GB2093050A - Pipe sealing compositions - Google Patents
Pipe sealing compositions Download PDFInfo
- Publication number
- GB2093050A GB2093050A GB8203602A GB8203602A GB2093050A GB 2093050 A GB2093050 A GB 2093050A GB 8203602 A GB8203602 A GB 8203602A GB 8203602 A GB8203602 A GB 8203602A GB 2093050 A GB2093050 A GB 2093050A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sealant
- polysulphide
- formulation
- pipe
- polymer
- 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- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1012—Sulfur-containing polymers, e.g. polysulfides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/04—Polysulfides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/02—Inorganic compounds
- C09K2200/0239—Oxides, hydroxides, carbonates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Sealing Material Composition (AREA)
Abstract
A method of sealing pipe joints against leakage after installation comprises the location of a mould around or within the pipe in the region of the leaking joint and thereafter introducing a polysulphide sealant composition into the mould which is allowed to set. The sealant is a formulation of a polysulphide compound which is initially flowable but sets to an elastomeric sealing composition after a time period. The sealant composition may be in two parts which are mixed before use and may contain, beside the polysulphide,
Description
SPECIFICATION
Pipe sealing
This invention relates to a method of pipe sealing. It is more specifically, but not exclusively, directed towards the sealing of joints between sections of gas carrying pipes.
It is known to seal leaking gas joints by clamping a rigid mould or flexible mould around the joint which serve to define an annular mould cavity into which a sealant compound is introduced which thereafter hardens or sets to form a bonded collar which seals the leak externally of the pipe.
Various sealant compounds have been used to seal leaking joints in this manner. In particular polyurethanes have been used to a major extent and to a lesser degree epoxy resins, polyesters and butyl mastics. All have disadvantages which renders their usage less than ideal.
Such known sealants have proved to have low resistance to long term (50 years) vibration, deflection, distortion loads and environmental resistance is uncertain. Further problems have arisen from poor adhesion to pipes and joint materials and these sealants have been susceptible to minute, non-visible moisture levels at the application stage which requires priming or air drying. Polyurethanes incorporate isocyanates which present toxic hazards and the reactions during mixing have been highly exothermic with associated dangers to the operator. Polyurethanes are oil based products which can be costly.
It is further known to use filled and extended polyurethane sealants which incorporate calcium carbonate filler and pitch or coal tar extender. Such formulations are difficult to repeat due to quality variations depending on the source.
Thus a problem arises in providing a sealant composition which avoids at least some of these disadvantages. Polysulphide polymers are known per se but have always been of thick consistency and unable to flow and could not therefore be considered as pipe sealant formulations.
It is an object of the present invention to provide a flowable sealant for pipes which has improved characteristics and substantially avoids the disadvantages of polyurethane sealants.
Accordingly the invention provides a method of sealing joints between sections of pipes using a polysulphide pipe sealant formulation which is initially flowable and thereafter sets after a time period.
The polysulphide may be a two part mix but it is to be initially flowable and hence pourable into a mould located around or within a pipe under normal in situ conditions to seal the leaking pipe or joint.
The invention further provides a method of sealing a pipe, in which method a mould is located around or within the pipe to define an annular cavity into which a sealant formulation is introduced, the formulation thereafter setting to produce a band of sealant, the method being characterised by the use of a polysulphide formulation which is initially flowable and sets after a time period.
By the use of selected additives a polysulphide elastomer has been produced which has the required initial flowability characteristic.
Example
A two part mix of the following composition produces, by way of an example a polysulphide elastomer which is initially flowable and sets to form an effective and advantageous pipe sealant.
