Using Thin Layer Chromatography To Monitor Reactions Environmental Sciences Essay

Using Thin Layer Chromatography To Monitor Reactions environmental Sciences EssayThin floor chromatography (tender loving c atomic number 18) is a in truth useful technique for monitoring reactions. It tin can as well be utilise to determine the fit firmness of purpose system for performing separations employ newspaper column chromatography. tender loving care stationary phases argon usu every last(predicate)y alumina or silicon oxide. They argon polar for regulation proves or non-polar for reverse phase chromatography. The mobile phase is a picture whose polarity is chosen by the person conducting the experiment. In closely science laboratory work standard phase silica plates are used. Different compounds forget jaunt distinguishable distances up the plate de compileding on the polarity of the dowrys of the mixture. The more polar compounds will be more attracted to the polar silica mousse and travel shorter distances on the plate. Mon-polar substances will s compiled more period in the mobile phase and as a head will travel larger distances on the plate. The measure of the distance a compound travels is called the store factor (Rf ) value.The retention factor, or Rf, is defined as the distance traveled by the compound divided by the distance traveled by the final result.For example, if a compound travels 2.1 cm and the consequence front travels 2.8 cm, the Rf is 0.75The Rf for a compound is a constant from one experiment to the adjoining only if the chromatography conditions below are similarly constantsolvent system adsorptivethickness of the adsorbentamount of material faulttedtemperatureSince these factors are difficult to keep constant from experiment to experiment, relative Rf value are generally considered. Relative Rf means that the values are reported relative to a standard, or it means that you compare the Rf values of compounds run on the selfsame(prenominal) plate at the same succession.1.1 Thin Layer Chromatog raphyThere put up been a numbered of primary(prenominal) milestones in the evolution of chromatography in the last 100 years. Each of these milestones has signalled the start of an important branch of chromatography. Some examples of these are partition chromatography (1941), gas chromatography (1951-1952), high implementation fluent chromatography (mid- 1960s), capillary electrophoresis (1980) and capillary electrochromatography (past decade).In all the chromatographic techniques mentioned, separation is carried out in a column. However, it is also possible to declare out separations on a planar surface. Two examples of this are base chromatography (1944) and thin-layer chromatography (1937-1938). Thin-layer chromatography (tender loving care) replaced paper chromatography as the most popular, routine chromatographic technique.tender loving care was number 1 used in 1937 to 1938 by Nikolai A. Izmailov and Maria S. Shraiber at the Institute of observational Pharmacy of the S tate University of Kharkov. At the time Izmailov was the head of the institute and Shraiber was his polish student. They were searching for a system acting for the rapid analytic th signing of galenic pharmaceutical preparations (plant extracts). As classical column chromatography would have taken too much time they felt that if the absorbent would be prepared in the form of a thin-layer on a glassful plate. They believed that it would behave like a column but the characterization time would be much shorter. They coated microscope slides with a sus create verballysion of variant adsorbents (calcium, magnesium and aluminium oxides). They deposited one drop of the smack solution on this layer and added one drop of the same solvent used in a column to mature separation. The test was a success as the illogical take in components appeared as concentric peal that fluoresced in variant polishs under a UV lamp. They showed that the place of the concentric multicoloured rings on the plate would have been like to the sequence of coloured rings obtained on a normal chromatographic column. They called this technique location chromatography and the result on the microscope slides ultrachromatograms.The paper on this experiment was promulgated in a Russian pharmaceutical journal that was much un cognize outside the then Soviet Union. Its abstract was included in a Russian review journal and through with(predicate) it in chemic Abstracts. It was then read by M. OL. Crowe of the New York State Department of Health. He then adapted the technique for his own use. Crowe prepared the adsorbent layer in a Petri dish, added a drop of the sample solution in the centre and then added the developing solvent dropwise until fitted separation was obtained.In 1947 T.I. Williams described a further improvement