NITRIC ACID 58-62 Percent
- Part number
- RXSOL-19-1542-045
- Category
- Agriculture
- Brand
- RXSOL
Overview
Nitric acid 58-62% concentration frequently used in the production of fertilizers and also most commonly used for metal treatment as well as used in various industrial and laboratory applications. NITRIC ACID is a corrosive, oxidizing liquid.
Applications
What is passivation?
The "passivation" process removes iron residues and probably forms an oxide layer that boosts the corrosion resistance of the stainless steel.
According to ASTM A380, passivation is "the removal of exogenous iron or iron compounds from the surface of stainless steel by means of a chemical dissolution, most typically by a treatment with an acid solution that will remove the surface contamination, but will not significantly affect the stainless steel itself." In addition, it also describes passivation as "the chemical treatment of stainless steel with a mild oxidant, such as a nitric acid solution, for the purpose of enhancing the spontaneous formation of the protective passive film."
In lay terms, the passivation process removes "free iron" contamination left behind on the surface of the stainless steel from machining and fabricating. These contaminants are potential corrosion sites that result in premature corrosion and ultimately result in deterioration of the component if not removed. In addition, the passivation process facilitates the formation of a thin, transparent oxide film that protects the stainless steel from selective oxidation (corrosion). So what is passivation? Is it cleaning? Is it a protective coating? It is a combination of both.
GENERAL PASSIVATION METHOD
To effectively passivate the free-machining stainless steels, Carpenter has developed the A-A-A (alkaline-acid-alkaline) process that neutralizes trapped acid. This method of passivation can be accomplished in less than 2 hours. Here is the step-by-step procedure:
After degreasing, soak the parts for 30 minutes in a 5 percent solution of sodium hydroxide at 160[degrees]F to 180[degrees]F (71[degrees]C to 82[degrees]C). Then rinse the part thoroughly in water. Next, immerse the part for 30 minutes in a 20 percent-by-volume nitric acid solution containing 3 ounces per gallon (22 g/liter) of sodium dichromate at 120[degrees]F to 140[degrees]F (49[degrees]C to 60[degrees]C). After removing the part from this bath, flush it with water, then immerse it in the sodium hydroxide solution for another 30 minutes. Rinse the part again with water and dry it, completing the A-A-A method. The benefits of this method are shown in Figure 3.
OR
As per ASTM standards For Type 304 stainless steel :::: FIRST OF ALL degrease the parts and then wash them in an alkaline bath for 10 minutes. After 10 minutes the parts are rinsed in clean water before being immersed in a Nitric 2 solution. 20 to 45 volume percent of nitric acid. The parts are then immersed for 30 minutes at a temperature range of 70 to 90 degrees F. They are then rinsed in water left to air dry.
PRECAUTION : 1 > DO avoid chlorides that, in excess, can cause a harmful flash attack. When possible, use only a good grade of water containing less than about 50 parts per million (ppm) of chlorides. Tap water is usually adequate, and in some cases up In several hundred ppm chlorides can be tolerated. 2> Loose iron particles or other foreign particles must be removed or they will appear as rust or stain spots. may become smeared over or imbedded into the surface of corrosion-resistant steel parts.
CITRIC ACID passivation process:
Citric acid passivation has become increasingly popular with manufacturers who want to avoid the use of mineral acids or solutions containing sodium dichromate, along with the disposal problems and greater safety concerns associated with their use. Citric acid is considered environmentally friendly in every respect.
Although citric acid passivation offers attractive environmental advantages, shops having success with mineral acid passivation and suffering no safety issues might want to stay the course. There may be no real need to change if those users have a clean shop, well-maintained and clean equipment, coolant tree of iron-containing shop dirt, and a process that yields good results.
WHY SODIUM DICHROMATE ??
After thorough cleaning, the stainless steel part is ready for immersion in a passivating acid bath. Any one of three approaches can be used--nitric acid passivation, nitric acid with sodium dichromate passivation and citric acid passivation. Which approach to use depends on the grade of stainless steel and prescribed acceptance criteria.
