Applications of Fourier Transform IR Spectroscopy in Fuel Science

Nov 12, 1982 - Petroleum reserves are limited and supplies are becoming expensive and unstable. Extensive efforts are underway in the United States an...
0 downloads 8 Views 3MB Size
4

A p p l i c a t i o n s of F o u r i e r T r a n s f o r m I R S p e c t r o s c o p y in F u e l Science

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

P. R. SOLOMON, D. G. HAMBLEN, and R. M. CARANGELO Advanced Fuel Research, Inc., East Hartford, CT 06108

Petroleum reserves are limited and supplies are becoming expensive and unstable. Extensive efforts are underway in the United States and abroad to find alternative sources for fuel and chemicals by employing coal, oil shale, tar sands, and biomass. But complicated processing of these raw materials is required to deliver environmentally acceptable products at a competitive price. It is, therefore, increasingly important to obtain better characterization of these raw materials and better understanding of their transformation in a process. Fourier Transform Infrared (FT-IR) Spectroscopy is one of the most versatile techniques available for providing analytical data on the raw materials, the process chemistry and the products. Dispersive infrared spectroscopy has traditionally been an important tool in fuel characterization since most organic and mineral components absorb in the IR. Discussions of applications to coal may be found in Lowry (1), van Krevlen (2), Friedel (3), Brown (4), Brooks, Durie and Sternhell C5) Friedel and Retcofsky (6) and references cited therein. But FT-IR with i t s advantages in speed, sensitivity and data processing has added new dimensions. The FT-IR permits rapid routine quantitative characterizations of solids, liquids and gases. The FT-IR's speed (a complete spectrum can be obtained in 80 msec) provides the possibility of following chemical transformations (such as coal

0097-6156/82/0205-0077$07.25/0 © 1982 American Chemical Society

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

78

COAL AND

COAL PRODUCTS

p y r o l y e i s ) as i t occurs or permits o n - l i n e a n a l y s i s of products subject to s e p a r a t i o n techniques such as LC, GC or solvent separation. The FT-IR provides h i g h s e n s i t i v i t y because of i t s high s i g n a l throughput and by co-adding s p e c t r a to produce good s i g n a l to n o i s e . This f e a t u r e permits measurement of h i g h l y absorbing m a t e r i a l s such as c o a l or the use of difficult techniques such as photoacoustic or diffuse reflectance spectroscopy. The l a t t e r techniques a l l o w measurement of s o l i d s w i t h minimal sample p r e p a r a t i o n . Other advantages of the FT-IR are d i g i t a l storage of s p e c t r a and the a v a i l a b i l i t y of many data a n a l y s i s r o u t i n e s which were developed to take advantage of the computer which an FT-IR r e q u i r e s . These r o u t i n e s permit such operations as base l i n e c o r r e c t i o n s , smoothing, s p e c t r a l comparisons, s p e c t r a l s y n t h e s i s , f a c t o r a n a l y s i s , c o r r e l a t i o n techniques, s o l v e n t subtraction, mineral subtraction, display and plotting flexibility and programmed c o n t r o l of experiments. These techniques have proved so u s e f u l that d i s p e r s i v e instruments are now being o f f e r e d w i t h add-on computers. As a r e s u l t of the above advantages of FT-IR, i n v e s t i g a t o r s have βtarted to reexamine a p p l i c a t i o n s i n f u e l science and technology. P a i n t e r et a l . (_7, 8) have proposed techniques f o r q u a n t i t a t i v e l y analyzing mineral components i n c o a l s and low temperature ash by using s u b t r a c t i o n r o u t i n e s and a quantitative mineral l i b r a r y . P a i n t e r a l s o has used FT-IR f o r studying c o a l o x i d a t i o n (9) and l i q u e f a c t i o n products (10, 11). Solomon has considered the a n a l y s i s of organic constituents. Calibration factorβ were determined f o r computing the a l i p h a t i c and aromatic hydrogen concentrations from the i n t e g r a t e d areas under the peaks near 2900 cm and 800 cm r e s p e c t i v e l y (12) and f o r determining the hydroxyl concentrations from the abeorbance at 3200 cm (13). From the aliphatic hydrogen concentration, a reasonable determination can a l s o be made of the a l i p h a t i c and aromatic carbon c o n c e n t r a t i o n using the Brown-Ladner r e l a t i o n (14) and an assumed a l i p h a t i c s t o i c h i o m e t r y . A p p l i c a t i o n s of q u a n t i t a t i v e a n a l y s i s of organic components have been a p p l i e d to c o a l proximate a n a l y s i s (15), o i l shale y i e l d s (16), p y r o l y e i s y i e l d s (17) and c o a l s t r u c t u r e (18). A p p l i c a t i o n s of FT-IR f o r a n a l y s i s of p y r o l y e i s gases has been discussed by E r i c k s o n et a l (19) and by Solomon and co-workers (20-23). The FT-IR*s rapid data a c q u i s i t i o n s (80 m sec/scan) a l s o allows p y r o l y e i s k i n e t i c s to be followed ( 2 0 - 2 3 ) . F i n a l l y , the FT-IR system operates by coding the i n f r a r e d source w i t h an amplitude modulation which i s unique to each i n f r a r e d frequency. The d e t e c t o r i s s e n s i t i v e to the modulated r a d i a t i o n so that unmodulated s t r a y r a d i a t i o n i s e l i m i n a t e d from the experiment, p e r m i t t i n g the use of the FT-IR as an in-situ detector i n many experiments. For example, an FT-IR has been used to monitor the e v o l u t i o n of c o a l p y r o l y e i s products w i t h i n a drop tube furnace (24) and w i t h i n an e n t r a i n e d flow r e a c t o r (25). The l a t t e r has been operated up to 1200°C.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

4.

SOLOMON ET AL.

