Sol-Gel Synthesis and Luminescent Characteristic of Doped Eu~ 3+ Silicate-Silica Phosphor

Eu-doped silicate complex gel nano-particles was obtained by sol-gel process and characterized with TEM, XRD, PL, etc. The well dispersed particles have particle size about 60 - 70 nm with specific surface area 98.3 m^2· g^- 1 The complex gel phosphor gives a broad and strong luminescent emission originating from Eu^2＋ ions centered at 425 nm. The emission band shifts to shorter wavelengths with the increase of the ion radius of the alkali earth metals, but the band becomes red-shifted gradually with the increase of the ion radius of the alkali metals（except Li ^＋ ）. These divalent Eu^2＋ ions originate in inequivalent substitution of the alkaline earth ions. The presence of alkaline ions is favorable for the increasing emission intensity of the Eu^2 ＋ and lowering crystalline temperature of the silicate complex gel.

Morphology of metal nanoparticles photodeposited on TiO_2/silical gel and photothermal activity for destruction of ethylene

The morphology of supported metal nanoparticles on TiO2/silical gel （TSO） and photothermal synergism were investigated for destruction of ethylene. During photocatalytic deposition of metal nanopartilces, the effects of pH and light intensity on the morphology of coated platinum, palladium, gold on TiO2/silical gel were studied. Moreover, these catalysts were characterized by TEM, UV-Vis DRS. The pH of preparing solution have strong influence on dispersion, size and sites of Pt, Pd and Au on TSO, which were controlled by the electrostatic binding of HPtCl5^- AuCl4^- and TiOH2^＋, Pd^2＋ and TiO^- respectively. Platinum, gold and palladium nanoparticles were uniformly highly dispersed on the titanol sites not silanol of TiO2/silical gel under pH=2, pH =9.9 respectively. For the photodegradation of ethylene, they show higher photothermal efficiency than those prepared with other pH conditions under UV illumination in a non-circulating photoreactor. The optimum weight loadings of Pt, Au, and Pd were 0.25 wt%, 0.5 wt%, 1 wt%, respectively. The synergistic effect enhanced ethylene removal and CO2 production. Thcse results verify that the best photothermal synergistic effect depends on the dispersion, size of noble metal nano-particles. FTIR analyses of the used Pt-, Pd-TSO catalysts indicated that no significant by-products were accumulated on the surface of the catalysts, leading to them longer lifetime.

Microstructure of β-Dicalcium Silicate after Accelerated Carbonation

The present work presents the microstructure of β-Ca_2SiO_4(β-C_2S) after accelerated carbonation. The synthesis procedure of β-C_2S was examined first, and the crystalline and amorphous structure, the distribution and the pore structure of β-C_2S carbonation products were also determined by X-ray diffraction(XRD) quantitative analysis, simultaneous thermal analyzer(TG/DTA), Fourier transform-infrared spectroscopy(FT-IR), high resolution ^(29)Si magic angle spinning nuclear magnetic resonance(^(29)Si NMR), N_2-sorption techniques, and scanning electron microscopy(SEM), respectively. Test results indicate that carbonation products are dramatically formed in the initial 2 h. The main carbonation products are crystalline calcite and amorphous three-dimensional network silica gels, which contain nanometer-sized pores. The calcite, silica gels and un-carbonated β-C_2S are distributed hierarchically.

Research and Advances of Silicate Plugging Agent in the Oilfields

The paper overviews the research and application of silicate plugging agent, according to the different mechanisms and application forms, the plugging agent is divided into silicate gel, silicate precipitation, silicate/polymer, silicate/surfactant, silicate gel/foam and so on. This paper chiefly introduces the conception, mechanism and development tendency of the different systems mentioned above. The development tendency manifests as fully utilize personal properties and cooperate with other plugging agents or technologies, including the study of reaction mechanism, combination of plugging agent, grasping water flood timing, developing deep profile control and water shutoff technology, combining with other measures (chemicals huff and puff), in order to play the role of such blocking agents, further enhance oil recovery.

延迟成胶弹性硅酸凝胶堵水剂及其性能研究

针对现有硅酸凝胶堵水剂普遍存在成胶时间短、成胶后脆性大的问题,结合L油田油藏条件,通过考察活化剂类型及用量,弹性改善剂类型及用量,以及水玻璃用量对成胶时间和弹性模量的影响,得出了一种延迟成胶弹性硅酸凝胶堵水剂。其配方为:6%水玻璃+0.85%活化剂三元弱酸一铵GL-1+0.1%弹性改善剂正电胶,该配方在油藏温度65℃下,成胶强度达到E级的时间为72 h,成胶后的弹性模量为589.46 Pa。采用填砂管实验评价了堵水剂的注入性及封堵性,结果表明堵水剂在L油田中具有良好的注入性及封堵性,在渗透率为1168.06×10^(-3)~5061.57×10^(-3)μm^(2)的填砂管中,注入0.8 PV的最高注入压力仅有0.72 MPa,封堵率均>96%。该堵水剂可用于L油田的油井堵水。

Sol-Gel法合成SrO-TiO_2-SiO_2:Eu^(3+),Bi^(3+)发光材料

用Ｓｏｌ－Ｇｅｌ法合成了ＳｒＯ－ＴｉＯ_２－ＳｉＯ_２为基质、稀土Ｅｕ^（３＋）激活的发光材料；研究了材料的合成条件，测试了样品的激发光谱、发射光谱、Ｘ－ｒａｙ衍射光谱等；用ＴＧＡ－ＤＴＡ分析了样品合成时的反应行为；获得了合成样品的最佳组成及最佳实验条件。

Sol-gel工艺制备二氧化硅超微细粉及其机理的研究

本文采用sol-gel工艺制备了二氧化硅超微细粉,SiO_2超微细粉粒度可达30nm左右,呈卵园形.并用FT-IR、XRD、DTA/TG和TEM等手段研究了二氧化硅超微细粉在煅烧过程中的物相和显微结构的变化.结果发现二氧化硅超微细粉的凝胶结构在低于300℃时干燥是稳定的,从低温(100℃)到高温(1500℃)煅烧过程中SiO_2超微细粉均为非晶态.

The Reaction Mechanism between MgO and Microsilica at Room Temperature

It was proved that MgO and MicroSilica can react at room temperature, giving a hardened product primarily comprised of Mg （ OH ）2 and Magnesium Silicate Hydrate （ M- S- H ）. The reaction ratio and process and the chemical composion of M- S- H were studied and analyzed by QXRD and DTA- TG. The experimental results indicate that much Mg（ OH）2 and less M-S-H were formed at early period. After 7 days there is no change in the quantity of Mg（ OH）2, while M-S-H was increased slowly. The chemical composion of M-S-H would vary with the mix proportion in the hydrution process , but M1.32 SH2.37 is finally the approximute form.

Luminescence properties of red-emitting Ca_2Al_2SiO_7:Eu^(3+) nanoparticles prepared by sol-gel method

A series of red-emitting Ca2_xA12SiOT：xEu^3＋ （x = 1 mol.%-10 tool.%） phosphors were synthesized by the sol-gel method. The effects of annealing temperature and doping concentration on the crystal structure and luminescence properties of Ca2A12SiO7：Eu^3＋ phosphors were investigated. X-ray diffraction （XRD） profiles showed that all peaks could be attributed to the tetragonal Ca2A12SiO7 phase when the sample was annealed at 1000℃. Scanning electron microscopy （SEM） micrographs indicate that the phosphors have an irregularly rounded mor- phology with particles of about 200 nm. Excitation spectra showed that the strong broad band at around 258 nm and weak sharp lines in 350-490 nm were attributed to the charge transfer band of Eu^3＋-O^2- and f-f transitions within the 4f^6 configuration of Eu^3＋ ions, respectively. Emission spectra implied that the red luminescence could be attributed to the transitions from the ^5D0 excited level to the 7Fj （J = 0, 1, 2, 3, 4） levels of Eu3＋ions with the main electric dipole transition ^5D0→^7F2 （618 and 620 nm）, and Eu^3＋ ions prefer to occupy a lower symmetry site in the crystal lattice. Moreover, the photoluminescence （PL） intensity was strongly dependent on both the sintering temperature and doping concentration, and the highest PL intensity was observed at an Eu^3＋ concentration x = 7 mol.% after annealing at ll00℃. The obtained Ca2A12SiO7：Eu^＋3＋ phosphor may have potential application for the red lamp phosphor.

Fabrication and Luminescence Properties of Ca_2Gd_8 (SiO_4 )_6O_2:Er^(3+) Phosphors via Sol-Gel Process

Ca2RE8(SiO4)6O2(RE = Y, Gd, La) is a kind of ternary rare-earth-metal silicate with the oxyapatite structure, which was used as host materials for the luminescence of various rare earth and mercury-like ions. Ca2Gd8(SiO4)6O2: Er3 + phosphors were prepared through the sol-gel process. X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicate that the phosphors crystallized completely at 1000℃. SEM study reveals that the average grain size is 400 ~ 1000 nm. In Ca2Gd8 (SiO4)6O2 : Er3+ phosphors, the Er3+ shows its characteristic green emission at 528 nm (2H11/2-4I15/2) and 548 nm (4 S3/2-4 I15/2) upon excitation into 382 nm, with an optimum doping concentration of 5% (mole fraction) of Gd3+ in the host lattices.

Synthesis of Long Afterglow Photoluminescent Materials Sr_2MgSi_2O_7∶Eu^(2+), Dy^(3+) by Sol-Gel Method

Long afterglow photoluminescent materials Sr2MgSi2O7 doped with Eu2+, Dy3+ were prepared by sol-gel method. The synthesized samples were characterized by X-ray diffraction. The excitation spectrum, emission spectrum and long decay curve were measured and analyzed. XRD pattern indicates that phosphor is with Sr2MgSi2O7 crystal structure. The wide range of excitation wavelength indicates that luminescent material can be excited by light from ultraviolet ray to visible light. The main peak of emission spectrum is located at 466 nm. Sample excited by visible light can emit bright blue light, and the afterglow time lasts more than 8 h.

Synthesis of C_3S by Sol-Gel Technique and Its Features

Sol-gel method is a technique to synthesize inorganic materials based on wet-chemical reaction theory. The results have shown that reactants tetraethyl orthosilicate （TEOS） and Ca（NO3）2·4H2O can form sol and gel in solution at 50-60 ℃, and the cosolvents are propyl alcohol （NPA） and H2O, the catalyst is HNO3. This sol-gel is burned for 12 hat 1 350-1 450 ℃ so that the organic matter, free water （moisture） in sol-gel system are removed and a solid reaction has taken place to form the resulting product. The product has been confirmed to be C3S by XRD, SEM and 29Si MAS NMR, as well as free lime content of the product which is less than 0.2% was determined by propanetriol-ethanol-method. The analysis determined by EDXA has indicated that the n（Ca）/n（Si） ratio in corresponding to micro-region is close to theoretical value of 3∶1. This resulting product is C3S with Si sites of Q0 polymerization, and has higher purity and hydraulic activities at earlier age of hydration.

Calcined Clay Pozzolan as an Admixture to Mitigate the Alkali-Silica Reaction in Concrete

Calcined clay pozzolan has been used to replace varying portions of high alkali Portland limestone cement in order to study its effect on the alkali-silica reaction (ASR). Portland limestone cement used for the study had a total Na2Oeq of 4.32. Mortar-bar expansion decreased as pozzolan content in the cement increased. The highest expansion was recorded for reference bars with no pozzolan, reaching a maximum of 0.35% at 42 days whilst the expansion was reduced by between 42.5% and 107.8% at 14 days and between 9.4% and 16.4% at 84 days with increasing calcined clay pozzolan content. Mortar bars with 25% pozzolan were the least expansive recording expansion less than 0.1% at all test ages. X-ray diffractometry of the hydrated blended cement paste powders showed the formation of stable calcium silicates in increasing quantities whilst the presence of expansive alkali-silica gel, responsible for ASR expansion, decreased as pozzolan content increased. The study confirms that calcined clay pozzolan has an influence on ASR in mortar bars and causes a significant reduction in expansion at a replacement level of 25%.

SOL-GEL SYNTHESIS AND LUMINESCENCE OF GREEN LIGHT EMITTING PHOSPHORS ZN_2SIO4/MN^(2+)

Mn^(2+) 做了 Zn_2SiO_4 黄磷被锌来源，的大音阶的第五音胶化方法，和影响综合 Mn^(2+) 掺杂物集中和退火的温度被调查。结果证明那锌硝酸盐与强壮的绿排放紧张基于先锋比乙酸锌好基于的先锋。绿轻排放的紧张在 Mn^(2+) 掺杂物集中在附近是的 254 nmwhen 到达一座山峰 5%( 臼齿的百分比) 。黄磷的结构的细节通过 X 光检查 diffractometry， thermogravimetric 和微分热分析被检验。结果显示他们两个都是菱形的结构，它在 1 000 deg C 附近完全在 700 deg C 和 crystallize 下面仍然保持非结晶。光性质 ofZn_2SiO_4/Mn~(2+ 黄磷被刺激和排放系列描绘。

Improved Ti-containing Mesoporous Silica Catalyst Synthesized by Using Anionic Surfactant as Co-template

Ti-containing mesoporous silica materials(Ti-MSs) with isolated tetrahedrally coordinated Ti species have been widely applied in bulk molecular catalysis. Herein, Ti-MSs were synthesized using anionic surfactant SDS as the co-template. The SDS molecular assembled structures can interact with silica species through the interface hydrogen bonds leading to the formation of mesoporous silica structure with compact Ti-O bonds, lower hydrophilicity and low template cost. The influence of adding SDS as the co-template on the oxidation of styrene with aqueous H_2O_2 as the oxidant was investigated. Ti-MSs using SDS as the co-template showed better catalytic performance as compared with mesoporous titanium silicate synthesized with CTAB serving as the sole template. Moreover, the Ti-MSs synthesized at a Ti/Si ratio of 0.005 demonstrated an optimized performance for styrene oxidation with styrene conversion improved by 14.8%, benzaldehyde selectivity improved by 13.7% and styrene oxide selectivity improved by 9.2% when the reaction time was 6 h.

磷肥工业副产含氟硅胶的综合利用

磷肥工业副产含氟硅胶的资源化利用是磷肥行业亟待解决的问题之一,若不对其回收利用,不仅是一种资源的浪费,还会对环境造成污染。介绍了磷肥工业副产含氟硅胶制备液体硅酸钠、五水偏硅酸钠、层状结晶二硅酸钠、4A分子筛、白炭黑、工业硅、碳化硅、氟硅酸铵和氟化氢铵等资源化利用技术,并就磷肥工业副产含氟硅胶的利用问题提出建议。

硅和锂的物质的量之比对二硅酸锂玻璃陶瓷组织结构和抗弯强度的影响

采用溶胶-凝胶法(sol-gel)和常压烧结工艺制备了用于牙科修复的二硅酸锂玻璃陶瓷(LDGC),研究了原料配比中硅(Si)和锂(Li)的物质的量之比(M)及温度对LDGC物相成分、显微结构和力学性能的影响.结果表明:M越高,煅烧温度越高,越有利于二硅酸锂(Li2Si2O5)相的形成.850℃烧结,M为1.54的LDGC抗弯强度可达168.6 MPa,孔隙率仅为0.3%.同时,也讨论了溶胶-凝胶法制备LDGC相较于传统熔融法的优势与不足,所制备的高强度LDGC在牙科修复领域具有广阔的发展前景.

国内外油田硅酸盐堵剂研究进展

综述了硅酸凝胶体系、硅酸盐沉淀体系、硅酸盐/聚合物复合体系、硅酸盐/表面活性剂复合体系和硅酸凝胶/泡沫复合体系,主要介绍了不同体系堵剂的概念、作用机理、发展现状及发展趋势。