Breaking waves aerate seawater surfaces and form whitecaps in the open ocean. The aerated surface area, or whitecap coverage, has been used to macroscopically parametrize air–sea momentum and gas exchange. However, the microscopic mechanisms of the generation, evolution and attenuation of surface bubbles in whitecaps remain poorly understood. In this study, we examined the size distributions and size-dependent lifetimes of surface bubbles generated by water sheet entry and air injection on a porous plate during the clustering, coalescing and bursting processes, depending on surfactant concentrations and bubble mobility. Mechanisms of coalescence through film thinning of adjacent bubble walls owing to the inter-bubble attraction and Marangoni forces experimentally described the surfactant-dependent bubble growth, finally achieving bubble bursting, which were statistically characterized in a population balance analysis. Lagrangian bubble lifetimes were described by the Weibull distribution, providing that surfactant in seawater extended the probabilistic survival periods of surface bubbles two times longer than those of clean bubbles.

Retinopathy of prematurity (ROP) is a leading cause of blindness in premature infants. The condition is associated with DHA deficiency. This study aimed to investigate the effect of DHA supplementation on the occurrence of ROP in infants receiving oral oil drops. It is part of the Joinville DHA study, a non-parallel-group cohort study conducted from March 2020 to January 2023 at a public maternity hospital in Brazil. Infants born before 33 weeks of gestational age or with a birth weight ≤ 1500 g were recruited. Among 155 infants, 81 did not receive and 74 received DHA supplementation until complete vascularisation of the peripheral retina. There was a higher incidence of infants with ROP in the unsupplemented group (58·6 %) compared with the DHA group (41·4 %), but this difference was NS (P = 0·22). Unadjusted logistic regression analysis showed that patent ductus arteriosus and neonatal corticosteroids were significantly (P < 0·05) associated with ROP in both groups. In the DHA group, surfactant use was also associated with ROP (P = 0·003). After adjusting for important covariates, patent ductus arteriosus and neonatal corticosteroids continued to be significant for infants in the unsupplemented group (OR = 3·99; P = 0·022 and OR = 5·64; P = 0·019, respectively). In the DHA group, only surfactant use continued to be associated with ROP (OR = 4·84; P = 0·015). In summary, DHA supplementation was not associated with ROP. Further studies are necessary to better understand the relationship between DHA supplementation, ROP and associated comorbidities.

Hydrophobicity, swellability, and dispersion are important properties for organo-montmorillonites (OMnt) and have yet to be fully characterized for all OMnt configurations. The purpose of the present work was to examine the preparation of OMnt from the reaction of Ca2+-montmorillonite (Ca2+-Mnt) with a high concentration of surfactant and to reveal the relevant properties of hydrophobicity and dispersion of the resultant OMnt. A series of OMnt samples were prepared using a small amount of water and cetyltrimethylammonium bromide (CTAB) with a concentration more than the CTAB critical micelle concentration (CMC). The relationship between OMnt microstructure and the hydrophobicity and swellability properties was investigated in detail. The resulting OMnt samples were characterized using powder X-ray diffraction patterns (XRD), Fourier-transform infrared (FTIR) spectroscopy, thermogravimetric and differential thermogravimetry (TG-DTG), water contact angle tests, swelling indices, and transmission electron microscopy (TEM). The addition of CTAB and water in the OMnt preparation affected the OMnt microstructure and properties. An increase in CTAB concentration led to a more ordered arrangement of cetyltrimethylammonium (CTA+) cations in the interlayer space of the OMnt and a large amount of CTA+ cations on the outer surfaces of the OMnt. The swelling indices and the water contact angles of OMnt samples depended on the distribution of the CTAB surfactant on OMnt and the orientation of the surfactant hydrophilic groups on the inner and on the outer surfaces of OMnt. A maximum swelling index of 39 mL/g in xylene was achieved with an average water contact angle of 62.0° ± 2.0° when the amount of CTAB added was 2 times the cation exchange capacity (CEC) of Mnt and the lowest water to dry Mnt mass ratio was 3 during the preparation of OMnt samples. The platelets of OMnt aggregated together in xylene by electrostatic attraction and by hydrophobic interactions.

