Functional monomer comprising rare earth/metal compound, preparation method thereof, and method of using the same

Abstract

A composition of matter including a mother solution; an organic ester; an additive agent and deionized water. The mother solution includes a rare earth compound or a metal compound, an organic acid, an organic amine, and deionized water. Also provided is a method of preparing the composition of matter. The method includes: 1) heating deionized water to a temperature of 50-60° C.; adding an organic acid to the deionized water, allowing to dissolve, followed by addition of a rare earth compound or a metal compound, 2-4 hours later, adding an organic amine, heating to a temperature of 70-80° C. and holding; cooling and filtering to yield a mother solution; 2) mixing the mother solution, deionized water, and a catalyst; vacuumizing a resulting mixture, heating the mixture to a temperature of 95-125° C. and holding, following by addition of a polymerization inhibitor and an organic ester; 2-4 hours later, cooling, standing, separating.

Claims

1. A composition of matter, comprising: 1) a mother solution; 2) an organic ester; 3) an additive agent; and 4) deionized water; wherein: the mother solution comprises a metal compound, an organic acid, an organic amine and deionized water; the metal compound is an oxide, a hydroxide, or a carbonate of a metal, or a mixture thereof; the organic acid is citric acid, maleic acid, ethylenediaminetetraacetic acid (EDTA), succinic acid, adipic acid, or a mixture thereof; the organic amine is diethylamine, ethylenediamine, allylamine and diethylenetriamine, or a mixture thereof; and the organic ester is an acrylate or epoxy ester; the acrylate is ethyl acrylate, butyl acrylate, isooctyl acrylate, or a mixture thereof; the epoxy ester is epoxy fatty acid methyl ester, epoxy acrylate, or a mixture thereof.

2. The composition of matter of claim 1, wherein the metal is lanthanum, cerium, europium, terbium, neodymium, zinc, calcium, magnesium, manganese, copper, nickel, aluminum, niobium, molybdenum, ruthenium, tungsten, rhenium, or hafnium.

3. The composition of matter of claim 1, wherein the additive agent comprises a catalyst and a polymerization inhibitor; the catalyst is p-toluene sulfonic acid (PTSA), and the polymerization inhibitor is hydroquinone, toluhydroquinone (THQ), hydroquinone monomethyl ether (HQMME), 4-methoxyphenol (MEHQ), or a mixture thereof.

4. The composition of matter of claim 1, comprising, by weight, 18-28% of the mother solution; 48-58% of the organic ester; 0.1-2% of the additive agent, and the deionized water as the balance.

5. A method of preparing a composition of matter, the method comprising: 1) heating deionized water to a temperature of 50-60° C., holding the temperature for 2-4 hours; adding an organic acid to the deionized water, allowing to dissolve, followed by addition of a metal compound, 2-4 hours later, adding an organic amine, heating to a temperature of 70-80° C. and holding; cooling to approximately 25° C. and filtering to yield a mother solution; 2) mixing the mother solution, deionized water, and a catalyst in a reactor; vacuumizing the reactor, heating the reactor to a temperature of 95-125° C. and holding, following by addition of a polymerization inhibitor and an organic ester; 2-4 hours later, cooling the reactor, allowing to stand, separating a resulting product, thereby yielding a composition of matter.

6. A method for preparing an alloy material, the method comprising polymerizing the composition of matter of claim 1 with a polymer monomer.

7. A copolymerized alloy emulsion, comprising, by weight: 0.3-1% of the composition of matter of claim 1; 0.2-4.5% of acrylic acid/methacrylic acid; 1-5% of isooctyl acrylate; 2-3% of butyl acrylate or trifluoroethyl methacrylate; 1-2% of methyl methacrylate; 1-2% of acrylonitrile; 35-55% of vinylidene chloride; 1-2% of acrylic phosphate; 1-2% of glycidyl acrylate; 10-25% of an emulsifying agent; 10-20% of a first base material comprising seed emulsion; 4-10% of an initiator; and 5-10‰ of a stabilizer.

8. The copolymerized alloy emulsion of claim 7, wherein the emulsifying agent comprises, by weight, 12-18% of an emulsifier, 0.2-0.35% of a wetting agent, 0.2-0.35% of a protective adhesive and 4-6% of deionized water.

9. The copolymerized alloy emulsion of claim 8, wherein the first base material comprises, by weight, 12-18% of deionized water, 0.025-0.035% of an emulsifier, 0.025-0.035% of a wetting agent, 0.43-0.53% of a protective adhesive, 0.10-0.20% of a pH regulator, and 4-10% of the seed emulsion.

10. The copolymerized alloy emulsion of claim 9, wherein the emulsifier is a non-ionic fatty acid polyoxyethylene ether; the wetting agent is a fluorine-containing anionic surfactant or a silicon containing anionic surfactant; the protective adhesive is a phosphate anionic surfactant or a sulfonate anionic surfactant.

11. The copolymerized alloy emulsion of claim 9, wherein the seed emulsifier comprises, by weight: 0.3-1% of the functional monomer of a metal compound; 0.2-4.5% of acrylic acid/methacrylic acid; 1-5% of isooctyl acrylate; 2-3% of butyl acrylate or trifluoroethyl methacrylate; 1-2% of methyl methacrylate; 1-2% acrylonitrile; 35-55% of vinylidene chloride; 1-2% of acrylic phosphate; 1-2% of glycidyl acrylate; 16.4-24.7% of emulsifying agent; 12.45-18.80% of a second base material; and 6-10% of the initiator.

12. The copolymerized alloy emulsion of claim 11, wherein the initiator comprises an initiator A and an initiator B; the initiator A comprises an oxidant and deionized water, and the initiator B comprises a reducing agent and deionized water; the oxidant is hydrogen peroxide, ammonium persulfate, potassium persulfate, or a mixture thereof; the reducing agent is carved white powder, sodium bisulfite, sodium hydrogen phosphite, or a mixture thereof.

13. The copolymerized alloy emulsion of claim 7, wherein the stabilizer comprises, by weight, 0.1-0.5‰ of an antioxidant, 0.3-0.6‰ of an antiager, and 4-5‰ of vinylidene chloride; the antioxidant is BHT, 1010, TPP, or a mixture thereof; the antiager is UV-531, UV-9, UV-P, antioxidant H, antioxidant MB, or a mixture thereof.

