38 results about "Dithionite" patented technology

A method is provided for improving enzymatic hydrolysis in saccharification of a lignocellulosic material. The method is comprising pretreating the lignocellulosic material to obtain a slurry of pretreated lignocellulosic material; adding at least one reducing agent to the slurry of pretreated lignocellulosic material or the liquid fraction thereof to decrease the enzymatic hydrolysis inhibitory properties of slurry of the pretreated lignocellulosic material or the liquid fraction thereof; and subjecting the slurry of pretreated lignocellulosic material or the liquid fraction thereof to enzymatic hydrolysis in the presence of the at least one reducing agent.

A method for mitigating fouling in a wash unit used in a hydrocarbon cracking process wherein the fouling is due to the presence of polymers and deposits thereof formed by condensation of carbonyl compounds contained within a feed stream of the wash unit. In one embodiment, the invention provides a method of mitigating fouling in a wash unit by introducing into the feed stream an effective amount of an additive including: an inorganic salt of dithionite; and an epsilon caprolactam or a 6-amino caproic acid derivable therefrom. The additive scavenges the carbonyl compounds contained within the feed stream and dissolves deposits of the polymers to thereby mitigate fouling in the wash unit.

The invention relates to a method for removing films and deposits from stainless surfaces, especially from stainless metallic surfaces such as they are used in process stations and production units in the pharmaceutical, food and biotechnological industries, and to an aqueous cleaning solution comprising a reducing agent, in particular dithionite and / or disulfite, and at least two different complexing agents, wherein one of these complexing agents is a compound comprising diacetic acid groups or a salt thereof, for removing rouging on surfaces of stainless steels that come into contact with media selected from the group of chromium / nickel and chromium / nickel / molybdenum steels in the neutral pH range.

The invention provides a thiosulfate gold leaching method and application, and relates to the technical field of hydrometallurgy. The thiosulfate gold leaching method comprises the steps of adding metal salt, a polycarboxylic acid additive and thiosulfate into gold-containing ore pulp for leaching, wherein a large number of acid radical groups distributed on a hydrocarbon chain of the polycarboxylic acid additive and positive ions generated through hydrolysis of the metal salt in a solution can be subjected to a multi-tooth chelation effect to generate complex ions, thereby replacing Cu (NH3)4 < 2 + > in a traditional thiosulfate gold leaching process, and the defect of large thiosulfate consumption due to the fact that Cu (NH3) 4 < 2 + > has oxidability can be overcome on the premise that the high gold leaching rate is obtained. The concentration of harmful ions such as dithionite in decomposition products of S2O3 < 2-> in the leaching solution is remarkably reduced, and recycling ofthe leaching solution and recycling of gold in the solution are facilitated; and meanwhile, the thiosulfate gold leaching method also avoids the problems of safety and environmental influence causedby the use of ammonia water.

The invention relates to a method for treating refractory organic pollutants in wastewater by dithionite-activated persulfates, which comprises the following steps: sequentially adding a dithionite and a persulfate into wastewater containing therefractory organic pollutants, and conducting reacting to obtain treated wastewater, wherein the molar ratio of the persulfate to the refractory organic pollutants in the wastewater is 1:1 to 500:1. The method has the characteristics that the method is carried out under the conditions of normal temperature, normal pressure, acidity or neutrality, no external energy is used, the risk of secondary pollution to the environment is avoided, the operation is simple, the degradation effect on the refractory organic pollutants in the environment is good, and the method has great application potential in the field of environmental pollution treatment.

A linker system is provided where a small molecule reactive group, e.g., an activity based probe which binds to certain enzymes at the active site, is linked through an aryl diazo linker to an affinity molecule such as biotin. The reactive group may comprise a number of functionalities known to react with a specific target to be studied. This enables the probe to be exposed to analytes, such as proteins and bind specifically to them to form a complex having an affinity molecule allowing immobilization of the bound analyte on an affinity column or other support, e.g. with streptavidin. Then, the linker is cleaved without causing removal of the affinity group or dissociation of the probe from the analyte. The linker is cleaved under mild reducing conditions, e.g., dithionite. The probe is synthesized along with the linker on a solid support.

The present invention provides a method for decreasing the fermentation inhibition in a process for producing a target chemical from a pretreated cellulosic material, the process comprising enzymatic hydrolysis of the pretreated cellulosic material and fermentation of hydrolysed material, wherein the fermentation inhibitory properties of the material subjected to fermentation is decreased by an addition of at least one reducing agent to the pretreated material or hydrolysed material. Moreover, the present invention provides the use of dithionite for decreasing the fermentation inhibitory properties of a material being subjected to simultaneous enzymatic hydrolysis and fermentation.

A method for mitigating fouling in a wash unit used in a hydrocarbon cracking process wherein the fouling is due to the presence of polymers and deposits thereof formed by condensation of carbonyl compounds contained within a feed stream of the wash unit. In one embodiment, the invention provides a method of mitigating fouling in a wash unit by introducing into the feed stream an effective amount of an additive including: an inorganic salt of dithionite; and an epsilon caprolactam or a 6-amino caproic acid derivable therefrom. The additive scavenges the carbonyl compounds contained within the feed stream and dissolves deposits of the polymers to thereby mitigate fouling in the wash unit.

The present invention relates to a method for preparing dithionite solution with a reaction wherein sodium bisulfite is reduced with sodium borohydride solution to obtain dithionite, wherein the rise of the pH of the solution is prevented by adjusting the pH with carbon dioxide.

The present invention provides a method for decreasing the fermentation inhibition in a process for producing a target chemical from a pretreated cellulosic material, the process comprising enzymatic hydrolysis of the pretreated cellulosic material and fermentation of hydrolysed material, wherein the fermentation inhibitory properties of the material subjected to fermentation is decreased by an addition of at least one reducing agent to the pretreated material or hydrolysed material. Moreover, the present invention provides the use of dithionite for decreasing the fermentation inhibitory properties of a material being subjected to simultaneous enzymatic hydrolysis and fermentation.

Methods for treating lignocellulosic material or pigment with a reductive bleaching solution generally include washing the lignocellulosic material or pigment with a reducing agent of magnesium dithionite. The method includes at least one reductive stage and at least one peroxide stage. Also disclosed are methods for preparing dithionite solution wherein magnesium bisulfite is reduced with borohydride solution to obtain dithionite. Bleached lignocellulosic material or pigment obtained with the treatment methods are also disclosed.

The invention discloses a method for dyeing fabrics by using borohydride, bisulfite and thiourea dioxide (TD) as composite reducing agents. Wherein, bisulfite and borohydride are used to prepare dithionite, and its consumption is half of that when not mixed with thiourea dioxide, and the consumption of thiourea dioxide is about one-tenth of that of dithionite. Compared with the dyeing method using only dithionite as reducing agent, the method has no obvious difference in dyeing effect, but the reducing agent used is relatively safer, more stable, has higher utilization rate, and has greater economic value. At the same time, the fabric dyed by this method has good level dyeing property and washing resistance, and is an ideal dyeing method.

The invention provides a colorimetric fluorescent bifunctional molecular probe, a preparation method of the probe and an application of the probe in detection of illegal additivesodium dithionite in food samples, and belongs to the technical field of analytical chemistry. The probe has a molecular formula of C29H31N4O<+> and a structural formula represented by a formula I shown in the description.The sodium dithionite colorimetric fluorescent bifunctional molecular probe designed by the invention has a simple preparation method and a mature synthetic route, can realize direct detection of thesodium dithionite, and has the characteristics of good selectivity, a fast detection speed, high sensitivity and obvious color change; and the method provided by the invention has original innovationand good social value, and is expected to be applied to the detection of illegal additives such as the sodium dithionite in food.

The present invention concerns a tin plating bath comprising tin ions; titanium ions as reducing agent suitable to reduce tin ions to metallic tin; and at least one compound selected from the group consisting sulfites, dithionites, thiosulfates, tetrathionates, polythionates, disulfites, sulfides, disulfide, polysulfide, elemental sulfur or mixtures thereof. The present invention further discloses a method of depositing tin or a tin alloy onto a surface of a substrate. The tin plating bath is particularly suitable to be used in the electronics and semiconductor industry.

The invention relates to the technical field of vat dye dyeing, in particular to an anolyte for indirect electrochemical dyeing of vat dyes, the electrolyte of which includes sulfite, pyrosulfite, dithionite or thiocyanate at least one. The present invention adopts an electrolyte with excellent electrical conductivity and less side reactions and weak reducibility, and selects sulfite, pyrosulfite, dithionite or thiocyanate as the anode electrolyte, which has a strong ability to conduct electrons, and can be used on the anode. The reaction is fast, the product is sulfate, clean and environmentally friendly, the dyeing process under this system is simple, the reduction time is shortened, and the current efficiency is high, which is conducive to the realization of industrial production and has good application prospects. It solves the traditional anolyte such as sulfuric acid and other electrode corrosion Serious, poor safety, long recovery time, low current efficiency and other problems.

Multi-component package unit (kit-of-parts), ready-to-use agent, and methods for reductive decolorizing of dyed keratinous fibers are provided herein. In an embodiment, a multi-component package unit includes, separately packaged, a first container (A), a second container (B), and a third container (C). The first container (A) includes a cosmetic agent (a) that includes (a1) one or multiple reducing agents chosen from the group of formamidine sulfinic acid, sodium dithionite, zinc dithionite, potassium dithionite, hydroxymethanesulfinic acid, aminomethanesulfinic acid, cysteine, thiolactic acid, sulphanylacetic acid (thioglycolic acid) and / or ascorbic acid. The second container (B) includes a cosmetic agent (b) that includes one or multiple oxidizing agents. The third container (C) includes a cosmetic agent (c) that includes (c1) one or multiple alkalizing agents. The weight ratio of the total amount of all reducing agents (a1) to the total amount of all oxidants (b1) has a value from about 50.0 to about 4.0.