
Gas liberation 
                                During the irradiation of polyethylene a gas mixture is formed that consists of 98 % hydrogen, whilst the remaining gasses are the aliphatic compounds methane, ethane, propane and butane. It was shown that these saturated hydrocarbons result from the radiation degradation of the side chain branches of the polymer, as little main chain scission takes place. 
                                

Change in nature of unsaturation 
                                

Change in nature of unsaturation 
  It was observed that vinylidene and vinyl unsaturation that is present in the polyethylene, disappears even at very low irradiation doses. This is accompanied by an increase in the 
trans -vinylene unsaturation and the liberation of hydrogen gas. It is accepted that this trans -vinylene unsaturation is the result of a process of hydrogen abstraction from the hydrocarbon polymer chain.
  

Cross linking of polymer 
  

Cross linking of polymer 
The polymeric free radicals formed during the irradiation of polyethylene can combine to form the well known cross linking in the polymer. This effect is by far the best known because of its significant impact on the properties of the irradiated polymer. This cross linking can be either 
inter  or 
intra  molecular in nature � referred to as 
H- linking. The type of crosslinking having little effect on the change in polymer properties because of the entanglement of the polymeric molecules. 

Introduction of long chain branching 

Introduction of long chain branching 
An effect that received far less industrial attention than cross linking when irradiating polyethylene, is the enhancement of the long-chain branching (eight C-atoms or more) in the polymer � the so called Y-branching. This results in a broadening of the molecular weight distribution in the irradiated polymer and a lowering of the hydrodynamic volume of the polymer � both effects having significant implications on the properties and processing of such an irradiated polyethylene. It is thus possible to modify the molecular weight distribution, as well as change the ratio between long-chain branching and short-chain branching, by irradiating the polyethylene.

Change in rheological properties 

Change in rheological properties 
Cross linking in polyethylene during irradiation at ambient temperatures takes place predominantly in the amorphous phase of the polymer, with little cross linking in the crystalline regions of the polymer � the inhomogeneous cross-link distribution mentioned earlier. The melt-flow index of the irradiated polyethylene rapidly decreases with an increase in the irradiation dose, however, the corresponding spiral flow remains virtually independent of the irradiation dose � indicative of the long-chain branching and the associated broadening in the molecular weight distribution. These effects cause the difference in characteristics between radiation-induced and chemical crosslinking of polyethylene. 

Oxidation when irradiated in air 

Oxidation when irradiated in air 
The last radiation-induced effect in polyethylene that received little industrial attention, is the 
oxidation  of the polymer when irradiated in air. Apart from the crosslinking thereof, the radiation treatment of polyethylene in air results in a radiation-induced oxidation of the polymer rendering it with polar functional groups. This results in the modified polymer having adhesive properties to polar materials such as metals � a unique feature for PE.

Physical characteristics: 

Physical characteristics: 
In addition to the radiation-induced characteristics mentioned earlier, it should be noted that by cross linking the polymer the following properties can be improved: 

 Thermal:   

 Thermal:   
Dimensional stability 
Tensile deformation
Pressure deformation
Environmental stress cracking 
Melt strength
Memory effect

 Mechanical:

 Mechanical:
Cold flow 
Abrasion resistance
Modulus
Tensile and bending strength
Impact resistance
Hydrostatic stress strength
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