Eight Argonne Premium Coal samples and two other coal samples were used to observe the effects of combustion and leaching on 30 elements. The results were used to infer the modes of occurrence of these elements. Instrumental neutron activation analysis indicates that the effects of combustion and leaching on many elements varied markedly among the samples. As much as 90% of the selenium and bromine is volatilized from the bituminous coal samples, but substantially less is volatilized from the low-rank coals. We interpret the combustion and leaching behavior of these elements to indicate that they are associated with the organic fraction. Sodium, although nonvolatile, is ion-exchangeable in most samples, particularly in the low-rank coal samples where it is likely to be associated with the organic constituents. Potassium is primarily in an ion-exchangeable form in the Wyodak coal but is in HF-soluble phases (probably silicates) in most other samples. Cesium is in an unidentified HN03-soluble phase in most samples. Virtually all the strontium and barium in the low-rank coal samples is removed by NH4OAc followed by HC1, indicating that these elements probably occur in both organic and inorganic phases. Most tungsten and tantalum are in insoluble phases, perhaps as oxides or in organic association. Hafnium is generally insoluble, but as much as 65% is HF soluble, perhaps due to the presence of very fine grained or metamict zircon. We interpret the leaching behavior of uranium to indicate its occurrence in chelates and its association with silicates and with zircon. Most of the rare-earth elements (REE) and thorium appear to be associated with phosphates. Differences in textural relationships may account for some of the differences in leaching behavior of the REE among samples. Zinc occurs predominantly in sphalerite. Either the remaining elements occur in several different modes of occurrence (scandium, iron), or the leaching data are equivocal (arsenic, antimony, chromium, cobalt, and nickel). The results of these combustion and leaching experiments indicate that some previously held assumptions concerning modes of occurrence of elements in coal should be reconsidered.

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The mercury contents of 109 reference samples of 12 organizations have been determined by flameless atomic absorption spectrometry. The homogeneity of mercury in the six USGS samples issued in 1964 was tested twice, a year apart, using unopened bottles of samples. The analysis of variance of these data in the form of a design with a single variable of classification showed that the mercury contents of the 12 sets can be considered homogeneous at F0.95 and that 10 of these sets can be considered homogeneous at F0.90, a more stringent test. Data for other reference samples were generally obtained using Youden Squares. This experimental design was used so that we could determine the significance of the variation attributable to some cause on the days on which mercury was determined, to the order in which the determinations were made on the several days, and to the mercury contents of the samples in each design. For the latter, one may assume that the mercury contents of samples will differ and that a significant F ratio may be obtained. For the principal variable of classification, the variation attributable to some cause on the days on which mercury was determined was significant for only 1 of 9 analyses of variance of sets of data but we have not been able to explain the cause of the significance. The mercury contents of the several types of samples, except for micas, dunites, and perhaps the granodiorites, depend on the origin of the samples. The mercury contents of ande‐sites and basalts of continental origin are higher than those for similar samples originating in island arcs or the circum‐Pacific belt. We conclude that the high and extremely variable mercury content of W‐1 is probably due to mercury resulting from the use of mercury fulminate detonators in the quarry prior to the collection of the sample.

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