15 Desulfurizing Coal with Alkaline Solutions Containing Dissolved Oxygen
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C. Y. TAI,* G. V. GRAVES, and T. D. WHEELOCK Iowa State University, Department of Chemical Engineering and Nuclear Engineering, Energy and Mineral Resources Research Institute, Ames, IA 50011 The extraction of pyritic sulfur from coal by leaching the comminuted material with hot aqueous solutions containing dissolved oxygen has been demonstrated in numerous laboratory experiments (1-6). Although acidic solutions have generally been used for such experiments, basic solutions appear to offer several important advantages. Thus Majima and Peters (7) showed that the rate of extraction of sulfur from relatively pure pyrite is much greater in basic solutions containing dissolved oxygen than in neutral solutions. Moreover it has been shown recently that basic solutions containing ammonium hydroxide and oxygen can extract a significant portion of the organic sulfur as well as most of the inorganic sulfur from coal at relatively moderate temperatures (e.g., 130°C) (4,5) whereas higher temperatures (150°-200°C) seem to be required with acidic solutions to remove organic sulfur (6). Furthermore some types of basic solutions are much less corrosive towards the common materials of construction than acidic solutions. A l t h o u g h the chemical kinetics and mechanism o f pyrite r e a c tion with an o x y g e n - b e a r i n g caustic solution have been studied, t h e y a r e n o t c o m p l e t e l y d e f i n e d . S t e n h o u s e and A r m s t r o n g ( 8 ) f o u n d s u l f a t e i o n s and i r o n o x i d e s t o be t h e f i n a l p r o d u c t s o f reaction. B o t h Fe2Û3 and Fe3Û4 were i d e n t i f i e d i n t h e r e s i d u e . I t a p p e a r e d t o t h e s e i n v e s t i g a t o r s t h a t t h e i r o n o x i d e s formed a s t a b l e l a y e r around t h e u n r e a c t e d p y r i t e . As a r e s u l t o f a l a t e r i n v e s t i g a t i o n , B u r k i n and Edward ( 9 ) c o n c l u d e d t h a t t h e f i n a l o x i d a t i o n p r o d u c t o f i r o n i s maghemite (yFe203) w h i c h i s formed t h r o u g h a s e r i e s o f t o p o t a c t i c t r a n s f o r m a t i o n s . These i n v e s t i g a t o r s o b s e r v e d t h a t t h e r a t e o f a t t a c k was more r a p i d a l o n g g r a i n b o u n d a r i e s and c r a c k s i n impure and i m p e r f e c t p y r i t e c r y s t a l s , w i t h t h e r e s u l t t h a t t h e s e p a r t i c l e s were l e a c h e d more r a p i d l y t h a n p a r t i c l e s c o n t a i n i n g few i m p e r f e c t i o n s and i m p u r i t i e s ,
*Present address: T a i w a n , R.O.C.
Chung-Shen I n s t i t u t e o f S c i e n c e and T e c h n o l o g y ,
182
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
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15.
TAi E T A L .
Alkaline
Solutions
with Dissolved
Oxygen
183
even though t h e i n s o l u b l e o x i d a t i o n p r o d u c t adhered t o t h e imper f e c t c r y s t a l s b u t n o t t o t h e p e r f e c t o n e s . As a r e s u l t o f t h e i n t e r g r a n u l a r a t t a c k by t h e l e a c h s o l u t i o n , t h e s m a l l e r c r y s t a l s w i t h i n p a r t i c l e s composed o f d i f f e r e n t - s i z e d c r y s t a l s were d e s u l f u r i z e d b e f o r e t h e l a r g e r c r y s t a l s . The r e a c t i o n r a t e i n c r e a s e d w i t h temperature a c c o r d i n g t o the A r r h e n i u s e q u a t i o n w i t h an a c t i v a t i o n energy o f 9 k c a l / m o l . A l s o t h e r e a c t i o n r a t e was c o n t o l l e d by t h e o x y g e n c o n c e n t r a t i o n a t t h e m i n e r a l - s o l u t i o n i n t e r face so t h e r a t e i n c r e a s e d w i t h the oxygen p a r t i a l p r e s s u r e . In a d d i t i o n , the r a t e increased with i n c r e a s i n g concentration o f s o d i u m h y d r o x i d e up t o 2 wt %. H i g h e r c o n c e n t r a t i o n s r e d u c e d t h e rate s l i g h t l y . I n a s o l u t i o n o f some b a s e s u c h a s s o d i u m h y d r o x i d e , t h e s t o i c h i o m e t r y o f t h e r e a c t i o n o f p y r i t e w i t h o x y g e n and t h e s u b s e q u e n t n e u t r a l i z a t i o n o f t h e a c i d p r o d u c e d c a n p r o b a b l y be r e p r e s e n t e d by t h e f o l l o w i n g e q u a t i o n s : FeS
2
+ ^| 0
2
+ 2 H 0 = y F e ^ + 2 H SC> 2
2
4
2 H S 0 . + 4 NaOH = 2 N a S 0 , + 4 H 0 2 4 2 4 2 o
o
o
(1) (2)
A l t h o u g h these e q u a t i o n s s u g g e s t t h a t the main purpose o f t h e a l k a l i i s t o n e u t r a l i z e t h e a c i d and t o d r i v e t h e f i r s t r e a c t i o n t o c o m p l e t i o n , t h e a c t u a l r e a c t i o n mechanism i s p r o b a b l y more c o m p l e x w i t h t h e a l k a l i p l a y i n g a more s u b t l e r o l e a s w e l l a s t h e o b v i o u s one. An i n v e s t i g a t i o n by McKay a n d H a l p e r n ( 1 0 ) o f t h e r e a c t i o n o f p y r i t e w i t h o x y g e n i n a c i d i c s o l u t i o n s showed t h a t t h e p r o d u c t d i s t r i b u t i o n , and t h e r e f o r e t h e r e a c t i o n mechanism, i s q u i t e d i f f e r e n t f r o m t h a t n o t e d above f o r b a s i c s o l u t i o n s . Thus p y r i t e was c o n v e r t e d t o s o l u b l e f e r r o u s and f e r r i c s u l f a t e , s u l f u r i c a c i d , and e l e m e n t a l s u l f u r when l e a c h e d w i t h o x y g e n - b e a r i n g a c i d i c s o l u t i o n s a t 100°-130°C. The p r o d u c t d i s t r i b u t i o n depended on t e m p e r a t u r e a n d a c i d i t y , w i t h a l o w e r t e m p e r a t u r e and h i g h e r a c i d i t y f a v o r i n g t h e p r o d u c t i o n o f e l e m e n t a l s u l f u r a n d a h i g h e r tem p e r a t u r e and l o w e r a c i d i t y f a v o r i n g t h e p r o d u c t i o n o f s u l f u r i c a c i d and s o l u b l e s u l f a t e s . A l s o a t m o d e r a t e pH ( b u t n o t a t l o w ρΗ), t h e f e r r i c h y d r o x i d e h y d r o l y z e d , and f e r r i c o x i d e p r e c i p i tated. The A r r h e n i u s a c t i v a t i o n e n e r g y was d e t e r m i n e d t o be 13 k c a l / m o l , w h i c h , b e i n g s i g n i f i c a n t l y l a r g e r t h a n t h a t n o t e d above for the reaction of p y r i t e i na caustic s o l u t i o n , indicates a g r e a t e r e n e r g y b a r r i e r f o r t h e r e a c t i o n i n a n a c i d i c medium. The p r e s e n t i n v e s t i g a t i o n was u n d e r t a k e n t o e v a l u a t e t h e t e c h n i c a l f e a s i b i l i t y o f e x t r a c t i n g s u l f u r from c o a l w i t h h o t oxygen-bearing s o l u t i o n s . S i n c e i t was s o o n c o n f i r m e d t h a t a l k a l i n e o r b a s i c s o l u t i o n s r e s u l t e d i n a much g r e a t e r r a t e o f e x t r a c t i o n t h a n a c i d i c s o l u t i o n s , c o n s i d e r a b l e e m p h a s i s was p l a c e d on d e t e r m i n i n g t h e e f f e c t i v e n e s s o f d i f f e r e n t a l k a l i s a n d a l k a l i concentrations. Several h i g h - s u l f u r bituminous c o a l s , as w e l l as
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
184
COAL
DESULFURIZATION
p y r i t e w h i c h had been i s o l a t e d f r o m one o f t h e s e c o a l s , were l e a c h e d i n a s m a l l s t i r r e d r e a c t o r under a v a r i e t y of e x p e r i mental c o n d i t i o n s . In a d d i t i o n the o v e r - a l l e f f e c t i v e n e s s of c h e m i c a l l e a c h i n g i n c o m b i n a t i o n w i t h p h y s i c a l b e n e f i c i a t i o n was investigated.
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Experimental L e a c h i n g e x p e r i m e n t s were c a r r i e d o u t i n a 1-L, s t a i n l e s s s t e e l a u t o c l a v e e q u i p p e d w i t h a r e m o v a b l e n i c k e l l i n e r and an a g i t a t o r c o n s i s t i n g o f two p i t c h e d b l a d e t u r b i n e i m p e l l e r s (7.3 cm d i a m e t e r ) mounted on a s h a f t d r i v e n by a c o m p r e s s e d a i r m o t o r . The a u t o c l a v e was a l s o e q u i p p e d w i t h a p r e s s u r e gauge, t e m p e r a t u r e i n d i c a t o r , and e l e c t r i c h e a t i n g j a c k e t . A s u s p e n s i o n o f c o a l o r p y r i t e p a r t i c l e s i n an a l k a l i n e s o l u t i o n o f a s p e c i f i c c o n c e n t r a t i o n was p l a c e d i n t h e r e a c t o r w h i c h was t h e n s e a l e d and h e a t e d t o a s p e c i f i c o p e r a t i n g t e m p e r a ture. A f t e r t h e s y s t e m a t t a i n e d t h i s t e m p e r a t u r e , o x y g e n was introduced f r o m a h i g h - p r e s s u r e c y l i n d e r e q u i p p e d w i t h a comb i n a t i o n p r e s s u r e - r e d u c i n g v a l v e and r e g u l a t o r . D u r i n g t h e s u c c e e d i n g o p e r a t i o n , t h e s y s t e m p r e s s u r e was k e p t c o n s t a n t by s u p p l y i n g o x y g e n on demand. A l s o a s m a l l amount o f gas was b l e d c o n t i n u o u s l y f r o m t h e r e a c t o r t o a v o i d any b u i l d - u p o f g a s e o u s r e a c t i o n p r o d u c t s i n the s y s t e m . R e a c t i o n c o n d i t i o n s were k e p t c o n s t a n t f o r a s p e c i f i c t i m e w h i l e t h e m a t e r i a l was l e a c h e d . At t h e end o f t h e r e a c t i o n p e r i o d , the f l o w o f o x y g e n i n t o t h e s y s t e m was s t o p p e d , and t h e s y s t e m was c o o l e d . Throughout the o p e r a t i o n t h e a g i t a t o r was k e p t r u n n i n g a t a c o n s t a n t speed w h i c h was u s u a l l y i n the r a n g e o f 250-350 rpm. A f t e r a run the l e a c h e d s o l i d s were r e c o v e r e d , d r i e d , and w e i g h e d . C o a l s a m p l e s w e r e a n a l y z e d by t h e s t a n d a r d ASTM methods o f a n a l y s i s ( 1 1 ) . When p y r i t e a l o n e was l e a c h e d , t h e amount o f s u l f u r e x t r a c t e d was d e t e r m i n e d by m e a s u r i n g t h e s u l f a t e c o n t e n t o f t h e s p e n t l e a c h a n t u s i n g t h e s u l f a t e t i t r a t i o n method o f F r i t z and Yamaraura ( 1 2 ) . C o a l s a m p l e s f r o m t h e B i g Ben, ICO, and ISU Demonstration M i n e No. 1, a l l l o c a t e d i n S o u t h e a s t e r n Iowa, were l e a c h e d . The rank of the c o a l from these mines i s h i g h v o l a t i l e C b i t u m i n o u s c o a l ; t y p i c a l c o m p o s i t i o n s a r e shown i n T a b l e I . S i n c e t h e c o a l from these mines i s v e r y heterogeneous, v a r i o u s batches used f o r s p e c i f i c s e t s o f e x p e r i m e n t s were r e - a n a l y z e d and the c o m p o s i t i o n reported along with other experimental r e s u l t s . A h a n d p i c k e d sample o f i r o n p y r i t e s was o b t a i n e d f r o m t h e c o a l d e p o s i t a t ISU D e m o n s t r a t i o n M i n e No. 1. T h i s m a t e r i a l was v e r y i m p u r e and seemed t o c o n t a i n a b o u t 74% FeS2» Nevertheless, i t was g r o u n d and s c r e e n e d i n t o v a r i o u s s i z e d f r a c t i o n s w h i c h were u s e d s u b s e q u e n t l y f o r v a r i o u s l e a c h i n g e x p e r i m e n t s . The s u l f u r c o n t e n t o f t h e d i f f e r e n t s i z e f r a c t i o n s i s shown i n T a b l e II. I n a d d i t i o n t o p y r i t i c s u l f u r , t h e m a t e r i a l c o n t a i n e d some s u l f u r i n t h e f o r m o f s u l f a t e s and some i n a f o r m w h i c h was n e i t h e r p y r i t i c nor s u l f a t e .
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
15.
TAi E T A L .
Alkaline
Solutions
with Dissolved
185
Oxygen
T a b l e I . P r o x i m a t e A n a l y s i s o f Iowa C o a l s
Proximate A n a l y s i s
Source o f C o a l
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Big
Ben mine
Volatile Matter
Fixed Carbon
(wt %)
Ash
Moisture
37.5
48.8
1.2
12.5
ICO mine
44.0
42.0
4.5
9.5
ISU mine
38.1
44.2
2.2
15.5
Table I I .
Composition of Iron
Pyrites
Composition Size Fraction (U.S. S e r i e s Mesh)
Iron
Pyritic Sulfur
Sulfate Sulfur
(wt %) Total Sulfur
41.7
-60/+80 39.,2
0.,5
40.9
-200/+230
36.,4
0.,7
40.3
-230/+270
36.,3
0..7
39.4
-120/+140
Other
42.5
16.6
P y r i t e Leaching Experiments A s e r i e s o f l e a c h i n g e x p e r i m e n t s was c a r r i e d o u t t o d e t e r mine t h e e f f e c t o f v a r i o u s s y s t e m p a r a m e t e r s on t h e e x t r a c t i o n o f s u l f u r f r o m impure p y r i t e . F o r each experiment a s u s p e n s i o n cons i s t i n g o f 2.0 g o f p y r i t e p a r t i c l e s and 500 m l o f a n aqueous s o l u t i o n was t r e a t e d i n t h e s t i r r e d a u t o c l a v e a t 150°C w i t h o x y g e n d i s s o l v e d under a p a r t i a l p r e s s u r e o f 3.27 atm. S i n c e t h e v a p o r p r e s s u r e o f w a t e r a t t h i s t e m p e r a t u r e i s 4.56 atm, t h e t o t a l s y s t e m p r e s s u r e was 7.8 atm. U n l e s s i n d i c a t e d o t h e r w i s e , t h e l e a c h i n g o p e r a t i o n under o x y g e n p r e s s u r e a t t h e s p e c i f i e d t e m p e r a t u r e was c o n d u c t e d f o r 1 h r . The c o n v e r s i o n o f a l l forms o f s u l f u r i n t h e p a r t i c l e s t o s o l u b l e s u l f a t e was d e t e r m i n e d by a n a l y z ing the spent l e a c h a n t . The r e s u l t s p r e s e n t e d i n F i g u r e 1 i n d i c a t e t h a t among t h e v a r i o u s a l k a l i s t e s t e d , s o d i u m c a r b o n a t e was t h e most e f f e c t i v e . E s s e n t i a l l y a l l o f t h e s u l f u r was e x t r a c t e d f r o m -200/+230 mesh
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
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186
C O A L DESULFURIZATION
p y r i t e p a r t i c l e s i n 1.0 h r by an o x y g e n a t e d s o l u t i o n c o n t a i n i n g 1.5 wt % s o d i u m c a r b o n a t e . The b e s t r e s u l t s o b t a i n e d w i t h e i t h e r s o d i u m h y d r o x i d e o r s o d i u m p h o s p h a t e were s l i g h t l y l e s s f a v o r a b l e and w i t h ammonium c a r b o n a t e much l e s s f a v o r a b l e . The ammonium c a r b o n a t e s o l u t i o n s were n o t i c e a b l y l e s s b a s i c t h a n t h e o t h e r s o l u t i o n s and t h i s f a c t o r p r o b a b l y a c c o u n t e d f o r t h e p o o r e r r e s u l t s o b t a i n e d w i t h them. However, t h e ammonium c a r b o n a t e s o l u t i o n s , as w e l l as t h e o t h e r a l k a l i n e s o l u t i o n s , a l l gave b e t t e r r e s u l t s t h a n w a t e r and o x y g e n a l o n e . Thus o n l y 27% o f the s u l f u r was e x t r a c t e d f r o m t h e p y r i t e d u r i n g a r u n made w i t h o u t any alkali. The e f f e c t i v e n e s s o f a l l o f the a l k a l i s i n c r e a s e d w i t h i n i t i a l c o n c e n t r a t i o n up t o some optimum v a l u e and t h e n d e c r e a s e d . F o r s o d i u m h y d r o x i d e t h e optimum i n i t i a l c o n c e n t r a t i o n was a b o u t 1 wt %, f o r s o d i u m c a r b o n a t e 1.5 wt %, f o r s o d i u m p h o s p h a t e 3 wt %, and f o r ammonium c a r b o n a t e 4 wt %. The s h a r p i n c r e a s e i n c o n v e r s i o n f o r i n i t i a l c o n c e n t r a t i o n s a t the low end o f the c o n c e n t r a t i o n s c a l e seems t o be r e l a t e d t o t h e amount o f a l k a l i r e q u i r e d to n e u t r a l i z e a l l of the a c i d produced i n o x i d i z i n g the pyrite. Thus i f i t i s assumed t h a t a l l o f the s u l f u r i n t h e s o l i d s was c o n v e r t e d i n t o s u l f u r i c a c i d d u r i n g t h e l e a c h i n g o p e r a t i o n , i t w o u l d have r e q u i r e d an i n i t i a l s o d i u m h y d r o x i d e c o n c e n t r a t i o n o f 0.40 wt % t o n e u t r a l i z e a l l o f t h e a c i d p r o duced. I n t e r e s t i n g l y enough, t h e d a t a p r e s e n t e d i n F i g u r e 1 show t h a t t h e c o n v e r s i o n f e l l o f f s h a r p l y when l e s s t h a n 0.40 wt % c a u s t i c was u s e d . The amount o f s o d i u m c a r b o n a t e r e q u i r e d t o n e u t r a l i z e t h e a c i d depends on t h e f i n a l p r o d u c t s o f n e u t r a l i z a t i o n . Two p o s s i b i l i t i e s a r e shown b e l o w . H S0. + N a C 0 2 4 2 3 o
