KR102128520B1 - Non-combustible spray coating material and manufacturing method of the same - Google Patents

Non-combustible spray coating material and manufacturing method of the same Download PDF

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KR102128520B1
KR102128520B1 KR1020180103173A KR20180103173A KR102128520B1 KR 102128520 B1 KR102128520 B1 KR 102128520B1 KR 1020180103173 A KR1020180103173 A KR 1020180103173A KR 20180103173 A KR20180103173 A KR 20180103173A KR 102128520 B1 KR102128520 B1 KR 102128520B1
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mixture
macsumsuk
powder
granules
extract
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KR20200026392A (en
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이명희
이승훈
장혜영
최승희
박정주
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    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
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    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
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Abstract

본 발명은 펄라이트, 버미큘라이트, 세피올라이트의 혼합으로 이루어진 팽창성 광물을 분쇄하여 팽창시킨 광물 미분말, 불연성 혼합물, 불연성 수지 및 천연결합재의 혼합으로 조성되는 불연성 뿜칠재와,
펄라이트, 버미큘라이트, 세피올라이트를 이용하여 광물 미분말을 제조하고; 다공질의 맥섬석 과립을 제조하고; 상기 다공질의 맥섬석 과립을 이용하여 불연성 혼합물을 제조하고; LDPE/EVA 수지, 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 혼합하여 불연성 수지를 제조하고; 송진, 아교 및 어교의 혼합물, 항균추출물을 혼합하여 천연결합재를 제조하고; 상기 미분말 팽창성광물 혼합물, 불연성 혼합물, 불연성 수지, 천연결합재를 혼합하여 불연성 뿜칠재를 제조함으로써 이루어지는 불연성 뿜칠재 제조방법에 관한 것이다.
The present invention is a non-combustible spray coating material composed of a mixture of a fine mineral powder, a non-combustible mixture, a non-combustible resin, and a natural binder obtained by crushing and expanding an expandable mineral composed of a mixture of pearlite, vermiculite, and sepiolite,
To prepare a fine mineral powder using pearlite, vermiculite, and sepiolite; To prepare porous Macsumsuk granules; Preparing a non-flammable mixture using the porous macsumsuk granules; LDPE/EVA resin, magnesium hydroxide, dispersant, fumed silica of a flame retardant aid, and an antioxidant are mixed to prepare a non-flammable resin; To prepare a natural binder by mixing a mixture of rosin, glue and fish, and an antibacterial extract; The present invention relates to a method for producing a non-flammable spray coating material by mixing the fine powder intumescent mineral mixture, a non-combustible mixture, a non-combustible resin, and a natural binder to prepare a non-flammable spray coating material.

Description

불연성 뿜칠재 및 이의 제조방법{NON-COMBUSTIBLE SPRAY COATING MATERIAL AND MANUFACTURING METHOD OF THE SAME}Non-combustible spray coating material and its manufacturing method {NON-COMBUSTIBLE SPRAY COATING MATERIAL AND MANUFACTURING METHOD OF THE SAME}

본 발명은 펄라이트, 버미큘라이트, 세피올라이트의 혼합으로 이루어진 팽창성 광물을 분쇄하여 팽창시킨 광물 미분말, 불연성 혼합물, 불연성 수지 및 천연결합재의 혼합으로 조성되는 불연성 뿜칠재와,The present invention is a non-combustible spray coating material composed of a mixture of a fine mineral powder, a non-combustible mixture, a non-combustible resin, and a natural binder obtained by crushing and expanding an expandable mineral composed of a mixture of pearlite, vermiculite, and sepiolite,

펄라이트, 버미큘라이트, 세피올라이트를 이용하여 광물 미분말을 제조하고; 다공질의 맥섬석 과립을 제조하고; 상기 다공질의 맥섬석 과립을 이용하여 불연성 혼합물을 제조하고; LDPE/EVA 수지, 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 혼합하여 불연성 수지를 제조하고; 송진, 아교 및 어교의 혼합물, 항균추출물을 혼합하여 천연결합재를 제조하고; 상기 미분말 팽창성광물 혼합물, 불연성 혼합물, 불연성 수지, 천연결합재를 혼합하여 불연성 뿜칠재를 제조함으로써 이루어지는 불연성 뿜칠재 제조방법에 관한 것이다.To prepare a fine mineral powder using pearlite, vermiculite, and sepiolite; To prepare porous Macsumsuk granules; Preparing a non-flammable mixture using the porous macsumsuk granules; LDPE/EVA resin, magnesium hydroxide, dispersant, fumed silica of a flame retardant aid, and an antioxidant are mixed to prepare a non-flammable resin; To prepare a natural binder by mixing a mixture of rosin, glue and fish, and an antibacterial extract; The present invention relates to a method for producing a non-flammable spray coating material by mixing the fine powder intumescent mineral mixture, a non-combustible mixture, a non-combustible resin, and a natural binder to prepare a non-flammable spray coating material.

뿜칠 공법(Sprayed, Shotcrete)은 굳지 않은 페이스트, 모르타르 및 콘크리트를 거푸집을 이용하지 않고 압축공기를 이용하여 시공면에 세밀하고 균일하게 뿜어 붙이는 공법을 말한다.Sprayed, Shotcrete refers to a method in which paste, mortar, and concrete that are not solidified are sprayed on the construction surface in detail and uniformly using compressed air without using a formwork.

건식 공법은 시멘트와 기건 상태의 골재를 잘 혼합(건식혼합)한 후 급결제를 가하여 분사장치에 공급하고 이것을 압축공기로 호스를 통해 압축하여 노즐에서 분사하는 공법이다. 이때 배합수는 노즐 내에서 골재와 혼합되어 시공면에 고속으로 뿜어 붙게된다.In the dry method, cement and air-dried aggregate are well mixed (dry mixed), and then a quick setting agent is added to the injection device, which is compressed through a hose with compressed air and sprayed from the nozzle. At this time, the mixed water is mixed with the aggregate in the nozzle and sprayed onto the construction surface at high speed.

습식 공법은 공기 압송식 및 Screw pump 압송식 공법으로 대별되는 것으로서, 물을 첨가하여 모든 재료를 잘 혼합한 후 분사장치에 공급하고 노즐에서 공기를 더 가하여 분사속도를 증가시켜 뿜어 붙인다. 특히 공기 압송식 습식 공법은 Wet-mixed 덩어리 또는 콘크리트를 압축공기로 압송하여 노즐부에서 급결제를 가하여 뿜어 붙이는 방식으로 습식 Chamber형과 Screw 형 등이 있다.The wet method is roughly classified into the air pressure feed method and the screw pump pressure feed method. After adding water to mix all the materials well, supply it to the spraying device, and add air from the nozzle to increase the spraying speed. Particularly, the air-pressure type wet method is a method in which wet-mixed lumps or concrete are compressed with compressed air, and a quick setting agent is applied from the nozzle and sprayed. There are a wet chamber type and a screw type.

본 발명과 관련하여, 대한민국 등록특허 10-1686447(등록일자 2015.12.08) '불연성 스프레이 몰탈 보온 충전재, 이를 이용한 불연성 보드 및 샌드위치 패널'; 대한민국 등록특허 10-1766316(등록일자 2017.08.02) '가연성 유기 발포 단열재에 부착성이 우수한 불연성 뿜칠 모르타르 및 그의 제조 방법'; 대한민국 등록특허 10-1876205(등록일자 2018.07.03) '솔잎분말이 함유된 불연성 스프레이 몰탈 보온재, 이를 이용한 건축용 보드 및 샌드위치 패널';에 대한 기술이 개시된 바 있다.In connection with the present invention, Republic of Korea Patent Registration 10-1686447 (registration date 2015.12.08)'Non-combustible spray mortar insulating filler, non-combustible board and sandwich panel using the same'; Republic of Korea Patent Registration 10-1766316 (registration date 2017.08.02)'Non-combustible sprayable mortar with excellent adhesion to combustible organic foam insulation and its manufacturing method'; Republic of Korea Patent Registration 10-1876205 (registration date 2018.07.03)'Non-combustible spray mortar insulation material containing pine needle powder, construction boards and sandwich panels using the same' has been disclosed.

대한민국 등록특허 10-1686447(등록일자 2015.12.08)Korean Patent Registration 10-1686447 (Registration date 2015.12.08) 대한민국 등록특허 10-1766316(등록일자 2017.08.02)Republic of Korea Patent Registration 10-1766316 (Registration date 2017.08.02) 대한민국 등록특허 10-1876205(등록일자 2018.07.03)Korean Patent Registration 10-1876205 (Registration Date 2018.07.03)

본 발명은 펄라이트, 버미큘라이트, 세피올라이트의 혼합으로 이루어진 팽창성 광물을 분쇄하여 팽창시킨 광물 미분말, 불연성 혼합물, 불연성 수지 및 천연결합재의 혼합으로 조성함으로써 불연성이 우수하고 뿜칠시공성이 뛰어나며, 항균 특성 및 천연물질 사용에 따른 사용안전성이 뛰어난 불연성 뿜칠재를 제공하고, 이의 제조방법을 제공하고자 하는 것을 발명의 목적으로 한다.The present invention is composed of a mixture of fine mineral powder, non-combustible mixture, non-combustible resin and natural binder by pulverizing and expanding an expandable mineral composed of a mixture of perlite, vermiculite, and sepiolite. It is an object of the invention to provide a non-flammable spray coating material having excellent safety in use according to the use of a material, and to provide a method for manufacturing the same.

