Volume 23, Number 5, September-October 2016
|Number of page(s)||7|
|Section||Dossier: New perspectives of European oleochemistry / Les nouvelles perspectives de l’oléochimie européenne|
|Published online||21 June 2016|
A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis
Une approche plateforme de l’huile de cardanol : de la synthèse d’intermédiaires réactionnels à la synthèse de polymères
Institut Charles Gerhardt Montpellier, UMR 5253, CNRS-Université de Montpellier, ENSCM, 8, Rue de l’École Normale, Montpellier, France
* Correspondence: firstname.lastname@example.org
Received: 16 March 2016
Accepted: 11 May 2016
This review proposes a platform approach for the synthesis of various building blocks from cardanol oil in one or two-steps synthesis. Cardanol is a natural phenol issued from Cashew nutshell liquid (CNSL). CNSL is a non-edible renewable resource, co-produced from cashew industry in large commercial volumes. Cardanol is non-toxic and particularly suitable as an aromatic renewable resource for polymers and materials. Various routes were used for the synthesis of di- and poly-functional building blocks used thereafter in polymer syntheses. Phenolation was used to dimerize/oligomerize cardanol to propose increase functionality of cardanol. Thio-ene was used to synthesize new reactive amines. Epoxidation and (meth)acrylation were also used to insert oxirane or (meth)acrylate groups in order to synthesize polymers and materials.
Cet article présente une approche plateforme de synthèse d’intermédiaires réactionnels variés pour l’élaboration de polymères à partir de cardanol. Le cardanol est un phénol naturel issu de l’huile de coque de noix de cajou – Cashew nutshell liquid (CNSL), une ressource renouvelable non-alimentaire coproduit de l’industrie de la noix de cajou. Le cardanol est non-toxique est particulièrement adapté pour l’intégration de noyaux aromatiques dans des polymers et des matériaux biosourcés. Différentes voies ont été envisages pour la synthèse d’intermédiaires réactionnels di- et poly-fonctionnels pour la synthèse de polymères. La phénolation a été utilisée pour dimériser/oligomériser le cardanol pour augmenter sa fonctionnalité Le couplage thio-ene a été utilize pour élaborer de nouvelles amines réactives. L’époxidation et la (méth)acrylation ont permis la fonctionnalisation groupes oxirane ou (méth)acrylate afin d’élaborer des matériaux.
Key words: Cardanol / epoxide / acrylate / carbonate / amine / vinyl ester
Mots clés : Cardanol / epoxy / acrylate / carbonate / amine
© F. Jaillet et al., published by EDP Sciences, 2016
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
A large part of key commercial chemicals are aromatic substances and are derived from petrochemical resources (Tuck et al., 2012). In the recent years, the demand for renewable resource-derived polymers have increased dramatically owing to increasing environmental concern and restricted availability of fossil resources (Gandini, 2011). Most recently, much focus was put on biobased thermosetting resins such as epoxy resins, phenol resins, unsaturated polyesters and biocomposites. This is particularly due to their difficulty to be recycled owing to their infusibility and insolubilty (Koike, 2012). Literature reports very interesting pieces of works dedicated to the use of natural flavonoids (Benyahya et al., 2014) or lignin-derivatives such as vanillin (Fache et al., 2014). However, these resources exhibit strong drawbacks such as a low purity and high molar masses that reduices their industrial development. Moreover, the depolymerization of lignin remains challenging (Brazinha et al., 2011; Carrier et al., 2011). Thus, cardanol is gaining an increasing interest as natural source of phenol (Balachandran et al., 2011). Cardanol is produced from cashew nut shell liquid (CNSL), directly extracted from the shell of the cashew nut, fruit from cashew tree, anacardium occidentale, mostly grown in India, East Africa and Brazil (Ionescu et al., 2012). The global production of CNSL approaches one million tons annually (Campaner et al., 2009) and CNSL became of the few major and economic sources of naturally occurring phenols. This really promising aromatic renewable source represents a good natural alternative to petrochemicals derived phenols (Pillail et al., 1990). CNSL constitutes approximately 25% of the total weight of the cashew nut and is composed of anacardic acid (3-n-pentadecylsalicylic acid) and smaller amounts of cardanol (3-n-pentadecylphenol), cardol (5-n-pentadecylresorcinol), and methylcardol (2-methyl-5-n-pentadecylresorcinol) – the long aliphatic side-chain being saturated, mono-olefinic (8), di-olefinic (8, 11), and tri-olefinic (8, 11, 14) with an average value of two double bonds per molecule (Fig. 1). The thermal treatment of CNSL followed by a distillation lead to the decarboxylation of anacardic acid that yields an industrial grade of cardanol (about 90%), with a small quantity of cardol and methylcardol (Phani et al., 2002; Carioca et al., 2005). Cardanol is a yellow pale liquid composed of four meta-alkyl phenols differing by unsaturation degree of aliphatic chain: saturated chains (SC) 8.4%, monoolefinic (MO) 48.5%, diolefinic (DO) 16.8% and triolefinic (TO) 29.33% chains (Sultania et al., 2011; Tyman et al., 1975).
Different molecules of CNSL, mono-olefinic (8), di-olefinic (8,11), and tri-olefinic (8,11,14).
Cardanol was already extensively studied for the synthesis of monomers and polymers particularly by Wadgaonkar et al. (More et al., 2001; Sudhakar et al., 2009). Hence, it was used in direct polymerization (Kim et al., 2005), as a polyol for the synthesis of new polyurethanes (Suresh et al., 2005), in polyester formulations (Lespinasse et al., 2011), in thermosets (such as Novolac) (Yadav et al., 2009; Huong et al., 1996), in vinyl ester networks (Sultania et al., 2010) and also in epoxy networks modification (Unnikrishnan et al., 2008).
Our team published a comprehensive review on the functionalization of cardanol for the synthesis of monomers, polymers and additives (Voirin et al., 2014). Moreover, we synthesized new building blocks from cardanol 1 in one or two step synthesis by various reactions (Jaillet et al., 2015), such as thiol-ene coupling, allylation, epoxidation, carbonation or acrylation (Scheme 1). These reactions lead to di- and polyepoxide monomers 2, 3 (Jaillet et al., 2013), mono- or di-(meth)acrylic monomers 4 (Jaillet et al., 2014, 2016) and carbonate 5 by carbonation reaction (Besse et al., 2013), primary amines 6, 7 (Darroman et al., 2014). All these building blocks were used for the synthesis of various polymers such as polyurethanes (PUs), non-isocyanate polyurethanes (NIPUs), vinyl esters and epoxy networks (Darroman et al., 2015, 2016).
Synthesis of various building blocks from cardanol.
Synthesis of epoxided cardanol with epoxidation yields.
Few works reported the direct epoxidation of cardanol for the synthesis of new epoxy networks phenol of cardanol was epoxidized with epichlorohydrin (Verneker et al., 1980; Baker et al., 1955) in basic conditions, with ZnCl2, at 95 °C. This product is commercialized by Cardolite Coporation. A patent claims also the use of commercial epoxidized cardanol (Agarwal et al., 2003). Furthermore, the epoxidation of double bonds of cardanol was also carried out with perbenzoic acid by Patel et al. (Patel et al., 1989) and by Greco et al. (Greco et al., 2010). Suresh (Suresh, 2013) performed this reaction with performic acid. Moreover, the epoxidation of these double bonds could also be performed with enzymes such as Candida Antarctica lipase (yield 95%) (Kim et al., 2007). Additionally, polyepoxy cardanol was synthesized by direct polymerization of double bonds of epoxidized cardanol followed by reaction with various amines (Kanehashi et al., 2013). All these studies that report the epoxidation of cardanol neither really described the composition of products of epoxidation reaction nor investigated the properties of synthesized epoxy materials. Indeed, epoxy networks are a major class of thermoset polymers, with a global production around 2Mt/y (Shen et al., 2009). Epoxy polymers are extensively used as coatings, adhesives and in structural applications owing to their outstanding mechanical and electrical properties, chemical resistance and adhesion (May, 1988). Diglycidyl ether of bisphenol A (DGEBA) is nowadays the most used monomer for the synthesis of epoxy polymers and materials. DGEBA is synthesized by epoxidation of bisphenol A (BPA). Indeed, the aromatic ring of BPA is particularly interesting since it confers good thermal, chemical and mechanical resistance to epoxy polymers. But this endocrine disruptor mimic the body’s own hormones and may lead to several negative health effects (Gor, 2007; O’Connor and Chapin, 2003; Okada et al., 2008; Vom Saal and Myers, 2008). Thus, a recent review of studies of low-dose effects of BPA found that 94 out of the 115 publications reviewed reported significant effects, including alterations in brain chemistry and structure, behavior, immune system, enzyme activity, male and female reproductive system in a variety of animals, including snails, fish, frogs and mammals (Vom Saal and Hughes, 2005). The negative impact of BPA on human health and environment necessarily implies the elimination of BPA especially since some countries, such as Canada or France, have recently banned the use of BPA in food contact materials. Therefore there is an increasing interest of chemical industry for non-harmful aromatic substituents to BPA, especially for the synthesis of epoxy polymers Thus, cardanol could be an interesting substitute to BPA in some polymers such as epoxy polymers. In this context, our team synthesized new building-blocks from cardanol in order to synthesize biobased epoxy networks.
The aim of the work reported herein was to synthesize fully biobased aromatic epoxide monomers from cardanol. Even if epoxidation of cardanol was already studied, we both synthesized a polyfunctional epoxyded cardanol and deeply analyzed composition of commercial NC514 epoxidized cardanol, which was never reported in literature to the best of our knowledge. First, we increased the number of double bonds of cardanol by quantitative allylation of phenol groups with allyl bromide. Thus, we obtained an average number of 3 double bonds per cardanol molecule. Then we epoxidized the double bonds and compared the use of both meta-chloroperbenzoic acid mCPBA and H2O2, owing to previously reported routes (Aouf et al., 2013; Sato et al., 1996).
We obtained various results owing to position of double bonds and epoxidation routes (Scheme 2). Indeed, terminal double bonds are not epoxided by mCPBA, whereas epoxidation yield is 25% for terminal double bonds with H2O2. Internal 11,12 double bonds are nearly quantitatively epoxided by mCPBA and fully epoxided with H2O2. Concerning internal 8,9 double bonds, epoxidation yield is 77% with mCPBA and quantitative with H2O2. Concerning allylic double bonds, epoxidation is quantitative with mCPBA, and epoxidation yield is only 77%, with H2O2. Anyway, a complete epoxidation of all double bonds of cardanol is not possible, which could be a drawback for further use in polymerization. Therefore the diepoxided cardanol NC-514 proposed by Cardolite is an interesting alternative. It is synthesized in two steps by phenolation of aliphatic chain, prior to reaction of phenol hydroxyl groups with epichlorohydrin (Ionescu and Petrovic, 2011). Thus, we thoroughly analyzed the composition of epoxidized cardanol NC-514 supplied by Cardolite. Thesupplier indicates an EEW of 400 g/eq and following chemical structure of diepoxided cardanol (Fig. 2).
Chemical structure of NC-514.
The epoxided cardanol NC-514 was extensively studied in a previous paper from our team using 1H- and 13C-NMR, size exclusion chromatography and titration (Jaillet et al., 2013). It was shown that NC-514 contains saturated and mono-olefinic chains with a respective composition of 95% saturated chains and 5% mono-olefinic chains. 1H-NMR calculations allow determining a functionality of 2.3 epoxy groups per molecule. It was also demonstrated that NC-514 has a macromolecular structure: the experimental molar mass of NC-514 is 1029 g/mol (dispersity of 2.16), which is far higher than the idealized molar mass of about 460 g/mol. The most likely chemical structure of NC-514 after extensive characterization is the one proposed in Figure 3. The phenol groups are respectively in position (8), (8, 11) or (8, 11, 14).
Likely chemical structure of cardanol NC-514.
Epoxy networks were formulated with various epoxide monomers and amines. We tested cardanol NC-514 (Scheme 1, 3) and diglycidyl ether of bisphenol A (DGEBA) with isophorone diamine (iPDA), cardanol NX-5454 (Scheme 1, 6) and synthesizd cardanol cysteamine (Scheme 1, 7). Epoxy formulations were stirred 3 min at room temperature and put in a mold at 120 °C during 5 h, then at 170 °C during 30 min. Five different formulations were carried out with various ratios: DGEBA/iPDA, cardanol NC-514/iPDA, cardanol NC-514/Jeffamine D400, cardanol NC-514/Cardanol NX-5454 and cardanol NC-514/cardanol cysteamine.
