亚波长金属/电介质双层光栅偏振片

用严格耦合波分析亚波长金属光栅和高频电介质光栅的衍射性质,给出了亚波长金属/电介质双层光栅偏振片的设计,同时通过严格耦合波分析给出了这种偏振片的TM波的反射特性和反射偏振比.     

透射型亚波长二元闪耀光栅的数值模拟与分析

使用OptiFDTD对透射型亚波长二元闪耀光栅的透射场进行了数值模拟;使用FFT方法对电磁场分量进行分析,得到其各个级次的能量分布,进而分析了亚波长结构二元光栅的各个参数对衍射性能的影响。分析结果证实:透射型亚波长二元闪耀光栅可将正入射的TE波闪耀到 1级,且等分数对衍射角影响很小。给定波长,其设计主要由光栅周期、光栅材料折射率和等分数这3个参数决定。     

Observation of small-scale processes over shelf break in the East China Sea

The turbulent dissipation along with temperature and salinity was measured on board R/V Dong Fang Hong 2 over the shelf break of the East China Sea from March 7 to 9, 2004. Applying the Turner angle, it is found that the ＇diffusive＇ double diffusion, salt-fingering, and stable stratification coexist in the upper water column of about 50 m. Below that depth, there exists weak salt-fingering. The turbulent dissipation rates are enhanced along the ray paths of M2 internal tides emanating from the shelf break with values ranging from 1.0×10^-9 W·kg^-1 to 1.2×10^-6 W·kg^-1. The corresponding diapycnal mixing rates are from 1×10^-6 m^2· s^-1 to 1×10^-2 m^2· s^-1. The spatially averaged mixing rate over the whole observation section is 2.3×10^-3 m^2· s^-1, which is much larger than 1×10^-5 m^2·s^-1 of the background diapycnal mixing rate in the open ocean.     

Comparison of infection of different cell lines by uropathogenic Escherichia coli

Studying the interaction between uropathogenic Escherichia coil （UPEC） and uroepithelial cells is important in elucidating the pathogenesis of urinary tract infection. In this study, the African green monkey kidney cells （Vero）, human kidney carcinoma cells （Ketr-3） and bladder carcinoma cells （EJ） were infected by UPEC132, a clinical strain isolated from Tianjin, China, and were compared for their capacities to allow the adherence and invasion by this strain. The results revealed that all these cell lines could be attached and invaded by UPEC132. The adherence rates for Vero, Ketr-3 and EJ cells were （49,20 ±7.55）%, （55.22 ±4.09）% and （73.20 ±5.26）%, respectively, and invasion frequencies were （2.61 ±0.32）×10^-3, （3.00 ±0.34）×10^-3 and （3.25 ± 0.20）×10^-3, respectively. The statistical analysis showed that the adherence rate for EJ cells was significantly higher than those for the other two cell lines （P〈0.05）, and the invasion frequencies for EJ and Ketr-3 cells had no statistical differences （P〉0.05） but were higher than that for Vero cells （P〈0.05）. Three cell lines were detected for the receptors for P pill of UPEC by using indirect immunofluorescence. The results showed that receptors existed on the surfaces of all cell lines, and the highest distribution was found on the surface of EJ cells. Additionally, the invasion of EJ cells by recombinant UPEC132/pSELECT-GFP could be directly visualized using confocal microscopy. These data strongly implicated that EJ cells could be more easily infected by UPEC132 than the other cells, and thus could serve as a good experimental target for further investigation of UPEC infection.     

