| 1. |
- Adamus, Grazyna, et al.
(författare)
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MALDI-TOF MS Reveals the Molecular Level Structures of Different Hydrophilic-Hydrophobic Polyether-esters
- 2009
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 10:6, s. 1540-1546
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Tidskriftsartikel (refereegranskat)abstract
- Multi- and triblock copolymers based on 1,5-dioxepan-2-one/epsilon-caprolactone (DXO/CL) were investigated by MALDI-TOF MS to determine the influence of copolymer composition and architecture on the molecular structures at the individual chain level. The copolymer compositions, average block lengths, and molecular weights were determined by H-1 and C-13 NMR and by SEC, respectively. The structures of polyether-ester oligomers (linear, cyclic) as well as the chemical structures of their end groups were established on the basis of their MALDI-TOF mass spectra. The mass spectrum of PDXO homopolymer was relatively simple, however, complex mass spectra were obtained in the case of multi- and triblock copolymers and the mass spectra clearly discerned the molecular level effect of copolymer composition and copolymer type.
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| 2. |
- Adolfsson, Karin, et al.
(författare)
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Cellulose-derived hydrothermally carbonized materials and their emerging applications
- 2020
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Ingår i: Current Opinion in Green and Sustainable Chemistry. - : Elsevier. - 2452-2236. ; 23, s. 18-24
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Tidskriftsartikel (refereegranskat)abstract
- Hydrothermally carbonized cellulose and its further modifications are intriguing materials for a wide range of potential applications. Hydrothermal carbonization is a sustainable process for converting biopolymers or other biomass sources into carbonaceous materials under mild conditions in water and at relatively low temperatures. This review presents the latest progress in modification and utilization of hydrothermally carbonized cellulose and related materials in environmental, biomedical, and energy applications. Further applications presented include evaluation of cellulose-derived carbon spheres or carbon dots as catalysts, antibacterial materials, flame retardants, and functional fillers in bioplastic composites. The wide range of applications highlights the great potential and multifunctionality of hydrothermally carbonized cellulose and its derivatives. The field is expected to further expand and increase in importance as we move toward circular bioeconomy.
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| 3. |
- Adolfsson, Karin H., et al.
(författare)
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Importance of Surface Functionalities for Antibacterial Properties of Carbon Spheres
- 2019
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Ingår i: Advanced Sustainable Systems. - : Wiley. - 2366-7486.
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Tidskriftsartikel (refereegranskat)abstract
- Carbon spheres (CS) are interesting materials for antibacterial applications. Herein, CS are produced by a green process utilizing microwave-assisted hydrothermal treatment of cellulose. The CS are then postmodified in acidic and basic solutions to evaluate the influence of different functionalities on antibacterial properties. CS contain OH/COOH, C Symbol of the Klingon Empire C, and C Symbol of the Klingon Empire O functionalities, while O-CS produced by acid treatment of CS have additional COOH, and NH/NH2 groups, resulting in carbon spheres with negatively and positively charged groups in dispersion. Treatment with base (Na-CS) removes low molecular weight species with oxygen and results in carbon spheres with the highest C/O ratio. CS, O-CS, and Na-CS have nonporous morphology and are in micro/nanometer sizes, although, smaller sized spheres, hollow spheres, and fragments are also attained in the case of O-CS. O-CS show antibacterial activity toward both Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Pseudomonas aeruginosa (P. aeruginosa). The minimum inhibitory concentration is 200 and 400 mu g mL(-1) for S. aureus and P. aeruginosa, respectively, and is achieved only after 3 h of incubation. Neither CS nor Na-CS exhibit antibacterial activity. The antibacterial activity is suggested to originate from electrostatic interactions between O-CS and the bacteria.
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| 4. |
- Adolfsson, Karin H., et al.
