| 1. |
- Christophliemk, Hanna, 1973-, et al.
(författare)
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Oxygen and water vapor transmission rates of starch-poly(vinyl alcohol) barrier coatings for flexible packaging paper
- 2017
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Ingår i: Progress in organic coatings. - : Elsevier. - 0300-9440 .- 1873-331X. ; 113, s. 218-224
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Tidskriftsartikel (refereegranskat)abstract
- Creating efficient water-borne dispersions based mainly on renewable materials for coating of flexible packaging paper was the aim of this study. The effects of an ethylene modified poly(vinyl alcohol) grade and a standard poly(vinyl alcohol) on the oxygen and water vapor barrier performance of corn starch and potato starch coatings was studied. The results showed that a coating composition with a high fraction of a renewable polymer was effective in keeping the oxygen barrier at a technically and commercially applicable level. An ethylene modified poly(vinyl alcohol) grade was found to provide lower oxygen transmission rates at high relative humidity, as compared to a standard poly(vinyl alcohol) grade. The oxygen barrier properties of blends of starch and poly (vinyl alcohol) were similar to that of the pure modified poly(vinyl alcohol) in the range from 0% starch to 60% starch. This was observed with both hydroxypropylated and octenyl succinate modified starch grades. The drying conditions of the mixed starch:poly(vinyl alcohol) coatings were based on drying trials with pure poly (vinyl alcohol) coatings. Drying at moderate temperatures indicated the possibility to slightly decrease water vapor transmission rate by higher drying temperature. Several secondary effects of increased drying temperature such as coating hold-out and formation of defects may also be of importance.
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| 2. |
- Christophliemk, Hanna, 1973-, et al.
(författare)
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Starch-poly(vinyl alcohol) barrier coatings for flexible packaging paper and their effects of phase interactions
- 2017
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Ingår i: Progress in organic coatings. - : Elsevier. - 0300-9440 .- 1873-331X. ; 111, s. 13-22
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Tidskriftsartikel (refereegranskat)abstract
- Starch and poly(vinyl alcohol) based barrier coatings for flexible packaging papers were studied. Both octenyl succinate modified and hydroxypropylated corn and potato starches were blended with regular and ethylene modified poly(vinyl alcohol) to increase the water vapor barrier properties and enhance the flexibility of the starch coatings, in order to accomplish superior barrier performance. Phase separation between starch and poly (vinyl alcohol) was studied in detail, both in the solution and in dry draw-down coatings on paper. The barrier performance of the coated paper was evaluated with respect to water vapor transmission rate. Conditions for the creation of a thin surface layer consisting of only one of the pure polymers were identified and discussed in terms of phase separation in solution migration of poly(vinyl alcohol) to the uppermost surface layer. The phase separation promoted low water vapor transmission rates also with a rather high fraction of starch in the coatings
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| 3. |
- Hedenqvist, Mikael S., et al.
(författare)
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Extrusion of protein plastics
- 2017
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Ingår i: Abstracts of Papers of the American Chemical Society. - : American Chemical Society (ACS). - 0065-7727. ; 253
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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| 4. |
- Javed, Asif, 1982-, et al.