Carbon sequestration within millet phytoliths from dry-farming of crops in China

Phytoliths are noncrystalline minerals that form inside cells and cell walls of different parts of plants. Organic carbon in living cells can be occluded in phytoliths during plant growth. It has been documented that the occluded carbon within phytoliths is an important long-term terrestrial carbon reservoir that has a major role in the global carbon cycle. Common millet and foxtail millet have become typical dry-farming crops in China since the Neolithic Age. The study of carbon conservation within phytoliths in these crops could provide insights into anthropogenic influences on the carbon cycle. In this study, we analyzed the carbon content in phytoliths of common millet and foxtail millet. The results indicated that (1) common millet and foxtail millet contained 0.136% ± 0.070% and 0.129% ± 0.085% phytolith-occluded carbon (PhytOC) on a dry mass basis, respectively; (2) based on the mean annual production of common millet and foxtail millet in the last 10 years, the phytolith occluded carbon accumulation rate of common millet and foxtail millet was approximately 0.023 ± 0.015 and 0.020 ± 0.010 t CO 2 ha 1 a 1 , respectively; (3) assuming a similar phytolith occluded carbon accumulation rate as for common millet (the highest accumulation rate was 0.038 t CO 2 ha 1 a 1 ), this could result in the sequestration of 2.37 × 10 6 t CO 2 per year for the 62.4 × 10 6 ha dry-farming crops in China. Although there was a decline in the annual production rate and planting area of foxtail millet during 1949 to 2008, the total phytolith carbon sequestration rate was 7×10 6 t CO 2 within the 60-year period. However, phytolith occluded carbon has not yet been fully considered as a global carbon sink. Also, this carbon fraction is probably one of the best candidates for the missing carbon sink.     

Rate constants for the reaction of ozone with <Emphasis Type="Italic">n</Emphasis>-butyl, <Emphasis Type="Italic">s</Emphasis>-butyl and <Emphasis Type="Italic">t</Emphasis>-butyl methyl sulfides

The rate constants for the ozone reactions with n-butyl methyl sulfide （n-BMS, CHaCH2CH2CH2SCH3）, sec-butyl methyl sulfide （s-BMS, CH3CH2（CH3）CHSCHa） and tert-butyl methyl sulfide （t-BMS, （CH3）3CSCH3） were measured using our smog chamber under supposedly pseudo-first-order conditions at 30002 K and 760 Torr. The experimental determined rate constants for n-butyl, s-butyl and t-butyl methyl sulfide are （1.23 ± 0.06）×10-19, （5.08 ± 0.19）×10-20 and （2.26 ± 0.14）×10-20 cm3 molecule-1· s-1, respectively. The reactivity-structure relationship of the reactions was discussed and used to illustrate the mechanism of the ozone reaction with thioethers. The results enrich the kinetics data of atmospheric chemistry.     

Chirped Bragg 光纤光栅色散补偿研究

分析ＣｈｉｒｐｅｄＢｒａｇｇ光纤光栅的色散特性，并作一定性分析．利用耦合模方程导出ＣｈｉｒｐｅｄＢｒａｇｇ光纤光栅的反射率方程，从而推导出ＣｈｉｒｐｅｄＢｒａｇｇ光纤光栅的色散计算公式，并用数值分析画出它们的响应曲线．     

Experimental investigation of incremental reactivity of di-tert-butyl peroxide

Large quantities of di-tert-butyl peroxide (DTBP) have been emitted into the troposphere due to human activities. Its role in the atmospheric photochemical reaction has not been understood. This study presents the results of the photochemical reactions of DTBP and NOx, which have been simulated in a self-made smog chamber under the temperature of (29±1)℃. Both the wall decays of ozone and NO2 could be neglected, compared to the results in simulative experiments. The effective intensity of UV light used in the experiments was 1.28×10-3 s-1, which was expressed by the rate constant of NO2 photolysis in purified air. The reaction mechanism was proposed according to our results and reports of other researchers. The maximum values of incremental reactivity (IR) in the three simulative ex- periments were 9.53×10-2, 5.23×10-2 and 3.78×10-2, respectively. The incremental reactivity decreased with the increase of initial concentrations of DTBP. The IR value of DTBP obtained in this study was comparable to that of acetylene reported in our previous research.     

