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Sample records for borophosphates

  1. Dynamic and Mechanical Properties of Calcium Borophosphate Glasses in Relation to Structure and Topology

    DEFF Research Database (Denmark)

    Hermansen, Christian; Yue, Yuanzheng

    Calcium borophosphate glasses and glass ceramics are of interest as bone-replacement implants as they can bond to bone through an apatite layer, and dissolve in vitro at a rate comparable to the growth rate of natural bone. We investigate the pseudo-binary join between CaO•P2O5 and CaO•2B2O3...

  2. A Novel Borophosphate Coordination Polymer with Sandwich-type Supramolecular Architecture

    Institute of Scientific and Technical Information of China (English)

    Mao Feng LI; Heng Zhen SHI; Yong Kui SHAN; Ming Yuan HE

    2004-01-01

    A novel borophosphate (Hmel)3{Co2[(mel)2(HPO4)2(PO4)](H3BO3·H2O} (mel = melamine) has been synthesized under mild solvothermal conditions. The structure of the compound exists a high ordered organic-inorganic sandwich-type supramolecular architecture via metal-coordination, hydrogen bonds and π-π stacking interactions.

  3. Spectral studies on CuO in sodium–calcium borophosphate glasses

    Indian Academy of Sciences (India)

    S SHAILAJHA; K GEETHA; P VASANTHARANI

    2016-08-01

    Transparent borophosphate glasses doped with CuO were prepared by melt quenching technique. X-ray diffraction (XRD), optical and luminescence properties of sodium–calcium borophosphate glasses doped with CuO have been studied. The XRD results showed the amorphous nature of the sample. The introduction of CuO was favourable for the colour changes from light blue to dark bluish green colour. Direct optical energy bandgaps before and after doping with different percents of copper oxide obtained in the range 4.81–2.99 eV indicated the role of copper in the glassy matrix by ultraviolet (UV) spectra. The glasses have more than 80% transparency for emission wavelength range, and strong absorption bands due to the charge transition of the Cu$^+$ and Cu$^{2+}$ ions were observed. The emission bands observed in the UV and blue regions are attributed to 3d$^9$4s–3d$^{10}$ triplet transition in Cu$^+$ ion.

  4. Immobilization of gadolinium in iron borophosphate glasses and iron borophosphate based glass-ceramics: Implications for the immobilization of plutonium(Ⅲ)

    Science.gov (United States)

    Wang, Fu; Liao, Qilong; Dai, Yunya; Zhu, Hanzhen

    2016-08-01

    Immobilization of gadolinium (Gd), a nonradioactive surrogate for Pu3+, in iron borophosphate glasses/glass-ceramics (IBP glasses/glass-ceramics) has been investigated. The IBP glass containing 4 mol% Gd2O3 is homogeneously amorphous. At higher Gd2O3 concentrations, additional Gd is retained in the glasses as crystalline inclusions of monazite GdPO4 crystalline phase detected with X-ray diffraction. Moreover, Gd2O3 addition increases the Tg of the IBP glasses in glass formation range, which is consistent with the structural modification of the glasses. The structure of the Gd2O3-loaded IBP glasses/glass-ceramics is mainly based on pyrophosphate units. The chemical durability of Gd2O3-loaded IBP glasses/glass-ceramics is comparable to widely used borosilicate glass waste forms and the existence of monazite GdPO4 crystalline phase does not degrade the aqueous chemical durability of the IBP glasses/glass-ceramics. The Gd-loading results imply that the solubility should not be a limiting factor in processing nuclide Pu3+ if the formed crystalline phase(s) have high chemical durability.

  5. Proprietes optiques non lineaires des verres borophosphates de titane ou de niobium

    OpenAIRE

    Cardinal, Thierry

    1997-01-01

    Les verres présentant des propriétés optiques non linéaires importantes constituent des candidats pour des applications de commutation optique ou de propagation soliton. Les verres du système vitreux (1 - x) (0,05Na2B4O7 - 0,95NaPO3) (x TiO2 ou x Nb2O5) ou l' oxyde de titane ou de niobium, réputés non linéaires, sont introduits en fortes proportions sont élaborés et caractérisés du point de vue optique et thermique. Une étude comparative de ces verres borophosphates de titane ou de niobium av...

  6. New bismuth borophosphate Bi4BPO10: Synthesis, crystal structure, optical and band structure analysis

    International Nuclear Information System (INIS)

    New bismuth borophosphate Bi4BPO10 was obtained by spontaneous crystallization from the melt of correspondent composition at 804 °C. Crystal structure with orthorhombic lattice parameters: a = 22.5731(3) Å, b = 14.0523(2) Å, c = 5.5149(1) Å, V = 1749.34(4), Z = 8, SG Pcab was determined by X-ray powder diffraction technique. The [Bi2O2]2+ -layers, which are typical for bismuth oxide compounds, transform into cationic endless strips of 4 bismuth atoms width directed along the c-axis in Bi4BPO10. The strips combining stacks are separated by flat triangle [BO3]3− -anions within stacks. Neighboring stacks are separated by tetrahedral [PO4]3−-anions and shifted relatively to each other. Bismuth atoms are placed in 5–7 vertex oxygen irregular polyhedra. Bi4BPO10 is stable up to 812 °C, then melts according to the peritectic law. The absorption spectrum in the range 350–700 nm was obtained and the width of the forbidden band was estimated as 3.46 eV. The band electronic structure of Bi4BPO10 was modeled using DFT approach. The calculated band gap (3.56 eV) is in good agreement with the experimentally obtained data. - Graphical abstract: Display Omitted - Highlights: • New bismuth borophosphate with composition Bi4BPO10 was synthesized. • The crystal structure was determined by X-ray powder diffraction technique. • Bismuth-oxygen part [Bi4O3]6+ forms endless strips of 4 bismuth atoms width. • Electronic structure was modeled by DFT method. • The calculated band gap (3.56 eV) is very close to the experimental one (3.46 eV)

  7. Structural and luminescence studies of europium ions in lithium aluminium borophosphate glasses

    Institute of Scientific and Technical Information of China (English)

    Poh Sum Wong; Ming Hua Wan; Rosli Hussin; Hendrik O Lintang; Salasiah Endud

    2014-01-01

    Eu3+doped borophosphate glasses with the chemical composition 20Li2O-30Al2O3-10B2O3-40P2O5-xEu2O3 (where x=0.05 mol.%, 0.1 mol.%, 1.0 mol.%, 1.5 mol.%and 2.0 mol.%) were prepared by conventional melt quenching technique. The structural and luminescence properties of the prepared Eu3+doped borophosphate glasses were studied and compared with reported results. The XRD pattern showed the amorphous nature of the prepared glasses. Whereas, the FTIR spectra revealed the vibrational modes in the prepared glasses. The bonding parameters (βandδ) were calculated through the excitation spectra. Judd-Ofelt (J-O) intensity pa-rameters were calculated from the emission spectra and were used to determine transition probability (A), stimulated emission cross-section (σEP ), radiative lifetime (τR) and branching ratios (βexp) for the transition 5D0→7Fj (j=1, 2, 3 and 4) of Eu3+ ions. Furthermore, the luminescence intensity ratio (R) of 5D0→7F2 to 5D0→7F1 transition was also calculated. Transition 5D0→7F2 had the highest value of stimulated emission cross-section and branching ratios and the results were comparable with the reported values. This indicated that the present glass is promising host material for Eu3+doped fiber amplifiers.

  8. Investigations on optical properties of Sm{sup 3+} ion doped boro-phosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Vijayakumar, R.; Suthanthirakumar, P.; Karthikeyan, P.; Marimuthu, K., E-mail: mari-ram2000@yahoo.com [Department of Physics, Gandhigram Rural Institute – Deemed University, Gandhigram – 624302 (India)

    2015-06-24

    The Sm{sup 3+} doped Boro-phosphate glasses with the chemical composition 60H{sub 3}BO{sub 3}+20Li{sub 2}CO{sub 3}+10ZnO+(10−x) H{sub 6}NO{sub 4}P+xSm{sub 2}O{sub 3} (where x= 0.1, 0.5, 1 and 2 in wt%) have been prepared by melt quenching technique. The prepared glasses were characterized through optical absorption and luminescence spectral measurements. The band gap energies corresponding to the direct and indirect allowed transitions and the Urbach’s energy values were estimated from the absorption spectra. Judd-Ofelt intensity parameters have been derived to predict the radiative properties of the various emission transitions. In order to identify the emission color of the prepared glasses, the emission intensities were analyzed using CIE 1931 color chromaticity diagram. The energy transfer process takes place between Sm{sup 3+}−Sm{sup 3+} ions through cross-relaxation mechanism have also been investigated and the results were discussed and reported.

  9. Intermediate length scale organisation in tin borophosphate glasses: new insights from high field correlation NMR.

    Science.gov (United States)

    Tricot, G; Saitoh, A; Takebe, H

    2015-11-28

    The structure of tin borophosphate glasses, considered for the development of low temperature sealing glasses or anode materials for Li-batteries, has been analysed at the intermediate length scale by a combination of high field standard and advanced 1D/2D nuclear magnetic resonance techniques. The nature and extent of B/P mixing were analysed using the (11)B((31)P) dipolar heteronuclear multiple quantum coherence NMR sequence and the data interpretation allowed (i) detecting the presence and analysing the nature of the B-O-P linkages, (ii) re-interpreting the 1D (31)P spectra and (iii) extracting the proportion of P connected to borate species. Interaction between the different borate species was analysed using the (11)B double quantum-simple quantum experiment to (i) investigate the presence and nature of the B-O-B linkage, (ii) assign the different borate species observed all along the composition line and (iii) monitor the borate network formation. In addition, (119)Sn static NMR was used to investigate the evolution of the chemical environment of the tin polyhedra. Altogether, the set of data allowed determining the structural units constituting the glass network and quantifying the extent of B/P mixing. The structural data were then used to explain the non-linear and unusual evolution of the glass transition temperature.

  10. White light simulation and luminescence studies on Dy{sup 3+} doped Zinc borophosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Vijayakumar, R. [Department of Physics, Gandhigram Rural University, Gandhigram 624302 (India); Venkataiah, G. [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Marimuthu, K., E-mail: mari_ram2000@yahoo.com [Department of Physics, Gandhigram Rural University, Gandhigram 624302 (India)

    2015-01-15

    The Dy{sup 3+} doped Zinc borophosphate glasses with the chemical composition (79-x)B{sub 2}O{sub 3}+xP{sub 2}O{sub 5}+10Li{sub 2}O+10ZnO+1Dy{sub 2}O{sub 3} (where x=0, 10, 20, 30 and 50 in wt%) have been prepared by melt quenching technique. The prepared glass samples were characterized through optical absorption, emission and decay measurements. The bonding parameters, optical band gap and Urbach's energy values were calculated from the optical absorption spectra to explore the bonding nature of the Dy–O metal ligand and electronic band structure of the studied glasses. Judd–Ofelt (JO) intensity parameters were calculated from the absorption spectra by using the JO theory and it gives information about symmetry of the ligand environment around the Dy{sup 3+} ion site. The Y/B intensity ratio and radiative properties were obtained from the emission spectra and the results were compared with the reported literature. The x, y chromaticity color coordinates of the studied glasses were analyzed using a CIE 1931 color chromaticity diagram and found that the x, y coordinates lie in the white light region. The decay curve measurements of the prepared glasses exhibit non-exponential behavior and are well fitted to Inokuti–Hirayama (IH) model to understand the energy transfer mechanism between Dy{sup 3+} ions. The Q, R{sub 0} and C{sub DA} values of the prepared Dy{sup 3+} doped glasses were obtained from the IH model and the results were discussed and compared with the reported literature.

  11. Structural and luminescence properties of Mn2+ ions doped calcium zinc borophosphate glasses

    International Nuclear Information System (INIS)

    Highlights: • FT-IR revealed that the network structures are from borate and phosphate network. • The PL spectrum exhibits a green emission band at 582 nm (4T1g → 6A1g). • As the concentration of Mn2+ ions is increased, the emission band had been red shifted. • These glasses are found to have potential applications as luminescent optical materials. - Abstract: Calcium zinc borophosphate glasses (CaZnBP) doped with various concentrations of Mn2+ ions and borate and phosphate as variable were prepared using conventional melt quenching technique. The structure of obtained glasses were examined by means of use: X-ray diffraction (XRD) and fourier transform infrared (FT-IR). XRD analysis confirmed amorphous nature of glass samples. The FT-IR spectra reveals the presence of both borate and phosphate vibrational modes in the prepared glasses. The doping of Mn2+ ions (2–10 mol%) shows no significant changes in the main IR vibrational bands. Optical properties were studied by measuring the near infrared photoluminescence (PL) spectra. CaZnBP glasses exhibited intense green emission peak (582 nm) (tetrahedral symmetry), which is assigned to a transition from the upper 4T1g → 6A1g ground state of Mn2+ ions. As the concentration of Mn2+ ions increases, the emission band increases from 582 nm to 650 nm and exhibited a red light emission (octahedral symmetry). The decay curves of 4T1g level were examined for all concentrations and the measured lifetimes are found to depend strongly on Mn2+ concentrations. From the emission characteristic parameters of 6A1g (S) level, it shows that the CaZnBP glasses could have potential applications as luminescent optical materials, visible lasers and fluorescent display devices

  12. Structural and luminescence properties of Mn{sup 2+} ions doped calcium zinc borophosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Ming Hua, E-mail: wanminghua819@gmail.com [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Wong, Poh Sum, E-mail: pohsumwong@gmail.com [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Hussin, Rosli, E-mail: roslihussin@utm.my [Phosphor Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Lintang, Hendrik O., E-mail: hendrik@ibnusina.utm.my [Catalytic Science and Technology (CST) Research Group, Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Endud, Salasiah, E-mail: salasiah@kimia.fs.utm.my [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor (Malaysia)

    2014-05-15

    Highlights: • FT-IR revealed that the network structures are from borate and phosphate network. • The PL spectrum exhibits a green emission band at 582 nm ({sup 4}T{sub 1g} → {sup 6}A{sub 1g}). • As the concentration of Mn{sup 2+} ions is increased, the emission band had been red shifted. • These glasses are found to have potential applications as luminescent optical materials. - Abstract: Calcium zinc borophosphate glasses (CaZnBP) doped with various concentrations of Mn{sup 2+} ions and borate and phosphate as variable were prepared using conventional melt quenching technique. The structure of obtained glasses were examined by means of use: X-ray diffraction (XRD) and fourier transform infrared (FT-IR). XRD analysis confirmed amorphous nature of glass samples. The FT-IR spectra reveals the presence of both borate and phosphate vibrational modes in the prepared glasses. The doping of Mn{sup 2+} ions (2–10 mol%) shows no significant changes in the main IR vibrational bands. Optical properties were studied by measuring the near infrared photoluminescence (PL) spectra. CaZnBP glasses exhibited intense green emission peak (582 nm) (tetrahedral symmetry), which is assigned to a transition from the upper {sup 4}T{sub 1g} → {sup 6}A{sub 1g} ground state of Mn{sup 2+} ions. As the concentration of Mn{sup 2+} ions increases, the emission band increases from 582 nm to 650 nm and exhibited a red light emission (octahedral symmetry). The decay curves of {sup 4}T{sub 1g} level were examined for all concentrations and the measured lifetimes are found to depend strongly on Mn{sup 2+} concentrations. From the emission characteristic parameters of {sup 6}A{sub 1g} (S) level, it shows that the CaZnBP glasses could have potential applications as luminescent optical materials, visible lasers and fluorescent display devices.

