Patent Application
20250066545
The present disclosure relates generally to polymer chemistry and particularly to the syntheses of novel sulfur-bridged difuran polyesters. In certain aspects, the present disclosure also relates to food and beverage packaging materials and curable resins.
Recently, there has been an increased focus on obtaining polymeric materials derived from renewable resources. This growing trend is aiming at finding replacements to fossil-based resources and materials such as poly(ethylene terephthalate), PET, a high performance plastic that is especially widely used in packaging due to its gas barrier properties, transparency, and mechanical strength.
There has been growing interest towards the utilization of renewable lignocellulose-based feedstocks in the production of biobased chemicals and materials. One of the most attractive biochemicals is furfural, a dehydration product of hemicellulose-based C5 sugars. Furfural contains an aldehyde group and the aromatic five-atom furan ring. The single ring substituent of furfural has restricted its utilization in the production of many polymers since two polymerizable groups are often required (e.g., two carboxylic acid functionalities).
2,2′-Bifuran-5,5′-dicarboxylic acid (BFDCA) is one state-of-the-art, furfural-derived dicarboxylic acid which can be used as a monomer in the production of e.g., polyesters with properties such as high gas barrier and intrinsic UV-screening (Kainulainen et al., 2018 and 2020 and Ahmed et al., 2021). To prepare BFDCA, two furfural-derived molecules are connected using a palladium catalyzed coupling reaction, which forms a new C—C bond between the two furan rings. Effective methods that accomplish this are direct coupling (Kainulainen et al., 2018) and reductive homocoupling (Lei et al., 2020).
In this invention, furfural-derived molecules are connected with a sulfur bridge to create a series of novel bifunctional monomers. Notably, the sulfur-bridged monomers are synthesized without expensive transition metal catalysts and the method allows straightforward utilization of furfural as a raw material.
The present invention provides novel furfural-derived bifunctional compounds. The sulfur-containing furan polyesters of the invention are excellent barrier materials and provide some degree of screening in the UV-A region. The novel monomers can be utilized for example in the production of sustainable bioplastics, both thermoplastic polyesters and curable thermosets.
Accordingly, the present invention provides a sulfur-bridged difuran polyester comprising a dicarboxylate component and a diol component, wherein the dicarboxylate component and/or the diol component comprise(s) a sulfur-bridged difuran structure.
In certain aspects, the present invention provides a package or packaging material comprising said polymer.
In certain aspects, the present invention provides a film, yarn fiber or coating comprising or consisting of said polymer.
In other related aspects, the present invention provides a method for preparing a sulfur-bridged difuran, the method comprising the steps of:
In other related aspects, the present invention provides a method for preparing a sulfur-bridged difuran, the method comprising the steps of:
In other aspects, the present invention provides a sulfur-bridged difuran compound comprising or consisting of a structure of any of the following formulas:
In certain aspects, the present invention is directed to the use of the sulfur-bridged difuran compound in preparation of polyester with improved oxygen barrier and/or ultraviolet light (UV) blocking properties compared to poly(ethylene terephthalate) based polymers.
In certain aspects, the present invention provides a curable resin composition comprising at least one of the following sulfur-bridged difuran compounds:
In certain aspects, the present invention is directed to a method for preparing a sulfur-bridged difuran diol comprising the step of reacting the sulfur-bridged difuran aldehyde or ester according to Formula
More specifically, the invention is mainly characterized by what is stated in the independent claims.
As used herein, the term “polymer” describes an organic substance composed of a plurality of repeating structural units (backbone units) covalently connected to one another. The term “polymer” as used herein encompasses organic and inorganic polymers and further encompasses one or more of a homopolymer, a copolymer or a mixture thereof (a blend). The term “homopolymer” as used herein describes a polymer that is made up of one type of monomeric units and hence is composed of homogenic backbone units. The term “copolymer” as used herein describes a polymer that is made up of more than one type of monomeric units and hence is composed of heterogenic backbone units. The heterogenic backbone units can differ from one another by the pendant groups thereof.
The term “polyester” as used herein is inclusive of polymers prepared from multiple monomers that are referred to herein as copolyesters. Terms such as “polymer” and “polyester” are used herein in a broad sense to refer to materials characterized by repeating moieties or units. The polyesters as described herein may have desirable physical and thermal properties and can be used to partially or wholly replace polyesters derived from fossil resources, such as poly(ethylene terephthalate), PET. The term “repeating unit,” as used herein with reference to polyesters refers to an organic structure having a dicarboxylic/dicarboxylate component residue and a diol component residue bonded through an ester linkage.
The term “residue” as used herein, means the organic structure of the monomer in its as-polymerized form as incorporated into a polymer, e.g., through an esterification, transesterification, and/or poly condensation reaction from the corresponding monomer(s). Throughout the specification and claims, reference to the monomer(s) in the polymer is understood to mean the corresponding as-polymerized form or residue of the respective monomer. For purposes herein, it is to be understood that by reference to a copolyester comprising a dicarboxylic/dicarboxylate component and a diol component, the dicarboxylic/dicarboxylate and diol components are present in the polymer in the as-polymerized (as-condensed) form, where it is understood the alkyl ester groups in the starting material are not present in the polyester, except sometimes in end groups of the polyester.
Unless otherwise clear from context, percentages referred to herein are expressed as percent by weight based on the total composition weight.
Unless otherwise stated, properties that have been experimentally measured or determined herein have been measured or determined at room temperature. Unless otherwise indicated, room temperature is 25° C.
Unless otherwise stated, properties that have been experimentally measured or determined herein have been measured or determined at atmospheric pressure.
As used herein, the term “glass transition temperature (Tg)” refers to a temperature range where a polymer changes from a hard, rigid or “glassy” state to a more pliable, compliant or “rubbery” state.
It must also be noted that, as used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless otherwise specified.
The present invention is directed to a sulfur-bridged difuran polyester comprising a dicarboxylate component and a diol component, wherein the dicarboxylate component and/or the diol component comprise(s) a sulfur-bridged difuran structure, wherein the sulfur atom is attached to the two furan rings of the difuran with covalent sulfur-carbon bonds. Preferably, the said dicarboxylate component is any of the following formulas:
Preferably, the said diol component is any of the following formulas:
In some embodiment, the said polyester is a homopolyester comprising repeating units of one of the structures according to formula
and
In some embodiment, the said polyester is a copolyester and said diol component is an aliphatic, cycloaliphatic or aromatic C1-C8 diol. Preferably, the said aliphatic, cycloaliphatic, or aromatic C1-C8 diol is selected from the group consisting of: ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,4-cyclohexanedimethanol, and isosorbide.
In some embodiments, said polyester is a copolyester further comprising an aliphatic or cycloaliphatic C3-C8 dicarboxylic residue, an aromatic C6-C12 dicarboxylic residue or an aromatic C6-C8 dicarboxylic monomer residue as a repeating unit. Preferably, said aromatic C6-C8 dicarboxylic monomer residue is dimethyl terephthalate (DMT).
In some embodiments, the said copolyester comprises repeating units of at least one of the structures according to formula
and
and
Having similar or better properties compared to PET (see Experimental Section below), a person skilled in the art would understand that the above described polyester can be applied to beverage bottles, food package films and other food package containers, cosmetics packages, detergent and washing agent containers, medicinal substance containers, and yarn fibers.
The present invention is thus also directed to a package or packaging material comprising a sulfur-bridged difuran polyester as defined above. Preferably, said package is a food package or a beverage container.
Further, the present invention is directed to a film, yarn fiber or coating comprising or consisting of the a sulfur-bridged difuran polyester as defined above.
The present invention is also directed to a method for preparing a sulfur-bridged difuran, the method comprising the steps of:
Preferably, the method comprises the steps of:
In another preferred embodiment, the method can comprise the steps of:
Alternatively, the method comprises the steps of:
Thus, in a typical procedure sulfur-bridged difuran compounds are synthesized over three reaction steps as presented in
In a preferred embodiment, said sulfur donor in step a) is sodium sulfide (Na2S) or sodium thiosulfate (Na2S2O3).
In some embodiments, the said method further comprises a step of performing a polycondensation process to the compounds produced in step c) in order to produce a polyester.
A typically useful procedure is a conventional two-step melt-polymerization method, such as generally also used in the production of PET. Thereby a mixture of the diol and dicarboxylic monomers are subjected to heating, in two stages. Thus, e.g., the mixture is first exposed to a temperature in the range of 140° C.-220° C., and thereafter to a temperature of 210° C.-260° C. Vacuum may be applied gradually, to obtain high molecular weight polyesters. Typically, the pressure applied during polycondensation step is subatmospheric, for example 0.01 to 900 mBar, for example about 0.1 to 100 mBar.
In preferred embodiments, the compound of
In another preferred embodiment, the compound of
The invention is further directed to sulfur-bridged difuran compounds comprising or consisting of a structure of any of the following formulas:
The present invention is also directed to use of said sulfur-bridged difuran compounds in preparation of polyester with improved oxygen barrier and/or ultraviolet light (UV) blocking properties compared to poly(ethylene terephthalate) based polymers.
The invention further provides a curable resin composition comprising at least one of the following sulfur-bridged difuran compounds:
“Curable” refers to material that is obtained by irreversibly hardening a soft solid or viscous liquid prepolymer by cross-linking of individual chains of the polymeric substance of the resin under the influence of heat or suitable radiation, often under increased pressure. Preferably, the curable composition is cured by heating, or by UV radiation.
The invention is further directed to a composite, an adhesive, or a coating comprising at least one said curable sulfur-bridged difuran compounds.
Composite refers to composite material that comprises at least two components. These components may have notably dissimilar chemical or physical properties and are merged to create a material with properties unlike the individual elements. Within the finished structure, the individual elements remain separate and distinct, distinguishing composites from mixtures and solid solutions.
Adhesive refers to any composition that is capable of holding materials together by surface attachment that resists separation.
It will be obvious to a person skilled in the art that, as the technology advances, the inventive concept can be implemented in various ways. The invention and its embodiments are not limited to the examples described above but may vary within the scope of the claims.
Diols 1,2-ethanediol (99.8%), 1,3-propanediol (98%), and 1,4-butanediol (99%) were either purchased dry or distilled and stored under inert gas prior to use. Glycidol was distilled under reduced pressure prior to use. Otherwise, commercially available chemicals and solvents were used as received. Sodium sulfide hydrate (>60% Na2S) was used as a source of sulfur in the reactions. Tetrabutyl titanate (TBT, 99%) was used as a catalyst for polycondensation reactions. Thin-layer chromatography was used for monitoring reactions using ethyl acetate and hexane (1:1 ratio) as an eluent. The compound numbering 1-9 used below refers to
5,5′-sulfanediyldi(furan-2-carbaldehyde) (1): 5-Bromofurfural (>98%, 10.71 g, 60 mmol) and sodium sulfide hydrate (0.55 equiv, 4.29 g) were reacted in deionized water (200 ml) at 95° C. for 2 hours. The cooled reaction mixture was filtered, and the obtained solid product was dried and purified by filtration through silica layer to afford yellow-orange powder (80%, 5.33 g). Melting point: 130° C. 1H NMR (400 MHZ, CDCl3, ppm): δ 9.62 (s, 2H), 7.25 (d, 2H, J=3.5 Hz), 6.81 (d, 2H, J=3.5 Hz). 13C NMR (100 MHZ, CDCl3, ppm): δ 177.3, 155, 147.8, 121.5, 118.7. HRMS m/z calculated for C10H6O4NaS [M+Na]+: 244.9879, found 244.9877.
