“…In case of the iPP/C-PA, the t 1/2 are similar to those of neat iPP if the T c,iso is, again, below 130°C. In connection with previous study of the thermal stability of the esterified materials (Janicek et al 2013), one can presume, the material tends to degrade at the higher temperatures, which may influence the speed of crystallization. The vicinity of t 1/2 in case of neat iPP and iPP/C-PA at low temperatures could be explained after revealing the filler distribution and dispersion with the microscopy as described below.…”
Section: Resultsmentioning
confidence: 83%
“…On the other hand, the cellulose modified with OA showed similar water adsorption (hydrophility) as the PAmodified one (Janicek et al 2013). The slightly hydrophilic character of the C-OA may thus result in poor surface interaction with the matrix and inappropriate dispersion in comparison with the iPP/C-DA.…”
Section: Optical Microscopymentioning
confidence: 95%
“…The fibers were high-purity cellulose (99.8 %) with a relative density of 0.6, 50-350 lm in length; their diameter was in the range of 12-15 lm and the crystallinity of 65 % (data provided by the supplier). To increase the hydrophobicity of the cellulose, the material was surfaceesterified with oleic acid (OA), decanoic acid (DA) and propionic acid (PA) as described elsewhere (Uschanov et al 2010;Janicek et al 2013). The used method then gave cellulose with a degree of substitution (DS, calculated from XPS data) of about 1.49 and 1.25 in case of DA and OA, respectively (Uschanov et al 2010).…”
Section: Methodsmentioning
confidence: 99%
“…A previous article (Janicek et al 2013) showed that the modification reduces the hydrophility among the tested materials particularly in the decanoyl ester. On the other hand, the cellulose modified with OA showed similar water adsorption (hydrophility) as the PAmodified one (Janicek et al 2013).…”
Section: Optical Microscopymentioning
confidence: 98%
“…In some cases, the esterification may primarily influence the content of the b-phase polypropylene polymorph (Borysiak 2009); in others, the impact of surface modification is mainly negative, since the epitaxiality is usually disturbed, as shown, for example, by Borysiak (2012) with wood esterified with propionic or succinic anhydrides. The question then arises concerning whether the hydrophobization done with long carboxylic acids (Uschanov et al 2010;Janicek et al 2013) enables some nucleation activity or the epitaxial surface is modified to such an extent that no nucleation can occur. Uschanov et al (2010) also showed the different degrees of substitution achievable with various acids and noted the phenomenon connected with a lower degree of substitution when long or unsaturated acids are used.…”
Cellulose powders hydrophobized by surface esterification with carboxylic acids with different chain lengths (3, 10 and 18 carbons) were dispersed in a polypropylene matrix. Quality of the dispersion and nucleation activity of the filler were investigated by means of differential scanning calorimetry and optical microscopy. The results showed that the esterification decreases the crystallization rate in case of cellulose esterified with propionic or decanoic acid. On the other hand, the oleic acid ester demonstrated slightly higher crystallization rates than the unmodified cellulose, which was ascribed primarily to the newly arisen non-esterified surface after disintegration of the filler. Optical microscopy with hot stage showed the high nucleation ability of the natural cellulose fiber and its suppression in case of esterified surfaces. A complete inability to nucleate polypropylene crystallization was observed in case of decanoyl ester, while the other two retained some activity, but lower than that of the natural fiber. Finally, analysis of the filler dispersion and distribution revealed that the decanoyl and octadecanoyl esters disintegrate during melt mixing, while both dispersion and distribution of the fibers modified with propionic acid are poor.
“…In case of the iPP/C-PA, the t 1/2 are similar to those of neat iPP if the T c,iso is, again, below 130°C. In connection with previous study of the thermal stability of the esterified materials (Janicek et al 2013), one can presume, the material tends to degrade at the higher temperatures, which may influence the speed of crystallization. The vicinity of t 1/2 in case of neat iPP and iPP/C-PA at low temperatures could be explained after revealing the filler distribution and dispersion with the microscopy as described below.…”
Section: Resultsmentioning
confidence: 83%
“…On the other hand, the cellulose modified with OA showed similar water adsorption (hydrophility) as the PAmodified one (Janicek et al 2013). The slightly hydrophilic character of the C-OA may thus result in poor surface interaction with the matrix and inappropriate dispersion in comparison with the iPP/C-DA.…”
Section: Optical Microscopymentioning
confidence: 95%
“…The fibers were high-purity cellulose (99.8 %) with a relative density of 0.6, 50-350 lm in length; their diameter was in the range of 12-15 lm and the crystallinity of 65 % (data provided by the supplier). To increase the hydrophobicity of the cellulose, the material was surfaceesterified with oleic acid (OA), decanoic acid (DA) and propionic acid (PA) as described elsewhere (Uschanov et al 2010;Janicek et al 2013). The used method then gave cellulose with a degree of substitution (DS, calculated from XPS data) of about 1.49 and 1.25 in case of DA and OA, respectively (Uschanov et al 2010).…”
Section: Methodsmentioning
confidence: 99%
“…A previous article (Janicek et al 2013) showed that the modification reduces the hydrophility among the tested materials particularly in the decanoyl ester. On the other hand, the cellulose modified with OA showed similar water adsorption (hydrophility) as the PAmodified one (Janicek et al 2013).…”
Section: Optical Microscopymentioning
confidence: 98%
“…In some cases, the esterification may primarily influence the content of the b-phase polypropylene polymorph (Borysiak 2009); in others, the impact of surface modification is mainly negative, since the epitaxiality is usually disturbed, as shown, for example, by Borysiak (2012) with wood esterified with propionic or succinic anhydrides. The question then arises concerning whether the hydrophobization done with long carboxylic acids (Uschanov et al 2010;Janicek et al 2013) enables some nucleation activity or the epitaxial surface is modified to such an extent that no nucleation can occur. Uschanov et al (2010) also showed the different degrees of substitution achievable with various acids and noted the phenomenon connected with a lower degree of substitution when long or unsaturated acids are used.…”
Cellulose powders hydrophobized by surface esterification with carboxylic acids with different chain lengths (3, 10 and 18 carbons) were dispersed in a polypropylene matrix. Quality of the dispersion and nucleation activity of the filler were investigated by means of differential scanning calorimetry and optical microscopy. The results showed that the esterification decreases the crystallization rate in case of cellulose esterified with propionic or decanoic acid. On the other hand, the oleic acid ester demonstrated slightly higher crystallization rates than the unmodified cellulose, which was ascribed primarily to the newly arisen non-esterified surface after disintegration of the filler. Optical microscopy with hot stage showed the high nucleation ability of the natural cellulose fiber and its suppression in case of esterified surfaces. A complete inability to nucleate polypropylene crystallization was observed in case of decanoyl ester, while the other two retained some activity, but lower than that of the natural fiber. Finally, analysis of the filler dispersion and distribution revealed that the decanoyl and octadecanoyl esters disintegrate during melt mixing, while both dispersion and distribution of the fibers modified with propionic acid are poor.
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