Information About

Polycarbonate


































Polycarbonate
Density 1220 Kg/m3
Young's Modulus (E)2-2.2 G Pa
Tensile Strengtht)60-65 M Pa
Elongation @ break80-150%
notch test20-35 K J / M 2
Glass Temperature 150° C
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Vicat B145
heat transfer coefficient (λ)0.21 W/ M . K
Linear Expansion Coefficient (α) 6.5 10-5 / K
Specific Heat (c)1.3 K J / Kg . K
Water absorption (ASTM)0.16
Price5-9 €/ Kg




Polycarbonates are a particular group of Thermoplastic s. They are easily worked, Molded , and Thermoformed ; as such, these Plastic s are very widely used in modern Manufacturing . They are called '''polycarbonates''' because they are Polymer s having functional groups linked together by Carbonate Group s (-O-CO-O-) in a long molecular chain.

The most common type of polycarbonate plastic is one made from Bisphenol A , in which groups from Bisphenol A are linked together by carbonate groups in a polymer chain. This polycarbonate is a very durable material, and can be laminated to make Bullet-proof "glass" , though “bullet-resistant” would be more accurate. The characteristics of polycarbonate are quite like those of Polymethyl Methacrylate ('' PMMA ''; '' Acrylic ''), but polycarbonate is stronger and more expensive. This Polymer is highly Transparent to Visible Light and has better light transmission characteristics than many kinds of Glass . CR-39 is a specific polycarbonate material with good optical and mechanical properties, frequently used for eyeglass lenses.

Polycarbonate has :

Polycarbonate is becoming more common in housewares as well as laboratories and in industry. It is often used to create protective features, for example in banks as well as vandal-proof windows and lighting lenses for many buildings. Other products made from polycarbonate include sunglass/eyeglass lenses, Compact Disc s, DVD s, and automotive headlamp lenses. It is the major component of one variety of Nalgene bottles. It is also used for animal enclosures and cages used in research.

LEXAN® is the registered trademark for polycarbonate plastic manufactured (from Bisphenol A) by General Electric . MERLON® is the registered trademark used by the Mobay Chemical Company . MAKROLON® is the registered trademark for polycarbonate from Bayer , which is also referred to as "macrolon". PANLITE® is the registered trademark for polycarbonate plastic manufactured from Teijin Chemical Limited, which is also the major producer for optical grade polycarbonate.


POTENTIAL HAZARDS IN FOOD CONTACT APPLICATIONS


Polycarbonate may be appealing to fabricators and purchasers of food storage containers due to its clarity and toughness. Polycarbonate has been described as lightweight and highly break resistant particularly when compared to silica Glass . Polycarbonate may be seen in the form of single use and refillable plastic water bottles.

More than 100 studies have explored the bioactivity of Bisphenol A leachates from polycarbonates. Howdeshell et. al. found that Bisphenol A appeared to be released from polycarbonate animal cages into water at room temperature and that it may have been responsible for enlargement of the reproductive organs of female mice.
http://ehp.niehs.nih.gov/members/2003/5993/5993.html

An analysis of the literature on Bisphenol A leachate low-dose effects by vom Saal and Hughes published in August 2005 seems to have found a suggestive correlation between the source of funding and the conclusion drawn. Industry funded studies appear to tend to find no significant effects while government funded studies tend to find significant effects.
http://ehp.niehs.nih.gov/docs/2005/7713/abstract.html


SYNTHESIS

Polycarbonate can be synthesized from Bisphenol A and Phosgene (carbonyl dichloride, COCl2). The first step in the synthesis of polycarbonate from bisphenol A is treatment of bisphenol A with Sodium Hydroxide . This deprotonates the Hydroxyl Group s of the bisphenol A Molecule .



The deprotonated oxygen reacts with phosgene through carbonyl addition to create a Tetrahedral intermediate (not shown here), after which the negatively charged oxygen kicks off a Chloride Ion (Cl-) to form a Chloroformate .



The chloroformate is then attacked by another deprotonated bisphenol A, eliminating the remaining chloride ion and forming a dimer of bisphenol A with a carbonate linkage in between.



Repetition of this process yields polycarbonate, a polymer with alternating carbonate groups and groups from bisphenol A. Density starts at about 1.20 g/cm3.


INTERACTION WITH OTHER CHEMICALS


Using Sodium Hydroxide and other alkali cleaners on polycarbonate is not recommended as they cause the release of Bisphenol-A , a known Endocrine disrupter.


EXTERNAL LINK