GB802655A - Process for the production of aromatic disulphonyl hydrazides and their use as gas producing compositions - Google Patents
Process for the production of aromatic disulphonyl hydrazides and their use as gas producing compositionsInfo
- Publication number
- GB802655A GB802655A GB36581/56A GB3658156A GB802655A GB 802655 A GB802655 A GB 802655A GB 36581/56 A GB36581/56 A GB 36581/56A GB 3658156 A GB3658156 A GB 3658156A GB 802655 A GB802655 A GB 802655A
- Authority
- GB
- United Kingdom
- Prior art keywords
- disulphonyl
- naphthalene
- hydrazide
- chloride
- hydrazine
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/10—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
- C08J9/104—Hydrazines; Hydrazides; Semicarbazides; Semicarbazones; Hydrazones; Derivatives thereof
- C08J9/105—Hydrazines; Hydrazides; Semicarbazides; Semicarbazones; Hydrazones; Derivatives thereof containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Naphthalene-1 : 5-disulphonyl hydrazide, prepared by reacting naphthalene-1 : 5-disulphonyl chloride with hydrazine (see Group IV (b)), is used as a blowing agent in synthetic rubber and resinous plastic compositions to produce closedcell sponges. In examples: (1) a mixture of butadiene-styrene copolymers, hydrated calcium silicate, soft clay, benzothiazyl disulphide, di-orthotolylguanidine, sulphur, stearic acid, zinc oxide and naphthalene-1 : 5-disulphonyl hydrazide are mixed and cured in a mould to produce a sponge composition; (2) a chloroprene polymer containing thiuram compounds, stearic acid, benzothiazyl disulphide, silica and naphthalene - 1 : 5 - disulphonyl hydrazide are mixed and cured as in (1); (3) polyvinyl chloride, dioctyl phthalate, barium cadmium laurate and naphthalene - 1 : 5 - disulphonyl hydrazide are mixed and cured as in (1).ALSO:Aromatic disulphonyl hydrazides are prepared by mixing an aromatic disulphonyl chloride with a dilute aqueous solution of hydrazine, allowing the mixture to react at a temperature below the decomposition temperature of the required disulphonyl hydrazide, adding a strong base (as defined below) to the mixture to neutralize the hydrochloric acid formed during the reaction, and separating the resultant aromatic disulphonyl hydrazide, the reaction being allowed to continue until substantially all the free hydrazine has reacted before the strong base is added, the strong base freeing the hydrazine from the hydrazine hydrochloride formed during the reaction for further reaction with unreacted aromatic disullhonyl chloride and being added slowly so that a yield of at least 90 per cent is obtained. The "strong base" is defined as an alkali or alkaline earth metal hydroxide. The preferred product is naphthalene - 1 : 5 - disulphonyl hydrazide which is used as a blowing agent in natural and synthetic rubbers and in resinous plastics (see Groups IV (a) and V). It is preferably made from naphthalene-1 : 5-disulphonyl chloride obtained by the process described in Specification 802,654. In an example, naphthalene-1 : 5-disulphonyl chloride is slowly added to an aqueous solution of hydrazine and sodium hydroxide solution is added slowly after one hour, the mixture being stirred for three hours and the naphthalene-1 : 5-disulphonyl hydrazide obtained by filtration.ALSO:Naphthalene-1 : 5-disulphonyl hydrazide, prepared by reacting naphthalene-1 : 5-disulphonyl chloride with hedrazine (see Group IV(b)), is used as a blowing agent in rubber and resinous compositions to produce closed-cell sponges.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US802655XA | 1954-02-09 | 1954-02-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB802655A true GB802655A (en) | 1958-10-08 |
Family
ID=22156268
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB36581/56A Expired GB802655A (en) | 1954-02-09 | 1955-02-07 | Process for the production of aromatic disulphonyl hydrazides and their use as gas producing compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB802655A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000078851A1 (en) * | 1999-06-17 | 2000-12-28 | The Dow Chemical Company | Polymer foam and method of making using oil-containing furnace black as an insulation enhancer |
-
1955
- 1955-02-07 GB GB36581/56A patent/GB802655A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000078851A1 (en) * | 1999-06-17 | 2000-12-28 | The Dow Chemical Company | Polymer foam and method of making using oil-containing furnace black as an insulation enhancer |
US6258865B1 (en) | 1999-06-17 | 2001-07-10 | The Dow Chemical Company | Polymer foam and method of making using oil-containing furnace black as an insulation enhancer |
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