Lec. No. 2

Processing of glass fibers

All glass are derived from compositions containing sand, but it also includes varying quantities of feldspar, sodium sulfate, boric acid, and many other materials. In the glass melting furnace, the raw materials are heated to temperatures ranging from1500 to 1700°C and are transformed through a sequence of chemical reactions tomolten glass. In operation, raw materials are introduced continuously on top of a bed of molten glass, where they slowly mix and dissolve. Mixing is effected by natural convection, gases rising from chemical reactions, and, in some operations, by air injection into the bottom of the bed.

the molten glass is forced through heated platinum bushings containing numerous very smallopenings(d=(1-2) mm). The continuous fibers emerging from the openings are drawn over a roller applicator to produce diameter of fiber in the range (5-15µm . the choice degree of glass molten is depending on viscosity and temperature , the best temperature is upper from 100C°from liquid line according to phase diagram.

Furnace for glass melting

Lec . No . 3

Oxide fibers

Ceramic oxide fibers, both continuous and discontinuous, have beencommercially available since the 1970s, and processing and microstructurecontrol are very important in obtaining the desired properties. Among thedesirable characteristics in any ceramic fiber for structural applications are:

1) High theoretical density, i.e. low porosity

2) Small grain size for low-temperature applications

3) Large grain size for high-temperature applications

4)High purity.

1)Alumina fibers

Alumina fibers have γ, δ and α allotropic forms. α-Alumina is thethermodynamically stable form. In practice, it is very difficult to control thetime and temperature conditions to proceed from γ to α . At low firing, thefibers will give a smaller grain size and therefore an unacceptable level ofporosity. At higher processing temperatures, porosity can be eliminated butexcessive grain growth will result. This dilemma can be avoided by introducinga second phase that restricts grain boundary mobility while the porosity isremoved at high temperature. It is possible to select the type and amount ofthe second phase that inhibits the grain growth at the service temperature.

Lec. No.4

Whiskers

Whiskers are normally obtained by vapor phase growth. They are

monocrystalline, short fibers with extremely high strength because of theirhigh aspect ratio (50 to 10 000). They have a diameter of a few microns, butthey do not have uniform dimensions and properties. ceramic Whiskers produce from oxides : Al2O3 , MgO , MgO-Al2O3 , BeO , NiO , ZnO , Cr2O3.

ceramic Whiskers are produced from molten metal at air or wet hydrogen inert gas then pull and crystal growth at one direction . more Whiskers are used (Al2O3 , SiC).

table : properties of oxide whiskers

Material / S.G / Melting point / T.S(Gpa) / E(Gpa)
Al2O3 / 3.9 / 2082 / 14-28 / 550
BeO / 1.8 / 2549 / 14-21 / 700
B2O3 / 2.5 / 2449 / 7 / 450
MgO / 3.6 / 2799 / 7-14 / 310

Nano oxide fibers

An emerging technology is the production of fibers of very small diameter, of the orderof 50nm. These fibers are produced by the spinning of a precursor organic fiber from apipette to a collecting plate. A high voltage (tens of kilovolts) is passed between the pipetteand the plate and the polymer is drawn from the pipette to the plate. The fibers are generallycollected on the plate to form a random array although work is proceeding to align the fibers.

Lec. No.5

Non-oxide fibers

Commercially available non-oxide ceramic reinforcements are in three

categories: continuous, discontinuous, and whiskers. non-oxide fibers are used in different application at high and low temperature .Silicon carbide fiber is a major development in the field of ceramic reinforcements.

1. Silicon carbide

Continuous SiC fibers were produced by thermal degradation of a polymer precursor such as a polycarbosilane. to from a continuous fiber is made by melt-spinning. The fiber is then converted by pyrolysis at 1300°C into a fiber consisting mainly of(β-SiC) of about 15µm diameter.

Methods of manufacturing SiC fibers

1) SiCfibers via polymers

2)SiC fibers via CVD

2)boron carbide and boron nitride

There are other promising ceramic fibers, e.g. boron carbide and boron

nitride. Boron nitride fiber has the same density (2.2 g /cm3) as carbon fiber,but has a greater oxidation resistance and excellent dielectric properties.Boron carbide fiber is a very light and strong material.

Lec. No.6

Fibrous monolithic ceramics (FMs)

Fibrous monolithic ceramics (FMs) consist of a hexagonal arrangement of

submillimeter ‘cells’ of strong polycrystalline ceramic and a network of

crack-deflecting weak ‘cell boundaries’. These composites are sintered or hot-pressed monolithic ceramics with a distinct fibrous texture. This uniquearchitecture opened new avenues for ceramic composites, in which they failin a nonbrittle manner because of crack interactions with weak cell boundaries such as crack deflection or crack delamination . This approach provides simple and versatile method for manufacturing nonbrittle ceramic compositesfrom a variety of different material combinations that include oxide ceramicsAl2O3/Al2O3–ZrO2 and non-oxide ceramics (SiC/graphite), (SiC/BN ) and( Si3N4/BN).

three processing methods for producing fibrous monolithic ceramics, i.e. coextrusion, microfabrication by coextrusion , and hybrid extrusion and dip-coating .

Lec. No.7

Structures of Fibrous monolithic ceramics

Various material combinationsFibrous monolithic ceramics consist of dense cells separated by a continuouscell boundary, in which the cells provide most of the strength of the FM andthe cell boundary provides the toughness by isolating the cells from each other and promoting dissipation of fracture energy by mechanisms such aspullout of the cells or deflection of a crack through the cell boundary . The cell boundaries must be either weak themselves or poorly bonded to thecells to dissipate fracture energy and exhibit minimal or no reaction with thecells for long-term use at elevated temperatures. To date, many kinds of structural ceramics have been examined for a strong cell phase. They are inthe forms of either oxides (Al2O3, ZrO2 and ZrSiO4 ) or nonoxides (SiC , Si3N4 , and borides ). Oxides have the advantageof stability in oxidizing environments, while non-oxides have the advantageof substantially higher strength and superior creep resistance.

