POLYMER SCIENCE AND TECHNOLOGY

Slides:



Advertisements
Similar presentations
Polyester or polyamide …….. you decide!! (1) nylon - 6,10.
Advertisements

Polymerization kinetics
Polymerization reactions chapter 4. Fall outline Introduction Classifications Chain Polymerization (free radical initiation) Reaction Mechanism.
Importance of Functional Groups in the Synthesis of Polymers Indicators C-3.5 and C-3.7 South Carolina Science Standards Chemistry Section.
Aim: Why do organic reactions occur more slowly than inorganic reactions? Combustion- Hydrocarbons (HC’s) will burn with sufficient amount of oxygen to.
Types of Vinyl Polymerization MethodAdvantagesDisadvantages Bulk (Neat)Simple equipment Rapid reaction Pure polymer isolated Heat buildup Gel effect Branched.
Synthetic Polymers. Introduction A polymer is a large molecule composed of many smaller repeating units. First synthetic polymers:  Polyvinyl chloride.
Outline:1/19/07 n n Pick up Quiz #1 – from me n n Chem Seminar: 4pm n n Chapter 13 (cont’d) Macromolecules.
Chemistry 367L/392N Paul J Flory Macromolecular Chemistry Wallace H. Carothers
Chemistry 367L/392N Macromolecular Chemistry Step Growth Chain Growth Lecture 5.
Polymerization reactions chapter 4. Fall outline Introduction Classifications Chain Polymerization (free radical initiation) Reaction Mechanism.
- Organic Reactions Mr. ShieldsRegents Chemistry U17 L03.
CLASSIFICATION OF POLYMERIZATION REACTIONS For polymerization it is required that the monomer molecule is capable of being linked to two (or more) other.
Synthetic and Biological Polymers
Polymerization Reactions
POLYMERS.
Macromolecule s K Warne. C H H C H H C H H C H H C H H C H H C H H C H H Macromolecules What do you notice about this structure? It is made of lots of.
Alcohols, Acids, Esters R – OH R – COOH R – COOR1.
Unit 31 - Organic Functional Groups and Introduction to Polymers.
PETROLEUM AS A BUILDING SOURCE Petrochemicals- from oil/nat.gas Detergents, plastics, drugs, fabrics, cosmetics, rubber, etc. Few molecules needed to build.
Ionic Polymerization.
Chapter 4 Step-Reaction polymerization Chemical and Bioengineering Konkuk University Oct. 10,
Christian Brothers High School Department of Chemistry Organic Chemistry II.
Polymerization Reactions Chemistry II. Types of Polymerization Reactions Addition polymerization – monomers are added together, with no other products.
Lecture 4 & 5 Polymerization Reactions Polymer Science and Engineering.
Chain and Step Growth Polymerization Brazel & Rosen 8.1
1 Polymerization kinetics of chain growth polymerization Brazel & Rosen Initiation (2 mechanisms) Propagation Termination (2 mechanisms)
Polymers are large molecules made by linking together many smaller molecules, called monomers. Polymerization reactions can either be classified as addition.
CHAIN POLYMERIZATION Free Radical Polymerization Free radical are independently-existing species that have unpaired electron. Normally they are highly.
There are two main kinds of polymers. Type 1: Addition Polymers Each small molecule adds to the end of a growing chain. Polyethylene is an example Type.
POLYMER CHEMISTRY.
Polymers are large molecules made by linking together many smaller molecules, called monomers. monomer symbol n Natural polymers include proteins, carbohydrates.
Chapter 10 Radical Reactions
PLEASE NOTE: For the exam you need to be able to describe what the steps: Initiation, propagation and termination mean and put them in order (see next.
Section 20.4 Additional Organic Compounds 1.To learn about aldehydes and ketones 2.To learn to name aldehydes and ketones 3.To learn about some common.
Polymerization Reactions Plastics, Fibers and Foods.
Single and Double Bonds
Polymerization Reactions
Organic Chemistry Chapter 22. Hydrocarbons Alkanes Saturated  Relatively unreactive due to the strong C-C and C-H bonds  Contains all C-C single bonds.
This is the page devoted to a little introduction of how polymers are made. A chemical reaction which make polymers is called a polymerization. There are.
POLYMERIZATION REACTIONS
Ionic Polymerization.
In cationic vinyl polymerization, the initiator is a cation (ion with a positive electrical charge). Mechanism A pair of electrons, negatively charged,
By: Muhammad Haseeb Iqbal National Textile University
for example: here is the monomer of polyethylene
CLASSIFICATION OF POLYMERIZATION REACTIONS
Synthetic Polymers.
BY: MAKAYLA, JONATHAN AND COURTNEY
Polymers ( Session 41 ).
23.2 Explosions Thermal explosion: a very rapid reaction arising from a rapid increase of reaction rate with increasing temperature. Chain-branching.
POLYMERS CONTENTS Prior knowledge Types of polymerisation
Aim: Why do organic reactions occur more slowly than inorganic reactions? Combustion- Hydrocarbons (HC’s) will burn with sufficient amount of oxygen to.
CHAPTER 4 Classification based on mode of formation- chain growth and step growth polymerization week 12.
Organic Chemicals Alcohols R-OH CH3OH methanol (methyl alcohol)
Engineering Materials Polymeric materials
Polymers are large molecules made up of repeating units called Monomers
Polymer chemistry: classification based on mode of formation- adition and condenzation polymerization.
Carbon Chemistry Carbon is unusual
CHM 585 / 490 Chapter 5.
Polymers.
POLYMERS.
23.2 Explosions Thermal explosion: a very rapid reaction arising from a rapid increase of reaction rate with increasing temperature. Chain-branching.
Polymers and Polymerization
Polymerization Reactions
Organic Chemicals Alcohols R-OH CH3OH methanol (methyl alcohol)
Organic Chemicals Alcohols R-OH CH3OH methanol (methyl alcohol)
Polymers!.
Adhesives and Adhesion
Created by C. Ippolito July 2007
Polymerization Reactions
Presentation transcript:

