The paper presents our results concerning the ultrasonically assisted extraction of bioactive principles from plant material. A comparison with classical methodologies is presented and technological aspects of ultrasonically assisted extraction are discussed.

No abstract

Glycolysis of PET waste with isosorbide, a biomass derived diol, was catalyzed by commercially available 1,5,7-triazabicyclo [4.4.0] dec-5-ene (TBD) at temperature up to 190�C when low molecular weight oligomer containing at least one equivalent of isosorbide was obtained. The structural assignment of the oligomer product was established by NMR spectroscopy showing predominantly end-chain bonded isosorbide with exo/endo ratio of 55/45. Mechanistic considerations of the transesterification reaction of isosorbide with dimethylterephthalate (DMT) as model reaction revealed that the hydrogen bonding interaction of TBD with this diol is the favored mechanism pathway. This was established by corroborating solution NMR spectroscopy studies with DFT calculations at B3LYP level where it was observed that isosorbide is hydrogen bonded to TBD through both endo and exo hydroxyl groups. On the other hand, the TBD catalyst reacts with dimethylterephthalate at low temperature forming a stable, easy to handle covalently bonded adduct.

Die aus den Phenacylbromiden (II) mit Chinazolin (I) zugänglichen Phenacylchinazoliniumbromide (III) liefern mit Propylenoxid (IV) über die nicht isolierten Ylide (V) neben (I) die Pyrrolochinazoline (VI).

Following the green chemistry principles, three series of polyols with tailored chemical structures were obtained from PET wastes degradation via glycolysis and/or aminolysis and subsequent esterification-transesterification and/or amidation reactions, using an organic catalyst. As cleaving agents there were used various mixtures of renewable or potentially renewable reagents, selected from those that can be obtained from biomass by already applied or investigated and eventually patented biochemical and/or chemical processes. The polyols were characterized by physical-chemical methods, 1H-NMR, 13C-NMR and FT-IR Spectroscopy, and tested in the synthesis of rigid polyurethane foams, showing appropriate properties for spray foams formation and leading to materials with properties similar to conventional spray foams.