Abstract
Kinetic features of the formation of epoxy nanocomposites with carbon (nanotubes, graphene, and graphite), metal-containing, and aluminosilicate (montmorillonite and halloysite) fillers are considered. In contrast to linear polymers, epoxy nanocomposites are obtained only via the curing of epoxy oligomers in the presence of filler or the corresponding precursor. These additives may affect the kinetics of the process and the properties of the resulting matrix. A high reactivity of epoxy groups and a thermodynamic miscibility of epoxy oligomers with many substances make it possible to use diverse curing agents and to accomplish curing reactions under various technological conditions. The mutual effect of both a matrix and nanoparticles on the kinetics of the composite formation is discussed.
Keywords
- polymer nanocomposites
- epoxy matrices
- nanoparticles
- synthesis of composites
- epoxy oligomers
1. Introduction
Since around the mid-1990s, polymer nanocomposites have become the subject of considerable attention, as evidenced by monographs, and a great number of reviews [1]. The application of nanocomposites is associated with their unique properties related to a huge specific surface and high surface energy of nanoparticles. Nanosized particles, as opposed to microinclusions and coarser inclusions, are not stress concentrators, and this circumstance facilitates a marked improvement in the mechanical properties of nanocomposites. Compared with the respective polymers, the transparency of nanocomposites does not decrease, because nanoparticles do not scatter light because of their small sizes. Depending on the type of nanoparticles introduced in polymeric materials even at a low concentration, nanocomposites acquire remarkable chemical (primarily catalytic), electrophysical, and biomedical properties, thereby opening wide potential for their use [1].
Among polymer nanocomposites, it would appear that composites based on an epoxy matrix occupy an insignificant place—nearly 10% as to the number of publications—but an ever-increasing number of papers appear annually. Moreover, the interest in them grows almost exponentially, as evidenced by the number of citations [2].
Epoxy polymers in terms of a set of properties stand out among other polymeric materials and play an important role in aerospace, automotive, shipbuilding, and other industries. Their wide application in engineering is associated, firstly, with a high processability of epoxy resins and, secondly, with the unique combination of performance characteristics of their curing products [3, 4, 5].
A high reactivity of epoxy groups and a thermodynamic miscibility of epoxy oligomers with many substances make it possible to use diverse curing agents and to accomplish curing reactions under various technological conditions [6, 7, 8]. Of no small importance are the features of synthesis processes, such as the absence of volatile products and low level of shrinkage.
Epoxy polymers have high values of static and shock strength, hardness, and wear resistance. They possess marked thermal stability and heat resistance. Many solid surfaces form strong adhesive bonds with epoxy polymers [2, 3]. This circumstance determines their use as compounds, glues, paint and lacquer materials, and coatings, including in aerospace engineering. Epoxy nanocomposites are designed to realize the unique functional properties of nanoparticles: electric, magnetic, optical, chemical, and biological.
Information about epoxy nanocomposites is contained most completely in [2]. Reviews [9, 10] are devoted to epoxy nanocomposites with carbon nanotubes (CNTs). Some aspects of epoxy nanocomposites containing graphene were covered in [11].
Taking into consideration the urgency of the issue and the presence of recent studies not covered in the mentioned reviews, author took a chance to consider epoxy nanocomposites containing metal and mineral nanoparticles, graphene, and CNTs and to discuss kinetic features of the processes of their formation.
2. Feature of synthesis of epoxy nanocomposites
The generally accepted scheme of the amino-epoxy cure involves two main reactions of the glycidyl ether:
Epoxy-amine cure reactions scheme.
In principle, a reaction of esterification is possible—the resulting hydroxyls with epoxy groups.
The ratio of the rate constant of the secondary amine in addition to the corresponding constant of the primary one depends on electron-donating properties of an amine and may vary with temperature. Normally this ratio varies within 0.1–0.6. It is because of accumulation of hydroxyl groups during the reaction that the process of curing epoxy oligomers under the action of amines has autocatalytic character. Kinetics is often analyzed using empirical Eq. (1):
where α is the degree of conversion of epoxy groups; the sum of exponents
From the standpoint of formation of epoxy nanocomposites, there are two types of fillers: fillers belonging to the first type are chemically unchanged and should be reduced to the desired size in one way or another. An example is provided by CNTs, diverse minerals, and graphene. Compounds whose chemical nature changes during composite formation belong to the second type. These are, in particular, metal salts, in which cations should be reduced to the zero-valence state.
