餐具洗涤剂配方的研制

采用复配技术制取餐具洗涤剂。对产品外观、pH值、稳定性、去污力进行了分析。通过正交实验,利用阴离子和非离子2种表面活性剂与各种助剂复配制得高性能、低成本的餐具洗涤剂。     

Optimization of an Alkylpolyglucoside-Based Dishwashing Detergent Formulation

The aim of this work was to formulate and optimize the washing performance of an alkylpolyglucoside-based dishwashing detergent. The liquid detergent was formulated with five ingredients of commercial origin: anionic (linear sodium alkylbenzenesulfonate and sodium laurylethersulfate), nonionic (C₁₂–C₁₄ alkylpolyglucoside) and zwitterionic (a fatty acid amide derivative with a betaine structure) surfactants, and NaCl for viscosity control. In addition to the plate test, other properties were investigated including “cloud point”, viscosity, and emulsion stability. Statistical analysis software was used to generate a central composite experimental design. Then, a second order design and analysis of experiments approach, known as the Response Surface Methodology, was set up to investigate the effects of the five components of the formulation on the studied properties in the region covering plausible component ranges. The method proved to be efficient for locating the domains of concentrations where the desired properties were met.

Development of an Environmentally Acceptable Detergent Formulation for Fatty Soils Based on the Lipase from the Indigenous Extremophile Pseudomonas aeruginosa Strain

A lipase derived from an indigenous extremophile Pseudomonas aeruginosa strain isolated from rancid metalworking fluid was evaluated as a detergent additive. Applicability of the obtained enzyme as an additive in detergent formulations was confirmed by its implementation in the formulations of several new products differing in surfactant type and concentrations, demonstrating satisfactory performance in terms of degreasing efficiency and composition of the washing wastewater. The degreasing efficiency of different enzyme‐containing detergent formulations was studied on cotton fabric samples stained with triolein and compared to that of formulations containing only surfactant. The highest efficiency of the fatty soil removal in formulations with a low content of surfactants (0.4 %) was noted in the enzyme formulation containing Lutensol^® XP‐80 (degreasing efficiency >80 %) and Triton^® X‐100 (degreasing efficiency >60 %). An attempt was then made to optimize the composition of the enzyme formulation on the basis of one or both of these surfactants using statistically planned experiments and response surface methodology (RSM). Taking into consideration the environmental aspects and the shown detergency, it appeared that rather high degreasing effects were achieved in formulations based on a low quantities of Lutensol^® XP‐80 (0.4 %) at all pH values. However, pH seemed to have a notable effect since the degreasing efficiency significantly increased with increasing pH and the amount of the enzyme. Formulations having a moderate alkaline pH profile and higher amount of enzyme exhibited a high cleaning performance of fatty soil even at a low concentration of the surfactant.     

Purification of Bacillus licheniformis Lipase and its Application as an Additive in Detergent for Destaining

In this study, we aimed to optimize the nutritional and environmental conditions for the production of a novel lipase (LBL) from Bacillus licheniformis (GenBank accession no. MT118724). This strain was characterized by morphological and biochemical assays and Sanger sequencing of 16S rDNA. The crude lipolytic activity reached a maximum level 7.5 U mL⁻¹ at 40 °C and pH 8.0 using olive oil as substrate. Additionally, the crude enzyme maintained 100% of its initial activity after incubation for 1 h at 50 °C and pH 9.0. It is mandatory to note that LBL lipase displayed appreciable stability over a wide pH range and extreme temperatures. After purification, the optimal lipolytic activity was observed at pH 8.0 and 40 °C. LBL was shown to be a monomeric protein with an estimated molecular weight of 40 kDa. This novel lipase exhibited high stability and excellent compatibility compared to lipase extracted from Thermomyces lanuginosa (Lipolase® from Novozymes, Denmark) toward various detergents. Washing performance analysis revealed that it efficiently removes tomato sauce stain from cotton cloth. All these interesting enzymatic properties favor this new lipase as a potent candidate for applications in detergent formulations.     