o
o
= Na S0. + C0 + H 0 2 4 2 2 o
o
(3)
o
H S 0 . + 2 N a C 0 = N a S 0 . + 2 NaHC0 2 4 2 3 2 4 3 o
o
o
o
o
(4)
The f i r s t r e a c t i o n w o u l d have r e q u i r e d an i n i t i a l s o d i u m c a r b o n a t e c o n c e n t r a t i o n o f 0.53 wt % t o n e u t r a l i z e a l l o f t h e s u l f u r i c a c i d w h e r e a s t h e s e c o n d r e a c t i o n w o u l d have r e q u i r e d an i n i t i a l c o n c e n t r a t i o n o f 1.1 wt %. The e x p e r i m e n t a l r e s u l t s ( F i g u r e 1) i n d i c a t e t h a t t h e c o n v e r s i o n f e l l o f f s h a r p l y when l e s s t h a n a b o u t 1 wt % s o d i u m c a r b o n a t e was u s e d . I n t h e c a s e o f s o d i u m p h o s p h a t e an i n i t i a l c o n c e n t r a t i o n o f 1.65 wt % w o u l d have been r e q u i r e d t o n e u t r a l i z e a l l o f the p o s s i b l e s u l f u r i c a c i d a c c o r d i n g to the f o l l o w i n g r e a c t i o n : H S 0 . + 2 N a P 0 . = N a S 0 . + 2 Na HP0. 2 4 3 4 2 4 2 4 o
o
o
o
(5)
A l t h o u g h the e x p e r i m e n t a l r e s u l t s shown i n F i g u r e 1 i n d i c a t e t h a t the c o n v e r s i o n f e l l o f f s h a r p l y between 2 and 3 wt %, the s p a r s i t y o f t h e d a t a l e a v e c o n s i d e r a b l e d o u b t as t o the e x a c t c r i t i c a l
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
Downloaded by UNIV LAVAL on June 28, 2014 | http://pubs.acs.org Publication Date: June 1, 1977 | doi: 10.1021/bk-1977-0064.ch015
15.
TAI E T A L .
Alkaline
Solutions
with Dissolved
Oxygen
187
concentration. Why t h e c o n v e r s i o n d e c l i n e d a t h i g h e r a l k a l i c o n c e n t r a t i o n s w h i c h e x c e e d e d t h e optimum l e v e l s c a n n o t be e x p l a i n e d w i t h c e r tainty. A s i m i l a r d e c l i n e was o b s e r v e d by B u r k i n and Edwards ( 9 ) when p y r i t e was l e a c h e d w i t h c a u s t i c s o l u t i o n s , a n d t h e y a t t r i b u t ed t h e d e c l i n e t o the r e d u c e d s o l u b i l i t y o f o x y g e n i n t h e s e s o l u tions. A l s o s i m i l a r b e h a v i o r was o b s e r v e d i n l e a c h i n g b o t h g a l e n a and m o l y b d e n i t e w i t h c a u s t i c s o l u t i o n s c o n t a i n i n g d i s s o l v e d o x y g e n (13,14). I n the case o f both m i n e r a l s , a d e c l i n e i n r e a c t i o n r a t e w i t h i n c r e a s i n g a l k a l i c o n c e n t r a t i o n was a t t r i b u t e d t o t h e d e c r e a s i n g s o l u b i l i t y o f oxygen. The r e s u l t s o f l e a c h i n g d i f f e r e n t s i z e d f r a c t i o n s o f p y r i t e w i t h sodium carbonate s o l u t i o n s o f d i f f e r e n t c o n c e n t r a t i o n s a r e p r e s e n t e d i n F i g u r e 2. C l e a r l y t h e e f f e c t o f p a r t i c l e s i z e o n c o n v e r s i o n was v e r y p r o n o u n c e d w i t h t h e c o n v e r s i o n i n c r e a s i n g i n an a l m o s t e x p o n e n t i a l manner a s t h e s i z e was r e d u c e d ( F i g u r e 2 ) . P a r t i c l e s s m a l l e r t h a n 60 ym i n d i a m e t e r were c o m p l e t e l y d e s u l f u r i z e d i n 1.0 h r by s o l u t i o n s c o n t a i n i n g 2-5 wt % s o d i u m c a r b o n a t e f o r t h e c o n d i t i o n s shown i n F i g u r e 2. On t h e o t h e r h a n d , p a r t i c l e s l a r g e r t h a n 210 ym i n d i a m e t e r were o n l y a b o u t h a l f d e s u l f u r i z e d u n d e r t h e s e c o n d i t i o n s . F i g u r e 2 a l s o shows t h e advantage o f u s i n g an a l k a l i n e s o l u t i o n . The l o w e r c u r v e i n t h i s d i a g r a m r e p r e s e n t e d t h e c o n v e r s i o n o b t a i n e d when no a l k a l i was added t o t h e s y s t e m . Even w i t h t h e s m a l l e s t p a r t i c l e s o f p y r i t e , o n l y 3 5 % o f t h e s u l f u r was e x t r a c t e d i n the a b s e n c e o f a n a l k a l i . S e v e r a l r u n s were made u s i n g l o n g e r r e a c t i o n t i m e s t o s e e how the c o n v e r s i o n w o u l d change w i t h t i m e ( F i g u r e 3 ) . The r e s u l t s i n d i c a t e t h a t t h e r e a c t i o n r a t e d e c r e a s e d a s the b a t c h l e a c h i n g o p e r a t i o n p r o c e e d e d . The d e c l i n i n g r a t e c o u l d have been c a u s e d by t h e d e c r e a s i n g a v a i l a b i l i t y o f u n r e a c t e d p y r i t e , i n c r e a s i n g resistance to diffusion of reactants within p a r t i c l e s , increasing c o n c e n t r a t i o n o f some r a t e - i n h i b i t i n g r e a c t i o n p r o d u c t i n t h e l e a c h s o l u t i o n , o r a combination o f these f a c t o r s . Coal Leaching
Experiments
A s e r i e s o f l e a c h i n g e x p e r i m e n t s was c a r r i e d o u t t o d e t e r mine t h e e f f e c t s o f v a r i o u s a l k a l i s and a l k a l i c o n c e n t r a t i o n s on t h e d e s u l f u r i z a t i o n o f c o a l f r o m t h e I S U D e m o n s t r a t i o n M i n e No. 1. The raw c o a l was p u l v e r i z e d s o t h a t 9 0 % was f i n e r t h a n 200 mesh. F o r e a c h e x p e r i m e n t 50 g o f c o a l and 500 ml o f w a t e r o r a l k a l i n e s o l u t i o n were p l a c e d i n t h e s t i r r e d a u t o c l a v e . The c h e m i c a l t r e a t m e n t was c a r r i e d o u t f o r 2 h r a t 150°C w i t h o x y g e n d i s s o l v e d u n d e r a p a r t i a l p r e s s u r e o f 3.27 atm and u s i n g a t o t a l s y s t e m p r e s s u r e o f 7.8 atm. The t r e a t e d c o a l was r e c o v e r e d , d r i e d , w e i g h e d , and a n a l y z e d t o d e t e r m i n e t h e e f f e c t i v e n e s s o f t h e t r e a t ment . The b e s t o v e r a l l r e s u l t s were o b t a i n e d w i t h s o d i u m c a r b o n a t e among t h e f o l l o w i n g a l k a l i s w h i c h were t e s t e d i n v a r i o u s c o n c e n trations: sodium carbonate, sodium h y d r o x i d e , sodium phosphate,
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
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188
COAL DESULFURIZATION
PYRITE -200/+23O MESH 7.8 atm. TOTAL PRESS. 150 °C 1.0 h r .
Figure 1. The effect of different alkalis and alkali concentrations on the extraction of sulfur from pyrite
Figure 2. The effect of particle size on the extraction of sulfur from pyrite
J 2
4
L
6
8
10
INITIAL CONCENTRATION, wt. %
100
150
200
PYRITE PARTICLE SIZE, microns
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
250
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15.
TAI E T A L .
Alkaline
Solutions
with Dissolved
Oxygen
189
c a l c i u m c a r b o n a t e , c a l c i u m h y d r o x i d e , and ammonium c a r b o n a t e . The o n l y a l k a l i w h i c h a p p r o a c h e d s o d i u m c a r b o n a t e i n e f f e c t i v e n e s s was s o d i u m p h o s p h a t e . However, i t r e q u i r e d a 7 wt % i n i t i a l c o n c e n t r a t i o n o f sodium phosphate t o produce c o a l w i t h a s u l f u r c o n t e n t c o m p a r a b l e t o t h a t o b t a i n e d w i t h a 1.4 wt % i n i t i a l c o n c e n t r a t i o n of sodium carbonate. M o r e o v e r , t h e B t u r e c o v e r y was l o w e r and t h e a s h c o n t e n t o f t h e p r o d u c t h i g h e r when s o d i u m p h o s p h a t e was used to o b t a i n c o m p a r a b l e d e s u l f u r i z a t i o n . The i n i t i a l c o n c e n t r a t i o n o f s o d i u m c a r b o n a t e had a v e r y p r o nounced e f f e c t on t h e e x t e n t o f d e s u l f u r i z a t i o n and t h e r e s u l t i n g s u l f u r c o n t e n t o f t h e t r e a t e d c o a l ( T a b l e I I I , F i g u r e 4 ) . The b e s t r e s u l t s were o b t a i n e d w i t h an i n i t i a l c o n c e n t r a t i o n o f 1.4 wt % and u s i n g e i t h e r l o w e r o r h i g h e r c o n c e n t r a t i o n s r e s u l t e d i n l e s s desulfurization. The t r e a t m e n t w i t h t h e optimum c o n c e n t r a t i o n r e duced t h e p y r i t i c s u l f u r c o n t e n t o f t h e c o a l by t w o - t h i r d s . A s i m i l a r e f f e c t o f c o n c e n t r a t i o n was o b s e r v e d when s o d i u m h y d r o x i d e was u s e d w i t h the optimum i n i t i a l c o n c e n t r a t i o n b e i n g a b o u t 1 wt %. Hence, t h e e f f e c t o f a l k a l i c o n c e n t r a t i o n was l i k e t h a t e x p e r i e n c e d in leaching pyrite (Figure 1 ) . Under t h e m i l d l e a c h i n g c o n d i t i o n s used i n t h i s w o r k , m a i n l y i n o r g a n i c s u l f u r was e x t r a c t e d f r o m t h e c o a l . Essentially a l l o f t h e s u l f a t e f o r m o f s u l f u r was e x t r a c t e d a n d a good s h a r e o f the p y r i t i c s u l f u r . Unfortunately the r e s u l t s reported i n Table I I I f o r o r g a n i c s u l f u r a r e so e r r a t i c t h a t i t i s n o t p o s s i b l e t o d i s c e r n w h e t h e r o r g a n i c s u l f u r was removed o r n o t . For the e x p e r i m e n t s i n v o l v i n g sodium c a r b o n a t e , the y i e l d o f d r y c o a l was 93-94%, and t h e B t u r e c o v e r y was 88-92%. These v a l u e s c o u l d have been h i g h e r w i t h t h e e x e r c i s e o f g r e a t e r c a r e in conducting the experiments. Since the heating value o f the t r e a t e d c o a l on a m o i s t u r e and a s h f r e e (maf) b a s i s was n e a r l y t h e same as t h a t o f t h e u n t r e a t e d c o a l , i t does n o t a p p e a r t h a t t h e c o a l was s i g n i f i c a n t l y d e g r a d e d by t h e t r e a t m e n t . A l s o the oxygen c o n t e n t o f t h e c o a l , a s d e t e r m i n e d by u l t i m a t e c h e m i c a l a n a l y s i s , d i d n o t a p p e a r t o be s i g n i f i c a n t l y d i f f e r e n t f r o m t h a t o f t h e untreated coal. These r e s u l t s c o n t r a s t m a r k e d l y w i t h t h o s e r e p o r t e d b y S a r e e n e t a l . ( 3 , 4 ) f o r t r e a t m e n t s u s i n g much h i g h e r oxygen p a r t i a l p r e s s u r e s which r e s u l t e d i n n o t i c e a b l e oxygen upt a k e by I l l i n o i s No. 6 c o a l . As a r e s u l t o f t h e a l k a l i t r e a t m e n t , t h e s o d i u m and a s h c o n t e n t o f t h e c o a l i n c r e a s e d m e a s u r a b l y ( T a b l e I I I , F i g u r e 5 ) . The i n c r e a s e i n a s h c o n t e n t was d i r e c t l y p r o p o r t i o n a l t o t h e i n c r e a s e i n s o d i u m c o n t e n t and seemed c a u s e d a l m o s t e n t i r e l y by t h e a d s o r p t i o n o f s o d i u m . Most o f t h e i n c r e a s e i n s o d i u m o r a s h c o n t e n t t o o k p l a c e a t l o w e r a l k a l i c o n c e n t r a t i o n s , and more t h a n 2 wt % sodium carbonate i n t h e l e a c h a n t g e n e r a l l y produced l i t t l e a d d i tional increase. I n o t h e r w o r d s , t h e c o a l seemed t o become s a t u r a t e d when t h e l e a c h s o l u t i o n c o n t a i n e d 2 wt % s o d i u m c a r b o n a t e o r more. On t h e o t h e r hand, t h e c o a l r e t a i n e d v e r y l i t t l e s o d i u m when t h e l e a c h s o l u t i o n i n i t i a l l y c o n t a i n e d 0.8 wt % s o d ium c a r b o n a t e o r l e s s b e c a u s e t h e s o l u t i o n became a c i d i c b y t h e
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
92
91
93
93
94
94
94
2.0
5.0
8.0
10.0
15.0
chemical
chemical
chemical
chemical
89
90
88
11,010
10,940
10,950
10,590
10,880
10,580
10,780
18.5 19.4 19.7 18.2
— — —
17.8
17.7
13,800
13,520
13,520
16.4
chemical
91
89
—
93
1.4
93
1.0
chemical
10,740
16.3
chemical
90
—
94
0.8
16.2
13,430
chemical
10,950
94
0.8
chemical
92
17.5
—
10,440
88
0
chemical
95
15.3
15.5
13,970
13,660
maf
1.52
1.90
—
1.29
1.14
0.80
0.33
0.10
0.10
—
0.03
0.05
Ash Na ( w t . % ) (wt %)
11,577
as r e e v d .
Heat Value ( B t u / l b )
wash
Btu Recov. (%) 11,240
Wt Yield (%)
none
Treatment
Na2CC>3 Cone. (wt %)
0.17
3.,21
2.,34
1.,63
1.,76
1.,75
1.,23
1.,11
1.,46
1.,89
1.,62
0.18
0.11
0.09
0.11
0.07
0.06
0.05
0.03
0.05
0.11
0.60
2.,28
(lb/10
6
Btu)
3.66 1.80
2.65
2.28
5.17
4.02
4.24
3.15
1.85
2.39
2.99
3.90 1.81
2.39
4.23
3.47
1.80 2.32
5.29
5.63
5.63
2.89
2.25
1.81
S u l f a t e Organic Total
3.,22
Pyritic
Sulfur Distrib.
T a b l e I I I . R e s u l t s o f L e a c h i n g ISU C o a l w i t h D i f f e r e n t C o n c e n t r a t i o n s o f A l k a l i
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AL.
Alkaline Solutions tvith Dissolved Oxygen
191
PYRITE -120/+Ί40
7.8
MESH
atm.
150 °C
2
3
Figure 3. The effect of reaction time on the extraction of sulfur from pyrite
REACTION T I M E , h r .
-200 7.8
4 INITIAL
Figure 4.
6
8
SODIUM CARBONATE
10
MESH I S U COAL a t m . TOTAL P R E S S .
150° C 2.0 h r . I 12
CONCENTRATION,
I
WT. %
Sulfur content of IS U coal after leaching
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
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192
COAL
DESULFURIZATION
end o f a r u n . W a s h i n g w i t h w a t e r d i d n o t remove s o d i u m f r o m the t r e a t e d c o a l , b u t w a s h i n g w i t h d i l u t e a c i d (0.1N hydrochloric a c i d ) d i d remove i t . A n o t h e r s e r i e s o f e x p e r i m e n t s was c o n d u c t e d t o see what e f f e c t r e d u c i n g the s i z e o f t h e c o a l w o u l d have on d e s u l f u r i z a t i o n by c h e m i c a l l e a c h i n g . ISU c o a l was f i r s t p u l v e r i z e d to -35 mesh ( a b o u t 50% b e l o w 200 mesh) w i t h a M i k r o - S a m p l m i l l ( P u l v e r i z i n g Machinery D i v i s i o n , A m e r i c a n - M a r i e t t a Co.). The c o a l was t h e n wet-ground i n a ceramic j a r m i l l f o r d i f f e r e n t time p e r i o d s . The p a r t i c l e s i z e d i s t r i b u t i o n o f the c o a l a f t e r g r i n d i n g f o r 2, 4, 8, and 20 h r i s shown i n F i g u r e 6. A f t e r g r i n d i n g f o r 2 h r , 97% o f t h e c o a l was f i n e r t h a n 400 mesh (38 ym) s i z e . The p u l v e r i z e d o r g r o u n d c o a l was t h e n l e a c h e d i n t h e s t i r r e d a u t o c l a v e f o r 2 h r a t 140°C w i t h a 2.0 wt % s o l u t i o n o f s o d i u m c a r b o n a t e c o n t a i n i n g o x y g e n d i s s o l v e d u n d e r a p a r t i a l p r e s s u r e o f 2.4 atm and w i t h a t o t a l s y s t e m p r e s s u r e o f 5.8 atm. F o r e a c h l e a c h i n g r u n 25 g o f c o a l was m i x e d w i t h 500 ml o f s o l u t i o n . The r e s u l t s p r e s e n t e d i n T a b l e IV show t h a t more s u l f u r was e x t r a c t e d f r o m c o a l w h i c h had been ground i n t h e b a l l m i l l t h a n f r o m c o a l w h i c h had o n l y been p u l v e r i z e d w i t h the M i k r o - S a m p l m i l l . Thus t h e p y r i t i c s u l f u r c o n t e n t o f t h e b a l l - m i l l e d c o a l was r e d u c e d 87% w h e r e a s t h e p y r i t i c s u l f u r c o n t e n t o f t h e p u l v e r i z e d c o a l was r e d u c e d o n l y 71%. However, g r i n d i n g t h e c o a l f o r more t h a n 2 h r d i d n o t p r o duce any a d d i t i o n a l b e n e f i t . Combined P h y s i c a l and
Chemical
Cleaning
A f i n a l s e t o f e x p e r i m e n t s i n v o l v e d combined p h y s i c a l and c h e m i c a l c l e a n i n g o f s e v e r a l Iowa c o a l s . Each c o a l was c r u s h e d t o 6 mm χ 0 s i z e w i t h a d o u b l e r o l l c r u s h e r and t h e n c l e a n e d by g r a v i t y s e p a r a t i o n i n an o r g a n i c l i q u i d h a v i n g a s p e c i f i c g r a v i t y o f 1.60. The c l e a n e d f l o a t f r a c t i o n was r e c o v e r e d , d r i e d , and p u l v e r i z e d w i t h the M i k r o - S a m p l m i l l . The p u l v e r i z e d c o a l was wetg r o u n d n e x t i n t h e c e r a m i c j a r m i l l f o r 20 h r and f i n a l l y l e a c h e d i n the s t i r r e d a u t o c l a v e f o r 2.0 h r w i t h a 2.0 wt % s o d i u m c a r b o n a t e s o l u t i o n . The e f f e c t s o f d i f f e r e n t l e a c h i n g t e m p e r a t u r e s and o x y g e n p a r t i a l p r e s s u r e s were s t u d i e d . The r e s u l t s p r e s e n t e d i n T a b l e V show t h a t g r a v i t y s e p a r a t i o n removed a s u b s t a n t i a l p a r t o f the p y r i t i c s u l f u r f r o m e a c h c o a l and t h a t c h e m i c a l l e a c h i n g removed most o f the r e m a i n i n g i n o r g a n i c s u l f u r , b o t h p y r i t i c and s u l f a t e . Thus t h r o u g h t h e combined t r e a t m e n t , the i n o r g a n i c s u l f u r c o n t e n t of each of the t h r e e c o a l s was r e d u c e d 93-95%. The t r e a t e d ICO c o a l came c l o s e to m e e t i n g the f e d e r a l new s o u r c e p e r f o r m a n c e s t a n d a r d o f 0.6 l b S/10 Btu. F o r the p h y s i c a l l y c l e a n e d and f i n e l y g r o u n d c o a l , i t d i d n o t seem to make any d i f f e r e n c e what l e a c h i n g t e m p e r a t u r e i n t h e r a n g e o f 120°-150°C o r what o x y g e n p a r t i a l p r e s s u r e i n t h e r a n g e o f 2.4-5.2 atm was u s e d b e c a u s e e s s e n t i a l l y a l l o f the i n o r g a n i c s u l f u r was removed even u n d e r the m i l d e s t t r e a t m e n t c o n d i t i o n s . 6
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
ET
AL.
Alkaline Solutions with Dissolved Oxygen
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TAI
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
193
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
chemical
3-•108-8 b.mill (8hr) 11,237
11,070
b.mill
chemical
3-•108-6
(4 h r )
11,500
b.mill (2hr)
chemical
3-•108-7
11,360
11,040
H.V. (Btu/lb)
pulverized
pulverized
Grind
chemical
none
Treatment
16.2
16.6
14.7
15.8
12.0
Ash (wt %)
0.34
0.30
0.29
0.67
2.31
Pyritic
0.05
0.05
0.04
2.06
2.17
2.10
2.32
2.19
0.54 0.05
Organic
Sulfate
Sulfur Distribution (lb/10
R e s u l t s o f T r e a t i n g D i f f e r e n t G r i n d s o f ISU C o a l
3-•108-5
Run No.
Table IV.
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b
2.46
2.51
2.43
3.05
5.04
Total
Btu
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
B i g Ben B i g Ben B i g Ben B i g Ben
ICO ICO ICO ICO ICO ICO ICO
ISU ISU ISU ISU ISU
Source
25 25
—
40 40 40 25 25
—
40 40 20
—
Amt.(g)
Coal
none float/sink chemical chemical
none float/sink chemical chemical chemical chemical chemical
none float/sink chemical chemical chemical
Treatment
T a b l e V.
— 2.9 3.2
132 150
2.7 3.7 5.2 3.2 3.2
120 120 120 150 150
—
—
5.8 7.8
—
4.7 5.8 7.3 7.8 7.8
—
4.4 5.8 6.9
2.4 2.7 2.4
Total
—
2
(atm.)
