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  • Polymer Deodorizing Agents: Enhancing Material Quality and Environmental Comfort

    Polymer Deodorizing Agents: Enhancing Material Quality and Environmental Comfort

    Polymer deodorizing agents are specialized additives designed to eliminate or reduce unpleasant odors emitted by polymer materials during production, processing, or end-use. As polymers like plastics, rubbers, and composites find widespread use in daily products—from food packaging to automotive parts—controlling their inherent or residual odors has become critical for consumer acceptance and regulatory compliance.
    These agents operate through two primary mechanisms: physical adsorption and chemical neutralization. Physical deodorizers, often based on porous materials like activated carbon, zeolites, or cyclodextrins, trap odor molecules within their microscopic pores, preventing their release into the air. Chemical deodorizers, such as organic amines or metal oxides, react with odor-causing compounds (e.g., volatile organic compounds, sulfur-containing gases) to form non-volatile, odorless byproducts, permanently neutralizing the source of the smell.
    The choice of deodorizing agent depends on the polymer type and odor characteristics. For instance, zeolite-based agents excel in absorbing polar odors in polyolefins, while metal oxide composites are effective against sulfurous smells in rubber products. Modern formulations often combine both mechanisms to tackle complex odor profiles, ensuring broad-spectrum efficiency.
    Applications span diverse industries. In food contact plastics, food-grade deodorizers eliminate residual monomer smells without compromising safety. Automotive interiors use these agents to reduce off-gassing from vinyl or polyurethane components, enhancing cabin air quality. In construction materials like PVC pipes or insulation foams, they mitigate odors during installation and long-term use.
    Key advantages include compatibility with polymer processing conditions (e.g., high temperatures during extrusion), minimal impact on material properties (such as tensile strength or flexibility), and long-lasting performance. Recent advancements focus on eco-friendly formulations, using biodegradable carriers or renewable adsorbents, aligning with global sustainability trends.
    As consumer demand for low-odor, high-quality polymer products grows, the development of efficient, versatile deodorizing agents continues to drive innovation, bridging material functionality with environmental and user comfort.

  • SOLACI SOCIME 2025 | Unlock the Latin American Medical Market and Jointly Build a Global Health Future!

    SOLACI SOCIME 2025 | Unlock the Latin American Medical Market and Jointly Build a Global Health Future!

    The 2025 Annual Congress of the Latin American Society of Interventional Cardiology (SOLACI SOCIME 2025) was grandly held in Mexico from August 6 to 8. As the most influential cardiovascular intervention event in Latin America, SOLACI brought together experts and scholars in the field of cardiovascular intervention from various countries in Latin America and around the world. They jointly discussed and shared the latest research results and clinical experience, making it an important platform for showcasing cutting-edge technologies in global cardiovascular interventional diagnosis and treatment.

    Octoparms® Vena Cava Filter Tanghulu® Balloon MiStent® Coronary Drug-Eluting Stent

    Kossel’s Exhibited Products

    Octoparms® Vena Cava Filters

    In the core exhibition area of this congress, Kossel demonstrated innovative products and professional solutions in the fields of peripheral intervention, coronary intervention, and cardiac electrophysiology. Particularly, its core products that attracted much attention, such as the Octoparms® Vena Cava Filter, Tanghulu® Balloon, and MiStent® Coronary Drug-Eluting Stent, drew the attention of experts and business partners from countries including Mexico, Costa Rica, Panama, Brazil, Peru, and Colombia, who came to observe and communicate.

    Octoparms® Vena Cava Filter Tanghulu® Balloon MiStent® Coronary Drug-Eluting Stent

    We carefully listened to the suggestions and expectations of visitors regarding Kossel’s products, which provided directions for further improving product performance and developing customized services to meet the specific clinical needs in the Latin American region.

    Octoparms® Vena Cava Filter

    Tanghulu® Balloon

    MiStent® Coronary Drug-Eluting

    Through this congress, Kossel further gained insights into the regional national policies, clinical needs, market scale, and other information, and promoted the initiation of local registration. This laid a solid foundation for better serving overseas patients in the Latin American region in the future.