(författare)
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Crack analysis of barrier coatings based on starch and starch-PVOH with and without plasticizer
- 2018
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 33:2, s. 336-347
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Tidskriftsartikel (refereegranskat)abstract
- Barrier coatings based on starch and starch-PVOH plasticized with glycerol and without plasticizer were applied to two different paperboard substrates, a triple coated board and duplex board, in order to investigate the tendency for cracks to develop in the barrier coating layers during creasing and folding. Tensile properties of films based on the starch and starch-PVOH blend were determined to investigate the relationship between the flexibility of the films and the cracking in the barrier coating layers. Furthermore, the oxygen transmission rate through the barrier-coated paperboard was measured before and after creasing and folding. The oxygen transmission rate through the barrier-coated samples was over the measurable range i. e. OTR > 10000 cm 3 / m 2 day\text{OTR}>10000\hspace{0.1667em}{\text{cm}}^{3}/{\text{m}}^{2}\hspace{0.1667em}\text{day} after creasing and folding, which indicated failure in the barrier coating layers. Optical microscopy revealed small cracks in the barrier coating layers, probably related to an increase in flexibility of the barrier coating layers. It was observed in scanning electron micrographs that cracks in the barrier coating layers seemed to follow the fibers when the barrier coating was applied on the rear side of the duplex board. Scanning electron micrographs and surface profiler images revealed that cracks in the barrier coating layers might have originated from the mineral coating layer when the starch and starch/PVOH coating layers were applied on the mineral-coated side of the triple coated board. An increase in the thickness of the barrier coating layer did not seem to increase the resistance to failure.
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| 5. |
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| 6. |
- Javed, Asif, 1982-, et al.
(författare)
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Lignin-containing coatings for packaging materials
- 2018
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 33:3, s. 548-556
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Tidskriftsartikel (refereegranskat)abstract
- The mechanical properties and chemical stability in water of self-supporting films made from aqueous solutions of starch and lignin, and the barrier properties of paperboard coated with solutions of these polymers have been studied. The dissolution of starch from the starch-lignin films in contact with the model liquids was decreased significantly when lignin was added to the starch films. The addition of ammonium zirconium carbonate (AZC) to the formulations as a crosslinking agent substantially increased the storage modulus of the starch-lignin films, which indicated that crosslinking had occurred. The addition of AZC to the formulations also led to a decrease in dissolution of both starch and lignin from the starch-lignin films in contact with model liquids. The effect of AZC on the water stability of the films was greater when the pH of the starch-lignin-AZC solution was adjusted with ammonia rather than NaOH. The addition of NH4Cl solution as a presumed catalyst to the recipe when the pH adjustment was performed with NaOH did not improve the effect of AZC on the water stability of the films. The water vapour transmission rate of the coated paperboard decreased slightly when AZC was added to the coating formulation.
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| 7. |
- Javed, Asif, 1982-, et al.
(författare)
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Lignin-containing coatings for packaging materials—pilot trials
- 2021
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Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 13:10
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Tidskriftsartikel (refereegranskat)abstract
- One severe weakness of most biopolymers, in terms of their use as packaging materials, is their relatively high solubility in water. The addition of kraft lignin to starch coating formulations has been shown to reduce the water solubility of starch in dry coatings. However, lignin may also migrate into aqueous solutions. For this paper, kraft lignin isolated using the LignoBoost process was used in order to examine the effect of pH level on the solubility of lignin with and without ammonium zirconium carbonate (AZC). Machine-glazed (MG) paper was coated in a pilot coating machine, with the moving substrate at high speed, and laboratory-coated samples were used as a reference when measuring defects (number of pinholes). Kraft lignin became soluble in water at lower pH levels when starch was added to the solution, due to the interactions between starch and lignin. This made it possible to lower the pH of the coating solutions, resulting in increased water stability of the dry samples; that is, the migration of lignin to the model liquids decreased when the pH of the coating solutions was reduced. No significant difference was observed in the water vapor transmission rate (WVTR) between high and low pH for the pilot-coated samples. The addition of AZC to the formulation reduced the migration of lignin from the coatings to the model liquids and led to an increase in the water contact angle, but also increased the number of pinholes in the pilot-coated samples. © 2021 by the authors
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| 8. |
- Javed, Asif, 1982-, et al.