14. A method of preparing the copolymerized alloy emulsion of claim 7, the method comprising: 1) Mixing monomers in proportion, adding the emulsifying agent at 17±2.5° C. and holding for 30-60 min to obtain a pre-emulsified monomer mixture; 2) Adding the first base material to a polyreactor, vacuumizing the polyreactor and stirring the first base material; setting a temperature of the polyreactor to be 50-55° C.; when the temperature of the polyreactor is 34-42° C., adding the pre-emulsified monomer mixture and the initiator to the polyreactor within 13-14 hours and calculating an addition amount of the pre-emulsified monomer mixture in every 5 min; one hour later after the pre-emulsified monomer mixture is added, adding a regulator to the polyreactor within 20-30 min and calculating an addition amount of the regulator in every 5 min; adding the initiator to the polyreactor within 17-18 hours and calculating an addition amount of the initiator in every 5 min; 1-2 hours later after the initiator is added, charging nitrogen to the polyreactor for 2-3 hours to remove unreacted monomers, cooling the polyreactor to ≤35° C., and filtering using a steel mesh to yield the copolymerized alloy emulsion.

15. A copolymerized alloy solid resin, comprising, by weight: 35-55% of a monomer mixture and a dispersant mixture; 6-9% of an initiator mixture; 1-2% of a terminator; 0.1-0.2% of a neutralizer; 0.1-0.2% of a defoamer; and 25-35% of deionized water; wherein the monomer mixture and the dispersant mixture comprises: 5-10% of the composition of matter of claim 1; 1-5% of isooctyl acrylate; 1-2% acrylonitrile; 59-83% vinylidene chloride; 1-2% of acrylic phosphate; and a dispersant as the balance; and the terminator is diethylhydroxylamine (DEHA), the neutralizer is sodium hydroxide, and the defoamer is a silane compound.

16. The copolymerized alloy solid resin of claim 15, wherein the dispersant mixture comprises, by weight, 0.1-0.2% of an emulsifier, 0.1-0.2% of a wetting agent, 0.1-2% of a dispersant, 1-3% of a pH regulator, 0.002-0.008‰ of a molecular weight regulator, and 8-16% of deionized water; the dispersant is polyvinyl alcohol; the pH regulator is ammonium bicarbonate or ammonia water; and the molecular weight regulator is β-mercapto ethanol.

17. The copolymerized alloy solid resin of claim 16, wherein the initiator mixture comprises, by weight, 0.1-0.3% of an emulsifier, 0.1-0.3% of a wetting agent, 15-20% of an initiator, the balance being the deionized water, and a total mass percentage is 100%; the initiator is di-(2-ethylhexyl)peroxydicarbonate (EHP) or diisopropyl peroxydicarbonate (IPP).

18. The copolymerized alloy solid resin of claim 17, wherein the emulsifier is a non-ionic fatty acid polyoxyethylene ether; the wetting agent is a fluorine-containing anionic surfactant or silicon-containing anionic surfactant.

19. A method of preparing the copolymerized alloy solid resin of claim 15, the method comprising: 1) Adding vinylidene chloride and acrylic phosphate to a reactor in proportion, stirring, followed by addition of the composition of matter, isooctyl acrylate, and acrylonitrile; adding the dispersant mixture, to yield dispersed monomers; and 2) Vacuumizing the reactor, charging nitrogen to the reactor, adding heated deionized water to the reactor, adding the dispersed monomers and the initiator mixture, stirring, adding the terminator, the neutralizer, and the defoamer, cooling, and obtaining the copolymerized alloy solid resin.

20. A method of preparing a packaging bottle, a packaging box, a packaging bag or a preservative film for medicine, cosmetics or food, the method comprising melting, extruding, blowing or stretching the copolymerized alloy solid resin of claim 15.

Description

DETAILED DESCRIPTIONS

(1) To further illustrate, embodiments detailing a functional monomer comprising a rare earth/metal compound and a preparation method and use thereof are described below. It should be noted that the following embodiments are intended to describe and not to limit the disclosure.

Example 1

(2) The formula of the mother solution is as follows:

(3) TABLE-US-00001 Name Deionized Citric Lanthanum water acid carbonate Diethylamine Mass 61.20% 21.70% 6.3% 10.80% percentage

(4) The preparation method is as follows:

(5) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(6) 2) Citric acid was added and completely dissolved, and then lanthanum carbonate was added.

(7) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(8) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, diethylamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 2

(9) The formula of the mother solution is as follows

(10) TABLE-US-00002 Name Deionized Maleic Cerium water acid carbonate Ethylenediamine Mass 56.60% 24.20% 8.10% 11.10% percentage

(11) The preparation method is as follows:

(12) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(13) 2) Maleic acid was added and completely dissolved, and then cerium carbonate was added.

(14) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(15) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, ethylenediamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 3

(16) The formula of the mother solution is as follows

(17) TABLE-US-00003 Name Ethylene- Deion- diamine- ized tetraacetic Cerium Lanthanum water acid carbonate carbonate Allylamine Mass 57.30% 18.50% 2.80% 5.30% 16.10% percentage

(18) The preparation method is as follows:

(19) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(20) 2) Ethylenediaminetetraacetic acid was added and completely dissolved, and then cerium carbonate and lanthanum carbonate were added.

(21) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(22) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, allylamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 4

(23) The formula of the mother solution is as follows

(24) TABLE-US-00004 Name Deionized Succinic Zinc Copper Diethylene- water acid oxide hydroxide triamine Mass 51.70% 21.20% 4.60% 4.00% 13.10% percentage

(25) The preparation method is as follows:

(26) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(27) 2) Succinic acid was added and completely dissolved, and then zinc oxide and copper hydroxide were added.

(28) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(29) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, diethylenetriamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 5

(30) The formula of the mother solution is as follows

(31) TABLE-US-00005 Name Deion- ized Adipic Magnesium Manganese water acid oxide carbonate Allylamine Mass 54.70% 22.20% 5.10% 2.30% 15.70% percentage

(32) The preparation method is as follows:

(33) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(34) 2) Adipic acid was added and completely dissolved, and then magnesium oxide and manganese carbonate were added.

(35) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(36) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, allylamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 6

(37) The formula of the mother solution is as follows

(38) TABLE-US-00006 Name Deion- ized Citric Calcium Manganese water acid hydroxide carbonate Diethylamine Mass 49.70% 24.20% 3.10% 4.30% 18.70% percentage

(39) The preparation method is as follows:

(40) 1) Deionized water was added to a flask, stirred, heated to 55° C. The temperature was held at 55±2° C. in the presence of a pH meter.

(41) 2) Citric acid was added and completely dissolved, and then calcium hydroxide and manganese carbonate were added.

(42) 3) The temperature of the mixture was controlled at 55±2° C. for 2-4 hours.

(43) 4) The change of the pH of the mixture was observed. When the pH value was stable at 2.8-3.6, the viscosity of the liquid increased. When the liquid dried slightly, diethylamine was added immediately, and the mixture was heated to 75° C., and the temperature was held at 75±2° C. for two hours. Thereafter, the mixture was cooled, filter, to yield the mother solution.

Example 7

(44) The formula of the functional monomer is as follows:

(45) TABLE-US-00007 Name Deion- Mother P-methyl- ized solution in benzene- Hydro- Ethyl water Example 1 sulfonic acid quinone acrylate Mass 25.20% 24.60% 0.20% 0.68% 49.32% percentage

(46) The preparation method of the functional monomer is as follows:

(47) 1) Deionized water, the mother solution and P-methylbenzenesulfonic acid were added to an autoclave. The autoclave was vacuumized and nitrogen charged thrice, and then was vacuumized again. The mixture was stirred, heated to 110° C. and maintained.

(48) 2) Hydroquinone and ethyl acrylate were mixed and dissolved completely.

(49) The mixture was dropwise added to the autoclave when the temperature therein was 110° C. Specifically, 0.6-0.9% of the total weight of the mixture of hydroquinone and ethyl acrylate was added every 5 minutes in 10-15 hours. The temperature was held for 3 hours.

(50) 3) The mixture was cooled to below 50° C., thereby yielding a product.

(51) 4) The product was poured to an oil-water separator. 4 hours later, a superstratum was produced and collected, which was the functional monomer.

(52) 5) A drying agent accounting for 1-3 wt. % of the functional monomer was added to the functional monomer. 24 hours later, the mixture was filtered, and stored in a dark container at room temperature. The term of validity of the functional monomer was 12 months.

Example 8

(53) The formula of the functional monomer is as follows:

(54) TABLE-US-00008 Name Deion- Mother P-methyl- ized solution in benzene- Butyl water Example 2 sulfonic acid THQ acrylate Mass 28.30% 19.50% 0.22% 0.71% 51.27% percentage

(55) The preparation method of the functional monomer is as follows:

(56) 1) Deionized water, the mother solution and P-methylbenzenesulfonic acid were added to an autoclave. The autoclave was vacuumized and nitrogen charged thrice, and then was vacuumized again. The mixture was stirred, heated to 120° C. and maintained.

(57) 2) O-methylhydroquinone (THQ) and butyl acrylate were mixed and dissolved completely. The mixture was dropwise added to the autoclave when the temperature therein was 120° C. Specifically, 0.6-0.9% of the total weight of the mixture of o-methylhydroquinone (THQ) and butyl acrylate was added every 5 minutes in 10-15 hours. The temperature was held for 3 hours.

(58) 3) The mixture was cooled to below 50° C., thereby yielding a product.

(59) 4) The product was poured to an oil-water separator. 4 hours later, a superstratum was produced and collected, which was the functional monomer.

(60) 5) A drying agent accounting for 1-3 wt. % of the functional monomer was added to the functional monomer. 24 hours later, the mixture was filtered, and stored in a dark container at room temperature. The term of validity of the functional monomer was 12 months.

Example 9

(61) The formula of the functional monomer is as follows:

(62) TABLE-US-00009 Name Deion- Mother P-methyl- ized solution in benzene- Isooctyl water Example 3 sulfonic acid HQMME acrylate Mass 22.60% 27.20% 0.25% 0.75% 49.20% percentage

(63) The preparation method of the functional monomer is as follows:

(64) 1) Deionized water, the mother solution and P-methylbenzenesulfonic acid were added to an autoclave. The autoclave was vacuumized and nitrogen charged thrice, and then was vacuumized again. The mixture was stirred, heated to 105° C. and maintained.

(65) 2) Hydroquinone monomethyl ether (HQMME) and isooctyl acrylate were mixed and dissolved completely. The mixture was dropwise added to the autoclave when the temperature therein was 105° C. Specifically, 0.6-0.9% of the total weight of the mixture of hydroquinone monomethyl ether (HQMME) and isooctyl acrylate was added every 5 minutes in 10-15 hours. The temperature was held for 3 hours.

(66) 3) The mixture was cooled to below 50° C., thereby yielding a product.

(67) 4) The product was poured to an oil-water separator. 4 hours later, a superstratum was produced and collected, which was the functional monomer.

(68) 5) A drying agent accounting for 1-3 wt. % of the functional monomer was added to the functional monomer. 24 hours later, the mixture was filtered, and stored in a dark container at room temperature. The term of validity of the functional monomer was 12 months.

Example 10

(69) The formula of the functional monomer is as follows:

(70) TABLE-US-00010 Name Deion- Mother P-methyl- ized solution in benzene- water Example 4 sulfonic acid MEHQ EFAME Mass 31.60% 18.20% 0.19% 0.70% 49.31% percentage

(71) The preparation method of the functional monomer is as follows:

(72) 1) Deionized water, the mother solution and P-methylbenzenesulfonic acid were added to an autoclave. The autoclave was vacuumized and nitrogen charged thrice, and then was vacuumized again. The mixture was stirred, heated to 105° C. and maintained.

(73) 2) 4-methoxyphenol (MEHQ) and epoxy fatty acid methyl ester (EFAME) were mixed and dissolved completely. The mixture was dropwise added to the autoclave when the temperature therein was 105° C. Specifically, 0.6-0.9% of the total weight of the mixture of -methoxyphenol (MEHQ) and epoxy fatty acid methyl ester (EFAME) was added every 5 minutes in 10-15 hours. The temperature was held for 3 hours.

(74) 3) The mixture was cooled to below 50° C., thereby yielding a product.

(75) 4) The product was poured to an oil-water separator. 4 hours later, a superstratum was produced and collected, which was the functional monomer.

