Mary H. Wood

Hexadecylamine Adsorption at the Iron Oxide–Oil Interface

The adsorption behavior of a model additive, hexadecylamine, onto an iron surface from hexadecane oil has been characterized using polarized neutron reflectometry, sum-frequency generation spectroscopy, solution depletion isotherm, and X-ray photoelectron spectroscopy (XPS). The amine showed a strong affinity for the metal surface, forming a dense monolayer at relatively low concentrations; a layer thickness of 16 (±3) Å at low concentrations, increasing to 20 (±3) Å at greater amine concentrations, was determined from the neutron data. These thicknesses suggest that the molecules in the layer are tilted. Adsorption was also indicated by sum-frequency generation spectroscopy and XPS, the latter indicating that the most dominant amine–surface interaction was via electron donation from the nitrogen lone pair to the positively charged iron ions. Sum-frequency generation spectroscopy was used to determine the alkyl chain conformation order and orientation on the surface.

Comparative Adsorption of Saturated and Unsaturated Fatty Acids at the Iron Oxide/Oil Interface

A detailed comparison of the adsorption behavior of long straight chain saturated and unsaturated fatty acids at the iron oxide/oil interface has been considered using a combination of surface study techniques. Both depletion isotherms and polarized neutron reflectometry (PNR) show that the extent of adsorption decreases as the number of double bonds in the alkyl chains increases. Sum frequency generation spectroscopic measurements demonstrate that there is also an increase in chain disorder within the adsorbed layer as the unsaturation increases. However, for the unsaturated analogues, a decrease in peak intensity is seen for the double bond peak upon heating, which is thought to arise from isomerization in the surface-bound layer. The PNR study of oleic acid adsorption indicates chemisorbed monolayer adsorption, with a further diffuse reversible adsorbed layer formed at higher concentrations.

Polarized Neutron Reflectometry of Nickel Corrosion Inhibitors

Polarized neutron reflectometry has been used to investigate the detailed adsorption behavior and corrosion inhibition mechanism of two surfactants on a nickel surface under acidic conditions. Both the corrosion of the nickel surface and the structure of the adsorbed surfactant layer could be monitored in situ by the use of different solvent contrasts. Layer thicknesses and roughnesses were evaluated over a range of pH values, showing distinctly the superior corrosion inhibition of one negatively charged surfactant (sodium dodecyl sulfate) compared to a positively charged example (dodecyl trimethylammonium bromide) due to its stronger binding interaction with the surface. It was found that adequate corrosion inhibition occurs at significantly less than full surface coverage.

Anionic Surfactants on Anionic Substrate: Monovalent Cation Binding

Neutron reflectometry has been used to study the adsorption of the anionic surfactant bis(2-ethylhexyl) sulfosuccinate cesium salt on the anionic surface of mica. Evidence of significant adsorption is reported. The adsorption is reversible and changes little with pH. This unexpected adsorption behavior of an anionic molecule on an anionic surface is discussed in terms of recent models for surfactant adsorption such as cation bridging, where adsorption has been reported with the divalent ion calcium but not previously observed with monovalent ions.

Benzylammonium hepta­noate–hepta­noic acid (1/1)

The title salt, C7H10N+·C7H13O2 −·C7H14O2, is an unusual 2:1 stoichiometric combination of two carboxylic acid molecules and one amine. Although there are crystal structures of a number of 1:1 complexes reported in the literature, 2:1 acid amine complexes are rather uncommon. In this case, a proton is transferred between one acid molecule and the amine to give an acid anion and an ammonium cation whilst the other carboxylic acid remains protonated. The species interact strongly via electrostatic forces and hydrogen bonds. In addition we note that the N atom of the ammonium group makes four close contacts to surrounding O atoms. Three of these are hydrogen bonds with neighbouring acid anions while the fourth does not involve a hydrogen atom but is directed towards the carbonyl O atom of the protonated acid. Each of the acid anion O atoms accepts two hydrogen bonds from adjacent N atoms. There is also evidence of short C—H⋯O contacts. There is disorder (occupancy ratio 0.51:0.49) in the alkyl chain of one of the carboxylic acid molecules.

Using Neutron Reflectometry to Discern the Structure of Fibrinogen Adsorption at the Stainless Steel/Aqueous Interface.

Neutron reflectometry has been successfully used to study adsorption on a stainless steel surface by means of depositing a thin steel film on silicon. The film was characterized using XPS (X-ray photoelectron spectroscopy), TOF-SIMS (time-of-flight secondary ion mass spectrometry), and GIXRD (grazing incidence X-ray diffraction), demonstrating the retention both of the austenitic phase and of the required composition for 316L stainless steel. The adsorption of fibrinogen from a physiologically-relevant solution onto the steel surface was studied using neutron reflectometry and QCM (quartz crystal microbalance) and compared to that on a deposited chromium oxide surface. It was found that the protein forms an irreversibly bound layer at low concentrations, with maximum protein concentration a distance of around 20 Å from the surface. Evidence for a further diffuse reversibly-bound layer forming at higher concentrations was also observed. Both the structure of the layer revealed by the neutron reflectometry data and the high water retention predicted by the QCM data suggest that there is a significant extent of protein unfolding upon adsorption. A lower extent of adsorption was seen on the chromium surfaces, although the adsorbed layer structures were similar, suggesting comparable adsorption mechanisms.

(S)-(-)-1-Phenyl-ethanaminium hexa-noate.

A binary mixture of (S)-(−)-1-phenylethanamine and hexanoic acid was allowed to react to form the title salt, C8H12N+·C6H11O2 −. This crystal contains a 1:1 stoichiometric mixture of the acid- and amine-derived species and displays a chiral structure with N—H⋯O hydrogen-bonded chains propagating along the c-axis direction.

Characterizing Surfaces of Garnet and Steel, and Adsorption of Organic Additives

This work reports that abrasive blasting of a structural steel results in significant retention of garnet abrasive residues. A comparative study of the adsorption behavior of a number of organic species, relevant to paint components and additives, onto the surfaces of garnet and S355 steel from nonaqueous solutions is also presented. Areas per adsorbed molecule, estimated from the isotherm data, suggest a range of molecular orientations on the surfaces. Pronounced differences in the adsorption strength to the garnet and steel were observed, particularly that most additives bind more strongly to steel than to garnet. Surface characterization data from acid-base titrations, photoelectron spectroscopy, and backscattered electron diffraction were used to rationalize the adsorption data obtained. The ramifications of these findings for particular industrial processes, with regards the strength of paint adhesion and paint additive formulations, are highlighted.

An X-ray and neutron reflectometry study of iron corrosion in seawater

The corrosive breakdown of thin iron films supported on silicon substrates under a number of conditions is presented-in particular to understand better how iron, and hence ferritic steel, behaves in a salty water environment. A combination of X-ray and neutron reflectometry was used to monitor the structures of both metal and oxide surface layers and also organic corrosion inhibitors adsorbed at the iron/aqueous interface. A range of behavior in seawater was observed, including complete dissolution and void formation under the metal surface. Importantly, two simple treatments-UV/ozone or soaking in ultrapure water-were found to significantly protect the iron surface for considerable lengths of time, although evidence of pitting corrosion began after around 10 days. The underlying causes of the efficacies of these treatments were further investigated using X-ray photoelectron spectroscopy. In addition, three potential corrosion inhibitors were investigated: (i) dodecyltrimethylammonium bromide (DTAB) demonstrated no ability to protect the surface; (ii) sodium dodecyl sulfate (SDS) appeared to accelerate corrosion; and (iii) bis(2-ethylhexyl)phosphate showed an impressive level of protection (the neutron reflectometry results indicated a thick diffuse layer of surfactant of 23% surface coverage). These findings have been interpreted in terms of preferential inhibitor adsorption at cathodic and anodic surface sites (depending on the nature of the inhibitor).

Bovine Serum Albumin and Fibrinogen Adsorption at the 316L Stainless Steel/Aqueous Interface

The binding of bovine serum albumin (BSA) to a 316L stainless steel surface from a buffer solution has been characterized using neutron reflectometry and quartz crystal microbalance measurements; coverage at all concentrations up to a near-physiological concentration was found to be relatively low (<20%); the protein followed a two-step isotherm adsorption model type and the overall thickness at the higher concentrations (around 80 Å) suggested possible multilayering and/or protein unfolding. As it has been postulated that BSA may inhibit the further adsorption of another blood plasma protein-fibrinogen-the effects of preadsorbing BSA on fibrinogen adsorption were examined, first by prior physisorption of BSA to the stainless steel surface and second by pretreating the stainless steel with a layer of sodium dodecyl sulfate (SDS) to render it more hydrophobic. Although the preadsorption of BSA to an untreated stainless steel surface did slightly decrease the amount of fibrinogen adsorbed initially, it had no inhibiting effect if a solution containing solely fibrinogen subsequently flowed through. In contrast, the SDS-treated surface yielded both an increased BSA adsorption and consistently decreased fibrinogen adsorption.