1950
DOI: 10.1021/ac60045a050
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CRYSTALLOGRAPHIC DATA. 36. Cyclotetramethylene Tetranitramine (HMX)

Abstract: VOLUME 2 2, -NO. 9, SEPTEMBER 1950 1225 comparable chemical analyses. Direct comparison with the amount evaporated was not possible because of the absorption during the necessary mixing period in the closed room.The results deviate, on the average, by 8.3% from the amount found chemically, with the spectrometer low in five out of the seven cases.Although this accuracy is sufficient for many studies in industrial hygiene, particularly when conventional methods are not suitable because of the complexity of t… Show more

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Cited by 78 publications
(47 citation statements)
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“…In addition, a very small number of crystals exhibited a bulky prismatic habit with (101) faces very small and sometimes absent. The morphology of the last were similar to those described by McCrone [8] and by Palmer and Field [9]. Typically the smaller crystals were 6 mm along the longest dimension, although several larger crystals up to a maximum size of 21×10×8 mm 3 were also obtained.…”
Section: Resultssupporting
confidence: 80%
See 1 more Smart Citation
“…In addition, a very small number of crystals exhibited a bulky prismatic habit with (101) faces very small and sometimes absent. The morphology of the last were similar to those described by McCrone [8] and by Palmer and Field [9]. Typically the smaller crystals were 6 mm along the longest dimension, although several larger crystals up to a maximum size of 21×10×8 mm 3 were also obtained.…”
Section: Resultssupporting
confidence: 80%
“…McCrone [8] obtained massive crystals exhibiting forms {110}, {011}, and {101} by crystallization from acetic acid, acetone, nitric acid and nitromethane. As part of their studies on mechanical deformation of β-HMX, Palmer and Field [9] grew crystals with typical dimensions 5×5×3 mm 3 by solvent evaporation from acetone solution.…”
Section: Introductionmentioning
confidence: 99%
“…HMX exists in four solid phase polymorphs, labeled α, β, γ, and δ-HMX [9], each of which can be prepared by a specific cooling rate of the reaction solution [10]. The phase conversion of the β phase (monoclinic lattice structure) to the δ phase (hexagonal lattice structure) involves a major disruption of the crystal lattice and a ring conformation change long-term storage.…”
Section: Introductionmentioning
confidence: 99%
“…The polymorphic forms of HMX are well reported in the literature [5]. The ␤ polymorph of HMX is reported to exist in chair conformation while that of ␣, ␥ and ␦ phases exist in chair-chair conformation [6].…”
Section: Introductionmentioning
confidence: 74%