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1.
The effect of ionic strength ( I) on the interfacial interactions between pectin and the bovine serum albumin (BSA) surface has been investigated using the quartz crystal microbalance with dissipation monitoring (QCM-D). As I increases from 0.01 to 0.02 M, the frequency shift (Delta F) decreases, whereas the energy dissipation shift (Delta D) changes toward a higher value. Further increase of I from 0.02 to 0.5 M causes both Delta F and Delta D to gradually return to almost zero. The adsorbed mass and thickness of the pectin adlayer estimated from the Voigt model confirm that the adsorption of pectin and the formation of thicker pectin adlayers on a BSA surface are favored by the increase of ionic strength at I = 0.01 approximately 0.02 M. An increase of I above 0.02 M hinders pectin adsorption and causes the formation of a thinner pectin adlayer. The ionic strength-enhanced effect at I values lower than 0.02 M is explained as an increase of ionic strength that can screen the electrostatic repulsion to a larger extent than the electrostatic attraction between pectin and BSA. However, when I is higher than 0.02 M, both electrostatic repulsion and attraction can be significantly screened by the increasing ionic strength, resulting in the ionic strength-reduced effect. On the other hand, the high viscoelasticity of the pectin adlayer revealed by the Voigt model suggests the formation of a network-structured pectin adlayer on the BSA surface, which contains two steps for higher pectin adsorptions at I = 0.0125 approximately 0.1 M by the indication of two slopes in Delta D-Delta F plots.  相似文献   

2.
Quartz crystal microbalance with dissipation monitoring (QCM-D) has been employed to study the interactions between (-)-epigallocatechin gallate (EGCG) and bovine serum albumin (BSA) surface. The adsorbed mass, thickness, and viscoelastic properties of EGCG adlayer on BSA surface at various EGCG concentrations, temperatures, sodium chloride concentrations, and pH values have been determined by QCM-D in combination with the Voigt model. The adsorption isotherm of EGCG on BSA surfaces can be better described by the Freundlich model than the Langmuir model, indicating that EGCG adsorption on BSA surfaces is dominated by nonspecific hydrophobic interactions, as supported by stronger EGCG adsorption at higher temperature. Shifts in the Fourier transform infrared spectra of the BSA surface with and without EGCG adsorption disclose that hydrogen bonding might also be involved in EGCG adsorption on BSA surfaces. The addition of salt and change of pH can also influence the EGCG adsorption on BSA surfaces. Usually, higher EGCG adsorption leads to higher values of viscosity and shear elastic modulus of EGCG adlayer, which can be explained by the aggregation of BSA through EGCG bridges. Compared with EGCG, nongalloylated (+)-catechin shows much lower adsorption capacity on BSA surfaces, suggesting the importance of the galloyl group in polyphenol/protein interactions.  相似文献   

3.
Interfacial protein-polysaccharide complexes can be used to improve the physical stability of oil-in-water emulsions. The purpose of this study was to examine the impact of ionic strength on the formation and stability of oil-in-water emulsions containing polysaccharide-protein-coated droplets. Emulsions were prepared that contained 0.1 wt % corn oil, 0.05 wt % beta-lactoglobulin, and 0.02 wt % pectin at pH 7. The emulsions were then adjusted to pH 4 to promote electrostatic deposition of the pectin molecules onto the surfaces of the protein-coated droplets. The salt concentration of the aqueous phase (0 or 50 mM NaCl) was adjusted either before or after deposition of the pectin molecules onto the droplet surfaces. We found that stable emulsions containing polysaccharide-protein-coated droplets could be formed when the salt was added after pectin adsorption but not when it was added before pectin adsorption. This phenomenon was attributed to the ability of NaCl to promote droplet flocculation in the protein-coated droplets so that the pectin molecules adsorbed onto the surfaces of flocs rather than individual droplets when salt was added before pectin adsorption. We also found that polysaccharide-protein-coated droplets had a much improved stability to salt-induced flocculation than protein-coated droplets with the same droplet charge (zeta-potential). Theoretical predictions indicated that this was due to the ability of the adsorbed polysaccharide layer to strongly diminish the van der Waals attraction between the droplets.  相似文献   

4.
The adsorption of an anionic surfactant sodium dodecyl sulfate (SDS) on a negatively charged silica was studied to provide a better understanding of surfactant adsorption phenomena in an electrostatic repulsion environment between surfactant and soil. The adsorption experiment was conducted under different electrolyte concentration and pH. Results indicated that adsorption happened with hydrophobic interaction, although electrostatic repulsion was generated between SDS and silica surface. The adsorption amount decreased with decreasing electrolyte concentration and increasing pH due to the increase of electrostatic repulsion. The influence of electric potential near the silica surface on the adsorption was confirmed with the modified Langmuir adsorption equation, 1-pK basic Stern model and zeta potential. Because silica is ubiquitous in soils and the water environment, the adsorption characteristics of an anionic surfactant is important when we consider the fate of an anionic surfactant in the environment. The result is also useful when considering the fate of agricultural chemicals which contain negative charge and hydrophobic sites.  相似文献   

5.

Purpose

Despite experiments with humic substances and positively charged proteins, the colloidal behavior of HS-protein mixture in the system of two immiscible liquids has been neglected. In this context, the main objective of this study was to reveal the interference of HS and globular proteins on its partition in an aqueous/organic liquid system and the adsorption at liquid/liquid interface as a model of natural organic matter interaction with proteins in nature at hydrophobic/hydrophilic surfaces.

Materials and methods

Coal humic acids (HA) and two globular proteins lysozyme and albumin were under the test. Aqueous phase was prepared in phosphate-buffered saline (pH 7.2?±?0.1, 0.16 M); p-xylene was chosen as an organic phase. Experiments were performed for fixed concentration of protein (0.1 g L?1 for lysozyme and 0.06 g L?1 for albumin) and varied HA concentration from 0.2 to 50 mg L?1. Radiotracer method including tritium thermal activation and scintillation phase method, dynamic light scattering, and optical microscopy were used to control mixed adsorption layer at the aqueous/p-xylene interface and composition of each contact phase.

Results and discussion

The results suggest that if both HA and protein are negatively charged (HA-albumin mixture), the mechanism of interaction between them in the bulk of water and at liquid/liquid interface is controlled by HA concentration. At low HA concentrations, free protein prevents HA adsorption at liquid/liquid interface and its transition to the organic phase via coulomb repulsion. At high HA concentration, the formation of hydrophilic complexes occurs via both electrostatic attraction between positively charged amino acid residues and the hydrophobic interaction. In HA-lysozyme mixture, the interaction between protein and HA is preferably provided by electrostatic attraction that provides higher hydrophobicity of HA-lysozyme complex compared with free HA. An increase in HA concentration results in partial recharge of the conjugate that leads to lysozyme amount reduction at the interface. We also measured the composition of spontaneously formed precipitate of HA-lysozyme conjugate and followed its self-organization.

Conclusions

This work demonstrates colloidal chemical behavior of net positively and negatively charged model protein by coal humic acids under environmentally relevant solution conditions in the system of two immiscible liquids that were used as a model of natural membrane. For the first time, quantities of both protein and HA in mixed adsorption layer at the liquid/liquid interface in the cases of positively and negatively charged protein have been determined.  相似文献   

6.
The pH of samples of a soil was altered by mixing them either with acid or lime, and incubating the moistened samples at 60°C for a day. The sorption of selenate and of selenite was then measured using as background electrolytes, 0.01 M, 0.1 M and 1.0 M sodium chloride and also 0.01 M calcium chloride. The results were compared with previous studies with phosphate and fluoride. Selenite was sorbed more strongly than selenate, but not as strongly as phosphate or fluoride. Sorption of both selenite and selenate decreased with increasing pH. This decrease was more marked for selenate than for selenite; more marked in a sodium system than in a calcium one; and more marked with a dilute background electrolyte than a concentrated one. Under certain conditions, the steeper curves for the dilute electrolyte crossed the curves for the concentrated electrolyte giving points of zero salt effect. For selenite, these points of zero salt effect occurred near pH 6 and the greater the sorption the lower the pH for zero salt effect. For phosphate, the analogous value was near pH 5. For selenate, if a point of zero salt effect occurred, it was at such a high pH and such a low amount of sorption that it could not be measured. Thus, the larger the amount of sorption the lower the pH for the point of zero salt effect. This generalization applied both within and between different kinds of sorbates. The results were closely described by a model that had previously been applied to phosphate and fluoride. The model postulates that ions react with charged surfaces. The electric potentials of the reacting surfaces are affected by the identity and concentration of the background electrolyte and this produces the interactions between pH and electrolyte concentration. The model also postulates that there is a distribution of electric potentials. Anions react with surfaces which occur in the more positive tail of this distribution. The smaller the amount of the reaction the more positive the potential of the reacted surface and, therefore, the higher the pH required to decrease this potential to zero.  相似文献   

7.
The constraint imposed by phosphate (PO4) deficiency on soil fertility in Botswana necessitated the study of ionic strength (μ) and pH effects on electric charge distribution and PO4 adsorption of two representative soils: Typic Pellustert and Typic Haplustalf. Electric charge increased with increasing soil pH, but the effect of µ on electric charge distribution was indistinct. The point-of-zero-salt-effect (PZSE) occurred at pH 4.8 in the Pellustert and at almost 6.0 in the Haplustalf. Ionic strength decreased PO4 adsorption in the Pellustert, but increased it in the Haplustalf. The Scatchard and reciprocal linearization of the Langmuir model adequately described PO4 adsorption of the soils under varying µ and pH × µ conditions. The PO4 adsorption maxima (M) and affinity index (b) decreased with increasing µ in the Pellustert, but not in the Haplustalf. The decreasing M and b with increasing µ in the Pellustert was explained by electrostatic repulsion from the highly negative charge surface, whereas the increasing M and b with increasing µ in the Haplustalf was attributed to enhanced access to the surface sorption sites due to compression of diffuse double layer. Under varying pH × µ conditions, PO4 sorption sites were resolved into low- and high-energy sites, depending on the concentration of added PO4. Because b is related to the ease of PO4 detachment from soil surfaces into solution for plant uptake or leaching, PO4 added to this Pellustert at µ > 0.01 would likely leach freely, and hence µ monitoring is imperative for PO4 fertilization strategy of this Pellustert.  相似文献   

8.
The influence of globular protein denaturation after adsorption to the surface of hydrocarbon droplets on flocculation in oil-in-water emulsions was examined. n-Hexadecane oil-in-water emulsions (pH 7.0) stabilized by beta-lactoglobulin (1-wt % beta-Lg) were prepared by high-pressure valve homogenization. NaCl (0-150 mM) was added to these emulsions immediately after homogenization, and the evolution of the mean particle diameter (d) and particle size distribution (PSD) was measured by laser diffraction during storage at 30 degrees C for 48 h. No change in d or PSD was observed in the absence of added salt, which indicated that these emulsions were stable to flocculation. When 150 mM NaCl was added to emulsions immediately after homogenization, d increased rapidly during the following few hours until it reached a plateau value, while the PSD changed from monomodal to bimodal. Addition of N-ethylmaleimide, a sulfhydryl blocking agent, to the emulsions immediately after homogenization prevented (at 20 mM NaCl) or appreciably retarded (at 150 mM NaCl) droplet flocculation. These data suggests that protein unfolding occurred at the droplet interface, which increased the hydrophobic attraction and disulfide bond formation between droplets. In the absence of added salt, the electrostatic repulsion between droplets was sufficient to prevent flocculation, but in the presence of sufficient salt, the attractive interactions dominated, and flocculation occurred.  相似文献   

9.
钟凯  徐仁扣  赵安珍  姜军  李航 《土壤》2011,43(2):312-316
选择海南岛北部3个不同年代喷发的玄武岩发育的土壤研究了其对铬酸根(CrO42-)和磷酸根(PO43-)的吸附特征,结果表明随着母岩年龄的增加,土壤发育程度提高,土壤游离氧化铁和表面正电荷数量增加,对2种阴离子的吸附量增加。土壤CrO42-的解吸率在19.8%~39.6%之间,表明土壤对CrO42-的吸附涉及静电吸附和专性吸附2种机制,且随着土壤发育程度增加,CrO42-静电吸附所占比例增加。土壤对PO43-的吸附以非静电吸附为主,吸附的PO43-的解吸量非常低,其解吸率不超过6%。吸附PO43-在去离子水中的解吸量高于在0.1 mol/L NaNO3和KNO3中的解析量,KNO3体系中的解吸量低于NaNO3体系中的,电解质主要通过改变胶体表面离子吸附面上的静电电位影响PO43-的解吸。  相似文献   

10.
Adsorption of Potassium and Calcium Ions by Variable Charge Soils   总被引：1，自引：1，他引：1  
Interactions of potassium and calcium ions with four typical variable charge soils in South China were examined by measuring pK-0.5pCa value with a potassium ion-selective electrode and a calcium ion-selective electrode,and pK value with a potassium ion-selective electrode.The results showed that adsorption of potassium and calcium ions increased with soil suspension pH,and the tendency of the pK-0.5pCa value changing with pH differed with respect to pH range and potassium to calcium ratio.Adsorption of equal amount of calcium and potassium ions led to release of an identical number of protons,suggesting similar adsorption characteristics of these two ions when adsorbed by variable charge soils.Compared with red soil,latosol and lateritic red soil had higher adsorption selectivities for calcium ion.The red soil had a greater affinity for potassium ion than that for calcium ion at low concentration,which seems to result from its possession of 2:1 type minerals,such as vermiculite and mica with a high affinity for potassium ion.The results indicated that adsorption of potassium and calcium ions by the variable charge soils was chiefly caused by the electrostatic attraction between the cations and the soil surfaces.Moreover,it was found that sulfate could affect the adsorption by changing soil surface properties and by forming ion-pair.  相似文献   

11.
The pH of samples of a soil was altered by adding acid or lime and incubating the moistened soil at 60°C. The effect of varying the concentration of salt on pH, retention of phosphate, and retention of zinc was then measured. At low pH, increasing the concentration of salt decreased phosphate retention; at high pH, it increased it. The pH at which the effects crossed over (that is, the point of zero salt effect on phosphate retention) was higher than the point of zero salt effect on pH. This is opposite to effects observed with uniform surfaces. These results were described by a model in which it was assumed that individual sites varied in their electrostatic potential and that phosphate was retained preferentially by sites with the highest potential. Zinc retention was decreased by high concentrations of salt. This was partly because of effects of salt in decreasing the pH of solutions in contact with soil. There was no indication of a crossing-over of effects at low pH. This suggested that the electrostatic potential of zinc-retaining sites did not vary much with pH.  相似文献   

12.
The adsorption of Cd, Cu, Pb, and Zn from 0.025 M NaClO4 solutions by two ferruginous subsoils, Christiana silty clay loam and Dothan sandy clay, was investigated. Under acidic conditions, selective dissolution and removal of the Fe oxide soil component by dithionite-citrate-bicarbonate (DCB) generally increased heavy metal adsorption by the soils. This effect was attributed to increased electrostatic attraction of cations to the DCB-washed soils as evidenced by substantial reduction in the zero point of charge (ZPC) for the Dothan soil following DCB extraction. Alternately, the DCB extraction stripped Fe and Al species bound to structural exchange sites or eliminated coatings which reduce cation accessibility to such sites. Addition of low levels (10?6 M) of ferric iron suppressed heavy metal adsorption capacity of the DCB-extracted Christiana soil to values comparable to the unmodified whole soil system. While hydrous oxide surfaces represent highly reactive sites for cation binding, Fe oxides can modify both the pH-dependent and structural exchange sites in a manner which hinders heavy metal adsorption. Thus, a soil's Fe-oxide content is unlikely to be a reliable guide to heavy metal adsorption capacity.  相似文献   

13.
可变电荷土壤中特殊化学现象及其微观机制的研究进展   总被引：3，自引：0，他引：3  
徐仁扣  李九玉  姜军 《土壤学报》2014,51(2):207-215
综述了近年来可变电荷土壤化学研究的进展,着重总结了可变电荷土壤中的盐吸附、铁铝氧化物对土壤自然酸化的抑制作用和离子强度对离子专性吸附的影响等特殊化学现象及其微观机制的研究进展。用颗粒表面扩散层重叠导致有效电荷数量减小的原理解释了盐吸附现象和铁铝氧化物对土壤自然酸化的抑制作用。阐明了可变电荷土壤和矿物中介质离子强度影响离子专性吸附的机制,用四层吸附模型解释了离子专性吸附随离子强度增大而增加的现象,并根据胶体zeta电位随离子强度改变而变化的趋势进一步证明了离子强度增大使胶体专性吸附面上静电电位的绝对值减小,是离子专性吸附随离子强度增大而增加的主要原因。带电颗粒表面双电层结构和双电层相互作用的深入研究,有助于阐明可变电荷土壤中一些特殊化学现象的微观机理,从而进一步完善土壤化学理论。  相似文献   