Binding and endocytosis of monoterbium transferrin by K562 cells

Human serum apotransferrin is the major iron-tran- sport protein in blood. The protein binds iron as Fe3+ at two similar, but not identical, high-affinity binding sites. Although iron bound to human serum apotransferrin is less then 0.1% (~3 mg) of the total body iron, dynamically it is the most important iron pool with the highest rate of turnover. The turnover of transferrin iron is in the order of 30 mg per day and, normally, about 80% of this iron are transported to the bone marrow for hem…     

Kinetic study of the reaction of chlorine atoms with 3-methyl-3-buten-1-ol

The reaction of a typical unsaturated alcohol, 3-methyl-3-buten-1-ol （MBO331）, with Cl atoms, was investigated for the first time. The reaction was investigated using discharged flow-tube coupled with electron impact mass spectrometer. The experiments were performed over the temperature range of 248 K-298 K and at pressure of 1 torr in He as the bath gas. The obtained kinetic data were used to derive the Arrhenius expression： k1 = （3.47 ± 1.21） × 10^-11 exp[（ 599 ±69）/7] cm^3 molecule^-1 s^-1. Finally, atmospheric lifetimes of the MBO331 with respect to OH radicals, NO3 radicals and CI atoms have been calculated and the atmospheric implications are considered briefly.     

Investigation of Ru （ phen ）3^2＋-Hydrazine-Ce（Ⅳ） Chemiluminescence System and Its Analytical Application

0 IntroductionThbiep ycroidmipnlee)xru ctahteinoinu mof(Ⅱ r)u t(he Rniuu(mbip,y m)3ai2n +ly) atrnids- t(r2is -,(21’ -,10-phenanthroline)ruthenium(Ⅱ) (Ru(phen)32 +) ,is a kindof sensitive analytical reagent for electrogenerated chemilumi-nescence(ECL) and chemiluminescence(CL) ,on which a par-ticular review has been presented[1]. The earliest publicationon the synthesis of Ru(bipy)32 +appeared in 1936[2], andduringthefollowing30 years ,theinvestigations relatedtothissubstance were only in…     

A novel high-sensitivity pressure sensor: Thinned fiber Bragg grating with pressure-sensing polymer

Based on thinned fiber Bragg grating and polymer material, we propose a novel high-sensitivity pressure sensor and obtained a new contribution to the pressure sensitivity, which is dependent on the derivative of the effective refractive index (RI) of core mode with respect to the surrounding medium RI, as well as on the relationship between the polymer RI and the pressure; moreover, it is inversely proportional to Young’s modulus of the polymer material. For the polymer with Young’s modulus of 1.0 MPa, the total pressure sensitivity 1.54×10-2 MPa-1 can be obtained.     

Determination of isocarbophos by cathodically sweeping oscilliopolarography

Determination of isocarbophos by cathodically sweeping oscilliopolarography is described. In a 1.0×10⁻⁵ mol/L sodium dodecylbenzene sulfonate (SDS)+0.1 mol/L HAC-NaAC (pH=4.0) buffer medium, isocarbophos and its alkaline hydrolysate exhibited sensitive second derivative wave at −0.50 V and −0.48 V respectively. The peak current was linearly proportional to the concentration of isocarbophos in the range of 5.40×10⁻⁶−1.05×10⁻⁴ mol/L by detecting isocarbophos directly. The detection limit was 3.60×10⁻⁶ mol/L with the relative standard derivation (RSD) of 7.3%. By employing an alkaline hydrolysis, the peak current was linearly proportional to the concentration of isocarbophos in the range from 7.70×10⁻⁷ mol/L to 1.24×10⁻⁴ mol/L, and the detection limit was 5.80×10⁻⁷ mol/L with RSD of 3.1%. The hydrolysis procedure and the electrode reaction were studied by voltammetry. Foundation item: Supported by the Foundation of Chinese-France Cooperation Program on Advanced Research Biography: ZHANG Wu-ming (1929-), female, Professor.     

