Sol-gel deposition of calcium silicate red-emitting luminescent films doped with Eu3+

Eu3+-activated calcium silicate (CaO-SiO2:Eu3+) luminescent films were prepared by the sol-gel method. The structural evolution of the film was studied by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), and the luminescence properties of the phosphor films were investigated as a function of heat treatment temperature. The XRD study indicates that a kilchoanite phase forms in the film sintered at 800 degreesC, which is different from that in gel powder treated under the same conditions. The SEM results show that the film thickness decreases and the particles in the film become smaller with increasing heat treatment temperature. The CaO-SiO2:Eu film shows the characteristic emission of Eu3+ under UV excitation, with the Eu3+ D-5(0)-->F-7(2) band (616 nm) being the most prominent. A large difference in the Eu3+ lifetime is observed between the film samples treated at 500 and 700 degreesC (or above). Concentration quenching occurs when the Eu3+ doping concentration is above 6 mol% of Ca2+ in the film.

Calculation of chemical bond parameters in RBa2Cu4O8(R = Dy,Ho,Er,Tm,Yb) and Y2Ba4Cu7O14.3

Chemical bond parameters in RBa2Cu4O8(R = Dy, Ho, Er, Tm, Yb) and Y2Ba4Cu7O14.3 were calculated by using complex chemical bond theory. The results indicated that the bond covalency in CuO chain was larger than that in CuO2 plane. For metal atoms, the bond covalency of five coordinated case was larger than that of six coordinated case.

RBa_2Cu_4O_8(R=Dy,Ho,Er,Tm,Yb)和Y_2Ba_4Cu_7O_(14.3)的化学键参数计算

使用复杂晶体上化学键理论计算了 RBa2 Cu4 O8(R=Dy,Ho,Er,Tm ,Yb)和 Y2 Ba4 Cu7O14 .3 的化学键参数 .结果表明 ,Cu O链上的 Cu O键共价性大于它们在 Cu O2 面的共价性 .当金属元素与氧形成五配位时 ,其共价性的数值大于这些元素在六配位时的情形

The site symmetry of Eu3+ in ZnS : Eu nanoparticle

Nanosized ZnS doped with different concentrations of Eu3+ were prepared and analyzed by x-ray diffraction technique. The experimental results show that ZnS belongs to the cubic structure. From the photoluminescence (PL) emission spectra, it can be seen that the ratio of the emission intensity of Eu3+ 616 nm to that at 590 nm increases as the increasing of Eu3+. This phenomenon reveals that the site symmetry of Eu3+ reduces as the increasing of Eu3+.

[Ni(C10H8N2)(3)](2)[V4O12].11H(2)O

The crystal structure of the title compound, bis[tris(2,2'-bipyridyl-N,N')nickel(II)] cyclo-tetravanadate undecahydrate, contains a centrosymmetric [V4O12](4-) anion, which has an eight-membered ring structure formed by four VO4 tetrahedra sharing vertices, and two complex cations containing octahedrally-coordinated Ni-II ions. The anion and coordinated Ni-II ions are isolated and make up anion and cation layers, respectively. The Ni-N distances range from 2.077(3) to 2.112(2)Angstrom and the V-O distances range from 1.621(2) to 1.803(2)Angstrom.

Role of Lithium in Multicomponent Oxide Catalysts for Oxidative Coupling of Methane

The effect of Li content in a series of multicomponent oxides LixLa0.5Ti0.5 For methane oxidative coupling has been studied. The catalytic activities of LiLa0.5Ti0.5 catalyst before and after washing with boiling water have been compared. The surface and

