Aqueous Zwitterionic Hydrotrope Composition for Surfactant Wetting
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Solution Overview
Problem
Existing nonionic surfactants in cleaning compositions face solubility issues in aqueous solutions with high electrolyte content, and conventional hydrotropes do not effectively enhance wetting ability.
Innovation Solution
An aqueous composition containing a specific hydrotrope with a C6-C22 alkyl group and a zwitterionic structure is used, enhancing the solubility and wetting ability of nonionic surfactants.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Quantity of substance
If conventional hydrotropes are used to improve solubility of nonionic surfactants, then solubility is enhanced, but wetting ability is not effectively improved
Solution Approach 1:
The patent modifies the chemical structure of conventional hydrotropes by introducing a zwitterionic group to the aromatic ring. This structural parameter change enables the molecule to simultaneously provide solubility enhancement (through its hydrotropic properties) and wetting ability (through its zwitterionic character), resolving the contradiction between improving solubility while maintaining wetting performance
Solution Approach 2:
The invention creates a composite molecular structure that combines the hydrophobic aromatic core (providing hydrotropic solubility enhancement) with a zwitterionic functional group (providing wetting ability). This molecular-level composite allows a single compound to fulfill both functions that were previously separated, eliminating the trade-off between solubility and wetting performance
2Ease of operation
If nonionic surfactants are used as wetting agents in cleaning compositions, then wetting ability is provided, but solubility is insufficient in high electrolyte content solutions
Solution Approach 1:
The patent changes the chemical parameters of the surfactant system by incorporating a zwitterionic hydrotrope with specific structural features (aromatic core with zwitterionic group). This parameter change allows the system to maintain wetting ability while achieving sufficient solubility in high electrolyte content cleaning compositions, directly resolving the solubility limitation of conventional nonionic surfactants
3Productivity
If alkali hydroxides and alkaline builders are added to cleaning compositions, then cleaning performance is improved, but solubility of nonionic surfactants decreases
Solution Approach 1:
The zwitterionic hydrotrope acts as an intermediary substance that bridges the incompatibility between alkaline cleaning agents and nonionic surfactants. Its unique zwitterionic structure allows it to function as a solubility enhancer in high-alkaline environments, enabling the coexistence of alkali hydroxides/builders (for cleaning performance) and nonionic surfactants (for wetting and cleaning action) in the same composition
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
The composition demonstrates improved cleaning performance on hard surfaces by ensuring even spreading and solubility of nonionic surfactants, outperforming conventional formulations.
Implementation Method 1
The primary task of a hydrotrope is to enhance the solubility of the nonionic surfactant
Implementation Method 2
Nonionic surfactants are known to be wetting agents
Implementation Method 3
The ability of an aqueous solution to spread evenly over a surface, i.e., a wetting ability, is desirable for many applications
Data Source
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AI summary
ABSTRACT OF THE DISCLOSURE An aqueous composition includes water, a surfactant; and a hydrotrope present in an amount of at least 0.5 weight percent actives based on a total weight of the composition. The hydrotrope has the structure: wherein R is a C6 - C22 alkyl group, each of R1 and R2 is independently a C1 - C4 alkyl group; n is a number of from about 8 to about 25. X- is a zwitterion having the structure: wherein each of R4 and R5 is independently H, CH3, or (CH2)2COOY, wherein Y is H, Na, or K; and wherein R6 is H, CH3, CH2COOY, CH2CH2COOY, or (CH2)2N(CH2COOY)CH2COOY.