Explosive double salts and preparation. [Patent application] (open access)

Explosive double salts and preparation. [Patent application]

A new composition of matter has been discovered which is an explosive addition compound of ammonium nitrate (AN) and diethylenetriamine trinitrate (DETN) in a 50:50 molar ratio. the compound is stable over extended periods of time only at temperatures higher than 46/sup 0/C, decomposing to a fine-grained eutectic mixture (which is also believed to be new) of AN and DETN at temperatures lower than 46/sup 0/C. The compound of the invention has an x-ray density of 1.61 g/cm/sup 3/, explodes to form essentially only gaseous products, has higher detonation properties (i.e., detonation velocity and pressure) than those of any mechanical mixture having the same density and composition as the compound of the invention, is a quite insensitive explosive material, can be cast at temperatures attainable by high pressure steam, and is prepared from inexpensive ingredients. Methods of preparing the compound and the fine-grained eutectic composition of the invention are given.
Date: February 3, 1982
Creator: Cady, H. H. & Lee, K. Y.
System: The UNT Digital Library
Process for recovering rhenium from an alloy thereof (open access)

Process for recovering rhenium from an alloy thereof

Rhenium is recovered from an alloy containing that metal and either one or both of the metals molybdenum and tungsten by the following steps: (1) heating the alloy in the presence of O/sub 2/ to remove the Re from the alloy as gaseous Re/sub 2/O/sub 7/; (2) condensing the gaseous Re/sub 2/O/sub 7/; (3) dissolving the obtained solid Re/sub 2/O/sub 7/ in H/sub 2/O; (4) treating the solution of Re/sub 2/O/sub 7/ and H/sub 2/O with KCl to form KReO/sub 4/; and (5) heating the KReO/sub 4/ in the presence of H/sub 2/ to form Re.
Date: February 3, 1982
Creator: Heshmatpour, Bahman & McDonald, Robert E.
System: The UNT Digital Library
New prodrugs based on phospholipid-nucleoside conjugates (open access)

New prodrugs based on phospholipid-nucleoside conjugates

A method is described for the preparation of defined, isomerically pure phospholipid-nucleoside conjugates as a prodrug in which the drug (araC) is attached to the phospholipid by a monophosphate linkage. Key intermediates in the process involve selective blocking and deblocking of the nucleoside derivative. These particular monophosphate-linked derivatives represent a new class of prodrug, which are useful by themselves or in combination with diphosphate linked derivatives. Several new compositions involving diphosphate linked derivatives are described in which the products are isomerically pure and having defined fatty acid chain lengths.
Date: February 3, 1982
Creator: MacCoss, M.
System: The UNT Digital Library