CN113616838A

CN113616838A - Sterilization deodorant

Info

Publication number: CN113616838A
Application number: CN202111016781.XA
Authority: CN
Inventors: 张建洪
Original assignee: Shanghai Changfan Biotechnology Co ltd
Current assignee: Shanghai Changfan Biotechnology Co ltd
Priority date: 2021-08-31
Filing date: 2021-08-31
Publication date: 2021-11-09

Abstract

The invention discloses a sterilization deodorant, which consists of the following substances in percentage by weight: 0.7-1.2% of soyabean ethyl sulfate morpholine, 4-8% of dealdehydized alcohol, 0.5-1.5% of beta-cyclodextrin, 0.3-0.7% of silver ion bactericide, 1-3% of shaddock peel, 0.5-1.2% of essence, 1-3% of hawthorn seed particles, 1.5-2.5% of traditional Chinese medicine extract, 1.2-1.8% of stabilizer and 89.1-90% of DI WATER. According to the invention, the added soybean ethyl sulfate morpholine eliminates odor through a bonding effect, and meanwhile, the shaddock peel and essence are heated, so that the odor removing function can be further increased, the odor can be rapidly removed, meanwhile, the added silver ion bactericide and hawthorn kernel particles can be used for efficiently performing sterilization treatment, can be long-acting antibacterial, are nontoxic, tasteless, non-irritant and non-allergic, cannot cause drug resistance of bacteria, and in addition, the traditional Chinese medicine extract is added, so that the protection effect on a human body can be increased.

Description

Sterilization deodorant

Technical Field

The invention belongs to the technical field of sterilization deodorant, and particularly relates to a sterilization deodorant.

Background

The sterilization deodorant has no toxic or side effect on human bodies and livestock, is safe to use, has antibacterial, sterilization and deodorization effects, and has good decomposition and removal effects on ammonia, hydrogen sulfide and other malodors.

The existing sterilization deodorant also has some problems: the traditional sterilization deodorant has the advantages that the bad smell is covered by the essence, the bad smell cannot be eliminated, the deodorization effect is poor, meanwhile, during sterilization, bacteria easily generate drug resistance, and long-acting antibiosis is not facilitated, so that the sterilization effect is reduced, and therefore, the sterilization deodorant is provided.

Disclosure of Invention

The invention aims to provide a sterilization deodorant, which solves the problems in the background technology.

In order to achieve the purpose, the invention provides the following technical scheme: a sterilization deodorant consists of the following substances in percentage by weight: 0.7-1.2% of soyabean ethyl sulfate morpholine, 4-8% of dealdehydized alcohol, 0.5-1.5% of beta-cyclodextrin, 0.3-0.7% of silver ion bactericide, 1-3% of shaddock peel, 0.5-1.2% of essence, 1-3% of hawthorn seed particles, 1.5-2.5% of traditional Chinese medicine extract, 1.2-1.8% of stabilizer and 89.1-90% of DI WATER.

Preferably, the composition comprises the following substances in percentage by weight: 0.8-1.1% of soyabean ethyl sulfate morpholine, 4.5-7.8% of dealdehydized alcohol, 0.6-1.2% of beta-cyclodextrin, 0.3-0.6% of silver ion bactericide, 1.2-2.8% of shaddock peel, 0.6-1.0% of essence, 1.2-2.8% of hawthorn seed particles, 1.8-2.8% of traditional Chinese medicine extract, 1.4-1.6% of stabilizer and 89.1-89.7% of DI WATER.

Preferably, the composition comprises the following substances in percentage by weight: 0.9-1.1% of soyabean ethyl sulfate morpholine, 9.2-9.6% of dealdehydized alcohol, 0.6-1.2% of beta-cyclodextrin, 0.4-0.6% of silver ion bactericide, 1.2-2.8% of shaddock peel, 0.6-1.0% of essence, 1.2-2.8% of hawthorn seed particles, 1.8-2.8% of traditional Chinese medicine extract, 1.4-1.6% of stabilizer and 89.1-89.5% of DI WATER.

Preferably, the composition comprises the following substances in percentage by weight: 1% of soybean ethyl sulfate morpholine, 9.3% of dealdehydized alcohol, 0.8% of beta-cyclodextrin, 0.5% of silver ion bactericide, 1.6% of shaddock peel, 0.8% of essence, 1.8% of hawthorn seed granules, 2% of traditional Chinese medicine extract, 1.5% of stabilizer and 89.2% of DI WATER.

Preferably, the stabilizer is selected from at least one of diisocyanate, maleic anhydride, boric acid, borax, glutaraldehyde, and persulfate.

Preferably, the preparation process of the sterilizing deodorant comprises the following steps: adding DI WATER into a material preparing pot, adding the soybean ethyl sulfate morpholine, beta-cyclodextrin, shaddock peel, essence, hawthorn seed particles and the traditional Chinese medicine extract into the DI WATER, stirring uniformly, then adding dealdehydized alcohol, stirring uniformly, finally adding the silver ion bactericide and the stabilizer, stopping stirring after stirring uniformly, sampling to be detected, and filling after the inspection is qualified.

Preferably, the stirring speed is 500-1500r/min, and the time of each stirring is 2-4 h.

Preferably, the test process comprises sterilization detection and deodorization detection, wherein the sterilization detection comprises detection of the content of escherichia coli, staphylococcus aureus and candida albicans, and the deodorization detection comprises detection of the content of ammonia and hydrogen sulfide.

Compared with the prior art, the invention has the beneficial effects that: according to the invention, the added soybean ethyl sulfate morpholine eliminates odor through a bonding effect, and meanwhile, the shaddock peel and essence are heated, so that the odor removing function can be further increased, the odor can be rapidly removed, meanwhile, the added silver ion bactericide and hawthorn kernel particles can be used for efficiently performing sterilization treatment, can be long-acting antibacterial, are nontoxic, tasteless, non-irritant and non-allergic, cannot cause drug resistance of bacteria, and in addition, the traditional Chinese medicine extract is added, so that the protection effect on a human body can be increased.

Drawings

FIG. 1 is a process flow diagram of the present invention.

Detailed Description

The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

Example 1

The invention provides a technical scheme that: a sterilization deodorant consists of the following substances in percentage by weight: 0.7% of soyabean ethyl sulfate morpholine, 4% of dealdehydized alcohol, 0.5% of beta-cyclodextrin, 0.3% of silver ion bactericide, 1% of shaddock peel, 0.5% of essence, 1% of hawthorn seed particles, 1.5% of traditional Chinese medicine extract, 1.2% of stabilizer and 89.1% of DI WATER.

In this embodiment, preferably, the stabilizer is selected from diisocyanates.

In this embodiment, preferably, the production process of the dealdehydized alcohol is as follows: the method comprises the following steps:

s11, raw material acceptance: selecting grains with starch content of 30 as raw materials, and cleaning with clear water for later use;

s12, impurity removal of raw materials: conveying the cleaned raw materials to a stone remover and an impurity remover through a belt conveyor to remove silt, stones and metal impurities in the raw material grains;

s13, raw material crushing: weighing the raw materials after removing impurities, conveying the raw materials to a hammer mill through a belt conveyor for crushing to obtain raw material powder, wherein in the raw material crushing process, the mesh diameter of a screen mesh used by the hammer mill is 0.8mm, and the crushed raw material powder is 15 meshes;

s14, stirring raw material powder: pouring the crushed raw material powder into a stirring tank, adding process water, distilled residual water, CaCl2 and high-temperature-resistant alpha-amylase into the stirring tank, and uniformly stirring; the ratio of the raw material powder, the process water, the distilled residual water, the CaCl2 and the high-temperature-resistant alpha-amylase is 2:7:0.5:0.25: 0.25;

s15, precooking and puffing: feeding the stirred material obtained in the step S14 into a liquefaction tank, heating to 95 ℃ under the pressure of 150Pa, and liquefying for 2 hours to obtain liquefied mash;

