KR101569489B1 - menufacturing method of filling material for a green artificial grass - Google Patents
menufacturing method of filling material for a green artificial grass Download PDFInfo
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- KR101569489B1 KR101569489B1 KR1020150116599A KR20150116599A KR101569489B1 KR 101569489 B1 KR101569489 B1 KR 101569489B1 KR 1020150116599 A KR1020150116599 A KR 1020150116599A KR 20150116599 A KR20150116599 A KR 20150116599A KR 101569489 B1 KR101569489 B1 KR 101569489B1
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- 239000000463 material Substances 0.000 title claims description 15
- 238000000034 method Methods 0.000 title claims description 15
- 238000011049 filling Methods 0.000 title claims description 6
- 244000025254 Cannabis sativa Species 0.000 title description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 58
- 239000000377 silicon dioxide Substances 0.000 claims description 29
- -1 polypropylene Polymers 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 24
- 229910044991 metal oxide Inorganic materials 0.000 claims description 13
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 12
- 239000004743 Polypropylene Substances 0.000 claims description 12
- 229920001155 polypropylene Polymers 0.000 claims description 12
- 239000004698 Polyethylene Substances 0.000 claims description 11
- 229920000573 polyethylene Polymers 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 11
- 238000003756 stirring Methods 0.000 claims description 9
- 239000008199 coating composition Substances 0.000 claims description 8
- 239000005662 Paraffin oil Substances 0.000 claims description 7
- 150000004706 metal oxides Chemical class 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- 230000003078 antioxidant effect Effects 0.000 claims description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 238000005520 cutting process Methods 0.000 claims description 4
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 4
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 239000000326 ultraviolet stabilizing agent Substances 0.000 claims description 4
- 239000000440 bentonite Substances 0.000 claims description 3
- 229910000278 bentonite Inorganic materials 0.000 claims description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004927 clay Substances 0.000 claims description 3
- 229910052570 clay Inorganic materials 0.000 claims description 3
- 229910052732 germanium Inorganic materials 0.000 claims description 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 2
- 229960002447 thiram Drugs 0.000 claims description 2
- 239000000945 filler Substances 0.000 abstract description 25
- 238000004519 manufacturing process Methods 0.000 abstract description 11
- 230000000843 anti-fungal effect Effects 0.000 abstract description 6
- 229910001385 heavy metal Inorganic materials 0.000 abstract description 5
- 239000012855 volatile organic compound Substances 0.000 abstract description 5
- 230000005611 electricity Effects 0.000 abstract description 4
- 125000003367 polycyclic group Chemical group 0.000 abstract description 4
- 230000003068 static effect Effects 0.000 abstract description 4
- 229940121375 antifungal agent Drugs 0.000 abstract description 2
- 230000003020 moisturizing effect Effects 0.000 abstract description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910010413 TiO 2 Inorganic materials 0.000 description 6
- 229920001971 elastomer Polymers 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- DFWCPLGXFMSUCW-UHFFFAOYSA-N 3-(dimethylamino)propyl carbamimidothioate;hydron;dichloride Chemical compound Cl.Cl.CN(C)CCCSC(N)=N DFWCPLGXFMSUCW-UHFFFAOYSA-N 0.000 description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000004636 vulcanized rubber Substances 0.000 description 3
- 239000010920 waste tyre Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920005549 butyl rubber Polymers 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000011941 photocatalyst Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 230000035943 smell Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- MZZSDCJQCLYLLL-UHFFFAOYSA-N Secalonsaeure A Natural products COC(=O)C12OC3C(CC1=C(O)CC(C)C2O)C(=CC=C3c4ccc(O)c5C(=O)C6=C(O)CC(C)C(O)C6(Oc45)C(=O)OC)O MZZSDCJQCLYLLL-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000001699 photocatalysis Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
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Classifications
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- E—FIXED CONSTRUCTIONS
- E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
- E01C—CONSTRUCTION OF, OR SURFACES FOR, ROADS, SPORTS GROUNDS, OR THE LIKE; MACHINES OR AUXILIARY TOOLS FOR CONSTRUCTION OR REPAIR
- E01C13/00—Pavings or foundations specially adapted for playgrounds or sports grounds; Drainage, irrigation or heating of sports grounds
- E01C13/08—Surfaces simulating grass ; Grass-grown sports grounds
Landscapes
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Road Paving Structures (AREA)
Abstract
본 발명은 친환경 인조잔디용 충진재 제조방법에 관한 것으로서, 보다 구체적으로는 중금속, 다환 방향족 화화물 및 VOC를 함유하지 않으며, 보습력이 우수하고 마찰에 의한 정전기 발생이 적고, 미세 분말이 발생치 않으며, 항곰팡이성 및 탄성력등이 우수한 친환경 인조잔디용 충진재 제조방법에 관한 것이다.More particularly, the present invention relates to a method for producing a filler for environmentally friendly artificial turf, which does not contain heavy metals, polycyclic aromatics and VOCs, has excellent moisturizing power, generates little static electricity by friction, Antifungal and elasticity, and the like.
Description
본 발명은 친환경 인조잔디용 충진재 제조방법에 관한 것으로서, 보다 구체적으로는 중금속, 다환 방향족 화화물 및 VOC를 함유하지 않으며, 보습력이 우수하고 마찰에 의한 정전기 발생이 적고, 미세 분말이 발생치 않으며, 항곰팡이성 및 탄성력등이 우수한 친환경 인조잔디용 충진재 제조방법에 관한 것이다.
More particularly, the present invention relates to a method for producing a filler for environmentally friendly artificial turf, which does not contain heavy metals, polycyclic aromatics and VOCs, has excellent moisturizing power, generates little static electricity by friction, Antifungal and elasticity, and the like.
일반적인 인조잔디는 도 2에 도시된 바와 같이 지반(40) 상부에 골재로 이루어진 골재층(30)을 형성하고, 상기 골재층(30) 상부에 NR(Natural Rubber), SBR(StyreneButadiene Rubber), IIR(Isobutylene Isoprene Rubber), NBR(Nitrile Butadiene Rubber), EPDM(Ethylene Propylene Terpolymers), 우레탄의 가황고무 고무칩(21)과 폴리우레탄 수지 또는 에폭시 수지와 같은 수지계 접착제(22)가 혼합 조성된 탄성층(20)을 형성하며, 상기 탄성층(20)의 상부에 바닥매트(14)에 다수의 인조잔디파일(11)이 심어진 상태에서 인조잔디파일(11) 사이에 가황고무칩(12)과 규사(13)가 채워진 인조잔디층(10)을 형성하여 이루어진다.2, an
종래의 인조잔디 충진용 고무칩은 가황고무칩을 사용하거나 아니면 폐타이어로부터 얻어진 재생 고무칩을 주로 사용하기 때문에, 고무칩을 인조잔디에 충진하였을때 인조잔디에서 고무냄새가 심하게 나는 문제점이 발생하고 있었고, 더욱이 폐타이어 재생 고무칩을 사용할 경우에는 인조잔디에서 폐타이어 냄새가 나는 문제가 있다.Conventional rubber chips for artificial turf filling use a vulcanized rubber chip or a reclaimed rubber chip obtained from a waste tire. Therefore, when the rubber chips are filled in artificial turf, there arises a problem that the synthetic rubber smells badly on the artificial turf Further, when using a waste tire reclaimed rubber chip, there is a problem of smell of waste tire in artificial turf.
이러한 문제를 해결하기 위해 대한민국 등록특허 제10-1400101호에는 에스이비에스(SEBS)소재 23중량%, 이브이에이(EVA) 10중량%, 탄산칼슘 54중량%, 커피슬러지 3중량%, 콜크분말 3중량%, 스테아린산 1중량%, 왁스 0.5중량%, 백오일 5중량%, 안료 0.5중량%를 개량하여 준비하는 제 1 단계와; 준비된 재료를 혼합기에 넣고 혼합하되, 준비된 에스이비에스(SEBS)소재, 이브이에이(EVA), 개량된 탄산칼슘의 1/2, 커피슬러지, 콜크분말, 스테아린산, 왁스, 백오일, 안료를 혼합기에 투입한 후 약 15분동안 1차 혼합하고, 1차 혼합 후 나머지 탄산칼슘 1/2을 혼합기에 투입한 후 5분동안 2차 혼합하는 제 2 단계와;혼합된 재료를 압출기에 투입하여 압출시키되, 압출물은 외주연에 복수의 탄성날개부를 갖고, 탄성날개부의 내측으로 홀을 구비한 형상이 되도록 압출하는 제 3 단계와; 압출물을 물속에서 2.5mm의 크기로 절단하는 제 4 단계와; 절단된 고무칩을 탈수기에 넣고 탈수한 후 상온에서 냉각시키는 제 5 단계; 로 구성한 것을 특징으로 하는 인조잔디 충진용 에스이비에스 고무칩 제조방법이 개시되어 있다.In order to solve this problem, Korea Patent No. 10-1400101 discloses a process for producing a coke oven which comprises 23 wt% of SEBS material, 10 wt% of EVA, 54 wt% of calcium carbonate, 3 wt% of coffee sludge, By weight, 1% by weight of stearic acid, 0.5% by weight of wax, 5% by weight of white oil and 0.5% by weight of pigment. Add the prepared materials to the mixer and mix them into the mixer with prepared SEBS material, EVA (EVA), 1/2 of improved calcium carbonate, coffee sludge, cork powder, stearic acid, wax, white oil and pigment A first step of mixing for about 15 minutes, a first step of mixing the remaining calcium carbonate 1/2 into a mixer, and a second step of mixing for 5 minutes, and a second step of mixing and extruding the mixed material into an extruder, A third step of extruding the extrudate so as to have a plurality of elastic wings on the outer periphery and having a hole in the elastic wings; A fourth step of cutting the extrudate to a size of 2.5 mm in water; A fifth step of putting the cut rubber chips into a dehydrator and dehydrating them and cooling them at room temperature; The method comprising the steps of: (a) preparing a synthetic rubber composition for artificial grass;
다만, 상기 등록특허는 탄성이 충분하지 않아 마찰력에 의한 부상의 위험이 있다는 문제가 있다.
However, the registered patent has a problem that there is a risk of injury due to frictional force because of insufficient elasticity.
본 발명은 상기한 바와 같은 종래 기술의 문제점을 해결하기 위한 것으로서,본 발명의 목적은 중금속, 다환 방향족 화화물 및 VOC를 함유하지 않으며, 제습력과 가습력이 우수하고 마찰에 의한 정전기 발생이 적고, 항곰팡이 성질 및 물성이 우수한 친환경 인조잔디용 충진재 제조방법을 제공하는 것이다.Disclosure of Invention Technical Problem [8] Accordingly, the present invention has been made keeping in mind the above problems occurring in the prior art, and it is an object of the present invention to provide a polyurethane foam which does not contain heavy metals, polycyclic aromatics and VOCs, has excellent dehumidifying power and humidifying power, , An antifungal property and a physical property.
또한, 본 발명의 목적은 모듈러스 및 인장강도에서 종래 충진재에 비해 우수한 친환경 인조잔디용 충진재 제조방법을 제공하는 것이다.
It is another object of the present invention to provide a method for manufacturing an environmentally friendly artificial turf filler which is superior to conventional fillers in modulus and tensile strength.
상기한 목적을 달성하기 위하여 본 발명에 따른 친환경 인조잔디용 충진재 제조방법은 다공성 구형의 실리카 볼을 마련하는 S1단계와; 나노 금속산화물 3~25중량부와, 유기용매 25~30중량부와, 바인더 10~30중량부를 혼합한 코팅조성물을 마련하는 S2단계와; 상기 S1 단계의 실리카 볼 100중량부를 기준으로 상기 코팅조성물 10~50중량부를 혼합 교반하여 상기 실리카 볼 표면을 금속산화물로 코팅하는 S3단계와; 금속산화물로 표면 코팅된 실리카 볼 5~20중량부와, 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부와, 파라핀 오일 20~25중량부와, 부타디엔 5~15중량부와, 충진 분말 30~40중량부를 혼합한 혼합조성물을 마련하는 S4단계; 상기 혼합조성물을 압출 및 절단하여 칩 형태의 충진재를 제조하는 S5단계;를 포함하는 것을 특징으로 한다.According to an aspect of the present invention, there is provided a method for manufacturing an eco-friendly artificial turf filler material, comprising the steps of: preparing a porous spherical silica ball; 3 to 25 parts by weight of a nano-metal oxide, 25 to 30 parts by weight of an organic solvent, and 10 to 30 parts by weight of a binder; Coating the surface of the silica balls with a metal oxide by mixing and stirring 10 to 50 parts by weight of the coating composition based on 100 parts by weight of the silica balls in the step S1; 5 to 20 parts by weight of a silica ball surface-coated with a metal oxide, 3 to 8 parts by weight of polypropylene, 10 to 13 parts by weight of polyethylene, 20 to 25 parts by weight of paraffin oil, 5 to 15 parts by weight of butadiene, And 30 to 40 parts by weight of a powder; And a step S5 of forming a filling material in the form of a chip by extruding and cutting the mixed composition.
또한, 본 발명에 따른 친환경 인조잔디용 충진재 및 그 제조방법에 있어서, 나노 금속산화물은 적어도 NiO, FeO, Cu2O, TiO2 및 WO3 중에서 적어도 하나가 선택되고, 상기 바인더는 TESPT(bis-(3-triethoxysilpropyl)tetrasulfide)이며, 상기 유기용매는 이염화메탄(dichloromethane)이고, 상기 S3단계는 반응기에 상기 실리카 볼, 상기 나노 금속산화물, 상기 이염화메탄(dichloromethane) 및 상기 TESPT(bis-(3-triethoxysilpropyl)tetrasulfide)를 넣고 1~3시간 동안 교반하여 이루어지는 것을 특징으로 한다.In the filler material for artificial turf grass according to the present invention and the method for manufacturing the same, at least one of NiO, FeO, Cu 2 O, TiO 2 and WO 3 is selected as the nano metal oxide, and the binder is TESPT (bis- (3-triethoxysilylpropyl) tetrasulfide, the organic solvent is dichloromethane, and the step S3 is a step in which the silica balls, the nano-metal oxide, the dichloromethane, and the TESPT 3-triethoxysilpropyl) tetrasulfide) and stirring for 1 to 3 hours.
또한, 본 발명에 따른 친환경 인조잔디용 충진재 및 그 제조방법에 있어서, 충진 분말은 몬모릴로나이트, 일라이트, 게르마늄, 벤토나이트, 클레이(clay) 및 탄산칼슘(CaCO3) 중에서 어느 하나로 이루어지는 것을 특징으로 한다.In the eco-friendly artificial turf filler according to the present invention and the method of manufacturing the same, the fill powder is composed of montmorillonite, ilite, germanium, bentonite, clay and calcium carbonate (CaCO 3 ).
또한, 본 발명에 따른 친환경 인조잔디용 충진재 및 그 제조방법에 있어서, S4단계는 상기 표면 코팅된 실리카 볼 5~20중량부와, 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부와, 파라핀 오일 20~25중량부와, 부타디엔 5~15중량부을 반응기에 넣고 2~5분 동안 1차 교반하는 S4-1단계와, 상기 S4-1단계의 혼합물에 상기 충진 분말을 넣고 2~5분 동안 2차 교반하는 S4-2단계와, 상기 S4-2단계의 혼합물에 첨가제로서 자외선 안정제 1~10중량부와, 산화방지제 0.1~1.5중량부를 넣고 3차 교반하는 S4-3단계와, 상기 S4-3단계의 혼합물에 황 0.1~0.2중량부와, TMTD(Tetramethyl Thiuram Disulfide) 0.1~0.8중량부를 넣고 2~5분 동안 4차 교반하는 S4-4단계를 포함하여 이루어지되, 상기 S4-1단계 내지 S4-4단계에서 상기 반응기의 온도는 55~65℃의 온도로 유지되는 것을 특징으로 한다.
In the step S4, 5 to 20 parts by weight of the surface-coated silica balls, 3 to 8 parts by weight of polypropylene, 10 to 13 parts by weight of polyethylene, 20 to 25 parts by weight of paraffin oil and 5 to 15 parts by weight of butadiene in a reactor and stirring the mixture for 2 to 5 minutes in a primary stage; And 4 to 3 parts by weight of an antioxidant and 0.1 to 1.5 parts by weight of an antioxidant as an additive are added to the mixture of step S4-2 and step S4-3, 0.1 to 0.2 parts by weight of sulfur and 0.1 to 0.8 parts by weight of TMTD (Tetramethyl Thiuram Disulfide) are added to the mixture of step S4-3, and the mixture is stirred for 4 to 4 minutes. The temperature of the reactor is maintained at a temperature of 55 to 65 ° C.
