In Situ Formation of Protein–Polymer Conjugates through Reversible Addition Fragmentation Chain Transfer Polymerization

2007 ◽  
Vol 119 (17) ◽  
pp. 3159-3163 ◽  
Author(s):  
Jingquan Liu ◽  
Volga Bulmus ◽  
David L. Herlambang ◽  
Christopher Barner-Kowollik ◽  
Martina H. Stenzel ◽  
...  
2007 ◽  
Vol 46 (17) ◽  
pp. 3099-3103 ◽  
Author(s):  
Jingquan Liu ◽  
Volga Bulmus ◽  
David L. Herlambang ◽  
Christopher Barner-Kowollik ◽  
Martina H. Stenzel ◽  
...  

2021 ◽  
Author(s):  
Eun Ho Lee ◽  
Kyungho Kim ◽  
Gyeongdong Yeom ◽  
Bongkuk Seo ◽  
Wonjoo Lee ◽  
...  

We report for the first time in situ reversible addition–fragmentation chain transfer (RAFT) dispersion polymerization in an epoxy resin mixture for toughening of epoxy. Good dispersion of latex particles in...


2017 ◽  
Vol 58 (2) ◽  
Author(s):  
Francisco Javier Enríquez-Medrano ◽  
Florentino Soriano-Corral ◽  
Pablo Acuña-Vázquez ◽  
Edgar N. Cabrera-Álvarez ◽  
Hened Saade-Caballero ◽  
...  

<p>Different rubbers based on polybutadiene were synthesized in solution by the reversible addition-fragmentation chain-transfer polymerization (RAFT) technique using 4-cyano-4-[(dodecylsulfanylthiocarbonyl)sulfanyl] entanoic acid as RAFT agent and 1,1’-azobiscyclohexanecarbonitrile (Vazo-88) as initiator. The results obtained in the polymerization of polybutadiene and poly(butadiene-<em>co</em>-acrylonitrile) (NBR) are discussed in terms of molecular weight distribution, composition and microstructure. Composition of polybutadiene in NBR´s was kept constant along the copolymerization, and the vinyl, <em>cis</em> and <em>trans</em> isomers are shown in values of around 12, 26 and 62% in all cases. Resulting rubbers were used to synthesize acrylonitrilebutadiene-styrene (ABS) type resins through an <em>in situ</em> bulk polymerization. Dynamic-mechanical properties and the morphology were analyzed in all the different ABS resins. In DMA analyses, the rubber component presented two transitions as well as an increase in the magnitude of the transition located around -75 °C, which is explained by the significant amount of SAN occlusions in the morphology, analyzed by TEM.</p>


2013 ◽  
Vol 66 (2) ◽  
pp. 337-344 ◽  
Author(s):  
Masoud Sobani ◽  
Vahid Haddadi-Asl ◽  
Mehdi Salami-Kalajahi ◽  
Hossein Roghani-Mamaqani ◽  
Seyed-Ataollah Mirshafiei-Langari ◽  
...  

e-Polymers ◽  
2020 ◽  
Vol 20 (1) ◽  
pp. 317-327
Author(s):  
Chenliang Shi ◽  
Ling Lin ◽  
Yukun Yang ◽  
Wenjia Luo ◽  
Maoqing Deng ◽  
...  

AbstractThe influence of density of amino groups, nanoparticles dimension and pH on the interaction between end-functionalized polymers and nanoparticles was extensively investigated in this study. PS–NH2 and H2N–PS–NH2 were prepared using reversible addition–fragmentation chain transfer polymerization and atom transfer radical polymerization. Zero-dimensional carbon dots with sulfonate groups, one-dimensional cellulose nanocrystals with sulfate groups and two-dimensional graphene with sulfonate groups in the aqueous phase were added into the toluene phase containing the aminated PS. The results indicate that aminated PS exhibited the strongest interfacial activity after compounding with sulfonated nanoparticles at a pH of 3. PS ended with two amino groups performed better in reducing the water/toluene interfacial tension than PS ended with only one amino group. The dimension of sulfonated nanoparticles also contributed significantly to the reduction in the water/toluene interfacial tension. The minimal interfacial tension was 4.49 mN/m after compounding PS–NH2 with sulfonated zero-dimensional carbon dots.


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