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2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures

2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures

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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).

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