AU683738B2 - Regeneration of pulp liquors - Google Patents
Regeneration of pulp liquorsInfo
- Publication number
- AU683738B2 AU683738B2 AU20615/95A AU2061595A AU683738B2 AU 683738 B2 AU683738 B2 AU 683738B2 AU 20615/95 A AU20615/95 A AU 20615/95A AU 2061595 A AU2061595 A AU 2061595A AU 683738 B2 AU683738 B2 AU 683738B2
- Authority
- AU
- Australia
- Prior art keywords
- paper
- treatment
- spent
- liquid phase
- liquors
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 230000008929 regeneration Effects 0.000 title description 2
- 238000011069 regeneration method Methods 0.000 title description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 60
- 238000011282 treatment Methods 0.000 claims description 48
- 238000000034 method Methods 0.000 claims description 41
- 239000010802 sludge Substances 0.000 claims description 29
- 239000007787 solid Substances 0.000 claims description 28
- 239000007788 liquid Substances 0.000 claims description 21
- 239000007791 liquid phase Substances 0.000 claims description 18
- 238000001223 reverse osmosis Methods 0.000 claims description 18
- 239000010893 paper waste Substances 0.000 claims description 14
- 238000001914 filtration Methods 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 239000002910 solid waste Substances 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- 230000008020 evaporation Effects 0.000 claims description 5
- 239000011368 organic material Substances 0.000 claims description 5
- 239000000243 solution Substances 0.000 claims description 5
- 238000001471 micro-filtration Methods 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 4
- 239000012141 concentrate Substances 0.000 claims description 3
- 239000012266 salt solution Substances 0.000 claims description 2
- 239000000123 paper Substances 0.000 description 44
- 230000008569 process Effects 0.000 description 35
- 238000009300 dissolved air flotation Methods 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 238000004537 pulping Methods 0.000 description 12
- 239000000126 substance Substances 0.000 description 10
- 239000011087 paperboard Substances 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000002699 waste material Substances 0.000 description 7
- 241000894006 Bacteria Species 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- -1 aliphatic fatty acids Chemical class 0.000 description 5
- 210000000038 chest Anatomy 0.000 description 5
- 238000011109 contamination Methods 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000004513 sizing Methods 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- 238000004065 wastewater treatment Methods 0.000 description 4
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000013505 freshwater Substances 0.000 description 3
- 239000012466 permeate Substances 0.000 description 3
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000003643 water by type Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000001164 aluminium sulphate Substances 0.000 description 2
- 235000011128 aluminium sulphate Nutrition 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 238000011001 backwashing Methods 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000010791 domestic waste Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000010899 old newspaper Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000012905 visible particle Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/64—Paper recycling
Landscapes
- Paper (AREA)
Description
REGENERATION OF PULP LIQUORS
This invention relates to the manufacture of paper and paperboard and in particular, from recycled paper or paperboard materials.
Conventional paper mill systems are run so that process waters are recycled many times during the production of paper and paperboard. Eventually, however, the concentrations of dissolved inorganic salts and organic materials in the process waters build up to a level where further recycling is impractical without having an adverse effect on the quality of the paper produced. These impurities generally have a high BOD (biological oxygen demand) and a high COD (chemical oxygen demand). Additionally, the dissolved materials promote unacceptable levels of corrosion in process equipment and growth of bacterial slimes, leading to blockage of pipes and sprays. These restrictions necessitate the discharge of large volumes of waste water into conventional waste water treatment plants, located either on the site of the mill itself, or at some remote site, which is often a municipal sewage treatment plant. To make up for this discharge paper mills must also take in large volumes of fresh water for process use. Consequently, paper making which utilises conventional waste water treatment techniques places a heavy demand on often scarce fresh water resources and also on the waste water treatment systems themselves.
The process of papermaking (whether from virgin pulp or wastepaper) involves diluting refined cellulose fibres with massive quantities of water, forming the fibres into a sheet in the forming section of a paper machine, then progressively removing the water until the result is a dry sheet of paper. Vegetable starches are frequently added to the suspension of fibres or to the sheet at an intermediate stage in the drying process to increase the strength of the paper or to reduce the rate at which the paper absorbs water.