상기 목적을 달성하기 위하여,To achieve the above object,

본 발명은 펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%를 혼합하여 100.0 wt%로 조성된 평균입도 200 ~ 1000 mesh의 미분말 혼합물을 800 ℃ ~ 1,200 ℃로 가열하여 팽창시킨 광물 미분말(A) 25.0 ~ 50.0 wt%;The present invention is a mixture of 1.0 to 50.0 wt% of pearlite, 1.0 to 50.0 wt% of vermiculite, and 1.0 to 50.0 wt% of sepiolite to prepare a fine powder mixture having an average particle size of 200 to 1000 mesh at 100.0 wt% at 800 ℃ to 1,200 25.0 ~ 50.0 wt% of the fine mineral powder (A) expanded by heating at °C;

정제수 10.0 ~ 50.0 wt%와, 수산화마그네슘 10.0 ~ 30.0 wt%와, 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 혼합물(B) 40.0 ~ 70.0 wt%;10.0 to 50.0 wt% of purified water, 10.0 to 30.0 wt% of magnesium hydroxide, 10.0 to 30.0 wt% of porous macsumsuk granules, 10.0 to 30.0 wt% of sodium silicate, and 10.0 to 30.0 wt% of urea resin are mixed to form 100.0 wt% Non-combustible mixture (B) 40.0 to 70.0 wt%;

LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 수지(C) 2.0 ~ 5.0 wt%;LDPE/EVA resin 50.0 ~ 70.0 wt%, magnesium hydroxide 25.0 ~ 45.0 wt%, dispersant 0.01 ~ 2.0 wt%, flame retardant fumed silica 0.01 ~ 2.0 wt%, antioxidant 0.01 ~ 2.0 2.0 to 5.0 wt% of a non-combustible resin (C) composed of 100.0 wt% by mixing wt%;

송진(d1) 30.0 ~ 68.0 wt%와, Rosin (d1) 30.0 ~ 68.0 wt% and,

아교와 어교를 1:1 중량비로 혼합한 혼합물(d2) 30.0 ~ 68.0 wt%와, A mixture (d2) 30.0 ~ 68.0 wt% of a mixture of glue and fish glue in a 1:1 weight ratio,

건조시켜 세절한 편백나무 잎을 아세톤에 침적시키되, 편백나무 잎과 70 % 아세톤을 1: 10 ~ 30배의 중량비로 혼합 조성하여 상온에서 4 ~ 6일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 편백나무 추출물과,The dried and shredded cypress leaves are immersed in acetone, but the cypress leaves and 70% acetone are mixed in a weight ratio of 1: 10 to 30 times, and extracted twice at room temperature for 4 to 6 days, and the extract is used with filter paper. Cypress tree extract prepared as a powder by filtering with (filter paper) and drying under reduced pressure,

건조시켜 세절한 약쑥을 에탄올에 침적시키되, 약쑥과 95 % 에탄올을 1 : 8 ~ 12의 중량비로 하여 상온에서 1 ~ 3일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 약쑥 추출물과,Dried fine mugwort was immersed in ethanol, but extracted twice for 1 to 3 days at room temperature with a weight ratio of 1: 8 to 12 of wormwood and 95% ethanol, and the extract was filtered with filter paper. , Wormwood extract prepared as a powder by drying under reduced pressure,

박하와 80 % 에탄올을 1 : 15 ~ 30 중량비로 혼합 조성하여 2 ~ 5 시간 동안 환류추출하고, 추출액을 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 박하추출물을 3:5:2 중량비율로 혼합하여 조성한 항균추출물(d3) 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반 혼합(d1+d2+d3)하여 100.0 wt%로 조성된 천연결합재(D) 2.0 ~ 5.0 wt%;의 혼합(A+B+C+D)으로 조성되는 불연성 뿜칠재를 제공한다.Mint and 80% ethanol were mixed in a ratio of 1: 15 to 30 and extracted under reflux for 2 to 5 hours, and the extract was filtered with filter paper and dried under reduced pressure to prepare a powdered peppermint extract. A natural binder composed of 100.0 wt% by stirring and mixing (d1+d2+d3) 0.1 to 2.0 wt% of the antibacterial extract (d3) prepared by mixing at a weight ratio of 5:2 for 20 to 50 minutes at 2,000 to 3,000 rpm ( D) 2.0 ~ 5.0 wt%; It provides a non-flammable spray paint composition composed of a mixture (A + B + C + D).

또한 상기 불연성 뿜칠재의 제조방법으로서,In addition, as a manufacturing method of the non-flammable spray coating,

펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%의 혼합으로 조성된 팽창성 광물을 200 ~ 1000 mesh로 분쇄한 후 800 ℃ ~ 1,200 ℃로 가열, 팽창시켜 광물 미분말을 제조하는 단계(S10)와,An expandable mineral formed by mixing 1.0 to 50.0 wt% of perlite, 1.0 to 50.0 wt% of vermiculite, and 1.0 to 50.0 wt% of sepiolite was pulverized into 200 to 1000 mesh, and then heated and expanded at 800 to 1,200°C. The step of preparing a fine mineral powder (S10),

맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 혼합물을 조성하고, 상기 혼합물을 과립기를 이용하여 80 ~ 120 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 다공질의 맥섬석 과립을 제조하는 단계(S20)와,The raw Macsumsuk stone is pulverized to have an average particle diameter of 30 to 40 µm, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate (CaCO 3 ) or sodium carbonate in the slurry of Macsumsuk powder (Na 2 CO 3 ) or a blowing agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the macsumsuk powder to form a mixture, and the mixture is used in a granulator. After forming the Macsumsuk granules by molding into granules having an average particle diameter of 80 to 120 μm, the Macsumsuk granules are calcined at a temperature range of 1,000 to 1,200° C. to prepare porous Macsumsuk granules (S20),

상기 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 정제수 10.0 ~ 50.0 wt%, 수산화마그네슘 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 불연성 혼합물을 제조하는 단계(S30)와,A step of mixing the porous macsumsuk granules 10.0 to 30.0 wt%, purified water 10.0 to 50.0 wt%, magnesium hydroxide 10.0 to 30.0 wt%, sodium silicate 10.0 to 30.0 wt%, and urea resin 10.0 to 30.0 wt% to prepare a non-combustible mixture (S30) Wow,

LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 융용기에 투입한 후 120 ~ 180 에서 3 ~ 7 분 동안 용융혼합하여 LDPE/EVA 수지를 조성하고, LDPE (low density polyethylene) 40.0 ~ 60.0 wt% and EVA (polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt% were added to the melting machine, and then melt-mixed at 120 ~ 180 for 3 ~ 7 minutes to form LDPE/EVA resin,

상기 용융기에 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 첨가하되, LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%의 배합비를 이루도록 첨가한 후, 120 ~ 140 ℃의 온도 조건에서 50 ~ 70 rpm으로 5 ~ 15 분 동안 교반하여 조성한 다음 필터처리하여 불연성 수지를 제조하는 단계(S40)를 포함하여 이루어지는 불연성 뿜칠재 제조방법을 제공한다.To the melter, magnesium hydroxide, dispersant, fumed silica as a flame retardant aid, and antioxidant are added, but LDPE/EVA resin 50.0 to 70.0 wt%, magnesium hydroxide 25.0 to 45.0 wt%, and dispersant 0.01 to 2.0 wt. %, fumed silica of a flame retardant auxiliary (0.01 to 2.0 wt%), and an antioxidant (0.01 to 2.0 wt%) were added to achieve a blending ratio of 5 to 70 rpm at a temperature of 120 to 140 °C. It provides a method for producing a non-flammable spray paint comprising the step (S40) of preparing a non-flammable resin by stirring for 15 minutes and then filtering.

본 발명에 따른 불연성 뿜칠재는 높은 불연특성을 가지면서 시공이 간편하고 부착성이 뛰어나다는 특징을 갖는다. 또한 항균 특성과 천연 물질 사용에 따른 사용안전성이 뛰어나다는 장점을 갖는다.The non-flammable spraying material according to the present invention has high non-combustible properties, and is easy to install and has excellent adhesion. In addition, it has the advantage of excellent antibacterial properties and safety in use according to the use of natural substances.

도 1은 본 발명에 따른 불연성 뿜칠재의 제조 공정도.1 is a manufacturing process diagram of a non-flammable spray paint according to the present invention.

이하, 본 발명에 따른 불연성 뿜칠재 및 이의 제조방법에 대한 구체적인 내용에 대해 살펴보도록 한다.Hereinafter, a detailed description of the non-flammable spray coating material and a method of manufacturing the same according to the present invention will be described.

