Patent Application
20230026468
The present invention relates to adhesive formulations, in particular pressure sensitive and hot melt adhesive formulations, and composite adhesive formulations for making self-adhesive films. The invention also relates to compostable biopolymer compositions.
Adhesive films are used in a great number of applications and particularly for packaging all sorts of goods. The adhesive industry is continually in search of products with better performance, specific applications and more environment friendly ingredients in the formulations. Adhesives available on the market are non-biodegradable, and petroleum derivatives, thus adversely affecting the environment in both their source and their disposal. A need exists for biodegradable adhesive compositions, biobased adhesive compositions and both biobased and biodegradable adhesive compositions that provide sufficient adhesion for the intended use.
It is an object of the invention to overcome at least one of the above-referenced problems.
The present invention addresses the need for biodegradable/biobased hydrophobic adhesive compositions that provide sufficient adhesion for the intended use, yet degrade later in an environmentally sound fashion, and are produced from renewable sources, thus, being wholly environmental friendly. Broadly, the invention provides for adhesive formulations and adhesive films that comprise medium chain length polyhydroxyalkanoates (hereafter “mcl-PHA”), and in particular non-crystalline mcl-PHA, produced by microbial fermentation of renewable feedstock.
According to a first aspect of the present invention, there is provided an adhesive formulation comprising 5 to 98% (by weight) substantially non-crystalline mcl-PHA.
In one embodiment, the adhesive formulation is selected for uses as a hot melt adhesive (HMA) or a pressure sensitive adhesive (PSA).
In one embodiment, the adhesive formulation comprises a curing (crosslinking) agent. In one embodiment, the curing agent is a peroxide curing agent. In one embodiment, the formulation comprises 0.1% to 5% curing agent. In one embodiment, the formulation comprises 0.5% to 3% curing agent. Preferably, the formulation comprises 3% curing agent. In one embodiment, the curing agent comprises benzoyl peroxide.
In one embodiment, the formulation comprises a nanoclay. Preferably, the formulation comprises from 1% to 3% nanoclay and, suitably, the nanoclay comprises an organo-modified nanoclay.
In one embodiment, the adhesive formulation is a hot melt adhesive, and comprises 25% to 55% mcl-PHA by weight.
In one embodiment, the hot melt adhesive comprises mcl-PHA as a base material, a tackifier, a wax and optionally a filler (i.e. a clay).
In one embodiment, the hot melt adhesive comprises:
In one embodiment, the mcl-PHA has a crystallinity of less than 30%. Preferably, the mcl-PHA has a crystallinity of less than 10%. More preferably, the mcl-PHA has a crystallinity of up to 5%. Most preferably, the mcl-PHA is amorphous.
In one embodiment, the hot melt adhesive comprises:
In one embodiment, the hot melt adhesive comprises:
In one embodiment, the tackifier is biodegradable. In one embodiment, the wax is biodegradable.
In one embodiment, the hot melt adhesive formulation is substantially free of solvent (i.e. less than 5%, 4%, 3%, 2% or 1% solvent).
In one embodiment, the hot melt adhesive formulation comprises a curing agent. Preferably, the formulation comprises from 0.1% to 5% curing agent. Suitably, the formulation comprises 3% curing agent.
Advantageously, the curing agent comprises benzoyl peroxide.
In one embodiment, the hot melt adhesive formulation comprises a nanoclay. Preferably, the hot melt adhesive formulation comprises from 1% to 3% nanoclay. Suitably, the nanoclay comprises an organo-modified nanoclay.
In a preferred embodiment, the hot-melt adhesive formulation is bio-based and/or biodegradable.
The invention also relates to a hot melt adhesive product formed from a hot melt adhesive formulation of the invention. In one embodiment, the HMA product is in the form of a stick.
The invention also relates to formulations useful in making pressure sensitive adhesive layers (hereafter “pressure sensitive adhesive formulations”). The formulations generally include 10-50% mcl-PHA, and preferably about 10-30% mcl-PHA, and high amounts of solvent. The formulations are dried and cured to form the pressure sensitive adhesive layer, and generally is applied to a substrate prior to drying.
