Characterization of organo-kenyaites: thermal stability and their effects on eosin removal characteristics

Clay Minerals ◽  
2018 ◽  
Vol 53 (1) ◽  
pp. 91-104 ◽  
Author(s):  
F. Kooli ◽  
Y. Liu ◽  
K. Hbaieb ◽  
O.Y. Ching ◽  
R. Al-Faze

ABSTRACTOrgano-kenyaites were prepared from a cetyltrimethylammonium hydroxide (C16TMAOH) solution and solid sodium kenyaite (Na2Si22O45.10H2O) mixture. The effect of the initial cetyltrimethylammonium solution on the structure of the intercalated materials was investigated by CHN analyses, X-ray diffraction (XRD), thermogravimetric analysis, SEM, and 29Si and 13C solid NMR techniques. For C16TMAOH concentration 0.25 mM, the Na+ cations were fully exchanged. Initial C16TMAOH concentrations higher than 0.25 mM had little effect on the intercalated amount of C16TMA+ cations. The organic cations content reached a plateau of 0.66 mmol/g. The arrangement model of C16TMA+ cations corresponded to a tilt of the organic cations to the silicate layers with an angle of 42° as deduced by XRD studies. The C16TMA+ cations exhibited mainly trans-configuration of the methyl chains, as was shown by solid 13C NMR. The thermal stability of the organo-silicates was studied using in situ FTIR and in situ XRD in the range 25–450°C. The C16TMA-kenyaites were stable at temperatures below 200°C. They collapsed at higher temperatures due to the decomposition of the intercalated surfactants. These organo-kenyaites were used to remove the acidic dye molecule, eosin. The removal tests were performed at varying conditions of initial dye concentrations, organic content in the organo-kenyaites and heating temperatures. In general, the organic modification improved the removal capacity of the Na-kenyaite from 2 mg of eosin/g to 60 mg of eosin/g, and this capacity was related to the organic contents and the calcination temperatures of the organo-kenyaites.

2018 ◽  
Vol 6 (24) ◽  
pp. 11496-11506 ◽  
Author(s):  
Paul Pistor ◽  
Thomas Burwig ◽  
Carlo Brzuska ◽  
Björn Weber ◽  
Wolfgang Fränzel

We present the identification of crystalline phases by in situ X-ray diffraction during growth and monitor the phase evolution during subsequent thermal treatment of CH3NH3PbX3 (X = I, Br, Cl) perovskite thin films.


2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Mashael Alshabanat ◽  
Amal Al-Arrash ◽  
Waffa Mekhamer

Polymer nanocomposites of polystyrene matrix containing 10% wt of organo-montmorillonite (organo-MMT) were prepared using the solution method with sonication times of 0.5, 1, 1.5, and 2 hours. Cetyltrimethylammonium bromide (CTAB) is used to modify the montmorillonite clay after saturating its surface with Na+ions. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to characterize the montmorillonite before and after modification by CTAB. The prepared nanocomposites were characterized using the same analysis methods. These results confirm the intercalation of PS in the interlamellar spaces of organo-MMT with a very small quantity of exfoliation of the silicate layers within the PS matrix of all samples at all studied times of sonication. The thermal stability of the nanocomposites was measured using thermogravimetric analysis (TGA). The results show clear improvement, and the effects of sonication time are noted.


2015 ◽  
Vol 88 (1) ◽  
pp. 138-146 ◽  
Author(s):  
Rouhollah Bagheri ◽  
Reza Darvishi

ABSTRACT In this study, polyurethane (PU)/organomodified montmorillonite (cloisite®30B) is synthesized via in situ polymerization by reaction of an ether-based prepolymer with the isocyanate end groups and adiamine chain extender (4, 4-methylene-bis(2-chloroaniline)) in the presence of different amounts of nanoparticles dispersed in the prepolymer matrix by an ultrasonic mixer for 1 h. The synthesized polymers are cast on a pretreated carbon steel sheet and cured at 120 °C in an oven. The PU and its composites have been characterized by using Fourier transform infrared spectroscopy, X-ray diffraction (XRD), and mechanical testing. The XRD analysis of the cured samples containing 1 to 3 wt% cloisite30B showed intercalation segments in the silicate layers and exfoliation for 0.5 wt% nanoparticles. The highest mechanical properties were obtained using the cured exfoliated silicate layer sample. A twofold increase in the ultimate tensile strength and a 2.3 times increase in the adhesion strength were found for 0.5 wt% organoclay/PU as compared with that of pure PU. In addition, the exfoliated structure sample exhibited a 16% reduction in abrasion compared with that of pure PU.


2016 ◽  
Vol 72 (a1) ◽  
pp. s418-s418 ◽  
Author(s):  
Claudia Cancellieri ◽  
Frank Moszner ◽  
Mirco Chiodi ◽  
Songhak Yoon ◽  
Daniel Ariosa ◽  
...  

2014 ◽  
Vol 904 ◽  
pp. 7-9
Author(s):  
Xiao Hua Gu ◽  
Xi Wei Zhang ◽  
Bao Yun Xu ◽  
Peng Zeng

In this paper, the diphenyl methane diisocyanate (MDI) was used to modify montmorillonoid (MMT) and got the organic montmorillonite (OMMT), which was used with the monomers of PET by in situ polymerization method to prepare PET/MMT nanocomposition. The OMMT was analyzed by the X ray diffraction (XRD) to test the change of the spacing layer. Dispersion of MMT in the PET/MMT nanocomposites were studied with XRD and SEM and by means of thermogravimetric analyzer (TGA) on the thermal stability of PET/MMT nanocomposites. The results showed that, MDI modified MMT successfully, and the compatibility of MMT and PET was increased .


Energies ◽  
2020 ◽  
Vol 13 (8) ◽  
pp. 1972
Author(s):  
Gyoung-Ja Lee ◽  
Min-Ku Lee

Temperature stability of dielectric, ferroelectric, and piezoelectric properties were investigated in situ by choosing (K,Na)NbO3-(Bi,K)ZrO3 (KNN-BKZ), (K,Na)NbO3-(Bi,Na,K,Li)ZrO3 (KNN-BNKLZ), and (K,Na)NbO3-(Bi,Li)ZrO3-(KNN-BLZ) as representative ceramics with rhombohedral-orthorhombic-tetragonal (R-O-T), R-T, and enriched T phase boundaries, respectively. The KNN-BNKLZ ceramics, which have an R-T phase boundary, showed the highest piezoelectricity but the worst temperature stability. On the other hand, the KNN-BLZ ceramics, which have an enriched T-phase, were slightly worse in terms of piezoelectricity compared to the R-O-T or R-T phase boundary, but their thermal stability was the best. From analyses of an extrinsic contribution by a difference between the small signal d33 and εrPr and an intensity variation of the (002) and (200) X-ray diffraction peaks for the KNN-based ceramics, it was suggested that increasing the extrinsic contribution in the morphotropic phase boundary region improves the piezoelectricity but decreases the thermal stability.


2020 ◽  
Vol 6 (13) ◽  
pp. eaaz3168 ◽  
Author(s):  
Martin-Louis Y. Riu ◽  
Rebecca L. Jones ◽  
Wesley J. Transue ◽  
Peter Müller ◽  
Christopher C. Cummins

This exploratory synthesis investigation was undertaken to determine the viability of replacing a single carbon vertex with another p-block element in a highly strained tetrahedrane molecule. Phosphorus was selected for this purpose because the stable molecular form of elemental phosphorus is tetrahedral. Our synthetic strategy was to generate an unsaturated phosphorus center bonded to a substituted cyclopropenyl group, a situation that could lead to closure to provide the desired phosphatetrahedrane framework. This was accomplished by dehydrofluorination of the in situ generated fluorophosphine H(F)P(CtBu)3. Tri-tert-butyl phosphatetrahedrane, P(CtBu)3, was then isolated in 19% yield as a low-melting, volatile, colorless solid and characterized spectroscopically and by a single-crystal x-ray diffraction study, confirming the tetrahedral nature of the molecule’s PC3 core. The molecule exhibits unexpected thermal stability.


2014 ◽  
Vol 915-916 ◽  
pp. 780-783
Author(s):  
Hong Wang ◽  
Ming Tian Li ◽  
Yue Lu ◽  
Di Liu

Pyrrole and m-toluidine copolymer (P(PY/MT)) / montmorillonite (MMT) Composites were prepared by in situ chemical polymerization of pyrrole with m-toluidine monomer in the presence of montmorillonite. The structural, morphological and thermal properties of these composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). X-ray diffraction result for P(PY/MT)-MMT illuminated the intercalation of P(PY/MT) copolymer between the clay layers. The FT-IR result showed the successful incorporation of montmorillonite clay in the prepared P(PY/MT)/MMT composite. The higher thermal stability of high MMT content rate might be attributed to its higher chain compactness due to the interfacial interaction between the P(PY/MT) and the clay.


Sign in / Sign up

Export Citation Format

Share Document