scholarly journals Simon Fraser University Radiocarbon Dates III

Radiocarbon ◽  
1984 ◽  
Vol 26 (3) ◽  
pp. 431-440 ◽  
Author(s):  
K A Hobson ◽  
D E Nelson

This list reports measurements made on archaeologic and geologic samples by our laboratory from June 1982 to December 1983. Results of measurements made during that period which lack review by submitters will be reported in a subsequent date list. Sample preparation techniques and benzene synthesis remain as described previously (R, 1982, v 24, p 344–351). For low organic samples, such as sediments, we now use a combustion tube assembly. These samples are burned under oxygen flow in a quartz tube. To absorb sulfur and break up nitrous compounds, we pass combustion gases through a 50% mixture of MnO2 and CuO wire heated to ca 500°C. The gas is then bubbled through a distilled water and KMnO4 solution to remove chlorides before being introduced into our standard dry ice and CO2 traps.

1995 ◽  
Vol 78 (3) ◽  
pp. 883-887 ◽  
Author(s):  
Elaine A Bunch ◽  
Diane M Altwein ◽  
Lloyd E Johnson ◽  
Joyce R Farley ◽  
Amy A Hammersmith

Abstract Sample homogeneity is critical to accurate and reproducible analysis of trace residues in foods. A method of uniform sample preparation using dry ice is described for shrimp. Other sample preparation techniques for raw shrimp produce nonhomogeneous samples. Sample homogeneity was determined through analysis of chloramphenicol added to intact tiger or white shrimp prior to sample preparation. Simulated chloramphenicol residue levels were 50, 15, 10, and 5 ppb. No significant differences were noted when analyses of shrimp inoculated with chlor-amphenicol prior to sample preparation with dry ice were compared with analyses of shrimp spiked after grinding with dry ice. Grinding shrimp with dry ice produced samples with homogeneous chloramphenicol residues. This technique should be applicable to other tissues and vegetable products.


Radiocarbon ◽  
1986 ◽  
Vol 28 (3) ◽  
pp. 1200-1205 ◽  
Author(s):  
Cecilio Gonzalez-Gomez ◽  
Purificacion Sanchez-Sanchez ◽  
Elena Villafranca-Sanchez

The following list includes some measurements made from December 1982 to May 1985 in the Radiocarbon Dating Laboratory, Faculty of Science, University of Granada, of samples from Spain, Portugal, and the Sudan. Sample preparation techniques and benzene synthesis remain as described previously (R, 1982, v 24, p 217–221) and equipment and measurement of samples was also reported previously (R, 1985, v 27, p 610–615). Radiocarbon ages are calculated using the 14C half-life of 5570 years and 0.95 activity of NBS oxalic acid is used as modern standard. Sample descriptions are based on information provided by submitters. Age determinations were made with the help of Research Project 0925/81, CAICYT, Spain.


Radiocarbon ◽  
1988 ◽  
Vol 30 (3) ◽  
pp. 341-346 ◽  
Author(s):  
Jinadasa Katupotha

Geologic samples for 14C age measurements were collected from the west, southwest and south coasts of Sri Lanka during October and November 1986. Sample points were leveled based on the Colombo datum level. Results presented below were obtained by liquid scintillation counting of methanol for coral and shell samples. Ages were measured from December 1986 to May 1987, at the Department of Geography, Hiroshima University, Radiocarbon Dating Laboratory, using the laboratory procedure described by Fujiwara and Nakata (1984). Sample preparation techniques were similar to those mentioned in the first list (Katupotha, 1988). The results are expressed in radiocarbon years relative to ad 1950 based on the Libby half-life of 5568 ± 30 years, using the new oxalic acid standard (SRM 4900C) as ‘modern’ (Stuiver, 1983).


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.


Author(s):  
M. John Hicks

Acid-etching of enamel surfaces has been performed routinely to bond adhesive resin materials to sound dental enamel as a caries-preventive measure. The effect of fluoride pretreatment on acid-etching of enamel has been reported to produce inconsistent and unsatisfactory etching patterns. The failure to obtain an adequate etch has been postulated to be due to fluoride precipitation products deposited on the enamel surface. The purpose of this study was to evaluate the effects of fluoride pretreatment on acid-etching of carieslike lesions of human dental enamel.Caries-like lesions of enamel were created in vitro on human molar and premolar teeth. The teeth were divided into two fluoride treatment groups. The specimens were exposed for 4 minutes to either a 2% Sodium Fluoride (NaF) solution or a 10% Stannous Fluoride (SnF2) solution. The specimens were then washed in deionized-distilled water. Each tooth was sectioned into four test regions. This was carried out to compare the effects of various time exposures (0 to 2 minutes) and differing concentrations (10 to 60% w/w) of phosphoric acid (H3PO4) on etching of caries-like lesions. Standard preparation techniques for SEM were performed on the specimens.


Author(s):  
P. B. Basham ◽  
H. L. Tsai

The use of transmission electron microscopy (TEM) to support process development of advanced microelectronic devices is often challenged by a large amount of samples submitted from wafer fabrication areas and specific-spot analysis. Improving the TEM sample preparation techniques for a fast turnaround time is critical in order to provide a timely support for customers and improve the utilization of TEM. For the specific-area sample preparation, a technique which can be easily prepared with the least amount of effort is preferred. For these reasons, we have developed several techniques which have greatly facilitated the TEM sample preparation.For specific-area analysis, the use of a copper grid with a small hole is found to be very useful. With this small-hole grid technique, TEM sample preparation can be proceeded by well-established conventional methods. The sample is first polished to the area of interest, which is then carefully positioned inside the hole. This polished side is placed against the grid by epoxy Fig. 1 is an optical image of a TEM cross-section after dimpling to light transmission.


Author(s):  
Ng Sea Chooi ◽  
Chor Theam Hock ◽  
Ma Choo Thye ◽  
Khoo Poh Tshin ◽  
Dan Bockelman

Abstract Trends in the packaging of semiconductors are towards miniaturization and high functionality. The package-on-package(PoP) with increasing demands is beneficial in cost and space saving. The main failure mechanisms associated with PoP technology, including open joints and warpage, have created a lot of challenges for Assembly and Failure Analysis (FA). This paper outlines the sample preparation process steps to overcome the challenges to enable successful failure analysis and optical probing.


Author(s):  
Jason H. Lagar ◽  
Rudolf A. Sia

Abstract Most Wafer Level Chip Scale Package (WLCSP) units returned by customers for failure analysis are mounted on PCB modules with an epoxy underfill coating. The biggest challenge in failure analysis is the sample preparation to remove the WLCSP device from the PCB without inducing any mechanical defect. This includes the removal of the underfill material to enable further electrical verification and fault isolation analysis. This paper discusses the evaluations conducted in establishing the WLCSP demounting process and removal of the epoxy underfill coating. Combinations of different sample preparation techniques and physical failure analysis steps were evaluated. The established process enabled the electrical verification, fault isolation and further destructive analysis of WLCSP customer returns mounted on PCB and with an epoxy underfill coating material. This paper will also showcase some actual full failure analysis of WLCSP customer returns where the established process played a vital role in finding the failure mechanism.


Author(s):  
Hyoung H. Kang ◽  
Michael A. Gribelyuk ◽  
Oliver D. Patterson ◽  
Steven B. Herschbein ◽  
Corey Senowitz

Abstract Cross-sectional style transmission electron microscopy (TEM) sample preparation techniques by DualBeam (SEM/FIB) systems are widely used in both laboratory and manufacturing lines with either in-situ or ex-situ lift out methods. By contrast, however, the plan view TEM sample has only been prepared in the laboratory environment, and only after breaking the wafer. This paper introduces a novel methodology for in-line, plan view TEM sample preparation at the 300mm wafer level that does not require breaking the wafer. It also presents the benefit of the technique on electrically short defects. The methodology of thin lamella TEM sample preparation for plan view work in two different tool configurations is also presented. The detailed procedure of thin lamella sample preparation is also described. In-line, full wafer plan view (S)TEM provides a quick turn around solution for defect analysis in the manufacturing line.


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