Part I % by weight
Polysulphide Polymer 50.0
Anti-corrosive pigments 1.2
White pigment 1.2
Chalk filler 39.0
Toluene 8.0
Mixtures of Silanes s amine phenol 0.6
100.0
Part I % by Weight
Polysulphide Polymer 50.0
Anti-corrosive pigments 1.2
White pigment 1.2
Chalk filler 39.0
Toluene 8.0
Mixtures of Silanes 8 amine phenol 0.6
100.0
The polysulphide polymer forms 25% of the mixed product which is cured ot hardened by the manganese dioxide in Part II. Use of the white pigment enables the operator to determine when mixing is complete by virtue of an overall grey appearance. The toluene acts as a thinner, solvent or diluent which evaporates during the hardening process.
The above parts I and II are thoroughly mixed and poured into a mould securely locatd about the pipe being sealed. After a period of time the formulation sets to form a leak sealing polysulphide elastomer which prevents gas seepage from the leaking pipe or joint.
The advantages obtained by use of polysulphide polymer to form an elastomer for sealing pipes are good long term performance, the mixing operation does not produce a highly exothermic reaction, there are no toxic isocyanates in the formulation and there are no toxic properties presently known of these ingredients. This formulation adheres excellently to the pipes and joints without priming and in particular the efficiency of the sealant is not reduced by moisture. The tolerance to water is excellent before, during and after application of the polysulphide formulation.
Claims (10)
1. A pipe sealant formulation incorporating a polysulphide polymer which is initially pourable at ambient temperatures and sets after a time period to form a polysulphide elastomer.
2. A sealant according to Claim 1, comprising a two part formulation, a first part consisting of poly sulphide polymer admixed with a filler, the second part incorporating a suspending medium.
3. A two part sealant according to Claim 2, comprising a first part of polysulphide polymer, chalk filler, diluent, silanes and amino phenol and a second part of curing agent, suspending medium, tetramethyl guanidine and silane.
4. A two part sealant according to Claim 3, comprising in percentage by weight a first part of polysulphide polymer 50, anti-corrosive pigments 1.2, white pigment 1.2, chalk filler 39, toluene 8, mixtures of silanes and amino phenol 0.6 and a second part of manganese dioxide 60.2, low molecular weight suspending medium 39, tetramethyl guanidine 0.4 and silane 0.4.
5. A method of sealing a pipe wherein a mould is located around or within the pipe to define an annular cavity into which a sealant compound is introduced, the compound thereafter setting to produce a band of sealant, in which method the sealant is a formulation incorporating a polysulphide polymer which is initially pourable at ambient temperatures and sets after a time period to form a polysulphide elastomer.
6. A method according to Claim 5, wherein the sealant comprises a two part formulation, a first part consisting of polysulphide polymer admixed with a filler, the second part incorporating a curing agent and a suspending medium.
7. A method according to Claim 5, wherein the sealant comprises the formulation of Claim 3.
8. A method according to Claim 5, wherein the sealant comprises the formulation of Claim 4.
9. A method of sealing joints between sections of pipes using a polysulphide polymer formulation substantially as herein described.
10. The polysulphide pipe sealant formulation herein described and exemplified.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8203602A GB2093050A (en) | 1981-02-12 | 1982-02-08 | Pipe sealing compositions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8104441 | 1981-02-12 | ||
GB8203602A GB2093050A (en) | 1981-02-12 | 1982-02-08 | Pipe sealing compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB2093050A true GB2093050A (en) | 1982-08-25 |
Family
ID=26278420
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8203602A Withdrawn GB2093050A (en) | 1981-02-12 | 1982-02-08 | Pipe sealing compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2093050A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5244956A (en) * | 1988-08-09 | 1993-09-14 | Lockheed Corporation | Corrosion inhibiting coating composition |
US5412069A (en) * | 1993-07-30 | 1995-05-02 | Rutgers, The State University Of New Jersey | Two-part polysulfide molding composition and process |
-
1982
- 1982-02-08 GB GB8203602A patent/GB2093050A/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5244956A (en) * | 1988-08-09 | 1993-09-14 | Lockheed Corporation | Corrosion inhibiting coating composition |
US5412069A (en) * | 1993-07-30 | 1995-05-02 | Rutgers, The State University Of New Jersey | Two-part polysulfide molding composition and process |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |