PROEDURE OF USE:-

1st Method:-
Mix 1 part of RXSOL-10-1005-025 with 2 -10 parts of water / GAS-OIL  , For heavy oil,greasy surface use directly)Spray directly on the entire surface to be cleaned. This can be achieved by Hand spray / mechanical spray pump. Immediately after 2 -5 minute of spray the RXSOL-10-1005-025 starts its function. The Dirt, oil grease etc will loosen. 5 to 6 minutes after spraying start rinsing the system with water (High pressure recommended). Dirt and mud starts vanishing with cleaning media and water.

2nd Method:-
Application in immersion process with or without ultrasonic support, manual wipping.

3rd Method:- 
RXSOL-10-1005-025 is also used in conjunction with alkaline degreasing bath at 3-5% (v/v) concentration for better and quick degreasing action. Eithers the bath is heated to be 70c or the solution can be stirred or air agitated.

Key Features of Degreaser Heavy Duty

• Superior Cleaning Power – Quickly dissolves and removes heavy oil, grease, wax, carbon deposits, and tough hydrocarbon residues.
• Water Soluble in All Proportions – Easily mixes with water, allowing flexible dilution for light to heavy-duty cleaning.
• Dual Action (Solvent + Detergent) – Solvent base penetrates and loosens stubborn residues, while surfactants disperse and emulsify them for easy rinsing.
• Non-Corrosive – Safe on common metals such as mild steel, copper, aluminium, and also compatible with plastics.
• Reduced Manual Effort – Cuts through thick grease layers without excessive scrubbing, saving time and labor.
• Versatile Application – Suitable for spray, brush, soak, or circulation cleaning systems in marine, industrial, automotive, and workshop environments.
• Residue-Free Rinsing – Emulsifies contaminants and rinses away cleanly, leaving surfaces oil-free and ready for use.
• Safe to Handle – Non-toxic formulation ensures safer handling compared to harsh solvent-only degreasers.
• Economical – Concentrated formula offers high coverage area and low consumption per cleaning cycle.

Mechanism: It converts calcium hardness into soft, non-adherent sludge that is easily removed by blowdown.

The presence of alkalinity in a water sample may be due to many different substances.  However, for the sake of simplicity, the presence of bicarbonate, carbonate, and hydroxide ions is commonly considered as alkalinity.  The points of change in colour of phenolphthalein and methyl orange indicators, which occur at pH 8.3 and pH 4.3 provide standard reference points which are almost universally used to express alkalinity.

Very high alkalinity values can be undesirable in an industrial water supply.  For example, the presence of a high methyl orange alkalinity should be avoided in boiler feed water because of the resultant carbon dioxide content of the steam.  Carbon dioxide usually is responsible for the corrosion of steam and return lines.  High boiler water alkalinities are also undesirable because the presence of high hydroxide ion concentration is the primary cause of caustic metal embrittlement. A very high boiler alkalinity can also lead to an undesirable carryover condition.  On the other hand, the alkalinity of boiler water must be sufficiently high to protect the boiler metal against acidic corrosion and to ensure precipitation of scale-forming salts.  Usual treatment approaches include setting both a minimum alkalinity level and an operating range.
 

Hydroxide alkalinity may be determined by adding barium chloride prior to titration to precipitate the carbonate ion from solution, allowing direct titration of the hydroxide alkalinity.  Measurement of hydroxide alkalinity is also used to control lime soda softeners.
 

In cooling water systems, alkalinity is of major importance since the total alkalinity of a water is one factor that must be considered when predicting the tendency for the water to precipitate calcium carbonate scale.  Depending on the choice of chemical treatments to protect against corrosion and scale formation, the operating alkalinity and pH ranges are chosen to balance these two features.

Alkalinity Titrimetric Method (0-200 ppm) 

Principle Theory

This test is based on the determination of alkalinity by titration with standard acid to the phenolphthalein colour change (or to a pH of 8.3) and to the methyl orange colour change (or a pH of 4.3).  For determination of hydroxide alkalinity only, barium chloride is added prior to titration to precipitate the carbonate ions.  Titration is then taken only to the phenolphthalein endpoint.  A pH meter may be used instead of the indicators to determine the endpoints of the titration.