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How Temperature Affects Viscosity

  How Temperature Affects Viscosity: Viscosity can be defined as the internal friction that occurs as a material flow, relative to itself....

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2017年6月27日星期二

Determination of viscosity of polymer by using Ubbelohde viscometer

Abstract: viscosity experiment notes: 1) the temperature of constant temperature water bath has a great influence on viscosity measurement. The temperature fluctuation of water bath should be within the range of + 0.05 DEG C, and the temperature of the water in the constant temperature water bath should be uniform. 2) capillary Ubbelohde viscometer must use clean liquid soaked and washed with water, can be used for drying the rear 105. 3) must be fixed on the vertical viscometer in constant temperature water bath. Otherwise, it will affect the velocity of flow and cause the error of measurement result. 4) after each dilution, the liquid in the viscometer must be mixed evenly. The method is to clamp the hose of the C tube, receive the gas from the B tube, mix the liquid in the D ball of the viscometer evenly, and then rinse the liquid in the D ball.

1. Basic principles
1.1, the viscosity of polymer solutions has the following definitions:

(1): relative viscosity ηr representation as . Among them, η0, it’s the pure solvent viscosity. η is the viscosity of solutions at the same temperature. ηr is a dimensionless quantity.
For low shear rate polymer solutions, the values are generally greater than 1. Obviously, with the increase of the concentration of ηr solution will increase.
(2): specific viscosity: indicated by ηsp, is compared with the solvent viscosity increase the fraction.
(3): Specific viscosity
Ratio of solution to specific viscosity to solution concentration

                          











The viscosity of the solution when the solution is infinitely diluted is independent of the concentration, and its dimension is the reciprocal of the concentration cm3/g

1.2 One point method
2. Device diagram



















As a common three branch glass viscometer.It has a capillary with a diameter of R and a length of L. At the top of the capillary there is a small ball with a size of V. There are lines a and B on the top and bottom of the ball. In the experiment, the C pipe is closed when the liquid is pumped from the A tube to the B tube, and then the C tube is passed through the atmosphere so that the liquid level at the lower end of the capillary drops. The liquid in the capillary forms a gas suspension column and flows down the pipe wall at the lower end of the capillary. This can avoid the exit turbulence as possible, and the equivalent average (which is the liquid column to suspension column height) with A tube liquid level.
Following the principle of determination of the viscosity of the liquid to be tested: adding self A tube, B tube by liquid suction to the a line above the B pipe through the atmosphere, let it flow down, record level through a and B line t.

3, Operation procedures and matters attention
Take the measured liquid along the inner wall of the tube into the A viscometer ball D. The viscometer is vertically fixed in a constant temperature water bath. Water temperature should be 25 - 0.05 DEG C, the water level higher than the buffer (upper B tube ball ball), placed 15 minutes, B tube and C tube are respectively connected with a latex tube, C tube hose clamp, B pipe mouth pumping; the test solution level increased to buffer the ball slowly part of the first open B nozzle, and then release the C nozzle, the test solution in the tube falls naturally, with a stopwatch accurate record level self-testing a down to fixed line by line B at the outflow time, were determined for two times, two times the difference should not exceed 0.1 seconds, averaged two times for the test solution the outflow time (T).
Matters needing attention
1) the temperature of the constant temperature water bath has a great influence on the viscosity measurement. The temperature fluctuation of the water bath should be within the range of + 0.05, and the temperature of the water in the constant temperature water bath should be uniform.
2) capillary Ubbelohde viscometer must use clean liquid soaked and washed with water, can be used for drying the rear 105.
3) must be fixed on the vertical viscometer in constant temperature water bath. Otherwise, it will affect the velocity of flow and cause the error of measurement result.
4) after each dilution, the liquid in the viscometer must be mixed evenly. The method is clamped C pipe hose, B tube gas, the mixed liquid D in uniform ball viscometer, ball, and then pumped D buffer liquid in the washing ball viscometer determination of ball (A and B line between the ball on the B tube), capillary 2-3 times.


Kent Yuan (Mr.)
Hangzhou Zhongwang Technology Co., LTD.
 /Wahtsapp: +86 15068109723  lei@zonwon.com 
 

    
Coyp right by @Hangzhou Zhongwang Technology CO.,LTD

2017年6月5日星期一

Using method and application of Ubbelohde viscometer

Using method and application of Ubbelohde viscometer

Abstract: the viscosity coefficient of liquids, referred to as viscosity, reflects the size of the frictional force in the fluid, i.e., the magnitude viscosity of the fluid. This article describes the research method of using Ubbelohde viscometer fluid viscosity measurement size and application.


The molar mass of polymers not only reflects the size of polymer molecules, but also directly relates to their physical properties. It is an important but basic parameter. Unlike common inorganic or low molecular organic compounds, polymers are mostly mixtures of macromolecules of different molar masses, so the molar mass of a polymer is usually a statistical average.

There are many methods to determination of high molar mass, while the average molar mass obtained by different methods are also different. By comparison, the viscosity method is simple, easy to operate and has very good experimental accuracy. It is one of the most common methods. With the method of molar mass is called viscosity average molar mass.

Using method of Ubbelohde viscometer
1.     Take out the Ubbelohde viscometer, with a solution made of certain concentration in accordance with the provisions of the rules, and go through with a 3 sintered glass funnel filtration, discarding the initial filtrate (about 1ml);
2.     The successive filtrate (not less than 7ml) along the dry and clean Ubbelohde viscometer  2 wall into B tube, the viscometer is vertically fixed on the constant temperature water bath (bath temperature should be 25 - 0.05 DEG C unless otherwise specified), and make the water level higher than the ball C, placed in 15 minutes;
3.     The nozzle 1 and 3 are respectively connected with a latex tube, pipe clamp 1 hose, since the nozzle 3 pumping, the tested liquid solution slowly increased to the ball the central C, first open the orifice 3, then open mouth 1, the testsolution in tube falling, with a stopwatch accurate record the level of m<[1]> decreased to self testing fixed line by line m<[2]> at the outflow time;
4.     Repeated determination of two times, two times the difference between the value of determination shall not exceed 0.1 seconds, averaged two times for the test solution outflow time (T).
5.     learn from the No. 3 vertical molten glass funnel filtration solvent, the same operation, repeated determination two times, two times the measured value should be the same, for the solvent outflow time (T<[0]>), according to formula to calculate the intrinsic viscosity.

Study on Application of Ubbelohde viscometer

1. Molecular weight determination:
Because the specific viscosity is closely related to the viscosity average molecular weight of polymers, the intrinsic viscosity is a very important molecular weight parameter
Analysis of the morphology

2. Polymers in solution:
Polymer in different solvents, due to different degrees of expansion, so that the value of its intrinsic viscosity is different, batch difference can reach as much as 5 times. According to the characteristics of viscosity in different solvents, we can determine the initial conformation of the polymer in a solvent, especially some biopolymer, this phenomenon is very obvious

3. Criteria for the degree of polymer synthesis
When the polymer is polymerized by solution polymerization, the concentration of the solution increases as the degree of polymerization of the polymer increases. Therefore, in the experimental process of the synthesis of the polymer solution, can be in different stages of sampling, determination of kinematic viscosity solution by Ubbelohde viscometer, used as a criterion of polymerization degree.


4. Kinetic study of polymerization


Kent Yuan (Mr.)
Hangzhou Zhongwang Technology Co., LTD.
 /Wahtsapp: +86 15068109723  lei@zonwon.com 
 

    
Coyp right by @Hangzhou Zhongwang Technology CO.,LTD

2017年5月15日星期一

What instrument can be used to measure kinematic viscosity?


The kinematic viscosity is the viscosity of the fluid and the same temperature of the fluid density ratio. The unit is (m^2) /s. Use the lower case letter v.
There are three methods for determination of viscosity, kinetic viscosity, kinematic viscosity and conditional viscosity.

Dynamic viscosity: ETA t two liquid layer is 1 cm apart; the area was 1 (CM) relative speed of 1 cm / sec generated resistance units for g / cm / sec. 1 g / cm sec =1: general industrial dynamic viscosity unit expressed by poise.

Kinematic viscosity: when the temperature is t degrees centigrade, the kinematic viscosity is indicated by the sign gamma. Kinematic viscosity is widely used in the determination of jet fuel oil, diesel oil, lubricating oil and other liquid petroleum products, petroleum products after use of lubricating oil, crude oil viscosity, viscosity was determined by capillary viscometer method.


IVS300 Viscometer
 Hangzhou Zhongwang Technology Co.,LTD designed the automatic test instrument IVS300 based on ISO1628/ ASTM D 2857. This machine was widely used in polyester (PET), quality control and testing of raw materials, nylon, silicone polymers such as polyacrylamide industry, containing all the viscosity of the formula can be obtained directly by viscosity, viscosity, relative viscosity, characteristic viscosity and viscosity average molecular weight of the.


In the kinematic viscosity automatic tester IVS300 system uses the modular design, mainly by the viscosity measurement unit, precision constant temperature bath, through the cooler and the main controller and the viscosity of special software modules;



Automatic Viscometer Measuring Unit
Each measuring unit is an independent system, and all test procedures are completed by each test head. The test unit and the main controller are connected only through one data line;
The pressure method is adopted to lift the sample; the loading and unloading of the viscosity tube adopts a unique pressing block mode;
The pump pressure can be automatically adjusted by software according to the viscosity of the sample;
The measuring fiber is made of stainless steel smart fiber, which can automatically change the intensity of the fiber because of the different colors of the sample; 
The viscosity thermostat is designed and the measuring zone isolation constant temperature zone, will affect the temperature of the bath temperature in the process of fluctuation on the measurement is reduced to the minimum, to ensure a constant level measurement of temperature field and temperature region;

Constant Water Bath




Viscosity constant temperature tank has high and low water alarm function. The inner tank is made of mirror stainless steel, large double toughened hollow glass observation window and LED lighting;
Cooler adopts the most advanced PTL refrigeration technology, continuous operation life of more than 50 thousand hours.







IVS300 Software 
Hangzhou Zhongwang Technology Co.,ltd Software is very powerful, with all sectors of the different viscosity formula, including the Bill Meyer formula / Hagen Poiseuille formula / formula / Hagens Mark Houwink formula / Martin / Solomon - Xiuta formula formula. Customers can be automatically calculated according to needs; Chinese menu; unattended after starting, automatic continuous testing, until the finish of the test data; intelligent identification, such as measurement data does not match the user requirements with buce function; software with rights management, protection of important data will not be free to modify the instrument;

Technical parameter

1. Bath temperature fluctuation uniformity: + 0.01
2. Bath control temperature range: 5-55 DEG C
3. Ting accuracy: 0.01S
4. Measuring viscosity range: 0.35-5000 mm2/s (specific range of use and supporting viscosity tube related)

5. Time measurement range: 0... 9999.99S



Kent Yuan (Mr.)
Hangzhou Zhongwang Technology Co., LTD.
 /Wahtsapp: +86 15068109723  lei@zonwon.com 
 

    

Coyp right by @Hangzhou Zhongwang Technology CO.,LTD

2017年5月8日星期一

Determination of relative molecular mass of water soluble polymer by viscosity method

Determination of relative molecular mass of water soluble polymer by viscosity method

Abstract: in the study of polymers, the relative molecular mass is an indispensable important data Because it not only reflects the size of polymer molecules, but also directly related to the physical properties of polymers.

In the study of polymers, the relative molecular mass is an important data. Because it not only reflects the size of polymer molecules, but also directly related to the physical properties of polymers. However, unlike ordinary inorganic or low molecular organic matter, the polymer is a mixture of different molecular weight, so the relative molecular mass is usually an average value. There are many methods to determine the relative molecular weight of polymer. Compared with other methods, the viscosity method is simple and convenient to operate.

The viscosity of polymer solution is particularly large, because its molecular chain length is much larger than that of the solvent molecule, and the solvent is added to make it more resistant to friction.

In the flow of viscous liquid, it is necessary to overcome the internal friction resistance and work. The size of the coefficient of resistance available viscosity of viscous liquid in the flow process (the viscosity) to express (kg M-1 S-1).

The viscosity of dilute polymer solution is a reflection of the size of the internal friction force. The pure solvent viscosity reflects the internal friction between the solvent molecules, denoted ETA 0, polymer solution viscosity is high internal friction between the molecules, polymer molecules and solvent molecules and internal friction between three and 0. At the same temperature, usually ETA > ETA 0, relative to the solvent, the viscosity of the solution increases the fraction called viscosity, denoted as SP, i.e.

1The ratio of the viscosity of the solution and the pure solvent viscosity called relative viscosity, denoted R, i.e.

2The viscosity behavior of ETA R is also reflected in the solution, and SP means has been deducted from the solvent internal friction between the molecules effect only reflects the polymer molecules and solvent molecules and polymer molecules between the internal friction effect.
The polymer solution viscosity eta SP tended to increase with increasing concentration of C. For comparison, the unit concentration shows the specific viscosity of SP / C is called viscosity, R / C and LN ETA is known as logarithmic viscosity. When the solution is diluted, the polymer molecules are far apart from each other, and their interaction can be ignored



3[η] called intrinsic viscosity, it reflects the polymer molecules and solvent molecules in dilute solution of infinite internal friction between the size and shape, its value depends on the properties and polymer molecules of solvent. Because R and SP are both ETA ETA dimensionless quantity, so their unit is the reciprocal of concentration of C units.
In the dilute polymer solution is sufficient, SP / C and C / C and LN R and C respectively conform to the following formula:
4

5The two and the Huggins and Kramer are the constants in the. This is the two linear equations, the SP / C ETA on C or ln / C ETA r in C mapping, extrapolated to C=0 is the intercept []. Obviously, for the same polymer, the two linear equations are extrapolated to the same point, as shown in figure 1.


Figure 1: extrapolation method [η]        Figure 2: viscometer

The relationship between intrinsic viscosity and polymer molar mass of polymer solution, usually expressed with two parameters of Mark - Houwink equation:



6) In the formula  means the average molecular weight of viscosity, K is the proportionality constant, and alpha is an empirical parameter related to the molecular shape. The value of K and alpha is related to the temperature, the properties of the polymer and the solvent. The value of K is affected by temperature obviously, alpha value mainly depends on the polymer coils in a certain temperature, the degree of a stretch of solvent. K and alpha can be determined by some absolute experimental methods (such as membrane osmotic pressure, light scattering, etc.).

The capillary tube method was used to determine the viscosity, and it was obtained by measuring the time required for a certain volume of liquid to flow through a capillary with a certain length and radius. Ubbelohde viscometer used in the experiment as shown in figure 2. When the liquid passes through the capillary under gravity, it follows Poiseuille's law:


7) Type of eta (kg M-1 s-1) is the viscosity of the liquid; liquid density; capillary length; capillary radius; outflow time; the average height of liquid column of liquid flows through the capillary; for the acceleration of gravity; V is the volume of liquid flows through the capillary; and the geometric shape of the instrument is constant. When take m=1.

For a specified viscometer, many parameters are specified, so that
,.
So 7) can be changed as,
8) In the Formula , when
,the equation on the right side of the second can be ignored. The density of the solution
 is approximately equal to the solvent density
. In this way, the T and t0 of the solution and solvent can be calculated
:  

9) So the only solution was determined and solvent in capillary outflow time can be obtained by ηr.

Operation steps
1 cleaning equipment
The viscometer with lotion, tap water and distilled water clean, pay special attention to the capillary, rinse with ethanol, and then dried standby.
It takes longer to dry the viscometer, especially for a long period of time. After drying, the viscometer is placed in a constant temperature bath and is clamped vertically with an iron clamp.
2 polyvinyl alcohol solution
Accurate weighing about 1g solid polyvinyl alcohol, into the beaker, add 60mL distilled water to dissolve, can be properly heated to accelerate the dissolution, to be solid polyvinyl alcohol completely dissolved, the solution (solution after cooling) into 100mL volumetric flask volume.
1.0111g polyvinyl alcohol is said to be solid and dissolved in an electric furnace. After the dissolution of polyvinyl alcohol 10min. Transferred to the capacity of the bottle at 35 degrees Celsius under constant temperature and volume, the volume of the solution was found to have some foam.
3 constant temperature
Open the thermostat, set the temperature of 35 + 0.01. The viscometer (Figure 2) in the thermostat temperature 10min (note that vertically). Pure water as well as samples to be measured at 35 degrees C.
In addition, the utility model can be conveniently placed in a constant temperature water tank with a conical bottle filled with distilled water.
4 Determination of solvent outflow time t0
The water is injected into the viscometer 20mL, and the temperature is measured after 2 minutes. The method is as follows: the C tube is not ventilated. Wash the ear with a ball at the upper end of the suction pipe B, the water from the F ball by D ball, E ball, capillary pumped to G at 2/3; the clip on the release of C tube, the ventilation, the D solution in the ball back into the F ball, the capillary suspended above the liquid; the liquid falls above the capillary. When the concave surface the lowest scale a flows through the line, immediately press the stopwatch start time, stop time to B. Note the time required for the liquid to flow through a, B. Repeated measurement three times, the deviation is less than 0.3s, the average value is t0.
Distilled water is taken from the 3 in the conical flask, to ensure that the liquid drops when the liquid level does not bubble, the data recorded in 5.
5 Determination of time of solution outflow
Drying viscometer, with the pipette has been a good solution in advance of 10mL, the A tube into the viscometer, in 25 degrees of water temperature for about 2 minutes, the determination of the outflow time of three times, the average.
Pure solution viscosity is very large, with the ear when the ball to slowly inhale to rise to the surface of the G ball, otherwise the bubble will be a lot of.
6 Determination of the outflow time of different concentration solution
2, 3, 10 mL distilled water was added to the viscometer, and the T values of different concentrations were measured by the above methods, respectively. After each dilution, the liquid is mixed (2min) with an ear washing ball, and the E ball, G ball and capillary part of the viscosity are repeatedly washed.
In accordance with the steps in the operation 3-4 times after the solution is roughly mixed. Data records see 5.
7 cleaning equipment
Turn off the power supply, clean the viscometer 3 times, fill it with water. To ensure that the viscometer is not used when it is clean, otherwise there is a foreign body for a long time to clean up the impact of experimental results.
Matters needing attention
1 the use of black viscosity timing, in the same viscometer to determine a series of concentrations into a simple proportional relationship between the outflow time of the solution. In order to avoid the volume change caused by the temperature change, the solution and the solvent should be removed at the same temperature.
2 every time when adding solvent dilution solution, the viscometer must be mixed in the liquid, but also to the solution to the E line above the ball two times, wash capillary, otherwise the time of the solution is poor repeatability.
3 in the use of organic matter as a solvent for the polymer, the polymer solution contained a glass instrument, should be the first to use this solvent soaking and washing to be washed and moist, dry polymer organic material such as solvent, can be used to soak chromic acid, or organic materials are made of chromium in pickling solution of potassium dichromate reduction, lotion will fail.
4 viscometer must be clean, such as hanging on the capillary wall with water, blowing dryer.
5 Determination of the viscometer to be placed vertically, otherwise affect the accuracy of the results.
6 in this experiment, the dilution of the solution is carried out directly in the viscometer, so the solvent must be in constant temperature with the solution in the same temperature tank, and then accurately measured with the pipette and fully mixed can be measured.


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2017年5月2日星期二

Determination of polymer solution properties - Determination of density gradient crystallinity of the polymer


Determination of polymer crystallinity by density gradient method

Polymers due to its long chain structure and molecular weight dispersion and other reasons, to form a complete crystal is very difficult, so for crystalline polymers generally can only form part of the crystal, often using crystallinity to describe the degree of crystallization , It is an important parameter of crystalline polymer. Crystallinity has an important effect on the physical and mechanical properties of the material such as strength, hardness, transparency, heat resistance, air permeability, solubility and so on. The crystallinity of the material is not only related to its chemical structure, such as the regularity of the chain, but also has a great relationship with the process conditions of the forming process, including the cooling rate, tensile orientation, nucleating agent and so on. Therefore, in order to study the crystallization of the polymer processing technology on the performance of the crystallization of the measurement is an indispensable link. Crystallinity in the industry is also often used as an intermediate indicator of polymer products.
The method of measuring the crystallinity is X-ray diffraction, calorimetry, infrared spectroscopy and density method. Among them, the density method is one of the most commonly used methods because of its simple equipment, convenient operation and data processing and high The accuracy and has been widely used. In the density measurement using density gradient method with high precision measurement, you can simultaneously compare the measurement of multiple samples, with a good density tube can be used repeatedly, etc., especially for industrial analysis.

First, the purpose of the experiment
1, master the density gradient method for the determination of polymer density and calculate the principle of crystallinity and methods;
2, master the correct use of the proportion of bottles.

Second, the experimental principle
Crystallinity refers to the weight or volume percent of the crystalline fraction in the crystalline polymer. Since the boundary between the crystalline phase of the polymer and the amorphous phase is not clear, the physical meaning of the crystallinity is also unclear. Different measurement methods have different scales for the discrimination of the crystal phase and the amorphous phase, and the crystallinity is different The The density method assumes that the crystalline polymer consists of a crystalline region and an amorphous region, with a specific capacity (or density) additive between them. The ratio of the crystalline fraction and the amorphous part is VC and Va, respectively. Capacity V is
V = XcwVa + (1 - Xc w) Va (1)
Where X c represents the weight crystallinity (the fractional fraction of the crystalline fraction), and the above equation can be written as
            Xcw = (2)
The density of the crystal and amorphous regions is ρc and ρa, and the density of the sample is ρ, then the above equation can be written as
XCw = (3)
Similarly, the volume crystallinity Xcv is obtained
          XcV = (4)
From the formulas (3) and (4), it is known that if the density ρc of the completely crystalline polymer sample and the density ρa of the completely non-crystalline polymer sample are known, it is only necessary to determine the density ρ of the polymer sample Its crystallinity.
In this experiment, the density of the polymer sample was measured by the suspension method, that is, under the constant temperature condition, the proportion of the two liquids which could be completely miscible was adjusted in the test tube with the polymer sample. Floating, but suspended in the middle of the liquid, according to Archimedes law we know that the density of the mixed liquid at this time and the polymer sample conspiracy equal to the use of pycnometer to determine the density of the mixed solution, you can get the polymer sample density.

Third, instruments and reagents
instrument:
1 set of constant temperature sink
        25ml of the weight of the bottle
        Dropper 2 root
        Tube 50ml 1 root
        One glass stir bar
drug:
Polyethylene (PE) industrial products
Ethanol Chemistry Pure 30 ml

Fourth, the experimental steps
1, the thermostat sink to (25 ± 0.1) ℃.
2, the test tube, dropper and glass stir bar according to Figure 3.3 device.
Add about 25ml of ethanol in the tube, and then add a polymer test
Like, with dropper to add distilled water, while moving up and down stirring bar,
So that the liquid mixture evenly, the first water speed can be faster, when being
When the sample was slowed down, the sample was slowly dripping
Water. (If the drop in excess, you can use another dropper back to the drop of ethanol) Figure 3.3 Schematic diagram of the experimental device
Until the sample does not sink nor float, suspended in the middle of the mixed liquid, for several minutes, then the density of the mixed liquid is the density of the polymer sample. The density of the liquid was measured with a pycnometer. Repeat the above procedure to determine the density of the other sample.

3, the determination of mixed liquid density. First use the analytical balance called the weight of the weight of the weight of the wafer W0, and then remove the stopper, filled with the measured mixed liquid, cap stopper, into the thermostat tank, the excess liquid from the capillary overflow. With the filter paper to wipe the liquid outside the capillary, when the temperature reaches equilibrium, from the thermostat out of the pycnometer and wipe the liquid outside the bottle, when the temperature
  
 Figure 3.4 Schematic diagram of the pycnometer
1. Cork Capillary; Bottle body

After the balance, from the thermostat out of the pycnometer, and wipe the liquid outside the bottle, said the liquid after the weight of the weight of the bottle after the W1. Pour the liquid in the bottle, washed with distilled water several times and then filled with distilled water, constant temperature, dry the bottle, said the weight of the weight of the bottle after the water W water, the liquid density ρ according to the following formula:
 Ρ = (W1 - W0) ρ water / (W water - W0) (5)

Fifth, data processing
1, according to formula (5) to calculate the PE sample of the plot for capacity.
2. Calculate the crystallinity of PE according to formula (3) and (4).
    Known: PE 20 ℃ when
               VC = 1.009 cm3 / g Va = 1.233 cm3 / g
               25 ℃

               VC = 1.013 cm3 / g Va = 1.161 cm3 / g

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