In contrast to linear polymers, epoxy nanocomposites are obtained only via the curing of epoxy oligomers in the presence of filler or the corresponding precursor. It is evident that these additives may affect the kinetics of the process and the properties of the resulting matrix. The mechanism of curing of epoxy resins is fairly complicated, because many reactions occur simultaneously and depend on such phenomena as gelation and glass transition [6, 7]. After incorporation of nanoparticles into the epoxy resin, the process of its curing becomes even more complicated. A considerable number of papers concern the kinetics of curing of epoxy systems with various types of nanoparticles.
Most of kinetic studies are using DSC. DSC analysis has shown that etherification occurs at elevated temperatures once all the primary amines are exhausted. In this case, the data are analyzed as a rule in terms of the generalized formula:
For nonisothermal conditions the temperature varies with time with a constant heating rate, β =
Isoconversional kinetic analysis has shown that the reaction rate at constant conversion depends only on the temperature. In other words,
where
The analysis performed in [12] showed that the calculation can be reconciled with the experiment by specifying the values of
3. Influence of the fillers on the nanocomposite synthesis process
3.1 Carbon fillers: CNTs, graphene, graphite, and carbon fiber
Taking into consideration the molecular structure of carbon nanoparticles, in particular, graphene and CNTs [13, 14, 15, 16, 17], it may be stated that their influence on the kinetics of the process of curing of epoxy oligomers will be similar. Indeed, graphene, CNTs, and other compounds with the
In work [25] the high-temperature isothermal curing of tetraglycidyl-4,4′-diamino-diphenylmethane with 4,4′-diaminodiphenyl sulfone (DDS) in the presence of multi-wall CNTs was investigated.
The typical technique used to prepare the reaction mixture for kinetic studies of the process will be described below, and the techniques described in other papers may differ from the typical one only in some details.
A mixture of an epoxy resin with preliminarily purified multi-wall CNTs was sonificated for 2 h and placed in an oil bath at temperature of 120°С, and the stoichiometric amount of a curing agent was slowly added under continuous mechanical stirring until formation of a homogeneous mixture. This process took nearly 10 min.
The kinetics was analyzed using Eq. (1). It was found that with the increase in concentration of CNTs, constant
The initial acceleration of the reaction under the action of single-wall CNTs was also observed [26], but the magnitude of this effect was insignificant. At the same time, the glass-transition temperature
The effect of concentration and type of CNTs (single-, double-, and multi-wall) on the kinetics of reaction between low-viscosity mixture of epoxy oligomers and amine curing agents was studied by Esmizadeh et al. [27]. The analysis was conducted in terms of the equation:
It was shown that the type of CNTs exerts almost no effect on kinetic parameters possibly because of their low concentration (0.01%). At a concentration of 0.1, 0.2, and 0.5%, the rate constant changes nonmonotonically, but on the whole it is lower than that in the absence of CNTs. The energy of activation increases from ∼6 to ∼9 kJ/mol. The heat of reaction decreases, indicating the incompletion of the process. This is also evidenced by a decrease in the high-elasticity modulus, i.e., matrix network density. In accordance with [27], the observed effects may be explained by the increase in the viscosity and thermal conductivity of the system in the presence of CNTs, although these properties were not estimated.
Multi-wall CNTs, when taken at low concentrations (0.5%), slightly accelerate the reaction of amine curing of bisphenol F diglycidyl ether, while at higher concentrations (1.5%) decelerate this reaction as shown by Visco et al. [28]. They believe that the rate of the process is controlled by viscosity of the system.
The curing of an epoxy resin is regarded as a heterogeneous phase formation process, and the role of multi-wall CNTs is discussed from this viewpoint by Susin et al. [29]. They believe that the tubes restrict the local free volume and assist in the development of the heterogeneous morphology in resin, especially at high content of multi-wall CNTs. At the same time, with the increase in their concentration (to 1%), the ultimate heat of reaction increases, while the energy of activation decreases.
Most of kinetic studies are aimed at gaining insight into the effect of functionalized CNTs using DSC. Rahaman and Mohanty [30] presented the data of the influence of multi-wall CNTs carrying СООН groups on the process of curing of epoxy resin EPOLAM with anhydride of 1,2,3,6-tetrahydroxymethyl-1,3,6-methanephthalic acid. According to these authors, this dependence provides evidence that in the presence of multi-wall CNTs, the degree of cross-linking increases; as a result, the mobility of unreacted groups declines. The closeness of the curves at the beginning of the curing process indicates that the addition of CNTs does not affect the value of
Note that methods using the dependence of a change in the exothermal peak on the rate of heating cannot provide reasonable isothermal predictions for the kinetics of curing of epoxy compounds because of the autocatalytic character of the process [6, 7]. The presence of at least two kinetic constants, as in Eq. (1), should be taken into account.
