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Patent No. 5307162

Cloaking System Using Optoelectronically Controlled Camouflage

A Cloaking System designed to operate in the visible light spectrum, utilizes optoelectronics and/or photonic components to conceal an object within it.

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Attorney: Sanders; John M.


Number of patents: 18
Last date: May 31, 1994

NumberTitleIssue Date
5316943Racemic conversion of using a transaminase
Recombinant cells and an improved method utilizing them is disclosed for the preparation of an optically pure, L-amino acid from its D and D,L isomer forms. The process utilizes cell cultures that possess high aminotransferase activity that exhibits moder...
05/31/1994
5229158Polyhydroxyalkanoate cream substitutes
Macrocolloids of polyhydroxyalkanoates are used as fat substitutes. Polyhydroxybutyrate is the preferred homopolymer. The polymeric particles can have a particle size of from 0.1-10 microns....
07/20/1993
5225227Polyhydroxyalkanoate flavor delivery system
Polyhydroxyalkanoates are combined with fat soluble flavors to provide a flavor delivery system for low-fat and no-fat foods. The polyhydroxyalkanoates preferably have a porous structure....
07/06/1993
5143741Concentrated, substantially non-aggregated casein micelles as a fat/cream substitute and a method for reducing the fat content in food products
Substantially non-aggregated casein micelles are employed as a fat substitute in food products. The concentrated casein micelles can replace all or a portion of the fat or cream in food products such as frozen dairy desserts, icings, puddings, whipped top...
09/01/1992
5112956Method for extraction of lipids and cholesterol
The present invention relates to a method for the removal of lipids and cholesterol from protein materials comprising the steps of (a) treating the protein with an extraction mixture comprising a lower alcohol, water and an acid, in concentrations selecte...
05/12/1992
4911946Carbohydrate cream substitute
A fat substitute is disclosed which comprises water-dispersable macro-colloid particles having a substantially spheroidal shape and a particle size distribution effective to impart substantially smooth organoleptic character of an oil-and-water emulsion. ...
03/27/1990
4900740N,N'-disubstituted guanidines containing a carboxyl or a tetrazolyl moiety
N,N'-disubstituted guanidines containing a tetrazolyl or glycine moiety are provided as high potency sweetening agents....
02/13/1990
4892820Solvent system for enzymatic coupling process
Alkylphosphate solvents are disclosed for use in an amino acid and amino acid ester enzymatic coupling process. ଱-Aspartylphenylalanine methyl ester and intermediates thereof are prepared enzymatically in an alkylphosphate solvent or cosolvent....
01/09/1990
4447257Inhibiting the antagonism between pyridyloxy-phenoxy alkanoate herbicides and benzothiadiazinone herbicides in post-emergent applications
The addition of crop oil to herbicidal compositions containing pyridyloxy-phenoxy alkanoate herbicides and benzothiadiazinone herbicides inhibits the antagonism between the pyridyloxy-phenoxy alkanoate herbicides and the benzothiadiazinone herbicides....
05/08/1984
4419453Immunological agglutination assays with dyed or colored latex and kits
Latex agglutination test methods and kits. Employing dyed latex polymer particles and adding a water-soluble, non-latex polymer particle absorbing dye contrasting in color to the dyed latex polymer particles produces a reaction mixture that changes color ...
12/06/1983
4387058Carbamic acid derivatives
Novel phenyl and naphthyl esters of 2-(1-oxo-alkoxy)ethyl carbamic acids are prepared. The compounds are useful as pharmacological and agricultural agents....
06/07/1983
4380649Isophorone derivatives
Novel isophorone derivatives are disclosed and possess utility as insect sterilants, plant growth regulators and fungicides....
04/19/1983
4356309N-Alkylated 2-(2-pyridyl)imidazoles useful as metallurgical extractants
Compounds of the formula ##STR1## wherein R1 represents C1 to C20 alkyl-substituted benzyl, or C2 to C20 alkyl which can optionally bear one or two --OR2 radicals, wherein each R2...
10/26/1982
4336384Preparation of 4-amino-3,5,6-trichloropicolinic acid
In a new method of producing 4-amino-3,5,6-trichloropicolinic acid 3,4,5,6-tetrachloropicolinonitrile is reacted with ammonium hydroxide, preferably at about 130° C. to about 160° C. The free acid is precipitated upon acidification of the reaction mixtu...
06/22/1982
4329474Selective solvent extraction of symmetrical tetrachloropyridine
Sym-tet (2,3,5,6-tetrachloropyridine) is selectively extracted from a reaction mixture comprising sym-tet, iodide ions and an aprotic solvent by contacting an extractant solvent with the reaction mixture. The extractant solvent is an alkane having at leas...
05/11/1982
4322538Preparation of symmetrical tetrachloropyridine
Symmetrical tetrachloropyridine (2,3,5,6-tetrachloropyridine) is prepared by reacting pentachloropyridine with a source of iodide ions in the presence of a proton source and a solvent medium. The reaction is preferably carried out in a polar, aprotic solv...
03/30/1982
4309440Substituted benzylidene methylhydrazides of acetic acid, their bactericidal and fungicidal use, and method of preparation
Substituted benzylidene methylhydrazides of haloacetic acid corresponding to the formula ##STR1## wherein R1, R2 and R3 each independently represent hydrogen, chloro or bromo with the proviso that at least one of R
01/05/1982
4306098Novel manufacture of 2,4,5-trichlorophenol
A method of producing 2,4,5-trichlorophenol with low levels of the impurity 2,3,7,8-tetrachlorodibenzo-.rho.-dioxin....
12/15/1981
 
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