  13. New bismuth borophosphate Bi{sub 4}BPO{sub 10}: Synthesis, crystal structure, optical and band structure analysis

    Energy Technology Data Exchange (ETDEWEB)

    Babitsky, Nicolay A.; Leshok, Darya Y.; Mikhaleva, Natalia S. [Siberian Federal University, 79 Svobodny Av, Krasnoyarsk, 660041 (Russian Federation); Kuzubov, Aleksandr A., E-mail: alexkuzubov@gmail.com [Siberian Federal University, 79 Svobodny Av, Krasnoyarsk, 660041 (Russian Federation); Institute of Physics SB RAS, Krasnoyarsk 660036 (Russian Federation); Zhereb, Vladimir P. [Siberian Federal University, 79 Svobodny Av, Krasnoyarsk, 660041 (Russian Federation); Kirik, Sergei D., E-mail: kiriksd@yandex.ru [Siberian Federal University, 79 Svobodny Av, Krasnoyarsk, 660041 (Russian Federation)

    2015-08-01

    New bismuth borophosphate Bi{sub 4}BPO{sub 10} was obtained by spontaneous crystallization from the melt of correspondent composition at 804 °C. Crystal structure with orthorhombic lattice parameters: a = 22.5731(3) Å, b = 14.0523(2) Å, c = 5.5149(1) Å, V = 1749.34(4), Z = 8, SG Pcab was determined by X-ray powder diffraction technique. The [Bi{sub 2}O{sub 2}]{sup 2+} -layers, which are typical for bismuth oxide compounds, transform into cationic endless strips of 4 bismuth atoms width directed along the c-axis in Bi{sub 4}BPO{sub 10}. The strips combining stacks are separated by flat triangle [BO{sub 3}]{sup 3−} -anions within stacks. Neighboring stacks are separated by tetrahedral [PO{sub 4}]{sup 3−}-anions and shifted relatively to each other. Bismuth atoms are placed in 5–7 vertex oxygen irregular polyhedra. Bi{sub 4}BPO{sub 10} is stable up to 812 °C, then melts according to the peritectic law. The absorption spectrum in the range 350–700 nm was obtained and the width of the forbidden band was estimated as 3.46 eV. The band electronic structure of Bi{sub 4}BPO{sub 10} was modeled using DFT approach. The calculated band gap (3.56 eV) is in good agreement with the experimentally obtained data. - Graphical abstract: Display Omitted - Highlights: • New bismuth borophosphate with composition Bi{sub 4}BPO{sub 10} was synthesized. • The crystal structure was determined by X-ray powder diffraction technique. • Bismuth-oxygen part [Bi{sub 4}O{sub 3}]{sup 6+} forms endless strips of 4 bismuth atoms width. • Electronic structure was modeled by DFT method. • The calculated band gap (3.56 eV) is very close to the experimental one (3.46 eV)

  14. Positive and Negative Mixed Glass Former Effects in Sodium Borosilicate and Borophosphate Glasses Studied by (23)Na NMR.

    Science.gov (United States)

    Storek, Michael; Adjei-Acheamfour, Mischa; Christensen, Randilynn; Martin, Steve W; Böhmer, Roland

    2016-05-19

    Glasses with varying compositions of constituent network formers but constant mobile ion content can display minima or maxima in their ion transport which are known as the negative or the positive mixed glass former effect, MGFE, respectively. Various nuclear magnetic resonance (NMR) techniques are used to probe the ion hopping dynamics via the (23)Na nucleus on the microscopic level, and the results are compared with those from conductivity spectroscopy, which are more sensitive to the macroscopic charge carrier mobility. In this way, the current work examines two series of sodium borosilicate and sodium borophosphate glasses that display positive and negative MGFEs, respectively, in the composition dependence of their Na(+) ion conductivities at intermediate compositions of boron oxide substitution for silicon oxide and phosphorus oxide, respectively. A coherent theoretical analysis is performed for these glasses which jointly captures the results from measurements of spin relaxation and central-transition line shapes. On this basis and including new information from (11)B magic-angle spinning NMR regarding the speciation in the sodium borosilicate glasses, a comparison is carried out with predictions from theoretical approaches, notably from the network unit trap model. This comparison yields detailed insights into how a variation of the boron oxide content and thus of either the population of silicon or phosphorus containing network-forming units with different charge-trapping capabilities leads to nonlinear changes of the microscopic transport properties. PMID:27092392

  15. Low-temperature flux syntheses and characterizations of two 1-D anhydrous borophosphates: Na 3B 6PO 13 and Na 3BP 2O 8

    Science.gov (United States)

    Xiong, Ding-Bang; Chen, Hao-Hong; Yang, Xin-Xin; Zhao, Jing-Tai

    2007-01-01

    Two new anhydrous sodium borophosphates with one-dimensional structure, Na 3B 6PO 13(1) and Na 3BP 2O 8(2), were synthesized by low-temperature molten salts techniques using boric acid and sodium dihydrogen phosphate as flux, respectively. The crystal structures were solved by means of single-crystal X-ray diffraction ( 1, orthorhombic, Pnma (no. 62), a=9.3727(4) Å, b=16.2307(7) Å, c=6.7232(3) Å, Z=4; 2 , monoclinic, C2/ c (no. 15), a=12.567(4) Å, b=10.290(3) Å, c=10.210(3) Å, β=92.492(5)°, Z=8). Compound 1 is characterized by an infinite chain of ∞1{[BPO]} containing eight-membered rings in which all vertexes of borate groups contribute to interconnection. Compound 2 reveals an infinite straight chain ∞1{[BPO]} built of vertex-sharing four-membered rings, and chains in neighboring layers arranged along different orientations. The relations between structures and the synthetic conditions with only traced water are discussed.

  16. Study on the water durability of zinc boro-phosphate glasses doped with MgO, Fe2O3, and TiO2

    Science.gov (United States)

    Hwang, Moon Kyung; Ryu, Bong Ki

    2016-07-01

    The water durability of zinc boro-phosphate (PZB) glasses with the composition 60P2O5-20ZnO-20B2O3- xMeO ( x = 0, 2, 4, 6 and MeO = MgO, Fe2O3, or TiO2) (mol%) was measured, and PZB glass was studied in terms of its thermal properties, density, and FTIR characteristics. The surface conditions and corrosion byproducts were analyzed using scanning electron microscopy. When MgO, Fe2O3, and TiO2 were doped into the PZB glass, Q2 was decreased and Q1 was increased in the phosphate structure, while the number of BO4 structures increased with increasing MeO content. The density of the PZB glass was increased by the addition of Fe2O3 and TiO2, while the glass transition temperature ( T g ) and dilatometric softening temperature ( T d ) were increased when additional MgO, Fe2O3, and TiO2 were added. From the weight loss analysis (95 ◦ C, 96 h), TiO2 doped glass showed the lowest weight loss (1.70 × 10 -3 g/cm2) while MgO doped glass showed the highest value (2.44 × 10 -3 g/cm2), compared with PZB glass (3.07 × 10 -3 g/cm2). These results were discussed in terms of the Me n+ ions in the glass structure, and their different coordination numbers and bonding strengths.

  17. 过渡金属和主族元素硼磷酸盐体系的研究%Investigations on Transition-metal and Main-group-element Borophosphate Systems

    Institute of Scientific and Technical Information of China (English)

    宓锦校; 黄雅熙; 赵景泰; 毛少瑜; 李满荣

    2001-01-01

    总结了作者近几年在硼磷酸盐研究中所合成和表征的10多个新化合物,即元素周期表第4周期从Cr至Ga的元素或氧化物与工业催化剂材料BPO.在高温固相反应中,分别合成出具有3种结构类型的新化合物:新结构类型的三方Cr2[BP3O12]、正交AlPO4型的(B,M)[PO4](M=Mn,Fe.Co,Ni,Cu,Zn)和新型四方(Ga,B)PO4;用水热法合成出NaGa[BP2O7(OH)3]、Na2In2[PO3(OH)]4·H2O和Na4Co3H2(PO4)4·8H2O等新化合物.同时还讨论了硼磷酸盐化合物研究的最新进展及结构化学的一般规律.%Borophosphates have attracted much attention of scientists in the last few years due to the potential applications of these compounds as functional materials. More than ten new compounds in the related systems have been synthesized and characterized here by either solid state reactions or hydrothermal methods. The new compounds have either new structure types like Cr2BP3O12 which contains new building motif, or with very well known structure type like low cristobalite. The general structural features of these compounds have been discussed together with the literature data, and the new developments of the borophosphate research have also been reviewed here.

  18. Investigations of structure and transport in lithium and silver borophosphate glasses

    Science.gov (United States)

    Kumar, Sundeep; Vinatier, Philippe; Levasseur, Alain; Rao, K. J.

    2004-04-01

    Glasses in the system xLi 2O·(1- x)[0.5B 2O 3·0.5P 2O 5] and xAg 2O·(1- x)[0.5B 2O 3·0.5P 2O 5] have been prepared from melt quenching method. Glasses have been characterized for their densities, molar volumes, glass transition temperatures and heat capacities. Structural studies have been done using infrared and high resolution magic angle spinning nuclear magnetic resonance (HR MAS NMR) of 31P, 11B and 7Li nuclei. Boron is present only in tetrahedral coordination except in Li 2O-rich glasses. Transport properties have been investigated over a wide range of frequency and temperature. Silver containing glasses are found to possess higher conductivities and lower barriers than lithium containing glasses. A structural model has been proposed in which pure B 2O 3-P 2O 5 compositions are assumed to be constituted of BPO 4 units and modification occurs selectively on the phosphate moiety. Tetrahedral boron units are thus expected to be retained in the glass structure.

  19. Crystallization of cerium containing iron borophosphate glasses/glass-ceramics and their spectral properties

    Science.gov (United States)

    Wang, Fu; Liao, Qilong; Zhu, Hanzhen; Dai, Yunya; Wang, Hong

    2016-04-01

    The crystallization behaviors of CeO2 containing 36Fe2O3-10B2O3-54P2O5 glasses/glass-ceramics (IBP glasses/glass-ceramics) and the effect of CeO2 addition on the structure of the IBP glasses/glass-ceramics annealed at 850 °C for 10 h were investigated by XRD, SEM and FTIR. The results show that Fe4(PO4)2O and Fe2(PO4)O phases are detected in the IBP glasses/glass-ceramics annealed at 650 °C for 10 h, and traces of FePO4 crystal is also detected when the CePO4 crystallite pre-exists in the unannealed IBP glass-ceramics. When the glasses/glass-ceramics are heat-treated at 850 °C for 10 h, Fe4(PO4)2O, Fe2(PO4)O and a small amount of FePO4 phase are detected. Meanwhile, CePO4 phase also appears in the crystallized IBP glasses/glass-ceramics containing more than 6 mol% (including 6 mol%) CeO2. Moreover, the main structural units of the crystallized glasses/glass-ceramics are [PO4] and [BO4] tetrahedron. [CeO4] tetrahedron also exists in the structure of the crystallized IBP glasses/glass-ceramics containing CeO2. CeO2 addition and the pre-existing CePO4 crystallite improve the resistance of the IBP glasses/glass-ceramics to crystallization, which makes the infrared bands associated with the vibration of [PO4] group increase in intensity and shift to high wave number.

  20. Surface degradation behaviour of sodium borophosphate glass in aqueous media: Some studies

    Indian Academy of Sciences (India)

    K V Shah; M Goswami; S Manikandan; V K Shrikhande; G P Kothiyal

    2009-06-01

    The degradation behaviour of phosphate glass with nominal composition, 40Na2O–10BaO–B2O3–(50–)P2O5, where 0 ≤ ≤ 20 mol%, was studied in water, HCl and NaOH solutions at room temperature to 60°C for different periods extending up to 300 h. These glasses were synthesized by conventional melt-quench technique. Dissolution rates were found to increase with B2O3 content in the glass. The dissolution rates for the glass having 10 mol% B2O3 were found to be 0.002 g/cm2 and 0.015 g/cm2 in distilled water and 5% NaOH solution, respectively, at room temperature after 225 h of total immersion period, whereas it increased considerably to 0.32 g/cm2 in 5% NaOH at 60°C after 225 h. However, glass samples with = 15 and 20 mol% B2O3 were dissolved in 5% HCl solution after 5 h immersion. The degradation behaviour has been correlated with the structural features present in the glass. The optical microscopy of the corroded surface revealed that the corrosion mechanism were different in acid and alkali media.

  1. An optical and structural investigation into CdTe nanocrystals embedded into the tellurium lithium borophosphate glass matrix

    Institute of Scientific and Technical Information of China (English)

    WAGEH; S

    2010-01-01

    Cadmium telluride nanocrystals that form in the TeO2-Li2O-B2O3-P2O5 glass matrix have been synthesized and studied.They are investigated by X-ray diffraction(XRD),optical transmission and infrared spectroscopy.It has been shown that the long annealing time effect on present samples leads to the growth of CdTe nanoparticles and an increase of tellurium oxide on the surface of nanocrystallites.On the other hand,the infrared spectroscopy shows that the phosphate and borate networks of the glass matrices are modified with doping by CdTe nanoparticles.

  2. A comparative study on the sintering behaviour and phase emergence of calcium borophosphate and calcium titanophosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Arvind, A; Dixit, Anupam; Shrikhande, V K; Kothiyal, G P, E-mail: gpkoth@barc.gov.in [Technical Physics and Prototype Engineering Division, Bhabha Atomic Research Centre, Mumbai-400085 (India)

    2009-07-15

    Calcium-phosphate (CaP) based glasses of composition 60CaO-30P{sub 2}O{sub 5}-10B{sub 2}O{sub 3} (CaPB) and 60CaO-30P{sub 2}O{sub 5}-10TiO{sub 2} (CaPT) with high Ca/P ratio (>1.0) were prepared by quenching the melt into water. The glass frit was crystallized at temperatures in the range of 650-850deg. C and XRD revealed that at 650deg. C, the first phase to form was tetragonal {beta}-Ca{sub 2}P{sub 2}O{sub 7} followed by monoclinic {alpha}-Ca{sub 2}P{sub 2}O{sub 7} at 680deg. C. The addition of TiO{sub 2} or B{sub 2}O{sub 3} did not greatly alter the phase emergence. At the same time, when glass pellets were sintered at 600deg. C, for 2-8 hr, the B{sub 2}O{sub 3} containing samples showed better densification than the TiO{sub 2} containing samples. Incorporation of B{sub 2}O{sub 3} lowers the liquidus temperature and greatly reduces the crystallization tendency. This allows for liquid phase sintering leading to higher densification.

  3. A comparative study on the sintering behaviour and phase emergence of calcium borophosphate and calcium titanophosphate glasses

    International Nuclear Information System (INIS)

    Calcium-phosphate (CaP) based glasses of composition 60CaO-30P2O5-10B2O3 (CaPB) and 60CaO-30P2O5-10TiO2 (CaPT) with high Ca/P ratio (>1.0) were prepared by quenching the melt into water. The glass frit was crystallized at temperatures in the range of 650-850deg. C and XRD revealed that at 650deg. C, the first phase to form was tetragonal β-Ca2P2O7 followed by monoclinic α-Ca2P2O7 at 680deg. C. The addition of TiO2 or B2O3 did not greatly alter the phase emergence. At the same time, when glass pellets were sintered at 600deg. C, for 2-8 hr, the B2O3 containing samples showed better densification than the TiO2 containing samples. Incorporation of B2O3 lowers the liquidus temperature and greatly reduces the crystallization tendency. This allows for liquid phase sintering leading to higher densification.

  4. The structural properties of CdO-Bi 2 O 3 borophosphate glass system containing Fe 2 O 3 and its role in attenuating neutrons and gamma rays

    Science.gov (United States)

    Saudi, H. A.; Mostafa, A. G.; Sheta, N.; El Kameesy, S. U.; Sallam, H. A.

    2011-11-01

    A glass system with chemical formula xBi 2O 3-(30- x)CdO-10B 2O 3-20Fe 2O 3-40P 2O 5 (0≤ x≤30) wt% is prepared to be used as radiation shield. The mass attenuation coefficient and half value layer of the glass system to gamma rays have been measured experimentally and compared with those determined from theoretical calculations using the mixture rule of WinXCom program. A database of effective mass removal cross-sections for fast neutrons is also introduced in this work. The obtained results of this study are correlated to the structural properties of these glasses obtained from their IR spectra and the influence of gamma and neutrons irradiation on these structural properties.

  5. Investigation on Structures and Properties of Yb3+-Doped Laser Glasses

    Institute of Scientific and Technical Information of China (English)

    Liu Shujiang; Lu Anxian; Tang Xiaodong; He Shaobo

    2006-01-01

    The Yb3+-doped silicate, phosphate and borophosphate laser glasses were prepared by means of conventional melt quenching technology.The physical and spectral properties of the glasses were investigated.The results show that, due to the existence of OH-, the fluorescence lifetime of phosphate glass is shorter than that of silicate glass, so silicate glass has better spectral properties than phosphate glass.Silicate glass has better mechanical and thermal properties than phosphate glass, but with the addition of B2O3, mechanical and thermal properties of phosphate glass are improved greatly without fluorescence quenching effect.This kind of borophosphate glass can be used in high average power solid state lasers.

  6. A New Ceramic Substrate Glaze with High Resistance to Molten Aluminum

    Institute of Scientific and Technical Information of China (English)

    Ming ZHOU; Ke LI; Da SHU; Jiao ZHANG; Baode SUN; Jun WANG

    2003-01-01

    Corrosion resistance of ceramic substrate glazes to molten aluminum was studied in this paper. The glazes can spreadslightly in aluminum alloy according to SEM examination of solidified interface between the glazes and aluminumalloy. The components of B2O3-P2O5 glazes were not detected with electron probe at the side of aluminum alloynear the interface, but the components of boron-free glaze were detected. It is shown that borophosphate glazes canresist the corrosion of molten aluminum.

  7. Effect of zinc borate on the thermal degradation of ammonium polyphosphate

    International Nuclear Information System (INIS)

    The thermal behaviour of a mixture containing an ammonium polyphosphate based compound (AP760) and zinc borate (ZB) is investigated. After an investigation of the degradation of the pure components, the interactions between them are examined by thermogravimetry. Then, X-ray diffraction (XRD) and 11B and 31P solid-state nuclear magnetic resonance (NMR) measurements have been carried out on residues of mixtures of AP760 and FBZB heat treated at different characteristic temperatures. It reveals the nature of the interactions taking place between the two components. It is demonstrated that reactions lead to the formation of zinc phosphate and of borophosphates. Mechanisms of thermal degradation are proposed

  8. MPS/CAS Cooperation on Solid State Chemistry

    Institute of Scientific and Technical Information of China (English)

    Zhao Jingtai; Rüdiger Kniep

    2004-01-01

    @@ The cooperation between Zhao Jingtai and the Max Planck Institute for Chemical Physics of Solids was initiated immediately after the research field Inorganic Chemistry (headed by Rüdiger Kniep) started its work in Dresden. The first contact was established when Zhao Jingtai came from the Xiamen University as a Max Planck fellow. At that time, the chemistry of the intermetallic compounds of rare-earth metals was chosen as a topic of joint investigations with Yuri Grin. Later, the solid state chemistry of the borophosphates was added to the program of concerted research in the group of Zhao Jingtai and the Max Planck Institute for Chemical Physics of Solids.

  9. Na2O.B2O3-Al2O3-P2O5 system as a medium for vitrification of nuclear power plant wastes

    International Nuclear Information System (INIS)

    Laboratory experiments have shown that in the studied system 3Na2O.B2O3-Al2O3-P2O5 in the area of the delineated simplex triangle it is possible to obtain glasses which are very easily melted at temperatures of approximately 1100 degC. These glasses have only a slight tendency to crystallization and a high dilatability, especially in the region of transformation. Also studied was the hydrolytical and chemical resistance of different glass samples. The pilot plant experiment verified the possibility of the fixation of radioactive wastes in material based on sodium borophosphates. (J.B.)

  10. Ion transport studies on Li2O-PbO-B2O3-P2O5 glass system

    Science.gov (United States)

    Muralidhara, R. S.; Anavekar, R. V.

    2009-07-01

    Electrical conductivity of Li+ ion conducting borophosphate glass system with the general formula xLi2O -10PbO-(90-x) [55B2O3 + 45 P2O5] where x=20, 25, 30 and 35 has been carried out both as a function of temperature and frequency in the temperature range 303K to 503K and over frequencies 20 Hz to 12 MHz. The dc conductivities show Arrhenius behaviour while exhibiting composition dependence. Edc estimated from Arrhenius plots varies from 0.82 eV 0.88 eV. The ac conductivity behaviour has been analyzed using a single power law. The exponent `s' obtained from the power law fits is found to have values ranging from 0.45 to 0.84.in these glasses and shows moderate temperature dependence The stretched exponent β also is seen to vary slightly with temperature. Scaling behaviour also has been carried out using the reduced plots of conductivity and frequency. The time-temperature superposition of data points is found to be satisfactory indicating that the ion transport mechanism remains the same in the entire range of temperatures and compositions studied. The results have been explained considering the borophosphate network and the role of Li2O as a glass modifier.

  11. Influence of addition of B2O3 on properties of Yb3+ -doped phosphate laser glass

    Institute of Scientific and Technical Information of China (English)

    LIU Shu-jiang; LU An-xian; TANG Xiao-dong; HE Shao-bo

    2006-01-01

    The three host glasses doped with Yb3+ were prepared by means of conventional melt quenching technol ogy, and the influence on physical and spectral properties of phosphate glass due to addition of B2O3 was investigated and compared with silicate glass. The results show that due to the existence of OH- impurities which induce thenon-radiative route, the fluorescence lifetime of phosphate glass is shorter, so silicate glass has better spectral properties than phosphate glass. Silicate glass has more excellent thermal-mechanical properties than phosphate glass,but with the addition of B2O3, thermal-mechanical properties of phosphate glass are improved greatly without fluo rescence quenching effect, and this kind of borophosphate glass will be the candidate to be used in high average pow er solid state laser.

