scholarly journals Use of LDPE as matrix material in rubber sample preparation for IR analysis

1992 ◽  
Vol 11 (1) ◽  
pp. 3-11 ◽  
Author(s):  
S. Roy ◽  
P.P. De
1998 ◽  
Vol 71 (1) ◽  
pp. 17-25 ◽  
Author(s):  
M. Gerspacher ◽  
L. Nikiel ◽  
H. H. Yang ◽  
C. P. O'Farrell

Abstract A new method of measuring carbon black dispersion in rubber is presented. This method is based on the measurement of the light reflectivity from the rubber sample using standard equipment used in the evaluation of the tint strength of carbon black (ASTM D3265 procedure). This method can be applied for both uncured and cured samples; however, the uncured sample measurement has significant advantages in the simplicity of the sample preparation and obtaining important filler dispersion information of the compound. It is shown that samples with better dispersed carbon black reflect less light as compared to samples with poor carbon black dispersion.


1980 ◽  
Vol 34 (3) ◽  
pp. 314-319 ◽  
Author(s):  
D. Warren Vidrine

Fourier transform infrared spectroscopy of solids and liquids using photoacoustic detection is reported here. The advantages and disadvantages of photoacoustic detection are discussed, and comparisons of sample spectra obtained by different techniques, including photoacoustic detection, are presented and compared. Photoacoustic Fourier transform infrared spectroscopy is a promising spectroscopic method for IR analysis in cases where sample preparation is difficult.


Lubricants ◽  
2019 ◽  
Vol 7 (1) ◽  
pp. 4 ◽  
Author(s):  
Torrey Holland ◽  
Ali Mazin Abdul-Munaim ◽  
Dennis G. Watson ◽  
Poopalasingam Sivakumar

For the most reliable and reproducible results for calibration or general testing purposes of two immiscible liquids, such as water in engine oil, good emulsification is vital. This study explores the impact of emulsion quality on the Fourier transform infrared (FT-IR) spectroscopy calibration standards for measuring water contamination in used or in-service engine oil, in an attempt to strengthen the specific guidelines of ASTM International standards for sample preparation. By using different emulsification techniques and readily available laboratory equipment, this work is an attempt to establish the ideal sample preparation technique for reliability, repeatability, and reproducibility for FT-IR analysis while still considering the ease and efficiency of the technique. This study demonstrates that a stable emulsion within a sample, which depends heavily upon the method, provides a reliably consistent homogenous sample for quantification purposes with FT-IR analysis. Analysis of variance (ANOVA) modeling and limit of detection calculations demonstrate the stability of the emulsion. The results reveal that setting a mixing time for a calibration standard depends on the emulsification process. Inserting a probe directly into a sample (direct sonication) allows for a rapid, stable emulsion with high reproducibility. Indirect sonication produces relatively non-miscible liquids of different densities. The pan-shaker produces a reasonably stable emulsion, but without the long-term stability or quick production time of direct sonication. Reaction time plays a critical role in the rotary mixing method, which leads to a slow development of emulsification.


1988 ◽  
Vol 42 (7) ◽  
pp. 1239-1244 ◽  
Author(s):  
D. T. Durig ◽  
J. S. Esterle ◽  
T. J. Dickson ◽  
J. R. Durig

Woody peats from Indonesia and Malaysia were examined by FT-IR spectroscopy to observe the variation in degree of humification between peat types and among botanical components and matrix material within a peat type. Results of the FT-IR analysis showed significant changes occurring in the 1600 and 1000 cm−1 regions which are interpreted to represent lignin and lignocellulose, respectively. These components were considered to describe variations in degree of humification. Between peat types the intensity of the lignocellulose region decreased accordingly between fibric, hemic, and sapric samples. Within a sample, variations in the relative amount of lignocellulose in the three different size fractions of a sample were observed that could generally, but not always, be related to peat type. In all peat types the coarse material still contained some lignocellulosic component, whereas the finer fractions contained variably less to no lignocellulose. The lignin-dominated composition of the finer matrix material suggests that these peats are derived mainly from trees and woody vines with little input from herbaceous, less decay-resistant (cellulose-dominant) plant material.


Author(s):  
R. E. Ferrell ◽  
G. G. Paulson ◽  
C. W. Walker

Selected area electron diffraction (SAD) has been used successfully to determine crystal structures, identify traces of minerals in rocks, and characterize the phases formed during thermal treatment of micron-sized particles. There is an increased interest in the method because it has the potential capability of identifying micron-sized pollutants in air and water samples. This paper is a short review of the theory behind SAD and a discussion of the sample preparation employed for the analysis of multiple component environmental samples.


Author(s):  
T. J. Magee ◽  
J. Peng ◽  
J. Bean

Cadmium telluride has become increasingly important in a number of technological applications, particularly in the area of laser-optical components and solid state devices, Microstructural characterizations of the material have in the past been somewhat limited because of the lack of suitable sample preparation and thinning techniques. Utilizing a modified jet thinning apparatus and a potassium dichromate-sulfuric acid thinning solution, a procedure has now been developed for obtaining thin contamination-free samples for TEM examination.


Author(s):  
Earl R. Walter ◽  
Glen H. Bryant

With the development of soft, film forming latexes for use in paints and other coatings applications, it became desirable to develop new methods of sample preparation for latex particle size distribution studies with the electron microscope. Conventional latex sample preparation techniques were inadequate due to the pronounced tendency of these new soft latex particles to distort, flatten and fuse on the substrate when they dried. In order to avoid these complications and obtain electron micrographs of undistorted latex particles of soft resins, a freeze-dry, cold shadowing technique was developed. The method has now been used in our laboratory on a routine basis for several years.The cold shadowing is done in a specially constructed vacuum system, having a conventional mechanical fore pump and oil diffusion pump supplying vacuum. The system incorporates bellows type high vacuum valves to permit a prepump cycle and opening of the shadowing chamber without shutting down the oil diffusion pump. A baffeled sorption trap isolates the shadowing chamber from the pumps.


Sign in / Sign up

Export Citation Format

Share Document