Cetyltrimethylammonium Bromide PAGE and Eastern Blotting

2021 ◽  
pp. 243-256
Author(s):  
Biji T. Kurien
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
Eastern Blotting

New Structure of CTAB Templated Silica Films as revealed by GISAXS coupled to HRTEM

2000 ◽  
Vol 628 ◽  
Author(s):  
Sophie Besson ◽  
Catherine Jacquiod ◽  
Thierry Gacoin ◽  
André Naudon ◽  
Christian Ricolleau ◽  
...  
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
Grazing Incidence ◽  
Hexagonal Structure ◽  
X Ray Diffraction ◽  
Electronic Microscopy ◽  
Silica Films ◽  
X Ray ◽  
X Ray Scattering ◽  
Hexagonal Arrangement ◽  
Spherical Micelles

ABSTRACTA microstructural study on surfactant templated silica films is performed by coupling traditional X-Ray Diffraction (XRD) and Transmission Electronic Microscopy (TEM) to Grazing Incidence Small Angle X-Ray Scattering (GISAXS). By this method it is shown that spin-coating of silicate solutions with cationic surfactant cetyltrimethylammonium bromide (CTAB) as a templating agent provides 3D hexagonal structure (space group P63/mmc) that is no longer compatible with the often described hexagonal arrangement of tubular micelles but rather with an hexagonal arrangement of spherical micelles. The extent of the hexagonal ordering and the texture can be optimized in films by varying the composition of the solution.

Effect of cetyltrimethylammonium bromide on the electrochemiluminiscence and electrooxidation of luminol

1983 ◽  
Vol 48 (2) ◽  
pp. 477-483 ◽  
Author(s):  
Jan Lasovský ◽  
František Grambal
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
Linear Sweep Voltammetry ◽  
Critical Micellar Concentration ◽  
Peak Height ◽  
Anodic Peak ◽  
Alkaline Solutions ◽  
Platinum Electrodes ◽  
Micellar Solutions ◽  
Linear Sweep ◽  
Low Concentrations

The electrooxidation of luminol in alkaline solutions in the presence of cetyltrimethylammonium bromide (I) was studied by linear sweep voltammetry on fixed and vibrating platinum electrodes. The presence of I in low concentrations (below the critical micellar concentration) brings about aggregation of the luminol, which is manifested by an increase in the anodic peak height and its shift towards lower potentials. In micellar solutions the peak height decreases owing to the slower diffusion of the bulkier micelles, the shift to lower potentials being preserved. The light-voltage curves correspond with the voltammetric curves, exhibiting identical shifts of the peak potentials in dependence on the concentration of the surfactant.

Electrochemical Production of Formic Acid from CO 2 with Cetyltrimethylammonium Bromide‐Assisted Copper‐Based Catalysts

ChemSusChem ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 1962-1969
Author(s):  
Yanling Qiu ◽  
Wenbin Xu ◽  
Pengfei Yao ◽  
Qiong Zheng ◽  
Huamin Zhang ◽  
...  
Keyword(s):  
Formic Acid ◽  
Cetyltrimethylammonium Bromide ◽  
Electrochemical Production

scholarly journals Offretite Zeolite Single Crystals Synthesized by Amphiphile-Templating Approach

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2238
Author(s):  
Eng-Poh Ng ◽  
Nur Hidayahni Ahmad ◽  
Fitri Khoerunnisa ◽  
Svetlana Mintova ◽  
Tau Chuan Ling ◽  
...  
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
Cost Effective ◽  
Acid Sites ◽  
Biofuel Production ◽  
Structure Directing Agent ◽  
High Crystallinity ◽  
Organic Templates ◽  
Synthesis Approach ◽  
Conventional Counterpart ◽  
Dual Functions

Offretite zeolite synthesis in the presence of cetyltrimethylammonium bromide (CTABr) is reported. The offretite crystals were synthesized with a high crystallinity and hexagonal prismatic shape after only 72 h of hydrothermal treatment at 180 °C. The CTABr has dual-functions during the crystallization of offretite, viz. as structure-directing agent and as mesoporogen. The resulting offretite crystals, with a Si/Al ratio of 4.1, possess more acid sites than the conventional offretite due to their high crystallinity and hierarchical structure. The synthesized offretite is also more reactive than its conventional counterpart in the acylation of 2-methylfuran for biofuel production under non-microwave instant heating condition, giving 83.5% conversion with 100% selectivity to the desired product 2-acetyl-5-methylfuran. Hence, this amphiphile synthesis approach offers another cost-effective and alternative route for crystallizing zeolite materials that require expensive organic templates.

scholarly journals Phytotoxicity of Silver Nanoparticles on Tobacco Plants: Evaluation of Coating Effects on Photosynthetic Performance and Chloroplast Ultrastructure

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 744
Author(s):  
Petra Peharec Štefanić ◽  
Karla Košpić ◽  
Daniel Mark Lyons ◽  
Lara Jurković ◽  
Biljana Balen ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Cetyltrimethylammonium Bromide ◽  
Photosynthetic Apparatus ◽  
Chloroplast Ultrastructure ◽  
Photosynthetic Performance ◽  
Pigment Content ◽  
Inhibitory Effects ◽  
Tobacco Plants ◽  
Agriculture And Food ◽  
The Impact

Silver nanoparticles (AgNPs) are the most exploited nanomaterial in agriculture and food production, and their release into the environment raises concern about their impact on plants. Since AgNPs are prone to biotransformation, various surface coatings are used to enhance their stability, which may modulate AgNP-imposed toxic effects. In this study, the impact of AgNPs stabilized with different coatings (citrate, polyvinylpyrrolidone (PVP), and cetyltrimethylammonium bromide (CTAB)) and AgNO3 on photosynthesis of tobacco plants as well as AgNP stability in exposure medium have been investigated. Obtained results revealed that AgNP-citrate induced the least effects on chlorophyll a fluorescence parameters and pigment content, which could be ascribed to their fast agglomeration in the exposure medium and consequently weak uptake. The impact of AgNP-PVP and AgNP-CTAB was more severe, inducing a deterioration of photosynthetic activity along with reduced pigment content and alterations in chloroplast ultrastructure, which could be correlated to their higher stability, elevated Ag accumulation, and surface charge. In conclusion, intrinsic properties of AgNP coatings affect their stability and bioavailability in the biological medium, thereby indirectly contributing changes in the photosynthetic apparatus. Moreover, AgNP treatments exhibited more severe inhibitory effects compared to AgNO3, which indicates that the impact on photosynthesis is dependent on the form of Ag.

Interaction of sulphone based reactive dyes with cationic surfactant: a spectroscopic and conductometric study

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Misbah Iram ◽  
Hamadia Sultana ◽  
Muhammad Usman ◽  
Bazgha Ahmad ◽  
Nadia Akram ◽  
...  
Keyword(s):  
Strong Interaction ◽  
Cetyltrimethylammonium Bromide ◽  
Hydrophobic Interactions ◽  
Reactive Dyes ◽  
Micellar System ◽  
Palisade Layer ◽  
Micellar Systems ◽  
Gibbs Energies ◽  
Electrostatic And Hydrophobic Interactions ◽  
Conductometric Study

Abstract Interaction of sulphone based reactive dyes, designated as dye-1 and dye-2, with cationic micellar system of cetyltrimethylammonium bromide (CTAB), has been investigated by spectroscopic and conductometeric measurements. Efficiency of the selected micellar systems is assessed by the values of binding constant (K b ), partition coefficient (K x ) and respective Gibbs energies. Critical micelle concentration (CMC) of surfactant, electrostatic and hydrophobic interactions as well as polarity of the medium plays significant role in this phenomenon. The negative values of Gibbs energies of binding (∆G b ) and partition (∆G p ) predicts the feasibility and spontaneity of respective processes. Similarly negative values of ∆G m and ∆H m and positive values of ∆S m , calculated from conductometeric data, further, revealed the exothermicity, spontaneity and, thus, stability of system. The results, herein, have disclosed the strong interaction between dye and surfactant molecules. The dye-2 has been observed to be solubilized to greater extent, as compared to dye 1, due to strong interaction ith hydrophiles of CTAB and accommodation of its molecules in palisade layer of micelle closer to the micelle/water interface.

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