The setup as instructed by my supervisor consisted of a simple watercooled liebig condenser. Dcpd products from dow can best be characterized as highly reactive intermediates used for a wide range of resins, i. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed. Thermal cracking is a process in which hydrocarbons present in crude oil are subject to high heat and temperature to break the molecular bonds and breaking down longchained, higher boiling hydrocarbons into shorterchained, lower boiling hydrocarbons. Suitable heat transfer fluids include molten diphenylether, molten diphenylmethane, molten decalin, molten tetralin, and dowtherm. Thermal properties of ruthenium alkylidenepolymerized. Sep 14, 2001 the dimerization is highly exothermic.
The accompanying compounds have similar molecular weight and boiling points as dicyclopentadiene. Liquidphase cracking of dicyclopentadiene by reactive. It is usually in the form of polymer because its monomer is easy to polymerize at room temperature. Thermal cracking of dielsalder adducts equistar chemicals, lp. In the thermal cracking process, the compound to be cracked is subjected to high heat and pressure. This thermal cracking dimerization method does not give directly a dcpd of purity suitable for metathesis polymerization. Dicyclopentadiene, abbreviated dcpd, is a chemical compound with formula c 10 h 12. The apparatus for the cracking of dicyclopentadiene to cyclopentadiene will be set up. C can be obtained addition of iron powder expedites the thermal decomposition rate of cyclopentadiene. Cyclopentadiene cpd, boiling at 42c, is an unsaturated, high. No studies on gas phase thermal cracking of dcpd to produce cpd and. Monomer and dimer are close enough in boiling point that a sloppy job will deliver a lot of dimer to the collection pot, which is a real pain to remove from many dielsalder product mixtures. The dcpd must be fractionally distilled to remove the aforementioned low boiling c.
Because of its reactivity, cyclopentadiene is normally available only in the stable dimer form. Factors including cracking temperature, reaction time, and h 2 to dcpd ratios were studied. The process of producing highpurity cyclopentadiene cpd has been investigated, including a gas phase thermal cracking process of dicyclopentadiene dcpd in the presence of h 2 on a continuous bed reactor and batch distillation for the further separation. I recently did a distillation of dicyclopentadiene bp 166 c to get cyclopentadiene bp 40 c. This substance is essentially insoluble in water and soluble in alcohol, acetic acid and ether. And 180 dc is a bit much, id just stay under the boiling point of the dimer. Highpurity dcpd in the range of 9899% is produced by thermal cracking of the lowerpurity dcpd. Vaporphase thermal cracking of dcpd is usually used as a step of process for manufacturing high purity dcpd.
A reactive distillation process was developed for cracking dicyclopentadiene dcpd to produce cyclopentadiene cpd. Liquidphase cracking of dicyclopentadiene by reactive distillation. Dicyclopentadiene may react vigorously with oxidizing agents. The separation of the lowboiling c5 components from the dcpd is achieved by. Thermal degradation kinetics and flame retardancy of. Jan 25, 2012 what kind of reaction does the cracking of dicyclopentadiene represent. View lab report lab report 1 from che 211l at quinnipiac university. Oct 22, 2001 cyclopentadiene cpd and dicyclopentadiene dcpd, which occur as by.
Gas phase cracking of dicyclopentadiene to produce. Can undergo exothermic polymierization reactions in the presence of various catalysts such as acids or initiators, if subjected to heat for prolonged periods, or if contaminated. Production of polymerization grade dicyclopentadiene. Paraffin oil has a boiling point greater than 370 c. At room temperature, it is a clear light yellow color liquid with an acrid odor. Dicyclopentadiene is coproduced in large quantities in the steam cracking of naphtha and gas oils to ethylene. Dicyclopentadiene, abbreviated dcpd, is a chemical compound with formula c 10h12. Cracking of dicyclopentadiene was my simple liebig condenser.
The accompanying compounds have similar molecular weight and boiling points as dicyclopentadiene, so that. Qilong mcpd is rectified from c9 fraction, a byproduct of naphtha cracking. What was the purpose of adding paraffin to the reaction flask when cracking dicyclopentadiene. The osha analytical laboratory recently received a set of field samples that required analysis for dicyclopentadiene. To aid in product isolation, the entire reaction will. Hithertofore, when coducting thermal cracking of dcpd, coke formation within cracking tubes is the most serious and troublesome problem. Cyclopentadiene is made by thermal cracking of its dimer, and on standing it slowly reverts to this species. Phase thermal cracking of dicyclopentadiene is in the cyclopentadiene according to the invention can be used as primary source material dcpd from cracking oil, clean or with the content of thi about 10 wt. Dicyclopentadiene is coproduced in large quantities in the steam cracking of. Cyclopentadiene and dicyclopentadiene cheung major. Mar 02, 2009 dicyclopentadiene 195g is placed in the two necked flask and heated to about 160.
Cyclopentadiene cpd and dicyclopentadiene dcpd, which occur as byproducts in the steam cracking process in ethylene plants, are the major ingredients in the production of hydrocarbon resins. Experiment 14 the dielsalder cycloaddition reaction pg. Pure cpd can be produced in situ by the thermal cracking of the dcpd at a temperature near the normal boiling point of the dcpd. Give the structure of the product for each dielsalder reaction shown below. You cannot distill cp which has not formed by thermal cracking of the dicyclopentadiene which is slow. Long dimerizer residence times at elevated temperatures i. The impact of storage conditions on thermal stability.
