GB813072A - Sulphite pulping process - Google Patents

Sulphite pulping process

Info

Publication number
GB813072A
GB813072A GB39672/56A GB3967256A GB813072A GB 813072 A GB813072 A GB 813072A GB 39672/56 A GB39672/56 A GB 39672/56A GB 3967256 A GB3967256 A GB 3967256A GB 813072 A GB813072 A GB 813072A
Authority
GB
United Kingdom
Prior art keywords
stage
liquor
magnesium
tank
digester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB39672/56A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SMITH PAPER MILLS Ltd HOWARD
Original Assignee
SMITH PAPER MILLS Ltd HOWARD
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SMITH PAPER MILLS Ltd HOWARD filed Critical SMITH PAPER MILLS Ltd HOWARD
Publication of GB813072A publication Critical patent/GB813072A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/04Pulping cellulose-containing materials with acids, acid salts or acid anhydrides
    • D21C3/06Pulping cellulose-containing materials with acids, acid salts or acid anhydrides sulfur dioxide; sulfurous acid; bisulfites sulfites
    • D21C3/10Pulping cellulose-containing materials with acids, acid salts or acid anhydrides sulfur dioxide; sulfurous acid; bisulfites sulfites magnesium bisulfite
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/10Greenhouse gas [GHG] capture, material saving, heat recovery or other energy efficient measures, e.g. motor control, characterised by manufacturing processes, e.g. for rolling metal or metal working

Landscapes

  • Paper (AREA)

Abstract

<PICT:0813072/IV (a)/1> Cellulosic raw material is pulped with a hot magnesium bisulphite solution at a digestion temperature of at least 160 DEG C., the solution being essentially free of "excess" sulphurous acid and being maintained at a pH of 3.0-4.0 during most of the digestion period. By "excess" sulphurous acid is meant the excess of "free" over "combined" acid. Preferred conditions comprise a temperature of 160-190 DEG C., an initial solution pH of 3.5-5.0, and a pressure such that the sulphurous acid liberated is retained in the digester to accelerate pulping, particularly a pressure slightly greater than the vapour pressure of water at the digester temperature. The pulp may be separated from the residual digesting liquor and the liquor concentrated and burned to recover heat, magnesium oxide and sulphur dioxide. The magnesium oxide may be slurried with water and the resulting magnesia treated with the sulphur-dioxide-containing combustion gases to form a magnesium bisulphite solution fit for further use without being "fortified" with additional sulphur dioxide. The entire process including the recovery of reagent may be effected in the apparatus shown. In stage (1) chips in digester 10 are steamed to displace air. (2) Magnesium bisulphite solution from stage (6), pre-heated in accumulator tank 11, is pumped to 10 until 5-6 atmospheres pressure is attained. (3) Surplus liquor is drained from 10 until the desired liquor to wood ratio is reached and returned to 11. (4) Digester 10 is raised to required temperature and held there for the required time, maintaining a pressure rather above the water vapour pressure at the working temperature. (5) Digester pressure is reduced, steam passing if required to 11, which also absorbs sulphur dioxide in the relief gases from stages (4) and (5). In stage (6) digester contents are discharged to blow tank 12, freeing digester for stage (1), and steam released is condensed in condenser 8, which discharges to hot water accumulator 45. (7) Pulp in 12 is suspended in a portion of the residual liquor recycled from rotary washer 13 to which the thus diluted stock is delivered, where it is washed with dilute liquor from rotary washer 14, pulp passing to stage (8) and remaining residual liquor to stage (9). (8) Partially washed pulp from 13 passes to 14 and is washed with hot water from 45, and washed pulp is then screened, cleaned and/or bleached and converted to sheeted pulp or to paper. (9) Hot residual liquor from (7) is sprayed into evaporator 18 where it meets hot flue gases from magnesia separating cyclones 25 of a chemical recovery furnace unit 24, stage (12), thus cooling the gas and partially evaporating the liquor. In stage (10) the liquor is brought to pH 6-7 at mixer 19 with make-up or recovered magnesium oxide and passes from tank 20 to multiple-effect evaporator 21, where it is concentrated to 45-70 per cent solids. (11) Evaporated liquor is then fired in recovery furnace 24, thus recovering heat and yielding steam, magnesium oxide and sulphur dioxide. (12) Magnesium oxide passes through heat exchangers and to cyclones 25 and in stage (13) is slurried in water at 26, collected in tank 30 and filtered at wash filter 32 to remove soluble alkali salts and calcium sulphate, the filter cake being reslurried and slaked at tank 33. (16) The gas from 25 passes through evaporator 18, where it is saturated with water as in stage (9), and passes to primary absorption towers 28, 29, where it meets a slurry containing washed recovered magnesium hydroxide obtained from slaking tank 33. The sulphur dioxide from the gas is absorbed, so forming magnesium bisulphite and a little magnesium monosulphite. (15) The resultant magnesium bisulphite liquor is filtered at 40 to remove silicates &c. and run from storage tank 44 to the accumulator 11 for return to cycle at stage (2). (16) Effluent gas from stage (14), which has been stripped of magnesium oxide and sulphur dioxide, is cooled by a counter-current of water in condensing tower 42, the hot water produced being available at tank 43 for use in bleaching the pulp and for other purposes. Losses of magnesium oxide from the system are made up by supplying magnesium sulphate to liquor at stage (11) or by adding oxide to hydroxide to slurry passing to stage (14), while sulphur dioxide can be made up at stage (14), or can be added to filtered liquor in accumulator 11. The process may be adapted to continuous digestion and may be applied to mixed stands of wood, including "refractory" species such as pine and Douglas fir. U.S.A. Specifications 2,285,876 and 2,385,955 are referred to.
GB39672/56A 1956-01-13 1956-12-31 Sulphite pulping process Expired GB813072A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US55891856A 1956-01-13 1956-01-13
US625164A US3046182A (en) 1956-01-13 1956-11-29 Sulphite pulping process

Publications (1)

Publication Number Publication Date
GB813072A true GB813072A (en) 1959-05-06

Family

ID=27071896

Family Applications (1)

Application Number Title Priority Date Filing Date
GB39672/56A Expired GB813072A (en) 1956-01-13 1956-12-31 Sulphite pulping process

Country Status (3)

Country Link
US (1) US3046182A (en)
DE (1) DE1249666C2 (en)
GB (1) GB813072A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1300822B (en) * 1960-04-27 1975-01-09 Process for the production of pulp

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1198666B (en) * 1961-10-20 1965-08-12 Metallgesellschaft Ag Process for the production of pulp
US3210237A (en) * 1963-04-15 1965-10-05 Boise Cascade Corp Bisulphite pulping of pine wood
US3844879A (en) * 1972-10-30 1974-10-29 Babcock & Wilcox Co System for removing sodium chloride contaminants from a magnesium base pulping process
DE2445523A1 (en) * 1974-09-24 1976-04-01 Waldhof Aschaffenburg Papier METHOD FOR MANUFACTURING PULP
US8317975B2 (en) 2004-04-20 2012-11-27 The Research Foundation Of The State University Of New York Product and processes from an integrated forest biorefinery
WO2019090414A1 (en) 2017-11-09 2019-05-16 Iogen Corporation Low temperature pretreatment with sulfur dioxide
WO2019090413A1 (en) 2017-11-09 2019-05-16 Iogen Corporation Low temperature sulfur dioxide pretreatment
EP3775243A4 (en) 2018-04-06 2022-02-09 Iogen Corporation Pretreatment with lignosulfonic acid

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US260749A (en) * 1882-07-11 Making and for textile and other purposes
US1848661A (en) * 1932-03-08 of berlin
US1052851A (en) * 1912-03-13 1913-02-11 Philadelphia Storage Battery Process of treating wood separators for storage batteries.
US1722993A (en) * 1921-11-03 1929-08-06 Bradley Linn Production of pulp
US1792510A (en) * 1925-07-01 1931-02-17 Brown Co Kraft-simulating pulp and process of producing same
US1870944A (en) * 1926-09-02 1932-08-09 Bradley Mckeefe Corp Production of pulp, etc.
US1880042A (en) * 1929-10-26 1932-09-27 Brown Co Acid process of fiber liberation
US1848780A (en) * 1930-04-16 1932-03-08 of stockholm
GB400974A (en) * 1932-03-04 1933-11-06 Henry Dreyfus Improvements in or relating to the production of cellulosic materials or cellulose
US2285876A (en) * 1938-01-26 1942-06-09 George H Tomlinson Waste sulphite liquor recovery
US2385955A (en) * 1941-04-08 1945-10-02 George H Tomlinson Manufacture of sulphite pulp
BE496841A (en) * 1949-07-12
US2716589A (en) * 1951-04-20 1955-08-30 Kaiser Aluminium Chem Corp Process of re-forming magnesium bisulfite solution

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1300822B (en) * 1960-04-27 1975-01-09 Process for the production of pulp
DE1300822C2 (en) * 1960-04-27 1975-01-09 Howard Smith Paper Mills Ltd., Montreal, Quebec (Kanada) PROCESS FOR THE RECOVERY OF PULP

Also Published As

Publication number Publication date
DE1249666B (en) 1974-05-22
DE1249666C2 (en) 1974-05-22
US3046182A (en) 1962-07-24

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