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CN108728269B - A kind of super cleaning power nano coral calcium powder cleaning agent and preparation method thereof - Google Patents

A kind of super cleaning power nano coral calcium powder cleaning agent and preparation method thereof Download PDF

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CN108728269B
CN108728269B CN201810877156.6A CN201810877156A CN108728269B CN 108728269 B CN108728269 B CN 108728269B CN 201810877156 A CN201810877156 A CN 201810877156A CN 108728269 B CN108728269 B CN 108728269B
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calcium powder
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coral calcium
nano coral
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CN108728269A (en
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王文举
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Guangdong Longxing Tianxia Technology Co ltd
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Guandao Guangzhou Technology Co ltd
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    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
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Abstract

本发明提供一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;C组分:单宁;本发明提供的超強洗净力纳米珊瑚钙粉清洗剂可以轻松对付厨房中的重油污;能够快速分解油污,同时对分解后的油污进行吸附,方便清除。The invention provides a super cleaning power nano coral calcium powder cleaning agent. The preparation raw materials of the cleaning agent comprise: A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent; B component: Baibu extract, Phellodendron chinensis extract, Radix radish extract, Radix japonica extract; C component: tannin; the super cleaning power nano coral calcium powder cleaning agent provided by the present invention can easily deal with heavy oil stains in the kitchen; It can quickly decompose oil stains, and at the same time adsorb the decomposed oil stains for easy removal.

Description

一种超強洗净力纳米珊瑚钙粉清洗剂及其制备方法A kind of super cleaning power nano coral calcium powder cleaning agent and preparation method thereof

技术领域technical field

本发明涉及清洗剂,更加涉及厨房用清洗剂。The present invention relates to a cleaning agent, and more particularly to a kitchen cleaning agent.

背景技术Background technique

现实生活中,由于生活过程中的日积月累,使得家庭、宾馆、饭店等厨房里的卫生状况出现许多的死角,各个角落出现一些难以去除的污垢,这些常年积累下来的污垢,仅仅依靠普通清洗剂去污效果不强,难以实现快速、彻底的清洁,导致清洁过程费时费力,工作效率低,清洁效果不理想。In real life, due to the accumulation of life in the process of life, there are many dead corners in the sanitary conditions of households, hotels, restaurants and other kitchens, and there are some difficult-to-remove dirt in every corner. The pollution effect is not strong, and it is difficult to achieve fast and thorough cleaning, resulting in time-consuming and laborious cleaning process, low work efficiency, and unsatisfactory cleaning effect.

常规使用的厨房重油的清洗剂,其需要比较刺激的清洗成分,且其油污分解后的小分子油污不易擦除,且需要采用清洁球等钢丝球与其配合;同时擦除后的重油地方,后续还是会经历同样的过程才能重新干净。The conventionally used kitchen heavy oil cleaning agent requires relatively stimulating cleaning ingredients, and the small molecular oil stains after the oil stains are decomposed are not easy to remove, and steel balls such as cleaning balls need to be used to cooperate with them; Still going through the same process to get clean again.

针对上述问题,本发明提供一种超強洗净力纳米珊瑚钙粉清洗剂。In view of the above-mentioned problems, the present invention provides a super cleaning power nano coral calcium powder cleaning agent.

发明内容SUMMARY OF THE INVENTION

本发明提供一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:The invention provides a super cleaning power nano coral calcium powder cleaning agent, and the preparation raw materials of the cleaning agent comprise:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

作为本发明的一种实施方式,所述纳米珊瑚钙粉为多糖改性珊瑚钙粉。As an embodiment of the present invention, the nano coral calcium powder is polysaccharide modified coral calcium powder.

作为本发明的一种实施方式,所述多糖为果胶。As an embodiment of the present invention, the polysaccharide is pectin.

作为本发明的一种实施方式,所述单宁为水解类单宁。As an embodiment of the present invention, the tannins are hydrolyzed tannins.

作为本发明的一种实施方式,所述组分B通过缓释膜进行包覆。As an embodiment of the present invention, the component B is coated by a sustained-release film.

作为本发明的一种实施方式,所述缓释膜为改性鼠李糖。As an embodiment of the present invention, the sustained-release film is modified rhamnose.

作为本发明的一种实施方式,所述表面活性剂为非离子表面活性剂。As an embodiment of the present invention, the surfactant is a nonionic surfactant.

作为本发明的一种实施方式,按照重量份计,所述A组分和B组分的重量比为(1-3):1。As an embodiment of the present invention, in parts by weight, the weight ratio of the A component to the B component is (1-3):1.

作为本发明的一种实施方式,所述B组分的制备方法如下:As an embodiment of the present invention, the preparation method of the B component is as follows:

S01将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。S01 Dissolve 1.5 g of rhamnose in 100 mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1 g of polyvinyl alcohol in 30 mL of water, and heat it to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions evenly , 50 ℃ water bath for 48h, take 40mL of the mixed solution, add 1.6-2.8g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

S02取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;S02 get the extract mixture after mixing the H. chinensis extract, Phellodendron chinensis extract, Radix radish extract, and Radix chinensis extract;

S03取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。S03 take 10g of rhamnose/polyvinyl alcohol prepared in step 1 and mix with 80g of distilled water, and add 6g of the extract mixture at room temperature, stir evenly, ultrasonicate for 30min to make it evenly mixed, then at an inlet temperature of 175 ° C, feed flow rate Component B was obtained by spray drying under the conditions of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning 2 times/min.

作为本发明的一种实施方式,所述百部提取物和黄柏提取物的提取方法如下:As an embodiment of the present invention, the extraction methods of the Hundred Fructus extract and Phellodendron chinensis extract are as follows:

(1)选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;(1) Select 1 part of Hundred Roots and 1 part of Cork bark, wash, dry and pulverize, add 10 parts of lime milk and stir evenly, put it into a percolation cylinder and soak it in lime water for 6 hours, take the percolation 120% of the volume of the percolation solution was added, and a saturated aqueous solution of citric acid was added, stirred and then placed overnight, and the precipitate was collected by filtration;

(2)将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;(2) after dissolving the precipitation with hot water, filter while hot, get the filtrate, and then prepare the crude product of the extract of Phellodendron chinensis and Phellodendron chinensis;

(3)将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。(3) adding the crude product to boiling water and dissolving it, filtering while hot, and then preparing the extracts of Baibu and Phellodendron chinensis.

有益效果:Beneficial effects:

1.本发明提供的超強洗净力纳米珊瑚钙粉清洗剂可以轻松对付厨房中的重油污;能够快速分解油污,同时对分解后的油污进行吸附,方便清除;1. The super cleaning power nano coral calcium powder cleaning agent provided by the present invention can easily deal with heavy oil stains in the kitchen; it can quickly decompose the oil stains, and simultaneously adsorb the decomposed oil stains for easy removal;

2.本发明的超強洗净力纳米珊瑚钙粉清洗剂可以对清洗后的受污染表面形成一层保护膜,延长油污的污染周期。2. The super cleaning power nano coral calcium powder cleaning agent of the present invention can form a layer of protective film on the cleaned contaminated surface and prolong the pollution period of oil pollution.

具体实施方式Detailed ways

为了下面的详细描述的目的,应当理解,本发明可采用各种替代的变化和步骤顺序,除非明确规定相反。此外,除了在任何操作实例中,或者以其他方式指出的情况下,表示例如说明书和权利要求中使用的成分的量的所有数字应被理解为在所有情况下被术语“约”修饰。因此,除非相反指出,否则在以下说明书和所附权利要求中阐述的数值参数是根据本发明所要获得的期望性能而变化的近似值。至少并不是试图将等同原则的适用限制在权利要求的范围内,每个数值参数至少应该根据报告的有效数字的个数并通过应用普通舍入技术来解释。For the purposes of the following detailed description, it should be understood that the present invention may employ various alternative variations and sequences of steps, unless expressly stated to the contrary. Furthermore, except in any working example, or where otherwise indicated, all numbers expressing amounts of ingredients, eg, as used in the specification and claims, should be understood to be modified in all instances by the term "about." Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties to be obtained by the present invention. At least not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, but each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

尽管阐述本发明的广泛范围的数值范围和参数是近似值,但是具体实例中列出的数值尽可能精确地报告。然而,任何数值固有地包含由其各自测试测量中发现的标准偏差必然产生的某些误差。Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

此外,应当理解,本文所述的任何数值范围旨在包括归入其中的所有子范围。例如,“1至10”的范围旨在包括介于(并包括)所述最小值1和所述最大值10之间的所有子范围,即具有等于或大于1的最小值和等于或小于10的最大值。Furthermore, it should be understood that any numerical range recited herein is intended to include all subranges subsumed therein. For example, a range of "1 to 10" is intended to include (and include) all subranges between said minimum value of 1 and said maximum value of 10, ie having a minimum value equal to or greater than 1 and a minimum value equal to or less than 10 the maximum value of .