Applications of FTIR

in Fuel Science

79

These a p p l i c a t i o n s o f FT-IR i n f u e l science are reviewed i n the f o l l o w i n g pages. The paper d e s c r i b e s techniques o f sample preparation, q u a n t i t a t i v e analysis of spectra for s o l i d s , l i q u i d s and gases and a p p l i c a t i o n s to hydrocarbon a n a l y s i s and conversion.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

Apparatus Most o f the measurementβ described i n t h i s paper were made w i t h a N i c o l e t model 7199 F o u r i e r Transform I n f r a r e d Spectrometer using a Globar source and a l i q u i d n i t r o g e n cooled mercury-cadmium t e l l u r i d e d e t e c t o r . For s o l i d s and l i q u i d s , good q u a l i t y s p e c t r a were obtained a t 4 wavenumber r e s o l u t i o n by co-adding 32 scans w i t h the IR beam t r a n s m i t t e d through the sample r a t i o e d t o a background o f 32 scans co-added i n the absence of the sample. Spectra are converted to absorbance s i n c e under the c o n d i t i o n s o f the measurement, Beer's Law i s expected to h o l d and the absorbance i s p r o p o r t i o n a l t o sample q u a n t i t y . For gases, h i g h r e s o l u t i o n spectra were obtained a t 0.5 wavenumberβ and r a p i d scan data were obtained at 8 wavenumbers. A n a l y s i s o f S o l i d Samples P r e p a r a t i o n o f KBr P e l l e t s Q u a n t i t a t i v e FT-IR t r a n s m i s s i o n s p e c t r a o f s o l i d s were obtained u s i n g f i n e l y ground samples pressed i n KBr p e l l e t s . Ten t o f i f t y mg o f sample taken from a ground (100 mesh o r f i n e r ) , w e l l mixed, r e p r e s e n t a t i v e sample were placed i n a s t a i n l e s s s t e e l g r i n d i n g capsule, d r i e d i n vacuum f o r s e v e r a l hours, b a c k f i l l e d w i t h dry n i t r o g e n , sealed i n the capsule and ground. The length o f g r i n d i n g time necessary to o b t a i n p a r t i c l e s which are s u f f i c i e n t l y f i n e ( f o r the IR r a d i a t i o n t o penetrate) depends on the shaker, amount and c h a r a c t e r i s t i c s of the sample and the g r i n d i n g capsule. A good r u l e t o f o l l o w i s t o g r i n d so that f u r t h e r g r i n d i n g does not change the i n t e n s i t y of the a b s o r p t i o n . For most samples, 20 minutes u s i n g a "Wig -L-Bug" shaker i s s u f f i c i e n t . M a t e r i a l s l i k e t a r sands which have l a r g e m i n e r a l g r a i n s and s o f t organic matter a r e among the most d i f f i c u l t to handle and must be ground c o l d ( t o freeze the organic matter)· A small sample ( t y p i c a l l y 1.0 mg but as low as 0.25 mg f o r h i g h carbon content c o a l s o r chars) o f t h i s f i n e l y ground dry sample i s weighed (to _+·01 mg) i n a dry box and added to a weighed amount (about 300 mg determined to +_ 0.1 mg) of KBr. The KBr and c o a l are then mixed by g r i n d i n g f o r 30 seconds and pressed i n t o a p e l l e t i n an evacuated d i e under 20,000 l b s pressure. The p e l l e t i s then weighed and the sample weight per cm o f p e l l e t area i s determined. The s p e c t r a f o r a c o a l (approximately 1 mg sample i n 300 mg KBr) prepared i n t h i s manner are shown i n F i g 1. The s p e c t r a f o r undried p e l l e t s show the presence o f absorbed water (peaks a t 3400cm , 1640cm and 600cm" ). The more KBr used and the longer the mixing d u r a t i o n , the l a r g e r the water peaks. -1

1

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

COAL AND COAL PRODUCTS

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

80

Figure 1.

FTIR spectra of a North Dakota lignite showing the effects of drying a KBr pellet sample up to 48 hours.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

4.

SOLOMON ET AL.

