Efficient construction of calcium fluoride nanoaggregates for enhanced water vapor adsorption

Calcium fluoride(CaF_(2))is an ideal adsorbent for the dehydration of gaseous hydrogen fluoride(HF)containing water vapor.In this work,a novel CaF_(2)absorbent,spherical CaF_(2)nanoaggregates(NAs)with a closely packed structure,was proposed and efficiently fabricated by spray drying technology.As the building blocks of CaF_(2)NAs,the CaF_(2)nanoparticles(NPs)were prepared by the addition of excess calcium ions(Ca^(2+))or fluorine ions(F−)in the synthesis.The results indicated that the CaF_(2)NPs synthesized by excess Ca^(2+)and the corresponding NAs exhibited much better water vapor adsorption properties than their counterparts by excess F−,owing to higher zeta potentials.More importantly,whether excess Ca^(2+)or F^(−),CaF_(2)NAs had further enhanced water vapor adsorption capacity compared to primary CaF_(2)NPs,possibly owing to their unique nano-micro secondary structures and higher surface areas.This work has great potential in the development of high-performance absorbents for separating moisture from corrosive gas HF.

Water adsorption performance of UiO-66 modified by MgCl_(2) for heat transformation applications

UiO-66 is a potential material for adsorption heat transformation(AHT)with high specific surface area,and excellent thermal and chemical stability.However,the low water adsorption capacity of UiO-66 in the low relative pressure range(0<P/P_(0)<0.3)limits its application in AHT.We prepare the UiO-66 modified by MgCl_(2)through using the solvothermal method and impregnation method,and study their water vapor adsorption performances and heat storage capacities.Attributed to the extremely high saturated water uptake and excellent hydrophilicity of MgCl_(2),the water adsorption performance of UiO-66 is improved,although the introduction of MgCl_(2)reduces its specific surface area and pore volume.The water adsorption capacity at P/P_(0)=0.3 and the saturated water adsorption capacity of the UiO-66(with MgCl_(2)content of 0.57 wt%)modified by the solvothermal method are 0.27 g/g and 0.57 g/g at 298 K,respectively,which are 68.8%and 32.6%higher than the counterparts of pure UiO-66,respectively.Comparing with pure UiO-66,the water adsorption capacity of the UiO-66(with MgCl_(2)content of 1.02 wt%)modified by the impregnation method is increased by 56.3%and 14.0%at the same pressure,respectively.During 20 water adsorption/desorption cycles,the above two materials show high heat storage densities(~1293 J/g and 1378 J/g).Therein,the UiO-66 modified by the solvothermal method exhibits the excellent cyclic stability.These results suggest that the introduction of an appropriate amount of MgCl_(2)makes UiO-66more suitable for AHT applications.

Modeling Water Adsorption and Retention of Building Materials From Pore Size Distribution

Water adsorption and capillarity are key phenomena involved during heat and moisture transfer in porous building materials.They account for interaction between solid matrix,liquid water and moist air.They are considered through Water Vapor Adsorption Isotherm(WVAI)and Retention Curve(RC)functions which are constitutive laws characterizing water activity within a porous medium.The objective of this paper is to present a water vapor adsorption and retention models built from multimodal Pore Size Distribution Function(PSDF)and to see how its parameters modify moisture storage for hygroscopic and near saturation ranges.The microstructure of the porous medium is represented statistically by a bundle of tortuous parallel pores through its PSDF.Firstly,the influence of contact angle and temperature on storage properties were investigated.Secondly,a parametric study was performed to see the influence of the PSDF shape on storage properties.Three cases were studied considering the number of modalities,the weight of each modality and the dispersion around mean radius.Finally,as a validation,the proposed model for WVAI were compared to existing model from literature showing a good agreement.This study showed that the proposed models are capable to reproduce various shapes of storage functions.It also highlighted the link between microstructure and adsorption-retention phenomena.

