Recovery of common salt and marine chemicals from brine
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C01D-003/00
C01F-005/00
출원번호
US-0003213
(2001-10-29)
발명자
/ 주소
Vohra, Rajinder N.
Ghosh, Pushpito Kumar
Mohandas, Vadakke Puthoor
Joshi, Himanshu Labhshanker
Deraiya, Hasina Hajibhai
Dave, Rohit Harshadray
Halder, Koushik
Yadav, Ran Bahadur
Daga, Sohan L
출원인 / 주소
Council of Scientific and Industrial Research
대리인 / 주소
Drinker Biddle & Reath LLP
인용정보
피인용 횟수 :
38인용 특허 :
2
초록▼
A new process for recovery of common salt, potassium chloride, concentrated magnesium chloride with enriched bromide, and high purity magnesia from brine in an integrated manner, said process comprises preparation of calcium chloride by reaction of hydrochloric acid generated in the process with lim
A new process for recovery of common salt, potassium chloride, concentrated magnesium chloride with enriched bromide, and high purity magnesia from brine in an integrated manner, said process comprises preparation of calcium chloride by reaction of hydrochloric acid generated in the process with limestone, desulfatation of brine with calcium chloride, production of sodium chloride of superior quality in solar pans, solar evaporation of bittern thereby producing carnallite and end bittern, processing carnallite through established processes to produce potassium chloride, recovering end bittern containing highly concentrated magnesium chloride and enriched bromide and calcination of a part of the end bittern after solidification to produce high purity magnesia and hydrochloric acid utilizable in the process.
대표청구항▼
1. A process for recovery of common salt and marine chemicals from brine in an integrated manner, said process comprising the sequential steps of:(i) treating brine with a composition comprising calcium chloride to produce a calcium sulphate precipitate;(ii) seperating the precipitated calcium sulph
1. A process for recovery of common salt and marine chemicals from brine in an integrated manner, said process comprising the sequential steps of:(i) treating brine with a composition comprising calcium chloride to produce a calcium sulphate precipitate;(ii) seperating the precipitated calcium sulphate from the brine to obtain partly desulpahted brine;(iii) treating the partly desulpahated brine obtained in step (ii) with barium chloride to obtain substantially desulphatated brine;(iv) evaporating the substantially desulphated brine thus obtained in step (iii) to a density of 29-32° Be′ to obtain crystals of common salt having a negligible amount of sulphate salts, and a bittern;(v) washing the common salt thus obtained in step (iv) with water or dilute brine to remove adhering chlorides of calcium and magnesium;(vi) evaporating the bittern obtained in step (iv) up to a density of about 35.5° Be′ to obtain crude carnallite and a concentrated end bittern comprising magnesium chloride and enriched bromide;(vii) solidifying a part of the end bittern and calcining the solidifed part to produce solid magnesium oxide and hydrochloric acid; and(viii) reacting the hydrochloric acid produced in step (vii) with a calcerous material comprising limestone to provide calcium chloride, and recycling the calcium chloride to step (i). 2. The process as claimed in claim 1, wherein the recovered marine chemicals include, potassium chloride, magnesium chloride enriched with bromide, high purity magnesia and calcium sulphate, each containing less than 0.5% chloride. 3. The process as claimed in claim 1, wherein the brine treated in step (i) has a density of 3-24° Be′. 4. The process as claimed in claim 1, wherein the composition comprising calcium chloride in step (i) is calcium chloride or soda ash distiller waste. 5. The process as claimed in claim 4, wherein the soda ash distiller waste contains 5-15% calcium chloride. 6. The process as claimed in claim 4, wherein the calcium chloride is prepared by reacting hydrochloric acid with calcerous material. 7. The process as claimed in claim 1 wherein in step (i), the calcium chloride has a concentration in the range of 100 to 600 g/L. 8. The process as claimed in claim 1 wherein in step (ii), the precipitated calcium sulphate is separated in granular form from the brine by the brine. 9. The process as claimed in claim 1 wherein in step (iii), 0.80-0.95 mole ratio of barium to residual sulphate ion in the form of BaCl 2 is used. 10. The process as claimed in claim 1 wherein in step (iv), evaporation of the bittern is carried out in solar pans. 11. The process as claimed in claim 1 wherein in step (vi), the bittern is evaporated to a density of in the range from 29 to 35.5° Be′. 12. The process as claimed in claim 1 wherein in step (vi), the crude carnallite is obtained in the form of crystals. 13. The process as claimed in claim 1 wherein in step (vi), the crude carnallite thus obtained has the composition 15.00% KCl; 28.22% MgCl 2 ; 0.46% CaSO 4 ; 0.36% CaCl 2 ; and 6.2% NaCl. 14. The process as claimed in claim 1 wherein in step (vi), the crude carnallite thus obtained is decomposed to obtain a sodium chloride and potassium chloride mixture. 15. The process as claimed in claim 14 wherein potassium chloride is recovered from the mixture. 16. The process as claimed in claim 1 wherein in step (vii), the solidified end bittern is calcined at 600 to 800° C. to obtain MgO and HCl. 17. The process as claimed in claim 1 wherein in step (i), the sulphate concentration of the brine is in the range of 5 to 18 g/L at 16° Be′. 18. The process as claimed in claim 1 wherein in step (ii), the sulphate concentration of the brine is in the range of 0.5 to 2.0 g/L. 19. The process as claimed in claim 1 wherein the brine treated in step (i) is sub-soil brine having up to 18° Be′ of sodium chloride and less than 6 g/L of sulphate at 16 0; Be′. 20. The process as claimed in claim 1 wherein the bromide concentration in the concentrated end bittern from step (vi) is up to 7.5 g/L at 35.5° Be′.
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이 특허에 인용된 특허 (2)
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