WO2008087675A1 - Styrenic block copolymer plasticised with vegetable oils and process for preparing same - Google Patents

Styrenic block copolymer plasticised with vegetable oils and process for preparing same Download PDF

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Publication number
WO2008087675A1
WO2008087675A1 PCT/IT2007/000184 IT2007000184W WO2008087675A1 WO 2008087675 A1 WO2008087675 A1 WO 2008087675A1 IT 2007000184 W IT2007000184 W IT 2007000184W WO 2008087675 A1 WO2008087675 A1 WO 2008087675A1
Authority
WO
WIPO (PCT)
Prior art keywords
styrene
styrenic block
oils
block copolymers
vegetal
Prior art date
Application number
PCT/IT2007/000184
Other languages
French (fr)
Inventor
Bruno Cardinali
Original Assignee
Tecnocompounds Valtenna S.R.L.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tecnocompounds Valtenna S.R.L. filed Critical Tecnocompounds Valtenna S.R.L.
Publication of WO2008087675A1 publication Critical patent/WO2008087675A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • C08K5/103Esters; Ether-esters of monocarboxylic acids with polyalcohols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • C08L53/025Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes modified

Definitions

  • the present invention relates to a plastification process of thermoplastic elastomers derived from styrenic block copolymers, in which vegetal oils are used as. plastifying substances.
  • the present invention also relates to the thermoplastic elastomers obtained with the said process.
  • SBS Styrene-butadiene-styrene
  • SIS styrene-isoprene-styrene
  • SIBS styrene-isoprene-butadiene-styrene
  • SEBS Styrene-butadiene-styrene
  • SEBS hydrogenated derivatives
  • thermoplastic elastomeric materials They have a considerably advantageous application compared to vulcanised elastomers and therefore they are more and more used, reducing the market share of cross-linked rubbers.
  • Another problem refers to the manufacturing of products that come in contact with the human body: pharmaceutical or oenological vaselines must be used with mineral plastifying agents, with high costs and consequent environmental problems.
  • organic plastifying agents such as oils that are extracted from a large variety of vegetal organisms, soya beans, corn, flax, etc.
  • mineral plastifying agents that is to say human contacts and biodegradability.
  • Many products, such as toys, children shoes, footstraps, slippers that come in direct contact with the skin will find the ideal solution for the human health.
  • the purpose of the present invention is to overcome the aforementioned problems and inconveniences. This purpose has been achieved with the process claimed in the first claim.
  • the said process consists in a traditional production process of thermoplastic elastomers derived from styrenic block copolymers, which uses for the first time vegetal oils as plastifying substances.
  • Vegetal seed oils are essentially triglycerides of saturated and unsaturated fat acids, therefore in a molecular chain of about 50 carbon atoms there are only
  • the relatively low polarity makes it possible to use the oil as plastifying agent of the paraffinic or paraffinic-olephinic chains between the styrenic blocks of styrene butadiene block or styrene-isoprene block copolymers (or similar products) without migration problems both in production and during product life.
  • Vegetal oil (Sunflower, Peanut, Palm mix) 80 parts by weight 35/35/30
  • Vegetal oils are preferably derived from: peanut, sunflower, flax, corn, soy, colza, sesame, palm, coconut, cashew.
  • the said vegetal oils are derived from vegetal organisms, such as leaves, roots, stems, bark, flowers.
  • the said vegetal oils are derived from a mix of two or more vegetal substances.
  • the said styrenic block copolymers can be either hydrogenated or non-hydrogenated.
  • non-hydrogenated copolymers the preferred ones belong to the following groups: SBS (Styrene-Butadiene-Styrene), SIS (Styrene, Isoprene,
  • hydrogenated copolymers the preferred ones belong to the following groups: SEBS (Styrene, EthyleneButylene-Styrene), SEPS (Styrene-
  • thermoplastic elastomers either organic or inorganic substances are added to the said thermoplastic elastomers.
  • Polyethylene polymers and their copolymers preferably EVA, EBA, EMA,
  • Polyethylene and derivatives preferably crystal and/or high impact, polybutadiene, syndiotactic 1 ,2, polyalphametylstyrene are preferred among organic substances.
  • inorganic substances talcum, kaolin, calcium carbonate.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Fats And Perfumes (AREA)

Abstract

The present invention relates to a plastification process of thermoplastic elastomers derived from styrenic block copolymers, in which vegetal oils are used as plastifying substances.

Description

STYRENIC BLOCK COPOLYMER PLASTICISED WITH VEGETABLE OILS AND PROCESS FOR PREPARING SAME
The present invention relates to a plastification process of thermoplastic elastomers derived from styrenic block copolymers, in which vegetal oils are used as. plastifying substances. The present invention also relates to the thermoplastic elastomers obtained with the said process. SBS (Styrene-butadiene-styrene), SIS (styrene-isoprene-styrene), SIBS (styrene-isoprene-butadiene-styrene) block copolymers and hydrogenated derivatives (SEBS, SEPS etc.), are usually plastified with mineral oils of paraffinic type with a low content of aromatic products. When suitably compounded with additives, either organic or inorganic, they are used in many industrial sectors, from footwear to car components, from toys to gaskets.
Being thermoplastic elastomeric materials, they have a considerably advantageous application compared to vulcanised elastomers and therefore they are more and more used, reducing the market share of cross-linked rubbers.
One of the problems of vulcanised elastomeric products is poor biodegradability, since the presence of mineral oils in the products enormously reduces their environmental degradability capacity. Another problem refers to the manufacturing of products that come in contact with the human body: pharmaceutical or oenological vaselines must be used with mineral plastifying agents, with high costs and consequent environmental problems.
The use of organic plastifying agents, such as oils that are extracted from a large variety of vegetal organisms, soya beans, corn, flax, etc., contributes to solve the problems caused by mineral plastifying agents, that is to say human contacts and biodegradability. Many products, such as toys, children shoes, footstraps, slippers that come in direct contact with the skin will find the ideal solution for the human health.
The purpose of the present invention is to overcome the aforementioned problems and inconveniences. This purpose has been achieved with the process claimed in the first claim. The said process consists in a traditional production process of thermoplastic elastomers derived from styrenic block copolymers, which uses for the first time vegetal oils as plastifying substances.
Description of the invention.
Vegetal seed oils are essentially triglycerides of saturated and unsaturated fat acids, therefore in a molecular chain of about 50 carbon atoms there are only
3 ester groups that give a limited general chemical polarity of the product.
The relatively low polarity makes it possible to use the oil as plastifying agent of the paraffinic or paraffinic-olephinic chains between the styrenic blocks of styrene butadiene block or styrene-isoprene block copolymers (or similar products) without migration problems both in production and during product life.
Most of all, no dissolution phenomena of styrenic domains with reduction of general elastomeric characteristics are found; in fact, tension, elongation and elastic return tests have not shown considerable differences with respect to compounds produced with mineral oils.
Thermal resistance tests on samples at 55°C and -25° C have not shown any bleeding of oil products towards the external surface. The production process of compounds based on styrenic block copolymers plastified with vegetal oils perfectly follows the dynamics and logics of the corresponding compounds produced with mineral oils.
Initial absorption process of plastifying agent, addition of fillers of mineral origin (where necessary), addition of various polymer and non-polymer additives, addition of organic pigments and then extrusion with machines that are traditionally used for this type of elastomeric and non-elastomeric materials. EXAMPLE 1
Compound with high content of plastifying agent
Kg
SBS (Europrene SOL T 161 or equivalent ) 100 Colza and soya bean oil 50/50 80
Mix in agitator, slow or fast, for at least 5 minutes, than extrude the mix in a twin screw extruder configured for production of SBS compounds.
Mould the compound in a continuous screw or piston press, producing a specimen with suitable dimensions for physical-mechanical analyses.
The following results were obtained:
Results Method of Result Unit of measurement measurement
Hardness DIN 53505 30 SHORE A
Melt Flow Index DIN 53735 25 g/10' at 190° 5Kg
Tensile strength at DIN 53504 4,5 MPa break
Elongation at break DIN 53504 800 %
Bondability Internal method 6 N/mm
Bleeding Internal method none
Light tightness Internal method Usual as plastified SBS
Mineral OIL
Environmental External exposure Bacterial aggressions and mo stability after a few months
EXAMPLE 2
Kg
SBS (Dynasol 411 or equivalent) 70 SBS (Dynasol 501 or equivalent) 20
Crystal polystyrene 40
Syndiotactic 1 ,2 polybutadiene (RB 840) 40
Vegetal oil (Sunflower, Peanut, Palm mix) 80 parts by weight 35/35/30
Mix in agitator, slow or fast, for at least 5 minutes, than extrude the mix in a twin screw extruder configured for production of SBS compounds. Mould the compound in a continuous screw or piston press, producing a specimen with suitable dimensions for physical-mechanical analyses. The following results were obtained:
Results Method of Result Unit of measurement measurement
Hardness DIN 53505 65 SHORE A
Melt Flow Index DIN 53735 56 g/10' at 190° 5Kg
Tensile strength at DIN 53504 5,0 MPa break
Elongation at break DIN 53504 520 %
Abrasion DIN 53516 190 mm3
Bondability Internal method 8 N/mm
Bleeding Internal method none
Light tightness Internal method Usual as plastified SBS
Mineral OIL
Environmental External exposure Bacterial aggressions and mo stability after a few months
The following results are obtained when comparing the results of these compounds with the corresponding products obtained by replacing vegetal oil with traditional plastifying agent derived from mineral oil: tests
Compound degradation
SEED OIL bacterial aggression
MINERAL OIL non aggression
With reference to mechanical tests, compounds plastified with seed oil have shown the same results of compounds plastified with mineral oil.
Vegetal oils are preferably derived from: peanut, sunflower, flax, corn, soy, colza, sesame, palm, coconut, cashew. Alternatively, the said vegetal oils are derived from vegetal organisms, such as leaves, roots, stems, bark, flowers.
In another alternative solution, the said vegetal oils are derived from a mix of two or more vegetal substances.
It must be noted that the said styrenic block copolymers can be either hydrogenated or non-hydrogenated.
Among non-hydrogenated copolymers, the preferred ones belong to the following groups: SBS (Styrene-Butadiene-Styrene), SIS (Styrene, Isoprene,
Styrene).
Among hydrogenated copolymers, the preferred ones belong to the following groups: SEBS (Styrene, EthyleneButylene-Styrene), SEPS (Styrene-
EthylenePropylene-Styrene), SEEPS (Styrene EthyleneEthylenePropylene-
Styrene).
In a preferred embodiment of the process of the invention, either organic or inorganic substances are added to the said thermoplastic elastomers. Polyethylene polymers and their copolymers, preferably EVA, EBA, EMA,
Polyethylene and derivatives, preferably crystal and/or high impact, polybutadiene, syndiotactic 1 ,2, polyalphametylstyrene are preferred among organic substances.
The following substances are preferred among inorganic substances: talcum, kaolin, calcium carbonate.

Claims

Claims
1. Production process of thermoplastic elastomers derived from styrenic block copolymers, consisting in a first mixing stage and a second extrusion stage, characterised in that vegetal oils are used as plastifying substances;
2. process as claimed in claim 1 , characterised in that the said oils are preferably derived from seeds;
3. process as claimed in claim 2, characterised in that the said oils are preferably derived from peanut, sunflower, flax, corn, soya bean, colza, sesame, palm, coconut, cashew;
4. process as claimed in claim 1 , characterised in that the said oils are derived from vegetal organisms, such as leaves, roots, stems, bark, flowers;
5. process as claimed in one or more of above claims, characterised in that the said oils are derived either from a single vegetal substance or from a mix of two or more vegetal substances;
6. process as claimed in one or more of the preceding claims, characterised in that the said styrenic block copolymers are not hydrogenated;
7. process as claimed in above claim, characterised in that the said styrenic block copolymers belong to the following groups: - SBS (Styrene-Butadiene-Styrene)
- SIS (Styrene-Isoprene-Styrene)
8. process as claimed in one or more of claims 1 to 5, characterised in that the said styrenic block copolymers are hydrogenated;
9. process as claimed in above claim, characterised in that the said styrenic block copolymers belong to the following groups:
- SEBS (Styrene-EthyleneButylene-Styrene)
- SEPS (Styrene-EthylenePropylene-Styrene)
- SEEPS (Styrene-EthyleneEthylenePropylene-Styrene)
10. process as claimed in claim 1 , characterised in that mixing is performed in agitator for at least five minutes and extrusion is performed in a twin screw extruder configured for the production of SBS compounds;
11. thermoplastic elastomer derived from styrenic block copolymers obtained with a plastification process as the one described in claims 1 to 10;
12. thermoplastic elastomer as claimed in above claim, characterised in that it is mixed with traditional organic and inorganic additives
13. thermoplastic elastomer as claimed in above claim, characterised in that the said organic additives are Polyethylene polymers and copolymers, preferable EVA, EBA, EMA, Polystyrene and derivatives, preferably crystal and/or high impact, polybutadiene, syndiotactic 1 ,2, polyalphametylstyrene;
14. elastomer as claimed in claim 12, characterised in that the said inorganic additives are preferably talcum, kaolin, calcium carbonate;
15. thermoplastic elastomer as claimed in claim 11 , characterised in that it is obtained by mixing Kg
SBS (Eϋroprene SOL T 161 or equivalent 100
Colza and soya bean oil 50/50 80
16. thermoplastic elastomer as claimed in claim 11 , characterised in that it is obtained by mixing
Kg
SBS (Dynasol 411 or equivalent) 70
SBS (Dynasol 501 or equivalent) 20
Crystal polystyrene 40 Syndiotactic 1 ,2 polybutadiene (RB 840) 40
Vegetal oil (Sunflower, Peanut, Palm mix) 80 parts by weight 35/35/30
PCT/IT2007/000184 2007-01-19 2007-03-13 Styrenic block copolymer plasticised with vegetable oils and process for preparing same WO2008087675A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITMC2007A000010 2007-01-19
IT000010A ITMC20070010A1 (en) 2007-01-19 2007-01-19 PRODUCTION OF THERMOPLASTIC ELATOMERS WITH EXCELLENT ENVIRONMENTAL COMPATIBILITY CHARACTERISTICS OBTAINED THROUGH PLASTIFICATION WITH VEGETABLE OIL.

Publications (1)

Publication Number Publication Date
WO2008087675A1 true WO2008087675A1 (en) 2008-07-24

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2325255A1 (en) 2009-11-12 2011-05-25 Tecnofilm S.p.A. Biodegradable product obtained from compositions based on thermoplastic polymers
EP2395047A1 (en) 2010-04-16 2011-12-14 Tecnofilm S.p.A. Biodegradable polymers
CN102634109A (en) * 2012-05-08 2012-08-15 浦江县金太郎玩具有限公司 Expanding material for manufacturing expansion toy and manufacturing method of expanding material for manufacturing expansion toy
CN102649862A (en) * 2011-02-24 2012-08-29 泰克诺费尔姆股份公司 Biodegradable product obtained from thermoplastic polymer composite
EP2602282A1 (en) * 2011-12-05 2013-06-12 Nordenia Deutschland Gronau GmbH Elastic film for the nappy area
US20140100310A1 (en) * 2012-10-08 2014-04-10 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
WO2014058823A1 (en) 2012-10-08 2014-04-17 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
EP2759572A1 (en) 2013-01-23 2014-07-30 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
CN113583357A (en) * 2021-09-10 2021-11-02 山东小麦歌环保科技有限公司 Sanitary, safe and environment-friendly food packaging box and production method thereof
US20220016322A1 (en) * 2018-12-10 2022-01-20 Ineo-Tech Sdn Bhd Multilayer synthetic rubber compositions

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003080555A (en) * 2001-09-12 2003-03-19 Nok Corp Method for manufacturing cover integrated type gasket for hard disk driving
US20060121170A1 (en) * 2004-12-06 2006-06-08 Howard David L Rubbery gels made from vegetable oils

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003080555A (en) * 2001-09-12 2003-03-19 Nok Corp Method for manufacturing cover integrated type gasket for hard disk driving
US20060121170A1 (en) * 2004-12-06 2006-06-08 Howard David L Rubbery gels made from vegetable oils

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2325255A1 (en) 2009-11-12 2011-05-25 Tecnofilm S.p.A. Biodegradable product obtained from compositions based on thermoplastic polymers
US8293814B2 (en) 2009-11-12 2012-10-23 Tecnofilm S.P.A. Biodegradable product obtained from compounds of thermoplastic polymers
US8349914B2 (en) 2010-04-16 2013-01-08 Technofilm S.p.A. Biodegradable polymers and compounds
EP2395047A1 (en) 2010-04-16 2011-12-14 Tecnofilm S.p.A. Biodegradable polymers
CN102649862A (en) * 2011-02-24 2012-08-29 泰克诺费尔姆股份公司 Biodegradable product obtained from thermoplastic polymer composite
EP2602282A1 (en) * 2011-12-05 2013-06-12 Nordenia Deutschland Gronau GmbH Elastic film for the nappy area
CN102634109A (en) * 2012-05-08 2012-08-15 浦江县金太郎玩具有限公司 Expanding material for manufacturing expansion toy and manufacturing method of expanding material for manufacturing expansion toy
US20140100310A1 (en) * 2012-10-08 2014-04-10 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
WO2014058823A1 (en) 2012-10-08 2014-04-17 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
WO2014058822A1 (en) 2012-10-08 2014-04-17 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
US10125255B2 (en) 2012-10-08 2018-11-13 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
EP2759572A1 (en) 2013-01-23 2014-07-30 Teknor Apex Company Thermoplastic elastomer compositions having biorenewable content
US20220016322A1 (en) * 2018-12-10 2022-01-20 Ineo-Tech Sdn Bhd Multilayer synthetic rubber compositions
US11975124B2 (en) * 2018-12-10 2024-05-07 Ineo Tech Sdn Bhd Multilayer synthetic rubber compositions
CN113583357A (en) * 2021-09-10 2021-11-02 山东小麦歌环保科技有限公司 Sanitary, safe and environment-friendly food packaging box and production method thereof

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Publication number Publication date
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