In one embodiment, the adhesive formulation is a pressure sensitive adhesive (PSA) formulation. In one embodiment, the pressure sensitive adhesive formulation comprises solvent, mcl-PHA, a peroxide curing agent, and a co-agent, and optionally a filler.
In one embodiment, the PSA formulation comprises a pressure sensitive adhesive formulation comprising 60-85% solvent, 10-30% substantially non-crystalline mcl-PHA, 0.1-5% peroxide curing agent, and 0.01-1% co-agent, and optionally 0.1 to 3.0% filler (i.e. clay).
In one embodiment, the PSA formulation comprises 70-90% solvent, 10-30% substantially non-crystalline mcl-PHA, 0.1-2% peroxide curing agent, and 0.01-1% co-agent, and optionally 0.1 to 3.0% filler (i.e. clay).
Suitably, the mcl-PHA has a crystallinity of less than 30%. Preferably, the mcl-PHA has a crystallinity of less than 10%. More preferably, the mcl-PHA has a crystallinity of up to 5%. Most preferably, the mcl-PHA is amorphous.
The invention also extends to a pressure sensitive adhesive formulation according to any of claims 22 to 25 comprising 65-85% solvent, 10-30% substantially non-crystalline mcl-PHA, 0.1-2% peroxide curing agent, and 0.01-1% co-agent, and optionally 0.1 to 3.0% filler (i.e. clay).
In one embodiment, the PSA formulation comprises 78-82% solvent, 16-22% mcl-PHA, 0.3-0.8% peroxide curing agent, and 0.06-0.15% co-agent, and optionally 0.5 to 1.5% filler (i.e. clay).
In another embodiment, the PSA formulation comprises A pressure sensitive adhesive formulation according to any of claims 22 to 27, and comprising 75-82% solvent, 16-22% substantially non-crystalline mcl-PHA, 0.3-0.8% peroxide curing agent, and 0.06-0.15% co-agent, and optionally 0.5 to 1.5% filler (i.e. clay).
In one embodiment, the peroxide curing agent is selected from benzoyl peroxide, lauroyl peroxide and dicumyl peroxide.
In one embodiment, the co-agent is selected from a multifunctional acrylate and methacrylate ester and dimaleimides. In one embodiment, the multifunctional acrylate is an ethylene glycol dimethacrylate.
In one embodiment, the PSA formulation comprises a nanoclay. Suitably, the formulation comprises from 1% to 3% nanoclay. Preferably, the nanoclay comprises an organo-modified nanoclay.
In a preferred embodiment, the PSA formulation is bio-based and/or biodegradable.
In one embodiment, the solvent is a non-polar solvent such as chloroform or acetone
In one embodiment, the pressure sensitive adhesive formulation is dried and cured to provide a pressure sensitive adhesive layer, the pressure sensitive adhesive layer comprising at least 80% substantially non-crystalline mcl-PHA by weight.
In one embodiment, the pressure sensitive adhesive layer comprises at least 70%, 80% or 90% or 98% substantially non-crystalline mcl-PHA by weight. In one embodiment, the pressure sensitive adhesive layer comprises about 80% to about 90% mcl-PHA. In one embodiment, the pressure sensitive adhesive layer comprises about 82% to about 86% mcl-PHA.
In one embodiment, the pressure sensitive adhesive layer has a thickness of 50-500 μm, typically 60-400 μm, and ideally about 60-300 μm.
The invention also provides a PSA product comprising a PSA layer on a backing substrate. The backing substrate may be a film (i.e. a polymer film such as a PET film), paper, metallic foil or any other suitable substrate, and is generally a planar material. The product may be a film, label, or sticker. The product is generally formed by spreading PSA formulation on the substrate to drying and curing the formulation to provide a PSA layer.
The invention also relates to a method of making a PSA product (of the invention) comprising the steps of dissolving substantially non-crystalline mcl-PHA in a suitable solvent;
adding the peroxide curing agent and co-agent (and optionally a filler) to the dissolved substantially non-crystalline mcl-PHA with stirring to provide a liquid PSA formulation;
applying a layer of the liquid PSA formulation on to a suitable substrate;
allowing the layer of liquid PSA formulation to dry;
and crosslinking the PSA formulation at elevated temperature for a suitable curing period.
In one embodiment, the PSA formulation is dried for at least 4, 8, 12, 18 or 24 hours. This allows sufficient amount of solvent to evaporate to solidify the PSA while allowing it to function as a hot melt pressure sensitive adhesive.
In one embodiment, the PSA formulation is cured at a temperature of 70-150 C, preferably 70-90C, and ideally at about 80 C. In one embodiment, the PSA formulation is cured for 1-10 hours, 2-7 hours, and ideally about 3-5 hours. The time and temperature of curing can be varied to vary the properties of the PSA.
All publications, patents, patent applications and other references mentioned herein are hereby incorporated by reference in their entireties for all purposes as if each individual publication, patent or patent application were specifically and individually indicated to be incorporated by reference and the content thereof recited in full.
Definitions and General Preferences
Where used herein and unless specifically indicated otherwise, the following terms are intended to have the following meanings in addition to any broader (or narrower) meanings the terms might enjoy in the art:
Unless otherwise stated or required by the context, all % values provided herein are weight %.
Unless otherwise required by context, the use herein of the singular is to be read to include the plural and vice versa. The term “a” or “an” used in relation to an entity is to be read to refer to one or more of that entity. As such, the terms “a” (or “an”), “one or more,” and “at least one” are used interchangeably herein.
As used herein, the term “comprise,” or variations thereof such as “comprises” or “comprising,” are to be read to indicate the inclusion of any recited integer (e.g. a feature, element, characteristic, property, method/process step or limitation) or group of integers (e.g. features, element, characteristics, properties, method/process steps or limitations) but not the exclusion of any other integer or group of integers. Thus, as used herein the term “comprising” is inclusive or open-ended and does not exclude additional, unrecited integers or method/process steps.
As used herein, the term “medium chain length polyhydroxyalkanoates” or “mcl-PHA” refers to linear polyesters having an average monomer chain length of C6 to C14, and which are biodegradable. These polyesters are produced by bacterial fermentation of a suitable substrate, typically sugars or lipids. In preferred embodiments, the mcl-PHA is substantially non-crystalline, and typically has a crystallinity of less than 30% as determined by a method of x-ray diffraction. Typically, the substantially non-crystalline mcl-PHA has a crystallinity of less than 30% while in preferred embodiments the mcl-PHA has a crystallinity of less than 10%. Ideally, the substantially non-crystalline mcl-PHA has a crystallinity of up to 5%, preferably from about 2 to 5%. In particularly preferred embodiments, the substantially non-crystalline mcl-PHA is amorphous.
Methods of producing mcl-PHA are described in the literature, including Lee et al (Biotechnology and Bioengineering, Vol. 68, No. 4, 2000), and Madison et al (Microbiology and Molecular Biology Reviews, March 1999, P21-53) in which mcl-PHA is referred to as msc-PHA and formation by Pseudomonas from fatty acids is described on pages 39 and 40.
As used herein, the term “adhesive” refers to a substance that is applied to a surface and binds the surface to a second surface. Various forms of adhesives are known including pressure sensitive adhesives and hot melt adhesives. Adhesives may be provided in different forms, for example adhesives glue which may be solid or liquid, hot melt adhesive which is generally solid at room temperature and which requires heat for delivery/application, and pressure sensitive adhesive which is also generally solid and tacky. Many adhesives are provided in the form of adhesive films (also known as “self-adhesive films”) which are generally produced from adhesive formulations which are hot-pressed/extruded into the form of a film. The adhesives of the invention comprise mcl-PHA, typically in an amount of 5-95%, and are therefore at least partly biodegradable, and in some embodiments comprise at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 98% mcl-PHA (by weight). In some embodiment, the adhesive (i.e. pressure sensitive adhesive or self-adhesive films) are cured, typically with a peroxide curing agent. In some embodiment, the adhesive is a composite adhesive agent and includes mcl-PHA and in addition either a second biodegradable polymer (i.e. polylactic acid) or a non-biodegradable thermoplastic elastomer, for example an acrylate-based thermoplastic elastomer.
As used herein, the term “curing agent” or “crosslinking agent” refers to agents employed to toughen or harden polymers by cross-linking of polymer chains. It is also referred to as a vulcanisation agent. Curing agents are well known to a person skilled in the art of polymer chemistry. Peroxide curing agents are particularly useful for the adhesives of the present invention, and include benzoyl peroxide, dicumyl peroxide, lauryl peroxide, 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane (DTBPH) and Di(tert-butylperoxyisopropyl)benzene (DTBPIP). Suitable peroxide curing (vulcanisation) agents are described in Section 2.1 of Alvarez-grima et al (PhD Thesis, University of Twente, Enschede, Netherlands, 2007 ISBN: 90-365-2456-3).
As used herein, the term “composite adhesive agent” refers to an adhesive comprising a biodegradable agent such as mcl-PHA and a non-biodegradable thermoplastic elastomer. In one embodiment, the composite adhesive agent comprises 5% to 75% mcl-PHA and 25% to 95% non-biodegradable thermoplastic elastomer, and optionally a curing agent. In one embodiment, the invention provides an adhesive film, especially a self-adhesive film, formed obtainable from a composite adhesive agent of the invention. The film is generally obtainable by hot-pressing/extruding the agent to form the film.
As used herein, the term “biodegradable” as applied to an adhesive or material means that the adhesive or material can be degraded by enzymatic processes resulting from the action of enzymes derived from cells degrading it, for example bacterial or fungal cells. Mcl-PHA is a biodegradable material.
As used herein, the term “bio-based” as applied to an adhesive or material means that the adhesive or material is made from resources originating in renewable resources where the carbon is young relative to fossil based resources.
As used herein, the term “thermoplastic elastomer” refers to a polymer having both thermoplastic and elastomeric properties, and generally elastomeric properties during use and thermoplastic properties during melt. Suitable examples for use in the present invention include acrylate-based thermoplastic elastomers described in Dufour et al (Macromolecular Chemistry & Physics, 209, 1686-1693 (2008)), Dufour et al (Macromolecules, 41, 2451-2458 (2008)), Mosnacek et al (Polymer, 50, 2087-2094 (2009)), Nese et al (Macromolecules, 43, 1227-1235 (2010)), and Juhari et al (Polymer, 21, 4806-4813 (2010)). In one embodiment, the thermoplastic elastomer is selected from poly(ethylene-co-methacrylate-co-glycidylmethacrylate) and poly(ethylene-co-ethacrylate-co-maleicanhydride), or derivates thereof having elastomeric properties during use and thermoplastic proterties during melt. In one embodiment, the thermoplastic elastomer is a random terpolymer of ethylene, acrylic ester and glycidyl methacrylate or maleic anhydride.
As used herein, the term “hot-pressing” for forming adhesive film” refers to pressing of the adhesive film under temperature and pressure to produce uniform thickness film.
As used herein, the term “hot melt adhesive” or “HMA” refers to a form of thermoplastic adhesive that is supplied in solid form (generally as a stick) and designed to be melted and applied using a hot glue gun. The adhesive is generally tacky when hot and solidifies in a few seconds to one minute. Hot melt adhesives can also be applied by dipping, coating or spraying. Generally, the HMA comprises mcl-PHA as a base material, a tackifier, a wax and optionally a filler (i.e. a clay). In one embodiment, the tackifier is biodegradable. In one embodiment the wax is biodegradable. In one embodiment, the HMA comprises 25% to 55% mcl-PHA. In one embodiment, the HMA comprises 25% to 40% mcl-PHA. In one embodiment, the HMA comprises 25% to 35% mcl-PHA. In one embodiment, the HMA comprises about 28% to about 30% mcl-PHA. In one embodiment, the HMA comprises 35% to 55% tackifier. In one embodiment, the HMA comprises 40% to 50% tackifier. In one embodiment, the HMA comprises about 42% to about 47% mcl-PHA. In one embodiment, the HMA comprises 2% to 35% wax. In one embodiment, the HMA comprises 10% to 30% wax. In one embodiment, the HMA comprises 15% to 25% wax. In one embodiment, the HMA comprises about 18% to about 22% wax. In one embodiment, the wax is selected from Bees wax, Carnauba wax, and Paraffin wax. In one embodiment, the wax includes a biodegradable wax (i.e. Carnauba wax) and optionally a non-biodegradable wax (i.e. Parafin wax). The HMA may also include one or more addition additives selected from an anti-oxidant, a detackifier, and a plasticizer.
As used herein, the term “wax” refers to a class of organic compounds that are hydrophobic, malleable solids at or near ambient temperature, that are insoluble in water and soluble in organic non-polar solvents, and that generally comprise higher alkanes and lipids with melting points above 40 C. The wax may be a biodegradable wax, for example an animal wax or a plant wax, or a modified version of a plant or animal wax, or a petroleum derived wax. Examples of plant and animal waxes include beeswax, spermaceti, lanolin, carnauba wax, candelila wax and ouricury wax. Examples of petroleum derived waxes include paraffin wax. Paraffin waxes are mixtures of saturated n- and ios- alkanes, naphthenes, and alkyl- and naphthene-substituted aromatic compounds. In one embodiment, the paraffin wax is a low viscosity paraffin wax.
As used herein the term “tackifier” refers to chemical compounds used in formulating adhesives to increase the tack (the skickiness of the surface of the adhesive). They are described in Tse et al (Journal of Adhesion Science and Technology. 3(1): 551-570). In one embodiment, the tackifier is a resin, for example rosins and their derivatives (for example a hydrogenated rosin), terpenes and modified terpenes, aliphatic, cycloaliphatic and aromatic resins, hydrogenated hydrocarbon resins and their mixtures, and terpene phenol resins. In one embodiment, a combination of tachifiers is employed in the HMA. In one embodiment, the tackifier or tackifiers have a softening point greater than 60° C. In one embodiment the tackifier is biodegradable. Examples include esters of hydrogenated rosins (i.e. Foral 85) and polytherpene resin (i.e. Piccolyte F105).
As used herein, the term “filler” refers to a material that adds bulk to the HMA and improves cohesive strength. Examples includes clays such as kaolin, calcium carbonate, barium sulphate, talc, silica, carbon black.
As used herein, the term “plasticizer” refers to an additive used in HMA's that increase the plasticity or viscosity of the HMA. Examples include oils including animal, plant or petroleum based oils, benzoates such as 1-4-cyclohexane dimethanol, phthalates, and chlorinated paraffins. Examples of biodegradable plasticizers include plant and animal oils and acetyl tributyl citrate.
As used herein, the term “pressure sensitive adhesive” refers to an adhesive which forms a bond to a substrate when pressure is applied to marry the adhesive to the substrate. It is used in pressure sensitive tapes, labels, glue dots, note pads, automobile trim and many other products. The invention provides pressure sensitive adhesive formulations, cured pressure sensitive adhesive, and pressure sensitive adhesive products comprising cured pressure sensitive adhesive applied to a substrate such as a film. The formulation comprises mcl-PHA, a peroxide curing agent, optionally a co-agent and in one embodiment a filler. The mcl-PHA is generally dissolved in a suitable solvent (i.e. chloroform) before the curing agent and optional co-agent and filler are added, and the formulation is then generally applied as a film to a substrate, dried and then heat cured.
As used herein “peroxide curing agent” refers to a peroxide compound suitable for vulcanisation of polymers. Peroxide curing agents are well known in the art, and include benzoyl peroxide, dicumyl peroxide, lauryl peroxide, 2,5-Dimethyl-2,5-di(tert-butylperoxy)hexane (DTBPH) and Di(tert-butylperoxyisopropyl)benzene (DTBPIP). Suitable peroxide curing (vulcanisation) agents are described in Section 2.1 of Alvarez-grima et al (PhD Thesis, University of Twente, Enschede, Netherlands, 2007 ISBN: 90-365-2456-3).
