Showing posts with label CHAPTER2. Show all posts
Showing posts with label CHAPTER2. Show all posts

Friday, August 8, 2008

Water Absorption

2.8 WATER ABSORPTION (ASTM D 570):

The tendency of plastics to absorb moisture simply cannot be overlooked since even the slight amount of water can significantly alter some key mechanical, electrical, or optical property. Water absorption characteristic of plastics depend largely upon the basic type and the final composition of the material. For example, materials containing only hydrogen and carbon, such as polyethylene and polystyrene, are extremely water resistant, where as plastics having oxygen or oxy-hydrogen groups are very susceptible to water absorption. Cellulose acetate and nylons are good example of the preceding type. Materials containing chlorine, bromine, or fluorine are water repellent. Fluorocarbon, such as PTFE, is one such type of water repellent material. Water absorption characteristics of plastic material are altered by the addition of additives such as fillers, glass fibers, and plasticizers. These additives show a greater affinity to water, especially when they are exposed to the outer surface of the molded article. Some plastics absorb very little water at room temperature, but at higher temperatures that tend to take in a considerable amount of water and loose properties rapidly. Washing machine agitator, plastic dinnerware, irrigation valves, and sprinklers are examples of application requiring low water absorption.

2.8.1 PROCEDURE:

The test to determine water absorption of plastics is relatively simple. Only two equipments are required, an analytical balance and an oven capable of maintaining a uniform temperature. The test specimen may be molded disc or a piece cut from a sheet, rod, or tube. Dimensions vary according to the type of specimen. A special conditioning procedure must be followed before actual testing. The specimens are dried in an oven at a specified temperature for a predetermined time, cooled in a desiccator, and immediately weighed. The percent increase in weight during immersion is calculated as follows:

Increase in weight percent = ( Wet Weight- Conditioned Weight) * 100 / Conditioned Weight

2.6 IMPACT PROPETIES

2.6 IMPACT PROPETIES:

2.6.1 INTRODUCTION:

The impact properties of the polymeric materials are directly related to the overall toughness of the material. Toughness is defined as the ability of the polymer to absorb applied energy. The area under the stress strain curve is directly proportional to the toughness of the material. The higher the impact energy of the material, the higher the toughness of the material and vice versa. Impact resistance is the ability of a material to resist breaking under a shock loading or the ability to resist the fracture under stress applied at high speed. The theory behind toughness and brittleness of the polymers is very complex and therefore difficult to understand. The molecular flexibility plays an important role in determining the relative brittleness of toughness of the material. For example, in stiff polymers like polystyrene and acrylics, the molecular segment are unable to disentangle and respect to the rapid application of mechanical stress and the impact produces brittle failure. In contrast, flexible polymers such as plasticized vinyls have high impact behavior due to the ability of the large segment of molecules to disentangle and respond rapidly to mechanical stress.

Impact properties of the polymer are often modified simply by adding an impact modifier such as butadiene rubber of certain acrylic polymers. The addition of a plasticizer also improves the impact behavior at the cost of rigidity. Another way to improve impact properties is to use fibrous fillers that appear to act as stress transfer agent. Most polymers when subjected to the impact loading seem to fracture in a characteristic fashion. The crack is initiated on a polymer surface due to the impact loading. The energy required to initiate such a crack is called the crack initiation energy. If the load exceeds beyond the crack initiation energy then crack continue to propagate. A complete failure occurs when the energy applied goes beyond the crack propagation energy. Thus, both crack initiation as well as the crack propagation contributes to the impact property measurement. There are four types of failure mode when material is given an impact load[2,12].

BRITTLE FAILURE: In this type of failure, the part fractures extensively with out yielding. A catastrophic mechanical failure such as the one in the general-purpose polystyrene is observed.

SLIGHT CRACKING: the part shows slight cracking and yielding with out losing its shape or integrity.

YIELDING: The part actually yields showing obvious deformation and stress whitening but no cracking-taking place.

DUCTILE FAILURE: This type of failure is characterized by a definite yielding of material along with cracking. Polycarbonate is considered a ductile material.

Impact properties are one of the wildly specified mechanical properties of the polymeric materials. However, it is also one of the least understood properties. Predicting the impact resistance of polymers remains one of the most troublesome areas of product design. One of the with some earlier Izod and Charpy impact tests was that the tests were adopted by the plastic industry from metallurgist. The principles of impact mechanism as applied to metals do not seem to work satisfactorily with plastic because of the plastic complex structure.

