Adsorption characteristics of various organic substances on the surfaces of tantalum, titanium, and zirconium

Adsorption characteristics of carboxylic acids, amines, an octapeptide composed of four L-alanine and four L-aspartic acid residues (Peptide-A4D4), and beta-lactoglobulin (beta-Lg) on tantalum (Ta), titanium (Ti), and zirconium (Zr) particles were examined at 30 degrees C and in some case, were compared with their adsorption onto SUS316L stainless steel particles (S6L). The adsorption isotherms on the Ta, Ti, and Zr particles could usually be expressed either by a Langmuir-type equation for reversible adsorption or by a modified Langmuir-type adsorption equation including terms for both reversible and irreversible adsorption. The adsorption equilibrium of benzoic acid, benzylamine, and m-xylylenediamine on all the metal surfaces followed a Langmuir-type equation, while those of phthalic acid, mellitic acid, and Peptide-A4D4 could be fitted to the modified Langmuir-type adsorption equation. The adsorption characteristics of different adsorbates on the different surfaces were discussed particularly with reference to the pH dependencies of the q(irrev), q(rev), and K values and the electrostatic properties of the oxidized surface of the metal particles. Fourier transform infrared spectroscopic analyses using a reflection/absorption technique (RA-IR) indicated that phthalic acid and mellitic acid are adsorbed in similar adsorption states irrespective of the type of metal. beta-Lg was adsorbed onto the surfaces principally in an irreversible manner. The desorption behavior of beta-Lg from Ta, Ti, and S6L surfaces was examined, in order to evaluate the extent of interaction between beta-Lg and the metals.     

Adsorption Behavior of Amino Acids on a Stainless Steel Surface

The adsorption behavior of various amino acids on a stainless steel surface was investigated at 30 degrees C and over a pH range of 3-10. Acidic and basic amino acids except histidine adsorbed remarkably at pH 3-4 and 7-10, respectively, and showed Langmuir-type adsorption isotherms. The effects of pH and ionic strength on the adsorption isotherms were investigated to analyze the interactions between amino acids and adsorption sites on the stainless steel. Hydrophobic amino acids and glycine showed only small adsorbed amounts at all pHs tested. For the acidic and basic amino acids, reversibility of the absorption and the influence of the ionic strength on the adsorption behavior were examined. The adsorption isotherms of the derivatives of aspartic acid were also measured in order to examine the contribution of the carboxylic groups of acidic amino acids to the adsorption. Furthermore, a Fourier-transform infrared spectroscopic analysis and semiempirical molecular orbital calculation were carried out to analyze the ionization states and the configuration of the amino acids adsorbed on a stainless steel surface. These investigations suggest that the acidic and basic amino acids adsorb through two electrostatic interactions of two ionized groups in the amino acid with a stainless steel surface. Copyright 2000 Academic Press.     

Adsorption behavior of methylene blue and its congeners on a stainless steel surface

Methylene blue and its congeners as model dyes were adsorbed onto stainless steel particles at different ionic strengths, pH values, and ethanol contents, and the adsorption mechanism was investigated. A Fourier transform infrared spectroscopy (FTIR) analysis of the dyes adsorbed on the stainless steel plate was carried out to determine the orientations of the adsorbed dyes on stainless steel surface. The adsorption isotherms for all the dyes tested were approximated by a Langmuir equation (Q=Kq(m)C/(1+KC)) in most cases except under strongly basic conditions. From the ionic strength and ethanol content dependencies of the K value in the Langmuir equations, both the electrostatic and hydrophobic interactions were indicated to contribute to the adsorption of the dyes at neutral pH. By comparing the K and q(m) values for the methylene blue congeners and with the aid of the FTIR analyses, it was found that the kind of substituent groups at most positions of the polyheterocycles of methylene blue strongly affects the adsorption behavior, particularly the area occupied by an adsorbed dye molecule, the affinity for the stainless steel surface, and the orientation of the adsorbed dye molecule on the stainless steel surface.     