s16, saccharification: sending the liquefied mash to a saccharification tank, adding 50% of vinasse centrifugal liquid into the liquefied mash to reduce the pH value of the liquefied mash to 4.5, cooling to 60 ℃ by a spiral plate heat exchanger, adding saccharifying enzyme into the saccharification tank, immediately cooling to 30 ℃ by the spiral plate heat exchanger to obtain the saccharified mash, wherein the DE value of the saccharified mash is 2%;

s17, fermentation: cooling the saccharified mash to a fermentation temperature of 29 ℃ by a spray cooler, inoculating dry yeast with the saccharified mash amount of 9% by taking immobilized yeast as a carrier, uniformly mixing, fermenting for 55h, and adding carbendazim to sterilize the fermented mash in the fermentation process so as to prevent the growth of microorganisms;

s18, distillation: feeding the fermented mash into a distillation tower with a set temperature of 75 ℃, simultaneously adding 9% by mass of sodium hydroxide, distilling for 18min, purifying alcohol in the mash, circularly distilling the alcohol which does not reach the concentration index, and discharging vinasse and alcohol wastewater from a vinasse groove;

s19, cooling: and cooling the alcohol extracted from the distillation tower to normal temperature by a plate cooler to obtain the dealdehydized alcohol.

In this embodiment, preferably, the raw potatoes selected in S11 are cassava, sweet potatoes, potatoes and yams, the water content of the raw materials is 8%, the metal removed in the impurity removal process of the raw materials in S12 is iron, and the used impurity remover removes iron electromagnetically.

In this embodiment, preferably, after the alcohol wastewater in S18 is discharged, the wastewater needs to be treated by the following steps: step one, removing larger impurities from the alcohol wastewater through a grid, and then, allowing the alcohol wastewater to enter an adjusting tank to effectively adjust the water quantity and the water quality; step two, lifting the mixture into a primary sedimentation tank by using a pump for pretreatment, adding an alcohol wastewater treatment agent into the primary sedimentation tank at the stage, uniformly mixing the alcohol wastewater treatment agent and the alcohol wastewater treatment agent, and standing for 35 min; and step three, the wastewater treated in the step three enters a hydrolysis acidification tank and a contact oxidation tank for biochemical treatment, the effluent enters a secondary sedimentation tank for mud-water separation, one part of sludge in the secondary sedimentation tank flows back to the front of an aerobic tank, and the other part of sludge is discharged to a sludge tank.

In this embodiment, preferably, the production process of the silver ion bactericide mainly includes the steps of: taking raw material silver and fruit acid, processing the raw material silver into analytically pure silver, then adding the fruit acid, heating and stirring, then filtering the silver ion solution, detecting, and packaging the stock solution finished product to obtain the silver ion bactericide.

In this embodiment, preferably, the DI WATER is prepared by using reverse osmosis-ion exchange equipment, and the basic process flow is as follows: raw water, a multi-media filter, an activated carbon filter, a precision filter, reverse osmosis equipment, a mixed bed, an ultra-pure water tank, an ultra-pure water pump, a post cartridge filter and deionized water.

In this embodiment, preferably, the preparation process of the sterilizing deodorant is as follows: adding DI WATER into a material preparing pot, adding the soybean ethyl sulfate morpholine, beta-cyclodextrin, shaddock peel, essence, hawthorn seed particles and the traditional Chinese medicine extract into the DI WATER, stirring uniformly, then adding dealdehydized alcohol, stirring uniformly, finally adding the silver ion bactericide and the stabilizer, stopping stirring after stirring uniformly, sampling to be detected, and filling after the inspection is qualified.

In this embodiment, the stirring speed is preferably 500r/min, and the time for each stirring is preferably 4 h.

Example 2

The invention provides a technical scheme that: a sterilization deodorant consists of the following substances in percentage by weight: 1.2% of soyabean ethyl sulfate morpholine, 8% of dealdehydized alcohol, 1.5% of beta-cyclodextrin, 0.7% of silver ion bactericide, 3% of shaddock peel, 1.2% of essence, 3% of hawthorn seed particles, 2.5% of traditional Chinese medicine extract, 1.8% of stabilizer and 90% of DI WATER.

s11, raw material acceptance: selecting grains with starch content of 40% as raw materials, and cleaning with clear water for later use;

s13, raw material crushing: weighing the raw materials after removing impurities, conveying the raw materials to a hammer mill through a belt conveyor for crushing to obtain raw material powder, wherein in the raw material crushing process, the mesh diameter of a screen mesh used by the hammer mill is 1.6mm, and the crushed raw material powder is 45 meshes;

s16, saccharification: sending the liquefied mash to a saccharification tank, adding 50% of vinasse centrifugal liquid into the liquefied mash to reduce the pH value of the liquefied mash to 4.5, cooling to 60 ℃ by a spiral plate heat exchanger, adding saccharifying enzyme into the saccharification tank, immediately cooling to 30 ℃ by the spiral plate heat exchanger to obtain the saccharified mash, wherein the DE value of the saccharified mash is 3%;

s17, fermentation: cooling the saccharified mash to a fermentation temperature of 34 ℃ by a spray cooler, inoculating dry yeast with 16% of the saccharified mash by taking immobilized yeast as a carrier, uniformly mixing, fermenting for 85h, and adding carbendazim to sterilize the fermented mash in the fermentation process so as to prevent the growth of microorganisms;

s18, distillation: feeding the fermented mash into a distillation tower with a set temperature of 90 ℃, simultaneously adding 21% by mass of sodium hydroxide, distilling for 32min, purifying alcohol in the mash, circularly distilling the alcohol which does not reach the concentration index, and discharging vinasse and alcohol wastewater from a vinasse groove;

In this embodiment, preferably, the raw potatoes selected in S11 are cassava, sweet potatoes, potatoes and yams, the water content of the raw materials is 15%, the metal removed in the impurity removal process of the raw materials in S12 is iron, and the used impurity remover removes iron electromagnetically.

In this embodiment, preferably, after the alcohol wastewater in S18 is discharged, the wastewater needs to be treated by the following steps: step one, removing larger impurities from the alcohol wastewater through a grid, and then, allowing the alcohol wastewater to enter an adjusting tank to effectively adjust the water quantity and the water quality; step two, lifting the mixture into a primary sedimentation tank by using a pump for pretreatment, adding an alcohol wastewater treatment agent into the primary sedimentation tank at the stage, uniformly mixing the alcohol wastewater treatment agent and the alcohol wastewater treatment agent, and standing for 45 min; and step three, the wastewater treated in the step three enters a hydrolysis acidification tank and a contact oxidation tank for biochemical treatment, the effluent enters a secondary sedimentation tank for mud-water separation, one part of sludge in the secondary sedimentation tank flows back to the front of an aerobic tank, and the other part of sludge is discharged to a sludge tank.

In this embodiment, preferably, the DI WATER is prepared by matching reverse osmosis equipment and electrodeionization equipment, and the basic process flow is as follows: raw water, a multi-medium filter, an activated carbon filter, a precision filter, a reverse osmosis device, electric deionization, an ultra-pure water tank, an ultra-pure water pump, a post cartridge filter and deionized water.

In this embodiment, the stirring speed is 1500r/min, and the time for each stirring is preferably 2 h.

Example 3

The invention provides a technical scheme that: a sterilization deodorant consists of the following substances in percentage by weight: 1% of soybean ethyl sulfate morpholine, 9.3% of dealdehydized alcohol, 0.8% of beta-cyclodextrin, 0.5% of silver ion bactericide, 1.6% of shaddock peel, 0.8% of essence, 1.8% of hawthorn seed granules, 2% of traditional Chinese medicine extract, 1.5% of stabilizer and 89.2% of DI WATER.

The invention has the advantages that: according to the invention, the added soybean ethyl sulfate morpholine eliminates odor through a bonding effect, and meanwhile, the shaddock peel and essence are heated, so that the odor removing function can be further increased, the odor can be rapidly removed, meanwhile, the added silver ion bactericide and hawthorn kernel particles can be used for efficiently performing sterilization treatment, can be long-acting antibacterial, are nontoxic, tasteless, non-irritant and non-allergic, cannot cause drug resistance of bacteria, and in addition, the traditional Chinese medicine extract is added, so that the protection effect on a human body can be increased.

Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims

1. A sterilization deodorant is characterized in that: the composition comprises the following substances in percentage by weight: 0.7-1.2% of soyabean ethyl sulfate morpholine, 4-8% of dealdehydized alcohol, 0.5-1.5% of beta-cyclodextrin, 0.3-0.7% of silver ion bactericide, 1-3% of shaddock peel, 0.5-1.2% of essence, 1-3% of hawthorn seed particles, 1.5-2.5% of traditional Chinese medicine extract, 1.2-1.8% of stabilizer and 89.1-90% of DIWATER.

2. A bactericidal deodorant as set forth in claim 1, wherein: the composition comprises the following substances in percentage by weight: 0.8-1.1% of soyabean ethyl sulfate morpholine, 4.5-7.8% of dealdehydized alcohol, 0.6-1.2% of beta-cyclodextrin, 0.3-0.6% of silver ion bactericide, 1.2-2.8% of shaddock peel, 0.6-1.0% of essence, 1.2-2.8% of hawthorn seed particles, 1.8-2.8% of traditional Chinese medicine extract, 1.4-1.6% of stabilizer and 89.1-89.7% of DIWATER.

3. A bactericidal deodorant as set forth in claim 2, wherein: the composition comprises the following substances in percentage by weight: 0.9-1.1% of soyabean ethyl sulfate morpholine, 9.2-9.6% of dealdehydized alcohol, 0.6-1.2% of beta-cyclodextrin, 0.4-0.6% of silver ion bactericide, 1.2-2.8% of shaddock peel, 0.6-1.0% of essence, 1.2-2.8% of hawthorn seed particles, 1.8-2.8% of traditional Chinese medicine extract, 1.4-1.6% of stabilizer and 89.1-89.5% of DIWATER.

4. A bactericidal deodorant as set forth in claim 3, wherein: the composition comprises the following substances in percentage by weight: 1% of soyabean ethyl sulfate morpholine, 9.3% of dealdehydized alcohol, 0.8% of beta-cyclodextrin, 0.5% of silver ion bactericide, 1.6% of shaddock peel, 0.8% of essence, 1.8% of hawthorn seed granules, 2% of traditional Chinese medicine extract, 1.5% of stabilizer and 89.2% of DIWATER.

5. A bactericidal deodorant as set forth in claim 1, wherein: the stabilizer is at least one selected from diisocyanate, maleic anhydride, boric acid, borax, glutaraldehyde and persulfate.

6. The sterilizing deodorant according to claim 1, wherein the sterilizing deodorant is prepared by the following process: adding DIWATER into a material preparing pot, adding the soyabean ethyl sulfate morpholine, beta-cyclodextrin, shaddock peel, essence, hawthorn seed particles and the traditional Chinese medicine extract into the DIWATER, uniformly stirring, then adding dealdehydized alcohol, uniformly stirring, finally adding the silver ion bactericide and the stabilizer, stopping stirring after uniformly stirring, sampling to be detected, and filling after the inspection is qualified.

7. The bactericidal deodorant as set forth in claim 5, wherein: the stirring speed is 500-1500r/min, and the stirring time is 2-4 h.

8. The bactericidal deodorant as set forth in claim 6, wherein: the detection process comprises sterilization detection and deodorization detection, wherein the sterilization detection comprises the detection of the content of escherichia coli, staphylococcus aureus and candida albicans, and the deodorization detection comprises the detection of the content of ammonia and hydrogen sulfide.