锂在甲烷氧化偶联多元氧化物催化剂中的作用

考察了不同Li含量对LixLa0．5Ti0．5系氧化物催化剂的甲烷氧化偶联催化性能的影响；比较了水洗前后LiLa0．5Ti0．5氧化物催化剂的催化活性，并通过XRD、IR、XPS和BET等方法时催化剂进行表征。确认了Li在含稀土、过渡金属多元氧化物中的作用。其中，表面Li的作用是缩小催化剂的比表面积，覆盖表面深度氧化活性位，提高C2选择性；体相Li的作用是部分取代Ti3+进入LaTiO3晶格形成LaTi1-yLiyO3-λ活性相，产生甲烷氧化偶联Li+－O-－Ti3+缺陷簇。（注：LixLa0．5Ti0．5和LiLa0．5Ti0．5表示该系列氧化物催化剂制备时的各金属元素的配比。用来表示催化剂的名称，并不表示实际存在的物相，以下类同，下面出现时，不再加以说明。

THE CLEAVAGE REACTION OF THE MO-MO TRIPLE BOND - THE CRYSTAL-STRUCTURES OF MOLYBDENUM COMPLEXES [CPMO(CO)(2)(C(5)H(4)NS)], [CPMO(CO)(2)(C(9)H(6)NS)]O=PPH(3) AND [CPMO(CO)(2)(S(2)CNME(2)]

The reactions of [Cp2Mo2(CO)4] (1) with 2,2'-dipyridyl disulphide (C5H4NS-)2, 8,8'-diquinolyl disulphide (C9H6NS-)2 and tetramethyl thiuram disulphide (Me2NC(S)S-)2 in toluene solution resulted in the cleavage of the Mo-Mo triple bond to yield molybdenum complexes [CpMo(CO)2(C5H4NS)] (2), [CpMo(CO)2(C9H6NS)] (3) and [CpMo(CO)2(S2CNMe2)] (4), respectively. The molecular structures of 2, 3 . O=PPh3 and 4 were determined by X-ray diffraction studies. Crystals of 2 are monoclinic, space group P2(1)/n, with Z = 4, in a unit cell of dimensions a = 6.448(1), b = 12.616(2), c = 14.772(2) angstrom, beta = 92.85(1)-degrees. The structure was refined to R = 0.028 and R(w) = 0.039 for 1357 observed reflections. Crystals of 3 . O=PPh3 are triclinic, space group P1BAR, with Z = 2, in a unit cell of dimensions a = 11.351(3), b = 13.409(3), c = 9.895(2) angstrom, alpha = 94.59(2), beta = 90.35(2), gamma = 78.07(2)-degrees. The structure was refined to R = 0.033 and R(w) = 0.037 for 3260 observed reflections. Crystals of 4 are monoclinic, space group P2(1)/a and Z = 4 with a = 12.468(5), b = 7.637(2), c = 13.135(4) angstrom, beta = 96.62(3). The structure was refined to R = 0.032 and R(w) = 0.042 for 1698 observed reflections. Each of complexes 2-4 contains a cyclopentadienyl ligand, a cis pair of carbonyls and a chelate ligand (S,N donor or S,S donor). All the compounds have distorted square-pyramid structures.

(η~5-C_5H_5)_2Yb(THF)_2的新合成方法及其晶体结构

双(环戊二烯基)镱(Ⅱ)四氢呋喃配合物(η~5-C_5H_5)_2Yb(THF)_2通过环辛二烯基钾(KC_8H_(11))还原(C_5H_5)_2YbCl·THF而得到,经元素分析、红外光谱表征,并测定了其晶体结构。配合物属单斜晶系,C2/c空间群,晶体学参数a=1.3564(4),b=0.9569(3),c=1.4747(6)nm;β=109.90(3)°;V=1.79975(118)nm~3;D_c=1.65·cm~(-3);μ_C=54.7cm~(-1)(Mo);F(000)=880,Z=4。最后一致性因子R=0.079,R_w=0.081。Yb~(2+)的配位数为8。

SYNTHESIS AND CRYSTAL-STRUCTURE OF HETEROPOLY MOLYBDOSILICIC LANTHANIDE K10H3[PR(SIMO11O39)2].18H2O

The intensity data of the title complex were collected at a low temperature of -90-degrees-C. The compound crystallizes in the monoclinic space group P2(1)/n, a = 17.504(2), b = 27.323 (5), c = 21.616(4) angstrom, beta = 104.49 (2)degrees, Z = 4. The structure was solved by Patterson and Fourier techniques and refined by least-squares to an R = 0.088 for 8320 independent reflections. The central Pr ion is bonded to eight oxygen atoms from two molybdosilicic heteropoly ligands to form a square antiprism. The Pr-O average distance is 2.44 (2) angstrom. Both molybdosilicic heteropoly ligands are of a defective alpha-Keggin structure.

