Purfication Adsorbents

Company Profile

 

 

Shandong Synergy Tech Co., Ltd is a leading manufacturer of chemical materials, adsorbents, desiccants, and catalysts in Petroleum and petrochemical industry. Our company, founded in 2015, is situated in Zibo, Shandong, a renowned city for its classical heavy industries. We operate on a 30 mu area, with a registered capital of 16 million yuan and a dedicated team of 115 employees, including 6 senior engineers and 10 technical engineers.
At our company, we are committed to the development and production of the most advanced, reliable, and cost-effective materials, catalysts and adsorbents. We have successfully established partnerships with renowned international companies such as China National Petroleum Corporation, Sinopec, and Petrochemical Industry Companies from Germany, Britain, Kuwait, Saudi Arabia, Jordan, South Korea, New Zealand, Thailand, Indonesia, the Philippines, and other countries worldwide.

 

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High quality

Our products are manufactured or executed to very high standards, using the finest materials and manufacturing processes.

 

 

Professional team

Our professional team collaborate and communicate effectively with one another, and are committed to delivering high-quality results. They are capable of handling complex challenges and projects that require their specialized expertise and experience.

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The long-term warranty is designed to give consumers more confidence that their purchases and services will continue to be valid.

 

Rich experience

Dedicated to strict quality control and attentive customer service, our experienced staff is always available to discuss your requirements and ensure complete customer satisfaction.

 

 
Purfication Adsorbents of includes the following products
 

Paraffin Separation Adsorbents

Paraffin Separation Adsorbents

 

What Is Paraffin Separation Adsorbents

Paraffin separation adsorbents can be proposed in PSA (Pressure Swing Adsorption) gas phase, as well as in TIP (Total Izomerization Process) and Isosiv units. The target of these units is to boost the octane number of the C5-C6 isomerization unit by recycling the non-converted n-paraffins upstream of the unit.

 

Equilibrium and kinetic gas adsorption behaviors

 

 

Single-component equilibrium adsorption isotherms of C2-C4 olefins and paraffins were collected at different temperatures (273–323 K). illustrated the step-wise adsorption behavior of C2-C4 olefins, which can be attributed to the structural adaptability of flexible MOFs under guest stimuli30,37,39,46,47. At 1.0 bar, the C2H4 uptake reached 31.43 cm3 g−1 and 29.31 cm3 g−1 at 273 K and 298 K, respectively. Similarly, the adsorption capacity for C3H6 was measured to be 33.90 and 27.50 cm3 g−1 at 273 K and 298 K, respectively . Meanwhile, BFFOUR-Cu-dpds could adsorb 21.49 cm3 g−1 n-butene (n-C4H8) at 298 K, which increased to 24.54 cm3 g−1 at 283 K (Fig. 2c and Supplementary Fig. 18a). Note that C2-C4 paraffins, i.e., C2H6, C3H8, and n-butane (n-C4H10), were completely excluded by activated BFFOUR-Cu-dpds even at higher temperatures . Correspondingly, based on the experimental pore volume, the packing density of C2H4, C3H6, and n-C4H8 in BFFOUR-Cu-dpds achieved 471.47 g L−1, 653.92 g L−1, and 680.51 g L−1 at 298 K and 1.0 bar, which was 414.3, 383.1, and 298.8 times higher than the density of gaseous C2H4 (1.138 g L−1), C3H6 (1.707 g L−1), and n-C4H8 (2.276 g L−1) under similar conditions17,48. The time-dependent kinetic adsorption curves at 0.5 bar revealed an abrupt uptake point in <1 min for C2-C4 olefins and quickly reached equilibrium at ~13 min . The kinetic adsorption capacity of C2H4 (25.0 cm3 g−1), C3H6 (24.1 cm3 g−1), and n-C4H8 (14.7 cm3 g−1) was in good agreement with their corresponding equilibrium adsorption capacities. Meanwhile, no noticeable adsorption uptakes were observed on C2-C4 paraffins even after a prolonged period of ~70 mins. The kinetic adsorption curves at 1.0 bar showed a similar phenomenon.

 

Separation selectivity and adsorption enthalpy

Ideal adsorbed solution theory (IAST) was applied to estimate the separation selectivity for C2-C4 olefins/paraffins (0.5/0.5, v/v). The dual-site Langmuir-Freundlich (DLSF) model was employed to fit the adsorption isotherms with remarkable precision . Due to the stepwise adsorption behaviors, the IAST selectivity curves of C2-C4 olefins/paraffins exhibited an increasing trend along the increase of adsorption amounts 51. Specifically, BFFOUR-Cu-dpds showed a high IAST selectivity for C2H4/C2H6 (68.8), C3H6/C3H8 (108.4), and n-C4H8/n-C4H10 (22.9) at 298 K and 1.0 bar, surpassing many leading adsorbents such as Ni-gallate (16.8 for C2H4/C2H6), NOTT-300 (48.7 for C2H4/C2H6), ZnAtzPO4 (12.4 for C2H4/C2H6), Fe2(m-dobdc) (60 for C3H6/C3H8), and Fe2(dobdc) (14.7 for C3H6/C3H8)26,52,53,54,55. To avoid the overestimation of separation performances in molecular-sieving adsorbents by IAST calculations, an intuitive evaluation based on the olefin-to-paraffin uptake ratio was employed23,56,57,58,59. including HIAM-301 (11.47 for C3H6/C3H8), Co-gallate (10.87 for C2H4/C2H6) and JNU-3 (1.21 for C3H6/C3H8), NOTT-300 (5.03 for C2H4/C2H6)11,27,48,52. Although the scarcity of reported data, the uptake ratio for n-C4H8/n-C4H10 also surpassed monolayer AgNO3/SiO2 sorbent (8.33) and Ag+ ion impregnated clay (2.97)60,61. To the best of our knowledge, BFFOUR-Cu-dpds represents the example of simultaneous sieving of C2-C4 olefins and paraffins.

Paraffin Separation Adsorbents

Breakthrough experiments for olefin/paraffin separations

 

 

Dynamic breakthrough experiments were conducted on BFFOUR-Cu-dpds columns using binary gas-mixtures of olefin/paraffin (0.5/0.5, v/v) at 298 K to confirm its practical separation performances . BFFOUR-Cu-dpds demonstrated efficient separations of C2-C4 olefin/paraffin binary gas-mixtures within a single adsorption column. For the gas-mixture of C2H4/C2H6 (0.5/0.5, v/v), C2H6 was rapidly eluted from the column at a flow rate of 1.0 mL min−1, while C2H4 exhibited substantial retention in the column for 28 min until saturation . Notably, the efficient C2H4/C2H6 separation was also obtained despite slightly decreased retention time under humid conditions (RH = 61.9%). Similarly, both C3H8 and n-C4H10 immediately broke through the column, whereas C3H6 and n-C4H8 were detected at retention times of 32.2 min and 21 min, respectively . Considering that the IAST selectivity and uptake ratio are determined by equilibrium effect, the dynamic selectivity based on breakthrough curves was calculated to be 9.16, 8.76, and 3.18 for equimolar C2H4/C2H6, C3H6/C3H8, and n-C4H8/n-C4H10, respectively. These values demonstrate comparable performance to top-ranking adsorbents, such as NUS-6(Hf)-Ag (4.4 for C2H4/C2H6)71, ZJU-75a (14.7 for C3H6/C3H8)72, Y-abtc (8.3 for C3H6/C3H8)73 and KAUST-7 (12.0 for C3H6/C3H8)8. The dynamic adsorption capacity for C2H4, C3H6, and n-C4H8 were calculated to be 17.05 cm3 g−1, 19.97 cm3 g−1, and 14.43 cm3 g−1 respectively, which closely matched their static adsorption amounts at 0.5 bar. Furthermore, clean separations of C2H4/C2H6 and C3H6/C3H8 could also be achieved at higher flow rates of 2.0 and 4.0 mL min−1 . Note that facile adsorbent regeneration was a critical process to obtain high-purity olefins. After reaching the breakthrough point, the column was purged with He sweeping at 5 mL min−1 and 333 K . The productivity of C2H4 and C3H6 with ≥99.5% purity was calculated to be 11.92 L kg−1 and 14.19 L kg−1 in a single adsorption-desorption cycle, which was comparable to the top-ranking adsorbents including UTSA-280 (22.08 L kg−1 99.2% C2H4)17, NOTT-300 (19.66 L kg−1 99.2% C2H4)52, KAUST-7 (10.7 L kg−1 98.3% C3H6)8, and Co-gallate (14.9 L kg−1 98.7% C3H6)11. Meanwhile, the productivity of n-C4H8 was estimated to be 7.4 L kg−1 with ≥90% purity.

