scholarly journals Solid-state synthesis and physico-chemical characterization of modified smectites using natural clays from Burkina Faso

2021 ◽  
Vol 35 (1) ◽  
pp. 43-59
Author(s):  
I. Garikoé ◽  
B. Sorgho ◽  
B. Guel ◽  
I. Persson
Keyword(s):  
Solid State ◽  
Burkina Faso ◽  
Chemical Characterization ◽  
Textural Properties ◽  
Exchange Capacity ◽  
Basal Spacing ◽  
Hexadecyltrimethylammonium Bromide ◽  
Tetradecyltrimethylammonium Bromide ◽  
Low Concentrations ◽  
Natural Clays

Solid-state intercalation was applied to prepare organo-smectites using cationic surfactants and natural clays containing smectite at various surfactant/smectite ratios. The surfactants enter the interlayers of smectites causing a swelling of the clays. The used clays were collected in Siétougou and Diabari villages located in the eastern part of Burkina Faso. The solid-state intercalation was successful for all four surfactants applied, n-dodecyltrimethylammonium bromide, (n-C12H25(CH3)3NBr), n-tetradecyltrimethylammonium bromide, (n-C14H29(CH3)3NBr), n-hexadecyltrimethylammonium bromide (n-C16H33(CH3)3NBr) and di-n-dodecyldimethyl­ammonium bromide ((n-C12H25)2(CH3)2NBr) at different levels of the cation exchange capacity (CEC). The synthesized organo-smectites were characterized regarding relative density, structural and textural properties. XRPD data showed a systematic increase of the basal spacing of the unit cell of the smectite up to >38 Å at 2.0-CEC loading of the surfactant. This increase indicates that the surfactants penetrated into the smectite interlayers with the surfactants being arranged parallel to the layers at low concentrations and almost perpendicular at high ones. FTIR spectra of the organo-smectites showed a decrease in the intensities of the water bands at around 1630 cm-1 and 3400 cm-1, and new specific bands close to 2920 cm-1 and 2850 cm-1 were assigned to the asymmetric and symmetric stretching of CH2 groups of the surfactants, respectively.                     KEY WORDS: Smectite, Organo-smectite, Surfactant, Intercalation   Bull. Chem. Soc. Ethiop. 2021, 35(1), 43-59. DOI: https://dx.doi.org/10.4314/bcse.v35i1.4

scholarly journals Submicellar complexes may initiate the fungicidal effects of cationic amphiphilic compounds on Candida albicans.

1997 ◽  
Vol 41 (3) ◽  
pp. 544-550 ◽  
Author(s):  
B Ahlström ◽  
M Chelminska-Bertilsson ◽  
R A Thompson ◽  
L Edebo
Keyword(s):  
Candida Albicans ◽  
Membrane Damage ◽  
Hydrocarbon Chain ◽  
Hexadecyltrimethylammonium Bromide ◽  
Tetradecyltrimethylammonium Bromide ◽  
Low Concentrations ◽  
Hydrocarbon Chains ◽  
Absorbing Material ◽  
High Concentrations ◽  
Chain Lengths

The killing of Candida albicans by a series of amphiphilic quaternary ammonium compounds (QACs) with different hydrocarbon chain lengths was closely related to the binding of the compounds to the cells and damage of the cell membranes. The membrane damage was measured as the level of release of the UV-absorbing material into the medium in which the cells were suspended and as the level of uptake of propidium iodide in individual cells by flow cytometry. It was shown that of the compounds tested, hexadecyltrimethylammonium bromide (cetyltrimethylammonium bromide [CTAB]) bound most efficiently. Tetradecyl betainate chloride (B14), tetradecanoylcholine bromide (C14), tetradecyltrimethylammonium bromide (TTAB), and dodecyltrimethylammonium bromide (DTAB) followed and had declining degrees of binding efficiency. The proportion of CTAB bound was almost total at concentrations up to the critical micelle concentration (CMC) of the compound, whereas that of B14 was somewhat smaller. For the two remaining tetradecyl compounds (C14 and TTAB), still smaller proportions were bound at low concentrations, but the proportions rose disproportionally at increasing concentrations to a distinct maximum at concentrations of 0.2 to 0.5 times the CMC. We propose that interfacial micelle-like aggregates are formed at the cell surface as a step in the binding process. An analogous, but less conspicuous, maximum was seen for DTAB. Thus, great differences in the binding affinity of QACs with different hydrocarbon chains at different concentrations to C. albicans were observed. These differences were related to the CMC of the compound. In contrast, the binding of TTAB to Salmonella typhimurium 395 MS was almost total at low as well as high concentrations until saturation was attained, indicating fundamental differences between binding to the yeast and binding to gram-negative bacteria. The importance of lipid-type complexes or aggregates to the antifungal effect of membrane-active substances are discussed.

scholarly journals Characterisation of Natural and HDTMA-Br Modified Dijah-Monkin Bentonite Clay: FTIR, XRF, XRD and SEM

2021 ◽  
Vol 7 (5) ◽  
pp. 2010-2018
Author(s):  
Olukayode Gideon Oloyede ◽  
◽  
Umar Omeiza Aroke ◽  
Saidat Olanipekun Giwa ◽  
Alexander Asanja Jock ◽  
...  
Keyword(s):  
Cation Exchange Capacity ◽  
Bentonite Clay ◽  
Exchange Capacity ◽  
Basal Spacing ◽  
Hexadecyltrimethylammonium Bromide ◽  
Acid Activation ◽  
X Ray Diffraction ◽  
X Ray ◽  
North East ◽  
Scanning Electron

In this study, Dijah-Monkin bentonite clay was modified with a cationic surfactant hexadecyltrimethylammonium bromide (HDTMA-Br) at the level of twice the cation exchange capacity (CEC). This process results in the development of hydrophobic organoclay with an improved adsorption capacity. The clay obtained from Zing LGA Taraba State, North-East Nigeria, was beneficiated and pulverised to a particle size of 125 µm. The modification was performed without acid activation to prevent damages to the clay’s crystal structure. The organoclay was characterised for chemical composition, functional groups, mineralogical and surface morphology using X-ray fluorescence (XRF), Fourier Transform Infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The XRD showed an increase in the basal spacing from 15.681Å to 17.758 Å, while the XRF revealed a 5.35% concentration of Br on the modified clay, indicating successful intercalation. The FTIR spectra also revealed the appearance of symmetric and asymmetric stretching bands at 2847.7cm-1 and 2914.8cm-1, respectively, as a consequence of the modification, resulting in more sites for adsorption.

scholarly journals Rheological and Textural Properties of Apple Pectin-Based Composite Formula with Xanthan Gum Modification for Preparation of Thickened Matrices with Dysphagia-Friendly Potential

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 873
Author(s):  
Huaiwen Yang ◽  
Chai-Chun Tsai ◽  
Jung-Shiun Jiang ◽  
Chi-Chung Hua
Keyword(s):  
Storage Modulus ◽  
Water Consumption ◽  
Xanthan Gum ◽  
Loss Modulus ◽  
Textural Properties ◽  
Apple Pectin ◽  
Composite Matrix ◽  
Low Concentrations ◽  
Composite Formula

Modifying the consistency of a given edible fluid matrix by incorporating food thickeners is a common nursing remedy for individuals with dysphagia when adequate water consumption is a concern. As apple pectin (AP) offers nutraceutical benefits, properly formulated apple pectin (AP)-based thickeners featuring xanthan gum (XG) can be superior candidates for preparation of dysphagia-friendly matrices (DFMs). Our recruited DFMs exhibit fluid-like behavior (loss modulus > storage modulus, G” > G’) at lower AP concentrations (2 and 5%, w/w); they turn into weak/critical gels (G’ ≈ G”) as the concentration becomes higher (9%). In contrast, XG-DFMs display gel-like attributes with G’ > G”, even at rather low concentrations (<1%) and become more resistant to sugar, Na+, and Ca2+ modifications. The composite matrix of AP1.8XG0.2 (constraint at 2%) exhibits a confined viscosity of 278 ± 11.7 mPa∙s, which is considered a DFM, in comparison to only AP- or XG-thickened ones. The hardness measurements of XG0.6 and AP1.2XG0.8 are 288.33 ± 7.506 and 302.00 ± 9.849 N/m2, respectively, which potentially represent a promising formulation base for future applications with DFMs; these textural values are not significantly different from a commercially available product (p > 0.05) for dysphagia nursing administrations.