Organic media enhanced spectrofluorimetric determination of L-ascorbic acid

A novel spectrofluorimetric method for the determination of L-ascorbic acid is proposed. It is based on the inhibition of L-ascorbic acid on the formation of 2,3-diaminophenazine, which is an oxidation product ofo-phenylenediamine catalyzed by laccase. The fluorescence (at λ_cx/λ_cm=464 nm /530 nnm) was enhanced strongly in the presence of organic media. The mechanism ofo-phenylenediamine oxidation reaction catalyzed by laccase in the presence of L-ascorbic acid is discussed. L-ascorbic acid is determined in the ethanol, 1,4-dioxane and acetone over the linear range of 4.0×10⁻⁷≈1.2×10⁻⁴ mol/L, 4.0×10⁻⁷≈8.0×10⁻⁵ mol/L and 4.0×10⁻⁷≈1.0×10⁻⁴ mol/L with a detection limit of 1.20×10⁻⁵ mol/L, 1.19×10⁻⁵ mol/L and 1.24×10⁻⁸ mol/L, respectively. The method has been successfully applied to the simple and rapid determination of L-ascorbic acid in pharmaceuticals and milk powder. Supported by National Natural Science Foundation of China and the Special Funds of State Education Committe for Doctorate Research Huang Zuyun: born in Aug. 1963. Ph.D     

Investigation of the cross-reaction mechanism of C<Subscript>6</Subscript>H<Subscript>5</Subscript>F-HNO<Subscript>2</Subscript> aqueous solution irradiated at 355 nm by transient absorbance spectrum technique

The transient absorption spectrum technique was employed to investigate the cross-reaction mechanism of C6H5F-HNO2 aqueous solution irradiated at 355 nm. The characteristic and the kinetic parameters of transient species were also detected. Hydroxyl radical derived from the photolysis of HNO2 was added to monofluorobenzene with a second-order rate constant of （5.83±0.17）×10^9 L·mol^-1·s^-1 to form an adduct, C6H5F…OH, which was able to react with HNO2 as the main reaction pathway with a rate constant of （8.3±0.1）×10^7 L·mol^-1·s^-1. The C6F6…OH adduct can also be decayed by elimination of H2O to yield monofluorophenyl radical C6H4F-. By GC-MS technique, the final products were identified to be monofluorophenol, nitro-monofluorobenzene, nitro-monofluorophenol and para-fluorobiphenyl.     

Photonic engineering. Aphrodite's iridescence

The most intense colours displayed in nature result from either multilayer reflectors or linear diffraction gratings. Here we investigate the spectacular iridescence of a spine (notoseta) from the sea mouse Aphrodita sp. (Polychaeta: Aphroditidae). The spine normally appears to be deep red in colour, but when light is incident perpendicular to the axis of the spine, different colours are seen as stripes running parallel to the axis of the spine; over a range of smaller incident angles, the complete visible spectrum is reflected with a reflectivity of 100% to the human eye. The simple structure responsible for this effect is a remarkable example of photonic engineering by a living organism.     

Isotopic composition of helium in eclogite from the Dabie Mountains, central China and its geological significance

Isotopic geochemical characteristics of helium in garnet and omphacite of eclogite in the Dabie Mountains are discussed. Concentrations of³He and⁴He in garnet and omphacite are 3.9 × 10⁻¹⁴–24.0 × 10⁻¹⁴ and 0.48 × 10⁻⁷–9.42 × 10⁻⁷cm¹³.g⁻¹, respectively. Values of³He/⁴He have a range of (1.19–4.63) × 10⁻⁷. Helium In the eclogite is derived from both mantle and crust. Isotopic geochemical data of helium indicate that eclogite in the Dabie Mountains might be formed in depleted mantle and the age of the cologite would be Indo-China epoch.     