(författare)
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In Vivo Versus In Vitro Degradation of a 3D Printed Resorbable Device for Ligation of Vascular Tissue in Horses
- 2021
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Ingår i: Macromolecular Bioscience. - : Wiley. - 1616-5187 .- 1616-5195. ; 21:10
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Tidskriftsartikel (refereegranskat)abstract
- A resorbable 3D printed polydioxanone (PDO) device is manufactured to facilitate ligation of vascular tissue during surgery. The device must provide sufficient mechanical performance throughout the healing period. Therefore, degradation and mechanical performance of the device are investigated as a function of in vivo and in vitro aging. During aging the PDO device released cyclic and linear water-soluble products. In vivo aging resulted in higher relative number of linear oligomers in comparison to in vitro aging. A major loss of mechanical performance is observed after only 10 days in vivo and the Young’s modulus (E) and tensile strength at break (σb) decreased by 28% and 54%, respectively. This is in contrast to in vitro aging, where no loss of mechanical properties is observed during the same period. The in vivo aged devices exhibit clear holes in the matrices after 28 days, while apparent cracks are observed first after 140 days in vitro. These results highlight the sensitivity of the degradation process of resorbable devices with regards to the interactions of the device with the surrounding environment (tissues) and demonstrate the importance of in vivo testing as compliment to in vitro testing before clinical use of devices.
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| 5. |
- Adolfsson, Karin H., et al.
(författare)
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Microwave Assisted Hydrothermal Carbonization and Solid State Postmodification of Carbonized Polypropylene
- 2018
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Ingår i: ACS Sustainable Chemistry and Engineering. - : AMER CHEMICAL SOC. - 2168-0485. ; 6:8, s. 11105-11114
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Tidskriftsartikel (refereegranskat)abstract
- Functional carbon materials produced through a hydrothermal treatment of waste products have gained interest. Particularly, the method is considered more facile and green compared to conventional decomposition methods. Here, we demonstrated an upcycling of polypropylene (PP) waste to carbon materials by a microwave assisted hydro thermal treatment. The solid product obtained from the hydrothermal treatment was analyzed by multiple techniques to reveal the structure and the influence of processing conditions on PP degradation and hydrothermal carbonization. Chemical analyses showed the presence of carbonaceous material independent of acid amount (20 and 30 mL), temperature (210 and 250 degrees C), and time (20-80 min). A complete transformation of PP content to amorphous carbon required 60 min at 250 degrees C. The mass yield of the solid product decreased as a function of harsher processing conditions. At the same time, thermogravimetric analysis illustrated products with increasing thermal stability and a larger amount of remaining residue at 600 degrees C. The solid products consisted of irregular fragments and sheet-like structures. A solid state microwave process in air atmosphere was performed on a product with incomplete carbonization. The modification resulted in a decreased C/O ratio, and TGA analysis in nitrogen showed high thermal stability and degree of carbonization as indicated by the remaining residue of 86.4% at 600 degrees C. The new insights provided on the hydrothermal carbonization, and postmodification in air atmosphere, can catalyze effective handling of plastic waste by enabling transformation of low quality waste into functional carbon materials.
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| 6. |
- Adolfsson, Karin H., et al.
(författare)
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Oxidized Carbonized Cellulose-Coated Filters for Environmental Contaminant Adsorption and Detection
- 2020
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Ingår i: Industrial & Engineering Chemistry Research. - : American Chemical Society (ACS). - 0888-5885 .- 1520-5045. ; 59:30, s. 13578-13587
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Tidskriftsartikel (refereegranskat)abstract
- Cationized cellulose filters with coating of oxidized carbonized cellulose (OCC) were successfully fabricated. The OCC-coated filter was demonstrated as a combined surface for adsorption of environmental contaminants and their detection on the filter by surface-assisted desorption ionization-mass spectrometry (SALDI-MS). The cellulose filters were cationized by utilizing 3-chloro-2-hydroxypropyltrimethylammonium chloride (CHTAC) and sodium hydroxide. It was shown that the degree of substitution increased with the CHTAC feed. OCC, synthesized by hydrothermal carbonization of cellulose with subsequent oxidation and dialysis, was attached onto the cationized filters by electrostatic interactions. The filters adsorbed the model contaminant methylene blue (MB) from aqueous solution, and the MB could subsequently be detected on the filter surfaces by SALDI-MS as [M](+) adduct. The OCC coating further improved the relative peak intensity of [M](+) with little background interferences. This work indicates great potential for the OCC-coated filters as a combined surface for rapid monitoring of environmental contaminants.
