Composition and Structure of Ethanol-Lignins of Coniferous and Deciduous Wood and Products of their Catalytic Telomerization with 1,3-Butadiene

The composition and structure of ethanol-lignins of coniferous (abies, pine) and deciduous (aspen, birch) wood and products of their catalytic telomerization with 1,3-butadiene has been studied with use of the methods 31P-NMR, gel-permeation chromatography, scanning electron microscopy and elemental analysis. Data on the nature and content of hydroxyl groups in ethanol-lignins were obtained using phosphorylation of lignins with 2-chloro‑4,4,5,5,-tetramethyl‑1,3,2-dioxaphospholane.The studied lignins differ from each other in the content of aliphatic, phenolic and carboxyl groups. The total content of hydroxyl groups increases in the series of ethanol-lignins: birch < aspen < pine < abies. For the modification of ethanol-lignins, the reaction of catalytic telomerization with 1,3-butadiene was used at 70 °C and 90 °C in the presence of a complex of palladium (II) diacetate with the sodium salt of triphenylphosphine trisulfate. By comparing the number of aliphatic, phenolic and carboxyl OH- groups in the initial and telomerized ethanol-lignins, it was found that only aliphatic and phenolic hydroxyl groups participate in the telomerization reaction. Telomerization of ethanol-lignins with 1,3-butadiene increases their average molecular weight and reduces polydispersity. The morphology of telomerized and initial samples of ethanol-lignins varies significantly

Synthesis of pH-Responsive Copolymer PVA/PDEAEMA by ATRP

In this paper, the macroinitiator (PVAc-Cl) was prepared from vinyl acetate telomerization reaction by using BPO as initiator and CCl4 or CHCl3 as chain transfer agent. Then the pH-responsive PVAc /poly (2-(dimethylamino) ethyl methacrylate) (PVAc/PDEAEMA) were synthesized via atom transfer radical polymerization (ATRP) and evidenced by FTIR spectroscopy. PVA/PDEAEMA were synthesized by alcoholysis PVAc/PDEAEMA and evidenced by FTIR spectroscopy.