Abstract: A system is described that includes a computing device having one or more processors and a memory. The computing device is configured to receive a first stream of first data. The computing device is further configured to perform an analysis on the first stream of first data at a first time and at a second time that is different from the first time and determine whether there is a change in the first stream of first data between the first time and the second time. In addition, the computing device is configured to, if there is a change in the first stream of first data between the first time and the second time, adjust at least one tuning parameter of an audio tuning algorithm of an audio processing system. The audio processing system is configured to process audio input using the audio tuning algorithm to generate audio output.

Abstract: A process can be used for preparing sodium and potassium alkoxides. The process is characterized by two simultaneously implemented but spatially separated reactions of an alcohol ROH with NaOH, and ROH with KOH, to give sodium alkoxide and potassium alkoxide, respectively. The vapours formed in this case contain the alcohol used and water. The vapours are combined, and the resulting mixed vapour is fed to a common distillation with recovery of the alcohol.

Abstract: A method can be used for producing alkali metal alcoholates in counter flow by reactive rectification. The alkali metal is selected from sodium and potassium. In a first part of the method, the alcohol is converted in counter flow with the respective alkali metal hydroxide. In a second part of the method, the mixture of alcohol and water obtained is separated in a rectification column, and the alcoholic vapour arising is condensed, as a result of which the temperature thereof increases. The energy dissipated during cooling of the condensed vapour is then used in the first part of the method. This permits an energy-efficient production of the alkali metal alcoholates concerned.

Abstract: A method can be used for producing alkali metal alcoholates in counter flow by reactive rectification. The alkali metal is selected from sodium and potassium. In a first part of the method, the alcohol is converted in counter flow with the respective alkali metal hydroxide. In a second part of the method, the mixture of alcohol and water obtained is separated in a rectification column, and the alcoholic vapour arising is condensed, as a result of which the temperature thereof increases. The energy dissipated during cooling of the condensed vapour is then used in the first part of the method. This permits an energy-efficient production of the alkali metal alcoholates concerned.

Abstract: A process can be used for preparing sodium and potassium alkoxides. The process is characterized by two simultaneously implemented but spatially separated reactions of an alcohol ROH with NaOH, and ROH with KOH, to give sodium alkoxide and potassium alkoxide, respectively. The vapours formed in this case contain the alcohol used and water. The vapours are combined, and the resulting mixed vapour is fed to a common distillation with recovery of the alcohol.

Abstract: An improved method is used for preparing triacetone amine while recycling the by-products. This involves treating the crude product from triacetone amine preparation, which leads to an increase in the content of compounds which react readily with ammonia. This method enables efficient recycling of the by-products formed in the synthesis of triacetone amine.

Abstract: An improved method is used for preparing triacetone amine while recycling the by-products. This involves treating the crude product from triacetone amine preparation, which leads to an increase in the content of compounds which react readily with ammonia. This method enables efficient recycling of the by-products formed in the synthesis of triacetone amine.

Abstract: An N-methyl-substituted triacetonamine compound can be produced by reacting at least one triacetonamine compound with formaldehyde under reductive conditions.

Abstract: An N-substituted triacetonediamine compound is prepared by reacting 4-amino-2,2,6,6-tetramethylpiperidine or a derivative thereof with a carbonyl compound in a reductive amination, wherein reductive conditions are established by conducting the reaction in the presence of hydrogen and in the presence of a supported catalyst, wherein the supported catalyst includes at least one metal M, wherein the metal M is selected from the group consisting of V, Cr, Mo, Mn, Ni, Pd, Pt, Fe, Ru, Os, Co, Rh, Ir, and Cu.

Abstract: A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Abstract: An N-methyl-substituted triacetonamine compound can be produced by reacting at least one triacetonamine compound with formaldehyde under reductive conditions.

Abstract: A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Abstract: In a method of absorbing CO2 from a gas mixture the use of an absorption medium comprising water and at least one amine of formula (I) where R1 is a —(CH2)n—(XCH2CH2)m—Y—R3 radical where R3=hydrogen or an alkyl radical having from 1 to 6 carbon atoms, X and Y are each, independently of one another, NR3, oxygen, SO or SO2, where in the case of Y?SO and in the case of Y?SO2, R3 is not hydrogen, and Y—R3 can be an N-morpholinyl radical or an N-piperazyl radical, n=2 to 4, m=0 to 4 and R2 is hydrogen, an alkyl radical having from 1 to 6 carbon atoms or a radical R1, where m is not 0 when R2 is not a radical R1, Y?NR3 and Y—R3 is not an N-morpholinyl radical and not an N-piperazyl radical, makes it possible to avoid precipitation of a solid during the absorption of CO2 and a separation into two liquid phases during the regeneration of the absorption medium.

Abstract: An N-methyl-substituted triacetonamine compound is prepared by reacting at least one triacetonamine compound (I) with formaldehyde under reductive conditions, in the presence of hydrogen and in the presence of a supported catalyst, wherein the supported catalyst contains at least one metal M, wherein the metal M is selected from the group consisting of V, Cr, Mo, Mn, Ni, Pd, Pt, Fe, Ru, Os, Co, Rh, Ir, and Cu.

Abstract: A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Abstract: An ECG device designed as a portable hand-held device, comprising a housing, on the outer face of which a plurality of ECG sensors in the form of capacitive electrodes is arranged in a sensor region, characterized by the following features: the EGG device has at least one flexible retaining mat in the sensor region, which retaining mat is designed to retain at least some or all ECG sensors, the retaining mat is made of liquid-tight material, at least some or all ECG sensors are fastened to the outer face of the retaining mat facing away from the housing.

Abstract: A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Abstract: A process for inhibiting the polymerization of cyclopentadiene compounds (B) by contacting the cyclopentadiene compound with a quinone methide compound (A) of structure (I), Compositions (AB) comprising (A) and (B) are also provided.

Abstract: An N-methyl-substituted triacetonamine compound is prepared by reacting at least one triacetonamine compound (I) with formaldehyde under reductive conditions, in the presence of hydrogen and in the presence of a supported catalyst, wherein the supported catalyst contains at least one metal M, wherein the metal M is selected from the group consisting of V, Cr, Mo, Mn, Ni, Pd, Pt, Fe, Ru, Os, Co, Rh, Ir, and Cu.

Abstract: An N-substituted triacetonediamine compound is prepared by reacting 4-amino-2,2,6,6-tetramethylpiperidine or a derivative thereof with a carbonyl compound in a reductive amination, wherein reductive conditions are established by conducting the reaction in the presence of hydrogen and in the presence of a supported catalyst, wherein the supported catalyst includes at least one metal M, wherein the metal M is selected from the group consisting of V, Cr, Mo, Mn, Ni, Pd, Pt, Fe, Ru, Os, Co, Rh, Ir, and Cu.