(76) 5) A drying agent accounting for 1-3 wt. % of the functional monomer was added to the functional monomer. 24 hours later, the mixture was filtered, and stored in a dark container at room temperature. The term of validity of the functional monomer was 12 months.

Example 11

(77) The formula of the functional monomer is as follows:

(78) TABLE-US-00011 Name Deion- Mother P-methyl- ized solution in benzene- Dibutyl water Example 5 sulfonic acid MEHQ maleate Mass 27.40% 21.60% 0.27% 0.75% 49.98% percentage

(79) The preparation method of the functional monomer is as follows:

(80) 1) Deionized water, the mother solution and P-methylbenzenesulfonic acid were added to an autoclave. The autoclave was vacuumized and nitrogen charged thrice, and then was vacuumized again. The mixture was stirred, heated to 95° C. and maintained.

(81) 2) 4-methoxyphenol (MEHQ) and dibutyl maleate were mixed and dissolved completely. The mixture was dropwise added to the autoclave when the temperature therein was 95° C. Specifically, 0.6-0.9% of the total weight of the mixture of 4-methoxyphenol (MEHQ) and dibutyl maleate was added every 5 minutes in 10-15 hours. The temperature was held for 3 hours.

(82) 3) The mixture was cooled to below 50° C., thereby yielding a product.

(83) 4) The product was poured to an oil-water separator. 4 hours later, a superstratum was produced and collected, which was the functional monomer.

(84) 5) A drying agent accounting for 1-3 wt. % of the functional monomer was added to the functional monomer. 24 hours later, the mixture was filtered, and stored in a dark container at room temperature. The term of validity of the functional monomer was 12 months.

Example 12

(85) The functional monomers obtained in Examples 7-11 are respectively copolymerized with vinylidene chloride, thereby yield alloy materials, the parameters thereof being as follows:

(86) TABLE-US-00012 Example Example Example Example Example Ordinary Executive Term 7 8 9 10 11 PVDC Standard Tensile strength/ 104/123 123/147 136/164 143/180 169/213 65/82 BB/0012- MPa, vertical/ 2008(5.6) horizontal Elongation at 74/61 95/72 111/82  116/86  137/105  53/41 break/%, vertical/ horizontal Tear resistance/ 0.36/0.36 0.45/0.42 0.51/0.53 0.57/0.58 0.64/0.61 0.24/0.22 N, vertical/ horizontal Heat shrinkable −5/−6 −8/−8 −12/−11 −14/−14 −18/−19 −22/−21 rate/%, vertical/ horizontal Water vapor 0.8 0.8 0.9 0.9 1.1 2.2 transmission rate/g/(m.sup.2, 24 H) Oxygen 4.0 4.0 4.0 4.6 5.2 31.0 permeability/cm.sup.3/ (m.sup.2/24 h. 0.1 MPa) Thermal 135° C. 135° C. 135° C. 140° C. 150° C. 105° C. ISO 182- stability 1:1990

(87) 1. The film width was 20 mm, and the thickness was 42 m.

(88) 2. Ordinary PVDC has high brittleness and poor thermal stability, so it cannot be blown to form the film alone. It can only be combined with other polymer materials (PE, nylon) to form the film, with relatively poor experimental barrier.

(89) 3. The film materials in Examples 7-11 are formed by rare-earth elements and PVDC (REPVDC), so that the barriers are relatively high. Because the abbreviation of rare earth element in English is “Re” and “Re” has the meaning of retracing and remanufacturing in English, to distinguish the existing PVDC materials, the PVDC copolymerized with the rare earth/metal alloy is named REPVDC.

(90) The formula of the mother solution is as follows:

(91) TABLE-US-00013 Name Deionized Citric Lanthanum water acid carbonate Diethylamine Mass percentage 61.20% 21.70% 6.3% 10.80%

(92) The formula of the functional monomer is as follows:

(93) TABLE-US-00014 Name Deion- P-methyl- ized Mother benzene- Hydro- Ethyl water solution sulfonic acid quinone acrylate Mass 25.20% 24.60% 0.20% 0.68% 49.32% percentage

(94) The formula is only for example. In actual operation, the functional monomer can be prepared according to the actual demand.

Example 13

(95) The formula of the seed emulsion of the copolymerized REPVDC alloy emulsion is described as follows.

(96) The formula of the monomer mixture is as follows:

(97) TABLE-US-00015 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.32 0.52 1.10 2.40 1.20 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.40 44.84 1.20 1.40 (%)

(98) The formula of the emulsifying agent:

(99) TABLE-US-00016 Name Non-ionic Phosphate fatty acid ester Deion- polyoxy- Fluorinated based ized ethylene anionic anionic water ether surfactant surfactant Percentage 15.00 0.31 0.25 4.30 (%)

(100) The formula of the base material:

(101) TABLE-US-00017 Name Non-ionic phosphate fatty acid ester Deion- polyoxy- Fluorinated based ized ethylene anionic anionic Ammonium water ether surfactant surfactant bicarbonate Percentage 15.00 0.025 0.03 0.50 0.12 (%)

(102) The formula of the initiator:

(103) TABLE-US-00018 Name Reagent A Reagent B Hydrogen Deionized Deionized peroxide water Rongalite water Percentage (%) 0.05 5.00 0.03 5.00

(104) The preparation method of the seed emulsion is detailed as follows:

(105) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(106) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice.

(107) Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(108) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(109) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 60° C.

(110) 5) When the temperature rose to 48° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5% of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(111) 6) When the temperature rose to 52° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(112) 7) The mixture was held at 60° C. for 3 hours, and then the temperature was set to be 55° C. until the emulsified monomers were completely added.

(113) 8) One hour later, the temperature was set to be 52° C. until the initiator was completely added.

(114) 9) One hour later, the temperature of the polyreactor was decreased.

(115) 10) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(116) 11) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(117) The seed emulsion of the example has high transparency, high residue and good storage stability. The preparation process has high polymerization pressure and is easy to demulsify.

Example 14

(118) The formula of the monomer mixture is as follows:

(119) TABLE-US-00019 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.42 0.46 1.40 2.10 1.50 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.20 49.73 1.60 1.10 (%)

(120) The formula of the emulsifying agent:

(121) TABLE-US-00020 Name Non-ionic fatty acid Sulfonate Deion- polyoxy- Silicone based ized ethylene anionic anionic water ether surfactant surfactant Percentage 13.00 0.35 0.35 4.00 (%)

(122) The formula of the base material:

(123) TABLE-US-00021 Name Non-ionic polyoxy- Sulfonate Deion- ethylene Silicone based Glacial ized fatty acid anionic anionic acetic water ester surfactant surfactant acid Percentage 12.00 0.028 0.035 0.46 0.15 (%)

(124) The formula of the initiator:

(125) TABLE-US-00022 Name Reagent A Reagent B Ammonium Deionized Sodium Deionized persulfate water bisulfite water Percentage 0.07 5.00 0.05 5.00 (%)

(126) The preparation method of the seed emulsion is detailed as follows:

(127) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(128) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice.

(129) Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(130) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(131) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 55° C.

(132) 5) When the temperature rose to 43° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5% of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(133) 6) When the temperature rose to 48° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(134) 7) The mixture was held at 55° C. for 3 hours, and then the temperature was set to be 52° C. until the emulsified monomers were completely added.

(135) 8) One hour later, the temperature was set to be 50° C. until the initiator was completely added.

(136) 9) One hour later, the temperature of the polyreactor was decreased.

(137) 10) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(138) 11) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(139) The seed emulsion of the example has high barrier (long time salt spray test), low residue and moderate storage stability. The preparation process has moderate polymerization pressure, low residual monomer and high emulsion recovery rate of 99.3%.

Example 15

(140) The formula of the seed emulsion of the copolymerized REPVDC alloy emulsion is described as follows.

(141) The formula of the monomer mixture is as follows:

(142) TABLE-US-00023 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.38 3.50 4.20 3.00 1.80 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.40 36.78 1.20 1.50 (%)

(143) The formula of the emulsifying agent:

(144) TABLE-US-00024 Name Non-ionic polyoxy- Sulfonate Deion- ethylene Silicone based ized fatty acid anionic anionic water ester surfactant surfactant Percentage 15.00 0.30 0.30 4.80 (%)

(145) The formula of the base material:

(146) TABLE-US-00025 Name Non-ionic polyoxy- Sulfonate Deion- ethylene Silicone based ized fatty acid anionic anionic Diammonium water ester surfactant surfactant phosphate Percentage 15.00 0.031 0.035 0.50 0.11 (%)

(147) The formula of the initiator:

(148) TABLE-US-00026 Name Reagent A Reagent B Potassium Deionized Sodium Deionized persulfate water orthophosphite water Percentage (%) 0.10 5.00 0.06 5.00

(149) The preparation method of the seed emulsion is detailed as follows:

(150) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(151) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(152) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(153) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 55° C.

(154) 5) When the temperature rose to 48° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5% of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(155) 6) When the temperature rose to 52° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(156) 7) The mixture was held at 55° C. for 3 hours, and then the temperature was set to be 50° C. until the emulsified monomers were completely added.

(157) 8) One hour later, the temperature was set to be 48° C. until the initiator was completely added.

(158) 9) One hour later, the temperature of the polyreactor was decreased.

(159) 10) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(160) 11) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(161) The seed emulsion of the example has high adhesive strength, high barrier than that of Example 2, no residue and moderate storage stability. The preparation process has moderate polymerization pressure, high emulsion recovery rate, and lower residual monomer than that of Example 2.

Example 16

(162) The formula of the copolymerized REPVDC alloy emulsion is described as follows.

(163) The formula of the monomer mixture is as follows:

(164) TABLE-US-00027 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.43 0.20 2.10 2.80 1.60 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.20 40.25 1.00 1.00 (%)

(165) The formula of the emulsifying agent:

(166) TABLE-US-00028 Name Non-ionic phosphate fatty acid ester Deion- polyoxy- Fluorinated based ized ethylene anionic anionic water ether surfactant surfactant Percentage (%) 13.80 0.29 0.23 3.96

(167) The formula of the base material:

(168) TABLE-US-00029 Non-ionic phosphate fatty acid Fluorinated ester based Seed Deionized polyoxyethylene anionic anionic Ammonium Name emulsion water ether surfactant surfactant bicarbonate Percentage 8.2 13.00 0.023 0.027 0.46 0.11 (%)

(169) The formula of the initiator:

(170) TABLE-US-00030 Name Reagent A Reagent B Hydrogen Deionized Deionized peroxide water Rongalite water Percentage (%) 0.046 4.60 0.0276 4.60

(171) The formula of the stabilizer:

(172) TABLE-US-00031 Name Antioxidant Antideteriorant Vinylidene chloride (BHT) (UV-531) (as a solvent) Permillage (‰) 0.30 0.52 4.8

(173) The preparation method of the seed emulsion is detailed as follows:

(174) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(175) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice.

(176) Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(177) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(178) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 52° C.

(179) 5) When the temperature rose to 38° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5%0 of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(180) 6) When the temperature rose to 42° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(181) 7) The mixture was held at 52° C. until the emulsified monomers were completely added.

(182) 8) One hour later, the temperature was set to be 50° C.

(183) 9) When the temperature decreased to 50° C., the regulator was added to the polyreactor, with an addition amount of 15-17% of the total weight of the regulator in every 5 min. The addition process was to be finished in 25-35 minutes.

(184) 10) The mixture was held at 50° C. for 1 hour, and then the temperature of the polyreactor was decreased.

(185) 11) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(186) 12) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(187) The seed emulsion of the example has a wide range of particle size, high barrier, good storage stability, low residual monomer and short time to discharge the unreacted monomers. The preparation process has moderate polymerization pressure.

Example 17

(188) The formula of the copolymerized REPVDC alloy emulsion is described as follows.

(189) The formula of the monomer mixture is as follows:

(190) TABLE-US-00032 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.32 0.43 2.40 2.10 1.62 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.50 46.10 1.51 1.00 (%)

(191) The formula of the emulsifying agent:

(192) TABLE-US-00033 Name Non-ionic fatty acid Sulfonate Deion- polyoxy- Silicone based ized ethylene anionic anionic water ether surfactant surfactant Percentage (%) 11.22 0.33 0.33 3.76

(193) The formula of the base material:

(194) TABLE-US-00034 Non-ionic Sulfonate fatty acid Silicone based De- polyoxy- anionic anionic Glacial Seed ionized ethylene surfac- surfac- acetic Name emulsion water ether tant tant acid Percentage 6.40 10.28 0.026 0.033 0.43 0.14 (%)

(195) The formula of the initiator:

(196) TABLE-US-00035 Name Reagent A Reagent B Ammonium Deionized Sodium Deionized persulfate water bisulfite water Percentage (%) 0.065 4.70 0.047 4.70

(197) The formula of the stabilizer:

(198) TABLE-US-00036 Name Antioxidant Antideteriorant Vinylidene chloride (1010) (UV-P) (as a solvent) Permillage (‰) 0.30 0.52 4.8

(199) The preparation method of the seed emulsion is detailed as follows:

(200) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(201) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice.

(202) Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(203) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(204) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 50° C.

(205) 5) When the temperature rose to 36° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5% of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(206) 6) When the temperature rose to 44° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(207) 7) The mixture was held at 50° C. until the emulsified monomers were completely added.

(208) 8) One hour later, the temperature was set to be 48° C.

(209) 9) When the temperature decreased to 48° C., the regulator was added to the polyreactor, with an addition amount of 15-17% of the total weight of the regulator in every 5 min. The addition process was to be finished in 25-35 minutes.

(210) 10) The mixture was held at 48° C. for 1 hour, and then the temperature of the polyreactor was decreased.

(211) 11) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(212) 12) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(213) The seed emulsion of the example has a moderate range of particle size, high barrier, good storage stability, low residual monomer and long time to discharge the unreacted monomers. The preparation process has moderate polymerization pressure.

Example 18

(214) The formula of the copolymerized REPVDC alloy emulsion is described as follows.

(215) The formula of the monomer mixture is as follows:

(216) TABLE-US-00037 Name Functional Methacrylic Isooctyl Butyl Methyl monomer acid acrylate acrylate methacrylate Percentage 0.36 3.13 4.03 2.58 1.73 (%) Name Vinylidene Acrylic Glycidyl Acrylonitrile chloride phosphate acrylate Percentage 1.30 35.31 1.20 1.44 (%)

(217) The formula of the emulsifying agent:

(218) TABLE-US-00038 Name Non-ionic fatty acid Sulfonate Deion- polyoxy- Silicone based ized ethylene anionic anionic water ether surfactant surfactant Percentage (%) 14.40 0.28 0.28 4.61

(219) The formula of the base material:

(220) TABLE-US-00039 Non-ionic Sulfonate fatty acid Silicone based Seed Deionized polyoxyethylene anionic anionic Diammonium Name emulsion water ether surfactant surfactant phosphate Percentage 4.00 14.40 0.030 0.033 0.48 0.10 (%)

(221) The formula of the initiator:

(222) TABLE-US-00040 Name Reagent A Reagent B Potassium Deionized Sodium Deionized persulfate water orthophosphite water Percentage (%) 0.096 4.80 0.058 4.80

(223) The formula of the stabilizer:

(224) TABLE-US-00041 Name Antioxidant Antideteriorant Vinylidene chloride (TPP) (MB) (as a solvent) Permillage (‰) 0.53 0.52 4.8

(225) The preparation method of the seed emulsion is detailed as follows:

(226) 1) The monomer mixture was prepared according to the formula and added to a first reactor, stirred.

(227) 2) The emulsifying agent was prepared according to the formula and added to a second reactor. The reactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, nitrogen was charged again to make the pressure gauge zero. The emulsifying agent was stirred and the temperature was at 17±2.5° C.

(228) 3) Turn on a metering pump, and the monomer mixture was dropwise added to the second reactor in about 90 minutes, and then stirred at 17±2.5° C. for 30 minutes to obtain the emulsified monomers.

(229) 4) The base material was added to a polyreactor according to the formula. The polyreactor was sealed, vacuumized, and nitrogen charged thrice. Thereafter, the polyreactor was vacuumized again to have a pressure of −0.09-0.080. The base material was stirred under 600-800 rpm. The setting temperature was 48° C.

(230) 5) When the temperature rose to 34° C., the initiator was added to the polyreactor, with an addition amount of 4.5-5% of the total weight of the initiator in every 5 min. The addition process was to be finished in 17 hours.

(231) 6) When the temperature rose to 34° C., the emulsified monomers obtained in 3) were added to the polyreactor, with an addition amount of 5.8-6.2% of the total weight of the emulsified monomers in every 5 min. The addition process was to be finished in 14 hours

(232) 7) The mixture was held at 48° C. until the emulsified monomers were completely added.

(233) 8) One hour later, and the temperature was set to be 45° C.

(234) 9) When the temperature decreased to 45° C., the regulator was added to the polyreactor, with an addition amount of 15-17% of the total weight of the regulator in every 5 min. The addition process was to be finished in 25-35 minutes.

(235) 10) The mixture was held at 45° C. for 1 hour, and then the temperature of the polyreactor was decreased.

(236) 11) When the temperature decreased to less than 35° C., the nitrogen valve and vacuum pump switch of the polyreactor were opened to discharge the unreacted monomers. 2 hours later, samples were taken from the sampling valve to analyze the concentration of the residual monomer until the samples meet the standard, and then the nitrogen valve and vacuum pump were closed.

(237) 12) The vent valve was opened to make the pressure in the polyreactor equal to the atmospheric pressure, and then the final product was collected.

(238) The seed emulsion of the example has a narrow range of particle size, good storage stability, high resistant to UV radiation, high residual monomer and long time to discharge the unreacted monomers. The preparation process has moderate polymerization pressure.

(239) The performance of the emulsion in example 16-18 are as follows:

(240) Examples 13, 14 and 15 provide seed emulsions, which are used as seeds to mix with the base material for the polymerization of alloy emulsion. The difference between the three seed emulsions is that the molecular weight is different, and the specific relationship is: 1<2<3; in the polymerization of the alloy emulsion, the seed emulsion can be selected according to the required molecular weight.

(241) TABLE-US-00042 Executive Term Example 16 Example 17 Example 18 Standard Adhesive ≥7 Mpa ≥5 Mpa ≥5 Mpa GB/T5210- strength 85 Water vapor 1.0 0.8 1.2 BB/0012- transmission 2008(5.6) rate/g/(m.sup.2, 24 H) Oxygen 6.0 4.0 9.0 permeability/ cm.sup.3/(m.sup.2/24 h .Math. 0.1 MPa) Resistant to >200 H >200 H >500 H ISO UV radiation 11507- 2007 Note Suitable for Suitable for Suitable for waterborne waterborne waterborne anticorrosive anticorrosive anticorrosive primer of intermediate surface steel coating of coating of structure; steel steel PVDC film structure; structure; without primer primer primer coated coated PVDC film PVDC film with boiling resistance

Example 19

(242) The formula of the copolymerized REPVDC alloy solid emulsion is described as follows.

(243) The formula of the monomer mixture:

(244) TABLE-US-00043 Name Functional Isooctyl Vinylidene Acrylic monomer acrylate Acrylonitrile chloride phosphate Percentage 6.60 4.20 1.40 73.23 1.80 (%)

(245) The formula of the dispersant mixture:

(246) TABLE-US-00044 Non-ionic fatty acid Fluorinated β- Deionized polyoxyethylene anionic Polyvinyl Ammonium Mercapto- Name water ether surfactant alcohol bicarbonate ethanol Percentage 11.50 0.16 0.10 1.10 1.30 0.004% (%)

(247) The formula of the initiator mixture:

(248) TABLE-US-00045 Non-ionic fatty acid Di-2- Deion- polyoxy- Fluorinated ethylhexyl ized ethylene anionic percarbonate Name water ether surfactant (EHP) Percentage (%) 81.36 0.24 0.20 18.20

(249) The formula of the terminator:

(250) TABLE-US-00046 Deionized Diethylhydroxylamine Name water (DEHA) Percentage (%) 50 50

(251) The formula of the neutralizer:

(252) TABLE-US-00047 Deionized Sodium Name water hydroxide Percentage (%) 65 35

(253) The formula of the defoamer:

(254) TABLE-US-00048 Deionized Name water Silane Percentage (%) 65 35

(255) The balance was water.

(256) The method of preparing the copolymerized REPVDC alloy solid resin is described as follows:

(257) 1) A No. 7 reactor was sealed, vacuumized and nitrogen was charged thrice to wash the reactor. The reactor was vacuumized again to −0.080-0.100 megapascal.

(258) 2) Hot deionized water was added to the reactor where the water accounted for 30% of the total volume of the reactor. The reaction standard temperature was set at 60±−0.2° C. The deionized water was stirred at 500-800 rpm at a constant temperature.

(259) 3) When the temperature rose to 50° C., the emulsified monomers were added to the reactor where the emulsified monomers accounted for 50% of the total volume of the reactor.

(260) 4) When the temperature rose to 55° C., the initiator mixture was added to the reactor where the initiator mixture accounted for 7% of the total volume of the reactor. The addition process was performed at the average speed within 4-6 hours.

(261) 5) When the pressure decreased to ≤0.050 megapascal, the conversion rate of REPVDC resin was ≥85%, and the terminator accounting for 2% of the total volume of the reactor was added. 5 minutes later, the discharge valve on the bottom of No. 7 reactor was opened. The discharge valve was connected to a No. 8 reactor. The No. 8 reactor was vacuumized, and the materials then flowed to the No. 8 reactor, and stirred at 500-800 rpm. The valve of the No. 7 reactor was closed, and then 30% of deionized water and 50% of emulsified monomers were added. The above operations were repeated.

(262) 6) The No. 8 reactor was heated to 60° C., the nitrogen valve and vacuum pump switch of the reactor were opened to discharge the unreacted monomers. The unreacted monomers were recycled and stored through a condenser and reused with the new monomer at the ratio of 1:10 in the next cycle.

(263) 7) 1-3 hours later, 0.13 wt. % of the neutralizer was added to the No. 8 reactor until the pH value was 6-7. Thereafter, 0.1 wt. % (total weight of the materials) of the defoamer was dropwise added, stirred for 3-5 min until no foam produced. The reactor was cooled and the product was collected.

(264) 8) The product was semi-dried by a centrifuge, washed using deionized water and rinse materials, dehydrated by a centrifuge, dried by a drier, to yield the REPVDC alloy solid resin.

(265) The prepared REPVDC alloy solid resin has good barrier, general strength, suitable for injection molding of thin, less stressed packaging containers. The molecular weight of the resin obtained by the preparation process is small.

Example 20

(266) The formula of the copolymerized REPVDC alloy solid emulsion is described as follows.

(267) The formula of the monomer mixture:

(268) TABLE-US-00049 Functional Isooctyl Vinylidene Acrylic Name monomer acrylate Acrylonitrile chloride phosphate Percentage 8.20 4.80 2.00 65.74 1.80 (%)

(269) The formula of the dispersant mixture:

(270) TABLE-US-00050 Non-ionic fatty acid Silicone β- Deionized polyoxyethylene anionic Polyvinyl Mercapto- Name water ether surfactant alcohol Ammonia ethanol Percentage 14.70 0.12 0.10 1.43 1.10 0.006% (%)

(271) The formula of the initiator mixture:

(272) TABLE-US-00051 Non-ionic fatty acid Deion- polyoxy- Silicone Diisopropyl ized ethylene anionic perdicarbonate Name water ether surfactant (IPP) Percentage (%) 82.06 0.24 0.20 17.5

(273) The formula of the terminator:

(274) TABLE-US-00052 Deionized Diethylhydroxylamine Name water (DEHA) Percentage (%) 50 50

(275) The formula of the neutralizer:

(276) TABLE-US-00053 Deionized Sodium Name water hydroxide Percentage (%) 65 35

(277) The formula of the defoamer:

(278) TABLE-US-00054 Deionized Name water Silane Percentage (%) 65 35

(279) The balance was water.

(280) The method of preparing the copolymerized REPVDC alloy solid resin is described as follows:

(281) 1) A No. 7 reactor was sealed, vacuumized and nitrogen was charged thrice to wash the reactor. The reactor was vacuumized again to −0.080-0.100 megapascal.

(282) 2) Hot deionized water was added to the reactor where the water accounted for 30% of the total volume of the reactor. The reaction standard temperature was set at 55±0.2° C. The deionized water was stirred at 500-800 rpm at a constant temperature.

(283) 3) When the temperature rose to 45° C., the emulsified monomers were added to the reactor where the emulsified monomers accounted for 50% of the total volume of the reactor.

(284) 4) When the temperature rose to 50° C., the initiator mixture was added to the reactor where the initiator mixture accounted for 7% of the total volume of the reactor. The addition process was performed at the average speed within 4-6 hours.

