An aliphatic epoxy-terminated polysulfide polymer has the formula R″—CHOH—CH2-S—R—(Sy-R)t-S—CH2-CHOH—R″ and is formed by a process, where each R is independently chosen from branched alkanediyl or branched arenediyl groups and groups with the structure —(CH2)a-O—(CH2)b-O—(CH2)c- and about 0 to about 20% of the number of R-groups are branched alkanediyl or branched arenediyl groups and about 80 to about 100% of the number of R-groups have the structure —(CH2)a-O—(CH2)b-O—(CH2)c-, where t is from about 1 to about 60, y is an average value of from about 1.0 to about 2.5, b is an integer value of from about 1 to about 8, and a and c are independently integers from about 1 to about 10, and where each R″ is independently a particular radical where, m, n, o, p, q and r independently have a value of from about 1 to about 10.

The present disclosure provides thionated polymers, comprising one or more aromatic groups and at least one S.sub.x group, wherein x is 1-200, wherein the thionated polymer comprises about 50% by weight or less, based on the weight of the thionated polymer, of substituents on the backbone of the thionated polymer that absorb at a wavelength of about 700 to about 6200 nm. Also provided are substrates such as films, glass substrates, and optical devices comprising a thionated polymer and processes for preparing a thionated polymer described herein.

The present disclosure provides thionated polymers, comprising one or more aromatic groups and at least one S.sub.x group, wherein x is 1-200, wherein the thionated polymer comprises about 50% by weight or less, based on the weight of the thionated polymer, of substituents on the backbone of the thionated polymer that absorb at a wavelength of about 700 to about 6200 nm. Also provided are substrates such as films, glass substrates, and optical devices comprising a thionated polymer and processes for preparing a thionated polymer described herein.

A rubber composition for golf balls includes (a) a base rubber, (b) a co-crosslinking agent which is an α,β-unsaturated carboxylic acid and/or a metal salt thereof, (c) a crosslinking initiator, (d) an alcohol and (e-1) an organosulfur, and the amount of component (d) is from 0.1 to 10 parts by weight per 100 parts by weight of the base rubber (a) and the organosulfur of component (e-1) is alkylphenoldisulfide polymers represented by the specific chemical formula. When the rubber composition is used in a golf ball having a core and a cover of one or more layers encasing the core, by setting the hardness difference in the core interior hardness profile to a large value while maintaining a desired core hardness, low spin properties can be manifested on golf ball shots, enabling the flight performance of the ball to be improved.

A polyphenylene sulfide resin composition exhibits excellent initial toughness and toughness after a long-term high temperature treatment typified by a tensile elongation at break after a dry heat treatment without impairing mechanical strength, chemical resistance and electrical insulation properties. The polyphenylene sulfide resin composition includes 0.01 to 10 parts by weight of an organosilane compound and 0.01 to 5 parts by weight of a metal salt of phosphorus oxoacid based on 100 parts by weight of a polyphenylene sulfide resin, and a tensile elongation at break, which is measured in accordance with ASTM-D638 under the conditions of a tensile speed of 10 mm/min and an ambient temperature of 23° C. after treating at 200° C. for 500 hours using an ASTM No. 4 dumbbell test piece obtained by injection molding the composition, is 10% or more.

A polyphenylene sulfide resin composition exhibits excellent initial toughness and toughness after a long-term high temperature treatment typified by a tensile elongation at break after a dry heat treatment without impairing mechanical strength, chemical resistance and electrical insulation properties. The polyphenylene sulfide resin composition includes 0.01 to 10 parts by weight of an organosilane compound and 0.01 to 5 parts by weight of a metal salt of phosphorus oxoacid based on 100 parts by weight of a polyphenylene sulfide resin, and a tensile elongation at break, which is measured in accordance with ASTM-D638 under the conditions of a tensile speed of 10 mm/min and an ambient temperature of 23° C. after treating at 200° C. for 500 hours using an ASTM No. 4 dumbbell test piece obtained by injection molding the composition, is 10% or more.

A degradable polyethylene glycol derivative represented by formula (1). R.sup.1, R.sup.2, and R.sup.4 represent each independently a hydrogen atom or a hydrocarbon group having from 1 to 6 carbon atoms, and at least one of R.sup.1, R.sup.2, R.sup.3 and R.sup.4 is the hydrocarbon group; P.sup.1 is a straight-chain or branched polyethylene glycol chain having a number of ethylene glycol units of 3 or more; P.sup.2 is a straight-chain polyethylene glycol chain having a number of ethylene glycol units of 3 or more; w is an integer of 1 to 8; u is an integer of 1 to 10; X.sup.1 is a chemically reactive functional group; and Z.sup.1, Z.sup.2 and Z.sup.3 are each independently a selected divalent spacer. ##STR00001##

The present invention discloses a dyeable 1.74 resin lens and a preparation method thereof. The resin lens includes a module layer with a refractive index being 1.74, a dyeable layer with a refractive index being 1.60 is poured on an upper surface of the module layer, an upward curved degree of the dyeable layer is the same as an upward curved degree of the module layer, and a center thickness of the dyeable layer is 0.5-1.2 mm. According to the dyeable 1.74 resin lens of the present invention, a layer of dyeable 1.60plus resin lens is attached to a surface of a 1.74 lens, dyeing performance is good, a visible light transmittance can reach 10-30%, and the blank that the 1.74 lens cannot be dyed is filled.

The present invention discloses a dyeable 1.74 resin lens and a preparation method thereof. The resin lens includes a module layer with a refractive index being 1.74, a dyeable layer with a refractive index being 1.60 is poured on an upper surface of the module layer, an upward curved degree of the dyeable layer is the same as an upward curved degree of the module layer, and a center thickness of the dyeable layer is 0.5-1.2 mm. According to the dyeable 1.74 resin lens of the present invention, a layer of dyeable 1.60plus resin lens is attached to a surface of a 1.74 lens, dyeing performance is good, a visible light transmittance can reach 10-30%, and the blank that the 1.74 lens cannot be dyed is filled.

Disclosed are cross-linked polymers comprising a monomer, a cross-linker, and a sulfur moiety in the polymer backbone. Methods of making cross-linked polymers comprising a monomer, a cross-linker, and a sulfur moieity in the polymer backbone are disclosed. A metal complex, comprising a cross-linked polymer chelated to a toxic heavy metal atom or ion is disclosed. The disclosure provides a method of toxic heavy metal remediation using the cross-linked polymers. Also provided are articles and coatings comprising the disclosed cross-linked polymers.