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HG 3297-2001 Fosetyl aluminum wettable powder

Basic Information

Standard ID: HG 3297-2001

Standard Name: Fosetyl aluminum wettable powder

Chinese Name: 三乙膦酸铝可湿性粉剂

Standard category:Chemical industry standards (HG)

state:in force

Date of Release2002-01-24

Date of Implementation:2002-07-01

standard classification number

Standard ICS number:Agriculture>>65.100 Pesticides and other agricultural chemical products

Standard Classification Number:Chemicals>>Fertilizers, Pesticides>>G25 Pesticides

associated standards

alternative situation:HG 3297-1989 (original standard number ZB G25009-89)

Publication information

other information

Focal point unit:National Industrial Automation System Standardization Committee

Introduction to standards:

HG 3297-2001 Aluminum fosetyl wettable powder HG3297-2001 Standard download decompression password: www.bzxz.net

Some standard content:

Chemical Industry Standard of the People's Republic of China
HG3291~3297—2001
(2001)
Published on January 24, 2002
Implemented on July 1, 2002
Published by the State Economic and Trade Commission
Reference number: 10084—2002
IIG 3297.-201
The third and fifth parts of this standard are mandatory, and the rest are recommended. This standard is a derivative of the mandatory chemical industry standard IIC3297-159$triethyl solution. The main technical differences between this standard and HG3297-1180 are: the range of H2O is increased, the actual storage temperature of phosphite and the addition of the cooling control date, and the control date of the acid cost. The analytical method of triethylamine is equivalent to the International Pesticide Analysis Cooperation Committee (1FAC38+/WP/M/(19U3) method. Increase the pH range, industrial phosphorus salt and accelerated storage test determination method. This standard is issued by the former State Petroleum and Chemical Industry Bureau Policy and Regulations Department from the date of implementation. This standard is drafted by the National Pesticide Standardization Technical Committee 1. This standard is drafted by: Shenyang Chemical Industry Research Institute, and the participating units are: Shandong Dawei Pesticide Co., Ltd., Zhenjiang Jiangnan Chemical Plant. The main people of this standard are Zhang Bulong, Jie Yankun, and Gong Baojie. This standard was first issued as a professional standard in 1980, and was converted into a regulatory chemical industry standard in 1990 and renumbered as TIG. .297$8S.
This standard is managed by the National Standardization Technical Committee of the National Coatings Standardization Technical Committee.5.
Chemical Industry Standard of the People's Republic of China
Aluminum triethylphosphinate wettable powder
Fngetyl-aluminium Wrttable: Powlers Medical Household·Pao has a teaching branch (. The common name of the ship is you, the comprehensive structure and cost physicochemical parameters are as follows: Iy Common name Fogetyl-nluuinimfeyACIPAC code: 384
Chemical name: Tri (acetic phosphinoic acid) Zhi
Synthesis average:
Experimental ratio CHAIOP
Relative molecular weight, 351,-1 (according to 19074 international deduction for atomic mass) Biological activity: Nan
Tower decomposition point 200
Steam R (a5% Pa
HG3297-2 001
BHC$2071989
(24/1): 129 in water: 920 in acetic acid: 45 ... The following standards contain clauses that, through the use of the same format in this standard, become the clauses of this standard: When this standard is published, the versions indicated are still valid. All standards will be revised. The parties to this standard should explore the possibility of using the following standards to develop new versions: B/T6U-192 Preparation of non-titrating wave for chemical reagent titration analysis (single analysis) T-Preparation of preparations and products used in chemical reagent test methods GB168 Preparation of medicinal liquors in China
e1-1 Method for determination of pesticide values ​​
GBT11493 Commercial packaging materials
G/T16G8730198 9)Commodity agricultural products hot fork sampling method G537951999 Packaging rules for pesticides
(G5/1515-:333 Method for determination of wettability of pesticides Approved by China Economic and Trade Commission on January 24, 2002, implemented on July 1, 2002
HG3297-2001
Determination of wettability of pesticides by floating force method
GR14825-
(GB/=16150995 Pesticide powders, determination method of wettability of wettable powders 3 Requirements
3.1 Appearance: Colorless or off-white loose powder, without lumps. 3.2 The wettability of calcium triacetate is in accordance with the requirements of Table 1. Table 1 The control items of calcium triacetate are as follows: Table 1 The content of calcium triacetate is the maximum value of acetic acid, the non-acid salt (calculated by toxicity), the suspension rate, the shrinkage (by. The time of lubrication, the test method of the test will be less than three months. 4.1 Sampling According to the sampling method of GB/T1635145, the sampling of the packaging is determined by the random number table method, and the sampling plate should be less than fzc g.
4.2 Identification test
4.2. Acid chromatography
Use a detector with a negative charge to measure the negative charge of the sample. Under the condition of the chromatographic end of the phase, the relative difference between the retention time of a certain sample in the sample solution and the peak time of a certain calcium acetyl phosphate in the standard solution is within 1.5%. Conditions:
Weigh the sample and dissolve it in a 10mL volumetric flask, add 20% water, and produce 3rmu in an ultrasonic filter water bath, cool to room temperature, use a dynamic filter, and filter with 0.2 % ionizer before analysis. Sample reduction: Weigh the sample containing about 7.1% acetic acid in a 1UmL volumetric flask, and the other standard solutions are connected. The mobile phase is 0.1425 Nt.HO, and n. 108 g NaCO,- add water to 1 L. Hoop phase also potential: with commercial exchange color harmonic conductivity detector, containing Sar-Ion A3cc (particle size Em), ommxt.Bmm (id housing, equipped with pre-column. Soft wave water bath
filter: .?um diameter,
flow rate: 0. 8 ml.min:
Formula: air,
batch preparation, electronic control or chemical inhibition formula (TIS()) = 0.25mol:/L, flow rate 4ml./mis acid inhibition 710.
Retain the call about i
4.2.2 Infrared spectroscopy
Separate the triethylamine melt and filler, prepare a sample and a sample of KBr jade pieces (triethylamine Oh cry sample or standard 55
IC3297-2001
sample 1mg and K35umg, scan the film from 40U-4U, test There should be no difference in the amount of sample and standard sample (see Figure 1).
Figure 1 Spectrum of triethylamine standard
4.3 Determination of aluminum triacetate content
4.3.1 Method summary
Ethyl acetate is heated in a double emulsion to alkaline hydrolysis to produce an acid. The excess amount of acetic acid should be small. The reaction formula is:
CHAIO, F.+30H
HPO—I
4.3.2 Reagents and liquids
Acetic acid.
Potassium hydroxide.
Acid solution: 80%.
Acid hydrolysis solution: 11,50,=2 ml/
Acid condensate: N=/.
Hydrogen hydration agent B solution (NaH) 0.1tl.
Current standard with slight reduction;cc
-SHPO +R: H,OH. AI
-HPC+21
-S, CK+21
I=0. 1 ol/L,GK/ 601 Preparation of standard titration solution of sodium sulfate: (Na2SO4) (Na2SO4) (>: o.1mnl/I..c [/T6u Preparation: Indicator: 1GB/03 Preparation,
Precipitate the fresh preparation of the indicator
Destroy the paint solution: 2H-7.8 = 0.2, weigh 1C sodium oxide accurately to U.UUO2> Dissolve in 1.3L water towel, add phosphoric acid drop liquid and neutralize it = X, Ling cool to temperature under the preparation of commercial acid limit H:, humanized and standard tour minus m stir to dissolve in water to 2T, keep at room temperature, and then drip it again The paper acid is oxidized and the rate of oxidization is determined to be zero. Potentiometric titration is performed by ultrasonication of the liquid in a water bath. pH J. Adjustable electric heating jacket: 200. Ball tower condensation, iodine volume bottle: 0ml. County irradiation. 4.3.4 Determination steps 4.3.4.1 Sample Rong Xiao HC3297-2001 Weigh the sample containing about 3% of the mold brand oxidized (the oxidized sample is correct and placed in.Into the volumetric flask, add 200ml sodium iodine oxide liquid, cool to the room temperature in a water bath, and set the volume limit to sodium oxide A. Use a thermometer to transfer 10L of the sample to a 25L iodine volumetric flask, add 40L sodium oxide A liquid, connect it to the cooling tube, and fill it up to 15. Rinse the condenser with a small amount of water and cool to room temperature. At the same time, add 2 drops of acid indicator when it is close to the end point, and the red stain disappears. 4.3.4.2 Add 25 mL of standard buffer and 11 mL of standard centrifuge to the micro-swirler. Put the stopper on the bottle to mix, add water and place the bottle in a dark place at 3°C ​​for 45 min. Acidify with 100 mL of ethyl acetate and titrate with molten sulfuric acid. When near the end point, add 3 mL of vortex indicator. The disappearance of the negative titration curve is the end point (or the end point can be determined by potential reduction). 4.3.4.3 Replace the sample with sodium hydroxide under the same conditions and use the remaining sample for determination. 4.3.5 Calculate the mass fraction x in the test sample, %>, using formula (1): -s.059 x 100.x o.1
×1C/590
The volume of sulfuric acid consumed by a drop of the titration lamp, ml Wherein, V—
The volume of sulfuric acid consumed by the titration lamp, mL: The actual concentration of sulfuric acid standard titration solution, aol/yuan: Sample mass, 8
The mass of 1.00ml of 1.0001ml/T equivalent to 1.00ml of standard titration solution (N%).
4.3.6 The allowable difference
The difference between the results of two determinations shall not be greater than 1.3% for wettable powder and not greater than 0.6% for 4% for wettable powder. The average value shall be taken as the determination result.
4.4 Determination of nitrite
4.4. 1 Methods: According to the individual characteristics of the components, the product is added with a5% dropwise addition, 4.4.2 and the reagent and expansion are the same as 4.3.2. 4.4.3 Apparatus 4.4.4 Determination steps 4.4.4.1 Test solution: About 82ml of the test solution containing 300 ethyl acetate (300 ethyl acetate) is placed in a 150ml filter cup and stirred with 10 mic. Add about 5ml of hydroxylated A. Under the control of a pH meter, add dropwise HC32972001 until the pH reaches -7.3, less than 0.2, and transfer to 250ml of the measuring instrument with water. 4.4.4.2 Determination Same as 4.3.4. 4.4.4.3 Empty chamber determination Under the same sterilization conditions, use m1.5% of the selected solution and reduce the sample by the same amount as 4.3.1.2. 4.4.5 Calculate the number of liters of phosphorus oxide (calculated as aluminum suboxide) X (%). Calculate according to formula (2): X = V - VX 0.052 95
The volume of sodium thiosulfate standard titration solution consumed by the sample is ml. The actual volume of sodium thiosulfate standard titration solution consumed by the sample is ml/L; the actual volume of sodium thiosulfate standard titration solution is 1.0ml/L: Test standard mass:
titrate with 1.0mL sodium thiosulfate standard titration solution (NSO, = 1.0ml/L and the mass of the energy expressed in grams
4.5PH value determination
According to GB/T16U1-1S93\powder test. 4. 6 Determination of suspension rate
Weigh about 100 g of triethylamine (accurate to 0.02) according to B142. Transfer the remaining 25% to a 250 ml iodine dish, wash the residue with a small amount of water and transfer it to a volumetric flask. Add 25 mL of sodium hydride solution (>H> ?al/1.0), boil and reflux with condenser for 1 hour, and proceed with the rest as in 4.3.4. 4.7 Determination of temperature
According to G1615
4.8 Determination of immersion time
According to GB5451:
4.9 Accelerated storage test
4.9.1 Summary of method
The product performance changes after aging are predicted by thermal aging test. 4.9. 2[Clinical
oven: 12℃
outside: 210aL inner diameter e~.6.5m
round blood: light and large heart grams matched with beaker, just produce 2.45V2 average pressure inside, 4.9.3 test
put the test column into the cup, without any force, make it vinegar into a uniform thickness of the ruler. Press the plate on the sample, put the cup into the box, store 14c at 512 ten, put the bottom into the dry In a deep container, cool to the desired temperature. Within 4 hours, complete the micro-determination of the effective ingredient content and the difference between the two. The determination results shall meet the requirements of the table 4.10 Inspection and acceptance of products
Inspection and acceptance of products shall comply with the provisions of GR/T1E4. The limit value processing shall adopt the approximate value comparison method. 5 Marking, labeling, packaging, storage and transportation
5.12 Packaging requirements The marking, labeling, packaging and storage of powders shall comply with GB3795 5.2 The whole rack of ethyl acetate wet cleaner should be packaged in plastic (polyethylene outer layer, high pressure polyethylene inner layer) or aluminum package, 59
HG3297-·2001
The net content of ethyl acetate wet cleaner is 1581, and then packed into plastic box. The content of the plastic box should not exceed 1581. 5.3 According to the requirements of the contract, the form of delivery should be used. The packaging and supply should meet the requirements of 4!6. 5.4 Packaging properties: There is a ventilated environment in the warehouse. 5.5 Storage and transportation: Strictly avoid moisture, rain, and exposure to the sun. Keep the storage environment well ventilated. Do not mix with food, chemicals, and materials. Avoid contact with skin.
5.6 This product is an organic repellent, which is low in toxicity to humans and animals, safe to animals, and non-irritating to the skin and eyes. It is non-toxic. If women are poisoned, they should go to the hospital for examination and treatment in time. When using this product, you should wear protective gloves, masks, and clean protective clothing. After use, wash with water.
5.7 Storage conditions: From the date of production, the warranty period of aluminum wettable powder is two years.Under the control of pH meter, add HC32972001 of hydrogen peroxide dropwise to the pH value of -7.3. 0.2 or less, and transfer 250ml of water to the sample for calculation. 4.4.4.2 Determination of hydrogen peroxide Same as 4.3.4. 4.4.4.3 Determination of hydrogen peroxide Under the same pH condition, replace the solution with 1ml of hydrogen peroxide and reduce the sample with the same pH value as 4.3.1.2. 4.4.5 Calculate the base number X (in liters of aluminum suboxide) of the test sample. Calculate X = V-VX 0.052 according to formula (2). 95
The volume of sodium thiosulfate standard titration solution consumed by the sample is ml. The actual volume of sodium thiosulfate standard titration solution consumed by the sample is ml/L; the actual volume of sodium thiosulfate standard titration solution is 1.0ml/L: Test standard mass:
titrate with 1.0mL sodium thiosulfate standard titration solution (NSO, = 1.0ml/L and the mass of the energy expressed in grams
4.5PH value determination
According to GB/T16U1-1S93\powder test. 4. 6 Determination of suspension rate
Weigh about 100 g of triethylamine (accurate to 0.02) according to B142. Transfer the remaining 25% to a 250 ml iodine dish, wash the residue with a small amount of water and transfer it to a volumetric flask. Add 25 mL of sodium hydride solution (>H> ?al/1.0), boil and reflux with condenser for 1 hour, and proceed with the rest as in 4.3.4. 4.7 Determination of temperature
According to G1615
4.8 Determination of immersion time
According to GB5451:
4.9 Accelerated storage test
4.9.1 Summary of method
The product performance changes after aging are predicted by thermal aging test. 4.9. 2[Clinical
oven: 12℃
outside: 210aL inner diameter e~.6.5m
round blood: light and large heart grams matched with beaker, just produce 2.45V2 average pressure inside, 4.9.3 test
put the test column into the cup, without any force, make it vinegar into a uniform thickness of the ruler. Press the plate on the sample, put the cup into the box, store 14c at 512 ten, put the bottom into the dry In a deep container, cool to the desired temperature. Within 4 hours, complete the micro-determination of the effective ingredient content and the difference between the two. The determination results shall meet the requirements of the table 4.10 Inspection and acceptance of products
Inspection and acceptance of products shall comply with the provisions of GR/T1E4. The limit value processing shall adopt the approximate value comparison method. 5 Marking, labeling, packaging, storage and transportation
5.12 Packaging requirements The marking, labeling, packaging and storage of powders shall comply with GB3795 5.2 The whole rack of ethyl acetate wet cleaner should be packaged in plastic (polyethylene outer layer, high pressure polyethylene inner layer) or aluminum package, 59
HG3297-·2001
The net content of ethyl acetate wet cleaner is 1581, and then packed into plastic box. The content of the plastic box should not exceed 1581. 5.3 According to the requirements of the contract, the form of delivery should be used. The packaging and supply should meet the requirements of 4!6. 5.4 Packaging properties: There is a ventilated environment in the warehouse. 5.5 Storage and transportation: Strictly avoid moisture, rain, and exposure to the sun. Keep the storage ventilated. Do not mix with food, chemicals, and materials. Avoid contact with skin.
5.6 This product is an organic repellent, which is low in toxicity to humans and animals, safe to animals, and non-irritating to skin and eyes. It is non-toxic. If women are poisoned, they should go to the hospital for examination and treatment in time. When using this product, you should wear protective gloves, masks, and clean protective clothing. After use, wash with water.
5.7 Storage conditions: From the date of production, the warranty period of aluminum wettable powder is two years.Under the control of pH meter, add HC32972001 of hydrogen peroxide dropwise to the pH value of -7.3. 0.2 or less, and transfer 250ml of water to the sample for calculation. 4.4.4.2 Determination of hydrogen peroxide Same as 4.3.4. 4.4.4.3 Determination of hydrogen peroxide Under the same pH condition, replace the solution with 1ml of hydrogen peroxide and reduce the sample with the same pH value as 4.3.1.2. 4.4.5 Calculate the base number X (in liters of aluminum suboxide) of the test sample. Calculate X = V-VX 0.052 according to formula (2). 95
The volume of sodium thiosulfate standard titration solution consumed by the sample is ml. The actual volume of sodium thiosulfate standard titration solution consumed by the sample is ml/L; the actual volume of sodium thiosulfate standard titration solution is 1.0ml/L: Test standard mass:
titrate with 1.0mL sodium thiosulfate standard titration solution (NSO, = 1.0ml/L and the mass of the energy expressed in grams
4.5PH value determination
According to GB/T16U1-1S93\powder test. 4. 6 Determination of suspension rate
Weigh about 100 g of triethylamine (accurate to 0.02) according to B142. Transfer the remaining 25% to a 250 ml iodine dish, wash the residue with a small amount of water and transfer it to a volumetric flask. Add 25 mL of sodium hydride solution (>H> ?al/1.0), boil and reflux with condenser for 1 hour, and proceed with the rest as in 4.3.4. 4.7 Determination of temperature
According to G1615
4.8 Determination of immersion time
According to GB5451:
4.9 Accelerated storage test
4.9.1 Summary of method wwW.bzxz.Net
The product performance changes after aging are predicted by thermal aging test. 4.9. 2[Clinical
oven: 12℃
outside: 210aL inner diameter e~.6.5m
round blood: light and large heart grams matched with beaker, just produce 2.45V2 average pressure inside, 4.9.3 test
put the test column into the cup, without any force, make it vinegar into a uniform thickness of the ruler. Press the plate on the sample, put the cup into the box, store 14c at 512 ten, put the bottom into the dry In a deep container, cool to the desired temperature. Within 4 hours, complete the micro-determination of the effective ingredient content and the difference between the two. The determination results shall meet the requirements of the table 4.10 Inspection and acceptance of products
The inspection and acceptance of products shall comply with the provisions of GR/T1E4. The limit value processing shall adopt the approximate value comparison method. 5 Marking, labeling, packaging, storage and transportation
5.12 Packaging requirements The marking, labeling, packaging and storage of powders shall comply with GB3795 5.2 The whole rack of ethyl acetate wet cleaner should be packaged in plastic (polyethylene outer layer, high pressure polyethylene inner layer) or aluminum package, 59
HG3297-·2001
The net content of ethyl acetate wet cleaner is 1581, and then packed into plastic box. The content of the plastic box should not exceed 1581. 5.3 According to the requirements of the contract, the form of delivery should be used. The packaging and supply should meet the requirements of 4!6. 5.4 Packaging properties: There is a ventilated environment in the warehouse. 5.5 Storage and transportation: Strictly avoid moisture, rain, and exposure to the sun. Keep the storage ventilated. Do not mix with food, chemicals, and materials. Avoid contact with skin.
5.6 This product is an organic repellent, which is low in toxicity to humans and animals, safe to animals, and non-irritating to skin and eyes. It is non-toxic. If women are poisoned, they should go to the hospital for examination and treatment in time. When using this product, you should wear protective gloves, masks, and clean protective clothing. After use, wash with water.
5.7 Storage conditions: From the date of production, the warranty period of aluminum wettable powder is two years.
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