GB2174708A - Material useful for hydro-insulating purposes - Google Patents

Material useful for hydro-insulating purposes Download PDF

Info

Publication number
GB2174708A
GB2174708A GB08610844A GB8610844A GB2174708A GB 2174708 A GB2174708 A GB 2174708A GB 08610844 A GB08610844 A GB 08610844A GB 8610844 A GB8610844 A GB 8610844A GB 2174708 A GB2174708 A GB 2174708A
Authority
GB
United Kingdom
Prior art keywords
weight
parts
production
per cent
additives
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.)
Withdrawn
Application number
GB08610844A
Other versions
GB8610844D0 (en
Inventor
Milan Popelka
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.)
TEPLOTECHNA OP
Original Assignee
TEPLOTECHNA OP
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
Priority claimed from CS853223A external-priority patent/CS255403B1/en
Application filed by TEPLOTECHNA OP filed Critical TEPLOTECHNA OP
Publication of GB8610844D0 publication Critical patent/GB8610844D0/en
Publication of GB2174708A publication Critical patent/GB2174708A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2207/00Properties characterising the ingredient of the composition
    • C08L2207/10Peculiar tacticity
    • C08L2207/14Amorphous or atactic polypropylene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C08L23/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • C08L23/22Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers

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

The material comprises (a) 1 to 50 parts by weight of acrylobutadiene styrene resin, a copolymer of vinyl chloride containing 8 to 30 per cent by weight of vinyl acetate, or butyl rubber, (b) 50 to 99 parts by weight of amorphous polypropylene and (c) 50 to 150 parts by weight of additives, especially mineral ones, e.g. zinc oxide. It is particularly suitable for producing roof cladding.

Description

SPECIFICATION Material, especially for hydro-insulating purposes, and a method of its production The invention relates to a material, especially for hydro-insulating purposes, e.g. for roof structures, and a method of its production.
For hydro-insulating purposes, especially for roof cladding, are used mostly materials and prefabricates based on asphalt which is relatively expensive. The production of these hydroinsulating materials and their application require much electric energy.
The aim of the invention is to avoid, or at least to mitigate, the above mentioned drawbacks.
The invention provides material which comprises 1 to 50 parts by weight of acrylobutadiene styrene, or of a copolymer of vinyl chloride containing 8 to 30 per cent by weight of vinyl acetate, or of butyl rubber, 50 to 99 parts by weight of amorphous polypropylene and 50 to 150 parts by weight of additives. It is advantageous to use mineral additives, e.g. zinc oxide. To this material may be added 10 to 100 parts by weight of waste pitch which remains after vacuum distillation in the production of dimethyl terephthalate, or a remaining base of production of beta-naphthol, or of polyphenylene oxide or their combination. The waste pitch, remaining after vacuum distillation in the production of dimethyl terephthalate includes 70 to 75 per cent by weight of carbon, 20 to 25 per cent by weight of oxygen and 4 to 5 per cent by weight of hydrogen.
The invention also provides a method for the production of this material in which after homogenizing amorphous polypropylene in a solution of chlorinated aliphatic hydrocarbons, e.g.
of trichlorethylene or aromatic hydrocarbons, or of hydrocarbons of a methane series, e.g.
hexane, or their combination, with a regeneration addition, all solvents are removed from the material by vacuum distillation or by a lengthy processing, viz. mechanical one. After additives have been added, the material is calendered in cold state at a temperature in the range of -5"C to +20 "C. Material produced in this way may be provided, after having been heated, with a supporting insert for improving physical and mechanical properties of the band, especially tension parameters. As a regeneration additive may be used e.g. acrylobutadiene styrene. As to hydrocarbons of methane series, it is advantageous to use e.g. hexane.
An advantage of the material according to the invention resides in the fact that it is produced mostly of waste raw materials, and in spite of this may be substituted for asphalt products for hydro-insulating purposes. It has a good drawing quality (breaking elongation), and its embrittlement temperature is well below 0 "C. The method according to the invention is simple and requires little electric energy.
When using this material for roof cladding it is possible to use hitherto known pastes, so that it may be applied without heating, which decreases energy requirements when building roof cladding.
A material according to the invention exhibits a long time stability with respect to weather influences, and with respect to a wide range of applied additives, it may be produced in many colours.
In order that the invention may be clearly understood and readily carried into effect, it is, by way of examples, hereinafter more fully described.
Example 1 On a semi-operational equipment were homogenized, in a solution of trichloroethylene, 70 parts by weight of amorphous polypropylene. In trichloroethylene were dissolved in advance 30 parts by weight of a regeneration additive, which was here represented by acrylobutadiene styrene. The homogenizing is carried out until a paste material is obtained. This paste material is made free from all solvents by means of a vacuum distillation in a vacuum at a pressure of 100 to 500 torr. This technological operation may be replaced by a lengthy mechanical processing of the paste material, e.g. by calendering, which is less advantageous as regards economy. After having obtained this semiproduct, which is free from solvents, additives are added, e.g. 80 parts by weight of titanium dioxide. Zinc oxide or barium sulphate may be added instead of titanium dioxide.Material produced in this way is calendered at a temperature of -5 "C to +20 "C; optimum production temperature is in the range between 0 "C to 6 "C.
This material provides the following mechanical properties: drawing quality (breaking elongation) 58%, yield point in tension 1.5 MPa, softening point 181 "C and embrittlement temperature -9 "C.
Example 2 Analogously to Example 1 there was produced a material consisting of two parts by weight of butyl rubber, 98 parts by weight of amorphous polypropylene, 140 parts by weight of zinc oxide and 30 parts by weight of waste pitch remaining after vacuum distillation in the production of dimethyl terephthalate.
This material provides drawing quality (breaking elongation) 153%, yield point in tension 0.26 MPa, softening point 170 "C and embrittlement temperature over --14"C.
Although the invention is described with reference to two examples, it is to be expressly understood that it is in no way limited to these examples, but is capable of numerous modifications within the scope of the appended claims.

