Rubber101

Glossary

Course

149 terms shown.

1. What Rubber Is

Monomer
The small molecule linked repeatedly to build a polymer.

1. What Rubber Is

Polymer
A large molecule made of many repeating monomer units.

1. What Rubber Is

Homopolymer / copolymer / terpolymer
A polymer made from one, two, or three different monomers.

1. What Rubber Is

Repeat unit
The section of chain that repeats along the polymer.

1. What Rubber Is

Degree of polymerization
The number of times the repeat unit repeats in a chain.

1. What Rubber Is

Elastomer
A polymer that recovers quickly and forcibly from large deformation.

1. What Rubber Is

Crosslink
A chemical bond joining two polymer chains, formed during vulcanization.

1. What Rubber Is

Compound
The complete mixture: base polymer plus filler, oil, protective chemicals, and cure system.

1. What Rubber Is

phr
Parts per hundred rubber. The elastomer totals 100 and all other ingredients are relative to it.

1. What Rubber Is

Thermoset
A crosslinked material that cannot be melted and reformed.

1. What Rubber Is

Thermoplastic
A material that softens on heating and hardens on cooling, repeatedly.

1. What Rubber Is

Thermoplastic elastomer (TPE)
Rubber-like behaviour from hard physical domains rather than chemical crosslinks, so it can be reprocessed.

1. What Rubber Is

Mn (number average MW)
Average molecular weight counting every molecule equally.

1. What Rubber Is

Mw (weight average MW)
Average molecular weight weighted toward larger molecules.

1. What Rubber Is

MWD (Mw/Mn)
Molecular weight distribution. Broad processes more easily; narrow performs better but is harder to process.

1. What Rubber Is

Tg (glass transition temperature)
The range below which chain motion stops and the rubber stiffens. Sets the low-temperature limit.

1. What Rubber Is

Unsaturation
Carbon-carbon double bonds in the chain. The sites sulfur uses to cure and ozone uses to attack.

1. What Rubber Is

Saturated
Containing no carbon-carbon double bonds. Requires peroxide cure but resists ozone.

1. What Rubber Is

Cis / trans
Geometry about a double bond. cis-1,4-polyisoprene is natural rubber; the trans form is a hard thermoplastic.

1. What Rubber Is

Mooney viscosity
A standard measure of raw polymer or compound viscosity, reported as ML(1+4) at a stated temperature.

1. What Rubber Is

Entanglement
Physical looping of long chains around each other; what lets chain segments carry load between crosslinks.

1. What Rubber Is

Hysteresis
Energy lost as heat each time a compound is deformed and released.

1. What Rubber Is

Viscoelasticity
Behaving partly as an elastic solid and partly as a viscous liquid, depending on temperature and rate.

1. What Rubber Is

Crystallinity
Ordered packing of chain sections. Requires a regular chain structure.

1. What Rubber Is

Strain crystallization
Crystallization caused by stretching; reversible, and a source of strength in natural rubber.

1. What Rubber Is

Green strength
The strength of uncured compound; determines whether a shaped part holds together before cure.

1. What Rubber Is

Bound styrene
The styrene content of an SBR grade. A primary property variable.

1. What Rubber Is

Volume swell
Increase in volume after immersion in a fluid; primarily a property of the polymer chemistry.

1. What Rubber Is

Constant viscosity (CV) grade
Natural rubber treated to prevent storage hardening.

1. What Rubber Is

Vulcanization
The reaction that crosslinks polymer chains into an elastic network.

1. What Rubber Is

Modulus (rubber usage)
Stress at a stated elongation, such as M100. Not a true modulus; see Module 10.

1. What Rubber Is

Reinforcement
The increase in strength and stiffness that filler gives a compound.

1. What Rubber Is

Accelerator
Chemical controlling how fast a compound cures and how long it can be worked first.

1. What Rubber Is

2. Vulcanization

Crosslink density
Number of crosslinks per unit volume. Controls most cured properties.

2. Vulcanization

Monosulfidic / disulfidic / polysulfidic
Crosslinks containing one, two, or several sulfur atoms.

2. Vulcanization

Conventional cure
High sulfur, low accelerator. Mostly polysulfidic; best tensile and fatigue, poor heat aging.

2. Vulcanization

EV (efficient vulcanization)
Low sulfur, high accelerator. Mostly monosulfidic; best heat aging, poorer fatigue.

2. Vulcanization

Semi-EV
An intermediate cure system balancing aging resistance against fatigue life.

2. Vulcanization

Sulfur donor
A chemical such as TMTD that supplies sulfur without adding elemental sulfur.

2. Vulcanization

Activator
Zinc oxide plus stearic acid, which make the accelerator and sulfur work efficiently together.

2. Vulcanization

Sulfenamide
Accelerator class giving delayed action then fast cure. The standard for high-volume production.

2. Vulcanization

MDR (moving die rheometer)
Instrument that plots torque against time at cure temperature.

2. Vulcanization

ML / MH
Minimum and maximum torque on the cure curve.

2. Vulcanization

ts2
Time to a two-unit torque rise above minimum. Rheometer scorch, the onset of cure.

2. Vulcanization

t90
Time to 90 percent of maximum torque. The practical definition of optimum cure.

2. Vulcanization

Scorch
Premature vulcanization during processing. Defines available working time.

2. Vulcanization

Residual scorch time
The scorch time remaining after heat history already accumulated in earlier steps.

2. Vulcanization

Marching modulus
Continued slow stiffening past the cure plateau.

2. Vulcanization

Reversion
Loss of stiffness on overcure as unstable crosslinks break down.

2. Vulcanization

10 °C rule
Rule of thumb that a 10 °C rise roughly halves cure time.

2. Vulcanization

Coagent
A multifunctional monomer used with peroxides to raise crosslinking efficiency.

2. Vulcanization

State of cure
How far the crosslinking reaction has progressed relative to its achievable maximum.

2. Vulcanization

Induction period
The flat early region of a cure curve where accelerator chemistry proceeds but no crosslinks yet form.

2. Vulcanization

Zinc stearate
The soluble zinc species formed from zinc oxide and stearic acid; the form in which zinc actually activates the cure.

2. Vulcanization

PVI (prevulcanisation inhibitor)
An additive that extends scorch time with little effect on cure rate or final modulus.

2. Vulcanization

Retarder
An additive that delays cure onset, but at the cost of cure rate and modulus.

2. Vulcanization

Bloom
Any ingredient migrating to the surface and becoming visible; wax bloom is intended, sulfur bloom is not.

2. Vulcanization

Work-away stock
Previously processed compound reintroduced into a fresh batch; it carries heat history with it.

2. Vulcanization

Resin cure
Crosslinking with a phenolic resin, giving all-carbon crosslinks with exceptional heat stability.

2. Vulcanization

Compression set
The fraction of a compression not recovered after release; the key seal property.

2. Vulcanization

Dispersion
Breaking agglomerates apart and distributing filler uniformly through the polymer.

2. Vulcanization

3. Elastomer Families

ESBR / SSBR
Emulsion and solution polymerized SBR. Emulsion processes more easily; solution performs better.

3. Elastomer Families

High-cis BR
Polybutadiene above about 90 percent cis-1,4. Best abrasion resistance and resilience.

3. Elastomer Families

Termonomer
The third monomer in a terpolymer, such as the diene in EPDM.

3. Elastomer Families

ENB / DCPD / 1,4-hexadiene
The common EPDM dienes. ENB cures fastest, hexadiene gives best set and scorch safety, DCPD is cheapest.

3. Elastomer Families

Halobutyl
Chlorinated or brominated butyl. Cures faster and co-cures with high-unsaturation rubbers.

3. Elastomer Families

ACN content
The acrylonitrile fraction in NBR. Higher means better oil resistance but worse low temperature.

3. Elastomer Families

HNBR
Hydrogenated nitrile. Most backbone unsaturation removed for heat and ozone resistance.

3. Elastomer Families

Cure compatibility
Whether two blended elastomers cure at similar rates rather than one drawing curatives from the other.

3. Elastomer Families

Microstructure
The proportion of cis, trans, and vinyl repeat units in a diene polymer; set by the catalyst.

3. Elastomer Families

Co-vulcanisation
Two compounds forming networks across their shared interface during cure.

3. Elastomer Families

Building tack
The ability of uncured compound to stick to itself, needed when assembling a part from layers.

3. Elastomer Families

Service group
The working classification into general purpose, solvent resistant, and temperature resistant.

3. Elastomer Families

Layered construction
Using an expensive polymer only as a thin liner where it contacts the aggressive fluid.

3. Elastomer Families

4. Fillers

Aggregate
The fused cluster of carbon black particles; the smallest unit that can be dispersed.

4. Fillers

Agglomerate
A loose cluster of aggregates held by weak attraction; what mixing breaks down.

4. Fillers

Surface area
Filler area per gram. The main driver of reinforcement, encoded in the ASTM grade digit.

4. Fillers

Structure
How branched and irregular filler aggregates are. Drives viscosity, modulus, and green strength.

4. Fillers

Hard / soft black
Hard blacks (N100–N300) are fine and highly reinforcing; soft blacks (N500 and above) are coarser.

4. Fillers

Filler network
Aggregates touching each other at low strain; the main source of hysteresis in a filled compound.

4. Fillers

Bound rubber
Polymer immobilised at the filler surface; a measure of filler-polymer interaction.

4. Fillers

Silanol
The reactive hydroxyl group on a silica surface, responsible for silica's distinctive behaviour.

4. Fillers

Silane coupling agent
A molecule bridging silica to polymer, restoring reinforcement and reducing cure interference.

4. Fillers

5. Plasticizers and Antidegradants

Process oil
Petroleum plasticizer that lowers viscosity by separating chains without reacting with them.

5. Plasticizers and Antidegradants

Paraffinic / naphthenic / aromatic
The three process oil types, from least to most polar; matched to polymer for compatibility.

5. Plasticizers and Antidegradants

Bleeding
Oil migrating out of a compound to the surface, from incompatibility or overloading.

5. Plasticizers and Antidegradants

Extraction
Loss of plasticizer into a contacting fluid; can cause a part to shrink and harden rather than swell.

5. Plasticizers and Antidegradants

Antioxidant
Chemical that interrupts the free-radical chain reaction of oxidation; consumed as it works.

5. Plasticizers and Antidegradants

Antiozonant
Chemical that migrates to the surface and reacts with ozone before it attacks the polymer.

5. Plasticizers and Antidegradants

PPD
Paraphenylenediamine, the most common chemical antiozonant class. Staining.

5. Plasticizers and Antidegradants

Staining
Either the compound darkening itself, or an ingredient migrating out and discolouring what it touches.

5. Plasticizers and Antidegradants

Peptizer
Additive that permanently lowers viscosity by cutting polymer chains during mixing.

5. Plasticizers and Antidegradants

Tackifier
Additive that increases the ability of uncured compound to stick to itself.

5. Plasticizers and Antidegradants

6. Cure System Design

Primary accelerator
The accelerator setting the basic character of the cure, chiefly scorch delay. Usually a sulfenamide.

6. Cure System Design

Secondary accelerator
A faster accelerator added at low level to tune cure rate.

6. Cure System Design

CBS / TBBS / MBS
The common sulfenamide primaries. MBS is secondary-amine derived and subject to nitrosamine concerns.

6. Cure System Design

MBT / MBTS
Thiazole accelerators. MBTS gives safer processing than MBT.

6. Cure System Design

TMTD
A thiuram accelerator that is also a sulfur donor, so it raises modulus as well as cure rate.

6. Cure System Design

DPG
A guanidine secondary accelerator used to boost a sulfenamide.

6. Cure System Design

ETU
Ethylene thiourea, the standard accelerator for polychloroprene metal oxide cures.

6. Cure System Design

Insoluble sulfur
A polymeric sulfur form that resists blooming. It reverts progressively to the soluble form above roughly 105–110 °C, depending on temperature and residence time.

6. Cure System Design

Acid acceptor
A metal oxide that neutralises hydrogen chloride released by halogenated polymers.

6. Cure System Design

Nitrosamine
A carcinogenic compound that can form from secondary-amine derived accelerators; regulated in several regions.

6. Cure System Design

7. Reading and Building a Formulation

Formulation
The complete list of ingredients and quantities that define a compound.

7. Reading and Building a Formulation

Specific gravity
Density relative to water; needed to convert a phr recipe into volume and batch weight.

7. Reading and Building a Formulation

Fill factor
The fraction of mixer chamber volume occupied by the batch, typically 0.70 to 0.75.

7. Reading and Building a Formulation

Batch weight
Chamber volume multiplied by compound specific gravity and fill factor.

7. Reading and Building a Formulation

Cost per volume
Cost per kilogram multiplied by specific gravity; the basis that tracks cost per part.

7. Reading and Building a Formulation

Starting formulation
A published or in-house recipe used as the basis for a new compound.

7. Reading and Building a Formulation

Property specification
A requirement defined by properties rather than by recipe, leaving formulation to the supplier.

7. Reading and Building a Formulation

Change control
The documented process for recording what was changed in a formulation, why, and what was tested.

7. Reading and Building a Formulation

8. Mixing

Internal mixer
An enclosed two-rotor mixer with a hydraulic ram; the main mixing machine in the industry.

8. Mixing

Two-roll mill
An open pair of counter-rotating rolls used for cooling, sheeting, warming, and adding curatives.

8. Mixing

Friction ratio
The speed difference between mill rolls; what generates shear in the nip.

8. Mixing

Incorporation
Drawing ingredients into a single coherent mass wetted by polymer.

8. Mixing

Distribution
Spreading material uniformly through the batch. Distinct from dispersion.

8. Mixing

Ram pressure
Force applied by the ram to keep material in the rotor path.

8. Mixing

Specific energy
Work done per unit mass of compound; the best single criterion for terminating a mix.

8. Mixing

Drop temperature
Batch temperature at discharge; the most closely watched mixing parameter.

8. Mixing

Upside-down mixing
Loading fillers and oils before polymer; faster, but less controlled peak shear.

8. Mixing

Batch-off
Cooling and sheeting a mixed batch before storage.

8. Mixing

Mastication
Deliberate breakdown of polymer molecular weight by shear, mainly for natural rubber.

8. Mixing

9. Test Standards and Batch Release

Test method
A standardised procedure specifying specimen, conditioning, equipment, conditions, and reporting.

9. Test Standards and Batch Release

Repeatability
Agreement between results from the same operator, equipment, and material over a short period.

9. Test Standards and Batch Release

Reproducibility
Agreement between results from different laboratories. Always worse than repeatability.

9. Test Standards and Batch Release

Precision statement
The section of a method quantifying expected scatter within and between laboratories.

9. Test Standards and Batch Release

Conditioning
Holding a specimen at specified temperature and humidity before testing so it reaches equilibrium.

9. Test Standards and Batch Release

Batch release
The decision to allow a mixed compound into production, based on a small set of fast tests.

9. Test Standards and Batch Release

Qualification testing
Slower, less frequent testing establishing that a compound meets the full specification.

9. Test Standards and Batch Release

Fingerprint
The established set of release values characteristic of a compound, used for comparison.

9. Test Standards and Batch Release

Common cause variation
The ordinary noise of a stable process; reacting to it increases variation.

9. Test Standards and Batch Release

Special cause variation
Variation from an identifiable change; appears as a shift, trend, or outlier.

9. Test Standards and Batch Release

Measurement system variation
The share of observed variation contributed by the test rather than the material.

9. Test Standards and Batch Release

10. Physical and Product Testing

Shore A
The standard hardness scale for most rubbers, measuring resistance to indentation.

10. Physical and Product Testing

Ks
Static spring rate — force per unit deflection under steady load. A property of the part, not the compound.

10. Physical and Product Testing

Kd
Dynamic spring rate — the equivalent under cyclic load. Normally higher than Ks in filled compounds, and dependent on frequency, amplitude and temperature.

10. Physical and Product Testing

Kd/Ks
Dynamic-to-static ratio; how much a part stiffens under cyclic loading.

10. Physical and Product Testing

tan δ
Loss factor — the ratio of energy dissipated to energy stored per cycle.

10. Physical and Product Testing

Storage modulus (E′)
The elastic component of the dynamic response; energy stored and returned.

10. Physical and Product Testing

Loss modulus (E″)
The viscous component; energy dissipated as heat.

10. Physical and Product Testing

Payne effect
The fall in dynamic stiffness with increasing strain amplitude, caused by filler network breakdown.

10. Physical and Product Testing

Shape factor
The ratio of loaded area to free area; determines how much a bonded rubber block can bulge.

10. Physical and Product Testing

TR-10
Temperature retraction test estimating the lowest temperature at which a compound behaves elastically.

10. Physical and Product Testing

Brittleness point
The temperature at which a specimen fractures when struck or bent rapidly.

10. Physical and Product Testing

Typical value
The middle of a property distribution; roughly half of production falls below it.

10. Physical and Product Testing

11. Putting It Together

Last known good state
The most recent condition where everything behaved correctly; the right comparison point in an investigation.

11. Putting It Together

Shared compound
A compound used across several parts, which couples those applications together when it changes.

11. Putting It Together

Propagation
The way a change made for one reason produces consequences elsewhere, often in another department.

11. Putting It Together

Blind spot
A failure mode that routine testing does not detect — dispersion is the classic example.

11. Putting It Together