본 발명에 따른 불연성 뿜칠재는 펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%를 혼합하여 100.0 wt%로 조성된 평균입도 200 ~ 1000 mesh의 미분말 혼합물을 800 ℃ ~ 1,200 ℃로 가열하여 팽창시킨 광물 미분말(A) 25.0 ~ 50.0 wt%;The non-flammable spray coating material according to the present invention is a fine powder mixture having an average particle size of 200 to 1000 mesh composed of 100.0 wt% by mixing 1.0 to 50.0 wt% of pearlite, 1.0 to 50.0 wt% of vermiculite, and 1.0 to 50.0 wt% of sepiolite 25.0 to 50.0 wt% of the fine mineral powder (A) expanded by heating at 800° C. to 1,200° C.;

정제수 10.0 ~ 50.0 wt%와, 수산화마그네슘 10.0 ~ 30.0 wt%와, 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 혼합물(B) 40.0 ~ 70.0 wt%;10.0 to 50.0 wt% of purified water, 10.0 to 30.0 wt% of magnesium hydroxide, 10.0 to 30.0 wt% of porous macsumsuk granules, 10.0 to 30.0 wt% of sodium silicate, and 10.0 to 30.0 wt% of urea resin are mixed to form 100.0 wt% Non-combustible mixture (B) 40.0 to 70.0 wt%;

LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 수지(C) 2.0 ~ 5.0 wt%;LDPE/EVA resin 50.0 ~ 70.0 wt%, magnesium hydroxide 25.0 ~ 45.0 wt%, dispersant 0.01 ~ 2.0 wt%, flame retardant fumed silica 0.01 ~ 2.0 wt%, antioxidant 0.01 ~ 2.0 2.0 to 5.0 wt% of a non-combustible resin (C) composed of 100.0 wt% by mixing wt%;

송진(d1) 30.0 ~ 68.0 wt%와, Rosin (d1) 30.0 ~ 68.0 wt% and,

아교와 어교를 1:1 중량비로 혼합한 혼합물(d2) 30.0 ~ 68.0 wt%와, A mixture (d2) 30.0 ~ 68.0 wt% of a mixture of glue and fish glue in a 1:1 weight ratio,

건조시켜 세절한 편백나무 잎을 아세톤에 침적시키되, 편백나무 잎과 70 % 아세톤을 1: 10 ~ 30배의 중량비로 혼합 조성하여 상온에서 4 ~ 6일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 편백나무 추출물과,The dried and shredded cypress leaves are immersed in acetone, but the cypress leaves and 70% acetone are mixed in a weight ratio of 1: 10 to 30 times, and extracted twice at room temperature for 4 to 6 days, and the extract is used with filter paper. Cypress tree extract prepared as a powder by filtering with (filter paper) and drying under reduced pressure,

건조시켜 세절한 약쑥을 에탄올에 침적시키되, 약쑥과 95 % 에탄올을 1 : 8 ~ 12의 중량비로 하여 상온에서 1 ~ 3일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 약쑥 추출물과,Dried fine mugwort was immersed in ethanol, but extracted twice for 1 to 3 days at room temperature with a weight ratio of 1: 8 to 12 of wormwood and 95% ethanol, and the extract was filtered with filter paper. , Wormwood extract prepared as a powder by drying under reduced pressure,

박하와 80 % 에탄올을 1 : 15 ~ 30 중량비로 혼합 조성하여 2 ~ 5 시간 동안 환류추출하고, 추출액을 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 박하추출물을 3:5:2 중량비율로 혼합하여 조성한 항균추출물(d3) 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반 혼합(d1+d2+d3)하여 100.0 wt%로 조성된 천연결합재(D) 2.0 ~ 5.0 wt%;의 혼합(A+B+C+D)으로 조성된다.Mint and 80% ethanol were mixed in a ratio of 1: 15 to 30 and extracted under reflux for 2 to 5 hours, and the extract was filtered with filter paper and dried under reduced pressure to prepare a powdered peppermint extract. A natural binder composed of 100.0 wt% by stirring and mixing (d1+d2+d3) 0.1 to 2.0 wt% of the antibacterial extract (d3) prepared by mixing at a weight ratio of 5:2 for 20 to 50 minutes at 2,000 to 3,000 rpm ( D) 2.0 ~ 5.0 wt%; It is composed of a mixture (A+B+C+D).

상기 광물 미분말은 재질 특성상 불연성과 높은 단열성을 갖는다. 이와 같은 광물 미분말의 사용량이 25.0 wt% 미만인 경우에는 광물 미분말에 의한 불연, 단열 기능 향상이 제한적일 수 있고, 50.0 wt%를 초과하게 되는 경우에는 뿜칠재로서의 기능성이 떨어져 시공의 어려움이 있을 수 있으므로, 상기 광물 미분말의 사용량은 불연성 뿜칠재의 전체 중량에 대해 25.0 ~ 50.0 wt%의 범위 내로 한정하는 것이 바람직하다.The fine mineral powder has non-flammability and high thermal insulation properties in terms of material properties. If the amount of such fine mineral powder is less than 25.0 wt%, the improvement of non-flammable and thermal insulation function due to the fine mineral powder may be limited, and if it exceeds 50.0 wt%, the functionality as a spray paint may be poor and construction may be difficult. The amount of the fine mineral powder is preferably limited within the range of 25.0 to 50.0 wt% based on the total weight of the non-flammable spray coating material.

상기 불연성 혼합물(B)은 뿜칠재의 불연성을 갖는 혼합물로서, 정제수 10.0 ~ 50.0 wt%와, 수산화마그네슘 10.0 ~ 30.0 wt%와, 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%의 혼합으로 조성된다.The non-flammable mixture (B) is a mixture having non-flammability of spray paint, purified water 10.0 to 50.0 wt%, magnesium hydroxide 10.0 to 30.0 wt%, porous macsumsuk granules 10.0 to 30.0 wt%, sodium silicate 10.0 to 30.0 wt% , It is composed of 10.0 ~ 30.0 wt% of urea resin.

상기 수산화마그네슘은 무기계 난연제로서, 열분해 온도가 높고 탈수 반응에 의해 난연 효과를 갖는다. 수산화 알루미늄의 단점인 낮은 탈수개시온도에 비해 수산화마그네슘은 분해개시온도가 250 ℃ 이상으로 안정적이다. 수산화마그네슘의 연소가스 억제 및 난연 메커니즘은 다음과 같다.The magnesium hydroxide, as an inorganic flame retardant, has a high thermal decomposition temperature and has a flame retardant effect by a dehydration reaction. Compared to the low dehydration initiation temperature, which is a disadvantage of aluminum hydroxide, magnesium hydroxide has a stable decomposition initiation temperature of 250 ℃ or higher. The combustion gas suppression and flame retardant mechanisms of magnesium hydroxide are as follows.

Mg(OH)2 ---> MgO + H2O - 187 cal/g(340~430℃)Mg(OH) 2 ---> MgO + H 2 O-187 cal/g (340~430℃)

상기 수산화마그네슘의 사용량이 10.0 wt% 미만인 경우에는 난연 특성의 저하 우려가 있고, 30.0 wt%를 초과하게 되는 경우에는 난연 특성의 향상 정도가 미미하여 무의미하므로, 상기 수산화마그네슘의 사용량은 불연성 혼합물의 전체 중량에 대해 10.0 ~ 30.0 wt%의 범위 내로 한정하는 것이 바람직하다.If the amount of magnesium hydroxide is less than 10.0 wt%, there is a risk of deterioration of the flame retardant property, and if it exceeds 30.0 wt%, the degree of improvement of the flame retardant property is insignificant and therefore insignificant, the amount of magnesium hydroxide used is the total weight of the non-combustible mixture It is preferable to limit it within the range of 10.0 to 30.0 wt% with respect to.

상기 다공질의 맥섬석 과립은 맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 과립화혼합물을 얻는 발포제를 혼합하고, 과립화 화합물을 공지의 과립기를 이용하여 80 ~ 120 ㎛ 범위 이내의 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 제조된 것을 사용한다.The porous Macsumsuk granules are pulverized to have an average particle diameter of 30 to 40 µm of Macsumsuk raw stone, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate in the slurry of Macsumsuk powder (CaCO 3 ) or sodium carbonate (Na 2 CO 3 ) or a foaming agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the macsumsuk powder to obtain a granulated mixture And the granulation compound is molded into granules having an average particle diameter within the range of 80 to 120 µm using a known granulator to prepare Macsumsuk granules, and then the Macsumsuk granules are calcined at a temperature range of 1,000 to 1,200°C. Use the prepared one.

상기 다공질의 맥섬석 과립은 인체에 무해한 재료로서, 높은 난연특성과 함께 원적외선과 음이온 방사의 부가 기능을 갖는 것으로서, 그 사용량이 10.0 wt% 미만인 경우에는 맥섬석 과립에 의한 난연기능성의 향상을 기대하기 어렵고, 30.0 wt%를 초과하게 되는 경우에는 필요 이상의 사용으로 인한 단가 상승의 문제가 있어 비경제적이므로, 상기 다공질의 맥섬석 과립의 사용량은 불연성 혼합물의 전체 중량에 대해 10.0 ~ 30.0 wt%의 범위 내로 한정하는 것이 바람직하다.The porous macsumsuk granules are a material harmless to the human body, and have high flame retardant properties and an additional function of radiating far-infrared rays and anions.When the amount is less than 10.0 wt%, it is difficult to expect improvement of the flame retardant function by macsumsuk granules, If it exceeds 30.0 wt%, it is uneconomical to increase the unit price due to use more than necessary, so the amount of the porous macsumsuk granules is limited to within the range of 10.0 to 30.0 wt% based on the total weight of the non-combustible mixture. desirable.

