US20070199476A1 - Bitumen composition - Google Patents
Bitumen composition Download PDFInfo
- Publication number
- US20070199476A1 US20070199476A1 US11/558,711 US55871106A US2007199476A1 US 20070199476 A1 US20070199476 A1 US 20070199476A1 US 55871106 A US55871106 A US 55871106A US 2007199476 A1 US2007199476 A1 US 2007199476A1
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- United States
- Prior art keywords
- paraffin wax
- bitumen
- wax
- composition according
- pen
- Prior art date
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- 239000010426 asphalt Substances 0.000 title claims abstract description 75
- 239000000203 mixture Substances 0.000 title claims abstract description 65
- 239000012188 paraffin wax Substances 0.000 claims abstract description 41
- 239000001993 wax Substances 0.000 claims abstract description 37
- 239000000654 additive Substances 0.000 claims description 50
- 235000019271 petrolatum Nutrition 0.000 claims description 46
- 230000000996 additive effect Effects 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 21
- 238000009835 boiling Methods 0.000 claims description 7
- 230000035515 penetration Effects 0.000 claims description 6
- 238000004821 distillation Methods 0.000 claims description 4
- 238000004517 catalytic hydrocracking Methods 0.000 claims description 3
- 239000000446 fuel Substances 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000000047 product Substances 0.000 description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000005864 Sulphur Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 239000000945 filler Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 235000019738 Limestone Nutrition 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000006028 limestone Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241001248539 Eurema lisa Species 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 229920000034 Plastomer Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- -1 poly ethylene Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 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
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
- C08L91/08—Mineral waxes
Definitions
- the invention is directed to a bitumen composition comprising a paraffin wax additive.
- the invention is also directed to the paraffin wax additive itself.
- Bitumen compositions are widely applied as road surfaces for motor vehicles and airplanes. These compositions are also referred to as asphalt and comprise bitumen and aggregates such as sand, gravel, grit or the like. Additives are widely applied to improve certain properties of the bitumen composition for use as road surfaces.
- U.S. Pat. No. 6,588,974, WO-A-0216499 and AU-B-200137219 disclose a bitumen composition containing a Fischer-Tropsch paraffin (FT paraffin) as an additive.
- FT paraffin Fischer-Tropsch paraffin
- the Fischer-Tropsch paraffin additive is a mixture of more than 90% n-alkanes and the remainder being iso-alkanes.
- An advantage of adding the FT paraffin additive is that the additive lowers the viscosity of the bitumen composition at elevated, e.g. 135 and 180° C, temperatures. This is advantageous because this is the temperature at which the bitumen mixture is used when making road surfaces. In other words the additive improves the workability of the bitumen composition.
- FT paraffin has a chain length of between 30 and 100 carbon atoms.
- AU-B-200137219 exemplifies a commercially available Fischer-Tropsch paraffin additive as SASOBIT (SASOBIT is a Registered Trademark).
- SASOBIT is a Registered Trademark.
- the congealing range according to DIN-ISO 02207 is ⁇ 99° C. as published by Sasol Wax GmbH, Hamburg.
- a problem encountered by the addition of the FT paraffin wax additives is that the Fraass point remains the same or even increases when the content of additives increases.
- the Fraass point (EN12593) is indicative for the brittleness of the bitumen mixture at low temperatures.
- a sample of bituminous binder is applied on a metal plate. This plate is submitted to a constant cooling rate and flexed repeatedly until the binder layer breaks. The temperature at which the first crack appears is reported as the Fraass breaking point.
- a low Fraass point is for example desirable when road surfaces are made in areas having a cold climate.
- the invention is therefore directed to a bitumen composition
- a bitumen composition comprising a paraffin wax having a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
- the soft paraffin wax additive of the present invention has a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
- the congealing point of the above wax is above 90° C.
- the softness of the wax can be influenced by adjusting the process conditions of the manufacturing process and/or by blending soft wax and hard wax, wherein the hard wax can be a more normal paraffinic wax such as for example SASOBIT or the Sarawax SX100 or Sarawax SX105 type wax products as obtainable from Shell MDS Malaysia Sdn Bhd.
- the hard wax can be a more normal paraffinic wax such as for example SASOBIT or the Sarawax SX100 or Sarawax SX105 type wax products as obtainable from Shell MDS Malaysia Sdn Bhd.
- Suitable bitumens include those with penetrations in the range of 1 to 450 mm/10 as determined in accordance with EN 1426.
- the softening point of suitable bitumens may range from 30 to 130° C., preferably, 40 to 100° C. as determined in accordance with EN 1427.
