Failure Mode and Effects Analysis (FMEA)

Failure Mode and Effects Analysis:
Failure mode and effects analysis (FMEA; often written with "failure modes" in plural) is the process of reviewing as many components, assemblies, and subsystems as possible to identify potential failure modes in a system and their causes and effects.
For each component, the failure modes and their resulting effects on the rest of the system are recorded in a specific FMEA worksheet. There are numerous variations of such worksheets. A FMEA can be a qualitative analysis, but may be put on a quantitative basis when mathematical failure rate models  are combined with a statistical failure mode ratio database. It was one of the first highly structured, systematic techniques for failure analysis. It was developed by reliability engineers in the late 1950s to study problems that might arise from malfunctions of military systems. An FMEA is often the first step of a system reliability study.
A few different types of FMEA analyses exist, such as:
- Functional
- Design
- Process
Sometimes FMEA is extended to FMECA (failure mode, effects, and criticality analysis) to indicate that criticality analysis is performed too.
FMEA is an inductive reasoning (forward logic) single point of failure analysis and is a core task in reliability engineering, safety engineering and quality engineering.
A successful FMEA activity helps identify potential failure modes based on experience with similar products and processes—or based on common physics of failure logic. It is widely used in development and manufacturing industries in various phases of the product life cycle. Effects analysis refers to studying the consequences of those failures on different system levels.
Functional analyses are needed as an input to determine correct failure modes, at all system levels, both for functional FMEA or Piece-Part (hardware) FMEA. An FMEA is used to structure Mitigation for Risk reduction based on either failure (mode) effect severity reduction or based on lowering the probability of failure or both. The FMEA is in principle a full inductive (forward logic) analysis, however the failure probability can only be estimated or
reduced by understanding the failure mechanism. Hence, FMEA may include information on causes of failure (deductive analysis) to reduce the possibility of occurrence by eliminating identified (root) causes.

Introduction:
The FME(C)A is a design tool used to systematically analyze postulated component failures and identify the resultant effects on system operations. The analysis is sometimes characterized as consisting of two sub-analyses, the first being the failure modes and effects analysis (FMEA), and the second, the criticality analysis (CA).
Successful development of an FMEA requires that the analyst include all significant failure modes for each contributing element or part in the system. FMEAs can be performed at the system, subsystem, assembly, subassembly or part level. The FMECA should be a living document during development of a hardware design. It should be scheduled and completed concurrently with the design. If completed in a timely manner, the FMECA can help guide design decisions. The usefulness of the FMECA as a design tool and in the decision making process is dependent on the effectiveness and timeliness with which design problems are identified. Timeliness is probably the most important consideration. In the extreme case, the FMECA would be of little value to the design decision process if the analysis is performed after the hardware is built. While the FMECA identifies all part failure modes, its primary benefit is the early identification of all critical and catastrophic subsystem or system failure modes so they can be eliminated or minimized through design modification at the earliest point in the development effort; therefore, the FMECA should be performed at the system level as soon as preliminary design information is available and extended to the lower levels as the detail design progresses.

Remark: For more complete scenario modelling another type of Reliability analysis may be considered, for example fault tree analysis (FTA); a deductive (backward logic) failure analysis that may handle multiple failures within the item and/or external to the item including maintenance and logistics. It starts at higher functional / system level. A FTA may use the basic failure mode FMEA records or an effect summary as one of its inputs (the basic events). Interface hazard analysis, human error analysis and others may be added for completion in scenario modelling.
Functional Failure mode and effects analysis The analysis may be performed at the functional level until the design has matured sufficiently to identify specific hardware that
will perform the functions; then the analysis should be extended to the hardware level. When performing the hardware level FMECA, interfacing hardware is considered to be operating within specification. In addition, each part failure postulated is considered to be the only failure in the system (i.e., it is a single failure analysis). In addition to the FMEAs done on systems to evaluate the impact lower level failures have on system operation, several other FMEAs are done. Special attention is paid to interfaces between systems and in fact at all functional interfaces. The purpose of these FMEAs is to assure that irreversible physical and/or functional damage is not propagated across the interface as a result of failures in one of the interfacing units. These analyses are done to the piece part level for the circuits that directly interface with the other units. The FMEA can be accomplished without a CA, but a CA requires that the FMEA
has previously identified system level critical failures. When both steps are done, the total process is called a FMECA.

Types:
Functional: before design solutions are provided (or only on high level) functions can be evaluated on potential functional failure effects. General Mitigations ("design to" requirements) can be proposed to limit consequence of functional failures or limit the probability of occurrence in this early development. It is based on a functional breakdown of a system. This type may also be used for Software evaluation.
Concept Design / Hardware: analysis of systems or subsystems in the early design concept stages to analyse the failure mechanisms and lower level functional failures, specially to different concept solutions in more detail. It may be used in trade-off studies.
Detailed Design / Hardware: analysis of products prior to production. These are the most detailed (in mil 1629 called Piece-Part or Hardware FMEA) FMEAs and used to identify any possible hardware (or other) failure mode up to the lowest part level. It should be based on hardware breakdown (e.g. the BoM = Bill of Material). Any Failure effect Severity, failure Prevention (Mitigation), Failure Detection and Diagnostics may be fully analyzed in this FMEA.
Process: analysis of manufacturing and assembly processes. Both quality and reliability may be affected from process faults. The input for this FMEA is amongst others a work process / task Breakdown.

Ground rules
The ground rules of each FMEA include a set of project selected procedures; the assumptions on which the analysis is based; the hardware that has been included and excluded from the analysis and the rationale for the exclusions. The ground rules also describe the indenture level of the analysis (i.e. the level in the hierarchy of the part to the sub-system, sub-system to the system, etc.), the basic hardware status, and the criteria for system and mission success. Every effort should be made to define all ground rules before the FMEA begins; however, the ground rules may be expanded and clarified as the analysis proceeds. A typical set of ground rules (assumptions) follows:
1. Only one failure mode exists at a time.
2. All inputs (including software commands) to the item being analyzed are present and at nominal values.
3. All consumables are present in sufficient quantities.
4. Nominal power is available Benefits
Major benefits derived from a properly implemented FMECA effort are as follows:
1. It provides a documented method for selecting a design with a high probability of successful operation and safety.
2. A documented uniform method of assessing potential failure mechanisms, failure modes and their impact on system operation, resulting in a list of failure modes ranked according to the seriousness of their system impact and likelihood of occurrence.
3. Early identification of single failure points (SFPS) and system interface problems, which may be critical to mission success and/or safety. They also provide a method of verifying that switching between redundant elements is not jeopardized by postulated single failures.
4. An effective method for evaluating the effect of proposed changes to the design and/or operational procedures on mission success and safety A basis for in-flight troubleshooting procedures and for locating performance monitoring and fault-detection devices.
6. Criteria for early planning of tests. 

From the above list, early identifications of SFPS, input to the troubleshooting procedure and locating of performance monitoring / fault detection devices are probably the most important benefits of the FMECA. In addition, the FMECA procedures are straightforward and allow orderly evaluation of the design.

Basic terms:
The following covers some basic FMEA terminology.
Failure
The loss of a function under stated conditions.
Failure mode
The specific manner or way by which a failure occurs in terms of failure of the item (being a part or (sub) system) function under investigation; it may generally describe the way the failure occurs. It shall at least clearly describe a (end) failure state of the item (or function in case of a Functional FMEA) under consideration. It is the result of the failure mechanism (cause of the failure mode). For example; a fully fractured axle, a deformed axle or a fully open or fully closed electrical contact are each a separate failure mode of a DFMEA, they would not be failure modes of a PFMEA. Here you examine your process, so process step x - insert drill bit, the failure mode would be insert wrong drill bit, the effect of this is too big a hole or too small a hole.

Failure cause and/or mechanism
Defects in requirements, design, process, quality control, handling or part application, which are the underlying cause or sequence of causes that initiate a process (mechanism) that leads to a failure mode over a certain time. A failure mode may have more causes. For example; "fatigue or corrosion of a structural beam" or "fretting corrosion in an electrical contact" is a failure mechanism and in itself (likely) not a failure mode. The related failure mode (end state) is a "full fracture of structural beam" or "an open electrical contact". The initial cause might have been "Improper application of corrosion protection layer (paint)" and /or "(abnormal) vibration input from another (possibly failed) system".

Failure effect
Immediate consequences of a failure on operation, function or functionality, or status of some item.
Indenture levels (bill of material or functional breakdown)
An identifier for system level and thereby item complexity. Complexity increases as levels are closer to one.
Local effect
The failure effect as it applies to the item under analysis.
Next higher level effect
The failure effect as it applies at the next higher indenture level.
End effect
The failure effect at the highest indenture level or total system.
Detection
The means of detection of the failure mode by maintainer, operator or built in detection system, including estimated dormancy period (if applicable)
Probability
The likelihood of the failure occurring.
Risk Priority Number (RPN) Severity (of the event) × Probability (of the event occurring) × Detection (Probability that the event would not be detected before the user was aware of it)
Severity
The consequences of a failure mode. Severity considers the worst potential consequence of a failure, determined by the degree of injury, property damage, system damage and/or time lost to repair the failure.
Remarks / mitigation / actions
Additional info, including the proposed mitigation or actions used to lower a risk or justify a risk level or scenario.

Probability (P)
It is necessary to look at the cause of a failure mode and the likelihood of occurrence. This can be done by analysis, calculations / FEM, looking at similar items or processes and the
failure modes that have been documented for them in the past. A failure cause is looked upon as a design weakness. All the potential causes for a failure mode should be identified and documented. This should be in technical terms. Examples of causes are: Human errors in handling, Manufacturing induced faults, Fatigue, Creep, Abrasive wear, erroneous algorithms, excessive voltage or improper operating conditions or use (depending on the used ground rules). A failure mode is given a
Probability Ranking.
Severity (S)
Determine the Severity for the worst-case scenario adverse end effect (state). It is convenient to write these effects down in terms of what the user might see or experience in terms of functional failures. Examples of these end effects are: full loss of function x,
degraded performance, functions in reversed mode, too late functioning, erratic functioning, etc. Each end effect is given a Severity number (S) from, say, I (no effect) to V (catastrophic),
based on cost and/or loss of life or quality of life. These numbers prioritize the failure modes (together with probability and detectability). Below a typical classification is given. Other
classifications are possible. See also hazard analysis.
Detection (D)
The means or method by which a failure is detected, isolated by operator and/or maintainer and the time it may take. This is
important for maintainability control (availability of the system) and it is especially important for multiple failure scenarios. This
may involve dormant failure modes (e.g. No direct system effect, while a redundant system / item automatically takes over or when the failure only is problematic during specific mission or system states) or latent failures (e.g. deterioration failure mechanisms, like a metal growing crack, but not a critical length). It should be made clear how the failure mode or cause can be discovered by an operator under normal system operation or if it can be
discovered by the maintenance crew by some diagnostic action or automatic built in system test. A dormancy and/or latency period may be entered.
Dormancy or Latency Period
The average time that a failure mode may be undetected may be entered if known. For example:
- Seconds, auto detected by maintenance computer
- 8 hours, detected by turn-around inspection
- 2 months, detected by scheduled maintenance block X
- 2 years, detected by overhaul task x

Indication
If the undetected failure allows the system to remain in a safe / working state, a second failure situation should be explored to determine whether or not an indication will be evident to all operators and what corrective action they may or should take.
Indications to the operator should be described as follows:
- Normal. An indication that is evident to an operator when the system or equipment is operating normally.
- Abnormal. An indication that is evident to an operator when the system has malfunctioned or failed.
- Incorrect. An erroneous indication to an operator due to the malfunction or failure of an indicator (i.e., instruments, sensing devices, visual or audible warning devices, etc.).

Risk level (P×S) and (D)
Risk is the combination of End Effect Probability And Severity where probability and severity includes the effect on non detectability (dormancy time). This may influence the end effect probability of failure or the worst case effect Severity. The exact calculation may not be easy in all cases, such as those where multiple scenarios (with multiple events) are possible and detectability / dormancy plays a crucial role (as for redundant systems). In that case Fault Tree Analysis and/or Event Trees may be needed to determine exact probability and risk levels.
Preliminary Risk levels can be selected based on a Risk Matrix like shown below, based on Mil. Std. 882. The higher the Risk level, the more justification and mitigation is needed to provide evidence and lower the risk to an acceptable level. High risk should be indicated to higher level management, who are responsible for final decision-making.

Timing:
The FMEA should be updated whenever:
- A new cycle begins (new product/process)
- Changes are made to the operating conditions
- A change is made in the design
- New regulations are instituted
- Customer feedback indicates a problem

Uses:
- Development of system requirements that minimize the likelihood of failures.
- Development of designs and test systems to ensure that the failures have been eliminated or the risk is reduced to acceptable level.
- Development and evaluation of diagnostic systems
- To help with design choices (trade-off analysis).

Advantages:
- Catalyst for teamwork and idea exchange between functions
- Collect information to reduce future failures, capture engineering knowledge
- Early identification and elimination of potential failure modes
- Emphasize problem prevention
- Improve company image and competitiveness
- Improve production yield
- Improve the quality, reliability, and safety of a product/process
- Increase user satisfaction
- Maximize profit
- Minimize late changes and associated cost
- Reduce impact on company profit margin
- Reduce system development time and cost
- Reduce the possibility of same kind of failure in future
- Reduce the potential for warranty concerns.

Advanced product quality planning

Advanced product quality planning:
Advanced product quality planning (APQP) is a framework of procedures and techniques used to develop products in industry, particularly in the automotive industry. It is similar to the concept of Design for Six Sigma (DFSS).
According to the Automotive Industry Action Group (AIAG), the purpose of APQP is "to produce a product quality plan which will support development of a product or service that will satisfy the customer." It is the process employed by General Motors, Ford, Chrysler and their suppliers for their product development systems.

Advanced product quality planning is a process developed in the late 1980s by a commission of experts who gathered around the 'Big Three' of the US automobile industry: Ford, GM and Chrysler.
Representatives from the three automotive original equipment manufacturers (OEMs) and the Automotive Division of American Society for Quality Control (ASQC)* created the Supplier Quality Requirement Task Force for developing a common understanding on topics of mutual interest within the automotive industry.
This commission invested five years to analyze the then-current automotive development and production status in the US, Europe and especially in Japan. At the time, the success of the Japanese automotive companies was starting to be remarkable in the US market.
APQP is utilized today by these three companies and some affiliates. Tier 1 suppliers are typically required to follow APQP procedures and techniques and are also typically required to be audited and registered to IATF 16949. This methodology is now being used in other manufacturing sectors as well.
The basis for the make-up of a process control plan is included in the APQP manual. The APQP process is defined in the AIAG's APQP manual, which is part of a series of interrelated documents that the AIAG controls and publishes.

These manuals include:
- The failure mode and effects analysis (FMEA) manual
- The statistical process control (SPC) manual
- The measurement systems analysis (MSA) manual
- The production part approval process (PPAP) manual
The Automotive Industry Action Group (AIAG) is a non-profit association of automotive companies founded in 1982.
APQP serves as a guide in the development process and also a standard way to share results between suppliers and automotive companies.

APQP specifies three phases:
Development, Industrialization and Product Launch. Through these phases 23 main topics will be monitored. These 23 topics will be all completed before the production is started. 
They cover such aspects as: design robustness, design testing and specification compliance, production process design, quality inspection standards, process capability, production capacity, product packaging, product testing and operator training plan, among other items.

APQP focuses on:
- Up-front quality planning.
- Determining if customers are satisfied by evaluating the output and supporting continual improvement.

APQP consists of five phases:
- Plan and Define Program
- Product Design and Development Verification
- Process Design and Development Verification
- Product and Process Validation and Production Feedback
- Launch, Assessment & Corrective Action.

The APQP process has seven major elements:
- Understanding the needs of the customer
- Proactive feedback and corrective action
- Designing within the process capabilities
- Analyzing and mitigating failure modes
- Verification and validation
- Design reviews
- Control special/critical characteristics.

Advanced Product Quality Planning (APQP) Checklist

Advanced Product Quality Planning (APQP) Checklist:

Advanced Product Quality Planning (APQP) is a quality framework used for developing new products in the automotive industry. It can be applied to any industry and is similar in many respects to the concept of design for six sigma (DFSS). The APQP process is described in AIAG manual 810-358-3003. Its purpose is “to produce a product quality plan which will support development of a product or service that will satisfy the customer.” It does this by focusing on:

  • Up-front quality planning
  • Evaluating the output to determine if customers are satisfied & support continual improvement

The Advanced Product Quality Planning process consists of four phases and five major activities along with ongoing feedback assessment and corrective action as shown below.

A further indication of the APQP process is to examine the process outputs by phase. This is shown in the table below:The APQP process involves these major elements:
  • Understand customer needs . This is done using voice of the customer techniques to determine customer needs and using quality function deployment to organize those needs and translate them into product characteristics/requirements.
  • Proactive feedback & corrective action. The advance quality planning process provides feedback from other similar projects with the objective of developing counter-measures on the current project. Other mechanisms with verification and validation, design reviews, analysis of customer feedback and warranty data also satisfy this objective.
  • Design within process capabilities. This objective assumes that the company has brought processes under statistical control, has determined its process capability and has communicated it process capability to its development personnel. Once this is done, development personnel need to formally determine that critical or special characteristics are within the enterprise’s process capability or initiate action to improve the process or acquire more capable equipment.
  • Analyze & mitigate failure modes. This is done using techniques such as failure mode and effects analysis or anticipatory failure determination.
  • Verification & validation. Design verification is testing to assure that the design outputs meet design input requirements. Design verification may include activities such as: design reviews, performing alternate calculations, understanding tests and demonstrations, and review of design documents before release. Validation is the process of ensuring that the product conforms to defined user needs, requirements, and/or specifications under defined operating conditions. Design validation is performed on the final product design with parts that meet design intent. Production validation is performed on the final product design with parts that meet design intent produced production processes intended for normal production.
  • Design reviews . Design reviews are formal reviews conducted during the development of a product to assure that the requirements, concept, product or process satisfies the requirements of that stage of development, the issues are understood, the risks are being managed, and there is a good business case for development. Typical design reviews include: requirements review, concept/preliminary design review, final design review, and a production readiness/launch review.
  • Control special/critical characteristics. Special/critical characteristics are identified through quality function deployment or other similar structured method. Once these characteristics are understood, and there is an assessment that the process is capable of meeting these characteristics (and their tolerances), the process must be controlled. A control plan is prepared to indicate how this will be achieved. Control Plans provide a written description of systems used in minimizing product and process variation including equipment, equipment set-up, processing, tooling, fixtures, material, preventative maintenance and methods.

Polystyrene

Polystyrene:
Polystyrene was first produced commercially by Dow chemical company in 1937.
Polystyrene was first initially used for its excellent dielectric and optical properties.

Monomer Preparation:
Styrene is produced from the ethyl-benzene by a process of dehydrogenation at 630°C.
- Styrene at room temperature is a liquid with boiling  point at 145.2°C.
- Like many aromatic compounds, it has pleasant smell in pure form but looses the same due to traces of ketones and aldehydes if allowed to oxidize by exposure to air.
- It is a solvent for polystyrene and many synthetic rubbers, including SBR, but has only a very limited mutual solubility in water.
- It has a strong tendency to polymerize on heating or on exposure to UV light.

Polymerization 
Polymerization methods
-  Mass 
-  Suspension
-  Solution

Mass Polymerization (Tower Process)
- Styrene is pre-polymerized by heating (without initiators) at 80°C for two days in pre-polymerization kettle.
- Monomer-polymer mixture is then run into a tower which is fitted with heating and cooling jackets and the top of the  tower is maintained at temperature of 110°C, the temperature of about 150°C in between and bottom temperature at 180°C. 
- High temperature  at bottom ensures a high conversion.- Base of the tower forms the hopper of an extruder from which melt emerges as filament which are cooled, disintegrated and packed.

Solution Polymerization 
- Styrene and solvent are blended together and pumped through number of reactors with different heating zones.  
- From the last reactor the polymer is run into devolitilising vessel.
- At a temperature of 225°C, the solvent and the polymer are removed, condensed and polymer is fed into extruder units, extruded as filaments, granulated, and stored.
- Polymerization in solution reduces the exotherm but may lead to problem of solvent recovery and solvent hazards. 

Suspension Polymerization 
- In this process the monomer is suspended in droplets. 
- The reaction is initiated by monomer soluble initiators such as Benzoyl peroxide.
- It is necessary to coat the droplets effectively with some suspension agents e.g. Poly (vinyl alcohol),talc to prevent  them cohering.
- The resulting particle size depends on the quantity of suspension agent and speed of agitation. 
- Following polymerization, unreacted monomer may be removed by steam distillation and the polymer is washed and dried. 

Structure Property Relationship
- PS is linear hydrocarbon polymer.
- Due to steric hindrance of benzene ring causing stiffening effect, the Tg. of commercial polymer is 90° to 110°C. Consequence of this Tg value and amorphous nature of material make it hard and transparent at room temperature.
- It is soluble in benzene, styrene, toluene. The presence of benzene ring in polystyrene having greater reactivity than Polyethylene.
- Due to phenyl group Polystyrene is having limited chemical resistance.

General properties of PS
General properties of Polystyrene are,
-  Hard, rigid and transparent thermoplastic.
-  Low cost, good mouldability.
-  Low water absorption, good dimensional stability.
-  Good electrical insulation properties, colourability.
-  Incorporation of 1% of saturated aliphatic amines, cyclic amines or aminoalcohols has been found to improve greatly the resistance to weathering.
-  It is  brittle in nature.
-  It is enable to withstand the temperature of boiling water.
-  It is having mediocre oil resistance. 

Properties of Polystyrene
Processing Considerations
- Unmodified grades have negligible water absorption.
-  Specific heat of PS is less, therefore higher plasticizing capacity machines should be used.
-  Melts have good stability at processing temperatures.
-  Generally no need to purge while shutting down.
-  Recycling percentage should not be more than 15-20% in injection moulding.
-  Due to amorphous innature, polymer gives low mould shrinkage.
-  Polystyrene melts are of medium viscosity but highly pseudo plastic.  

Processing Techniques
- Injection Moulding 
- Plastic temperature in the process range from 200° C to 250°C for GPPS and 180° to 250°C for HIPS grades.
-  Injection pressures are of 30 to 275 MPa  depends on the grade of the material.  
- Typical mould temperature is 10-80°C.

Extrusion 
Typical extrusion conditions 
- Temperature profile  150-200°C
- Recommended screw L/D ratio 25:1 to 30:1
- Recommended compression ratio 2:1 to 3:1

Grading of Polystyrene
General purpose polystyrene (GPPS)
- Good balance is maintained to have good heat resistance, reasonably high setting-up temperature, good flow properties and moderate impact strength.
High molecular weight polystyrene (HMPS)
- HMPS gives impact strength without the loss of clarity.
Heat resistant grade
- By reducing monomer content from 5% to 0%, softening point may raised from 70°C to 100°C.
Easy flow grade
- It can be obtained by using low molecular material, by using internal lubricant , by using external lubricant and by controlling size and shape of granules.

Expanded Polystyrene
- Bead (Suspension )Polymerization  is generally used for manufacturing expanded polystyrene.
- Blowing agents may be incorporated before polymerization or used to impregnate the bead under heat and pressure in a post-polymerization operation.
- The impregnated beads may then be processed by two basically different techniques.
Steam moulding process.
- Direct injection moulding or extrusion.
- The beads can be expanded to about 40 times their previous size with densities as low as 16 kg / cm3.

Applications of PS
Household
- Items like power boxes, combs, toys, bangles, decorative gift articles, ball pen, water jug, mugs, plates, trays, racks, boxes, jar, etc.

Automobile 
- In automobile industries automatic parts like reflector, doom lights, display signs and automotive penal covers.

Electrical/Electronics
- Many electrical and electronic items like light diffusers battery cases, electrical coil forms,TV and transistor cabinets, refrigerator, door and body liners, floppy storage boxes.

Medical 
-  Medical applications like disposable syringe.

Packaging 
-  Thin walled packaging, containers, disposable transparent containers, bottles, utility boxes, packaging of fish, bottle caps.

Industrial 
-   Battery cases, filling cabinets, quick dry emulsion paints, blade dispenser, foot rules and lay flat produce boxes.

Building 
-  Bathroom accessories like toilet seats, Flooring & ceiling channels and profiles, wall tiles, towel racks, window envelop and building 

Additives of Polyurethane

Additives of Polyurethane:
Functional Additives: Additives for controlling reaction rate, protecting against ageing, increasing flame resistance, for foaming, colouring, filling, reinforcing, etc. 
Catalysts : Catalysts include tertiary amines, salts of weak acids, organometallics, phosphorus compounds, etc. 
Inhibitors: Less well known are inhibitors of the isocyanate reaction which include hydrochloric acid, benzoyl chloride and p-toluene sulfonic acid. 
Cross-linking agents and chain extenders: Used in cold curing, rigid and integral foams. OH- and NH-functional cross-linking agents and chain extenders are of major importance particularly diols and amines. 
Surfactants: It ensure that the water polyisocyanate reaction leads to a uniform blowing reaction during the manufacture of PU foams.

Foam Stabilizer: The main foam stabilizers are water-soluble polyether siloxanes. 
Cell regulators:  Act mainly as defoaming agents. The most important are based on methyl polysiloxanes. 
Blowing agents: They are required to foam polyurethanes. Several methods can be used 
- CO2 is generated by reacting isocyanate with water; this serves as a chemically generated blowing gas; 
- Low boiling liquids (e.g. the chlorinated fluoroalkanes and methylene chloride) are vaporised and physically foam the exothermic reaction mixture;
- A foam is mechanically produced by blowing or whipping-in air. 
- The first method is preferred for flexible foams, the second for rigid foams and the third for foam coatings. 