Applications of FTIR

in Fuel Science

81

Drying P e l l e t s to Remove Water The problem o f the KBr-H 0 bands i s discussed i n Refs. Q , 3^ 1_3 and 26). They appear only a f t e r g r i n d i n g the KBr. To remove them, i n v e s t i g a t o r s have t r i e d h e a t i n g the p e l l e t s w i t h v a r i a b l e success. F r i e d e l reported work of Tschamler which suggested that the complete removal o f the KBr-H^O bands occurred only when the p e l l e t s were measured a t 175°C ( 3 ) . Upon c o o l i n g , the bands reappeared, although at reduced i n t e n s i t y . Osawa and Shih d r i e d p e l l e t s f o r 2 days a t 60°C and found r e s i d u a l a b s o r p t i o n a t t r i b u t a b l e t o water (27). Roberts reported that d r y i n g a t 100 t o 110°C diminished o r e l i m i n a t e d the KBr-H^O bands (28). Solomon and Carangelo achieved good r e s u l t s by d r y i n g a t 110°C f o r 48 hours (13). For a pure KBr p e l l e t , t h i s procedure reduced the i n t e n s i t y o f the 3400 cm" band from .06 absorbance u n i t s i n the undried p e l l e t t o .01 absorbance u n i t s . For c o a l , these c o n d i t i o n s are a good choice s i n c e 104° t o 110°C i s the s p e c i f i e d d r y i n g temperature f o r determining c o a l moisture. The e f f e c t i v e n e s s o f h e a t i n g the p e l l e t s depends on the p e l l e t p r e p a r a t i o n procedure which i n c o r p o r a t e s the water and on the d r y i n g c o n d i t i o n s which removes i t . I n c o n s i d e r i n g the r e s u l t s o f Ref. (13) i t must be coneidered that the c o a l s were f i r e t d r i e d and ground and then mixed w i t h the KBr using a 30 eecond g r i n d so that a v a i l a b l e moisture from the c o a l i s minimized and long g r i n d i n g o f the KBr does not occur. The r e e u l t e o f d r y i n g a c o a l p e l l e t are i l l u e t r a t e d i n F i g . 1. The p e l l e t wae d r i e d i n vacuum at 105°C f o r 6, 12, 24, and 48 hours. The f i g u r e shows the s p e c t r a o f the undried pelleté, the apectra o f the pelleté d r i e d f o r 48 houre and the d i f f e r e n c e between a l l the s p e c t r a and the 48 hour s p e c t r a . The d i f f e r e n c e epectra enow the f o l l o w i n g f e a t u r e e : 1) There are l a r g e water peaks i n the c o a l pelleté which are l a r g e r than i n a KBr p e l l e t without c o a l . The s i z e o f the peak increases w i t h decreasing c o a l rank. 2) Drying f o r 48 houre s u b s t a n t i a l l y reducee the water absorptions a t 3450, 1640 and 600 cm" · Longer time s and higher temperatures produce l i t t l e a d d i t i o n a l change i n the e p e c t r a . 3) The d r y i n g a l e o reducee the peak i n t e n s i t i e s a t 1560 and 1360 cm" . 4) Drying producee no change i n the peak i n t e n s i t i e s a s s o c i a t e d w i t h a l i p h a t i c o r aromatic hydrogen. I t i e reasonable t o assume that the epectra obtained a f t e r 48 houre o f d r y i n g ( a t which p o i n t the epectra atop changing) are "moieture f r e e " i n the eame sense that c o a l d r i e d a t 110°C u n t i l i t etope l o o s i n g weight i e d e f i n e d to be "moieture f r e e " . The reeidue peak i n t e n s i t y c o n t r i b u t e d by the KBr i e t y p i c a l l y leee than 10% o f the i n t e n e i t y c o n t r i b u t e d by the c o a l (13). B e e r e Law To v e r i f y Beer β law, eamplee o f c o a l were prepared u s i n g approximately 0.5, 1.0 and 1.5 mg o f c o a l i n each 300 mg p e l l e t . To compare abeorbancee o f the eamplee i t i e neceeeary t o separate the e f f e c t o f the a b s o r p t i o n from t h a t o f s c a t t e r i n g caused by the c o a l p a r t i c l e e o r by imperfectione i n the KBr p e l l e t . E m p i r i c a l l y , t h i s s c a t t e r i n g can be represented reasonably w e l l by a s t r a i g h t l i n e . The appropriateness of t h i e

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

2

1

1

1

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

COAL AND COAL PRODUCTS

82

s t r a i g h t l i n e s c a t t e r i n g c o r r e c t i o n i s d i s c u s s e d i n (13)* To make the s c a t t e r i n g c o r r e c t i o n , a l i n e which i s tangent to the spectrum near 3800 and 2000 cm" i s s u b t r a c t e d from the spectrum over the r e g i o n i n which the base l i n e has p o s i t i v e values of absorbance. The s c a t t e r i n g c o r r e c t i o n was a p p l i e d to the s p e c t r a of the c o a l considered i n F i g . 1. The c o r r e c t e d s p e c t r a have a l s o been s c a l e d to 1 mg (DAF) per cm by m u l t i p l y i n g by 1

f

.

li

100 (100 - %ASH)



VT

. Wp/iW^

where A i s the p e l l e t a r e a , W , W and W are the weights i n mg of the c o a l sample, the for and the p e l l e t , and % ASH i s the weight percent ash determined by ASTM procedures. The r e s u l t s are presented i n F i g . 2. The s c a l e d s p e c t r a show some minor v a r i a t i o n s but i n general are reproduceable w i t h i n 5%. The most n o t i c e a b l e d i f f e r e n c e s are i n the KBr-H^O regions e s p e c i a l l y i n the .5 mg samples which, when s c a l e d , make the KBr-H^O more prominent. The near e q u a l i t y of the s p e c t r a f o r the three d i f f e r e n t sample weights i n d i c a t e s t h a t Beer's law a p p l i e s . E a r l i e r s t u d i e s reached the same c o n c l u s i o n (27, 29 - 31). Photoacoustic Spectroscopy A more recent measurement technique f o r the a n a l y s i s of f u e l s , p a r t i c u l a r l y s o l i d samples, i s the photoacoustic (PAS) measurement ( 3 2 ) . This technique allows IR s p e c t r a of s o l i d samples to be obtained e s s e n t i a l l y without p r e p a r a t i o n . PAS should be considered whenever p h y s i c a l sample p r e p a r a t i o n i s d i f f i c u l t or when an a r t i f a c t of p r e p a r a t i o n i s suspected to occur. The photoacoustic e f f e c t i n s o l i d s i n v o l v e s a thermal t r a n s f e r from the s o l i d sample to the surrounding gas. Energy absorbed from the IR r a d i a t i o n by the s o l i d heats the surface of the s o l i d , which i n t u r n c o n d u c t i v e l y heats a boundary l a y e r of gas next to the s o l i d s u r f a c e . Thus, sound i s generated at the frequency of the IR modulation and can be detected w i t h a microphone. This s i g n a l can be processed i n the same way as the modulated IR. Because of the d i f f e r e n t t r a n s f o r m a t i o n s i n the forme of the energy, the PAS s i g n a l s are much lower than i n d i r e c t IR a b s o r p t i o n measurements. Long data c o l l e c t i o n times a r e , therefore, required. D i f f u s e R e f l e c t a n c e Spectroscopy A t h i r d technique f o r the study of s o l i d s by FT-IR i s d i f f u s e r e f l e c t a n c e spectroscopy. The technique which was r e c e n t l y d e s c r i b e d by F u l l e r and G r i f f i t h s , (33, 34) a l l o w s good q u a l i t y s p e c t r a t o be obtained on neat powdered samples. The technique r e q u i r e s f i n e g r i n d i n g of the samples so, i n t h i s aspect, i t i s more r e s t r i c t i v e than PAS but i s s u b s t a n t i a l l y f a s t e r than PAS so i s a p p l i c a b l e to f o l l o w i n g reactions. F i g . 3 compares s p e c t r a f o r a P i t t s b u r g h seam c o a l ueing the three techniques. D i f f u s e r e f l e c t a n c e spectroscopy i s p a r t i c u l a r l y u s e f u l i n studying r e a c t i o n s where the KBr p e l l e t would r e s t r i c t access to the c o a l . As an example, c o n s i d e r the exchange of deuterium for RBr

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

+"W^)

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

SOLOMON E T A L .

