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8/2/2019 Flame Retardant Pp http://slidepdf.com/reader/full/flame-retardant-pp 1/22 By Harshini Tammareddy 09120018

Flame Retardant Pp

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Page 1: Flame Retardant Pp

8/2/2019 Flame Retardant Pp

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ByHarshini Tammareddy

09120018

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Polypropylene was the first synthetic stereo-

regular polymer to achieve industrial

importance and it is presently the fastest

growing fibre for technical end-uses. Polypropylene fibres have been widely used

in apparel, upholstery, floor coverings,

hygiene medical, geotextiles, car industry,

automotive textiles, various home textiles,wall-coverings and so on .

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The crystalline melting point of isotacticpolypropylene with a crystallinity of around45% and containing 90–95% isotactic materialis quoted as 165 °C.

Because of its wholly aliphatic hydrocarbonstructure, polypropylene by itself burns veryrapidly with a relatively smoke-free flameand without leaving a char residue. It has a

high self-ignition temperature (570 °C) and arapid decomposition rate compared withwood and other cellulosic materials andhence has a high flammability.

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While polypropylene fibres may be treated

with flame retardant finishes and back-

coatings in textile form with varying and

limited success, the ideal flame retardantsolution for achieving fibres with good

overall performance demands that the

property is inherent within the fibre.

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By inhibiting the initiating radicals in the pre-flame andflame zones; typically, antimony–halogen based

additives are effective here; By adding some hydrated inorganic additives which

decompose endothermically and release water, andhence withdraw heat from the substrate and dilute thecombustible volatiles;

By modifying the chemical structure of the polymer tochange its decomposition procedure and/or to improvethe compatibility with other flame retardants;

By addition of char-forming additives preferably having

an intumescent property.

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Most flame retardants act either in the

vapour phase or the condensed phase

through a chemical and/or physical

mechanism to interfere with the combustionprocess during heating, pyrolysis, ignition or

flame spread stages

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There are two main types of flame retardants

for polypropylene: namely the additive and

the reactive types.

Additive type flame retardants, generallyincorporated into the polymer by physical

means, have been widely used and include

many of the commonly used antimony–

bromine, intumescent and hydrated fillerformulations available

Disadvantage :Poor compatibility, leaching,

and a reduction in mechanical properties.

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Reactive flame retardants : Involves either thedesign of new, intrinsically flame-retardingpolymers or modification of existing polymersthrough copolymerisation with a flame-retarding

unit either in the chain or as a pendant group. Inthis the incorporation of even a few weightpercent of the unit into the polymer chains canlead to remarkable improvements in the overallflame retardency of the polymer .

Disadvantages :This lacks sufficient versatility inmanufacturing, processing and is uneconomical,due to the expense associated with developing anew material for use.

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Five principal types of generic flame retardant

systems for inclusion in polypropylene fibers

have been identified .

1. phosphorus-containing

2. halogen-containing

3. silicon-containing

4. metal hydroxide and oxide and5. Nanocomposite flame retardant formulations.

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The range of phosphorus-containing flame

retardants is extremely wide since the

element exists in several oxidation states.

Phosphines, phosphine oxides, phosphoniumcompounds, phosphonates, elemental red

phosphorus, phosphites and phosphate are all

used as flame retardants in polymers in

general, although, only few of these are

applicable to polyolefins and especially

polypropylene.

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Ammonium polyphosphate (APP) is a very

commonly used flame retardant in PP often

combined with cyclic urea–formaldehyde

resins, hydroxyethylcyanuarates orpiperazine-base species which usually

demonstrate phosphorus–nitrogen synergism.

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Phosphorus-containing species typically act

in the condensed phase promoting char

formation on the surface initially, which

functions as a barrier to inhibit furtherdegradation and hence starve the flame of 

fuel and protect the polymer surface from

heat and air.

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Halogen-containing species, often in

combination with some phosphorus and

antimony-containing flame retardants,

usually act in the vapour phase by capturingthe radicals to interrupt the exothermic

oxidative flame chemical processes and thus

suppress combustion.

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Considerable research has shown that theaddition of relatively small amounts of silicon compounds, especially when added tointumescent formulations to pp can

significantly improve their flame retardency,through both char formation in thecondensed phase and the trapping of activeradicals in the vapour phase. Silicone-

containing flame retardants are consideredto be ‘environmentally friendly’ additivesbecause their use is claimed to lead to areduction in the harmful impact onenvironment

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Other advantages of the silicone-based

additives are that they can improve the

impact resistance dramatically and add the

conventional silicone properties of improved

mouldability , processibility , gloss and

electric insulating properties

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Solid phase reaction.

The incorporation of silicones often produces

slight intumescent char formation in

polypropylene, while the polymer itself burnswithout a char .

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The main interest for metal hydroxide flame

retardants for polypropylene lies in their low

toxicity, corrosion properties and emission of 

smoke during processing and burning.

These compounds offer an attractive

alternative to halogenated formulations for

flame-retarding polypropylene. These metal

hydroxides decompose endothermically andrelease water during burning and thus reduce

the heat and temperature from the substrate

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However, very high metal hydroxide

concentrations are usually required to

achieve an acceptable degree of flame

retardancy and tend to be poor in

mechanical strength .

Typical metal hydroxide flame retardants are

Al(OH)3 and Mg(OH)2.

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During the last six years or so, nanocompositeshave been considered to be a new class of flameretardant system for polymers.

In particular, organic–inorganic nanocomposites,

comprising organically modified clay dispersed inselected polymer matrices have attractedconsiderable attention with the advantage thatthey are efficient at concentrations of 5% w/wor less . Several kinds of nanocompounds can be

used to enhance the flame retardancy of polymers in general and polypropylenespecifically, such as modified montmorillonites ,TiO2, Sb2O3 and boroxosiloxanes .

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Typical nanocomposites are usually prepared

by a blending process or by bulk

polymerisation and they may exist in either

an intercalated form, in which interlaminar

contact is maintained between the

aluminosilicate layers, or in an exfoliated

form, in which such registry is lost and the

layers are completely delaminated by the

incoming material and hence result with the

silicate layers fully dispersed throughout the

matrix

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Building/Construction applications as pipes,

lamp holders, stadium seats, fiber spinning

etc.

Temperature resistant tubes,pipes, etc. Textile industry.

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