5,5′-sulfanediyldi(furan-2-carboxylic acid) (2): Compound 1 (12 g, 54 mmol) and triethylamine (40 mL) were mixed in a 250 mL two-necked flask, equipped with a magnetic stirring bar and a thermometer. The flask was placed in an ice bath, and once the reaction mixture temperature reached 0° C., 30% hydrogen peroxide solution (4 equiv, 22 mL) was added dropwise while keeping the reaction temperature below 20° C. After the addition of H2O2, the reaction flask was removed from the ice bath and the mixture was stirred at room temperature for 2 hours. Excess triethylamine was distilled off under reduced pressure. The reaction mixture was then diluted with 200 mL of deionized water and acidified (pH 1-2) with conc. hydrochloric acid. The formed off-white precipitate was filtered, washed with deionized water, rinsed with ethanol, and dried under vacuum to yield the product (95%, 13.03 g). 1H NMR (400 MHz, DMSO-d6, ppm): δ 13.44 (broad s, 2H), 7.27 (d, 2H, J=3.4 Hz), 7.01 (d, 2H, J=3.4 Hz). 13C NMR (100 MHZ, (CD3)2SO, ppm): δ 159, 148.2, 145.1, 119.7, 119.6. HRMS m/z calculated for C10H7O6S [M+H]+: 254.9957, found 254.9958.
Dimethyl 5,5′-sulfanediyldi(furan-2-carboxylate) (3): Compound 2 (5.08 g, 20 mmol) was mixed with anhydrous methanol (150 mL) and 97% sulfuric acid (2 equiv, 2.23 mL). The mixture was refluxed overnight. The crude product was filtered, washed with cold methanol, and dried under suction to yield yellow crystals (5.4 g). The crude product was purified by sublimating at 170° C. under reduced pressure (<1 mbar), where the product was collected as white crystals in (97%, 5.21 g). Melting point: 153° C. 1H NMR (400 MHZ, CDCl3, ppm): δ 7.17 (d, 2H, J=3.5 Hz), 6.74 (d, 2H, J=3.5 Hz), 3.90 (s, 6H). 13C NMR (100 MHz, CDCl3, ppm): δ 158.3, 147, 146, 119.3, 118.5, 52.2. HRMS m/z calculated for C12H11O6S [M+H]+: 283.0270, found 283.0271.
Diglycidyl ester of 5,5′-sulfanediyldi(furan-2-carboxylic acid) (4): Compound 2 (2.06 g, 8 mmol) and SOCl2 (3 equiv, 1.77 mL) were reacted in refluxing dichloromethane under argon. After overnight refluxing, the solution was filtered and evaporated to yield the crude diacyl chloride (2.29 g, 97%). The diacyl chloride, dissolved in dichloromethane (100 mL) cooled to 0° C. in an ice bath, was mixed with triethylamine (2.25 equiv, 2.77 mL). Under argon, a solution of glycidol in dichloromethane (2.25 equiv, 2.35 mL) was slowly introduced into the mixture over 20 min. Cooling was removed, and the reaction was allowed to continue at room temperature for 1 h. The reaction mixture was then extracted with deionized water, saturated NaHCO3 solution, and brine. The organic layer was dried over anhydrous Na2SO4, filtered through a thin layer of silica gel, and evaporated to dryness to give the product (2.64 g, 92%). Melting point: 70° C. 1H NMR (400 MHZ, CDCl3, ppm): δ 7.20 (d, J=3.4 Hz, 1H), 6.74 (d, J=3.4 Hz, 1H), 4.62 (dd, J=12.2, 3.2 Hz, 1H), 4.14 (dd, J=12.2, 6.4 Hz, 1H), 3.31 (td, J=6.5, 3.1 Hz, 1H), 2.89 (t, J=4.5 Hz, 1H), 2.71 (dd, J=4.9, 2.7 Hz, 1H).
5,5′-Sulfonyldi(furan-2-carboxylic acid) (5): Compound 2 (4.06 g, 16 mmol) was reacted with 30% H2O2 solution (30 mL, 25 equiv) in acetic acid (46 mL) at 85° C. overnight. The reaction mixture was cooled down and filtered, and the solid product dried under vacuum (3.40 g, 74%). 1H NMR (400 MHZ, DMSO-d6, ppm): δ 14.2 (broad s, 2H), 7.43 (d, 2H, J=3.5 Hz), 7.25 (d, 2H, J=3.5 Hz). HRMS m/z calculated for C10H6O8NaS [M+Na]+: 308.9675, found 308.9674.
