EP1058713A1 - Lignin based colloidal compositions - Google Patents
Lignin based colloidal compositionsInfo
- Publication number
- EP1058713A1 EP1058713A1 EP99906000A EP99906000A EP1058713A1 EP 1058713 A1 EP1058713 A1 EP 1058713A1 EP 99906000 A EP99906000 A EP 99906000A EP 99906000 A EP99906000 A EP 99906000A EP 1058713 A1 EP1058713 A1 EP 1058713A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bitumen
- lignin
- spent
- pulping liquor
- colloidal dispersion
- 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.)
- Withdrawn
Links
- 229920005610 lignin Polymers 0.000 title claims abstract description 35
- 239000000203 mixture Substances 0.000 title claims description 45
- 239000010426 asphalt Substances 0.000 claims abstract description 97
- 238000000034 method Methods 0.000 claims abstract description 47
- 239000010687 lubricating oil Substances 0.000 claims abstract description 28
- 238000001246 colloidal dispersion Methods 0.000 claims abstract description 24
- 239000002253 acid Substances 0.000 claims abstract description 19
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 16
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 13
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 239000006185 dispersion Substances 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000002655 kraft paper Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 6
- 239000003945 anionic surfactant Substances 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- 238000010306 acid treatment Methods 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 238000005187 foaming Methods 0.000 claims description 2
- 239000003265 pulping liquor Substances 0.000 claims 20
- 238000002156 mixing Methods 0.000 claims 4
- 125000005313 fatty acid group Chemical group 0.000 claims 1
- CXPOFJRHCFPDRI-UHFFFAOYSA-N dodecylbenzene;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1 CXPOFJRHCFPDRI-UHFFFAOYSA-N 0.000 abstract description 16
- 238000013019 agitation Methods 0.000 abstract description 5
- 239000000084 colloidal system Substances 0.000 abstract description 5
- -1 sulfuric acid Chemical class 0.000 abstract description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 238000003756 stirring Methods 0.000 description 7
- 239000002023 wood Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 238000004537 pulping Methods 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000010705 motor oil Substances 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000004533 oil dispersion Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002025 wood fiber Substances 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- NGWKGSCSHDHHAJ-YPFQVHCOSA-N Liquoric acid Chemical compound C1C[C@H](O)C(C)(C)C2CC[C@@]3(C)[C@]4(C)C[C@H]5O[C@@H]([C@](C6)(C)C(O)=O)C[C@@]5(C)[C@@H]6C4=CC(=O)C3[C@]21C NGWKGSCSHDHHAJ-YPFQVHCOSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910052806 inorganic carbonate Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052945 inorganic sulfide Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229940023462 paste product Drugs 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007962 solid dispersion Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/005—Lignin
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C11/00—Regeneration of pulp liquors or effluent waste waters
- D21C11/0007—Recovery of by-products, i.e. compounds other than those necessary for pulping, for multiple uses or not otherwise provided for
Definitions
- the present invention relates to the processing of black liquor and the preparation of bitumen compositions containing black liquor.
- Black liquor is an aqueous alkaline pulping residue produced in Kraft pulping of wood chips in a pulp mill to provide wood fibers for paper-making.
- Black liquor generally contains about 55 to 65% solids comprising lignin, sodium salts of poly-saccharinic acids, organic and inorganic sulfides and carbonates and many other compounds.
- the lignin in the black liquor is the main organic component and is present as a high mass colloid stabilized by ionized phenolic groups.
- Lignin is a phenylpropane polymer of amorphous structure comprising about 17 to about 30% of wood.
- Lignin is so closely associated with the cellulosic fibres and hemi-cellulose that makes up the balance of woody material that lignin can be separated from wood only by chemical reaction at high temperature, such as that used in the Kraft pulping process, wherein wood chips are digested with an aqueous alkaline solution of sodium hydroxide and hydrogen sulfide, known as white liquor. Normally, the black liquor, after separation of the wood fibers, is processed to remove organic materials and to recover and regenerate pulping chemicals. Lignin can be recovered from wood-processing wastes only in limited quantities.
- the lignin is a natural binder derivative of wood. Alkali lignin from both softwoods and hardwoods are useful in many products.
- Alkali lignin can also be used as adhesives for plywood, molding powers and formed insulating resins and as a reinforcing agent for rubber.
- Asphalt binders are widely used in different applications, such as asphalt-aggregate blends for road paving, asphalt fiber reinforced membranes for roofing and asphalt-water emulsions in surface treating both for paving and roofing. Problems for straight-run asphalt in those applications are the tendency to become brittle at low temperatures and to become soft at high temperatures, the tendency to flow under constant load at service temperatures and the tendency to phase separation during storage when mixed with other components .
