EP1204767B1 - Membranfiltrationsverfahren fur zuckerrüben - Google Patents

Membranfiltrationsverfahren fur zuckerrüben Download PDF

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Publication number
EP1204767B1
EP1204767B1 EP00957444A EP00957444A EP1204767B1 EP 1204767 B1 EP1204767 B1 EP 1204767B1 EP 00957444 A EP00957444 A EP 00957444A EP 00957444 A EP00957444 A EP 00957444A EP 1204767 B1 EP1204767 B1 EP 1204767B1
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EP
European Patent Office
Prior art keywords
ultrafiltration
juice
permeate
retentate
membrane
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EP00957444A
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English (en)
French (fr)
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EP1204767A2 (de
Inventor
Richard C. Reisig
Jatal D. Mannapperuma
Michael Donovan
Robert P. Jansen
Marc Hlavacek
Gordon Walker
John C. Williams
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Tate & Lyle Sugar Holdings Inc
Tate and Lyle Industries Ltd
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Tate and Lyle Industries Ltd
Tate & Lyle Sugar Holdings Inc
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Priority claimed from US09/376,026 external-priority patent/US6387186B1/en
Priority claimed from US09/618,416 external-priority patent/US6406547B1/en
Priority claimed from US09/618,831 external-priority patent/US6440222B1/en
Application filed by Tate and Lyle Industries Ltd, Tate & Lyle Sugar Holdings Inc filed Critical Tate and Lyle Industries Ltd
Priority to EP07003541A priority Critical patent/EP1788099A2/de
Priority to EP07003542A priority patent/EP1788100A2/de
Publication of EP1204767A2 publication Critical patent/EP1204767A2/de
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Publication of EP1204767B1 publication Critical patent/EP1204767B1/de
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    • C—CHEMISTRY; METALLURGY
    • C13—SUGAR INDUSTRY
    • C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B10/00—Production of sugar juices
    • C—CHEMISTRY; METALLURGY
    • C13—SUGAR INDUSTRY
    • C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B20/00—Purification of sugar juices
    • C—CHEMISTRY; METALLURGY
    • C13—SUGAR INDUSTRY
    • C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B20/00—Purification of sugar juices
    • C13B20/16—Purification of sugar juices by physical means, e.g. osmosis or filtration
    • C13B20/165—Purification of sugar juices by physical means, e.g. osmosis or filtration using membranes, e.g. osmosis, ultrafiltration

Definitions

  • the present invention relates to a process for producing sucrose from sugar beets.
  • the conventional beet sugar manufacturing process involves cleaning the beets, slicing them into cossettes, extracting juice from the cossettes by diffusion, purifying the juice by liming and carbonation, concentrating the juice by multiple effect evaporation, multi-stage boiling of concentrated juice in pans, separation, washing, and drying the sugar.
  • Juice extraction in the conventional process is done by allowing the sugar to diffuse through the natural cell walls of beets.
  • the cell walls allow sugars and other low molecular weight compounds to pass through but prevent the passage of high molecular weight compounds.
  • This selective diffusion process has two advantages. Retaining the high molecular weight compounds helps produce a high purity juice. It also reduces filtration difficulties that are caused by polysaccharides and proteins that comprise the high molecular weight compounds.
  • Lime serves many purposes in the juice purification process. It neutralizes the acidity of the juice and precipitates calcium salts of several organic and inorganic acids. The precipitate absorbs other impurities. The lime precipitate produces a porous mass, which facilitates subsequent filtration of juice.
  • the conventional diffusion process for juice extraction from beets has disadvantages. It has a long retention time, which encourages microbial growth, resulting in sugar loss and formation of undesirable compounds. It is difficult to increase the temperature of sliced cossettes quickly enough to prevent growth of micro-organisms. Typically the pulp remaining after diffusion is pressed and the press juice is introduced back into the diffuser. A significant portion of the high molecular weight compounds retained by the cell walls in the diffusion process is released in pressing to be mixed with the diffusion juice. This partially negates the advantages of the selective diffusion process.
  • the conventional liming process uses large quantities of lime, amounting to about 2.5% of the total weight of beets processed. Beet sugar plants operate lime kilns and transport limestone over long distances for this purpose.
  • the effluent from the liming-carbonation process consisting of used lime and separated impurities, is disposed as waste. Production of lime and disposal of liming effluent are costly operations. Disposal of liming effluent is becoming increasingly difficult and expensive in many communities.
  • EP 0126512 discloses a process for the recovery of disaccharides from disaccharides containing tuberous plants by mechanically reducing the tuberous plants to a mush, extracting the reduced material with water of less than 60°C, subjecting the extract first to an ultrafiltration and then to a demineralisation and finally concentrating the obtained solution.
  • the present invention relates to a process for producing sugar from sugar beets.
  • the process comprises the steps of (a) macerating beets or pieces thereof; (b) mechanically separating juice from the macerated beets by vacuum extraction at a temperature of at least 80°C; and (c) membrane filtering the separated juice, producing a retentate and a permeate.
  • This embodiment of the present invention makes use of mechanical means for separating juice from macerated beets, as opposed to the simple diffusion process that is used in prior beet processing technology to obtain juice from cossettes.
  • the maceration is done in an attrition mill. It is also preferred that vacuum extraction of juice is done on a moving porous filtration belt with countercurrent flow of macerated beets and water.
  • the pH of the vacuum extracted juice preferably is adjusted to at least about 7 by addition of sodium hydroxide.
  • the extracted juice is contacted with an agent selected from the group consisting of sulfur dioxide, sulfate salts, sulfite salts, bisulfite salts, and mixtures thereof, in an amount sufficient to adjust the pH of the extracted juice to no greater than about 8.
  • the membrane filtration can suitably be done with an ultrafiltration membrane, a nanofiltration membrane, or other types of membranes described herein.
  • the membrane filtration is cross-flow ultrafiltration, and is done at least about 80°C, and the pH of the permeate is at least about 7.
  • diafiltration filtrate also referred to herein as diafiltrate.
  • This diafiltrate preferably is combined with the membrane filtration permeate for further processing.
  • Another preferred option in the process is concentration of the permeate from the membrane filtration by reverse osmosis, thereby producing a concentrated solution. This concentrated solution is evaporated and sucrose is crystallized therefrom.
  • no lime and no carbon dioxide are contacted with the juice or the permeate.
  • a sucrose-containing feed juice that has been obtained from sugar beets is filtered through a first ultrafiltration membrane that has a first molecular weight cutoff.
  • This ultrafiltration step produces a first ultrafiltration permeate and a first ultrafiltration retentate.
  • the first ultrafiltration permeate is filtered through a second ultrafiltration membrane that has a second molecular weight cutoff that is lower than the first molecular weight cutoff.
  • This second ultrafiltration step produces a second ultrafiltration permeate and a second ultrafiltration retentate,
  • the second ultrafiltration permeate is nanofiltered through a nanofiltration membrane, thereby producing a nanofiltration permeate and a nanofiltration retentate.
  • the nanofiltration retentate has a higher concentration of sucrose on a dry solids basis than the feed juice introduced into the first ultrafiltration step, and can be used in evaporation and crystallization operations to produce crystals of white sugar.
  • the process can optionally include an additional step or steps to remove residual beet fibers and silt from the separated liquid (juice). This can be done by screening and/or filtration.
  • the screening or filtration removes at least 90 % by weight of all fibers and silt having a largest dimension of about 150 ⁇ m or greater, more preferably at least 90 % by weight of all fibers and silt having a largest dimension of about 50 ⁇ m or greater.
  • the first ultrafiltration membrane preferably has a molecular weight cutoff of at least about 2,000 daltons and a pore size no greater than about 0.1 microns. More preferably, it has a molecular weight cutoff of about 4,000-200,000 daltons.
  • the first ultrafiltration permeate preferably has a color of about 3,000-10,000 icu. (All color values given herein are determined on an ICUMSA scale.)
  • the process of the present invention can be operated at a number of different process conditions.
  • the feed juice can be at a temperature of about 140-200 °F (60-93 °C) during the first ultrafiltration, more preferably about 160-185 °F (71-85 °C).
  • the second ultrafiltration membrane preferably has a molecular weight cutoff of about 500-5,000 daltons, more preferably about 1,000-4,000 daltons.
  • the second ultrafiltration is performed in two stages, the first stage using an ultrafiltration membrane having a molecular weight cutoff of about 3,500-4,000 daltons, and the second stage using an ultrafiltration membrane having a molecular weight cutoff of less than about 3,500 daltons.
  • the second ultrafiltration permeate preferably has a color no greater than about 4,000 icu, more preferably no greater than about 2,500 icu.
  • Diafiltration is used herein to mean ultrafiltration that employs added water in the feed to help flush sucrose through the membrane.
  • the first ultrafiltration retentate is diafiltered through at least a first diafiltration/ultrafiltration membrane. This produces a first diafiltration permeate and a first diafiltration retentate. The first diafiltration permeate is then combined with the first ultrafiltration permeate and filtered through the second ultrafiltration membrane.
  • the retentate from the second ultrafiltration can be diafiltered through at least a second diafiltration/ultrafiltration membrane.
  • This second diafiltration step produces a second diafiltration permeate and a second diafiltration retentate.
  • the second diafiltration permeate is then combined with the second ultrafiltration permeate and subsequently filtered through the nanofiltration membrane.
  • the retentates from the first and second ultrafiltrations (or diafiltrations) and the nanofiltration permeate can be combined to produce molasses.
  • This combined stream may need to be concentrated by evaporation of water.
  • the nanofiltration retentate is purified by electrodialysis, thereby producing a electrodialyzed juice and an electrodialysis residue, and then the electrodialyzed juice is purified by ion exchange, thereby producing a purified juice.
  • the nanofiltration retentate is purified by electrodialysis, thereby producing a electrodialyzed juice and an electrodialysis residue, and then the electrodialyzed juice is purified by ion exchange, thereby producing a purified juice.
  • no lime and no carbon dioxide are contacted with any of the permeates.
  • the nanofiltration removes ash (including mono- and divalent cations), invert, organic acids, nitrogenous material and other low molecular weight organic or charged compounds.
  • the nanofiltration and the optional electrodialysis and/or ion exchange preferably remove at least about 65 % by weight of the Ca, Mg, K, Na and their associated inorganic and organic anions that are present in the second ultrafiltration permeate.
  • the ion exchange replaces remaining divalent cations such as calcium and magnesium with monovalent cations such as potassium and sodium.
  • the nanofiltration retentate has a lower concentration of divalent cations on a dry solids basis than the second ultrafiltration permeate.
  • the nanofiltration permeate will contain a large percentage of the impurities that were present in the feed juice.
  • the nanofiltration permeate will comprise at least about 30% by weight on a dry solids basis of the ash, at least about 30% of the invert, and at least about 25% of the betaine present in the feed juice.
  • the purified juice i.e., after nanofiltration and any electrodialysis and/or ion exchange
  • the purified juice preferably has an ash concentration of no greater than about 2.5 % by weight on a dry solids basis, more preferably no greater than about 2 %, most preferably no greater than about 1.0 %.
  • the present invention can achieve two crystallizations of white sugar from the concentrated syrup, as opposed to one in typical prior art beet processes.
  • a mother liquor will remain after one or more crystallizations of white sugar from the concentrated syrup.
  • This mother liquor can be recycled to one of the ultrafiltrations.
  • this recycle stream can be further purified to reduce its raffinose content.
  • the process can optionally include sulfitation of one or more process streams.
  • at least one aqueous stream selected from the group consisting of the feed juice, the first ultrafiltration permeate, the second ultrafiltration permeate, the nanofiltration retentate, and the evaporator feed can be contacted with an agent selected from the group consisting of sulfur dioxide, sulfite salts, bisulfite salts, metabisulfite salts, dithionites, and mixtures thereof, in an amount sufficient to provide an equivalent concentration of sulfur dioxide in the stream of at least about 100 ppm.
  • the process of the present invention eliminates the need for a lime kiln, lime quarries and all associated equipment, processes, products, by-products and waste products.
  • the present invention results in a drastic reduction of waste products that cause environmental pollution.
  • the conventional process produces a filter cake that comprises products of the liming process and impurities removed from the juice. This cake is disposed into ponds or landfills.
  • the proposed process completely eliminates the need for disposal of such materials.
  • the present invention allows elimination of the carbonation process, which is a major source of atmospheric pollution in beet sugar plants.
  • the present invention provides a cost-effective way of reducing the ash content of the beet juice or syrup, preferably to about 2 % or less (on a dry solids basis), more preferably to about 1.5 % or less, most preferably to about 1 % or less.
  • This reduction in ash content is important because it allows a second strike of sucrose crystals from the syrup.
  • ash contents in the range of 3.5 % made it practically impossible to have more than one strike of sucrose crystals.
  • the present invention can eliminate the need for desugarization of molasses streams.
  • the efficient membrane filtration steps prevent excessive amounts of sucrose from entering the molasses streams in the first place.
  • the present invention provides an economical and reliable method for removing color-causing materials from beet juice. It also can reduce the formation of undesirable crystalline forms due to the presence of excessive amounts of raffinose.
  • the present invention provides an improved method for obtaining sucrose from sugar beets.
  • One embodiment of the invention is represented in Figure 1.
  • Beets received from the field are kept in a storage area 10. Fresh beets are typically used in the process, but frozen beets can also be used. Beets from the storage 10 area are flumed to a conventional beet washing apparatus 12, in which dirt is removed from the exterior of the beets. Washed beets exiting the washing apparatus pass through a conveyor 14, where water is removed. Wash water 18 and flume water 16 streams collected from this apparatus are sent to waste water treatment ponds 20.
  • the washed beets 21 are carried by conveying apparatus 22 to cutting apparatus 24, such as a hammer mill or slicer, in which the beets are cut into pieces, for examples pieces having an average size of about one inch thickness.
  • cutting apparatus 24 such as a hammer mill or slicer
  • the stream of beet pieces 26 from the slicer (or alternatively the whole beets 21) are fed to macerating apparatus 28.
  • the macerating apparatus can comprise, for example, one or more hammer mills (fixed blade type being the preferred option) that uses a set of rotating blades mounted on a horizontal shaft which forces the beet material through a discharge screen.
  • Another macerating apparatus can comprise one or more attrition mills that use discs as the primary attrition device.
  • the discs preferably have grooves therein to facilitate maceration, and the discs can be horizontal or vertical in positioning.
  • Disc-type attrition mills are presently preferred over hammer mills, although it is possible to use both in series (e.g., hammer mill followed by disc attrition mill).
  • extracted juice 38 or water 34 is fed to the macerator 28 to facilitate discharge of macerated beets and/or to control the temperature of the equipment.
  • the stream of macerated beets 30 is fed to a vacuum juice extraction apparatus 32.
  • This apparatus can comprise a horizontal, porous, moving belt that is subjected to a vacuum from the bottom. Macerated beets are introduced as a uniform layer at one end (the feed end) 33 of the belt. A clean water stream 34 is introduced at the opposite or discharge end 35 of the belt.
  • a stream of juice 36 is reintroduced over the belt, preferably at several locations.
  • This method of countercurrent filtration produces a pulp stream 68 with low sugar content and an extracted juice stream 38 with high sugar content.
  • the countercurrent vacuum filtration process is carried out at an elevated temperature of about 80°C to control microbial growth and to improve the extraction of juice.
  • the pulp 68 leaving the juice extractor 32 has a very low sucrose content but a high water content. It is pressed in a screw press 70 to extract a dilute press juice 72 which contains about 1% dissolved solids and about 99% water. The dissolved solids comprise about 50% sucrose and 50% non-sugars.
  • This dilute press juice 72 is raised to a temperature of about 80°C in a heater 74 and then is returned to the juice extractor 32 as stream 36. Pressed pulp 76 is used as animal feed, with or without further drying.
  • the extracted juice 38 is sent to tank 41 and can optionally be sulfitated by the addition of sulfur dioxide, or sulfite or bisulfite salts in a stream 40, e.g. sulfur dioxide gas or aqueous ammonium bisulfite at about 65% concentration.
  • sulfur dioxide or sulfite or bisulfite salts
  • the residual level of sulfur dioxide in the juice after sulfitation is at least 100 ppm.
  • the sulfitation can take place at the time of slicing, macerating, juice extraction, or other points in the process, as an alternative to or in addition to the particular sulfitation step in this embodiment. This sulfitation will prevent the color increase that can otherwise take place during subsequent membrane filtration and evaporation operations.
  • Other antioxidants may also be used.
  • the juice is then neutralized by the addition of aqueous sodium hydroxide 42, preferably to a pH of at least 7, in neutralization tank 43.
  • aqueous sodium hydroxide 42 preferably to a pH of at least 7, in neutralization tank 43.
  • This pH adjustment helps prevent the inversion of sugars which takes place at elevated temperatures.
  • Other chemicals may be also be used for pH adjustment, e.g. liquid potassium hydroxide or granular sodium carbonate.
  • the juice extracted from the macerated beets by the countercurrent filtration process comprises about 0.2% suspended solids, about 14% dissolved solids, and about 84% water.
  • the dissolved solids comprise about 85% sucrose and 15% non-sugars.
  • the temperature of the extract is about 80°C and its pH is at least 7.
  • the treated juice can then be passed through a heater 44 to increase its temperature to about 80°C.
  • the heated juice is then processed by membrane filtration 46, preferably by cross-flow ultrafiltration, to separate high molecular weight compounds from sucrose solution.
  • Ultrafiltration produces an ultrafiltrate (also referred to as permeate or clarified juice) 48 which is about 12% dissolved solids and about 88% water.
  • the dissolved solids comprise about 90% sucrose and 10% non-sugars.
  • the ultrafiltrate 48 preferably has a temperature of about 80°C and its pH is at least 7.
  • the permeate from ultrafiltration has a sucrose purity equivalent to the thin juice produced by the conventional beet process, which is around 90%.
  • Ultrafiltered juice may contain a higher level of invert sugar and/or a lower level of macromolecular compounds than the conventional thin juice.
  • Invert sugars in the ultrafiltered juice will primarily end up in the molasses without reducing sucrose recovery drastically. This is an advantage compared to the conventional liming process, which sends reaction products of lime and invert sugars to the effluent disposal system. Lower levels of macromolecular compounds result in juice with lower viscosity, which has more favorable sugar boiling characteristics.
  • Ultrafiltration produces a juice with reduced color.
  • the extracted juice 38 typically has color value over 100,000 on a ICUMSA scale.
  • the ultrafiltrate 48 typically has a color value below 2,000 on the same scale. This is equivalent to or better than the color value of thin juice prepared by the conventional method. Lower color in combination with lower viscosity result in an easier sugar boiling process. The results are higher sugar extraction, more efficient sugar boiling, and lower sugar loss to molasses.
  • membrane configurations can be used in the present invention, including for example spiral, hollow fiber, and tubular membranes.
  • Membranes suitable for this separation process should have two unique characteristics. They should have high permeability to water and sucrose but have low passage of colorants and other macromolecular compounds. Tight ultrafiltration membranes with a molecular weight cutoff between about 1,000 and 10,000 and loose nanofiltration membranes with NaCl rejection of about 10% are well suited for this application. Membranes that have a negative surface charge are preferred since most compounds to be rejected are negatively charged.
  • the retentate 50 from the ultrafiltration process contains mostly suspended and dissolved impurities. It also contains a significant amount of sucrose. In order to recover at least some of this sucrose, the retentate is diafiltered through a membrane system 52 with addition of water 54. This diafiltration extracts most of the sugar left in the ultrafiltration retentate.
  • the diafiltrate 56 contains about 3% dissolved solids and about 97% water.
  • the dissolved solids in the diafiltrate comprise about 88% sucrose and 12% non-sugars.
  • the temperature of the diafiltrate is about 80°C and its pH is above 7.
  • the retentate 58 of the diafiltration process contains about 5% suspended solids, 3% dissolved solids and about 87% water. This is concentrated by evaporation and used as animal feed, with or without mixing with pressed pulp.
  • the ultrafiltrate 48 and diafiltrate 56 are combined to form a composite product stream 60.
  • the composite product stream (also referred to as purified juice) contains about 11 % dissolved solids and about 89% water.
  • the dissolved solids comprise about 90% sucrose and 10% non-sugars.
  • a reverse osmosis membrane system 62 may be used for pre-concentration of the purified juice stream. This is another cross-flow membrane process that is less energy intensive and more economical for pre-concentration of dilute sucrose solutions than the conventional process steps.
  • the product 64 of the reverse osmosis system contains about 20% dissolved solids and about 80% water. The dissolved solids comprise about 90% sucrose and 10% non-sugars.
  • the permeate 66 of the reverse osmosis is high quality water. A portion 34 of this water is used in the countercurrent vacuum filtration process 32 and remainder in other plant applications, such as water feed 54 to the diafiltration process 52.
  • the temperature of the pre-concentrated sucrose solution 64 is then raised in a heater 80 and subsequently the remaining water is removed in evaporators 82.
  • Sucrose is crystallized as in conventional processes.
  • Beet slicing apparatus 24 and macerating apparatus 28 are commercially available from suppliers such as H. Putsch GmbH & Company (Hagen, Germany), Maguin Company (Charmes, France), Dakota Machine Inc. (West Fargo, North Dakota), and The Fitzpatrick Company (Elmhurst, Illinois). Suitable vacuum belt juice extraction apparatus is available from EIMCO Company (Salt Lake City, Utah), and Dorr-Oliver (Milford, Connecticut). Centrifugal extraction apparatus is available from Western States Machine Company (Hamilton, Ohio) and Silver-Weibull (Hasslehom, Sweden). Suitable membrane filtration systems are available from suppliers such as CeraMem Corp. (Waltham, Massachusetts), Koch Membrane Systems, Inc. (Wilmington, Massachusetts), and Osmonics, Inc. (Minnetonka, Minnesota).
  • Suitable variations include reverse osmosis before ultrafiltration, sulfitation after ultrafiltration, and sterilization of the macerated beets by chemical or physical means.
  • Separate treatment of the press juice 72 instead of returning it to the countercurrent vacuum filtration process is another alternative. It would also be possible to include treatment with some amount of lime and/or carbonation. However, it is presently preferred to operate the process without the use of either lime or carbonation.
  • Chromatographic separation could be used for further purification in this process. Chromatographic separation requires juice pretreatment and juice softening. Since the juice from the present process has been passed through membrane filtration and no lime has been added, it would be excellent feed to chromatographic separation.
  • membrane separation in the proposed process could allow for separation of sucrose from other beet juice components such as invert sugars and oligosaccharides.
  • Leaching of macerated beets has been demonstrated to be capable of achieving 99.8% recovery of sugars in six stages, each using fresh water.
  • Ultrafiltration of juice has also been demonstrated to be capable of achieving 99.8% sugar recovery in six stages of diafiltration.
  • this degree of extraction may be too ambitious for an industrial process since it involves excessive use of dilution water, which has to be removed eventually for recovery of sugar.
  • a mass balance of a process according to the present invention was prepared based on an input of 1,000 units of beets with 78% water, 17% RDS and 89% sucrose purity, and an assumed sugar recovery of about 99.5% in both extraction and diafiltration operations.
  • Figure 2 shows a flow diagram of this embodiment of the process with the mass balance. The numbers in bold type are assumed based on experimental data and other available information. All other numbers are determined using constitutive and conservation relations.
  • EJ refers to extracted juice
  • UFP ultrafiltration permeate
  • UFR ultrafiltration retentate
  • ''DFP'' refers to diafiltration permeate
  • DFR diafiltration retentate
  • MP refers to mixed permeate
  • NSDS non-sugar dissolved solids.
  • beets are macerated with juice from the second stage of the extractor.
  • Macerated beets are fed to the first stage of the extractor and juice from this stage is fed to the ultrafiltration system. Pulp from the first stage moves through several stages of the extractor until nearly all the sugar (99.5%) is extracted.
  • Fresh water is introduced in the last stage of the extractor. Extracted juice is processed by ultrafiltration to recover 90% of the juice as ultrafiltrate. The retentate is diafiltered five times its volume of fresh water. Combined Ultrafiltration and diafiltration recover about 99.5% of the sugar in the feed.
  • process of the present invention can be operated in batch mode, it is especially well suited for continuous operation.
  • Macerated beet pulp was mixed with water and pressed in cloth bags to produce a sample of expelled juice, This sample was treated with sodium hydroxide, heated and used in a set of ultrafiltration trials. Two different spiral ultrafiltration membranes were used in the trial, a Hydranautics model NTR7410 membrane and a Koch model HFK131 membrane. The trials produced satisfactory flux rates, higher than comparable trials with conventional beet diffusion juice.
  • Table 2 Ultrafiltration of Expelled Juice - Trial Parameters and Fluxes Trial No. Pretreatment Membrane Type Trial Conditions Trial Results Temp. °F (°C) Pressure PSIG (kPa) Recovery (%) Flux LMH 1 aOH-Heat Spiral 150 (66) 70 (483) 86 30 2 NaOH-Heat Spiral 150(66) 70 (483) 86 25
  • a beet maceration trial was conducted using a Bauer atmospheric disc refiner. This machine has two 12 inch (30 cm) discs with adjustable gap, one disc stationary and other disc driven by a 60 hp (45 kW) motor. About 20 kg of beets were used in the trial. Beets were chopped to 3/4 inch (1.9 cm) pieces to suit the screw feeder.
  • the pulp from the first pass was processed through the machine again in a second pass.
  • the gap between the discs was set to about 10 mil (0.25 mm) for this pass.
  • the macerated pulp was pressed in the bladder press at 20 psi (138 kPa) for about 15 minutes.
  • Table 5 Material Concentration Juice from bladder press 7.6 Brix Press cake from bladder press 21.0% dry solids (The lower solids content in the pass 2 bladder press cake was due to its higher thickness.)
  • the macerated beet fibre stream from the first centrifuge was fed to a system of 50 micron screens operating in a counter current fashion, and finally to a second Mercone centrifuge fitted with a 250 micron screen.
  • This second centrifuge desweetened the fibre providing a residual beet fibre contained 5.7% sugar and 88% water.
  • Juice was recycled from the second centrifuge and counter-current through the system of screens to the first centrifuge at 3 - 5 gallons / minute (11-19 L/min).
  • About 250 ppm on beets of antifoam oil (KABO 580) was added to the juice, while hot water was fed to the second centrifuge at 1 gallon / minute (4 L/min).
  • the juice was adjusted to 70 °C, pH adjustment was carried out by adding sodium hydroxide solution to the maceration stage, and the final juice was pH trimmed as necessary.
  • the final juice from the macerated beets was at 13.2 RDS (refractometric dry solids) and pH 6.4 (measured at ambient temperature).
  • the apparent purity (Pol/Brix) was 82.6; conductivity ash 3.9% and colour 29,900 icu. It contained 0.6% fibre.
  • the juice from Example 6a was fed to the first ultrafiltration.
  • the inlet pressure averaged 100 psi (689 kPa), the outlet 63 psi (434 kPa), and the cross flow rate was 537 litres / minute.
  • the permeate flow rate was 2.6 litres / minute (corresponding to 60 Litres / square meter / hour).
  • the permeate was 11.0 RDS; pH 6.5; apparent purity 83.8; colour 4705 icu. and ash 4.9%.
  • the retentate was 11.1 RDS; 74.4 apparent purity; 5.1% ash and 60,800 icu colour.
  • the permeate from the first ultrafiltration system was fed at about 70 °C to a second ultrafiltration system which comprised two 4 inch (10 cm) spiral Osmonics GN membranes having a molecular weight cut off of 3,500 Daltons, with a surface area of 12 square meters.
  • the inlet pressure averaged 65 psi (448 kPa), the outlet 50 psi (345 kPa).
  • the total permeate flow rate averaged 1.4 litres / minute giving 7 Litres / square meter / hour.
  • the permeate was 8.6 RDS; pH 7.0; apparent purity 83.6; colour 1666 icu, and conductivity ash 4.9% (5.4% sulphated ash).
  • the retentate was 14.2 RDS; 83.3 apparent purity; conductivity ash 5% and 13,800 icu colour.
  • the permeate from the second ultrafiltration membrane was passed over a cation exchange resin (Purolite C155S) in the sodium form.
  • the flow was 2.4 litres / minute and this was passed over 90 litres of resin at 1.6 Bed volumes / hour and at 70°C.
  • the product was 7.1 RDS, at pH 6.4, the apparent purity was 83.5; colour 1505 icu, and conductivity ash 5.6% (5.2% sulphated ash).
  • the ionic composition of the resin input and output streams was: Table 9 Ca Mg K Na Cl PO4 SO4 Oxalate Feed 0.003% 0.085% 0.97% 0.91 % 0.49% 0.28% 0.091% 0.44% Product 0.001% 0.038% 0.87% 1.000% 0.52% 0.30% 0.089% 0.37%
  • the resin product stream was treated by nano filtration with 3 stages of Desal 5DL membranes.
  • the total membrane surface was 18 square metres, and the inlet pressure 450 psi (3013 kPa), and temperature 65°C.
  • the feed flow was 2.6 litres / min and the retentate flow 1.0 litres / min.
  • Diafiltration water was introduced between the stages at 0.3 litres / min.
  • the retentate (product) stream was 25.4 RDS; 88.3 apparent purity; colour 1154 icu and 2.9% ash.
  • the permeate was 1.8 RDS ; 12.0 apparent purity; 3083 colour and about 20% ash.
  • the product stream from the nano filtration was evaporated to give a syrup at 70.5 Brix.
  • Approximately 1ml / minute of ammonium bisulfite (ABS) solution was added to the feed juice to the evaporator.
  • ABS was a 65% stock solution diluted 1:1.
  • the evaporator was a single effect APV plate and frame unit, and was operated at 8 psia (55 kPa absolute) and the syrup temperature was about 85°C.
  • the feed flow rate was 1 litre / minute at 25.4 brix.
  • the liquor produced by the evaporator was crystallized under vacuum to give white sugar with colour 10.2 icu and a conductivity ash of 0.009%.
  • the crystallisation was carried out in batch mode, in a crystalliser containing 50 litres of massescuite.
  • the crystalliser was a pilot unit manufactured by Pignat of Genas, France. Crystallisation pressure and temperature were 20 in Hg abs (68 kPa absolute) and 70 - 75°C and crystallisation took 2 hours.
  • the massecuite formed by crystallisation was centrifuged on a 2 foot basket centrifuge using a perforated basket.
  • the mother syrup (separated by centrifugation) had an apparent purity of 81.8% and a colour of 2988 icu.
  • a second ultrafiltration stage UF2 similar to that described in example 6c above but comprising two 4 inch (10 cm) spiral Osmonics GN (MWCO 3500 Daltons) and two 4 inch (10 cm) spiral Osmonics GM membrane (MWCO 3000 Daltons) modules was used to treat juice from a first stage of ultrafiltration. This juice was originally derived from macerated beets as described above. The modules ran at input pressures averaging 160 and 250 psi (1103 and 1724 kPa) respectively and delivered an overall 2.5 litres / min of permeate (pH 6.5, 9 RDS and 1890 colour).
  • the permeate was treated with a cation exchange resin (Purolite PCR) in the potassium form at 70°C and 0.9 Bed Volumes / hour.
  • the product was at pH 7.0, 8.9 RDS, 85.1 purity and 1958 colour.
  • the input and output compositions (% on dry solids) were: Table 11 Ca Mg K Na Ash Resin feed 0.006% 0.158% 1.14% 0.67% 5.4% Resin product 0.006% 0.003% 3.39% 0.06% 7.8%
  • the product from the ion exchange resin in the potassium form in Example 7 was treated by nano filtration (operated as in Example 6e above).
  • the product (retentate) was 23 RDS, 89.5% purity (by HPLC), 4.5% as sulphated ash and 1800 icu colour. It was treated by electrodialysis in a stack comprising 40 cationic/anionic membrane pairs; each pair had 0.1 m 2 of membrane surface.
  • the membranes used were manufactured by Tokuyama Corp of Japan, the anion membrane was AE506sb, and the cation membrane was CMXsb.
  • the stack operated at 45 - 55°C; with 18-30 volts and a current of 2 - 3 amps.
  • the anolyte and catholyte systems contained dilute sulphamic acid (20 mS/cm conductivity) which circulated through the stack at 3 gpm (11 L/min). The stream being treated circulated at 8 - 10 gpm (30-38 L/min), and flowed through the whole system at about 1 litre / minute. The concentrate stream was 0.5% sodium chloride solution. The electrodialysed product stream was at 94.4% purity (by HPLC) and had 2.2% sulphated ash (calculated from the cation composition as shown below where the ionic composition of the feed and product streams is expressed as % ions on solids. Table 12 Ca Mg K Na Ash Feed 0.002% 0.009% 1.86% 0.104% 4.5% Product 0.001% 0.003% 0.88% 0.079% 2.2%
  • the membrane used was a 4 inch (10 cm) Osmonics JY spiral having a membrane area of 4.8 square meters and a cut off of 100,000D.
  • the temperature of the juice was 140°F (60°C) and the inlet and outlet pressures were 50 psi and 30 psi (345 and 207 kPa) respectively.
  • the feed rate was 3.6 litres per minute, and permeate and retentate flows were both 1.8 litres per minute at 13 and 14.2 RDS respectively, giving a flux rate of 22.5 litres / square meter / hour at a concentration factor of x2.
  • the feed colour was 1232 iu and the permeate colour was 6475 iu. This juice can be further processed to white sugar using steps 6c, 6d, 6e, and 6f.
  • the juice comprising a mixture of the mother liquor from white sugar crystallisations and the retentate from a second ultrafiltration can be evaporated to 60 RDS and passed at a rate of 0.9 litres/hour over a simulated moving bed separating system, containing 5.8 litres of resin distributed among 10 cells. Water can be injected at 4 litres per hour and the system operated at a temperature of 70 °C. Three fractions can be collected from the system containing respectively, most of the organics; most of the sucrose; and most of the raffinose plus other organic materials. Typical properties of each of these fractions are given in the tables below.
  • the sucrose fraction obtained can be 96% pure and represent a recovery of 92.5% of the sucrose input.
  • the mother syrup from the crystallisation of a first strike of white sugar (colour 3147 icu at 83.1% apparent purity) was crystallised under vacuum to give a second crop of white sugar with colour 20 icu and a conductivity ash of 0.01 %.
  • the crystallisation was carried out in batch mode in a crystalliser containing 50 litres of massecuite.
  • the crystalliser was a pilot unit manufactured by Pignat of Genas, France. Crystallisation pressure and temperature were 20 inch Hg abs and 70 - 75 °C, and crystallisation took about 2 hours.
  • the massecuite formed by crystallisation was centrifuged on a 2 foot (0.6 m) basket centrifuge using a perforated basket.
  • the mother syrup (separated by centrifugation) had an apparent purity of 81.1% and a colour of 4155 icu.
  • Beet juice from a factory diffuser (colour about 4200 icu) was fed to the first centrifuge (with a 150 micron screen) to remove residual fibres, and heated to 70°C. It was aerated vigorously, screened (50 micron) and adjusted with sodium hydroxide to pH 8.0. The resulting juice was 17.5 RDS, apparent purity 85.1, colour 16400 and conductivity ash 5.3. It contained 0.09% fibre.
  • This juice was fed at 73 °C to the first ultrafiltration: an Osmonics PW, 4 inch (10 cm) diameter membrane module with spiral elements having a molecular weight cut off of 10 - 15,000 Daltons, and a surface area of 4.3 m 2 .
  • the inlet pressure averaged 66 psi (455 kPa), the outlet 45 psi (310 kPa), and the cross flow rate was 193 litres / minute.
  • the permeate flow rate was 1.9 litres / minute (corresponding to 26 litres / square meter / hour).
  • the permeate was 15.5 RDS; apparent purity 85.6; colour 6697 icu, and ash 5.3%.
  • the retentate was 12.5 RDS and 83.4 apparent purity. Diafiltration of the retentate using a PCI 20,000 Dalton molecular weight cut off tubular membrane produced a further 1.6 litres / min of permeate at 7 RDS. The permeates were mixed.
  • the combined permeates from the first ultrafiltration system were fed at 65 °C to a second ultrafiltration system using two Osmonics GK and two Osmonics GE membrane 4 inch (10 cm) spiral modules. These membranes have 2000 Dalton and 1000 Dalton molecular weight cut offs respectively. It ran at input pressures averaging 250 psi (1724 kPa) and delivered a total of 2.2 litres / min of permeate (13.5 RDS, 85.0 apparent purity, 6.5% conductivity ash and 3297 colour). The retentate was 21.4 RDS and 83.8 apparent purity. The total membrane area was 24 square meters and the average flux rate was 5.5 litres/square meter /hour
  • the permeate from the second ultrafiltration membrane system was treated by nano filtration with 2 stages of 4 inch (10 cm) diameter Desal DS5 membranes.
  • the total membrane surface was 12 square metres, the inlet pressure 450 psi (3103 kPa), and temperature 150 °F (66 °C).
  • the feed flow was 0.75 gpm (2.5 L/min) and the retentate flow 0.3 gpm (1 L/min).
  • Diafiltration water was introduced into the second stage at 2.75 gph.
  • the retentate (product) stream was 24.9 RDS; 90.6 apparent purity (90.8% by HPLC); colour 2802 icu and 4.2% conductivity ash.
  • the permeate was 5.2 RDS and 38.3 apparent purity.
  • the nano filtration retentate from Example 13c was treated by electrodialysis in a stack comprising 40 cationic/anionic membrane pairs, each pair had 0.1 m 2 of membrane surface.
  • the stack operated at 45 - 55 °C; with 18 - 30 volts and a current of 2 - 3 amps.
  • the anolyte and catholyte systems contained dilute sulphamic acid (20 mS/cm conductivity) which circulated through the stack at 3 gpm (11 L/min).
  • the stream being treated circulated at 8 gpm (30 L/min), and the equipment was operated in a batch mode.
  • the stack was operated at 40 - 50°C; with 12 - 23 volts and a current of 3 amps.
  • the feed and product ionic compositions were: Table 14 % of Ions on Solids % Ash Ca Mg K Na Cl PO4 SO4 Oxalate Feed 0.001 0.12 0.65 0.61 0.049 0.146 0.523 0.628 3.9 Product 0.003 0.02 0.19 0.19 0.021 0.046 0.061 0.073 1.2
  • the product from electrodialysis (after adding about 900 ppm of SO 2 as an ammonium bisulphite solution) was evaporated to give a syrup at 69 Brix (colour 3060 icu).
  • the evaporator was a single effect APV plate and frame unit, and was operated at 8 psia (55 kPa abs) and the syrup temperature was about 85°C.
  • the feed into the evaporator was 1 litre / minute at 24 Bx.
  • the evaporated syrup was crystallised under vacuum to give a white sugar with 17.3 icu colour and a conductivity ash of 0.007%.
  • the crystallisation was carried out in batch mode in a crystalliser containing 50 litres of massecuite.
  • the crystalliser was a pilot unit made by Pignat of Genas, France. Crystallisation pressure and temperature were 20 in Hg abs (68 kPa abs) and 70 - 75°C and crystallisation took 2 hours.
  • the massecuite formed by crystallisation was centrifuged on a 2 foot (0.6 m) basket centrifuge using a perforated basket.
  • the mother syrup (separated by centrifugation) had an apparent purity of 80.3% and a colour of 5380 icu.
  • Example 13e The mother syrup produced by the methods of Example 13e was further crystallised in the Pignat crystalliser at 20 in Hg abs (68 kPa) and 70 - 75°C over 3 hours.
  • the massecuite was centrifuged on a 2 foot (0.6 m) basket centrifuge and gave a second sugar of color 40 iu and 0.019 ash.
  • Example 14a The work in Example 14a was repeated, but feeding the oxidation with beet diffuser juice that had been heated and aerated as described in Example 13a.
  • the feed colour was 12,123 icu.
  • Peroxide treatment raised this to 14,473 icu and ultrafiltration gave a permeate at 2707 icu.
  • the juice comprising a mixture of the mother liquor from white sugar crystallisations and the retentate from a second ultrafiltration can be evaporated to 60 RDS and passed at a rate of 1.0 litres/hour over a simulated moving bed separating system, containing 5.8 litres of resin distributed among 10 cells. Water can be injected at 4 litres per hour and the system operated at a temperature of 70 °C. Three fractions were collected from the system containing respectively, most of the organics; most of the sucrose; and most of the raffinose plus other organic materials. Typical properties of each of these fractions are given in the tables below.
  • the sucrose fraction obtained typically is 96.5% pure and represents a recovery of 90.5% of the sucrose input.
  • 500 grammes of the mother liquor from the first crystallisation of white sugar (at about 75 RDS, and containing 2.6% raffinose on solids) was diluted to 30 RDS with water.
  • the pH was adjusted to 5.0 by adding dilute sulphuric acid and the solution temperature brought to 50 °C.
  • 2.5 x 10 7 units of pelleted alpha galactosidase enzyme were added (12.2 grammes) and the solution stirred at 50 °C for 2 hours.
  • the resulting juice was analysed and found to contain 0.9% raffinose on solids.
  • the mother syrup from the crystallisation of a first strike of white sugar (colour 4094 icu at 80.8% apparent purity) was crystallised under vacuum to give a second crop of white sugar with colour 28 icu and a conductivity ash of 0.024%.
  • the crystallisation was carried out in batch mode in a crystalliser containing 50 litres of massecuite.
  • the crystalliser was a pilot unit manufactured by Pignat of Genas, France. Crystallisation pressure and temperature were 20 inch Hg abs (68 kPa abs) and 70 - 75 °C, and crystallisation took about 2 hours.
  • the massecuite formed by crystallisation was centrifuged on a 2 foot (0.6 m) basket centrifuge using a perforated basket.
  • the mother syrup (separated by centrifugation) had an apparent purity of 77,4% and a colour of 5807 icu.

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Claims (25)

  1. Verfahren zur Herstellung von Zucker aus Rüben, mit den folgenden Schritten:
    (a) Aufschluß von Rüben oder Rübenstücken;
    (b) mechanisches Abtrennen von Saft von den aufgeschlossenen Rüben durch Vakuumextraktion bei einer Temperatur von mindestens 80°C; und
    (c) Membranfiltration des abgetrennten Safts, wodurch ein Filterrückstand bzw. Retentat und ein Permeat erzeugt werden.
  2. Verfahren nach Anspruch 1, wobei die Rüben oder Rübenstücke im Schritt (a) in einer Reibmühle oder Hammermühle aufgeschlossen werden.
  3. Verfahren nach Anspruch 1, wobei das mechanische Abtrennen von Saft auf einem sich bewegenden porösen Vakuumfilterband im Gegenstrom von aufgeschlossenen Rüben und Wasser erfolgt.
  4. Verfahren nach Anspruch 1, wobei die Membranfiltration mit einer Ultrafiltrationsmembran oder einer Nanofiltrationsmembran oder mit beiden erfolgt.
  5. Verfahren nach Anspruch 4, wobei die Membranfiltration eine bei mindestens 80°C durchgeführte Kreuzstromfiltration aufweist und der pH-Wert des Permeats mindestens gleich 7 ist.
  6. Verfahren nach Anspruch 1, wobei die Membranfiltration von Schritt (c) aufweist:
    Filtern des abgetrennten Safts durch eine erste Ultrafiltrationsmembran mit einer ersten Molekulargewichtsgrenze, wodurch ein erstes Ultrafiltrationspermeat und ein erstes Ultrafiltrationsretentat erzeugt werden;
    Filtern des ersten Ultrafiltrationspermeats durch eine zweite Ultrafiltrationsmembran mit einer zweiten Molekulargewichtsgrenze, die niedriger ist als die erste Molekulargewichtsgrenze; wodurch ein zweites Ultrafiltrationspermeat und ein zweites Ultrafiltrationsretentat erzeugt werden; und
    Filtern des zweiten Ultrafiltrationspermeats durch eine Nanofiltrationsmembran; wodurch ein Nanofiltrationspermeat und ein Nanofiltrationsretentat erzeugt werden, wobei das Nanofiltrationsretentat eine höhere Saccharosekonzentration auf Trockenstoffbasis aufweist als der abgetrennte Saft im Schritt (b).
  7. Verfahren nach Anspruch 6, wobei das Nanofiltrationsretentat durch Elektrodialyse gereinigt wird, wodurch ein elektrodialysierter Saft und ein Elektrodialyserückstand erzeugt werden; der elektrodialysierte Saft durch Ionenaustausch erweicht wird, wodurch ein erweichter gereinigter Saft entsteht; und die Nanofiltration, Elektrodialyse und der Ionenaustausch mindestens 65 Gew.-% Ca, Mg, K, Na und deren zugehörige anorganische und organische Anionen entfernen, die in dem zweiten Ultrafiltrationspermeat vorhanden sind.
  8. Verfahren nach Anspruch 6, wobei der pH-Wert des Safts durch Zusatz einer Base vor der ersten Ultrafiltration auf 6 - 8 eingestellt wird.
  9. Verfahren nach Anspruch 6, das ferner den Schritt zum Entfernen von restlichen Rübenfasern und Schlamm aus dem Saft vor der ersten Ultrafiltration durch mindestens ein Verfahren aufweist, das aus der Gruppe ausgewählt ist, die aus Sieben und Filtern besteht, wobei das Sieben oder Filtern mindestens 90 Gew.-% aller Fasern und des Schlamms mit einer größten Abmessung von 150 µm oder mehr entfernt.
  10. Verfahren nach Anspruch 6, wobei das erste Ultrafiltrationsretentat einer Diafiltration durch mindestens eine erste Diafiltrations-/Ultrafiltrationsmembran ausgesetzt wird, wodurch ein erstes Diafiltrationspermeat und ein erstes Diafiltrationsretentat erzeugt werden; und wobei das erste Diafiltrationspermeat durch eine zweite Ultrafiltrationsmembran gefiltert wird, und wobei das zweite Ultrafiltrationsretentat einer Diafiltration durch mindestens eine zweite Diafiltrations-/Ultrafiltrationsmembran ausgesetzt wird, wodurch ein zweites Diafiltrationspermeat und ein zweites Diafiltrationsretentat erzeugt werden; und wobei das zweite Diafiltrationspermeat durch die Nanofiltrationsmembran gefiltert wird.
  11. Verfahren nach Anspruch 6, wobei von dem ersten Ultrafiltrationsretentat, dem zweiten Ultrafiltrationsretentat und dem Nanofiltrationspermeat und einem Elektrodialysekonzentrat oder -rückstand mindestens zwei zur Herstellung von Melasse vereinigt werden.
  12. Verfahren nach Anspruch 10, wobei zumindest das erste Diafiltrationsretentat, das zweite Diafiltrationsretentat und das Nanofiltrationspermeat zur Herstellung von Melasse vereinigt werden.
  13. Verfahren nach Anspruch 6, das ferner das Eindampfen des Nanofiltrationsretentats zur Herstellung eines konzentrierten Sirups und das Auskristallisieren von Weißzucker aus dem konzentrieren Sirup aufweist.
  14. Verfahren nach Anspruch 7, wobei der gereinigte Saft eine Aschekonzentration von nicht mehr als 2,5 Gew.-% auf Trockenstoffbasis aufweist, und das ferner das Eindampfen des gereinigten Safts zur Herstellung eines konzentrierten Sirups und das Auskristallisieren von Weißzucker aus dem konzentrierten Sirup aufweist.
  15. Verfahren nach Anspruch 14, wobei das Verfahren zwei Kristallisationen von Weißzucker aus dem konzentrierten Sirup aufweist.
  16. Verfahren nach Anspruch 6, wobei der Saft während der Filtration durch die erste Ultrafiltrationsmembran eine Temperatur von 60 - 93°C (140 - 200°F) aufweist.
  17. Verfahren nach Anspruch 6, wobei die erste Ultrafiltrationsmembran eine Molekulargewichtsgrenze von mindestens 2000 Dalton und eine Porengröße von nicht mehr als 0,1 µm aufweist.
  18. Verfahren nach Anspruch 17, wobei die erste Ultrafiltrationsmembran eine Molekulargewichtsgrenze von 4000-200000 Dalton aufweist.
  19. Verfahren nach Anspruch 6, wobei das erste Ultrafiltrationspermeat eine Farbe von 3000 - 10000 icu und das zweite Ultrafiltrationspermeat eine Farbe von nicht mehr als 4000 icu aufweist.
  20. Verfahren nach Anspruch 6, wobei die zweite Ultrafiltrationsmembran eine Molekulargewichtsgrenze von 500 - 5000 Dalton aufweist.
  21. Verfahren nach Anspruch 20, wobei die zweite Ultrafiltrationsmembran eine Molekulargewichtsgrenze von 1000 - 4000 Dalton aufweist.
  22. Verfahren nach Anspruch 6, wobei das Nanofiltrationspermeat mindestens 30 Gew.-% auf Trockenstoffbasis der im Zulaufsaft vorhandenen Asche, mindestens 30 Gew.-% auf Trockenstoffbasis der im Zulaufsaft vorhandenen Invertzucker und mindestens 25 Gew.-% auf Trockenstoffbasis des im Zulaufsaft vorhandenen Betains aufweist.
  23. Verfahren nach Anspruch 6, wobei mindestens ein wäßriger Strom, ausgewählt aus der Gruppe, die aus dem Zulaufsaft, dem ersten Ultrafiltrationspermeat, dem zweiten Ultrafiltrationspermeat und dem Nanofiltrationsretentat besteht, in Kontakt mit einem Mittel gebracht wird, das aus der Gruppe ausgewählt ist, die aus Schwefeldioxid, Sulfitsalzen, Bisulfitsalzen, Metabisulfitsalzen, Dithionitsalzen und Gemischen daraus besteht, in einem Anteil, der ausreicht, um ein äquivalente Schwefeldioxidkonzentration von mindestens 100 ppm in dem Strom bereitzustellen.
  24. Verfahren nach einem der Ansprüche 1 bis 23, wobei kein Kalk und kein Kohlendioxid mit einem der Permeate in Kontakt gebracht werden.
  25. Verfahren nach Anspruch 6, das ferner den Schritt zum Einleiten einer ausreichenden Luftmenge in den Zulaufsaft aufweist, um eine Polymerisation von Farbkörpern vor der Filtration durch die erste Ultrafiltrationsmembran zu verursachen, wobei mindestens ein Teil der Farbkörper durch die Filtration in der ersten Ultrafiltrationsmembran aus dem Saft entfernt werden.
EP00957444A 1999-08-19 2000-08-15 Membranfiltrationsverfahren fur zuckerrüben Expired - Lifetime EP1204767B1 (de)

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US09/376,026 US6387186B1 (en) 1999-08-19 1999-08-19 Process for production of purified beet juice for sugar manufacture
US618416 2000-07-18
US618831 2000-07-18
US09/618,416 US6406547B1 (en) 2000-07-18 2000-07-18 Sugar beet membrane filtration process
US09/618,831 US6440222B1 (en) 2000-07-18 2000-07-18 Sugar beet membrane filtration process
PCT/US2000/022301 WO2001014594A2 (en) 1999-08-19 2000-08-15 Sugar beet membrane filtration process

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Families Citing this family (17)

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Publication number Priority date Publication date Assignee Title
ES2297041T3 (es) * 2001-08-24 2008-05-01 Danisco Sugar A/S Un procedimiento para la preparacion de azucar blanco y moreno a partir de remolacha azucarera.
WO2003089673A1 (en) * 2002-04-15 2003-10-30 Co2 Solutions, Llc A system to produce sugar from plant materials
FR2838751B1 (fr) * 2002-04-17 2007-03-09 Applexion Ste Nouvelle De Rech Procede et installation de fabrication de sucre raffine a partir de jus sucre
FI20021251A0 (fi) * 2002-06-26 2002-06-26 Finnfeeds Finland Oy Menetelmä betaiinin talteenottamiseksi
GB2408262B (en) * 2003-11-24 2007-09-12 British Sugar Plc A method of preparation of L-arabinose
GB2433518A (en) * 2005-12-21 2007-06-27 Danisco Process for the recovery of sucrose and non-sucrose materials
FI20065363A0 (fi) * 2006-05-30 2006-05-30 Danisco Sweeteners Oy Erotusmenetelmä
FR2928817B1 (fr) 2008-03-19 2010-12-17 Ecopsi Procede et unite de production de dreches de betteraves et de jus sucre a partir de betteraves
MX339772B (es) * 2010-08-13 2016-06-09 Rdm Empreendimentos E Participações S A * Metodo y composicion para producir azucar clarificada.
UA112671C2 (uk) 2011-12-23 2016-10-10 Нестек С.А. Спосіб одержання смако-ароматичної композиції зі смаком і ароматом умамі
US9487840B2 (en) * 2013-09-16 2016-11-08 Api Intellectual Property Holdings, Llc Processes and apparatus for refining sugarcane to produce sugars, biofuels, and/or biochemicals
CN105154591B (zh) * 2015-08-13 2018-11-20 开远滇蔗园科技有限公司 一种甘蔗原汁红糖粉的生产方法
RU2619309C2 (ru) * 2015-10-19 2017-05-15 Федеральное государственное бюджетное образовательное учреждение высшего образования "Московский государственный университет технологий и управления имени К.Г. Разумовского (Первый казачий университет" (ФГБОУ ВО "МГУТУ им. К.Г. Разумовского (ПКУ)") Способ производства кристаллического сахара
CN111269181B (zh) * 2019-12-31 2023-09-19 江苏久吾高科技股份有限公司 一种盐酸青藤碱的提纯方法及装置
CA3190261A1 (en) * 2020-07-31 2022-04-21 Hydrite Chemical Co. Method for controlling microbial growth in sugar processing
KR20230084565A (ko) * 2020-11-30 2023-06-13 신히가시니혼 세이토 가부시키가이샤 원료당 및 정제당의 제조 프로세스
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Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB477312A (en) * 1935-05-07 1937-12-23 Jose Antich Improvements in or relating to the treatment of carob beans (ceratonia siliqua l) and similar plants
GB1361674A (en) * 1971-04-23 1974-07-30 Danske Sukkerfab Process for the purification and clarification of sugar juices
GB1428790A (en) * 1973-09-28 1976-03-17 Tate & Lyle Ltd Production of cane sugar
US4057437A (en) * 1976-06-09 1977-11-08 Sparkler Mfg. Co. Continuous belt filter and filtration method
SE441932B (sv) * 1981-01-14 1985-11-18 Danske Sukkerfab Forfarande for rening av sockersaft framstelld genom extraktion av sockerbetssnitsel
NL8301786A (nl) * 1983-05-19 1984-12-17 Suiker Unie Werkwijze voor het winnen van disacchariden uit disacchariden bevattende knolgewassen, onder toepassing van een extractie met onverwarmd water.
AU635352B2 (en) * 1990-11-09 1993-03-18 Applied Membrane Systems Pty Ltd A method and apparatus for fractionation of sugar containing solution
US5281279A (en) * 1991-11-04 1994-01-25 Gil Enrique G Process for producing refined sugar from raw juices
US5554227A (en) * 1993-11-12 1996-09-10 Societe Nouvelle De Recherches Et D'applications Industrielles D'echangeurs D'ions Applexion Process of manufacturing crystal sugar from an aqueous sugar juice such as cane juice or sugar beet juice
US5468300A (en) * 1994-04-07 1995-11-21 International Food Processing Incorporated Process for producing refined sugar directly from sugarcane
BR9508477A (pt) * 1994-08-03 1997-10-28 Int Food Processing Inc Processo para a produção de açúcar refinado
US5759283A (en) * 1996-05-14 1998-06-02 The Western Sugar Company Method for processing sugar beets to produce a purified beet juice product

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EP1788100A2 (de) 2007-05-23
WO2001014594A2 (en) 2001-03-01
PL353772A1 (en) 2003-12-01
AU6906300A (en) 2001-03-19
EP1204767A2 (de) 2002-05-15
DE60034127T2 (de) 2007-12-06
EP1788099A2 (de) 2007-05-23
WO2001014594A3 (en) 2001-12-06
HUP0204353A2 (en) 2003-05-28
CZ2002570A3 (cs) 2002-11-13
SK3772002A3 (en) 2002-11-06
DE60034127D1 (de) 2007-05-10
HUP0204353A3 (en) 2004-12-28
ATE358187T1 (de) 2007-04-15

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