CN109287499B - Cat litter with pet urine protein early warning function and preparation method thereof - Google Patents

Cat litter with pet urine protein early warning function and preparation method thereof Download PDF

Info

Publication number
CN109287499B
CN109287499B CN201811247499.0A CN201811247499A CN109287499B CN 109287499 B CN109287499 B CN 109287499B CN 201811247499 A CN201811247499 A CN 201811247499A CN 109287499 B CN109287499 B CN 109287499B
Authority
CN
China
Prior art keywords
silica gel
cat litter
solution
urine protein
soaking
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201811247499.0A
Other languages
Chinese (zh)
Other versions
CN109287499A (en
Inventor
宋兴良
胡雪萍
高振珅
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Maidu Chongyi Shanghai Technology Development Co ltd
Original Assignee
Linyi University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Linyi University filed Critical Linyi University
Priority to CN201811247499.0A priority Critical patent/CN109287499B/en
Publication of CN109287499A publication Critical patent/CN109287499A/en
Application granted granted Critical
Publication of CN109287499B publication Critical patent/CN109287499B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01KANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K1/00Housing animals; Equipment therefor
    • A01K1/015Floor coverings, e.g. bedding-down sheets ; Stable floors
    • A01K1/0152Litter
    • A01K1/0155Litter comprising organic material
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01KANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K1/00Housing animals; Equipment therefor
    • A01K1/015Floor coverings, e.g. bedding-down sheets ; Stable floors
    • A01K1/0152Litter
    • A01K1/0154Litter comprising inorganic material

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Environmental Sciences (AREA)
  • Zoology (AREA)
  • Animal Husbandry (AREA)
  • Biodiversity & Conservation Biology (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Housing For Livestock And Birds (AREA)

Abstract

The invention discloses cat litter with a pet urine protein early warning function and a preparation method thereof. The cat litter is prepared from the following raw materials: modified fine-pore silica gel, diatomite, activated carbon, a urine protein indicator and an antibacterial agent. According to the invention, the biuret reaction is applied to the preparation process of the cat litter, and the dosage of the silica gel substrate material and the urine protein indicator is scientifically matched, so that the color reaction can be generated on abnormal urine of urine protein, and the color reaction does not exist on normal urine, therefore, the health condition of pets can be preliminarily reflected, and the pet with abnormal urine can be diagnosed and examined in time, so that an early warning effect is achieved. The invention also modifies silica gel, effectively increases the hydrophilicity, enhances the dip dyeing effect of the silica gel and the urine protein indicator, and ensures that the color reaction is obviously and easily distinguished. Meanwhile, the novel antibacterial agent is added, so that the cat litter has an obvious antibacterial effect and good persistence, and does not need to be replaced frequently. The invention has simple preparation process and low cost, and is suitable for popularization and use.

Description

Cat litter with pet urine protein early warning function and preparation method thereof
Technical Field
The invention belongs to the technical field of cat litter preparation, and particularly relates to a silica gel cat litter with a cat urine protein early warning function and a preparation method thereof.
Background
The cat litter is a pet product with large consumption, the number of domestic pets such as cats and dogs is increasing along with the social development and the improvement of the living standard of people, the sanitary treatment of excrement and urine becomes an important problem for environmental protection, and the cat litter becomes a common necessary product for most families breeding the pets.
The cat litter commonly used in the market at present comprises bentonite, clay, paper scraps, wood powder, silica gel cat litter and the like, but the cat litter is not convenient for users to clean because the deodorization capability of the bentonite clay cat litter is not ideal, mildew and much dust are easily generated after the cat litter is wetted, the condensation force of the paper scraps cat litter is weak, the cat litter is easy to become paste after moisture absorption, and the like. The wood flour cat litter is more environment-friendly, but the number of manufacturers is less at present.
The silica gel cat litter is characterized in that the silica gel cat litter is used as pet padding. The silica gel cat litter is a latest and most ideal pet litter detergent, the main component of the detergent is silicon dioxide, the content of the silica gel cat litter is up to more than 98%, the silica gel cat litter is white granular in appearance, the safety degree of household use is high, and the silica gel cat litter is a cat litter product which is popular with consumers in the international market at present. The existing silica gel cat litter has the main functions of adsorption deodorization, single function and high manufacturing cost. It is necessary to develop a cat litter product which has low cost and simple preparation process, can efficiently adsorb and deodorize and can reflect abnormal health of pets.
Disclosure of Invention
In order to solve the problems of high manufacturing cost, poor performance and single function of the existing cat litter product, the invention provides the cat litter with the pet urine protein early warning function and the preparation method thereof, and the cat litter takes the fine-pore silica gel as a base material and carries out hydrophilic modification on the fine-pore silica gel to enhance the dip-dyeing effect of the protein indicator; diatomite activated carbon is added to enhance the adsorption and deodorization capacity of the silica gel cat litter; and a novel double-arc antibacterial agent is added to realize a high-efficiency antibacterial and bacteriostatic function. In order to realize the purpose of the invention, the adopted technical scheme is as follows:
the cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 60-100 parts of modified fine-pore silica gel, 5-10 parts of diatomite, 5-10 parts of activated carbon, 100-150 parts of urine protein indicator and 0.1-0.5 part of antibacterial agent; the urine protein indicator is a bromophenol blue reagent or a biuret reagent.
The bromophenol blue reagent is prepared by the following method: 0.67g of bromophenol blue is dissolved in 10ml of 0.1mol/L NaOH solution and distilled water is added to 1000 ml.
The biuret reagent is prepared by the following method: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
the modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: 0.2mol/L citric acid solution 1000m1 is added toL Na2HPO4Adjusting the pH value of the solution to be 2.1 by 20ml to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: preparing a biuret reagent, weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving with 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution under stirring, and diluting with water to 1L; preparing a bromophenol blue reagent, namely weighing 0.67g of bromophenol blue, dissolving the bromophenol blue in 10ml of 0.1mol/L NaOH solution, and adding distilled water to 1000 ml;
(4) weighing modified pore silica gel and biuret urine protein indicator according to a ratio, soaking the modified pore silica gel in biuret urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing the silica gel particles in a vacuum drying oven for vacuum drying to obtain a primary finished product A1; weighing modified porous silica gel and bromophenol blue urine protein indicator according to a ratio, soaking the modified porous silica gel in bromophenol blue urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing in a vacuum drying oven for vacuum drying to obtain a primary finished product A2;
(5) mixing the diatomite, the activated carbon and the primary finished product A1 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B1;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; placing the mixed particles B1 obtained in the step (5) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C1;
(7) mixing the diatomite, the activated carbon and the primary finished product A2 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B2;
(8) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; and (3) placing the mixed particles B2 obtained in the step (A) in a rotating disc, uniformly spraying an antibacterial agent solution on the mixed particles B2, placing the particles in a vacuum drying oven to be dried after the spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C2.
The mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C1 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C1, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; manufacturing a color comparison card according to the corresponding RGB value;
(2) photographing the finished cat litter C2 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C2, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; and manufacturing a color comparison card according to the corresponding RGB value.
The method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real object Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition, and if so, showing that the RGB value of the photo of the shot cat litter is not different.
During practical application, the color change of the silica gel after the pet excretes and uses is compared with a colorimetric card, whether the urine protein content in the urine of the pet is normal or not is judged quickly, the biuret reagent is used as a urea protein indicator, and when the urine protein exceeds the standard, the silica gel can be changed into purple from blue. When the urine protein exceeds the standard, the silica gel changes from yellow to blue by taking bromophenol blue reagent as a urea protein indicator.
The histopathological manifestations of urinary protein formation are mainly glomerular dilatation, capillary cell injury, and further plasma protein leakage from glomeruli, and renal ischemia causes the renal tubule reabsorption function to weaken, and when the urinary protein filtering amount exceeds the reabsorption amount, the urinary protein formation is caused. Therefore, urine protein generally reflects the degree of damage to the kidney function, and has the functions of primarily predicting kidney damage and accurately diagnosing symptoms of kidney damage. Therefore, the health condition of the pet can be reflected by detecting the urine protein content of the pet. Urine protein can be combined with various chemical reagents to generate a color change phenomenon, so that whether pets have diseases or not can be preliminarily judged through the color change phenomenon reaction.
The invention selects biuret and bromophenol blue as urine protein indicators. The biuret reaction is characteristic of peptides and proteins, compounds having two or more peptide bonds react with Cu under alkaline conditions2+The reaction produces a compound with red-purple color, and the color of the solution changes from basket to purple. The protein indicator used in the invention is applied to the cat litter preparation process by utilizing the color reaction, and can predict the health condition of the pet by judging whether the color of the cat litter changes in the using process, thereby playing roles in warning and preventing. At the same time. In order to improve the dip dyeing effect of the protein indicator, the pore silica gel obtained in the market is modified, so that the hydrophilic performance of the pore silica gel is improved, and the protein indicator can be efficiently dip-dyed on silica gel particles.
The cat litter bactericide selects the hexamethylene biguanide hydrochloride as the cat litter bactericide, can effectively sterilize and bacteriostasis, and compared with other solvent type bactericides, the cat litter bactericide is matched with silica gel particles, does not generate strong pungent smell, has good compatibility, low toxicity to pets, can be used for a long time, does not contain heavy metal and organic halogen, and does not cause adverse effect on the environment.
In conclusion, the beneficial effects of the invention are as follows: according to the invention, the biuret reaction is applied to the preparation process of the cat litter, and the silica gel substrate material and the biuret reagent are scientifically proportioned, so that the color reaction can be generated on abnormal urine protein, and the color reaction is not generated on normal urine, therefore, the health condition of pets can be preliminarily reflected, and the pets with abnormal urine can be diagnosed and examined in time, and an early warning effect is achieved. The added diatomite and the added active carbon are strong adsorptive porous substances, can strongly adsorb water and peculiar smell, and purify air. The invention also modifies silica gel, effectively increases the hydrophilicity of the silica gel, enhances the dip dyeing of the silica gel and biuret reagent, and ensures that the color reaction is obviously and easily distinguished. Meanwhile, the novel antibacterial agent is added, so that the cat litter has an obvious antibacterial effect and good persistence, and does not need to be replaced frequently. The invention has simple preparation process and low cost, and is suitable for popularization and use.
Drawings
FIG. 1 is a standard colorimetric card prepared by using biuret reagent as protein indicator according to the present invention.
Detailed Description
The technical solution of the present invention is further described below with reference to specific embodiments, but is not limited thereto.
Example 1
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 60 parts of modified fine-pore silica gel, 5 parts of diatomite, 5 parts of activated carbon, 100 parts of urine protein indicator and 0.1 part of antibacterial agent; the urine protein indicator is a biuret reagent.
The biuret reagent is prepared by the following method: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
the modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000m1 of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
(4) weighing modified pore silica gel and biuret urine protein indicator according to a ratio, soaking the modified pore silica gel in biuret urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing the silica gel particles in a vacuum drying oven for vacuum drying to obtain a primary finished product A1;
(5) mixing the diatomite, the activated carbon and the primary finished product A1 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B1;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; placing the mixed particles B1 obtained in the step (5) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C1;
the mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C1 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C1, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; manufacturing a color comparison card according to the corresponding RGB value;
the method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real world Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition or not, and if so, indicating that the RGB value of the photo of the shot cat litter is not different.
Example 2
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 80 parts of modified fine-pore silica gel, 8 parts of diatomite, 8 parts of activated carbon, 130 parts of urine protein indicator and 0.3 part of antibacterial agent; the urine protein indicator is a biuret reagent.
The biuret reagent is prepared by the following method: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
the modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000m1 of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
(4) weighing modified pore silica gel and biuret urine protein indicator according to a ratio, soaking the modified pore silica gel in biuret urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing the silica gel particles in a vacuum drying oven for vacuum drying to obtain a primary finished product A1;
(5) mixing the diatomite, the activated carbon and the primary finished product A1 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B1;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; placing the mixed particles B1 obtained in the step (5) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C1;
the mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C1 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C1, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; manufacturing a color comparison card according to the corresponding RGB value;
the method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real world Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition or not, and if so, indicating that the RGB value of the photo of the shot cat litter is not different.
Example 3
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 100 parts of modified fine-pore silica gel, 10 parts of diatomite, 10 parts of activated carbon, 150 parts of urine protein indicator and 0.5 part of antibacterial agent; the urine protein indicator is a biuret reagent.
The biuret reagent is prepared by the following method: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
the modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000m1 of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving the copper sulfate and the potassium sodium tartrate in 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution into the solution under stirring, and diluting the solution to 1L by using water;
(4) weighing modified pore silica gel and biuret urine protein indicator according to a ratio, soaking the modified pore silica gel in biuret urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing the silica gel particles in a vacuum drying oven for vacuum drying to obtain a primary finished product A1;
(5) mixing the diatomite, the activated carbon and the primary finished product A1 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B1;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; placing the mixed particles B1 obtained in the step (5) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C1;
the mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C1 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C1, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; manufacturing a color comparison card according to the corresponding RGB value;
the method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real object Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition, and if so, showing that the RGB value of the photo of the shot cat litter is not different.
Example 4
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 60 parts of modified fine-pore silica gel, 5 parts of diatomite, 5 parts of activated carbon, 100 parts of urine protein indicator and 0.1 part of antibacterial agent; the urine protein indicator is a bromophenol blue reagent.
The bromophenol blue reagent is prepared by the following method: 0.67g of bromophenol blue is dissolved in 10ml of 0.1mol/L NaOH solution and distilled water is added to 1000 ml.
The modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000m1 of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: weighing 0.67g of bromophenol blue, dissolving in 10ml of 0.1mol/L NaOH solution, and adding distilled water to 1000 ml;
(4) weighing modified porous silica gel and bromophenol blue urine protein indicator according to a ratio, soaking the modified porous silica gel in bromophenol blue urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing in a vacuum drying oven for vacuum drying to obtain a primary finished product A2;
(5) mixing the diatomite, the activated carbon and the primary finished product A2 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B2;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; and (3) placing the mixed particles B2 obtained in the step (A) in a rotating disc, uniformly spraying an antibacterial agent solution on the mixed particles B2, placing the particles in a vacuum drying oven to be dried after the spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C2.
The mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C2 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C2, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; and manufacturing a color comparison card according to the corresponding RGB value.
The method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real object Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition, and if so, showing that the RGB value of the photo of the shot cat litter is not different.
Example 5
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 80 parts of modified fine-pore silica gel, 8 parts of diatomite, 8 parts of activated carbon, 120 parts of urine protein indicator and 0.3 part of antibacterial agent; the urine protein indicator is a bromophenol blue reagent.
The bromophenol blue reagent is prepared by the following method: 0.67g of bromophenol blue is dissolved in 10ml of 0.1mol/L NaOH solution and distilled water is added to 1000 ml.
The modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000ml of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: weighing 0.67g of bromophenol blue, dissolving in 10ml of 0.1mol/L NaOH solution, and adding distilled water to 1000 ml;
(4) weighing modified porous silica gel and bromophenol blue urine protein indicator according to a ratio, soaking the modified porous silica gel in bromophenol blue urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing in a vacuum drying oven for vacuum drying to obtain a primary finished product A2;
(5) mixing the diatomite, the activated carbon and the primary finished product A2 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B2;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; and (3) placing the mixed particles B2 obtained in the step (A) in a rotating disc, uniformly spraying an antibacterial agent solution on the mixed particles B2, placing the particles in a vacuum drying oven to be dried after the spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C2.
The mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(2) photographing the finished cat litter C2 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C2, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; and manufacturing a color comparison card according to the corresponding RGB value.
The method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real world Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition or not, and if so, indicating that the RGB value of the photo of the shot cat litter is not different.
Example 6
The cat litter with the pet urine protein early warning function is prepared from the following raw materials in parts by weight: 100 parts of modified fine-pore silica gel, 10 parts of diatomite, 10 parts of activated carbon, 150 parts of urine protein indicator and 0.5 part of antibacterial agent; the urine protein indicator is a bromophenol blue reagent.
The bromophenol blue reagent is prepared by the following method: 0.67g of bromophenol blue is dissolved in 10ml of 0.1mol/L NaOH solution and distilled water is added to 1000 ml.
The modified fine-pore silica gel is prepared by the following method:
(1) soaking the silica gel particles in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, and drying in a vacuum drying oven at 35-40 ℃ for 30min for later use;
(2) and (2) soaking the silica gel particles obtained in the step (1) in ethyl acetate for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and curing at 37 ℃ for 30min to obtain the modified fine-pore silica gel particles.
The antibacterial agent is polyhexamethylene biguanide hydrochloride. Polyhexamethylene biguanide hydrochloride, also known as PHMB, is available from Shanghai high-polymer biosciences, Inc. and has an active substance content of 20%.
A preparation method of cat litter with a pet urine protein early warning function comprises the following steps:
(1) pretreatment: adding 20ml of 0.2mol/L Na2HPO4 solution into 1000m1 of 0.1mol/L citric acid solution, and adjusting the pH to 2.1 to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: preparing a bromophenol blue reagent, namely weighing 0.67g of bromophenol blue, dissolving the bromophenol blue in 10ml of 0.1mol/L NaOH solution, and adding distilled water to 1000 ml;
(4) weighing modified porous silica gel and bromophenol blue urine protein indicator according to a ratio, soaking the modified porous silica gel in bromophenol blue urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing in a vacuum drying oven for vacuum drying to obtain a primary finished product A2;
(5) mixing the diatomite, the activated carbon and the primary finished product A2 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B2;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; and (3) placing the mixed particles B2 obtained in the step (A) in a rotating disc, uniformly spraying an antibacterial agent solution on the mixed particles B2, placing the particles in a vacuum drying oven to be dried after the spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C2.
The mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
In the step (3), the temperature of the vacuum drying oven is 100 ℃, and the drying time is 12 hours.
When the cat litter with the pet urine protein early warning function is used, a color comparison card can be manufactured for convenience of use so as to quickly compare color changes. The color chart can be prepared by the following method:
(1) photographing the finished cat litter C2 and importing the photographed cat litter into a computer; taking urine protein overproof cat urine and normal cat urine to respectively soak finished cat litter C2, taking a picture of a color change result, guiding the picture into a computer, carrying out color difference inspection on the picture in the computer, and analyzing to obtain corresponding RGB values; and manufacturing a color comparison card according to the corresponding RGB value.
The method for detecting the chromatic aberration comprises the following steps:
(1) generating an electronic Lauer color comparison card in a computer according to the RGB values of all colors in the Lauer color comparison card;
(2) placing the cat litter to be photographed and the real object Lauer colorimetric card together, photographing in the same environment, and then importing the photographed cat litter and the real object Lauer colorimetric card into a computer; and then verifying whether the RGB value of the real object Lauer colorimetric card is consistent with the RGB value of the standard Lauer colorimetric card of the electronic edition, and if so, showing that the RGB value of the photo of the shot cat litter is not different.
Application test
Preparing a standard colorimetric card: normal cat urine protein values were 15mol/dL, and urine solutions containing 10 mol/dL, 15mol/dL, 20 mol/dL, and 25 mol/dL of urine were selected to prepare color charts as described in examples 1-6, wherein clear water was used as a blank control, and the color charts were prepared with a gradual color change. Wherein, the colorimetric card prepared by using the biuret reagent as the protein indicator is shown in figure 1. When the color changes to purple and is similar to the 15-20 grades, the abnormal urine protein is indicated. The vigilance should be improved. In the same way, a standard colorimetric card taking a bromophenol blue reagent as a protein indicator can be prepared.
The litters obtained in examples 1-6 of the present invention and commercially available ordinary silica gel litters were subjected to urine test experiments. Selecting 35 sick cats with abnormal renal function and urine protein higher than normal value, randomly dividing the sick cats into 7 groups, and respectively using S1-S6 and commercial common cat litters for the invention of examples 1-6 and S7; 35 cats with normal physiological indexes were selected and randomly divided into 7 groups, and commercially available cat litters were used in T1-T6 according to examples 1-6 and T7 of the present invention, respectively.
Statistical performance data, as shown in table 1 below:
TABLE 1 comparison of the Performance of cat litters of the invention with commercial litters
Figure 304333DEST_PATH_IMAGE001
Compared with the commercially available common cat litter, the embodiment of the invention has high urine absorption speed, the shortest time can reach 13 seconds, and the commercially available cat litter needs more than 50 seconds; meanwhile, the time for dehydrating and hardening the excrement is only about 200 seconds, which is far less than 400 seconds of the cat litter sold on the market. And the capability of absorbing the peculiar smell is relatively better. Presumably, the silica gel has good hydrophilic modification effect, so that the protein indicator is fully impregnated in the silica gel, abnormal urine of urine protein has color reaction, and normal urine has no color reaction, thereby helping pet raising personnel preliminarily know the health condition of pets and playing a warning role.
It should be noted that the above-mentioned embodiments are only some of the preferred modes for implementing the invention, and not all of them. Obviously, all other embodiments obtained by persons of ordinary skill in the art based on the above-mentioned embodiments of the present invention without any creative effort shall fall within the protection scope of the present invention.

Claims (4)

1. The cat litter with the pet urine protein early warning function is characterized by being prepared from the following raw materials in parts by weight: 60-100 parts of modified fine-pore silica gel, 5-10 parts of diatomite, 5-10 parts of activated carbon, 100-150 parts of urine protein indicator and 0.1-0.5 part of antibacterial agent; the urine protein indicator is a bromophenol blue reagent or a biuret reagent;
the preparation method of the cat litter comprises the following steps:
(1) pretreatment: 0.2mol/L Na is added into 1000m1 of 0.1mol/L citric acid liquid2HPO4Adjusting the pH value of the solution to be 2.1 by 20ml to prepare a buffer solution; soaking the fine-pore silica gel in hydrochloric acid solution for 30min, taking out, washing with distilled water for 3-5 times, soaking in the obtained buffer solution for 30min, taking out, washing with distilled water for 3-5 times, and air drying;
(2) preparing modified fine-pore silica gel: soaking the silica gel particles obtained in the step (1) in an ethanol solution with the mass fraction of 60%, ultrasonically cleaning for 30min, cleaning with distilled water, placing in a vacuum drying oven for drying at 35-40 ℃ for 30min, soaking the silica gel particles in an ethyl acetate solution for 10-15min, taking out, soaking in a polycarbodiimide solution with the mass fraction of 15% for 2min, and then curing at 37 ℃ for 30min to obtain modified fine-pore silica gel particles;
(3) preparing a urine protein indicator: preparing a biuret reagent, weighing 1.5g of copper sulfate and 6.0g of potassium sodium tartrate, dissolving with 500mL of distilled water, adding 300mL of 10% sodium hydroxide solution under stirring, and diluting with water to 1L; preparing a bromophenol blue reagent, namely weighing 0.67g of bromophenol blue, dissolving the bromophenol blue in 10ml of 0.1mol/L NaOH solution, and adding distilled water to 1000 ml;
(4) weighing modified pore silica gel and biuret urine protein indicator according to a ratio, soaking the modified pore silica gel in biuret urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing the silica gel particles in a vacuum drying oven for vacuum drying to obtain a primary finished product A1; weighing modified porous silica gel and bromophenol blue urine protein indicator according to a ratio, soaking the modified porous silica gel in bromophenol blue urine protein indicator solution, stirring, heating and stirring at 50 ℃ for 2-5h, filtering to separate out silica gel particles, and placing in a vacuum drying oven for vacuum drying to obtain a primary finished product A2;
(5) mixing the diatomite, the activated carbon and the primary finished product A1 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B1;
(6) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; placing the mixed particles B1 obtained in the step (5) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C1;
(7) mixing the diatomite, the activated carbon and the primary finished product A2 obtained in the step (4) according to the weight, and then placing the mixture into a stirrer for homogenization to obtain mixed particles B2;
(8) dissolving the antibacterial agent in 50-100 times of distilled water by weight to obtain an antibacterial agent solution; and (3) placing the mixed particles B2 obtained in the step (7) in a rotating disc, uniformly spraying an antibacterial agent solution on the rotating disc, placing the particles in a vacuum drying oven for drying after spraying is finished until the water content is 4-8%, and then packaging to obtain the finished cat litter C2.
2. The cat litter with pet urine protein warning function as claimed in claim 1, wherein the antibacterial agent is polyhexamethylene biguanide hydrochloride.
3. The cat litter with the pet urine protein early warning function as claimed in claim 1, wherein the mass fraction of the ethyl acetate solution in the step (2) is 60-80%.
4. The cat litter with the pet urine protein early warning function according to claim 1, wherein the temperature of the vacuum drying oven in the step (4) is 100 ℃ and the drying time is 12 hours.
CN201811247499.0A 2018-10-25 2018-10-25 Cat litter with pet urine protein early warning function and preparation method thereof Active CN109287499B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811247499.0A CN109287499B (en) 2018-10-25 2018-10-25 Cat litter with pet urine protein early warning function and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811247499.0A CN109287499B (en) 2018-10-25 2018-10-25 Cat litter with pet urine protein early warning function and preparation method thereof

Publications (2)

Publication Number Publication Date
CN109287499A CN109287499A (en) 2019-02-01
CN109287499B true CN109287499B (en) 2020-05-12

Family

ID=65158678

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811247499.0A Active CN109287499B (en) 2018-10-25 2018-10-25 Cat litter with pet urine protein early warning function and preparation method thereof

Country Status (1)

Country Link
CN (1) CN109287499B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112715385B (en) * 2020-12-30 2023-06-30 青岛美今生物科技有限公司 Preparation method of functional chromogenic health indication plant deodorizing cat litter
CN112790113A (en) * 2021-01-15 2021-05-14 上海毛球日记宠物用品有限公司 Water-absorbing color-changing cat litter convenient to clean and preparation method thereof
CN116953258A (en) * 2023-08-02 2023-10-27 山东瑞达硅胶有限公司 Pet urine protein detection particle and preparation method thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101140278B (en) * 2007-11-05 2012-01-11 刘世安 Preparation method of animals urine checking granule
CN107206350B (en) * 2014-10-01 2020-05-01 7905122加拿大股份有限公司 Method and device for producing water-absorbing material and use in cat litter
CN104472372A (en) * 2014-11-18 2015-04-01 芜湖悠派卫生用品有限公司 Fen-flavor cat litter and preparation method thereof
JP6754287B2 (en) * 2016-12-05 2020-09-09 花王株式会社 Pet litter box
CN108476991A (en) * 2018-03-13 2018-09-04 长兴么么派宠物用品有限公司 A kind of production method of pure natural green tea pine cat litter

Also Published As

Publication number Publication date
CN109287499A (en) 2019-02-01

Similar Documents

Publication Publication Date Title
CN109287499B (en) Cat litter with pet urine protein early warning function and preparation method thereof
CN1264008C (en) Moisture indicators for the absorbent capacity of a dessicant
JP5099380B2 (en) Antiallergen
CN104254346B (en) Gaseous aldehyde deodorant and its manufacture method
Hu et al. Equilibrium and kinetics of aniline adsorption onto crosslinked sawdust-cyclodextrin polymers
US8540945B2 (en) Water absorbing material and manufacturing method therefor
CN108318477A (en) Based on TiO2Electrogenerated chemiluminescence probe prepared by metal organic frame and its competitive type immuno-sensing method to vomitoxin
US9012233B2 (en) Water absorbing material
AU2237600A (en) Quick acting toxic ammonia test for aqueous samples
WO2005071420A1 (en) Method of protein measurement
CN101687118B (en) Solid phase extraction of ochratoxins
CN114617069B (en) Functional bio-based cat litter capable of detecting diseases of cat urinary system
CN111729655A (en) Color-changing adsorption material capable of repeatedly and continuously adsorbing formaldehyde and preparation method thereof
JPWO2012050156A1 (en) Antiallergen
CN113439669B (en) Functional color development health indication and deodorization high-performance mixed cat litter and preparation method thereof
CN1940536A (en) Method gas content determining kit and its use
US20170333588A1 (en) Deodorant, deodorant composition, and deodorizing product
CN107159157A (en) Contain heavy metal ion blotting cross-linked chitosan nano fibrous membrane and preparation method thereof
JPWO2004015423A1 (en) Protein measuring method, protein measuring indicator, and protein measuring test piece
CN112730563B (en) Preparation method of sulfaquinoxaline electrochemical aptamer sensor based on internal circulation amplification strategy
WO2009005936A1 (en) Accelerating a ninhydrin reaction
JPS5839950A (en) Test kit for measuring bilirubin and measuring method using said kit
CA2586587A1 (en) Method of determining tropomyosin in chitosan
JP2002200149A (en) Deodorant
WO2004015424A1 (en) Test piece for protein assay and process for producing the same

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210914

Address after: 300110 1-1-505-1, Xindu building, southwest of the intersection of Weijin road and wandezhuang street, Nankai District, Tianjin

Patentee after: HUIJIAWANG (TIANJIN) TECHNOLOGY Co.,Ltd.

Address before: 276000 west side of north section of Industrial Road, Lanshan District, Linyi, Shandong

Patentee before: LINYI University

Effective date of registration: 20210914

Address after: 201807 floor 2, building 1, No. 1104, Jiatang Road, Jiading Industrial Zone, Jiading District, Shanghai

Patentee after: SHANGHAI LIKANG BIOLOGICAL HIGH-TECH Co.,Ltd.

Address before: 300110 1-1-505-1, Xindu building, southwest of the intersection of Weijin road and wandezhuang street, Nankai District, Tianjin

Patentee before: HUIJIAWANG (TIANJIN) TECHNOLOGY Co.,Ltd.

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20221027

Address after: 200436 Room 302, Building 3, No. 39, Lane 1861, Hutai Road, Baoshan District, Shanghai

Patentee after: Maidu Chongyi (Shanghai) Technology Development Co.,Ltd.

Address before: 201807 floor 2, building 1, No. 1104, Jiatang Road, Jiading Industrial Zone, Jiading District, Shanghai

Patentee before: SHANGHAI LIKANG BIOLOGICAL HIGH-TECH Co.,Ltd.