US2677667A - Process for the revivification of spent carbonaceous material - Google Patents

Process for the revivification of spent carbonaceous material Download PDF

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US2677667A
US2677667A US216348A US21634851A US2677667A US 2677667 A US2677667 A US 2677667A US 216348 A US216348 A US 216348A US 21634851 A US21634851 A US 21634851A US 2677667 A US2677667 A US 2677667A
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Howarth Peter Francis Wildman
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Colonial Sugar Refining Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/30Active carbon
    • C01B32/354After-treatment
    • C01B32/36Reactivation or regeneration
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S502/00Catalyst, solid sorbent, or support therefor: product or process of making
    • Y10S502/515Specific contaminant removal
    • Y10S502/517Sulfur or sulfur compound removal

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  • This invention relates to an improved process for the revivification of adsorbent material of a carbonaceous nature, such as bone char, used to remove colouring matter from liquors in various refining processes such as, for example, the refining of sugar.
  • superheated steam On the industrial scale one of the most convenient of such heat transfer gases is superheated steam. It is conveniently available and has a suitably high specific heat so that it can be made to transfer heat efficiently to the surface of each individual grain of char. However, apart from this highly desirable physical property superheated steam has a specific chemical reaction with carbonaceous matter which may, or may not, be of assistance in reactivating bone char.
  • the object of the present invention is to provide a process of revivifying bone char and similar spent carbonaceous adsorptive materials with superheated steam which process is substantially free of undesirable side reactions.
  • a process for reviviiying spent carbonaceous adsorptive materials comprises treating the spent material with superheated steam and thereafter treating the material with a gas containing carbon dioxide and thoroughly mixing the treated material before reusing.
  • Saturated steam at p. s. i. g. pressure is passed into a trap I and then through a reducing valve 2 into a superheater 3 consisting of an Inconel tube 4 in an electric furnace.
  • the superheated steam then passes along line 5 to a revivifying vessel 6 containing the material to be treated and from the revivifying vessel to a condenser 'l'.
  • the revivifying vessel 5 consists of a fixed outer shell fitted with an outlet pipe at the bottom and a removable lid at the top.
  • a removable inner vessel of lighter construction holds the material to be treated.
  • the top of this inner vessel is open and the bottom perforated to retain the ma-' terial while allowing the steam to pass through.
  • the small annular space between the walls of this inner vessel and the outer shell are plugged so that steam cannot by-pass the bed.
  • a by-pass line 8 to divert steam not properly heated is provided.
  • Aline 5 to feed cool steam or other gas or vapour to the revivifying vessel is also provided.
  • the superheater 3, the superheated steam line 5 and the reviviiying vessel are closely lagged and provided with thermocouples l0, H and 12 respectively.
  • the rate of steam flow is measured by the rate of condensation in condenser 1.
  • Fig. 2 of the accompanying drawing gives, during a typical run, a time record of the temperature at three different points in the vessel--near the bottom, near the centre and near the top-the traverse being along the axis of the vessel.
  • the treated material may be cooled by passing gases containing CO2 into the revivifying vessel instead of the cool saturated steam.
  • the rate of steam flow is so adjusted that the central temperature of the material being treated is brought to a temperature of 900 F. as quickly as possible and maintained at that temperature for the duration of the treatment.
  • While the preferred operating temperature of the superheated steam revivification process is approximately 900 F. the process may be carried out at any temperature within the range 800"-11'00 F.
  • the time of treatment of the material with the superheated steam varies with the temperature at which the treatment is effected, the higher the temperature the shorter the duration of treatment.
  • the duration of treatment is also dependent on the nature of material i. e. whether it is only partially spent or whether it is completely spent. Tests are made at appropriate intervals to determine the relative colour adsorptive capacity. When this reaches a predetermined level the steam treatment is discontinued.
  • Any gas containing a suitable proportion of carbon dioxide may be used to treat or cool the supersaturated steam treated char. Flue gases, containing 8-20% carbon dioxide, may be conveniently used. The proportion of carbon dioxide, however, is not critical and gases containing much more or much less carbon dioxide may be used satisfactorily.
  • Material treated with flue gases in accordance with the present invention absorbs carbon dioxid '1 very rapidly, so rapidly indeed that the eifective Table I pH near the gas inlet is brought down to about pH'7 before any CO reaches the top of the tower.
  • suitable mixing gives a material of satisfactory characteristics.
  • EXAMPLE I 4 lbs. of exhausted char from a sugar refinery were packed in a reactor vessel of 4 inches internal diameter fitted with a central thermocouple well. Steam superheated to 1100 F. was admitted at such a rate that the velocity through the bed was 2 feet per second. The temperature rose rapidly to 850 C. and was maintained between that temperature and 900 C. for 30 minutes by throttling back the rate of steam flow to 1 foot per second. The char was then cooled in a stream of dry steam, treated with a current of pure CO2 at a flow rate of 0.5 foot per second for 3 minutes, and finally mixed by transference to another vessel. The resultant revivified char which had a pH of 10.9 before treatment with CO2 had now a pH of 7.8, contained 3.75% CaCOs, and gave a very satisfactory performance in the miniature cistern test.
  • EXANLPLE II 20 lbs. of exhausted char were revivified in four separate batches according to the technique given in Example I, but at a higher temperature (namely a maximum of 1,000 K). The four batches were thoroughly mixed and 4 lbs. were put away for testing. The remaining 16 lbs. were exhausted by treatment with raw liquor until a distinct caramel colour ran through the char. The char was then Washed, dried and regenerated according to the technique above. The different batches were mixed and 4 lbs. again placed on one side and the rest exhausted. In this way samples were obtained of char which had passed through up to five cycles of exhaustion and regeneration.
  • the effective char pH was measured by extraction with 1% calcium acetate solution using Waynes method; the char was analysed for carbon, silica, calcium sulphate, ferric oxide, calcium sulphide, calcium carbonate, calcium phosphate and for organic matter; the friability of the char was determined and so was the intensity of colour extracted by boiling for one minute with 2.5% caustic soda solution.
  • the decolourizin efficiency was determined by a miniature cistern test.
  • the adsorptive power of the char for caramel colours was recorded in terms of the volume of fine liquor delivered from the char bed when a certain definite amount of colour had been developed.
  • Such a test is of the form of the usual break-point tests used in examining the adsorptive properties of gas absorbent carbons.
  • the relative friability of the char was determined by means of a test in which the char was treated in a mill for a standard time and the fines produced were weighed. The higher the weight of fines the more friable the char. Relative figures were obtained by expressing the friability of the initial untreated char for any given set of determinations, as one hundred.
  • the first sample of spent char to be examined was treated at 900 F. for half anhour.
  • the char obtained was extremely alkaline not only in the sense of having a high pH but also in requiring a large amount of acid to bring it to neutrality.
  • the char obviously contained much free calcium oxide. It had evidently been treated at too high a temperature.
  • spent adsorptive carbonaceous material refers to carbonaceous material such as activated charcoal, bone char or the like, the adsorptive capacity of which has been exhausted by use in a chemical refining process, such as the clarification of raw sugar liquors.
  • a process for the revivification of spent carbonaceous adsorptive material which comprises passing superheated steam at a temperature within the range of 800 F.-1100 F. through the spent material for 3-4 hours, cooling the material, passing gases containing carbon dioxide up through the material until the pH of the material is approximately 7 and the CaCO3 content of the material is substantially equivalent to that of the original carbonaceous adsorptive material and thoroughly mixing the treated material.
  • a process for the revivification of spent carbonaceous adsorptive material which comprises passing superheated steam at a temperature within the range of 800 F.-l100 F. through the spent material until a sample of the material gives a substantially negative colour reaction on boiling for one minute with 2.5% caustic soda solution, cooling the material, passing gases containing carbon dioxide through the material until carbon dioxide can be detected in the gases emerging from the material, and thoroughly mixing the sotreated material, which has a CaCOz content substantially equivalent to that of the original carbonaceous adsorptive material.
  • a process for the revivification of spent bone char which comprises passing superheated steam through the bone char so that the temperature thereof is maintained at approximately 900 F. and until a sample gives a substantially negative dilute caustic soda colour, cooling the bone char, passing flue gases containing 820% of carbon dioxide through the bone char until carbon dioxide can be detected emerging from the bone char thereby restoring the CaCO; content of the bone char to substantially the same level as that of the original bone char and thoroughly mixing the so-treated bone char.

Description

May 4, 1954 F. W. HOWARTH PROCESS FOR THE REVIVIFICATION OF SPENT CARBONACEOUS MATERIAL Filed March 19, 1951 uuu 4 coolms 3 BURNING COL UMN TIME IN HOURS.
TEMP. IN 0 F.
5 2 PETER FRANCIS w/wm/v ww/mry INVENTOR Patented May 4, 1954 UNITED STATES TENT OFFICE PROCESS FOR THE REVIVIFIGATION F SPENT CARBONACEOUS MATERIAL Application March 19, 1951, Serial No. 216,348
3 Claims.
This invention relates to an improved process for the revivification of adsorbent material of a carbonaceous nature, such as bone char, used to remove colouring matter from liquors in various refining processes such as, for example, the refining of sugar.
in the past revivification of bone char has been carried out by burning in Scotch kilns. This produces an irregularly treated material, part of the char being overburnt and part underburnt. Presumably this is due to the quite severe temperature differences throughout the lrilns. Such temperature differences are probably due to the poor thermal conductivity of the char, which has been given as 0.09 B. t. u. feet hour Ti- This low thermal conductivity is of the same order as that of asbestos. The irregular performance of the Scotch kilns may also be due to the low thermal diliusivity of bone char, being only 0.0080 feet hours In a material of such low thermal diffusivity it takes a long time to smooth out any local temperature irregularities.
Numerous attempts have been made to overcome the disadvantages of the Scotch kiln treatment by supplying heat internally to spent char by treating the char with a heated gas or vapour. Exemplary or" these is the Herreshofi furnace which uses direct heating by combustion gases from an oil burner.
On the industrial scale one of the most convenient of such heat transfer gases is superheated steam. It is conveniently available and has a suitably high specific heat so that it can be made to transfer heat efficiently to the surface of each individual grain of char. However, apart from this highly desirable physical property superheated steam has a specific chemical reaction with carbonaceous matter which may, or may not, be of assistance in reactivating bone char.
The use of superheated steam to reactivate bone char has been made the subject of a number of patents. However, while it appears that the steam reactivation process ofiers, at least on paper, some considerable advantages over the normal process, it is not at all clear from the literature whether such advantages may be realised without complications due to undesirable side reactions.
The object of the present invention, therefore, is to provide a process of revivifying bone char and similar spent carbonaceous adsorptive materials with superheated steam which process is substantially free of undesirable side reactions.
It is also an object or" the present invention to provide a process of revivifying bone char and similar materials without substantially impairing the desirable characteristics of the material.
(Cl. 252-- i20) According to the present invention a process for reviviiying spent carbonaceous adsorptive materials comprises treating the spent material with superheated steam and thereafter treating the material with a gas containing carbon dioxide and thoroughly mixing the treated material before reusing.
The method of revivification according to the process of the present invention may be conveniently carried out in apparatus such as that shown diagrammatically in Fig. 1 or" the accompanying drawing. However it should be understood that the invention is not limited to the use of the particular apparatus disclosed herein. Any other suitable form of apparatus may be used if desired.
Saturated steam at p. s. i. g. pressure is passed into a trap I and then through a reducing valve 2 into a superheater 3 consisting of an Inconel tube 4 in an electric furnace. The superheated steam then passes along line 5 to a revivifying vessel 6 containing the material to be treated and from the revivifying vessel to a condenser 'l'.
The revivifying vessel 5 consists of a fixed outer shell fitted with an outlet pipe at the bottom and a removable lid at the top. A removable inner vessel of lighter construction holds the material to be treated. The top of this inner vessel is open and the bottom perforated to retain the ma-' terial while allowing the steam to pass through. The small annular space between the walls of this inner vessel and the outer shell are plugged so that steam cannot by-pass the bed.
A by-pass line 8 to divert steam not properly heated is provided. Aline 5 to feed cool steam or other gas or vapour to the revivifying vessel is also provided. The superheater 3, the superheated steam line 5 and the reviviiying vessel are closely lagged and provided with thermocouples l0, H and 12 respectively. The rate of steam flow is measured by the rate of condensation in condenser 1.
The revivifying vessel 6 is heated only by the superheated steam and Fig. 2 of the accompanying drawing gives, during a typical run, a time record of the temperature at three different points in the vessel--near the bottom, near the centre and near the top-the traverse being along the axis of the vessel.
In carrying out the process of the present invention superheated steam at an initial temperature of 800 F. is passed into the reviviiying vessel packed with the spent material. The temperature is then raised as rapidly as possible to 1100 F. and maintained there for the duration of the treatment. Under the influence of this heated 3 steam the material, in at least the major part of the reactivating vessel, is maintained at 900 F. for the greater part of the cycle. It will be evident from a consideration of Fig. 2 that there is some tendency for the low portion of the vessel to be cooler with the result that the material in this section tends to be underburnt. After the treatment with superheated steam is complete the material is cooled by admitting cool saturated steam to the vessel. The freshly revivified material is then packed in an open tower and gases containing CO2 passed up through the material until CO2 can be detected in the gases emerging from the top of the tower. The material so treated is then thoroughly mixed before reusing.
Alternatively the treated material may be cooled by passing gases containing CO2 into the revivifying vessel instead of the cool saturated steam.
In the cycle illustrated in Fig. 2 the reaction vessel was maintained at a temperature of approximately 900 F. for about four hours. The maintenance of these particular timetempera ture curves is dependent on the rate of steam flow. The curves as shown in Fig. 2 are obtained when the steam flow has a linear velocity of l foot/sec. at a pressure of 15 p. s. i. g.
In carrying out the process of the present invention the rate of steam flow is so adjusted that the central temperature of the material being treated is brought to a temperature of 900 F. as quickly as possible and maintained at that temperature for the duration of the treatment.
While the preferred operating temperature of the superheated steam revivification process is approximately 900 F. the process may be carried out at any temperature within the range 800"-11'00 F.
The time of treatment of the material with the superheated steam varies with the temperature at which the treatment is effected, the higher the temperature the shorter the duration of treatment. The duration of treatment is also dependent on the nature of material i. e. whether it is only partially spent or whether it is completely spent. Tests are made at appropriate intervals to determine the relative colour adsorptive capacity. When this reaches a predetermined level the steam treatment is discontinued.
Any gas containing a suitable proportion of carbon dioxide may be used to treat or cool the supersaturated steam treated char. Flue gases, containing 8-20% carbon dioxide, may be conveniently used. The proportion of carbon dioxide, however, is not critical and gases containing much more or much less carbon dioxide may be used satisfactorily.
Material treated with flue gases in accordance with the present invention absorbs carbon dioxid '1 very rapidly, so rapidly indeed that the eifective Table I pH near the gas inlet is brought down to about pH'7 before any CO reaches the top of the tower. However, despite the unevenness of the pH throughout the bed of material, suitable mixing gives a material of satisfactory characteristics.
The following is an example of the revivification of bone char in accordance with the inven tion.
