Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Casey D. Stokes"'
Autor:
Ajay Singh Negi, Fatemeh Khalkhal, Casey D. Stokes, James J. Harrison, David L. Morgan, Chinedum O. Osuji
Publikováno v:
Langmuir : the ACS journal of surfaces and colloids. 34(3)
Maintaining suspension stability by effective particle dispersion in systems with attractive interactions can be accomplished by the addition of dispersants that modify the interparticle potential to provide steric or electrostatic barriers against a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::423ea2d377210747af022505ba3e70e4
https://pubmed.ncbi.nlm.nih.gov/29095629
https://pubmed.ncbi.nlm.nih.gov/29095629
Autor:
Robson F. Storey, Subramanyam Ummadisetty, Casey D. Stokes, Christopher G. Campbell, James J. Harrison, David L. Morgan
Publikováno v:
Macromolecular Symposia. 323:6-17
exo-Olefin-terminated polyisobutylene was obtained directly from living isobutylene polymerizations by addition of a quenching compound to the living chain ends. Three broad classes of compounds were evaluated including hindered bases such as hindere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb5aea05448a3099b5844eab3823cc0e
https://doi.org/10.1002/masy.201200017
https://doi.org/10.1002/masy.201200017
Autor:
Wim van Dam, Keith Narasaki, Casey D. Stokes, Ken Nelson, Kevin D. Carabell, James A. Mcgeehan, James A. Rutherford, Sheila W. Yeh, Alexander B. Boffa
Publikováno v:
SAE International Journal of Fuels and Lubricants. 5:1240-1263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8654e17232539bfe07f2ea040335df2
https://doi.org/10.4271/2012-01-1709
https://doi.org/10.4271/2012-01-1709
Publikováno v:
Macromolecules. 44:7901-7910
exo-Olefin (methyl vinylidene)-terminated polyisobutylene (PIB) was synthesized in one pot by quenching TiCl4-catalyzed living PIB with a dialkyl (or) diaryl sulfide at −60 to −40 °C, followed by a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cdc88b6d9e56a45bf048a50177ec194
https://doi.org/10.1021/ma201728a
https://doi.org/10.1021/ma201728a
Publikováno v:
Macromolecules. 44:2438-2443
Kinetic investigation of end-quenching (β-proton abstraction to form exo-olefin) of quasiliving polyisobutylene (TiCl4, −60 °C, 60/40 hexane/methyl chloride) with sterically hindered amines, 2-tert-butylpyridine (2TBP), 1,2,2,6,6-pentamethylpiper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb3024764bacb5bb7566b2b65e0aa1b7
https://doi.org/10.1021/ma200200v
https://doi.org/10.1021/ma200200v
Publikováno v:
Macromolecules. 42:2344-2352
Low-temperature-stable sulfonium ion adducts were generated by addition of mono- and disulfides to TiCl4-catalyzed quasiliving polyisobutylene (PIB). The adducts were studied in situ via low temperature NMR in 50/50 (v/v) CS2/CD2Cl2 using the initiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec1ed8c62f44689a3154afd7b0355e4d
https://doi.org/10.1021/ma802812m
https://doi.org/10.1021/ma802812m
Publikováno v:
Macromolecules. 38:4618-4624
Quasiliving isobutylene polymerization initiated by 2-chloro-2,4,4-trimethylpentane/TiCl4/2,6-dimethylpyridine in 60/40 n-hexane/methyl chloride at −70 °C was allowed to reach 98+% monomer conversion and then reacted with N-methylpyrrole. All poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cbddaa6ad8d5501c2c293d39941a5ea
https://doi.org/10.1021/ma0474628
https://doi.org/10.1021/ma0474628
Autor:
Casey D. Stokes, Robson F. Storey
Publikováno v:
In Situ Spectroscopy of Monomer and Polymer Synthesis ISBN: 9781461349358
We have conducted a series of kinetic investigations on controlled cationic isobutylene (IB) polymerizations at high temperature, i.e., -10°C, monitored using in situ ATR-FTIR spectroscopy (ReactIR 1000, ASI Applied Systems,Inc.). The polymerization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d22dd5475042664b6093e118eae443b
https://doi.org/10.1007/978-1-4615-0125-1_4
https://doi.org/10.1007/978-1-4615-0125-1_4
Publikováno v:
Macromolecules; Oct2011, Vol. 44 Issue 20, p7901-7910, 10p
Publikováno v:
Macromolecules; Apr2011, Vol. 44 Issue 8, p2438-2443, 6p