Thermal and mechanical properties of epoxy polymers from cardanol.
The polymers synthesized with epoxidized cardanol NC-514 exhibit lower Tg values than with DGEBA, due to the long aliphatic chain of cardanol. All epoxy networks exhibit very interesting thermal stabilities. The mechanical properties for NC-514 are lower than for DGEBA however the moduli recorded could be interesting for coating applications (Table 1).
Synthesis of cardanol (idealized structure) methacrylated VE prepolymer.
Vinyl ester (VE) networks are one of the most important classes of thermoset polymers, with a global production of 1 Mt/y, combining chemical, mechanical and thermal properties of epoxy networks with rapid cure of unsaturated polyesters (UP). Therefore VE are used for various industrial applications such as surface coatings, adhesives, radiation curable inks, printed circuit board coatings, spherical lens materials and composites (Agrawal et al., 2003; Gaur et al., 1993). VE prepolymers are synthesized by reaction between epoxy monomers and (meth)acrylic acid. The most commonly used epoxy monomer for the synthesis of VE prepolymers is DGEBA. DGEBA is methacrylated by reaction with methacrylic acid to yield methacrylated diglycidyl ether of bisphenol A (MDGEBA). By means of the two terminal reactive double bonds, MDGEBA can easily yield cross-linked network structures by a free-radical polymerization mechanism. Due to the high viscosity of VE prepolymers, it is necessary to add some vinyl monomers as reactive diluents (such as styrene, acrylates or methacrylates) (Agrawal et al., 2003; Gaur et al., 1993) that copolymerize with VE prepolymers. Styrene is highly polymerizable with acrylate or methacrylate functions. MDGEBA is the most commonly used prepolymer since it allows to obtain vinyl ester materials with styrene as reactive diluent, exhibiting good thermal resistance and mechanical properties. The main issues of vinyl esters concern the use of MDGEBA as prepolymer, since it is derived from bisphenol A. Indeed, bisphenol A is classified as carcinogenic, mutagenic, reprotoxic (CMR). Literature reports interesting studies on the replacement of MDGEBA prepolymer for VE networks. Thus, the use of isosorbide diglycidyl ether (Lukaszczyk et al., 2012; Sadler et al., 2013; Chrysanthos et al., 2011) or furfuryl derivatives (Jeong et al., 2013) was reported, but the properties of obtained materials do not meet the needed thermal properties for targeted applications. The synthesis of VE networks from vegetable oils is also reported in literature. Thus, La Scala et al. proposed the functionalization of vegetable oils with methacrylic functions in order to obtain materials with Tg values around 70 °C (La Scala et al., 2004). Furthermore, Adekunle et al. reported the functionalization of epoxidized soybean oil with methacrylic acid or methacrylic anhydride to obtain biobased composites (Adekunle et al., 2010). Recently, Webster et al. reported the methacrylation of epoxidized sucrose soyate to yield thermoset materials with high properties (Yan et al., 2014).
The esterification reaction of epoxided cardanol NC-514 was carried out with methacrylic acid using TPP as catalyst and hydroquinone as inhibitor at 80 °C, as shown in Scheme 3 to yield cardanol methacrylated VE prepolymer (CMAVE).
The cardanol-based VE prepolymer (CMAVE) and the DGEBA-based VE prepolymer (BMAVE) were prepared as described earlier (Jaillet et al., 2014). Then, they were diluted in styrene (ST) or isobornyl methacrylate (IBOMA) reactive diluents (ratio prepolymer/reactive diluent 60/40) and cured 12 h at 120 °C and 2 h at 150 °C using 3% of tert-butyl peroxybenzoate (Trigonox C) as initiator to yield the VE networks: cardanol-based methacrylated VE networks CMAVE/ST, and CMAVE/IBOMA and the DGEBA-based methacrylated VE networks BMAVE/ST and BMAVE/IBOMA. There is no difference of crosslinking rate between VE with styrene and IBOMA. Each VE had a gel time around 30 min.
All networks were stable up to 300 °C and started losing weight above this temperature. Rapid decomposition was then observed in the temperature range of 400 °C and almost total volatilization of the sample was occurred around 500 °C. These results showed the similar thermal stability of cardanol-based (Fig. 4) and DGEBA-based VE networks under nitrogen atmosphere. Dynamic scanning calorimetry (DSC) studies were performed to study the glass transition temperature of the cured VE networks. The T values are reported in Table 2 Complete crosslinking of the DGEBA-based and cardanol-based VE resins by the cure procedure was ensured since no exothermal cross-linking peak was observed during the first heating ramp. Indeed, the aliphatic chain of cardanol confers higher mobility to the chains, which leads to lower Tg. However, higher Tg was obtained with IBOMA reactive diluent compared to styrene because the isobornyl bis-cyclic group is much more bulky and rigid than benzene ring. Thermomechanical properties of the cured VE networks were determined using dynamic mechanical analysis (DMA).
Thermal and mechanical properties of VE from cardanol.
Similarly, Tα of cardanol-derived VE are lower than the ones of MDGEBA-derived VE. However, Tα obtained with IBOMA are very interesting for composite applications. The mechanical properties for cardanol-derived VE are a bit lower than for DGEBA. However the moduli recorded could be interesting for composite applications.
Cardanol-derived VE network.
We developed a chemical toolbox based on phenolation, epoxidation, oxidation, acrylation, carbonation and amination to synthesize a library of biobased building blocks with various functions from cardanol derived from cashew nutshell liquid. The synthesized building blocks reported in this contribution are polyfunctional phenols, epoxides, amines and cyclocarbonates. They could lead to polymers such as polyurethanes, polyhydroxyurethanes, epoxy resins and vinyl esters. Thus, we synthesized partial and fully cardanol-derived epoxy materials from epoxidized cardanol and cardanol amines. These epoxy polymers are very interesting since they bear aromatic rings for interesting formulation. We obtained different mechanical and thermal properties owing to the various formulations. We demonstrated that cardanol-derived epoxy polymers could find promising properties for coatings applications. Indeed, cardanol is a promising non-edible biobased aromatic resource for polymer applications.
- Adekunle K, Åkesson D, Skrifvars M. 2010. Synthesis of reactive soybean oils for use as a biobased thermoset resins in structural natural fiber composites. J. Appl. Pol. Sci. 115: 3137–3314. [CrossRef] [Google Scholar]
- Adekunle K, Åkesson D, Skrifvars M. 2010. Biobased composites prepared by compression molding with a novel thermoset resin from soybean oil and a natural-fiber reinforcement. J. Appl. Pol. Sci. 116: 1759–1765. [Google Scholar]
- Agarwal RK, Bammel BD, Fristad WE, Rossier GW, Siebert EJ, Yang Z. 2003. Resin-based Autodeposition Coatings. US Patent 0104212. [Google Scholar]
- Agrawal S, Mishra A, Rai JSP. 2003. Effect of diluents on the curing behavior of vinyl ester resin. J. Appl. Pol. Sci. 87: 1948–1951. [CrossRef] [Google Scholar]
- Aouf C, Nouailhas H, Fache M, Caillol S, Boutevin B, Fulcrand H. 2013. Multi-functionalization of gallic acid. Synthesis of a novel biobased epoxy resin. Eur. Pol. J. 49: 1185–1195. [CrossRef] [Google Scholar]
- Baker NF. 1955. Epoxy resin compositions, US Patent 824 302. [Google Scholar]
- Balachandran VS, Jadhav SR, Vemula PK, John G. 2012. Recent advances in cardanol chemistry in a nutshell: from a nut to nanomaterials. Chem. Soc. Rev. 42: 427–38. [CrossRef] [Google Scholar]
