Effect of hypophosphite on electrodeposition of graphite@copper powders

The effect of sodium hypophosphite (NaH₂PO₂) on the electrodeposition of copper coated graphite powders (graphite@Cu) was investigated in this paper. The cathodic polarization curves were determined by potentiodynamic scanning method in the electrolyte containing various concentrations of NaH₂PO₂. Hypophosphite could reduce the overpotential of copper deposited on the graphite particles surface and accelerate electroless copper nuclei generated by the reduction reaction. The applied potential promoted the formation of copper nuclei on the surface of graphite powders. Uniform graphite@Cu powders were fabricated by optimizing the NaH₂PO₂ concentration in the range of 10–15 g dm⁻³. The residue of NaH₂PO₂ could be depleted to less than 0.25 g dm⁻³ by decomposition on the anode and chemical reduction in the bath during electrodeposition. The effect of hypophosphite on the electrodeposition of graphite@Cu is also discussed.     

Multilayer design of hybrid phosphor film for application in LEDs

Crosslinked polydimethylsiloxane (PDMS) composite coatings containing luminescent micrometer-sized yellow Y₃Al₅O₁₂:Ce³⁺ (YAG:Ce³⁺) particles were prepared by spraying for potential applications in solid-state lighting. Blue light was down converted by phosphor particles to produce white light, yet poor color properties of YAG:Ce³⁺ stemmed from a deficiency of red. When nitride-based red phosphor was simply blended into the system, the electrostatic interaction of negatively charged YAG:Ce³⁺ and positively charged red phosphor particles caused remarkable clustering and heterogeneity in particle dispersion. Consequently, the light is dominantly blue and shifted to cold white. In other case, phosphor particles were sprayed onto the diffused polycarbonate substrate in stacked layers. Coatings with >80% inorganic content by mass with a thickness of 60 μm were subjected to thermal crosslinking, which the presence of the phosphor particles obstructed, presumably due to the hindrance of large phosphor particles in the diffusion of PDMS precursors. The coating of YAG:Ce³⁺ first followed by red phosphor in stacked layers produced better light output and color properties than the coating obtained by spraying the mixture at once. Monte Carlo simulation validated the hypothesis.     

Effect of boron waste and boric acid addition on the production of low energy belite cement

The effect of boron oxide addition on the production of low energy belite cements has been investigated. Three types of clinkers were prepared with 1.5 wt.% (BC_BA1.5) boric acid, and 1.0 wt.% (BC_BW1) and 6.5 wt.% (BC_BW6.5) boron waste addition. The design of the raw mixtures was based on modified Bogue equations. According to the free lime content and the evolution of the microstructure of the clinkers, firing was performed at 1330 °C, 1350 °C and 1310 °C for BC_BA1.5, BC_BW1 and BC_BW6.5, respectively. Boron addition favored the reduction of the clinkering temperature as well as the stabilization of upper belite polymorphs. According to the present results, late compressive strength development of belite cements depends mainly on the crystal type rather than on the content of belite in the clinker. The results indicate that controlled quantities of boron oxide can be beneficial in the production of belite cement.     

Effects of microstructural heterogeneity on very high cycle fatigue properties of 7050-T7451 aluminum alloy friction stir butt welds

In this study, the very high cycle fatigue (VHCF) properties of 7050-T7451 aluminum alloy and its friction stir welding (FSW) butt welds have been investigated. The results show that the failure of FSW joints still occurs at 7.0 × 10⁸ cycles. The fatigue properties of the FSW joints are superior to those of the base material, especially in the super long life regime. Most fatigue cracks initiate at the thermo-mechanically affected zone and heat affected zone on the advancing side of the FSW joints, and the susceptibility of these zones to fatigue is attributed to the metallurgical heterogeneity.     

Sr3Bi(PO4)3:Eu2+, Mn2+: Single-phase and color-tunable phosphors for white-light LEDs

Sr₃Bi(PO₄)₃:Eu²⁺, Sr₃Bi(PO₄)₃:Mn²⁺, and Sr₃Bi(PO₄)₃:Eu²⁺, Mn²⁺ phosphors were synthesized by solid state reaction. The structure and luminescent characteristics were investigated by X-ray powder diffraction and fluorescent spectrophotometer. All samples have the structural type of eulytine. The excitation and emission spectra of Sr₃Bi(PO₄)₃:0.01Eu²⁺ sample show characteristic bands of Eu²⁺ ions. Also, the excitation and emission spectra of Sr₃Bi(PO₄)₃:0.06Mn²⁺ sample show characteristic bands of Mn²⁺ ions. The emission color of Sr₃Bi(PO₄)₃:Eu²⁺, Mn²⁺ sample could be tuned through tuning the co-dopant concentration of Mn²⁺ ions. The decay times for the Eu²⁺ ions decrease with the increase of Mn²⁺ dopant concentration, but the energy transfer efficiency increases with the increase of Mn²⁺ dopant concentration. On the basis of the luminescent spectra and fluorescence decay curves, we confirm that the energy transfer process from the Eu²⁺ to Mn²⁺ ions takes place in the co-doped Sr₃Bi(PO₄)₃ phosphor. Sr₃Bi(PO₄)₃:Eu²⁺, Mn²⁺ sample shows the good thermostability. The emission intensity of the sample at 400 K is about 60% of the value at 300 K. These results show Sr₃Bi(PO₄)₃:Eu²⁺, Mn²⁺ phosphors could be anticipated for UV-pumped white-light-emitting diodes.     

Photoluminescence properties of Sr3(PO4)2: Eu2+, Dy3+ double-emitting blue phosphor for white LEDs

Double-emitting blue phosphor Sr₃(PO₄)₂: Eu²⁺, Dy³⁺ was synthesized by solid state reaction under H₂ atmosphere. XRD exhibited the pure hexagonal phase of the prepared phosphor. The photoluminescence results showed that all samples had intense broad absorption band between 250 and 450 nm, which matched well with the near-UV (350–420 nm) emission band of InGaN-based chips. The emission spectrum of Sr₃(PO₄)₂: Eu²⁺, Dy³⁺ consisted of two broad bands, peaked at 485 nm and 410 nm, which originated from two luminescent centers, related to 4f⁶5d¹ → 4f⁷ transition of Eu²⁺ in six-coordinated Sr(I) and ten-coordinated Sr(II) sites respectively. The intensity ratio of two emission bands could be easily tuned by adjusting Dy³⁺ co-doping content, which resulted in color-tunable luminescence in bluish green region to purplish blue region.     

Tunable luminescence properties and energy transfer of single-phase Ca<Subscript>4</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>O: Dy<Superscript>3+</Superscript>, Eu<Superscript>2+</Superscript> multi-color phosphors for warm white light

The novel Ca_4?x(PO₄)₂O: xDy³⁺ and Ca_4?x?y(PO₄)₂O: xDy³⁺, yEu²⁺ multi-color phosphors were synthesized by traditional solid-state reaction. The crystal structure, particle morphology, photoluminescence properties and energy transfer process were investigated in detail. The X-ray diffraction (XRD) results demonstrate that the products showed pure monoclinic phase of Ca₄(PO₄)₂O when x < 0.1. The scanning electron microscopy (SEM) indicated that the phosphors were grain-like morphologies with diameters of ~ 3.7–7.0 μm. Under excitation of 345 nm, Dy³⁺-doped Ca₄(PO₄)₂O phosphors showed multi-color emission bands at 410, 481 and 580 nm originated from oxygen vacancies and Dy³⁺. Interestingly, Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors exhibited blue emission band at 481 nm and broad emission band from 530 to 670 nm covering green to red regions. The energy transfer process from Dy³⁺ to Eu²⁺ was observed for the co-doped samples, and the energy transfer efficiency reached to 60% when Eu²⁺ molar concentration was 8%. In particular, warm/cool/day white light with adjustable CCT (2800–6700 K) and high CRI (R_a > 85) can be obtained by changing the Eu²⁺ co-doping contents in Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors. The optimized Ca_3.952(PO₄)₂O: 0.04Dy³⁺, 0.008Eu²⁺ phosphor can achieve the typical white light with CCT of 4735 K and CRI of 87.     

Effects of surface washing on the mitigation of concrete corrosion under sewer conditions

This study systematically investigated the potential of mitigating sulfide induced sewer concrete corrosion by surface washing. Washing interrupted the corrosion activity of concrete coupons by increasing the surface pH and decreasing the H₂S uptake rates (SUR). The SUR recovered to the level prior to washing within 60–140 days. The slowest recovery rate was from the most severely corroded coupon. However, no significant difference was observed for concrete mass loss of the washed and unwashed coupons after 54 months. The results suggest that frequent washing at short intervals of a few months might be needed to control corrosion over a long term.     

Synthesis and luminescence properties of Ca8NaGd(PO4)6F2: Eu2+, Mn2+ for white LEDs

A series of luminescent emission-tunable phosphors Ca₈NaGd(PO₄)₆F₂: Eu²⁺, Mn²⁺ have been prepared by a combustion-assisted synthesis method. The X-ray diffraction measurement results indicate that the crystal structure of the phosphor is a single phase of Ca₈NaGd(PO₄)₆F₂. The photoluminescence (PL) properties of Eu²⁺ and Mn²⁺-codoped Ca₈NaGd(PO₄)₆F₂ phosphors were also investigated. The phosphors can be efficiently excited by ultraviolet (UV) light and show a blue emission band at about 450 nm and a yellow emission band at about 574 nm, which originated from the Eu²⁺ ions and the Mn²⁺ ions, respectively. The efficient energy transfer from the Eu²⁺ ions to the Mn²⁺ ions was observed and its mechanism should be a resonant type via a nonradiative dipole–quadrupole interaction. A color-tunable emission in Ca₈NaGd(PO₄)₆F₂ phosphors can be realized by Eu²⁺ → Mn²⁺ energy transfer. Our results indicate that the developed phosphor may be used as a potential white emitting phosphor for UV based white LEDs.     

Abnormal blue-shift of Eu2+-activated calcium zirconium phosphates CaZr4(PO4)6

The electronic structure of CaZr₄(PO₄)₆ was calculated using the CASTEP code and the band gap for CaZr₄(PO₄)₆ can reach up to 4.30 eV. Ca_1−xEu_xZr₄(PO₄)₆ (0.01 ⩽ x ⩽ 1) samples were prepared by a high temperature solid-state reaction method. XRD analysis shows that Eu²⁺ ion can be totally incorporated into CaZr₄(PO₄)₆ forming complete solid solutions with trigonal lattice. Ca_1−xEu_xZr₄(PO₄)₆ (0.01 ⩽ x ⩽ 1) shows typical broad band emission in wavelength range from 400 to 650 nm for both under ultraviolet (UV) light and X-ray excitation, originating from the 4f⁶5d¹ → 4f⁷5d⁰ transition of Eu²⁺ ions. With increasing Eu²⁺ concentration, there is abnormal blue-shift of the emission peaks for Ca_1−xEu_xZr₄(PO₄)₆ due to the decreasing crystal field strength and Stokes shift. With increasing temperature in CaZr₄(PO₄)₆: Eu²⁺, its emission bands show the anomalous blue-shift with decreasing intensity. The overall scintillation efficiency of Ca_0.9Eu_0.1Zr₄(PO₄)₆ is 1.7 times of that of Bi₄Ge₃O₁₂ (BGO) powder under the same conditions. In addition, its predominant decay time is about 50 ns at room temperature. The potential application of Eu²⁺-doped CaZr₄(PO₄)₆ has been pointed out.     

Phosphors based on NaZr2(PO4)3-type calcium and strontium phosphates activated with Eu2+ and Sm3+

Ca_0.5Zr₂(PO₄)₃:Eu²⁺, Sr_0.5Zr₂(PO₄)₃:Eu²⁺, and Ca_0.5Zr₂(PO₄)₃:Eu²⁺, Sm³⁺ orthophosphates prepared through precipitation using sol-gel processes are analogs of NaZr₂(PO₄)₃ (NZP) and crystallize in space group R $\bar 3$ . Their crystallographic parameters determined by X-ray diffraction are consistent with the interatomic distances extracted from EXAFS data. Their luminescence spectra obtained under excitation in the range 300?C400 nm contain emission bands between 425 and 525 nm. Substitution of the larger sized cations Eu²⁺ and Sm³⁺ for Ca²⁺ shifts the emission bands to shorter wavelengths and reduces their width because of the decrease in the effect of the crystal field. Analysis of the spectra indicates that Eu²⁺ occupies two types of crystallographic sites (independent interstitial sites of different sizes and shapes in the NZP framework structure). Codoping with Eu and Sm has ensured luminescence with chromaticity coordinates approaching those of white light: (x = 0.27, y = 0.34).     

Novel blue-emitting phosphor NaMg4(PO4)3:Eu, Ce with energy transfer

A blue-emitting phosphor of NaMg₄(PO₄)₃:Eu²⁺, Ce³⁺ was prepared by a combustion-assisted synthesis method. The phase formation was confirmed by X-ray powder diffraction measurement. Photoluminescence excitation spectrum measurements show that the phosphor can be excited by near UV light from 230 to 400 nm and presents a dominant luminescence band centered at 424 nm due to the 4f⁶5d¹ → 4f⁷ transition of Eu²⁺ ions at room temperature. Effective energy transfer occurs in Ce³⁺/Eu²⁺ co-doped NaMg₄(PO₄)₃ due to large spectral overlap between the emission of Ce³⁺ and excitation of Eu²⁺. Co-doping of Ce³⁺ enhances the emission intensity of Eu²⁺ greatly by transferring its excitation energy to Eu²⁺, and Ce³⁺ plays a role as a sensitizer. Ce³⁺-Eu²⁺ co-doped NaMg₄(PO₄)₃ powders can possibly be applied as blue phosphors in the fields of lighting and display.     

Corrosion resistance of strain-hardening steel-fiber-reinforced cementitious composites

This study investigated the corrosion resistance of strain-hardening steel-fiber-reinforced cementitious composites (SH-SFRCs) in a chloride environment. Two types of steel fibers, hooked and twisted, were added (2% by volume) to a high-strength mortar matrix (90 MPa). All the specimens were exposed to cyclic wetting in a 3.5% chloride solution followed by drying. The corrosion resistance of SH-SFRCs was then evaluated by measuring the direct tensile resistance after the chloride cycles. The strain capacity and toughness of all the SH-SFRCs decreased significantly after 105 chloride cycles, whereas a slight reduction was observed in their post-cracking strength. The corrosion resistance of SH-SFRCs after the chloride cycles was strongly dependent on the width of multiple microcracks when the SH-SFRCs were pre-cracked by tensioning until 0.1% tensile strain. The addition of calcium nitrite (CNI) was successful in improving the corrosion resistance of the pre-cracked SH-SFRCs in the chloride environment.     

One-way Fluid Structure Interaction modelling methodology for boiler tube fatigue failure

A modelling methodology developed for dealing with fatigue failures on large boiler tube assemblies, as used by power generation industries, is described. Boiler tube fatigue failures are resultant to a coupled combination of fluid flow and heat transfer mechanisms, inducing thermal expansion leading to fatigue failure. A combination of modelling tools is effectively combined for one-way Fluid Structure Interaction, solving for and extracting stress results efficiently. A one dimensional fluid solver is used to approximate and model the thermal flow components. The study case considered implemented the developed methodology on a quarter boiler hopper section made up of 3022 tube and membrane structure with a collective length of 4787 m. Operating conditions are iteratively adjusted in the one dimensional pipe flow model until a correlation is formed with instrumented data. This validated model enables further use for various postulated plant conditions and operational sequences through transient start-up conditions. The boiler tube temperatures obtained from the one dimensional model are transferred and used as boundary conditions in a full three dimensional finite element analysis where deformations are solved for and stress results obtained due to thermal expansion within the boiler tube walls and the adjacent support structure. The model is used for redesign of sections of the boiler to reduce stress in those areas and subsequently reduce fatigue failures.     

The use of mindmapping software for patent search and management

Modern information technologies and in particular the internet have revolutionized the patent information professionals' work in terms of speed of access and information comprehensiveness from both company internal and external digital sources. Here, I describe how the digital mindmapping technique can be used to complement existing intellectual property management software solutions to meet the challenge of optimizing and managing patent search workflows as well as to rapidly organise and access highly dynamic, heterogeneous and scattered patent information sources. Both eye catching and highly memorable and at the same time self-explanatory mindmapping examples are presented. These were designed to include basic and advanced level digital mindmapping features tailored to significantly speed up and maintain a high work quality level of patent search professionals. A special emphasis is put on the great benefit of organising and accessing the plethora of internet-based worldwide online patent registers through mindmapping, both in terms of managing the constantly changing deep links to the actual search options for e.g., legal status information, and keeping track of the offered level of content.     

The optical spectroscopic properties of rare earth-activated barium orthophosphate in VUV-Vis range

The optical properties of rare earth ions-activated barium orthophosphate phosphors, Ba₃(PO₄)₂:RE (RE=Ce³⁺, Sm³⁺, Eu³⁺, Eu²⁺, and Tb³⁺), were investigated in vacuum ultraviolet (VUV)-Vis range. A band-band transition of PO₄³⁻ in Ba₃(PO₄)₂ is observed in the region of 150-170 nm. The partial reduction of Eu³⁺ to Eu²⁺ was observed and confirmed by luminescent spectra under the VUV-UV excitation. It is proposed that the electronegative defects that formed by aliovalent substitution of Eu³⁺ on the Ba²⁺ site in the host are responsible for the reduction process.     

A potential Eu-activated Ca10K(PO4)7 red phosphor for white light-emitting diodes

New red Ca₁₀K(PO₄)₇:Eu³⁺, K⁺ phosphors were synthesized by solid state reaction and their photoluminescence properties as well as those by co-doping Mo⁶⁺ under near ultraviolet excitation were investigated. From the excitation spectra monitored at 611 nm, it can be seen that the strongest excitation peak is situated at 393 nm, well matching with the emission wavelength of near-ultraviolet chips for white LEDs. Upon 393 nm excitation, the brightness of Ca₉K(PO₄)₇:0.5Eu³⁺, 0.5 K⁺ with the optimal Eu³⁺-doping concentration is about 2.3 times stronger than that of the commercial red Y₂O₃:Eu³⁺ phosphor. The introducing of Mo⁶⁺, which results in a possible variety for the excited energy level of the host, can enhance the brightness of Eu³⁺ to be maximized by about 15%. The CIE chromaticity coordinates of Ca₉K(PO₄)₇:0.5Eu³⁺, 0.5 K⁺ are calculated to (0.654, 0.345), which are close to the (0.67, 0.33) standard of the National Television System Committee. All the above results indicate Eu³⁺-activated Ca₁₀K(PO₄)₇ is a potential candidate for white LEDs.     

Luminescence properties and energy transfer of Ba2Mg(PO4)2:Eu2+, Mn2+ phosphor synthesized by co-precipitation method

The Ba₂Mg(PO₄)₂:Eu²⁺, Mn²⁺ phosphor is synthesized by a co-precipitation method. Crystal phase, morphology, excitation and emission spectra of sample phosphors are analyzed by XRD, SEM and FL, respectively. The results indicate particles synthesized by a co-precipitation method have a smaller size in diameter than that synthesized by conventional solid-state reaction method. Emission spectra of BMP:Eu²⁺, Mn²⁺ phosphor show a broad blue and a broad yellow emission bands with two peaks at about 456 nm and 575 nm under 380 nm excitation. An overlap between Eu²⁺ emission band and Mn²⁺ excitation band proves the existence of energy transfer from Eu²⁺ to Mn²⁺. Emitting color of the BMP:Eu²⁺, Mn²⁺ phosphor could be tuned by adjusting relative contents of Eu²⁺ and Mn²⁺ owing to energy transfer formula. Therefore, BMP:Eu²⁺, Mn²⁺ may be considered as a potential candidate for phosphor for near-UV white LED.     

Thermal conductivity of silver loaded conductive epoxy from cryogenic to ambient temperature and its application for precision cryogenic noise measurements

The pressure to increase the sensitivity of instrumentation has pushed the use of cryogenic Low Noise Amplifier (LNA) technology into a growing number of fields. These areas range from radio astronomy and deep space communications to fundamental physics. In this context manufacturing for cryogenic environments requires a proper thermal knowledge of the materials to be able to achieve adequate design behavior. In this work, we present experimental measurements of the thermal conductivity of a silver filled conductive epoxy (EPO-TEK H20E) which is widely used in cryogenic electronics applications. The characterization has been made using a sample preparation which mimics the practical use of this adhesive in the fabrication of cryogenic devices. We apply the data obtained to a detailed analysis of the effects of the conductive epoxy in a monolithic thermal noise source used for high accuracy cryogenic microwave noise measurements. In this application the epoxy plays a fundamental role since its limited thermal conductivity allows heating the chip with relatively low power. To our knowledge, the cryogenic thermal conductivity data of this epoxy has not been reported before in the literature in the 4–300 K temperature range. A second non-conductive epoxy (Gray Scotch-Weld 2216 B/A), also widely used in cryogenic applications, has been measured in order to validate the method by comparing with previous published data.     

Synthesis and luminescence properties of Eu2+- and Mn2+-activated Mg21Ca4Na4(PO4)18 phosphors

Rare earth-doped phosphates have attracted much attention in recent years because of their interesting optical applications. However, few studies have reported on optical properties of fillowite-like compounds. Eu²⁺ and Mn²⁺ singly doped and Eu²⁺/Mn²⁺-codoped Mg₂₁Ca₄Na₄(PO₄)₁₈ phosphors were synthesized for the first time via combustion-assisted synthesis technique. The Eu²⁺-activated sample emits an intense blue light under 360 nm excitation, while the Eu²⁺/Mn² + -codoped Mg₂₁Ca₄Na₄(PO₄)₁₈ sample exhibits a broad blue emission band and a red emission band, resulting from Eu²⁺ and Mn²⁺, respectively. Energy transfer between Eu²⁺ and Mn²⁺ was discovered and the transfer efficiency was also estimated based on relative intensities of Eu²⁺ and Mn²⁺ emission. Thus, the relative strength of blue and red emission intensities could be tuned by varying the relative concentration of Eu²⁺ and Mn²⁺. Since the photoluminescence excitation spectra of the newly developed Mg₂₁Ca₄Na₄(PO₄)₁₈:Eu²⁺, Mn²⁺ phosphors exhibit a strong absorption in the range of 250–400 nm, they are promising for producing UV-LED-based white LEDs.