Technical Data Sheet - ISO
Technical Data Sheet - ISO
Product Description
Lupolen 5261 Z is a high density polyethylene with high impact resistance, high rigidity, high
chemical resistance and good ESCR. It is delivered in powder form and contains antioxidants.
Typical customer applications include open top drums and jerry cans for the packaging of
dangerous goods. Lupolen 5261 Z is not intended for use in medical and pharmaceutical
applications.
Product Characteristics
Additional Properties
ESCR (FNCT 3.5 MPa / 80°C, 2% Arkopal N100)(ISO 16770): 12 h
Electric Strength (IEC 93, K20/P50): >150 kV/mm
Staudinger Index Jg (ISO 1628): 475 ml/g
Processing Temperature Range: 190 - 220 °C
Notes
Typical properties; not to be construed as specifications.
Further Information
Lupolen 5261 Z
Workers should be protected from the possibility of skin or eye contact with molten polymer.
Safety glasses are suggested as a minimal precaution to prevent mechanical or thermal injury to
the eyes.
Molten polymer may be degraded if it is exposed to air during any of the processing and off-line
operations. The products of degradation have an unpleasant odour. In higher concentrations they
may cause irritation of the mucus membranes. Fabrication areas should be ventilated to carry
away fumes or vapours. Legislation on the control of emissions and pollution prevention must be
observed. If the principles of sound manufacturing practice are adhered to and the place of work
is well ventilated, no health hazards are involved in processing the resin.
The resin will burn when supplied with excess heat and oxygen. It should be handled and stored
away from contact with direct flames and/or ignition sources. In burning the resin contributes
high heat and may generate a dense black smoke. Starting fires can be extinguished by water,
developped fires should be extinguished by heavy foams forming an aqueous or polymeric film.
The resins may be used for the production of dangerous goods packagings. It may happen that
these used and thus potentially contaminated packagings will be recycled and converted to
finished parts again. In order to avoid any resulting health, safety and environmental issues it is
the responsibility of the converter to take all the necessary precautions in that case.
For further information about safety in handling and processing please refer to the Material Safety
Data Sheet.
Storage:
The resin is packed in 25 kg bags or in bulk containers protecting it from contamination. If it is
stored under adverse conditions, i. e. if there are large fluctuations in ambient temperature and
the atmospheric humidity is high, moisture may condense inside the packaging. Under these
circumstances, it is recommended to dry the resin before use. Unfavourable storage conditions
may also intensify the resin´s slight characteristic odour.
The information submitted is based on our current knowledge and experience. In view of the
many factors that may affect processing and application, these data do not relieve processors of
the responsibility of carrying out their own tests and experiments; neither do they imply any
legally binding assurance of certain properties or of suitability for a specific purpose. The data do
not relieve the customer from his obligation to control the resin upon arrival and to complain
about faults. It is the responsibility of those to whom we supply our products to ensure that any
proprietary rights and existing laws and legislation are observed.
© LyondellBasell Industries Holdings, B.V. 2015
For the contact details of the LyondellBasell company selling this product in your country, please visit
http://www.lyb.com/.
Before using a product sold by a company of the LyondellBasell family of companies, users should make
their own independent determination that the product is suitable for the intended use and can be used
safely and legally. SELLER MAKES NO WARRANTY; EXPRESS OR IMPLIED (INCLUDING ANY WARRANTY
OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE OR ANY WARRANTY) OTHER THAN AS
SEPARATELY AGREED TO BY THE PARTIES IN A CONTRACT.
(i) any U.S. FDA Class I, Health Canada Class I, and/or European Union Class I Medical Devices, without
prior notification to Seller for each specific product and application; or
(ii) the manufacture of any of the following, without prior written approval by Seller for each specific
product and application: (1) U.S. FDA Class II, Health Canada Class II or Class III, and/or European
Union Class II Medical Devices; (2) film, overwrap and/or product packaging that is considered a part or
component of one of the aforementioned Medical Devices; (3) packaging in direct contact with a
pharmaceutical active ingredient and/or dosage form that is intended for inhalation, injection,
intravenous, nasal, ophthalmic (eye), digestive, or topical (skin) administration; (4) tobacco related
products and applications; (5) electronic cigarettes and similar devices; and (6) pressure pipe or fittings
that are considered a part or component of a nuclear reactor.
(iii) Additionally, the product(s) may not be used in: (1) U.S. FDA Class III, Health Canada Class IV,
and/or European Class III Medical Devices; (2) applications involving permanent implantation into the
body; (3) life-sustaining medical applications; and (4) lead, asbestos or MTBE related applications.
All references to U.S. FDA, Health Canada, and European Union regulations include another country's
equivalent regulatory classification.
Users should review the applicable Safety Data Sheet before handling the product.
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