Abstract: The present disclosure concerns a process and a system for the electrochemical reduction of oxalic acid to glyoxylic acid. The process involves withdrawing a portion of oxalic acid-depleted catholyte from the process and contacting it with a quantity of solid oxalic acid to provide a concentrated oxalic acid solution which is re-entered into the process.

Abstract: A process for treating a dicarboxylic acid composition, with the proviso that the dicarboxylic acid is not furan 2,5-dicarboxylic acid, which process comprises: —introducing a dicarboxylic acid composition, which dicarboxylic acid composition contains an impurity compound and which impurity compound is an organic compound comprising a carbonyl group, into a cathode compartment of an electrochemical cell; and electrochemically reducing the impurity compound in the cathode compartment.

Abstract: Reduced glutathione is produced by a process for producing reduced glutathione by electroreduction of oxidized glutathione using a cathode cell and an anode cell separated from each other by a separating membrane, comprising using, as a solution in the cathode cell, an aqueous oxidized glutathione solution having a pH adjusted to higher than 3.0 and not more than 7.0 by adding a base, in which oxidized glutathione itself also acts as a conducting agent.

Abstract: The present disclosure is a method and system for production of oxalic acid and oxalic acid reduction products. The production of oxalic acid and oxalic acid reduction products may include the electrochemical conversion of CO2 to oxalate and oxalic acid. The method and system for production of oxalic acid and oxalic acid reduction products may further include the acidification of oxalate to oxalic acid, the purification of oxalic acid and the hydrogenation of oxalic acid to produce oxalic acid reduction products.

Abstract: Methods and systems for electrochemical conversion of carbon dioxide to carboxylic acids, glycols, and carboxylates are disclosed. A method may include, but is not limited to, steps (A) to (D). Step (A) may introduce water to a first compartment of an electrochemical cell. The first compartment may include an anode. Step (B) may introduce carbon dioxide to a second compartment of the electrochemical cell. The second compartment may include a solution of an electrolyte and a cathode. Step (C) may apply an electrical potential between the anode and the cathode in the electrochemical cell sufficient to reduce the carbon dioxide to a carboxylic acid intermediate. Step (D) may contact the carboxylic acid intermediate with hydrogen to produce a reaction product.

Abstract: The present disclosure is a system and method for producing a first product from a first region of an electrochemical cell having a cathode and a second product from a second region of the electrochemical cell having an anode. The method may include the step of contacting the first region of the electrochemical cell with a catholyte comprising an alcohol and carbon dioxide. Another step of the method may include contacting the second region of the electrochemical cell with an anolyte comprising the alcohol. Further, the method may include a step of applying an electrical potential between the anode and the cathode sufficient to produce a first product recoverable from the first region and a second product recoverable from the second region.

Abstract: An electrochemical cell having a cation-conductive ceramic membrane and an acidic anolyte. Generally, the cell includes a catholyte compartment and an anolyte compartment that are separated by a cation-conductive membrane. While the catholyte compartment houses a primary cathode, the anolyte compartment houses an anode and a secondary cathode. In some cases, a current is passed through the electrodes to cause the secondary cathode to evolve hydrogen gas. In other cases, a current is passed between the electrodes to cause the secondary cathode to evolve hydroxyl ions and hydrogen gas. In still other cases, hydrogen peroxide is channeled between the secondary cathode and the membrane to form hydroxyl ions. In yet other cases, the cell includes a diffusion membrane disposed between the secondary cathode and the anode. In each of the aforementioned cases, the cell functions to maintain the pH of a fluid contacting the membrane at an acceptably high level.

Abstract: An electrode substrate comprising M(n+1)AXn, where M is a metal of group IIIB, IVB, VB, VIB or VIII of the periodic table of elements or a combination thereof, A is an element of group IIIA, IVA, VA or VIA of the periodic table of elements or a combination thereof, X is carbon, nitrogen or a combination thereof, where n is 1, 2, or 3; and b) an electrocatalytic coating deposited on said electrode substrate, said coating being selected from at least one of b.1) a metal oxide and/or metal sulfide comprising ByC(1?y)Oz1Sz2, wherein B is at least one of ruthenium, platinum, rhodium, palladium, iridium, and cobalt, C is at least one valve metal, y is 0.4-0.9, 0<=z1, z2<=2 and z1+z2=2; b.2) a metal oxide comprising BfCgDhEi, wherein B is at least one of ruthenium, platinum, rhodium, palladium, and cobalt, C is at least one valve metal, D is iridium, E is Mo and/or W, wherein f is 0-0.25 or 0.35-1, g is 0-1, h is 0-1, i is 0-1, wherein f+g+h+i=1; b.3) at least one noble metal; b.

Abstract: The selective electrochemical reduction of halogenated 4-aminopicolinic acids is improved by activating the cathode in the presence of the starting material, excess alkali metal hydroxide and an alkali metal chloride, bromide or sulfate.

Abstract: A process for the preparation of ?-substituted carboxylic acids from the series including ?-hydroxycarboxylic acids and N-substituted-?-aminocarboxylic acids by cathodic carboxylation with carbon dioxide of a compound corresponding to the general formula R1—C(?X)R2 which is constituted by aldehydes, ketones or N-substituted imines. In the past, that carboxylation has taken place in an undivided electrolytic cell with the use of a sacrificial anode. As described herein, the carboxylation takes place in the absence of a sacrificial anode in an electrolytic cell divided by a separator, at a diamond film cathode. The anode is formed of a material which is stable under electrolytic conditions; in particular, it is a diamond film electrode. The catholyte includes an organic solvent and a conducting salt.

Abstract: A floral transport apparatus to facilitate the transportation and delivery of floral arrangements is disclosed. The floral transport apparatus includes a hard plastic container housing a support carriage having a set of longitudinal elastic bands and a set of lateral elastic bands stretched tightly over a box frame to form an upper and lower mesh. The floral arrangement is held securely in the gaps between the tensioned bands of the upper and lower mesh to prevent lateral displacement which would otherwise result in tipping of the floral arrangement. The floral transport apparatus provides a means for carrying many floral arrangements of various sizes simultaneously. Moreover, the floral transport apparatus is easily portable and manageable by a single delivery person and can be washed to keep the apparatus attractive in view of floral customers and potential floral customers.

Abstract: A cathode is made of an electrically conducting support with a coating of electrochemically deposited lead with a density between 0.001 and 2 g/cm3.

Abstract: A process for the production of 2-hydroxy-4-methylmercaptobutyric acid (MHA) by electrochemical carboxylation of 3-methylmercapto-propionaldehyde in an undivided electrolytic cell containing a sacrificial anode, in an aprotic solvent in the presence of a supporting electrolyte. Preferred anode/cathode combinations are Mg/Mg and Mg/carbon. MHA is obtainable in a high yield.

Abstract: A process for the preparation of chiral 2-aryl or 2-heterocyclyl-propionic acids of the formula wherein the substituents are as defined in the specification.

Abstract: One embodiment of the present invention provides a process, which includes:

Abstract: A process is described for preparing 3-exomethylene cephalosporanic acid derivatives for use in the synthesis of cephalosporin antibiotics such as ceftibuten. The process comprises electrochemical reduction of a compound of the formula (IV) ##STR1## wherein: R.sup.3 is CH.sub.3 C(O)--; ##STR2## is an optional sulfoxide group; n is 2 or 3; R.sup.1 is H and R is H or NHR.sup.2, where R.sup.2 is H or a protecting group selected from C.sub.6 H.sub.5 CH.sub.2 OC(O)--, C.sub.6 H.sub.5 C(O)-- or C.sub.1 -C.sub.6 alkoxy-C(O)--; or wherein R and R.sup.1 together with the carbon atom to which they are attached comprise --C(O)--, and produces the desired 3-exomethylene compounds with low levels of the corresponding 3-methyl tautomers.