Molecular orientation of PFPE lubricant films and its quantification

1997 ◽  
Vol 33 (5) ◽  
pp. 3118-3120 ◽  
Author(s):  
C. Gao ◽  
P. Dai
1998 ◽  
Vol 120 (2) ◽  
pp. 369-378 ◽  
Author(s):  
Chao Gao ◽  
Tam Vo ◽  
Joel Weiss

The objective of this paper is to demonstrate, from experiments and modeling, how and why molecular orientation of functional end groups of perfluoro-polyether (PFPE) lubricants play an important role in the tribological performance of thin film magnetic disks. These disks typically have an amorphous carbon overcoat upon which a thin lubricant layer is deposited using dip-coating technique. Glancing-angle FTIR (Fourier Transform Infra-Red Spectrometry) is used for measuring molecular orientation of planer functional end groups. A molecular orientation index (MOI) was defined as 1 for randomly oriented functional end groups. The MOI is mathematically derived as 3 (maximum) for lubricant molecules oriented with their functional end groups perpendicular to the surface, and as 0 (minimum) if lubricant molecules oriented with their functional end groups parallel to the surface. The MOI is shown to depend on processing conditions and lubricant film thickness. The tribological performance of the lubricant films was evaluated using drag-mode contact start-stop testing. It was found that wear durability of the lubricant films (~2 nm) with MOI ~ 1.5 is a few times better than those with MOI ~ 0.5 to 1.0. No significant difference in the amount of bonded lubricant film was detected over the range of MOI studied. Nor was there a detectable relationship with hydrophobicity. It was inferred from decreased MOI values due to thermal effects and storage time that a smaller MOI value corresponds to a lower free energy state of the lubricant film. Interestingly, MOI values for bonded lubricant films for Process A are found to be close to 3.0, suggesting that almost all functional end groups in the bonded films are oriented perpendicular to the carbon surface, close to 2.0 for process B, and close to 0 for process C, meaning that almost all functional end groups in the bonded films from process C are oriented parallel to the carbon surface. Relationship between physical/chemical bonding configurations and MOI values are graphically presented in detail. Based on this relation, a simple model on lubricant film structures for the three processes studied is presented. The model MOI values agree very well with measured MOI values as a function of lubricant thickness for all three processes, and the model also appears to account for the observed tribology performance for the MOI values studied (0.5 ~ 1.5).


Author(s):  
Norio Tagawa ◽  
Hiroshi Sendo ◽  
Atsunobu Mori

This paper describes the effects of molecularly thin liquid lubricant films on slider hysteresis phenomena of touch-down and take-off process in hard disk drives. In the experiments, the tested lubricants were conventional Zdol and novel cyclotriphosphazene-terminated PFPE lubricant (A20H lubricant) with different molecular weight. As a result, it is found that the difference between the touch-down velocity and take-off one (hysteresis behavior) for novel A20H lubricant film is larger than that for Zdol. The LDV RMS values for novel lubricant, which indicate the slider bouncing vibration during the slider-lubricant contact, are also larger than that for Zdol. The effects of lubricant film thickness and molecular weight on slider hysteresis behavior as well as slider bouncing vibration are also clarified. In addition, the replenishment performances of test lubricants for depleted tracks due to slider touch down contact are investigated and discussed.


2000 ◽  
Vol 123 (3) ◽  
pp. 533-540 ◽  
Author(s):  
Hiroshi Tani ◽  
Hiroyuki Matsumoto

The lubrication mechanism when the magnetic head is sliding on the magnetic disk in the drag test with cyclic interval rest periods, is discussed. A long rest period decreased the wear of disks and friction force. This result indicated that the reflow of lubricant into the contact areas decreased the wear of texture asperities. Next, the molecular spreading behavior of a lubricant film was calculated by Monte Carlo method to estimate the effect of lubricant recovering velocities. The lubricant replenishment into a thinner lubricant area made by an etching technique was measured. The measured profiles of lubricant replenishment were approximately agreed with the calculated profiles using a spreading model. It was clearly estimated that the reflow velocities changed in various cases of the environmental temperature, the radius of removal lubricant area, and the thickness of the lubricant films. Experimentally, the dependencies of temperature, the radius of removal lubricant area, and the lubricant thickness were measured in the drag test. This lubricant-spreading model adequately explained these results.


Author(s):  
Liling Cho ◽  
David L. Wetzel

Polarized infrared microscopy has been used for forensic purposes to differentiate among polymer fibers. Dichroism can be used to compare and discriminate between different polyester fibers, including those composed of polyethylene terephthalate that are frequently encountered during criminal casework. In the fiber manufacturering process, fibers are drawn to develop molecular orientation and crystallinity. Macromolecular chains are oriented with respect to the long axis of the fiber. It is desirable to determine the relationship between the molecular orientation and stretching properties. This is particularly useful on a single fiber basis. Polarized spectroscopic differences observed from a single fiber are proposed to reveal the extent of molecular orientation within that single fiber. In the work presented, we compared the dichroic ratio between unstretched and stretched polyester fibers, and the transition point between the two forms of the same fiber. These techniques were applied to different polyester fibers. A fiber stretching device was fabricated for use on the instrument (IRμs, Spectra-Tech) stage. Tension was applied with a micrometer screw until a “neck” was produced in the stretched fiber. Spectra were obtained from an area of 24×48 μm. A wire-grid polarizer was used between the source and the sample.


Author(s):  
Wendy Putnam ◽  
Christopher Viney

Liquid crystalline polymers (solutions or melts) can be spun into fibers and films that have a higher axial strength and stiffness than conventionally processed polymers. These superior properties are due to the spontaneous molecular extension and alignment that is characteristic of liquid crystalline phases. Much of the effort in processing conventional polymers goes into extending and aligning the chains, while, in liquid crystalline polymer processing, the primary microstructural rearrangement involves converting local molecular alignment into global molecular alignment. Unfortunately, the global alignment introduced by processing relaxes quickly upon cessation of shear, and the molecular orientation develops a periodic misalignment relative to the shear direction. The axial strength and stiffness are reduced by this relaxation.Clearly there is a need to solidify the liquid crystalline state (i.e. remove heat or solvent) before significant relaxation occurs. Several researchers have observed this relaxation, mainly in solutions of hydroxypropyl cellulose (HPC) because they are lyotropic under ambient conditions.


Sign in / Sign up

Export Citation Format

Share Document