Applications of FTIR

in Fuel Science

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

4.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

83

84

COAL AND COAL PRODUCTS

U)

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

Ο

UAVENUMBERS

Figure 3.

Spectra of a Pittsburgh seam coal by three techniques.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

4.

SOLOMON ET AL.

Applications of FTIR in Fuel Science

85

hydrogen on c o a l hydroxyl groups. This exchange may be accomplished i n a few minutes by exposing powdered c o a l t o D^O vapor. F i g * 4 shows the d i f f u s e r e f l e c t a n c e spectrum o f a d r i e d f i n e l y ground c o a l powder, the spectrum o f the same powder a f t e r exposure t o D^O vapor and then a f t e r exposure t o room a i r . The upper and lower s p e c t r a are almost i d e n t i c a l . The middle spectrum shows a decrease i n the OH r e g i o n (3400 wavenumbers) and an i n c r e a s e i n the OD r e g i o n (2600 wavenumbers). The s p e c t r a were obtained i n about two minutes, p e r m i t t i n g the k i n e t i c s o f the exchange t o be f o l l o w e d . Such deuterated c o a l samples have been used t o f o l l o w the chemical r e a c t i o n s o f the h y d r o x y l groups i n p y r o l y e i e by f o l l o w i n g the occurrence o f the deuterium i n the products (35). M i n e r a l A n a l y s i s and S p e c t r a l C o r r e c t i o n s The FT-IR s p e c t r a are obtained i n d i g i t a l form so t h a t c o r r e c t i o n s f o r p a r t i c l e s c a t t e r i n g and m i n e r a l content may be e a s i l y made. A typical c o r r e c t i o n sequence i s i l l u s t r a t e d i n F i g . 5. The upper curve i n F i g . 5 i s the uncorrected spectrum o f a d r i e d c o a l . I t has a slope from 1000 t o 4000 cm due t o p a r t i c l e s c a t t e r i n g and c o n t r i b u t i o n s from the m i n e r a l components near 3,600, 1,000 and 450 cm" . I d e n t i f i c a t i o n o f the minerals may be made by reference to s e v e r a l previous s t u d i e s (36 - 38). The bottom spectrum i n F i g . 5a has had the m i n e r a l peaks removed by s u b t r a c t i n g appropriate amounts o f the reference s p e c t r a shown i n F i g . 5b t o produce a smooth spectrum i n the r e g i o n o f the m i n e r a l peaks. S i m i l a r procedures f o r m i n e r a l a n a l y s i s using FT-IR have r e c e n t l y been reported by P a i n t e r e t a l . (7^, 8 ) . The spectrum a l s o has a s t r a i g h t l i n e s c a t t e r i n g c o r r e c t i o n and has been s c a l e d t o give the absorbance f o r 1 mg/cm^ o f dmmf c o a l . A more accurate way o f o b t a i n i n g the m i n e r a l components i s i l l u s t r a t e d i n F i g . 6 which i s the spectrum and m i n e r a l a n a l y s i s for the low temperature ash o f the c o a l i n F i g . 5. S p e c t r a l Synthesis Much previous work has been done t o i d e n t i f y the f u n c t i o n a l groups r e s p o n s i b l e f o r the observed peaks. Extensive references may be found i n Lowry, ( 1 ) , and van Krevelen (2). A convenient way t o o b t a i n areas under the absorbance peaks i s t o use a curve a n a l y s i s program t o s y n t h e s i z e the IR s p e c t r a (12). The s y n t h e s i s i s accomplished by adding a b s o r p t i o n peaks w i t h Gaussian o r L o r e n z i a n shapes and v a r i a b l e p o s i t i o n , w i d t h , and height as shown i n F i g . 7. The peaks are separated according to the i n d e n t i f i e d f u n c t i o n a l group. I t has been determined that most o f the f u e l r e l a t e d products which were s t u d i e d ( c o a l , t a r , char, o i l shale and t a r sand) could be synthesized by v a r y i n g only the magnitudes of a set o f peaks whose widths and p o s i t i o n s were h e l d constant. E x p e r i m e n t a l l y , the best shape f o r most o f the peaks i s a Gaussian. The f i t s obtained f o r s i x c o a l s o f v a r y i n g rank are i l l u s t r a t e d i n F i g . 8. The f i t s t o other products and model compounds are shown i n F i g . 9. For a t y p i c a l s i m u l a t i o n f o r c o a l s and chare the absolute value o f the area i n the d i f f e r e n c e between the spectrum and the s i m u l a t i o n i s t y p i c a l l y l e s s than 3% of the spectrum. For t a r s , r e c y c l e s o l v e n t s and o i l shales t h i s

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

COAL AND COAL PRODUCTS

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

86

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

SOLOMON ET AL.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

4.

40bo 36bo iibô

u

Applications of FTIR

iëbô

24 bo

in Fuel Science

2obo

i6bo

87

1200

(b)

υ ζ

Œ CD CC Ο

U) m ex

SYNTHES12ED SPECTRUM

M 1LL1TE 9.D'A 0URR72 2.5/. KR0L1N 3.1/. CRLC1TE

2.9/.

