GB664849A - Stabilised cellulose ether composition - Google Patents

Stabilised cellulose ether composition

Info

Publication number
GB664849A
GB664849A GB10179/49A GB1017949A GB664849A GB 664849 A GB664849 A GB 664849A GB 10179/49 A GB10179/49 A GB 10179/49A GB 1017949 A GB1017949 A GB 1017949A GB 664849 A GB664849 A GB 664849A
Authority
GB
United Kingdom
Prior art keywords
phosphite
tri
phenyl
cresyl
compositions
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
GB10179/49A
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.)
Acordis UK Ltd
Original Assignee
British Celanese 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 British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB664849A publication Critical patent/GB664849A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • C08K5/526Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Thermoplastic compositions comprise a thermoplastic ether of cellulose and not more than 3 per cent by weight (based on the weight of cellulose ether) of a tri-ester of phosphorous acid. The ester may be symmetrical or mixed, e.g. tri-methyl-phosphite, tri-ethyl-phosphite, tri - n - propyl - phosphite, tri - iso - propyl phosphite, tri-n-butyl-phosphite, tri-iso-butyl-phosphite, tri-ethoxyethyl-phosphite, tri-cyclohexyl-phosphite, tri-menthyl-phosphite, tri-phenyl-phosphite, tri-o-cresyl-phosphite, tri-m-cresyl-phosphite, tri-p-cresyl-phosphite, the tri-xenyl-phosphites, tri-1-naphthyl-phosphite, tri - 2 - naphthyl - phosphite, tri - (2,4 - dibrom - 1 - naphthyl) - phosphite, tri - (1,6 - dibrom - 2 - naphthyl) - phosphite, tri - 1 - anthranyl - phosphite, o - xenyl - di - phenyl - phosphite, p - tertiary - butyl - di - phenyl - phosphite, o - chloro - phenyl - diphenyl - phosphite, di - o - chloro - phenyl - carvacryl - phosphite, di - phenyl - propyl - phosphite, di - phenyl - n - butyl - phosphite, and tri - (p - tertiary - amyl - phenyl) - phosphite. Tri - aryl phosphites in which the aryl group is a benzene or alkyl-substituted benzene nucleus in which the alkyl group is a straight or branched chain or a tertiary alkyl group are preferred. Plasticizers such as dibutyl phthalate, n-butyl stearate, tri-cresyl phosphate, tri-phenyl phosphate, di-butyl sebacate, mixtures of the dimer, trimer and tetramer of polymerized styrene, or partially hydrogenated isomeric terphenyls may be present in the compositions. Lubricant plasticizers, such as refined mineral oil, may also be present. The cellulose ether may be ethyl cellulose having an ethoxyl value of 44-49 per cent. The phosphite tri-esters may be incorporated in the cellulose ether compositions by mixing them with ethyl cellulose in flake form prior to colloidalization, they may be dissolved or suspended in the plasticizers employed and the solution thus obtained mixed with ethyl cellulose, or they may be mixed with solutions of ethyl cellulose in volatile solvents such as may be employed in the preparation of films by casting. Alternatively, the esters may be added directly to a plastic mixture of cellulose ether and plasticizing agent while it is being colloidalized at elevated temperatures on hot rolls, or in a mill or mixer. The invention may be applied to the preparation of moulding and extrusion compositions and of films, foil, sheets, rods and tubes made by methods employing solvents and lower temperatures than prevail in moulding or extrusion. In an example, five ethyl cellulose compositions are prepared by mixing 100 parts by weight of ethyl cellulose (ethoxyl value 44.6 per cent) with 15 parts of dibutyl-phthalate and to each of four of these compositions are added 1, 2 and 3 parts of tri-cresyl-phosphite and 2 parts of tri-phenyl-phosphite respectively, while no phosphite is added to the fifth. The mixtures are dried, moulded at 200 DEG C. to form discs and the "yellowness coefficient" of the discs compared. Other examples are given of the preparation of moulding powders from ethyl cellulose, the same and other plasticizers and tri-phenyl, tri-cresyl, and p-tertiary-amyl-phenyl phosphites. In some cases the moulding powder (either baked or unbaked) is moulded into discs and data furnished for their "yellowness coefficient," the viscosities of comparable solutions prepared from the discs and the period required to produce crazing of the surface of the discs when exposed to "Weatherometer" tests. In two of the examples data are also given for notched Izod impact strengths of moulded bars before and after ageing at 140 DEG F. In a further example, a film is prepared by casting a solution consisting of 100 parts by weight of ethyl cellulose, 1 of dibutyl-phthalate and 1 of tri-cresyl-phosphite dissolved in 300 parts by weight of an 80/20 by volume mixture of toluene and ethyl alcohol. The degree of polymerization retained after ageing in oxygen at 200 DEG F. for 120 and 420 hours is estimated by measuring the viscosities of comparable dilute solutions of the material and compared with that of films prepared from solutions containing no phosphite. The addition of up to 3 per cent of the phosphite is said to increase the stability and resistance to the action of heat, light and air of cellulose ether compositions, particularly with respect to colour retention, brittleness and surface changes.
GB10179/49A 1948-04-16 1949-04-14 Stabilised cellulose ether composition Expired GB664849A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US664849XA 1948-04-16 1948-04-16

Publications (1)

Publication Number Publication Date
GB664849A true GB664849A (en) 1952-01-16

Family

ID=22069787

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10179/49A Expired GB664849A (en) 1948-04-16 1949-04-14 Stabilised cellulose ether composition

Country Status (1)

Country Link
GB (1) GB664849A (en)

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