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JOURNAL OF CHEMICAL THERMODYNAMICS · 2016 · IF 2.196

Stable (solid + liquid) phase equilibrium for the ternary system (NaCl + RbCl + H2O) at T = (288.15, 298.15 and 308.15) K

Yunxue Gao,Shuni Li,Quanguo Zhai,Yucheng Jiang,Mancheng Hu

The (solid   +   liquid) phase equilibrium of the ternary system (NaCl   +   RbCl   +   H 2 O) at T   =   (288.15, 298.15 and 308.15)   K was studied by the method of isothermal solution saturation. Moreover, the density and refractive index of the solution was also determined. The solid phase was studied by the Schreinemaker’s wet residue method and verified by X-ray diffraction. The results show that each of the phase diagrams contains one invariant point, two univariant curves, and three crystallization regions. The crystallization region of NaCl increased obviously with the temperature increasing, while the crystallization regions of RbCl and the mixed crystallization region of (NaCl   +   RbCl) decreased a little. Furthermore, there are break points at the invariant points for density and refractive index curves.

CAS / MDL: 143-66-8
研究领域: 化学 · 材料科学
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2025 · IF 2.1

Phase Equilibria and Phase Diagram of the Quaternary System (Na+, K+, Ca2+//Cl– -H2O) and Its Subsystems at 338.15 K

Ruxue Yao,Yang Ge,Jiangtao Song,Fei Yuan,Yafei Guo,Tianlong Deng

The Qaidam Basin has potassium- and calcium-rich oil field brine resources at high temperatures. Since the phase diagram is a powerful tool to guide the separation and purification of inorganic chemical engineering for the development of potassium resources in oil field brine, the quaternary oil field brine system (Na+, K+, Ca2+//Cl– -H2O) and its two subsystems ((Na+, Ca2+//Cl– -H2O) and (K+, Ca2+, //Cl– -H2O)) at 338.15 K were reported for the first time by the isothermal dissolution equilibrium method. The compositions of the equilibrium solid phases were analyzed and identified by combined chemical analyzing and X-ray diffraction. The quaternary system has four crystallized regions corresponding to NaCl, KCl, KCl·CaCl2, and CaCl2·2H2O at 338.15 K, and the incongruent double salt KCl·CaCl2 occurred at 338.15 K. The study facilitates the enrichment of thermodynamic data and exploits brine-based potassium resources.

CAS / MDL: 7647-14-5 7447-40-7
研究领域: 化学工程 · 无机化学
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Asia-Pacific Journal of Chemical Engineering · 2020 ·Vol. 16 ·期 2 ·e2595 · IF 1.06

Solid–liquid equilibria in the quaternary system LiBr−NaBr−KBr−H2O and its two ternary subsystems at 288.15 K

Xiao-Yun Qi,Chun-Xia He,Shi-Hua Sang,Jia Liu,Yun-Yun Gao

The solubilities of the LiBr−NaBr−KBr−H 2 O system and its subsystems LiBr−NaBr−H 2 O and LiBr−KBr−H 2 O were investigated at 288.15 K by the isothermal dissolution equilibrium method, and the corresponding phase diagrams were plotted, respectively. In the three systems, neither solid solution nor double salt was found. For the first subsystem LiBr−NaBr−H 2 O, there are two invariant points, three dissolution equilibrium curves, and three crystallization regions, which are LiBr·2H 2 O, NaBr·2H 2 O, and NaBr. An invariant point, two dissolution equilibrium curves, and two crystallization regions, which are LiBr·2H 2 O and KBr, constitute the stable phase diagram of the second subsystem LiBr−KBr−H 2 O. The phase diagram of the quaternary system LiBr−NaBr−KBr−H 2 O consists of two invariant points, five solubility curves, and four regions in which are LiBr·2H 2 O, NaBr, NaBr·2H 2 O, and KBr.

CAS / MDL: 7550-35-8
研究领域: 化学 · 物理化学
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JOURNAL OF CHEMICAL ENGINEERING OF JAPAN · 2020 ·Vol. 53 ·期 5 ·183-189 · IF 0.651

Studies of Phase Equilibria in Ternary KBr–SrBr2–H2O and NaBr–SrBr2–H2O Systems at 308 K

Chao Ye,Yun-Yun Gao,Shi-Hua Sang,Pei-Huan Jiang,Qi Ge

The phase equilibria of the KBr–SrBr2–H2O and NaBr–SrBr2–H2O ternary systems at 308 K were measured using the isothermal dissolution equilibrium method. The compositions of the liquid and solid phases were expressed as the mass fraction, and the phase diagrams constructed from the experimental data show that both ternary systems are simple co-saturated types with only one invariant point, two univariant curves, and two crystallization regions. Neither of the two ternary systems forms a double-salt or solid solution. The solid-phase crystallization regions of the KBr–SrBr2–H2O ternary system correspond to KBr and SrBr2·6H2O, and the invariant point of the NaBr–SrBr2–H2O ternary system is saturated with NaBr·2H2O and SrBr2·6H2O. From the phase diagrams, the salting-out effect of SrBr2 on KBr is clear, which indicates that the solubility of KBr is lower and it is easier to separate KBr from solution in the ternary KBr–SrBr2–H2O system at 308 K.

