首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Latent Porosity in Alkali-Metal M2B12F12 Salts: Structures and Rapid Room-Temperature Hydration/Dehydration Cycles
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Latent Porosity in Alkali-Metal M2B12F12 Salts: Structures and Rapid Room-Temperature Hydration/Dehydration Cycles

机译:碱金属M2B12F12盐中潜伏孔隙率:结构和快速室温水合/脱水循环

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摘要

Structures of the alkali-metal hydrates Li-2(H2O)(4)Z, LiK(H2O)(4)Z, Na-2(H2O)(3)Z, and Rb-2(H2O)(2)Z, unit cell parameters for Rb(2)Z and Rb-2(H2O)(2)Z, and the density functional theory (DFT)-optimized structures of K(2)Z, K-2(H2O)(2)Z, Rb(2)Z, Rb-2(H2O)(2)Z, Cs(2)Z, and Cs-2(H2O)Z are reported (Z(2-) = B12F122-) and compared with previously reported X-ray structures of Na-2(H2O)(0,4)Z, K-2(H2O)(0,2,4)Z, and Cs-2(H2O)Z. Unusually rapid room temperature hydration/dehydration cycles of several M(2)Z/M-2(H2O)(n)Z salt hydrate pairs, which were studied by isothermal gravimetry, are also reported. Finely ground samples of K(2)Z, Rb(2)Z, and Cs(2)Z, which are not microporous, exhibited latent porosity by undergoing hydration at 24-25 degrees C in the presence of 18 Ton of H2O(g) to K-2(H2O)(2)Z, Rb-2(H2O)(2)Z, and Cs-2(H2O)Z in 18, 40, and 16 min, respectively. These hydrates were dehydrated at 24-25 degrees C in dry N-2 to the original anhydrous M(2)Z compounds in 61, 25, and 76 min, respectively (the exact times varied from sample to sample depending on the particle size). The hydrate Na-2(H2O)(2)Z also exhibited latent porosity by undergoing multiple 90 min cycles of hydration to Na-2(H2O)(3)Z and dehydration back to Na-2(H2O)(2)Z at 23 degrees C. For the K(2)Z, Rb(2)Z, and Cs(2)Z transformations, the maximum rate of hydration (rh(max)) decreased, and the absolute value of the maximum rate of dehydration (rd(max)) increased, as T increased. For K(2)Z <-> K-2(H2O)(2)Z hydration/dehydration cycles with the same sample, the ratio rh(max)/rd(max) decreased 26 times over 8.6 degrees C, from 3.7 at 23.4 degrees C to 0.14 at 32.0 degrees C. For Rb(2)Z <-> Rb-2(H2O)(2)Z cycles, rh(max)/rd(max) decreased from 0.88 at 23 degrees C to 0.23 at 27 degrees C. For Cs(2)Z <-> Cs-2(H2O)Z cycles, rhmaird, decreased 20 times over 8 degrees C, from 6.7 at 24 degrees C to 0.34 at 32 degrees C. In addition, the reversible substitution of D2O for H2O in fully hydrated Rb-2(H2O)(2)Z in the presence of N-2/16 Torr of D2O(g) was complete in only 60 min at 23 degrees C.
机译:碱金属的结构水合物锂2(H2O)(4)Z,LIK(H2O)(4)Z,钠2(H2O)(3)Z,和R b-2(H2O)(2)Z,对于RB晶胞参数(2)Z和Rb-2(H2O)(2)Z,和密度泛函理论(DFT)K - 优化的结构(2)Z,K-2(H2O)(2)Z, RB(2)Z中,R b-2(H2O)(2)Z,CS(2)Z,和CS-2(H2O)Z的报道(Z(2-)= B12F122-)和与先前报告的X-相比的Na-2(H2O)(0,4)Z,K-2(H2O)(0,2,4)Z,和CS-2(H2O)z的射线结构。该研究通过等温重量分析异常快速室温水合/数M的脱水循环(2)Z / M-2(H2O)(N)z盐水合物对,也报道。其不是微孔K(2)Z中,R b(2)Z,和Cs(2)Z,磨细的样品,通过在H 2 O的18吨的存在下,在24-25度经历水合C(克发挥潜孔隙率),以K-2(H2O)(2)Z,RB-2(H2O)(2)Z,并在18 CS-2(H 2 O)Z,40,和16分别分钟,。这些水合物脱水在24-25摄氏度的无水N-2到原来的无水M(2)在61Ž化合物,25,和76分钟,分别为(改变从样品到样品的确切时间取决于粒径) 。水合物的Na-2(H2O)(2)Z也通过经历水合的多个90个分钟周期的Na-2(H2O)(3)Z和脱水回的Na-2(H2O)(2)Z在表现潜伏性的孔隙率23度C.对于K(2)Z中,R b(2)Z,和Cs(2)Z变换,(RH(最大))降低水合的最大速率,和脱水的最大速率的绝对值( RD(最大值))增加,为T增加。对于K(2)Z < - > K-2(H2O)(2)Z水合/用相同的样品脱水周期中,比Rh(最大值)/ RD(最大)超过8.6摄氏度在降低26倍,从3.7 23.4摄氏度到0.14在32.0℃下为RB(2)Z < - > RB-2(H2O)(2)Z周期,RH(最大)/ RD(最大)从0.88下降在23摄氏度至0.23在27度C.对于CS(2)Z < - > CS-2(H2O)z周期,rhmaird,超过8摄氏度在24摄氏度,在32摄氏度另外降低20倍,从6.7到0.34,可逆为H 2 O中充分D2O取代水合的Rb-2(H2O)(2)Z在存在的N- 2/16 D 2 O(克)的托在仅60分钟完成,在23℃下

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