- the penetration index of suitable bitumens may range between +9 and ⁇ 3.
- the viscosity at 60° C. may be 10 to 20,000 Pas.
- the content of soft paraffin wax additive in the bitumen composition according to the invention may be up to 20 wt %, more preferably between 0.1 to 20 wt %, even more preferably between 0.5 to 10 wt %.
- the Fraass temperature decreases, even at higher contents of said partly isomerized paraffin wax.
- the substantially normal paraffin wax like for example the commercial SASOBIT product, is used in a high content, the Fraass temperature does not improve with respect to the starting bitumen.
- the bitumen composition according to the invention may be employed as a binder for aggregates to form an asphalt composition.
- the aggregates employed in such compositions include conventional aggregates such as granite.
- fillers of, for example, limestone and cellulose may also be included in the bituminous composition. Sand and dust may also be present.
- the bitumen composition may form 1 to 20 wt %, preferably, 2 to 15 wt %, more preferably, 4 to 10 wt %, and most preferably, 4 to 7 wt % of the overall asphalt composition.
- the aggregate content of the overall composition may be more than 50 wt %, preferably, more than 60 wt %, even more preferably, more than 70 wt % for example, 75 to 90 wt %.
- the remainder of the asphalt composition may comprise sand, cellulose and/or limestone.
- bitumen composition according to the present invention may also be used as part of so-called joint sealants, which are for example used to fix concrete elements in airport surfaces, or as part of a roofing felt composition.
- Paraflint H1 is obtainable from Sasol-Moore and Munger.
- the Sarawax products are obtainable from Shell MDS Malaysia Sdn Bhd.
- the congealing point and the PEN at 43° C. of such a blended wax has the properties as described above.
- a very suitable soft paraffin wax can be obtained as a by-product of the following process wherein middle distillates are prepared from a Fischer-Tropsch wax.
- This process comprises the steps of (a) hydrocracking/hydroisomerisating a Fischer-Tropsch product, (b) performing one or more distillate separations on the effluent of step (a) to obtain a middle distillate fuel fraction and a soft paraffin wax additive having an initial boiling point of between 500 and 600° C.
- the additive is preferably obtained as a residual fraction in a vacuum distillation step.
- the PEN value at 43° C. of the wax as obtained by this process may be reduced if required by blending this wax with a wax fraction isolated by distillation from the starting Fischer-Tropsch product.
- This fraction preferably hydrogenated in order to remove oxygenates and olefins and having a congealing point of between 90 and 120° C., is a substantially normal paraffin wax having a lower PEN value at 43° C. By blending this component with the softer wax a controlled value for the PEN at 43° C. may be obtained.
- the Fischer-Tropsch product comprises a C 20 + fraction having an ASF-alpha value (Anderson-Schulz-Flory chain growth factor) of at least 0.925, preferably at least 0.935, more preferably at least 0.945, even more preferably at least 0.955.
- ASF-alpha value Anderson-Schulz-Flory chain growth factor
- the Fischer-Tropsch product will contain no or very little sulphur and nitrogen containing compounds. This is typical for a product derived from a Fischer-Tropsch reaction, which uses synthesis gas containing almost no impurities. Sulphur and nitrogen levels will generally be below the detection limits, which are currently 5 ppm for sulphur and 1 ppm for nitrogen. The soft paraffin wax additive will consequently also have such low sulphur and nitrogen levels.
- the process conditions and other directions of how to perform the above process have been reported earlier by applicant in WO-A-2004009739 which publication is hereby incorporated by reference.
- the soft wax as obtained from one of the above Fischer-Tropsch processes is suitably transformed into a form in which handling of the product is facilitated.
- Suitable forms are containers filled with solid wax product, which containers can be heated at the location of use and wherein the wax is added to the bitumen in its liquid state. Heated containers containing the wax in its liquid state may also be used.
- the wax may also be provided as pellets, extrudates, flakes or powder. In order to prevent the wax particles from sticking to each other, silica powder and the like may be added to provide a less sticky surface of the wax particles.
- Example 1 was repeated using a 70/100 pen grade bitumen having the properties listed in Table 2. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 4.
- Example 1 was repeated using SASOBIT having the properties as listed in Table 1. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 3.
- Example 2 was repeated using SASOBIT having the properties as listed in Table 1. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 4.
- Example 16 To the 35/50 pen grade bitumen of Example 16 wt % of a 50/50 wt % blend of the soft wax additive and the SASOBIT (see Table 1) were added. The PEN at 43° C. (0.1 mm) of the resulting wax blend was 39.
- the increase in softening point relative to the starting bitumen was 24.6° C. and the decrease in Fraass temperature relative to the starting bitumen was 2° C.
- Table 3 and Table 4 show that at a given concentration and for a given bitumen, the additive of the invention leads to the lowest Fraass breaking point values for the corresponding bituminous blend when compared to the unmodified and the SASOBIT modified bitumen.
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- Polymers & Plastics (AREA)
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- Structural Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Civil Engineering (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Road Paving Structures (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Abstract
A novel bitumen composition comprising a paraffin wax, wherein the wax has a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
Description
- This application claims the benefit of European Patent Application No. 05292400.8, filed Nov. 10, 2005, which is incorporated herein by reference.
- The invention is directed to a bitumen composition comprising a paraffin wax additive. The invention is also directed to the paraffin wax additive itself.
- Bitumen compositions are widely applied as road surfaces for motor vehicles and airplanes. These compositions are also referred to as asphalt and comprise bitumen and aggregates such as sand, gravel, grit or the like. Additives are widely applied to improve certain properties of the bitumen composition for use as road surfaces.
- U.S. Pat. No. 6,588,974, WO-A-0216499 and AU-B-200137219 disclose a bitumen composition containing a Fischer-Tropsch paraffin (FT paraffin) as an additive. According to U.S. Pat. No. 6,588,974 the Fischer-Tropsch paraffin additive is a mixture of more than 90% n-alkanes and the remainder being iso-alkanes. An advantage of adding the FT paraffin additive is that the additive lowers the viscosity of the bitumen composition at elevated, e.g. 135 and 180° C, temperatures. This is advantageous because this is the temperature at which the bitumen mixture is used when making road surfaces. In other words the additive improves the workability of the bitumen composition.
- According to these publications the FT paraffin has a chain length of between 30 and 100 carbon atoms. AU-B-200137219 exemplifies a commercially available Fischer-Tropsch paraffin additive as SASOBIT (SASOBIT is a Registered Trademark). According to the product specifications dated Nov. 11, 2003 for SASOBIT, the congealing range according to DIN-ISO 02207 is ≦99° C. as published by Sasol Wax GmbH, Hamburg.
- A problem encountered by the addition of the FT paraffin wax additives is that the Fraass point remains the same or even increases when the content of additives increases. The Fraass point (EN12593) is indicative for the brittleness of the bitumen mixture at low temperatures. In this test a sample of bituminous binder is applied on a metal plate. This plate is submitted to a constant cooling rate and flexed repeatedly until the binder layer breaks. The temperature at which the first crack appears is reported as the Fraass breaking point. A low Fraass point is for example desirable when road surfaces are made in areas having a cold climate.
- Applicants have now discovered that the Fraass point can be lowered when a slightly isomerized paraffin wax is used instead of a highly normal paraffin wax. Applicants have further found that the viscosity at elevated temperatures is lowered comparable to when using the state of the art normal paraffin FT paraffin additive.
- The invention is therefore directed to a bitumen composition comprising a paraffin wax having a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
- The invention is also directed to a paraffin wax having a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5 mm in suitable form for use as a bitumen additive. This additive will also be referred to in this application as a soft paraffin wax additive.
- The invention is also directed to a process to lower the Fraass point of a bitumen composition by adding to a bitumen composition a paraffin wax having a congealing point of between 85 and 120° C., as determined by ISO 2207, and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
- The soft paraffin wax additive of the present invention has a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5. Preferably the congealing point of the above wax is above 90° C.
- The soft paraffin wax additive having generally the combination of said congealing point and PEN values is constituted for a major portion of iso-paraffins. The quantity of iso-paraffins is however difficult to quantify in this boiling range. For this reason these more easily quantifiable properties are used.
- In order to reduce the Fraass temperature significantly, it is preferred to use a soft wax having a PEN at 43° C. expressed in 0.1 mm of greater than 7, more preferably greater than 8 and even more preferably greater than 10. The PEN at 43° C. is preferably below 350. If one desires to achieve both an increase in softening point according to EN1427 and a reduction in Fraass temperature, the PEN at 43° C. is preferably between 5 and 70, more preferably between 7 and 70. The TBC-GLC recovery at 450° C. is preferably less than 2 wt %, more preferably less than 1 wt %. The softness of the wax can be influenced by adjusting the process conditions of the manufacturing process and/or by blending soft wax and hard wax, wherein the hard wax can be a more normal paraffinic wax such as for example SASOBIT or the Sarawax SX100 or Sarawax SX105 type wax products as obtainable from Shell MDS Malaysia Sdn Bhd.
- Suitable bitumens include those with penetrations in the range of 1 to 450 mm/10 as determined in accordance with EN 1426. The softening point of suitable bitumens may range from 30 to 130° C., preferably, 40 to 100° C. as determined in accordance with EN 1427. The penetration index of suitable bitumens may range between +9 and −3. The viscosity at 60° C. may be 10 to 20,000 Pas.
- The content of soft paraffin wax additive in the bitumen composition according to the invention may be up to 20 wt %, more preferably between 0.1 to 20 wt %, even more preferably between 0.5 to 10 wt %. When the partly isomerized paraffin wax is used, the Fraass temperature decreases, even at higher contents of said partly isomerized paraffin wax. When the substantially normal paraffin wax, like for example the commercial SASOBIT product, is used in a high content, the Fraass temperature does not improve with respect to the starting bitumen.
- The soft paraffin wax additive may be blended with the bitumen using any suitable method. For instance, the additive may be added in divided form, for example as pellets or as a powder or in a molten state, to the bitumen. The bitumen may be in the molten state, which is at a temperature sufficient to dissolve or disperse the additive. Suitable temperatures range between 120 and 230° C., preferably, 130 and 190° C.
- It may be possible to add sufficient additive to the bitumen to produce a wax/bitumen blend of the desired final concentration. In certain applications, however, it may be desirable to produce a concentrated blend or “masterbatch” of the additive and bitumen, which may be mixed with additive-free bitumens or bitumen having a low additive concentration to produce blends of the desired final composition. Suitably, the masterbatch may comprise the additive in a concentration of 10 to 30 wt %.
- The bitumen composition according to the invention may be employed as a binder for aggregates to form an asphalt composition. The aggregates employed in such compositions include conventional aggregates such as granite. Optionally, fillers of, for example, limestone and cellulose may also be included in the bituminous composition. Sand and dust may also be present.
- Other additives may also be present with the soft paraffin wax additive. Examples of possible other additives are polymers such as elastomers, for example styrene-butadiene co-polymer, styrene-butadiene-styrene copolymer; plastomers, for example ethylene vinyl acetate co-polymer, poly ethylene and combinations of said polymers, reactive polymers, for example reactive ethylene ter polymer, acrylate copolymers, cross-linking agents, for example sulphur and sulphur containing compounds, adhesion dopes and IP booster, for example polyphosphoric acid.
- When the bitumen composition according the invention is employed as a binder with aggregates, the bitumen composition may form 1 to 20 wt %, preferably, 2 to 15 wt %, more preferably, 4 to 10 wt %, and most preferably, 4 to 7 wt % of the overall asphalt composition. The aggregate content of the overall composition may be more than 50 wt %, preferably, more than 60 wt %, even more preferably, more than 70 wt % for example, 75 to 90 wt %. The remainder of the asphalt composition may comprise sand, cellulose and/or limestone.
- When preparing the asphalt composition, it may be possible to add the soft paraffin wax additive to the bitumen, in the presence of the aggregates and/or fillers. It may also be possible to mix the additive with the bitumen prior to the addition of aggregate and/or filler. An example of a possible method of adding the soft paraffin wax additive is described in AU-B-200137219.
- Asphalt compositions as described above may be used as pavings and coverings for a variety of surfaces, particularly, for example, lorry parks, motorway road surfacing, air fields, residential roads, service station forecourts, car parks, taxi-ways and driveways. The bitumen composition may also be beneficially used in so-called top layers and sub layers as accordance with the teaching of U.S. Pat. No. 6,588,974 for normal paraffin wax containing bitumen compositions, which reference is incorporated by reference.
- The bitumen composition according to the present invention may also be used as part of so-called joint sealants, which are for example used to fix concrete elements in airport surfaces, or as part of a roofing felt composition.
- The soft paraffin wax additive is preferably obtained by hydroisomerization of the substantially linear paraffin wax as obtained in a Fischer-Tropsch process. The wax having the required congealing point may be isolated by distillation from the hydroisomerized product or alternatively the feed to the hydroisomerization is so chosen that the soft wax additive is directly obtained from the hydroisomerized product. The properties of the wax additive as obtained in said hydroisomerization can be suitably modified by blending the wax as obtained by said hydroisomerization and FT paraffin comprising more than 90% n-alkanes. Examples of the latter are the afore mentioned SASOBIT, Paraflint H1 and Sarawax SX100 and Sarawax SX105. Paraflint H1 is obtainable from Sasol-Moore and Munger. The Sarawax products are obtainable from Shell MDS Malaysia Sdn Bhd. Applicants found that by using a blend of the FT normal paraffin and the soft paraffin wax additive,a bitumen composition can be obtained wherein the Fraass temperature is lowered and the high temperature properties are improved. Preferably the congealing point and the PEN at 43° C. of such a blended wax has the properties as described above.
- Examples of the Fischer-Tropsch synthesis and routes to this soft wax additive are described in WO-A-02102941, EP-A-1498469, WO-A-2004009739 and EP-A-1268712.
- Applicants found that a very suitable soft paraffin wax can be obtained as a by-product of the following process wherein middle distillates are prepared from a Fischer-Tropsch wax. This process comprises the steps of (a) hydrocracking/hydroisomerisating a Fischer-Tropsch product, (b) performing one or more distillate separations on the effluent of step (a) to obtain a middle distillate fuel fraction and a soft paraffin wax additive having an initial boiling point of between 500 and 600° C. The additive is preferably obtained as a residual fraction in a vacuum distillation step. The PEN value at 43° C. of the wax as obtained by this process may be reduced if required by blending this wax with a wax fraction isolated by distillation from the starting Fischer-Tropsch product. This fraction, preferably hydrogenated in order to remove oxygenates and olefins and having a congealing point of between 90 and 120° C., is a substantially normal paraffin wax having a lower PEN value at 43° C. By blending this component with the softer wax a controlled value for the PEN at 43° C. may be obtained.
- In order to obtain a wax additive product having the desired PEN and congealing point in combination with a commercially attractive yield of the middle distillate main product it has been found that it is advantageous to start from a relatively heavy Fischer-Tropsch product. The relatively heavy Fischer-Tropsch product has suitably at least 30 wt %, preferably at least 50 wt %, and more preferably at least 55 wt % of compounds having at least 30 carbon atoms. Furthermore the weight ratio of compounds having at least 60 or more carbon atoms and compounds having at least 30 carbon atoms of the Fischer-Tropsch product is suitably at least 0.2, preferably at least 0.4 and more preferably at least 0.55. Preferably the Fischer-Tropsch product comprises a C20+ fraction having an ASF-alpha value (Anderson-Schulz-Flory chain growth factor) of at least 0.925, preferably at least 0.935, more preferably at least 0.945, even more preferably at least 0.955.
- The initial boiling point of the Fischer-Tropsch product as feed to step (a) may range up to 400° C., but is preferably below 200° C. Preferably any compounds having 4 or less carbon atoms and any compounds having a boiling point in that range are separated from a Fischer-Tropsch synthesis product before the Fischer-Tropsch synthesis product is used in step (a). In addition to the Fischer-Tropsch product, other fractions may be processed in step (a). Possible other fractions may suitably be any excess microcrystalline wax as obtained in step (b).
- Such a Fischer-Tropsch product can be obtained by any process, which yields a relatively heavy Fischer-Tropsch product. Not all Fischer-Tropsch processes yield such a heavy product. An example of a suitable Fischer-Tropsch process is described in WO-A-9934917. These processes may yield a Fischer-Tropsch product as described above.
- The Fischer-Tropsch product will contain no or very little sulphur and nitrogen containing compounds. This is typical for a product derived from a Fischer-Tropsch reaction, which uses synthesis gas containing almost no impurities. Sulphur and nitrogen levels will generally be below the detection limits, which are currently 5 ppm for sulphur and 1 ppm for nitrogen. The soft paraffin wax additive will consequently also have such low sulphur and nitrogen levels. The process conditions and other directions of how to perform the above process have been reported earlier by applicant in WO-A-2004009739 which publication is hereby incorporated by reference.
- The soft wax as obtained from one of the above Fischer-Tropsch processes is suitably transformed into a form in which handling of the product is facilitated. Suitable forms are containers filled with solid wax product, which containers can be heated at the location of use and wherein the wax is added to the bitumen in its liquid state. Heated containers containing the wax in its liquid state may also be used. The wax may also be provided as pellets, extrudates, flakes or powder. In order to prevent the wax particles from sticking to each other, silica powder and the like may be added to provide a less sticky surface of the wax particles.
- The invention will be illustrated with the following non-limiting examples.
- To a 35/50 pen grade bitumen having the properties as listed in Table 2, 1.5, 3 and 6 wt % of a soft paraffin wax additive having the properties as listed in Table 1 have been added. Mixing was performed at 160° C. The soft paraffin wax was made according to the principles of Example 1 of WO-A-2004/009739.
- The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 3.
- Example 1 was repeated using a 70/100 pen grade bitumen having the properties listed in Table 2. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 4.
- Example 1 was repeated using SASOBIT having the properties as listed in Table 1. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 3.
- Example 2 was repeated using SASOBIT having the properties as listed in Table 1. The viscosity at 135, 150 and 170° C. and the Fraass point of the resulting mixtures were measured. The results are listed in Table 4.
- To the 35/50 pen grade bitumen of Example 16 wt % of a 50/50 wt % blend of the soft wax additive and the SASOBIT (see Table 1) were added. The PEN at 43° C. (0.1 mm) of the resulting wax blend was 39.
- The increase in softening point relative to the starting bitumen was 24.6° C. and the decrease in Fraass temperature relative to the starting bitumen was 2° C.
- Table 3 and Table 4 show that at a given concentration and for a given bitumen, the additive of the invention leads to the lowest Fraass breaking point values for the corresponding bituminous blend when compared to the unmodified and the SASOBIT modified bitumen.
- These Tables also show that the additive of the invention reduces the viscosity at a given temperature of the corresponding bitumen blends when compared to the un-modified bitumen.
TABLE 1 Soft paraffin SASOBIT wax additive Congealing point (ISO 2207) (° C.) 100 97 Initial boiling point (° C.) TBC-GLC 470 434 TBC-GLC recovery at 450° C. (wt %) 0 0.6 TBC-GLC recovery at 500° C. (wt %) 1.1 1 PEN at 43° C. (0.1 mm) 3 >250 (*)
(*) the PEN at 43° C. (0.1 mm) for similar soft wax products obtainable via the same process was 317 as expressed in 0.1 mm.
-
TABLE 2 Bitumen PEN at 25° C. Softening point properties (dmm) (EN1426) (° C.) (EN1427) PI (pen25/sft) 35/50 pen grade 41 52 −1.15 70/100 pen grade 84 46.4 −0.87 -
TABLE 3 Additive Viscosity Viscosity Viscosity content at 135° C. at 150° C. at 170° C. Fraass (wt %) (Pa · s) (Pa · s) (Pa · s) (° C.) Bitumen of 0 0.43 0.22 0.10 −7 Example 1 and A Example 1 1.5 0.4 0.2 0.09 −13 A 1.5 0.39 0.2 0.09 −7 Example 1 3 0.35 0.18 0.08 −11 A 3 0.36 0.18 0.08 −7 Example 1 6 0.29 0.15 0.07 −15 A 6 0.22 0.12 0.06 −6 -
TABLE 4 Additive Viscosity Viscosity Viscosity content at 135° C. at 150° C. at 170° C. Fraass (wt %) (Pa · s) (Pa · s) (Pa · s) (° C.) Bitumen of 0 0.25 0.13 0.06 −15 Example 2 and B Example 2 1.5 0.24 0.13 0.06 −19 B 1.5 0.24 0.12 0.06 −12 Example 2 3 0.22 0.11 0.05 −16 B 3 0.21 0.11 0.05 −10 Example 2 6 0.18 0.1 0.05 −25 B 6 0.17 0.1 0.05 −10
Claims (19)
1. A bitumen composition comprising a paraffin wax, wherein the wax has a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
2. A bitumen composition according to claim 1 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of more than 7.
3. A bitumen composition according to claim 1 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of below 350.
4. A bitumen composition according to claim 3 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of below 70.
5. A bitumen composition according to claim 1 , wherein the bitumen component has a penetration in the range of 1 to 450 mm/10, a softening point from 30 to 130° C., a penetration index between +9 and −3 and a viscosity at 60° C. between 10 to 20,000 Pas.
6. A bitumen composition according to claim 1 , wherein the content of the paraffin wax is between 0.5 and 10 wt %.
7. A bitumen composition according to claim 1 , wherein the paraffin wax is obtained by a process comprising the steps of (a) hydrocracking/hydroisomerisating a Fischer-Tropsch product, (b) performing one or more distillate separations on the effluent of step (a) to obtain a middle distillate fuel fraction and a soft paraffin wax additive having an initial boiling point of between 500 and 600° C.
8. A bitumen composition according to claim 7 wherein the wax as obtained in said process is blended with a normal paraffin wax fraction having a congealing point of between 90 and 120° C. as isolated by distillation from the Fischer-Tropsch product.
9. An asphalt composition comprising aggregates and between 1 and 20 wt % of the bitumen composition according to claim 1 .
10. An asphalt composition according to claim 9 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of more than 7.
11. An asphalt composition according to claim 9 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of below 350.
12. An asphalt composition according to claim 11 , wherein the paraffin wax has a PEN at 43° C. as determined by IP 376 of below 70.
13. An asphalt composition according to claim 9 , wherein the bitumen component has a penetration in the range of 1 to 450 mm/10, a softening point from 30 to 130° C., a penetration index between +9 and −3 and a viscosity at 60° C. between 10 to 20,000 Pas.
14. An asphalt composition according to claim 9 , wherein the content of the paraffin wax is between 0.5 and 10 wt %.
15. An asphalt composition according to claim 9 , wherein the paraffin wax is obtained by a process comprising the steps of (a) hydrocracking/hydroisomerisating a Fischer-Tropsch product, (b) performing one or more distillate separations on the effluent of step (a) to obtain a middle distillate fuel fraction and a soft paraffin wax additive having an initial boiling point of between 500 and 600° C.
16. An asphalt composition according to claim 15 wherein the wax as obtained in said process is blended with a normal paraffin wax fraction having a congealing point of between 90 and 120° C. as isolated by distillation from the Fischer-Tropsch product.
17. A road surface comprising the asphalt composition of claim 9 .
18. A paraffin wax having a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5 in suitable form for use as a bitumen additive.
19. A process to lower the Fraass point of a bitumen composition comprising adding to a bitumen composition a paraffin wax having a congealing point of between 85 and 120° C. and a PEN at 43° C., expressed in 0.1 mm, as determined by IP 376 of more than 5.
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EP05292400 | 2005-11-10 |
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US11/558,711 Abandoned US20070199476A1 (en) | 2005-11-10 | 2006-11-10 | Bitumen composition |
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US (2) | US8003717B2 (en) |
EP (2) | EP1951818B1 (en) |
JP (2) | JP5172689B2 (en) |
KR (1) | KR101313642B1 (en) |
CN (1) | CN101305053B (en) |
AT (2) | ATE432323T1 (en) |
AU (1) | AU2006311065B2 (en) |
BR (1) | BRPI0618644A2 (en) |
CA (1) | CA2628679A1 (en) |
DE (2) | DE602006005396D1 (en) |
NO (1) | NO20082577L (en) |
RU (1) | RU2008123537A (en) |
WO (2) | WO2007054541A1 (en) |
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US20100227954A1 (en) * | 2009-03-08 | 2010-09-09 | Asphalt & Wax Innovations, LLC. | Asphalt modifiers, methods of modifying asphalt, asphalt compositions and methods of making |
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US8088845B2 (en) | 2007-05-10 | 2012-01-03 | Shell Oil Company | Paraffin wax composition |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030002920A1 (en) * | 1997-08-29 | 2003-01-02 | Gunter Hildebrand | Bitumen or asphalt for producing a road topping, road topping and method for the production of bitument or asphalt |
US20040102547A1 (en) * | 2000-08-25 | 2004-05-27 | Cowley Lloyd Graham | Use of a bitumen/wax composition |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1232791A (en) * | 1968-02-08 | 1971-05-19 | ||
US3655563A (en) * | 1970-04-20 | 1972-04-11 | Atlantic Richfield Co | Lubricating composition |
ZA772579B (en) * | 1977-04-29 | 1979-01-31 | Gypsum Ind Ltd | Improvements relating to gypsum products |
DE3509037A1 (en) | 1985-03-14 | 1986-09-18 | Hüls AG, 4370 Marl | COVERING MEASUREMENT FOR A POLYMER-MODIFIED ROOF AND SEALING SHEET |
DE19838770C2 (en) * | 1997-08-29 | 2002-10-24 | Schuemann Sasol Gmbh & Co Kg | Bitumen, roofing felt with bitumen and use of FT paraffin |
KR100590415B1 (en) | 1997-12-30 | 2006-06-19 | 쉘 인터내셔날 리서치 마챠피즈 비.브이. | Fischer-Tropsch catalyst based on cobalt |
JP3311299B2 (en) * | 1998-10-21 | 2002-08-05 | 南己 伊藤 | Asphalt modifier and asphalt composition containing the same |
US6776898B1 (en) | 2000-04-04 | 2004-08-17 | Exxonmobil Research And Engineering Company | Process for softening fischer-tropsch wax with mild hydrotreating |
WO2002102941A2 (en) | 2001-06-15 | 2002-12-27 | Shell Internationale Research Maatschappij B.V. | Process for preparing a microcrystalline wax |
US7300565B2 (en) * | 2002-07-18 | 2007-11-27 | Shell Oil Company | Process to prepare a microcrystalline wax and a middle distillate fuel |
JP2004315826A (en) * | 2004-05-21 | 2004-11-11 | Tajima Roofing Co Ltd | Modified asphalt for thermal construction at low temperature |
-
2006
- 2006-11-09 JP JP2008539425A patent/JP5172689B2/en not_active Expired - Fee Related
- 2006-11-09 EP EP06829949A patent/EP1951818B1/en not_active Not-in-force
- 2006-11-09 DE DE602006005396T patent/DE602006005396D1/en active Active
- 2006-11-09 KR KR1020087013371A patent/KR101313642B1/en not_active Expired - Fee Related
- 2006-11-09 DE DE602006007032T patent/DE602006007032D1/en active Active
- 2006-11-09 WO PCT/EP2006/068298 patent/WO2007054541A1/en active Application Filing
- 2006-11-09 JP JP2008539436A patent/JP5167139B2/en not_active Expired - Fee Related
- 2006-11-09 CA CA002628679A patent/CA2628679A1/en not_active Abandoned
- 2006-11-09 US US12/093,073 patent/US8003717B2/en not_active Expired - Fee Related
- 2006-11-09 AT AT06829949T patent/ATE432323T1/en not_active IP Right Cessation
- 2006-11-09 BR BRPI0618644A patent/BRPI0618644A2/en not_active IP Right Cessation
- 2006-11-09 EP EP06807794A patent/EP1957586B1/en not_active Not-in-force
- 2006-11-09 CN CN2006800418904A patent/CN101305053B/en not_active Expired - Fee Related
- 2006-11-09 WO PCT/EP2006/068201 patent/WO2007054503A1/en active Application Filing
- 2006-11-09 AT AT06807794T patent/ATE423820T1/en not_active IP Right Cessation
- 2006-11-09 RU RU2008123537/04A patent/RU2008123537A/en not_active Application Discontinuation
- 2006-11-09 AU AU2006311065A patent/AU2006311065B2/en not_active Ceased
- 2006-11-10 US US11/558,711 patent/US20070199476A1/en not_active Abandoned
-
2008
- 2008-04-07 ZA ZA200803012A patent/ZA200803012B/en unknown
- 2008-06-09 NO NO20082577A patent/NO20082577L/en not_active Application Discontinuation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030002920A1 (en) * | 1997-08-29 | 2003-01-02 | Gunter Hildebrand | Bitumen or asphalt for producing a road topping, road topping and method for the production of bitument or asphalt |
US20040102547A1 (en) * | 2000-08-25 | 2004-05-27 | Cowley Lloyd Graham | Use of a bitumen/wax composition |
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AU2008250263B2 (en) * | 2007-05-10 | 2012-06-07 | Shell Internationale Research Maatschappij B.V. | Paraffin wax composition |
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CN114933810A (en) * | 2022-04-28 | 2022-08-23 | 宁夏鑫睿途道路工程技术有限公司 | Warm-mixed asphalt mixture and preparation method thereof |
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KR20080072035A (en) | 2008-08-05 |
ATE423820T1 (en) | 2009-03-15 |
WO2007054541A1 (en) | 2007-05-18 |
RU2008123537A (en) | 2009-12-20 |
JP5167139B2 (en) | 2013-03-21 |
US8003717B2 (en) | 2011-08-23 |
DE602006007032D1 (en) | 2009-07-09 |
US20080255277A1 (en) | 2008-10-16 |
JP2009516095A (en) | 2009-04-16 |
EP1951818A1 (en) | 2008-08-06 |
DE602006005396D1 (en) | 2009-04-09 |
CN101305053A (en) | 2008-11-12 |
CA2628679A1 (en) | 2007-05-18 |
CN101305053B (en) | 2013-03-27 |
BRPI0618644A2 (en) | 2016-11-22 |
JP5172689B2 (en) | 2013-03-27 |
NO20082577L (en) | 2008-06-09 |
EP1957586B1 (en) | 2009-02-25 |
AU2006311065A1 (en) | 2007-05-18 |
EP1951818B1 (en) | 2009-05-27 |
ATE432323T1 (en) | 2009-06-15 |
KR101313642B1 (en) | 2013-10-02 |
WO2007054503A1 (en) | 2007-05-18 |
EP1957586A1 (en) | 2008-08-20 |
ZA200803012B (en) | 2009-02-25 |
AU2006311065B2 (en) | 2010-06-10 |
JP2009516013A (en) | 2009-04-16 |
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