—
0
Pressure
—
120 135 150
—
iemp. (°C)
11,800 12,790 10,950 11,680
12,040 12,690 11,630 11,480 11,640 11,220 11,740
10,990 12,390 11,650 11,490 10,770
η. ν . (Btu/lb)
10.6 10.0
— —
11.6 11.6 10.8 14.1 13.2
— —
Ι.37 Ο,.42 0,.09 0.16
0.,37 0.,28 0..03 0.,04
0.,25 0.,20 0.,02 0.,02 0.,02 0.,03 0.,04
0.,33 0.,23 0.,06 0.,07 0.,04
3.,96 1,,38 0,,13 0.,18 0..21 1,,66 0.,70 0,.10 0,.15 0,.09 0,.14 0.11
Sulfate
%) P y r i t i c
12.2 12.1 24.0
—
(wt
Sulfur Distrib.
R e s u l t s o f Combined P h y s i c a l and C h e m i c a l T r e a t m e n t
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,53 ,41 ,34 ,32 ,04
0..61 0,.81 0,.89 0.81
0.,62 0.,64 0.,58 0.,64 0.,60 0.,56
0. ,61
2. 2. 2. 2. 2.
2.36 1.47 1.00 1.01
2.52 1.53 0.76 0.75 0.74 0.77 0.71
6.81 4.02 2.53 2.57 2.29
Organic Total
(lb/10° B t u )
196
COAL DESULFURIZATION
T h e r e f o r e , i t s h o u l d have b e e n p o s s i b l e t o o b t a i n a s good r e s u l t s even w i t h m i l d e r treatment c o n d i t i o n s o r a s h o r t e r r e a c t i o n time.
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Conclusions D i l u t e a l k a l i n e s o l u t i o n s c o n t a i n i n g oxygen d i s s o l v e d u n d e r p r e s s u r e were v e r y e f f e c t i v e a t e l e v a t e d t e m p e r a t u r e s f o r e x t r a c t i n g t h e i n o r g a n i c s u l f u r f r o m c o a l . Of v a r i o u s a l k a l i s t e s t e d , s o d i u m c a r b o n a t e gave t h e b e s t r e s u l t s . T h i s m a t e r i a l a l s o has the advantages o f b e i n g r e a d i l y a v a i l a b l e , low i n c o s t , and r e l a t i v e l y n o n c o r r o s i v e i n aqueous s o l u t i o n t o w a r d s s t e e l and o t h e r common m a t e r i a l s o f c o n s t r u c t i o n . Although s u f f i c i e n t a l k a l i s h o u l d be u s e d t o n e u t r a l i z e a l l o f t h e a c i d w h i c h i s p r o d u c e d t h r o u g h o x i d a t i o n o f t h e c o a l s u l f u r , an e x c e s s i v e c o n c e n t r a t i o n o f a l k a l i seems t o s l o w t h e r a t e o f d e s u l f u r i z a t i o n . On t h e o t h e r h e a d , t h e r a t e o f d e s u l f u r i z a t i o n c a n be i n c r e a s e d by r e d u c i n g t h e s i z e o f t h e c o a l a n d / o r p y r i t e p a r t i c l e s . Leach i n g c o a l f i n e s w i t h d i l u t e sodium carbonate s o l u t i o n s a t tempera t u r e s up t o 150°C and w i t h o x y g e n p a r t i a l p r e s s u r e s up t o 5 atm f o r up t o 2 h r does n o t seem t o d e g r a d e h i g h v o l a t i l e b i t u m i n o u s coal. However, t h e c o a l does a d s o r b s o d i u m f r o m t h e l e a c h s o l u t i o n w h i c h c a n be removed s u b s e q u e n t l y by w a s h i n g w i t h d i l u t e acid. C h e m i c a l l e a c h i n g c a n be combined a d v a n t a g e o u s l y w i t h p h y s i c a l c l e a n i n g s i n c e t h e l a t t e r i s more a d e p t a t r e m o v i n g c o a r s e r p a r t i c l e s o f p y r i t e w h i l e t h e f o r m e r i s more a d e p t a t removing the microscopic p a r t i c l e s . Ac k n o w l e d gemen t T h i s work was s p o n s o r e d by t h e Iowa C o a l P r o j e c t and c o n d u c t e d i n t h e E n e r g y and M i n e r a l R e s o u r c e s R e s e a r c h I n s t i t u t e a t Iowa S t a t e U n i v e r s i t y .
Literature Cited
1. Nelson, H. W., Snow, R. D., Keyes, D. B., Ind. Eng. Chem. (1933) 25, 1355. 2. Agarwal, J. C., Giberti, R. Α., Irminger, P. F., Petrovic, L. J., Sareen, S. S., Min. Congr. J. (1975) 61 (3), 40. 3. Sareen, S. S., Giberti, R. Α., Irminger, P. F., Petrovic, L. J., Preprint 50c, 80th National Meeting AIChE, (Sep. 7-10, 1975), Boston. 4. Agarwal, J. C., Giberti, R. Α., Petrovic, L. J., U.S. Patent No. 3,960,513, 1976. 5. Sareen, S. S., This volume, in press. 6. Friedman, S., LaCount, R. B., Warzinski, R. P., This volume, in press. 7. Majima, Η., Peters, Ε., Trans. Metall. Soc. AIME (1966) 1409. 8. Stenhouse, J. E., Armstrong, W. M., Can. Min. Metall. Bull. (1952) 45, 49.
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.
15.
TAI
ET
AL.
Alkaline
Solutions
with
Dissolved
Oxygen
197
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9. Burkin, A. R., Edwards, Α. Μ., in "Mineral Processing," (A. Roberts, Ed.), pp. 159-169, Pergamon, Oxford, 1965. (Procedding of the Sixth International Congress held at Cannes, May 26-June 2, 1963.) 10. McKay, D. R., Halpern, J., Trans. Metall. Soc. AIME (1958) 301. 11. Book ASTM Stand., Part 26, "Gaseous Fuels; Coal and Coke; Atmospheric Analysis," Methods D2015-66, D2492-68, D3174-73, D3177-75, 1976. 12. Fritz, J. S., Yamamura, S. S., Anal. Chem. (1955) 27, 1461. 13. Anderson, J. E., Halpern, J., Samis, C. S., J. Met. (1953) 5, 554. 14. Dresher, W. H., Wadsworth, M. E., Fassell, W., Jr., J. Met. (1956) 8, 794.
In Coal Desulfurization; Wheelock, T.; ACS Symposium Series; American Chemical Society: Washington, DC, 1977.