(författare)
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Study of starch and starch-PVOH blends and effects of plasticizers on mechanical and barrier properties of coated paperboard
- 2016
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Ingår i: Nordic Pulp & Paper Research Journal. - : Swedish Association of Pulp and Paper Engineers. - 0283-2631 .- 2000-0669. ; 31:3, s. 499-510
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Tidskriftsartikel (refereegranskat)abstract
- The mechanical properties of self-supporting films based on starch-plasticizer and starch-PVOH-plasticizer and the barrier properties of paperboard coated with solutions of these polymers have been studied. The plasticizers used were glycerol, polyethylene glycol and citric acid. It was shown that the addition of a plasticizer and PVOH to starch substantially increases the flexibility of starch films. It was seen that curing the self-supporting films led to a decrease in flexibility. After heat-treatment, a substantial increase in storage modulus was observed only in the starch-PVOH-citric-acid blend films. Tensile tests on the films indicate that citric acid did not cause any noticeable phase separation. Citric acid acted as a compatibilizer for starch-PVOH blends even though a similar enrichment of PVOH at the air-solid interface was observed with both citric acid and polyethylene glycol as plasticizer. The properties of barrier coatings greatly reflected the compatibility of starch-PVOH blends containing citric acid. The only plasticizer that resulted in a lower water vapour transmission rate through the starch and starch-PVOH coatings was citric acid, which suggests that cross-linking took place. With four layers, coatings based of starch-PVOH possessed the same oxygen- transmission rate with citric acid as without citric acid.
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| 9. |
- Kudahettige-Nilsson, Rasika Lasanthi, et al.
(författare)
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Plastic Composites Made from Glycerol, Citric Acid, and Forest Components
- 2018
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Ingår i: BioResources. - : North Carolina State University. - 1930-2126. ; 13:3, s. 6600-6612
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Tidskriftsartikel (refereegranskat)abstract
- An ecofriendly approach for the synthesis of plastic biomaterials based on renewable materials suitable for 3D printing application or other applications has been developed. The material was prepared from native (microcrystalline) or amorphous cellulose, citric acid, and glycerol or ethylene glycol, by a pretreatment at 40 degrees C and a curing at 175 degrees C for 1 h. The results showed that tensile properties and the water absorption level of the material were acceptable. The highest strain at break (14%) was obtained from materials made of 10% amorphous cellulose with 90% glycerol/citric acid. It had a maximum stress at 37 MPa. Moreover, materials were without ash content. Possible applications of the material in 3D-printers were discussed. In addition, application of mechanical pulp and wood powder into novel plastic material production was discussed. Foaming during curing might be a problem for this type of material, but this can be avoided by using amorphous cellulose in the recipe.
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| 10. |
- Petkova-Olsson, Yana, et al.
(författare)
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Structural, microrheological and kinetic properties of a ternary silica-Pluronic F127-starch thermosensitive system
- 2018
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier. - 0021-9797 .- 1095-7103. ; 514, s. 459-467
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Tidskriftsartikel (refereegranskat)abstract
- Hypothesis: The sol-gel transition in aqueous suspensions consisting of silica particles and thermosensitive polymer is controlled by inter-particle forces and solution properties of the polymer. Addition of a second non-thermosensitive polymer may affect the transition. The purpose of this work was to characterize the kinetics of the sol-gel transition and to understand the effects of a second non-thermosensitive polymer on the microstructure, using a combination of classical rheology and microrheology. Experiments: Classical rotational rheology as well as two microrheology methods, Multiple Particle Tracking (MPT) and Diffusing Wave Spectroscopy (DWS), were used to investigate the sol-gel transition of a ternary silica-Pluronic F127-starch thermosensitive system. Findings: Classical rheometry and DWS indicated sol-gel transition temperature similar to 25 degrees C at 1 wt% Pluronic, independently of the concentration of the other components. DWS showed a fast gelation process, less than two minutes for all samples, beside a second slow kinetic process. In the gel state, MPT indicated micro-structural and micro-viscoelastic differences compared to rotational rheology. This was explained by formation of an elastic matrix of silica and polymers in combination with assembly of silica particles in large macroporous agglomerates. Presence of starch led to breakdown of the macro porous network, leaving the homogeneous elastic network left.
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