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| 7. |
- Adolfsson, Karin H., et al.
(författare)
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Scavenging of DPPH by Persistent Free Radicals in Carbonized Particles
- 2023
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Ingår i: Advanced Sustainable Systems. - : Wiley. - 2366-7486. ; 7:3
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Tidskriftsartikel (refereegranskat)abstract
- Persistent free radicals (PFR) in carbonized particles may play a role in degradation of environmental compounds. The influence of PFR is evaluated in various carbonized particles on their radical scavenging efficiency upon the common radical indicator 2-2-diphenyl-1-picrylhydrazyl (DPPH). Carbonized particles are derived by hydrothermal carbonization of glucose (C-W) or glucose and urea (NC-W) and ionothermal carbonization of glucose and urea ionic liquid (IL) (NC-IL). The carbonized materials contain OH/COOH, C=C, and C-O functionalities. The addition of urea introduces NH/NH2 functionalities. The content of polar surface groups is lower in IL-processed NC-IL. The scavenging ability, measured as DPPH UV–vis absorption decline, increases with concentration and time for all particles, while the efficiency changes are in the order of C-W > NC-W > NC-IL. Electron paramagnetic resonance analysis reveals similar radical concentration in all carbonized materials studied. The difference in efficiency is, thus, not directly related to the PFR concentration but rather to the type of PFR, surface functionalities and/or scavenging mechanism. According to the g-values, radicals in these particles are carbon-centered. The minor variation in g-values suggests interactions between the radicals and their environmental functional groups. This provides insights into the influence of PFR in carbonized materials on their radical scavenging efficiency.
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| 8. |
- Adolfsson, Karin H., et al.
(författare)
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Valorization of cellulose and waste paper to graphene oxide quantum dots
- 2015
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 5:34, s. 26550-26558
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Tidskriftsartikel (refereegranskat)abstract
- Biobased graphene oxide quantum dots (GOQD) were derived from cellulose via carbon nanospheres (CN) as intermediate products. Solid CN were synthesized from cellulose through microwave-assisted hydrothermal degradation of alpha-cellulose with H2SO4 as a catalyst at 160 degrees C. The obtained CN were further utilized for the synthesis of GOQD by a two-step reaction including 30 minutes of sonication followed by heating at 90 degrees C under O-rich acidic conditions (HNO3). This process broke down the 3D CN to 2D GOQD. The size of the synthesized GOQD was controlled by the heating time, reaching a dot diameter of 3.3 nm and 1.2 nm after 30 and 60 minutes of heating, respectively. The synthesis process and products were characterized by multiple analytical techniques including FTIR, TGA, SEM, TEM, XPS, XRD, BET, DLS and AFM. Interesting optical properties in aqueous solutions were demonstrated by UV/Vis and fluorescence spectroscopy. Finally we demonstrated that corresponding GOQD can be synthesized from waste paper. This production route thus uses renewable and cheap starting materials and relatively mild synthesis procedures leads to instant nanometric production of 2D dots. In addition it enables recycling of low quality waste to value-added products.
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| 9. |
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| 10. |
- Adolfsson, Karin H., et al.
(författare)
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Zero-Dimensional and Highly Oxygenated Graphene Oxide for Multifunctional Poly(lactic acid) Bionanocomposites
- 2016
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Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 4:10, s. 5618-5631
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Tidskriftsartikel (refereegranskat)abstract
- The unique strengths of 2D graphene oxide nanosheets (GONSs) in polymer composites are thwarted by nanosheet agglomeration due to strong intersheet attractions. Here, we reveal that shrinking the planar size to 0D graphene oxide quantum dots (GOQDs), together with the intercalation of rich oxygen functional groups, reduces filler aggregation and enhances interfacial interactions with the host polymer. With poly(lactic acid) (PLA) as a model matrix, atomic force microscopy colloidal probe measurements illustrated that a triple increase in adhesion force to PLA was achieved for GOQDs (234.8 nN) compared to GONSs (80.4 nN), accounting for the excellent exfoliation and dispersion of GOQDs in PLA, in contrast to the notable agglomeration of GONSs. Although present at trace amount (0.05 wt %), GOQDs made a significant contribution to nucleation activity, mechanical strength and ductility, and gas barrier properties of PLA, which contrasted the inferior efficacy of GONSs, accompanied by clear distinction in film transparency (91% and 50%, respectively). Moreover, the GOQDs with higher hydrophilicity accelerated the degradation of PLA by enhancing water erosion, while the GONSs with large sheet surfaces gave a higher hydrolytic resistance. Our findings provide conceptual insights into the importance of the dimensionality and surface chemistry of GO nanostructures in the promising field of bionanocomposites integrating high strength and multifunction (e.g., enhanced transparency, degradation and gas barrier).
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| 11. |
- Adolfsson, Karin
(författare)
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Hydrothermal recycling of natural and synthetic polymers to functional carbon materials
- 2019
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Utilizing renewable recourses and waste recycling are necessary for reaching a circular resource society. The concept of this thesis was to set up a sustainable recycling route, suitable even for low quality biopolymer and plastic waste for production of functional carbon materials. Carbonaceous materials were prepared by mild hydrothermal carbonizations of cellulose and polypropylene (PP) under acidic conditions. The carbonization of cellulose resulted mainly in micro-/nanometer sized carbon spheres (CS) with polar functionalities. After carbonization of PP, products were found in solid and liquid phase. Completely carbonized solid carbons products were obtained from PP at 250 °C after 60 min. The liquid products from the same process displayed aromatics and exhibited fluorescence properties. In addition, new carbon materials were prepared by acid, base and thermal treatments of the carbonized products at low temperatures. Thermally resistant carbon products and antibacterial CS towards both Staphylococcus aureus and Pseudomonas aeruginosa were demonstrated as possible applications for these products. The minimum inhibitory concentrations of CS were 200-400 µg mL-1 depending on the bacteria strain and reached after only 3 h. Furthermore, nanometer sized carbon nanodots with high oxygenation degree and fluorescence properties were derived together with carbon flakes (CF) from the carbonized products. The CF with flat and micrometer sized morphology and polar groups were utilized for coating of cationized cellulose filters, applied as adsorbents and then subsequently as surfaces for SALDI-MS analysis of environmental contaminants. This work contributes with new routes to and applications for functional carbon materials.
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| 12. |
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| 13. |
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| 14. |
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| 15. |
- Albertsson, Ann-Christine, et al.
(författare)
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Emission of volatiles from polymers - A new approach for understanding polymer degradation
- 2006
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Ingår i: Journal of Polymers and the Environment. - : Springer Science and Business Media LLC. - 1566-2543 .- 1572-8919 .- 1572-8900. ; 14:1, s. 8-13
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Tidskriftsartikel (refereegranskat)abstract
- Emission of low molar mass compounds from different polymeric materials was determined and the results from the volatile analysis were applied to predict the degree of degradation and long-term properties, to determine degradation rates and mechanisms, to differentiate between biotic and abiotic degradation and for quality control work. Solid-phase microextraction and solid-phase extraction together with GC-MS were applied to identify and quantify the low molar mass compounds. Volatiles were released and monitored at early stages of degradation before any matrix changes were observed by e.g. SEC, DSC and tensile testing. The analysis of volatiles can thus also be applied to detect small differences between polymeric materials and their susceptibility to degradation. The formation of certain degradation products correlated with the changes taking place in the polymer matrix, these indicator products could, thus, be analysed to rapidly predict the degree of degradation in the polymer matrix and further to predict the long-term properties and remaining lifetime of the product.
