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Polymer of low concern (PLC) criteria

A 'polymer of low concern' (PLC) is a polymer that we consider to be of low concern to human health and the environment because it meets all the criteria we have set.

Note: If you hold a current PLC certificate for a polymer that NICNAS issued, you do not need to do anything. The polymer will be listed on the Inventory when the 5 year pre-listing period expires. You cannot cancel or change your certificate after it has been issued.

If you meet the PLC criteria, your introduction is categorised as exempted. If your polymer does not meet the PLC criteria, go to our guidance to categorise your introduction as exempted, reported or assessed.

Is my polymer eligible to be introduced as a PLC?

To be eligible to be introduced as a PLC, a polymer must:

  • have a number average molecular weight ≥ 1,000 g/mol as well as meet the low molecular weight species and reactive functional group requirements

    or

  • be a polyester manufactured solely from prescribed reactants

Other criteria that must be met

To be eligible to be introduced as a PLC, a polymer must also meet the following criteria:

  • have a low cationic density
  • contain approved elements only
  • not contain any difluoromethylene or trifluoromethyl groups
  • be stable under the conditions in which it is used
  • not be a high molecular weight (≥10,000 g/mol) water absorbing polymer
  • not have any known hazard classification

Low molecular weight species requirements

Except for polyesters manufactured solely from prescribed reactants, a PLC must meet the percentage of low molecular weight species requirements. This is dependent on the number average molecular weight (NAMW) of the polymer.

For polymers with an NAMW ≥ 1,000 g/mol and < 10,000 g/mol, the allowable content of low molecular weight species is:

  • < 10% below 500 g/mol

    and

  • < 25% below 1,000 g/mol.

For polymers with an NAMW ≥ 10,000 g/mol, the allowable content of low molecular weight species is:

  • < 2% below 500 g/mol

    and

  • < 5% below 1,000 g/mol.

Note: Residual monomers and reactants aren’t included when finding the content of low molecular weight species. The low molecular weight species in a polymer refers only to the oligomer content with NAMW less than 1,000 g/mol. We define oligomers as the low molecular weight species derived from the polymerisation reaction. This definition is consistent with the US EPA’s definition in its polymer exemption criteria.

Reactive functional groups (RFG) requirements

A RFG is defined as ‘an atom, or an associated group of atoms, in an industrial chemical that is intended, or may reasonably be expected, to undergo chemical reaction’.

For polymers with an NAMW ≥ 10,000 g/mol, there is no restriction on RFGs.

For polymers with an NAMW ≥ 1,000 g/mol and < 10,000 g/mol, a PLC must meet the following RFG requirement.

Scenario Outcome
The polymer includes moderate concern RFGs and doesn’t include high concern RFGs. It must have a combined Functional Group Equivalent Weight (FGEW) of at least 1,000 g/mol, calculated based on all moderate concern RFGs present in the polymer.
The polymer includes high concern RFGs. Regardless if moderate concern RFGs are present, it must have a combined FGEW of at least 5,000 g/mol, calculated based on all moderate and high concern reactive functional groups present in the polymer.

RFG categories – low, moderate and high concern

RFGs are divided into 3 categories — low, moderate and high concern — to reflect the comparative reactivity of each functional group. The table below shows reactive functional groups and their level of concern.

Table of reactive functional group categories

Reactive functional group Concern category
Aliphatic hydroxyls Low
Blocked isocyanates (including ketoxime-blocked isocyanates) Low
Butenedioic acid groups Low
Carboxylic acids Low
Conjugated olefinic groups contained in naturally occurring fats, oils and carboxylic acids Low
Halogens (except reactive halogen-containing groups such as benzylic or allylic halides) Low
Imidazolidinone groups Low
Imides Low
Organic phosphate esters1 Low
Thiols Low
Unconjugated nitriles Low
Unconjugated olefinic groups considered ‘ordinary’2 Low
Acid anhydrides Medium
Acid halides  Medium
Aldehydes  Medium
Alkoxysilanes (with alkoxy greater than C2-alkoxysilane) Medium
Allyl ethers  Medium
Conjugated olefinic groups not contained in naturally occurring fats, oils and carboxylic acids Medium
Cyanates  Medium
Epoxides  Medium
Hemiacetals Medium
Imines (ketimines and aldimines)  Medium
Methylol-amides  Medium
Methylol-amines  Medium
Methylol-ureas Medium
Unsubstituted positions ortho or para to phenolic hydroxyl Medium
Alkoxysilanes (with alkoxy of C1-or C2- alkoxysilane) High
Alpha lactones High
Amines High
Aziridines High
Azo groups High
Beta lactones High
Carbodi-imides High
Disulfides High
Halosilanes High
Hydrazines High
Hydrosilanes High
Isocyanates High
Isothiocyanates High
Trithiocarbonates High
Vinyl sulfones High
Any other reactive functional group that is not a low or a moderate concern RFG High

1 – Must still meet the approved elements criterion to be eligible to be regulated as a PLC.

2 – Not specially activated either by being part of a larger functional group, such as a vinyl ether, or by other activation influences (for example, a strongly electron-withdrawing sulfone group with which the olefinic groups interact).

The category of the RFG is based on the presence of chemically or metabolically-reactive or toxic (including eco-toxic) functional groups within the polymer.

Low concern RFGs

RFGs in the low concern category generally: 

  • lack reactivity in biological and/or aquatic media

    or

  • have low reactivity that does not have adverse effects.

There are no restrictions for low concern functional groups. These may be used without limit.

Moderate concern RFGs

RFGs in the moderate concern category have evidence of reactivity in biological and/or aquatic media but the effects are not severe enough to place the functional group in the high concern category.

High concern RFGs

RFGs in the high concern category are the most reactive and are known to pose health and/or environmental concerns.

If there is no, insufficient or contradictory information on a RFG it defaults to the high concern category. This category applies until sufficient information becomes available to move it to another category.

Functional groups not considered to be RFGs

A number of functional groups are implicitly not considered to be RFGs. These include:

  • carboxylic esters
  • ethers
  • amides
  • urethanes
  • sulfones and
  • nitro groups.

This is provisional on the functional group not being modified to enhance its reactivity (for example, the dinitrophenyl ester of a carboxylic acid).

Polyesters

A polyester is a polymer with molecules containing at least 2 carboxylic acid ester linkages, at least 1 of which links internal monomer units together.

Polyesters manufactured solely from prescribed reactants, including any reactants at less than 2%, are eligible to be introduced as PLCs. This provision is independent of the NAMW and low molecular weight species criterion. However, all other PLC criteria must be met. Thus, certain polyesters will not be eligible to be introduced as PLCs, including: 

  • biodegradable polyesters
  • highly water-absorbing polyesters with NAMW greater than or equal to 10,000 g/mol.

A number of prescribed reactants are not on the Australian Inventory of Industrial Chemicals (the Inventory). Thus, before you manufacture polyesters from these reactants in Australia, you must first find out the introduction category for these reactants.

On the other hand, polyesters manufactured from these reactants overseas could be imported as the reactant itself would not be introduced.

Note: In addition, the methyl and ethyl ester as well as anhydride derivatives of a listed substance in the table are allowed. However no pendant anhydrides should remain in the final polyester polymer.

