CA2346022A1 - Method for treatment of vulcanized rubber - Google Patents
Method for treatment of vulcanized rubber Download PDFInfo
- Publication number
- CA2346022A1 CA2346022A1 CA 2346022 CA2346022A CA2346022A1 CA 2346022 A1 CA2346022 A1 CA 2346022A1 CA 2346022 CA2346022 CA 2346022 CA 2346022 A CA2346022 A CA 2346022A CA 2346022 A1 CA2346022 A1 CA 2346022A1
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- Prior art keywords
- solution
- rubber
- blend
- sulfur
- fatty acid
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/18—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material
- C08J11/22—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds
- C08J11/26—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with organic material by treatment with organic oxygen-containing compounds containing carboxylic acid groups, their anhydrides or esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J11/00—Recovery or working-up of waste materials
- C08J11/04—Recovery or working-up of waste materials of polymers
- C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
- C08J11/16—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by treatment with inorganic material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Abstract
According to the present invention there is provided a method for the treatment of vulcanized rubber comprising the steps of: providing a solution of sulfur in a fatty acid or ester or a salt thereof; blending the solution with particulate vulcanized rubber; and heating the blend for a time period and at a sufficient temperature and pressure to substantially devulcanize the rubber.
Description
METHOD FOR TREATMENT OF VULCANIZED RUBBER
The present invention relates to a method for the treatment of vulcanized rubber, in particular waste rubber, and a chemical solution for use in such a treatment method. In particular, the invention relates to a method for reclaiming waste rubber such as rubber crumb from used tyres, tyre tubing, hosing or other scrap, by dewlcanization.
Sulfur wlcanization of a rubber polymer is a chemical process which forms a three dimensional network by interconnecting polymer chains, such as through sulfur atoms.
Various other wlcanization systems are also possible including processes where the cross-linking entity is a carbon-carbon bond, a divalent organic radical, or a polyvalent metal.
These processes produce wlcanized rubber having increased elasticity and decreased plasticity. In this regard, wlcanizf:d rubber generally retracts forcibly to its moulded shape after being deformed by some typE; of mechanical force.
The ever increasing cost of crude natural rubber, primarily due to its scarcity, has made the recycling or reclaiming of waste rubber economically attractive for many years. For example, several acid processes :for reclaiming rubber are known. Such processes are typically applicable to the treatment of waste rubber having a relatively low state of wlcanization and containing no free sulfur. These processes are, however, generally not suitable for more highly wlcauized rubber such as hose, belting and tyre scrap.
Furthermore, rubber which has been reclaimed by acid processes usually disadvantageously contains small traces of acid which causes rapid deterioration of the rubber.
The tensile strength and other physical properties of acid reclaimed rubber are generally poor.
Alkali processes for reclaiming rubber are also known and are generally considered to provide .some advantages over the above mentioned acid processes. However, sulfur contained in the waste rubber is not removed by alkali processes, but rather the bonding between the sulfur and the rubber is altered. Disadvantageously, after scrap wlcanized rubber has been reclaimed through an alkali process, it typically loses toughness and elasticity, and generally becomes susceptible to plastic deformation.
The present invention aims to provide an alternative method for the treatment and reclaiming of vulcanized rubber and solutions for use in such a method.
According to one aspect of the present invention there is provided a method for the treatment of vulcanized rubber comprising the steps of:
providing a treatment solution of sulfur in a fatty acid or ester or a salt thereof;
blending the solution with particulate vulcanized rubber; and heating the blend for a tinne period and at a sufficient temperature and pressure to substantially devulcanize the rubber.
Preferably an oil-base softening agent is added to the blend prior to heating of the blend to soften the rubber during treatment. The addition of softening agent is particularly preferred if the rubber being treated is dry. On the other hand, if the rubber is relatively fresh scrap, the softening agent may not be required. An appropriate amount of softening agent may generally be determined empirically from the nature of the rubber.
Duting blending of the vulcanized rubber with the solution and optionally the softening agent, it is preferred that the mixing vessel be cooled, for example by water cooling. Cooling of the blend advantageously ensures that the blend does not become sticky and, therefore, unable to be thoroughly blended.
