Hydrate decomposition inhibiting composition, coupling enhanced solid hydrate, and method for improving solid hydrate storage and transportation stability

1 . A coupling enhanced solid hydrate, comprising a solid state hydrate core and a hydrate decomposition inhibition shell layer encapsulating the solid state hydrate core,

wherein the hydrate decomposition inhibiting shell layer comprises a hydrate decomposition inhibiting composition,

the solid state hydrate core comprises a hydrate forming agent, and

the hydrate decomposition inhibiting composition comprises a starch-based surfactant that comprises a carboxymethyl starch salt and an alkyl glycoside surfactant.

2 . The coupling enhanced solid hydrate of claim 1 , wherein the starch-based surfactant in the hydrate decomposition inhibiting composition forms a hydrate protective layer.

3 . The coupling enhanced solid hydrate of claim 2 , wherein the hydrate decomposition inhibiting shell layer comprises in sequence from inside to outside: the hydrate protective layer, an adsorption-absorption protective layer formed of an adsorption-absorption agent, and an optional support material.

4 . The coupling enhanced solid hydrate of claim 3 , wherein the hydrate decomposition inhibiting shell layer further comprises an ice layer disposed over the adsorption-adsorption protective layer or disposed between the adsorption-absorption protective layer and the support material.

5 . The coupling enhanced solid hydrate of claim 1 , wherein the hydrate forming agent comprises a thermodynamic hydrate promoter and/or a kinetic hydrate promoter and optionally an auxiliary agent.

6 . The coupling enhanced solid hydrate of claim 5 , wherein the hydrate forming agent is a hydrate promotion composition comprising a composite phase change material;

wherein the hydrate promotion composition comprises a composite phase change material and a hydrate promoter;

wherein the composite phase change material comprises a phase change material, a porous matrix and a solid dispersant, the phase change material and the solid dispersant are loaded on the porous matrix;

wherein the hydrate promotion composition containing the composite phase change material has a mass content of the phase change material being 0.1%-50%, based on the total mass of the composite phase change material;

wherein a mass ratio of the phase change material, the porous matrix and the solid dispenser is 1:(1-10): (0.01-0.1);

wherein the phase change material is a glycol polymer containing one or more of C2-C4 alkyl groups;

wherein the porous matrix has a pore size of 1-10 nm, a specific surface area of 100-1,000 m 2 /g, and the porous matrix is at least one selected from the group consisting of expanded graphite, nanographite, carbon nanotubes, graphene, ordered mesoporous molecular sieves, and a metal organic framework material;

wherein the solid dispersant is at least one selected from the group consisting of attapulgite, bentonite, and talc powder;

wherein the composite phase change material is prepared by a process comprising: dissolving and/or dispersing a phase change material in a solvent, and then contacting with a solid dispersant and a porous carrier, supporting the phase change material and the solid dispersant on the porous matrix, and subsequently removing the solvent;

wherein a mass ratio of the solvent to the phase change material is 1:0.01-0.5; the contact time is 2-10 h;

wherein a mass ratio of the hydrate promoter to the composite phase change material in the hydrate promotion composition comprising the composite phase change material is 1:(0.1-10);

wherein the hydrate promotion composition comprising the composite phase change material further includes an adjuvant; and a mass ratio of the hydrate promoter to the adjuvant is 1:(0.001-0.01); and

wherein the adjuvant is selected from biosurfactants.

7 . The coupling enhanced solid hydrate of claim 6 , wherein the hydrate promoter in the hydrate promotion composition comprising the composite phase change material is one or more selected from a thermodynamic hydrate promoter and a kinetic hydrate promoter;

wherein the hydrate promoter is composed of the thermodynamic hydrate promoter and the kinetic hydrate promoter;

wherein a mass ratio of the thermodynamic hydrate promoter and the kinetic hydrate promoter is (3-4): 1;

wherein the thermodynamic hydrate promoter is at least one selected from the group consisting of methylcyclopentane, methylcyclohexane, tert-butyl methyl ether, tetrabutylammonium bromide, and tetrabutylammonium chloride; and

wherein the kinetic hydrate promoter is at least one selected from amino acid kinetic hydrate promoter, leucine, histidine, tryptophan, arginine, and glutamic acid.

8 . A method for improving solid hydrate storage and transportation stability comprising a hydrate production process, a hydrate storage and transportation process and a gas release process, wherein:

(1) the hydrate production process serves to prepare a solid state hydrate core by dispersing a hydrate forming agent in an aqueous phase to form an aqueous system, contacting a gas with the aqueous system in which the hydrate forming agent is dispersed under the hydrate formation conditions; then adding a dispersion liquid containing a starch-based surface active agent under the hydrate formation conditions to form an hydrate protective layer encapsulating the solid state hydrate core outside the solid state hydrate core to prepare a coupling enhanced solid hydrate;

wherein the starch-based surfactant comprises a carboxymethyl starch salt and an alkyl glycoside surfactant;

(2) the hydrate storage and transportation process serves to store and transport the coupling enhanced solid hydrate generated by the hydrate production process under the hydrate self-protection conditions; and

(3) the gas release process serves to decompose the coupling enhanced solid hydrate after the hydrate storage and transportation process under the hydrate decomposition conditions, and release the gas therein.

9 . The method of claim 8 , wherein a mass ratio of the carboxymethyl starch salt to the alkyl glycoside surfactant is 1:1-3; and/or,

a mass ratio of the starch-based surfactant to the dispersion liquid is 0.5-10:100; and/or,

a volume ratio of the dispersion liquid containing the starch-based surfactant to an initial aqueous system forming the solid state hydrate core is not more than 15:100; and/or,

the carboxymethyl starch salt is represented by a general structural formula of [C 6 H 7 O 2 (OH) 2 OCH 2 COOM] n , wherein M is at least one selected from the group consisting of an alkali metal element, an alkaline earth metal element and an ammonium radical; and/or,

the carboxymethyl starch salt has a weight-average molecular weight of 3,000-150,000 and a substitution degree of carboxymethyl being 0.1-1; and/or,

the alkyl glycoside surfactant is expressed by a general structural formula RO(G) n ,

wherein R is a C 8 -C 18 straight or branched chain alkyl group, G represents a saccharide unit, n represents the number of saccharide unit, wherein n is a positive integer from 1 to 3.

10 . The method of claim 8 , wherein the method further comprises: after forming the hydrate protective layer, adding an adsorption-absorption agent into the system under the conditions consisting of a temperature within an hydrate self-protective effect temperature range and a system pressure is 0.01-1 MPa higher than a phase equilibrium pressure of the hydrate at the temperature range, so as to form an adsorption-absorption protective layer encapsulating the hydrate protective layer outside the hydrate protective layer;

wherein the adsorption-absorption agent comprises a porous adsorbent material and a multi-carbon straight-chain alkane;

wherein a mass ratio of the porous adsorbent material and the multi-carbon straight-chain alkane is 0.5-10:100;

wherein the hydrate self-protective effect temperature range is 253.15K-272.15K;

wherein the hydrate phase equilibrium pressure within the hydrate self-protective effect temperature range is equal to the pressure calculated from the Chen-Guo hydrate phase equilibrium equation; and

wherein a volume ratio of the adsorption-absorption agent to the initial aqueous system forming the solid state hydrate core is not more than 15:100.

11 . The method of claim 10 , wherein the method further comprises after forming the adsorption-absorption protective layer, forming an ice layer encapsulating the adsorption-absorption protective layer outside the adsorption-absorption protective layer; and

the method further comprises after forming the ice layer, adding a support material comprising foam pores into the system, wherein the foam pores are distributed in the support material, and the support material has a compressive strength of 1-8 MPa, the foam pores have an average diameter of 50-200 μm, a specific surface area of 500-1,000 m 2 /g and a density of 0.05-0.4 g/cm 3 ;

wherein a mass ratio of the hydrate forming agent and the support material is 1:(10-500); and

wherein the support material is at least one selected from the group consisting of foam activated carbon, foamed resin and foamed silicone rubber.

12 . The method of claim 8 , wherein a mode of producing the solid state hydrate core comprises: contacting a gas in an aqueous system with the hydrate forming agent under the hydrate formation conditions; and

wherein the hydrate forming agent is selected from a hydrate promotion composition containing nanoparticle and/or a hydrate promotion composition containing a composite phase change material.