研究领域: 化学热力学 · 无机化学
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Journal of Materials Chemistry B · 2021 ·Vol. 10 ·期 1 ·120-130 · IF 6.331

A programmable bilayer hydrogel actuator based on the asymmetric distribution of crystalline regions

Xiaojun Li,Yue Cheng,Jianfeng Zhang,Yarui Hou,Xiaojuan Xu,Qingye Liu

A novel strategy to fabricate bilayer hydrogel actuators based on the asymmetric distribution of crystalline regions across the bilayer structures was proposed. By employing PVA polymer chains into an alkali solvent-derived chitosan hydrogel matrix, chitosan/PVA hybrid bilayer hydrogels with both excellent responsive bending and mechanical properties were obtained as pH-controlled manipulators. In the design, the chitosan/PVA hydrogels upon treatment with freeze-thawing cycles were taken as the first monolayer, where excessive crystalline regions appeared. The original chitosan/PVA hydrogel as the second monolayer was then integrated into one bilayer device through the chemical-crosslinking of epichlorohydrin at the interface. The results showed that the resultant chitosan/PVA bilayer hydrogel actuator with a weight ratio of 3 : 1 displayed better sensitivity upon exposure to stimuli. The actuation behaviors are strongly dependent on experimental parameters such as the pH, PVA content and the chemical-crosslinking density. It is proposed that the driving force originates from the asymmetric distribution of crystalline regions, thus resulting in differential swelling ratios between the monolayers. In addition, programmable 3D shape transformations were achieved by using the bilayer hydrogel with designed 2D geometric patterns, and the tailored gripper-like hydrogel actuator can successfully capture and transport the cargo. Moreover, this actuation behavior can be erased and re-written on demand under certain conditions. Taking advantage of this universal strategy, more attractive actuators derived from synthetic or natural polymers in combination with PVA are highly expected, which can be used as smart soft robots in various fields such as manipulators, grippers, and cantilever sensors.

研究领域: 材料科学 · 生物医学工程
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POLYMER · 2024 · IF 4.1

Co-vulcanization of natural rubber and Eucommia ulmoides gum for mediation of the nonlinear rheology behaviors

Zhaopeng Hu,Xin Jiang,Benteng Liu,Qiao Li,Hongda Meng,Yihu Song,Yongzhong Bao,Qiang Zheng

Co-vulcanization of natural rubber (NR) and high-moduli Eucommia ulmoides gum (EUG) is promising while the reduction in crystallinity of crosslinked EUG is adverse for developing high-performance materials. Proposed herein is a novel method to prepare high-strength and high-stretchability NR/EUG vulcanizates with rapid vulcanization of EUG into slightly crosslinked particles, followed by further vulcanization of NR to form crosslinked matrix network. Deep eutectic solvents (DESs) are employed to facilitate the vulcanization of EUG during its blending with NR. The two-step vulcanization results in vulcanizates exhibiting superior mechanical properties under shear, tensile, and compressive conditions, significantly exceeding those of vulcanizates prepared by traditional processing methods. The reinforcement mechanism is elucidated by controlling thermomechanical coupling conditions and is supported by comprehensive structural characterizations. It is suggested that the EUG crystalline regions, maintained through the special processing method, work in conjunction with the stress-induced crystallization of the matrix to enhance the vulcanizates, nearly doubling the deformation stress at 800 % strain. The crystalline regions can mediate the deformation stress during shear and compression and weaken nonlinear rheological behavior. The established structure-performance relationship is guidable for preparing high-performance NR/EUG blend vulcanizates.

CAS / MDL: 1643-19-2
研究领域: 材料科学 · 聚合物科学 · 流变学
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2024 · IF 2.2

Phase equilibria in the RbX/CsX + CuX2 + H2O (X = Cl, Br) systems at T = 298.15 K and the standard enthalpies of formation of seven double salts

Yufeng Tang,Qichao Yang,Zhanping Qiao

The phase equilibrium of ternary systems RbX/CsX + CuX 2  + H 2 O (X = Cl, Br) at T  = 298.15 K were investigated by the isothermal dissolution equilibrium method, in which the composition of equilibrium solid phases was determined by the Schreinemaker’s wet residue method. In the system RbCl + CuCl 2  + H 2 O, there were three crystallization regions corresponding to RbCl, Rb 2 CuCl 4 ·2H 2 O and CuCl 2 ·2H 2 O, respectively. Five crystallization fields corresponding to CsCl, CsCuCl 3 , Cs 3 Cu 2 Cl 7 ·2H 2 O, Cs 2 CuCl 4 and CuCl 2 ·2H 2 O were formed in the system CsCl + CuCl 2  + H 2 O. The ternary system RbBr + CuBr 2  + H 2 O had three crystalline regions corresponding to RbBr, Rb 2 CuBr 4 ·2H 2 O and CuBr 2 . In the system CsBr + CuBr 2  + H 2 O, the solid-phases of CsCuBr 3 , Cs 2 CuBr 4 , besides CsBr and CuBr 2 , were discovered. The results were compared with available literature data for cesium bromide/copper bromide salt-water system. The seven new solid phase were characterized using the X-ray diffraction method and thermogravimetric/differential analysis. The dissolution enthalpies of Rb 2 CuCl 4 ·2H 2 O, Rb 2 CuBr 4 ·2H 2 O, CsCuCl 3 , Cs 3 Cu 2 Cl 7 ·2H 2 O, Cs 2 CuCl 4 , CsCuBr 3 and Cs 2 CuBr 4 at T  = 298.15 K were measured. Their standard enthalpies of formation were obtained, and the results were in order with −(1714.4 ± 3.2) kJ·mol −1 , −(1533.6 ± 3.3) kJ·mol −1 , −(697.8 ± 3.1) kJ·mol −1 , −(2418.9 ± 6.1) kJ·mol −1 , −(1134.8 ± 3.2) kJ·mol −1 , −(563.5 ± 3.2) kJ·mol −1 and −(966.2 ± 3.3) kJ·mol −1 , respectively.

研究领域: 物理化学 · 无机化学 · 热力学
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