Voltammetric Response of Epinephrine at Carbon Nanotube Modified Glassy Carbon Electrode and Activated Glassy Carbon Electrode

0Introduction Epinephrine(EP)isanimportantcate cholamineneurotransmitterinthemammaliancentralnervoussystem,whichissecretedbythesu prarenalglandalongwithnorepinephrine.Itisgen erallyusedtotreathypertension,bronchialasthma,organicheartdisease,andincardiacsurgeryand myocardialinfarction[1].VariousmethodshavebeendevelopedforEPstudy,suchascapillaryelectro phoresis(CE)[2],highperformanceliquidchroma tography(HPLC)andflowinjectionanalysis(FIA)[3].Numerousobservationsontheelectro chemicalbehavio…     

Effect of Dy3+on osteogenic and adipogenic differentiation of mouse primary bone marrow stromal cells and adipocytic trans-differentiation of mouse primary osteoblasts

A series of experimental methods including 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) test, alkaline phosphatase (ALP) activity measurement, mineralized function, Oil Red O stain and measurement were employed to assess the effect of Dy³⁺ on the osteogenic and adipogenic differentiation of mouse primary bone marrow stromal cells (BMSCs) and the adipogenic trans-differentiation of mouse primary osteoblasts (OBs). The results showed that Dy³⁺ had no effect on BMSC proliferation at concentrations of 1×10⁻⁸ and 1×10⁻⁵ mol/L, but inhibited BMSC proliferation at other concentrations. Dy³⁺ had no effect on OB proliferation at concentrations of 1×10⁻¹⁰ and 1×10⁻⁹ mol/L, but inhibited OB proliferation at other concentrations. Dy³⁺ had no effect on the osteogenic differentiation of BMSCs at concentrations of 1×10⁻⁹ and 1×10⁻⁷ mol/L, and promoted osteogenic differentiation of BMSCs at other concentrations at the 7th day. The osteogenic differentiation of BMSCs was inhibited by Dy³⁺ at concentration of 1×10⁻⁵ mol/L at the 14th day, but promoted osteogenic differentiation of BMSCs at concentrations of 1×10⁻⁹, 1×10⁻⁸, 1×10⁻⁷ and 1×10⁻⁶ mol/L with the maximal effect at concentration of 10⁻⁶ mol/L. Dy³⁺ promoted mineralized function of BMSCs at any concentration. Dy³⁺ had no effect on adipogenic differentiation of BMSCs at concentration of 1×10⁻⁷ mol/L, but inhibited adipogenic differentiation of BMSCs at other concentrations. Dy³⁺ inhibited adipocytic trans-differentiation of OBs at any concentration, suggesting that Dy³⁺ had protective effect on bone and the protective effect on bone may be mediated by modulating differentiation of BMSCs away from the adipocyte and inhibiting adipocytic trans-differentiation of OBs which may promote differentiation and mineralization of OBs. These results may be valuable for better understanding the mechanism of the effect of Dy³⁺ on pathogenesis of osteoporosis. Supported by the Foundation for Key Program of Ministry of Education of China (Grant No. 208018)     

Trace determination of zirconium using anodic adsorptive voltammetry at a carbon paste electrode modified with multi-walled carbon nanotubes

A carbon paste electrode modified with multi-walled carbon nanotubes （MWCNT） was prepared and the determination of ultra trace amount of zirconium based on the anodic adsorptive voltammetry of the zirconium-calcium-alizarin red S mix-polynuclear complex is described in this paper for the first time. The results showed that the sensitivity and the selectivity of the method are excellent. The second derivative linear scan voltammograms of the complex were recorded by polarographic analyzer from 200 to 1200 mV （vs. SCE） and it was found that the complex can be adsorbed on the surface of the electrode, yielding a peak at about 840 mV, corresponding to the oxidation of ARS in the complex. The peak current increases linearly with Zr （IV） concentration in the range of 6.0×10^-12--6.0×10^-11 mol. L^-1 （accumulation time 120 s）, 6.0×10^-11--2.0×10^-9 mol. L-1 （accumulation time 90 s） and 2.0×10^-9--1.0×10^-7 mol. L^-1 （accumulation time 60 s） and the detection limit （S/N = 3） is 2.0×10^-12 mol. L^-1 （accumulation time 180 s）. The procedure has been successfully applied to the determination of zirconium in the ore samples.