Paraffin Separation Adsorbents

 

Breakthrough experiments for olefin/paraffin separations

Dynamic breakthrough experiments were conducted on BFFOUR-Cu-dpds columns using binary gas-mixtures of olefin/paraffin (0.5/0.5, v/v) at 298 K to confirm its practical separation performances . BFFOUR-Cu-dpds demonstrated efficient separations of C2-C4 olefin/paraffin binary gas-mixtures within a single adsorption column. For the gas-mixture of C2H4/C2H6 (0.5/0.5, v/v), C2H6 was rapidly eluted from the column at a flow rate of 1.0 mL min−1, while C2H4 exhibited substantial retention in the column for 28 min until saturation . Notably, the efficient C2H4/C2H6 separation was also obtained despite slightly decreased retention time under humid conditions (RH = 61.9%). Similarly, both C3H8 and n-C4H10 immediately broke through the column, whereas C3H6 and n-C4H8 were detected at retention times of 32.2 min and 21 min, respectively . Considering that the IAST selectivity and uptake ratio are determined by equilibrium effect, the dynamic selectivity based on breakthrough curves was calculated to be 9.16, 8.76, and 3.18 for equimolar C2H4/C2H6, C3H6/C3H8, and n-C4H8/n-C4H10, respectively. These values demonstrate comparable performance to top-ranking adsorbents, such as NUS-6(Hf)-Ag (4.4 for C2H4/C2H6)71, ZJU-75a (14.7 for C3H6/C3H8)72, Y-abtc (8.3 for C3H6/C3H8)73 and KAUST-7 (12.0 for C3H6/C3H8)8. The dynamic adsorption capacity for C2H4, C3H6, and n-C4H8 were calculated to be 17.05 cm3 g−1, 19.97 cm3 g−1, and 14.43 cm3 g−1 respectively, which closely matched their static adsorption amounts at 0.5 bar. Furthermore, clean separations of C2H4/C2H6 and C3H6/C3H8 could also be achieved at higher flow rates of 2.0 and 4.0 mL min−1 . Note that facile adsorbent regeneration was a critical process to obtain high-purity olefins. After reaching the breakthrough point, the column was purged with He sweeping at 5 mL min−1 and 333 K . The productivity of C2H4 and C3H6 with ≥99.5% purity was calculated to be 11.92 L kg−1 and 14.19 L kg−1 in a single adsorption-desorption cycle, which was comparable to the top-ranking adsorbents including UTSA-280 (22.08 L kg−1 99.2% C2H4)17, NOTT-300 (19.66 L kg−1 99.2% C2H4)52, KAUST-7 (10.7 L kg−1 98.3% C3H6)8, and Co-gallate (14.9 L kg−1 98.7% C3H6)11. Meanwhile, the productivity of n-C4H8 was estimated to be 7.4 L kg−1 with ≥90% purity .

Paraffin Separation Adsorbents of Summary

 

 

Light olefins are the precursors of all modern-day plastics. Olefin is always mixed with paraffins in the time of production, and therefore it needs to be separated from paraffins to produce polymer-grade olefin. The state-of-the-art separation technique, cryogenic distillation, is highly expensive and hazardous. Adsorption could be a novel, sustainable, and inexpensive separation strategy, provided a suitable adsorbent can be designed. There are different types of mechanisms that were harnessed for the separation of olefins by adsorption, and in this review, we have focused our discussion on those mechanisms. These mechanisms include,
●Affinity-based separation, like pi complexation and hydrogen bonding,
●Separation based on pore size and shape, like size-exclusion and gate-opening effect,
●Non-equilibrium separation, like kinetic separation. In this review, we have elaborated each of the separation strategies from the fundamental level and explained their roles in the separation processes of different types of paraffins and olefins.