Claims (6)

1. Material, especially for hydro-insulating purposes, comprising 1 to 50 parts by weight of acrylobutadiene styrene, or of a copolymer of vinyl chloride containing 8 to 30 per cent by weight of vinyl acetate, or of butyl rubber, 50 to 99 parts by weight of amorphous polypropylene and 50 to 150 parts by weight of additives, especially mineral ones, e.g. of zinc oxide.
2. Material according to Claim 1, further including 10 to 100 parts by weight of waste pitch remaining after vacuum distillation in the production of dimethyl terphthalate and including 70 to 75 per cent by weight of carbon, 20 to 25 per cent by weight of oxygen and 4 to 5 per cent by weight of hydrogen, or a remaining base from the production of beta-naphthol, or of polyphenylene oxide or their combination.
3. Method of production of the material claimed in Claim 1, wherein after homogenizing amorphous polypropylene in a solution of chlorinated aliphatic hydrocarbons, e.g. of trichloroethylene or aromatic hydrocarbons, or of hydrocarbons of the methane series, e.g. hexane, or their combination, with a regeneration additive, e.g. acrylobutadiene styrene, after a paste material has been obtained, substantially all solvents are removed from this material by vacuum distillation, or by a long lasting mechanical processing, and this material, after additives have been added, is calendered in cold state at a temperature of -5 to +20 "C to obtain the final product.
4. Method according to Claim 3, wherein the final product is heated to 60 to 120 "C and a supporting insert, made advantageously of mineral fibres, is impregnated by this material for increasing physical and mechanical properties of the material.
5. Material substantially as herein described with reference to the Examples.
6. Method of production of a material according to Claim 1, 2 or 5 substantially as herein described.
GB08610844A 1985-05-05 1986-05-02 Material useful for hydro-insulating purposes Withdrawn GB2174708A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CS853223A CS255403B1 (en) 1985-05-05 1985-05-05 Material for hydroinsulation purposes
CS323485 1985-05-05

Publications (2)

Publication Number Publication Date
GB8610844D0 GB8610844D0 (en) 1986-06-11
GB2174708A true GB2174708A (en) 1986-11-12

Family

ID=25745769

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08610844A Withdrawn GB2174708A (en) 1985-05-05 1986-05-02 Material useful for hydro-insulating purposes

Country Status (4)

Country Link
DE (1) DE3612926A1 (en)
FR (1) FR2581392A1 (en)
GB (1) GB2174708A (en)
SE (1) SE8601926L (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6156828A (en) * 1995-12-12 2000-12-05 Wickett; Steve R. Rubber base asphalt emulsion method
US20150344745A1 (en) * 2008-12-23 2015-12-03 J. Van Beugen Beheer B.V. Adhesive compound

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB865297A (en) * 1958-12-02 1961-04-12 Exxon Research Engineering Co Polyalphaolefin butyl rubber blend
GB1498129A (en) * 1974-08-08 1978-01-18 Huels Chemische Werke Ag Thermoplastic embedding agents for floor tiles

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB865297A (en) * 1958-12-02 1961-04-12 Exxon Research Engineering Co Polyalphaolefin butyl rubber blend
GB1498129A (en) * 1974-08-08 1978-01-18 Huels Chemische Werke Ag Thermoplastic embedding agents for floor tiles

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6156828A (en) * 1995-12-12 2000-12-05 Wickett; Steve R. Rubber base asphalt emulsion method
US20150344745A1 (en) * 2008-12-23 2015-12-03 J. Van Beugen Beheer B.V. Adhesive compound
US9580630B2 (en) * 2008-12-23 2017-02-28 J. Van Beugen Beheer B.V. Adhesive compound

Also Published As

Publication number Publication date
SE8601926D0 (en) 1986-04-25
SE8601926L (en) 1986-11-06
FR2581392A1 (en) 1986-11-07
DE3612926A1 (en) 1986-11-06
GB8610844D0 (en) 1986-06-11

Similar Documents

Publication Publication Date Title
NO144356B (en) METHOD AND APPARATUS FOR PREPARING HYDROGEN AND OXYGEN DURING WATER DIVISION
Doi et al. Proton and carbon-13 NMR analysis of poly (β-hydroxybutyrate) isolated from Bacillus megaterium
DE602005001430T2 (en) Uncrosslinked polyethylene foam
US4144304A (en) Process for the manufacture of sheets from a mixture of vegetable fibres and polyolefine
AU3938595A (en) Process for the preparation of condensation products of melamine
ES260550A1 (en) Crosslinking polyethylene
EP0553889A1 (en) Foaming agent compositions, and method for producing elastomeric silicone foams
US4519963A (en) Electroconductive cross-linked polyolefin foam and method for manufacture thereof
AU585709B2 (en) Process for the preparation of LMW-heparin
AU3754595A (en) Process for producing starch ester, starch ester, and starch ester composition
GB2174708A (en) Material useful for hydro-insulating purposes
WO2009062741A2 (en) Method for the production of calcium carbide on an industrial scale in a n electric low-shaft furnace
US3083175A (en) Curable composition comprising cured filler, polymerized butadiene and di-alpha-cumyl peroxide and cured products thereof
Severini et al. Environmental degradation of stabilized LDPE. Later stages
DE59007037D1 (en) Process for the production of pearl-shaped expandable styrene polymers.
EP0011748B1 (en) Process for producing polyolefin foams
AU5282699A (en) Method for producing halogen-free reactive polyisobutene
US3338852A (en) Highly filled plasticized chlorinated polyethylene-polyvinyl chloride floor covering
US3835024A (en) Method for manufacturing pitch
DE2108293A1 (en) Polyolefine - base articles - plasticised in presence of pvc
CA2305517A1 (en) Process for the production of low-molecular-weight allylamine polymer or addition salt thereof
AU2520788A (en) Process for producing styrenic polymer
KR930702327A (en) Process for preparing high purity propylene carbonate and passivated electrode
US3652728A (en) Chlorinated ethylene polymer compositions for electrical insulation
DE2131845C3 (en) Curable plastic molding compounds for the production of molded parts with increased arc resistance

Legal Events

Date Code Title Description
WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)