(285) 5) When the pressure decreased to ≤0.050 megapascal, the conversion rate of REPVDC resin was ≥85%, and the terminator accounting for 2% of the total volume of the reactor was added. 5 minutes later, the discharge valve on the bottom of No. 7 reactor was opened. The discharge valve was connected to a No. 8 reactor. The No. 8 reactor was vacuumized, and the materials then flowed to the No. 8 reactor, and stirred at 500-800 rpm. The valve of the No. 7 reactor was closed, and then 30% of deionized water and 50% of emulsified monomers were added. The above operations were repeated.

(286) 6) The No. 8 reactor was heated to 60° C., the nitrogen valve and vacuum pump switch of the reactor were opened to discharge the unreacted monomers. The unreacted monomers were recycled and stored through a condenser and reused with the new monomer at the ratio of 1:10 in the next cycle.

(287) 7) 1-3 hours later, 0.13 wt. % of the neutralizer was added to the No. 8 reactor until the pH value was 6-7. Thereafter, 0.1 wt. % (total weight of the materials) of the defoamer was dropwise added, stirred for 3-5 min until no foam produced. The reactor was cooled and the product was collected.

(288) 8) The product was semi-dried by a centrifuge, washed using deionized water and rinse materials, dehydrated by a centrifuge, dried by a drier, to yield the REPVDC alloy solid resin.

(289) The prepared REPVDC alloy solid resin has good barrier, general strength, suitable for injection molding of thin, more stressed packaging containers. The molecular weight of the resin obtained by the preparation process is moderate.

Example 21

(290) The formula of the copolymerized REPVDC alloy solid emulsion is described as follows.

(291) The formula of the monomer mixture:

(292) TABLE-US-00055 Functional Isooctyl Vinylidene Acrylic Name monomer acrylate Acrylonitrile chloride phosphate Percentage 10.00 5.00 2.00 63.51 1.41 (%)

(293) The formula of the dispersant mixture:

(294) TABLE-US-00056 Non-ionic fatty acid Fluorinate β- Deionized polyoxyethylene anionic Polyvinyl Ammonium Mercapto- Name water ether surfactant alcohol bicarbonate ethanol Percentage 16.00 0.15 0.12 0.80 1.00 0.008% (%)

(295) The formula of the initiator mixture:

(296) TABLE-US-00057 Non-ionic fatty acid Di-2- Deion- polyoxy- Fluorinated ethylhexyl ized ethylene anionic percarbonate Name water ether surfactant (EHP) Percentage (%) 84.06 0.24 0.20 15.5

(297) The formula of the terminator:

(298) TABLE-US-00058 Deionized Diethylhydroxylamine Name water (DEHA) Percentage (%) 50 50

(299) The formula of the neutralizer:

(300) TABLE-US-00059 Deionized Sodium Name water hydroxide Percentage (%) 65 35

(301) The formula of the defoamer:

(302) TABLE-US-00060 Deionized Name water Silane Percentage (%) 65 35

(303) The balance was water.

(304) The method of preparing the copolymerized REPVDC alloy solid resin is described as follows:

(305) 1) A No. 7 reactor was sealed, vacuumized and nitrogen was charged thrice to wash the reactor. The reactor was vacuumized again to −0.080-0.100 megapascal.

(306) 2) Hot deionized water was added to the reactor where the water accounted for 30% of the total volume of the reactor. The reaction standard temperature was set at 50±0.2° C. The deionized water was stirred at 500-800 rpm at a constant temperature.

(307) 3) When the temperature rose to 40° C., the emulsified monomers were added to the reactor where the emulsified monomers accounted for 50% of the total volume of the reactor.

(308) 4) When the temperature rose to 45° C., the initiator mixture was added to the reactor where the initiator mixture accounted for 7% of the total volume of the reactor. The addition process was performed at the average speed within 4-6 hours.

(309) 5) When the pressure decreased to ≤0.050 megapascal, the conversion rate of REPVDC resin was ≥85%, and the terminator accounting for 2% of the total volume of the reactor was added. 5 minutes later, the discharge valve on the bottom of No. 7 reactor was opened. The discharge valve was connected to a No. 8 reactor. The No. 8 reactor was vacuumized, and the materials then flowed to the No. 8 reactor, and stirred at 500-800 rpm. The valve of the No. 7 reactor was closed, and then 30% of deionized water and 50% of emulsified monomers were added. The above operations were repeated.

(310) 6) The No. 8 reactor was heated to 60° C., the nitrogen valve and vacuum pump switch of the reactor were opened to discharge the unreacted monomers. The unreacted monomers were recycled and stored through a condenser and reused with the new monomer at the ratio of 1:10 in the next cycle.

(311) 7) 1-3 hours later, 1.5 wt. % of the neutralizer was added to the No. 8 reactor until the pH value was 6-7. Thereafter, 0.1 wt. % (total weight of the materials) of the defoamer was dropwise added, stirred for 3-5 min until no foam produced. The reactor was cooled and the product was collected.

(312) 8) The product was semi-dried by a centrifuge, washed using deionized water and rinse materials, dehydrated by a centrifuge, dried by a drier, to yield the REPVDC alloy solid resin.

(313) The prepared REPVDC alloy solid resin has good barrier, general strength, suitable for blown film formation. The molecular weight of the resin obtained by the preparation process is large.

(314) The REPVDC alloy solid resins obtained in Examples 19-21 have the parameters as follows:

(315) TABLE-US-00061 Example Example Example Executive Term 19 20 21 Standard Tensile strength/MPa, 156/178 172/220 190/252 BB/0012- vertical/horizontal 2008 (5.6) Elongation at break/%, 151/110 189/136 256/184 vertical/horizontal Tear resistance/N, 1.02/1.06 1.34/1.29 1.67/1.53 vertical/horizontal Heat shrinkable rate/%, −15/−14 −18/−19 −22/−20 vertical/horizontal Water vapor transmission 0.4 0.5 0.8 rate/g/(m.sup.2, 24 H) Oxygen permeability/ 4.1 4.7 5.4 cm.sup.3/(m.sup.2/24 h .Math. 0.1 MPa) Thermal stability 150° C. 150° C. 150° C. ISO 182- 1: 1990

(316) It will be obvious to those skilled in the art that changes and modifications may be made, and therefore, the aim in the appended claims is to cover all such changes and modifications.