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| 16. |
- Albertsson, Ann-Christine, et al.
(författare)
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Molecular weight changes and polymeric matrix changes correlated with the formation of degradation products in biodegraded polyethylene
- 1999
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Ingår i: Journal of environmental polymer degradation. - 1064-7546 .- 1572-8900. ; 64, s. 91-99
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Tidskriftsartikel (refereegranskat)abstract
- The molecular weight changes in abiotically and biotically degraded LDPE and LDPE modified with starch and/or prooxidant were compared with the formation of degradation products, The samples were thermooxidized for 6 days at 100 degrees C to initiate degradation and then either inoculated with Arthobacter paraffineus or kept sterile. After 3.5 years homologous series of mono- and dicarboxylic acids and ketoacids were identified by GC-MS in abiotic samples, while complete disappearance of these acids was observed in biotic environments. The molecular weights of the biotically aged samples were slightly higher than the molecular weights of the corresponding abiotically aged samples, which is exemplified by the increase in (M) over bar(n) from 5200 g/mol for a sterile sample with the highest amount of prooxidant to 6000 g/mol for the corresponding biodegraded sample. The higher molecular weight in the biotic environment is explained by the assimilation of carboxylic acids and low molecular weight polyethylene chains by microorganisms. Assimilation of the low molecular weight products is further confirmed by the absence of carboxylic acids in the biotic samples. Fewer carbonyls and more double bonds were seen by FTIR in the biodegraded samples, which is in agreement with the biodegradation mechanism of polyethylene.
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| 17. |
- Alin, Jonas, et al.
(författare)
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Combined Chromatographic and Mass Spectrometric Toolbox for Fingerprinting Migration from PET Tray during Microwave Heating
- 2013
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Ingår i: Journal of Agricultural and Food Chemistry. - : American Chemical Society (ACS). - 0021-8561 .- 1520-5118. ; 61:6, s. 1405-1415
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Tidskriftsartikel (refereegranskat)abstract
- A combined chromatographic and mass spectrometric toolbox was utilized to determine the interactions between poly(ethylene terephthalate) (PET) food packaging and different food simulants during microwave heating. Overall and specific migration was determined by combining weight loss measurements with gas chromatography-mass spectrometry (GC-MS) and electrospray ionization mass spectrometry (ESI-MS). This allowed mapping of low molecular weight migrants in the molecular range up to 2000 g/mol. Microwave heating caused significantly faster migration of cyclic oligomers into ethanol and isooctane as compared to migration during conventional heating at the same temperature. This effect was more significant at lower temperature at which diffusion rates are generally lower. It was also shown that transesterification took place between PET and ethanol during microwave heating, leading to formation of diethyl terephthalate. The detected migrants included cyclic oligomers from dimer to hexamer, in most cases containing extra ethylene glycol units, and oxidized Irgafos 168. ESI-MS combined with CID MS-MS was an excellent tool for structural interpretation of the nonvolatile compounds migrating to the food simulants. The overall migration was below the overall migration limit of 10 mg/dm(2) set by the European commission after 4 h of microwave heating at 100 degrees C in all studied food simulants.
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| 18. |
- Alin, Jonas, et al.