As used herein, the term “co-agent” refers to a multifunctional organic compound that is highly reactive towards free-radicals. They are used as reactive additives to boost peroxide vulcanisation efficiency. Generally, the co-agent comprises a molecule with (meth)acrylate groups, maleimide groups, or allylic groups, although polymeric materials with a high vinyl content (i.e. 1,2-polybutadiene) can also act as a co-agent. In one embodiment, the co-agent is a so-called Type I co-agent, which are substantially polar molecules with a low molecular weight and activated double bonds. Examples include maleimide and (meth)acrylate based co-agents, and specific examples include ethylene glycol dimethacrylate (EDMA), N,N-m-phenylenedimaleimide (BMI-MP), and Trimethylolpropane trimethacrylate (TMPTM). Suitable co-agents are described in Section 2.2 of Alvarez-grima et al (PhD Thesis, University of Twente, Enschede, Netherlands, 2007 ISBN: 90-365-2456-3).
The invention will now be described with reference to specific Examples. These are merely exemplary and for illustrative purposes only: they are not intended to be limiting in any way to the scope of the monopoly claimed or to the invention described. These examples constitute the best mode currently contemplated for practicing the invention.
A. Pressure Sensitive and Hot Melt Adhesives based on Bioplastech mcl-PHA: PSA Formulations and Results
The PSA is prepared by a crosslinking reaction of mcl-PHA (O) and di functional acrylic co-monomer (co-agent) using a peroxide as free radical initiator for crosslinking. The chemical structures of the peroxide (benzoyl peroxide) and the difunctional co-agent (ethylene glycol dimethacrylate) are shown in 4. Various other peroxides such as lauroyl peroxide and dicumyl peroxide were also evaluated as free radical initiators for cross linking the mcl-PHA.
Preparation and Evaluation
In a typical process scheme, films are prepared as follows:
The resultant PSA adhesive thickness is in the range of 80-300 μm. 5 shows the dried PSA films on cellulose substrate.
In order to improve the peel strength of PSA films, solutions were also prepared with 1 wt % synthetic nanoclay Somasif MAE. For selected compositions a desired amount of nanoclay was dispersed in chloroform and added to mcl-PHA solution in chloroform [step (i)].
To evaluate the best crosslinking initiator and the extent of cross linking reaction, the amount of gel content was measured in the final films, produced using either benzoyl peroxide, lauroyl peroxide or dicumyl peroxide. Mechanical properties were also tested.
For these evaluations, material was prepared as described above in steps i) and ii), and the solution then pipetted into a Petri dish. The solvent was allowed to evaporate over approximate two days. The polymer films obtained, typically 5 mm thick, were allowed to crosslink in a vacuum oven according to time and temperatures mentioned in 1.
To measure the gel content, a sample of a film is weighed and placed in a round-bottomed flask containing approximately 5-10 ml of chloroform. The film is allowed to sit in the solvent for 2 h at room temperature and is agitated periodically. After 2 hr the film is retrieved by filtering it off chloroform solution and the gel is placed in a glass dish and allowed to dry for 1-3 days until the weight remains constant.
The percentage of solids (% sol) is calculated from Equation 1. Films prepared with Benzoyl peroxide has shown highest % solids which indicate maximum extent of crosslinking compared to other two initiators.
Mechanical Properties
The mechanical properties of crosslinked and nanocomposites PSA films prepared using benzoyl peroxide as crosslinking agent are shown in Table 2.
With increase in benzoyl peroxide content from 1.5 wt % to 4 wt %, tensile strength increases by 255% (from 0.1 MPa to 0.38 MPa), Young's modulus increases by 161% (0.07 to 0.19 MPa). With addition of 1 wt % nanoclay to the sample with 3 wt % benzyl peroxide, tensile strength of the films was further improved by 68%.
Peel Test and Sol-Gel Analysis
Peel adhesion test of the PSA films was performed based in ASTM 3330 (Peel Adhesion of Pressure-Sensitive Tape) using the mcl-PHA crosslinked films with various concentrations of benzoyl peroxide. Peel tests were performed using the coated flexible PET (labels) substrate at 180° angle to the pristine samples without nanoclay. The peel strength of the PSA formulations is presented in Table 3.