More preferably, the liquid coolant is diphenyl ether, having a boiling point of 258260c. The c9c10 fraction formally contains all kinds of diels alder adducts because the various c5 diolefin molecules form dimers during the process steps of the ethylene manufacturing process. It is soluble in ethyl ether, ethyl alcohol and benzene while insoluble in water. A process and a system for cracking dicyclopentadiene are disclosed pursuant to the process preheated dicyclopentadiene is introduced into a heated transfer fluid sufficiently below the transfer fluid surface to accomplish substantially complete conversion of said dicyclopentadiene to monomeric cyclopentadiene vapor. The friedrichs condenser is for refluxing dicyclopentadiene bp 170 c. Dcpd is a common byproduct in the naphtha cracking process 19. Due to the inconvenience of sampling with an impinger, we set out to find a solid sorbent tube to collect the dicyclopentadiene. In the autoclave reactor, reaction temperature, reaction time, diluent, and inhibitors are investigated to study the effect of inhibiting oligomerization reactions. Dielsalder reaction of cyclopentadiene with maleic anhydride johnson, chad philip.
Dcpd products originate from high temperature cracking of petroleum fractions and are best characterized as highly reactive intermediates used for a. Hithertofore, when conducting thermal cracking of dcpd, coke formation within cracking tubes is the most serious and troublesome problem. The dicyclopentadiene and the impurities are returned to the cracking zone or. Any inert heat transfer fluid boiling above the cracking temperature of dicyclopentadiene may be utilized.
Oct 31, 2016 a process and a system for cracking dicyclopentadiene are disclosed pursuant to the process preheated dicyclopentadiene is. The air samples had been collected with isopropyl alcohol impingers. Perfect methyl cyclopentadiene dimer provided by hydrocarbon. The largest consumption of dicyclopentadiene is linked to the production of resins including unsaturated polyester resins, petroleum resins, terpolymers, polynorbornenes, and other cyclic olefin polymers. Thermal gravimetric analyses tga were performed on a perkinelmer tga7 thermal analyzer 710 mg samples using various heating rates of 5, 10, 20 and 40 cmin in n 2 at a purge pressure of 25 psi within the temperature range of 30800 c. Preparation of cyclopentadiene from dicyclopentadiene. Dicyclopentadiene should never be distilled to dryness since there is danger of explosion if peroxides are present.
May react exothermically with reducing agents to release hydrogen gas. Preparation of cyclopentadiene from its dimer journal of. May 09, 2006 this invention relates to thermal cracking of dielsalder adducts to form a thermally cracked cracked product that contains at least the original compounds from which the adducts were formed, and recovering at least one of the thus formed original compounds from the cracked product. Cyclopentadiene and dicyclopentadiene researchgate. Expired lifetime application number us836500a inventor leland k beach. Us patent for process for the vaporphase thermal cracking of. Dielsalder reaction of cyclopentadiene with maleic anhydride. Modern highpressure thermal cracking operates at absolute pressures of about 7,000 kpa. Also, when cooling a piece of equipment that contains the hot bottoms from the distillation or cracking of dicyclopentadiene, care should be taken to exclude air.
The dicyclopentadiene is added at a rate sufficient to maintain a continuous. In many teaching and research laboratories, cyclopentadiene is prepared at frequent intervals by cracking dicyclopenta diene either neat1 or by adding it to a highboiling oil. This invention relates to the thermal decomposition of. Dicyclopentadiene is coproduced with ethylene from the c5 fraction in the steam cracking of naphtha and gas oils.
I remember adding some iron powder was supposed to speed up the retrodielsalder reaction, i guess by lowering the effective concentration of the monomer through complexion. Cracking apparatus the dielsalder reaction of cyclopentadiene with maleic anhydride the dielsalder reaction that you will be performing between cyclopentadiene and maleic anhydride occurs rapidly at room temperature. An overall process of disproportionation can be observed, where light, hydrogenrich products are formed at the expense of heavier molecules which condense and are depleted of hydrogen. Dicyclopentadiene is a colorless, flammable liquid with a boiling point of i70 c 338f. It will dissolve in water and evaporates quickly from water and soil surfaces. Paraffin oil has a boiling point greater than 370 degrees celcius. Highpurity dcpd in the range of 9899% is produced by thermal cracking of. To conduct rim, it is necessary to use high purity dicyclopentadiene dcpd as the raw material. Pure cpd cyclopentadiene is separated from the crude dcpd by distillation and is redimerized in controlled conditions to avoid oligomer formation. At its simplest, this dimerisation can be described as a. Dicyclopentadiene dcpd 3a,4,7,7atetrahydo4,7methano1hindene c10h12 general dicyclopentadiene or dcpd is the dimer of cyclopentadiene cpd formed by a dielsalder addition reaction. By rapidly removing the evolved cyclopentadiene from the heating zone this. Jun 14, 1994 an inexpensive manufacture of high purity dicyclopentadiene suitable for use as a raw material of rim is possible in an industrial scale by the use of the process for the vaporphase thermal cracking of dicyclopentadiene mentioned in preceding sentence.
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