2.6.2 TYPES OF IMPACT TESTS:

In the last decade, tremendous amount of money and time has been spent on the research and development of various type of impact test by organization throughout the world. Attempts have been made to develop different sizes and shape of specimen as well as impact tester. The specimens have been subjected to a variety of impact loads including tensile, compression, flexural and torsion impacts. Impact loading has been applied using every thing from and hammer, punches, and pendulums of falling balls and bullets. Unfortunately, very little correlation exists, if any between the types of tests developed so far. Numerous technical papers and articles have been written on the subject of the advantage of one method over other. To this date, no industry wide consensus exists regarding an ideal impact test method. Impact testing is divided in to three major classes and subdivided in to several classes as follows,

Classification of Impact Testing

Organization Chart


Fig. 2.4 Classification of Impact Testing

PENDULUM IMPACT TEST:

IZOD IMPACT TEST (ASTM D-256)

Izod Specimen Positioning

fig 2.5 Izod Specimen Positioning

The objective of the above test is to measure the relative susceptibility of a standard specimen to the pendulum type impact loading. The results are expressed in terms of kinetic energy consumed by the pendulum in order to break the specimen. The energy required to break a standard specimen is actually the sum of energies needed to deform it, to initiate its fracture, and to propagate the fracture across it, and the energy expended in tossing the broken ends of specimen. This is called “toss factor”. The energy lost through the friction and vibration of the equipment is minimum for all practical application and usually neglected.

The specimen used in Izod test must be notched. The reason behind notching the specimen is to generate a stress concentration area that promotes a brittle rather than a ductile failure. A plastic deformation is prevented in the specimen by the presence of a notch. The impact values are severally affected because of the notch sensitivity of a certain plastic material. The Izod test requires a specimen to be clamped vertically as a cantilever beam. The specimen is struck by a swing of a pendulum released from a fixed clamp from the specimen clamp.

CHARPY IMPACT TEST (ASTM D-4812):

Charpy Specimen Positioning

fig 2.6 Charpy Specimen Positioning

This test is conducted in a very similar manner to the Izod impact strength test. The only difference is the positioning of the specimen. In the test the specimen is mounted horizontally and supported unclamped at both ends. Only the specimen that breaks completely is considered acceptable. The Charpy impact strength is calculated by dividing the indicator reading by the thickness of the specimen. The results are reported in (feet-lbf/inch) of the specimen. The obvious advantage of the of the Charpy test over the Izod test is that the specimen does not have to be clamped and, therefore, it is free of variation in clamping pressure.

APPARTUS AND TEST SPECIMEN:

Impact Testing Machine

fig 2.7 Impact Testing Machine

The testing machine consisting of a heavy base with a vise for clamping the specimen in place during the test. In most of cases, the vise is designed so that the specimen can be clamped vertically for the Izod test or positioned horizontally for the Charpy test with out making any changes. A pendulum type hammer with an antifriction bearing is used. Additionally weights may be attached to the hammer for breaking tougher specimens. The pendulum is connected to a pointer and a dial mechanism that indicates the excess energy remaining in a pendulum after breaking the specimen. The dial is calibrated to read the impact values directly in inch. A hardened steel striking nose is attached to the pendulum. The Izod and Charpy test use different types of striking noses. The test specimen can be prepared either by molding or by cutting them from sheets. Izod test specimen are 2 ½ * ½ *1/8 (inch). A notch is cut into a specimen very carefully by a milling machine or a lathe. The recommended notch depth is 0.1 inch.

TEST PROCEDURE:

The test specimen is clamped into positioning so that the notched end of the specimen is facing the striking edge of the pendulum. The pendulum hammer is released, allowed to strike the specimen, and swing through. If the specimen does not break more weight is added to the hammer and test is repeated until failure occurs. The impact values are directly read from the scale. The impact values are calculated by dividing the impact values obtained from the scale by the thickness of the specimen. The reverse notch impact resistance is obtained by reversing the position of the notched specimen in the vise. In the case, the notch is subjected to compressive rather than tensile stress during impact.

Notching the specimen drastically reduces the energy loss due to deformation, and hence it can be neglected. Tough plastic material that have an Izod impact higher than .5 (feet-lb/inch) of notch seem to expand very little energy in tossing the broken end of the specimen.

2.6.3 EFFECT OF TEST VARIBLES AND LIMITATION:

NOTCH:

A slight variation in the radius and depth of a notch affects the impact strength results. Many other variables such as the cutter speed, sharpness of the cutting tooth, feed rate, type of plastic, and quality of the notch cutting equipment all seem to have a significant effect on the results. Such a variation is difficult to control and non-uniformity between the lots is quite common. Certain heat sensitive polymers are also affected by the high cutter speed that seems to contribute to the thermal degradation. The notch in the specimen tends to create a stress concentration area that produces unrealistically low impact values in crystalline plastics. Recommendations include, even time interval between notching and testing and waiting at least 40 hours after notching and before testing.

SPECIMEN THICKNESS:

Although the impact values reported are based on 1-inch thickness specimen, the actual thickness of the specimen used in the test influences the test results. This is especially in the case of polycarbonate.

SPECIMEN PREPARATION:

Injection molded specimens seem to yield higher impact strength values than compression molded specimens. This is due to the molecular orientation caused by the injection molding process. The location of the gate also has a significance effect on the test specimen’s results, particularly in the case of fiber-reinforced specimens.

TEMPERATURE:

Impact values increases with increase in the temperature and vice versa.

FILLERS AND OTHER ADDITIVES:

Fillers and reinforcements have pronounced effect on the test results. Fillers and reinforcement agents generally lower the impact values.

2.6.4 LIMITATION:

The results obtained from Izod and Charpy method cannot be directly used for part design these results does not give the true energy required to break the specimen. The notched Izod impact test measures only the notch sensitivity of the different polymers and not the toughness.

2.7 FLEXURAL PROPERTIES (ASTM D-790):

2.7.1 INTRODUCTION:

The stress strain behavior of polymers in flexure is of interest to a designer as well as a polymer manufacturer. Flexural strength is the ability of the material to with stand bending forces applied perpendicular to its longitudinal axis. The stress induced by the flexural load is a combination of compressive and tensile stresses. Flexural properties are reported and calculated in terms of the maximum stress and strain that occurs at the outside surface of the test bar. Many polymers do not break under flexure even after a large deflection that makes deformation of the ultimate flexural strength impractical for many polymers. In such cases, the common practice is to report flexural yield strength when the maximum strain in the outer fiber or the specimen has reached 5 percent. For polymeric materials that break easily under flexural load, the specimen is deflected until rupture occurs in the outer fibers.

There are several advantages of flexural strength tests over tensile tests. If a material is used in the form of a beam and if the service failure occurs in the bending, then a flexural test is more relevant for a design or specification purpose than a tensile test, which may give strength value very different from the calculated strength of the outer fiber in the bent beam. The flexural specimen is comparatively easy to prepare with out residual strain. The specimen alignment is also difficult in the case of a tensile test. Also the tight clamping of specimen in tensile create stress raising points. One other advantage of the flexural is that a small strain, the actual deformations are sufficiently large to be measured accurately.

Two basic methods cover the determination of flexural properties of the polymer. Method 1 is a three point loading utilizing center loading on a simple supported beam. A bar of rectangular cross section rests on two supports and it is loaded by means of a loading nose at the center. The maximum axial fiber stress occurs on a line under the loading nose. Method 2 is a four point loading system utilizing two load points equally spaced from their adjacent supporting points, with a distance between loading point of one third of the support span. In this test, the test bars lie on a two support and is loaded at two points each an equal distance from the adjacent support points. Either method can be used with the two procedures. Method1 is used for materials that break at comparatively low loads. Method2 is used particularly for those materials that undergo large deflections during testing. The basic difference between the two procedures is the strain rate. Method1 is .01 (inch/inch/min) and Method2 is .1(inch/inch/min).

2.7.2 APPARATUS:

Quiet often the machine used for tensile testing is also used for flexural testing. The upper or lower portion of the movable crosshead can be used for flexural testing. The dual-purpose load cell that indicates the load applied in the tension as well as compression facilitates testing of the specimen in either tension or compression. The machine used for this purpose should operate are a constant rate of cross head motion over the entire range and the error in the load measuring system should not exceed. The loading nose and support must have cylindrical surfaces. The radius of the nose and the nose support should be at least 1/8 inch. To avoid excessive indentation or failure due to stress concentration directly under the loading nose. A strain gauge type of mechanism called a deflectometer or a compression is used to measure deflection in the specimen.