In this context, deserve attention other methods, which, depending on the type of study or the nature of epoxy resins, can be successfully used [31]. Among them, for example, the method of luminescence spectroscopy makes it possible to determine the degree of conversion with high accuracy at the final stage of reaction. This is hardly achievable by other methods. Analysis with the aid of a rheometer provides information about the time of gelation which cannot be obtained by another method.
The DSC studies [32] showed that multi-wall CNT with COOH functionalization act as catalysts, stimulating the initial stage of curing of bisphenol A diglycidyl ether (BADGE). This accelerating effect is noticeable even at a 1% content of multi-wall CNTs. Nonfunctionalized multi-wall CNTs decrease the degree of cross-linking, as evidenced by a lower overall heat of reaction and lower glass-transition temperatures of the nanocomposites compared with the neat epoxy resin. At the same time, the functionalization of multi-wall CNTs increases the degree of cross-linking.
Compared with the neat epoxy resin, 1% of carboxylated multi-wall CNTs decreases the heat of reaction and increases the energy of activation [33]. Fluorinated tubes insignificantly influence the value of
The grafting of butylamine onto plasma- and CF4-treated single-wall CNTs markedly improves the ultimate conversion, whereas clean tubes, when the reaction is accomplished in the nonisothermal regime, have no effect on this parameter, while in the case of the isothermal regime (30°C), they decrease it [34].
There was another conclusion [35] that clean and aminated single-wall CNTs reduce the ultimate heat of reaction. Tubes with the grafted epoxy groups give almost the same value of heat as that obtained in the curing of resin without any filler: 355 versus 362 J/g. It is possible that different results may be attributed to different concentrations of single-wall CNTs.
The kinetic analysis of the curing process in terms of Eq. (1) does not reveal marked differences in the values of constants and exponents for the systems of interest. However, it was shown [36] that the introduction of 3% of clean multi-wall CNTs does not influence the kinetics of reaction, but tubes with grafted amino groups decrease the constant
Multi-wall CNTs with amino groups decelerate the curing of BADGE with 2-ethyl-4-methylimidazole at concentrations of 0.5 and 1 wt % [37], but the deceleration effect vanishes at a concentration of nanoparticles of 3%. However, in this case, the value of ultimate reaction heat decreases as well. Note that clean multi-wall CNTs accelerate curing of the same reaction system [32].
The impact of multi-wall CNTs carrying acidic and amino groups on the process of curing was studied by Raman and luminescence spectroscopy [38]. Throughout the reaction conducted in the presence of nanoparticles, the rates were higher than the neat resin. The difference in the rates of curing was explained by homogeneity of the sample and the presence of chemical groups.
The kinetics of the amine curing of BADGE in the presence of multi-wall CNTs functionalized by oxygen-containing groups using viscometry and transmission electron microscopy along with calorimetry was analyzed [39]. The samples of multi-wall CNTs had different values of specific surface
The kinetic features of the process may become understandable if the micrograph of the epoxy composition which is measured at the initial stage of curing performed in the presence of multi-wall CNTs is examined (Figure 1). It is seen that compact polymer structures grow along the tube. Evidently, hydroxyl groups grafted on the surface catalyze the reaction of epoxy groups with amine [7] to give rise to new hydroxyl groups accelerating this reaction. In doing so, the process of polymer formation is localized, and the reaction assumes the frontal character. The natural consequence of the localization process is the formation of ineffective cross-links. Therefore, the value of critical conversion increases, and correlation is observed between the time of a sharp gain in viscosity and the specific surface of multi-wall CNTs.
It was shown that graphene oxide (GO) accelerates the curing of tetraglycidyl-4,4′-diaminodiphenylmethane with 4,4′-diaminodiphenyl sulfone [40]. According to this work, this effect is related to the presence of hydroxyl and carboxyl groups on the surface of GO.
The kinetics of the nonisothermal curing of BADGE with liquid poly(amido- amine) in the presence of amine-functionalized GO using Eq. (6) was investigated [41]. It is seen that for the systems without any filler and in the presence of GO containing NH2 groups, the parameters of this equation are similar. At the same time, GO slightly decelerates the process.
