1973
DOI: 10.1515/hfsg.1973.27.4.126
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Determination of Cu-Cr-As and Zn in Preserved Wood by Atomic Absorption Spectroscopy

Abstract: The determination by atomic absorption spectroscopy of copper, chromium, arsenic (CCA) and zinc in treated pine and eucalypt wood is described. Oxidative treatment of shavings with 3.3 M HC1 in the presence of H 2 O 2 solubilizes the fixed components in 2 min at ioo°Cj the components then diffuse into the diluted extract in 10 to 20 min. The Cu, Cr, As, Zn in the extract are determined after filtration. The retention range of CCA-Zn in wood tested was 1.9 to 19 kg m~3. Overall errors for single determinations … Show more

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Cited by 10 publications
(7 citation statements)
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“…The procedure was essentially that described by Johanson (1974) for karri sleeper samples except that the first extraction was heated to ioo°C and held for 16 h at room temperature. Arsenic was determined by atomic absorption spectroscopy (Johanson 1973).…”
Section: Determination Of Arsenicmentioning
confidence: 99%
“…The procedure was essentially that described by Johanson (1974) for karri sleeper samples except that the first extraction was heated to ioo°C and held for 16 h at room temperature. Arsenic was determined by atomic absorption spectroscopy (Johanson 1973).…”
Section: Determination Of Arsenicmentioning
confidence: 99%
“…The reagents, the standard CCA-Zn stock solution and the AAS analysis procedure of test solutions were those described (Johanson 1973). …”
Section: Experimental (I) the Instrument And Reagentsmentioning
confidence: 99%
“…The procedure previously described for the determination of copper, chromium, arsenic and zinc in CCA-Zn preserved wood (Johanson 1973) is based on oxidativeextraction with dilute HC1. Although the method enables accurate and rapid determination of the metals by atomic absorption spectroscopy (AAS), in some situations organic extractives may interfere and cast doubt on the values.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…*) The analytical errors for arsenic values shown are within the ± 5°0 range and those for copper within the ±3% range loo ml aliquots were solubilised with HC1 and H £ O 2 and analysed by atomic absorption spcctroscopy as described previously (Johanson 1973). The difference between total and soluble arsenic was taken to represent insoluble arsenic.…”
Section: Introductionmentioning
confidence: 99%