2.7.3 TEST SPECIMEN AND CONDITIONING:

The specimen used for the flexural testing are bars of rectangular cross section and are cut from sheets, plates, or molded shapes. The common practice is to mold the specimen to the desired finish dimensions. The specimens are conditioned in accordance with the procedure A of ASTM methods D 618 as explained. The specimen of size 1/8 * ½ * 4(inch) are the most commonly used.

2.7.4 TEST PROCEDURE AND CALCULATION:

The test is initiated by applying the load to the specimen at the specified crosshead rate. The deflection is measured either by a gauge under the specimen in contact with it in the center of the support span or by measurement of the motion of the loading nose relative to the supports. A load deflection curve is plotted if the determination of flexural modulus value is desired. The fiber stress is related to the load and sample dimensions and is calculated using the following equation

Method 1 S = 3PL/2bd2

Where S= stress (psi), P= load (lb), L= length of span (in.), b=width of specimen (in.), d= thickness of specimen (in.).

Flexural strength is equal to maximum stress in the outer fibers at the moment of the break. This value can be calculated by using the above stress equation by letting load value P equal to the load at the moment of the break.

For materials that do not break at outer fiber strains up to 5 percent, the flexural yield strength is calculated using the same equation. The load value P in this case is the maximum load at which there is no longer an increase in load with an increase in deflection. The maximum strain of the fibers, which also occurs at mid span, is calculated using the following equation (method 1).

r = 6Dd/ L2

Where r = strain (in./in.), D = deflection (in.), L = length of the span (in.), d = thickness of the specimen (in.).

The equations for calculating maximum fiber stress and maximum fiber strain are slightly different in method 2.

2.7.5 FACTORS AFFECTING THE TEST RESULTS:

SPECIMEN PREPERATION:

The molecular orientation in the specimen has a significant effect on the test results. For example, the specimen with a high degree of molecular orientation perpendicular to the applied load will show higher flexural values than that of the specimen with orientation parallel to the applied load. The injection-molded specimen usually shows a higher flexural value than a compression-molded specimen does.

TEMPERATURE:

The flexural strength and modulus values are inversely proportional to the temperature. At higher testing temperature, flexural strength and modulus values are significantly lower.

TEST CONDITIONS:

The strain rate, which depends upon testing speed, specimen thickness, and the distance between supports (span), can affect the results. At a give span a flexural strength increases as the specimen thickness is increased. The modulus of the material generally increases with increasing strain rate.

2.5 HARDNESS TEST

2.5 HARDNESS TEST:

2.5.1 INTRODUCTION:

Hardness is defined as the resistance of the material to deformation, particularly permanent deformation, indentation, or scratching. Hardness is purely a relative term and should not be confused with wear and abrasion resistance of the plastic material. Polystyrene, for example have very high Rockwell hardness but have very poor abrasion resistance. Hardness tests can differentiate the relative hardness of different grades of particular plastic. However, it is not valid to compare the hardness of various plastic entirely based on one type of test, since elastic recovery along with hardness is involved. The test is further complicated by the phenomena of creep. Many tests have been devised to measure the hardness. Because plastic materials vary considerably with respect to hardness, one type of hardness test does not cover the entire range of hardness property encountered. Two of the most commonly used hardness test for plastic is Rockwell and the Durometer hardness test. The Rockwell test is applied for relatively hard plastics such as acetals, nylons, acrylic, and polystyrene. For softer materials like flexible PVC, thermoplastic rubber, and polyethylene, durometer hardness is used.

2.5.2 DUROMETER HARDNESS: (ASTM D 2240)

The test method is based on the penetration of a specified indentor forced in to the material under specified conditions. Two types of durometer are commonly used Type A and Type D. the basic difference between the two type is the shape and dimension of the indentor. The hardness number derived from either scale is just numbers with out any units. Type A durometer is used with relatively soft materials while Type D durometer is used widely with harder materials[2,12].

2.5.3 APPARATUS:

The durometer hardness tester consists of a pressure foot, an indentor, and an indicating device. The indentor is a spring-loaded device and the point of the indentor protrudes through the hole in the base. The basic difference between the two types is the shape and the dimension of the indentor. The test specimen is at least ¼ in inch thick and can be either moulded or cut from a sheet. The poor contact between the thin specimens may cause the result to vary considerably.

Hardness Testing Machine 2Hardness Testing Machine 1

fig 2.2 Hardness Testing Machine fig 2.3 Durometer

2.5.4 PROCEDURE:

  1. The test is carried out by first placing a specimen on a hard, flat surface.
  2. The pressure foot of the instrument is pressed on to the specimen, making sure that it is parallel to the surface of the specimen.
  3. The durometer hardness is read with 1 sec after the pressure foot is in firm contact with the specimen.
  4. The readings are noted at various places and the average value is taken.

2.5.5 FACTORS AFFECTING THE TEST RESULTS:

TEMEPRATURE AND HUMIDITY:

The hardness of all the plastic material is directly affected by the changes in the temperature and humidity. Specimen tested at higher than specified temperature tends to indicate a lower value.

SURFACE CONDITION OF THE SPECIMEN:

The surface finishes of the specimen have high significance on the results obtained. A smooth surface yields a higher value than a machined surface.

FILLER:

The hardness value may vary depending upon the type and the amount of filler present in the resin. The variation in hardness may be caused by the difference in hardness between resin and the filler.

ANISOTROPY:

Plastic with anisotropic property may cause indentation hardness to vary with the direction of testing.

2.4 TENSILE TESTING (ASTM D638)

2.4 TENSILE TESTING (ASTM D638):

2.4.1 INTRODUCTION:

A tensile test is also known as a tension test is probably one of the most fundamental mechanical tests that can be performed on a material. Tensile tests are simple, relatively inexpensive and determine how the material will react to the forces being applied in tension. Tensile test in board sense is the measurement of the ability of the material to withstand forces that tend to pull it apart and to what extent the material stretches before breaking. As the material is, being pulled you will find its strength along with how much it will elongate. Materials, which exhibit the largest strengths during tensile testing, have the lowest impact values. Tensile modulus is an indication of the relative stiffness of the material, and can be determined from the stress strain diagram. Many plastic are very sensitive to the rate of straining and environmental conditions. Therefore the data obtained from this method cannot be considered valid for applications involving load time scales or environmental widely different from this method. The tensile property data helps in preferential selection of a particular type of plastic from a large group of plastic material and such data are of limited use in actual design of the part. This is because the test does not take in to account the time dependent behavior of plastic material. As the pull of the material is continued until it breaks, a complete tensile profile is obtained. A curve will result showing how it reacts to the forces being applied. The point of failure is of much interest and is typically called its ultimate strength or “UTS” on the chart. Uniaxial tension test provides important information about the mechanical properties of the material[2,12].

2.4.2 SCOPE OF THE EXPERIMENT:

This test method covers determination of tensile properties of un reinforced and reinforced plastics in the form of standard dumbbell shaped specimen when tested under defined condition of pretreatment, temperature, humidity, and testing machine speed. This method can be used for testing materials of any thickness above 1.0mm to14mm. This test method includes the option of determining the Poisson’s ratio at room temperature. Test data obtained by this method are relevant and appropriate for use in engineering design.

2.4.3 SIGNIFICANCE AND USE:

This test method is designed to produce tensile property data for the control and specification of plastic materials. These data are also useful for qualitative characterization, research and development. It is advisable to refer to the material specification before using this test method. Tensile properties may vary with the specimen preparation in exactly the same way. Many plastics are very sensitive to the rate of straining and environmental conditions. Therefore the data obtained from this method cannot be considered valid for application involving load time scales or environmental widely different from this method. When uniaxial tensile force is applied to a solid, the solid stretches in the direction of the applied force but it also contracts in both directions lateral to the applied direction of force. If the solid is homogeneous and isotropic, the material remains elastic under the action of the applied force; the lateral strain bears a constant relationship to the axial strain. This constant is called poisons ratio, is defined as the negative ratio of the reverse to axial strain under uniaxial stress.

2.4.4 APPARATUS:

The tensile testing machine of a constant rate of cross head movement is used. It has a fixed or assembly stationary member carrying a second grip. Self-aligning grips employed for holding the test specimen between the fixed member and the movable member prevents alignment problems.

TENSILE TESTING (ASTM D638)

Fig.2.1 Universal Testing Machine

Driving mechanism: a controlled velocity drive mechanism is used. Some of the commercially available machines use a closed loop servo controlled drive mechanism to provide a high degree of accuracy.

Load indicator: a load indicating mechanism capable of indicating total tensile load with an accuracy of + 1% of the indicated value or better is used.

Extension indicator: An extension indicator commonly known as extensometer is used to determine the distance between the designated points located within the gauge length of the test specimen as it is stretched.

Micrometer: The advent of the new microprocessor technology has virtually eliminated the time consuming manual calculation. Stress, elongation, modulus, energy, statically calculation are performed automatically and presented on a visual display or hard copy print out at the end of test can be obtained.

2.4.5 TEST SPECIMEN:

The Type 1 specimen shall be used where sufficient material having a thickness of 7mm (.28in) or less is available. The Type 2 specimen may be used when a material does not break in a narrow section with the preferred Type 1 specimen. The Type 3 specimen must be used for all materials with a thickness of greater than 7mm (.28in) but more than 14mm (.55in). The Type 4 specimen are used when direct comparison is required between materials in different rigidity cases (that is, non-rigid and semi rigid). The Type 4 specimen shall be used for testing non - rigid plastics with a thickness of 4mm (.16in) or less. The Type 5 specimens may be used where only limited material having a thickness of 4mm (.16in) or less is available for evaluation, or where a large number of specimens are to be exposed in a limited space. The test specimen for reinforced composites, including highly orthotropic laminates, shall conform to the dimensions of the Type 1 specimen[2].

2.4.6 SPECIMEN PREPARATION:

The test specimen can be prepared by machining operation, or die cutting, from the materials in sheet, slab or similar form. Specimens can also be prepared by molding the material to be tested.

2.4.7 SPEED OF TESTING:

Speed of testing shall be relative ratios of the grips or test fixtures during the test. The rate of motion of the driven grip or fixture when the testing machine is running to idle may be used. Choose the speed of testing depending upon the type of material used.

2.4.8 CONDITIONING:

Condition the specimen at 23+/- 2o C and 50+/-5% relative humidity for not less than 40 hours prior to the test. Conduct the test at 23+/-2 o C and 50+/-5% relative humidity unless other wise specified by the contract or the relevant ASTM material specification.

2.4.9 PROCEDURE:

The speed of testing is the relative rate of motion of the grips or test fixture during the test fixture during the test. The test specimen is positioned vertically in the grips or test fixture during the test. The grips are tightened evenly and firmly to prevent any slippage. The speed of testing is set at the proper rate and the machine is started. As the specimen elongates, the resistance of the specimen increases and it is detected by the load cell. This load value is recorded by the instrument. The elongation of the specimen is continued until a rupture of the specimen is observed. Load value at break is also recorded. The tensile strength at yield and the tensile strength at break are calculated.

Tensile Strength = Force (lb) / Cross Section Area ( sq.in)

Tensile Strength at Yield = Maximum Load Recorded (lb) / Cross Section Area ( sq.in )

Tensile Strength at break = Load Recorded at break ( lb ) / Cross Section Area ( sq.in )

1. Mark off the units of stress in lb/in2 on the X-axis of the chart. This is done by dividing the force by cross section area of the specimen.

2. Mark off the units of strain in. /in. on the Y-axis. These values are obtained by dividing the chart value by the magnification selected.

3. Carefully draw a tangent KL to the initial straight-line portion of the stress-strain curve.

4. Select any two convenient points on the tangent.

5. Draw a straight line PQ and LM connecting points P and L with Y-axis of the chart.

6. Then the tensile values are calculated as follows.

Tensile Modulus = Difference in corresponding stress / Difference in corresponding strain

7. Elongation at yield,

Strain = Change in length (elongation) / Original length.