Burkholderia multivorans SB6 Lipase as a Detergent Ingredient: Characterization and Stabilization

In this study, 265 bacterial isolates were collected from kitchen wastewater samples using Rhodamine B agar medium. Of these, 115 isolates were found to respond positively to the addition of commercial detergents. Using 16S rRNA sequence analysis, the isolate demonstrating the high stability towards commercial detergents was identified as Burkholderia multivorans. An SB6 lipase with a molecular mass of 70 kDa was purified from B. multivorans. The purified enzyme showed optimal activity at pH 9.0 and 40 °C and remained stable in the presence of various metal ions, surfactants, and oxidizing agents. The addition of boron compounds improved the pH stability and thermostability of the enzyme, which displayed stability against some commercial detergents; moreover, this stability increased when boron compounds were added to the incubation medium as stabilizers. These properties make SB6 lipase an ideal choice as an additive in detergent formulations.     

Application of Lipase from Marine Bacteria Bacillus sonorensis as an Additive in Detergent Formulation

The efficacy of lipase (triacylglycerol acylhydrolases EC 3.1.1.3) as a detergent additive from a newly isolated marine halophilic bacteria Bacillus sonorensis from marine clams Paphia malabarica collected in the Kalbadevi Estuary, Mumbai, has been assessed and reported. In terms of activity and stability, the lipase exhibited maximum activity in alkaline conditions and was observed to be stable over a temperature range from room temperature to 60 °C. The activity of the lipase increased in the presence of surfactants and detergents. Due to these properties of the lipase from marine bacteria, it was used as an additive in detergents to study its efficiency at corn oil removal from fabrics. The washing studies indicated that the efficiency of corn oil removal from the cotton fabrics increased by 20 % when lipase was incorporated in the detergent as compared to the treatment with detergent alone. The lipase was also capable of removing corn oil from natural as well as synthetic fabrics dyed with a respective, preferred class of dyes.     

Correlation Between Enzyme Activity and Stability of a Protease, an Alpha-Amylase and a Lipase in a Simplified Liquid Laundry Detergent System, Determined by Differential Scanning Calorimetry

Enzymes used during washing in laundry detergents have become a universal tool to lower energy consumption and to generate a broad, consumer-relevant, cleaning effect. However, the stability of these enzymes remains a major obstacle, particularly in liquid products, due to increased interaction between the enzymes and the other components of the detergent. The process of formulation involves extensive shelf-life stability studies where residual enzyme activities are correlated with formulation variations. As a way to improve the formulation process, we evaluated the possible use of differential scanning calorimetry (DSC) as a tool to predict enzyme stability in liquid detergents. Thus, residual enzyme activity after incubation in a multitude of formulations was determined and compared to thermodynamic data obtained by DSC. The enzymes tested were a protease, an alpha-amylase and a lipase. We found a strong linear correlation between DSC-derived data, in particular T _max (temperature at peak maximum of the transition from the folded to unfolded state) and enzyme activity studies with R ²-values: 0.98 (protease), 0.99 (amylase) and 0.98 (lipase), respectively. Thus, a higher T _max for the same enzyme in a particular formulation is directly proportional to longer storage stability. These results suggest a new way of greatly accelerating this type of formulation study, allowing estimation of enzyme compatibility with a specific formulation on a daily, rather than the weekly or monthly basis used at present.     

The Use of Boron Compounds for Stabilization of Lipase from Pseudomonas aeruginosa ES3 for the Detergent Industry