EXAMPLE I 4 lbs. of exhausted char from a sugar refinery were packed in a reactor vessel of 4 inches internal diameter fitted with a central thermocouple well. Steam superheated to 1100 F. was admitted at such a rate that the velocity through the bed was 2 feet per second. The temperature rose rapidly to 850 C. and was maintained between that temperature and 900 C. for 30 minutes by throttling back the rate of steam flow to 1 foot per second. The char was then cooled in a stream of dry steam, treated with a current of pure CO2 at a flow rate of 0.5 foot per second for 3 minutes, and finally mixed by transference to another vessel. The resultant revivified char which had a pH of 10.9 before treatment with CO2 had now a pH of 7.8, contained 3.75% CaCOs, and gave a very satisfactory performance in the miniature cistern test.
In order to determine whether or not the process of revivifying bone char in accordance with the present invention resulted in a progressive deterioration of the known characteristics, char, which had been reactivated by treatment with superheated steam followed by treatment with flue gas which restored the effective pH to the normal value for fresh char, was subjected to a series of cyclic treatments of exhaustion with raw sugar liquors followed by regeneration.
EXANLPLE II 20 lbs. of exhausted char were revivified in four separate batches according to the technique given in Example I, but at a higher temperature (namely a maximum of 1,000 K). The four batches were thoroughly mixed and 4 lbs. were put away for testing. The remaining 16 lbs. were exhausted by treatment with raw liquor until a distinct caramel colour ran through the char. The char was then Washed, dried and regenerated according to the technique above. The different batches were mixed and 4 lbs. again placed on one side and the rest exhausted. In this way samples were obtained of char which had passed through up to five cycles of exhaustion and regeneration.
Samples of the revivified char were taken after each revivification, freed from iron scale and ground to dust and then analysed chemically. The properties of the different samples are set out below in Table I.
CHANGES IN THE PROPERTIES OF CHAR ON REPEAIED STEAM REVIVIFICATION FOL- LOWED BY NEUTRALIZATION VVIIH CARBON DIOXIDE Relative Relative pH Chemical Adsorptive Adsorptive Cycle No Capacity Capacity Relative for Colors for Ash Friability Fin 1 1n Raw in Raw Char Li a Carbon OaCOa Ca s. CaSO Liquor Liquor quot It will be seen that while there is slight decrease in the absorptive capacities on the first steam regenerations, there is a pronounced increase in adsorptive capacities in the later cycles. As far as the relative friabilities of the chars are concerned no significant change appears to occur. On the side of chemical analysis no significant changes occur other than the desirable decrease in the Gas content, and a relatively smaller but nevertheless significant decrease in the carbon content of the char. This decrease in the carbon content may even be associated with the increase in the absorptive capacities. The original char used in these tests apparently contained a little too much carbon. There is no deleterious efiect on the pH of the char or the liquor running therefrom.
The repeated cycles of reactivation by the treatment described above, alternating with exhaustion by raw sugar liquor results in a progressive increase in activity which appears to be associated with a progressive decrease in the carbon content. This particular action of steam on char is reminiscent of its action in the production of gas-absorbed activated carbon. The superheated steam appears to selectively oxidise those carbonaceous constituents of low adsorptive capacity leaving those of higher adsorptive capacity.
To illustrate the efiectiveness of the treatment with gases containing carbon dioxide bone char was subjected to treatment with supersaturated steam only, and at various temperatures. The chars thus obtained were then analysed in accordance with the following analytical methods:
The effective char pH was measured by extraction with 1% calcium acetate solution using Waynes method; the char was analysed for carbon, silica, calcium sulphate, ferric oxide, calcium sulphide, calcium carbonate, calcium phosphate and for organic matter; the friability of the char was determined and so was the intensity of colour extracted by boiling for one minute with 2.5% caustic soda solution. In addition the decolourizin efficiency Was determined by a miniature cistern test. In this test the adsorptive power of the char for caramel colours was recorded in terms of the volume of fine liquor delivered from the char bed when a certain definite amount of colour had been developed. Such a test is of the form of the usual break-point tests used in examining the adsorptive properties of gas absorbent carbons. A similar break-point test was applied to the ash content of the liquor running off the char. A raw liquor, of standardized colour and ash content was passed at a standard rate over a bed of the treated char. The volume of liquor delivered was noted both when the colour and the ash content of the ei'lluent had reached predetermined values.
The relative friability of the char was determined by means of a test in which the char was treated in a mill for a standard time and the fines produced were weighed. The higher the weight of fines the more friable the char. Relative figures were obtained by expressing the friability of the initial untreated char for any given set of determinations, as one hundred.
The properties of the chars so treated and analysed are set out below:
The first sample of spent char to be examined was treated at 900 F. for half anhour. The char obtained was extremely alkaline not only in the sense of having a high pH but also in requiring a large amount of acid to bring it to neutrality.
The char obviously contained much free calcium oxide. It had evidently been treated at too high a temperature.
The char treatment temperature was then dropped to 800 F., time of treatment again being half an hour. The result of this treatment was still highly alkaline and in addition gave a distinct colour reaction on the caustic soda treatment. It thus appears that while considerable CaCOa had been burnt to CaO there still remained incompletely decomposed organic matter in the char. In other words features symptomatic of both underburning and overburning were present.
In further runs the temperature of treatment was reduced to 680 F. In this instance the effective pH of the resultant treated char was normal, but, as expected, the caustic soda color was abnormally high. Prolonged treatment at this same temperature tended to raise the effective char pH without appreciably reducing the colour of the caustic soda extract.
When such alkaline char is used for the treatmerit of raw sugar liquors the CaO is dissolved in the liquor, some sugars are destroyed and changed into saccharinic acids with the result that the ash content of the liquor is increased and the char bed permanently loses some of its CaCOa. Successive treatment of char by exhaustion in the miniature cistern and revivification in steam to a satisfactory NaOI-I color test showed an alarming cumulative drop in the CaCOs content of the char as indicated in Table II.
Table II CUMULATIVE Loss or (gig IN STEAM REVIVIFIED Percent Char 02.0 0:
Original 4. 6 After one cycle 2. 7 After two cycles 1. 5
The formation of free lime in steam revivified char, leading to high alkalinity, is of course due to the dissociative reaction CaCOse- -CaO +002 CaS+H2O=CaO+H2S and there is similar evidence that this loss would be cumulative over repeated regenerations. Some figures showing this progressive loss are given in Table III.
Table IH CUMULATIVE Loss OF CaS IN STEAM REVIVIFIED CHAR Percent Char 083 Original After one cycle After three cycles. After five cycles In contradistinction to CaCOa, the substance Gas is a most undesirable constituent of char from the point of view of the sugar refiner and this rapidly cumulative loss by steam revivification is a point in favour of this method.
With regard to its adsorptive properties steam revivified char proved at least comparable to ordinary char.
It will be evident from the above that the treatment of bone char with superheated steam results in (1) an undesirable reduction in the CaCOa content of the char, and (2) a desirable reduction in the Gas content of the char. The suecessive treatment of the steam treated char with gases containing carbon dioxide efiectively restores the CaCOa content and adjusts the effective pH to a satisfactory level.
The term spent adsorptive carbonaceous material as used in the description and claims refers to carbonaceous material such as activated charcoal, bone char or the like, the adsorptive capacity of which has been exhausted by use in a chemical refining process, such as the clarification of raw sugar liquors.
I claim:
1. A process for the revivification of spent carbonaceous adsorptive material which comprises passing superheated steam at a temperature within the range of 800 F.-1100 F. through the spent material for 3-4 hours, cooling the material, passing gases containing carbon dioxide up through the material until the pH of the material is approximately 7 and the CaCO3 content of the material is substantially equivalent to that of the original carbonaceous adsorptive material and thoroughly mixing the treated material.
2. A process for the revivification of spent carbonaceous adsorptive material which comprises passing superheated steam at a temperature within the range of 800 F.-l100 F. through the spent material until a sample of the material gives a substantially negative colour reaction on boiling for one minute with 2.5% caustic soda solution, cooling the material, passing gases containing carbon dioxide through the material until carbon dioxide can be detected in the gases emerging from the material, and thoroughly mixing the sotreated material, which has a CaCOz content substantially equivalent to that of the original carbonaceous adsorptive material.
3. A process for the revivification of spent bone char which comprises passing superheated steam through the bone char so that the temperature thereof is maintained at approximately 900 F. and until a sample gives a substantially negative dilute caustic soda colour, cooling the bone char, passing flue gases containing 820% of carbon dioxide through the bone char until carbon dioxide can be detected emerging from the bone char thereby restoring the CaCO; content of the bone char to substantially the same level as that of the original bone char and thoroughly mixing the so-treated bone char.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 309,222 Gray Dec, 1 1884 1,616,073 Arentz Feb. 1, 1927 1,619,327 Backhams Mar. 1, 1927 l,993,345 Jones Mar. 5, 1935 2,587,425 Adams Feb. 26, 1952 FOREIGN PATENTS Number Country Date 240,126 Great Britain Feb. 11, 1926

Claims (1)

1. A PROCESS FOR THE REVIVIFICATION OF SPENT CARBONACEOUS ADSORPTIVE MATERIAL WHICH COMPRISES PASSING SUPERHEATED STEAM AT A TEMPERATURE WITHIN THE RANGE OF 800* F.-1100* F. THROUGH THE SPENT MATERIAL FOR 3-4 HOURS, COOLING THE MATERIAL, PASSING GASESCONTAINING CARBON DIOXIDE UP THROUGH THE MATERIAL UNTIL THE PH OF THE MATERIAL IS APPROXIMATELY 7 AND THE CACO3 CONTENT OF THE MATERIAL IS SUBSTANTIALLY EQUIVALENT TO THAT OF THE ORIGINAL CARBONACEOUS ADSORPTIVE MATERIAL AND THOROUGHLY MIXING THE TREATED MATERIAL.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4252571A (en) * 1979-11-21 1981-02-24 Calgon Corporation Bone char and activated carbon mixtures for sugar liquor purification

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US309222A (en) * 1884-12-16 Method of cleansing or revivifying bone black
GB240126A (en) * 1924-09-17 1926-02-11 Arthur August Backhaus A process for revivifying activated charcoal used in the purification of fermentation carbon dioxide
US1616073A (en) * 1924-10-25 1927-02-01 Us Ind Alcohol Co Revivifying process for carbons
US1619327A (en) * 1924-09-27 1927-03-01 Us Ind Alcohol Co Process of revivifying carbon
US1993345A (en) * 1933-07-14 1935-03-05 Adico Dev Corp Process of revivifying adsorbents
US2587425A (en) * 1949-04-30 1952-02-26 Standard Oil Dev Co Reforming naphtha with activated carbon catalyst

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US309222A (en) * 1884-12-16 Method of cleansing or revivifying bone black
GB240126A (en) * 1924-09-17 1926-02-11 Arthur August Backhaus A process for revivifying activated charcoal used in the purification of fermentation carbon dioxide
US1619327A (en) * 1924-09-27 1927-03-01 Us Ind Alcohol Co Process of revivifying carbon
US1616073A (en) * 1924-10-25 1927-02-01 Us Ind Alcohol Co Revivifying process for carbons
US1993345A (en) * 1933-07-14 1935-03-05 Adico Dev Corp Process of revivifying adsorbents
US2587425A (en) * 1949-04-30 1952-02-26 Standard Oil Dev Co Reforming naphtha with activated carbon catalyst

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4252571A (en) * 1979-11-21 1981-02-24 Calgon Corporation Bone char and activated carbon mixtures for sugar liquor purification

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