1996
DOI: 10.1002/(sici)1099-0518(19960730)34:10<1907::aid-pola8>3.3.co;2-d
|Get access via publisher |Summarize |Cite
|
Sign up to set email alerts

Synthesis and impact properties of siloxane–DGEBA epoxy copolymers

Search citation statements

Order By: Relevance

Paper Sections

Select...
5
3
2
0

Citation Types

1
10
0
0

Year Published

2000
2000
2022
2022

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations

Cited by 10 publications

(11 citation statements)
references

References 0 publications

1
10
0
0
Order By: Relevance
How this paper cites the one you are viewing
“…The 1 H‐NMR spectrum of E‐S10 copolymer is displayed in Figure . 1 H‐NMR spectrum shows the chemical shifts (δ, in ppm from TMS = 0) at 7.25–6.81 (protons‐phenyl‐), 4.17 (HCOSi), 3.34 (HCoxirane), 2.89, 2.74 (H 2 Coxirane), 1.63 [(CH 3 ) 2 C], and 0.07 (H 3 CSi) . The experimental data of chemical shifts are in accordance with that of the structure of the theoretical assumption.…”
Section: Results
supporting
confidence: 80%
“…And the appearance of characteristic peaks of SiOSi (1030 cm −1 ) and SiOC (1130 cm −1 ) significantly indicates that the PMPS is successfully grafted onto the E51 with retention of the oxirane group in the epoxy structure. Besides, the characteristic absorption peaks at 3500, 2840, 1590, and 1430 cm −1 , 2960 and 1250 cm −1 are attributed to the hydroxyl, SiOCH 3 , Si‐C 6 H 5 , and SiCH 3 groups …”
Section: Results
mentioning
confidence: 99%
See 1 more Smart Citation