14.
The adsorption of orthophosphate to humic surfaces was studied in a model experiment. The adsorption maximum of humic substances greatly increased with higher concentrations of organically complexed Fe (III), indicating that orthophosphate was bound to humic surfaces via metal bridges. The molar ratio Padsorbed/Fe was nearly 1 for Fe freshly complexed to humic substances, whereas the ratio for amorphous Fe-oxide was a tenfold lower. An increase in pH from 5.2 to 6.2 lead to an increase of P-adsorption of about 30% in the case of humic-Fe-surfaces, which could be explained by an increased accessibility of adsorption sites at pH 6.2. The addition of a 0.01 M CaCl2-matrix increased orthophosphate adsorption at pH 6.2 but not at pH 5.2. This could be explained by electrostatic interactions caused by the Ca++ ion.  相似文献   

15.
Experiments on the adsorption of alpha-zein (characterized by SDS-PAGE) from aqueous ethanol and 2-propanol solutions onto hydrophilic and hydrophobic surfaces are reported. Zein adsorption onto self-assembled monolayers (SAMs) was detected by surface plasmon resonance (SPR). Gold substrates were prepared by thermal evaporation on glass slides. Gold-coated surfaces were modified by depositing SAMs of either a long-chain carboxylic acid terminated thiol [COOH(CH2)(10)SH] or a methyl-terminated alkanethiol [CH3(CH2)(7)SH]. Experimental measurements indicated that zein interacted with both hydrophilic and hydrophobic surfaces. Zein concentration affected the thickness of bound zein layers. The estimated thickness of the zein monolayer deposited on hydrophilic surfaces was 4.7 nm. Zein monolayer thickness on hydrophobic surfaces was estimated at 4.6 nm. The topography of zein layers was examined by atomic force microscopy (AFM) after solvent was evaporated. Surface features of zein deposits depended on the adsorbing surface. On hydrophilic surfaces, roughness values were high and distinct ring-shaped structures were observed. On hydrophobic surfaces, zein formed a uniform and featureless coverage.  相似文献   

16.
The potential competitive effect of background electrolytes (Na2HPO4 ·2H2O, NaHCO3, Na2SO4 and NaCl solutions) on arsenate adsorption onto synthetic 2-line ferrihydrite has been studied by means of kinetic batch experiments conducted at pH values from 4.0 to 10.0 and at anionic concentrations of 0.01 and 0.1 M. The results indicate that the adsorptive capacity of ferrihydrite for arsenate decreases strongly in the presence of phosphate species at pH in the range of 4–10 and in the presence of bicarbonate at pH 8.3 as a consequence of their competitive effect. Analogously to phosphate, a surface interaction of inner-sphere type between ferrihydrite and bicarbonate is suggested. Chloride has negligible effects on arsenate adsorption processes, confirming it as an outer-sphere ion that does not compete with the inner-sphere binding peculiar to arsenate onto ferrihydrite. Sulphate exhibits an intermediate behaviour; at 0.01 M concentration, the competitive effect of sulphate is similar to that of chloride, whereas at 0.1 M concentration sulphate shows a moderate influence on arsenate adsorption. The results of the kinetic studies can be summarised by the following order of competitive capacity: phosphate?>?carbonate?>?sulphate?>?chloride. The process of arsenate adsorption follows pseudo-second order kinetics and the reaction half-time notably increases in the presence of strong competitor anions such as phosphate and carbonate with respect to an ineffective competitor anion such as chloride. Modelling of arsenate adsorption with PHREEQC, according to the Generalized Two-Layer Model, confirms that the pH effect is notably less important than the competitive effect of carbonate species in determining the amount of arsenate adsorbed onto ferrihydrite at pH 8.3 in 0.1 M NaHCO3 solution, whereas the model greatly underestimates the competitive effect of carbonate species at pH 8.3 in 0.01 M NaHCO3 solution. The results of the batch experiments in 0.1 M NaHCO3 solution are substantiated by XPS analyses of ferrihydrite after immersion in the same solution, both with and without dissolved arsenate. XPS confirms the interaction between ferrihydrite surface and arsenate; the binding energy of As3d shifts towards higher binding energies after adsorption with respect to the pure compound Na2HAsO4·7H2O taken as reference standard. In presence of carbonate species, the As3d binding energy is found at intermediate values. XPS quantitative analysis shows a depletion of arsenate on ferrihydrite surface, providing further evidence of the competition of the two species (i.e. arsenate and bicarbonate) for the ferrihydrite adsorption sites. Important environmental implications concerning arsenic mobility, as well as possible application in various fields (e.g. irrigation agriculture, soil decontamination, water treatment), might derive from these findings.  相似文献   

17.
Spherical biochar derived from saccharides (glucose, sucrose, and xylose) was prepared through two steps: pre-hydrothermal carbonization at 190 °C and calcination at low temperatures (200–325 °C). The spherical biochar was characterized by Brunauer–Emmett–Teller (BET) surface area analysis, Fourier transform infrared spectroscopy, zeta potential, scanning and transmission electron microscopies, and X-ray diffraction. The result indicated that the spherical biochar exhibited low S BET (15–22 m2/g), but abundant superficial active oxygen-containing functional groups. The spherical biochar possessed a negatively charged surface within solution pH 2.0–11. The adsorption process of Pb2+, Cu2+, and methylene green 5 (MG5) was strongly dependent on the solution pH and reached fast equilibrium at approximately 60 min. The maximum Langmuir adsorption capacity (Q°max) exhibited the following order: glucose-biochar > sucrose-biochar > xylose-biochar prepared at 300 °C. The selective adsorption order of glucose-biochar was Cu2+ (0.894 mmol/g) > Pb2+ (0.848 mmol/g) > MG5 (0.334 mmol/g). The electrostatic attraction played a determining role in the adsorption mechanism of pollutant cations. The adsorption of anionic dye (acid red 1) on the spherical biochar was negligible because of electrostatic repulsion. The spherical biochar can serve as a newer and promising adsorbent to remove toxic pollutant cations from water media.  相似文献   

18.
Borate sorption by a soil was measured with 0.01, 0.1, or 1.0 M sodium chloride as background electrolyte and samples of soil with a range of pH values achieved by incubating with either calcium carbonate or hydrochloric acid for 24 h at 60°C.
Borate sorption generally increased with increasing pH. The more concentrated the electrolyte, the steeper the increase. At low pH, increasing the salt concentration decreased borate sorption; at high pH, it increased sorption. There was an intermediate pH at which salt had no effect on borate sorption. The point of zero salt effect on borate sorption was at a higher pH than the point of zero salt effect on pH. This result was explained by a mechanism in which borate ions react with variable charge surfaces which are heterogeneous and for which part of the heterogeneity is in the electric potential of the surfaces. It cannot be explained by mechanisms which do not take into account the effects of the electric potential of the reacting surfaces on the reaction with borate ions. Although the behaviour of borate was broadly consistent with that of other anions, it differed in that about half of the heterogeneity had to be allocated to the binding constant for borate ions. It was suggested that this was because reaction with organic matter was more important for borate than for other anions.  相似文献   

19.
Abstract

The “Four-plane model” is one of the surface complexation models developed for analyzing the electrostatic charge of synthetic oxides. This model which was applied to the B horizon of Andisols, was equilibrated with an electrolyte solution containing KCl, KNO3, K2SO4 in the concentration range of 0.0033, 0.01, 0.033, 0.1 M, and pH range of 2 to 11. The amounts of NO3 -, Cl-, SO4 2-, and K+ adsorbed were determined from the products remaining in the liquid phase. The increase in the pH value results in the increase of K+ adsorption, and decrease of anion adsorption. The increase in the equilibrium concentration increased both K+ and anion adsorption. The parameters of the model were determined by measurements and the iterative method. The model have a good agreement between calculated and measured values of cation and anion adsorption. Among the anion species, the amount of adsorbed anions was in the order of SO4 2-?Cl->NO3 -. The differences in the degree of adsorption were mainly associated with the differences in the equilibrium constants of surface complexation. The surface complexation of the anions produced a negative charge and increased cation adsorption. The degree of surface complexation was most significant in the K2SO4 solution, and the phenomenon was considered to be important not only for anion adsorption but also for cation adsorption on Andisols.  相似文献   

20.
The adsorption of a commercial zein sample on carboxylic (COOH) and alkyl (CH(3)) surfaces was monitored by high time resolution surface plasmon resonance. Zein showed higher affinity and higher mass adsorption on carboxylic than alkyl surfaces. A zein layer specific for each surface was obtained after flushing off loosely bound zein with 75% 2-propanol solutions. Zein deposits were examined under atomic force microscopy. Differences in layer thickness between carboxylic and alkyl surfaces were explained in terms of zein adsorption footprint.  相似文献   

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