Plastics Testing and Characterization 2008
DOI: 10.3139/9783446418530.fm
|View full text |Cite
|
Sign up to set email alerts
|

Plastics Testing and Characterization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
10
0

Year Published

2012
2012
2022
2022

Publication Types

Select...
4
1

Relationship

1
4

Authors

Journals

citations
Cited by 7 publications
(13 citation statements)
references
References 0 publications
0
10
0
Order By: Relevance
“…The second is due to the lower viscosity of PEG compared to UHMWPE and PP that easily migrate to the skin layer of the melt where the shear rate is maximum. According to Naranjo et al [ 22 ], surface tension between two materials appears as a result of different intermolecular interactions and was found to play a significant role in the deformation of polymers during flow, especially in dispersive mixing of polymer blends. Based on this paper, a similar factor is expected to contribute in the melt viscosity reductions of UHMWPE/HDPE/PEG blends.…”
Section: Resultsmentioning
confidence: 99%
“…The second is due to the lower viscosity of PEG compared to UHMWPE and PP that easily migrate to the skin layer of the melt where the shear rate is maximum. According to Naranjo et al [ 22 ], surface tension between two materials appears as a result of different intermolecular interactions and was found to play a significant role in the deformation of polymers during flow, especially in dispersive mixing of polymer blends. Based on this paper, a similar factor is expected to contribute in the melt viscosity reductions of UHMWPE/HDPE/PEG blends.…”
Section: Resultsmentioning
confidence: 99%
“…Figure 3 shows the infrared spectra of the greenhouse plastics, obtained by the ATR technique, (initial and after 18 months of exposure samples). The bands with the highest intensity at 2920, 2850, 1473, 1463, 730, and 720 cm −1 correspond to the characteristic signals of PE, 25,44 while the band at 875 cm −1 corresponds to the charge of the sample identified as calcium carbonate. The structural changes on the surface are evidenced in the bands of lower intensity, around 1720 cm −1 .…”
Section: Resultsmentioning
confidence: 97%
“…Infrared spectra of the surface of the samples were obtained by FTIR spectroscopy with a diamond crystal Attenuated Total Reflectance accessory. 25 The strongest bands were analyzed and compared with signals previously identified by transmittance FTIR. Finally, the structural changes of the surface of the samples were established.…”
Section: Methodsmentioning
confidence: 99%
“…Finally, in order to examine the curing mechanism, FTIR spectroscopy data are collected for the oligomer and the resin cured at 200°C for times up to 30 h. The representative absorption curves are shown in Figure . The peak at 2950 cm −1 represents the C–H stretching absorption; the peak at 2510 cm −1 is for the S–H thiol bond, and the peak at 1720 cm −1 is associated with the C=O in the carboxyl group . During the cure, the intensity of the S–H peak decreases with the time of curing whereas the intensity of the C–H and C=O remains relatively constant.…”
Section: Resultsmentioning
confidence: 99%
“…The peak at 2950 cm 21 represents the C-H stretching absorption; the peak at 2510 cm 21 is for the S-H thiol bond, and the peak at 1720 cm 21 is associated with the C5O in the carboxyl group. 50 During the cure, the intensity of the S-H peak decreases with the time of curing whereas the intensity of the C-H and C5O remains relatively constant. Note that, although the height of the C5O absorption peak decreases upon curing, the area under the peak is only about 3% lower.…”
Section: Articlementioning
confidence: 92%