(författare)
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Microwave heating causes rapid degradation of antioxidants in polypropylene packaging leading to greatly increased specific migration to food simulants as shown by ESI-MS and GC-MS
- 2011
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Ingår i: Journal of Agricultural and Food Chemistry. - : American Chemical Society (ACS). - 0021-8561 .- 1520-5118. ; 59:10, s. 5418-5427
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Tidskriftsartikel (refereegranskat)abstract
- Microwave heating of commercial microwavable polypropylene packaging in contact with fatty food simulants caused significant antioxidant degradation and increased specific migration as shown by electrospray ionization-mass spectrometry (ESI-MS) and gas chromatography-mass spectrometry (GC-MS). Degradation of the antioxidants Irgafos 168 and Irganox 1010 was not detected during conventional heating of polypropylene packaging at the same temperature. The migration into aqueous food simulants was primarily restricted by the water solubility of the migrants. Using isooctane as fatty food simulant caused significant swelling and greatly enhanced overall migration values compared to the other fatty food simulant, 99.9% ethanol, or the aqueous food simulants 10% ethanol, 3% acetic acid, or water. ESI-MS spectra clearly reflected the overall migration values, and the number and amount of compounds detected decreased as the hydrophilicity of the food simulant increased. ESI-MS was shown to be an excellent tool for the analysis of semivolatile migrants and a good complement to GC-MS analysis of volatile migrants.
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| 19. |
- Alin, Jonas
(författare)
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Microwave heating effects on degradation and migration of additives from polypropylene packaging
- 2011
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The effect of different food types, polymer qualities and microwaves on the overall and specific migration during microwave heating of plastic packaging was investigated to better understand the packaging-food interactions and the effect of microwaves on food packaging. This work focuses on the migration of chemical compounds to food simulants from commercially available polypropylene packages. Packages used were made of polypropylene homopolymer (PP), co-polymer (PP-C) and random co-polymer (PP-R). Polymers matrix changes were monitored by following possible changes in crystallinity after microwave heating. Antioxidants Irgafos 168 and Irganox 1010 were present in all the three PP packages. Other volatiles, primarily degradation products of antioxidants, were also detected and identified in the unaged packages. Significant antioxidant degradation took place during microwave heating of the packages in the fatty food simulants 90/10 isooctane/ethanol and ethanol resulting in the formation and migration of degradation products while no degradation of antioxidants was detected during conventional heating of the packages in the fatty food simulants. Antioxidant Irgafos 168 and Irganox 1010 migration rates were otherwise similar during microwave heating as during conventional heating to the fatty food simulants and antioxidant diffusion coefficients were similar to earlier established values obtained during conventional heating. Antioxidant migration rates from the three polymers to fatty food simulants differed largely with respect to PP type and increased with decreasing degree of crystallinity in the materials, PP-R showing the highest migration rate. Swelling in isooctane food simulant caused the antioxidant diffusion coefficients to increase by factors of 100-1000 at 80 ºC and decreased the temperature dependence of antioxidant migration. It also increased the overall migration to above established overall migration limits during both microwave and conventional heating. Electrospray ionization mass spectrometry (ESI-MS) was shown to be a valuable new tool for additive migration analysis of compounds not detectable by HPLC or GC-MS.
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| 20. |
- Alin, Jonas
(författare)
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Migration from plastic food packaging during microwave heating
- 2012
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Microwave heating of food has increased rapidly as a food processing technique. This increases the concern that chemicals could migrate from food packaging to food. The specific effect of microwave heating in contrast to conventional heating on overall and specific migration from common plastic food storage boxes was studied in this work. The purpose was especially to determine the interaction effects of different plastics in contact with different types of foods during microwave heating. The study focused on polycarbonate (PC), poly(ethylene terephthalate) (PET), polypropylene homo-polymer (PP), co-polymer (PP-C) and random co-polymer (PP-R) packages. The migration determinations were evaluated at controlled times and temperatures, using a MAE device. The migrants were analyzed by GC-MS and HPLC. ESI-MS was evaluated as a new tool for migration determinations. Food/food simulant absorption and changes in degree of crystallinity during heating were also followed.Significant degradation of antioxidants Irgafos 168 and Irganox 1010 in PP packages occurred during microwave heating of the packages in food simulants containing ethanol, resulting in the formation of antioxidant degradation products. Degradation of PC by Fries chain rearrangement reaction leading to formation of 9,9-dimethylxanthene, and transesterification of PET leading to formation of diethyl terephthalate, were also observed after microwave heating the packages in ethanol and 90/10 isooctane/ethanol. These reactions were not observed during conventional heating of the packages at the same temperature, or after microwave heating of the packages in liquid food (coconut milk). The microwave heating also significantly increased the migration of cyclic oligomers from PET into ethanol and isooctane at 80 °C. Migration of compounds into coconut milk was slightly lower than calculated amounts using the EU mathematical model to predict migration of additives into foodstuffs. The results thus show that the use of ethanol as a fat food simulant during microwave heating can lead to a significant overestimation of migration as well as degradation of polymer or the incorporated additives.Some other detected migrants were dimethylbenzaldehyde, 4-ethoxy-ethyl benzoate, benzophenone, m-tert-butyl phenol and 1-methylnaphthalene. All identified migrants with associated specific migration limit (SML) values migrated in significantly lower amounts than the SML values during 1 h of microwave heating at 80 °C. The antioxidant diffusion coefficients in PP and PP co-polymers showed larger relative differences than the corresponding degrees of crystallinity in the same polymers and PP-R showed by far the fastest migration of antioxidants.