Waterproofing treatment is important for the preservation of smectite-rich rocks because of their shrinking and swelling properties. The effects of water repellents on the smectite structure and the water sorption of untreated and treated smectites were studied using X-ray diffraction. The hydrophobic Wacker BS 290 (around 100% silane/siloxane) does not prevent water from sorbing on the interlayer surface of smectite because the hydrophobic silane/siloxane is not intercalated into the interlayer space, but adsorbed onto the external surface of smectite. However, the hydrophilic Wacker BS 1001 (water-soluble emulsified silane/siloxane) prevents water from sorbing onto the interlayer surface beyond 33.3 wt.% because the hydrophobic part of the intercalated surfactant has a poor affinity for water. These results imply that water repellent containing a surfactant is suitable for smectite-rich rocks, but the expansion of smectite by intercalation of the surfactant is likely to influence volume change in smectite-rich rocks. This study notes that smectite within a rock can be one of the most important factors influencing the effectiveness of waterproof treatment. This study proposes that an intensive preliminary examination should be performed before applying water repellents to rocks, and furthermore, encourages development of new chemical reagents suitable for protecting smectite-rich rocks from moisture.

The adsorption of hexadecyltrimethylammonium (HDTMA) in smectite was studied by adsorption isotherms, X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Smectites that had reacted for 48 h with HDTMA cations equivalent to 0.2–3.0 times the cation exchange capacity (CEC) were converted to HDTMA-exchanged smectites with various d-spacings. Study of HDTMA-smectites by HRTEM suggests that the HDTMA adsorption results in interlayer expansion with various d-spacings and irregular wavy layer structures. We believe that HDTMA loading beyond the CEC of smectite affects the structure of clay by the additional adsorption of HDTMA-Br− via hydrophobic bonding. Surfactant orientation probably depends on the quantity of surfactant in the interlayer. Our TEM study shows that the structure of the adsorbed HDTMA layer in the interlayers of smectite depends on the charge distribution and chemical composition of smectite.

The most potent and significant polyphenolic molecule from tea catechins is epigallocatechin gallate (EGCG); it has potential anti-cancer and anti-inflammatory properties. Methods are needed to mitigate its presence in the environment and protect humans from exposure. The objective of the present study was to investigate a functionalized, low-cost clay mineral as an adsorbent for the tea polyphenol EGCG. Hydrophilic bentonite (Bn) was functionalized using Aliquat 336 (A336) and isobutyl(trimethoxy)silane (IBTS). The degree of clay functionalization depended on the extent of introduction of alkyl linkages between the superimposed clay layers. Results revealed that Aliquat 336 functionalized clay (A336-Bn) exhibited maximum thermal stability at 500°C and it is a promising adsorbent for ECGC with a maximum adsorption capacity of 196.26 mg/g at equilibrium. Experimental data were analyzed using pseudo-first order and pseudo-second order models. Adsorption isotherms were interpreted from the Freundlich adsorption isotherm.

The transformation of clay minerals into organo-clays by surfactant intercalation is of great environmental and industrial importance because it causes the clay to attract hydrophobic contaminants and other non-polar organic compounds, but a better understanding is needed of the mechanisms by which different classes of surfactants are intercalated. The purpose of this study was to synthesize and characterize an organo-clay comprising triethylene glycol monodecyl ether (C10E3) non-ionic surfactant, which has a lamellar phase at room temperature, intercalated into Ca-montmorillonite from Wyoming (SWy-2). The C10E3 non-ionic surfactant differed from previous non-ionic surfactants used in the formation of a lamellar phase in that it consisted of the stacking of molecules by hydrophobic interaction. C10E3-clay composites were characterized by complementary techniques (adsorption isotherms, X-ray diffraction, and infrared spectroscopy) and were compared to benzyldimethyltetradecyl ammonium chloride (BDTAC) cationic surfactant-clay composites for different loadings of the surfactant. For large loadings, the amount of C10E3 adsorbed, which can be described by the Langmuir equation, seemed to reach a steady state close to that of the cationic surfactant. The adsorption processes of the two surfactants were different. For the cationic surfactant, the adsorption, as described in the literature, was due to ion exchange between organic cations and Ca2+ counterions. The adsorption of C10E3 did not depend on electrostatic interaction but rather was due to several interaction mechanisms (H-bonding, ion-dipole, and hydrophobic interaction). For both surfactants, the expansion was limited to two adsorbed monolayers parallel to the clay surface. The expansion of the basal spacing to 17 Å suggested a complete dissociation of the C10E3 lamellar phase when adsorbed on the Ca-smectite. Organo-clays made using the non-ionic surfactant were stable, changing the chemical nature of clay to hydrophobic, and allowing for other cations to be exchanged, which has importance in the manufacture of new nanocomposites or geochemical barriers.

