Abstract
TG/FTIR/QMS-coupled method to study the thermal behavior along with the evolution of volatile decomposition products and thus the decomposition mechanism under inert conditions of some starch-g-poly(benzyl acrylate) copolymers was applied. Starch-g-poly(benzyl acrylate) copolymers under K2S2O8-initiated copolymerization process of benzyl acrylate monomer with gelatinized potato starch were prepared. The ATR-FTIR and 13C CP/MAS NMR confirmed the successful formation of grafted polymers with different grafting parameters such as grafting percent (%G) and grafting efficiency (%GE). The evolution of some physicochemical properties such as swelling, moisture resistance and chemical resistance allowed certifying that the copolymers obtained were more resistant toward polar solvents, moisture and acidic medium due to the incorporation of more hydrophobic chains into starch backbone as compared to unmodified potato starch. The TG/FTIR/QMS studies confirmed their similar thermal stability, two stage decomposition process but different and more complex decomposition mechanism under the second decomposition stage as compared to the previously presented starch-g-poly(benzyl methacrylate) copolymers.
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Introduction
The physical and chemical modification of naturally occurring polymers are the promising methods in order to prepare more environmentally friendly, inexpensive, biodegradable materials with improved or new properties as compared to unmodified materials [1–6]. The chemical modification methods allow modifying both physical and chemical properties of natural polymers [7–9].
Among various chemical modification methods, grafting is the method which is intensively studied and applied for the modification of carbohydrate structure from many years. It resulted in the preparation of novel materials where to the main polymer carbohydrate chain, one or more side chains through covalent bonds are connected. Depending on the applications of the graft copolymers, varying degree of hydrophilic- and hydrophobic-type vinyl monomers can be incorporated into polysaccharide matrix [10–13]. Generally, the graft copolymerization process starts in the formation of active sites on the polysaccharide backbone which are the result of abstraction of a hydrogen atom from hydroxyl groups leading to the production the polymer radicals which then participate in the grafting of vinyl monomers. Various initiating systems in order to produce polymer radicals can be applied in the grafting process. Generally, radical initiators such as ceric salts, persulfates, redox systems or others are used. In addition, besides chemical methods of initiations, free radicals on the polysaccharide backbone can be formed with ultraviolet, electron beam irradiation or 60Co [14–20]. Depending on the used initiating system, monomer type and its reactivity, polysaccharide type and other reaction conditions, the graft copolymers with different grafting parameters, various structure and thus various unique properties which can have a tremendous industrial potential as flocculants, supersorbents, sizing agents, thickeners and others can be prepared [21–26].
The present paper is the second part of our earlier studies [27]. The main objective of this paper was to study the thermal behavior, the type of volatile decomposition products, decomposition mechanism in inert atmosphere by applying TG/FTIR/QMS-coupled method of novel starch-g-poly(benzyl acrylate) copolymers obtained under K2S2O8-initiated grafting process of benzyl acrylate monomer onto gelatinized potato starch using the same synthesis conditions as previously applied, its structure by ATR-FTIR and 13C CP/MAS NMR, evaluation of their some physicochemical properties and comparison of the results obtained to those presented in Ref. [27].
Experimental
Materials
The starch-g-poly(benzyl acrylate) copolymers under potassium persulfate (Merck, Germany)-initiated copolymerization process of gelatinized potato starch (Melvit S.A., Poland) and benzyl acrylate monomer (obtained according to Ref. [28]) in the presence of nitrogen as an inert atmosphere according to the procedure described elsewhere [27] have been obtained.
Characterization of starch-g-poly(benzyl acrylate) copolymers
The grafting parameters such as grafting percent (%G) and grafting efficiency (%GE) were calculated using the equations given elsewhere [27, 29–31].
The ATR-FTIR spectra were carried out using a Fourier transform infrared (FTIR) spectrometer equipped with a diamond crystal (Tensor 27, Bruker, Germany). Each spectrum was gathered from 600 to 4000 cm−1 with a resolution of 4 cm−1.
