GB2036785A - Utilizing Pyrolysis Oil from a Scrap-Rubber Pyrolysis - Google Patents
Utilizing Pyrolysis Oil from a Scrap-Rubber Pyrolysis Download PDFInfo
- Publication number
- GB2036785A GB2036785A GB7923879A GB7923879A GB2036785A GB 2036785 A GB2036785 A GB 2036785A GB 7923879 A GB7923879 A GB 7923879A GB 7923879 A GB7923879 A GB 7923879A GB 2036785 A GB2036785 A GB 2036785A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oil
- pyrolysis
- scrap
- rubber
- bitumen
- 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.)
- Granted
Links
- 238000000197 pyrolysis Methods 0.000 title claims abstract description 16
- 229920001971 elastomer Polymers 0.000 title claims abstract description 8
- 239000005060 rubber Substances 0.000 title claims abstract description 8
- 238000009835 boiling Methods 0.000 claims abstract description 20
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- 239000010426 asphalt Substances 0.000 abstract description 15
- 229920003048 styrene butadiene rubber Polymers 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 27
- 239000004033 plastic Substances 0.000 description 6
- 230000009467 reduction Effects 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000010920 waste tyre Substances 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- NNYBQONXHNTVIJ-UHFFFAOYSA-N etodolac Chemical compound C1COC(CC)(CC(O)=O)C2=C1C(C=CC=C1CC)=C1N2 NNYBQONXHNTVIJ-UHFFFAOYSA-N 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229940063718 lodine Drugs 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- -1 poly propylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
- C10C3/00—Working-up pitch, asphalt, bitumen
- C10C3/005—Working-up pitch, asphalt, bitumen by mixing several fractions (also coaltar fractions with petroleum fractions)
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Working-Up Tar And Pitch (AREA)
Abstract
The oil resulting from scrap-rubber pyrolysis, and boiling above 160 DEG C, is added to bituminous compounds. The boiling point must be above the manufacturing temperature of bitumen, which fluctuates between 160 DEG C and 200 DEG C. Other synthetic materials (e.g. styrene-butadiene copolymer) may be dissolved in the oil before mixing it with bituminous compounds.
Description
SPECIFICATION
Process for Utilizing Pyrolysis Oil From a Scrap-rubber Pyrolysis, especially of Scrap-tires
Object of the invention is a bituminous mass, in case containing synthetic material and a process
of its manufacture. The winning of the pyrolysis oil used in the bituminous mass was carried out by
means of dry distillation at a temperature of 4000C--8000C, which is comperable to the processes
described, for example, in DT-OS 25 20 774 or DT-AS 2404 800.
According to the present state of technology only suggestions had been made to utilize pyrolysis
oil as a crude oil substitute or fractionated in light and heavy oil (IT-PS 3 28 776), as fuel or for heating
purposes (DE-PS 635 098). The utilizing possibilities are, however, unsatisfactory since the pyrolysis
oils contain too high a content of sulphur according to the present regulations and are also adulterated by other substances (for example 02, N2). This especially concerns the higher boiling portions of the
pyrolysis oil. Furthermore, there is a risk of gumming-up since the oils are highly unsaturated.
All these disadvantages can only be remedied by means of expensive refining. It is true, that with this process, low boiling portions of pyroloysis oil can be regenerated to various products of greater value (solvents, resin raw materials etc.). However, for the higher boiling portions, according to the present state of technology, such a regeneration to products of higher value has hitherto been
unknown (GB-PS 1 471 038).
Thus the problem arises of applying a fraction gained via the scrap-rubber pyrolysis, to a new
purposes, and which should boil preferably above 1600C.
The solution to the problem consists in a bituminous mass in case containing synthetic material, characterized by a content of pyrolysis oil fraction from scrap-rubber and boiling above 1 600C. In any case, the boiling point of the pyrolysis oil fraction must be above the manufacturing temperature of the bitumen, which fluctuates between 1 6000 and 2000C depending on the kind of bitumen and additives utilized, in order to prevent a distilling-off of low-boiling portions.
The bituminous mass containing synthetic material is produced by imbibing or dissolving synthetic materials in a pyrolyses oil fraction boiling above 1 6000 gained from scrap-rubber before mixing it with the bituminous compound.
The pyrolysis oil (from scrap-tires) used in Example 1-4 was carried out by distillation at a temperature of 4000C--8000C in absence of oxygen and a slow rise of temperature. The oil is characterized as follows:
Fraction lodine test Fraction
boiling (acc. to boiling
above 200 OC Hants) above 1600C
Density at 200C 0.94 g/cm3 0.2 g of Oil 0.93 g/cm3
Content of sul- 1.32% duration:1h 1.24%
phur (acc. to
Schoeninger)
Boiling-progress: % % 1600C--1800C - 95 9.8 1800C--2000C - 86 9.9 2000C--2250C 6.0 86 4.8 2250C--2500C 11.4 75 9.2 2500C--3000C 12.4 56 9.9 300 C350 C 31.6 55 25.3 3500C--3800C 31.6 48 25.3
rest 7.1 5.7
The utilization of this fraction has decisive advantages for processing bituminous compounds such as for example roof and sealing widths sound and heat-insulating boards, permanently elastic joint sealing and putty compounds, bitumen plastic widths, plastic widths, self-adhesive widths, selfadhesive sealing widths.
The advantages referred to in the following examples are especially concerned with:
1. Reduction of the breaking point
2. Oxidation reduction of the bitumen
3. Increase of elasticity
4. Increase of tensibility
5. Increase of ductility
6. Increase of adhesive power
7. Reduction of hardness
8. Improvement of the solubility for synthetic materials used in bitumen
9.Decrease of the agitating periods
Example 1
Reduction of Breaking Point (Example of a Mixture for Roof and Sealing Widths)
Breaking point
after an agitating
period of 24 hrs
Breaking point at 160 0C B100/40 100% -130C -30C
(without oil)
B100/40 85% -190C -120C Oil (boiling 15% point above 2000C)
8100/40 85% -200C -140C Oil (boiling 15% point above 1 600C) The relatively unsaturated character of the oil achieves a reduction in the oxidation of the bitumen, which is shown in a substantial change in the breaking points of the specimens.
Example 2
Ductility, Tensibility, Elasticity, Hardness (Example of a Mixture for a Plastic Width Containing
50% or More Synthetic Material, Especially a Self-adhesive Plastic Width)
ductility at 25 0C hardness elasticity
DIN 1995 Tensibility (at 22 OCJ (at 22 C) material in cm % DIN 53504 DIN 53505 DIN 53512
I. Atactic poly
propylene (APP) 50% / B 25* 50% 5 61 39 9 II. APP 50% / B 25* 25% 6 91 18 11
Oil 25% (boiling point above 2000C) *see DIN 1995
When adding oil the adhesive power is also increased.
When mixing synthetic materials into the bitumen further advantages can be achieved in accordance with the invention. The oil improves the dissolving of the synthetic material in the bitumen and in this way reduces the agitating periods considerably.
Example 3
Agitating Periods at 1 600C (Example of a Bitumen Plastic Width)
Styrol-butadien- (17.65%) 1 5 portions 3 hrs 35 mins
copolymerisate
B 25 (87.35%) 70 portions
Styrol-butadien- 15%
copolymerisate
B 25 70% 2 hrs 5 mins Oil (boiling point 15% above 2000 C) Styrol-butadien- 15% copolymerisate B25 70% 2 hrs 12 mins
Oil (boiling point 15% above 1600C)
Furthermore, it is possible, according to the process of the invention to imbibe or dissolve the synthetic materials in oil and then mix these solutions into the bitumen. As a result of this process a further considerable reduction of the agitating periods is achieved.
Example 4
Agitating Periods at 1 600C (Example of a Bitumen Plastic Width)
Synthetic Material Synthetic material
Material only mixed with oil previously dissolved
in oil
Styrol-butadien- 15%
copolymerisate
B 25 70% 2 hrs 5 mins 5 mins
Oil (boiling point 15% above 20O0C) Styrol-butadien- 15%
copolymerisate
B 25 70% 2 hrs 12 mins 6 mins
Oil (boiling point 15% above 1600C) To dissolve the synthetic materials e.g. styrol-butadien-copolymerisate can be achieved at 1 600C and then this process lasts 1 5 mins.
The solution thus obtained can be mixed into bitumen without any substantial loss of heat when being used immediately. Owing to this process not only the costs are reduced on account of the decrease of the agitating period, but also the oxidation of the bituminous compounds.
A further substantial advantage is that these synthetic solutions can be mixed into distilled bitumens, but also into blown bitumen, without reducing the quality. Furthermore, synthetic materials can be used such as synthetic caoutchouc, which are only rarely utilized in blown bitumen because of their bad solubility, for example.
Claims (2)
1. Bituminous in case synthetic materials containing compounds characterized by a content of a pyrolysis oil fraction obtained from scrap-rubber and boiling above 1 600 C.
2. Process of manufacturing a bituminous compound containing synthetic material characterized by the fact that the synthetic material is imbibed or dissolved in a pyrolysis oil fraction boiling above 1 600C which is obtained from scrap-rubber before mixing it into the bituminous compound.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7831262 | 1978-07-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2036785A true GB2036785A (en) | 1980-07-02 |
| GB2036785B GB2036785B (en) | 1983-05-11 |
Family
ID=10498691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7923879A Expired GB2036785B (en) | 1978-07-14 | 1979-07-09 | Utilizing pyrolysis oil from a scrap-rubber pyrolysis |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2036785B (en) |
-
1979
- 1979-07-09 GB GB7923879A patent/GB2036785B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2036785B (en) | 1983-05-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |