2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Chem. Listy, 102, s265–s1311 (2008) Environmental Chemistry & Technology<br />
Fig. <strong>2.</strong> Volatile degradaction products of polyurethane foam<br />
sorbed on PDMS fibre<br />
1: 2-methyl-1,3-dioxane, 2: 2,4-diisocyanatotoluene, 3: 6,10dimethyl-5,9-undecadiene-2-one,<br />
4: 2,5-diterc-butyl-1,4-benzochinone,<br />
5: pentadecane, 6: hexadecane, 7: 2,6-bis(1,1-dimethyethyl)-4-(1-oxopropyl)phenol,<br />
8: 1-methylester dodecanoic<br />
acid, 9: 4-decyl-morphline, 10: heptadecane, 11: 2,6,10,14-tetramethylpentadecane,<br />
12: isopropylester tetradecanoic acid,<br />
13: 4-undecyl-morpholine, 14: N,N-dimethyl-1-hexadecanamine,<br />
15: 4-tetradecyl-morpholine, 16: squalene, 17: 4-hexadecyl-morpholine<br />
Also nitrogen derivates were detected, namely line of<br />
alkyl-substitued morpholines and n,n-dimethyl-1-hexadecanamine.<br />
By the photolysis of hard segment of polyurethane foam<br />
2,5-diterc-butyl-1,4-benzochinone, 2,6-bis(1,1-dimethyethyl)-4-(1-oxopropyl)phenol<br />
and 2,4-diisocyanatotoluene<br />
(2,4-TDI) were formed.<br />
2,4-TDI is very volatile and toxic. The compound is<br />
used as main reagent at synthesis of polyurethane. 2,4-TDI<br />
was detected in case of all polymers modified by celulose<br />
derivate fillers. It is difficult to say whether that compound is<br />
photodegradation product of polyurethane foam or unreacted<br />
raw material residue. It will be studied in the next research.<br />
All the compounds were detected in most polyurethane<br />
samples. There was observed qualitative change only.<br />
Quantitative differences were found in the case of minority<br />
distribution compounds. Their identification using library<br />
search in nIST 05 was unsuccessful in most cases. Probably<br />
small concentrations of analyte and resulting low-intensity<br />
mass spectra could be the reason, or – due to specific character<br />
of volatile compound made by irradiation of polyurethane<br />
foam – their mass spectra are not included in this library.<br />
PA fibre shows higher selectivity in comparison with<br />
PDMS fibre which in opposite gives more complex information<br />
about volatile compounds formed during photodegradation<br />
of polyurethane.<br />
s352<br />
Fig. 3. Volatile degradaction products of polyurethane foam<br />
sorbed on PA fibre<br />
1: 2-(2-ethoxyethoxy)-ethanol, 2: 2-ethyl-hexanoic acid, 3: 1,3dioxane,<br />
4: 2-methyl-1,3-dioxolane, 5: 2-methyl-1,3-diisocyanatobenzene,<br />
6: 2,6-bis(1,1-dimethyethyl)-4-(1-oxopropyl)phenol,<br />
7: 4-decyl-morpholine, 8:4-undecyl-morpholine, 9: N,N-dimethyl-1-hexadecanamine,<br />
10: 4-tetradecyl-morpholine, 11: 4-hexadecyl-morpholine<br />
Conclusions<br />
In this study the SPME method was applied for the<br />
identification of volatile compounds formed by irradiation<br />
of polyurethane foams modified by biodegradable fillers. A<br />
wide range of compounds was detected and most of them<br />
were succesfully identified by library search. The identification<br />
of the remaining compounds will be a subject of the next<br />
research.<br />
The finantial support from the project no.MSM<br />
0021630501 from Ministry of Education, Youth and Sport of<br />
the CR is greatly acknowledged.<br />
REFEREnCES<br />
1. Philippart J. L., Posada F., Gardette J. L.: Polym. Degr.<br />
Stab. 285, 49 (1995).<br />
<strong>2.</strong> Albertsson A. Ch., Karlsson S.: Polym. Degr. Stab. 245,<br />
41 (1993).<br />
3. Khabbaz F., Albertsson A. Ch., Karlsson S.: Polym.<br />
Degr. Stab. 329, 61 (1998).<br />
4. Carlsson D. J., Krzymien M., Worsfold D. J., Day M.: J.<br />
Vinyl. Add. Techn. 3, 2 (1997).<br />
5. Hakkarainen M., Albertsson A. Ch., Karlsson S.: J. chromatogr.<br />
A. 741, 251 (1996).<br />
6. Dannoux A., Esnouf S., Begue J., Amekraz A., Moulin<br />
C.: nucl. Instr. Meth. Phys. Res. B. 236, 488 (2005).<br />
7. Irusta L., Fernandez-Berridi M.J.: Polymer 40, 4821<br />
(1999).