13C CP/MAS NMR were collected with applying Bruker Avance 300MSL apparatus (Germany). All the spectra were gathered at the frequency of 75.5 MHz.
The swellability coefficients (B) of copolymers in polar (water, ethanol, butanol) and nonpolar (toluene, CCl4, hexane) solvents were determined by equilibrium swelling of the materials. B values were evaluated based on Eq. 1:
where V s—the volume of the copolymer after swelling, V d—the volume of the dry copolymer [27, 32, 33].
Percent moisture absorbance (%M) of copolymers was studied in an exsiccator where the 100 mg of dried samples was exposure to the water vapor at 25 °C for 24 h. %M was calculated from:
where m e—the final mass of the sample, m i—the initial mass of the sample [27, 33, 34].
The ca. 100 mg of the copolymers was treated with 1 M HCl and 1 M NaOH until a constant mass of the sample was reached. After filtration, washing with distilled water and drying at 60 °C, the residual was weighted and the chemical resistance toward basic and acidic media was calculated according to Eq. 3.
where m 1—the initial mass of the sample, m 2—the final mass of the sample [27, 35]. TG/FTIR/QMS-coupled method (STA 449 Jupiter F1, Netzsch coupled with TGA 585 Bruker spectrometer, Germany and QMS 403C Aëolos spectrometer, Germany) was applied in order to study the thermal properties of copolymers along with the evolution of volatile decomposition products and thus the decomposition mechanism of copolymers. In a typical procedure, ca. 10 mg of the sample was heated from 40 up to 750 °C with a heating rate of 10 °C min−1 in open Al2O3 crucible under inert conditions (helium, flow rate 40 mL min−1). The FTIR spectra of volatile decomposition products emitted under heating the copolymers, from 600 to 4000 cm−1 wave number with a resolution of 4 cm−1 were gathered. The QMS spectra in the range from 10 to 150 amu were collected.
Results and discussion
Characterization of starch-g-poly(benzyl acrylate) copolymers
The grafting parameters of the copolymerization process of benzyl acrylate monomer onto gelatinized potato starch backbone in the presence of K2S2O8 as an initiator in Table 1 are shown. According to the data presented, one can see that under changing the starch to monomer ratio from 1:0.25 to 1:1.5, the copolymers with different grafting percent (%G) can be prepared. As the starch to monomer ratio is increased from 1:0.25 up to 1:1.25, the grafting percent (%G) and grafting efficiency (%GE) are increased and then decreased imperceptibly. The results are in accordance with other previous study [27, 33] and confirmed that in order to prepare the starch-g-poly(benzyl acrylate) copolymers with high grafting parameters, the starch to monomer ratio should be above 1:1.
The ATR-FTIR and 13C CP/MAS NMR analyses were applied to confirm the grafting process of benzyl acrylate monomer onto starch backbone. The ATR-FTIR spectra of the example copolymer (copolymer 5) and non-modified potato starch are presented in Fig. 1. All the absorption signals responsible for the vibrations of atom groups which are present in the structure of non-modified potato starch (–OH, C–H, C–O stretching and C–H deformation) are clearly observed from the ATR-FTIR spectra [27, 33, 36]. However, after chemical modification of potato starch, the appearance of new absorption bands: two bands at 3034 and at 3067 cm−1 (CAr-H stretching), at 1728 (C=O stretching), two bands at 1452 and at 1496 cm−1 (aromatic C=C stretching) and two bands at 694 and 735 cm−1 (CAr-H out-of-plane deformation) [36] which directly confirmed the grafting of benzyl acrylate onto potato starch backbone is observed.
In addition, the structure of copolymers was identified based on 13C CP/MAS NMR spectra (Fig. 2). The solid-state NMR spectrum shows the resonance signals for all carbon atoms present in the structure of starch, at 94.2–100.5 ppm (C1), at 81.5 ppm (C4), at 72.3 ppm (C 2,3,5) and at 61.7 ppm (C6) [37–39]. Meanwhile, on the solid-state NMR spectra for copolymers, new, additional resonance signals centered at 40.8 ppm (C at –CH–CH2–) n groups), at 128.5–136.4 ppm (C in aromatic rings) and at 175.2 ppm (C in C=O) are appeared. When we are comparing, the 13C CP/MAS NMR spectra before and after chemical modification of potato starch, it is worth noticing that the fall in the intensity of the C2, C3 and C6 carbon signals after grafting process is observed. It can be testified that both, primary and secondary hydroxyl groups of starch participate in the grafting process [37]. In addition, also, the changes in the intensity for C4 and C1 carbon signals for starch which may be due to the partial hydrolysis of glycosidic bonds under the preparation of copolymers were indicated [40].
Properties of starch-g-poly(benzyl acrylate) copolymers
The starch-g-poly(benzyl acrylate) copolymers are insoluble materials in available organic solvents. However, due to their variable hydrophilic-hydrophobic properties, the copolymers demonstrate various swelling in polar and nonpolar solvents, Fig. 3. According to Fig. 3, the copolymers are the materials which swelling is restricted in polar solvents such as water, ethanol and butanol as compared to non-modified potato starch. However, their swelling in nonpolar solvents (toluene, CCl4, hexane) is higher as compared to non-modified potato starch. Such behavior is connected with the modification of potato starch backbone by hydrophobic poly(benzyl acrylate) chains and is in accordance with our previous studies [27, 33]. In addition, due to the lower amount of hydroxyl groups in the structure of copolymers, the copolymers are more moisture restricted than potato starch. The percent moisture absorption changes from 40 up to 20 % as the grafting percent is increased [27, 33] (Fig. 4).
The chemical resistance studies demonstrated that starch-g-poly(benzyl acrylate) copolymers were not resistant to basic environment. All the copolymers are fully gelated in 1 M NaOH medium. However, the copolymers prepared were more restricted to the acidic environment. The mass loss in 1 M HCl medium ranges from 31 to 34 %, and it was almost independent on the grafting percent (Table 2).
Thermal properties of copolymers
The characteristic TG/DTG curves of starch-g-poly(benzyl acrylate) copolymers are presented in Fig. 5. The T max, mass loss (Δm) and residual mass at 740 °C (rm) are collected in Table 3. Thermogravimetric analysis of copolymers revealed two major, non-well separated decomposition stages between temperatures of ca. 200 °C up to ca. 560 °C. Meanwhile, the mass loss of copolymers ranges from ca. 0.5 % to ca. 1.7 % at temperatures below 200 °C which was directly connected with the evaporation of moisture from copolymers under heating. However, the first decomposition stage of copolymers occurs at temperatures from ca. 200 °C to ca. 335 °C with T max1 288–292 °C and corresponds to a mass loss from 45.7 up to 33.7 % of the mass initially present. The second decomposition stage between ca. 335 and 560 °C with T max2 388–395 °C and mass loss from 25.5 to 46.1 % was happened. In addition, regarding to our previous study [27], the same relationship between grafting percent and mass loss under the first and second decomposition stages was indicated. Higher grafting percent was resulted in lower mass loss under the first decomposition stage but higher mass loss under the second decomposition stage. The heating of copolymers above temperature of 560 °C was resulted in further slow mass loss without the appearance of the DTG signal. The mass loss didn’t exceed 2.5 % in the temperature range of 560–740 °C. The TG/DTG studies confirmed that the decomposition process of copolymers under inert conditions was not full. After heating of the materials up to 740 °C, the residual mass corresponded to 25–15.5 % of the initial sample mass was indicated.
TG/FTIR/QMS studies
TG/FTIR/QMS-coupled method was applied to describe and evaluate the degradation mechanism of starch-g-poly(benzyl acrylate) copolymers. The FTIR spectra of the volatile decomposition products emitted under decomposition of copolymers (from ca. 200 to 740 °C) in inert conditions for copolymers with different grafting percent are presented in Fig. 6.
