Propane chemicals

A major use of propane recovered from natural gas is the production of light olefins by steam cracking processes. However, more chemicals can be obtained directly from propane by reaction with other reagents than from ethane. This may be attributed to the relatively higher reactivity of propane than ethane due to presence of two secondary hydrogens, which are easily substituted. 

The following reviews some of the important reactions and chemicals based on propane. 

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Bis(4-hydroxyphenylpropane 4,4 -Bis-phenol a p,p -Dihydroxydiphenylpropane 2,2-(4,4-di-hydroxydiphenyl)propane 4,4 -Dihydroxdiphe-nylpropane 4,4 -Dihydroxydiphenyl-2,2-propane 4,4 -Dihydroxy-2,2-diphenylpropane Dimethyl-methylene-/ ,p -diphenol )S-di-/7-Hydroxyphenyl-propane Dimethyl bis(/ -hydroxyphenyl)methane Diphenylolpropane 2,2-di(4-Phenylol)propane /7,p -Isopropylidenebisphenol 4,4 -Dimethyl-methylenediphenol Phenol, 4,4 -( 1-methylethyli-dene) bis- 2,2-Bis(4,4 -hydroxyphenyl)propane Chemical/Pharmaceutical/Other Class Phenolic Chemical Structure ... 

ChemicalDesignations-. Tiof nu Glycerol 1,2,3-Propanetriol l,2,3-Trihydro Q propane Chemical Formula H0CHjCH(0H)CH20H. 

Berner, U., Faber, E., Scheeder, G. Panten, D. 1995. Primary cracking of algal and landplant kerogens kinetic models of isotope variations in methane, ethane and propane. Chemical Geology, 126(3/4), 233-245. 

Under certain conditions of temperature and pressure, and in the presence of free water, hydrocarbon gases can form hydrates, which are a solid formed by the combination of water molecules and the methane, ethane, propane or butane. Hydrates look like compacted snow, and can form blockages in pipelines and other vessels. Process engineers use correlation techniques and process simulation to predict the possibility of hydrate formation, and prevent its formation by either drying the gas or adding a chemical (such as tri-ethylene glycol), or a combination of both. This is further discussed in SectionlO.1. 

Despite these simplifications, a typical or F NMR spectrum will nomially show many couplings. Figure BTl 1.9 is the NMR spectrum of propan-1-ol in a dilute solution where the exchange of OH hydrogens between molecules is slow. The underlymg frequency scale is included with the spectrum, in order to emphasize how the couplings are quantified. Conveniently, the shift order matches the chemical order of die atoms. The resonance frequencies of each of the 18 resolved peaks can be quantitatively explained by the four... 

Figure Bl.11.9. Integrated 250 MHz H NMR spectrum of dilute propan-1-ol in dinrethylsulfoxide solvent. Here, the shift order parallels the chemical order. Arr expansion of the H2-I nrultiplet is included, as is the implicit frequency scale, also referenced here to TMS = 0.

To make isosafrole or propenylbenzene the chemist will do exactly what was done for piperonal except that the chemical in three-neck flask is going to be 30g of propanal chilled to -15°C. The addition is the same except that after the solution reaches room temperature, the ice tray is removed, heat is applied and the... 

This method is merely an application of the Grignard reaction but is a lot less troublesome because it uses really common chemicals. This method can be done as it was done in the reference where a phenylbutene was made using a bromopropane ( bromo-propane and bromoethane are cheap to purchase or can be made... 

The decreased shielding caused by electronegative substituents is primarily an inductive effect and like other inductive effects falls off rapidly as the number of bonds between the substituent and the proton increases Compare the chemical shifts of the pro tons m propane and 1 mtropropane... 

Protons are equivalent to one another and have the same chemical shift when they are m equivalent environments Often it is an easy matter to decide simply by mspec tion when protons are equivalent or not In more difficult cases mentally replacing a proton m a molecule by a test group can help We 11 illustrate the procedure for a sim pie case—the protons of propane To see if they have the same chemical shift replace one of the methyl protons at C 1 by chlorine then do the same thing for a proton at C 3 Both replacements give the same molecule 1 chloropropane Therefore the methyl protons at C 1 are equivalent to those at C 3... 

SPEC benchmark Special-duty propane Special effects Specialty chemicals... 

Natural gas Hquids represent a significant source of feedstocks for the production of important chemical building blocks that form the basis for many commercial and iadustrial products. Ethyleae (qv) is produced by steam-crackiag the ethane and propane fractions obtained from natural gas, and the butane fraction can be catalyticaHy dehydrogenated to yield 1,3-butadiene, a compound used ia the preparatioa of many polymers (see Butadiene). The / -butane fractioa can also be used as a feedstock ia the manufacture of MTBE. 

Commercial VPO of propane—butane mixtures was in operation at Celanese Chemical Co. plants in Texas and/or Canada from the 1940s to the 1970s. The principal primary products were acetaldehyde, formaldehyde, methanol, and acetone. The process was mn at low hydrocarbon conversion (3—10%) and a pressure in excess of 790 kPa (7.8 atm). These operations were discontinued because of various economic factors, mainly the energy-intensive purification system required to separate the complex product streams. 

The main commercial source of methane, ethane, and propane is natural gas, which is found ia many areas of the world ia porous reservoirs they are associated either with cmde oil (associated gas) or ia gas reservoirs ia which no oil is present (nonassociated gas). These gases are basic raw materials for the organic chemical industry as well as sources of energy. The composition of natural gas varies widely but the principal hydrocarbon usually is methane (see Gas, natural). Compositions of typical natural gases are Hsted ia Table 2. 

Relatively small amounts of methane, ethane, and propane also are produced as by-products from petroleum processes, but these usually are consumed as process or chemical feedstock fuel within the refineries. Some propane is recovered and marketed as LPG. 

About 35% of total U.S. LPG consumption is as chemical feedstock for petrochemicals and polymer iatermediates. The manufacture of polyethylene, polypropylene, and poly(vinyl chloride) requires huge volumes of ethylene (qv) and propylene which, ia the United States, are produced by thermal cracking/dehydrogenation of propane, butane, and ethane (see Olefin polymers Vinyl polymers). 

The most important commercial chemical reactions of phenol are condensation reactions. The condensation reaction between phenol and formaldehyde yields phenoHc resins whereas the condensation of phenol and acetone yields bisphenol A (2,2-bis-(4-hydroxyphenol)propane). PhenoHc resins and bisphenol A [80-05-7] account for more than two-thirds of U.S. phenol consumption (1). 

Of the many forms of carbon and graphite produced commercially, only pyrolytic graphite (8,9) is produced from the gas phase via the pyrolysis of hydrocarbons. The process for making pyrolytic graphite is referred to as the chemical vapor deposition (CVD) process. Deposition occurs on some suitable substrate, usually graphite, that is heated at high temperatures, usually in excess of 1000°C, in the presence of a hydrocarbon, eg, methane, propane, acetjiene, or benzene. 

Glutaraldehyde (1,3-diformyl propane) is a powerful, cold disinfectant. It is used principally in aqueous solution as a biocide and chemical disinfectant. It has been widely used in the health services, e.g. in operating theatres, endoscopy units, dental units and X-ray film processing. 

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