More resistant chromium-nickel grades can be passivated in a 20 percent-by-volume nitric acid bath (Figure 2). As indicated in the same table, less resistant stainless grades can be passivated by adding sodium dichromate to the nitric acid bath to make the solution more oxidizing and capable of forming a passive film on the surface. Another option, used in place of nitric acid plus sodium dichromate, is to increase the concentration of nitric acid to 50 percent-by-volume The sodium dichromate addition and lit : higher nitric acid concentration both reduce the chance of undesirable flash attack.
TEST METHOD for PASSIVATION
Can anyone suggest a simple and quick test which can distinguish between a piece of nitric acid passivated 420 stainless steel and a non-passivated one?
ANSWER : 1 . there is no known simple method to distinguish between a piece of nitric acid passivated 420 stainless steel and a non-passivated one.
ANSWER : 2. Because of the way nitric acid passivation works there is no easy way to test whether it's been done or not. Nitric acid simply dissolves the oxides from the surface and forms a near complete layer of oxide, which protects the underlying metal from further oxidation. Since no chemical is deposited, and it's a relatively weak method of passivation, it would be very hard to test. You can compare panels before and after in a corrosion chamber to see the results, but I'm not sure you could test individual panels and determine whether they had been passivated conclusively.
ANSWER : 3. It was my understanding that you could easily check the passivation status of a part using a solution of copper sulfate and dilute sulfuric acid. An unpassivated part will show copper immersion.
The simple tests for passivation are the acidified copper sulfate test (referred to above) and a ferric cyanide test - both specfified in ASTM ASTM A380 [link is to spec at TechStreet]. These tests are primarily checking for free iron on the surface and cannot confirm that nitric acid passivation has specfically been performed.
How does copper sulfate test for passivation work?
I have heard that a way to check for iron on the surface of a passivated stainless steel part is with the copper sulfate test. From what I can gather the copper replaces the iron due to the fact that the iron is more easily oxidized. Chromium is more easily oxidized than iron, so why doesn't the copper also replace the chromium?
ANSWER : Chromium and nickel will not be replaced with the Copper sulfate test solution (which also contains sulfuric acid), only the Fe or other less noble metals. If there is free iron on the surface it will be replaced by the copper, forming the distinctive copper color on the surface in this 6 minute test.
Of course, this test should only be used on austenitic stainless steel. Some people use it on other grades, but you can get false failures.
How do you separate iron from stainless steel?
Hydrochloric acid. It'll bubble on contact with iron, and eventually dissolve it, allowing you to identify which is which or simply remove the iron. "Stainless Steel" is steel in which most or all of the carbon has been removed.
Dosage and directions
Nitric acid (HNO₃) is a colorless liquid with yellow or red fumes with an acrid odor. Exposure to nitric acid can cause irritation to the eyes, skin, and mucous membrane; it can also cause delayed pulmonary edema, pneumonitis, bronchitis, and dental erosion. Nitric acid is highly corrosive.
Nitric Acid 58 ; Purity/Concentration. 58% ; Form. Liquid ; Chemical Formula. HNO3
Safety and SDS
Read the safety data sheet before handling. Wear suitable gloves and eye protection.
View safety data sheet
| Porduct Name | NITRIC ACID 58-62 percent |
| Part Number | RXSOL-19-1542-045 |
Company Details:
RX MARINE INTERNATIONAL
105, A wing , BSEL , TECH PARK.