本发明提供一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:The invention provides a super cleaning power nano coral calcium powder cleaning agent, and the preparation raw materials of the cleaning agent comprise:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

A组分Component A

表面活性剂Surfactant

本发明中,所述表面活性剂为非离子表面活性剂和阴离子表面活性剂按照重量比为1:2的混合物。In the present invention, the surfactant is a mixture of a nonionic surfactant and an anionic surfactant in a weight ratio of 1:2.

非离子表面活性剂:本发明中所述非离子表面活性剂为聚氧乙烯型非离子表面活性剂;聚氧乙烯型非离子表面活性剂,是环氧乙烷与含有活泼氢的化合物进行加成反应的产物;所谓活泼氢原子是指-OH、-COOH、-NH2和-CONH2等基团中的氢原子。Nonionic surfactant: the nonionic surfactant described in the present invention is a polyoxyethylene type nonionic surfactant; a polyoxyethylene type nonionic surfactant is the addition of ethylene oxide and a compound containing active hydrogen. The so-called active hydrogen atom refers to the hydrogen atom in groups such as -OH, -COOH, -NH 2 and -CONH 2 .

作为本发明的一种实施方式,所述非离子表面活性剂选自吐温-20、吐温-60、吐温-80中的一种或多种。As an embodiment of the present invention, the nonionic surfactant is selected from one or more of Tween-20, Tween-60, and Tween-80.

阴离子表面活性剂:本发明中所述阴离子表面活性剂为十二烷基苯磺酸钠。Anionic surfactant: the anionic surfactant in the present invention is sodium dodecylbenzenesulfonate.

纳米珊瑚钙粉Nano coral calcium powder

珊瑚钙是日常营养补充品,它是活珊瑚经过风化与自然分解而成的珊瑚沙。它含有非常高浓度的钙质、主要矿物质与微量矿物质,因为矿物含量丰富,又被称为海洋钻石。Coral calcium is a daily nutritional supplement, which is coral sand formed by weathering and natural decomposition of living corals. It contains very high concentrations of calcium, major minerals and trace minerals, and is also known as ocean diamonds because of its abundance.

本发明的纳米珊瑚钙粉是将珊瑚钙进行研磨,研磨至纳米级别,然后进行多糖改性纳米珊瑚钙粉;所述多糖为果胶。In the nano coral calcium powder of the present invention, the coral calcium is ground to a nanometer level, and then the nano coral calcium powder is modified by polysaccharide; the polysaccharide is pectin.

本发明中,所述多糖改性纳米珊瑚钙粉的制备方法如下:In the present invention, the preparation method of the polysaccharide modified nano coral calcium powder is as follows:

1.在室温条件下,向纳米珊瑚钙粉中滴入少量的去离子水,并用超声波振荡处理后使其均匀分散;1. At room temperature, drop a small amount of deionized water into the nano coral calcium powder, and use ultrasonic vibration to make it evenly dispersed;

2.将多糖分散在水溶液中,制备成浓度为3%的多糖溶液;2. Disperse the polysaccharide in an aqueous solution to prepare a polysaccharide solution with a concentration of 3%;

3.在超声条件下,将多糖溶液逐渐滴入步骤1的纳米珊瑚钙粉浆液中,滴加完毕后,继续超声处理10分钟后,将混合液放入在零下80℃下冷冻12小时后,再经冷冻干燥即可制备得到多糖改性纳米珊瑚钙粉。3. Under ultrasonic conditions, gradually drop the polysaccharide solution into the nano coral calcium powder slurry in step 1. After the addition is completed, continue ultrasonic treatment for 10 minutes, and then put the mixture into freezing at minus 80 ° C for 12 hours. The polysaccharide modified nano coral calcium powder can be prepared by freeze-drying.

其中,多糖和纳米珊瑚钙粉的重量比为1:2。Among them, the weight ratio of polysaccharide and nano coral calcium powder is 1:2.

柠檬酸钠Sodium citrate

别名枸橼酸钠,是一种有机化合物,外观为白色到无色晶体。无臭,有清凉咸辣味。常温及空气中稳定,在湿空气中微有溶解性,在热空气中产生风化现象。加热至150℃失去结晶水。易溶于水、可溶于甘油、难溶于醇类及其他有机溶剂,过热分解,在潮湿的环境中微有潮解,在热空气中微有风化。Also known as sodium citrate, it is an organic compound with the appearance of white to colorless crystals. Odorless, with a cool salty and spicy taste. Stable at room temperature and air, slightly soluble in humid air, and weathering in hot air. Heated to 150 ℃ to lose crystal water. Easily soluble in water, soluble in glycerol, insoluble in alcohols and other organic solvents, decomposed by overheating, slightly deliquescence in humid environment, and slightly weathered in hot air.

螯合剂chelating agent

金属原子或离子与含有两个或两个以上配位原子的配位体作用,生成具有环状结构的络合物,该络合物叫做螯合物。能生成螯合物的这种配体物质叫螯合剂,也称为络合剂。Metal atoms or ions interact with ligands containing two or more coordinating atoms to form complexes with cyclic structures, which are called chelates. The ligand substances that can generate chelates are called chelating agents, also known as complexing agents.

本发明中所述螯合剂选自乙二胺四乙酸四钠、酒石酸钠、羟基乙叉二膦酸四钠和亚氨基二琥珀酸四钠中的一种或两种。In the present invention, the chelating agent is selected from one or two of tetrasodium ethylenediaminetetraacetate, sodium tartrate, tetrasodium hydroxyethylidene diphosphonate and tetrasodium iminodisuccinate.

作为本发明的一种实施方式,所述螯合剂为乙二胺四乙酸四钠。As an embodiment of the present invention, the chelating agent is tetrasodium EDTA.

B组分component B

本发明中,所述B组分为百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物,且所述B组分经过缓释膜包覆。In the present invention, the B component is a hundred parts extract, a Phellodendron chinensis extract, a Radix radish extract, and a cinnamon sage extract, and the B component is coated with a slow-release film.

所述缓释膜为改性鼠李糖,且所述改性鼠李糖为聚乙烯醇改性鼠李糖。The sustained-release film is modified rhamnose, and the modified rhamnose is polyvinyl alcohol modified rhamnose.

本发明中,所述组分B的制备方法如下:In the present invention, the preparation method of the component B is as follows:

S01.将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。S01. Dissolve 1.5 g of rhamnose in 100 mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1 g of polyvinyl alcohol in 30 mL of water, and heat it to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions Homogeneous, 50 ℃ water bath for 48 hours, take 40 mL of the mixed solution, add 1.6-2.8 g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

S02.取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;S02. Get the extract mixture after mixing the extracts of Phellodendron chinensis, Phellodendron chinensis, Radix Radix extract, and Echinensis chinensis extracts;

S03.取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。S03. get 10g of the rhamnose/polyvinyl alcohol prepared in step 1 and mix with 80g of distilled water, add 6g of the extract mixture at room temperature, stir evenly, ultrasonicate for 30min to make it evenly mixed, and then feed at an inlet temperature of 175° C. Component B was obtained by spray drying under the conditions of flow rate of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning twice/min.

百部提取物、黄柏提取物Baibu Extract, Phellodendron Extract

百部亦称婆妇草,药虱药,是百部科的植物。百部为多年生草本,地下簇生纺锤状肉质块根,茎上部攀援它物上升。卵形叶,2-4片轮生节上。初春开淡绿色花,花梗贴生于叶主脉上,像花从叶上长出一样。Baibu is also known as the mother-in-law grass, medicine for lice, and it is a plant of the family Babuaceae. Hundreds of plants are perennial herbs, with spindle-shaped fleshy roots clustered underground, and the upper part of the stem climbs and rises. Leaves ovate, on 2-4 whorls. Light green flowers bloom in early spring, and the pedicels are attached to the main veins of the leaves, like flowers growing from the leaves.

百部富含有大量的生物碱,根含百部碱、对叶百部碱、斯替宁碱、次百部碱、氧化百部碱;尚含糖2.32%,脂类0.84%,蛋白质9.25%,灰分12.1%,以及乙酸、甲酸、苹果酸、琥珀酸、草酸等。Baibu is rich in a large amount of alkaloids, the root contains 100 alkaloids, 100 alkaloids, stinine alkaloids, 100 alkaloids, 100 alkaloids; still contains 2.32% sugar, 0.84% lipids, and 9.25% protein %, ash 12.1%, and acetic acid, formic acid, malic acid, succinic acid, oxalic acid, etc.

黄柏树皮含小檗碱、药根碱、木兰花碱、黄柏碱、N-甲基大麦芽碱、掌叶防己碱、蝙蝠葛碱等生物碱;另含黄柏酮、黄柏内酯、白鲜交酯、黄柏酮酸、青萤光酸、7-脱氢豆甾醇、β-谷甾醇、菜油甾醇。根皮含小檗碱、药根碱、黄柏碱、N-甲基大麦芽碱。木材也含小檗碱。新鲜叶含黄柏甙、脱氢黄柏甙、脱氢异黄柏甙、异黄柏甙。干燥叶含金丝桃甙,不含黄柏甙。Phellodendron bark contains alkaloids such as berberine, jatrorrhizine, magnolidine, phellodendron, N-methylhordeline, tetrandrine, kudzurine; also contains phellodendron, phellodendron lactone, white fresh Lactide, yellow ketone acid, cyanofluoric acid, 7-dehydrostigmasterol, beta-sitosterol, campesterol. The root bark contains berberine, jatrorrhizine, phellodendron, and N-methylhordeline. Wood also contains berberine. Fresh leaves contain phellodendron, dehydrophellodendri, dehydroisoopterin, and isofokin. Dried leaves contain hypericin but not phellodendron.

本发明中,所述百部提取物和黄柏提取物的提取方法如下:In the present invention, the extracting methods of the Hundred Blossoms extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 120% of the volume of the percolation solution, add saturated aqueous citric acid, stir, place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;2. After dissolving the precipitation with hot water, filter it while hot, and take the filtrate to prepare the crude product of Baibu extract and Phellodendron chinensis extract;

3.将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。3. Add the crude product to boiling water to dissolve, filter while hot, and then prepare the extract of Baibu and Phellodendron chinensis.

本发明中,常规百部提取物和黄柏提取物是分开提取的,同时常规的提取中加入石灰乳后加入的是碱性物质,本发明中加入过量的有机酸,可以减去后期再加入盐酸进行pH调节,从而可以获取百部提取物和黄柏提取物的除小檗碱和百部碱之外的木兰花碱、黄柏碱等生物碱,避免过多的物质损失。In the present invention, the conventional H. chinensis extract and the Phellodendron chinensis extract are extracted separately, and at the same time in the conventional extraction, what is added after adding the milk of lime is an alkaline substance. In the present invention, adding an excessive amount of organic acid can reduce the addition of hydrochloric acid at a later stage. The pH adjustment is carried out, so that alkaloids such as magnolidine and phellodendron alkaloids other than berberine and phellodendron alkaloids in the extract and Phellodendron chinensis extract can be obtained, so as to avoid excessive material loss.

莱菔子提取物Raisin Seed Extract

莱菔子,中药名。为十字花科植物萝卜的干燥成熟种子。夏季果实成熟时采割植株,晒干,搓出种子,除去杂质,再晒干。Raisin, Chinese medicine name. It is the dry ripe seed of cruciferous radish. In summer, when the fruit is ripe, the plants are harvested, dried in the sun, the seeds are rubbed out, impurities are removed, and then dried in the sun.

其化学成分,种子含脂肪油、挥发油。挥发油内有甲硫醇等。脂肪油中含多量芥酸、亚油酸、亚麻酸以及芥子酸甘油酯等。尚含有抗菌物质称莱菔素。Its chemical composition, the seeds contain fatty oil and volatile oil. There are methyl mercaptan in the volatile oil. Fatty oils contain a lot of erucic acid, linoleic acid, linolenic acid, and glyceryl sinapic acid. It still contains an antibacterial substance called rapin.

本发明中,所述莱菔子提取物的制备方法参考专利CN103830305A的制备方法。In the present invention, the preparation method of the radish seed extract refers to the preparation method of the patent CN103830305A.

茵陈提取物cinnamon extract

含挥发油,油中成分有香芹酮、对-聚伞花素、苎烯、紫苏烯、α-水芹烯、百里香酚、α-、β-β-蒎烯、松油醇-4、马鞭草酮、萘、芳甲基苯乙酮.另含滨蒿素、对羟基苯乙酮及绿原酸等.菌陈含挥发油,油中成分有月桂烯、苎烯、桉油精、α-蒎烯、莰烯、α-姜黄烯、达瓦酮、茵陈炔酮、丁香酚、异丁香酚、萘、苯甲醛、龙脑。另含茵陈色原酮、6,7-二甲氧基香豆素。Contains volatile oil, the ingredients in the oil are carvone, p-cymene, limonene, perillene, α-phellandrene, thymol, α-, β-β-pinene, terpineol-4, Verbenone, naphthalene, aryl methyl acetophenone. Also contains amaranthine, p-hydroxyacetophenone and chlorogenic acid, etc. Bacteria contain volatile oil, and the components in the oil are myrcene, limonene, eucalyptol, alpha -Pinene, camphene, alpha-curcumene, darvalone, entrenone, eugenol, isoeugenol, naphthalene, benzaldehyde, borneol. In addition, it contains chromogen ketone and 6,7-dimethoxycoumarin.

本发明中,所述茵陈提取物的制备方法如下:In the present invention, the preparation method of described Radix japonica extract is as follows:

1.选取茵陈10份,用水煎煮4小时后,过滤,得水提液;1. Select 10 parts of Yin Chen, decoct with water for 4 hours, and filter to obtain a water extract;

2.然后将水提液浓缩至1/4体积后,用氯仿萃取;2. After concentrating the aqueous extract to 1/4 volume, extract with chloroform;

3.选取氯仿萃取液,然后分别用5%碳酸氢钠和2%氢氧化钠萃取,选取氢氧化钠提取液后,用盐酸酸化后,继续用氯仿提取;3. Select the chloroform extract, then extract with 5% sodium bicarbonate and 2% sodium hydroxide respectively, select the sodium hydroxide extract, acidify with hydrochloric acid, and continue to extract with chloroform;

4.选取氯仿提取液,回收氯仿后,将酸性部分经聚酰胺柱层析,用乙醇(浓度分别为30%、50%和80%)梯度洗脱;4. Select the chloroform extract, and after recovering the chloroform, the acidic part is subjected to polyamide column chromatography and eluted with a gradient of ethanol (concentrations are 30%, 50% and 80%, respectively);

5.选取80%浓度乙醇洗脱部位,然后加热挥发乙醇,用乙醚萃取后,回收乙醚萃取液,回收乙醚,得到白色固体,即可制备得到茵陈提取物。5. Select the elution part of 80% concentration ethanol, then heat to volatilize the ethanol, extract with ether, recover the ether extract, recover the ether to obtain a white solid, and then prepare the cypress extract.

C组分C component

本发明中,所述单宁为水解类单宁,本发明中所述水解类单宁为五棓子酸。In the present invention, the tannins are hydrolyzed tannins, and the hydrolyzed tannins in the present invention are gallic acid.

作为本发明的一种实施方式,按照重量份计,所述A组分、B组分和C组分的重量比为8:4:1。As an embodiment of the present invention, in parts by weight, the weight ratio of the A component, the B component and the C component is 8:4:1.

A组分中,所述表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂的重量比为1:1:0.5:0.01。In component A, the weight ratio of the surfactant, nano coral calcium powder, sodium citrate and chelating agent is 1:1:0.5:0.01.

B组分中,所述百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物的重量比为1:1:1:1。In the B component, the weight ratio of the Hundred Fructus extract, Phellodendron chinensis extract, Radix Rhizoma extract, and Echinensis chinensis extract is 1:1:1:1.

本发明提供的所述超強洗净力纳米珊瑚钙粉清洗剂,其在包装中,分别独立包装,使用时再混合。The super cleaning power nano coral calcium powder cleaning agent provided by the present invention is separately packaged in the package, and then mixed when used.

机理解释:常规使用的厨房重油的清洗剂,其需要比较刺激的清洗成分,且其油污分解后的小分子油污不易擦除,且需要采用清洁球等钢丝球与其配合;同时擦除后的重油地方,后续还是会经历同样的过程才能重新干净。本发明提供的超強洗净力纳米珊瑚钙粉清洗剂为固体粉末状,使用时可以对油污进行较强的分解和吸附作用,同时由于珊瑚钙粉经过处理对油污的吸附力增强,同时不会对待清洁表面造成划痕,同时结合缓释剂对待清洁表面形成保护膜,缓解油污的再次污染的周期。Mechanism explanation: The conventionally used kitchen heavy oil cleaning agent requires relatively stimulating cleaning ingredients, and the small molecular oil stains after the oil stains are decomposed are not easy to erase, and steel balls such as cleaning balls need to be used to cooperate with them; The place will go through the same process in the future to be cleaned again. The super cleaning power nano coral calcium powder cleaning agent provided by the present invention is in solid powder form, and can perform strong decomposition and adsorption on oil stains when in use. It will cause scratches on the surface to be cleaned, and at the same time, combined with the slow-release agent to form a protective film on the surface to be cleaned, it will alleviate the cycle of re-pollution of oil stains.

下面结合具体实施例对本发明提供的超強洗净力纳米珊瑚钙粉清洗剂进行详细说明。Below in conjunction with specific embodiments, the super cleaning power nano coral calcium powder cleaning agent provided by the present invention will be described in detail.

实施例1:Example 1:

一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:A kind of super cleaning power nano coral calcium powder cleaning agent, the preparation raw material of described cleaning agent comprises:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

所述表面活性剂为吐温-60和十二烷基苯磺酸钠按照重量比为1:2的混合物。The surfactant is a mixture of Tween-60 and sodium dodecylbenzenesulfonate in a weight ratio of 1:2.

所述多糖改性纳米珊瑚钙粉的制备方法如下:The preparation method of described polysaccharide modified nano coral calcium powder is as follows:

1.在室温条件下,向纳米珊瑚钙粉中滴入少量的去离子水,并用超声波振荡处理后使其均匀分散;1. At room temperature, drop a small amount of deionized water into the nano coral calcium powder, and use ultrasonic vibration to make it evenly dispersed;

2.将多糖分散在水溶液中,制备成浓度为3%的多糖溶液;2. Disperse the polysaccharide in an aqueous solution to prepare a polysaccharide solution with a concentration of 3%;

3.在超声条件下,将多糖溶液逐渐滴入步骤1的纳米珊瑚钙粉浆液中,滴加完毕后,继续超声处理10分钟后,将混合液放入在零下80℃下冷冻12小时后,再经冷冻干燥即可制备得到多糖改性纳米珊瑚钙粉。3. Under ultrasonic conditions, gradually drop the polysaccharide solution into the nano coral calcium powder slurry in step 1. After the addition is completed, continue ultrasonic treatment for 10 minutes, and then put the mixture into freezing at minus 80 ° C for 12 hours. The polysaccharide modified nano coral calcium powder can be prepared by freeze-drying.

其中,多糖和纳米珊瑚钙粉的重量比为1:2。Among them, the weight ratio of polysaccharide and nano coral calcium powder is 1:2.

所述螯合剂为乙二胺四乙酸四钠。The chelating agent is tetrasodium EDTA.

所述组分B的制备方法如下:The preparation method of described component B is as follows:

S01.将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。S01. Dissolve 1.5 g of rhamnose in 100 mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1 g of polyvinyl alcohol in 30 mL of water, and heat it to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions Homogeneous, 50 ℃ water bath for 48 hours, take 40 mL of the mixed solution, add 1.6-2.8 g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

S02.取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;S02. Get the extract mixture after mixing the extracts of Phellodendron chinensis, Phellodendron chinensis, Radix Radix extract, and Echinensis chinensis extracts;

S03.取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。S03. get 10g of the rhamnose/polyvinyl alcohol prepared in step 1 and mix with 80g of distilled water, add 6g of the extract mixture at room temperature, stir evenly, ultrasonicate for 30min to make it evenly mixed, and then feed at an inlet temperature of 175° C. Component B was obtained by spray drying under the conditions of flow rate of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning twice/min.

所述百部提取物和黄柏提取物的提取方法如下:The extracting methods of the Baibu extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 120% of the volume of the percolation solution, add saturated aqueous citric acid, stir, place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;2. After dissolving the precipitation with hot water, filter it while hot, and take the filtrate to prepare the crude product of Baibu extract and Phellodendron chinensis extract;

3.将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。3. Add the crude product to boiling water to dissolve, filter while hot, and then prepare the extract of Baibu and Phellodendron chinensis.

所述茵陈提取物的制备方法如下:The preparation method of the saffron extract is as follows:

1.选取茵陈10份,用水煎煮4小时后,过滤,得水提液;1. Select 10 parts of Yin Chen, decoct with water for 4 hours, and filter to obtain a water extract;

2.然后将水提液浓缩至1/4体积后,用氯仿萃取;2. After concentrating the aqueous extract to 1/4 volume, extract with chloroform;

3.选取氯仿萃取液,然后分别用5%碳酸氢钠和2%氢氧化钠萃取,选取氢氧化钠提取液后,用盐酸酸化后,继续用氯仿提取;3. Select the chloroform extract, then extract with 5% sodium bicarbonate and 2% sodium hydroxide respectively, select the sodium hydroxide extract, acidify with hydrochloric acid, and continue to extract with chloroform;

4.选取氯仿提取液,回收氯仿后,将酸性部分经聚酰胺柱层析,用乙醇(浓度分别为30%、50%和80%)梯度洗脱;4. Select the chloroform extract, and after recovering the chloroform, the acidic part is subjected to polyamide column chromatography and eluted with a gradient of ethanol (concentrations are 30%, 50% and 80%, respectively);

5.选取80%浓度乙醇洗脱部位,然后加热挥发乙醇,用乙醚萃取后,回收乙醚萃取液,回收乙醚,得到白色固体,即可制备得到茵陈提取物。5. Select the elution part of 80% concentration ethanol, then heat to volatilize the ethanol, extract with ether, recover the ether extract, recover the ether to obtain a white solid, and then prepare the cypress extract.

所述单宁为五棓子酸。The tannin is gallic acid.

所述A组分、B组分和C组分的重量比为8:4:1。The weight ratio of the A component, the B component and the C component is 8:4:1.

A组分中,所述表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂的重量比为1:1:0.5:0.01。In component A, the weight ratio of the surfactant, nano coral calcium powder, sodium citrate and chelating agent is 1:1:0.5:0.01.

B组分中,所述百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物的重量比为1:1:1:1。In the B component, the weight ratio of the Hundred Fructus extract, Phellodendron chinensis extract, Radix Rhizoma extract, and Echinensis chinensis extract is 1:1:1:1.

实施例2:Example 2:

一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:A kind of super cleaning power nano coral calcium powder cleaning agent, the preparation raw material of described cleaning agent comprises:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

所述表面活性剂为吐温-60和十二烷基苯磺酸钠按照重量比为1:1的混合物。The surfactant is a mixture of Tween-60 and sodium dodecylbenzenesulfonate in a weight ratio of 1:1.

所述多糖改性纳米珊瑚钙粉的制备方法如下:The preparation method of described polysaccharide modified nano coral calcium powder is as follows:

1.在室温条件下,向纳米珊瑚钙粉中滴入少量的去离子水,并用超声波振荡处理后使其均匀分散;1. At room temperature, drop a small amount of deionized water into the nano coral calcium powder, and use ultrasonic vibration to make it evenly dispersed;

2.将多糖分散在水溶液中,制备成浓度为3%的多糖溶液;2. Disperse the polysaccharide in an aqueous solution to prepare a polysaccharide solution with a concentration of 3%;

3.在超声条件下,将多糖溶液逐渐滴入步骤1的纳米珊瑚钙粉浆液中,滴加完毕后,继续超声处理10分钟后,将混合液放入在零下80℃下冷冻12小时后,再经冷冻干燥即可制备得到多糖改性纳米珊瑚钙粉。3. Under ultrasonic conditions, gradually drop the polysaccharide solution into the nano coral calcium powder slurry in step 1. After the addition is completed, continue ultrasonic treatment for 10 minutes, and then put the mixture into freezing at minus 80 ° C for 12 hours. The polysaccharide modified nano coral calcium powder can be prepared by freeze-drying.

其中,多糖和纳米珊瑚钙粉的重量比为1:1。Among them, the weight ratio of polysaccharide and nano coral calcium powder is 1:1.

所述螯合剂为乙二胺四乙酸四钠。The chelating agent is tetrasodium EDTA.

所述组分B的制备方法如下:The preparation method of described component B is as follows:

1.将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。1. Dissolve 1.5g of rhamnose in 100mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1g of polyvinyl alcohol in 30mL of water, heat to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions Homogeneous, 50 ℃ water bath for 48 hours, take 40 mL of the mixed solution, add 1.6-2.8 g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

2.取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;2. Get the extract mixture after taking the Hundred Bulb extract, Phellodendron chinensis extract, Radix Phellodendri extract, and Echinensis chinensis extract and mixing;

3.取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。3. Mix 10 g of rhamnose/polyvinyl alcohol prepared in step 1 with 80 g of distilled water, add 6 g of the extract mixture at room temperature, stir evenly, sonicate for 30 min to make it evenly mixed, and then feed the mixture at an inlet temperature of 175° C. Component B was obtained by spray drying under the conditions of flow rate of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning twice/min.

所述百部提取物和黄柏提取物的提取方法如下:The extracting methods of the Baibu extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 120% of the volume of the percolation solution, add saturated aqueous citric acid, stir, place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;2. After dissolving the precipitation with hot water, filter it while hot, and take the filtrate to prepare the crude product of Baibu extract and Phellodendron chinensis extract;

3.将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。3. Add the crude product to boiling water to dissolve, filter while hot, and then prepare the extract of Baibu and Phellodendron chinensis.

所述茵陈提取物的制备方法如下:The preparation method of the saffron extract is as follows:

1.选取茵陈10份,用水煎煮4小时后,过滤,得水提液;1. Select 10 parts of Yin Chen, decoct with water for 4 hours, and filter to obtain a water extract;

2.然后将水提液浓缩至1/4体积后,用氯仿萃取;2. After concentrating the aqueous extract to 1/4 volume, extract with chloroform;

3.选取氯仿萃取液,然后分别用5%碳酸氢钠和2%氢氧化钠萃取,选取氢氧化钠提取液后,用盐酸酸化后,继续用氯仿提取;3. Select the chloroform extract, then extract with 5% sodium bicarbonate and 2% sodium hydroxide respectively, select the sodium hydroxide extract, acidify with hydrochloric acid, and continue to extract with chloroform;

4.选取氯仿提取液,回收氯仿后,将酸性部分经聚酰胺柱层析,用乙醇(浓度分别为30%、50%和80%)梯度洗脱;4. Select the chloroform extract, and after recovering the chloroform, the acidic part is subjected to polyamide column chromatography and eluted with a gradient of ethanol (concentrations are 30%, 50% and 80%, respectively);

5.选取80%浓度乙醇洗脱部位,然后加热挥发乙醇,用乙醚萃取后,回收乙醚萃取液,回收乙醚,得到白色固体,即可制备得到茵陈提取物。5. Select the elution part of 80% concentration ethanol, then heat to volatilize the ethanol, extract with ether, recover the ether extract, recover the ether to obtain a white solid, and then prepare the cypress extract.

所述单宁为五棓子酸。The tannin is gallic acid.

所述A组分、B组分和C组分的重量比为8:1:1。The weight ratio of the A component, the B component and the C component is 8:1:1.

A组分中,所述表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂的重量比为1:1:0.5:0.01。In component A, the weight ratio of the surfactant, nano coral calcium powder, sodium citrate and chelating agent is 1:1:0.5:0.01.

B组分中,所述百部提取物、莱菔子提取物、茵陈提取物的重量比为1:1:1。In the B component, the weight ratio of the Hundred Fructus extract, the Radix radish extract, and the Radix japonica extract is 1:1:1.

实施例3:Example 3:

一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:A kind of super cleaning power nano coral calcium powder cleaning agent, the preparation raw material of described cleaning agent comprises:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

所述表面活性剂为吐温-60和十二烷基苯磺酸钠按照重量比为1:2的混合物。The surfactant is a mixture of Tween-60 and sodium dodecylbenzenesulfonate in a weight ratio of 1:2.

所述多糖改性纳米珊瑚钙粉的制备方法如下:The preparation method of described polysaccharide modified nano coral calcium powder is as follows:

1.在室温条件下,向纳米珊瑚钙粉中滴入少量的去离子水,并用超声波振荡处理后使其均匀分散;1. At room temperature, drop a small amount of deionized water into the nano coral calcium powder, and use ultrasonic vibration to make it evenly dispersed;

2.将多糖分散在水溶液中,制备成浓度为3%的多糖溶液;2. Disperse the polysaccharide in an aqueous solution to prepare a polysaccharide solution with a concentration of 3%;

3.在超声条件下,将多糖溶液逐渐滴入步骤1的纳米珊瑚钙粉浆液中,滴加完毕后,继续超声处理10分钟后,将混合液放入在零下80℃下冷冻12小时后,再经冷冻干燥即可制备得到多糖改性纳米珊瑚钙粉。3. Under ultrasonic conditions, gradually drop the polysaccharide solution into the nano coral calcium powder slurry in step 1. After the addition is completed, continue ultrasonic treatment for 10 minutes, and then put the mixture into freezing at minus 80 ° C for 12 hours. The polysaccharide modified nano coral calcium powder can be prepared by freeze-drying.

其中,多糖和纳米珊瑚钙粉的重量比为1:2。Among them, the weight ratio of polysaccharide and nano coral calcium powder is 1:2.

所述螯合剂为乙二胺四乙酸四钠。The chelating agent is tetrasodium EDTA.

所述组分B的制备方法如下:The preparation method of described component B is as follows:

1.将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。1. Dissolve 1.5g of rhamnose in 100mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1g of polyvinyl alcohol in 30mL of water, heat to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions Homogeneous, 50 ℃ water bath for 48 hours, take 40 mL of the mixed solution, add 1.6-2.8 g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

2.取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;2. Get the extract mixture after taking the Hundred Bulb extract, Phellodendron chinensis extract, Radix Phellodendri extract, and Echinensis chinensis extract and mixing;

3.取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。3. Mix 10 g of rhamnose/polyvinyl alcohol prepared in step 1 with 80 g of distilled water, add 6 g of the extract mixture at room temperature, stir evenly, sonicate for 30 min to make it evenly mixed, and then feed the mixture at an inlet temperature of 175° C. Component B was obtained by spray drying under the conditions of flow rate of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning twice/min.

所述百部提取物和黄柏提取物的提取方法如下:The extracting methods of the Baibu extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 120% of the volume of the percolation solution, add saturated aqueous citric acid, stir, place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;2. After dissolving the precipitation with hot water, filter it while hot, and take the filtrate to prepare the crude product of Baibu extract and Phellodendron chinensis extract;

3.将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。3. Add the crude product to boiling water to dissolve, filter while hot, and then prepare the extract of Baibu and Phellodendron chinensis.

所述茵陈提取物的制备方法如下:The preparation method of the saffron extract is as follows:

1.选取茵陈10份,用水煎煮4小时后,过滤,得水提液;1. Select 10 parts of Yin Chen, decoct with water for 4 hours, and filter to obtain a water extract;

2.然后将水提液浓缩至1/4体积后,用氯仿萃取;2. After concentrating the aqueous extract to 1/4 volume, extract with chloroform;

3.选取氯仿萃取液,然后分别用5%碳酸氢钠和2%氢氧化钠萃取,选取氢氧化钠提取液后,用盐酸酸化后,继续用氯仿提取;3. Select the chloroform extract, then extract with 5% sodium bicarbonate and 2% sodium hydroxide respectively, select the sodium hydroxide extract, acidify with hydrochloric acid, and continue to extract with chloroform;

4.选取氯仿提取液,回收氯仿后,将酸性部分经聚酰胺柱层析,用乙醇(浓度分别为30%、50%和80%)梯度洗脱;4. Select the chloroform extract, and after recovering the chloroform, the acidic part is subjected to polyamide column chromatography and eluted with a gradient of ethanol (concentrations are 30%, 50% and 80%, respectively);

5.选取80%浓度乙醇洗脱部位,然后加热挥发乙醇,用乙醚萃取后,回收乙醚萃取液,回收乙醚,得到白色固体,即可制备得到茵陈提取物。5. Select the elution part of 80% concentration ethanol, then heat to volatilize the ethanol, extract with ether, recover the ether extract, recover the ether to obtain a white solid, and then prepare the cypress extract.

所述单宁为五棓子酸。The tannin is gallic acid.

所述A组分、B组分和C组分的重量比为8:8:1。The weight ratio of the A component, the B component and the C component is 8:8:1.

