Antimicrobial polyethylene terephthalate (PET) treated with an aromatic N‐halamine precursor,m‐aramid

A commercial m‐aramid as N‐halamine precursor has been coated onto polyethylene terephthalate (PET) fabric surface by pad‐dry‐curing process. The process is accomplished by padding the scoured PET fabric through the homogeneous m‐aramid solution, drying at 150°C for 3 min, and curing at 230°C for 3 min. The PET surface coated with m‐aramid was characterized using fourier transform infrared‐attenuated total reflection (FTIR‐ATR) spectroscopy, X‐ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM). FTIR exhibits new bands in the 1645 and 1524 cm^?1 regions as characteristic of m‐aramid bands, which indicate the PET fabric coated with m‐aramid. XPS results show a distinguishable peak at binding energy 398.7 eV, which confirms the nitrogen atom of m‐aramid on the PET surface. In addition, SEM image shows a layer of coating onto the PET surfaces, which demonstrates the presence of m‐aramid coating on the surface of the PET. After exposure to dilute sodium hypochlorite solution, exhibition of antimicrobial activity on the coated PET is attributed to the conversion of N‐halamine moieties from the N‐halamine precursor. The chlorinated PET showed high antimicrobial activity against Gram‐negative and Gram‐positive bacteria. The chlorinated PET coated with 10% m‐aramid exhibited about 6 log reductions of S. aureus and E. coli O157:H7 at a contact time of 10 and 30 min, respectively. Furthermore, the antimicrobial activity was durable and rechargeable after 25 wash cycles. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of N,N‐diethyl‐m‐toluamide on the structure and dyeing properties of meta‐aramid and para‐aramid fibre

N,N‐Diethyl‐m‐toluamide has been widely used in the mosquito‐repellent finishing of textiles over the past few decades, but the use of N,N‐diethyl‐m‐toluamide as a dye carrier for aramid dyeing with disperse dye has been seldom reported. Meanwhile, the application of aramid fibre in clothing is limited because it is difficult to dye. In this work, the effect of N,N‐diethyl‐m‐toluamide on the dyeing properties of aramid fibre was examined by measuring the percentage disperse dye exhaustion under different conditions. In order to understand the mechanism by which N,N‐diethyl‐m‐toluamide promotes the exhaustion of disperse dye on aramid fibre, the ultraviolet‐visible spectrum of the dye and N,N‐diethyl‐m‐toluamide solution, the glass transition temperature, the crystalline structure, and the degree of orientation of aramid fibre treated with N,N‐diethyl‐m‐toluamide were measured by ultraviolet‐visible spectrophotometry, differential scanning calorimetry, X‐ray diffraction analysis, and velocity‐oriented tests respectively. The results indicated that N,N‐diethyl‐m‐toluamide not only could reduce the glass transition temperature and degree of orientation of aramid fibre but could also improve the solubility of disperse dye in aqueous solution, and therefore could enhance the percentage disperse dye uptake on aramid fibre, whereas treatment with N,N‐diethyl‐m‐toluamide showed little effect on the crystalline structure of aramid fibre. The results implied that N,N‐diethyl‐m‐toluamide was beneficial to the diffusion of disperse dye molecules into the amorphous region of aramid fibre under the dyeing conditions, but seldom affected the mechanical properties of aramid fibre.     

Breathable properties of m‐Aramid nanofibrous membrane with high thermal resistance

Electrospinning of m‐aramid in dimethyl acetamide/LiCl solution was investigated to develop thermo‐resistant nanofibrous membranes for breathable waterproof materials. The m‐aramid nanofibers were continuously generated and densely mounted to the membrane without the blockage of the spinning tip during electrospinning. In order to obtain the electrospun m‐aramid nanofibers with different fiber diameters, the polymer concentration in the solution and the spinning distance were varied. Electrospun m‐aramid nanofibrous membranes of various fiber diameters and thicknesses were prepared, and then compared with two commercial expanded polytetrafluoroethylene (ePTFE) membranes with respect to water vapor permeability and pore size. The m‐aramid nanofibrous membrane showed a good water vapor permeability that satisfied the criterion of a breathable membrane, higher than those of the ePTFE porous membranes. Therefore, m‐aramid nanofibrous membrane with thermal and mechanical resistance has great potential for breathable waterproof materials and filters. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41515.     

Sand/charcoal N‐halamine blends for water treatment

N‐halamine polymeric material based on cellulose extracted from an agricultural waste (rice straw) was blended with sand/charcoal for disinfection purposes. The presence of N‐halamine between sand/charcoal particles in water filters prevents internal bacterial growth and kills filtered cells especially in the deep and lower parts of the filters. N‐halamine was blended with sand/charcoal with different ratios, 1:3, 1:2, 1:1, 2:1, and 3:1, and their antimicrobial activity was evaluated using different methods such as agar plate, agar blend, stirred flask, and column methods. Increasing the ratio of the cellulosic N‐halamine provides further filtration and disinfection action in water in addition to securing a clean medium between sand/charcoal particles especially in columns as models for water filters. The ratio 1:1 (sand/charcoal: N‐halamine) was found to be suitable for producing a recyclable water filter and recyclable water purification unit based on sand/charcoal‐ N‐halamine blends. POLYM. COMPOS., 35:2137–2143, 2014. © 2014 Society of Plastics Engineers     

Tailoring of water‐soluble cellulose‐g‐ copolymers in homogeneous medium using single‐electron‐transfer living radical polymerization

Cellulose‐graft‐polyacrylamide and cellulose‐graft‐poly(N,N‐dimethylacrylamide) copolymers were prepared by single‐electron‐transfer living radical polymerization (SET‐LRP) in homogeneous medium. Cellulose macroinitiators for SET‐LRP, with different numbers of initiating sites along the cellulose backbone, were successfully synthesized by direct acylation of cellulose with 2‐bromoisobutyryl bromide in LiCl/dimethylacetamide. Dynamic light scattering revealed that cellulose macroinitiator molecules in dimethylsulfoxide (DMSO) exist primarily as individual chains with a certain amount of intermolecular aggregates. SET‐LRP of acrylamide and N,N‐dimethylacrylamide with the cellulose macroinitiators was carried out in DMSO solution. Formation of cellulose‐graft‐copolymers was confirmed using attenuated total reflectance Fourier transform infrared, ¹H NMR and ¹³C NMR spectroscopy, and the products were water‐soluble. High content of poly(N,N‐dimethylacrylamide) in the copolymers enhanced the thermal stability relative to that of cellulose. Scanning electron microscopy studies of cellulose‐based particles formed from the copolymers using the aerosol flow reactor method revealed spherical nanoscale structures. Copyright © 2011 Society of Chemical Industry     

Antimicrobial polyester

Two N‐halamine siloxane precursors, 5,5‐dimethyl‐3‐(3′‐triethoxysilylpropyl)hydantoin and 3‐(3′‐triethoxysilylpropyl)‐7,7,9,9‐tetramethyl‐1,3,8‐triazaspiro[4.5]decane‐2,4‐dione, have been synthesized and coated onto polyester fiber surfaces. The coated polyester was rendered biocidal after exposure to household bleach solution by converting the heterocyclic precursors to N‐halamine moieties. The thermal properties of these coated polyester samples were determined with differential scanning calorimetry. The chlorinated polyester swatches were challenged with Staphylococcus aureus (ATCC 6538) and Escherichia coli O157 : H7 (ATCC 43895) with contact times ranging from 1 to 30 min. The biocidal testing showed that the chlorinated samples inactivated S. aureus and E. coli O157 : H7 within 5 and 30 min of contact, respectively. Standard washing tests indicated that the chlorinated coated fibers were very resistant to loss of the coating through hydrolyses. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Corrosion behaviour of some stainless steels in chlorinated Gulf seawater

The corrosion resistance of conventional and high alloy stainless steels (specifically 316L, 317L, 904L, duplex 2205, 3127hMO, 1925hMO, 254SMO, 654SMO and Remanit-4565) was determined electrochemically in chlorinated and unchlorinated Arabian Gulf Seawater at 25 and 50 °C. The stainless steels 316L and 317L were used as reference alloys. The electrochemical potentiodynamic cyclic polarization method was used to determine the passive film break down potential (E _b), protection potential (E _prot) and maximum current attained on scan reversal (I _max). It was found that at 25 °C in chlorinated and unchlorinated seawater and at 50 °C in unchlorinated seawater, stainless steels 316L and 317L have poor resistance to corrosion, Stainless steels 904L and duplex 2205 at 25 °C in chlorinated and unchlorinated seawater showed good resistance to corrosion but at 50 °C these steels failed to resist. The high alloy stainless steels such as 3127hMO, 1925hMO, 254SMO, 654SMO and Remanit-4565 showed better corrosion resistance under all the test conditions.     

