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Crosslinked copolymers of .alpha.,.beta.-olefinically unsaturated dicarboxylic anhydrides |
| What is claimed is: 1. A crosslinked copolymer comprising the following copolymerized units: A. 2.0 ... |
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Effective hydrocarbon blend for removing asphaltenes from oil wells |
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Highly activated mixtures for constructing load bearing surfaces and method of making the same |
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Cycloaliphatic unsaturated ketones as odour- and taste-modifying agents |
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Certain fluorine substituted PGI.sub.2 compounds |
| What is claimed is: 1. A compound of the formulae: ##STR22## wherein Y, T, W and X may each be H or ... |
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Various 15-deoxy-16-hydroxy-16-ethynyl and 16-ethynylsubstituted prostaglandins |
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Tetrahydro-2-(nitromethylene)-2H-1,3-thiazines |
| I claim as my invention 1. A resonance hybrid in which the two significant forms which contribute ... |
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Pyrazolidinone salts as developing agents |
| We claim: 1. A 1-phenyl-3-pyrazolidinone salt of the formula ##STR14## in which X.sup..crclbar. is ... |
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Isotope separation process
| Details |
Inventors: Maas, Jr., Edward T.; Cox, Donald M.;
Assignee: Exxon Research & Engineering Co. (Florham Park, NJ)
Primary Examiner: Schafer; Richard E.
Assistant Examiner:
Attorney, Agent or Firm: Krumholz; Arnold H.
Processes are disclosed for the separation of isotopes of an element comprising vaporizing uranyl compounds having the formula (UO.sub.2 A.sub.2).sub.n, where A is a monovalent anion and n is an integer from 2 to 4, the compounds having an isotopically shifted infrared absorption spectrum associated with uranyl ions containing said element which is to be separated, and then irradiating the uranyl compound with infrared radiation which is preferentially absorbed by a molecular vibration of uranyl ions of the compound containing a predetermined isotope of that element so that excited molecules of the compound are provided which are enriched in the molecules of the compound containing that predetermined isotope, thus enabling separation of these excited molecules. The processes disclosed include separation of the excited molecules by irradiating under conditions such that the excited molecules dissociate, and also separating the excited molecules by a discrete separation step. The latter includes irradiating the excited molecules by a second infrared laser in order to convert the excited molecules into a separable product, or also by chemically converting the excited molecules, preferably by reaction with a gaseous reactant. |
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DETAILED DESCRIPTION The uranyl compounds including at least two isotopes of the element which is to be separated (for example uranium or oxygen) and having an isotopically shifted infrared absorption spectrum associated with the uranyl ions containing that element which are employed in connection with this invention have the general formula (UO. sub. 2 AA'). sub. n where A and A' are monovalent anions and n is an integer greater than 1, i. e. from 2 to 4. Where n is 2, 3 or 4, the dimer, trimer and tetramer, respectively are produced. Preferably, both A and A' will comprise the same anion, so that the general formula for the compounds useful in the process of this invention will be (UO. sub. 2 A. sub. 2). sub. n. In a preferred embodiment thereof A comprises 1,1,1,5,5,5-hexafluoroacetylacetonate (hfacac). The anions A and A' utilized in the uranyl ion-containing compounds utilized in the process of this invention are preferably selected so as to enhance the Lewis acidity of the complexed uranyl ion. For this reason it is found, for example, that more fluorinated species of anions generally tend to be more preferred for use therein. It is also preferred that these anions themselves have a minimum volatility, i. e. , such that they will boil, at pressures of about 1 atmosphere at temperatures of below about 200. degree. C. As is set forth in pending U. S. Application Ser. No. 961,363, filed on Nov. 16, 1978, the anions A and A' for use in these compounds of this process, when polydentate, thus forming a chelation ring around a part of their respective uranyl ions, must be such that these chelation rings will not open and bridge at the elevated temperatures at which these compounds are intended to be used. If these rings were to open and bridge with adjacent uranyl ions at lower temperature, there would at the very least be a severe reduction in their volatility. It is therefore preferred that these anions, A and A', have an atomic framework with a minimum length corresponding to that of the diketonate unit, so as to form relatively unstrained chelate rings
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