GB723114A - Improvements in or relating to a method of producing diphenyl and homologues thereof - Google Patents

Improvements in or relating to a method of producing diphenyl and homologues thereof

Info

Publication number
GB723114A
GB723114A GB26904/51A GB2690451A GB723114A GB 723114 A GB723114 A GB 723114A GB 26904/51 A GB26904/51 A GB 26904/51A GB 2690451 A GB2690451 A GB 2690451A GB 723114 A GB723114 A GB 723114A
Authority
GB
United Kingdom
Prior art keywords
tube
per cent
conversion
time
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB26904/51A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB723114A publication Critical patent/GB723114A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/2415Tubular reactors
    • B01J19/243Tubular reactors spirally, concentrically or zigzag wound
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/76Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00132Controlling the temperature using electric heating or cooling elements
    • B01J2219/00135Electric resistance heaters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/0015Controlling the temperature by thermal insulation means
    • B01J2219/00155Controlling the temperature by thermal insulation means using insulating materials or refractories

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

<PICT:0723114/IV (b)/1> Diphenyl and its homologues are produced by passing a monocyclic aryl hydrocarbon through a tubular reactor heated substantially throughout its entire length to a temperature which is constant and lies within the limits of 773 DEG and 1073 DEG K. thereby converting from 1-30 per cent by weight of said hydrocarbon in a sojourn time of from 0.56-100 seconds. The reaction temperature and sojourn time are correlated in accordance with the equation <FORM:0723114/IV (b)/1> <FORM:0723114/IV (b)/2> where k is the reaction velocity constant, t is the sojourn time, a is the initial concentration of the hydrocarbon, x is the amount decomposing in time t, A has values of 4x108 and 1.1x109 when E has values of 45738 and 49006 cal./mol. DEG K. respectively, e is the base of the natural logarithms, R is the gas constant having the value 1.986, and K is the absolute temperature. It is also desirable to correlate the diameter of the reactor tube (d), the vapour velocity (u), the vapour density (p), and the vapour viscosity (U), so that the Reynolds' number (d.u.p/U) is from 600-100,000, particularly 3000-70,000. By recycling unreacted benzene, an overall conversion to diphenyl of about 93 per cent is obtained with 5 per cent conversion per pass or about 65 per cent with 30 per cent conversion per pass. The pressure may range from 0-100, preferably 0-40, p.s.i.g. A graph is given wherein conversion is plotted against sojourn time at different temperatures. Time and temperature having been selected, the conversion (x) is read off when the value of k can be determined from the above equation. The activation energy E is determined from the equation <FORM:0723114/IV (b)/3> and hence the values of A. Apparatus may comprise coiled preheater tube 1, heated from power lines 12, 15 connected to copper plates 11, 14, and connected to exit tube 13 from which samples of product can be collected via line 20. Tube 13 is connected to reactor tube 24 surrounded by alundum pipe 26 wrapped in nichrome heater ribbon. Tube 24 terminates in straight section 32 connected to exit pipe 33. Thermocouples 7, 29, 34, 35 are provided. Product vapours pass to condensers 42, 43, 44. Tubes 1, 24 may be of nickel steel, mild steel, iron, copper or copper-manganese alloys. Promoters such as acetone may be present during the pyrolysis. In addition to benzene, toluene, xylene, ethylbenzene, propylbenzene, and their mixtures may be pyrolyzed.
GB26904/51A 1950-11-18 1951-11-16 Improvements in or relating to a method of producing diphenyl and homologues thereof Expired GB723114A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US723114X 1950-11-18

Publications (1)

Publication Number Publication Date
GB723114A true GB723114A (en) 1955-02-02

Family

ID=22106814

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26904/51A Expired GB723114A (en) 1950-11-18 1951-11-16 Improvements in or relating to a method of producing diphenyl and homologues thereof

Country Status (1)

Country Link
GB (1) GB723114A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114149299A (en) * 2021-12-08 2022-03-08 涉县津东经贸有限责任公司 Preparation method of biphenyl

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114149299A (en) * 2021-12-08 2022-03-08 涉县津东经贸有限责任公司 Preparation method of biphenyl

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