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| 21. |
- Alin, Jonas, et al.
(författare)
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Migration from polycarbonate packaging to food simulants during microwave heating
- 2012
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Ingår i: Polymer degradation and stability. - : Elsevier BV. - 0141-3910 .- 1873-2321. ; 97:8, s. 1387-1395
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Tidskriftsartikel (refereegranskat)abstract
- The interactions between polycarbonate (PC) packaging and different food simulants during microwave heating were evaluated by identifying the compounds migrating into aqueous, alcoholic and fatty food simulants. The migration of compounds, such as 9,9-dimethylxanthene and m-tert-butyl-phenol, from the PC package to ethanol and isooctane increased significantly during microwave heating as compared to conventional heating. The increase in migration can be explained by degradation caused by microwave heating and/or stronger food simulant interactions. Depending on the food simulant the migrants were quantified either by multiple headspace–solid-phase micro-extraction (MHS-SPME) or direct injection in combination with gas chromatography-mass spectrometry. A partial least squares (PLS) regression model was developed to predict the extraction efficiency for headspace–solid-phase micro-extraction (HS-SPME) of food package migrants from the analyte properties. The most significant property for prediction of the enrichment factors was the octanol-water partition coefficient (log Kow). Polydimethylsiloxane (PDMS) and polydimethylsiloxane/divinylbenzene (PDMS/DVB) fibers were compared for the extraction of the migrants. High correlation was found between the PDMS and PDMS/DVB enrichment factors (R2=0.98), but the extraction by PDMS/DVB fiber was much more efficient compared to the extraction by PDMS fiber. The detection limits after SPME extraction by PDMS/DVB fiber were 1, 0.1 and 3 ng/L for 4-ethoxy-ethyl-benzoate, 2,4-di-tert-butyl-phenol and benzophenone, respectively.
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| 22. |
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| 23. |
- Alin, Jonas, et al.
(författare)
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Type of Polypropylene Material Significantly Influences the Migration of Antioxidants from Polymer Packaging to Food Simulants During Microwave Heating
- 2010
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Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 118:2, s. 1084-1093
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Tidskriftsartikel (refereegranskat)abstract
- Three different polypropylene materials, polypropylene homopolymer (PP), propylene-ethylene random copolymer (PP-R), and propylene-ethylene copolymer (PP-C) are commonly used in plastic containers designed for microwave heating of food. Migration of antioxidants, Irganox 1010 and Irgafos 168, from PP. PP-R, and PP-C during microwave heating in contact with different food simulants was investigated by utilizing microwave assisted extraction (MAE) and high performance liquid chromatography (HPLC). The polypropylene material significantly influenced the migration rate, which decreased in the order of increasing degree of crystallinity in the materials. PP homopolymer was the most migration resistant of the studied materials especially in contact with fatty food simulants. The use of isooctane as fatty food simulant resulted in rapid depletion of antioxidants, while migration to another fatty food simulant, 96% ethanol, was much more limited. Migration to aqueous and acidic food simulants was in most cases under the detection limits irrespective of microwaving time and temperature. The diffusion coefficients were similar to what have been found previously under similar conditions but without microwaves. The effect of swelling was shown by the large increase in the calculated diffusion coefficients when isooctane was used as food simulant instead of 96% ethanol. (C) 2010 Wiley Periodicals, Inc. I Appl Polym Sci 118: 1084-1093,2010
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| 24. |
- Alongi, Jenny, et al.
(författare)
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Superior flame retardancy of cotton by synergetic effect of cellulose-derived nano-graphene oxide carbon dots and disulphide-containing polyamidoamines
- 2019
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Ingår i: Polymer degradation and stability. - : Elsevier. - 0141-3910 .- 1873-2321. ; 169
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Tidskriftsartikel (refereegranskat)abstract
- Linear polyamidoamines containing disulphide groups (SS-PAAs) were prepared by polyaddition of L-cystine with 2,2-bisacrylamidoacetic acid (B-CYSS), N,N'-methylenebisacrylamide (M-CYSS) and 1,4-bisacryloylpiperazine (BP-CYSS). They were evaluated as flame retardants for cotton, alone or with cellulose-derived nano-graphene oxide (nGO) carbon dots, to assess whether, due to their potential as radical scavengers, the latter would improve the already good performance of SS-PAAs. In vertical flame spread tests (VEST), cotton treated with 1% nGO burned as quickly as cotton, whereas B-CYSS, M-CYSS and BP-CYSS extinguished the flame at add-ons >= 12, 16 and 20%, respectively. Probably, the gaseous products of SS-PAA thermal degradation quenched the radicals involved in oxidation. Cotton treated with 8,12 and 15%, respectively, of B-CYSS, M-CYSS and BP-CYSS burned completely, but further addition of 1% nGO either inhibited ignition or shortly extinguished the flame, demonstrating synergism between the two components. Synergism was confirmed by assessing the synergism effectiveness parameter for the residual mass fraction (RMF) and by comparing the calculated and experimental TG curves in air for the cotton/SS-PAA-nGO systems. In cone calorimetry tests, the presence of nGO did not improve the already good performances of SS-PAAs, supporting the hypothesis that the action of both takes place in the gas phase.
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| 25. |
- Aminlashgari, Nina, et al.
(författare)
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Characterization of degradation fragments released by arc-induced ablation of polymers in air
- 2016
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Ingår i: Journal of Physics D. - : Institute of Physics Publishing (IOPP). - 0022-3727 .- 1361-6463. ; 49:5
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Tidskriftsartikel (refereegranskat)abstract
- Polymers exposed to high intensity arc plasmas release material in a process called arc-induced ablation. In order to investigate the degradation fragments released due to this process, two different polymeric materials, poly(oxymethylene) copolymer (POM-C) and poly(methyl methacrylate) (PMMA), were exposed to a transient, high-power arc plasma in air. A small fraction of the ablated material drifting away from the arcing volume was deposited on a fixed glass substrate during the total duration of a 2 kA ac current semicycle. In addition, another fraction of the released material was deposited on a second moving substrate to obtain a time-resolved streak 'image' of the arc-induced ablation process. For the first time, mass spectra of degradation fragments produced by arc-induced ablation were obtained from the material deposited on the substrates by using laser desorption ionization time-of-flight mass spectrometry (LDI-ToF-MS). It was found that oligomers with mean molecular weight ranging between 400 and 600 Da were released from the surface of the studied polymers. The obtained spectra suggest that the detected degradation fragments of POM could be released by random chain scission of the polymer backbone. In turn, random chain scission and splitting-off the side groups are suggested as the main chemical mechanism leading to the release of PMMA fragments under arc-induced ablation.
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