The blend may be heated for any suitable time period depending on, for example, the degree of vulcanization of the rubber being treated and/or the particle size of the particulate rubber.
However, the blend is typically heated for a time period of from about 1 hour to about 8 hours, preferably from about 4 hours to about 8 hours.
The temperature at which the blend is heated is advantageously chosen to avoid burning of the rubber being treated. In this regard, the blend is preferably heated at a temperature of from about 180°C to about 200'°C. Similarly, the pressure at which the treatment is conducted may be determined based on the degree of vulcanization of the rubber and depending on the selected time period and temperature of treatment. In a preferred embodiment, the treatment is carried out at a pressure of from about 18 to about 20 kg/cm2.
The amounts of the constituents; of the blend will generally depend on the particular characteristics of the rubber to be treated. For example, the amount of solution of sulfur and fatty acid or ester or salt thereof may vary depending on the degree of vulcanization of the rubber. In a preferred embodiment the blend comprise about 100 parts particulate rubber, 4 to 6 parts softening agent and 2 to 4 parts treatment solution.
The particulate rubber may be of any suitable particle size. Generally, the smaller the particle size the more effective and efficient the reaction. In a preferred embodiment the 1 S rubber is rubber crumb having a p;~rticle size of less than 6mm. Most preferably the rubber is powdered rubber.
The solution of sulfur and fatty acid or ester or salt thereof preferably comprises a solution of sulfur and fatty acid or ester or ;salt thereof in a ratio of 1:4. However, the concentration of sulfur in the solution may vary depending on the degree of vulcanization of the rubber.
In a preferred embodiment, the fatity acid or ester or salt thereof is an unsaturated fatty acid or ester or salt thereof. More preferably the fatty acid is oleic acid.
The solution is preferably prepared. by adding powdered ventilated sulfur to oleic acid which has been heated to approximately 160°C while stirring the solution.
After the addition of the sulfur, typically in a ratio of suifiir to oleic acid of 1:4, the temperature of the solution is increased until the sulfur is completely dissolved in the oleic acid.
Generally, it has been found that a temperature of 180~'C is sufficient to dissolve the sulfur in the oleic acid.
Alternatively, the sulfur may be added to cold oleic acid, and the solution subsequently heated to dissolve the sulfur.
Accordingly, the invention also provides a solution for treating vulcanized rubber, the solution comprising:
a fatty acid or ester or a salt thereof; and sulfur.
The oil based softening agent ma.y comprise any suitable softening agent.
However, in a preferred embodiment the softeiung agent is an aromatic oil. For example, in some embodiments a filtered sump oil rnay be used as the oil based softening agent.
The heating of the blend may be achieved by any suitable means. In a preferred embodiment however, heating is achieved in an. autoclave, most preferably a rotating autoclave. Rotation facilitates an even heating of the blend being treated. For example, a "Maxiterm" autoclave has been found appropriate for tr~is purpose. Alternatively, it is envisaged that the entire process or at least a substantial part of the process, may be achieved using a continuous process. In this regard, the treatment process may comprise conveying the material to be treated through a number of treatment stages, each of which carries out a step in the process of the invention.
When heating is conducted in an autoclave the blend is preferably placed in trays having a depth of approximately lOcm. The blend is preferably evenly spread in the tray to a depth of approximately Scm.
Following heating the blend is cooled or allowed to cool. For example, cooling may be effected using a water cooling syst~:m. Once the blend is cooled, it is transferred to a milling station where it is milled, again preferably with water cooling. Most preferably the treated rubber is milled a plurality of times, for example three times.
The milled rubber is preferably tlhen heated, for example in an oven, up to about 130°C.
Following heating, the rubber is once again cooled and remilled. The remilled rubber, which is substantially 100% reclaimed robber, may then be formed into pallets for sale.
The present invention relates to a method for the treatment of vulcanized rubber, in particular waste rubber, and a chemical solution for use in such a treatment method. In particular, the invention relates to a method for reclaiming waste rubber such as rubber crumb from used tyres, tyre tubing, hosing or other scrap, by dewlcanization.
Sulfur wlcanization of a rubber polymer is a chemical process which forms a three dimensional network by interconnecting polymer chains, such as through sulfur atoms.