MONTMOR1LLRN1TE 1.2/ 40 BÔ

36b0

32b0

26b0

24 bO 20bû WRVENUMBERS

I6b0

12ÎD0

ebo

^ibo

Figure 5. Correction of coal spectrum for scattering and minerals. Key: a, correction of coal spectrum; b, determination of mineral spectrum by addition of reference spectra.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

COAL AND COAL PRODUCTS

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

88

Ρ5Η

οΑΐεο

Ζ α go

η α

ο

nONlnOBJLLPNllE 50.ΟΧ

ω

KPOLlN

m

0UART7

.or.

β.sr.

CALCHÉ 7.6*

lune 1. OK SObÔ

3 6 bO

F/gwre 6.

3200

2 ebO

2S00 2000 MAV£NUMB£A3

I et»

1200

ÏEÔÎ00

Synthesis of low temperature ash spectrum by addition of spectra from mineral library.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

SOLOMON ET AL.

Applications of FTIR

in Fuel Science

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

ο "

"1

WAVENUMBERS

Figure 7. Spectral synthesis of FTIR of Pittsburgh seam coal

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

COAL

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

COAL AND

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

PRODUCTS

ET

AL.

Applications of FTIR

in Fuel Science

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

SOLOMON

Figure 9.

Applications of spectral synthesis to other hydrocarbons.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

92

COAL AND

COAL

PRODUCTS

value i n c r e a s e s to 5% but was as h i g h as 14% i n one case. Optimum use of such a f i t t i n g procedure r e q u i r e s a set of c a l i b r a t i o n constants which r e l a t e s the d i s t r i b u t i o n of peaks i n the s y n t h e s i s to the a b e o r p t i v i t i e e of f u n c t i o n a l groups i n the sample. This i s the subject of a c o n t i n u i n g i n v e s t i g a t i o n . The Hydroxyl C o n c e n t r a t i o n The i n f r a r e d measurement of the h y d r o x y l c o n c e n t r a t i o n of c o a l s prepared i n KBr p e l l e t s was discussed by Osawa and Shih (27). These authors used the a b s o r p t i o n of the 0-H s t r e t c h at 3450 cm . Two major problems i n making t h i s determination are the o v e r l a p of a band due to water i n the c o a l or water absorbed i n preparing the KBr p e l l e t and s c a t t e r i n g which a l s o a f f e c t s t h i s r e g i o n of the spectrum. To overcome these problems Osawa and Shih d i d the f o l l o w i n g : 1) obtained s p e c t r a of c o a l i n KBr p e l l e t s a f t e r d r y i n g the p e l l e t s to reduce the water a b s o r p t i o n ; 2) obtained s p e c t r a at s e v e r a l sample s i z e s and determined "specific extinction coefficients" (more commonly c a l l e d a b s o r p t i v i t y ) from the slopes of absorbance V8 sample s i z e and 3) used a l i n e a r base l i n e c o r r e c t i o n f o r scattering. A p p l y i n g these techniques, they found a l i n e a r r e l a t i o n between the a b s o r p t i v i t y at 3450 cm and the h y d r o x y l content of the c o a l determined chemically. Many of Osawa and Shih'β suggestions were subsequently used i n measurements made by Solomon ( 1 2 ) . Painter and co-workers (26) have r e c e n t l y questioned s e v e r a l aspects of these procedures. For the h y d r o x y l determination these authors have suggested an a l t e r n a t i v e o r g i n a l l y used by Durie and S t e r n h e l l (29), which employs a c e t y l a t i o n of the c o a l and a n a l y s i s of the d i f f e r e n c e between s p e c t r a of raw and a c e t y l a t e d c o a l . This procedure has advantages i n a v o i d i n g the water problem and i n d i s t i n g u i s h i n g d i f f e r e n t types of OH groups but i s time consuming. The determination of hydroxyl d i r e c t l y from the absorbance i n the OH s t r e t c h r e g i o n would be much 8imp l i e r so i t i s worthwhile to evaluate i t s accuracy. This was done r e c e n t l y by Solomon and Carangelo (13). The r e s u l t s are summarized below. As seen i n the c o a l s p e c t r a the h y d r o x y l O-H s t r e t c h absorbance appears to be a broad band s t r e t c h i n g from 3600 to 2000 cm"* . The broadness of the band has been a t t r i b u t e d to hydrogen bonding. I t i s important to be sure that the band shape i s r e a l and not an a r t i f a c t of the s c a t t e r i n g c o r r e c t i o n . Several observations i n d i c a t e that the band shape i s r e a l . 1) S i m i l a r band shapes were observed by F r i e d e l and Queiser (39) u s i n g t h i n s e c t i o n s of c o a l which don't e x h i b i t s c a t t e r i n g and by Brown (4) using n u j o l m u l l s . 2) S i m i l a r band shapes are a l s o observed in non s c a t t e r i n g s p e c t r a of vacuum d i s t i l l e d c o a l t a r melted onto a KBr blank ( 1 2 ) . 3) Spectra f o r c o a l may a l s o be obtained by d i f f u s e r e f l e c t a n c e spectroscopy (33, 34) and by photoacoustic spectroscopy (32) which don't r e q u i r e KBr. Spectra of a P i t t s b u r g h seam c o a l taken u s i n g these methods are compared i n F i g . 3. A l l three s p e c t r a show the broad hydroxyl absorbance. 4) I t i s p o s s i b l e to change the shape of the h y d r o x y l absorbances by a l l o w i n g the hydrogen to exchange w i t h deuterium. This can be

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

4.

SOLOMON E T A L .

Applications of FTIR

93

in Fuel Science

done by exposing the c o a l t o D^O vapor. F i g . 4 shows the d i f f u s e r e f l e c t i o n spectrum of a dry c o a l and the c o a l a f t e r exposure f o r 1/2 hour t o D^O. The broad OH a b s o r p t i o n peak i s d r a s t i c a l l y reduced and the 0-D peak a t 2600 cm"" appears. 5) The broad peak i s a l s o d r a s t i c a l l y reduced by a c e t y l a t i o n (Durie and S t e r n h e l l (29)) and by a l k y l a t i o n ( L i o t a ( 4 0 ) ) . To v e r i f y that the broadness i n the peak i s due t o hydrogen bonding, s p e c t r a o f a t a r sample coated on a KBr p e l l e t were obtained a t e l e v a t e d temperatures (12). As expected f o r hydrogen bonding, the a b s o r p t i o n f o r bonded OH groups (3200 - 2400 c m ) decreases w h i l e that f o r f r e e OH i n c r e a s e s . The change i n the high temperature spectrum was not permanent as the room temperature spectrum returned a f t e r c o o l i n g . Osawa and Shih found a good l i n e a r r e l a t i o n s h i p between specific e x t i n c t i o n c o e f f i c i e n t s and h y d r o x y l c o n c e n t r a t i o n s determined u s i n g an a c e t y l a t i o n method. The c o r r e l a t i o n was e s p e c i a l l y good when c o n s i d e r i n g only Japanese c o a l s . I n the work of Solomon and Carangelo (13) the c o r r e l a t i o n was made using samples from the Pennsylvania State U n i v e r s i t y coal bank. Hydroxyl c o n c e n t r a t i o n s were determined c h e m i c a l l y by Yarzab, Abdel-Baset and Given ( 4 1 ) . The c o r r e l a t i o n was determined f o r the absorbance a t 3200 cm"* r a t h e r than 3450 used by Osawa and Shih (27) t o avoid problems of r e s i d u a l KBr water l e f t after drying. The broad OH absorbance i n c o a l has an i n t e n s i t y a t 3200 s i m i l a r t o that a t 3450 w h i l e the i n t e n s i t y due t o water i n KBr i s c l o s e t o zero. The absorbances a t 3200 cm f o r three c o a l s are p l o t t e d as f u n c t i o n s o f c o a l amount i n F i g . 10. The v a r i a t i o n of absorbance i s l i n e a r i n sample amount. The slope of the l i n e gives a(3200), the a b s o r p t i v i t y a t 3200 cm" i n ( a b s . units/cm /mg). The correlation of hydroxyl content and a b s o r p t i v i t y i s i l l u s t r a t e d i n F i g . 11. The h y d r o x y l content computed f o r 46 c o a l s u s i n g the c o r r e l a t i o n o f F i g . 11 i s i l l u s t r a t e d i n F i g . 12 as a f u n c t i o n o f carbon content. The data are f o r c o a l s from the Exxon c o a l sample bank which were analyzed r e c e n t l y . The Exxon c o a l s which were sealed i n n i t r o g e n when prepared were analyzed immediately w i t h i n dayβ a f t e r breaking the s e a l . Except f o r the c o a l s w i t h high h y d r o x y l content, the Exxon c o a l s appear t o l i e i n a t i g h t band which i s s l i g h t l y lower than the average values f o r the Penn State coals. The r e s u l t s a r e , however, d i f f e r e n t from the chemical determinations o f Osawa and Shih (27) and o f Blom (42). The r e s u l t s i n d i c a t e that h y d r o x y l oxygen c o n c e n t r a t i o n s i n c o a l can be determined by FT-IR w i t h an accuracy of about 10% compared t o the c h e m i c a l l y determined standards. The c o n s i s t e n c y of the chemical d e t e r m i n a t i o n o f OH should, however, be improved. A l i p h a t i c and Aromatic Hydrogen A c a l i b r a t i o n f o r the a l i p h a t i c peaks near 2900 cm and the aromatic peaks near 800 cm" was obtained by Solomon (12). The o b j e c t i v e was t o determine the values o f the i n t e g r a l a b s o r p t i v i t i e e a ' ( a l ) and a'(ar) ( i n abs. u n i t s cm /mg/cm ), which r e l a t e peak areas ( i n abs. u n i t s cm" ) t o the corresponding hydrogen c o n c e n t r a t i o n ( i n mg/cm ),

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

1

1

1

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

94

COAL AND COAL PRODUCTS

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

ΊΠ •ε . e

1.3 w a.

I~ |1 il il

i l

î" ο "g s: ο ο .

sa*

I-s

I

•-ι

S

3 .00

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

4.

Applications of FTIR

SOLOMON E T A L .

in Fuel Science

95

5

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

Ο ο CM σ

2

6

I*

OXYGEN IN OH (WT % DMMF) Figure 11.

Variation of absorptivity with hydroxyl concentration. (Reproduced, with permission, from Ref. 13.)

10 ι

11 osawa & shih ( 2 Z ) \

1

v

V

1

ι

-





blom (42 Κ

0

#

s

•yarzab(Ul)*s

\

U

i s χ D

-

CD

> -2 χ D 1 u

60

Figure 12.

65

1

1

70 75 CARBON

ι

ι

80 85 (WT. % DMMF)

ι \ Ν

90

95

Variation of hydroxyl concentration determined by FTIR with carbon concentration. (Reproduced, with permission, from Ref. 13.)

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

96

COAL

AND

COAL

PRODUCTS

A ( a l ) - a'(al) H(al) and A (ar)

» a'(ar) H(ar)

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

where A ( a l ) i s the area under the a l i p h a t i c peaks, A ( a r ) i s the area under the aromatic peaks and H ( a l ) and H(ar) the a l i p h a t i c (or hydroaromatic) and aromatic hydrogen c o n c e n t r a t i o n s i n the sample, r e s p e c t i v e l y . The equation for total hydrogen c o n c e n t r a t i o n H ( t o t a l ) » H ( a l ) + H(ar) + H(hydroxyl) may be combined w i t h the above equations to y i e l d , A(ar) A(al) L ! . 1 " a'(ar) H ( t o t a l ) - H(hydroxyl) »(al) H ( t o t a l ) - H(hydroxyl)) " where H(hydroxyl) i s the percent hydrogen i n h y d r o x y l groups. If a ' ( a l ) and a'(ar) are constant f o r a l l products than p l o t t i n g one term i n the square b r a c k e t s a g a i n s t the other should y i e l d a s t r a i g h t l i n e w i t h i n t e r c e p t s a ' ( a l ) and a ' ( a r ) . In Ref. (12) the above a n a l y s i s was performed f o r a group of c o a l s and model compounds. Peak areas were determined u s i n g a s p e c t r a l s y n t h e s i s r o u t i n e employing 26 Gaussian peaks as d e s c r i b e d above. Hydroxyl concentrations were determined from the i n f r a r e d s p e c t r a u s i n g the a b s o r p t i v i t y of Osawa and Shih ( 2 7 ) . The r e s u l t s i n d i c a t e a ' ( a l ) and a'(ar) to be constant f o r most c o a l products as w e l l as many model compounds c o n t a i n i n g aromatic r i n g s . Exceptions were long a l i p h a t i c c h a i n model compounds, and two h i g h a l i p h a t i c c o a l s and a low temperature t a r . For these samples, i t appears t h a t longer a l i p h a t i c chains r e s u l t i n a higher absorbance per hydrogen atom. The i n t e g r a l a b s o r p t i v i t i e s obtained were a ' ( a l ) - 900 and a'(ar) - 800 The above a n a l y s i s was a p p l i e d to a wider group of c o a l s ( i n c l u d i n g 44 c o a l s from the Exxon L i b r a r y and a number of c o a l s from the Pennsylvania S t a t e U n i v e r s i t y c o a l bank) and s e v e r a l s e t s of c h a r s , t a r s and r e c y c l e s o l v e n t s . S e v e r a l improvements were a l s o made i n the s p e c t r a l s y n t h e s i s r o u t i n e . The r e s u l t s are shown i n F i g . 13. F i g . 13a compares r e s u l t s f o r bituminous c o a l s and t h e i r chars and t a r s . For t h i s group of m a t e r i a l s the i n t e g r a l a b s o r p t i v i t i e s , determined from the r e g r e s s i o n a n a l y s i s are a ' ( a l ) - 746 a'(ar) - 686 F i g . 13b c o n t a i n s r e s u l t s f o r subbituminous c o a l s and l i g n i t e s and

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

SOLOMON ET

AL.

Applications of FTIR

in Fuel Science

97

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

4.

A(al)/(H(total) - H(hydroxyl))

Figure 13. Regression analysis to determine aromatic and aliphatic absorptivities. Key: a, bituminous coals and products; and b, lignite and subbituminous coals and products.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

98

COAL AND

COAL

PRODUCTS

t h e i r chars. The data l i e i n a band which i s lower than f o r the bituminous ( F i g . 13a) i n d i c a t i n g some v a r i a t i o n s i n a b s o r p t i v i t y w i t h rank. The i n t e g r a l a b s o r p t i v i t i e s are

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

a ' ( a l ) « 710 and a'(ar) « 541 The i n t e g r a l a b s o r p t i v i t i e s are lower than those p r e v i o u s l y obtained by Solomon (12) even though the bituminous group c o n t a i n s many of the c o a l s o r i g i n a l l y used. The major reason f o r the d i f f e r e n c e i s v a r i a t i o n s i n the choice of component peaks to use f o r the s p e c t r a l s y n t h e s i s . A p a r a l l e l problem i s the choice of i n t e g r a t i o n l i m i t s and the base l i n e when d i r e c t i n t e g r a t i o n i s used to o b t a i n peak areas. A l s o , the previous work contained o n l y one l i g n i t e and hydrogen v a l u e s were obtained on vacuum d r i e d samples by an elemental a n a l y z e r . These values were t y p i c a l l y lower than those obtained by ASTM procedures. In r e a n a l y z i n g these c o a l s the ASTM hydrogen values were used f o r c o n s i s t e n c y . In view of the p o s s i b l e v a r i a t i o n s i n a b s o r p t i v i t y w i t h the choice of peaks, i n t e g r a t i o n l i m i t s or base l i n e , i t i s e s s e n t i a l to use the same methods f o r determining peak areas f o r both the c a l i b r a t i o n of a b s o r p t i v i t i e s and the d e t e r m i n a t i o n of hydrogen concentrations· F i g . 14 compares values of H ( a l ) + H(ar) determined u s i n g the i n t e g r a l a b s o r p t i v i t i e s f o r the bituminous c o a l ( a ' i a l ) - 746 and a'(ar) » 686) and f o r the subbituminous c o a l s and l i g n i t e s ( a ' ( a l ) - 710 and a ( a r ) - 541 ) w i t h H ( t o t a l ) - H ( h y d r o x y l ) . The i n t e g r a l a b s o r p t i v i t i e s f o r a l i p h a t i c and aromatic hydrogen appear accurate f o r most c o a l s . As i n Ref. (12) exceptions are seen f o r some m a t e r i a l s w i t h h i g h a l i p h a t i c or hydroaromatic c o n c e n t r a t i o n s (above 4 to 5%). These i n c l u d e a l g i n i t e c o a l s , some t a r s , o i l s h a l e s , o i l s and c o a l l i q u e f a c t i o n recycle solvents. These compounds f a l l below the p a r i t y l i n e . The a l i p h a t i c l i n e shapes f o r these m a t e r i a l s appears to be higher and narrower and the a b s o r p t i v i t i e s are l a r g e r than those f o r most of the c o a l s and chars considered above. Model compounds containing long aliphatic chains or having extensive hydroaromatic i t y show s i m i l a r shapes and have s i m i l a r high a b s o r p t i v i t i e s (47). The aromatic hydrogen values computed, u s i n g the above a b s o r p t i v i t i e s , are i n agreement w i t h those f o r c o a l s of s i m i l a r rank determined by van K r e v e l e n (43) and by Mazumdar, et a l . (44) from p y r o l y s i s measurements but are l a r g e r (by about a f a c t o r of 2) than those determined by Brown (4) u s i n g IR techniques f o r the peaks near 3100 cm. Determination of Carbon F u n c t i o n a l Group Concentrations The c o n c e n t r a t i o n of aromatic and a l i p h a t i c carbons may be obtained u s i n g some simple assumptions. The s t o i c h i o m e t r y of the a l i p h a t i c p o r t i o n of the sample can be estimated and C(ar) can be c a l c u l a t e d using a method suggested by Brown and Ladner (14). The method determines C(ar) by d i f f e r e n c e . f

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

4.