- the present invention relates to compositions and methods for combining black liquor with selected petroleum-derived products. More specifically, this invention provides two separate processes for preparing lignin-based colloidal dispersions in lubricating or other petroleum-based oils.
- the lignin-oil colloidal dispersions prepared by either of such processes may be blended with bitumen to produce novel bituminous composition. Two embodiments of such procedures are described herein.
- the black liquor used in the invention may be that resulting from cooking wood in an alkaline solution in the soda or sulfate (Kraft) paper-making process.
- the asphalt employed in this invention can be any of the well known bituminous substances derived from petroleum, shale oil, coal tar and the like.
- the asphalt is prepared by vacuum distillation of a topped crude oil.
- the asphalt has a penetration at 25°C (as determined by ASTM D5) ranging for about 20 to about 400.
- the procedure involves essentially two steps.
- the black liquor is converted from its aqueous colloidal system to an anhydrous colloidal dispersion in a lubricating oil medium in which a surfactant, which may be an anionic surfactant, such as DDBSA (dodecylbenzene sulfuric acid) , is used to promote the provision of the anhydrous colloidal dispersion.
- a surfactant which may be an anionic surfactant, such as DDBSA (dodecylbenzene sulfuric acid)
- DDBSA dodecylbenzene sulfuric acid
- the anhydrous colloidal dispersion of lignin in oil may be mixed, in a second step, with asphalt bitumen, producing a unique combination, which is a novel bituminous composition.
- bitumen is treated with an inorganic acid, such as sulfuric acid, at elevated temperature to provide an acid-treated bitumen.
- the black alkaline liquor is then added slowly to the acid-treated bitumen under agitation for de-watering the black liquor at a controlled rate to form a stable, substantially anhydrous, colloidal dispersion of lignin in the bitumen, also to provide a novel bituminous composition.
- a lubricating oil is mixed with black liquor at temperatures below the water boiling point.
- a surfactant which may be DDBSA (dodecylbenzene sulfuric acid)
- DDBSA dodecylbenzene sulfuric acid
- the lubricating oil used in the first embodiment of the invention may be a re-refined waste motor oil or other convenient petroleum-based oil. Contaminants of waste motor oil, such as dirt, lead, arsenic and other harmful metals and chemicals, are removed from the waste motor oil to produce a clean base lubricating oil by the re-refining process.
- the lubricating oil may be a selected fraction of refined mineral oil used for lubrication of moving surfaces. Such fraction may range in consistency from thin liquid to grease-like substances. Usually, lubricating oils contain small amounts of additives to impart special properties, such as viscosity index and detergency.
- the surfactant or dispersing agent used in the process may typically be dodecylbenzene sulfuric acid (DDBSA) , although other anionic surfactants may be employed, if desired, such as fatty acid, linear alkyl sulfonates having 10 or more carbon atoms in the chain.
- DDBSA is benzene with dodecene, and the resulting dodecylbenzene is sulfonated.
- DDBSA may be neutralized with caustic soda from the alkaline black liquor or other convenient source to promote the detergency of the lubricating oil and to reduce surface tension in the mixture .
- a surfactant need not always be necessary, if the lubricating oil employed has a detergency high enough to ensure that a colloidal dispersion of the solid residue from the black liquor is achieved in the lubricating oil medium.
- the lignin-oil dispersion produced by either of these procedures may be smoothly blended with bitumen to provide the desired lignin-asphalt composition.
- bitumen first is treated with a strong mineral acid, such as sulfuric acid, at elevated temperature and then the alkaline black liquor is added to the treated bitumen at a controlled rate under agitation to effect de-watering of the black liquor to form a stable, substantially anhydrous, colloidal dispersion in the bitumen.
- a strong mineral acid such as sulfuric acid
- An inorganic acid is contacted with, or added to, the asphalt to form an acid treated asphalt.
- the acid addition shifts the asphalt structure from a sol to a gel, lowers the temperature susceptibility of the asphalt and improves the stability of the additive dispersion in the treated asphalt.
- black liquor is an aqueous alkaline system, it is critical that the acid not be added to the asphalt after addition of or with the black liquor.
- the acid is added slowly to the asphalt to avoid foaming, which may occur if all the acid were added at one time.
- the inorganic acid content of the asphalt resulting from the acid treatment is not critical, but normally is in the range between about 0.2 and about 3.5 wt%, preferably between about 0.5 and about 2.5 wt% of the asphalt.
- the inorganic acid is preferably selected from the group consisting of sulfuric acid, phosphoric acid, poly-phosphoric acid, phosphorous pentoxide, hydrochloric acid, and mixtures thereof.
- the sulfuric acid, phosphoric acid or poly-phosphoric acid are preferred inorganic acids, with the sulfuric acid being particularly preferred.
- the alkaline black liquor is then added slowly to the acid-treated bitumen at an elevated temperature, typically around 100°C, under agitation for a certain period of time to permit dewatering of the black liquor to occur while the solids are incorporated into the bitumen.
- the temperature of the final composition next is increased above the boiling point of water, typically up to around 160°C until residual water is completely evaporated off to 7
- Example 1 This Example illustrates the first embodiment of the invention in which black liquor first dispersed in a lubricating oil and then in bitumen.
- Mass of analyzed sample of reclaimed lube oil was determined following the test method of ASTM 4124-92.
- Base asphalt (or bitumen) used in the present invention were selected from three different degrades: AC-5 having an absolute viscosity of around 500 poises, 185/100 having a 25°C penetration range from 85 dmm to 100 dmm and 1120/150 having a 25°C penetration range from 120 dmm to 150 dmm.
- the non-aqueous dispersing system of black liquor/lube-oil produced as described in the Table 1 was dispersed into hot liquid asphalt at about 160°C respectively to form a very fine dispersion mixture.
- the stability of these lignin based bituminous mixtures during hot storage at elevated temperature was evaluated using a conditioned tube test.
- the conditioning procedure consists of placing approximately 70g of the mixture in H" aluminum tubes and storing such tubes in a vertical position at 165°C in an oven for 48 hrs. Following hot storage, a viscosity ratio was determined by comparing the viscosity of the mixture tested at 135°C from the bottom section of the sample and from the top section of the sample in the tube. A ratio in the range of 0.80 to 1.20 is generally considered acceptable with respect to separation of the dispersed phase.
- the testing results on eight compositions are shown in the following Table 2. The results indicate that the lignin based solid dispersion in asphalt binder are quite stable.
- This Example illustrates the second embodiment of the invention in which bitumen first is acidified.
- Sulfuric acid 95 to 98% H 2 S0 4
- results of dispersion and stability determinations are also shown below in the following Table 3.
- the results shown in Table 3 indicate that products of formulation containing 0.8 wt% acid and 0 to 30 wt%, preferably 15 to 25 wt% black liquor, based on the amount of asphalt, had good stability.
- the present invention provides novel procedures for the stable dispersion of lignin components of black liquor in bitumen. Modifications are possible within the scope of the invention.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A lignin based colloidal dispersion into lubricating oil or bitumen is prepared from black liquor residue. In one process, in the first step, the black liquor is converted from its aqueous colloidal system to an anhydrous colloidal dispersion in a re-refined lubricating oil medium in which a surfactant, such as DDBSA (dodecylbenzene sulfuric acid), is used to promote the colloidal dispersion. In second step, bitumen is mixed with the product obtained from said first step. In another process, bitumen first is treated with an inorganic acid, such as sulfuric acid, at elevated temperature. The alkaline black liquor is then added slowly to the acid-treated bitumen under agitation for de-watering at a controlled rate to form a stable, substantially anhydrous, colloidal dispersion in the bitumen.
Description
TITLE OF INVENTION LIGNIN BASED COLLOIDAL COMPOSITIONS
FIELD OF INVENTION
The present invention relates to the processing of black liquor and the preparation of bitumen compositions containing black liquor.
BACKGROUND TO THE INVENTION
Black liquor is an aqueous alkaline pulping residue produced in Kraft pulping of wood chips in a pulp mill to provide wood fibers for paper-making. Black liquor generally contains about 55 to 65% solids comprising lignin, sodium salts of poly-saccharinic acids, organic and inorganic sulfides and carbonates and many other compounds. The lignin in the black liquor is the main organic component and is present as a high mass colloid stabilized by ionized phenolic groups. Lignin is a phenylpropane polymer of amorphous structure comprising about 17 to about 30% of wood. Lignin is so closely associated with the cellulosic fibres and hemi-cellulose that makes up the balance of woody material that lignin can be separated from wood only by chemical reaction at high temperature, such as that used in the Kraft pulping process, wherein wood chips are digested with an aqueous alkaline solution of sodium hydroxide and hydrogen sulfide, known as white liquor. Normally, the black liquor, after separation of the wood fibers, is processed to remove organic materials and to recover and regenerate pulping chemicals. Lignin can be recovered from wood-processing wastes only in limited quantities. The lignin is a natural binder derivative of wood. Alkali lignin from both softwoods and hardwoods are useful in many products. They are used as stabilizers for asphalt emulsions, modifiers and extenders for latex emulsions, compounding agents in vinyl plastics, soil conditioners, binders in printing inks, wood stains, protective colloids in soap emulsions, dispersing agents
for clay, fire foam stabilizers, drilling mud additives, insecticide dispersants, absorbers in storage batteries and foundry sand binders. Alkali lignin can also be used as adhesives for plywood, molding powers and formed insulating resins and as a reinforcing agent for rubber. Asphalt binders (or bitumen) are widely used in different applications, such as asphalt-aggregate blends for road paving, asphalt fiber reinforced membranes for roofing and asphalt-water emulsions in surface treating both for paving and roofing. Problems for straight-run asphalt in those applications are the tendency to become brittle at low temperatures and to become soft at high temperatures, the tendency to flow under constant load at service temperatures and the tendency to phase separation during storage when mixed with other components .
Various approaches have been used for the purpose of improving asphalt compositions to address these problems. For instance, polymers have been utilized to improve the high and low temperature characteristics of asphalt compositions, as well as to improve their toughness and durability. Air blowing of straight-run asphalt has been used to improve stiffness and dimensional stability for hot applied roofing systems. The asphalt may be treated with acid to improve its compatibility with the polymeric additives. Lignin or lignin based additives have been widely used to emulsify asphalt to achieve a stable dispersion of asphalt in aqueous medium. Black liquor is an aqueous colloidal system in which ample lignin is present. However, means have not been previously disclosed whereby a stable dispersion of lignin in asphalt can be achieved by combining black liquor with hot liquid asphalt. When the black liquor is added to the bitumen and dispersed with agitation into molten asphalt cement, de-watering of the black liquor
occurs while lignin and other salts in the black liquor tend to form large, rigid aggregates which separate from the liquid asphalt and subsequently strongly resist dispersion in the asphalt. It is one objective of the present invention to develop a process or processes whereby liquor-solid pulping residue (black liquor) can be converted from one in which water is the dispersing and plasticizing agent to one in which water is replaced by oil, achieving a dispersion in which a lignin based colloidal particulate phase is stably maintained. It is another objective to provide a lignin-oil dispersion which can be smoothly blended with liquid asphalt to produce a stable, homogeneous dispersion. SUMMARY OF INVENTION
The present invention relates to compositions and methods for combining black liquor with selected petroleum-derived products. More specifically, this invention provides two separate processes for preparing lignin-based colloidal dispersions in lubricating or other petroleum-based oils. The lignin-oil colloidal dispersions prepared by either of such processes may be blended with bitumen to produce novel bituminous composition. Two embodiments of such procedures are described herein. The black liquor used in the invention may be that resulting from cooking wood in an alkaline solution in the soda or sulfate (Kraft) paper-making process.
The asphalt employed in this invention can be any of the well known bituminous substances derived from petroleum, shale oil, coal tar and the like. Commonly, the asphalt is prepared by vacuum distillation of a topped crude oil. Preferably, the asphalt has a penetration at 25°C (as determined by ASTM D5) ranging for about 20 to about 400.
In a first embodiment of the invention, the
procedure involves essentially two steps. In the first step, the black liquor is converted from its aqueous colloidal system to an anhydrous colloidal dispersion in a lubricating oil medium in which a surfactant, which may be an anionic surfactant, such as DDBSA (dodecylbenzene sulfuric acid) , is used to promote the provision of the anhydrous colloidal dispersion. The process may be effected under low shear conditions.
The anhydrous colloidal dispersion of lignin in oil may be mixed, in a second step, with asphalt bitumen, producing a unique combination, which is a novel bituminous composition.
In another embodiment of the invention, the procedure again involves essentially two steps. First, bitumen is treated with an inorganic acid, such as sulfuric acid, at elevated temperature to provide an acid-treated bitumen. The black alkaline liquor is then added slowly to the acid-treated bitumen under agitation for de-watering the black liquor at a controlled rate to form a stable, substantially anhydrous, colloidal dispersion of lignin in the bitumen, also to provide a novel bituminous composition.
DETAILED DESCRIPTION OF THE INVENTION Referring first to the first embodiment of the invention, a lubricating oil is mixed with black liquor at temperatures below the water boiling point. A surfactant, which may be DDBSA (dodecylbenzene sulfuric acid) , is selected to be added to the mixture to facilitate the colloidal dispersion of black liquor in the lubricating oil while de-watering is gradually carried out at an elevated temperature. The resulting cream-like paste product is miscible with hot liquid asphalt at any ratio to form a novel bituminous composition. The lubricating oil used in the first embodiment of the invention may be a re-refined waste motor oil or
other convenient petroleum-based oil. Contaminants of waste motor oil, such as dirt, lead, arsenic and other harmful metals and chemicals, are removed from the waste motor oil to produce a clean base lubricating oil by the re-refining process.
The lubricating oil may be a selected fraction of refined mineral oil used for lubrication of moving surfaces. Such fraction may range in consistency from thin liquid to grease-like substances. Usually, lubricating oils contain small amounts of additives to impart special properties, such as viscosity index and detergency.
The surfactant or dispersing agent used in the process may typically be dodecylbenzene sulfuric acid (DDBSA) , although other anionic surfactants may be employed, if desired, such as fatty acid, linear alkyl sulfonates having 10 or more carbon atoms in the chain. DDBSA is benzene with dodecene, and the resulting dodecylbenzene is sulfonated. DDBSA may be neutralized with caustic soda from the alkaline black liquor or other convenient source to promote the detergency of the lubricating oil and to reduce surface tension in the mixture .
However, a surfactant need not always be necessary, if the lubricating oil employed has a detergency high enough to ensure that a colloidal dispersion of the solid residue from the black liquor is achieved in the lubricating oil medium.
The lignin-oil dispersion produced by either of these procedures may be smoothly blended with bitumen to provide the desired lignin-asphalt composition.
Referring now to the second embodiment of the invention, the bitumen first is treated with a strong mineral acid, such as sulfuric acid, at elevated temperature and then the alkaline black liquor is added to the treated bitumen at a controlled rate under
agitation to effect de-watering of the black liquor to form a stable, substantially anhydrous, colloidal dispersion in the bitumen.
An inorganic acid is contacted with, or added to, the asphalt to form an acid treated asphalt. In general, the acid addition shifts the asphalt structure from a sol to a gel, lowers the temperature susceptibility of the asphalt and improves the stability of the additive dispersion in the treated asphalt. Since black liquor is an aqueous alkaline system, it is critical that the acid not be added to the asphalt after addition of or with the black liquor.
Preferably, the acid is added slowly to the asphalt to avoid foaming, which may occur if all the acid were added at one time. The inorganic acid content of the asphalt resulting from the acid treatment is not critical, but normally is in the range between about 0.2 and about 3.5 wt%, preferably between about 0.5 and about 2.5 wt% of the asphalt. Although a wide variety of inorganic acids can be used for treatment of the asphalt, the inorganic acid is preferably selected from the group consisting of sulfuric acid, phosphoric acid, poly-phosphoric acid, phosphorous pentoxide, hydrochloric acid, and mixtures thereof. The sulfuric acid, phosphoric acid or poly-phosphoric acid are preferred inorganic acids, with the sulfuric acid being particularly preferred.
Following acid addition, the alkaline black liquor is then added slowly to the acid-treated bitumen at an elevated temperature, typically around 100°C, under agitation for a certain period of time to permit dewatering of the black liquor to occur while the solids are incorporated into the bitumen. The temperature of the final composition next is increased above the boiling point of water, typically up to around 160°C until residual water is completely evaporated off to
7
form a stable, substantially anhydrous, colloidal lignin dispersion in the bitumen.
EXAMPLES Example 1: This Example illustrates the first embodiment of the invention in which black liquor first dispersed in a lubricating oil and then in bitumen. General Procedure:
Black liquor and DDBSA were mixed at room temperature in specific proportions under stirring for 20 to 30 min to form a mixture. Re-refined waste lube- oil was added into the mixture at room temperature to a desired concentration and stirred another about 20 min. The resulting mixture was heated slowly to about 160° to 180°C for about 2 to 3 hours under stirring until water- free. During this step, the viscosity of the system exhibited complex phenomena because a raising of the temperature resulted in reduced viscosity while water loss resulted in increased viscosity. Accordingly, the temperature and time for de-watering must be controlled. Specific Experiments:
16 Kg of DDBSA was added to 266 g of black liquor (ca. 60% solid content) and stirred at room temperature for 20 to 30 min. 184 g of reclaimed lube oil were added and stirred again at room temperature for 20 to 30 min. The temperature of the mixture was slowly raised from room temperature to 170°C for 2 to 3 hours to de-water the composition. After de-watering and cooling, about 332 g sample was obtained. The sample was a black colored paste and water-free and was easily dispersed into asphalt at any ratio. This sample was designated as B-14, seen in Table 1.
Different black liquor/lube oil formulations have been prepared following the above procedure and the data are presented in the following Table 1:
o
TABLE 1 i- NON-AQUEOUS DISPERSING SYSTEM OF BLACK LIQUOR/LUBE OIL
Sample Black liquor DDBSA Lube Oil Product Wt. Code g g wt% g wt% g
B-13 246 24 4.6 254 48.5 410
B-14 266 16 3.4 184 39.5 332
B-15 218 6.0 1.94 180 44.6 302
B-19 336 10 2.15 120 25.8 308
B-20 460 14 2.35 122 20.5 372
RB-30 590 (1 part) 17.7 (0.03 part) 413 (0.7 part) co
Note: Mass of analyzed sample of reclaimed lube oil (recovered from engine oil) was determined following the test method of ASTM 4124-92.
n H π > VO SO
©o
Base asphalt (or bitumen) used in the present invention were selected from three different degrades: AC-5 having an absolute viscosity of around 500 poises, 185/100 having a 25°C penetration range from 85 dmm to 100 dmm and 1120/150 having a 25°C penetration range from 120 dmm to 150 dmm. The non-aqueous dispersing system of black liquor/lube-oil produced as described in the Table 1 was dispersed into hot liquid asphalt at about 160°C respectively to form a very fine dispersion mixture. The stability of these lignin based bituminous mixtures during hot storage at elevated temperature was evaluated using a conditioned tube test. The conditioning procedure consists of placing approximately 70g of the mixture in H" aluminum tubes and storing such tubes in a vertical position at 165°C in an oven for 48 hrs. Following hot storage, a viscosity ratio was determined by comparing the viscosity of the mixture tested at 135°C from the bottom section of the sample and from the top section of the sample in the tube. A ratio in the range of 0.80 to 1.20 is generally considered acceptable with respect to separation of the dispersed phase. The testing results on eight compositions are shown in the following Table 2. The results indicate that the lignin based solid dispersion in asphalt binder are quite stable.
O
TABLE 2 SO STABILITY OF THE BLACK LIQUOR/LUBE OIL BLEND (BLB) IN HOT ASPHALT m
Asphalt BLB Viscosity, cp at 135°C
Code Name - (g) Code (g) (%) Top/Bottom Stability Index*
AB5-16 AC5 368 B-13 38 10 455/463 0.98
B14-85-10 185/100 90 B-14 10 10 387.5/432.5 0.90
B14-85-20 185/100 80 B-14 20 20 450/465 0.97
B14-85-30 185/100 70 B-14 30 30 435/500 0.87
B15-A 1120/150 70 B-15 30 30 825/845 0.97
B15-B 1120/150 85 B-15 15 15 257/265 0.97
B20-20 1120/150 80 B-20 20 20 740/802.5 0.92
RB30-30 1120/150 80 RB-30 20 20 405/475 0.85
Note: (1) In the better formulations of the non-aqueous dispersing system, an appropriate composition was a lube oil content of more than 20% and DDBSA content of greater than 2%. (2) DDBSA is dodecylbenzene sulfuric acid. Stability Index = Viscosity at top
Viscosity at bottom -o O H
O
>so o
©o in in
11
Example 2 :
This Example illustrates the second embodiment of the invention in which bitumen first is acidified. General Procedure: Sulfuric acid (95 to 98% H2S04) was added into hot asphalt AC-5 at 100° to 110°C under stirring (800 to 1000 RPM) for 20 to 30 mins. to form an acid-modified asphalt, followed by addition of aqueous black liquor (c.a. 60% solid content) into the acid-modified asphalt, according to the following procedure.
(1) While stirring at 800 to 1000 RPM, the acid was added into asphalt at 100° to 110°C for 20 to 30 min. and acid-modified asphalt was obtained.
(2) After 20 to 30 min., black liquor was added to the acid-modified asphalt at 105° to 115°C for 30 to 40 min., then maintained for 1 to 2 hours for dewatering.
(3) The temperature was slowly increased to 170°C while stirring for 1 to 2 hours to effect further dewatering.
(4) The composition was allowed to cool and was sampled for stability.
Specific Experiments:
To 392 g of asphalt AC-5 were added 3.14 g of H2S04 (0.8% AC-5) at 100° to 110°C under 800 to 1000 RPM stirring for 20 min. The acidified asphalt was maintained at 100° to 110°C and black liquor 84 g (22% AC-5) was added over about 30 min., and then the composition was maintained for 1 to 2 hrs at 105° to 115°C to dewater the black liquor. The temperature was raised to 170°C while stirring to effect further dewatering. The product was then cooled to provide 436 g of product (loss mass 43 g) . The stability index determined on this sample (AC-B-18) was 0.94, shown in Table 3.
12
Results of dispersion and stability determinations are also shown below in the following Table 3. The results shown in Table 3 indicate that products of formulation containing 0.8 wt% acid and 0 to 30 wt%, preferably 15 to 25 wt% black liquor, based on the amount of asphalt, had good stability.
SO
TABLE 3 SO t~ EXPERIMENTAL FORMULATIONS AND STABILITY in
Asphalt Acid Black Liquor Viscosity cp after 48 hrs (AC-5) storage at 160°C
Code (g) (g) (%) (g) (%) Top Bottom Stability Index
AC-B-24 374 0 0 112 30 Sediment appeared11'
AC-B-11 472 2.4 0.5 94 20 413 550 0.75
AC-B-10 362 4.0 1.1 72 20 298 310 0.96
AC-B-18 392 3.14 0.8 84 22 338 358 0.94
AC-B-25 294 2.35 0.8 59 20 312.5 317.5 0.98
AC-B-26 288 2.3 0.8 72 25 360 342.5 1.05
AC-B-19 360 2.94 0.8 110 30 270 598 0.45
AC-B-23 380 3.8 1.0 114 30 290 907.5 0.32
AC-B-21 360 4.32 1.2 108 30 377.5 360 1.05
AC-B-22 373 3.73 1.0 149 40 300 402.5 0.75
AC-B-20 380 3.0 0.8 190 50- 267.5 1060 0.25
Note: (1) No measurement was possible. n
H o >
SO ©
© m
14
SUMMARY OF THE DISCLOSURE
In summary of this disclosure, the present invention provides novel procedures for the stable dispersion of lignin components of black liquor in bitumen. Modifications are possible within the scope of the invention.
Claims
15
What I claim is:
1. A bituminous composition, comprising bitumen, and dewatered lignin-containing spent alkaline pulping liquor stably dispersed therein.
2. The bituminous composition of claim 1 wherein said dewatered spent alkaline pulping liquor is present in an amount up to about 50 wt% of the bitumen.
3. The bituminous composition of claim 2 wherein said dewatered spent alkaline pulping liquor is present in an amount of from about 5 to about 25 wt% of the bitumen. . The bituminous composition of claim 1 wherein said dewatered spent alkaline pulping liquor comprises an anhydrous colloidal dispersion of lignin in a lubricating oil.
5. The bituminous composition of claim 1 wherein said dewatered spent alkaline pulping liquor comprises a stable, substantially anhydrous, colloidal dispersion of lignin in the bitumen.
6. The bituminous composition of claim 1 wherein the spent alkaline pulping liquor is black liquor from a Kraft pulp mill.
7. A method of producing a composition, which comprises : converting an aqueous colloidal dispersion of liquor in spent pulping liquor to an anhydrous colloidal dispersion of lignin in a lubricating oil.
8. The method of claim 7 wherein said converting step is effected by: mixing a lubricating oil with the spent pulping liquor, and dewatering the mixture so formed at an elevated temperature to form a cream-like paste compatible with hot bitumen.
16
9. The method of claim 8 wherein said mixing step is effected in the presence of a surfactant to facilitate colloidal dispersion of the spent pulping liquor in the lubricating oil.
10. The method of claim 9 wherein said surfactant is an anionic surfactant.
11. The method of claim 10 wherein the anionic surfactant is a fatty acid linear alkyl sulfonate.
12. The method of claim 7 including blending the anhydrous colloidal dispersion of lignin in a lubricating oil with bitumen.
13. The method of claim 7 wherein said spent pulping liquor is black liquor from a Kraft pulp mill.
14. The method of claim 7 wherein the spent pulping liquor is present in an amount of about 10 to about 60 wt% of the composition.
15. The method of claim 14 wherein the black liquor is present in an amount of about 25 to 40 wt%.
16. A method of producing a bituminous composition, which comprises: converting an aqueous colloidal dispersion of lignin in spent alkaline pulping liquor to an anhydrous colloidal dispersion of lignin in a lubricating oil, and mixing said anhydrous colloidal dispersion of lignin with bitumen.
