FUSIBLE OIL GEL COMPOSITIONS AND METHODS OF MAKING AND USING SAME
A gel composition is herein disclosed. According to one embodiment, the composition comprises a (i) a styrenic block copolymer, (ii) an oil; and (iii) optional additives; wherein the styrenic block copolymer comprises: a diblock polymer having a monoalkenyl arene block, designated A, a conjugated diene block, designated B, an isoprene attachment, designated i, and wherein the styrenic block copolymer can have structure ABi or iAB; the isoprene attachment i is substantially unsaturated and the conjugated diene block B is substantially saturated. The gel composition before curing exhibits thixotropic behavior, and the gel composition after curing is either solid or has a viscosity at 25° C. at a shear rate of 20 s −1 of at least 30000 mPa·s.
1 . A gel composition comprising: (i) a styrenic block copolymer, (ii) an oil; and (iii) optional additives;
wherein the styrenic block copolymer comprises:
a diblock polymer having a monoalkenyl arene block, designated A,
a conjugated diene block, designated B,
an isoprene attachment, designated i, and
wherein
the styrenic block copolymer can have structure ABi or iAB;
the isoprene attachment i is substantially unsaturated and B is substantially saturated;
wherein
the gel composition before curing has a viscosity at 25° C. at a shear rate of 20 s −1 ranging from about 5000 mPa·s to about 30000 mPa·s.; and
the gel composition after curing is either solid or has a viscosity at 25° C. at a shear rate of 20 s −1 of at least 30000 mPa·s.
2 . The gel composition of claim 1 , wherein the composition after curing has a viscosity at 25° C. at a shear rate of 20 s −1 in the range of 30000 to 500,000 mPa·s.
3 . The gel composition of claim 1 , wherein the styrenic block copolymer has a structure of ABi or iAB, and wherein the isoprene attachment i has a hydrogenation level of <50% and the conjugated diene B block has a hydrogenation level of >90%.
4 . The gel composition of claim 2 , wherein the styrenic block copolymer has a structure of ABi or iAB, and wherein the isoprene attachment i has a hydrogenation level of <40% and the conjugated diene B block has a hydrogenation level of >95%.
5 . The gel composition of claim 3 , wherein the styrenic block copolymer has a structure ABi or iAB, and wherein the isoprene attachment i has a hydrogenation level of <35% and the conjugated diene B block has a hydrogenation level of >98%.
6 . The gel composition of claim 1 , wherein at least 75% of double bonds present in the conjugated diene B block are hydrogenated.
7 . The gel composition of claim 1 , wherein from about 20% to about 60% of the double bonds in the isoprene attachment i are hydrogenated.
8 . The gel composition of claim 1 , wherein a difference in the hydrogenation level of the conjugated diene B block block and the hydrogenation level of the isoprene attachment i is greater than about 20%.
9 . The gel composition of claim 1 , wherein the styrenic block copolymer has a total residual unsaturation of from about 0.2 milliequivalents/gram to about 4 milliequivalents / gram.
10 . The gel composition of claim 1 , wherein the monoalkenyl arene A block comprises styrene, alpha-methylstyrene, para-methylstyrene, vinyl toluene, vinylnaphthalene, diphenyl ethylene, para-butyl styrene, or mixtures thereof.
11 . The gel composition of claim 1 , wherein the monoalkenyl arene A block has a polystyrene content of from about 15% to about 40%.
12 . The gel composition of claim 1 , wherein the monoalkenyl arene A block has an apparent average molecular weight of from about 5 kg/mol to about 40 kg/mol.
13 . The gel composition of claim 1 , wherein the conjugated diene B block comprises conjugated 1,3-butadiene or conjugated substituted butadienes such as, piperylene, 2,3-dimethyl-1,3 -butadiene, 1-phenyl-1,3 -butadiene or mixtures thereof
14 . The gel composition of claim 1 , wherein the conjugated diene block B has an apparent average molecular weight of from about 30 kg/mol to about 150 kg/mol.
15 . The gel composition of claim 1 , wherein the isoprene attachment i has an apparent average molecular weight of from about 2 kg/mol to about 15 kg/mol.
16 . The gel composition of claim 1 , wherein the styrenic block copolymer comprises less than about 5 wt. % of a styrenic triblock copolymer based on the total weight of the styrenic block copolymer.
17 . The gel composition of claim 1 , wherein the styrenic block copolymer is present in an amount of from about 1 wt. % to about 30 wt. % based on the total weight of the composition.
18 . The gel composition of claim 1 , wherein the oil is present in an amount of from about 70 wt. % to about 99 wt. % based on the total weight of the composition, and wherein the oil comprises a paraffin, a mineral oil, a gas-to-liquid oil, a synthetic oil, or combinations thereof.
19 . The gel composition of claim 1 , wherein the optional additives comprise an antioxidant, a metal deactivator, a curing accelerator, a rheology modifier, or combinations thereof.
20 . A method comprising making a gel composition comprising:
a) providing a styrenic block copolymer which comprises:
a diblock polymer having a monoalkenyl arene block, designated A,
a conjugated diene block, designated B, and
an isoprene attachment, designated i, and
wherein the styrenic block copolymer can have structure ABi or iAB; and
wherein i is substantially unsaturated and B is substantially saturated; and
b) providing an oil and optional additives;
c) mixing the styrenic block copolymer with the oil and optional additives;
d) curing the mixture by any of UV irradiation, thermal treatment, or both, forming an oil gel;
wherein
the gel composition before curing has a viscosity at 25° C. at a shear rate of 20 s −1 ranging from about 5000 mPa·s to about 30000 mPa·s.; and
the gel composition after curing is either solid or has a viscosity at 25° C. at a shear rate of 20 s −1 of at least 30000 mPa·s.
21 . The method of claim 20 , wherein curing of the mixture is carried out by UV irradiation in the presence of a curable functional compound selected from the group of: 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, 1,12-dodecanediol dimethacrylate, trimethylol propane triacrylate, dipentaerythritol monohydroxy-pentaacrylate or combinations thereof.
22 . The method of claim 20 , wherein curing of the composition is carried out by thermal treatment in the presence of an initiator with a half-life of from about 1 minute to about 10 minutes.
23 . The method of claim 22 , wherein the initiator comprises 2′-azobis(isobutyronitrile); 2,2′-azobis(2,4-dimethylvaleronitrile); 1,1′-azobis-(cyclohexanecarbo-nitrile); benzoyl peroxide; t-butyl 2-methylperbenzoate; dicumyl peroxide; t-butyl cumyl peroxide; di-t-butylperoxide; 1,1-di(t-butyl-peroxy)-3,3,5-trimethylcyclohexane; dilauroyl peroxide; di(2-ethylhexyl)peroxydicarbonat-e; t-amyl peroctoate; t-butyl peracetate; t-butyl perbenzoate; 2,5-bis(benzoyl-peroxy)-2,5-dimethylhexane; di-t-butyldiperoxyazelate; 1,1-di(t-butylperoxy)cyclohexane, or combinations thereof.
24 . A method comprising introducing the composition of claim 1 into an interior volume or void space of a cable, for example a fiber optic cable, and curing the composition disposed within the cable to form a solid material.