POLYMER SCIENCE AND TECHNOLOGY Polymerization Mechanism of chain growth

Reactions of polymerization are classified according to: - media of polymerization - mechanism of chain growth Media of polymerization: - homogeneous in bulk in solution - heterogeneous in bulk, in solution in suspension, in emulsion in gas phase interfacial polycondensations

Mechanism of chain growth RADICAL POLYMERIZATION a STEP BY STEP POLYMERIZATION

Mechanism of chain growth (type of reaction) 1. free-radical polymerization (addition polymerization, chain-growth of polymer) I. initiation II. propagation III. termination 2. step by step polymerization (condensation polymerization, stepwise growth of polymer) monomer + monomer → dimer dimer + monomer → trimer dimer + dimer → tetramer trimer + monomer → tetramer etc.

1. FREE-RADICAL POLYMERIZATION

ethylene polyethylene

styrene polystyrene (vinyl-benzene)

Free-radical polymerization Three phases: I. initiation II. propagation III. termination 1. Initiation – initiator decomposition Primary active species

a) inorganic initiators hydrogen peroxide, H2O2 (O-O bond) hydroxyl radical potassium persulfate, K2S2O8 (O-O bond) KO S O OK 40 2O + 2K o C sulfate anion radical

benzoyl peroxide, DBP (O-O bond) b) Organic peroxides benzoyl peroxide, DBP (O-O bond) benzoyloxy radical Di-tert-butyl peroxide (O-O bond) t-butyloxy radical

t-butylhydroperoxide (O-O bond) c) initiators with S-S bond Tetramethylthiuram disulfide , TMTD - vulcanization (CH 3 ) 2 N C S N (CH 60 o +

d) Initiators with N-N bond ,'-azobisisobutyronitrile, AIBN CH 3 C H 40 2 H o N + 2 2-cyano-2-propyl radical

The example of free-radical polymerization: ethylene polymerization 1. Initiation

2. Propagation 3. Termination – the end of polymerization a) combination

b) disproportionation c) chain transfer I- Initiator, - radical, M - monomer, kd – constant of dissociation ki- constant of initiation, kp- constant of propagation, ktk- constant of transfer with combination, ktd- constant of disproportionation, ktt- constant of chain transfer

a) combination

b) disproportionation terminated polymer chain Double bond can be attacked by radical - new polymerization starts

c) chain transfer – transfer of polymerization reaction to „something else” in a recation mixture – in general, it is not favorable type of termination RH may be initiator solvent monomer polymer

Chain transfer with initiator Initiator forms the first radicals, then attacks monomer and forms further radicals. Chain transfer with monomer rarely happens - the added quantity of initiator is very small (0,1%). At the end of polymerization there is no initiator.

Chain transfer with solvent Solvent is always present except at polymerization in bulk. Aldehides and ketones solvents are very good chain transfers because of easy discharge of H-atom.

benzene ethylbenzene toluene better chain transfer

cumene tri phenylmethane better chain transfer

Chain transfer with monomer Chain transfer with monomer rarely happens, because at the and of polymerization there is no monomer any more. Very reactive monomer is vinyl-acetate

Chain transfer with polymer It is most common chain transfer, because at the end of polymerization there are only solvent and polymer. Example: reactivity of poly(vinyl-acetate)

During a free radical polymerization there is always a possibility for polymer branching. Example: polyacrylate with high constant of chain transfer - the result is crosslinked polymer

very interesting polyethylene chain transfer: chain reacts with its own chain – intramolecular bonding This reaction is called «backbiting» - it means “to bite its own tail”.

STEP BY STEP POLYMERIZATION condenzation polymerization the product of the reaction are polymers and „little” molecules (water, ammonia, CO2 ,HCl, N2, methanol)

Step by step polymerization condensation polymerization stepwise growth of polymer monomer + monomer → dimer dimer + monomer → trimer dimer + dimer → tetramer trimer + monomer → tetramer etc. The product is polycondenzate

Step by step polymerization: 2 types 1 Step by step polymerization: 2 types 1. Two different polyfunctional monomers - every monomer has only one type of functional group: n H2N-R-NH2 + n HOOC-R'-COOH   HN-R-NH-OC-R'-COn +n H2O or generally: n A-A + n B-B  A-A-B-Bn

poly(ethylene-terephthalate), PET Example: polyester (PET) n HOCH2CH2OH + n HOOC COOH ↔ monomer ethylene glycol (EG) monomer terephthalic acid (TPA) ↔ OOC COOCH2CH2n + 2n H2O poly(ethylene-terephthalate), PET

poly(ethylene-terephthalate)PET Production of PET 1. Direct esterification n HOCH2CH2OH + n HOOC COOH ↔ monomer ethylene glycol (EG) monomer terephthalic acid (TPA) ↔ OOC COOCH2CH2n + 2n H2O poly(ethylene-terephthalate)PET

2. Ester exchange 1. H3COOC COOCH3 + HOCH2CH2OH ↔ monomer monomer dimethyl-terephthalate (DMT) ethylene-glycol (EG) ↔ HOCH2CH2OOC COOCH3 + CH3OH methyl-2-hydroxyethyl-terephthalate (MHET) methanol (M) 2. HOCH2CH2OOC COOCH3 + HOCH2CH2OH ↔ methyl-2-hydroxyethyl-terephthalate (MHET) ethylene-glycol (EG) ↔ HOCH2CH2OOC COOCH2CH2OH + CH3OH monomer 1,4-bis-hydroxyethyleneterephthalate (BHET) methanol (M)

PET 3. HOCH2CH2OOC COOCH2CH2OH ↔ monomer 1,4- 1,4-bis-hydroxyethyleneterephthalate (BHET) ↔ - OOC- -COOCH2CH2- + HOCH2CH2OH (6) ethylene-glycol (EG) PET

2. One monomer with two types of functional groups: n H2N-R-COOH   HN-R-CO n +n H2O or generally: n AB   A-B n Example: polyamide w-aminohexaacid nylon 6, perlon - polyamide