13 . The coupling enhanced solid hydrate of claim 5 , wherein the hydrate forming agent is a nanoparticle-containing hydrate promotion composition;

wherein the nanoparticle-containing hydrate promotion composition comprises a nanoparticle, a surfactant and a stabilizer, the surfactant at least comprises an amino acid amphoteric surfactant and an imidazoline-type surfactant;

wherein the nanoparticle is inorganic nanoparticle; and/or, the nanoparticle has an average particle diameter within a range of 5-500 nm;

wherein the surfactant is consisting of an amino acid amphoteric surfactant and an imidazoline-type surfactant; wherein a mass ratio of the amino acid amphoteric surfactant and the imidazoline-type surfactant in the surfactant is 1:0.1-10;

wherein the amino acid amphoteric surfactant is at least one selected from the group consisting of lauroyl glutamate and N-lauroyl sarcosinate;

wherein the imidazoline-type surfactant is at least one selected from the group consisting of 1-ethyl-3-methylimidazolium acetate and 1-ethyl-3-methylimidazolium triflate;

wherein the stabilizer is at least one selected from the group consisting of sodium 1-naphthalene sulphonate, sodium 2-amino-1-naphthalene sulphonate, sodium lignosulphonate and sodium cellulose sulphonate; and

wherein the nanoparticle-containing hydrate promotion composition comprises the nanoparticle in an amount of 5-20 parts by weight, the surfactant in an amount of 1-5 parts by weight, and the stabilizer in an amount of 0.1-1 parts by weight.

14 . The coupling enhanced solid hydrate of claim 1 , wherein the coupling enhanced solid hydrate can be stored for 18 h under the conditions of a temperature of 268.15K and a pressure of 0-0.5 MPa and the decomposed gas is recovered, wherein the gas recovery rate is not less than 82%; and/or,

the coupling enhanced solid hydrate can be stored for 18 h under the conditions of a temperature of 268.15K and a pressure of 0-0.5 MPa with a decomposition rate less than 15%.

15 . The coupling enhanced solid hydrate of claim 1 , wherein a mass ratio of the carboxymethyl starch salt and the alkyl glycoside surfactant is 1:1-3.

16 . The coupling enhanced solid hydrate of claim 1 , wherein the carboxymethyl starch salt is represented by a general structural formula of [C 6 H 7 O 2 (OH) 2 OCH 2 COOM] n , wherein M is at least one selected from the group consisting of an alkali metal element, an alkaline earth metal element and an ammonium radical; and/or,

the carboxymethyl starch salt has a weight-average molecular weight of 3,000-150,000 and a substitution degree of carboxymethyl being 0.1-1; and/or,

the alkyl glycoside surfactant is expressed by a general structural formula RO(G) n , wherein R is a C 8 -C 18 straight or branched chain alkyl group, G represents a saccharide unit, n represents the number of saccharide unit, wherein n is a positive integer from 1 to 3.

17 . The coupling enhanced solid hydrate of claim 1 , wherein the hydrate decomposition inhibiting composition further comprises an adsorption-absorption agent stored independently of the starch-based surfactant, wherein the adsorption-absorption agent comprises a porous adsorbent material and a multi-carbon straight-chain alkane; and/or,

a mass ratio of the starch-based surfactant to the adsorption-absorption agent is 0.5-10:1.

18 . The coupling enhanced solid hydrate of claim 17 , wherein a mass ratio of the porous adsorbent material to the multi-carbon straight-chain alkane is 0.5-10:100; and/or,

the porous adsorbent material is at least one selected from the group consisting of expanded graphite, nanographite, carbon nanotubes, graphene, ordered mesoporous molecular sieves and metal organic framework material; and/or,

the multi-carbon straight-chain alkane is selected from straight-chain alkane containing 5-15 carbon atoms.

19 . The coupling enhanced solid hydrate of claim 1 , wherein the hydrate decomposition inhibiting composition further comprises a support material stored independently of the starch-based surfactant, the support material comprising a foam pore, wherein the foam pore is distributed in the support material, and the support material has a compressive strength of 1-8 MPa, an average diameter of the foam pore is 50-200 μm, a specific surface area of 500-1,000 m 2 /g and a density of 0.05-0.4 g/cm 3 .