The mixture of BADGE and 1,1,2,2-tetra(
The IR spectral analysis of the curing of BADGE with 4,4'-diaminodiphenylmethane in the presence of GO permitted to obtain kinetic curves for both epoxy groups and primary, secondary, and tertiary amino groups [44]. These studies made a considerable contribution to gaining insight into the mechanism of reaction. It was shown that the original GO has no effect on the overall kinetics of the process and even decelerates the consumption of primary amino groups. But after autoclave purification, GO increases the rate of reaction of epoxy groups by more than factor of 2 and the rate of reaction of primary amino groups by factor of 1.8. As was shown by X-ray photoelectron spectroscopy, purification leads to a marked reduction in the amount of oxygen-containing groups on the surface of GO. The glass-transition temperature of a nanocomposite based on the crude GO is much lower than that of the epoxy matrix, whereas the purification of GO causes an increase in this parameter, although
The influence of various graphite fillers (graphite with a high surface area, graphite oxide, and exfoliated graphite oxide) on the reaction of epoxy ring opening of BADGE by amines—primary (benzylamine and cyclohexylamine) and secondary (dibenzylamine)—and hydroxyl (benzyl alcohol) was studied [45]. These data indicate the strong catalytic effect of fillers on the reaction with amines. This effect is the most pronounced for the exfoliated graphite oxide. In the case of benzyl alcohol, interaction with epoxy groups was observed only for graphite oxide. A similar effect was caused by fillers on the process of matrix formation: in the presence of graphite fillers, the rate and heat effect of the reaction grow, and the gel point shifts to smaller times.
In essence, analogous data were reported by Mauro et al. [46]. These authors believe that a marked rise in the
On the other hand, it was found that the samples of graphite oxide with carboxyl or amino groups have almost no effect on the kinetics of nonisothermal curing of BADGE with 4,4'-diaminodiphenylmethane [47]. Possibly, this is related to a low concentration of the fillers (0.5%).
The effect of carbon nanofibers (diameter of 100–200 nm and length of 30–100 μm) oxidized in a solution of nitric acid and then treated with 3-glycidoxypropyltrimethoxysilanе on the kinetics of curing of epoxy resin Cycom 977 described by Eq. (1) was studied [48]. It was shown that all kinds of fibers exert a catalytic effect which manifests itself as an increase in ultimate conversion and growth of kinetic constants
The catalytic effect of a carbon nanofiber was observed: the ultimate conversion and the kinetic constants in Eq. (1) increase, while the respective activation energies decrease [49]. The higher activity is exhibited by fiber whose surface is modified through the oxidative polymerization of aniline (in accordance with the authors, the “nanograssy” coating).
The above results are rather contradictory, which is probably caused by ambiguity in the concentration of the filler, uncertainty in the degree of dispersion, and the magnitude and structure of its surface.
3.2 Noncarbon fillers: oxides of metals and silicon
The effect of Al2O3 nanoparticles on the kinetics of polycondensation of BADGE under the action of diethylenetriamine using modulated DSC was explored [50]. As a result, not only the rate of the process was registered, but also variation in the heat capacity of the system during the process was monitored. It was shown that the filler increases the rate of reaction but decreases the ultimate heat. Viscosity measurements confirmed that the formation of the polymer network accelerates in the presence of nanoparticles, and the gel point shifts not only with time but also with conversion. This implies that nanoparticles are directly involved in the formation of intermolecular bonds. At the same time, experiments with water additives revealed that nanoparticles affect the kinetics of the curing reaction in qualitatively the same manner as Al2O3 nanoparticle [51]. The authors inferred that water adsorbed by nanoparticles is responsible for the catalytic effect.
DSC was used to examine the effect of additives of Al2O3 and ZnO nanoparticles on the curing of BADGE with
At a fairly low concentration (1 and 5%), ZnO nanoparticles accelerate the reaction of BADGE with 2,2'-diamino-1,1'-binaphthyl; at concentration of 10%, their catalytic efficiency declines, while at content of 15%, retardation is observed [53]. Compared with the neat matrix, nanocomposites feature higher values of ultimate heat and glass-transition temperature with the maximum values corresponding to 5% content of nanoparticles. Probably, reduction in the catalytic activity of nanoparticles with increasing concentration may be attributed to their aggregation; as a result, the effective surface decreases.
Ghaffari et al. [54] studied how the size of ZnO nanoparticles affects the kinetics of BADGE curing with poly(aminoamide). Nanoparticles were sheets with a thickness of nearly 20–40 nm, while microparticles were rods with a length of ∼1 μm. Analysis was performed using Eq. (5). It was found that the autocatalysis of reaction is absent; that is,
BADGE with the propylenimine dendrimer carrying eight end groups -NH2 in the presence of Fe2O3 nanoparticles was cured [55]. The latter manifested the catalytic effect. The higher the concentration of nanoparticles, the more pronounced the increase in ultimate conversion and glass-transition temperature. It is shown that the kinetics of formation of the nanocomposite containing 10% Fe2O3 is adequately described by Eq. (2). No data are available for other systems, including the neat matrix. A similar result was reported in [56]. It was shown that the kinetics of curing of glycerol diglycidyl ether with 3,3'-dimethylglutaric anhydride in the presence of Al2O3 obeys Eq. (2).
