US2662019A - Pipe jointing composition - Google Patents
Pipe jointing composition Download PDFInfo
- Publication number
- US2662019A US2662019A US215630A US21563051A US2662019A US 2662019 A US2662019 A US 2662019A US 215630 A US215630 A US 215630A US 21563051 A US21563051 A US 21563051A US 2662019 A US2662019 A US 2662019A
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- Prior art keywords
- sulfur
- composition
- joint
- briquette
- days
- 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 - Lifetime
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- 239000000203 mixture Substances 0.000 title description 26
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 25
- 239000011593 sulfur Substances 0.000 description 25
- 229910052717 sulfur Inorganic materials 0.000 description 25
- 239000004484 Briquette Substances 0.000 description 12
- 230000007797 corrosion Effects 0.000 description 11
- 238000005260 corrosion Methods 0.000 description 11
- 229910001018 Cast iron Inorganic materials 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 150000003464 sulfur compounds Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 7
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 3
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 3
- DMYOHQBLOZMDLP-UHFFFAOYSA-N 1-[2-(2-hydroxy-3-piperidin-1-ylpropoxy)phenyl]-3-phenylpropan-1-one Chemical compound C1CCCCN1CC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 DMYOHQBLOZMDLP-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920001079 Thiokol (polymer) Polymers 0.000 description 2
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 2
- 229940083898 barium chromate Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 150000001845 chromium compounds Chemical class 0.000 description 2
- 231100001010 corrosive Toxicity 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- PXLIDIMHPNPGMH-UHFFFAOYSA-N sodium chromate Chemical compound [Na+].[Na+].[O-][Cr]([O-])(=O)=O PXLIDIMHPNPGMH-UHFFFAOYSA-N 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001600451 Chromis Species 0.000 description 1
- 102000005298 Iron-Sulfur Proteins Human genes 0.000 description 1
- 108010081409 Iron-Sulfur Proteins Proteins 0.000 description 1
- KFFQABQEJATQAT-UHFFFAOYSA-N N,N'-dibutylthiourea Chemical compound CCCCNC(=S)NCCCC KFFQABQEJATQAT-UHFFFAOYSA-N 0.000 description 1
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011396 hydraulic cement Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- MAQCMFOLVVSLLK-UHFFFAOYSA-N methyl 4-(bromomethyl)pyridine-2-carboxylate Chemical compound COC(=O)C1=CC(CBr)=CC=N1 MAQCMFOLVVSLLK-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/36—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing sulfur, sulfides or selenium
Definitions
- This invention relates to an improved sulfu pipe jointing composition adapted for use in pipejoints of the poured type.
- Molten sulfur alone and with admixtures has been used for some time for jointing various materials. These compositions have been used throughout the world under various proprietary names and have been successfully used in this country for 50 years. One of the most successful compositions is that having a composition as follows: 58.8% sulfur, 38% graded silica aggregate of which 90% passes through a 325 mesh screen, 2% carbon black and 1.2% Thiokol. This composition has been used successfully for years in jointing cast iron watermains. This composition greatly reduces initial leakage and has a great resistance to vibration and thermal shock.
- An object of this invention is to provide an improved sulfur composition for jointing pipes in which corrosion of the pipe at the interface between the sulfur compound and the pipe is eliminated.
- Another object of this invention is to provide an improved sulfur composition for jointing pipes in which the iron sulfide ring usually formed in this type of a joint is eliminated.
- a laboratory method has been developed which gives a good insight into the performance of sulfur jointing compositions in cast iron pipes.
- a piece of cast iron such as a nail is inserted in a figure eight briquette filled with a sulfur jointing composition and the time for corrosion to take place at the interface between the cast iron piece and the sulfur composition when'the figure eight briquette is immersed in various solutions is measured.
- the figure eight briquette employed is identical with that used in the A. S. T. M. standard method for determining tensile strength of hydraulic cement mortars.
- the briquette-gang mold is disclosed on pages 144-146 of the A. S. T. M. Standards 1949.
- chromium compounds accomplished the object of this invention.
- Various chromium compounds may be employed, examples of which are chromi'c oxide which may react with water to give chromic acid; zinc chromate, lead chromate, barium chromate; sodium chromate and sodium dichromate.
- the quantity of chromic acid or chromates which may be added to the sulfur composition is variable and the range. of 0.5 to by weight of the sulfur composition is preferred.
- Example 1 A mixture of 58.8% sulfur, 38.8% graded silica aggregate, 2% carbon and 1.2% Thiokol was heated and poured in a figure eight briquette. While this material was still molten, av cast iron piece was inserted and allowed to be exposed above the surface. When this was placed in water at a pH of 6, the briquette cracked in 157 days. When this was repeated at a pH. of 9, the briquette cracked. in days.
- Example 2 Example 1 was repeated except that 2% sodium chloride was added to the sulfur composition. In this test the briquette cracked in 4.6 days at a pH of 6.
- Example 3 Example 1 was repeated except that 1% lead chromate was added to the sulfur composition. In this test no cracking took place and the cast iron piece was not corroded off after 250 days;
- Example 4 Example 1 was repeated except that 5% zinc chromate was added to the sulfur composition.
- Example 5 Example 1 was repeated except that 3% chromic acid was added to the sulfur composition. In this test no noticeable change had taken place after 250 days. Similar effects were had with 1 and 5% chroniic acid.
- Example 6 Example 1 was repeated except that 3% sodium chromate was added to the sulfur composition. In this test no change had taken place after 200 days in tap water even in the presence of sodium chloride.
- Example 7 Asulfur composition similar to that employed Example 1 to which 3% chromic acid was added was used to pour a pipe joint in the usual manner. .This joint was immediately put under pressure and there was a small amount of water lost during the first few hours but the pipe joint sealed completely within 2 days. There was no black iron sulfide ring observable when the joint was out apart and inspected.
- Example 8 To the sulfur composition employed in Example 1 was added 2% chromic acid and 1% lead chromate and a joint was poured in a 4" cast iron watermain in the usual manner. This joint showed no leakage after 2 days under a pressure of p. s. i. This joint was subjected to a 5 head of water for 18 months and showed no leakage. At this time, the joint was cut apart and no pitting or any corrosion of any kind was noted at the interface between the sulfur compound and the pipe. r v
- a pipe jointing composition which consists essentially of a major proportion of sulfur, a silica aggregate and a compound of chromium selected from the group consisting of chromic acid, zinc chromate, lead chromate, barium chromate, sodium chroinate and sodium dichroniate, said compound of chromium being in the range of from about 0.5 to about 5% of the total weight of the sulfur and the aggregate.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
Patented Dec. 8, 1953 2,662,019 PI'PE JOINTING COMPOSITION Raymond B. Seymour, Allentown, and Walter R. Pascoe, Reading, Pa., assignors to The Atlas Mineral Products Company of Pennsylvania, Mertztown, Pa., a corporation of Pennsylvania No Drawing. Application March 14, 1951, Serial No. 215,630
1 Claim.
This invention relates to an improved sulfu pipe jointing composition adapted for use in pipejoints of the poured type.
Molten sulfur alone and with admixtures has been used for some time for jointing various materials. These compositions have been used throughout the world under various proprietary names and have been successfully used in this country for 50 years. One of the most successful compositions is that having a composition as follows: 58.8% sulfur, 38% graded silica aggregate of which 90% passes through a 325 mesh screen, 2% carbon black and 1.2% Thiokol. This composition has been used successfully for years in jointing cast iron watermains. This composition greatly reduces initial leakage and has a great resistance to vibration and thermal shock.
The sealing of this type of joint presumably depends upon a reaction between sulfur and iron in the presence of water, possibly to form iron sulfide. In properly constructed joints, a thin ring of black material is observed at the ironsulfur interface and there is no noticeable progression in the depth of this thin ring during years of service. However, if the joint is not properly poured or if there is settling of the ground, leaking of the joint will take place until sufficientaction between the sulfur and the iron has ensued to cause a rescaling of the joint. This type of action is generally not detrimental to the life of the pipe but if there is continued settling of the ground or vibration so that the resealing process must take place at frequent intervals, enough iron may be used up in the reaction to decrease the length of service of the pipe. Further, if corrosives such as sodium chloride are presentin the water or in the sulfur compound, severe corrosion will take place at the joint. 7
An object of this invention is to provide an improved sulfur composition for jointing pipes in which corrosion of the pipe at the interface between the sulfur compound and the pipe is eliminated.
Another object of this invention is to provide an improved sulfur composition for jointing pipes in which the iron sulfide ring usually formed in this type of a joint is eliminated.
A laboratory method has been developed which gives a good insight into the performance of sulfur jointing compositions in cast iron pipes. In these tests, a piece of cast iron such as a nail is inserted in a figure eight briquette filled with a sulfur jointing composition and the time for corrosion to take place at the interface between the cast iron piece and the sulfur composition when'the figure eight briquette is immersed in various solutions is measured. The figure eight briquette employed is identical with that used in the A. S. T. M. standard method for determining tensile strength of hydraulic cement mortars. The briquette-gang mold is disclosed on pages 144-146 of the A. S. T. M. Standards 1949. When the briquette filled with sulfur jointing composition and having a cast iron piece inserted therein is immersed in a corrosive solution, there are generally two effects; either the cast iron piece is completely corroded off at the interface or the sulfur compound is split open at this point. It is believed that the latter phenomenon is the result of excessive corrosion. Using this method, it was found that standard salt-free sulfur jointing compounds would last -200 days at a pH of 6-8 before the nail would be completely corroded off or before any cracking would take place. However, if 5% sodium chloride is added to the sulfur compound, the time for cracking is reduced to 40 days. Since it is a well established fact that corrosion with sulfur compounds is accelerated in the presence of sodium chloride, it was reasoned that if a material could be found to extend the time of complete corrosion or cracking, that such a material would have a similar effect in sulfur jointing compositiom. This is particularly important since due to the shortages of lead, it is essential to use sulfur jointing compositions wherever possible and to ascertain that such materials will outlast the cast iron pipe. In the series of experiments to be described, many compounds were tested but only a few proved to be of interest using the criterion previously cited. Metallic powders such as aluminum, lead, iron and zinc, as well as most of the saits of these materials, did not decrease corrosion in any way. For example, the addition of 5% aluminum oleate allowed the material to crack in a shorter time as 40 days. Similar effects were noted with aluminum phosphate, aluminum stearate and calcium stearate. Well known inhibitors such as dibutyl thiourea and diethyl thiourea appeared to lengthen the time somewhat but these products decreased the strength of the sulfur compound to the point where it was not of practical value. Likewise, sodium benzoate which is also a well known corrosion inhibitor was without effect, regardless of concentration. Sodium benzoate appeared to inhibit rust formation but greatly accelerated the formation of a black ring which is presumably iron sulfide,
Among the many other materials tried were various clays, triethanol amine, and phosphoric acid but none of these materials decreased the corrosion. For example, the addition of as little as 3% Bentonite caused the briquette to crack in tap water in 35 days. In this case, the cracking was very violent and caused the briquette to shatter. However, the addition of chromium compounds accomplished the object of this invention. Various chromium compounds may be employed, examples of which are chromi'c oxide which may react with water to give chromic acid; zinc chromate, lead chromate, barium chromate; sodium chromate and sodium dichromate.
The utility of this invention cannot be ex plained completely since in actual pipe joints, it would take from 40 to 50 years to prove Success or failure. However, if the tests previously de: scribed are significant, it can be predicted that the life of sulfur joints has been increased by at least several hundred percent.
To prove that the corrosion resistant efiect obtained by the addition of chromic acid or chromates to the sulfur compound was permanent and not due to a leaching out of soluble chromates, the test using the figure eight briquette was conducted in running water. By analyzing the water it was shown that no chromates were being extracted.
The quantity of chromic acid or chromates which may be added to the sulfur composition is variable and the range. of 0.5 to by weight of the sulfur composition is preferred.
The invention will be further illustrated by the following examples.
Example 1 A mixture of 58.8% sulfur, 38.8% graded silica aggregate, 2% carbon and 1.2% Thiokol was heated and poured in a figure eight briquette. While this material was still molten, av cast iron piece was inserted and allowed to be exposed above the surface. When this was placed in water at a pH of 6, the briquette cracked in 157 days. When this was repeated at a pH. of 9, the briquette cracked. in days.
Example 2 Example 1 was repeated except that 2% sodium chloride was added to the sulfur composition. In this test the briquette cracked in 4.6 days at a pH of 6.
Example 3 Example 1 was repeated except that 1% lead chromate was added to the sulfur composition. In this test no cracking took place and the cast iron piece was not corroded off after 250 days;
Example 4 Example 1 was repeated except that 5% zinc chromate was added to the sulfur composition.
In this test the briquette was unchanged after 300 days.
Example 5 Example 1 was repeated except that 3% chromic acid was added to the sulfur composition. In this test no noticeable change had taken place after 250 days. Similar effects were had with 1 and 5% chroniic acid.
Example 6 Example 1 was repeated except that 3% sodium chromate was added to the sulfur composition. In this test no change had taken place after 200 days in tap water even in the presence of sodium chloride.
Example 7 Asulfur composition similar to that employed Example 1 to which 3% chromic acid was added was used to pour a pipe joint in the usual manner. .This joint was immediately put under pressure and there Was a small amount of water lost during the first few hours but the pipe joint sealed completely within 2 days. There was no black iron sulfide ring observable when the joint was out apart and inspected.
Example 8 To the sulfur composition employed in Example 1 was added 2% chromic acid and 1% lead chromate and a joint was poured in a 4" cast iron watermain in the usual manner. This joint showed no leakage after 2 days under a pressure of p. s. i. This joint was subjected to a 5 head of water for 18 months and showed no leakage. At this time, the joint was cut apart and no pitting or any corrosion of any kind was noted at the interface between the sulfur compound and the pipe. r v
It will be apparent to those skilled in the art that this invention is subject to wide application and the scope thereof is to be restricted only in accordance with the appended claim.
What is claimed is: j
A pipe jointing composition which consists essentially of a major proportion of sulfur, a silica aggregate and a compound of chromium selected from the group consisting of chromic acid, zinc chromate, lead chromate, barium chromate, sodium chroinate and sodium dichroniate, said compound of chromium being in the range of from about 0.5 to about 5% of the total weight of the sulfur and the aggregate.
RAYMOND B. saw/Lona. WALTER R. PASCOE.
References Cited in the file or this patent UNITED STATES PATENTS Number Name Date 1,749,541 Marr 1 Mar. 4, 1930 2,129,459 Benoit Sept. 6, 1938v 2,280,301 Ray Apr. 21, 1942 2,331,270 George Oct. 5, 1943 2,416,295 Ehle Feb. 25. 1947
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US215630A US2662019A (en) | 1951-03-14 | 1951-03-14 | Pipe jointing composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US215630A US2662019A (en) | 1951-03-14 | 1951-03-14 | Pipe jointing composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2662019A true US2662019A (en) | 1953-12-08 |
Family
ID=22803753
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US215630A Expired - Lifetime US2662019A (en) | 1951-03-14 | 1951-03-14 | Pipe jointing composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2662019A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3816185A (en) * | 1970-03-18 | 1974-06-11 | Raytheon Co | Protective coating on wire |
| US3922389A (en) * | 1972-01-07 | 1975-11-25 | Raytheon Co | Method for protectively coating magnetic wire |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1749541A (en) * | 1928-04-16 | 1930-03-04 | Zacheus M Marr | Compound for filling recesses in metal castings and the like |
| US2129459A (en) * | 1935-04-10 | 1938-09-06 | Permatex Company Inc | Leak-sealing and rust preventing composition |
| US2280301A (en) * | 1941-07-01 | 1942-04-21 | Hercules Powder Co Ltd | Sulphur composition |
| US2331270A (en) * | 1941-11-28 | 1943-10-05 | Dow Chemical Co | Protecting light metal surfaces from corrosion |
| US2416295A (en) * | 1943-08-24 | 1947-02-25 | Armstrong Cork Co | Gasket material and method of making the same |
-
1951
- 1951-03-14 US US215630A patent/US2662019A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1749541A (en) * | 1928-04-16 | 1930-03-04 | Zacheus M Marr | Compound for filling recesses in metal castings and the like |
| US2129459A (en) * | 1935-04-10 | 1938-09-06 | Permatex Company Inc | Leak-sealing and rust preventing composition |
| US2280301A (en) * | 1941-07-01 | 1942-04-21 | Hercules Powder Co Ltd | Sulphur composition |
| US2331270A (en) * | 1941-11-28 | 1943-10-05 | Dow Chemical Co | Protecting light metal surfaces from corrosion |
| US2416295A (en) * | 1943-08-24 | 1947-02-25 | Armstrong Cork Co | Gasket material and method of making the same |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3816185A (en) * | 1970-03-18 | 1974-06-11 | Raytheon Co | Protective coating on wire |
| US3922389A (en) * | 1972-01-07 | 1975-11-25 | Raytheon Co | Method for protectively coating magnetic wire |
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