In addition to the starch, chemicals are employed in ancillary treatments i.e. acids and caustic soda for water pH control, and flocculants and retention aids to improve the retention of the cellulose fibres and other components in the papermaking process. In many cases the water soluble chemical sodium
sulphate is generated as a by-product of the use of aluminium sulphate in the sizing process.
Since not all the cellulose fibre or chemicals are retained in the sheet of paper, the water becomes contaminated by this non-retained material, and eventually reaches a level of contamination where it has to be rejected from the system as effluent.
The nature of this contamination can be categorised into the following forms:
1. Suspended solids (visible particles) both organic and inorganic 2. Dissolved solids (again, organic and inorganic, but in the main dissolved mineral salts) 3. Bacteria
A proportion of both forms of solids (BOD - Biological oxygen demand and COD - Chemical oxygen demand) require oxidation to convert them to inert and harmless substances.
Paper and paperboard mills in the USA in the period from 1956 to 1966 typically discharged between 3800 and 53000 litres of water per ton of production, the average for the industry being 17680 litres per ton. In 1982 the United States Environmental Protection Authority (EPA) developed guidelines which outlined industry targets to be between 1130 to 41300 litres per ton, the industry average being 17400.
Since the introduction of the EPA development document, 1988/89 industry operations have reduced water discharges to between 530 to 27820 litres per ton with the current average usage being 9530. Whilst a typical paper mill recycles process water many times in the production of paper and paperboard, eventually the water reaches a level of contamination which precludes its further use and at this stage, the process water, often termed excess water, is discharged from the mill as effluent.
Historically the EPA has regulated these discharges, particularly in terms of BOD5 (Five Day Biological Oxygen Demand) and TSS (Total Suspended Solids) as outlined below.
Raw Effluent Characteristics
Historical EPA 1988-89 1956-66 Development Operations 1981
BOD5 lbs per ton 10.2 to 99 1.9 to 135 8.8 to 39.7
(average) 29.4 18.4 22.7
TSS lbs per ton 4.5 to 101 0.9 to 95.3 1.7 to 44.5
(average) 36.5 20.8 15.7
Attempts at purifying effluents have been made as exemplified in USA patent 2897148. There has been at least one attempt to design a paper mill having zero liquid discharge but this was in a mill converting wood chips into paper pulp. The complexity of the composition of effluents in a recycled paper mill is much greater because of the presence of inks, sizing agents and other chemicals in the paper to be recycled. It is an object of this invention to provide a process and a paper mill for making paper which involves treating paper mill process water that would normally be liquid effluent discharge, removing the contamination and then returning the water to the mill in "fresh" condition, such that there is no liquid effluent. To this end the present invention provides a method of producing paper from waste paper with the production of no liquid effluent which includes the steps of treating the waste paper with aqueous treatment liquors, recovering converted paper and spent treatment liquors, characterized in that the spent treatment liquors are subsequently: subjected to an oxidative treatment which produces a sludge; separating the liquid phase from the sludge; subjecting the separated liquid phase to reverse osmosis treatment; and reusing all of the treated liquid phase to form fresh aqueous treatment liquor. It is preferred that the separated liquid phase is subjected to microfiltration prior to reverse osmosis treatment. In a preferred embodiment the invention provides a method which includes the steps of:
removing suspended solids from spent treatment liquors; optionally treating the spent treatment liquors in a clarifier; passing the spent treatment liquors to a cyclic activated sludge reaction system for oxidative treatment which produces a sludge; separating the liquid phase from the sludge; subjecting the separated liquid phase to a continuous microfilter to remove suspended particles; subjecting the microfiltered water to reverse osmosis treatment to concentrate dissolved solids and produce a treated liquid phase and a concentrated salt solution; and crystallizing the dissolved salts in an evaporation unit to produce a solid waste.
It is preferred that the filtration unit for removing suspended solids from spent treatment liquors comprises a series of filtration means such as disk type filtration means, flotation type filtration means and/or sand type filtration means.
Preferably the spent treatment liquours are subjected to a clarifier prior to oxidation of the organic materials.
This invention is partly predicated on the discovery that it is advantageous to remove a substantial portion of the organic contaminants prior to and separately from the removal of the inorganic contaminants.
Oxidation of inorganic materials may also occur in the biological treatment unit however, most of these oxidised materials remain in solution, in contrast to the majority of the oxidised organic materials which are removed in a separable sludge. This invention also provides a paper mill for producing paper from waste paper in which no liquid effluent is produced which includes the steps of treating the waste paper with aqueous treatment liquors and recovering converted paper and spent treatment liquors comprising: a biological treatment unit to oxidize a substantial portion of the organic materials in the spent aqueous treatment liquors to produce a separable sludge;
and a reverse osmosis unit to produce a concentrated solution of salts and a treated liquid phase.
The paper mill preferably also includes a filtration unit suitable for filtering the spent aqueous treatment liquors prior to subjecting the spent aqueous treatment liquors to oxidation, a microfiltration unit to remove any undissolved matter remaining in the liquid phase following biological treatment and an evaporation unit suitable to produce a solid waste product from the concentrated solution of salts. Some treatments of spent liquors include combustion of the liquid at high temperatures to burn the organic components of the waste waters. However, where the waste waters include sizing agents and sizing agent byproducts such as sodium sulphate, combustion can give rise to unacceptable flue gases such as sulphides or oxides of sulphur. Thus this invention also avoids producing any unacceptable gaseous as well as liquid effluent and avoids the use of an expensive boiler for combustion.
One embodiment of the present invention will now be described with reference to the schematic flow diagram of a paper mill as shown in Figure 1. Figures 2, 3A and 3B (Figures 3A and 3B each show one half of a schematic flow diagram) show a flow diagram of the spent liquor treatment process.
In this plant no liquid streams are discharged.
The main mill process area comprises three main process systems. The first process system is for pulping of waste paper such as mixed domestic waste paper, old corrugated containers (OCC), container makers' (box makers') clippings, or a variety of white waste papers such as mixed office waste, printers waste and old newspapers and old magazines which generates a suspension of fibres in water, called "stock", which must be subjected to further processing to remove contaminants and to improve the bonding properties of the fibres, in order to ensure that paperboard with adequate appearance and strength properties can be manufactured.
The waste papers are generally reslushed in one of the dirtier recovered mill process water streams in a vessel known as a hydropulper. Temperature
and mechanical agitation are generally sufficient to separate the bulk of the fibres. In some cases, for example in reslushing paperboards containing resins and other additives to enhance wet strength, sodium hydroxide may be added to break down the additives. Dispersants may also be added to disperse waxes and hot melt glues in a later dispersing step. When white waste papers are the raw material, sodium hydroxide, hydrogen peroxide and sodium silicate may also be added to the pulp in the hydropulper, particularly if de-inking is to be carried out at a later stage. In this case surfactant de-inking chemicals and calcium salts of long chain aliphatic fatty acids are usually added as well, the latter to collect the ink particles being liberated by the mechanical action. If de- inking is carried out, additional brightening stages, using sodium hydroxide and hydrogen peroxide (with silicates or chelants), formamidine sulphinic acid and/or sodium dithionite are frequently incorporated.
The second major process system for cleaning and refining the stock is called stock preparation. In the case of white waste papers, a de-inking plant may be included in the stock cleaning process. Stock preparation involves passage of the stock through a series of slotted, or hole pressure screens to remove from the stock particles which are larger than individual fibres; then through a series of high density (HD) and medium density (MD) liquid cyclones, which remove sequentially high specific gravity contaminants and low specific gravity contaminants from the stock; and then optionally through dispersers to reduce the particle size of any remaining waxes and glues; then through refiners which apply kinetic energy to the fibres in order to develop bonding characteristics, and finally into one or more chests for storage prior to use on the paper machine. At many intermediate stages during stock preparation, dilution or dewatering of the stock can occur in order to adjust the concentration of fibres per unit volume of water (the "consistency" of the stock) to a level which ensures either maximum efficiency of contaminant removal, or efficient transport to the next processing stage. The third major process to which the stock is subjected is papermaking on a paper machine, where the stock is filtered through one or more moving woven fabrics, called "wires", to form a continuous single or multiple ply web of fibres,
which is dried to form paper or paperboard. The paper pulp going forward to the paper machine is usually mixed with either rosin size (which may be partially catonised) and aluminium sulphate, or with synthetic sizes, such as alkyl ketene dimer (AKD), or alkenyl succinic anhydride (ASA), neither of which require aluminium ions for their sizing action. Other chemicals which may be added include cationic or amphoteric starches to enhance strength properties, various retention aids, cationic polymers which assist retention of mineral fillers and organic fines in the paper sheet, drainage aids (cationic polymers which facilitate the speed with which water can be removed from the sheet) and defoamers to prevent foam formation on the forming table of the machine or in the backwater chest under the machine.
Solid waste streams removed from the recycled fibre pulping system, and the stock preparation system are transferred to thickening devices and then to containers and are then transported directly to landfill disposal. All other waste streams are processed in the effluent treatment system, with resultant solid waste from the sludge belt press transported to landfill disposal and with cleaned and clarified water returned for re-use in the pulping and papermaking processes.
Two effluent streams flow from the main mill process areas to the effluent treatment system. One stream is pumped from the rejects tank in the recycled fibre pulping area. The second effluent stream is pumped from the mill U-drain system sump. A summary of the sources of individual effluents associated with reject streams in the OCC pulping and the stock preparation areas and from parts of the wet end of the paper machine is given in Tables 1A and 1 B.
TABLE 1A TYPICAL REJECTS HANDLED VIA
RECYCLE PULPING REJECTS TANK
Rejects Source Normal Flow oven dried tons per day / % fibre in water / litres per minute Pressure screens and MD liquid cyclones in stock preparation area 8.307 1.17 / 446.7
TABLE 1B
TYPICAL REJECTS HANDLED VIA U-DRAIN SUMP
Rejects Source Normal Flow oven dried tons per day / % fibre in water / litres per minute Paper Machine Drum Screen for Reject Removal 0.30 / 5.00 / 03.8
MD Liquid Cyclones in Stock Preparation Area 3.70/ 0.82/ 283.9
Fresh Water Strainer 0 /0/0
Strainer for High Pressure
Showers on Paper Machine 0 / 0 / 22.7
Uhle Box Filter 0 / 0 / 60.6 Dilution Chest Overflow 0 /0/0
The effluent flow into the Recycled Fibre Rejects Tank is normally 8/1/454 oven dried tons per day / percent fibre in water / litres per minute (ODTPD/consistency/lpm), but the flow can vary over a very wide range, depending on the design capacity of the pulping, stock preparation and paper making equipment. The effluent flow into the U-Drain Sump is normally 4/1/370 ODTPD/consistency/lpm), but this can also vary over a very wide range, depending on the design capacity of the pulping, stock preparation and paper making equipment.
The two effluent streams from the mill are pumped to an effluent feed tank via two lines, one from the cleaner rejects tank and one from the U-drain sumps (see Figure 3A). The effluent feed tank is equipped with an agitator and a level control system. The U-drain system provides surge volume capacity and is an integral part of the overall effluent feed flow and level control.
The U-drain sump is equipped with five lift pumps, with a total capacity of 1500 Ipm (litres per minute), to transfer material to the effluent feed tank. These pumps can be operated automatically by level control or by manual control. A recirculation line from the lift pump discharge header continuously flushes the suction areas of the three lift pumps to prevent plugging of pump suctions.
Material from an effluent system backwash surge tank is pumped to the effluent feed tank to return the stream to the effluent treatment system for solids separation and water reclaim. Discostrainer Material from the effluent feed tank is transferred to a discostrainer (a rotating fabric disk screen) for initial separation of suspended solids. The discharge pump from the effluent feed tank is equipped with a variable frequency drive for control of feed rate to the discostrainer. Flow rate from the effluent feed tank to the discostrainer is modulated based on liquid level in the effluent feed tank. Because discostrainer operating stability is sensitive to variations in feed rate, the rate of change of feed rate to the discostrainer is restrained to about 190 Ipm per minute.
As a means to achieve desired discostrainer rejects consistency, a remotely operated by-pass is provided to allow a portion of the feed to the discostrainer to be routed directly to the rejects outlet. After initial set-up, the by¬ pass does not require frequent adjustment. Beit Press
Rejects from the discostrainer flow by gravity to a belt press feed box where this stream is combined with other belt press feed streams. Provisions are included to allow addition of chemical additives to the discostrainer rejects stream enroute from the discostrainer to the belt press feed box. Reclaimed water tank
Accepts from the discostrainer flow by gravity to a reclaimed water tank. The reclaimed water tank may also receive the filtrate stream from the belt press, or this stream can be fed back to the effluent feed tank. The combined flow from the reclaimed water tank may be pumped, a mt a controlled rate to maintain tank level, as feed to a dissolved air flotation (DAF) clarifier. The discharge pump from the reclaimed water tank employs a variable frequency drive for flow rate control. DAF Clarifier
Commencement of suspended solids separation from the process stream is by a DAF clarifier. A recirculation pump transfers liquid from the DAF clarifier
vessel to an air dissolving tube where air is entrained in the stream, and the air- rich stream is returned to the DAF vessel.
Lightweight suspended solids float to the top of the DAF clarifier where they are skimmed off and transferred to a sludge rejects chamber for discharge. This material is discharged by gravity to a DAF sludge sump. Heavyweight suspended solids sink to the bottom of the DAF clarifier and are periodically purged to the DAF sludge sump. Material from the DAF sludge sump is pumped, at a controlled rate to maintain level in the sludge sump, to the belt press feed box. The discharge pump from the DAF sludge sump employs a variable frequency drive for flow rate control.
The accepts stream from the DAF clarifier is transferred by gravity to a DAF clear sump. The liquid is pumped, at a controlled rate to maintain sump level, from the DAF clear sump to a filtered water tank. The discharge pump from the DAF clear sump employs a variable frequency drive for flow rate control. Filtered Water Tank
A low pressure shower pump transfers a constant flow portion of the water from the filtered water tank to the discostrainer for process showers. A high pressure shower pump transfers a constant flow portion of the water from the filtered water tank to the belt press for process showers. The balance of the water from the filtered water tank is pumped, at a controlled rate to maintain tank level, to the Dynasand® filter header. The discharge pump from the filtered water tank to the Dynasand® filter header employs a variable frequency drive for flow rate control. Dvnasand® Filter The Dynasand® filter is a continuous backwash, upflow, deep-bed granular media filter (available from Parkson Corporation, Fort Lauderdale, Florida).
Flow in the Dynasand® filter header is normally split to feed the combination of the Dynasand® filter and the sequential batch reactor (SBR) system. However, to provide flexibility to optimize the overall process and to
accommodate equipment maintenance without mill production loss, the system is configured to allow:
All of the flow to by-pass the Dynasand® filter and go directly to the SBR system, or All of the flow to flow in series to the Dynasand® filter and then to the SBR system, or
All of the flow to be processed through the Dynasand® filter with by-pass of the SBR system and all processes down-stream of the SBR system, or
All of the flow to by-pass the Dynasand® filter and the SBR system, with all flow recirculated directly from the Dynasand® filter header to the combined white water chest for reuse in the recycle pulping and papermaking processes. Under normal operating conditions, the flow from the Dynasand® filter header is split to maintain a minimum feed rate of 190 Ipm to the Dynasand® filter, with the balance of the flow, up to a maximum of 1325 Ipm, going to the SBR (sequential batch reactor) system for BOD5 reduction. When the total flow rate in the Dynasand® filter header is greater than 1515 Ipm, feed rate to the SBR system is controlled at 1325 Ipm, with the balance of the flow going to the Dynasand® filter; when the total flow rate in the Dynasand® filter header is less than 1515 Ipm, feed rate to the Dynasand® filter is maintained at 190 Ipm, with the balance of the flow going to the SBR. There is also a provision for the feed to the Dynasand® filter to by-pass the filter directly to the Dynasand® filtered water standpipe for the return to the contaminated white water tank. SBR System (Cyclic Activated Sludαe System)
The SBR system consists of two batch reaction vessels which are operated sequentially to effect BOD5 and COD reduction using mixed cultures of aerobic micro-organisms. The two reaction vessels are sequentially filled with effluent, which has a BOD5 concentration typically in the range 500 to 2500 mg/L and a total suspended solids (TSS) concentration in the range 60 to 800 mg/L, from the Dynasand® filter header, and/or from the Dynasand® filter, and are held
for batch reaction for a period of 8 to 16 hours at pH 7 to 8 at a temperature between 65-100°F in the presence of a mixed culture of aerobic non-filamentous microorganisms.
Special strains of bacteria are not used to inoculate the cyclic activated sludge system. In the process of reslushing the waste paper, a naturally occurring population of bacteria on the waste paper will be mixed with mill process waters also containing mixed bacteria from the air and from earlier batches of waste paper. These populations feed on the starch which is washed off the waste paper and a portion of them will be carried forward into the waste water treatment plant where conditions in the cyclic activated sludge system will encourage growth with concomitant BOD and COD removal. Bacteria and other slime-producing organisms are ubiquitous components of paper machine backwater systems. Excessive growth can cause odours, spray and pipe blockages and ultimately contamination of the paper sheet itself. For this reason, bacteriocides and slimicides are usually added to keep bacterial and slime levels to manageable levels.
During the reaction phase of the process, which lasts from 6 to 14 hours, high volume centrifugal blowers force air upward through the quiescent volume to effect oxidation. The concentration of dissolved oxygen in the waste water in
< the reaction vessel is maintained in the optimum range of 1 to 2 mg/l by means of a variable frequency drive on at least one of the air blowers under the control of a dissolved oxygen sensor. At the completion of the reaction period the passage of air is discontinued and the resulting bio-sludge is allowed to settle for a period of 1 to 2 hours under anaerobic conditions. The upper portion of the reaction volume is then decanted to the SBR decant surge tank. The bio-sludge formed during the reaction settles to the bottom of the reaction vessel and is pumped to the SBR sludge surge tank.
Sludge from the SBR sludge surge tank after optional further oxidation or lime stabilization is pumped to the belt press for dewatering. The pump from the SBR sludge surge tank employs a variable frequency drive to maintain flow rate based on tank level.
Decanted liquid from the SBR decant surge tank which is found to have a
BOD5 concentration in the range of 0 to 70 mg/l and a TSS concentration in the range 5 to 600 mg/l is continuously pumped via filters to the CMF (continuous microfilter) feed tank. The pump from the SBR decant surge tank employs a variable frequency drive to maintain flow rate based on tank level.
Under operating conditions in the SBR, some non-settling, filamentous bacterial populations can sometimes increase to a point where the TSS concentrations of the decanted liquid rise above 1000 mg/l, at which point the downstream continuous microfilter requires backwashing at an unacceptably high frequency. Under these conditions, the dissolved air filtration clarifier can be used temporarily to clarify the decanted water from the SBR. The dissolved air flotation clarifier is ideal for removing solid contaminants, which do not float and which do not settle, until control has been regained over the microbiological populations in the SBR and the liquid can be provided as a clear feed, with a TSS concentration below 600 mg/l to the CMF.
The CMF feed tank may be modified so that the lower portion of the tank can act as a stagnant zone to allow settling of the bulk of the precipitated material in order to minimize the separation load on the downstream CMF unit.
Enroute from the SBR decant surge tank to the CMF feed tank, a coarse strainer is employed to remove large entrained suspended particles. Continuous backwash from the coarse strainer is discharged to the backwash surge tank.
In order to precipitate metal-organic complexes in the liquid coming from the SBR decant surge tank, which will precipitate in the downstream reverse osmosis stage and damage the membranes, it is preferred that the pH of the liquid coming from the SBR decant surge tank be reduced to below 6.0 by the addition of hydrochloric acid or sulphuric acid under automatic pH control.
Provisions are included to allow the stream from the CMF feed tank to be temporarily diverted to the combined white water chest for complete closed-loop recirculation. This provision is included to allow short-term outages for maintenance of the downstream CMF unit, RO system, and crystallizer without stopping mill production processes.
Continuous Microfilter
The continuous microfilter unit (CMF) removes minute suspended particles and bacteria entrained in the feed stream and the precipitated metal- organic complexes from the previous pH adjustment stage. The CMF unit employs relatively high pressure drop across a polypropylene filtration membrane which is formed with bundles of hollow fibres, to accomplish the filtering process (available from Memtec America Corporation, Maryland). The filtration membrane preferably has a pore size of about 0.2 micron although it can range from 0.1 micron up to 0.5 micron. Backwash from the CMF unit is discharged to the CMF backwash tank, from which the material is continuously pumped to the backwash surge tank at a controlled rate to maintain level in the CMF backwash tank. The discharge pump from the CMF backwash tank employs a variable frequency drive for flow control.
The clean filtrate from the CMF unit, which has a TSS concentration in the range 0 to 3 mg/l, is discharged to the microfiltered (MF) water tank. From the MF water tank, the flow is split, with a constant flow portion of about 490 Ipm of the highly filtered water treated for removal of dissolved solids and with the balance of between 150 and 300 Ipm of the stream returned to the mill water tank for reuse in the recycle pulping and papermaking process. The discharge pump from the MF water tank to the mill water tank employs a variable frequency drive for flow control. The flow rate is controlled to maintain level in the MF water tank.
The portion of the highly filtered water that is treated for removal of dissolved solids is pumped from the MF water tank to the reverse osmosis (RO) feed tank for further processing. If desired, an activated carbon filter unit may be included between the MF water tank and the RO feed tank to allow for further reduction of high molecular weight COD species which have not been adequately removed by the SBR system. Reverse Osmosis A reverse osmosis system is used to concentrate dissolved solids for subsequent removal. Typical total dissolved solids (TDS) concentrations in the
RO feed tank are in the range of 500 to 5000 mg/l. The RO system includes fully redundant processing units to assure continuity of operation.
In the RO system, a relatively high pressure drop of about 37 bar across a semi-permeable separation membrane is used to produce a stream with high dissolved solids concentration and a stream that is virtually free of dissolved solids. The clean stream from the RO system is discharged to the permeate tank and from there to the mill water tank for reuse in the recycle pulping and papermaking process. The discharge pump from the permeate tank to the mill water tank employs a variable frequency drive to achieve flow control required to maintain level in the permeate tank. The stream with concentrated dissolved solids (brine) is discharged to the crystallizer system for removal of the dissolved solids. Crystallizer
A crystallizer system is used for removal of dissolved solids from the feed stream. The crystallizer system employs a combination of heat and vacuum to evaporate the water from the feed stream, creating molten solids for disposal and water vapour for reclaim.
Molten solids from the crystallizer system are discharged as sludge for landfill disposal. On cooling below approximately 120°F, the discharged material forms rόck-like solids for disposal.
Water vapour created in the evaporation process of the crystallizer system is condensed. The condensate is transferred to the mill water tank for reuse in the recycle pulping and papermaking processes.
Claims (7)
1. A method of producing paper from waste paper with the production of no liquid effluent which includes the steps of treating the waste paper with aqueous treatment liquors, recovering converted paper and spent treatment liquors, characterized in that the spent treatment liquors are subsequently: subjected to an oxidative treatment which produces a sludge; separating the liquid phase from the sludge; subjecting the separated liquid phase to reverse osmosis treatment; and reusing all of the treated liquid phase to form fresh aqueous treatment liquor.