Table of prescribed reactants

Reactants CAS Number
Monobasic acids and natural oils
Benzoic acid 65-85-0
Canola oil 120962-03-0
Castor oil  8001-79-4 
Castor oil, dehydrated 64147-40-6
Castor oil, dehydrated, polymerised 68038-02-8
Coconut oil 8001-31-8
Coconut oil, hydrogenated 84836-98-6
Corn oil 8001-30-7
Cottonseed oil 8001-29-4
Dodecanoic acid 143-07-7
Fats and glyceridic oils, anchovy 128952-11-4
Fats and glyceridic oils, babassu 91078-92-1
Fats and glyceridic oils, herring 68153-06-0
Fats and glyceridic oils, menhaden 8002-50-4
Fats and glyceridic oils, sardine 93334-41-9
Fats and glyceridic oils, oiticica 8016-35-1
Fatty acids, C8-10 68937-75-7
Fatty acids, C14-18 and C16-18-unsaturated 67701-06-8
Fatty acids, C16-18 and C18-unsaturated 67701-08-0
Fatty acids, castor-oil 61789-44-4
Fatty acids, coco 61788-47-4
Fatty acids, corn oil 68308-50-9
Fatty acids, dehydrated castor-oil 61789-45-5
Fatty acids, linseed oil 68424-45-3
Fatty acids, olive-oil 92044-96-7
Fatty acids, safflower oil 93165-34-5
Fatty acids, soya 68308-53-2
Fatty acids, sunflower oil 84625-38-7
Fatty acids, sunflower-oil, conjugated 68953-27-5
Fatty acids, tall-oil 61790-12-3
Fatty acids, tall-oil, conjugated N/A
Fatty acids, vegetable oil 61788-66-7
Fish oil 8016-13-5
Glycerides, C16-18 and C18-unsaturated 67701-30-8
Heptanoic acid 111-14-8
Hexadecanoic acid 57-10-3
9-Hexadecenoic acid, (9Z)- 373-49-9
Hexanoic acid 142-62-1
Hexanoic acid, 3,3,5-trimethyl- 23373-12-8
Hexanoic acid, 3,5,5-trimethyl- 3302-10-1
Linseed oil 8001-26-1
Linseed oil, oxidized 68649-95-6
Linseed oil, polymerized 67746-08-1
Nonanoic acid 112-05-0
Octadecanoic acid 57-11-4
9-Octadecenoic acid (9Z) 112-80-1
9,12-Octadecadienoic acid (9Z,12Z)- 60-33-3 
Oils, cannabis N/A
Oils, palm kernel 8023-79-8
Oils, perilla 68132-21-8
Oils, walnut 8024-09-7
Olive oil 8001-25-0 
Safflower oil 8001-23-8
Soybean oil 8001-22-7
Sunflower oil 8001-21-6
Tung oil 8001-20-5 
Di and tri basic acids
1,2-Benzenedicarboxylic acid 88-99-3
1,3-Benzenedicarboxylic acid 121-91-5
1,3-Benzenedicarboxylic acid, dimethyl ester 1459-93-4
1,4-Benzenedicarboxylic acid 100-21-0
1,4-Benzenedicarboxylic acid, diethyl ester 636-09-9
1,4-Benzenedicarboxylic acid, dimethyl ester 120-61-6
1,2,4-Benzenetricarboxylic acid 528-44-9
Butanedioic acid 110-15-6
Butanedioic acid, diethyl ester 123-25-1
Butanedioic acid, dimethyl ester 106-65-0
2-Butenedioic acid (E)- 110-17-8
1,4-Cyclohexanedicarboxylic acid  1076-97-7 
Decanedioic acid 111-20-6
Decanedioic acid, diethyl ester 110-40-7
Decanedioic acid, dimethyl ester 106-79-6
Dodecanedioic acid 693-23-2
Fatty acids, C18-unsaturated, dimers 61788-89-4
2,5-Furandione, dihydro-  108-30-5
Heptanedioic acid 111-16-0
Heptanedioic acid, dimethyl ester 1732-08-7
Hexanedioic acid 124-04-9
Hexanedioic acid, diethyl ester  141-28-6
Hexanedioic acid, dimethyl ester 627-93-0
5-Isobenzofurancarboxylic acid, 1,3-dihydro-1,3-dioxo- 552-30-7
1,3-Isobenzofurandione 85-44-9
Nonanedioic acid 123-99-9
Nonanedioic acid, diethyl ester 624-17-9
Nonanedioic acid, dimethyl ester 1732-10-1
Octanedioic acid 505-48-6
Octanedioic acid, dimethyl ester 1732-09-8
Pentanedioic acid 110-94-1
Pentanedioic acid, diethyl ester 818-38-2
Pentanedioic acid, dimethyl ester 1119-40-0
Undecanedioic acid 1852-04-6
Unsaturated fatty acids, C18, dimers, hydrogenated 68783-41-5 
Polyols
1,3-Butanediol 107-88-0
1,4-Butanediol 110-63-4
1,4-Cyclohexanedimethanol 105-08-8
1,2-Ethanediol 107-21-1
Ethanol, 2,2´-oxybis- 111-46-6
1,6-Hexanediol 629-11-8
1,3-Pentanediol, 2,2,4-trimethyl- 144-19-4
1,2-Propanediol 57-55-6 
1,3-Propanediol  504-63-2
1,3-Propanediol, 2,2-bis(hydroxymethyl)- 115-77-5
1,3-Propanediol, 2,2-dimethyl- 126-30-7
1,3-Propanediol, 2-ethyl-2-(hydroxymethyl)- 77-99-6
1,3-Propanediol, 2-(hydroxymethyl)-2-methyl- 77-85-0
1,3-Propanediol, 2-methyl- 2163-42-0
1,2,3-Propanetriol 56-81-5
1,2,3-Propanetriol, homopolymer 25618-55-7
2-Propen-1-ol, polymer with ethenylbenzene 25119-62-4
Modifiers
Acetic acid, 2,2´-oxybis- 110-99-6
1-Butanol (1-Butanol may not be used in a substance manufactured from fumaric or maleic acid because of potential risks associated with esters which may be formed by reaction of these reactants.) 71-36-3
Cyclohexanol 108-93-0
Cyclohexanol, 4,4´-(1-methylethylidene)-bis- 80-04-6
Ethanol  64-17-5
Ethanol, 2-(2-butoxyethoxy)- 112-34-5
1-Hexanol 111-27-3
Methanol 67-56-1 
Methanol, hydrolysis products with trichlorohexylsilane and trichlorophenylsilane 72318-84-4
1-Phenanthrenemethanol, tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)- 13393-93-6
Phenol, 4,4´-(1-methylethylidene)bis-, polymer with 2,2´-[(1-methylethylidene)bis(4,1-phenyleneoxymethylene)]bis[oxirane] 25036-25-3 
1-Propanol, 2-methyl-  78-83-1
1-Propanol, 2-methyl- 
Siloxanes and Silicones, dimethyl, diphenyl, polymers with phenyl silsesquioxanes, methoxy-terminated
68440-65-3
Siloxanes and Silicones, dimethyl, methoxy phenyl, polymers with phenyl silsesquioxanes, methoxy-terminated 68957-04-0
Siloxanes and Silicones, methyl phenyl, methoxy phenyl, polymers with phenyl silsesquioxanes, methoxy- and phenyl-terminated 68957-06-2
Silsesquioxanes, phenyl propyl 68037-90-1

Other criteria

To be introduced as a PLC, a polymer must also meet the criteria for:

  • low cationic density
  • approved elements
  • difluoromethylene or trifluoromethyl groups
  • stability
  • water absorption
  • known hazard classification

Low cationic density

Cationic polymers and polymers likely to become cationic in a natural aquatic environment are not eligible to be introduced as PLCs. The main concern is their toxicity towards aquatic organisms such as fish and algae.

A polymer is a low cationic density polymer if it is: 

  • not a cationic polymer or is not likely to become a cationic polymer in a natural aquatic environment (4<pH<9)
  • not soluble (< 0.1 mg/L) or dispersible in water and will only be used in solid phase (for example ion exchange beads), or 
  • cationic (or potentially cationic) and the combined (total) FGEW of cationic groups is at least 5,000 g/mol. 

A cationic polymer is a polymer containing a net positively-charged atom/s or associated group/s of atoms covalently linked to its polymer molecule. Examples are the ammonium, phosphonium and sulfonium cations.

A potentially cationic polymer is a polymer containing groups likely to become cationic. Examples are all: 

  • amines (for example primary, secondary, tertiary and aromatic)
  • isocyanates (which hydrolyse to form carbamic acids, then decarboxylate to form amines).

Example of low charge density

Consider a polyamide with a NAMW 7,000 g/mol manufactured from equimolar amounts of ethylenediamine and isophthalic acid. On average, the polymer will have 1 unreacted amino group at 1 end of the polymer chain and an unreacted carboxylic acid group at the other end. As the amino group is potentially cationic, it needs to be included in the calculation of the FGEW  of cationic groups in this polymer. The FGEW for the amino group can be calculated by end-group analysis, that is 7,000/1 g/mol. Therefore, the polymer meets the criteria for low cationic density as the FGEW is above 5,000 g/mol. If the NAMW had been less than 5,000 g/mol, or if the polymer had 2 free amine groups, then the polymer would not be eligible to be introduced as a PLC.

Note: There is no high NAMW cut-off for cationic density. Thus, even if a polymer has a NAMW of ≥ 10,000 g/mol it still needs to have a FGEW of cationic groups of 5,000 g/mol or above, or it will not meet the PLC criteria.

Approved elements

A PLC must contain, as an integral part of its composition, at least 2 of the atomic elements carbon, hydrogen, nitrogen, oxygen, silicon and sulfur.

Excluding impurities, a PLC must only contain the following:

  • carbon, hydrogen, nitrogen, oxygen, silicon and sulfur
  • sodium, magnesium, aluminium, potassium, calcium, chlorine, bromine and iodine as the monatomic counter-ions Na+, Mg2+, Al3+, K+, Ca2+, Cl-, Br- or I-
  • fluorine, chlorine, bromine or iodine covalently bound to carbon
  • less than 0.2% (by weight) of any combination of the atomic elements (boron, copper, iron, lithium, manganese, nickel, phosphorus, tin, titanium, zinc and zirconium).

No other elements are allowed, except as impurities. Specifically, the fluoride anion (F-) is not allowed as it has a high acute toxicity.

This requirement refers to monatomic species only. For example, a polymer containing the ammonium counter ion (NH4+) may be a PLC provided it meets the other PLC criteria.

With the binding of halogens to carbon, note that we wouldn’t allow the perchlorate anion ClO4- because the chlorine is not covalently bound to carbon, but we would allow the trichloroacetate anion CCl3CO2-.

Difluoromethylene or trifluoromethyl groups

A polymer is not eligible to be a PLC if it contains any difluoromethylene (CF2) or trifluoromethyl (CF3) groups.

The primary concern for such fluorinated polymers is degradation in the environment to release potentially persistent, bioaccumulative or toxic degradation products.

Stability

A PLC must be a stable polymer.

A polymer is not eligible to be introduced as a PLC if it substantially degrades, decomposes or depolymerises during use. That is, the polymer is considerably, meaningfully or to a significantly large extent changed into simpler, smaller weight chemicals as the result of, but not limited to: 

  • oxidation
  • hydrolysis
  • heat
  • sunlight
  • attack by solvents or
  • microbial action.

Examples of polymers that would not meet this criterion include those that are:

  • designed to be pyrolysed or burnt
  • designed or likely to substantially photodegrade
  • explosive
  • designed or likely to substantially biodegrade (for example, starch)
  • hydrolytically unstable (t1/2 < 12 hours).

Note: A polymer may still be eligible as a PLC despite its potential to substantially degrade in the environment if the polymer is protected from degradation by being encapsulated during use. For example, polymers used in coatings, cements, adhesives, hot melts, and extrusion molding would be eligible as a PLC. In those situations, the polymer would be expected to be protected from environmental degradation.

Water absorption

Polymers with NAMW greater than or equal to 10,000 g/mol that are water absorbing (meaning a polymer capable of absorbing its own weight in water) do not qualify to be introduced as PLCs. A water absorbing polymer is capable of absorbing its own weight in water.

This criterion is for water absorbing polymers in particulate form only. It’s directed towards polymers known as 'super absorbents', such as those used in disposable nappies and paper towels.

We’ve based our concerns for water absorbing polymers on a 2-year inhalation study in rats using a high molecular weight water-absorbing polyacrylate polymer. The study data included observations of cancer in the rats.

We don’t consider water-soluble and water dispersible polymers to be water absorbing. This is because we assume that the normal clearance mechanisms of lungs after inhalation adequately clears particles of these polymers.

Known hazard classification

A polymer can only be a PLC if it does not have any known hazard classification. We’ve prepared guidance on hazardous industrial chemicals.

How to calculate functional group equivalent weight (FGEW)

The FGEW is used to determine if the RFGs in a polymer are substantially diluted by polymeric material to allow the polymer to be introduced as a PLC.

The FGEW of a polymer is the ratio of the NAMW to the number of functional groups in the polymer. It’s the weight of a polymer that contains 1 formula weight of the functional group.

We don’t restrict the level of low concern RFGs in the polymer. We permit low concentrations of moderate and high concern RFGs in polymer molecules, but the reactivity of the functional group/s in question restricts the quantity.

Unless the FGEW can be determined empirically by recognised, scientific methodology (typically titration), a worst-case estimate must be made for the FGEW.

All moderate and high concern functional groups must be taken into account when calculating FGEW.

End-group analysis or percent charged method

The FGEW may be calculated by end-group analysis or by the percent charged method.

End-group analysis applies to polymers containing reactive functional groups at terminal positions.

The percent charged method applies to polymers with reactive functional groups distributed throughout the polymer.

End group analysis – linear and branched polymers

FGEW example equations 1 (linear) and 2 (branched)

Linear polymers

For linear polymers containing RFGs only at the terminal positions, the FGEW can be calculated using equation 1.

A mathematical equation showing how to calculate functional group equivalent weight for a linear polymer.

Equation 1 – linear polymers

For linear polymers, such as some condensation polymers (for example, polyesters and polyamides), the only RFGs are at the end of the chain because the others are used up in the condensation reaction. The number of end groups (n) may be equal to 1 or 2 depending on the molar ratio of the starting monomers.

For example, for a polyamide with a NAMW 1,500 g/mol made from an excess of ethylenediamine and adipic acid, an amine group (high concern) would be expected at each end of the polymer chain. Therefore, the amine FGEW = 1,500/2 = 750 g/mol.

On the other hand, if the polyamide was made from equimolar amounts of ethylenediamine and adipic acid, the polymer will on average have 1 unreacted amine group at 1 end of the polymer chain and an unreacted carboxylic acid group at the other end. In this case, the amine FGEW = 1,500/1 = 1,500 g/mol (the carboxylic acid group is not considered in the calculation, as it is a low concern RFG).

In both examples, the polymer would not be eligible to be introduced as a PLC as the amine FGEW is below the required minimum equivalent weight threshold of 5,000 g/mol for polymers containing high concern (potentially cationic) groups.

Branched polymers

For simple branched polymers (having only 1 monomer possessing more than 2 reactive sites), the FGEW is calculated from an estimated degree of branching. This is derived by knowing the number of reactive groups in the polyfunctional monomer. It’s assumed that the monomer responsible for the branching will be incorporated in its entirety to form the polymer. The FGEW can be calculated using equation 2.

A mathematical equation showing how to calculate functional group equivalent weight for a branched polymer.

Equation 2 – branched polymers

Consider a branched polyurethane polymer containing isocyanate groups (high concern) at chain ends derived from the polymerisation of pentaerythritol (molecular weight (MW) 136 g/mol) with polypropylene glycol and an excess of isophorone diisocyanate. The polyfunctional branching monomer pentaerythritol (4 reactive sites) is added to the reaction at 10 weight %. The NAMW of the polymer is 2,720 g/mol.

The chemical structure of a branched polyurethane polymer.
An example FGEW calculation for a branched polyurethane polymer.

 

In the above example, the polymer would not be eligible to be introduced as a PLC as the isocyanate FGEW is below the required minimum equivalent weight threshold of 5000 g/mol for polymers containing high concern groups.

Percent charged method

Some condensation and addition reactions create polymers where not all RFGs along the backbone of the polymer are consumed during the reaction, so an accurate FGEW cannot be determined through a simple end-group analysis. For any of these polymers, FGEW can be calculated according to equation 3.

A mathematical equation showing how to calculate functional group equivalent weight for a polymer using the percent charged method.

Equation 3 – percent charged method

For example, for an acrylic polymer containing 7.5 weight % acryloyl chloride monomer (MW 90.5 g/mol), the FGEW of acid chloride groups in the polymer is:

An example FGEW calculation, using the percent charged method, for a polymer.

Combined FGEW calculation for multiple RFGs in a polymer

If the various RFGs in a polymer arise from multiple monomers, the FGEW must be calculated for each monomer separately, and then the combined FGEW is calculated according to equation 4.

A mathematical equation showing how to calculate combined functional group equivalent weight for a polymer with multiple reactive functional groups.

Equation 4 – combined FGEW calculation for multiple RFGs in a polymer

FGEW calculation examples

Example 1

Consider the reaction between ethylenediamine (MW 60 g/mol) (charged at 30 weight %) and diglycidyl ether (MW 130 g/mol) (charged at 70 weight %) to give a polymer of NAMW of 5,000 g/mol. The epoxides in the backbone are reacted to give an aliphatic alcohol (low concern). The amine groups remain intact, with their FGEW proportional to the charged amount of ethylenediamine. As the diglycidyl ether is in excess, it can be assumed that the polymer is epoxide-terminated at both ends.

The chemical structure of a polymer formed by reacting ethylenediamine and diglycidyl ether.

Using equation 3, the FGEW for the amine group (high concern) is (100 x 60)/(30 x 2) = 100 g/mol. The FGEW for the epoxide group (moderate concern) can be calculated using end group analysis (equation 1), that is, 5,000/2 = 2,500 g/mol.

Then, using equation 4, FGEWcomb = inverse of [1/100 + 1/2500] = 96 g/mol.

In this example, the polymer would not be eligible as a PLC.

Example 2

Consider a p-cresol-formaldehyde condensation polymer which is reacted with 1.5 weight % epichlorohydrin to give an epoxide-capped resin. As a worst-case scenario, it is assumed that the polymer is phenol-terminated. This would mean phenol groups with reactive ortho positions reside at the polymer backbone termini. The polymer also contains epoxy rings from the epichlorohydrin (MW 92.5 g/mol). Both reactive functional groups are moderate concern. A NAMW of 8,000 g/mol is assumed.

The chemical structure of a p-cresol-formaldehyde condensation polymer.

Using equation 3, the FGEW for the epoxide group is (100 × 92.5)/(1.5 × 1) = 6,167 g/mol. The FGEW for the phenol group can be calculated using end group analysis (equation 1), that is, 8,000/2 = 4,000 g/mol.

Then, using equation 4, FGEWcomb = inverse of [1/6,167 + 1/4,000] = 2,426.

With a combined FGEW of 2,426 g/mol, this polymer would be eligible to be introduced as a PLC because the FGEWcomb is above the required minimum equivalent weight threshold of 1,000 g/mol for a polymer containing moderate concern functional groups.

Example 3

Consider the addition reaction involving the polymerisation of three acrylates, glycidyl methacrylate (10 weight %, MW 142 g/mol, 1 RFG), hydroxymethyl acrylamide (2 weight %, MW 101 g/mol, 1 RFG) and acrylic acid (88 weight %).

In this case, it can be assumed that each monomer is completely incorporated into the polymer, with the RFGs of concern being the epoxide group (moderate concern) from glycidyl methacrylate and the hydroxymethyl amide group (moderate concern) from the acrylamide. The carboxylic acid moiety from acrylic acid is of low concern and need not be included in FGEW calculations.

The chemical structure of a polymer formed by polymerisation of 3 acrylates.

Using equation 3, the FGEW for the epoxide group is (100 × 142)/(10 × 1) = 1,420 g/mol. Again using equation 3, the FGEW for the hydroxymethyl amide group is (100 × 101)/(2 × 1) = 5,050 g/mol.

Then, using equation 4, FGEWcomb = inverse of [1/1,420 + 1/5,050] = 1,108 g/mol.

With a combined FGEW of 1,108 g/mol, this polymer would be eligible to be introduced as a PLC because the FGEWcomb is above the required minimum equivalent weight threshold of 1,000 g/mol for a polymer containing moderate concern functional groups.

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