EXPERIMENTAL PROCEDURES

2.0 EXPERIMENTAL PROCEDURES:

2.1 MATERIAL DETAILS:

Matrix – HDPE

Supplier - Haldia Petrochemicals

Trade name - Halene – H, B 6401

Melt Flow Index (2.16 kg, 190°C) - 0.30 g / 10min

Density - 0.964 g / cm3

Melting temperature - 132 ° C

Calcium carbonate

Particle size - 2.25µm

LLDPE

Melt Flow Index (2.16 kg, 190°C) - 50

2.2 PREPARATION OF POLYEYHYLENE COMPOUNDS:

According to the formulation obtained from the design table of CCD, the calcium carbonate and LLDPE are mixed in five different levels of calcium carbonate namely 56, 60, 70, 80, and 84. The calcium carbonate is incorporated into the LLDPE matrix using a twin-screw extruder and the extrudate was pelletized. Then the masterbatch was mixed with HDPE matrix in five different let down ratios namely 1, 5, 15, 25, 29. From these mixtures (mixed by simple hand mixing) test samples were prepared using injection molding technique.

2.3 SPECIMEN PREPARATION TECHNIQUE:

The injection molding process is best suited for producing articles made up of thermoplastic materials. In injection molding, a definite quality of molten thermoplastic material is injected under pressure into a relatively cold mold where it solidifies into the shape of the mold.

The process consists of feeding the compounded plastic material as granules or powder through the hopper at definite time intervals into the hot horizontal cylinder where it gets softened. Pressure is applied through a hydraulically driven cylinder into a mold fitted at the end of the cylinder. While moving through the hot zone of the cylinder, the plastic material is uniformly spread around the inside wall of the cylinder thereby ensuring uniform heat distribution. The molten plastic material is then injected into the mold cavity. By using a mechanical locking device, the mold is properly held in position as the molten plastic material is injected under high pressure. Proper flow of the molten material to interior portions of the mold is achieved by preheating the mold to an appropriate temperature. After the mold has been filled with the molten material, it is cooled and then opened to eject the molded article[6].

Injection Moulding Machine

2.4 TENSILE TESTING (ASTM D638):

2.4.1 INTRODUCTION:

A tensile test is also known as a tension test is probably one of the most fundamental mechanical tests that can be performed on a material. Tensile tests are simple, relatively inexpensive and determine how the material will react to the forces being applied in tension. Tensile test in board sense is the measurement of the ability of the material to withstand forces that tend to pull it apart and to what extent the material stretches before breaking. As the material is, being pulled you will find its strength along with how much it will elongate. Materials, which exhibit the largest strengths during tensile testing, have the lowest impact values. Tensile modulus is an indication of the relative stiffness of the material, and can be determined from the stress strain diagram. Many plastic are very sensitive to the rate of straining and environmental conditions. Therefore the data obtained from this method cannot be considered valid for applications involving load time scales or environmental widely different from this method. The tensile property data helps in preferential selection of a particular type of plastic from a large group of plastic material and such data are of limited use in actual design of the part. This is because the test does not take in to account the time dependent behavior of plastic material. As the pull of the material is continued until it breaks, a complete tensile profile is obtained. A curve will result showing how it reacts to the forces being applied. The point of failure is of much interest and is typically called its ultimate strength or “UTS” on the chart. Uniaxial tension test provides important information about the mechanical properties of the material[2,12].

2.4.2 SCOPE OF THE EXPERIMENT:

This test method covers determination of tensile properties of un reinforced and reinforced plastics in the form of standard dumbbell shaped specimen when tested under defined condition of pretreatment, temperature, humidity, and testing machine speed. This method can be used for testing materials of any thickness above 1.0mm to14mm. This test method includes the option of determining the Poisson’s ratio at room temperature. Test data obtained by this method are relevant and appropriate for use in engineering design.

2.4.3 SIGNIFICANCE AND USE:

This test method is designed to produce tensile property data for the control and specification of plastic materials. These data are also useful for qualitative characterization, research and development. It is advisable to refer to the material specification before using this test method. Tensile properties may vary with the specimen preparation in exactly the same way. Many plastics are very sensitive to the rate of straining and environmental conditions. Therefore the data obtained from this method cannot be considered valid for application involving load time scales or environmental widely different from this method. When uniaxial tensile force is applied to a solid, the solid stretches in the direction of the applied force but it also contracts in both directions lateral to the applied direction of force. If the solid is homogeneous and isotropic, the material remains elastic under the action of the applied force; the lateral strain bears a constant relationship to the axial strain. This constant is called poisons ratio, is defined as the negative ratio of the reverse to axial strain under uniaxial stress.