The FTIR spectra gathered at the temperature range 200–330 °C (first decomposition stage) are a typical spectra for the volatile decomposition products which are created under decomposition of starch from starch-g-poly(benzyl acrylate) copolymers which is in accordance with other studies [33, 41–43]. It confirmed that starch is a less thermally stable polymer as compared to benzyl acrylate chains grafted and decomposed mainly through the cleavage of glycosidic bonds, strong bonds and thermal dehydration processes forming as main gaseous decomposition products CO, CO2, H2O, aldehydes, alcohols, acids, aliphatics and furanes fragments [33, 41–43]. Thus, the thermal decomposition of starch from starch-g-copolymers results in the liberation of the polymer grafted from the copolymers which needs higher temperature in order to decompose. On the FTIR spectra collected at temperature range 330–460 °C (second decomposition stage), it is well visible the presence of the absorption bands characteristic for the stretching vibrations of –OH (3570–3730 cm−1), the stretching vibrations of CAr-H and =C–H (3037–3070 cm−1), the stretching vibrations of C–H in –CH2– (sym 2873 and asym 2931 cm−1), the stretching vibrations of C–H in O=C–H (2720 and 2780 cm−1), the stretching vibrations of C=O (1733 cm−1 with a shoulder at 1780 cm−1), the stretching vibrations of aromatic C=C (1492 and 1594 cm−1), the deformation vibrations of C–H (1378–1446 cm−1), the stretching vibrations of C–O (1012–1280 cm−1) and out-of-plane deformation vibrations of =C–H and CAr-H (694–902 cm−1). Besides those above bands, the bands responsible for the vibrations of CO (2000–2200 cm−1), CO2 (670 and 2330–2365 cm−1) and H2O (above 3500 cm−1) [42, 43] are well documented on the FTIR spectra. Regarding the occurrence of the characteristic absorption signals on the FTIR spectra under the second decomposition stage and the structure of poly(benzyl acrylate), it can be suspected that the main decomposition processes are the result of the both random main-chain scissors and side-chain scissors [44, 45], as it is presented in Scheme 1. As a result the mixture of organic and inorganic volatile decomposition products is emitted under the second decomposition stage. Among them, the most feasible organic volatile decomposition products are alkene, aromatic, alcohol, aldehyde, acid or cyclic ketone fragments and benzyl acrylate monomer as it is shown in Scheme 1.
The further heating of the residue formed above 460 °C resulted in the emission of CH4 (3014 cm−1), CO (2000–2200 cm−1), H2O (above 3500 cm−1) [42, 43, 46–49] and some of the other less volatile organic fragments. According to the FTIR spectra gathered at temperatures higher than 460 °C, the appearance of the small intensity signals responsible for the stretching vibrations of CAr-H and =C–H (3037–3070 cm−1), the stretching vibrations of C–H (2873–2931 cm−1), the stretching vibrations of C=O (1733 cm−1), the deformation vibrations of C–H (1378–1446 cm−1), the stretching vibrations of C–O (1012–1280 cm−1) and out-of-plane deformation vibrations of =C–H and CAr-H (694–902 cm−1) which can be due to the emission of mainly alkene, aromatic, alcohol or ketone fragments is observed. The type of the decomposition products emitted at higher temperatures may indicate on the further secondary reactions between the decomposition products and/or residue formed [27].
Additionally performed QMS analysis directly confirmed the FTIR results. Due to the same volatile decomposition products emitted under heating of all copolymers studied, the exemplary QMS spectra gathered at the first decomposition stage (200–330 °C), at the second decomposition stage (330–460 °C) and above 460 °C are presented in Fig. 7. The appearance of m/z ions typical for the gaseous products evolved under decomposition of potato starch from the copolymers studied under the first decomposition stage was indicated. One can clearly see the presence of m/z ions characteristic for CO2 (44), CO (28), H2O (18,17,16) and organic fragments: furanes (50, 51, 52, 53, 68, 69, 82, 95, 96), aldehydes (15, 26, 28, 29, 30, 41, 42, 43), alcohols (31, 45, 29, 27, 46, 43, 26, 30), acids (13, 28, 29, 30, 41, 42, 43, 45, 46) and aliphatics (30, 29, 28, 27, 26) [50]. However, on the QMS spectra for copolymers gathered at the second decomposition stage, the formation of organic fragments such as benzaldehyde (m/z: 77, 106, 105, 51, 50, 78, 52, 74, 107, 39), benzyl alcohol (m/z: 79, 108, 107, 77, 51, 91, 78, 50, 39, 80), cyclobutanone (m/z: 42, 70, 41, 39, 27, 26, 43, 14, 38, 28), glutaric anhydride (m/z: 42, 70, 44, 41, 27, 39, 26, 43, 40, 29), glutaric acid (m/z: 86, 42, 45, 55, 60, 41, 58, 39, 43, 114), dienes (m/z: 79, 80, 77, 39, 51, 78, 50, 52, 27, 38), benzyl acrylate (m/z: 91, 55, 117, 90, 107, 79, 77, 65) and inorganic species (CO2, CO, H2O) indicated mainly on the decomposition process of poly(benzyl acrylate) from the copolymers. The heating of copolymers above the temperature of 460 °C resulted in the emission of CH4 (16, 15, 14, 13), CO (28), H2O (16, 17, 18) and some amount of organic products, among them the most feasible were aromatic fragments: (m/z: 77, 79, 106, 105, 51, 50, 78, 80, 91, 108, 52, 74, 107, 39), dienes (m/z: 79, 80, 77, 39, 51, 78, 50, 52, 27, 38) and ketones (m/z: 42, 70, 41, 39, 27, 26, 43, 14, 38, 28) [50].
The TG/FTIR/QMS data confirmed that the decomposition mechanism of starch-g-poly(benzyl acrylate) copolymers was completely different and more complex as compared to the decomposition mechanism of the previously studied starch-g-poly(benzyl methacrylate) copolymers [27].
Conclusions
The ATR-FTIR and 13C CP/MAS NMR analyses confirmed the successful preparation of starch-g-poly(benzyl acrylate) copolymers under the grafting process of benzyl acrylate monomer onto gelatinized potato starch backbone in the presence of K2S2O8 as an initiator. The copolymers obtained were characterized by lower swelling in polar than in nonpolar solvents and higher moisture resistant than non-modified potato starch. Their swelling and moisture resistance were directly depended on the grafting percent which was in accordance with our previous results. However, the chemical resistance of starch-g-poly(benzyl acrylate) copolymers was completely different as compared to previously described starch-g-poly(benzyl methacrylate) copolymers. The starch-g-poly(benzyl acrylate) copolymers were gelatinized completely when treated with basic medium. In addition, their resistance toward acidic medium was almost independent on the grafting percent. The thermal stability and the decomposition course of starch-g-poly(benzyl acrylate) and starch-g-poly(benzyl methacrylate) copolymers were similar. The first decomposition stage of copolymers was connected with the cleavage of glycosidic bonds, strong bonds and thermal dehydration processes of starch from copolymers which resulted in the emission of the typical for starch gaseous decomposition products such as CO, CO2, H2O, aldehydes, alcohols, acids, aliphatics and furanes fragments. Meanwhile, the second degradation stage of copolymers was run through completely different and more complex mechanism as compared to starch-g-poly(benzyl methacrylate) copolymers as it was confirmed by applying the TG/FTIR/QMS-coupled method. Under this decomposition stage, random main-chain scissors and side-chain scissors were happened which caused the formation of the mixture of inorganic and organic species such as CO, CO2, H2O, alkene, aromatic, alcohol, aldehyde, acid or cyclic ketone fragments and benzyl acrylate monomer.
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Worzakowska, M. Thermal behavior, decomposition mechanism and some physicochemical properties of starch-g-poly(benzyl acrylate) copolymers. J Therm Anal Calorim 126, 531–540 (2016). https://doi.org/10.1007/s10973-016-5603-7
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DOI: https://doi.org/10.1007/s10973-016-5603-7