of the method of Izmailov and Shraiber in his textbook on chromatography. He prepared the adsorbent-coated glass plates in the form of a sandwich. The adsorbent la yer was covered by 2 glass plates and had a small hole which the sample drops could be applied through.Meinhard and Hall do the next major step in the development of tender loving care at the University of Wisconsin. They used corn starch, which acted as a binder, to hold the coating on the glass plate and added a small amount of Celite powder to the adsorbent particles to improve the consistency of the layer. They called this surface chromatography. They used it to sepa regularize inorganic ions. new tender loving care started 50 years ago with the work Department of agriculture Fruit and Vegetable laboratory in Southern California. He investigated the scag components of the juices of citrus fruits. However, he stated that very large volumes had to be treat because the amount of flavour material was extremely small. A nonher problem was in finding an analytical method for the investigation of the juice concentrate composition.He followed the method of Meinhard and Hall that he read in Chemical Abstracts. However, kind of of adding just a drop of the developing solvent he unquestionable the plates as in paper chromatography. The plates were developed in a closed(a) chamber and one side was dipped into the solvent. The solvent then ascended through the plate by capillary action. It carried with it the sample components and they were uninvolved as a result. The experiments carried out were published and are considered the start of modern TLC.Egon Stahl was responsible for TLC becoming a universally accepted technique. He was also the premiere to use the term thin-layer chromatography to characterize the technique. This choice of represent was almost direct accepted.Stahl investigated motley essential oils and obtained good results victimization adsorbent-coated glass plates. However, neither the method nor the adsorbent to be used had been optimized. Also, the adsorbents had to be modified and treated ahead they could be used for the coating of plat es. Stahl started investigating the operational parameters and the adsorbent preparations. In the spring of 1958 his efforts were fulfilled as the necessary basic instrumentation, make by Desaga and silica gel G match to Stahl for TLC, made by E. Merck were twain introduced at the international Achema exhibition of chemical equipment in Frankfurt. Stahl also published an article outlining the use of the system and a wide range of screenings. Because of this convertible method TLC became a widely used laboratory technique. He also went on to publish a TLC handbook in 1962.Although TLC had a wide natural covering it was still thought to be a qualitative technique for the analysis of ingenuous mixtures. As a result advances were directed toward improving the technique. Instrumentation which permitted more precise detective work of the sample onto the plates and the quantitative evaluation of the separated spots was developed. Faster analysis and higher separation power was also achieved. As a result of the higher performance ability the name was change to high-performance TLC (HPTLC) by R.E. Kaiser, who was instrumental in its development.The particle size and range of the adsorbent was the main difference mingled with TLC and HPTLC. The silica gel for TLC had broad particle sizes of 10-60m with an fair of 20m whereas HPTLC has an average of only 5m. the HPTLC plates were also smaller in comparison with TLC plates, 10 x 10cm and 20 x 20cm seeively. The im prove method and excogitation allowed reduction in the diameter of the starting spots. These improvements lowered the analysis time and increased the efficiency. Problems arose with flow rate which Kaiser overcame by applying pressure to the TLC plate. This in turn led to forced-flow TLC.Due to the constant condensation-evaporation process associated with developing TLC plates in developing domiciliate problems can be encountered because of the changing upper of the mobile phase. To overcome this fo rced-flow TLC (FFTLC) was developed by Tyihk, Mincsovics and Kalsz. In this method the spotted plates (dry) are placed into a pressurized development chamber. The stationary-phase layer is tightly covered and sealed on its side by an elastic tissue layer and pressurized by an inert gas or water filling up the cushion above the layer. The mobile phase is delivered via a pump at a constant velocity through a slit in the membrane to the stationary phase. There are various configurations which can be handled utilise this method.TLC is a very simple technique. As a result very little instrumentation is essential. Application of samples to the stationary-phase is carried out using a micropipette or syringe. The