Various other wlcanization systems are also possible including processes where the cross-linking entity is a carbon-carbon bond, a divalent organic radical, or a polyvalent metal.
These processes produce wlcanized rubber having increased elasticity and decreased plasticity. In this regard, wlcanizf:d rubber generally retracts forcibly to its moulded shape after being deformed by some typE; of mechanical force.
The ever increasing cost of crude natural rubber, primarily due to its scarcity, has made the recycling or reclaiming of waste rubber economically attractive for many years. For example, several acid processes :for reclaiming rubber are known. Such processes are typically applicable to the treatment of waste rubber having a relatively low state of wlcanization and containing no free sulfur. These processes are, however, generally not suitable for more highly wlcauized rubber such as hose, belting and tyre scrap.
Furthermore, rubber which has been reclaimed by acid processes usually disadvantageously contains small traces of acid which causes rapid deterioration of the rubber.
The tensile strength and other physical properties of acid reclaimed rubber are generally poor.
Alkali processes for reclaiming rubber are also known and are generally considered to provide .some advantages over the above mentioned acid processes. However, sulfur contained in the waste rubber is not removed by alkali processes, but rather the bonding between the sulfur and the rubber is altered. Disadvantageously, after scrap wlcanized rubber has been reclaimed through an alkali process, it typically loses toughness and elasticity, and generally becomes susceptible to plastic deformation.
The present invention aims to provide an alternative method for the treatment and reclaiming of vulcanized rubber and solutions for use in such a method.
According to one aspect of the present invention there is provided a method for the treatment of vulcanized rubber comprising the steps of:
providing a treatment solution of sulfur in a fatty acid or ester or a salt thereof;
blending the solution with particulate vulcanized rubber; and heating the blend for a tinne period and at a sufficient temperature and pressure to substantially devulcanize the rubber.
Preferably an oil-base softening agent is added to the blend prior to heating of the blend to soften the rubber during treatment. The addition of softening agent is particularly preferred if the rubber being treated is dry. On the other hand, if the rubber is relatively fresh scrap, the softening agent may not be required. An appropriate amount of softening agent may generally be determined empirically from the nature of the rubber.
Duting blending of the vulcanized rubber with the solution and optionally the softening agent, it is preferred that the mixing vessel be cooled, for example by water cooling. Cooling of the blend advantageously ensures that the blend does not become sticky and, therefore, unable to be thoroughly blended.
The blend may be heated for any suitable time period depending on, for example, the degree of vulcanization of the rubber being treated and/or the particle size of the particulate rubber.
However, the blend is typically heated for a time period of from about 1 hour to about 8 hours, preferably from about 4 hours to about 8 hours.
The temperature at which the blend is heated is advantageously chosen to avoid burning of the rubber being treated. In this regard, the blend is preferably heated at a temperature of from about 180°C to about 200'°C. Similarly, the pressure at which the treatment is conducted may be determined based on the degree of vulcanization of the rubber and depending on the selected time period and temperature of treatment. In a preferred embodiment, the treatment is carried out at a pressure of from about 18 to about 20 kg/cm2.
The amounts of the constituents; of the blend will generally depend on the particular characteristics of the rubber to be treated. For example, the amount of solution of sulfur and fatty acid or ester or salt thereof may vary depending on the degree of vulcanization of the rubber. In a preferred embodiment the blend comprise about 100 parts particulate rubber, 4 to 6 parts softening agent and 2 to 4 parts treatment solution.
The particulate rubber may be of any suitable particle size. Generally, the smaller the particle size the more effective and efficient the reaction. In a preferred embodiment the 1 S rubber is rubber crumb having a p;~rticle size of less than 6mm. Most preferably the rubber is powdered rubber.
The solution of sulfur and fatty acid or ester or salt thereof preferably comprises a solution of sulfur and fatty acid or ester or ;salt thereof in a ratio of 1:4. However, the concentration of sulfur in the solution may vary depending on the degree of vulcanization of the rubber.
In a preferred embodiment, the fatity acid or ester or salt thereof is an unsaturated fatty acid or ester or salt thereof. More preferably the fatty acid is oleic acid.
