Surfactants-based remediation as an effective approach for removal of environmental pollutants—A review

Deterioration of environmental quality and equilibrium by rampant industrial expansion, accelerated urbanization and unchecked population growth has become a high-priority concern. The release of an alarming number of toxic polluting agents such as volatile organic compounds, dyes, heavy metals, pharmaceuticals, pesticides, industrial wastes, and personal care products due to natural or anthropogenic activities pose direct adverse effects on human health and living entities. This issue is inescapably increased because of the lack of efficient technologies for the proper disposal, management, and recycling of waste. It is of paramount importance to track alternative solutions to address these pollution problems for an eco-sustainable environment. Conventional remediation techniques are either inefficient, cumbersome or restricted due to certain techno-economic limitations. Environmental compatibility and high pollutant-removal efficacy make surfactants valuable for removal of organic pollutants and toxic heavy metal ions from different mediums. In this review, we present recent and up-to-date information on micelles/surfactants-assisted abatement of a vast number of toxic agents of emerging concern from water/wastewater including volatile organic compounds, personal care products, pharmaceutically active residues, toxic metals, dye pollutants, pesticides, and petroleum hydrocarbons. Based on the literature survey, it can be concluded that micelles-assisted water and soil treatment technology can have a better future on large-scale decontamination of wastewater. Though bio-surfactants are environmentally friendlier matrices and have successfully been employed for environmental decontamination; their large-scale applicability is challenging owing to high costs. Additional research efforts on the development and employment of novel bio-surfactants might render wastewater treatment technology greener, smarter and economical

Cleavable Surfactants: A Comparison between Ester, Amide, and Carbonate as the Weak Bond

Cleavable surfactants, i.e., surfactants in which a weak bond has deliberately been inserted into the molecule, are of interest when remaining surface-active material at a surface can cause problems. Ester and amide bonds are established as week linkages in surfactants but these generate an acid when they hydrolyze. For some applications, acidic degradation products are unwanted. Surfactants with a carbonate bond between the polar headgroup and the hydrophobic tail are of interest for such purposes. In this article, we compare the physical–chemical properties of nonionic carbonate surfactants with those of the corresponding ester and amide surfactants. The half-lives of the different cleavable surfactants are also compared and it was found that a carbonate bond is slightly more stable to alkaline hydrolysis than an ester bond when present in otherwise identical structures. A nonionic Gemini surfactant with a carbonate bond in the spacer, which on hydrolysis decomposes into two identical single-tailed nonionic amphiphiles, is also presented. The hydrolysis kinetics for this surfactant was studied in some detail and it was found that it degrades much faster at low temperature than at higher temperature. This anti-Arrhenius type of hydrolysis kinetics is proposed to be due to the reverse solubility versus temperature behavior of ethoxylated surfactants

A review on microplastic emission from textile materials and its reduction techniques

Publisher Copyright: © 2022The production and consumption of textiles is continuously increasing due to the growth of population and fast fashion. Fiber fragments (1 µm–5 mm) released from garments and home textiles during washing, drying, and wearing are considered a new source of environmental pollution and health hazard. Fiber fragments can be ingested by aquatic animals and substantially threaten their metabolic activities. Small fiber fragments can also enter our food chain by the consumption of sea creatures, sea table salt, and drinking water. In this paper, we overview various important parameters on the release of fiber fragments from garments, and home textiles including the type of fabric, weaving/knitting structure, detergent type and concentration, temperature, pH, spin-speed, and duration of the washing and drying processes. The influence of various mechanical and chemical textile finishes on the release of fiber fragments is explained. Any process that reduces the strength of fibers and their interactions including sanding, brushing, bleaching can potentially increase the release of fiber fragments in consecutive wet processes. We highlight some of the most important environmental regulations on the release of microplastics and fiber fragments to the environment and provide a series of recommendations to reduce the impact.Peer reviewe

Advances in Preparation Methods and Conductivity Properties of Graphene-based Polymer Composites