This study aimed to characterize a lipase that is highly active and stable under typical washing conditions for use as a detergent ingredient by investigating the effects of various boron compounds on lipase stabilization under different conditions. In addition, the antimicrobial activity of the boron compounds used in enzyme stabilization was examined in order to obtain an effective antimicrobial detergent. A lipase‐producing bacterium was isolated from kitchen wastewater samples using Rhodamine‐B Agar medium and identified as Pseudomonas aeruginosa based on 16S rDNA sequence analysis. The ES3 lipase obtained from P. aeruginosa was purified, and the purified enzyme was found to have a molecular mass of 40 kDa. The enzyme showed optimal activity at pH 9.0–10.0 and 40 °C and remained stable in the presence of various metal ions, surfactants and oxidizing agents. Moreover, the pH stability and thermostability of the enzyme was improved by the addition of boron compounds, which, when used as stabilizers in the incubation media, also increased the stability of the enzyme towards commercial detergents. Furthermore, the enzyme displayed properties comparable with the commercial product Lipolase^®, which has shown excellent stability towards various commercial detergents. Finally, boron compounds used to stabilize the lipase were found to possess antimicrobial properties, suggesting that detergents incorporating these compounds will also exhibit antimicrobial activity when washing clothes and dishes.     

Rapid and Simple Identification and Quantification of Components in Detergent Formulations by Nuclear Magnetic Resonance Spectroscopy

A rapid, inexpensive, and simple high-resolution NMR spectroscopic method is outlined for determining the content of surfactants and other low-molecular-weight organic compounds in detergent formulations. With simple sample preparation, quantitative results can be obtained from an internal standard and/or the method can be used as a fingerprint analysis of the surfactant composition. The NMR sample is prepared by suspending the detergent sample in deuterated acetic acid and thus dissolving surfactants and other organic compounds. Any content of carbonate will be liberated as CO₂, whereas other inorganic materials are removed by centrifugation. From one-dimensional ¹H and two-dimensional HSQC NMR spectra, the surfactant components and low-molecular-weight organic compounds can be identified from reference spectra. Intensities of signature signals in the one-dimensional ¹H NMR spectrum are used for quantification by comparing with an internal standard. Furthermore, it is demonstrated how ³¹P NMR can be used to identify and quantify phosphonate-type chelators.     

Drawbacks of Surfactant Presence on the Dissolution and Mechanical Properties of Detergent Tablets: How to Control Interfaces by Surfactant Localization

The aim of this study is to limit the hurdles generated by the presence of a surfactant, i.e., sodium dodecyl sulfate (SDS), in effervescent detergent tablets containing a chlorine provider. The results are highlighted by investigating the tablet’s functional characteristics (mechanical strength, disintegration time). A second objective is to increase the surfactant content of the tablet in order to improve the cleaning properties of the detergent formula without retaining the previous drawbacks. For low tablet porosity, mechanical properties are damaged by the presence of 2% of SDS and while disintegration through an erosion mechanism is slowed down. Experimental evidence indicated that these phenomena are associated with the coexistence of SDS and sodium dichloroisocyanurate (DCCNa). Their separation by locating SDS in the tablet core was encouraging but had limited value due to the slow dissolution of the SDS core. The problem was solved when 2% SDS was concentrated on one face of the tablet; however, a higher concentration induced a delayed disintegration due to the progressive erosion of SDS, which behaved as a massive solid. The coating of the tablet with SDS was beneficial because the dissolution of the film delayed effervescence and consequently disintegration. Neither coating the SDS particles with cellulosic film nor including them in zeolite was an appropriate solution. On the other hand, segregating SDS and DCCNa by placing them in separate layers of the tablet produced very conclusive results when microcrystalline cellulose and an effervescent system were added to the SDS. Furthermore, this bilayer tablet allowed the SDS content to be increased while a satisfactory tensile strength and a low disintegration time were retained.

Evaluating the Performance of Detergent Powder Formulations Containing Nano Alumina Using Diffuse Reflectance Infrared Spectroscopy and Pattern Recognition Techniques

An analytical method has been introduced based on diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) coupled with pattern recognition techniques to determine the efficiency of various detergent powder formulations containing nano alumina. In order to reach this aim, different multivariate classification methods such as principal component analysis, hierarchical cluster analysis and linear discriminate analysis (LDA) were utilized for diffuse reflectance spectra to evaluate the classification approach. The best model was predicted by LDA, with a correct classification rate (%CC) of 93.55 %. Furthermore, sensitivity and specificity for the test set were 0.90 and 0.95, respectively. These results confirm the capability of DRIFTS coupled with chemometric techniques for estimating the performance of detergent powder formulations containing nano alumina.     