The solution is preferably prepared. by adding powdered ventilated sulfur to oleic acid which has been heated to approximately 160°C while stirring the solution.
After the addition of the sulfur, typically in a ratio of suifiir to oleic acid of 1:4, the temperature of the solution is increased until the sulfur is completely dissolved in the oleic acid.
Generally, it has been found that a temperature of 180~'C is sufficient to dissolve the sulfur in the oleic acid.
Alternatively, the sulfur may be added to cold oleic acid, and the solution subsequently heated to dissolve the sulfur.
Accordingly, the invention also provides a solution for treating vulcanized rubber, the solution comprising:
a fatty acid or ester or a salt thereof; and sulfur.
The oil based softening agent ma.y comprise any suitable softening agent.
However, in a preferred embodiment the softeiung agent is an aromatic oil. For example, in some embodiments a filtered sump oil rnay be used as the oil based softening agent.
The heating of the blend may be achieved by any suitable means. In a preferred embodiment however, heating is achieved in an. autoclave, most preferably a rotating autoclave. Rotation facilitates an even heating of the blend being treated. For example, a "Maxiterm" autoclave has been found appropriate for tr~is purpose. Alternatively, it is envisaged that the entire process or at least a substantial part of the process, may be achieved using a continuous process. In this regard, the treatment process may comprise conveying the material to be treated through a number of treatment stages, each of which carries out a step in the process of the invention.
When heating is conducted in an autoclave the blend is preferably placed in trays having a depth of approximately lOcm. The blend is preferably evenly spread in the tray to a depth of approximately Scm.
Following heating the blend is cooled or allowed to cool. For example, cooling may be effected using a water cooling syst~:m. Once the blend is cooled, it is transferred to a milling station where it is milled, again preferably with water cooling. Most preferably the treated rubber is milled a plurality of times, for example three times.
The milled rubber is preferably tlhen heated, for example in an oven, up to about 130°C.
Following heating, the rubber is once again cooled and remilled. The remilled rubber, which is substantially 100% reclaimed robber, may then be formed into pallets for sale.
Advantageously, waste rubber treated by the method according to the invention produces reclaimed rubber which may be siimilar to crude rubber and can advantageously be used in the manufacture of rubber articles. Also, the reclaimed rubber may be revulcanized in the normal manner, or it may be mixE;d with synthetic rubber or natural rubber as required.
Preferred embodiments of the present invention will now be described in more detail with reference to the following examples which should not be construed as limiting on the invention in any way.
PrP,~garation of sulfur solution 1000g of oleic acid was introduced to a cold reactor and 250g of powered ventilated sulfur was added thereto with stirring. The reactor was closed with continual mixing of the solution. The solution was then heated to between 160°C and 180°C to completely dissolve the sulfur in the oleic acid. The s~~lution is then allowed to cool.
Throughout the heating process, ~:he solution was periodically checked to see whether the sulfur had dissolved. Generally, the solution was checked at about 150°C, 160°C and 170°C
by placing a drop of the liquid on a glass plate. If the drop was not clear, the sulfur was not completely dissolved. Heating was. continued until a clear and transparent drop was achieved on the glass plate.
Care should be taken when preparing the sulfur solution to evacuate or eliminate any sulfur dioxide gas produced. This may 1>e achieved through an exhaust fan or by using a caustic vapour trap.
1. Rubber Devulcanization Process Car tyre crumb rubber particles and chemical additives were weighed to the specified formulation. The ingredients were well mixed in a rotational mixer. The blend was then placed in layers in a device and heated. The resulting product was then milled on a two roll mill.
For truck tyre crumb rubber particles, the same procedure was followed.
2. Preparation of Rubber Samples The treated rubber was mixed with curatives at three levels, viz Car lyre samp).e:
{a) 50 % dewlcanized rubber and 50 % virgin uncured tyre tread (mainly natural rubber).
(b) 60% dewlcanized rwbber and 40% virgin uncured tyre tread.
{c) 30% dewlcanized »bber and 70% virgin uncured tyre tread.
Truck tyre sample:
(d) 50 % treated rubber and 50 % virgin uncured tyre tread {mainly natural rubber).
(e) 60 % treated rubber and 40 % virgin uncured tyre tread.