상기 규산소다는 난연성 및 결합력 증진기능을 갖는 것으로서, 그 사용량이 10.0 wt% 미만인 경우에는 난연특성 향상 및 결합력 증진 효과를 기대하기 어렵고, 30.0 wt%를 초과하게 되는 경우에는 필요 이상의 사용으로 무의미하므로, 상기 규산소다의 사용량은 불연성 혼합물의 전체 중량에 대해 10.0 ~ 30.0 wt%의 범위 내로 한정하는 것이 바람직하다.The sodium silicate has a flame retardancy and cohesion enhancing function, and when the amount is less than 10.0 wt%, it is difficult to expect the flame-retardant property improvement and cohesion enhancing effect, and when it exceeds 30.0 wt%, it is meaningless to use more than necessary, The amount of sodium silicate is preferably limited to within the range of 10.0 to 30.0 wt% based on the total weight of the non-flammable mixture.

상기 요소수지는 내열성 증진을 위해 사용되는 것으로서, 그 사용량이 10.0 wt% 미만인 경우에는 내열성 증진효과를 기대하기 어렵고, 30.0 wt%를 초과하게 되는 경우에는 필요이상의 사용으로 비경제적이므로, 상기 요소수지의 사용량은 불연성 혼합물의 전체 중량에 대해 10.0 ~ 30.0 wt%의 범위 내로 한정하는 것이 바람직하다.The urea resin is used to improve heat resistance, and when the amount of the urea resin is less than 10.0 wt%, it is difficult to expect a heat resistance improvement effect, and when it exceeds 30.0 wt%, it is uneconomical to use more than necessary. The amount used is preferably limited to within the range of 10.0 to 30.0 wt% based on the total weight of the non-flammable mixture.

상기 불연성 혼합물(B)의 구체적인 배합예는 다음의 표 1과 같다.Specific mixing examples of the non-flammable mixture (B) are shown in Table 1 below.

배합예 1Formulation example 1 배합예 2Formulation example 2 배합예 3Formulation example 3 배합예 4Formulation Example 4 배합예 5Formulation Example 5 정제수Purified water 15.0 wt%
15.0 wt%
20.0 wt%20.0 wt% 25.0 wt%25.0 wt% 25.0 wt%25.0 wt% 32.0 wt%32.0 wt%
수산화
마그네슘
Hydration
magnesium
25.0 wt%25.0 wt% 20.0 wt%20.0 wt% 12.0 wt%12.0 wt% 20.0 wt%20.0 wt% 10.0 wt%10.0 wt%
맥섬석 과립Macsumstone granules 30.0 wt%30.0 wt% 30.0 wt%30.0 wt% 33.0 wt%33.0 wt% 25.0 wt%25.0 wt% 28.0 wt%28.0 wt% 규산소다Sodium silicate 20.0 wt%20.0 wt% 20.0 wt%20.0 wt% 20.0 wt%20.0 wt% 20.0 wt%20.0 wt% 20.0 wt%20.0 wt% 요소수지Urea resin 10.0 wt%10.0 wt% 10.0 wt%10.0 wt% 10.0 wt%10.0 wt% 10.0 wt%10.0 wt% 10.0 wt%10.0 wt% 합 계Sum 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt%

상기 불연성 수지는 불연특성을 갖는 수지로서, LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%의 혼합으로 조성된다.The non-combustible resin is a resin having non-combustible properties, LDPE/EVA resin 50.0 to 70.0 wt%, magnesium hydroxide 25.0 to 45.0 wt%, dispersant 0.01 to 2.0 wt%, and fumed silica 0.01 of a flame retardant aid. It is composed of a mixture of ~ 2.0 wt% and 0.01 ~ 2.0 wt% of an antioxidant.

상기 LDPE/EVA 수지는 LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 융용기에 투입한 후 120 ~ 180 에서 3 ~ 7 분 동안 용융혼합하여 조성된 것을 사용한다.The LDPE/EVA resin is formulated by adding 40.0 to 60.0 wt% of low density polyethylene (LDPE) and 40.0 to 60.0 wt% of polyethyleneco-vinylacetate (EVA) to a melting vessel and then melt-mixing at 120 to 180 for 3 to 7 minutes. Use it.

상기 LDPE/EVA 수지의 사용량이 40.0 wt% 미만인 경우에는 성형성이 떨어지고, 70.0 wt%를 초과하게 되는 경우에는 상대적으로 다른 성분들의 함량이 줄어들어 내구성, 난연성 등의 물리, 화학적 특성 저하 우려가 있으므로, 상기 LDPE/EVA 수지의 사용량은 불연성 수지의 전체 중량에 대해 50.0 ~ 70.0 wt%의 범위 내로 한정하는 것이 바람직하다.If the amount of LDPE/EVA resin is less than 40.0 wt%, the moldability is deteriorated, and if it exceeds 70.0 wt%, the content of other components is relatively reduced, so there is a concern that physical and chemical properties such as durability and flame retardancy are deteriorated. The LDPE/EVA resin is preferably used in a range of 50.0 to 70.0 wt% based on the total weight of the non-flammable resin.

상기 수산화마그네슘은 앞서 살펴본 바와 같이 무기계 난연제로 사용되는 것으로서, 그 사용량이 25.0 wt% 미만인 경우에는 난연 특성의 향상을 기대하기 어렵고, 45.0 wt%를 초과하게 되는 경우에는 전체적인 성분 조성의 최적화를 이루기 어려움으로, 상기 수산화마그네슘의 사용량은 불연성 수지의 전체 중량에 대해 25.0 ~ 45.0 wt%의 범위 내로 한정하는 것이 바람직하다.As described above, the magnesium hydroxide is used as an inorganic flame retardant, and when the amount is less than 25.0 wt%, it is difficult to expect improvement of flame retardant properties, and when it exceeds 45.0 wt%, it is difficult to optimize the overall composition of the composition. As such, the amount of magnesium hydroxide is preferably limited to within the range of 25.0 to 45.0 wt% based on the total weight of the non-combustible resin.

상기 분산제는 모노알킬 황산염, 알킬폴리옥시에틸렌황산염, 알킬 벤젠 술폰산염 또는 모노알킬인산염과의 음이온성 계면활성제; 모노알킬트리메틸암모늄염, 디알킬디메틸암모늄염 또는 알킬벤질메틸암모늄염의 양이온성 계면활성제, 알킬설포베타인 또는 알킬카르복시베타인의 양쪽성 이온 계면활성제; 또는 폴리옥시에틸렌알킬에테르, 지방산 솔비탄에스테르, 지방산 디에탄올아민, 또는 알킬모노글리세릴에테르의 비이온성 계면활성제 중 선택되는 것을 사용한다.The dispersant may include an anionic surfactant with monoalkyl sulfate, alkyl polyoxyethylene sulfate, alkyl benzene sulfonate or monoalkyl phosphate; Cationic surfactants of monoalkyltrimethylammonium salts, dialkyldimethylammonium salts or alkylbenzylmethylammonium salts, amphoteric surfactants of alkylsulfobetaine or alkylcarboxybetaine; Or a nonionic surfactant of polyoxyethylene alkyl ether, fatty acid sorbitan ester, fatty acid diethanolamine, or alkyl monoglyceryl ether is used.

상기 분산제의 사용량이 0.01 wt% 미만인 경우에는 분산성이 떨어지고, 2.0 wt%를 초과하게 되는 경우에는 분산성에 미치는 영향의 변화가 없어 무의미하므로, 상기 분산제의 사용량은 불연성 수지의 전체 중량에 대해 0.01 ~ 2.0 wt%의 범위 내로 한정하는 것이 바람직하다.When the amount of the dispersant is less than 0.01 wt%, the dispersibility decreases, and when it exceeds 2.0 wt%, there is no change in the effect on the dispersibility, so the amount of the dispersant is 0.01 to about the total weight of the non-flammable resin. It is preferable to limit it within the range of 2.0 wt%.

상기 난연보조제의 흄드실리카(Fumed silica)는 보조제로 사용되어 난연특성을 더욱 향상시키는 역할을 하는 것으로서, 그 사용량이 0.01 wt% 미만인 경우에는 난연특성 향상의 기능성을 발휘하기 어렵고, 2.0 wt%를 초과하게 되는 경우에는 필요 이상의 사용으로 무의미하므로, 상기 난연보조제의 사용량은 불연성 수지의 전체 중량에 대해 0.01 ~ 2.0 wt%의 범위 내로 한정하는 것이 바람직하다.The fumed silica of the flame retardant auxiliary is used as an auxiliary and serves to further improve the flame retardant properties.If the amount is less than 0.01 wt%, it is difficult to exhibit the functionality of improving flame retardancy, and 2.0 wt% is If it exceeds, it is meaningless to use more than necessary, and therefore, the amount of the flame retardant aid is preferably limited to within the range of 0.01 to 2.0 wt% based on the total weight of the non-combustible resin.

상기 산화방지제는 플라스틱이 공기와 반응하여 쉽게 산화반응을 일으키는 것을 억제하는 것으로서, 페놀계, 아민계, Phosphite 계 또는 Thioester 계 중에서 선택하여 사용한다.The antioxidant is used to inhibit plastic from reacting with air to easily cause an oxidation reaction, and is selected from phenol-based, amine-based, Phosphite-based, or Thioester-based.

더욱 구체적으로는, Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3,5-di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane 또는 Alkylester phosphite 중 선택되는 것을 사용한다.More specifically, Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3, 5-di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane or Alkylester Use selected phosphite.

상기 산화방지제의 사용량이 0.01 wt% 미만인 경우에는 산화방지의 기능을 제대로 발휘하기 어렵기 때문에 상기 산화방지제의 사용량은 불연성 수지의 전체 중량에 대해 0.01 ~ 2.0 wt%의 범위 내로 한정하는 것이 바람직하다.When the amount of the antioxidant is less than 0.01 wt%, it is difficult to properly exhibit the antioxidant function, so the amount of the antioxidant is preferably limited to within the range of 0.01 to 2.0 wt% based on the total weight of the non-combustible resin.

상기 불연성 수지(C)의 구체적인 배합예는 다음의 표 2와 같다.Specific mixing examples of the non-flammable resin (C) are shown in Table 2 below.

배합예 1Formulation example 1 배합예 2Formulation example 2 배합예 3Formulation example 3 배합예 4Formulation Example 4 배합예 5Formulation Example 5 LDPE/EVA 수지LDPE/EVA resin 52.0 wt%52.0 wt% 58.5 wt%58.5 wt% 60.0 wt%60.0 wt% 65.0 wt%65.0 wt% 70.0 wt%70.0 wt% 수산화
마그네슘
Hydration
magnesium
45.0 wt%45.0 wt% 40.0 wt%40.0 wt% 38.5 wt%38.5 wt% 33.5 wt%33.5 wt% 29.4 wt%29.4 wt%
디알킬디메틸암모늄염Dialkyldimethylammonium salt 1.0 wt%1.0 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.2 wt%0.2 wt% 흄드실리카Fumed silica 1.0 wt%1.0 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.2 wt%0.2 wt% Tris(2.4-di-t-butylphenyl)-phosphiteTris(2.4-di-t-butylphenyl)-phosphite 1.0 wt%1.0 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.5 wt%0.5 wt% 0.2 wt%0.2 wt% 합 계Sum 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt%

상기 천연결합재는 송진(d1) 30.0 ~ 68.0 wt%와, The natural binder is 30.0 ~ 68.0 wt% of rosin (d1),

아교와 어교를 1:1 중량비로 혼합한 혼합물(d2) 30.0 ~ 68.0 wt%와, A mixture (d2) 30.0 ~ 68.0 wt% of a mixture of glue and fish glue in a 1:1 weight ratio,

건조시켜 세절한 편백나무 잎을 아세톤에 침적시키되, 편백나무 잎과 70 % 아세톤을 1: 10 ~ 30배의 중량비로 혼합 조성하여 상온에서 4 ~ 6일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 편백나무 추출물과,The dried and shredded cypress leaves are immersed in acetone, but the cypress leaves and 70% acetone are mixed in a weight ratio of 1: 10 to 30 times, and extracted twice at room temperature for 4 to 6 days, and the extract is used with filter paper. Cypress tree extract prepared as a powder by filtering with (filter paper) and drying under reduced pressure,

건조시켜 세절한 약쑥을 에탄올에 침적시키되, 약쑥과 95 % 에탄올을 1 : 8 ~ 12의 중량비로 하여 상온에서 1 ~ 3일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 약쑥 추출물과,Dried fine mugwort was immersed in ethanol, but extracted twice for 1 to 3 days at room temperature with a weight ratio of 1: 8 to 12 of wormwood and 95% ethanol, and the extract was filtered with filter paper. , Wormwood extract prepared as a powder by drying under reduced pressure,

박하와 80 % 에탄올을 1 : 15 ~ 30 중량비로 혼합 조성하여 2 ~ 5 시간 동안 환류추출하고, 추출액을 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 박하추출물을 3:5:2 중량비율로 혼합하여 조성한 항균추출물(d3) 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반하여 혼합(d1+d2+d3)함으로써 조성된다.Mint and 80% ethanol were mixed in a ratio of 1: 15 to 30 and extracted under reflux for 2 to 5 hours, and the extract was filtered with filter paper and dried under reduced pressure to prepare a powdered peppermint extract. It is formulated by mixing (d1+d2+d3) 0.1 to 2.0 wt% of the antibacterial extract (d3) prepared by mixing at a weight ratio of 5:2 and stirring at 2,000 to 3,000 rpm for 20 to 50 minutes.

상기 천연결합재(D)의 구체적인 배합예는 다음의 표 3과 같다.Specific mixing examples of the natural binder (D) are shown in Table 3 below.

배합예 1Formulation example 1 배합예 2Formulation example 2 배합예 3Formulation example 3 배합예Mixing example 배합예5Mixing Example 5 송진Rosin 55.0 wt%55.0 wt% 46.0 wt%46.0 wt% 47.0 wt%47.0 wt% 48.0 wt%48.0 wt% 49.0 wt%49.0 wt% 아교/어교
혼합물
Glue / language school
mixture
44.5 wt%44.5 wt% 53.0 wt%53.0 wt% 51.5 wt%51.5 wt% 51.2 wt%51.2 wt% 50.8 wt%50.8 wt%
항균추출물Antibacterial extract 0.5 wt%0.5 wt% 1.0 wt%1.0 wt% 1.5 wt%1.5 wt% 0.8 wt%0.8 wt% 0.2 wt%0.2 wt% 합 계Sum 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt%

이하, 상기 제시된 불연성 뿜칠재의 제조방법에 대해 살펴보도록 한다.Hereinafter, a method of manufacturing the non-flammable spray coating material presented above will be described.

도 1에 도시된 바와 같이, 본 발명에 따른 불연성 뿜칠재 제조방법은 펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%의 혼합으로 조성된 팽창성 광물을 200 ~ 1000 mesh로 분쇄한 후 800 ℃ ~ 1,200 ℃로 가열, 팽창시켜 광물 미분말을 제조하는 단계(S10)와,As shown in Figure 1, the method for producing a non-flammable spray paint according to the present invention is an expandable mineral composed of a mixture of 1.0 to 50.0 wt% perlite, 1.0 to 50.0 wt% vermiculite, and 1.0 to 50.0 wt% sepiolite. The step (S10) of preparing a fine mineral powder by pulverizing into 200 to 1000 mesh and heating and expanding at 800 to 1,200 °C, and

맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 혼합물을 조성하고, 상기 혼합물을 과립기를 이용하여 80 ~ 120 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 다공질의 맥섬석 과립을 제조하는 단계(S20)와,The raw Macsumsuk stone is pulverized to have an average particle diameter of 30 to 40 µm, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate (CaCO 3 ) or sodium carbonate in the slurry of Macsumsuk powder (Na 2 CO 3 ) or a blowing agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the macsumsuk powder to form a mixture, and the mixture is used in a granulator. After forming the Macsumsuk granules by molding into granules having an average particle diameter of 80 to 120 μm, the Macsumsuk granules are calcined at a temperature range of 1,000 to 1,200° C. to prepare porous Macsumsuk granules (S20),

상기 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 정제수 10.0 ~ 50.0 wt%, 수산화마그네슘 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 불연성 혼합물을 제조하는 단계(S30)와,A step of mixing the porous macsumsuk granules 10.0 to 30.0 wt%, purified water 10.0 to 50.0 wt%, magnesium hydroxide 10.0 to 30.0 wt%, sodium silicate 10.0 to 30.0 wt%, and urea resin 10.0 to 30.0 wt% to prepare a non-combustible mixture (S30) Wow,

LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 융용기에 투입한 후 120 ~ 180 에서 3 ~ 7 분 동안 용융혼합하여 LDPE/EVA 수지를 조성하고, LDPE (low density polyethylene) 40.0 ~ 60.0 wt% and EVA (polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt% were added to the melting machine, and then melt-mixed at 120 ~ 180 for 3 ~ 7 minutes to form LDPE/EVA resin,

상기 용융기에 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 첨가하되, LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%의 배합비를 이루도록 첨가한 후, 120 ~ 140 ℃의 온도 조건에서 50 ~ 70 rpm으로 5 ~ 15 분 동안 교반하여 조성한 다음 필터처리하여 불연성 수지를 제조하는 단계(S40)와,To the melter, magnesium hydroxide, dispersant, fumed silica as a flame retardant aid, and antioxidant are added, but LDPE/EVA resin 50.0 to 70.0 wt%, magnesium hydroxide 25.0 to 45.0 wt%, and dispersant 0.01 to 2.0 wt. %, fumed silica of a flame retardant auxiliary (0.01 to 2.0 wt%), and an antioxidant (0.01 to 2.0 wt%) were added to achieve a blending ratio of 5 to 70 rpm at a temperature of 120 to 140 °C. Stirring for 15 minutes to prepare the composition and then filtering to prepare a non-combustible resin (S40),

송진 30.0 ~ 68.0 wt%와, 아교와 어교를 1:1 중량비로 혼합한 혼합물 30.0 ~ 68.0 wt%와, 편백나무 추출물, 약쑥 추출물 및 박하추출물을 3:5:2 중량비로 혼합 조성한 항균추출물 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반하여 천연결합재를 제조하는 단계(S50)와,30.0 ~ 68.0 wt% of rosin, 30.0 ~ 68.0 wt% of a mixture of 1: 1 weight ratio of glue and fish, and 0.1 ~ 0.1 ~ of an antibacterial extract composed of cypress extract, wormwood extract, and mint extract in a 3:5:2 weight ratio A step (S50) of preparing a natural binder by stirring 2.0 wt% at 2,000 to 3,000 rpm for 20 to 50 minutes,

상기 광물 미분말(a) 25.0 ~ 50.0 wt%; 불연성 혼합물(b) 40.0 ~ 70.0 wt%; 불연성 수지(c) 2.0 ~ 5.0 wt%; 천연결합재(d) 2.0 ~ 5.0 wt%;를 혼합하여 불연성 뿜칠재를 제조하는 단계(S60)를 포함하여 이루어진다.The mineral fine powder (a) 25.0 ~ 50.0 wt%; Incombustible mixture (b) 40.0 to 70.0 wt%; 2.0 to 5.0 wt% of non-combustible resin (c); A natural binder (d) 2.0 ~ 5.0 wt%; comprises a step (S60) of preparing a non-flammable spray paint by mixing.

