Self organization of granular flow by basal friction variation: Natural jump,moving bore,and flying avalanche

The article discusses the response of rapid granular downslope flow to an abrupt change in basal friction. Although granular discharge from silo and hoppers has received considerable attention in the past, the flow behavior for an abrupt change in basal friction is hitherto unexplored. In the present study, the channel floor comprises of a smooth surface (bed friction angle—δ_S) and a rough surface (bed friction angle—δ_R) such that the angle of repose of the granular material (θ_r) lies between δ_S and δ_R and the flow features are observed as the channel inclination (θ) is varied from ≈δ_S to >δ_R. Experiments are performed in two channels with different extent of rough surface for two grain sizes with the same angle of repose and different inlet depth of granular flow. The visualization studies reveal a rich variety of flow features namely moving bore, rapid granular flow, flying avalanche and granular jump. Natural granular jump formed by mere frictional dissipation without any external forcing has not been reported earlier. The variety of flow features primarily results from the interplay of downslope motion of variable depth, collision-driven piling of grains, and slope shaving avalanches. The observed flow phenomena have been satisfactorily analyzed by the well-known depth-averaged avalanche flow equations under conditions of incompressible granular flow.     

The limiting pressure-velocity (PV) of plastics under unlubricated sliding

The limiting pressure-velocity (PV) of plastics materials under normal contacting pressure P and sliding velocity V when the sliding goes on continuously unlubricated has been discussed theoretically in this study. The sliding friction tests between the rotating edge of a hollow cylinder against a stationary metal surface were carried out in room air and when the metals were cooled with circulating water. The results obtained were as follows:

• The relation between PV_max and the critical temperature τ_bmax of the surface above which ordinary frictional conditions are not maintained may be represented by the following formula, Where C = Hn/μk, and H is the mean total heat conductivity between materials and environment in cal/cm². °C · s, n the area ratio of heat radiation surface to frictional surface, μ the kinetic frictional coefficient, k the thermal equivalent of frictional work in cal/kg · cm · s, and τ_a the cooling or environment temperature.
• The value of C ranges from 1 to 10 in cal/kg · cm s · °C, and the value of PV_max from 45 to 750 in kg/cm² · cm/s under prevailing room temperature air cooling in this experiment, however, the value of C has been increased about 2.3 times as much as those values by circulating water of 2°C around the lower side of the test piece.

     

Role of hydrophobic bonding in the contraction of nylon 66 in phenolic solutions

Rate constants for intermolecular bond breaking (k₁) and bond re-formation (k₂) were calculated from contraction measurements. Variation of ΔH? and ΔS? for k₁ with phenol substituents and concentration suggests the existence of hydrophobic bonding between the solution and the polymer activated complex. This behavior has been substantiated by correlating ΔH? and ΔS? for k₁ with a parameter related to hydrophobicity.     

Activity of Bromelain with Cationic Surfactants and the Correlation with the Change of 1H NMR Signals

This study observed the activities of bromelain in the presence of various cationic surfactants at different temperatures and the conformational changes in bromelain by ¹H NMR spectroscopy. We found that the bromelain activity was enhanced by tens to hundreds of micromoles per liter of the surfactant. In the presence of the surfactants, bromelain exhibited good tolerance to a range of substrate temperatures and its thermal stability was also increased. The ¹H NMR experiments indicated that when the temperature was increased from 25.0 to 45.0 °C, the protons of bromelain having chemical shifts (δ) between 3.7 and 5.2 ppm moved upfield, while those having δ values between 3.2 and 3.7 ppm moved downfield. In the bromelain/cationic surfactant mixture, the values of δ for the protons in both bromelain and the cationic surfactants decreased, accompanied by the broadening of the half-peak width of the surfactant protons. These results indicated that both increasing temperature and adding a cationic surfactant made the bromelain chain more flexible and hence, increased the bromelain activity. To the best of our knowledge, this was the first time that the relationship between the protein activity and the ¹H NMR data was expounded.     

Surface interaction of quaternary amines with hair

Surface analysis by X-ray photoelectron spectroscopy (XPS) has shown specific 1∶1 (ionic) interaction between cationic alkyl quaternary surfactant molecules and the anionic sulfonate groups present on the hair surface. The primary driving force for the adsorption of alkyl quaternary amine molecules to the surface of the hair from aqueous solution is the ionic interaction between quaternary groups and the surface SO₃ ⁻ on the hair. Cationic quaternary molecules incorporating ester and alcohol functionalities (ester quats) demonstrate a lower number of surface quaternary nitrogens per sulfonate group, indicating an altered surface interaction mechanism. For the ester quats, a combination of electrostatic interaction modes exists in addition to the ionic N⁺/SO₃ ⁻ interaction, specifically, H-bonding interactions of the −C−O, −C−OH, and −C(O)O− polar groups with SO₃ ⁻ and other polar groups on the hair. Surface coverage of the ester quat is not reduced despite the decrease in ionic interaction at the surface. Both types of molecules orient their alkyl tails toward the surface. Molecular dynamics modeling of the surfactant/hair surface interaction indicates higher adsorption energies due to increased dipolar interactions for ester quat molecules.     

Investigation of Mixing Behavior of both a Conventional Surfactant and Different Inorganic Salts with a Cationic Gemini Surfactant in Aqueous Solution

N,N′-bis [3-(dodecanoylamino)propyl]-N,N,N′,N′-tetramethylhexane-1,6-diaminium dibromide is a cationic Gemini surfactant including quaternary ammonium salt with amide groups. Critical micelle concentration (CMC) and some thermodynamic parameters of the cationic Gemini surfactant were investigated using surface tension and conductivity methods. Mixed micellization of binary mixtures of the cationic Gemini surfactant with a conventional surfactant cetyl trimethylammonium bromide (CTAB) was investigated using the conductometric method at five different temperatures ranging from 303.15 to 323.15 K. CMC, micellar ionization degree (α_m), counterion binding constant (g₁), interaction parameter (β), and activity coefficients ( and ) of mixed systems were found out from data of conductivity at different mole fractions for all studied temperatures. Additionally, the effects of some inorganic salts with different concentrations on the surface properties of cationic Gemini surfactant were examined by surface tension measurements. Some surface properties of the pure cationic Gemini surfactant and mixed salts systems were calculated using the data of surface tension.     

Corrosion Inhibition Efficiency,Electrochemical and Quantum Chemical Studies of Some New Nonionic Surfactants for Carbon Steel in Acidic Media

In this work, three types of nonionic surfactant as corrosion inhibitors were synthesized. The chemical structure of the prepared inhibitors was confirmed using FT‐IR and ¹H‐NMR spectroscopy. The surface tension and thermodynamic properties of these inhibitors were investigated. The corrosion inhibition efficiency of these surfactants was investigated on a carbon steel surface in 1 M HCl solution by weight loss and electrochemical measurements. Untreated and treated steel surfaces were characterized by scanning electron microscopy. Results show that the inhibition efficiency of the prepared inhibitors increases with increasing the ethylene oxide units. Also, the potentiodynamic polarization curves indicated that the investigated inhibitors behave as a mixed type inhibitor. Adsorption of these surfactants on the carbon steel surface was found to obey Langmuir's adsorption isotherm. The computed quantum chemical properties viz., electron affinity (EA), highest occupied molecular orbital (E_HOMO), the lowest unoccupied molecular orbital (E_LUMO), energy gap ΔE = E_HOMO ? E_LUMO, dipole moment (μ), polarizability and total energy (E_T) show good correlation with experimental inhibition efficiency.     

Effects of cationic liposome-DNA complexes on pulmonary surfactant function in vitro and in vivo

Cationic liposome-DNA complexes are being evaluated as potential gene therapy agents for the lung. Cations have strong effects on the biophysical functions of lung surfactant. Therefore, we assessed whether cationic liposomes [composed of N-(1-(2,3-dioleyloxy) propyl)-N,N,N-trimethyl-ammonium chloride and dioleylphosphatidylethanolamine] with or without DNA affect behavior of four types of surfactant in vitro. Experiments were carried out using a modified Wilhelmy surface balance. The ability of surfactants that contain protein and anionic lipids to lower surface tension was inhibited in the presence of cationic liposomes. Inactivation was less when DNA was preincubated with cationic liposomes. Surfactant that contained neither protein nor anionic lipids was not inactivated. Mechanical properties of the lung were studied to assess in vivo surfactant function after intratracheal instillation of a cationic liposome-DNA complex into adult rats. Pressure-volume deflation curves were shifted by 18% compared with those from normal (untreated) animals, but this effect was transient and not different from that observed in animals who received a similar volume of saline. These findings indicate that cationic liposomes alone may have deleterious effects on behavior of some surfactants possibly by disrupting charge interactions between negatively charged phospholipids and surfactant proteins. When DNA is added to liposomes before exposure to surfactants, the adverse charge interactions may be obviated by charge neutralization of liposomes by DNA.     

A Comparative Study on the Aggregation and Thermodynamic Properties of Anionic Sodium Dodecylsulphate and Cationic Cetyltrimethylammonium Bromide in Aqueous Medium: Effect of the Co-solvent N-Methylacetamide

The effect of co‐solvent N‐methylacetamide (NMA) (0.035, 0.046, 0.127, and 0.258 mol kg^?1) on the micellization behaviour of anionic surfactant sodium dodecylsulphate (SDS) (3.21–10.35 mmol kg^?1) and cationic surfactant cetyltrimethylammonium bromide (CTAB) (0.19–3.72 mmol kg^?1) in aqueous solution was explored by employing conductivity measurements at different temperatures (298.15–313.15 K). The critical micelle concentration (CMC) values for SDS and CTAB in aqueous solutions of NMA were determined from the conductivity versus surfactant concentration plots. The variations in the CMC values of SDS with NMA concentration are in striking contrast to those observed in the case of CTAB. The various relevant thermodynamic parameters of micellization, viz. standard enthalpy change, ΔH_m^o, standard entropy change, ΔS_m^o, and standard Gibbs free energy change, ΔG_m^o, were determined using the temperature variation of the CMC values and counterion binding. The results not only relate these thermodynamic parameters to the consequences of intermolecular interactions but are also able to differentiate between SDS–water–NMA and CTAB–water–NMA systems in terms of contributions from head groups as well as alkyl chains of surfactants.     

Preparation of soap‐free cationic emulsion using polymerizable surfactant

A kind of polymerizable surfactant, methacryloyloxyethylhexadecyldimethylammonium bromide (DMHB) was used to synthesis soap‐free cationic emulsion with styrene (St), methyl methacrylate (MMA), and methacryloyloxyethyltrimethylammonium chloride (MATMAC) by emulsion polymerization using 2,2′‐azobis(isobutylamidine hydrochloride) (AIBA) as a cationic initiator. The effects of polymerizable surfactant concentration, initiator concentration, and reaction temperature on the conversion of monomer were investigated. The results indicated that the rate of polymerization could be expressed as R_p = k_p[AIBA]^0.42[DMHB]^0.45 and the apparent activation energy (E_a) was 83.42 kJ/mol. The particle size, ζ potential, and apparent charge density of cationic latices were also measured. The average diameter of copolymer particles decreased with increasing DMHB, MATMAC, and AIBA content; the charge properties of the particles were decided by the DMHB, MATMAC, and AIBA content. The polymerization mechanism is discussed. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1111–1116, 2006     

Electrokinetic properties of polyformaldehyde fibers

Electrokinetic properties, namely, zeta potential (ζ), surface charge density (σ), and surface conductivity (K_s) of polyformaldehyde fibers [poly(oxymethylene) fibers] have been studied in the presence of direct dyes, with or without surfactants and an electrolyte. The anionic dyes increased the negative zeta potential of fibers. The increase in ζ was found to be a function of concentration and basicity of the dye in the streaming solution. Thus, the tetrabasic dye gave higher value of negative ζ than the equivalent concentration of the dibasic dye. The cationic surfactant brought about a decrease in negative ζ, giving a point of inflection, while the anionic surfactant increased it. The nonionic surfactant brought about a certain reduction in negative ζ, but failed to give a point of inflection. In the presence of a direct dye, the cationic surfactant brought about considerable reduction in negative ζ, to give a point of inflection. The presence of an electrolyte in the streaming dye solution progressively lowered the negative ζ. In general, σ increased with the increase in the concentration of either a dye or an electrolyte in the presence of a given concentration of the dye in the streaming solution. Results on K_s indicated that the surface conductivity of the fibers is a function of concentration of dye, surfactant, and electrolyte. It was, however, observed to be independent of the nature of the surfactant. Although both the dibasic and tetrabasic direct dyes brought about an increase in K_s, the extent of increase was dependent upon the basicity of the molecules.     

Hydrogen-Atom Transfer Oxidation with H2O2 Catalyzed by [FeII(1,2-bis(2,2′-bipyridyl-6-yl)ethane(H2O)2]2+: Likely Involvement of a (μ-Hydroxo)(μ-1,2-peroxo)diiron(III) Intermediate

The iron(II) triflate complex ( 1 ) of 1,2-bis(2,2′-bipyridyl-6-yl)ethane, with two bipyridine moieties connected by an ethane bridge, was prepared. Addition of aqueous 30 % H₂O₂ to an acetonitrile solution of 1 yielded 2 , a green compound with λ_max=710 nm. Moessbauer measurements on 2 showed a doublet with an isomer shift (δ) of 0.35 mm/s and a quadrupole splitting (ΔE_Q) of 0.86 mm/s, indicative of an antiferromagnetically coupled diferric complex. Resonance Raman spectra showed peaks at 883, 556 and 451 cm⁻¹ that downshifted to 832, 540 and 441 cm⁻¹ when 1 was treated with H₂¹⁸O₂. All the spectroscopic data support the initial formation of a (μ-hydroxo)(μ-1,2-peroxo)diiron(III) complex that oxidizes carbon-hydrogen bonds. At 0 °C 2 reacted with cyclohexene to yield allylic oxidation products but not epoxide. Weak benzylic C−H bonds of alkylarenes were also oxidized. A plot of the logarithms of the second order rate constants versus the bond dissociation energies of the cleaved C−H bond showed an excellent linear correlation. Along with the observation that oxidation of the probe substrate 2,2-dimethyl-1-phenylpropan-1-ol yielded the corresponding ketone but no benzaldehyde, and the kinetic isotope effect, k_H/k_D, of 2.8 found for the oxidation of xanthene, the results support the hypothesis for a metal-based H-atom abstraction mechanism. Complex 2 is a rare example of a (μ-hydroxo)(μ-1,2-peroxo)diiron(III) complex that can elicit the oxidation of carbon-hydrogen bonds.     

Enhancement of enzymatic catalysis of Bacillus amyloliquefaciens α-amylase by nonionic surfactant micelles

Some enzymes are considerably more stable when formulated with nonionic surfactants than when formulated with anionic surfactants. The effect of a nonionic surfatant, polyoxyethylene mono-N-dodecyl ether (Brij 35; number of units of ethylene oxide moieties, 23), on the kinetic behavior of hydrolysis of amylopectin with Bacillus amyloliquefaciens α-amylase (BAA) was studied at a temperature of 25°C and a pH of 7.0. The hydrolytic rate was accelerated by the addition of the nonionic surfactant above its critical micelle concentration. Lineweaver-Burk plots for the enzymatic hydrolysis in the absence and presence of the nonionic surfactant at 0.5 to 2.5% (wt/vol) had linear relationships, and the kinetic parameters, K _m and k _cat were obtained. The value of k _cat was increased with an increased concentration of Brij 35, whereas the K _m value was approximately constant. Therefore, the increase in k _cat contributed to the acceleration of the apparent hydrolytic rate. The interaction of amylopectin with the surfactant was examined by a surface tension measurement, and the result confirmed the corresponding binding between the substrate and the surfactant. A fluorescence analysis due to tryptophan in BAA suggested that BAA bound to the nonionic micelles. The increase in k _cat suggested that hydrolytic catalysis at the micellar pseudophase was more efficient than that at the aqueous pseudophase. The enhancement of the catalytic rate contributed to the effective removal of food stains containing starch when BAA was added with Brij 35 in a laundry detergent washing test.     

Extraction of Rare Earth Metals Using Liquid Surfactant Membranes Prepared by a Synthesized Surfactant

Abstract

Three surfactants, l-glutamic acid dioleyl ester ribitol (nonionic, 2C ₁₈Δ⁹ GE), l-glutamic acid dioleyl ester quaternary ammonium chloride (cationic, 2C ₁₈Δ⁹ GEC ₂ QA), and dioleyl dimethyl quaternary ammonium chloride (cationic, 2C ₁₈Δ⁹ QA) were synthesized for potential use in liquid membrane operations. These surfactants have strongly hydrophobic, twin oleyl chains as the hydrophobic moiety. Using the synthesized surfactants, extraction of rare earth metals was carried out by liquid surfactant membranes in a stirred tank. The extraction behavior of 12 kinds of rare earth metals was systematically studied with 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester (commercial name: PC-88A) as a carrier. Different surfactants having an identical hydrophobic moiety can have significantly different behaviors in rare earth extractions by liquid surfactant membranes, where extraction efficiency appears to be governed by the nature of the interfacial microenvironment between oil and water. An interfacial reaction model which takes into account the adsorption of a surfactant at the interface has been proposed to evaluate the permeation rate of rare earth metals by liquid surfactant membranes. It was found that a cationic surfactant strongly enhances the extraction rate of rare earth metals compared with the conventional surfactant, Span 80. The cationic surfactant 2C ₁₈Δ⁹ GEC ₂ QA appears to be one of the best surfactants currently available for rare earth extraction by liquid surfactant membranes.     

Performance characteristics of air intake pleated panel filters for internal combustion engines in a two-stage configuration

Previous numerical studies that have used computational fluid dynamics (CFD) and experimental software to address the effects of the geometric parameters of pleats on the pressure drop and air flow rate through a fibrous filter are analyzed. The analysis establishes that using a test dust with gradually smaller particle sizes (10, 5, and 1?μm) results in a more intense increase in the filter pressure drop, thus decreasing the service life of the filter. The benefits of using a multicyclone as the first stage of air filtration are discussed. Selecting the air filter by determining the active surface of the filter medium A_c based on the allowable filtration rate is not sufficient; to select the filter medium of a motor vehicle air filter, the dust mass retained per unit of filtration area (mass loading of dust k_m) must be known for a specific allowable pressure drop Δp_fdop. New methods and conditions for determining the mass loading of dust k_m for filter paper and non-woven fabric in single-stage and two-stage filtration systems are presented. The characteristics of the separation efficiency and filtration performance as well as the pressure drop of a filter set comprising a single cyclone and a filter element with a specific filter medium surface are determined. The effects of the particle size distribution of the dust in the air downstream of the cyclone on the mass loading of dust k_m of the filter paper and non-woven fabric in a two-stage filtration system are presented. The mileage of a truck fitted with a single-stage or two-stage filtration system in a “multicyclone–panel filter” configuration is estimated based on the calculated mass loading of dust k_m of the filter paper and non-woven fabric.

© 2018 American Association for Aerosol Research     

Experimental study of surfactant driven nematic liquid crystal (NLC) anchoring transitions at solid surfaces: role of solid surface energy and anisotropic NLC – solid interfacial energy

The fundamental understanding of nematic liquid crystal (NLC) alignment on solid surfaces is significant for the operation of liquid crystal displays and devices. We investigate the effect of structure and concentration of surfactants on the anchoring of NLC 4-cyano-4′-pentylbiphenyl (5CB) at 5CB–solid interface. 5CB molecules undergo an ordering transition from parallel to normal anchoring near the surfactant critical micelle concentration depending on the chemical structure of the surfactant tails. In contrast to the previous studies which point to the solubilization of 5CB in surfactant micelles, our experiments indicate that NLC anchoring transition occurs due to the ability of 5CB molecules to penetrate into the surface surfactant layer. The surfactant-driven 5CB anchoring is further related to the surface tension of 5CB (γ_5CB), surfactant adsorbed substrate surface energy (γ_sa), anisotropic 5CB–surface interfacial energy (Δγ_sl), and spreading coefficient (S). Our experimental results agree with the Creagh–Kahn criterion of predicting surface anchoring from relative values of γ_sa and γ_5CB. A change in the sign of Δγ_sl and S is also observed along with the anchoring transition. Using a semi-empirical approach, we show that dipolar interactions dominate over dispersion interactions when 5CB molecules exhibit perpendicular anchoring at the solid–5CB interface.     

Surfactant Effects on Aeration Performance of Stirred Tank Reactors

The effect of surfactants on aeration performance in stirred tank reactors (STR) at high rates of foaming is studied. The volumetric oxygen transfer coefficient (k_La) and foaming activity estimated as foaming height (H_f) were determined. Biotechnology of lipopeptide biosurfactants from aerobic organisms, e.g., Bacillus subtilis were addressed. Using model solutions of known foam‐generating properties, high‐molecular weight surfactin and low‐molecular weight sodium dodecyl sulphate (SDS), as well as impellers of different types, with flat and fluid‐foil blades, clues on the concentration dependence of STR oxygen transfer and foaming as well as options for foam reduction in the presence of biosurfactant were sought. In response to a two‐fold decrease of surface tension by surfactin, k_La values decreased up to 30 % but remained within the range expected for the mixing system in water; the experiments with SDS showing stronger dependence on surfactant concentration and surface tension. Mixing of surfactant media by a standard six‐blade disc turbine (RT) imposed rate limitations on gassing. A low‐shear impeller Narcissus (NS) could be used to avoid bulk foam outflow, while preserving k_La values that remained unchanged. The ‘power per unit volume' correlation of k_La in stirred tanks is tested in the presence of surfactin.     

Synthesis and Physico-Chemical Properties of Sodium 3-Oxo-2-(3-(4-sulphonatophenyl)triaz-2-enyl)octadecanoate Anionic Surfactant

The novel anionic surfactant sodium 3‐oxo‐2‐(3‐(4‐sulphonatophenyl)triaz‐2‐enyl)octadecanoate (SSTO) was prepared from renewable raw materials; glycine and palmitic acid. Surface and bulk properties of SSTO were investigated by surface tension and electrical conductivity techniques at 298, 308, 318 and 328 K. Surface properties including critical micelle concentration (CMC), maximum surface excess concentration (Γ_max), minimum area per molecule (A_min), surface tension at CMC (γ_CMC), effectiveness of surface tension reduction (Π_CMC), efficiency of surface adsorption (pC₂₀), and degree of counterion dissociation (α) were determined. The thermodynamic parameters of micellization (ΔG°_mic, ΔH°_mic and ΔS°_mic) and adsorption (ΔG°_ad, ΔH°_ad and ΔS°_ad) were also investigated at 298, 308, 318 and 328 K. The effect of 3 wt% n‐propanol, n‐butanol and n‐pentanol on surface tension and conductivity at 298 K was also determined.     

Carbon Dioxide Absorption into Stirred Emulsions of n‐Alkanes

Volumetric mass transfer coefficients k_La for CO₂ absorption into n‐alkane/water emulsions were determined at oil volume fractions of 0–100 % in a stirred tank at a stirring speed of 1000 min^?1. The oil was n‐heptane, n‐hexadecane, or n‐dodecane. The decrease of k_La with increasing volume fraction of dispersed oil can be uniformly correlated to the emulsion viscosity with the power of ?0.72. Only the addition of n‐heptane caused a strong increase of the mass transfer coefficient. Upon addition of the surfactant sodium dodecyl sulfate to n‐heptane emulsions, k_La decreased as for the other oils. The increase can therefore be attributed to the spreading of n‐heptane on the bubble surface enabling gas‐oil contact, whereas spreading is inhibited by the ionic surfactant.     

Molecule structure variations in friction of stainless steel/PTFE and its composite

The friction and wear characteristics of PTFE and one of its composites, JS material rubbing against stainless steel, were determined with a pin-disk tester in this study. The JS material is a multilayer composite composed of PTFE layer containing metal oxide and others, porous bronze layer, copper-plating layer and steel back. The submicroscopic features of frictional surfaces of stainless steel and JS materials were observed with an electron probe microanalyzer (EPM). By analysis of fractional surfaces of stainless steel pins in various operating stages with X-ray photoelectron spectroscopy (XPS), chemical shifts of C_ls, O_ls, and F_ls peaks, F-ion gathering in surface transfer films, and generation of a metal fluoride and an unknown compound containing oxygen were found. The determination of JS material wear debris with electron spin resonance spectroscopy (ESR) showed that polymeric radicals different in structure and stable in air existed. The authors consider that these PTFE molecule structure variations might be of benefit to the adhesion of PTFE transfer film to the rubbed stainless steel surface, which is important to improve the friction and wear performance of PTFE.