Nanoparticles of metal oxides are able to adsorb components of the reaction system to one extent or another [57]. Possibly, their kinetic role is associated with this property.
Direct measurements of the complex specific heat capacity demonstrated that the interaction of SiO2 nanoparticles and BADGE molecules is very weak [58]. At all stages of polymer network formation, the interaction of nanoparticles and matrix is of a physical origin. The effect of the filler on the kinetics of curing was insignificant.
In contrast, acceleration of the process was observed [59, 60]. The kinetic studies revealed that the catalytic effect of SiO2 nanoparticles is related to the presence of hydroxyl groups on their surface [61]. When the latter groups are changed for epoxy groups, the effect of nanoparticles on the kinetics of BADGE reaction with
3.3 Minerals
For polymer nanocomposites, the most popular fillers from the class of minerals are layered silicates [62], which are sometimes called nanoclays, in particular, montmorillonite (MMT). The structure of its crystal lattice is such that it can adsorb various ions (mostly cations) and swell in polar liquids owing to their penetration into the interlayer space [63, 64].
At the nanometer scale, MMT is composed of three-layer stacks ∼0.7 nm in thickness and several hundred nanometers in length and width. At micron level, these stacks are united into primary particles with interlayer distance of about 1.35 nm. At higher level, they form aggregates. During formation of nanocomposites, stacks should be exfoliated in order to reach a high area of contact with the matrix. In order to facilitate exfoliation, the surface of stacks should be treated for the purpose of changing their hydrophilic nature to hydrophobic, because the hydrophilic character of the silicate surface hampers the dispersion of MMT. Neutral organic compounds may form complexes with interlayer cations; for example, alkylamines are transformed into alkylammonium cations. These properties of MMT govern the kinetic features of formation of epoxy nanocomposites.
In the absence of the curing agent (1,3-phenylenediamine), the modified MMT and even the unmodified MMT promote the homopolymerization of BADGE at a high temperature [65]. Depending on the nature of the intercalated modifier (octadecyl-, trimethylstearyl-, methyldihydroxyethylammonium), MMT may either catalyze the reaction of the epoxy oligomer or react with a prepolymer or a curing agent.
At the same time, it was found that MMTs modified with alkylamines weakly accelerate [66, 67, 68], retard [69], or do not affect at all [70] the kinetics of curing of epoxy oligomers with amines. A weak acceleration was also observed for the unmodified MMT and MMT with intercalated 3-aminopropylethoxysilane [71].
Thus, it should be stated that the rate of curing of epoxy oligomers is almost insensitive to the presence of MMT. However, the kinetics of formation of polymers is not reduced only to a change in the concentration of reactants: structure formation should be taken into account. Even to a higher extent, this applies to a nanocomposite, whose properties are determined not only by structural levels of polymer matrix but also by the structure of nanoparticles and the character of their distribution in the material bulk.
As was noted above, MMT requires exfoliation. Namely, this process occurs during the chemical reaction, and its efficiency depends on the reaction conditions. For example, it was shown [72] that the cationic polymerization of triglycidyl-
The optimum structure of epoxy composites was achieved when BADGE was cured with poly(ester diamine) in the nonisothermal regime at low rise in temperature (2.5 and 5 K/min) [73]. Small-angle X-ray scattering studies revealed the exfoliation of MMT in the matrix. The authors of [74] used hyperbranched polyethylenimine with end amino groups as a curing agent and attained effective exfoliation. A comparison of three systems, such as triglycidyl-
As was reported in [76], the nonisothermal curing of epoxy oligomers with amines in the presence of MMT includes four different reactions: formation of the matrix via the interaction of epoxy groups with the diamine curing agent, intracavity homopolymerization, and two homopolymerization reactions outside MMT which are catalyzed by onium ions of organically modified clay and tertiary amines.
X-ray diffraction was used to probe the exfoliation of MMT intercalated by octadecylammonium during the isothermal curing of BADGE with DDS [77]. It was shown that this process may be divided into three different stages (Figure 2).
The first stage is related to the penetration of BADGE into the interlayer space of MMT; at the second stage, the cationic polymerization of the epoxy resin catalyzed by ammonium takes place; and at the third stage, BADGE sorbed by MMT is cured with amine.
In order to identify the intracavity polymerization, mixture of MMT and triglycidyl-
An attempt to accomplish the intracavity polycondensation was made by Jagtap et al. [81]. In contrast to the commonly used MMT modifiers, i.e., polyalkylamines, they used half-neutralized salt of poly(ester diamine), which was intercalated via ionic exchange in an aqueous-organic solution, assuming that these macromolecules, when fixed by the ionic end on the walls of the cavity, will react with epoxy groups of the binder via its free amine end. However, no direct evidence for this reaction is available [81].
3.4 Metal-containing nanoparticles synthesized in situ
The synthesis of metal-containing nanoparticles for producing nanocomposites may be accomplished by various physical processes on the preformed matrix containing molecules of appropriate precursors [82, 83, 84, 85, 86, 87]. Physical methods of obtaining metal-containing nanoparticles (photolysis, radiolysis, and thermolysis) are as a rule accompanied by chemical reactions leading to their formation. An important factor is the diffusion of preformed substances (metal atoms): the glassy state of the matrix provides a considerable obstacle to diffusion. For example,
A substantially different method involves the combination of processes of formation of matrix and metal-containing nanoparticles, i.e., formation of nanocomposites in situ.
The main chemical method used at moderate temperatures includes the reduction of chemically bound metal atoms in nonpolar media. These methods of chemical reduction are the subject of most publications [83, 87, 89, 90, 91, 92, 93]. Mechanisms controlling formation of metal-containing nanoparticles in situ are highlighted in the review [94].
The transformation of the resulting single-valence atoms, or monomers, into nanoparticles includes nucleation stages with formation of primary clusters or stable particles, their growth by addition of monomers, possible subsequent coagulation, and/or Ostwald ripening. The kinetics of all these stages determines the size distribution function which strongly affects the ways and possibilities of the nanoparticles and corresponding nanocomposites’ application. An important role in this is played by a polymer medium in which chemical reactions take place, including the ability of its components or fragments of macromolecules to be adsorbed on the particles, as well as the possibility of formation of micelle-type structures.
With rapid decay of the precursor, there will be a supersaturation of the system with a monomer. In this case, in the first approximation, nucleation will be described by Gibbs-Volmer-Frenkel thermodynamic theory [95, 96], according to which the radius of the critical nucleus is determined by the formula:
where
A qualitative picture of nucleation kinetics on the basis of the classic thermodynamic notions was proposed by LaMer and Dinegar [97]. The pattern illustrating their idea is shown in Figure 3.
Rapid increase in the concentration of monomer will lead to the achievement of the critical value of
Although short spatial and temporal scales of the nucleation stage hamper the direct observation of the classic process, to trace the time-resolved formation of silver CNs using small-angle X-ray scattering in situ was managed [98]. Silver perchlorate was reduced with sodium boron hydride in an aqueous solution. As shown in Figure 4, the nanoparticles’ nucleation kinetics corresponds to the LaMer pattern: the number of particles initially grows without any appreciable change in their sizes, attaining a maximum in fractions of a second. Further, the number of nanoparticles descends, and their radius increases. This corresponds to stage III in the pattern, and nanoparticles interact with each other alongside with their simple growth via the reaction with monomers, i.e., the aggregation mechanism is engaged.
However, under conditions of formation of composites, it is hardly possible to implement such a mechanism. An alternative variant was obtained in [99]. When studying the synthesis of gold by reducing HAuCl4 with sodium citrate, it was shown that rapid nucleation is not observed; on the contrary, the kinetic curve of accumulation of critical nuclei is S-shaped with a more or less extended induction period. The authors suggested that such features of the process are due to redox reactions leading to the conversion of gold cations to a zero-valent atom and citrate ion to acetone dicarboxylic acid. In this case, the supersaturation of the system by the monomer, Au(0), is absent. Obviously, in this case the concept of a critical nucleus becomes meaningless.
Later it was established that S-shaped kinetics is inherent in many metals with variable valence (see, e.g., the review [100]). To describe such processes, a rather simple two-step scheme was proposed by Watzky and Finke [101]:
The first stage is the slow nucleation of “kinetically efficient” clusters 5Na3[(1,5-cyclooctadiene)Ir・P2W15Nb3O62], and
Studies of a wide range of systems show (see [94]) that the value depends on the number of catalytic active nuclei, namely, their ratio with increasing ratios
The processes of formation of zero-valence atoms or other monomers inevitably lead to their clustering. To stabilize clusters in a nonpolar solution, it is necessary to have amphiphilic molecules capable of forming adsorption layers and thereby form inverse micelles from the nanoparticles.
At the same time, when the epoxy nanocomposite films are stored under light for a while, the optical density
in which
Accordingly, the value of the limiting conversion of nanoparticles under light is higher than in dark: the conversion under light is 0.29, while in dark, the conversion is 0.11.
The decrease in
Although the mechanism of the DR process is not fully understood, there are grounds to believe that the equation proposed in [104, 105] for describing the kinetics of Ostwald ripening (OR) is applicable to DR. The latter is one of the options for the growth of the nanoparticles, when large particles grow at the expense of small particles. According to the theory, the change in the radius
where
As can be seen, the particles grow if
A vivid example of reversible OR and DR was demonstrated by Xin and Zheng [106]. They observed fluctuating growth of bismuth nanoparticles in the absence of precursor at 180°C. The reaction system consisted of a limited number of large Bi nanoparticles (80–150 nm in diameter) in a solution of oleylamine (surfactant) and dichlorobenzene. The Bi nanoparticles served as a source of monomeric Bi(0).
The process includes formation and growth of small particles due to large ones (DR) with simultaneous OR. The total number of particles increased for a while and then changed to the fluctuation mode. The total volume of content fluctuated near a certain level evidently given by the total volume of initial Bi nanoparticles. The size of each of the observed particles and their assemblies experienced similar fluctuations.
Obviously, the first stage of the DR process is the disassembly of small nanoparticles on zero-valence atoms and metal clusters. Under normal conditions, they subsequently lead to formation of nanoparticles, which require their diffusion displacement. But under the conditions of a glassy matrix, diffusion is difficult, if not forbidden at all. Therefore, the entire process is reduced to the first stage, i.e., “dissolution” of large nanoparticles with the formation of zero-valence atoms and silver clusters. The presence of a limit, apparently, is due to the saturation of the boundary zone surrounding the particle by the zero-valence atoms and clusters of silver formed.
As precursors soluble in organics, complexes of univalent gold [O(AuPR3)3](CF3SO3) (R = Ph or СН3) [107], [RN(CH3)3][Au(SC12H25)2] (R = C8H17, C12H25, and C14H29), and [(C18H37)2N(CH3)2][Au(SC12H25)2] were proposed by Nakamoto et al. [108]; salts of organic acids with a fairly bulky (even high-molecular-mass [109, 110, 111]) radical, such as silver myristate С13Н27СООAg, copper oleate (C18H33СОО)2Cu, silver oleate, silver octanoate C7H15COOAg, silver stearate C17H35COOAg, silver 2-hexyldecanoate
However, the nonideal state of solutions of these compounds should be taken into account. This implies that, when a certain concentration is exceeded, precursors in solution are united into associates, i.e., are clustered. Evidently, this circumstance cannot be disregarded when considering feasible mechanisms governing formation of metal-containing nanoparticles.
The silver nanoparticles by the reduction of alkyl carboxylates in trimethylamine at 78°C were synthesized [118, 119]. It was found that the induction period grows and the maximum rate decreases in the following sequence: decanoate, myristate, and stearate. But in this sequence, the length of the hydrocarbon radical of carboxylates (С9, С13, and С17) increases. It is reasonable to assume that solubility grows in the same sequence and, hence, the possibility of formation of clusters decreases. Thus, there is a direct relationship between the rate of formation of nanoparticles and the concentration of precursor clusters.
This idea underlies the theory of formation of metal-containing nanoparticles from precursors of the silver carboxylate type via their reduction which was put forth [120].
The model adopted for the formation of metal-containing nanoparticles may be presented as follows. Carboxylates reversibly form triangular and tetrahedral clusters. The development of larger clusters is not allowed because of steric reasons. The reduction of cation in them occurs. As a result, the adsorption of new salt molecules becomes possible. Indeed, if for carboxylates the tetrahedral structure is limiting, then the metal atom in the limit may be surrounded by 12 molecules (the icosahedron structure). It is assumed that the concentration of the reducing agent is high, so that the corresponding reaction is pseudo first order. Thus, the kinetic scheme may be written as follows:
where (
Here
A system of equations corresponding to scheme (11) was analyzed with a wide variation in kinetic constants. It was shown that the values of
The kinetics of the process is characterized by the existence of the induction period in the reaction of carboxylate consumption and an almost linear growth of average sizes of metal-containing nanoparticles with conversion. With the increase in constant
Papers addressing methods of in situ obtainment of epoxy nanocomposites with metal nanoparticles are scarce.
Under UV radiation, 2,2'-dimethoxy-2-phenylacetophenone decomposes into radicals. A dimethoxyphenyl-carbonium radical reacts with AgSbF6 and reduces a silver cation to Ag(0) via the transfer of electron, and then the radical transforms into the carbonium cation able to initiate the polymerization of diepoxide. Hence, silver nanoparticles and network matrix are formed simultaneously [121]. With increasing concentration of silver salt, the rate of polymerization and the ultimate conversion decrease, but the glass-transition temperature increases.
The silver nanoparticles with the same precursor, AgSbF6, were obtained but in the presence of degradable under irradiation with visible light 3,5-bis(4-methoxyphenyl)-dithieno[3,2-b;2,3d]-thiophene [122]. A similar technique was employed to synthesize epoxy nanocomposites with nanoparticles of silver [123] and gold [124], but 2,3-bornadione (camphorquinone) was used as a source of radicals; in the case of gold, the precursor was HAuCl4.
The silver nanoparticles in situ via the reduction of AgNO3 in the epoxy resin by Triton-100, which simultaneously functioned as a stabilizer of nanoparticles, were synthesized [125]. A cycloaliphatic epoxy resin, hexahydro-4-methylphthalic anhydride as a curing agent, a reducing agent, and a precursor were dissolved in acetonitrile and exposed to UV radiation. After completion of the process, the solvent was removed at a reduced pressure.
A complex of silver acetate and 2-ethyl-4-methylimidazole was synthesized in an epoxy resin, and during its curing Ag+ was reduced to Ag(0) as a result of thermal decomposition of the complex [126]. In such a manner, silver nanoparticles were generated in situ. The imidazole product of complex decomposition served as a curing agent.
The epoxy resin ED-20 with triethylamine in the presence of silver myristate was cured [127, 128, 129]. The reduction of the latter and the formation of silver nanoparticles occurred simultaneously during polymerization. Reduction agents were both amine and the epoxy group. Carboxylate groups compatible with the medium functioned as stabilizers of particles.
4. Conclusion
It has been shown that, regardless of whether a filler is introduced in the reaction system or is formed in situ during the process of matrix formation, its structure changes to a greater or lesser extent than the unfilled cured epoxy binder. In addition, the matrix influences the character of distribution of nanoparticles over volume. This effect is especially important in the case of graphene and MMT, when exfoliation is the case in point. The matrix governs the size and shape of the resulting nanoparticles. They interact with the epoxy matrix through the resulting interfacial layers. There is no doubt that all these factors affect the properties of the epoxy nanocomposites.
The application areas of composites are defined by both the physicomechanical parameters of the epoxy matrix, its strength, thermomechanical stability, and adhesion ability and the unique properties of nanoparticles.
Nanoparticles of gold, silver, copper, TiO2, ZnO, fullerene, and CNTs demonstrate effective antibacterial properties; therefore, composites containing these nanoparticles may be used for the microbiological control and purification of water, disinfection of surfaces, and creation of germicidal coatings, protective films, etc. Silver shows anti-inflammatory behavior and features antiviral and antifungal abilities. Its application in the form of nanoparticles (compared with the ionic form) decreases the cellular toxicity rather than the antibacterial efficiency [130].
Dielectric and magnetic epoxy nanocomposites have found wide use in such fields as Fourier spectroscopy, NMR, data storage, and absorption of electromagnetic radiation from other objects. The role of nanoparticles shows itself as improvement of electric strength and stress durability, suppression of space charge, and increase in the stability of dielectric discharge. For example, in the case of built-in planar capacitors, the insertion of dielectric films between copper sheets makes it possible to efficiently reduce the number of assembly devices. This not only leads to the miniaturization of circuit boards and electric wiring but also improves the characteristics of devices (e.g., promotes reduction in electromagnetic interference and switching noises) [131, 132, 133].
Epoxy resins are often employed in anti-wear applications. The use of such fillers as graphene oxide [134] or complexes MMT + SiO2 [135], even at their very low content, decreases the rate of material wear by almost an order of magnitude.
The epoxy binders modified with carboxylated carbon nanotubes are more resistant to the action of aging factors. The presence of aggregates of carboxylated carbon nanotubes in the epoxy matrix positively influences the preservation of physicomechanical properties of the composite subjected to heat and humidity aging. Microscopic examination revealed structural features of the epoxy nanocomposite and their effect on the resistance of the composite to the heat and humidity aging [136].
As for the use of epoxy nanocomposites in aerospace science and technology, this important problem, in author view, should be devoted to a special work. In short, it can be formulated as follows: structural nanocomposites, which are reinforcement structures based on carbon or glass fibers embedded in a polymer matrix modified with nanofillers, are the most important application of nanocomposites in the aerospace field [137], laminates, and sandwich structures. In addition, they can be used as anti-lightning [138], anti-radar [139] protection devices, flame retardant, and heat-resistant paints [140], ameliorating anti-corrosion performances [141].
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