In this study, the feasibility of using surfactant-modified palygorskite (PFl-1) and sepiolite (SepSp-1) for removal of anionic contaminants from water was evaluated from batch experiments. The results showed that both minerals had strong affinity for hexadecyltrimethylammonium (HDTMA), a cationic surfactant used for surface modification. The HDTMA sorption capacities were 520 and 260 mmol/kg for PFl-1 and SepSp-1, respectively. Accompanying HDTMA sorption, the sorption of counterion bromide reached 380, and 210 mmol/kg, for PFl-1 and SepSp-1, respectively, indicating that the sorbed surfactant molecules form admicelles on the minerals’ surfaces. After modification by HDTMA to sorption maxima, these clays showed strong affinity for anionic contaminants such as chromate and nitrate. The chromate sorption capacities were 42 and 34 mmol/kg for HDTMA-modified PFl-1 and SepSp-1, respectively. Desorption of counterion bromide due to sorption of chromate followed a straight-line relationship, suggesting that the sorption of chromate on surfactant-modified palygorskite and sepiolite was also due to anion exchange as with other surfactant-modified clay minerals and zeolites.

Thermally induced lamellar structure changes due to phase transition and degradation in organoclays based on a synthetic ‘Somasif’ mineral and two organic surfactants, di-methyl dihydro-ditallow ammonia chloride (DMDTA) and tri-butyl-hexadecyl phosphonium bromide (HTBP) were investigated by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, in situ simultaneous small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD) over the temperature range 30–280°C. Results indicated that the surfactant layer in ‘Somasif’-based organoclays underwent thermally induced melting-like order-disorder transition followed by desorption of surfactant molecules, resulting in drastic changes in the character of the layer periodicity. The transition temperature (Ttr), determined from the endothermic transition in DSC, was found to depend strongly on the type and the content of surfactant incorporated. Temperature-resolved SAXS indicated complex intercalated layered structures, containing multiple lamellar stack populations of two different organic layer thicknesses. A weak scattering peak (s0), located at exactly the half angular position of the strong first scattering maximum s1 (s0 = 0.5s1), was found in all tested ‘Somasif’ clays. The presence of this peak can be attributed to a slight breaking of the translational symmetry in the layered structure, causing the 1D repeat period in real space to be doubled. In other words, some portions of layers are grouped into pairs and a single pair forms the new repeat unit. This arrangement is reminiscent of the Peierls-like distortion.

The ordering conformation of surfactant molecules in intercalated montmorillonite prepared at various concentrations was investigated by 13C MAS NMR. The 13C MAS NMR study demonstrates the coexistence of ordered and disordered chain conformations. Two main resonance peaks are associated with the backbone alkyl chains: the resonance at 33 ppm corresponds to the ordered conformation (all-trans), and the resonance at 30 ppm corresponds to the disordered conformation (mixture of trans and gauche). Deconvolution of 13C MAS NMR spectra indicates that the ordering conformation of surfactant molecules within the gallery of montmorillonite depends very much on their orientation and packing density. When amine chains are oriented parallel to the silicate layers, the amount of all-trans conformer decreases with the increase of amine concentration. However, the amount of all-trans conformer increases with the increase of amine concentration when amine chains radiate from the silicate layers. Furthermore, 13C MAS NMR spectra show that the intercalated surfactant molecules in the clay minerals never attained the complete liquidlike or solidlike behavior.

Field studies were conducted to evaluate linuron for POST control of Palmer amaranth in sweetpotato to minimize reliance on protoporphyrinogen oxidase (PPO)-inhibiting herbicides. Treatments were arranged in a two by four factorial in which the first factor consisted of two rates of linuron (420 and 700 g ai ha−1), and the second factor consisted of linuron applied alone or in combinations of linuron plus a nonionic surfactant (NIS; 0.5% vol/vol), linuron plus S-metolachlor (800 g ai ha−1), or linuron plus NIS plus S-metolachlor. In addition, S-metolachlor alone and nontreated weedy and weed-free checks were included for comparison. Treatments were applied to ‘Covington’ sweetpotato 8 d after transplanting (DAP). S-metolachlor alone provided poor Palmer amaranth control because emergence had occurred at applications. All treatments that included linuron resulted in at least 98% and 91% Palmer amaranth control 1 and 2 wk after treatment (WAT), respectively. Including NIS with linuron did not increase Palmer amaranth control compared to linuron alone, but it resulted in greater sweetpotato injury and subsequently decreased total sweetpotato yield by 25%. Including S-metolachlor with linuron resulted in the greatest Palmer amaranth control 4 WAT, but increased crop foliar injury to 36% 1 WAT compared to 17% foliar injury from linuron alone. Marketable and total sweetpotato yields were similar between linuron alone and linuron plus S-metolachlor or S-metolachlor plus NIS treatments, though all treatments resulted in at least 39% less total yield than the weed-free check resulting from herbicide injury and/or Palmer amaranth competition. Because of the excellent POST Palmer amaranth control from linuron 1 WAT, a system that includes linuron applied 7 DAP followed by S-metolachlor applied 14 DAP could help to extend residual Palmer amaranth control further into the critical period of weed control while minimizing sweetpotato injury.

In this study, poly(methyl methacrylate-maleic anhydride) (P(MMA-MAh)) was synthesized in toluene from methyl methacrylate (MMA) and maleic anhydride (MAh) monomers via free radical polymerization, in the presence of 2,2′-Azo-bis-isobutyronitrile (AIBN), as initiator at 80ºC for 8 h. The molar ratio of monomers was found to be 1 MAh:8 MMA using hydrolysis and titration. The molecular weight of co-polymer was determined to be of the order of 104 (g/mol) by gel permeation chromatography. The co-polymer was characterized using Fourier transform infrared and nuclear magnetic resonance spectroscopy. Thermogravimetric analysis indicated the initial decomposition temperature was ~270ºC. Differential scanning calorimetry indicated that the glass transition temperature was near 126ºC.

Rectorite modified with benzyldimethyldodecylammonium chloride (OREC) was used as an additive to modify gel polymer electrolytes (GPEs) which consisted of P(MMA-MAh) used as a polymer matrix, propylene carbonate (PC) as a plasticizer and LiClO4 as the lithium ion source. X-ray diffraction analysis indicates that OREC can exfoliate well in GPEs when the amount of clay is suitable. The temperature dependence of the ionic conductivity of the resulting GPEs agreed well with the VTF (Vogel-Tamman-Fulcher) relation. OREC doses of 5 phr resulted in the greatest ionic conductivity. This OREC addition considerably improved the plasticized retention levels. As a consequence of OREC occupying the free volume space in the polymer matrix of GPEs, the bulk resistance of the GPEs was reduced and the glass transition temperature (Tg) increased.

In liquid-filled batteries, the liquid electrolytes may escape or present a fire hazard and an inert spacer is needed to separate the electrodes. Alternative polymer-based electrolytes are of current technological interest. Solid polymer electrolytes are non-volatile, non-corrosive materials, which can readily be processed into any shape or size. However, despite possessing the required mechanical properties, they have inherently lower conductivity. Gel-based systems are an attempt to strike a balance between the high conductivity of organic liquid electrolytes and the dimensional stability of a solid polymer.

Rectorite was modified with dodecyl benzyl dimethyl ammonium chloride to form organic-modified rectorite (OREC). OREC was used as a filler additive to modify gel polymer electrolytes (GPEs) and prepare composite gel polymer electrolytes (CPEs) which consisted of polymethyl methacrylate (PMMA) used as a polymer matrix, propylene carbonate (PC), used as a plasticizer, and LiClO4, used as a lithium ion producer. A variety of physical and chemical techniques was used to characterize the CPEs. The interlayer d spacing of OREC was much larger than that of the initial rectorite (2.22 nm). OREC also possesses a fine microscopic structure, and has a hydrophobic surface. Molau and XRD analysis of CPEs indicate that OREC has good compatibility with the components of CPEs and can be dispersed well. The effects of temperature and OREC dose on properties were studied. The temperature dependence of ionic conductivity of CPEs is well fitted by the VTF (Vogel-Tamman-Fulcher) relation. OREC doses of 5 phr gave the greatest ionic conductivity. This amount also greatly increased the plasticizer maintenance levels. Due to the occupancy of free volume space in the polymer matrix of CPEs by OREC, the bulk resistance of the CPEs was lowered and the glass transition temperature (Tg) increased. The sheet structure of OREC is thought to improve the decomposition temperature of CPEs.

A comparative study using bentonite (BT), hexadecyltrimethylammonium-modified bentonite (BT-HDTMA) and phenyl fatty hydroxamic acid-modified bentonite (BT-PFHA) as adsorbents for the removal of Pb(II) has been proposed. These adsorbents were characterized by X-ray diffraction, X-ray fluorescence, Fourier-transform infrared spectroscopy and surface area measurement. Cation exchange capacity was also determined in this study. The adsorbent capabilities for Pb(II) from aqueous solution were investigated, and the optimal experimental conditions including adsorption time, adsorbent dosage, the initial concentration of Pb(II), pH and temperature that might influence the adsorption performance were also investigated. The experimental equilibrium adsorption data were tested by four widely used two-parameter equations, the Langmuir, Freundlich, Dubinin- Radushkevich (D-R) and Temkin isotherms. The monolayer adsorption capacities of BT, BT-HDTMA and BT-PFHA for Pb(II) were 149.3, 227.3 and 256.4 mg/g, respectively. The experimental kinetic data were analysed by pseudo-first order, pseudo-second order and intraparticle diffusion kinetics models. The experimental data fitted very well with the pseudo-second order kinetic model. Determination of the thermodynamic parameters, ΔG, ΔH and ΔS showed the adsorption to be feasible, spontaneous and exothermic.

Effects of a 28% N solution containing urea and ammonium nitrate (28% UAN) and a nonionic surfactant on efficacy, uptake, and translocation of chlorimuron ethyl ester in soybean and broadleaf weeds were investigated. Chlorimuron applied postemergence at 8.8 and 13 g ai/ha with either nonionic surfactant at 0.25% (v/v), 28% UAN at 9.4 L/ha, or nonionic surfactant plus 28% UAN controlled weeds better than without additives. Chlorimuron with nonionic surfactant and with 28% UAN controlled weeds similarly but with 28% UAN injured soybeans least. Chlorimuron with nonionic surfactant plus 28% UAN controlled velvetleaf best but injured soybeans most. Less than 2% of applied 14C-chlorimuron was absorbed in velvetleaf 84 h after treatment (HAT) when no additive was present, but adding nonionic surfactant, 28% UAN, and nonionic surfactant plus 28% UAN resulted in 21, 9, and 32% uptake, respectively, 84 HAT. Nonionic surfactant plus 28% UAN also increased translocation (primarily acropetal) of the 14C. Adding 28% UAN increased 14C-chlorimuron uptake in velvetleaf grown at low fertility but had no effect under high fertility.

Protoplasts were isolated from quackgrass to investigate the influence of two surfactants and ammonium sulfate on glyphosate uptake. Without adjuvants, the uptake of glyphosate was not detectable. The uptake of the reference compound 2-aminoisobutyric acid was linear with time and was inhibited 60% in the presence of 10 μM carbonyl cyanide m-chlorophenylhydrazone. Glyphosate uptake increased in the presence of both surfactants and ammonium sulfate. After 0.5 h of incubation the internal glyphosate concentration was 37% of the external concentration (100 μM) in the presence of 0.025 g L−1 Ethomeen T/25, 21% in the presence of 0.25 g L−1 Atplus 201, 13% with 5 mM ammonium sulfate, and 20% with 50 mM ammonium sulfate. The surfactant treatments did not reduce either the viability or the internal pH (= 7.1) as judged by fluorescein diacetate staining or 5,5-dimethyloxazolidine-2,4-dione distribution, respectively. The treatments with ammonium sulfate slightly increased the internal pH. The concentration of Ethomeen T/25 required to disrupt the protoplasts was 0.075 g L−1; Atplus 201 did not disrupt the protoplasts at concentrations up to 10 g L−1.

Adjuvants influence weed control and crop tolerance provided by postemergence (POST) herbicides. Adjuvant effects on weed control and corn and soybean tolerance with CGA-248757 and flumiclorac applied alone and soybean tolerance with CGA-248757 and flumiclorac applied in combination with imazethapyr or CGA-277476 were evaluated. Velvetleaf control in the greenhouse and common lambsquarters, redroot pigweed, and common ragweed control in the greenhouse and field with CGA-248757 and flumiclorac were increased by the addition of an adjuvant. However, corn and soybean tolerance to these herbicides was not affected by adding an adjuvant. Laboratory studies suggest enhanced weed control from the addition of an adjuvant resulted from an increase in CGA-248757 and flumiclorac foliar absorption. In greenhouse studies, velvetleaf, common lambsquarters, and redroot pigweed control with CGA-248757 plus imazethapyr; velvetleaf control with flumiclorac plus imazethapyr; redroot pigweed and common ragweed control with CGA-248757 plus CGA-277476; and velvetleaf, redroot pigweed, and common ragweed control with flumiclorac plus CGA-277476 increased by adding an organosilicone adjuvant when compared with adding a nonionic surfactant (NIS). However, in field evaluations of CGA-248757 or flumiclorac plus imazethapyr, the addition of NIS or an organosilicone adjuvant resulted in equivalent soybean injury, common lambsquarters and redroot pigweed control, and soybean yield. Yet in tank mixtures of CGA-248757 or flumiclorac plus CGA-277476, the addition of an organosilicone adjuvant increased redroot pigweed control and soybean yield compared to adding NIS.

Leaves absorbed high amounts of clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) as foliar sprays on honey mesquite (Prosopis glandulosa Torr. # PRCJG) as indicated by concentrations of 10 μg/g fresh wt or more in basal stem phloem by 4 days after treatment. Small quantities of clopyralid (< 1 μg/g) were detected in basal stem phloem after spray applications of clopyralid to defoliated plants or roots treated by soil application. When applied to foliated plants, the 0.56 kg/ha of clopyralid killed 60% or more plants, but none were killed when clopyralid sprays were applied to defoliated plants or when 2.2 kg/ha of clopyralid was applied to the soil. Water, diesel oil plus water, or water plus surfactant were equally effective as clopyralid carriers as foliar sprays.

Research was conducted to determine foliar absorption of 14C-clethodim and its polar degradation products with five adjuvants and to compare the relative herbicidal activity of clethodim and its polar degradation products. Differential 14C-clethodim and 14C-polar degradation products absorption occurred among the five adjuvants. Adjuvants that mediated rapid foliar absorption of clethodim did not always mediate rapid foliar uptake of polar degradation products. Herbicidal activity of clethodim exceeded activity of polar degradation products regardless of time of day of application or whether adjuvant was used. Inclusion of adjuvant was required for herbicidal activity of polar degradation products. Clethodim activity declined when applied at 0800 h EDT compared to applications at 2000 h EDT. To maximize herbicidal activity of clethodim, adjuvants should be selected that mediate rapid foliar absorption of both clethodim and the polar degradation products of clethodim and that minimize photodegradation of clethodim.