Download presentation
Published byPrudence Shields Modified over 9 years ago
1
Vulcanization of Polymers & Biodegradable plastics
2
Structure of natural rubber
*Elastomer *Derived from latex *Polymer of isoprene *Molecular weight= *Some include other materials
3
Chemical Properties of natural rubber
*Polyene *C=C function e.g. addtion reactions *Ozonolysis of rubber *Pyrolysis of rubber
4
Vulcanization *Charles Goodyear (1800-1860)
*Chemical process -convert rubber,polymers into durable material *Irreversible *Cross-linkage -between polymer chains with sulphur *Benefit the industrial world
5
Process of Vulcanization
Cure sites -attractive to sulphur atoms Break down of 8-membered ring of sulphur Attachment of sulphur atoms to rubber molecule -one or more suphur atoms can be attached Reach the cure site of another rubber molecule
6
Methods of vulcanization
vulcanization of tires - high pressure and temperature - compression molding Hot air vulcanization Microwave heated vulcanization
7
Physical Properties VS Structure
-non-sticky, not easy to deform when warm, not brittle when cold , elastic *Relationship with structure - crosslinkage -polymer chains cannot move independently
8
Uses of vulcanized rubber
*Industrial products - tires and tubes *General rubber goods (GRG) -rubber boots *Manufacturing -belts, matting,flooring *Textile applications -rubber fiber
9
Biodegradable plastics
Decompose in natural aerobic and anaerobic environments Metabolism by microorganisms Two forms of biodegradable plastics -injection molded, films
10
Disposing of Non-degradable plastics
*Problems raising: - vegetation - blighting heritage areas - blocking drains - destroying natural habitat *Problems solving - mixing dirty polymers - crafts with plastic bags - replace by degradable plastic products
11
Degradable Plastics 1. biopolymers 2. synthetic biodegradable plastics
The Three important categories: 1. biopolymers 2. synthetic biodegradable plastics 3. photodegradable plastics
12
Biopolymers *Input materials: renewable or synthetic *Four main bases:
-sugar, starch, cellulose, synthetic materials (petroleum) *Functional group to show biodegradability - ester bonds *Example: Polyhydroxyalkanoates
13
Polyhydroxyalkanoates (PHAs)
*Naturally occuring form of polyester *More than a hundred PHA polymers *Two examples: -Polyhydroxybutyric ( PHB ) -Polyhydroxyoctanoate ( PHO )
14
Example of PHAs: PHB *Produced by microorganisms - Ralstonia Eutrophus, Bacillus Megaterium *Stiff, highly crystalline polymer *Limitation in the production - brittleness - high cost *Uses - packaging -beverage containers
15
Synthetic Biodegradable Plastics
By synthetic biodegradable polymer Funtional groups: esters, anhydrides, orthoesters, amides,etc Synthesized by ring opening polymerization
16
Biodegradable polymers
*Polyanhydrides -functional group: anhydride group -by melt condensation polymerization -uses: short-term release of drugs, bioactive agent, controlled drug delivery devices.
17
Biodegradable polymers
Graft polymers -funtional group: carbonyl group -form by amino acid halide and polymers with carbonyl group -uses: medical issues
18
Decomposition of Biodegradable polymers by microbes
Break down into simpler compound Aerobic conditions - consume oxygen - into carbon dioxide and water Anaerobic conditions -do not consume oxygen - into methane and carbon dioxide
19
Advantages of using biodegradable polymers
Reduce the disposal of non-degradable products Reduce the cost of building up landfills Reduce the problems of toxicity
20
Photodegradable Plastics
Decompose when exposed to sunlight Functional group : Aromatic-based Examples: Polyvinyl Chloride, Polyamides, Polystyrene Uses: Photodegradable plastic bags
21
Limitation of Photodegradable plastics
Not easy to expose under sunlight in landfill - cover by other waste products Possible byproducts - toxic, harmful environmental problems Takes long time to decay - pose hazard to wild life - contribute to solid waste volume
22
References 1_1528.html
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.