Purification and Characterization of a Lipase with High Thermostability and Polar Organic Solvent‐Tolerance from Aspergillus niger AN0512

An extracellular lipase (EC 3.1.1.3, AN0512Lip) from Aspergillus niger AN0512 was purified and its characteristics were investigated. After the process of ammonium sulfate precipitation followed by ion‐exchange chromatography and gel filtration, the purified lipase was achieved with 203.6‐fold purification and 22.1 % recovery. AN0512Lip exhibited the highest activity at 50 °C and pH 5.0. It was thermostable and pH‐stable, as indicated by that more than 50 % activity retained at 60 °C for 20 h and more than 90 % activity retained at pH 3.0 for 20 h, respectively. AN0512Lip activity was stimulated by some divalent metal ions (especially Cu²⁺, Ca²⁺), while greatly suppressed by EDTA, indicating that AN0512Lip was a metal‐activated enzyme. Moreover, AN0512Lip exhibited high tolerance for various polar organic solvents with log P < 0.8, and the highest lipase activity (476 % of its original activity) was achieved after addition of 90 % (V/V) isopropanol to the reaction mixture. AN0512Lip also displayed 3‐regiospecificity and great affinity for the long‐chain fatty ester. The preliminary test showed that AN0512Lip was a candidate for enriching EPA and DHA in fish oil. All the unique properties, such as thermostability, Cu²⁺‐dependent, 3‐regiospecificity, and polar organic solvent‐tolerance, indicated that AN0512Lip could have potential applications in the food industry, even in organic synthesis and the pharmaceutical industry.     

Preparation of Environmentally Friendly Amino Acid‐Based Anionic Surfactants and Characterization of Their Interfacial Properties for Detergent Products Formulation

In this study, 2 types of amino acid‐based biosurfactants such as potassium cocoyl glycinate (CGK) and sodium cocoyl glycinate (CGN) were synthesized from coconut oil. Their chemical structures were identified using FT‐IR, ¹H NMR, and ¹³C NMR spectroscopies. Characterization of their interfacial properties has shown that both CGK and CGN surfactants are surface‐active and effective in reducing interfacial free energy. Washing test results indicated relatively good detergency compared with surfactants commonly employed in detergent applications. From environmental compatibility tests, both CGK and CGN are found to be readily biodegradable, nontoxic, nonirritating, and very mild. In particular, the CGK surfactant was found to be more efficient in reducing interfacial free energy since a larger number of CGK molecules are preferentially adsorbed at the air–water interface due to higher hydrophobicity and larger mobility of CGK than CGN, indicating possible uses in detergent applications.     

Production and Characteristics of an Enantioselective Lipase from Burkholderia sp. GXU56

The lipase production of Burkholderia sp. GXU56 was influenced by carbon and nitrogen sources, inorganic salts, initial pH of the medium and cultivation temperature. The maximum lipase production was 580.52 U/mL and reached 5 times the level of the basic medium in the optimum medium at pH 8.0, 32 °C, 200 rpm and 40–48 h. The lipase was purified 53.6 fold to homogeneity and the molecular weight was 35 KDa on SDS‐PAGE. The optimum pH and temperature of the lipase were 8.0 and 40 °C, respectively, and it was stable in the range of pH 7–8.5 and at temperatures below 45 °C. The lipase activity was strongly inhibited by Zn²⁺, Cu²⁺, Co²⁺, Fe²⁺, Fe³⁺ ions and SDS, while it was stimulated by Li⁺ and Ca²⁺ ions and in presence of 0.1 % CTAB, 0.1 % Triton X‐100 and 10 % DMSO. K_m and V_max of the lipase were calculated to be 0.038 mmol/L, and 0.029 mmol/L min^–1, respectively, with PNPB as the substrate. The GXU56 lipase showed enantioselective hydrolysis of (R,S)‐methyl mandelate to (R)‐mandelic acid, which is an important intermediate in the pharmaceutical industry.     

Ionic Liquids Increase the Catalytic Efficiency of a Lipase (Lip1) From an Antarctic Thermophilic Bacterium

Lipases catalyze the hydrolysis and synthesis of triglycerides and their reactions are widely used in industry. The use of ionic liquids has been explored in order to improve their catalytic properties. However, the effect of these compounds on kinetic parameters of lipases has been poorly understood. A study of the kinetic parameters of Lip1, the most thermostable lipase from the supernatant of the strain ID17, a thermophilic bacterium isolated from Deception Island, Antarctica, and a member of the genus Geobacillus is presented. Kinetic parameters of Lip1 were modulated by the use of ionic liquids BmimPF6 and BmimBF4. The maximum reaction rate of Lip1 was improved in the presence of both salts. The highest effect was observed when BmimPF6 was added in the reaction mix, resulting in a higher hydrolytic activity and in a modulation of the catalytic efficiency of the enzyme. However, the catalytic efficiency did not change in the presence of BmimBF4. The increase of the reaction rates of Lip1 promoted by these ionic liquids could be related to possible changes in the Lip1 structure. This effect was measured by quenching of tryptophan fluorescence of the enzyme, when it was incubated with each liquid salt. In conclusion, the hydrolytic activity of Lip1 is modulated by the ionic liquids BmimBF4 and BmimPF6, improving the reaction rate and the catalytic efficiency of this enzyme when BmimPF6 was used. This effect is probably due to changes in the structure of Lip1 induced by the presence of these ionic liquids, stimulating its catalytic activity.     

Isolation and Evaluation of Stearin and Olein Fractions from Rice Bran Oil Fatty Acid Distillate by Detergent Fractionation and Conversion into Neutral Glycerides by Autocatalytic Esterification Reaction

Detergent fractionation (Lanza process) offers a valuable separation process for edible oils that contain varying amounts of saturated and unsaturated fatty acids. The rice bran oil fatty acid distillate (RBOFAD), obtained as a major byproduct of rice bran oil deacidification refining process, was fractionated by detergent solution into a fatty acid mixture as follows: low-melting (19.00 °C) fraction of fatty acids as olein fraction (44.50 g/100 g) and high-melting (49.00 °C) fatty acids as stearin fraction (37.15 g/100 g). A high amount of palmitic acid (42.75 wt%) is present in stearin fraction, while oleic acid is higher (48.21 wt%) in the olein fraction. The stearin and olein fractions of RBOFAD with very high content of free fatty acids are converted into neutral glycerides by autocatalytic esterification reaction with a theoretical amount of glycerol at high temperatures (130–230 °C) and at a reduced pressure (30 mmHg). Acid value, peroxide value, saponification value, and unsaponifiable matters are important analytical parameters to identity for quality assurance. These neutral glyceride-rich stearin and olein fractions, along with unsaponifiable matters, can be used as nutritionally and functionally superior quality food ingredients in margarine and in baked goods as shortenings.     

Optimization of a Fabric Softener Formulation with an Electrochemical Sensor and Streaming Potential Measurements

An electrochemical, cationic, surfactant-selective sensor based on multiwalled carbon nanotubes (MWCNT) functionalized with a sulfate group and the cetylpyridinium ion (MWCNT–OSO₃⁻CP⁺) as a sensing material was used for optimization of the formulation of a fabric softener. Potentiometric titrations were performed and response measurements were obtained using four cationic surfactants (CS) of technical grade and four CS of analytical grade. The slope closest to Nernstian was obtained for di-(tallow carboxyethyl) hydroxyethyl methylammonium methosulfate (MAS) (59.5 ± 1.1 mV/decade of activity in water and 57.5 ± 1.3 mV/decade of activity in CaCl₂). When using CS as analytes in potentiometric titrations, the best accuracy (99.8%) was obtained when using MAS; therefore, it was chosen as the CS for the fabric softener formulation. Due to the better properties of fabric softeners with silicone in their formulations, four silicones at several concentration levels were used as potential additives. Based on the stability and viscosity of the system, the diquaternary polydimethylsiloxane (DPS) (w = 0.19%) was chosen for the fabric softener formulation. The pH did not significantly influence the potential when in the range of 3–8 or the recovery of potentiometric titrations when in the range of 3–7. The application profile of the CS was assessed through streaming potential measurements of reference fabrics in an electrokinetic analyzer. The obtained electrokinetic parameters indicated on lag in adsorption of model fabric softener (MFS) based on MAS (w = 9%), with the addition of silicone DPS (MFS 3), on cotton and polyester fabrics, but advantage in stability when compared with other MFS investigated.     

Improvement of Thermal Stability via Outer-Loop Ion Pair Interaction of Mutated T1 Lipase from Geobacillus zalihae Strain T1

Mutant D311E and K344R were constructed using site-directed mutagenesis to introduce an additional ion pair at the inter-loop and the intra-loop, respectively, to determine the effect of ion pairs on the stability of T1 lipase isolated from Geobacillus zalihae. A series of purification steps was applied, and the pure lipases of T1, D311E and K344R were obtained. The wild-type and mutant lipases were analyzed using circular dichroism. The T_m for T1 lipase, D311E lipase and K344R lipase were approximately 68.52 °C, 70.59 °C and 68.54 °C, respectively. Mutation at D311 increases the stability of T1 lipase and exhibited higher T_m as compared to the wild-type and K344R. Based on the above, D311E lipase was chosen for further study. D311E lipase was successfully crystallized using the sitting drop vapor diffusion method. The crystal was diffracted at 2.1 Å using an in-house X-ray beam and belonged to the monoclinic space group C2 with the unit cell parameters a = 117.32 Å, b = 81.16 Å and c = 100.14 Å. Structural analysis showed the existence of an additional ion pair around E311 in the structure of D311E. The additional ion pair in D311E may regulate the stability of this mutant lipase at high temperatures as predicted in silico and spectroscopically.     

一种经济型清洁压裂液配方研究与性能评价

粘弹性表面活性剂(Viscoelastic surfactant,下文简称VES)压裂液与传统聚合物压裂液不同,可消除残余聚合物对支撑剂充填层的堵塞,并能有效提高导流能力,减少对地层的损害及污染,压后油气产量比使用传统压裂液有显著提高。介绍了VES压裂液的原理及配方设计原则。通过室内试验确定了一种经济型VES压裂液的配方,并对其性能进行了相关评价。     

Pharmacological Evaluation and Preparation of Nonsteroidal Anti-Inflammatory Drugs Containing an N-Acyl Hydrazone Subunit

A series of anti-inflammatory derivatives containing an N-acyl hydrazone subunit (4a–e) were synthesized and characterized. Docking studies were performed that suggest that compounds 4a–e bind to cyclooxygenase (COX)-1 and COX-2 isoforms, but with higher affinity for COX-2. The compounds display similar anti-inflammatory activities in vivo, although compound 4c is the most effective compound for inhibiting rat paw edema, with a reduction in the extent of inflammation of 35.9% and 52.8% at 2 and 4 h, respectively. The anti-inflammatory activity of N-acyl hydrazone derivatives was inferior to their respective parent drugs, except for compound 4c after 5 h. Ulcerogenic studies revealed that compounds 4a–e are less gastrotoxic than the respective parent drug. Compounds 4b–e demonstrated mucosal damage comparable to celecoxib. The in vivo analgesic activities of the compounds are higher than the respective parent drug for compounds 4a–b and 4d–e. Compound 4a was more active than dipyrone in reducing acetic-acid-induced abdominal constrictions. Our results indicate that compounds 4a–e are anti-inflammatory and analgesic compounds with reduced gastrotoxicity compared to their respective parent non-steroidal anti-inflammatory drugs.