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Environmental

NewRxi™-1 ms Capillary GC Column

For Low Level GC/MS Analyses

By

Robert Freeman, Environmental Innovations Chemist

• Inert, low-bleed column for reliable result s.

Save time - analyze acidic and basic compounds under the same conditions.

Guaranteed reproducible performance, column to column.

The second column in our new

Rxi"

GC column

line - the Rxi™-lms column - will provide the

same outstanding performance as the Rxi™-Sms

column, with equally superior inertness, ultr a-low

bleed, and excellent batch to batch reproducibility.

Our first test for this 100% dimethylpolysiloxane

phase column was an analysis of a comple x mix­

ture of semivolatile organic compounds . The

extensive target list was comprised of many classes

of compounds including chloro acet ani lides,

chlorotriazines, tria zinon es, uracils, polcyclic aro­

matic hydrocarbons, and phthalates. Figure 1

shows peak shape and selectivity are equally good

for all of these diverse compounds, and all are elut­

ed in an acceptable analysis time .

Excellent Inertness

In addition to analyzing these compounds, we

analyzed an acidic compound (2,4-dinitrophenol)

and a basic compound (pyridine), each at O.5ng on

column, to assess column inertness. Column activ­

ity reveals itself through poor response and peak

tailing for such active compounds, and these two

compounds present both varying difficulties in a

GC/MS analysis and differing modes of degrad a­

tion . Figure 2 shows the excellent peak shapes and

respons es for these compounds on th e 30m x

0.25mm !D, 0.25flm film column.

Pheno ls are notorious for breakdown and peak

tailing, caused by interaction with the surface of an

active inlet liner or an active column. Nitrophenols

and pentachlorphenol, for exampl e, very often

exhibit poor peak shape and /or poor response.

Figure 3 shows the 30m x 0.2Smm !D, 0.2Sflm

Rxi™_lms column provi des very good peak

shapes for pheno ls. Peak responses are well above

method requirements.

Ultra-Low Bleed

In addition to excellent inertness, Rxi

H I

-l ms

columns exhibit very low bleed. Figure 4 is focused

on the end of the chromatogram for semivolatiles.

At 330°C, bleed is much lower than the signals for

O.5ngof target ana lytes. This exceptional signal-to­

no ise differential for late eluting compounds

assures better detection limits.

Figure 1

Excellent select ivity and peak shapes for common

drinking water semivolatiles at lOng, using an Rxi™-lms column.

1. 2-fluorophenol (surr.)

21. 2-naphthalenamine

42. metolachlor

2. bis(2-chloroethyl)ether

22. 5-nitro-o-toluidine

43.fluoranthene

3. phenol-d6(surr.)

23. diethylphthalate

44. pyrene

4. 1,4-dichlorobenzene-d4

24.fluorene

45. butachlor

(int. std.) •

25. propachlor

46. p-terphenyl-d14(surr.)

5. nitrobenzene-d5(surr.)

26. diphenylamine

47. p-dimethylaminoazobenzene

6. naphthalene-d8 (int. std.) •

27. 2,4,6-tribromophenol (surr.)

48. benzylbutyl phthalate

7. naphthalene

28.simazine

49. 2-acetylaminofluorene

8. l- rnethylnaphthalene

29.prometon

50. bis(2-ethylhexyl)adipate

9. 2-methylnaphthalene

30. atrazine

51. benzo(a)anthracene

10. hexachlorocyclopentadiene

31. hexachlorobenzene

52. chrysene-d12(int. std.) •

11. EPTC

32. 4-aminobiphenyl

53. chrysene

12. 2-fluorobiphenyl (surr.)

33. terbacil

54. bis(2-ethylhexyl)phthalate

13. 2,6-dinitrotoluene

34. phenanthrene-dl0 (int. std.) • 55. di-n-octylphthalate

14. dimethylphthalate

35. phenanthrene

56. benzo(b)fluoranthene

15. acenaphthylene

36. anthracene

57. benzo(k)fluoranthene

16. acenaphthene-dl fl (int. std.) • 37. metribuzin

58. benzo(a)pyrene

17. acenaphthene

38. acetochlor

59.perylene-d12(int. std.) •

18. 2,4-dinitrotoluene

39. alachlor

60. indeno(1,2,3-cd)pyrene

19. I-naphthalenamine

40. bromacil

61. dibenzo(a,h)anthracene

20. molinate

41. di-n-butylphthalate

62. benzo(ghi)perylene

2,3

13-36

6

4445

51,:%53

4

7 9 12

3~1

43

1/

46 50

8

381 42

4/ 8

54 55

57 59

1

10

37

56 58

40

6~rt

II

!

15.00

11,00

GC EV00833

Column:

Rx

i~-lms

,

30m, 0.25mm

10,

0.251lm

(cat.# 13323)

Sample:

US

EPA Method525.2 mix: custom525.2calibrationmix,

SVInternal Standard Mix (cat.# 31206),

BIN

Surrogate Mix

(4/89

SOW) (cat.# 31024),

Acid Surrogate Mix

(4/89

SOW) (cat.# 31025)

Inj.:

1.01lL,

lOllg/ mL

each analyte (internal standards

lOOllg/ mL),

split (10:1)

4mmDnlled Uniliner" inlet liner (holeat bottom) (cat.# 20756)

Instrument:

Agllent 6890

Inj. temp.:

250' C

Carrier gas:

helium, constant flow

Flow rate:

1.2mL/min.

Oven temp.:

50'C(hold 1 min.)to 265' C

@

20' C/ min., to 330'C

@

6'Cmin. (hold1 min.)

Del.:

Agilent 5973MSD

Transfer line

temp.:

280'C

Scanrange:

restek

innovation !

35-550 amu

Solventdelay: 3.20 min.

Tune:

DFTPP

DrilledUniliner"'- see page11.

Ionization:

EI

Website :

www.chromtech.net.au

E-mail :

info@chromatech.net.au

TelNo : 03 9762 2034 . . . in AUSTRALIA