scholarly journals Physico-Chemical Characterization and Antimicrobial Properties of Hybrid Film Based on Saponite and Phloxine B

Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 325
Author(s):  
Nitin Chandra teja Dadi ◽  
Matúš Dohál ◽  
Veronika Medvecká ◽  
Juraj Bujdák ◽  
Kamila Koči ◽  
...  
Keyword(s):  
Hybrid Film ◽  
Antimicrobial Properties ◽  
Chemical Characterization ◽  
Layered Silicate ◽  
Contact Angles ◽  
Exchange Capacity ◽  
Resistant Bacteria ◽  
Hybrid Films ◽  
Water Contact ◽  
Physico Chemical

This research was aimed at the preparation of a hybrid film based on a layered silicate saponite (Sap) with the immobilized photosensitizer phloxine B (PhB). Sap was selected because of its high cation exchange capacity, ability to exfoliate into nanolayers, and to modify different surfaces. The X-ray diffraction of the films confirmed the intercalation of both the surfactant and PhB molecules in the Sap film. The photosensitizer retained its photoactivity in the hybrid films, as shown by fluorescence spectra measurements. The water contact angles and the measurement of surface free energy demonstrated the hydrophilic nature of the hybrid films. Antimicrobial effectiveness, assessed by the photodynamic inactivation on hybrid films, was tested against a standard strain and against methicillin-resistant bacteria of Staphylococcus aureus (MRSA). One group of samples was irradiated (green LED light; 2.5 h) and compared to nonirradiated ones. S. aureus strains manifested a reduction in growth from 1-log10 to over 3-log10 compared to the control samples with Sap only, and defects in S. aureus cells were proven by scanning electron microscopy. The results proved the optimal photo-physical properties and anti-MRSA potential of this newly designed hybrid system that reflects recent progress in the modification of surfaces for various medical applications.

scholarly journals Mineralogical characterization of natural clays from Brazilian Southeast region for industrial applications

Cerâmica ◽  
2017 ◽  
Vol 63 (366) ◽  
pp. 253-262 ◽  
Author(s):  
N. I. Alvarez Acevedo ◽  
M. C. G. Rocha ◽  
L. C. Bertolino
Keyword(s):  
Specific Surface ◽  
Clay Fraction ◽  
Exchange Capacity ◽  
Size Analysis ◽  
Mineralogical Characterization ◽  
Southeast Region ◽  
Pore Size Analysis ◽  
Two Samples ◽  
Natural Clays ◽  
Cationic Exchange

Abstract Characterization studies of clays are often performed to identify possible markets for these materials. Bearing this in mind, two samples of natural clays from the Southeast region of Brazil were studied. Conventional techniques of characterization were used. Granulometric analysis and determination of cationic exchange capacity of these clays were also performed. Nitrogen adsorption-desorption measurements were used to determine the Brunauer-Emmett-Teller specific surface area, and Barrett-Joyner-Halenda and t-plot pore size analysis were carried out. The results obtained were similar for the two clays. Both present high clay fraction (above 80 wt%) composed of illite, kaolinite and quartz minerals. Stratified illite-smectite structures were also observed. Traces of calcite were detected in one of the clay samples, while traces of montmorillonite were observed in the other sample. These results were corroborated by the low cationic exchange capacity values obtained for both clays. These clays showed good adsorptive properties, evidenced by their specific surface areas, with predominantly mesoporous structures and slit-like pores. According to their features, these clays have potential use as adsorbents to replace more expensive materials due to their easy availability and low cost.

scholarly journals Investigation of activated Al-pillared clay efficiency in vegetable oil purification

2004 ◽  
pp. 31-36 ◽  
Author(s):  
Gizela Lomic ◽  
Erne Kis ◽  
Etelka Dimic ◽  
Ranko Romanic
Keyword(s):  
Surface Area ◽  
Vegetable Oil ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Sample Surface ◽  
Pillared Clay ◽  
Acid Activation ◽  
Micropore Surface Area ◽  
Natural Clays ◽  
Oil Purification

This paper represents a contribution to the applicability of natural clays and their derivates as adsorbents in the process of purification of vegetable oil. Investigation of textural properties of raw and purified clay samples reveals that during acid activation and Al-pillaring, BET and micropore surface area increases significantly. However, bleaching capacity of clay and its derivates is not determined by using sample surface area, but rather sample total pore volume. Surface area, especially micropore surface area contributes to removal of smaller molecules. This was confirmed by successful elimination of moisture and volatile materials by samples with an appropriate micropore structure. Used samples of clay and its derivates do not significantly influence acid and peroxide values of raw sunflower oil during its treatment.

Physico-Chemical Characterization of Drugs and Drug Forms in the Solid State

ChemInform ◽  
2004 ◽  
Vol 35 (25) ◽  
Author(s):  
A. Marini ◽  
V. Berbenni ◽  
G. Bruni ◽  
P. Cofrancesco ◽  
F. Giordano ◽  
...  
Keyword(s):  
Solid State ◽  
Chemical Characterization ◽  
Physico Chemical

scholarly journals Mineralogical and Chemical Characterization of Zr-REE-Nb Ores from Khalzan Buregtei (Mongolia)—Approaches to More Efficient Extraction of Rare Metals from Alkaline Granitoids

Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 217 ◽  
Author(s):  
Lars Hans Gronen ◽  
Sven Sindern ◽  
Janet Lucja Katzmarzyk ◽  
Udo Bormann ◽  
André Hellmann ◽  
...  
Keyword(s):  
Size Fraction ◽  
Chemical Characterization ◽  
Textural Properties ◽  
Rare Metal ◽  
Ore Minerals ◽  
Deposit Type ◽  
Energy Consuming ◽  
Automated Mineralogy ◽  
Efficient Extraction ◽  
Rock Suite

Alkaline rocks are worldwide observed as hosts for rare metal (Zr-REE-Nb) minerals. The classification of the ore bearing rock type is challenging due to the fact that textures and mineral assemblage are obscured by post-magmatic alteration. In addition, the alteration causes fine and intricate intergrowth of the ore minerals with associated gangue. Hence, intensive comminution is necessary to liberate the ore minerals, which is one parameter hampering the economical use of this deposit type. This study provides a quantitative mineralogical investigation of the ore bearing rock suite at Khalzan Buregtei as an example of rare metal deposits. R1-R2 multication parameters are shown to be highly appropriate as quantitative mineralogical indicators based on readily available major element datasets to visualize and quantify alteration types of the ore bearing rock suite. The ore minerals were found to be associated with a cluster-forming assemblage of post-magmatic phases. Automated mineralogy was applied to quantify the textural properties of the ore mineral clusters. This finding permits efficient pre-concentration of rare metal ore at coarser particle size fraction, requiring less energy consuming comminution.

Cation exchange in synthetic manganates: II. The structure of an alkylammonium-saturated phyllomanganate

Clay Minerals ◽  
1986 ◽  
Vol 21 (5) ◽  
pp. 957-964 ◽  
Author(s):  
E. Paterson ◽  
D.R. Clark ◽  
D. Russell ◽  
R. Swaffield
Keyword(s):  
Chain Length ◽  
Photoelectron Spectroscopy ◽  
Hydrocarbon Chain ◽  
Exchange Capacity ◽  
Basal Spacing ◽  
Water Molecules ◽  
Interlayer Water ◽  
X Ray ◽  
Alkyl Chains ◽  
Hydrocarbon Chain Length

AbstractA synthetic phyllomanganate saturated with a series of primary alkylammonium cations has been examined using XRD, chemical analysis and X-ray photoelectron spectroscopy. A linear relationship exists between the basal spacing of the saturated alkylammonium-manganate and the hydrocarbon chain length in the interlayer, and from the gradient it is concluded that the alkyl chains are perpendicular to the manganate sheet. This orientation is a function of both the charge density and the presence of a layer of water molecules immediately adjacent to the manganate basal surfaces. Evacuation results in the loss of this interlayer water and the structure of the organo-manganate is considerably disrupted. The extent to which the interlayer arrangement can be reinstated by rehydration is dependent on the chain length of the saturating organo-cation. For cations of chain length > C6 the C contents suggest that cation in excess of the exchange capacity is present in the interlayer, but the absence of any compensating anion and the release of amine on evacuation suggests that the excess C arises from the presence of free amine.

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