In all-oxide FMs, porous cell boundaries are generally employed because

Lec. No.8

SiC/SiC Composites

CMCs exhibit high mechanical properties at high or very high temperatures (400–3000°C), and in severe environments. They were developed initially for military andaerospace applications. Now they are being introduced into new fields and their rangeof applications will grow when their cost is lowered drastically.CMCs can be fabricated by different processing techniques, using either liquid orgaseous precursors. The CVI SiC/SiC composites consist of a SiC-based matrix reinforced

by SiC fibers. They are produced by Chemical Vapour Infiltration (CVI). This technique derives directly from Chemical Vapour Deposition. In very simpleterms, the SiC-based matrix is deposited from gaseous reactants on to a heated substrate offibrous preforms (SiC). CVI is a slow process, and the obtained composite materials possesssome residual porosity and density gradients. Despite these drawbacks, the CVI processpresents a few advantages:

(i) the strength of reinforcing fibers is not affected duringcomposite manufacture.

(ii) the nature of the deposited material can be changed easily,simply by introducing the appropriate gaseous precursors into the infiltration chamber.

(iii)a large number of components.

(iv) large complex shapes can be produced in a near netshape.

Lec. No.9

Interface properties – influence on the mechanical behavior

The fiber-matrix interfacial domain is a critical part of composites because load transfersfrom the matrix to the fiber and occur through the interface. Most authors promotethe concept of weak interfaces to increase fracture toughness. The major contribution totoughness is attributed to crack bridging and fiber pull-out. Weak interfaces are detrimentalto composite strength. A high strength requires efficient load transfers from fibers to thematrix. This is obtained with strong interfaces. These latter requirements, to be met for strong composites, aretherefore incompatible with the former ones for tough composites, if toughening is basedsolely upon the above mentioned weak interface-based mechanisms.Fiber/matrix interfaces exert a profound influence on the mechanical behavior andthe lifetime of composites. Efforts have been directed towards optimization of interfaceproperties.

(FIGURE. Schematic diagram showing crack deflection when the fiber coating/interface is strong (a) orweak (b))

Lec. No.10

Silicon Melt Infiltrated CeramicComposites(MI-CMCs)

Silicon melt infiltrated, SiC-based ceramic matrix composites (MI-CMCs) have beendeveloped for use in gas turbine engines. These materials are particularly suited to use ingas turbines due to their:

1) low porosity. 2) high thermal conductivity. 3) low thermal expansion. 4) high toughness. 5)high matrix cracking stress.

PROCESSING of (MI-CMC)

the term “melt infiltrated ceramic matrix composite” (MI-CMC) willrefer only to continuous fiber composites whose matrices are formed by molten silicon (orsilicon alloy) infiltration into a porous SiC- and/or C-containing preform. The process of (MI-CMC) includes :

1) As with most other ceramic composite systems, a coating is applied to the fibers to serveas the fiber-matrix interphase.

2) fibrous perform

a) In the prepreg process

b)In the slurry cast process

Some important thermal properties of Prepreg and Slurry Cast measured at room temperature and at 1200°C, are listed in Table 3. Overall, the thermal properties

Table 3

Lec. No.11

Fracture Strength

The in-plane tensile fracture response of materials are typically characterizedby a stress-strain curve as shown in Figure 2 when measured in a simple displacementcontrolledmethod. In general, the curve can be divided into four sections (shown bythe dotted lines in Figure 2), with the first section representing the simple linear elasticloading of the composite.

FIGURE 2. Typical in-plane tensile stress-strain behavior for a continuous fiber reinforced ceramic composite.

Lec. No.12

Carbon Fiber Reinforced Silicon Carbide Composites (C/SiC, C/C-SiC)

Ceramic matrix composites (CMC), based on reinforcements of carbon fibers andmatrices of silicon carbide (called C/SiC or C/C-SiC composites) represent a relativelynew class of structural materials. In the last few years new manufacturing processes andmaterials have been developed.

PROCESSING of (C/SiC, C/C-SiC)

Three different techniques are currentlyused in an industrial scale for the production of C/SiC and C/C-SiC composites, each ofthem leading to specific microstructures and properties :

1)Chemical Vapour Infiltration (CVI).

2)Liquid Polymer Infiltration (LPI) or Polymer Infiltration and Pyrolysis (PIP).

3)Liquid Silicon Infiltration (LSI).

Lec. No.13

Carbon fiber / carbon matrix composite (c/c composite)

Carbon fiber-reinforced carbon is a composite materialconsisting of carbon fiber reinforcement in a matrix of graphite . Carbon–carbon is well-suited to structural applications at high temperatures, or where thermal shock resistance and/or a low coefficient of thermal expansion is needed. While it is less brittlethan many other ceramics, it lacks impact resistance .carbon/Carbon (C/C) is a lightweight, high-strength composite material capable of withstanding temperatures over 3000°C in many environments.

Processing of (c/c composite)

The material is made in three stages:

First, material is laid up in its intended final shape, with carbon filament and/or cloth surrounded by an organicbinder such as plastic. Often, cokeor some other fine carbon aggregate is added to the binder mixture.

Second, the lay-up is heated, so that pyrolysis transforms the binder to relatively pure carbon.

Third, the voids are gradually filled by forcing a carbon-forming gas such as acetylene through the material at a high temperature, over the course of several days.