Optical resolution of (R,S)‐2‐phenyl‐1‐propanol through enantioselective ethycellulose membranes

Enantioselective membrane was prepared using ethyl cellulose (EC) as membrane material. The flux and permselective properties of membrane using aqueous solution of (R,S)‐2‐phenyl‐1‐propanol as feed solution was studied. The employed membrane process was a pressure driven process. All kinds of important conditions including preparation and operation of membranes were investigated in this experimentation. When the membrane was prepared with 18 wt % EC, 20 wt % N,N‐dimethylformamide in casting solution, 13 min evaporation time and 0°C temperature of water bath for the gelation of the membrane, and the operating pressure and feed solution of (R,S)‐2‐phenyl‐1‐propanol were 0.2 MPa and 1.5 mg/mL, respectively, over 90% of enantiomeric excess (e.e.) and 44.2 (mg/m² h) of flux were obtained. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

New aramid‐based nanocomposites: Synthesis and characterization

New type of nanocomposites containing various proportions of montmorillonite in aromatic polyamide was prepared via solution intercalation method. Aramid chains were synthesized by reacting 4,4′‐oxydianiline with isophthaloyl chloride in N,N′‐dimethyl acetamide. Dodecylamine was used as swelling agent to change the hydrophilic nature of montmorillonite into organophilic. Appropriate amounts of organoclay were mixed in the polymer solution using high‐speed mixer for complete dispersion of the clay. Thin films cast from these materials after evaporating the solvent were characterized by XRD, TEM, mechanical, thermal, and water absorption measurements. The structure and morphology of the nanocomposites determined by XRD and TEM revealed the formation of exfoliated and intercalated clay platelets in the aramid matrix. Mechanical data indicated improvement in the tensile strength and modulus of the nanocomposites with clay loading up to 6 wt%. The glass transition temperature increased up to 12 wt% clay content and thermal stability amplified with increasing clay loading. The water absorption reduced gradually as a function of organoclay and approached to zero with 20 wt% organoclay in the aramid. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Synthesis and Properties of N‐Alkyl–N,N‐Dimethyl‐N‐(o‐Hydroxymethyl)Benzylammonium Chlorides

A series of N‐alkyl–N,N‐dimethyl‐N‐(o‐hydroxymethyl)benzylammonium chlorides surfactants (DHBA‐m) were synthesized using o‐chloromethylbenzyl alcohol and N‐alkyl–N,N‐dimethyl tertiary amine as raw materials. The structure of the products was confirmed by FT‐IR, ¹H NMR, ¹³C NMR and MS. DHBA‐m surfactants exhibit low Krafft points and high surface activities. The process of micellization of DHBA‐m is spontaneous, exothermic, and entropy‐driven. The hydroxymethyl substitution increases hydrophobicity of DHBA‐m, thus making micellization more favorable compared with that of N‐dodecyl–N,N‐dimethyl‐N‐benzylammonium chlorides (DDBAC‐m). The bactericidal activity of DHBA‐m is stronger on E. coli than that of DDBAC‐12, and DHBA‐16 shows strong bactericidal activity on Salmonella, S. aureus, and Streptococcus.     

Effect of Li+ ions on structure,properties, and actuation of cellulose electro‐active paper actuator

We have reported an electro‐active paper actuator from regenerated cellulose. After dissolving cellulose fibers with a solution of lithium chloride in N,N‐dimethylacetamide, cellulose was regenerated by combining distillation of cellulose solution along with washing with the mixture of deionized water, isopropyl alcohol, and running water. However, the effect of Li⁺ ions on structure, properties, and the actuation behavior of the actuator was not studied. This article describes the changes in these parameters when the Li⁺ ions are removed by subjecting it to different running water exposure time. The structure and properties of cellulose electro‐active paper and its actuation behavior were studied. As Li⁺ ions content reduced from 4354.17 to 10.26 ppm by increasing the exposure time of running water, crystallinity, Young's modulus, and bending displacement decreased. Details about the investigation have been explained. This elimination of ions is important to increase the piezoelectric effect in EAPap by decreasing the ion migration effect. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Preparation and properties of chemical cellulose from ascidian tunic and their regenerated cellulose fibers

Chemical cellulose (dissolving pulp) was prepared from ascidian tunic by modified paper‐pulp process (prehydrolysis with acidic aqueous solution of H₂SO₄, digestion with alkali aqueous solution of NaOH/Na₂S, bleaching with aqueous NaOCl solution, and washing with acetone/water). The α‐ cellulose content and the degree of polymerization (DPw) of the chemical cellulose was about 98 wt % and 918, respectively. The Japanese Industrial Standard (JIS) whiteness of the chemical cellulose was about 98%. From the X‐ray diffraction patterns and ¹³C‐NMR spectrum, it was found that the chemical cellulose obtained here has cellulose Iβ crystal structure. A new regenerated cellulose fiber was prepared from the chemical cellulose by dry–wet spinning using N‐methylmorpholine‐ N‐oxide (NMMO)/water (87/13 wt %) as solvent. The new regenerated cellulose fiber prepared in this study has a higher ratio of wet‐to‐dry strength (<0.97) than commercially regenerated cellulose fibers. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1634–1643, 2002.     

New chlorine‐resistant polyamide reverse osmosis membrane with hollow fiber configuration

New asymmetric hollow fiber reverse osmosis (RO) membrane was developed from a new chlorine‐resistant copolyamide [4T‐PIP(30)] with a piperazine moiety by a conventional phase‐separation method. The new 4T‐PIP(30) hollow fiber membrane has the same low‐pressure RO performance as cellulose triacetate hollow fiber membrane (FR = 205 L/m² day, Rj = 99.6%) and superior chlorine resistance as well as pH resistance to conventional aramid RO membranes. Structural analysis and viscoelastic study revealed that the new hollow fiber consisted of a top skin, dense layer, and microporous layer, and that it began to decrease its elasticity at 80°C in water, which is possibly related to its good and stable RO performance around room temperature. Several kinds of RO modules were made from the new hollow fiber membranes, for which RO performances were stable for 2 years in chlorinated feed water desalination (the free residual chlorine ranged from 0.l to 1.1 mg/L). © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 517–527, 2001     

Surface‐active amphiphilic poly[(2‐acrylamido‐2‐methylpropanesulfonic acid)‐co‐(N‐isopropylacrylamide)] nanoparticles as stabilizer in aqueous emulsion polymerization

This work reports the effect of nanogel solid particles on the surface and interfacial tension of water/air and water/styrene interfaces. Moreover, the work aimed to use nanogels as a stabilizer for miniemulsion aqueous polymerization. A series of amphiphilic crosslinked N‐isopropylacrylamide (NIPAm) and 2‐acrylamido‐2‐methylpropanesulfonic acid (AMPS) copolymer nanogels were synthesized based on an aqueous copolymerization batch method. Divinylbenzene and N,N‐methylene bisacrylamide were used as crosslinkers. The morphologies of the prepared nanogels were investigated using transmission and scanning electron microscopies. The lower critical transition temperatures were determined using differential scanning calorimetry. The surface tension of colloidal NIPAm/AMPS dispersions was measured as functions of surface age, temperature and the morphology of the NIPAm/AMPS nanogels. The NIPAm/AMPS nanogels reduced the surface tension of water to about 30.1 mN m^?1 at 298 K with a small increase at 313 K. Surface activities of these nanogels in water were determined by surface tension measurements. The NIPAm/AMPS dispersions had high surface activity and were used as a stabilizer to prepare a crosslinked poly(styrene‐co‐AMPS) microgel based on emulsion crosslinking polymerization. © 2013 Society of Chemical Industry     

Nanocomposite films of poly(vinylidene fluoride) filled with polyvinylpyrrolidone‐coated multiwalled carbon nanotubes: Enhancement of β‐polymorph formation and tensile properties

To improve interactions between carbon nanotubes (CNTs) and poly(vinylidene fluoride) (PVDF) matrix, multiwalled CNTs (MWCNTs) were successfully coated with amphiphilic polyvinylpyrrolidone (PVP) using an ultrasonication treatment performed in aqueous solution. It was found that PVP chains could be attached noncovalently onto the nanotubes' surface, enabling a stable dispersion of MWCNTs in both water and N,N‐dimethylformamide. PVP‐coated MWCNTs/PVDF nanocomposite films were prepared by a solution casting method. The strong specific dipolar interaction between the PVP's carbonyl group (C?O) and the PVDF's fluorine group C?F₂ results in high compatibility between PVP and PVDF, helping PVP‐coated MWCNTs to be homogenously dispersed within PVDF. Fourier transform infrared and X‐ray diffraction characterization revealed that the as‐prepared nanocomposite PVDF films exhibit a purely β‐polymorph even at a very low content of PVP‐wrapped MWCNTs (0.1 wt%) while this phase is totally absent in the corresponding unmodified MWCNTs/PVDF nanocomposites. A possible mechanism of β‐phase formation in PVP‐coated MWCNTs/PVDF nanocomposites has been discussed. Furthermore, the tensile properties of PVDF nanocomposites as function of the content in PVP‐coated MWCNTs were also studied. Results shows that the addition of 2.0 wt% of PVP‐coated MWCNTs lead to a 168% increase in Young's modulus and a 120% in tensile strength. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Cellulose/acrylic acid copolymer blends for films and coating applications

Enzymatically treated cellulose was dissolved in a NaOH/ZnO solvent system and mixed together with poly(ethylene‐co‐acrylic acid) (PE‐co‐AA) or poly(acrylamide‐co‐acrylic acid) (PAA‐co‐AA) polymers, in order to improve the properties of dissolved cellulose and to prepare homogeneous cellulose‐based blends for films and coatings. The solution stage properties of the blends were evaluated by rheological methods and the precipitated dry blends were characterized by dynamic mechanical analysis, differential scanning calorimetry, and scanning electron microscopy. Paperboard coating tests done at laboratory scale showed dissolved cellulose/acrylic acid copolymer‐based blends function well as coating materials. All of the tested blends showed a good resistance against grease in the coating trials, having grease resistance from 60 to 69 days despite a very thin (～2 µm) coating layer. In addition, cellulose/PE‐co‐AA coating showed improved water vapor and oxygen barrier properties when compared with neat dissolved cellulose‐coated paperboard. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40286.     

Grafting of poly[styrene‐co‐N‐(4‐vinylbenzyl)‐N,N‐diethylamine] polymer film onto the surface of silica microspheres and their application as an effective sorbent for lead ions

Amino containing polymer of poly[styrene‐co‐N‐(4‐vinylbenzyl)‐N,N‐diethylamine] (PS‐co‐PVEA) was successfully grafted onto the surface of silica microspheres via the seed dispersion polymerization of styrene and N‐(4‐vinylbenzyl)‐N,N‐diethylamine in the presence of divinylbenzene employing the 3‐(methacryloxy)propyltrimethoxysilane activated silica microspheres as the seed. The polymerization led to thin chelating polymer films (30 nm) coated silica microspheres (silica@polymer) as determined by transmission electron microscopy. The synthesized silica@polymer composites were used as sorbents for lead ions (Pb²⁺). The adsorption properties, such as the pH effect, the adsorption kinetic, adsorption isotherm as well as the reuse of the silica@polymer sorbent were evaluated. The results demonstrated that the optimized adsorption condition was under neutral and the silica@polymer sorbent was efficient since it showed higher adsorption amounts (8.0 mg/g) and shorter adsorption equilibrium time (8 h) than that of the PS‐co‐PVEA microspheres and the pristine silica microspheres. Moreover, the silica@polymer sorbent was reusable even after four cycles of adsorption. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 39973.     

Ceria‐coated diesel particulate filters for continuous regeneration

The potential of diesel particulate filters wash‐coated with highly dispersed nano‐metric ceria particles for continuous regeneration has been investigated. To this end, catalytic filters were prepared, soot‐loaded (avoiding the formation of the cake layer), and regenerated—under isothermal conditions—at temperature ranging from 200–600°C. Results have shown that catalytic oxidation of soot starts from 300°C and, at all temperatures, the selectivity to CO₂ is higher than 99%. 475°C is the minimum temperature at which the filter is regenerated via catalytic path. At this temperature, the catalytic filter maintains substantially the same performance over repeated cycles of soot loading and regeneration, indicating that the thermal stability of ceria is preserved. This has been further confirmed by comparison between the outcomes obtained from characterization (X‐ray powder diffraction, N₂ adsorption at 77 K, Hg intrusion porosimetry, and scanning electron microscope/energy dispersive X‐ray analysis) of fresh filter and filter subjected to repeated regeneration tests. © 2017 American Institute of Chemical Engineers AIChE J, 63: 3442–3449, 2017     

Electrolyte and pH responsive surfactant association in ionic semi‐interpenetrating networks containing cellulose or chitin synthesized in lithium chloride–N,N‐dimethylacetamide

Semi‐interpenetrating networks (SIPNs) of N,N‐dimethylacrylamide (DMAm)–N,N‐dimethylamino‐ethylacrylamide (DMAEAm), or N,N‐dimethylacrylamide (DMAm)–2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid (AMPS) containing cellulose or chitin were synthesized in 9% LiCl–N,N‐dimethylacetamide (DMAc). The SIPNs were formulated to contain (1, 2, or 5% w/w) cellulose or 0.8% w/w chitin. Control systems (without polysaccharide) were also synthesized in 9% LiCl–DMAc. An acrylamide (Am)–AMPS hydrogel was synthesized for comparison with the SIPN composites. The swelling behavior of these materials was investigated as a function of pH (DMAEAm‐containing networks) or electrolyte concentration (AMPS‐containing networks). The DMAm–AMPS materials were found to have higher equilibrium water content (EWC) values in deionized water than the DMAm–DMAEAm materials. The EWC of the DMAm–DMAEAm materials was largest between pH 4 and 5 due to the protonation of the tertiary amine, with the chitin‐containing material exhibiting the largest EWC. The DMAm–AMPS materials exhibited a decrease in EWC values with an increase in electrolyte concentration. Polymer–surfactant interactions were shown to exist for surfactants of opposite charge of the ionic mer units incorporated into the polymeric network. Surfactant sequestration by the polysaccharide‐containing materials was greater than that of the control gels; however, the rates of surfactant binding were lower. Release of the bound surfactant was achieved by the disruption of the charge–charge interactions by changing the pH of the medium (DMAEAm‐containing networks) or by the addition of electrolyte (AMPS‐containing networks). The DMAm–DMAEAm SIPNs released only 4% of the surfactant originally sequestered. By contrast, the DMAm–AMPS SIPNs released approximately 80%. The control Am–AMPS hydrogel–surfactant complex collapsed in the presence of electrolyte, and no surfactant was released from the complex. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 989–998, 1999     

Synthesis,Characterization and Properties of <Emphasis Type="Italic">N</Emphasis>-Alkyl-<Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>-di(2-hydroxyethyl) Amine Oxides

N‐Dodecyl‐N,N‐di(2‐hydroxyethyl) amine oxide (C₁₂DHEAO) and N‐stearyl‐N,N‐di(2‐hydroxyethyl) amine oxide (C₁₈DHEAO) were synthesized with N‐alkyl‐diethanolamine and hydrogen peroxide. Their chemical structures were confirmed using ¹H‐NMR spectra, mass spectral fragmentation and FTIR spectroscopic analysis. It was found that C₁₂DHEAO and C₁₈DHEAO reduced the surface tension of water to a minimum value of approximately 28.75 mN m^?1 at concentration of 2.48 × 10^?3 mol L^?1 and 32.45 mN m^?1 at concentration of 5.21 × 10^?5 mol L^?1, respectively. The minimum interfacial tension (IFT_min) and the dynamic interfacial tension (DIT) of oil–water system were measured. When C₁₈DHEAO concentration was in the range of 0.1–0.5%, the IFT_min between liquid paraffin and C₁₈DHEAO solutions all reached the ultra‐low interfacial tension. Furthermore, their foam properties were investigated by Ross‐Miles method, and the height of foam of C₁₂DHEAO was 183 mm. It was also found that they showed strong emulsifying power.