxidation of some twenty organic sulfides with sodium salt of N-chlorobenzenesulfonamide (CAB) has been investigated in alkaline (pH8.7) t-butanol–water (1:1 v/v) medium. Significant retarding influence of [OH−] on the reactivity is exhibited. The catalysed reaction is strongly accelerated in the presence of Hg(II). Imperfections are observed in the linear Hammett relationship in the case of –NO2 substituents. 相似文献