1997
DOI: 10.1002/(sici)1099-0488(199703)35:4<595::aid-polb7>3.3.co;2-o
|Get access via publisher |Summarize |Cite
|
Sign up to set email alerts

Temperature‐induced phase transition of poly(N,N‐dimethylaminoethyl methacrylate‐co‐acrylamide)

Search citation statements

Order By: Relevance

Paper Sections

Select...
27
14
12
2

Citation Types

4
63
1
0

Year Published

1997
1997
2021
2021

Publication Types

Select...
47
2
1

Relationship

2
48

Authors

Journals

citations

Cited by 50 publications

(68 citation statements)
references

References 0 publications

4
63
1
0
Order By: Relevance
How this paper cites the one you are viewing
“…In apparent contradiction to previous work, 16,17 our copolymer gels show that the heat associated with the volume transition decreases with an increase in the hydrophobic alkyl chain length. Our theoretical predictions of the heat of demixing are also in qualitative agreement with experimental observations.…”
Section: Discussion
contrasting
confidence: 99%
How this paper cites the one you are viewing
“…In apparent contradiction to previous work, 16,17 our copolymer gels show that the heat associated with the volume transition decreases with an increase in the hydrophobic alkyl chain length. Our theoretical predictions of the heat of demixing are also in qualitative agreement with experimental observations.…”
Section: Discussion
contrasting
confidence: 99%
How this paper cites the one you are viewing
“…The LCST of the HPC- g -PDMAEMA shifts to lower temperature than that of HPC is probably due to the formation of hydrogen bonds between the hydroxyl groups on HPC backbone (as a hydrogen bond donor) and the dimethylamino groups or the ester groups in PDMAEMA (as a hydrogen bond acceptor), which screens the hydrophilic groups in HPC from exposing to water and results in a hydrophobic contribution to the LCST of HPC. Similar results have been reported by Cho and Yuk . The above results demonstrate that the phase transition mechanism of the HPC 0.1 - g -PDMAEMA 20 aqueous solution differs from that of HPC.…”
Section: Results
supporting
confidence: 91%
How this paper cites the one you are viewing
“…As shown in Figure 8, the cloud points for the copolymers of these two monomers are lower than those of the homopolymers for almost all compositions, because of the hydrogen bonding between acid and ether units. Similar effects have been observed in graft copolymers composed of NIPAM and acrylic acid,6 and copolymers of 2‐(dimethylamino)ethyl methacrylate with either acrylamide30 or N ‐ethylacrylamide 31…”
Section: Results
supporting
confidence: 70%