Applications of FTIR

SOLOMON E T A L .

C(ar) « C ( t o t a l )

- C(total)

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

Where C ( t o t a l ) parameter which m a t e r i a l CH .

in Fuel Science

C(al)

(12/x) H ( a l )

i s the t o t a l carbon c o n c e n t r a t i o n and χ i s a d e s c r i b e s the s t o i c h i o m e t r y of the a l i p h a t i c The accuracy of the method has r e c e n t l y been

A

a

determined from H-NMR. For c o a l s , a v a l u e o f χ 1.8 i s reasonable. T h i s i s based on estimates o f the a l i p h a t i c s t o i c h i o m e t r y made by s e v e r a l i n v e s t i g a t o r s , a summary o f which appears i n Ref. ( 1 5 ) . Compari8ion w i t h NMR To check the accuracy o f the d e t e r m i n a t i o n o f aromatic and a l i p h a t i c carbons, eighteen c o a l s f o r which q u a n t i t a t i v e FT-IR data were obtained were a l s o studied by C NMR by Bernard G e r s t e i n e t a l . , (46) a t Ames Laboratory. The r a t i o s o f aromatic t o t o t a l carbon obtained by the two methods are compared i n F i g . 15. There i s good agreement between r e s u l t s of the two methods. Model Compounds A l i b r a r y of 156 model compounds o f i n t e r e s t i n c o a l has been created under EPRI and DOE sponsored programs (47, 4 8 ) . Q u a n t i t a t i v e FT-IR spectra were obtained i n d u p l i c a t e f o r each compound. The compounds which have known molecular s t r u c t u r e were used t o o b t a i n i n t e g r a l a b s o r p t i v i t i e s f o r f u n c t i o n a l groups of i n t e r e s t . In working w i t h c o a l and c o a l l i q u i d s which produce broad i n f r a r e d absorptions because o f t h e i r inhomogeneity, i t i s p r e f e r a b l e to work w i t h i n t e g r a t e d areas r a t h e r than peak h e i g h t s . For each compound, the i n t e g r a l a b s o r p t i v i t y a ' ( i ) i n Abs. u n i t s cm" /(mg/cm ) was determined which r e l a t e s the i n t e g r a t e d area A ( i ) i n absorbance u n i t s times wavenumber to the c o n c e n t r a t i o n of the absorbing species C ( i ) i n the sample i n mg/cm by the equation A(i)»

,

a (i)C(i)

Table I summarizes the absorbing groups and the r e g i o n s o f the spectrum considered and provides a summary o f the average i n t e g r a l a b s o r p t i v i t i e s w i t h 90% confidence l i m i t s . A number of conclusions may be drawn from these d a t a . A l i p h a t i c and Aromatic Hydrogen The average integral a b s o r p t i v i t i e s f o r H ( a l ) and H(ar) are a»(al) » 963 + 109

and a'(ar) » 768 + 85

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

100

COAL AND

H(al) + H(ar) by FTIR

COAL

PRODUCTS

(%)

Figure 14. Comparison of hydrogen concentrations determined chemically with those determined by FTIR. Key: Q, subbituminous coals, lignites, and products; and X, bituminous coals and products.

0

20

60

100

C /C - FTIR ar Figure 15.

Comparison of FTIR and NMR results for aromatic carbon.

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18

REGION H(al) H(ar) H(ar) WAG N-Hx O-C(al) O-C(ar) C-C a r Rng H-C ( s t r ) H2-C- s t r H3-C- s t r H3-C (wag) H-OO-C H-S- s t r «N- rng C(al)-C Ν other -S-

TITLE 2600 TO 3120 2600 TO 3120 665 TO 925 3140 TO 3600 NONE NONE NONE 2600 TO 3120 2600 TO 3120 2600 TO 3120 1360 TO 1400 NONE NONE 2500 TO 2600 NONE NONE NONE NONE

BASELINE LIMITS

2800 TO 3000 3000 TO 3120 680 TO 920 3140 TO 3600 1000 TO 1200 1160 TO 1320 1525 TO 1700 2800 TO 3000 2800 TO 3000 2800 TO 3000 1360 TO 1400 3200 TO 3600 1640 TO 1760 2500 TO 2600 NONE NONE NONE NONE

INTEGRATION LIMITS

963.189 242.693 768.354 7443.55 1078.05 1181.72 57.9966 9876.80 1338.76 3524.42 69.6250 22797.5 603.513 568.171

+/+/•/+/•/+/•/+/+/+/+/+/+/-

108.975 31.5441 85.9592 4793.54 266.587 285.379 17.0062 6586.99 188.994 1679.72 22.3508 3982.39 209.718

INTEGRAL ABSORPTIVITY

INTEGRATION LIMITS AND MEAN EXTINCTION COEFFICIENTS FOR ABSORBING GROUPS OF 156 MODEL COMPOUNDS

TABLE I

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

>

H

w

1

ι



2

2

2

6

In Coal and Coal Products: Analytical Characterization Techniques; Fuller, E.; ACS Symposium Series; American Chemical Society: Washington, DC, 1982.

2

110

COAL AND

Downloaded by UNIV LAVAL on July 16, 2014 | http://pubs.acs.org Publication Date: November 12, 1982 | doi: 10.1021/bk-1982-0205.ch004

1200 C.

COAL

PRODUCTS

.illiniuml u l l

Ο

ο

600 C 3«*bo

33bo

32bo

iïEo

23bo

11

s i bo''

sobo

29b0

28b0

22bo

2 i bo

2obo

Tibo

600 C. 25bo

4

u u o ζ in