 
The Using Steps of Paraffin Separation Adsorbents

The steps involved in each cycle were as follows:

Pressurization with the feed gas (mixture of 50% olefin and 50% paraffin on mo- lar basis).

High-pressure adsorption with feed gas, that is, feedstep.

High-pressure cocurrent purge with part of the olefin-rich product obtained in step.

Countercurrent.

 

Hydrofining Catalyst
 
Hydrofining Catalyst

 

What Is Hydrofining Catalyst

Lube oil hydrofining is a catalytic technology to prepare lube base stocks for further processing or it may be used as a base-stock finishing step. The process is usually integrated Exol N technology, into an Exolfining configuration, to treat the waxy raffinate from extraction upstream from the lube dewaxing unit.

 

Catalyst and process for hydrofining petroleum wax

A catalyst and process are described for hydrofining petroleum wax comprising contacting the wax with hydrogen in the presence of a catalyst comprising at least one metal hydrogenating component on a porous alumina/silica carrier containing from about 0.2 to 5 wt.% of an alkali metal component. The catalyst has a specific surface area of about 200 to 300 m/sup 2//g and has the following characteristics:
●Volume of pores having a diameter in the range of 60 to 150 a is greater than 80% of the volume of pores having a diameter in the range of 0 to 150 a.
●Volume of pores having a diameter in the range of 0 to 600 a is in the range of about 0.45 to 0.60 ml.

Hydrofining Catalyst

 

Hydrotreating in Petroleum Processing

 

 

Hydrotreating or catalytic hydrogen treating removes objectionable materials from petroleum fractions by selectively reacting these materials with hydrogen in a reactor at relatively high temperatures and at moderate pressures. These objectionable materials include, but are not solely limited to, sulfur, nitrogen, olefins, and aromatics. The lighter distillates, such as naphtha, are generally treated for subsequent processing in catalytic reforming units, and the heavier distillates, ranging from jet fuels to heavy vacuum gas oils, are treated to meet strict product quality specifications or for use as feedstocks elsewhere in the refinery.

 

Hydrofining Catalyst of Features

 

 

Modified Al2O3 as a carrier, the special manufacturing technique ensures the uniform dispersion of active components Co and Mo.
Good hydrogenation activity and stability in activity; simultaneously exhibits excellent hydrodesulfurization, hydrodenitrogenation and olefin saturation abilities.
Adaptable to operating condition fluctuation, good operation flexibility, long service life.

 

Hydrofining Catalyst of Role
Apply to the desulfurization and denitrogenation processes of naphtha.

Apply to the desulfurization and denitrogenation processes of kerosene.

Apply to the hydrofining pretreatment of reforming feedstock.

 

PRODUCT BASIC INFO

Operating temperature/℃

260~380

Pressure/MPa

1.0~8.0

Volume space velocity/h-1

2.0~12.0

Hydrogen oil ratio

100~600

 

PRODUCT SPECIFICATION

Color and shape

Faint yellow, clover extrudate

Size/mm

Φ1.2/Φ1.6/Φ2.0/Φ2.5

Active components

Ni-Mo

Bulk density/(kg.L-1)

0.65~0.75

Crushing strength/(N.cm-1)

≥150

 

Hydrofining Catalyst

 

Process for activating a hydrotreating catalyst

He invention pertains to a process for activating an hydrotreating catalyst comprising a Group VIB metal oxide and a Group VIII metal oxide which process comprises contacting the catalyst with an acid and an organic additive which has a boiling point in the range of 80-500° C. and a solubility in water of at least 5 grams per liter (20° C., atmospheric pressure), optionally followed by drying under such conditions that at least 50% of the additive is maintained in the catalyst. The hydrotreating catalyst may be a fresh hydrotreating catalyst or a used hydrotreating catalyst which has been regenerated.

 

Chloride Removal
 

 

What Is Deoxidizer

The deoxidizer is used in food packaging to reduce the oxygen content in the package and to extend the shelf life. There are various functions of deoxidizer on the market, such as deodorization and moisture absorption, but its main function is still deoxidizer.

Palladium Catalyst

By Deoxidation Methods

 

 

Unavoidably, there will be part of ferric oxide left in molten steel during the smelting process, which reduce the steel quality. Thus, deoxidation is needed during the ingot casting. The steel made by different deoxidation methods has various properties. Therefore, there is rimmed steel, fully-killed steel, and semi-killed (or semi-deoxidized) steel.


Rimmed Steel
It is the unkilled only by ferromanganese, a weak deoxidizer. Because the remained FeO in the molten steel can generate CO with C, there are a lot of foams in the process of casting ingot, like boil, known as rimmed steel. Its organization is not dense enough and contains foams, so the quality is poor; but the rate of finished products is high and the cost is low.


Fully-killed Steel
This kind of steel is deoxidized thoroughly with a certain amount of silicon, manganese, and aluminum deoxidizers. Because deoxidation is thorough, the molten steel can solidify calmly in ingot casting, known as fully-killed steel. Its organization is dense, chemical elements are even, and properties are stable, so its quality is good. However, the productivity is low, so the cost is high. It can be employed in the steel structures used to bear impacts, vibration or important welding.


Semi-killed Steel
Its deoxidation degree and quality are between the above two.

What is the difference between deoxidizer and reductant

 

Function

Deoxidizer is used to remove oxygen from metals and alloys, while reductant is used to reduce the oxidation state of a compound.

01

Application

Deoxidizer is used in metallurgy and welding, while reductant is used in chemistry and industrial processes.

02

Target

Deoxidizer targets oxygen specifically, while reductant can target other elements as well.

03

Reaction

Deoxidizer undergoes oxidation itself, while reductant undergoes reduction.

04

Examples

Deoxidizer is commonly used in steelmaking, while reductant is commonly used in organic chemistry.

05

Palladium Catalyst

What are the different types of Deoxidizers

 

There are three primary elements that manufacturers use as deoxidizers: manganese, silicone and aluminum. Occasionally they also use titanium or zirconium. Manganese, along with providing reliable deoxidizing capabilities, also increases strength in the completed weld.

What does a deoxidizer do

 

Corrosion occurs when bare aluminum is exposed to oxygen and moisture. Extended time in a deoxidizer will remove and inhibit further corrosion of the metal. Chemical processes common to preparing the metal for such surface finishing as anodizing, plating or painting put aluminum at risk for corrosion.

Palladium Catalyst
 
Our Factory
 

Shandong Synergy Tech Co., Ltd is a leading manufacturer of chemical materials, adsorbents, desiccants, and catalysts in Petroleum and petrochemical industry. Our company, founded in 2015, is situated in Zibo, Shandong, a renowned city for its classical heavy industries. We operate on a 30 mu area, with a registered capital of 16 million yuan and a dedicated team of 115 employees, including 6 senior engineers and 10 technical engineers.

 

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FAQ
 
 

Q: What does a deoxidizer do?

A: Deoxidizers work by acting as scavengers that combine with oxygen and then, as the weld metal cools, they diffuse with the oxygen to the surface of the weld.

Q: What are the examples of deoxidizing agent?

A: Below is a list of commonly used metallic deoxidizers: Ferrosilicon, ferromanganese, calcium silicide - used in steelmaking in production of carbon steels, stainless steels, and other ferrous alloys. Manganese - used in steelmaking. Silicon carbide, calcium carbide - used as ladle deoxidizer in steel production.

Q: What is the meaning of deoxidizing?

A: To remove oxygen atoms from (a compound, molecule, etc)

Q: What is Deoxidizer made of?

A: The solutions based on nitric, sulfuric, or chromic acids are most commonly used for the deoxidation of aluminum. The nitric acid and sulfuric acid-based solutions are interchangeably used as deoxidizers. As nitric acid is most commonly used so in this article nitric acid-based solutions are discussed in detail.

Q: What do Deoxidizers remove from a weld?

A: How do deoxidizers remove oxygen from the weld zone. Deoxidizers work by acting as scavengers that combine with oxygen and then, as the weld metal cools, they diffuse with the oxygen to the surface of the weld.

Q: What are Deoxidizers used for?

A: A deoxidizer is a compound used in a reaction to remove oxygen. These products contain one or more elements that are scavengers for oxygen decreasing the presence of dissolved oxygen in molten metal. Degasifiers can remove oxygen and other unwanted gases such as hydrogen as well.

Q: What is a hydrotreating catalyst?

