| 1. |
- Liu, X. H., et al.
(författare)
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Polyamide 6/clay nanocomposites using a cointercalation organophilic clay via melt compounding
- 2003
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Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 88:4, s. 953-958
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Tidskriftsartikel (refereegranskat)abstract
- Polyamide 6/clay nanocomposites (PA6CN) were prepared via the melt compounding method by using a new kind of organophilic clay, which was obtained through cointercalation of epoxy resin and quaternary ammonium into Na-montmorillonite. The dispersion effect of this kind of organophilic clay in the matrix was studied by means of X-ray diffraction (XRD) and transmission electron microscopy (TEM); the silicate layers were dispersed homogeneously and nearly exfoliated in the matrix. This was probably the result of the strong interaction between epoxy groups and amide end groups of PA6. The mechanical properties and heat distortion temperature (HDT) of PA6CN increased dramatically. The notched Izod impact strength of PA6CN was 80% higher than that of PA6 when the clay loading was 5 wt%. Even at 10 wt% clay content, the impact strength was still higher than that of PA6. The finely dispersed silicate layers and the strong interaction between silicate layers and matrix decreased the water absorption. At 10 wt% clay content, PA6CN only absorbs half the amount of water compared with PA6. The dynamic mechanical properties of PA6CN were also studied.
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| 2. |
- Liu, X. H., et al.
(författare)
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Polyamide 6-clay nanocompositles/polypropylene-grafted-maleic anhydride alloys
- 2001
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Ingår i: Polymer. - 0032-3861 .- 1873-2291. ; 42:19, s. 8235-8239
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Tidskriftsartikel (refereegranskat)abstract
- Polyamide 6-clay nanocomposites (PA6CN) based on montmorillonite typically show some brittleness with clay addition. In order to address this problem, PA6CN/PP-g-MAH alloys were prepared through blending PA6CN with polypropylene-grafted-maleic anhydride (PP-g-MAH). The mechanical properties, dynamic mechanical temperature spectra, morphology and water absorption of the alloys were studied. Compared with PA6CN, the notched impact strength of the alloys increased greatly while the alloys still maintained higher stiffness and strength than that of PA 6. The morphological studies via scanning electron microscopy (SEM) showed a PP-g-MAH toughen phase dispersed in PA6CN matrix. As the PP-g-MAH content was increased, reduced water absorption was observed.
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| 3. |
- Liu, X. H., et al.
(författare)
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Investigation on unusual crystallization behavior in polyamide 6/montmorillonite nanocomposites
- 2002
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Ingår i: Macromolecular materials and engineering. - 1438-7492 .- 1439-2054. ; 287:8, s. 515-522
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Tidskriftsartikel (refereegranskat)abstract
- The crystallization behavior and crystal structure of polyamide 6/montmorillonite (PA6/MMT) nanocomposites were investigated by differential scanning calorimetry and X-ray diffraction, and an interesting behavior was observed. The material was prepared via melt compounding using an organophilic clay obtained by co-intercalation of epoxy resin and quaternary ammonium into Na-montmorillonite. A maximum in degree of crystallinity was obtained at 5 wt.-% MMT and the reasons for this, based on the MMT layer distribution, were discussed. The degree of crystallinity showed a strong dependence on the cooling rates. In contrast with typical behavior, a higher cooling rate resulted in a higher degree of crystallinity. In nanocomposites, the gamma-crystalline phase was dominant.
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| 4. |
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| 5. |
- Zhang, L., et al.
(författare)
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Transition from triple helix to coil of Lentinan in solution measured by SEC, viscometry, and C-13 NMR
- 2002
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Ingår i: Polymer journal. - : Springer Science and Business Media LLC. - 0032-3896 .- 1349-0540. ; 34:6, s. 443-449
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Tidskriftsartikel (refereegranskat)abstract
- Lentinan, beta-(1 --> 3)-D-glucan with (1 --> 6) branching, was isolated from Lentinus edodes. Weight-average molecular weight M-w radius of gyration < s(2) > (1/2) and intrinsic viscosity [eta] of Lentinan in 0.2 M NaCl aqueous solution, dimethylsulfoxide (DMSO) and water/DMSO mixtures were measured by light scattering (LS), size exclusion chromatography (SEC) combined with LS, and viscometry. The results indicated that the glucan exists mainly as triple-helical chains in 0.2 M NaCl aqueous solution and water/DMSO mixtures with over 20 wt% water content, and as single-flexible chain in DMSO. The data from SEC-LS, viscosity and C-13 NMR measurements proved strongly that the helix-coil conformation transition occurred in a narrow range from 80 to 85 wt% DMSO aqueous solution, accompanying with obvious changes of M-w, < s(2) >(1/2)(z), [eta] as well as signals of C6 and C6(s). The transition of Lentinan in water/DMSO mixture was irreversible. The difference in C-13 NMR spectra for the triple-helical and coil conformations was the disappearance of the signals of C3 in beta-(1 --> 3)- linked backbone and the enhancement in relative intensities of glucose substituted C6s in the helix state, as well as the appearance of an asymmetric and broad peak of C6 in the intermediate of the conformation change. This suggests that the immobilization of the backbone by binding with intra and intermolecular hydrogen bonds resulted in the loss of the signals of its carbon atoms in the triple helix state. An overcoating cylinder model composed of the beta-(1 --> 3)- linked backbone as helix core and the side chains as rotatable overcoat was proposed to illustrate the triple-helical conformation and its transition in the solution.
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