17. The method of claim 16 wherein said spent alkaline pulping liquor is black liquor from a Kraft pulp mill.
18. The method of claim 16 which is effected by stressing at elevated temperature.
19. The method of claim 18 wherein said elevated temperature is about 100° to about 180°C.
20. The method of claim 19 wherein said temperature is about 110° to about 160°C
21. A method of producing a bituminous composition which comprises: treating bitumen with an inorganic acid at an
17
elevated temperature to provide acid-treated bitumen, slowly adding to the acid-treated bitumen a lignin- containing spent alkaline pulping liquor, while agitating the bitumen to effect controlled dewatering of the spent pulping liquor to form a stable, substantially anhydrous colloidal dispersion of lignin in the bitumen.
22. The method of claim 21 wherein said inorganic acid treatment of bitumen is effected to convert the bitumen structure from a sol to a gel, lower the temperature susceptibility of the asphalt and improve the stability of the additive dispersion in the treated bitumen.
23. The method of claim 22 wherein said inorganic acid is added slowly to the bitumen at an elevated temperature to avoid foaming to provide an inorganic acid content of said bitumen of about 0.2 to about 3.5 wt%.
24. The method of claim 23 wherein said inorganic acid content is from about 0.5 to about 2.5 wt% of the bitumen.
25. The method of claim 21 wherein said inorganic acid is sulfuric acid.
26. The method of claim 21 wherein said addition step is effected by: initially slowly adding the spent alkaline pulping liquor to the acid-treated bitumen at substantially water boiling temperature while agitating the bitumen to effect an initial dewatering of the alkaline spent pulping liquor, and subsequently increasing the temperature of the bitumen above the water boiling point to effect a further dewatering of the bitumen to form the stable, substantially anhydrous, colloidal dispersion of lignin in the bitumen.
27. The method of claim 21 wherein said spent alkaline pulping liquor is black liquor from a Kraft pulp mill operation.
18
28. The method of claim 21 wherein said elevated temperature is about 100° to about 180°C.
29. The method of claim 28 wherein said temperature is about 110° to about 160°C.
30. The method of claim 21 wherein the spent pulping liquor is present in an amount of about 5 to about 50 wt% of the composition.
31. The method of claim 21 wherein the spent pulping liquor is present in an amount of about 10 to about 30 wt%.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7554698P | 1998-02-23 | 1998-02-23 | |
| US75546P | 1998-02-23 | ||
| PCT/CA1999/000155 WO1999042526A1 (en) | 1998-02-23 | 1999-02-22 | Lignin based colloidal compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1058713A1 true EP1058713A1 (en) | 2000-12-13 |
Family
ID=22126470
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99906000A Withdrawn EP1058713A1 (en) | 1998-02-23 | 1999-02-22 | Lignin based colloidal compositions |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP1058713A1 (en) |
| AU (1) | AU2606299A (en) |
| CA (1) | CA2321735A1 (en) |
| WO (1) | WO1999042526A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2018363835A1 (en) * | 2017-11-13 | 2020-04-16 | Asfalt Kennis Centrum B.V. | Lignin-based bio-asphalt |
| EP4008752A1 (en) * | 2020-12-03 | 2022-06-08 | Peab Asfalt AB | Method for producing an asphalt mix containing lignin and an asphalt composition produced thereby |
| CN113527778B (en) * | 2021-08-09 | 2022-12-02 | 南京工业大学 | Preparation method and application of nano lignin latex |
| SE2330210A1 (en) * | 2023-05-10 | 2024-11-11 | Stora Enso Oyj | Process for producing a binder for a warm mix asphalt composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3956002A (en) * | 1974-03-18 | 1976-05-11 | Westvaco Corporation | Anionic bituminous emulsions |
| US4293459A (en) * | 1979-06-07 | 1981-10-06 | American Can Company | Asphalt emulsion-conditioner |
-
1999
- 1999-02-22 EP EP99906000A patent/EP1058713A1/en not_active Withdrawn
- 1999-02-22 CA CA002321735A patent/CA2321735A1/en not_active Abandoned
- 1999-02-22 AU AU26062/99A patent/AU2606299A/en not_active Abandoned
- 1999-02-22 WO PCT/CA1999/000155 patent/WO1999042526A1/en not_active Ceased
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9942526A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2321735A1 (en) | 1999-08-26 |
| WO1999042526A1 (en) | 1999-08-26 |
| AU2606299A (en) | 1999-09-06 |
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