2. A method as claimed in claim 1 wherein the separated liquid phase is subjected to microfiltration prior to reverse osmosis treatment.
3. A method as claimed in claim 1 or claim 2 which includes the steps of: removing suspended solids from spent treatment liquors; optionally treating the spent treatment liquors in a clarifier; passing the spent treatment liquors to a cyclic activated sludge reaction system for oxidative treatment which produces a sludge; separating the liquid phase from the sludge; subjecting the separated liquid phase to a continuous microfilter to remove suspended particles; subjecting the microfiltered water to reverse osmosis treatment to concentrate dissolved solids and produce a treated liquid phase and a concentrated salt solution; and crystallizing the dissolved salts in an evaporation unit to produce a solid waste.
4. A paper mill for producing paper from waste paper in which no liquid effluent is produced which includes the steps of treating the waste paper with aqueous treatment liquors and recovering converted paper and spent treatment liquors comprising: a biological treatment unit to oxidize a substantial portion of the organic materials in the spent aqueous treatment liquors to produce a separable sludge; and a reverse osmosis unit to produce a concentrated solution of salts and a treated liquid phase.
5. A paper mill as claimed in claim 4 also comprising: a filtration unit suitable for filtering the spent aqueous treatment liquors prior to subjecting the spent aqueous treatment liquors to oxidation.
6. A paper mill as claimed in claim 4 or claim 5 also comprising: a microfiltration unit to remove any undissolved matter remaining in the liquid phase exiting the biological treatment unit.
7. A paper mill as claimed in any one of claims 4 to 6 also comprising: an evaporation unit suitable to produce a solid waste product from the concentrated solution of salts.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU20615/95A AU683738B2 (en) | 1994-03-17 | 1995-03-17 | Regeneration of pulp liquors |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPM4527 | 1994-03-17 | ||
| AUPM4527A AUPM452794A0 (en) | 1994-03-17 | 1994-03-17 | Waste water recovery system |
| PCT/AU1995/000150 WO1995025197A1 (en) | 1994-03-17 | 1995-03-17 | Regeneration of pulp liquors |
| AU20615/95A AU683738B2 (en) | 1994-03-17 | 1995-03-17 | Regeneration of pulp liquors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2061595A AU2061595A (en) | 1995-10-03 |
| AU683738B2 true AU683738B2 (en) | 1997-11-20 |
Family
ID=25617939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU20615/95A Ceased AU683738B2 (en) | 1994-03-17 | 1995-03-17 | Regeneration of pulp liquors |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU683738B2 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3873414A (en) * | 1971-10-25 | 1975-03-25 | Air Liquide | Process for the treatment of black liquor of cellulosic pulp wherein oxidation is performed both before and after black liquor concentration |
| US4155845A (en) * | 1976-05-12 | 1979-05-22 | Rhone-Poulenc Industries | Treatment of pulp mill effluents |
| AU6125380A (en) * | 1979-05-18 | 1980-12-03 | Australian Paper Manufacturers Limited | Pulping liquor reutilization |
-
1995
- 1995-03-17 AU AU20615/95A patent/AU683738B2/en not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3873414A (en) * | 1971-10-25 | 1975-03-25 | Air Liquide | Process for the treatment of black liquor of cellulosic pulp wherein oxidation is performed both before and after black liquor concentration |
| US4155845A (en) * | 1976-05-12 | 1979-05-22 | Rhone-Poulenc Industries | Treatment of pulp mill effluents |
| AU6125380A (en) * | 1979-05-18 | 1980-12-03 | Australian Paper Manufacturers Limited | Pulping liquor reutilization |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2061595A (en) | 1995-10-03 |
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Owner name: PAPER AUSTRALIA PTY LTD Free format text: FORMER OWNER WAS: AMCOR LIMITED |
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| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |