Javascript must be enabled to continue!
Polysulfide Liquid Polymers
View through CrossRef
Abstract
Polysulfide liquid polymers are a comparatively recent development conceived at the Thiokol Laboratories in 1943. The development was initiated by the problem of finding methods to reduce the molecular weight of a polysulfide rubber which was too tough to process on conventional rubber milling equipment. The problem was solved by reduction of a few of the disulfide links present in the polymer chain. It was soon found that the method was applicable to the preparation of polymers low enough in molecular weight to be liquids. The method produces dithiols of high purity which are extremely active in a wide variety of chemical reactions. Some formulations have been developed which depend on conversion from the liquid to rubber state at temperatures as low as 50° F in about 30 minutes. Most of the converting agents function through oxidation with hydrogen removal from the thiol and a linkage of sulfurs to reform the disulfide group. The converted polymers have the general properties of polysulfide polymers: good solvent resistance to a wide range of solvents, low diffusion rate of gases, good resistance to oxidation, ozone, and weathering, and a service temperature range from −65° to +250° F. (Some compounds can withstand intermittent temperatures as high as +350° F.) The low temperature properties are inherent in the polymer and do not depend on special compounding techniques.
Title: Polysulfide Liquid Polymers
Description:
Abstract
Polysulfide liquid polymers are a comparatively recent development conceived at the Thiokol Laboratories in 1943.
The development was initiated by the problem of finding methods to reduce the molecular weight of a polysulfide rubber which was too tough to process on conventional rubber milling equipment.
The problem was solved by reduction of a few of the disulfide links present in the polymer chain.
It was soon found that the method was applicable to the preparation of polymers low enough in molecular weight to be liquids.
The method produces dithiols of high purity which are extremely active in a wide variety of chemical reactions.
Some formulations have been developed which depend on conversion from the liquid to rubber state at temperatures as low as 50° F in about 30 minutes.
Most of the converting agents function through oxidation with hydrogen removal from the thiol and a linkage of sulfurs to reform the disulfide group.
The converted polymers have the general properties of polysulfide polymers: good solvent resistance to a wide range of solvents, low diffusion rate of gases, good resistance to oxidation, ozone, and weathering, and a service temperature range from −65° to +250° F.
(Some compounds can withstand intermittent temperatures as high as +350° F.
) The low temperature properties are inherent in the polymer and do not depend on special compounding techniques.
Related Results
Understanding Mg/S Batteries: The Different Electrochemistry of Lithium and Magnesium Polysulfide Solutions
Understanding Mg/S Batteries: The Different Electrochemistry of Lithium and Magnesium Polysulfide Solutions
Lithium/sulfur batteries are considered as one of the most promising post-lithium-ion battery systems, because the high specific capacity of sulfur drastically outranges the capaci...
Barrier Polymers
Barrier Polymers
AbstractBarrier polymers are used for many packaging and protective applications. As barriers they separate a system, such as an article of food or an electronic component, from an...
Barrier Polymers
Barrier Polymers
AbstractBarrier polymers are used for many packaging and protective applications. As barriers they separate a system, such as an article of food or an electronic component, from an...
Synthesis of a novel polysulfide via the reaction of a thiol compound and oxidant towards polymer self-healing application
Synthesis of a novel polysulfide via the reaction of a thiol compound and oxidant towards polymer self-healing application
Introduction: This legion is an indiscernible virtue of polysulfide that it has been employed in a range of fields. In addition, the oxidation of thiol to reversible disulfide is a...
Sulfur‐Containing Polymers
Sulfur‐Containing Polymers
AbstractThis review describes methods of synthesis and some more interesting properties of the various new sulfur‐containing polymers, with particular regard for their potential ap...
Sulfur‐Containing Polymers
Sulfur‐Containing Polymers
AbstractThis review describes methods of synthesis and some more interesting properties of the various new sulfur‐containing polymers, with particular regard for their potential ap...
Tacticity in Vinyl Polymers
Tacticity in Vinyl Polymers
AbstractVarious issues of tacticity in vinyl polymers are discussed. First, tacticity is defined and the concepts of tactic forms in polymers as a stereoregular configuration order...
Directed polymer crystallization at liquid interfaces
Directed polymer crystallization at liquid interfaces
Liquid-liquid and liquid-air interfaces are crucial to study amphiphile and colloidal self-assembly. Crystallization of polymers can also be regarded as a self-assembly process. In...