(f) 30 % treated rubber and 70 % virgin uncured tyre tread.
The above car and truck tyre samples were processed on a two roll mill and there were no processing difficulties encountered. The treated rubber blended with the virgin tyre stock without difficulties.
The samples were cured under normal curing conditions for truck tyres in a compression press.
3. Sample Evaluation 3.1 $~ecimen Preparation and Conditioning Test specimens were cut to ASTM D412 Die C from cured samples and conditioned at 23 ° C, 50 % humidity for 24 hours .
S
3.2 Testing Conditions Testing machine: LLOYD 20008 with computer interface;
Testing speed: 500 ;mm/min Temperature: 23 °C:
Humidity: 50%
Specimens tested: 3 for each sample 3.3 Test Results The average results are summarised in the following table.
Car T,~~re Sample LD. Tensile Modulus (Mpa)Elongation Hardness at (Devulcanized Strength at 300% Break (%) (Shore A) rubber/tyre (Mpa) Elongation tread stock) (a) (50/50) 4.29 2.57 463.6 56.8 (b) (60/40) 4.74 2.76 489.7 56.4 (c) (30/70) 7.23 2.61 702.4 58.0 Sample LD. Tensile Modulus Elongation Hardness at (DevulcanizedStrength (Mpa) at Break (%) (Shore A) rubber/tyre (Mpa) 300%
tread stock) Elongation (d) (50/50) 6.5 3.0 559.4 59 (e) (60/40) 7.2 3.3 586.1 58 (f) (30/70) 9.8 2.7 803.3 61 _g_ Conclusion The rubber devulcanization process is capable of producing a product that is compatible with rubber compounds. The performsmce of these compounds can be optimised with regard to the cure system, polymer type, filler level, sulfur level and level of addition of the devulcanized material.
The tests conducted show that :including . 30% of devulcanized material derived from passenger tyres into a tread formulation has resulted in a material with useful properties, i.e.
significant tensile strength, modules, elongation and hardness.
These values can be further improved by adjustments to the formulation. The product properties would depend on the actual formulation being cured and the curing conditions.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
Those skilled in the art will appreciate that the invention described herein is susceptible to variations and modifications other than those specifically described. It is to be understood that the invention includes all such ~rariations and modifications which fall within its spirit and scope. The invention also includes all of the steps, features, compositions and compounds referred to or indicated in this sp~;cification, individually or collectively, and any and all combinations of any two or more of said steps or features.
Preferred embodiments of the present invention will now be described in more detail with reference to the following examples which should not be construed as limiting on the invention in any way.
PrP,~garation of sulfur solution 1000g of oleic acid was introduced to a cold reactor and 250g of powered ventilated sulfur was added thereto with stirring. The reactor was closed with continual mixing of the solution. The solution was then heated to between 160°C and 180°C to completely dissolve the sulfur in the oleic acid. The s~~lution is then allowed to cool.
Throughout the heating process, ~:he solution was periodically checked to see whether the sulfur had dissolved. Generally, the solution was checked at about 150°C, 160°C and 170°C
by placing a drop of the liquid on a glass plate. If the drop was not clear, the sulfur was not completely dissolved. Heating was. continued until a clear and transparent drop was achieved on the glass plate.
Care should be taken when preparing the sulfur solution to evacuate or eliminate any sulfur dioxide gas produced. This may 1>e achieved through an exhaust fan or by using a caustic vapour trap.
1. Rubber Devulcanization Process Car tyre crumb rubber particles and chemical additives were weighed to the specified formulation. The ingredients were well mixed in a rotational mixer. The blend was then placed in layers in a device and heated. The resulting product was then milled on a two roll mill.
For truck tyre crumb rubber particles, the same procedure was followed.
2. Preparation of Rubber Samples The treated rubber was mixed with curatives at three levels, viz Car lyre samp).e:
{a) 50 % dewlcanized rubber and 50 % virgin uncured tyre tread (mainly natural rubber).
(b) 60% dewlcanized rwbber and 40% virgin uncured tyre tread.
{c) 30% dewlcanized »bber and 70% virgin uncured tyre tread.
Truck tyre sample:
(d) 50 % treated rubber and 50 % virgin uncured tyre tread {mainly natural rubber).
(e) 60 % treated rubber and 40 % virgin uncured tyre tread.
(f) 30 % treated rubber and 70 % virgin uncured tyre tread.
The above car and truck tyre samples were processed on a two roll mill and there were no processing difficulties encountered. The treated rubber blended with the virgin tyre stock without difficulties.
The samples were cured under normal curing conditions for truck tyres in a compression press.
3. Sample Evaluation 3.1 $~ecimen Preparation and Conditioning Test specimens were cut to ASTM D412 Die C from cured samples and conditioned at 23 ° C, 50 % humidity for 24 hours .
S
3.2 Testing Conditions Testing machine: LLOYD 20008 with computer interface;
Testing speed: 500 ;mm/min Temperature: 23 °C:
Humidity: 50%
Specimens tested: 3 for each sample 3.3 Test Results The average results are summarised in the following table.
Car T,~~re Sample LD. Tensile Modulus (Mpa)Elongation Hardness at (Devulcanized Strength at 300% Break (%) (Shore A) rubber/tyre (Mpa) Elongation tread stock) (a) (50/50) 4.29 2.57 463.6 56.8 (b) (60/40) 4.74 2.76 489.7 56.4 (c) (30/70) 7.23 2.61 702.4 58.0 Sample LD. Tensile Modulus Elongation Hardness at (DevulcanizedStrength (Mpa) at Break (%) (Shore A) rubber/tyre (Mpa) 300%
tread stock) Elongation (d) (50/50) 6.5 3.0 559.4 59 (e) (60/40) 7.2 3.3 586.1 58 (f) (30/70) 9.8 2.7 803.3 61 _g_ Conclusion The rubber devulcanization process is capable of producing a product that is compatible with rubber compounds. The performsmce of these compounds can be optimised with regard to the cure system, polymer type, filler level, sulfur level and level of addition of the devulcanized material.
The tests conducted show that :including . 30% of devulcanized material derived from passenger tyres into a tread formulation has resulted in a material with useful properties, i.e.
significant tensile strength, modules, elongation and hardness.
These values can be further improved by adjustments to the formulation. The product properties would depend on the actual formulation being cured and the curing conditions.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
Those skilled in the art will appreciate that the invention described herein is susceptible to variations and modifications other than those specifically described. It is to be understood that the invention includes all such ~rariations and modifications which fall within its spirit and scope. The invention also includes all of the steps, features, compositions and compounds referred to or indicated in this sp~;cification, individually or collectively, and any and all combinations of any two or more of said steps or features.
Claims (30)
1. A method for the treatment of vulcanized rubber comprising the steps of:
providing a solution of sulfur in a fatty acid or ester or a salt thereof;
blending the solution with particulate vulcanized rubber; and heating the blend for a time period and at a sufficient temperature and pressure to substantially devulcanize the rubber.
providing a solution of sulfur in a fatty acid or ester or a salt thereof;
blending the solution with particulate vulcanized rubber; and heating the blend for a time period and at a sufficient temperature and pressure to substantially devulcanize the rubber.
2. A method according to claim 1, wherein an oil-base softening agent is added to the blend prior to heating of the blend to soften the rubber during treatment.
3. A method according to claim 2, wherein the softening agent is an aromatic oil.
4. A method according to claim 1, wherein, during blending of the vulcanized rubber with the solution, the blend is cooled.
5. A method according to claim 4, wherein the blend is cooled by water cooling a mixing vessel in which the vulcanized rubber and the solution are being blended.
6. A method according to claim 1, wherein the blend is heated for a time period of from about 1 hour to about 8 hours.
7. A method according to claim 6, wherein the blend is heated for a time period of from about 4 to about 8 hours.
8. A method according to claim 1, wherein the blend is heated at a temperature of from about 180°-C to about 200°-C.
9. A method according to claim 1, wherein the treatment is carried out at a pressure of from about 18 to about 20 kg/cm2.
10. A method according to claim l, wherein the blend comprise about 100 parts particulate rubber, 4 to 6 parts softening agent and 2 to 4 parts treatment solution.
11. A method according to claim 1, wherein the particulate rubber is rubber crumb having a particle size of less than 6mm.