Dimethyl 5,5′-sulfonyldi(furan-2-carboxylate) (6): Compound 5 (2.86 g, 10 mmol) was mixed with excess of methanol (150 mL) and 97% sulfuric acid (2 equiv, 1.15 mL) and refluxed overnight. The reaction system was allowed to cool down before the product was filtered. The product was recrystallized from methanol and subsequently purified by filtration through a silica layer to afford white crystals (2.93 g, 93%). 1H NMR (400 MHZ, CDCl3, ppm): δ 7.43 (d, 2H, J=3.4 Hz), 7.25 (d, 2H, J=3.4 Hz), 3.92 (s, 6H). HRMS m/z calculated for C12H10O8NaS [M+Na]+: 336.9988, found 336.9977.
Dimethyl 5,5′-sulfinyldi(furan-2-carboxylate) (7): Compound 3 (2.25 g, 8 mmol) was dissolved in CH2Cl2 (40 mL) in 100 mL round flask and cooled down to 0° C. 77% m-CPBA (1.79 g, 8 mmol) in CH2Cl2 (20 mL) was added to the flask dropwise over 30 min. The reaction mixture was stirred for 5 h at −4-0° C. Then, the reaction mixture was extracted twice with 50 mL portions of 10% NaHCO3 solution. The organic phase was dried over MgSO4, filtered, and evaporated to dryness. The mixture was purified through via column chromatography (silica) using hexane and ethyl acetate (1:3) as an eluent to afford the pure sulfoxide as white crystals (1.15 g, 43%). Melting point=118° C. 1H NMR (400 MHZ, CDCl3, ppm): δ 7.27 (d, 2H, J=3.4 Hz), 7.17 (d, 2H, J=3.4 Hz), 3.92 (s, 6H). HRMS m/z calculated for C12H11O7S [M+H]+: 299.0219, found 299.0220.
Polyester synthesis (8a-c): Tetrabutyl titanate (50-400 ppm wt. % relative to monomer weight) was dissolved in dry toluene (0.5 mL) and mixed with the diol (3-5 equiv) along with 3 (2.25 g, 8 mmol) in a 100 mL round-bottom flask equipped with a magnetic stirring bar. The flask was connected to a distillation bridge and the reaction system was evacuated and filled with argon gas 5 times. The transesterification step was started at 180° C. The temperature was raised gradually to 200° C. over 2-4 h until no more methanol was received. For the polycondensation step, the pressure was gradually reduced to 3 mbar over 1 h and the reaction temperature was increased to 230-250° C. Once the excess of diol was distilled off and the pressure reduced to 0.1 mbar, the polymerization was run for 3-5 h. The polymeric product was dissolved in 1,1,1,3,3,3-hexafluoroisopropanol. The addition of methanol precipitated the polyester, which was filtered and washed with cold methanol. The product was dried under vacuum at 65° C. to yield a white-to-off white fibrous polymer. Polyester samples (ca. 10 mg) were dissolved in a mixture of TFA-d and CDCl3 (1:3, v/v) for NMR measurements.
Polyester synthesis (9): Monomer 6 (2.51 g, 8 mmol) was added to a 100 mL reaction flask with TBT (50 ppm wt % equiv), dissolved in 0.5 mL of dry toluene, and mixed with ethylene glycol (2 equiv, 0.89 mL) and Irganox 1010 antioxidant (1000 ppm mol % relative to monomer ratio). The flask was connected to a distillation bridge and the reaction system was evacuated and filled with argon gas 3 times. The monomer was transesterified by ethylene glycol for 2 h at 180° C. and at 200° C. The reaction pressure was decreased gently from 1000 mbar to 3 mbar during 1 h to avoid sublimation of short oligomers. The polymerization step occurred at 250° C. under reduced pressure for 2 h. The crude product was dissolved in 1,1,1,3,3,3-hexafluoroisopropanol then precipitated in cold methanol. The powder was vacuum dried at 60° C. for several days to afford the product (1.7 g, 88%). 1H NMR (400 MHZ, CF3COOD: CDCl31:3, ppm): δ 7.52 (d, 2H, J=3.5 Hz), 7.40 (d, 2H, J=3.5 Hz), 4.76 (s, 4H).
Resin curing experiment: The diepoxy compound 4 was mixed with MHHPA in 1:1 molar ratio. A curing catalyst (0.5 wt %) dissolved in dichloromethane was then added. The mixture was homogenized by heating to 70° C., followed by the application of vacuum (5 mbar) to remove the dichloromethane. The resin was transferred into a silicone mold and cured under reduced pressure in a vacuum oven (at 100, 120, and 150° C., held 2 h at each temperature) to yield a dark solid.
Dilute solution viscometry: Intrinsic viscosities were determined from flow times of pure solvent (phenol: 1,1,2,2-tetrachloroethane 60:40, w/w) (to) and 0.5 g/dL polyester solutions (1) in a micro-Ubbelohde viscometer submerged in 30.0° C. water bath. The average of three flow times were used to calculate t0 and t. Billmeyer equation was used to calculate the intrinsic viscosity according to ASTM D 4603 technique. (Farah et al., 2015)
Differential scanning calorimetry (DSC): Differential scanning calorimeter (Mettler Toledo DSC 821e) was used to investigate thermal behavior of the samples in the range of −10-250° C. under N2 gas flow (50 cm3/min) with heating and cooling rates of 10° C./min. Samples (ca. 2-3 mg) were weighed into a 40 μL Al pans, which were then sealed with pierced lids.
Film processing: Fontijne hydraulic press (LabEcon 300) was used to prepare melt-pressed polymer films. The polyester (1-2 g) was melted between the pre-heated aluminum plates covered with PTFE-coated glass fiber sheets. The thickness was controlled using layers of the same sheet around the sample. The polyesters were melted at 20-30° C. above the expected melting temperatures for 5 minutes, and then pressed for 1 minute at 30 kN. Water-cooling circuit of the press was used to cool the sample.
Tensile testing: Rectangle-shaped specimens with 5 mm width and thicknesses between 100-200 μm were stored for 48 h under stable conditions (23° C., 50% RH) before the tests. Tensile testing (Instron 5544, USA) was performed under the same conditions using a gage length of 30 mm and crosshead speed of 5 mm/min.
Dynamic Mechanical Analysis (DMA): The dynamic mechanical properties of polyesters rectangular melt-pressed film pieces were evaluated using a DMA Q800 (TA Instruments, USA). All runs were performed in a “multi-frequency, strain” mode at 1 Hz, 0.08% strain, from 30 to 150° C. at a heating rate of 3° C./min.
Gas permeability analysis: The oxygen transmission rate (OTR) of the melt-pressed films was measured using a MOCON OxTran 2/20 (23° C. and 0% (relative humidity) with specimen exposure area=5 cm2. OTR values were measured from duplicate samples.
UV-vis: Shimadzu UV-1800 spectrophotometer was used to acquire transmission spectra of films within 200-800 nm.
Dimethyl 5,5′-sulfanediyldi(furan-2-carboxylate)3 was synthesized according to
Other diester monomers, dimethyl 5,5′-sulfonyldi(furan-2-carboxylate) (6) and dimethyl 5,5′-sulfinyldi(furan-2-carboxylate) (7) were received in the following ways. In the presence of H2O2/CH3COOH, the sulfide unit of diacid 2 oxidized affording compound 5 with the desired sulfone unit in good yield. The following esterification of 5 gave the monomer 6 in high 93% yield. Whereas, oxidation of the sulfide unit of 3 with m-CPBA gave the sulfoxide unit bearing monomer 7. In order to demonstrate the utilization of the novel monomers, compound 6 was polymerized with ethylene glycol to receive polyester 9 with intrinsic viscosity of 0.18 dL/g (Table 1).
1H and 13C NMR measurements confirmed the chemical structures. 1H NMR spectra show two sets of duplets in the range of 6.5-7.5 ppm (J=3.5 Hz). These are assigned to the furan ring, while the methylene protons are found at 1.6-4.7 ppm. 13C NMR spectra show the furan ring carbons (114-140 ppm) as well as the carbonyl carbon (156.7 ppm), with the alkyl chain carbons at 20-60 ppm.
The thermal properties of the polyesters are summarized in Table 2. Poly(alkylene sulfanediylbisfuranoate) polyesters showed lower glass transition temperature (Tg) values compared with those corresponding to poly(alkylene furanote) and poly(alkylene bifuranote). PESBF (8a) showed lower Tg (65° C.) than both poly(ethylene furanoate) (87° C., Hong et al., 2016) and poly(ethylene bifuranoate) (107° C., Kainulainen et al., 2018). Also, PBSBF (8c) with the lowest Tg value (37° C.) showed the same trend compared to poly(butylene furanoate) (39° C.) and poly(butylene bifuranoate) (62° C.) (Kainulainen et al., 2020). In contrast to sulfide polyesters, PESO2BF (9) showed high glass transition temperature at 91° C. and melting temperature at 240° C. as sulfone groups give more strength to the polymer chains and restrict their free motion.
The viscoelastic properties of polyesters were analyzed by DMA. Notably, the three parameters storage modulus E′, loss modulus E″ and tan δ for all samples showed the same general variation. It was found that both E″ and tan δ peak temperature values tended to decrease with increasing methylene unit count of the polyesters. The Tg values evaluated from the peak of the E″ curve were in line with those determined by DSC.
Polyesters 8a-c were processed into free-standing films (thickness of 100-200 μm) via melt-pressing. Tensile properties measured from the films (Table 3) fall within the same range as PBF, PEBF, and PBBF (Kainulainen et al., 2018 and 2020).
aAt least five amorphous specimens were evaluated for each polyester composition.
Oxygen permeability coefficients were measured from films for both the polyesters 8a-c and the reference material (PET) for determination of barrier improvement factors (BIFs, Table 4). Polyesters 8a-c showed very high BIFs, which are in the same range as the previously reported values for PEF (Wang et al. 2017). They are higher compared to, e.g., the previously reported values for PBF, PEBF, and PBBF (Kainulainen et al., 2018 and 2020). Therefore, the novel sulfur-containing furan polyesters are excellent barrier materials.
Based on UV-vis transmittance measurements, polyesters 8a-c showed intrinsic UV screening up to ca. 350 nm. PET and FDCA-based polyesters do not provide notable screening in the UV-A region (Kainulainen et al., 2018 and 2020).
Diglycidyl ester 4 was prepared from diacid 2 via conversion into acyl chloride with thionyl chloride in dichloromethane, followed by reaction with glycidol and triethylamine. Diglycidyl ester 4 had a melting point of 70° C. (DSC). 1H NMR spectrum was consistent with the expected product. In one curing experiment, compound 4 was mixed with hexahydromethylphthalic anhydride (MHHPA) in 1:1 molar ratio, with 0.5 wt % imidazole catalyst. The resulting mixture was held under vacuum after transfer into mold and thermally cured at up to 150° C. DSC experiments showed that the resulting fully cured resin had a Tg of ca 120° C.
Furfural can be used as a feedstock for a novel class of polymers, where the key aromatic monomer incorporates a sulfur bridge between two furan rings. In simple linear polyesters, the key monomer structure resulted in amorphous or semi-crystalline polyesters with glass transition temperature ranging from 37-91° C. The tested polyesters had excellent gas barrier properties against oxygen and intrinsic UV block up to about 350 nm.
In anhydride hardened epoxy resins, glass transition temperature of ca. 120° C. was observed. This closely matches the glass transition temperatures attained with diepoxy compounds that are derived from non-renewable terephthalic acid.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20216329 | Dec 2021 | FI | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FI2022/050867 | 12/22/2022 | WO |