  12. Zero photoelastic and water durable ZnO–SnO–P2O5–B2O3 glasses

    International Nuclear Information System (INIS)

    We report properties of zero birefringent xZnO–(67–x)SnO–(33–y)P2O5–y B2O3 glasses, within 18.5 ≤ x ≤ 22 and y = 0, 3, and 10 mol. %. These compositions of boro-phosphate glasses provide both zero photoelastic constant (PEC) and improved water durability. x = 19 and y = 3 compositions show minimum PEC of −0.002 × 10−12 Pa−1, which can contribute to candidate material for fiber current sensor devise without lead. The structures of zero photoelastic glasses were investigated by Raman scattering and nuclear magnetic resonance spectroscopies. Compositions of zero PEC glasses are explained by the empirical model proposed by Zwanziger et al. [Chem. Mater. 19, 286-290 (2007)

  13. Electrochemical mechanisms in tin-containing composite materials for negative electrodes in Li-ion batteries: Transformation of the interfacial tin species during the first galvanostatic discharge of Sn[BPO 4] 0.4

    Science.gov (United States)

    Conte, Donato E.; Stievano, Lorenzo; Olivier-Fourcade, Josette; Jumas, Jean-Claude; Willmann, Patrick

    The Sn[BPO 4] 0.4 composite material is composed of three main constituents: the electrochemically active Sn 0 species, the BPO 4 buffer matrix, and an interfacial amorphous Sn II borophosphate phase which acts as a link between the other two, improving the cohesion of the whole composite. In this paper, we report an investigation of the effect of the reaction time on structure and size of this interfacial layer formed between the Sn 0 and the BPO 4 particles. 119Sn Mössbauer spectroscopy shows an increase in the amount of the oxidized Sn II species with the increase of the reaction time following a quasi-kinetic profile. Operando Mössbauer spectroscopy allowed the study of the transformation of the interface at the beginning of the first electrochemical cycle, indicating that the big irreversible loss during the first discharge is closely related to the increase of the amount of Sn II in the amorphous interface.

  14. Effect of B2O3 addition on microhardness and structural features of 40Na2O–10BaO–B2O3–(50–)P2O5 glass system

    Indian Academy of Sciences (India)

    K V Shah; M Goswami; M N Deo; A Sarkar; S Manikandan; V K Shrikhande; G P Kothiyal

    2006-02-01

    Phosphate glasses having composition, 40Na2O–10BaO–B2O3–(50–)P2O5, where = 0–20 mol% were prepared using conventional melt quench technique. Density of these glasses was measured using Archimedes principle. Microhardness (MH) was measured by Vicker’s indentation technique. Structural studies were carried out using IR spectroscopy and 31P and 11B MAS NMR. Density was found to vary between 2.62 and 2.77 g/cc. MH was found to increase with the increase in boron content. 31P MAS NMR spectra showed the presence of middle 2 groups and end 1 and 0 groups with P–O–B linkages. FTIR studies showed the presence of BO3 and BO4 structural units along with the depolymerization of phosphate chains in conformity with 31P MAS NMR. 11B NMR spectra showed increase in BO4 structural units with increasing boron content. The increase in MH with B2O3 content is due to the increase of P–O–B linkages and BO4 structural units as observed from MAS NMR studies resulting in a more rigid borophosphate glass networks.

  15. Flame retardancy mechanisms of bisphenol A bis(diphenyl phosphate) in combination with zinc borate in bisphenol A polycarbonate/acrylonitrile-butadiene-styrene blends

    International Nuclear Information System (INIS)

    Bisphenol A polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) with and without bisphenol A bis(diphenyl phosphate) (BDP) and 5 wt.% zinc borate (Znb) were investigated. The pyrolysis was studied by thermogravimetry (TG), TG-FTIR and NMR, the fire behaviour with a cone calorimeter applying different heat fluxes, LOI and UL 94. Fire residues were examined with NMR. BDP affects the decomposition of PC/ABS and acts as a flame retardant in the gas and condensed phases. The addition of Znb results in an additional hydrolysis of PC. The fire behaviour is similar to PC/ABS, aside from a slightly increased LOI and a reduced peak heat release rate, both caused by borates improving the barrier properties of the char. In PC/ABS + BDP + Znb, the addition of Znb yields a borate network and amorphous phosphates. Znb also reacts with BDP to form alpha-zinc phosphate and borophosphates that suppress the original flame retardancy mechanisms of BDP. The inorganic-organic residue formed provides more effective flame retardancy, in particular at low irradiation in the cone calorimeter, and a clear synergy in LOI, whereas for more developed fires BDP + Znb become less effective than BDP in PC/ABS with respect to the total heat evolved.

  16. Strain engineering of nonlinear boron phosphate for phase matching in the ultraviolet region: a first-principles study

    Science.gov (United States)

    Hu, Jinyu; Ma, Zuju; Li, Jun; He, Chao; Li, Qiaohong; Wu, Kechen

    2016-05-01

    Borophosphates, particularly BPO4 (BPO) crystals, have attracted attention in laser frequency conversion devices because of their short ultraviolet cutoff edge and relatively large second harmonic generation (SHG) response, which is almost twice as great as that of KH2PO4. However, the birefringence of BPO (approximately 0.005) is too small to satisfy the phase matching condition in the ultraviolet spectral region, restricting the laser output efficiency. Here we systematically examine the influence of mechanical strains on the atomic structure as well as the electronic and optical properties of BPO using first-principles calculations. Interestingly, we find that the birefringence of BPO can be enhanced by ~0.06 through external uniaxial strain along the c-axis. Meanwhile, compressive strain can increase the band gap and SHG coefficients effectively. Refractive-index dispersion is also emphasized in this work. Our results indicate that phase matching in the ultraviolet region (266 nm) can be achieved under  -10% strain (3.9 GPa). This investigation is helpful for understanding the structure-property relationship of BPO under strain, and it also indicates its possible use as a promising ultraviolet nonlinear optical crystal.

  17. Sn-0.4BPO 4 composite as a promising negative electrode for rechargeable lithium batteries

    Science.gov (United States)

    Aboulaich, Abdelmaula; Womes, Manfred; Olivier-Fourcade, Josette; Willmann, Patrick; Jumas, Jean-Claude

    2010-01-01

    The structural and textural properties of a Sn-0.4BPO 4 composite material synthesized by ex situ dispersion of β-Sn in a BPO 4 matrix were investigated by using several complementary techniques to study the global order (XRD, TGA-DSC, SEM-XEDS) and the local order (FT-IR, 119Sn Mössbauer spectroscopy and X-ray absorption spectroscopy). The results reveal that the composite material consists of three main components: an electrochemically active species "Sn", an inactive matrix "BPO 4", and an amorphous Sn(II) borophosphate which acts as a link between the two former and which improves the cohesion of the composite. The electrochemical performances of the composite material were tested in Swagelok-type cells with metallic Li as counter-electrode. It shows a high reversible capacity of about 500 mAh g -1 at a C/20 rate, and a very good stability under cycling even at very fast rates of C or C/1.3.

  18. Investigation of crystal structure and associated electronic structure of Sr 6BP 5O 20

    Science.gov (United States)

    Ehrenberg, Helmut; Laubach, Sonja; Schmidt, P. C.; McSweeney, R.; Knapp, M.; Mishra, K. C.

    2006-04-01

    Strontium borophosphate phosphate (Sr 6BP 5O 20, SrBP), activated by divalent europium ions is a bluish-green phosphor emitting in a broad band with the emission peak near 480 nm. In this paper, we report the crystal structure of SrBP determined from an analysis of the X-ray diffraction pattern of a prismatic single crystal (size 60 μm×50 μm×40 μm). This crystal was chosen from undoped phosphor powder samples prepared for this purpose by solid-state reaction. SrBP is observed to crystallize in a body-centered tetragonal lattice with the lattice parameters a=9.7895(7) Å and c=19.032(3) Å, the associated space group being I4¯c2 (space group 120). Using the structural data from this study, we have also calculated its electronic structure using the augmented spherical wave method and the local density approximation (LDA). We show the ordering of the electronic states by the density of states (DOS) and the partial DOS plots. The LDA gives a direct optical band gap at the Γ point of about 5 eV. The significance of the crystal structure and associated electronic structure is discussed with respect to maintenance of this phosphor in Hg-discharge lamps.

  19. Synthesis, thermal and photoluminescent properties of ZnSe- based oxyfluoride glasses doped with samarium

    International Nuclear Information System (INIS)

    Rare earth (RE) doped glasses and glass ceramic materials have recently received considerable attention because of their potential or realized applications as X-ray intensifying screens, phosphors, detectors, waveguides, lasers etc. [1]. In this work, we present a new RE doped ZnO-ZnSe-SrF2-P2O5-B2O3-Sm2O3-SmF3 (ZSPB) glass system synthesized by melt quenching technique. The resulting glasses were visually fully transparent and stable with glass the transition temperatures around 530°C. The thermal properties of this glass system were characterized by Modulated Differential Scanning Calorimetry (MDSC) measurements before and after annealing at 650°C. We have characterized these glasses by Raman spectroscopy and photoluminescence (PL) measurements over the UV-VIS range using light emitting diodes (LED) and laser diodes (LD) excitation sources. We have also irradiated thermally treated and non-treated glass samples by X-rays and have studied the resulting PL. We discuss the results in terms of previously reported models for Sm-doped Zn-borophosphate oxide, oxyfluoride and oxyselenide glasses

  20. Crystal structure of ABPO5 and optical study of Pr3+ embedded in these compounds

    Science.gov (United States)

    Ben Ali, A.; Antic-Fidancev, E.; Viana, B.; Aschehoug, P.; Taibi, M.; Aride, J.; Boukhari, A.

    2001-10-01

    The crystal structure of borophosphates ABPO5 (A = alkaline earth or Pb) was resolved on a polycrystalline sample using the Rietveld method. The x-ray diffraction patterns data show that ABPO5 crystallize in a centrosymmetric space group P3121 and their structure is related to the borogermanates REBGeO5 with a stillwellite-type structure. Pr3+ ion was used as a local structural probe to corroborate the structural resolution results. Absorption and fluorescence spectra of A1-xPrxBP1-xGexO5 (A = alkaline earth or Pb; x = 0.05) have been investigated at different temperatures. At 9 K the 3H4 → 3P0 transition of trivalent praseodymium ion (4f2 configuration) is observed as a single line. This indicates a unique crystallographic site for the rare earth ion in these compounds replacing the divalent cation. Energy level schemes were deduced from the low-temperature spectroscopic measurements. Comparing the electronic level splittings of studied compounds with the already reported data on REBGeO5 doped with Pr3+ ion, it is possible to dispel the doubt existing about structural determination. Moreover, under 460 nm excitation, intense red emission of trivalent praseodymium is observed corresponding to 1D2 → 3H4 transition. The lifetime measurements of 1D2 level have been performed for all the title compounds.

  1. Interfacial antiwear and physicochemical properties of alkylborate-dithiophosphates.

    Science.gov (United States)

    Shah, Faiz Ullah; Glavatskih, Sergei; Höglund, Erik; Lindberg, Mats; Antzutkin, Oleg N

    2011-04-01

    Boron compounds have become of interest in tribology because of their unique tribochemical and tribological properties. At the same time, dialkyldithiophosphates (DTPs) of transition metals have been extensively used as multifunctional additives in lubricants to control friction and reduce wear in mechanical systems. Because of the environmental pollution and health hazards of these compounds, ashless compounds with reduced amounts of sulfur and phosphorus are desirable. This work reports on the synthesis, characterization, and tribological properties of a new class of compounds, alkylborate-dithiophosphates. This class combines two high-iron-affinity surface active groups, borate and dialkyldithiophosphate, into a single molecule. The final products, viscous liquids, were characterized by FT-IR, multinuclear (1)H, (13)C, (31)P, and (11)B NMR spectroscopy and thermal analyses. Residues of one representative compound from this class, DPB-EDTP, after thermal analyses were additionally characterized by multinuclear (13)C, (31)P and (11)B MAS and (31)P CP/MAS NMR spectroscopy. Solid-state NMR data suggest that a dominant part of the solid residue of DPB-EDTP consists of borophosphates. Antiwear and friction properties of a mineral oil with these novel additives were evaluated in a four-ball tribometer in comparison with O,O'-di-n-butyl-dithiophosphato-zinc(II), Zn-BuDTP, as a reference lubricant additive. The surface morphology and the elemental composition of the tribofilms were characterized using scanning electron microscopy with energy-dispersive X-rays spectroscopy (SEM/EDS). The results show that alkylborate-dithiophosphates, with substantially reduced amounts of sulfur and phosphorus compared with Zn-BuDTP, have considerably better antiwear and friction performance. PMID:21381776

  2. Sn x[BPO 4] 1-x composites as negative electrodes for lithium ion cells: Comparison with amorphous SnB 0.6P 0.4O 2.9 and effect of composition

    Science.gov (United States)

    Conte, Donato Ercole; Aboulaich, Abdelmaula; Robert, Florent; Olivier-Fourcade, Josette; Jumas, Jean-Claude; Jordy, Christian; Willmann, Patrick

    2010-01-01

    A comparative study of two Sn-based composite materials as negative electrode for Li-ion accumulators is presented. The former SnB 0.6P 0.4O 2.9 obtained by in-situ dispersion of SnO in an oxide matrix is shown to be an amorphous tin composite oxide (ATCO). The latter Sn 0.72[BPO 4] 0.28 obtained by ex-situ dispersion of Sn in a borophosphate matrix consists of Sn particles embedded in a crystalline BPO 4 matrix. The electrochemical responses of ATCO and Sn 0.72[BPO 4] 0.28 composite in galvanostatic mode show reversible capacities of about 450 and 530 mAh g -1, respectively, with different irreversible capacities (60% and 29%). Analysis of these composite materials by 119Sn Mössbauer spectroscopy in transmission (TMS) and emission (CEMS) modes confirms that ATCO is an amorphous Sn II composite oxide and shows that in the case of Sn 0.72[BPO 4] 0.28, the surface of the tin clusters is mainly formed by Sn II in an amorphous interface whereas the bulk of the clusters is mainly formed by Sn 0. The determination of the recoilless free fractions f (Lamb-Mössbauer factors) leads to the effective fraction of both Sn 0 and Sn II species in such composites. The influence of chemical composition and especially of the surface-to-bulk tin species ratio on the electrochemical behaviour has been analysed for several Sn x[BPO 4] 1-x composite materials (0.17BPO 4] 0.28 as active material exhibits interesting electrochemical performances (reversible capacity of 500 mAh g -1 at C/5 rate).