A组分中,所述表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂的重量比为1:1:0.5:0.01。In component A, the weight ratio of the surfactant, nano coral calcium powder, sodium citrate and chelating agent is 1:1:0.5:0.01.

B组分中,所述百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物的重量比为1:1:1:1。In the B component, the weight ratio of the Hundred Fructus extract, Phellodendron chinensis extract, Radix Rhizoma extract, and Echinensis chinensis extract is 1:1:1:1.

实施例4:Example 4:

一种超強洗净力纳米珊瑚钙粉清洗剂,所述清洗剂的制备原料包含:A kind of super cleaning power nano coral calcium powder cleaning agent, the preparation raw material of described cleaning agent comprises:

A组分:表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂;A component: surfactant, nano coral calcium powder, sodium citrate, chelating agent;

B组分:百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物;Component B: Baibu Extract, Phellodendron Root Extract, Raisin Seed Extract, Radix Cinnamon Extract;

C组分:单宁。Component C: Tannins.

所述表面活性剂为吐温-60和十二烷基苯磺酸钠按照重量比为1:2的混合物。The surfactant is a mixture of Tween-60 and sodium dodecylbenzenesulfonate in a weight ratio of 1:2.

所述多糖改性纳米珊瑚钙粉的制备方法如下:The preparation method of described polysaccharide modified nano coral calcium powder is as follows:

1.在室温条件下,向纳米珊瑚钙粉中滴入少量的去离子水,并用超声波振荡处理后使其均匀分散;1. At room temperature, drop a small amount of deionized water into the nano coral calcium powder, and use ultrasonic vibration to make it evenly dispersed;

2.将多糖分散在水溶液中,制备成浓度为3%的多糖溶液;2. Disperse the polysaccharide in an aqueous solution to prepare a polysaccharide solution with a concentration of 3%;

3.在超声条件下,将多糖溶液逐渐滴入步骤1的纳米珊瑚钙粉浆液中,滴加完毕后,继续超声处理10分钟后,将混合液放入在零下80℃下冷冻12小时后,再经冷冻干燥即可制备得到多糖改性纳米珊瑚钙粉。3. Under ultrasonic conditions, gradually drop the polysaccharide solution into the nano coral calcium powder slurry in step 1. After the addition is completed, continue ultrasonic treatment for 10 minutes, and then put the mixture into freezing at minus 80 ° C for 12 hours. The polysaccharide modified nano coral calcium powder can be prepared by freeze-drying.

其中,多糖和纳米珊瑚钙粉的重量比为1:2。Among them, the weight ratio of polysaccharide and nano coral calcium powder is 1:2.

所述螯合剂为乙二胺四乙酸四钠。The chelating agent is tetrasodium EDTA.

所述组分B的制备方法如下:The preparation method of described component B is as follows:

1.将1.5g鼠李糖溶于100mL 2%的乙酸水溶液中,磁力搅拌器搅拌溶解;1g聚乙烯醇溶于30mL水中,加热使其溶解;将上述鼠李糖、聚乙烯醇溶液搅拌混合均匀,50℃水浴48h,取40mL混合溶液加入200-300目的硅胶1.6-2.8g倒入玻璃平板,室温蒸发成膜。得到干燥的膜浸入2mol/L的氢氧化钠溶液,50℃水浴2h溶解硅胶,制得鼠李糖/聚乙烯醇。用5%的乙酸中和多余的氢氧化钠,去离子水冲洗至中性,干燥箱中干燥。1. Dissolve 1.5g of rhamnose in 100mL of 2% acetic acid aqueous solution, stir and dissolve with a magnetic stirrer; dissolve 1g of polyvinyl alcohol in 30mL of water, heat to dissolve; stir and mix the above rhamnose and polyvinyl alcohol solutions Homogeneous, 50 ℃ water bath for 48 hours, take 40 mL of the mixed solution, add 1.6-2.8 g of 200-300 mesh silica gel, pour it into a glass plate, and evaporate at room temperature to form a film. The obtained dried membrane was immersed in 2 mol/L sodium hydroxide solution, and the silica gel was dissolved in a water bath at 50 °C for 2 h to obtain rhamnose/polyvinyl alcohol. Neutralize excess sodium hydroxide with 5% acetic acid, rinse with deionized water until neutral, and dry in a dry box.

2.取百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物混合后,得到提取物混合物;2. Get the extract mixture after taking the Hundred Bulb extract, Phellodendron chinensis extract, Radix Phellodendri extract, and Echinensis chinensis extract and mixing;

3.取10g步骤1制备得到的鼠李糖/聚乙烯醇和80g蒸馏水混合,并于室温下加入6g提取物混合物,搅拌均匀,超声30min,使其混合均匀,然后于入口温度175℃、进料流量3mL/min、喷嘴头直径0.7mm和喷嘴清洗2次/min条件下进行喷雾干燥,得到组分B。3. Mix 10 g of rhamnose/polyvinyl alcohol prepared in step 1 with 80 g of distilled water, add 6 g of the extract mixture at room temperature, stir evenly, sonicate for 30 min to make it evenly mixed, and then feed the mixture at an inlet temperature of 175° C. Component B was obtained by spray drying under the conditions of flow rate of 3 mL/min, nozzle head diameter of 0.7 mm and nozzle cleaning twice/min.

所述百部提取物和黄柏提取物的提取方法如下:The extracting methods of the Baibu extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积120%加入枸椽酸饱和水溶液,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 120% of the volume of the percolation solution, add saturated aqueous citric acid, stir, place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,即可制备得到百部提取物和黄柏提取物粗品;2. After dissolving the precipitation with hot water, filter it while hot, and take the filtrate to prepare the crude product of Baibu extract and Phellodendron chinensis extract;

3.将粗品加入到沸水中溶解后趁热过滤,即可制备得到百部提取物和黄柏提取物。3. Add the crude product to boiling water to dissolve, filter while hot, and then prepare the extract of Baibu and Phellodendron chinensis.

所述茵陈提取物的制备方法如下:The preparation method of the saffron extract is as follows:

1.选取茵陈10份,用水煎煮4小时后,过滤,得水提液;1. Select 10 parts of Yin Chen, decoct with water for 4 hours, and filter to obtain a water extract;

2.然后将水提液浓缩至1/4体积后,用氯仿萃取;2. After concentrating the aqueous extract to 1/4 volume, extract with chloroform;

3.选取氯仿萃取液,然后分别用5%碳酸氢钠和2%氢氧化钠萃取,选取氢氧化钠提取液后,用盐酸酸化后,继续用氯仿提取;3. Select the chloroform extract, then extract with 5% sodium bicarbonate and 2% sodium hydroxide respectively, select the sodium hydroxide extract, acidify with hydrochloric acid, and continue to extract with chloroform;

4.选取氯仿提取液,回收氯仿后,将酸性部分经聚酰胺柱层析,用乙醇(浓度分别为30%、50%和80%)梯度洗脱;4. Select the chloroform extract, and after recovering the chloroform, the acidic part is subjected to polyamide column chromatography and eluted with a gradient of ethanol (concentrations are 30%, 50% and 80%, respectively);

5.选取80%浓度乙醇洗脱部位,然后加热挥发乙醇,用乙醚萃取后,回收乙醚萃取液,回收乙醚,得到白色固体,即可制备得到茵陈提取物。5. Select the elution part of 80% concentration ethanol, then heat to volatilize the ethanol, extract with ether, recover the ether extract, recover the ether to obtain a white solid, and then prepare the cypress extract.

所述单宁为五棓子酸。The tannin is gallic acid.

所述A组分、B组分和C组分的重量比为1:1:1。The weight ratio of the A component, the B component and the C component is 1:1:1.

A组分中,所述表面活性剂、纳米珊瑚钙粉、柠檬酸钠、螯合剂的重量比为1:1:0.5:0.01。In component A, the weight ratio of the surfactant, nano coral calcium powder, sodium citrate and chelating agent is 1:1:0.5:0.01.

B组分中,所述百部提取物、黄柏提取物、莱菔子提取物、茵陈提取物的重量比为1:1:1:1。In the B component, the weight ratio of the Hundred Fructus extract, Phellodendron chinensis extract, Radix Rhizoma extract, and Echinensis chinensis extract is 1:1:1:1.

实施例5:实施例5的具体实施方式同实施例1,不同之处,所述纳米珊瑚钙粉未经过改性。Example 5: The specific implementation of Example 5 is the same as Example 1, except that the nano coral calcium powder is not modified.

实施例6:实施例6的具体实施方式同实施例1,不同之处,所述组分B未经过缓释膜包覆。Example 6: The specific implementation of Example 6 is the same as that of Example 1, except that the component B is not coated with a sustained-release film.

实施例7:实施例7的具体实施方式同实施例1,不同之处,所述百部提取物和黄柏提取物的提取方法如下:Example 7: The specific implementation of Example 7 is the same as Example 1, and the difference is that the extraction methods of the Hundred Blossoms extract and Phellodendron chinensis extract are as follows:

1.选取1份百部根部和1份黄柏树皮,洗净,烘干研碎后,加入10份石灰乳搅拌均匀后,放入渗漉筒内用石灰水浸泡6小时后,取渗漉液,加入渗漉液体积7%加入氯化钠,搅拌后放置过夜,过滤取沉淀;1. Select 1 part of Hundred Roots and 1 part of Phellodendron bark, wash, dry and grind, add 10 parts of lime milk and stir evenly, put it into the percolation cylinder and soak in lime water for 6 hours, take the percolation liquid, add 7% of the percolation solution by volume, add sodium chloride, stir and place overnight, and filter to get the precipitate;

2.将沉淀用热水溶解后,趁热过滤,取滤液,加盐酸调酸碱值为2,放置过夜,过滤取沉淀,2. After dissolving the precipitate with hot water, filter it while it is still hot, take the filtrate, add hydrochloric acid to adjust the pH value to 2, leave it overnight, and filter to get the precipitate.

3.将沉淀物水性至中性,抽干后,室温下烘干,即可制备得到粗品;3. Make the precipitate water-based to neutral, drain it, and dry it at room temperature to prepare the crude product;

4.将粗品加入到沸水中溶解后趁热过滤,取滤液,滴加浓盐酸至酸碱值为2,取沉淀,水洗至中性,即可得到精品。4. Add the crude product to boiling water to dissolve it, filter it while hot, take the filtrate, add concentrated hydrochloric acid dropwise until the pH value is 2, take the precipitate, wash it with water until it becomes neutral, and then the fine product can be obtained.

实施例8:实施例8的具体实施方式同实施例1,不同之处,所述A组分没有纳米珊瑚钙粉。Example 8: The specific implementation of Example 8 is the same as Example 1, except that the A component does not have nano coral calcium powder.

实施例9:实施例9的具体实施方式同实施例1,不同之处,所述清洗剂的制备原料无C组分。Example 9: The specific implementation of Example 9 is the same as that of Example 1, except that the preparation raw material of the cleaning agent has no C component.

实施例10:实施例10的具体实施方式同实施例1,不同之处,所述缓释膜为聚乙烯醇。Example 10: The specific implementation of Example 10 is the same as that of Example 1, except that the sustained-release film is polyvinyl alcohol.

性能测试Performance Testing

测试1:去污力测试:Test 1: Detergency Test:

1)人工污垢的制备1) Preparation of artificial dirt

混合油配方:以牛油、猪油、植物油质量比为0.5:0.5:1配制,并加入其总质量5%的单硬脂酸甘油酯,此即为人工污垢。Mixed oil formula: The mass ratio of tallow, lard, and vegetable oil is 0.5:0.5:1, and 5% of the total mass of glycerol monostearate is added, which is artificial dirt.

将人工污垢置电炉上加热至180℃,搅拌保持此温度10min,将烧杯移至电磁搅拌器搅拌,自然冷却至所需温度备用。涂污温度推荐参考:当室温为20℃时,需油温80℃;室温为25℃时,需油温45℃;当室温低于17℃或高于27℃时,试验不宜进行,需要在空调间进行。必要时应使用附冷冻装置的立式去污机。Put the artificial dirt on an electric furnace and heat it to 180°C, keep stirring at this temperature for 10 minutes, move the beaker to an electromagnetic stirrer for stirring, and naturally cool to the required temperature for use. Recommended reference for smearing temperature: when the room temperature is 20°C, the oil temperature is 80°C; when the room temperature is 25°C, the oil temperature is 45°C; when the room temperature is lower than 17°C or higher than 27°C, the test should not be carried out. Air-conditioned room. A vertical decontamination machine with a freezer should be used if necessary.

2)污片的制备2) Preparation of dirty sheets

将载玻片(110cm×110cm)上沿画出100cm线,以示涂污限制在此线以下;将载玻片下沿画出50cm线,以示擦拭多余油污限制在此线以下。Draw a 100cm line on the upper edge of the glass slide (110cm×110cm) to show that smearing is limited below this line; draw a 50cm line on the bottom edge of the glass slide to show that excess oil wiping is limited below this line.

3)新购载玻片需要在水中煮沸15min后,清水洗涤至不挂水珠再置酸性洗液中浸泡1h后,清水漂洗及蒸馏水冲洗,置干燥箱干燥后备用。3) The newly purchased glass slides need to be boiled in water for 15 minutes, washed with clean water until no water droplets are formed, and then soaked in acid washing solution for 1 hour, rinsed with clean water and distilled water, and dried in a drying box for later use.

4)涂污4) Smudge

将洁净的载玻片以四片为一组置称量架上,用分析天平精确称重(准确至1mg)为m0,将称重后的载玻片逐一夹于晾片架上,夹子应夹在载玻片上沿线以上,将晾片架置搪盘内准备涂污。Place the clean glass slides in groups of four on the weighing rack, accurately weigh them with an analytical balance (accurate to 1 mg) as m 0 , and clamp the weighed glass slides on the drying rack one by one. It should be clamped on the glass slide above the line, and the drying slide should be placed in the lining plate to prepare for smearing.

待油污保持在确定的温度时,逐一将载玻片连同夹子从晾片架上取下,手持夹子将载玻片浸入油污中至100cm上沿线以下(1-2)s,缓缓取出,待油污下滴速度变慢后,挂回原来晾片架上依次制备污片。油污凝固后,将污片取下用滤纸或脱脂棉将污片下沿50cm内底边及两侧多余的油污擦掉,再用镊子夹沾有石油醚的脱脂棉擦拭干净。室温下晾置4h后,在称量架上用分析天平精确称量为m1。此时每组污片上污量应保证(5±0.5)g。When the oil stain is kept at a certain temperature, remove the slides and the clips from the drying rack one by one, immerse the glass slides in the oil stain to 100cm below the upper line (1-2) s with the clips, and take them out slowly. After the dripping speed of the oil stains becomes slow, hang them back on the original drying rack to prepare the stained sheets in turn. After the oil stains solidify, remove the stained sheet and wipe off the excess oil stains along the 50cm inner bottom edge and both sides of the stained sheet with filter paper or absorbent cotton, and then use tweezers to clean the absorbent cotton with petroleum ether. After standing at room temperature for 4 hours, accurately weighed to m 1 with an analytical balance on a weighing rack. At this time, the amount of dirt on each group of dirt sheets should be guaranteed to be (5±0.5) g.

5)试验程序5) Test procedure

采用相同量的实施例1-10和市售洗涤剂对已知涂污量的载玻片进行洗涤,沿着载玻片一个方向,单方向的对载玻片进行擦拭,擦拭10次后,将载玻片放置在清水中,静置5分钟后取出,烘干,称量为m2Use the same amount of Examples 1-10 and commercially available detergents to wash the slides with known smeared amount, wipe the slides in one direction along the slides, after wiping 10 times, The slides were placed in clean water, left standing for 5 minutes, taken out, dried, and weighed as m 2 .

6)结果表示:去油率ω=(m1-m2)/(m1-m0)×100%。6) The results are expressed as follows: oil removal rate ω=(m 1 −m 2 )/(m 1 −m 0 )×100%.

式中:m0-涂污前载玻片质量,g;m1-涂污后载玻片质量,g;m2-洗涤后污片的质量,g。In the formula: m 0 - the mass of the slide before smearing, g; m 1 - the mass of the slide after smearing, g; m 2 - the mass of the stained slide after washing, g.

表1去油率测试表Table 1 Oil removal rate test table

Figure BDA0001753568580000141
Figure BDA0001753568580000141

Figure BDA0001753568580000151
Figure BDA0001753568580000151

本发明中,所述市售洗涤剂为购买自超市的白猫柠檬红茶洗洁精。In the present invention, the commercially available detergent is a white cat lemon black tea detergent purchased from a supermarket.

测试2:污渍重沉淀测试:Test 2: Stain Heavy Settling Test:

将测试1中经过洗涤后的进行重新的污片制备操作,计算上污率以及再次去油率。After washing in Test 1, the soiling sheet preparation operation was performed again, and the soiling rate and the oil-removing rate were calculated.

重新的污片制备操作:Re-fouling flake preparation operation:

将洁净的载玻片以四片为一组置称量架上,用分析天平精确称重(准确至1mg)为m0’,将称重后的载玻片逐一夹于晾片架上,夹子应夹在载玻片上沿线以上,将晾片架置搪盘内准备涂污。Place the clean glass slides in groups of four on the weighing rack, accurately weigh them with an analytical balance (accurate to 1 mg) as m 0 ', and clamp the weighed glass slides on the drying rack one by one. The clip should be clamped above the line on the glass slide, and the drying slide should be placed in the lining tray to prepare for smearing.

待油污保持在确定的温度时,逐一将载玻片连同夹子从晾片架上取下,手持夹子将载玻片浸入油污中至100cm上沿线以下(1-2)s,缓缓取出,待油污下滴速度变慢后,挂回原来晾片架上依次制备污片。油污凝固后,将污片取下用滤纸或脱脂棉将污片下沿50cm内底边及两侧多余的油污擦掉,再用镊子夹沾有石油醚的脱脂棉擦拭干净。室温下晾置4h后,在称量架上用分析天平精确称量为m1’。此时不必保证每组污片上污量为(5±0.5)g。When the oil stain is kept at a certain temperature, remove the slides and the clips from the drying rack one by one, immerse the glass slides in the oil stain to 100cm below the upper line (1-2) s with the clips, and take them out slowly. After the dripping speed of the oil stains becomes slow, hang them back on the original drying rack to prepare the stained sheets in turn. After the oil stains solidify, remove the stained sheet and wipe off the excess oil stains along the 50cm inner bottom edge and both sides of the stained sheet with filter paper or absorbent cotton, and then use tweezers to clean the absorbent cotton with petroleum ether. After standing at room temperature for 4 hours, it was accurately weighed as m 1 ' on a weighing rack with an analytical balance. At this time, it is not necessary to ensure that the amount of dirt on each group of dirt sheets is (5±0.5) g.

上污率=(m1’-m0’)/(m1-m0)×100%。Staining rate=(m 1 '-m 0 ')/(m 1 -m 0 )×100%.

同时将重新制备的污片进行测试1中试验程序的操作,得到质量为m2’。At the same time, the re-prepared soil sheet was subjected to the operation of the test procedure in Test 1 to obtain a mass of m 2 '.

再次去油率:ω’=(m1’-m2’)/(m1’-m0’)×100%。Re-oil removal rate: ω'=(m 1 '-m 2 ')/(m 1 '-m 0 ')×100%.

表2重新去油率测试表Table 2 Re-oil removal rate test table

Figure BDA0001753568580000152
Figure BDA0001753568580000152

Figure BDA0001753568580000161
Figure BDA0001753568580000161

测试3:去污力性能测试,大体参照标准GB 9985的要求进行去污力的性能测试。Test 3: Detergency performance test, generally refer to the requirements of the standard GB 9985 to conduct the detergency performance test.

表3去污力性能测试Table 3 Detergency performance test

实施例Example 去污力,%Detergency, % 实施例1Example 1 91.391.3 实施例2Example 2 81.581.5 实施例3Example 3 75.275.2 实施例4Example 4 73.573.5 实施例5Example 5 52.052.0 实施例6Example 6 61.161.1 实施例7Example 7 72.172.1 实施例8Example 8 45.545.5 实施例9Example 9 62.962.9 实施例10Example 10 68.768.7 市售洗涤剂Commercial detergent 30.130.1

以上所述仅为本发明的较佳实施例,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。The above are only preferred embodiments of the present invention and are not intended to limit the present invention. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principles of the present invention shall be included in the protection of the present invention. within the range.

Claims (2)

1. The super-strong cleaning nano coral calcium powder cleaning agent is characterized by comprising the following preparation raw materials:
the component A comprises: surfactant, nano coral calcium powder, sodium citrate and chelating agent; the nano coral calcium powder is polysaccharide modified coral calcium powder, and the polysaccharide is pectin; the chelating agent is one or two of ethylene diamine tetraacetic acid tetrasodium, sodium tartrate, hydroxyethylidene diphosphonic acid tetrasodium and imino disuccinic acid tetrasodium; the surfactant is a nonionic surfactant and an anionic surfactant in a weight ratio of 1: 2; the non-ionic surfactant is selected from one or more of tween-20, tween-60 and tween-80; the anionic surfactant is sodium dodecyl benzene sulfonate;
and B component: radix Stemonae extract, cortex Phellodendri extract, Raphani semen extract, and herba Artemisiae Scopariae extract;
and C, component C: tannins;
the preparation method of the polysaccharide modified nano coral calcium powder comprises the following steps:
1. dripping a small amount of deionized water into the nano coral calcium powder at room temperature, and uniformly dispersing the nano coral calcium powder after ultrasonic oscillation treatment;
2. dispersing polysaccharide in water solution to prepare polysaccharide solution with the concentration of 3%;
3. gradually dropping a polysaccharide solution into the nano coral calcium powder slurry obtained in the step 1 under an ultrasonic condition, continuing ultrasonic treatment for 10 minutes after the dropping is finished, freezing the mixed solution at-80 ℃ for 12 hours, and freeze-drying to obtain polysaccharide modified nano coral calcium powder;
wherein the weight ratio of the polysaccharide to the nano coral calcium powder is 1: 2;
the component B is coated by a slow release film;
the slow release film is modified rhamnose;
the preparation method of the component B comprises the following steps:
s01, dissolving 1.5g of rhamnose in 100mL of 2% acetic acid aqueous solution, and stirring and dissolving by using a magnetic stirrer; 1g of polyvinyl alcohol is dissolved in 30mL of water and heated to be dissolved; uniformly stirring and mixing the rhamnose and the polyvinyl alcohol solution, carrying out water bath at 50 ℃ for 48h, adding 1.6-2.8g of 200-mesh 300-mesh silica gel into 40mL of the mixed solution, pouring into a glass plate, and evaporating at room temperature to form a film; immersing the obtained dried membrane into 2mol/L sodium hydroxide solution, and dissolving silica gel in water bath at 50 ℃ for 2h to obtain rhamnose/polyvinyl alcohol; neutralizing redundant sodium hydroxide by using 5% acetic acid, washing the solution to be neutral by using deionized water, and drying the solution in a drying box;
s02 mixing radix Stemonae extract, cortex Phellodendri extract, Raphani semen extract, and herba Artemisiae Scopariae extract to obtain extract mixture;
s03, mixing 10g of rhamnose/polyvinyl alcohol prepared in the step 1 and 80g of distilled water, adding 6g of the extract mixture at room temperature, uniformly stirring, performing ultrasonic treatment for 30min to uniformly mix, and performing spray drying at the conditions of an inlet temperature of 175 ℃, a feed flow rate of 3mL/min, a nozzle head diameter of 0.7mm and nozzle cleaning for 2 times/min to obtain a component B;
the extraction method of the stemona extract and the phellodendron extract comprises the following steps:
(1) selecting 1 part of radix stemonae and 1 part of phellodendron bark, cleaning, drying, grinding, adding 10 parts of lime milk, uniformly stirring, putting into a percolating cylinder, soaking for 6 hours by using lime water, taking a percolate, adding 120% of the volume of the percolate, adding a citric acid saturated aqueous solution, stirring, standing overnight, filtering and taking a precipitate;
(2) dissolving the precipitate with hot water, filtering, and collecting filtrate to obtain radix Stemonae extract and cortex Phellodendri extract crude product;
(3) dissolving the crude product in boiling water, and filtering to obtain radix Stemonae extract and cortex Phellodendri extract;
the weight ratio of the component A to the component B to the component C is 8: 4: 1;
in the component A, the weight ratio of the surfactant, the nano coral calcium powder, the sodium citrate and the chelating agent is 1: 1: 0.5: 0.01;
in the component B, the weight ratio of the stemona root extract to the phellodendron bark extract to the radish seed extract to the oriental wormwood extract is 1: 1: 1: 1.
2. the super-cleaning nano coral calcium powder cleaning agent as claimed in claim 1, wherein the tannin is a hydrolyzed tannin.
CN201810877156.6A 2018-08-03 2018-08-03 A kind of super cleaning power nano coral calcium powder cleaning agent and preparation method thereof Active CN108728269B (en)

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