VASHI ,NEW BOMBAY 400703 INDIA
Branch : Kandla, Mumbai , Chennai, Vizag, Kolkata, UAE , OMAN , CANADA and KENYA
| Phone | +91 22 20871200 - 1400 |
| Fax | +91 22 27612100 :::AOH :0091 9821214367 |
| rxsolchemicals@gmail.com | |
| Website | www.rxmraine.com |
| Chemical Name | Cas No | EC No | Weight | Formula | Percent | |
| Nitric acid | 7697-37-2 | 231-714-2 | 63,01 g/mol | HNO3 | 58-62 |
| Signal Word | Danger |
| Hazard Statements | H272 May intensify fire; oxidizer. H290 May be corrosive to metals. H314 Causes severe skin burns and eye damage. H330 Fatal if inhaled. |
| Precautionary statements | P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P220 Keep away from clothing and other combustible materials. P280 Wear protective gloves/ protective clothing/ eye protection/ face protection. P303 + P361 + P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water. P304 + P340 + P310 IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/ doctor. P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Supplemental Hazard information (EU) EUH071 Corrosive to the respiratory tract. |
| Classification of the substance or mixture | None |
| Supplemental Hazard Statements | EUH071 Corrosive to the respiratory tract. |
| Other hazards | This substance/mixture contains no components considered to be either persistent, bioaccumulative and toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher. |
| General advice | First aiders need to protect themselves. Show this material safety data sheet to the doctor in attendance. |
| If inhaled | After inhalation: fresh air. Immediately call in physician. If breathing stops: immediately apply artificial respiration, if necessary also oxygen. |
| Eye Contact | After eye contact: rinse out with plenty of water. Immediately call in ophthalmologist. Remove contact lenses. |
| Swallowed | After swallowing: make victim drink water (two glasses at most), avoid vomiting (risk of perforation). Call a physician immediately. Do not attempt to neutralise |
| Skin Contact | In case of skin contact: Take off immediately all contaminated clothing. Rinse skin with water/ shower. Call a physician immediately. |
| Inhalation | None |
| Ingestion | None |
| Most important symptoms and effects, both acute and delaye | The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in section 11 |
| Indication of any immediate medical attention and special treatment needed | No data available |
| Suitable extinguishing media | Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. |
| Unsuitable extinguishing media | For this substance/mixture no limitations of extinguishing agents are given. |
| Special hazards arising from the substance or mixture | Nature of decomposition products not known. Not combustible. Fire may cause evolution of: nitrogen oxides, nitrous gases Has a fire-promoting effect due to release of oxygen. Ambient fire may liberate hazardous vapours. |
| Further information | Suppress (knock down) gases/vapors/mists with a water spray jet. Prevent fire extinguishing water from contaminating surface water or the ground water system. |
|
Hazardous combustion products |
None |
| Advice for firefighters | Stay in danger area only with self-contained breathing apparatus. Prevent skin contact by keeping a safe distance or by wearing suitable protective clothing. |
| Protective Equipment | Use personal protective equipment. |
| Specific Hazards Arising from the Chemical | None |
| Personal precautions, protective equipment and emergency procedures | Advice for non-emergency personnel: Do not breathe vapors, aerosols. Avoid substance contact. Ensure adequate ventilation. Evacuate the danger area, observe emergency procedures, consult an expert. For personal protection see section 8. |
| Spillage | None |
| Personal Protection | None |
| Enviromental Precaution | Do not let product enter drains. |
|
Methods and materials for containment and cleaning |
Cover drains. Collect, bind, and pump off spills. Observe possible material restrictions (see sections 7 and 10). Take up carefully with liquid-absorbent material (e.g. Chemizorb®). Dispose of properly. Clean up affected area |
| Reference to other sections | For disposal see section 13. |
| Advice on protection against fire and explosion | Keep away from open flames, hot surfaces and sources of ignition. |
| Incompatible materials | Keep away from alkalis, strong oxidizing agents and metals. Provide containment walls of adequate capacity to hold any accidental spills. |
| Hygiene measures | Immediately change contaminated clothing. Apply preventive skin protection. Wash hands and face after working with substance. For precautions see section 2.2. |
| Advice on safe handling | Work under hood. Do not inhale substance/mixture. Avoid generation of vapours/aerosols. |
| Conditions for safe storage, including any incompatibilities | No data available |
| Storage conditions | No metal or light-weight-metal containers. No metal containers. Protected from light.Tightly closed. Keep locked up or in an area accessible only to qualified or authorized persons. Separately or together with other oxidising substances only and away from sources of ignition and heat.Because of their oxidation potential these products can raise the burning rate of combustible substances substantially or ignite combustible substances on contact with them. Recommended storage temperature see product label. |
| Storage class | Storage class (TRGS 510): 5.1A: Strongly oxidizing hazardous materials |
| Specific end use(s) | Apart from the uses mentioned in section 1.2 no other specific uses are stipulated |
| Advice on general occupational hygiene | Advice on safe handling Observe label precautions. Change contaminated clothing. Wash hands after working with substance. |
| Exposure controls | Personal protective equipment |
| Engineering Control | None |
| Eye/face protection | Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Tightly fitting safety goggles |
| Body Protection | Acid-resistant protective clothing |
| Skin protection | This recommendation applies only to the product stated in the safety data sheet, supplied by us and for the designated use. When dissolving in or mixing with other substances and under conditions deviating from those stated in EN374 please contact the supplier of CE-approved gloves (e.g. KCL GmbH, D-36124 Eichenzell, Internet: www.kcl.de). Splash contact Material: butyl-rubber |
| Respiratory protection |
Recommended Filter type: Filter E-(P3) The entrepeneur has to ensure that maintenance, cleaning and testing of respiratory protective devices are carried out according to the instructions of the producer. These measures have to be properly documented. Not required; except in case of aerosol formation.
