Patent classifications
B01D3/34
Effective novel non-polymeric and non-fouling additive for inhibiting high-temperature naphthenic acid corrosion and method of using the same
The present invention relates to inhibition of high temperature naphthenic acid corrosion occurring in hydrocarbon processing units. The invention provides an effective novel non-polymeric and non-fouling additive for inhibiting high-temperature naphthenic acid corrosion, comprising an effective corrosion-inhibiting amount of a second phosphate ester wherein said second phosphate ester is obtained by reacting a first phosphate ester with an oxirane compound selected from the group consisting of butylene oxide, ethylene oxide, propylene oxide or any other oxirane compound or a combination thereof, preferably with butylene oxide, capably yielding said second phosphate ester, having a structure A or B, ##STR00001##
wherein R.sup.1 and R.sup.2 are each independently selected from the group consisting of moieties having 1 to 20 carbon atoms and R.sup.1 and R.sup.2 may be identical or different, X is H, CH.sub.3 or C.sub.2H.sub.5; and n may vary from 1 to 20,
wherein said first phosphate ester is having a structure I or II, ##STR00002##
wherein R.sup.1 and R.sup.2 are each independently selected from the group consisting of moieties having 1 to 20 carbon atoms and R.sup.1 and R.sup.2 may be identical or different, said first phosphate ester being obtained as a reaction product of reaction of an alcohol with a phosphorous pentaoxide.
Hydrocarbon vapor recovery system with oxygen reduction
A system for reducing dioxygen (O.sub.2) present in vapors from oil storage tanks. The system may include an inlet that receives vapors from the tanks; a heating device coupled with the inlet that heats vapors to a first temperature to form heated vapor; and a vessel coupled receiving heated vapor and containing at least one catalyst to reduce dioxygen from the heated vapor. The catalyst may include palladium, and the vessel may include zinc oxide to remove sulfur from the heated vapor. A compressor may be used to compress the vapors. A controller may be provided to monitor O.sub.2 concentration in heated vapor, and the controller directs flow of heated vapor to a gas pipeline if the O.sub.2 concentration is below a predetermined level; or if the O.sub.2 concentration is unacceptably high, the controller directs flow of vapor to be re-circulated within the system to further reduce O.sub.2 concentration therein.
METHOD FOR PURIFYING HALOGENATED OLIGOSILANES
1. The present invention relates to a method for the purification of halogenated oligosilanes as a pure compound or mixture of compounds each having at least one direct Si—Si bond, the substituents thereof being exclusively halogen or halogen and hydrogen, and the composition thereof being an atom ratio of substituent:silicon of at least 3:2, by the action of at least one purification agent on the halogenated oligosilane and isolation of the halogenated oligosilane with improved purity.
2.1. In the prior art, halogenated monosilanes such as HSiCl.sub.3 are purified by treatment with preferably polymeric organic compounds containing amino groups, and are separated out from these mixtures. This method cannot be used for halogenated oligosilanes because of the contained amino groups, since secondary reactions would lead to decomposition of the products. The new method should provide the desired products in high yield and purity without amino groups being used.
2.2. The purification of the halogenated oligosilanes is carried out in the presence of special purification agents, which convert contaminations such as, for example, FeCl.sub.2 into an insoluble and/or less volatile form. A separation of the products of completes the purification This method gives a high yield and avoids the problems associated with the prior art, such as, for example, long distillation times.
2.3. The method is suitable for the purification of, for example, Si.sub.2Cl.sub.6, Si.sub.3Cl.sub.8, Si.sub.4Cl.sub.10, and higher homologs. These find application, for example, in the deposition of silicon nitride layers in CVD processes.
METHOD FOR PURIFYING HALOGENATED OLIGOSILANES
1. The present invention relates to a method for the purification of halogenated oligosilanes as a pure compound or mixture of compounds each having at least one direct Si—Si bond, the substituents thereof being exclusively halogen or halogen and hydrogen, and the composition thereof being an atom ratio of substituent:silicon of at least 3:2, by the action of at least one purification agent on the halogenated oligosilane and isolation of the halogenated oligosilane with improved purity.
2.1. In the prior art, halogenated monosilanes such as HSiCl.sub.3 are purified by treatment with preferably polymeric organic compounds containing amino groups, and are separated out from these mixtures. This method cannot be used for halogenated oligosilanes because of the contained amino groups, since secondary reactions would lead to decomposition of the products. The new method should provide the desired products in high yield and purity without amino groups being used.
2.2. The purification of the halogenated oligosilanes is carried out in the presence of special purification agents, which convert contaminations such as, for example, FeCl.sub.2 into an insoluble and/or less volatile form. A separation of the products of completes the purification This method gives a high yield and avoids the problems associated with the prior art, such as, for example, long distillation times.
2.3. The method is suitable for the purification of, for example, Si.sub.2Cl.sub.6, Si.sub.3Cl.sub.8, Si.sub.4Cl.sub.10, and higher homologs. These find application, for example, in the deposition of silicon nitride layers in CVD processes.
Selective dehydrohalogenation of tertiary halogenated hydrocarbons and removal of tertiary halogenated hydrocarbon impurities from a halogenated hydrocarbon product
A process for converting tertiary halogenated hydrocarbons in a tertiary halogenated hydrocarbon-containing stream to a corresponding unhalogenated or less-halogenated unsaturated hydrocarbon product with the release of hydrogen halide involves contacting the tertiary halogenated hydrocarbon with a sorbent-type dehydrohalogenation catalyst in a reaction zone and optionally passing a stripping gas through the reaction zone to remove vapor phase reaction products from the reaction zone. A process for removing a tertiary chlorinated hydrocarbon impurity from 1,3-dichloro-1-propene involves contacting a mixture containing the 1,3-dichloro-1-propene and the tertiary chlorinated hydrocarbon impurity with a dehydrochlorination catalyst effective to catalyze a conversion of the tertiary chlorinated hydrocarbon impurity to a corresponding unchlorinated or less-chlorinated unsaturated hydrocarbon and hydrogen chloride and distilling the 1,3-dichloro-1-propene to produce a purified cis-1,3-dichloro-1-propene fraction and a purified trans-1,3-dichloro-1-propene fraction.
Selective dehydrohalogenation of tertiary halogenated hydrocarbons and removal of tertiary halogenated hydrocarbon impurities from a halogenated hydrocarbon product
A process for converting tertiary halogenated hydrocarbons in a tertiary halogenated hydrocarbon-containing stream to a corresponding unhalogenated or less-halogenated unsaturated hydrocarbon product with the release of hydrogen halide involves contacting the tertiary halogenated hydrocarbon with a sorbent-type dehydrohalogenation catalyst in a reaction zone and optionally passing a stripping gas through the reaction zone to remove vapor phase reaction products from the reaction zone. A process for removing a tertiary chlorinated hydrocarbon impurity from 1,3-dichloro-1-propene involves contacting a mixture containing the 1,3-dichloro-1-propene and the tertiary chlorinated hydrocarbon impurity with a dehydrochlorination catalyst effective to catalyze a conversion of the tertiary chlorinated hydrocarbon impurity to a corresponding unchlorinated or less-chlorinated unsaturated hydrocarbon and hydrogen chloride and distilling the 1,3-dichloro-1-propene to produce a purified cis-1,3-dichloro-1-propene fraction and a purified trans-1,3-dichloro-1-propene fraction.
Multi-stage bubble column humidifier apparatus
A downcomer apparatus for use in a multi-stage bubble column humidifier. The humidifier comprises at least a first, second and third stage, wherein each of said stages includes an inlet, an outlet and a chamber defined by said stage, in fluid communication with the inlet and the outlet. In the humidifier, a heated liquid fluid stream flowing downwardly exchanges mass and heat with a cooler carrier gas stream flowing upwardly through the bubble column. A bubble generator comprising a perforated plate, or sparger, passes the carrier gas, such as air, from a lower chamber to form bubbles in a fluid, such as water, forming a bath on an upper chamber. An off-set arrangement of downcomer apparatuses, wherein said apparatus comprises a funnel, a watergate, and a downcomer, is used to prevent a recirculation of humid bubbles from the upper chamber to the lower chamber, thus preventing the air stream from circumventing the bubble generator in the form of the humid bubbles. This arrangement assures the maximum possible performance of the humidifier, as the entire air stream is forced to move through the bubble column, thus maximizing the air-water surface interface for an efficient mass and heat exchange.
Method and apparatus for extracting contaminants from soil and from animal manure
An apparatus for extracting contaminants from a contaminated material, such as contaminated soil and animal manure, includes an extraction tank having an interior, a heating element that is adapted heat the contaminated material to a temperature where contaminants in the contaminated material are released therefrom to the interior of the extraction tank, and an agitator that is adapted to agitate the contaminated material as it is being heated by the heating element. The apparatus also includes an air pump that generates a series of positive pressure air pulses at an outlet thereof and a series of negative pressure air pulses at the inlet thereof. The apparatus further includes one or more contaminant retaining mechanisms, such as a sediment holding tank, a fluid holding tank, and a gas filter. The interior of the extraction tank, the air pump, and the contaminant retaining mechanisms are connected in a closed loop air circulation system such that the contaminants that are released from the contaminated material are stored in the contaminant retaining mechanisms.
SYSTEM AND METHOD FOR REMOVAL OF WATER FROM OIL
The present invention relates to a system for removing water from oil from an oil supply, where the system comprises a housing comprising an inner opening, an oil inlet tube connecting the oil supply and an oil inlet of the housing, where the oil inlet tube comprises an inlet pump adapted to provide a flow of oil in a direction from said oil supply to said oil inlet, an oil outlet tube connecting an oil outlet of the housing and the oil supply, where the oil outlet tube comprises an outlet pump adapted to provide a flow of oil in a direction from said oil outlet to said oil supply, an air inlet tube providing a gas connection between an air supply unit and an air inlet of the housing, and an air outlet tube providing a gas connection between an air outlet of the housing and the air supply unit, where said outlet pump is adapted as to provide a flow at a higher pumping flow rate than the pumping flow rate provided by said inlet pump. The invention further relates to a method of removing water from oil from an oil supply.
System and method to remove organic acid from a rich MEG stream by stripping
A system and method for removing acetic acid and other short chain fatty acids described as organic acid from a rich mono-ethylene glycol (“MEG”) solution does so by stripping the organic acid from the rich MEG solution by contacting the solution with a gas, the gas being nitrogen or a fuel gas such as methane; and stripping the organic acid from the gas by contacting the gas with a caustic solution such as a dilute sodium hydroxide solution. The stripping takes place in respective stripping columns. A portion of the gas exiting the gas/organic acid stripping column can be recycled to the MEG/organic acid stripping column to reduce total gas usage. A portion of the waste stream exiting the gas/organic acid stripping column can be recycled back to the gas/organic acid stripping column to reduce the amount of caustic solution used as well as the amount of waste.