  3. Reuse of hazardous calcium fluoride sludge from the integrated circuit industry.

    Science.gov (United States)

    Zhu, Ping; Cao, Zhenbang; Ye, YiLi; Qian, Guangren; Lu, Bo; Zhou, Ming; Zhou, Jin

    2013-11-01

    The Chinese integrated circuit industry has been transformed from a small state-owned sector into a global competitor, but chip manufacturing produces large amounts of calcium fluoride sludges (CFS). In China, landfill is a current option for treating CFS. In order to solve the problem of unavailable landfill sites and prevent fluorine from dissolved CFS polluting water sources, CFS was tested as a component for a ceramic product made with sodium borate, sodium phosphate and waste alumina using a low-temperature sintering technology, and the effects of various factors on characteristics of the ceramic were investigated to optimize the process. The best sintering temperature was controlled at 700°C, and the optimal raw material ratio of the ceramic was 11% sodium borate, 54% sodium phosphate, 30% CFS and 5% waste alumina. The CFS ceramic was characterized by a morphological structure and X-ray diffraction. The results indicated that CFS was transformed into Na2Ca(PO4)F as an inert and a main crystalline phase in the ceramic, which was enclosed by the borophosphate glass. Toxicity characteristic leaching procedure, corrosion resistance and compressive strength tests verified CFS ceramic as a qualified construction ceramic material, and the fluorine from CFS was solidified in the inert crystalline phase, which would not be released to cause secondary pollution. This novel technology not only avoids the CFS hydrolyzing reaction forming harmful hydrofluoric acid gas at 800°C and above, but also produces high-performance ceramics as a construction material, in accordance with the concept of sustainable development. PMID:24025370

  4. Silver diaquacobalt(II catena-borodiphosphate(V hydrate, (Ag0.79Co0.11Co(H2O2[BP2O8]·0.67H2O

    Directory of Open Access Journals (Sweden)

    Hafid Zouihri

    2012-01-01

    Full Text Available The structure of the title compound, (Ag0.79Co0.11Co(H2O2[BP2O8]·0.67H2O is isotypic to that of its recently published counterparts AgMg(H2O2[BP2O8]·H2O and (Ag0.57Ni0.22Ni(H2O2[BP2O8]·0.67H2O. It consists of infinite borophosphate helical ribbons [BP2O8]3−, built up from alternate BO4 and PO4 tetrahedra arranged around the 65 screw axes. The vertex-sharing BO4 and PO4 tetrahedra form a spiral ribbon of four-membred rings in which BO4 and PO4 groups alternate. The ribbons are connected through slightly distorted CoO4(H2O2 octahedra whose four O atoms belong to the phosphate groups. The resulting three-dimensional framework is characterized by hexagonal channels running along [001] in which the remaining water molecules are located. The main difference between the Mg-containing and the title structure lies in the filling ratio of Wyckoff positions 6a and 6b in the tunnels. The refinement of the occupancy rate of the site 6a shows that it is occupied by water at 67%, while the refinement of that of the site 6b shows that this site is partially occupied by 78.4% Ag and 10.8% Co, for a total of 82.2%. The structure is stabilized by O—H...O hydrogen bonds between water molecules and O atoms that are part of the helices.

  5. Silver(I diaquanickel(II catena-borodiphosphate(V hydrate, (Ag0.57Ni0.22Ni(H2O2[BP2O8]·0.67H2O

    Directory of Open Access Journals (Sweden)

    Hafid Zouihri

    2011-08-01

    Full Text Available The structure framework of the title compound, (Ag0.57Ni0.22Ni(H2O2[BP2O8]·0.67H2O, is the same as that of its recently published counterpart AgMg(H2O2[BP2O8]·H2O. In the title structure, the Ag, Ni, B and one O atom are located on special positions (sites symmetry 2. The structure consists of infinite borophosphate helical [BP2O8]3− ribbons, built up from alternate BO4 and PO4 tetrahedra arranged around the 65 screw axes. The vertex-sharing BO4 and PO4 tetrahedra form a spiral ribbon of four-membered rings in which BO4 and PO4 groups alternate. The ribbons are connected through slightly distorted NiO4(H2O2 octahedra, four O atoms of which belong to the phosphate groups. The resulting three-dimensional framework is characterized by hexagonal channels running along [001]. However, the main difference between the structures of these two compounds lies in the filling ratio of Wyckoff positions 6a and 6b in the tunnels. Indeed, in this work, the refinement of the occupancy rate of sites 6a and 6b shows that the first is occupied by water at 67% and the second is partially occupied by 56.6% of Ag and 21.6% of Ni. In the AgMg(H2O2[BP2O8]·H2O structure, these two sites are completely occupied by H2O and Ag+, respectively. The title structure is stabilized by O—H...O hydrogen bonds between water molecules and O atoms that are part of the helices.

  6. Reuse of hazardous calcium fluoride sludge from the integrated circuit industry.

    Science.gov (United States)

    Zhu, Ping; Cao, Zhenbang; Ye, YiLi; Qian, Guangren; Lu, Bo; Zhou, Ming; Zhou, Jin

    2013-11-01

    The Chinese integrated circuit industry has been transformed from a small state-owned sector into a global competitor, but chip manufacturing produces large amounts of calcium fluoride sludges (CFS). In China, landfill is a current option for treating CFS. In order to solve the problem of unavailable landfill sites and prevent fluorine from dissolved CFS polluting water sources, CFS was tested as a component for a ceramic product made with sodium borate, sodium phosphate and waste alumina using a low-temperature sintering technology, and the effects of various factors on characteristics of the ceramic were investigated to optimize the process. The best sintering temperature was controlled at 700°C, and the optimal raw material ratio of the ceramic was 11% sodium borate, 54% sodium phosphate, 30% CFS and 5% waste alumina. The CFS ceramic was characterized by a morphological structure and X-ray diffraction. The results indicated that CFS was transformed into Na2Ca(PO4)F as an inert and a main crystalline phase in the ceramic, which was enclosed by the borophosphate glass. Toxicity characteristic leaching procedure, corrosion resistance and compressive strength tests verified CFS ceramic as a qualified construction ceramic material, and the fluorine from CFS was solidified in the inert crystalline phase, which would not be released to cause secondary pollution. This novel technology not only avoids the CFS hydrolyzing reaction forming harmful hydrofluoric acid gas at 800°C and above, but also produces high-performance ceramics as a construction material, in accordance with the concept of sustainable development.

  7. Fixation of Simulated Highly Radioactive Wastes in Glassy Solids

    International Nuclear Information System (INIS)

    Current laboratory development work at ORNL aims at incorporating high-activity-level wastes in high-density insoluble glasses, containing all radioactive constituents in the solid. Experiments with simulated TBP-25 (aluminium, HNOs), Purex and Darex (stainless steel, HNOs) wastes have indicated the technical feasibility of such a process. Dense, microcrystalline solids may be as acceptable as true glasses; their greater thermal conductivity compensates somewhat for the increase in surface area over that of true glasses. Phosphate and borophosphate glasses were prepared from all three types of waste in thelaboratory.Caesium volatility was limited to the — 0.1% due to physical entrainment, and ruthenium volatility was lowered to -0.5% by addition of phosphite or hypophosphite. Other additives included PbO, Ca(OH)2, NaOH, and MgO. Bulk densities varied from 2.36 to 2.90 g/cm3 for TBP-25 and from 2.63 to 2.80 g/cm3 for Purex waste. Corresponding volume reductions from the concentrated waste solutions were 7.2 -9.3 and 5.7 - 8.3; initial softening points varied from 875 to 100°C and from 830 to 975°C respectively. Darex tests are still preliminary. Semi-continuous operation on a semi-engineering scale produced a true glass from TBP-25 waste and a microcrystalline solid from Purex. The thermal conductivity of the glass varied from 1.05 BTU/hr-ft-F° at 320° F to 1.6 at 1050°F, about 10 times higher than that of the calcine without additives. Ruthenium volatility was held to <10% by phosphite addition. Stainless steel is a satisfactory material for construction of the calcination-fixation container. Essentially all the internal corrosion takes place during the relatively short (2-6 hr) period in which the last of the acid and water are expelled at the maximum temperature. Melt production increased the corrosion of 304L stainless steel from 5 to 42 mil/month for a 24-hr evaporation-fixation cycle on TBP-25 waste and from 8 to 140 mil/ month on Purex waste. Operation