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The purpose of this paper is to study methods of reacting the surface of the particles of silica sols with silanes, primarily gamma‐glycidoxypropyltrimethoxysilane (GPTMS) and study some basic properties of the modified sols and the nature and structure of the silane groups attached to the particle surface.

The surface of the silica particles was modified by reacting the silica sols with aqueous solutions of silanes, chiefly GPTMS. The presence and structure of silane groups on the particle surface were established by Si‐NMR and C‐NMR, respectively.

Several silanes were studied but silica sols could be readily modified only with GPTMS and glycidoxypropylmethoxydiethoxysilane (GPMDES), most readily if the silanes were pre‐hydrolysed in water. Higher degrees of silylation were preferably done by continuous addition of silane. Lower degrees of modification can be achieved at room temperature by the stepwise addition of the silane solution. The silylation of the silica surface with GPTMS significantly reduces the number of charged surface groups and silanol groups. GPTMS binds covalently to the silica surface and the epoxy ring opens and transforms into a diol. Silica sols modified with GPTMS and GPMDES are stable toward aggregation.

Only organo‐reactive silanes were studied.

This is the first work to study the modification by silanes of silica aquasols with high concentrations of silica. The silane modification can extend the use of silica to areas of applications previously inaccessible to silica sols.

Immersion is one of the key steps during the preparation of silane-based hybrid films, which has important effects on the performance of films after curing. In this paper, the formation process of Zr-doped silane film (i.e. the adsorption of silane and deposition of zirconium compounds) on carbon steel immersed in Zr(NO₃)₄/silane mixed solutions was investigated.

The method of in situ monitoring the open circuit potential of a two-electrode system, consisting of carbon steel and saturated calomel electrode, was used. The effects of immersion conditions (i.e. the concentration of Zr(NO₃)₄ and pH of Zr(NO₃)₄/silane mixed solution) on the open circuit potential were investigated in detail. Furthermore, the surface coverage rate of different cured films (i.e. Zr cured film, silane cured film and Zr/silane composite cured film) after curing on carbon steel was calculated according to the results of polarization curves. Electrochemical impedance spectroscopy (EIS) was used to study the self-healing property of Zr-doped silane cured film.

The results indicate that in Zr(NO₃)₄/silane mixed solutions, most zirconium compounds deposit on the surface of carbon steel at the initial immersing stage, then the adsorption of silane on the residual surface of carbon steel dominates the following immersing stage. EIS results show that the Zr-doped cured film has improved self-healing property.

First, the method of in situ monitoring the open-circuit potential of two-electrode system was applied to investigate the deposition of Zr and the adsorption of silane on carbon steel immersed in Zr(NO₃)₄/silane mixed solutions. Second, the formation process of Zr-doped silane film was proposed.

This study aims to systematically compare the effect of increasing fiber–matrix interface adhesion and matrix toughness in layered composite materials.

Silane ((3-glycidyloxypropyl) trimethoxysilane) was applied to strengthen the fiber–matrix interface connection in e-glass/epoxy laminated composite material. Using a cationic surfactant, 0.1% multi-walled carbon nanotubes (CNTs) were added to the matrix in two different ways, by with and without chemical functionalization using the vacuum infusion method.

In the results obtained from the three-point bending test specimens, it was determined that the synergistic effect of silane application and non-functionalized CNT in the matrix was higher in terms of flexural modulus and strength values.

The functionalization of multi-walled CNT did not give the expected results because of reasons such as viscosity increase and agglomeration in the matrix.

In this study, a simple model for normalization and prediction purposes was developed, which allows the determination of the flexural modulus and un-notched flexural strength values from one test result of the notched specimen. A systematic comparison was performed by varying each parameter in the composite material.

In the preceding three parts of this series, the authors have extensively reviewed and quantified the special processing sequences required for the ‘additive’ and ‘semi‐additive’ process strategies of PWB manufacture. In this, the fourth part of the series of five, they wish to present a series of full build processes which meet all the interconnect requirements of the 1990s while eliminating the drawbacks traditionally associated with additive processes.

The purpose of this paper is to investigate the effect of different PHS on the surface chemistry of fumed silica treated with aminopropyltrimethoxysilane (APTMS).

The reaction conditions involved variation of pH ranging from acidic to alkaline. Different analytical techniques including FT‐IR spectroscopy, thermogravimetric analysis (TGA), CHN and Zeta potential analyses were employed to investigate the surface chemistry of treated particles. In addition, the stability of silanised silica dispersions were studied using turbidimetric and rheometric measurements.

It was revealed that in all conditions silica was more or less chemically grafted by the silane. When the pH of treating bath was adjusted to 1‐2 prior and during the reaction, 58 percent grafting was observed, as obtained by CHN and TGA analyses. At very alkaline conditions, however, the grafting content declined to 29 percent. The variations in grafting were dependent on the silane hydrolysis and its further condensation with the silica surface. Zeta potential measurements showed a drastic change from −7.1 mv to +18.01 mv (at pH 7) for the untreated particle and the one with the highest grafting, respectively. The dispersion stability of differently treated particles varied in solvents with different Hansen solubility parameters (HSP). Moreover, due to the variations of surface chemistry of particles, their rheological behaviours were significantly influenced.

The results obtained in this work showed that the surface chemistry of fume silica could be tuned with treating method. The highest content of grafting led to a better dispersion in solvents having greater hydrogen bonding component and to an inferior dispersion in solvents with higher polar component.

In the industrial silylation process, the cost of production can be greatly reduced by reducing the frequency of the replacement of the silane solution. The purpose of this paper is to describe how a method of discontinuous addition of concentrated solution into the KH560 treatment bath was developed, to improve further the effective availability of the silane solution and reduce cost of production.

The preparation and addition of each incremental amount of concentrated KH560 was studied in detail.

The results indicate that adding concentrated silane solution is an effective method of maintaining the target bath concentration.

The paper describes how a method of adding concentrated KH560 was developed to prolong the working time of KH560 solution for silane coating production, and to improve the availability of the KH560 in solution. The results indicated that adding concentrated solution was an effective method of prolonging the working time of the silane solution. The mixture ratio of the concentrated solution, and the volume of each incremental amount, both affected the performance of the KH560 solution.

The purpose of this paper was to prepare a hybrid organic/inorganic coating with interesting barrier properties against the corrosion of plain carbon steel sheets in 3.5 per cent NaCl solution. The search for replacing chromates in protective coatings has led to the development of hybrid sol-gel anticorrosive coatings. Appropriate functionalization can dramatically enhance the chemical durability and mechanical strength of these coatings.

To prepare the targeted coating, 1,2-epoxybutane (EB) was mixed with 2 to 4 per cent aminoethylaminopropyl-methylsiloxane dimethylsiloxane (APDMS) copolymer and 1,6-diaminohexane. The above coating (EBAC) has been further mixed with three different corrosion inhibitors “Moly-white® 101-ED, Heucophos Zapp® and cerium ammonium nitrate”, yielding the coatings EBAC-M, EBAC-Z and EBAC-Ce, respectively. The corrosion characteristics of all coatings on the steel panels immersed in 3.5 per cent NaCl solution were obtained using different electrochemical methods such as electrochemical impedance spectroscopic and Tafel polarization measurements.

The newly prepared coatings showed interesting protection properties for protecting the steel substrate against corrosion in chloride-containing media.

The results provide a good approach for the modification of polydimethylsiloxane coatings using a simple organic modifier.

The purpose of this work was to prepare a hybrid organic/inorganic coating with interesting barrier properties against the corrosion of plain carbon steel sheets in 3.5 per cent NaCl solution. The search for replacing chromates in protective coatings has led to the development of hybrid sol-gel anticorrosive coatings. Appropriate functionalization can dramatically enhance the chemical durability and mechanical strength of these coatings.

To prepare the targeted coating, 1,2-epoxybutane (EB) was mixed with 2-4 per cent aminoethylaminopropyl-methylsiloxane dimethylsiloxane copolymer and 1,6-diaminohexane. The above coating (EBAC) was further mixed with three different corrosion inhibitors “Moly-white® 101-ED, Hfucophos Zapp®” and Cerium Ammonium Nitrate, yielding the coatings (EBAC-M), (EBAC-Z) and (EABC-Ce), respectively. The corrosion characteristics of all coatings on carbon steel panels immersed in 3.5 per cent NaCl solution were obtained using different electrochemical methods such as electrochemical impedance spectroscopic and Tafel polarization measurements.

The newly prepared coatings showed interesting properties for protecting the steel substrate against corrosion in chloride containing media.

The results provide a good approach for the modification of polydimethylsiloxane coatings using a simple organic modifier.

Silane cross-linkers have been used to strengthen the mechanical stabilities and friction resistance of plastic products. Therefore, the effect of silane cross-linkers on latex has been studied through preparing modified self-cross-linking long fluorocarbon polyacrylate latex. In this paper, nonionic surfactant alcohol ether glycoside (AEG1000) and anionic polymerizable surfactant 1-allyloxy-3-(4-nonylphenol)-2-propanol polyoxyethylene (10) ether ammonium sulfate (DNS-86) acted as mixed emulsifier and 3-(methacryloyloxy) propyltrimethoxysilane (KH-570) and bis (2-ethylhexyl) maleate (DOM) were used as functional monomers.

The modified acrylate polymer latex was synthesized through the semi-continuous seeded emulsion polymerization with methyl methacrylate (MMA), butyl acrylate (BA), dodecafluoroheptyl methacrylate (DFMA) and hydroxypropyl methacrylate (HPMA) as main monomers. Potassium persulfate (KPS) was applied to initiate polymerization reaction, nonionic surfactant AEG1000 and DNS-86 acted as emulsifier, KH-570 and DOM were used as functional monomers, respectively.

The optimum conditions of synthesizing the modified latex were the following. The mass ratio of monomers containing MMA, BA, DFMA, HPMA, KH-570 and DOM was 13.58:13.58:0.90:1.20:0.15:0.60, the usage of initiator KPS was 0.5% of the total weight of monomers and the amount of emulsifier was 7% of all monomers with AEG1000:DNS-86 = 1:1. The results indicated that the conversion of monomer was 99% and the coagulation was about 2.0%.

The resultant latex was modified silane cross-linker KH-570 and DOM, which positively affected the comprehensive properties of latex and its film. Apart from this, the novel mixed emulsifier was used to improve the size and distribution of latex particles and reduce environmental problems caused by the use of emulsifiers.