WO1991010478A1 - Waste treatment - Google Patents

Waste treatment Download PDF

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Publication number
WO1991010478A1
WO1991010478A1 PCT/GB1991/000010 GB9100010W WO9110478A1 WO 1991010478 A1 WO1991010478 A1 WO 1991010478A1 GB 9100010 W GB9100010 W GB 9100010W WO 9110478 A1 WO9110478 A1 WO 9110478A1
Authority
WO
WIPO (PCT)
Prior art keywords
acid
give
ketone
alcohol
solid
Prior art date
Application number
PCT/GB1991/000010
Other languages
French (fr)
Inventor
Alan Lionel Hudd
Naser Reza
Original Assignee
Domino Printing Sciences Plc
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 Domino Printing Sciences Plc filed Critical Domino Printing Sciences Plc
Publication of WO1991010478A1 publication Critical patent/WO1991010478A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D3/00Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
    • A62D3/30Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/72Organic compounds not provided for in groups B01D53/48 - B01D53/70, e.g. hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805Compounds having only one group containing active hydrogen
    • C08G18/2815Monohydroxy compounds
    • C08G18/282Alkanols, cycloalkanols or arylalkanols including terpenealcohols
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D2101/00Harmful chemical substances made harmless, or less harmful, by effecting chemical change
    • A62D2101/20Organic substances
    • A62D2101/28Organic substances containing oxygen, sulfur, selenium or tellurium, i.e. chalcogen

Definitions

  • This invention relates to the treatment of waste liquid or vapour containing volatile solvents, especially spent inks.
  • Inks e.g. those used in ink-jet printing, comprise a mixture of inflammable solvents, primarily methyl ethyl ketone (MEK) and alcohols such as ethanol, propanol and/or butanol.
  • MEK methyl ethyl ketone
  • alcohols such as ethanol, propanol and/or butanol.
  • waste liquid or vapour containing an alcohol and/or a ketone is treated in a manner which converts the hazardous component to a harmless, non-inflammable solid which can be disposed of simply and safely.
  • the reactant for the alcohol is a monomer-free isocyanate, which can give a solid polyurethane.
  • the reactant for the ketone is a urea, acid, ammonium compound or bisulphite ion, which gives a solid reaction product, if necessary after the addition of acid (to a ketone-ammonium compound reaction product) .
  • the waste liquid may be a spent ink, in which case the reactant may simply be mixed with the liquid under suitable conditions.
  • the content of alcohol and/or ketone in an ink is usually from 20 to 90% by weight, and the amount of the appropriate reactant will be chosen in order to provide at least substantially complete removal of the alcohol/ketone. Suitable amounts of reagent with respect to alcohol/ketone are 2 to 4 g/g.
  • the solid product is generally inert and non-inflammable. It can simply be separated from the liquid, and disposed of in, say, a landfill site.
  • vapour comprising MEK and/or other volatile materials may be absorbed and converted to an inert, harmless product by passing them through an on-line filter unit containing the appropriate reagent(s) in solution.
  • a suitable filter unit may be a liquid mixture or a solution absorbed by an absorbent material.
  • a two-pack kit may be formulated, each pack comprising a reagent for ketone and alcohol, respectively.
  • bisulphite ion adds to MEK.
  • the product is a white, crystalline, non-inflammable solid.
  • a suitable reagent is disodium disulphite (sodium etabisulphite, Na 2 S 2 0 5 , as supplied by BDH Chemicals, Dagenham, Essex) .
  • Polyols and alcohols react with polyisocyanates to give polyurethane polymers.
  • the product produced can vary between flexible and tough, to hard and soft, depending upon the selection of precursors and the ratio employed.
  • a catalyst can be added to speed the rate of formation of product .
  • a suitable reagent is l,3,5-tris(6-isocyanatohexyl)biuret (available as Tolonate HDB from Baxenden Chemicals, Baxenden, Lancashire) .
  • a suitable catalyst is dibutyltin dilaurate (available as Lakromark LT173 from Harcros Chemicals, Eccles, Manchester) .
  • Example 1 illustrates the invention.
  • An ink is formulated from the following components (amounts in % by weight) :
  • Dibutyltin dilaurate (0.28 g) is mixed with 680 cm 3 of thi solution.
  • Tolonate HDB (620 g) is weighed into anothe container.
  • Example 3 An ink is formulated from the following component (amounts in % by weight) :

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Emergency Management (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Business, Economics & Management (AREA)
  • Biomedical Technology (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Ink Jet (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

A waste liquid including an alcohol and/or a ketone is treated to give a solid reaction product. If alcohol is present, the fluid is contacted with a monomer-free isocyanate under conditions which give a solid polyurethane. If ketone is present, the fluid is contacted with an acid, ammonium compound or bisulphite ion under conditions which give a solid reaction product, if necessary after the addition of acid.

Description

WASTE TREATMENT Field of the Invention
This invention relates to the treatment of waste liquid or vapour containing volatile solvents, especially spent inks.
Background of the Invention
Inks, e.g. those used in ink-jet printing, comprise a mixture of inflammable solvents, primarily methyl ethyl ketone (MEK) and alcohols such as ethanol, propanol and/or butanol. The vapour given off in use is undesirable, and the spent ink is classified as hazardous waste. The disposal of hazardous waste requires specialists, and is expensive; this problem grows as environmental pressures and legislation increase the constraints on disposal. In particular, waste ink should be made inert, as soon as possible. Summary of the Invention
According to the present invention, waste liquid or vapour containing an alcohol and/or a ketone is treated in a manner which converts the hazardous component to a harmless, non-inflammable solid which can be disposed of simply and safely. The reactant for the alcohol is a monomer-free isocyanate, which can give a solid polyurethane. The reactant for the ketone is a urea, acid, ammonium compound or bisulphite ion, which gives a solid reaction product, if necessary after the addition of acid (to a ketone-ammonium compound reaction product) . Description of the Invention The waste liquid may be a spent ink, in which case the reactant may simply be mixed with the liquid under suitable conditions. The content of alcohol and/or ketone in an ink is usually from 20 to 90% by weight, and the amount of the appropriate reactant will be chosen in order to provide at least substantially complete removal of the alcohol/ketone. Suitable amounts of reagent with respect to alcohol/ketone are 2 to 4 g/g. The solid product is generally inert and non-inflammable. It can simply be separated from the liquid, and disposed of in, say, a landfill site.
The invention can also be used to treat hazardous vapour or reduce odour emission to the atmosphere, e.g. during the operation of an ink jet printer. Thus, for example, vapour comprising MEK and/or other volatile materials may be absorbed and converted to an inert, harmless product by passing them through an on-line filter unit containing the appropriate reagent(s) in solution. A suitable filter unit may be a liquid mixture or a solution absorbed by an absorbent material.
For use in the invention, a two-pack kit may be formulated, each pack comprising a reagent for ketone and alcohol, respectively.
By way of example, bisulphite ion adds to MEK. The product is a white, crystalline, non-inflammable solid. A suitable reagent is disodium disulphite (sodium etabisulphite, Na2S205, as supplied by BDH Chemicals, Dagenham, Essex) .
Polyols and alcohols react with polyisocyanates to give polyurethane polymers. The product produced can vary between flexible and tough, to hard and soft, depending upon the selection of precursors and the ratio employed. A catalyst can be added to speed the rate of formation of product . A suitable reagent is l,3,5-tris(6-isocyanatohexyl)biuret (available as Tolonate HDB from Baxenden Chemicals, Baxenden, Lancashire) . A suitable catalyst is dibutyltin dilaurate (available as Lakromark LT173 from Harcros Chemicals, Eccles, Manchester) .
The following Examples illustrate the invention. Example 1
An ink is formulated from the following components (amounts in % by weight) :
Figure imgf000005_0001
600 g sodium etabisulphite is dissolved in 1 litre o warm water to give a clear yellow saturated solution.
Dibutyltin dilaurate (0.28 g) is mixed with 680 cm3 of thi solution. Tolonate HDB (620 g) is weighed into anothe container.
Both liquids are added to 1 litre of ink in an empt plastic container. The final mixture is vigorously shake for 30 seconds and left to stand. After approximatel another 30 seconds, the ink solution becomes hot. 20-3 mins later the solution starts to solidify. There is a expansion to approximately three times the original volume, as the chemical reaction proceeds. The reaction mixture i left overnight. Next day, a flexible foam is formed. Al inflammable solvents have chemically reacted and thus bee destroyed. Example 2
The procedure of Example 1 is repeated, except tha the reaction is performed in two stages. The bisulphit solution and catalyst are added to the ink and vigorousl stirred. After 1 hour, a thin ink slurry is formed. Th Tolonate is added to this slurry and the reaction left t complete overnight. Example 3 An ink is formulated from the following component (amounts in % by weight) :
Methyl ethyl ketone 65.5
Butanol 4.5
Denatured alcohol 9.0 Distilled water 1.5
Isopropyl alcohol 2.7
Other materials 16.8 As for Examples l and 2, the ingredients are adde together or separately. For 1 litre of ink, 1120 cm3 o bisulphite solution is added together with 500 g o Tolonate and 0.82 g of the catalyst. After 2 days, a soli foam material is formed.

