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Specialty Polyamides
Market Focus Presentation
Market Focus
Fragrance Carriers
2
Specific applications
Air fresheners
Aroma candles
Fire-less candles
Toilet cleaners
Tablets for dishwasher
Scented/flavored dental floss
Insect repellants
Wearable & non-wearable
Cow tags
Pet collars
3
Challenges for the industry
Uniform distribution of fragrance
Selected rate of distribution
Too quick
Short lifespan of fragrance
Undesirable intense aroma
Too slow
Insufficient aroma for large area
Ineffective for intended use
4
5
High performance options
PolyEther Block Amides
Thermoplastic elastomer
Pebax® resin advantages
Selective absorption
Polyether phase accepts many volatile molecules
Good absorption up to 50%
Controlled release
Manipulate diffusion with wall thickness and temperature
Very good retention of fragrance properties
Strong mechanical structure
Preserved by polyamide block
Low melting point
Molding and extrusion without degrading the fragrance substances
Easy processing
Save time and reduce costs with more efficient processing
6
Comparison data
7
Reference
Pebax® 2533
SA01
Cellulose EVA 2825
% Absorption 50 70 20
% Lavender
after 60 days 11 3 2
Controlled diffusion
with Pebax® resin
0 10 20 30 40 50 60 70
Diffusion of Lavender
Pebax® 2533 SA01
Cellulose
EVA 2825
%Lavender
Days
Comparison data
8
0
10
20
30
40
50
60
70
80
0 10 20 30 40 50 60
Areas
Days
Evolution of lavender fragrance
– Chromatography test
Pebax® 2533 SA01
Cellulose
Fragrance properties
sustained within
Pebax® resins
Grade selection
Pebax® 2533 SA01 is recommended
for fragrance carrier applications
9
More information & contact details
www.arkema.com
www.pebax.com
info.polyamides@arkema.com
10
11
Disclaimer
The statements, technical information and recommendations contained herein are believed to be accurate as of the date hereof. Since
the conditions and methods of use of the product and of the information referred to herein are beyond our control, ARKEMA expressly
disclaims any and all liability as to any results obtained or arising from any use of the product or reliance on such information; NO
WARRANTY OF FITNESS FOR ANY PARTICULAR PURPOSE, WARRANTY OF MERCHANTABILITY OR ANY OTHER WARRANTY, EXPRESSED OR
IMPLIED, IS MADE CONCERNING THE GOODS DESCRIBED OR THE INFORMATION PROVIDED HEREIN. The information provided herein relates
only to the specific product designated and may not be applicable when such product is used in combination with other materials or in
any process. The user should thoroughly test any application before commercialization. Nothing contained herein constitutes a license to
practice under any patent and it should not be construed as an inducement to infringe any patent and the user is advised to take
appropriate steps to be sure that any proposed use of the product will not result in patent infringement. See SDS for Health & Safety
Considerations.
Arkema has implemented a Medical Policy regarding the use of Arkema products in Medical Devices applications that are in contact with
the body or circulating bodily fluids (http://www.arkema.com/en/social-responsibility/responsibleproduct-management/medical-device-
policy/index.html) Arkema has designated Medical grades to be used for such Medical Device applications. Products that have not been
designated as Medical grades are not authorized by Arkema for use in Medical Device applications that are in contact with the body or
circulating bodily fluids. In addition, Arkema strictly prohibits the use of any Arkema products in Medical Device applications that are
implanted in the body or in contact with bodily fluids or tissues for greater than 30 days. The Arkema trademarks and the Arkema name
shall not be used in conjunction with customers' medical devices, including without limitation, permanent or temporary implantable
devices, and customers shall not represent to anyone else, that Arkema allows, endorses or permits the use of Arkema products in such
medical devices.
It is the sole responsibility of the manufacturer of the medical device to determine the suitability (including biocompatibility) of all raw
materials, products and components, including any medical grade Arkema products, in order to ensure that the final end-use product is
safe for its end use; performs or functions as intended; and complies with all applicable legal and regulatory requirements (FDA or other
national drug agencies) It is the sole responsibility of the manufacturer of the medical device to conduct all necessary tests and inspections
and to evaluate the medical device under actual end-use requirements and to adequately advise and warn purchasers, users, and/or
learned intermediaries (such as physicians) of pertinent risks and fulfill any postmarket surveillance obligations. Any decision regarding the
appropriateness of a particular Arkema material in a particular medical device should be based on the judgment of the manufacturer,
seller, the competent authority, and the treating physician.
Rilsan®, Rilsamid®, Pebax ®, Hiprolon ®, Platamid ®, Orgalloy ® and Orgasol ® are registered trademarks of Arkema

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Arkema Specialty Polyamides for Fragrance Carriers

  • 3. Specific applications Air fresheners Aroma candles Fire-less candles Toilet cleaners Tablets for dishwasher Scented/flavored dental floss Insect repellants Wearable & non-wearable Cow tags Pet collars 3
  • 4. Challenges for the industry Uniform distribution of fragrance Selected rate of distribution Too quick Short lifespan of fragrance Undesirable intense aroma Too slow Insufficient aroma for large area Ineffective for intended use 4
  • 5. 5 High performance options PolyEther Block Amides Thermoplastic elastomer
  • 6. Pebax® resin advantages Selective absorption Polyether phase accepts many volatile molecules Good absorption up to 50% Controlled release Manipulate diffusion with wall thickness and temperature Very good retention of fragrance properties Strong mechanical structure Preserved by polyamide block Low melting point Molding and extrusion without degrading the fragrance substances Easy processing Save time and reduce costs with more efficient processing 6
  • 7. Comparison data 7 Reference Pebax® 2533 SA01 Cellulose EVA 2825 % Absorption 50 70 20 % Lavender after 60 days 11 3 2 Controlled diffusion with Pebax® resin 0 10 20 30 40 50 60 70 Diffusion of Lavender Pebax® 2533 SA01 Cellulose EVA 2825 %Lavender Days
  • 8. Comparison data 8 0 10 20 30 40 50 60 70 80 0 10 20 30 40 50 60 Areas Days Evolution of lavender fragrance – Chromatography test Pebax® 2533 SA01 Cellulose Fragrance properties sustained within Pebax® resins
  • 9. Grade selection Pebax® 2533 SA01 is recommended for fragrance carrier applications 9
  • 10. More information & contact details www.arkema.com www.pebax.com info.polyamides@arkema.com 10
  • 11. 11 Disclaimer The statements, technical information and recommendations contained herein are believed to be accurate as of the date hereof. Since the conditions and methods of use of the product and of the information referred to herein are beyond our control, ARKEMA expressly disclaims any and all liability as to any results obtained or arising from any use of the product or reliance on such information; NO WARRANTY OF FITNESS FOR ANY PARTICULAR PURPOSE, WARRANTY OF MERCHANTABILITY OR ANY OTHER WARRANTY, EXPRESSED OR IMPLIED, IS MADE CONCERNING THE GOODS DESCRIBED OR THE INFORMATION PROVIDED HEREIN. The information provided herein relates only to the specific product designated and may not be applicable when such product is used in combination with other materials or in any process. The user should thoroughly test any application before commercialization. Nothing contained herein constitutes a license to practice under any patent and it should not be construed as an inducement to infringe any patent and the user is advised to take appropriate steps to be sure that any proposed use of the product will not result in patent infringement. See SDS for Health & Safety Considerations. Arkema has implemented a Medical Policy regarding the use of Arkema products in Medical Devices applications that are in contact with the body or circulating bodily fluids (http://www.arkema.com/en/social-responsibility/responsibleproduct-management/medical-device- policy/index.html) Arkema has designated Medical grades to be used for such Medical Device applications. Products that have not been designated as Medical grades are not authorized by Arkema for use in Medical Device applications that are in contact with the body or circulating bodily fluids. In addition, Arkema strictly prohibits the use of any Arkema products in Medical Device applications that are implanted in the body or in contact with bodily fluids or tissues for greater than 30 days. The Arkema trademarks and the Arkema name shall not be used in conjunction with customers' medical devices, including without limitation, permanent or temporary implantable devices, and customers shall not represent to anyone else, that Arkema allows, endorses or permits the use of Arkema products in such medical devices. It is the sole responsibility of the manufacturer of the medical device to determine the suitability (including biocompatibility) of all raw materials, products and components, including any medical grade Arkema products, in order to ensure that the final end-use product is safe for its end use; performs or functions as intended; and complies with all applicable legal and regulatory requirements (FDA or other national drug agencies) It is the sole responsibility of the manufacturer of the medical device to conduct all necessary tests and inspections and to evaluate the medical device under actual end-use requirements and to adequately advise and warn purchasers, users, and/or learned intermediaries (such as physicians) of pertinent risks and fulfill any postmarket surveillance obligations. Any decision regarding the appropriateness of a particular Arkema material in a particular medical device should be based on the judgment of the manufacturer, seller, the competent authority, and the treating physician. Rilsan®, Rilsamid®, Pebax ®, Hiprolon ®, Platamid ®, Orgalloy ® and Orgasol ® are registered trademarks of Arkema