Eco-friendly flooring and method for manufacturing same

Abstract

Described herein is flooring formed of an eco-friendly material, where the flooring has excellent heat resistance, durability, abrasion resistance and dimensional stability, and is formed of a non-PVC material and thus is recyclable via an extrusion processing at the time of disposal after use. Specifically, eco-friendly flooring is described in which a coating layer, an overlayer having ionomers, a printing layer, at least one middle layer, and at least one underlayer are laminated in order, where the overlayer of the flooring has ionomers, at least one of the middle layer and the underlayer has a thermoplastic polyolefin-based resin, a styrene-based resin, oil, and a filler, the thermoplastic polyolefin-based resin is contained in an amount of 50 to 150 parts by weight with respect to 100 parts by weight of the styrene-based resin, and the styrene-based resin may contain 25 to 45% styrene.

Claims

1. An environmentally-friendly flooring comprising: a coating layer; an upper layer including an ionomer; a printing layer; at least one intermediate layer; and at least one underlayer, which are sequentially laminated, at least one of the intermediate layer and the underlayer includes a thermoplastic polyolefin-based resin, a styrene-based resin, oil, and a filler, the thermoplastic polyolefin-based resin is included in an amount of 50 parts by weight to 150 parts by weight with respect to 100 parts by weight of the styrene-based resin, and the styrene-based resin includes styrene in an amount of 25% to 45, wherein at least one of the intermediate layers and the underlayer includes 10 parts by weight to 50 parts by weight of thermoplastic vulcanizate (TPV) with respect to 100 parts by weight of the styrene-based resin, wherein a shrinkage rate of the upper layer is in a range of 0.7% to 0.9% in a flow direction and in a range of 0.2% to 0.4% in a vertical direction.

2. The environmentally-friendly flooring of claim 1, wherein the styrene-based resin includes the styrene in the amount of 25% to 35%.

3. The environmentally-friendly flooring of claim 1, wherein at least one of the intermediate layer and the underlayer additionally includes 10 parts by weight to 50 parts by weight of at least one engineering plastic resin with respect to 100 parts by weight of the styrene-based resin, wherein the at least one engineering plastic resin is selected from polyethersulfone (PES), polyether ether sulfone (PEES), polyetherimide (PEI), polyphenylene oxide (PPO), polyacetal (POM), polyamide (PA), polycarbonate (PC), polysulfone (PSF), polyphenylene sulfide (PPS), polyamideimide (PAI), polyacrylate (PAR), polyketone (PK), polyethylene terephthalate (PET), polybutylene terephtalate (PBT), nylon (NA), polyimide (PI), polyetheretherketone (PEEK), and a liquid crystal polymer (LCP).

4. The environmentally-friendly flooring of claim 1, wherein at least one of the intermediate layer and the underlayer includes 500 parts by weight to 1,500 parts by weight of the filler and 100 parts by weight to 300 parts by weight of the oil with respect to 100 parts by weight of the styrene-based resin.

5. The environmentally-friendly flooring of claim 1, wherein the styrene-based resin includes at least one selected from poly(styrene-b-butadiene-b-styrene) (SBS), poly(styrene-b-isoprene-styrene) (SIS), poly(styrene-butylene-b-butadiene-b-styrene) (SEBS), and poly(styrene-b-ethylene-b-propylene-b-styrene) (SEPS).

6. The environmentally-friendly flooring of claim 1, wherein the thermoplastic polyolefin-based resin includes one selected from polyethylene, polypropylene, MAH-PP (Maleic Anhydride-PP), LLDPE (Linear Low-Density Polyethylene), HDPE (High-Density Polyethylene), and mixtures thereof.

7. The environmentally-friendly flooring of claim 1, wherein one or more dimensional stability layers are additionally provided between the intermediate layer and the underlayer and/or below the underlayer.

8. The environmentally-friendly flooring of claim 1, wherein one or more primer layers are provided between the coating layer, the upper layer, the printing layer, the intermediate layer, and the underlayer.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a cross-sectional view illustrating a first aspect of environmentally-friendly flooring of the present invention.

(2) FIG. 2 is a cross-sectional view illustrating a second aspect of environmentally-friendly flooring of the present invention.

(3) FIG. 3a is a cross-sectional view illustrating a third aspect of environmentally-friendly flooring of the present invention.

(4) FIG. 3b is another cross-sectional view illustrating a third aspect of environmentally-friendly flooring of the present invention.

BEST MODE OF THE INVENTION

(5) Hereinafter, the present invention will be described in detail. Hereinafter, a configuration of the present invention will be described in detail with reference to the accompanying drawings. The following drawings to be described below are provided by way of example so that the idea of the present invention can be sufficiently transferred to those skilled in the art to which the present invention pertains. Therefore, the present invention may be implemented in many different forms, without being limited to the drawings to be described below. Here, unless technical and scientific terms used herein are defined otherwise, they have meanings generally understood by those skilled in the art to which the present invention pertains. Description of known functions and components that may unnecessarily obscure the gist of the present invention will be omitted from the following description and the accompanying drawings.

(6) Novel environmentally-friendly flooring according to the present invention has high heat resistance, durability, abrasion resistance, and dimensional stability and is made of an environmentally-friendly material as a non-PVC material that is recyclable through extruding when being discarded after use

(7) An embodiment of the present invention relates to environmentally-friendly flooring including a coating layer, an upper layer including an ionomer, a printing layer, at least one intermediate layer, and at least one underlayer, which are sequentially laminated. The upper layer of the flooring may include the ionomer. The at least one of the intermediate layer and the underlayer may include a thermoplastic polyolefin-based resin, oil, and a filler. The thermoplastic polyolefin-based resin may be included in an amount of 50 parts by weight to 150 parts by weight with respect to 100 parts by weight of a styrene-based resin. The styrene-based resin may include styrene in an amount of 25% to 45%.

(8) FIG. 1 illustrates a first aspect of the present invention, which sequentially includes the coating layer, the upper layer, the printing layer, the intermediate layer, and the underlayer.

(9) The intermediate layer and/or the underlayer of the flooring according to the present invention include the thermoplastic polyolefin-based resin. The thermoplastic polyolefin-based resin may include various known types. Desirably, the thermoplastic polyolefin-based resin may include a polyethylene PE, polypropylene (PP), or rubber elastomer resin group, but the present invention is not limited thereto. For example, the thermoplastic polyolefin-based resin may include at least one resin selected LDPE, EVA, HDPE, LLDPE UHMWPE, homo PP, random PP, Ter PP, block PP, EPR, EPDM, and POE. Desirably, the thermoplastic polyolefin-based resin may include one selected from PE, PP, MAH-PP, LLDPE, HDPE, and mixtures thereof.

(10) The intermediate layer and/or the underlayer of the flooring according to the present invention include a styrene polymer and a styrene-based resin including styrene as a main component. The styrene-based resin may include an ethylene/styrene copolymer. In an example, the styrene-based resin may include resins such as poly(styrene-b-butadiene-b-styrene) (SBS), poly(styrene-b-isoprene-styrene) (SIS), poly(styrene-butylene-b-butadiene-b-styrene) (SEBS) (poly(styrene-b-ethylene-b-butadiene-b-styrene) (SEBS)), and poly(styrene-b-ethylene-b-propylene-b-styrene) (SEPS).

(11) ##STR00001##

(12) In the styrene-based resin of the present invention, a content of the styrene is desirably in a range of 25% to 45% and is more desirably in a range of 23% to 35%. When the content of the styrene exceeds 45% in the styrene-based resin, there is a problem in compatibility with a polyolefin-based resin. When the content of styrene is less than 25%, a shrinkage rate of the intermediate layer and/or the underlayer is considerably increased, and a compression set is considerably increased. Thus, durability and dimensional stability are considerably degraded. On the other hand, when the content of the styrene is satisfied, dimension stability of the flooring is secured, and thus, a distortion phenomenon and a crack phenomenon of the flooring are prevented.

(13) According to the present invention, in order to improve abrasion resistance, heat resistance, durability, and dimensional stability of the flooring, at least one intermediate layer and/or at least one intermediate layer include oil and a filler. During a use period of the flooring, a floor is warped by external shock, external pressure, and/or an external temperature, and particularly, the floor is warped due to a shrinkage rate difference or a distortion degree difference between layers caused by external nonuniform pressure or an external temperature being applied on the upper layer.

(14) Specific kinds of the filler usable in the present invention are not particularly limited, and the filler may include at least one selected from inorganic-based fillers such as calcium carbonate, talc, loess, silica, and alumina; and organic-based fillers such as wood-based fillers (for example, a wood powder and a wood chip), cork, kenaf, and pulp. The filler of the present invention may have high compatibility with a resin, may exhibit smooth workability during melting, may have high affinity with a plasticizer, and may suppress elution of the plasticizer.

(15) The filler may be contained in an amount of 500 parts by weight to 1,500 parts by weight and be desirably adjusted in a range of 1,100 parts by weight to 1,300 parts by weight, with respect to 00 parts by weight of the styrene-based resin. When the numerical range is satisfied, a shrinkage rate of the flooring is decreased to increase dimensional stability. On the other hand, when the amount of the filler applied in the present invention is too low, a reinforcing effect or the like may be insignificant. On the contrary, when the amount of the filler is excessively increased, a bonding force of other components such as a resin may be decreased to decrease workability.

(16) The oil is not limited as long as the oil is process oil and includes paraffinic-based, naphthenic-based, or aromatic-based process oil. Desirably, the paraffinic process oil may be used. Examples of the process oil include P-1, P-2, P-3, P-4, P-5, P-6, N-1, N-2, and N-3. The oil may be included in an amount of 100 parts by weight to 300 parts by weight and be desirably adjusted in a range of 150 parts by weight to 250 parts by weight with respect to 100 parts by weight of the styrene-based resin. When a content of the oil is high, a filler filling rate in the thermoplastic polyolefin-based resin may be increased. On the contrary, when the content of the oil is too high, oil leaks from a surface of the intermediate layer and/or the underlayer as time elapses.

(17) Engineering plastic is high performance plastic suitable for structural and mechanical components and is used as a resin aimed to mainly replace a metal or widely used in vehicle, machine, electric, and electronic components. The engineering plastic is defined as plastic that has a tensile strength of 500 Kgf/cm.sup.2 or more, a flexural modulus of Kgf/cm.sup.2 or more, and a heat resistance of 100° C. or more. At least one of the intermediate layer and the underlayer in the present invention may additionally include at least one engineering plastic resin in an amount of 10 parts by weight to 100 parts by weight, and desirably, 10 parts by weight to 40 parts by weight with respect to 100 parts by weight of the styrene-based resin, wherein the at least one engineering plastic resin is selected from polyethersulfone (PES), polyether ether sulfone (PEES), polyetherimide (PEI), polyphenylene oxide (PPO), polyacetal (POM), polyamide (PA), polycarbonate (PC), polysulfone (PSF), polyphenylene sulfide (PPS), polyamideimide (PAI), polyacrylate (PAR), polyketone (PK), polyethylene terephthalate (PET), polybutylene terephtalate (PBT), nylon (NA), polyimide (PI), polyetheretherketone (PEEK), and a liquid crystal polymer (LCP). The PPO may be used as the engineering plastic. When the above range is satisfied, durability, abrasion resistance, and heat resistance of the flooring are considerably improved. When the engineering plastic is added, a content ratio of the engineering plastic to an olefin-based resin may be in a range of 30:1 to 3:1, and desirably, a range of 13:1 to 13:4.

(18) The intermediate layer and/or the underlayer of the flooring according to the present invention nay additionally include a dynamically crosslinked thermoplastic elastomer composition (thermoplastic vulcanizate (TPV)). Examples of a crosslinked thermoplastic elastomer include ethylene propylene rubber (EPDM), nitrile butadiene rubber (NBR), natural rubber (NR), and butyl rubber. The TPV may be included in an amount of 10 parts to 100 parts by weight, and desirably, 10 parts to 50 parts by weight with respect to 100 parts by weight of the styrene-based resin. When the numerical range is satisfied, a shrinkage rate of the flooring is decreased to increase dimensional stability.

(19) In the present invention, the flooring may be mixed with typical additives such as an ultraviolet screening agent, an antioxidant, an antibacterial agent, an antifungal agent, a deodorant, an air freshener, and a flame retardant within a range in which the object of the present invention is not impaired.

(20) The flooring of the present invention may additionally include one or more dimensional stability layers between the intermediate layer and the underlayer and/or below the underlayer. FIGS. 2A to 2C illustrate that the flooring additionally includes one or more dimensional stability layers between the intermediate layer and the underlayer and/or below the underlayer. The dimensional stability layer may be made of at least one nonwoven fabric selected from the group consisting of a glass fiber, a carbon fiber, a polyester fiber, a polyamide fiber, a polyurethane fiber, an acrylic fiber, a polyolefin fiber, and a cellulose fiber.

(21) Another embodiment of the present invention provides a method of manufacturing environmentally-friendly flooring, the method including (a) providing an upper layer including an ionomer and a printing layer; (b) co-extruding the upper layer and the printing layer to mold a first sheet; (c) preparing a resin composition including 50 parts by weight to 150 parts by weight of a thermoplastic polyolefin-based resin with respect to 100 parts by weight of a styrene-based resin and manufacturing a second sheet and a third sheet including an intermediate layer and an underlayer pressed from the resin composition; and (d) sequentially laminating and pressing the first sheet, the second sheet, and the third sheet manufactured in (a) and (b). In an embodiment of the invention, in the method, one or more second and/or third sheets may be manufactured and laminated in a random order. The method may additionally include laminating one or more dimensional stability layers between the intermediate layer and the underlayer or below the underlayer.

(22) The upper layer according to the present invention includes the ionomer. An ionomer may be prepared by neutralizing an ethylene acid copolymer with one or more metal ions through a method known in the art. The ionomer may be a mixture of an ionomer and about 1 part by weight to about 50 parts by weight of an ethylene alkyl(meth)acrylate copolymer. Examples of such alkyl(meth)acrylate include one selected from methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, glycidyl acrylate, glycidyl methacrylate, one or more of above-described acrylates, and combinations of two or more thereof.

(23) The ethylene acid copolymer is a polymer that may include repeat units derived from ethylene and about 1 wt % to about 50 wt %, or about 5 wt % to about 40 wt %, or 10 wt % to 25 wt % of a comonomer such as an acrylic acid, a methacrylic acid, an ethacrylic acid, or combinations of two or more thereof, with respect to the total weight of an ethylene copolymer. The ionomer is well known in the art, and detailed descriptions thereof will be omitted for the interest of brevity

(24) A transparent coating layer is laminated on the upper layer. In an embodiment, a ultraviolet (UV)-curable urethane acrylic-based resin may be applied on the upper layer, and then, UV light may be irradiated to form the coating layer, wherein the upper layer is an uppermost layer of a sheet in which the upper layer including the ionomer, the printing layer, the intermediate layer, and the underlayer are sequentially laminated. The coating layer may be made of a polyurethane-based or polyacrylic-based resin. The coating layer may additionally include typical additives such as an ultraviolet screening agent, an antioxidant, an antibacterial agent, an antifungal agent, a deodorant, an air freshener, and a flame retardant.

(25) In an embodiment of the present invention, one or more primer layers may be disposed between the coating layer, the upper layer, the printing layer, the intermediate layer, and the underlayer. For example, in order to improve an adhesive force between the upper layer and the printing layer, corona discharge treatment may be performed or a primer layer may be formed on a surface of an olefin-based resin sheet. FIGS. 3A and 3B illustrate that one or more primer layers are additionally disposed between one or more layers of the coating layer, the upper layer, the printing layer, the intermediate layer, and the underlayer. The content and thickness of the primer layer may be optionally applied.

(26) In an embodiment of the present invention, the first to third sheets may be pressed through a press process. In this case, a natural texture of the flooring may be revived, and an adhesive force between layers may also be improved. The press process is performed under appropriate pressure, time, and temperature according to the thickness and composition of the sheet. The press process may be performed twice or more at a pressure of 40 kgf/cm.sup.2 to 50 kgf/cm.sup.2 at a temperature of 160° C. and 170° C. for 300 seconds to 500 seconds, and desirably, for 360 seconds. When pressure is lower than the appropriate pressure, attaching between layers and molding are incomplete. When pressure is higher than the appropriate pressure, the thickness of the sheet is decreased. Thus, the upper layer is damaged and broken, which makes it difficult to implement an appropriate product thickness (3 mm to 5 mm). In addition, when pressing is not performed for an appropriate time, both ends are not attached. When a temperature is not within an appropriate temperature range, an adhesive force between the layers is weakened, resulting in deformation of the upper layer and the printing layer. The press process may be performed three or more times. When the press process is performed only once, a probability of bubble generation is high, which leads to adhesion failure.

(27) Hereinafter, exemplary examples of the present invention will be described for promoting an understanding of the invention. However, the following examples are provided only for understanding the present invention more easily, but the content of the present invention is not limited thereby. Various other modifications and variations may be possible.

MODES OF THE INVENTION

Preparation Example 1: Preparation of Resin Composition of Intermediate Layer A and Underlayer

(28) In order to obtain an intermediate layer A, resin compositions shown in Table 1 below were prepared. A content of styrene in styrene-based resins of Examples 1 to 4 was in a range of 25% to 45%, and in the case of Comparative Examples 1 and 2, resin compositions were prepared such that a content of styrene deviates a range of the styrene.

(29) TABLE-US-00001 TABLE 1 styrene-based resin filler* SEBS polyolefin-based resin* EP* oil* calcium (styrene, %) PP MAH-PP LLDPE HDPE TPV* PPO oil carbonate Example 1 100 (29%) 40 30 30 30 — — 250 1,300 Example 2 100 (31%) 40 30 30 30 — — 250 1,300 Example 3 100 (33%) 40 30 30 30 — — 250 1,300 Example 4 100 (41%) 40 30 30 30 — — 250 1,300 Comparative 100 (13%) 40 30 30 30 — — 250 1,300 Example 1 Comparative 100 (58%) 40 30 30 30 — — 250 1,300 Example 2 *unit: parts by weight with respect to 100 parts by weight of styrene-based resin

Manufacture Example 2: Formation of Intermediate Layer B

(30) In order to obtain an intermediate layer B, resin compositions shown in Table 2 below were prepared. A composition of the intermediate layer B is a composition in which TPV is further added to a composition of the intermediate layer A.

(31) TABLE-US-00002 TABLE 2 styrene-based resin filler* SEBS polyolefin-based resin* EP* oil* calcium (Styrene, %) PP MAH-PP LLDPE HDPE TPV* PPO oil carbonate Example 5 100(33%) 40 30 30 30 10 — 250 1,300 Example 6 100(33%) 40 30 30 30 15 — 250 1,300 Example 7 100(33%) 40 30 30 30 20 — 250 1,300 Example 8 100(33%) 40 30 30 30 30 — 250 1,300 *unit: parts by weight with respect to 100 parts by weight of styrene-based resin

Manufacture Example 3: Formation of Intermediate Layer C

(32) In order to obtain an intermediate layer C, resin compositions shown in Table 3 below were prepared. A composition of the intermediate layer C is a composition in which PPO as engineering plastic is further added to the composition of the intermediate layer B.

(33) TABLE-US-00003 TABLE 3 styrene-based resin filler* SEBS polyolefin-based resin* TPV* EP* oil* calcium (Styrene, %) PP MAH-PP LLDPE HDPE — PPO oil carbonate Example 9 100(33%) 40 30 30 30 20 10 250 1,300 Example 100(33%) 40 30 30 30 20 20 250 1,300 10 Example 100(33%) 40 30 30 30 20 30 250 1,300 11 Example 100(33%) 40 30 30 30 20 40 250 1,300 12 Example 100(33%) 40 30 30 30 20 50 250 1,300 13 Example 100(33%) 40 30 30 40 20 40 250 1,300 14 Example 100(33%) 40 30 30 45 20 45 250 1,300 15 1) SEBS: styrene-ethylene-butylene-styrene copolymer manufactured by KRATON 2) PP: polypropylene manufactured by LG Chem 3) MAH-PP: maleic anhydride grafted polypropylene manufactured by Lotte Chemical 4) LLDPE: linear low density polyethene manufactured by LG Chem 5) HDPE: high density polyethylene manufactured by LG Chem 6) TPV: dynamic crosslinkable thermoplastic Elastomer manufactured by ExxonMobil 7) EP: engineering plastic manufactured by SABIC, polyphenylene oxide (PPO) 8) oil: process oil manufactured by MICHANG Petroleum Industry 9) filler manufactured by Omya Korea, calcium carbonate

Experimental Example 1: Evaluation of Physical Properties of Intermediate Layer

(34) The intermediate layers A to C prepared in Preparation Example 1 were used to form sheets, and then, physical properties thereof were evaluated by the following method and shown in Tables 4 to 6. A target layer is a layer attached to an intermediate layer like an upper layer or an underlayer when flooring is manufactured. In the present experiment, the target layer is a sheet made of a composition including an ethylene-acrylic acid copolymer (EAA) as a main component.

(35) Evaluation Method

(36) 1) shrinkage rate: after the formed sheet was left at room temperature for 24 hours, a flow direction of a resin composition and a change rate of a length of the resin composition in a vertical direction was measured.

(37) 2) change rate of heated length: after the formed sheet was left at a temperature 80° C. for 6 hours and then cooled at room temperature for 1 hour, an average value of three change rates was measured.

(38) 3) heating loss rate: after the formed sheet was left at 100° C. for 6 hours and cooled at room temperature for 1 hour, and then, a heating loss rate was measured.

(39) 4) compression set (C/S): After the formed sheet was left at a temperature of 45° C. for 22 hours and cooled at room temperature for 1 hour, and then, a change rate of a thickness was measured.

(40) 5) specific gravity: specific gravity was measured using a specific gravity meter (MD-300S manufactured by Alfa Mirage Co. LTD)

(41) TABLE-US-00004 TABLE 4 shrinkage rate [%] C/S content of shrinkage shrinkage physical styrene flow rate vertical rate specific gravity results [%] direction difference direction difference [%] [—] Target — 0.82 0.24 — 0.9 Example 1 29 0.89 +0.07 0.39 +0.15 67 1.72 Example 2 31 0.73 −0.09 0.34 +0.10 58 1.72 Example 3 33 0.77 −0.05 0.22 −0.02 68 1.72 Comparative 13 0.94 +0.12 0.41 +0.17 56 1.72 Example 1 Comparative 58 0.63 −0.19 0.46 +0.22 73 1.72 Example 2

(42) According to Table 4, in the case of Example 3 in which a content of styrene in a styrene-based resin was 33%, a shrinkage rate was smaller in both a flow direction and a vertical direction as compared with Comparative Example 2. On the other hand, in the case of Comparative Examples 1 and 2, since a shrinkage rate difference in with respect to the target layer (upper layer) is very large, it can be seen that there is a high possibility that a distortion phenomenon occurs in the sheet.

(43) In the case of PVC flooring, since constituent materials of respective layers are mostly the same PVC, a shrinkage rate of a sheet is relatively easy controlled. When materials of the respective layers are different, a floor warpage phenomenon is likely to occur to a shrinkage rate difference. As described above, the control of a shrinkage rate between layers is important for dimensional stability and durability of flooring. In the present invention, the dimensional stability and durability of the flooring are secured by easily controlling a shrinkage rate.

(44) TABLE-US-00005 TABLE 5 content of shrinkage rate [%] specific tensile physical styrene flow vertical C/S gravity strength elongation results [%] direction direction [%] [—] [MPa] [%] Target — 0.82 0.24 — 0.9 — — Example 5 33 0.8 0.22 72 1.72 63 102 Example 6 33 0.8 0.23 70 1.73 60 121 Example 7 33 0.81 0.23 67 1.72 58 120 change rate sheet performance content of of heated heating oil physical styrene length loss rate wettability flatness performance tactility results [%] [%] [%] [—] [—] (90° C.) (rough) Target [—] 0.25 or less 0.5 or less ∘ ∘ ∘ ∘ Example 5 33 0.14 0.2 ∘ ∘ ∘ ∘ Example 6 33 0.13 0.17 ∘ ∘ ∘ ∘ Example 7 33 0.13 0.18 ∘ ∘ ∘ ∘ (∘: excellent, Δ: normal, X: defective)

(45) According to Table 5, Example 7 had excellent wettability, flatness, and sheet performance.

(46) TABLE-US-00006 TABLE 6 content of shrinkage rate [%] specific tensile physical styrene flow vertical C/S gravity strength elongation results [%] direction direction [%] [—] [MPa] [%] Target — 0.82 0.24 — 0.9 — — Example 9 33 0.79 0.22 60 1.72 64 144 Example 10 33 0.79 0.21 48 1.72 66 136 Example 11 33 0.77 0.2 28 1.72 67 128 Example 12 33 0.77 0.2 13 1.72 69 114 Example 13 33 0.76 0.19 12 1.72 70 128 change rate sheet performance of heated heating oil physical length loss rate wettability workability performance tactility results [%] [%] [—] [—] (90° C.) (rough) Target 0.25 or less 0.5 or less ∘ ∘ ∘ ∘ Example 9 0.18 0.17 ∘ ∘ ∘ ∘ Example 10 0.18 0.18 ∘ ∘ ∘ ∘ Example 11 0.17 0.19 ∘ ∘ ∘ ∘ Example 12 0.16 0.18 ∘ ∘ ∘ ∘ Example 13 0.16 0.18 Δ Δ ∘ Δ

(47) According to Table 6, all of Examples 9 to 12 had excellent wettability, flatness, and sheet performance.

Experimental Example 2: Manufacture and Evaluation of Physical Properties of Flooring

(48) (1) An upper layer including an ionomer (surlyn) and an olefin-based printing layer film were sheet-molded using an extruder, the compositions of the intermediate layers of Examples 12, 14, and 5, and Comparative Example 5 were mixed using a Banbury mixer, and sheets were molded through a calendar process. An underlayer sheet including a composition according to Table 7 below was formed in the same manner as in an intermediate layer. Each layer was laminated through a press process, and an optimum molding cycle of the press process was performed in such a manner that high temperature pressing was performed twice at a temperature of 160° C. to 170° C. at a pressure of 40 kgf/cm.sup.2 for 300 seconds, and then, cooling was performed once. Then, a UV coating layer was applied on the upper layer.

(49) TABLE-US-00007 TABLE 7 styrene-based filler* resin Polyolefin-based resin* oil* calcium SEBS(Styrene, %) PP MAH-PP LLDPE HDPE POE oil carbonate underlayer 100(33%) 40 30 30 30 30 250 1500 *unit: parts by weight with respect to 100 parts by weight of styrene-based resin

(50) (2) Physical properties of the manufactured flooring were evaluated according to the following method.

(51) 1) change rate of heated length: after the manufactured flooring was left at a temperature 80° C. for 6 hours and then cooled at room temperature for 1 hour, an average value of three change rates was measured.

(52) 2) heating loss rate: after the manufactured flooring was left at 100° C. for 6 hours and cooled at room temperature for 1 hour, an average value of three change rates was measured

(53) 3) residual indentation modulus: after a load of 36.3 kgf is loaded on the manufactured flooring for 10 minutes and removed, a residual indentation modulus was measured after 60 minutes.

(54) TABLE-US-00008 TABLE 8 inden- inden- residual change tation tation inden- rate of heating amount amount tation heated loss physical (20° C.) (45° C.) modulus length rate results [mm] [mm] [mm] [%] [%] Target 0.25 or 1.20 or 8.0 or 0.25 or 0.5 or less less less less less Example 12 1.2 1.3 6 0.1 0.1 Example 14 0.3 0.4 7 0.1 0.2 Example 15 0.2 0.3 6 0.1 0.1

(55) As shown in Table 8, it could be confirmed that dimensional stability of the flooring of Comparative Example 5 was considerably lower as compared with Examples. In particular, Comparative Example 5 had a residual indentation modulus of 37% and thus was very vulnerable to load, but Examples had a higher elastic restoring force against load.

(56) TABLE-US-00009 Reference Numerals 1: coating layer 2: upper layer 3: printing layer 4: intermediate layer 5: underlayer 6: dimensional stability layer 7: primer layer