본 발명에서 제안하고 있는 본 발명에 따른 친환경 인조잔디용 충진재 제조방법에 의하면, 본 발명은 상기한 바와 같은 종래 기술의 문제점을 해결하기 위한 것으로서, 중금속, 다환 방향족 화화물 및 VOC를 함유하지 않으며, 제습력과 가습력이 우수하고 마찰에 의한 정전기 발생이 적다. 그리고 항곰팡이 성질 및 물성이 우수한 친환경 인조잔디용 충진재 제조방법을 제공하는 것이다.SUMMARY OF THE INVENTION The present invention has been made in view of the above problems, and it is an object of the present invention to provide a method for manufacturing an environmentally friendly artificial turf filling material according to the present invention, which does not contain heavy metals, polycyclic aromatics and VOCs, It has good dehumidifying power and humidifying power and less static electricity due to friction. And an antifungal property and a physical property, which are excellent in anti-fungal properties and physical properties.
또한, 본 발명은 모듈러스 및 인장강도에서 종래 충진재에 비해 우수하다.
In addition, the present invention is superior to conventional fillers in modulus and tensile strength.
도 1은 본 발명에 따른 친환경 인조잔디용 충진재 제조방법의 각 단계를 도시하는 공정도이다.
도 2는 종래 인조잔디의 구조를 도시하는 도면이다.1 is a process diagram showing each step of a method for manufacturing a filler material for artificial turfgrass according to the present invention.
2 is a view showing the structure of a conventional artificial turf.
이하 본 발명의 바람직한 실시예에 대하여 구체적으로 설명한다.Hereinafter, preferred embodiments of the present invention will be described in detail.
본 발명을 설명함에 있어서, 관련된 공지기능 혹은 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우 그 상세한 설명은 생략한다. 또한, 후술되는 용어들은 본 발명에서의 기능을 고려하여 정의된 용어들로서 이는 사용자, 운용자의 의도 또는 판례 등에 따라 달라질 수 있다. 그러므로 그 정의는 본 명세서 전반에 걸친 내용을 토대로 내려져야 할 것이다.
In the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear. In addition, the terms described below are defined in consideration of the functions of the present invention, and these may vary depending on the intention of the user, the operator, or the precedent. Therefore, the definition should be based on the contents throughout this specification.
도 1은 본 발명에 따른 친환경 인조잔디용 충진재 제조방법의 각 단계를 도시하는 공정도이다.1 is a process diagram showing each step of a method for manufacturing a filler material for artificial turfgrass according to the present invention.
도 1을 참조하면, 본 발명에 따른 친환경 인조잔디용 충진재 제조방법은 다공성 구형의 실리카 볼을 마련하는 S1단계와, 상기 나노 금속산화물 3~25중량부와, 유기용매 25~30중량부와, 바인더 10~30중량부를 혼합한 코팅조성물을 마련하는 S2단계와, 상기 S1 단계의 실리카 볼 100중량부를 기준으로 상기 코팅조성물 10~50중량부를 혼합 교반하여 상기 실리카 볼 표면을 코팅하는 S3단계와, 상기 표면 코팅된 실리카 볼 5~20중량부와, 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부와, 파라핀 오일 20~25중량부와, 부타디엔 5~15중량부와, 충진 분말 30~40중량부를 혼합한 혼합조성물을 마련하는 S4단계, 상기 혼합조성물을 압출 및 절단하여 칩 형태의 충진재를 제조하는 S5단계를 포함할 수 있다.Referring to FIG. 1, the method for preparing a synthetic filler for artificial turf according to the present invention comprises the steps of: (1) providing a porous spherical silica ball; (2) 3 to 25 parts by weight of the nano metal oxide; A step S2 of preparing a coating composition comprising 10 to 30 parts by weight of a binder, and 10 to 50 parts by weight of the coating composition based on 100 parts by weight of the silica ball in the step S1, 5 to 20 parts by weight of the surface-coated silica balls, 3 to 8 parts by weight of polypropylene, 10 to 13 parts by weight of polyethylene, 20 to 25 parts by weight of paraffin oil, 5 to 15 parts by weight of butadiene, To 40 parts by weight of a mixed composition; and a step S5 of producing a filler in the form of a chip by extruding and cutting the mixed composition.
본 발명의 친환경 인조잔디용 충진재 제조방법에 따라 제조된 충진재는 중금속, 다환 방향족 화화물 및 VOC를 함유하지 않으며, 제습력과 가습력이 우수하고 마찰에 의한 정전기 발생이 적다. 그리고 항곰팡이 성질 및 기계적 물성이 우수한 장점이 있다.The filler prepared according to the method for manufacturing an artificial turf filler material of the present invention does not contain heavy metals, polycyclic aromatic compounds and VOCs, has excellent dehumidifying power and humidifying power, and generates less static electricity due to friction. And excellent antifungal properties and mechanical properties.
상기 S1단계에서 SCMS(solid core-mesoporous shell)구조의 실리카 볼은 스퇴버법 (Stober-Bohn-Fink)을 통해 제조되는 것을 예시할 수 있는데, 실리카 전구체인 테트라에틸 오르쏘실리케이트(tetraethyl orthosilicate, TEOS)가 알카리성 촉매를 첨가한 수성-알카리성 용매에서 가수분해되면서 실리카 볼이 형성되며, 촉매로서 암모니아수(NH3), 수산화나트륨(NaOH) 등이 사용되는 것을 예시할 수 있으며, 그 입경은 50 nm ~ 10㎛ 인 것을 예시할 수 있으나, 50~1,000nm인 것이 바람직하다.The silica balls having a solid core-mesoporous shell (SCMS) structure may be prepared by a Stober-Bohn-Fink method. The silica precursor, tetraethyl orthosilicate (TEOS) (NH 3), sodium hydroxide (NaOH) or the like is used as the catalyst, and the particle diameter is 50 nm to 10 탆 , But it is preferably 50 to 1,000 nm.
상기 S2단계의 상기 나노 금속산화물은 NiO, FeO, Cu2O, TiO2 및 WO3 중에서 적어도 하나가 선택될 수 있다.At least one of NiO, FeO, Cu 2 O, TiO 2 and WO 3 may be selected as the nano metal oxide in the step S 2 .
그리고 상기 바인더는 TESPT(bis-(3-triethoxysilpropyl)tetrasulfide)이며, 상기 유기용매는 이염화메탄(dichloromethane)인 것을 예시할 수 있다.The binder may be TESPT (bis- (3-triethoxysilpropyl) tetrasulfide), and the organic solvent may be dichloromethane.
상기 S2단계의 코팅조성물은 차열 기능과 자성 기능을 갖게 되며, 나노 금속산화물의 분산을 위해 분산제를 소량 첨가할 수 있다.The coating composition of step S2 has a heat shielding function and a magnetic function, and a small amount of a dispersing agent may be added to disperse the nano-metal oxide.
상기 S3단계에서는 상기 실리카 볼 표면의 수산화기와 상기 코팅조성물의 TESPT의 에톡시기가 반응하게 되는데, 보다 구체적으로 반응기에 상기 실리카 볼, 상기 나노 금속산화물, 상기 이염화메탄(dichloromethane) 및 상기 TESPT(bis-(3-triethoxysilpropyl)tetrasulfide)를 넣고 1~3시간 동안 저속으로 교반하여 실리카 볼 표면의 코팅이 이루어진다.In step S3, the hydroxyl group of the silica ball surface reacts with the ethoxy group of TESPT of the coating composition. More specifically, the silica balls, the nano metal oxide, the dichloromethane, and the bis (bis - (3-triethoxysilpropyl) tetrasulfide) and stirred at low speed for 1 to 3 hours to coat the surface of the silica balls.
상기 S4단계는 상기 표면 코팅된 실리카 볼과 고분자 합성 원료를 혼합하여 혼합조성물을 마련하는 것으로서, 상기 고분자 합성 원료는 폴리올레핀, 오일, 부타디엔, 충진 분말, 첨가제, 황, 촉진제인 것을 예시할 수 있다.The step S4 is a step of preparing a mixed composition by mixing the surface-coated silica balls with a polymer synthesis starting material. The polymer synthesis starting material may be a polyolefin, an oil, a butadiene, a filler powder, an additive, a sulfur or an accelerator.
상기 표면 코팅된 실리카 볼은 기존의 카본 블랙과는 달리, 고분자와 함께 3차원 사슬구조를 형성함으로써 탄성 구조 및 내충격성을 보다 향상시키는 장점이 있다.Unlike conventional carbon black, the surface-coated silica balls have the advantage of improving the elastic structure and impact resistance by forming a three-dimensional chain structure together with the polymer.
상기 폴리올레핀은 폴리프로필렌과, 폴리에틸렌을 혼합하는 것이 바람직한데, 폴리프로필렌은 경질성(hard segment)을 제공하고 상기 폴리에틸렌은 연질성(soft segment)를 제공하는 것으로서, 각각 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부인 것을 예시할 수 있다. 보다 바람직하게는 폴리프로필렌과, 폴리에틸렌이 1 : 1.5 ~ 3 중량비인 것이 바람직하고, 상기 폴리프로필렌이 폴리에틸렌보다 3배를 초과하는 경우에는 탄성이 줄고 인체와 접촉시 마찰로 인해 부상 위험이 커지고, 1.5배 미만인 경우에는 내구성이 약해지기 때문이다. 또한, 열가소성의 폴리올레핀을 사용함으로써 재활용이 가능한 장점이 있다.Preferably, the polyolefin is a blend of polypropylene and polyethylene, wherein the polypropylene provides a hard segment and the polyethylene provides a soft segment, wherein each polypropylene comprises 3 to 8 parts by weight of polypropylene, , And 10 to 13 parts by weight of polyethylene. More preferably, the polypropylene and polyethylene are in a ratio of 1: 1.5 to 3 by weight, and when the polypropylene is more than 3 times the polyethylene, the elasticity is reduced and the risk of injury is increased due to friction when contacted with a human body. If it is less than twice, the durability becomes weak. Further, the use of a thermoplastic polyolefin has the advantage of being recyclable.
상기 오일은 연화제로서 작용하는 것으로서, 갈라짐을 방지하고 가공성을 향상시키는 역할을 하는 것으로서, 파라핀 오일인 것을 예시할 수 있다. 상기 오일이 20중량부 미만인 경우에는 상기 갈라짐 및 가공성 향상의 효과를 기대하기 어렵고, 25중량부를 초과하는 경우에는 오히려 물성 저하의 원인이 되므로 20~25중량부로 제한하는 것이 바람직하다.The oil serves as a softening agent and serves to prevent cracking and improve workability, and examples thereof include paraffin oil. When the amount of the oil is less than 20 parts by weight, the effect of improving the cracking and workability is not expected. When the amount of the oil is more than 25 parts by weight, it is preferable to restrict the amount of the oil to 20 to 25 parts by weight.
상기 첨가제는 자외선 안정제와, 산화방지제인 것을 예시할 수 있다.Examples of the additive include an ultraviolet stabilizer and an antioxidant.
상기 자외선 안정제는 자외선에 의한 폴리올레핀의 분해를 방지하기 위한 것으로서, 벤조트리아졸(benzotriazoles), 벤조페논(benzophenone) 등을 예시할 수 있다.The ultraviolet stabilizer is for preventing decomposition of polyolefin by ultraviolet rays, and examples thereof include benzotriazoles, benzophenone, and the like.
상기 산화방지제는 공기 중 산소에 의해 산화열화를 받는 것을 방지하기 위한 것으로서, BHT(2.6-di-t-Butyl-4-methylphenol)인 것을 예시할 수 있다.The antioxidant may be BHT (2.6-di-t-butyl-4-methylphenol) to prevent oxidative degradation by oxygen in the air.
상기 충진 분말은 몬모릴로나이트, 일라이트, 게르마늄, 벤토나이트, 클레이(clay) 및 탄산칼슘(CaCO3) 중에서 어느 하나로 이루어지는 것을 예시할 수 있다. 이들 분말은 단순한 충진재 역할 뿐만 아니라, 가열시 다량의 원적외선을 방사한다.The filler powder may be composed of any one of montmorillonite, ilite, germanium, bentonite, clay and calcium carbonate (CaCO 3 ). These powders not only serve as fillers but also emit a large amount of far infrared rays upon heating.
그리고 상기 충진 분말에는 상기 코팅조성물에 함유된 나노 금속산화물과는 별개로 TiO2와 WO3와 같은 광촉매를 더 포함하는 것이 바람직한데, 이때 실내 운동장과 같은 환경에서는 TiO2와 WO3가 광촉매 작용을 하기 힘들기 때문에 TiO2와 WO3와 1 : 0.2 ~ 0.3 중량비로 혼합하여 가시광에서도 광촉매 작용을 할 수 있도록 구성하는 것이 바람직하다.It is preferable that the filled powder further contains a photocatalyst such as TiO 2 and WO 3 separately from the nano-metal oxide contained in the coating composition. In an environment such as an indoor playground, TiO 2 and WO 3 may act as a photocatalyst It is preferable to mix TiO 2 and WO 3 at a weight ratio of 1: 0.2-0.3 so that the photocatalytic action can be performed even in visible light.
상기 촉진재는 가류 속도와 가교 밀도를 향상시키는 역할을 하는 것으로서, TMTD(Tetramethyl-Thiuram-Disulfide), MBTS (2,2-dithiobis(benzo-thiazole)), CBS(n-cyclohexyl benzothiazyl-2-sulfenamide) 등을 예시할 수 있으나, 이 중에서 TMTD를 사용하는 것이 탄성 및 인장 성능이 가장 향상시킬 수 있다.The accelerator has the function of improving the vulcanization rate and the cross-linking density, and it is preferable that the promoting material is selected from the group consisting of TMTD (Tetramethyl-Thiuram-Disulfide), MBTS (2,2-dithiobis (benzo-thiazole)), CBS (n-cyclohexyl benzothiazyl- , Etc. Among them, the use of TMTD can maximally improve the elasticity and tensile performance.
구체적으로, 상기 S4단계는 상기 표면 코팅된 실리카 볼 5~20중량부와, 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부와, 파라핀 오일 20~25중량부와, 부타디엔 5~15중량부을 반응기에 넣고 2~5분 동안 1차 교반하는 S4-1단계와, 상기 S4-1단계의 혼합물에 상기 충진 분말을 넣고 2~5분 동안 2차 교반하는 S4-2단계와, 상기 S4-2단계의 혼합물에 첨가제로서 자외선 안정제 1~10중량부와, 산화방지제 0.1~1.5중량부를 넣고 3차 교반하는 S4-3단계와, 상기 S4-3단계의 혼합물에 황 0.1~0.2중량부와, TMTD(Tetramethyl Thiuram Disulfide) 0.1~0.8중량부를 넣고 2~5분 동안 4차 교반하는 S4-4단계를 포함하여 이루어지는 것을 예시할 수 있다.Specifically, in step S4, 5 to 20 parts by weight of the surface-coated silica balls, 3 to 8 parts by weight of polypropylene, 10 to 13 parts by weight of polyethylene, 20 to 25 parts by weight of paraffin oil, A step S4-1 of adding a part by weight of the powder to the reactor in the step S4-1 and a step S4-2 of stirring the mixture for 2 to 5 minutes, 1 to 10 parts by weight of an ultraviolet stabilizer as an additive and 0.1 to 1.5 parts by weight of an antioxidant are added to the mixture of Step 2 and Step S3-3, and 0.1 to 0.2 parts by weight of sulfur is added to the mixture of Step S4-3 And 0.1 to 0.8 parts by weight of TMTD (Tetramethyl Thiuram Disulfide), and stirring the mixture for 4 to 5 minutes.
상기 S4단계를 통해 고분자 중합이 이루어지면서 SCMS-실란-고분자의 3차원 사슬 구조를 형성하여 가교 밀도가 증가하여 물성 향상을 기대할 수 있다.
As a result of polymeric polymerization through step S4, a three-dimensional chain structure of the SCMS-silane-polymer is formed, and the crosslinking density is increased to improve the physical properties.
상기 S5단계는 상기 복합체를 압출 및 절단하여 입도가 1~5mm인 칩 형태의 충진재를 제조하게 된다.
In step S5, the composite is extruded and cut to produce a filler having a chip size of 1 to 5 mm in particle size.
이하에서는 본 발명에 따른 친환경 인조잔디용 충진재 제조방법의 바람직한 실시예를 상세히 설명한다.Hereinafter, a preferred embodiment of a method of manufacturing a filler material for artificial turfgrass according to the present invention will be described in detail.
1) SCMS(Solid core/mesoporous shell)구조이고 평균 입도가 100nm인 실리카 볼을 마련한다.1) A silica ball having a solid core / mesoporous shell (SCMS) structure and an average particle size of 100 nm is prepared.
구체적으로 실리카 볼은 반응조를 30℃로 유지하고 에틸알콜 25 mole%와, tetraethyl orthosilicate(TEOS) 6 mole%를 넣으면서 교반한 다음, 증류수 65 mole%를 천천히 dropping 한 다음, HCl 0.2 mole%를 dropping 한 후 50℃로 승온하고, 5시간 동안 교반하여 다공성 구형 실리카 볼을 얻게 된다.Specifically, the silica balls were stirred while adding 25 mole% of ethyl alcohol and 6 mole% of tetraethyl orthosilicate (TEOS) while maintaining the reaction temperature at 30 ° C., slowly dropping 65 mole% of distilled water, dropping 0.2 mole% of HCl Thereafter, the temperature was raised to 50 ° C, and the mixture was stirred for 5 hours to obtain porous spherical silica balls.
2) 제1반응기에 TiO2 및 WO3를 1 : 0.2의 중량비로 이루어진 나노 금속산화물 15중량부와, 이염화메탄(dichloromethane) 25중량부를 넣고 70℃에서 3시간 동안 교반하여 겔 형태의 나노 금속산화물을 만들고, 분산제 1.5중량부와, TESPT(bis-(3-triethoxysilpropyl)tetrasulfide)를 25중량부를 넣고 상온에서 혼합하여 코팅조성물을 마련한다.2) In a first reactor, 15 parts by weight of a nano-metal oxide consisting of TiO 2 and WO 3 in a weight ratio of 1: 0.2 and 25 parts by weight of dichloromethane were mixed and stirred at 70 ° C for 3 hours to prepare a gel- Oxide, 1.5 parts by weight of a dispersant and 25 parts by weight of bis- (3-triethoxysilpropyl) tetrasulfide (TESPT) were mixed and mixed at room temperature to prepare a coating composition.
3) 제1반응기를 70℃로 승온한 다음, 실리카 볼 100중량부를 넣고 2시간 동안 교반하여 실리카 볼 표면을 코팅한다.3) After raising the temperature of the first reactor to 70 ° C, 100 parts by weight of silica balls are added and stirred for 2 hours to coat the surface of the silica balls.
4) 제2반응기 내 온도를 60℃로 유지한 상태에서 상기 표면 코팅된 실리카 볼 15중량부와, 폴리프로필렌 5중량부와, 폴리에틸렌 110량부와, 파라핀 오일 20중량부와, 부타디엔 5중량부를 넣고 5분 동안 1차 교반한다.4) While keeping the temperature in the second reactor at 60 占 폚, 15 parts by weight of the surface-coated silica balls, 5 parts by weight of polypropylene, 110 parts by weight of polyethylene, 20 parts by weight of paraffin oil and 5 parts by weight of butadiene Stir for 5 minutes.
그리고 반응기에 충진 분말로서 일라이트 25중량부와 몬모릴로나이트 10중량부를 넣고, 5분 동안 2차 교반한다.Then, 25 parts by weight of i-lamp and 10 parts by weight of montmorillonite were added as a powder to be charged in the reactor, and the mixture was stirred for 5 minutes.
그리고 반응기에 벤조트리아졸(benzotriazoles) 2중량부와, BHT(2.6-di-t-Butyl-4-methylphenol) 0.5중량부를 넣고, 1분 동안 3차 교반한다.Then, 2 parts by weight of benzotriazoles and 0.5 part by weight of BHT (2.6-di-t-butyl-4-methylphenol) were added to the reactor and stirred for one minute.
그리고 황 0.1중량부와, TMTD(Tetramethyl Thiuram Disulfide) 0.5중량부를 넣고 2분 동안 4차 교반하여 혼합조성물을 마련한다.0.1 part by weight of sulfur and 0.5 part by weight of TMTD (Tetramethyl Thiuram Disulfide) were added and stirred for 4 minutes to prepare a mixed composition.
5) 상기 혼합조성물을 압출 및 절단하여 입도가 5mm인 충진재를 제조한다.
5) The mixed composition is extruded and cut to prepare a filler having a particle size of 5 mm.
[비교예 1][Comparative Example 1]
상기 실시예 1에서 표면 코팅된 실리카 대신 카본 블랙을 사용한 것을 제외하고, 실시예 1과 동일하게 충진재를 제조하였다.
A filler was prepared in the same manner as in Example 1 except that carbon black was used in place of the surface-coated silica in Example 1.
[비교예 2][Comparative Example 2]
상기 실시예 1에서 표면 코팅되지 않은 실리카 볼을 사용한 것을 제외하고, 실시예 1과 동일하게 충진재를 제조하였다.
A filler was prepared in the same manner as in Example 1, except that the silica balls not coated with the surface were used in Example 1 above.
이하에서는 실시예 1에서 제조된 충진재의 물성을 측정하였다.Hereinafter, physical properties of the filler prepared in Example 1 were measured.
[실험예 1][Experimental Example 1]
제조된 충진재를 만능인장기(universal testing machine, Instron 3365)를 이용하여 100, 300% 모듈러스, 인장강도, 신장율을 측정하였고, 그 결과는 아래 표 1에 정리하였다.
The prepared fillers were measured for 100, 300% modulus, tensile strength and elongation using a universal testing machine (Instron 3365). The results are summarized in Table 1 below.
(MPa)100% Modulus
(MPa)
(MPa)300% Modulus
(MPa)
(MPa)Tensile strength
(MPa)
(%)Elongation
(%)
위 표 1에서 확인할 수 있듯이 본 발명의 실시예 1의 충진재가 모듈러스 및 인장강도에서 비교예 1, 2에 비해 현저한 특성을 가진다는 것을 알 수 있다.
As can be seen from the above Table 1, it can be seen that the filler of Example 1 of the present invention has remarkable characteristics at the modulus and tensile strength as compared with Comparative Examples 1 and 2.
이상에서 설명된 본 발명은 예시적인 것에 불과하며, 본 발명이 속한 기술분야의 통상의 지식을 가진 자라면 이로부터 다양한 변형 및 균등한 타 실시예가 가능하다는 점을 잘 알 수 있을 것이다. 그러므로 본 발명은 상기의 상세한 설명에서 언급되는 형태로만 한정되는 것은 아님을 잘 이해할 수 있을 것이다. 따라서 본 발명의 진정한 기술적 보호 범위는 첨부된 특허청구범위의 기술적 사상에 의해 정해져야 할 것이다. 또한, 본 발명은 첨부된 청구범위에 의해 정의되는 본 발명의 정신과 그 범위 내에 있는 모든 변형물과 균등물 및 대체물을 포함하는 것으로 이해되어야 한다.
While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed exemplary embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the invention. Therefore, it is to be understood that the present invention is not limited to the above-described embodiments. Accordingly, the true scope of the present invention should be determined by the technical idea of the appended claims. It is also to be understood that the invention includes all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Claims (5)
나노 금속산화물 15중량부와, 유기용매 25중량부와, 바인더 25중량부를 혼합한 코팅조성물을 마련하는 S2단계와;
상기 S1 단계의 실리카 볼 100중량부를 기준으로 상기 코팅조성물 10~50중량부를 혼합 교반하여 상기 실리카 볼 표면을 금속산화물로 코팅하는 S3단계와;
상기 표면 코팅된 실리카 볼 5~20중량부와, 폴리프로필렌 3~8중량부와, 폴리에틸렌 10~13중량부와, 파라핀 오일 20~25중량부와, 부타디엔 5~15중량부을 반응기에 넣고 2~5분 동안 1차 교반하는 S4-1단계와, 상기 S4-1단계의 혼합물에 상기 충진 분말을 넣고 2~5분 동안 2차 교반하는 S4-2단계와, 상기 S4-2단계의 혼합물에 첨가제로서 자외선 안정제 1~10중량부와, 산화방지제 0.1~1.5중량부를 넣고 3차 교반하는 S4-3단계와, 상기 S4-3단계의 혼합물에 황 0.1~0.2중량부와, 테트라메틸티우람디설파이드(Tetramethyl Thiuram Disulfide) 0.1~0.8중량부를 넣고 2~5분 동안 4차 교반하는 S4-4단계를 수행하여 혼합조성물을 마련하되, 상기 S4-1단계 내지 S4-4단계에서 상기 반응기의 온도는 55~65℃의 온도로 유지되는 S4단계; 및
상기 혼합조성물을 압출 및 절단하여 칩 형태의 충진재를 제조하는 S5단계;를 포함하는 것을 특징으로 하는 친환경 인조잔디용 충진재 제조방법.
Providing a porous spherical silica ball;
15 parts by weight of a nano-metal oxide, 25 parts by weight of an organic solvent, and 25 parts by weight of a binder;
Coating the surface of the silica balls with a metal oxide by mixing and stirring 10 to 50 parts by weight of the coating composition based on 100 parts by weight of the silica balls in the step S1;
5 to 20 parts by weight of the surface-coated silica balls, 3 to 8 parts by weight of polypropylene, 10 to 13 parts by weight of polyethylene, 20 to 25 parts by weight of paraffin oil and 5 to 15 parts by weight of butadiene, A step S4-2 of first stirring the mixture for 5 minutes, a step S4-2 of adding the filled powder to the mixture of the step S4-1 and the second stirring for 2 to 5 minutes, 1 to 10 parts by weight of an ultraviolet stabilizer and 0.1 to 1.5 parts by weight of an antioxidant are added to the mixture of step S4-3 and step S3-3, and 0.1 to 0.2 parts by weight of sulfur are mixed with tetramethylthiuram disulfide The temperature of the reactor in steps S4-1 to S4-4 is in the range of 55 to 100 ° C., Maintaining the temperature at 65 [deg.] C; And
And a step S5 of forming a filling material in the form of a chip by extruding and cutting the mixed composition.
상기 충진 분말은 몬모릴로나이트, 일라이트, 게르마늄, 벤토나이트, 클레이(clay) 및 탄산칼슘(CaCO3) 중에서 어느 하나로 이루어지는 것을 특징으로 하는 친환경 인조잔디용 충진재 제조방법.
The method according to claim 1,
Wherein the filling powder is composed of any one of montmorillonite, ilite, germanium, bentonite, clay and calcium carbonate (CaCO 3 ).
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