Contribution of acidic amino residues to the adsorption of peptides onto a stainless steel surface

The role of the acidic amino acid residues in the adsorption of peptides/proteins onto stainless steel particles was investigated using a peptide fragment from bovine beta-lactoglobulin, Thr-Pro-Glu-Val-Asp-Asp-Glu-Ala-Leu-Glu-Lys (T5 peptide), which has a high affinity to a stainless steel surface at acidic pHs, and its mutant peptides substituted with different numbers of acidic amino acid residues. The adsorption behavior of the mutant peptides as well as the T5 peptide were studied at pH 3 with respect to concentration and ionic strength dependencies and the reversibility of the adsorption process. The behavior of the peptides was generally characterized as two distinct irreversible adsorption modes, Mode I and Mode II. In Mode I, the amounts adsorbed lay on the ordinate at zero equilibrium concentration in the solution, while in Mode II, the amount adsorbed increased with increased equilibrium concentration. The area occupied by the peptides was predicted by molecular mechanics and molecular dynamics. The state of the peptides, when adsorbed, was investigated using FT-IR analysis. The FT-IR analyses revealed that the side carboxylic groups of the peptides adsorbed on the stainless steel surface were ionized, while they were unionized in the solution at pH 3. Thus, the interactions between the carboxylic groups of the peptide and the stainless steel surface can be considered to be largely electrostatic. The peptide having four acidic amino acid residues took a maximum adsorbed amount, the reason for which is discussed.     

碱性介质中L-赖氨酸在纳米金膜电极上的吸附和氧化过程

采用原位红外反射光谱(in situ FTIRS)和循环伏安法(CV)研究了碱性介质中L-赖氨酸在纳米金膜电极(nm-Au/GC)上的解离吸附和氧化过程. 研究结果表明, 在碱性溶液中以阴离子形式存在的赖氨酸[-OOC—CH—NH2—(CH2)4—NH2]在低电位区间(-0.95~-0.80 V, vs. SCE)发生部分解离, 生成AuCN-物种(约2110 cm-1), 同时赖氨酸阴离子的羧基侧还可通过两个氧原子与金电极表面相互作用. 随着电位的升高, 吸附态CN-氧化产生NCO-, OCN-和AuCN, 其对应的红外吸收峰分别位于2254, 2168和2226 cm-1附近.     

Adsorption isotherm and atomic force microscopy studies of the interactions between polymers and surfactants on steel surfaces in hydrocarbon media

The adsorption isotherms for certain polymer and surfactant molecules (and in some cases their mixtures) on stainless steel beads from isooctane have been obtained, together with corresponding adsorbed layer thicknesses, using an atomic force microscope. The polymer is a terminally functionalised (ethylene diamine), low molecular weight polyisobutylene (PIB) derivative and the surfactants are basically alkyl or alkyl phenol alkoxylate molecules, which in one case has been derivatised with an amino functionality. The results indicate the presence of multilayers at the stainless steel-isooctane interface. Theoretical analysis of the surfactant adsorption isotherms suggests molecular aggregation at the interface with an aggregation number between 2 and 6, at the highest coverages. The adsorption of the polymer is reduced in the presence of the surfactant molecules. The polymer leaches metal ions from the steel surface at higher concentrations.     

Wetting and adsorption: II. Adsorption of Triton X-100 and Triton X-305 onto carbon black from water and cyclohexane solutions

The adsorption isotherms of nonionic surfactants Triton X-100 and Triton X-305 from water and cyclohexane on carbon black have been determined at 15 and 30°C. The Langmuir-type and BET-type isotherms are obtained for adsorption of Triton X-100 and Triton X-305 from water and cyclohexane respectively. Both the contact angles of water for graphite/water/air and graphite/water/cyclohexane decrease monotonously with increasing surfactant concentration. From these results, it is proposed that the adsorption of Triton X-100 and Triton X-305 on carbon black or graphite from water is monolayer. For the adsorption from cyclohexane solutions, the ethyleneoxide group of the surfactant molecules may be adsorbed onto the polar spot at the surface of carbon black, and the hydrophobic group of adsorbed molecules may direct toward the liquid phase or attaches to the nonpolar surface region around the polar spot. As the concentration increases, the ethylene oxide groups of the adsorbed molecules can be aggregated with each other via polar interactions to form hemi-reversed micelle.     

聚乙二醇、聚丙二醇和环氧乙烷-环氧丙烷嵌段共聚物在固-液界面上的吸附 III:硅烷化活性炭/水和甲基化硅胶/水界面

测定了25℃时硅烷化不同时间(1至30天)的活性炭及甲基化硅胶自水溶液中吸附四种聚乙二醇(PEG)、三种聚丙二醇(PPG)和环氧乙烷(EO)-环氧丙烷(PO)嵌段共聚物pluronic-L64的等温线。结果表明, 在各活性炭样品上的等温线均为Langmuir型的; 同一炭样对不同PEG的极限吸附量(g·g^-^1)与分子量无关; 极限吸附时每个PEG分子所占面积(A)与分子中所含EO数(nEO)间有直线关系, 直线的斜率与硅烷化时间有关, 这一结果可用硅烷化时间延长时吸附分子的EO基可能以其氧原子向水, 碳氢链节靠近固体表面取向的模型解释。根据PPG的极限吸附量与分子量有关和极限吸附时的分子面积推断PPG分子不是以平躺方式吸附。甲基化硅胶对PEG的吸附量极小, 对PPG的吸附量随分子量减小急剧降低, 而对L64的吸附量明显大于在亲水硅胶上的。文中对所得结果给出了初步的解释。     

杂多酸的固载化研究(II)

研究了以多种方法化学改性的不同活性炭表面化学特性及十二硅钨酸（SiW_(12)）在相应表面的吸附. 首次提出，不同原料来源和改性的活性炭对SiW_(12)的吸附有不同的等温线形式和吸附力. 活性炭表面的羰基有利于SiW_(12)的吸附，而表面的羧基则是不利的．     

XPS study of carboxylic acid layers on oxidized metals with reference to particulate materials

Low‐molecular‐weight organic additives such as stearic acid are commonly used as surface additives in powder injection moulding (PIM). It is therefore important to know how the additives interact with the surface of the powder used. In this study, such interactions are studied by means of controlled adsorption of carboxylic acids on the oxides of interest. The oxides are prepared by oxidation of flat samples of Fe, Cr, Mn and Si. Surface chemical characterization is done by means of XPS, the main approach on flat samples being a comparison of angle‐resolved analysis and the use of the Tougaard nanostructure analysis technique. Taking advantage of this comparison, the Tougaard method is then applied in the evaluation of XPS analyses of stainless‐steel powder with adsorbed stearic acid. In addition, time‐of‐flight SIMS analysis is used to verify the adsorption of stearic acid on the powder surface. It is shown that Tougaard nanostructure analysis can be used for determining the thickness of an organic layer on particulate material. The layer thickness of adsorbed stearic acid was estimated to be ～20 Å, corresponding to monolayer adsorption. Time‐of‐flight SIMS analysis verified the adsorption of stearic acid on the powder surface. From the XPS analysis of flat samples it was determined that the use of the metal/oxide universal cross‐section in Tougaard nanostructure analysis best described the increased background due to adsorption of carboxylic acids, and that information about molecular orientation could be gained. Copyright © 2003 John Wiley & Sons, Ltd.     

Sorption of ethanesulfonic acid by nylon-6 containing various numbers of end groups

From the analysis of the permeation of ³⁵S labeled ethanesulfonic acid, through nylon-6 films sorption isotherms were obtained. The films are characterized by their largely different content of carboxyl and amino end groups. It was found that the shape of the isotherm depends on the molar ratio of the two end groups: an S-shape curve for the film containing the carboxyl end group larger than the amino end group and a Langmuir-type curve for the film containing comparable numbers of end groups. These results were explained by the McGregor-Harris theory in which the acid dissociation constants of the two end groups in nylon were estimated experimentally.     

Studies of the adsorption of oligomers and surfactants on carbon and steel surfaces in a hydrocarbon medium

The adsorption isotherms for an (amino) terminally functionalised, oligomeric polyisobutylene and for a series of alkylpropoxylate or alkylbutoxylate surfactant molecules on carbon particles, in isooctane, have been obtained. The isotherms on carbon show that the oligomer is the most strongly adsorbing species. The surfactants show some evidence of forming aggregates on the carbon surface at higher concentrations. Analysis of the adsorption isotherms indicate that the size of these aggregates is similar on the carbon particles and on steel balls, reported previously, but that in some cases the actual adsorbed amounts on the two surfaces differ considerably. Ellipsometric studies carried out in situ on steel surfaces in isooctane show that only the polymer gives a relatively thick adsorbed layer. Addition of surfactant reduces the adsorption of the oligomer. There are some differences between the thickness values reported previously using AFM, compared to those found in the current work using ellipsometry, but in both cases it would seem that some degree of multilayer adsorption is occurring for the oligomer on steel in isooctane.     

Reaction scheme of ammonia synthesis in the ECR plasmas

The reaction scheme of ammonia synthesis in the ECR plasma apparatus teas investigated from both identifications of the species in the plasmas and the adsorbed species on the surface of a steel substrate placed in the plasmas. The adsorbed species were considerably different when different kinds of plasmas are used. NH, species were adsorbed on the steel substrate surface in the nitrogen-hydrogen plasma, and N₂ molecules were adsorbed in the nitrogen plasma. By the application of a negative bias potential on the substrate, the adsorption of N atom or Fe-N bond formation was identified on the steel substrate surface. When the stainless steel wall of the chamber was covered with aluminum foil, the yield of NH,, radicals, which were on both the substrate and in the plasma, decreased. By exposure of the substrate, on which N₂ molecules or N atoms adsorbed, to the hydrogen plasma, N₂ and N disappeared from the steel substrate surface, forming ammonia. Moreover, the adsorption of NH,, radicals disappeared when the stainless steel wall surface was covered with aluminum foil. Thus, the surface of the stainless steel wall acts as a catalyst in ammonia formation. The formation of ammonia in the nitrogen-hydrogen ECR plasma, in which the steel substrate served as the catalyst, is not only through the dissociative adsorption of excited nitrogen molecules but also through the dissociative adsorption of nitrogen molecular ions.     

Quantum-Chemical Investigation of the Interaction of Water and Methanol Molecules with Surface Carboxyl Groups on Graphite

A quantum-chemical investigation made of the adsorption of water and methanol at hydrophilic centers (carboxyl groups) on the partly oxidized surface of graphite was undertaken. The enthalpy of adsorption of water and methanol at such centers was determined. It was shown that water is adsorbed at the surface carboxyl groups in the form of dimers, while methanol is adsorbed in the form of single molecules. It was confirmed that the formation of clusters of water molecules in the vicinity of the hydrophilic center is a characteristic feature of the adsorption of water on the surface of graphite and other adsorbents.     

Adsorption Activity and Molecular Dynamics Study on Anti-corrosion Mechanism of Q235 Steel

The correlation between inhibition efficiency and molecular structures of the inhibitor during hydrochloric acid corrosion of Q235 steel was studied by quantum chemical calculations and molecular dynamics(MD) simulation. The proton affinity(PA) calculations demonstrated that 2-(quinolin-2-yl)quinazolin-4(3H)-one inhibitor has the tendency to be protonated in hydrochloric acid, which was in good agreement with experimental observations. Besides, quantum chemical parameters revealed that the protonated corrosion inhibitor molecules were more easily adsorbed on Q235 steel surface and improved the corrosion resistance of steel. MD simulations were implemented to search for the adsorption behavior of this molecule on Fe (110) surface, which might be used as a convenient tool for estimating the interaction mechanism between inhibitor and iron surface.     

Adsorption of Pesticides on Soil Components

The adsorption of two pesticides (2,4-phenoxy acetic acid (2,4D) and thiabendazol) on silica, alumina, kaolin and montmorillonite is studied from adsorption isotherms and enthalpies. 2,4D is not adsorbed by silica, kaolinite and montmorillonite even in the presence of 0.01 mol l?1 divalent cations. On alumina, the energy of adsorption is comparable with that of the formation of an acid-base complex. Thiabendazol can be adsorbed on silica and clays from an ethanol solution. Most adsorption isotherms are of the Langmuir type and correspond to roughly constant adsorption enthalpies as a function of coverage except for kaolin where adsorption on both lateral and basal faces can be involved. Adsorption after introducing humic acids to the system was also studied for kaolin.     

Modeling the adsorption of citric acid onto Muloorina illite and related clay minerals

The adsorption of citric acid onto goethite, kaolinite, and illite was measured as a function of pH (adsorption edges) and concentration (adsorption isotherms) at 25 degrees C. The greatest adsorption was onto goethite and the least onto illite. Adsorption onto goethite was at a maximum below pH 5 and decreased as the pH was increased to pH 9. For kaolinite, maximum adsorption occurred between pH 4.5 and pH 7, decreasing below and above this pH region, while for illite maximum adsorption occurred between about pH 5 and pH 7, decreasing at both lower and higher pH. ATR-FTIR spectra of citrate adsorbed to goethite at pH 4.6, pH 7.0, and pH 8.8 were compared with those of citrate solutions between pH 3.5 and pH 9.1. While the spectra of adsorbed citrate resembled those of the fully deprotonated solution species, there were significant differences. In particular the C[bond]O symmetric stretching band of the adsorbed species at pH 4.6 and 7.0 changed shape and was shifted to higher wave number. Further spectral analysis suggested that citrate adsorbed as an inner-sphere complex at pH 4.6 and pH 7.0 with coordination to the surface most probably via one or more carboxyl groups. At pH 8.8 the intensity of the adsorbed bands was much smaller but their shape was similar to those from the deprotonated citrate solution species, suggesting outer-sphere adsorption. Insufficient citric acid adsorbed onto illite or kaolinite to provide spectroscopic information about the mode of adsorption onto these minerals. Data from adsorption experiments, and from potentiometric titrations of suspensions of the minerals in the presence of citric acid, were fitted by extended constant-capacitance surface complexation models. On the goethite surface a monodentate inner-sphere complex dominated adsorption below pH 7.9, with a bidentate outer-sphere complex required at higher pH values. On kaolinite, citric acid adsorption was modeled with a bidentate outer-sphere complex at low pH and a monodentate outer-sphere complex at higher pH. There is evidence of dissolution of kaolinite in the presence of citric acid. For illite two bidentate outer-sphere complexes provided a good fit to all data.     

Adsorption of organic matter at mineral/water interfaces. IV. Adsorption of humic substances at boehmite/water interfaces and impact on boehmite dissolution

The adsorption of Suwannee River fulvic acid (SRFA) and Pahokee peat humic acid (PPHA) at the boehmite (gamma-AlOOH)/water interface and the impact of SRFA on boehmite dissolution have been examined over a wide range of solution pH conditions (pH 2-12), SRFA surface coverages (Gamma(SRFA), total SRFA binding site concentration normalized by the boehmite surface area) of 0.0-5.33 micromol m(-2), and PPHA surface coverages (Gamma(PPHA), PPHA binding site concentration normalized by boehmite surface area) of 0.0-4.0 micromol m(-2), using macroscopic adsorption and in situ attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. At relatively high SRFA surface coverages (Gamma(SRFA) = 5.33 micromol m(-2)), in situ ATR-FTIR spectral features of adsorbed SRFA are very similar to those measured for SRFA in solution at approximately 1-3 pH units higher. At sub-monolayer surface coverages (Gamma(SRFA) = 1.20 and 2.20 micromol m(-2)), several new peaks and enhancements of the intensities of a number of existing peaks are observed. The latter spectral changes arise from several nonorganic extrinsic species (i.e., adsorbed carbonate and water, for alkaline solution conditions), partially protonated SRFA carboxyl functional groups (near-neutral pH conditions), and small quantities of inner-spherically adsorbed SRFA carboxyl groups and/or Al(III)-SRFA complexes (for acidic conditions). The spectra of PPHA adsorbed at boehmite/water interfaces also showed changes generally consistent with our observations for SRFA sorbed on boehmite. These observations confirm that SRFA and PPHA are predominantly adsorbed at the boehmite/water interface in an outer-sphere fashion, with minor inner-sphere adsorption complexes being formed only under quite acidic conditions. They also suggest that the positively charged boehmite/water interface stabilizes SRFA and PPHA carboxyl functional groups against protonation at lower pH. Measurements of the concentration of dissolved Al(III) ions in the absence and presence of SRFA showed that the boehmite dissolution process is clearly inhibited by the adsorption of SRFA, which is consistent with previous observations that outer-spherically adsorbed organic anions inhibit Al-(oxyhydr)oxide dissolution.     

Inhibition by sodium citrate on 67Ga adsorption to various materials

The adsorption of 67Ga to the inner surface of stainless steel, polyethylene and silicone tubings was studied. The three tubings remarkably adsorbed 67Ga in order of stainless steel, silicone and polyethylene tubing. Sodium citrate inhibited the adsorption of 67Ga in a dose-dependent manner. These phenomena were also observed in blood sampling via the catheter inserted into the external jugular vein. These results show that constant concentration of sodium citrate is necessary for the in vitro study of 67Ga in order to prevent the adsorption to the surface of experimental materials.     

Wettability of calcite and mica modified by different long-chain fatty acids (C18 acids)

The effect of long-chain fatty acid adsorption on the wetting states of calcite and mica powders is investigated. The selected long-chain fatty acids are saturated or unsaturated aliphatic acids (stearic acid and oleic acid, respectively) and naphthenic acids with saturated or unsaturated aromatic rings (18-cyclohexyloctadecanoic acid and 18-phenoloctadecanoic acid, respectively). The amount of irreversibly adsorbed acid is determined by thermogravimetric analysis. The affinity of water and n-decane for these samples before and after modification is deduced from their adsorption isotherm and microcalorimetry. Thermodynamic analysis of surface pressure and spreading tension are performed based on adsorption isotherms. The enthalpy versus coverage curve for water adsorption and its comparison to liquefaction enthalpy is shown to be a meaningful method for characterizing the wettability of a surface. The naphthenic acid with unsaturated aromatic ring deeply modifies the calcite to an oil-wet state. The mica powder was not as strongly modified as calcite by these acid molecules.