    Going forward, Kossel will continue to deepen its presence in the industry, integrate technologies and experiences from top experts around the world, and conduct innovative R&D. With higher-quality products and services, Kossel will empower clinical practice, benefit a large number of patients, and contribute the strength of a Chinese medical device brand to improving the cardiovascular health level in this region!

  • The Development History of Camlock Couplings

    The Development History of Camlock Couplings

    Camlock couplings, also known as cam and groove fittings, have played an essential role in fluid transfer systems for decades. Their simple yet effective design, combining ease of use with secure connections, has made them indispensable in various industries. From their humble beginnings to their widespread use today, the history of camlock couplings is a testament to the evolution of industrial engineering and technology.

    Early Beginnings: The Quest for Efficient Couplings

    The origins of camlock couplings can be traced back to the mid-20th century when industries began to require more efficient and reliable methods of transferring liquids, gases, and powders. Traditional coupling methods, such as screw-on fittings, were slow and often prone to leaks. As industries such as agriculture, chemical processing, and water treatment expanded, the need for faster, more secure, and more durable connections became urgent.

    The solution came from the development of a coupling system that utilized a cam lever mechanism. This design allowed users to quickly and securely connect hoses or pipes without the need for threading or heavy manual effort. The first camlock couplings were made from durable metals such as aluminum and stainless steel, which provided the necessary strength and corrosion resistance for a wide range of industrial applications.

    Design and Patent: The Birth of the Camlock Coupling

    The breakthrough came in the 1950s when an American engineer named John R. “Jack” Fitzgerald patented the camlock coupling design. Fitzgerald recognized that the traditional methods of securing fittings were inefficient and often resulted in accidents or leakage. His design incorporated a series of cams, or levers, which locked into place over a groove on the coupling. This simple yet effective mechanism allowed the coupling to be easily connected and disconnected, even under high-pressure conditions.

    This innovation quickly gained traction in industries that required frequent assembly and disassembly of hose connections, particularly in fields like firefighting, agriculture, and chemical handling. The ability to easily connect hoses and pipelines saved valuable time, improved safety, and reduced the likelihood of leaks during fluid transfer.

    Growth and Widespread Adoption

    Following Fitzgerald’s patent, the camlock coupling rapidly gained popularity throughout the United States and beyond. The versatility and simplicity of the design allowed it to be used in a wide range of industries, including fuel transfer, construction, mining, and food and beverage manufacturing. The ability to handle various substances—from water to chemicals to petroleum—further boosted its widespread adoption.

    As demand for camlock couplings grew, manufacturers began to produce fittings in a variety of sizes and materials, making them suitable for different applications. Over the years, camlock couplings were manufactured from materials such as brass, stainless steel, aluminum, and even plastic, depending on the specific needs of the industry. The introduction of materials like stainless steel and polypropylene also addressed concerns regarding corrosion and chemical compatibility.

    Innovations in Materials and Design

    The next significant step in the evolution of camlock couplings came with advancements in materials. The development of corrosion-resistant alloys and composite materials allowed camlock couplings to be used in more demanding environments, including those where exposure to harsh chemicals or extreme temperatures was common. This increased the coupling’s application range, making it suitable for industries like oil and gas, water treatment, and pharmaceuticals.

    Moreover, camlock couplings began to be designed with a range of safety features, such as locking pins, vibration resistance, and quick-release mechanisms, further enhancing their safety and usability. As industries continued to grow and diversify, the demand for more specialized camlock fittings emerged. This led to the development of additional features, including sanitary camlocks for food-grade applications, specialized gaskets for sealing, and custom configurations for unique industrial needs.

    Global Expansion and Modern-Day Use

    In the latter half of the 20th century, as globalization increased and international trade expanded, the use of camlock couplings became more prevalent worldwide. Manufacturers in Europe, Asia, and other regions began producing their versions of the camlock coupling, leading to increased competition and innovation in the industry.

    Today, camlock couplings are used across virtually every industry where fluid transfer is required. From firefighting equipment to pharmaceutical production, camlock couplings remain a trusted choice for secure, efficient connections. Modern-day camlock couplings are available in a vast range of sizes, materials, and configurations, ensuring that they meet the specific demands of the most challenging applications.

  • Bulk Plastic Odor Eliminator: A Catalyst for Clean, Safe Plastics

    Bulk Plastic Odor Eliminator: A Catalyst for Clean, Safe Plastics

    In the dynamic landscape of modern manufacturing, Bulk Plastic Odor Eliminator stands as a transformative solution addressing a critical challenge: the persistent, unwanted odors plaguing plastic products. These odors, often stemming from residual chemicals like solvents, plasticizers, and volatile organic compounds (VOCs), not only compromise product quality but also hinder consumer trust and regulatory compliance. By integrating advanced adsorption and neutralization technologies, this innovative formulation ensures large-scale plastic production meets the highest standards of purity and safety.

    Core Technology and Formulations
    Bulk Plastic Odor Eliminators operate through two primary mechanisms. Adsorption-based solutions, such as those containing activated carbon or zeolites, leverage porous structures to physically trap odor molecules. For instance, activated carbon’s high surface area efficiently captures aldehydes, benzene, and formaldehyde, common culprits in plastic off-gassing. **Reaction-based eliminators**, like Ecosorb’s plant oil–derived formulations, chemically neutralize odor-causing compounds. These formulations, free of harmful VOCs, break down volatile molecules into odorless byproducts, ensuring both effectiveness and environmental responsibility.

    Manufacturers also employ specialized formulations like RT-10126, an alkaline compound that chelates harmful substances in recycled plastics while maintaining mechanical integrity. Such tailored solutions highlight the industry’s shift toward precision chemistry, balancing performance with sustainability.

    Diverse Industrial Applications
    The utility of Bulk Plastic Odor Eliminators spans industries:
    – Packaging: Ensures food-grade plastics remain free from taints, safeguarding product integrity and consumer health.
    – Automotive: Eliminates chemical smells in interior components, enhancing driver comfort and aligning with automotive quality benchmarks.
    – Medical Devices: Meets stringent hygiene requirements by neutralizing odors in sterile environments, critical for patient safety.
    – Recycling: Reduces foul odors in reprocessed plastics, expanding their use in applications like textiles and construction.

    For example, a U.S. specialty plastics manufacturer faced neighbor complaints due to mercaptan emissions during production. By deploying Ecosorb 606 via a vapor-phase system, they achieved 95% odor reduction, resolving regulatory issues and maintaining operations. Similarly, a leading plastics producer used VOC collectors with activated carbon to eliminate flammable vapors from their office areas, ensuring worker safety and compliance.

    Advantages Redefining Industry Standards
    1. Efficiency: Acts rapidly, often within minutes, outperforming traditional methods like ventilation or chemical washing, which are time-consuming and resource-intensive.
    2. Safety: Non-toxic formulations (e.g., plant-based Ecosorb, RoHS-compliant RT-10126) ensure compatibility with food packaging, medical devices, and sensitive environments.
    3. Cost-Effectiveness: Reduces operational expenses by minimizing waste and reprocessing needs. For instance, integrating odor eliminators directly into resin during extrusion eliminates post-production treatments.
    4. Sustainability: Supports circular economy goals by enhancing the viability of recycled plastics. Technologies like thermal decomposition and vacuum stripping, combined with odor eliminators, make reprocessed materials market-ready.

    Market Dynamics and Future Outlook
    The global odor eliminator market is projected to grow at a 5% CAGR from 2025 to 2033, reaching $9.7 billion by 2033. This growth is driven by:
    – Regulatory Pressures: Stricter EU REACH and U.S. FDA standards mandate VOC reduction, pushing adoption of compliant solutions.
    – Consumer Demand: Health-conscious buyers prioritize odor-free products, particularly in packaging and home goods.
    – Technological Innovation: Enzyme-based formulations and smart sensors are emerging to tackle complex odor challenges in real time.

    Bulk Plastic Odor Eliminators are not merely additives—they are enablers of quality, sustainability, and consumer confidence. By neutralizing harmful compounds at scale, these solutions empower manufacturers to meet regulatory demands, reduce environmental impact, and deliver products that align with modern expectations. As the industry evolves toward greener practices, Bulk Plastic Odor Eliminators will remain indispensable, bridging the gap between efficiency and responsibility. In an era where every molecule matters, this technology ensures plastics leave a positive impression—odorless, durable, and future-ready.

  • Advanced Additives for Industrial VOCs Removal: A Paradigm Shift in Sustainable Emission Control

    Advanced Additives for Industrial VOCs Removal: A Paradigm Shift in Sustainable Emission Control

    Volatile Organic Compounds (VOCs) pose significant environmental and health risks, prompting industries worldwide to adopt innovative solutions. Industrial VOCs removal additives have emerged as a cornerstone of modern emission control, offering efficient, cost-effective, and eco-friendly alternatives to traditional methods. These additives address the challenges of VOC off-gassing in manufacturing, packaging, and transportation, ensuring compliance with stringent regulations while enhancing product quality.

    Mechanisms and Types of VOCs Removal Additives
    VOCs removal additives operate through diverse mechanisms tailored to specific applications. Adsorbents, such as Clariant’s DESVOCANT, utilize naturally occurring bentonite clay to trap VOCs like benzene and formaldehyde in enclosed environments, preventing their release during shipping or storage. This non-toxic solution reduces the need for ventilation and minimizes customer returns due to lingering odors. Catalytic additives, like CAI Performance Additives’ LDV-1035T, employ surfactant-infused carriers to permanently eliminate VOCs during compounding, particularly in polypropylene (PP) and thermoplastic olefin (TPO) formulations used in automotive interiors. These additives achieve near-complete VOC removal while maintaining material integrity.

    Biological additives represent another frontier. For instance, Tween 20, a non-ionic surfactant, enhances the efficiency of biotrickling filters by improving mass transfer and microbial activity, boosting the removal of hydrophobic VOCs like n-hexane by 15–20%. Such innovations highlight the integration of chemistry and biology to tackle complex pollution challenges.

    Advantages Over Traditional Methods
    Compared to conventional techniques like activated carbon adsorption or thermal oxidation, additives offer distinct advantages. They are cost-effective, with minimal energy consumption and low operational costs. For example, in-mold coating (IMC) technology developed by Nippon Paint and Uchihamakasei integrates resin molding and coating processes, reducing CO₂ emissions by 60% and achieving near-zero VOC release. Additives also improve product quality: DESVOCANT’s non-dusting properties make it ideal for light-colored goods, while LDV-1035T eliminates surface blooms in automotive components.

    Moreover, additives align with sustainability goals. The global low-VOC coating additives market is projected to grow at a 5.5% CAGR, reaching $7.2 billion by 2032, driven by regulatory pressures and consumer demand for eco-friendly products. Companies like Imerys leverage mineral fillers (e.g., wollastonite and talc) to reduce resin demand in coatings, lowering VOC content without compromising performance.

    Applications Across Industries
    Industrial sectors are increasingly adopting VOCs removal additives. In automotive manufacturing, IMC technology and catalysts like LDV-1035T ensure compliance with REACH and EPA standards while enabling complex surface finishes. The packaging industry relies on DESVOCANT to mitigate VOC accumulation in enclosed shipments of textiles, furniture, and electronics, safeguarding both workers and end-users. In coating and paints, coalescing agents (e.g., Ox Film 351) and low-VOC defoamers (e.g., Tego Foamex 812) enhance film formation and reduce emissions in water-based formulations.

    Future Directions
    The field is evolving toward smart and sustainable solutions. Nanotechnology-based catalysts and bio-based additives (e.g., microbial-mineral blends) are being explored for higher efficiency and biodegradability. Additionally, hybrid systems—such as UV-ozone technology combined with water scrubbing, which achieves 98.5% VOC removal—demonstrate the potential of integrated approaches.

  • Camlock Couplings in Australia: Understanding the AS Standard

    Camlock couplings are widely used across Australian industries for efficient fluid transfer in mining, agriculture, and industrial applications. Unlike the NPT standard in North America or BSP in the UK, Australia primarily follows the **Australian Standard (AS)** for camlock connections. This article examines the AS standard for camlock couplings, its key specifications, and implementation best practices in the Australian market.

    AS Standard in Australian Camlock Systems

    The Australian Standard AS 2638 governs camlock (quick-release) couplings, ensuring compatibility with domestic industrial equipment. Key standards include:

    1. AS 2638 – Specifies requirements for quick-action couplings (camlock type)
    2. AS 1722 – Covers pipe threads compatible with BSP standards
    3. AS 3688 – Standard for water supply fittings

    Why AS Standard Dominates Australian Market

    1. Compatibility with BSP System – Aligns with British-influenced infrastructure
    2. Rugged Design Requirements – Suits Australia’s harsh operating environments
    3. Water Industry Compliance – Meets strict water authority specifications
    4. Safety Regulations – Complies with Australian Work Health and Safety standards

    AS Standard vs. Other Global Standards

    Parameter AS (Australia) BSP (UK) NPT (USA) JIS (Japan)
    Thread Type BSPP/BSPT BSPP/BSPT NPT PT/PS
    Sealing Washer (BSPP) Washer (BSPP) Taper + sealant Washer/taper
    Pressure Rating 10-25 bar 10-20 bar 15-30 bar 10-20 bar
    Common Materials 316SS, brass Brass, steel Steel, aluminum Brass, steel

     

    Key Distinctions:

    – AS couplings feature heavier construction than standard BSP
    – Unique color-coding requirements for different media
    – Mandatory compliance with Australian safety regulations

     

  • Reference Document | Expert Consensus on Ultrasound Interventional Therapy for Hemodialysis Vascular Access in China (2024 Edition)

    Abstract

    This consensus aims to provide clinical physicians with standardized guidance for ultrasound-guided PTA procedures, offer a reference for healthcare administrators in conducting quality control, and promote the wide application and popularization of ultrasound technology in arteriovenous dialysis access.

    Preoperative ultrasound assessment

    Sequence for ultrasound assessment of autologous AVF
    In the direction of blood flow along the internal fistula, successively evaluate the conditions of the inflow tract artery, the anastomosis site, the fistula vein all the way to the point where it joins the brachiocephalic vein to enter the subclavian vein or where the great saphenous vein joins the axillary vein.

    AVG ultrasonic assessment sequence
    In the direction of blood flow along the internal fistula, successively evaluate the conditions of the inflow tract artery, the arterial anastomosis, the entire segment of the graft, the venous anastomosis, the autologous outflow tract vein up to the point where it joins the brachiocephalic vein to enter the subclavian vein, or where the great saphenous vein joins the axillary vein throughout the entire vascular pathway.

    Evaluation content
    Blood flow volume, resistance index (RI), vascular morphology and structure (including vessel diameter, intima-media thickness, calcification status, vascular course and depth), stenosis location (including vessel diameter, length and peak systolic velocity ratio (PSVR), thrombus condition (including location, nature and amount of thrombus)

    Ultrasound manifestations and assessment indicators of vascular stenosis
    1.Blood flow: Under the condition of stable systemic hemodynamics, the natural blood flow of the autologous arteriovenous fistula (AVF) is less than 500 ml/min, and the natural blood flow of the arteriovenous graft (AVG) is less than 600 ml/min.
    2.Vascular inner diameter: For veins, the inner diameter of local blood vessels ≤ 1.7 mm or the inner diameter of long segments of blood vessels ≤ 2.0 mm, with a length ≥ 20 mm; for arteries, the inner diameter ≤ 2.0 mm; for veins, if the inner diameter is between 1.8 and 2.0 mm or for arteries, if the inner diameter is between 2.0 and 2.5 mm, a comprehensive judgment needs to be made based on the patient’s clinical symptoms, abnormal signs, and the effectiveness of hemodialysis.
    3.RI:RI>0.5;
    4.PSVR:PSVR>4。

    Indications and periods for PTA intervention

    Indications for intervention
    If the ultrasound assessment reveals that there is one or more areas of stenosis, occlusion or thrombosis in the autologous AVF or AVG, and the patient presents with any of the following one or more symptoms, it is recommended to consider performing PTA intervention.
    1.Physical examination findings: The tremor of the internal fistula has significantly weakened or disappeared, while the pulsation has become more pronounced; abnormal results were observed in the arm elevation test and the pulsation enhancement test.
    2.Abnormal blood flow: The pump-controlled blood flow during dialysis remained consistently below 200 ml/min.
    3.Significant increase in venous pressure: Venous pressure ≥ 200 mmHg, or dynamic venous pressure during dialysis continuously ≥ 160 mmHg
    4.Dialysis recirculation rate: Recirculation rate ≥ 15%
    5.Decrease in dialysis adequacy: The index of attack adequacy (Kt/V) has decreased without a clear cause by more than 0.2
    6.Extended bleeding time: After the dialysis treatment, the time required for stopping bleeding at the puncture site significantly increased (more than 20 minutes), and the influence of coagulation function and anticoagulants was excluded.
    7.Increased difficulty in puncture: The puncture operation becomes more challenging due to poor venous filling.

    Intervention timing
    For those meeting the PTA criteria, they should be managed through the specific time surgery. Under the condition that the patient’s vital signs are stable and there are no surgical contraindications, the PTA surgery should be completed within one dialysis period.

    PTA surgical procedure

    Anesthesia method
    It is recommended to use ultrasound-guided brachial plexus nerve block anesthesia.

    Access selection
    The fistula vein approach and the distal arterial approach are the most commonly used approaches for performing PTA surgery on AVF.
    The artificial vascular approach and the autologous vein approach are the most commonly used approaches for performing PTA surgery via the AVG.

    Surgical procedure
    a. Ultrasound-guided puncture
    b. Heparinization is carried out based on the patient’s condition.
    c. Utilizing the ultrasound probe from multiple angles to understand the details of the lesion, display the shape of the lesion opening and the channel, and assist in the passage of the guide wire.
    d. Balloon Dilatation
    ☑Non-compliant high-pressure balloons are the preferred choice for PTA surgery of arteriovenous dialysis access; for stubbornly narrow lesions, ultra-high-pressure balloons or cutting balloons can be selected. Special balloons can be chosen based on the access route to facilitate insertion.
    ☑The diameter of the balloon should be 1 to 2 mm larger than the inner diameter of the adjacent normal blood vessel; if the difference in inner diameters between the stenotic segment and the adjacent normal vessel is large or there is a thrombotic lesion, it can be gradually expanded; the length of the balloon should not exceed the length of the lesion by too much to avoid damaging the normal vessel.
    ☑For multi-site lesions, the dilation sequence in the reverse blood flow direction can be adopted, with priority given to relieving the stenosis of the outflow tract. The duration of a single balloon dilation is generally controlled within 30 to 60 seconds.
    e.Postoperative hemostasis: compression hemostasis, purse-string suture, 8-shaped suture
    f.Postoperative puncture care planning was carried out, and postoperative precautions were informed.

    Standard for successful surgery

    Technical success criteria
    Self-vascularized arteriovenous fistula (AVF) blood flow ≥ 500 ml/min, AVG blood flow ≥ 600 ml/min; RI < 0.5; Residual stenosis rate at the lesion site < 30%, PSVR < 2

    Clinical success criteria
    The internal fistula tremor can be palpated and has recovered or significantly intensified; the dialysis was successful for two consecutive times after the operation, and the pump-controlled blood flow was ≥ 200 ml/min

    Complication identification

    🔘 Hematoma at the puncture site
    🔘 Vascular spasm
    🔘 Vascular dissection
    🔘 Vascular rupture
    🔘 Pseudoaneurysm
    🔘 Acute thrombosis formation
    🔘 Balloon rupture
    🔘 Fracture of the guidewire and catheter

    Thrombosis treatment of dialysis access

    Drug thrombolysis, mechanical thrombectomy through aspiration, and open surgical thrombectomy methods

    The application of ultrasound technology in other surgical procedures

    ☑ If the retraction after balloon dilation exceeds 50%, if the stenosis recurs twice consecutively within a short period of time, if there is a severe dissection or pseudoaneurysm during the operation, etc., stent implantation can be considered, and covered stents are recommended. The clinical data of stent implantation under ultrasound guidance are not yet sufficient, so when choosing ultrasound as the guiding method, caution should be exercised.
    ☑ Ultrasound-guided balloon-assisted maturation technique (BAM) is the first-line treatment for immature arteriovenous fistulas. When choosing the balloon size, caution should be exercised. In case of necessity, gradual dilation can be performed, and contingency plans for vascular rupture should be formulated.
    ☑ PTA should be the initial treatment for cephalic arch stenosis (CAS). This procedure can be performed under the guidance of DSA or ultrasound. However, stent implantation for CAS is not recommended to be done under ultrasound guidance.
    ☑For high-flow arteriovenous fistulas that cause dialysis access-related extremity ischemia syndrome or high-output heart failure, it is recommended to perform ultrasound-guided arteriovenous dialysis access flow-limiting surgery to reduce the blood flow in the fistula.

  • Industrial VOCs Removal Additive: A Key Solution for Cleaner Production

    Industrial VOCs Removal Additive: A Key Solution for Cleaner Production

    Volatile Organic Compounds (VOCs) are a major group of pollutants in industrial emissions. They are released from various industrial processes such as painting, printing, chemical manufacturing, and more. VOCs not only contribute to the formation of smog and ozone in the atmosphere but also pose significant risks to human health, causing respiratory problems, headaches, and in severe cases, even cancer. As environmental regulations become increasingly stringent worldwide, industries are under great pressure to reduce their VOCs emissions. This is where Industrial VOCs Removal Additives come into play.
    These additives are specifically designed to mitigate the release of VOCs. They work through several mechanisms. Some additives act as adsorbents, like certain zeolite – based materials. Zeo Flair series, for example, has a three – dimensional open structure. Zeo Flair 100/110 is a highly active, hydrophobic adsorbent that can effectively and permanently adsorb a wide range of hydrocarbons, solvents, and other toxic and non – toxic substances down to ppm levels, even in the presence of water. It strongly selects and adsorbs a wide range of VOCs/odors from the air based on organic compositions.
    In the automotive industry, VOCs emitted from interior materials such as plastics, carpets, and adhesives are a concern. Aq Fresh, a new additive technology, has been incorporated into nonwovens, coated textiles, and plastics in automotive interior parts. It contains cucurbiturils, barrel – shaped molecules that can tightly bind a wide spectrum of unwanted VOC molecules, significantly reducing VOC and odor emissions.
    Industrial VOCs Removal Additives also find applications in the pharmaceutical industry. 1 – ethyl – 3 – methylimidazolium acetate ((emim)(ac)) has been used to absorb dichloromethane and ethanol, two common pharmaceutical VOCs. The results showed high removal ratios, demonstrating the effectiveness of this ionic – liquid – based additive.
    The benefits of using these additives are numerous. They help industries comply with environmental regulations, avoiding potential fines and reputational damage. From an economic perspective, they can reduce the need for additional handling or “airing out” of products, such as in the case of packaged goods where VOC – related odors might otherwise lead to customer rejects and returns. For example, DES VOCANT, made from a naturally – occurring bentonite clay mineral, helps control and eliminate the accumulation of VOCs from products enclosed in packaging, reducing the need for container ventilation during shipping.
    Moreover, these additives are often non – toxic and easy to handle, and can be disposed of with normal industrial waste in some cases. In the future, with the continuous development of technology, Industrial VOCs Removal Additives are expected to become even more efficient and cost – effective. New materials and formulations will be developed to target a wider range of VOCs and to work under more complex industrial conditions, contributing to a cleaner and more sustainable industrial environment.

  • Meet Kossel Medtech atSOLACI SOCIME 2025

    Meet Kossel Medtech atSOLACI SOCIME 2025 congress
    Welcome to our
    Booth Number: PA#13

    Meet Kossel Medtech atSOLACI SOCIME 2025