Flame retardants:  Halogen and phosphorus compounds,  Aluminium hydroxide  control flammability and flame spread 
Anti-ageing agents, Sterically hindered phenols and secondary aromatic amines are used.
UV Stabilizers: Light resistant polyurethanes can be manufactured using aliphatic isocyanates.
Bis-benzo-oxazoles, cumarene derivatives and bis(steryl)bisphenyls are used as UV stabilizers 
Pigments and colourant: Inorganic pigments titanium dioxide, iron oxides, chromium oxides, cadmium sulfide, carbon black .etc., 
Organic pigments originate from the range of azo and diazo compounds and phthalocyanines 
Antistatic Agents: The addition of antistatics tetraalkylammoniumalkyl sulfate to the polyol component reduce the surface resistance to  10(8) ohm.

FILLERS
- Fillers used are carbonates (chalk) and these represent about 50% of the total requirement in polyurethanes. 
- Organic extenders used to lower costs include wood, straw, shells and plant materials 
Reinforcements
- Glass fiber is becoming increasingly important because of "high modulus" RIM products.
- Glass (hollow) spheres of 5 to 300 m m diameter improve the properties of rigid foams 

POLYURETHANE CASTING RESINS
- Liquid di-isocyanates (reactive resins) cure after mixing with polyols (curing agent) into moulded PU with various physical properties. 
- Ready to use casting compound also contains fillers, plasticizers and colourants 

STRUCTURE AND PROPERTIES
- The reactive resin reacts with the curing agent as follows.
- Mixing ratios are calculated according to this equation 
- Further components are added to the cross-linkable PU casting compound to obtain specific processing characteristic and properties in the moulded material.
The characteristic properties of cast resins are
-  Can be processed down to 0 ° C, 
-  Low exotherm during curing, 
-  Same casting resin formulation for small and large mouldings, 
-  Rapid curing with catalysts, 
-  Low shrinkage, 
-  Low shrinkage effect on inserts, 
-  Good adhesion on all materials, 
-  High resistance to chemicals, 
-  Low water absorption and permeability to water vapor, 
-  Safe handling, 
-  Low material costs. 

PHYSICAL PROPERTIES
- Specific properties vary widely with composition, but urethane castable elastomers generally have excellent tear, abrasion, impact and wear resistance.

CHEMICAL PROPERTIES
Resistance to Chemicals 
- PU casting resins are resistant to weak acids, alkaline solutions, greases, oils, aliphatic hydrocarbons. They are not resistant to strong acids and alkaline solutions, aromatics, alcohols and hot water. 
Resistance to High Energy Radiation 
- At a dosage of 1012 J kg-I/108 Mrad, tensile strength and elongation at break fall by about 20 %. 
Weathering Resistance
- PU casting resins are weather resistant 

Flammability 
- Chlorine-containing curing agents and additives such as aluminum trihydrate (ATH) act as flame retardants. 
Toxicological Assessment 
- Vapors of all isocyanates are extreme irritants for eyes 
- Greatest damage is caused by inhaling vapors and dust impurities
- MAC (maximum allowed concentration) in the work place has been reduced from 0.1 ppm to 0.02 ppm. 
Polyester polyol :  are non-toxic. 
Cured Resin: Cured PU is non-toxic 

PROCESSING 
Casting 
- Polyol, dehydrating components and other additives are stirred at temperatures of 100 to 120°C under a vacuum of 1 to 10 mbar until no more bubbles rise. 
- Isocyanate components contain no additives and are used as supplied.
- Mixture is stirred for three minutes and cooled to ambient temperature. 
- Insufficient isocyanate leads to soft moulded material, excess to greater hardness 
- Curing time at room temperature is 8 to 10 hours, full cure a further 8 days. Increasing the temperature to 40 and 80O C typically reduces curing time to 90 and 10 minutes, respectively.

PU STRUCTURAL FOAMS 
- Structural foams are manufactured mainly from polyether polyols with butandiol, ethylene glycol, aminopolyols or diamines as cross-linkers. Tertiary amines and organotin compounds are used as catalysts.
- The formation of PU foam in the mould can be controlled so that moulded articles with a cellular core and almost non-cellular surrounding region can be produced 
- The outer zone reaches the density of the basic polymer. Moving towards the middle the density decreases gradually and reaches a minimum in the centre.RIM quasi - pre polymer process
SECONDARY PROCESSING
Joining: PU structural foams are joined using reactive adhesives based on PU, EP and UP  resins. PU structural foams to be screwed together.

AVAILABILITY 
- There is a large variety of solid encapsulating resins and elastomer casting resins.
- Casting resin components are supplied in liquid form. The isocyanate resin is always unmixed.
- Polyol and isocyanate stocks must be protected from moisture. 

APPLICATIONS  
Cast PU Resins
- Casting of cable fittings , bonding and sealing of battery cases, encapsulation of transformers, ignition coils, encased capacitors tops, foundry binders, wear-resistant floor coatings.

Flexible PU Structural Foams 
- Soft-elastic PU integral foams of low density (200 to 300 kg m-3 ) for bicycle saddles or safety components in the interior of cars, e.g. head rests and steering wheel covers; also for moped saddles and motorbike seats. 
- Flexible PU structural foams of moderate density (400 to 600 kg m-3) for shoe soles.
- Tough and resilient PU structural foams of high density (700 to 1000 kg m-3), the so-called micro-cellular elastomers, used for (e.g.) car bodywork such as fenders, external mirrors.
- Solid RIM polyurethane (density around 1100 kg m-3) for external car.
Rigid PU Structural Foams 
- Window and dome light frames, loudspeaker, radio and tape recorder casing, tennis-racket composites, cable sockets, consoles and housings for telex machines, copy and computer-equipment, typewriter casing, seating, beds, tables, laboratory furniture and shop installations.

Polyurethane

Polyurethane:
- Produced by the reaction of a polyfunctional isocyanate with a polyol or other reactant containing two or more groups reactive with isocyanate, most often hydroxyls.
- Hydroxyl-containing component covers a wide range of molecular weights and types, including polyester and polyether polyols. 
- Polyfunctional isocyanates can be aromatic, aliphatic, cycloaliphatic, or polycyclic in structure.
- Flexibility in the selection of reactants leads to the wide range of physical properties that allows polyurethanes to play an important role in the world market.

HISTORICAL DEVELOPMENT
- Discovered by Otto Bayer and co-workers in 1937.
- Vigorous research programme in the laboratories of I. G. Farben- industrie and its successor, Bayer AG, which led to the production of rigid foams, adhesives, and coatings.  
- The recent growth in the commercial importance of polyurethane products formed by reaction injection moulding (RIM). 
- RIM technology permits the conversion of polyurethane elastomers into automotive components, non- automotive products, including business-machine housings and parts for heavy-duty industrial equipment.

Isocyanates 
- Most important isocyanate used in the manufacture of polyurethane is 2,4-tolylene di-isocyanate (TDI) with 2,6 tolylene di-isocyanate and their derivatives.
- If toluene is dinitrated without separation a mixture of about 80% 2,4­dinitrotoluerle and 20% 2,6-dinitrotoluene is obtained. Nitration of   separated 2-nitrotoluene will yield a mixture of approximately 65% of the 2,4- and 35% of the 2,6-isomer 
- Next stage is the reduction of the nitro compounds to amines. Resultant amines are then reacted with phosgene.- Carbamoyl chloride formed may then be decomposed to produce di­isocyanate.- Isocyanates are toxic materials, highly reactive liquids and  care should be exercised in their use. 

Typical Di-isocyanate used in the manufacture of Polyurethane
MANUFACTURE OF POLYURETHANES      
POLYESTER POLYOLS
- Polyesters have several esters groups in their molecule.
- The main methods of manufacture are 
- Esterification of polycarboxylic acids with polyhydroxyl compounds, 
- Transesterification of polycarboxylic acid esters with polyhydroxyl compounds, 
- Polycondensation of hydroxycarboxylic acids, 
- Polymerization of lactones 
- If the diol is partially replaced by a triol such as triethylene glycol, a branched polyester results, the higher the triol content, the greater the degree of branching.
- The polyesters used for manufacturing polyurethanes have mean molecular weights of 2000 and hydroxyl values of 50 to 70.

Polyester polyols for Polyurethane
POLYETHER POLYOLS
- Polyethers are polymerization product of epoxides. 
- They are synthesized from propylene oxide or mixture of ethylene and propylene oxides.
- If a product with three or more active H-atoms instead of two is used, branched polyethers analogous to polyesters result 
- Polyethers used in PU chemistry have molecular weights of 300 to 6000 and functionalities of 2 to 8. 

Polyether Polyols for Polyurethane

Polyvinylidenefluoride (PVDF)

Polyvinylidenefluoride (PVDF):
General Description
- Introduced by Pennwalt Corp. in 1961, PVF2 or PVDF is a high molecular weight homopolymer. 
- The monomer an be obtained from trichloroethylene by reacting with hydrofluoric acid and the action of metallic zinc on the difluorodichloroethane formed.
- The partially crystalline polymer contains over 57% w/w fluorine.
Particular advantages of PVDF are:
- high mechanical strength, stiffness and toughness, 
- relatively resistant to high and low temperatures
- tough even at low temperatures,
- good chemical resistance.
Structure and Properties
- The degree of crystallinity depends on the history of the molding.
- Rapid cooling of thin­ walled moldings and film results in transparent products; slow cooling or annealing at 135°C lead to highly crystalline products with high stiffness and compressive creep strength.
Availability
PVDF is supplied in various grades as:
- granules for injection molding and extrusion,
- as powder and 
- as 45 to 50% dispersions in organic solvents  (dimethyl phthalate & diisobutylketone). 

Mechanical Properties
- Transition Temperatures - PVDF has a glass transition temperature Tg of 40 °C, a crystallization temperature of 140 °C and a melting point of 171 °C.

Thermal Properties
PVDF can be used over the range -60 to +150°C. 
It withstands temperatures as follows without any noticeable degradation:
- 150°C over 1 year,
- 260°C up to 12 hours,
- 240 °C up to 30 minutes,
- at 480 °C it decomposes within a few minutes.
Copper, aluminium and iron catalyze decomposition.

Electrical Properties
-Like PVF, PVC and PVDC, the polar nature of PVDF precludes its use for high frequency applications. 
- The volume resistivity is greater than 1015 Ω at 30 °C making it highly suitable for use in the mains frequency range. 
- The dielectric strength (1 mm film) is 22 kV/mm, the surface resistance exceeds 1013 Ω.
Resistance to Chemicals
- PVDF is resistant to acids (apart from fuming nitric acid), alkaline solutions, solvents, aromatic, aliphatic or chlorinated hydrocarbons, oils, fats, fluoro-refrigerants. 
- It is not resistant to primary amines at elevated temperatures, hot acetone (thin films), strongly polar organic compounds such as dimethylformamide, diethyl acetamide, cyclohexanone, ketones, esters.

Weathering Resistance
- PVDF deteriorates slightly outdoors.

Resistance to Radiation 
- PVDF is resistant to UV; there is slight degradation in the range 200 to 400 nm. 
- Its resistance to high energy radiation is superior to that of other fluoroplastics.
Flammability
- PVDF is classified as V-0 to UL94. The oxygen index is 44%.

Toxicological Assessment
- There are no restrictions on the use of PVDF with foodstuffs. 
- It is non-toxic. 
- Gases liberated during processes must be
ventilated.

Processing - 1
- Injection molding, extrusion and coating are the most important methods of processing PVDF. 
- The storing temperature of coatings produced by spraying, dipping or casting is 190 to 215°C.

Processing-2
- It is absolutely essential that the surfaces of plasticizing screws in injection molders or extruders do not contain any boron. 
- Boron-containing products such as various glass fiber materials or MoS2 are incompatible with PVDF and cause spontaneous decomposition of the product during processing (fire, vaporization). 
- This can also occur with colorants, fillers and reinforcements not certified by the manufacturer. Suitable pigment concentrates are available.

Joining -1 
Welding 
- Welding with round nozzle 345 + 10°C
- Welding with high speed nozzle 350 + 10°C
- Heated tool welding 230 °C
- Melt pressure 0.5 bar
- Welding pressure 2 bar
HF welding is suitable for wall thicknesses up to 2 mm.
Ultrasonic welding: near and remote field methods.

Joining-2
Bonding
- PVDF with PVDF: solvent adhesives as for PVC-U
- PVDF with PVDF or other materials: two-pack adhesives based on Epoxide resin.
 - Surfaces to be bonded must be roughened.

Typical Applications
- Seals, pump and valve components, membranes, transparent rigid pipes (for HF and HC!), fittings, linings for pipes, vessels and autoclaves. films for packaging pharmaceuticals, medical instruments, shrink tubing, corrosion- and weather-resistant laminates for wood and metal, cable sheathing, monofilaments for manufacturing filter cloth and piezo and pyroelectrical films for hydrophones, infrared detectors, respiration monitors, muscle sensors and security equipment.
- Modification of the relatively stiff homopolymer has resulted in more flexible grades thus opening up new applications. The melting range of the modified material is 162 to l65°C.

Typical Applications-1
- Seals, pump and valve components, membranes, transparent rigid pipes (for HF and HC!), fittings, linings for pipes, vessels and autoclaves. films for packaging pharmaceuticals, medical instruments, shrink tubing, corrosion- and weather-resistant laminates for wood and metal, cable sheathing, monofilaments for manufacturing filter cloth.

Applications-2
- Piezo and pyroelectric films for hydrophones, infrared detectors, respiration monitors, muscle sensors and security equipment.
- Modification of the relatively stiff homopolymer has resulted in more flexible grades thus opening up new applications. The melting range of the modified material is 162 to l65°C.

Melamine Resins

MELAMINE - FORMALDEHYDE 
Preparation of Melamine 
- A number of methods of producing melamine have been described. 
1. Heating dicyanodiamide, either with ammonia or on its own under  pressure.
2. Fusion of dicyanodiamide with a guanidine salt. 
3. From urea.
- Melamine, a non-hygroscopic, white crystalline solid, melts with decomposition above 347°C and sublimes at temperatures below the melting point. 

MANUFACTURE MELAMINE FORMALDEHYDE 
-  In a typical process a jacketed still fitted with a stirrer and reflux ‘condenser is charged with 240 parts 37% w/w formalin and the pH adjusted to 8.0-8.5 using sodium carbonate solution with the aid of a pH meter. 
- 126 parts of melamine (to give a melamine formaldehyde ratio of 1:3) are charged into the reactor and the temperature raised to 85°C.
- The melamine goes into solution and forms methylol derivatives 

Manufacture of Urea and Melamine Formaldehyde Resins
CURING OF MELAMINE FORMALDEHYDE RESIN
- Reaction of melamine with neutralised formaldehyde at about 80-100°C leads to the production of mixture of water-soluble methylolmelamines. 
- The principal resinification reaction involves methylol-methylol condensations. - Methylene links may also be formed by the following reactions.
Cross linked structure of melamine formaldehyde
MELAMINE FORMALDEHYDE MOULDING POWDERS
- MF moulding powders are prepared by methods similar to those used with UF material. 
- In typical process aqueous syrup, containing resin with a MF molar ratio of 1:2 is compounded with fillers, pigments, lubricants, stabilizers and in some cases accelerators in a dough-type mixer.
- The product is then dried and ball-milled.
- Magnesium carbonate is employed to act as a pH stabilizer during storage
- Decorative moulding powders a - cellulose is used as filler. 
- Industrial grade materials employ fillers such as asbestos, silica and glass fibre 

Mouldings from MF powders are superior to the UF plastics in a number of respects 
- Lower water absorption, especially with mineral-filled resins. 
- Better resistant to staining by aqueous solutions such as fruit juices and beverages. 
- Electrical properties, which are initially similar to those of UF resins, are maintained better in damp conditions and at elevated temperatures. 
- Better heat resistance. 
- Greater hardness. 
- MF moulding materials are more expensive than general purpose UF and PF resins. 
- MF is transparent 

GENERAL PROPERTIES 
- High surface hardness and scratch resistance, 
- High surface gloss, 
- High resistance to creep, 
- Resistance to heat (up to 250 °C for special grades), 
- Resistance to moisture, 
- Not suitable for continuous contact with boiling water, 
- High shrinkage as for UF moulding compounds, tendency to crack formation, 
- Curing properties better than UF moulding compounds, 
- Grades, which are free of smell, are permitted for the manufacture of utensils for food contact applications. 

CHEMICAL PROPERTIES
Resistances to Chemicals
- Fundamentally the Melamine formaldehyde mouldings are more resistants to solvents, oils, fats, weak acids and alkaline solutions than UF mouldings. 
Weathering Resistance
- Under high humidity conditions MF is having less water absorption than UF. However the water absorption depends on the nature of filler used in the composition. The weathered surfaces bleach and turn grey with micro cracks
Resistance to High Energy Radiation
- The radiation resistance of cellulose reinforced MF moulding compounds is the same as that of PF resins and special UF grade 

Flammability
- MF mouldings burn with a yellow flame and are self extinguishing on removal of source of ignition.  The combustion products have a choking smell of amines (fishy) and formaldehyde 
Toxicological Assessment
Special grades are permitted for food contact.  The special conditions are summarized below:
Behaviour in boiling test:   The boiling water must not be coloured or turbid.
Freedom from taste or smell:  The taste and smell of the water used for boiling is not allowed to differ from that of the control. 
Formaldehyde Release: More than 3 ppm of formaldehyde release is not allowed.

PROCESSING OF MELAMINE 
FORMALDEHYDE COMPOUNDS
Compression and Transfer moulding
- MF based compositions are easily moulded in conventional  compression and transfer moulding equipment. 
- A 3.2 mm thick moulding required about 190 seconds cure time at 150ºC but shorter times are possible with preheated powder.
- An interesting use of melamine resins in compression moulding involves decorative foils. A printed or decorated grade of paper is impregnated with resin and dried. 
- During compression moulding of MF, shortly before the cure is completed the mould is opened and the foil is placed in position and the resin in the foil cured in the position so that the foil actually bonds on the moulding.

Injection moulding
- Injection moulding of MF moulding powder is carried out on  a small scale. The temperatures are somewhat higher than UF. The barrel temperatures 100-115ºC; the mould temperatures 163-177ºC.
- Cure time employed depends on the properties required for the finished product 
AVAILABILITY
- Melamine moulding compounds are available as power, fibers, chips or granules.
 
TYPICAL APPLICATION
Principal application of melamine - formaldehyde moulding compositions is for the manufacture of tableware, largely because of their wide colouration range, surface hardness and stain resistance.
- Cellulose-filled compositions also find a small outlet for trays, clock cases and radio cabinets and other purposes. 
- Mineral­ filled powders are used in electrical applications and knobs and handles for kitchen utensils. 

Laminates Containing Melamine-Formaldehyde Resin 
- Use of laminates prepared using only melamine resins as the bonding agent is, however, limited to some electrical applications because of the comparatively high cost of the resin compared with that of P-F resins   
- Very large quantity of decorative laminates are produced in which the surface layers are impregnated with melamine resins and the base layers with phenolic resins 
- Their availability in a wide range of colours has led to their well-known applications in table tops and as interior wall-cladding in public buildings and public transport vehicles. 
- Glass-reinforced melamine-formaldehyde laminates are valuable because of their good heat resistance coupled with good electrical insulation properties; including resistance to tracking. 

Miscellaneous Applications 
- MF is now widely used in conjunction with urea (and formaldehyde) to produce adhesives of good strength, reactivity and water resistance 
- MF condensates are also useful in textile finishing 
Example : Useful agents for permanent glazing, rot proofing, wool  shrinkage control and, in conjunction with phosphorus compounds, flame proofing water repellence.

Urea Resins

UREA RESINS:
HISTORICAL DEVELOPMENT
- Among the various amino plastics, Urea and Melamine formaldehyde resins are the most important commercially 
- The interest in amino plastics dates from the publication of a patent by John in 1918 
- In 1926, as a result of work by E.C. Rossiter, moulding powders based on urea-thiourea-formaldehyde were marketed.  
- In 1935 Henkel patented, the production of resins based on melamine. Today these resins are important in the manufacture of decorative laminates and in tableware.
- The bulk of the amino resins are used in the woodworking industry 

UREA – FORMALDEHYDE RESINS
Preparation of Urea
- Urea is prepared by the reaction of liquid carbon dioxide and ammonia in silver-lined autoclaves, at temperature in the range 135-195ºC and pressure of 70-230 atm.
- Urea is a white crystalline compound with a melting point of 132.6ºC and is highly soluble in water.
Preparation of Formaldehyde
- As in the case of phenolic resin, formalin with both high and low methanol content is used to prepare formaldehyde.

MANUFACTURE OF UREA FORMALDEHYDE RESINS:
- Urea-formaldehyde ratios normally employed are in the range 1: 1.3 to 1: 1.5 
- Urea-formaldehyde resins are manufactured by a two-stage reaction. 
- First stage of resin preparation is to dissolve urea into the 36% w/w formalin which has been adjusted to a pH of 8 with caustic soda.
- Solution at the end of the first stage process contains urea, formaldehyde, and mono- and dimethylol urea 

Manufacture of Urea and Melamine Formaldehyde Resins
CURING OF UREA-FORMALDEHYDE RESINS
- Product of the first stage, contains unreacted urea and formaldehyde, is then subjected to acid conditions at elevated temperatures during the second stage. 
- In the first part of the second-stage methylol ureas condense with each other by reaction of an –CH2OH group of one molecule with an –NH2 group.
- More soluble resins produced on continuation of the reaction contain pendant methylol groups formed by reactions of the  groups with free formaldehyde - I
- Furthermore the ether linkages on heating may break down to methylene linkages with the evolution of formaldehyde
- These methylol groups and the methylol groups on the chain ends of the initial reaction product can then react with other methylol groups to give either linkages or with amine groups to give methylene linkages.
- When reactions II and III occur on average more than twice per molecule the resin gels, and cross-linking may be considered to have occurred. 

UREA FORMALDEHYDE mouldING MATERIAL
Compounding Ingredients 
Fillers
- Bleached wood pulp is employed for the widest range of bright colours and in slightly translucent mouldings,
- Woodflour, which is significantly cheaper, also be used.
Pigments
- A wide variety of pigments is now used in U-F moulding compositions 
Accelerator
- In order to obtain a sufficient rate of cure at moulding temperatures it is usual to add about 0.2-2.0% of a 'hardener' (accelerator). 
- This functions by decomposing at moulding temperatures to give an acidic body that will accelerate the cure rate. 
Example :- Ammonium sulphamate, ammonium phenoxyacetate, ethylene sulphite and trimethyl phosphate.
Stabilizer
- Urea-formaldehyde powders have a limited shelf-life but some improvement is made by incorporating a stabiliser such as hexamine into the moulding power 
Plasticizers
- Their main virtue is that they enable more highly condensed resins to be used and thus reduce curing shrinkage whilst maintaining good flow properties. 
- Glyceryl a - tolyl ether (monocresyl glycidyl ether) is often used for this purpose.
Lubricants
- Metal stearates such as zinc, magnesium or aluminium stearates are commonly used as lubricants at about I % concentration 

Compounding of moulding Compositions 
- Urea-formaldehyde is mixed with the filler (usually with a dry weight resin-filler ratio of about 2:1) and other ingredients except pigment in a tough mixer. 
- Resulting wet base is then fed to a drier which may be either of the turbine or rotary type. 
- On emerging from the drier the base is hammer-milled and then ball-milled.
- For densification the powder is heated as it passes along a belt and to drop the heated powder into the nip of a two-roll mill, 
In this process the material passes directly through the rolls to form a strip which is then hammer milled to give powder.
- More recent processes involve the use of continuous compounders, such as the Buss Ko-Kneader.

STRUCTURE AND GENERAL PROPERTIES
- The structure of the pre-condensate is a short chain molecule combined with CH2 bridges. 
- Low cost. The cheaper grades are sometimes lower in weight cost than the general purposes phenolics. (It is to be noted that urea formaldehyde have a somewhat higher density). 
- Wide colour range. 
- They do not impart taste and odour to foodstuffs and beverages with which they come in contact. 
- Good electrical insulation properties with particularly good resistance to tracking. 
Resistance to continuous heat up to a temperature of 70℃.

PHYSICAL PROPERTIES
Mechanical Properties
- UF and MF are the hardest of all plastic materials. 
- UF has a hardness of M-110 to 120 and MF of M-115 to 125 Rockwell Scale. 
- Although they are brittle at normal room temperatures,  UF and MF compounds exhibit very high modulus of elasticity 
Thermal Properties
- UF the continuous service temperature is 77ºC and for MF is 99ºC. 
- Heat deformation temperature (HDT)under load (1.8 MPa) is 130ºC for UF whereas HDT of MF is 183ºC. 
Optical Properties
- UF and MF resins are transparent
- Colour possibilities of both the materials are unlimited.

CHEMICAL PROPERTIES
Resistance to chemicals
- UF resins are resistant to solvents, oils, fats, weak acids and alkalies. 
- They are not resistant to strong acids and alkaline solutions, boiling water, oxidizing and reducing agents. 
Weather Resistance
- On immersion in cold water, UF mouldings absorb more water than MF. 
- Wood flour filled UF compounds have less weathering effect than cellulose filled compounds. 
Resistance to High Energy Radiation
- Radiation resistance of UF resin is high.  In the case of moulding compounds the nature of the reinforcing materials is the deciding factor 
Flammability
- UF moulded materials burn with a yellow flame and are self-extinguishing
- The combustion products have a choking smell of amines (fishy) and formaldehyde.
Toxicological Assessment
- Only special grades of UF are permitted for contact with food.

AVAILABILITY 
- Although available as fine powders, UF moulding compounds are mainly available as granules.
TYPICAL APPLICATIONS
Adhesives
- UF resins are used as adhesives for the particle board, plywood and furniture industries 
- Interior decoration panelling is the major end use of the UF particle board and plywood. 
- As gap filling resins by incorporating plasticizers.

Moulding compounds
- The first big application of UF resin is the moulding area. 
- The bulks of these applications are for plugs, sockets and switches switch box, plugs, sockets, lamp holders, screw cap for cosmetics, hair drier housings, table mats, telephone sets and cookware handles etc.