离子交换水软化技术研究与应用进展

离子交换法是目前最常见的水软化技术之一，其基于可逆的离子交换反应将溶液中的硬度离子选择性去除，属于典型的特种分离过程。本文介绍并总结了离子交换水软化的基本原理、水软化用离子交换树脂的结构和分类、离子交换水软化技术研究和应用，并针对离子交换水软化存在的问题提出了相应的解决思路。     

Structural studies on Ca3Al4MgO10 (C3A2M)—A ternary phase in the system CaO–Al2O3–MgO

In a sequence of temperature-dependent solid-state reactions in the system CaO–Al₂O₃–MgO the formation of the ternary phase Ca₃Al₄MgO₁₀ or C₃A₂M has been studied. Whereas the compound could not be prepared at 1200°C, a yield of 85 wt.-% of Ca₃Al₄MgO₁₀ was obtained at 1320°C (incongruent melting point: 1330°C). Powder diffraction data compare well with results of previous investigations from the 1960s. Single crystals of Ca₃Al₄MgO₁₀ could be retrieved from the sinter-pellets. Basic crystallographic data are as follows: orthorhombic symmetry, space group Pbcm, a = 5.14073(8), b = 16.7576(2), c = 10.70977(16) Å, V = 922.61(2) ų, Z = 4. Using synchrotron diffraction data it was possible to solve the crystal structure. Least-squares refinements resulted in a residual of R(|F|) = 0.021 for 1000 independent observed reflections with I > 2σ(I) and 97 parameters. The structure contains [TO₄]-tetrahedra (T=Al,Mg) forming a three-dimensional (3-D) framework whose topological characteristics have been determined. Al-Mg distributions on the different T-sites have been studied. The calcium cations are located in voids of the network. More than 50 years after its first observation our investigation clarifies the crystal structure of a compound belonging to a system that is of relevance for several fields of materials science.     

Modified embedded-atom method interatomic potential for the Mg–Zn–Ca ternary system

Mg–Zn–Ca alloys are representative Mg alloys with high formability at room temperature. Their high formability is thought to be related to slip, twinning, and recrystallization of the alloys, but the detailed mechanisms have not yet been clarified. To enable atomistic simulations for investigating those behaviors, an interatomic potential for the Mg–Zn–Ca ternary system was developed. The development was based on the second nearest-neighbor modified embedded-atom method formalism, combining previously developed Mg–Zn and Mg–Ca potentials with the newly developed Zn–Ca binary potential. The Zn–Ca and Mg–Zn–Ca potentials reproduce structural, elastic, and thermodynamic properties of compounds and solution phases of relevant alloy systems in reasonable agreement with experimental data, first-principles and CALPHAD calculations. The applicability of the developed potentials is demonstrated through calculations of the effects of Zn and Ca solutes on the generalized stacking fault energy for various slip systems, segregation energy on twin boundaries, and volumetric misfit strain.     

Dielectric,ferroelectric, and piezoelectric properties of lead-free Ba0.95Ca0.05Ti1-xZrxO3 ceramics

Abstract

Ba_0.95Ca_0.05Ti_1-xZr_xO₃ (BCTZO) ceramics were prepared by a solid state reaction method. The samples were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM) and X-ray absorption near edge structure (XANES). The ceramics exhibit a pure perovskite structure. The average grain size gradually decreases with increasing Zr concentration. XANES results indicate that the intensities of pre-edge peaks dropped with increasing Zr concentration. The BCTZO ceramic of x?=?0.05 has the optimum electrical properties with the maximum dielectric constant (ε'_m), remanent polarization (2P_r), coercive electric field (2E_c) and piezoelectric charge constant (d₃₃) of 7,244, 12.54 (μC/cm²), 5.29 (kV/cm) and 288 (pC/N), respectively.     

Improvement in hydration resistance of CaO granules by addition of Zr(OH)4 and Al(OH)3

Improving the hydration resistance of CaO aggregates is the key to successful application of lime-based refractories in metallurgical industry. Additive Zr(OH)₄ and Al(OH)₃ were introduced in the preparation of CaO granules using granulation equipment and calcination method in this study. The results showed that the hydration resistance of CaO granules was improved significantly, especially for granules with 0.6 wt.% Zr(OH)₄ and 0.9 wt.% Al(OH)₃, respectively. The shell of CaO granules was relatively dense after calcination and the volume of open pores of CaO granules decreased from 3.56 × 10⁻² to 1.80 × 10⁻² cm³/g when additive was introduced. Zr(OH)₄ and Al(OH)₃ have the opposite effect on the closed porosity of CaO granules, the closed porosity of CaO granules was decreased with Zr(OH)₄ addition, but increased with Al(OH)₃ addition.     

Significantly enhanced breakdown field in Ca1-xSrxCu3Ti4O12 ceramics by tailoring donor densities

Significantly enhanced breakdown field of 24.52 kV cm^?1 as well as noteworthy nonlinear coefficient of 8.11 and low dielectric loss of 0.077 were obtained in Ca_0.6Sr_0.4Cu₃Ti₄O₁₂ ceramic. It was proved from impedance spectra that improved breakdown field was attributed to enhanced grain boundary resistance and elevated Schottky barrier height, which was further found resulting from reduced donor densities in C-V measurements. In addition, it was found that the activation energy originated from oxygen vacancies was increased, indicating the generation of oxygen vacancies was suppressed. Since oxygen vacancies acted as donors in depletion layers, it is reasonable to deduce that the reduced donor density was mainly ascribed to the decreased oxygen vacancies. In conclusion, maximum integrated action of strong solid solution effect and weak Sr-stretching effect was achieved when Sr/Ca ratio is 40/60, leading to greatly elevated potential barrier height and enhanced breakdown field consequently.     

Influence of trace Ca addition on texture and stretch formability of AM50 magnesium alloy sheet

The AM50, AM50–0.1Ca, AM50–0.3Ca and AM50–0.5Ca (wt.%) alloys were hot-rolled and their mechanical properties were determined for the purpose of investigating the effect of trace Ca addition on the texture and stretch formability of AM50 alloy. The results show that the addition of trace Ca can effectively modify the basal texture, which is characterized by the split of basal poles deviated from the normal direction (ND) after the hot rolling, while a broad spread of the basal planes toward the transverse direction (TD) after the annealing. Such change of the basal texture is related to the prior formation of massive compression twins and the decrease of the c/a ratio. Erichsen value increases from 2.25 to 4.21 mm with the increase of Ca content. The enhancement of stretch formability is ascribed to the weakened basal texture, which results in the increase of n-value and the decrease of r-value.     

Ca对Mg-Gd-Y-Zn-Zr合金热变形行为及热加工性能的影响

利用Gleeble3500热模拟试验机研究了Ca对Mg-Gd-Y-Zn-Zr合金在变形温度573～723 K,应变速率0.001～1 s-1的热变形行为及热加工性能的影响。结果表明:Ca增大了合金的流变应力及变形激活能,扩宽了加工安全区及最佳加工区范围,但降低了最大功率耗散因子及动态再结晶程度。结合激光共聚焦显微镜分析了合金热压缩后组织,验证了热加工图的准确性,并制定了合理的热加工工艺,Mg-Gd-Y-Zn-Zr合金的最佳加工区域为:应变速率0.001～0.01 s~(-1),温度623～723 K。根据最佳加工工艺参数获得了表面质量良好,无变形缺陷的等温锻造合金。     

Facile synthesis of the desired red phosphor Li2Ca2Mg2Si2N6:Eu2+ for high CRI white LEDs and plant growth LED device

The red emission with suitable peak wavelength and narrow band is acutely required for high color rendering index (CRI) white LEDs without at the cost of the luminous efficacy. Herein, the Li₂Ca₂Mg₂Si₂N₆:Eu²⁺ red phosphor was prepared with facile solid-state method using Ca₃N₂, Mg₃N₂, Si₃N₄, Li₃N, and Eu₂O₃ as the safety raw materials under atmospheric pressure for the first time, which shows red emission peaking at 638 nm with full width at half maximum (FWHM) of 62 nm under blue light irradiation and becomes the desired red phosphor to realize the balance between luminous efficacy and high CRI in white LEDs. The morphology, structure, luminescence properties, thermal quenching behavior, and chromaticity stability of the Li₂Ca₂Mg₂Si₂N₆:Eu²⁺ phosphor are investigated in detail. Concentration quenching occurs when the Eu²⁺ content exceeds 1.0 mol%, whereas high-temperature photoluminescent measurements show a 32% drop from the room-temperature efficiency at 423 K. In view of the excellent luminescence performances of Li₂Ca₂Mg₂Si₂N₆:Eu²⁺ phosphor, a white LEDs with CRI of 91 as a proof-of-concept experiment was fabricated by coating the title phosphor with Y₃Al₅O₁₂:Ce³⁺ on a blue LED chip. In addition, the potential application of the title phosphor in plant growth LED device was also demonstrated. All the results indicate that Li₂Ca₂Mg₂Si₂N₆:Eu²⁺ is a promising red-emitting phosphor for blue LED-based high CRI white LEDs and plant growth lighting sources.     

Ca-doped PrBa1-xCaxCoCuO5+δ (x = 0–0.2) as cathode materials for solid oxide fuel cells

Ca-doped perovskite oxides PrBa_1-xCa_xCoCuO_5+δ (PBCCCO, x = 0–0.2) were prepared and investigated as SOFC cathode materials. PBCCCO samples are single perovskite structure with P4/mmm space group. Pr, Cu and Co ions in PBCCCO samples exist in the form of Pr³⁺/Pr⁴⁺, Cu²⁺/Cu⁺ and Co³⁺/Co⁴⁺ multi-valence states. The average TECs of PBCCCO samples were reduced from 17.4 × 10^?6 K^?1 (x = 0) to 16.7 × 10^?6 (x = 0.1) and 16.1 × 10^?6 K^?1 (x = 0.2) whin RT-900°С. The electrical conductivity and electrochemical catalytic activity of PBCCCO perovskites was enhanced obviously by Ca doping. The ASR values decreased by 60.1% (@650 °C), 68.9% (@700 °C), 71.0% (@750 °C) and 72.8% (@800 °C) respectively when Ca doping content increased from x = 0 to 0.2. These results suggest PBCCCO sample with Ca doing content x = 0.2 can be a promising cathode for IT-SOFC.