Although films with 1 wt % crosslinking agent have higher peel strength, the material integrity and the film uniformity were poor compared to films prepared with 3% crosslinking agent. For all further optimisation PSA films were prepared with 3 wt % benzoyl peroxide.
Shear Test at Low Temperatures
Shear test under low temperature was performed to demonstrate performance at for low temperature environments. EN 1943 (Self Adhesive Tapes—Measurement of Static Shear Adhesion) procedure G (test conducted at elevated temperature) was adapted. This test aims to determine the ability of a PSA to remain adhered under a constant load applied parallel to the surface of the tape and substrate.
Measurements were carried out −16.5° C., −4.0° C. and 18° C. (ambient) temperature. The test mass employed in this test was 1000 g, and the results are shown in Table 4. The films coated with the developed PSA were polyethylene terephthalate (PET) and cellulose films, two different substrates (panels) were tested; a stainless steel (SS) panel and a PET panel. The results show that the performance are highly dependent on choice of substrate and adhered material, in all cases the coated film exhibited bonding abilities at low temperatures moreover for the films against PET substrate which showed to perform significantly better at the lowest temperature. This is desirable result since PET substrate is more likely to be used in the envisioned application.
HMA Formulations and Results
mcl-PHA was combined with biodegradable and non-biodegradable wax, and with other additives such as tackifiers, nanoclays and surfactants to formulate an HMA. Some compositions are biodegradable and other compositions are not 100% biodegradable; all of them are either fully or partially bio-based. The tackifying resins were selected from a group of natural and modified rosins.
Preparation and Evaluation
Hot melt adhesives were prepared using Bioplastech mcl-PHA (PHA12 or O). The schematic of experimental set-up is shown in
Two different formulations, only differing in the type of wax contained, were selected for evaluation against a commercial sample the formulations are presented in Table 5. The resultant adhesive was used to assemble various disposable containers such as boxes and shopping bags.
The optimal composition identified as an HMA contains (weight fractions):
In order to determine the operation window for the mcl-PHA based HMA, the viscosity of the HMA was measured at various temperatures using a Brookfield viscometer DV-II (Spindle CS4) with a Thermosel control system to accurately measure the melt viscosity at elevated temperatures. Two commercially available adhesives were compared with our selected formulation G60 (
The recommended application temperatures correspond to a viscosity between 830-1600 cP, from which we infer that the application temperature for the G60 mcl-PHA adhesive should be between 100 and 120° C.
Hot melt adhesives need to be stable both during storage and processing as well as during application. In particular thermal stability of hot-melt adhesives is of major importance. An increase of viscosity over time at the application temperature would create problems for the end user, leading to (for example) unscheduled interruptions in production because of plugged transfer lines and applicators. An example of an unstable adhesive behaviour is shown in
The thermal stability of the formulation is however expected to be lower than petroleum-based adhesives.
Peel strength is an important parameter which determines the adhesive strength between the two surfaces which determines the suitability adhesive for given application. In order to evaluate the peel strength of the adhesives developed, a laminating film of two PET strips was obtained by placing the adhesive between the PET films using hydraulic press at 130° C.
The peel test was carried out as per ASTM D3330 IS08510, and IS011339. These results are compared with two commercial available adhesives EVA based BAM802 for label applications, and BAM 356A for packaging applications. The formulations prepared with mcl-PHA show better peel strength compared to commercial HMA.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1718470.6 | Nov 2017 | GB | national |
This application is a divisional of U.S. application Ser. No. 16/762,495, filed on Nov. 8, 2018, which is the U.S. National Stage of International Application No. PCT/EP2018/080640, filed on Nov. 8, 2018, which designates the U.S., published in English, and claims priority under 35 U.S.C. § 119 or 365(c) to GB Application No. 1718470.6, filed on Nov. 8, 2017. The entire teachings of the above applications are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16762495 | May 2020 | US |
| Child | 17946166 | US |