developing chambers are simple glass structures. Detection is carried out by visual inspection or made visible by spraying the plate with reagent. Also, a wide sort of precoated plates are available so coating equipment isnt needed.In more go on systems the samples may be spot ted by automated loading devices (dosimeters). This allows the application of small and uniform sample spots. More sophisticated developing chambers are also available (FFTLC). The plates can be scanned by densitometers and quantitatively analysed using absorbance or fluorescence measurements. Chromatograms with peaks of the individual separated spots recorded against the distance of the plate are produced with such(prenominal) analyses. Their area is also a likeness to the amount present. More complex systems can also be created by combining TLC systems with other systems such as mass spectrum analysis and Fourier transform infrared.1.2 Ink AnalysisInk analysis is a very important forensic procedure. It can reveal useful cultivation some questioned document. Modern inks contain many substances which are aimed at improving the ink. The most important component of the ink is the colouring material. It comes in the form of a tarnish, pigment or a combining of both. Dyes are oi l-soluble in the swimming body of the ink, also known as the vehicle. Pigments are delicately ground multi-molecular granules that are insoluble in the vehicle. The vehicles composition affects the flowing and drying qualitys of the ink and can consist of oils, solvents and resins.1.3 Chromatography StudiesDjozan et al developed a new and firm method for the polariation of inks on a questioned document. They designed specific word picture analysis software for evaluating thin layer chromatograms. They sampled forty-one gloomy ballpen pen pen pen pens which were purchased from their local markets in Iran ( circuit card 1).They origin wrote a circumference of diameter 5 mm uniformly by pen on a paper. single fourth of this was then punched out for rootage. They carried out pedigree in 1 ml glass tubes and added 0.1 ml of methanol. This was then vigorously shaken for 1 min. the ink component was then fully dissolved in methanol. The supernatant methanoic solutions were t hen used to spot the TLC plates. A pinhead sample of paper with equal dimensions was also treated in the same way.Table 1. itemization of blue ballpoint pens studiedList of blue ballpoint pens studied1 Cello pyramid 0.7 mm fine TC ball2 OBA3 AIHAO4 Bic 015 Cenator6 PARKER7 A.T.CROSS FINE8 Pelikan STICK 9189 Marvy SB-10 1.0 mm10 Bic 0211 PIANO crystal12 My pen 2001 PENS High Quality Bluce CE13 AIBA14 STAEDTLER commove 430M A IRAN15 Reynolds Medium 048 France16 EIFEL Elegance17 CASPIAN STICK 2001 M18 STABILO liner 30819 FABER-CASTELL 1.0 mm Medium (transparent)20 BIC 0821 Bocheng A-10022 SCHNEIDER TOPS 505 M Germany23 FIBER-CASTELL 1.0 mm Medium24 MILAN PI 1 mm25 Reform26 PAPER = MATE FLEXGRIP ultra MED27 PARKER UK28 CANDID-DINI 285329 STABILO-galaxy 818 M30 No name31 No name32 Zebra Rubber 10133 SANFORD SAGA34 Bensia35 Girls36 EUROPEN37 PARS swiss Refill 60638 STAEDTLER overreach 430 M TBRITAIN39 Lus HF 50040 No name41 STABILO bill 508TLC analysis was carried out on Merck (Darmst adt, Germany) 20 cm x 20 cm silica gel 60 TLC plates without fluorescent indicator. The plates were activated at 60 C for 20 min and immediately spotted after cooling in a desiccator. The plates were developed in a developing chamber. The mobile phase used was ethyl ethanoate/ absolute ethanol/ distilled water (703530, v/v/v). Chromatographic development of the plates was carried out at room temperature for 40 min. All mobile phases were prepared daily with analytical grade chemicals. bountiful was prepared to supply the tank for each run. The plates were air-dried after development. The separated compounds were visible on the plate by their vivid colour and the plates were scanned into a seer using an office electronic scanner.An IBM compatible PC (penitentiarytium IV) with a 2.6 gigacycle per second microprocessor, 256 MB random access memory (RAM) and a hard record book with 40 GB capacity for external storage was used for treat the colour reachs. The computer was equipped with an on-board graphic card (NviDiA Geforce 7300LE) and a scanner (CanoScan 4200F) was connected to the computer for scanning (300 dpi) TLC plates as digital images. The images were deliver as bmp files. Matlab (Version 6.5, The Math Works, Inc.) was used to write a new syllabus to process the previously saved images.Previous studies indicated that Pyridine is the solvent used with ballpoint pen inks. Djozan et al preformed extraction with different solvents using various extraction modes. These modes were preoccupation of paper into solvent and simple agitation for 1 min, ultra-sound help extraction and micro-wave assistance extraction. The results showed that the immersion of paper into methanol or pyridine and simple agitation resulted in complete extraction of the inks from paper (Table 2).Table 2. List of solvents used for extraction of ink components from paperSolventSolubility of ink colours ethyl group ethanoateEthanolAcetic acid propanonebutanol1,2-DichloroethaneButy l acetate rayonTetrachloroethaneAcetyl acetateCyclohexane wood spiritPyridinesome reasonably sparingly slightlySlightlySlightlySlightlySlightlySlightlySlightly dissolubleSolubleNo improvement was put using ultra-sound or micro-wave assisted extraction. Methanol was chosen as the extraction solvent due to the safety of the solvent. The selection of the plate was down to the fact that silica gel plates provided the scoop out resolution of dye spots. They selected five mobile phases (Table 3) and found that ethyl acetate/ absolute ethanol/ distilled water (703530, v/v/v) was effective in separating nearly all the dye mixtures. The spot capacity obtained was more than 15.Table 3. Different solvent systems used to develop plateSolvent SystemRatioSpot capacityButanolethanolH2OEthyl acetatecyclohexanemethanolNH3Ethyl acetateButanolNH3Ethyl acetateethanolH2OToluene propanoneethanolNH35015107015105603557035303060729510155Fig. 1. Typical TLC results of 10 different ink samples (Djozan et a l, 2008)Fig. 1. shows a typical chromatogram that they achieved in their experiment. To confirm complete separation of all components in the studied sample, two-dimensional (2D) TLC was carried out using various solvent systems. The results proved that the one-dimensional (1D) TLC is able to provide sufficient separation.The first stage carried out was colour image normalization. A habit of the input images was computed that is invariant to confounding scene properties but was discriminative with respect to desired scene information. The calculation is as followsStage 2 is to compute a colour image profile. The intensity profile of an image is the train intensity values taken from regularly spaced points along a line segment in an image the intensity values are interpolated for points that dont fall on the centre pixel they computed an intensity profile for r, g and b images along the line passing through the centre of the image on the chromatographic development straight of each ink spot.Fig. 2. RGB characteristic of an ink after TLC (Djozan et al, 2008)In stage 3 the colour image profiles were correlated. The intensity profiles were considered as sequences and the normalized cross-correlation of sequences were computed. Cross-correlation is a measure of similarity of two signals. It is used to find features in an unknown signal and compared to a known signal. It is reckon as follows for discrete functionsEq. (1)For image-processing applications in which the brightness of the images can be due to lighting and exposure conditions, the images can be first normalized. It is calculated as followsEq. (2)Stage 4 involved computing image similarity. The heavy mean of and were computed as followsEq. (3)The ability of the method to differentiate between various blue ballpoint pens was evaluated by comparing the similarity of different inks according to Eq. (3).Fig. 3. Screen shot of Matlab software running (Djozan et al, 2008)Fig. 4. All possible combination of c omparing inks with TLC-IA (Djozan et al, 2008)In 2006 Liu et al published a paper on the classification of somber gel pen inks by ion-pairing high-performance liquid chromatography. They stated that black gel inks usually contain several dye components. These components all have different colours and are mixed together equilibriumally to give the black colour.They used reverse-phase ion-pairing high performance chromatography (RP-IP-HPLC). It was make in such a manner as the dyes couldnt be change on the C18 column due to their high polarities. The maximum UV ducking draws of the black gel pen inks obtained were between 500 and 700 nm. The wavelength of the sensor was coiffe to 580 nm as most of the dyes had a maximum UV surface assimilation near 580 nm.They investigated the influence of both volatile and non-volatile ion-pairing reagents on the HPLC analysis of black gel pen ink dyes. All the reagents had different alkyl chain, ammonium ion acetate, triethylamine (TEA), tributylamine (TBA), dihexylamine (DHA) and tetrabutylammonium bromide (TBABr). The results revealed that the dyes were nearly not retained using ammonium acetate or TEA as the ion-pairing reagent. Using TBABr, TBA and DHA as the ion-pairing reagent, one after another, the dyes were separated. TBABr was selected as the ion-pairing reagent as the retention times were shorter than the others and sharper peaks were obtained.They also investigated the damp solution engrossments and the effect of pH on the separation. The optimum result was 40 mmol/L TBABr fan solution (pH 7) with acetonitrile as the organic modifier for IP-HPLC analysis and an identical proportion of the buffer and acetonitrile (v/v = 4060) at a flow rate of 1.0 mL/min. these optimum conditions were used to separate 50 dye-based black gel pen inks by IP-HPLC.Liu et al carried out another study on ion-pairing HPLC in 2006. This time, however, they studied the degradation of blue gel pen dyes and also used electrospra y tandem mass spectrometry.They used ion-pairing reversed phase liquid chromatography as the inorganic compounds they were analysing have weak retention on the unexceptional reversed stationary phases when separating on HPLC. This is due to their high polarities. The UV detector was set at 580 nm for the analysis as most dyes have a normal maximum absorption near 580 nm. The UV absorptions of the fluorescence lightening reagents in paper are usually below 500 nm and they had no interference for the detection of the gel pen dyes at 580 nm.Fig. 5. Chromatograms of blue gel pen inks using different ion pairing reagents (Liu et al, 2006)The tested various mobile phases eluent A eluent B (acetonitrile) = 5050 (v/v) eluent A was the buffer of ion pairing reagent with concentration of 40 mmol L1 (pH 7.0), and the ion pairing reagent was (a) ammonium acetate, (b) TEA acetate, (d)TBA acetate, (e) DHA acetate and (f) TBABr, respectively. (c) Ammonium carbonate as eluent A (40 mmol L1, pH 9.5 ) and eluent Aeluent B (acetonitrile) = 5050(v/v). they found that 10 mmol-1 TBA acetate (pH 7.0) was suitable ion-pairing agent for the purpose and ink samples stored in different conditions were analyse by IP-HPLC. Significant changes of ink composition were observed. The noticed that the natural senior inks had the similar but weaker degradation trend than the light aged inks. They used HPLC-MS/MS with ammonium carbonate as ion-pairing reagent to obtain the information of the light aged inks and their photodegradation mechanism.In 1994, Varshney et al analysed ink from typed script of electronic typewriters by HPTLC. They used script from seven electronic typewriters. They used the incidental Rf values and in-situ visible spectra of each resolved band of all the chromatograms indicated that the same chemical composition is being used in six typewriter ribbon inks. However, the seventh one is completely different.Fig. 6. Wavelength maxima values of in-situ visible spectrum ban ds of electronic typewriter scripts (Varshney et al, 1994)Fig. 6. shows the densitograms obtained after scanning and integration of the chromatograms of tracks of individual typewriters and blank paper. The seven electronic typewriter inks could be categorised into two groups after analysis. The first group resolved the sample to four bands including the base. The second group did not resolve the samples at all with the solvent systems used.Several varieties of blue ballpoint pen inks were analysed by HPLC and IR spectrometry by Kher et al in 2006. The chromatographic data extracted at four wavelengths (254, 279, 370 and 400 nm) was analyzed individually and at a combination of these wavelengths by the soft independent exemplar of class analogies (SIMCA) technique. They used principal components analysis (PCA) to estimate the separation between the pen samples. Linear discriminant analysis (LDA) measured the probability with which an observation could be assigned to a pen class. T he best resolution was obtained by HPLC using data from all four wavelengths together, differentiating 96.4% pen pairs successfully using PCA and 97.9% pen samples by LDA. PCA separated 60.7% of the pen pairs and LDA provided a correct classification of 62.5% of the pens analyzed by IR. They stated that HPLC coupled with chemometrics provided a better discrimination of ballpoint pen inks compared to IR.Kher et al effectively combined LDA and PCA to classify the HPLC and IR data. PCA gives a general idea of how different a given pair of pens is, whereas LDA can quantify the predictive ability of a generated classification model. The two techniques of PCA and LDA were shown to be complimentary to each other. The PCA and LDA results indicated that although IR cannot differentiate between all classes of pen inks, it can still provide a reasonable discrimination, which can be enhanced further by improving the quality of the spectra. The analysis of such an enhanced IR data with chemometr ic analyses would provide a valuable non-destructive wight for forensic analyses.Raman Spectroscopy StudiesMazzella and Buzini used Raman spectroscopy to analyse blue gel pen inks in 2004. They sampled 55 blue gel pens. They first separated them into two groups using a preliminary solubility test in methanol. They discovered that 36 were pigmented inks, which arent soluble in methanol, and 19 were dye-based inks, which are soluble in methanol.They applied Raman spectroscopy to the 36 pigmented blue gel inks. Raman spectroscopy is a non-destructive technique. Spectra were first obtained using the 514.5 nm argon ion laser which proved the observation of 4 different groups. They then used the 830 nm NIR semiconductor diode laser and divided the inks into three groups. They then combined the two lasers and a separation into 5 groups was obtained.They then attempted to identify the pigments contained in the gel by comparison to standard pigments. Two main pigments were detected in the analysed samples PB15 and PV23. PB 15 is pigment blue 15 and belongs to the class of phthalocyanines. PV23 is the pigment violet 23 and belongs to the class oxazines. The argon laser allowed the detection of a mixture of PB 15 and PV 23. This was a better result than using the NIR diode laser.The results showed that the same gel pen ink (same model and brand) from different geographical locations showed the same Raman spectra. However, it was stated that the Raman technique obtained low discriminating values.2. Materials and method2.1 MaterialsBlue ballpoint pensMerck silica gel 60 TLC plates (20 cm x 20 cm)MethanolEthyl acetateEthanol (absolute) opusDessicatorDeveloping chamberPuncherGlass tubes (0.1 ml)Capillary tubes2.2 Experimental13 blue ball-point pens (Table 1) were bought from a number of different shops in the town. A circle with a diameter of 5mm was written by the pen on paper. superstar fourth of it was punched out for extraction. The samples are placed in 1 ml glass t ubes. 0.1ml of methanol was added and vigorously shaken for 1 min. The ink component was fully dissolved in methanol. The supernatant methanoic solutions were used for spot application on TLC plate. A blank of paper only is also treated as was a control which was a permanent marker. TLC analyses were preformed using Alugram 20 cm x 10 cm silica gel/UV plates (Macherey-Nagel). The plates were activated at 60C for 20 min and immediately after, cooled in a desiccator, and spotted. The plates were developed in a horizontal developing chamber. The solvent system included ethyl acetate/absolute ethanol/ distilled water (703530, v/v/v). schooling was preformed at room temperature for 40 min. All mobile phases were prepared daily. later development the plates were air-dried. All 13 different pens were tested in triplicate. memory board factors were calculated using the results from the plates and photographs taken using a digital photographic camera were loaded onto the computer and ana lysed using image analysis software.Table 1List of pens analysed flakeDescription1No Brand (blue)2Pilot G-2073BIC ReAction4BIC Medium (Bought in Tesco)5BIC Medium (Bought in Dunnes)6No Brand (Purple)7Staedtler Stick 430M8Roller Pen9Papermate 1.2M10Scripto Stick Pen11Papermate Write Bros.12Comfort Touch13No Brand (Tesco Click Pen)3. Results and DiscussionBefore carrying out the experiment it needed to be researched. This research pointed out the importance of the correct solvent to retreat the ink from the document. Djozan et al used methanol as their choice of solvent after considering other solvents (Table 2). They stated that Pyridine was the reported solvent used with ball-point pen inks. However, they carried out extractions with different solvents using various extraction modes. They realised that immersion of the paper into methanol with agitation resulted in complete extraction of the inks from the paper. Methanol was also chosen because of its safety.Table 2List of solvents used for the extraction of ink components from paperSolventSolubility of ink coloursEthyl acetateSlightlyEthanolSlightlyAcetic AcidSlightlyAcetoneSlightlyButanolSlightly1,2-DichloroethaneSlightlyButyl acetateSlightlyTetrachloroethaneSlightlyAcethyl acetateSlightlyCyclohexanSlightlyMethanolSolubleOyridineSolubleDifferent concentrations of the solvent system (Table 3) were analysed to see which gave the greater separation. It was found that the concentration given by Djozan et al, (ethyl acetate, ethanol, and water (703530, v/v/v)) gave the best results. The Alugram silica Gell/UV plates were also found to work better than the suggested, Merck silica gel 60, plates without fluorescent indicator.Table 3Concentrations of solvent system investigatedNumberSolvent system1ethyl acetate, ethanol, water (703530, v/v/v)2ethyl acetate, ethanol, water (703035, v/v/v)3ethyl acetate, ethanol, water (702540, v/v/v)4ethyl acetate, ethanol, water (704025, v/v/v)Table 4Retention factors for all separ ated componentspenspot 1spot 2spot 3spot 4spot 5SolventRF1RF2RF3RF4RF51.170730.9589041.270730.9589041.270730.9589042.16269730.84931581.241942.26269730.84931581.241942.36269730.84931581.241943.1576062700.814286