Claims

1. A process for the treatment of a waste liquid or vapour including an alcohol, which comprises contacting the fluid with a monomer-free isocyanate under conditions which give a solid polyurethane.
2. A process for the treatment of a waste liquid or vapour including a ketone, which comprises contacting the fluid with an acid, ammonium compound or bisulphite ion under conditions which give a solid reaction product, if necessary after the addition of acid.
3. A process for the treatment of a waste liquid or vapour including an alcohol and a ketone, which comprises contacting the fluid simultaneously or sequentially with a monomer-free isocyanate and an acid, ammonium compound or bisulphite ion under conditions which give a solid polyurethane reaction product, if necessary after the addition of acid.
4. A process according to any preceding claim, which additionally comprises separating the solid from the liquid.
5. A process according to any preceding claim, wherein the liquid is a spent ink.
6. A kit suitable for use in a process according to clai 3, which comprises a first pack comprising the acid, ammonium compound or bisulphite ion and a second pac comprising the monomer-free isocyanate and, optionally, catalyst for the polyurethane-forming reaction.
PCT/GB1991/000010 1990-01-09 1991-01-04 Waste treatment WO1991010478A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9000451.6 1990-01-09
GB909000451A GB9000451D0 (en) 1990-01-09 1990-01-09 Waste treatment

Publications (1)

Publication Number Publication Date
WO1991010478A1 true WO1991010478A1 (en) 1991-07-25

Family

ID=10669016

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1991/000010 WO1991010478A1 (en) 1990-01-09 1991-01-04 Waste treatment

Country Status (3)

Country Link
EP (1) EP0510041A1 (en)
GB (1) GB9000451D0 (en)
WO (1) WO1991010478A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2126412A1 (en) * 1971-02-27 1972-10-06 Asahi Chemical Ind
DE2719022B1 (en) * 1977-04-28 1978-08-03 Bayer Ag Process for removing formaldehyde from exhaust air
DE2739966A1 (en) * 1977-09-06 1979-03-15 Heinz Hoelter Removal of odour and toxic substances - by burning the substance absorbed on a refractory carrier
US4547350A (en) * 1983-02-09 1985-10-15 Gesser Hyman D Abatement of indoor pollutants
JPS61123639A (en) * 1984-11-19 1986-06-11 Toyota Motor Corp Treatment of organic polyisocyanate waste liquid
EP0320140A1 (en) * 1987-12-07 1989-06-14 Wormald U.S. Inc. Solidification and vapor mitigation of aldehyde spills

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2126412A1 (en) * 1971-02-27 1972-10-06 Asahi Chemical Ind
DE2719022B1 (en) * 1977-04-28 1978-08-03 Bayer Ag Process for removing formaldehyde from exhaust air
DE2739966A1 (en) * 1977-09-06 1979-03-15 Heinz Hoelter Removal of odour and toxic substances - by burning the substance absorbed on a refractory carrier
US4547350A (en) * 1983-02-09 1985-10-15 Gesser Hyman D Abatement of indoor pollutants
JPS61123639A (en) * 1984-11-19 1986-06-11 Toyota Motor Corp Treatment of organic polyisocyanate waste liquid
EP0320140A1 (en) * 1987-12-07 1989-06-14 Wormald U.S. Inc. Solidification and vapor mitigation of aldehyde spills

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Chemical Abstracts, vol. 84, no. 8, 23 February 1976, Columbus, Ohio, US), see page 374 *
Patent Abstracts of Japan, vol. 10, no. 314 (C-380)(2370), 24 October 1986; & JP-A-61123639 (TOYOTA MOTOR CORP) 11 june 1986 *
R.T. Morrison et al.: "Organic Chemistry", 3rd Edition, 1973, (Boston, US), sections 19.13, 19.14 and 32.7 see pages 638-641 *

Also Published As

Publication number Publication date
EP0510041A1 (en) 1992-10-28
GB9000451D0 (en) 1990-03-07

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