GB628403A - Improvements in or relating to the purification of naphthalene - Google Patents

Improvements in or relating to the purification of naphthalene

Info

Publication number
GB628403A
GB628403A GB3604346A GB3604346A GB628403A GB 628403 A GB628403 A GB 628403A GB 3604346 A GB3604346 A GB 3604346A GB 3604346 A GB3604346 A GB 3604346A GB 628403 A GB628403 A GB 628403A
Authority
GB
United Kingdom
Prior art keywords
naphthalene
alcohol
impurities
treated
cold
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
GB3604346A
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.)
ERIC HEREWARD JOSCELYNE
Midland Tar Distillers Ltd
Original Assignee
ERIC HEREWARD JOSCELYNE
Midland Tar Distillers Ltd
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 ERIC HEREWARD JOSCELYNE, Midland Tar Distillers Ltd filed Critical ERIC HEREWARD JOSCELYNE
Priority to GB3604346A priority Critical patent/GB628403A/en
Publication of GB628403A publication Critical patent/GB628403A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D9/00Crystallisation
    • B01D9/0004Crystallisation cooling by heat exchange
    • B01D9/0009Crystallisation cooling by heat exchange by direct heat exchange with added cooling fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/14Purification; Separation; Use of additives by crystallisation; Purification or separation of the crystals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Naphthalene containing oily impurities is crystallized and purified on introducing in the molten or vapour state into a cold or cool aliphatic alcohol having not more than four carbon atoms or a mixture of such alcohols, the alcohol being substantially anhydrous, maintained cold or cool if necessary, and present in an amount such that the greater part of the naphthalene crystallizes substantially instantaneously on contact with the alcohol while the impurities are dissolved together with only a small amount of impure naphthalene. The resultant crystals of naphthalene are preferably maintained in motion in the alcohol so as to wash them and prevent the occlusion of impurities in crystal aggregates. Methyl alcohol is the preferred alcohol and when it is used a temperature within the range of 20 DEG to 45 DEG C. is preferred. An anhydrous alcohol is stated to be one with less than 1 per cent of water. Crude naphthalene should have a naphthalene content of at least 25 per cent, preferably 55 per cent, and molten naphthalene derived from a fractional distillation of coal tar may be treated. The process may be made continuous by recycling the alcohol until it is nearly saturated with impurities, or by withdrawing a portion of impure alcohol and adding fresh alcohol for make-up purposes. In an illustration 100 parts by weight of crude naphthalene derived from vertical retort tar and with a boiling range of 211 DEG to 220 DEG C. is fed at 100 DEG C. into 140 parts by weight of cold anhydrous methyl alcohol, the crystals formed being agitated and air-dried after collection. The methyl alcohol is recycled and maintained at 35 DEG C. at the point of naphthalene entry. In a further illustration a similar naphthalene fraction is treated as above after initial refrigeration. According to the Provisional Specification solid naphthalene may also be treated.
GB3604346A 1946-12-05 1946-12-05 Improvements in or relating to the purification of naphthalene Expired GB628403A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3604346A GB628403A (en) 1946-12-05 1946-12-05 Improvements in or relating to the purification of naphthalene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3604346A GB628403A (en) 1946-12-05 1946-12-05 Improvements in or relating to the purification of naphthalene

Publications (1)

Publication Number Publication Date
GB628403A true GB628403A (en) 1949-08-29

Family

ID=10384313

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3604346A Expired GB628403A (en) 1946-12-05 1946-12-05 Improvements in or relating to the purification of naphthalene

Country Status (1)

Country Link
GB (1) GB628403A (en)

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