KR20200145637A - Method for Manufacture of Deodorant Sanitary Materials - Google Patents

Method for Manufacture of Deodorant Sanitary Materials Download PDF

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KR20200145637A
KR20200145637A KR1020190144095A KR20190144095A KR20200145637A KR 20200145637 A KR20200145637 A KR 20200145637A KR 1020190144095 A KR1020190144095 A KR 1020190144095A KR 20190144095 A KR20190144095 A KR 20190144095A KR 20200145637 A KR20200145637 A KR 20200145637A
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weight
parts
deodorant
extract
mixture
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KR1020190144095A
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Korean (ko)
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KR102267620B1 (en
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김태웅
김영진
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오가닉브릿지 주식회사
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/46Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/511Topsheet, i.e. the permeable cover or layer facing the skin
    • A61F13/51113Topsheet, i.e. the permeable cover or layer facing the skin comprising an additive, e.g. lotion or odour control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F13/511Topsheet, i.e. the permeable cover or layer facing the skin
    • A61F13/51121Topsheet, i.e. the permeable cover or layer facing the skin characterised by the material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/84Accessories, not otherwise provided for, for absorbent pads
    • A61F13/8405Additives, e.g. for odour, disinfectant or pH control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/18Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/40Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing ingredients of undetermined constitution or reaction products thereof, e.g. plant or animal extracts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F2013/51059Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers being sprayed with chemicals
    • A61F2013/51076Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers being sprayed with chemicals with perfumes or odour-masking agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/51Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers
    • A61F2013/5109Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers with odour control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/84Accessories, not otherwise provided for, for absorbent pads
    • A61F13/8405Additives, e.g. for odour, disinfectant or pH control
    • A61F2013/8408Additives, e.g. for odour, disinfectant or pH control with odour control

Abstract

The present invention relates to a deodorant for sanitary materials and, more specifically, to a deodorant, a composition used for manufacturing the same, a method for manufacturing the same, and sanitary materials using the same, wherein the deodorant has excellent deodorizing power and excellent long-term stability of the deodorizing power, and does not cause skin trouble. The deodorant for sanitary materials comprises a ceramic colloid, a plant extracted complex fermented product, floral water, a natural preservative, a binder and a thickener.

Description

위생재용 소취제 제조방법{Method for Manufacture of Deodorant Sanitary Materials}Method for manufacturing deodorant sanitary materials {Method for Manufacture of Deodorant Sanitary Materials}

본 발명은 천연 식물 추출 성분 등을 이용한 위생재용 소취제를 제조하는 방법에 관한 것이다.The present invention relates to a method for producing a deodorant for hygiene products using natural plant extract components.

최근 의료 산업의 발달, 위생 환경의 청결 등으로 인해 인간의 수명이 대폭 길어져 평균 수명이 80세를 넘어, 100세 장수 시대가 현실로 다가오고 있다. 이에 따라 노인들은 자신의 몸이나 의류에서 발생하는 악취를 제거하는데 상당히 노력과 비용을 들이고 있으며, 또한 어린이나 여성, 병원 환자, 생선 등의 어류나 육류를 취급하는 사람들도 같은 고민을 하고 있는 실정이다. 특히 이들이 사용하는 의류, 여성 생리대, 환자나 어린아이의 기저귀 등에 악취가 베면, 의류는 세탁을 하여도 제거되지 않고, 또한 몸에 베인 악취는 목욕을 하여도 그대로 남아 자신은 물론, 가족이나 타인과의 원만한 대인관계를 유지하기 어렵게 되는 원인이 되기도 한다. Due to the recent development of the medical industry and the cleanliness of the hygienic environment, the life expectancy of humans has been greatly extended, and the average life span has exceeded 80, and the era of longevity of 100 years is approaching a reality. Accordingly, the elderly spend considerable effort and expense in removing odors from their bodies or clothing, and also children, women, hospital patients, and people who handle fish or meat such as fish are having the same concerns. . In particular, if the clothes they use, women's sanitary pads, diapers of patients or children, etc. get bad smells, the clothes are not removed even after washing, and the bad odors cut into the body remain even after taking a bath. It can also be a cause of difficulty in maintaining a smooth interpersonal relationship.

이러한 악취를 제거하기 위하여 향수나 방향제를 사용할 경우, 악취가 제거되기 어렵고, 또 제거가 된다 하더라도, 그의 부작용의 폐해가 더 커서 건강에 해악을 끼칠 수도 있다. 이러한 문제를 해결하기 위해 통상, 잦은 세탁, 목욕, 실내 환기 등을 통해 외부로부터의 악취가 유입되는 것을 막고자 하는 소극적 방법이 널리 이용되고 있다. 그러나, 이러한 방법으로는 악취를 제거할 수 없고, 장기간 요하며, 방향제의 경우, LPG와 같은 압축가스를 사용한 제제의 경우, 고온에서 폭발 위험이 있고, 어린이들에게 안전 사고의 위험이 있다. 무엇보다 큰 문제는 방향제는 제2의 환경오염의 원인이 되기도 한다.When perfumes or fragrances are used to remove such odors, it is difficult to remove odors, and even if they are removed, the adverse effects of their side effects are greater and may harm health. In order to solve this problem, a passive method is widely used to prevent the inflow of odors from the outside through frequent washing, bathing, and indoor ventilation. However, such a method cannot remove odor and requires a long period of time. In the case of fragrances, in the case of formulations using compressed gas such as LPG, there is a risk of explosion at high temperatures, and there is a risk of safety accidents to children. The biggest problem of all is that air fresheners can also cause the second environmental pollution.

종래, 소취제로서는 녹차, 천연 식물 또는 그의 추출물 등을 이용한 소취제, 금속, 다공성 물질 등의 광물을 이용한 소취제, 효소나 미생물을 이용한 소취제 등이 다수 개시되어 있다. 특히, 천연 식물이나 그의 추출물을 액상으로 하거나, 또는 탄산칼슘 등의 다공질체에 담지시킨 이용한 발명, 목초액을 색소첨가제와 배합한 소취제, 에센셜 오일과 식물성 폴리페놀을 주성분으로 하는 소취제, 키틴 또는 키토산의 올리고머를 개질시켜 섬유나 필름에 혼합하여 항균 소취작용을 갖는 발명, 아밀라아제, 프로테아제 등의 미생물과 증점체를 함유하는 세정, 소취제, 담자균 균사체 발효산물을 함유하는 소취제, 과산화물과 질산 이온을 함유하는 소취제 광촉매, 광물질의 미분말을 이용한 소취제 등이 특허 발명된 바 있다. Conventionally, as a deodorant, a number of deodorants using green tea, natural plants or extracts thereof, deodorants using minerals such as metals and porous substances, and deodorants using enzymes or microorganisms have been disclosed. In particular, the invention using natural plants or extracts thereof as a liquid or supported on a porous body such as calcium carbonate, a deodorant in which wood vinegar is mixed with a color additive, a deodorant containing essential oils and vegetable polyphenols as main components, chitin or chitosan Invention having antibacterial deodorant effect by modifying oligomer and mixing it with fiber or film, washing containing microorganisms such as amylase and protease and thickener, deodorant, deodorant containing basidiomycete mycelium fermentation product, deodorant containing peroxide and nitrate ions A photocatalyst and a deodorant using fine powders of mineral substances have been patented.

한국 특허등록공보 제10-637922호 (공고일 2006.10.17)Korean Patent Registration Publication No. 10-637922 (announcement date 2006.10.17) 한국 특허등록공보 제10-0798221호 (공고일 2008.01.18)Korean Patent Registration Publication No. 10-0798221 (announcement date 2008.01.18)

본 발명은 피부에 직접 접촉하는 제품 특성상, 인체에 직접 접촉해도 인체에 무해하고 피부 트러블이 없으면서, 소취력이 우수한 위생재용 소취제를 제조할 수 있는 조성물의 최적 조성 및 조성비를 알게 되어 완성한 발명이다. 즉, 본 발명은 위생재용 소취제 제조방법을 제공하는데 그 목적이 있다. The present invention is an invention completed by knowing the optimum composition and composition ratio of a composition capable of producing a deodorant for hygiene materials having excellent deodorizing power while being harmless to the human body and without skin troubles even if it is in direct contact with the human body due to the nature of the product in direct contact with the skin. That is, an object of the present invention is to provide a method for producing a deodorant for hygiene materials.

상술한 과제를 해결하기 위하여 본 발명의 위생재용 소취제 조성물은 세라믹 콜로이드, 식물 추출 복합 발효물, 천연방부제 및 증점제 및 잔량의 플로랄 워터를 포함한다.In order to solve the above problems, the deodorant composition for sanitary materials of the present invention includes a ceramic colloid, a plant-extracted complex fermented product, a natural preservative and a thickener, and a balance of floral water.

또한, 본 발명의 다른 목적은 상기 조성물을 이용한 위생재용 소취제로서, 분말 형태의 위생재용 소취제를 제공하고자 한다.In addition, another object of the present invention is to provide a deodorant for sanitary materials in a powder form as a deodorant for sanitary materials using the composition.

또한, 본 발명의 다른 목적은 위생재용 소취제의 제조방법에 관한 것으로서, 평균입도 세라믹 콜로이드, 식물 추출 복합 발효물, 플로랄 워터, 천연방부제 및 증점제를 혼합하여 혼합물을 준비하는 1단계; 상기 혼합물을 미분쇄 공정을 수행하여 미분쇄물을 수득하는 2단계; 및 상기 미분쇄물을 건조시켜서 분말을 수득하는 3단계;를 포함하는 공정을 수행하여 위생재용 소취제를 제조할 수 있다.In addition, another object of the present invention relates to a method for producing a deodorant for hygiene, comprising: a first step of preparing a mixture by mixing an average particle size ceramic colloid, a plant-extracted complex fermented product, floral water, a natural preservative and a thickener; A second step of obtaining a finely pulverized product by performing a fine pulverization process on the mixture; And a 3 step of drying the finely pulverized material to obtain a powder, thereby preparing a deodorant for sanitary materials.

또한, 본 발명의 또 다른 목적은 상기 위생재용 소취제를 이용한 위생제를 제공하고자 한다.In addition, another object of the present invention is to provide a hygiene agent using the hygiene deodorant.

본 발명의 소취제 조성물로 제조한 소취제는 우수한 소취력을 가지며, 소취력의 장기 안정성이 우수하면서, 피부 트러블을 유발하지 않는 바, 유아용 기저귀, 성잉용 기저귀, 여성용 생리대 등의 위생재로 사용하기에 적합하다.The deodorant prepared with the deodorant composition of the present invention has excellent deodorant power, has excellent long-term stability of the deodorant power, and does not cause skin troubles, so it is suitable for use as hygiene materials such as diapers for infants, diapers for sex, and sanitary napkins for women. Suitable.

도 1은 실시예 1에서 사용한 세라믹 콜로이드를 전자현미경으로 찍은 사진이다.
도 2은 실시예 1에서 제조한 소취제를 찍은 사진이다.
도 3는 제조예 1에서 제조한 위생재용 SAP(Super Absorbent Polymer) 시트를 찍은 사진이다.
1 is a photograph of the ceramic colloid used in Example 1 taken with an electron microscope.
2 is a photograph taken of the deodorant prepared in Example 1.
3 is a photograph taken of a SAP (Super Absorbent Polymer) sheet for sanitary materials prepared in Preparation Example 1.

이하, 본 발명의 위생재용 소취제를 제조하는 방법을 통해 더욱 구체적으로 설명한다.Hereinafter, it will be described in more detail through the method of manufacturing the deodorant for sanitary materials of the present invention.

본 발명의 위생재용 소취제는 세라믹 콜로이드, 식물 추출 복합 발효물, 플로랄 워터, 천연방부제 및 증점제를 혼합하여 혼합물(또는 조성물)을 준비하는 1단계; 상기 혼합물(또는 조성물)을 미분쇄 공정을 수행하여 미분쇄물을 수득하는 2단계; 및 상기 미분쇄물을 건조시켜서 분말(또는 파우더)을 수득하는 3단계;를 포함하는 공정을 수행하여 제조할 수 있다.The first step of preparing a mixture (or composition) by mixing ceramic colloids, plant-extracted complex fermented products, floral water, natural preservatives, and thickeners for the deodorant for sanitary materials of the present invention; A second step of obtaining a finely pulverized product by performing a fine pulverization process on the mixture (or composition); And it can be produced by performing a process comprising a; 3 step of drying the finely pulverized to obtain a powder (or powder).

1단계의 상기 혼합물 성분 중 상기 세라믹 콜로이드는 식물 추출 복합 발효물 및 플로랄 워터 등의 조성에 대한 지지체 내지 담체 역할을 하는 것으로서, 상기 세라믹 콜로이드는 실리카, 제올라이트, 알루미나, 활성탄, 이산화티탄, 벤토나이트, 산화아연 및 이산화티타늄 중에서 선택된 1종 이상을 포함하는 다공성 무기 광물을 사용할 수 있으며, 바람직하게는 이산화아연, 이산화티탄 및 실리카 중에서 선택된 2종 이상을, 더욱 바람직하게는 이산화아연, 이산화티탄 및 실리카를 사용할 수 있다. 그리고, 이산화아연, 이산화티탄 및 실리카를 3종을 혼합하여 사용하는 경우에는 이산화아연 10 ~ 35 중량%, 이산화티탄 분말 10 ~ 20 중량% 및 잔량의 실리카를 혼합하는 것이, 더욱 바람직하게는 이산화아연 20 ~ 30 중량%, 이산화티탄 분말 12 ~ 18 중량% 및 잔량의 실리카를 혼합하여 사용하는 것이 좋다.Among the components of the mixture in step 1, the ceramic colloid serves as a support or carrier for the composition of plant-extracted complex fermented products and floral water, and the ceramic colloid is silica, zeolite, alumina, activated carbon, titanium dioxide, bentonite, and oxidation. Porous inorganic minerals containing at least one selected from zinc and titanium dioxide may be used, preferably at least two selected from zinc dioxide, titanium dioxide and silica, more preferably zinc dioxide, titanium dioxide, and silica. I can. And, when using a mixture of three types of zinc dioxide, titanium dioxide and silica, it is preferable to mix 10 to 35% by weight of zinc dioxide, 10 to 20% by weight of titanium dioxide powder, and the remaining amount of silica, more preferably zinc dioxide. It is preferable to use a mixture of 20 to 30% by weight, 12 to 18% by weight of titanium dioxide powder, and the remaining amount of silica.

그리고, 상기 혼합물 내 세라믹 콜로이드의 함량은 혼합물 전체 중량 중 50 ~ 65 중량%로, 바람직하게는 52 ~ 64 중량%로, 더욱 바람직하게는 56 ~ 64 중량%로 사용하는 것이 좋으며, 이때, 세라믹 콜로이드 함량이 50 중량% 미만이면 담체 역할을 하는 성분이 너무 적어서 소취제 수득률이 낮아져서 제조 경제성이 떨어지는 문제가 있을 수 있고, 그 함량이 65 중량%를 초과하면 오히려 소취제의 소취력이 떨어지는 문제가 있을 수 있으므로 상기 범위 내로 사용하는 것이 좋다. In addition, the content of the ceramic colloid in the mixture is 50 to 65% by weight, preferably 52 to 64% by weight, more preferably 56 to 64% by weight of the total weight of the mixture, and in this case, ceramic colloids If the content is less than 50% by weight, there may be a problem in that the yield of the deodorant is lowered because the component serving as a carrier is too small, and if the content exceeds 65% by weight, there may be a problem that the deodorant power of the deodorant is lowered. It is recommended to use within the above range.

또한, 상기 세라믹 콜로이드는 다공성이라서 그 자체로 소취력이 있으나 적정 크기의 세라믹 콜로이드를 사용하여 식물 추출 복합 발효물 등이 세라믹 콜로이드의 공극에 함침되어 소취력 증대 효과를 꾀할 수 있다. 상기 세라믹 콜로이드는 평균입도 0.1㎛ ~ 2.0㎛인 것이, 바람직하게는 0.2㎛ ~ 1.2㎛인 것이, 더욱 바람직하게는 0.2㎛ ~ 1.0㎛인 것이 좋으며, 세라믹 콜로이드의 평균입도가 0.2㎛ 미만이면 너무 작아서 다른 성분들이 세라믹 콜로이드에 충분하게 담지되지 않아서 얻고자 하는 소취력 증대 효과를 보기 어려울 수 있고, 제조 및 구입이 매우 어려우며, 평균입도가 2㎛를 초과하면 세라믹 콜로이드의 크기가 너무 커서 소취 작용하는 작용 면적이 오히려 작아서 소취력이 떨어지는 문제가 있을 수 있으므로, 상기 범위 내의 크기를 가지도록 세라믹 콜로이드를 미리 분쇄 등을 하여 준비하는 것이 좋다.In addition, since the ceramic colloid is porous, it has a deodorizing power by itself. However, by using a ceramic colloid of an appropriate size, a plant-extracted complex fermentation product or the like is impregnated into the pores of the ceramic colloid, thereby increasing the deodorizing power. The ceramic colloid has an average particle size of 0.1 μm to 2.0 μm, preferably 0.2 μm to 1.2 μm, more preferably 0.2 μm to 1.0 μm, and if the average particle size of the ceramic colloid is less than 0.2 μm, it is too small. Other ingredients are not sufficiently supported in the ceramic colloid, so it may be difficult to see the effect of increasing the desired deodorant. It is very difficult to manufacture and purchase. If the average particle size exceeds 2㎛, the size of the ceramic colloid is too large to act as a deodorant. Since the area is rather small, there may be a problem that the deodorizing power is inferior, so it is preferable to prepare a ceramic colloid by grinding or the like in advance so as to have a size within the above range.

앞서 설명한 바와 같이, 악취 성분은 기상(氣相)이므로 기상 물질이 세라믹 콜로이드와 접촉하여 악취 제거가 가능하나 이는 제한적 기능인 바, 공극에 함침된 다른 성분들과 악취 유발 물질의 접촉을 통한 소취능 향상 효과를 얻을 수 있는 것이다. As described above, since the odor component is in the gas phase, it is possible to remove the odor by contacting the gaseous substance with the ceramic colloid, but this is a limited function, improving the deodorizing ability through contact of other components impregnated in the pores with the odor-causing substance. You can get the effect.

1단계의 상기 혼합물 성분 중 상기 식물 추출 복합 발효물은 세라믹 콜로이드 및/또는 위생재 제조에 사용되는 섬유 등으로 인한 피부 트러블 유발을 방지하면서, 세라믹 콜로이드와 함께 소취력 증대 역할을 하는 것으로서, 식물 추출물을 혼합한 식물 추출 혼합물을 발효 여과물로 발효시켜서 제조한 것이다.Among the components of the mixture in step 1, the plant-extracted complex fermented product prevents skin troubles caused by ceramic colloids and/or fibers used in the manufacture of sanitary materials, and plays a role in increasing deodorant power together with ceramic colloids. It is prepared by fermenting the plant extract mixture mixed with the fermentation filtrate.

상기 식물 추출 혼합물은 병출 추출물, 청호 추출물, 감초 추출물, 님잎 추출물, 컴프리잎 추출물 및 녹차 추출물 포함하며, 바람직하게는 병출 추출물 100 중량부에 대하여, 청호 추출물 60 ~ 100 중량부, 감초 추출물 60 ~ 100 중량부, 님잎 추출물 30 ~ 70 중량부, 컴프리잎 추출물 30 ~ 70 중량부 및 녹차 추출물 15 ~ 50 중량부를 포함하고, 더욱 바람직하게는 병출 추출물 100 중량부에 대하여, 청호 추출물 70 ~ 90 중량부, 감초 추출물 60 ~ 85 중량부, 님잎 추출물 35 ~ 55 중량부, 컴프리잎 추출물 35 ~ 60 중량부 및 녹차 추출물 25 ~ 40 중량부를 포함하는 것이 좋다. 이때, 청호 추출물이 60 중량부 미만이면 손상 피부에 대한 피부 재생 효과가 없을 수 있고, 100 중량부를 초과하면 가격 상승 및 피부 트러블을 오히려 유발하는 문제가 있을 수 있다. 또한, 감초 추출물이 60 중량부 미만이면 성난 피부를 진정시키는 효과가 없을 수 있고, 100 중량부를 초과하면 과량 사용으로 제조비용만 증가 하는 문제가 있을 수 있다. 또한, 상기 님잎 추출물이 30 중량부 미만이면 피부의 가려움증 및 염증 완화 효과가 없을 수 있고, 70 중량부를 초과하면 오히려 피부 트러블을 유발하는 문제가 있을 수 있다. 또한, 상기 컴프리잎 추출물이 30 중량부 미만이면 민간 피부 부위에 대한 진정 효과가 없을 수 있고, 70 중량부를 초과하면 비경제적이다. 또한, 상기 녹차 추출물이 15 중량부 미만이면 항산화 효과를 통한 피부 트러블 감소 효과가 없을 수 있고, 50 중량부를 초과하면 비경제적이다. 상기 식물 추출 혼합물의 각 추출물은 당업계에서 사용하는 일반적인 추출방법을 통해서 제조할 수 있으며, 바람직하게는 진공저온추출법, 초음파 추출법 등을 통해서 제조할 수 있다. 바람직한 일구현예를 들면, 상기 병풀 추출물은 건조된 병풀을 용매(부틸렌글리콜, 에탄올 및 증류수를 40 ~ 60 : 20 ~ 30 : 20 ~ 30 부피비로 혼합)에 1 : 1 ~ 30 중량비로 혼합한 후, 60 ~ 80℃에서 4 ~ 14 시간 동안, 바람직하게는 6 ~ 12 시간 동안 진공 저온 추출하여 병풀 추출물을 제조할 수 있다.The plant extract mixture includes Byeongchul extract, Cheongho extract, licorice extract, neem leaf extract, comfrey leaf extract and green tea extract, and preferably, based on 100 parts by weight of Byeongchul extract, 60-100 parts by weight of blueberry extract, 60-100 parts by weight of licorice extract Parts by weight, including 30 to 70 parts by weight of neem leaf extract, 30 to 70 parts by weight of comfrey leaf extract and 15 to 50 parts by weight of green tea extract, more preferably 70 to 90 parts by weight of Cheongho extract, It is good to include 60 to 85 parts by weight of licorice extract, 35 to 55 parts by weight of neem leaf extract, 35 to 60 parts by weight of comfrey leaf extract, and 25 to 40 parts by weight of green tea extract. At this time, if the amount of the cheongho extract is less than 60 parts by weight, there may be no skin regeneration effect on damaged skin, and if it exceeds 100 parts by weight, there may be a problem that increases the price and causes skin troubles. In addition, if the licorice extract is less than 60 parts by weight, there may be no soothing effect on angry skin, and if it exceeds 100 parts by weight, there may be a problem that only manufacturing cost increases due to excessive use. In addition, if the amount of the neem leaf extract is less than 30 parts by weight, there may be no effect of reducing itchiness and inflammation of the skin, and if it exceeds 70 parts by weight, there may be a problem that causes skin troubles. In addition, if the Comfrey leaf extract is less than 30 parts by weight, there may be no soothing effect on the private skin area, and if it exceeds 70 parts by weight, it is uneconomical. In addition, if the green tea extract is less than 15 parts by weight, there may not be an effect of reducing skin troubles through the antioxidant effect, and if it exceeds 50 parts by weight, it is uneconomical. Each extract of the plant extract mixture may be prepared through a general extraction method used in the art, and preferably may be prepared through a vacuum low temperature extraction method, an ultrasonic extraction method, or the like. For a preferred embodiment, the centella asiatica extract is a mixture of dried centella asiatica in a solvent (butylene glycol, ethanol, and distilled water mixed in a volume ratio of 40 to 60: 20 to 30: 20 to 30 by weight) at a weight ratio of 1: 1 to 30 Then, centella extract can be prepared by vacuum low temperature extraction at 60 to 80° C. for 4 to 14 hours, preferably for 6 to 12 hours.

그리고, 상기 청호 추출물, 감초 추출물, 님잎 추출물, 컴프리잎 추출물, 녹차 추출물 각각은 모두 앞서 설명한 병풀 추출물과 동일한 용매 및 방법으로 각각의 추출물을 제조할 수 있다.In addition, each of the Cheongho extract, licorice extract, neem leaf extract, comfrey leaf extract, and green tea extract may be prepared by using the same solvent and method as the centella asiatica extract described above.

발효에 사용되는 상기 발효 여과물은 비피다 발효 여과물, 락토바실러스 발효 여과물 및 효모 발효 여과물을 1 : 0.5 ~ 2 : 0.5 ~ 2 중량비로, 바람직하게는 1 : 0.8 ~ 1.5 : 0.8 ~ 1.5 중량비로, 더욱 바람직하게는 1 : 0.8 ~ 1.5 : 0.8 ~ 1.2 중량비로 포함하며, 이때, 각 발효 여과물이 상기 중량비를 벗어나면 식물 추출 혼합물의 발효가 잘 되지 않는 문제가 있을 수 있다.The fermentation filtrate used for fermentation is a Bifida fermentation filtrate, a Lactobacillus fermentation filtrate, and a yeast fermentation filtrate in a weight ratio of 1: 0.5 to 2: 0.5 to 2, preferably 1: 0.8 to 1.5: 0.8 to 1.5 In terms of weight ratio, more preferably 1: 0.8 to 1.5: 0.8 to 1.2 weight ratio. At this time, if each fermentation filtrate exceeds the weight ratio, there may be a problem in that fermentation of the plant extract mixture is not well done.

그리고, 상기 비피다 발효 여과물(Bifida Ferment Filtrate)은 ICID에 등재된 화장품 원료로서, 소화기계에 존재하는 혐기성 유산균인 비피도박테리아(Bifidobacteria)를 발효시켜 여과한 물질이다. 비피다 발효여과물은, 세포 재생 및 장벽 강화에 도움을 주는 성분으로서, 피부에서의 산소 공급을 활성화시킨다. 피부 장벽 강화로 거친 피부 개선 및 피부 리듬을 잡아주어 피부톤 개선과 수분 영양 공급 및 끈적임 없이 산듯한 발림성을 부여한다. 또한, 화장품의 원료로 사용되어 독성을 없애주는 역할을 하는 것으로 알려져 있다.In addition, the Bifida Ferment Filtrate is an ICID-registered cosmetic ingredient, and is a material obtained by fermenting Bifidobacteria, an anaerobic lactic acid bacteria present in the digestive system, and filtering. Bifida fermented filtrate is a component that helps regenerate cells and strengthens the barrier, and activates oxygen supply in the skin. By strengthening the skin barrier, it improves rough skin and holds the skin rhythm, improving skin tone, supplying moisture and nutrition, and providing smooth application without stickiness. It is also known to play a role in removing toxicity as it is used as a raw material for cosmetics.

또한, 상기 락토바실러스 발효 여과물은 상기 9종의 식물 추출물을 혼합하여 제조한 식물 추출 혼합물에 락토바실러스계 유산균을 접종한 후, 암실 및 혐기성 조건 하에서 20 ~ 40℃, 바람직하게는 30 ~ 35℃의 온도에서 24시간 이상, 바람직하게는 24 ~ 36 시간 발효시킨 후, 발효물을 70 ~ 90℃에서 5분 ~ 20분간 가열하여 유산균을 사멸시킨 후, 여과하여 수득한 여과물이다. 그리고, 바실러스계 유산균의 상기 접종은 식물 추출 혼합물 1mL 중에 1×105 ~ 1×108 CFU를, 바람직하게는 5×105 ~ 5×107 CFU를 접종하는 것이 좋다. 그리고, 상기 락토바실러스계 유산균으로는 락토바실러스 박테리아(Lactobacillus bacteria), 스트렙토코쿠스 써모필러스(Streptococcus thermophilus) 및 락토바실러스 락티스(Lactobacillus lactic) 중에서 선택된 1종 단독 또는 2종 이상을 혼합하여 사용할 수 있다.In addition, the Lactobacillus fermentation filtrate is inoculated with Lactobacillus-based lactic acid bacteria in a plant extract mixture prepared by mixing the 9 types of plant extracts, and then 20 to 40°C, preferably 30 to 35°C, under dark and anaerobic conditions. After fermentation at a temperature of 24 hours or more, preferably 24 to 36 hours, the fermented product is heated at 70 to 90° C. for 5 to 20 minutes to kill lactic acid bacteria, and then filtered. In addition, the inoculation of Bacillus-based lactic acid bacteria is preferably inoculated with 1×10 5 to 1×10 8 CFU, preferably 5×10 5 to 5×10 7 CFU in 1 mL of the plant extract mixture. In addition, as the Lactobacillus-based lactic acid bacteria, one selected from Lactobacillus bacteria, Streptococcus thermophilus, and Lactobacillus lactic may be used alone or in combination of two or more. have.

또한, 상기 효모 발효 여과물(Saccharomyces Ferment Filtrate)은 빵 또는 맥주를 만들 때 사용되는 천연 효모인 사카로미세스의 발효 여과물로서 아미노산, 핵산, 펩타이드, 미네랄, 비타민이 풍부하다. 효모 발효 여과물은 천연보습인자 NMF를 포함하고 아미노산 30%, 핵산 15%, 펩타이드 30% 이상을 포함하고 있으며, 상기 핵산은 피부 세포 대사의 필수적인 성분으로 피부 세포의 재활성화를 해주며 피부를 부드럽게 윤기 있게 하는 것으로 알려져 있다.In addition, the yeast fermentation filtrate (Saccharomyces Ferment Filtrate) is a fermentation filtrate of Saccharomyces, a natural yeast used when making bread or beer, and is rich in amino acids, nucleic acids, peptides, minerals, and vitamins. The yeast fermentation filtrate contains NMF, a natural moisturizing factor, and contains 30% amino acids, 15% nucleic acids, and 30% peptides, and the nucleic acids are essential components of skin cell metabolism, reactivating skin cells and softening the skin. It is known to make it shiny.

본 발명 제조에 사용되는 조성 중 식물 추출 복합 발효물은 식물 추출 혼합물에 상기 발효 여과물을 1 : 0.10 ~ 0.20 중량비로, 바람직하게는 1 : 0.12 ~ 0.18 중량비로 접종한 후, 30 ~ 37℃에서 36 ~ 58시간 동안, 바람직하게는 42 ~ 52시간 동안 발효시켜서 제조할 수 있다.Among the compositions used in the preparation of the present invention, the plant-extracted complex fermented product is inoculated with the fermented filtrate in a weight ratio of 1: 0.10 to 0.20, preferably in a weight ratio of 1: 0.12 to 0.18, and then inoculated at 30 to 37°C. It can be prepared by fermenting for 36 to 58 hours, preferably 42 to 52 hours.

1단계의 상기 혼합물 내 식물 추출 복합 발효물의 함량은 10 ~ 25 중량%를, 바람직하게는 12 ~ 22 중량%를, 더욱 바람직하게는 13 ~ 18 중량%로 사용할 수 있다. 이때, 식물 추출 복합 발효물의 함량이 10 중량% 미만이면 소취력 증대 효과가 없으며, 25 중량%를 초과하여 사용하더라도 더 이상의 소취력 증대 효과가 없으면서, 오히려 피부 자극을 유발할 수 있으므로 비경제적이다. The content of the plant-extracted complex fermented product in the mixture of step 1 may be used in an amount of 10 to 25% by weight, preferably 12 to 22% by weight, and more preferably 13 to 18% by weight. At this time, if the content of the plant-extracted complex fermentation product is less than 10% by weight, there is no effect of increasing deodorization, and even if it is used in excess of 25% by weight, there is no further effect of increasing deodorant power, and it is uneconomical because it may cause skin irritation.

1단계의 혼합물 중 상기 천연방부제는 소취제 내 유기계 성분의 변질, 부패를 방지하는 역할을 하는 것으로서, 당업계에서 사용하는 것을 사용할 수 있으나, 바람직하게는 카프릴릴글라이콜(Caprylyl glycol), 글리세릴카프릴레이트(Glyceryl Caprylate), 펜틸렌글라이콜(pentylene glycol), 1,2-헥산디올 및 더마소프트 1388(Dermasoft) 중에서 선택된 1종 이상을 사용할 수 있다. 그리고, 천연방부제의 사용량은 상기 혼합물 전체 중량 중 1.0 ~ 3.0 중량%를, 바람직하게는 1.6 ~ 2.4 중량%를, 더욱 바람직하게는 1.7 ~ 2.4 중량%를 사용할 수 있으며, 그 함량이 1.0 중량% 미만이면 식물 추출 복합 발효물 등이 변질되는 문제가 있을 수 있고, 그 함량이 3.0 중량% 초과하면 이로 인한 피부 트러블이 발생할 수 있고, 과량 사용이므로, 상기 범위 내로 사용하는 것이 좋다.In the mixture of step 1, the natural preservative plays a role of preventing deterioration and spoilage of organic components in the deodorant, and may be used in the art, but preferably caprylyl glycol, glyceryl car At least one selected from Glyceryl Caprylate, pentylene glycol, 1,2-hexanediol, and Dermasoft 1388 may be used. In addition, the amount of natural preservatives may be 1.0 to 3.0% by weight, preferably 1.6 to 2.4% by weight, more preferably 1.7 to 2.4% by weight of the total weight of the mixture, and the content is less than 1.0% by weight. In this case, there may be a problem of deterioration of the plant-extracted complex fermented product, etc., and if the content exceeds 3.0% by weight, skin problems may occur due to this, and since it is used in excess, it is recommended to use within the above range.

1단계의 상기 증점제는 소취 성분의 안정성 향상 역할을 하는 것으로서, 벤토나이트 등의 클레이류, 마그네슘 알루미늄 실리케이트 등의 무기계 증점제를 사용할 수 있으며, 바람직하게는 마그네슘 알루미늄 실리케이트(Magnesium Aluminum Silicate)를 사용할 수 있으며, 그 사용량은 상기 혼합물 전체 중량 중 0.1 ~ 3 중량%를, 바람직하게는 0.6 ~ 1.8 중량%를, 더욱 바람직하게는 0.8 ~ 1.5 중량%를 사용하는 것이 좋다. The thickener in the first step serves to improve the stability of the deodorant component, and an inorganic thickener such as clays such as bentonite and magnesium aluminum silicate may be used, and preferably, magnesium aluminum silicate may be used. The amount of the mixture is 0.1 to 3% by weight, preferably 0.6 to 1.8% by weight, and more preferably 0.8 to 1.5% by weight, based on the total weight of the mixture.

1단계의 상기 플로랄 워터(꽃수)는 혼합물 성분의 혼합을 위한 용매 역할, 향료 역할, 소취 향상 효과 증대 역할 및/또는 플로랄 워터 내 피부 개선 성분으로 인한 피부 트러블 방지 효과를 위해 사용하는 것으로서, 앞서 설명한 혼합물(또는 조성물) 성분 들 외에 혼합뭏 전체 중량 중 나머지 중량%를 차지한다. 상기 플로랄 워터는 병풀잎수, 라벤더꽃수, 포트마리골드꽃수, 로즈마리수 및 녹차수를 포함하며, 바람직하게는 병풀잎수 100 중량부에 대하여, 라벤더꽃수 0.05 ~ 5 중량부, 포트마리골드꽃수 0.05 ~ 5 중량부, 로즈마리수 0.05 ~ 3 중량부 및 녹차수 0.05 ~ 3 중량부를 포함하며, 더욱 바람직하게는 병풀잎수 100 중량부에 대하여, 라벤더꽃수 0.05 ~ 2 중량부, 포트마리골드꽃수 0.05 ~ 2 중량부, 로즈마리수 0.05 ~ 1 중량부 및 녹차수 0.05 ~ 1 중량부를 포함할 수 있다.The floral water (flower water) in step 1 is used as a solvent for mixing the components of the mixture, a fragrance, a role for enhancing deodorization, and/or for preventing skin troubles caused by skin improvement ingredients in the floral water. In addition to the components of the mixture (or composition), the mixture accounts for the remaining weight% of the total weight. The floral water includes centella leaf water, lavender flower water, port marigold flower water, rosemary water, and green tea water, and preferably, based on 100 parts by weight of centella leaf water, the number of lavender flowers is 0.05 to 5 parts by weight, and the number of port marigold flowers is 0.05. ~ 5 parts by weight, 0.05 to 3 parts by weight of rosemary water, and 0.05 to 3 parts by weight of green tea water, more preferably 0.05 to 2 parts by weight of lavender flowers, 0.05 to 2 parts by weight of pot marigold flowers based on 100 parts by weight of centella leaves. It may contain 2 parts by weight, 0.05 to 1 part by weight of rosemary water, and 0.05 to 1 part by weight of green tea water.

상기 플로랄 워터는 저온 임계 추출법으로 추출한 것으로서, 바람직한 일례를 들면, 건조된 병풀잎, 라벤더꽃, 포트마리골드꽃, 로즈마리 잎 및/또는 로즈마리 잎 줄기, 녹차잎 각각 또는 이들을 혼합한 혼합물을 초고속 진공저온 추출기에 증류수와 1 : 1 ~ 30 중량비로, 바람직하게는 1: 3 ~ 25 중량비로 혼합한 후, 약 60 ~ 80℃에서 8 ~ 12시간 동안 추출하는 1단계; 1단계의 추출물을 진공 저온추출기에 넣고, 농축 및 방냉하는 2단계;를 포함하는 공정을 수행하여 제조한 것일 수 있다. 그리고, 상기 플로랄 워터는 사용시에 희석하여 사용할 수도 있다.The floral water is extracted by a low-temperature critical extraction method, and a preferred example is, for example, dried centella leaves, lavender flowers, pot marigold flowers, rosemary leaves and/or rosemary leaf stems, green tea leaves, or a mixture of them at ultra high speed vacuum low temperature. 1 step of mixing distilled water and 1: 1 to 30 weight ratio, preferably 1: 3 to 25 weight ratio in the extractor, and then extracting for 8 to 12 hours at about 60 to 80 ℃; It may be prepared by performing a process including; step 1 of putting the extract of step 1 into a vacuum low-temperature extractor, and concentrating and cooling it. In addition, the floral water may be diluted when used.

다음으로 본 발명의 위생재용 소취제 제조방법의 2단계는 1단계의 혼합물을 미분쇄 공정을 수행하여 미분쇄물을 수득하는 공정이다. Next, step 2 of the method for producing a deodorant for hygiene according to the present invention is a step of obtaining a finely pulverized product by performing a fine pulverization process of the mixture of step 1.

상기 미분쇄 공정을 당업계에서 사용하는 일반적인 미분쇄 방법을 통해 수행할 수 있으며, 바람직하게는 유성 압연기(Planetary mill)를, 더욱 바람직하게는 유성 바스켓 압연기(Planetary basket mill)를 사용하여 수행할 수 있다. 미분쇄 방법의 바람직한 일구현예를 들면, 유성 바스켓 압연기에 1단계의 혼합물을 투입한 후, 비드 직경 1.0 ~ 2.5 mm, 아웃터 모터(outer motor) 500 ~ 800 rpm 및 이너 모터(inner motor) 800 ~ 1000 rpm 조건 하에서 미분쇄를 수행하여 미분쇄물을 수득할 수 있다.The pulverization process can be carried out through a general pulverization method used in the art, preferably a planetary mill, more preferably a planetary basket mill. have. For example, a preferred embodiment of the pulverization method is, after injecting the mixture of step 1 into a planetary basket rolling machine, a bead diameter of 1.0 ~ 2.5 mm, an outer motor 500 ~ 800 rpm, and an inner motor 800 ~ Fine pulverization can be performed under conditions of 1000 rpm to obtain a fine pulverized product.

다음으로, 상기 3단계는 미분쇄물을 건조시켜서 최종 파우더, 즉 분말 형태의 본 발명의 소취제를 수득하는 공정이다. 이때, 상기 건조 방법은 특별하게 한정하지 않으며, 일반적인 건조 방법을 통해서 수행할 수 있으며, 바람직한 일례를 들면, 2단계의 미분쇄물을 오븐에 투입한 후, 50 ~ 80℃ 에서 5분 ~ 30분 동안 건조를 수행할 수 있다. Next, the third step is a process of drying the finely pulverized material to obtain a final powder, that is, the deodorant of the present invention in powder form. At this time, the drying method is not particularly limited, and can be carried out through a general drying method. For example, after putting the finely pulverized material of step 2 into an oven, it is 5 to 30 minutes at 50 to 80°C. While drying can be carried out.

3단계의 건조를 수행하면 2단계의 미분쇄물 내 있던 식물 추출 복합 발효물 내 수분 및 플로랄 워터 내 수분 증발하면서 소취 성분 및/또는 피부 개선 물질 등의 기능성 성분이 소취제에 남게 된다. When the drying in the third step is performed, the moisture in the plant-extracted complex fermentation product in the second step of the fine pulverized product and the moisture in the floral water evaporate, leaving functional ingredients such as deodorant ingredients and/or skin improvement substances in the deodorant.

이렇게 3단계 공정을 수행하여 제조한 본 발명의 위생재용 소취제는 분말(파우더) 타입으로서, 평균입도 0.2㎛ ~ 5.0㎛, 바람직하게는 0.2㎛ ~ 4.0㎛, 더욱 바람직하게는 0.5㎛ ~ 3.5㎛ 일 수 있다.The deodorant for sanitary products of the present invention prepared by performing the three-step process is a powder (powder) type, and has an average particle size of 0.2 µm to 5.0 µm, preferably 0.2 µm to 4.0 µm, more preferably 0.5 µm to 3.5 µm. I can.

이러한, 본 발명의 소취제를 이용하여 소취 기능을 가지는 섬유, 부직포, 시트 등의 섬유 제품을 제조할 수 있으며, 또한 기저귀 및 여성용 생리대 등의 위생재에 적용하기에 적합하다.Using the deodorant of the present invention, fibrous products such as fibers, nonwoven fabrics, and sheets having a deodorizing function can be produced, and are suitable for use in sanitary materials such as diapers and sanitary napkins for women.

이하, 실시예를 통하여 본 발명을 더욱 구체적으로 설명하기로 하지만, 하기 실시예가 본 발명의 범위를 제한하는 것은 아니며, 이는 본 발명의 이해를 돕기 위한 것으로 해석되어야 할 것이다.Hereinafter, the present invention will be described in more detail through examples, but the following examples do not limit the scope of the present invention, which should be interpreted to aid understanding of the present invention.

[[ 실시예Example ] ]

준비예Preparation example 1 : One : 플로랄Floral 워터(꽃수)의Of water 제조 Produce

(1) (One) 병풀잎수의Centella asiatica 제조 Produce

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조 병풀잎(Centella Asiatica Leaf)을 증류수에 1:3 중량비로 넣고, 약 80℃에서 10 시간 동안 추출하여 병풀잎 플로랄 워터를 얻었다. 이 플로랄 워터를 다시 상기 진공 저온추출기에 넣고, 농축 및 방냉하여 냉장(약 3℃) 보관하였다.Centella Asiatica Leaf (Centella Asiatica Leaf) was added to distilled water at a weight ratio of 1:3 in an ultra-high-speed vacuum low-temperature extractor (Gyeongseo Machinery, COSMOS-660), and extracted at about 80° C. for 10 hours to obtain a Centella Asiatica Leaf floral water. This floral water was again put into the vacuum low-temperature extractor, concentrated, cooled, and stored in a refrigerator (about 3° C.).

(2) (2) 라벤더수의Lavender 제조 Produce

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조된 라벤더(Lavandula Angustifolia) 꽃과 잎과 증류수를 1:1 중량비로 넣고, 약 75∼77℃에서 10 시간 동안 추출하여 라벤더 플로랄 워터를 얻었다. 이 플로랄 워터를 다시 상기 진공 저온추출기에 넣고, 농축하여 라벤더 식물 추출 성분이 30∼50중량%가 되도록 하였다. 이를 방냉하여 냉장(약 3℃) 보관하였다.Lavender (Lavandula Angustifolia) flowers, leaves, and distilled water dried in an ultra-high-speed vacuum low-temperature extractor (Gyeongseo Machinery, COSMOS-660) were added in a 1:1 weight ratio, and extracted at about 75-77°C for 10 hours to obtain lavender floral water. This floral water was again put into the vacuum low-temperature extractor, and concentrated so that the lavender plant extract component was 30-50% by weight. This was allowed to cool and stored refrigerated (about 3°C).

(3) (3) 포트마리골드꽃수의Port marigold flower 제조 Produce

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조된 포트마리골드(Calendula officinalis) 꽃을 증류수에 1:20 중량비로 넣고, 약 75℃에서 5 시간 동안 추출하여 포트마리골드 플로랄 워터를 얻었다. 이 플로랄 워터를 다시 상기 진공 저온추출기에 넣고, 농축 및 방냉하여 냉장(약 3℃) 보관하였다.Pot Marigold (Calendula officinalis) flowers dried in an ultra-high-speed vacuum low-temperature extractor (Kyungseo Machinery, COSMOS-660) were added to distilled water at a weight ratio of 1:20, and extracted at about 75°C for 5 hours to obtain portmarigold floral water. This floral water was again put into the vacuum low-temperature extractor, concentrated, cooled, and stored in a refrigerator (about 3° C.).

(4) (4) 로즈마리수의Rosemary 제조 Produce

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조된 로즈마리(Rosmarinus Officinalis )의 잎 및 줄기를 증류수에 약 1:20 중량비로 넣고, 약 75℃에서 5 시간 동안 추출하여 로즈마리 플로랄 워터를 얻었다. 이 플로랄 워터를 다시 상기 진공 저온추출기에 넣고, 농축 및 방냉하여 냉장(약 3℃) 보관하였다.The leaves and stems of rosemary (Rosmarinus Officinalis) dried in an ultra-high-speed vacuum low-temperature extractor (Gyeongseo Machinery, COSMOS-660) were added to distilled water at a weight ratio of about 1:20, and extracted at about 75° C. for 5 hours to obtain rosemary floral water. This floral water was again put into the vacuum low-temperature extractor, concentrated, cooled, and stored in a refrigerator (about 3° C.).

(5) (5) 녹차수의Green tea 제조 Produce

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조된 녹차잎(Camellia Sinensis Leaf)을 증류수에 1:20 중량비로 넣고, 약 75℃에서 5 시간 동안 추출하여 로즈마리 플로랄 워터를 얻었다. 이 플로랄 워터를 다시 상기 진공 저온추출기에 넣고, 농축 및 방냉하여 냉장(약 3℃) 보관하였다.Green tea leaves (Camellia Sinensis Leaf) dried in an ultra-high-speed vacuum low-temperature extractor (Gyeongseo Machinery, COSMOS-660) were added to distilled water at a weight ratio of 1:20, and extracted at about 75° C. for 5 hours to obtain rosemary floral water. This floral water was again put into the vacuum low-temperature extractor, concentrated, cooled, and stored in a refrigerator (about 3° C.).

(6) 혼합 (6) mixed 플로랄Floral 워터Water (( 꽃수Number of flowers ) 제조) Produce

상기 병풀잎수 100 중량부에 대하여, 라벤더꽃수 0.15 중량부, 포트마리골드꽃수 0.15 중량부, 로즈마리수 0.15 중량부 및 녹차수 0.15 중량부를 혼합하여 플로랄 워터를 제조하였다.Floral water was prepared by mixing 0.15 parts by weight of lavender flower water, 0.15 parts by weight of pot marigold flower water, 0.15 parts by weight of rosemary water, and 0.15 parts by weight of green tea water with respect to 100 parts by weight of centella leaf water.

준비예Preparation example 2 : 식물 추출 복합 2: plant extract complex 발효물의Fermented 제조 Produce

(1) 식물 추출 혼합물의 제조(1) Preparation of plant extract mixture

초고속 진공저온추출기(경서기계, COSMOS-660)에 건조 병풀을 부틸렌글리콜/에탄올/증류수(50/25/25 부피비)의 용매에1:5 중량비로 넣고, 약 75℃에서 12시간 동안 추출하여 병풀 추출물을 얻었다. 얻어진 추출물을 증류하여 유기용매를 회수하였다. 추출물의 농도는 약 5% 정도이었다. 이를 다시 농축하여 추출물 중의 수분을 50% 정도 제거하였다. 이렇게 얻어진 병풀 추출물을 냉장(약 3℃) 보관하였다.Put dry centella in an ultra-high-speed vacuum low-temperature extractor (Kyungseo Machinery, COSMOS-660) in a solvent of butylene glycol/ethanol/distilled water (50/25/25 volume ratio) at a weight ratio of 1:5, and extract at about 75℃ for 12 hours. Centella asiatica extract was obtained. The obtained extract was distilled to recover an organic solvent. The concentration of the extract was about 5%. It was concentrated again to remove about 50% of moisture in the extract. The centella asiatica extract thus obtained was stored refrigerated (about 3°C).

청호, 감초, 님잎, 컴프리잎, 녹차 각각을 상기 병출 추출물과 동일하게 조제하여 청호 추출물, 감초 추출물, 님잎 추출물, 컴프리잎 추출물, 녹차 추출물 각각을 제조하였다.Cheongho, licorice, neem leaf, comfrey leaf, and green tea were each prepared in the same manner as the Byeongchul extract to prepare each of the cheongho extract, licorice extract, neem leaf extract, comfrey leaf extract, and green tea extract.

다음으로, 상기 병풀 추출물 100 중량부에 대하여, 청호 추출물 75 중량부, 감초 추출물 75 중량부, 님잎 추출물 45 중량부, 컴프리잎 추출물 45 중량부, 녹차 추출물 31.5 중량부를 혼합하여 식물 추출 혼합물을 제조하였다.Next, with respect to 100 parts by weight of centella asiatica extract, 75 parts by weight of Cheongho extract, 75 parts by weight of licorice extract, 45 parts by weight of neem leaf extract, 45 parts by weight of comfrey leaf extract, and 31.5 parts by weight of green tea extract were mixed to prepare a plant extract mixture. .

(2) 발효 (2) fermentation 여과물의Filtrate 준비 Preparations

비피다 발효 여과물, 락토바실러스 발효 여과물 및 효모 발효 여과물을 1 : 1: 1 중량비로 준비하였다.Bifida fermentation filtrate, Lactobacillus fermentation filtrate, and yeast fermentation filtrate were prepared in a 1: 1: 1 weight ratio.

이때, 상기 비피다 발효 여과물 및 효모 발효 여과물(사카로미세스 효모 발효 여과물)은 시중에 판매되는 것을 구입하여 사용하였다.At this time, the Bifida fermentation filtrate and yeast fermentation filtrate (Saccharomyces yeast fermentation filtrate) were purchased and used.

그리고, 상기 락토바실러스 발효 여과물은 상기 식물 추출 혼합물 1mL 중 락토바실러스계 유산균인 락토바실러스 박테리아(Lactobacillus bacteria)을 1.2×106 ~ 1.5×106 CFU 을 접종한 후, 암실 및 혐기성 조건 하에서 약 30 ~ 32℃의 온도에서 26 시간 동안 발효시킨 후, 발효물을 85℃에서 15분간 가열하여 유산균을 사멸시킨 후, 여과하여 수득한 여과물이다. In addition, the Lactobacillus fermentation filtrate was inoculated with 1.2×10 6 ~ 1.5×10 6 CFU of Lactobacillus bacteria, which is a Lactobacillus-based lactic acid bacterium in 1 mL of the plant extract mixture, and then about 30 under dark and anaerobic conditions. After fermentation at a temperature of ~ 32°C for 26 hours, the fermented product was heated at 85°C for 15 minutes to kill lactic acid bacteria, and then filtered.

(3) 식물 추출 복합 (3) plant extract complex 발효물의Fermented 제조 Produce

상기 식물 추출 혼합물 100 중량부에 상기 발효 여과물 16.1 중량부를 접종한 후, 35 ~ 38℃에서 48 시간 동안 발효시켜서 식물 추출 복합 발효물을 제조하였다.After inoculating 16.1 parts by weight of the fermentation filtrate to 100 parts by weight of the plant extract mixture, fermentation was performed at 35 to 38° C. for 48 hours to prepare a plant extract complex fermentation product.

실시예Example 1 : One : 소취제의Deodorant 제조 Produce

실리카(Cas No. 7631-86-9) 65 중량%, 이산화아연(Cas No. 1314-13-2) 25 중량% 및 이산화티탄 15 중량%를 혼합하여 세라믹 콜로이드를 준비하였다. 이때, 세라믹 콜로이드의 평균입도는 약 0.2 ~ 1.2㎛였다(도 1의 광학현미경 사진 참조).A ceramic colloid was prepared by mixing 65% by weight of silica (Cas No. 7631-86-9), 25% by weight of zinc dioxide (Cas No. 1314-13-2), and 15% by weight of titanium dioxide. At this time, the average particle size of the ceramic colloid was about 0.2 ~ 1.2㎛ (refer to the optical microscope picture in FIG. 1).

상기 세라믹 콜로이드, 준비예 2에서 제조한 식물 추출 복합 발효물, 천연방부제인 펜틸렌글라이콜(CAS no: 5343-92-0), 증점제인 비검 HV(VEEGUM® HV) 및 상기 준비예 1에서 제조한 플로랄 워터를 하기 표 1과 같이 혼합하여 혼합물을 제조하였다.The ceramic colloid, plant-extracted complex fermented product prepared in Preparation Example 2, pentylene glycol (CAS no: 5343-92-0) as a natural preservative, Veegum HV (VEEGUM ® HV) as a thickener, and prepared in Preparation Example 1 A mixture was prepared by mixing one floral water as shown in Table 1 below.

다음으로, 상기 혼합물을 유성 바스켓 압연기(Planetary basket mill)에 투입 후, 습식 밀(직경 1.0mm의 볼 및 직경 2.5 mm의 볼= 1:1 중량비)을 이용하여아웃터모터(outer motor) 약 650 rpm 및 이너모터(inner motor) 900 rpm 조건 하에서 미분쇄를 수행하여 미분쇄물을 수득하였다.Next, after introducing the mixture into a planetary basket mill, an outer motor of about 650 rpm using a wet mill (a ball having a diameter of 1.0 mm and a ball having a diameter of 2.5 mm = 1:1 weight ratio). And fine pulverization under 900 rpm conditions of an inner motor to obtain a fine pulverized product.

다음으로, 상기 미분쇄물을 오븐에 투입한 후, 70 ~ 72℃ 에서 약 20분 동안 건조를 수행한 후, 서냉시켜서 분말(또는 파우더)인 평균입도 약 2.5㎛의 소취제를 수득하였다. 제조한 소취제는 냉장실(약 3℃)에 보관하였다.Next, the finely pulverized material was put in an oven, dried at 70 to 72° C. for about 20 minutes, and then slowly cooled to obtain a deodorant having an average particle size of about 2.5 μm as a powder (or powder). The prepared deodorant was stored in a refrigerator (about 3°C).

실시예Example 2 ~ 4 및 2 to 4 and 비교예Comparative example 1 ~ 4 1 to 4

상기 실시예 1과 동일한 조성을 사용하되, 하기 표 1과 같은 조성비로 소취제를 제조하여 실시예 2 ~ 4 및 비교예 1 ~ 4 를 각각 실시하였다.The same composition as in Example 1 was used, but a deodorant was prepared in the composition ratio shown in Table 1 below, and Examples 2 to 4 and Comparative Examples 1 to 4 were each performed.

비교예 1의 경우, 실시예 1과 동일한 조성 미 조성비를 사용하여 제조하되, 세라믹 콜로이드를 평균입도 3.0 ~ 3.5㎛인 것을 사용하였다.In the case of Comparative Example 1, but prepared using the same composition non-composition ratio as in Example 1, a ceramic colloid having an average particle size of 3.0 ~ 3.5㎛ was used.

구분
(중량%)
division
(weight%)
세라믹
콜로이드
ceramic
Colloid
식물추출
복합
발효물
Plant extract
complex
Fermentation
천연방부제Natural preservatives 증점제Thickener 플로랄
워터
Floral
Water
실시예 1Example 1 62 중량%62% by weight 16 중량%16% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 실시예 2Example 2 56 중량%56% by weight 16 중량%16% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 실시예 3Example 3 62 중량%62% by weight 12 중량%12% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 실시예 4Example 4 62 중량%62% by weight 22 중량%22% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 비교예 1Comparative Example 1 62 중량%62% by weight 16 중량%16% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 비교예 2Comparative Example 2 67 중량%67% by weight 16 중량%16% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 비교예 3Comparative Example 3 62 중량%62% by weight 9 중량%9% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance 비교예 4Comparative Example 4 62 중량%62% by weight 26 중량%26% by weight 2.2중량%2.2% by weight 1.2중량%1.2% by weight 나머지 잔량Remaining balance

제조예Manufacturing example 1 : One : 위생재용For hygiene SAP(Super Absorbent Polymer) 시트의 제조 Manufacturing of SAP (Super Absorbent Polymer) sheet

140 gsm(gram per square Meter) SAP 파우더(시미토모사 제품)를 준비하였다.140 gsm (gram per square meter) SAP powder (manufactured by Shimitomo Corporation) was prepared.

상기 SAP 파우더와 실시예 1에서 제조한 소취제, 펄프 및 티슈를 골고루 혼합한 후, 평평하게 형성될 수 있도록 압착하고, 핫멜트로 고정시켰다(표 2 참조). The SAP powder and the deodorant prepared in Example 1, pulp, and tissue were evenly mixed, pressed to form a flat, and fixed with a hot melt (see Table 2).

구분division 함량(중량%)Content (% by weight) SAP 파우더SAP powder 50 중량%50% by weight 소취제Deodorant 8 중량%8% by weight 펄프(pulp)Pulp 30 중량%30% by weight 티슈(tissue)Tissue 15 중량%15% by weight

제조예Manufacturing example 2 ~ 4 및 2 to 4 and 비교제조예Comparative Production Example 1 ~ 4 1 to 4

상기 제조예 1과 동일한 방법으로 위생재용 SAP 시트를 제조하되, 실시예 1 대신 실시예 2 ~ 4 또는 비교제조예 1 ~ 4의 소취제 각각을 이용하여 위생재용 SAP 시트를 각각 제조하여, 제조예 2 ~ 4 및 비교제조예 1 ~ 4를 실시하였다.In the same manner as in Preparation Example 1, an SAP sheet for sanitary materials was prepared, but instead of Example 1, SAP sheets for sanitary materials were each prepared using the deodorants of Examples 2 to 4 or Comparative Preparation Examples 1 to 4, respectively, ~ 4 and Comparative Preparation Examples 1 to 4 were carried out.

실험예Experimental example 1 : 암모니아에 대한 1: against ammonia 소취력Deodorant 측정 Measure

실시예 1 ~ 4 및 비교예 1 ~ 4의 소취제를 이용하여, 제조예 1 ~ 4 및 비교제조예 1 ~ 4에서 제조한 위생재용 SAP(Super Absorbent Polymer) 시트에 대한 암모니아에 대한 소취력을 FITI 시험연구원에 의뢰하여 가스검지관법에 의해 측정하였고, 그 결과를 하기 표 4에 나타내었다. 그리고, 시험방법은 표 3와 같다.Using the deodorant of Examples 1 to 4 and Comparative Examples 1 to 4, FITI deodorizing power against ammonia for the SAP (Super Absorbent Polymer) sheet for sanitary materials prepared in Preparation Examples 1 to 4 and Comparative Preparation Examples 1 to 4 It was requested to a test research institute and measured by the gas detection tube method, and the results are shown in Table 4 below. And, the test method is shown in Table 3.

그리고, 측정에 사용된 실시예 1의 소취제 사진은 도 2에 나타내었고, 제조예 1의 위생제용 SAP 시트 사진을 도 3에 나타내었다.And, a photograph of the deodorant of Example 1 used for the measurement is shown in FIG. 2, and a photograph of the SAP sheet for sanitary agent of Preparation Example 1 is shown in FIG. 3.

* 소취제 시편: 1g / SAP 시트 시편 : 가로×세로, 7cm × 20cm
* 가스백 : 5 L 테트라백
* 가스백 내 가스량 : 3L
* 측정시간 : 2 기간 경과 후
* 초기농도 : 암모니아 100 ppm
* 탈취율(%) = ((Cb-Cs)/Cb)×100
Cb : Blank, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
Cs : 시료, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
* Deodorant specimen: 1g / SAP sheet specimen: horizontal × length, 7cm × 20cm
* Gas bag: 5 L tetrabag
* Gas volume in gas bag: 3L
* Measurement time: after 2 periods
* Initial concentration: 100 ppm of ammonia
* Deodorization rate (%) = ((Cb-Cs)/Cb)×100
Cb: Blank, concentration of test gas remaining in the test gas bag after 2 hours
Cs: Sample, concentration of test gas remaining in the test gas bag after 2 hours

구분division 암모니아 탈취율(%)Ammonia deodorization rate (%) 위생재용
SAP 시트
For hygiene
SAP sheet
제조예 1Manufacturing Example 1 > 99.8> 99.8
제조예 2Manufacturing Example 2 97.897.8 제조예 3Manufacturing Example 3 99.099.0 제조예 4Manufacturing Example 4 99.999.9 비교제조예 1Comparative Production Example 1 98.598.5 비교제조예 2Comparative Production Example 2 99.699.6 비교제조예 3Comparative Production Example 3 96.496.4 비교제조예 4Comparative Production Example 4 > 99.8> 99.8

실험예Experimental example 2 : 트리메틸아민에 대한 2: for trimethylamine 소취력Deodorant 측정 Measure

실시예 1 ~ 4 및 비교예 1 ~ 4의 소취제를 이용하여, 제조예 1 ~ 4 및 비교제조예 1 ~ 4에서 제조한 위생재용 SAP(Super Absorbent Polymer) 시트에 대한 트리메틸아민에 대한 소취력을 FITI 시험연구원에 의뢰하여 가스검지관법에 의해 측정하였고, 그 결과를 하기 표 6에 나타내었다. 그리고, 시험방법은 표 5와 같다.Using the deodorant of Examples 1 to 4 and Comparative Examples 1 to 4, the deodorizing power for trimethylamine for the SAP (Super Absorbent Polymer) sheet for sanitary materials prepared in Preparation Examples 1 to 4 and Comparative Preparation Examples 1 to 4 The measurement was performed by the gas detection tube method by requesting the FITI test research institute, and the results are shown in Table 6 below. And, the test method is shown in Table 5.

* 소취제 시편: 1g / SAP 시트 시편 : 가로×세로, 10cm × 10cm
* 가스백 : 5 L 테트라백
* 가스백 내 가스량 : 3L
* 측정시간 : 2 기간 경과 후
* 초기농도 : 트리메틸아민 28 ppm
* 탈취율(%) = ((Cb-Cs)/Cb)×100
Cb : Blank, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
Cs : 시료, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
* Deodorant specimen: 1g / SAP sheet specimen: width × length, 10cm × 10cm
* Gas bag: 5 L tetrabag
* Gas volume in gas bag: 3L
* Measurement time: after 2 periods
* Initial concentration: Trimethylamine 28 ppm
* Deodorization rate (%) = ((Cb-Cs)/Cb)×100
Cb: Blank, concentration of test gas remaining in the test gas bag after 2 hours
Cs: Sample, concentration of test gas remaining in the test gas bag after 2 hours

구분division 트리메틸아민 탈취율(%)Trimethylamine deodorization rate (%) 위생재용
SAP 시트
For hygiene
SAP sheet
제조예 1Manufacturing Example 1 > 99.6> 99.6
제조예 2Manufacturing Example 2 98.198.1 제조예 3Manufacturing Example 3 96.996.9 제조예 4Manufacturing Example 4 > 99.6> 99.6 비교제조예 1Comparative Production Example 1 99.099.0 비교제조예 2Comparative Production Example 2 99.299.2 비교제조예 3Comparative Production Example 3 95.195.1 비교제조예 4Comparative Production Example 4 > 99.7> 99.7

실험예Experimental example 3 : 황화수소에 대한 3: for hydrogen sulfide 소취력Deodorant 측정 Measure

실시예 1 ~ 4 및 비교예 1 ~ 4 의 소취제를 이용하여, 제조예 1 ~ 4 및 비교제조예 1 ~ 4에서 제조한 위생재용 SAP(Super Absorbent Polymer) 시트에 대한 트리메틸아민에 대한 소취력을 KOTITI 시험연구원에 의뢰하여 측정하였고, 그 결과를 하기 표 8에 나타내었다. 그리고, 시험방법은 표 7과 같다.Using the deodorant of Examples 1 to 4 and Comparative Examples 1 to 4, the deodorizing power of trimethylamine for the SAP (Super Absorbent Polymer) sheet for sanitary materials prepared in Preparation Examples 1 to 4 and Comparative Preparation Examples 1 to 4 Measurement was conducted by requesting the KOTITI Test Research Institute, and the results are shown in Table 8 below. And, the test method is shown in Table 7.

* 소취제 시편: 1g / SAP 시트 시편 : 가로×세로, 10cm × 10cm
* 가스백 : 5 L 테트라백
* 가스백 내 가스량 : 3L
* 측정시간 : 2 기간 경과 후
* 초기농도 : 황화수소 4.0 mg/kg
* 탈취율(%) = ((Cb-Cs)/Cb)×100
Cb : Blank, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
Cs : 시료, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
* Deodorant specimen: 1g / SAP sheet specimen: width × length, 10cm × 10cm
* Gas bag: 5 L tetrabag
* Gas volume in gas bag: 3L
* Measurement time: after 2 periods
* Initial concentration: Hydrogen sulfide 4.0 mg/kg
* Deodorization rate (%) = ((Cb-Cs)/Cb)×100
Cb: Blank, concentration of test gas remaining in the test gas bag after 2 hours
Cs: Sample, concentration of test gas remaining in the test gas bag after 2 hours

구분division 황화수소 탈취율(%)Hydrogen sulfide deodorization rate (%) 위생재용
SAP 시트
For hygiene
SAP sheet
제조예 1Manufacturing Example 1 > 99.9> 99.9
제조예 2Manufacturing Example 2 98.998.9 제조예 3Manufacturing Example 3 99.299.2 제조예 4Manufacturing Example 4 > 99.9> 99.9 비교제조예 1Comparative Production Example 1 99.499.4 비교제조예 2Comparative Production Example 2 99.799.7 비교제조예 3Comparative Production Example 3 98.098.0 비교제조예 4Comparative Production Example 4 > 99.9> 99.9

실험예Experimental example 4 : 4 : 메틸멀캅탄에To methyl mercaptan 대한 About 소취력Deodorant 측정 Measure

실시예 1 ~ 4 및 비교예 1 ~ 4 의 소취제를 이용하여 제조예 1 ~ 4 및 비교제조예 1 ~ 4에서 제조한 위생재용 SAP(Super Absorbent Polymer) 시트에 대한 메틸머캅탄에 대한 소취력을 KOTITI 시험연구원에 의뢰하여 측정하였고, 그 결과를 하기 표 10에 나타내었다. 그리고, 시험방법은 표 9와 같다.Using the deodorant of Examples 1 to 4 and Comparative Examples 1 to 4, the deodorizing power of methyl mercaptan for the SAP (Super Absorbent Polymer) sheet for sanitary materials prepared in Preparation Examples 1 to 4 and Comparative Preparation Examples 1 to 4 Measurement was conducted by requesting KOTITI Test Research Institute, and the results are shown in Table 10 below. And, the test method is shown in Table 9.

* 소취제 시편: 1g / SAP 시트 시편 : 가로×세로, 10cm×10cm
* 가스백 : 5 L 테트라백
* 가스백 내 가스량 : 3L
* 측정시간 : 2 기간 경과 후
* 초기농도 : 메틸멀캅탄 8 ppm
* 탈취율(%) = ((Cb-Cs)/Cb)×100
Cb : Blank, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
Cs : 시료, 2시간 경과 후, 시험가스백 안에 남아 있는 시험가스의 농도
* Deodorant specimen: 1g / SAP sheet specimen: width × length, 10cm × 10cm
* Gas bag: 5 L tetrabag
* Gas volume in gas bag: 3L
* Measurement time: after 2 periods
* Initial concentration: 8 ppm methyl mercaptan
* Deodorization rate (%) = ((Cb-Cs)/Cb)×100
Cb: Blank, concentration of test gas remaining in the test gas bag after 2 hours
Cs: Sample, concentration of test gas remaining in the test gas bag after 2 hours

구분division 메틸멀캅탄 탈취율(%)Methyl mercaptan deodorization rate (%) 위생재용
SAP 시트
For hygiene
SAP sheet
제조예 1Manufacturing Example 1 > 99.3> 99.3
제조예 2Manufacturing Example 2 98.898.8 제조예 3Manufacturing Example 3 98.298.2 제조예 4Manufacturing Example 4 99.799.7 비교제조예 1Comparative Production Example 1 99.099.0 비교제조예 2Comparative Production Example 2 99.199.1 비교제조예 3Comparative Production Example 3 94.994.9 비교제조예 4Comparative Production Example 4 99.799.7

상기 표 4(암모니아 탈취율), 표 6(트리메틸아민 탈취율), 표8(황화수소 탈취율), 표 10(메틸멀캅탄 탈취율) 측정 결과를 살펴보면, 본 발명의 소취제(실시예 1 ~ 4)를 사용하여 제조한 위생재용 SAP 시트는 전반적으로 매우 높은 탈취율을 보임을 확인할 수 있다. 그리고, 세라믹 콜로이드 평균입경이 2㎛를 초과한 것을 사용한 비교제조예 1및 세라믹 콜로이드를 과량 함유한 비교제조예 2의 경우, 제조예 1과 비교할 때, 전반적으로 낮은 소취력을 보이는 경향이 있었다. 또한, 소취제 내 식물추출복합 발효물 함량이 10 중량% 미만으로 사용한 비교예 3을 사용하여 제조한 SAP 시트(비교제조예 3)의 경우, 제조예 3과 비교할 때, 전반적인 탈취 효과가 급감하는 경향이 있었다. 그리고, 소취제 내 식물추출복합 발효물 함량이 25 중량% 초과 사용한 비교예 4를 사용하여 제조한 SAP 시트(비교제조예 4)의 제조예 4와 비교할 때, 과량 사용으로 인한 소취 효과 증대가 없었다.Looking at the measurement results in Table 4 (ammonia deodorization rate), Table 6 (trimethylamine deodorization rate), Table 8 (hydrogen sulfide deodorization rate), and Table 10 (methyl mercaptan deodorization rate), the deodorant of the present invention (Examples 1 to 4) was used. It can be seen that the manufactured SAP sheet for sanitary materials shows a very high deodorization rate overall. In addition, in the case of Comparative Production Example 1 using a ceramic colloid having an average particle diameter exceeding 2 μm and Comparative Production Example 2 containing an excessive amount of ceramic colloid, as compared with Preparation Example 1, there was a tendency to show a low overall deodorizing power. In addition, in the case of the SAP sheet (Comparative Preparation Example 3) prepared using Comparative Example 3 in which the content of the plant extract complex fermentation product in the deodorant was less than 10% by weight, compared to Preparation Example 3, the overall deodorizing effect tended to decrease sharply. There was this. And, compared with Preparation Example 4 of the SAP sheet (Comparative Preparation Example 4) prepared using Comparative Example 4 in which the content of the plant extract complex fermentation product was used in excess of 25% by weight in the deodorant, there was no increase in the deodorizing effect due to excessive use.

상기 실시예 및 실험예를 통해서 본 발명의 소취제 및 이를 이용한 위생재용 SAP 시트가 암모니아, 황화수소, 트리메틸아민 및 메틸머캅탄에 대한 우수한 소취력을 갖는 것을 확인할 수 있었다.Through the above Examples and Experimental Examples, it was confirmed that the deodorant of the present invention and the SAP sheet for sanitary materials using the same have excellent deodorizing power for ammonia, hydrogen sulfide, trimethylamine and methylmercaptan.

Claims (3)

평균입도 0.2㎛ ~ 1.2 ㎛인 세라믹 콜로이드, 식물 추출 복합 발효물, 플로랄 워터, 천연방부제, 바인더 및 증점제를 혼합하여 혼합물을 준비하는 1단계;
상기 혼합물을 미분쇄 공정을 수행하여 미분쇄물을 수득하는 2단계; 및
상기 미분쇄물을 건조시켜서 분말을 수득하는 3단계;를 포함하되,
상기 1단계의 식물 추출 복합 발효물은 식물 추출 혼합물에 발효 여과물을 1 : 0.10 ~ 0.20 중량비로 접종 및 발효시킨 발효물로서, 병출 추출물 100 중량부에 대하여, 청호 추출물 60 ~ 100 중량부, 감초 추출물 60 ~ 100 중량부, 님잎 추출물 30 ~ 70 중량부, 컴프리잎 추출물 30 ~ 70 중량부 및 녹차 추출물 15 ~ 50 중량부을 포함하며,
상기 발효 여과물은 비피다 발효 여과물, 락토바실러스 발효 여과물 및 효모 발효 여과물을 포함하는 것을 특징으로 위생재용 소취제의 제조방법.
1 step of preparing a mixture by mixing ceramic colloids having an average particle size of 0.2 µm to 1.2 µm, plant-extracted complex fermented product, floral water, natural preservatives, binders, and thickeners;
A second step of obtaining a finely pulverized product by performing a fine pulverization process on the mixture; And
Including; 3 steps of drying the finely ground product to obtain a powder
The plant-extracted complex fermented product of step 1 is a fermented product obtained by inoculating and fermenting a fermented filtrate in a plant extract mixture at a weight ratio of 1: 0.10 to 0.20, and based on 100 parts by weight of the Byeongchul extract, 60 to 100 parts by weight of Cheongho extract, licorice 60 to 100 parts by weight of extract, 30 to 70 parts by weight of neem leaf extract, 30 to 70 parts by weight of comfrey leaf extract, and 15 to 50 parts by weight of green tea extract,
The fermentation filtrate comprises a Bifida fermentation filtrate, a lactobacillus fermentation filtrate, and a yeast fermentation filtrate.
평균입도 0.2㎛ ~ 1.2 ㎛인 세라믹 콜로이드, 식물 추출 복합 발효물, 플로랄 워터, 천연방부제, 바인더 및 증점제를 혼합하여 혼합물을 준비하는 1단계;
상기 혼합물을 미분쇄 공정을 수행하여 미분쇄물을 수득하는 2단계; 및
상기 미분쇄물을 건조시켜서 분말을 수득하는 3단계;를 포함하되,
상기 1단계의 상기 플로랄 워터는 병풀잎수 100 중량부에 대하여, 라벤더꽃수 0.05 ~ 5 중량부, 포트마리골드꽃수 0.05 ~ 5 중량부, 로즈마리수 0.05 ~ 3 중량부 및 녹차수 0.05 ~ 3 중량부를 포함하는 것을 특징으로 하는 위생재용 소취제의 제조방법.
1 step of preparing a mixture by mixing ceramic colloids having an average particle size of 0.2 µm to 1.2 µm, plant-extracted complex fermented product, floral water, natural preservatives, binders, and thickeners;
A second step of obtaining a finely pulverized product by performing a fine pulverization process on the mixture; And
Including; 3 steps of drying the finely ground product to obtain a powder
The floral water of the first step is 0.05 to 5 parts by weight of lavender flowers, 0.05 to 5 parts by weight of pot marigold flowers, 0.05 to 3 parts by weight of rosemary water, and 0.05 to 3 parts by weight of green tea water, based on 100 parts by weight of centella leaf number. Method for producing a deodorant for hygiene, characterized in that it comprises.
제1항 또는 제2항에 있어서, 상기 2단계의 미분쇄 공정은 유성 압연기(Planetary mill)를 이용하여 수행하며,
비드 직경 1.0 ~ 2.5 mm, 아웃터모터(outer motor) 500 ~ 800 rpm 및 이너모터(inner motor) 800 ~ 1000 rpm 조건 하에서 수행하는 것을 특징으로 하는 위생재용 소취제의 제조방법.
The method of claim 1 or 2, wherein the pulverization process of the second step is performed using a planetary mill,
Bead diameter 1.0 ~ 2.5 mm, outer motor (outer motor) 500 ~ 800 rpm, and inner motor (inner motor) 800 ~ 1000 rpm, characterized in that it is carried out under conditions for producing a deodorant for sanitary material.
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