2008
DOI: 10.1016/j.polymdegradstab.2007.11.011
|View full text |Cite
|
Sign up to set email alerts
|

Dependence of ultraviolet absorbers' performance on ultraviolet wavelength

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
24
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 27 publications
(24 citation statements)
references
References 22 publications
0
24
0
Order By: Relevance
“…Comparing the additives, HALS was the most efficient and the UV absorber not very different from the pure PP, especially after 15 weeks exposure. This may be caused by the consumption of the absorber by chemical reactions or by additive losses caused by diffusion and evaporation . The low efficient of the UV absorber is somewhat surprising as this is one of the types suggested to be used with PP and the concentration chosen is within the range that the manufacturer recommends.…”
Section: Resultsmentioning
confidence: 99%
“…Comparing the additives, HALS was the most efficient and the UV absorber not very different from the pure PP, especially after 15 weeks exposure. This may be caused by the consumption of the absorber by chemical reactions or by additive losses caused by diffusion and evaporation . The low efficient of the UV absorber is somewhat surprising as this is one of the types suggested to be used with PP and the concentration chosen is within the range that the manufacturer recommends.…”
Section: Resultsmentioning
confidence: 99%
“…But the catalyst loading is high (3.3%) and the coupling between acetyl chloride with boronic acid remains unsuccessful 6g,7a or only in moderate yields. Also the coupling between acetic anhydride with arylboronic acid has been reported by Gooben 5f by using Pd(OAc) 2 as catalyst, expensive P(p-MeOPh) 3 as ligand, and excess of arylboronic acid. Scheme 2.…”
Section: Studies On the Acylodeboronation Reaction Of Arylboronic Acimentioning
confidence: 93%
“…As shown in Table 4, the carbonylation yields were influenced by electron effect. Arylboronic acids with electron-rich groups such as CH 3 or CH 3 O, as well as 1-naphthyl motif could be coupled with acetic anhydride in moderate to good yields (Table 4, entries 1-5). When arylboronic acids bearing electron-deficient groups were applied, moderate yields were still obtained (Table 4, entries 6-8).…”
Section: Studies On the Acylodeboronation Reaction Of Arylboronic Acimentioning
confidence: 99%
See 1 more Smart Citation
“…These substances have a high steric hindrance in the molecule and must be highly stable in order not to be consumed so fast in secondary reactions other than stabilization [12,13].…”
Section: Introductionmentioning
confidence: 99%