CHINAPLAS, recognized as Asia's No. 1 & world's No.2 plastics and rubber trade fair by the industry, will hold its 30th edition in 2016. To celebrate the reach of the milestone, there will be more attractions and celebration activities at the show for all to join!
Looking back, when CHINAPLAS was held for the first time in Beijing in 1983, the exhibition area was only 2,000sqm, and 90% of the exhibitors were from overseas. At that time, the production technology in China was still at a very low level, CHINAPLAS visitors mainly came to learn the advanced technologies from overseas countries. Today, China has become a big manufacturing country with strong production ability, and is exporting the most plastics and rubber machineries in recent years. In the past three decades, CHINAPLAS has been moving forward together with the China market, and has developed into a platform for the showcase of both overseas technologies and Chinese machineries for export. Its international nature attracts overseas visitors from more than 150 countries and regions, which accounts for nearly 30% of the show's visitors. CHINAPLAS will continue to keep abreast of the trends in the dynamic environment, and lead the industry to cope with the changing world.
Greenovation for a Smart Future
Like other manufacturing industries in China, plastics and rubber industries are facing transformation to meet the new era of intelligent production. The world's leading manufacturing countries have launched national strategic plans to meet the challenges in the new era and to strengthen their industrial competitiveness. Examples include "Industry 4.0" of Germany, "Advanced Manufacturing Partnership" of USA, and "New Robot Strategy" of Japan. China also launched the "Made in China 2025" strategic plan recently to boost its industrial growth, with the aim to comprehensively upgrade Chinese manufacturing industries. It is not hard to find that intelligent manufacturing plays a vital part in all of these national plans in adapting to new market environment. CHINAPLAS as a leading plastics and rubber trade fair always moves ahead together with the industry. The new show theme "Greenovation for a Smart Future" signifies that the show content next year will focus on green and innovative technologies, as well as intelligent manufacturing solutions in response to the development of the industry. With more new and high-end technology on display, the show can better support enterprises to explore business opportunities.
The biggest ever with more attractions
The 30th CHINAPLAS will be held from 25 to 28 April, 2016 at the Shanghai New International Expo Centre, PR China, with an exhibition area over 240,000sqm, and more than 3,200 exhibitors are expected. The show is supported by a number of country and region pavilions, including Austrian, German, Italian, Japanese, Korean, Swiss, Taiwanese, and USA Pavilions. With broader range of exhibits, the number of theme zones will rise to sixteen, among which the "Automation Technology Zone", "Composite & High Performance Materials Zone" and "Recycling Technology Zone" are all new to the coming show in Shanghai. Intelligent production lines and systems, industrial robots, high performance materials, composite materials, the latest and most complete recycling solutions as well as other plastics and rubber technology breakthroughs will be showcased under one roof.
Celebration Activities Rolling Out, Stay Tuned!
To celebrate the 30th edition of CHINAPLAS, apart from more show attractions at the fairground, there will also be a series of celebration activities for all to join. These activities are rolling out soon and will last until the next year. Stay tuned with us by checking out for our latest posts on CHINAPLAS official website!
Limited exhibition space left, reserve now!
Online space application is now available, as response is overwhelming, space is running out fast. Interested parties are advised to submit immediate space reservation on our official website to enjoy the quality and all-round promotion services.
For details, please visit the official show website at www.ChinaplasOnline.com
Volumetric Feeder For Extrusion Process
2016年1月10日星期日
2016年1月4日星期一
14th China International Food Processing and Packaging Exhibition
The 14th China International Food Processing
and Packaging Exhibition will be held during April 19-21th, 2016 at China
International Expo Centre. CF, cooperating with CIFE China, is the
largest event ever organized for a completed chain from equipments to products
in the field of international food and beverage market in China. In the past 14 years,CF has attracted an
increasing number of visitors in food and beverage Industry, allowing visitors
and exhibitors to communicate and cooperate successfully.
The exhibition range include:
FOOD MACHINERY
A. Food Processing
Machinery
Soft Drink Processing
Pastry
Processing
Candy
Processing
Soy-Bean Products
Processing
Fruits & Vegetables
Processing
Slaughtering Machinery
Meat
Processing
Milk Products
Processing
Brewing
Machinery
Flavoring
Processing
Fat Deep
Processing
Instant Food
Processing
Grain
Processing
Cooking Machinery
B. Processing Technology
Equipment
Selecting, Washing and Brushing
Machinery
Grinding and Separating
Machinery
Food Mixing
Machinery
Food
Homogenizer
Food Concentrating
Equipment
Food Drying and Sterilizing
Machinery
Food Frying
Machinery
Baking
Machinery
PACKAGING MACHINERY
C. Decorating Printing
Machinery
Wrapping
Machinery
Vacuum Packaging
Machinery
Forming-Filling-Sealing
Machinery
Labeling
Machinery
Strapping and Containering Machinery
Cleaning Machinery(Bottle Washing, Case washing)
Medicine Packaging
Machinery
Packaging Container Making Machinery
Packaging Materials Processing
Machinery
D. Other Relevant
Machinery
Inkjet
Printers
Testing Equipment
Transmission
Machinery
Weighing
Equipment
Equipment Components &
Expendables
Food Grade Series Compressor Oil
Date:
Apr.19-21,2016
Venue:
China International Exbition Center, Beijing, China
Tel: 86-
10-64787342 84414052 Fax: 86-010-58043750
E-mail: fengfeng99@vip.163.com
Exhibition Area: 50,000 square meters
Estimated Visitors: 70,000 persons
2014年10月7日星期二
Lubricants
In processing high melt viscosity polymers
such as polyvinyl chloride (PVC) by extrusion, milling, calendering and injection
molding, the shear forces applied cause excessive frictional heat which may
lead to serious thermal stability problems. Another problem in processing PVC
is to assure that the polymer releases from metal surfaces of the processing
equipment. To solve these problems two types of lubricants are used.Lubricants
which lower the melt viscosity and control frictional heat build-up are called
internal lubricants while substances which promote release are called external
lubricants. These materials are used in relatively small amounts since an
excess will cause processingand stability problems and structural weakness in
the ultimate product. In the processing of polymers such as PVC discrete
particles are subjected to stress and heat until there is fusion of the
discrete particles and a resulting loss of particle identity. An excess amount
of an external lubricant will tend to coat the individual particle and while
promoting a slippage between particles will delay fusion.
The role of the internal lubricant is to
reduce the internal friction within the polymeric melt, which includes reducing
heat build-up when the polymer is subjected to stress.Because of the
characteristic high melt viscosity of rigid PVC an internal lubricant is
usually viewed as being necessary to improve flow properties. Their use will
result in an economic advantage in that less work will be expended at a given
set of processing conditions. In addition, improved product appearance usually
results, particularyly with respect to improved surface appearance. An internal
lubricant will promote fusion.
Other distingguishing characteristics of
internal and external lubricants are the effects they have on fusion time.
Internal lubricants show no change in fusion time as the concentration of
lubricant increases in the polymer system; external lubricants lengthen fusion
time with increasing concentration.
Some lubricants exhibit properties of
both internal and external lubricants and are identified as internal/external.
The degree of each type of lubricity imparted in a specific application is
depending on the type and concentration of lubricant employed, the composition
of the plastic system, the type of processing equipment, and the operating
parameters of the processing system.
In some instances, one encounters
undersiable side effects in the use of lubricants, most notably in the
reduction of heat stability which can lead to such major production problems
as:
Thermal degradation of the thermalplastic
material within the extruder requires a halt of process operations for cleaning
out.
Recycling of materials is limited.
The use of thermoplastic materials in
light colored goods is limited.
High level of expensive heat stabilizers
may be required.
Plasticizers
Plasticizers are added to thermoplasts or elastomers
to make them more flexible, improve processability, or allow them to foamed.
Generally, plasticizers are low-molar-mass liquids, and only seldom are they
low-or high-molar-mass solids. Elastomers are mostly plasticized with mineral
oils: typical rubber tires, for example, contain about 40% mineral oil.Phthalic
esters dominate plasticizers for thermoplasts, and here, di (2-ethyl hexyl)
phthalate (“dioctyl phthalate “, DOP) is the most used.Polymeric plasticizers
are only used in a relatively small number of cases. They are mostly polyesters
or polyethers. High-molar-mass polyesters are used for polymer blends, but
low-molar-mass polyesters are used as actual plasticizers. Since the latter are
produced by polycondensation, they have a broad molar mass distrubution, and
thus monomer and oligomer components. High monomer factions mean low polymer
fraction, but quite high oligomer fractions. In such cases, they are called
oligomeric plasticizers.
A distinction is also made between primary and
secondary plasticizers. Primary plasticizers interact directly with the polymer
chains, where sencondary plasticizers are actually only diluents for the
primary plasticizers. For this reason, secondary plasticizers are also called
extenders. This, depending on the polymers, a given plasticizer can act as
either a primary or a secondary plasticizer. For example, heavy oils are
extenders for PVC, but primary plasticizers for elastomers.
Eighty to eighty-five percent of all plasticizers are
used to produce plasticized PVC. The phthalates are preferentially used to
plasticize certain polyurethanes, polyester resin, and phenolic resin.
Phosphaste esters are good plasticizers for melamine resins, unstaturated
polyesters, phenolic resins, polyamides, and cellulose acetate. A total of
about 500 different plasticizers are commercially available on the market.
Plasticizers incerease the chain segment mobility by
different molecular effects. Polar plasticizers produce the gauche effect with
polar polymer chains, that is, they increase the gauche conformation fraction
at the expense of the trans conformations, and so reduce the mean rotational
energy barrier. Acting as more or less good solvents, plasticizers dissolve
helix structure and crystalline regions. In addtion, chain segments become more
separated on account of the dilution effect. On the other hand, solvation does
not increase chain mobility since a solvent sheath acts like a substituent and
consequently increase the rotational energy barrier.
Because of the increased chain segment mobility, the
glass transition temperatures, moduli of elasticity, tensile strengths, and
hardness are decreased, whereas the extension at break is increased. The change
in these parameters can thus be used as a macroscopic meaure of the effectivity
of the plasticization. Of these parameters, only the glass transition
temperature depends solely on the polymer chain mobililty, all other parameters
contain contributions from other effects. Thus, measurements on plasticization
effectively using glass transition temperatures, moduli of elasticity, tensile
strengths, elongations at break, and hardness can not yield identical results.
To increase segment mobility, the plasticizer must be
able to form a thermodynamically stable mixture with the polymer, that is, it
must be compatible with the polymer, but solvents which are too good stifffen
the chain by solvation. Thus, plasticizers must be solvents which are as poor
as possible.
Stabilizers
Stabilizers
provide protection against degradation caused by heat, oxidation, and solar
radiation. Thus, when used in plastic compositions they may be classified as
heat (or thermal) stabilizers, antioxidants and UV light stabilizers.
It is the role of heat stabilizers to prevent the
polymer from degrading during the short period of high temperature (150℃ to 300℃) processing
and to protect the finished plastic article against slow aging over longer
periods at service temperatures.
Antioxidants inhibit or retard oxidative degradation
at normal or elevated temperatures during processing, storage or service. Most
polymers undergo some oxidation degradation, but hydrocarbon polymers are
specially susceptible.Antioxidants, therefore, are generally added in small
quantities.
Most plastics exhibit varying degrees of degradation
upon prolonged outdoor exposure. Polypropylene, poly (vinyl chloride),
polyethylene, polyesters, crstalline and high impact polystyrenes, and ABS are
particularyly sensitive. Other plastics, particularly poly (methyl
methacrylate) and the fluorocarbons, are much more resistant. To arrest or
retard polymer degradation caused by the ultraviolet portion of solar
radiation, plastic formulations contain UV absorbers. These are compounds such
as substituted benzophenones, benzotriazoles and acrylonitriles that
selectively absorb harmful radiation and convert it to heat energy.
Pigments such as titanium dioxide and zinc oxide are
also used to protect plastics against the harmful effect of ultraviolet
radiation.
They function by absorbing some UV radiation, but
their ability to reflect radiation (heat as well as light) accounts for much of
their effectiveness.In applications where colour is not a requirement, carbon
black, which absorb UV light, is widely used as a very effective stabilizer
(e.g. in black polyethylene).
2014年10月6日星期一
PVC Additives (2)
3. FILLERS
Essentially fillers are added to formulations to
reduce costs, although they may offer other advantages – such as opacity,
resistance to blocking, reduced plate-out, improved dry blending. On the other
side, fillers can reduce tensile and tear strength, reduce elongation, cause
stress whitening, reduce low temperature perforance.
The most common fillers used with PVC are calcined
clays, and water-ground and precipitated calcium carbonates of particle size
around 3 micrometers. Other fillers are silicas and talcs.
4. LUBRICANTS
These materials are of prime importance in
PVC processing. They are decribed below.
⑴ Improve the internal flow characteristics
of the compound.
⑵ Reduce the tendency for the compound to
stick to the process machinery
⑶ Improve the surface smoothness of the
finished product
⑷ Improve heat stability by lowering
internal and/or external friction
Examples of lubricants, with which
you may be familiar, are stearic acid, calcium stearate, Wax E, polythylene AC
617.
5. PROCESSING AIDS
These may be regarded as low-melt viscosity,
compatable solid plasticizers. They are added to lower processing temperatue,
improve roll release on calenders, reduce plate-out, promote fusion.
They are usually added at concentration of 5.0%. The
most widely used processing aids are acylic resins of which acrylic K 120N is
an example.
6. OTHER ADDITIVES
There are
several other addtives which we will list and comment on briefly.
⑴ Impact Modifiers: These are usd in rigid
vinyls to improve impact resistance. These are usually acrylic or ABS polymers
used at 10-15 phr levels. Examples are Kureha BTA 111, Blendex 301.
⑵ Light Stabilizers: for resistance to
ultraviolet radiation. They are used in low concentrations 0.5-1.5 phr.
⑶ Flame Retardants: PVC is inherently
self-extinguishing However, the plasticizers and additives are not. Therefore,
flame retardants are added. The most widely known one is antimon tri-oxide.
⑷ Anti-Static Agents
⑸ Fungicides: Vinyzene BP-5
⑹ Foaming Agents: Chemicals that decompose
at predetermined temperature to produce a certain volume of gas within the
molten vinyl and thereby create foam.
⑺ Colorants: Both pigments and dyes can be
used. However, dyes, which are soluble organic substances,are used sparingly de
to their tendency toward migration and extract ability. Heat resistance of
colorants must be carefully evaluated.
In summary, we have seen that a vinyl
compound consists of following components: PVC resin, plasticizer, heat
stabilizer, lubricant, special additive, colorants.
PVC Additives (1)
It should be noted that PVC resin, of themselves, are
of no practical use. When fused, they are hard, brittle compounds. Their
inherent limited heat stability make any type of processing difficult if not
impossible. Therefore, in order to produce a useful product other ingredient
are added to the PVC resin for the purpose of : increasing flexibility,
providing adequate heat stability, improving processability, imparting
aesthetic appeal.
Let’s consider these ingredients in some detail.
1.
PLASTICIZERS
Plasticizers are low boiling liquids or low molecular weight solids that
are added to resins to alter processing and physical properties. They increase
resin flexibility, softness and elongation. They increase low temperature
flexibility but decrease hardness. They also reduce processing, temperatures
and melt viscosity in the case of calenering.
Plasticizers fall into two categories based on their solvating power and
compatibility with resins.
A.
Primary
Plasticizers: are able to solvate resins and retain compatibility on aging.
Samples of these would be:
DOP Dioctyl phthalate
S-711 Di(n-hexyl; n-octyl; n-decyl) phthlate
(linear)
DIDP Di-iso decyl phthate
B.
Secondary
Plasticizers: are so defined because of their limited solubility and
compatibility and are, therefore, used only in conjunction with primary
plasticizers. The ratio of primary to secondary depends on the type and
quantity of the particular plasticizers. Secondary plasticizers are used to
impart special properties such as:
-low temperature flexibility DMODA (di-normal octyl decyl adipate)
DOZ (di-octyl azelate)
DOA (di-octyl adipate)
-
Flame retardance Reofas 65 (tri-iso propyl phenyl phosphate)
-
Electrical
properties t tri-mellitates
-
Cost reduction Cereclor, chlorinated parafins
In a separate category are the polymeric
plasticizers. These are long chain molecules and are made from adipic, azelaic,
sebacic, acids and propylene and butylene glycols. The efficiency of polymerics
is poor but volatility and migration are superior. An example of a polymeric
plasticizer is Paraplex G-54.
The characteristics sought in
plasticizers can be summarized as follows:
⑴ efficiency- This is the level or
concentration needed to give a stated hardness, flexibility or modulus.
⑵ the effect on low temperature flexibility.
⑶ solvating power: This influence the
fluxing rate of the compound at a given temperature or at a minimum fluxing
temperature.
The fluxing rate relates directly
to processing time.
Performance: This relates to
volatility, extraction resistance, compatibility.
2.
HEAT
STABILIZERS
The chief purpose of a heat stabilizer is to prevent discoloration
during processing of the resin compound. Degradation begins with the evolution
of Hydrogen Chloride, at about 200 ℉ increasing sharply with time and temperature. Color changes parallel the
amount of degradation running from white to yellow to brown to black.
Therefore, the need for heat stabilizers.
The most effective stabilziers have been
found to be:
⑴ Metal soaps: Barium-cadmium solids and liquids:
Mark 725, Mark 311
⑵ Organo tin compounds: octyl tin mercaptide: Mark
OTM
⑶ Epoxies: epoxidized soya oil (G-62)
The above are most likely most effectively
only when used in combination (synergism).
What are some of the criteria in choosing a
stabilzier system?
⑴ The ability to prevent discoloration
⑵ The amount of lubrication involved. In calandering
this can be of critical importance. Mark 725 has low lubricating effect while
Mark 311 contributes high lubrication effect.
⑶ Plate-Out- a potential side-affect of processing
and has been linked to certain barium-cadium stabilizers.
⑷ Compatability with the resin system- for obvious
reasons.
⑸ Resistance to sunlight staining: atmospheric
discoloration.
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