scholarly journals Thermal behaviour of different non-ionic surfactant concentration on the polymeric membrane

2021 ◽  
Vol 1874 (1) ◽  
pp. 012059
Author(s):  
B BadrulHaswan ◽  
A R Hassan ◽  
K Ali ◽  
A A M Redhwan ◽  
A Nasir
2014 ◽  
Vol 1044-1045 ◽  
pp. 344-347 ◽  
Author(s):  
De Shuai Sun ◽  
Long Fang ◽  
Ya Li Liu

Inhalable particles suspended in air were an important pollution of atmospheric Environment. Because of very small in size, they were different to be captured by conventional filter. Chemical active agent, surfactant and flocculate, were introduced into chamber and encouraged the agglomeration of inhalable particles. Nonionic surfactant could reduce more than 30% of particles, while ionic surfactant could lead to the decrement of 23-26%. The particle removal efficiencies were only 15-18% in the presence of polymer flocculate and slightly above that of water. The larger droplet of spray favored the agglomeration of inhalable particles. Increasing the surfactant concentration resulted in the higher removal of inhalable particle.


1994 ◽  
Vol 48 (11) ◽  
pp. 1428-1431 ◽  
Author(s):  
Yun-Bao Jiang ◽  
Xiu-Juan Wang

The fluorescence emission of p-dimethylaminochalcone (DMAC) has been monitored in β-cyclodextrin (β-CD) and cetyltrimethylammonium bromide (CTMAB) or sodium dodecylsulfate (SDS) mixture. In the presence of a fixed amount of β-CD, a peak-shaped variation is observed in the curve of DMAC fluorescence intensity vs. surfactant concentration below critical micelle concentration (cmc). The peak height is dependent on β-CD concentration, and no peak is noted in the absence of β-CD. Such a peak-shaped variation in DMAC fluorescence emission is shown to be direct evidence for β-CD-induced aggregation of the surfactant below cmc in aqueous solution. The 1:1 surfactant/β-CD inclusion complex is the hydrophobic source inducing the aggregation.


2015 ◽  
Vol 232 ◽  
pp. 93-110 ◽  
Author(s):  
Reshma A. Nandotaria ◽  
Chetna C. Chauhan ◽  
Rajshree B. Jotania

Strontium copper hexaferrite powder with composition Sr2Cu2Fe12O22 was synthesized in presence of a non-ionic surfactant Tween-80 using chemical co-precipitation route. The prepared samples were calcinated at 950 oC for 4 hrs in a furnace and then slowly cooled to room temperature to obtain Sr2Cu2Fe12O22 hexaferrite powder. The effect of surfactant concentration on phase formation, microstructure, magnetic and dielectric properties of Sr2Cu2Fe12O22 were investigated using XRD, SEM, TEM, VSM, dielectric and low field AC susceptibility measurement techniques. The XRD analysis reveals the formation of mixed phases of Y and M type hexaferrites. The synthesized samples exhibited magnetic properties typical for soft magnetic materials, with saturation magnetization typical for Y-type hexaferrites. The dielectric properties were studied within the frequency range 100 HZ to 2 MHz. SEM images show formation of non-uniform, spongy and porous structure. The low field AC susceptibility measurements indicate that formed Sr-Cu hexaferrite powder possesses ferrimagnetic to paramagnetic transition at Curie temperature.


1994 ◽  
Vol 303 (3) ◽  
pp. 907-914 ◽  
Author(s):  
A De la Maza ◽  
J L Parra

The structural transition stages induced by the interaction of the non-ionic surfactant Triton X-100 on phosphatidylcholine unilamellar vesicles were studied by means of static and dynamic light-scattering, transmission-electron-microscopy (t.e.m.) and permeability changes. A linear correlation was observed between the effective surfactant/lipid molar ratios (Re) (‘three-stage’ model proposed for the vesicle solubilization) and the surfactant concentration throughout the process. However, this correlation was not noted for the partition coefficients of the surfactant between the bilayer and the aqueous medium (K). Thus a sharp initial K increase was observed until a maximum value was achieved for permeability alterations of 50% (initial step of bilayer saturation). Further surfactant additions resulted in a fall in the K values until 100% of bilayer permeability. Additional amounts of surfactant led to an increase in K until bilayer solubilization. Hence, a preferential incorporation of surfactant molecules into liposomes governs the initial interaction steps, leading to the initial stage of bilayer saturation with a free surfactant concentration that was lower than its critical micelle concentration (c.m.c.). Additional amounts of surfactant increased the free surfactant until the c.m.c. was reached, after which solubilization started to occur. Thus the initial step of bilayer saturation was achieved for a smaller surfactant concentration than that for the Resat, although this concentration was the minimum needed for solubilization to start. Large unilamellar vesicles began to form as the surfactant exceeded 15 mol% (50% bilayer permeability), the maximum vesicle growth being attained for 22 mol% (400 nm). Thereafter, static light-scattering started to decrease gradually, this fall being more pronounced after 40 mol%. The t.e.m. picture for 40 mol% (Resat.) showed unilamellar vesicles, although with traces of smaller structures. From 50 mol% the size distribution curves began to show a bimodal distribution. The t.e.m. pictures for 50-64 mol% revealed tubular structures, together with open bilayer fragments. Thereafter, increasing amounts of surfactant (65-69 mol%) led to planar multilayered structures which gradually tended to form concentric and helicoidal conformations. The scattered intensity decreased to a low constant value at more than 71-72 mol%. However, the surfactant concentration for the Re(sol) (72.6 mol %) still presented traces of aggregated structures, albeit with mono-modal size-distribution curves (particle size of 50 nm). This vesicle size corresponded to the liposome solubilization via mixed-micelle formation.


Author(s):  
Felicia Alice Bayi ◽  
Amira Satirawaty Mohamed Pauzan

In emerging countries, heavy metal contamination is becoming more of a problem. Because of poor water and wastewater treatment, as well as increased industrial activities, heavy metal contamination in rivers, lakes, and other water sources has increased in developing countries. Non-ionic surfactants like Triton X-100 and Triton X-114 have been widely utilized to remove heavy metals from water, soil, and sediments via cloud point extraction and soil washing. The effectiveness of non-ionic surfactant to remove heavy metal was determined by the study of effect of the parameters which are pH, surfactant concentration, temperature, and presence of natural organic matter (NOM). Based on the overall study, non-ionic surfactant efficiency in removing heavy metals is strongly reliant on water and soil quality parameters such as pH, surfactant concentration, and temperature, as well as the surfactant's characteristics.


Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1831 ◽  
Author(s):  
Samhitha Kancharla ◽  
Nathan A. Zoyhofski ◽  
Lucas Bufalini ◽  
Boris F. Chatelais ◽  
Paschalis Alexandridis

The interaction in aqueous solutions of surfactants with amphiphilic polymers can be more complex than the surfactant interactions with homopolymers. Interactions between the common ionic surfactant sodium dodecyl sulfate (SDS) and nonionic amphiphilic polymers of the poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO-PPO-PEO) type have been probed utilizing a variety of experimental techniques. The polymer amphiphiles studied here are Pluronic F127 (EO100PO65EO100) and Pluronic P123 (EO19PO69EO19), having the same length PPO block but different length PEO blocks and, accordingly, very different critical micellization concentrations (CMC). With increasing surfactant concentration in aqueous solutions of fixed polymer content, SDS interacts with unassociated PEO-PPO-PEO molecules to first form SDS-rich SDS/Pluronic assemblies and then free SDS micelles. SDS interacts with micellized PEO-PPO-PEO to form Pluronic-rich SDS/Pluronic assemblies, which upon further increase in surfactant concentration, break down and transition into SDS-rich SDS/Pluronic assemblies, followed by free SDS micelle formation. The SDS-rich SDS/Pluronic assemblies exhibit polyelectrolyte characteristics. The interactions and mode of association between nonionic macromolecular amphiphiles and short-chain ionic amphiphiles are affected by the polymer hydrophobicity and its concentration in the aqueous solution. For example, SDS binds to Pluronic F127 micelles at much lower concentrations (~0.01 mM) when compared to Pluronic P123 micelles (~1 mM). The critical association concentration (CAC) values of SDS in aqueous PEO-PPO-PEO solutions are much lower than CAC in aqueous PEO homopolymer solutions.


Sign in / Sign up

Export Citation Format

Share Document