- Benyahya S, Aouf C, Caillol S, Boutevin B, Fulcrand H. 2014. Functionalized green tea tannins as phenolic prepolymers for bio-based epoxy resin. Ind. Crops Prod. 53: 296–307. [CrossRef] [Google Scholar]
- Besse V, Auvergne R, Carlotti S, Boutevin G, Otazaghine B, Caillol S, Pascault JP, Boutevin B. 2013. Synthesis of isosorbide based polyurethanes: an isocyanate free method. React. Funct. Pol. 73: 588–594. [CrossRef] [Google Scholar]
- Brazinha C, Barbosa DS, Crespo JG. 2011. Sustainable recovery of pure natural vanillin from fermentation media in a single pervaporation step. Green Chem. 13: 2197. [CrossRef] [Google Scholar]
- Campaner P, D’Amico D, Longo L, Stifani C, Tarzia A. 2009. Cardanol-based novolac resins as curing agents of epoxy resins. J. Appl. Pol. Sci. 114: 3585–3591. [CrossRef] [Google Scholar]
- Carioca JOB, Vasconcelos GFC, Abreu RF, Monteiro A. 2005. Process of purification of cashew nut shell liquid (cnsl) for isolation of cardanol. CTF, 2nd Mercosur Congress on Chemical Engineering, Brazil. [Google Scholar]
- Carrier M, Loppinet-Serani A, Denux D, et al. 2011. Thermogravimetric analysis as a new method to determine the lignocellulosic composition of biomass. Biomass Bioenergy 35: 298–307. [CrossRef] [Google Scholar]
- Chrysanthos M, Galy J, Pascault JP. 2011. Preparation and properties of bio-based epoxy networks derived from isosorbide diglycidyl ether. Polymer 52: 3611–3620. [CrossRef] [Google Scholar]
- Darroman E, Bonnot L, Auvergne R, Boutevin B, Caillol S. 2014. New cardanol-based aromatic amines for the synthesis of biobased epoxy networks. Eur. J. Lipid Sci. Technol. 117: 178–189. [CrossRef] [Google Scholar]
- Darroman E, Durand N, Boutevin B, Caillol S. 2015. New cardanol-based aromatic amines for the synthesis of biobased epoxy networks. Prog. Org. Coat. 83: 47–54. [CrossRef] [Google Scholar]
- Darroman E, Durand N, Boutevin B, Caillol S. 2016. Improved Cardanol Derived Epoxy Coatings. Prog. Org. Coat. 91: 9–16. [CrossRef] [Google Scholar]
- Fache M, Darroman M, Besse V, Auvergne R, Caillol S, Boutevin B. 2014. Vanillin, a promising biobased building-block for monomer synthesis. Green Chem. 16: 1987–1998. [CrossRef] [Google Scholar]
- Frank F, Keenan PJ, Plant WJ. 1966. Hydroxy Polyether Polyesters having Terminal Ethylenically Unsaturated Groups. US Patent. [Google Scholar]
- Gandini A. 2011. The irruption of polymers from renewable resources on the scene of macromolecular science and technology. Green Chem. 13: 1061–1083. [CrossRef] [Google Scholar]
- Gaur B, Rai JSP. 1993. Rheological and thermal behaviour of vinyl ester resin. Eur. Polymer J. 29: 1149–1153. [CrossRef] [Google Scholar]
- Greco A, Brunetti D, Renna G, Mele G, Maffezzoli A. 2010. Maffezzoli A.Plasticizer for poly(vinyl chloride) from cardanol as a renewable resource material. Pol. Degrad. Stab. 95: 2169–2174. [CrossRef] [Google Scholar]
- Huong NL, Nieu NH, Tan TTM, Griesser U. 1996. Cardanol-phenol-formaldehyde resins. Thermal analysis and characterization. Ang. Makromol. Chem. 243: 77–85. [CrossRef] [Google Scholar]
- Ionescu M, Petrovic ZSJ. 2011. Phenolation of vegetable oils. Serb. Chem. Soc. 76: 591–606. [CrossRef] [Google Scholar]
- Ionescu M, Wan X, Biliç N, Petrović ZS. 2012. Polyols and rigid polyurethane foams from cashew nut shell liquid. J. Pol. Environ. 20: 647–658. [CrossRef] [Google Scholar]
- Jaillet F, Darroman E, Ratsimihety A, Auvergne R, Boutevin B, Caillol S. 2013. New biobased epoxy materials from cardanol. Eur. J. Lipid Sci. Technol. 116: 63–73. [CrossRef] [Google Scholar]
- Jaillet F, Nouailhas H, Auvergne R, Ratsimihety A, Boutevin B, Caillol S. 2014. Synthesis and characterization of novel vinylesterprepolymers from cardanol. Eur. J. Lipid Sci. Technol. 116: 928–939. [CrossRef] [Google Scholar]
- Jaillet F, Darroman E, Ratsimihety A, Boutevin B, Caillol S. 2015. Synthesis of cardanol oil building blocks for polymer synthesis. Green Materials 3: 1–29. [CrossRef] [Google Scholar]
- Jaillet F, Nouailhas H, Boutevin B, Caillol S. 2016. 39. Synthesis and characterization of novel vinylesterprepolymers from cardanol. EJLST, in press. [Google Scholar]
- Jeong J, Kim B, Shin S, et al. 2013. Synthesis and photo-polymerization of bio-based furanic compounds functionalized by 2-hydroxypropyl methacrylate group(s). J. Appl. Polymer Sci. 127: 2483–2489. [CrossRef] [Google Scholar]
- Kanehashi S, Yokoyama K, Masuda R, Kidesaki T, Nagai Kazukiyo,Miyakoshi T. 2013. Preparation and characterization of cardanol-based epoxy resin for coating at room temperature curing. J. Appl. Pol. Sci. 130: 2468–2478. [CrossRef] [Google Scholar]
- Kim YH, Won K, Kwon JM, et al. 2005. Synthesis of polycardanol from a renewable resources using a fungal peroxidase from Coprinuscireneus. J. Macromol. Cat. B 34: 33–38. [CrossRef] [Google Scholar]
- Kim YH, An ES, Park SY, Song BK. 2007. Enzymatic epoxidation and curing of epoxide-containing polycardanol. J. Macromol. Cat. B 45: 39–44. [CrossRef] [Google Scholar]
- Koike T. 2012. Progress in development of epoxy resin systems based on wood biomass in Japan. Polym. Eng. Sci. 52: 701–717. [CrossRef] [Google Scholar]
- La Scala JJ, Sands JM, Orlicki JA, Robinette EJ, Palmese GR. 2004. Fatty acid-based monomers as styrene replacements for liquid molding resins. Polymer 45: 7729–7737. [CrossRef] [Google Scholar]
- Lespinasse R, Prouvost B, Stenson P. 2011. Polyester polymer having phenolic functionality and coating compositions formed therefrom. US Patent 0315591. [Google Scholar]
- Lukaszczyk J, Janicki B, Frick A. 2012. Investigation on synthesis and properties of isosorbide based bis-GMA analogue. J. Mater. Sci.-Mater. Med. 23: 1149–1155. [CrossRef] [Google Scholar]
- More AS, Pasale SK, Honkhambe PN, Wadgaonkar PP. 2001. Synthesis and characterization of organo-soluble poly(ether ether ketone)s and poly(ether ether ketone ketone) s containing pendant pentadecyl chains. J. Appl. Pol. Sci. 121: 3689–3695. [CrossRef] [Google Scholar]
- O’Connor JC, Chapin RE. 2003. Critical evaluation of observed adverse effects of endocrine active substances on reproduction and development, the immune system, and the nervous system. Pure. Appl. Chem. 75: 2099–2123. [Google Scholar]
- Okada H, Tokunaga T, Liu X, Takayanagi S, Matsushima A, Shimohigashi Y. 2008. Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma. Environ. Health Persp. 116: 32–38. [CrossRef] [PubMed] [Google Scholar]
- Patel MB, Patel RG, Patel VS. 1989. Effects of reactive diluent diepoxidizedcardanol and epoxy fortifier on curing kinetics of epoxyresin. J. Therm. Anal. 35: 47–57. [CrossRef] [Google Scholar]
- Phani Kumar P, Paramashivappa R, Vithayathil PJ, Subba Rao PV, Srinivasa R. 2002. Process for isolation of cardanol from technical cashew (Anacardiumoccidentale L.) nut shell liquid. J. Agric. Food Chem. 50: 4705–4708. [CrossRef] [PubMed] [Google Scholar]
- Pillai CKS, Prasad VS, Sudha JD, Bera SC, Menon ARR. 1990. Polymeric resins from renewable resources. II. Synthesis and characterization of flame-retardant prepolymers from cardanol. J. Appl. Pol. Sci. 41: 2487. [CrossRef] [Google Scholar]
- Sadler JM, Nguyen APT, Toulan FR, et al. 2013. Isosorbide-methacrylate as a bio-based low viscosity resin for high performance thermosetting applications. J. Mater. Chem. A 1: 12579–12586. [CrossRef] [Google Scholar]
- Sato K, Aoki M, Ogawa M, Hashimoto T, Noyori R. 1996. A practical method for epoxidation of terminal olefins with 30 hydrogen peroxide under halide-free conditions. J. Org. Chem. 61: 8310–8311. [CrossRef] [PubMed] [Google Scholar]
- Shen L, Haufe J, Patel MK. 2009. Product overview and market projection of emerging bio-based plastics, Utrecht University commissioned by European Polysaccharide network of excellence and European bioplastics. [Google Scholar]
- Sudhakar MA, Wadgaonkar PP. 2009. Bisphenol compound and process for preparation thereof. US Patent 2009076314. [Google Scholar]
- Sultania M, Rai JSP, Srivastava D. 2010. Studies on the synthesis and curing of epoxidizednovolac vinyl ester resin from renewable resource material. Eur. Pol. J. 46: 2019–2032. [CrossRef] [Google Scholar]
- Sultania M, Rai JSP, Srivastava D. 2011. Process modeling, optimization and analysis of esterification reaction of cashew nut shell liquid (CNSL)-derived epoxy resin using response surface methodology. J. Hazard. Mater. 185: 1198–1204. [CrossRef] [PubMed] [Google Scholar]
- Suresh KI. 2013. Rigid polyurethane foams from cardanol: synthesis, structural characterization, and evaluation of polyol and foam properties. ACS Sustain. Chem. Eng. 1: 232–242. [CrossRef] [Google Scholar]
- Suresh KI, Kishanprasad VS. 2005. Synthesis, structure, and properties of novel polyols from cardanol and developed polyurethanes. Ind. Eng. Chem. Res. 44: 4504–4512. [CrossRef] [Google Scholar]
- Tan TTM. 1996. Cardanol-lignin-based epoxy resins: synthesis and characterization. J. Polymer Mater. 13: 195–199. [Google Scholar]
- Tuck CO, Perez E, Horvath I, Sheldon RA, Poliakoff M. 2012. Valorization of biomass: deriving more value from waste. Science 337: 695–699. [CrossRef] [PubMed] [Google Scholar]
- Tyman JHP. 1975. Long-chain phenols : IV. Quantitative determination of the olefinic composition of the component phenols in cashew nut-shell liquid. J. Chromatgraphy 111: 277–284. [CrossRef] [Google Scholar]
- Unnikrishnan KP, Thomas Thachil EBY. 2008. Studies on the Modification of Commercial Epoxy Resin using Cardanol-based Phenolic Resins. J. Elastomers and Plastics 40: 271–286. [CrossRef] [Google Scholar]
- Verneker SP. 1980. Ind. J. Tech. 18: 170. [Google Scholar]
- Voirin C, Caillol S, Sadavarte NV, Tawade BV, Boutevin B, Wadgaonkar PP. 2014. Functionalization of cardanol: towards biobased polymers and additives. Polymer Chemistry 5: 3142–3162. [CrossRef] [Google Scholar]
- Vom Saal FS, Hughes C. 2005. An extensive new literature concerning low-dose effects of bisphenol A shows the need for a new risk assessment. Environ. Health Persp. 113: 926–933. [CrossRef] [Google Scholar]
- Vom Saal FS, Myers JP. 2008. Bisphenol A and risk of metabolic disorders. J. Am. Med. Assn. 300: 1353–1355. [CrossRef] [Google Scholar]
- Yadav R, Srivastava D. 2009. Synthesis and properties of cardanol-based epoxidizednovolac resins modified with carboxyl-terminated butadiene–acrylonitrile copolymer. J. Appl. Pol. Sci. 114: 1670–1681. [CrossRef] [Google Scholar]
- Yan J, Webster D. 2014. Thermosets from highly functional methacrylatedepoxidized sucrose soyate. Green Mater. 2: 132–143. [CrossRef] [Google Scholar]
Cite this article as: Fanny Jaillet, Emilie Darroman, Bernard Boutevin, Sylvain Caillol. A chemical platform approach on cardanol oil: from the synthesis of building blocks to polymer synthesis. OCL 2016, 23(5) D511.
Different molecules of CNSL, mono-olefinic (8), di-olefinic (8,11), and tri-olefinic (8,11,14).
|In the text|
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.