Publisher Copyright: © 2023, The Author(s).Graphene-based polymer composites with improved physical properties are of great interest due to their lightweight, conductivity, and durability. They have the potential to partially replace metals and ceramics in several applications which can reduce energy and cost. The obtained properties of graphene-based polymer composites are often linked to the way graphene is dispersed in the polymer matrix. Preparation techniques like solution mixing, melt blending, and in-situ polymerization have been used to obtain graphene-based polymer composites. Dispersing and aligning graphene fillers within the composite is a key factor in enhancing the thermal and electrical conductivity values of the composites due to graphene’s anisotropic properties. The effect of the preparation methods of these composites on their physical-chemical properties is discussed in this review where we presented the advances that were achieved so far in the preparation techniques used showing the highest values ever achieved for electrical andthermal conductivity for these graphene-based polymer composites. Also, we presented the possible applications where graphene-based composites can be utilized.Peer reviewe

Cationic ester-containing gemini surfactants: Adsorption at tailor-made surfaces monitored by SPR and QCM

Adsorption of a series of ester-containing cationic surfactants at a surface containing 90% methyl groups and 10% carboxyl groups was studied by two surface analysis techniques, surface plasmon resonance (SPR) and quartz crystal microbalance (QCM). Such a surface, which is at the same time hydrophobic and negatively charged, is of interest as a model for many polymeric surfaces. Two different types of ester gemini surfactants and their monomeric counterparts were included together with nonester containing surfactants of similar structure. The results show that the gemini surfactants give the same adsorbed amount at the surface as the monomeric surfactants when compared at the same bulk concentration normalized to the critical micelle concentration (cmc) in bulk. Since the cmc of the geminis is around 20 times lower than the cmc of the corresponding monomeric surfactants, the gemini surfactants are much more effective in covering the surface. The two techniques gave similar relative values but the QCM values were always higher than those from SPR, which is due to the former method taking also adsorbed water into account. The adsorption, as measured by both methods, was found to follow closely the Langmuir adsorption model

Cationic Ester-Containing Gemini Surfactants: Physical-Chemical Properties

Three ester-containing cationic gemini surfactants, two with decanoyl chains and either a three-carbon or a six-carbon spacer unit and one with dodecanoyl chains and a three-carbon spacer, were synthesized and evaluated. A corresponding monomeric cationic ester surfactant was used for comparison. This type of amphiphile, a so-called esterquat, is known to undergo rapid hydrolysis above the critical micelle concentration because of micellar catalysis. The esterquat geminis of this work were found to be much more susceptible to hydrolysis than the esterquat monomer. This difference is believed to be caused by anchimeric assistance by the second cationic headgroup in the gemini amphiphiles. However, there is no correlation between the rate of chemical hydrolysis and the rate of biodegradation. The monomeric esterquat, which is the most stable in the chemical hydrolysis experiments, was the only surfactant that passed the test for “readily biodegradable”. We also observed a considerable difference in the hydrolysis rate within the small series of gemini surfactants. The amphiphile with two decanoyl chains and a three-carbon spacer, N,N′-bis(2-(decanoyloxy)ethyl)-N,N,N′,N′-tetramethyl-1,3-propanediammonium dibromide, had the fastest rate of hydrolysis. This surfactant also exhibited a considerably lower degree of micelle ionization than the other surfactants, which is believed to be due to the closer proximity of the charged groups on the micelle surface. A small distance between headgroups will give more pronounced neighboring group participation, accounting for the increased rate of hydrolysis. An interesting property of the surfactant that is the most susceptible to hydrolysis is that it gives rise to an extremly stable foam. We propose that the foam stability is a result of the partial hydrolysis of the surfactant generating sodium decanoate, an anionic surfactant, that forms a mixed film with the starting cationic gemini surfactant. It is known that mixed monolayers in which there is a strong attractive interaction between surfactant headgroups can lead to stable foams