|
| Other Protection Measure | None |
| Control of environmental exposure | Do not let product enter drains. |
| Physical state | Liquid |
| Odour | Stinging |
| Odor Threshold | Not Applicable |
| pH | < 1 at 20 °C |
| Melting Point | -41,59 °C |
| Flash Point | No data available |
| Evaporation Rate | Not Applicable |
| Flammability (solid, gas) | No data available |
| Explosive limits | No Data Available |
| Upper/lower flammability or explosive limits | No data available |
| Autoignition temperature | No data available |
| Decomposition temperature | No data available |
| Vapour pressure | 10 hPa at 20 °C |
| Viscosity | Viscosity, kinematic: No data available Viscosity, dynamic: 0,746 mPa.s at 25 °C |
| Density | 1,9 g/cm3 at 20 °C |
| Relative Density | No data available |
| Specific Gravity | No data available |
| Partition coefficient | No data available |
| Explosive properties | No data available |
| Solubility | 1.000 g/l at 20 °C - soluble, (development of heat) |
| Ignition temperature | No information available. |
| Particle characteristics | No data available |
| Boiling Point | (for product) 185.0 F (85.0 C) @ 760 mmHg |
| Vapor Pressure | (for product) 51.000 mmHg @ 77.00 F |
| Specific Vapor Density | 2.200 @ AIR=1 |
| Specific Gravity | 1.424 @ 77.00 F |
| Liquid Density |
11.850 lbs/gal @ 77.00 F 1.424 kg/l @ 25.00 C |
| Percent Volatiles | 100.0 % |
| Evaporation Rate | SLOWER THAN ETHYL ETHER |
| Appearance | No data |
| State | LIQUID |
| Physical Form | HOMOGENEOUS SOLUTION |
| Color | CLEAR,YEL-RED-BRN, ACRID ODOR |
| Reactivity | strong oxidising agent |
| Chemical stability | Sensitivity to light The product is chemically stable under standard ambient conditions (room temperature) . |
| Possibility of hazardous reactions | Risk of explosion with: Acetone acetonitrile acetylidene Alcohols anilines antimony hydride arsenic hydride organic combustible substances phosphides benzene/benzene derivatives Amines alkenes Halogenated hydrocarbon Ether hydrazine and derivatives Sulfides Dioxane acetic acid Acetic anhydride Flurine |
| Conditions to avoid | May discolor on exposure to air and light. no information available |
| Incompatible materials |
Cellulose, MetalsContact with metals may lead to the formation of nitrous gases and hydrogen.
|
| Hazardous decomposition products | In the event of fire: see section 5 |
| Acute toxicity | Oral: No data available Acute toxicity estimate Inhalation - 4 h - 0,05 mg/l - vapor (Expert judgment) Dermal: No data available |
| Skin corrosion/irritation | Skin - Rabbit Result: Causes severe burns. Remarks: (IUCLID) Remarks: Causes poorly healing wounds |
| Serious eye damage/irritation | Eyes - Rabbit Result: Causes burns. Remarks: (IUCLID) Remarks: Causes serious eye damage. |
| Respiratory or skin sensitization | No data available |
| Carcinogenicity | No data available |
| Germ cell mutagenicity | Test Type: Ames test Test system: Salmonella typhimurium Metabolic activation: with and without metabolic activation Method: OECD Test Guideline 471 Result: negative |
| Reproductive toxicity | No data available |
| Specific target organ toxicity -single exposure |
No data available
|
| Additional Information | Assessment : The substance/mixture does not contain components considered to have endocrine disrupting properties according to REACH Article 57(f) or Commission Delegated regulation (EU) 2017/2100 or Commission Regulation (EU) 2018/605 at levels of 0.1% or higher. Liver - Irregularities - Based on Human Evidence |
| Persistence and degradability | The methods for determining the biological degradability are not applicable to inorganic substances. |
| Toxicity to fish | No data available |
| Toxicity to daphnia and other aquatic invertebrates | No data available |
| Toxicity | No data available |
| Toxicity to bacteria | No data available |
| Toxicity to algae | No data available |
| Products Biodegradation | No data available |
| Mobility in soil | No data available |
| Results of PBT and vPvB assessment | This substance/mixture contains no components considered to be either persistent, bioaccumulative and toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher. |
| Endocrine disrupting properties | Assessment : The substance/mixture does not contain components considered to have endocrine disrupting properties according to REACH Article 57(f) or Commission Delegated regulation (EU) 2017/2100 or Commission Regulation (EU) 2018/605 at levels of 0.1% or higher. |
| Other adverse effects | Biological effects: Harmful effect due to pH shift. Hazard for drinking water supplies. Forms corrosive mixtures with water even if diluted. Discharge into the environment must be avoided. May be harmful to aquatic organisms due to the shift of the pH. |
| No data available |
| UN number | ADR/RID: 2032 IMDG: 2032 IATA: 2032 |
| UN proper shipping name | ADR/RID: NITRIC ACID, RED FUMING IMDG: NITRIC ACID, RED FUMING IATA: Nitric acid, red fuming Passenger Aircraft: Not permitted for transport Cargo Aircraft: Not permitted for transport |
| Transport hazard class(es) | ADR/RID: 8 (5.1, 6.1) IMDG: 8 (5.1, 6.1) IATA:8 (5.1, 6.1) |
| Packaging group | ADR/RID: I IMDG: I IATA:- |
| Environmental hazards | ADR/RID: no IMDG Marine pollutant: no IATA: no |
| Special precautions for user | Tunnel restriction code : (C/D) Further information : No data available |
| Further information | None |
| Safety, health and environmental regulations/legislation specific for the substance or mixture | This material safety data sheet complies with the requirements of Regulation (EC) No. 1907/2006. |
| Other regulations | Observe work restrictions regarding maternity protection in accordance to Dir 92/85/EEC or stricter national regulations where applicable. Take note of Dir 94/33/EC on the protection of young people at work. |
| Chemical Safety Assessment | A Chemical Safety Assessment has been carried out for this substance. |
| Other Information |
The information above is believed to be accurate and represents the best information currently available to us. However, we make no warranty of merchantability or any other warranty, express or implied, with respect to such information, and weassume no liability resulting from its use. Users should make their own investigations to determine the suitability of the information for their particular purposes. In no event shall be liable for any claims, losses, or damages of any third party or for lost profits or any special, indirect, incidental, consequential or exemplary damages, howsoever arising, even if Rx Marine International has been advised of the possibility of such damages. |
Availability
NITRIC ACID manufacturer supplier distributor in Mumbai, Kandla, Kolkata, Vizag, Chennai, India, Fujairah, Dubai UAE, Muscat Oman, Kenya Africa. Get the best quality of NITRIC ACID at a competitive price from us. We have ready stock of NITRIC ACID in India, UAE Gulf, Oman, Kenya Africa. Contact us for bulk as well as small orders.