12. A method according to claim 1, wherein the particulate rubber is powdered rubber.
13. A method according to claim 1, wherein the solution of sulfur and fatty acid or ester or salt thereof comprises a solution of sulfur and fatty acid or ester or salt thereof in a ratio of 1:4.
14. A method according to claim 1, wherein the fatty acid or ester or salt thereof is an unsaturated fatty acid or ester or salt thereof.
15. A method according to claim 14, wherein the fatty acid is oleic acid.
16. A method according to claim 1, wherein the treatment solution is prepared by adding powdered ventilated sulfur to oleic acid which has been heated to approximately to 160°C while stirring the solution and increasing the temperature of the solution until the sulfur is completely dissolved in the oleic acid.
17. A method according to claim 16, wherein the temperature of the solution is increased to about 180°C to dissolve the sulfur in the oleic acid.
18. A method according to claim 1, wherein heating of the blend is achieved in an autoclave.
19. A method according to claim 18, wherein said autoclave is a rotating autoclave.
20. A method according to claim 1, wherein said method is earned out as a continuous process comprising a number of treatment stages.
21. A method according to claim 1, wherein following heating the blend is cooled or allowed to cool and wherein the cooled blend is then transferred to a milling station where it is milled one or more times, optionally with water cooling.
22. A method according to claim 21, wherein cooled blend is milled at least three times.
23. A method according to claim 21, wherein the milled rubber is cooled and then heated up to about 130°C, recooled and remilled.
24. A solution for treating vulcanized rubber, the solution comprising:
a fatty acid or ester or a salt thereof; and sulfur.
a fatty acid or ester or a salt thereof; and sulfur.
25. A solution according to claim 24, additionally comprising an oil-base softening agent.
26. A solution according to claim 25, wherein the softening agent is an aromatic oil.
27. A solution according to claim 25, comprising about 100 parts particulate rubber, 4 to 6 parts softening agent and 2 to 4 parts treatment solution.
28. A solution according to claim 24, comprising said sulfur and fatty acid or ester or salt thereof in a ratio of 1:4.
29. A solution according to claim 24, wherein the fatty acid or ester or salt thereof is an unsaturated fatty acid or ester or salt thereof.
30. A solution according to claim 29, wherein the fatty acid is oleic acid.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPP6275A AUPP627598A0 (en) | 1998-10-01 | 1998-10-01 | Method for treatment of vulcanized rubber |
| AUPP6275 | 1998-10-01 | ||
| PCT/AU1999/000845 WO2000020461A1 (en) | 1998-10-01 | 1999-10-01 | Method for treatment of vulcanized rubber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2346022A1 true CA2346022A1 (en) | 2000-04-13 |
Family
ID=3810493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2346022 Abandoned CA2346022A1 (en) | 1998-10-01 | 1999-10-01 | Method for treatment of vulcanized rubber |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP1127078A4 (en) |
| JP (1) | JP2002526606A (en) |
| KR (1) | KR20010088837A (en) |
| CN (1) | CN1326469A (en) |
| AP (1) | AP2001002130A0 (en) |
| AU (1) | AUPP627598A0 (en) |
| BR (1) | BR9914218A (en) |
| CA (1) | CA2346022A1 (en) |
| CZ (1) | CZ20011180A3 (en) |
| HK (1) | HK1038758A1 (en) |
| IL (1) | IL142352A0 (en) |
| MX (1) | MXPA01003341A (en) |
| NZ (1) | NZ511418A (en) |
| RU (1) | RU2001111822A (en) |
| TR (1) | TR200100924T2 (en) |
| WO (1) | WO2000020461A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015061895A1 (en) * | 2013-10-29 | 2015-05-07 | 6732667 Manitoba Inc. | Automatic devulcanizing and plasticizing device and method for using same |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6426136B1 (en) | 1998-02-10 | 2002-07-30 | R & D Technology, Inc. | Method of reducing material size |
| US6333373B1 (en) * | 1999-02-10 | 2001-12-25 | R&D Technology, Inc. | Ground elastomer and method |
| US6743836B2 (en) | 2000-01-26 | 2004-06-01 | R&D Technology, Inc. | Method for predispersing compounding ingredients |
| US6815510B2 (en) | 2001-11-19 | 2004-11-09 | Michael W. Rouse | Elastomer reclaiming composition and method |
| JP2011153272A (en) * | 2010-01-28 | 2011-08-11 | Bridgestone Corp | Method for decomposing and recovering vulcanized rubber |
| US10179479B2 (en) | 2015-05-19 | 2019-01-15 | Bridgestone Americas Tire Operations, Llc | Plant oil-containing rubber compositions, tread thereof and race tires containing the tread |
| JP7283797B2 (en) * | 2021-10-01 | 2023-05-30 | 公立大学法人公立鳥取環境大学 | Method for producing softened rubber |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2809944A (en) * | 1956-06-11 | 1957-10-15 | Us Rubber Reclaiming Co | Processes for the reclaiming of rubber and for the production of hard rubber products and the like, and the products thereof |
| JPS5558234A (en) * | 1978-10-25 | 1980-04-30 | Bridgestone Corp | Vulcanizable rubber composition |
| JPS6243441A (en) * | 1985-08-21 | 1987-02-25 | Riken Vitamin Co Ltd | Rubber compounded composition |
| US4895911A (en) * | 1988-10-06 | 1990-01-23 | The Goodyear Tire & Rubber Company | Tall oil fatty acid mixture in rubber |
| JPH0331335A (en) * | 1989-06-28 | 1991-02-12 | Nippon Zeon Co Ltd | Rubber composition |
-
1998
- 1998-10-01 AU AUPP6275A patent/AUPP627598A0/en not_active Abandoned
-
1999
- 1999-10-01 RU RU2001111822/04A patent/RU2001111822A/en not_active Application Discontinuation
- 1999-10-01 CN CN99813353A patent/CN1326469A/en active Pending
- 1999-10-01 CZ CZ20011180A patent/CZ20011180A3/en unknown
- 1999-10-01 EP EP19990952157 patent/EP1127078A4/en not_active Withdrawn
- 1999-10-01 IL IL14235299A patent/IL142352A0/en unknown
- 1999-10-01 JP JP2000574572A patent/JP2002526606A/en active Pending
- 1999-10-01 MX MXPA01003341A patent/MXPA01003341A/en unknown
- 1999-10-01 AP APAP/P/2001/002130A patent/AP2001002130A0/en unknown
- 1999-10-01 BR BR9914218A patent/BR9914218A/en not_active IP Right Cessation
- 1999-10-01 TR TR200100924T patent/TR200100924T2/en unknown
- 1999-10-01 NZ NZ511418A patent/NZ511418A/en not_active IP Right Cessation
- 1999-10-01 WO PCT/AU1999/000845 patent/WO2000020461A1/en not_active Application Discontinuation
- 1999-10-01 KR KR1020017004230A patent/KR20010088837A/en not_active Application Discontinuation
- 1999-10-01 CA CA 2346022 patent/CA2346022A1/en not_active Abandoned
-
2002
- 2002-01-10 HK HK02100181.7A patent/HK1038758A1/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015061895A1 (en) * | 2013-10-29 | 2015-05-07 | 6732667 Manitoba Inc. | Automatic devulcanizing and plasticizing device and method for using same |
Also Published As
| Publication number | Publication date |
|---|---|
| HK1038758A1 (en) | 2002-03-28 |
| RU2001111822A (en) | 2003-07-20 |
| EP1127078A1 (en) | 2001-08-29 |
| AUPP627598A0 (en) | 1998-10-22 |
| EP1127078A4 (en) | 2002-10-31 |
| KR20010088837A (en) | 2001-09-28 |
| WO2000020461A1 (en) | 2000-04-13 |
| TR200100924T2 (en) | 2001-08-21 |
| IL142352A0 (en) | 2002-03-10 |
| BR9914218A (en) | 2002-04-23 |
| AP2001002130A0 (en) | 2001-06-30 |
| MXPA01003341A (en) | 2003-05-15 |
| CN1326469A (en) | 2001-12-12 |
| JP2002526606A (en) | 2002-08-20 |
| NZ511418A (en) | 2002-07-26 |
| CZ20011180A3 (en) | 2001-10-17 |
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| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |