紫外/臭氧法PDMS表面亲水改性机理研究

紫外/臭氧改性法是一种操作简单、成本低廉的PDMS表面亲水改性方法。采用该方法对PDMS表面进行亲水改性,利用接触角测量仪对改性效果进行评价,并与PDMS无臭氧紫外法进行了比较。测试表明PDMS表面经紫外/臭氧法处理12小时后,表面接触角达到60°左右,在空气中放置两周后仍保持较好的亲水性。其改性机理可以通过多种表征手段进行分析。红外光谱测试可以看出,PDMS在经过紫外/臭氧改性后,其表面官能团变化明显,随改性时间延长,疏水基团—CH₃逐渐减少,亲水基团Si—OH和—OH逐步增加,二氧化硅典型红外光谱峰也同时出现。通过扫描电镜和能谱测试可以看出,PDMS表面经过改性产生了二氧化硅为主的硅的氧化物。综合上述结果,紫外/臭氧处理法能够使PDMS表面亲水基团增多,同时生成类玻璃态SiO_x薄层,既改善了PDMS表面的亲水性,又阻止了PDMS表面疏水性的完全恢复,亲水性可以长时间保持。     

Patterning and modification of PDMS surface through laser micromachining of silicon masters and molding

We describe preparation of micro patterned PDMS sample surfaces and their chemical modification for the purposes of increased hydrophobicity. The process includes ablation of micrometer sized patterns on a silicon master by pulsed radiation from a Nd:YAG laser, transfer of the patterns to PDMS through molding, and chemical modification of the topmost surface layers of the polymer sample by further laser irradiation and UV/ozone treatment. The samples were characterized by XPS, FTIR, contact angle measurements, optical microscopy and SEM. The study shows the feasibility of the method to manufacture regular patterns with micron-sized cylindrical pillars and to control surface composition. In the absence of chemical modification of the surfaces due to preparation, we compare the effect of increased roughness on the contact angle with theoretically predicted values. Samples with patterned and chemically modified surfaces due to UV/ozone treatment show reduced hydrophobicity. PACS 52.38.Mf; 81.65.Cf; 81.05.Lg     

Use of thermal imaging to characterize laser light reflection from thermoplastics as a function of thickness,laser incidence angle and surface roughness

Laser light reflection during the laser transmission welding (LTW) of thermoplastics has the potential to overheat and/or cause unintentional welding of adjacent features of the part being welded. For this reason, and in order to assess how much light is being absorbed by the transparent part (after measurement of the light transmitted through the transparent part), it is important to be able to quantify the magnitude and distribution of reflected light. The magnitude and distribution of the reflected light depends on the total laser input power as well as its distribution, the laser incidence angle (angle between the normal to the transparent part surface and the laser beam), the laser light polarization as well as the surface and optical properties of the transparent part. A novel technique based on thermal imaging of the reflected light was previously developed by the authors. It is used in this study to characterize the magnitude and distribution of reflected light from thermoplastics as a function of thickness (1–3.1 mm), laser incidence angle (20–40°) and surface roughness (0.04–1.04 μm). Results from reflection tests on nearly polished nylon 6 (surface roughness between 0.04 and 0.05 μm) have shown that, for the various thicknesses tested (1–3.1 mm), the total reflection was larger than the specular top surface reflection predicted via the Fresnel relation. From these observations, it is conjectured that, in addition to top surface reflection, the bulk and/or bottom surface also contribute to the total reflection. The results also showed that reflection decreased slightly with increasing thickness. As expected, for the p-polarized light used in this study, the reflection decreased with increasing angle of incidence for the range of angles studied. It was also found that when the surface roughness was close to zero and when it was close to the wavelength of the input laser beam (i.e. 940 nm), the reflectance values were close and reached a minimum between these two roughness values.     

Posterior capsular opacification and intraocular lens surface micro-roughness characteristics: an atomic force microscopy study

ObjectiveSurface roughness parameters of various intraocular lenses (IOLs) biomaterials using atomic force microscopy (AFM) are compared. Variation, if any, in the micro-roughness properties of different IOLs made up of the same biomaterial is also explored. Retrospective analysis of posterior capsular opacification (PCO) incidence has been followed up for a period of four years post IOL implantation to evaluate the correlation of PCO formation with surface roughness of IOLs.DesignExperimental materials study.Materials and participantsSurface characteristics of 20 different IOL models were assessed using AFM. These IOL models were made up of PMMA or HEMA or acrylic hydrophobic or acrylic hydrophilic or silicone. Retrospective analysis of PCO incidence in 3629 eyes of 2656 patients implanted with the same IOL models was performed.MethodsTopological characteristics of 20 different IOLs made up of 5 different biomaterials including (i) PMMA, (ii) HEMA, (iii) acrylic hydrophobic, (iv) acrylic hydrophilic and (v) silicone were evaluated using AFM in the tapping mode. Images were acquired with a resolution of 256 × 256 data points per scan at a scan rate of 0.5 Hz per line and a scan size of 10 × 10 μm. Rate of PCO formation in 3629 eyes of 2656 patients implanted with the five different IOL biomaterials was retrospectively analyzed.ResultsAFM images of IOL optic surfaces showed a collection of pores, grooves, ridges and surface irregularities. Surface roughness parameters of the IOL optics were significantly different on comparing lenses of different materials. Acrylic hydrophobic IOLs had minimum surface roughness while acrylic hydrophilic IOLs showed the highest surface roughness. Different IOL models of the same biomaterial showed varied topological roughness characteristics. Retrospective analyses of PCO formation rate after IOL implantation was carried out, which revealed that rate of PCO incidence, was directly proportional to the increase in surface micro-roughness of IOLs.ConclusionsAFM is a powerful technique for the topological characterization of IOLs. Acrylic hydrophobic IOLs showed minimum surface roughness properties as well as minimum PCO incidence over a period of four years post implantation. It is, therefore, tempting to consider acrylic hydrophobic IOLs over other IOL biomaterials as the ideal biocompatible material for lowering PCO incidence. These results suggest an urgent need for manufacturers to optimize the various steps involved in the fabrication of IOLs.     

Substrate bias effects during diamond like carbon film deposition by microwave ECR plasma CVD

Diamond like carbon (DLC) coatings were deposited on silicon(1 1 1) substrates by microwave electron cyclotron resonance (ECR) plasma CVD process using a plasma of Ar and CH₄ gases under the influence of DC self bias generated on the substrates by application of RF (13.56 MHz) power. DLC coatings were deposited under the varying influence of DC bias (−60 V to −150 V) on the Si substrates. Deposited films were analyzed by different techniques like: X-ray photoelectron spectroscopy (XPS), spectroscopic ellipsometry (SE), atomic force microscopy (AFM), Hardness and elastic modulus determination technique, Raman spectroscopy, scanning electron microscopy (SEM) and contact angle measurement. The results indicate that the film grown at −100 V bias has optimised properties like high sp³/sp² ratio of carbon bonding, high refractive index (2.26–2.17) over wide spectral range 400–1200 nm, low roughness of 0.8 nm, high contact angle (80°) compared to the films deposited at other bias voltages (−60 V and −150 V). The results are consistent with each other and find august explanation under the subplantation model for DLC growth.     

Rapid surface roughness measurements of silicone thin films with different thicknesses

A rapid optical measurement system for rapid surface roughness measurement of polycrystalline silicon (poly-Si) thin films was developed in this study. Two kinds of thickness of poly-Si thin films were used to study rapid surface roughness measurements. Six different incident angles were employed for measuring the surface roughness of poly-Si thin films. The results reveal that the incident angle of 20° was found to be a good candidate for measuring the surface roughness of poly-Si thin films. Surface roughness (y) of poly-Si thin films can be determined rapidly from the average value of reflected peak power density (x) measured by the optical system developed using the trend equation of y = ?0.1876x + 1.4067. The maximum measurement error rate of the optical measurement system developed was less than 8.61%. The savings in measurement time of the surface roughness of poly-Si thin films was up to 83%.     

Determination of solid material elastic modulus and surface energy based on JKR contact model

The JKR contact theory is employed to study the adhesion phenomena between two solid materials in intimate contact. The elastic contact modulus and the work of adhesion of solid materials are obtained during adhesion tests by utilizing a micro force-deflection measuring apparatus. Six of the plastic materials, including polyethylene polyoxymethlene (POM), polyamide (PA), terephthalate (PET), polyvinyl chloride (PVC), polypropylene (PP), and ultra-high molecular weight polyethylene (UHMWPE) are used to evaluate the adhesion effect implied by the JKR theory. Comparison is made between surface energy obtained from the adhesion tests with that by a dynamic contact angle analyser.Results show that the load/deflection data in the loading phase are in good agreement with the predictions of JKR equation, and the experimental data of unloading phase deviate significantly from the JKR theory. The phenomena of adhesion hysteresis in loading tests are responsible for these results due to the effects of molecular reconstruction on solid surfaces in contact. The work of adhesions, and hence surface energies of plastic materials, calculated by the best fitting of JKR equation with the experimental data in the loading phase, agree satisfactorily in a comparable manner with that obtained using the contact angle analyser.     

PDMS改性环氧树脂/Sm2O3复合涂层的近红外光谱及疏水性研究

以聚二甲基硅氧烷（PDMS）改性环氧树脂（HYSZ）为粘合剂,Sm₂O₃为功能颜料,纳米SiO₂为微纳结构改性剂,制备得到了一种同时具有良好疏水性能和附着力的近红外吸收涂层。系统分析了PDMS和HYSZ质量比、邻苯二甲酸二辛酯(DOP)添加量、总填料添加量、Sm₂O₃和纳米SiO₂质量比对涂层性能的影响。结果表明：PDMS改性可明显降低涂层的表面能,从而使涂层的疏水性得到明显增强。利用DOP强化涂层韧性和微观搭桥作用可增强涂层整体性,从而可明显提高涂层的附着力和近红外吸收性能。涂层的表面粗糙度可随总填料添加量的增加而明显升高,进而可使涂层表现出更优的疏水性能。当涂层中PDMS和HYSZ质量比、DOP添加量、总填料添加量、Sm₂O₃和纳米SiO₂质量比分别为1∶9,20%,50%和5.5∶4.5时,涂层同时具有良好的近红外低反射率（59.1%）、疏水性能（水接触角为137°）及附着力（2级）。     

Surface topography,nano-mechanics and secondary structure of wheat gluten pretreated by alternate dual-frequency ultrasound and the correlation to enzymolysis

The effects of alternate dual-frequency ultrasound (ADFU) pretreatment on the degree of hydrolysis (DH) of wheat gluten (WG) and angiotensin I-converting enzyme (ACE) inhibitory activity were investigated in this research. The surface topography, nano-mechanics and secondary structure of WG were also determined using atomic force microscope (AFM) and circular dichroism (CD). The correlations of ACE inhibitory activity and DH with surface topography, nano-mechanics and secondary structure of WG were determined using Pearson’s correlation analysis. The results showed that with an increase in either pretreatment duration or power, the ACE inhibitory activity of the hydrolysate also increases, reaching maximum at 10 min and 150 W/L, respectively, and then decreases thereafter. Similarly, AFM analysis showed that as the pretreatment duration or power increases, the surface roughness also increase and again a decrease occurs thereafter. As the pretreatment duration or power increased, the Young’s modulus and adhesion of WG also increased and then declined. Young’s modulus and adhesions average values were compared with ACE inhibitory activity reversely. The result of the CD spectra analysis exhibited losses in the relative percentage of α-helix of WG. Pearson’s correlation analysis showed that the average values of Young’s modulus and the relative percentage of α-helix correlated with ACE inhibitory activity of the hydrolysates linearly and significantly (P < 0.05); the relative percentage of β-sheet correlated linearly with DH of WG significantly (P < 0.05). In conclusion, ADFU pretreatment is an efficient method in proteolysis due to its physical and chemical effect on the Young’s modulus, α-helix and β-sheet of WG.     

Wettability,optical property of a superhydrophobic YAG film

A flame-like superhydrophobic yttrium aluminum garnet surface was obtained by a simple approach under ambient conditions. The influences of the concentration of curing agent and paraffin wax in course of the experiment were investigated. The as-prepared film shows superhydrophobicity which has a water contact angle of 158 ± 1.0°, and sliding angle of 4 ± 1.0°. Moreover, the water contact angle of the rough surface remained higher than 150°, after exposure for 10 days. Transmission electronic microscope, scanning electronic microscope, fluorescence spectrometer and atomic force microscope were also used to characterize the samples.     

Rapid optical measurement of surface texturing result of crystalline silicon wafers for high efficiency solar cells application

Surface texturing of crystalline silicon (c-Si wafers) wafers is a frequently used technique in high efficiency solar cells processing to reduce the light reflectance. Measuring the surface texturing result is important in the manufacturing process of high efficiency solar cells because the surface texturing of c-Si wafers is sensitive to the performance of reducing front reflection. Traditional approach for measuring surface roughness of texturing of c-Si wafers is atomic force microscopy. The disadvantage of this approach include long lead-time and slow measurement speed. To solve this problem, an optical inspection system for rapid measuring the surface roughness of texturing of c-Si wafers is proposed in this study. It is found that the incident angle of 60° is a good candidate for measuring surface roughness of texturing of c-Si wafers and y = ?188.62x + 70.987 is a trend equation for predicting the surface roughness of texturing of c-Si wafers. Roughness average (Ra) of texturing of c-Si wafers (y) can be directly determined from the peak power density (x) using the optical inspection system developed. The results were verified by atomic force microscopy. The measurement error of the optical inspection system developed is approximately 0.89%. The saving in inspection time of the surface roughness of texturing of c-Si wafers is up to 87.5%.     

Laser welding of structural steels: Influence of the edge roughness level

Laser welding continues to become more extensively used in many industrial applications and in the last 10 years an increasing number of studies have examined ways to increase the efficiency of the process. This study investigates the influence of joint edge surface roughness on weld quality and penetration depth. The characteristics are investigated of welded samples of two low alloyed steels, S355 and St 3, of 20 mm thickness with various joint edge surface roughness levels in butt joint configuration. Welding was performed with different fiber lasers with a wavelength of 1070 nm at power levels from 10 to 15 kW. The absorption characteristics were evaluated at 10 kW power level using a calorimeter. There was a significant positive correlation between edge surface roughness level and the penetration depth. Optimum roughness levels to provide maximum penetration depth are presented. The highest penetration depth at power levels of 14 and 10 kW was achieved at R_a=6.3 μm.     

Treatment of PVC using an alternative low energy ion bombardment procedure

In many applications, polymers have progressively substituted traditional materials such as ceramics, glasses, and metals. Nevertheless, the use of polymeric materials is still limited by their surface properties. Frequently, selective modifications are necessary to suit the surface to a given application. Amongst the most common treatments, plasma immersion ion implantation (PIII) has attracted the attention of many researchers owing to its versatility and practicality. This method, however, requires a power supply to provide high voltage (tens of kV) negative pulses, with a controlled duty cycle, width and frequency. Owing to this, the implementation of PIII on the industrial scale can become economically inviable. In this work, an alternative plasma treatment that enables low energy ion bombardment without the need of a high voltage pulse generator is presented. To evaluate the efficiency of the treatment of polymers, polyvinylchloride, PVC, specimens were exposed to 5 Pa argon plasmas for 3600 s, at excitation powers, P, of between 10 and 125 W. Through contact angle and atomic force microscopy data, the influence of P on the wettability, surface free energy and roughness of the samples was studied. Surface chemical composition was measured by X-ray photoelectron spectroscopy, XPS. To evaluate the effect of aging under atmospheric conditions, contact angle and XPS measurements were performed one and 1334 days after the treatment. The plasma potential and ion density around the driven electrode were determined from Langmuir probe measurements while the self-bias potential was derived with the aid of an oscilloscope. From these data it was possible to estimate the mean energy of ions bombarding the PVC surface. Chlorine, carbon and oxygen contamination were detected on the surface of the as-received PVC. Upon exposure to the plasma, the proportion of chlorine was observed to decrease while that of oxygen increased. Consequently, the wettability and surface energy increased after the treatment but such modifications were not stable after aging: the contact angle increased for all the samples, modifying the initially hydrophilic surface into a highly hydrophobic one. Consistently, the surface composition also changed after aging: there was carbon enrichment due to further losses of oxygen and chlorine. Another relevant factor for the elevation of θ was the change in morphology induced by the treatment. At greater powers, the uniform matrix of the PVC was transformed into a columnar structure containing randomly distributed sharp pillars. Interpretation of such results is proposed in terms of the total energy deposited in the solid by ionic collisions.     

Effects of surface mechanical attrition treatment (SMAT) on a rough surface of AISI 316L stainless steel

Surface mechanical attrition treatment (SMAT) improves mechanical properties of metallic materials through the formation of nanocrystallites at their surface layer. It also modifies the morphology and roughness of the work surface. Surface roughening by the SMAT has been reported previously in a smooth specimen, however in this study the starting point was a rough surface and a smoothening phenomenon is observed. In this paper, the mechanisms involved in the surface smoothening of AISI 316L stainless steel during the SMAT are elucidated. The SMAT was conducted on a specimen with a roughness of R_a = 3.98 μm for 0–20 min. The size of milling balls used in the SMAT was varied from 3.18 mm to 6.35 mm. The modification of subsurface microhardness, surface morphology, roughness and mass reduction of the specimen due to the SMAT were studied. The result shows the increasing microhardness of the surface and subsurface of the steel due to the SMAT. The impacts of milling balls deform the surface and produce a flat-like structure at this layer. Surface roughness decreases until its saturation is achieved in the SMAT. The mass reduction of the specimens is also detected and may indicate material removal or surface erosion by the SMAT. The size of milling ball is found to be the important feature determining the pattern of roughness evolution and material removal during the SMAT. From this study, two principal mechanisms in the evolution of surface morphology and roughness during the SMAT are proposed, i.e. indentation and surface erosion by the multiple impacts of milling balls. A comparative study with the results of the previous experiment indicates that the initial surface roughness has no influence in the work hardening by the SMAT but it does slightly on the saturated roughness value obtained by this treatment.     

Nanoscale aggregation phenomena at the contact line of air-drying pure water droplets on silicon revealed by atomic force microscopy

In the present work, silicon wafer surfaces were studied during a pure water dewetting process in ambient conditions by intermittent-contact atomic force microscopy (AFM). With an acid-free surface cleaning, large network structures of tens of microns in extension but only a few nanometers in height were observed, being stable for days. Fractal-like assemblies have been previously reported in a variety of different scenarios, for example, when an aqueous solution of carbon-based species, especially carbon nanotubes, is left to evaporate on a solid substrate, provided that no complete wetting was produced. Chemical mapping of silicon wafer surfaces, while unable to provide a spatial resolution comparable to that of the AFM, clearly showed the initially formed contact line to be enriched in carbon. Therefore, hydrophobic and/or non-soluble (or slightly soluble) substances which are present on every surface exposed to air are expected to be responsible for the observed fractal structures. Reactions of the network structures toward changing environmental conditions were analyzed. When increasing the ambient humidity, the structures grew only slightly, which is indicative of their highly (but not totally) hydrophobic nature. Heating the sample above 100 °C for about 10 h led to an almost complete disappearance of these nanostructures. Due to the lateral extension of these stable network heterogeneities, they are expected to affect contact angle measurements in wetting studies, especially at the micro- and nanoscale. When acid-cleaned wafers are used as substrate, deposited water extends as a film over the silicon surface without droplet formation. No fractal structures are then observed.     

Intensified depolymerization of aqueous polyacrylamide solution using combined processes based on hydrodynamic cavitation,ozone, ultraviolet light and hydrogen peroxide

The present work deals with intensification of depolymerization of polyacrylamide (PAM) solution using hydrodynamic cavitation (HC) reactors based on a combination with hydrogen peroxide (H₂O₂), ozone (O₃) and ultraviolet (UV) irradiation. Effect of inlet pressure in hydrodynamic cavitation reactor and power dissipation in the case of UV irradiation on the extent of viscosity reduction has been investigated. The combined approaches such as HC + UV, HC + O₃, HC + H₂O₂, UV + H₂O₂ and UV + O₃ have been subsequently investigated and found to be more efficient as compared to individual approaches. For the approach based on HC + UV + H₂O₂, the extent of viscosity reduction under the optimized conditions of HC (3 bar inlet pressure) + UV (8 W power) + H₂O₂ (0.2% loading) was 97.27% in 180 min whereas individual operations of HC (3 bar inlet pressure) and UV (8 W power) resulted in about 35.38% and 40.83% intrinsic viscosity reduction in 180 min respectively. In the case of HC (3 bar inlet pressure) + UV (8 W power) + ozone (400 mg/h flow rate) approach, the extent of viscosity reduction was 89.06% whereas individual processes of only ozone (400 mg/h flow rate), ozone (400 mg/h flow rate) + HC (3 bar inlet pressure) and ozone (400 mg/h flow rate) + UV (8 W power) resulted in lower extent of viscosity reduction as 50.34%, 60.65% and 75.31% respectively. The chemical structure of the treated PAM by all approaches was also characterized using FTIR (Fourier transform infrared) spectra and it was established that no significant chemical structure changes were obtained during the treatment. Overall, it can be said that the combination of HC + UV + H₂O₂ is an efficient approach for the depolymerization of PAM solution.     

Optical and morphological properties of N-doped TiO2 thin films

Nitrogen doped titanium dioxide (TiO₂) thin films were deposited by RF magnetron sputtering onto various substrates. The films were prepared in plasma of argon, oxygen, and nitrogen, with varying the nitrogen content, from 0% up to 70%. The resulting TiOx–Ny films were found to consist of cubic TiN osbornite and tetragonal TiO₂ rutile phases. Using optical spectroscopy with large spectral range from 350 to 1000 nm, the band gap width was determined and a narrowing of the optical gap from 2.76 to 2.32 eV was observed as a function of the N-content. It was found that the optical properties of the TiOx–Ny layers are influenced by the surface morphology, roughness, surface energy and phase content. The chemical composition, the crystalline structure, the surface morphology and the surface energy were thoroughly studied by the Rutherford backscattering spectrometry (RBS), grazing-angle XRD, atomic force microscopy (AFM) and contact angle measurements (wettability), respectively.     

Effects of ultrasonic agitation and surfactant additive on surface roughness of Si (1 1 1) crystal plane in alkaline KOH solution

In the silicon wet etching process, the “pseudo-mask” formed by the hydrogen bubbles generated during the etching process is the reason causing high surface roughness and poor surface quality. Based upon the ultrasonic mechanical effect and wettability enhanced by isopropyl alcohol (IPA), ultrasonic agitation and IPA were used to improve surface quality of Si (1 1 1) crystal plane during silicon wet etching process. The surface roughness R_q is smaller than 15 nm when using ultrasonic agitation and R_q is smaller than 7 nm when using IPA. When the range of IPA concentration (mass fraction, wt%) is 5–20%, the ultrasonic frequency is 100 kHz and the ultrasound intensity is 30–50 W/L, the surface roughness R_q is smaller than 2 nm when combining ultrasonic agitation and IPA. The surface roughness R_q is equal to 1 nm when the mass fraction of IPA, ultrasound intensity and the ultrasonic frequency is 20%, 50 W and 100 kHz respectively. The experimental results indicated that the combination of ultrasonic agitation and IPA could obtain a lower surface roughness of Si (1 1 1) crystal plane in silicon wet etching process.     

The fabrication of aspherical microlenses using focused ion-beam techniques

Aspheric lenses are the most common method for correcting for spherical aberrations but, in microlens production, highly-controlled lens profiles are hard to achieve. We demonstrate a technique for creating bespoke, highly-accurate aspheric or spherical profile silicon microlens moulds, of almost any footprint, using focused ion-beam milling. Along with this, we present a method of removing induced ion-beam damage in silicon, via a hydrofluoric acid etch, helping to recover the surface's optical and chemical properties.In this paper, we demonstrate that our milled and etched moulds have a roughness of 4.0–4.1 nm, meaning they scatter less than 1% of light, down to wavelengths of 51 nm, showing that the moulds are suitable to make lenses that are able to handle light from UV up to infra-red.Using empirical experiments and computer simulations, we show that increasing the ion-dose when milling increases the amount of gallium a hydrofluoric acid etch can remove, by increasing the degree of amorphisation within the surface. For doses above 3000 μC/cm² this restores previous surface properties, reducing adhesion to the mould, allowing for a cleaner release and enabling higher quality lenses to be made.Our technique is used to make aspheric microlenses of down to 3 μm in size, but with a potential to make lenses smaller than 1 μm.     

Effects of multi-frequency ultrasound pretreatment under low power density on the enzymolysis and the structure characterization of defatted wheat germ protein

The effects of ultrasonic frequency mode, power density, pretreatment time and other parameters under low power density on the degree of hydrolysis (DH) of defatted wheat germ protein (DWGP) and angiotensin-I-converting enzyme (ACE) inhibitory activity of DWGP hydrolysate were studied in this research. Ultraviolet–visible (UV–Vis) spectra, free sulfhydryl (SH), disulfide bond (SS), surface hydrophobicity and hydrophobic protein content of ultrasound-pretreated protein and hydrophobic amino acid (HAA) content of alcalase-hydrolysate of DWGP were measured under optimized ultrasonic condition. The ultrasonic frequency mode with dual-fixed frequency combination of 28/40 kHz showed higher ACE inhibitory activity of DWGP hydrolysate compared with that of other ultrasound frequency modes and all the ultrasonic frequency combinations involving in 28 kHz showed higher ACE inhibitory activity. Under the dual-fixed frequency ultrasound mode of 28/40 kHz, ultrasonic power density of 60 W/L, pretreatment time of 70 min, temperature of 60°C and substrate concentration of 60 g/L, the ACE inhibitory activity of DWGP hydrolysate was the highest with its value of 74.75% (increased by 62.30% compared to control). However, all the ultrasonic pretreatment did not increase the DH of DWGP significantly (p > 0.05). The changes in UV–Vis spectra, SH and SS groups, surface hydrophobicity and hydrophobic protein content indicated that the structure of DWGP unfolded after ultrasound pretreatment. The HAA content of hydrolysate from the pretreated DWGP increased significantly (p < 0.05). The results proved that ultrasound pretreatment loosed the protein structure and exposed more HAA residues of protein to be attacked easily by alcalase. This resulted in the increase in the HAA content which related to the ACE inhibitory activity.