Step 1: Define the thermal transitions for a semi-crystalline polymer as temperature increases.
- D. Glass transition temperature (Tg): This is the temperature at which the amorphous (non-crystalline) regions of the polymer change from a rigid, glassy state to a more flexible, rubbery state. This is the first major transition that occurs upon heating.
- B. Crystallization temperature (Tc): When an amorphous polymer is heated above its Tg, the polymer chains gain mobility. If held at a certain temperature, they can arrange themselves into ordered, crystalline structures. This process is called crystallization. On a DSC scan of a polymer being cooled from a melt, Tc is the peak where heat is released as crystals form. When heating an amorphous sample, it can also appear as an exothermic peak after Tg. It logically occurs after Tg but before melting.
- A. Melting temperature (Tm): This is the temperature at which the crystalline regions of the polymer melt and the material becomes a viscous liquid. This requires more energy than the glass transition, so Tm is always higher than Tg.
- C. Degradation temperature (Td): This is the temperature at which the polymer's chemical bonds begin to break, and the material starts to decompose. This is a chemical change, not a physical transition, and it occurs at a much higher temperature than melting.
Step 2: Arrange these temperatures in ascending (increasing) order. The sequence is: Glass Transition \(\rightarrow\) Crystallization \(\rightarrow\) Melting \(\rightarrow\) Degradation.
This corresponds to the order D, B, A, C.
The monomer used in the manufacture of Nylon 6 fiber is \(\underline{\hspace{2cm}}\)
The essential requirements of fiber forming polymers are \(\underline{\hspace{2cm}}\).
A. Linear polymer
B. Three dimensional polymer
C. High molecular weight
D. Strong lateral forces
Match the LIST-I (Spectroscopy) with LIST-II (Application)
LIST-I | LIST-II |
---|---|
A. Visible light spectroscopy | III. Identification on the basis of color |
B. Fluorescence spectroscopy | IV. Identification on the basis of fluorophore present |
C. FTIR spectroscopy | I. Identification on the basis of absorption in infrared region |
D. Mass Spectroscopy | II. Identification on the basis of m/z ion |
Match the LIST-I with LIST-II
LIST-I | LIST-II |
---|---|
A. Forensic Psychiatry | III. Behavioural pattern of criminal |
B. Forensic Engineering | IV. Origin of metallic fracture |
C. Forensic Odontology | I. Bite marks analysis |
D. Computer Forensics | II. Information derived from digital devices |
Match the LIST-I with LIST-II
LIST-I | LIST-II |
---|---|
A. Calvin Goddard | II. Forensic Ballistics |
B. Karl Landsteiner | III. Blood Grouping |
C. Albert Osborn | IV. Document examination |
D. Mathieu Orfila | I. Forensic Toxicology |
Match the LIST-I (Evidence, etc.) with LIST-II (Example, Construction etc.)
LIST-I | LIST-II |
---|---|
A. Biological evidence | IV. Blood |
B. Latent print evidence | III. Fingerprints |
C. Trace evidence | II. Soil |
D. Digital evidence | I. Cell phone records |
Match the LIST-I with LIST-II
LIST-I | LIST-II |
---|---|
A. Ridges | III. The raised portion of the friction skin of the fingers |
B. Type Lines | I. Two most inner ridges which start parallel, diverge and surround or tend to surround the pattern area |
C. Delta | IV. The ridge characteristics nearest to the point of divergence of type lines |
D. Enclosure | II. A single ridge bifurcates and reunites to enclose some space |