Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sulfur environmental

The potential advantages of LPG concern essentially the environmental aspects. LPG s are simple mixtures of 3- and 4-carbon-atom hydrocarbons with few contaminants (very low sulfur content). LPG s contain no noxious additives such as lead and their exhaust emissions have little or no toxicity because aromatics are absent. This type of fuel also benefits often enough from a lower taxation. In spite of that, the use of LPG motor fuel remains static in France, if not on a slightly downward trend. There are several reasons for this situation little interest from automobile manufacturers, reluctance on the part of automobile customers, competition in the refining industry for other uses of and fractions, (alkylation, etherification, direct addition into the gasoline pool). However, in 1993 this subject seems to have received more interest (Hublin et al., 1993). [Pg.230]

To solve some of the environmental problems of mixed-acid nitration, we were able to replaee sulfuric acid with solid superacid catalysts. This allowed us to develop a novel, clean, azeotropic nitration of aromatics with nitric acid over solid perfluorinated sulfonic acid catalysts (Nafion-H). The water formed is continuously azeotroped off by an excess of aromatics, thus preventing dilution of acid. Because the disposal of spent acids of nitration represents a serious environmental problem, the use of solid aeid eatalysts is a significant improvement. [Pg.105]

One of the things that environmental scientists do IS to keep track of important elements in the biosphere—in what form do these ele ments normally occur to what are they transformed and how are they returned to their normal state Careful studies have given clear although compli cated pictures of the nitrogen cycle the sulfur cy cle and the phosphorus cycle for example The carbon cycle begins and ends with atmospheric carbon dioxide It can be represented in an abbrevi ated form as... [Pg.66]

Nitric Phosphate. About 15% of worldwide phosphate fertilizer production is by processes that are based on solubilization of phosphate rock with nitric acid iastead of sulfuric or phosphoric acids (64). These processes, known collectively as nitric phosphate or nitrophosphate processes are important, mainly because of the iadependence from sulfur as a raw material and because of the freedom from the environmental problem of gypsum disposal that accompanies phosphoric acid-based processes. These two characteristics are expected to promote eventual iacrease ia the use of nitric phosphate processes, as sulfur resources diminish and/or environmental restrictions are tightened. [Pg.231]

Neste patented an industrial route to a cellulose carbamate pulp (90) which was stable enough to be shipped into rayon plants for dissolution as if it were xanthate. The carbamate solution could be spun into sulfuric acid or sodium carbonate solutions, to give fibers which when completely regenerated had similar properties to viscose rayon. When incompletely regenerated they were sufficientiy self-bonding for use in papermaking. The process was said to be cheaper than the viscose route and to have a lower environmental impact (91). It has not been commercialized, so no confirmation of its potential is yet available. [Pg.352]

Environmental considerations also were reflected in coal production and consumption statistics, including regional production patterns and economic sector utilization characteristics. Average coal sulfur content, as produced, declined from 2.3% in 1973 to 1.6% in 1980 and 1.3% in 1990. Coal ash content declined similarly, from 13.1% in 1973 to 11.1% in 1980 and 9.9% in 1990. These numbers clearly reflect a trend toward utilization of coal that produces less SO2 and less flyash to capture. Emissions from coal in the 1990s were 14 x 10 t /yr of SO2 and 450 x 10 t /yr of particulates generated by coal combustion at electric utiUties. The total coal combustion emissions from all sources were only slightly higher than the emissions from electric utiUty coal utilization (6). [Pg.4]

A significant issue in combustors in the mid-1990s is the performance of the process in an environmentally acceptable manner through the use of either low sulfur coal or post-combustion clean-up of the flue gases. Thus there is a marked trend to more efficient methods of coal combustion and, in fact, a combustion system that is able to accept coal without the necessity of a post-combustion treatment or without emitting objectionable amounts of sulfur oxides, nitrogen oxides, and particulates is very desirable (51,52). [Pg.72]

The complex nature of coal as a molecular entity (2,3,24,25,35,37,53) has resulted ia the chemical explanations of coal combustion being confined to the carbon ia the system. The hydrogen and other elements have received much less attention but the system is extremely complex and the heteroatoms, eg, nitrogen, oxygen, and sulfur, exert an influence on the combustion. It is this latter that influences environmental aspects. [Pg.73]

There are environmental concerns over the use of HE catalyst. The refining industry has taken steps to reduce the likelihood of an accidental release and to minimizp the environmental impact in the event of a release. As a result of these environmental concerns, most new units use sulfuric acid catalysts. [Pg.185]

Sulfur. Sulfur in diesel fuel should be kept below set limits for both environmental and operational reasons. Operationally, high levels of sulfur can lead to high levels of corrosion and engine wear owing to emissions of SO that can react with condensed water during start-up to form sulfuric acids. From an environmental perspective, sulfur bums to SO2 and SO, the exact spHt being a function of temperature and time in the combustion chamber. [Pg.192]

Partial oxidation of heavy Hquid hydrocarbons requires somewhat simpler environmental controls. The principal source of particulates is carbon, or soot, formed by the high temperature of the oxidation step. The soot is scmbbed from the raw synthesis gas and either recycled back to the gasifier, or recovered as soHd peUetized fuel. Sulfur and condensate treatment is similar in principle to that required for coal gasification, although the amounts of potential poUutants generated are usually less. [Pg.428]

After sulfuric acid work-up (accompanied by the formation of sodium sulfate), the resorcinol is extracted and isolated in a 94% yield based on y -benzenedisulfonic acid [98-48-6]. In addition to the technical complexity that goes along with the manipulation of soHds at high temperature, this process produces large amounts of salts (sulfite and sulfate salts) which economically as well as environmentally are not always desired. [Pg.487]

For environmental reasons, the entire process is handled by enclosed equipment. Lead recoveries of 96% can be obtained from the raw materials, and sulfur dioxide gas released in the process is used to produce sulfuric acid. Four plants are in operation as of 1994. Three are in Russia and one is in Italy. [Pg.38]

In the United States and increasingly in other parts of the world, environmental regulations prohibit the combustion of all but very low sulfur-content coals without sulfur oxide emission controls. The cost of installing sulfur oxide control equipment together with concern about equipment rehabihty have led to the shipment of the lower rank low sulfur coals from up to 1600 km away from the mining site. [Pg.153]

The sulfur dioxide produced by the process is usually converted to sulfuric acid, or sometimes Hquified, and the design of modem roasting faciUties takes into account the need for an efficient and environmentally clean operation of the acid plant (see SuLFURiC ACID AND SULFURTRIOXIDe). [Pg.165]

The aqueous sodium naphthenate phase is decanted from the hydrocarbon phase and treated with acid to regenerate the cmde naphthenic acids. Sulfuric acid is used almost exclusively, for economic reasons. The wet cmde naphthenic acid phase separates and is decanted from the sodium sulfate brine. The volume of sodium sulfate brine produced from dilute sodium naphthenate solutions is significant, on the order of 10 L per L of cmde naphthenic acid. The brine contains some phenolic compounds and must be treated or disposed of in an environmentally sound manner. Sodium phenolates can be selectively neutralized using carbon dioxide and recovered before the sodium naphthenate is finally acidified with mineral acid (29). Recovery of naphthenic acid from aqueous sodium naphthenate solutions using ion-exchange resins has also been reported (30). [Pg.511]

Safety provisions have proven highly effective. The nuclear power industry in the Western world, ie, outside of the former Soviet Union, has made a significant contribution of electricity generation, while surpassing the safety record of any other principal industry. In addition, the environmental record has been outstanding. Nuclear power plants produce no combustion products such as sulfuric and nitrous oxides or carbon dioxide (qv), which are... [Pg.234]

Air Pollution. Particulates and sulfur dioxide emissions from commercial oil shale operations would require proper control technology. Compliance monitoring carried out at the Unocal Parachute Creek Project for respirable particulates, oxides of nitrogen, and sulfur dioxide from 1986 to 1990 indicate a +99% reduction in sulfur emissions at the retort and shale oil upgrading faciUties. No violations for unauthorized air emissions were issued by the U.S. Environmental Protection Agency during this time (62). [Pg.355]

To overcome these difficulties, drilling fluids are treated with a variety of mud lubricants available from various suppHers. They are mostly general-purpose, low toxicity, nonfluorescent types that are blends of several anionic or nonionic surfactants and products such as glycols and glycerols, fatty acid esters, synthetic hydrocarbons, and vegetable oil derivatives. Extreme pressure lubricants containing sulfurized or sulfonated derivatives of natural fatty acid products or petroleum-base hydrocarbons can be quite toxic to marine life and are rarely used for environmental reasons. Diesel and mineral oils were once used as lubricants at levels of 3 to 10 vol % but this practice has been curtailed significantly for environmental reasons. [Pg.183]

Gas purification processes fall into three categories the removal of gaseous impurities, the removal of particulate impurities, and ultrafine cleaning. The extra expense of the last process is only justified by the nature of the subsequent operations or the need to produce a pure gas stream. Because there are many variables in gas treating, several factors must be considered (/) the types and concentrations of contaminants in the gas (2) the degree of contaminant removal desired (J) the selectivity of acid gas removal required (4) the temperature, pressure, volume, and composition of the gas to be processed (5) the carbon dioxide-to-hydrogen sulfide ratio in the gas and (6) the desirabiUty of sulfur recovery on account of process economics or environmental issues. [Pg.209]

The significance of the total sulfur content of kerosene varies greatly with the type of oil and the use to which it is put. Sulfur content is of great importance when the kerosene to be burned produces sulfur oxides, which are of environmental concern. The color of kerosene is of Htde significance but a product darker than usual may have resulted from contamination or aging in fact, a color darker than specified may be considered by some users as unsatisfactory. Kerosene, because of its use as a burning oil, must be free of aromatic and unsaturated hydrocarbons the desirable constituents of kerosene are saturated hydrocarbons. [Pg.211]


See other pages where Sulfur environmental is mentioned: [Pg.574]    [Pg.25]    [Pg.293]    [Pg.574]    [Pg.25]    [Pg.293]    [Pg.264]    [Pg.284]    [Pg.264]    [Pg.37]    [Pg.182]    [Pg.366]    [Pg.242]    [Pg.378]    [Pg.199]    [Pg.510]    [Pg.564]    [Pg.3]    [Pg.72]    [Pg.172]    [Pg.551]    [Pg.400]    [Pg.427]    [Pg.428]    [Pg.422]    [Pg.175]    [Pg.242]    [Pg.130]    [Pg.136]    [Pg.477]    [Pg.511]    [Pg.482]    [Pg.482]   
See also in sourсe #XX -- [ Pg.629 ]




SEARCH



© 2024 chempedia.info