이하, 각 단계별 기술구성에 대해 구체적으로 살펴보도록 한다.Hereinafter, the technical configuration for each step will be described in detail.

< 광물 미분말 제조 단계(S10) ><Mineral fine powder manufacturing step (S10)>

본 단계(S10)는 광물 미분말을 제조하는 단계로서,This step (S10) is a step of preparing a fine mineral powder,

펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%의 혼합으로 조성된 평균입도 200 ~ 1000 mesh의 미분말 혼합물을 800 ℃ ~ 1,200 ℃로 가열하여 팽창시키는 단계이다.A step of expanding a fine powder mixture with an average particle size of 200 to 1000 mesh composed by mixing 1.0 to 50.0 wt% of pearlite, 1.0 to 50.0 wt% of vermiculite, and 1.0 to 50.0 wt% of sepiolite by heating to 800 ℃ to 1,200 ℃ to be.

더욱 구체적으로는,More specifically,

펄라이트 35.0 wt%와, 버미큘라이트 35.0 wt%와, 세피올라이트 30.0 wt%의 혼합으로 조성된 팽창성 광물 혼합물을 평균입도 300 mesh로 분쇄한 후 800 ℃ ~ 1,200 ℃에서 가열, 팽창시킨 광물 미분말을 사용한다.An expandable mineral mixture composed of a mixture of 35.0 wt% perlite, 35.0 wt% vermiculite, and 30.0 wt% sepiolite is pulverized to an average particle size of 300 mesh, and then heated and expanded at 800°C to 1,200°C. .

< 다공질 맥섬석 과립 제조 단계(S20) ><Porous Macsumsuk granules manufacturing step (S20)>

본 단계(S20)는 전 단계(S10)와는 별개로 진행되는 단계로서,This step (S20) is a step that proceeds separately from the previous step (S10),

맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 혼합물을 조성하고, 상기 혼합물을 과립기를 이용하여 80 ~ 120 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 다공질의 맥섬석 과립을 제조하는 단계이다.The raw Macsumsuk stone is pulverized to have an average particle diameter of 30 to 40 µm, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate (CaCO 3 ) or sodium carbonate in the slurry of Macsumsuk powder (Na 2 CO 3 ) or a blowing agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the macsumsuk powder to form a mixture, and the mixture is used in a granulator. This is a step of preparing Macsumsuk granules by molding them into granules having an average particle diameter of 80 to 120 µm, and then calcining the Macsumsuk granules at a temperature in the range of 1,000 to 1,200°C to prepare porous Macsumsuk granules.

더욱 구체적으로는 다음의 절차에 따라 맥섬석 과립을 제조한다.More specifically, Macsumsuk granules are prepared according to the following procedure.

1. 맥섬석 원석을 40 ㎛의 평균 입경을 갖도록 분쇄한다.1. Crush the raw Macsumsuk to have an average particle diameter of 40 µm.

2. 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말 슬러리를 제조한다.2. Prepare Macsumsuk powder slurry by mixing so that the weight ratio of water and solid powder is 1:2.

3. 맥섬석 분말 슬러리에 탄산칼슘(CaCO3)을 첨가하되, 맥섬석 분말 슬러리의 고형분 기준으로 0.1 wt%의 양으로 첨가하여 혼합물을 조성한다.3. Calcium carbonate (CaCO 3 ) is added to the Macsumsuk powder slurry, but is added in an amount of 0.1 wt% based on the solid content of the Macsumsuk powder slurry to form a mixture.

4. 혼합물을 과립기를 이용하여 100 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한다.4. The mixture is molded into granules having an average particle diameter of 100 µm using a granulator to prepare Macsumsuk granules.

5. 상기 맥섬석 과립을 1,200 ℃의 온도범위에서 소성하여 다공질의 맥섬석 과립을 제조한다.5. The Macsumsuk granules are calcined in a temperature range of 1,200°C to prepare porous Macsumsuk granules.

< 불연성 혼합물 제조 단계(S30) ><Incombustible mixture manufacturing step (S30)>

본 단계(S30)는 전 단계(S20)에서 제조된 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%과, 정제수 10.0 ~ 50.0 wt%, 수산화마그네슘 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 불연성 혼합물을 제조하는 단계이다. 이때 구체적인 배합비는 앞서 표 1에서 제시한 바와 같다.This step (S30) consists of 10.0 to 30.0 wt% of the porous Macsumsuk granules prepared in the previous step (S20), 10.0 to 50.0 wt% of purified water, 10.0 to 30.0 wt% of magnesium hydroxide, 10.0 to 30.0 wt% of sodium silicate, and urea resin. This is a step of preparing a non-flammable mixture by mixing 10.0 to 30.0 wt%. At this time, the specific mixing ratio is as shown in Table 1 above.

< 불연성 수지 제조 단계(S40) ><Incombustible resin manufacturing step (S40)>

본 단계(S40)는 LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 융용기에 투입한 후 120 ~ 180 에서 3 ~ 7 분 동안 용융혼합하여 LDPE/EVA 수지를 조성하고, In this step (S40), 40.0 to 60.0 wt% of LDPE (low density polyethylene) and 40.0 to 60.0 wt% of EVA (polyethyleneco-vinylacetate) are added to the melter, and then melt-mixed at 120 to 180 for 3 to 7 minutes. To make EVA resin,

상기 용융기에 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 첨가하되, LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%의 배합비를 이루도록 첨가한 후, 120 ~ 140 ℃의 온도 조건에서 50 ~ 70 rpm으로 5 ~ 15 분 동안 교반하여 조성한 다음 필터처리하여 불연성 수지를 제조하는 단계이다. 이때 구체적인 배합비는 앞서 표 2에서 제시한 바와 같다.To the melter, magnesium hydroxide, dispersant, fumed silica as a flame retardant aid, and antioxidant are added, but LDPE/EVA resin 50.0 to 70.0 wt%, magnesium hydroxide 25.0 to 45.0 wt%, and dispersant 0.01 to 2.0 wt. %, fumed silica of a flame retardant auxiliary (0.01 to 2.0 wt%), and an antioxidant (0.01 to 2.0 wt%) were added to achieve a blending ratio of 5 to 70 rpm at a temperature of 120 to 140 °C. The composition is stirred for 15 minutes and then filtered to prepare a non-flammable resin. At this time, the specific mixing ratio is as shown in Table 2 above.

상기 분산제는 모노알킬 황산염, 알킬폴리옥시에틸렌황산염, 알킬 벤젠 술폰산염 또는 모노알킬인산염과의 음이온성 계면활성제; 모노알킬트리메틸암모늄염, 디알킬디메틸암모늄염 또는 알킬벤질메틸암모늄염의 양이온성 계면활성제, 알킬설포베타인 또는 알킬카르복시베타인의 양쪽성 이온 계면활성제; 또는 폴리옥시에틸렌알킬에테르, 지방산 솔비탄에스테르, 지방산 디에탄올아민, 또는 알킬모노글리세릴에테르의 비이온성 계면활성제 중 선택되는 것을 사용한다.The dispersant may include an anionic surfactant with monoalkyl sulfate, alkyl polyoxyethylene sulfate, alkyl benzene sulfonate or monoalkyl phosphate; Cationic surfactants of monoalkyltrimethylammonium salts, dialkyldimethylammonium salts or alkylbenzylmethylammonium salts, amphoteric surfactants of alkylsulfobetaine or alkylcarboxybetaine; Or a nonionic surfactant of polyoxyethylene alkyl ether, fatty acid sorbitan ester, fatty acid diethanolamine, or alkyl monoglyceryl ether is used.

상기 산화방지제는 Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3,5-di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane 또는 Alkylester phosphite 중 선택되는 것을 사용한다.The antioxidants are Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3,5 -di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane or Alkylester phosphite Use the one selected from.

< 천연결합재 제조 단계(S50) ><Natural binder manufacturing step (S50)>

본 단계(S50)는 송진 30.0 ~ 68.0 wt%와, 아교와 어교를 1:1 중량비로 혼합한 혼합물 30.0 ~ 68.0 wt%와, 편백나무 추출물, 약쑥 추출물 및 박하추출물을 3:5 2 중량비로 혼합 조성한 항균추출물 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반하여 천연결합재를 제조하는 단계이다.This step (S50) is a mixture of 30.0 to 68.0 wt% of rosin and 30.0 to 68.0 wt% of a mixture of glue and fish at a weight ratio of 1:1, and cypress extract, mugwort extract, and peppermint extract at a ratio of 3:5 to 2 by weight. This is a step of preparing a natural binder by stirring the prepared antibacterial extract 0.1 to 2.0 wt% at 2,000 to 3,000 rpm for 20 to 50 minutes.

더욱 구체적으로는, 상기 표 3의 배합예 2에 따른 배합조성으로서, 송진 46.0 wt%와, 아교와 어교를 1:1 중량비로 혼합한 혼합물 53.0 wt%와, 편백나무 추출물, 약쑥 추출물 및 박하추출물을 3:5:2 중량비로 혼합 조성한 항균추출물 1.0 wt%를 2,500 rpm으로 30 분 동안 교반하여 천연결합재를 제조한다.More specifically, as the blending composition according to blending example 2 of Table 3, 46.0 wt% of rosin, 53.0 wt% of a mixture of glue and fish glue in a 1:1 weight ratio, and cypress tree extract, mugwort extract, and peppermint extract A natural binder was prepared by stirring 1.0 wt% of the antimicrobial extract prepared by mixing at a weight ratio of 3:5:2 at 2,500 rpm for 30 minutes.

< 불연성 뿜칠재 제조 단계(S60) ><Non-flammable spray paint manufacturing step (S60)>

본 단계(S60)는 전 단계들을 통해 제조된 광물 미분말, 불연성 혼합물, 불연성 수지 및 천연결합재를 혼합하여 불연성 뿜칠재를 제조하는 단계로서, 그 구체적인 배합예는 다음의 표 4와 같다.This step (S60) is a step of preparing a non-combustible spray coating material by mixing the fine mineral powder, non-combustible mixture, non-combustible resin and natural binder prepared through the previous steps, and specific examples of the combination are shown in Table 4 below.

배합예 1Formulation example 1 배합예 2Formulation example 2 배합예 3Formulation example 3 배합예 4Formulation Example 4 배합예 5Formulation Example 5 광물 미분말Mineral fine powder 53.0 wt%53.0 wt% 43.0 wt%43.0 wt% 38.0 wt%38.0 wt% 33.0 wt%33.0 wt% 25.0 wt%25.0 wt% 불연성 혼합물Non-flammable mixture 40.0 wt%40.0 wt% 50.0 wt%50.0 wt% 55.0 wt%55.0 wt% 60.0 wt%60.0 wt% 68.0 wt%68.0 wt% 불연성 수지Non-flammable resin 3.0 wt%3.0 wt% 3.0 wt%3.0 wt% 3.0 wt%3.0 wt% 3.0 wt%3.0 wt% 3.0 wt%3.0 wt% 천연결합재Natural binder 4.0 wt%4.0 wt% 4.0 wt%4.0 wt% 4.0 wt%4.0 wt% 4.0 wt%4.0 wt% 4.0 wt%4.0 wt% 합 계Sum 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt% 100.0 wt%100.0 wt%

< 불연성 뿜칠재의 불연성 측정 ><Measurement of non-flammability of non-flammable spray coating material>

본 발명에 따른 불연성 뿜칠재에 대한 불연성을 측정하였다.The non-flammability of the non-flammable spray coating material according to the present invention was measured.

불연성 테스크는 건축내장재로 사용되고 있는 합판의 외면을 전체적으로 뿜칠하여 불연성 판넬을 제조한 후, 불연성 테스트를 하였다.In the non-combustible task, a non-combustible panel was manufactured by spraying the entire outer surface of the plywood used as a building interior material, followed by a non-combustible test.

화염을 상기 불연성 판넬에 불이 붙을 때까지 가하여 시료에 불이 붙지 않거나 3분 아내에 불이 붙어 탄화된 길이가 짧을 경우 불완전 연소로 본다. 이때 산소농도를 변화시키면서 연소여부를 측정하였으며 30 %에서부터 산소농도를 올리면서 착화여부를 확인하였다. 산소농도를 90 %까지 증가시켰으나 본 발명에 따른 불연성 판넬에서는 연소가 일어나지 않았다.If a flame is applied until the non-flammable panel is ignited and the sample does not catch fire, or if the length of carbonization is short due to a fire for 3 minutes, it is regarded as incomplete combustion. At this time, the combustion was measured while changing the oxygen concentration, and the ignition was confirmed by increasing the oxygen concentration from 30%. Although the oxygen concentration was increased to 90%, combustion did not occur in the non-combustible panel according to the present invention.

이로써 본 발명에 따른 불연성 뿜칠재의 불연성이 매우 뛰어남을 확인할 수 있었다.As a result, it was confirmed that the non-flammability of the non-flammable spray coating material according to the present invention was very excellent.

본 발명에 따른 불연성 뿜칠재는 시공이 간편하고 부착성이 뛰어나며, 난연성이 뛰어나 화재 등에 대한 안전성이 뛰어나다는 장점을 갖는 것으로서 산업상 이용가능성이 크다.The non-flammable spraying material according to the present invention has the advantage of being easy to install, excellent adhesion, excellent flame retardancy, and excellent safety against fire, and has great industrial applicability.

Claims (5)

펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%를 혼합하여 100.0 wt%로 조성된 평균입도 200 ~ 1000 mesh의 미분말 혼합물을 800 ℃ ~ 1,200 ℃로 가열하여 팽창시킨 광물 미분말(A) 25.0 ~ 50.0 wt%;
정제수 10.0 ~ 50.0 wt%와, 수산화마그네슘 10.0 ~ 30.0 wt%와, 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 혼합물(B) 40.0 ~ 70.0 wt%;
LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%를 혼합하여 100.0 wt%로 조성된 불연성 수지(C) 2.0 ~ 5.0 wt%;
송진(d1) 30.0 ~ 68.0 wt%와,
아교와 어교를 1:1 중량비로 혼합한 혼합물(d2) 30.0 ~ 68.0 wt%와,
건조시켜 세절한 편백나무 잎을 아세톤에 침적시키되, 편백나무 잎과 70 % 아세톤을 1: 10 ~ 30배의 중량비로 혼합 조성하여 상온에서 4 ~ 6일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 편백나무 추출물과,
건조시켜 세절한 약쑥을 에탄올에 침적시키되, 약쑥과 95 % 에탄올을 1 : 8 ~ 12의 중량비로 하여 상온에서 1 ~ 3일 동안 2회 반복추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 약쑥 추출물과,
박하와 80 % 에탄올을 1 : 15 ~ 30 중량비로 혼합 조성하여 2 ~ 5 시간 동안 환류추출하고, 추출액을 필터페이퍼(filter paper)로 여과하고, 감압건조하여 파우더로 제조된 박하추출물을 3:5:2 중량비율로 혼합하여 조성한 항균추출물(d3) 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반 혼합(d1+d2+d3)하여 100.0 wt%로 조성된 천연결합재(D) 2.0 ~ 5.0 wt%;의 혼합(A+B+C+D)으로 조성되는 것임을 특징으로 하는 불연성 뿜칠재.
Perlite 1.0 ~ 50.0 wt%, vermiculite 1.0 ~ 50.0 wt%, and sepiolite 1.0 ~ 50.0 wt% are mixed to heat a fine powder mixture with an average particle size of 200 ~ 1000 mesh composed of 100.0 wt% to 800 ℃ ~ 1,200 ℃ Fine mineral powder (A) expanded by 25.0 to 50.0 wt%;
10.0 to 50.0 wt% of purified water, 10.0 to 30.0 wt% of magnesium hydroxide, 10.0 to 30.0 wt% of porous macsumsuk granules, 10.0 to 30.0 wt% of sodium silicate, and 10.0 to 30.0 wt% of urea resin are mixed to form 100.0 wt% Non-combustible mixture (B) 40.0 to 70.0 wt%;
LDPE/EVA resin 50.0 ~ 70.0 wt%, magnesium hydroxide 25.0 ~ 45.0 wt%, dispersant 0.01 ~ 2.0 wt%, flame retardant fumed silica 0.01 ~ 2.0 wt%, antioxidant 0.01 ~ 2.0 2.0 to 5.0 wt% of a non-combustible resin (C) composed of 100.0 wt% by mixing wt%;
Rosin (d1) 30.0 ~ 68.0 wt%,
A mixture (d2) 30.0 ~ 68.0 wt% of a mixture of glue and fish glue in a 1:1 weight ratio,
The dried and shredded cypress leaves are immersed in acetone, but the cypress leaves and 70% acetone are mixed in a weight ratio of 1: 10 to 30 times, and extracted twice at room temperature for 4 to 6 days, and the extract is used with filter paper. Cypress tree extract prepared as a powder by filtering with (filter paper) and drying under reduced pressure,
Dried fine mugwort was immersed in ethanol, but extracted twice for 1 to 3 days at room temperature with a weight ratio of 1: 8 to 12 of wormwood and 95% ethanol, and the extract was filtered with filter paper. , Wormwood extract prepared as a powder by drying under reduced pressure,
Peppermint and 80% ethanol were mixed in a ratio of 1: 15 to 30 and extracted under reflux for 2 to 5 hours, and the extract was filtered with filter paper and dried under reduced pressure to obtain a powdered mint extract of 3:5. Natural binder (D) composed of 100.0 wt% by stirring and mixing (d1+d2+d3) 0.1 to 2.0 wt% of the antibacterial extract (d3) formulated by mixing at a ratio of 2 by weight at 2,000 to 3,000 rpm for 20 to 50 minutes (d1+d2+d3) 2.0 ~ 5.0 wt%; Non-flammable spray coating, characterized in that the composition of the mixture (A + B + C + D).
청구항 1에 있어서,
다공질의 맥섬석 과립은 맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 혼합물을 조성하고, 상기 혼합물을 과립기를 이용하여 80 ~ 120 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 제조된 것임을 특징으로 하는 불연성 뿜칠재.
The method according to claim 1,
Porous Macsumsuk granules are pulverized to have an average particle diameter of 30 to 40 µm, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate ( CaCO 3 ) or sodium carbonate (Na 2 CO 3 ) or a blowing agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the Macsumsuk powder to form a mixture, and the mixture A non-flammable spray coating, characterized in that it is manufactured by molding the Macsumsuk granules into granules having an average particle diameter of 80 to 120 μm using a granulator, and then calcining the Macsumsuk granules at a temperature range of 1,000 to 1,200°C.
청구항 1에 있어서,
LDPE/EVA 수지는 LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 융용기에 투입한 후 120℃~180℃ 에서 3 ~ 7 분 동안 용융혼합하여 조성된 것임을 특징으로 하는 불연성 뿜칠재.
The method according to claim 1,
LDPE/EVA resin is composed by adding 40.0 to 60.0 wt% of LDPE (low density polyethylene) and 40.0 to 60.0 wt% of EVA (polyethyleneco-vinylacetate) into a melting vessel and then melt-mixing at 120℃ to 180℃ for 3 to 7 minutes. Non-flammable spray painting material characterized by being made.
청구항 1에 있어서,
산화방지제는 Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3,5-di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane 또는 Alkylester phosphite 중 선택되는 어느 1종 또는 2종 이상인 것임을 특징으로 하는 불연성 뿜칠재.
The method according to claim 1,
Antioxidants are Tris(2.4-di-t-butylphenyl)-phosphite, Bis(2.4-di-t-butyl), 2.2-Methylenebis(4-methyl-6-t-butylphenol), Pentaerythritol diphosphite, Octadecyl 3,5- di-t-butyl-4-hydroxhydrocinnamate, 2.6-di-t-Butyl-4-methylphenol, Tetrakis[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane or Alkylester phosphite Non-flammable spray coating, characterized in that any one or two or more selected.
펄라이트 1.0 ~ 50.0 wt%와, 버미큘라이트 1.0 ~ 50.0 wt%와, 세피올라이트 1.0 ~ 50.0 wt%의 혼합으로 조성된 팽창성 광물을 200 ~ 1000 mesh로 분쇄한 후 800 ℃ ~ 1,200 ℃로 가열, 팽창시켜 광물 미분말을 제조하는 단계(S10)와,
맥섬석 원석을 30 ~ 40 ㎛의 평균 입경을 갖도록 분쇄하고, 물과 고형분 분말의 중량비가 1:2가 되도록 혼합하여 맥섬석 분말의 슬러리를 제조하고, 맥섬석 분말의 슬러리에 탄산칼슘(CaCO3) 또는 탄산나트륨(Na2CO3) 또는 이들의 혼합물로부터 이루어지는 그룹으로부터 선택되는 발포제 분말을 상기 맥섬석 분말의 슬러리의 고형분 기준으로 0.01 ~ 0.1 wt%의 양으로 혼합하여 혼합물을 조성하고, 상기 혼합물을 과립기를 이용하여 80 ~ 120 ㎛ 평균입경의 과립상으로 성형하여 맥섬석 과립을 제조한 후, 상기 맥섬석 과립을 1,000 ~ 1,200 ℃의 온도범위에서 소성하여 다공질의 맥섬석 과립을 제조하는 단계(S20)와,
상기 다공질의 맥섬석 과립 10.0 ~ 30.0 wt%, 정제수 10.0 ~ 50.0 wt%, 수산화마그네슘 10.0 ~ 30.0 wt%, 규산소다 10.0 ~ 30.0 wt%, 요소수지 10.0 ~ 30.0 wt%를 혼합하여 불연성 혼합물을 제조하는 단계(S30)와,
LDPE(Low density polyethylene) 40.0 ~ 60.0 wt%와 EVA(polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt%를 용융기에 투입한 후 120 ~ 180 에서 3 ~ 7 분 동안 용융혼합하여 LDPE/EVA 수지를 조성하고,
상기 용융기에 수산화마그네슘, 분산제, 난연보조제의 흄드실리카(Fumed silica), 산화방지제를 첨가하되, LDPE/EVA 수지 50.0 ~ 70.0 wt%와, 수산화마그네슘 25.0 ~ 45.0 wt%와, 분산제 0.01 ~ 2.0 wt%와, 난연보조제의 흄드실리카(Fumed silica) 0.01 ~ 2.0 wt%와, 산화방지제 0.01 ~ 2.0 wt%의 배합비를 이루도록 첨가한 후, 120 ~ 140 ℃의 온도 조건에서 50 ~ 70 rpm으로 5 ~ 15 분 동안 교반하여 조성한 다음 필터처리하여 불연성 수지를 제조하는 단계(S40)와,
송진 30.0 ~ 68.0 wt%와, 아교와 어교를 1:1 중량비로 혼합한 혼합물 30.0 ~ 68.0 wt%와, 편백나무 추출물, 약쑥 추출물 및 박하추출물을 3:5:2 중량비로 혼합 조성한 항균추출물 0.1 ~ 2.0 wt%를 2,000 ~ 3,000 rpm에서 20 ~ 50 분 동안 교반하여 천연결합재를 제조하는 단계(S50)와,
상기 광물 미분말(a) 25.0 ~ 50.0 wt%; 불연성 혼합물(b) 40.0 ~ 70.0 wt%; 불연성 수지(c) 2.0 ~ 5.0 wt%; 천연결합재(d) 2.0 ~ 5.0 wt%;를 혼합하여 불연성 뿜칠재를 제조하는 단계(S60)를 포함하여 이루어지는 것임을 특징으로 하는 불연성 뿜칠재 제조방법.
An expandable mineral formed by mixing 1.0 to 50.0 wt% of perlite, 1.0 to 50.0 wt% of vermiculite, and 1.0 to 50.0 wt% of sepiolite was pulverized into 200 to 1000 mesh, and then heated and expanded at 800 to 1,200°C. The step of preparing a fine mineral powder (S10),
The raw Macsumsuk stone is pulverized to have an average particle diameter of 30 to 40 µm, and mixed so that the weight ratio of water and solid powder is 1:2 to prepare a slurry of Macsumsuk powder, and calcium carbonate (CaCO 3 ) or sodium carbonate in the slurry of Macsumsuk powder (Na 2 CO 3 ) or a blowing agent powder selected from the group consisting of a mixture thereof is mixed in an amount of 0.01 to 0.1 wt% based on the solid content of the slurry of the macsumsuk powder to form a mixture, and the mixture is used in a granulator. After forming the Macsumsuk granules by molding into granules having an average particle diameter of 80 to 120 μm, the Macsumsuk granules are calcined at a temperature range of 1,000 to 1,200° C. to prepare porous Macsumsuk granules (S20),
A step of mixing the porous macsumsuk granules 10.0 to 30.0 wt%, purified water 10.0 to 50.0 wt%, magnesium hydroxide 10.0 to 30.0 wt%, sodium silicate 10.0 to 30.0 wt%, and urea resin 10.0 to 30.0 wt% to prepare a non-combustible mixture (S30) Wow,
LDPE (low density polyethylene) 40.0 ~ 60.0 wt% and EVA (polyethyleneco-vinylacetate) 40.0 ~ 60.0 wt% were added to the melter and then melted and mixed at 120 to 180 for 3 to 7 minutes to form LDPE/EVA resin,
To the melter, magnesium hydroxide, dispersant, fumed silica as a flame retardant aid, and antioxidant are added, but LDPE/EVA resin 50.0 to 70.0 wt%, magnesium hydroxide 25.0 to 45.0 wt%, and dispersant 0.01 to 2.0 wt. %, fumed silica of a flame retardant auxiliary (0.01 to 2.0 wt%), and an antioxidant (0.01 to 2.0 wt%) were added to achieve a blending ratio of 5 to 70 rpm at a temperature of 120 to 140 °C. Stirring for 15 minutes to prepare the composition and then filtering to prepare a non-combustible resin (S40),
30.0 ~ 68.0 wt% of rosin, 30.0 ~ 68.0 wt% of a mixture of 1: 1 weight ratio of glue and fish, and 0.1 ~ 0.1 ~ of an antibacterial extract composed of cypress extract, wormwood extract, and mint extract in a 3:5:2 weight ratio A step (S50) of preparing a natural binder by stirring 2.0 wt% at 2,000 to 3,000 rpm for 20 to 50 minutes,
The mineral fine powder (a) 25.0 ~ 50.0 wt%; Incombustible mixture (b) 40.0 to 70.0 wt%; 2.0 to 5.0 wt% of non-combustible resin (c); Natural binder (d) 2.0 ~ 5.0 wt%; Non-flammable spray coating method comprising the step (S60) of preparing a non-flammable spray coating material by mixing.
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