A: Catalytic hydrotreating is a hydrogenation process used to remove about 90% of contaminants such as nitrogen, sulfur, oxygen, and metals from liquid petroleum fractions. These contaminants can have detrimental effects on the equipment, the catalysts, and the quality of the finished product.

Q: What is hydroprocessing catalyst?

A: Hydroprocessing is a catalytic term relating to the processes of hydrocracking and hydrotreating. These process are for the removal of sulfur, oxygen, nitrogen and metals from crude oil, this is done in the refining of fuel to enable lower sulfur levels in fuels.

Q: What are the catalysts for hydrocracking?

A: The catalysts used in hydrocracking are all of the bifunctional type, combining an acid function and a hydrogenating function. The acid function is carried by supports with a large surface area and having a superficial acidity, such as halogenated aluminas, zeolites, amorphous silica-aluminas, and clays.

Q: What is the meaning of Hydrorefining?

A: A process for improving the quality of gasoline and other petroleum products by treating with hydrogen in the presence of a catalyst at a temperature below that at which decomposition takes place compare hydroforming.

Q: What is the process of Hydrofining?

A: A hydrofining process in which a sulfur- and hydrocarbon-containing processing stream is supplied to a multi-stage hydrotreating reactor incorporating separate stages of cobalt molybdenum catalysts. Hydrogen may be supplied concurrently or counter-currently with the hydrocarbon-containing processing stream.

Q: Why do we need hydrotreating?

A: Hydrotreating processes are standard in refineries primarily to remove sulfur from refined petroleum fuels. This helps reduce sulfur dioxide emissions that are formed when the fuels are combusted.

Q: Is hydrocracking the same as catalytic cracking?

A: The basis of catalytic cracking is carbon rejection, while hydrocracking is a hydrogen addition process. Catalyst cracking uses an acid catalyst, while hydrocracking uses a metal catalyst on acid support. Another differnce is that catalyst cracking is an endothermic process while hydrocracking is an exothermic process.

Q: What are the examples of hydroprocessing catalysts?

A: Transition metal sulfides are the most prominent materials in hydroprocessing catalysis. The traditional catalysts for hydrotreating are the sulfided combinations of alumina-supported Mo or W promoted by Co or Ni; CoMo/Al2O3, NiMo/Al2O3, and Ni(Mo)W/Al2O3 being the most common commercial examples[19,22].

Q: Is hydrocracking the catalytic splitting in petroleum refining?

A: In petroleum refining, hydrocracking is the catalytic splitting and addition of H2 to large hydrocarbon molecules and the resultant production of smaller, more volatile, and more saturated molecules.

Q: What are the best solvents for catalytic hydrogenation?

A: Alcohols (e.g., methanol or ethanol) are the most widely used solvents for reported heterogeneous catalytic hydrogenation reactions [21]. Wei et al. [22] have shown that Pd catalysts exhibit higher activity for hydrogenation reactions in toluene and ethanol, than in DMF, acetonitrile, or water.

Q: What are the benefits of hydrocracking?

A: Catalytic Hydrocracking | FSC 432: Petroleum Refining
As a hydrogen-addition process, hydrocracking provides high yields of valuable distillates without producing low-grade byproducts (e.g., heavy oils, gas, or coke) as experienced in carbon rejection processes such as coking.

Q: How does hydrotreating work?

A: In the hydrotreating process, the feed stream is pressurized, heated, and combined with hydrogen and then fed to a reactor. In the reactor, the hydrogen reacts with sulfur and nitrogen bearing species and forms H2S and/or NH3. These compounds are then removed in the stripper column.

Q: What is the process of pre sulfiding?

A: The presulfiding agent decomposes in the hydrogen atmosphere under heat with the catalysts and sulfur combines with hydrogen to form hydrogen sulfide, which serves as the medium to react the sulfur with the metallic surfaces of the catalyst.

Q: How does hydrocracking work?

A: A hydrocracking unit, or hydrocracker, takes gas oil, which is heavier and has a higher boiling range than distillate fuel oil, and cracks the heavy molecules into distillate and gasoline in the presence of hydrogen and a catalyst.

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Paraffin Separation Adsorbents, 5A molecular sieve spheres for alkyl benzene molex unit, adsobents for Hydrodesulfurization