稀土钼硅杂多酸根配合物K_(10)H_3[Pr(SiMo_(11)·O_(39))_2]·18H_2O的合成及晶体结构

本文采用低温技术,在—90℃的干燥氮气保护下,收集标题化合物晶体的衍射数据,用重原子法解出结构。P2_1/n空间群,a=17.504(2),b=27.323(5),c=21.616(4),β=104.49(2)°,z=4.8320个衍射参与精修,最后的R值为0.088。中心离子Pr(Ⅲ)同2个钼硅杂多酸根中的8个氧原子键合,形成正方反棱柱配位多面体。Pr—O的平均键长为2.44(2)。钼硅杂多酸根配体具有缺位的α型Keggin结构。

Fine sediment resuspension dynamics in Moreton Bay

A comprehensive field study has been undertaken to investigate sediment resuspension dynamics in the Moreton Bay, a large semi-enclosed bay situated in South East Queensland, Australia. An instrumented tripod, which housed three current meters, three OBS sensors and one underwater video camera, was used to collect the field data on tides, currents, waves and suspended sediment concentrations at four sites (Sites 1, 2, 4, and 5) in the bay. Site I was located at the main entrance, Site 2 at the central bay in deep water, and Sites 4 and 5 at two small bays in shallow water. The bed sediment was fine sand (d(50) = 0. 2 mm) at Site 1, and cohesive sediment at the other three sites. Based on the collected field data, it is found that the dominant driving forces for sediment resuspension are a combination of ocean swell and tidal currents at Site 1, tidal currents at Site 2, and wind-waves at Sites 4 and 5. The critical bed shear stress for cohesive sediment resuspension is determined as 0. 079 Pa in unidirectional flow at Site 2, and 0. 076 Pa in wave-induced oscillatory flow at Site 5.

热浸镀钢材在海水中的氢渗透行为及其对材料力学性能的影响

氢渗透和拉应力的联合作用对海洋环境中的热浸镀钢材的安全构成潜在威胁，本文以当前应用最广泛的三种商业化热浸镀钢材（Galvanized、Galfan和Galvalume）为研究对象，采用边界元方法计算了三种镀层缺陷周围的电场分布；设计了专用子母配套双电解池并测试了氢渗透电流密度曲线，比较了镀层氢渗透抑制性能及存在缺陷时的自渗氢倾向，并结合镀层成分及结构进行了分析；推导了氢渗透过程相关公式，建立了适合于评价镀层材料氢渗透行为的TANG-LI模型并计算了控制氢渗透相关过程的动力学参数；通过SSRT比较、分析了镀层材料充氢与无充氢条件下的应力－应变行为，并配合断口的显微分析，探讨了海水中带缺陷镀层的氢渗透行为对钢材基体力学性能的影响，结果表明： ⑴海水中三种镀层钢材缺陷处的阴极电位负于析氢电位，能够发生析氢反应而析出氢原子； ⑵ Galvanized镀层对氢渗透的抑制能力较弱，Galfan镀层完好时能明显抑制外部氢的进入，两者存在缺陷时都能产生额外的氢；Galvalume镀层具有很强的氢渗透抑制能力，而且当其存在缺陷时无自渗氢行为；镀层铝含量越高，完整镀层的氢渗透抑制能力越强，缺陷镀层自渗氢能力越弱。 ⑶Galvanized镀层在海水中的氢渗透能降低基体材料的强度并使得其断裂方式由韧性变为准解理，从而加大了材料发生氢脆的倾向；Galfan镀层的氢渗透行为能降低材料的强度但不会改变其韧性断裂方式；Galvalume缺陷镀层则对材料的强度和韧性断裂方式都不能造成影响。