Analysis of trace mercury in water by solid phase extraction using dithizone modified nanometer titanium dioxide and cold vapor atomic absorption spectrometry

A new method for analysis of trace mercury in water samples was developed, based on the combination of preconcentration/separation using dithizone-modified nanometer titanium dioxide （TiO2） as a solid phase extractant and determination by cold vapor atomic adsorption spectrometry （CVAAS）. Dithizone was dissolved with alcohol and loaded on the surface of nano-sized TiO2 powders by stirring. The static adsorption behavior of Hg^2＋on the dithizone-modified nanoparficles was investigated in detail. It was found that excellent adsorption ratio for Hg^2＋ could be obtained in the pH range of 7-8 with an oscillation time of 15 rain, and a 5 mL of 3.5 mol·L^-1 HCI solution could quantitatively elute Hg^2＋ from nanometer TiO2 powder. Common coexisting ions caused no obvious influence on the determination of mercury. The mechanisms for the adsorption and desorption were discussed. The detection limit （30） for Hg^2＋ was calculated to be 5 ng·L^-1. The proposed method was applied to the determination of Hg^2＋ in a mineral water sample and a Zhujiang River water sample. By the standard addition method, the average recoveries were found to be 94.4%-108.3% with RSD （n = 5） of 2.9%-3.5%.

Pore-scale mechanisms and characterization of light oil storage in shale nanopores:New method and insights

A new method is proposed to analyze the pore-scale mechanisms and characterization of light oil storage in shale nanopores,which is based on the Hydrocarbon Vapor Adsorption(HVA)and Pore Calculation Model(PCM).First,the basic principle of the HVA-PCM method is introduced,and the experimental/mathematical analysis processes are given.Then,the HVA-PCM method is applied to shale samples to analyze the mechanisms and characterization of light oil storage in shale nanopores.The results provide insights into the pore-scale oil storage mechanisms,oil storage structure,oil film thickness,oil distribution within different sized pores,and the oil storage state.Finally,the advantages and limitations of the HVA-PCM method are discussed,and suggestions for further improvement are proposed.Overall,the HVA-PCM method is a powerful tool for extracting quantitative information on the light oil storage in shale nanopores.

A series of high-nuclear planar equilateral triangle-shaped {Ln_(6)(μ_(3)-OH)_(6)} cluster encapsulated polyoxoniobates with frequency dependent magnetic property

The integration of lanthanide(Ln)ions and polyoxoniobates(PONbs)is challenging,and the know Ln-substituted PONbs are still scarce.This work introduces high-nuclear iso-Ln-oxo clusters into th PONb system.The first series of high-nuclear Ln-oxo clusters encapsulated heterometallic polyoxonio bates H_9[Na(H_(2)O)_(4)][Cu(en)_(2)]_(10){Ln_6(μ_(3)-OH)_6(Si Nb_(18)O_(54))_(3)}·18H_(2)O(1-Ln,en=ethylenediamine,Ln=Dy,Gd Tb,Ho,Er,Tm,Yb,Lu)based on flower-like{Ln_(6)(μ_(3)-OH)_(6)(Si Nb_(18)O_(54))_(3)}({Ln_6Si_(3)Nb_(54)})clusters hav been successfully synthesized via one-pot hydrothermal synthesis strategy.The flower-like polyoxoanio{Ln_6Si_(3)Nb_(54)}is consisted of three heteropolyoxoniobate{Si Nb_(18)O_(54)}clusters and one unique planar equ lateral triangle-shaped{Ln_6(μ_(3)-OH)_6}cluster,which presents the highest nuclear iso-Ln-oxo cluster i PONb chemistry.In{Ln_6(μ_(3)-OH)_6}cluster,each pair ofμ_(3)-OH groups link three Dy^(3+)ions to form a sma approximate equilateral triangle-shaped{Dy_(3)(OH)_(2)}cluster.Furthermore,the three{Dy_(3)(OH)_(2)}cluster comprise a bigger approximate equilateral triangle-shaped{Dy_6(μ_(3)-OH)_6}cluster.The reported hexanu clear{Ln_6}cluster skeletons are mostly octahedral,however,such equilateral triangle-shaped skeleton o the hexanuclear Ln-oxo cluster is first observed.The 1-Dy exhibits good water vapor adsorption capacit and ferromagnetic properties.

Synthesis of porous aromatic framework with Friedel–Crafts alkylation reaction for CO_2 separation

A novel porous aromatic framework, PAF-8, derived from tetraphenylsilane as basic building unit, was successfully synthesized via Friedel-Crafts alkylation reaction. This PAF material had high thermal stability as well as high surface area （785 m^2 g^-1） calculated from the Brunauer-Emmett-Teller （BET） model. Meanwhile, PAF-8 possessed high performances in gas sorption and especially for CO2 separation.